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