In 2006, the Gardasil vaccine by Merck & Co. debuted. Approved by the U.S. Food and Drug Administration (FDA) for use in preventing infection from just a handful of the hundreds of types of human papillomavirus (HPV) strains. Since the Gardasil vaccine debuted, thousands of adults and adolescents have reported severe side effects of the vaccine – the most common being postural orthostatic tachycardia syndrome (POTS).
How Did This Happen?
The FDA approved Gardasil in just six months, a process that was clearly too fast to ensure efficacy and safety. And now, thousands of young men and women suffer severe reactions to the vaccine after having trusted that it and its manufacturer did the due diligence to ensure a healthy and safe product.
They didn’t, and now thousands of people are left impacted. It’s not right and needs to be rectified going forward, and Merck & Co. needs to make restitution to those parties harmed.
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