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Ivacard 7.5 mg Tablet contains ivabradine, a prescription medicine that lowers the heart rate. It is used in appropriately selected patients with chronic stable angina and chronic heart failure. By slowing the heart rate, it reduces the heart's workload and oxygen requirement, allowing the heart to function more efficiently.
Ivacard 7.5 is generally taken twice daily with meals, preferably at consistent times each day. Do not stop the medicine or change the dose without consulting your doctor, even if you feel better.
Ivabradine acts specifically on the sinoatrial (SA) node, the heart's natural pacemaker. It selectively inhibits the If (“funny”) current, an electrical current responsible for controlling the spontaneous activity of pacemaker cells.
By slowing the generation of electrical impulses in the sinoatrial node, Ivacard 7.5 reduces the heart rate. This gives the heart more time to fill with blood between beats and reduces its oxygen requirement and workload. Unlike some other medicines that slow the heart, ivabradine does not directly reduce the strength of heart-muscle contraction.
Ivacard 7.5 should not be used in patients with:
The safety and effectiveness of ivabradine in children and adolescents have not been established. It should therefore not be used in this population unless specifically prescribed by an appropriate specialist.
Patients with severe renal impairment require medical supervision. No routine dose adjustment is generally required when creatinine clearance is above 15 mL/min, while limited data are available for patients with creatinine clearance below 15 mL/min.
For patients aged 75 years or older, treatment may be initiated at a lower dose, such as 2.5 mg twice daily, with subsequent adjustment according to response and tolerability.
The usual starting dose is 5 mg twice daily with meals. Depending on the therapeutic response, the dose may be increased to 7.5 mg twice daily after approximately 3–4 weeks.
If the resting heart rate persistently falls below 50 beats/minute, or symptoms of bradycardia such as dizziness, weakness, or fatigue occur, the dose may need to be reduced to 2.5 mg twice daily. Treatment should be discontinued if the heart rate remains below 50 beats/minute or symptoms of bradycardia continue.
The usual starting dose is 5 mg twice daily with meals. The dose is adjusted according to resting heart rate and tolerability.
Pregnancy:
Ivacard 7.5 should not be used during pregnancy. Women who are pregnant, planning to become pregnant, or capable of becoming pregnant should consult their doctor regarding appropriate treatment and contraception.
Breastfeeding:
Breastfeeding is not recommended during treatment with ivabradine because the medicine may pass into breast milk. Consult your doctor about suitable alternatives.
Strong CYP3A4 inhibitors:
Medicines such as certain azole antifungals, macrolide antibiotics, and HIV protease inhibitors can significantly increase ivabradine concentrations and may cause excessive slowing of the heart rate. These combinations are generally contraindicated.
Heart-rate-lowering medicines:
Combining ivabradine with other medicines that slow the heart rate can increase the risk of bradycardia. Particular caution is required with medicines such as beta-blockers and certain calcium-channel blockers.
Verapamil and diltiazem:
These medicines may increase ivabradine exposure and further reduce the heart rate; concomitant use is generally not recommended.
QT-prolonging medicines:
Medicines that prolong the QT interval may increase the risk of abnormal heart rhythms when combined with ivabradine, particularly because ivabradine lowers the heart rate. Appropriate medical monitoring is required if such combinations cannot be avoided.
CYP3A4 inducers:
Medicines such as rifampicin, phenytoin, barbiturates, and St John's wort may reduce ivabradine concentrations and decrease its effectiveness.
Grapefruit and grapefruit juice should be avoided, as they can increase ivabradine exposure and potentially increase the risk of excessive slowing of the heart rate.
Ivabradine begins to exert its heart-rate-lowering effect relatively soon after administration, with effects generally extending over the dosing interval. Individual response varies, so the dose and treatment schedule should be determined by the prescribing physician.
⚠️Disclaimer:
At ePharma, we’re committed to providing accurate and accessible health information. However, all content is intended for informational purposes only and should not replace medical advice from a qualified physician. Please consult your healthcare provider for personalized guidance. We aim to support, not substitute, the doctor-patient relationship.