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