Posaconazole AHCL

Country: Kesatuan Eropah

Bahasa: Inggeris

Sumber: EMA (European Medicines Agency)

Beli sekarang

Download Risalah maklumat (PIL)
22-04-2024
Download Ciri produk (SPC)
22-04-2024
Download Laporan Penilaian Awam (PAR)
21-09-2023

Bahan aktif:

posaconazole

Boleh didapati daripada:

Accord Healthcare S.L.U.

Kod ATC:

J02AC04

INN (Nama Antarabangsa):

posaconazole

Kumpulan terapeutik:

Antimycotics for systemic use

Kawasan terapeutik:

Mycoses

Tanda-tanda terapeutik:

Posaconazole AHCL oral suspension is indicated for use in the treatment of the following fungal infections in adults:Invasive aspergillosis in patients with disease that is refractory to amphotericin B or itraconazole or in patients who are intolerant of these medicinal products;Fusariosis in patients with disease that is refractory to amphotericin B or in patients who are intolerant of amphotericin B;Chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;Coccidioidomycosis in patients with disease that is refractory to amphotericin B, itraconazole or fluconazole or in patients who are intolerant of these medicinal products.Oropharyngeal candidiasis: as first-line therapy in patients who have severe disease or are immunocompromised, in whom response to topical therapy is expected to be poor.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.Posaconazole AHCL oral suspension is also indicated for prophylaxis of invasive fungal infections in the following patients:Patients receiving remission-induction chemotherapy for acute myelogenous leukemia (AML) or myelodysplastic syndromes (MDS) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;Hematopoietic stem cell transplant (HSCT) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections.

Ringkasan produk:

Revision: 6

Status kebenaran:

Authorised

Tarikh kebenaran:

2019-07-25

Risalah maklumat

                                29
B. PACKAGE LEAFLET
30
PACKAGE LEAFLET: INFORMATION FOR THE USER
POSACONAZOLE AHCL 40 MG/ML ORAL SUSPENSION
posaconazole
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING 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, pharmacist, 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, pharmacist or nurse.
This includes any possible
side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Posaconazole AHCL is and what it is used for
2.
What you need to know before you take Posaconazole AHCL
3.
How to take Posaconazole AHCL
4.
Possible side effects
5.
How to store Posaconazole AHCL
6.
Contents of the pack and other information
1.
WHAT POSACONAZOLE AHCL IS AND WHAT IT IS USED FOR
Posaconazole AHCL contains a medicine called posaconazole. This
belongs to a group of medicines
called “antifungals”. It is used to prevent and treat many
different fungal infections.
This medicine works by killing or stopping the growth of some types of
fungi that can cause
infections.
Posaconazole AHCL can be used in adults to treat the following types
of fungal infections when other
antifungal medicines have not worked or you have had to stop taking
them:
-
infections caused by fungi of the Aspergillus family that have not
improved during treatment
with the anti-fungal medicines amphotericin B or itraconazole or when
these medicines have
had to be stopped;
-
infections caused by fungi of the Fusarium family that have not
improved during treatment with
amphotericin B or when amphotericin B has had to be stopped;
-
infections caused by fungi that cause the conditions known as
“chromoblastomycosis” and
“mycetoma” that have not improved during treatment with
itraconazole or when itraconazole
has had to be
                                
                                Baca dokumen lengkap
                                
                            

Ciri produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Posaconazole AHCL 40 mg/mL oral suspension
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each mL of oral suspension contains 40 mg of posaconazole.
Excipient(s) with known effect
This medicinal product contains approximately 1.75 g of glucose per 5
mL of suspension.
This medicinal product contains up to 5.2 mg propylene glycol (E1520)
per 5ml of suspension.
This medicinal product contains 11.4 mg sodium benzoate (E211) in each
5ml of suspension.
This medicinal product contains up to 0.114 mg benzoic acid (E210) in
each 5ml of suspension.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Oral suspension
White to off-white free flowing suspension.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Posaconazole AHCL oral suspension is indicated for use in the
treatment of the following fungal
infections in adults (see section 5.1):
-
Invasive aspergillosis in patients with disease that is refractory to
amphotericin B or
itraconazole or in patients who are intolerant of these medicinal
products;
-
Fusariosis in patients with disease that is refractory to amphotericin
B or in patients who are
intolerant of amphotericin B;
-
Chromoblastomycosis and mycetoma in patients with disease that is
refractory to itraconazole
or in patients who are intolerant of itraconazole;
-
Coccidioidomycosis in patients with disease that is refractory to
amphotericin B, itraconazole or
fluconazole or in patients who are intolerant of these medicinal
products.
-
Oropharyngeal candidiasis: as first-line therapy in patients who have
severe disease or are
immunocompromised, in whom response to topical therapy is expected to
be poor.
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.
Posaconazole AHCL oral suspension is also indicated for prophylaxis of
invasive fungal infections in
the following patients:
-
Patients receiving remission
                                
                                Baca dokumen lengkap
                                
                            

Dokumen dalam bahasa lain

Risalah maklumat Risalah maklumat Bulgaria 22-04-2024
Ciri produk Ciri produk Bulgaria 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Bulgaria 21-09-2023
Risalah maklumat Risalah maklumat Sepanyol 22-04-2024
Ciri produk Ciri produk Sepanyol 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Sepanyol 21-09-2023
Risalah maklumat Risalah maklumat Czech 22-04-2024
Ciri produk Ciri produk Czech 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Czech 21-09-2023
Risalah maklumat Risalah maklumat Denmark 22-04-2024
Ciri produk Ciri produk Denmark 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Denmark 21-09-2023
Risalah maklumat Risalah maklumat Jerman 22-04-2024
Ciri produk Ciri produk Jerman 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Jerman 21-09-2023
Risalah maklumat Risalah maklumat Estonia 22-04-2024
Ciri produk Ciri produk Estonia 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Estonia 21-09-2023
Risalah maklumat Risalah maklumat Greek 22-04-2024
Ciri produk Ciri produk Greek 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Greek 21-09-2023
Risalah maklumat Risalah maklumat Perancis 22-04-2024
Ciri produk Ciri produk Perancis 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Perancis 21-09-2023
Risalah maklumat Risalah maklumat Itali 22-04-2024
Ciri produk Ciri produk Itali 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Itali 21-09-2023
Risalah maklumat Risalah maklumat Latvia 22-04-2024
Ciri produk Ciri produk Latvia 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Latvia 21-09-2023
Risalah maklumat Risalah maklumat Lithuania 22-04-2024
Ciri produk Ciri produk Lithuania 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Lithuania 21-09-2023
Risalah maklumat Risalah maklumat Hungary 22-04-2024
Ciri produk Ciri produk Hungary 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Hungary 21-09-2023
Risalah maklumat Risalah maklumat Malta 22-04-2024
Ciri produk Ciri produk Malta 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Malta 21-09-2023
Risalah maklumat Risalah maklumat Belanda 22-04-2024
Ciri produk Ciri produk Belanda 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Belanda 21-09-2023
Risalah maklumat Risalah maklumat Poland 22-04-2024
Ciri produk Ciri produk Poland 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Poland 21-09-2023
Risalah maklumat Risalah maklumat Portugis 22-04-2024
Ciri produk Ciri produk Portugis 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Portugis 21-09-2023
Risalah maklumat Risalah maklumat Romania 22-04-2024
Ciri produk Ciri produk Romania 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Romania 21-09-2023
Risalah maklumat Risalah maklumat Slovak 22-04-2024
Ciri produk Ciri produk Slovak 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Slovak 21-09-2023
Risalah maklumat Risalah maklumat Slovenia 22-04-2024
Ciri produk Ciri produk Slovenia 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Slovenia 21-09-2023
Risalah maklumat Risalah maklumat Finland 22-04-2024
Ciri produk Ciri produk Finland 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Finland 21-09-2023
Risalah maklumat Risalah maklumat Sweden 22-04-2024
Ciri produk Ciri produk Sweden 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Sweden 21-09-2023
Risalah maklumat Risalah maklumat Norway 22-04-2024
Ciri produk Ciri produk Norway 22-04-2024
Risalah maklumat Risalah maklumat Iceland 22-04-2024
Ciri produk Ciri produk Iceland 22-04-2024
Risalah maklumat Risalah maklumat Croat 22-04-2024
Ciri produk Ciri produk Croat 22-04-2024
Laporan Penilaian Awam Laporan Penilaian Awam Croat 21-09-2023

Cari amaran yang berkaitan dengan produk ini