No link between Chantix and mental health problems says FDA

According to federal health officials this Monday Pfizer's anti-smoking drug Chantix – known as Varenicline, did not increase psychiatric problems like depression and suicidal thoughts in two studies, though the findings are not definitive.

Chantix works by binding to the same spots in the brain that nicotine does when people smoke, blocking nicotine from those spots but causing release of a “feel-good” chemical, dopamine. The drug's label already carries a boxed warning, the most serious type, listing possible side effects including hostility, agitation, depression and suicidal thoughts and behavior.

The Food and Drug Administration have been investigating reports of mood disorders and erratic behavior among Chantix patients since 2007. The agency said in a statement that two federally-funded studies involving more than 26,000 patients did not show an increased rate of psychiatric hospitalizations among Chantix patients, compared with those using nicotine patches and smoking cessation treatments.

The Veterans Affairs study included 14,131 Chantix users and an equal number of nicotine replacement therapy users. Sixteen Chantix-treated patients were hospitalized for psychiatric reasons compared to 21 in the replacement therapy group.

The Pentagon studied 11,978 Chantix users and an equal number of replacement therapy patients. Patients on Chantix were hospitalized 18 times for psychiatric reasons compared to 16 times among replacement therapy patients.

However the FDA mentioned that the studies only recorded psychiatric problems that resulted in hospitalization, meaning many issues likely went unreported. Additionally, the studies by the Department of Veterans Affairs and the Department of Defense were not large enough to pick up very rare side effects. Groups like the Federal Aviation Administration have already banned the drug for pilots and air traffic controllers due to side effects that could interfere with their work.

The agency is continuing to study the problems and recommends patients consult their doctors if they experience side effects with the drug. Pfizer is conducting its own large-scale study of Chantix behavioral effects, but the results won't be available until 2017.

“Healthcare professionals should advise patients and caregivers that the patient should immediately stop taking Chantix and contact a healthcare professional if agitation, hostility, depressed mood, or changes in behavior or thinking that are not typical for the patient are observed,” the FDA said in an online statement.

More than 8.9 million people in the U.S. have filled prescriptions for Chantix since it was approved in May 2006. Last year Pfizer reported $755 million in sales for the drug, a decline of 14 percent since its peak sales of $883 million in 2007.

“We are reviewing this important information for smokers provided by the FDA,” MacKay Jimeson, a spokesman for Pfizer said. “Given the significant public health risks of smoking, Chantix is an important treatment option for adult smokers to help patients stop smoking.”

Dr. Ananya Mandal

Written by

Dr. Ananya Mandal

Dr. Ananya Mandal is a doctor by profession, lecturer by vocation and a medical writer by passion. She specialized in Clinical Pharmacology after her bachelor's (MBBS). For her, health communication is not just writing complicated reviews for professionals but making medical knowledge understandable and available to the general public as well.

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Comments

  1. Lowell Norby Lowell Norby United States says:

    Thats right FDA cover your ass, your the one that aproved It. You say the report Is In conclusive..Another time you cover your ass.Chantix wont hace the report untill 2017,after the statue off limatations.Runs out of course Its not ass bad now bec use you have change the dosing..When Im finished with the hospital Im coming after you..I dont enjoy anything any more .Took It In 2008 for five days lucky to be alive or am I ?

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