Land: USA
Språk: engelska
Källa: NLM (National Library of Medicine)
ATOVAQUONE (UNII: Y883P1Z2LT) (ATOVAQUONE - UNII:Y883P1Z2LT), PROGUANIL HYDROCHLORIDE (UNII: R71Y86M0WT) (PROGUANIL - UNII:S61K3P7B2V)
Glenmark Pharmaceuticals Inc.,USA
ATOVAQUONE
ATOVAQUONE 250 mg
ORAL
PRESCRIPTION DRUG
Atovaquone and proguanil hydrochloride tablets are indicated for the prophylaxis of Plasmodium falciparum malaria, including in areas where chloroquine resistance has been reported. Atovaquone and proguanil hydrochloride tablets are indicated for the treatment of acute, uncomplicated P. falciparum malaria. Atovaquone and proguanil hydrochloride tablets have been shown to be effective in regions where the drugs chloroquine, halofantrine, mefloquine, and amodiaquine may have unacceptable failure rates, presumably due to drug resistance. Risk Summary Available data from published literature and postmarketing experience with use of atovaquone and proguanil hydrochloride in pregnant women are insufficient to identify a drug-associated risk for major birth defects, miscarriage, or adverse maternal or fetal outcomes. The proguanil component of atovaquone and proguanil hydrochloride tablets acts to inhibit parasitic dihydrofolate reductase; however, pregnant women and females of reproductive potential should cont
Atovaquone and proguanil hydrochloride tablets, containing 250 mg atovaquone, USP and 100 mg proguanil hydrochloride, USP are pinkish brown to brown colored, circular, biconvex beveled edge, film-coated tablets with ‘404’ debossed on one side and ‘G’ debossed on the other side. Atovaquone and proguanil hydrochloride tablets 250 mg / 100 mg NDC 68462-404-01 bottles of 100 tablets NDC 68462-404-67 Carton of 24 tablets (2 x 12 unit-dose). Atovaquone and proguanil hydrochloride pediatric tablets, containing 62.5 mg atovaquone, USP and 25 mg proguanil hydrochloride, USP are pinkish brown to brown colored, circular, biconvex beveled edged, film coated tablets with ‘70’ debossed on one side and ‘G’ debossed on the other side. Atovaquone and proguanil hydrochloride pediatric tablets 62.5 mg / 25 mg NDC 68462-402-01 bottles of 100 tablets. Storage Conditions Store at 25°C (77°F); excursions permitted to 15°C to 30°C (59°F to 86°F) [see USP Controlled Room Temperature].
Abbreviated New Drug Application
ATOVAQUONE AND PROGUANIL HYDROCHLORIDE- ATOVAQUONE AND PROGUANIL HYDROCHLORIDE TABLET, FILM COATED ATOVAQUONE AND PROGUANIL HYDROCHLORIDE PEDIATRIC- ATOVAQUONE AND PROGUANIL HYDROCHLORIDE PEDIATRIC TABLET, FILM COATED GLENMARK PHARMACEUTICALS INC.,USA ---------- HIGHLIGHTS OF PRESCRIBING INFORMATION THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE ATOVAQUONE AND PROGUANIL HYDROCHLORIDE TABLETS SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR ATOVAQUONE AND PROGUANIL HYDROCHLORIDE TABLETS. ATOVAQUONE AND PROGUANIL HYDROCHLORIDE TABLETS, FOR ORAL ADMINISTRATION ATOVAQUONE AND PROGUANIL HYDROCHLORIDE PEDIATRIC TABLETS, FOR ORAL ADMINISTRATION INITIAL U.S. APPROVAL: 2000 INDICATIONS AND USAGE Atovaquone and proguanil hydrochloride tablets are an antimalarial indicated for: • • DOSAGE AND ADMINISTRATION • Prophylaxis (2.1): • • • Treatment (2.2): • • Renal Impairment (2.3): • • DOSAGE FORMS AND STRENGTHS • • CONTRAINDICATIONS • • WARNINGS AND PRECAUTIONS • prophylaxis of _Plasmodium falciparum _malaria, including in areas where chloroquine resistance has been reported. (1.1) treatment of acute, uncomplicated _P. falciparum _malaria. (1.2) Atovaquone and proguanil hydrochloride tablets should be taken with food or a milky drink. Start prophylaxis 1 or 2 days before entering a malaria-endemic area and continue daily during the stay and for 7 days after return. Adults: One adult strength tablet per day. Pediatric Patients: Dosage based on body weight (see Table 1). Adults: Four adult strength tablets as a single daily dose for 3 days. Pediatric Patients: Dosage based on body weight (see Table 2). Do not use for prophylaxis of malaria in patients with severe renal impairment. Use with caution for treatment of malaria in patients with severe renal impairment. Tablets (adult strength): 250 mg atovaquone and 100 mg proguanil hydrochloride. (3) Pediatric tablets: 62.5 mg atovaquone and 25 mg proguanil hydrochloride. (3) Known serious hypersensitivity reactions to atov Läs hela dokumentet