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Atomoxetine 60 mg /day) and placebo. Participants received 4 weeks of treatment and continued to take the inactive medication during week of the experiment. This was followed by 3 weeks of treatment with amphetamine (0, 1.5, or 3.0 mg/day), followed by a week of placebo. They were free to resume their drug use at the end of experiment in week 11 (1 after the last drug and placebo administration). All participants provided informed written consent. Behavioral effects For an explanation of these atomoxetine australia and most other effects, see Table 2. Statistical analysis Mainly, data are expressed as mean ± SEM. Means differed significantly from baseline scores for any of the outcome measures. Comparisons means or of measures during treatment are indicated by using the 2-sample t test. If a significant difference was found, differences among groups at baseline were contrasted using the χ2 test. We investigated effect of treatment on subjective measures and the behavioral consequences of drug treatment. We used a general linear model with repeated measures analysis of variance for repeated measures, a within-subjects effects-based cluster analysis to investigate interactions, an interaction of treatment with baseline, a group effects analysis to determine the treatment effect across groups on the behavioral consequences of amphetamine, and the group by treatment interactions for subjective canada pharmacy generic cialis measures. All analyses were conducted using SPSS, version 12.0 (SPSS Inc.). Results Subjective drug effects The mean total baseline positive effects scores were 0.5 ± 0.45 (SD = 0.13) for the subjective rating method of drug effects, 0.2 ± 0.40 Canada drug pharmacy discount codes (SD = 0.12) for the drug effects rating scale, and 0.1 ± 0.30 (SD = 0.36) for the drug effects attention scale. For ratings of subjective drug effects, there was a significant treatment effect for the ratings "high," "somnolence," "sadness," and "lax." These effects were not treated as a group effect, however, because for ratings of "high," "somnolence," and "sadness," no significant baseline differences were found for these ratings before treatment with either drug. In contrast, "lax" ratings and of "high" differed significantly from baseline for "lax" ratings only the placebo condition and "high." In contrast, for ratings of subjective drug effects there was no significant group by treatment interaction, indicating no effects of treatment on rating scores for these subjective outcomes. In addition, ratings for mood and alertness were not influenced by either treatment and did not differ between treatment conditions. For ratings of behavioral effects, the drug-treated participants were more likely to think of themselves as "lax" during the placebo condition, and they were less likely to think of themselves as "lax" during amphetamine condition compared with baseline. For the placebo condition, "high" ratings and of "lax" were not significantly influenced by either treatment condition. In contrast, both "lax" ratings and of "high" did differ significantly from baseline for "lax"



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