Purevax RCPCh Umoja wa Ulaya - Kislovenia - EMA (European Medicines Agency)

purevax rcpch

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated chlamydophila felis (905 strain), attenuated feline panleucopenia virus (pli iv) - immunologicals za skupin felidae, - mačke - active immunisation of cats aged eight weeks and older:• against feline viral rhinotracheitis to reduce clinical signs;• against calicivirus infection to reduce clinical signs;• against chlamydophila felis infection to reduce clinical signs;• against feline panleucopenia to prevent mortality and clinical signs. nastopi imunosti so dokazali en teden po primarno cepljenje seveda za rhinotracheitis, calicivirus, chlamydophila felis in panleucopenia komponente. the duration of immunity is one year after the last re-vaccination for the chlamydiosis component, and oneyear after primary vaccination and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Vaxelis Umoja wa Ulaya - Kislovenia - EMA (European Medicines Agency)

vaxelis

mcm vaccine b.v. - davica toxoid, tetanus toxoid, bordetella oslovskemu kašlju antigenov: oslovskemu kašlju toxoid, nitastih haemagglutinin, pertactin, fimbriae vrste 2 in 3, hepatitis b surface antigen, proizvedene v kvas celice, poliovirus (inaktivirano): tip 1 (mahoney), tip 2 (mef-1), tip 3 (saukett), ki v chicagu celic/ haemophilus influenzae tipa b polysaccharide (polyribosylribitol fosfat) konjugiran na meningococcal beljakovin. - meningitis, haemophilus; poliomyelitis; tetanus; diphtheria; whooping cough; hepatitis b - cepiva - vaxelis (dtap-hb-ipv-hib) je indicirano za osnovno in obnovitveno cepljenje pri dojenčkih in malčkih od starosti 6 tednov, proti davici, tetanus, oslovski kašelj, hepatitis b, otroški ohromelosti in invazivnih bolezni, ki povzroča haemophilus influenzae tipa b (hib). uporaba zdravila vaxelis mora biti v skladu z uradnimi priporočili.

Zinbryta Umoja wa Ulaya - Kislovenia - EMA (European Medicines Agency)

zinbryta

biogen idec ltd - daclizumab - multiple skleroza - imunosupresivi - zdravilo zinbryta je indicirano pri odraslih bolnikih za zdravljenje recidivnih oblik multiple skleroze (rms).

IMIGRAN 6 mg/0,5 ml raztopina za injiciranje Slovenia - Kislovenia - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

imigran 6 mg/0,5 ml raztopina za injiciranje

gsk d.o.o., ljubljana - sumatriptan - raztopina za injiciranje - sumatriptan 6 mg / 0,5 ml - sumatriptan

Reactin 10 mg mehke kapsule Slovenia - Kislovenia - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

reactin 10 mg mehke kapsule

mcneil products limited, foundation park, roxborough way - cetirizin - kapsula, mehka - cetirizin 8,4 mg / 1 kapsula - cetirizin

REGAINE 50 mg/g dermalna pena Slovenia - Kislovenia - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

regaine 50 mg/g dermalna pena

mcneil products limited, foundation park, roxborough way - minoksidil - dermalna pena - minoksidil 50 mg / 1 g - minoksidil

Hexpectoral z okusom mentola 20 mg/ml peroralna raztopina Slovenia - Kislovenia - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

hexpectoral z okusom mentola 20 mg/ml peroralna raztopina

mcneil products limited, foundation park, roxborough way - gvaifenezin - peroralna raztopina - gvaifenezin 20 ml / 1 ml - gvaifenezin

Meropenem Hospira 1000 mg prašek za raztopino za injiciranje ali infundiranje Slovenia - Kislovenia - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

meropenem hospira 1000 mg prašek za raztopino za injiciranje ali infundiranje

hospira uk ltd. - meropenem - prašek za raztopino za injiciranje/infundiranje - meropenem 1000 mg / 1 viala - meropenem