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