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ELESTAT

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Overview

What is ELESTAT?

ELESTAT

Epinastine HCl is represented by the following structural formula:

Chemical Name:

Each mL contains: Active:

Preservative:

Inactives:

ELESTAT



What does ELESTAT look like?



What are the available doses of ELESTAT?

Ophthalmic solution containing 0.5 mg/mL epinastine HCl. ()

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

How should I use ELESTAT?

ELESTAT

®

The recommended dosage is one drop in each eye twice a day.

Treatment should be continued throughout the period of exposure (i.e., until the pollen season is over or until exposure to the offending allergen is terminated), even when symptoms are absent.


What interacts with ELESTAT?

Sorry No Records found


What are the warnings of ELESTAT?

Sorry No Records found


What are the precautions of ELESTAT?

Sorry No Records found


What are the side effects of ELESTAT?

Sorry No records found


What should I look out for while using ELESTAT?

None


What might happen if I take too much ELESTAT?

Sorry No Records found


How should I store and handle ELESTAT?

Handling and DisposalHandle and dispose of Doxorubicin Hydrochloride Injection consistent with recommendations for the handling and disposal of hazardous drugs. Handling and DisposalHandle and dispose of Doxorubicin Hydrochloride Injection consistent with recommendations for the handling and disposal of hazardous drugs. ELESTAT5 mL in 10 mL bottle                  NDC 0023-9201-05 ELESTAT5 mL in 10 mL bottle                  NDC 0023-9201-05


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

Epinastine is a topically active, direct H-receptor antagonist and an inhibitor of the release of histamine from the mast cell. Epinastine is selective for the histamine H-receptor and has affinity for the histamine H-receptor. Epinastine also possesses affinity for the α, α -, and 5-HT–receptors.

Non-Clinical Toxicology
None

Renal toxicity has been reported in a few patients with liver dysfunction who were given oral cholecystographic agents followed by intravascular contrast agents. Administration of intravascular agents should therefore be postponed in any patient with a known or suspected hepatic or biliary disorder who has recently received a cholecystographic contrast agent.

Other drugs should not be admixed with iopamidol.

Patients should be instructed to avoid allowing the tip of the dispensing container to contact the eye, surrounding structures, fingers, or any other surface in order to avoid contamination of the solution by common bacteria known to cause ocular infections. Serious damage to the eye and subsequent loss of vision may result from using contaminated solutions.

Bottle should be kept tightly closed when not in use.

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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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Review

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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

Tips

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Interactions

Interactions

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