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Differin Related Eye swelling

Official Government Database Reports7
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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: Pruritus, Burning sensation, Hypersensitivity, Depression, Eye swelling, Hyperhidrosis

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

Side Effects: Itching, burning, red and swollen eyes with increased sensitivity to any other products. Miserable. Have experienced these awful side effects off and on during my usage; could...

Druginformer Identified Side Effects: Pruritus, Eye swelling, Rash

Posted By Anonymous in askapatient.com on May 15, 2011 @ 12:00 am

Side Effects: Itchy and red, puffy eyelids. Itchy, bumpy, rash on neck. Face seemed a bit puffy as well. Differin did appear to help with my acne. However, due to the side effects described...

Druginformer Identified Side Effects: Pain, Pruritus, Burning sensation, Eye swelling, Swelling

Posted By Anonymous in askapatient.com on February 3, 2010 @ 12:00 am

... I use a pea sized amount,twice a week, only on effected areas, nowhere near my eyes and when I woke up on morning my eyes were like two massive puffs.Red, itchy, painful. Swelling lasted 1 w...

Druginformer Identified Side Effects: Dry skin, Eye swelling, Oedema, Skin exfoliation

Posted By Anonymous in askapatient.com on April 24, 2009 @ 12:00 am

Side Effects: Peeling, dry skin, flaking, eye swelling KEEP THIS AWAY FROM YOUR EYES. I can't stress this enough. It says so on the package and in the drug information. I had been using it ...

* 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.