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