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Singulair Related Hyperventilation

Official Government Database Reports40
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.

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Druginformer Identified Side Effects: Nightmare, Memory impairment, Hyperventilation, Abnormal dreams, Drug ineffective, Paraesthesia, Somnolence, Poor quality sleep

Posted By Anonymous in askapatient.com on January 2, 2014 @ 12:00 am

... time of the day that I was taking it, and it didn't help. I came across these pills last night and decided to try one, not remembering if this was the medicine that caused the nightmares (I've tried a...

Druginformer Identified Side Effects: Photophobia, Hypersomnia, Nightmare, Crying, Anxiety, Hyperventilation, Abnormal dreams, Death, Hallucination, Insomnia, Panic attack, Restlessness, Emotional distress, Fear

Posted By Anonymous in askapatient.com on January 23, 2013 @ 12:00 am

... each other all the time about everything, crying very easy, both started talking more about death and had a lot of deep questions about it. They were both getting very sensitive about things and very ...

Druginformer Identified Side Effects: Blepharospasm, Hyperventilation, Aggression, Psychomotor hyperactivity, Restlessness, Thought blocking

Posted By Anonymous in askapatient.com on May 8, 2008 @ 12:00 am

... agressiveness. My son was prescribed Singulair a few years ago. I wish I had found this site sooner. Over the last two years he has been experiencing body tics, eye tics and now breathing t...

* 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.