Rifampin
Questions | Reviews
rifampin and liver effects
What is the risk of hepatotoxicity with rifampin alone, not with any of the other hepatotoxic meds. Should LFT be monitored and how regularly with doses for bacteria resistent osteomyelitis for about a month.
by greg in rapid city, 06/07/2006
rifampin use in lyme disease with co-infections of h.pylori and bartonella hensalae-
what is the recommended dose and length of treatment for neuro-lyme disease with many co-infections including h.pylori, bartonella hensalae,babesia duncani and rocky mountain spotted fever
by debbieheverly in Niagara Falls, New York, 09/01/2008
Rifampin
I work at a Correctional facility in the state of N.Y.The inmates there that are taking rifampin are all testing postive for opioids when drug tested. Is there a reason for this? Could you please email me back and tell me if there is a reason for this...
by Marleen in Fayville N.Y. 13066 USA, 01/08/2007
Rifamoin
Sirs: I will be starting on Rifampin on Monday will it be safe to take it as I am allergic to preservatives and certain foods? I read something about this and confused about it.. Thank you so much for a reply
by Joyce Jones in United States, 09/29/2006
My Gastro doctor prescribed Rifampin for itching.
I have Primary Biliary Cirrhosis. I told my Gastroenterologist about increased itching, and he prescribed Rifampin. From what I can tell, it is a drug used for TB. I saw no mention of it being used to control itching. It is the weekend, and I cannot c...
by Carol in Tupelo, MS, 07/29/2006
Classification: Primary antitubercular agent Action/Kinetics: Semisynthetic antibiotic derived from Streptomyces mediterranei. Suppresses RNA synthesis by binding to the beta subunit of DNA-dependent RNA polymerase. This prevents attachment of the enzyme to DNA and blockade of RNA transcription. Both bacteriostatic and bactericidal; most active against rapidly replicating organisms. Well absorbed from the GI tract; widely distributed in body tissues. Peak plasma concentration: 4-32 mcg/mL after 2-4 hr. t 1/2: 1.5-5 hr (higher in clients with hepatic impairment). In normal clients t 1/2 decreases with usage. Metabolized in liver; 60% is excreted in feces. Uses: All types of tuberculosis. Must be used in conjunction with at least one other tuberculostatic drug (such as isoniazid, ethambutol, pyrazinamide) but is the drug of choice for retreatment. Also for treatment of asymptomatic meningococcal carriers to eliminate Neisseria meningitidis. Investigational: Used in combination for infections due to Staphylococcus aureus and S. epidermidis (endocarditis, osteomyelitis, prostatitis); Legionnaire's disease; in combination with dapsone for leprosy; prophylaxis of meningitis due to Haemophilus influenzae and gram-negative bacteremia in infants. Contraindications: Hypersensitivity; not recommended for intermittent therapy. Special Concerns: Safe use during lactation has not been established. Safety and effectiveness not determined in children less than 5 years of age. Use with extreme caution in clients with hepatic dysfunction. Side Effects: GI: N&V;, diarrhea, anorexia, gas, pseudomembranous colitis, pancreatitis, sore mouth and tongue, cramps, heartburn, flatulence. CNS: Headache, drowsiness, fatigue, ataxia, dizziness, confusion, generalized numbness, fever, difficulty in concentrating. Hepatic: Jaundice, hepatitis. Increases in AST, ALT, bilirubin, alkaline phosphatase. Hematologic: Thrombocytopenia, eosinophilia, hemolysis, leukopenia, hemolytic anemia. Allergic: Flu-like symptoms, dyspnea, wheezing, SOB, purpura, pruritus, urticaria, skin rashes, sore mouth and tongue, conjunctivitis. Renal: Hematuria, hemoglobinuria, renal insufficiency, acute renal failure. Miscellaneous: Visual disturbances, muscle weakness or pain, arthralgia, decreased BP, osteomalacia, menstrual disturbances, edema of face and extremities, adrenocortical insufficiency, increases in BUN and serum uric acid. NOTE: Body fluids and feces may be red-orange. Laboratory Test Alterations: AST, ALT, alkaline phosphatase, BUN, bilirubin, uric acid, BSP retention values. False + Coombs' test. Overdose Management: Symptoms: Shortly after ingestion, N&V;, and lethargy will occur. Followed by severe hepatic involvement (liver enlargement with tenderness, increased direct and total bilirubin, change in hepatic enzymes) with unconsciousness. Also, brownish red or orange discoloration of urine, saliva, tears, sweat, skin, and feces. Treatment: Gastric lavage followed by activated charcoal slurry introduced into the stomach. Antiemetics to control N&V.; Forced diuresis to enhance excretion. If hepatic function is seriously impaired, bile drainage may be required. Extracorporeal hemodialysis may be necessary.
Drug Interactions:
How Supplied: Capsule: 150 mg, 300 mg; Powder for injection: 600 mg
Dosage
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