#333 - Safe and Effective? Cheryl Grainger on mRNA, Regulators, and Real Risks

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About this guest -

Cheryl Grainger is a former self employed pharmaceutical training consultant turned independent researcher and public health advocate. With a deep understanding of the inner workings of the pharma world, she now dedicates her time to exposing regulatory failures, data manipulation, and the erosion of public trust in institutions like the MHRA.

After four years of persistence, Cheryl successfully forced the MHRA to release its Yellow Card Vaccine Monitor Pre-print, a dataset that should have been made public long ago. Her detailed analysis, published in two parts on her new Substack, uncovers the extent of the misinformation and statistical distortion surrounding COVID-19 vaccine safety claims, especially regarding serious adverse events and pregnant or breastfeeding patients.

Cheryl highlights how the MHRA has buried safety signals, ignored first-hand reports from vaccine recipients, and misrepresented the risk–benefit ratio from the earliest days of the rollout. Her work calls into question the entire premise of pharmacovigilance as it’s currently practiced by regulatory bodies captured by industry influence.

Through her writing and advocacy, Cheryl is shining a light on the systemic failures of the UK’s drug regulator and calling for maximum exposure of what she describes as continued obfuscation of critical safety data.

You can read her in-depth findings here:🔗 Part 1 – Misinformation Monitor🔗 Part 2 – Misinformation Monitor

If you value truth, transparency, and accountability in medicine, Cheryl’s work is essential reading. Please subscribe to her Substack, link below.

About this episode -

In this episode, I speak with Cheryl, who brings insider experience from the pharmaceutical world and a deeply analytical mind to everything that’s unfolded over the past few years.

We dive into the role of the MHRA, the UK’s drug regulator, and explore whether it’s truly serving public health or merely rubber-stamping products handed to it by pharmaceutical companies. Cheryl shares her concerns about the lack of transparency, the failures of pharmacovigilance, and how freedom of information requests have revealed troubling gaps in regulatory oversight, especially in relation to the COVID-19 vaccine rollout.

We talk about mRNA technology, gene therapy, and the disturbing trend of pushing products to market without adequate long-term safety data. Cheryl also highlights the yellow card system, supposedly in place to track adverse effects, which is shockingly underused