Европейский союз - греческий - EMA (European Medicines Agency)

astrazeneca ab - osimertinib mesilate - Καρκίνωμα, μη μικροκυτταρικός πνεύμονας - Άλλοι αντινεοπλασματικοί παράγοντες, αναστολείς πρωτεϊνικής κινάσης - tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations- the first-line treatment of adult patients nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc. tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations. - the first-line treatment of adult patients with locally advanced or metastatic nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc.

Кипр - греческий - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

delorbis pharmaceuticals ltd (0000009620) 17 athinon street, ergates industrial area, lefkosia, 2081, 28629 - meloxicam - tablets - 15mg - meloxicam (0071125387) 15mg - meloxicam

Кипр - греческий - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

delorbis pharmaceuticals ltd (0000009620) 17 athinon street, ergates industrial area, lefkosia, 2081, 28629 - meloxicam - tablets - 7.5mg - meloxicam (0071125387) 7,5mg - meloxicam

Европейский союз - греческий - EMA (European Medicines Agency)

abbvie deutschland gmbh co. kg - venetoclax - Λευχαιμία, λεμφοκυτταρική, χρόνια, Β-κυτταρική - Αντινεοπλασματικοί παράγοντες - venclyxto in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll) (see section 5. venclyxto in combination with rituximab is indicated for the treatment of adult patients with cll who have received at least one prior therapy. venclyxto monotherapy is indicated for the treatment of cll:- in the presence of 17p deletion or tp53 mutation in adult patients who are unsuitable for or have failed a b cell receptor pathway inhibitor, or- in the absence of 17p deletion or tp53 mutation in adult patients who have failed both chemoimmunotherapy and a b-cell receptor pathway inhibitor. venclyxto in combination with a hypomethylating agent is indicated for the treatment of adult patients with newly  diagnosed acute myeloid leukaemia (aml) who are ineligible for intensive chemotherapy.

Кипр - греческий - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

medochemie ltd (0000003169) 1-10 constantinoupoleos str, lemesos, 3011, 51409 (3505) - levofloxacin hemihydrate - film coated tablets - 250mg - levofloxacin hemihydrate (8000003372) 256mg - levofloxacin

Кипр - греческий - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

medochemie ltd (0000003169) 1-10 constantinoupoleos str, lemesos, 3011, 51409 (3505) - levofloxacin hemihydrate - film coated tablets - 500mg - levofloxacin hemihydrate (8000003372) 512mg - levofloxacin

Кипр - греческий - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

medochemie ltd (0000003169) 1-10 constantinoupoleos str, lemesos, 3011, 51409 (3505) - lincomycin hydrochloride monohydrate - solution for injection or infusion - 300mg/ml - lincomycin hydrochloride monohydrate (0007179499) 340,2mg - lincomycin

Кипр - греческий - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

medochemie ltd (0000003169) 1-10 constantinoupoleos str, lemesos, 3011, 51409 (3505) - ciprofloxacin hydrochloride monohydrate - film coated tablets - 250mg - ciprofloxacin hydrochloride monohydrate (8000002035) 291,5mg - ciprofloxacin

Кипр - греческий - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

medochemie ltd (0000003169) 1-10 constantinoupoleos str, lemesos, 3011, 51409 (3505) - ciprofloxacin hydrochloride monohydrate - film coated tablets - 500mg - ciprofloxacin hydrochloride monohydrate (8000002035) 583mg - ciprofloxacin

Европейский союз - греческий - 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.