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