VEIKIRIN Film-coated tablet Ref.[50615] Active ingredients: Amitriptyline

Source: Health Products Regulatory Authority (ZA)  Revision Year: 2022  Publisher: Strides Pharma SA (Pty) Ltd, 106 16th Road, Building 2, Midrand

4.1. Therapeutic indications

VEIKIRIN is indicated for the treatment of depression in adults (18 years and older).

4.2. Posology and method of administration

Posology

Adults

Initially 75 mg to 150 mg daily in divided doses.

Maintenance dose is 50 mg to 100 mg daily in divided doses.

Method of administration

Amitriptyline is for oral use.

The tablets should be swallowed with water.

4.9. Overdose

Overdosage and poisoning may be characterised by central nervous system depression or excitation, severe anticholinergic effects and cardiotoxicity. The signs and symptoms of an overdosage include: drowsiness, restlessness, ataxia, coma, stupor, cardiac dysrhythmias, pyrexia, palpitations, hypotension, tachycardia, convulsions and respiratory depression. Mixed poisoning with other central nervous system depressants is not uncommon. Treatment for overdosage is symptomatic and supportive.

6.3. Shelf life

2 years.

Store at or below 25°C.

6.4. Special precautions for storage

No special precautions for storage exist for VEIKIRIN.

6.5. Nature and contents of container

VEIKIRIN 10 are packed in PVC/PVdC/Aluminium blisters containing 30 film-coated tablets. The blister strips are packed in a printed carton.

VEIKIRIN 25 are packed in PVC/PVdC/Aluminium blisters containing 30 or 60 film-coated tablets. The blister strips are packed in a printed carton.

VEIKIRIN 50 are packed in PVC/PVdC/Aluminium blisters containing 30 film-coated tablets. The blister strips are packed in a printed carton.

Not all pack sizes may be marketed.

6.6. Special precautions for disposal and other handling

No special requirements.

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