Држава: Нови Зеланд
Језик: Енглески
Извор: Medsafe (Medicines Safety Authority)
Adrenaline 1mg;
Pharmacy Retailing (NZ) Ltd t/a Healthcare Logistics
Adrenaline 1 mg
1mg/10mL
Solution for injection
Active: Adrenaline 1mg Excipient: Hydrochloric acid Sodium chloride Sodium hydroxide Sodium metabisulfite Tartaric acid Water for injection
Ampoule, glass, Type I coloured, 10mL, 10 dose units
Restricted
Restricted
Boehringer Ingelheim Pharma GmbH & Co KG
Adrenaline 1:10,000. An adjunct in the management of cardiac arrest.
Package - Contents - Shelf Life: Ampoule, glass, Type I coloured, 10mL - 10 dose units - 18 months from date of manufacture stored at or below 25°C
2011-01-05
ASPEN ADRENALINE Injection CMI - 230310 Page 1 of 3 ASPEN ADRENALINE INJECTION _adrenaline acid tartrate _ CONSUMER MEDICINE INFORMATION (CMI) WHAT IS IN THIS LEAFLET This leaflet answers some common questions about ASPEN ADRENALINE Injection. It does not contain all the available information. It does not take the place of talking to your doctor or pharmacist. All medicines have risks and benefits. Your doctor has weighed the risks of you being given ASPEN ADRENALINE Injection against the benefits they expect it will have for you. IF YOU HAVE ANY CONCERNS ABOUT BEING GIVEN THIS MEDICINE, ASK YOUR DOCTOR OR PHARMACIST. KEEP THIS LEAFLET._ _ You may need to read it again. WHAT ASPEN ADRENALINE INJECTION IS USED FOR ASPEN ADRENALINE Injection is usually only given in cases of extreme emergency. ASPEN ADRENALINE is used in the emergency treatment of severe allergic reactions to insect bites or stings, medicines, foods or other substances. It may also be given during acute asthma attacks for severe breathing difficulties. ASPEN ADRENALINE opens up the airways making it easier to breathe. ASK YOUR DOCTOR IF YOU HAVE ANY QUESTIONS ABOUT WHY THIS MEDICINE HAS BEEN PRESCRIBED FOR YOU. Your doctor may have prescribed it for another reason. This medicine is not addictive. It is available only with a doctor’s prescription. This medicine is not expected to affect your ability to drive a car or operate machinery. BEFORE YOU ARE GIVEN IT _WHEN YOU MUST NOT BE GIVEN IT _ YOU MUST NOT BE GIVEN ASPEN ADRENALINE INJECTION IF YOU HAVE AN ALLERGY TO: • any medicine containing adrenaline • any of the ingredients listed at the end of this leaflet. S Прочитајте комплетан документ
1 NEW ZEALAND DATA SHEET 1. ASPEN ADRENALINE INJECTION 1MG/ML AND 1MG/10ML 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Adrenaline acid tartrate equivalent to adrenaline 1:1,000 (1mg/mL) and adrenaline 1:10,000 (1mg/10mL) Adrenaline is a white or creamy-white, odourless, crystalline powder or granule. It darkens in colour on exposure to air and light. The BP solubilities are: practically insoluble in water, in ethanol (96 %) and in methylene chloride. It dissolves in hydrochloric acid. For a full list of excipients, see section 6.1. 3. PHARMACEUTICAL FORM Solution for injection. ASPEN ADRENALINE Injection should be used only once and any residue discarded. It should not be used if it is coloured. 4. CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS ADRENALINE 1:1,000. The drug of choice in the emergency treatment of acute severe anaphylactic reactions due to insect bites, drugs and other allergens. It may also be used for the symptomatic relief of respiratory distress due to bronchospasm. ADRENALINE 1:10,000. An adjunct in the management of cardiac arrest. 4.2 DOSE AND METHOD OF ADMINISTRATION ASPEN ADRENALINE 1:1,000 injection is preferably administered subcutaneously. It may also be administered intramuscularly but not into the buttocks. In emergency situations, adrenaline may be injected very slowly intravenously but only as the dilute solution 1:10,000. ASPEN ADRENALINE Injection is for single use in one patient only. Discard any residue. Adrenaline injection should not be used if it is coloured. CARDIAC ARREST. ADULTS. The recommended dose is 1 mg intravenously, using 10 mL of the 1:10,000 solution. This may be repeated every three to five minutes. If given through a peripheral line, each dose should be followed by a flush of 20 mL of intravenous fluid to ensure delivery of the drug to the central compartment. Intracardiac administration is no longer recommended. CHILDREN. The recommended dose is 10 microgram (0.1 mL of the 1:10,000 solution)/kg bodyweight administered intravenously. This may be repeated every Прочитајте комплетан документ