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