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