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