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