HappeningToo topic
Baclofen reports
Browse community reports connected to Baclofen. These reports can show that other people are describing similar experiences, but they do not prove that Baclofen 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 Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and abdominal discomfort appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and abdominal pain upper appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and abdominal pain appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and acid reflux appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and alopecia appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and anxiety appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and back pain appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Burning Sensation while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and burning sensation appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and chills appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and constipation appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and cough appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and decreased appetite appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and dehydration appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and diarrhea appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and dizziness appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and excessive sweating appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and fatigue appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and feeling abnormal appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Flushing while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and flushing appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and headache appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and hypotension appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Influenza Like Illness while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and influenza like illness appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and insomnia appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and itching appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and malaise appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and migraine appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and muscle spasms appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and muscular weakness appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and myalgia appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and nausea appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and pain appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and peripheral swelling appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and rash appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and shortness of breath appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and skin redness appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and sleepiness appear together. This does not establish that Baclofen 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 Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and tingling or pins and needles appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and tremor appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and vision blurred appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and vomiting appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and weakness appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and weight decreased appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Baclofen
FDA FAERS contains adverse-event reports in which Baclofen and weight increased appear together. This does not establish that Baclofen caused the reported reaction and cannot be used to estimate how often it occurs.
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