Doctor Daniel Nagase, in an exclusive interview with the Western Standard, reviewed recently-released safety data on Pfizer-BioNTech’s COVID-19 vaccine..Nagase came under fire for giving patients an unapproved treatment for COVID-19 while working in Alberta hospitals in September and was banned from working in Alberta Health Services facilities..Public Health and Medical Professionals for Transparency (PHMPT) is a nonprofit organization comprised of public health and medical professionals, scientists and journalists dedicated to “obtain and disseminate the data relied upon by the FDA to license COVID-19 vaccines.” The obtained Pfizer documents are available on the PHMPT website..On August 27, four days after the FDA approved the Pfizer vaccine for ages 16 and up in the US, PHMPT submitted a Freedom of Information Act request to the FDA for all of the data within Pfizer’s COVID-19 vaccine biological product file..The FDA has since released a package of documents to PHMPT including “post-authorization adverse event reports” received through the end of Feb 2021..Please note, when Doctor Nagase references the adverse events in children under 12-years old from the Pfizer data, it is not clear whether the children were injected with an adult dose or pediatric dose..Melanie Risdon is a reporter for the Western Standard.mrisdon@westernstandardonline.com
Doctor Daniel Nagase, in an exclusive interview with the Western Standard, reviewed recently-released safety data on Pfizer-BioNTech’s COVID-19 vaccine..Nagase came under fire for giving patients an unapproved treatment for COVID-19 while working in Alberta hospitals in September and was banned from working in Alberta Health Services facilities..Public Health and Medical Professionals for Transparency (PHMPT) is a nonprofit organization comprised of public health and medical professionals, scientists and journalists dedicated to “obtain and disseminate the data relied upon by the FDA to license COVID-19 vaccines.” The obtained Pfizer documents are available on the PHMPT website..On August 27, four days after the FDA approved the Pfizer vaccine for ages 16 and up in the US, PHMPT submitted a Freedom of Information Act request to the FDA for all of the data within Pfizer’s COVID-19 vaccine biological product file..The FDA has since released a package of documents to PHMPT including “post-authorization adverse event reports” received through the end of Feb 2021..Please note, when Doctor Nagase references the adverse events in children under 12-years old from the Pfizer data, it is not clear whether the children were injected with an adult dose or pediatric dose..Melanie Risdon is a reporter for the Western Standard.mrisdon@westernstandardonline.com
