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