Lorazepam is a short-acting and rapidly cleared benzodiazepine used commonly as a sedative and anxiolytic. It was developed by DJ Richards, presented and marketed initially by Wyeth Pharmaceuticals in the USA in 1977. The first historic FDA label approval is reported in 1985 by the company Mutual Pharm.
Lorazepam is FDA-approved for the short-term relief of anxiety symptoms related to anxiety disorders and anxiety associated with depressive symptoms such as anxiety-associated insomnia. It is as well used as an anesthesia premedication in adults to relieve anxiety or to produce sedation/amnesia and for the treatment of status epilepticus.
Some off-label indications of lorazepam include rapid tranquilization of an agitated patient, alcohol withdrawal delirium, alcohol withdrawal syndrome, muscle spasms, insomnia, panic disorder, delirium, chemotherapy-associated anticipatory nausea and vomiting, and psychogenic catatonia.
CHRISTUS Santa Rosa Children's Hospital, San Antonio, Texas, United States
Arnold Palmer Hospital for Children, Orlando, Florida, United States
Vanderbilt-Ingram Cancer Center, Nashville, Tennessee, United States
GSK Investigational Site, La Jolla, California, United States
GSK Investigational Site, Barcelona, Spain
Queen Elizabeth Central Hospital, Paediatric Dept, Box 360, Blantyre, Malawi
Virginia Commonwealth University Medical Center, Richmond, Virginia, United States
Medical University of South Carolina - Center for Drug and Alcohol Programs, Charleston, South Carolina, United States
GSK Investigational Site, Zwolle, Netherlands
German Research Network on Schizophrenia, Department of Psychiatry and Psychotherapy at the Heinrich-Heine-University Düsseldorf, Düsseldorf, North Rhine-Westphalia, Germany
UCLA, Los Angeles, California, United States
Paediatric Emergency Department, Queen Elizabeth Central Hospital, Blantyre, Malawi
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