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| (Riff-ah-pen-teen) |
| Priftin |
| Class: Anti-infective/Antitubercular |
Action Inhibits DNA-dependent RNA polymerase in susceptible strains of Mycobacterium tuberculosis. Bactericidal for intracellular and extracellular M. tuberculosis organisms.
Indications Treatment of pulmonary tuberculosis in conjunction with ³ 1 other antituberculosis drug to which the isolate is susceptible.
Contraindications Hypersensitivity to any of the rifamycins (rifabutin, rifampin).
ADULTS: PO Intensive phase: 600 mg twice weekly (with an interval of ³ 3 days) for 2 months. Continuation phase: 600 mg once weekly for 4 months. CHILDREN ³ 12 YR: PO Dosing should be similar to adult dosing.
Amitriptyline, azole antifungal agents, barbiturates, buspirone, chloramphenicol, clarithromycin, clofibrate, clozapine, oral contraceptives, corticosteroids, cyclosporine, dapsone, delavirdine, diazepam, digitalis glycosides, disopyramide, doxycycline, erythromycin, fluconazole, fluoroquinolones, haloperidol, indinavir, itraconazole, ketoconazole, levothyroxine, losartan, methadone, mexiletine, morphine, nelfinavir, nifedipine, nortriptyline, ondansetron, phenytoin, progestins, quinidine, quinine, ritonavir, saquinavir, sildenafil, sulfonylureas, tacrolimus, tamoxifen, theophylline, tocainide, toremifene, tricyclic antidepressants, troleandomycin, verapamil, warfarin, zidovudine, zolpidem: Has same interaction potential as rifampin. Potent inducer of hepatic drug metabolizing enzymes. Reduced levels and efficacy of target drugs may occur. Ketoconazole: May reduce rifapentine plasma levels, decreasing the therapeutic effects.
Lab Test Interferences May alter microbiological assays for folate and vitamin B12.
CV: Hypertension. CNS: Headache; dizziness. DERM: Rash; acne; pruritus. GI: Nausea; vomiting; dyspepsia; diarrhea; hemoptysis. GU: Pyuria; proteinuria; hematuria; urinary casts. HEMA: Neutropenia; lymphopenia; anemia; leukopenia; thrombocytosis. HEPA: Increased AST and ALT; hepatitis. OTHER: Anorexia; arthralgia; pain; hyperuricemia.
Pregnancy: Category C. Lactation: Undetermined. Children: Safety and efficacy in children < 12 yr not established. Body fluids: May produce a reddish-orange discoloration of the feces, urine, saliva, sweat, sputum, tears, and other body fluids. Contact lenses may become permanently discolored. Monitoring: Conduct baseline measurements of hepatic enzymes, bilirubin, CBC, and platelet counts. Question patients monthly concerning symptoms of adverse reactions. Follow up on abnormalities, including laboratory tests. Pseudomembranous colitis: Should be considered in patients in whom diarrhea develops.
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