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