Plans to slash medical costs in the US run into generic drug concerns
As U.S. regulators push hundreds of new generic drugs to market in an effort to drive down prices, the industry is facing a continuing problem in India, where many copycat medicines are manufactured.
The Food and Drug Administration approved a record 763 generic drugs in the year ending in September 2017. It expects to sign off on even more rivals for branded drugs in 2018. FDA Commissioner Scott Gottlieb has vowed to tackle a lack of competition he has said is “a root cause of high drug prices.”
But getting more low-cost medicines to pharmacy shelves could strain a global supply chain already confronting questions about quality and safety — especially in India, where about 40 percent of generic drugs taken by Americans are made.
The FDA’s efforts to police Indian drug plants have been hampered by staffing shortages as well as aggressive tactics by drug-company employees to cover up potential problems. FDA reports show some workers in India destroyed records to keep regulators in the dark about production issues.
Those oversight gaps could widen as the FDA tries to create a deeper market and companies seek to preserve their profits.
“We’ve increased our focus on data-integrity issues. The fact that we’re unearthing more data-integrity issues, it means there were problems that were systemic and the FDA is starting to crack down,” said Gottlieb in an interview.
Paper Trail
FDA inspection reports from India read like mystery novels full of deleted data, shredded documents and evasive employees. Intrigue surrounds tests designed to ensure that generic drugs are free of contaminants, properly formulated, and work like the products they mimic. When those tests fail, evidence has often vanished or been conveniently invalidated, agency records show.
In a March 2017 visit to a Dr. Reddy’s Laboratories Ltd. plant in Andhra Pradesh, a state bordering India’s southeastern coast, two FDA inspectors caught lab employees deleting computer files and lists of recent documents to avoid detection. Company officials initially denied that workers destroyed the data but capitulated when pressed by inspectors.
The facility continues to manufacture drugs for the U.S. market. The FDA typically gives companies time to fix issues uncovered during an inspection before banning products from the U.S.
“Over multiple days in multiple departments we were provided false and misleading answers to the questions that we asked employees,” the inspectors wrote in a report released Jan. 3. “The pattern of providing false and misleading statements persisted throughout the inspection.”
The inspection, which yielded more than 50 pages of observations detailing data discrepancies and failures to follow proper manufacturing standards, was a follow-up to a 2015 visit to the same plant, after which the FDA warned Dr. Reddy’s over many of the same practices.
Dr. Reddy’s declined to comment.
Enforcement Struggle India’s drug-manufacturing problems go back years. In 2013, Ranbaxy Laboratories Ltd., which was later bought by Sun Pharmaceutical Industries Ltd., agreed to pay $500 million to resolve allegations it sold adulterated drugs and lied about it to U.S. regulators.
Two of the plants Sun bought in that deal still aren’t permitted to send products to the U.S. Another Sun facility has been on the FDA’s banned list since 2014 after deleting more than 5,000 potentially undesirable tests.
In all, the FDA lists 44 drugmanufacturing facilities in India that are banned from sending products to the U.S.
Despite vowing to step up inspections, the FDA has struggled to monitor the more than 500 facilities in India registered to make drugs for the U.S. Agency inspections there dropped 27 percent in fiscal 2017 from a year earlier, to 185 from 252.
The FDA’s New Delhi office was authorized to have 13 investigators but only three slots were filled as of July 16, 2016, according to a Government Accountability Office report last year.
The number of inspections the FDA does each year can fluctuate, as does its staffing levels, Lauren Smith Dyer, an agency spokeswoman, said in an email. The agency determines which drugmakers to inspect based on known safety risk that takes into account compliance history as well as the type of products being manufactured.
“We think we’re much more effective at targeting those inspections now,” said Gottlieb, the FDA chief.
Data integrity
India’s pharmaceutical industry has improved the sanitation issues that plagued it when the FDA began increasing resources there; inspection reports no longer feature fly infestations and drains spilling over with urine. But assuring that the data reported to the FDA is fair and accurate and that important results haven’t been concealed still appears to be a problem.
In November, the FDA warned two Indian facilities operated by Lupin Ltd. for ignoring tests showing that pills made there didn’t meet quality standards. In 2015 and 2016, the FDA found 134 instances when drugs or active ingredients failed initial testing but the company chose to override the results. Lupin called the failed tests “laboratory error” even when evidence suggested that wasn’t the case, according to the FDA.
Lupin has 11 facilities that manufacture generics globally, according to its website. Its products include widely prescribed antibiotics, oral contraceptives and cardiovascular and depression drugs. According to a review of generic versions of depression drug Cymbalta by Bloomberg News last year, Lupin’s was the subject of the most complaints to the FDA.
Lupin didn’t respond to a request for comment.
Global repercussions
Big foreign drugmakers such as Mylan NV, incorporated in the Netherlands, and Fresenius SE, headquartered in Germany, also received warnings about their manufacturing facilities in India. Mylan employees at its Maharashtra plant failed to investigate why drugs there didn’t meet quality standards and didn’t report substandard test results, according to the FDA.
“Consumers have no reason to be concerned by the quality of Mylan drugs manufactured in India,” Lauren Kashtan, a Mylan spokeswoman, said in an email. Mylan believes it has addressed the FDA’s concerns “and are awaiting re-inspection very soon,” she said.