Drug Report History

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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 v9-EN Version v4-FR
Language English French
Date Updated 2018-12-04 2018-11-19
Drug Identification Number 02309122 02309122
Brand name PRAMIPEXOLE PRAMIPEXOLE
Common or Proper name PRAMIPEXOLE PRAMIPEXOLE
Company Name SIVEM PHARMACEUTICALS ULC SIVEM PHARMACEUTICALS ULC
Ingredients PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE
Strength(s) 0.25MG 0.25MG
Dosage form(s) TABLET TABLET
Route of administration ORAL ORAL
Packaging size 100 100
ATC code N04BC N04BC
ATC description DOPAMINERGIC AGENTS DOPAMINERGIC AGENTS
Reason for shortage Other (Please describe in comments) Other (Please describe in comments)
Anticipated start date
Actual start date 2017-10-30 2017-10-30
Estimated end date 2018-11-30 2018-12-07
Actual end date 2018-12-03
Shortage status Resolved Actual shortage
Company comments Temporarily unavailable Temporarily unavailable
Health Canada comments