Guide ยท ADHD medication
ADHD medication: what it is, how it works and the risks
ADHD medication in Australia means one of a small group of prescription medicines: three stimulants and a few non-stimulants. This guide covers how they work, what the research shows, their side effects and the rules around prescribing.
Updated 25 September 2026 · About 8 minutes to read · All guides
In short
- The ADHD medicines registered in Australia are three stimulants (methylphenidate, dexamfetamine and lisdexamfetamine) and two non-stimulants (atomoxetine, and guanfacine for ages 6 to 17); clonidine is also used, off-label.
- Stimulants boost two brain chemical messengers, dopamine and noradrenaline, and in short-term trials reduce core ADHD symptoms more than placebo in children and adults.
- The Australian ADHD guideline recommends a stimulant as the first medicine to try where symptoms cause significant impairment, with non-stimulants offered if stimulants don't suit or don't work.
- Common side effects include reduced appetite, poor sleep, headache, stomach ache, irritability and small rises in heart rate and blood pressure.
- Stimulants are Schedule 8 controlled medicines, and each state and territory sets its own rules on who can prescribe them.
Which medicines are used for ADHD in Australia
ADHD medicines fall into two groups. Stimulants are usually tried first. Non-stimulants are used when stimulants aren't suitable, don't help enough or cause side effects.
| Medicine | Type | What the TGA has registered it for | Notes |
|---|---|---|---|
| Methylphenidate (Ritalin, Ritalin LA, Concerta) | Stimulant | ADHD (long-acting forms not established under 6) | Short-acting about 3 to 4 hours; long-acting about 6 to 12 hours |
| Dexamfetamine | Stimulant | ADHD in children (not under 3) and narcolepsy; the guideline also recommends it for adults | Short-acting tablet, about 4 to 6 hours |
| Lisdexamfetamine (Vyvanse) | Stimulant | ADHD (not studied under 6), and binge eating disorder in adults | Once-daily capsule, about 6 to 12 hours |
| Atomoxetine | Non-stimulant | ADHD, age 6 and over | Full effect can take up to 8 weeks |
| Guanfacine (Intuniv) | Non-stimulant | ADHD, ages 6 to 17, alone or with a stimulant | Can cause sleepiness and low blood pressure |
| Clonidine | Non-stimulant | Not registered for ADHD (off-label use) | Can cause sleepiness and low blood pressure |
Off-label means prescribed outside the use the TGA approved. The Australian guideline includes some off-label options, such as guanfacine for adults.
For more on individual medicines, see our guides to lisdexamfetamine (Vyvanse), dexamfetamine and methylphenidate (Ritalin and Concerta).
How stimulants and non-stimulants work
Stimulants increase the activity of dopamine and noradrenaline, two chemical messengers in the brain. They slow the reabsorption of these messengers and increase their release. Healthdirect describes the result as improvements in behaviour, impulsiveness, attention and memory.
Stimulants work only while the dose is active. Short-acting forms start soon after a dose and wear off within hours; long-acting forms start more slowly and last longer.
Atomoxetine blocks the reabsorption of noradrenaline only. It builds up gradually: it takes one to two weeks to reach a steady level and can take up to eight weeks to reach full effect. Guanfacine and clonidine act on a particular type of noradrenaline receptor (alpha-2 receptors); clonidine can also have a calming effect.
No ADHD medicine suits everyone. Stimulants work differently in different people, and if one doesn't help, the doctor may try another.
What the research shows
A 2018 network meta-analysis in The Lancet Psychiatry (Cortese and colleagues) pooled 133 double-blind randomised trials comparing ADHD medicines with each other or with placebo. The main efficacy analysis covered about 10,000 children and teenagers and 8,000 adults, at around 12 weeks.
- In children and teenagers, every medicine studied reduced symptoms more than placebo on clinician ratings. Amphetamines (including lisdexamfetamine) had the largest average effect, then methylphenidate, then atomoxetine.
- In adults, amphetamines, methylphenidate, bupropion and atomoxetine did better than placebo; modafinil did not.
- More people stopped amphetamines than placebo because of side effects, in both age groups. In adults this was also true of methylphenidate and atomoxetine, and in children, of guanfacine.
Weighing benefits against side effects, the authors favoured methylphenidate for children and teenagers, and amphetamines for adults, as first choices for short-term treatment.
A 2025 review of adult treatments (Ostinelli and colleagues, 113 trials, 14,887 adults) found stimulants and atomoxetine were the only treatments with evidence of reducing core symptoms in the short term, on both self-ratings and clinician ratings. More people stopped atomoxetine than placebo. Medication did not clearly improve quality of life, and most trials lasted three months or less, so long-term benefit is less certain.
The Australian guideline, developed by the Australasian ADHD Professionals Association (AADPA), recommends methylphenidate, dexamfetamine or lisdexamfetamine as the first medicine to try where ADHD symptoms cause significant impairment. Its authors judged the evidence not certain enough to set different first choices by age. If stimulants don't suit or haven't worked at adequate doses, it recommends atomoxetine or guanfacine (and for children, clonidine). For young children, a paediatrician or child psychiatrist should assess first, and medication should be used cautiously.
Side effects and who needs to be careful
Common side effects
Healthdirect lists the most common stimulant side effects as reduced appetite, weight loss, increased anxiety and irritability, trouble sleeping, stomach ache and headache. Stimulants can slow a child's growth in height, and twitches (tics) of the face or neck can start. Guanfacine and clonidine can cause sleepiness, dizziness and low blood pressure.
Heart rate and blood pressure
A 2025 analysis of 102 trials (22,702 people, median length 7 weeks) found stimulants and atomoxetine caused small average rises in blood pressure and heart rate, while guanfacine lowered them. Some individuals may have larger changes, so the authors advised checking blood pressure and pulse on any ADHD medicine.
Longer-term evidence comes from observational studies. A Swedish study drawn from 278,027 people with ADHD found each extra year of medication use was linked to about a 4% higher risk of cardiovascular disease, mainly high blood pressure and artery disease. This is an association, not proof of cause.
Less common but serious
Stimulants can worsen mood or anxiety, and rarely cause psychotic or manic symptoms at usual doses. Too much can cause overdose, especially in children, so store medicines out of reach. Stopping guanfacine suddenly can make blood pressure and heart rate rise.
Who may not be able to take them
Stimulants are generally not used by people who:
- take, or have taken in the past 14 days, a type of antidepressant called an MAOI
- have heart disease causing symptoms, or glaucoma
- have untreated mania or psychosis
- are currently misusing drugs or alcohol
A family history of sudden death or certain inherited heart conditions usually means a heart check first. Non-stimulants may be used when a condition such as Tourette syndrome rules out stimulants. Pregnancy, planned pregnancy and breastfeeding change the balance of risks and need discussing with the prescriber.
Schedule 8 rules and who can prescribe
Methylphenidate, dexamfetamine and lisdexamfetamine are Schedule 8 medicines, also called controlled drugs. Schedule 8 medicines have special rules to reduce the risk of misuse or dependence, covering how they are supplied, sold, owned and used. Each state and territory sets its own rules, and prescribers may need a permit or authority from the health department.
In general terms:
- For under-18s, starting a stimulant is restricted in most states and territories to paediatricians and child and adolescent psychiatrists. Queensland is the exception.
- For adults, treatment is usually started by a psychiatrist. Some jurisdictions now allow trained GPs to diagnose and prescribe.
- In some states, GPs can continue a prescription under set conditions, such as a specialist diagnosis and regular specialist review.
These rules have changed several times recently, so check the current position with your state or territory health department.
Misuse and diversion (medicine ending up with someone it wasn't prescribed for) of ADHD stimulants are common, and prescribers are expected to check real-time prescription monitoring before each script or review. Prescription medicines must only be taken by the person they are prescribed for; giving or selling them to someone else is illegal.
Medication is one part of treatment
The Australian ADHD guideline recommends non-medication support alongside, or instead of, medicine:
- parent and family training for parents of children with ADHD
- cognitive-behavioural therapy for teenagers and adults, and as an option for children
- guidance on lifestyle, such as a healthy and active routine
If medication is used, the guideline recommends checking heart rate and blood pressure before and after each dose change and every six months. For children and teenagers it recommends measuring height every six months and tracking weight. Medicines shouldn't be stopped without talking to the doctor, as some need to be reduced slowly.
Questions to ask the prescriber
- Why this medicine and form, rather than the alternatives?
- How long does one dose last, and when should it be taken?
- Which side effects are expected, and which mean we should contact you?
- How and how often will heart rate, blood pressure, height and weight be checked?
- How will we judge whether it is working, and when is the next review?
- Does it interact with other medicines, alcohol or health conditions?
- What non-medication support should go alongside it?
- How would we stop it safely, if we decided to?
This guide is general information, not medical advice. Decisions about starting, changing or stopping ADHD medication are made with the prescribing doctor.
Questions people ask
What does ADHD medication do?
ADHD medicines reduce the core symptoms of ADHD, such as inattention, hyperactivity and impulsivity, while they are working. Stimulants increase the activity of dopamine and noradrenaline in the brain; non-stimulants act mainly on noradrenaline. Response varies between people, and evidence on long-term benefit is limited.
What medication is used for ADHD in Australia?
The stimulants methylphenidate (Ritalin, Ritalin LA, Concerta), dexamfetamine and lisdexamfetamine (Vyvanse) are usually tried first. The non-stimulants atomoxetine and guanfacine (Intuniv) are registered for ADHD too, with guanfacine registered for ages 6 to 17. Clonidine is also used, off-label.
What are the side effects of ADHD medication?
The most common stimulant side effects are reduced appetite, weight loss, trouble sleeping, stomach ache, headache, and increased anxiety or irritability. Stimulants can also slow children's growth in height and slightly raise heart rate and blood pressure. Guanfacine and clonidine can cause sleepiness and low blood pressure.
Can a GP prescribe ADHD medication in Australia?
It depends on the state or territory, because stimulants are Schedule 8 medicines regulated locally. In most places, stimulants for children are started by a paediatrician or child and adolescent psychiatrist, and for adults usually by a psychiatrist. Some jurisdictions now let trained GPs diagnose and prescribe, and some let GPs continue a prescription under set conditions.
Is ADHD medication safe long term?
Most trials last about three months or less, so long-term evidence comes mainly from observational studies. A large Swedish study found each extra year of use was linked to a slightly higher risk of cardiovascular disease, mainly high blood pressure, though this does not prove cause. The Australian guideline recommends checking heart rate and blood pressure every six months, and growth in children.
Where this information comes from
We would rather you checked us than took our word for it. Every link below is the original source, not a summary of one.
- Cortese et al. (2018). Comparative efficacy and tolerability of medications for attention-deficit hyperactivity disorder in children, adolescents, and adults: a systematic review and network meta-analysis. The Lancet Psychiatry.Network meta-analysis of 133 double-blind trials comparing ADHD medicines on short-term (about 12-week) symptom reduction and tolerability in children and adults.
- Ostinelli et al. (2025). Comparative efficacy and acceptability of pharmacological, psychological, and neurostimulatory interventions for ADHD in adults: a systematic review and component network meta-analysis. The Lancet Psychiatry.Review of 113 trials in 14,887 adults finding short-term symptom benefit for stimulants and atomoxetine, no clear quality-of-life gain, and little long-term evidence.
- Farhat et al. (2025). Comparative cardiovascular safety of medications for attention-deficit hyperactivity disorder in children, adolescents, and adults: a systematic review and network meta-analysis. The Lancet Psychiatry.Analysis of 102 short trials (22,702 people) measuring changes in blood pressure and heart rate with each ADHD medicine.
- Zhang et al. (2024). Attention-Deficit/Hyperactivity Disorder Medications and Long-Term Risk of Cardiovascular Diseases. JAMA Psychiatry.Swedish case-control study linking longer cumulative ADHD medication use with a modestly higher risk of cardiovascular disease, mainly hypertension and arterial disease.
- Australasian ADHD Professionals Association (2022). Australian Evidence-Based Clinical Practice Guideline for ADHD: Summary of Recommendations.The national guideline's recommendations on first- and second-line medicines, non-medication treatments and monitoring.
- Australasian ADHD Professionals Association. Australian ADHD Clinical Practice Guideline: 5.2 Medication Choice.Explains why the guideline recommends any of the three stimulants first rather than setting different first choices by age.
- Healthdirect. ADHD medicines (last reviewed December 2025).Government-funded plain-English overview of ADHD medicines, how they work, side effects, prescribing controls and stopping safely.
- Efron & Coscini (2025). Pharmacological management of attention deficit hyperactivity disorder in children and adolescents. Australian Prescriber.Australian prescribing review covering how each medicine works, duration of action, side effects, heart screening and who can start stimulants for under-18s.
- Suetani, Hull & Scott (2026). Pharmacological management of attention deficit hyperactivity disorder in adults. Australian Prescriber.Australian review listing each medicine's TGA-registered indication, contraindications, misuse and diversion, and who initiates adult treatment.
- Takeda Pharmaceuticals Australia. Intuniv (guanfacine) Consumer Medicine Information.Confirms guanfacine's registered use for ADHD in ages 6 to 17, alone or with a stimulant, and the warning against stopping suddenly.
- Takeda Pharmaceuticals Australia. Vyvanse Australian Product Information (revised April 2026).Approved product information, used here for the stimulant class warning about psychotic or manic symptoms at usual doses.
- Healthdirect. Scheduling of medicines and poisons.Plain-English definition of Schedule 8 controlled drugs.
- NSW Health. Prescribe a psychostimulant medicine.Confirms dexamfetamine, lisdexamfetamine and methylphenidate are Schedule 8 in NSW, which specialists hold class authority, and the GP pathways.
- Victorian Department of Health. Stimulants for ADHD or narcolepsy: permit requirements.Victoria's permit rules for Schedule 8 stimulants, including when GPs can prescribe.
- SA Health. Schedule 8 medicine treatment.Explains what a Schedule 8 authority is and states it is illegal to supply your prescription drug to another person.
Links to external sites are provided for reference. We do not control them and they may change. Last checked 25 September 2026.