Depakine Retard 300 mg Depottablett Σουηδία - Σουηδικά - Läkemedelsverket (Medical Products Agency)

depakine retard 300 mg depottablett

ebb medical ab - natriumvalproat; valproinsyra - depottablett - 300 mg - natriumvalproat 199,8 mg aktiv substans; valproinsyra 87 mg aktiv substans

Depakine Retard 500 mg Depottablett Σουηδία - Σουηδικά - Läkemedelsverket (Medical Products Agency)

depakine retard 500 mg depottablett

ebb medical ab - natriumvalproat; valproinsyra - depottablett - 500 mg - valproinsyra 145 mg aktiv substans; natriumvalproat 333 mg aktiv substans

Depakine Retard 300 mg Depottablett Σουηδία - Σουηδικά - Läkemedelsverket (Medical Products Agency)

depakine retard 300 mg depottablett

ebb medical ab - natriumvalproat; valproinsyra - depottablett - 300 mg - valproinsyra 87 mg aktiv substans; natriumvalproat 199,8 mg aktiv substans

Selexid 200 mg Filmdragerad tablett Σουηδία - Σουηδικά - Läkemedelsverket (Medical Products Agency)

selexid 200 mg filmdragerad tablett

karo pharma ab - pivmecillinamhydroklorid - filmdragerad tablett - 200 mg - pivmecillinamhydroklorid 200 mg aktiv substans - pivmecillinam

Selexid 200 mg Tablett Σουηδία - Σουηδικά - Läkemedelsverket (Medical Products Agency)

selexid 200 mg tablett

orifarm ab - pivmecillinamhydroklorid - tablett - 200 mg - pivmecillinamhydroklorid 200 mg aktiv substans - pivmecillinam

Selexid 200 mg Tablett Σουηδία - Σουηδικά - Läkemedelsverket (Medical Products Agency)

selexid 200 mg tablett

orifarm ab - pivmecillinamhydroklorid - tablett - 200 mg - pivmecillinamhydroklorid 200 mg aktiv substans - pivmecillinam

Selexid 400 mg Filmdragerad tablett Σουηδία - Σουηδικά - Läkemedelsverket (Medical Products Agency)

selexid 400 mg filmdragerad tablett

karo pharma ab - pivmecillinamhydroklorid - filmdragerad tablett - 400 mg - pivmecillinamhydroklorid 400 mg aktiv substans - pivmecillinam

Ceplene Ευρωπαϊκή Ένωση - Σουηδικά - EMA (European Medicines Agency)

ceplene

laboratoires delbert - histamin dihydrochloride - leukemi, myeloid, akut - immunstimulatorer, - ceplene maintenance therapy is indicated for adult patients with acute myeloid leukaemia in first remission concomitantly treated with interleukin-2 (il-2). effekten av ceplene har inte visats fullständigt hos patienter som är äldre än 60 år.

Noxafil Ευρωπαϊκή Ένωση - Σουηδικά - EMA (European Medicines Agency)

noxafil

merck sharp and dohme b.v - posakonazol - candidiasis; mycoses; coccidioidomycosis; aspergillosis - antimykotika för systemisk användning - noxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 och 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 och 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. refraktäritet definieras som utveckling av infektion eller utebliven förbättring efter en vistelse på minst 7 dagar före terapeutiska doser av effektiv antimykotisk terapi. 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 och 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 och 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 och 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. refraktäritet definieras som utveckling av infektion eller utebliven förbättring efter en vistelse på minst 7 dagar före terapeutiska doser av effektiv antimykotisk terapi. 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 och 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 och 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. refraktäritet definieras som utveckling av infektion eller utebliven förbättring efter en vistelse på minst 7 dagar före terapeutiska doser av effektiv antimykotisk terapi. 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):- invasiv aspergillos hos patienter med sjukdom som är refraktära mot amfotericin b eller itrakonazol eller till patienter som är intoleranta mot dessa läkemedel, - fusariosis på patienter med den sjukdom som är refraktära mot amfotericin b eller till patienter som är intoleranta mot amfotericin b;- chromoblastomycosis och mycetoma på patienter med den sjukdom som är refraktära mot itrakonazol eller till patienter som är intoleranta mot itrakonazol;- coccidiomykos på patienter med den sjukdom som är refraktära mot amfotericin b, itrakonazol eller flukonazol eller till patienter som är intoleranta mot dessa läkemedel.- munhåla candidiasis: som första linjens behandling av patienter som har svår sjukdom eller nedsatt immunförsvar, i vilken respons till aktuell terapi väntas dålig. refraktäritet definieras som utveckling av infektion eller utebliven förbättring efter en vistelse på minst 7 dagar före terapeutiska doser av effektiv antimykotisk terapi. 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.

Vfend Ευρωπαϊκή Ένωση - Σουηδικά - EMA (European Medicines Agency)

vfend

pfizer europe ma eeig - vorikonazol - candidiasis; mycoses; aspergillosis - antimykotika för systemisk användning - vorikonazol är ett brett spektrum, triazol svampdödande agent och är indicerat för vuxna och barn i åldern 2 år och uppåt enligt följande: - behandling av invasiv aspergillos, behandling av i candidaemianon-neutropena patienter, behandling av flukonazol-resistenta allvarliga invasiva candida-infektioner (inklusive c. krusei);behandling av allvarliga svampinfektioner orsakade av scedosporium spp. och fusarium spp.. vfend bör ges främst till patienter med progressiva, möjligen livshotande infektioner. profylax av invasiva svampinfektioner i hög risk allogen hematopoetisk stamcellstransplantation (hsct) mottagare.