Cyproterone chemical structure
Find information on thousands of medical conditions and prescription drugs.

Cyproterone

Cyproterone acetate (Androcur®, Cyprostat®, Cyproteron®, Procur®, Cyprone®, Cyprohexal®, Ciproterona®, Cyproteronum®, Neoproxil®) is an antiandrogen, i.e., it suppresses the actions of testosterone (and its metabolite dihydrotestosterone) on tissues. It acts by blocking androgen receptors which prevents dihydrotestosterone from binding to them and suppresses luteinizing hormone (which in turn reduces testosterone levels). more...

Home
Diseases
Medicines
A
B
C
Cabergoline
Caduet
Cafergot
Caffeine
Calan
Calciparine
Calcitonin
Calcitriol
Calcium folinate
Campath
Camptosar
Camptosar
Cancidas
Candesartan
Cannabinol
Capecitabine
Capoten
Captohexal
Captopril
Carbachol
Carbadox
Carbamazepine
Carbatrol
Carbenicillin
Carbidopa
Carbimazole
Carboplatin
Cardinorm
Cardiolite
Cardizem
Cardura
Carfentanil
Carisoprodol
Carnitine
Carvedilol
Casodex
Cataflam
Catapres
Cathine
Cathinone
Caverject
Ceclor
Cefacetrile
Cefaclor
Cefaclor
Cefadroxil
Cefazolin
Cefepime
Cefixime
Cefotan
Cefotaxime
Cefotetan
Cefpodoxime
Cefprozil
Ceftazidime
Ceftriaxone
Ceftriaxone
Cefuroxime
Cefuroxime
Cefzil
Celebrex
Celexa
Cellcept
Cephalexin
Cerebyx
Cerivastatin
Cerumenex
Cetirizine
Cetrimide
Chenodeoxycholic acid
Chloralose
Chlorambucil
Chloramphenicol
Chlordiazepoxide
Chlorhexidine
Chloropyramine
Chloroquine
Chloroxylenol
Chlorphenamine
Chlorpromazine
Chlorpropamide
Chlorprothixene
Chlortalidone
Chlortetracycline
Cholac
Cholybar
Choriogonadotropin alfa
Chorionic gonadotropin
Chymotrypsin
Cialis
Ciclopirox
Cicloral
Ciclosporin
Cidofovir
Ciglitazone
Cilastatin
Cilostazol
Cimehexal
Cimetidine
Cinchophen
Cinnarizine
Cipro
Ciprofloxacin
Cisapride
Cisplatin
Citalopram
Citicoline
Cladribine
Clamoxyquine
Clarinex
Clarithromycin
Claritin
Clavulanic acid
Clemastine
Clenbuterol
Climara
Clindamycin
Clioquinol
Clobazam
Clobetasol
Clofazimine
Clomhexal
Clomid
Clomifene
Clomipramine
Clonazepam
Clonidine
Clopidogrel
Clotrimazole
Cloxacillin
Clozapine
Clozaril
Cocarboxylase
Cogentin
Colistin
Colyte
Combivent
Commit
Compazine
Concerta
Copaxone
Cordarone
Coreg
Corgard
Corticotropin
Cortisone
Cotinine
Cotrim
Coumadin
Cozaar
Crestor
Crospovidone
Cuprimine
Cyanocobalamin
Cyclessa
Cyclizine
Cyclobenzaprine
Cyclopentolate
Cyclophosphamide
Cyclopropane
Cylert
Cyproterone
Cystagon
Cysteine
Cytarabine
Cytotec
Cytovene
Isotretinoin
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z

Its main indications are prostate cancer, benign prostatic hyperplasia, priapism, hypersexuality and other conditions in which androgen action maintains the disease process. Due to its anti-androgen effect, it can also be used to treat hirsutism, and is a common component in hormone therapy for male-to-female transgendered people.

Until the development of leuprolide, cyproterone was one of the few drugs used to treat precocious puberty. It was also used in animal experimentation to investigate the actions of androgens in fetal sexual differentiation.

In addition, its acetate form (cyproterone acetate) has weak progestational activity (e.g., it acts like progesterone). As part of some contraceptive pills (Diane®) it decreases acne and hirsutism (male-pattern hair growth).

Side-effects in men include gynecomastia (breast growth) and galactorrhea (milk outflow). Erectile dysfunction is a direct result of its mode of action.

Read more at Wikipedia.org


[List your site here Free!]


Evaluation and management of hirsutism in women - Tips from Other Journals - Author Abstract
From American Family Physician, 1/15/04 by Anne D. Walling

Hirsutism affects between 5 to 15 percent of adult women surveyed for the condition. The excessive growth of coarse hair in a male-like pattern can cause significant distress and have multiple negative consequences for patients. Hyperandrogenism usually causes hirsutism. A review by Azziz stresses the need for a systematic evaluation of the patient and use of combination therapy.

The first step in the evaluation of hirsutism is confirmation of excessive coarse (terminal) hairs in a male-like pattern, because many patients who complain of excessive hair growth do not have true hirsutism. Several scoring systems have been developed, but they must be adapted to the ethnic and cultural group to which each patient belongs, because body hair is regarded very differently by different cultures.

The second step involves the identification of the disorders (e.g., adrenal hyperplasia, diabetes mellitus, thyroid dysfunction, ovulatory conditions) that could contribute to the etiology or complicate the management of hirsutism. The most common causes of hirsutism are androgenic. Approximately 70 to 80 percent of women with androgen excess have hirsutism. The most common cause of androgen excess is polycystic ovary syndrome (PCOS). Rarer androgenic causes include the insulin-resistant acanthosis nigricans syndrome, some forms of adrenal hyperplasia, and ovarian or adrenal androgen-secreting tumors. Approximately 5 to 15 percent of hirsutism cases are idiopathic (i.e., an underlying cause cannot be identified). Some of these women are believed to have enzyme overactivity in the hair follicles, causing hirsutism in spite of normal circulating hormone levels.

Establishing the etiology of hirsutism depends on a thorough medical and menstrual history plus a physical examination, followed by laboratory and other diagnostic tests targeting the most probable cause for the individual patient. Appropriate tests may include thyroid function; basal 17-hydroxyprogesterone level during the follicular phase of menstruation to exclude nonclassic adrenal hyperplasia; blood glucose and insulin levels; and measures of circulating androgen levels (total and free testosterone and dehydroepiandrosterone sulfate).

Pharmacologic treatment is directed at the underlying cause of hirsutism, with special attention given to associated risk factors. More than one half of women with PCOS are at significant risk of insulin resistance and diabetes. Suppression of ovarian androgens usually is obtained through the use of combined oral contraceptives. Use of estrogens alone (1.25 mg of conjugated equine estrogens daily) in appropriate women has been recommended. Oral contraceptives may be combined with long-acting gonadotropin-releasing hormone (Gn-RH) analogs, such as Lupron Depot in a dosage of 3.75 mg per month, but this approach generally requires two to three cycles for effect. Insulin resistance may respond to weight loss or therapy with metformin or troglitazone, but the effect on hirsutism may be modest. The most effective treatments combine androgen suppression with peripheral androgen blockade. Androgen-receptor blockers include spironolactone, flutamide, finasteride, and cyproterone acetate. These drugs have teratogenic potential and require secure contraception.

In addition to medical treatments, most women with hirsutism seek local treatments to minimize the appearance of unwanted hair. Shaving does not increase hair growth. Depilating agents can cause chronic skin irritation. Mechanical hair removal by waxing or plucking is discouraged because of the risk of trauma, ingrown hairs, and folliculitis. Electrolysis and laser therapy can be successful but have unwanted side effects, such as blistering and pigmentation changes. Eflornithine hydrochloride 13.9 percent cream is approved by the U.S. Food and Drug Administration for treatment of unwanted facial hair. This agent slows and miniaturizes hair growth but appears to require continuous application. It has been associated with improvement in 60 percent of cases in initial studies and requires at least eight weeks of treatment for effectiveness.

Azziz R. The evaluation and management of hirsutism. Obstet Gynecol May 2003;101:995-1007.

COPYRIGHT 2004 American Academy of Family Physicians
COPYRIGHT 2004 Gale Group

Return to Cyproterone
Home Contact Resources Exchange Links ebay