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