TARO-SUNITINIB CAPSULE

Land: Canada

Sprog: engelsk

Kilde: Health Canada

Køb det nu

Hent Produktets egenskaber (SPC)
05-01-2022

Aktiv bestanddel:

SUNITINIB (SUNITINIB MALATE)

Tilgængelig fra:

TARO PHARMACEUTICALS INC

ATC-kode:

L01EX01

INN (International Name):

SUNITINIB

Dosering:

37.5MG

Lægemiddelform:

CAPSULE

Sammensætning:

SUNITINIB (SUNITINIB MALATE) 37.5MG

Indgivelsesvej:

ORAL

Enheder i pakken:

100

Recept type:

Prescription

Produkt oversigt:

Active ingredient group (AIG) number: 0151642004; AHFS:

Autorisation status:

APPROVED

Autorisation dato:

2022-01-07

Produktets egenskaber

                                _Pr_
_TARO-SUNITINIB Product Monograph _
_ Page 1 of 65_
PRODUCT MONOGRAPH
PR
TARO-SUNITINIB
Sunitinib
Capsules
12.5 mg, 25 mg, 37.5 mg, 50 mg sunitinib
per capsule (as sunitinib
malate)
Tyrosine Kinase Inhibitor, Anti-Tumour Agent
Taro Pharmaceuticals Inc.
130 East Drive
Brampton, ON
L6T 1C1
Date of Preparation:
January 5, 2022
Submission
Control No.: 235867
_Pr_
_TARO-SUNITINIB Product Monograph _
_ _
_ _
_ _
_ _
_ _
_ _
_Page 2 of 65 _
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....................................................................................................15
DRUG INTERACTIONS
....................................................................................................30
DOSAGE AND ADMINISTRATION
.................................................................................31
OVERDOSAGE
..................................................................................................................32
ACTION AND CLINICAL
PHARMACOLOGY...............................................................32
STORAGE AND STABILITY
............................................................................................36
SPECIAL HANDLING
INSTRUCTIONS..........................................................................36
DOSAGE FORMS, COMPOSITION AND PACKAGING
................................................36
PART II: SCIENTIFIC INFORMATION
.............................................................................37
PHARMACEUTICAL INFORMATION
.............
                                
                                Læs hele dokumentet
                                
                            

Dokumenter på andre sprog

Produktets egenskaber Produktets egenskaber fransk 05-01-2022

Søg underretninger relateret til dette produkt