Polytrim Solution

Pronunciation: POL-ee-MIX-in/trye-METH-oh-prim
Generic Name: Polymyxin B Sulfate/Trimethoprim
Brand Name: Polytrim
Polytrim Solution is used for:

Treating eye infections caused by certain bacteria.

Polytrim Solution is an antibiotic combination. It works by killing the bacteria.

Do NOT use Polytrim Solution if: you are allergic to any ingredient in Polytrim Solution

Contact your doctor or health care provider right away if any of these apply to you.

Before using Polytrim Solution:

Some medical conditions may interact with Polytrim Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have the blood disease porphyria

Some MEDICINES MAY INTERACT with Polytrim Solution. Because little, if any, of Polytrim Solution is absorbed into the blood, the risk of it interacting with another medicine is low.

Ask your health care provider if Polytrim Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Polytrim Solution:

Use Polytrim Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

To use Polytrim Solution in the eye, first, wash your hands. Tilt your head back. Using your index finger, pull the lower eyelid away from the eye to form a pouch. Drop the medicine into the pouch and gently close your eyes. Immediately use your finger to apply pressure to the inside corner of the eyelid for 1 to 2 minutes. Do not blink. Remove excess medicine around your eye with a clean, dry tissue, being careful not to touch your eye. Wash your hands to remove any medicine that may be on them. To prevent germs from contaminating your medicine, do not touch the applicator tip to any surface, including the eye. Keep the container tightly closed. Do not wear contact lenses while you are using Polytrim Solution. Take care of your contact lenses as directed by the manufacturer. Check with your doctor before you use them. If you miss a dose of Polytrim Solution, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Polytrim Solution.

Important safety information: Be sure to use Polytrim Solution for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future. Long-term or repeated use of Polytrim Solution may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this. If redness, irritation, swelling, or pain continues or worsens, check with your doctor. Polytrim Solution should be used with extreme caution in CHILDREN younger than 2 months old; safety and effectiveness in these children have not been confirmed. PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Polytrim Solution while you are pregnant. It is not known if Polytrim Solution is found in breast milk. If you are or will be breast-feeding while you use Polytrim Solution, check with your doctor. Discuss any possible risks to your baby. Possible side effects of Polytrim Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. No COMMON side effects have been reported with this product. Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); eyelid swelling; increased or persistent redness, irritation, swelling, pain, or tearing of the eye.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Polytrim side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.

Proper storage of Polytrim Solution:

Store Polytrim Solution between 59 and 77 degrees F (15 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Polytrim Solution out of the reach of children and away from pets.

General information: If you have any questions about Polytrim Solution, please talk with your doctor, pharmacist, or other health care provider. Polytrim Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Polytrim Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Polytrim resources Polytrim Side Effects (in more detail) Polytrim Use in Pregnancy & Breastfeeding Polytrim Support Group 0 Reviews for Polytrim - Add your own review/rating Compare Polytrim with other medications Blepharoconjunctivitis Conjunctivitis, Bacterial

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polymyxin B and trimethoprim ophthalmic

Generic Name: polymyxin B and trimethoprim ophthalmic (paw lee MIX in B and try METH oh prim)
Brand Names: Polytrim

What is polymyxin B and trimethoprim ophthalmic?

Polymyxin B and trimethoprim are antibiotics that fight bacteria in the body.

Polymyxin B and trimethoprim ophthalmic (for the eye) is used to treat eye infections caused by bacteria.

Polymyxin B and trimethoprim ophthalmic may also be used for other purposes not listed in this medication guide.

What is the most important information I should know about polymyxin B and trimethoprim ophthalmic? You should not use this medication if you are allergic to polymyxin B or trimethoprim. Wash your hands before using the eye drops.

Do not allow the dropper tip to touch any surface, including the eyes or hands. If the dropper becomes contaminated it could cause an infection in your eye, which can lead to vision loss or serious damage to the eye.

Do not use this medication while you are wearing contact lenses. Polymyxin B and trimethoprim ophthalmic may contain a preservative that can be absorbed by soft contact lenses and cause discoloration. Wait at least 15 minutes after using polymyxin B and trimethoprim ophthalmic before putting your contact lenses in. Stop using this medication and call your doctor at once if you have swelling or redness of your eyelids, eye redness, eye pain, sensitivity to light; or drainage, crusting, or oozing of your eyes or eyelids. What should I discuss with my healthcare provider before using polymyxin B and trimethoprim ophthalmic? You should not use this medication if you are allergic to polymyxin B or trimethoprim. FDA pregnancy category C. This medication may be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether polymyxin B and trimethoprim ophthalmic passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. How should I use polymyxin B and trimethoprim ophthalmic?

Use this medication exactly as prescribed by your doctor. Do not use it in larger amounts or for longer than recommended. Follow the directions on your prescription label.

Wash your hands before using the eye drops.

To apply the eye drops:

Tilt your head back slightly and pull down your lower eyelid. Hold the dropper above the eye with the dropper tip down. Look up and away from the dropper as you squeeze out a drop, then close your eye.

Gently press your finger to the inside corner of the eye (near your nose) for about 1 minute to keep the liquid from draining into your tear duct. If you use more than one drop in the same eye, wait about 5 minutes before putting in the next drop.

Do not allow the dropper tip to touch any surface, including the eyes or hands. If the dropper becomes contaminated it could cause an infection in your eye, which can lead to vision loss or serious damage to the eye.

Do not use the eye drops if the liquid has changed colors or has particles in it. Call your doctor for a new prescription.

Store the drops at room temperature away from heat and moisture. Keep the bottle tightly closed when not in use. What happens if I miss a dose?

Use the missed dose as soon as you remember. If it is almost time for your next dose, wait until then to use the medicine and skip the missed dose. Do not use extra medicine to make up the missed dose.

What happens if I overdose? Seek emergency medical attention if you think you have used too much of this medicine.

An overdose of polymyxin B and trimethoprim ophthalmic is not likely to cause life-threatening symptoms.

What should I avoid while using polymyxin B and trimethoprim ophthalmic? Do not use this medication while you are wearing contact lenses. Polymyxin B anbd trimethoprim ophthalmic may contain a preservative that can be absorbed by soft contact lenses and cause discoloration. Wait at least 15 minutes after using polymyxin B and trimethoprim ophthalmic before putting your contact lenses in.

Avoid using other eye medications that your doctor has not prescribed.

Polymyxin B and trimethoprim ophthalmic side effects Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using this medication and call your doctor at once if you have a serious side effect such as:

swelling or redness of your eyelids;

eye redness, pain, irritation or sensitivity to light; or

drainage, crusting, or oozing of your eyes or eyelids.

Less serious side effects may include:

mild burning, stinging, or itching in your eye;

mild swelling, itching, or redness of your eyelids;

blurred vision;

watery eyes; or

mild skin rash around your eyes.

This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.

Polymyxin B and trimethoprim ophthalmic Dosing Information

Usual Adult Dose for Bacterial Conjunctivitis:

Instill 1 drop in the affected eye(s) every 3 hours (up to 6 doses per day) for 7 to 10 days.

Usual Adult Dose for Blepharoconjunctivitis:

Instill 1 drop in the affected eye(s) every 3 hours (up to 6 doses per day) for 7 to 10 days.

Usual Pediatric Dose for Bacterial Conjunctivitis:

2 months to 18 years: Instill 1 drop in the affected eye(s) every 3 hours (up to 6 doses per day) for 7 to 10 days.

Usual Pediatric Dose for Blepharoconjunctivitis:

2 months to 18 years: Instill 1 drop in the affected eye(s) every 3 hours (up to 6 doses per day) for 7 to 10 days.

What other drugs will affect polymyxin B and trimethoprim ophthalmic?

It is not likely that other drugs you take orally or inject will have an effect on polymyxin B and trimethoprim ophthalmic used in the eyes. But many drugs can interact with each other. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new; medication without telling your doctor.

More polymyxin B and trimethoprim ophthalmic resources Polymyxin B and trimethoprim ophthalmic Dosage Polymyxin B and trimethoprim ophthalmic Use in Pregnancy & Breastfeeding Polymyxin B and trimethoprim ophthalmic Support Group 1 Review for Polymyxin B and trimethoprim - Add your own review/rating Compare polymyxin B and trimethoprim ophthalmic with other medications Blepharoconjunctivitis Conjunctivitis, Bacterial Where can I get more information? Your pharmacist can provide more information about polymyxin B and trimethoprim ophthalmic.

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Polymyxin B Sulfate eent

Class: Antibacterials
VA Class: OT101
CAS Number: 1405-20-5
Brands: AK-Poly-Bac, Cortisporin, Maxitrol, Neosporin, Pediotic, Poly-Pred, Polytrim

Introduction

Antibacterial; polymyxin antibiotic produced by Bacillus polymyxa.a b c d f g h k l

Uses for Polymyxin B Sulfate Bacterial Ophthalmic Infections

Used in fixed combination with other anti-infectives (e.g., bacitracin, neomycin, gramicidin, trimethoprim) for treatment of superficial infections of the eye caused by susceptible bacteria.b e k l

Used in fixed combination with corticosteroids and other anti-infectives in certain bacterial ocular infections.a d h i j

Not indicated for treatment or prophylaxis of ophthalmic neonatorum.e

Bacterial Otic Infections

Used in fixed combination with corticosteroids (with or without other anti-infectives) for treatment of otitis externa caused by susceptible bacteria.c f g

Polymyxin B Sulfate Dosage and Administration Administration

Apply topically to the eye or ear.a b c d e f g h i j k l

Ophthalmic Administration

In fixed combination with other anti-infectives and corticosteroids, apply topically to the eye as an ophthalmic ointment, solution, or suspension.a b e d h i j k l

Not for injection; do not inject subconjunctivally or directly into the anterior chamber of the eye.a b d h j l

Avoid contamination of the preparation container.a b h l

Shake suspension well prior to each use.a h

To treat eyelids, instill into the eye, then close the eye and rub the excess onto the lids and lid margins.h

Otic Administration

In fixed combination with corticosteroids (with or without other anti-infectives), instill into the external ear as an otic solution or suspension.c f g

Otic preparations are not for use in the eye.c g

Clean and dry ear canal prior to administration.c g Lie with the affected ear upward and instill the otic preparation into the ear canal; maintain this position for 5 minutes.c g Repeat procedure if necessary for the opposite ear.c g

Shake suspension well prior to each use.g

Use sparingly to prevent an accumulation of excess debris in the ear canal.f

Dosage

Potency and dosage of polymyxin B sulfate are expressed in terms of polymyxin B activity.f

Pediatric Patients Bacterial Ophthalmic Infections Polymyxin B Sulfate and Trimethoprim Sulfate Ophthalmic Solution

Infants and children ?2 months of age, mild-to-moderate infections: 1 drop into the affected eye(s) every 3 hours, up to 6 doses daily, for 7–10 days.e

Bacterial Otic Infections Polymyxin B and Neomycin Sulfates and Hydrocortisone Otic Solution or Suspension

Children ?2 years of age: 3 drops into the affected ear(s) 3 or 4 times daily for up to 10 days.c g

Alternatively, insert a cotton wick that has been saturated with the otic preparation into the ear canal; keep the wick moist by adding additional drug every 4 hours.c g Replace the wick at least once every 24 hours.c g

Adults Bacterial Ophthalmic Infections Polymyxin B and Neomycin Sulfates and Bacitracin Zinc Ophthalmic Ointment

Apply to the affected eye(s) every 3 or 4 hours for 7–10 days, depending on the severity of the infection.l

Polymyxin B and Neomycin Sulfates, Bacitracin Zinc, and Hydrocortisone Ophthalmic Ointment

Apply to the affected eye(s) every 3 or 4 hours, depending on the severity of the infection.d

Polymyxin B and Neomycin Sulfates and Dexamethasone Ophthalmic Ointment

Apply a 1.25-cm ribbon into the conjunctival sac of the affected eye(s) up to 3 or 4 times daily.i

Ophthalmic Suspension

Mild infections: 1 or 2 drops into the conjunctival sac of the affected eye(s) up to 4–6 times daily.j

Severe infections: 1 or 2 drops into the conjunctival sac of the affected eye(s) hourly.j Reduce dosing frequency as infection improves.j

Polymyxin B and Neomycin Sulfates and Gramicidin Ophthalmic Solution

1 or 2 drops into the affected eye(s) every 4 hours for 7–10 days.b

Severe infections: Up to 2 drops into the affected eye(s) every hour.b

Polymyxin B and Neomycin Sulfates and Hydrocortisone Ophthalmic Suspension

1 or 2 drops into the affected eye(s) every 3 or 4 hours, or more frequently as necessary.a

Polymyxin B and Neomycin Sulfates and Prednisolone Acetate Ophthalmic Suspension

1 or 2 drops into the affected eye(s) every 3–4 hours, or more frequently, as required.h For acute infection, may administer every 30 minutes.h Reduce dosing frequency as infection improves.h

To treat eyelids: 1 or 2 drops into the affected eye(s) every 3 or 4 hours.h (See Administration under Dosage and Administration.)

Polymyxin B Sulfate and Bacitracin Zinc Ophthalmic Ointment

Apply to affected eye(s) every 3 or 4 hours for 7–10 days, depending on the severity of the infection.k

Polymyxin B Sulfate and Trimethoprim Sulfate Ophthalmic Solution

1 drop into the affected eye(s) every 3 hours, up to 6 doses daily, for 7–10 days.e

Bacterial Otic Infections Polymyxin B and Neomycin Sulfates and Hydrocortisone Otic Solution or Suspension

4 drops into the affected ear(s) 3 or 4 times daily for up to 10 days.c g

Alternatively, insert a cotton wick that has been saturated with the otic preparation into the ear canal; keep the wick moist by adding additional drug every 4 hours.c g Replace the wick at least once every 24 hours.c g

Prescribing Limits Pediatric Patients Bacterial Ophthalmic Infections Polymyxin B Sulfate and Trimethoprim Sulfate: Ophthalmic Solution

Infants and children ?2 months of age: Maximum 6 doses in 24 hours.e

Bacterial Otic Infections Polymyxin B and Neomycin Sulfates and Hydrocortisone Otic Solution or Suspension

Children ?2 years of age: Maximum 10 consecutive days of therapy.c g

Adults Bacterial Ophthalmic Infections Polymyxin B Sulfate and Trimethoprim Sulfate Ophthalmic Solution

Maximum 6 doses in 24 hours.e

Bacterial Otic Infections Polymyxin B and Neomycin Sulfates and Hydrocortisone Otic Solution or Suspension

Maximum 10 consecutive days of therapy.c g

Special Populations

No special population dosage recommendations at this time.a b c d e g h i j k l

Cautions for Polymyxin B Sulfate Contraindications

Known hypersensitivity to polymyxin B or any ingredient in the formulation.a b c d e f g h i j k l

Warnings/Precautions Warnings Administration

Do not use otic preparations in any patient with a perforated tympanic membrane.c g

Ophthalmic Ointments

Ophthalmic ointments may delay corneal healing.f k l

Sensitivity Reactions Hypersensitivity Reactions

Hypersensitivity reactions possible (e.g., rash, itching, reddening, conjunctival and eyelid edema);b c d anaphylaxis reported rarely.a b d h If hypersensitivity occurs, discontinue the drug.a b c d g

Sulfite Sensitivity

Some formulations contain sulfites, which may cause allergic-type reactions (including anaphylaxis and life-threatening or less severe asthmatic episodes) in certain susceptible individuals.111 112 113 114 115 116 117 118 c

General Precautions Superinfection

Prolonged use may result in overgrowth of nonsusceptible organisms, including fungi.b c e f g h k If superinfection occurs, discontinue the drug and institute appropriate therapy.b e f g h

Use of Fixed Combinations

Concomitant topical corticosteroids may mask clinical signs of bacterial, fungal, or viral infections; prevent recognition of ineffectiveness of the antibiotic; or suppress hypersensitivity reactions to ingredients in the formulation.d h

When polymyxin B is used in fixed combination with other agents (corticosteroids, other anti-infectives), consider the cautions, precautions, and contraindications associated with the concomitant agent(s).a b c d e h l

Specific Populations Pregnancy

In fixed combination with other agents (corticosteroids, other anti-infectives): Category C.a b c d e g h l

Lactation

Ophthalmic preparations in fixed combination with other anti-infectives: Caution advised.b e h l

Ophthalmic preparations in fixed combination with other anti-infectives and hydrocortisone: Discontinue nursing or the drug.a d

Ophthalmic preparations in fixed combination with other anti-infectives and dexamethasone: Caution advised.i

Otic preparations in fixed combination with other anti-infectives and corticosteroids: Caution advised.c g

Pediatric Use

Safety and efficacy of trimethoprim sulfate and polymyxin B ophthalmic solution not established in infants <2 months of age.e

Safety and efficacy of neomycin and polymyxin B sulfates and hydrocortisone otic solution and suspension not established in children <2 years of age.c g

Safety and efficacy of other polymyxin B fixed-combination preparations (e.g., with corticosteroids and/or anti-infectives) not established.a b d h i j l

Geriatric Use

Ophthalmic preparations in fixed combination with other anti-infectives and hydrocortisone or prednisolone: No overall differences in safety or efficacy relative to younger patients.a d h

Neomycin and polymyxin B sulfates and dexamethasone ophthalmic ointment: No overall differences in safety or efficacy relative to younger patients.i

Otic preparations: Insufficient experience in patients ?65 years of age to determine whether geriatric patients respond differently than younger adults.c g

Common Adverse Effects

Local irritation.a b c d e g

Polymyxin B Sulfate Pharmacokinetics Absorption Bioavailability

Minimal or no absorption from intact or denuded skin or from mucous membranes.e f

Distribution Extent

Not known whether topical polymyxin B is distributed into human milk.b e (See Bioavailability under Pharmacokinetics.)

Stability Storage Ophthalmic Ointment

Polymyxin B and bacitracin zinc: 20–25°C.k

Polymyxin B and neomycin sulfates and bacitracin zinc: Tightly closed containers at 15–25°C.l

Polymyxin B and neomycin sulfates, bacitracin zinc, and hydrocortisone acetate: 15–25°C.d

Polymyxin B and neomycin sulfates and dexamethasone: 2–25°C.i

Solution

Polymyxin B and neomycin sulfates and gramicidin: Tightly closed containers at 15–25°C; protect from light.b

Polymyxin B sulfate and trimethoprim sulfate: 20–25°C; protect from light.e

Suspension

Polymyxin B sulfate and neomycin sulfates and dexamethasone: 8–27°C.j

Polymyxin B and neomycin sulfates and hydrocortisone: 20–25°C.a

Polymyxin B and neomycin sulfates and prednisolone acetate: Tightly closed containers at 15–25°C.h Store in upright position; protect from freezing.h

Otic Solution or Suspension

15–25°C.c g

Actions and SpectrumActions

Usually bactericidal.b e f l

Polymyxin B increases permeability of the bacterial cell wall membrane by interacting with the phospholipid components of the cell membrane.b e f l

Spectrum of activity of polymyxin B includes many aerobic gram-negative bacteria.e f k l Inactive against gram-positive bacteria and fungi.f

Gram-negative aerobes: Active against Enterobacter aerogenes, Escherichia coli, Haemophilus influenzae, Klebsiella pneumoniae, and Pseudomonas aeruginosa.e f

Neisseria and Proteus usually are resistant.f Complete cross-resistance between colistin derivatives and polymyxin B.f

Advice to Patients

Importance of discontinuing therapy and contacting clinician if condition worsens or does not improve or if signs of sensitivity (e.g., rash, itching, swelling, redness) occur.a b c d e g h l

Advise patients to immediately consult clinician regarding continued use of ophthalmic preparations if another eye condition (e.g., trauma, infection) occurs.f

Importance of not touching tip of container to the eye, eyelid, fingers, or any other surface to avoid contamination.a b c d e g h l Advise patient to keep container tightly closed when not in use.b h l

Importance of not wearing contact lenses if signs and symptoms of eye infection occur.h

Advise patient not to share the drug with any other person.a b d e h

Importance of patients informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs.a b c d e g

Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.a b c d e g h

Importance of informing patients of other important precautionary information.a b c d e g h (See Cautions.)

Preparations

Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.

Bacitracin Zinc and Polymyxin B Sulfate

Routes

Dosage Forms

Strengths

Brand Names

Manufacturer

Ophthalmic

Ointment

Bacitracin Zinc 500 units (of bacitracin) per g and Polymyxin B Sulfate 10,000 units (of polymyxin B) per g

AK-Poly-Bac

Akorn

Bacitracin Zinc and Polymyxin B Sulfate Ophthalmic Ointment

Bausch & Lomb, Fougera

Neomycin and Polymyxin B Sulfate and Bacitracin Zinc

Routes

Dosage Forms

Strengths

Brand Names

Manufacturer

Ophthalmic

Ointment

Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) per g, and Bacitracin Zinc 400 units (of bacitracin) per g

Neomycin and Polymyxin B Sulfates and Bacitracin Zinc Ophthalmic Ointment

Akorn, Fougera

Neosporin Ophthalmic Ointment

Monarch

* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name

Neomycin and Polymyxin B Sulfates, Bacitracin Zinc, and Hydrocortisone

Routes

Dosage Forms

Strengths

Brand Names

Manufacturer

Ophthalmic

Ointment

Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) per g, Bacitracin Zinc 400 units (of bacitracin) per g, and Hydrocortisone 1%*

Neomycin and Polymyxin B Sulfates, Bacitracin Zinc, and Hydrocortisone Ophthalmic Ointment

Bausch & Lomb, Fougera

Neomycin and Polymyxin B Sulfates, Bacitracin Zinc, and Hydrocortisone Acetate

Routes

Dosage Forms

Strengths

Brand Names

Manufacturer

Ophthalmic

Ointment

Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) per g, Bacitracin Zinc 400 units (of bacitracin) per g, and Hydrocortisone Acetate 1%

Neomycin and Polymyxin B Sulfates, Bacitracin Zinc, and Hydrocortisone Acetate Ophthalmic Ointment

Fougera

* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name

Neomycin and Polymyxin B Sulfates and Dexamethasone

Routes

Dosage Forms

Strengths

Brand Names

Manufacturer

Ophthalmic

Ointment

Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) per g, and Dexamethasone 0.1%*

Maxitrol (with parabens)

Alcon

Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Ointment

Bausch & Lomb, Falcon, Fougera

Suspension

Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) per mL, and Dexamethasone 0.1%*

Maxitrol (with benzalkonium chloride; viscous)

Alcon

Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension

Bausch & Lomb, Falcon

* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name

Neomycin and Polymyxin B Sulfates and Gramicidin

Routes

Dosage Forms

Strengths

Brand Names

Manufacturer

Ophthalmic

Solution

Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) per mL, and Gramicidin 0.0025%*

Neomycin and Polymyxin B Sulfates and Gramicidin Ophthalmic Solution

Bausch & Lomb

Neosporin Ophthalmic Solution (with alcohol 0.5%, propylene glycol, and thimerosal)

Monarch

* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name

Neomycin and Polymyxin B Sulfates and Hydrocortisone

Routes

Dosage Forms

Strengths

Brand Names

Manufacturer

Ophthalmic

Suspension

Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) per mL, and Hydrocortisone 1%

Neomycin and Polymyxin B Sulfates and Hydrocortisone Ophthalmic Suspension (with propylene glycol and thimerosal)

Falcon

Otic

Solution

Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) per mL, and Hydrocortisone 1%*

Cortisporin (with potassium metabisulfite and propylene glycol)

Monarch

Neomycin and Polymyxin B Sulfates and Hydrocortisone Otic Solution

Falcon

Suspension

Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) per mL, and Hydrocortisone 1%*

Neosporin and Polymyxin B Sulfates and Hydrocortisone Otic Suspension (with propylene glycol and thimerosal)

Falcon

Pediotic Suspension (with propylene glycol and thimerosal)

Monarch

Neomycin and Polymyxin B Sulfates and Prednisolone Acetate

Routes

Dosage Forms

Strengths

Brand Names

Manufacturer

Ophthalmic

Suspension

Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) per mL, and Prednisolone Acetate 0.5%

Poly-Pred (with propylene glycol and thimerosal; viscous)

Allergan

Polymyxin B Sulfate and Trimethoprim Sulfate

Routes

Dosage Forms

Strengths

Brand Names

Manufacturer

Ophthalmic

Solution

Polymyxin B Sulfate 10,000 units (of polymyxin B) per mL and Trimethoprim Sulfate 0.1% (of trimethoprim)

Polymyxin B Sulfate and Trimethoprim Sulfate Ophthalmic Solution (with benzalkonium chloride)

Akorn

Polymyxin B Sulfate and Trimethoprim Sulfate Ophthalmic Solution

Bausch & Lomb

Polytrim (with benzalkonium chloride)

Allergan

Disclaimer

This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.

The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.

AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions August 01, 2008. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.

References

Only references cited for selected revisions after 1984 are available electronically.

101. Monarch Pharmaceuticals, Inc. Cortisporin Ophthalmic Suspension Sterile (neomycin and polymyxin B sulfates and hydrocortisone ophthalmic suspension, USP) prescribing information. Bristol, TN; 2003 Jul.

102. Monarch. Neosporin Ophthalmic Solution Sterile (neomycin and polymyxin B sulfates and gramicidin ophthalmic solution, USP) prescribing information. Bristol, TN; 2003 Apr.

103. Monarch. Cortisporin Otic Solution Sterile (neomycin and polymyxin B sulfates and hydrocortisone otic solution, USP) prescribing information. Bristol, TN; 2003 Apr.

104. Bedford. Polymyxin B for injection 500,000 units prescribing information. Bedford, OH; 2004 Feb.

105. Akorn. Trimethoprim sulfate and polymyxin B sulfates ophthalmic solution prescribing information. Buffalo Grove, IL; 1998 Aug.

111. Food and Drug Administration. Sulfites in foods and drugs. FDA Drug Bull. 1983; 13:12. [PubMed 6604672]

112. Sogn D. The ubiquitous sulfites. JAMA. 1984; 251:2986 7. Editorial. [IDIS 185969] [PubMed 6716628]

113. Koepke JW, Christopher KL, Chai H et al. Dose dependent bronchospasm from sulfites in isoetharine. JAMA. 1984; 251:2982 3. [IDIS 185966] [PubMed 6716626]

114. Twarog FJ, Leung DYM. Anaphylaxis to a component of isoetharine (sodium bisulfite). JAMA. 1982; 248:2030 1. [IDIS 158261] [PubMed 7120631]

115. Baker GJ, Collett P, Allen DH. Bronchospasm induced by metabisulphite containing foods and drugs. Med J Aust. 1981; 2:614 7. [IDIS 146240] [PubMed 7334982]

116. Koepke JW, Selner JC, Dunhill AL. Presence of sulfur dioxide in commonly used bronchodilator solutions. J Allergy Clin Immunol. 1983; 72:504 8. [IDIS 178793] [PubMed 6630799]

117. Food and Drug Administration. Sulfiting agents; labeling in drugs for human use: warning statement. [Docket No. 84N 0113] Fed Regist. 1985; 50:47558 63.

118. Food and Drug Administration Center for Food Safety and Applied Nutrition. The reexamination of the GRAS status of sulfiting agents, January 1985. (Doc. No. 223-83-2020.) Bethesda, MD: FASEB Life Sciences Research Office.

a. Falcon Pharmaceuticals. Neomycin and polymyxin B sulfates, and hydrocortisone ophthalmic suspension prescribing information. Fort Worth, TX; 2006 Mar.

b. Monarch Pharmaceuticals, Inc. Neosporin (neomycin and polymyxin B sulfates and gramicidin ophthalmic solution, USP) prescribing information. Bristol, TN; 2003 Apr.

c. Monarch Pharmaceuticals, Inc. Cortisporin (neomycin and polymyxin B sulfates and hydrocortisone) otic solution prescribing information. Bristol, TN; 2003 Apr.

d. E. Fougera & Co. Neomycin and polymyxin B sulfates, and bacitracin zinc, with hydrocortisone acetate ophthalmic ointment prescribing information. Melville, NY; 2004 Aug.

e. Akorn, Inc. Trimethoprim sulfate and polymyxin B sulfate ophthalmic solution prescribing information. Buffalo Grove, IL; 2006 Mar.

f. AHFS drug information 2008. McEvoy GK, ed. Polymyxin B sulfate. Bethesda, MD: American Society of Health-System Pharmacists; 2008: 2853-5.

g. Monarch Pharmaceuticals, Inc. Pediotic (neomycin and polymyxin B sulfates and hydrocortisone otic suspension, USP) prescribing information. Bristol, TN; 2003 Apr.

h. Allergan, Inc. Poly-Pred (prednisolone acetate, neomycin sulfate, polymyxin B sulfate ophthalmic suspension, USP) prescribing information. Irvine, CA; 2004 Dec.

i. Alcon Laboratories, Inc. Maxitrol (neomycin and polymyxin b sulfates and dexamethasone ophthalmic ointment) prescribing information. Fort Worth, TX; 2003 Oct.

j. Alcon Laboratories, Inc. Maxitrol (neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension) prescribing information. Fort Worth, TX; 2003 Aug.

k. Akorn Pharmaceuticals, Inc. Bacitracin zinc and polymyxin B sulfate ophthalmic ointment, USP prescribing information. Buffalo Grove, IL. 2007 Aug.

l. E. Fougera & Co. Neomycin and polymyxin B sulfates, and bacitracin zinc ophthalmic ointment, USP prescribing information. Melville, NY; 2004 Jul.

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Vet One Chlorhexidine

Dosage Form: FOR ANIMAL USE ONLY
MWI/Vet One 2% Chlorhexidine solution MWI/Vet One 2% Chlorhexidine solution

ACTIVE INGREDIENTS:
2% Chlorhexidine Gluconate.

CAUTION:
Avoid contact with eyes and mucous membranes. This product is not to be used in ears. If contact is made, flush immediately and thoroughly with clean water. For use on horses and dogs.

Product No. 1CHL008
8CHL008-108
Distributed by:
MWI
Meridian, ID 83680
(888) 694-8381
MWI/Vet One 2% Chlorhexidine solution

PRODUCT DESCRIPION:
A topical aqueous cleaning solution for use on horses and dogs for application to superficial cuts, abrasions or insect stings.

DILUTE:
1 ounce (2 tablespoons) of Chlorhexidine Solution per gallon of clean water.
DIRECTIONS FOR USE:
Rinse skin area to be treated with Chlorhexidine Solution. Wipe away excess and pat dry with sterilized gauze or sponge.
MWI/Vet One 2% Chlorhexidine solution

Vet One Chlorhexidine 
chlorhexidine gluconate  solution Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 13985-017 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Chlorhexidine Gluconate (CHLORHEXIDINE) Chlorhexidine Gluconate 2 g  in 0.1 L Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 13985-017-80 3.785 L In 1 JUG None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/2010
Labeler - MWI VETERINARY SUPPLY CO (019926120) Revised: 01/2010MWI VETERINARY SUPPLY CO

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Mucositis Medications

Definition of Mucositis: Inflammation of a mucous membrane. Oral mucositis is a common complication of chemotherapy and radiation therapy.

Drugs associated with Mucositis

The following drugs and medications are in some way related to, or used in the treatment of Mucositis. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Drug List: Betasept-Liquid Biopatch Calgon-Vesta Caphosol-Solution Chlorostat Chlorostat-4 Denti-Care-Denti-Rinse Gelclair-Gel Hibiclens-Liquid Hibistat Kepivance Neutrasal-Powder Peridex-Solution Periochip Periogard-Solution Perisol-Oral-Rinse Salivart-Spray Scrub-Care Spectrum-4

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Caphosol Solution

Generic Name: Artificial Saliva
Brand Name: Caphosol
Caphosol Solution is used for:

Relieving dry mouth and throat.

Caphosol Solution is an artificial saliva. It works by moistening and lubricating the mouth and throat.

Do NOT use Caphosol Solution if: you are allergic to any ingredient in Caphosol Solution

Contact your doctor or health care provider right away if any of these apply to you.

Before using Caphosol Solution:

Some medical conditions may interact with Caphosol Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances

Some MEDICINES MAY INTERACT with Caphosol Solution. However, no specific interactions with Caphosol Solution are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Caphosol Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Caphosol Solution:

Use Caphosol Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Mix 1 blue ( Caphosol A) and 1 clear ampule ( Caphosol B) in a clean glass. Swish half of the solution thoroughly in your mouth for 1 minute, then spit out. Repeat with the remaining half of the solution, then spit out. Use immediately after mixing the ampules. Do not eat or drink for at least 15 minutes after use. Do not use if the seal of the container is broken or the container shows signs of leakage or damage. If you miss taking a dose of Caphosol Solution for 1 or more days, there is no cause for concern. If your doctor recommended that you take it, try to remember your dose every day.

Ask your health care provider any questions you may have about how to use Caphosol Solution.

Important safety information: PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Caphosol Solution, discuss with your doctor the benefits and risks of using Caphosol Solution during pregnancy. It is unknown if Caphosol Solution is excreted in breast milk. If you are or will be breast-feeding while you are using Caphosol Solution, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Caphosol Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. When used in small doses, no COMMON side effects have been reported with this product. Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Caphosol side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.

Proper storage of Caphosol Solution:

Store Caphosol Solution at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Do not refrigerate. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Caphosol Solution out of the reach of children and away from pets.

General information: If you have any questions about Caphosol Solution, please talk with your doctor, pharmacist, or other health care provider. Caphosol Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Caphosol Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Caphosol resources Caphosol Side Effects (in more detail) Caphosol Use in Pregnancy & Breastfeeding Caphosol Support Group 0 Reviews for Caphosol - Add your own review/rating Compare Caphosol with other medications Mucositis Xerostomia

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Artificial Saliva Solution

Generic Name: Artificial Saliva
Brand Name: Caphosol
Artificial Saliva Solution is used for:

Relieving dry mouth and throat.

Artificial Saliva Solution is an artificial saliva. It works by moistening and lubricating the mouth and throat.

Do NOT use Artificial Saliva Solution if: you are allergic to any ingredient in Artificial Saliva Solution

Contact your doctor or health care provider right away if any of these apply to you.

Before using Artificial Saliva Solution:

Some medical conditions may interact with Artificial Saliva Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances

Some MEDICINES MAY INTERACT with Artificial Saliva Solution. However, no specific interactions with Artificial Saliva Solution are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Artificial Saliva Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Artificial Saliva Solution:

Use Artificial Saliva Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Mix 1 blue ( Caphosol A) and 1 clear ampule ( Caphosol B) in a clean glass. Swish half of the solution thoroughly in your mouth for 1 minute, then spit out. Repeat with the remaining half of the solution, then spit out. Use immediately after mixing the ampules. Do not eat or drink for at least 15 minutes after use. Do not use if the seal of the container is broken or the container shows signs of leakage or damage. If you miss taking a dose of Artificial Saliva Solution for 1 or more days, there is no cause for concern. If your doctor recommended that you take it, try to remember your dose every day.

Ask your health care provider any questions you may have about how to use Artificial Saliva Solution.

Important safety information: PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Artificial Saliva Solution, discuss with your doctor the benefits and risks of using Artificial Saliva Solution during pregnancy. It is unknown if Artificial Saliva Solution is excreted in breast milk. If you are or will be breast-feeding while you are using Artificial Saliva Solution, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Artificial Saliva Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. When used in small doses, no COMMON side effects have been reported with this product. Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.

Proper storage of Artificial Saliva Solution:

Store Artificial Saliva Solution at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Do not refrigerate. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Artificial Saliva Solution out of the reach of children and away from pets.

General information: If you have any questions about Artificial Saliva Solution, please talk with your doctor, pharmacist, or other health care provider. Artificial Saliva Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Artificial Saliva Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Artificial Saliva resources Artificial Saliva Use in Pregnancy & Breastfeeding Artificial Saliva Support Group 2 Reviews for Artificial Saliva - Add your own review/rating Compare Artificial Saliva with other medications Mucositis Xerostomia

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Lugols Strong Iodine Solution

Dosage Form: solution
Lugols Strong Iodine Solution CONTENTS      

Iodine 0.05 g/ml, Potassium Iodide 0.105 g/ml.

DESCRIPTION      

LUGOL’S is an aqueous solution containing Iodine 5%, and potassium iodide 10%, w/v (LUGOL’s Solution). LUGOL’s is a transparent liquid with a deep brown color and the odor of iodine.

HOW SUPPLIED      

LUGOL’S is supplied in 8 ml glass single-use bottles.

INDICATIONS AND USAGE      

LUGOL’s is a topical antiseptic. Strong Iodine Solution is a germicide and fungicide. LUGOL’s is preservative-free.

ADMINISTRATION      

LUGOL’S is applied directly to areas needing antiseptic.

WARNINGS      

For External Use Only.

CONTRAINDICATIONS      

Iodide preparations are contraindicated in patients with known sensitivity to the drugs.

CAUTION      

Federal law restricts this device to sale by or on the order of a physician.

STORAGE      

Keep tightly closed. Protect from light.  DO NOT use if seal has been broken. Store at controlled room temperature 15°-30°C (59°-86°F).

DISPOSAL      

Opened containers with unused portions of product and applicator swabs containing residual product should be placed in a suitable, dry container for disposal following local hazardous waste practices. Waste containing LUGOL’S should not be subjected to any thermal process whether intended for destruction or recycling purposes.

PRINCIPAL DISPLAY PANEL

Lugol’s

Strong Iodine Solution USP

Contents      

One Dozen (12)

8ml Vials

LUGOLS STRONG IODINE 
iodine potassium iodide  solution Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 59365-6064 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (IODINE) IODINE 0.05 g  in 1 mL POTASSIUM IODIDE (POTASSIUM CATION) POTASSIUM IODIDE 0.105 g  in 1 mL Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 59365-6064-1 12 VIAL In 1 CARTON contains a VIAL, SINGLE-USE 1 8 mL In 1 VIAL, SINGLE-USE This package is contained within the CARTON (59365-6064-1)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 10/01/1992
Labeler - CooperSurgical, Inc. (801895244) Revised: 11/2009CooperSurgical, Inc.
More Lugols Strong Iodine Solution resources Lugols Strong Iodine Solution Drug Interactions Lugols Strong Iodine Solution Support Group 0 Reviews · Be the first to review/rate this drug

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Formaldehyde Solution

Pronunciation: for-MAL-de-hyde
Generic Name: Formaldehyde
Brand Name: Examples include Formadon and Lazerformalyde
Formaldehyde Solution is used for:

Drying skin before or after surgical removal of warts or where dryness is required. It may also be used for treating excessive foot moisture or for other conditions as determined by your doctor.

Formaldehyde Solution is a drying agent. It works by drying excessive moisture.

Do NOT use Formaldehyde Solution if: you are allergic to any ingredient in Formaldehyde Solution

Contact your doctor or health care provider right away if any of these apply to you.

Before using Formaldehyde Solution:

Some medical conditions may interact with Formaldehyde Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances

Some MEDICINES MAY INTERACT with Formaldehyde Solution. However, no specific interactions with Formaldehyde Solution are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Formaldehyde Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Formaldehyde Solution:

Use Formaldehyde Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Apply with roll-on applicator to affected areas. Do not shake bottle with the cap removed. Do not bandage or wrap the affected area unless directed otherwise by your doctor. Wash your hands immediately after using Formaldehyde Solution, unless your hands are part of the treated area. If you miss a dose of Formaldehyde Solution, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Formaldehyde Solution.

Important safety information: Skin should be checked for sensitivity to formaldehyde prior to application because it may be irritating and sensitizing to the skin of some patients. Avoid getting Formaldehyde Solution in your eyes, nose, or mouth, or on your face. PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Formaldehyde Solution, discuss with your doctor the benefits and risks of using Formaldehyde Solution during pregnancy. It is unknown if Formaldehyde Solution is excreted in breast milk. If you are or will be breast-feeding while you are using Formaldehyde Solution, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Formaldehyde Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Skin redness or irritation.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); persisting irritation or redness.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Formaldehyde side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.

Proper storage of Formaldehyde Solution:

Store Formaldehyde Solution at room temperature, between 59 and 86 degrees F (15 and 30 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Keep Formaldehyde Solution out of the reach of children and away from pets.

General information: If you have any questions about Formaldehyde Solution, please talk with your doctor, pharmacist, or other health care provider. Formaldehyde Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Formaldehyde Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Formaldehyde resources Formaldehyde Side Effects (in more detail) Formaldehyde Use in Pregnancy & Breastfeeding Formaldehyde Support Group 0 Reviews · Be the first to review/rate this drug

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Lazerformalyde Solution

Pronunciation: for-MAL-de-hyde
Generic Name: Formaldehyde
Brand Name: Examples include Formadon and Lazerformalyde
Lazerformalyde Solution is used for:

Drying skin before or after surgical removal of warts or where dryness is required. It may also be used for treating excessive foot moisture or for other conditions as determined by your doctor.

Lazerformalyde Solution is a drying agent. It works by drying excessive moisture.

Do NOT use Lazerformalyde Solution if: you are allergic to any ingredient in Lazerformalyde Solution

Contact your doctor or health care provider right away if any of these apply to you.

Before using Lazerformalyde Solution:

Some medical conditions may interact with Lazerformalyde Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances

Some MEDICINES MAY INTERACT with Lazerformalyde Solution. However, no specific interactions with Lazerformalyde Solution are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Lazerformalyde Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Lazerformalyde Solution:

Use Lazerformalyde Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Apply with roll-on applicator to affected areas. Do not shake bottle with the cap removed. Do not bandage or wrap the affected area unless directed otherwise by your doctor. Wash your hands immediately after using Lazerformalyde Solution, unless your hands are part of the treated area. If you miss a dose of Lazerformalyde Solution, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Lazerformalyde Solution.

Important safety information: Skin should be checked for sensitivity to formaldehyde prior to application because it may be irritating and sensitizing to the skin of some patients. Avoid getting Lazerformalyde Solution in your eyes, nose, or mouth, or on your face. PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Lazerformalyde Solution, discuss with your doctor the benefits and risks of using Lazerformalyde Solution during pregnancy. It is unknown if Lazerformalyde Solution is excreted in breast milk. If you are or will be breast-feeding while you are using Lazerformalyde Solution, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Lazerformalyde Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Skin redness or irritation.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); persisting irritation or redness.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Lazerformalyde side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.

Proper storage of Lazerformalyde Solution:

Store Lazerformalyde Solution at room temperature, between 59 and 86 degrees F (15 and 30 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Keep Lazerformalyde Solution out of the reach of children and away from pets.

General information: If you have any questions about Lazerformalyde Solution, please talk with your doctor, pharmacist, or other health care provider. Lazerformalyde Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Lazerformalyde Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Lazerformalyde resources Lazerformalyde Side Effects (in more detail) Lazerformalyde Use in Pregnancy & Breastfeeding Lazerformalyde Support Group 0 Reviews · Be the first to review/rate this drug

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Povidone/Iodine Solution

Pronunciation: POE-vi-done/EYE-oh-dine
Generic Name: Povidone/Iodine
Brand Name: Examples include Minidyne and Polydine
Povidone/Iodine Solution is used for:

Treating minor wounds and infections, as well as killing bacteria.

Povidone/Iodine Solution is an antiseptic combination. It works by killing sensitive bacteria.

Do NOT use Povidone/Iodine Solution if: you are allergic to any ingredient in Povidone/Iodine Solution

Contact your doctor or health care provider right away if any of these apply to you.

Before using Povidone/Iodine Solution:

Some medical conditions may interact with Povidone/Iodine Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have serious burns or deep puncture wounds

Some MEDICINES MAY INTERACT with Povidone/Iodine Solution. However, no specific interactions are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Povidone/Iodine Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Povidone/Iodine Solution:

Use Povidone/Iodine Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Clean the affected area. Apply a small amount of Povidone/Iodine Solution to the affected area. The area may be left uncovered, or you may cover it with a sterile bandage. If you miss a dose of Povidone/Iodine Solution, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Povidone/Iodine Solution.

Important safety information: If you have had a severe allergic reaction to Povidone/Iodine Solution or a medicine that contains iodine, contact your doctor or pharmacist immediately. A severe allergic reaction includes a severe rash, hives, difficulty breathing, or dizziness. If you have questions about whether you are allergic to Povidone/Iodine Solution or if a certain medicine contains iodine, contact your doctor or pharmacist. If you experience a skin rash, hives, or itching, or any other unusual reaction after using this product, discontinue use and contact your doctor as soon as possible. Povidone/Iodine Solution is for external use only. Do not get Povidone/Iodine Solution in your eyes, nose, or mouth. Do not use Povidone/Iodine Solution over large areas of the body or for more than 1 week unless advised to do so by your doctor. Contact your doctor before using Povidone/Iodine Solution on serious burns, deep wounds, or puncture wounds. PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Povidone/Iodine Solution, discuss with your doctor the benefits and risks of using Povidone/Iodine Solution during pregnancy. It is unknown if Povidone/Iodine Solution is excreted in breast milk. If you are or will be breast-feeding while you are using Povidone/Iodine Solution, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Povidone/Iodine Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Skin irritation.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.

Proper storage of Povidone/Iodine Solution:

Store Povidone/Iodine Solution at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Povidone/Iodine Solution out of the reach of children and away from pets.

General information: If you have any questions about Povidone/Iodine Solution, please talk with your doctor, pharmacist, or other health care provider. Povidone/Iodine Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Povidone/Iodine Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Povidone/Iodine resources Povidone/Iodine Use in Pregnancy & Breastfeeding Povidone/Iodine Support Group 0 Reviews · Be the first to review/rate this drug

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Synvisc Solution

Pronunciation: HIGH-lan
Generic Name: Hylan
Brand Name: Synvisc
Synvisc Solution is used for:

Treating pain associated with osteoarthritis of the knee.

Synvisc Solution is a visco supplement. It works by replacing the viscous or "thick" fluid naturally found in joints. The viscous fluid is needed to coat and protect the cartilage and joint of the knee, which lessens the pain of osteoarthritis.

Do NOT use Synvisc Solution if: you are allergic to any ingredient in Synvisc Solution you have an infection where Synvisc Solution will be injected

Contact your doctor or health care provider right away if any of these apply to you.

Before using Synvisc Solution:

Some medical conditions may interact with Synvisc Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have a skin disease if you have an allergy to bird proteins, feathers, or eggs if you have blood flow problems

Some MEDICINES MAY INTERACT with Synvisc Solution. However, no specific interactions with Synvisc Solution are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Synvisc Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Synvisc Solution:

Use Synvisc Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Synvisc Solution comes with an additional patient leaflet. Read it carefully and reread it each time you get Synvisc Solution refilled. Synvisc Solution is administered as an injection at your doctor's office, hospital, or clinic. Do not miss your doctor appointments while you are taking Synvisc Solution. If you must miss an appointment, notify your doctor as soon as possible. Do not miss your doctor appointments while you are taking Synvisc Solution. If you must miss an appointment, notify your doctor as soon as possible. If you miss a dose of Synvisc Solution, contact your doctor right away.

Ask your health care provider any questions you may have about how to use Synvisc Solution.

Important safety information: It may take several injections for Synvisc Solution to work fully. Complete the full treatment course, even if you are already feeling better. Avoid strenuous activities or prolonged weight-bearing activities, such as jogging or tennis, after receiving an injection. Use Synvisc Solution with extreme caution in CHILDREN. Safety and effectiveness have not been confirmed. PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Synvisc Solution during pregnancy. It is unknown if Synvisc Solution is excreted in breast milk. If you are or will be breast-feeding while you are using Synvisc Solution, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Synvisc Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Knee pain or swelling after injection.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); ankle swelling; bruising; calf cramping; fast heartbeat; fever; hemorrhoids; muscle pain; nausea; persistent pain, redness, or swelling at injection site; sweating.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Synvisc side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.

Proper storage of Synvisc Solution:

Synvisc Solution is usually handled and stored by a health care provider. Keep Synvisc Solution, as well as needles and syringes, out of the reach of children and away from pets.

General information: If you have any questions about Synvisc Solution, please talk with your doctor, pharmacist, or other health care provider. Synvisc Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Synvisc Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Synvisc resources Synvisc Side Effects (in more detail) Synvisc Use in Pregnancy & Breastfeeding Synvisc Drug Interactions Synvisc Support Group 6 Reviews for Synvisc - Add your own review/rating Compare Synvisc with other medications Osteoarthritis

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Sorbitol Solution

Pronunciation: SOR-bi-tole
Generic Name: Sorbitol
Brand Name: Generic only. No brands available.
Sorbitol Solution is used for:

Treating occasional constipation. It may also be used for other conditions as determined by your doctor.

Sorbitol Solution is a hyperosmotic laxative. It works by retaining fluid in the colon, which helps to increase muscle movement in the intestines.

Do NOT use Sorbitol Solution if: you are allergic to any ingredient in Sorbitol Solution

Contact your doctor or health care provider right away if any of these apply to you.

Before using Sorbitol Solution:

Some medical conditions may interact with Sorbitol Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have an acid-base imbalance or diabetes if you have abdominal pain, nausea, vomiting, or rectal bleeding

Some MEDICINES MAY INTERACT with Sorbitol Solution. However, no specific interactions with Sorbitol Solution are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Sorbitol Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Sorbitol Solution:

Use Sorbitol Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Sorbitol Solution may be taken with or without food. Use a measuring device marked for medicine dosing. Ask your pharmacist for help if you are unsure of how to measure your dose. Do not take additional laxatives or stool softeners while taking Sorbitol Solution unless directed by your doctor. If you are using Sorbitol Solution as a rectal enema, follow the directions given with the enema. Ask your doctor or pharmacist any questions you may have about giving an enema. Do not exceed the recommended dose or use Sorbitol Solution for longer than 1 week without checking with your doctor. If you miss a dose of Sorbitol Solution, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Sorbitol Solution.

Important safety information: If you have rectal bleeding or failure to have a bowel movement after use, contact your doctor immediately. If you notice a sudden change in bowel habits that lasts for 2 weeks or more, consult your doctor. PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Sorbitol Solution, discuss with your doctor the benefits and risks of using Sorbitol Solution during pregnancy. If you are or will be breast-feeding while you are using Sorbitol Solution, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Sorbitol Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Anal irritation; diarrhea; gas; nausea; stomach cramps.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); continuing constipation; dizziness; rectal bleeding; sudden weight gain; unusual swelling; vomiting; weakness.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.

Proper storage of Sorbitol Solution:

Store Sorbitol Solution at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Do not freeze. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Sorbitol Solution out of the reach of children and away from pets.

General information: If you have any questions about Sorbitol Solution, please talk with your doctor, pharmacist, or other health care provider. Sorbitol Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Sorbitol Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Sorbitol resources Sorbitol Use in Pregnancy & Breastfeeding Sorbitol Drug Interactions Sorbitol Support Group 0 Reviews for Sorbitol - Add your own review/rating Compare Sorbitol with other medications Constipation

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Pedialyte Singles Solution

Pronunciation: e-LECK-troe-lite
Generic Name: Electrolyte
Brand Name: Pedialyte Singles
Pedialyte Singles Solution is used for:

Treating or preventing dehydration caused by vomiting or diarrhea. It may also be used for other conditions as determined by your doctor.

Pedialyte Singles Solution is a carbohydrate and electrolyte combination. It works by replacing electrolytes and carbohydrates in the body to prevent dehydration.

Do NOT use Pedialyte Singles Solution if: you are allergic to any ingredient in Pedialyte Singles Solution you have high blood potassium levels

Contact your doctor or health care provider right away if any of these apply to you.

Before using Pedialyte Singles Solution:

Some medical conditions may interact with Pedialyte Singles Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have heart failure, fluid retention (eg, swelling of the hands, ankles, or feet), intestinal holes or punctures, difficulty urinating, kidney problems, or unexplained rectal bleeding if you have severe or persistent vomiting, severe diarrhea, or if you are dehydrated if you are unable to properly absorb glucose from food

Some MEDICINES MAY INTERACT with Pedialyte Singles Solution. However, no specific interactions with Pedialyte Singles Solution are known at this time.

Ask your health care provider if Pedialyte Singles Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Pedialyte Singles Solution:

Use Pedialyte Singles Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Take Pedialyte Singles Solution by mouth with or without food. Do not mix Pedialyte Singles Solution with water or any other liquid. Do not heat Pedialyte Singles Solution. Each container of Pedialyte Singles Solution is intended for a single use. Discard the container and any unused portion of medicine immediately after the first use. Do not reuse the container. If you miss a dose of Pedialyte Singles Solution, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Pedialyte Singles Solution.

Important safety information: If vomiting, fever, stomach pain or bloating, or diarrhea that lasts longer than 24 hours occurs, check with your doctor. Some of these products contain phenylalanine. If you must have a diet that is low in phenylalanine, ask your pharmacist if it is in your product. Do not use Pedialyte Singles Solution in CHILDREN younger than 1 year old without first checking with your doctor. PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Pedialyte Singles Solution while you are pregnant. It is not known if Pedialyte Singles Solution is found in breast milk. If you are or will be breast-feeding while you use Pedialyte Singles Solution, check with your doctor. Discuss any possible risks to your baby. Possible side effects of Pedialyte Singles Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. When used in small doses, no COMMON side effects have been reported with this product. Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Pedialyte Singles side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.

Proper storage of Pedialyte Singles Solution:

Store Pedialyte Singles Solution at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Pedialyte Singles Solution out of the reach of children and away from pets.

General information: If you have any questions about Pedialyte Singles Solution, please talk with your doctor, pharmacist, or other health care provider. Pedialyte Singles Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Pedialyte Singles Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Pedialyte Singles resources Pedialyte Singles Side Effects (in more detail) Pedialyte Singles Support Group 0 Reviews · Be the first to review/rate this drug

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Carnitor SF Solution

Pronunciation: LEE-voe-KAR-ni-teen
Generic Name: Levocarnitine
Brand Name: Examples include Carnitor and Carnitor SF
Carnitor SF Solution is used for:

Treating low levels of levocarnitine in the body and treating patients with metabolism problems that may cause low levels of levocarnitine. It may also be used for other conditions as determined by your doctor.

Carnitor SF Solution is an amino acid derivative. It works by replacing levocarnitine in the body when your body does not produce enough.

Do NOT use Carnitor SF Solution if: you are allergic to any ingredient in Carnitor SF Solution

Contact your doctor or health care provider right away if any of these apply to you.

Before using Carnitor SF Solution:

Some medical conditions may interact with Carnitor SF Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have kidney problems or seizures

Some MEDICINES MAY INTERACT with Carnitor SF Solution. However, no specific interactions with Carnitor SF Solution are known at this time.

Ask your health care provider if Carnitor SF Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Carnitor SF Solution:

Use Carnitor SF Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Take Carnitor SF Solution by mouth during or after meals unless otherwise directed by your doctor. Carnitor SF Solution may be poured into drinks or liquid foods to help prevent taste changes. Finish all of the liquid. Use a measuring device marked for medicine dosing. Ask your pharmacist for help if you are unsure how to measure your dose. Take each dose of Carnitor SF Solution slowly and space your doses evenly throughout the day. If you miss a dose of Carnitor SF Solution, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Carnitor SF Solution.

Important safety information: Do not use products containing D,L-carnitine (vitamin BT), which are available without a prescription and in health food stores, without first checking with your doctor. Lab tests, including blood chemistry and blood carnitine levels, may be performed while you use Carnitor SF Solution. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments. PREGNANCY and BREAST-FEEDING: If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Carnitor SF Solution while you are pregnant. It is not known whether Carnitor SF Solution is found in breast milk. If you are or will be breast-feeding while you use Carnitor SF Solution, check with your doctor. Discuss any possible risks to your baby. Possible side effects of Carnitor SF Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Bad taste in mouth; diarrhea; mild muscle weakness; nausea; stomach cramps; unpleasant body odor; vomiting.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); seizures.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Carnitor SF side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include severe diarrhea.

Proper storage of Carnitor SF Solution:

Store Carnitor SF Solution at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not freeze. Do not store in the bathroom. Keep Carnitor SF Solution out of the reach of children and away from pets.

General information: If you have any questions about Carnitor SF Solution, please talk with your doctor, pharmacist, or other health care provider. Carnitor SF Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Carnitor SF Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Carnitor SF resources Carnitor SF Side Effects (in more detail) Carnitor SF Use in Pregnancy & Breastfeeding Carnitor SF Support Group 0 Reviews for Carnitor SF - Add your own review/rating Compare Carnitor SF with other medications Carnitine Deficiency Peripheral Neuropathy

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Ascorbic Acid Solution

Pronunciation: ASS-kor-bik ASS-id
Generic Name: Ascorbic Acid
Brand Name: Cecon and Protexin
Ascorbic Acid Solution is used for:

Treating and preventing low levels of vitamin C. It may also be used for other conditions as determined by your doctor.

Ascorbic Acid Solution is a vitamin. It works by supplementing vitamin C, which is used in many functions in the body.

Do NOT use Ascorbic Acid Solution if: you are allergic to any ingredient in Ascorbic Acid Solution

Contact your doctor or health care provider right away if any of these apply to you.

Before using Ascorbic Acid Solution:

Some medical conditions may interact with Ascorbic Acid Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have diabetes, glucose-6-phosphate dehydrogenase deficiency, a high iron level in the blood, anemia (eg, sickle cell, sideroblastic, thalassemia), or kidney stones

Some MEDICINES MAY INTERACT with Ascorbic Acid Solution. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin) because side effects may be increased by Ascorbic Acid Solution

This may not be a complete list of all interactions that may occur. Ask your health care provider if Ascorbic Acid Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Ascorbic Acid Solution:

Use Ascorbic Acid Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ascorbic Acid Solution may be taken with or without food. You may drop the dose of Ascorbic Acid Solution directly into your mouth or mix it with cereal, milk, or water. Take Ascorbic Acid Solution with a full glass of water (8 oz/240 mL). Do not lie down for 30 minutes after taking Ascorbic Acid Solution. Use a measuring device marked for medicine dosing. Ask your pharmacist for help if you are unsure of how to measure your dose. If you miss a dose of Ascorbic Acid Solution, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Ascorbic Acid Solution.

Important safety information: Do not take large doses of vitamins (megadoses or megavitamin therapy) while taking Ascorbic Acid Solution unless directed to by your doctor. Ascorbic Acid Solution may cause incorrect results with some in-home cholesterol test kits. Check with your doctor or pharmacist if you are taking Ascorbic Acid Solution and need to check your cholesterol at home. Diabetes patients - Ascorbic Acid Solution may cause incorrect test results with some urine glucose tests. Check with your doctor before you adjust the dose of your diabetes medicine or change your diet. Ascorbic Acid Solution may cause incorrect test results with kits used to check for blood in the stool. Check with your doctor if you are taking Ascorbic Acid Solution when using the test kit. PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Ascorbic Acid Solution, discuss with your doctor the benefits and risks of using Ascorbic Acid Solution during pregnancy. Ascorbic Acid Solution is excreted in breast milk. If you are or will be breast-feeding while you are using Ascorbic Acid Solution, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Ascorbic Acid Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Diarrhea; nausea; upset stomach; vomiting.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); kidney stones (eg, abdominal pain/back pain, painful urination).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Ascorbic Acid side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include gout.

Proper storage of Ascorbic Acid Solution:

Store Ascorbic Acid Solution at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Ascorbic Acid Solution out of the reach of children and away from pets.

General information: If you have any questions about Ascorbic Acid Solution, please talk with your doctor, pharmacist, or other health care provider. Ascorbic Acid Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Ascorbic Acid Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Ascorbic Acid resources Ascorbic Acid Side Effects (in more detail) Ascorbic Acid Use in Pregnancy & Breastfeeding Ascorbic Acid Drug Interactions Ascorbic Acid Support Group 0 Reviews for Ascorbic Acid - Add your own review/rating Compare Ascorbic Acid with other medications Dietary Supplementation Scurvy Urinary Acidification

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Cromolyn Solution

Pronunciation: KROE-moe-lin
Generic Name: Cromolyn
Brand Name: Examples include Nasal Allergy Control and NasalCrom
Cromolyn Solution is used for:

Preventing and relieving symptoms of hay fever and allergies, including runny/itchy nose, sneezing, and nasal congestion. It may be used alone or with other allergy medications.

Cromolyn Solution is a mast cell stabilizer. It works by stabilizing mast cells and preventing them from releasing their irritating chemicals.

Do NOT use Cromolyn Solution if: you are allergic to any ingredient in Cromolyn Solution

Contact your doctor or health care provider right away if any of these apply to you.

Before using Cromolyn Solution:

Some medical conditions may interact with Cromolyn Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have liver or kidney problems

Some MEDICINES MAY INTERACT with Cromolyn Solution. However, no specific interactions with Cromolyn Solution are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Cromolyn Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Cromolyn Solution:

Use Cromolyn Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Blow your nose before using Cromolyn Solution. Hold the pump with your thumb at the bottom and the nozzle between your fingers. If this is your first time using the pump, or if you have not used the pump for several days, spray into the air until you see a fine mist. Insert the nozzle into your nostril and spray upward one time while breathing in through the nose. Repeat in the other nostril. To keep the pump clean, wipe the nozzle and replace the cap and safety clip provided. For best results, start using Cromolyn Solution 1 week before contact with the cause of your allergies. If you miss a dose of Cromolyn Solution, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Cromolyn Solution.

Important safety information: Cromolyn Solution may cause drowsiness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Cromolyn Solution Several days to a few weeks may pass before you feel the full benefit of Cromolyn Solution. Cromolyn Solution is not recommended for use in CHILDREN younger than 2 years of age. Safety and effectiveness in this age group have not been confirmed. PREGNANCY and BREAST-FEEDING: If you are pregnant or plan on becoming pregnant, discuss with your doctor the benefits and risks of using Cromolyn Solution during pregnancy. It is unknown if Cromolyn Solution is excreted in breast milk. If you are or will be breast-feeding, check with your doctor to discuss the benefits and risks to your baby. Possible side effects of Cromolyn Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Bad taste in the mouth; drowsiness; headache; irritated or burning sensation in the nose; sneezing.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Cromolyn Solution may be harmful if swallowed.

Proper storage of Cromolyn Solution:

Store Cromolyn Solution at room temperature between 68 and 77 degrees F (20 and 25 degrees C), away from heat, moisture, and light. Do not store in the bathroom. Keep Cromolyn Solution out of the reach of children and away from pets.

General information: If you have any questions about Cromolyn Solution, please talk with your doctor, pharmacist, or other health care provider. Cromolyn Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Cromolyn Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Cromolyn resources Cromolyn Use in Pregnancy & BreastfeedingCromolyn Support Group0 Reviews for Cromolyn - Add your own review/rating Compare Cromolyn with other medications Hay Fever

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Shunt Infection Medications

Drugs associated with Shunt Infection

The following drugs and medications are in some way related to, or used in the treatment of Shunt Infection. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Drug List: Lyphocin Nebcin Tobi-Solution Vancocin Vancocin-Hcl Vancocin-Hcl-Pulvules

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McCune-Albright Syndrome Medications

Definition of McCune-Albright Syndrome: A genetic disease affecting the bones and pigmentation of the skin, and causing hormonal problems featuring premature sexual development.

Drugs associated with McCune-Albright Syndrome

The following drugs and medications are in some way related to, or used in the treatment of McCune-Albright Syndrome. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Learn more about McCune-Albright Syndrome

Medical Encyclopedia:

McCune-Albright syndrome
Drug List: Arimidex Nolvadex Soltamox-Solution

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NasalCrom Solution

Pronunciation: KROE-moe-lin
Generic Name: Cromolyn
Brand Name: Examples include Nasal Allergy Control and NasalCrom
NasalCrom Solution is used for:

Preventing and relieving symptoms of hay fever and allergies, including runny/itchy nose, sneezing, and nasal congestion. It may be used alone or with other allergy medications.

NasalCrom Solution is a mast cell stabilizer. It works by stabilizing mast cells and preventing them from releasing their irritating chemicals.

Do NOT use NasalCrom Solution if: you are allergic to any ingredient in NasalCrom Solution

Contact your doctor or health care provider right away if any of these apply to you.

Before using NasalCrom Solution:

Some medical conditions may interact with NasalCrom Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have liver or kidney problems

Some MEDICINES MAY INTERACT with NasalCrom Solution. However, no specific interactions with NasalCrom Solution are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if NasalCrom Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use NasalCrom Solution:

Use NasalCrom Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Blow your nose before using NasalCrom Solution. Hold the pump with your thumb at the bottom and the nozzle between your fingers. If this is your first time using the pump, or if you have not used the pump for several days, spray into the air until you see a fine mist. Insert the nozzle into your nostril and spray upward one time while breathing in through the nose. Repeat in the other nostril. To keep the pump clean, wipe the nozzle and replace the cap and safety clip provided. For best results, start using NasalCrom Solution 1 week before contact with the cause of your allergies. If you miss a dose of NasalCrom Solution, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use NasalCrom Solution.

Important safety information: NasalCrom Solution may cause drowsiness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to NasalCrom Solution Several days to a few weeks may pass before you feel the full benefit of NasalCrom Solution. NasalCrom Solution is not recommended for use in CHILDREN younger than 2 years of age. Safety and effectiveness in this age group have not been confirmed. PREGNANCY and BREAST-FEEDING: If you are pregnant or plan on becoming pregnant, discuss with your doctor the benefits and risks of using NasalCrom Solution during pregnancy. It is unknown if NasalCrom Solution is excreted in breast milk. If you are or will be breast-feeding, check with your doctor to discuss the benefits and risks to your baby. Possible side effects of NasalCrom Solution:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Bad taste in the mouth; drowsiness; headache; irritated or burning sensation in the nose; sneezing.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: NasalCrom side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. NasalCrom Solution may be harmful if swallowed.

Proper storage of NasalCrom Solution:

Store NasalCrom Solution at room temperature between 68 and 77 degrees F (20 and 25 degrees C), away from heat, moisture, and light. Do not store in the bathroom. Keep NasalCrom Solution out of the reach of children and away from pets.

General information: If you have any questions about NasalCrom Solution, please talk with your doctor, pharmacist, or other health care provider. NasalCrom Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about NasalCrom Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More NasalCrom resources NasalCrom Side Effects (in more detail) NasalCrom Use in Pregnancy & Breastfeeding NasalCrom Support Group 0 Reviews for NasalCrom - Add your own review/rating Compare NasalCrom with other medications Hay Fever

Read More:

NasalCrom Solution

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