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Singulair Related Menstruation irregular

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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: Rhinitis, Emergency care, Acne, Depression, Varicella, Suicidal behaviour, Menstruation irregular

Posted By Anonymous in askapatient.com on August 19, 2013 @ 12:00 am

... almost institutionalised for my safety), and was also now having varicella spots breaking out on my arms and side. My GP told me to stop the drug IMMEDIATELY! No amount of rhinitis symptom relief is w...

Druginformer Identified Side Effects: Tremor, Pruritus, Anxiety, Insomnia, Menstruation irregular

Posted By Anonymous in askapatient.com on March 5, 2013 @ 12:00 am

took 2 different times. wasn't sure what med was my problem. started cortef same time. last time took 3 days. head itching,red spots in scalp,flaking, BP went up, can't sleep, shaking,...

Druginformer Identified Side Effects: Polyuria, Pruritus, Nightmare, Sneezing, Cough, Drug effect increased, Rash, Emotional distress, Menstruation irregular

Posted By Anonymous in askapatient.com on April 20, 2009 @ 12:00 am

Side Effects: rash, cough, sneezing, attitude problems, frequent urination, nightmares, emotional outbursts My four year old was put on this medication while with her other parent. She was ...


* 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.