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Additional resources for A nonparametric procedure associated with a clinically meaningful efficacy measure (2000)(en)(6s)
London: Wellcome Historical Medical Library, 1966. Wax PM. History. In: Goldfrank’s Toxicologic Emergencies, 6th edn. Goldfrank LR, Flomenbaum NE, Lewin NA, Weisman RS, Howland MA, Hoffman RS (eds). Stamford, CT: Appleton & Lange, 1998: 1–18. Wilson IB, Ginsburg S. A powerful reactivator of alkylphosphate-inhibited acetylcholinesterase. Biochim Biophys Acta 1955; 18: 168–70. Witthaus RA. Manual of Toxicology. New York: Wood, 1911. Wolff RS, Wirtschafter D, Adkinson C. Ocular quinine toxicity treated with hyperbaric oxygen.
4). 5). Nowadays the pure opioid antagonist naloxone is used in treating patients acutely poisoned with opioids and related compounds such as pentazocine. A further opioid antagonist, diprenorphine, is used widely in veterinary medicine because it has a longer half-life than naloxone in many animal species. 5: Nalorphine 3 mg reversing respiratory depression caused by 50 mg pethidine in a patient lightly anaesthetized with cyclopropane. 2). v. theophylline (aminophylline). , 1984). 13) have rendered theophylline treatment of benzodiazepine poisoning obsolete.
The patient eventually made a full recovery (Hort, 1834). Meanwhile, the absorptive properties of charcoal of animal origin were being exploited as a chemical reagent (Rand, 1848). Graham and Hofman (1853) in London, for example, used ivory-black or animal charcoal as a means of extracting strychnine from beer. However, [Sir] Alfred Baring Garrod (1819–1907), working at Aldersgate Medical School in London, performed the first controlled studies of purified animal charcoal in the treatment of poisoning (Garrod, 1846).