PLATINUM MUSCLE AND BACK PAIN RELIEF TABLET

Ország: Kanada

Nyelv: angol

Forrás: Health Canada

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Termékjellemzők Termékjellemzők (SPC)
24-01-2011

Aktív összetevők:

METHOCARBAMOL; IBUPROFEN

Beszerezhető a:

VITA HEALTH PRODUCTS INC

ATC-kód:

M03BA53

INN (nemzetközi neve):

METHOCARBAMOL, COMBINATIONS EXCL PSYCHOLEPTICS

Adagolás:

500MG; 200MG

Gyógyszerészeti forma:

TABLET

Összetétel:

METHOCARBAMOL 500MG; IBUPROFEN 200MG

Az alkalmazás módja:

ORAL

db csomag:

18/27/40/50/80

Recept típusa:

OTC

Terápiás terület:

OTHER NONSTEROIDAL ANTIIMFLAMMATORY AGENTS

Termék összefoglaló:

Active ingredient group (AIG) number: 0248961001; AHFS:

Engedélyezési státusz:

APPROVED

Engedély dátuma:

2011-01-20

Termékjellemzők

                                PRODUCT MONOGRAPH
PLATINUM MUSCLE AND BACK PAIN RELIEF
500 MG METHOCARBAMOL AND 200 MG IBUPROFEN CAPLETS
THERAPEUTIC CLASSIFICATION
MUSCLE RELAXANT / ANALGESIC
VITA HEALTH PRODUCTS INC.
DATE OF PREPARATION:
150 BEGHIN AVENUE,
January 17, 2011
WINNIPEG, MB
CANADA, R2J 3W2
CONTROL NO.: 128349
2
TABLE OF CONTENTS
Page
CLINICAL
PHARMACOLOGY.............................................................................................3
INDICATIONS:
...............................................................................................................6
CONTRAINDICATIONS
.....................................................................................................6
WARNINGS:
.................................................................................................................7
PRECAUTIONS
.............................................................................................................10
DRUG INTERACTIONS
...................................................................................................12
ADVERSE
REACTIONS..................................................................................................13
SYMPTOMS AND TREATMENT OF OVERDOSE
...............................................................15
DOSAGE AND
ADMINISTRATION...................................................................................16
PHARMACEUTICAL
INFORMATION.................................................................................16
COMPOSITION
............................................................................................................19
AVAILABILITY OF DOSAGE
FORMS................................................................................19
INFORMATION FOR THE CONSUMER
.............................................................................20
PHARMACOLOGY
..............................................................................................22
CLINICAL TRIALS
..........................................................................................
                                
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