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