…Contains Ingredients Linked to Aborted Fetuses (Read Package Insert)
The Centers for Disease Control and Prevention (CDC) issued a health alert advisory after a case of measles was confirmed in Kentucky, Reuters reported on Friday. The agency “asked physicians to recommend measles, mumps and rubella shots for patients who are unvaccinated or not fully vaccinated,” according to the report.
But has the new MMR vaccine been tested for cancer risk, toxicity, or fertility problems? What ingredients does the vaccine contain? What potential adverse reactions have been identified? Is there long-term safety data? Does the vaccine contain living viruses? And are vaccinated individuals able to transmit the virus to others?
NEW MMR VACCINE “PRIORIX” NOT TESTED FOR CANCER RISK, TOXICITY OR FERTILITY PROBLEMS, ACCORDING TO PACKAGE INSERT:
The new measles, mumps, and rubella (MMR) vaccine, called “Priorix” by GlaxoSmithKline, which was only approved by the U.S. Food and Drug Administration (FDA) in June of last year, has not been tested for toxicity risk or fertility problems.
“PRIORIX has not been evaluated for carcinogenic or mutagenic potential or for impairment of
fertility,” the package insert for the pharmaceutical drug reads.
Carcinogenesis is the process by which normal cells transform into cancer cells due to genetic and environmental factors. There is no information available about whether Priorix has the ability to cause cancer.
Mutagenesis refers to the process by which genetic material (DNA) is altered or mutated, potentially leading to genetic disorders or cancer. There is no information available about whether Priorix has the ability to cause genetic mutations.
The statement that Priorix has not been evaluated for impairment of fertility means that there is no evidence or information available about whether the vaccine has the potential to negatively affect reproductive function or fertility in men or women.
PRIORIX VACCINE CONTAINS INGREDIENTS LINKED TO ABORTED HUMAN FETUSES:
Moreover, one of the ingredients in the Priorix vaccine can be linked to aborted human fetuses.
The vaccine insert says that the drug was created using the “Wistar RA 27/3 strain of live attenuated rubella virus,” which “is propagated in MRC-5 human diploid cells.”
MRC-5 human diploid cells are derived from the lung tissue of a fetus that was aborted in the 1960s.
ADVERSE REACTIONS TO PRIORIX VACCINE INCLUDE BLOOD AND IMMUNE SYSTEM DISORDERS, NERVOUS SYSTEM DISORDERS, AND INFECTIONS:
The following adverse reactions have been identified after vaccination with Priorix, according to the package insert:
- Blood and lymphatic system disorders such as thrombocytopenia, thrombocytopenic purpura
- Vascular disorders such as vasculitis (including Henoch-Schönlein purpura and Kawasaki syndrome)
- Immune system disorders such as anaphylactic reactions
- Infections and infestations such as meningitis, measles-like illness, mumps-like illness (including orchitis, epididymitis, and parotitis)
- Musculoskeletal and connective tissue disorders such as arthralgia and arthritis
- Nervous system disorders such as encephalitis, cerebellitis, cerebellitis-like symptoms (including transient gait disturbance and transient ataxia), Guillain-Barré syndrome, transverse myelitis, peripheral neuritis and afebrile, seizures, and syncope
- Skin and subcutaneous tissue disorders such as erythema multiforme
“Not everybody who receives a shot will suffer all of these adverse events. But for the people who suffer one of these events, like encephalitis, it has changed their life and their family’s lives forever,” said Dr. Richard Bartlett, a 30-year Texas physician and former advisor to then-Texas Governor Rick Perry’s Health Disparities Task Force.
“We’ve learned many lessons as a result of receiving the Pfizer data from the FDA as the result of a FOIA (Freedom of Information Act) request,” he added. “Firstly, although the FDA and the pharmaceutical company were aware of over 1,200 adverse events related to their product, did they chose not to be transparent nor to voluntarily share the information with the public or the medical community without extreme pressure, including a FOIA request and a hearing in federal court in Fort Worth, Texas?”
“Can we count on pharmaceutical companies to share information about safety and adverse events related to their products without a FOIA request and a federal case?” asked Dr. Bartlett, recipient of the Meritorious Service Award from Texas’ Health and Human Services (HHS).
ADVERSE EVENTS ONLY TRACKED FOR LIMITED TIME FOLLOWING PRIORIX VACCINATION, LONGER-TERM EFFECTS NOT INCLUDED IN AVAILABLE DATA:
According to the package insert for Priorix, unsolicited adverse events that occurred within 43 days following vaccination were recorded using diary cards supplemented by medical review.
Data on solicited adverse reactions and unsolicited adverse events were transcribed into the study database during an on-site visit on Day 42 and via telephone contact on Day 180.
It is important to note that adverse events were only tracked for 180 days following vaccination, meaning there is no longer-term safety data.
PRIORIX CONTAINS LIVE VIRUSES:
Priorix contains “live attenuated measles, mumps, and rubella viruses,” according to the package insert, meaning that the viruses in the vaccine are weakened but alive.
VACCINATED INDIVIDUALS COULD SPREAD THE VIRUS & INFECT OTHERS:
Under the section titled “Risk of Vaccine Virus Transmission,” the Priorix insert says that “Live attenuated rubella vaccine virus has been detected in the nose and throat of individuals up to 28 days after vaccination with a rubella virus-containing vaccine.”
This means that individuals who have recently received the vaccine could shed the virus in their nasal and throat secretions, spreading the virus to others and possibly infecting them.
“Are people who have cancer or who are on immunosuppressive medicine because they’ve had organ transplants at risk for potential death or disability if they become infected with these lab-manipulated live, contagious viruses,” says Dr. Bartlett.
Bartlett discovered a safe and effective treatment for all early and late symptoms of COVID-19 using budesonide, an inhaled steroid that could have prevented 90% of hospitalizations. That discovery was later corroborated by Oxford University.
“Have we seen that lab-manipulated, live, contagious viruses lead to disaster? Case in point, there appear to be more new polio cases in Africa resulting from lab-manipulated, live polio vaccines than the natural wild polio strain. Reports show Angola, Benin, Cameroon, Central African Republic, Chad, Côte d’Ivoire, Democratic Republic of the Congo, Ethiopia, Ghana, Nigeria, Togo, and Zambia have experienced outbreaks of vaccine-derived poliovirus,” the doctor went on to say.
READ THE PRIORIX PACKAGE INSERT BELOW: