Purevax RCPCh Uniunea Europeană - română - 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) - produsele imunologice pentru felidae, - pisici - 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. incidența imunității a fost demonstrată la o săptămână după vaccinarea primară pentru rinotraheită, calicivirus, chlamydophila felis și componentele panleucopeniei. 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.

Purevax RCPCh FeLV Uniunea Europeană - română - EMA (European Medicines Agency)

purevax rcpch felv

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated feline panleucopenia virus (pli iv), felv recombinant canarypox virus (vcp97), attenuated chlamydophila felis (905 strain) - produsele imunologice pentru felidae, - pisici - active immunisation of cats aged 8 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;against leukaemia to prevent persistent viraemia and clinical signs of the related disease. onsets of immunity are 1 week after primary vaccination course for rhinotracheitis, calicivirus, chlamydophila felis and panleucopenia components, and 2 weeks after primary vaccination course for feline leukaemia component. the duration of immunity is one year after the last re-vaccination for the chlamydiosis and feline leukaemia components, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Bimervax Uniunea Europeană - română - EMA (European Medicines Agency)

bimervax

hipra human health s.l. - sars-cov-2 virus recombinant spike (s) protein receptor binding domain (rbd) fusion heterodimer – b.1.351-b.1.1.7 strains - covid-19 virus infection - vaccinuri - bimervax is indicated as a booster for active immunisation to prevent covid-19 in individuals 16 years of age and older who have previously received a mrna covid-19 vaccine.

Tiyozid 4 mg comprimate Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

tiyozid 4 mg comprimate

nobel ilac pazarlama ve sanayii ltd. Şti - thiocolchicosidum - comprimate - 4 mg

Tiyozid 8 mg comprimate Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

tiyozid 8 mg comprimate

nobel ilac pazarlama ve sanayii ltd. Şti - thiocolchicosidum - comprimate - 8 mg

Amoxicilin 1 g pulbere pentru soluţie injectabilă/perfuzabilă Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

amoxicilin 1 g pulbere pentru soluţie injectabilă/perfuzabilă

zhuhai united laboratories (zhongshan) co. ltd - kalii - pulbere pentru soluţie injectabilă/perfuzabilă - 1 g

Amoxicilin 500 mg pulbere pentru soluţie injectabilă/perfuzabilă Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

amoxicilin 500 mg pulbere pentru soluţie injectabilă/perfuzabilă

zhuhai united laboratories (zhongshan) co. ltd - kalii - pulbere pentru soluţie injectabilă/perfuzabilă - 500 mg

Bekaljin pulbere si solvent pentru solutie injectabila 1000 mg Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

bekaljin pulbere si solvent pentru solutie injectabila 1000 mg

mustafa nevzat ilac sanayii a.s. - cefotaximum - pulbere si solvent pentru solutie injectabila - 1000 mg

ORTANOL 40 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

ortanol 40 mg

lek pharmaceuticals d.d. - slovenia - omeprazolum - caps. gastrorez. - 40mg - med. pt. trat. ulcerului gastro-duodenal si bolii-reflux g.e inhibitori ai pompei de protoni

SIMVAHEXAL 10 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

simvahexal 10 mg

hexal ag - simvastatinum - compr. film. - 10mg - hipocolesterolemiante si hipotrigliceridemiante inhibitori ai hmg coa reductazei