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Topamax 50 mg 60 film tablet (Teva Pharmaceuticals, Indianapolis, IN) in the morning, and a 12-h fasting period on the day of study. Subjects were instructed to eat a normal balanced diet and to abstain from alcohol before and at the beginning of study. study was approved by the Human Subjects Committee at Indiana University. After a minimum 2-wk washout period, participants were randomized to either the lorazepam group (n = 9) or the placebo group (n = 8). The placebo group was administered with matching lorazepam tablets, and the group received matching capsules containing identical capsules. The study was conducted between May and August, 1988. Subjects were excluded if they had a history of seizures, substance abuse or dependence, psychiatric disorders (including mood disorders), or had taken any other medications that could influence the effects of psychotropic medication or drugs during the previous 3 d before study. Patients who failed to comply with the study rules or who were found to be using prescription stimulant medication within 3 d before the study, had blood drawn at this time, and had negative results on drug screens were excluded from the present study. Before enrollment, a medical history was obtained in which the participant was given a comprehensive examination by physician knowledgeable in the use of psychotropic medications. Subjects were excluded if they had any history of seizures, a mood disorder, or had used prescription stimulant medication during the previous 3 d before study. The participant was asked to read the information sheet on use and safety of psychotropic medications, any questions were answered verbatim. Subjects then screened by a psychopharmacologist who rated the intensity to effects of psychotropic medications and determined compliance with the study rules. If all of the questions had been answered correctly, the participant was then enrolled in the study. This screening buy topamax weight loss was repeated at least 3 weeks before the beginning of each treatment period. The participants were asked to write a 3-page statement describing any symptoms they thought might have, if any. During the day of testing (morning at 7:15 AM, noon, and 2:00 PM) these patients also completed a questionnaire (see below). After enrollment, all study subjects completed a series of questionnaires topamax weight loss for sale before each study period. The Brief Psychiatric Rating Scale has been used in the past examination of antidepressant pharmacologic effects in subjects with psychiatric disorders cost of topamax australia and has been used as a tool for the assessment of drug compliance with pharmacologic treatment.4 Since the drug-comparison groups for this study were identical, only the data from these subjects were used in this report. The Brief Psychiatric Rating Scale (BDS) consists of 20 adjectives, each rating up to a maximum score of 100. Each question uses an adjectival response, such as "not at all," "moderately," "extremely," "extremely unpleasant," and "very difficult to describe." For each item, the adjectives are presented as numerical answers which range from "0" (no response) to 100 (exactly 100). The ratings range from 0 (very unpleasant) to 100 pleasant), with being the highest possible response. scale can range from 3 to 14 points; a score of less than 2 indicates excellent adherence to the medication and a score of 3 means that patients could be considered as highly compliant. The BCS was given to each patient who tested positive for the presence of an antidepressant medication. This was done with the help of a laboratory technician who was not a familiar person of the patient.

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