Conjugated Estrogens reports

Abdominal Discomfort while using Conjugated Estrogens

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

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Abdominal Distension while using Conjugated Estrogens

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

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Abdominal Pain Upper while using Conjugated Estrogens

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

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Abdominal Pain while using Conjugated Estrogens

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

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Acid reflux while using Conjugated Estrogens

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

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Alopecia while using Conjugated Estrogens

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

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Anxiety while using Conjugated Estrogens

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

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Back Pain while using Conjugated Estrogens

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

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Burning Sensation while using Conjugated Estrogens

FDA FAERS contains adverse-event reports in which Conjugated Estrogens and burning sensation appear together. This does not establish that Conjugated Estrogens caused the reported reaction and cannot be used to estimate how often it occurs.

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Constipation while using Conjugated Estrogens

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

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Cough while using Conjugated Estrogens

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

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Decreased Appetite while using Conjugated Estrogens

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

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Dehydration while using Conjugated Estrogens

FDA FAERS contains adverse-event reports in which Conjugated Estrogens and dehydration appear together. This does not establish that Conjugated Estrogens caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Conjugated Estrogens

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

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Dizziness while using Conjugated Estrogens

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

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Dyspepsia while using Conjugated Estrogens

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

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Excessive sweating while using Conjugated Estrogens

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

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Fatigue while using Conjugated Estrogens

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

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Feeling Abnormal while using Conjugated Estrogens

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

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Headache while using Conjugated Estrogens

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

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Hives while using Conjugated Estrogens

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

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Hot Flush while using Conjugated Estrogens

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

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Insomnia while using Conjugated Estrogens

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

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Itching while using Conjugated Estrogens

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

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Malaise while using Conjugated Estrogens

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

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Migraine while using Conjugated Estrogens

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

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Muscle Spasms while using Conjugated Estrogens

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

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Myalgia while using Conjugated Estrogens

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

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Nausea while using Conjugated Estrogens

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

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Pain while using Conjugated Estrogens

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

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Palpitations while using Conjugated Estrogens

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

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Peripheral swelling while using Conjugated Estrogens

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

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Rash while using Conjugated Estrogens

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

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Shortness of breath while using Conjugated Estrogens

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

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Skin redness while using Conjugated Estrogens

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

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Sleepiness while using Conjugated Estrogens

FDA FAERS contains adverse-event reports in which Conjugated Estrogens and sleepiness appear together. This does not establish that Conjugated Estrogens 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 Conjugated Estrogens

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

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Tremor while using Conjugated Estrogens

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

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Vision Blurred while using Conjugated Estrogens

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

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Vomiting while using Conjugated Estrogens

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

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Weakness while using Conjugated Estrogens

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

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Weight Decreased while using Conjugated Estrogens

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

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Weight Increased while using Conjugated Estrogens

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

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