Genitourinary Flashcards

1
Q

Darifenacin

A

Anticholinergic

Reduce bladder muscle contractility, increase
bladder capacity

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2
Q

Oxybutynin

A

Anticholinergic

Reduce bladder muscle contractility, increase
bladder capacity

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3
Q

Propantheline

A

Anticholinergic

Reduce bladder muscle contractility, increase
bladder capacity

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4
Q

Solifenacin

A

Anticholinergic

Reduce bladder muscle contractility, increase
bladder capacity

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5
Q

Tolterodine

A

Anticholinergic

Reduce bladder muscle contractility, increase
bladder capacity

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6
Q

Mirabegon

A

Beta3-adrenoreceptor agonist; relaxes bladder muscle during the storage phase of micturition, increasing bladder capacity.

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7
Q

Desmopressin

A

Antidiuretic hormone analogue

Used in nocturnal enuresis in children

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8
Q

Alfuzosin

A

Block alpha1 receptors, relaxing smooth muscle in the bladder neck and prostate, and decreasing resistance to urinary flow.

Unlike nonselective alpha-blockers (eg phenoxybenzamine), they have little effect on presynaptic alpha2 receptors and are therefore less likely to cause reflex tachycardia.

Alfuzosin, silodosin and tamsulosin are more selective for the alpha1-receptor subtypes found in the bladder and prostate.

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9
Q

Silodosin

A

Block alpha1 receptors, relaxing smooth muscle in the bladder neck and prostate, and decreasing resistance to urinary flow.

Unlike nonselective alpha-blockers (eg phenoxybenzamine), they have little effect on presynaptic alpha2 receptors and are therefore less likely to cause reflex tachycardia.

Alfuzosin, silodosin and tamsulosin are more selective for the alpha1-receptor subtypes found in the bladder and prostate.

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10
Q

Tamsulosin

A

Block alpha1 receptors, relaxing smooth muscle in the bladder neck and prostate, and decreasing resistance to urinary flow.

Unlike nonselective alpha-blockers (eg phenoxybenzamine), they have little effect on presynaptic alpha2 receptors and are therefore less likely to cause reflex tachycardia.

Alfuzosin, silodosin and tamsulosin are more selective for the alpha1-receptor subtypes found in the bladder and prostate.

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11
Q

Dutasteride

A

Inhibit 5‑alpha-reductase, which converts testosterone to dihydrotestosterone (a potent cellular androgen that stimulates prostate growth). They reduce prostate size and improve symptoms and urinary flow rate.

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12
Q

Finasteride

A

Inhibit 5‑alpha-reductase, which converts testosterone to dihydrotestosterone (a potent cellular androgen that stimulates prostate growth). They reduce prostate size and improve symptoms and urinary flow rate.

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13
Q

Avanafil

A

Phosphodiesterase 5 inhibitor

Sexual stimulation increases cyclic guanosine monophosphate (cGMP) levels, resulting in smooth muscle relaxation, inflow of blood to the corpus cavernosum and penile erection.

These agents inhibit the breakdown of cGMP by phosphodiesterase 5 (PDE5), increasing blood flow to the penis during sexual stimulation.

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14
Q

Sildenafil

A

Phosphodiesterase 5 inhibitor

Sexual stimulation increases cyclic guanosine monophosphate (cGMP) levels, resulting in smooth muscle relaxation, inflow of blood to the corpus cavernosum and penile erection.

These agents inhibit the breakdown of cGMP by phosphodiesterase 5 (PDE5), increasing blood flow to the penis during sexual stimulation.

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15
Q

Tadalafil

A

Phosphodiesterase 5 inhibitor

Sexual stimulation increases cyclic guanosine monophosphate (cGMP) levels, resulting in smooth muscle relaxation, inflow of blood to the corpus cavernosum and penile erection.

These agents inhibit the breakdown of cGMP by phosphodiesterase 5 (PDE5), increasing blood flow to the penis during sexual stimulation.

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16
Q

Alprostadil

A

Prostaglandin E1

Dilates cavernosal arteries. Relaxes smooth muscle of corpus cavernosum and spongiosum.

17
Q

Dapoxetine

A

Unclear; an SSRI thought to modulate the ejaculatory reflex.

18
Q

Papaverine

A

Relaxation of all vascular components of the penile erectile system.