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