Hylenex (Wydase, Amphadase, Vitrase, Hydase, hyaluronidase)
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Introduction
Tradenames: Wydase, Amphadase, Vitrase, Hydase, Hylenex (recominant)
Indications
- to increase the dispersion & absorption of other drugs
- increase the absorption of parenteral fluids given by hypodermoclysis
- enhance diffusion of locally irritating or toxic drugs in the management of IV extravasation
Contraindications
Caution:
- 0.02 mL intradermal test dose for sensitivity prior to administration
Dosage
- management of IV extravasation
- reconstitute 150 unit vial of lyophylized powder with mL of normal saline
- take 0.1 mL of this solution & dilute with 0.9 mL of normal saline to yield 15 units/mL
- five 0.2 mL injections are made SC or intradermally into the extravasation site at the leading edge using a 25 or 26 gauge needle
- change needle after each injection
- hypodermoclysis
- absorption & dispertion of drugs
- 150 units added to vehicle containing the drug
Injection: (lyophylized) 150 units
Injection: (solution) 150 units/mL (1 mL)
Amphadase, Hydase (bovine), Vitrase (ovine), Hylenex (human)
Adverse effects
- uncommon (< 1%)
Mechanism of action
- hyaluronoglucosaminidase (hyaluronidase)
More general terms
Additional terms
Component of
- hylenex/trastuzumab
- hylenex/ocrelizumab
- hylenex/immune globulin
- efgartigimod/hylenex
- daratumumab/hylenex
- atezolizumab/hylenex
References
- ↑ Kaiser Permanente Northern California Regional Drug Formulary, 1998
- ↑ Prescriber's Letter 12(2): 2005 New Drugs Approved by the FDA in 2004 Detail-Document#: http://prescribersletter.com/(5bhgn1a4ni4cyp2tvybwfh55)/pl/ArticleDD.aspx?li=1&st=1&cs=&s=PRL&pt=3&fpt=25&dd=210216&pb=PRL (subscription needed) http://www.prescribersletter.com