Daronrix

Country: European Union

Language: Slovenian

Source: EMA (European Medicines Agency)

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Active ingredient:

Celotno virion, inaktivirano, ki vsebujejo antigen*: A/Vietnam/1194/2004 (H5N1)* proizvedeni v jajca

Available from:

GlaxoSmithKline Biologicals S.A.

ATC code:

J07BB01

INN (International Name):

pandemic influenza vaccine (whole virion, inactivated, adjuvanted)

Therapeutic group:

Cepiva

Therapeutic area:

Influenza, Human; Immunization; Disease Outbreaks

Therapeutic indications:

Preprečevanje gripe v uradno prijavljeni pandemični situaciji. Pandemije gripe cepiva je treba uporabljati v skladu z uradnimi smernice.

Authorization status:

Umaknjeno

Authorization date:

2007-03-21

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 02-07-2013
Summary of Product characteristics Summary of Product characteristics Bulgarian 02-07-2013
Public Assessment Report Public Assessment Report Bulgarian 02-07-2013
Patient Information leaflet Patient Information leaflet Spanish 02-07-2013
Public Assessment Report Public Assessment Report Spanish 02-07-2013
Patient Information leaflet Patient Information leaflet Czech 02-07-2013
Public Assessment Report Public Assessment Report Czech 02-07-2013
Patient Information leaflet Patient Information leaflet Danish 02-07-2013
Public Assessment Report Public Assessment Report Danish 02-07-2013
Patient Information leaflet Patient Information leaflet German 02-07-2013
Public Assessment Report Public Assessment Report German 02-07-2013
Patient Information leaflet Patient Information leaflet Estonian 02-07-2013
Public Assessment Report Public Assessment Report Estonian 02-07-2013
Patient Information leaflet Patient Information leaflet Greek 02-07-2013
Public Assessment Report Public Assessment Report Greek 02-07-2013
Patient Information leaflet Patient Information leaflet English 02-07-2013
Public Assessment Report Public Assessment Report English 02-07-2013
Patient Information leaflet Patient Information leaflet French 02-07-2013
Public Assessment Report Public Assessment Report French 02-07-2013
Patient Information leaflet Patient Information leaflet Italian 02-07-2013
Public Assessment Report Public Assessment Report Italian 02-07-2013
Patient Information leaflet Patient Information leaflet Latvian 02-07-2013
Public Assessment Report Public Assessment Report Latvian 02-07-2013
Patient Information leaflet Patient Information leaflet Lithuanian 02-07-2013
Summary of Product characteristics Summary of Product characteristics Lithuanian 02-07-2013
Public Assessment Report Public Assessment Report Lithuanian 02-07-2013
Patient Information leaflet Patient Information leaflet Hungarian 02-07-2013
Summary of Product characteristics Summary of Product characteristics Hungarian 02-07-2013
Public Assessment Report Public Assessment Report Hungarian 02-07-2013
Public Assessment Report Public Assessment Report Maltese 02-07-2013
Public Assessment Report Public Assessment Report Dutch 02-07-2013
Public Assessment Report Public Assessment Report Polish 02-07-2013
Public Assessment Report Public Assessment Report Portuguese 02-07-2013
Public Assessment Report Public Assessment Report Romanian 02-07-2013
Public Assessment Report Public Assessment Report Slovak 02-07-2013
Patient Information leaflet Patient Information leaflet Finnish 02-07-2013
Public Assessment Report Public Assessment Report Finnish 02-07-2013
Public Assessment Report Public Assessment Report Swedish 02-07-2013

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