Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Daptomycin
Drug ID BADD_D00581
Description Daptomycin is a cyclic lipopeptide antibacterial agent with a broad spectrum of activity against Gram-positive bacteria, including methicillin-susceptible and -resistant _Staphylococcus aureus_ (MSSA/MRSA) and vancomycin-resistant Enterococci (VRE).[A231379, A231384, L32534] Chemically, daptomycin comprises 13 amino acids, including several non-standard and D-amino acids, with the C-terminal 10 amino acids forming an ester-linked ring and the N-terminal tryptophan covalently bonded to decanoic acid.[A231374, L32534] Daptomycin was first discovered in the early 1980s by researchers at Eli Lilly in soil samples from Mount Ararat in Turkey.[A231384] Early work on developing daptomycin was abandoned due to observed myopathy but was resumed in 1997 when Cubist Pharmaceuticals Inc. licensed daptomycin; it was found that a once-daily dosing scheme reduced side effects while retaining efficacy.[A231379] Daptomycin was approved by the FDA on September 12, 2003, and is marketed under the name CUBICIN? by Cubist Pharmaceuticals LLC (Merck & Co.).[L32534]
Indications and Usage For the treatment of complicated skin and skin structure infections caused by susceptible strains of Gram-positive microorganisms.
Marketing Status Prescription; Discontinued
ATC Code J01XX09
DrugBank ID DB00080
KEGG ID D01080
MeSH ID D017576
PubChem ID 16134395
TTD Drug ID D05HPI
NDC Product Code 71288-016; 0143-9378; 0703-0125; 0409-5933; 42513-0015; 16729-434; 67254-515; 73402-111; 31722-102; 0409-0122; 43598-413; 63323-585; 71288-017; 71839-107; 68225-082; 43598-476; 42513-0004; 72572-100; 69097-850; 0409-2757; 60977-145; 68225-052; 25021-174; 67919-012; 57885-0011; 25021-179; 72572-102; 69097-807; 70594-034; 51187-0002; 0409-0120; 67184-0549; 16714-892; 17337-0261; 60505-6229; 67457-813; 63323-871; 0781-3295; 71288-018; 16729-435; 63323-371; 68001-467; 68001-376; 55150-344; 70594-053; 71839-108; 67919-011
Synonyms Daptomycin | Deptomycin | Cubicin | Daptomycin, 9-L beta-Aspartic Acid | Daptomycin, 9 L beta Aspartic Acid | LY-146032 | LY 146032 | LY146032
Chemical Information
Molecular Formula C72H101N17O26
CAS Registry Number 103060-53-3
SMILES CCCCCCCCCC(=O)NC(CC1=CNC2=CC=CC=C21)C(=O)NC(CC(=O)N)C(=O)NC(CC(=O)O)C(=O)NC3C(OC (=O)C(NC(=O)C(NC(=O)C(NC(=O)CNC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)CNC3=O)CCCN)C C(=O)O)C)CC(=O)O)CO)C(C)CC(=O)O)CC(=O)C4=CC=CC=C4N)C
Chemical Structure
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal distension07.01.04.001--
Abdominal pain07.01.05.002--
Abscess11.01.08.0010.000319%Not Available
Acute myocardial infarction02.02.02.001; 24.04.04.001--Not Available
Acute respiratory distress syndrome22.01.03.0010.000555%
Acute respiratory failure14.01.04.004; 22.02.06.0010.000083%Not Available
Agranulocytosis01.02.03.0010.000532%Not Available
Alanine aminotransferase increased13.03.01.0030.000958%
Alveolitis allergic10.01.03.008; 22.01.01.0020.001384%Not Available
Anaemia01.03.02.001--
Anaphylactic reaction10.01.07.001; 24.06.03.0060.000532%
Anaphylactic shock10.01.07.002; 24.06.02.0040.000639%Not Available
Angioedema10.01.05.009; 23.04.01.001--Not Available
Anxiety19.06.02.002--
Aortic valve incompetence02.07.03.0010.000213%Not Available
Aphasia17.02.03.001; 19.21.01.001--
Arrhythmia02.03.02.001--Not Available
Arrhythmia supraventricular02.03.03.001--Not Available
Arthralgia15.01.02.001--
Ascites02.05.04.002; 07.07.01.001; 09.01.05.003--
Aspartate aminotransferase increased13.03.01.0060.001171%
Asthenia08.01.01.001--Not Available
Atrial fibrillation02.03.03.002--
Atrial flutter02.03.03.0030.000213%
Back pain15.03.04.005--
Bacteraemia11.01.11.0010.000305%
Bilirubin conjugated increased13.03.01.0070.000319%Not Available
Blindness unilateral06.02.02.009; 17.17.01.0160.000213%Not Available
Blister12.01.06.002; 23.03.01.001--Not Available
Blood bicarbonate increased13.11.01.001--Not Available
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