คำอธิบาย
Ranitidine can modestly increase diazepam bioavailability by raising gastric pH and weakly inhibiting hepatic CYP2C19-mediated diazepam metabolism.
กลไก
Ranitidine's H2 blockade raises intragastric pH, potentially improving diazepam dissolution and absorption; weak CYP2C19 inhibition further reduces N-desmethyldiazepam formation.
ความสำคัญทางคลินิก
Pharmacokinetic data demonstrate a modest (~25%) increase in diazepam AUC; additional sedation is possible but clinically minor in most patients.
การจัดการ
No dose adjustment required; advise patients on additive sedation and to avoid alcohol; the interaction is less pronounced than with cimetidine.
ข้อจำกัดความรับผิดชอบทางการแพทย์
This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.