Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

le vet b.v. - prednisolone - kortikosteroīdi sistēmiskai lietošanai, vienkāršā, prednizolons, sistēmisko hormonālo preparātu, bez pvn). dzimumhormonus un insulīnu - zirgi - iekaisuma un klīnisko parametru, kas saistīti ar recidivējošu elpceļu obstrukciju (rao), atvieglojums zirgiem kopā ar vides kontroli.

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

eli lilly and company limited  - fentanyl - nervu sistēma - suņi - lai kontrolētu sāpes, kas saistītas ar ortopēdisku un mīksto audu operācijām suņiem.

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

le vet beheer b.v. - dexmedetomidine hydrochloride - psycholeptics, hypnotics un sedatīviem - neinvazīva, nedaudz līdz mēreni sāpīgi, procedūrām un pārbaudēm, kuras prasa savaldību, narkozes un pretsāpju suņiem un kaķiem. dziļas narkozes un pretsāpju suņiem, jo vienlaicīga lietošana ar butorfanols medicīnas un nelielas ķirurģiskas procedūras,. premedikācija suņiem un kaķiem pirms vispārējās anestēzijas ievadīšanas un uzturēšanas.

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

warner chilcott uk ltd. - testosterons - seksuālās disfunkcijas, psiholoģiskā - dzimumhormoni un dzimumsistēmas modulatori dzimumorgānu sistēma, - intrinsa hypoactive seksuālo vēlmi traucējumi (hsdd) ārstēšanai tiek norādīta abpusēji oophorectomised un hysterectomised (ķirurģiski izraisītas menopauzes) sievietes saņem vienlaicīga estrogēnu terapiju.

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

merck sharp & dohme b.v. - fosaprepitants - vomiting; cancer - pretvemšanas un antinauseants, - profilakses, slikta dūša un vemšana, kas saistīta ar augsti un vidēji emetogenic vēža ķīmijterapija pieaugušajiem un pediatrijas pacienti vecumā no 6 mēneši un vecāki. ivemend 150 mg ir sniegta kā daļa no terapijas kombinācija.

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

merck sharp & dohme b.v. - sitagliptin, metformīns hidrohlorīds - cukura diabēts, 2. tips - cukura diabēts - pacientiem ar 2. tipa cukura diabētu:janumet ir norādīts kā palīglīdzekli, lai diētu un vingrinājumiem, lai uzlabotu glycaemic kontroles pacientiem nepietiekami kontrolē par to maksimālā pieļaujama devu metformīns atsevišķi vai tām, kas jau tiek ārstēti ar kombināciju sitagliptin un metformīns. janumet ir norādīts kombinācijā ar sulfonilurīnvielas pamata, (es. , triple kombinēto terapiju), kā palīglīdzekli, lai diētu un vingrošanu pacientiem nepietiekami kontrolē par to maksimālā pieļaujama devu metformīns un sulfonilurīnvielas pamata. janumet ir norādīts kā triple kombinēto terapiju ar ppar agonistu (i. , thiazolidinedione) kā palīglīdzekli, lai diētu un vingrošanu pacientiem nepietiekami kontrolē par to maksimālā pieļaujama devu metformīns un ppar agonistu. janumet ir arī norādīts, kā pievienot uz insulīna i. , triple kombinēto terapiju), kā palīglīdzekli, lai diētu un vingrinājumiem, lai uzlabotu glycaemic kontroles pacientiem, ja tās ir stabilas devas insulīna un metformīns vien nenodrošina pietiekamu kontroles glycaemic.

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

merck sharp and dohme b.v - sitagliptin - cukura diabēts, 2. tips - cukura diabēts - pieaugušiem pacientiem ar 2. tipa cukura diabētu, januvia ir norādīts, lai uzlabotu glycaemic kontrole:kā monotherapy:pacientiem nepietiekami kontrolēts ar diētu un vingrošanu, vieni un kuriem metformīns ir nevietā, jo kontrindikācijas vai nepanesamību;kā dual dobuma terapija kombinācijā ar:metformīns, kad diētu un vingrošanu, plus metformīns vien nenodrošina pietiekamu glycaemic kontrole;sulfonilurīnvielas pamata, kad diētu un vingrošanu, plus maksimālā pieļaujama devu sulfonilurīnvielas pamata, vien nenodrošina pietiekamu glycaemic kontroli un, ja metformīns ir nevietā, jo kontrindikācijas vai neiecietība;a peroxisome-proliferator aktivizēts receptoru-gamma (ppary) agonistu (i. a thiazolidinedione), kad izmantot ppary agonistu ir gadījumā un tad, ja diēta un fiziskā plus ppary agonistu vien nenodrošina pietiekamu glycaemic kontrole;ppary agonistu (i. a thiazolidinedione), kad izmantot ppary agonistu ir gadījumā un tad, ja diēta un fiziskā plus ppary agonistu vien nenodrošina pietiekamu glycaemic kontroli;kā triple dobuma terapija kombinācijā ar sulfonilurīnvielas pamata, un metformīns, kad diētu un vingrošanu, plus dual terapija ar šīm zālēm nesniedz pienācīgu glycaemic kontrole;ppary agonists un metformīns, kad izmantot ppary agonistu ir gadījumā un tad, ja diēta un fiziskā plus dual terapija ar šīm zālēm nesniedz pienācīgu glycaemic kontrole. januvia ir arī norādīts, kā add-on, lai insulīnu (ar vai bez metformīns) tad, ja diēta un fiziskā plus stabilu devu insulīna nenodrošina pietiekamu kontroles glycaemic.

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

merck sharp & dohme b.v. - pembrolizumabs - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; endometrial neoplasms - antineoplastiski līdzekļi - melanomakeytruda as monotherapy is indicated for the treatment of adults and adolescents aged 12 years and older with advanced (unresectable or metastatic) melanoma. keytruda as monotherapy is indicated for the adjuvant treatment of adults and adolescents aged 12 years and older with stage iib, iic, or with stage iii melanoma and lymph node involvement who have undergone complete resection. non small cell lung carcinoma (nsclc)keytruda as monotherapy is indicated for the adjuvant treatment of adults with non-small cell lung carcinoma who are at high risk of recurrence following complete resection and platinum based chemotherapy (for selection criteria, see section 5. keytruda as monotherapy is indicated for the first line treatment of metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 50% tumour proportion score (tps) with no egfr or alk positive tumour mutations. keytruda, in combination with pemetrexed and platinum chemotherapy, is indicated for the first-line treatment of metastatic non squamous non small cell lung carcinoma in adults whose tumours have no egfr or alk positive mutations. keytruda, in combination with carboplatin and either paclitaxel or nab paclitaxel, is indicated for the first line treatment of metastatic squamous non small cell lung carcinoma in adults. keytruda  as monotherapy is indicated for the treatment of locally advanced or metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 1% tps and who have received at least one prior chemotherapy regimen. pacientiem ar egfr vai bĀziskĀ pozitīvas mutācijas audzēja arī būtu saņēmuši mērķtiecīgu terapiju, pirms saņem keytruda. classical hodgkin lymphoma (chl)keytruda as monotherapy is indicated for the treatment of adult and paediatric patients aged 3 years and older with relapsed or refractory classical hodgkin lymphoma who have failed autologous stem cell transplant (asct) or following at least two prior therapies when asct is not a treatment option. urothelial carcinomakeytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who have received prior platinum containing chemotherapy. keytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who are not eligible for cisplatin containing chemotherapy and whose tumours express pd l1 with a combined positive score (cps) ≥ 10. head and neck squamous cell carcinoma (hnscc)keytruda, as monotherapy or in combination with platinum and 5 fluorouracil (5 fu) chemotherapy, is indicated for the first line treatment of metastatic or unresectable recurrent head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a cps ≥ 1. keytruda as monotherapy is indicated for the treatment of recurrent or metastatic head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a ≥ 50% tps and progressing on or after platinum containing chemotherapy. renal cell carcinoma (rcc)keytruda, in combination with axitinib, is indicated for the first line treatment of advanced renal cell carcinoma in adults. keytruda  as monotherapy is indicated for the adjuvant treatment of adults with renal cell carcinoma at increased risk of recurrence following nephrectomy, or following nephrectomy and resection of metastatic lesions (for selection criteria, please see section 5. microsatellite instability high (msi-h) or mismatch repair deficient (dmmr) cancerscolorectal cancer (crc)keytruda as monotherapy is indicated for theadults with msi-h or dmmr colorectal cancer in the following settings:first line treatment of metastatic microsatellite instability high (msi h) or mismatch repair deficient (dmmr) colorectal cancer in adults;treatment of unresectable or metastatic colorectal cancer after previous fluoropyrimidine based combination therapy.  non-colorectal cancerskeytruda as monotherapy is indicated for the treatment of the following msi h or dmmr tumours in adults with:advanced or recurrent endometrial carcinoma, who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation;unresectable or metastatic gastric, small intestine, or biliary cancer, who have disease progression on or following at least one prior therapy. oesophageal carcinomakeytruda, in combination with platinum and fluoropyrimidine based chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic carcinoma of the oesophagus or her-2 negative gastroesophageal junction adenocarcinoma, in adults whose tumours express pd l1 with a cps ≥ 10. triple negative breast cancer (tnbc)keytruda, in combination with chemotherapy as neoadjuvant treatment, and then continued as monotherapy as adjuvant treatment after surgery, is indicated for the treatment of adults with locally advanced, or early stage triple negative breast cancer at high risk of recurrence. keytruda, in combination with chemotherapy, is indicated for the treatment of locally recurrent unresectable or metastatic triple negative breast cancer in adults whose tumours express pd l1 with a cps ≥ 10 and who have not received prior chemotherapy for metastatic disease. endometrial carcinoma (ec)keytruda, in combination with lenvatinib, is indicated for the treatment of advanced or recurrent endometrial carcinoma in adults who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation. cervical cancerkeytruda, in combination with chemotherapy with or without bevacizumab, is indicated for the treatment of persistent, recurrent, or metastatic cervical cancer in adults whose tumours express pd l1 with a cps ≥ 1. gastric or gastro-oesophageal junction (gej) adenocarcinomakeytruda, in combination with trastuzumab, fluoropyrimidine and platinum-containing chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic her2-positive gastric or gastro-oesophageal junction adenocarcinoma in adults whose tumours express pd-l1 with a cps ≥ 1.

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

warner chilcott  deutschland gmbh - testosterons - seksuālās disfunkcijas, psiholoģiskā - dzimumhormoni un dzimumsistēmas modulatori dzimumorgānu sistēma, - livensa hypoactive seksuālo vēlmi traucējumi (hsdd) ārstēšanai tiek norādīta abpusēji oophorectomised un hysterectomised (ķirurģiski izraisītas menopauzes) sievietes saņem vienlaicīga estrogēnu terapiju.

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

baxalta innovations gmbh - susoctocog alfa - a hemofīlija - antihemorāģija - asiņošanas epizožu ārstēšana pacientiem ar iegūto hemofiliju, ko izraisa antivielas pret viii faktoru. obizur ir indicēts pieaugušajiem.