Central House, 26 Brandon Street | Wellington | PO Box 10691
T. 04 494 0124 F. 04 494 0125 E. nzsa@anaesthesia.org.nz
Central House, 26 Brandon Street | Wellington | PO Box 10691
T. 04 494 0124 F. 04 494 0125 E. nzsa@anaesthesia.org.nz
Amendments to the Medicines Regulations 1984 and the Medicines (Standing Order) Regulations 2002 were announced early in 2011. A number of changes took effect on 1 August, with the remainder effective from 1 December. More
The changes, effective from 1 December, include:
(1) An authorised prescriber may not on any occasion prescribe for any patient a quantity of any prescription medicine that exceeds—
(a) 6 months' supply in the case of an oral contraceptive; or
(b) 3 months' supply in any other case.
(2) However, the Director-General may, at his or her discretion, authorise—
(a) an authorised prescriber to prescribe for any patient, or any specified class or classes of patients, a quantity of a prescription medicine exceeding the period of supply in subclause (1)(a) or (b):
(b) a class of authorised prescribers to prescribe for any patient, or any specified class or classes of patients, a quantity of a prescription medicine exceeding the period of supply in subclause (1)(a) or (b).
Regulation 39A: inserted, on 1 December 2011, by regulation 15 of the Medicines Amendment Regulations 2011 (SR 2011/245).
The Medicines Amendment Regulations 2011, the Medicines (Standing Order) Amendment Regulations 2011 and other related legislation are available online at www.legislation.govt.nz.
Director-General of Health Kevin Woods today warned retailers to remove from their shelves a brand of herbal smoking product called Kronic Pineapple Express because it contains a prescription medicine. More
Diabetes medicine rosiglitazone will be withdrawn from the New Zealand market on 29 April 2011 after a safety review found an elevated risk of cardiovascular events in patients treated with this...More
The Health Quality & Safety Commission has released the 2009/2010 report of serious and sentinel events reported by the country's District Health Boards on17 November 2010.
This group, set up in November last year to provide clinical review of deaths associated with pandemic influenza A (H1N1) during its first wave and independent advice on clinical and prevention strategies ahead of the second wave in 2010, released its report on 15 October 2010. During 2009, a total of 119 patients were admitted to intensive care units, and 1122 people were admitted to hospitals with a primary diagnosis of pandemic influenza A (H1N1) 2009. Eighty-six percent of the 49 people who died during 2009 had co-morbidities (underlying medical conditions) and other risk factors. The most common were respiratory disease, obesity and substance abuse (including alcohol abuse).
DETERMINATION of SHERIFF LINDA MARGARET RUXTON in FATAL ACCIDENT INQUIRY into the death of GORDON EWING
Posted 14 Oct 2010
Following preliminary results of a major study of 10,000 patients that sibutramine raises the risk of heart attacks and strokes, the ministerial advisory committee MARC (the Medicines Adverse Reactions Committee which makes recommendations on appropriate action to be taken on medicine safety issues), has, in conjunction with Medsafe, confirmed that the risks outweigh the benefits of using the prescription weight-loss drug sibutramine. The medicine has since been withdrawn by pharmaceutical company Abbott. Sibutramine, which is sold under the brand name Reductil in New Zealand, was also withdrawn from sale in Australia, Canada and the United States recently and is estimated to have been used by 5000-6000 New Zealanders. Interview 1. Interview 2 .
Posted 25 Aug 2010
Problems have been reported with the efficacy of heavy bupivacaine 0.5% spinal from AstraZeneca. Despite easy access to the subarachnoid space and free flow of CSF, blocks have been slow in onset with inadequate sensory block requiring repeat spinal, or epidural top-up or physical manipulation (head down manoeuvres) to obtain adequate blocks for surgery. So far all events have been with one batch of heavy bupivacaine 0.5%. This is batch number BMC2926 expiry date 03-2013. Other batches have been fine. This is not the same batch that gave problems in Rotorua earlier in the year.
Posted 27 May 2010
It has been noted that one hospital has had a cluster of failed spinal anaesthetics. A common factor has been the batch of Asta-Zeneca’s hyperbaric bupivacaine (number LH2843). NZSA has informed Medsafe of the issue. Could any departments having a similar problem please notify the Society?
Posted May 2010
GE and FDA Class I Recall of specific lots of the Aisys and Avance Anesthesia Systems. The control board wiring harnesses have a defect which can cause the machine to unexpectedly shut down, terminating ventilation, anesthetic delivery, and potentially patient monitoring. For advice view the FDA site here.
Posted 19 Mar 2010
The Therapeutic Goods Administration (TGA), Australian Department of Health and Ageing, has been notified of several incidents involving the Wayne Pneumothorax drainage set supplied to hospitals by Cook Australia Pty Ltd.