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Prednisone reports
Browse community reports connected to Prednisone. These reports can show that other people are describing similar experiences, but they do not prove that Prednisone 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.
31 problems
Abdominal Discomfort while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and abdominal discomfort appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and abdominal pain upper appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and abdominal pain appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and alopecia appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and anxiety appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and back pain appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and constipation appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and cough appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and decreased appetite appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and diarrhea appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and dizziness appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and fatigue appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and feeling abnormal appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and headache appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and hives appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and hypotension appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and insomnia appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and itching appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and malaise appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and muscle spasms appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and nausea appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and pain appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and peripheral swelling appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and rash appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and shortness of breath appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and skin redness appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and swelling appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and vomiting appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and weakness appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and weight decreased appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Prednisone
FDA FAERS contains adverse-event reports in which Prednisone and weight increased appear together. This does not establish that Prednisone caused the reported reaction and cannot be used to estimate how often it occurs.
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