PSCEP Review with Dr. Torres Flashcards
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
Methylphenidate
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
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.
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.
Modafinil
This is a potent competitive antagonist at both α1 and α2 receptors, and is used for pheochromocytoma diagnostics, the Regitine test
Phentolamine
Drug used for Tensilon test for Myasthenia gravis
Edrophonium
This is the study of genetic factors that underlie variation in drug response.
Pharmacogenomics or Pharmacogenetics
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.
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.
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.
Raloxifene
Nonhormonal agents that suppress the activity of osteoclasts in part via inhibition of farnesyl pyrophosphate synthesis; used for osteoporosis
Bisphosphonates (ex. alendronate)
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.
Romosozumab
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.
thiamine
vitamin B1
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.
Phenoxybenzamine
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
Prazosin
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.
Epoprostenol
___________, 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.
Sumatriptan