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BREAKING: Recommendations for MAHA & First Do No Pharm film features in mainstream US television today ๐ฅ Key points : MILLIONS of people have been killed by medical research fraud Big Pharma should no long longer be allowed to test their own drugs and control the data The FDA... show more
133,735 views โข 1 year ago โขvia X (Twitter)
9 Comments

Proud of you @DrAseemMalhotra Thank you .. #MAHA

Your Dad will be BEAMING with pride from above amazing man. Youโre a genuine force for good ๐๐ผ

@LadyLibertyinAZ They should NEVER have been able to test their own drugs. A five year old could tell you that.

And millions more will be ๐๐ป

Dr Malhotra, thank you sounding the alarm on statins. I listened to your podcast a couple of years ago on Joe Rogan. I refused them last year when my doctor tried to prescribe them. I had to refuse again a few months later when he sent the script to the pharmacy. Yes I have borderline high LDL and always have. I guess turning 60 was the big deal. Stress test normal, cardiac calcium in the normal range, need to improve my diet a bit. There is no way I will put a statin in my body. The side effects especially the pain are hard no for me. I am already a chronic pain patient with severe facet syndrome. Implanted a SCS almost 6 years ago to not be on pain medication. Thank you.

A prohibition on Big Pharma being allowed to test their own drugs would likely require Congressional action but here are a few alternative actions I believe the FDA could take. These could be the subject of citizen petitions to the FDA. Mandate Independent Audits of Clinical Trial Data: Require independent third-party audits of all clinical trial data submitted for drug and vaccine approvals to ensure accuracy and integrity. These audits would be conducted by FDA-approved entities unaffiliated with the sponsor. Public Access to Clinical Trial Data: Require full transparency by mandating the public release of all clinical trial protocols, raw data, and results submitted to the FDA, subject to privacy protections. This data should be made available on a publicly accessible database managed by the FDA or a designated third party. Strengthen Oversight of Data Analysis: Require that data analysis and interpretation for pivotal clinical trials be conducted by independent biostatisticians or FDA-appointed experts, in addition to sponsor analyses. The sponsorโs role in the analysis should be limited to collaboration rather than sole control. Enhance Conflict-of-Interest Disclosures: Expand requirements for disclosure of financial relationships between sponsors, researchers, and trial sites in all clinical trial documents submitted to the FDA. The FDA should make these disclosures publicly available. Incentivize Independent Trials: Establish a voluntary program encouraging sponsors to use independent contract research organizations (CROs) to conduct clinical trials, with expedited review for submissions that meet enhanced independence and transparency criteria.

@RobertKennedyJr @realDonaldTrump are you listening?

It SICKENS me to see YouTube content for kids interrupted with coercive ads for unnecessary and potentially harmful VACCINES!

The Australian TGA takes 97% of funding from Big Pharma. It is completely conflicted. It's totally WRONG!
