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