Prednicarbat

Generic name
Prednicarbat
Brand name
ATC Code
D07AC18

Prednicarbat

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.

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

No information is present at this moment.

Available formulations

No information is present at this moment.

Dosages

Inflammatory dermatoses
  • Cutaneous
    • 1 month up to 18 years
        • Apply 1-2 times daily to affected skin using fingertip unit method.
        • Treatment duration: Up to 4 weeks

Renal impaiment in children > 3 months

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

Side effects

No information is present at this moment.

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.

Interactions

The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here

CORTICOSTEROIDS, PLAIN

This pages provides a list of drugs from the same ATC class for comparison. This does not necessarily mean that these drugs are interchangeable.

Corticosteroids, weak (group I)
D07AA02
Corticosteroids, moderately potent (group II)
D07AB01
D07AB02
D07AB09
Corticosteroids, potent (group III)
D07AC01
D07AC03
D07AC17
D07AC14
D07AC13
Corticosteroids, very potent (group IV)
D07AD01

References

  1. Sanofi-Aventis Deutschland GmbH, SmPC Dermatop® Creme 2,5 mg/g (5752.00.01), 08/2018
  2. Sanofi-Aventis Deutschland GmbH, SmPC Dermatop® Salbe 2,5 mg/g (5752.00.02), 08/2018
  3. Sanofi-Aventis Deutschland GmbH, SmPC Dermatop® Fettsalbe 2,5 mg/g (5752.00.00), 08/2018

Changes

Therapeutic Drug Monitoring


Overdose