DrugInformer Search

Singulair Related Premenstrual syndrome

Official Government Database Reports6
Online Conversations2

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

Tell us about your Experience with Singulair

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Pruritus, Anxiety, Premenstrual syndrome, Depression, Irritability, Loss of libido, Mood altered, Suicidal ideation, Emotional distress, Negative thoughts

Posted By Anonymous in askapatient.com on June 18, 2008 @ 12:00 am

... Singulair (10mg) and Zyrtec (5mg) which had been prescribed for my asthma and allergies. After about two days of a real funk (withdrawal) and two weeks of extremely itchy skin (Zyrtec withdrawal) I b...

Druginformer Identified Side Effects: Fatigue, Dizziness, Nausea, Vomiting, Nightmare, Memory impairment, Anxiety, Premenstrual syndrome, Decreased interest, Depression, Discomfort, Heart rate increased, Hypertension, Insomnia, Irritability, Migraine, Suicidal ideation, Weight decreased

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

... nightmares, insomnia, irritability, constant PMS type symptoms, migraines (sick migraines - puking), dizziness, nausea, forgetfulness, anxiety, rapid heartbeat, exhaustion, loss of interest. ...

* 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.