Fludrocortisone: Difference between revisions
No edit summary |
m (Bot: Automated text replacement (-{{SIB}} + & -{{EJ}} + & -{{EH}} + & -{{Editor Join}} + & -{{Editor Help}} +)) |
||
(One intermediate revision by the same user not shown) | |||
Line 20: | Line 20: | ||
{{SI}} | {{SI}} | ||
'''Fludrocortisone''' is a synthetic [[corticosteroid]] with moderate [[glucocorticoid]] potency and much greater [[mineralocorticoid]] potency. It is used primarily to replace the missing hormone [[aldosterone]] in various forms of [[adrenal insufficiency]] such as [[Addison's disease]] and the classic salt wasting (21-hydroxylase deficiency) form of [[congenital adrenal hyperplasia]]. It is occasionally used to treat [[orthostatic hypotension]] as well. | '''Fludrocortisone''' is a synthetic [[corticosteroid]] with moderate [[glucocorticoid]] potency and much greater [[mineralocorticoid]] potency. It is used primarily to replace the missing hormone [[aldosterone]] in various forms of [[adrenal insufficiency]] such as [[Addison's disease]] and the classic salt wasting (21-hydroxylase deficiency) form of [[congenital adrenal hyperplasia]]. It is occasionally used to treat [[orthostatic hypotension]] as well. | ||
Line 27: | Line 27: | ||
Chemically, its structure is identical to cortisone except for the substitution of F in place of one hydrogen. F is a good [[bioisostere]] for hydrogen because it is similar in size. The major difference is in its [[electronegativity]]. | Chemically, its structure is identical to cortisone except for the substitution of F in place of one hydrogen. F is a good [[bioisostere]] for hydrogen because it is similar in size. The major difference is in its [[electronegativity]]. | ||
[[Category:Mineralocorticoids]] | [[Category:Mineralocorticoids]] | ||
[[Category:Organofluorides]] | [[Category:Organofluorides]] |
Latest revision as of 02:46, 9 August 2012
Clinical data | |
---|---|
Pregnancy category |
|
Routes of administration | oral |
ATC code | |
Pharmacokinetic data | |
Protein binding | High |
Metabolism | Hepatic |
Elimination half-life | 3.5 hours |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
DrugBank | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C21H29FO5 |
Molar mass | 380.45 g/mol |
WikiDoc Resources for Fludrocortisone |
Articles |
---|
Most recent articles on Fludrocortisone Most cited articles on Fludrocortisone |
Media |
Powerpoint slides on Fludrocortisone |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Fludrocortisone at Clinical Trials.gov Trial results on Fludrocortisone Clinical Trials on Fludrocortisone at Google
|
Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Fludrocortisone NICE Guidance on Fludrocortisone
|
Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Fludrocortisone Discussion groups on Fludrocortisone Patient Handouts on Fludrocortisone Directions to Hospitals Treating Fludrocortisone Risk calculators and risk factors for Fludrocortisone
|
Healthcare Provider Resources |
Causes & Risk Factors for Fludrocortisone |
Continuing Medical Education (CME) |
International |
|
Business |
Experimental / Informatics |
Fludrocortisone is a synthetic corticosteroid with moderate glucocorticoid potency and much greater mineralocorticoid potency. It is used primarily to replace the missing hormone aldosterone in various forms of adrenal insufficiency such as Addison's disease and the classic salt wasting (21-hydroxylase deficiency) form of congenital adrenal hyperplasia. It is occasionally used to treat orthostatic hypotension as well.
The brand name in the U.S. is Florinef. It is available in 0.1 mg tablets. Typical daily doses for mineralocorticoid replacement are between 0.05 mg - 0.2 mg. Renin plasma, sodium, and potassium is checked through blood tests in order to verify that the correct dosage is reached.
Chemically, its structure is identical to cortisone except for the substitution of F in place of one hydrogen. F is a good bioisostere for hydrogen because it is similar in size. The major difference is in its electronegativity.
Template:Corticosteroids Template:Corticosteroids for systemic use
- Pages with script errors
- E number from Wikidata
- ECHA InfoCard ID from Wikidata
- Articles without EBI source
- Chemical pages without ChemSpiderID
- Articles without KEGG source
- Articles without InChI source
- Articles without UNII source
- Drugs with no legal status
- Articles containing unverified chemical infoboxes
- Mineralocorticoids
- Organofluorides