Label: isopto cetamide- sulfacetamide sodium solution

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 3, 2006

If you are a consumer or patient please visit this version.

  • N/A - Section Title Not Found In Database

  • DESCRIPTION

    ISOPTO CETAMIDE® (sulfacetamide sodium ophthalmic solution, USP) 15% is a sterile topical antibacterial agent for ophthalmic use. The active ingredient is represented by the following structural formula:

    Image from Drug Label Content

    Chemical name: N-Sulfanilylacetamide monosodium salt monohydrate

    Each mL contains: Active: Sulfacetamide sodium 150 mg (15%). Preservatives: Methylparaben 0.05%, Propylparaben 0.01%. Vehicle: Hydroxypropyl Methylcellulose 2910 0.5%. Inactives: Sodium Thiosulfate, Dibasic Sodium Phosphate and/or Monobasic Sodium Phosphate (to adjust pH), Purified Water. pH range between 7.0 and 7.8.         DM-02

  • CLINICAL PHARMACOLOGY

    Microbiology

    The sulfonamides are bacteriostatic agents and the spectrum of activity is similar for all. Sulfonamides inhibit bacterial synthesis of dihydrofolic acid by preventing the condensation of the pteridine with aminobenzoic acid through competitive inhibition of the enzyme dihydropteroate synthetase. Resistant strains have altered dihydropteroate synthetase with reduced affinity for sulfonamides or produce increased quantities of aminobenzoic acid.

    Topically applied sulfonamides are considered active against susceptible strains of the following common bacterial eye pathogens: Escherichia coli, Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus (viridans group), Haemophilus influenzae, Klebsiella species, and Enterobacter species.

    Topically applied sulfonamides do not provide adequate coverage against Neisseria species, Serratia marcescens and Pseudomonas aeruginosa. A significant percentage of Staphylococcal isolates are completely resistant to sulfa drugs.

  • INDICATIONS AND USAGE

    For the treatment of conjunctivitis and other superficial ocular infections due to susceptible microorganisms and as an adjunctive in systemic sulfonamide therapy of trachoma:

    Escherichia coli, Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus (viridans group), Haemophilus influenzae, Klebsiella species, and Enterobacter species.

  • CONTRAINDICATIONS

    Hypersensitivity to sulfonamides or to any ingredient of the preparation.

  • WARNINGS

    FOR TOPICAL EYE USE ONLY – NOT FOR INJECTION.

    FATALITIES HAVE OCCURRED, ALTHOUGH RARELY, DUE TO SEVERE REACTIONS TO SULFONAMIDES INCLUDING STEVENS-JOHNSON SYNDROME, TOXIC EPIDERMAL NECROLYSIS, FULMINANT HEPATIC NECROSIS, AGRANULOCYTOSIS, APLASTIC ANEMIA AND OTHER BLOOD DYSCRASIAS.

    Sensitizations may recur when a sulfonamide is readministered, irrespective of the route of administration. Sensitivity reactions have been reported in individuals with no prior history of sulfonamide hypersensitivity. At the first sign of hypersensitivity, skin rash or other serious reaction, discontinue use of this preparation.

  • PRECAUTIONS

    General

    Prolonged use of topical antibacterial agents may give rise to overgrowth of nonsusceptible organisms including fungi. Bacterial resistance to sulfonamides may also develop. The effectiveness of sulfonamides may be reduced by the para-aminobenzoic acid present in purulent exudates.

    Sensitization may recur when a sulfonamide is readministered irrespective of the route of administration, and cross-sensitivity between different sulfonamides may occur.

    At the first sign of hypersensitivity, increase in purulent discharge, or aggravation of inflammation or pain, the patient should discontinue use of the medication and consult a physician (see WARNINGS).

    Information for patients

    To avoid contamination, do not touch tip of container to eye, eyelid or any surface.

    Drug Interactions

    Sulfacetamide preparations are incompatible with silver preparations.

    Carcinogenesis, Mutagenesis, Impairment of Fertility

    No studies have been conducted in animals or in humans to evaluate the possibility of these effects with ocularly administered sulfacetamide. Rats appear to be especially susceptible to the goitrogenic effects of sulfonamides, and long-term oral administration of sulfonamides has resulted in thyroid malignancies in these animals.

    Pregnancy

    Pregnancy Category C. Animal reproduction studies have not been conducted with sulfonamide ophthalmic preparations. Kernicterus may occur in the newborn as a result of treatment of a pregnant woman at term with orally administered sulfonamides. There are no adequate and well controlled studies of sulfonamide ophthalmic preparations in pregnant women and it is not known whether topically applied sulfonamides can cause fetal harm when administered to a pregnant woman. This product should be used in pregnancy only if the potential benefit justifies the potential risk to the fetus.

    Nursing Mothers

    Systemically administered sulfonamides are capable of producing kernicterus in infants of lactating women. Because of the potential for the development of kernicterus in neonates, a decision should be made whether to discontinue nursing or discontinue the drug taking into account the importance of the drug to the mother.

    Pediatric Use

    Safety and effectiveness in pediatric patients below the age of two months have not been established.

  • ADVERSE REACTIONS

    Bacterial and fungal corneal ulcers have developed during treatment with sulfonamide ophthalmic preparations.

    The most frequently reported reactions are local irritation, stinging and burning. Less commonly reported reactions include non-specific conjunctivitis, conjunctival hyperemia, secondary infections and allergic reactions.

    Fatalities have occurred, although rarely, due to severe reactions to sulfonamides including Stevens-Johnson syndrome, toxic epidermal necrolysis, fulminant hepatic necrosis, agranulocytosis, aplastic anemia, and other blood dyscrasias (see WARNINGS).

  • DOSAGE AND ADMINISTRATION

    For conjunctivitis and other superficial ocular infections

    Instill one or two drops into the conjunctival sac(s) of the affected eye(s) every two to three hours initially. Dosages may be tapered by increasing the time interval between doses as the condition responds. The usual duration of treatment is seven to ten days.

    For Trachoma

    Instill two drops into the conjunctival sac(s) of the affected eye(s) every two hours. Topical administration must be accompanied by systemic administration.

  • HOW SUPPLIED

    15 mL in plastic DROP-TAINER® Dispenser.

    15 mL solution –NDC 0998-0522-15

    STORAGE: – Store at 8° - 24°C (46° - 75°F). Protect from light. Do not use if solution is discolored (dark brown). Sulfonamide solutions, on long standing, will darken in color and should be discarded.

    CAUTION: Federal ( USA) law prohibits dispensing without prescription.

    ALCON ( Puerto Rico) INC.

    Humacao, Puerto Rico 00791 USA

    Printed in USA

    236035-0697

  • INGREDIENTS AND APPEARANCE
    ISOPTO CETAMIDE 
    sulfacetamide sodium solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0998-0522
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    sulfacetamide sodium (UNII: 4NRT660KJQ) (sulfacetamide - UNII:4965G3J0F5) 150 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    methylparaben (UNII: A2I8C7HI9T) 0.5 mg  in 1 mL
    propylparaben (UNII: Z8IX2SC1OH) 0.1 mg  in 1 mL
    hydroxypropyl methylcellulose 2910 () 5 mg  in 1 mL
    sodium thiosulfate (UNII: HX1032V43M)  
    dibasic sodium phosphate (UNII: GR686LBA74)  
    monobasic sodium phosphate (UNII: 3980JIH2SW)  
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0998-0522-1515 mL in 1 BOTTLE, PLASTIC
    Labeler - ALCON INC.