ESMERON süste-/infusioonilahus Eistland - eistneska - Ravimiamet

esmeron süste-/infusioonilahus

organon n.v. - rokurooniumbromiid - süste-/infusioonilahus - 10mg 1ml 5ml 10tk

REMERON SOLTAB dispergeeruv tablett Eistland - eistneska - Ravimiamet

remeron soltab dispergeeruv tablett

organon n.v. - mirtasapiin - dispergeeruv tablett - 30mg 48tk

Klisyri Evrópusambandið - eistneska - EMA (European Medicines Agency)

klisyri

almirall, s.a. - tirbanibulin - keratoos, actinic - antibiootikumid ja kemoterapeutikumid dermatoloogiliseks kasutamiseks - klisyri is indicated for the field treatment of non-hyperkeratotic, non-hypertrophic actinic keratosis (olsen grade 1) of the face or scalp in adults.

DIPROSALIC salv Eistland - eistneska - Ravimiamet

diprosalic salv

organon heist - beetametasoon+salitsüülhape - salv - 0,5mg+30mg 1g 20g 1tk

Ivabradine JensonR Evrópusambandið - eistneska - EMA (European Medicines Agency)

ivabradine jensonr

jensonr+ limited - ivabradiinvesinikkloriid - angina pectoris; heart failure - südame teraapia - kroonilise stabiilse stenokardia sümptomaatiline ravi koronaararterite haiguse täiskasvanutel normaalse sinusurma ja südame löögisagedusega ≥ 70 löögi minutis. ivabradiin on näidustatud: - täiskasvanutel ei talu või kellel beetablokaatorite - või koos beetablokaatoritega patsientidel, optimaalne beetablokaatoriga annuse kasutamise vastunäidustuse. ravi kroonilise südamepuudulikkuse ivabradiin on näidustatud kroonilise südamepuudulikkuse nyha ii – iv klassi, patsientidel siinusrütm ja kelle pulsisagedus on üle 75 löögi minutis, sealhulgas beetablokaatoriga ravi koos või kuna beetablokaatoriga ravi on vastunäidustatud või mittetalutav.

Opdivo Evrópusambandið - eistneska - EMA (European Medicines Agency)

opdivo

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 - antineoplastilised ained - 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.

Pemetrexed Pfizer (previously Pemetrexed Hospira) Evrópusambandið - eistneska - EMA (European Medicines Agency)

pemetrexed pfizer (previously pemetrexed hospira)

pfizer europe ma eeig - pemetrexed disodium, pemetrexed disodium hemipentahydrate - carcinoma, non-small-cell lung; mesothelioma - antineoplastilised ained - malignant pleural mesotheliomapemetrexed pfizer in combination with cisplatin is indicated for the treatment of chemotherapy naïve patients with unresectable malignant pleural mesothelioma. non-small cell lung cancerpemetrexed pfizer in combination with cisplatin is indicated for the first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology. pemetrexed pfizer is indicated as monotherapy for the maintenance treatment of locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology in patients whose disease has not progressed immediately following platinum-based chemotherapy. pemetrexed pfizer is indicated as monotherapy for the second-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology.

Zuritol suukaudne suspensioon Eistland - eistneska - Ravimiamet

zuritol suukaudne suspensioon

laboratorios calier s.a. - toltrasuriil - suukaudne suspensioon - 50mg 1ml 250ml 1tk; 50mg 1ml 1000ml 1tk

Effinol nahasprei, lahus Eistland - eistneska - Ravimiamet

effinol nahasprei, lahus

laboratorios calier s.a. - fiproniil - nahasprei, lahus - 2,5mg 1ml 500ml 1tk; 2,5mg 1ml 100ml 1tk; 2,5mg 1ml 250ml 1tk

Ceftiomax süstesuspensioon Eistland - eistneska - Ravimiamet

ceftiomax süstesuspensioon

laboratorios calier s.a. - tseftiofuur - süstesuspensioon - 50mg 1ml 100ml 1tk; 50mg 1ml 250ml 1tk