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