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