FOSMICIN SERBUK INJEKSI 2 G/VIAL

Negara: Indonesia

Bahasa: Bahasa Indonesia

Sumber: Badan Pengawas Obat dan Makanan RI - Indonesian Food and Drug Supervisory Agency

Karakteristik produk Karakteristik produk (SPC)
31-12-2021

Bahan aktif:

FOSFOMYCIN SODIUM

Tersedia dari:

MEIJI - Indonesia

INN (Nama Internasional):

FOSFOMYCIN SODIUM

Dosis:

2 G/VIAL

Bentuk farmasi:

SERBUK INJEKSI

Unit dalam paket:

DUS, 10 VIAL @ 2 G

Diproduksi oleh:

MEIJI - Indonesia

Tanggal Otorisasi:

2015-09-23

Karakteristik produk

                                1 g (Potency) of fosfomycin sodium
each vial contains
FOSMICIN for Injection
_Pseudomonas aeruginosa,_
_Proteus sp.,_
_Serratia_
_marcescens_
and multi-drug resistant
strains of _Staphylococcus_
_aureus _and _E. coli._
.
Composition
*
1 g / vial :
(Potency) of fosfomycin sodium
20 mg (Potency)/ml (Distilled
water for Injection)
50 mg (Potency)/ml (Distilled
water for Injection)
20 mg (Potency)/ml
(5 % Glucose solution)
50 mg (Potency)/ml
(5 % Glucose solution)
The usual daily dosage of FOSMICIN FOR I.V. USE is
2 to 4 g (Potency) for adults and 100 to 200 mg (Potency)/kg for
children;
both of these a
Intravenous Drip Infusion
FOSMICIN 1 g, Reg. No. DKL9715302444A1
FOSMICIN 2 g, Reg. No. DKL9715302444B1
(Print code)
Licensed by
Meiji Seika Pharma Co., Ltd.
Tokyo, Japan
PT MEIJI INDONESIAN
PHARMACEUTICAL INDUSTRIES
BANGIL - PASURUAN, JAWA TIMUR - INDONESIA
per g (Potency) ; accordingly, care should be taken when
ontains 14.5 mEq of sodium
The safety of this drug for administration during the course
of pregnancy has not yet been established. Therefore, it is
desirable to avoid the use of this drug in females who are,
or may be pregnant.
_Pseudomonas aeruginosa_,_ Proteus sp._, _Serratia marcescens_, and
inhibit
HARUS DENGAN RESEP DOKTER
STORAGE CONDITION
Nama Produk
®
Brosur Fosmicin
Tanggal Desain
Keterangan
Ukuran
220 x 270 mm
- 15 Desember 2021
- 05 Maret 2012
- Perubahan suhu penyimpanan
- Perubahan logo Meiji dan nama lisensor
Bahan
HVS 60 g
Warna
Black
Store below 30°C and the drug should be used before expiration
date stated on the label. After reconstitution, the solution stable
at 30±2°C and 5±3°C for 24 hours.
DISETUJUI OLEH BPOM: 20/12/2021
ID: EREG100253VR12000118
EREG100253VR12100011
                                
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