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Singulair Related Major depression

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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: Memory impairment, Headache, Nausea, Sinusitis, Obsessive-compulsive disorder, Hepatic congestion, Insomnia, Muscle spasms, Major depression

Posted By Anonymous in askapatient.com on February 10, 2011 @ 12:00 am

Side Effects: This is by far the scariest med I have ever taken. On the positive side, it did give a minor improvement to sinus and bronchial congestion, but the side effects were enormous: headaches...

Druginformer Identified Side Effects: Mood swings, Anger, Anxiety, Cardiac flutter, Major depression, Adverse drug reaction, Heart rate abnormal

Posted By Anonymous in askapatient.com on January 10, 2011 @ 12:00 am

... of bleakness/no hope Worked wonderfully for asthma relief, however, absolutely would NOT ever take again due to horrific side-effects ... could not control mood swings. Was uncontrollably d...

Druginformer Identified Side Effects: Disturbance in attention, Rash, Vision blurred, Major depression, Suicidal behaviour

Posted By Anonymous in askapatient.com on May 3, 2010 @ 12:00 am

Side Effects: Prevously took 5 mg on & off for 3-4 year, but when dosage was bumped up to 10 mg, had major depression, suicidal tendencies, lack of concentration, poor vision and trouble relating to ...

Druginformer Identified Side Effects: Anxiety, Mood altered, Somnolence, Major depression

Posted By Anonymous in askapatient.com on April 19, 2008 @ 12:00 am

Side Effects: Depression,anxiety,mood changes,fatigue I took singular for 10 years and suffered major depression, anxiety. All these years I though it was from menepause or or just a family...


* 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.