- Component of a multi-agent chemotherapeutic regimen for the treatment of patients with acute lymphoblastic leukemia in patients
- Reconstitute vial with 1 mL 0.9% NaCl to give a 10 000 unit/mL concentration. Preservative free.
- Caution: vigorous shaking may result in loss of potency. To mix, direct 0.9% NaCl to the side of the vial, then gently rotate the vial.
- Withdraw from vial within 15 minutes of reconstitution. Filter needle must be used.
- Stable in syringe or a mini-bag at room temperature for 4 hours
- Do not refrigerate syringe
- 0.9% NaCl
- Do not mix with other drugs
(For approved routes of administration by nursing personnel, refer to Policy for the Administration of Intravenous Medications.)
SC | NO |
IM | YES, inject into a large muscle. ***Maximum 2 mL per injection site*** |
IV Direct | YES |
IV Intermittent Infusion | YES, in 100mL 0.9% NaCl over 1 hour |
IV Continuous Infusion | NO |
(For neonatal dosages, refer to Neonatal IV Drug Manual.)
- 25 000 units/m2 , 3 times per week x 6 doses to replace each dose of Pegaspargase
- Dosage may differ according to protocol
Immediate (within a few minutes to hours):
- Anaphylaxis, other allergic reactions (6-43%) - urticaria, pruritus, respiratory distress, hypotension, chills, fever)
- Nausea and vomiting rare - more common with initial doses
- Pain/bruising at injection site (IM administration) - hold site at least 5 minutes after injection or until bleeding stops. Apply ice if platelet counts low.
Delayed (within a few days to weeks)
- Hemorrhagic and thrombotic cardiovascular events - decreased fibrinogen, clotting factors, antithrombin
- Hepatotoxicity - hypoalbuminemia, increased transaminases
- Hyperglycemia - monitor urine/blood glucose; hypoglycemia possible
- Pancreatitis - elevated serum amylase, assess for abdominal tenderness
- Myelosuppression
- Have anaphylaxis kit at bedside. Outpatients should remain in the clinic for at least one hour following injection. NOTE: anaphylaxis may be delayed following IM injection.
- Insulin may be required for severe hyperglycemia
-
Give asparaginase AFTER methotrexate, cytarabine and vincristine NOT BEFORE
- Erwinase Product Monograph (EUSA/Jazz Canada)
- Erwinase Product Monograph (Jazz-USA)
- COG Memo January 2, 2015 - Approval of IV route of Erwinia asparaginase
- Erwinia and Pegaspargase. Children’s Oncology Group. Parenteral and oral Chemotherapy Administration Guidelines used by the Children’s Oncology Group. Version 10.1 Version Date: 05/01/2020
- Erwinase Product Monograph (Jazz Pharmaceuticals France). Version 30 Aug 2016 (access 23 Feb2021 via HC product database website)