- Approval Id
- 9350ad652f6684c0
- Drug Name
- IVASWIFT FILM-COATED TABLET 7.5MG
- Product Name
- IVASWIFT FILM-COATED TABLET 7.5MG
- Approval Number
- SIN16201P
- Approval Date
- 2021-05-20
- Registrant
- GOLDPLUS UNIVERSAL PTE LTD
- Licence Holder
- GOLDPLUS UNIVERSAL PTE LTD
- Drug Type
- Therapeutic
- Forensic Classification
- PRESCRIPTION ONLY MEDICINES
- Dosage Form
- TABLET, FILM COATED
- Dosage
- <p><strong>DOSAGE & ADMINISTRATION:</strong><br>
<u><strong>Posology</strong></u><br>
For the different doses, film-coated tablets containing 5 mg and 7.5 mg ivabradine are available. Symptomatic treatment of chronic stable angina pectoris.</p>
<p>It is recommended that the decision to initiate or titrate treatment takes place with the availability of serial heart rate measurements, ECG or ambulatory 24-hour monitoring.</p>
<p>The starting dose of ivabradine should not exceed 5 mg twice daily in patients aged below 75 years. After three to four weeks of treatment, if the patient is still symptomatic, if the initial dose is well tolerated and if resting heart rate remains above 60 bpm, the dose may be increased to the next higher dose in patients receiving 2.5 mg twice daily or 5 mg twice daily. The maintenance dose should not exceed 7.5 mg twice daily.</p>
<p>If there is no improvement in symptoms of angina within 3 months after start of treatment, treatment of ivabradine should be discontinued.</p>
<p>In addition, discontinuation of treatment should be considered if there is only limited symptomatic response and when there is no clinically relevant reduction in resting heart rate within three months.</p>
<p>If, during treatment, heart rate decreases below 50 beats per minute (bpm) at rest or the patient experiences symptoms related to bradycardia such as dizziness, fatigue or hypotension, the dose must be titrated downward including the lowest dose of 2.5 mg twice daily (one half 5 mg tablet twice daily). After dose reduction, heart rate should be monitored. Treatment must be discontinued if heart rate remains below 50 bpm or symptoms of bradycardia persist despite dose reduction.</p>
<p>Treatment of chronic heart failure.<br>
The treatment has to be initiated only in patient with stable heart failure. It is recommended that the treating physician should be experienced in the management of chronic heart failure.</p>
<p>The usual recommended starting dose of ivabradine is 5 mg twice daily. After two weeks of treatment, the dose can be increased to 7.5 mg twice daily if resting heart rate is persistently above 60 bpm or decreased to 2.5 mg twice daily (one half 5 mg tablet twice daily) if resting heart rate is persistently below 50 bpm or in case of symptoms related to bradycardia such as dizziness, fatigue or hypotension. If heart rate is between 50 and 60 bpm, the dose of 5 mg twice daily should be maintained.</p>
<p>If during treatment, heart rate decreases persistently below 50 beats per minute (bpm) at rest or the patient experiences symptoms related to bradycardia, the dose must be titrated downward to the next lower dose in patients receiving 7.5 mg twice daily or 5 mg twice daily. If heart rate increases persistently above 60 beats per minute at rest, the dose can be up titrated to the next upper dose in patients receiving 2.5 mg twice daily or 5 mg twice daily.</p>
<p>Treatment must be discontinued if heart rate remains below 50 bpm or symptoms of bradycardia persist.</p>
<p><u>Special Population</u></p>
<p><em>Elderly</em><br>
In patients aged 75 years or more, a lower starting dose should be considered for these patients (2.5 mg twice daily i.e. one half 5 mg tablet twice daily) before up-titration if necessary.</p>
<p><em>Renal impairment</em><br>
No dose adjustment is required in patients with renal insufficiency and creatinine clearance above 15 ml/min.</p>
<p>No data are available in patients with creatinine clearance below 15 ml/min. Ivabradine should therefore be used with precaution in this population.</p>
<p><em>Hepatic impairment</em><br>
No dose adjustment is required in patients with mild hepatic impairment. Caution should be exercised when using ivabradine in patients with moderate hepatic impairment. Ivabradine is contra-indicated for use in patients with severe hepatic insufficiency, since it has not been studied in this population and a large increase in systemic exposure is anticipated.</p>
<p><em>Paediatric population</em><br>
The safety and efficacy of ivabradine in children aged below 18 years have not yet been established. No data are available.</p>
<p><u>Route of administration</u>: Oral Route.</p>
<p><u>Method of administration</u><br>
Tablets must be taken orally twice daily, i.e. once in the morning and once in the evening during meals.</p>
<p><strong>Effects on ability to drive and use machines</strong><br>
A specific study to assess the possible influence of ivabradine on driving performance has been performed in healthy volunteers where no alteration of the driving performance was evidenced. However, in post-marketing experience, cases of impaired driving ability due to visual symptoms have been reported. Ivabradine may cause transient luminous phenomena consisting mainly of phosphenes. The possible occurrence of such luminous phenomena should be taken into account when driving or using machines in situations where sudden variations in light intensity may occur, especially when driving at night. Ivabradine has no or negligible influence on the ability to use machines.</p>
- Route Of Administration
- ORAL
- Indication Info
- <p><strong>INDICATIONS:</strong><br>
<strong>Symptomatic treatment of chronic stable angina pectoris.</strong><br>
Ivabradine is indicated for the symptomatic treatment of chronic stable angina pectoris in coronary artery disease adults with normal sinus rhythm and heart rate ≥ 70 bpm. Ivabradine is indicated:</p>
<ul class="dash">
<li>in adults unable to tolerate or with a contra-indication to the use of beta-blockers</li>
<li>or in combination with beta-blockers in patients inadequately controlled with an optimal beta-blocker dose.</li>
</ul>
<p><strong>Treatment of chronic heart failure</strong><br>
Ivabradine is indicated in chronic heart failure NYHA II to IV class with systolic dysfunction, in patients in sinus rhythm and whose heart rate is ≥ 75 bpm, in combination with standard therapy including beta-blocker therapy or when beta-blocker therapy is contraindicated or not tolerated.</p>
- Contraindications
- <p><strong>CONTRAINDICATION:</strong></p>
<ul class="dash">
<li>Hypersensitivity to the active substance or to any of the excipients</li>
<li>Resting heart rate below 70 beats per minute prior to treatment</li>
<li>Cardiogenic shock</li>
<li>Acute myocardial infarction</li>
<li>Severe hypotension (< 90/50 mmHg)</li>
<li>Severe hepatic insufficiency</li>
<li>Sick sinus syndrome</li>
<li>Sino-atrial block</li>
<li>Unstable or acute heart failure</li>
<li>Pacemaker dependent (heart rate imposed exclusively by the pacemaker)</li>
<li>Unstable angina</li>
<li>AV-block of 3rd degree</li>
<li>Combination with strong cytochrome P450 3A4 inhibitors such as azole antifungals (ketoconazole, itraconazole), macrolide antibiotics (clarithromycin, erythromycin <em>per os</em>, josamycin, telithromycin), HIV protease inhibitors (nelfinavir, ritonavir) and nefazodone</li>
<li>Combination with verapamil or diltiazem which are moderate CYP3A4 inhibitors with heart rate reducing properties</li>
<li>Pregnancy, lactation and women of child bearing potential not using appropriate contraceptive measures</li>
</ul>
- Atc Code
- C01EB17
- Atc Item Name
- ivabradine
- Pharma Manufacturer Name
- GOLDPLUS UNIVERSAL PTE LTD
