Daptomycin Hospira

Negara: Uni Eropa

Bahasa: Inggris

Sumber: EMA (European Medicines Agency)

Beli Sekarang

Selebaran informasi Selebaran informasi (PIL)
06-04-2022
Karakteristik produk Karakteristik produk (SPC)
06-04-2022

Bahan aktif:

daptomycin

Tersedia dari:

Pfizer Europe MA EEIG

Kode ATC:

J01XX09

INN (Nama Internasional):

daptomycin

Kelompok Terapi:

Antibacterials for systemic use,

Area terapi:

Soft Tissue Infections; Skin Diseases, Bacterial

Indikasi Terapi:

Daptomycin is indicated for the treatment of the following infections.Adult and paediatric (1 to 17 years of age) patients with complicated skin and soft-tissue infections (cSSTI).Adult patients with right-sided infective endocarditis (RIE) due to Staphylococcus aureus. It isrecommended that the decision to use daptomycin should take into account the antibacterial susceptibility of the organism and should be based on expert advice.Adult and paediatric (1 to 17 years of age) patients with Staphylococcus aureus bacteraemia (SAB).In adults, use in bacteraemia should be associated with RIE or with cSSTI, while in paediatric patients, use in bacteraemia should be associated with cSSTI.Daptomycin is active against Gram positive bacteria only. In mixed infections where Gram negative and/or certain types of anaerobic bacteria are suspected, daptomycin should be co-administered with appropriate antibacterial agent(s).Consideration should be given to official guidance on the appropriate use of antibacterial agents.

Ringkasan produk:

Revision: 13

Status otorisasi:

Authorised

Tanggal Otorisasi:

2017-03-22

Selebaran informasi

                                38
B. PACKAGE LEAFLET
39
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
DAPTOMYCIN HOSPIRA 350 MG POWDER FOR SOLUTION FOR INJECTION/INFUSION
daptomycin
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START USING THIS
MEDICINE BECAUSE IT CONTAINS IMPORTANT
INFORMATION FOR YOU.
-
Keep this leaflet. You may need to read it again.
-
If you have any further questions, ask your doctor or nurse.
-
This medicine has been prescribed for you only. Do not pass it on to
others. It may harm them, even
if their signs of illness are the same as yours.
-
If you get any side effects, talk to your doctor or nurse. This
includes any possible side effects not
listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Daptomycin Hospira is and what it is used for
2.
What you need to know before you are given Daptomycin Hospira
3.
How Daptomycin Hospira is given
4.
Possible side effects
5.
How to store Daptomycin Hospira
6.
Contents of the pack and other information
1.
WHAT DAPTOMYCIN HOSPIRA IS AND WHAT IT IS USED FOR
The active substance in Daptomycin Hospira powder for solution for
injection/infusion is daptomycin.
Daptomycin is an antibacterial that can stop the growth of certain
bacteria. Daptomycin Hospira is used in
adults and in children and adolescents (age from 1 to 17 years) to
treat infections of the skin and the
tissues below the skin. It is also used to treat infections in the
blood when associated with skin infection.
Daptomycin Hospira is also used in adults to treat infections in the
tissues that line the inside of the heart
(including heart valves) which are caused by a type of bacteria called
_Staphylococcus aureus._
It is also
used to treat infections in the blood caused by the same type of
bacteria when associated with heart
infection.
Depending on the type of infection(s) that you have, your doctor may
also prescribe other antibacterials
while you are receiving treatment with Daptomycin Hospira.
2.
WHAT YOU NEED TO KNOW BEFORE YOU ARE GIVEN DAPTOMYCIN HOSPIRA
YOU SHOULD NOT BE GIVEN DAPTOMYCIN HOSPIRA
If 
                                
                                Baca dokumen lengkapnya
                                
                            

Karakteristik produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Daptomycin Hospira 350 mg powder for solution for injection/infusion
Daptomycin Hospira 500 mg powder for solution for injection/infusion
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Daptomycin Hospira 350 mg powder for solution for injection/infusion
Each vial contains 350 mg daptomycin.
One mL provides 50 mg of daptomycin after reconstitution with 7 mL of
sodium chloride 9 mg/mL
(0.9%) solution for injection.
Daptomycin Hospira 500 mg powder for solution for injection/infusion
Each vial contains 500 mg daptomycin.
One mL provides 50 mg of daptomycin after reconstitution with 10 mL of
sodium chloride 9 mg/mL
(0.9%) solution for injection.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Daptomycin Hospira 350 mg powder for solution for injection/infusion
Powder for solution for injection/infusion.
A light yellow to light brown lyophilised cake or powder.
Daptomycin Hospira 500 mg powder for solution for injection/infusion
Powder for solution for injection/infusion.
A light yellow to light brown lyophilised cake or powder.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Daptomycin is indicated for the treatment of the following infections
(see sections 4.4 and 5.1).
-
Adult and paediatric (1 to 17 years of age) patients with complicated
skin and soft-tissue infections
(cSSTI).
-
Adult patients with right-sided infective endocarditis (RIE) due to
_Staphylococcus aureus. _
It is
recommended that the decision to use daptomycin should take into
account the antibacterial
susceptibility of the organism and should be based on expert advice
(see sections 4.4 and 5.1).
-
Adult and paediatric (1 to 17 years of age) patients with
_ Staphylococcus aureus _
bacteraemia (SAB).
In adults, use in bacteraemia should be associated with RIE or with
cSSTI, while in paediatric
patients, use in bacteraemia should be associated with cSSTI.
3
Daptomycin is active against Gram positive bacteria only (see section
5.1). In mixed infec
                                
                                Baca dokumen lengkapnya
                                
                            

Dokumen dalam bahasa lain

Selebaran informasi Selebaran informasi Bulgar 06-04-2022
Karakteristik produk Karakteristik produk Bulgar 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Bulgar 18-04-2018
Selebaran informasi Selebaran informasi Spanyol 06-04-2022
Karakteristik produk Karakteristik produk Spanyol 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Spanyol 18-04-2018
Selebaran informasi Selebaran informasi Cheska 06-04-2022
Karakteristik produk Karakteristik produk Cheska 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Cheska 18-04-2018
Selebaran informasi Selebaran informasi Dansk 06-04-2022
Karakteristik produk Karakteristik produk Dansk 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Dansk 18-04-2018
Selebaran informasi Selebaran informasi Jerman 06-04-2022
Karakteristik produk Karakteristik produk Jerman 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Jerman 18-04-2018
Selebaran informasi Selebaran informasi Esti 06-04-2022
Karakteristik produk Karakteristik produk Esti 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Esti 18-04-2018
Selebaran informasi Selebaran informasi Yunani 06-04-2022
Karakteristik produk Karakteristik produk Yunani 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Yunani 18-04-2018
Selebaran informasi Selebaran informasi Prancis 06-04-2022
Karakteristik produk Karakteristik produk Prancis 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Prancis 18-04-2018
Selebaran informasi Selebaran informasi Italia 06-04-2022
Karakteristik produk Karakteristik produk Italia 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Italia 18-04-2018
Selebaran informasi Selebaran informasi Latvi 06-04-2022
Karakteristik produk Karakteristik produk Latvi 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Latvi 18-04-2018
Selebaran informasi Selebaran informasi Lituavi 06-04-2022
Karakteristik produk Karakteristik produk Lituavi 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Lituavi 18-04-2018
Selebaran informasi Selebaran informasi Hungaria 06-04-2022
Karakteristik produk Karakteristik produk Hungaria 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Hungaria 18-04-2018
Selebaran informasi Selebaran informasi Malta 06-04-2022
Karakteristik produk Karakteristik produk Malta 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Malta 18-04-2018
Selebaran informasi Selebaran informasi Belanda 06-04-2022
Karakteristik produk Karakteristik produk Belanda 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Belanda 18-04-2018
Selebaran informasi Selebaran informasi Polski 06-04-2022
Karakteristik produk Karakteristik produk Polski 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Polski 18-04-2018
Selebaran informasi Selebaran informasi Portugis 06-04-2022
Karakteristik produk Karakteristik produk Portugis 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Portugis 18-04-2018
Selebaran informasi Selebaran informasi Rumania 06-04-2022
Karakteristik produk Karakteristik produk Rumania 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Rumania 18-04-2018
Selebaran informasi Selebaran informasi Slovak 06-04-2022
Karakteristik produk Karakteristik produk Slovak 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Slovak 18-04-2018
Selebaran informasi Selebaran informasi Sloven 06-04-2022
Karakteristik produk Karakteristik produk Sloven 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Sloven 18-04-2018
Selebaran informasi Selebaran informasi Suomi 06-04-2022
Karakteristik produk Karakteristik produk Suomi 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Suomi 18-04-2018
Selebaran informasi Selebaran informasi Swedia 06-04-2022
Karakteristik produk Karakteristik produk Swedia 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Swedia 18-04-2018
Selebaran informasi Selebaran informasi Norwegia 06-04-2022
Karakteristik produk Karakteristik produk Norwegia 06-04-2022
Selebaran informasi Selebaran informasi Islandia 06-04-2022
Karakteristik produk Karakteristik produk Islandia 06-04-2022
Selebaran informasi Selebaran informasi Kroasia 06-04-2022
Karakteristik produk Karakteristik produk Kroasia 06-04-2022
Laporan Penilaian publik Laporan Penilaian publik Kroasia 18-04-2018

Peringatan pencarian terkait dengan produk ini