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Abiraterone Acetate reports
Browse community reports connected to Abiraterone Acetate. These reports can show that other people are describing similar experiences, but they do not prove that Abiraterone Acetate 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 Discomfort while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and abdominal discomfort appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and abdominal pain upper appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and abdominal pain appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and back pain appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and constipation appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and cough appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and decreased appetite appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and dehydration appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and diarrhea appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and dizziness appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and excessive sweating appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and fatigue appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and feeling abnormal appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and headache appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Hot Flush while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and hot flush appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and hypotension appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and insomnia appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and malaise appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and muscle spasms appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and muscular weakness appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and myalgia appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and nausea appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and pain appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and peripheral swelling appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and rash appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and shortness of breath appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and sleepiness appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and swelling appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and vomiting appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and weakness appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and weight decreased appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Abiraterone Acetate
FDA FAERS contains adverse-event reports in which Abiraterone Acetate and weight increased appear together. This does not establish that Abiraterone Acetate caused the reported reaction and cannot be used to estimate how often it occurs.
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