Description

The most common ocular adverse reaction observed in controlled clinical studies with Netarsudil & Latanoprost was conjunctival hyperemia, instillation site pain, corneal verticillata, instillation site discomfort, foreign body sensation and blurred visions were reported in few patients.

There are no adequate and well-controlled studies of Netarsudil & Latanoprost combination in pregnant women to inform any drug-associated risk. There are no data on the presence of Netarsudil or Latanoprost in human milk, the effects on the breastfed infant, or the effects on milk production.

For ophthalmic use only To avoid possible contamination of the drops, do not touch the dropper tip or to any surface Should be used with caution in patients with active intraocular inflammation (e.g., iritis/uveits) May cause changes to pigmented tissues, gradually change eyelashes and vellus hair in the treated eye Cystoid macular edema, has been reported during treatment with Latanoprost. Reactivation of Herpes Simplex keratitis may occur Netarsudil & Latanoprost combination can be used with other topical eye drug products, but they should be administered at least 5 minutes apart from each other.

Pediatric Use: Safety and effectiveness in pediatric patients have not been established. Use in elderly patients: No overall differences in safety and effectiveness have been observed between elderly and other adult patients.

Drugs for miotics and glaucoma

Store at 2°-8°C in a dry place, protect from light until opened. After opening the product may be kept at 2°-25°C for upto 6 weeks. Keep out of the reach of children.