On 7 May 1997, the European Commission issued a Marketing Authorisation valid throughout the European Union for the medicinal product Liprolog, which contains insulin lispro. The pharmaceutical company responsible for this medicinal product is Eli Lilly and Company Ltd. On 7 December 2000, the Marketing Authorisation holder notified the European Commission about the Marketing Authorisation holder's decision to withdraw the Marketing Authorisation for Liprolog. On 19 February 2001, the European Commission has adopted the decision withdrawing the Marketing Authorisation for the medicinal product for human use, Liprolog - insulin lispro EU 1/97/038/001-003. Pursuant to this decision the European Public Assesment Report for Liprolog has been removed from this website. For information, it should be noted that at present there is still a Marketing Authorisation valid throughout the European Union for the medicinal product Humalog, which contains insulin lispro. The pharmaceutical company responsible for this medicinal product is Eli Lilly and Company Ltd. Following a later application by the company, the European Commission [granted a marketing authorisation](/node/66998) for the medicine.
Therapeutic Indication
### Therapeutic indication For the treatment of patients with diabetes mellitus who require insulin for the maintenance of normal glucose homeostasis. Liprolog is also indicated for the initial stabilization of diabetes mellitus. Liprolog is a short acting insulin and may be used in conjunction with a longer acting human insulin. Liprolog is indicated for preprandial administration.
Therapeutic Area (MeSH)
ATC Code
A10AB04
ATC Item
insulin lispro
Pharmacotherapeutic Group
Drugs used in diabetes
Active Substance (Summary)
INN / Common Names
| Substance | CAS | Monograph |
|---|---|---|
| insulin lispro | N/A | 重组赖脯胰岛素 |
EMA Name
Liprolog
Medicine Name
Liprolog
Aliases
N/ANo risk management plan link.