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Mulpleta (Lusutrombopag): Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx)
Strength:
3 mg
Active ingredient:

Patient information: uses, side effects, how to take - Mulpleta

What is MULPLETA?

MULPLETA is a prescription medicine used to treat low platelet count (thrombocytopenia) in adults with chronic liver disease who are scheduled to have a procedure.

MULPLETA is not used to make platelet count normal in people with chronic liver disease.

It is not known if MULPLETA is safe and effective in children.

Before taking MULPLETA, tell your healthcare provider about all of your medical conditions,including if you:

  • have a blood clot or have had a history of a blood clot.
  • have any blood clotting problems, other than thrombocytopenia.
  • are pregnant or plan to become pregnant. MULPLETA may harm your baby.

  • are breastfeeding or plan to breastfeed. It is not known if MULPLETA passes into your breast milk. Do not breastfeed during your treatment with MULPLETA and for at least 28 days after your last dose. Talk to your healthcare provider about the best way to feed your baby during your treatment with MULPLETA.

Tell your healthcare provider about all the medicines you take,including prescription and over-the-counter medicines, vitamins, and herbal supplements.

How should I take MULPLETA?

  • Take MULPLETA exactly as your healthcare provider tells you to take it.
  • Your healthcare provider will tell you when to start taking MULPLETA.
  • Take MULPLETA 1 time each day for 7 days.
  • MULPLETA may be taken with or without food.

  • If you miss a dose of MULPLETA, take the missed dose as soon as possible on the same day and return to your normal schedule the following day.
  • If you take too much MULPLETA, call your healthcare provider or go to the nearest hospital emergency room right away.
  • Your healthcare provider will check your platelet count before you start treatment with MULPLETA and before your procedure.

What are the possible side effects of MULPLETA?

MULPLETA may cause serious side effects,including:

Blood clots,including blood clots in the liver, may happen in people with chronic liver disease and who take MULPLETA. You may have an increased risk of blood clots if you have certain blood clotting conditions.

The most common side effect of MULPLETAis headache.

These are not all of the possible side effects of MULPLETA.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

How should I store MULPLETA?

  • Store MULPLETA at room temperature between 68°F and 77°F (20°C to 25°C).
  • MULPLETA comes in a child-resistant blister pack. Keep MULPLETA in the packaging that it comes in.

Keep MULPLETA and all medicines out of the reach of children.

General information about the safe and effective use of MULPLETA.

Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use MULPLETA for a condition for which it was not prescribed. Do not give MULPLETA to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about MULPLETA that is written for healthcare professionals.

What are the ingredients of MULPLETA?

Active ingredient:lusutrombopag.

Inactive ingredients:D-mannitol, microcrystalline cellulose, magnesium oxide, sodium lauryl sulfate, hydroxypropyl cellulose, carboxymethylcellulose calcium, magnesium stearate, hypromellose, triethyl citrate, titanium dioxide, red ferric oxide, and talc.

Distributed by: Eddingpharm (U. S.) Inc., 220 Davidson Ave Ste 300A, Somerset, NJ 08873-4144, USA

For more information, go to www.mulpleta.comor call 1-888-465-2125.

About this document

Source: FDA drug labeling via NLM DailyMed · Application number: NDA 210923 · View the label on DailyMed

Revision date stated in the text: August 2025

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The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Mulpleta

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Active ingredient Lusutrombopag 3 mg
Dosage form Tablet, film coated
Route Oral
Marketing status listed in the FDA NDC Directory
Company (applicant) VANCOCIN ITALIA
FDA approval NDA 210923New Drug Application (NDA) Approved July 31, 2018
Reference listed drug This is the reference listed drug (RLD) that generics are compared with.
Manufacturers 3 labelers list this drug on DailyMed
Packages (NDC)
Package
3 mg – 7 in 1 dose pack / 1 in 1 carton NDC 85320-551-07

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.