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Singulair Related Abdominal pain lower

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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: Eye pruritus, Heart rate abnormal, Headache, Agitation, Anger, Abdominal pain lower, Abdominal pain upper, Diarrhoea, Mood altered

Posted By Anonymous in askapatient.com on March 7, 2015 @ 12:00 am

... Effects: Heart pounding, headaches,angry,aggitated,sad, bad stomach aches lower abdominal pain and diarrhea all thru the day Helped a little with runny nose and itchy eyes but not worth the...

Druginformer Identified Side Effects: Constipation, Pruritus, Abdominal pain lower

Posted By Anonymous in askapatient.com on January 15, 2015 @ 12:00 am

Side Effects: Constipation, Lower Abdominal Pain, Increased Itching

Druginformer Identified Side Effects: Back pain, Headache, Mood swings, Crying, Abdominal pain lower, Abnormal dreams, Bite, Depression, Hallucination, Mood altered, Somnolence, Suicidal behaviour

Posted By Anonymous in askapatient.com on December 26, 2010 @ 12:00 am

Side Effects: Suicide attempt, depression, scary dreams, mood swings, easily crying, hallucinations, headache, abdominal pain, lower back pain, sadness, biting nails and fingers, fatigue ou...


* 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.