Based on population pharmacokinetic analysis, there was no clinically meaningful age-related difference in the pharmacokinetics of tezepelumab between adults and adolescents aged 12 to 17 years. The following pharmacokinetic parameters are known: (SmPC Tezspire)
| Tmax | 3 - 10 days (following a single subcutaneous administration) |
| Bioavailability (F) | 77% |
| Cl | 0,17 L/d* |
| Vd, central | 3,9 L* |
| Vd, peripheral | 2,2 L* |
| T1/2 | 26 days |
* based on population pharmacokinetic analysis for a 70 kg individual
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| Adjuvant treatment in severe asthma |
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No information available on dose adjustment in renal impairment.
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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
The safety profile in adolescents does not differ from that 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
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.
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The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
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| Xanthines | ||
|---|---|---|
| R03DA04 | ||
| Leukotriene receptor antagonists | ||
|---|---|---|
| R03DC03 | ||
| Other systemic drugs for obstructive airway diseases | ||
|---|---|---|
| R03DX09 | ||
| R03DX05 | ||
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