The medicine Singulair, are the side effects more dangerous than they let on  | | The Food and Drug Administration said Thursday it is investigating a possible link between Merck's best-selling Singulair and suicide. FDA said it is reviewing a handful of reports involving mood changes, suicidal behavior and suicide in patients who have taken the popular allergy and asthma drug.
Merck has updated the drug's labeling four times in the past year to include information on a range of reported side effects: tremors, anxiousness, depression and suicidal behavior.
With sales of $4.3 billion last year, Singulair is used by millions of patients in the U.S, according to Merck. First approved in 1998, it's part of a class of asthma and allergy drugs that includes AstraZeneca's Accolate and Critical Therapeutics's Zyflo.
FDA said it is also reviewing reports of side effects with those drugs. Their labeling does not contain language about suicide
This is just scary. My son was on this medicine not even 6 months ago, because he gets signs of asthma everytime he gets sick. I took him off the medicine because of the way he was acting. The doc had told me that he might get moody from it. Well he ended up going after me, mind you he's only 6. I called my mom and she said to just watch him the next few days while he was on the medicine. Well than he went after me again. It was like this dark side of him I had never seen before, his eyes glazed over and he didn't realize what he was doing till after he did it. I stopped giving him the medicine right after that. It's scary cause so many kids are on this medicine.
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| | | | | | | | 1. ltmoon (849) | 2 years ago | The FDA is often slow to act against the major pharmaceutical companies. I would be concerned about the Singulair risks that have been revealed so far. If you or someone in your family is using this drug you should contact your physician and talk them about the risks and what other options are available for treatment.
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| | 2. Mcbuttero (859) | 2 years ago | I read about that! Scary. My son used to take that for his asthma. He hasn't taken it in about 4 years... but he's an emotional child anyways (adhd)... and I couldn't imagine what could have happened had it adversly affected him.
What's bad is they aren't allowed to test children before a med is put out there... so they start prescribing it for kids, not knowing what the results will be for them. I think it's irresponsible, and would like them to figure out an alternative before they make my child a guinea pig!
My son was taken off of Strattera (for adhd) over a year ago because apparently there was a "blackbox" warning put out by the FDA... saying that Strattera can cause liver damage. We had switched doctors and the new one informed us of it and had his blood tested. He was fine, but I'm still wondering why the last idiot doctor didn't see the warning?! I guess that's why we switched docs though... I didn't care for the last one! He was too quick to prescribe meds and didn't do a lot of actual "examining."
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