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psychomotor, and physiological effects of tramadol in recreational drug users by Zacny JP. Department of Anesthesia and Critical Care, University of Chicago, 5841 S. Maryland Avenue, Chicago, IL 60637, USA. Drug Alcohol Depend. 2005 Jul 5 ABSTRACT Tramadol is a mu opioid agonist that also inhibits the reuptake of norepinephrine and serotonin. Because non-medical use of prescription opioids, including tramadol, has increased in the U.S. over the last several years, we sought to profile its subjective, psychomotor, and physiological effects in recreational drug users. Twenty-two subjects received placebo, 50 or 100mg tramadol, morphine, or 2mg lorazepam in a randomized, crossover, double-blind design. The last 12 subjects in the study received 25mg morphine, a dose that is putatively equianalgesic to 100mg tramadol. In these subjects, morphine induced miosis and several other mu agonist subjective effects; 100mg tramadol increased "feel drug effect" and drug liking ratings, and decrease 100mg tramadol


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D pupil size, but the miotic effect was not statistically significant. Lorazepam, but neither tramadol nor morphine, impaired psychomotor performance. When the placebo, tramadol, and lorazepam data from all 22 subjects were analyzed, 100mg tramadol induced miosis, and several subjective effects were increased significantly, including ratings of drug liking and "want to take again." The present results indicating that a clinically-prescribed dose of oral tramadol has abuse liability-related effects in recreational drug users suggest the need for further abuse liability testing of the oral formulation in opioid abusers. Children Tramadol (Ultram) Tramadol: dosage Tramadol and analgesia Tramadol and acute pain Tramadol and osteoarthritis Tramadol as an antidepressant Discriminative stimulus effects Tramadol: risk benefit analysis Tramadol versus buprenorphine Tramadol, morphine and the mouse Refs HOME HedWeb BLTC Research Utopian Surgery? The Hedonistic Imperative MDMA: Utopian Pharmacolo

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100mg tramadol Many; K. Junge, Department of Biostatistics, ASTA Medica AG, Frankfurt, Germany; H. Momberger, Galenical Department, Temmler Pharma GmbH, Marburg, Germany; D. Kuhn, Medical Department, Temmler Pharma GmbH, Marburg, GermanyAbstract and IntroductionAbstractObjective: To investigate the analgesic efficacy, tolerability and therapeutic equivalence of a newly developed tramadol sustained-release (SR) capsule compared with a tramadol immediate-release (IR) capsule in patients with moderate to severe chronic low back pain.Design: Randomised, multicentre, double-blind, parallel-group study.Setting: Patients were provided with a diary card into which they recorded by use of a visual analogue scale (VAS) the intensity of pain immediately before every intake of study medication during the 9 treatment days. Besides pain intensity, secondary efficacy parameters included a sleep questionnaire, a functional capacity score and the patient's global assessment of efficacy.Patients: 247 patients of eithe

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