Concor

Concor

bisoprolol

Manufacturer:

PT. Merck Tbk
Concise Prescribing Info
Contents
Bisoprolol fumarate
Indications/Uses
Stable chronic heart failure w/ reduced systolic left ventricular function in addition to ACE inhibitors, & diuretics & optionally cardiac glycosides. 5 mg & 10 mg: HTN & CHD (angina pectoris).
Dosage/Direction for Use
Individualized dosage. HTN or angina pectoris Adult 5 mg once daily. May be increased to 10 mg once daily. Max recommended dose: 20 mg once daily. Severe renal impairment (CrCl <20 mL/min) & severe liver function disorders Not >10 mg. Stable chronic heart failure 1.25 mg once daily for 1 wk; if well tolerated increase to 2.5 mg once daily for a further wk; if well tolerated increase to 3.75 mg once daily for a further wk; if well tolerated increase to 5 mg once daily for the 4 following wk; if well tolerated increase to 7.5 mg once daily for the 4 following wk; if well tolerated increase to 10 mg once daily for the maintenance therapy. Max recommended dose: 10 mg once daily.
Administration
May be taken with or without food: Take in the morning. Swallow whole w/ some liqd, do not chew.
Contraindications
Hypersensitivity. Acute heart failure or during episodes of heart failure decompensation requiring IV inotropic therapy, cardiogenic shock, 2nd or 3rd degree AV block, sick sinus syndrome, SA block, symptomatic bradycardia, symptomatic hypotension, severe bronchial asthma or severe peripheral arterial occlusive disease or Raynaud's syndrome, untreated phaeochromocytoma, metabolic acidosis.
Special Precautions
Cessation of therapy must not be done abruptly. Regular monitoring during initiation & cessation of treatment. Patients w/ HTN or angina pectoris & accompanying heart failure. IDDM (type 1), restrictive cardiomyopathy, congenital heart disease, haemodynamically significant organic valvular disease, MI w/in 3 mth; bronchospasm (bronchial asthma, obstructive airways diseases), DM w/ large fluctuations in blood glucose values; symptoms of hypoglycaemia can be masked; strict fasting; ongoing desensitisation therapy. May increase both the sensitivity towards allergens and the severity of anaphylactic reactions. 1st degree AV block. Prinzmetal's angina. Peripheral arterial occlusive disease. General anaesth. Patients w/ or w/ a history of psoriasis. Phaeochromocytoma. May mask symptoms of thyreotoxicosis. May impair ability to drive a vehicle or to operate a machinery. Severe renal or hepatic impairment. Not to be used during pregnancy unless clearly necessary. Not recommended during breastfeeding. Childn.
Adverse Reactions
Bradycardia (in patients w/ chronic heart failure). Worsening of heart failure, asthenia (in patients w/ chronic heart failure); dizziness, headache; GI complaints eg, nausea, vomiting, diarrhoea, constipation; feeling of coldness or numbness in the extremities, hypotension; fatigue.
Drug Interactions
Effect on AV conduction time may be potentiated & -ve inotropic effect increased w/ class-I antiarrhythmic drugs (eg, quinidine, disopyramide; lidocaine, phenytoin; flecainide, propafenone). IV administration of verapamil in patients on β-blocker may lead to profound hypotension & AV block. May increase risk of rebound HTN in abrupt w/drawal of centrally acting BP-lowering medicines (eg, clonidine, methyldopa, moxonodine, rilmenidine) particularly if prior to β-blocker discontinuation. Increased risk of hypotension, & further deterioration of the ventricular pump function in patients w/ heart failure w/ concomitant use of Ca antagonists of the dihydropyridine type (eg, nifedipine, felodipine, amlodipine). Effect on AV conduction time may be potentiated w/ class III antiarrhythmic medicines (eg, amiodarone). Topical β-blockers (eg, eye drops for glaucoma treatment) may add to the systemic effects of Concor. Concomitant use of parasympathomimetic drugs may increase AV conduction time & the risk of bradycardia. Intensification of blood sugar lowering effect w/ insulin & oral antidiabetic drugs. Attenuation of the reflex tachycardia & increased risk of hypotension w/ anaesth agents. Reduction of heart rate, increase of AV conduction time w/ digitalis glycosides. NSAIDs may reduce the hypotensive effect of bisoprolol. May reduce the effect of both bisoprolol & β sympathomimetics (eg, isoprenaline, dobutamine). Combination w/ noradrenaline, adrenaline may unmask the α-adrenoceptor-mediated vasoconstrictor effect. Increased risk of hypotension w/ antihypertensive agents as well as other drugs w/ BP lowering potential (eg, TCAs, barbiturates, phenothiazines). Increased risk of bradycardia w/ mefloquine. Enhanced hypotensive effect of β-blockers but also risk of hypertensive crisis w/ MAOIs (except MAO-B inhibitors).
MIMS Class
Beta-Blockers
ATC Classification
C07AB07 - bisoprolol ; Belongs to the class of selective beta-blocking agents. Used in the treatment of cardiovascular diseases.
Presentation/Packing
Form
Concor FC tab 1.25 mg
Packing/Price
5 × 10's (Rp180,590/boks)
Form
Concor FC tab 10 mg
Packing/Price
3 × 10's (Rp335,948/boks)
Form
Concor FC tab 2.5 mg
Packing/Price
10 × 10's (Rp656,495/boks)
Form
Concor FC tab 5 mg
Packing/Price
10 × 10's (Rp950,648/boks)
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