The Therapeutic Goods Administration (TGA) has announced that it will proceed with international harmonisation of drug names used in Australia from April 2016. For the past decade or so, since the United Kingdom moved to the World Health Organization’s International Nonproprietary Names (INNs), we’ve been in the anomalous situation of using former British Approved Names despite these no longer being used in the UK (nor listed in the British Pharmacopoeia). The TGA website has a list of affected drugs.
Some changes are trivial:
- Substitution of “ph” with “f” (e.g. cefalexin, guaifenesin)
- Substitution of “y” with “i” (e.g. amoxicillin, ciclosporin)
- Substitution of “th” with “t” (e.g. indometacin)
Others are more significant (and will require dual-labelling for 3 years), for example:
- Dosulepin (dothiepin)
- Formoterol (eformoterol)
- Furosemide (frusemide)
- Glycopyrronium bromide (glycopyrrolate)
- Hydroxycarbamide (hydroxyurea)
- Lidocaine (lignocaine)
On the contentious subject of adrenaline vs epinephrine, the TGA has followed the UK practice where dual-labelling “adrenaline (epinephrine)” will be used indefinitely.
Estimated glomerular filtration rate (eGFR) and creatinine clearance (CrCl) are often, incorrectly, used interchangeably when discussing renal function and drug dose adjustment.
Creatinine clearance, usually estimated using the 1976 Cockcroft-Gault formula rather than actually measured by (notoriously unreliable) 24-hour urine collection, has traditionally been used for drug dosing as it is relatively standardised despite overestimating renal function due to tubular secretion of creatinine. In addition to the usual caveats associated with basing renal function estimates on serum creatinine (acute illness, muscle mass, diet, etc), accuracy of the formula is limited by changes to serum creatinine assays and the rise in obesity since 1976.
Renal function is assessed nowadays using formula-derived eGFR (actual GFR is impracticable to measure routintely). Until recently this was usually calculated using the MDRD formula (1999), which has been well validated but has limited accuracy above 60 mL/min. Laboratories in Australia now report eGFR calculated using the superior CKD-EPI formula (2009). Although both of these formulae give better estimates of true renal function (GFR) than CrCl, they are both still based on serum creatinine with its associated caveats above.
Some studies have shown a reasonable concordance between CrCl (Cockcroft-Gault) and eGFR (MDRD) with respect to drug dosing,1 whereas others have noted significant differences.2–3 At the end of the day, CrCl and eGFR are not the same thing and prescribers should remain vigilant as to which measurement has been used to formulate dosage adjustment recommendations.
1. Stevens LA, et al. Am J Kidney Dis 2009;54:3342
2. Wargo KA, et al. Ann Pharmacother 2006;40:124853
3. Park EJ, et al. Ann Pharmacother 2012;46:117487
Whilst giving a presentation at grand rounds recently, I noted that approved names for biological medications in Australia are suffixed with a three-letter abbreviation – the “biotechnology descriptor” – to indicate the biotechnology production system used, e.g. insulin lispro (rbe).
The most common biotechnology descriptors are:
- ghu – gene-activated human cell line
- rbe – recombinant bacteria Escherichia coli
- rch – recombinant Chinese Hamster ovary cell line
- rmc – recombinant mouse cell line
- rys – recombinant yeast Saccharomyces cerevisiae
Incidentally, I cringe whenever someone refers to this group of medications as “biologics” – an Americanism that has crept into the Australian medical lexicon. Australian English still retains the “-ical” ending (rather than shortening to “-ic” in American English), therefore we should continue to refer to these medications as “biologicals”.
Ballots closed recently for the Pharmacy Council of New South Wales 2013 election. Voting as a registered pharmacist in NSW, I was only familiar with a few of the candidates and so had to rely on the Candidate Information Sheet that was sent out. I’ve reproduced page 4 below (de-identified)…
The nomination paperwork clearly indicated that the “candidate information” section would be reproduced exactly as submitted… The candidate at the top of the page did not get elected.
I was asked to take the official photo for the National Australian Pharmacy Students’ Association (NAPSA) Congress 2008, this year hosted by the Sydney University Pharmacy Association (SUPA) – both organisations with which I have had a fair bit of involvement over the years.
NAPSA Congress Sydney 2008 official congress photo
(click on image for full-size version)
To achieve this image, I borrowed a Canon EF-S 10–22mm f/3.5–4.5 USM ultrawide zoom lens from a friend and performed a perspective correction during post-processing in Adobe Photoshop. A commercial Fujifilm Frontier Digital Minilab was used to prepare 30 cm x 20 cm prints, which were distributed to congress delegates.
It was also a great honour to have had the opportunity on the day to meet Her Excellency Professor Marie Bashir, Governor of New South Wales and Chancellor of the University of Sydney. As an adolescent psychiatrist, Professor Bashir is highly regarded amongst medical students at Sydney Medical School and I found, during our conversation, that her reputation is indeed very much deserved.
Update (10 Feb 2008): Full-size NAPSA Congress Sydney 2008 photo now available for download.
It seems that most of us in the Sydney Medical School have become suckers for mnemonics… Recently, after the Problem 4.05 theme session on drugs in pregnancy, I came up with a mnemonic to help people remember the Australian Drug Evaluation Committee (ADEC) pregnancy categories used for medications in Australia.
- Category A = A-OK – generally considered safe
Drugs which have been taken by a large number of pregnant women and women of childbearing age without any proven increase in the frequency of malformations or other direct or indirect harmful effects on the fetus having been observed. (ADEC, 2007)
- Category C = Careful – may be harmful
Drugs which, owing to their pharmacological effects, have caused or may be suspected of causing, harmful effects on the human fetus or neonate without causing malformations. These effects may be reversible. Accompanying texts should be consulted for further details. (ADEC, 2007)
- Categories B = Buggered if I know – limited data available
Drugs which have been taken by only a limited number of pregnant women and women of childbearing age, without an increase in the frequency of malformation or other direct or indirect harmful effects on the human fetus having been observed. (The allocation of a B category does NOT imply greater safety than the C category.) (ADEC, 2007)
- Category D = Danger – risk of irreversible harm
Drugs which have caused, are suspected to have caused or may be expected to cause, an increased incidence of human fetal malformations or irreversible damage. These drugs may also have adverse pharmacological effects. Accompanying texts should be consulted for further details. (ADEC, 2007)
- Category X = X-men – high-risk teratogens
Drugs which have such a high risk of causing permanent damage to the fetus that they should not be used in pregnancy or when there is a possibility of pregnancy. (ADEC, 2007)
Of course the use of drugs in pregnancy requires more than simply looking-up the ADEC pregnancy category, but the categorisation does prove quite useful as a quick reference in clinical practice.