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18 Cards in this Set
- Front
- Back
finasteride
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- antiandrogen, 5-alpha reductase inhibitor (converts testosterone to DHT)
- useful in BPH, promotes hair growth |
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flutamide
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- competitive inhibitor of androgens at the testosterone receptor
-used in prostate carcinoma |
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ketoconazole
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- an antifungal that inhibits steroid synthesis
- polycystic ovarian syndrome - side effect- gynecomastia, amenorrhea |
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spironolactone
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- inhibits steroid binding
- side effects include gyencomastia & amenorrhea |
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leuprolide
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- GnRH analog with agonist properties when used in a pulsatile fashion and ANTAGonist properties when used continuously
- used for infertility(pulse it), prostate cancer (continuous, use w/ flutamide), uterine fibroids tox: nausea, vomiting, antiandrogen |
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sildafenil, vardenafil
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- inhibit cGMP phosphodiesterase causing increased cGMP, smooth muscle relaxtion in corpus cavernosum, increase blood flow and penile erection
- treat erectile dysfunction - tox: headache, flushing, dyspepsia, **risk of life threatening hypoTN in pts taking nitrates**, impaired blue-green color vision |
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mifepristone (RU-486)
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- morning after pill
- competitive inhibitor of progestins at progesterone receptors - used for termination of pregnancy. given with misoprostol (PGE1 analog) tox: heavy bleeding, GI effects, abdominal pain |
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oral contraception
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- prevent estrogen surge so LH surge doesn't occur, no ovulation
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hormone replacement therapy
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- used for relief/prevention of menopause symptoms and osteoporosis
- unopposed estrogen therapy increase risk for endometrial cancer |
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dinoprostone
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-PGE2 analog causing cervical dilation and uterine contraction
- used to induce labor |
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ritodrine/terbutaline
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- beta 2 agonists that relax the uterus
- used to reduce premature uterine contractions |
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anastrozole, exemestane
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-aromatase inhibitors (it converts testosterone & DHT to estrogen)
- used in postmenopausal women with breast cancer |
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testosterone
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- agonist at androgen receptors
- treat hypogonadism and promote development of secondary sex characteristics, treat ER+ breast cancer (exemestane) tox: masculinization in females, inhibit leydig cells thereby reducing inratesticular testosterone, gonadal atrophy, premature closure of epiphyseal plates. increase LDL, decrease HDL |
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estrogens (ethinyl estradiol, DES, mestranol)
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- binds estrogen receptors
- used for ovarian failure, menstrual abnormalities, HRT, use in men with androgen dependent prostate cancer tox: increase risk of endometrial cancer, bleeding in postmenopausal women, CLEAR CELL ADENOCARCINOMA of vagina in females exposed to DES in utero |
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progestins
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- bind progesterone receptors, reduce growth and increase vascularization of the endometrium
- used in oral contraceptives and in the tx of endometrial cancer, abnormal uterine bleeding |
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clomiphene
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- estrogen partial agonist in pituitary, prevents normal feedback inhibition and increase release of LH, FSH to stimulate ovualtion
- used to treat infertility & PCOS. may cause multiple simultaneous pregnancies |
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tamoxifen
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- estrogen antagonist on breast tissue
-used to prevent and treat recurrence of ER+ breast cancer |
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raloxifene
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- estrogen agonist on bone, reduces resorption of bone
-used to treat osteoporosis (estrogen inhibits osteoclasts and stimulates osteoblasts) |