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