Blood Pressure Drug Recalls Reveal Global Manufacturing Problems

Published November 21, 2018
By Anonymous

Last week, another blood pressure drug recall was announced, the third since July. Losartan is the latest drug to be recalled for possible nitrosamine contamination, a class of chemicals that may cause cancer. It follows the recalls of irbesartan earlier in November, and valsartan in July.

Nitrosamines are naturally occurring chemicals used in gasoline, rocket fuel, plastics, and other industrial materials. Losartan and irbesartan were both found to be contaminated with NDEA, while valsartan contained trace amounts of a related substance, NDMA. It’s believed that the NDEA and NDMA that tainted the blood pressure drugs were byproducts of flawed manufacturing processes.

How are these recalls connected? And why have so many been announced recently? To answer that, we looked at the source: their manufacturers. 

Recalls Show Our Dependence on China, India 

Losartan and valsartan are both made by Chinese manufacturer Zhejiang Huahai Pharmaceuticals, while irbesartan is made by Indian pharmaceutical manufacturer Aurobindo.

This is typical for pharmaceutical drugs sold in the U.S. In 2012, experts estimated that 80% of ingredients in U.S. pharmaceuticals are made abroad, and 40% of finished pharmaceutical drugs are made outside the U.S. It’s likely that these numbers are higher now as 80% of the active ingredients in U.S. medicine comes from China and India alone.

Serious adverse drug effects and recalls aren’t unheard of in the U.S., a country with many safety regulations and product liability laws. So what happens when we rely on countries like China and India, who have fewer consumer protection laws and safety standards, to make our medications? How much do we really know about the quality of pharmaceutical drugs we import into the country?

FDA Ramps up the Number of Inspections, but Does It Matter?

In May 2017, the manufacturer of losartan and  valsartan received a warning letter from the FDA.

FDA Commissioner Scott Gottlieb said in a statement from the FDA that these recalls are a sign of greater FDA scrutiny of our foreign drug supply. The agency has opened offices in China, India, Europe, and Latin America to help oversee foreign drug manufacturing. They also announced that they have increased the number of foreign inspections they conduct each year, which now exceeds the number of domestic FDA inspections.

As the number of FDA inspections increases, so do the number of warning letters to drug manufacturers. In 2016, 44 warning letters were sent to Chinese and Indian manufacturers, and in 2017, 61 warning notices were issued.

But, are these inspections and warnings actually making drugs safer, or are they just public actions that look like we’re managing the problem?

In the case of Zhejiang Huahai Pharmaceuticals, which makes losartan and valsartan, an FDA inspection didn’t do much good. In May 2017 the company received a warning letter from the FDA that their drugs did not meet U.S. quality standards after a problematic inspection.

A similar incident happened at Sichuan Friendly Pharmaceutical which received a warning letter from the FDA in June 2018 for their failure to meet safety standards. Two months later, Westminster Pharmaceuticals recalled their thyroid drugs Levothyroxine and Liothyronine, citing quality issues with the ingredients they used from Sichuan Friendly Pharmaceutical.

"FDA inspections are like a parent telling a child to clean his or her room."

“Inspections don't guarantee quality medicines," Rosemary Gibson, author of China Rx and Senior Advisor at The Hastings Center, told us. "There has to be a culture of quality. FDA inspections are like a parent telling a child to clean his or her room. Unless a neat and orderly room is internalized, inspections can't assure quality.”

And sometimes, manufacturers outright lie to FDA inspectors.

In 2013, Ranbaxy Laboratories in India, a large supplier of generic drugs used in the U.S., agreed to pay $500 million in criminal and civil penalties after an eight-year investigation uncovered falsified records and failure to meet multiple drug safety standards. In 2016, Chinese-based Xiamen Origin Biotech was also caught lying to FDA inspectors when they falsely reported that they had stopped relabeling drugs in January 2015, when in fact they were still distributing them one year later.

What Responsibility Do U.S. Companies Have?

"The recalls reveal the failure of companies that purchase active ingredients from Chinese companies."

Author and healthcare reform expert Rosemary Gibson told us that these recalls reveal multiple failures in our drug supply, and the blame doesn't just lie with the FDA.

“First, the recalls reveal the failure of companies that purchase active ingredients from Chinese companies. The buck stops with them.”

“As noted in China Rx, companies have foremost responsibility to assure their suppliers are supplying quality medicines. The importing companies failed to thoroughly assess: 1) the companies they buy from; 2) the manufacturing plants where they are made in China and the chemical processes used in manufacturing; and 3) the products they purchase. The companies that outsource to China have to regain control over manufacturing.”  

“Globalization is de facto deregulation when manufacturing is outsourced to countries that don't have a quality culture that Americans have come to expect.”  

Unless Safety Becomes a Priority, Dangerous Drugs Will Continue to Exist

If things remain the way they are, we’ll likely see more problems with other pharmaceutical drugs in the future.

“As long as the profit motive exists in a culture where safety is not job no.1, Americans will have to suffer through more toxic drugs."

“As long as the profit motive exists in a culture where safety is not job no.1, Americans will have to suffer through more toxic drugs," said Rosemary Gibson. "In the valsartan case, the change in the chemical process that resulted in the presence of a carcinogen was triggered by the intent to optimize the manufacturing process, reduce waste, and increase profitability.”

“The question is how quickly will we know a drug contains a toxic ingredient? The contaminated valsartan was on the market for four years before it was reported. What if the affected drug is a last resort antibiotic for life-threatening infections like MRSA or sepsis?”

“Now, China is ramping up production of generic drugs made by Chinese companies, and China Rx is the first book to name these generic drugs. As our dependence on China increases, there's bound to be more trouble ahead.”  

Don't Let Drug Companies Cut Corners

Too often companies put profits ahead of patient safety. If you or a loved one were injured after taking a pharmaceutical drug, we'd like to hear from you. You may be able to hold the drug manufacturer accountable in the form of a lawsuit.