Caspofungin Accord

Negara: Uni Eropa

Bahasa: Inggris

Sumber: EMA (European Medicines Agency)

Beli Sekarang

Selebaran informasi Selebaran informasi (PIL)
05-03-2020
Karakteristik produk Karakteristik produk (SPC)
05-03-2020

Bahan aktif:

caspofungin acetate

Tersedia dari:

Accord Healthcare S.L.U.

Kode ATC:

J02AX04

INN (Nama Internasional):

caspofungin

Kelompok Terapi:

Antimycotics for systemic use

Area terapi:

Candidiasis; Aspergillosis

Indikasi Terapi:

Treatment of invasive candidiasis in adult or paediatric patients.Treatment of invasive aspergillosis in adult or paediatric patients who are refractory to or intolerant of amphotericin B, lipid formulations of amphotericin B and/or itraconazole. Refractoriness is defined as progression of infection or failure to improve after a minimum of 7 days of prior therapeutic doses of effective antifungal therapy.Empirical therapy for presumed fungal infections (such as Candida or Aspergillus) in febrile, neutropaenic adult or paediatric patients.

Ringkasan produk:

Revision: 6

Status otorisasi:

Withdrawn

Tanggal Otorisasi:

2016-02-11

Selebaran informasi

                                30
B. PACKAGE LEAFLET
31
PACKAGE LEAFLET: INFORMATION FOR THE USER
CASPOFUNGIN ACCORD 50 MG POWDER FOR CONCENTRATE FOR SOLUTION FOR
INFUSION
CASPOFUNGIN ACCORD 70 MG POWDER FOR CONCENTRATE FOR SOLUTION FOR
INFUSION
caspofungin
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU OR YOUR CHILD ARE GIVEN
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, nurse or
pharmacist.

If you get any side effects, talk to your doctor, nurse or pharmacist.
This includes any possible
side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Caspofungin Accord is and what it is used for
2.
What you need to know before you are given Caspofungin Accord
3.
How to use Caspofungin Accord
4.
Possible side effects
5.
How to store Caspofungin Accord
6.
Contents of the pack and other information
1.
WHAT CASPOFUNGIN ACCORD IS AND WHAT IT IS USED FOR
WHAT CASPOFUNGIN ACCORD IS
Caspofungin Accord contains a medicine called caspofungin. This
belongs to a group of medicines
called anti-fungals.
WHAT CASPOFUNGIN ACCORD IS USED FOR
Caspofungin Accord is used to treat the following infections in
children, adolescents and adults:

serious fungal infections in your tissues or organs (called
‘invasive candidiasis’). This infection
is caused by fungal (yeast) cells called Candida.
People who might get this type of infection include those who have
just had an operation or
those whose immune systems are weak. Fever and chills that do not
respond to an antibiotic are
the most common signs of this type of infection.

fungal infections in your nose, nasal sinuses or lungs (called
‘invasive aspergillosis’) if other
anti-fungal treatments have not worked or have caused side effects.
This infection is caused by a
mould called Aspergillus.
People who might get this type of infection include those having
chemotherapy, those who have
had a transplant and those whose immune systems are weak.

sus
                                
                                Baca dokumen lengkapnya
                                
                            

Karakteristik produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Caspofungin Accord 50 mg powder for concentrate for solution for
infusion
Caspofungin Accord 70 mg powder for concentrate for solution for
infusion
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
_ _
Caspofungin Accord 50 mg powder for concentrate for solution for
infusion
Each vial contains 50 mg caspofungin (as acetate).
Caspofungin Accord 70 mg powder for concentrate for solution for
infusion
Each vial contains 70 mg caspofungin (as acetate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Powder for concentrate for solution for infusion.
White to off-white, powder.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS

Treatment of invasive candidiasis in adult or paediatric patients.

Treatment of invasive aspergillosis in adult or paediatric patients
who are refractory to or
intolerant of amphotericin B, lipid formulations of amphotericin B
and/or itraconazole.
Refractoriness is defined as progression of infection or failure to
improve after a minimum of
7 days of prior therapeutic doses of effective antifungal therapy.

Empirical therapy for presumed fungal infections (such as Candida or
Aspergillus) in febrile,
neutropaenic adult or paediatric patients.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Caspofungin should be initiated by a physician experienced in the
management of invasive fungal
infections.
Posology
_Adult patients_
A single 70 mg loading dose should be administered on Day-1, followed
by 50 mg daily thereafter. In
patients weighing more than 80 kg, after the initial 70 mg loading
dose, caspofungin 70 mg daily is
recommended (see section 5.2). No dosage adjustment is necessary based
on gender or race (see
section 5.2).
_Paediatric patients (12 months to 17 years) _
In paediatric patients (12 months to 17 years of age), dosing should
be based on the patient’s body
surface area (see Instructions for Use in Paediatric Patients,
Mosteller
1
Formula). For all indications, a
single 70-mg/m
2
lo
                                
                                Baca dokumen lengkapnya
                                
                            

Dokumen dalam bahasa lain

Selebaran informasi Selebaran informasi Bulgar 05-03-2020
Karakteristik produk Karakteristik produk Bulgar 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Bulgar 21-03-2016
Selebaran informasi Selebaran informasi Spanyol 05-03-2020
Karakteristik produk Karakteristik produk Spanyol 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Spanyol 21-03-2016
Selebaran informasi Selebaran informasi Cheska 05-03-2020
Karakteristik produk Karakteristik produk Cheska 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Cheska 21-03-2016
Selebaran informasi Selebaran informasi Dansk 05-03-2020
Karakteristik produk Karakteristik produk Dansk 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Dansk 21-03-2016
Selebaran informasi Selebaran informasi Jerman 05-03-2020
Karakteristik produk Karakteristik produk Jerman 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Jerman 21-03-2016
Selebaran informasi Selebaran informasi Esti 05-03-2020
Karakteristik produk Karakteristik produk Esti 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Esti 21-03-2016
Selebaran informasi Selebaran informasi Yunani 05-03-2020
Karakteristik produk Karakteristik produk Yunani 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Yunani 21-03-2016
Selebaran informasi Selebaran informasi Prancis 05-03-2020
Karakteristik produk Karakteristik produk Prancis 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Prancis 21-03-2016
Selebaran informasi Selebaran informasi Italia 05-03-2020
Karakteristik produk Karakteristik produk Italia 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Italia 21-03-2016
Selebaran informasi Selebaran informasi Latvi 05-03-2020
Karakteristik produk Karakteristik produk Latvi 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Latvi 21-03-2016
Selebaran informasi Selebaran informasi Lituavi 05-03-2020
Karakteristik produk Karakteristik produk Lituavi 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Lituavi 21-03-2016
Selebaran informasi Selebaran informasi Hungaria 05-03-2020
Karakteristik produk Karakteristik produk Hungaria 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Hungaria 21-03-2016
Selebaran informasi Selebaran informasi Malta 05-03-2020
Karakteristik produk Karakteristik produk Malta 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Malta 21-03-2016
Selebaran informasi Selebaran informasi Belanda 05-03-2020
Karakteristik produk Karakteristik produk Belanda 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Belanda 21-03-2016
Selebaran informasi Selebaran informasi Polski 05-03-2020
Karakteristik produk Karakteristik produk Polski 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Polski 21-03-2016
Selebaran informasi Selebaran informasi Portugis 05-03-2020
Karakteristik produk Karakteristik produk Portugis 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Portugis 21-03-2016
Selebaran informasi Selebaran informasi Rumania 05-03-2020
Karakteristik produk Karakteristik produk Rumania 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Rumania 21-03-2016
Selebaran informasi Selebaran informasi Slovak 05-03-2020
Karakteristik produk Karakteristik produk Slovak 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Slovak 21-03-2016
Selebaran informasi Selebaran informasi Sloven 05-03-2020
Karakteristik produk Karakteristik produk Sloven 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Sloven 21-03-2016
Selebaran informasi Selebaran informasi Suomi 05-03-2020
Karakteristik produk Karakteristik produk Suomi 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Suomi 21-03-2016
Selebaran informasi Selebaran informasi Swedia 05-03-2020
Karakteristik produk Karakteristik produk Swedia 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Swedia 21-03-2016
Selebaran informasi Selebaran informasi Norwegia 05-03-2020
Karakteristik produk Karakteristik produk Norwegia 05-03-2020
Selebaran informasi Selebaran informasi Islandia 05-03-2020
Karakteristik produk Karakteristik produk Islandia 05-03-2020
Selebaran informasi Selebaran informasi Kroasia 05-03-2020
Karakteristik produk Karakteristik produk Kroasia 05-03-2020
Laporan Penilaian publik Laporan Penilaian publik Kroasia 21-03-2016

Peringatan pencarian terkait dengan produk ini