Imiglucerase
Generic name: Imiglucerase
Brand names: Cerezyme
Dosage form: intravenous powder for injection (400 units)
Drug class:
Lysosomal enzymes
Usage of Imiglucerase
Imiglucerase is a man-made form of an enzyme that occurs naturally in the body. It is used as an enzyme replacement in people with Type I Gaucher disease.
Gaucher disease is a genetic condition in which the body lacks the enzyme needed to break down certain fatty materials (lipids). Lipids can build up in the body, causing symptoms such as easy bruising or bleeding, weakness, anemia, bone or joint pain, enlarged liver or spleen, or weakened bones that are easily fractured.
Imiglucerase may improve the condition of the liver, spleen, bones, and blood cells in people with Type I Gaucher disease. However, imiglucerase is not a cure for this condition.
Imiglucerase may also be used for purposes other than those listed in this medication guide.
Imiglucerase 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 side effects may occur during or shortly after the injection. Tell your caregiver right away if you feel dizzy, itchy, light-headed, sweaty, or have chest pain, cough, trouble breathing, or flushing (warmth, redness, or tingly feeling).
Imiglucerase may cause serious side effects. Call your doctor at once if you have:
Common side effects of imiglucerase may include:
Before taking Imiglucerase
You should not use imiglucerase if you are allergic to it.
To make sure imiglucerase is safe for you, tell your doctor if you have:
FDA pregnancy category C. It is not known whether imiglucerase will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using imiglucerase.
It is not known whether imiglucerase passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.
Imiglucerase should not be given to a child younger than 2 without a doctor's advice.
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- Pombiliti
- Sebelipase alfa
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- Vestronidase alfa
- Vestronidase alfa-vjbk
- Vimizim
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- Xenpozyme
How to use Imiglucerase
Usual Adult Dose for Gaucher Disease:
Initial dose: May range from 2.5 units/kg 3 times a week IV infusion to 60 units/kg IV infusion once every 2 weeksComments:-The majority of data available is for the 60 units/kg every 2 weeks dose.-Disease severity may dictate that treatment be initiated at a relatively high dose or relatively frequent administration.-Dose adjustments should be made on an individual basis and may increase or decrease based on achievement of therapeutic goals as assessed by routine evaluations of the patient's clinical manifestations.Use: For long-term enzyme replacement therapy in patients with a cOnfirmed diagnosis of Type 1 Gaucher disease that results in 1 or more of the following conditions: anemia, thrombocytopenia, bone disease, hepatomegaly, or splenomegaly
Usual Pediatric Dose for Gaucher Disease:
2 years or older:-Initial dose: May range from 2.5 units/kg 3 times a week IV infusion to 60 units/kg IV infusion once every 2 weeksComments:-The majority of data available is for the 60 units/kg every 2 weeks dose.-Disease severity may dictate that treatment be initiated at a relatively high dose or relatively frequent administration.-Dose adjustments should be made on an individual basis and may increase or decrease based on achievement of therapeutic goals as assessed by routine evaluations of the patient's clinical manifestations.Use: For long-term enzyme replacement therapy in patients with a confirmed diagnosis of Type 1 Gaucher disease that results in 1 or more of the following conditions: anemia, thrombocytopenia, bone disease, hepatomegaly, or splenomegaly
Warnings
Follow all directions on your medicine label and package. Tell each of your healthcare providers about all your medical conditions, allergies, and all medicines you use.
What other drugs will affect Imiglucerase
Other drugs may interact with imiglucerase, 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.
Disclaimer
Every effort has been made to ensure that the information provided by Drugslib.com is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Drugslib.com information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Drugslib.com does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Drugslib.com's drug information does not endorse drugs, diagnose patients or recommend therapy. Drugslib.com'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. Drugslib.com does not assume any responsibility for any aspect of healthcare administered with the aid of information Drugslib.com 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.
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