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Singulair Related Visual impairment

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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, Sinus headache, Visual impairment, Ear pain

Posted By Anonymous in askapatient.com on March 11, 2013 @ 12:00 am

Side Effects: None with brand singulair. Since going on generic, I have had ear pain, headachs, blured vision, and sinus pressure. Will be contacting Doctor in the morning.

Druginformer Identified Side Effects: Alopecia, Injury, Arthralgia, Wheezing, Mood swings, Visual impairment, Vision blurred

Posted By Anonymous in askapatient.com on October 18, 2012 @ 12:00 am

Side Effects: hair loss, mood swings, blurry spot in my right eye, joints ache, and have had a few joint related injuries. it has controlled my wheezing and keeps me from getting the headac...

Druginformer Identified Side Effects: Paranoia, Nightmare, Tinnitus, Crying, Visual impairment, Depression, Psychotic disorder

Posted By Anonymous in askapatient.com on April 24, 2007 @ 12:00 am

... of time and not know why, worried all the time, severe nightmares, unable to distinguish between imagined thoughts and real events, they just started to blur together, paranoid (thinking people were 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.