DrugInformer Search

Singulair Related Abnormal sleep-related event

Official Government Database Reports11
Online Conversations3

Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.

Tell us about your Experience with Singulair

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Nightmare, Mood altered, Appetite disorder, Abnormal sleep-related event

Posted By Anonymous in askapatient.com on August 5, 2009 @ 12:00 am

Side Effects: dramatic mood change= went from wonderful temperment to hair trigger trantrums, sleeping changes= nightmares and sleeping patterns, change in appetite= eat anything & everything to very...

Druginformer Identified Side Effects: Fatigue, Sleep disorder, Nightmare, Depressed mood, Mood altered, Abnormal sleep-related event

Posted By Anonymous in askapatient.com on July 15, 2007 @ 12:00 am

Singulair has worked very well to control asthma and allergy symptoms. Personally, I have not experienced nightmares or leg cramps. But read on... I have been taking it for probably a...

Druginformer Identified Side Effects: Hunger, Abnormal weight gain, Influenza, Apathy, Disturbance in attention, Muscular weakness, Somnolence, Weight increased, Abnormal sleep-related event

Posted By Anonymous in askapatient.com on April 10, 2007 @ 12:00 am

... much of anything. I go to work and sometimes struggle with simple instructions or can't carry on conversations intelligently due to lack of concentration. I'm just too tired and hungry most of the tim...

* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.