II. Indications
- Conditions
- Prevention of Invasive Aspergillus or Candida
- Oropharyngeal Candidiasis (including resistant to Itraconazole or Fluconazole)
- Invasive pulmonary Aspergillosis (off-label)
- Activity (similar activity to Voriconazole)
- Aspergillus species
- Blastomyces dermatitidis
- Candida (most species, including Fluconazole resistant strains)
- Coccidioides immitis
- Cryptococcus neoformans
- Dermatophytes or Tinea (Microsporum, Epidermophyton, Trichophyton)
- Histoplasma capsulatum
- Scedosporium apiospermum
- Mucorales or Zygomycetes (e.g. Mucor species, Rhizopus species)
- Other azoles (including Voriconazole) have no significant activity against Mucorales
III. Contraindications
- See Drug Interactions below
- Age <13 years
- Posaconazole Intravenous formulation if GFR <50 ml
- Resistant organisms
- Fusarium (variable activity)
IV. Mechanism
-
Azole Antifungal
- Second generation triazole
- Structurally similar to Itraconazole
- Inhibits fungal CYP450 enzymes
- Inhibits fungal sterol demethylation (selectively and strongly at 14-alpha demethylase)
- Blocks the synthesis of plasma membrane steroids (conversion from lanosterol to ergosterol)
- Results in plasma membrane damage
V. Medications
- Oral Delayed Release Tablets: 100 mg
- Take with food
- Do not split, crush or chew
- Oral Suspension: 40 mg/ml
- Take within 20 minutes of a meal
- Intravenous formulation: 300 mg/16.7 ml vials
- First dose may be administered by peripheral IV ove 30 minutes
- Subsequent doses should be via Central Line or PICC Line
- Posaconazole's IV vehicle may accumulate in renal Impairment (GFR<50 ml/min)
VI. Dosing: Adults (and children age >13 years)
- Prevention of Invasive Aspergillus or Candida
- Continued during period of severe Neutropenia or Immunosuppression
- Suspension
- Take 200 mg (5 ml) of suspension orally three times daily
- Delayed-Release Tablets
- Load 300 mg orally twice daily for first day
- Next, Take 300 mg orally daily
- Injection
- Load 300 mg IV over 30 to 90 minutes (peripheral, PICC or Central Line) every 12 hours for first day
- Next, infuse 300 mg IV over 90 minutes via Central Line or PICC every 24 hours
- Oropharyngeal Candidiasis
- Load suspension 100 mg (2.5 ml) orally within 20 minutes of a meal twice daily on first day
- Next, take suspension 100 mg (2.5 ml) orally within 20 minutes of a meal daily for 13 days
- Resistant Oropharyngeal Candidiasis (refractory to Itraconazole or Fluconazole, IDSA guidelines)
- Load suspension 400 mg (10 ml) orally within 20 minutes of a meal twice daily for 3 days
- Next, take suspension 400 mg (10 ml) orally within 20 minutes of a meal daily for up to 28 days
- Invasive pulmonary Aspergillosis (off-label, in adults)
- Take 200 mg (5 ml) suspension orally four times daily until stable
- Next, take 400 mg (10 ml) suspension orally twice daily for at least 6 to 12 weeks
- Continued throughout Immunosuppression and until lesions resolve
VII. Adverse Effects
- Common
- Uncommon
- Serious (rare)
- QTc Prolongation (Torsades de Pointes risk)
- Toxic Epidermal Necrolysis
- Angioedema
- Anaphylaxis
- Hematologic
- Case reports when combined with Cyclosporine or Tacrolimus in Transplant Rejection
- Hemolytic Uremic Syndrome
- Thrombotic Thrombocytopenic Purpura
VIII. Safety
- Avoid in Lactation
- Pregnancy
- Avoid in first trimester
- Skeletal malformations have been seen in animal studies
- Unknown safety after first trimester
IX. Pharmacokinetics
- Oral Bioavailability
- Significantly increased absorption and drug levels (up to 4 fold) when taken with a fatty meal
- Alternatives if meals (including Nutritional Supplements) are not tolerated
- Take with a carbonated beverage (e.g. Ginger ale)
- Switch to delayed release tablet
-
Elimination Half-Life: 20 to 66 hours
- Oral suspension levels >800 mg/day are unlikely to offer any additional benefit
- Protein Binding: High
- Metabolism
- UDP Glucuronidation
- P-gp Substrate and Inhibitor
- CYP3A4 Inhibitor (strong)
- Excretion
- Stool: 71%
- Urine: 13%
X. Drug Interactions
- Agents that prolong QTc Interval (risk of Torsades de Pointes)
- See Prolonged QT Interval due to Medication
- Avoid CYP3A4 substrates that prolong QTc Interval
- Pimozide
- Quinidine
- Agents that decrease oral suspension absorption (not delayed release tablets)
- Cimetidine
- Other H2 Blockers and Antacids do not appear affected
- Proton Pump Inhibitors
- Metoclopramide
- Cimetidine
- Other drugs that decrease Posaconazole levels
- Posaconazole increases other drug levels
- Posaconazole is a strong CYP3A4 Inhibitor
- Atazanavir
- Benzodiazepines
- Cyclosporine
- Decrease Cyclosporine doses by 25% and monitor levels
- Phenytoin
- Rifabutin
- Ritonavir
- Sirolimus
- Tacrolimus
- Decrease Tacrolimus doses by 66% and monitor levels
- Vinca Alkaloids
- Consider decreasing Vinca Alkaloid dose (or avoiding coadministration)
- Other drugs that are contraindicated with Posaconazole
- Ergot Alkaloids
- Halofantrine
- Statins
XI. Monitoring
XII. Resources
- Posaconazole Tablet (DailyMed)
- Posaconazole Suspension (DailyMed)
- Posaconazole Delayed Release Tablet (DailyMed)
XIII. References
- Hamilton (2020) Tarascon Pocket Pharmacopoeia
- (2012) Med Lett Drugs Ther 10(120): 61-8 [PubMed]
- (2006) Med Lett Drugs Ther 48(1248): 93-6 [PubMed]
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POSACONAZOLE DR 100 MG TABLET | Generic | $9.60 each |