THALOMID CAPSULE

Negara: Kanada

Bahasa: Inggris

Sumber: Health Canada

Beli Sekarang

Unduh Karakteristik produk (SPC)
01-03-2024

Bahan aktif:

THALIDOMIDE

Tersedia dari:

CELGENE INC

Kode ATC:

L04AX02

INN (Nama Internasional):

THALIDOMIDE

Dosis:

200MG

Bentuk farmasi:

CAPSULE

Komposisi:

THALIDOMIDE 200MG

Rute administrasi :

ORAL

Unit dalam paket:

28

Jenis Resep:

Prescription

Area terapi:

Immunomodulatory Agents

Ringkasan produk:

Active ingredient group (AIG) number: 0152770004; AHFS:

Status otorisasi:

APPROVED

Tanggal Otorisasi:

2010-08-04

Karakteristik produk

                                _ _
_ _
_Page 1 of 53_
PRODUCT MONOGRAPH
Pr
THALOMID
®
Thalidomide Capsules
House Standard
50 mg, 100 mg, 200 mg
Immunomodulatory Agent
SUBMISSION CONTROL NO: 283297
®
THALOMID is a registered trademark of Celgene Corporation used under
license by Bristol-Myers Squibb
Canada.
Bristol-Myers Squibb Canada
2344 Alfred-Nobel Blvd
Suite 300
Saint-Laurent, QC
H4S 0A4
DATE OF INITIAL AUTHORIZATION:
MAR 01, 2024
_ _
_ _
_Page 2 of 53_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL
INFORMATION................................................................3
SUMMARY PRODUCT INFORMATION
....................................................................................3
INDICATIONS AND CLINICAL USE
..........................................................................................3
CONTRAINDICATIONS
...............................................................................................................5
WARNINGS AND PRECAUTIONS
..............................................................................................5
ADVERSE REACTIONS
..............................................................................................................15
DRUG INTERACTIONS
..............................................................................................................23
DOSAGE AND ADMINISTRATION
..........................................................................................25
OVERDOSAGE
............................................................................................................................29
ACTION AND CLINICAL PHARMACOLOGY
........................................................................30
STORAGE AND STABILITY
......................................................................................................33
SPECIAL HANDLING INSTRUCTIONS
...................................................................................33
DOSAGE FORMS, COMPOSITION AND PACKAGING
.........................................................33
PART II: SCIENTIFIC INFORMATION
...
                                
                                Baca dokumen lengkapnya
                                
                            

Dokumen dalam bahasa lain

Karakteristik produk Karakteristik produk Prancis 01-03-2024

Peringatan pencarian terkait dengan produk ini