PMS-PIROXICAM SUPPOSITORIES -20MG SUPPOSITORY

Country: Kanada

Tungumál: enska

Heimild: Health Canada

Kauptu það núna

Vara einkenni Vara einkenni (SPC)
01-03-2010

Virkt innihaldsefni:

PIROXICAM

Fáanlegur frá:

PHARMASCIENCE INC

ATC númer:

M01AC01

INN (Alþjóðlegt nafn):

PIROXICAM

Skammtar:

20MG

Lyfjaform:

SUPPOSITORY

Samsetning:

PIROXICAM 20MG

Stjórnsýsluleið:

RECTAL

Einingar í pakka:

30 SUPPOSITORIES

Gerð lyfseðils:

Prescription

Lækningarsvæði:

OTHER NONSTEROIDAL ANTIIMFLAMMATORY AGENTS

Vörulýsing:

Active ingredient group (AIG) number: 0114612001; AHFS:

Leyfisstaða:

CANCELLED POST MARKET

Leyfisdagur:

2016-10-28

Vara einkenni

                                PRODUCT MONOGRAPH
Pr
pms-PIROXICAM
Piroxicam, USP
10 mg and 20 mg Capsules
10 mg and 20 mg Suppositories
Nonsteroidal Anti-Inflammatory Drug (NSAID)
PHARMASCIENCE INC.
DATE OF REVISION:
6111 Royalmount Avenue
February 17, 2010
Montreal, Quebec
H4P 2T4
CONTROL # 131400
_ _
2
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL
INFORMATION..........................................................3
SUMMARY PRODUCT INFORMATION
.......................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................4
WARNINGS AND
PRECAUTIONS..................................................................................5
ADVERSE
REACTIONS..................................................................................................14
DRUG INTERACTIONS
.................................................................................................19
DOSAGE AND ADMINISTRATION
..............................................................................22
OVERDOSAGE
................................................................................................................23
ACTION AND CLINICAL
PHARMACOLOGY.............................................................23
STORAGE AND
STABILITY..........................................................................................24
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................24
PART II: SCIENTIFIC INFORMATION
................................................................................26
PHARMACEUTICAL
INFORMATION..........................................................................26
CLINICAL TRIALS
..........................................................................................................27
DETAILED PHARMACOLOGY
.....................................................................................27

                                
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