insulin lispro
Humalog, Liprolog, Lyumjev (previously Liumjev) · ATC code A10AB04;A10AD04
- Key facts
- Active substance
- insulin lispro
- Drug class
- Insulin analog
- ATC code
- A10AB04;A10AD04
- Authorisation
- centrally authorised across the EU (EMA)
- Dosage forms
- Humalog 100 units/ml solution for injection in vial / Humalog 100 units/ml solution for injection in cartridge / Humalog 100 units/ml KwikPen solution for injection in a pre-filled pen · Humalog Mix25 100 units/ml suspension for injection in vial / Humalog Mix25 100 units/ml suspension for injection in cartridge / Humalog Mix25 100 units/ml KwikPen suspension for injection in a pre-filled pen · Humalog Mix50 100 units/ml suspension for injection in cartridge / Humalog Mix50 100 units/ml KwikPen suspension for injection in a pre-filled pen · Humalog 200 units/ml KwikPen solution for injection in a pre-filled pen · Liprolog 100 units/ml, solution for injection in vial / Liprolog 100 units/ml, solution for injection in cartridge / Liprolog 100 units/ml KwikPen, solution for injection in a pre-filled pen · Liprolog Mix25 100 units/ml, suspension for injection in cartridge / Liprolog Mix25 100 units/ml KwikPen, suspension for injection in a pre-filled pen · Liprolog Mix50 100 units/ml, suspension for injection in cartridge / Liprolog Mix50 100 units/ml KwikPen, suspension for injection in a pre-filled pen · Liprolog 200 units/ml KwikPen, solution for injection in a pre-filled pen
- Marketing authorisation holder
- Eli Lilly Nederland B.V.
- Information as of
- 2026-10-27
Key facts
Insulin lispro is a rapid-acting human insulin analogue (e.g. Humalog, Liprolog, Lyumjev) for diabetes mellitus requiring insulin; the Mix25 and Mix50 forms combine it with an intermediate-acting component.
What it is used for
- Humalog/Liprolog: adults and children with diabetes mellitus requiring insulin, and initial stabilisation
- Humalog/Liprolog Mix25 and Mix50: diabetes mellitus requiring insulin
- Lyumjev 100 units/mL: diabetes mellitus in adults, adolescents and children aged 1 year and above; Lyumjev 200 units/mL in adults only
Dosing
- Dose determined by the physician according to the patient's requirement
- Humalog/Liprolog: shortly before meals, or soon after when necessary; duration of action 2 to 5 hours subcutaneously
- Lyumjev: zero to two minutes before the start of the meal, with the option of up to 20 minutes after starting
- Mix25/Mix50: subcutaneous injection only, never intravenously
- Humalog 100 units/ml may be given intravenously if necessary (e.g. ketoacidosis, perioperatively)
- Insulin requirements may be reduced in renal or hepatic impairment
- 200 units/ml: never transfer from the KwikPen to a syringe (risk of overdose)
Contraindications
- Hypersensitivity to the active substance or any excipient
- Hypoglycaemia
Important warnings
- Transfer to another insulin only under strict medical supervision; dose changes may be needed
- Risk of hypo- and hyperglycaemia; warning symptoms may be altered
- Combination with pioglitazone: cases of cardiac failure reported
- To avoid medication errors, check the insulin label before each injection
- Batch number should be recorded for traceability
Side effects
- Hypoglycaemia is the most frequent undesirable effect; severe hypoglycaemia may lead to loss of consciousness and, in extreme cases, death
- Local and systemic allergy
- Lipodystrophy and cutaneous amyloidosis at injection sites
Interactions
- Increased insulin requirement with e.g. oral contraceptives, corticosteroids, thyroid replacement, danazol, beta2 stimulants
- Reduced insulin requirement with e.g. oral hypoglycaemics, salicylates, sulpha antibiotics, MAOIs, SSRIs, ACE inhibitors, angiotensin II receptor blockers, beta-blockers, octreotide, alcohol
- Pioglitazone: consider the risk of cardiac failure
Pregnancy and breastfeeding
- No adverse effect on pregnancy indicated; insulin requirements usually fall in the first trimester and rise in the second and third
- Breast-feeding patients may need adjustments in insulin dose, diet or both
Summary of the official product information, written with AI (Claude, Anthropic) on 2026-10-28. Every number was checked automatically against the original text. Not reviewed by a physician – the full official text is authoritative.
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For patients
Package leaflet, verbatim
Authorisation and brand names by country
Medicines with exactly this active-substance composition, as listed in the national registers – alphabetical and without ranking. Whether a product is currently available is not shown here.
EU – centrally authorised (all member states)
- Bysumlog · biosimilarSandoz GmbH · EMEA/H/C/006158
- HumalogEli Lilly Nederland B.V. · EMEA/H/C/000088
- Insulin lispro Sanofi · biosimilarSanofi Winthrop Industrie · EMEA/H/C/004303
- LiprologEli Lilly Nederland B.V. · EMEA/H/C/000393
- Lyumjev (previously Liumjev)Eli Lilly Nederland B.V. · EMEA/H/C/005037
Source: European Medicines Agency (EMA), product information
Brand names in 3 more European countries
- Iceland
- Bysumlog, Humalog, Insulin Lispro, Liprolog, Lyumjev
- Liechtenstein
- Bysumlog, Humalog, Insulin Lispro, Liprolog, Lyumjev
- Norway
- Bysumlog, Humalog, Insulin Lispro, Liprolog, Lyumjev
EMA – Article 57 product data (EU/EEA), 2026-10-28
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Sources
- European Medicines Agency. Humalog – EPAR, Product Information (Detailed information on this medicinal product is available ). 2026-10-27. https://www.ema.europa.eu/en/documents/product-information/humalog-epar-product-information_en.pdf
- European Medicines Agency. Liprolog – EPAR, Product Information (Detailed information on this medicinal product is available ). 2026-10-27. https://www.ema.europa.eu/en/documents/product-information/liprolog-epar-product-information_en.pdf
- European Medicines Agency. Lyumjev (previously Liumjev) – EPAR, Product Information (OF THE TEXT Detailed information on this medicinal product i). 2026-10-27. https://www.ema.europa.eu/en/documents/product-information/lyumjev-epar-product-information_en.pdf
- Wikidata (CC0): ATC A10AB.
Editorial: Medelix editorial team · last updated 2026-10-27 · How these pages are made · Report an error
Source: European Medicines Agency (EMA), product information. Not advertising, not a treatment recommendation. For questions about your own treatment, ask your doctor or pharmacist.