FDA Delays Our H1N1 Vaccine Petition… What Pandemic Emergency?

By Administrator on February 18, 2010 No Comments

Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org

Is H1N1 “Swine Flu” a “novel” virus that has caused a “pandemic” — or is FDA too busy with other matters to address what President Obama declared to be a National Health Emergency on October 24, 2009? Just what do the bureaucrats at FDA actually think they’re doing?

Updates: http://drrimatruthreports.com/?p=3429

You know about our “Stop the Shot” Lawsuit intended to challenge the FDA’s approvals of the alleged “novel” H1N1 flu virus vaccine as what FDA claims to be a mere “change of strain” vaccine not requiring safety testing… For an update on the status of the refiling of that suit see: http://drrimatruthreports.com/?p=4708. But the suit is not our only “Push Back” regarding the fake “Swine Flu” pandemic. Prior to filing the lawsuit in October, we had filed a Citizens Petition on August 31, 2009, complaining to the FDA about the Federal government’s irrational response to the alleged “Swine Flu” pandemic. See: http://drrimatruthreports.com/?p=3429.

So what is the FDA doing about the “National Health Emergency” over the Pandemic that was declared last April? Well, not much. After your PUSH BACK stopped the plan to force everyone in the US to receive dangerously untested and adjuvanted vaccines, FDA has been rather quiet… well, other than announcing a few weeks ago that a “Third Wave” of the “pandemic” is on the way. And, apparently allowing the H1N1 vaccine to be admixed with the Seasonal Flu vaccine. See: http://www.kgmi.com/pages/6391069.php?contentType=4&contentId=5605584.

So what does FDA want to do about our Citizens Petition? Uh, Uhm… nothing. Why? Because there are sooo many more “important” things for FDA to deal with than an alleged National Health Emergency. I kid you not. I suppose the FDA needs to focus on approving prescription drugs for, say, toenail fungus. Well, after all, half of all the drugs FDA approves are either taken off the market as too dangerous or have their indications severely limited. I reproduce the FDA letter below.

Ralph Fucetola JD
Natural Solutions Foundation
Trustee and Counsel

Letter from FDA

FDA Delay Letter