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🕵️♂️ Revealing the Hidden Side of the FDA: Uncovering Unseen Realities!
Join us in this eye-opening video as we shed light on the lesser-known aspects of the FDA (Food and Drug Administration).
🚀 Delve into the untold story behind the FDA as we discuss:
- The original intent and function of the FDA.
- Instances of regulatory shortcomings and the consequences for public health.
- Notable cases involving conflicts of interest and compromised safety.
- The delicate balance between ensuring consumer safety and supporting pharmaceutical innovation.
🎯 This video is for:
- Those concerned about the integrity of regulatory agencies.
- Individuals seeking a comprehensive understanding of FDA's challenges.
- Advocates of transparency and accountability in the pharmaceutical industry.
🤯other examples of the darkside of the FDA
-Thalidomide Tragedy (1960s): The FDA was criticized for its slow response to the thalidomide crisis. Thalidomide, a drug used to alleviate morning sickness in pregnant women, led to severe birth defects. While the drug was not approved in the US, the FDA's perceived lack of vigilance raised concerns about its ability to prevent dangerous drugs from entering the market.
-Vioxx Recall (2004): The painkiller Vioxx was withdrawn from the market after it was linked to an increased risk of heart attacks and strokes. Critics argued that the FDA had not acted swiftly enough to address safety concerns, leading to thousands of adverse events.
-Opioid Epidemic: The FDA faced criticism for its role in the opioid epidemic. It approved powerful painkillers like OxyContin and did not adequately address concerns about their potential for abuse and addiction. Critics argue that the FDA's approval processes contributed to the widespread over prescription of these drugs.
-Fast-Tracking of Drugs: The FDA's expedited approval processes, like the Accelerated Approval Program, have come under scrutiny for potentially allowing drugs onto the market without sufficient long-term safety data. This can lead to unforeseen adverse effects emerging after the drugs are widely used.
-Conflict of Interest: The FDA has faced allegations of conflicts of interest, with some officials having ties to the industries they regulate. Critics argue that this can influence decision-making and weaken the agency's ability to hold companies accountable for safety concerns.
-Lack of Regulation for Supplements: The FDA's regulation of dietary supplements has been criticized for being less stringent compared to its regulation of pharmaceuticals. This has allowed some questionable products to enter the market without thorough safety and efficacy evaluations.
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🎉 Join the conversation! Share your thoughts on the regulatory landscape and the balance between consumer safety and industry interests in the comments below. Let's work towards a more transparent future.
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We're two Puerto Ricans from New York City that just talks about whatever we want, from Politics to religion.
Almost nothing is off-limits and we have an opinion on everything. If you are looking for fact-based reporting, you are in the wrong place but if you want a heavy opinion, welcome, we want to hear yours too.
#FDADarkSide #RegulatoryChallenges #PharmaceuticalIndustry
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