Insulin lispro
Insulin — ALIMENTARY TRACT AND METABOLISM
Also known as: humalog, humalog lispro, insulin lispro BS, insulin lispro protamine, insulin lispro protamine recombinant, insulin lispro recombinant, lyumjev
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Insulin lispro is a drug in the Insulin class catalogued in DrugCentral. It was first approved by the EMA in 1996. DrugCentral lists 1 molecular target, including INSR. Recorded indications include Diabetes mellitus type 1 and Diabetes mellitus type 2.
- Drug class: Insulin; Insulin Analog.
- Molecular targets: INSR (1 listed in DrugCentral).
- Indications: Diabetes mellitus type 1 and Diabetes mellitus type 2.
- ATC code: A10AB04 (Insulins and analogues for injection, fast-acting).
- Molecular formula: C257H383N65O77S6; molecular weight 5807.63 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (2)
- Diabetes mellitus type 1
- Diabetes mellitus type 2
Mechanism & targets
| Established pharmacologic class | Insulin; Insulin Analog |
|---|
Molecular targets (1)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Insulin receptor | INSR | agonist | — |
Regulatory approvals (3)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2020-03-25 | PMDA | — | Eli Lilly Japan K.K. | |
| 1996-06-14 | FDA | — | LILLY | |
| 1996-04-30 | EMA | — | Eli Lilly Nederland B.V. |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
A10AB04 | ALIMENTARY TRACT AND METABOLISM › DRUGS USED IN DIABETES › INSULINS AND ANALOGUES › Insulins and analogues for injection, fast-acting |
A10AC04 | ALIMENTARY TRACT AND METABOLISM › DRUGS USED IN DIABETES › INSULINS AND ANALOGUES › Insulins and analogues for injection, intermediate-acting |
A10AD04 | ALIMENTARY TRACT AND METABOLISM › DRUGS USED IN DIABETES › INSULINS AND ANALOGUES › Insulins and analogues for injection, intermediate- or long-acting combined with fast-acting |
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Blood glucose increased | 5592.4 |
| Hypoglycaemia | 3210.5 |
| Blood glucose decreased | 1267.6 |
| Diabetic ketoacidosis | 1179.7 |
| Diabetes mellitus inadequate control | 1027.3 |
| Hyperglycaemia | 948.2 |
| Product storage error | 902.4 |
| Blood glucose abnormal | 814.1 |
| Glycosylated haemoglobin increased | 767.8 |
| No adverse event | 606.5 |
| Incorrect dose administered | 584.4 |
| Blood glucose fluctuation | 505.2 |
Chemical structure
| Molecular formula | C257H383N65O77S6 |
|---|---|
| Molecular weight | 5807.63 g/mol |
| CAS number | 133107-64-9 |
| InChIKey | — |
| PubChem CID | 118984375 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Insulin lispro used for?
DrugCentral lists the following indications for Insulin lispro: Diabetes mellitus type 1 and Diabetes mellitus type 2.
How does Insulin lispro work?
Its molecular targets in DrugCentral include INSR (agonist).
When was Insulin lispro first approved?
Insulin lispro was first approved by the EMA in 1996.
What drug class does Insulin lispro belong to?
Insulin lispro is in the Insulin class.
What is the chemical formula of Insulin lispro?
Insulin lispro has the molecular formula C257H383N65O77S6 and a molecular weight of 5807.63 g/mol.
Browse: all drugs starting with I · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 5002 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1201538 — compound record and bioactivity
- PubChem CID 118984375 — chemical identifiers
- DrugBank DB00030 — drug record
- FDA UNII GFX7QIS1II — substance identity
- DailyMed: FDA labels for Insulin lispro — current prescribing information (label search)
- UniProt P06213 (INSR) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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