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Bupropion reports

Browse community reports connected to Bupropion. These reports can show that other people are describing similar experiences, but they do not prove that Bupropion 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.

35 problems

Abdominal Discomfort while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and abdominal discomfort appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain Upper while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and abdominal pain upper appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and abdominal pain appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Acid reflux while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and acid reflux appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Alopecia while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and alopecia appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Anxiety while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and anxiety appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Back Pain while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and back pain appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Constipation while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and constipation appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Cough while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and cough appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Decreased Appetite while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and decreased appetite appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and diarrhea appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Dizziness while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and dizziness appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Excessive sweating while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and excessive sweating appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Fatigue while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and fatigue appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Feeling Abnormal while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and feeling abnormal appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Headache while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and headache appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Hives while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and hives appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Hypotension while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and hypotension appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Insomnia while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and insomnia appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Itching while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and itching appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Malaise while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and malaise appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Migraine while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and migraine appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscle Spasms while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and muscle spasms appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Nausea while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and nausea appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Pain while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and pain appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and rash appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Shortness of breath while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and shortness of breath appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Skin redness while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and skin redness appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Sleepiness while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and sleepiness appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Tachycardia while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and tachycardia appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Tremor while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and tremor appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Vomiting while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and vomiting appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Weakness while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and weakness appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Decreased while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and weight decreased appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Increased while using Bupropion

FDA FAERS contains adverse-event reports in which Bupropion and weight increased appear together. This does not establish that Bupropion caused the reported reaction and cannot be used to estimate how often it occurs.

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