LuciBal (Baloxavir Marboxil)

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  • Model Number:
    RL50202506110902
  • Brand Name:
    LuciBal (Baloxavir Marboxil)
  • Origin:
    Generic drug,Laos
  • Small Orders:
    Small batches also available
  • Tags:
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Poster
  • Details
  • Description
  • Packaging Size
    4t/bottle/Box
  • Strength
    20mg
  • Compositon
    LuciBal (Baloxavir Marboxil)
  • Treatment
    influenza A and influenza B
  • Form
    Tablet
  • Brand
    LuciBal (Baloxavir Marboxil)
  • Quantity Unit
    20mg*4t/box
  • Manufacturer
    Lucius Pharmaceuticals (Lao) Co.,Ltd

About Baloxavir marboxil

Baloxavir marboxil is an antiviral medication used for the treatment of influenza A and influenza B. It can reduce the duration of flu symptoms by about 1-2 days in some people, but can also develop selection of resistant mutants that render it ineffectual; however studies noted this was seen mostly in children that were studied.

Influenza

Indications

  • Indicated for treatment of acute uncomplicated influenza in patients who have been symptomatic for ≤48 hr and who are otherwise healthy or at high risk of developing influenza-related complications
  • Indicated for postexposure prophylaxis of influenza following contact with an individual who has influenza

Dosage

  • Tablet or granules for oral suspension
    • <80 kg: 40 mg PO as a single dose
    • ≥80 kg: 80 mg PO as a single dose

Dosage Modifications

Coadministration with polyvalent cation-containing products

  • Avoid coadministration with dairy products, calcium-fortified beverages, polyvalent cation-containing laxatives or antacids, or oral supplements (eg, calcium, iron, magnesium, selenium, zinc)

Renal impairment

  • CrCl ≥50 mL/min: Pharmacokinetic analysis did not identify a clinically meaningful effect
  • Severe: Not studied

Hepatic impairment

  • Moderate (Child-Pugh B) to normal: No clinically meaningful pharmacokinetic differences were observed
  • Severe: Not studied

Dosing & Uses

AdultPediatric

Dosage Forms & Strengths

tablet

  • 40mg
  • 80mg

granules for oral suspension

  • 40mg/20mL bottle; reconstituted solution 2mg/mL
  • 30mg/packet
  • 40mg/packet
 

Influenza

Indications

  • Indicated for treatment of acute uncomplicated influenza in patients who have been symptomatic for ≤48 hr and who are otherwise healthy or at high risk of developing influenza-related complications
  • Indicated for postexposure prophylaxis of influenza following contact with an individual who has influenza

Dosage

  • Tablet or granules for oral suspension
    • <80 kg: 40 mg PO as a single dose
    • ≥80 kg: 80 mg PO as a single dose

Dosage Modifications

Coadministration with polyvalent cation-containing products

  • Avoid coadministration with dairy products, calcium-fortified beverages, polyvalent cation-containing laxatives or antacids, or oral supplements (eg, calcium, iron, magnesium, selenium, zinc)

Renal impairment

  • CrCl ≥50 mL/min: Pharmacokinetic analysis did not identify a clinically meaningful effect
  • Severe: Not studied

Hepatic impairment

  • Moderate (Child-Pugh B) to normal: No clinically meaningful pharmacokinetic differences were observed
  • Severe: Not studied
 

Dosing Considerations

Limitations of use

  • Influenza viruses change over time, and factors (eg, virus type or subtype, emergence of resistance, changes in viral virulence) could diminish drug’s clinical benefit
  • Check drug susceptibility patterns for circulating influenza virus strains

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