HYDROCORTISONE ACETATE- hydrocortisone acetate suppository
Central Texas Community Health Centers
Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Each suppository for rectal administration contains 25 mg hydrocortisone acetate USP in a hydrogenated cocoglyceride base. Hydrocortisone acetate is a corticosteroid.
Chemically, hydrocortisone acetate is pregn-4-ene-3, 20 dione, 21- (acetyloxy)-11, 17-dihydroxy-, (11β)- with the following structural formula:Chemical Structure
In normal subjects, about 26 percent of hydrocortisone acetate is absorbed when the hydrocortisone acetate suppository is applied to the rectum. Absorption of hydrocortisone acetate may vary across abraded or inflamed surfaces.
Topical steroids are primarily effective because of their anti-inflammatory, antipruritic and vasoconstrictive action.
Hydrocortisone Acetate Indications and Usage
For use in inflamed hemorrhoids, post irradiation (factitial) proctitis, as an adjunct in the treatment of chronic ulcerative colitis, cryptitis, other inflammatory conditions of the anorectum, and pruritus ani.
Hydrocortisone acetate suppositories are contraindicated in those patients with a history of hypersensitivity to any of the components.
Do not use unless adequate proctologic examination is made.
If irritation develops, the product should be discontinued and appropriate therapy instituted.
In the presence of an infection, the use of an appropriate antifungal or antibacterial agent should be instituted. If a favorable response does not occur promptly, the corticosteroid should be discontinued until the infection has been adequately controlled.
No long-term studies in animals have been performed to evaluate the carcinogenic potential of corticosteroid suppositories.
In laboratory animals, topical steroids have been associated with an increase in the incidence of fetal abnormalities when gestating females have been exposed to rather low dosage levels. There are no adequate and well-controlled studies in pregnant women.
It is not known whether this drug is excreted in human milk.
Until adequate studies in pregnant or lactating women have been conducted, this drug should be used during pregnancy or by nursing mothers only when clearly needed and when the potential benefits outweigh the potential risks.
The following local adverse reactions have been reported with corticosteroid suppositories:
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Drug abuse and dependence have not been reported in patients treated with hydrocortisone acetate suppositories.
If signs and symptoms of systemic overdosage occur, discontinue use.
One suppository in the rectum morning and night for two weeks, in nonspecific proctitis. In more severe cases, one suppository three times daily; or two suppositories twice daily. In factitial proctitis, recommended therapy is six to eight weeks or less, according to response.
Hydrocortisone acetate suppositories are easy to open, color coded and available in cartons of:
Store at controlled room temperature 15° to 30°C (59° to 86°F). Protect from freezing.
Minneapolis, MN 55427
PRINCIPAL DISPLAY PANEL — 12 Packet Box Label
CommUnityCare Federally Qualified Health Centers
SUPP.25MG # 12
USE AS DIRECTED BY DOCTOR.
Hydrocortisone Supp. 25 mg #12 NDC 76413-132-12
Federal law prohibits the transfer of this drug to any other person than the patient for whom prescribed.
| HYDROCORTISONE ACETATE |
hydrocortisone acetate suppository
|Labeler — Central Texas Community Health Centers (079674019)|
|Central Texas Community Health Centers||079674019||REPACK (76413-132), RELABEL (76413-132)|
Revised: 04/2016 Central Texas Community Health Centers
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