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.
Our experienced attorneys have spent decades in the courtroom fighting the good fight for our clients. We have fought for years, litigating complex cases involving defective pharmaceuticals and medical devices, environmental contamination, product liability, toxic torts, and consumer fraud claims.
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Chris Coffin’s spent decades in the healthcare field and understands the difficulties any health complication brings. He’s here to help you navigate the process while fighting your own health battle.
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