Drugs Flashcards

1
Q

What is the MOA of minoxidil?

What is it used for? (2)

A

Minoxidil

  • Direct arteriolar vasodilator
  • Male pattern baldness, severe HTN
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2
Q

What is the MOA of sildenafil?

Clinical use (2)

Side effects (5)

A

Sildenafil

  • PDE-5 inhibitor -> increased cGMP -> vasodilation
  • Treats erectile dysfunction, pulmonary HTN
  • Hot & sweaty, headache, hypotension, heartburn, hue changes (cyanopia)
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3
Q

What is the MOA of flutamide?

Use?

A

Flutamide

  • competitive inhibitor at androgen receptors
  • used to treat prostate cancer
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4
Q

MOA of danazol

Use (2)

A

Danazol

  • Partial agonist at androgen receptors
  • Treats endometriosis and hereditary angioedema
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5
Q

What are tocolytics?

Give 3 examples

A

Tocolytics

  • Medications that relax the uterus
  • Terbutaline (beta2 agonist)
  • Nifedipine (CCB)
  • Indomethacin (NSAID)
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6
Q

Why do we administer steroids to women in preterm labor?

What drug allows us to give steroids prior to birth?

A

Steroids increase fetal lung maturity & surfactant production

Tocolytics give us enough time to administer steroids

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7
Q

What is the mechanism of mifepristone?

Use?

A

Mifepristone

  • Competitive inhibitor of progesterone receptor
  • Used together with misoprostol to terminate pregnancy
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8
Q

What is the mechanism and use of ulipristal?

A
  • Ulipristal is a competitive progesterone blocker that delays ovulation
  • Used for emergency contraception
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9
Q

What is the most effective form of emergency contraception?

A

Copper IUD

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10
Q

What drug is given in the case of postpartum hemorrhage?

Why?

A

Oxytocin

(promotes contraction of smooth muscle)

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11
Q

Which GPCR causes relaxation/dilation of cervix & uterus?

What GPCR causes contraction?

A
  • Gq - contraction
  • Gs - relaxation & dilation
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12
Q

What signaling molecule class is responsible for cervical dilation?

A

PG’s

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13
Q

Uterine contraction is stimulated by ___’s and ____ (hormone) via opening of ___________

A

Uterine contraction is stimulated by PG’s and oxytocin via opening of L-type calcium channels

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