Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Albumin microspheres (human)
Drug ID BADD_D00055
Description Human serum albumin is the primary protein present in human blood plasma. The main function of albumin is to maintain the oncotic pressure of blood [A33706]. It binds to water, cations (such as Ca2+, Na+ and K+), fatty acids, hormones, bilirubin, thyroxine (T4) and pharmaceuticals (including barbiturates). Albumin represents approximately 50% of the total protein content in healthy humans [A40060]. Human albumin is a small globular protein (molecular weight: 66.5 kDa), consisting of a single chain of 585 amino acids organized in three repeated homolog domains (sites I, II, and III). Each domain comprises two separate sub-domains (A and B) [A40060]. There are various preparations of albumin that are well established and widely available in the clinical setting [L3108], [L3109], [L3101]. Also known as _Albuminex_ 5% or 25%, one brand of human serum albumin is prepared from the pooled plasma of US donors in FDA-licensed facilities in the US [F229]. This is a biosimilar drug to existing human serum albumin and was approved for a biological license at both 5% and 25% concentrations by the FDA on June 21, 2018 [L3101].
Indications and Usage For treatment of severe blood loss, hypervolemia, and hypoproteinemia.
Marketing Status Not Available
ATC Code Not Available
DrugBank ID DB00062
KEGG ID Not Available
MeSH ID D012709
PubChem ID Not Available
TTD Drug ID Not Available
NDC Product Code 0944-0495; 64208-2510; 68982-633; 0944-0493; 68982-623; 68982-643; 64208-2512
Synonyms Serum Albumin | Albumin, Serum | Plasma Albumin
Chemical Information
Molecular Formula Not Available
CAS Registry Number 9048-46-8
SMILES Not Available
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Pruritus23.03.12.001--
Rash23.03.13.001--Not Available
Respiratory distress22.02.01.012--Not Available
Seizure17.12.03.001--
Tinnitus04.04.01.002; 17.04.07.004--
Tremor17.01.06.002--
Urticaria23.04.02.001; 10.01.06.001--
Ventricular extrasystoles02.03.04.007--Not Available
Visual acuity reduced17.17.01.011; 06.02.03.001--
Vomiting07.01.07.003--
Wheezing22.03.01.009--
Injection site discomfort12.07.03.019; 08.02.03.018--Not Available
Induration08.01.03.020--Not Available
Neurological symptom17.02.05.010--Not Available
The 2th Page    First    Pre   2    Total 2 Pages