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Fulvestrant reports
Browse community reports connected to Fulvestrant. These reports can show that other people are describing similar experiences, but they do not prove that Fulvestrant 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.
36 problems
Abdominal Discomfort while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and abdominal discomfort appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and abdominal pain upper appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and abdominal pain appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and alopecia appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and anxiety appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and back pain appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and chills appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and constipation appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and cough appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and decreased appetite appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and dehydration appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and diarrhea appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and dizziness appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Skin while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and dry skin appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and dyspepsia appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and fatigue appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and feeling abnormal appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and headache appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Hot Flush while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and hot flush appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and insomnia appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and itching appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and malaise appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and muscle spasms appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and myalgia appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and nausea appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and pain appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and peripheral swelling appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and rash appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and shortness of breath appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and skin redness appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and sleepiness appear together. This does not establish that Fulvestrant 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 Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and tingling or pins and needles appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and vomiting appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and weakness appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and weight decreased appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Fulvestrant
FDA FAERS contains adverse-event reports in which Fulvestrant and weight increased appear together. This does not establish that Fulvestrant caused the reported reaction and cannot be used to estimate how often it occurs.
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