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3 The adverse drug reaction incidence rate was 1.6% (1/64 cases) in the placebo group and 7.7% (5/65 cases) in the mecobalamin 50 mg group

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The results of pharmacokinetic analyses performed in normal volunteers show that following 4 mg SC, a peak plasma level 3 ng/mL (2.4 nmol/L) was obtained with a terminal half-life of 20 min (21)

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