Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Hyaluronidase (human recombinant)
Drug ID BADD_D01079
Description A purified preparation of the enzyme recombinant human hyaluronidase. Hyaluronidase (human recombinant) (INN Vorhyaluronidase alfa) is produced by genetically engineered Chinese Hamster Ovary (CHO) cells containing a DNA plasmid encoding for a soluble fragment of human hyaluronidase (PH20).[A4033] Hyaluronidase is an enzyme used to improve the absorption and dispersion of parenterally administered fluids, drugs, and contrast agents.[L13338] The action of hyaluronidase was first described in 1936, and named in 1939.[A199026] Early research into hyaluronidase identified it as a "spreading factor" which allowed for increased permeability of the connective tissue.[A199026] Hyaluronidase has been used in surgical settings for at least the past 60 years to improve the diffusion of local anesthetics.[A199047] Hyaluronidase was first used in prescription products in the United States on 5 May 2004.[L13338]
Indications and Usage Hyaluronidase is indicated for subcutaneous fluid administration for hydration, and increasing resorption of radiopaque agents in subcutaneous urography.[L13338] Hyaluronidase is also indicated by multiple routes to increase the dispersion of other injectable drugs.[L13338]
Marketing Status approved; investigational
ATC Code B06AA03
DrugBank ID DB06205
KEGG ID D04455; D06604; D04456
MeSH ID D006821
PubChem ID Not Available
TTD Drug ID Not Available
NDC Product Code 50090-4534; 18657-117
UNII 743QUY4VD8
Synonyms Hyaluronoglucosaminidase | Hyaluronidase | Hyaglosidase | Hyaluronate Hydrolase | Hydrolase, Hyaluronate | Duran-Reynals Permeability Factor | Duran Reynals Permeability Factor | Factor, Duran-Reynals Permeability | Permeability Factor, Duran-Reynals | GL Enzyme | Wydase
Chemical Information
Molecular Formula Not Available
CAS Registry Number 757971-58-7
SMILES Not Available
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Anaphylactic reaction24.06.03.006; 10.01.07.001--
Angioedema23.04.01.001; 10.01.05.009; 22.04.02.008--Not Available
Erythema23.03.06.001--Not Available
Hypersensitivity10.01.03.003--
Injection site reaction12.07.03.015; 08.02.03.014--
Oedema14.05.06.010; 08.01.07.006--Not Available
Pain08.01.08.004--
Urticaria23.04.02.001; 10.01.06.001--
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