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18 Cards in this Set

  • Front
  • Back
finasteride
- antiandrogen, 5-alpha reductase inhibitor (converts testosterone to DHT)
- useful in BPH, promotes hair growth
flutamide
- competitive inhibitor of androgens at the testosterone receptor
-used in prostate carcinoma
ketoconazole
- an antifungal that inhibits steroid synthesis
- polycystic ovarian syndrome
- side effect- gynecomastia, amenorrhea
spironolactone
- inhibits steroid binding
- side effects include gyencomastia & amenorrhea
leuprolide
- 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
sildafenil, vardenafil
- 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
mifepristone (RU-486)
- 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
oral contraception
- prevent estrogen surge so LH surge doesn't occur, no ovulation
hormone replacement therapy
- used for relief/prevention of menopause symptoms and osteoporosis
- unopposed estrogen therapy increase risk for endometrial cancer
dinoprostone
-PGE2 analog causing cervical dilation and uterine contraction
- used to induce labor
ritodrine/terbutaline
- beta 2 agonists that relax the uterus
- used to reduce premature uterine contractions
anastrozole, exemestane
-aromatase inhibitors (it converts testosterone & DHT to estrogen)
- used in postmenopausal women with breast cancer
testosterone
- 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
estrogens (ethinyl estradiol, DES, mestranol)
- 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
progestins
- 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
clomiphene
- 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
tamoxifen
- estrogen antagonist on breast tissue
-used to prevent and treat recurrence of ER+ breast cancer
raloxifene
- estrogen agonist on bone, reduces resorption of bone
-used to treat osteoporosis (estrogen inhibits osteoclasts and stimulates osteoblasts)