PLATINUM MUSCLE AND BACK PAIN RELIEF TABLET

Država: Kanada

Jezik: angleščina

Source: Health Canada

Kupite ga zdaj

Prenos Lastnosti izdelka (SPC)
24-01-2011

Aktivna sestavina:

METHOCARBAMOL; IBUPROFEN

Dostopno od:

VITA HEALTH PRODUCTS INC

Koda artikla:

M03BA53

INN (mednarodno ime):

METHOCARBAMOL, COMBINATIONS EXCL PSYCHOLEPTICS

Odmerek:

500MG; 200MG

Farmacevtska oblika:

TABLET

Sestava:

METHOCARBAMOL 500MG; IBUPROFEN 200MG

Pot uporabe:

ORAL

Enote v paketu:

18/27/40/50/80

Tip zastaranja:

OTC

Terapevtsko območje:

OTHER NONSTEROIDAL ANTIIMFLAMMATORY AGENTS

Povzetek izdelek:

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

Status dovoljenje:

APPROVED

Datum dovoljenje:

2011-01-20

Lastnosti izdelka

                                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
..........................................................................................
                                
                                Preberite celoten dokument
                                
                            

Dokumenti v drugih jezikih

Lastnosti izdelka Lastnosti izdelka francoščina 17-01-2011