Եվրոպական Միություն - լատվիերեն - EMA (European Medicines Agency)

eli lilly nederland b.v. - glucagon - cukura diabēts - aizkuņģa dziedzera hormoni, hormoni glycogenolytic - baqsimi ir indicēts, lai ārstētu smagas hipoglikēmijas pieaugušajiem, pusaudžiem un bērniem vecumā no 4 gadiem un vairāk, ar cukura diabēts.

Եվրոպական Միություն - լատվիերեն - EMA (European Medicines Agency)

eli lilly nederland b.v. - insulin lispro - cukura diabēts - cukura diabēts - attieksme pret cukura diabētu, pieaugušie, pusaud iem un bērniem vecumā no 1 gada un jaunākām versijām. cukura diabēta ārstēšana pieaugušajiem.

Եվրոպական Միություն - լատվիերեն - EMA (European Medicines Agency)

laboratorios hipra, s.a. - mycoplasma hyopneumoniae, strain 7304 (nexhyon), expressing the capsid protein of porcine circovirus type 2a, inactivated - immunologicals for suidae, inactivated viral and inactivated bacterial vaccines - cūkas - for the active immunisation of pigs:to reduce lung lesions associated with porcine enzootic pneumonia caused by mycoplasma hyopneumoniae. also, to reduce the incidence of these lesions (as observed in field studies). to reduce viraemia, virus load in lungs and lymphoid tissues and the duration of the viraemic period associated with diseases caused by porcine circovirus type 2 (pcv2). efficacy against pcv2 genotypes a, b and d has been demonstrated in field studies. to reduce culling rate and the loss of daily weight gain caused by mycoplasma hyopneumoniae and/or pcv2 related diseases (as observed at 6 months of age in field studies). mycoplasma hyopneumoniae: onset of immunity: 3 weeks after vaccinationduration of immunity: 23 weeks after vaccinationporcine circovirus type 2:onset of immunity: 2 weeks after vaccinationduration of immunity: 22 weeks after vaccinationin addition, a reduction in nasal and faecal shedding and the duration of nasal excretion of pcv2 was demonstrated in animals challenged at 4 weeks and at 22 weeks after vaccination.

Եվրոպական Միություն - լատվիերեն - EMA (European Medicines Agency)

eli lilly nederland b.v. - selpercatinib - carcinoma, non-small-cell lung; thyroid neoplasms - antineoplastiski līdzekļi - retsevmo as monotherapy is indicated for the treatment of adults and adolescents 12 years and older with advanced ret-mutant medullary thyroid cancer (mtc)advanced ret fusion-positive non-small cell lung cancer (nsclc) not previously treated with a ret inhibitoradvanced ret fusion-positive thyroid cancer who require systematic therapy following prior treatment.

Եվրոպական Միություն - լատվիերեն - EMA (European Medicines Agency)

bioprojet pharma - pitolisant - sleep apnea, obstructive - other nervous system drugs - ozawade is indicated to improve wakefulness and reduce excessive daytime sleepiness (eds) in adult patients with obstructive sleep apnoea (osa).

Եվրոպական Միություն - լատվիերեն - EMA (European Medicines Agency)

laboratorios hipra, s.a. - clostridioides difficile toxoid a, clostridioides difficile toxoid b, clostridium perfringens, type a, alpha toxoid - immunologicals for suidae, inactivated bacterial vaccines for pigs, clostridium - cūkas - for the passive immunisation of neonatal piglets by means of the active immunisation of breeding sows and gilts:- to prevent mortality and reduce clinical signs and macroscopic lesions caused by clostridioides difficile toxins a and b. - to reduce clinical signs and macroscopic lesions caused by clostridium perfringens type a, alpha toxin.

Եվրոպական Միություն - լատվիերեն - EMA (European Medicines Agency)

eli lilly nederland b.v. - tirzepatide - cukura diabēts, 2. tips - cukura diabēts - mounjaro is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance or contraindications- in addition to other medicinal products for the treatment of diabetes. for study results with respect to combinations, effects on glycaemic control and the populations studied, see sections 4. 4, 4. 5 un 5.

Եվրոպական Միություն - լատվիերեն - EMA (European Medicines Agency)

eli lilly nederland b.v. - lasmiditan succinate - migrēnas traucējumi - pretsāpju līdzekļi - rayvow is indicated for the acute treatment of the headache phase of migraine attacks, with or without aura in adults.

Եվրոպական Միություն - լատվիերեն - EMA (European Medicines Agency)

samsung bioepis nl b.v. - ekulizumabs - hemoglobīnūrija, paroksizmāla - imūnsupresanti - epysqli is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (pnh). evidence of clinical benefit is demonstrated in patients with haemolysis with clinical symptom(s) indicative of high disease activity, regardless of transfusion history.

Եվրոպական Միություն - լատվիերեն - EMA (European Medicines Agency)

les laboratoires servier - ivosidenib - leukemia, myeloid, acute; cholangiocarcinoma - antineoplastiski līdzekļi - tibsovo in combination with azacitidine is indicated for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (aml) with an isocitrate dehydrogenase-1 (idh1) r132 mutation who are not eligible to receive standard induction chemotherapy (see section 5. tibsovo monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with an idh1 r132 mutation who were previously treated by at least one prior line of systemic therapy.