ACUPAN Tablet Ref.[27918] Active ingredients: Nefopam

Source: Medicines and Medical Devices Safety Authority (NZ)  Revision Year: 2018  Publisher: iNova Pharmaceuticals (New Zealand) Limited, c/- Simpson Grierson, 88 Shortland Street, Auckland 1141

4.1. Therapeutic indications

ACUPAN is indicated for the relief of acute pain, including post-operative, dental, musculoskeletal and acute traumatic pain.

4.2. Posology and method of administration

Adults

Dosage may range from 1 to 3 tablets three times daily depending on response. The recommended starting dosage is 2 tablets three times daily.

Children

ACUPAN is not recommended for children under the age of 12 years.

Elderly

Elderly patients may require reduced dosage due to slower metabolism. It is strongly recommended that the starting dose does not exceed one tablet three times daily as the elderly appear more susceptible to, in particular, the CNS side effects of nefopam. Some cases of hallucination and confusion have been reported in this age group.

4.9. Overdose

Symptoms and Signs

Nefopam toxicity is manifested by neurological symptoms (coma, convulsions, hallucinations, agitation) and cardiovascular response (tachycardia with a hyperdynamic circulation).

Treatment

Supportive treatment is suggested including forced emesis and diuresis. Oral administration of activated charcoal may help prevent absorption. Convulsions and hallucinations should be controlled (e.g. with diazepam IV or pr). Beta-adrenergic blockers may be of use in controlling the cardiovascular complications.

For advice on the management of overdose please contact the National Poisons Centre on 0800 POISON (0800 764766).

6.3. Shelf life

5 years.

6.4. Special precautions for storage

Store below 25°C.

6.5. Nature and contents of container

Blister foil packs of 90 tablets.

6.6. Special precautions for disposal and other handling

None.

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