Last updated: October 2026
Eye drops for presbyopia went from idea to prescription in four years. Three products are now FDA-approved, and a pilocarpine drop reached the Indian market amid controversy. Patients will ask whether they can "throw away their reading glasses", so residents need to know how these drops work, how well, and who should avoid them.
| Pilocarpine 1.25% (Vuity) | Pilocarpine 0.4% (Qlosi) | Aceclidine 1.44% (Vizz) | |
|---|---|---|---|
| FDA approval | October 2021 | October 2023 | July 2025 |
| Mechanism | Muscarinic agonist acting on iris and ciliary muscle | Low-dose pilocarpine, preservative-free | Predominantly pupil-selective miotic |
| Pivotal trials | GEMINI 1 and 2: significant gain of at least 3 lines of near vision in low light at day 30, hour 3, without losing more than 1 line of distance vision | NEAR-1 and NEAR-2 (600+ patients): significant gain of at least 3 lines of distance-corrected near vision without losing distance vision | CLARITY 1 and 2 (n=466, 42 days); CLARITY 3 (6-month safety) |
| Onset and duration | About 15 minutes, lasting up to about 6 hours | About 20 minutes, lasting up to about 8 hours. Can be used up to twice daily. | Within 30 minutes, lasting up to about 10 hours |
| Common side effects | Headache, ocular redness | Headache 6.8%, instillation pain 5.8% | Instillation irritation 20%, dim vision 16%, headache 13% |
A pilocarpine 1.25% drop (PresVu, Entod Pharmaceuticals) received approval from the Drugs Controller General of India in 2024. In September 2024 the regulator suspended its manufacturing and marketing permission, citing promotional claims, such as removing the need for reading glasses, that went beyond what was approved. The company challenged the order. Check its current status before advising patients, and use the episode as a lesson in matching expectations to evidence.
Related: refractive surgery for residents, monovision in cataract surgery and IOL types.
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