Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

nassington ltd, cyprus Ιπποκράτους 3Α,, 2006 Λευκωσία - benzydamine hydrochloride - vag.sol (ΚΟΛΠΙΚΟ ΔΙΑΛΥΜΑ) - 0.1% (w/v) - benzydamine hydrochloride 0,1% - benzydamine

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

ΙΟΥΛ.& ΕΙΡ. ΤΣΕΤΗ ΦΑΡ/ΚΑ ΕΡΓΑΣΤΗΡΙΑ ΑΒΕΕ Δ.Τ."intermed abee" Καλυφτάκη 27,, 145 64 145 64, Κηφισιά 210-6253904 - ibuprofen lysinate - vag.sol (ΚΟΛΠΙΚΟ ΔΙΑΛΥΜΑ) - 1% w/v - ibuprofen lysinate 10mg - ibuprofen

Κύπρος - Ελληνικά - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

ioulia and irene tseti pharmaceutical laboratories s.a. (0000009807) kalyftaki 27 str., k.kifissia, gr 145 64 - ibuprofen lysinate - ΚΟΛΠΙΚΟ ΔΙΑΛΥΜΑ - 1% w/v - ibuprofen lysinate (0057469779) 10mg - ibuprofen

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

benzydamine hydrochloride - vag.sol (ΚΟΛΠΙΚΟ ΔΙΑΛΥΜΑ) - 0.1% (w/v) - benzydamine hydrochloride 0,1% - benzydamine

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

merial - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated chlamydophila felis (905 strain) - Ανοσολογικά για αιλουροειδών, - Γάτες - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs and excretion;against chlamydophila felis infection to reduce clinical signs. Τα αντισώματα ανοσίας έχουν αποδειχθεί 1 εβδομάδα μετά τον κύριο εμβολιασμό για ρινοτραχειίτιδα, καλυκοϊό και συστατικά chlamydophila felis. Η διάρκεια της ανοσίας είναι 1 έτος μετά τον τελευταίο (επαν) εμβολιασμό.

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

regeneron ireland designated activity company (dac) - cemiplimab - Καρκίνωμα, σκουός κύτταρο - Αντινεοπλασματικοί παράγοντες - cutaneous squamous cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with metastatic or locally advanced cutaneous squamous cell carcinoma (mcscc or lacscc) who are not candidates for curative surgery or curative radiation. basal cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic basal cell carcinoma (labcc or mbcc) who have progressed on or are intolerant to a hedgehog pathway inhibitor (hhi). non-small cell lung cancerlibtayo as monotherapy is indicated for the first-line treatment of adult patients with non-small cell lung cancer (nsclc) expressing pd-l1 (in ≥ 50% tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. libtayo in combination with platinum‐based chemotherapy is indicated for the first‐line treatment of adult patients with nsclc expressing pd-l1 (in ≥ 1% of tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. cervical cancerlibtayo as monotherapy is indicated for the treatment of adult patients with recurrent or metastatic cervical cancer and disease progression on or after platinum-based chemotherapy.

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

merck europe b.v. - avelumab - Νευροενδοκρινικοί όγκοι - Άλλοι αντινεοπλασματικοί παράγοντες, Μονοκλωνικά αντισώματα - Το bavencio ενδείκνυται ως μονοθεραπεία για τη θεραπεία ενηλίκων ασθενών με μεταστατικό καρκίνωμα κυττάρων merkel (mcc). bavencio σε συνδυασμό με axitinib ενδείκνυται για τη θεραπεία πρώτης γραμμής σε ενήλικες ασθενείς με προχωρημένο νεφροκυτταρικό καρκίνωμα (rcc). bavencio is indicated as monotherapy for the first‑line maintenance treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc) who are progression-free following platinum‑based chemotherapy.

Κύπρος - Ελληνικά - Κυπριακή Δημοκρατία, Υπουργείο Γεωργίας, Αγροτικής Ανάπτυξης και Περιβάλλοντος, Κτηνιατρικές Υπηρεσίες

qi02al01 - granted - bioveta a.s. - spyros stavrinides chemicals ltd

Κύπρος - Ελληνικά - Κυπριακή Δημοκρατία, Υπουργείο Γεωργίας, Αγροτικής Ανάπτυξης και Περιβάλλοντος, Κτηνιατρικές Υπηρεσίες

medisell co ltd - inactivated pasteurella multocida, serotype a, strain nctc 12177 and inactivated pasteurella multocida, serotype 6b, strain cect 962 ≥ 104 pd50 * inactivated mannheimia haemolytica, serotype a1, strain atcc 33365 and inactivated mannheimia haemolytica, serotype a2, strain cect 924 ≥ 41.08 ue** - suspension for injection - vaccine - cattle, sheep, goats

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - nivolumab - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; mesothelioma; colorectal neoplasms - Αντινεοπλασματικοί παράγοντες - melanomaopdivo as monotherapy or in combination with ipilimumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older. relative to nivolumab monotherapy, an increase in progression free survival (pfs) and overall survival (os) for the combination of nivolumab with ipilimumab is established only in patients with low tumour pd-l1 expression. adjuvant treatment of melanomaopdivo as monotherapy is indicated for the adjuvant treatment of adults and adolescents 12 years of age and older with melanoma with involvement of lymph nodes or metastatic disease who have undergone complete resection. non-small cell lung cancer (nsclc)opdivo in combination with ipilimumab and 2 cycles of platinum-based chemotherapy is indicated for the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising egfr mutation or alk translocation. opdivo as monotherapy is indicated for the treatment of locally advanced or metastatic non-small cell lung cancer after prior chemotherapy in adults. neoadjuvant treatment of nsclcopdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have pd-l1 expression ≥ 1%. malignant pleural mesothelioma (mpm)opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. neoadjuvant treatment of nsclcopdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have pd-l1 expression ≥ 1%. renal cell carcinoma (rcc)opdivo as monotherapy is indicated for the treatment of advanced renal cell carcinoma after prior therapy in adults. opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with intermediate/poor risk advanced renal cell carcinoma. opdivo in combination with cabozantinib is indicated for the first-line treatment of adult patients with advanced renal cell carcinoma. classical hodgkin lymphoma (chl)opdivo as monotherapy is indicated for the treatment of adult patients with relapsed or refractory classical hodgkin lymphoma after autologous stem cell transplant (asct) and treatment with brentuximab vedotin. squamous cell cancer of the head and neck (scchn)opdivo as monotherapy is indicated for the treatment of recurrent or metastatic squamous cell cancer of the head and neck in adults progressing on or after platinum based therapy. urothelial carcinomaopdivo as monotherapy is indicated for the treatment of locally advanced unresectable or metastatic urothelial carcinoma in adults after failure of prior platinum containing therapy. adjuvant treatment of urothelial carcinomaopdivo as monotherapy is indicated for the adjuvant treatment of adults with muscle invasive urothelial carcinoma (miuc) with tumour cell pd-l1 expression ≥ 1%, who are at high risk of recurrence after undergoing radical resection of miuc. mismatch repair deficient (dmmr) or microsatellite instability-high (msi-h) colorectal cancer (crc)opdivo in combination with ipilimumab is indicated for the treatment of adult patients with mismatch repair deficient or microsatellite instability-high metastatic colorectal cancer after prior fluoropyrimidine based combination chemotherapy. oesophageal squamous cell carcinoma (oscc)opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%. opdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%. opdivo as monotherapy is indicated for the treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma after prior fluoropyrimidine- and platinum-based combination chemotherapy. adjuvant treatment of oesophageal or gastro-oesophageal junction cancer (oc or gejc)opdivo as monotherapy is indicated for the adjuvant treatment of adult patients with oesophageal or gastro-oesophageal junction cancer who have residual pathologic disease following prior neoadjuvant chemoradiotherapy. gastric, gastro‑oesophageal junction (gej) or oesophageal adenocarcinomaopdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy is indicated for the first‑line treatment of adult patients with her2‑negative advanced or metastatic gastric, gastro‑oesophageal junction or oesophageal adenocarcinoma whose tumours express pd-l1 with a combined positive score (cps) ≥ 5.