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