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Current issues and challenges in New Zealand

Globally, treatment and knowledge about migraine have improved in recent years. Sadly, New Zealand has been left behind

The number and variety of treatments for migraine have expanded greatly in past years. People with migraine no longer have to take medications that were developed for other diseases; there are now treatments specifically targeted at migraine.

These include medications to treat or abort migraine attacks when they occur (abortive treatments), medications to prevent attacks from happening (preventive treatments) and devices that may abort or prevent attacks.

For medicines and devices to be available in New Zealand, they must be approved by Medsafe, the agency responsible for assessing the safety and efficacy of all medical products. Once approved by Medsafe, a product may be considered for funding by Pharmac, the agency responsible for deciding which products are subsidised for use in the community and in hospitals. Products that have been approved by Medsafe but are not funded by Pharmac may be purchased at the full price.

Access to triptans

Triptans are abortive medications that can be taken by mouth, nasal spray or injection to treat a migraine attack. They were the first abortive medications developed specifically for migraine.


There are currently seven triptans available globally to treat a migraine attack, including five short-acting, one medium-acting and one long-acting. This gives people a range of options to help abort a migraine attack, as different triptans may be more or less effective for an individual, or have different side effects.

But in New Zealand

Only two triptans are funded and available in New Zealand. Both are short-acting. If neither of these medications are effective, there are no other migraine-specific abortive medications available for people in New Zealand to try.

In March 2022, after languishing on Pharmac’s application list for nearly 10 years, additional triptans including frovatriptan, naratriptan and zolmitriptan were declined for Pharmac funding.

Access and funding for Calcitonin Gene-Related Peptide (CGRP) monoclonal antibody medications

Calcitonin gene-related peptide (CGRP) monoclonal antibodies are the first medications developed specifically to prevent migraine. They have been found to be safe and effective, with fewer side effects than many other preventive migraine medications. They are taken by injection.

The CGRP monoclonal antibodies block a small protein called CGRP that helps to transmit pain signals in the brain, ramp up inflammation and dilate blood vessels. The CGRP monoclonal antibodies bind to CGRP or to its receptor sites found in some parts of the nervous system, effectively turning off its ability to stimulate the cascade of events that lead to a migraine attack.


Since May 2018, the US Food and Drug Administration (FDA) has approved three injectable CGRP medications and one CGRP infusion:

  • Aimovig (erenumab)
  • Emgality (galcanezumab)
  • Ajovy (fremanezumab)
  • Vyepti (eptinezumab)

Aimovig, Emgality and Ajovy are given once a month by self-injection. Ajovy also has the option to use quarterly, with three injections four times a year. Vyepti is a one-hour intravenous infusion every three months.

In Australia, Emgality and Ajovy have been approved on the Pharmaceutical Benefits Scheme (PBS, similar to Pharmac in New Zealand), which means people in Australia now have funded access to both. Aimovig and Vyepti are available privately. In the UK, Aimovig, Emgality and Ajovy are available through the National Health Service for people with migraine who have failed three other preventive treatments.

But in New Zealand


Medsafe has approved Aimovig and it is available as a 70mg and 140mg dose. It’s available on prescription, but it’s not funded and a 70mg injection costs $678 and 140mg costs $1,356.


Medsafe has approved Emgality and it is available as a 120mg dose (cost may vary, from $325). Two injections (240mg) are given initially, then one every 4 weeks. Your GP can prescribe Emgality for you – it doesn't require a neurologist prescription. Your GP may want to find out more information about it if they're not familiar with prescribing it, because it only became available in New Zealand in September 2022.

Emgality should be available through any chemist in New Zealand. The wholesaler is CDC Pharmaceuticals, but even pharmacies that don't usually purchase medicine from CDC can still get Emgality through them. Prices may vary, but Grafton Pharmacy is Auckland is offering it at $325 per dose, plus a courier fee.

Please visit our Emgality Advocacy Toolkit to learn more about advocating for funding in New Zealand, and our Emgality Frequently Asked Questions.


Medsafe has approved Ajovy but it is not yet available in New Zealand.


Vyepti has yet to be approved by Medsafe.

Access and funding for gepants and ditans

Gepants and ditans are new oral migraine abortive medications that have been specifically developed to treat migraine. Ditans are similar to triptans but unlike triptans, ditans do not constrict blood vessels and may be used by people with heart or blood vessel diseases.

Gepants are a type of calcitonin gene-related peptide (CGRP) inhibitor used to treat migraine attacks. Gepants can help people who cannot take or tolerate triptans or for whom triptans don’t work. Gepants are also being considered for use as a preventive migraine medication.

Currently, three gepants and one ditan are on the market and more are in development:

  • Ubrogepant (Ubrelvy)
  • Rimegepant (Nurtec ODT)
  • Atogepant (Qulipta)
  • Lasmiditan (Reyvow)


As of 2022, gepant and ditan medications are available in the USA.

But in New Zealand

Gepants and ditans are currently not available in New Zealand.

Funding for Botox injections to prevent migraine

Botox (onabotulinumtoxinA) injections have been found to reduce headache frequency and severity in people with chronic migraine (at least 15 headache days a month).


In 2010, the US Food and Drug Administration (FDA, similar to Medsafe in New Zealand) approved the use of Botox in people with chronic migraine.

Botox is funded for the prevention of headaches in people with chronic migraine in many other countries including Australia, the UK and parts of Canada.

But in New Zealand

Pharmac agreed to fund Botox for use in public hospitals in 2017 for a range of conditions, not just chronic migraine. However, most public hospitals have chosen not to fund Botox for people with chronic migraine, or have restricted access, so that most people in New Zealand cannot access funded Botox. Self-funded Botox costs approximately $1,200 per session, and requires one session every 12 weeks.

Access to neuromodulator devices

Neuromodulation uses non-invasive electrical currents or magnetic pulses to change the activity of the nerve pathways in the brain. Neuromodulation can help to turn down brain activity involved in migraine pain and decrease the frequency of migraine attacks.

Different types of neuromodulator devices work in various ways, including stimulation of specific nerves (e.g. the trigeminal nerve in the face, the vagus nerve in the neck, or the occipital nerve in the back of the head) or more general stimulation of the brain. Most neuromodulator devices can be used as both acute and preventive treatment.


Overseas there are a range of neuromodulator devices available, such as CEFALY, Relivion, GammaCore Sapphire and Nerivio, which can be used at home to help prevent a migraine attack or during a migraine. More invasive nerve stimulation options are also available.

But in New Zealand

Mynd Migraine Relief, a transcutaneous electrical nerve stimulator (TENS)  neuromodulator, was available through a New Zealand supplier until December 2021. Since then, people in New Zealand have had difficulty accessing it without a New Zealand contact.

Qalm, by PainGone, is a similar TENS device that is available in New Zealand and is recognised by MedSafe. You can order Qalm through the website: and use the code MIGRAINEFANZ to receive 20% off. For every Qalm purchased using this discount code, Migraine Foundation Aotearoa New Zealand receives a small donation.

Qalm is also available at various New Zealand retailers (information on the PainGone website).

Awareness and knowledge about migraine disease

Many people don’t understand what migraine disease is, how it can be treated and how it affects people. For example, many people are unaware that migraine is a hereditary condition that often runs through families.

Common myths about migraine disease include that migraine is a women’s problem, eliminating certain foods from your diet can minimise migraine attacks or headache medication will cure migraine. However, many men also get migraine, diet is complicated (for example, craving chocolate and cheese are often part of the early stage of a migraine attack, rather than causing it; caffeine can help treat a migraine attack, but caffeine withdrawal can trigger one) and there is no cure for migraine, despite what some people claim – although it can be managed successfully.

The most common myth, that migraine is ‘just a headache’, can lead to misunderstandings about the severity and impact of migraine disease. The effects of a migraine attack can last for hours to days beyond the headache stage, and other symptoms of a migraine attack can be as debilitating as the headache, including nausea and vomiting, visual disturbances, light and sound sensitivity, brain fog, speech difficulties, fatigue and mood changes.

It’s not only the general public who don’t have a good understanding of migraine disease. Health professionals may not know how to distinguish migraine from other headache conditions, or be aware of the best management options. Dr Katy Munro, a headache specialist GP in the UK says, “Many doctors lack training in migraine diagnosis and treatment” and Dr Tissa Wijeratne, a neurologist in Australia, says that, “migraine is … the least respected and worst managed medical disorder worldwide”.

Without a broad and widespread understanding about migraine disease among society, health professionals, employers, educators and others, people with migraine in New Zealand can struggle to get diagnosed, and get the treatment and support they need to manage migraine in the best possible way.

Access to specialist services

People with migraine in Aotearoa New Zealand often face difficulties in accessing neurologists or other headache specialists, especially if they can’t afford private health care. There is a shortage of health professionals with specialised knowledge about migraine. For example, the Australia and New Zealand Headache Society (ANZHS) keeps a directory of clinicians with an interest in headache. As of 2022, there were only four in New Zealand. A New Zealand online health service directory also lists only three neurologists (some different ones than from the ANZHS directory) with a specified interest in migraine. 

We know there are many more neurologists and specialists who are interested in migraine disease, but it can be difficult to find them.

Prevalence of migraine in Aotearoa New Zealand

The proportion of a population who has a specific disease in a given time period is known as ‘prevalence’. The most recent estimates of the prevalence of migraine in New Zealand come from the New Zealand Health Survey (NZHS), from 2013/14 and the Global Burden of Disease study. 

The NZHS found an overall prevalence of 15.7%, which varied by age and gender. This survey asked whether participants had been told they had migraine by a doctor and did not ask specific questions about migraine symptoms, meaning people with undiagnosed migraine may have been missed. We also cannot identify the proportion of people who are currently experiencing migraine attacks or those who are severely impacted by migraine attacks.

The Global Burden of Disease study estimated that 15.4% of people in New Zealand had migraine in 2019. This was a measure of annual incidence (how many people had the disease in one year). Other studies around the world confirm that migraine is common, affecting around one in seven people. In New Zealand, migraine disease is more common than many other conditions that cause pain or affect the brain and is more prevalent than diabetes, epilepsy and asthma combined.

Based on Global Burden of Disease data (, accessed February 2022)

Migraine in Māori and Pacific people

Our best estimate of the prevalence of migraine disease in Māori or Pacific people in New Zealand comes from the 2013/14 New Zealand Health Survey (NZHS). This found a similar overall prevalence of migraine in Māori (16%), non-Māori (17%) and Pacific people (14%). The lower prevalence in Pacific people was not statistically significant but other research has found that Pacific people are less likely to be diagnosed with migraine, despite having migraine symptoms.

Research from the United States has found that indigenous people have the highest prevalence of migraine of all ethnic groups, and migraine is more common in people who live in poverty.

The burden of migraine disease in these ethnic groups, or any other communities in New Zealand, is unknown.

Given the well-documented inequalities in health outcomes for Māori (and Pacific people) in New Zealand, it’s probable that migraine is not as well recognised and managed in Māori and Pacific people and that the impact of migraine is greater. All New Zealand-specific research and information about migraine must consider and address these inequalities.

Research activity and funding

Despite a growing awareness of the impact of migraine globally, and the development of migraine-specific treatments, we know very little about the burden of migraine disease in New Zealand and very little research has been done on migraine in New Zealand.

The Health Research Council (HRC) is the primary source of Government funding for general health research and spends millions of dollars each year. The HRC has an online library of research projects that it has funded over the past ten years. A search in November 2021 found just one project with relevance to migraine – a study worth $500,000 looking for a new target to treat neurological pain. This study was classified as a ‘rheumatology/arthritis’ study because its main focus was on low back pain.

From the charitable sector, the Neurological Foundation is New Zealand’s leading charity that supports neurological research. However, the Neurological Foundation’s 50th anniversary publication in 2021 reported having allocated only $147,000 to migraine, headache and tinnitus research (combined) in 50 years, from a total funding pool of nearly $52 million. This is despite migraine causing the second highest burden of disability in the world, in global rankings of disease. The only other neurological condition with a similar burden of disability is depression, which commonly co-exists with migraine.

However, the Neurological Foundation did fund a migraine-specific project at the end of 2021 for just over $190,000. This project is looking at calcitonin gene-related peptide (CGRP) receptors in the brain to try and better understand why the new CGRP migraine medications don’t work for everyone. We need research like this, and so much more.