03/15 Revised BCPS PharmD, Traugott, Kristi PharmD; Li, Julius
Peptostreptococci
spp. Propionibacterium Staphylococci
Micrococci Enterococci
Diphtheroids Streptococci
Streptococci spp. Candida
Staphylococci spp. Lactobacillus
flora Skin spp. Clostridium
spp. Bacteroides
Enterobacteriaceae
flora Gut
Yeasts
daptomycin aminoglycosides, Ex: antibiotics lactam - beta Ex: spp. Moraxella
spp. Haemophilus ratio Cmax:MIC maximizing by T>MIC extending by efficacy increases infusion
spp. Neisseria Less frequent but higher doses increases efficacy efficacy increases doses higher but frequent Less - extended or administration frequent More
Diphtheroids
concentrations peak maximizing by killing Optimize MIC above time maximizing by killing Optimize
Staphylococci
Streptococci
dependent - Concentration dependent - Time
flora Respiratory
spp. Actinomyces
etronidazole M luoroquinolones F hloramphenicol C ulfonamides S
spp. Fusobacterium
arbapenems C enicillins P etracyclines T (lincosamides) lindamycin C
spp. Porphyromonas
ephalosporins C ancomycin V rimethoprim T (macrolides) rythromycin E
Diphtheroids
spp. Lactobacillus ” Murder Cell Complete For Proficient Very “ ” bacteriostatic for ECSTaTiC “
Staphylococci
Streptococci Bactericidal versus Bacteriostatic
flora Oral
live” normally bacteria “Where
Pharmacodynamics & Pharmacokinetics Antibiotic
Man Microbiome
Pharmacotherapy Antibiotic for Guide Pocket
Clarithryomycin
Aminoglycosies
Metronidazole Nitrofurantoin
Azithromycin
Ciprofloxacin
Moxifloxacin
Levofloxacin
Meropenem
Vancomycin Daptomycin
Clindamycin
Quinu/Dalfo
Doxycycline Minocycline
Ceftazidime Ceftriaxone
Cefuroxime
Polymyxins
Aztreonam
Ceftaroline Ertapenem
Tigecycline
Penicillin G Penicillin
Amox
Imipenem
Ampicillin TMP
Amp
Cefepime
Cefazolin
Cefoxitin
Linezolid
Pip
Drug Oxacillin
-
-
-
- Tazo
SMX
Sulb Bug Clav
Beta-hemolytic streptococci * + + + + + + + + + + + + + + + + + ± + + + + + + + ± + + Viridans group streptococci + + + + + + + + + + + + + + + + + + + + + + + + + + Streptococcus pneumoniae + + + + + + + + + + + + + + + + + + + + + + + + + + Staphylococcus aureus (MSSA) ± * + + + * + + + + + + + + + + + + + + + + + + + + + + Staphylococcus aureus (MRSA) + + + + + + * + + + + + + ± ± Enterococcus faecalis + * + + + + + + + + + + + + + + Enterococcus faecium ± + + + + + + + + + + Escherichia coli + + + + + + + + + + + + + + + + + + + + + + + + + Klebsiella spp. + + + + + + + + + + + + + + + + + + + + + + + + Enterobacter spp. + + + * + + + + + + + + + + + + + + + Citrobacter spp. + + + * + + + + + + + + + + + + + + + Serratia spp. + + + * + + + + + + + + + + + + + Proteus spp. + + + + + + + + + + + + + + + + + + + + Acinetobacter spp. + + + + + + + + + + + + + + + + Pseudomonas aeruginosa + + + + + + + + + + + Stenotrophomonas maltophilia ± + + + * Bacteroides spp. + + + + + + + + ± ± + + + + + + + Prevotella spp. + + + + + + + + + + + + + + + + +
Clostridium spp. + + + + + ± ± + ± ± ± ± + + + + ± ± + + + + + + + Refer to hospital to Refer antibiogram susceptibilityfor of specific rates organisms
Peptostreptococcus spp. + + + + + + + + + + + + + + + + + + + + + + + + ± Spectrum of Activity of Spectrum Against Common Bacteria Atypicals + + + + + + + +
* = drug of choice Julius Li, PharmD; Kristi Traugott, PharmD, BCPS Revised 03/15 Antibiotic Pharmacotherapy by Class Refer to Guidelines for Dosing in Renal Failure for both dosing in normal renal function and renal dose adjustments Antibiotic Adverse Reactions Drug Interactions Clinical Pearls
Penicillins Generally drugs of choice for bacteria once susceptibility known Penicillin G, oxacillin, None (e.g. MSSA, penicillin-susceptible S. pneumoniae, ampicillin- ampicillin, amoxicillin susceptible enterococci) Beta-lactam inhibitor Excellent anaerobic activity combinations Sulbactam has unique activity against Acinetobacter spp. (doses amoxicillin-clavulanate, None based on sulbactam, >6 g/day) ampicillin-sulbactam, Consider amox-clav 500-125 mg q8h dosing for gram-negative, an- piperacillin-tazobactam GI upset (nausea, diarrhea) aerobic, or mixed infections (more clavulanate needed) Hypersensitivity reactions Cephalosporins Leukopenia, thrombocytopenia (rare) Cross-reactivity with penicillin allergy <5% Cefazolin, ceftriaxone, Neurologic (altered mental status, seizures) None Caution with third generation cephalosporins (e.g. ceftriaxone) and ceftazidime, cefepime, Interstitial nephritis SPACE bugs+ (ampC producers) ceftaroline Hepatotoxicity (oxacillin) Carbapenems Generally reserved for multidrug resistant gram-negatives (MDR-GN) Ertapenem, imipenem, Drug of choice for ESBL producers None meropenem, doripenem Excellent anaerobic activity Cross-reactivity with penicillin allergy <5% Monobactams Generally reserved for severe penicillin allergy (e.g. anaphylaxis), but None Aztreonam may cross-react with ceftazidime allergy Fluoroquinolones GI upset (nausea, vomiting, diarrhea) Ciprofloxacin Neurologic (dizziness, AMS, seizures) Increasing resistance may limit use, particularly with E. coli Moxifloxacin Phototoxicity Caution with cations (reduced Higher dose for P. aeruginosa (e.g. cipro 750 mg q12h, levo 750 q24h) Levofloxacin Tendonitis, cartilage erosion bioavailability) Highly bioavailable, PO = IV QT prolongation Inhibits 1A2 (cipro) Moxifloxacin = poor urine penetration (not used for UTIs) Dysglycemia QT prolongation risk = moxi > levo >> cipro Peripheral neuropathies Tetracyclines GI upset (nausea, vomiting, epigastric distress) Highly bioavailable, PO = IV (doxy, mino) Doxycycline Photosensitivity Caution with cations (reduced Tige = severe nausea, may need scheduled antiemetics pre-dose Minocycline Teeth discoloration bioavailability) Mino, tige = has activity against multidrug resistant organisms (even Tigecycline Vertigo (minocycline) if tetra or doxy resistant)
Macrolides GI upset (nausea, vomiting, diarrhea) Erythromycin, azithromy- Inhibits 3A (ery > clari >> azi) QT prolongation risk = ery >> clari > azi QT prolongation cin, clarithromycin Glycopeptides Red man syndrome Red man syndrome can be prevented by slowing infusion rates or Vancomycin Nephrotoxicity None premedicate with diphenhydramine Neutropenia (rare) IV vanc for systemic infections, PO vanc for C. difficile infection Cyclic Lipopeptide Generally reserved for severe, resistant gram-positive infections (e.g. Skeletal muscle toxicity Daptomycin None MRSA, VRE) if vancomycin failure or resistant Eosinophilic pneumonia Not for pulmonary infections (deactivated by lung surfactant) Oxazolidinone Generally reserved for severe, resistant gram-positive infections (e.g. Linezolid MRSA, VRE) if vancomycin failure or resistant Thrombocytopenia Inhibits MAO (weak) Highly bioavailable, PO = IV Peripheral neuropathies p-glycoprotein substrate Higher toxicity risk with long-term therapy (>2 weeks) Higher risk for serotonin syndrome with due to MAO inhibition with serotonergic agents (e.g. SSRIs, TCAs) and foods (e.g. red wine) Lincosamide GI upset (diarrhea > nausea, vomiting) Increasing resistance in S. aureus and streptococci may limit use None Clindamycin Elevated LFTs (minor) Increasing resistance in anaerobes, particularly Bacteroides spp. Sulfonamides Hypersensitivity reactions Highly bioavailable, PO = IV Trimethoprim- Leukopenia, anemia None Dose for severe infections = 15 mg/kg/day based on TMP component sulfamethoxazole Hyperkalemia, renal failure (e.g. PCP, Nocardia spp.) Nitroimidazole Highly bioavailable, PO = IV GI upset (nausea) Metronidazole Excellent anaerobic activity Peripheral neuropathy None Avoid alcohol due to disulfiram reaction Taste disturbances (metallic) Higher risk for peripheral neuropathies with long-term therapy Nitrofurans Peripheral neuropathy Only used for UTIs, but without pyelonephritis Nitrofurantoin Pulmonary toxicity None Do not use with poor renal function (low urinary penetration) Hepatotoxicity (rare) Low resistance = good option for multidrug resistant organisms Aminoglycosides Nephrotoxicity Tobramycin preferred for P. aeruginosa infections Gentamicin, tobramycin, Ototoxicity None May be used synergistically for severe gram-positive infections amikacin Vestibular toxicity Ami = may have activity even if gent or tobra resistant Polymyxins Nephrotoxicity Last line for MDR-GNs due to high toxicity risk and limited efficacy None Colistin, polymyxin B Neurotoxicity (oral/peripheral paresthesias) Consider polymyxin B for systemic infections and colistin for UTIs Julius Li, PharmD; Kristi Traugott, PharmD, BCPS Revised 3/15 + SPACE bugs = Serratia marcescens, Pseudomonas aeruginosa, Acinetobacter baumannii, Citrobacter freundii, Enterobacter spp. Approfed by P&T Committee 6/2015