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Leuprolide Acetate reports

Browse community reports connected to Leuprolide Acetate. These reports can show that other people are describing similar experiences, but they do not prove that Leuprolide Acetate 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.

33 problems

Abdominal Distension while using Leuprolide Acetate

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

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Abdominal Pain while using Leuprolide Acetate

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

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Alopecia while using Leuprolide Acetate

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

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Anxiety while using Leuprolide Acetate

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

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Back Pain while using Leuprolide Acetate

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

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Constipation while using Leuprolide Acetate

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

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Cough while using Leuprolide Acetate

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

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Decreased Appetite while using Leuprolide Acetate

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

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Diarrhea while using Leuprolide Acetate

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

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Dizziness while using Leuprolide Acetate

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

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Excessive sweating while using Leuprolide Acetate

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

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Fatigue while using Leuprolide Acetate

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

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Feeling Abnormal while using Leuprolide Acetate

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

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Headache while using Leuprolide Acetate

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

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Hot Flush while using Leuprolide Acetate

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

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Insomnia while using Leuprolide Acetate

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

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Itching while using Leuprolide Acetate

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

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Malaise while using Leuprolide Acetate

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

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Migraine while using Leuprolide Acetate

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

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Muscle Spasms while using Leuprolide Acetate

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

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Muscular Weakness while using Leuprolide Acetate

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

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Myalgia while using Leuprolide Acetate

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

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Nausea while using Leuprolide Acetate

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

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Night Sweats while using Leuprolide Acetate

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

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Pain while using Leuprolide Acetate

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

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Peripheral swelling while using Leuprolide Acetate

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

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Rash while using Leuprolide Acetate

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

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Shortness of breath while using Leuprolide Acetate

FDA FAERS contains adverse-event reports in which Leuprolide Acetate and shortness of breath appear together. This does not establish that Leuprolide Acetate 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 Leuprolide Acetate

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

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Vomiting while using Leuprolide Acetate

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

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Weakness while using Leuprolide Acetate

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

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Weight Decreased while using Leuprolide Acetate

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

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Weight Increased while using Leuprolide Acetate

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

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