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Paclitaxel (aibumin-bound) reports
Browse community reports connected to Paclitaxel (aibumin-bound). These reports can show that other people are describing similar experiences, but they do not prove that Paclitaxel (aibumin-bound) 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.
32 problems
Abdominal Pain Upper while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and abdominal pain upper appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and abdominal pain appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and alopecia appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and back pain appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and chest discomfort appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and chills appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and constipation appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and cough appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and decreased appetite appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and dehydration appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and diarrhea appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and dizziness appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and excessive sweating appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and fatigue appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Hot while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and feeling hot appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Flushing while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and flushing appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and headache appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and hypotension appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and itching appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and malaise appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and myalgia appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and nausea appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and pain appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and peripheral swelling appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and rash appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and shortness of breath appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and skin redness appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Tachycardia while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and tachycardia appear together. This does not establish that Paclitaxel (aibumin-bound) 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 Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and tingling or pins and needles appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and vomiting appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and weakness appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Paclitaxel (aibumin-bound)
FDA FAERS contains adverse-event reports in which Paclitaxel (aibumin-bound) and weight decreased appear together. This does not establish that Paclitaxel (aibumin-bound) caused the reported reaction and cannot be used to estimate how often it occurs.
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