CBS/AP/ November 14, 2012, 12:40 PM

Pharmacy head pleads Fifth at meningitis outbreak hearing

Updated 5:10 p.m. ET

WASHINGTON Barry Cadden, the owner and director of the specialty pharmacy tied to a deadly fungal meningitis outbreak, declined to testify Wednesday morning before a congressional committee investigating the matter.

Cadden, co-founder of the New England Compound Center, told lawmakers he would use his Fifth Amendment right to not answer questions in order to avoid self-incrimination.

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After repeated questioning by House lawmakers, Cadden told the House Energy and Commerce Committee: "Under advice of counsel, I respectfully decline to answer under basis of my constitutional rights and privileges, including the Fifth Amendment."

Lawmakers continued to ask Cadden questions about the contamination of steroids used to treat patients -- many for back pain -- that has sickened nearly 430 people with fungal meningitis and caused 32 deaths. Another 10 patients have peripheral joint infections from injections.

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A recent investigation of the NECC facility in Framingham, Mass., found numerous sterility issues, including bacterial contamination and mold growth in areas where drugs are prepared. Compounded drugs are supposed to be prepared in temperature-controlled clean rooms to maintain sterility.

The NECC has been closed since early last month, and Massachusetts officials have taken steps to permanently revoke its license. The pharmacy has recalled all the products it makes, including about 17,700 single-dose vials of a steroid that up to 14,000 patients my have received.

Fungal meningitis causes inflammation of the lining of the brain and spinal cord.

Republicans lawmakers, who make up the majority of the House, focused on NECC's history of troubles, when questioning why regulators at the Food and Drug Administration and the Massachusetts board of pharmacy did not take action against the pharmacy years earlier.

"After a tragedy like this, the first question we all ask is: could this have been prevented?" asked Rep. Cliff Stearns, R-Fla. "After an examination of the documents provided by the Massachusetts Board of Pharmacy and the FDA - the answer here appears to be yes.

A timeline assembled by the Republican staff shows that the FDA inspected NECC three times since 2002 for sterility issues. The Massachusetts board of pharmacy investigated at least 12 separate complaints involving the pharmacy, dating back to its founding.

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"I was stunned and angered to learn that an inspection of the NECC by the FDA and the Mass Board over 10 years ago identified contamination in the very same drug at issue in the current outbreak," said Rep. Fred Upton, R-Mich., who chairs the Energy and Commerce committee.

FDA Commissioner Margaret Hamburg told lawmakers that the problems uncovered in inspections were "very serious," but that the agency was obligated to defer to Massachusetts authorities, who have more direct oversight over pharmacies.

"The challenge we have today is that there is a patchwork of legal authorities that oversee the action we can take," said Hamburg, who was nominated to head the FDA by President Obama in 2009.

Hamburg asked lawmakers Wednesday in prepared testimony to give her agency more authority and funding to oversee compounding pharmacies.

"In light of growing evidence of threats to the public health, the administration urges Congress to strengthen standards for non-traditional compounding," Hamburg told lawmakers.

Compounding pharmacies traditionally fill special orders placed by doctors for individual patients, turning out a small number of customized formulas each week. They are typically overseen by state pharmacy boards, though the Food and Drug Administration occasionally steps in when major problems arise. Some pharmacies have grown into much larger businesses in the last 20 years, supplying bulk orders of medicines to hospitals that need a steady supply of drugs on hand.

She said Congress should put in place a two-tier system in which traditional compounding pharmacies continue to be regulated at the state level, but larger pharmacies would be subject to FDA oversight.

Cadden's appearance before the committee came immediately after the widow of a longtime Kentucky judge who was the first confirmed victim of the outbreak.

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Speaking without notes, Joyce Lovelace told lawmakers her story of more than 50 years of marriage to 78-year-old Eddie C. Lovelace, who was a circuit judge until he died Sept. 17 at Vanderbilt University Medical Center.

She asked lawmakers to implement laws to police companies like the New England Compounding Center, which distributed steroids that tested positive for contamination.

"My family is bitter, we are angry, we are heartbroken and devastated. I come here begging you to do something about the matter."

CBS Evening News correspondent Jim Axelrod reported on Tuesday that Rep. Stearns had expected Cadden to take the Fifth and stay silent.

One incident he was hoping to get answers on occurred in September 2004, when FDA investigators asked Cadden if he had "Trypan Blue" solution on hand. The product is not approved by the FDA.

The CBS News investigative team's Laura Strickler reports that investigators then found a drawer labeled Tryban Blue that contained 189 vials of the drug. When presented with their findings, Cadden reportedly became "indignant" and told the company's co-owner Greg Conigliaro to no longer answer the investigators' questions.

Another company owned by Cadden and Conigliaro, Ameridose, was also discovered to have sterility issues during a recent inspection when investigators found insects and birds inside the facility. The company will be shut down until Nov. 19 at the earliest, and has had to lay off 650 employees and an additional 140 employees at its marketing and support arm because of the extended closure.

© 2012 CBS Interactive Inc. All Rights Reserved. This material may not be published, broadcast, rewritten, or redistributed. The Associated Press contributed to this report.
15 Comments Add a Comment
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MIO42 says:
Humbug plays a huge role in this also
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MIO42 says:
Sounds like HUMBUG won't own this one!

Curious?
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ttipbc says:
So he takes the 5th? Times like this are when we need an agency like Massod to kidnap & torture this SOB until he does confess, then (literally) give him a dose of his own medicine.
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Swift29 says:
Just re: the headline: How convenient.
Any wonder that we need the FDA and other gov agencies to protect us from crooks. This is the truth, there was a company selling baby food full of broken glass, I kid you not, and the execs were found guilty. This is what deregulation has brought us to. "No let the invisible hand make everything alright.' 'Let everyone look out for number one.' Yeah.....
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lralperstein says:
In view of the gross negligence on the part, not only of NECC staff but also on the part of government regulators, criminal charges should be brought against all those individuals, including those in the government, who contributed to the meningitis outbreak. Its obvious that government regulators turned a blind eye to the most elementary practice of sterility in their monitoring of these companies, and thus protecting the public, that it could be said in so doing that they intentionally caused this meningitis outbreak. In addition, the fact that so much time has past since the outbreak began without definitive action being taken, it's obvious that the government is continuing to turn a blind eye and in so doing protect all those individuals involved. This is an obvious case of gross negligence not only on the part of the NECC but also of government regulators. The time is now to file criminal complaints against all involved. Whose pockets were lined to close a blind eye? I would check the bank accounts of of those government employees who were paid TO DO NOTHING.
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tomanyt replies:
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@LRALPERSTEIN...LOL
THALES457 replies:
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LET US TAKE THIS OCCASION TO REFLECT ON THE FACT THAT THE REPUBLICANS HAVE BEEN AGITATING FOR FEWER REGULATIONS. OKAY MITT, WHERE DO WE CUT FIRST? THEY ARE THE PAID SERVANTS OF THE RICH AND SEEK TO FOOL THE WORKINGMAN. THEY WILL MAKE MUCH OF BENGHAZI WHERE FOUR DIED AND MAKE LITTLE OF THESE MALEFACTORS OF GREAT WEALTH WHO HAVE 8 TIMES AS MANY ON THEIR CONSCIENCE. CONSCIENCE. WHAT AM I THINKING?
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Sabby2174 says:
Inject him with the contaminated injections instead of lethal injection on his deathbed. Vendetta, we need you!
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WitchBroom says:
Sentence the guy by having to hand dig and backfill graves for the next year, then on his last day give him an injection of his medicine.
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nohater says:
too bad he can't be executed for his crimes. people are dead and he takes the 5th. if it were my call, he would be executed. fortunately for him, it's not my call.
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THALES457 says:
JUST A GUESS = THE PROBLEM WAS NO CLEANROOM OF THE TYPE USED FOR PARENTERALS (GRADE A OR GRADE B). FDA REQUIRES BIG PHARMA TO BUILD THESE. FDA DOES NOT REGULATE SMALL FOLKS. SMALL FOLKS I AM GUESSING USED SMALL LOCALIZED ENVIRONMENTS CALLED MANY NAMES: BIOLOGICAL SAFETY CABINETS, LAMINAR FLOW WORK STATIONS, SASH HOODS, ETC. THESE DO NOT HAVE THE "CLEAN-A-BILITY" OF THE MUCH LARGER LAMINAR FLOW GRADE A OR B CLEANROOMS. THEN THERE IS ALSO THE PROBLEM OF THE AIR HANDLERS WHICH SERVE AS RESERVOIR, AMPLIFIER AND DISSEMINATOR AND ARE VERY TRICKY FOR FUNGI AND BACTERIA. A SMALL ROOM USING SASH HOODS TO PROVIDE THE ENVIRONMENT WILL BE SERVED BY AIR HANDLERS. THE ZONE OF NEGATIVE PRESSURE AROUND THE SASH (BERNOULI'S EFFECT) WILL INDUCE AHU SUPPLY AIR INTO THE ENVIRONMENT. CBS CALL JACOBS ENGINEERING IN CONSHOHOCKEN OR SIMILAR ENGINEERING FIRM. I HAVE NO AFFILIATION WITH THEM. KEEPING FUNGI OUT IS AN ELABORATE AND EXPENSIVE DESIGN PROJECT. IF THE FDA IS NOT THERE DEMANDING THAT MONIES BE SPENT, THEY WILL BE KEPT AS PROFIT. YOU NEED A COP ON THE STREET CORNER. INJECTABLES AND PILLS HAVE VERY DIFFERENT MANUFACTURING REQUIREMENTS.
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GossamerWings says:
Throw him in jail for 30 years.
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KodeBloo replies:
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That's not even a year for each death he's responsible for. What about the people who survived?
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