Hormones Pharm part II, Linger Flashcards

1
Q

best way to Tx mild side effects of birth control pills

A

change pill formulation

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2
Q

best way to Tx moderate side effects of BCP

A

discontinue Tx

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3
Q

what are the moderate side effects BCP

A
break through bleeding
weight gain
increased skin pigmentation
acne
hirsutism
vaginal ingections
amenorrhea
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4
Q

what are the serious side effects to BCPs

A

vascular disorders: DVT, MI, CVD
GI disorders: cholestatic jaundice, cholestasis, increased hepatic adenomas
depression
Cancer

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5
Q

contraindications to E containing BCPs

A

smokers >35 y.o, HTN, CAD, CVD, DM with end organ damage, migraine HA, vaginal bleeding of unknown cause
adolescent where epiphyseal closure has not yet happened

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6
Q

P only BCP contraindicated

A

unDx vaginal bleeding, benign or malignant liver disease, known or suspected breast CA

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7
Q

BCP used with caution in

A

liver disease, asthma, eczema, migrain, DM, HTN, optic neuritis, retrobulbular neuritis or convulsive disorders

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8
Q

what BCP used in woman with fibroids

A

P only since E increase fibroid growth

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9
Q

non contraceptive benefits of E and P BCP

A

reduced risk epithelial ovarian and endometrial CA
lower incidence ectopic pregnancy and benign breast disease
reduction in dysfunctional uterine bleeding and dysmenorrhea
improvement in premenstrual Sx

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10
Q

MOA tamoxifen and toremifene

A

competitive partial agonist inhibitors of estradiol at E Receptro

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11
Q

clinical use of tamoxifen

A

used to Tx Breast CA and chemoprevention of breast CA in high risk patients

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12
Q

agonist effects of tamoxifen

A

lower chance fracture
reducs in risk atherosclerosis
increase thromboembolic disease
increase risk endometrial CA

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13
Q

side effect tamoxifen

A

hot flashes

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14
Q

MOA taloxifene

A

agonist on lipids and bone, antagonis on endometrium and breast

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15
Q

raloxifene is used for prevention of what

A

postmenopausal osteoporosis and chemoprevention of breast CA in at risk individuals

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16
Q

advserse effects raloxifene

A

hot flashes, DVT, leg cramps

17
Q

MOA fulvestrant

A

binds E R and inhibit dimerization while increasing degradation

18
Q

what is used once someone has become resistant to tamoxifen

A

fulvestrant

19
Q

adverse effects fulvestrant

A

hot flashes, GI Sx, HA, back pain and pharyngitis

20
Q

MOA clomiphene

A

weak E, acts as competitive partial agonist inhibior of endogenous E

21
Q

clomiphene is used for what

A

ovulation inducing agent

22
Q

adverse effects clomiphene

A

ovarian hyperstimulation, increased incidence multiple births, ovarian cysts, hot flashes, blurred vision

23
Q

MOA mifepristone

A

acts on P R antagonist and antagonizes glucocorticoid R

24
Q

major use of mifepristone

A

terminate early pregnancies

25
mifepristone is usually combine with what to terminate pregnancy
misoprostol, synthetic PG E1
26
major adverse effects to mifepristone
nausea, vomiting, diarrhea, pelvic or abdominal pain and prolonged vaginal bleeding
27
What is used for Tx endometriosis and fibrocystic disease of breast
danazol
28
danazol is contraindicated in what patients
pregnant ones
29
MOA aromatase inhibitors
inhbiit aromatase which converts androstenedione and testosterone to the E: estron and estradiol
30
aromatase inhibitors are only used in postmenopausal women why
use can lead to profound E deprivation | may reactivate ovarian function in premenopausal women
31
how can aromatase inhibitor increase ovulation
decrease E so increase LH and FSH from removal of negative feedback =ovulation
32
most effective drug at lowering incidence of hot flashes, endometrial CA, DVT
aromatase inhibitors
33
MOA clomiphene
partial agonist E R but binds for longer duration impairing E negative feedback increasing GnRH pulsatile signals to increase FSH and LH for ovulation
34
clincal use clomiphene
stimulate obulation in women with oligomenorrhea and amenorrhea and ovulatory dysfunction
35
adverse effects clomiphene
hot flashes ovarian enlargement increased incidence multiple pregnancies