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Singulair Related Listless

Official Government Database Reports14
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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: Headache, Dizziness, Anxiety, Abdominal pain upper, Confusional state, Depression, Irritability, Listless, Mood altered, Poor quality sleep, Suicidal behaviour

Posted By Anonymous in askapatient.com on July 5, 2012 @ 12:00 am

Side Effects: Increased anxiety, restless sleep, headaches, stomach aches, despondency/depression, suicidal thinking I've always been a very solid, happy person with very predictable moods....

Druginformer Identified Side Effects: Feeling cold, Aggression, Hallucination, Listless, Rhinorrhoea

Posted By Anonymous in askapatient.com on May 15, 2010 @ 12:00 am

Side Effects: NEGATIVE SELF-TALK, AGGRESSIVE BEHAVIORS, GENERAL NEGATIVITY, LISTLESSNESS, SLEEP HALLUCINATIONS FOR 2 WEEKS AFTER STOPPING DRUG - NORMAL KID NOW! MY SON IS 5YEARS OLD AND IS...

Druginformer Identified Side Effects: Aggression, Hallucination, Listless, Suicidal behaviour

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

Side Effects: negative self-talk, suicidal vocabulary, aggressive behaviors, general negativity, listlessness, sleep hallucinations for 5 weeks after stopping drug - NORMAL KID NOW! Do NOT ...

Druginformer Identified Side Effects: Mood swings, Anxiety, Sudden death, Listless, Somnolence, Fear

Posted By Anonymous in askapatient.com on February 26, 2008 @ 12:00 am

Side Effects: mood swings, dpression, anxiety, fears, fatigue, listlessness at times my now 5 year old son was prescribed this drug over 2 years ago. we recently have had issue with some ve...


* 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.