Midterm 1 Drugs to Know Flashcards

(59 cards)

1
Q

cocaine

A

topical anesthetic

drug crosses membrane - non-ionized and lipid-soluble;
drug becomes ionized inside cell and temporarily blocks Na channel; depolarization cannot occur with blocked Na channel; pain signal cannot be sent “downstream”; local cellular enzymes break down the anesthetic over time;
*indirect acting adrenergic; blocks re-uptake of norepinephrine; potentiates adrenergic (sympathetic) activity; results in mydriasis and vasoconstriction\

mydriatic

indirect acting adrenergic agonist; inhibits reuptake of NE; causes mydriasis and vasoconstriction; only about 2 mm of mydriasis

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2
Q

tetracaine

A

topical anesthetic

drug crosses membrane - non-ionized and lipid-soluble;
drug becomes ionized inside cell and temporarily blocks Na channel; depolarization cannot occur with blocked Na channel; pain signal cannot be sent “downstream”; local cellular enzymes break down the anesthetic over time

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3
Q

benoxinate

A

topical anesthetic

drug crosses membrane - non-ionized and lipid-soluble;
drug becomes ionized inside cell and temporarily blocks Na channel; depolarization cannot occur with blocked Na channel; pain signal cannot be sent “downstream”; local cellular enzymes break down the anesthetic over time

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4
Q

proparacaine

A

topical anesthetic

drug crosses membrane - non-ionized and lipid-soluble;
drug becomes ionized inside cell and temporarily blocks Na channel; depolarization cannot occur with blocked Na channel; pain signal cannot be sent “downstream”; local cellular enzymes break down the anesthetic over time

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5
Q

lidocaine

A

topical anesthetic

drug crosses membrane - non-ionized and lipid-soluble;
drug becomes ionized inside cell and temporarily blocks Na channel; depolarization cannot occur with blocked Na channel; pain signal cannot be sent “downstream”

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6
Q

procaine hydrochloride (novacain)

A

injection anesthetic

drug crosses membrane - non-ionized and lipid-soluble;
drug becomes ionized inside cell and temporarily blocks Na channel; depolarization cannot occur with blocked Na channel; pain signal cannot be sent “downstream”

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7
Q

lidocaine hydrochloride (xylocain)

A

injection anesthetic

drug crosses membrane - non-ionized and lipid-soluble;
drug becomes ionized inside cell and temporarily blocks Na channel; depolarization cannot occur with blocked Na channel; pain signal cannot be sent “downstream”

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8
Q

mepivacaine hydrochloride (carbocaine)

A

injection anesthetic

drug crosses membrane - non-ionized and lipid-soluble;
drug becomes ionized inside cell and temporarily blocks Na channel; depolarization cannot occur with blocked Na channel; pain signal cannot be sent “downstream”

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9
Q

bupivacaine hydrochloride (marcaine)

A

injection anesthetic

drug crosses membrane - non-ionized and lipid-soluble;
drug becomes ionized inside cell and temporarily blocks Na channel; depolarization cannot occur with blocked Na channel; pain signal cannot be sent “downstream”

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10
Q

epinephrine

A

vasoconstrictor added in combination with injection anesthetics; prolongs duration, decreases systemic absorption, decreases bleeding

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11
Q

pilocarpine

A

miotic

muscarinic cholinergic agonist; iris sphincter contraction- pupil constriction; ciliary muscle contraction- accommodation and increased aqueous flow

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12
Q

scopolamine

A

cycloplegic

cholinergic antagonist- blocks ACh receptors, decreasing parasympathetic activity, increases sympathetic activity;
causes pupil dilation and paresis of accommodation

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13
Q

tropicamide

A

cycloplegic

cholinergic antagonist- blocks ACh receptors, decreasing parasympathetic activity, increases sympathetic activity;
causes pupil dilation and paresis of accommodation

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14
Q

atropine

A

cycloplegic

cholinergic antagonist- blocks ACh receptors, decreasing parasympathetic activity, increases sympathetic activity;
causes pupil dilation and paresis of accommodation

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15
Q

cyclopentolate

A

cycloplegic

cholinergic antagonist- blocks ACh receptors, decreasing parasympathetic activity, increases sympathetic activity;
causes pupil dilation and paresis of accommodation

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16
Q

homatropine

A

cycloplegic

cholinergic antagonist- blocks ACh receptors, decreasing parasympathetic activity, increases sympathetic activity;
causes pupil dilation and paresis of accommodation

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17
Q

phenylephrine

A

mydriatic

direct-acting alpha 1 agonist; mimics effects of NE; stimulates iris dilator muscle; produces conjunctival vasoconstriction

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18
Q

hydroxyamphetamine

A

mydriatic

indirect acting adrenergic agonist; inhibits reuptake of NE with some stimulation of NE release

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19
Q

dapiprazole (Rev-Eyes)

A

mydriolytic

adrenergic antagonist; blocks adrenergic receptors; causes miosis; “reversal of dilation”

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20
Q

Durezol

difluprednate 0.05%

A

topical corticosteroid

inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins

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21
Q

Pred Forte, Omni Pred

prednisolone acetate 1%

A

topical corticosteroid

inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins

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22
Q

Pred Mild

prednisolone acetate 0.1%

A

topical corticosteroid

inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins

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23
Q

Inflamase Forte

prednisolone sodium phosphate 1%

A

topical corticosteroid

inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins

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24
Q

FML

fluorometholone alcohol 0.1%

A

topical corticosteroid

inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins

25
FML Forte | fluorometholone alcohol 0.25%
topical corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
26
Flarex | fluorometholone acetate 0.1%
topical corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
27
Maxidex | dexamethasone 0.1%
topical corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
28
Alrex | loteprednol 0.2%
topical corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
29
Lotemax | loteprednol 0.5%
topical corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
30
Lotemax SM | loteprednol 0.38%
topical corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
31
Eysuvis | loteprednol 0.25%
topical corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
32
Inveltys | loteprednol 1%
topical corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
33
Kenalog | triamcinolone
injectable corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
34
Retisert
implantable corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
35
Iluvien
implantable corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
36
Ozurdex
implantable corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
37
Dextenza
implantable corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
38
Prednisone
oral corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
39
Medrol | methylprednisolone
oral corticosteroid inhibits phospholipase A2 which decreases synthesis of prostaglandins and leukotrienes; decreases synthesis of cyclooxygenase-2 which decreases synthesis of prostaglandins
40
Acular | ketorolac 0.5%
topical NSAID inhibits the synthesis of prostaglandins: inhibits cyclooxygenase enzymes which leads to decreased prostaglandin synthesis
41
Acuvail | ketorolac 0.45%
topical NSAID inhibits the synthesis of prostaglandins: inhibits cyclooxygenase enzymes which leads to decreased prostaglandin synthesis
42
Bromsite | bromfenac 0.075%
topical NSAID inhibits the synthesis of prostaglandins: inhibits cyclooxygenase enzymes which leads to decreased prostaglandin synthesis
43
Prolensa | bromfenac 0.07%
topical NSAID inhibits the synthesis of prostaglandins: inhibits cyclooxygenase enzymes which leads to decreased prostaglandin synthesis
44
Ilevro | nepafenac 0.3% susp
topical NSAID inhibits the synthesis of prostaglandins: inhibits cyclooxygenase enzymes which leads to decreased prostaglandin synthesis
45
Nevanac | nepafanac 0.1% susp
topical NSAID inhibits the synthesis of prostaglandins: inhibits cyclooxygenase enzymes which leads to decreased prostaglandin synthesis
46
Voltaren | dicolefenac 0.1% susp, 1% gel
topical NSAID inhibits the synthesis of prostaglandins: inhibits cyclooxygenase enzymes which leads to decreased prostaglandin synthesis
47
ibuprofen
oral NSAID inhibits the synthesis of prostaglandins: inhibits cyclooxygenase enzymes which leads to decreased prostaglandin synthesis
48
indomethacin
oral NSAID inhibits the synthesis of prostaglandins: inhibits cyclooxygenase enzymes which leads to decreased prostaglandin synthesis
49
aceteaminophen
oral pain relief inhibits prostaglandin synthesis similar to COX-2 specific drugs (higher activity in the CNS); good antipyretic and analgesic
50
codeine
opioid binds to opiate receptors in spinal cord, decreasing conduction of pain signal to the brain; also binds to opiate receptors in the brain, causing sedation and euphoria
51
hydrocodone
opioid binds to opiate receptors in spinal cord, decreasing conduction of pain signal to the brain; also binds to opiate receptors in the brain, causing sedation and euphoria
52
oxycodone
opioid binds to opiate receptors in spinal cord, decreasing conduction of pain signal to the brain; also binds to opiate receptors in the brain, causing sedation and euphoria
53
tramadol
opioid binds to opiate receptors in spinal cord, decreasing conduction of pain signal to the brain; also binds to opiate receptors in the brain, causing sedation and euphoria also a weak inhibitor of serotonin and norepinephrine reuptake
54
buprenorphine
opioid partial agonist; acts like morphine in patients who have not taken opioids; causes withdrawal in users of full opioid agonists
55
naloxone
opioid antagonist rapidly displaces all receptor-bound opioid molecules; reverses the effect of overdose
56
Lortab
hydrocodone + acetaminophen
57
Percocet
oxycodone + acetaminophen
58
Percodan
oxycodone + acetylsalicylic acid
59
Tylenol #__
codeine + acetaminophen