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