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Hc (hydrocortisone)

Ingredients: Hydrocortisone
Average User Review Score
* Based on 3 reviews from across the web.
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  Please use Workbench for in-depth research on Hc (hydrocortisone).

Common adverse events from online conversations
Common adverse events from FDA database
* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

Tell us about your Experience with Hc (hydrocortisone)

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Druginformer Identified Side Effects: Drug ineffective

Posted By Anonymous in drugs.com on October 18, 2010 @ 12:00 am

Anucort-HC (hydrocortisone) for Psoriasis: Keeps skin moist and keeps from cracking, but does nothing to reduce other symptoms.

Druginformer Identified Side Effects: None

Posted By Anonymous in drugs.com on September 17, 2010 @ 12:00 am

Proctosol-HC (hydrocortisone) for Hemorrhoids: Almost immediate relief, long lasting.

Druginformer Identified Side Effects: None

Posted By Anonymous in drugs.com on December 26, 2009 @ 12:00 am

Proctosol-HC (hydrocortisone) for Hemorrhoids: Much better than Preparation H or any other type of Hemorrhoid Cream

Druginformer Identified Side Effects: None

Posted By jack54 in healingwell.com on December 29, 2014 @ 12:00 am

Thanks everyone. I've got some Anusol-HC (hydrocortisone) suppository that the docs think will quell the irritation and the spasms. [after 3 weeks, finally a conversation with the docs! note to other...

Druginformer Identified Side Effects: None

Posted By ButtonButton in mdjunction.com on March 5, 2013 @ 12:00 am

The dosing equivalency of prednisone and HC is roughly: 1 mg of prednisone = 4 mg of HC (hydrocortisone). - Karen -


* 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.