CIPRO TABLET

Krajina: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Aktívna zložka:

CIPROFLOXACIN (CIPROFLOXACIN HYDROCHLORIDE)

Dostupné z:

BAYER INC

ATC kód:

J01MA02

INN (Medzinárodný Name):

CIPROFLOXACIN

Dávkovanie:

750MG

Forma lieku:

TABLET

Zloženie:

CIPROFLOXACIN (CIPROFLOXACIN HYDROCHLORIDE) 750MG

Spôsob podávania:

ORAL

Počet v balení:

50/100

Typ predpisu:

Prescription

Terapeutické oblasti:

QUINOLONES

Prehľad produktov:

Active ingredient group (AIG) number: 0123207002; AHFS:

Stav Autorizácia:

CANCELLED POST MARKET

Dátum Autorizácia:

2018-12-10

Súhrn charakteristických

_CIPRO_
_®_
_ and CIPRO_
®
_ ORAL SUSPENSION_
Page 1 of 58
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
CIPRO
®
(Ciprofloxacin tablet USP)
250 mg, 500 mg, 750 mg
PR
CIPRO
® ORAL SUSPENSION
(Ciprofloxacin oral suspension)
10 g/100 mL
Antibacterial Agent
Manufactured by:
Bayer Inc.
2920 Matheson Boulevard East
Mississauga, Ontario
L4W 5R6
www.bayer.ca
Date of Revision:
February 18, 2020
Submission Control No: 233351
© 2020, Bayer Inc.
® TM see www.bayer.ca/tm-mc
All other trademarks are the property of their respective owners.
_CIPRO_
_®_
_ and CIPRO_
®
_ ORAL SUSPENSION_
Page 2 of 58
TABLE OF CONTENTS
PART
I:
HEALTH
PROFESSIONAL
INFORMATION ..........................................................
3
SUMMARY PRODUCT INFORMATION
...................................................................................
3
INDICATIONS AND CLINICAL USE
.........................................................................................
3
CONTRAINDICATIONS
..............................................................................................................
7
WARNINGS AND PRECAUTIONS
.............................................................................................
8
ADVERSE REACTIONS
.............................................................................................................
14
DRUG INTERACTIONS
.............................................................................................................
17
DOSAGE AND ADMINISTRATION
.........................................................................................
22
OVERDOSAGE
...........................................................................................................................
25
ACTION AND CLINICAL PHARMACOLOGY
.......................................................................
26
STORAGE AND STABILITY
.....................................................................................................
28
DOSAGE FORMS, COMPOSITION AND PACKAGING
.................................