HappeningToo topic
Finasteride reports
Browse community reports connected to Finasteride. These reports can show that other people are describing similar experiences, but they do not prove that Finasteride 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.
40 problems
Abdominal Discomfort while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and abdominal discomfort appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and abdominal pain upper appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and abdominal pain appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and acid reflux appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and alopecia appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and anxiety appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and back pain appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and constipation appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and cough appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and decreased appetite appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and dehydration appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and diarrhea appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and dizziness appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Skin while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and dry skin appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and fatigue appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and feeling abnormal appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and headache appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and hypotension appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and insomnia appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and itching appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Libido Decreased while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and libido decreased appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and malaise appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and muscle spasms appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and muscular weakness appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and myalgia appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and nausea appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and pain appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and palpitations appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and peripheral swelling appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and rash appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and shortness of breath appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and sleep disorder appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and sleepiness appear together. This does not establish that Finasteride 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 Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and tingling or pins and needles appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and tremor appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and vision blurred appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and vomiting appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and weakness appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and weight decreased appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Finasteride
FDA FAERS contains adverse-event reports in which Finasteride and weight increased appear together. This does not establish that Finasteride caused the reported reaction and cannot be used to estimate how often it occurs.
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