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