Isopto Hyoscine: Indications, Dosage, Precautions, Adverse Effects
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Isopto Hyoscine - Product Information

Manufacture: Alcon
Country: United States
Condition: Iridocyclitis
Class: Mydriatics
Form: Liquid solution, Eye drops (ophthalmic)
Ingredients: Scopolamine Hydrobromide (Scopolamine), Benzalkonium Chloride, Hypromelloses, Sodium Chloride, Acetic Acid, Sodium Acetate, Water

(scopolamine hydrobromide ophthalmic solution) Sterile

Description Section

Isopto Hyoscine (scopolamine hydrobromide ophthalmic solution) is an anticholinergic prepared as a sterile topical ophthalmic solution. The active ingredient is represented by the chemical structure:

Established name: scopolamine hydrobromide

Chemical name: benzeneacetic acid, α-(hydroxymethyl)-, 9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]non-7-yl ester, hydrobromide, trihydrate, [7(S)-(1α,2β,4β,5α,7β)]-.

Each mL contains: Active: scopolamine hydrobromide 0.25%. Preservative: benzalkonium chloride 0.01%. Vehicle: hypromellose 0.5%. Inactives: sodium chloride, glacial acetic acid, sodium acetate (to adjust pH), purified water.

Clinical Pharmacology Section

This anticholinergic preparation blocks the responses of the sphincter muscle of the iris and the accommodative muscle of the ciliary body to cholinergic stimulation, producing pupillary dilation (mydriasis) and paralysis of accommodation (cycloplegia).

Indications & Usage Section

For mydriasis and cycloplegia in diagnostic procedures. For some pre- and postoperative states when a mydriatic and cycloplegic is needed in treatment of iridocyclitis.

Contraindications Section

Contraindicated in persons with primary glaucoma or a tendency toward glaucoma, e.g., narrow anterior chamber angle; and in those showing hypersensitivity to any component of this preparation.

Warnings Section

Do not touch dropper tip to any surface, as this may contaminate the solution.

FOR TOPICAL OPHTHALMIC USE ONLY - NOT FOR INJECTION.

Precautions Section

To avoid excessive absorption, the lacrimal sac should be compressed by digital pressure for two to three minutes after instillation. To avoid inducing angle closure glaucoma, an estimation of the depth of the angle of the anterior chamber should be made.

Patient Warning

Patient should be advised not to drive or engage in other hazardous activities when drowsy or while pupils are dilated. Patient may experience sensitivity to light and should protect eyes in bright illumination during dilation. Parents should be warned not to get this preparation in their child’s mouth and to wash their own hands and the child’s hands following administration.

Pediatric Use

Safety and effectiveness in pediatric patients have not been established.

Geriatric Use

No overall differences in safety or effectiveness have been observed between elderly and younger patients.

Adverse Reactions Section

Prolonged use may produce local irritation, characterized by follicular conjunctivitis, vascular congestion, edema, exudate, and an eczematoid dermatitis. Somnolence, dryness of the mouth, or visual hallucinations may occur.

Dosage & Administration Section

For refraction, administer one or two drops in the eye(s) one hour before refracting. For uveitis, administer one or two drops in the eye(s) up to four times daily.

How Supplied Section

In 5 mL plastic DROP-TAINER dispensers.

5 mL NDC 0998-0331-05

Storage Section

Store at 8°-27°C (46°-80°F). Protect from light.