Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics
·
- Prescription status not stated
- Antibiotics, antivirals and antifungals taken into the body
- Made by
- Novartis Vaccines and Diagnostics S.r.l.
- Source
- Official label
Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.
What it is for
- Active immunisation against H5N1 subtype of Influenza A virus. This indication is based on immunogenicity data from healthy subjects from the age of 18 years onwards following administration of two doses of the vaccine containing A/Vietnam/1194/2004 (H5N1)-like strain. Prepandemic influenza vaccine (H5N1) Novartis Vaccines and Diagnostic should be used in accordance with official recommendations.
From the official label · 2026-09-30 · European Medicines Agency
Same active substance, strength and form in other countries
Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.
Medicine passport: one printable page to show a pharmacist abroad
BulgariaNo exact match for this strength and form
SpainNo exact match for this strength and form
CanadaNo exact match for this strength and form
NetherlandsNo exact match for this strength and form
SwitzerlandNo exact match for this strength and form
Details
| Made by | Novartis Vaccines and Diagnostics S.r.l. |
|---|---|
| Active substance | Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) |
| Used in | Antibiotics, antivirals and antifungals taken into the body |
| Classification | J07BB02 · Antibiotics, antivirals and antifungals taken into the body |
| Authorised on | 2010-11-29 |
| Last updated by the regulator | 2016-03-07 |
| EMA product number | EMEA/H/C/002269 |
Source: European Medicines Agency — medicine data · 2026-09-30 · not reviewed by a clinician
Source: European Medicines Agency (EMA). Product information as published by EMA. Reuse terms: EMA legal notice (reproduction authorised).