Drug recognition Flashcards

(59 cards)

1
Q

fluoxetine

A

5-HT reuptake inhibitor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

fluvoxamine

A

5-HT reuptake inhibitor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

trazodone

A

5-HT reuptake inhibitor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

imipramine

A

5-HT reuptake inhibitor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

spiroperidol

A

DA 2 receptor antagonist- antipsychotic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

haloperidol

A

DA 2 receptor antagonist- antipsychotic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

desipramine

A

selective NE reuptake inhibitor (SNRI)

Treats depression. This medicine is a tricyclic antidepressant.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

maprotyline

A

selective NE reuptake inhibitor (SNRI)

Treats depression and anxiety. This medicine is a tricyclic antidepressant.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

protryptiline

A

selective NE reuptake inhibitor (SNRI)

is a tricyclic antidepressant (TCA), indicated for the treatment of depression and ADHD.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

L-dopa + carbidopa

A

L-dopa + carbidopa= Sinemet

Combination drug for the treatment of Parkinson’s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

pimozide

A

DA 2 receptor antagonist- antipsychotic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

barbiturates

A

stimulate GABA and increase DURATION of the Cl- channel opening

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

diazepam

A

(Valium) benzodiazepine- bind to another site on GABA and increase the FREQUENCY of Cl- channel opening

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

lorazepam

A

(Ativan) benzodiazepine- bind to another site on GABA and increase the FREQUENCY of Cl- channel opening

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

tetrodotoxin

A

(from puffer fish) Na+ channel blocker

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

alpha bungarotoxin

A

nicotinic ACh receptor blocker

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

picrototoxin

A

GABAa receptor blocker

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

strychnine

A

glycine receptor blocker

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

cocaine

A

NE, dopamine, 5-HT reuptake inhibiter

mesolimbic pathway

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

amphetamine and methamphetamine

A

stimulate release of dopamine (also NE and 5-HT)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

LSD

A

5-HT receptor agonist

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

hemicholinium

A

prevents the presynaptic REUPTAKE of choline

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

vesamicol

A

prevents the STORAGE of ACh in vesicles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

botulinum toxin

A

prevents the fusion and RELEASE of ACh into the synaptic cleft

25
metyrosine
prevents production of dopa from tyrosine by inhibiting tyrosine hydroxylase
26
reserpine
inhibits NE storage by inhibiting VMAT
27
Guanethidine, bretylium
prevents fusion of vesicles and release of NE
28
tricyclic antidepressants, cocaine
prevent the reuptake of NE
29
Clonidine
Clonidine and guanabenz are alpha 2 agonists. Centrally acting, and decrease central sympathetic outflow. Remember that alpha2 is an AUTORECEPTOR and is inhibitory.
30
Prazosin
Prazosin - Alpha 1 antagonist dilates arteries and veins These do a great job managing hypertension, and they also decrease the urethral tone and help to alleviate bladder outlet obstruction in BPH.
31
Metoprolol
Selective beta1 adrenergic antagonist
32
Atenolol
Selective beta1 adrenergic antagonist
33
Nebivolol
Highly selective beta1 adrenergic antagonist, also a vasodilator
34
Propranolol
Non-selective beta adrenergic antagonists
35
nadolol
Non-selective beta adrenergic antagonists
36
timolol
Non-selective beta adrenergic antagonists for treatment of glaucoma
37
Phenoxybenzamine (POB)
Irreversible blockade of Alpha 1 and 2 receptors, which also blocks the negative feedback mechanism of alpha 2. Epi and NE build up and act on beta 1 and 2 to increase BP and HR... Given for symptomatic management of pheochromocytoma- a tumor of the adrenal medulla that results in excess secretion of epi/NE Side effects (and toxicity) include orthostatic hypertension and reflex tachycardia.
38
Carvedilol
Mixed alpha/beta antagonist, more effective at beta than alpha1, and works well for CHF with decreased systolic function.
39
terazosine
selective alpha 1 blocker. Great for treatment of hypertension and urinary retention in BPH
40
Labetalol
Mixed alpha/beta antagonist. Great for treatment of hypertensive emergencies and pregnancy associated hypertension. May induce hepatitis, and that sort of sucks...
41
Pilocarpine
Muscarinic agonist that is an alkaloid, well absorbed (crosses BBB due to no charge) and great for treatment of glaucoma and Sjögren's syndrome. Potent stimulator of sweat, tears and saliva.
42
Methacholine
Muscarinic agonist, choline ester that is used in challenge test for diagnosis of asthma. Stimulates muscarinic receptors in the airway when inhaled.
43
Carbachol
Muscarinic agonist, choline ester that is used for the treatment of glaucoma and for miosis induction for eye surgeries.
44
Bethanechol
Muscarinic agonist, choline ester that is used for the relief of urinary retention and increased GI motility
45
Atropine
Muscarinic antagonist (non-selective M). Reversible inhibitor of muscarinic receptors. It is a tertiary alkaloid, and can therefore cross the BBB ``` Causes: Mydriasis, cycloplegia Decreased airway secretions Decreases gastric secretions Decreased gut motility Urinary retention ```
46
Scopolamine
Naturally occurring tertiary alkaloid muscarinic antagonist. Clinically used prophylactically for motion sickness and post-op nausea and vomiting.
47
Ipatropium
Semisynthetic alkaloid (non selective M) muscarinic antagonist. doesn't cross into CNS. Used for the treatment of bronchial asthma, COPD and maybe nasal discharge.
48
Tiotropium
Semisynthetic alkaloid (selective M1,M3) muscarinic antagonist. doesn't cross into CNS. Used for the treatment of bronchial asthma, COPD
49
Tolterodine
Synthetic M3 selective muscarinic antagonist for the treatment of urinary incontinence.
50
Nicotine
Tertiary alkaloid nicotinic agonist. Only clinical use is smoking cessation.
51
Lobeline
Tertiary alkaloid nicotinic agonist. No clinical use.
52
Succinylcholine
Choline ester nicotinic agonist. Used for neuromuscular blockade in surgery and rapid sequence intubation. Very resistant to AChE and eventually the channel becomes unresponsive, even after agonist removal. Causes paralysis.
53
Hexamethonium
Nicotinic ganglion blocking agent. Nondepolarizing competitive antagonist that binds directly to the nicotinic ion channel in the autonomic ganglia, thereby blocking all parasympathetic and sympathetic stuff. Not clinically used due to side effects.
54
Trimethaphan
Nicotinic ganglion blocking agent. Nondepolarizing competitive antagonist that blocks the nicotinic receptor in the autonomic ganglia, thereby blocking all parasympathetic and sympathetic stuff. Not clinically used due to side effects.
55
Edrophonium
ChE inhibitor. Simple alcohol with quaternary ammonium group. Reversible, and very short-acting (2-10 min). Used in the diagnosis of myasthenia gravis. When injected, symptoms should decrease for a few minutes and then return.
56
Neostigmine
ChE inhibitor. Carbamic ester of alcohol with quaternary ammonium group. Reversible, with action from 30 minutes to 6 hours. No crossing into CNS. Used for non-depolarizing reversal of neuromuscular blockade (post-op). Also used to treat myasthenia gravis, but not as good as pyridostigmine...
57
pyridostigmine
ChE inhibitor. Carbamic ester of alcohol with quaternary ammonium group. Reversible, with action from 30 minutes to 6 hours. No crossing into CNS. Best drug for treatment of myasthenia gravis. Can also be used prophylactically (along with atropine) for treatment of organophosphate poisoning.
58
Physostigmine
ChE inhibitor. Carbamic ester of alcohol with quaternary ammonium group. Reversible, with action from 30 minutes to 6 hours. DOES cross into CNS. Used for reversal of anticholinergic toxicity (too much atropine...) Also useful for glaucoma treatment.
59
Echothiophate
ChE inhibitor. Organophosphate covalently binds irreversibly to ChE. Not a great idea to use this one clinically, but if you're interested in inhumane warfare, it is a must have along with sarin gas. Organophosphate "aging" occurs when the alkyl group is lost and the phosphate bond gets even stronger.