NICARLOL ® PLUS - CÔNG TY CỔ PHẦN GLOBAL PHARMACEUTICAL

NICARLOL ® PLUS - CÔNG TY CỔ PHẦN GLOBAL PHARMACEUTICAL

NICARLOL ® PLUS - CÔNG TY CỔ PHẦN GLOBAL PHARMACEUTICAL

NICARLOL ® PLUS - CÔNG TY CỔ PHẦN GLOBAL PHARMACEUTICAL

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GLOBAL PHARMACEUTICAL JOINT-STOCK COMPANY

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NICARLOL ® PLUS
NICARLOL ® PLUS

NICARLOL ® PLUS

Present

Box of 3 blisters x 10 film-coated caplets

Ingredient

Nebivolol (as Nebivolol hydroclorid) 5mg. Hydroclorothiazid 12,5mg. Excipients q.s for 1 film-coated caplets

Point

Treatment of essential hypertension
   
DETAIL

NICARLOL ® PLUS

Keep out of reach of children. Read the manual carefully before use

If need more information please consult with your doctor

THERAPEUTIC INDICATION:

Treatment of essential hypertension.

POSOLOGY AND METHOD OF ADMINISTRATION:

Posology:

Adults

The dose is one tablet (5 mg/12.5 mg) daily, preferably at the same time of the day. Tablets may be taken with meals.

Elderly:  In view of the limited experience in patients above 75 years, caution must be exercised and these patients monitored closely

Renal impairment : Should not be given to patients with severe renal insufficiency

Hepatic impairment:  Data in patients with hepatic insufficiency or impaired liver function are limited. Therefore the use of Nicarlol in these patients is contraindicated.

Paediatric population:  The efficacy and safety of Nicarlol in children and adolescents aged below 18 years has not been established. No data are available. Therefore, use in children and adolescents is not recommended.

Method of administration:

Oral use. Tablets may be taken with meals

CONTRAINDICATIONS:

Hypersensitivity to the active substances or to any of the excipients

 Hypersensitivity to other sulphonamide-derived substances (since hydrochlorothiazide is a sulphonamide-derived medicinal product).

 Liver insufficiency or liver function impairment.

 Anuria, severe renal insufficiency (creatinine clearance < 30 ml/min.).

Acute heart failure, cardiogenic shock or episodes of heart failure decompensation requiring intravenous inotropic therapy.

 Sick sinus syndrome, including sino-atrial block.

Second and third-degree atrioventricular block (without a pacemaker).

Bradycardia (heart rate < 60 bpm prior to starting therapy).

Hypotension (systolic blood pressure < 90 mmHg).

Severe peripheral circulatory disturbances.

 History of bronchospasm and bronchial asthma.

Untreated phaeochromocytoma.

Metabolic acidosis.

Refractory hypokalaemia, hypercalcaemia, hyponatraemia and symptomatic hyperuricaemia

OTHER INFORMATION: Please refer to the Instruction sheet included in the package

MANUFACTURED BY:  AGIMEXPHARM PHARMACEUTICAL JOINT STOCK COMPANY

DISTRIBUTOR: GLOBAL PHARMACEUTICAL JOINT STOCK COMPANY

 

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