PRIVA-CANDESARTAN TABLET

Land: Canada

Taal: Engels

Bron: Health Canada

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Download Productkenmerken (SPC)
16-06-2016

Werkstoffen:

CANDESARTAN CILEXETIL

Beschikbaar vanaf:

PHARMAPAR INC

ATC-code:

C09CA06

INN (Algemene Internationale Benaming):

CANDESARTAN

Dosering:

32MG

farmaceutische vorm:

TABLET

Samenstelling:

CANDESARTAN CILEXETIL 32MG

Toedieningsweg:

ORAL

Eenheden in pakket:

100

Prescription-type:

Prescription

Therapeutisch gebied:

ANGIOTENSIN II RECEPTOR ANTAGONISTS

Product samenvatting:

Active ingredient group (AIG) number: 0135220004; AHFS:

Autorisatie-status:

CANCELLED PRE MARKET

Autorisatie datum:

2018-03-06

Productkenmerken

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_Page 1 of 35 _
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PRODUCT MONOGRAPH
PR
PRIVA-CANDESARTAN
Candesartan Cilexetil Tablets
4 mg, 8 mg, 16 mg and 32 mg
Angiotensin II AT
1
Receptor Blocker
PHARMAPAR INC.
DATE OF PREPARATION:
5950, Côte de Liesse, Suite 100
June 15, 2016
Ville Mont-Royal
Québec H4T 1E2
SUBMISSION CONTROL #: 194899
_Priva-CANDESARTAN _
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_Page 2 of 35 _
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TABLE OF CONTENTS
CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
...............................................................................
3
SUMMARY PRODUCT INFORMATION
...............................................................................................
3
INDICATIONS AND CLINICAL USE
.....................................................................................................
3
CONTRAINDICATIONS
..........................................................................................................................
4
WARNINGS AND PRECAUTIONS
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4
ADVERSE REACTIONS
...........................................................................................................................
8
DRUG INTERACTIONS
.........................................................................................................................
13
DOSAGE AND ADMINISTRATION
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16
OVERDOSAGE
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19
ACTION AND CLINICAL
PHARMACOLOGY....................................................................................
19
STORAGE AND STABILITY
.................................................................................................................
21
DOSAGE FORMS, COMPOSITION AND PACKAGING
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