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Nilotinib reports
Browse community reports connected to Nilotinib. These reports can show that other people are describing similar experiences, but they do not prove that Nilotinib 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.
36 problems
Abdominal Discomfort while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and abdominal discomfort appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and abdominal pain upper appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and abdominal pain appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and alopecia appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and anxiety appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and back pain appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and chills appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and constipation appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and cough appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and decreased appetite appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and diarrhea appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and dizziness appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Skin while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and dry skin appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and dyspepsia appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Eye Pain while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and eye pain appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and fatigue appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and feeling abnormal appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and headache appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and insomnia appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and itching appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and malaise appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and muscle spasms appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and myalgia appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and nausea appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and pain appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and palpitations appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and peripheral swelling appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and rash appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and shortness of breath appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and sleepiness appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Tachycardia while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and tachycardia appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and vision blurred appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and vomiting appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and weakness appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and weight decreased appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Nilotinib
FDA FAERS contains adverse-event reports in which Nilotinib and weight increased appear together. This does not establish that Nilotinib caused the reported reaction and cannot be used to estimate how often it occurs.
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