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The pharmacokinetics and pharmacodynamics of crystalline bromocriptine were studied in healthy volunteers after administration of a single intravenous dose of either 7.5 mg bromocriptine or placebo using a randomized, double-blind, two-period crossover design. Bromocriptine was rapidly absorbed, the median time to maximum concentration (tmax) occurring at 3 min, while the terminal elimination half-life was brief, lasting for less than one hour. Both the volume of distribution and the total body clearance were slightly greater after administration of bromocriptine than after placebo. The maximum plasma concentration (Cmax) and the time at which the plasma concentration was reached (Tmax) were similar for the two treatments. Bromocriptine was rapidly bound to plasma proteins, and the apparent plasma clearance was linearly related to the fractional protein binding. Bromocriptine was not metabolized in humans to any significant extent. The maximum dopamine concentration in plasma was marginally increased after bromocriptine, while the maximum plasma level of prolactin was slightly increased by bromocriptine. Bromocriptine in doses up to 7.5 mg produced a dose-dependent reduction in heart rate of up to 5 beats/min and in blood pressure of up to 10 mmHg. In comparison, placebo produced effects up to 4 beats/min and 2 mmHg.Samsung makes its first move to recover from the negative reaction following the presentation of the Galaxy Note 7
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