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