IPG-CANDESARTAN TABLET

Država: Kanada

Jezik: angleščina

Source: Health Canada

Aktivna sestavina:

CANDESARTAN CILEXETIL

Dostopno od:

MARCAN PHARMACEUTICALS INC

Koda artikla:

C09CA06

INN (mednarodno ime):

CANDESARTAN

Odmerek:

16MG

Farmacevtska oblika:

TABLET

Sestava:

CANDESARTAN CILEXETIL 16MG

Pot uporabe:

ORAL

Enote v paketu:

30/1000

Tip zastaranja:

Prescription

Terapevtsko območje:

ANGIOTENSIN II RECEPTOR ANTAGONISTS

Povzetek izdelek:

Active ingredient group (AIG) number: 0135220003; AHFS:

Status dovoljenje:

APPROVED

Datum dovoljenje:

2016-08-19

Lastnosti izdelka

1
PRODUCT MONOGRAPH
PR
IPG-CANDESARTAN
Candesartan Cilexetil Tablets
4 mg, 8 mg, 16 mg and 32 mg
Angiotensin II AT
1
Receptor Blocker
Date of Preparation:
August 19, 2016
Marcan Pharmaceuticals Inc.
77 Auriga Drive, Suite #4
Ottawa, Ontario
K2E 7Z7
CONTROL# 196962
2
TABLE OF CONTENTS
CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
...........................................................................................
3
SUMMARY PRODUCT INFORMATION
........................................................................................................
3
INDICATIONS AND CLINICAL
USE................................................................................................................
3
CONTRAINDICATIONS
.................................................................................................................................
4
WARNINGS AND PRECAUTIONS
.................................................................................................................
4
ADVERSE REACTIONS
.................................................................................................................................
8
DRUG INTERACTIONS
...............................................................................................................................
14
DOSAGE AND ADMINISTRATION
..............................................................................................................
17
OVERDOSAGE
...........................................................................................................................................
20
ACTION AND CLINICAL PHARMACOLOGY
................................................................................................
20
STORAGE AND
STABILITY..........................................................................................................................
23
DOSAGE FORMS, COMPOSITION AND PACKAGING
.................................................................................
23
PART II: SCIENTIFIC INFORMATION
.....................