DrugInformer Search

Ibu Related Pain

Official Government Database Reports9
Online Conversations3
Share

Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.


Tell us about your Experience with Ibu

Thank you for sharing your experience with us!

Share Your Experience

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: Pain

Posted By Anonymous in askapatient.com on March 22, 2011 @ 12:00 am

... figure out that the side effects were attributable to the Cialis. I LOVE this drug. It exceeds by far the results with Viagra,But, as others are saying, it is NOT worth tha pain that follows a couple ...

Druginformer Identified Side Effects: Pain, Musculoskeletal pain

Posted By bethster39 in ehealthforum.com

I have had several episodes over the past year where I get this terrible ache/pain in my left shoulder. I have a very, very slow GI system and have attributed this pain to that. I have no trouble pass...


* 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.