Flucelvax Tetra Eiropas Savienība - latviešu - EMA (European Medicines Agency)

flucelvax tetra

seqirus netherlands b.v. - a/darwin/6/2021(h3n2)-like strain (a/darwin/11/2021, wild type) / a/wisconsin/67/2022 (h1n1)pdm09-like strain (a/georgia/12/2022 cvr-167) / b/austria/1359417/2021-like strain (b/singapore/wuh4618/2021) / b/phuket/3073/2013-like virus (b/singapore/inftt-16-0610/2016, wild type) - gripas, cilvēka - gripas vakcīna, inaktivēta, šķelta viriona vai virsmas antigēna - prophylaxis of influenza in adults and children from 2 years of age. flucelvax tetra būtu jāizmanto saskaņā ar oficiālās rekomendācijas.

Fluad Tetra Eiropas Savienība - latviešu - EMA (European Medicines Agency)

fluad tetra

seqirus netherlands b.v. - a/darwin/9/2021 (h3n2) - like strain (a/darwin/6/2021, ivr-227) / a/victoria/4897/2022 (h1n1) pdm09-like strain (a/victoria/4897/2022, ivr-238) / b/phuket/3073/2013-like strain (b/phuket/3073/2013, bvr-1b) / influenza virus b/austria/1359417/2021-like strain (b/austria/1359417/2021, bvr-26) - gripas, cilvēka - vakcīnas - profilakse gripas veci cilvēki (65 gadus veci un vecāki). fluad tetra būtu jāizmanto saskaņā ar oficiālās rekomendācijas.

CircoMax Myco Eiropas Savienība - latviešu - EMA (European Medicines Agency)

circomax myco

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 - imunoloģiskie līdzekļi suidae - cūkas (nobarošanas) - 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.

Eurican DAPPi-Lmulti liofilizāts un suspensija suspensijas injekcijām pagatavošanai Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

eurican dappi-lmulti liofilizāts un suspensija suspensijas injekcijām pagatavošanai

boehringer ingelheim animal health france scs , francija - canine adenovirus type 2, strain dk13, canine distemper virus, strain ba5, canine parvovirus type 2, strain cag2, canine parainfluenza virus type 2, strain cgf 2004/75, leptospira interrogans, serogroup canicola, serovar canicola, strain 16070, inactivated, leptospira interrogans, serogroup icterohaemorrhagiae, serovar icterohaemorrhagiae, strain 16069, inactivated, leptospira interrogans, serogroup grippotyphosa, serovar grippotyphosa, strain grippo mal 1540, inactivated - liofilizāts un suspensija suspensijas injekcijām pagatavošanai - suņi

Zoonotic Influenza Vaccine Seqirus Eiropas Savienība - latviešu - EMA (European Medicines Agency)

zoonotic influenza vaccine seqirus

seqirus s.r.l.  - zoonotic influenza vaccine (h5n1) (surface antigen, inactivated, adjuvanted), influenza virus surface antigens (haemagglutinin and neuraminidase) of strain: a/turkey/turkey/1/05 (h5n1)-like strain (nibrg-23) - influenza a virus, h5n1 subtype - vakcīnas - active immunisation against h5 subtype of influenza a virus.

CREATINE MONOHYDRATE Pulveris Latvija - latviešu - Pārtikas un veterinārais dienests, Zemkopības ministrija

creatine monohydrate pulveris

bellum, sia lv40003202289 artilērijas 13 k.2-20, rīga - pulveris - cits - pārtikas produkts, kas paredzēts intensīvas muskuļu piepūles gadījumos, īpaši sportistiem

Coxevac Eiropas Savienība - latviešu - EMA (European Medicines Agency)

coxevac

ceva santé animale - inaktivēta coxiella burnetii vakcīna, deviņu mile celms - immunologicals for bovidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) - goats; cattle - cattle: , for the active immunisation of cattle to lower the risk for non-infected animals vaccinated when non-pregnant to become shedder (5 times lower probability in comparison with animals receiving a placebo), and to reduce shedding of coxiella burnetii in these animals via milk and vaginal mucus. , onset of immunity: not established. , duration of immunity: 280 days after completion of the primary vaccination course. , goats: , for the active immunisation of goats to reduce abortion caused by coxiella burnetii and to reduce shedding of the organism via milk, vaginal mucus, faeces and placenta. , onset of immunity: not established. , duration of immunity: one year after completion of the primary vaccination course.

Vepured Eiropas Savienība - latviešu - EMA (European Medicines Agency)

vepured

laboratorios hipra, s.a. - e. coli rekombinants verotoksīns 2e - inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) escherichia + clostridium, immunologicals for suidae - cūkas - sivēnu aktīva imunizācija no 2 dienu vecuma, lai novērstu mirstību un samazinātu tūskas slimības klīniskās pazīmes (ko izraisījis e (iegūts ar verotoksīnu 2e). coli) un lai samazinātu ikdienas svara pieauguma zudumu beigu periodā, saskaroties ar infekcijām ar verotoksīnu 2e, kas ražo e. coli līdz nokaušanai no 164 dienu vecumā.

Clopidogrel/Acetylsalicylic acid Teva Eiropas Savienība - latviešu - EMA (European Medicines Agency)

clopidogrel/acetylsalicylic acid teva

teva pharma b.v. - clopidogrel, acetylsalicylic acid - acute coronary syndrome; myocardial infarction - combinations - clopidogrel/acetylsalicylic acid teva indicēts aterotrombotiskām notikumiem pieaugušiem pacientiem, kas jau veic gan clopidogrel acetilsalicilskābes (asa) profilakse. klopidogrelu/acetilsalicilskābe teva ir fiksētas devas kombinācija zāles, turpinot terapiju:bez st segmenta pacēluma akūtu koronāro sindromu (nestabila stenokardija vai ne‑q zoba miokarda infarkts), tostarp pacientiem, kam veic stentu izvietošana pēc perkutānas koronāras interventionst segmenta pacēlums, akūts miokarda infarkts, medicīniski ārstēti pacienti saņemt trombolītiskā terapija.