The following pharmakokinetic parameters were observed in subjects with type 1 diabetes mellitus following the subcutaneous injection of glucagon (SmPC Ogluo):
| Age | 2-<6 years | 6-<12 years | 12-<18 years |
| Dosage | 0,5 mg | 0,5 mg | 1 mg |
| Cmax (mean) | 2300 pg/mL | 1600 pg/mL | 1900 pg/mL |
| tmax | 41 min | 34 min (median) | 51 min |
| AUC0-180min | 138900 pg/mL*min | 104700 pg/mL*min | 134300 pg/mL*min |
No information is present at this moment.
No information is present at this moment.
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| Diabetes, severe hypoglycaemia |
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| Diagnostic agent: determination of C-peptide (insulin reserve) |
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| Diagnostic agent: determination of hyperinsulinism |
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| Diagnostic agent: determination of GH/ACTH reserve |
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No information available on dose adjustment in renal impairment.
The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Injection for therapeutic use:
Very common: nausea
Common: hyperglycemia, vomiting, headache
[SmPC Ogluo]
The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
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
No information available on specific warnings and precautions in children.
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
This pages provides a list of drugs from the same ATC class for comparison. This does not necessarily mean that these drugs are interchangeable.