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