Duralub Eg Eye
Duralub Eg Eye Uses, Dosage, Side Effects, Food Interaction and all others data.
The higher strength of Carboxymethylcellulose Sodium USP-NF provides long-lasting relief from dryness by forming a soothing gel after administration of the drops on to the eyes.
In a randomized clinical study of patients with mild or moderate forms of eye dryness, ophthalmic treatment with sodium carboxymethylcellulose resulted in a diminished frequency of symptoms compared to the placebo group . Carboxymethylcellulose interacts with human corneal epithelial cells to facilitate corneal epithelial wound healing and attenuate eye irritation in a dose-dependent manner . It exhibits protective actions on the ocular surface in various applications; it mediates cytoprotective effects on the ocular surface when applied prior to contact lenses and reduces the incidence of epithelial defects during LASIK .
| Trade Name | Duralub Eg Eye |
| Generic | Carboxymethylcellulose + Glycerine |
| Weight | 0.3%w/w |
| Type | Gel |
| Therapeutic Class | |
| Manufacturer | Austrak Pvt Ltd |
| Available Country | India |
| Last Updated: | September 19, 2023 at 7:00 am |
Uses
Carboxymethylcellulose Sodium is used as a lubricant to relieve irritation and discomfort due to dryness of the eye or due to exposure to wind or sun.
Duralub Eg Eye is also used to associated treatment for these conditions: Dry Eyes, Ocular Irritation
How Duralub Eg Eye works
Carboxymethylcellulose binds to the surface of corneal epithelial cells via its glucopyranose subunits binding to glucose receptors GLUT-1 . The residence time of carboxymethylcellulose bound to corneal cells is approximately 2 hours as indicated by a short-term binding assay . Binding of carboxymethylcellulose to the matrix proteins stimulated corneal epithelial cell attachment, migration, and re-epithelialization of corneal wounds .
Dosage
Duralub Eg Eye dosage
Install 1 or 2 drops in the affected eye(s) as needed or as directed by the physician.
Side Effects
Visual disturbances, ocular discharge and eye pruritus are common adverse drug reactions were reported with Carboxymethylcellulose Sodium
Toxicity
Rat oral LD50, rabbit dermal LD50, and rat inhalation LC50 of sodium carboxymethyl cellulose are 27000 mg/kg, >2 g/kg, and >5800 mg/m^3 (4 hours), respectively .
Precaution
Concomitant ocular medication should be administered 15 minutes apart to the instillation of this eye drop.
Interaction
No information is available.
Volume of Distribution
No pharmacokinetic data available.
Elimination Route
No pharmacokinetic data available.
Half Life
No pharmacokinetic data available.
Clearance
No pharmacokinetic data available.
Elimination Route
No pharmacokinetic data available.
Pregnancy & Breastfeeding use
Use in Pregnancy: There is no data on the use of Carboxymethylcellulose Sodium 1% during pregnancy and lactation in human. Animal studies did not show harmful effects with the active ingredient Carboxymethylcellulose Sodium. Use in Lactation: Carboxymethylcellulose Sodium is not absorbed systemically; there is no known potential for excretion in human breast milk.
Pediatric use: The safety and effectiveness in pediatric patients have not been established.
Contraindication
Contraindicated in patients who are hypersensitive to any of the components of Carboxymethylcellulose Sodium.
Special Warning
Use in children: No information available.
Use in elderly patients: No information available.
Acute Overdose
Since CMC is pharmacologically inert and not expected to be absorbed systemically, systemic effects from topical overdose are not expected from the administration of Carboxymethylcellulose sodium (Cellufresh) 0.5%. Additionally, no toxic side effects are expected should accidental systemic overdose occur.
Storage Condition
Store in a cool, dry place and protect from light. Keep out of the reach of children.
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