Source: Health Products Regulatory Authority (ZA) Revision Year: 2018 Publisher: Bayer (Pty) Ltd, 27 Wrench Road, Isando, 1600, SOUTH AFRICA 1968/011192/07 +27 11 921 5000
CLARITYNE is indicated for the relief of symptoms associated with perennial and/or seasonal allergic rhinitis, chronic urticaria and other allergic skin disorders.
For oral use only.
CLARITYNE can be taken with or without meal.
Body Weight equal to or less than 30 kg: 5 ml (1 medicine measure) once daily.
Body Weight more than 30 kg: 10 ml (2 medicine measures) once daily.
10 ml (2 medicine measures) once daily.
One tablet once daily.
Refer to “Side Effects”.
Somnolence, tachycardia and headache have been reported with overdoses. In the event of overdosage, treatment should be started immediately.
Treatment is symptomatic and supportive.
Consider standard measures to remove any unabsorbed medicine in the stomach, such as adsorption by activated charcoal administered as a slurry with water. The administration of gastric lavage should be considered.
0,9% Sodium chloride solution is the lavage solution of choice, particularly in children.
In adults tap water can be used; however, as much as possible of the amount administered should be removed before the next instillation. Sodium chloride or saline cathartics draw water into the bowel by osmosis and therefore, may be valuable for their action in rapid dilution of bowel content. Loratadine is not cleared by haemodialysis to any appreciable extent. After emergency treatment, the patient should continue to be medically monitored.
Store at or below 25°C.
Do not freeze.
Keep out of reach of children.
CLARITYNE Tablets: Protect from moisture.
CLARITYNE Syrup: Bottles of 100 ml.
CLARITYNE Tablets: Blister packs of 10 and 30 tablets.
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