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