Krajina: Arménsko
Jazyk: angličtina
Zdroj: Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում
atracurium (atracurium besylate)
Swiss Parenterals Pvt. Ltd.
atracurium (atracurium besylate)
10mg/ml
solution for injection
Prescription
PRODUCT NAME: ATRACURIUM BESYLATE INJECTION 10 MG/ML, 2.5 ML DOSAGE FORM: SOLUTION FOR INJECTION _ _ _ _ _Confidential _ 1. SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF THE MEDICINAL PRODUCT Atracurium Besylate Injection 10 mg/ml, 2.5 ml 2. QUALITATIVE AND QUANTITATIVE COMPOSITION QUALITATIVE DECLARATION Atracurium Besylate Injection 10 mg/ml, 2.5 ml QUANTITATIVE DECLARATION Each ml contains: Atracurium Besylate 10 mg Water for Injections q.s. DESCRIPTION Atracurium Besylate Injection is clear, colourless solution filled in a glass ampoule. Atracurium besylate is designated as Isoquinolinium, 2,2-[1,5- pentanediylbis[oxy(3-oxo-3,1-propanediyl)]]bis[1-[(3,4-imethoxyphenyl)methyl]- 1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-, dibenzenesulfonate. - INN Name is Atracurium Besylate. PHARMACOLOGIC CLASSIFICATION: Nondepolarizing neuromuscular blocker THERAPEUTIC CLASSIFICATION: Skeletal muscle relaxant 3. PHARMACEUTICAL FORM Sterile Solution for Injection PRODUCT NAME: ATRACURIUM BESYLATE INJECTION 10 MG/ML, 2.5 ML DOSAGE FORM: SOLUTION FOR INJECTION _ _ _ _ _Confidential _ 4. CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Atracurium Besylate Injection is a highly selective, competitive or non-depolarising neuromuscular blocking agent, which is used as an adjunct to general anaesthesia to enable tracheal intubation to be performed and to relax skeletal muscles during surgery or controlled ventilation. 4.2 POSOLOGY AND METHOD OF ADMINISTRATION INJECTION: Atracurium Besylate Injection is administered by intravenous injection. The dosage range for adults is 0.3 to 0.6 mg/kg (depending on the duration of full block required) and will provide adequate relaxation for 15 to 35 minutes. Endotracheal intubation can usually be accomplished within 90 seconds from the intravenous injection of 0.5 to 0.6 mg/kg. Full block can be prolonged with supplementary doses of 0.1 to 0.2 mg/kg as required. Successive supplementary dosing does not give rise to accumulation of neuromuscular blocking effect. CONTINUOUS INFUSION: NORMOTHERMIA: Prečítajte si celý dokument