Monday, October 10, 2016

Emedastine Difumarate


Class: Antiallergic Agents
ATC Class: S03AA07
VA Class: OP900
Chemical Name: 1-(2-Ethoxyethyl)-2-(hexahydro-4-methyl-1H-1,4-diazepin-1-yl)benzimidazole fumerate (1:2)
Molecular Formula: C17H26N4O•2C4H4O4
CAS Number: 87233-62-3
Brands: Emadine

Introduction

Relatively selective histamine H1-receptor antagonist;1 2 3 14 a benzimidazole derivative.1 12


Uses for Emedastine Difumarate


Allergic Conjunctivitis


Symptomatic relief of allergic conjunctivitis.1


Emedastine Difumarate Dosage and Administration


Administration


Apply topically to the eye as an ophthalmic solution.1 Not for injection or oral use.1


Ophthalmic Administration


Remove soft contact lenses prior to administration of each dose (since benzalkonium chloride preservative may be absorbed by the lenses); may reinsert lenses 10 minutes after administration if eyes are not red.1


If more than one topical ophthalmic drug is used, administer the drugs at least 5 minutes apart.12


Avoid contamination of the solution container.1


Do not use if solution is discolored.1


Dosage


Available as emedastine difumarate; dosage expressed in terms of emedastine.1


Pediatric Patients


Allergic Conjunctivitis

Ophthalmic

Children ≥3 years of age: 1 drop of a 0.05% solution in the affected eye(s) up to 4 times daily.1


Adults


Allergic Conjunctivitis

Ophthalmic

1 drop of a 0.05% solution in the affected eye(s) up to 4 times daily.1


Cautions for Emedastine Difumarate


Contraindications



  • Known hypersensitivity to emedastine or any ingredient in the formulation.1



Warnings/Precautions


Specific Populations


Pregnancy

Category B.1


Lactation

Distributed into milk in rats following oral administration;1 not known whether distributed into human milk following topical application to the eye.1 Use with caution.1


Pediatric Use

Safety and efficacy not established in children <3 years of age.1


Adverse effect profile in children 3–16 years of age is similar to that in individuals ≥17 years of age.14


Geriatric Use

No substantial differences in safety and efficacy relative to younger adults.1


Common Adverse Effects


Headache.1


Interactions for Emedastine Difumarate


No formal drug interaction studies to date.12


Emedastine Difumarate Pharmacokinetics


Absorption


Bioavailability


Limited systemic exposure following topical application to the eye;1 plasma concentrations usually are undetectable.1 12


Onset


Rapid onset.2 14


Duration


Long duration.2 14


Elimination


Metabolism


Metabolized in the liver principally to 5- and 6-hydroxyemedastine following oral administration; metabolites appear to undergo further oxidation to form 5′-oxo analogs.1 12


Elimination Route


44% of an oral dose is recovered in urine within 24 hours.1


Half-life


3–4 hours following oral administration.1


Stability


Storage


Ophthalmic


Solution

Tightly closed bottle at 4–30°C.1


ActionsActions



  • Inhibits the histamine-stimulated conjunctival vascular permeability response in a concentration-dependent manner.1 2




  • Potency is about 100, 357, or 5813 times that of levocabastine, pheniramine, or antazoline, respectively, on a molar basis.2 14



Advice to Patients



  • Importance of learning and adhering to proper administration techniques to avoid contamination of the solution container.1 12




  • Importance of removing soft contact lenses prior to administration of each dose.1 Delay reinsertion for 10 minutes after administration if eyes are not red; do not wear contact lenses if eye(s) are red.1 Not indicated for contact lens-related irritation.1




  • Importance of administering different topical ophthalmic preparations at least 5 minutes apart.1




  • Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.1




  • Importance of informing clinicians of existing or contemplated therapy, including prescription and OTC drugs as well as any concomitant illnesses.




  • Importance of informing patients of other important precautionary information.1 (See Cautions.)



Preparations


Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.













Emedastine Difumarate

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Ophthalmic



Solution



0.05% (of emedastine)



Emadine (with benzalkonium chloride)



Alcon



Disclaimer

This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.


The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.

AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions July 2005. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.




References



1. Alcon Laboratories Inc. Emadine (emedastine difumarate) ophthalmic solution 0.05% prescribing information. Forth Worth, TX; 2003 Aug.



2. Yanni JM, Stephens DJ, Parnell DW et al. Preclinical efficacy of emedastine, a potent, selective histamine H1 antagonist for topical ocular use. J Ocular Pharmacol. 1994; 10:665-75.



3. Sharif NA, Su SX, Yanni JM. Emedastine: a potent, high affinity histamine H1 receptor-selective antagonist for ocular use: receptor binding and second messenger studies. J Ocular Pharmacol. 1994; 10:653-64.



4. Fukuda T, Saito T, Yoshidomi M et al. Influence of 1-(2-ethoxyethyl)-2-(4-methyl-1-homopiperazinyl)benzimidazole difumarate (KB-2413), a new antiallergic, on ciliary movement. Arzneimittelforschung. 1984; 34:816-8. [PubMed 6149756]



5. Budavari S, O’Neil MJ, Smith A et al, eds. The Merck index. 12th ed. Rahway, NJ: Merck & Co, Inc; 1996:601.



6. Ciprandi G, Buscaglia S, Cerqueti PM et al. Drug treatment of allergic conjunctivitis: a review of the evidence. Drugs. 1992; 43:154-76. [IDIS 360840] [PubMed 1372215]



7. Morrow GL, Abbott RL. Conjunctivitis. Am Fam Physician. 1998; 57:735-46. [IDIS 418448] [PubMed 9490996]



8. Titi MJ. A critical look at ocular allergy drugs. Am Fam Physician. 1996; 53:2637-42. [IDIS 367250] [PubMed 8644576]



9. Galindez OA, Kaufman HE. Coping with the itchy-burnies: the management of allergic conjunctivitis. Ophthalmology. 1996; 103:1335-6. [IDIS 373485] [PubMed 8841290]



10. Friedlaender MH. Current concepts in ocular allergy. Ann Allergy. 1991; 67:5-10,13. [IDIS 312766] [PubMed 1859041]



11. Trocme SD. Medical therapy for ocular allergy. Mayo Clin Proc. 1992; 67:557-65. [IDIS 296611] [PubMed 1359206]



12. Alcon Laboratories; Fort Worth, TX: Personal communication.



13. Reviewers’ comments (personal observations).



14. Alcon Laboratories. Emadine (emedastine difumarate) ophthalmic solution 0.05% product monograph. Fort Worth, TX: (not dated).



15. Verin P, Secchi A, Easty DL et al. Efficacy and safety of emedastine eye drops 0.05% compared to levocabastine eye drops 0.05% in allergic conjunctivitis. Invest Ophthalmol Vis Sci. 1998; 39:S549.



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