Medicines Safety Update
- Aust Prescr 2014;37:168-71
- 4 August 2014
Medicines Safety Update is the medicines safety bulletin of the Therapeutic Goods Administration (TGA)
In this issue
Measles, mumps, rubella, varicella (MMRV) vaccine is a combination live virus vaccine for immunisation against these four common childhood illnesses.
While MMRV vaccine is approved for use in children from nine months of age, on 1 July 2013 it was added to the National Immunisation Program (NIP) schedule to be given at 18 months after an initial dose of measles, mumps, rubella (MMR) vaccine at 12 months of age.
Like most vaccines, MMRV vaccine can cause some mild adverse events. In rare cases, fever after vaccination can lead to febrile convulsions in young children.
MMRV vaccine is only recommended for use as a second dose of measles-containing vaccine. This is because MMRV vaccine administered as a first dose in children aged 9–30 months is associated with an increased rate of fever and febrile convulsions, compared to separate MMR and varicella vaccination.
As described in the postmarketing data section of the Product Information (PI), the attributable risk of febrile convulsions 5–12 days following MMRV vaccination as a first dose of measles-containing vaccine is 3.64/10 000 (95% CI: –6.11;8.30). This equates to one additional case of febrile convulsion per 2747 young children, when compared to MMR or concomitant MMR and varicella vaccination.
When used as the second measles-containing vaccination, there is no indication of an increased risk.
The overall risk of fever and subsequent febrile convulsion in children is greatly reduced by following the NIP schedule of the initial dose of MMR vaccine at 12 months and the second vaccine dose, as MMRV, at 18 months.
Dosage instructions in the PI recommend an interval of six weeks to three months between the first and second vaccine doses. As with other live virus vaccines, under no circumstances should the interval be less than four weeks.
Further information for health professionals is available on the Immunise Australia website.
The TGA continues to receive adverse event reports that suggest MMRV vaccine has been administered as the first dose of measles-containing vaccine in children aged 12 months or younger. In the 12 months to 1 May 2014, the TGA received seven such reports. There were also two reports of MMRV vaccine being given at the same time as other vaccines that contain either MMR or varicella.
Adverse events following immunisation at any age should be reported through the usual reporting mechanisms in your State or Territory or to the TGA.
Fentanyl is an opioid analgesic, interacting predominantly with mu-opioid receptors. Various strengths of fentanyl transdermal delivery system products (patches) are funded under the Pharmaceutical Benefits Scheme as a restricted benefit for 'chronic severe disabling pain not responding to non-narcotic analgesics'.
Like other opioids, at lower doses fentanyl may cause constipation, nausea and vomiting, hypotension, dysphoria and euphoria, urinary retention, blurred vision, impaired cognition and sedation. As the dose increases, it can also cause:
Non-users who are opiate naïve, and especially children, are at greater risk of very serious adverse events if they are inadvertently exposed to or ingest fentanyl patches, whether they be used or unused.
The Product Information (PI) for fentanyl patches includes instructions to keep the products out of reach of children before, during and after use, as well as other precautionary information. The PI also provides instructions for the safe disposal of patches.
The opiate dose delivered through fentanyl patches is high, with 12 microgram considered approximately equivalent to 45 mg per day of oral morphine. Even used patches can retain high residual levels of the active ingredient (about 60% of the intended dose).1
To 1 May 2014, the TGA has received two reports involving fentanyl patches and accidental exposure in children.
The children in these two cases suffered somnolence and loss of consciousness respectively. Both of the children were hospitalised as a result of the incidents.
The TGA is also aware of reports made to the NSW Poisons Information Centre involving accidental exposure to fentanyl patches in children aged younger than five years.
In 2012, the US Food and Drug Administration evaluated a series of 26 cases of accidental exposures to fentanyl patches in children reported over a 15-year period. Of those 26 cases, 10 resulted in death and 12 in hospitalisation. Sixteen of the 26 cases occurred in children two years old or younger. 2
Ensure patients are aware of the risks of accidental exposure to fentanyl patches for non-users and in particular children.
Advise patients to keep fentanyl patches out of reach of children before, during and after use, and to appropriately dispose of patches that have been used or are no longer needed. Specifically, used patches should be folded so that the adhesive side adheres to itself, before being wrapped and disposed of carefully. Unused patches should be returned to the pharmacy for safe disposal.
Fentanyl patches being worn by patients can come into contact with non-users in situations of close contact, and there have been recorded cases of patches being transferred to another person while sharing a bed with a patch wearer.
If a fentanyl patch adheres to a non-user, it should be removed immediately. Advise patients to contact a doctor immediately in any case of suspected exposure to or ingestion of fentanyl patches.
Toxicological advice is available from the Poisons Information Centre's 24-hour phone line on 131 126.
Zolpidem (Stilnox) is an imidazopyridine with relative selectivity for the type 1 benzodiazepine receptor subtype. It has been registered in Australia for the short-term treatment of insomnia in adults since 1999.
Currently marketed presentations for Stilnox and Stilnox CR are:
There are also generic brands of zolpidem 5 mg and 10 mg marketed in Australia. The Product Information (PI) for zolpidem includes a precaution regarding the drug's effect on the patient's ability to drive and use machinery. It warns that patients should not drive or operate machinery for eight hours after taking the drug and that drowsiness may continue the following day.
The PI also includes a black box warning that, among other things, advises health professionals to use caution when this drug is used with other central nervous system (CNS) depressant drugs.
The Product Information documents for prescription-only diclofenac have been updated to provide further information about the increased risk of arteriothrombotic events.
Diclofenac is a non-steroidal anti-inflammatory drug (NSAID). Prescription-only products are available in oral and rectal forms.
Information regarding arteriothrombotic events was previously included in the precaution and adverse reaction sections of the Product Information (PI). However, the updated PI includes details from meta-analyses of individual participant data from randomised trials by the Coxib and traditional NSAID Trialists' Collaboration that estimated, in comparison with placebo, use of diclofenac caused about three additional major vascular events per 1000 patients per year. This information was derived from trials involving long-term (more than 28 days) treatment with high-dose diclofenac (150 mg/day).1
You should discuss with patients the benefits and risks associated with this drug before prescribing it. Educate patients regarding the signs and symptoms of arteriothrombotic events.
To minimise risks, the lowest effective daily dose should be used for the shortest duration necessary to control symptoms. Patients with cardiovascular disease or other risk factors may be at greater risk. The TGA is undertaking a review of all NSAIDs with regard to their association with cardiovascular risks.
What to report? You don't need to be certain, just suspicious!
The TGA encourages the reporting of all suspected adverse reactions to medicines, including vaccines, over-the-counter medicines, herbal, traditional or alternative remedies. We particularly request reports of:
Reports may be submitted:
For more information about reporting, visit www.tga.gov.au or contact the TGA's Office of Product Review on 1800 044 114.
Medicines Safety Update is aimed at health professionals. It is intended to provide practical information to health professionals on medicine safety, including emerging safety issues. The information in Medicines Safety Update is necessarily general and is not intended to be a substitute for a health professional's judgment in each case, taking into account the individual circumstances of their patients. Reasonable care has been taken to ensure that the information is accurate and complete at the time of publication. The Australian Government gives no warranty that the information in this document is accurate or complete, and shall not be liable for any loss whatsoever due to negligence or otherwise arising from the use of or reliance on this document. © Commonwealth of Australia 2016. This work is copyright. You may reproduce the whole or part of this work in unaltered form for your own personal use or, if you are part of an organisation, for internal use within your organisation, but only if you or your organisation do not use the reproduction for any commercial purpose and retain this copyright notice and all disclaimer notices as part of that reproduction. Apart from rights to use as permitted by the Copyright Act 1968 or allowed by this copyright notice, all other rights are reserved and you are not allowed to reproduce the whole or any part of this work in any way (electronic or otherwise) without first being given specific written permission from the Commonwealth to do so. Requests and inquiries concerning reproduction and rights are to be sent to the TGA Copyright Officer, Therapeutic Goods Administration, PO Box 100, Woden ACT 2606 or [email protected]