ITEM 6
ADVICE TO
THE EXPERT ADVISORY COMMITTEE ON DRUGS
ON:
FURTHER ADVICE ON PIPERAZINES
AN UPDATE ON EVENTS POST FEBRUARY 2004
NOVEMBER 2006
link to page 2 link to page 2
Executive Summary
This paper presents an overview of recent research findings and significant media
events since the Ministry of Health previously provided advice to the EACD on
benzylpiperazine (BZP) in February 2004. Available research results are included and
an outline is provided for projects due to report to the Committee before the next
meeting takes place. Also included are the details of significant media events, as well
as petitions and submissions that the Ministry of Health has received regarding the
controls upon, and legal status of BZP.
Background
BZP was considered by the Committee in April 2004. It was concluded that, based on
the criteria that the EACD must apply before making a recommendation to the Minister,
there was insufficient information available on which to base a recommendation to
classify this substances in the Misuse of Drugs Act 1975. The Commit ee considered
that “more information on the health effects of BZP and similar substances should be
obtained,” and the prevalence of BZP use should be investigated.
The Commit ee further considered BZP in June 2005 and noted that the quantity of the
substance imported had increased from a 3 year average of 400kgs to approximately
1100kgs and that doses of BZP contained in ‘party pil s’ had in some products
increased to 750mgs. Members also agreed that a priority for BZP research should be
to focus on the level of uncertainty around effects of long term, or chronic use, and also
to gauge an understanding of the prevalence of polydrug use with BZP and alcohol
and/or other drugs.
Substance Identification
Piperazines are stimulant type substances that form the main active ingredients present
in almost all ‘party pil s’, and are also available for purchase as a raw powder. In the
last 5 years New Zealand has witnessed growth in the industry, both in the quantity of
products being consumed and in the number of manufacturers of ‘party pil s’ entering
the market. The EACD has previously given advice on BZP, the base ingredient found
in the majority of ‘party pil s,’ and also considered the significance of
triflurophenylmethylpiperazine (TFMPP) in this context. The industry has recently
moved to also include the piperazine p-fluorophenylpiperazine (PFPP) in selected party
pil product
s1
and 1-(meta-chlorophenyl)piperazine (MCPP) and 1-(4-
methoxyphenyl)piperazine (meOPP) may also be currently used for recreation
purposes.
2
1
http://www.funkpil s.com/index.php?act=viewProd&productId=50
2 www.wackyherbs.com
link to page 3
Current Classification
BZP is a ‘Restricted Substance’ as specified in the Misuse of Drugs Amendment Act
2005. As such the sale of products containing BZP are confined to those over 18 years
of age and restrictions have been placed on the nature in which products containing
BZP may be advertised or distributed. Other piperazines including TFMPP and PFPP
have not been placed in either controlled or restricted drug schedules and therefore are
subject only to industry self-regulation.
Research
Massey University (SHORE)
Earlier this year the Centre for Social and Health Outcomes Research and Evaluation
(SHORE) at Massey University published a report titled “Legal party pil use in New
Zealand: Prevalence of use, availability, health harms and ‘gateway effects’ of
Benzylpiperazine (BZP) and Triflurophenylmethylpiperazine (TFMPP).” The study
conducted a random sample of 2,010 people aged between 13-45 years. Findings that
may be of interest to the Committee are:
•
20% of the sample had ever tried legal party pil s and 15% of the sample had
used legal party pil s in the last year. Of this last year use, nearly half of the
sample had only consumed party pil s 1-2 times in this period.
•
One user (0.6% of the sample) reported they typically injected their party pil s
•
The mean number of party pil s taken on a typical occasion was 2.6 pil s;
10.9% of the sample had taken 8 or more pil s at one time.
•
32% of the sample stated that they ‘drink more alcohol’ than normal when
using legal party pil s.
•
The physical problems most commonly experienced by users from legal party
pil s use were ‘insomnia,’ ‘poor appetite’, ‘hot/cold flushes’, ‘heavy sweating,’
‘stomach pains/nausea’ and ‘headaches.’ 4 users reported ‘fainting/passing
out’ and 1 user reported having ‘fits/seizures’.
•
Psychological problems most commonly reported by users were ‘strange
thoughts,’ ‘mood swings,’ ‘confusion’ and ‘irritability’.
•
Of the sample that consumed party pil s in the last year, 2.2% could be
classified as dependent upon them by scoring greater than 4 on the Short
Dependency Scale, a measure that had previously been validated for
detecting amphetamine dependency.
3
University of Auckland (School of Pharmacy)
A second study funded by the National Drug Policy Discretionary Fund has been
conducted by Sheridan and Butler (2006) and is titled “Legal party pil s and their use by
3 Wilkins et al (2006) Legal party pil use in New Zealand: Prevalence of use, availability, health harms
and ‘gateway effects’ of benzylpiperazine (BZP) and triflourophenylmethylpiperazine (TFMPP).
link to page 4
young people”. This study employed a qualitative research design and obtained results
from both young people aged 16-24 years, and also key informants including
representatives from alcohol and other drug services, health services, education, youth
organisations, health promotion, the legal party pil industry, event organisation and
national drug organisations.
4 The Secretariat has obtained a recent draft report of the
study. Key results include:
•
BZP use, as well as being linked to the ‘dance party’ culture for the purpose
of ‘staying power’ and ‘increased socialization’, is also being consumed for
‘functional means’ such as for studying assistance and weight loss.
•
The same similarities in use patterns of MDMA (ecstasy) are being found with
BZP, including the use of other substances to manage the ‘comedown’ period
and also negative effects such as ‘mood fluctuations’ and ‘depression’ in the
period after taking the drug.
•
Young people appear to be engaging in risky behaviors with regard to legal
party pil use. Examples include: mixing substances, driving whilst under the
influence and taking larger doses than recommended. However, the study
found limited evidence of significant harms being experienced as a result of
such activities.
•
Young people were generally aware that certain behaviors could lead to
increased risk with taking legal party pil s and were considered to be well
informed in regard to harm reduction messages such as not mixing BZP with
alcohol.
•
Young people were more likely to seek advice from their friends rather than
consulting packaging or leaflets for information on safe use, appropriate
dosage, etc.
•
Given the ‘inferior high’ and unpleasant comedown, legal party pil s were not
generally considered a viable substitute for ecstasy amongst ecstasy users.
The authors have agreed that a final version of this study wil be made available for
consideration by the EACD.
National Poisons Centre
The National Poisons Centre at the University of Otago are in the final stages of
compiling research into cases of poisoning due to piperazine-based party drugs (PBPD)
in New Zealand. The results, which are expected to be made available to the EACD,
wil provide information on:
• Specific toxicology knowledge of PBPD, their effects, toxic doses and medical
management of poisoning.
4 Sheridan, J and Butler, R., (2006) Legal party pil s and their use by young people.
School of Pharmacy,
The University of Auckland.
link to page 5
• Recommendations on the safety of PBPD to relevant groups such as the
Ministry of Health, health professionals, and the general public.
• Advice to the public on the issue of PBPD poisoning, including prevention
education.
University of Auckland (Dr Bruce Russell)
A further study is taking place at Auckland University to investigate the effects that both
BZP and TFMPP, either in combination or alone, have on memory and neurological
function. This study wil be the first controlled trial to investigate the effects of TFMPP
and wil also extend the limited literature available on BZP.
It is expected that a report detailing preliminary results wil be made available for
consideration by the EACD.
Medical Research Institute of New Zealand
This study conducted by the Medical Research Institute of New Zealand (MRINZ) aimed
to investigate the effect of BZP, either alone or in combination with alcohol, on driving
performance. An interim safety analysis was undertaken after 35 subjects had
completed the investigative models and due to concerns about the frequency, nature,
and severity of the side effects that participants had reported, a decision was made to
halt the study. 41% of participants in the BZP/TFMPP group (with or without alcohol)
suffered an adverse event following use of the piperazines. No severe events were
reported in the placebo, or alcohol only groups. Examples of adverse events reported
include:
•
Severe agitation, anxiety
•
Severe headache, fatigue
•
Severe anxiety, panic attack (required medical treatment)
•
Hallucinations, agitation & anxiety
•
Severe vomiting, confusion
•
Severe migraine (‘worst ever’)
5
The authors of the study have indicated that a revised report on the safety effects of
party pil s containing BZP and TFMPP wil be made available for consideration by the
EACD.
Ministry of Health Pill Testing.
The primary rationale for this research was to pharmaceutically test a number of legal
party pil s for consistency in levels of piperazines between doses of a given product. A
5 Thompson et al (Unpublished report) (2006) The safety effects of party pil s containing Benzylpiperazine
(BZP) and Trifluoromethylpiperazine (TFMPP) with and without alcohol.
link to page 6 link to page 6
secondary aim was to identify what, if any piperazines other than BZP and TFMPP are
now being included in legal party pil s. The need for this testing has come from the
realisation that certain internet sites
6 are distributing the piperazines 1-(meta-
chlorophenyl)piperazine (MCPP), 1-(4-methoxyphenyl)piperazine (meOPP) and p-
fluorophenylpiperazine (PFPP) along side BZP and TFMPP for recreational use. The
products to be tested were identified by studies from SHORE, the University of
Auckland and the Ministry’s knowledge base and represent the products most
commonly reported as being used by participants from each of the seven major
manufacturers.
A second round of testing is currently being proposed to the target the party pil s in
which the effects claimed are not consistent with traditional use of BZP and/or TFMPP,
and which may contain comparatively high quantities of active ingredients. The Ministry
has also received allegations that some products may potentially contain controlled drug
analogues. The Ministry wil consult with ESR on this, and include these products in
future tests if appropriate.
The results from the first round of this testing, which is being undertaken by the
Pharmaceutical Division of ESR wil be available for consideration by the EACD at the
upcoming meeting.
Medical cases
Dr Paul Gee (Christchurch Hospital)
A report has been published by Gee et al (2005) titled “Toxic effects of BZP-based
herbal party pil s humans: a prospective study in Christchurch, New Zealand”. The
study documented all presentations associated with piperazine use between 1 April and
1 September 2005 and reported: “A total of 61 patients presented on 80 occasions to
the Emergency Department of Christchurch Hospital and patients that had an adverse
reaction had taken an average of 4.5 tablets/capsules. Patients with mild to moderate
toxicity were classified as experiencing symptoms such as insomnia, anxiety, nausea,
vomiting, palpitations, dystonia and urinary retention. Some adverse reactions persisted
up to 24 hours after ingestion and 15 toxic seizures were recorded with 2 patients
suffering life-threatening toxicity”. This study concludes by stating that BZP “can have a
narrow safety margin” and may cause “unpredictable and serious toxicity in some
individuals”.
7
6
www.wackyherbs.com
7 Gee, P. Richardson, S. Woltersdorf, W and Moore, G., (2005) Toxic effects of BZP-based herbal party
pil s in humans a prospective study in Christchurch, New Zealand.
The New Zealand Medical Journal,
118
link to page 7
Dr Mohammed Alansari (Waikato Hospital)
Alansari and Hamilton (2006) have published a report investigating the nephrotoxicity of
BZP. The study investigates the case of a 17 year old male who consumed 5 BZP-
based party pil s and a small amount of alcohol. A few hours after ingestion the subject
developed bilateral loin pain that worsened over the next 24 hours. 36 hours after
ingestion he was admitted to hospital and then later transferred to a specialised renal
unit. The subject was discharged in due course and his kidney function returned to
baseline levels after 3 weeks. The authors conclude that “the acute renal failure
observed here may be related to a direct toxic effect of the party pil s on the kidneys”.
8
Petitions
On 23 March 2006 Jacqui Dean, MP and 7,500 others presented a petition requesting
that
• “Parliament review the classification of Party Pils with that review encompassing
the health, psychological, social and community safety impacts of these
substances.”
On 13 September 2006 Roy Ramsey from Drug Arm (Blenheim) Youth Workers Forum
and 3,600 others presented a petition requesting that:
• “Parliament legislates banning the use, manufacture and sale of party pil s due to
the negative health, psychological, and social impacts of these substances upon
our community’s safety.”
The Ministry of Health has provided reports to the Health Select Committee on the
above two petitions and the Clerk of the Committee has indicated that the Committee
wil consider both petitions in tandem early in 2007.
Submissions
Subsequent to the petition presented by Jacqui Dean, the Member has also provided
the EACD with a submission expressing her concerns over the way in which party pil s
are affecting New Zealand. The Secretariat notes that the EACD is considering this
submission as an agenda item.
Media Events
BZP has continued to receive attention in the media with coverage now extending to
international agencies. Examples of some recent media stories are attached as
appendices to this report.
8 Alansari, M and Hamilton, D., (2006) Nephrotoxicity of BZP-based herbal party pil s: a New Zealand
case report.
The New Zealand Medical Journal, 119
References
Alansari, M and Hamilton, D., (2006) Nephrotoxicity of BZP-based herbal party pil s: a
New Zealand case report.
The New Zealand Medical Journal, 119
Gee, P. Richardson, S. Woltersdorf, W and Moore, G., (2005) Toxic effects of BZP-
based herbal party pil s in humans a prospective study in Christchurch, New Zealand.
The New Zealand Medical Journal, 118
http://www.funkpil s.com/index.php?act=viewProd&productId=50
Sheridan, J and Butler, R., (2006) Legal party pil s and their use by young people.
School of Pharmacy, The University of Auckland.
Thompson et al (Unpublished report) (2006) The safety effects of party pil s containing
Benzylpiperazine (BZP) and Trifluoromethylpiperazine (TFMPP) with and without
alcohol.
Wilkins et al (2006) Legal party pil use in New Zealand: Prevalence of use, availability,
health harms and ‘gateway effects’ of benzylpiperazine (BZP) and
triflourophenylmethylpiperazine (TFMPP).
Centre for Social Outcomes Research and
Evaluation. Massey University.
Appendix one
Pil casualties down 50%
27 September 2006
By ANNA CLARIDGE
The number of party-pil users going to Christchurch Hospital's emergency department has halved in the
past year.
Doctors are seeing just two patients a week, compared with a high of six a week at this time last year, and the
number arriving with seizures and blackouts has also dropped.
Emergency medicine specialist Dr Paul Gee said that while numbers were down, the department was stil seeing
patients as young as 14 with overdose symptoms.
In one case, a two-year-old had consumed his mother's supply of party pil s.
"I think (the numbers have dropped) because people realise that it can be dangerous and are using it a bit more
cautiously," Gee said.
"Also, most people who want to try, have, and as (the Massey University) study shows, more than half don't like the
experience and wil stop.
"In fact, most who use are of the opinion that BZP should be banned."
Party pil s, marketed as herbal but containing the drug benzylpiperazine (BZP), leave many users feeling agitated,
dehydrated and strung out.
The pil s caught the headlines two years ago after several overdoses prompted medical professionals to speak out.
The drug is banned in the United States.
Gee said the fal in the number of Christchurch patients may be a reflection that the herbal-high craze has passed.
His comments are backed by a study released this year by Massey University's Centre for Social and Health
Outcomes Research and Evaluation that showed one in five young people had tried the pil s and 50 per cent said
they would not try them again.
The Government last year created a class D classification for BZP-based pills and restricted their sale to people aged
over 18, but Gee said this was not behind the drop in patient numbers.
The Government had commissioned three studies into the pil s, and Associate Health Minister Jim Anderton said he
would not make a decision on whether to ban them until the results were in.
Mairead Harnett, a researcher with the National Poisons Centre in Dunedin, said staff were just finishing a study of
the known BZP poisoning cases treated at hospitals in the past three years. "We are focusing on dose, symptoms
and the medical management," Harnett said.
"Our ultimate aim is to be able to provide more accurate and comprehensive poisoning management advice to the
public and hospitals."
Over a two-year period, the centre had about 180 cal s and at least 120 suspected cases of poisoning.
Appendix Two
Medics advise total avoidance of party pil s
10.30am Wednesday November 1, 2006
Party pil s containing the ingredient Benzylpiperazine (BZP) can cause seizures, paranoia and hypothermia, and
people should stay away from them altogether, the New Zealand Medical Association says.
People with a history of psychiatric il ness in particular should avoid taking the pil s, which should not be mixed with
alcohol, other drugs or prescription medicines.
The legal status of pil s containing BZP, originally developed as a drug to treat cattle with worms, is under question,
and the association recommended in a statement today that people should not take them until their status is
determined.
NZMA chairman Ross Boswell said there were growing concerns about the safety of BZP-based party pills.
A recent study at Christchurch Hospital had examined 61 patients, presenting 80 times to the emergency department.
Patients with adverse effects had taken an average of 4.5 tablets or capsules and suffered symptoms including
insomnia, anxiety, nausea, vomiting, palpitations, and muscle spasms.
Fifteen toxic seizures were recorded and two patients suffered life-threatening conditions.
Dr Boswell said if people did take the pil s they should make sure they stuck to the manufacturer's recommended
dose of one or two pil s, and not combine them with other stimulants.
While the pil s were often marketed as "herbal", there was nothing herbal about them, he said.
Further research on the effects of BZP is soon to be released by the Health Minister, Dr Boswell said.
NZPA
Appendix Three
Legal high: the party pil s stronger than ecstasy
The selection of legal, mind-altering drugs, similar to cocaine, ecstasy and speed, are being legal y sold over the
counter to anyone aged over 18, in at least 13 so-called ‘head stores’ around the country, as well as stal s outside big
music festivals and gigs.
Support groups are becoming increasingly concerned about the recent explosion of pep pil s because they contain
the dangerous substance benzylpiperazine (BZP) which acts as a substitute for MDMA, the banned substance in
ecstasy and speed pil s.
Despite warnings from experts that they cause heart problems and panic attacks, the Government said it has no
plans to ban them. However, it is backing a new drugs awareness campaign being launched to warn young people of
the dangers of these “legal highs”.
The Department of Health said BZP is not a scheduled substance under the Misuse of Drugs Act, but its status is
kept under constant review. However, it is banned and classified as a Class A substance in the US since 2002.
In a statement, the Department of Health said it “reviews any evidence that substances are being abused and are
causing significant harm to public health. For example, earlier this year the law surrounding pyscho- tropic
mushrooms in their raw state was clarified in the light of evidence of increased availability and significant harm being
done”.
The National Advisory Commit ee on Drugs (NACD) discussed the emerging trend for the first time at a meeting two
weeks ago. It said it wil gather information on BZP and consult with its EU counterparts before making any
recommendations to the Government.
Support groups say Jax pil s and Smileys — both containing BZP and five times the strength of any other dance pil s
— are becoming the drug of choice for col ege-goers and even Leaving Cert students, who see them as a more
accessible and safer alternative to drugs such as speed, Ecstasy and LSD.
Dr Des Corrigan from the Trinity College School of Pharmacy, said BZP is no safer than any other drug. “The main
concern would be dehydration and the risk of heat stroke. The other concerns would be head- aches and a flu like
hangover that lasts a few days. There is also the risk of panic reactions and high blood pressure. It would surprise me
if anyone would think they are getting anything safer,” Dr Corrigan said.
Michael McDonagh of the Drugs Awareness Programme (DAP) said caffeine and herbal tablets have been around for
a long time, but since May they are getting more and more calls about these pil s, which are a bit more serious in
what they contain.
“We are concerned that they wil become a big story at exam time next year,” Mr McDonagh said.
DAP and the Health Service Executive (HSE) are planning an awareness campaign for early next year, which wil
advise young people, their parents, and professionals about the dangers of these drugs.
DAP said since the ban on magic mushrooms earlier this year it has received thousands of calls relating to Salvia, a
more dangerous but legal hallucinogen.
DAP is calling for the regulation of the socalled ‘head stores’ which sel these pil s, along with growing kits, pipes and
other accessories.
Appendix Four
David Braithwaite
October 10, 2006 - 4:18PM
The online purchase of a New Zealand-made drug touted as the "strongest energy pil legal y available in the world"
could land NSW residents in jail, police have warned.
The benzylpiperazine-based products are legal in New Zealand and marketed online under names such as "Dark
Angel", "Grin", "Red Hearts", "Majik", "Kandi", "Frenzy", "Altitude" and "Humma", police said.
Paul Dil on, information manager at the National Drug and Alcohol Research Centre in Sydney said the drug was a
stimulant.
"It basically gives you a buzz," he said.
New Zealand had created a new classification of drug to cover benzylpiperazine-based products, he said.
"Some are like amphetamine and some are like ecstasy, in a milder form," he said.
Research into the drugs, along with lobbying to legalise them, was driven by NZ entrepeneur Matt Bowden, because
he was concerned about the rise in methamphetamine, or "speed", use in NZ.
Mr Dil on said the problem was, like with al drugs, they could be harmful and some people were taking more of them
to get a high.
NSW residents in possession of the synthetically produced drugs faced two years' jail, the commander of the Drug
Squad, Detective Superintendent David Laidlaw, said.
"We have identified a number of New Zealand-based companies advertising on the internet, which are supplying
residents across Australia with these products," he said.
"Law enforcement agencies in both countries are liaising with the companies to make management aware of the
legalities of providing a drug of this type to NSW residents.
"While these companies have not broken laws in New Zealand, NSW residents receiving packages of tablets
containing benzylpiperazine face prosecution and possible jail time."
Smh.com.au was able to find three New Zealand-based websites selling benzylpiperazine-based pil s online within
minutes.
One pil , called "Bolts", was "like a lightning bolt of pure energy straight to your brain", a website said.
"Bolts are guaranteed to make your jaws clench, your hair stand on end and your feet want to hit the dance floor.
"Bolts are the strongest energy pil s legally available in the world today."
The site included usage instructions for the pil s, such as "do not redrop for at least two hours", and noted they were
not "herbal highs" but "semisynthetic legal highs".
The pil s could not be shipped to Australia, Sweden, Greece or the US, the website said, warning buyers they should
check with their local customs department before ordering.
But another website, for an Auckland-based sports nutrition store, did not mention any restriction on the sale
of benzylpiperazine-based pills to Australia.
The website sells a two-pack of "Majik" pil s, described as "great for more experienced users wanting a strongly
altered perception" for $NZ20 ($17.70).
Police said benzylpiperazine was a synthetic drug developed as a potential antiparasitic agent and listed as a
prohibited drug in NSW.
Superintendent Laidlaw said benzylpiperazine could produce an increased heart rate, nausea, headaches, fatigue,
insomnia, seizures, confusion and mild memory loss.
Police said at least one death has been officially linked with the use of benzylpiperazine.
"We are concerned that NSW residents ordering these tablets via the internet are unaware of it being il egal to
possess," Superintendent Laidlaw said.
"People are also jeopardising their lives by using these tablets and we strongly warn residents against purchasing or
using them."
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