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