Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

hra pharma rare diseases - metiraponas - minkštosios kapsulės - 250 mg - metyrapone

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

accord healthcare b.v. - mikofenolato mofetilis - plėvele dengtos tabletės - 500 mg - mycophenolic acid

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

teva pharma b.v. - mikofenolato mofetilis - dantų atmetimas - imunosupresantai - mikofenolato mofetilio teva skirtas vartoti kartu su ciklosporinu ir kortikosteroidais transplantato ūminio atmetimo profilaktikai pacientams, vartojantiems alogeninės inkstų, širdies ar kepenų transplantacijos.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

zoetis belgium - inactivated mycoplasma hyopneumoniae, strain p-5722-3, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2a open reading frame 2 (orf2) protein, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2b orf2 protein - imunologiniai vaisiai suidae - kiaulių (mėsiniai) - active immunisation of pigs against porcine circovirus type 2 to reduce viral load in blood and lymphoid tissues, fecal shedding and the lesions in lymphoid tissues associated with pcv2 infection. protection was demonstrated against porcine circovirus types 2a, 2b and 2d. active immunisation of pigs against mycoplasma hyopneumoniae to reduce the lung lesions associated with mycoplasma hyopneumoniae infection.  onset of immunity (both vaccination schedules): 3 weeks after (the last) vaccination.  duration of immunity (both vaccination schedules): 23 weeks after (the last) vaccination.  in addition, vaccination has been shown to reduce body weight gain losses under field conditions.

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

ranbaxy uk ltd. - mikofenolato mofetilis - plėvele dengtos tabletės - 500 mg - mycophenolic acid

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

actiofarma, uab - mikofenolato mofetilis - plėvele dengtos tabletės - 500 mg - mycophenolic acid

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

lex ano, uab - mikofenolato mofetilis - plėvele dengtos tabletės - 500 mg - mycophenolic acid

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

pharmsure veterinary products europe ltd - mycoplasma synoviae štamas ms-h - immunologicals už ave, gyventi bakterinės vakcinos - vištiena - aktyvios imunizacijos ateityje broilerių veisėjas viščiukų, ateityje sluoksnis veisėjas viščiukų ir ateityje sluoksnis viščiukų sumažinti oro maišelį, pakitimai ir sumažinti kiaušinių skaičius, kurių sutrikusi korpuso formavimas sukelia mycoplasma synoviae.

Europos Sąjunga - lietuvių - 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 - kiaulės - 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.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - pegcetacoplan - hemoglobinurija, paroksizminis - imunosupresantai - aspaveli is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh) who are anaemic after treatment with a c5 inhibitor for at least 3 months.