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ARTAMIN  ARTAMIN (CARDION)  CILAMIN  DISTAMIN 
 



Indication & Dosage
 
 
Oral
WILSON'S DISEASE
Adult: Doses titrated to maintain urinary copper excretion >2 mg/day. Patients should receive pyridoxine supplementation 25 mg/day. Initially, 1.5-2 g daily in divided doses. Maintenance dose: 0.75-1 g daily.
 
Oral
WILSON'S DISEASE
Child: 1 mth-12 yr: 2.5 mg/kg bid, increased every 1-2 wk to 10 mg/kg bid. 12-18 yr: 0.75-1 g bid, max: 2 g daily for 1 yr; usual maintenance 0.75-1 g daily. Doses titrated to maintain urinary copper excretion >2 mg/day. Patients should receive pyridoxine supplementation 25 mg/day. Elderly: Doses titrated to maintain urinary copper excretion >2 mg/day. Patients should receive pyridoxine supplementation 25 mg/day. Up to 20 mg/kg/day or 750 mg/day.
Max Dosage:  2 g daily for ≤ 1 yr.
 
Oral
CYSTINURIA
Adult: 1-4 g daily in 4 divided doses. Usual dose: 2 g/day. If 4 equal doses are not possible, give largest dose at bedtime. Doses adjusted to limit cystine excretion to 100-200 mg/day (<100 mg/day with history of stone formation). Patients should receive pyridoxine supplementation 25 mg/day.
 
Oral
CYSTINURIA
Adult: 1 mth-12 yr: 5-10 mg/kg bid, 12-18 yr: 0.5-1.5 g bid. Doses adjusted to limit cystine excretion to 100-200 mg/day (<100 mg/day with history of stone formation). Patients should receive pyridoxine supplementation 25 mg/day.
 
Oral
LEAD POISONING
Adult: 1-2 g daily in 3 divided doses. Continue treatment until urinary lead is stabilised at <500 mcg/day.
 
Oral
LEAD POISONING
Child: 20 mg/kg/day in 3 divided doses. Elderly: 20 mg/kg/day in 3 divided doses.
 
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SEVERE ACTIVE RHEUMATOID ARTHRITIS
Adult: As one part of a therapy programme. Initially 125-250 mg daily, increased gradually by the same amount at intervals of 4-12 wk up to 1-1.5 g/day. Discontinue if no response after 3-4 mth treatment with 1-1.5 g daily. Maintenance: 500-750 mg. Doses ≤500 mg/day: give as a single dose; doses > 500 mg: administer in divided doses. Max: 750 mg in older adults.
 
Oral
SEVERE ACTIVE RHEUMATOID ARTHRITIS
Child: As one part of a therapy programme. Initially, 3 mg/kg/day (≤250 mg/day for 3 mth, then 6 mg/kg/day (≤500 mg/day) bid for 3 mth. Max: 10 mg/kg/day in 3-4 divided doses (total max 750 mg/day). Elderly: As one part of a therapy programme. Initially 50-125 mg daily; max: 750 mg/day. Doses ≤500 mg/day: give as a single dose; doses > 500 mg: administer in divided doses.
Max Dosage:  Adult: 1.5 g/day. Elderly: 1 g/day.
 
Oral
CHRONIC ACTIVE HEPATITIS
Adult: Initially 500 mg daily in divided doses (after liver function tests shows disease controlled by corticosteroids). Dose gradually increased over 3 mth to 1250 mg daily with concurrent reduction in the corticosteroid dose. Elderly: Not recommended.
 
Oral
PREVENTION OF CYSTINE CALCULI
Adult: 0.5-1 g taken at bedtime.
 
Oral
PREVENTION OF CYSTINE CALCULI
Child: Use minimum dose required to maintain urinary cystine levels <200 mg/l. Elderly: Use minimum dose required to maintain urinary cystine levels <200 mg/l.
 
Oral
ARSENIC POISONING
Adult: 500 mg 4 times daily for 5 days.
 
Oral
ARSENIC POISONING
Adult: 100 mg/kg/day in divided doses 6 hrly for 5 days; max: 1g/day.
   
Administration Should be taken on an empty stomach (i.e. At least one hour before food or four hours after food). (Take on an empty stomach 1 hr before or 2 hr after meals, & at least 1 hr apart from any other drug, food, milk, antacid, Zn- or Fe-containing prep.)
   
Precautions Wilson's disease and cystinuria (25 mg/day) continued on a daily basis once instituted; renal impairment; penicillin allergy; monitor urine for proteinuria and hematuria, blood and platelet counts regurlarly; consider withdrawal if platelets fall <120000/mm3 or white blood cells <2500/mm3 or if 3 successive falls within reference range (reduce at reduced dose when levels are within reference range); withdraw permantly if leucopenia or thrombocytopenia reoccur. Regularly monitor renal and hepatic function (every 6 mths). Monitor body temperature twice weekly during 1st month of therapy, then every 2 wk for 5 mths, then monthly.
   
Potentially Life-threatening 
Adverse Drug Reactions
Nausea, anorexia, vomiting; oral ulceration and stomatitis; fever and skin reaction; loss of taste, thrombocytopaenia, neutropaenia, proteinuria, haematuria, haemolytic anaemia, lupus erythematosus-like syndrome, nephrotic syndrome; myasthenia gravis-like syndrome; goodpasture's syndrome. Stevens-Johnson-like syndrome.
   
Adverse Drug Reactions Agranulocytosis, aplastic anaemia; haematuria; Stevens-johnson syndrome.
   
Interactions Antacids, Iron and Zinc interfere with the absorption of penicillamine; concominant use of NSAIDs may increase risk of renal damage; may increase levodopa levels; may reduce serum digoxin levels.
   
   
 

 

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