RP Check

Quetiapine

Schedule
S4
Class
Atypical antipsychotic
Indications
2 listed
Brand names

For family members and guardians

A plain-language summary of the cited sources below. Informational only — not medical advice.

Quetiapine is a medication that affects chemical messengers in the brain, particularly serotonin and dopamine. It's most often prescribed to help manage symptoms of schizophrenia, bipolar disorder (including manic episodes and depression linked to bipolar), or to prevent mood episodes from coming back. Doctors sometimes call it an "atypical antipsychotic," which means it works differently from older medications in the same family and tends to cause fewer movement-related side effects.

Your family member might experience some common side effects like drowsiness, headache, dry mouth, dizziness, or constipation, especially when they first start taking it or if the dose changes. These effects don't happen to everyone, and they sometimes lessen over time. More serious side effects can include weight gain, a drop in blood pressure when standing up (which can lead to dizziness or falls), a faster heart rate, or changes in white blood cell counts. If you notice sudden dizziness when they stand, unexplained weight changes, or signs of infection like fever, it's worth discussing with their doctor.

Quetiapine stays in the body for around seven hours, but it's usually taken once or twice a day because the way it affects the brain lasts longer than that short half-life suggests. Some other medications—particularly certain antifungals, antibiotics, and HIV treatments—can increase quetiapine levels in the blood, so it's important that all prescribers know what else your family member is taking.

A Behaviour Support Practitioner will review this medication to determine whether it's being used to manage a mental health condition it's approved for, or whether it's primarily being used to manage behaviours of concern—which may meet the definition of chemical restraint under the NDIS Commission rules and require additional safeguards and regular review.

For prescribers

A plain-language summary of the cited sources below. Informational only — not medical advice.

Quetiapine is a dibenzothiazepine derivative atypical antipsychotic with dual serotonin 5-HT₂ and dopamine D₁/D₂ receptor antagonism, exhibiting higher selectivity for serotonergic receptors—a profile that accounts for its low extrapyramidal liability relative to typical agents. It is PBS-listed for schizophrenia, acute mania, and maintenance treatment of bipolar I disorder (including as monotherapy or adjunct to lithium or valproate for prevention of manic, depressive, or mixed episode relapse), as well as for depressive episodes in bipolar disorder. Quetiapine has a pharmacokinetic half-life of approximately seven hours; however, clinical efficacy supports once- or twice-daily dosing with immediate-release formulations. Metabolism occurs primarily via CYP3A4, and co-administration with potent inhibitors (azole antifungals, macrolide antibiotics, protease inhibitors) can significantly elevate plasma concentrations, requiring dose adjustment. Common adverse effects include somnolence, dizziness, dry mouth, and constipation; serious concerns include orthostatic hypotension, tachycardia, weight gain, leukopenia, and falls—particularly relevant in older adults or those with cardiovascular or metabolic comorbidity.

When quetiapine is prescribed to manage behaviours of concern in an NDIS participant—rather than for a primary psychiatric indication—it meets the NDIS definition of a restrictive practice (chemical restraint) and triggers mandatory documentation and oversight requirements. The Behaviour Support Practitioner reviewing the prescription is verifying that the clinical indication, documented behavioural purpose (if applicable), dosing rationale, and monitoring plan align with the participant's current Behaviour Support Plan and that any behavioural intent has been reported to the NDIS Quality and Safeguards Commission as required under the Restrictive Practices rules. This is a statutory documentation process, not a clinical challenge; the BSP will seek confirmation of your prescribed indication, any behavioural goals documented in your notes, and the frequency of clinical review to satisfy Commission audit standards and ensure alignment between clinical intent and plan-of-record.

§01

Mechanism & pharmacology

Quetiapine and norquetiapine exhibit affinity for brain serotonin (5HT 2 ) and dopamine D 1 and D 2 receptors; this combination of receptor antagonism with a higher selectivity for 5HT 2 relative to D 2 receptors is believed to contribute to the clinical antipsychotic properties and low extrapyramidal side effects (EPS) liability of quetiapine compared to typical antipsychotics.

It has been demonstrated that quetiapine immediate release tablets are effective when given once or twice a day, although quetiapine has a pharmacokinetic half-life of approximately 7 hours.

During concomitant administration of medicines which are potent CYP3A4 inhibitors (such as azole antifungals, macrolide antibiotics and protease inhibitors), plasma concentrations of quetiapine can be significantly higher than observed in patients in clinical trials (see Ketoconazole below).

§02

TGA-approved indications

  • Maintenance treatment of bipolar I disorder, as monotherapy or in combination with lithium or sodium valproate, for the prevention of relapse/recurrence of manic, depressive or mixed episodesTGA PIT1
  • Treatment of depressive episodes associated with bipolar disorderTGA PIT1
§03

PBS-subsidised indications

  • SchizophreniaPBST2
    Show clinical criteria
    Schizophrenia Note: For the purpose of administering this restriction, Schizophrenia refers to schizophrenia spectrum disorders outlined in the DSM-5 criteria.
  • Acute maniaPBST2
    Show clinical criteria
    Acute mania Clinical criteria: Clinical criteria: The condition must be associated with bipolar I disorder, AND The treatment must be as monotherapy, AND The treatment must be limited to up to 6 months per episode. Note: For the purpose of administering this restriction, Schizophrenia refers to schizophrenia spectrum disorders outlined in the DSM-5 criteria.
  • Bipolar I disorderPBST2
    Show clinical criteria
    Bipolar I disorder Clinical criteria: Clinical criteria: The treatment must be maintenance therapy. Note: For the purpose of administering this restriction, Schizophrenia refers to schizophrenia spectrum disorders outlined in the DSM-5 criteria.
§04

Adverse effects

Common (top 5)

Serious

Curated subset. The full adverse-effect list is in the TGA Product Information; click any citation above to open it.

§05

Contraindications

  • patients who are hypersensitive to any component of this productTGA PIT1

Regulated practice context

A plain-language summary of the cited sources below. Informational only — not medical advice.

  • Regulator framework: Quetiapine prescribed to influence behaviour falls under the NDIS Quality and Safeguards Commission's regulated restrictive practices framework as chemical restraint. Implementing providers must hold state/territory authorisation, engage a specialist behaviour support provider, lodge the resulting behaviour support plan with the Commission, and submit monthly reports on the practice's use.NDIS CommissionT2
  • Statutory anchor: the regulated-restrictive-practices framework applied to Quetiapine when prescribed as chemical restraint sits under the National Disability Insurance Scheme Act 2013, the parent statute under which the NDIS (Restrictive Practices and Behaviour Support) Rules 2018 are made and the NDIS Quality and Safeguards Commission operates.NDIS ActT2
  • Commonwealth clinical-quality overlay: Quetiapine use in people with cognitive disability or impairment is governed by the ACSQHC Psychotropic Medicines in Cognitive Disability or Impairment Clinical Care Standard (2024). The Standard's eight quality statements require thorough assessment, non-medication strategies tried first, individualised behaviour planning, clear treatment goals, and regular review with deprescribing where appropriate — applying across all settings where the person receives care.ACSQHC Psychotropic Medicines Clinical Care StandardT2
§07

Jurisdictional framework

Showing Victoria. Other states remain visible below.

Victoria

Restrictive practice framework
  • In Victoria, use of Quetiapine as chemical restraint requires authorisation by the Victorian Senior Practitioner under the Disability Act 2006 (Vic). Authorisation must satisfy the legislative tests of necessity to prevent harm, least-restrictive option, and a documented reduction plan.
  • Statutory anchor: Quetiapine use as chemical restraint in Victoria is regulated by the Disability Act 2006 (Vic), Part 7 of which establishes the Senior Practitioner role and the regulated-restrictive-practice authorisation framework. The Act's tests of necessity, least-restrictive option, and reduction planning are statutorily binding.

Reporting obligations

Victoria
  • NDIS-registered provider
    NDIS CommissionT1
    Reportable to the NDIS Commission as a regulated restrictive practice when used to influence behaviour. Concurrently requires authorisation by the Victorian Senior Practitioner under the Disability Act 2006 (Vic).
    Detail

    NDIS-registered providers in Victoria operate under both the Commonwealth NDIS RP framework (NDIS Rules 2018, reg. 6) and the Victorian RP framework (Disability Act 2006 (Vic), s.143). Use of psychotropic medication as chemical restraint must be authorised by the Senior Practitioner AND reported to the NDIS Commission. Behaviour Support Plan must document the practice, the legislative tests (necessity, least-restrictive option, reduction plan), and the authorising practitioner.

  • Child Safety provider
    SourceT3
    Out-of-home care providers operating under the Children, Youth and Families Act 2005 (Vic) follow DFFH Child Protection frameworks rather than the NDIS RP framework, unless the child is also an NDIS participant in which case both regimes apply.
    Detail

    For dual-funded children (NDIS plan AND Child Protection), the NDIS RP framework applies in addition to the Child Safety framework — chemical restraint authorisation flows through the Victorian Senior Practitioner with concurrent reporting to the NDIS Commission. For non-NDIS children, refer to DFFH Child Protection guidance and clinical-governance pathways through the treating prescriber. This row needs review against current DFFH practice instructions.

  • Health (public hospital / community)
    SourceT3
    Designated mental health services and public hospitals in Victoria operate under the Mental Health and Wellbeing Act 2022 (Vic) — restraint and seclusion provisions are governed by Chief Psychiatrist directives rather than the disability RP framework.
    Detail

    For inpatients receiving compulsory treatment, restraint use is regulated by the Mental Health and Wellbeing Act 2022 (Vic) (replacing the 2014 Act). For voluntary patients without an NDIS plan, common-law consent and clinical-governance frameworks apply. NDIS participants receiving inpatient care may have BOTH the Mental Health Act framework and the NDIS RP framework apply concurrently — review the participant's funding source and treating-team scope before assuming a single framework. This row needs verification against current Chief Psychiatrist guidelines.

  • Aged Care provider
    SourceT2
    Approved aged care providers operate under the Commonwealth Aged Care Act framework — restraint provisions are governed by the Aged Care Quality and Safety Commission's Restrictive Practices framework, parallel to but distinct from the NDIS RP framework.
    Detail

    The aged care RP framework requires informed consent (or substitute decision-maker consent), least-restrictive practice, and documented behaviour support — structurally similar to the NDIS framework but governed by different legislation (Aged Care Act 1997 (Cth) and Quality of Care Principles 2014). For residents under 65 with NDIS plans receiving care in an aged care facility, both regimes can apply. This row needs verification against current Aged Care Commission RP guidance.

  • No NDIS RP reporting obligation; common-law duty of care and Victorian guardianship law apply. Use of psychotropic medication for behavioural reasons remains a chemical restraint regardless of provider registration status — clinical-governance through the prescribing GP or specialist is the operative oversight.
    Detail

    Where a participant is self-managed or family-funded outside any registered provider scheme, formal RP reporting does not flow through the NDIS Commission or DFFH. The treating prescriber retains clinical responsibility under their professional registration; the Mental Health Act guardianship provisions and Powers of Attorney Act 2014 (Vic) frame consent decision-making for participants without capacity. BSPs working with unregulated arrangements should still document the framework analysis even when no reporting authority receives it. This row needs review against current Office of the Public Advocate (Victoria) guidance.

Other jurisdictions (13)
  • NSW: In New South Wales, use of Quetiapine as chemical restraint by a registered NDIS provider must be authorised under the NSW Restrictive Practices Authorisation framework administered by the Department of Communities and Justice (DCJ). Authorisation requires a Behaviour Support Plan documenting the practice, evidence that it is the least-restrictive option, and a documented reduction strategy. Psychotropic medications used as restraint should be reviewed at least every six months by a medical practitioner and at least every twelve months by a psychiatrist.
  • QLD: In Queensland, use of Quetiapine as chemical restraint on an adult with disability requires consent from a restrictive-practices guardian appointed by the Queensland Civil and Administrative Tribunal (QCAT), or short-term approval by the chief executive of the relevant disability service while a Positive Behaviour Support Plan is being developed. The Office of the Public Guardian acts as substitute decision-maker where appointed. Use must be the least-restrictive option to prevent serious harm and is subject to reduction planning.
  • NT: In the Northern Territory, use of Quetiapine as chemical restraint by a registered NDIS service provider requires authorisation by the NT Senior Practitioner via the Restrictive Practice Authorisation System administered by NT Health. Applications must include the Behaviour Support Plan, evidence of consultation with the participant and relevant others, particulars of the providers applying the practice, and a summary of every restrictive practice applied in the preceding 12 months.
  • ACT: In the Australian Capital Territory, use of Quetiapine as chemical restraint is regulated by the Senior Practitioner Act 2018 (ACT), which establishes the Office of the Senior Practitioner with independent oversight across disability services, education, residential care, and child protection. A Positive Behaviour Support Plan must justify the practice as the least-restrictive option, with active reduction strategies. The ACT framework's stated aim is the reduction and elimination of restrictive practices.
  • TAS: In Tasmania, use of Quetiapine as chemical restraint by a disability service provider requires authorisation by the Tasmanian Senior Practitioner under the Disability Rights, Inclusion and Safeguarding Act 2024 (Tas). The Senior Practitioner authorises, oversees, and reports on restrictive practice use in NDIS-funded and Department of Communities Services–funded disability services, with a statutory requirement to protect the rights of people subject to restrictive practices to the greatest extent possible.
  • WA: In Western Australia, use of Quetiapine as chemical restraint requires authorisation through a Quality Assurance Panel under the WA Department of Communities Authorisation of Restrictive Practices framework (effective 1 December 2020). The panel must include at least two decision-makers: a senior manager from the implementing provider and an independent NDIS Behaviour Support Practitioner external to that provider who did not write the Behaviour Support Plan. Unlike single-administrator state models, the panel decision is the authorisation.
  • QLD: In Queensland, use of Quetiapine as chemical restraint by funded disability service providers is governed by the Disability Services Act 2006 (Qld) and the positive behaviour support / restrictive practices framework administered by the Department of Families, Seniors, Disability Services and Child Safety. Authorisation must follow assessment by an appropriately qualified practitioner, a Positive Behaviour Support Plan, and the legislative tests of least-restrictive practice and reduction planning. Authorisation is granted per restrictive-practice type — separate authorisation is required for each.
  • SA: In South Australia, use of Quetiapine as chemical restraint is a Level 2 restrictive practice under the SA Restrictive Practices Authorisation Scheme (in force from 30 May 2022) and can only be authorised by the Senior Authorising Officer — Authorised Program Officers cannot approve chemical restraint. Authorisation requires a Behaviour Support Plan, advice from a Specialist Behaviour Support Practitioner, and consultation with the participant and their family. The scheme is administered by the Restrictive Practices Unit within the Department of Human Services.
  • TAS: Statutory anchor: Quetiapine use as chemical restraint by disability service providers in Tasmania is regulated by the Disability Rights, Inclusion and Safeguarding Act 2024 (Tas), which establishes the Tasmanian Senior Practitioner with statutory powers to authorise, oversee, and report on restrictive-practice use in NDIS-funded and Department of Communities Services–funded disability services.
  • SA: Statutory anchor: Quetiapine use as chemical restraint in South Australia is regulated by the Disability Inclusion Act 2018 (SA), with the operative detail in the Disability Inclusion (Restrictive Practices — NDIS) Regulations 2021. Together they establish the two-tier authorisation scheme (Authorised Program Officer for Level 1, Senior Authorising Officer for Level 2 including chemical restraint) in force from 30 May 2022.
  • QLD: Statutory anchor: substitute decision-making for Quetiapine use as chemical restraint on adults with impaired capacity in Queensland is governed by the Guardianship and Administration Act 2000 (Qld). Chapter 5B Part 4 sets out QCAT's powers to appoint a restrictive-practices guardian and the Office of the Public Guardian's role as substitute decision-maker.
  • ACT: Statutory anchor: Quetiapine use as chemical restraint in the ACT is regulated by the Senior Practitioner Act 2018 (ACT). The Act's stated object is the reduction and elimination of restrictive practices and it applies broader-than-NDIS oversight: disability services, education, residential care, and child protection all sit within scope.
  • QLD: Statutory anchor: Quetiapine use as chemical restraint by funded disability service providers in Queensland is regulated by the Disability Services Act 2006 (Qld), Chapter 5B of which sets out the positive behaviour support and restrictive-practice authorisation framework. The PBSRP Reform Bill 2024 lapsed in October 2024; the existing framework remains in force.
Reference page·RP Check is informational, not clinical advice·a PracticeWise project

The reasoning structure on this page is largely transferable to the parallel aged-care restrictive-practices framework administered by the Aged Care Quality and Safety Commission. The Commonwealth statute (Aged Care Act 1997) governs in place of the NDIS Rules; the medication-context analysis is otherwise the same.