Ország: Egyesült Királyság
Nyelv: angol
Forrás: MHRA (Medicines & Healthcare Products Regulatory Agency)
Adenosine
Wockhardt UK Ltd
C01EB10
Adenosine
3mg/1ml
Solution for injection
Intravenous
No Controlled Drug Status
Valid as a prescribable product
BNF: 02030200; GTIN: 5012727907376
OBJECT 1 ADENOSINE 3MG/ML SOLUTION FOR INJECTION Summary of Product Characteristics Updated 15-Jun-2015 | Wockhardt UK Ltd 1. Name of the medicinal product Adenosine 3mg/ml Solution for Injection 2. Qualitative and quantitative composition Each vial contains 6mg of adenosine per 2ml (3mg/ml). Contains sodium. For a full list of excipients, see Section 6.1. 3. Pharmaceutical form Solution for injection (injection). A clear, colourless solution free from visible particles. 4. Clinical particulars 4.1 Therapeutic indications Rapid conversion to a normal sinus rhythm of paroxysmal supraventricular tachycardias, including those associated with accessory by-pass tracts (Wolff-Parkinson-White Syndrome). _Paediatric population_ Rapid conversion to a normal sinus rhythm of paroxysmal supraventricular tachycardia in children aged 0 to 18 years. DIAGNOSTIC INDICATIONS Aid to diagnosis of broad or narrow complex supraventricular tachycardias. Although adenosine injection will not convert atrial flutter, atrial fibrillation or ventricular tachycardia to sinus rhythm, the slowing of AV conduction helps diagnosis of atrial activity. Sensitisation of intra-cavitary electrophysiological investigations. 4.2 Posology and method of administration METHOD OF ADMINISTRATION Adenosine should be administered by rapid intravenous (IV) bolus injection into a vein or into an IV line. If given into an IV line it should be injected through as proximally as possible, and followed by a rapid saline flush. If administered through a peripheral vein, a large bore cannula should be used. During administration of adenosine cardio-respiratory resuscitation equipment must be available for immediate use if necessary. Adenosine is intended for use with continuous monitoring and ECG recording during administration. Patients who develop high-level AV block at a particular dose should not be given further dosage increments. POSOLOGY ADULTS: Initial dose: 3mg given as a rapid intravenous bolus (over 2 seconds). Second dose: If the first dose does not result Olvassa el a teljes dokumentumot