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Index

A

Abacavir (ABC), 249–250, 265

A. baumannii, 47, 52, 77

carbapenems and, 97

polymyxins and, 163

Abdominal infections

intra-, 78, 99, 103, 130

lincosamides and, 161

Abdominal surgery, 84

Abscesses, 30

Absorption, antibiotic pharmacokinetics, 26–28

defined, 26–28

examples of, 27, 28

Acetazolamide, 158

Acinetobacter, 12–14

Actinobacillus, 13

Actinomyces, 9, 140, 160

Acute interstitial nephritis (AIN), 57, 67, 236

Acyclovir, 27

described, 235–237

Adefovir, 285–286

Adipose tissue, drug distribution into, 31

Adjusted body weight, 31

ADME (absorption, distribution, and metabolism/excretion), 25

Advenovirus, 7

Adverse consequences of antibiotic use

allergy, 43–44

guidelines, 53–54

resistance, 45–46

superinfection, 44–45

toxicities, 44

Adverse effects

of aminoglycosides, 124–126

of aminopenicillins, 70

of anti-cytomegalovirus agents, 240

of antifungal antimetabolites, 199–201

of anti-herpes simplex virus agents, 236

of anti-MRSA cephalosporins, 93–94

of antipseudomonal penicillins, 74

of antistaphylococcal penicillins, 67–68

of antiviral interferons, 272

of atovaquone, 297

of benzimidazoles, 301

of carbapenems, 102–103

of cephalosporin/beta-lactamase inhibitor combinations, 98–99

of cyclic lipopeptides, 152–153

of direct-acting antihepatitis C agents, 277–278

of echinocandins, 226

of entry and fusion inhibitors, 269–270

of ethambutol (EMB), 187–188

of fidaxomicin, 169–170

of first-generation cephalosporins, 81–82

of fluconazole, 206

of fluoroquinolones, 118–120

of folate antagonists, 156–157

of fourth-generation cephalosporins, 91–92

of glycopeptides, 108–109

of hepatitis B nucleoside analogs, 286

of integrase inhibitors, 266

of isoniazid, 181–183

of itraconazole, 210

of ivermectin, 310

of ketolides, 132–133

of lincosamides, 160–161

of long-acting glycopeptides, 114–115

of macrolides, 132–133

of monobactams, 106

of natural penicillins, 64–65

of neuraminidase inhibitors, 244

of nitrofurans, 144–145

of nitroimidazoles, 140–141

of non-nucleoside reverse transcriptase inhibitors (NNRTIs), 254–255

of nucleoside reverse transcriptase inhibitors (NRTIs), 250–251

of oxazolidinones, 136–137

penicillin/beta-lactamase inhibitor combinations, 75–76, 97

of pentamidine, 305–306

of polyenes, 196

of polymyxins, 164–166

of protease inhibitors, 260–261

of pyrazinamide, 185–186

of quinolines, 294–295

of ribavirin, 282

of rifamycins, 178–179

of second-generation cephalosporins, 84

of streptogramins, 148–149

of tetracyclines, 128–129

of third-Generation Cephalosporins, 88–89

of varicella-zoster virus (VZV) agents, 236

of voriconazole, 214–215

Adverse reactions

of isavuconazole, 222

of posaconazole, 218

Aeromonas, 12

α-hemolysis, 9

AIN. See Acute interstitial nephritis (AIN)

Albendazole

described, 301–303

hepatotoxicity and, 302

Allergy, antibiotic, 43–44

Aluminum, 28, 121

Amikacin, 124

described, 123

Aminoglycosides, 41, 50, 71, 106

adverse effects, 124–126

agents, 123

amikacin, 123, 124

gentamicin, 123, 124

mechanism of action, 123

nephrotoxicity and, 124

neuromuscular blockade and, 124

ototoxicity and, 124

spectinomycin, 123

spectrum, 124

streptomycin, 123

tobramycin, 123, 124

Aminopenicillins, 27, 62, 69–71

adverse effects, 70

agents of, 69

amoxicillin, 69

ampicillin, 69

described, 69–71

diarrhea and, 70

enterococci and, 71

mechanism of action, 69

otitis media (ear infection) and, 71

spectrum, 69

streptococcal pharyngitis (strep throat) and, 70–71

Amodiaquine, 293–296

Amoxicillin, 27, 69, 70

Amoxicillin/clavulanate, 75–76

Amphotericin B

described, 195

lipid formulations of, 195

Ampicillin, 20

described, 69

susceptibility breakpoints, 38

Ampicillin/sulbactam, described, 75–76

Anaerobes

cephalosporins and, 84, 99

cephamycins and, 84

penicillins and, 75

Anaerobic intra-abdominal infections, 161

Anaphylaxis, 43, 57, 80, 103

Anidulafungin, described, 225–228

Antacids, 28

Antibiotic(s)

avoiding using to treat colonization or contamination, 53

bioavailability of, 26–28

clinically useful spectra of activity for empiric selection of, 318–320

defined, 15

guidance for utilizing, 53–54

macrolide, 29

susceptibility testing of, 35–39

using the proper dose, 54

using the shortest effective duration of therapy, 54

Antibiotic allergy, 43–44

Antibiotic pharmacodynamics

defined, 35

pharmacokinetic/pharmacodynamic relationships, 41–42

static versus cidal, 39–41

susceptibility testing, 35–39

Antibiotic pharmacokinetics

absorption, 26–28

defined, 25

distribution, 29–31

metabolism/excretion, 31–33

phases and parameters, 26

Antibiotic pressure, and collateral damage, 50–51

Antibiotic resistance, 45–46, 47–54

active efflux, 49, 50

antibiotic pressure and collateral damage, 50–51

avoiding using antibiotics to treat colonization or contamination, 53

causes of, 47

coming from, 48

decreased permeability, 48, 50

enzymatic modification, 49, 50

ESKAPE pathogens, 51–52

guidelines for utilizing antibiotics, 53–54

mechanisms of, 48–50

preventing, 52–53

target site changes, 49, 50

using narrow-spectrum agent, 53–54

using the proper dose, 54

using the shortest effective duration of therapy, 54

Antibiotic toxicities, 44

Anti-cytomegalovirus agents, 239–242

adverse effects, 240

cidofovir, 239–242

foscarnet, 239–242

ganciclovir, 239–242

mechanisms of action, 239

valganciclovir, 239–242

Antifungal antimetabolites

adverse effects, 199–201

agents, 199

flucytosine (5-FC), 199

mechanism of action, 199

Antifungals

clinically useful spectra of activity for empiric selection of, 321

introduction to, 191–193. See also individual drugs

Anti-herpes simplex virus, described, 235–237

Anti-herpes simplex virus agents, 235–237

acyclovir, 235–237

adverse effects, 236

famciclovir, 235–237

mechanism of action, 235

valacyclovir, 235–237

Anti-infective, defined, 15

Anti-infective drug, 15

Antimicrobial, defined, 15

Antimicrobial agents, 16, 17–18, 61

Antimicrobial chemotherapy, 16

Antimicrobial prophylaxis, 16–17

Antimicrobial resistance, 18

Anti-MRSA cephalosporins, 93–95

adverse effects, 94–95

agent, 93

ceftaroline, 93

mechanism of action, 93–94

spectrum, 94

Antimycobacterial drugs. See also individual drugs

introduction to, 173–175

Antiparasitic drugs. See also individual drugs

introduction to, 289–291

Antiparasitics, 290

Antipseudomonal penicillins, 62, 73–74

adverse effects, 74

agents, 73

described, 73–74

mechanism of action, 73

piperacillin, 73

spectrum, 73

ticarcillin, 73

Antiretroviral drugs. See also individual drugs

introduction to, 247–248

Antiretrovirals, 33, 247

Antistaphylococcal penicillins, 67–68

adverse effects of, 67–68

agents of, 67

cloxacillin, 67

described, 67–68

dicloxacillin, 67

mechanism of action, 67

methicillin, 67

MSSA and, 68

nafcillin, 67

oxacillin, 67

phlebitis and, 68

spectrum, 67

Antiviral drugs. See also individual drugs

introduction to, 231–233

Antiviral interferons

adverse effects, 272

agents, 271

interferon-α 2a, 271–273

interferon-α 2b, 271–273

mechanism of action, 271

pegylated interferon-α 2a, 271–273

pegylated interferon-α 2b, 271–273

Arachnid, 289

Archaea, 4

Arteminsins, 290

Ascaris, 5, 290

Aspergillus, 5, 192

Aspiration pneumonia, 78

Atazanavir (ATV), 28, 33

described, 259–263

Atovaquone, 290, 298

adverse effects, 297

described, 297–299

mechanism of action, 297

Atovaquone/proguanil, 290, 298

Atripla, 253, 256

Atypical bacteria, 4

Avoidance of antibiotic use, 28, 53

Azithromycin, 20

described, 131

Azoles. See also individual drugs

introduction to, 203

multiple topical formulations, 203

Aztreonam

described, 105, 106

penicillin allergy and, 106

B

Bacillus, 9

Bacteria, microbiology of, 3–14

Bactericidal drugs, bacteriostatic versus, 39–40

Bacteriostatic drugs versus bactericidal drugs, 39–40

macrolides, 133

Bacteroides, 12

Bacteroides fragilis, 85

Bartonella, 13

Benzimidazoles

adverse effects, 302

mechanism of action, 301

Beta-lactamases

cephalosporins and, 57, 61, 80

penicillins and, 62–63, 67, 73, 75–78

Beta-lactams. See also individual drugs

beta-lactamase inhibitor combinations, 75–78

introduction to, 57–59

MRSA (methicillin-resistant Staphylococcus aureus) and, 58–59

MSSA and, 68, 89

seizures and, 58

Staphylococci and, 68, 69

Bioavailability, of antibiotics, 26–28

Blastomyces, 5, 192

Blood, concentration of antibiotic in, 29, 32

Boceprevir, 275–279

Body weight

adjusted, 31

ideal, 31

total or actual, 31

Bone marrow suppression, 250

Burkholderia, 12, 14, 164

C

Calcium, 28, 120

Campylobacter, 13

Candida, 5, 21, 23, 45, 53, 192

antimetabolites and, 199, 201

C. albicans, 21, 205, 209, 213, 214, 215, 217, 226

candidiasis, 198, 200, 205, 207, 216–217, 221, 223, 227

candiduria, 201, 216

C. glabrata, 206, 209, 214, 217, 222, 226

C. krusei, 199, 206, 209, 213, 217, 226

C. lusitaniae, 196, 205, 209, 213, 217, 226

C. parapsilosis, 205, 209, 213, 217, 226

C. tropicalis, 205, 209, 213, 217, 226

echinocandins and, 195, 223, 228

fluconazole and, 201, 228

non-albicans species of, 205

polyenes and, 225, 227

Candida albicans, 21

Capsomeres, 232

Carbapenem-resistant Enterobacteriaceae, 52

Carbapenems, 41, 57, 61, 101–104

adverse effects, 102–103

agents, 101

doripenem, 101

ertapenem, 101

imipenem/cilastatin, 101

mechanism of action, 101

meropenem, 101

penicillin allergy and, 103

spectrum, 101–102

Cardiobacterium, 13

Caspofungin, 21

described, 223–227

CDC, 51, 52, 291, 296

Cefaclor, described, 83

Cefadroxil, 81

Cefamandole, 83

Cefazolin, 20

described, 81

Cefdinir, 87

Cefepime

described, 91

susceptibility breakpoints, 38

Cefixime, 87

Cefmetazole, 83

Cefonicid, 83

Cefotaxime, 87

Cefotetan, 83

Cefoxitin, 83

Cefpodoxime, 87

Cefprozil, 83

Ceftaroline, 93–95

Ceftazidime, 42

described, 87

Ceftibuten, 87

Ceftriaxone, 20, 21, 30

described, 87

Cefuroxime, 27, 80, 85, 318

described, 83

Centers for Disease Control and Prevention (CDC), 291, 296

Central nervous system (CNS), 25

Cephalexin, 81

Cephalosporin/beta-lactamase inhibitor combinations, 97–99

adverse effects, 98–99

agents, 97

ceftazidime/avibactam, 97–99

ceftolozane/tazobactam, 97

mechanism of action, 98

spectrum, 98

Cephalosporins, 41. See also individual drugs

Acinetobacter and, 97

activity by generation, 80

alcohol and, 84

anaerobes and, 84, 99

anaphylaxis and, 80

anti-MRSA, 93–95

Bacteroides and, 85

beta-lactamases and, 57, 61, 80

bleeding and, 84

central nervous system infections and, 82, 84, 88

Clostridium and, 88

endocarditis and, 82, 94

Enterococci and, 81, 83, 87, 91

fifth-generation, 95

first-generation, 27, 81–82

fourth-generation, 91–92

GNRs and, 97–98, 99

gonorrhea and, 85, 88, 89

Gram-positive organisms and, 81, 91, 92

Haemophilus and, 83

hives and, 80

introduction to, 79–80

Lyme disease and, 89

meningitis and, 92, 94

MRSA and, 93–95

MSSA and, 82, 89

Neisseria and, 83

neutropenia and, 89, 92

N-methylthiotetrazole (MTT), 84, 88

penicillin allergy and, 80

penicillinases, 80

phlebitis and, 82

pneumonia and, 85, 92, 94, 95

Pseudomonas and, 98–99

pyelonephritis and, 89

renal function/dysfunction and, 89, 92

respiratory tract infections and, 85, 89

second-generation, 83–85

skin infections and, 81, 82, 89, 94

Staphylococci and, 83

Streptococci and, 83, 87, 91, 94, 98

third-generation, 87–89

urinary tract infections and, 89

vitamin K and, 84, 88

Cephalothin, 81

Cerebrospinal fluid (CSF), 4

concentrations of antibiotics in, 29

Cestodes, 290

Chlamydia, 4

Chloroquine, 293, 295

described, 293–296

Cidofovir, 239–242

Cilastatin, 101

Cinchona tree, 293

Ciprofloxacin, 20, 21, 27

described, 117

fluoroquinolones and, 118

susceptibility E. coli to, 316

Citrobacter, 12

Clarithromycin, 33

described, 131

Clavulanate, 75–76

Clindamycin, 290

described, 159–160

Clindamycin/Primaquine, 290

Clinical and Laboratory Standards Institute (CLSI), 64

Clostridium, 9

Clostridium difficile, 23, 45, 52

Clostridium difficile-associated diarrhea, 45, 88

Cloxacillin, 67

CMV. See Cytomegalovirus (CMV)

CNS. See Central nervous system (CNS)

Cobicistat, 33

Coccidioides, 5, 192

Colistin (colistimethate sodium), 163

Collateral damage, antibiotic pressure and, 50–51

Colonization, avoiding using antibiotics to treat, 53

Combivir, 249

Community-acquired pneumonia, 20, 58, 78, 85, 94–95

Complera, 253

Contamination, avoiding using antibiotics to treat, 53

Corticosteroids, 303

Corynebacterium, 9

Cryptococcus, 5, 192

Cryptosporidium, 290

CSF. See Cerebrospinal fluid (CSF)

Cyclic lipopeptides

adverse effects, 152–153

agents, 151

daptomycin, 151

mechanism of action, 151

spectrum, 151

Cytomegalovirus (CMV), 4, 235, 239–242

D

Daclatasvir, 275–279

Dalbavancin, 113–115

Dalfopristin, 147

Dapsone, 155

Daptomycin, 41

described, 151

Darunavir (DRV), 28, 33

described, 259–263

Dasabuvir, 275–279

Definitive therapy, 18–19

examples of, 20–21

Descovy, 249

Diarrhea

aminopenicillins and, 70

Clostridium difficile-associated, 45, 88

macrolides and, 132, 133

penicillins and, 61–62

Dicloxacillin, 67

Didanosine, 251

described, 249–252

Dimorphic fungi, 5, 192

Direct-acting antihepatitis C agents, 275–279

adverse effects, 277–278

boceprevir, 275–279

grazoprevir, 275–279

mechanism of action, 276

paritaprevir, 275–279

protease inhibitors, 275–279

simeprevir, 275–279

telaprevir, 275–279

Distribution, antibiotic pharmacokinetics, 29–31

DNA

plasmids and, 48

synthesis, 155

topoisomerases, 118

Dolutegravir (DTG), 265–267

Doripenem

described, 101

Dosing issues

fluconazole, 206–207

glycopeptides and, 109–110

isavuconazole, 222–223

polyenes, 196–197

posaconazole, 218

voriconazole, 215

Doxycycline, 27, 290

described, 127

Drug-resistant Neisseria gonorrhoeae, 52

Drugs

absorption impaired by, 28

antibacterial, 15, 45

antifungal, 191–193

antimicrobial, 15

antimycobacterial, 173–175

antiparasitic drugs, 15, 289–291

antiretroviral, 33, 247–248

antiviral, 231–233

bacteriostatic. See Bacteriostatic drugs

with high bioavailability, 26–28

interactions, 32–33

with low bioavailability, 26–28

protein-bound, 30

E

EBV. See Epstein-Barr virus (EBV)

Echinocandins

adverse effects, 226

agents, 225

anidulafungin, 225, 226

caspofungin, 225, 226

mechanism of action, 225

micafungin, 225

Echinococcus, 290

E. coli, 4, 13

ampicillin and, 70

antibiotic susceptibility breakpoints, 38

nitrofurans and, 143

penicillins and, 70

susceptibility to ciprofloxacin, 316

Ectoparasites, 290

Efavirenz (EFV), 33

described, 253–257

Eikenella, 13

Elbasvir, 275–279

Elvitegravir (EVG), 33, 265–267

EMB. See Ethambutol (EMB)

Empiric regimens for common infections, 323–328

Empiric therapy, 17–18

examples of, 20

Emtricitabine (FTC), 265–267

described, 249–252

Endocarditis, 40

penicillins and, 65

Enfuvirtide (T20), 269–270

Entamoeba, 140, 290

Entecavir, 285–286

Enteric gram-negative rods, 13. See also Lactose-fermenting Gramnegative rods

Enterobacter, 12, 13

Enterobacter species, 52, 325

Enterococcus

cephalosporins and, 81, 83, 87, 91

glycopeptides and, 107

penicillins and, 70

Enterococcus faecalis, 9, 20

Enterococcus faecium, 9, 52, 107

Entry and fusion inhibitors

adverse effects, 269–270

dermatologic effects, 269

described, 269–270

hepatotoxicity and, 268–269

mechanism of action, 269

Epstein-Barr virus (EBV), 4

Epzicom, 249

Ertapenem, 22

described, 101

Erythromycin, 33, 131

Escherichia, 12

Escherichia coli. See E. coli

ESKAPE pathogens, 51–52

Ethambutol (EMB)

adverse effects, 187–188

described, 187–188

mechanism of action, 187

Mycobacterium avium-intracellulare complex, 187

Mycobacterium kansasii and, 187

Mycobacterium tuberculosis and, 187

Etravirine (ETR), 33

described, 253–257

Eukaryotes, 3, 5

Evotaz, 259

Excretion, antibiotic pharmacokinetics, 31–33

F

Famciclovir, 235–237

Fastidious organisms, 13, 14

Fidaxomicin

adverse effects, 169–170

agents, 169

mechanism of action, 169

spectrum, 169

Fifth-generation cephalosporins, 95

First-generation cephalosporins, 27, 81–82

adverse effects, 81–82

agents, 81

cefadroxil, 81

cefazolin, 81

cephalexin, 81

cephalothin, 81

mechanism of action, 81

spectrum, 81

Fluconazole, 21, 23, 27, 33, 203

adverse effects, 206

dosing issues, 206–207

introduction of, 205

mechanism of action, 205

Flucytosine (5-FC)

described, 199

HIV and, 200

Fluoroquinolones, 28, 41, 117–121

adverse effects, 118–120

agents, 117

ciprofloxacin, 117, 118

gemifloxacin, 117, 118

indications for, 121

levofloxacin, 117, 118

mechanism of action, 118

moxifloxacin, 117, 118

spectrum, 118

Folate antagonists

adverse effects, 156–157

agents, 155

dapsone, 155

mechanism of action, 155

pyrimethamine, 155

spectrum, 155–156

sulfadiazine, 155

sulfadoxine, 155

trimethoprim/sulfamethoxazole (TMP/SMX), 155

Fosamprenavir (FPV), 259–263

Foscarnet, 239–242

Fosfomycin, 143–145

Fourth-generation cephalosporins, 91–92

adverse effects, 91–92

agent, 91

cefepime, 91

mechanism of action, 91

spectrum, 91

Fulminant hepatic failure, 254–255

Fungus, 5, 290

Fusarium, 192

Fusobacterium, 12

G

Ganciclovir, 239–242

Gardnerella, 9

Gastrointestinal (GI) tract, tetracyclines and, 128

Gemifloxacin

described, 117

fluoroquinolones and, 118

Gentamicin, 124

described, 123

Genvoya, 265–267

Giardia, 5, 140, 290

Glucose fermenters, 12

Glucose/lactose fermentation, 13–14

Glycopeptides

adverse effects, 108–109

agents, 107

aminoglycosides and, 123

described, 107–111

dosing issues, 109–110

long-acting, 113–115

mechanism of action, 107–108

spectrum, 108

telavancin, 107

vancomycin, 107

Glycylcyclines, 127–130

GNRs. See Gram-negative rods (GNRs)

Gram-negative organisms, 4

cell walls of, 7

fastidious organisms, 14

glucose/lactose fermentation, 13–14

glycopeptides and, 108

Gram’s stain, described, 5–6

morphology, 12–13

peptidoglycan, 11

Gram-negative pathogens, 12

Gram-negative rods (GNRs)

cephalosporins and, 97–98, 99

penicillins and, 70–71, 73

third-generation cephalosporins and, 88

Gram-positive bacilli, 9

Gram-positive organisms, 4, 8

biochemistry and appearance on agar, 10

cell walls of, 6, 7

cephalosporins and, 81, 91, 92

colony clustering, 10

glycopeptides and, 108

Gram’s stain, described, 5–6

outermost membrane in, 6

penicillins and, 69, 74

rapid identification based on morphology, 8–9

Gram’s stain, 5–6

Gram staining, 17

Grazoprevir, 275–279

H

HACEK organisms, 13

Haemophilus, 13

cephalosporins and, 83

penicillins and, 69, 73

Haemophilus influenzae, 83

Helicobacter, 13

macrolides and, 132

Helminthes (worms), 301

Helminths, 5, 290

Hemoglobin, 283

Hepatic steatosis, 251

Hepatitis

pyrazinamide, 185, 186

pyrazinamide and, 185, 186

Hepatitis B nucleoside analogs, 285–286

adefovir, 285–286

adverse effects, 286

entecavir, 285–286

mechanism of action, 285

telbivudine, 285–286

Hepatitis C virus (HCV), 260, 272

Hepatotoxicity

entry and fusion inhibitors and, 269–270

nevirapine-induced, 254

non-nucleoside reverse transcriptase inhibitors (NNRTIs) and, 254

protease inhibitors and, 261

Herpes simplex, 6

Herpes simplex virus (HSV), 4

Herpes simplex virus (HSV), 235–237

Highly active antiretroviral therapy (HAART), 259

Histamine-2 receptor antagonists, 28

Histoplasma, 192

HIV

anti-herpes simplex virus agents and, 236

entry and fusion inhibitors and, 269, 270

flucytosine and, 200

hepatitis B nucleoside analogs and, 285–286

HSV outbreaks among, 236

non-nucleoside reverse transcriptase inhibitors (NNRTIs) and, 249,

250

nucleoside reverse transcriptase inhibitors (NRTIs) and, 249, 250,

252, 256

protease inhibitors and, 259, 260

susceptibility testing and, 233

thrombotic thrombocytopenic and, 236

valacyclovir and, 236

Hospital-acquired pneumonia, 20–21, 94

HSV. See Herpes simplex virus (HSV)

Human flora, 313

Hydroxychloroquine, 293–296

Hyperlipidemia, 251

Hypersensitivity

non-nucleoside reverse transcriptase inhibitors (NNRTIs) and,

254–255

NRTIs and, 250

I

Ideal body weight, 31

Imipenem, described, 101

Imipenem/cilastatin, 21

Immunosuppressive therapy, 16

Indinavir (IDV), 259–263

Infections

empiric regimens for common, 323–328

in neutropenic patients, 40

Infectious diseases, 19

case study, 21–22

definitive therapy, 18–19, 20–21

empiric therapy, 17–18, 20

prophylactic therapy, 16–17, 20

rapid diagnostics, 22–23

Injection site reactions, 269

Insulin resistance, 251

Integrase inhibitors, 265–267

adverse effects, 266

mechanism of action, 265

musculoskeletal effects, 266

renal effects, 266

Interferon-α 2a, 271–273

Interferon-α 2b, 271–273

Iron, 28

Isavuconazole, 203, 217

adverse reactions, 222

dosing issues, 222–223

mechanism of action, 221

Isoniazid, 28, 179

adverse effects, 181–183

described, 181–183

mechanism of action, 181

Isonizid, 188

Itraconazole, 28, 33, 203

adverse effects, 210

mechanism of action, 209

Itraconazole capsules, 28

Itraconazole solution, 28

Ivermectin, 290

adverse effects, 310

described, 309–311

mechanism of action, 309

K

Kaletra, 259

Ketoconazole, 203

Ketolides

adverse effects, 132–133

agents, 131

azithromycin, 131

clarithromycin, 131

described, 131–134

erythromycin, 131

mechanism of action, 131

spectrum, 132

telithromycin, 131

Kingella, 13

Klebsiella, 12, 13

Klebsiella pneumoniae, 21, 52

L

Lactic acidosis, 251

Lactobacillus, 9

Lactose-fermenting Gram-negative rods, 14. See also Enteric Gram-

negative rods

Lamivudine (3TC), 249–252

Ledipasvir, 275–279

Levofloxacin, 20, 27

described, 117

fluoroquinolones and, 118

susceptibility breakpoints, 37, 38

Lincosamides

abdominal infections and, 161

adverse effects, 160–161

agents, 159

clindamycin, 159–160

mechanism of action, 159

spectrum, 160

Linezolid, 27, 41

described, 135

Lipid formulations of amphotericin B, 195

Lipoatrophy, 251

Lipoglycopeptides, 107–111

Lipohypertrophy, 255

Lipopolysaccharide, 6

Listeria, 9

Long-acting glycopeptides, 113–115

adverse effects, 114–115

agents, 113

dalbavancin, 113

mechanism of action, 113–114

oritavancin, 113

spectrum, 114

Loracarbef, 83

M

Macrolides, 29, 33, 41

adverse effects, 132–133

agents, 131

azithromycin, 131

clarithromycin, 131

described, 131–134

erythromycin, 131

mechanism of action, 131

spectrum, 132

telithromycin, 131

Malaria, tetracyclines and, 126, 130

Malarone, 297

Mammals, 5

Maraviroc (MVC), 33, 269–270

MBC. See Minimum bactericidal concentration (MBC)

Mebendazole, 301–303

Mechanism of action

aminoglycosides, 123

aminopenicillins, 69

of antibiotic resistance, 48–50

anti-cytomegalovirus agents, 239

antifungal antimetabolites, 199

anti-herpes simplex virus agents, 235

anti-MRSA cephalosporins, 93–94

antipseudomonal penicillins, 73

antistaphylococcal penicillins, 67

antiviral interferons, 271

atovaquone, 297

benzimidazoles, 301

carbapenems, 101

cephalosporin/beta-lactamase inhibitor combinations, 98

cyclic lipopeptides, 151

direct-acting antihepatitis C agents, 276

echinocandins, 225

entry and fusion inhibitors, 269

ethambutol (EMB), 187

fidaxomicin, 169

first-generation cephalosporins, 81

fluconazole, 205

fluoroquinolones, 118

folate antagonists, 155

fourth-generation cephalosporins, 91

glycopeptides, 107–108

hepatitis B nucleoside analogs, 285

integrase inhibitors, 265

isavuconazole, 221

isoniazid, 181

itraconazole, 209

ivermectin, 309

ketolides, 131

lincosamides, 159

long-acting glycopeptides, 113–114

macrolides, 131

Monobactams, 105

natural penicillins, 63

neuraminidase inhibitors, 243

nitrofurans, 143–144

nitroimidazoles, 139

non-nucleoside reverse transcriptase inhibitors (NNRTIs), 253

nucleoside reverse transcriptase inhibitors (NRTIs), 249

oxazolidinones, 135

penicillin/beta-lactamase inhibitor combinations, 76

pentamidine, 305

polyenes, 195

polymyxins, 163

posaconazole, 217

protease inhibitors, 260

pyrazinamide, 185

quinolines, 293–294

ribavirin, 281

rifamycins, 177

second-generation cephalosporins, 83

streptogramins, 147

tetracyclines, 127

third-Generation Cephalosporins, 87

varicella-zoster virus (VZV) agents, 235

voriconazole, 213

Mefloquine, 296

described, 293–296

Meningitis, 40

cephalosporins and, 92, 94

Meropenem, 20

described, 101

Metabolism, antibiotic pharmacokinetics, 31–33

Metabolism/excretion

defined, 31–33

examples of antibiotics, 33

Methicillin. See also MRSA (methicillin-resistant Staphylococcus aureus); MSSA (methicillin-sensitive Staphylococcus aureus)

described, 67

Methicillin-resistant Staphylococcus aureus (MRSA), 21, 23

Metronidazole, 27, 33, 41, 139

MIC. See Minimum inhibitory concentration (MIC)

Micafungin, 225–228

Microbiological susceptibility testing

Microbiology of bacteria, 3–14

Microorganisms, relative sizes of, 6

Minimum bactericidal concentration (MBC), 40

Minimum inhibitory concentration (MIC), 35

breakpoint, 36

Minocycline, 127

Molds, 192

Monobactams, 41, 105–106

adverse effects, 106

agent, 105

aztreonam, 105

mechanism of action, 105

spectrum, 105

Moraxella, 13

Moulds, 5

Moxifloxacin

described, 117

fluoroquinolones and, 118

MRSA (methicillin-resistant Staphylococcus aureus)

beta-lactams and, 58–59

cephalosporins and, 93–94, 93–95

glycopeptides and, 107, 108, 110, 113

tetracyclines and, 128

MSSA (methicillin-sensitive Staphylococcus aureus)

beta-lactams and, 68, 89

ceftriaxone and, 89

cephalosporins and, 82, 89

glycopeptides and, 108, 110

penicillins and, 62, 68

M. tuberculosis

pyrazinamide and, 185

Mucorales, 192

Mycobacterium avium intracellularae (MAI or MAC), 20

Mycoplasma, 4

N

Nafcillin, 67

Natural penicillins, 63–65

adverse effects, 64–65

agents of, 63

endocarditis and, 65

mechanism of action, 63

narrow-spectrum beta-lactams and, 65

neurosyphilis and, 65

penicillin G, 63

penicillin V, 63

pharyngitis and, 65

spectrum, 64

susceptible streptococcal infections and, 65

syphilis and, 65

Neisseria, 13

Neisseria gonorrheae, 83

Neisseria gonorrhoeae, 52

Neisseria meningitidis, 13

Nelfinavir (NFV), 259–263

Nematodes, 290

Nephrotoxicity

aminoglycosides and, 124

glycopeptides and, 108–109

NRTIs and, 251

pentamidine and, 306

protease inhibitors and, 261

Neuraminidase inhibitors, 243–245

adverse effects, 244

mechanism of action, 243

oseltamivir, 243–245

peramivir, 243–245

zanamivir, 243–245

Neuromuscular blockade, aminoglycosides and, 124

Neuropathy, NRTIs and, 250

Neutropenia, cephalosporins and, 89, 92

Neutropenic patients, infections in, 40

Nevirapine (NVP), 33

described, 253–257

Nevirapine-induced hepatotoxicity, 254

Nitrofurans

adverse effects, 144–145

agents, 143

described, 143–145

fosfomycin, 143

mechanism of action, 143–144

nitrofurantoin, 143

spectrum, 144

Nitrofurantoin, 32

bladder infections and, 32

described, 143

Nitroimidazoles

adverse effects, 140–141

agents, 139

mechanism of action, 139

metronidazole, 139, 140

spectrum, 140

tinidazole, 139

N-methylthiotetrazole (MTT) cephalosporins, 84

Nonfermenting Gram-negative rods, 14

Nonhemolytic, 9

Non-nucleoside polymerase inhibitors, 275–279

Non-nucleoside reverse transcriptase inhibitors (NNRTIs), 253–257

adverse effects, 254–255

CNS effects, 254

dermatologic effects, 254

hepatotoxicity and, 254

hypersensitivity and, 254–255

mechanism of action, 253

metabolic effect, 255

pregnancy/lactation and, 255

Nonsterile sites, infection in, 4

Nosocomial pneumonia, 77–78, 92, 104

NRTIs. See Nucleoside reverse transcriptase inhibitors (NRTIs)

NS5A inhibitors, 275–279

NS5B (polymerase) inhibitors, 275–279

Nucleic acid, 232

Nucleoside, 249–252

Nucleoside reverse transcriptase inhibitors (NRTIs)

adverse effects, 250–251

described, 249–252

extremities, 250

gastrointestinal effect, 250

hematological effect, 250

hypersensitivity and, 250

mechanism of action, 249

metabolic effect, 251

renal effect, 251

O

Obesity, 31

Ombitasvir, 275–279

Onchocerca, 311

Oral antibiotics, 27

Oral formulation

of colistin, 166

of isavuconazole, 222

of itraconazole, 210

of linezolid, 136–137

Oritavancin, 113

Oseltamivir, 243–245

Osteomyelitis, 40

Ototoxicity, aminoglycosides and, 124

Oxacillin, 67

Oxazolidinones

adverse effects, 136–137

agents, 135

linezolid, 135

mechanism of action, 135

spectrum, 135

tedizolid, 135

P

P450 substrates, 262

Paracoccidioides, 192

Parasites, 5

Parasitic mitochondria, 297

Paritaprevir, 275–279

Pasteur, Louis, 232

PEG. See Polyethylene glycol (PEG)

Pegylated interferon-α 2a, 271–273

Pegylated interferon-α 2b, 271–273

Pegylated interferons, 272

Penicillin(s), 31–32, 41. See also individual drugs

aerobes and, 75, 78

allergy and cephalosporins, 80

amino, 69–71

amoxicillin, 69–71

ampicillin, 69–71

anaerobes and, 75, 78

antibacterial activity of, 61–78

antipseudomonal, 73–74

antistaphylococcal, 67–68

beta-lactamases and, 62–63, 67, 73, 75–78

cloxacillin, 67–68

diabetic ulcers and, 78

diarrhea and, 61–62

dicloxacillin, 67–68

drug development, 62

E. coli and, 70

endocarditis and, 65, 68, 71

Enterococci and, 70, 71, 73, 74

GNRs and, 70–71, 73

Gram-positive organisms and, 74

Haemophilus and, 69, 73

introduction to, 61–62

IV therapy, 70

methicillin, 67–68

MSSA and, 62, 68

nafcillin, 67–68

natural, 63–65

otitis media and, 71

oxacillin, 67–68

penicillin G, 63–65

penicillin V, 63–65

pharyngitis and, 65, 71

phlebitis and, 68

piperacillin, 73–74

pneumonia and, 77–78

Pseudomonas and, 69, 76

renal function/dysfunction and, 61, 68

respiratory tract infections and, 78

skin infections and, 68

Staphylococci and, 67, 68–69

Streptococci and, 70, 73

syphilis and, 65

ticarcillin, 73–74

Treponema and, 64

UTIs and, 70

Penicillinases, 80

Penicillin/beta-lactamase inhibitor combinations, 75–78

adverse effects, 76–77

agents, 75–76

amoxicillin/clavulanate, 75–76

ampicillin/sulbactam, 75–76

mechanism of action, 76

piperacillin/tazobactam, 75–76

spectrum, 76

Penicillin G, 63–65

Penicillin V, 63–65

Pentamidine, 290

adverse effects (IV pentamidine), 305–306

cardiovascular effects, 305–306

described, 305–307

mechanism of action, 305

metabolic effects, 306

nephrotoxicity and, 306

renal effects, 306

respiratory effects, 306

Peptidoglycan, 6, 11

Peptococcus, 8, 313

Peptostreptococcus, 8

Peramivir, 243–245

Peripheral neuropathy, 250

Pharmacokinetic/pharmacodynamic (PK/PD) parameters, 41

Pharmacokinetics, phases and parameters, 26

Phlebitis

antistaphylococcal penicillins and, 68

cephalosporins and, 82

Piperacillin, 20

described, 73

Piperacillin/tazobactam, described, 75–76

Plasmodium (malaria), 5, 290

Pneumocystis, 290

Pneumocystis jirovecii, 289

Pneumocystis jirovecii (carinii) pneumonia, 20, 161

Pneumocystis pneumonia, 298, 305–307

Pneumonia

aspiration, 78

cephalosporins and, 85, 92, 94, 95

community-acquired, 20, 58, 78, 85, 94–95

glycopeptides and, 110–111

hospital-acquired, 20–21, 94

nosocomial, 77–78, 92, 104

penicillins and, 77–78

P. jirovecii, 161

Pneumocystis jirovecii (carinii), 20

tetracyclines and, 129

Polyenes

adverse effects, 196

agents, 195

amphotericin B, 195

dosing issues, 196–197

mechanism of action, 195

nystatin (topical), 195

Polyethylene glycol (PEG), 271

Polymerase chain reactions (PCR), 23

Polymyxin B, 163

Polymyxins

A. baumannii and, 163

adverse effects, 164–166

agents, 163

colistin (colistimethate sodium), 163

mechanism of action, 163

polymyxin B, 163

spectrum, 164

Posaconazole, 33, 203

adverse reactions, 218

dosing issues, 218

mechanism of action, 217

Posaconazole suspension, 28

P. ovale, 296

Prevention, of antibiotic resistance, 52–53

Prevotella, 12

Prezcobix, 259

Primaquine, 290, 296

described, 293–296

Prokaryotes, 3, 4, 231

Prophylactic therapy, 16–17

Prophylaxis/prophylactic therapy, 16–17

defined, 16–17

examples of, 20

Propionibacterium, 9, 140, 313

Protease inhibitors (PIs), 259–263

adverse effects, 260–261

cardiovascular effects, 260–261

gastrointestinal effects, 261

hepatotoxicity and, 261

mechanism of action, 260

metabolic effects, 261

nephrotoxicity and, 261

Proteus, 12, 118, 128

glycylcyclines and, 22

nitrofurans and, 144

Proton pump inhibitors, 28

Protozoa, 5, 290

Pseudomonas, 12, 14

cephalosporins and, 98–99

penicillins and, 69, 76

Pseudomonas aeruginosa, 52

Pulmonary aspergillosis, 20

P. vivax, 296

Pyelonephritis, 20

nitrofurans and, 143, 145

Pyrazinamide, 28, 183, 188

adverse effects, 185–186

described

hepatitis, 185, 186

mechanism of action, 185

M. tuberculosis and, 185

Pyrimethamine, 155

Pyrimethamine/Sulfadiazine, 290

Q

Quinidine, 293–296

Quinine, 293–296

Quinine/quinidine, 296

Quinolines, 290

adverse effects, 294–295

cardiovascular effects, 294

hematologic effects, 294

mechanism of action, 293–294

metabolic effects, 294

psychiatric effects, 294–295

systemic effects, 295

Quinupristin, 147

R

Rabies, 6

Raltegravir (RAL), 265–266

Renal function/dysfunction. See also Nephrotoxicity

cephalosporins and, 89, 92

nitrofurans and, 144, 145

penicillins and, 61, 68

Resistance, antibiotic, 45–46

Ribavirin

adverse effects, 282

described, 281–283

mechanism of action, 281

Rickettsia, 6

Rifabutin, 33

described, 177

Rifampin (rifampicin), 28, 33, 188

described, 177

Rifamycins

adverse effects, 178–179

agents, 177

mechanism of action, 177

rifabutin, 177

rifampin (rifampicin), 177

rifapentine, 177

rifaximin, 177

spectrum, 178

Rifapentine, 177

Rifaximin, 177

Rilpivirine (RPV), 28, 33, 253–257

Ritonavir, 33

Ritonavir (boosting dose: /r), 259–263

Ritonavir (full dose: RTV), 259–263

S

Salmonella, 12

Saquinavir (SQV), 259–263

Sarcoptes scabei, 289

S. aureus, 5

Scabies, 290

Scedosporium, 192

Schistosoma, 290

Second-generation cephalosporins, 83–85

adverse effects, 84

agents, 83

cefaclor, 83

cefamandole, 83

cefmetazole, 83

cefonicid, 83

cefotetan, 83

cefoxitin, 83

cefprozil, 83

cefuroxime, 83

loracarbef, 83

mechanism of action, 83

spectrum, 83

Seizures, beta-lactams and, 58

S. epidermidis, 10

Serratia, 12, 13

Shigella, 12

Short-acting lipoglycopeptides, 107–111

Simeprevir

described, 275–279

hepatotoxicity and, 277

Skin/soft tissue infections

cephalosporins and, 81, 82, 89, 94

Sofosbuvir, 275–279

Spectinomycin

described, 123

Spectrum of activity, 315–317

S. pneumoniae, 5

Staphylococci

beta-lactams and, 67, 68–69

Staphylococcus. See also MRSA (methicillin-resistant Staphylococcus aureus); MSSA (methicillin-sensitive Staphylococcus aureus)

beta-lactams and, 68, 69

cephalosporins and, 83

glycopeptides and, 113

penicillins and, 63, 67

Staphylococcus aureus, 4, 8, 21, 50, 52

Staphylococcus epidermidis, 8

Staphylococcus saprophyticus, 8

Stavudine (d4T)

described, 249–252

Stenotrophomonas, 12, 14

Sterile site, infection in, 4

Streptococcus, 6

antibiotic susceptibility break points, 38

penicillins and, 64

Streptococcus agalactiae (Grp B), 9

Streptococcus pneumoniae, 4, 9

Streptococcus pyogenes (Grp A), 9

Streptogramins

adverse effects, 148–149

agents, 147

mechanism of action, 147

quinupristin/dalfopristin, 147

spectrum, 148

Streptomycin, 123

Stribild, 265–267

Strongyloides, 290, 311

Strongyloides hyperinfection syndrome, 309

Sulfadiazine, 155

Sulfadoxine, 155

Sulfamethoxazole (SMX). See Trimethoprim/sulfamethoxazole

(TMP/SMX)

Superinfection, antibiotic, 44–45

Susceptibility testing of antibiotics, 35–39

T

Taenia, 5, 290

Tazobactam, 20. See also Piperacillin/tazobactam

Tedizolid, 135

Telaprevir, 275–279

Telavancin, 107

Telbivudine, 285–286

Telithromycin, 33, 131

Tenofovir (TDF), 265–267

Tenofovir alafenamide (TAF), 249–252

Tenofovir disoproxil fumarate (TDF), 249–252

Tetracycline(s), 28, 41

adverse effects, 128–129

agents, 127

described, 127–129, 127–130

doxycycline, 127

gastrointestinal (GI) tract and, 128

malaria and, 126, 130

mechanism of action, 127

minocycline, 127

MRSA and, 128

pneumonia and, 129

spectrum, 127–128

tetracycline, 127

tigecycline, 127

Thiabendazole, 301–303

Third-generation cephalosporins, 87–89

adverse effects, 88–89

agents, 87

cefdinir, 87

cefixime, 87

cefotaxime, 87

cefpodoxime, 87

ceftazidime, 87

ceftibuten, 87

ceftriaxone, 87

mechanism of action, 87

spectrum, 87

Thrombotic thrombocytopenic, HIV and, 236

Ticarcillin, 73

Tigecycline, 127

Tinidazole, 139

Tipranavir (TPV)

described, 259–263

Tissue, penetration of an antibiotic into

TMP. See Trimethoprim (TMP)

TMP/SMX. See Trimethoprim/sulfamethoxazole (TMP/SMX)

Tobramycin, 20, 124

described, 123

Total or actual body weight, 31

Toxicities, antibiotic, 44

Toxoplasma, 290

Trematodes, 290

Trimethoprim (TMP)

hematologic adverse effects of, 44, 156

Trimethoprim/sulfamethoxazole (TMP/SMX), 20, 33, 290

described, 155

susceptibility breakpoints, 38

Triumeq, 265–267

Trizivir, 249

Truvada, 249

Trypansoma, 290

U

Urinary tract infections (UTIs), 18

V

Vaccinia, 6

Valacyclovir

described, 235–237

HIV and, 236

Valganciclovir, 239–242

Vancomycin, 20, 21, 22, 41, 44

described, 107

Varicella-zoster virus (VZV), 4, 235–237

Varicella-zoster virus (VZV) agents

acyclovir, 235–237

adverse effects, 236

famciclovir, 235–237

mechanism of action, 235

valacyclovir, 235–237

Vertigo, 128

Vibrio, 12

Viridans streptococci, 9

Viruses, 3, 4

Vomiting, 250

Voriconazole, 20, 28, 33, 203

adverse effects, 214–215

central nervous system effects, 214

dermatologic effects, 214–215

dosing issues, 215

introduction of, 213

mechanism of action, 213

renal effects, 214

visual effects, 214

VZV. See Varicella-zoster virus (VZV)

W

Warfarin, 114, 140, 157

White blood cells (WBCs), 17

Y

Yeasts, 5, 192

Z

Zanamivir, 243–245

Zidovudine (ZDV, AZT), 251

described, 249–252

Zinc, 28

Z-max, 133

Z-pak, 133

Zygomycetes, 5