Drug Class:
Proton Pump Inhibitor (PPI)
Mechanism of Action:
Pantoprazole inhibits the H⁺/K⁺ ATPase enzyme (proton pump) located on the gastric parietal cells of the stomach. By blocking this enzyme, it reduces gastric acid secretion, thereby increasing gastric pH.
Indications (Clinical Uses):
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Gastroesophageal reflux disease (GERD)
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Peptic ulcer disease (PUD)
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Zollinger-Ellison syndrome (gastrin-secreting tumor causing hyperacidity)
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Erosive esophagitis
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Stress ulcer prophylaxis (in ICU patients)
Side Effects:
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Headache, nausea, abdominal pain, flatulence
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Long-term use may cause:
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Vitamin B12 deficiency
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Hypomagnesemia
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Increased risk of fractures (due to calcium malabsorption)
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Possible increased risk of infections such as C. difficile or pneumonia due to reduced acid defense
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Drug Interactions:
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Can decrease absorption of drugs that require an acidic environment (e.g., ketoconazole, iron supplements).
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May reduce activation of clopidogrel, an antiplatelet drug, since both are metabolized by CYP2C19 enzymes.
Contraindications:
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Hypersensitivity to PPIs
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Caution in patients with liver disease or those on multiple CYP-metabolized medications.
Clinical Notes:
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Best taken before meals, preferably in the morning.
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Do not crush or chew the delayed-release tablet.
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For GERD or peptic ulcer, treatment usually lasts 4–8 weeks.
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Taper off gradually to avoid rebound acid hypersecretion.
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