Drug Injury
Stewart & Stewart Injury Lawyers
Smoking Drug Chantix® Linked to Depression, Suicidal Behavior
The anti-smoking drug Chantix® has been linked to depression, suicidal thoughts, and violent behavior in some users, according to the Food and Drug Administration (FDA) (1). Government scientists are currently investigating the matter after reports of mood disorders and erratic behavior in some users came to their attention earlier this year.
Chantix Update:
According to researchers, hundreds of patients taking Chantix have reported serious accidents, vision problems, and heart trouble.
The FAA then prohibited its pilots from using Chantix because
of its possible dangers, which also include blurred vision, dizziness,
confusion, loss of consciousness, and a previously established link to suicidal
behavior (source).
Chantix is a prescription drug designed to help adults quit smoking. It comes in a white tablet (0.5mg) and a blue tablet (1mg) and is usually taken for 12 weeks at a time (2).
Chantix may be dangerous to some users. The FDA issued a report that stated, “A preliminary assessment reveals that many of the cases reflect new-onset of depressed mood, suicidal ideation, and changes in emotion within days to weeks of initiating Chantix treatment(1).” Some of the patients who have been adversely affected by Chantix had no history of psychiatric illness and had not quit smoking when they experienced suicidal thoughts.
Update 1/18/08: Chantix will carry more prominent warnings that patients should be monitored for unusual activity including agitation, depression and suicidal behavior. The new warnings will be featured prominently on the anti-smoking drug’s labeling.
The FDA issued the following alert on 2/1/2008: "FDA is issuing this Alert to highlight important revisions to the WARNINGS and PRECAUTIONS sections of the full prescribing information for Chantix regarding serious neuropsychiatric symptoms. Serious neuropsychiatric symptoms have occurred in patients taking Chantix.
These symptoms include changes in behavior, agitation, depressed mood, suicidal ideation, and attempted and completed suicide. While some patients may have experienced these types of symptoms and events as a result of nicotine withdrawal, some patients taking Chantix who experienced serious neuropsychiatric symptoms and events had not yet discontinued smoking.
In most cases, neuropsychiatric symptoms developed during Chantix treatment, but in others, symptoms developed following withdrawal of Chantix therapy."
Our lawyers are committed to helping people affected by Chantix get the legal help they need so that victims can get the compensation they deserve if Chantix use has adversely affected their lives. Call one of our Chantix lawyers today. We want to help.
Chantix® is a registered trademark of Pfizer, Inc. and is used here only to identify the product in question.
Sources:
- Early Communication About an Ongoing Safety Review Varenicline (marketed as Chantix)from the FDA. Accessed 11/30/07 viawww.fda.gov.
- Patient Information Sheet—Varenicline (marketed as Chantix)from the FDA. Accessed 11/30/07 viawww.fda.gov.
This law firm is not associated with, sponsored by, or affiliated with the Food and Drug Administration or Pfizer, Inc.
Free Consultation
contact Stewart & Stewart injury lawyers today!
If you have been injured as a result of pharmaceuticals, contact an Indiana drug injuries lawyer at Stewart & Stewart. We have offices located in Carmel, Greenwood, Marion & Anderson, and we have successfully advocated for clients throughout the area, including Fort Wayne, Gary, Indianapolis, and South Bend. Complete a Free Online Consultation Form or call us at 1-800-333-3LAW today!
Stewart & Stewart
Main Office:
931 S. Rangeline Road
Carmel, Indiana 46032
Phone: 317-846-8999
Fax: 317-843-1991
Other Offices
Click Here
Free Consultation
Complete the following form to be contacted by Stewart & Stewart Personal Injury Lawyers.
Hot Topics
Chantix®
Linked to depression, suicidal thoughts, and violent behavior.
CNN Reveals
Revealed damning evidence against major insurance companies.
Digitek®
The FDA has issued a Class I recall.
Fosamax®
Fosamax®, has been linked to osteonecrosis of the jaw.
Heparin Recall
Urgent recall of units manufactured by Baxter Healthcare.
Hernia Patch Danger
The Patch is used to repair ventral (incisional) hernias.
Medtronic Sprint Fidelis
Malfunction leads to health concerns.
MRI Dye (NSF)
A dye used in MRI and MRA scans linked to a fatal skin disease.
Ortho Evra®
Women using Ortho Evra are at an increased risk for fatal blood clots.
Paxil®
The FDA notified professionals of changes to Paxil.
ReNu & Fusarium Keratitis
Linked to Severe Eye Infections.
Seroquel®
A drug in the class of atypical antipsychotics approved by the FDA.