TARO-IMIPENEM-CILASTATIN POWDER FOR SOLUTION

Maa: Kanada

Kieli: englanti

Lähde: Health Canada

Aktiivinen ainesosa:

IMIPENEM; CILASTATIN (CILASTATIN SODIUM)

Saatavilla:

SUN PHARMA CANADA INC

ATC-koodi:

J01DH51

INN (Kansainvälinen yleisnimi):

IMIPENEM AND CILASTATIN

Annos:

250MG; 250MG

Lääkemuoto:

POWDER FOR SOLUTION

Koostumus:

IMIPENEM 250MG; CILASTATIN (CILASTATIN SODIUM) 250MG

Antoreitti:

INTRAVENOUS

Kpl paketissa:

30ML

Prescription tyyppi:

Prescription

Terapeuttinen alue:

CARBAPENEMS

Tuoteyhteenveto:

Active ingredient group (AIG) number: 0218820002; AHFS:

Valtuutuksen tilan:

APPROVED

Valtuutus päivämäärä:

2021-01-19

Valmisteyhteenveto

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_TARO-Imipenem-Cilastatin (Imipenem and Cilastatin for Injection, USP)
Page 1 of 57 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
TARO-IMIPENEM-CILASTATIN
Imipenem and Cilastatin for Injection
250 mg imipenem and 250 mg cilastatin (as cilastatin sodium) per vial
500 mg imipenem and 500 mg cilastatin (as cilastatin sodium) per vial
Sterile powder for solution, I.V. Infusion
USP
ANTIBIOTIC
Sun Pharma Canada Inc.,
126 East Drive
Brampton, ON
L6T 1C1
Date of Initial Authorization:
MAY 20, 2010
Date of Revision:
JULY 22, 2022
Submission Control Number: 260927
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_TARO-Imipenem-Cilastatin (Imipenem and Cilastatin for Injection, USP)
Page 2 of 57 _
RECENT MAJOR LABEL CHANGES
4. DOSAGE AND ADMINISTRATION
07/2022
7. WARNINGS AND PRECAUTIONS
01/2021
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
RECENT MAJOR LABEL
CHANGES.............................................................................................
2
TABLE OF CONTENTS
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2
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................................
4
1
INDICATIONS........................................................................................................................
4
1.1 PEDIATRICS
..........................................................................................................................
5
1.2 GERIATRICS
..........................................................................................................................
5
2 CONTRAINDICATIONS
..........................................................................................................
5
3 SERIOUS WARNINGS AND PRECAUTIONS
BOX......................................................................
5
4 DOSAGE AND ADMINISTRATION
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6
4.