Repro Flashcards

1
Q

Leuprolide

MOA

A

GnRH analog
Pulsatile - agonist
Continuous - antagonist

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2
Q

Leuprolide

Clinical use

A

Infertility (pulsatile)
Prostate cancer, uterine fibroids (continuous)
Precocious puberty (continuous)

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3
Q

Estrogens (Ethinyl estradiol, DES, mestranol)

Clinical use

A

Binds estrogen receptors.

For hypogonadism, ovarial failure, menses abnormalities, HRT.

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4
Q

Estrogens

Toxicity

A

Inc. risk Endometrial cancer.
Bleeding in postmenopause.
CI in ER-positive breast cancer, hx of DVT.

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5
Q

Clomiphene

[MOA, clinical use]

A

SERM – Estrogen receptor antagonist at hypothalamus.
Prevents feedback inhibition – inc. LH/FSH – ovulation.
For infertility (anovulation).

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6
Q

Tamoxifen

[MOA, clinical use, toxicity]

A

SERM: Antagonist at breast; agonist at bone, uterus.
Treat and prevent recurrence of ER/PR-positive breast cancer.
Tox: inc. risk of thromboembolism, endometrial cancer.

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7
Q

Raloxifene

[MOA, clinical use]

A

SERM: Antagonist at breast, uterus; agonist at bone.
Treat osteoporosis.
Inc. risk of thromboembolism.

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8
Q

Hormone replacement therapy.
For what?
Estrogen? Progesterone?

A

For menopausal sx, osteoporosis.

Unopposed estrogen inc. risk of endometrial cancer – add progesterone (estrogen + progesterone).

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9
Q

Progestins

[MOA, clinical use]

A

Bind progesterone receptors. Used in OCPs.
Dec. growth and inc. endometrial vascularization.
For endometrial cancer, abnormal uterine bleeding.

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10
Q

Oral contraception

MOA

A

Estrogen + progestin.
Inhibit LH/FSH – no estrogen surge – no LH surge – no ovulation.
> Progestins: thick cervical mucus, limits sperm access to uterus; inhibit endometrial proliferation, so harder to implant.

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11
Q

Oral contraception

Contraindications

A

Smokers > 35 y.o
Hx of thromboembolism, stoke
Hx. of estrogen-dependent tumor

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12
Q

Terbutaline, Ritodrine

Clinical use

A

B2-agonists
Relax the uterus.
To dec. contraction frequency in labor.

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13
Q

Testosterone

Clinical use

A

Androgen receptor agonist.

For hypogonadism; to develop secondary sex chars.

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14
Q

Testosterone

Toxicity

A

Masculinization in females.
Gonadal atrophy in males (inhibits LH release) – dec. intratesticular testosterone.
Premature closure of epiphyseal plates.

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15
Q

Finasteride

[MOA, use]

A

Antiandrogen; 5a-reductase inhibitor (testosterone –> DHT).

For BPH, male-pattern baldness.

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16
Q

Flutamide

[MOA, use]

A

Antiandrogen; Nonsteroidal competitive androgen receptor inhibitor.
For prostate CA.

17
Q

Ketoconazole

[MOA, use, SE]

A

Antiandrogen.
Inhibits 17,20-desmolase (cholesterol – androgen) – Inhibits steroid synthesis.
For polycystic ovarian syndrome – reduce androgenic sx.
SE: gynecomastia, amenorrhea

18
Q

Spironolactone

[MOA, use, SE]

A

Antiandrogen.
Inhibits steroid binding, 17a-hydroxylase, 17,20-desmolase.
For polycystic ovarian syndrome.
SE: gynecomastia, amenorrhea

19
Q

Tamsulosin

[MOA, use]

A

a1-antagonist (alpha1A,D receptors in prostate).
Inhibit smooth muscle contraction, for BPH.
Treat BPH

20
Q

Sildenafil, Vardenafil, Tadalafil

[MOA, clinical use]

A

Inhibit PDE-5 – inc. cGMP – smooth muscle relaxation in corpus cavernosum, inc. blood flow – penile erection.
For erectile dysfunction.

21
Q

Sildenafil, Vardenafil, Tadalafil

Toxicity

A

Life-threatening Hypotension in pts taking nitrates.

Headache, heartburn

22
Q

Anastrozole/Exemestane

[MOA, use]

A

Aromatase inhibitors.
Used in postmenopausal women w/ ER-positive breast cancer.
*Source of estrogen after menopause becomes peripheral conversion of androgens.

23
Q

Danazol

[MOA, use]

A

> Partial agonist at androgen receptors – induces a state of pseudomenopause by suppressing ovarian fxn and inhibits FSH/LH secretion, causing endometrial atrophy.
For endometriosis, hereditary angioedema.

24
Q

Mifepristone (RU-486)

[MOA, use]

A

Competitive inhibitor of pregestins at progesterone receptor.
Termination of pregnancy.
*Administer w/ misoprostol (PGE1)