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Hytone

Ingredients: Hydrocortisone
Average User Review Score
* Based on 0 reviews from across the web.
Wikipedia

Cortisol is a steroid hormone, in the glucocorticoid class of hormones, and is produced in humans by the zona fasciculata of the adrenal cortex within the adrenal gland. It is released in response to stress and low blood-glucose concentration.

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* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

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Druginformer Identified Side Effects: None

Posted By 100001540470979 in facebook.com on May 30, 2012 @ 12:00 am

Oral steriods are too difficult to stop. Our experience with rebound was a nightmare and I hope to never use oral steroids again. We use Hytone daily. Hytone is a rx that is Aquaphor with 2.5 hydroco...

Druginformer Identified Side Effects: None

Posted By Anonymous in facebook.com on June 2, 2011 @ 12:00 am

Stephanie My daughter is 7, but at about 5, she would break out in hives after her bath. With a lot of internet research, I realized it was the temperature in the tub. We always run the bath as cool a...

Druginformer Identified Side Effects: None

Posted By lmwolf in drugs.com on June 2, 2007 @ 12:00 am

eed help finding drug My son's pedi gave me a presc for 'hytone 1%'. I have been unable to find this at my local pharmacies. I was just looking online and can only find 2.5%. Can anyone help me find...


* 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.