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Nivolumab reports
Browse community reports connected to Nivolumab. These reports can show that other people are describing similar experiences, but they do not prove that Nivolumab 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.
25 problems
Abdominal Pain while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and abdominal pain appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and back pain appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and chills appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and constipation appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and cough appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and decreased appetite appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and dehydration appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and diarrhea appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and dizziness appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and fatigue appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and headache appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and hypotension appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and itching appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and malaise appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and muscular weakness appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and myalgia appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and nausea appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and pain appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and peripheral swelling appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and rash appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and shortness of breath appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and skin redness appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and vomiting appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and weakness appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Nivolumab
FDA FAERS contains adverse-event reports in which Nivolumab and weight decreased appear together. This does not establish that Nivolumab caused the reported reaction and cannot be used to estimate how often it occurs.
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