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Mydriacyl

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Overview

What is Mydriacyl?

MYDRIACYL® (tropicamide ophthalmic solution, USP) is an anticholinergic prepared as a sterile topical ophthalmic solution in two strengths. The active ingredient is represented by the chemical structure:

Each mL contains: Active:

Preservative:

Inactives:



What does Mydriacyl look like?



What are the available doses of Mydriacyl?

Sorry No records found.

What should I talk to my health care provider before I take Mydriacyl?

Sorry No records found

How should I use Mydriacyl?

For mydriasis and cycloplegia for diagnostic procedures.

For refraction, instill one or two drops of 1% solution in the eye(s), repeated in five minutes. If patient is not seen within 20 to 30 minutes, an additional drop may be instilled to prolong mydriatic effect. For examination of fundus, instill one or two drops of 0.5% solution 15 or 20 minutes prior to examination. Individuals with heavily pigmented irides may require higher strength or more doses. Mydriasis will reverse spontaneously with time, typically in 4 to 8 hours. However, in some cases, complete recovery may take up to 24 hours.


What interacts with Mydriacyl?

Sorry No Records found


What are the warnings of Mydriacyl?

Sorry No Records found


What are the precautions of Mydriacyl?

Sorry No Records found


What are the side effects of Mydriacyl?

Sorry No records found


What should I look out for while using Mydriacyl?

Contraindicated in persons showing hypersensitivity to any component of this preparation.

FOR TOPICAL OPHTHALMIC USE ONLY. NOT FOR INJECTION.

This preparation may cause CNS disturbances which may be dangerous in pediatric patients. The possibility of psychotic reactions and behavioral disturbances due to hypersensitivity to anticholinergic drugs should be considered.

Mydriatics may produce a transient elevation of intraocular pressure.

Remove contact lenses before using.


What might happen if I take too much Mydriacyl?

Sorry No Records found


How should I store and handle Mydriacyl?

3 mL and 15 mL in plastic DROP-TAINER® dispensers.0.5% - 15 mL: 0998-0354-151% -      3 mL: 0065-0355-03            15 mL: 0998-0355-15STORAGE: Rx Only3 mL and 15 mL in plastic DROP-TAINER® dispensers.0.5% - 15 mL: 0998-0354-151% -      3 mL: 0065-0355-03            15 mL: 0998-0355-15STORAGE: Rx Only3 mL and 15 mL in plastic DROP-TAINER® dispensers.0.5% - 15 mL: 0998-0354-151% -      3 mL: 0065-0355-03            15 mL: 0998-0355-15STORAGE: Rx Only3 mL and 15 mL in plastic DROP-TAINER® dispensers.0.5% - 15 mL: 0998-0354-151% -      3 mL: 0065-0355-03            15 mL: 0998-0355-15STORAGE: Rx Only3 mL and 15 mL in plastic DROP-TAINER® dispensers.0.5% - 15 mL: 0998-0354-151% -      3 mL: 0065-0355-03            15 mL: 0998-0355-15STORAGE: Rx Only3 mL and 15 mL in plastic DROP-TAINER® dispensers.0.5% - 15 mL: 0998-0354-151% -      3 mL: 0065-0355-03            15 mL: 0998-0355-15STORAGE: Rx Only


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

This anticholinergic preparation blocks the responses of the sphincter muscle of the iris and the ciliary muscle to cholinergic stimulation, dilating the pupil (mydriasis). The stronger preparation (1%) also paralyzes accommodation. This preparation acts in 15-30 minutes, and the duration of activity is approximately 3-8 hours. Complete recovery from mydriasis in some individuals may require 24 hours. The weaker strength may be useful in producing mydriasis with only slight cycloplegia. Heavily pigmented irides may require more doses than lightly pigmented irides.

Non-Clinical Toxicology
Contraindicated in persons showing hypersensitivity to any component of this preparation.

FOR TOPICAL OPHTHALMIC USE ONLY. NOT FOR INJECTION.

This preparation may cause CNS disturbances which may be dangerous in pediatric patients. The possibility of psychotic reactions and behavioral disturbances due to hypersensitivity to anticholinergic drugs should be considered.

Mydriatics may produce a transient elevation of intraocular pressure.

Remove contact lenses before using.

Tropicamide may interfere with the antihypertensive action of carbachol, pilocarpine, or ophthalmic cholinesterase inhibitors.

The lacrimal sac should be compressed by digital pressure for two to three minutes after instillation to reduce excessive systemic absorption.

Ocular:

Non-Ocular:

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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72
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Tips

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Interactions

Interactions

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