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Naproxen Sodium Tablet reports

Browse community reports connected to Naproxen Sodium Tablet. These reports can show that other people are describing similar experiences, but they do not prove that Naproxen Sodium Tablet 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.

44 problems

Abdominal Discomfort while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and abdominal discomfort appear together. This does not establish that Naproxen Sodium Tablet 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 Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and abdominal pain upper appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and abdominal pain appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Acid reflux while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and acid reflux appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Alopecia while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and alopecia appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Anxiety while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and anxiety appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Back Pain while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and back pain appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Chills while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and chills appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Constipation while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and constipation appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Cough while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and cough appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Decreased Appetite while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and decreased appetite appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Dehydration while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and dehydration appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and diarrhea appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Dizziness while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and dizziness appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Dyspepsia while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and dyspepsia appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Excessive sweating while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and excessive sweating appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Fatigue while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and fatigue appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Feeling Abnormal while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and feeling abnormal appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Flushing while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and flushing appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Headache while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and headache appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Hives while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and hives appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Insomnia while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and insomnia appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Itching while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and itching appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Malaise while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and malaise appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Migraine while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and migraine appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscle Spasms while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and muscle spasms appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscular Weakness while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and muscular weakness appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Myalgia while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and myalgia appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Nausea while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and nausea appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Pain while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and pain appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Palpitations while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and palpitations appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Peripheral swelling while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and peripheral swelling appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and rash appear together. This does not establish that Naproxen Sodium Tablet 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 Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and shortness of breath appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Skin redness while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and skin redness appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Sleepiness while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and sleepiness appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Swelling while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and swelling appear together. This does not establish that Naproxen Sodium Tablet 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 Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and tingling or pins and needles appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Tremor while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and tremor appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Vision Blurred while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and vision blurred appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Vomiting while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and vomiting appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Weakness while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and weakness appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Decreased while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and weight decreased appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Increased while using Naproxen Sodium Tablet

FDA FAERS contains adverse-event reports in which Naproxen Sodium Tablet and weight increased appear together. This does not establish that Naproxen Sodium Tablet caused the reported reaction and cannot be used to estimate how often it occurs.

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