Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

bayer animal health gmbh (0000007180) d-51368 leverkusen, germany, leverkusen, d-51368 - propoxur; propoxur - medicated collar - small: 1,234 g, large: 4,442 g - propoxur (0000114261) 1.234g; propoxur (0000114261) 4.442g - propoxur

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

lavipharm hellas ae - roxatidine - ΔΙΣΚΙΟ ΕΛΕΓΧΟΜΕΝΗΣ ΑΠΟΔΕΣΜΕΥΣΗΣ ΕΠΙΚΑΛΥΜΜΕΝΟ ΜΕ ΛΕΠΤΟ ΥΜΕΝΙΟ - 75mg/tab - ΦΑΡΜΑΚΕΥΤΙΚΟ ΠΡΟΪΟΝ

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

lavipharm hellas ae - roxatidine - ΔΙΣΚΙΟ ΕΛΕΓΧΟΜΕΝΗΣ ΑΠΟΔΕΣΜΕΥΣΗΣ ΕΠΙΚΑΛΥΜΜΕΝΟ ΜΕ ΛΕΠΤΟ ΥΜΕΝΙΟ - 150mg/tab - ΦΑΡΜΑΚΕΥΤΙΚΟ ΠΡΟΪΟΝ

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

roche registration gmbh - ατεζολιζουμάμπη - carcinoma, transitional cell; carcinoma, non-small-cell lung; urologic neoplasms; breast neoplasms; small cell lung carcinoma - Αντινεοπλασματικοί παράγοντες - urothelial carcinomatecentriq as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc):- after prior platinum containing chemotherapy, or - who are considered cisplatin ineligible, and whose tumours have a pd-l1 expression ≥ 5% (see section 5. non-small cell lung cancer tecentriq, in combination with bevacizumab, paclitaxel and carboplatin, is indicated for the first-line treatment of adult patients with metastatic non-squamous non small cell lung cancer (nsclc). in patients with egfr mutant or alk-positive nsclc, tecentriq, in combination with bevacizumab, paclitaxel and carboplatin, is indicated only after failure of appropriate targeted therapies (see section 5. tecentriq, in combination with nab paclitaxel and carboplatin, is indicated for the first line treatment of adult patients with metastatic non-squamous nsclc who do not have egfr mutant or alk positive nsclc (see section 5. tecentriq as monotherapy is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumours have a pd-l1 expression ≥ 50% tumour cells (tc) or ≥ 10% tumour-infiltrating immune cells (ic) and who do not have egfr mutant or alk-positive nsclc (see section 5. tecentriq ως μονοθεραπεία ενδείκνυται για τη θεραπεία ενηλίκων ασθενών με τοπικά προχωρημένο ή μεταστατικό μη μικροκυτταρικό καρκίνο του πνεύμονα, μετά από προηγούμενη χημειοθεραπεία. patients with egfr mutant or alk positive nsclc should also have received targeted therapies before receiving tecentriq (see section 5. small cell lung cancertecentriq, in combination with carboplatin and etoposide, is indicated for the first-line treatment of adult patients with extensive-stage small cell lung cancer (es-sclc) (see section 5. hepatocellular carcinomatecentriq, in combination with bevacizumab, is indicated for the treatment of adult patients with advanced or unresectable hepatocellular carcinoma (hcc) who have not received prior systemic therapy (see section 5. urothelial carcinomatecentriq as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc):- after prior platinum containing chemotherapy, or- who are considered cisplatin ineligible, and whose tumours have a pd-l1 expression ≥ 5% (see section 5. non-small cell lung cancertecentriq as monotherapy is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumours have a pd-l1 expression ≥ 50% tumour cells (tc) or ≥ 10% tumour-infiltrating immune cells (ic) and who do not have egfr mutant or alk-positive nsclc (see section 5. tecentriq ως μονοθεραπεία ενδείκνυται για τη θεραπεία ενηλίκων ασθενών με τοπικά προχωρημένο ή μεταστατικό μη μικροκυτταρικό καρκίνο του πνεύμονα, μετά από προηγούμενη χημειοθεραπεία. patients with egfr mutant or alk positive nsclc should also have received targeted therapies before receiving tecentriq (see section 5. triple-negative breast cancertecentriq in combination with nab-paclitaxel is indicated for the treatment of adult patients with unresectable locally advanced or metastatic triple-negative breast cancer (tnbc) whose tumours have pd-l1 expression ≥ 1% and who have not received prior chemotherapy for metastatic disease.

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

roche registration gmbh  - entrectinib - cancer; carcinoma, non-small-cell lung - Αντινεοπλασματικοί παράγοντες - rozlytrek as monotherapy is indicated for the treatment of adult and paediatric patients 12 years of age and older with solid tumours expressing a neurotrophic tyrosine receptor kinase (ntrk) gene fusion,who have a disease that is locally advanced, metastatic or where surgical resection is likely to result in severe morbidity, andwho have not received a prior ntrk inhibitorwho have no satisfactory treatment options. rozlytrek as monotherapy is indicated for the treatment of adult patients with ros1 positive, advanced non small cell lung cancer (nsclc) not previously treated with ros1 inhibitors.

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

ΙΦΕΤ ΑΕ 18ο χλμ. Λεωφ. Μαραθώνος,, 153 51 153 51, Παλλήνη Αττικής 210.6603400-6603522 - sol.iv.inf (ΔΙΑΛΥΜΑ ΓΙΑ ΕΝΔΟΦΛΕΒΙΑ ΕΓΧΥΣΗ) - 60mg/3ml

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

ΚΟΛΟΥΤΣΟΥ ΚΩΝ. (0000003755) Π.Κουντουριώτου 6,,144 51,Μεταμόρφωση,gr - Η ΦΛΟΥΜΕΚΊΝΗ - ΚΟΝΙΣ ΓΙΑ ΠΟΣΙΜΟ ΔΙΑΛΥΜΑ - 50% - flumequine 500,00 pd.ora.sol 50% - flumequine - Ορνιθοειδή; Χοίροι - Χρόνοι αναμονής: Ορνιθοειδή 10; Χοίροι 10

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

alapis abee Αυτοκράτορος Νικολάου 2,, 176 71 176 71, Αθήνα 2130175013 (049) - cromoglicate sodium - m.d.nas.sp (ΕΚΝΕΦΩΜΑ ΡΙΝΙΚΟ ΣΤΑΘΕΡΩΝ ΔΟΣΕΩΝ) - 2% (2,6 mg/dose) - cromoglicate sodium 20mg - cromoglicic acid

Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

procter & gamble health germany gmbh (0000011290) sulzbacher strasse 40, schwalbach am taunus, 65824 - pyridoxine hydrochloride; cyanocobalamin; thiamine hydrochloride - solution for injection - pyridoxine hydrochloride (0000058560) 100mg; cyanocobalamin (0000068199) 1mg; thiamine hydrochloride (0000067038) 100mg - vit b1 in comb with vitamin b6 and/or vitamin b12

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

daiichi sankyo europe gmbh - trastuzumab deruxtecan - Νεοπλάσματα του μαστού - Αντινεοπλασματικοί παράγοντες - breast cancerher2-positive breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-positive breast cancer who have received one or more prior anti-her2-based regimens. her2-low breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy (see section 4. non-small cell lung cancer (nsclc)enhertu as monotherapy is indicated for the treatment of adult patients with advanced nsclc whose tumours have an activating her2 (erbb2) mutation and who require systemic therapy following platinum-based chemotherapy with or without immunotherapy. gastric cancerenhertu as monotherapy is indicated for the treatment of adult patients with advanced her2-positive gastric or gastroesophageal junction (gej) adenocarcinoma who have received a prior trastuzumab-based regimen.