Legacy pregnancy categoryNot assigned — PLLR-era drug
Defining liabilityGenerally tolerated at therapeutic doses; clinically important risks are agent-specific and increase with interactions or organ impairment.
Elevated IOP in open-angle glaucoma or ocular hypertension
adult
1 drop affected eye(s) QHS
1 drop affected eye(s) QHS
1 drop QD (evening)
Renal Undefined
Hepatic Undefined
If a dose is missed, resume with the next evening dose
Instructions
Instill one drop in the affected eye(s) once daily in the evening; twice-daily dosing not recommended
If using other topical IOP drugs, separate administration by at least 5 minutes
Remove contact lenses before instillation; may reinsert 15 minutes after
Available strengths
drops 0.02 %
Cautions
Epithelial corneal edema in pre-existing corneal stromal edema or after procedures affecting the endothelium
Bacterial keratitis with contaminated multi-dose containers
Remove contact lenses before use
Adverse reactions
Conjunctival hyperemia (53%)
Corneal verticillata (~20%)
Instillation site pain
Conjunctival hemorrhage
Pregnancy No human data; systemic exposure low; IV animal studies showed embryofetal harm at high exposures
Lactation No data; low systemic exposure after topical ocular use
Cost
Netarsudil (RHOPRESSA)
Strength
#/mo
generic $/unit
CostPlus
0.02 %
drops
per unit
not offered
NADAC is a voluntary CMS survey of what retail community pharmacies pay for the drugs they stock. Netarsudil is dispensed outside retail pharmacies, so it rarely appears on surveyed invoices.