Most medication in a SIL house goes fine, which is exactly why the records slip — until a missed dose or an audit puts them under a light. Getting medication management right is part good practice, part paper trail, and part knowing the one line that turns a routine PRN into a regulated restrictive practice. Here's all three.

Who this is for

You run SIL houses where workers support participants with medication. This sits across safe service delivery, governance, and — at its edge — restrictive practices.

The basics: Webster packs and the MAR

Pharmacy-prepared Webster packs (dose administration aids) reduce error and make administration checkable — each labelled with the participant's name and dosage. Every dose then lands on a medication administration record (MAR): given, missed, refused or delayed, each one recorded. And each participant needs a current medication management plan — what's prescribed, how it's given, side effects to watch, and what to do in an emergency.

What a support worker can and can't do

In a SIL setting, a support worker generally reminds, assists a participant to take their medication correctly, records what happened, and reports concerns to the right clinician. They don't prescribe, don't change a dose, and don't make the clinical call. Keeping that scope clear — in policy and in practice — is what an auditor checks.

The line into restrictive practice

Here's the one that catches people: a medication used primarily to influence behaviour, rather than to treat a diagnosed condition, is chemical restraint — a regulated restrictive practice. That means it needs a current behaviour support plan, state or territory authorisation, and reporting. A PRN sedative given 'to settle' someone, with no plan behind it, is an unauthorised restrictive practice — and a reportable incident.

When it goes wrong: med errors

A missed dose, a wrong dose, an adverse reaction — document it, escalate it, and follow your incident process. If it meets the threshold, it's a reportable incident with the usual clock running. The error isn't the only thing being assessed; what you did next is.

Common questions

What is a medication administration record (MAR)?
A record of every dose given, missed, refused or delayed, kept for each participant.

When is a medication a restrictive practice?
When it's used primarily to influence behaviour rather than to treat a diagnosed condition — that's chemical restraint, which needs a behaviour support plan and authorisation.

What can a support worker do with medication?
Remind, assist a participant to take it correctly, record it, and report concerns — not prescribe, change a dose, or make clinical decisions.

Where Clearline fits — honestly

Aura OS by Clearline Health reads Webster packs to set up the medication record (AI for admin), keeps the MAR against each participant, links a behaviour-influencing medication to its behaviour support plan so a chemical restraint can't sit unauthorised, and turns a med error into an incident with the clock attached. When the auditor asks, the 60-second audit test packages it — pick a participant, a date and a Practice Standard, and a branded PDF is in their inbox in two clicks.

Flat $49 a month, same price for two houses or twenty. The free tier is unlimited — workers, participants and houses — with every audit-ready feature included. Audit-ready on free. AI for admin, humans for care. Australian-owned and Sydney-hosted; the few US sub-processors we use — error reporting, payments, AI — are each named in our privacy policy.

Honest about the limit: AI reads the pack, but humans give the medication, and the clinical decisions stay with clinicians. What software does is keep the record straight and flag the line you can't cross without a plan.

Pass your audit without losing your weekend.

Start free — every audit-ready feature included, no credit card.

General information drawn from the NDIS Practice Standards, medication guidance and the restrictive practices rules, not clinical or medical advice. Medication scope and training requirements vary — check the current rules with the NDIS Commission, your state or territory, and the participant's prescriber and pharmacist.