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Estradiol Gel 0.1% reports

Browse community reports connected to Estradiol Gel 0.1%. These reports can show that other people are describing similar experiences, but they do not prove that Estradiol Gel 0.1% 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.

50 problems

Abdominal Discomfort while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and abdominal discomfort appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Distension while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and abdominal distension appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain Upper while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and abdominal pain upper appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and abdominal pain appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Acid reflux while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and acid reflux appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Alopecia while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and alopecia appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Anxiety while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and anxiety appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Application-site itching while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and application-site itching appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Application-site redness while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and application-site redness appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Back Pain while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and back pain appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Chest Discomfort while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and chest discomfort appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Constipation while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and constipation appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Cough while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and cough appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Decreased Appetite while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and decreased appetite appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and diarrhea appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Dizziness while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and dizziness appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Dyspepsia while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and dyspepsia appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Excessive sweating while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and excessive sweating appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Eye Pain while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and eye pain appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Fatigue while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and fatigue appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Feeling Abnormal while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and feeling abnormal appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Flushing while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and flushing appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Headache while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and headache appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Heart Rate Increased while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and heart rate increased appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Hives while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and hives appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Hot Flush while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and hot flush appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Insomnia while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and insomnia appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Itching while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and itching appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Malaise while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and malaise appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Migraine while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and migraine appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscle Spasms while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and muscle spasms appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscular Weakness while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and muscular weakness appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Myalgia while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and myalgia appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Nausea while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and nausea appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Night Sweats while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and night sweats appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Oropharyngeal Pain while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and oropharyngeal pain appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Pain while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and pain appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Palpitations while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and palpitations appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Peripheral swelling while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and peripheral swelling appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and rash appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Shortness of breath while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and shortness of breath appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Skin redness while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and skin redness appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Sleepiness while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and sleepiness appear together. This does not establish that Estradiol Gel 0.1% 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 Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and tingling or pins and needles appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Tremor while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and tremor appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Vision Blurred while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and vision blurred appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Vomiting while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and vomiting appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Weakness while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and weakness appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Decreased while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and weight decreased appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Increased while using Estradiol Gel 0.1%

FDA FAERS contains adverse-event reports in which Estradiol Gel 0.1% and weight increased appear together. This does not establish that Estradiol Gel 0.1% caused the reported reaction and cannot be used to estimate how often it occurs.

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