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