Nesudil Ophthalmic Solution: Each ml contains Netarsudil Dimesylate INN equivalent to Netarsudil 0.20 mg
Preservative: Sodium Perborate BP 0.01%
Nesudil is indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension
The recommended dosage is one drop in the affected eye(s) once daily in the evening
This eye drop is contraindicated in patients who are hypersensitive to any component of this preparation
For ophthalmic use only.
To avoid possible contamination of the drops, do not touch the dropper tip or to any surface.
Netarsudil can be used with other topical eye drug products, but they should be administered at least 5 minutes apart from each other.
Contact lenses should be removed prior to installation of Netarsudil and may be reinserted 15 minutes following its administration.
The most common ocular adverse reaction observed in controlled clinical studies with Netarsudil was conjunctival hyperemia, corneal verticillata, instillation site pain, corneal staining and blurred vision
This document does not contain possible drug interactions
Pregnancy: There are no adequate and well-controlled studies of Netarsudil ophthalmic solution in pregnant women to inform any drug-associated risk. However, systemic exposure to Netarsudil from ocular administration is low.
Lactation: There are no data on the presence of Netarsudil in human milk, the effects on the breastfed infant, or the effects on milk production.
Pediatric Use: Safety and effectiveness in pediatric patients below the age of 18 years have not been established.
Use in elderly patients: No overall differences in safety and effectiveness have been observed between elderly and other adult patients.
Nesudil Ophthalmic Solution: Each LDPE dropper bottle contains 3 ml of Sterile Eye Drops
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