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Ibu Related Headache

Official Government Database Reports9
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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: Headache, Pain, Flushing, Inflammation, Blindness, Glaucoma, Swelling, Adverse drug reaction

Posted By Anonymous in askapatient.com on August 17, 2011 @ 12:00 am

Side Effects: Facial Flushing, Dull Headaches, Red puffy eyes, pain and pressure in the eyes. I took this drug after my urologist suggested it because of pain in my uretha from a bladder ne...

Druginformer Identified Side Effects: Headache, Myalgia

Posted By Anonymous in askapatient.com on July 1, 2011 @ 12:00 am

Side Effects: Sore muscles, headache I have had anxiety based ED my entire life. Until I tried this product I thought this would be something I just had to live with. With this product I ...

Druginformer Identified Side Effects: Headache, Flushing, Discomfort, Irregular sleep phase

Posted By Anonymous in askapatient.com on September 5, 2007 @ 12:00 am

Side Effects: I have had a headache now for 5 days. It also caused a flushing in my face. There is a discomfort in my upper leg that disrupts sleep (unless I take ibuprophen before bed). I am hesi...

Druginformer Identified Side Effects: Headache, Sinusitis

Posted By Anonymous in askapatient.com on June 28, 2007 @ 12:00 am

Side Effects: Migrane-like headache and slight sinus congestion as medicine absorbs into the sytem. I use 800mg ibuprofine to counter these effects. I love the product! I have to take 2 20 ...


* 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.