The risk of COVID vs the risk of vaccine side-effects

[Majulah]

Parmaceuticals is one of the most heavily regulated industries in the world. Vaccine development, production and supply normally follows a long process of study and oversight from both private and public bodies. This generally lasts at least 10 years but laws are in place that allow the process to be cut short in times of national emergency. According to a research article published on PLOS ONE, “the average vaccine, taken from the preclinical phase, requires a development timeline of 10.71 years and has a market entry probability of 6%.”

The UK government approved the supply of the COVID-19 vaccines through temporary authorisation laid out by the Human Medicine Regulations of 2012. The 2012 Regulations were updated on 16 October 2020 to cover:

• temporary authorisations for the COVID-19 vaccines;
• civil liability and immunity for those taking part in the vaccination programmes;
• expanding the healthcare workers who can administer vaccines;
• vaccine promotion;
• an exemption to wholesale licensing requirement.

Vaccine candidates worldwide including AstraZeneca, Johnson & Johnson, Moderna, Pfizer/BioNTech, Sinovac and Sputnik have been given emergency use authorization. Authorization was fast-tracked because of the declared emergency.

Anyone taking the vaccines are therefore part of a clinical trial. The AstraZeneca Phase 3 trial ends in 2023, Moderna Phase 3 trial ends in 2022 and the Pfizer Phase 1/2/3 trial ends in 2023. As of April 2021, the Johnson & Johnson the single-shot vaccine was in the Phase IIa trial.

Despite heavy regulation, the pharmaceutical industry has repeatedly been involved in civil and criminal violations resulting in
heavy damage payments. Pfizer’s settlement for $2.3 billion in 2009 was the largest case of pharmaceutical and health care
fraud in US history. AstraZeneca and Johnson & Johnson are also listed among the largest pharmaceutical settlements reached
in the US for fraud, off-label promotion and kickbacks.

The media reports that the new COVID-19 vaccines are safe. Nevertheless, in 2020, the British government gave AstraZeneca and Pfizer protection from liability of any damages resulting from their use.

The risk of COVID vs the risk of vaccine side-effects​

COVID-19 risk​

To assess the risk of the vaccines we first need to ask what are the risks of COVID-19? This has already been established by experts worldwide, such as Professor John Ioannidis of Stanford University.

In at least 80% of cases, the virus produces either no symptoms or a mild cold-like illness. The infection fatality rate for COVID-19 is 0.15%-0.2%. This brings it close to seasonal flu which is around 0.1%-0.2%.

• Children have a greater chance of being struck by lightning than dying of COVID-19.
• Adults are more likely to die in a car accident.

Most of the population have no risk of dying from COVID-19. Studies show that 99.94% survive COVID-19 and will be resistant for a long time. The QCovid risk calculator from Oxford University can be used to calculate your risk of death or hospitalisation.

Vaccine safety​

COVID vaccination safety and the risk of adverse drug reactions (ADRs) have yet to be fully studied as they are currently undergoing clinical trials. Vaccine development generally takes 10-15 years and the current vaccines have been released under emergency use authorization only. Vaccine manufacturers AstraZeneca and Pfizer have granted protection from future product liability claims.

See below for emerging evidence of side-effects from the current vaccine rollout.

People in the UK are coming forward to tell of life-changing side-effects after receiving the jab. You can listen to their stories here.

GOTO
https://evidencenotfear.com/covid-19-vaccination/
where u can click on links [ emerging evidence ] , [ tell of life-changing side-effects ].