The average range of a drop in the ventricular rate after the drug use was 46 ± 18 times per minute in Group I and 30 ± 12 times per minute in Group H (P < 0.05).
Transient intraocular pressure elevation occurred in one patient (6.25%) of all the 16 eyes and intraocular pressure returned to the normal after a transient treatment with antiglaucoma medication.
The development of sleep medication, computer technologies, and microelectronics in the past decade brought about the creation of a new class of instruments for the diagnostics of sleep disorders, i.e., computerized polysomnographic systems.
The effect of medication (Nakom, Cyclodol, and Bromocriptine for 3-6 months) on the electromyogram (EMG) parameters of muscular fatigue and recovery after exercise was studied in patients with Parkinson's disease (PD).
In the patients on medication, tolerance to exercise increased approximately twofold and the maximum strength during fatigue and recovery was lower than before medication.
The pharmacokinetics of α- and β-diastereomers of Arteether, a well-known antimalarial drug and its active metabolite dihydroartemisinin (DHA) were studied in Sprague-Dawley rats, Rhesus monkeys and human volunteers.
The prevalence and pattern of psychotropic drug use was investigated in an urban walk-in clinic in Nigeria during the course of a two-stage epidemiological survey.
A gene regulatory mechanism has been proposed in which steroid hormones and certain other drugs bind to nuclear receptor proteins followed by transfer to DNA where they are inserted between base pairs.
Here, we report using the estrogen receptor that the location of drugs in x-ray crystal structures of the receptors matches closely their predicted spatial locations in the DNA.