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Motrin Related Discomfort

Official Government Database Reports36
Online Conversations8
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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: Abdominal distension, Discomfort, Muscle disorder, Abdominal distension, Discomfort, Muscle disorder

Posted By Anonymous in askapatient.com on March 25, 2010 @ 12:00 am

Side Effects: Severe discomfort of upper abdomen and extreme bloating. Could not wear my normal clothes without extreme discomfort. Clearly no digestive issue; but did not know what it was until re...

Druginformer Identified Side Effects: Abdominal distension, Discomfort, Muscle disorder, Abdominal distension, Discomfort, Muscle disorder

Posted By Anonymous in askapatient.com on March 25, 2010 @ 12:00 am

Side Effects: Severe discomfort of upper abdomen and extreme bloating. Could not wear my normal clothes without extreme discomfort. Clearly no digestive issue; but did not know what it was until re...

Druginformer Identified Side Effects: Flatulence, Abdominal distension, Depression, Discomfort, Flatulence, Abdominal distension, Depression, Discomfort

Posted By Anonymous in askapatient.com on January 4, 2008 @ 12:00 am

Side Effects: upper stomach (ribcage) type pain, bloated feeling, gas - very uncomfortable. appitite gain, depression Worked great, but 6 hours later left a feeling of nausea or pain in abd...

Druginformer Identified Side Effects: Flatulence, Abdominal distension, Depression, Discomfort, Flatulence, Abdominal distension, Depression, Discomfort

Posted By Anonymous in askapatient.com on January 4, 2008 @ 12:00 am

Side Effects: upper stomach (ribcage) type pain, bloated feeling, gas - very uncomfortable. appitite gain, depression Worked great, but 6 hours later left a feeling of nausea or pain in abd...

Druginformer Identified Side Effects: Back pain, Headache, Disability, Discomfort, Weight increased, Back pain, Headache, Disability, Discomfort, Weight increased

Posted By Anonymous in askapatient.com on March 14, 2007 @ 12:00 am

... relieved the pain of a low backache. On the 3rd day I begin to get a very sick background headache. On the 4th day, it was horrific, far worse than the debilitating back ache. Can anyone e...

Druginformer Identified Side Effects: Back pain, Headache, Disability, Discomfort, Weight increased, Back pain, Headache, Disability, Discomfort, Weight increased

Posted By Anonymous in askapatient.com on March 14, 2007 @ 12:00 am

... relieved the pain of a low backache. On the 3rd day I begin to get a very sick background headache. On the 4th day, it was horrific, far worse than the debilitating back ache. Can anyone e...

Druginformer Identified Side Effects: Flatulence, Pain, Abdominal distension, Discomfort, Decreased appetite, Flatulence, Pain, Abdominal distension, Discomfort, Decreased appetite

Posted By Anonymous in askapatient.com on December 28, 2004 @ 12:00 am

Side Effects: upper stomach (ribcage) type pain, bloated feeling, gas - very uncomfortable. Loss of appetite

Druginformer Identified Side Effects: Flatulence, Pain, Abdominal distension, Discomfort, Decreased appetite, Flatulence, Pain, Abdominal distension, Discomfort, Decreased appetite

Posted By Anonymous in askapatient.com on December 28, 2004 @ 12:00 am

Side Effects: upper stomach (ribcage) type pain, bloated feeling, gas - very uncomfortable. Loss of appetite


* 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.