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Prescribing limits

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:

  • Prescribing within scope of practice (Regulation 39 and 39A): medical practitioners, dentists and midwives are now able to prescribe any prescription medicines that fall within their scope of practice. Midwives will no longer be restricted to prescribing only for antenatal, intrapartum, and post-natal care periods. They will still only be allowed to prescribe for patients under their care. All prescribers must only prescribe within their scope of practice for patients under their care.
  • Period of supply of dentists’ prescriptions (Regulation 39A): removal of the 10 day limit of dentists prescribing. This means that dentists (and other authorised prescribers) can prescribe a maximum of three months supply of a prescription medicine.
  • Period of supply in special circumstances (Regulation 39A): the Director-General of Health is now able to authorise an extension of the period of supply of a prescription medicine in certain circumstances.
  • Limit on period of supply of prescription medicines.

(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.

Privileged Statement Under Section 98 of the Medicines Act

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

Suspension of Avandia (rosiglitazone) from New Zealand market

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

DHB Summary of Serious and Sentinel Events 2010

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.

Pandemic Influenza Mortality and Morbidity Review Group

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).

Fatal Accidents and Sudden Deaths (Scotland) Act 1976

Posted 15 Oct 2010

DETERMINATION of SHERIFF LINDA MARGARET RUXTON in FATAL ACCIDENT INQUIRY into the death of GORDON EWING

Withdrawal of Reductil

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 1Interview 2 .

Hyperbaric bupivacaine

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?

Equipment failure

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.

Wayne Pneumothorax Drainage Set Recall

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.

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