Clinical drug

netarsudil 0.2 MG/ML Ophthalmic Solution

0.2 MG/ML · Ophthalmic Solution · ophthalmic

A form of netarsudil

netarsudil 0.2 MG/ML Ophthalmic Solution — Prostaglandin analogues. INDICATIONS AND USAGE RHOPRESSA is indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular h

netarsudil 0.2 MG/ML Ophthalmic Solution

Active ingredient

Classification

Prostaglandin analoguesRho Kinase Inhibitor

Drug interactions

The label indicates potential interactions with specific eye drop formulations.

  • unknownthimerosal — precipitation can occur when mixed with ROCKLATAN
  • moderateprostaglandins or prostaglandin analogs — combined use is not recommended and may decrease IOP lowering effect or cause paradoxical elevations in IOP

Indications

INDICATIONS AND USAGE RHOPRESSA is indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. RHOPRESSA ® is a Rho kinase inhibitor indicated for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension. ( 1 )

Dosage

DOSAGE AND ADMINISTRATION The recommended dosage is one drop in the affected eye(s) once daily in the evening. If one dose is missed, treatment should continue with the next dose in the evening. Twice a day dosing is not well tolerated and is not recommended. If RHOPRESSA is to be used concomitantly with other topical ophthalmic drug products to lower IOP, administer each drug product at least 5 minutes apart [see Patient Counseling Information ( 17 )]. One drop into the affected eye(s) once daily in the evening. ( 2 )

Warnings

WARNINGS AND PRECAUTIONS 5.1 Epithelial Corneal Edema Epithelial corneal edema, described as honeycomb or bullous, has been reported in some patients with pre-existing corneal stromal edema or following ocular procedures that could affect corneal endothelial function. Epithelial corneal edema typically resolves upon discontinuation of RHOPRESSA. Advise patients to notify their physician if they experience eye pain or decreased vision while using RHOPRESSA [see Adverse Reactions ( 6.2 ) and Patient Counselling Information ( 17 )] . 5.2 Bacterial Keratitis There have been reports of bacterial keratitis associated with the use of multiple-dose containers of topical ophthalmic products. These containers had been inadvertently contaminated by patients who, in most cases, had a concurrent corneal disease or a disruption of the ocular epithelial surface [see Patient Counseling Information ( 17 )]. 5.3 Use with Contact Lenses Contact lenses should be removed prior to instillation of RHOPRESSA and may be reinserted 15 minutes following its administration.

Contraindications

CONTRAINDICATIONS None. None. ( 4 )

Mechanism of action

Mechanism of Action Netarsudil is a rho kinase inhibitor, which is believed to reduce IOP by increasing the outflow of aqueous humor through the trabecular meshwork. The exact mechanism is unknown.

Indicated ICD-10 codes

Source: RxNorm + openFDA + RxClass + FAERS · 2026

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