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