HappeningToo topic
Omeprazole reports
Browse community reports connected to Omeprazole. These reports can show that other people are describing similar experiences, but they do not prove that Omeprazole 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.
44 problems
Abdominal Discomfort while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and abdominal discomfort appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and abdominal distension appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and abdominal pain upper appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and abdominal pain appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and acid reflux appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and alopecia appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and anxiety appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and back pain appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and chest discomfort appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and constipation appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and cough appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and decreased appetite appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and dehydration appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and diarrhea appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and dizziness appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and dyspepsia appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and excessive sweating appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and fatigue appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and feeling abnormal appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and headache appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and heart rate increased appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and hives appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and hypotension appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and insomnia appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and itching appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and malaise appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and muscle spasms appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and muscular weakness appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and myalgia appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and nausea appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and pain appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and palpitations appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and peripheral swelling appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and rash appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and shortness of breath appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and skin redness appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and sleepiness appear together. This does not establish that Omeprazole 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 Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and tingling or pins and needles appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and tremor appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and vision blurred appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and vomiting appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and weakness appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and weight decreased appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Omeprazole
FDA FAERS contains adverse-event reports in which Omeprazole and weight increased appear together. This does not establish that Omeprazole caused the reported reaction and cannot be used to estimate how often it occurs.
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