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. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
10% Dextran 40 in 0.9% Sodium chloride 500mL injection bag FKB5043G | 19427 | Medicine | A | 9/30/1991 | |
6% Dextran 70 in 5% Glucose 500mL injection FKB5063G | 19428 | Medicine | A | 9/30/1991 | |
10% Dextran 40 in 5% Glucose 500mL injection FKB5053G | 19426 | Medicine | A | 9/30/1991 | |
6% Dextran 70 in 0.9% Sodium chloride 500mL injection FKB5013G | 19429 | Medicine | A | 9/30/1991 |
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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