G04CA03 - Terazosin |
Propably not porphyrinogenic |
PNP |
Rationale
No data pointing to CYP-interaction. Two references authorised / use with care.
Chemical description
(To be edited, initial data ST OCT 04) Used in hypertrophic prostatic disease, 2-5 mg/d. Quinazoline derivative with selective effect on alpha-1-receptors in the bladder, giving rise to relaxation. Metabolized in the liver by hydrolysis and demethylation. No data pointing to CYP-interaction. South African list: use with care. French list: authorized
IPNet drug reports
Uneventful use reported in 3 patients with acute porphyria.
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