Sandimmum Neoral100 mg

Sandimmum Neoral 100 mg Ophthalmic Emulsion is indicated to increase tear production in patients whose tear production is presumed to be suppressed due to ocular inflammation associated with dry eye syndrome (keratoconjunctivitis sicca).In addition to this, several clinical studies have showed that Sandimmum Neoral 100 mg is effective in the management of different eye diseases like vernal keratoc…

One drop of Sandimmum Neoral 100 mg eye drop should be instilled twice a day in each eye approximately 12 hours apart. Sandimmum Neoral 100 mg eye drop can be used concomitantly with artificial tears, allowing a 15-minute interval between products.

The most common adverse event was ocular burning. Other events reported included conjunctival hyperemia, discharge, epiphora, eye pain, foreign body sensation, pruritus, stinging, and visual disturbance (most often blurring).

Sandimmum Neoral 100 mg is contraindicated in patients with active ocular infections and in patients with known or suspected hypersensitivity to any of the ingredients in the formulation.

Sandimmum Neoral 100 mg eye drop should not be administered while wearing contact lenses. Patients with decreased tear production typically should not wear contact lenses. If contact lenses are worn, they should be removed prior to the administration of this formulation. Lenses may be reinserted 15 minutes following administration of Sandimmum Neoral 100 mg eye drop.

Pregnancy: There are no adequate and well-controlled studies of Sandimmum Neoral 100 mg Ophthalmic Emulsion in pregnant women. It should be administered to pregnant women if clearly needed. Lactation: Sandimmum Neoral 100 mg is known to be excreted in human milk following systemic administration but excretion in human milk after topical treatment has not been investigated. Although blood concentra…