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