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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
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