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