Coat the Cornea, See the Difference in the eyes of cystinosis patients

CYSTADROPS dissolves corneal cystine crystals across all layers

40% decrease in corneal cystine crystals after 90 days of use
Efficacy maintained over 5 years with well-managed daily use

With practical, 4 times a day dosing

Cystadrops dissolving corneal cystine crystals

Clinical Data & Safety

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How CYSTADROPS Works

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Prescribing CYSTADROPS

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Indications and Usage

CYSTADROPS^® (cysteamine ophthalmic solution) 0.37% is a cystine-depleting agent indicated for the treatment of corneal cystine crystal deposits in adults and children with cystinosis.

Important Safety Information

Contamination of Tip and Solution: To minimize the risk of contamination, do not touch the dropper tip to any surface. Keep bottle tightly closed when not in use.
Benign Intracranial Hypertension: Benign intracranial hypertension (or pseudotumor cerebri) associated with oral cysteamine or ophthalmic use of cysteamine (with concurrent oral cysteamine) has been reported, which has resolved with diuretic therapy.
Contact Lens Use: Contains benzalkonium chloride. Contact with soft contact lenses should be avoided. Remove contact lenses prior to application. Lenses may be reinserted 15 minutes following administration.
The most common adverse reactions (≥ 10%) are eye pain, vision blurred, eye irritation, ocular hyperaemia, instillation site discomfort, eye pruritus, lacrimation increased, and ocular deposits.
To report SUSPECTED ADVERSE REACTIONS, contact Recordati Rare Diseases Inc. at 1-888-575-8344, or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

CYSTADROPS^® (cysteamine ophthalmic solution), for topical ophthalmic use, is available as 3.8 mg/mL of cysteamine (0.37%) in 5 mL bottles.

INDICATIONS AND IMPORTANT SAFETY INFORMATION

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Important Safety Information

Contamination of Tip and Solution: To minimize the risk of contamination, do not touch the dropper tip to any surface. Keep bottle tightly closed when not in use.