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Hy Kaplan Notes
Hy Kaplan Notes
Characteristic Disease
1st line tx for a fibrillation is : Digoxin
how does digoxin help in a fibrillation ? decreases conduction through AV node
treatment for C. difficile metronidazole
why doesn't gentamicin work for C. diff? gentamicin = aminoglycoside that only works for gram (-)
infections
most common cause of drug-induced thrombocytopenia : heparin
anticoagulant associated with development of ProC deficiency : warfarin
kernicterus can result when pregnant women are given (TMS)___ in the third trimester TMP-sulfa
associated with "gray baby syndrome" when given to pregnant women : chloramphenicol
topical ointment often used in the prophylaxis of infections in burn patients: silver sulfadiazine cream
appropriate pharmacologic tx for DIC : heparin
antidote for acetaminophen OD : acetylcysteine
chelating agent used to treat OD with copper, lead, gold, and other metals: penacillamine
given to people who OD( overdose) on heparin protamine Sulfate.
acetylcholinesterase reactivator used in organophosphate poisoning : pralidoxime
antiarrythmic which can cause drug-induced lupus: procainamide
other drugs that can cause drug-induced lupus : hydralazine, quinine, INH, methyldopa
drug that causes release of factor VIII from storage sites: desmopressin
drug that specifically inhibits the translocation in CML: imanitib mesylate (Gleevac)
neurotransmitter affected by sertraline : serotonin (SSRI)
type of antibiotic likely to exacerbate MG( Myastenia Gravis) aminoglycosides (risk for neuromuscular
blockade)
drug used to diagnose MG : edrophonium
most appropriate treatment of Klebsiella pneumonia : cefotaxime IV
most appropriate treatment of Legionella pneumonia : erythromycin IV
drugs that potentiate the effects of warfarin : quinolones, erythromycin, sulfas, and metronidazole
mucolytic used in the treatment of CF( Cystic Fibrosis) : N-acetylcysteine
tricyclic antidepressant which may cause hyperprolactinemia: nortriptyline
anti-Parkinson's drug that affects dopamine: selegiline
mechanism of selegiline:Monoamine Oxidase B inhibitor( MAO-B inhibitor ) _ (slows metabolism of
dopa)
β- 1 blocker which does NOT exacerbate asthma (3) atenolol, metoprolol, esmolol
Atenolol - Clinical Pharmacology
Atenolol is a beta1-selective (cardioselective) beta-adrenergic receptor blocking agent without
membrane stabilizing or intrinsic sympathomimetic (partial agonist) activities. This preferential effect is
not absolute, however, and at higher doses, Atenolol inhibits beta2-adrenoreceptors, chiefly located in
the bronchial and vascular musculature.
two main Abx used for anaerobes metronidazole and clindamycin. Abx( Antibiotics).
streptokinase binds to : plasminogen
mechanism of cocaine blocks reuptake of NE
two drugs that increase the activity of lipoprotein lipase gemfibrozil and clofibrate
two drugs that act as bile acid sequestrants cholestyramine and colestipol
aminocaproic acid is indicated for : control of bleeding by hyperfibrinolysis, and prophylaxis in
hemophiliacs undergoing a surgical procedure
what causes hemolysis in G6PD deficient individuals? oxidative stress (low NADPH means glutathione
cannot scavenge free radicals)
1st-line rx for panic disorder SSRI
reserved for refractory cases of schizophrenia due to risk of agranylocytosis clozapine
inappropriate laughter, scleral injection, tachycardia, and paranoia are typical of a person using what
illicit substance? cannabis
1st-line rx for DVT IV heparin
1st-line rx for hypothyroidism levothyroxine
contraindication for levothyroxine use CAD (enhances β-adrenergic effects; may precipitate MI)
toxicities of methotrexate liver, renal, BM
after CLL chemotherapy, patients are at risk for what type of kidney stones? uric acid
alcoholics have (increased/decreased) levels of theophylline decreased (EtOH induces P450)
name the K+ sparing diuretics spironolactone, triamterene, amiloride
drug class of salsalate NSAID (salicylate)
effect of ammonium chloride on the urine acidifies
interaction of ammonium chloride and salicylates salicylate toxicity (amm chloride inhibits excretion)
mechanism of flutamide comp antagonist at androgen receptors
mechanism of finasteride 5- α reductase inhibitor
Class I antiarrhythmics block ___ sodium channels
Name some class I antiarrhythmics quinidine (A), amiodarone (A, III), procainamide (A), lidocaine (B),
flecainide ©
Class II antiarrhythmics block ___ beta-adrenergic receptors
Class III antiarrhythmics block ____ potassium channels
Name some class III antiarrhythmics sotalol (also β), amiodarone, bretylium
Class IV antiarrhythmics block ___ calcium channels
Name some class IV antiarrhythmics verapamil, diltiazam
mechanism of metoclopromide antagonist at D receptors
use of metoclopromide prokinetic agent used in GERD and diabetic gastroparesis
contraindication for metoclopromide (2) bowel obstruction, Parkinson's
necrosis of the skin can be a toxicity of what anticoagulant? warfarin
drug given for acute gouty attacks colchicine
xanthine oxidase inhibitor used in gout allpurinol
increases the excretion of uric acid (2) probenacid, sulfinpyrazone
define REM rebound some drugs steal REM; when removed, body has more REM, including vivid dreams
drugs that cause REM rebound when withdrawn barbiturates, EtOH, MAOI, phenothiazines
mechanism of caffeine inhibition of phosphodiesterase (prevent cAMP degradation)
carbonic anhydrase inhibitors can lead to what acid-base disturbance? metabolic acidosis
close a PDA with : indomethacin
class of drugs that must be given to a patient in a fib and WHY anticoagulants; because the flow in the
atrium is nonlaminar and predisposes to mural clots
inhaled corticosteroids are associated with ___ in asthmatic patients (microbial infxn) candidiasis
these cardiac drugs "mask" the initial sx of hypoglycemia and are thus contraindicated in diabetics β
blockers
analgesic of choice for acute cholecystitis and WHY meperidine; least likely to cause spasm of sphincter
of Oddi
initial drug of choice for acute status epilepticus diazepam
indications for carbamazepine prophylaxis and treatment of tonic-clonic, focal, and complex partial
seizures
drug of choice for absence seizures ethosuximide
NSAID that is contraindicated in patients with sulfa allergy celecoxib
location of action of spironolactone collecting tubule
Name some drugs associated with the development of SIADH tricyclics, carbamazepine, SSRI, MAOI,
neuroleptics, antineoplastics
post-MI drugs that cause dry cough ACE-I (captopril, enalapril)
two β1-selective antagonists metoprolol and atenolol. Atenolol is a beta1-selective (cardioselective)
beta-adrenergic receptor blocking agent.
Metoprolol - Clinical Pharmacology
Metoprolol tartrate is a beta-adrenergic receptor blocking agent. In vitro and in vivo animal studies have
shown that it has a preferential effect on beta1 adrenoreceptors, chiefly located in cardiac muscle. This
preferential effect is not absolute, however, and at higher doses, Metoprolol also inhibits beta2
adrenoreceptors, chiefly located in the bronchial and vascular musculature.
Clinical pharmacology studies have confirmed the beta-blocking activity of Metoprolol in man, as shown
by (1) reduction in heart rate and cardiac output at rest and upon exercise, (2) reduction of systolic
blood pressure upon exercise, (3) inhibition of isoproterenol-induced tachycardia, and (4) reduction of
reflex orthostatic tachycardia.
Relative beta1 selectivity has been confirmed by the following: (1) In normal subjects, Metoprolol is
unable to reverse the beta2-mediated vasodilating effects of epinephrine. This contrasts with the effect
of nonselective (beta1 plus beta2) beta blockers, which completely reverse the vasodilating effects of
epinephrine. (2) In asthmatic patients, Metoprolol reduces FEV1 and FVC significantly less than a
nonselective beta blocker, propranolol, at equivalent beta1-receptor blocking doses.
Metoprolol has no intrinsic sympathomimetic activity, and membrane-stabilizing activity is detectable
only at doses much greater than required for beta blockade. Metoprolol crosses the blood-brain barrier
and has been reported in the CSF in a concentration 78% of the simultaneous plasma concentration.
Animal and human experiments indicate that Metoprolol slows the sinus rate and decreases AV nodal
conduction.
In controlled clinical studies, Metoprolol tartrate has been shown to be an effective antihypertensive
agent when used alone or as concomitant therapy with thiazide-type diuretics, at dosages of 100 to 450
mg daily. In controlled, comparative, clinical studies, Metoprolol has been shown to be as effective an
antihypertensive agent as propranolol, methyldopa, and thiazide-type diuretics, and to be equally
effective in supine and standing positions.
The mechanism of the antihypertensive effects of beta-blocking agents has not been elucidated.
However, several possible mechanisms have been proposed: (1) competitive antagonism of
catecholamines at peripheral (especially cardiac) adrenergic neuron sites, leading to decreased cardiac
output; (2) a central effect leading to reduced sympathetic outflow to the periphery; and (3) suppression
of renin activity.
By blocking catecholamine-induced increases in heart rate, in velocity and extent of myocardial
contraction, and in blood pressure, Metoprolol reduces the oxygen requirements of the heart at any
given level of effort, thus making it useful in the long-term management of angina pectoris. However, in
patients with heart failure, beta-adrenergic blockade may increase oxygen requirements by increasing
left ventricular fiber length and end-diastolic pressure.
Although beta-adrenergic receptor blockade is useful in the treatment of angina and hypertension,
there are situations in which sympathetic stimulation is vital. In patients with severely damaged hearts,
adequate ventricular function may depend on sympathetic drive. In the presence of AV block, beta
blockade may prevent the necessary facilitating effect of sympathetic activity on conduction. Beta2-
adrenergic blockade results in passive bronchial constriction by interfering with endogenous adrenergic
bronchodilator activity in patients subject to bronchospasm and may also interfere with exogenous
bronchodilators in such patients.