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Singulair Related Oral pain

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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: Oral pain, Anxiety, Ear pain, Panic attack, Oropharyngeal pain

Posted By katieb in fdb.rxlist.com on June 2, 2009 @ 12:00 am

I've been on this medication for about 2 months and have experienced an almost constant earache, sore throat and sore mouth. My doctor removed me from it for 2 weeks at one point to see if I felt bet...

Druginformer Identified Side Effects: Aggression, Tremor, Cold sweat, Abdominal discomfort, Oral pain, Somnambulism, Abdominal pain upper, Abnormal dreams, Confusional state, Diarrhoea, Hallucination, Insomnia, Irritability, Restlessness, Decreased appetite

Posted By Anonymous in druglib.com

Aggressive behaviour - hitting me dad and herself badly Bad dreams Confusion Hallucination Irritability Restlessness Sleepwalking Tremors Trouble sleeping oral pain Stomach pa...

Druginformer Identified Side Effects: Hallucination, Tremor, Cold sweat, Abdominal discomfort, Oral pain, Somnambulism, Abdominal pain upper, Abnormal dreams, Aggression, Confusional state, Diarrhoea, Insomnia, Irritability, Restlessness, Decreased appetite

Posted By Anonymous in druglib.com

Aggressive behaviour - hitting me dad and herself badly Bad dreams Confusion Hallucination Irritability Restlessness Sleepwalking Tremors Trouble sleeping oral pain Stomach pa...


* 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.