Why did Prasad, Makary of FDA, NIH, HHS, CDC et al., for they really are ONE entity, approve Merck’s ENFLONSIA™ (clesrovimab-cfor) for Prevention of Respiratory Syncytial Virus (RSV) Lower Respiratory

Are we being fed BS constantly, just word games when NOTHING will change? Is the game really to make mRNA part of our daily lives in Trump 2.0 and these people who hold these positions now in our health agencies, their job is to bullshit us into silence and compliance, and make that happen while we think they are there to clean things up and fix things? When will they do opposite? I do not know. What is your view? I do not play with words, I see the FDA and NIH and CDC etc. as the same under Trump and Biden, no change. Just frills. And camera.

mRNA vaccine still remains. Deadly as it is with more expansion planned (self replicating, self-amplifying mRNA) and one of the inventors of the mRNA technology is on the ACIP committee. Is this the Twilight zone?

Reports are that the Merck vaccine Enfanzia or clesrovimab or ENFLONSIA (all 3 names are the same) a long-acting monoclonal antibody (mAb) has a near 12% severe adverse reaction profile. Did FDA know this? Will the new IMO compromised ACIP approve this?

Why were there 50% more deaths in the clesrovimab group over placebo and what are the 11.5% serious adverse events in clesrovimab vaccine arm? see charts below.

‘ENFLONSIA is a preventive monoclonal antibody designed to protect infants against a spectrum of RSV disease severity, including worsening disease requiring hospitalization

ENFLONSIA is the first and only RSV preventive option administered to infants using the same dose regardless of weight

RAHWAY, N.J.–(BUSINESS WIRE)– Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced the U.S. Food and Drug Administration (FDA) has approved ENFLONSIA™ (clesrovimab-cfor) for the prevention of respiratory syncytial virus (RSV) lower respiratory tract disease in neonates (newborns) and infants who are born during or entering their first RSV season. ENFLONSIA is a preventive, long-acting monoclonal antibody (mAb) designed to provide direct, rapid and durable protection through 5 months, a typical RSV season, with the same 105 mg dose regardless of weight. A typical RSV season usually spans autumn to spring of the next year.’

Merck said:

• ‘ENFLONSIA demonstrated a reduction in incidence of RSV-associated medically attended lower respiratory infections (MALRI) requiring ≥1 indicator of lower respiratory infection (LRI) or severity compared to placebo through 5 months (primary endpoint) by 60.5% (95% CI: 44.2, 72.0, p<0.001) (incidence rates: ENFLONSIA, 0.026; placebo, 0.065).

• ENFLONSIA demonstrated a reduction in RSV-associated hospitalizations through 5 months (key secondary endpoint) by 84.3% (95% CI: 66.7, 92.6, p<0.001) (incidence rates: ENFLONSIA, 0.004; placebo, 0.024), showing increasing efficacy with increasing disease severity.’

See ClinicalTrials.gov:

Study Results | Efficacy and Safety of Clesrovimab (MK-1654) in Infants (MK-1654-004) | ClinicalTrials.gov

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