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