ADVERSE REACTIONS SECTION.


ADVERSE REACTIONS. Nystatin is well tolerated even with prolonged therapy. Oral irritation and sensitization have been reported. (See PRECAUTIONS: General).Gastrointestinal: Diarrhea (including one case of bloody diarrhea), nausea, vomiting, gastrointestinal upset/disturbances.Dermatologic: Rash, including urticaria has been reported rarely. Stevens-Johnson syndrome has been reported very rarely.Other: Tachycardia, bronchospasm, facial swelling, and non-specific myalgia have also been rarely reported.

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION.


Carcinogenesis, Mutagenesis, Impairment of Fertility. No long-term animal studies have been performed to evaluate carcinogenic potential. There also have been no studies to determine mutagenicity or whether this medication affects fertility in males or females.

CLINICAL PHARMACOLOGY SECTION.


CLINICAL PHARMACOLOGY. Pharmacokinetics. Gastrointestinal absorption of nystatin is insignificant. Most orally administered nystatin is passed unchanged in the stool. In patients with renal insufficiency receiving oral therapy with conventional dosage forms, significant plasma concentrations of nystatin may occasionally occur.. Microbiology. Nystatin is both fungistatic and fungicidal in vitro against wide variety of yeasts and yeast-like fungi. Candida albicans demonstrates no significant resistance to nystatin in vitro on repeated subculture in increasing levels of nystatin; other Candida species become quite resistant. Generally, resistance does not develop in vivo. Nystatin acts by binding to sterols in the cell membrane of susceptible Candida species with resultant change in membrane permeability allowing leakage of intracellular components. Nystatin exhibits no appreciable activity against bacteria, protozoa, or viruses.

CONTRAINDICATIONS SECTION.


CONTRAINDICATIONS. The preparation is contraindicated in patients with history of hypersensitivity to any of its components.

DESCRIPTION SECTION.


DESCRIPTION. Nystatin is an antimycotic polyene antibiotic obtained from Streptomyces noursei. Structural formula:Nystatin Oral Suspension, for oral administration, contains 100,000 USP Nystatin Units per mL. Inactive ingredients: alcohol (<= 1% v/v), artificial wild cherry flavor, banana flavor, D&C yellow 10, FD&C red 40, glycerin, USP, magnesium aluminum silicate, methylparaben, NF, potassium phosphate dibasic, USP, propylene glycol, USP, propylparaben, NF, purified water, USP and sucrose 33.5%. May also contain citric acid, USP for pH adjustment.. image description.

DOSAGE & ADMINISTRATION SECTION.


DOSAGE AND ADMINISTRATION. INFANTS: mL (200,000 units) four times daily (in infants and young children, use dropper to place one-half of dose in each side of mouth and avoid feeding for to 10 minutes).NOTE: Limited clinical studies in premature and low birth weight infants indicate that mL four times daily is effective.CHILDREN AND ADULTS: 4-6 mL (400,000 to 600,000 units) four times daily (one-half of dose in each side of mouth). The preparation should be retained in the mouth as long as possible before swallowing.Continue treatment for at least 48 hours after perioral symptoms have disappeared and cultures demonstrate eradication of Candida albicans.

GENERAL PRECAUTIONS SECTION.


General. This medication is not to be used for the treatment of systemic mycoses. Discontinue treatment if sensitization or irritation is reported during use.

HOW SUPPLIED SECTION.


HOW SUPPLIED. Nystatin Oral Suspension, USP, 100,000 USP Nystatin Units per mL, is available as fruit flavored, light creamy yellow, ready-to-use suspension.60 mL bottles with calibrated dropper and Pint (473 mL) bottles.. Storage. Store at 20 to 25C (68 to 77F) [see USP Controlled Room Temperature]. Avoid freezing.

INDICATIONS & USAGE SECTION.


INDICATIONS AND USAGE. Nystatin Oral Suspension is indicated for the treatment of candidiasis in the oral cavity.

NURSING MOTHERS SECTION.


Nursing Mothers. It is not known whether nystatin is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when nystatin is administered to nursing woman.

OVERDOSAGE SECTION.


OVERDOSAGE. Oral doses of nystatin in excess of five million units daily have caused nausea and gastrointestinal upset. There have been no reports of serious toxic effects of superinfections (see CLINICAL PHARMACOLOGY, Pharmacokinetics).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL.


PRINCIPAL DISPLAY PANEL 60 mL Bottle Carton. MGPNDC17856-0538-06 ML ENFIT SYR17856-0538-07 ML ENFIT SYR17856-0537-08 ML ENFIT SYR17856-0537-09 .5 ML ENFIT SYRNYSTATIN ORALSUSPENSION, USP(100,000 unitsper mL)Fruit FlavoredRx Only. image description. image description. image description. image description.

PEDIATRIC USE SECTION.


Pediatric Use. See DOSAGE AND ADMINISTRATION.

PHARMACOKINETICS SECTION.


Pharmacokinetics. Gastrointestinal absorption of nystatin is insignificant. Most orally administered nystatin is passed unchanged in the stool. In patients with renal insufficiency receiving oral therapy with conventional dosage forms, significant plasma concentrations of nystatin may occasionally occur.

PRECAUTIONS SECTION.


PRECAUTIONS. General. This medication is not to be used for the treatment of systemic mycoses. Discontinue treatment if sensitization or irritation is reported during use.. Carcinogenesis, Mutagenesis, Impairment of Fertility. No long-term animal studies have been performed to evaluate carcinogenic potential. There also have been no studies to determine mutagenicity or whether this medication affects fertility in males or females.. Pregnancy. Teratogenic Effects Category C. Animal reproduction studies have not been conducted with nystatin oral suspension. It is also not known whether nystatin oral suspension can cause fetal harm when administered to pregnant woman or can affect reproduction capacity. Nystatin oral suspension should be given to pregnant woman only if clearly needed.. Nursing Mothers. It is not known whether nystatin is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when nystatin is administered to nursing woman.. Pediatric Use. See DOSAGE AND ADMINISTRATION.

PREGNANCY SECTION.


Pregnancy. Teratogenic Effects Category C. Animal reproduction studies have not been conducted with nystatin oral suspension. It is also not known whether nystatin oral suspension can cause fetal harm when administered to pregnant woman or can affect reproduction capacity. Nystatin oral suspension should be given to pregnant woman only if clearly needed.

SPL UNCLASSIFIED SECTION.


(100,000 units per mL)Rx only.

STORAGE AND HANDLING SECTION.


Storage. Store at 20 to 25C (68 to 77F) [see USP Controlled Room Temperature]. Avoid freezing.

TERATOGENIC EFFECTS SECTION.


Teratogenic Effects Category C. Animal reproduction studies have not been conducted with nystatin oral suspension. It is also not known whether nystatin oral suspension can cause fetal harm when administered to pregnant woman or can affect reproduction capacity. Nystatin oral suspension should be given to pregnant woman only if clearly needed.