Merck has been accused of committing fraud in its Gardasil vaccine safety trials putting millions of young girls at risk for ovarian failure or even death.
Gardasil is said to protect against cervical cancer, a disease that in the U.S., has a relatively low mortality rate of 1 in 43,478 (2.3 per 100,000)
In “The Plaintiff’s Science Day Presentation on Gardasil,” Robert F. Kennedy, Jr. reveals Merck data showing Gardasil increases the overall risk of death by 370%, risk of autoimmune disease by 2.3% and risk of a serious medical condition by 50%
Postmarketing and adverse events reported during use of the vaccine post-licensing are listed on the Gardasil vaccine insert and include blood and lymphatic system disorders, pulmonary embolus, pancreatitis, autoimmune diseases, anaphylactic reactions, musculoskeletal and connective tissue disorders, nervous system disorders and more
Merck’s use of a neurotoxic aluminum adjuvant instead of a proper placebo in its safety trials effectively renders its safety testing null and void, as the true extent of harm cannot be accurately ascertained
The HPV vaccine Gardasil was granted European license in February 2006,1 followed by U.S. Food and Drug Administration (FDA) approval that same year in June.2 Gardasil was controversial in the U.S. from the beginning, with vaccine safety activists questioning the quality of the clinical trials used to fast track the vaccine to licensure.3
Lauded as a silver bullet against cervical cancer, there have been multiple continuing reports since it was licensed that Gardasil vaccine has wrought havoc on the lives of young girls (and young boys) in the U.S. and in countries across the world. Serious adverse reactions reported to the Vaccine Adverse Event Reporting System (VAERS) in relation to Gardasil include but are not limited to:4
Anaphylaxis
Guillain-Barre Syndrome
Transverse myelitis (inflammation of the spinal cord)
Pancreatitis
Venous thromboembolic events (blood clots)
Autoimmune initiated motor neuron disease (a neurodegenerative disease that causes rapidly progressive muscle weakness)
Multiple sclerosis
Sudden death
Postmarketing experiences and adverse events reported during post-approval use listed on the Gardasil vaccine insert5 include blood and lymphatic system disorders such as autoimmune hemolytic anemia, idiopathic thrombocytopenic purpura and lymphadenopathy; pulmonary embolus; pancreatitis; autoimmune diseases; anaphylactic reactions; arthralgia and myalgia (musculoskeletal and connective tissue disorders); nervous system disorders such as acute disseminated encephalomyelitis, Guillain-Barre syndrome, motor neuron disease, paralysis, seizures and transverse myelitis; and deep venous thrombosis, a vascular disorder.
More
https://www.investmentwatchblog.com/merck-has-been-accused-of-committing-fraud-in-its-gardasil-vaccine-safety-trials-putting-millions-of-young-girls-at-risk-for-ovarian-failure-or-even-death/