ASACOL 400MG GASTRO RESISTANT TABLET Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

asacol 400mg gastro resistant tablet

tillotts pharma gmbh (0000010051) warmbacher str. 80, rheinfelden, 79618 - mesalazine - gastro resistant tablet - 400mg - mesalazine (0000089576) 400mg - mesalazine

ASACOL 4G/100ML ENEMA Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

asacol 4g/100ml enema

tillotts pharma gmbh (0000010051) warmbacher str. 80, rheinfelden, 79618 - mesalazine - enema - 4g/100ml - mesalazine (0000089576) 4g - mesalazine

NEUROBION SOLUTION FOR INJECTION Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

neurobion solution for injection

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

ORAMORPH 10MG/5ML ORAL SOLUTION Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

oramorph 10mg/5ml oral solution

glenwood gmbh (0000011526) arabellastrasse 17, bogenhausen, munich, 81925 - morphine sulfate - oral solution - 10mg/5ml - morphine sulfate (0000064313) 10mg

INSTILLAGEL Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

instillagel

farco-pharma gmbh (0000003089) gereonsmuhlengasse 1-11, cologne, 50670 - propyl parahydroxybenzoate; methyl parahydroxybenzoate; chlorhexidine digluconate; lidocaine hydrochloride - gel - propyl parahydroxybenzoate (0000094133) 0,025%; methyl parahydroxybenzoate (0000099763) 0,06%; chlorhexidine digluconate (8000002620) 0,05%; lidocaine hydrochloride (0000073789) 2% - lidocaine, combinations

NIZORAL 2% CREAM Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

nizoral 2% cream

stada arzneimittel ag (0000009323) stadastrasse 2-18, bad vilbel, d-61118 - ketoconazole - cream - 2% - ketoconazole (0065277421) 20mg - ketoconazole

Tecentriq Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

tecentriq

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.

Enhertu Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

enhertu

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.

Skyrizi Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

skyrizi

abbvie deutschland gmbh & co. kg - risankizumab - psoriasis; arthritis, psoriatic - Ανοσοκατασταλτικά - plaque psoriasisskyrizi is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisskyrizi, alone or in combination with methotrexate (mtx), is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). crohn's diseaseskyrizi is indicated for the treatment of adult patients with moderately to severely active crohn's disease who have had an inadequate response to, lost response to, or were intolerant to conventional therapy or a biologic therapy.