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Nintedanib reports
Browse community reports connected to Nintedanib. These reports can show that other people are describing similar experiences, but they do not prove that Nintedanib 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.
38 problems
Abdominal Discomfort while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and abdominal discomfort appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and abdominal distension appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and abdominal pain upper appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and abdominal pain appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and acid reflux appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and alopecia appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and anxiety appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and back pain appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and chest discomfort appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and constipation appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and cough appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and decreased appetite appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and dehydration appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and diarrhea appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and dizziness appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Mouth while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and dry mouth appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and dyspepsia appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and fatigue appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and feeling abnormal appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Flatulence while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and flatulence appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and headache appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and heart rate increased appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and hypotension appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and insomnia appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and itching appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and malaise appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and muscle spasms appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and nausea appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Oropharyngeal Pain while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and oropharyngeal pain appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and pain appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and peripheral swelling appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and rash appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and shortness of breath appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and sleepiness appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and vomiting appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and weakness appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and weight decreased appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Nintedanib
FDA FAERS contains adverse-event reports in which Nintedanib and weight increased appear together. This does not establish that Nintedanib caused the reported reaction and cannot be used to estimate how often it occurs.
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