국가: 남아프리카
언어: 영어
출처: South African Health Products Regulatory Authority (SAHPRA)
Lennon
DOLOROL® ELIXIR SCHEDULING STATUS: Not scheduled PROPRIETARY NAME (and dosage form): DOLOROL ® ELIXIR COMPOSITION: Each 5 mL contains: Paracetamol 120,00 mg Alcohol 9,5% v/v Preservative: Nipasept in a palatable flavoured base. 0,06% m/v This product contains Tartrazine. PHARMACOLOGICAL CLASSIFICATION: A 2.8 Non-Narcotic Analgesics, Antipyretics. PHARMACOLOGICAL ACTION: Paracetamol has analgesic and antipyretic effects similar to those of aspirin. However, it has no anti-inflammatory effect and does not share the antirheumatic properties of the salicylates. It is rapidly and practically completely absorbed from the gastro-intestinal tract. Plasma concentration reaches a peak in ½ to 1 hour; the plasma half-time is 1 to 3 hours. INDICATIONS: Paracetamol relieves pain and fever of moderate intensity. CONTRA-INDICATIONS: Severe liver function impairment. Sensitivity to paracetamol. WARNING: This product contains FD and C Yellow No. 5 (Tartrazine) which may cause allergic-type reactions (including bronchial asthma) in certain susceptible individuals. Although the overall incidence of Tartrazine sensitivity in the general population is currently thought to be low, it is frequently seen in patients who also have aspirin sensitivity. Dosage in excess of those recommended may cause severe liver damage. Patients suffering from liver or kidney disease should only take paracetamol under medical supervision. Consult your doctor if no relief is obtained from the recommended dosage. Do not use continuously for more than 10 days without consulting your doctor. DOSAGE AND DIRECTIONS FOR USE: 3 - 12 months ½ medicine measure (2,5 mL) in milk or water. 1 - 5 years 1 medicine measure (5 mL) 6 - 12 years 1 - 2 medicine measures (5 - 10 mL). The dose may be repeated every 4 hours, up to 4 t 전체 문서 읽기