January 13, 2009

FDA Updates Information Regarding Singulair and its Relation to Suicide

Today the FDA issued further information regarding its investigation between the drug Singulair, a drug used for treatment of asthma and allergies, and suicidal thinking and behavior, as well as suicide itself. I previously wrote about this concern when it was first raised back in March of 2008 here. The FDA has asked manufacturers of all products used to treat asthma and allergies to submit information about suicide related adverse events, as well as mood and behavior related adverse events which the manufacturers of these products had obtained through its clinical trials on these drugs. 444500_self-portrait.jpg


The bottom line so far is that the clinical trial data provided by the pharmaceutical companies, including Merck, the manufacturer of Singulair, does not appear to show a causal relationship between Singulair and issues of suicidality. Only one adult patient out of 9,929 patients treated with Singulair during the clinical trials showed indications of thinking about suicide or what is referred to as suicidal ideation. The FDA is continuing to review this clinical trial data to see if there is any indication of other mood and behavior adverse events related to the drugs and it has not reached any conclusions about whether a causal relationship exists.

The FDA is also looking at post marketing reports of neuropsychiatric events with regard to Singulair, as well as Accolate and Zyflo to compare the Adverse Events for each of these drugs which are somewhat similar. Most of the neuropsychiatric events received thus far are for Singulair and the information provided is consistent with a drug induced effect. The FDA indicates it will continue to evaluate this issue and update it in the near future.

At the very least, it is good to see the FDA being proactive and providing information regarding ongoing investigations. Should further information be forthcoming, I will provide additional posts. If you or someone you know have had suicidal thoughts or feelings while taking the drug Singulair, first contact your physician immediately. Also, make sure you advise the FDA by going to www.fda.gov/medwatch/report.htm.

March 27, 2008

FDA Warns About Suicidality with use of Singulair

Today the FDA published an "early communication" regarding the drug Singulair which is used to treat asthma and allergies. According to the FDA, there is indication that taking of this drug might lead to suicidal thinking and behavior, otherwise known as "suicidality". Here is a drug meant for asthma and allergies and it is causing people to think about killing themselves?!? This is out of control.

I have handled several cases over the last many years involving children and adolescents who have been prescribed anti-depressants such as Paxil and Prozac and killed themselves. I have to tell you, there is no more difficult case to deal with on a personal level than a client who's young innocent child has decided to take their own life. The usual defense raised by the phamaceutical companies is that it was the disease i.e. depression, not the drug which lead the child to kill him or herself. In the cases I handled I was able to successfully show to the pharmaceutical companies that these children were never diagnosed clinically depressed, but instead were prescribed the medication by the family physician because the child was "going through a rough patch" i.e. adolescents. The doctors were lead to believe by the pharmaceutical companies that these anti-depressants were "safe" and promoted the drugs to be used to help those who are feeling "down in the dumps". This was despite the fact the drug was approved by the FDA to be prescribed for diagnosed depression. Thus, I was able to show that there was nothing else which could have caused the child to take the desperate act of suicide but the drug itself.


With Singulair, a drug prescribed for allergies and asthma, Merck, the manufacturer cannot claim the disease called the patient to take his own life. Should be interesting to see how Merck explains this one. Clearly, a patient taking a drug for allergies isn't expecting to feel suicidal. One thing I would say is it appears the FDA is trying to get information out there to the public on safety concerns alot quicker. I have to commend them for that. According to the FDA's website, Merck changed the adverse events on the package insert (what you generally get from the pharmacy when you pick up your prescription) on this drug in October 2007 to include suicidality concerns. They are working with Merck to figure out how to publicize this to the public and to doctors. It has been almost 6 months since they changed the package insert on this drug and they are still trying to figure out how to publicize this to doctors????? Something as significant as potential for suicide ??? Things that make you go "Hmmmm????"