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Singulair Related Syncope

Official Government Database Reports307
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Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.

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Druginformer Identified Side Effects: Syncope, Anger, Frustration, Depression, Insomnia, Irritability

Posted By Anonymous in askapatient.com on April 26, 2013 @ 12:00 am

Side Effects: Anger, frustration, angst, introversion, depression, fainting My son began taking Singulair when he was 7. We were warned about behavioral issues (ADD like symptoms, insomnia...

Druginformer Identified Side Effects: Syncope, Anxiety, Apathy, Irritability, Mood altered, Suicidal ideation

Posted By Anonymous in askapatient.com on January 21, 2013 @ 12:00 am

Side Effects: Severe anxiety attacks-even at home for no apparent reason, irritability, sadness, lack of interest, unusual thoughts of death, feelings as though I were going to faint

Druginformer Identified Side Effects: Arthralgia, Joint swelling, Syncope, Myalgia, Disability, Dyspnoea, Muscular weakness

Posted By Anonymous in askapatient.com on March 11, 2010 @ 12:00 am

Side Effects: For eight months, I experienced debilitating knee pain. I needed crutches for five months. I fainted a few weeks ago and I discovered that symptoms like my horrible knee pain were simil...

* 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.