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Apraclonidine 1% w/v Eye Drops, Solution (apraclonidine hydrochloride) Prescribing Information can be found here. Adverse Event Reporting Information can be found at the end of this page.

Keeping intraocular pressure in check

Apraclonidine 1% w/v is indicated to control or prevent post-surgical elevations in intraocular pressure that occur in patients after anterior segment laser surgery. (Clinical trials have been conducted in trabeculoplasty, iridotomy and capsulotomy).1

An elderly person smiling
Photograph of Apraclonidine 1% w/v preservative‑free eye‑drop bottle beside its product box, showing the product label and dosage information.

What is Apraclonidine 1% w/v and how does it work?

Apraclonidine 1% w/v is a potent and relatively selective α2-adrenergic receptor agonist.2 Several studies show that apraclonidine lowers IOP by decreasing aqueous production through its action on α2-adrenoreceptors of the nonpigmented ciliary epithelium.2

Apraclonidine 1% w/v is the only medication licensed for the control or prevention of post-surgical elevations in IOP after anterior segment laser surgery.1,3

Apraclonidine 1% w/v has been used in ophthalmic care for over 3 decades, following its first FDA approval in 1987.4

Clinical trials have documented the efficacy of Apraclonidine 1% w/v in trabeculoplasty, iridotomy and capsulotomy.1

Apraclonidine 1% w/v is available as a preservative-free treatment.5

Could Apraclonidine 1% w/v offer your patients control of IOP spikes following anterior segment laser surgery?

Neodymium-doped yttrium aluminum garnet (Nd:YAG) capsulotomy

Study findings demonstrated that Apraclonidine 1% w/v-treated eyes experienced significantly lower mean change in IOP from baseline to 3 hours post-Nd:YAG capsulotomy compared with placebo-treated eyes.6,7

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Neodymium-doped yttrium aluminum garnet (Nd:YAG) capsulotomy

Apraclonidine 1% w/v-treated eyes demonstrated significantly lower IOP in the 3-hour period following argon laser trabeculoplasty (ALT) compared with placebo-treated eyes in study participants.8

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