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Lamotrigine Extended-release reports

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

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

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Abdominal Pain while using Lamotrigine Extended-release

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

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Acid reflux while using Lamotrigine Extended-release

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

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Alopecia while using Lamotrigine Extended-release

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

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Anxiety while using Lamotrigine Extended-release

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

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Constipation while using Lamotrigine Extended-release

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

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Cough while using Lamotrigine Extended-release

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

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Decreased Appetite while using Lamotrigine Extended-release

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

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Diarrhea while using Lamotrigine Extended-release

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

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Dizziness while using Lamotrigine Extended-release

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

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Fatigue while using Lamotrigine Extended-release

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

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Feeling Abnormal while using Lamotrigine Extended-release

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

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Headache while using Lamotrigine Extended-release

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

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Hives while using Lamotrigine Extended-release

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

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Hypotension while using Lamotrigine Extended-release

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

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Insomnia while using Lamotrigine Extended-release

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

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Irritability while using Lamotrigine Extended-release

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

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Itching while using Lamotrigine Extended-release

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

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Malaise while using Lamotrigine Extended-release

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

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Migraine while using Lamotrigine Extended-release

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

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Muscle Spasms while using Lamotrigine Extended-release

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

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Muscular Weakness while using Lamotrigine Extended-release

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

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Nausea while using Lamotrigine Extended-release

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

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Pain while using Lamotrigine Extended-release

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

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Rash while using Lamotrigine Extended-release

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

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Shortness of breath while using Lamotrigine Extended-release

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

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Skin redness while using Lamotrigine Extended-release

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

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Sleep Disorder while using Lamotrigine Extended-release

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

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Sleepiness while using Lamotrigine Extended-release

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

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Tachycardia while using Lamotrigine Extended-release

FDA FAERS contains adverse-event reports in which Lamotrigine Extended-release and tachycardia appear together. This does not establish that Lamotrigine Extended-release 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 Extended-release

FDA FAERS contains adverse-event reports in which Lamotrigine Extended-release and tingling or pins and needles appear together. This does not establish that Lamotrigine Extended-release caused the reported reaction and cannot be used to estimate how often it occurs.

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Tremor while using Lamotrigine Extended-release

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

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Vision Blurred while using Lamotrigine Extended-release

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

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Vomiting while using Lamotrigine Extended-release

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

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Weakness while using Lamotrigine Extended-release

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

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Weight Decreased while using Lamotrigine Extended-release

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

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Weight Increased while using Lamotrigine Extended-release

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

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