Reviewed - The BMS-777607 Pros As well as , Downsides

9%) received treatment with gabapentin (brand: 400 [29.2%]; generic: 969 [70.8%]) and 841 with venlafaxine (brand: 370 [44.0%]; generic: Selleck Epigenetics Compound Library 471 [56.0%]). Table 2 shows the demographic characteristics and associated comorbidities for the patients with pNP and GAD. By subgroup (brand, generic), the subjects on treatment with gabapentin had a different proportion of females (56.3% vs 63.2%; P=0.017). With venlafaxine, there were no significant differences in any of the descriptive characteristics. There were no statistically significant differences in the distribution of ICPC/ICD-9 codes for pNP in the gabapentin groups between brand or generic (P=0.969): axial radiculopathies, 56.8% in the brand group and 55.3% in the generic group; any type of neuralgias, 22.3% and 22.7%, respectively; neuropathies, 14.5% and 15.6%, respectively; and other pNP conditions, 6.5% and 6.4%, respectively. Figure 1 General outline of the study. Table 2 Baseline characteristics of study series Table 3 shows the characteristics of medication use. With gabapentin, mean treatment duration was longer for brand than generic (7.3 vs 6.3 months; PEvodiamine vs 79.0%; P=0.045), and treatment persistence time (Figure 2B) were all slightly longer with brand than with generic drug, but statistically significant. The medication prescribed to the patients in the pre-treatment (6 previous months) and treatment (12-month follow-up) periods are shown in Table 4. In the gabapentin group, the average number of concomitant medications administered to patients before receiving the initial brand medication (pre-treatment vs treatment period) decreased significantly in the case of brand (2.3 vs 1.9 drugs; PBMS-777607 research buy P