Síp - Tiếng Hy Lạp - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

opella healthcare greece single member ltd (opella e.p.e.) (0000011809) syngrou avenue 348 - building a, kallithea, athens, 176 74 - paracetamol; hyoscine butylbromide - film coated tablets - paracetamol (0000103902) 500mg; hyoscine butylbromide (0000149644) 10mg - butylscopolamine and analgesics

Liên Minh Châu Âu - Tiếng Hy Lạp - EMA (European Medicines Agency)

kite pharma eu b.v. - autologous peripheral blood t cells cd4 and cd8 selected and cd3 and cd28 activated transduced with retroviral vector expressing anti-cd19 cd28/cd3-zeta chimeric antigen receptor and cultured (brexucabtagene autoleucel) - Λέμφωμα, mantle-cell - Αντινεοπλασματικοί παράγοντες - mantle cell lymphomatecartus is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl) after two or more lines of systemic therapy including a bruton’s tyrosine kinase (btk) inhibitor. acute lymphoblastic leukaemiatecartus is indicated for the treatment of adult patients 26 years of age and above with relapsed or refractory b-cell precursor acute lymphoblastic leukaemia (all).

Síp - Tiếng Hy Lạp - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

faes farma sa (0000002088) maximo aquirre 14, leioa(vizcaya), 48940 - phenytoin - tablets - 100mg - phenytoin (0000057410) 100mg - phenytoin

Síp - Tiếng Hy Lạp - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

multi-pharm co ltd - ΚΩΔΕΐΝΗ ΦΩΣΦΟΡΙΚΌ ΆΛΑΣ, ΠΑΡΑΚΕΤΑΜΌΛΗ - tablets - 0000052288 - codeine phosphate - 20 mg; 0000103902 - paracetamol - 500 mg - paracetamol, combinations with psycholeptics

Síp - Tiếng Hy Lạp - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

multi-pharm co ltd - ΠΑΡΑΚΕΤΑΜΌΛΗ, ΚΩΔΕΐΝΗ ΦΩΣΦΟΡΙΚΌ ΆΛΑΣ - capsule,hard - 0000103902 - paracetamol - 500 mg; 0000052288 - codeine phosphate - 30 mg - paracetamol, combinations with psycholeptics

Síp - Tiếng Hy Lạp - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

demo s.a. (0000003568) 21st km national road athens-lamia, krioneri, attiki, 14568 - ciprofloxacin lactate - solution for infusion - 2mg/ml - ciprofloxacin lactate (8000002398) 2,54mg - ciprofloxacin

Liên Minh Châu Âu - Tiếng Hy Lạp - EMA (European Medicines Agency)

mylan pharmaceuticals limited - darunavir - hiv Λοιμώξεις - Αντιιικά για συστηματική χρήση - darunavir, co-administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv-1) infection (see section 4. darunavir mylan 75 mg, 150 mg, 300 mg and 600 mg tablets may be used to provide suitable dose regimens (see section 4. 2):Για τη θεραπεία του hiv-1 λοίμωξη σε αντιρετροϊκή θεραπεία (art)-έμπειρους ενήλικες ασθενείς, συμπεριλαμβανομένων και εκείνων που έχουν ιδιαίτερα προ-θεραπεία. Για τη θεραπεία της λοίμωξης από hiv-1 σε παιδιατρικούς ασθενείς από την ηλικία των 3 ετών και τουλάχιστον 15 kg βάρους σώματος. Στην απόφαση να ξεκινήσει θεραπεία με δαρουναβίρη συγχορηγούμενη με μικρή δόση ριτοναβίρης, πρέπει να δίνεται ιδιαίτερη προσοχή στο ιστορικό θεραπείας του κάθε ασθενούς και οι τύποι των μεταλλάξεων που σχετίζονται με διαφορετικούς παράγοντες. genotypic or phenotypic testing (when available) and treatment history should guide the use of darunavir (see sections 4. 2, 4. 4 και 5. Η δαρουναβίρη συγχορηγούμενη με μικρή δόση ριτοναβίρης ενδείκνυται σε συνδυασμό με άλλα αντιρετροϊκά φαρμακευτικά προϊόντα για τη θεραπεία των ασθενών με τον ιό της ανθρώπινης ανοσοανεπάρκειας (hiv-1) .  darunavir co-administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv-1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg) (see section 4.  darunavir mylan 400 mg and 800 mg tablets may be used to provide suitable dose regimens for the treatment of hiv-1 infection in adult and paediatric patients from the age of 3 years and at least 40 kg body weight who are: antiretroviral therapy (art)-naïve (see section 4.  art-experienced with no darunavir resistance associated mutations (drv-rams) and who have plasma hiv-1 rna < 100,000 copies/ml and cd4+ cell count ≥ 100 cells x 10⁶/l. Στην απόφαση να ξεκινήσει θεραπεία με δαρουναβίρη στην προηγούµενη εµπειρία σε ασθενείς, γονοτυπική δοκιμές πρέπει να διέπουν τη χρήση της δαρουναβίρης (βλέπε παραγράφους 4. 2, 4. 3, 4. 4 και 5.

Liên Minh Châu Âu - Tiếng Hy Lạp - EMA (European Medicines Agency)

viiv healthcare bv - dolutegravir - hiv Λοιμώξεις - Αντιιικά για συστηματική χρήση - tivicay is indicated in combination with other anti-retroviral medicinal products for the treatment of human immunodeficiency virus (hiv) infected adults, adolescents and children of at least 6 years of age or older and weighing at least 14 kg. tivicay is indicated in combination with other anti-retroviral medicinal products for the treatment of human immunodeficiency virus (hiv) infected adults, adolescents and children of at least 4 weeks of age or older and weighing at least 3 kg.

Liên Minh Châu Âu - Tiếng Hy Lạp - EMA (European Medicines Agency)

janssen-cilag international nv - darunavir - hiv Λοιμώξεις - Αντιιικά για συστηματική χρήση - prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adult and paediatric patients from the age of 3 years and at least 15 kg body weight. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). in deciding to initiate treatment with prezista co administered with cobicistat or low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista 75 mg, 150 mg, and 600 mg tablets may be used to provide suitable dose regimens:for the treatment of hiv 1 infection in antiretroviral treatment (art) experienced adult patients, including those that have been highly pre treated. for the treatment of hiv 1 infection in paediatric patients from the age of 3 years and at least 15 kg body weight. in deciding to initiate treatment with prezista co administered with low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). prezista 400 mg and 800 mg tablets may be used to provide suitable dose regimens for the treatment of hiv 1 infection in adult and paediatric patients from the age of 3 years and at least 40 kg body weight who are:antiretroviral therapy (art) naïve. art experienced with no darunavir resistance associated mutations (drv rams) and who have plasma hiv 1 rna < 100,000 copies/ml and cd4+ cell count ≥ 100 cells x 106/l. in deciding to initiate treatment with prezista in such art experienced patients, genotypic testing should guide the use of prezista.

Hy Lạp - Tiếng Hy Lạp - Εθνικός Οργανισμός Φαρμάκων

boehringer ingelheim ΕΛΛΑΣ ΑΕ - butylscopolamine and analgesics - ΥΠΟΘΕΤΟ - (10+800)mg/sup - ΦΑΡΜΑΚΕΥΤΙΚΟ ΠΡΟΪΟΝ