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