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Adapalene Related Drug ineffective

Official Government Database Reports5
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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: Pain, Crying, Hysterical psychosis, Drug ineffective

Posted By Epiduo in drugs.com on April 9, 2014 @ 12:00 am

... cystic acne on my cheeks and I begged my mom to take me to the dermatlogist. Initially he prescribed Atralin which didn't help. It burned my skin and I would cry because it hurt so bad. I used it for ...

Druginformer Identified Side Effects: Drug ineffective

Posted By Anonymous in drugs.com on December 19, 2010 @ 12:00 am

... recommend drinking lots of water if you're on the regimen I am. Need to stay hydrated while using these medicines. Believe me, I'm a registered medical assistant. If Epiduo didn't work, I wouldn't be ...

Druginformer Identified Side Effects: Erythema, Dry skin, Drug ineffective

Posted By Anonymous in drugs.com on December 19, 2010 @ 12:00 am

... to clindamycin lotion and doxycycline and have been using it all for about 5 days. I noticed a difference in my skin the very first day. I am experiencing some dryness and mild redness upon waking in ...

Druginformer Identified Side Effects: Eczema, Drug ineffective

Posted By Anonymous in drugs.com on November 20, 2009 @ 12:00 am

Epiduo (adapalene / benzoyl peroxide) for Acne: I had an unpleasant experience. I had only used it for a week and it made big red marks on my face like eczema. And it didn't help with my acne at all.

* 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.