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