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