- Dosages
- Side effects in children
- Warnings & precautions in children
- Contra-indications in children
-
Interactions - PK
- Renal impairment
- References
Pharmacokinetics in children
No information is present at this moment.
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dose recommendation of formulary compared to licensed use (on-label versus off-label)
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Available formulations
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Dosages
| Diabetes mellitus, insulin-dependent |
|---|
|
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Renal impaiment in children > 3 months
The insulin requirement may be decreased in cases of reduced renal function. The dosage is adjusted depending on the blood glucose measurements in this case.
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The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Side effects in children
Side effects in children are similar to side effects in adults. Injection site lipodystrophy is seen more often in children than in adults.
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The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
Contra-indications
No information available on specific contra indications in children.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
Warnings & precautions
No information available on specific warnings and precautions in children.
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Interactions
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
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| Insulins and analogues for injection, fast-acting | ||
|---|---|---|
| A10AB01 | ||
| Insulins and analogues for injection, intermediate-acting | ||
|---|---|---|
| A10AC01 | ||
| Insulins and analogues for injection, intermediate- or long-acting combined with fast-acting | ||
|---|---|---|
| A10AD06 | ||
| A10AD01 | ||
| Insulins and analogues for injection, long-acting | ||
|---|---|---|
| A10AE | ||
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References
- Rademaker C.M.A. et al, Geneesmiddelen-Formularium voor Kinderen, 2007
- Novo Nordisk A/S, SPC Novorapid (EU/1/99/119/001;008; 015) 03-02-2016, www.ema.europa.eu, http://www.ema.europa.eu/docs/nl_NL/document_library/EPAR_-_Product_Information/human/000258/WC500030372.pdf
- Sanofi-Aventis Deutschland GmbH, SPC Apidra (EU/1/04/285/001-004) 26-04-2010, www.geneesmiddeleninformatiebank.nl
- Eli Lily Nederland BV, SPC Humalog (EU/1/96/007/008) 28-10-2014, www.geneesmiddeleninformatiebank.nl
- Novo Nordisk A/S, SmPC Fiasp (EU 1/16/1160/001-011)26-08-2019
- Informatorium Medicamentorum, (Interacties), Geraadpleegd 16 juni 2016
- ZorgInstituut Nederand, Farmacotherapeutisch Kompas (Eigenschappen, Contra-Indicaties, Bijwerkingen, Waarschuwingen en Voorzorgen), Geraadpleegd 16 juni 2016
- Informatorium Medicamentorum, (Interacties), Geraadpleegd 16 juni 2016
- ZorgInstituut Nederand, Farmacotherapeutisch Kompas (Eigenschappen, Contra-Indicaties, Bijwerkingen, Waarschuwingen en Voorzorgen), Geraadpleegd 16 juni 2016
- ZorgInstituut Nederand, Farmacotherapeutisch Kompas (Eigenschappen, Contra-Indicaties, Bijwerkingen, Waarschuwingen en Voorzorgen), Geraadpleegd 16 juni 2016
- Informatorium Medicamentorum, (Interacties), Geraadpleegd 16 juni 2016
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Changes
Changes
