Abstract

Summary The purified inactivated Pasteur rabies vaccine was prepared on primary culture of foetal bovine kidney cells using the Pasteur fixed rabies virus (PV). A clinical trial in a post-exposure situation was carried out on a group of 130 volunteers. The vaccine was administered according to the WHO scheme for vaccines prepared on human diploid cells: 4 injections of 1.0 ml on days 0, 3, 7 and 14, followed by booster doses on days 30 and 90. This induced the production of neutralizing antibodies, detected from day 14. Neither local nor systemic adverse reactions of any importance were registered.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.