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This drug may cause drowsiness, dizziness and psychomotor impairment in some patients which may seriously affect ability to perform hazardous activities requiring mental or physical alertness. Patients should not drive, use machinery and perform any hazardous activities during administration of the drug.
Should not be used concomitantly with alcohol or alcohol containing beverages.
It has been used only under the direction of a clinician in children under one year of age; patients with narrow angle glaucoma, prostatic hypertrophy or urinary retention.
It should be used with caution in pregnancy especially first trimester and lactation.
Do not exceed the recommended dose, overdosage may cause hepatotoxicity and do not continue use more than 5 days.
Avoid using this medicine with any other drug containing paracetamol. It may cause overdosage.
Patients with liver disease or renal disease or drinking alcoholic, should ask a physician or pharmacist before using this medicine.
If the symptom of swelling of the face; eyelid; lips; urticaria, faint, skin rash usually erythematous; maculopapular and toxic epidermal necrolysis have developed, the drug should be discontinued and consult a physician.
It has adverse effects include dryness of mouth, urinary retention, thickening of bronchial secretions, blurred vision, dizziness, nervousness and blood dyscrasia.
Pediatric and geriatric patients may be particularly susceptible to dizziness, sedation, delirium, dryness of mouth, urinary retention, hypotension, restlessness, insomnia and some patient may experience paradoxical reactions characterized by even seizures.
If it is used concomitantly with other depressant drugs such as benzodiazepines, anticholinergic drugs and antidepressants, caution should be exercised.
It should be used with caution in patients with hypertension, cardiovascular diseases, hyperthyroidism, experience of asthma and bronchiectasis.
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