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