Cefepime-Asteria Inj. 1g powder for solution for injection

Quốc gia: Armenia

Ngôn ngữ: Tiếng Anh

Nguồn: Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

Download Tờ rơi thông tin (PIL)
18-03-2021

Thành phần hoạt chất:

cefepime (cefepime hydrochloride)

Sẵn có từ:

Hankook Korus Pharm Co.

Mã ATC:

J01DE01

INN (Tên quốc tế):

cefepime (cefepime hydrochloride)

Liều dùng:

1000mg

Dạng dược phẩm:

powder for solution for injection

Các đơn vị trong gói:

(1) and (10) glass vial

Loại thuốc theo toa:

Prescription

Tình trạng ủy quyền:

Registered

Ngày ủy quyền:

2020-07-23

Tờ rơi thông tin

                                To be prescribed
ATC Code : J01DE01
Fourth-generation cephalosporin
CEFEPIME-ASTERIA
INJ. 1G
Cefepime HCI 1g
POWDER FOR SOLUTION FOR INJECTION
[COMPOSITION]
1 VIAL CONTAINS
CEFEPIME
HCL---------------------------------------------------------------------------------------------------------------------1G
(POTENCY)
EXCIPIENTS : L-ARGININE
DESCRIPTION
White to yellowish crystalline powder in clear vials
INDICATIONS
Cefepime-Asteria is indicated in the treatment of infections caused by
bacteria that are cefepime-sensitive:
- lower respiratory tract infections, including nosocomial pneumonia
and community acquired pneumonia, acute
bacterial exacerbation of chronic bronchitis and secondary bacterial
infection of acute bronchitis;
- uncomplicated and complicated urinary tract infections, including
pyelonephritis;
- skin and subcutaneous infections;
- intra-abdominal infections, including peritonitis and biliary tract
infections;
- gynaecological infections;
- bacterial meningitis in infants and children;
- In combination with other antibacterial agents in the management of
neutropenic patients with fever that is
suspected to be due to a bacterial infection;
- Treatment of patients with bacteraemia that occurs in association
with, or is suspected to be associated with, any of
the infections listed above.
Consideration should be given to official guidance on the appropriate
use of antibacterial agents.
DOSAGE AND ADMINISTRATION
Cefepime-Asteria can be administered via intravenous use or
intramuscular use.
After reconstitution, the solution is yellow to yellow-brown.
The usual dose and the route of administration vary in accordance with
the severity of the infection, the renal
function and the general conditions of the patient.
The IV route of administration is preferable in the patients with
severe infections or in a life-threatening situation,
particularly if there is the possibility of shock.
Adults and children weighing > 40 kg with normal renal function:
SEVERITY OF THE INFECTION
DOSAGE AND ROUTE OF ADMINISTRATION
INT
                                
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Đặc tính sản phẩm

                                SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF THE MEDICINAL PRODUCT
Cefepime-Asteria Inj. 1g
2. QUALITATIVE AND QUANTITATIVE COMPOSITION
Active ingredient
No.
Chemical
Name
Quantity/vial
Use
1
_ _
Cefepime
Hydrochloride
1g
(potency)
Active
ingredient
_ _
Excipients
No.
Chemical
Name
Quantity/vial
Use
1
_ _
L-arginine
q.s.
pH
Adjuster
_ _ 3. PHARMACEUTICAL FORM
Powder for solution for injection
3.1 DESCRIPTION
White to yellowish crystalline powder in clear vials
4. CLINICAL PARTICULARS
4.1 THERAPEUTIC INDICATIONS
Cefepime-Asteria is indicated in the treatment of infections caused by
bacteria that are cefepime-sensitive:
- lower respiratory tract infections, including nosocomial pneumonia
and community acquired pneumonia, acute
bacterial exacerbation of chronic bronchitis and secondary bacterial
infection of acute bronchitis;
- uncomplicated and complicated urinary tract infections, including
pyelonephritis;
- skin and subcutaneous infections;
- intra-abdominal infections, including peritonitis and biliary tract
infections;
- gynaecological infections;
- bacterial meningitis in infants and children;
- In combination with other antibacterial agents in the management of
neutropenic patients with fever that is
suspected to be due to a bacterial infection;
- Treatment of patients with bacteraemia that occurs in association
with, or is suspected to be associated with, any of
the infections listed above.
Consideration should be given to official guidance on the appropriate
use of antibacterial agents.
4.2 POSOLOGY AND METHOD OF ADMINISTRATION
Cefepime-Asteria can be administered via intravenous use or
intramuscular use.
After reconstitution, the solution is yellow to yellow-brown.
The usual dose and the route of administration vary in accordance with
the severity of the infection, the renal
function and the general conditions of the patient.
The IV route of administration is preferable in the patients with
severe infections or in a life-threatening situation,
particularly if there is the possibility of shock.
Adults and 
                                
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