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