| Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | Pravastatin Na 
 Dosage forms
 |  | Definition 
 
        | Tablets:  10, 20, 40, and 80 mg |  | 
        |  | 
        
        | Term 
 
        | Pravastatin Na    FDA indications/Dosages |  | Definition 
 
        | 1.  Primary hyper-cholesterolemia & mixed dyslipidemia (Fredrickson types IIa & IIb):  After 3-6 wks cholesterol-lowering diet, start 10-20 mg HS.  Adjust q4wks up to max 40 mg QD   2.  MI, coronary death, & myocardial revascularization procedures:  Start 10-20 mg HS.  Adjust q4wks up to max 40 mg QD   3.  8-18 y/o w/ heterozygous familial hypercholesterolemia:  <13 y/o-20 mg QPM.  14-18 y/o 40 mg QPM |  | 
        |  | 
        
        | Term 
 
        | Pravastatin Na 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 
        | inhibitor of HMG-CoA reductase |  | 
        |  | 
        
        | Term 
 
        | Pravastatin Na 
 Drug interactions
 |  | Definition 
 
        | 1.  Gemfibrozil, Nicotinic acid, Erthromycin, or Immunosuppressive agents - rhabdo or myopathy 
 2.  Cholestyramine & colestipol increases effects.  Give pravastatin 1 hr before or 4 hrs after these meds.
 |  | 
        |  | 
        
        | Term 
 
        | Pravastatin Na 
 CIs/Precautions
 |  | Definition 
 
        | 1.  Pregnancy or lactation 2.  active liver disease
 3.  unexplained persistant elevations of serum transaminases
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Rash, Muscle pain, HA, Influenza, dyspepsia |  | 
        |  | 
        
        | Term 
 
        | Pravastatin Na  Pt consultation |  | Definition 
 
        | 1.  Warn about myopathy 2.  Avoid sunlight 3.  If pregnant, DC 4.  Limit OH |  | 
        |  | 
        
        | Term 
 
        | Estrogen (conjugated) 
 Brand Name
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Estrogen (conjugated) 
 Dosage forms
 |  | Definition 
 
        | Tablets:  0.3, 0.45, 0.625, 0.9, and 1.25 Vaginal cream:  0.625 mg/1g
 IV:  25 mg per Secule
 
 Available in a formulation w/ methyltestosterone
 |  | 
        |  | 
        
        | Term 
 
        | Estrogen (conjugated)  FDA indications/Dosages |  | Definition 
 
        | Oral dosage 1.  Vasomotor sxs associated w/ menopause 2.  Female hypogonadism 3.  Female castration & primary ovarian failure 4.  Breast cancer 5.  prostatic carcinoma 6.  Prevention of postmenopausal osteoporosis after other non-estrogen txs have been considered   IV 1.  Abnormal uterine bleeding due to hormonal imbalance in the absence of organic pathology   Cream 1.  Atrophic vaginitis & krauosis vulvae 2.  Tx of moderate to severe dyspareunia due to menopause |  | 
        |  | 
        
        | Term 
 
        | Estrogen (conjugated)  Pharmacology/Pharmacokinetics |  | Definition 
 
        | Estrogens decrease the release of FSH, LH, and luteotropic hormone due to an effect on the pituitary or hypothalamus |  | 
        |  | 
        
        | Term 
 
        | Estrogen (conjugated) 
 Drug interactions
 |  | Definition 
 
        | 1.  Barbiturates, rifampin, &/or hydantoins increase metabolism & elimination 
 2.  Increase toxic effects of corticosteroids
 |  | 
        |  | 
        
        | Term 
 
        | Estrogen (conjugated)  CIs/Precautions |  | Definition 
 
        | 1.  suspected breast cancer 2.  suspected estrogen-dependent neoplasia 3.  pregnancy 4.  undx abnormal genital bleeding 5.  thrombophlebitis, thrombosis, or thromboembolic disorders except when used in tx of breast or prostatic malignancy 6.  nursing mothers |  | 
        |  | 
        
        | Term 
 
        | Estrogen (conjugated) 
 ADEs
 |  | Definition 
 
        | Rash, acne, alopecia, hirsutism, abnormal menstrual bleeding |  | 
        |  | 
        
        | Term 
 
        | Estrogen (conjugated)  Pt consultation |  | Definition 
 
        | 1.  May be taken w/ food or milk if GI upset occurs 2.  Read pt info sheet carefully 3.  DC if suspected pregnancy 4.  Report to MD if pains in the legs, coughing blood, abnormal vaginal bleeding, skin yellowing, and abdominal pain |  | 
        |  | 
        
        | Term 
 
        | Isosorbide Mononitrate 
 Brand Name
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Isosorbide Mononitrate 
 Dosage forms
 |  | Definition 
 
        | Tablets ER:  30, 60, and 120 mg |  | 
        |  | 
        
        | Term 
 
        | Isosorbide Mononitrate 
 FDA indications/Dosages
 |  | Definition 
 
        | Prophylatic tx of angina pectoris due to CAD 
 Normal daily dose:  30-120 mg QAM
 Starting dose:  30-60 mg QAM
 Several days:  120 mg
 Max daily dose:  240 mg
 
 Each dose should be followed by 4 oz of fluid
 |  | 
        |  | 
        
        | Term 
 
        | Isosorbide Mononitrate 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 
        | Reduction of myocardial oxygen demand thru the relaxation of vascular smooth muscle |  | 
        |  | 
        
        | Term 
 
        | Isosorbide Mononitrate 
 Drug interactions
 |  | Definition 
 
        | 1.  OH - hypotensive effects 2.  vasodilators (CCBs)- additive effects
 |  | 
        |  | 
        
        | Term 
 
        | Isosorbide Mononitrate  CIs/Precautions |  | Definition 
 
        | 1.  Hypersensitive to nitrates 2.  during the acute phase of MI 3.  CHF |  | 
        |  | 
        
        | Term 
 
        | Isosorbide Mononitrate 
 ADEs
 |  | Definition 
 
        | HA, dizziness, rash, cutaneous vasodilation |  | 
        |  | 
        
        | Term 
 
        | Isosorbide Mononitrate 
 Pt consultation
 |  | Definition 
 
        | HAs are a sign of effectiveness and avoid OH |  | 
        |  | 
        
        | Term 
 
        | Triamterene w/ HCTZ 
 Brand Name
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Triamterene w/ HCTZ 
 Dosage forms
 |  | Definition 
 
        | Capsules (Dyazide):  37.5/25 Tablets (Maxzide-25):  37.5/25
 Tablets (Maxzide):  75/50
 |  | 
        |  | 
        
        | Term 
 
        | Triamterene w/ HCTZ 
 FDA indications/Dosages
 |  | Definition 
 
        | 1.  Adjunctive therapy in edema associated with CHF, hepatic cirrhosis, nephrotic syndrome, & in corticosteroid & estrogen:  1-2 doses BID 
 2.  Management of HTN:  1-2 doses a day
 
 some may require 1 dose or EOD
 |  | 
        |  | 
        
        | Term 
 
        | Triamterene w/ HCTZ  Pharmacology/Pharmacokinetics |  | Definition 
 
        | Triamterene inhibits the reabsorption of Na in exchange for K at the DCT   HCTZ inhibits the reabsorption of Na & Cl at the DCT     |  | 
        |  | 
        
        | Term 
 
        | Triamterene w/ HCTZ 
 Drug interactions
 |  | Definition 
 
        | 1.  Toxic effects of cardiac glycoside, diazoxide, & Li may be increased 
 2.  HyperK w/ K-sparing diuretics, K supplements, & ACEI
 
 3.  Effects of sulfonylureas may be decreased
 |  | 
        |  | 
        
        | Term 
 
        | Triamterene w/ HCTZ 
 CIs/Precautions
 |  | Definition 
 
        | 1.  anuria 2.  hyperK
 3.  hypersensitivity to sulfonamide-derived drugs
 4.  K-sparing diuretics
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Dry mouth, muscle cramps, N, V |  | 
        |  | 
        
        | Term 
 
        | Triamterene w/ HCTZ 
 Pt consultation
 |  | Definition 
 
        | 1.  Diuresis should be given in early AM 2.  Avoid sunlight
 |  | 
        |  | 
        
        | Term 
 
        | Insulin Aspart, rDNA origin 
 Brand Name
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Insulin Aspart, rDNA origin 
 Dosage forms
 |  | Definition 
 
        | Novolog:  100 u/mL Novolog Mix 70/30:  30% insulin aspart soln & 70% insulin aspart protamine suspension
 |  | 
        |  | 
        
        | Term 
 
        | Insulin Aspart, rDNA origin 
 FDA indications/Dosages
 |  | Definition 
 
        | TIDM or T2DM:  Dose is individualized.  Give w/in 5-10 min to a meal.  Protamine suspension has a longer DOA than insulin aspartate |  | 
        |  | 
        
        | Term 
 
        | Insulin Aspart, rDNA origin 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 
        | Promotes the transport of monsaccharides across cell membranes and facilitates the transformation of intracellular aas into ptns. 
 Decreases the formation of TGs
 |  | 
        |  | 
        
        | Term 
 
        | Insulin Aspart, rDNA origin 
 Drug interactions
 |  | Definition 
 
        | 1.  Corticosteroids, diltizem, dobutamine, epinephrine, OC, thiazide diuretics, thyroid, & tobacco smoke - decrease the effects 
 2.  OH, anabolic steroids, BBs, clofibrate, fenfluramine, guanethidine, MAO-Is, phenylbutazone, salicylates, sulfinpyrazone, & TET - increase the effects
 |  | 
        |  | 
        
        | Term 
 
        | Insulin Aspart, rDNA origin 
 CIs/Precautions
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Insulin Aspart, rDNA origin 
 ADEs
 |  | Definition 
 
        | Hypoglycemia, hypersensitivity |  | 
        |  | 
        
        | Term 
 
        | Insulin Aspart, rDNA origin 
 Pt consultation
 |  | Definition 
 
        | 1.  Administer 5-10 min before meals 2.  Do not change syringe brands or dose w/o first notifying the MD
 3.  Monitor blood or urine glucose as prescribed
 4.  Carry diabetic ID in case of emergency
 5.  Store in refrigerator
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | Memantine HCl 
 Dosage forms
 |  | Definition 
 
        | Tablets:  5 and 10 mg Oral Soln:  2 mg/mL (OH-free, sugar-free, peppermint flavor)
 |  | 
        |  | 
        
        | Term 
 
        | Memantine HCl  FDA indications/Dosages |  | Definition 
 
        | dementia of Alzheimer's type: Starting dose 5 mg QD x 1 wk Increase 5 mg BID x 1 wk Increase 5 mg in AM & 10 mg in PM x 1 wk Increase dose to 10 mg BID Target dose:  20 mg QD |  | 
        |  | 
        
        | Term 
 
        | Memantine HCl  Pharmacology/Pharmacokinetics |  | Definition 
 
        | activation of NMDA receptors by the excitatory aa glutamate |  | 
        |  | 
        
        | Term 
 
        | Memantine HCl 
 Drug interactions
 |  | Definition 
 
        | CAIs or Na bicarbonate (alkalinize the urine) reduce the renal elimination of drug |  | 
        |  | 
        
        | Term 
 
        | Memantine HCl 
 CIs/Precautions
 |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Dizziness, HA, confusion, HTN, pain |  | 
        |  | 
        
        | Term 
 
        | Memantine HCl  Pt consultation |  | Definition 
 
        | May be taken with or without food |  | 
        |  | 
        
        | Term 
 
        | Hydroxyzine HCl 
 Brand Name
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Hydroxyzine HCl 
 Dosage forms
 |  | Definition 
 
        | Tablets:  10, 25, and 50 mg Syrup:  10 mg/5 mL (OH 0.5%)
 Injection:  25 mg/mL and 50 mg/mL in ampules & multi-dose vials
 |  | 
        |  | 
        
        | Term 
 
        | Hydroxyzine HCl  FDA indications/Dosages |  | Definition 
 
        | 1.  Symptomatic relief of anxiety & tension associated w/ psychoneurosis & as an adjunct in organic disease states in which anxiety is manifested:   Adults:  50-100 mg QID >6 y/o:  50-100 mg in divided doses <6 y/o:  50 mg in divided doses   2.  Managementof pruritus due to allergic conditions such as chronic urticaria, atopic dermatoses, & contact dermatoses and in histamine-mediated pruritus   Adults:  25 mg TID-QID >6 y/o:  50-100 mg in divided doses <6 y/o:  50 mg daily in divided doses   3.  sedative when used as a premedication and following general anesthesia   50-100 mg for adults 0.6 mg/kg for children |  | 
        |  | 
        
        | Term 
 
        | Hydroxyzine HCl 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Hydroxyzine HCl 
 Drug interactions
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Hydroxyzine HCl 
 CIs/Precautions
 |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | Hydroxyzine HCl 
 Pt consultation
 |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | Paroxetine HCl 
 Dosage forms
 |  | Definition 
 
        | Tablets:  10, 20, 30, and 40 mg Tablets, CR:  12.5, 25, and 37.5 mg
 Oral suspension:  10 mg/5 mL (orange-flavored)
 |  | 
        |  | 
        
        | Term 
 
        | Paroxetine HCl 
 FDA indications/Dosages
 |  | Definition 
 
        | Paxil- 1.  Depression & OCD
 2.  Depression in elderly or debilitated or pts w/ severe renal or hepatic impairment
 3.  Panic disorder
 4.  SAD
 
 Paxil CR-
 1.  Depression
 2.  Panic disorder
 3.  Premenstrual dysphoric disorder
 |  | 
        |  | 
        
        | Term 
 
        | Paroxetine HCl  Pharmacology/Pharmacokinetics |  | Definition 
 
        | selective inhibitor of neuronal 5HT   weak inhibitor of NE & DA |  | 
        |  | 
        
        | Term 
 
        | Paroxetine HCl  Drug interaction |  | Definition 
 
        | 1.  MAO-Is 2.  drug may be increased or decreased when used w/ phenytoin, phenobarbital, or cimetidine 3.  displace Warfarin 4.  increase levels of procyclidine 5.  Variables effects w/ 2D6 6.  ASA or NSAID - increase upper GI bleeding |  | 
        |  | 
        
        | Term 
 
        | Paroxetine HCl 
 CIs/Precautions
 |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | nausea, somnolence, HA, asthenia, sexual dysfx |  | 
        |  | 
        
        | Term 
 
        | Paroxetine HCl 
 Pt consultation
 |  | Definition 
 
        | drowsiness 
 avoid OH
 
 2 weeks to see effects
 
 No DC
 
 Do not take sooner than q24h
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Tablets:  15, 30, and 45 mg ODTs:  15, 30, and 45 mg
 |  | 
        |  | 
        
        | Term 
 
        | Mirtazapine 
 FDA indications/Dosages
 |  | Definition 
 
        | Depression:  starting-15 mg HS; maintenance-15-45 mg QD 
 Dosage changes should occur at intervals of 1-2 weeks
 |  | 
        |  | 
        
        | Term 
 
        | Mirtazapine  Pharmacology/Pharmacokinetics |  | Definition 
 
        | antagonist of central presynaptic alpha-2 adrenergic inhibitory autoreceptors & heteroreceptors, an action that is postulated to result in an increase in central noradrenergic and serotonergic activity |  | 
        |  | 
        
        | Term 
 
        | Mirtazapine  Drug interactions |  | Definition 
 
        | 1.  CNS depressants 2.  MAO-Is 3.  ASA or NSAID |  | 
        |  | 
        
        | Term 
 
        | Mirtazapine  CIs/Precautions |  | Definition 
 
        | 1.  MAOI in 14 days 2.  sore throat, fever, stomatitis, or other signs of infection, along w/ a low WBC count |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Drowsiness, dry mouth, increased appetite, constipation |  | 
        |  | 
        
        | Term 
 
        | Mirtazapine 
 Pt consultation
 |  | Definition 
 
        | Drowsiness 
 Avoid OH
 
 No DC
 
 SolTabs must be used immediately upon opening individual tablet blisters
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Tablets:  40, 80, 160, and 320 mg |  | 
        |  | 
        
        | Term 
 
        | Valsartan 
 FDA indications/Dosages
 |  | Definition 
 
        | 1.  Tx of HTN when used alone or in combo w/ other anti-HTN: 
 Starting dose-80 mg QD in pts who are not V-depleted
 Maintenance dose-80-320 mg QD
 
 2.  Tx of HF (NYHA II-IV) in pts who are intolerant of ACEIs:  Starting dose-40 mg BID.  Titration 80 mg & 160 mg BID
 
 3.  CV mortality following MI in pts w/ ventricular failure or dysfx:  Start 20 mg BID.  Uptitrate to 160 mg BID
 |  | 
        |  | 
        
        | Term 
 
        | Valsartan  Pharmacology/Pharmacokinetics |  | Definition 
 
        | It blocks the vasoconstrictor & aldosterone-secreting effects of Ang II by selectively blocking the binding of ang II to the AT1 receptor |  | 
        |  | 
        
        | Term 
 
        | Valsartan  Drug interactions |  | Definition 
 
        | NSAIDs may decrease the effects and increase reisk of renal function of deterioration |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | Valsartan  Pt consultation |  | Definition 
 
        | 1.  May be taken w/ or w/o food, although it may be best to administer Diovan w/o food for consistent plasma level 2.  If pregnant, DC 3.  Dizziness may occur the 1st few days |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Capsules:  50, 100, 200, and 400 mg |  | 
        |  | 
        
        | Term 
 
        | Celecoxib 
 FDA indications/Dosages
 |  | Definition 
 
        | 1.  Relief of the signs & sxs of OA:  200 mg QD or 100 mg BID 
 2.  Relief of sixns & sxs of RA in adults:  100-200 mg BID
 
 3.  Management of acute pain & dysmenorrhea:
 400 mg in a single dose, followed by a 200 mg dose PRN
 Maintenance-200 mg BID
 
 4.  Reduce the # of adenomatous coloretal polyps in familial adenomatous polyposis (FAP), as an adjunct to usual care:  400 mg BID WF
 
 5.  Relieve the signs & sxs of ankylosing spondylitis:  200 mg QD or BID
 |  | 
        |  | 
        
        | Term 
 
        | Celecoxib 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 
        | Produces its anti-inflammatory, analgesic, & antipyretic effects by inhibiting PG synthesis thru inhibition of COX-2 |  | 
        |  | 
        
        | Term 
 
        | Celecoxib  Drug interactions |  | Definition 
 
        | 1.  decrease the effects of ACEIs 2.  increase Li levels 3.  Fluconazole increases plasma levels 4.  inhibitor of 2C9 5.  increase effects of warfarin |  | 
        |  | 
        
        | Term 
 
        | Celecoxib  CIs/Precautions |  | Definition 
 
        | 1.  asthma, urticaria, or allergic-type rxs after taking sulfonamides, ASA, or NSAIDs 2.  peri-operative pain in the setting of coronary artery bypass graft surgery |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | D, dyspepsia, abd pain, flatulence, edema, & sinusitis |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Report any signs of ulcerations & bleeding to MD 
 Avoid ASA
 |  | 
        |  | 
        
        | Term 
 
        | Nitroglycerin (SL & injectable) 
 Brand Name
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Nitroglycerin (SL & injectable) 
 Dosage forms
 |  | Definition 
 
        | Tablets SL:  0.3, 0.4, and 0.6 mg Injection:  5 mg/mL
 |  | 
        |  | 
        
        | Term 
 
        | Nitroglycerin (SL & injectable) FDA indications/Dosages |  | Definition 
 
        | 1.  Prophylaxis, tx, & management of angina pectoris (SL): Dissolve 1 TA under the tongue or in the buccal pouch at first sign of an acute anginal attack  Use no more >3 tablets in 15 minutes   2.  Tx of angina pectoris, perioperative HTN, CHF associated w/ MI, & for production of controlled hypotension during surgery: Must be individualized  Diluted prior to use.  Start w/ 5 mcg/min & titrate to the optimum response using 5 mcg/min increments w/ q 3-5 min until some response is seen.   Increments of 10-20 mcg/min may be used if no response is seen at 20 mcg/min |  | 
        |  | 
        
        | Term 
 
        | Nitroglycerin (SL & injectable) 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 
        | Reduction of myocardial oxygen demand thru the relaxation of vascular smooth muscle is the primary pharmacological effect of nitrates |  | 
        |  | 
        
        | Term 
 
        | Nitroglycerin (SL & injectable)  Drug interactions |  | Definition 
 
        | 1.  Dihydroergotamine may be increased 2.  Heparin may be decreased 3.  Hypotensive effects may be increased by sildenafil citrate |  | 
        |  | 
        
        | Term 
 
        | Nitroglycerin (SL & injectable)  CIs/Precautions |  | Definition 
 
        | 1.  intoleratnt to organic nitrates  2.  severe anemias 3.  closed-angle glaucoma 4.  postural hypotension 5.  increased intracranial pressure 6.  early MI 7.   injection in pts w/ hypotension or uncorrected hypovolemia 8.  injection in pts w/ constrictive pericarditis or pericardial tamponade |  | 
        |  | 
        
        | Term 
 
        | Nitroglycerin (SL & injectable) 
 ADEs
 |  | Definition 
 
        | transient HA, N, V, D, flushing of face or neck, and rapid pulse |  | 
        |  | 
        
        | Term 
 
        | Nitroglycerin (SL & injectable) 
 Pt consultation
 |  | Definition 
 
        | Store in a glass or metal container 
 OH may aggravate angina
 
 Sit down when taking SL NG tablets to avoid lightheadedness & fainting
 
 Dispense tablets in original container (glass) & counsel  on keeping them in the original container (to avoid leaching).  Close tightly
 
 Taste bitter
 
 Dissolve tablet under the tongue
 
 After placing 1st tablet under the tongue, if angina is not relieved in 5 min, dissolve a 2nd tablet under the tongue & then a 3rd tablet if necessary
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Capsules DR:  15 and 30 mg ODTs:  15 and 30 mg
 Granules DR oral suspension:  15 and 30 mg
 Powder for injection:  Each vial contains 30 mg
 |  | 
        |  | 
        
        | Term 
 
        | Lansoprazole 
 FDA indications/Dosages
 |  | Definition 
 
        | 1.  Short-term tx of active duodenal ulcer 2.  Tx of duodenal ucler associated w/ H. pylori
 3.  Short-term tx of gastric ulcers
 4.  Short-term tx of erosive esophagitis
 5.  Maintain the healing of erosive esophagitis & gastic ulcers
 6.  Tx of GERD in pts >1 y/o
 7.  Zollinger-Ellision syndrome
 8.  Nasogastric tubes
 |  | 
        |  | 
        
        | Term 
 
        | Lansoprazole 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 
        | Inhibits the H+/K+ ATPase enzyme system at the secretory surface of the gastric parietal cell |  | 
        |  | 
        
        | Term 
 
        | Lansoprazole 
 Drug interactions
 |  | Definition 
 
        | 1.  30 min prior to sucralfate 2.  Gastric pH effects Ketoconazole, AMP esters, Fe salts, digoxin
 3.  Titration of theophylline dosage
 |  | 
        |  | 
        
        | Term 
 
        | Lansoprazole 
 CIs/Precautions
 |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Diarrhea, abd pain, N, and HA |  | 
        |  | 
        
        | Term 
 
        | Lansoprazole 
 Pt consultation
 |  | Definition 
 
        | Take on an empty stomach 
 Mix granules w/ 30 mL of water, stir well & drink immediately.  If granules remain after drinking, add more water, stir and drink immediately.
 
 IV must be reconstituted according to the manufacturer's directions and administered using an in-line filter
 |  | 
        |  | 
        
        | Term 
 
        | Doxycycline Hyclate 
 Brand Name
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Doxycycline Hyclate  Dosage forms |  | Definition 
 
        | Tablets:  100 mg Capsules:  50 and 100 mg Syrup:  50 mg/5 mL (Ca salt) raspberry/apple-flavored suspension Powder for Oral suspension:  25 mg as monohydrate/5 mL after reconstitution, raspberry flavor Powder for injection:  100 and 200 mg/vial |  | 
        |  | 
        
        | Term 
 
        | Doxycycline Hyclate 
 FDA indications/Dosages
 |  | Definition 
 
        | 1.  Infections due to susceptible strains of gram -/+ bacilli & cocci, spirochetes.  M. pneumoniae, actinomycetes, & rickettsiae 2.  Primary & secondary syphilis
 3.  Uncomplicated gonorrhea
 4.  Uncomplicated urethral, endocervical, or rectal infections due to Chlamydia trachomatis
 5.  Prophylaxis of malaria due to Plasmodium falciparum in short-term travelers to areas w/ strains resistant to other therapy
 6.  >8 y/o
 |  | 
        |  | 
        
        | Term 
 
        | Doxycycline Hyclate 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 
        | Prevents ptn synthesis by competitively bindin to the 30S ribosomal subunit |  | 
        |  | 
        
        | Term 
 
        | Doxycycline Hyclate 
 Drug interactions
 |  | Definition 
 
        | 1.  Bactericidal antibiotics 2.  OCs
 3.  Increase the bioavailabiity of digoxin
 4.  Absorption impaired by Al, bismuth, Ca, Mg, Zn, and Fe salts, & urinary alkalinizers
 5.  Methoxyflurane - nephrotoxicity
 |  | 
        |  | 
        
        | Term 
 
        | Doxycycline Hyclate 
 CIs/Precautions
 |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Dizziness, vertigo, nausea, vomiting, D, increased sensitivity to sunligh, discoloration of forming teeth, sore, or darkened tongue, cramps, & burning stomach |  | 
        |  | 
        
        | Term 
 
        | Doxycycline Hyclate 
 Pt consultation
 |  | Definition 
 
        | 1.  1 hr before or 2 hrs after meals w/ a full glass 8oz 2.  Take at even intervals
 3.  Complete full course
 4.  Avoid sunlight
 5.  shake suspension
 |  | 
        |  | 
        
        | Term 
 
        | Amphetamine w/ Dextroamphetamine salts 
 Brand Name
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Amphetamine w/ Dextroamphetamine salts 
 Dosage forms
 |  | Definition 
 
        | Tablets:  5, 7.5, 10, 12.5, 15, 20, and 30 mg Capsules ER:  5, 10, 15, 20, 25, and 30 mg
 |  | 
        |  | 
        
        | Term 
 
        | Amphetamine w/ Dextroamphetamine salts  FDA indications/Dosages |  | Definition 
 
        | 1.  Narcolepsy:  5-60 mg/day in divided doses   2.  ADD w/ hyperactivity   3-5 y/o:  2.5 mg QD & increase by 2.5 mg at weekly intervals until optimum effects >5 y/o:  5-10 mg QD & increase by 5 mg weekly intervals until optimum effect   Adults (XR):  20 mg/day |  | 
        |  | 
        
        | Term 
 
        | Amphetamine w/ Dextroamphetamine salts 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 
        | Direct action on adrenergic receptors releasing NE from storage sites |  | 
        |  | 
        
        | Term 
 
        | Amphetamine w/ Dextroamphetamine salts  Drug interactions |  | Definition 
 
        | 1.  MAO-I and furazolidone increase the effects 2.  Urine alkalinizing agents (Na bicarbonate) increase reabsorption while GI alkalinizing agents increase absorption 3.  Decrease effects anti-HTN |  | 
        |  | 
        
        | Term 
 
        | Amphetamine w/ Dextroamphetamine salts  CIs/Precautions |  | Definition 
 
        | 1.  ateriosclerosis 2.  CVD 3.  moderate HTN 4.  hyperthyroidism 5.  agitated states 6.  glaucoma 7.  MAO-I w/in 14 days 8.  Drug abuse |  | 
        |  | 
        
        | Term 
 
        | Amphetamine w/ Dextroamphetamine salts 
 ADEs
 |  | Definition 
 
        | Restlessness, dizziness, insomnia, euphoria, tremor, HA |  | 
        |  | 
        
        | Term 
 
        | Amphetamine w/ Dextroamphetamine salts 
 Pt consultation
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Fentanyl (Transdermal) 
 Brand Name
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Fentanyl (Transdermal) 
 Dosage forms
 |  | Definition 
 
        | Transdermal systems: 12 (12.5) mcg/h in 5 cm^2 (contains 1.25 mg fentanyl)
 
 25 mcg/h in 10 cm^2 (contains 2.5 mg fentanyl)
 
 
 50 mcg/h in 20 cm^2 (contains 5.0 mg fentanyl)
 
 
 75 mcg/h in 30 cm^2 (contains 7.5 mg fentanyl)
 
 100 mcg/h in 40 cm^2 (contains 10.0 mg fentanyl)
 |  | 
        |  | 
        
        | Term 
 
        | Fentanyl (Transdermal) 
 FDA indications/Dosages
 |  | Definition 
 
        | 1.  Management of chronic pain in pts requiring opioid analgesia 2.  conversion from oral or parenteralopioids to fentanyl use the following methodology
 3.  short acting analgesics for the 1st 24 hours PRN until analgesic efficacy w/ duragesic is attained
 |  | 
        |  | 
        
        | Term 
 
        | Fentanyl (Transdermal) 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Fentanyl (Transdermal)  Drug interactions |  | Definition 
 
        | Additive CNS depression w/ phenothiazines, general anesthetics, sedatives, hypnotics OH, skeletal muscle relaxants, & agonist/antagonist analgesics |  | 
        |  | 
        
        | Term 
 
        | Fentanyl (Transdermal) 
 CIs/Precautions
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Fentanyl (Transdermal) 
 ADEs
 |  | Definition 
 
        | Hypoventilation, hypotension, HTN, abd pain, HA, N, V, constipation |  | 
        |  | 
        
        | Term 
 
        | Fentanyl (Transdermal) 
 Pt consultation
 |  | Definition 
 
        | 1.  Press down 10-20 seconds 2.  Worn continuously for 72 h
 3.  Do not cut or puncture systems
 4.  Report to MD if any diffculty breathing
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | Ezetimibe  FDA indications/Dosages |  | Definition 
 
        | 1.  familial or nonfamilial hypercholesterolemia 2.  combo w/ HMG-CoA reductase inhibitor w/ familial or nonfamilial hypercholesterolemia 3.  combo w/ Lipitor or Zocor w/ homozygous familial hypercholesterolemia as an adjunct to othe rlipid-lowering txs apheresis or if such txs are unavailable 4.  adjunctive therapy to diet for the reduction of elevated sitosterol & campesterol levels w/ homozygous familial sitosterolemia 5.  combo w/ fenofibrate  for mixed hyperlipidemia   10 mg |  | 
        |  | 
        
        | Term 
 
        | Ezetimibe 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 
        | inhibits the intestinal absorption of cholesterol & related phytosterols |  | 
        |  | 
        
        | Term 
 
        | Ezetimibe 
 Drug interactions
 |  | Definition 
 
        | 1.  Gemfibrozil & fenofibrate increase plasma [ ] 2.  Cholestyramine decreases plasma [ ]
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | 1.  Hypersensitivity 2.  moderate to severe hepatic insufficiency
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Myalgia, increased CPK, elevations in liver transaminases, hepatitis, thrombocytopenica |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Do not take w/in 2 h before or 4 h after the administration of cholestyramine |  | 
        |  | 
        
        | Term 
 
        | Ciprofloxacin HCl 
 Brand Name
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Ciprofloxacin HCl  Dosage forms |  | Definition 
 
        | Tablets (Cystitis Pak):  100, 250, 500, and 750 mg Tablets ER (Cipro XR):  500 and 1000 mg Oral suspension:  100 mL containing either 5% or 10% Injection: 200 mg in 20 mL vials (1%) and 100 mL in 5% dextrose (0.2%). 400 mg in 40 mL vials (1%) and 200 mL in 5% dextrose  (0.2%) |  | 
        |  | 
        
        | Term 
 
        | Ciprofloxacin HCl 
 FDA indications/Dosages
 |  | Definition 
 
        | 1.  Infectious D caused by E. coli, C. jejuni, s. flexneri, or S. sonnei 2.  UTIs
 3.  acute uncomplicated pyelonephritis
 4.  lower respiratory tract, skin & skin structure, & bone and joint infections caused by aforementioned bacteria
 5.  Thphoid fever
 6.  uncomplicated cervical & urethral gonorrhea
 7.  acute uncomplicated cystitis in females
 8.  complicated intra-abd infections used in combo w/ flagyl
 9.  bone/joint infections
 10.  reduce the incidence or progression of disease following exposure to aerosolized
 11.  impaired renal fx
 |  | 
        |  | 
        
        | Term 
 
        | Ciprofloxacin HCl 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Ciprofloxacin HCl  Drug interactions |  | Definition 
 
        | 1.  Antacaids and Fe salts decrease bioavailability 2.  Probenecid increases serum levels by decreasing excretion 3.  NSAIDs lower seizure thresholds 4.  predispose pts to convulsive seizures when taking w/ levofloxacin 5.  increase theophylline |  | 
        |  | 
        
        | Term 
 
        | Ciprofloxacin HCl 
 CIs/Precautions
 |  | Definition 
 
        | 1.  hypersensitivity to quinolones 2.  children, adolescents or pregnant women due to permanent lesions in weight-bearing joints
 3.  Theophylline
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | N, rash, D, sun sensitivity, dizziness |  | 
        |  | 
        
        | Term 
 
        | Ciprofloxacin HCl 
 Pt consultation
 |  | Definition 
 
        | avoid sunlight 
 DC if rash develops
 
 drink 8 oz
 
 do not take antacids (Ca, Zn, or Fe).  take med 2 h before or 6 h after these products
 |  | 
        |  | 
        
        | Term 
 
        | Promethazine HCl 
 Brand Name
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Promethazine HCl  Dosage forms |  | Definition 
 
        | Tablets:  12.5, 25, and 50 mg Syrup plain:  6.25 mg/5 mL Suppositories:  12.5, 25, and 50 mg Injection:  25 mg/mL and 50 mg/mL |  | 
        |  | 
        
        | Term 
 
        | Promethazine HCl  FDA indications/Dosages |  | Definition 
 
        | 1.  Management of perennial & seasonal allergic rhinitis, vasomotor rhinitis, allergic conjunctivitis, uncomplciated allergic skin manifestation of urticaria & angioedema, amelioration of allergic rxns to blood or plasma, demographism & combo therapy in anaphylactic rxns 2. control of motion sickness 3.  control of N & V 4.  sedation |  | 
        |  | 
        
        | Term 
 
        | Promethazine HCl 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Promethazine HCl  Drug interactions |  | Definition 
 
        | 1.  AC may decrease effects 2.  OH and CNS depressants 3.  Metrizamide decrease seizure threshold 4.  Barbiturates decrease actions |  | 
        |  | 
        
        | Term 
 
        | Promethazine HCl CIs/Precautions |  | Definition 
 
        | 1.  Hypersensitivity to phenothiazines 2.  pts w/ lower respiratory tract sxs 3.  pediatric pts <2 y/o due to the potential for fatal respiratory depression 4.  injection in comatose states & pts who have taken lg amts of CNS depressants & should not be given by the SQ or intraarterial route |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Drowsiness, rash, N, V, blurred vision, dry mouth, & dizziness |  | 
        |  | 
        
        | Term 
 
        | Promethazine HCl 
 Pt consultation
 |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Tablets:  100 and 300 mg Solution for injection:  500 mg in a 30 mL single dose vial
 |  | 
        |  | 
        
        | Term 
 
        | Allopurinol 
 FDA indications/Dosages
 |  | Definition 
 
        | 1.  Gout & uric acid nephropathy w/ or w/o sxs of gout 2.  Prevention of UA nephropathy in pts undergoing vigorous therapy of neoplastic disease
 3.  Prevention of flare-up of acute gouty arthritis
 4.  Secondary hyperuricemia associated w/ malignancy
 5.  tx of recurrent ca oxalate stones
 |  | 
        |  | 
        
        | Term 
 
        | Allopurinol 
 Pharmacology/Pharmacokinetics
 |  | Definition 
 
        | competitively inhibits xanthine oxidase which is the enzyme responsible for the conversion of hypoxanthine to xanthine to UA |  | 
        |  | 
        
        | Term 
 
        | Allopurinol 
 Drug interactions
 |  | Definition 
 
        | 1.  Increase AMP-induced skin rash 2.  Increases teh pharmacological & toxic effects of orally thiopurines & chlorpropamide
 |  | 
        |  | 
        
        | Term 
 
        | Allopurinol 
 CIs/Precautions
 |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Drowsiness, D, N, V, abd pain, & RASH |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Compliance with therapy is essential.  May take one or more weeks to reach maximum effectiveness 
 High fluid intake during therapy is beneficial to help prevent kidney stone formation
 |  | 
        |  |