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ATACAND PLUS TABLET [SIN11383P]
Active ingredients: ATACAND PLUS TABLET
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Product Info
ATACAND PLUS TABLET
[SIN11383P]
Product information
Active Ingredient and Strength | CANDESARTAN CILEXETIL - 16 MG |
Dosage Form | TABLET |
Manufacturer and Country | ASTRAZENECA AB - SWEDEN |
Registration Number | SIN11383P |
Licence Holder | ZUELLIG PHARMA PTE. LTD. |
Forensic Classification | PRESCRIPTION ONLY MEDICINES |
Anatomical Therapeutic Chemical (ATC) code | C09DA06 |
4.1 Therapeutic indications
Hypertension, where monotherapy with candesartan cilexetil or hydrochlorothiazide is not sufficient.
4.2 Posology and method of administration
Dosage in Hypertension
The recommended dose of Atacand Plus is 1 tablet once daily.
The dose of candesartan cilexetil should be titrated before switching to Atacand Plus.
Most of the antihypertensive effect is usually attained within 4 weeks of initiation of treatment.
When clinically appropriate a direct change from monotherapy to Atacand Plus may be considered. Dose titration of candesartan cilexetil is recommended when switching from hydrochlorothiazide monotherapy.
Administration
Atacand Plus should be taken once daily with or without food.
Use in the elderly
No dosage adjustment is necessary in elderly patients.
Use in patients with intravascular volume depletion
Dose titration of candesartan cilexetil is recommended in patients at risk for hypotension, such as patients with possible volume depletion (an initial dose of candesartan cilexetil of 4 mg may be considered in these patients).
Use in impaired renal function
In patients with mild to moderate renal impairment (ie, creatinine clearance between 30–80 ml/min/1.73 m2 BSA), a dose titration is recommended.
Atacand Plus should not be used in patients with severe renal impairment (creatinine clearance < 30 ml/min/1.73 m2 BSA).
Use in impaired hepatic function
Patients with hepatic impairment: Dose titration is recommended in patients with mild to moderate chronic liver disease.
Atacand Plus should not be used in patients with severe hepatic impairment and/or cholestasis.
Use in children
The safety and efficacy of Atacand Plus have not been established in children.
4.3 Contraindications
Hypersensitivity to the active substances or to any of the excipients or to sulfonamide derived drugs (hydrochlorothiazide is a sulfonamide derived drug) or to any of the excipients.
Pregnancy and lactation (see section Fertility, pregnancy and lactation – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
Severe renal impairment (creatinine clearance < 30 ml/min/1.73 m2 BSA).
Severe hepatic impairment and/or cholestasis.
Refractory hypokalaemia and hypercalcaemia.
Gout.
The concomitant use of Atacand Plus with aliskiren-containing products is contraindicated in patients with diabetes mellitus or renal impairment (GFR < 60 ml/min/1.73 m2) (see section Interaction with other medicinal products and other form of interaction – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
