Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Albumin (human)
Drug ID BADD_D00054
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 B05AA01
DrugBank ID DB00062
KEGG ID D02792
MeSH ID D000075462
PubChem ID Not Available
TTD Drug ID D0I0VI
NDC Product Code 68516-5214; 68516-5216; 13533-692; 13533-691; 76125-790; 68516-5215; 76125-791; 76179-025; 61953-0002; 13533-690; 0053-7680; 44206-310; 44206-251; 76125-792; 61953-0001
Synonyms Serum Albumin, Human | Albumin, Human Serum | Human Serum Albumin | Albumin Human | Human, Albumin | Human Albumin | Albumin, Human
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)
Anaphylactic shock24.06.02.004; 10.01.07.002--Not Available
Angioedema10.01.05.009; 23.04.01.001--Not Available
Bradycardia02.03.02.002--Not Available
Cardiac failure02.05.01.001--
Cardiac failure congestive02.05.01.002--Not Available
Chills15.05.03.016; 08.01.09.001--
Circulatory collapse24.06.02.001--Not Available
Confusional state17.02.03.005; 19.13.01.001--
Dyspnoea22.02.01.004; 02.01.03.002--
Flushing24.03.01.002; 23.06.05.003; 08.01.03.025--
Headache17.14.01.001--
Hyperhidrosis08.01.03.028; 23.02.03.004--
Hypersensitivity10.01.03.003--
Hypertension24.08.02.001--
Hypotension24.06.03.002--
Loss of consciousness17.02.04.004--Not Available
Nausea07.01.07.001--
Pruritus23.03.12.001--
Pulmonary oedema02.05.02.003; 22.01.03.003--
Pyrexia08.05.02.003--
Rash erythematous23.03.06.003--Not Available
Tachycardia02.03.02.007--Not Available
Urticaria23.04.02.001; 10.01.06.001--
Vomiting07.01.07.003--
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