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