Pharm 4 Flashcards

1
Q

alpha1

A

vasoconstriction (by inc smooth muscle tone so inc BP), urinary retention, mydriasis (dilation)

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2
Q

beta1

A

inc HR and force of constraction, thus positive ionotropic and chronotropic actions

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3
Q

beta2

A

bronchodilation (smooth muscle) and vasodilation of skeletal blood vessels

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4
Q

alpha 1 block

A

vasodilation

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5
Q

beta1 block

A

dec HR

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6
Q

beta 2 block

A

bronchoconstriction

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7
Q

levadopa

A

for parkinsons. levodopa is precursor to dopamine but can cross BBB. give with carbadopa (sacrificial) for dopa decarboxylase in periphery. levadopa is sympathomimetic and will create sympathetic issues in periphery
Side effects: abnormal facial movements, naseau, vomiting, cardiac arrythmia, and mental disturbances

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8
Q

alpha2

A

given orally they cause hypotension by reducing sympathetic outflow from CNS

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9
Q

eye sympathetic

A

mydriasis or relaxation of ciliary muscles

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10
Q

heart symp

A

acceleration and inc contraction

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11
Q

vascular smooth muscle symp

A

vasoconstriction

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12
Q

bronchiolar smooth muscle symp

A

relaxation/bronchodilation

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13
Q

sweat glands symp

A

sweating

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14
Q

alpha blockers

A

-sin, phentolamine, chlopromazine

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15
Q

most potent bronshodilator of sympathetics

A

isoproterenol

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16
Q

vasoconstriction of gingival vessels

A

levonordefrin, epi, phenylephrine

17
Q

pharmacological agonist

A

binds to a specific receptor and produces a response

18
Q

efficacy

A

drug that causes the greatest maximum effect

19
Q

LD50

A

mean lethal dose

20
Q

ED50

A

mean effective dose

21
Q

theraputic index

A

LD50/ED50

22
Q

physiological antagonism

A

two drugs produce opposite effects but dont act on same receptor (epi/histamine, and epi/nitroglycerin)

23
Q

synergism

A

combo effect is greater than two effects added together

24
Q

idiosyncrisy reactions

A

genetically determined abnormal responses to drugs. related to species, genetics, age

25
Q

potency

A

amount of drug compared to resposne

26
Q

effective antagonist

A

no intrinsic activity and high affinity

27
Q

benzodiazapines

A

sedatives (diazapam, chlordiazopoxide) modulate inhibitory neurotransmitter GABA. advantages over barbituates (less addictive potential, less profound CNS depression, larger therapeutic index, less respiratory depression). many BDZ form active metabolites, IV injection can cause thromobphlebitis (from solvent IV is dissolved in)

28
Q

Barbituates

A

sedative metabolized by liver. thiopental ( rapidly redistribution from brain (rapid in and out) quick onset and short duration). barbs are not analgesic. overdose kills from respiratory depression. contraindicated in pt with intermittent porphyria (enhance porphyria synthesis so make it worse), emphysema, and undiagnsoed severe pain. side effects inc seretions (saliva and bronchiol)

29
Q

antipsychotics; first gen

A

phenothiazines, chlorpromazine, haloperidol. blocakde of dopaminergic sites in the brain. side effects: anticholinergic, extrapyramidal effects resulting in taardive dyskensia, jaundice, photosensitivity, antiadregenergic affect hypothalaic temp reg system

30
Q

second gen antipsychotics

A

clozapine. block dopamine and serotonin (5-HT) receptors. treat negative as well as positive symptoms. fewer extrapyramidal side effects like tardive dyskensia. affect hypothal temp reg system