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