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ranitidine
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(ra NI ti deen)

Drug Interactions

Binds weakly to hepatic CYP isoenzyme system in vitro.

Affinity for CYP isoenzyme system is about 10% that of cimetidine; inhibition of CYP isoenzyme system is 2.4 times less than cimetidine.

Does not inhibit CYP isoenzymes at recommended dosages.

May minimally inhibit hepatic metabolism of some drugs, or affect bioavailability by another mechanism (e.g., pH-dependent absorption, altered volume of distribution).

Specific Drugs, Foods, and Laboratory Tests

Drug, Food, or Test Interaction Comments
Acetaminophen Dose-dependent inhibition of acetaminophen metabolism in vitro
Alcohol Moderate alcohol consumption by individuals receiving concurrent ranitidine unlikely to result in clinically important alterations of blood alcohol concentration and/or alcohol metabolism Controversy about psychomotor impairment potential; observe usual precautions about alcohol intake and hazardous tasks requiring mental alertness or physical coordination
Antacids Low doses (10–15 mEq HCl neutalizing capacity/10 mL) do not appear to decrease absorption or plasma concentrations of ranitidine Higher doses (e.g., 150 mEq HCl neutralizing capacity/30 mL) decrease absorption by 33%, decrease plasma concentrations, and AUC
Atenolol Atenolol pharmacokinetics apparently not affected
Benzodiazepines (e.g., diazepam, lorazepam, midazolam, triazolam)

Diazepam AUC, mean half-life not substantially affected

Lorazepam elimination half-life, volume of distribution, clearance unaffected

Midazolam oral bioavailability may be increased by ranitidine

Triazolam oral bioavailability may be increased by elevated gastric pH clinical importance unknown

Observe carefully for signs of midazolam-induced respiratory and CNS depression; decrease midazolam dosage if required
Food Does not appear to decrease absorption or plasma concentrations of ranitidine
Metoprolol Increased metoprolol AUC, peak serum concentration, elimination half-life
Multistix®, test for urine protein False positive Use sulfosalicylic acid reagent for urinary protein determinations while using ranitidine
Nifedipine Nifedipine AUC increased by 30%
Phenytoin Phenytoin serum concentrations unaffected
Propantheline Appears to delay absorption and increases peak serum concentrations of ranitidine; biovailability increased about 23% with concomitant administration
Propranolol Propranolol mean serum concentrations not substantially affected
Smoking Adversely affects duodenal ulcer healing and decreases ranitidine efficacy; number of cigarettes/day apparently does not influence healing rate
Theophylline Ranitidine appparently does not alter theophylline clearance
Vitamin B12 Vitamin B12 malabsorption and deficiency may occur with long-term ranitidine therapy
Warfarin Increased or decreased PT reported Pharmacokinetic studies: up to 400 mg daily had no effect on warfarin clearance or PT
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