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Diprolene Af

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* Based on 2 reviews from across the web.
Wikipedia

Betamethasone is a steroid medication. It is used for a number of diseases including rheumatic disorders such as rheumatoid arthritis and systemic lupus erythematosus, skin diseases such as dermatitis and psoriasis, allergic conditions such as asthma and angioedema, preterm labor to speed the development of the baby, Crohn disease, cancers such as leukemia, and along with fludrocortisone for adrenocortical insufficiency, among others. It can be taken by mouth, injected into a muscle, or applied as a cream. When given by injection, anti-inflammatory effects begin in around two hours and last for seven days.

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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 kpbeatty in drugs.com on March 30, 2009 @ 12:00 am

Diprolene AF (betamethasone) for Atopic Dermatitis: Rapid improvement in red areas on neck, chest and elbows.

Druginformer Identified Side Effects: Sinusitis, Adrenal insufficiency, Skin atrophy, Adrenal suppression

Posted By Anonymous in askapatient.com on March 17, 2007 @ 12:00 am

Side Effects: Skin atrophy, severe adrenal suppression, chronic infections due to immune compromise, adrenal insufficiency upon discontinuation Use this with great caution, only in the a.m....


* 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.