Belgia - engelsk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

roche sa-nv - interferon alfa-2a 18000000 iu/ml - solution for injection in pre-filled syringe - 9 miu - interferon alfa-2a 9000000 iu - interferon alfa-2a

Singapore - engelsk - HSA (Health Sciences Authority)

msd pharma (singapore) pte. ltd. - interferon alfa-2b - injection - 30 miu/pen

Tyrkia - tyrkisk - TİTCK (Türkİye İlaç Ve Tibbİ Cİhaz Kurumu)

merck sharp dohme İlaÇlari ltd. Ştİ. - interferon alfa-2b - interferon alfa-2b

Tyskland - tysk - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

basotherm gmbh & co.kg - interferon alfa-2c - lösung - interferon alfa-2c 4.7µg

USA - engelsk - NLM (National Library of Medicine)

merck sharp & dohme llc - interferon alfa-2b (unii: 43k1w2t1m6) (interferon alfa-2b - unii:43k1w2t1m6) - interferon alfa-2b 38 ug in 1 ml - intron® a is indicated for the treatment of patients 18 years of age or older with hairy cell leukemia. intron a is indicated as adjuvant to surgical treatment in patients 18 years of age or older with malignant melanoma who are free of disease but at high risk for systemic recurrence, within 56 days of surgery. intron a is indicated for the initial treatment of clinically aggressive (see clinical pharmacology ) follicular non-hodgkin's lymphoma in conjunction with anthracycline-containing combination chemotherapy in patients 18 years of age or older. efficacy of intron a therapy in patients with low-grade, low-tumor burden follicular non-hodgkin's lymphoma has not been demonstrated. intron a is indicated for intralesional treatment of selected patients 18 years of age or older with condylomata acuminata involving external surfaces of the genital and perianal areas (see dosage and administration ). the use of this product in adolescents has not been studied. intron a is indicated for the treatment of select

Den europeiske union - maltesisk - EMA (European Medicines Agency)

merck sharp & dohme b.v. - peginterferon alfa-2b - epatite Ċ, kronika - immunostimulanti, - adults (tritherapy)pegintron in combination with ribavirin and boceprevir (tritherapy) is indicated for the treatment of chronic-hepatitis-c (chc) genotype-1 infection in adult patients (18 years of age and older) with compensated liver disease who are previously untreated or who have failed previous therapy. jekk jogħġbok irreferi għall-ribavirin u boceprevir-sommarji tal-karatteristiċi tal-prodott (smpcs) meta pegintron ikun ser jintuża flimkien ma ' dawn il-mediċini. adults (bitherapy and monotherapy)pegintron is indicated for the treatment of adult patients (18 years of age and older) with chc who are positive for hepatitis-c-virus rna (hcv-rna), including patients with compensated cirrhosis and / or co-infected with clinically stable hiv. pegintron f'kombinazzjoni ma 'ribavirin (bitherapy) huwa indikat għall-kura ta chc infezzjoni fil-pazjenti adulti li ma kienux trattati qabel inkluż pazjenti b'hiv klinikament stabbli ko-infezzjoni u f'pazjenti adulti li jkunu fallew it-trattament preċedenti bl-interferon-alpha (pegilata jew mhux pegilata) u terapija kombinata b'ribavirin jew ma' interferon-alpha monoterapija. il-monoterapija b'interferon, li tinkludi pegintron, tintuża l-aktar f'każ ta 'intolleranza jew ta' kontra-indikazzjoni għal ribavirin. jekk jogħġbok irreferi għall-ribavirin smpc meta pegintron ikun ser jintuża flimkien ma ' ribavirin. paediatric population (bitherapy)pegintron is indicated in a combination regimen with ribavirin for the treatment of children three years of age and older and adolescents who have chc, previously untreated, without liver decompensation, and who are positive for hcv-rna. meta tiddeċiedi li ma li tipposponi it-trattament sakemm il-ħajja adulta, huwa importanti li wieħed jikkunsidra li l-terapija kombinata indotta-inibizzjoni tat-tkabbir li jista'jkun irriversibbli f'xi pazjenti. id-deċiżjoni li l-kura għandha tittieħed każ b'każ. jekk jogħġbok irreferi għall-ribavirin smpc għal kapsuli jew soluzzjoni orali meta pegintron ikun ser jintuża flimkien ma ' ribavirin.

Den europeiske union - maltesisk - EMA (European Medicines Agency)

merck sharp dohme ltd  - peginterferon alfa-2b - epatite Ċ, kronika - immunostimulanti, - adults (tritherapy)viraferonpeg in combination with ribavirin and boceprevir (tritherapy) is indicated for the treatment of chronic-hepatitis-c (chc) genotype-1 infection in adult patients (18 years of age and older) with compensated liver disease who are previously untreated or who have failed previous therapy. jekk jogħġbok irreferi għall-ribavirin u boceprevir-sommarji tal-karatteristiċi tal-prodott (smpcs) meta viraferonpeg ikun ser jintuża flimkien ma ' dawn il-mediċini. adults (bitherapy and monotherapy)viraferonpeg is indicated for the treatment of adult patients (18 years of age and older) with chc who are positive for hepatitis-c-virus rna (hcv-rna), including patients with compensated cirrhosis and / or co-infected with clinically stable hiv. viraferonpeg f'kombinazzjoni ma ' ribavirin (bitherapy) huwa indikat għall-kura ta chc infezzjoni fil-pazjenti adulti li ma kienux trattati qabel inkluż pazjenti b'hiv klinikament stabbli ko-infezzjoni u f'pazjenti adulti li jkunu fallew it-trattament preċedenti bl-interferon-alpha (pegilata jew mhux pegilata) u terapija kombinata b'ribavirin jew monoterapija b'interferon alfa. il-monoterapija b'interferon, li tinkludi viraferonpeg, tintuża l-aktar f'każ ta 'intolleranza jew ta' kontra-indikazzjoni għal ribavirin. jekk jogħġbok irreferi għall-ribavirin smpc meta viraferonpeg ikun ser jintuża flimkien ma ' ribavirin. paediatric population (bitherapy)viraferonpeg is indicated in a combination regimen with ribavirin for the treatment of children three years of age and older and adolescents, who have chronic hepatitis c, previously untreated, without liver decompensation, and who are positive for hcv-rna. meta tiddeċiedi li ma li tipposponi it-trattament sakemm il-ħajja adulta, huwa importanti li wieħed jikkunsidra li l-terapija kombinata indotta-inibizzjoni tat-tkabbir li jista'jkun irriversibbli f'xi pazjenti. id-deċiżjoni li l-kura għandha tittieħed każ b'każ. jekk jogħġbok irreferi għall-ribavirin smpc għal kapsuli jew soluzzjoni orali meta viraferonpeg ikun ser jintuża flimkien ma ' ribavirin.

Den europeiske union - engelsk - EMA (European Medicines Agency)

merck sharp & dohme b.v. - peginterferon alfa-2b - hepatitis c, chronic - immunostimulants, - adults (tritherapy)pegintron in combination with ribavirin and boceprevir (tritherapy) is indicated for the treatment of chronic-hepatitis-c (chc) genotype-1 infection in adult patients (18 years of age and older) with compensated liver disease who are previously untreated or who have failed previous therapy.please refer to the ribavirin and boceprevir summaries of product characteristics (smpcs) when pegintron is to be used in combination with these medicines.adults (bitherapy and monotherapy)pegintron is indicated for the treatment of adult patients (18 years of age and older) with chc who are positive for hepatitis-c-virus rna (hcv-rna), including patients with compensated cirrhosis and / or co-infected with clinically stable hiv.pegintron in combination with ribavirin (bitherapy) is indicated for the treatment of chc infection in adult patients who are previously untreated including patients with clinically stable hiv co-infection and in adult patients who have failed previous treatment with interferon-alpha (pegylated or non-pegylated) and ribavirin combination therapy or interferon-alpha monotherapy.interferon monotherapy, including pegintron, is indicated mainly in case of intolerance or contraindication to ribavirin.please refer to the ribavirin smpc when pegintron is to be used in combination with ribavirin.paediatric population (bitherapy)pegintron is indicated in a combination regimen with ribavirin for the treatment of children three years of age and older and adolescents who have chc, previously untreated, without liver decompensation, and who are positive for hcv-rna.when deciding not to defer treatment until adulthood, it is important to consider that the combination therapy induced a growth inhibition that may be irreversible in some patients. the decision to treat should be made on a case-by-case basis.please refer to the ribavirin smpc for capsules or oral solution when pegintron is to be used in combination with ribavirin.

Israel - engelsk - Ministry of Health

merck serono ltd - interferon beta 1a - solution for injection - interferon beta 1a 44 mcg/ml - interferon beta-1a - interferon beta-1a - rebif (interferone beta-1a) is indicated for the treatment of patients with relapsing forms of multiple sclerosis to decrease the frequency of clinical exacerbations and delay the accumulation of physical disability. efficacy of rebif in chronic progressive multiple sclerosis has not been established.

Australia - engelsk - Department of Health (Therapeutic Goods Administration)

merck sharp & dohme (australia) pty ltd - interferon alfa-2b -