ACH-APIXABAN TABLET

Kraj: Kanada

Język: angielski

Źródło: Health Canada

Kup teraz

Składnik aktywny:

APIXABAN

Dostępny od:

ACCORD HEALTHCARE INC

Kod ATC:

B01AF02

INN (International Nazwa):

APIXABAN

Dawkowanie:

2.5MG

Forma farmaceutyczna:

TABLET

Skład:

APIXABAN 2.5MG

Droga podania:

ORAL

Sztuk w opakowaniu:

15G/50G

Typ recepty:

Prescription

Podsumowanie produktu:

Active ingredient group (AIG) number: 0153051001; AHFS:

Status autoryzacji:

APPROVED

Data autoryzacji:

2022-09-23

Charakterystyka produktu

                                PRODUCT MONOGRAPH
PR
ACH-APIXABAN
Apixaban Tablets
2.5 mg and 5 mg
Anticoagulant
Accord Healthcare Inc.
3535 boul. St. Charles, Suite 704
Kirkland, QC, H9H 5B9
Canada
Date of Initial Approval:
April 23, 2019
Date of Revision:
September 22, 2022
Submission
Control No: 264541
_Pr_
_ACH-APIXABAN Product Monograph Page 2 of 77 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL
INFORMATION...........................................................
3
SUMMARY PRODUCT INFORMATION
..........................................................................
3
INDICATIONS AND CLINICAL
USE................................................................................
3
CONTRAINDICATIONS
....................................................................................................
4
WARNINGS AND PRECAUTIONS
...................................................................................
4
ADVERSE REACTIONS
...................................................................................................10
DRUG
INTERACTIONS....................................................................................................19
DOSAGE AND
ADMINISTRATION.................................................................................24
OVERDOSAGE
.................................................................................................................31
ACTION AND CLINICAL PHARMACOLOGY
................................................................32
STORAGE AND
STABILITY............................................................................................37
SPECIAL HANDLING INSTRUCTIONS
..........................................................................37
DOSAGE FORMS, COMPOSITION AND PACKAGING
..................................................37
PART II: SCIENTIFIC
INFORMATION................................................................................38
PHARMACEUTICAL
INFORMATION.............................................................................38
CLINICAL TRIALS
..........................
                                
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