EPIRUBICIN HYDROCHLORIDE INJECTION SOLUTION

Nchi: Kanada

Lugha: Kiingereza

Chanzo: Health Canada

Nunua Sasa

Shusha Tabia za bidhaa (SPC)
24-07-2013

Viambatanisho vya kazi:

EPIRUBICIN HYDROCHLORIDE

Inapatikana kutoka:

OMEGA LABORATORIES LIMITED

ATC kanuni:

L01DB03

INN (Jina la Kimataifa):

EPIRUBICIN

Kipimo:

2MG

Dawa fomu:

SOLUTION

Tungo:

EPIRUBICIN HYDROCHLORIDE 2MG

Njia ya uendeshaji:

INTRAVENOUS

Vitengo katika mfuko:

5/25/100ML

Dawa ya aina:

Prescription

Eneo la matibabu:

ANTINEOPLASTIC AGENTS

Bidhaa muhtasari:

Active ingredient group (AIG) number: 0116901002; AHFS:

Idhini hali ya:

APPROVED

Idhini ya tarehe:

2013-07-23

Tabia za bidhaa

                                PRODUCT MONOGRAPH
PR
E
PIRUBICIN
H
YDROCHLORIDE
I
NJECTION
2 mg/mL
Professed Standard
ANTINEOPLASTIC AGENT
Omega Laboratories Limited
11,177 Hamon Street
Montreal, Quebec
H3M 3E4
SUBMISSION CONTROL NO.: 141753
DATE OF PREPARATION:
July 15, 2013
_ _
IMPORTANT: PLEASE READ
E
PIRUBICIN
H
YDROCHLORIDE
I
NJECTION
Product Monograph
Page
2
of
38
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
................................................................. 3
SUMMARY PRODUCT INFORMATION
.......................................................................................
3
INDICATIONS AND CLINICAL USE
............................................................................................
3
CONTRAINDICATIONS
..................................................................................................................
4
WARNINGS AND PRECAUTIONS
................................................................................................
4
ADVERSE REACTIONS
..................................................................................................................
9
DRUG INTERACTIONS
................................................................................................................
14
DOSAGE AND ADMINISTRATION
............................................................................................
14
OVERDOSAGE
...............................................................................................................................
17
ACTION AND CLINICAL PHARMACOLOGY
...........................................................................
17
STORAGE AND STABILITY
........................................................................................................
19
SPECIAL HANDLING INSTRUCTIONS
......................................................................................
19
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................................ 20
PART II: SCIENTIFIC INFORMATION
.................................................
                                
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