Uridine triacetate

From WikiMD's Food, Medicine & Wellness Encyclopedia

What is Uridine triacetate?[edit | edit source]


Uridine triacetate.svg
Uridine triacetate structure.svg



What are the uses of this medicine?[edit | edit source]


How does this medicine work?[edit | edit source]

  • Uridine triacetate is an acetylated form of uridine.
  • Following oral administration, uridine triacetate is deacetylated by nonspecific esterases present throughout the body, yielding uridine in the circulation


Who Should Not Use this medicine ?[edit | edit source]

  • This medicine have no usage limitations.


What drug interactions can this medicine cause?[edit | edit source]

  • No clinically important drug interactions have been observed with Xuriden.


Is this medicine FDA approved?[edit | edit source]

  • It was approved for use in the United States in 2015.


How should this medicine be used?[edit | edit source]

Recommended Dosage:

  • The recommended starting dosage of oral Xuriden is 60 mg/kg once daily.

Increase the dosage of Xuriden to 120 mg/kg (not to exceed 8 grams) once daily for insufficient efficacy, such as occurrence of one of the following:

  • Levels of orotic acid in urine remain above normal or increase above the usual or expected range for the patient
  • Laboratory values (e.g., red blood cell or white blood cell indices) affected by hereditary orotic aciduria show evidence of worsening
  • Worsening of other signs or symptoms of the disease

Administration

  • Measure the dose using either a scale accurate to at least 0.1 gram, or a graduated teaspoon, accurate to the fraction of the dose to be administered.
  • Once the measured dose has been removed from the Xuriden packet, discard the unused portion of granules.
  • Do not use any granules left in the open packet.

Administration with Food

  • Place 3 to 4 ounces of applesauce, pudding or yogurt in a small clean container.
  • Mix the measured amount of granules in the applesauce, pudding or yogurt
  • Swallow applesauce/pudding/yogurt immediately. Do not chew the granules. Do not save the applesauce/pudding/yogurt for later use.
  • Drink at least 4 ounces of water.

Administration in Milk or Infant Formula

  • Xuriden can be mixed with milk or infant formula instead of the soft foods described above for patients receiving up to 3/4 teaspoon (2 grams) of Xuriden. After weighing the dose of Xuriden:
  • Pour 5 mL of milk or infant formula into a 30 mL medicine cup.
  • Insert the tip of the oral syringe into the medicine cup and draw up 5 mL of milk/infant formula into the syringe.
  • Hold the syringe with the tip pointing upward. Pull down on the plunger until the plunger reaches 10 mL. This will add air to the syringe.
  • Place the cap over the tip of the syringe. Then invert the syringe so the syringe tip is pointing down, and remove the plunger.
  • Pour the measured amount of Xuriden granules into the syringe barrel and reinsert the syringe plunger. Do not push up on the plunger.
  • Gently swirl the syringe to mix the Xuriden granules with the liquid.
  • Turn the syringe so the syringe tip is pointing up. Then remove the syringe cap and push up on the plunger until the plunger reaches the 5 mL mark. This will remove air from the syringe.
  • Place the tip of the syringe in the patient's mouth between the cheek and gum at the back of the mouth. Gently push the plunger all the way down.
  • Refill the syringe with another 5 mL of milk/infant formula.
  • Gently swirl the syringe to rinse any remaining Xuriden granules from the syringe barrel.
  • Place the tip of the syringe in the patient's mouth between the cheek and gum at the back of the mouth. Gently push the plunger all the way down.
  • Follow with a bottle of milk or infant formula, if desired.


What are the dosage forms and brand names of this medicine?[edit | edit source]

This medicine is available in fallowing doasage form:

  • As Oral granules: 2 gram packets

This medicine is available in fallowing brand namesː

  • Xuriden


What side effects can this medication cause?[edit | edit source]

  • No adverse reactions were reported in clinical trials with Xuriden in patients with hereditary orotic aciduria.


What special precautions should I follow?[edit | edit source]

  • None


What to do in case of emergency/overdose?[edit | edit source]

  • In case of overdose, call the poison control helpline of your country. In the United States, call 1-800-222-1222.


Can this medicine be used in pregnancy?[edit | edit source]

  • There are no available data on Xuriden use in pregnant women to inform a drug-associated risk.


Can this medicine be used in children?[edit | edit source]

  • The safety and effectiveness of Xuriden have been established in pediatric patients.


What are the active and inactive ingredients in this medicine?[edit | edit source]

  • Active ingredient:

uridine triacetate

  • Inactive ingredients:

ORANGE JUICE HYPROMELLOSE, UNSPECIFIED POLYETHYLENE GLYCOL, UNSPECIFIED ETHYLCELLULOSE, UNSPECIFIED


Who manufactures and distributes this medicine?[edit | edit source]


What should I know about storage and disposal of this medication?[edit | edit source]

  • Store at controlled room temperature, 25°C (77°F); excursions permitted to 15° to 30°C (59° to 86°F).
Uridine triacetate Resources
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