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