Dosages
Side effects in children
Warnings & precautions in children
Contra-indications in children

Interactions
PK
Renal impairment
References

Fludarabine

Generic name
Fludarabine
Brand name
ATC Code
L01BB05

Pharmacokinetics in children

No information

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dose recommendation of formulary compared to licensed use (on-label versus off-label)

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Available formulations

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Dosages

Oncological conditions
  • Intravenous
    • 0 years up to 18 years
      • The dose and dosing frequency of cytostatic agents depend on the condition and are very much subject to new insights. Cytostatic drugs are mostly used in oncology and haematology in combinations. For this reason, please refer to the detailed treatment protocols; it is also the reason why no dose recommendations have been included.

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Renal impaiment in children > 3 months

at a creatinine clearance of > 50 ml/min/1.73m²
no dose adjustment required
at a creatinine clearance of 30-50 ml/min/1.73m²

50% of the normal dose, then dose depending on the blood counts
at a creatinine clearance of less than 30 ml/min/1.73m²
contraindicated (see below)

There are two case reports known in which a child with renal function of < 30 ml/min was successfully treated with fludarabine.
1. Heitink-Pollé 2008 (Wilhelmina Children’s Hospital, Utrecht)
Girl (5 yrs) with Fanconi anaemia, chronic renal impairment (creatinine clearance 22 ml/min/1.73m²). because of a bone marrow transplant: fludarabine at 15 mg/m² for 3 days + thoracoabdominal irradiation (not the kidneys). This was instead of the normal regimen: fludarabine at 30 mg/m² for 5 days + Cytoxan + ATG. Cytoxan was replaced because of the risk of toxicity in reduced renal function.
2. Turkistani 2010 (Saudi Arabia)
Girl (2 yrs) with Fanconi anaemia, chronic renal impairment (creatinine clearance estimated at 17 ml/min/1.73m² and 12 ml/min/1.73m² based on 24-hour urine). Because of a stem cell transplant: fludarabine at 15 mg/m² for 3 days + Cytoxan + ATG. This was instead of the normal regimen: fludarabine at 30 mg/m² for 5 days + Cytoxan + ATG. The Cytoxan was also adjusted because of the reduced renal function!

Information
In reduced renal function, the AUC of the active metabolite increases. The risk of side effects is elevated as a result.

Clinical consequences
Dose-related side effects include bone marrow depression (that can become severe), nausea (primarily in oral administration) and stomatitis.

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The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here

Side effects

No information is present at this moment.

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The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here

Contra-indications

No information available on specific contra indications in children.

The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here

Warnings & precautions in children

Extravasation: The nature of any reactions on extravasation is unknown.

General cytostatic: a range of cytostatics can trigger hypersensitivity reactions. An emergency set (containing epinephrine, clemastine and hydrocortisone) should be present in the treatment room. The emergency set also contains specific antidotes.

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Interactions

The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here

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Reference

  1. Rademaker C.M.A. et al, Geneesmiddelen-Formularium voor Kinderen, 2007

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Changes

Changes