Examples of using Prepandemic in English and their translations into German
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VEPACEL suspension for injection Prepandemic influenza vaccine(H5N1) I. M.
Prepandemic Influenza vaccine(H5N1) surface antigen, inativated, adjuvanted.
Important information about some of the ingredients of Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics.
Prepandemic Influenza vaccine(H5N1) surface antigen, inactivated, adjuvanted.
The studies looked at the ability of the vaccine to trigger the production of antibodies(‘immunogenicity')in line with the CHMP criteria for prepandemic vaccines.
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PREPANDEMIC INFLUENZA VACCINE(H5N1)(SPLIT VIRION, INACTIVATED, ADJUVANTED) GLAXOSMITHKLINE BIOLOGICALS.
If you have previously received one ortwo doses of Prepandrix or Prepandemic influenza vaccine(H5N1)(split virion, inactivated, adjuvanted) GlaxoSmithKline Biologicals 3.75 µg.
What Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics looks like and contents of the pack.
Tell the doctor requesting these tests that you have recently received Prepandemic influenza vaccine(H5N1)(split virion, inactivated, adjuvanted) GlaxoSmithKline Biologicals 3.75 µg.
Pandemic and Prepandemic vaccines contain influenza antigens that are different from those in the currently circulating influenza viruses.
Co-administration was not associated with higher rates of local orsystemic reactions compared to administration of Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics alone.
Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics should be used in accordance with official recommendations.
The potential benefits to the mother andrisks to the infant should be considered before administering Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics during breast-feeding.
A third(booster) dose of Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics was administered 6 months onwards after the primary vaccination.
As soon as the pandemic is declared(Phase6 of the WHO global Influenza preparedness plan) and the prepandemic vaccine is used, the MAH shall submit periodic safety update reports with periodicity and format defined as follows.
Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics is a vaccine for use in adults(from 18 to 60 years old). and elderly over 60 years old.
Data obtained with the H5N1 vaccines will support a vaccination strategy that is likely to be used for the pandemic vaccine: clinical immunogenicity, safety andreactogenicity data obtained with H5N1 vaccines are relevant for the pandemic and prepandemic vaccines.
Up to 50% of the elderly subjects immunised with Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics were seroprotected at six months.
Since Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics is expected not to be used in an emergency situation, its administration during pregnancy might be deferred as a precautionary approach.
Since a second dose is recommended, it should be noted that there are no safety,immunogenicity or efficacy data to support interchangeability of Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics with other H5N1 monovalent vaccines.
Two doses of Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics were administered three weeks apart and a third dose 12 months following the first dose.
In the first few weeks after vaccination with Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics the results of these tests may not be correct.
Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics has been evaluated in healthy adults(18-60 years of age) and healthy elderly(over 60 years of age) following a 1, 22 day primary vaccination schedule, and booster vaccination see sections 4.8 and 5.1.
This section describes the clinical experience with Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics following a two-dose administration and booster.
Therefore the data indicate that Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics may be co-administered with non-adjuvanted seasonal influenza vaccines with injections made into opposite limbs.
In the presence of immune deficiencies Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics may be administered but a protective immune response may not be elicited.
Data on safety of a booster dose of the current Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics formulation are limited to three trials(V87P1, V87P2 and V87P1E1) that included 116 adults and 56 elderly.
Data obtained in adults showed that Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics can be given at the same time as non- adjuvanted seasonal influenza vaccines, with injections made into separate limbs.
Non-clinical data obtained with Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics and with seasonal influenza vaccine containing MF59C.1 adjuvant reveal no special hazard for humans based on conventional studies of repeated dose toxicity, local tolerance, female fertility, and reproductive and developmental toxicity through the end of the lactation period.
A single vaccination with Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics(H5N1, A/Vietnam/1194/2004) induced high and rapid serological response in subjects primed 6-8 years previously with two doses of a different surrogate H5N vaccine, having same formulation as Prepandemic Influenza vaccine(H5N1)(surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics but using the strain H5N3.