A study (n=6) with 1% cyclopentolate drops (35 µl) in the eye gave peak plasma concentrations ranging from undetectable to 5.8 ng/ml. Large inter-individual variability. Detectable levels from 3 minutes after administration in 5 children.
No information is present at this moment.
No information is present at this moment.
| Uveitis |
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| Diagnostic agent (cycloplegic) |
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GFR ≥10 ml/min/1.73m2: Dose adjustment not required.
GFR <10 ml/min/1.73m2: A general recommendation on dose adjustment cannot be provided.
The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Sleepiness or drowsiness (especially in young children (< 6 years) and in children with a low BMI), hyperactivity, red cheeks and dizziness.
Rare (0.1-0.01%): psychological disorders such as restlessness and speech and orientation disorders.
Also reported: epilepsy; necrotizing enterocolitis in premature neonates; Food intolerance in children.
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
Children (premature babies and infants in particular) are extra susceptible to side effects on the central nervous system and cardiovascular side effects. Try to limit systemic absorption as much as possible. Check children for signs of side effects for at least 30 minutes after administration. In young children and children with a low BMI, only use 1 drop of cyclopentolate if possible.
Particularly in (premature) neonates, food intolerance is reported after use of cyclopentolate drops. [Hermansen 1985; Chew 2005] In view of the pharmacodynamic effect on the motility of the gastrointestinal system and the occurrence of necrotising enterocolitis (NEC) in premature neonates in general, it is recommended that neonates be given no food for 4 hours after the examination.
Use with caution in children due to increased susceptibility to systemic anticholinergic side effects. Use caution if a severe systemic reaction has occurred in the past following atropine administration. Young children and children with Down's syndrome, spastic paralysis or brain damage are particularly susceptible to CNS disorders and to cardiopulmonary or gastrointestinal side effects. Also use caution in children with epilepsy. Children with fair skin and blue eyes may show an enhanced reaction and/or an increased sensitivity to side effects.
Hyperthermia: Use caution in patients, especially children, who have been exposed to elevated ambient temperatures or are febrile due to the potential for hyperthermia.
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.
| Anticholinergics | ||
|---|---|---|
| S01FA01 | ||
| S01FA05 | ||
| S01FA06 | ||