Dosages
Side effects in children
Warnings & precautions in children
Contra-indications in children

Interactions
PK
Renal impairment
References

Dengue vaccin

Generic name
Dengue vaccin
Brand name
ATC Code
J07BX04

Pharmacokinetics in children

Pharmacokinetic studies have not been performed

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dose recommendation of formulary compared to licensed use (on-label versus off-label)

No information is present at this moment.

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Available formulations

No information is present at this moment.

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Dosages

Active immunization against dengue
  • Subcutaneous
    • 4 years up to 18 years
      • 0.5 ml/dose 2 doses with a 3 month interval.

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Renal impaiment in children > 3 months

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

Side effects in children

Adverse reactions that were reported more frequently in children than in adults were fever (11% versus 3%), upper respiratory tract infection (11% versus 3%), nasopharyngitis (6% versus 0.6%), pharyngotonsillitis (2% versus 0.3%) and flu-like illness (1% versus 0.1%).

Adverse reactions reported less frequently in children than in adults were erythema at the injection site (2% versus 27%), nausea (0.03% versus 0.8%) and arthralgia (0.03% versus 1%)

In children < 6 years of age: Very often (>10%)   decreased appetite, drowsiness, irritability.

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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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Reference

  1. Takeda GmbH, SmPC Qdenga (EU/1/22/1699/001) 30-1-2023, www.ema.europa.eu

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Changes

Changes