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Diclofenac Sodium 1% reports
Browse community reports connected to Diclofenac Sodium 1%. These reports can show that other people are describing similar experiences, but they do not prove that Diclofenac Sodium 1% 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.
24 problems
Abdominal Discomfort while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and abdominal discomfort appear together. This does not establish that Diclofenac Sodium 1% 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 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and abdominal pain upper appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and alopecia appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and decreased appetite appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and diarrhea appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and dizziness appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Mouth while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and dry mouth appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and dyspepsia appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and fatigue appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and headache appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and hives appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and insomnia appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and itching appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and malaise appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and muscle spasms appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and nausea appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and pain appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and rash appear together. This does not establish that Diclofenac Sodium 1% 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 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and shortness of breath appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and sleep disorder appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and swelling appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and vomiting appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and weakness appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Diclofenac Sodium 1%
FDA FAERS contains adverse-event reports in which Diclofenac Sodium 1% and weight increased appear together. This does not establish that Diclofenac Sodium 1% caused the reported reaction and cannot be used to estimate how often it occurs.
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