rifampin
enUKri·fam·pin
R0241350 (rĭ-făm′pĭn)Noun | 1. | rifampin - an antibacterial drug (trade names Rifadin and Rimactane) used to treat tuberculosis |
单词 | rifampin | |||
释义 | rifampinenUKri·fam·pinR0241350 (rĭ-făm′pĭn)
rifampinenUKrifampin(rĭfăm`pĭn), antibioticantibiotic,any of a variety of substances, usually obtained from microorganisms, that inhibit the growth of or destroy certain other microorganisms. Types of Antibiotics ..... Click the link for more information. used in the treatment of tuberculosistuberculosis (TB), contagious, wasting disease caused by any of several mycobacteria. The most common form of the disease is tuberculosis of the lungs (pulmonary consumption, or phthisis), but the intestines, bones and joints, the skin, and the genitourinary, lymphatic, and ..... Click the link for more information. . It is also used to eliminate the meningococcus microorganism from carriers and to treat leprosyleprosy or Hansen's disease , chronic, mildly infectious malady capable of producing, when untreated, various deformities and disfigurements. It is caused by the rod-shaped bacterium Mycobacterium leprae, first described by G. ..... Click the link for more information. , or Hansen's disease. Rifampin, or rifampicin as it was formerly called, acts by inhibiting protein synthesis in sensitive cells. It is a toxic drug whose side effects include flulike symptoms. Because resistant microorganisms emerge during treatment, rifampin is used along with other drugs, e.g., with isoniazidisoniazid , drug used to treat tuberculosis. Also known as isonicotinic acid hydrazide, isoniazid is the most effective antituberculosis drug currently available. The drug inhibits or kills the tubercle bacilli that cause the disease. ..... Click the link for more information. and ethambutol for tuberculosis treatment and with dapsone and clofazimine in the treatment of leprosy. rifampinenUKrifampin[rif-am´pin]rifampin (rifampicin (UK))Pharmacologic class: Rifamycin derivative Therapeutic class: Antitubercular Pregnancy risk category C ActionInhibits RNA synthesis by blocking RNA transcription in susceptible organisms (mycobacteria and some gram-positive and gram-negative bacteria) AvailabilityCapsules: 150 mg, 300 mg Powder for injection: 600 mg/vial Indications and dosages➣ Tuberculosis Adults: 10 mg/kg/day (up to 600 mg/day) P.O. or I.V. infusion as a single dose Children: 10 to 20 mg/kg/day (up to 600 mg/day) P.O. or I.V. infusion as a single dose ➣ Asymptomatic Neisseria meningitidis carriers Adults: 600 mg P.O. or I.V. infusion b.i.d. for 2 days Children ages 1 month and older: 10 mg/kg/day P.O. or I.V. infusion (up to 600 mg/day) q 12 hours for 2 days Infants younger than 1 month old: 5 mg/kg P.O. or I.V. infusion q 12 hours for 2 days Off-label uses• Mycobacterium avium intracellulare complex infection • Brucellosis • Haemophilus influenzae type B • Severe staphylococcal bone and joint infections • Prosthetic valve endocarditis caused by coagulase-negative staphylococci • Leprosy • Prophylaxis in high-risk close contact of patients with N. meningitidis infections Contraindications• Hypersensitivity to drug or other rifamycin derivatives PrecautionsUse cautiously in: • porphyria • history of hepatic disease • concurrent use of other hepatotoxic drugs • pregnant or breastfeeding patients. Administration• Add 10 ml of sterile water to vial to yield a 60-mg/ml solution for I.V. infusion. • Further dilute in 100 ml of dextrose 5% in water (D5W) and infuse over 30 minutes, or add to 500 ml of D5W and infuse over 3 hours. • Give oral doses with a full glass of water 1 hour before or 2 hours after a meal. • For an adult who can't swallow capsules or for a young child, mix capsule contents with syrup, shake well, and administer. • If patient can't receive dextrose, use normal saline solution to dilute. Don't use other I.V. solutions. Adverse reactionsCNS: ataxia, confusion, drowsiness, fatigue, headache, asthenia, psychosis, generalized numbness EENT: conjunctivitis; discolored tears, saliva, and sputum GI: nausea, vomiting, diarrhea, abdominal cramps, dyspepsia, epigastric distress, flatulence, discolored feces, anorexia, sore mouth and tongue, pseudomembranous colitis GU: discolored urine Hematologic: eosinophilia, transient leukopenia, hemolytic anemia, hemolysis, disseminated intravascular coagulation (DIC), thrombocytopenia Hepatic: jaundice Metabolic: hyperuricemia Musculoskeletal: myalgia, joint pain Respiratory: dyspnea, wheezing Skin: flushing, rash, pruritus, discolored sweat, erythema multiforme, toxic epidermal necrolysis, Stevens-Johnson syndrome Other: flulike symptoms, hypersensitivity reactions including vasculitis InteractionsDrug-drug. Barbiturates, beta-adrenergic blockers, cardiac glycosides, clarithromycin, clofibrate, cyclosporine, dapsone, diazepam, doxycycline, fluoroquinolones (such as ciprofloxacin), haloperidol, levothyroxine, methadone, progestins, quinine, tacrolimus, theophylline, tricyclic antidepressants, zidovudine: increased metabolism of these drugs Chloramphenicol, corticosteroids, disopyramide, efavirenz, estrogens, fluconazole, hormonal contraceptives, itra-conazole, ketoconazole, nevirapine, quinidine, opioid analgesics, oral hypoglycemics, phenytoin, quinidine, ritonavir, theophylline, tocainide, verapamil, warfarin: decreased efficacy of these drugs Delavirdine, indinavir, nelfinavir, saquinavir: decreased blood levels of these drugs Hepatotoxic drugs (including isoniazid, ketoconazole, pyrazinamide): increased risk of hepatotoxicity Drug-diagnostic tests. Alanine aminotransferase, alkaline phosphatase, aspartate aminotransferase, bilirubin, blood urea nitrogen, uric acid: increased levels Dexamethasone suppression test: interference with results Direct Coombs' test: false-positive result Folate, vitamin B12 assay: interference with standard assays Hemoglobin: decreased value Liver function tests: abnormal values (transient) Sulfobromophthalein uptake and excretion test: delayed hepatic uptake and excretion Drug-behaviors. Alcohol use: increased risk of hepatotoxicity Patient monitoring• Monitor kidney and liver function tests, CBC, and uric acid level. See Watch for signs and symptoms of bleeding tendency, especially DIC. • Assess for signs and symptoms of hepatic impairment. • Monitor bowel movements for diarrhea, which may signal pseudomembranous colitis. Patient teaching• Advise patient to take oral dose 1 hour before or 2 hours after meals. If drug causes significant GI upset, instruct him to take it with meals. To further minimize GI upset, teach him to eat small, frequent servings of food and drink plenty of fluids. See Instruct patient to immediately report easy bruising or bleeding, fever, malaise, appetite loss, nausea, vomiting, or yellowing of skin or eyes. • Tell patient drug may color his tears, urine, and other body fluids reddish or brownish orange. Instruct him not to wear contact lenses during therapy, because drug may stain them permanently. • Instruct patient not to drink alcohol. • Caution patient to avoid driving and other hazardous activities until he knows how drug affects concentration and alertness. • As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs, tests, and behaviors mentioned above. rifampin(rĭ-făm′pĭn) alsorifampicin(-pĭ-sĭn)rifampinTuberculosis An anti-TB drug used in Pts with a positive skin test who have been exposed to INH-resistant TB Adverse effects Hepatitis, adverse drug interactions, gastritis. See AIDS. Cf Rifalazil.rifampinenUK
Synonyms for rifampin
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