A02BA53 - Famotidine, Combinations |
Propably not porphyrinogenic |
PNP |
Rationale
Famotidine: Partly unmetabolized. No clinical observations pointing to CYP inducing properties. Combined with two inorganic salts without CYP intarective properties
Chemical description
Famotidine: Used in ventricular hyperacidity (H2-receptor antagonist). About 70% excreted in urine in unmetabolized form. Partly metabolized in the liver to inactive sulfoxide metabolite. Impaired liver function does not seem to change the kinetics. Famotidine: South African list: use with care. French list: avoid
IPNet drug reports
Uneventful use reported in 1 patient with acute porphyria.
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