Thursday, June 04, 2015

NIH Statement On Discovery Of Contaminated In-House Meds










# 10,148


In a story reminiscent of 2012's Fungal Meningitis outbreak due to contaminated injectables produced by a compounding pharmacy (see MMWR: Multistate Outbreak Of Fungal Meningitis ), the NIH has announced an immediate halt to in-house compounding of injectable drugs after fungal contamination was found in several vials.
An investigation has turned up serious deficits in the in-house production of these drugs and operations have been suspended until they can be addressed. 

The good news is, the number of patients that may have been exposed to contaminated products is reportedly much lower than what we saw three years ago, and none of the recipients have shown any signs of infection.

The not-so-good news is this is simply the latest in a series of high profile lab incidents at government run institutions over the past 12 months, which has included the mishandling of Ebola, Anthrax (repeatedly), H5N1, and the discovery of a long forgotten vial of smallpox.


Here is the statement from the NIH.

For Immediate Release: Thursday, June 04, 2015 
NIH suspends operations in its Clinical Center Pharmaceutical Development Section

The National Institutes of Health (NIH) Clinical Center has suspended operations of its Pharmaceutical Development Section (PDS) due to the discovery of serious manufacturing problems and lack of compliance with standard operating procedures. Upon receipt of a complaint, Food and Drug Administration (FDA) representatives inspected the PDS between May 19 and May 29, and found a series of deficiencies that will require the NIH Clinical Center to take a number of corrective actions.

The facility makes products for certain clinical research studies conducted in the hospital and collaborating facilities. In April, two vials of albumin, used for the administration of the drug interleukin in experimental studies, were found to have fungal contamination. Vials made from the same batch were administered to six patients, although it is unknown whether those or other vials were contaminated. The six patients have been notified and are being followed closely for any signs of infection. At this time, none has developed signs of infection or illness. 
“This is a distressing and unacceptable situation,” said NIH Director Francis S. Collins, M.D., Ph.D. “The fact that patients may have been put in harm’s way because of a failure to follow standard operating procedures in the NIH Clinical Center’s Pharmaceutical Development Section is deeply troubling. I will personally oversee the steps to protect the safety of patients and remedy the situation as swiftly as possible.” 
Among the problems the FDA identified in their inspection were deficiencies in the physical facility, including flaws in the air handling system, and operational failures including inadequate quality control, insufficient employee training, and lack of compliance with standard operating procedures. Deficiencies of lesser significance were identified in the Clinical Center Pharmacy. The FDA inspection reports are available here: http://www.cc.nih.gov/phar/pdfs/483.pdf (PDF - 1.31KB)
The following steps are being taken immediately to protect patients:
  1. Operations of The Pharmaceutical Development Section have been suspended and no products will be made or distributed until all problems are fully understood and corrected. Materials produced by the Section are being systematically tested for contamination.
  1. Of the participants in the 46 studies that are potentially affected, approximately 250 are currently scheduled to receive products manufactured by the PDS. NIH has notified the individual principal scientists responsible for each of those protocols, and is in the process of notifying the participants in these protocols. The vast majority of these patients are not immediately due for treatment and NIH is working to secure alternative sources for the products.
  1. An external group of experts in microbiology and sterile manufacturing practices will be appointed to conduct a thorough review, including an assessment of all standard operating procedures, policies, staffing, and training, and make recommendations to the NIH director on the corrective actions required.
  1. In addition to the immediate steps NIH is taking, it will provide an interim corrective action plan to the FDA by Friday, June 19, 2015.
“Our first responsibility is the safety and care of our patients,” said Dr. Collins. “NIH leadership is determined to identify and correct all of the deficiencies that have led to this situation.”

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