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The Medicines and Healthcare products Regulatory Agency (MHRA), which polices the safety of drugs used in the U.K., told MailOnline it is currently reviewing data on Moderna's vaccine.
The pharmaceutical firm has submitted evidence in the hope of getting its jab approved for children aged six months and older, as it is in the EU and U.S. Only over-fives can currently get Covid vaccines in the U.K.
Any approval of jabs for babies would cause huge controversy. British authorities have so far held out on approving jabs for infants despite massive pressure, due to concerns that the benefits do not outweigh any potential risks. Children rarely get seriously ill with Covid and the majority are thought to have already been infected.
Experts said today that, even if approved, the jab must not be rolled out "en masse" to healthy infants.
Dr. Laura Squire, the MHRA's Chief Healthcare Quality and Access Officer, revealed the regulator was processing an application from Moderna. But she added the mRNA jab, which works in a similar way to Pfizer's, would only be approved if it met strict safety and efficacy standards.
Note that there are 4 different contracts here dated 10 Dec 2020, 4 March 2021, 7 April 2021 and 28 Sept 2021. The documents show the number of doses ordered per month (but the price is redacted). But, note that even the latest of these contracts (dated 28 Sept 2021) contains the following statement in Article 1 (it's on page 17/25 of the scanned document)
"The ...State further acknowledges that the long-term effects and efficacy of the Vaccine are not currently known"
While that may have been a reasonable statement to include in the December 2020 contract, it is curious that no update at all had been added by the end of September 2021 given all the data on hundreds of millions of doses that had been adminstered by then.
Regarding the Pfizer contract with the UK (which presumably has the same wording) it is very interesting to note that this UK Government report ("Conditions of Authorisation for COVID-19 Vaccine Pfizer/BioNTech (Regulation 174", updated 16 Aug 2022) says:
"Pfizer/BioNTech must provide a regular analysis of safety data based on the MHRA's specifications relating to booster or supplementary doses"
I assume we are still waiting....
The fluoride products used in water fluoridation (sodium fluoride or fluorosilicic acid) are classified as hazardous waste products of the fertilizer, aluminum, and nuclear industries. They are even more toxic than naturally-occurring fluoride, since they contain other components, such as arsenic, lead, barium, and/or aluminum. See this.However, even naturally-occurring fluoride, in areas with high concentrations (over 1 ppm) has been found to have extremely adverse health effects. Even before additional fluoride is added, the level of natural fluoride in the water in many areas in the U.S. is already equal to the amount of naturally-occurring fluoride that has been found to cause skeletal fluorosis in other countries.
Comment: See also: