Drug Report History

Return to report

Below you will find the report version history. When a report is updated, a new version of the report is created. The report history allows you to see the changes between versions. You can select two versions of the report to compare. The fields that were changed between versions will be highlighted in yellow.

The translation of reports creates two separate versions which is why some reports may not seem to have any differences. In this case, only the language field below will be highlighted in yellow.

Version v7-FR Version v1-EN
Language French English
Date Updated 2021-06-22 2021-04-26
Drug Identification Number 02020939 02020939
Brand name SCLERODEX SCLERODEX
Common or Proper name Dextrose USP 250mg/mL with Sodium Chloride USP 100mg/mL Dextrose USP 250mg/mL with Sodium Chloride USP 100mg/mL
Company Name OMEGA LABORATORIES LIMITED OMEGA LABORATORIES LIMITED
Ingredients DEXTROSE SODIUM CHLORIDE DEXTROSE SODIUM CHLORIDE
Strength(s) 250MG 100MG 250MG 100MG
Dosage form(s) LIQUID LIQUID
Route of administration INTRAVENOUS INTRAVENOUS INTRAVENOUS INTRAVENOUS
Packaging size 50 x 10mL vial / fiole 50 x 10mL vial / fiole
ATC code C05BB C05BB
ATC description ANTIVARICOSE THERAPY ANTIVARICOSE THERAPY
Reason for shortage Disruption of the manufacture of the drug. Disruption of the manufacture of the drug.
Anticipated start date
Actual start date 2021-04-26 2021-04-26
Estimated end date 2021-06-18 Unknown
Actual end date 2021-06-18
Shortage status Resolved Anticipated shortage
Tier 3 Status No No
Company comments
Health Canada comments