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