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