I wanted to give everyone the heads up about something that happened today. I take Singulair oral for my allergies and have taken it for 5 years or more. Today I got a letter from my doctor, telling me that the FDA has black boxed Singulair (montelukast) for some pretty gnarly side effects, a lot of them psychological, anxiety, aggressive behavior, vivid nightmares/dreams, tardive dysconesia (geeze I hope I spelled that right) the list was long and scary. He told me to stop taking it NOW!
Weird thing is that I called my pharmacy and talked to a pharmacist. They hadn't gotten a flagged warning for it at all but when he looked it up, yep, he found it and told me that he takes it too but wasn't going to stop unless his doctor told him to......I told him mine had done just that and read him the letter. He couldn't offer any suggestions other to warn me that without it I would notice a worsening of my allergies. Like that would be different? This has been the allergy season from hell so far. But if my doctor said don't take it, I shouldn't take it till I can talk to them.
Wow! Thanks for the warning. I don't take Singulair (montelukast) all the time, but have it on hand, and do take it if I have respiratory issues, an asthma attack, or if I'm in danger of an allergy induced asthma attack. I'll have a chat with my doctor, the next time I go in.
The FDA should require black box warnings on the information inserts of prescriptions, when it applies, but they don't. You are correct about black box warnings not getting out as well as they should, throughout the medical community the way they should.