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