DOM-CIPROFLOXACIN TABLET

Ország: Kanada

Nyelv: angol

Forrás: Health Canada

Aktív összetevők:

CIPROFLOXACIN (CIPROFLOXACIN HYDROCHLORIDE)

Beszerezhető a:

DOMINION PHARMACAL

ATC-kód:

J01MA02

INN (nemzetközi neve):

CIPROFLOXACIN

Adagolás:

750MG

Gyógyszerészeti forma:

TABLET

Összetétel:

CIPROFLOXACIN (CIPROFLOXACIN HYDROCHLORIDE) 750MG

Az alkalmazás módja:

ORAL

db csomag:

50/100

Recept típusa:

Prescription

Terápiás terület:

QUINOLONES

Termék összefoglaló:

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

Engedélyezési státusz:

APPROVED

Engedély dátuma:

2004-03-24

Termékjellemzők

PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
DOM-CIPROFLOXACIN
(Ciprofloxacin Hydrochloride Tablets, USP)
100 mg, 250 mg, 500 mg and 750 mg
ANTIBACTERIAL AGENT
DOMINION PHARMACAL
6111 Royalmount Ave., Suite 100,
Montréal, Quebec
H4P 2T4 DATE OF REVISION: SEPTEMBER 10, 2019
SUBMISSION CONTROL NO.: 229111
_Dom-CIPROFLOXACIN Product Monograph _
_Page 2 of 49_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
............................................................ 3
SUMMARY PRODUCT INFORMATION
..................................................................................
3
INDICATIONS AND CLINICAL USE
........................................................................................
3
CONTRAINDICATIONS
.............................................................................................................
6
WARNINGS AND PRECAUTIONS
............................................................................................
6
ADVERSE REACTIONS
............................................................................................................
11
DRUG INTERACTIONS
............................................................................................................
14
DOSAGE AND ADMINISTRATION
........................................................................................
19
OVERDOSAGE
...........................................................................................................................
21
ACTION AND CLINICAL PHARMACOLOGY
......................................................................
21
STORAGE AND STABILITY
....................................................................................................
23
DOSAGE FORMS, COMPOSITION AND PACKAGING
....................................................... 23
PART II: SCIENTIFIC INFORMATION
..................................................................................
25
PHARMACEUTICAL INFORMATION
..........................................................................