DrugInformer Search

Singulair Related Euphoric mood

Official Government Database Reports16
Online Conversations3
Share

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: Euphoric mood, Arrhythmia, Dysgeusia, Insomnia, Psychomotor hyperactivity

Posted By Anonymous in askapatient.com on November 12, 2014 @ 12:00 am

Side Effects: Sudden hyperactivity, insomnia all night, racing and erratic heartbeat, feeling very lightheaded and strange, bitter taste in the mouth. Quite a scary experience and not much ...

Druginformer Identified Side Effects: Euphoric mood, Thought withdrawal

Posted By Anonymous in askapatient.com on March 22, 2010 @ 12:00 am

Side Effects: Light headed, "zoned out" I was prescribed Singulair to help combat really bad allergies (very rainy this year, which causes plant population to explode). I notice the first ...

Druginformer Identified Side Effects: Headache, Dizziness, Anxiety, Euphoric mood, Depression, Irritability, Muscle twitching, Paraesthesia

Posted By Anonymous in askapatient.com on March 18, 2009 @ 12:00 am

Side Effects: Dizziness, light-headedness, anxiety, depression, irritability, headaches, twitchy, tingling sensation. My Dr specifically said that it had zero side effects, so I took this f...


* 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.