Regulatory Information
HSA regulatory responsibility and product classification details
Regulatory Responsibility
Product Classification
Formulation Information
TABLET, FILM COATED
**4.2 Posology and Method of Administration** Adults (including the elderly): The minimum effective dose should be employed. This dose should not exceed 6.5mg/kg/day (calculated from ideal body weight and not actual body weight) and will be either 200mg or 400mg per day. In patients able to receive 400mg daily: Initially 400mg daily in divided doses. The dose can be reduced to 200mg when no further improvement is evident. The maintenance dose should be increased to 400mg daily if the response lessens. Children: The minimum effective doses should be employed and should not exceed 6.5mg/kg/day based on ideal body weight. The 200mg tablet is therefore not suitable for use in children with an ideal body weight of less than 31 kg. Each dose should be taken with a meal or glass of milk. Hydroxychloroquine is cumulative in action and will require several weeks to exert its beneficial effects, whereas minor side effects may occur relatively early. For rheumatic disease, treatment should be discontinued if there is no improvement by 6 months. In light-sensitive diseases, treatment should only be given during periods of maximum exposure to light. The tablets are for oral administration.
ORAL
Medical Information
**4.1 Therapeutic Indications** Treatment of rheumatoid arthritis, juvenile chronic arthritis, discoid and systemic lupus erythematosus, and dermatological conditions caused or aggravated by sunlight.
**4.3 Contraindications** - Known hypersensitivity to 4-aminoquinoline compounds - Pre-existing maculopathy of the eye - Below 6 years of age (200 mg tablets not adapted for weight <35 kg) or for ideal body weight < 31 kg (see section 4.2)
Pending
xpending
Manufacturer Information
SANOFI-AVENTIS SINGAPORE PTE. LTD.
SANOFI AVENTIS, SA
Active Ingredients
Documents
Package Inserts
Plaquenil PI.pdf
Approved: March 7, 2022