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