MYLAN-DULOXETINE CAPSULE (DELAYED RELEASE)

Država: Kanada

Jezik: engleski

Izvor: Health Canada

Aktivni sastojci:

DULOXETINE (DULOXETINE HYDROCHLORIDE)

Dostupno od:

MYLAN PHARMACEUTICALS ULC

ATC koda:

N06AX21

INN (International ime):

DULOXETINE

Doziranje:

60MG

Farmaceutski oblik:

CAPSULE (DELAYED RELEASE)

Sastav:

DULOXETINE (DULOXETINE HYDROCHLORIDE) 60MG

Administracija rute:

ORAL

Jedinice u paketu:

30/100/500

Tip recepta:

Prescription

Područje terapije:

SELECTIVE SEROTONIN AND NOREPINEPHRINE-REUPTAKE INHIBITORS

Proizvod sažetak:

Active ingredient group (AIG) number: 0152350002; AHFS:

Status autorizacije:

CANCELLED POST MARKET

Datum autorizacije:

2018-05-10

Svojstava lijeka

_MYLAN-DULOXETINE Product Monograph_
Page 1 of 86
PRODUCT MONOGRAPH
PR MYLAN-DULOXETINE
Duloxetine Delayed Release Capsules, Mylan Standard
Duloxetine (as duloxetine hydrochloride)
30 mg and 60 mg
ANALGESIC/ANTIDEPRESSANT/ANXIOLYTIC
Mylan Pharmaceuticals ULC
85 Advance Road
Etobicoke, ON
M8Z 2S6
Submission Control No.: 198303
Date of Revision: September 29, 2016
_MYLAN-DULOXETINE Product Monograph_
Page 2 of 86
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.................................................................. 3
SUMMARY PRODUCT INFORMATION
...............................................................................
3
INDICATIONS AND CLINICAL USE
.....................................................................................
3
CONTRAINDICATIONS
...........................................................................................................
5
WARNINGS AND PRECAUTIONS
.........................................................................................
6
ADVERSE REACTIONS
.........................................................................................................
19
DRUG INTERACTIONS
.........................................................................................................
38
DOSAGE AND ADMINISTRATION
.....................................................................................
42
OVERDOSAGE
........................................................................................................................
45
ACTION AND CLINICAL PHARMACOLOGY
....................................................................
46
STORAGE AND STABILITY
.................................................................................................
49
DOSAGE FORMS, COMPOSITION AND PACKAGING
..................................................... 49
PART II: SCIENTIFIC INFORMATION
.........................................................................................
51
PHARMACEUTICAL INFORMATION
.....................................................