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