What is this medicine?
IDURSULFASE (EYE dur SUL fase) is used to replace an enzyme that is missing in patients with Hunter syndrome. It is not a cure.
How should I use this medicine?
The medicine is for injection into a vein. It is given as an infusion by a health care professional in a hospital or clinic setting.
Contact your pediatrician or health care professional regarding the use of this medicine in children. While this drug may be prescribed for children as young as 16 months of age for selected conditions, precautions do apply.
What side effects may I notice from receiving this medicine?
Side effects that you should report to your doctor or health care professional as soon as possible:
allergic reactions like skin rash, itching or hives, swelling of the face, lips, or tongue
chest pain or tightness
dizziness; feeling faint or lightheaded, falls; unusually weak of tired
fast, irregular heartbeat
fever or chills
Side effects that usually do not require medical attention (report to your doctor or health care professional if they continue or are bothersome):
muscle or joint pain
What may interact with this medicine?
Interactions are not expected.
What if I miss a dose?
It is important not to miss your dose. Call your doctor or health care professional if you are unable to keep an appointment.
Where should I keep my medicine?
This drug is given in a hospital or clinic and will not be stored at home.
What should I tell my health care provider before I take this medicine?
They need to know if you have any of these conditions:
infection or fever
an unusual or allergic reaction to idursulfase, other medicines, foods, dyes, or preservatives
previous swelling of the tongue, face, or lips with difficulty breathing, difficulty swallowing, hoarseness, or tightening of the throat
pregnant or trying to get pregnant
What should I watch for while using this medicine?
Visit your doctor for regular check ups. Tell your doctor or healthcare professional if your symptoms do not start to get better or if they get worse.
You can be a part of a registry for patients with Hunter syndrome. This registry may ask for information over a long time. Ask your healthcare professional for more information.
July 17, 2018