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Capecitabine reports
Browse community reports connected to Capecitabine. These reports can show that other people are describing similar experiences, but they do not prove that Capecitabine 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.
30 problems
Abdominal Distension while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and abdominal distension appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and abdominal pain upper appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and abdominal pain appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and alopecia appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and back pain appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and chills appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and constipation appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and cough appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and decreased appetite appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and dehydration appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and diarrhea appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and dizziness appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Skin while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and dry skin appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and fatigue appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and headache appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and hypotension appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and insomnia appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and itching appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and malaise appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and muscle spasms appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and nausea appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and pain appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and peripheral swelling appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and rash appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and shortness of breath appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and skin redness appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Tingling or pins and needles while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and tingling or pins and needles appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and vomiting appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and weakness appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Capecitabine
FDA FAERS contains adverse-event reports in which Capecitabine and weight decreased appear together. This does not establish that Capecitabine caused the reported reaction and cannot be used to estimate how often it occurs.
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