Plaquenil (Hydroxychloroquine) Dosing by Indication
Systemic Lupus Erythematosus and Lupus Nephritis
For SLE and lupus nephritis, hydroxychloroquine should be dosed at approximately 5 mg/kg/day based on actual body weight, not to exceed this threshold. 1
- The starting dose is around 5 mg/kg/day (typically 400 mg daily for most adults), with doses of 2-3 mg/kg/day potentially insufficient to achieve adequate blood levels and associated with higher flare rates 1
- Blood hydroxychloroquine levels above 0.6 mg/L may be associated with lower risk of lupus nephritis flare 1
- In patients with eGFR <30 mL/min per 1.73 m², reduce the dose by 25% 1
- The 2012 EULAR/ERA-EDTA guidelines recommend 6.5 mg/kg/day or 400 mg/day (whichever is lower) for patients with normal baseline ophthalmologic examination 1
- Keeping daily dosage <5.0 mg/kg actual body weight minimizes retinopathy risk while maintaining therapeutic efficacy 1
Rheumatoid Arthritis and Other Inflammatory Conditions
The standard dose for rheumatoid arthritis is 400 mg daily (200 mg twice daily), calculated to remain ≤5.0 mg/kg actual body weight. 1
- For patients of short stature, calculate dose based on actual body weight to avoid overdosage 1
- A loading dose of 600 mg/day may be used initially, with maintenance dosage calculated to remain below 6.5 mg/kg/day 2
Dermatomyositis and Juvenile Dermatomyositis
Hydroxychloroquine is administered at 200 mg twice daily (5 mg/kg) primarily for cutaneous manifestations. 1
- This dosing applies to both adult dermatomyositis and juvenile dermatomyositis 1
- For non-responders to hydroxychloroquine, chloroquine can be substituted at 250-500 mg/day 1
Malaria Treatment
For uncomplicated P. vivax or P. ovale malaria, give 4 tablets (800 mg salt) initially, then 2 tablets (400 mg salt) at 6,24, and 48 hours. 1
- This regimen is first-line treatment for chloroquine-sensitive malaria 1
- For chloroquine-resistant P. vivax, use artemisinin-based combination therapies instead 1
Critical Dosing Considerations
Renal Impairment
- Hydroxychloroquine is cleared primarily by the kidney, making renal disease a major risk factor for toxicity 1
- Reduce dose by 25% when eGFR <30 mL/min per 1.73 m² 1
- Patients with renal insufficiency require lower doses and closer monitoring 1
Body Weight Calculations
- Always use actual body weight, not ideal body weight, for dose calculations 1
- The risk of retinopathy is statistically similar across BMI groups ranging from 15-35 kg/m² when dosed by actual body weight 1
- Using ideal body weight formulas results in overdosage in thin individuals 1
Retinopathy Risk Stratification
- Doses >5.0 mg/kg dramatically increase both population risk and annual incremental risk of retinopathy 1
- At recommended doses ≤5.0 mg/kg, retinopathy risk is <2% during the first 10 years and increases to approximately 4% after 20 years 1
- Doses of 6-8 mg/kg carry substantially higher risk, with 21.6% cumulative incidence at 15 years for doses >6 mg/kg versus 2.7% for doses ≤5 mg/kg 3
Monitoring Requirements
- Baseline ophthalmologic examination is no longer required before initiating treatment 1
- Annual ophthalmologic screening should begin after 1 year in patients with risk factors (concomitant tamoxifen, eGFR <60 mL/min, dose >5 mg/kg/day, chloroquine use) or after 5 years otherwise 1
- G6PD testing is preferred in men of African, Asian, or Middle Eastern origin before starting treatment, though hemolysis risk appears low 1