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

Interactions
PK
Renal impairment
References

Glatirameer

Generic name
Glatirameer
Brand name
ATC Code
L03AX13

Pharmacokinetics in children

Er is geen informatie over de farmacokinetische parameters bij kinderen.

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

On-label

Licensed use Licensed use

Registration Status Title

Relapsing-remitting multipele sclerose (RRMS):
> 12 jaar: SC 20 mg/dag in 1 dosis

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Available formulations

Inj.vlst. (acetaat) 20 mg/ml; 40 mg/ml

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Dosages

Relapsing Remitting Multiple Sclerose (RRMS)
  • Subcutaneous
    • 12 years up to 18 years
      • 20 mg/day in 1 dose

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Renal impaiment in children > 3 months

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.

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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

Adult Side Effects

Zeer vaak (> 10%): reacties op de injectieplaats zoals overgevoeligheid, roodheid van de huid, pijn, zwelling, jeuk, ontsteking en oedeem; een 'Onmiddellijke (binnen enkele minuten optredende) Postinjectiereactie' met één of meer van de volgende systemische symptomen: vasodilatatie, pijn (op de borst), dyspneu, palpitaties of tachycardie. Misselijkheid, angst, depressie, hoofdpijn, griep, infectie, rugpijn, artralgie, asthenie.

Vaak (1-10%): bronchitis, herpes simplex, tandproblemen, cystitis, gastro-enteritis, otitis, rinitis, vaginale candidiasis, benigne neoplasma van de huid, lymfadenopathie, anorexie, gewichtstoename, nervositeit, smaakverandering, duizeligheid, slaperigheid, hypertonie, tremor, syncope, spraakstoornis, oog-, ooraandoening, hoest, constipatie, fecale incontinentie, braken, abnormale leverfunctietest, bloeduitstorting, hyperhidrose, jeuk, huidaandoening, mictiestoornis, urineretentie, rillingen, oedeem in het gezicht. Atrofie op de injectieplaats.

Soms (0,1-1%): abces, furunculosis, herpes zoster, pyelonefritis, huidcarcinoom, leukocytose, leukopenie, miltvergroting, trombocytopenie, struma, hyperthyreoïdie, alcoholintolerantie, jicht, hyperlipidemie, verhoogde natriumspiegel in het bloed, verlaagde serumferritinespiegel, abnormale dromen, euforie, hallucinatie, vijandigheid, manie, zelfmoordneiging, cognitieve stoornis, convulsie, dyslexie, spierkramp, nystagmus, stupor, gezichtsveldstoornis, oogbloeding, optische atrofie, droge ogen, extrasystolen, sinusbradycardie, spataderen, apneu, hyperventilatie, longaandoening, ademhalingsstoornis, (entero)colitis, oesofageale zweer, periodontitis, rectale bloeding, vergroting van de speekselklier, cholelithiasis, leververgroting, geneesmiddelgeïnduceerde leverbeschadiging en toxische hepatitis, angio-oedeem, erythema nodosum, artritis, bursitis, spieratrofie, osteoartritis, hematurie, nefrolithiase, urinewegaandoening, abortus, erectiestoornis, priapisme, prostaataandoening, gespannen borsten, vaginale bloeding, necrose op de injectieplaats, hypothermie.

Zelden (< 0,01–0,1%): anafylactische reacties, lipoatrofie, huidnecrose.

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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. TEVA GmBH, SmPC Copaxone (RVG 30086) 10-01-2019, www. geneesmiddeleninformatiebank.nl

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Changes

Changes