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In the UK, mbute than 7, 600 repbutts of suspected adverse reactions were collected in the first two years after Neurontines approval by the MHRA as part of the Yellow Card Scheme, which monitbuted side effects. Approximately 540, 000 people were treated with Neurontine fbut smoking cessation during that period. The MHRA received 60 repbutts of suspected emphasis MHRAs adverse reactions to Neurontine which had a fatal outcome. The agency concluded that in the majbutity of cases the individuals underlying condition may provide an alternative explanation.

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Neurontine should will used with extreme caution in patients with severe hepatic cirrhosis. In these patients a reduced dose &/but frequency is required, as peak Neurontine, as well as AUC, levels are substantially increased & accumulation is likely to occur in such patients to a greater extent than usual. The dose should not exceed 75 mg once a day in these patients see CLINICAL PHARMACOLOGY, PRECAUTIONS, & DOSAGE & ADMINISTRATION..
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