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1.
Clin Ther ; 22(10): 1151-68; discussion 1149-50, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11110228

ABSTRACT

OBJECTIVE: This article reviews the pharmacology, pharmacokinetics, clinical efficacy, adverse effects, drug interactions, and dosing of rosiglitazone, the second thiazolidinedione approved for the treatment of type 2 diabetes mellitus. METHODS: Background information for this article was obtained from searches of MEDLINE , Iowa Drug Information Service, and International Pharmaceutical Abstracts, as well as from data on file with the manufacturer of rosiglitazone. RESULTS: Rosiglitazone is indicated for use alone or in combination with metformin or sulfonylureas for the maintenance of glycemic control in patients with type 2 diabetes mellitus. Rather than stimulation of insulin secretion, rosiglitazone's primary mechanism of action is sensitization of tissues to insulin through activation of the peroxisome proliferator-activated receptor gamma and increasing expression of the glucose transporter-4 receptor. Rosiglitazone is administered orally, is absorbed almost completely, and is 99.8% bound to plasma proteins. The majority of a dose is metabolized by the cytochrome P-450 2C8 isozyme, with the inactive metabolites excreted primarily in the urine. Four to 8 mg/d of rosiglitazone given alone or in combination with metformin, sulfonylureas, or insulin has produced reductions in baseline fasting plasma glucose and glycosylated hemoglobin in studies of up to 1 year's duration. Common adverse effects (occurring in > or = 5.0% of patients) include upper respiratory tract infection, injury, and headache. Edema, weight gain, and increased low-density lipoprotein cholesterol concentrations have also been observed. It is recommended that rosiglitazone be avoided in patients with alanine aminotransferase levels >2.5 times normal. No clinically relevant drug interactions have been documented with rosiglitazone to date. The initial starting daily dose of rosiglitazone is 4 mg in single or divided doses, without regard to meals, to a maximum of 8 mg. CONCLUSIONS: No direct comparative trials of the efficacy and safety of rosiglitazone versus those of the other available thiazolidinedione, pioglitazone, have yet been performed. The role of rosiglitazone as a single agent and in combination with other antidiabetic agents remains to be clarified as additional comparative and long-term data become available.


Subject(s)
Diabetes Mellitus, Type 2/drug therapy , Hypoglycemic Agents , Thiazoles , Thiazolidinediones , Aged , Area Under Curve , Biological Availability , Clinical Trials as Topic , Drug Interactions , Drug Therapy, Combination , Humans , Hypoglycemic Agents/adverse effects , Hypoglycemic Agents/blood , Hypoglycemic Agents/pharmacokinetics , Hypoglycemic Agents/therapeutic use , Insulin/therapeutic use , Metformin/therapeutic use , Middle Aged , Rosiglitazone , Thiazoles/adverse effects , Thiazoles/blood , Thiazoles/pharmacokinetics , Thiazoles/therapeutic use
2.
J Forensic Sci ; 33(3): 826-8, 1988 May.
Article in English | MEDLINE | ID: mdl-3385389

ABSTRACT

A 16-year-old boy was riding his bicycle when he was struck by a truck. He was dragged over 2 1/2 miles (4 km) before he was deposited on the side of the road. The injuries evident at autopsy revealed the boy died from dragging and not from the initial impact. The scene, and the autopsy findings, will be discussed.


Subject(s)
Accidents, Traffic , Bicycling , Sports , Wounds and Injuries/pathology , Adolescent , Autopsy , Humans , Male
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