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LENAPAIN TABLETS
SCHEDULING STATUS:
S2
PROPRIETARY NAME
(and dosage form:)
LENAPAIN TABLETS
COMPOSITION:
Each tablet contains:
Doxylamine
Succinate 5,00 mg
Codeine
Phosphate
10,00 mg
Caffeine
, Anhydrous
30,00 mg
Paracetamol
450,00 mg
PHARMACOLOGICAL CLASSIFICATION:
A - 2.9 : Special analgesic combination
PHARMACOLOGICAL ACTION:
Lenapain tablets have analgesic, antipyretic and antihistaminic action.
INDICATIONS:
Relief of mild to moderate pain associated with tension.
CONTRA-INDICATIONS:
Sensitivity to any of the ingredients. The dosage in renal functional impairment must be reduced. Should be taken only
with caution by asthmatics. Severe liver function impairment. Lenapain should not be administered to patients with acute
intermittent porphyria. Asthma, respiratory depression especially in the presence of cyanosis and excessive bronchial
secretion, head injuries and conditions in which intracranial pressure is raised, heart failure secondary to chronic lung
disease, a history of cardiac disease, epilepsy, and all convulsive states, patients taking monoamine oxidase inhibitors or
within 14 days of stopping such treatment, acute alcoholism. Lenapain should not be taken during pregnancy, nor whilst
breast-feeding.
WARNINGS:
Dosages in excess of those recommended may cause severe liver damage. Patients suffering from liver or kidney
disease should take Paracetamol under medical supervision. Consult your doctor if no relief is obtained with the
recommended dosage. This medicine may lead to drowsiness and impaired concentration, which may be aggravated
by simultaneous intake of alcohol or other central nervous system depressant agents. Patients should be warned
against taking charge of vehicles or machinery and performing potentially hazardous tasks
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