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Estradiol reports
Browse community reports connected to Estradiol. These reports can show that other people are describing similar experiences, but they do not prove that Estradiol 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.
51 problems
Abdominal Discomfort while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and abdominal discomfort appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and abdominal distension appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and abdominal pain upper appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and abdominal pain appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and acid reflux appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and alopecia appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and anxiety appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Application Site Irritation while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and application site irritation appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Application Site Pain while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and application site pain appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Application Site Rash while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and application site rash appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Application-site itching while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and application-site itching appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Application-site redness while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and application-site redness appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and back pain appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and chest discomfort appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and constipation appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and cough appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and decreased appetite appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and diarrhea appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and dizziness appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and dyspepsia appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and excessive sweating appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and fatigue appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and feeling abnormal appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and headache appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and heart rate increased appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and hives appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Hot Flush while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and hot flush appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and insomnia appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and itching appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and malaise appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and migraine appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and muscle spasms appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and muscular weakness appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and myalgia appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and nausea appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Night Sweats while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and night sweats appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Oropharyngeal Pain while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and oropharyngeal pain appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and pain appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and palpitations appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and peripheral swelling appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and rash appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and shortness of breath appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and skin redness appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and sleepiness appear together. This does not establish that Estradiol 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 Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and tingling or pins and needles appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and tremor appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and vision blurred appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and vomiting appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and weakness appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and weight decreased appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Estradiol
FDA FAERS contains adverse-event reports in which Estradiol and weight increased appear together. This does not establish that Estradiol caused the reported reaction and cannot be used to estimate how often it occurs.
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