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