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