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Pantoprazole reports
Browse community reports connected to Pantoprazole. These reports can show that other people are describing similar experiences, but they do not prove that Pantoprazole caused a symptom or reaction.
⚕️ Medicine safety note
Community reports do not prove causation, cannot be used to estimate how common a reaction is, and are not medical advice.
35 problems
Abdominal Discomfort while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and abdominal discomfort appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and abdominal pain upper appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and abdominal pain appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and acid reflux appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and alopecia appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and anxiety appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and back pain appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and constipation appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and cough appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and decreased appetite appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and dehydration appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and diarrhea appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and dizziness appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and dyspepsia appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and fatigue appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and headache appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and hives appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and hypotension appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and insomnia appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and itching appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and malaise appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and muscle spasms appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and muscular weakness appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and nausea appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and pain appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and peripheral swelling appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and rash appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and shortness of breath appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and skin redness appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and swelling appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Tingling or pins and needles while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and tingling or pins and needles appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and vomiting appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and weakness appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and weight decreased appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Pantoprazole
FDA FAERS contains adverse-event reports in which Pantoprazole and weight increased appear together. This does not establish that Pantoprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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