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