Pharm Flashcards

1
Q

Ropinirole

A

D2 R agonist used to tx PD

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2
Q

Pramipexole

A

D R agonist used to tx PD, relative D3 affinity

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3
Q

Rotigotine

A

D R agonist used to tx early PD. Skin patch

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4
Q

in PD, the ____ pathway predominates

A

indirect

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5
Q

5 strategies in PD pharm therapy

A

replace DA, stim D Rs, enhance DA release, inhibit DA metabolism, alter DA/Ach balance

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6
Q

Selegiline

A

MAO-B inhibitor. Tx PD. May have neuroprotective effects. Used when Ldopa response has declined. Little effect when used alone

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7
Q

Rasagiline

A

more potent MAO-B inhibitor. For combined therapy with levodopa in late stage PD or alone early in PD

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8
Q

Do not take meperidine, TCAs, SSRIs with

A

Selegiline

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9
Q

Metabolized by CYP1a2

A

Ropinirole - D R agonist (D2)

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10
Q

COMT inhibitors

A

entacapone, tolcapone - inhibit DA metab. increase bioavail of Ldopa, reduces fluctuations in response

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11
Q

only has peripheral COMT inhib effect

A

entacapone. Tolcapone is central and peripheral

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12
Q

AE tolcapone

A

increased liver enzymes and hepatic failure

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13
Q

Muscarinic antagonists used in PD

A

benztropine, diphenhydramine, trihexyphenidyl - early PD or adjunct to Ldopa

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14
Q

AE of musc antags for PD

A

typical anticholinergic effects, drows, inattention, confusion, delusions, halluc, mood change

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15
Q

Contraindications of musc antags used in PD

A

prostatic hyperplasia, OBD, glaucoma, avoid use with other drugs with antimusc effects (TCAs, antihistamines)

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16
Q

calcium channel blocker of the dihydropyridine class. It is usually prescribed for the treatment of high blood pressure in order to reduce the risk of stroke and heart attack. More recent research in animal models suggests that isradipine may have potential uses for treating Parkinson’s disease

A

Isradipine

17
Q

Drugs for Huntingtons are aimed at

A

treating the depression - Fluoxetine, Carbamazepine. Reserpine and tetrabenazine (central dopamine depleting agents) may help with chorea - increase act of indir pathway by blocking D2)

18
Q

mu R endogenous opioid peptide

A

endorphins > enkeph > dynorph

19
Q

delta R endogenous opioid peptide

A

enkephalin

20
Q

kappa R endogenous opioid peptide

A

dynorphin

21
Q

main reservoir for opiate distribution

A

skeletal muscle

22
Q

AE of opioids that do not demonstrate tolerance

A

miosis, constipation, convulsions. Moderate for bradycardia

23
Q

increased CNS depression with opioids when given with

A

sedative hypnotics, antipsychotic tranquilizers, monoamine oxidase inhibitors (increased risk hyperpyrexic coma)

24
Q

codeine converted to morphine via

A

CYP2D6

25
Q

lack active metabolites and could be considered in the setting of renal failure

A

hydromorphone and fentanyl

26
Q

opioids work in

A

ventral tegmental neurons which lead to increased dopaminergic activation in the nucleus accumbens

27
Q

tox of capsaicin

A

increased pain, burning eyes or mucus membranes

28
Q

tox of cod liver

A

increased bleeding risk oral anti-coag, additive with antihypertensive, increased blood sugar

29
Q

tox of devil’s claw

A

adversely affects acid inhibiting, BP and CV drugs

30
Q

tox of epsom salts

A

GI irritation, drug interactions affecting excretion and skeletal muscle relaxants

31
Q

tox of white willow

A

contains salicyclates, potential interaction with anticoagulants, antiplatelet and oral drugs