AA-CLOZAPINE TABLET

Valsts: Kanāda

Valoda: angļu

Klimata pārmaiņas: Health Canada

Nopērc to tagad

Lejuplādēt Produkta apraksts (SPC)
03-04-2023

Aktīvā sastāvdaļa:

CLOZAPINE

Pieejams no:

AA PHARMA INC

ATĶ kods:

N05AH02

SNN (starptautisko nepatentēto nosaukumu):

CLOZAPINE

Deva:

50MG

Zāļu forma:

TABLET

Kompozīcija:

CLOZAPINE 50MG

Ievadīšanas:

ORAL

Vienības iepakojumā:

100/500

Receptes veids:

Prescription

Ārstniecības joma:

ATYPICAL ANTIPSYCHOTICS

Produktu pārskats:

Active ingredient group (AIG) number: 0122583003; AHFS:

Autorizācija statuss:

APPROVED

Autorizācija datums:

2016-11-08

Produkta apraksts

                                _AA-CLOZAPINE (Clozapine Tablets)_
_ _
_ _
_Page 1 of 55 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
AA-CLOZAPINE
Clozapine Tablets
Tablets, 25 mg, 50 mg, 100 mg and 200 mg, oral
USP
Antipsychotic Agent
AA PHARMA INC.
1165 Creditstone Road, Unit #1
Vaughan, Ontario
L4K 4N7
Date of Initial Authorization:
AUG 19, 2016
Date of Revision:
APRIL 03, 2023
Submission Control Number: 269276
_AA-CLOZAPINE (Clozapine Tablets)_
_ _
_ _
_Page 2 of 55 _
RECENT MAJOR LABEL CHANGES
7 WARNINGS AND PRECAUTIONS, Skin
04/2023
7 WARNINGS AND PRECAUTIONS, 7.1.4 Geriatrics
04/2023
7 WARNINGS AND PRECAUTIONS, General, Anticholinergic Activity
04/2023
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
RECENT MAJOR LABEL CHANGES
................................................................................................
2
TABLE OF CONTENTS
..................................................................................................................
2
1 INDICATIONS
...........................................................................................................................
4
1.1 Pediatrics
...............................................................................................................................
5
1.2 Geriatrics
...............................................................................................................................
5
2 CONTRAINDICATIONS
..............................................................................................................
5
3 SERIOUS WARNINGS AND PRECAUTIONS BOX
.........................................................................
6
4 DOSAGE AND ADMINISTRATION
..............................................................................................
6
4.1 Dosing Considerations
...........................................................................................................
6
4.2 Recommended Dose and Dosage Adjustment
.......................................
                                
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Produkta apraksts Produkta apraksts franču 03-04-2023

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