Pharm endocrine (Reproduction) drugs Flashcards

1
Q

Estrogens

A
  • Sythetics undergo 1st pass metab - turn into naturally occuring steroid
  • MOA:
  • Activation of estrogen receptors - Transcription rates upreg
  • Considerations:
  • Women w/uterus give w/progestin to prevent endometrial cancer
  • Clinical applications:
  • Contraception - synthetics high bioavail
  • Hormone therapy: post menopausal (small increase risk of breast cancer & CV events)
  • Premature ovarian failure
  • Hypogonadism in young female (IM admin)
  • Prevention of bone loss in osteoporsis
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2
Q

Estrogens Effects

A
  • Mestranol - prodrug converted to ethinyl estradiol
  • Adverse effects:
  • Minor - breakthrough bleeding, nausea, breast tenderness
  • Major - Thromboembolism, Gallbladder disease, hypertriglycerdemia, depression
  • In postmeno women = breast cancer & endometrial hyperplasia
  • Drug interactions:
  • Combo with **CYP 450 inducer can lead to BREAKthrough bleeding & reduced contraceptive **
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3
Q

Oral contraceptives & antibiotics

A
  • Rifampin: used to treat TB
  • Stong inducer of CYP 3A4 & 2C9
  • ONLY antibiotic proven to interact with OCs
  • Other antibiotics linked to decreased effectiveness ; Amoxicillin, ampicillin, tetracycline
  • Combo contraceptives include doses 15-50 of Ethinyl estradiol to REDUCE thromboemolism
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4
Q

Diethylstilbestrol

A
  • Approved for gonorrhea, menopause, atrophic vaginitis, postpartum lactation supression
  • Carcinogenic:
  • DES daughters 40x more likely to have vaginal clear cell carcinoma, Tumors on repro tract and breast
  • _Teratogenic: _
  • Malformations in repro tract of users (Hypospadia)
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5
Q

Progestins

A
  • MOA: Activate progesterone receptors
  • Clinical applications:
  • Contraception (with or without estrogen)
  • Treat hormone def
  • Assisted repro tech to promote & maintain preg
  • Control of dysfunctional uterine bleeding
  • Dysmenorrhea (painful periods) & endometriosis
  • Adverse effects:
  • Weight gain
  • Decrease in bone mineral density W/high doses
  • May increase BP & decrease HDL
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6
Q

Progesterone & synthetics

A
  • Progesterone: not used due to rapid metab
  • Synthetic:
  • Derived from 19-nortestosterone & produce androgenix activity - oral contraceptive
  • 3 generations & 3rd highest risk for Blood clots
  • 4th generation = 17-a spirolactone = Drospirenone
  • Medroxyprogesterone acetate (depo-provera) - injectable contraceptive (3months)
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7
Q

Progestin (POP)

A
  • Progestin only pills
  • Low dose:
  • Implants - Norplant or Mirena
  • Inhibit ovulation in 50%
  • Thicking cervical mucus - Reduce sperm
  • Medium dose:
  • Implant - Nexplanon
  • Some follicular development, BUT inhibit ovulation in 99%
  • Similar mucus changes
  • High dose:
  • Implant - depo-provera
  • COMPLETE inhibit follicular development & ovulation
  • Similar mucus changes
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8
Q

SERM (Tamoxifen)

A
  • Selective estrogen receptor mods
  • MOA:
  • Estrogen antagonist actions in breast tissue & CNS
  • Estrogen agonist effects in liver/bone
  • Clinical use:
  • Prevention & adjuvant treatment of hormone responsive breast cancer
  • Increase bone density in postmeno
  • Adverse effects:
  • Hot flashes, thromboemolism, endometrial hyperplasia
  • Increase endometrial cancer
  • Toremifene SIMILAR
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9
Q

Other SERMs (-fene)

A
  • Raloxifene: Antagonist in breast & CNS metab & Agonist in liver
  • Clinical uses: Approved for osteoporosis & prevention of breast cancer In SOME post menopausal
  • Clomiphene: Antagonist effect on Pit increases gonadotropin secretion
  • Clinical uses: ovulation induction
  • Ormeloxifene: non-hormonal & steroidal oral contraceptive
  • MOA: agonist bone, antagonist uterus/breast
  • Adverse effects: uterine prolaspe or urinary incontinence
  • Lasofoxifene: Agonist bones, Antagonist breast/uterus
  • NOT approved by FDA due to osteoporosis - used in EU
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10
Q

SERD (Fulvestrant)

A
  • Selective estrogen down reg (SERD)
  • Monthly IM injection
  • MOA
  • Estrogen receptor antagonist (-) in all tissues
  • Clinical use:
  • 2nd line treatment for hormone-responsive breast cancer that is resistant to 1st line antiestrogen therapy
  • Adverse effects:
  • Hot flushes, headache, nausea, asthenia (weakness)
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11
Q

Aromatase Inhibitors

A
  • Large amount of estrogen made locally in endrometric cells - Estradiol also occurs in tissues
  • Ex. Adipose tissue, skin fibroblasts
  • GnRH agonists DO NOT inhibit peripheral estrogen production
  • Aromatase inhib CAN
  • MOA:
  • Block aromatase enzyme -
  • competitive inhbition (Anastrozole & letrozole)
  • Covalently bind (Exmestane, formestane)
  • Clinical: adjuvant treatment of hormone breast cancer
  • Adverse effects: Muscloskeletal disorders, dyspnea, bone pain
  • Serious = Osteoporotic fractures, profuse vaginal bleeding
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12
Q

Danazol

A
  • MOA:
  • Weak cyto P450 inhibitor & partial agonist of progestin/androgen receptors
  • Synthetic derive from 17-ethinyltesteroine (4th generation)
  • Results = Decrease FSH & LH
  • Clinical uses:
  • Fibrocystic breast disease
  • Endometrosis: induces anovulation, amenorrhea, endometrial atrophy (Lowered LH/FSH)
  • Adverse effects: Acne, hirsutism, weight gain, decreased breast size
  • Drug interactions:
  • CYP450 drug interactions
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13
Q

Antiprogestin - (Mifepristone)

A
  • MOA: progestin & glucocorticoid receptor antagonist (-)
  • Clinical uses: combo w/prostaglandin (misoprostaol) for abortion
  • Adverse effects:
  • GI
  • Vaginal bleeding
  • Atypical infection
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14
Q

Testosterone (androgens)

A
  • MOA
  • Androgen receptor agonist
  • Clinical use
  • Male Hypogonadism
  • Wasting syndrome - helps gain weight
  • Adverse effets
  • Virilization in females (Deep voice)
  • High doses cause gynecomastia in men
  • Testicular shrinkage & infertility
  • Oral = Fluoxymesterone, methyltesto
  • Esters = Testoterone cypionate (long lasting)
  • Anabolic = oxandrolone, nandrolone decanoate - (liver toxicities)
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15
Q

Antiandrogens (Finasteride)

A
  • MOA: Inhibition of 5a reductase enzyme converts testo to dihydrotesto
  • Clinical:
  • Benign prostatic hyperplasia
  • Male pattern hair loss
  • Adverse effects:
  • RARE: Gynecomastia, impotence
  • Dutasteride similar
  • Propecia
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16
Q

Flutamide

A
  • Androgen receptor antagonist
  • MOA: comp inhibition of androgen receptor
  • Clinical
  • Advanced prostate cancer
  • Adverse effects:
  • Gyncomastia, hot flashes, impotence, heptoxicity
  • Bicalutamide & Nilutamide - similar BUT lower hepatotoxicity
17
Q

Spironolactone

A
  • MOA:
  • mineralcorticoid receptor antagonist (-)
  • Androgen receptor antagonist (-)
  • Clinical:
  • K+ sparing diuretic
  • Other uses: Hirsitism, acne, Hypokalemia, primary aldosteronism
  • Adverse effects:
  • Gynecomastia, dyspepsia (impaired digestion), lethargy, rash
18
Q

Menorrhagia

A
  • Excessive or prolonged bleeding
  • Could be caused by uterine leiomyoma (benign tumors)
  • Pressure sense in lower ab
  • Treat tumor w/GnRH agonists = reduction in uterine size or Levonorgestrel-intrauterine device = reduction in uterine volume & bleeding
  • Pharmacotherapy:
  • Combined oral contraceptives
  • NSAIDs
  • Tranexamic acid - antifibrinolytic agent reversible blockage of lysine binding site on plasmonogen mol (no Coag)
19
Q

Endometriosis

A
  • Symptoms:
  • Recurrance of pain
  • Dysmenorrhea, dyspareunia, dysuria, pain during defecation, infertility
  • Pharmcotherapy:
  • Drugs to supress ovarian function & endometrial growth
  • Progestins - oral contraceptives
  • GnRH agonists
  • Danazol
  • Other treatment:
  • Surgical ablation & excision
20
Q

Polycystic ovarian Syndrome

A
  • Symptoms:
  • Mestrual irreg
  • Amernorrhea
  • Hirsutism
  • Acne
  • infertility
  • Mild obesity
  • Thicked dark skin in axillae, nape of neck
  • Phramocotherapy - combined oral contraceptives
  • Used along with antiandrogens for nomalizing dysfunctional uterine bleeding & Treat hisutism in 6months (spironolactone, GnRH agonists, Flutamide)