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