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195 Cards in this Set
- Front
- Back
Prevention of Type 2 Diabetes
|
Glucose intolerance precedes the development of diabetes
screening tests can identify persons at high risk |
|
Insulin
|
Typical production by non-diabetic adult is .2-.5 U/kg/day
Aprrox 50:50 split between basal and pranidal (in response to meals) 50% cleared through liver so [portal venous]> [systemic] |
|
Formulation of Insulin
|
Short Acting
Intermediate Acting (complexed with protamine) Long-acting (crystal suspensions with Zn) |
|
Site of Insulin Injection
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Abdomen> buttock> ant thigh> dorsal arm
|
|
Depth of Insulin Injection
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Intramuscular > subcutaneous
|
|
Absorption from these sites compared to IV administration
|
Gives systemic levels > portal vein
Slow in onset (30 - 120 min for peak levels) Slow in offset (up to 6hrs)- risk of post-prandial hypoglycemia |
|
Sulphonylureas (1st gen)
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Chlorpropamide
Tolbutamide (Obsolete) |
|
Sulphonylureas (2nd gen)
|
Glibenclamide
Gliclazide |
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Actions of Sulphonylureas
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Acutely release Insulin by depolarizing B-Islet cells
Effect not sustained chronically Significant extapancreatic effects (upregulation of Insulin receptors) |
|
How much more potent are second generation sulphonylureas than first generation?
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about 100x
|
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Side effects of Sulphonylureas
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Hypoglycemia
Hyponatraemiea (potentiate ADH action) |
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Biguandes (metformin) effect on insulin release?
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Do not cause hypoglycemia even in overdose
|
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Biguandes (metformin) action?
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appears to have post-receptor effect on insulin action
|
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Biguandes (metformin) used in conjuction with?
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Sulphonylureas
|
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Rare problem associated with Biguandes (metformin)
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Lactic Acidosis (<1 in 10000 patient-years)
|
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Biguandes (metformin) avoided if? (contraindications)
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Significant hepatic/renal impairment
|
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Thiazolidinediones (-glitazones) effect on insulin?
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dos not effect insulin function in normal tissues
effective in various insulin-resistant states |
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Do Thiazolidinedione (-glitazones) cause hypoglycemia? why or why not?
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do not cause hypoglycemia because it doesnt affect insulin function in normal tissues
|
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How do cyclooxygenase's (Cox Enzymes) work?
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Cyclooxygenase converts arachidonic acid (AA) into various prostaglandins (PGs)
|
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What forms of Cox Enzymes are there?
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Cox-1, Cox-2, Cox-3
|
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Cox-1 inhibited by?
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Asprin, advil, aleve, voltaren, daypro, and others
|
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Cox-2 inhibited by?
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cox-1 inhibitors, vioxx, and celebrex
|
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Cox-3 inhibited by?
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Cox-1, 2 inhibitors, and tylenol
|
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NSAID function and effects?
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block the activity of COX's
decrease pain, inflammation, and fever prevent clot formation (heart attack/stroke prevention) Possible prevention of cancer via COX-2 alteration |
|
Aspirin
|
Many Trade Names
Most widely used NSAID for analgesic and anti-inflammatory effects Used for antipyretic an danticoagulant effects |
|
Diclofenac
|
Voltaren
More potent that naproxen and several other NSAIDs |
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Diflunisal
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Dolobid
Has potency 3-4 times greater than aspirin For analgesic and anti-inflammatory, not for antipyretic activity |
|
Etodolac
|
Lodine
Analgesic/Anti-inflammatory fewer side effects than most NSAIDs may have gastric sparing properties |
|
Ibuprofin
|
Motrin, many others
first nonaspirin NSAID, fewer GI side effects |
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Ketoprofen
|
Orudis, Oruvail, others
similar to aspirin relatively short half life (1-2hrs) |
|
Ketorolac
|
Toradol
Administered orally or by intramuscular injection |
|
Nabumetone
|
Relafen
Analgesic/anti-inflammatory |
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Naproxen
|
Anaprox, Naprsyn, others
similar to ibuprofen |
|
Oxaprozin
|
Daypro
analgesic and anti inflammatory fewer side effects than other NSAIDs |
|
Piroxicam
|
Feldene
Long half-life (45 hrs) better tolerated than aspirin |
|
Asprin dosage
|
Analgesia- 325-650 mg every 4 hr
Anti-inflammation- 3.6-5.4 g/d in divided doses |
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Ibuprofen dosage
|
Analgesia- 200-400 mg every 4-6 hr as needed
anti-inflammation 600-800 mg q 4-6 h |
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Ketoprofen dosage
|
Analgesia- 25-50 mg every 4-6 hr
anti-inflammation- 150-300 mg/d in 3-4 divided doses |
|
Naproxen (Naprosyn) dosage
|
Analgesia- 500 mg initially, 250 mg every 6-8 hr
Anti-inflammation- 250, 375, 500 mg BID |
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Naproxen Sodium
|
Analgesia- 440-660 mg initially, 220 mg q 6-h hrs
Anti-inflammation- 440 mg BID |
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Complication of Chronic NSAID use
|
Liver and Kidney damage
Gastric Ulcers NSAID rebound effect |
|
Why does chronic NSAID use cause liver and kidney damage?
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inhibition of PGs that promote blood flow and function in liver and kidney
hepatic toxicity from chronic metabolism of NSAID |
|
Reyes syndrome
|
a condition that can be triggered when a child takes asprin after an acute viral or bacterial illness
high fever, encephalopathy, fatty liver |
|
who shouldn't take asprin?
|
children (and some teenagers) who have fevers
|
|
what should be taken instead of asprin in cases of reyes syndrome?
|
tylenol or ibuprofen
|
|
why shouldnt they take asprin in cases of reye's syndrome?
|
asprin irreversibly inhibits COX
Other NSAIDs and coxibs are reversible |
|
Other complications with NSAIDs
|
1% population is hypersentive to NSAIDS causing bronchospasm, rhinitis, urticaria, shock
NSAIDs may delay fracture healing by 1 or more weeks Should not be used in patients with acute bleeding/swelling (causes inhibition of COX-1, not allowing platelet aggregation and vasoconstriction) |
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Thromboxane function (TX's)
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blood clot remodeling in acute injuries
|
|
how are cox-1 and thromboxanes related?
|
inhibition of COX-1 may lead to increase edema in acute injuries
|
|
COX-2 Pharmaceutical Hypothesis
|
COX-2 specific inhibitors (coxibs) will reduce pain, fever, and inflammation without causing gastrointestinal or renal injury
|
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Acetaminophen (Paracetamol) function
|
Analgesic
Anti-pyretic not anti-inflammatory |
|
How does acetaminophen (paracetamol) work?
|
inhibits COX-3
nociception and pyresis in the brain |
|
Dosing for acetaminophen (paracetamol)
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regular- 325-1000 mg q 4-6 hrs
8 hr 625-1250 mg q 8 hours max daily dose- 4000 mg |
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Concern with taking acetaminophen (paracetamol)?
|
liver toxicity
|
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Corticosteroid
|
steroid hormones produced by adrenal cortex
|
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Glucocorticoids
|
Metabolism, anti infammation, immune modulation
|
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Beclomethasone
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Beclovent, vancerilill,, others
Topicak, inhalation, nasal |
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Cortisone
|
Cortone
systemic |
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Dexamethasone
|
Decadron, Dexasone, others
Systemic, Topical, ophthalmic, otic, nasal |
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Ruocinolone
|
Fluorsyn, Synatar, others
Topical |
|
Ruticason
|
Cultivate, Flonase
Topical, Nasal |
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Hydrocortisone
|
Cortef, Dermcort, hydrocortone, many others
sysetmic, topical, ophtlamic |
|
Methylprednisolone
|
Medrol, others
systemic |
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Prednisone
|
Delatsone, Meticorten, others
systemic |
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Triamcinolone
|
azmacort, artiscort, nasacort, others
systemic, topical inhalation nasal |
|
Osteoarthritis
|
Most common type of arthritis
Characterized by the progressive loss of joint cartilage and overgrowth of subchondral bone |
|
Hyaluronan
|
GAG that helps to hydrate and lubricate the joint
|
|
Glucosamine and Chondroitin
|
precursor molecules for many of the more complicated molecules that make up articular cartilage and synovial fluid
glucosamine- 1500 mg/day chondroitin- 1000 mg/day Methylsulfonylmethane (MSM)- 1000-4000 mg/day |
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Rheumatoid Arthritis
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Autoimmune disorder characterized by sever inflammation of they synovium
|
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What is RA caused by?
|
overproduction of inflammatory cytokine (TNF-alpha)
|
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DMARDs
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Disease-modifying antirheumatic drugs designed to reverse or halt the progression of RA
|
|
Gold Drugs for RA
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Auranofin (Ridaura)- Oral
Intramuscular- Aurothioglucose (Solganal) |
|
Leflunomide (Arava)
|
inhibits synthesis of RNA precursors in lymphocytes
effective in reducing pain and joint erosions |
|
Methotrexate (Rheumatrex)
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most effective DMARD
limits lymphocyte proliferation |
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TNF-alpha inhibitors
|
Entancercept (Enbrel)
Infliximab (Remicade) Adalimumab (Humira) |
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Alpha-1 Receptor acts on?
|
vascular smooth muscle: vasoconstriction
|
|
Agonist use alpha-1 receptor?
|
Hypotension, Nasal congestion, Paroxysmal supraventricular tachycardia
|
|
Antagonist use alpha-1 receptor?
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Hypertension
|
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Alpha-2 receptor acts on?
|
CNS synapses (inhibitory)
|
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Alpha-2 receptor Agonist Use
|
Hypertension
Spasticity |
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Alpha-2 receptor antagonist use
|
No significant clinical use
|
|
Beta-1 Receptor primary receptor location response when stimulated?
|
Heart: increased heart rate and force of contraction
|
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Agonist use Beta-1 receptor?
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cardiac decompensation
|
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Antagonist Use
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Hypertension
Arrhythmia Angina pectoris heart failure prevention of reinfarction |
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Beta-2 receptor primary receptor location response when stimulated
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bronchioles- bronchodilation
uterus- relaxation |
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Beta-2 receptor agonist use
|
prevent bronchospasm, premature labor
|
|
Beta-2 receptor antagonist use
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no significant clinical use
|
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alpha 1 adrenergic receptor activation causes
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smooth muscle contraction and vasoconstriction
|
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Acute hypotension characterized by?
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shock, general anesthesis
|
|
treatment of hypotension?
|
Mephenteraine (Wyamine) and Methoxamine (Vasoxyl)
|
|
Treatment for blood shot eyes
|
tetrahyrozoline (Visine)
|
|
Nasal congestion/bloody nose (epistaxis) treatment
|
phenylephrine (neo-synephrine)
oxymetazoline (afrin) pseudoephedrine (sudafed) |
|
Mixed alpha/beta agonists do what
|
activate both alpha and beta agonists
|
|
mixed alpha/beta agonists
|
Amphetamine, epinephrin, norepinephrine
|
|
alpha adrenergic receptor antagonists
|
primarily used to cause peripheral vasodilation
|
|
alpha adrenergic receptor antagonists
|
Prazosin (minipress)
Terazosin (Hytrin) Doxazosin (Cardura) |
|
Beta adrenergic receptor antagonists are used?
|
to decrease heart rate and cardiac contractility
|
|
Atenol
|
Trade Name- Tenormin
Selectivity- Beta-1 Primary Indications- Angina pectoris, hypertension, prevent reinfarction |
|
Carteolel
|
Cartrol
Nonselective Hypertension |
|
Propranolol
|
Inderal
Nonselective Angina pectoris, arrhythmias, hypertension, prevent reinfarction, prevent vascular headache |
|
Timolol
|
Blocadren
Nonselective Hypertension, prevent reinfarction, prevent vascular headache |
|
ACE inhibitors (angiotensin converting enzyme) do what?
|
block the conversion of angiotensin 1 to angiotensin II
use dto treat mild-moderate hpyertension |
|
ACE inhibitors
|
Captopril (Capoten)
Lisonopril (Prinivil) |
|
Angiotension II receptor inhibitors
|
Losartan (Cozaar)
Valsartan (Diovan) |
|
Clacium channel blockers used to?
|
block the entry of Ca2+ into vascular smooth muscle cells
|
|
effects of ca2+ blockers?
|
lead to vasodilation, decreased heart rate, and cardiac contractility
|
|
Ca2+ blockers
|
Verapamil (Calan)
Diltiazem (Cardizem) |
|
Minoxidil
|
(Lontiten, Rogain)
Not commonly used for hypertension, comonly used for allopecia |
|
Hydralizine
|
(Apresoline)
used to treat hypertensive emergencies and preeclampsia |
|
Diazoxide
|
(Hyperstat)
Used to treat hypertensive emergencies and preeclampsia |
|
Atorvastatin
|
(Lipitor)
decrease cholesterol |
|
Simvastatin
|
(Zocor)
decrease cholesterol |
|
Pravastatin
|
(Pravachol)
decrease cholesterol |
|
enoxeparin
|
(Lovenox)
low molecular weight heparins inhibit synthesis and function of clotting factors |
|
Warfarin
|
(Coumadin)
inhibit synthesis and function of clotting factors |
|
Aspirin use as anticoagulant
|
inhibit platelet aggregation and platelet-induced clotting
|
|
Clopidogret
|
(Plavix)
inhibit platelet aggregation and platelet-induced clotting |
|
Biofilms are?
|
(slime) collections of various microorganisms in a community
|
|
Biofilm matrix provides?
|
protection, anchoring and nutrition for residnet
|
|
Triclosan works by and is used for?
|
inhibits bacterial fatty acid synthesis
antiseptic |
|
is triclosan more effective than standard soap in destroying bacteria?
|
no, but may have residual, long term benefits
|
|
Ethanal or isopropyl alcohol (60-70%) is used as and is effective against?
|
hand sanitizer
fairly effective against bacteria |
|
Hydrogen peroxide works by?
|
forming hydroxyl radicals which are potent membrane disruptors
|
|
Povidone-iodine works by and is effective against?
|
(Betadine)
Iodinates fatty acids and is fairly effective against most microorganisms |
|
Chlorhexidine gluconate works by and is used for?
|
(hibiclens) disrupts bacterial membranes and is used as antiseptic scrub
|
|
B-lactam antibiotics
|
inhibit organziation of polysaccharide layers of cell wall
|
|
penicillins
|
first and most widely used antibiotics
penicillin (narrow) Amoxicillin (broad) Ampicillin (broad) |
|
cephalosporins
|
used for patients that have penicillin allergies or if penicillin is poorly tolerated or ineffective
|
|
Cephalexin
|
(Keflex) 1st generation cephalosporin for gram-broad and gram +cocci
|
|
Cefaclor
|
(Ceclor) 2nd generation cephalosprin
|
|
Ceftriaxone
|
(rocephin) 3rd generation (best of all cephalosporins)
|
|
Cefepime
|
(Maxipime) 4th generation
broad spectrum for both gram + and gram - |
|
Bacitracin
|
Topical formulation for broad spectrum
|
|
Vancomycin
|
antibiotic of last resort administered via PICC line
treatment of methicillin-resistant staphylococcus aureus |
|
Biofilms are?
|
(slime) collections of various microorganisms in a community
|
|
Biofilm matrix provides?
|
protection, anchoring and nutrition for residnet
|
|
Triclosan works by and is used for?
|
inhibits bacterial fatty acid synthesis
antiseptic |
|
is triclosan more effective than standard soap in destroying bacteria?
|
no, but may have residual, long term benefits
|
|
Ethanal or isopropyl alcohol (60-70%) is used as and is effective against?
|
hand sanitizer
fairly effective against bacteria |
|
Hydrogen peroxide works by?
|
forming hydroxyl radicals which are potent membrane disruptors
|
|
Povidone-iodine works by and is effective against?
|
(Betadine)
Iodinates fatty acids and is fairly effective against most microorganisms |
|
Chlorhexidine gluconate works by and is used for?
|
(hibiclens) disrupts bacterial membranes and is used as antiseptic scrub
|
|
B-lactam antibiotics
|
inhibit organziation of polysaccharide layers of cell wall
|
|
penicillins
|
first and most widely used antibiotics
penicillin (narrow) Amoxicillin (broad) Ampicillin (broad) |
|
Cephalosporins
|
used for patients that have penicillin allergies or if penicillin is poorly tolerated or ineffective
|
|
Generation 1 cephs
|
Cephalexin (Keflex)
|
|
Generation 2 cephs
|
Cefaclor (Ceclor)
|
|
Generation 3 cephs
|
Cetriaxone (Rocephin)
|
|
Generation 4 cephs
|
Cefepime (maximpime)
|
|
Bacitracin
|
Broad spectrum topical for both gram positive and negative
|
|
Vancomycin
|
antibioticof las resort for life threatening infections
|
|
Aminoglycosides
|
irreversibly bind to bacetrial ribosomes
Gentamycin, Kanamcin (kantrax) neomycin, streptomycin |
|
Macrolides
|
inhibit tRNA interaction with ribosomes
erythromycin, azithromycin (zithromax) |
|
Tetracyclines
|
inhibit translation or peptide bond formation in the ribosome
Doxycycline, Tetracycline |
|
Cephalosporins
|
used for patients that have penicillin allergies or if penicillin is poorly tolerated or ineffective
|
|
Generation 1 cephs
|
Cephalexin (Keflex)
|
|
Generation 2 cephs
|
Cefaclor (Ceclor)
|
|
Generation 3 cephs
|
Cetriaxone (Rocephin)
|
|
Generation 4 cephs
|
Cefepime (maximpime)
|
|
Bacitracin
|
Broad spectrum topical for both gram positive and negative
|
|
Vancomycin
|
antibioticof las resort for life threatening infections
|
|
Aminoglycosides
|
irreversibly bind to bacetrial ribosomes
Gentamycin, Kanamcin (kantrax) neomycin, streptomycin |
|
Macrolides
|
inhibit tRNA interaction with ribosomes
erythromycin, azithromycin (zithromax) |
|
Tetracyclines
|
inhibit translation or peptide bond formation in the ribosome
Doxycycline, Tetracycline |
|
Clindamycin
|
(Cleocin)
inhibit tRNA interaction with ribosomes |
|
Fluroquinolones
|
Ciprofloxacin (Cipro), Levofloxacin (Levaquin)
inhibt bacterial DNA/RNA synthesis or function |
|
Sulfonamides
|
Sulfadiazine (Silvadene)
|
|
Rifampin
|
(Rifadin)
|
|
Mupirocin
|
(Bactroban)
|
|
Imiquimod
|
(Aldara)
topical cream that promotes activation of immune system (HPV) |
|
Acyclovir
|
(Zovirax) topical or oral for herpes simplex
|
|
Valacyclover
|
(Valtrex)
pro form of acyclovier, oral can also be used for herpes zoster infection |
|
Docosanol
|
(Abreva)
topical for herpes labialis |
|
Ganciclover
|
(Cytovene)
viral DNA polymerase inhibitor |
|
Valgancyclovir
|
(Valcyte)
prodrug of ganciclovir |
|
Penciclovir
|
(Denavir)
herpes zoster and simplex, viral DNA polymerase inhibitor |
|
Famciclover
|
(Famvir)
prodrug of penciclovir |
|
Oseltamivir
|
(Tamiflu)
influencza A and B |
|
Zanamivir
|
(Relenza)
influenza a and b inhibit viral budding/shedding from host cells |
|
Amantadine
|
(Symmetrel)
influenza A inhibit the release of viral RNA from the capsid |
|
Rimantadine
|
(flumadine)
influenza A inhibit the release of viral RNA from the capsid |
|
Nucleoside revers transcriptase inhibitors
|
blocks viral (and non-viral) DNA synthesis
|
|
Azidothymidine (AZT)
|
Retrovir, Zidovudine
|
|
Non-nucleoside revers transcriptase inhibitors
|
efavirenz (sustiva)
|
|
Protease Inhibitors (PI)
|
Atanzavir (Reyataz)
|
|
HIV Integrase Inhibitors
|
Raltegravir (Isentress)
Block the HIV integrase enzyme |
|
HIV Entry inhibitors
|
Enfuvirtide (Fuzeon)
|
|
Permethrin
|
topical anti lice and scabies
|
|
Ivermectin
|
(stromectol)
oral anti lice and scabies |
|
Tolnaftate
|
(tinactin)
topical anti fungal |
|
Ketoconzazole
|
(Nizoral
topical anti fungal |
|
Miconazole
|
(monistat)
topical or oral anti fungal |
|
Lamisil
|
Terbinafine
topical or oral antifungal |
|
Praziquantel
|
(biltricide) increase Ca2+ permeatbility anti worm
|
|
Niclosamide
|
(Niclocide)
anti worm |