Medicine information EXJADE 500mg dispersible tablets

Product code:
W64442001
Quantity:
28
Indicated for:
iron overload
Route of administration:
oral
Substance:
deferasirox (chelating agent)
ATC
V03AC03 — Various | All other therapeutic products | All other therapeutic products | Iron chelating agents
Deferasirox is an iron chelator used for the treatment of chronic iron overload in patients with frequent blood transfusions, such as those with major thalassemia. It works by binding excess iron, facilitating its elimination through feces.

The medication is taken orally, usually once daily, with the dose adjusted based on the body's iron levels and the patient's weight. Common side effects include nausea, diarrhea, abdominal pain, and elevated liver enzymes.

Deferasirox is contraindicated in patients with severe renal impairment, hepatic failure, or hypersensitivity to the active substance. Its use also requires regular monitoring of renal and hepatic function.

This medication is an effective option for managing iron overload, helping to prevent complications associated with this condition.

General data about EXJADE 500mg

Substance:
deferasirox
Date of latest medicines list:
01-03-2022
Product code:
W64442001
Strength:
500mg
Pharmaceutical form:
dispersible tablets
Quantity:
28
Product type:
Original
Prescription status:
P-RF — Medicines dispensed with a medical prescription that is retained by the pharmacy and cannot be renewed.

Marketing authorisation

Manufacturer:
NOVARTIS PHARMA GMBH - GERMANIA
Holder:
NOVARTIS EUROPHARM LIMITED - IRLANDA
Number:
356/2006/05
Shelf life:
3 years

Pharmaceutical forms available for deferasirox

Strengths available for deferasirox

  • 125mg
  • 180mg
  • 250mg
  • 360mg
  • 500mg
  • 90mg

Official documents

The SmPC text is not displayed because a match to this medicine, strength and pharmaceutical form has not been confirmed.

The correspondence between the document and the displayed text is unconfirmed.

Source institution
EMA
Document language
English
Source record: first published
20/08/2009
Source record: last updated
05/02/2026