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trimethoprim/polymyxin B ophthalmic (Polytrim Ophthalmic Solution)

 

Classes: Antibiotics, Ophthalmic Combos

Dosing and uses of Polytrim Ophthalmic Solution (trimethoprim/polymyxin B ophthalmic)

 

Adult dosage forms and strengths

trimethoprim/polymyxin B

ophthalmic solution

  • (1mg/10,000 units)/mL

 

Bacterial Conjunctivitis

Indicated in the treatment of surface ocular bacterial infections, including acute bacterial conjunctivitis and blepharoconjunctivitis

Instill 1 gtt in affected eye(s) q3hr for 7-10 days; not to exceed 6 doses/day

 

Pediatric dosage forms and strengths

trimethoprim/polymyxin B

ophthalmic solution

  • (1mg/10,000 units)/mL

 

Bacterial Conjunctivitis

Indicated in the treatment of surface ocular bacterial infections, including acute bacterial conjunctivitis and blepharoconjunctivitis

<2 months: Safety and efficacy not established

≥2 years: Instill 1 gtt in affected eye(s) q3hr for 7-10 days; not to exceed 6 doses/day

 

Polytrim Ophthalmic Solution (trimethoprim/polymyxin B ophthalmic) adverse (side) effects

Frequency not defined

Local irritation consisting of increased redness, burning, stinging, and/or itching

Hypersensitivity reactions consisting of lid edema, itching, increased redness, tearing, and/or circumocular rash

 

Warnings

Contraindications

Hypersensitivity

 

Cautions

Not for injection into the eye Not indicated for prophylaxis or treatment of ophthalmia neonatorum

Prolonged use may result in overgrowth of nonsusceptible organisms

Avoid contaminating applicator tip with material from the eye, fingers, or other source

If redness, irritation, swelling or pain persists or increases, discontinue use immediately and seek medical attention

Advise patient to not to wear contact lenses with active signs and symptoms of ocular bacterial infections or while using antibacterial eyedrops

 

Pregnancy and lactation

Pregnancy category: C

Lactation: Unknown whether distributed in breast milk

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Polytrim Ophthalmic Solution (trimethoprim/polymyxin B ophthalmic)

Mechanism of action

Polymyxin B: Bactericidal; causes leakage of bacterial membrane by binding to phospholipids

Trimethoprim: Bactericidal; blocks production of tetrahydrofolic acid from dihydrofolic acid by binding to and reversibly inhibiting the enzyme dihydrofolate reductas

Indicated for ocular infections caused by susceptible strains of the following microorganisms: Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pneumoniae, Streptococcus viridans, Haemophilus influenzae, and Pseudomonas aeruginosa