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CHLOROQUINE TABLETS 250 MG [SIN01559P]
Active ingredients: CHLOROQUINE TABLETS 250 MG
Product Info
CHLOROQUINE TABLETS 250 MG
[SIN01559P]
Product information
Active Ingredient and Strength | CHLOROQUINE PHOSPHATE - 250 MG |
Dosage Form | TABLET, FILM COATED |
Manufacturer and Country | BEACONS PHARMACEUTICALS PTE. LTD. - SINGAPORE |
Registration Number | SIN01559P |
Licence Holder | BEACONS PHARMACEUTICALS PTE. LTD. |
Forensic Classification | PHARMACY ONLY MEDICINES |
Anatomical Therapeutic Chemical (ATC) code | P01BA01 |
THERAPEUTIC PROPERTIES:
Chloroquine is used for the suppression and treatment of malaria. It is especially active against the erythrocytic forms of malaria parasites. It is not active against tissue forms of the malaria parasites.
DOSAGE:
Suppression in adults: 500mg (300mg base) on the same day each week, beginning 2 weeks prior to exposure, continued for 4 – 8 weeks after leaving the area. If treatment begins on exposure, a loading dose of 1 gm can be taken in divided doses 6 hours apart.
Suppression in children: 5mg base/kg/week. The loading dose is 10mg base/kg/week.
Acute attacks in adults: an initial dose of 1 gm (600mg base), followed by 500mg (300mg base) after 6 to 8 hours and a single dose of 500mg (300mg base) on each of 2 consecutive days.
Table caption
For children: A total of 25mg / kg is given over 3 days. | First dose | : 10mg base/kg |
Second dose | : 5mg base/kg, 6 hours after the first dose | |
Third dose | : 5mg base/kg, 18 hours after the second dose | |
Fourth Dose | : 5mg base/kg, 24 hours after the third dose |
For a radical cure of vivax and malariae malaria, concomitant therapy with an 8-aminoquinoline compound like primaquine is necessary.
CONTRAINDICATIONS:
Chloroquine is contraindicated in the presence of retinal or visual field changes of any aetiology, in patients with psoriasis or porphyria, and in patients with known hypersensitivity to 4-aminoquinolines. However, the drug can be used in these cases in acute attacks of malaria if the physician elects to use it after carefully weighing the possible risks and benefits to the patient.
