HYPERIUM Tablet Ref.[51129] Active ingredients:

Source: Medicines Authority (MT)  Revision Year: 2021  Publisher: Les Laboratoires Servier, 50, rue Carnot, 92284 Suresnes cedex, France

4.1. Therapeutic indications

Hypertension.

4.2. Posology and method of administration

Posology

The recommended dosage is 1 tablet daily as a single morning dose.

In the event of insufficient results after one month of treatment, the dosage may be increased to 2 tablets daily in 2 doses (one in the morning and one in the evening) at the beginning of meals.

Given its good clinical and biological acceptability, Hyperium may be administered to elderly and diabetic patients.

Treatment may be continued indefinitely.

Patients with renal impairment

In patients with renal insufficiency, a dosage adjustment is in principle not necessary if the creatinine clearance is greater than 15 ml/min.

Paediatric population

Due to the lack of clinical experience, the use of Hyperium in children is not recommended.

4.9. Overdose

Symptoms

Data related to a massive ingestion are very limited. The most likely expected symptoms in this case would be marked hypotension and disorders of vigilance.

Management

The treatment must be symptomatic. In addition to gastric lavage, the recommended treatment may involve the use of sympathomimetics agents in case of marked hypotension. Hyperium is weakly dialyzable.

6.3. Shelf life

2 years.

6.4. Special precautions for storage

Do not store above 30°C.

6.5. Nature and contents of container

Boxes of 10, 15, 20 or 30 tablets in blister packs (Aluminium/Polyamide/PVC).

Not all pack sizes may be marketed.

6.6. Special precautions for disposal and other handling

No special requirements.

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