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Pantoprazole Sodium

Pfizer · FDA-approved approved Small molecule Quality 69/100

Pantoprazole suppresses gastric acid by covalently binding the (H+, K+)-ATPase enzyme at parietal cells.

Pantoprazole sodium is a proton pump inhibitor indicated for GERD with erosive esophagitis and pathological hypersecretory conditions in adults, with a short one-hour half-life and extensive hepatic metabolism. The drug demonstrates strong efficacy with common adverse reactions including headache, diarrhea, and nausea occurring in >2% of patients. Major contraindications include hypersensitivity to benzimidazoles and concurrent use with rilpivirine-containing antiretrovirals, with significant interactions requiring monitoring for warfarin and other antiretrovirals. Long-term use requires monitoring for serious adverse effects including hypomagnesemia, bone fracture risk, and Clostridioides difficile-associated diarrhea.

At a glance

Generic namePantoprazole Sodium
SponsorPfizer
Drug classProton pump inhibitor (PPI)
Target(H+, K+)-ATPase enzyme
ModalitySmall molecule
Therapeutic areaGastroenterology
PhaseFDA-approved
First approval2000

Mechanism of action

Pantoprazole is a proton pump inhibitor that works by covalently binding to the (H+, K+)-ATPase enzyme system located at the secretory surface of gastric parietal cells. This binding suppresses the final step in gastric acid production, leading to inhibition of both basal and stimulated gastric acid secretion regardless of the stimulus. The antisecretory effect persists longer than 24 hours for all tested doses ranging from 20 mg to 120 mg, providing sustained acid suppression.

Approved indications

Common side effects

Serious adverse events

Drug interactions

Patents

PatentExpiryType

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
FDA Orange BookPatents + exclusivity

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