Rifapentine

A to Z Drug Facts

Rifapentine

  Action
  Indications
  Contraindications
  Route/Dosage
  Interactions
  Lab Test Interferences
  Adverse Reactions
  Precautions
Patient Care Considerations
  Administration/Storage
  Assessment/Interventions
  Patient/Family Education


(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).

 Route/Dosage

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.

 Interactions

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.

 Adverse Reactions

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.

 Precautions

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.


PATIENT CARE CONSIDERATIONS


 Administration/Storage

 Assessment/Interventions

OVERDOSAGE: SIGNS & SYMPTOMS
  Headache, urinary frequency, heartburn, transient elevations of hepatic enzymes

 Patient/Family Education

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Copyright
© 2003 Facts and Comparisons
David S. Tatro
A to Z Drug Facts