Mobile UPI  |   About UPI  |   UPI en Español  |   UPI Arabic  |   UPIU  |   My Account
Search:
Go

Hearings to be held on anthrax vaccine

|
|
 
  
Published: March. 11, 2005 at 10:23 PM
By DEE ANN DIVIS, Senior Science & Technology Editor
Advertisement

WASHINGTON, March 11 (UPI) -- Congress will look into whether the Department of Health and Human Services overstepped its authority when it gave the Department of Defense permission to vaccinate military personnel with a controversial anthrax vaccine despite a court injunction halting the program.

The hearings will be called in the next couple of months by Rep. Christopher Shays, R-Conn., chairman of the House Subcommittee on National Security, Emerging Threats and International Relations. Shays has been asking HHS officials for information on their decision to approve the Emergency Use Authorization since it was issued Jan. 14 at the request of the Defense Department.

HHS made its ruling based on the new Bioshield Act, which grants the Secretary of Health and Human Services the right to permit use of a vaccine for an otherwise-unapproved use if there is an emergency or potential emergency.

Paul Wolfowitz, the deputy secretary of defense, asked for permission in a Dec. 10 letter saying he had "determined there is a significant potential for a military emergency involving a heightened risk to the United States military forces of an attack with anthrax."

That use of Bioshield is beyond the intention of Congress, Shays said.

"We believe HHS acquiescence in the DoD request unjustifiably expands and distorts the scope of emergency use authority envisioned by the Act and strays well beyond the legislative intent of the provision," Shays wrote in a March 9 letter to HHS Secretary Michael Leavitt.

The anthrax vaccine, called Anthrax Vaccine Absorbed or AVA, manufactured by Bioport of Lansing, Mich., has been the subject of three lawsuits, a congressional investigation and some 100 courts-martial of personnel refusing the vaccination. Critics of the program say the medication can cause serious, even life-threatening, reactions and is not approved for the prevention of inhalation anthrax -- the biodefense application at the center of the DOD vaccination program.

DoD and Bioport assert the vaccine is safe, pointing to 18 studies, including one by the Institute of Medicine saying the vaccine is no more dangerous than any other vaccine.

Federal District Court Judge Emmet Sullivan agreed with critics and granted an injunction Oct. 27 against the mandatory program for a second time, pending new steps by the Food and Drug administration to finish the proper approval process and clear the vaccine for its specific use against inhalational anthrax.

Though it would still be possible to give soldiers the vaccine with their informed consent under the injunction, DoD sought an alteration of the injunction in light of the HHS ruling.

"When the Bioshield Act first passed the House, Mr. Shays was very concerned about a provision in the original bill that talked about waivers of certain informing requirements for emergencies in the military," said a congressional staff member speaking on condition of anonymity. "We put it in Title 10, some years before, that if you are going to use an (investigational drug) on U.S. forces, that has to be presidentially approved after a process where the secretaries of HHS and DoD say what it means and why they have to do it that way."

After some negotiation, the aide said, the House agreed that members of the military should be allowed to consent to receive either unapproved drugs or drugs that were licensed but used in an unapproved way.

"There was a colloquy on the floor between then chairman (Billy) Tauzin (R-La.) and Mr. Shays to the effect that the (Bioshield) provision was too broadly written."

Colloquies are a form of scripted conversation held during a congressional session as a way to enter discussion into the record and often are used to express congressional intent.

The Senate also acknowledged restrictions to waivers, even if the situation involved a new use for an already licensed product.

"You still need to inform those receiving the drug," said the aide.

A spokesman for HHS said the department was drafting response to both letters, but he would not comment on the letters or the possibility of a hearing.

--

E-mail: ddivis@upi.com

Topics: Christopher Shays, Emmet Sullivan, Michael Leavitt, Paul Wolfowitz
© 2005 United Press International, Inc. All Rights Reserved. Any reproduction, republication, redistribution and/or modification of any UPI content is expressly prohibited without UPI's prior written consent.

Order reprints
  
Join the conversation
Most Popular Collections
Notable deaths of 2012 Scripps National Spelling Bee AmfAR Cinema Against AIDS gala
Indianapolis 500 Presidential Medal of Freedom Memorial Day around the nation
Additional Science News Stories
1 of 32
Marilyn Monroe Cupcake Portrait at Madame Tussauds in New York
View Caption
A one-of-a-kind 8 x 4 foot portrait of Marilyn Monroe made from 2,100 bite sized stuffed cupcakes stands in the lobby next to her wax figure on the eve of Marilyn Monroe's 86th birthday at Madame Tussauds in New York City on May 31, 2012. UPI/John Angelillo
fark
Paralyzed rats. See how they run. They all ran after the scientist's wife, who cut their spines...
Murderer admits to eating victim's heart and brains, made no comment on the appropriate wine pairing...
According to FB, Drew is drunk as Cooter Brown and up to shenanigans. Grab yer popcorn
Photoshop this side dish
When stripper poles are outlawed, only outlaws will have stripper poles
Canada's secret space program announces its first incredible success