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Dextran

Generic Name
Dextran
Brand Names
Bion Tears, Colirio Ocusan, Genteal Tears, Genteal Tears Mild, Tears Naturale, Tears Renewed
Drug Type
Small Molecule
CAS Number
9004-54-0

Overview

Dextran is a polysaccharide that differs from others in that its glucose units are joined together 1:6 glucoside links. The main chain of glucose has short branches at frequent intervals which are probably joined by 1:3 and 1:4 glucoside links. The chains can be composed of about 200,000 glucose units. Many bacteria, like Leuconostoc, can synthesize dextran from sucrose, and this activity is used commercially to obtain dextran. Dextran 40 is a sterile, nonpyrogenic preparation of low molecular weight dextran (average mol. wt. 40,000) in 5% Dextrose Injection or 0.9% Sodium Chloride Injection. It is administered by intravenous infusion. Dextran 75 is a complex branched glucan with an average molecular weight 75000 Daltons. It is produced from certain bacteria that with α-1,6 glycosidic linkages between glucose molecules and α-1,3 linkages between branches. When labelled with technetium Tc99m, dextran 75 is intravenously administered as an imaging agent to detect and diagnose conditions in the vascular compartment such as pericardial effusion or ventricular aneurysm.

Indication

Dextran is used as the restoration of blood mass during surgical interventions if there is hypovolemia due to trauma or dehydration. It is as well used after the presence of hemorrhage in cases of blood loss to a level inferior to 15% of the blood mass, if compatibility test cannot be completed or when blood lots need to be tested for pathogen detection. Dextran is also used for the prevention of profound postoperative venous thrombosis. Dextran as well presents ophthalmic applications as solutions or ointments for the temporary relief of xerophthalmia or minor ocular irritations.

Associated Conditions

  • Blood Circulation Disorder
  • Capillary disorder
  • Dry Eyes
  • Ocular Irritation
  • Pulmonary Embolism
  • Pulmonary Embolism caused by procedures associated with a high incidence of thromboembolic complications
  • Shock
  • Thrombosis
  • Venous Thrombosis (Disorder)
  • Venous Thrombosis caused by procedures associated with a high incidence of thromboembolic complications

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2022/09/07
N/A
ENROLLING_BY_INVITATION
2022/04/06
Phase 4
Completed
Andover Research Eye Institute
2022/03/04
Phase 4
Completed
Andover Research Eye Institute
2021/08/17
N/A
Recruiting
2018/02/15
Not Applicable
UNKNOWN
LanZhou University
2017/07/07
Not Applicable
Completed
Huaxia Eye Hospital Group
2017/03/03
Phase 2
Completed
2017/02/23
Not Applicable
UNKNOWN
Tung Wah Hospital
2016/12/14
Not Applicable
UNKNOWN
Sun Yat-sen University
2016/08/11
Phase 1
Completed
Joseph B. Ciolino, MD

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Hospira, Inc.
0409-7419
INTRAVENOUS
10 g in 100 mL
2/15/2023
Hospira, Inc.
0409-7418
INTRAVENOUS
10 g in 100 mL
2/15/2023
DLC Laboratories, Inc.
24286-1575
OPHTHALMIC
1 mg in 1 mL
4/18/2025
Preferred PHarmaceuticals Inc.
68788-8635
OPHTHALMIC
0.1 g in 100 mL
5/7/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
LMD 10% IN DEXTROSE 5%
00224235
Solution - Intravenous
10 %
12/31/1968
GENTRAN 40 10% SODIUM CHLORIDE 0.9% INJ
baxter corporation
00454923
Liquid - Intravenous
10 G / 100 ML
12/31/1979
6% DEXTRAN 70 IN 0.9% SODIUM CHLORIDE INJECTION
b. braun medical inc
01924192
Solution - Intravenous
6 %
9/10/1996
LMD 10% IN 0.9% SODIUM CHLORIDE
00224227
Solution - Intravenous
10 %
12/31/1968
VISINE FOR RED EYE WORKPLACE
johnson & johnson inc
02436086
Drops - Ophthalmic
0.1 % / W/V
6/3/2016
VISINE FOR RED EYE COOL
johnson & johnson inc
02328399
Drops - Ophthalmic
0.1 % / W/V
4/15/2010
TEARS NATURALE
Alcon Canada Inc
00390291
Solution - Ophthalmic
0.1 %
12/31/1977
RHEOMACRODEX 10% IN NORMAL SALINE
pharmacia (canada) inc.
00213926
Liquid - Intravenous
10 G / 100 ML
12/31/1962
AQUASITE DPS
02029901
Drops - Ophthalmic
.1 %
12/31/1993
ADVANCED RELIEF EYE DROPS
juno otc inc
02344319
Solution - Ophthalmic
0.1 % / W/V
8/30/2010

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
DACROLUX 3MG/ML +1MG/ML COLIRIO EN SOLUCIÓN
Reva Health Europe S.L.
58742
COLIRIO EN SOLUCIÓN
Sin Receta
Not Commercialized
RHEOMACRODEX 10% SALINO
Fresenius Kabi España, S.A.U.
39627
SOLUCIÓN PARA PERFUSIÓN
Uso Hospitalario
Not Commercialized

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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