Currently there are four major pharmaceutical companies who manufacture a SARS-CoV-2 now called SARS-CoV-19 vaccine. These manufactures and their vaccine are Pfizer–BioNTech mRNA Vaccine, the Moderna-Lonza mRNA-1273 Vaccine, the Serum Institute Oxford Astrazeneca Vaccine and the Janssen COVID -19 Vaccine, manufactured by Janssen Biotech Inc., a Janssen Pharmaceutical Company of Johnson & Johnson, a recombinant, replication-incompetent adenovirus type 26 expressing the SARS-CoV-2 spike protein. The intended purpose of these vaccines are to provide immunity from the so-called infectious novel coronavirus or SARS-CoV – 2 virus now called the SARS-CoV – 19. These four pharmaceutical companies have not provided complete FDA disclosure on their vaccine box, insert fact sheet or label for many of the major and/or minor ingredients contained within these so-called vaccines. The purpose of this research article is to identify those specific major and minor ingredients contained in the Pfizer Vaccine, the Moderna Vaccine, the Astrazeneca Vaccine and theJanssen Vaccine using various scientific anatomical, physiological and functional testing for each SARS-COV-2-19 vaccine. As a human right, governed under World Law by the Nuremberg Code of 1947, the vaccine specific ingredient information is critical, required and necessary to know so that any human from any country in the World can make an informed decision whether or not to consent to the SAR-CoV-2-19 inoculation. We have conducted the scientific testing on each vaccine and have identified several ingredients or adjuvants that have not been disclosed which are contained in hese four SARS-CoV – 2 -19 vaccines. Currently, these vaccines are being administered to millions of humans around the World under an Emergency Use Authorization (EUA) issued by each country without full disclosure of all ingredients and in some cases mandated by governments or employers in violation of individual human rights under the Nuremberg Code of 1947.

Bharat Biotech chairman and MD Krishna Ella (right) and Serum Institute CEO Adar Poonawalla. Photos: Twitter and PTI. For all the Narendra Modi government’s desire to push an Indian company to the forefront of the national COVID-19 response, it has actually put an Indian company in an awkward, even untenable, position.

A Portuguese health worker has died two days after getting the Pfizer coronavirus vaccine. Sonia Acevedo, 41, suffered a ‘sudden death’ at home on New Year’s Day 48 hours after receiving the jab. An autopsy is expected to take place later today or tomorrow.

People affected by the 1984 Bhopal gas tragedy are being violated as trails of indigenous vaccine Covaxin–developed by Bharath Biotech–are being conducted on them without their consent, an activist claimed. The vaccine candidate is in its Phase-3 trial at the 

Aims of the study: Patient comprehension is a critical part of meeting medical ethics standards of informed consent in study designs. The aim of the study was to determine if sufficient literature exists to require clinicians to disclose the specific risk that COVID-19 vaccines could worsen disease upon

Public asks why only 516 people have been vaccinated – compared to a million-odd in the UK and 240,000 in Germany.

Vaccine manufacturers need to have protection against all lawsuits for their vaccines especially during a pandemic, Serum Institute of India (SII) Chief Executive Officer Adar Poonawalla has said. He also said that the vaccine makers are going to propose this to the government, while speaking at a virtual panel on the challenges of developing a Covid-19