alglucosidase alfa (injection)
Generic Name: alglucosidase alfa (injection) (AL gloo KOE si dase AL fa)
Brand Name: Lumizyme, Myozyme
What is alglucosidase alfa?
Alglucosidase alfa contains an enzyme that naturally occurs in the body in healthy people. Some people lack this enzyme because of a genetic disorder. Alglucosidase alfa helps replace this missing enzyme in such people.
Alglucosidase alfa is used to treat a glycogen storage disorder called Pompe disease, (also called GAA deficiency) in adults and children who are at least 8 years old.
Alglucosidase alfa may also be used for purposes not listed in this medication guide.
What is the most important information I should know about alglucosidase alfa?
Some people receiving alglucosidase alfa have had serious allergic reactions during or shortly after infusion of this medicine. Tell your caregivers or get emergency medical help right away if you have any signs of a severe allergic reaction, such as itching, rash. redness or tingling, severe headache, feeling like you might pass out, fast or slow heart rate, wheezing, trouble breathing, pale skin, and blue lips or fingernails.
If you have heart disease or a breathing disorder, using alglucosidase alfa could make these conditions worse. Tell your doctor about all your medical conditions.
What should I discuss with my health care provider before receiving alglucosidase alfa?
You should not receive alglucosidase alfa if you are allergic to it.
To make sure alglucosidase alfa is safe for you, tell your doctor if you have:
lung disease or breathing disorder;
if you are allergic to mice, hamsters, or drug products made with "murine" proteins.
FDA pregnancy category C. It is not known whether alglucosidase alfa will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medicine.
Alglucosidase alfa can pass into breast milk and may harm a nursing baby. Do not breast-feed within 24 hours after receiving alglucosidase alfa. If you use a breast pump during this time, throw out any milk you collect. Do not feed it to your baby.
Your name may be listed on the Pompe Registry. This is to track the progress of your disease and the outcome of your treatment with alglucosidase alfa.
How is alglucosidase alfa given?
Alglucosidase alfa is injected into a vein through an IV. A healthcare provider will give you this injection. Alglucosidase alfa must be given slowly, and the IV infusion can take up to 4 hours to complete.
This medicine is usually given once every 2 weeks.
Before each injection, tell your doctor if you have recently been sick with a cold, flu, or other illness.
If you need surgery, tell the surgeon ahead of time that you are using alglucosidase alfa.
Alglucosidase alfa can have long lasting effects on your body. Your blood will need to be tested every 3 months for 2 years and then once every year after that.
What happens if I miss a dose?
Call your doctor for instructions if you miss an appointment for your alglucosidase alfa injection.
What happens if I overdose?
Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.
What should I avoid while receiving alglucosidase alfa?
Follow your doctor's instructions about any restrictions on food, beverages, or activity.
Alglucosidase alfa side effects
Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.
Some people receiving alglucosidase alfa have had serious allergic reactions when the medicine was injected into the vein, or as long as 3 hours afterward. Tell your caregivers or get emergency medical help right away if you have any of these signs of a severe allergic reaction:
feeling like you might pass out, even while lying down;
slow heart rate, weak pulse, fainting, slow breathing (breathing may stop);
bronchospasm (wheezing, tight feeling in your chest or throat, trouble breathing);
pale skin, cold or clammy skin, blue lips or fingernails, cold hands or feet;
warmth, redness, numbness, or tingly feeling under your skin;
rash, itching, sweating, fever;
severe headache, nausea, feeling restless or nervous;
seizure (convulsions); or
fast heart rate, pounding in your neck or ears, anxiety, confusion.
Also call your doctor at once if you have:
skin changes (sores, lesions, ulcers, discoloring); or
puffy eyes, swelling in your ankles or feet, weight gain, urine that looks foamy.
Common side effects may include:
pale skin, blue lips, feeling hot or feverish;
skin rash, flushing (warmth, redness, or tingly feeling);
headache, dizziness, agitation, muscle twitching;
fast heart rate, rapid breathing, chest discomfort, cough;
tremor, shaking, increased sweating; or
muscle pain, tiredness.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
Alglucosidase alfa dosing information
Usual Adult Dose for Pompe disease:
20 mg/kg via IV infusion every 2 weeks
-Total volume of infusion is determined by patient's body weight and should be infused over about 4 hours.
Usual Pediatric Dose for Pompe disease:
20 mg/kg via IV infusion every 2 weeks
-Total volume of infusion is determined by body weight and should be infused over about 4 hours.
What other drugs will affect alglucosidase alfa?
Other drugs may interact with alglucosidase alfa, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell each of your health care providers about all medicines you use now and any medicine you start or stop using.
See also: Side effects (in more detail)
More about alglucosidase alfa
- Side Effects
- During Pregnancy or Breastfeeding
- Dosage Information
- Support Group
- En Español
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- Drug class: lysosomal enzymes
Related treatment guides
Where can I get more information?
- Your doctor or pharmacist can provide more information about alglucosidase alfa.
- Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.
- Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.
Copyright 1996-2012 Cerner Multum, Inc. Version: 5.01.
Last reviewed: October 26, 2014
Date modified: October 13, 2017