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