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