Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Insulin lispro
Drug ID BADD_D01165
Description Insulin lispro is a rapid-acting form of insulin used for the treatment of hyperglycemia caused by Type 1 and Type 2 Diabetes. Insulin is prescribed for the management of diabetes mellitus to mimic the activity of endogenously produced human insulin, a peptide hormone produced by beta cells of the pancreas that promotes glucose metabolism. Insulin is released from the pancreas following a meal to promote the uptake of glucose from the blood into internal organs and tissues such as the liver, fat cells, and skeletal muscle. Absorption of glucose into cells allows for its transformation into glycogen or fat for storage. Insulin also inhibits hepatic glucose production, enhances protein synthesis, and inhibits lipolysis and proteolysis among many other functions.
Indications and Usage Insulin lispro is indicated to improve glycemic control in adults and children with diabetes mellitus.
Marketing Status approved
ATC Code A10AB04; A10AC04; A10AD04
DrugBank ID DB00046
KEGG ID D04477
MeSH ID D061268
PubChem ID 16132438
TTD Drug ID D0L6JE
NDC Product Code 0002-0535; 0002-1455; 0002-6007; 0002-7714; 0002-0120; 0002-0121; 0002-8797; 0002-2499; 0002-7511; 0002-8222; 0002-8233; 0002-7712; 0002-8798; 0002-8799; 0024-5926; 0002-7512; 0002-7752; 0002-0124; 0002-0137; 62381-7393; 62381-9516; 50090-1375; 50090-1663; 0002-7516; 62381-7516; 0110-0541; 0024-5924; 0024-5925; 0002-7737; 0110-0571; 62381-7662; 0002-8213; 0002-1099; 0002-2576; 62381-7394; 0002-7510; 50090-5391
UNII GFX7QIS1II
Synonyms Insulin Lispro | Lispro, Insulin | 28(B)-Lys-29(B)-Pro-Insulin | 28(B)-Lysine-29(B)-Prolineinsulin | Insulin, Lysyl(28B)-Prolyl(28B)- | Lispro | LYSPRO | Insulin, Lys(28B)-Pro(29B)- | Humalog Kwikpen | Kwikpen, Humalog | Humalog
Chemical Information
Molecular Formula C257H389N65O77S6
CAS Registry Number 133107-64-9
SMILES CCC(C)C(C(=O)NC(C(C)C)C(=O)NC(CCC(=O)O)C(=O)NC(CCC(=O)N)C(=O)NC(CS)C(=O)NC(CS)C( =O)NC(C(C)O)C(=O)NC(CO)C(=O)NC(C(C)CC)C(=O)NC(CS)C(=O)NC(CO)C(=O)NC(CC(C)C)C(=O) NC(CC1=CC=C(C=C1)O)C(=O)NC(CCC(=O)N)C(=O)NC(CC(C)C)C(=O)NC(CCC(=O)O)C(=O)NC(CC(= O)N)C(=O)NC(CC2=CC=C(C=C2)O)C(=O)NC(CS)C(=O)NC(CC(=O)N)C(=O)O)NC(=O)CN.CC(C)CC(C (=O)NC(CC1=CC=C(C=C1)O)C(=O)NC(CC(C)C)C(=O)NC(C(C)C)C(=O)NC(CS)C(=O)NCC(=O)NC(CC C(=O)O)C(=O)NC(CCCNC(=N)N)C(=O)NCC(=O)NC(CC2=CC=CC=C2)C(=O)NC(CC3=CC=CC=C3)C(=O) NC(CC4=CC=C(C=C4)O)C(=O)NC(C(C)O)C(=O)NC(CCCCN)C(=O)N5CCCC5C(=O)NC(C(C)O)C(=O)O) NC(=O)C(C)NC(=O)C(CCC(=O)O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC6=CN=CN6)NC(=O )C(CO)NC(=O)CNC(=O)C(CS)NC(=O)C(CC(C)C)NC(=O)C(CC7=CN=CN7)NC(=O)C(CCC(=O)N)NC(=O )C(CC(=O)N)NC(=O)C(C(C)C)NC(=O)C(CC8=CC=CC=C8)N
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)
Loss of consciousness17.02.04.004--Not Available
Medication error12.09.02.003--Not Available
Myalgia15.05.02.001--
Nausea07.01.07.001--
Neuropathy peripheral17.09.03.003--Not Available
Oedema14.05.06.010; 08.01.07.006--Not Available
Oedema peripheral14.05.06.011; 08.01.07.007; 02.05.04.007--
Pain08.01.08.004--
Pharyngitis22.07.03.004; 11.01.13.003; 07.05.07.004--
Pruritus23.03.12.001--
Pyrexia08.05.02.003--
Rash23.03.13.001--Not Available
Refraction disorder06.02.04.004--Not Available
Respiratory paralysis17.01.04.010; 22.02.06.003--Not Available
Retinal disorder06.08.03.005--Not Available
Rhinitis22.07.03.006; 11.01.13.004--
Seizure17.12.03.001--
Surgery25.01.02.003--Not Available
Swelling08.01.03.015--Not Available
Tachycardia02.03.02.007--Not Available
Urinary tract infection20.08.02.001; 11.01.14.004--
Ventricular arrhythmia02.03.04.006--
Weight increased13.15.01.006--
Wheezing22.03.01.009--
Infusion site erythema23.03.06.016; 12.07.05.009; 08.02.05.008--Not Available
Lipodystrophy acquired23.07.01.003; 14.08.04.008--Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Infusion site reaction12.07.05.006; 08.02.05.005--Not Available
Antibody test positive13.06.03.001--Not Available
Obstruction08.01.03.023--Not Available
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