Impaired Bioavailability of Famotidine Given Concurrently with a Potent Antacid

Abstract
The effect of a high potency antacid on the oral bioavailability of a single dose of famotidine (40 mg) was evaluated in normal volunteers according to a randomized cross‐over design. Ingestion of the antacid concurrently with famotidine resulted in a significant reduction of peak plasma famotidine concentration (from 156 ± 22 to 104 ± 7, P < 0.05) and area under the famotidine plasma concentration curve (from 956 ± 125 to 607 ± 56, P < 0.02). No significant interaction was observed when the antacid was ingested 2 hours after famotidine administration.

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