Cimetidine Hydrochloride has 10 known drug interactions based on U.S. FDA drug labeling data. 4 are classified as major interactions requiring close medical supervision. Notable interactions include combinations with Lidocaine, Phenytoin, Theophylline. Patients taking Cimetidine Hydrochloride should inform their healthcare provider of all current medications — including over-the-counter drugs and supplements — to avoid potentially harmful combinations. Data sourced from OpenFDA and the NIH National Library of Medicine.
- Total
- 10
- Major
- 4
- Moderate
- 6
Major (4)
- Cimetidine Hydrochloride + Lidocaine— Cimetidine reduces hepatic metabolism of lidocaine, increasing blood levels with reported adverse clinical effects.
- Cimetidine Hydrochloride + Phenytoin— Cimetidine reduces hepatic metabolism of phenytoin, delaying elimination and increasing blood levels with reported adver…
- Cimetidine Hydrochloride + Theophylline— Cimetidine reduces hepatic metabolism of theophylline, increasing blood levels. Adverse clinical effects reported; monit…
- Cimetidine Hydrochloride + Warfarin— Cimetidine reduces hepatic metabolism of warfarin, increasing blood levels and delaying elimination. Clinically signific…
Moderate (6)
- Cimetidine Hydrochloride + Chlordiazepoxide— Cimetidine reduces hepatic metabolism of chlordiazepoxide, delaying elimination and increasing blood levels.
- Cimetidine Hydrochloride + Diazepam— Cimetidine reduces hepatic metabolism of diazepam, delaying elimination and increasing blood levels.
- Cimetidine Hydrochloride + Ketoconazole— Cimetidine-induced pH alteration may affect ketoconazole absorption. Ketoconazole should be given at least 2 hours befor…
- Cimetidine Hydrochloride + Metronidazole— Cimetidine reduces hepatic metabolism of metronidazole, delaying elimination and increasing blood levels.
- Cimetidine Hydrochloride + Nifedipine— Cimetidine reduces hepatic metabolism of nifedipine, delaying elimination and increasing blood levels.
- Cimetidine Hydrochloride + Propranolol— Cimetidine reduces hepatic metabolism of propranolol, delaying elimination and increasing blood levels.