Noxafil

Država: Europska Unija

Jezik: latvijski

Izvor: EMA (European Medicines Agency)

Uputa o lijeku Uputa o lijeku (PIL)
20-06-2023
Svojstava lijeka Svojstava lijeka (SPC)
20-06-2023

Aktivni sastojci:

posaconazole

Dostupno od:

Merck Sharp and Dohme B.V

ATC koda:

J02AC04

INN (International ime):

posaconazole

Terapijska grupa:

Antimycotics sistēmiskai lietošanai

Područje terapije:

Candidiasis; Mycoses; Coccidioidomycosis; Aspergillosis

Terapijske indikacije:

Noxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 un 5. 1):- Invasive aspergillosisNoxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections  4. 2 un 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. Refractoriness ir definēta kā progresēšanu infekcijas vai nespēja uzlabot pēc vismaz 7 dienas pirms terapijas devas efektīvs pretsēnīšu terapija. Noxafil gastro-resistant tablets are also indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections 4. 2 un 5. 1):- Patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (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. Please refer to the Summary of Product Characteristics of Noxafil oral suspension for use in oropharyngeal candidiasis.  Noxafil concentrate for solution for infusion is indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 un 5. 1):- Invasive aspergillosisNoxafil concentrate for solution for infusion is indicated for use in the treatment of the following fungal infections in adult and paediatric patients from 2 years of age (see sections 4. 2 un 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. Refractoriness ir definēta kā progresēšanu infekcijas vai nespēja uzlabot pēc vismaz 7 dienas pirms terapijas devas efektīvs pretsēnīšu terapija. Noxafil concentrate for solution for infusion is also indicated for prophylaxis of invasive fungal infections in the following adult and paediatric patients from 2 years of age (see sections 4. 2 un 5. 1):- Patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (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 (GVHD) and who are at high risk of developing invasive fungal infections. Please refer to the Summary of Product Characteristics of Noxafil oral suspension for use in oropharyngeal candidiasis.  Noxafil gastro resistant powder and solvent for oral suspension is indicated for use in the treatment of the following fungal infections in paediatric patients from 2 years of age (see sections 4. 2 un 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. Refractoriness ir definēta kā progresēšanu infekcijas vai nespēja uzlabot pēc vismaz 7 dienas pirms terapijas devas efektīvs pretsēnīšu terapija. Noxafil gastro-resistant powder and solvent for oral suspension is indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2  years of age:- Patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (AML) or myelodysplastic syndromes (MDS) expected to result in prolonged neutropenia and who are at high  risk of developing invasive fungal infections;- Haematopoietic 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. Please refer to the Summary of Product Characteristics of Noxafil concentrate for solution for infusion and the gastro-resistant tablets for use in primary treatment of invasive aspergillosis. Please refer to the Summary of Product Characteristics of Noxafil oral suspension for use in oropharyngeal candidiasis.  Noxafil oral suspension is indicated for use in the treatment of the following fungal infections in adults (see section 5. 1):- Invazīvās aspergillosis pacientiem ar slimību, kas ir ugunsizturīgi, lai amfotericīna B vai itraconazole, vai pacientiem, kuri nepanes no šīm zālēm;- Fusariosis pacientiem ar slimību, kas ir ugunsizturīgi, lai amfotericīna B, vai pacientiem, kuri nepanes no amfotericīna B;- Chromoblastomycosis un mycetoma pacientiem ar slimību, kas ir ugunsizturīgi, lai itraconazole, vai pacientiem, kuri nepanes no itraconazole;- Coccidioidomycosis pacientiem ar slimību, kas ir ugunsizturīgi, lai amfotericīna B, itraconazole vai fluconazole, vai pacientiem, kuri nepanes no šīm zālēm;- Orofaringālas kandidoze: kā pirmās līnijas terapija pacientiem, kuriem ir smagas slimības vai pat cilvēkiem ar traucētu imūnsistēmu, kuriem atbildes uz aktuāliem terapija ir sagaidāms, ka būs slikti. Refractoriness ir definēta kā progresēšanu infekcijas vai nespēja uzlabot pēc vismaz 7 dienas pirms terapijas devas efektīvs pretsēnīšu terapija. Noxafil oral suspension is also indicated for prophylaxis of invasive fungal infections in the following patients:- Patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (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. Please refer to the Summary of Product Characteristics of Noxafil concentrate for solution for infusion and the gastro-resistant tablets for use in primary treatment of invasive aspergillosis.

Proizvod sažetak:

Revision: 37

Status autorizacije:

Autorizēts

Datum autorizacije:

2005-10-25

Uputa o lijeku

                                1
I
PIELIKUMS
ZĀĻU APRAKSTS
2
1.
ZĀĻU NOSAUKUMS
Noxafil 40
mg/ml suspensija iekšķīgai lietošanai
2.
KVALITATĪVAIS UN KVANTITATĪVAIS SASTĀVS
Katrā ml suspensijas iekšķīgai lietošanai ir 40
mg posakonazola (
posaconazolum
).
Palīgvi
elas
ar zināmu iedarbību
5
ml suspensijas satur
1,75 g glikozes.
5
ml suspensijas satur
10 mg
nātrija benzoāta (E211)
.
5
ml suspensijas satur 1,
25 mg
benzilspirta
.
5
ml suspensijas satur
24,75 mg
propilēnglikola
(E1520).
Pilnu palīgvielu sarakstu skatīt
6.1.
apakšpunktā.
3.
ZĀĻU FORMA
Suspensija iekšķīgai lietošanai
Balta suspensija
4.
KLĪNISKĀ INFORMĀCIJA
4.1.
Terapeitiskās indikācijas
Noxafil
suspensija iekšķīgai lietošanai indicēts lietošanai šādu
sēnīšinfekciju ārstēšan
ai
pieaugušajiem
(skatī
t 5.1.
apakšpunkt
u):
-
invazīva aspergiloze pacientiem, kas nepakļaujas ārstēšanai ar
amfotericīnu
B vai itrakonazolu,
vai arī pacientiem, kuri nepanes šīs zāles;
-
fuza
rioze pacientiem, kas nepakļaujas ārstēšanai ar amfotericīnu
B, vai arī pacientiem, k
uri
nepanes amfotericīnu
B;
-
hromoblastomikoze un micetoma pacientiem, kas nepakļaujas
ārstēšanai ar itrakonazolu, vai arī
pacientiem, kuri nepanes itrakonazolu;
-
kokcidioidomikoze pacientiem, kas nepakļaujas ārstēšanai ar
amfotericīnu
B, itrakonazolu va
i
f
lukonazolu, vai arī pacientiem, kuri nepanes šīs zāles;
-
orofaringeālas kandidozes gadījumā: par pirmās kārtas terapiju
slimniekiem, kam ir smaga
slimība vai imūndeficīts, ja paredzams, ka lokālā terapija būs
mazefektīva.
Refraktivitāte tiek definēta
k
ā infekcijas progresēšana vai neveiksmīga ārstēšana pēc vismaz
7
dienu
efektīvas pretsēnīšu terapijas terapeitiskās devās
.
Noxafil
suspensija iekšķīgai lietošanai indicēts arī pret invazīvu
sēnīšinfekciju profilaksei šādiem
pacientiem:
-
pacientiem ar a
k
ūt
u mieloleikozi (AML) vai mielodisplastiskiem sindromiem (MDS), kas
saņem remisiju ierosinošu ķīmijterapiju, kura, domājams,
izraisīs ilgstošu neit
                                
                                Pročitajte cijeli dokument
                                
                            

Svojstava lijeka

                                1
I
PIELIKUMS
ZĀĻU APRAKSTS
2
1.
ZĀĻU NOSAUKUMS
Noxafil 40
mg/ml suspensija iekšķīgai lietošanai
2.
KVALITATĪVAIS UN KVANTITATĪVAIS SASTĀVS
Katrā ml suspensijas iekšķīgai lietošanai ir 40
mg posakonazola (
posaconazolum
).
Palīgvi
elas
ar zināmu iedarbību
5
ml suspensijas satur
1,75 g glikozes.
5
ml suspensijas satur
10 mg
nātrija benzoāta (E211)
.
5
ml suspensijas satur 1,
25 mg
benzilspirta
.
5
ml suspensijas satur
24,75 mg
propilēnglikola
(E1520).
Pilnu palīgvielu sarakstu skatīt
6.1.
apakšpunktā.
3.
ZĀĻU FORMA
Suspensija iekšķīgai lietošanai
Balta suspensija
4.
KLĪNISKĀ INFORMĀCIJA
4.1.
Terapeitiskās indikācijas
Noxafil
suspensija iekšķīgai lietošanai indicēts lietošanai šādu
sēnīšinfekciju ārstēšan
ai
pieaugušajiem
(skatī
t 5.1.
apakšpunkt
u):
-
invazīva aspergiloze pacientiem, kas nepakļaujas ārstēšanai ar
amfotericīnu
B vai itrakonazolu,
vai arī pacientiem, kuri nepanes šīs zāles;
-
fuza
rioze pacientiem, kas nepakļaujas ārstēšanai ar amfotericīnu
B, vai arī pacientiem, k
uri
nepanes amfotericīnu
B;
-
hromoblastomikoze un micetoma pacientiem, kas nepakļaujas
ārstēšanai ar itrakonazolu, vai arī
pacientiem, kuri nepanes itrakonazolu;
-
kokcidioidomikoze pacientiem, kas nepakļaujas ārstēšanai ar
amfotericīnu
B, itrakonazolu va
i
f
lukonazolu, vai arī pacientiem, kuri nepanes šīs zāles;
-
orofaringeālas kandidozes gadījumā: par pirmās kārtas terapiju
slimniekiem, kam ir smaga
slimība vai imūndeficīts, ja paredzams, ka lokālā terapija būs
mazefektīva.
Refraktivitāte tiek definēta
k
ā infekcijas progresēšana vai neveiksmīga ārstēšana pēc vismaz
7
dienu
efektīvas pretsēnīšu terapijas terapeitiskās devās
.
Noxafil
suspensija iekšķīgai lietošanai indicēts arī pret invazīvu
sēnīšinfekciju profilaksei šādiem
pacientiem:
-
pacientiem ar a
k
ūt
u mieloleikozi (AML) vai mielodisplastiskiem sindromiem (MDS), kas
saņem remisiju ierosinošu ķīmijterapiju, kura, domājams,
izraisīs ilgstošu neit
                                
                                Pročitajte cijeli dokument
                                
                            

Dokumenti na drugim jezicima

Uputa o lijeku Uputa o lijeku bugarski 20-06-2023
Svojstava lijeka Svojstava lijeka bugarski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog bugarski 26-01-2022
Uputa o lijeku Uputa o lijeku španjolski 20-06-2023
Svojstava lijeka Svojstava lijeka španjolski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog španjolski 26-01-2022
Uputa o lijeku Uputa o lijeku češki 20-06-2023
Svojstava lijeka Svojstava lijeka češki 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog češki 26-01-2022
Uputa o lijeku Uputa o lijeku danski 20-06-2023
Svojstava lijeka Svojstava lijeka danski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog danski 26-01-2022
Uputa o lijeku Uputa o lijeku njemački 20-06-2023
Svojstava lijeka Svojstava lijeka njemački 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog njemački 26-01-2022
Uputa o lijeku Uputa o lijeku estonski 20-06-2023
Svojstava lijeka Svojstava lijeka estonski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog estonski 26-01-2022
Uputa o lijeku Uputa o lijeku grčki 20-06-2023
Svojstava lijeka Svojstava lijeka grčki 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog grčki 26-01-2022
Uputa o lijeku Uputa o lijeku engleski 20-06-2023
Svojstava lijeka Svojstava lijeka engleski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog engleski 26-01-2022
Uputa o lijeku Uputa o lijeku francuski 20-06-2023
Svojstava lijeka Svojstava lijeka francuski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog francuski 26-01-2022
Uputa o lijeku Uputa o lijeku talijanski 20-06-2023
Svojstava lijeka Svojstava lijeka talijanski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog talijanski 26-01-2022
Uputa o lijeku Uputa o lijeku litavski 20-06-2023
Svojstava lijeka Svojstava lijeka litavski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog litavski 26-01-2022
Uputa o lijeku Uputa o lijeku mađarski 20-06-2023
Svojstava lijeka Svojstava lijeka mađarski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog mađarski 26-01-2022
Uputa o lijeku Uputa o lijeku malteški 20-06-2023
Svojstava lijeka Svojstava lijeka malteški 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog malteški 26-01-2022
Uputa o lijeku Uputa o lijeku nizozemski 20-06-2023
Svojstava lijeka Svojstava lijeka nizozemski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog nizozemski 26-01-2022
Uputa o lijeku Uputa o lijeku poljski 20-06-2023
Svojstava lijeka Svojstava lijeka poljski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog poljski 26-01-2022
Uputa o lijeku Uputa o lijeku portugalski 20-06-2023
Svojstava lijeka Svojstava lijeka portugalski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog portugalski 26-01-2022
Uputa o lijeku Uputa o lijeku rumunjski 20-06-2023
Svojstava lijeka Svojstava lijeka rumunjski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog rumunjski 26-01-2022
Uputa o lijeku Uputa o lijeku slovački 20-06-2023
Svojstava lijeka Svojstava lijeka slovački 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog slovački 26-01-2022
Uputa o lijeku Uputa o lijeku slovenski 20-06-2023
Svojstava lijeka Svojstava lijeka slovenski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog slovenski 26-01-2022
Uputa o lijeku Uputa o lijeku finski 20-06-2023
Svojstava lijeka Svojstava lijeka finski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog finski 26-01-2022
Uputa o lijeku Uputa o lijeku švedski 20-06-2023
Svojstava lijeka Svojstava lijeka švedski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog švedski 26-01-2022
Uputa o lijeku Uputa o lijeku norveški 20-06-2023
Svojstava lijeka Svojstava lijeka norveški 20-06-2023
Uputa o lijeku Uputa o lijeku islandski 20-06-2023
Svojstava lijeka Svojstava lijeka islandski 20-06-2023
Uputa o lijeku Uputa o lijeku hrvatski 20-06-2023
Svojstava lijeka Svojstava lijeka hrvatski 20-06-2023
Izvješće o ocjeni javnog Izvješće o ocjeni javnog hrvatski 26-01-2022

Upozorenja za pretraživanje vezana za ovaj proizvod

Pogledajte povijest dokumenata