Inflavis (Dexamethasone sodium phosphate) ophthalmic solution is a clear, colorless to pale yellow topical steroid solution for ophthalmic or otic administration.
Dexamethasone is a synthetic analog of naturally occurring glucocorticoids (hydrocortisone and cortisone). Dexamethasone sodium phosphate is a water soluble, inorganic ester of dexamethasone. It is approximately three thousand times more soluble in water at 25?C than hydrocortisone.

Inflavis Ophthalmic Solution is indicated for the treatment of different type of eye and ear disorder.

For Eye: Dexamethasone Phosphate is indicated for treatment of steroid responsive inflammatory conditions of the conjunctiva, cornea and anterior segment of the eye such as: anterior uveitis, iritis, cyclitis, allergic and vernal conjunctivitis, herpes zoster keratitis, superficial punctate keratitis and non-specific superficial keratitis. Also indicated for the treatment of corneal injury from chemical, radiation or thermal burns or following penetration by foreign bodies. Inflavis indicated for post-operative use to reduce inflammatory reactions and suppress graft reaction.

For Ear: Indicated in the steroid responsive inflammatory conditions of the external auditory meatus, such as allergic otitis externa, selected purulent and non-purulent infective otitis externa.

Administration of dexamethasone to the eye may rarely cause stinging, burning, redness or watering of the eyes. Topically applied dexamethasone is not recommended in breastfeeding mothers, as it is possible that traces of dexamethasone may enter the breast milk.

Every plastic dropper bottle contains 5 ml sterile eye drops. Each ml contains Dexamethasone Sodium Phosphate USP equivalent to Dexamethasone Phosphate 1 mg.

Saloride? contains Sodium Chloride 0.9% sterile isotonic aqueous solution. 0.9% Sodium Chloride is used in intra-ocular surgeries and it facilitates the wearing and removing of contact lens of the lens users.

Saloride? is used as required, depending upon the purpose of use.

Every plastic Dropper bottle contains 10 ml of 0.9% Sodium Chloride and each ml drop contain Sodium Chloride BP 9mg.

Xidolac? (ketorolac) ophthalmic solution is supplied as a sterile isotonic aqueous 0.5% solution.

ketorolac is a member of the pyrrolo-pyrrole group of nonsteroidal anti-inflammatory drugs (NSAIDs) for ophthalmic use.

Xidolac? (Ketorolac tromethamine) is indicated for seasonal allergic conjunctivitis and for pain and inflammation in ocular surgery. It is also indicated for the treatment of postoperative inflammation in patients who have undergone cataract extraction.

The recommended dose of Xidolac? ophthalmic solution is one drop four times a day in the operated eye as needed for pain and burning/stinging for up to 5 days following corneal refractive surgery.
Reported adverse reactions for Ketorolac ophthalmic solution occurring in approximately 1 to 5% people were conjunctival hyperemia, corneal infiltrates, headache, ocular edema and ocular pain.

The most frequent adverse events reported with the use of ketorolac tromethamine ophthalmic solutions have been transient stinging and burning on instillation.

Ketorolac tromethamine ophthalmic solution has been safely administered in conjunction with other ophthalmic medications such as antibiotics, beta blockers, carbonic anhydrase inhibitors, cycloplegics, and mydriatics. Every plastic dropper bottle contains 5 ml sterile eye drops. Each ml contains ketorolac tromethamine 5 mg.