Sepsis- My Drug Chart
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8/3/2019 Sepsis- My Drug Chart
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Echinocandin antifungals
Drug Indication/Dosage MOA CI Kinetics ADEs Misc
Anidulafungin (Eraxis) Candidemia, candidiasis of
esophagus, intra-abdominal and
peritonitis
Off-label: txt of Aspergillus
IV powder, IV only
Noncompetitive inhibitor of synthesis
of - (1,3)-D-glucagon of the cell wall;
decreased glucan content leads to
osmotic instability and cell lysis
Hypersensitivity Preg: C
PB: 84%
T1/2: 27hrs
Hypokalemia, diarrhea, DVT,
abnormal LFTs, hepatic necrosis,
seizure, histamine-mediated rxn
- do not a
-rate of i
1.1mg/m
-reconsti
then furt
Caspofungin (Cancidas) Txt of Aspergillus in refractory pts,candidemia, febrile neutropenia
IV powder, IV only
Inhibits synthesis of (1,3)-D-glucan, anessential component of the cell wall of
susceptible fungi. Highest activity in
regions of active cell growth.
Mammalian cells do not require (1,3)-
D-glucan, limiting potential toxicity.
hypersensitivity Preg: CPB: 97%
T1/2: 9-11hrs
Hypotension, rash, diarrhea,peripheral edema, tachycardia,
increased LFTs, complication of
infusion, fever, shivering, erythema
multiforme, SJS, pancreatitis,
hepatic necrosis, liver failure,
anaphylaxis, sepsis, septic shock,
Nephrotoxicity, renal impairment
pleural effusion, respiratory
distress, respiratory failure,
WBC, Hg, Hct, phlebitis, SCr
- dont m- admin s
admin as
- reconst
bacterios
- good ag
species
Micafungin (Mycamine) Esophageal candidiasis, Candida
prophylaxis is pts undergoing HSCT
Off-label: infxn due to Aspergillus
IV powder, IV only
semisynthetic lipopeptide
(echinocandin) synthesized by a
chemical modification of fermentation
product of Coleophoma empetri F-
11899, that inhibits the synthesis of 1,3
beta-D-glucan,a fundamental
constituent of fungal cell walls .
Hypersensitivity Preg: C
Substrate: 3A4 (minor)
Inhibits: 3A4 (weak)
PB: >99% to albumin
Metab: forms M-1
(catechol) and M-2
(methoxy)
T1/2: 11-21hrs
Febrile neutropenia, hemolytic
anemia, intravascular hemolysis,
neutropenia, thrombocytopenia,
hepatitis, renal impairment, drug-
induced anaphylaxis, D/N/V,
mucosal inflammation,
constipation, hypomagnesemia
- add NS
- infuse o
- flush ex
infusion
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Azole Antifungals
MOA: triazole antifungals that inhbit 14-alpha-demethylase ezyme needed to convert lanosterol to fecosterol in the biosynthesis of ergosterol. Depletes fungi of ergosterol. This means they cant construct their membranes prop
dividing and causing static activityDrug Indication/Dosage CI Kinetics ADEs Misc
Fluconazole (Diflucan) Candidiasis
Admin: IV, po
Dosage: IV sol, pow for susp, tablet
Hypersensitivity Preg: C
Inhibits: 2C9, 2C19, 3A4
PB: 11-12%
Bioavail: >90%
T1/2: 30hrs
N/V, LFTs, HA, torsades de
pointes, SJS, seizure, alopecia
(long term)
- shown resistance among C. albi
HIV pts
- C. glabrata less susceptibility
- max rate of infusion is 200mg/h
- high CNS penetration
Itraconazole (Sporanox)
BBW: Heart failure
BBW: high potential for
interactions
Candidiasis
Admin: IV, po
Dosage: capsule, solution
Concomitant use with 3A4 drugs,
hypersensitivity, pregnant women treating
onychomycosis,
Preg: C
Substrate: 3A4
Inhibits: 3A4, PGP
PB: 99.8%
Metab: 3A4 to hydroxy-
itraconazole
Rash, abnormal lipids, N, HA,
upper respiratory problems, CHF,
SJS, hepatoxicity, anaphylaxis
- Infuse over 1 hr
- after admin flush line with 15-20
over 30sec-15min
- Avoid pregnancy use contracept
post treatment
- low CNS penetration
Voriconazole (Vfend) Candidiasis
Admin: IV, po
Dosage: tablet, IV pow for sol, po
pow for sol
Concomitant use of carbamazepine, 3A4
substrates, ergot alkaloids, LA barbiturates,
St. Johns wort, rifampin, hypersensitivity
Preg: D
Substrate: 2C9, 2C19
Inhibits: 2C9, 3A4
PB: 58%
Metab: 2C19, 2C9, 3A4
Bioavial: 96%
Visual disturbances,
hallucinations, SJS/TEN,
pancreatitis, colored vision,
hepatoxicit, Creatinine increased
- High CNS penetration
- good against fluconazole resista
species
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Agent Contraindications Dosage/Admin Kinetics Adverse effects Pt. Counseling
Aztreonam
(Azactam, Cayston)
Rare cross-allergy to cephs and pens.
Use with caution in renal patients
Available as oral inhalation (Cayston), and IM/IV injection
Dosage: I.V.: 2 g every 6-8 hours; maximum: 8 g/day
Give in combo with levofloxacin or moxifloxacin, or
gatifloxacin, with or without aminoglycoside
Rash, N/V/D,
thrombophlebitis, pain at
injection site