PSCEP Review with Dr. Torres Flashcards

1
Q

This is an amphetamine variant whose major pharmacologic effects and abuse potential are similar to those of amphetamine, but this may be effective in children with attention deficit hyperactivity disorder

A

Methylphenidate

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2
Q

This is a selective inhibitor of the norepinephrine reuptake transporter. Its actions, therefore, are mediated by potentiation of norepinephrine levels in noradrenergic synapses. It is used in the treatment of attention deficit disorders

A

Atomoxetine

Atomoxetine has surprisingly little cardiovascular effect because it has a clonidine-like effect in the CNS to decrease sympathetic outflow while at the same time potentiating the effects of norepinephrine in the periphery.

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3
Q

This is a psychostimulant indirect-acting sympathomimetic that differs from amphetamine in structure, neurochemical profile, and behavioral effects. It is used primarily to improve wakefulness in narcolepsy and some other conditions as it inhibits dopamine and norepinephrine transporters, while decreasing GABA levels.

A

Modafinil

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4
Q

This is a potent competitive antagonist at both α1 and α2 receptors, and is used for pheochromocytoma diagnostics, the Regitine test

A

Phentolamine

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5
Q

Drug used for Tensilon test for Myasthenia gravis

A

Edrophonium

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6
Q

This is the study of genetic factors that underlie variation in drug response.

A

Pharmacogenomics or Pharmacogenetics

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7
Q

This is the RANKL inhibitor that is of comparable efficacy to bisphosphonates in the treatment of postmenopausal osteoporosis. It is given subcutaneously every 6-months in 60-mg doses.

A

Denosumab

Like the bisphosphonates it suppresses bone resorption and secondarily bone formation. Denosumab reduces the risk of both vertebral and nonvertebral fractures with comparable effectiveness to the potent bisphosphonates.

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8
Q

This is the selective estrogen receptor modulator (SERM) approved for treatment of osteoporosis. It reduces the risk of breast cancer and protects against spine fractures but not hip fractures.

A

Raloxifene

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9
Q

Nonhormonal agents that suppress the activity of osteoclasts in part via inhibition of farnesyl pyrophosphate synthesis; used for osteoporosis

A

Bisphosphonates (ex. alendronate)

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10
Q

This is the newest bone-building medicine to treat osteoporosis, and it is highly effective at treating this condition by blocking the protein sclerostin, which is produced by bone cells and negatively impacts bone density. Administered as monthly injections, the drug helps to increase bone density and lower fracture risk.

A

Romosozumab

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11
Q

Wernicke-Korsakoff syndrome is a relatively uncommon but important entity characterized by paralysis of the external eye muscles, ataxia, and a confused state that can progress to coma and death. It is associated with ____________ deficiency but is rarely seen in the absence of alcoholism.

A

thiamine
vitamin B1

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12
Q

This is an irreversible α-adrenoceptor antagonist, is used to control the hypertension by indirect baroreceptor activation caused by catecholamines released from pheochromocytoma, a tumor of the adrenal medulla.

A

Phenoxybenzamine

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13
Q

This is a competitive piperazinyl quinazoline effective in the management of hypertension. It is highly selective for α1 receptors and typically 1000-fold less potent at α2 receptors. This may partially explain the relative absence of tachycardia seen with this drug compared with that of phentolamine and phenoxybenzamine. It also relaxes both arterial and venous vascular smooth muscle, as well as smooth muscle in the prostate, due to blockade of α1 receptors. Hence, it is used for BPH with hypertension

A

Prazosin

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14
Q

The first commercial preparation of PGI2 approved for the treatment of pulmonary hypertension, improves symptoms, prolongs survival, and delays or prevents the need for lung or lung-heart transplantation.

A

Epoprostenol

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15
Q

___________, an agonist at 5-HT1B/1D, is currently first-line therapy for acute severe migraine attacks in most patients. However, it should not be used in patients at risk for coronary artery disease.

A

Sumatriptan

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16
Q

The third generation of antihistamines presently consists of:

A

FEXOFENADINE, norastemizole and DCL

17
Q

__________ is a new second generation H1-antihistamine recently approved for the symptomatic treatment of allergic rhinitis and chronic urticaria

A

Bilastine

18
Q

An antidepressant effective for smoking cessation by noncompetitive antagonism of nicotinic receptors, replacing varenicline

A

Bupropion

Bupropion is also combined with naltrexone (opioid antagonist) for anti-obesity.

19
Q

This is done for resuscitation from bupivacaine cardiotoxicity

A

Intravenous lipid emulsion (ILE)

20
Q

A novel approach to treat orthostatic hypotension is ___________, a synthetic molecule that has been approved by the FDA to treat neurogenic orthostatic hypotension.

A

Droxidopa

21
Q

This is a nonselective beta-blocker with no local anesthetic activity. It has excellent ocular hypotensive effects when administered topically in the eye.

A

Timolol

22
Q

This neurotoxin produces chemodenervation and local paralysis when injected into a muscle.

A

Botulinum toxin

23
Q

A special application of dantrolene is in the treatment of ________________, a rare heritable disorder that can be triggered by a variety of stimuli, including general anesthetics (eg, volatile anesthetics) and neuromuscular blocking drugs (eg, succinylcholine)

A

malignant hyperthermia

24
Q

This is the most widely used somatostatin analog useful for the acute control of bleeding from esophageal varices.

A

Octreotide

25
Q

Betablocker used to prevent esophageal varices for people with portal hypertension

A

Propranolol

26
Q

SERM extensively used in the palliative treatment of breast cancer in postmenopausal women and is approved for chemoprevention of breast cancer in high-risk women

A

Tamoxifen

27
Q

_______________, a selective nonsteroidal inhibitor of aromatase (the enzyme required for estrogen synthesis), is effective in some women whose breast tumors have become resistant to tamoxifen

A

Anastrozole

28
Q

This is a pure estrogen receptor antagonist that has been somewhat more effective than those with partial agonist effects in some patients who have become resistant to tamoxifen.

A

Fulvestrant

29
Q

GnRH agonists can be administered via nasal spray

A

nafarelin

30
Q

A new amphetamine substitute that is approved for use in narcolepsy and is claimed to have fewer disadvantages (excessive mood changes, insomnia, and abuse potential) than amphetamine in this condition

A

Modafinil

31
Q

This is an α2 agonist used for sedation under intensive care circumstances and during anesthesia

A

Dexmedetomidine