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