Pharmacokinetics in children
No information
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
| Juvenile idiopathic arthritis (JIA) and systemic lupus erythematodes (SLE) |
- Oral
-
1 month
up to
18 years
[2]
[3]
[4]
[5]
-
5
mg/kg/day
in 1
dose. Max: 400 mg/day.
Only on prescription or after consultation with a pediatric rheumatologist / immunologist
In individual cases it may be necessary to increase the dose to a maximum of 6.5 mg/kg/day, but only on prescription from a pediatric rheumatologist / immunologist and after balancing the risk of retinopathy with an increased (cumulative) dose of hydroxychloroquine against the possible insufficient effectiveness of a lower dosage.
|
| Prophylaxis for malaria |
- Oral
-
1 month
up to
18 years
[1]
|
| Treatment of uncomplicated malaria |
- Oral
-
1 month
up to
18 years
[1]
A total dose of up to 2000 mg is administered over 3 days, as follows: First dose: 13 mg/kg, maximum one-time dose of 800 mg Second dose: 6.5 mg/kg, max 400 mg/dose, 6 hours after first dose third dose: 6.5 mg/kg, max 400 mg/dose, 18 hours after second dose fourth dose: 6.5 mg/kg, max 400 mg/dose, 24 hours after third dose.
|
Renal impaiment in children > 3 months
Be cautious in patients with renal impairment. Dose adjustment may be needed.
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
Gastrointestinal complaints, skin abnormalities, hair loss, myopathy, dizziness, tinnitus, irreversibel retinopathy [ACR], hypoglycemia.
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 in children
Young children are particularly sensitive to 4-aminoquinoline derivatives and relatively small doses can cause very severe intoxication (such as fatal respiratory and circulatory insufficiency).
Hydroxychloroquine can prolong the QT interval: the extent of the prolongation of the QT time may increase with increasing concentration of hydroxychloroquine. Perform an ECG before starting treatment. Be cautious in congenital or documented acquired QT prolongation and / or known risk factors for QT prolongation.
When used in JIA: the therapeutic effect occurs only after a few weeks or months. In cases of severe side effects, the treatment must be discontinued.
Dosages above 5 mg/kg actual body weight have a higher risk for rethinopathy, especially when used longer than 5 years. The risk is also greatly increased in renal impairment (eGRF < 60 ml/min) and therefore the dose should be adjusted. Monitoring of plasmalevels (trough) is indicated.
Although evidence on retinopathiy in children is lacking, ophtalmologic examination in children is recommended before start of treatment and yearly thereafter. Treatment with hydroxychloroquine should be stopped immediately at first signs of retinal abnormalities or new interference with vision (including color vision).
Retinal abnormalities can show progress even after treatment termination.
Interactions
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
ANTIMALARIALS
This pages provides a list of drugs from the same ATC class for comparison. This does not necessarily mean that these drugs are interchangeable.
| Methanolquinolines |
|
|
|
P01BC02
|
|
|
|
P01BC01
|
| Diaminopyrimidines |
|
|
|
P01BD01
|
| Artemisinin and derivatives, plain |
|
|
|
P01BE03
|
| Artemisinin and derivatives, combinations |
|
|
|
P01BF01
|
References
-
Sanofi-Aventis Netherlands BV, SPC Plaquenil (RVG 00853) 17-03-2020, www.geneesmiddeleninformatiebank.nl
-
Franssen MJAM et al, Werkboek Kinderreumatologie, VU Uitgeverij, 2008, 2e druk
-
Sectie Kinderreumatologie/immunologie Nederlandse Vereniging voor Kindergeneeskunde, Expert opinion Hydroxychloroquine en rethinopathie, 2019, June
-
American college of Rheumatology (ACR) , Position statement Screening for Hydroxychloroquine Retinopathy, 2017
-
Nederlandse Vereniging voor Reumatologie, Standpunt HCQ Retinopathie screening, 2018, November
-
SWAB in collaboration with CIB, NVZA, NVMM, NVII and NVIC, Medicamenteuze behandelopties bij patiënten met COVID-19 (infecties met SARS-CoV-2), https://swab.nl/nl/covid-19, May, 1, 2020
-
Yao, X. et al , In Vitro Antiviral Activity and Projection of Optimized Dosing Design of Hydroxychloroquine for the Treatment of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), Clin Infect Dis., 2020 Mar 9. pii: ciaa237. doi: 10.1093/cid/ciaa237. [Epub ahead of print]
-
Magagnoli J, et al, Outcomes of hydroxychloroquine usage in united states veterans hospitalized with covid-19., Preprint, 2020
-
Perinel S, et al, Towards optimization of hydroxychloroquine dosing in intensive care unit COVID-19 patients, Clin Infect Dis, 2020
-
Chen Z, et al, Efficacy of hydroxychloroquine in patients with COVID-19: Results of a randomized clinical trial, Preprint, 2020
-
Mahévas M, et al, No evidence of clinical efficacy of hydroxychloroquine in patients hospitalised for COVID-19 infection and requiring oxygen: Results of a study using routinely collected data to emulate a target trial., Preprint, 2020
-
Tang W, et al, Hydroxychloroquine in patients with COVID-19: An open-label, randomized, controlled trial, Preprint, 2020
Therapeutic Drug Monitoring
Overdose