EIKANCE · LOW-DOSE ATROPINE
Eikance eye drops for myopia control
Low-dose atropine slows myopia progression in children. We prescribe Eikance directly — and explain when low-dose atropine is the right concentration for your child.
Reviewed by Dr Mark Joung · Last updated 11 May 2026
800+
Ortho-K Lenses Fitted
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EIKANCE EYE DROPS
What is Eikance?
A TGA-approved low-dose atropine eye drop
Atropine has been used in eye care for more than a century. At the doses used to control myopia in children, it works very differently to the higher doses ophthalmologists use for other conditions — the side effects are minimal at 0.01%, and most children notice little difference day to day.
Manufactured by Aspen Pharmacare Australia, Eikance is the only TGA-registered low-dose atropine for myopia in Australia. It's available at 0.01% (registered since 2021) and 0.05% (registered since February 2026).
SUITABILITY
Who is low-dose atropine for?
Children with progressing myopia, ages 4 to 14
We typically recommend low-dose atropine for children whose short-sightedness is progressing measurably year on year — either by prescription change or by axial length growth on our IOLMaster 500.
Good candidates
Not suitable for
- Children with angle-closure glaucoma or a family history of it
- Children with a known atropine allergy
- Children who cannot reliably have a drop instilled each evening
CONCENTRATION CHOICE
Choosing the right strength
Concentration matters more than brand
| Concentration | Source | When we prescribe it | Approx. cost / month |
|---|---|---|---|
| 0.01% | Eikance only | Combination therapy with Ortho-K or MiyoSmart, where atropine boosts the primary treatment | ~$50 |
| 0.025% | Compounded | Monotherapy — mild to moderate progression where Ortho-K and MiyoSmart aren't suitable or wanted | ~$40–50 |
| 0.05% | Compounded → Eikance (transitioning) | Monotherapy — faster progressors needing stronger dose response | ~$50 |
We match the concentration to clinical need first, then use the TGA-approved product where it's available at that concentration. Eikance 0.01% is the only option at the low dose (legally, 0.01% atropine cannot be compounded while a registered product exists). Eikance 0.05% became available in February 2026 and we're transitioning patients across as scripts are renewed. The 0.025% strength remains compounded because no TGA-registered version exists.
This approach follows the Pharmacy Board of Australia Guidelines on Compounding of Medicines, which state a medicine should not be compounded if a suitable commercial product is available. For us, that means TGA-approved Eikance where it exists at the strength clinically indicated — not a brand preference, a regulatory and clinical alignment. For a deeper look at the atropine clinical research including the LAMP study, see our dedicated atropine page.