Unione Europea - italiano - EMA (European Medicines Agency)

amivas ireland ltd - artesunate - malaria - antiprotozoari - artesunate amivas is indicated for the initial treatment of severe malaria in adults and children. dovrebbero essere prese in considerazione le linee guida ufficiali sull'uso appropriato degli agenti antimalarici.

Unione Europea - italiano - EMA (European Medicines Agency)

takeda gmbh - dengue virus, serotype 2, expressing dengue virus, serotype 1, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 3, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 4, surface proteins, live, attenuated, dengue virus, serotype 2, live, attenuated - dengue - vaccini - qdenga is indicated for the prevention of dengue disease in individuals from 4 years of age. the use of qdenga should be in accordance with official recommendations.

Unione Europea - italiano - EMA (European Medicines Agency)

sanofi pasteur - chimeric yellow fever dengue virus serotype 1 (live, attenuated), chimeric yellow fever dengue virus serotype 2 (live, attenuated), chimeric yellow fever dengue virus serotype 3 (live, attenuated), chimeric yellow fever dengue virus serotype 4 (live, attenuated) - dengue - vaccini - dengvaxia is indicated for the prevention of dengue disease caused by dengue virus serotypes 1, 2, 3 and 4 in individuals 6 to 45 years of age with test-confirmed previous dengue infection (see sections 4. 2, 4. 4 e 4. l'uso di dengvaxia dovrebbe essere in conformità con le raccomandazioni ufficiali.

Unione Europea - italiano - EMA (European Medicines Agency)

accord healthcare s.l.u. - caspofungin acetato - candidiasis; aspergillosis - antimicotici per uso sistemico - trattamento della candidiasi invasiva in pazienti adulti o pediatrici. il trattamento dell'aspergillosi invasiva in pazienti adulti o pediatrici, che sono refrattari o intolleranti di amfotericina b, lipidi formulazioni di amfotericina b e/o itraconazolo. la refrattarietà è definito come la progressione di infezione o di mancata migliorare dopo un minimo di 7 giorni prima di dosi terapeutiche di una efficace terapia antimicotica. la terapia empirica per le presunte infezioni da funghi (come la candida o aspergillus) in febbrile, neutropaenic pazienti adulti o pediatrici.

Italia - italiano - Ministero della Salute

demarta virginio di demarta luigia e c. snc - materassi e traverse antidecubito

Unione Europea - italiano - EMA (European Medicines Agency)

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) - prodotti immunologici per felidae, - gatti - 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. insorti di immunità sono stati dimostrati una settimana dopo il corso di vaccinazione primaria per rinotracheite, calicivirus, chlamydophila felis e componenti di panleucopenia. 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.

Unione Europea - italiano - EMA (European Medicines Agency)

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) - prodotti immunologici per felidae, - gatti - 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.

Unione Europea - italiano - EMA (European Medicines Agency)

laboratorios hipra, s.a. - eimeria acervulina, ceppo 003, eimeria maxima, ceppo 013, eimeria mitis, ceppo 006, eimeria precoce, ceppo 007, eimeria tenella, ceppo 004 - live parassitarie, vaccini, prodotti immunologici per uccelli - pollo - per l'immunizzazione attiva dei pulcini di 1 giorno di età per ridurre le lesioni intestinali e oocisti di uscita associati con coccidiosis causato da eimeria acervulina, eimeria maxima, eimeria mitis, eimeria precoce e eimeria tenella e per ridurre i segni clinici (diarrea) associati con eimeria acervulina, eimeria maxima e eimeria tenella.

Unione Europea - italiano - EMA (European Medicines Agency)

merial - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated chlamydophila felis (905 strain) - prodotti immunologici per felidae, - gatti - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs and excretion;against chlamydophila felis infection to reduce clinical signs. insorti di immunità sono stati dimostrati 1 settimana dopo il corso di vaccinazione primaria per componenti di rinotracheite, calicivirus e chlamydophila felis. la durata dell'immunità è di 1 anno dopo l'ultima (ri)vaccinazione.

Unione Europea - italiano - EMA (European Medicines Agency)

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) - prodotti immunologici per felidae, - gatti - 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 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 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 feline leukaemia component, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.