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