PERAZODIN Coated tablet Ref.[28192] Active ingredients: Dipyridamole

Source: Υπουργείο Υγείας (CY)  Revision Year: 2016  Publisher: Remedica Ltd, Aharnon Str., Limassol Industrial Estate, 3056 Limassol, Cyprus

4.1. Therapeutic indications

An adjunct to oral anti-coagulation for prophylaxis of thrombo-embolism associated with prosthetic heart valves.

4.2. Posology and method of administration

Posology

Adults

300-600 mg daily in three or four doses.

Children

Perazodin is not recommended for children.

Perazodin should usually be taken before meals.

Method of administration

Oral administration.

4.9. Overdose

Symptoms

Due to the low number of observations, experience with dipyridamole overdose is limited. Symptoms such as a warm feeling, flushes, sweating, restlessness, feeling of weakness, dizziness and anginal complaints can be expected. A drop in blood pressure and tachycardia might be observed.

Therapy

Symptomatic therapy is recommended. Administration of xanthine derivatives (e.g. aminophylline) may reverse the haemodynamic effects of dipyridamole overdose. Due to its wide distribution to tissues and its predominantly hepatic elimination, dipyridamole is not likely to be accessible to enhanced removal procedures.

6.3. Shelf life

5 years.

6.4. Special precautions for storage

Store below 25°C. Protected from light and moisture.

6.5. Nature and contents of container

Perazodin 25 mg coated tablets:

PVC/Aluminium blisters. Pack sizes of 100 and 1000 coated tablets.

PP containers with PE closure. Pack size of 1000 coated tablets

Perazodin 75 mg coated tablets:

PVC/Aluminium blisters. Pack sizes of 20, 30, 100 and 1000 coated tablets.

Perazodin 100 mg coated tablets:

PVC/Aluminium blisters. Pack sizes of 30, 100 and 1000 coated tablets.

6.6. Special precautions for disposal and other handling

No special requirements.

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