Treatment of Mycobacterial infections Flashcards
Isoniazid, Rifampin, Pyrazinamide and Ethambutol are first line drugs for this condition
Tuberculosis
First line drug for tuberculosis that inhibits lipid (mycolic acid) synthesis required for cell wall integrity
Isoniazid
MOA of Isoniazid
Inhibits mycolic acid synthesis required for cell wall integrity
Isoniazid is inactivated by genetically determined ______
Acetylation
(Acetyl isoniazid may be converted to acetyl hydrazide, then to a hepatotoxic metabolite)
Tuberculosis drug that is inactivated by genetically determined acetylation
Isoniazid
Neurotoxicity from Isoniazid may be minimized by administration of this
Pyridoxine (vit b6)
Pyridoxine (B6) may minimize this adverse effect of Isoniazid
Neurotoxicity
Pyridoxine (B6) may minimize nephrotoxicity of this tuberculosis drug
Isoniazid
High acetylators have higher risk of this adverse effect of Isoniazid
Hepatotoxicity
Isoniazid use should be avoided if there is a five fold increase in this in normal individuals or three fold increase in patients with symptoms of hepatitis
Serum aspartate aminotransferase
Neurotoxicity, hepatotoxicity, and hemolysis in patients with G6PD deficiency are adverse effects of this tuberculosis drug
Isoniazid
Primary toxicity of Ethionamide
Neurological disruption
Tuberculosis drug with neurological disruption as a primary toxicity
Ethionamide
Tuberculosis drug that inhibits arabinogalactan polymerization by inhibition of arabinosyl transferase, thereby disrupting cell wall synthesis
Ethambutol
Ethambutol inhibits this enzyme
Arabinosyl transferase
thus inhibits arabinogalactan polymerization