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Burden of Disease
Burden of Disease
Risk Factors
Secondary Infections
Mechanism of Action
Prevention of Pneumococcal Disease
Need for Pneumococcal Vaccination
Cost-effectiveness of PCV13
Legacy of Prevenar
Safety
Conclusion
Dosing
Prevenar 13® Clinical Experience
Efficacy of Prevenar 13®
Effectiveness of Prevenar 13®
Indian Clinical Trials
Recommendations for Use
PCV13 in Pulmonology
PCV13 in Nephrology
PCV13 in Oncology
PCV13 in Rheumatology
PCV13 in Diabetes
PCV13 in HIV Infection
PCV13 in Cardiology
Resources
The participants (n=84,496), who were 65 years of age or older, were enrolled in the study between 15 September 2008 and 30 January 2010 at 101 community-based sites throughout the Netherlands. Participants were randomly assigned in a 1:1 ratio to receive PCV13 or placebo by intramuscular injection in the right deltoid. The placebo was identical in appearance to PCV13. These participants were followed with home visits for 2 years to obtain additional safety data. All the participants provided written informed consent. During the first 2.5 months of study enrolment, trivalent inactivated influenza vaccine was administered concomitantly with the study vaccine or placebo. About 30.4% of the participants received both vaccines at the vaccination visit.1
PCV13, 13-valent pneumococcal conjugate vaccine.
Reference:
Please click the Prescribing Information link to view the safety and adverse events information of Prevenar 13®.
For the use only of Registered Medical Practitioners or a Hospital or a Laboratory.
PP-PRV-IND-0661 July 2023
Help protect your adult patients against pneumococcal pneumonia with single-dose administration
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Help protect your adult patients against pneumococcal pneumonia with single-dose administration
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The ACIP recommends routine use of PCV13 among adults
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