Active Ingredient: Orlistat
The answer truthfully is nothing.
Gallbladder and renal ultrasound were obtained by standard methodology on all subjects. Dextrose.
Blood samples were collected through a second intravenous line for glucose and insulin at 2, 4, 6, 10, 14, 19, 22, 24, 27, 30, 35, 40, 45, 50, 70, 90, 120, 150, 180, 210, 240, 270, and 300 minutes, and for C-peptide at 120 minute intervals.
Insulin. Insulin sensitivity and glucose effectiveness were assessed according to Bergman's minimal model 47 using the SAAM II program version 1.
Monitoring of adverse events Subjects were queried weekly about adverse events for the first 12 weeks, and monthly thereafter, with particular attention directed toward the expected gastrointestinal effects of orlistat.
In addition, at 3-month intervals, a clinical pharmacist interviewed subjects with a comprehensive questionnaire employing a review-of-systems approach to identify expected and unexpected adverse events 53.
All data were log-transformed before calculation of the geometric mean and standard deviation. Paired, two-tailed T-tests were conducted on the log-transformed data to determine differences between weights, blood lipids, glycemic indices, and other laboratory parameters at baseline versus 6 months of orlistat therapy.
For the preplanned analysis between African-American and Caucasian subjects, data were expressed as the change from baseline due to the large differences in baseline values and analysis of covariance was used to determine the difference in response adjusted for the initial value at baseline.
Post-hoc tests were corrected for multiple comparisons using the Bonferroni-Holm procedure. Data from each variable for which at least one follow-up measurement was available are reported as last observation carried forward.
For log-transformed data, the back-transformed geometric means are reported. Height increased on average by 1. Height, age, and pubertal stage did not differ by race.
One subject cited intolerance of gastrointestinal effects as the reason for withdrawing from the study. Two subjects had stopped taking the medication completely by 5 months of treatment.
African-American subjects reported missing 19. Reasons given for noncompliance with the thrice-daily orlistat regimen were: having skipped a meal e. Fecal fat excretion increased from 5.
Reports of the adverse effects experienced, obtained weekly for the first 3 months of the study period, found the gastrointestinal effects of orlistat were generally mild and transient.
Curioni, and D. A A Weight-loss drugs: Ruiz, and S.
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Not sure at this point. Xenical orlistat weight loss results If you take Alli with a high-fat meal Young people aged years vol 1 Sample Participants who had been prescribed orlistat by the GP and registered on the Xenical support system MAP funded by Roche were invited to take part in the study and sent the baseline questionnaire Brown urine How does Alli work?