Prevnar 13 فايزر ::
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PREVNAR 13 pneumococcal 13-valent conjugate vaccine [diphtheria CRM197 Protein] This product information is intended only for residents of the United States. for Health Care Professionals: PREVNAR 13 U.S. Physician Prescribing Information. Prevnar 13 is not FDA-approved for patients 6 through 49 years of age. Pfizer is conducting a variety of clinical studies using Prevnar 13 in immunocompromised individuals and expects results at the end of 2012 and into 2013. Data on the safety and effectiveness of Prevnar 13 when administered to immunocompromised individuals are not available. Prevnar 13 ® is a vaccine indicated for active immunization for the prevention of disease caused by Streptococcus pneumoniae serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, and 23F; In children 6 weeks through 17 years for invasive disease caused by the 13 serotypes, and for children 6 weeks through 5 years of age for otitis media caused by 7 of the 13 serotypes only 4, 6B, 9V, 14. For more information on PREVNAR 13 please click here.Canadian regulations limit the scope of information we are permitted to give on prescription drugs via the Internet or other means. Please consult a qualified health professional for more detailed information.Please contact Pfizer Canada Medical Information at 1 800 463-6001 with any comments or inquiries.

The effectiveness of Prevnar 13 in this specific population has not been established. In an open-label, single-arm, descriptive study, 3 doses of Prevnar 13 were administered 1 month apart to HIV-infected subjects ≥6 years of age with CD4 counts ≥200 cells/µL, and serum HIV RNA titer <50,000 copies/mL. BUSINESS WIRE--Pfizer Inc. NYSE:PFE announced today that data from a Phase 3 study of Prevnar 13® Pneumococcal 13-valent Conjugate Vaccine [Diphtheria CRM197 Protein] met all study endpoints, showing immunogenicity and establishing a safety profile in children and adolescents aged 5 through 17 years. These data, which are being presented today during the 8th. Prevnar® 13 Pneumococcal 13-valent Conjugate Vaccine Product Monograph Page 6of 61 Pediatrics: The safety and immunogenicity of Prevnar 13 in children below the age of 6 weeks have not been established. Geriatrics: Prevnar 13 has been studied in the. BUSINESS WIRE--Pfizer Inc. NYSE:PFE today announced that the data from its two pivotal Phase 3 immunogenicity and safety trials of Prevnar 13® Pneumococcal 13-valent Conjugate Vaccine [Diphtheria CRM197 Protein] in adults aged 50 years and older met all study endpoints. These studies provide the clinical foundation for the regulatory filings that have been submitted in. Prevnar 13 can also be given concomitantly with the tetanus toxoid conjugated meningococcal polysaccharide serogroups A, C, W and Y vaccine, administered between 12-23 months of age in children who have previously received the infant series of Prevnar 13 see PART II, CLINICAL TRIALS section.

10/01/41 · Pfizer's experimental pneumococcal vaccine has shown early clinical success in healthy infants, supporting the company's plans to advance the Prevnar 13 successor into Phase 3 testing, the pharma said Monday. Since 2014, Prevnar 13 has brought in. Prevnar 13, Pneumococcal 13-valent Conjugate Vaccine Diphtheria CRM 197 Protein is a sterile suspension of saccharides of the capsular antigens of Streptococcus pneumoniae serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, and 23F, individually linked to non-toxic diphtheria CRM 197 protein. Each serotype is grown in soy peptone broth.

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