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Ibuprofen reports
Browse community reports connected to Ibuprofen. These reports can show that other people are describing similar experiences, but they do not prove that Ibuprofen 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.
38 problems
Abdominal Discomfort while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and abdominal discomfort appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and abdominal pain upper appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and abdominal pain appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and alopecia appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and anxiety appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and back pain appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and constipation appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and cough appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and decreased appetite appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and diarrhea appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and dizziness appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and dyspepsia appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and excessive sweating appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and fatigue appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and feeling abnormal appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and headache appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and hives appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and hypotension appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and insomnia appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and itching appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and malaise appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and migraine appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and muscle spasms appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and myalgia appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and nausea appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and pain appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and peripheral swelling appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and rash appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and shortness of breath appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and skin redness appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and sleep disorder appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and sleepiness appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and swelling appear together. This does not establish that Ibuprofen 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 Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and tingling or pins and needles appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and vomiting appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and weakness appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and weight decreased appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Ibuprofen
FDA FAERS contains adverse-event reports in which Ibuprofen and weight increased appear together. This does not establish that Ibuprofen caused the reported reaction and cannot be used to estimate how often it occurs.
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