SANDOSTATIN LAR süstesuspensiooni pulber ja lahusti Estonia - Esti - Ravimiamet

sandostatin lar süstesuspensiooni pulber ja lahusti

novartis baltics sia - oktreotiid - süstesuspensiooni pulber ja lahusti - 10mg 3tk; 10mg 1tk

SANDIMMUN NEORAL pehmekapsel Estonia - Esti - Ravimiamet

sandimmun neoral pehmekapsel

novartis baltics sia - tsüklosporiin - pehmekapsel - 50mg 50tk

Enerzair Breezhaler Uni Eropa - Esti - EMA (European Medicines Agency)

enerzair breezhaler

novartis europharm limited - indacaterol, glycopyrronium bromide, mometasone - astma - ravimid hingamisteede obstruktiivsete haiguste, - enerzair breezhaler is indicated as a maintenance treatment of asthma in adult patients not adequately controlled with a maintenance combination of a long acting beta2 agonist and a high dose of an inhaled corticosteroid who experienced one or more asthma exacerbations in the previous year.

Zimbus Breezhaler Uni Eropa - Esti - EMA (European Medicines Agency)

zimbus breezhaler

novartis europharm limited - glycopyrronium bromide, indacaterol (acetate), mometasone furoate - astma - ravimid hingamisteede obstruktiivsete haiguste, - maintenance treatment of asthma in adults whose disease is not adequately controlled.

Locametz Uni Eropa - Esti - EMA (European Medicines Agency)

locametz

novartis europharm limited  - gozetotide - radionukliidi pildistamine - diagnostilised radiofarmatseutilised ühendid - see ravim on mõeldud ainult diagnostiliseks kasutamiseks. locametz, after radiolabelling with gallium 68, is indicated for the detection of prostate specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high risk pca prior to primary curative therapy,suspected pca recurrence in patients with increasing levels of serum prostate specific antigen (psa) after primary curative therapy,identification of patients with psma positive progressive metastatic castration resistant prostate cancer (mcrpc) for whom psma targeted therapy is indicated (see section 4.

Pluvicto Uni Eropa - Esti - EMA (European Medicines Agency)

pluvicto

novartis europharm limited  - lutetium (177lu) vipivotide tetraxetan - prostatic kasvajad, kastreerimine-vastupidavad - terapeutilised radiofarmatseutilised ühendid - pluvicto in combination with androgen deprivation therapy (adt) with or without androgen receptor (ar) pathway inhibition is indicated for the treatment of adult patients with progressive prostate-specific membrane antigen (psma)-positive metastatic castration-resistant prostate cancer (mcrpc) who have been treated with ar pathway inhibition and taxane based chemotherapy.

Tevimbra Uni Eropa - Esti - EMA (European Medicines Agency)

tevimbra

novartis europharm limited - tislelizumab - esophageal squamous cell carcinoma - antineoplastilised ained - oesophageal squamous cell carcinoma (oscc) tevimbra as monotherapy is indicated for the treatment of adult patients with unresectable, locally advanced or metastatic oesophageal squamous cell carcinoma after prior platinum-based chemotherapy.

FORADIL AEROLIZER inhalatsioonipulber kõvakapslis Estonia - Esti - Ravimiamet

foradil aerolizer inhalatsioonipulber kõvakapslis

sandoz pharmaceuticals d.d. - formoterool - inhalatsioonipulber kõvakapslis - 12mcg 30tk

Aclasta Uni Eropa - Esti - EMA (European Medicines Agency)

aclasta

sandoz pharmaceuticals d.d. - zoledroonhape - osteoporosis; osteitis deformans; osteoporosis, postmenopausal - narkootikumid luuhaiguste raviks - treatment of osteoporosis: , in post-menopausal women;, in men; , at increased risk of fracture, including those with a recent low-trauma hip fracture. ravi osteoporoosi seotud pikaajalise süsteemse glükokortikoidi ravi post-menopausis naistel ja meestel suurenenud risk luumurdude. ravi paget tõbi, luu.

Atriance Uni Eropa - Esti - EMA (European Medicines Agency)

atriance

sandoz pharmaceuticals d.d. - nelarabiin - prekursori t-rakuline lümfoblastiline leukeemia-lümfoom - antineoplastilised ained - nelarabine on näidustatud ravi patsientidel, kellel on t-rakulise ägeda lümfoblastilise leukeemia (t-all) ja t-rakkude lümfoblastilise lümfoom (t-lbl), kelle haigus ei ole vastanud või on taastekkinud pärast ravi vähemalt kaks keemiaravi raviliikide. due to the small patient populations in these disease settings, the information to support these indications is based on limited data.