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British Journal of Clinical Pharmacology logoLink to British Journal of Clinical Pharmacology
. 2012 Jun 11;74(1):224–225. doi: 10.1111/j.1365-2125.2012.04349.x

Erratum

PMCID: PMC3394152

Ramirez E, Laosa O, Guerra P, Duque B, Mosquera B, Borobia AM, Lei SH, Carcas AJ, Frias J. Br J Clin Pharmacol 2010; 70: 694–702.

In [1], the article states that loratadine is a BCS Class I drug (in Table 1, column 1, line 10; Table 4, column 1, line 14; and page 698, column 1, line 4). Data were obtained from the Therapeutic System Research Laboratories website (at http://www.tsrlinc.com/services/bcs/search.cfm). The new website of Therapeutic System Research Laboratories at http://69.20.123.154/services/bcs/results.cfm yields a page displaying loratadine as Class II and the metabolite desloratadine as Class I (last accessed March 21, 2012).

Table 1.

Biopharmaceutics Classification System (BCS) of active substances (number of studies)

graphic file with name bcp0074-0224-t1.jpg

Table 4.

Results of non-BE formulations (study number of subjects, retrospective sample size calculation) classified by BCS active substances for maximum observed plasma concentration (Cmax) and area under the concentration-time curve (AUC)

graphic file with name bcp0074-0224-t4.jpg

The corrected versions of Table 1 and 4 and the sentence on page 698 are published below.

In one case (sildenafil) the CVIntrasubject was higher than predicted (Group A2 Table 4).

REFERENCE

  1. Ramirez E, Laosa O, Guerra P, Duque B, Mosquera B, Borobia AM, Lei SH, Carcas AJ, Frias J. Acceptability and characteristics of 124 human bioequivalence studies with active substances classified according to the Biopharmaceutic Classification System. Br J Clin Pharmacol. 2010;70:694–702. doi: 10.1111/j.1365-2125.2010.03757.x. [DOI] [PMC free article] [PubMed] [Google Scholar]

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