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