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I.V. TEMAZEPAM: THEORETICAL AND CLINICAL CONSIDERATIONS

HALLIDAY, N. J.; DUNDEE, J. W.; CARLISLE, R. J. T.; MCCLEAN, E.
BJA: British Journal of Anaesthesia , Volume 59 (4): 465 Oxford University PressApr 1, 1987

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I.V. TEMAZEPAM: THEORETICAL AND CLINICAL CONSIDERATIONS

Abstract

Abstract Two injectable forms of temazepam, in 90% propylene glycol or 40% salicylic acid, were studied in volunteers, and before surgery in healthy patients. The volunteers also received two forms (capsule and elixir) by mouth. The salicylate preparation was painful on injection and both i.v. formulations caused an unaccep-tably high incidence of venous thrombosis. Temazepam was detected in plasma earlier following the elixir preparation than the capsule. Plasma concentrations were similar following both injectable preparations. The potency of i.v. temazepam in inducing drowsiness in patients was much less than expected and doses greater than 0.6 mg kg −1 were required to produce adequate sedation. There was a significant reduction in thiopentone induction dose in patients receiving temazepam i.v. © 1987 British Journal of Anaesthesia
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/lp/oxford-university-press/i-v-temazepam-theoretical-and-clinical-considerations-3Bu1PjC6Kf
Title
I.V. TEMAZEPAM: THEORETICAL AND CLINICAL CONSIDERATIONS
Author(s)
HALLIDAY, N. J.; DUNDEE, J. W.; CARLISLE, R. J. T.; MCCLEAN, E.
Journal
BJA: British Journal of Anaesthesia , Volume 59 (4): 465 Oxford University Press – Apr 1, 1987
Publisher
Oxford University Press
Copyright
Copyright © 1987 Oxford University Press
ISSN
0007-0912
eISSN
1471-6771
D.O.I.
10.1093/bja/59.4.465
Publisher site
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