What is the recommended dose of Xofluza (baloxavir marboxil) for an adult patient with a weight of 81kg?

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Xofluza Dosing for an 81kg Patient

For an 81kg patient, administer a single 80mg oral dose of Xofluza (baloxavir marboxil). 1

Weight-Based Dosing Algorithm

The FDA-approved dosing for Xofluza follows a clear weight-based threshold 1:

  • Patients weighing ≥80 kg: Single 80mg dose (one 80mg tablet) 1
  • Patients weighing 20 kg to <80 kg: Single 40mg dose (one 40mg tablet) 1

Since your patient weighs 81kg, they cross the 80kg threshold and require the higher 80mg dose. 1

Administration Timing and Guidelines

  • Administer as soon as possible within 48 hours of influenza symptom onset for treatment or following contact with an influenza-infected individual for post-exposure prophylaxis 1
  • Single dose only - no repeat dosing required 1
  • May be taken with or without food 1

Critical Administration Precautions

Avoid coadministration with the following, as they significantly reduce baloxavir absorption 1:

  • Dairy products 1
  • Calcium-fortified beverages 1
  • Polyvalent cation-containing laxatives 1
  • Antacids 1
  • Oral supplements containing calcium, iron, magnesium, selenium, or zinc 1

Dosing Consistency Across Indications

The American Academy of Pediatrics confirms that prophylaxis dosing is identical to treatment dosing - the same single 80mg dose applies whether treating active influenza or providing post-exposure prophylaxis in this weight category. 2, 3

Clinical Efficacy Context

High-quality evidence demonstrates that baloxavir 80mg in patients ≥80kg reduces time to symptom improvement by approximately 29 hours compared to placebo (median 73.2 vs 102.3 hours, p<0.0001), with efficacy similar to oseltamivir but with superior viral load reduction. 4 The single-dose regimen offers a significant adherence advantage over the 5-day twice-daily oseltamivir course. 4, 5, 6

Resistance Monitoring Caveat

Be aware that polymerase acidic protein variants with reduced baloxavir susceptibility emerged in approximately 5-10% of treated patients in clinical trials, particularly with influenza A(H3N2). 4, 7 However, this does not alter the initial dosing recommendation, though it underscores the importance of clinical follow-up if symptoms fail to improve. 4

References

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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