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Singulair Related Obsessive-compulsive disorder

Official Government Database Reports90
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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: Obsessive-compulsive disorder, Obsessive thoughts, Diarrhoea, Haemoptysis, Hallucination, Haemorrhage

Posted By Anonymous in askapatient.com on December 25, 2011 @ 12:00 am

... was coughing up blood. He flicked on the light and I was fine, but I couldn't shake the feeling. The exact same thing happened once every few days. Last night, I started having OCD thoughts about how ...

Druginformer Identified Side Effects: Feeling abnormal, Obsessive-compulsive disorder, Asthma, Hallucination

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

Side Effects: Asthma is better.. But hallucinating , OCD , feeling weird

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: Nightmare, Anxiety, Obsessive-compulsive disorder, Somnambulism, Hallucination

Posted By Anonymous in askapatient.com on February 2, 2011 @ 12:00 am

Side Effects: Severe Anxiety, Halucinations, OCD type behaviours, Nightmares, sleepwalking. It should be banned!

Druginformer Identified Side Effects: Sleep disorder, Crying, Obsessive-compulsive disorder, Depression, Attention deficit/hyperactivity disorder

Posted By Anonymous in askapatient.com on February 6, 2010 @ 12:00 am

Side Effects: BEHAVIORAL, TANTRUMS, OCD, ODD, MASTURBATION ( YES AT 3 YEARS OLD), DEPRESSION, PROBLEMS SLEEPING, ETC ETC AND ETC. my daughter was sick the whole winter last year, she was ab...

Druginformer Identified Side Effects: Sleep disorder, Anxiety, Obsessive-compulsive disorder, Depression, Phobia

Posted By Anonymous in askapatient.com on January 17, 2010 @ 12:00 am

Side Effects: depression,anxiety,sleep disorder,school phobia,ocd while my son was on this drug,my family and my child went through hell,this drug is poison for some.It is so important that...

Druginformer Identified Side Effects: Abdominal discomfort, Nightmare, Obsessive-compulsive disorder, Screaming, Eye swelling, Tic, Decreased appetite

Posted By Anonymous in askapatient.com on May 23, 2008 @ 12:00 am

Side Effects: Tics, facial and eye swelling,lack of appetite, stomach pains, nightmares, OCD tendencies, uncontrollable screaming bouts sometimes lasting an hour My Grandson is one of the ...

Druginformer Identified Side Effects: Headache, Polyuria, Pain, Nightmare, Obsessive-compulsive disorder, Abnormal dreams, Accidental poisoning, Aggression, Antisocial behaviour, Depression, Hallucination, visual, Mood altered, Suicidal ideation, Compulsions, Negative thoughts

Posted By Anonymous in askapatient.com on April 10, 2007 @ 12:00 am

... or "Bad Thoughts" OCD (obsessive compulsive disorder), very violent thoughts of hurting people or animals, facial ticks, frequent urination, bad dreams, severe headaches, depression, aggression, deep ...

* 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.