Buy Tambocor
Tambocor

1.73
A potent heart rhythm regulator used to treat and prevent serious irregular heartbeats.


Ingredient
Availability
In Stock
Delivery
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Active Ingredient(s)
Flecainide
Primary Category
Heart & Blood Pressure, Arrhythmia
Therapeutic Class
Cardiac therapy, Antiarrhythmics, class IC
Pharmacological Class
Sodium channel blocker
Indications
Atrial fibrillation, Supraventricular tachycardia, Ventricular arrhythmias
Contraindications
Heart failure, History of myocardial infarction, Brugada syndrome
Minor Side Effects
Dizziness, Blurred vision, Nausea
Moderate Side Effects
Breathlessness, Fatigue, Headache
Serious Side Effects
Pro-arrhythmic effects (new arrhythmias), Cardiac arrest, Hepatotoxicity
Dosage Forms
Tablet, Injection
Administration Route
Oral
Mechanism of Action
Flecainide slows down the electrical signals in the heart to help maintain a normal, steady rhythm and prevent irregular heartbeats.
Prescription Status
Rx
Manufacturer
Meda Pharmaceuticals
Patient Summary
A potent heart rhythm regulator used to treat and prevent serious irregular heartbeats.
Onset Time
1-3 hours
Duration
12-27 hours
Storage Instructions
Store at room temperature
Drug Interactions
Digoxin, Amiodarone, Beta-blockers, Ritonavir
Age Restrictions
Adults primarily; specialist use in children
Pregnancy Use
Avoid unless benefits outweigh risks
Alternative Drugs
Propafenone, Sotalol

What is Tambocor?

Tambocor is a brand-name medication that contains the active ingredient flecainide. Flecainide belongs to the class IC anti-arrhythmic drugs and is used to treat certain abnormal heart rhythms. In Hong Kong, Tambocor is available only by prescription and is supplied as an oral pill in two strengths: 50 mg and 100 mg. The medication is regulated by the Hong Kong Department of Health, which follows standards similar to those of the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA).

How Tambocor Works in the Body

Flecainide works by blocking fast-acting sodium channels in cardiac cells. By reducing the influx of sodium during the early phase of the cardiac electrical impulse, the drug:

  • Slows the conduction of electrical signals through the heart muscle, especially in the atria, ventricles, and the His-Purkinje system.
  • Prolongs the refractory period, making it harder for an abnormal rhythm to re-initiate.

These actions help restore a normal rhythm in patients with supraventricular tachycardia (SVT) or certain ventricular arrhythmias. The drug is rapidly absorbed after oral administration, reaching peak blood levels within 1-3 hours. It is metabolized mainly by the liver and excreted unchanged in the urine.

Conditions Treated by Tambocor

Tambocor is approved for the following indications, consistent with regulatory labeling in Hong Kong and internationally:

  • Paroxysmal supraventricular tachycardia (PSVT) - episodes of rapid heartbeats that start and stop abruptly.
  • Ventricular tachycardia (VT) - sustained rapid rhythms originating from the ventricles, when other therapies are unsuitable.
  • Atrial fibrillation (AF) or atrial flutter - in patients without significant structural heart disease, where rhythm control is preferred.

These uses are based on clinical trials that demonstrated flecainide’s ability to convert or maintain sinus rhythm and to suppress recurrent ventricular episodes.

Patient Suitability and Contra­indications

Who Should Use Tambocor?

  • Adults with documented SVT, VT, or AF who do not have structural heart disease (e.g., prior myocardial infarction, cardiomyopathy) and who have normal left-ventricular function.
  • Patients who have been evaluated with an electrocardiogram (ECG) and possibly an electrophysiology study confirming that flecainide is appropriate.

Absolute Contra­indications

  • Known hypersensitivity to flecainide or any tablet excipients.
  • History of myocardial infarction or clinically significant coronary artery disease.
  • Left-ventricular ejection fraction < 40 % (moderate to severe heart failure).
  • Second- or third-degree atrioventricular (AV) block without a functioning pacemaker.
  • Concomitant use of Class I anti-arrhythmics (e.g., quinidine, procainamide) that may increase pro-arrhythmic risk.
  • Pregnancy - flecainide is classified as a Category C drug; it should be avoided unless the benefit clearly outweighs the risk.
  • Severe hepatic impairment (Child-Pugh C) or renal failure requiring dialysis.

Relative Contra­indications

  • Elderly patients - may require lower initial doses and careful ECG monitoring.
  • Mild to moderate hepatic or renal dysfunction - dose adjustments may be needed.
  • Concomitant beta-blockers or calcium-channel blockers - may increase bradycardia risk; monitoring is advised.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Dizziness or light-headedness
  • Visual disturbances (e.g., blurred vision, photophobia)
  • Nausea or mild gastrointestinal upset
  • Fatigue or generalized weakness
  • Palpitations (often due to premature beats)

These reactions are usually transient and may improve with dose titration.

Serious Adverse Events

  • Pro-arrhythmia - new or worsening arrhythmias, especially in patients with underlying heart disease.
  • Heart failure exacerbation - marked reduction in cardiac output.
  • Sudden cardiac death - rare but reported in patients with structural heart disease.
  • Conduction abnormalities - severe AV block or severe bradycardia, requiring immediate medical attention.

A black-box warning accompanies flecainide labeling to highlight the risk of life-threatening arrhythmias in unsuitable patients.

Drug Interactions

  • Major Interactions
  • CYP2D6 inhibitors (e.g., quinidine, propafenone, bupropion) can raise flecainide plasma levels → increased toxicity.
  • Other Class I anti-arrhythmics (e.g., propafenone) - additive sodium-channel blockade.
  • Beta-blockers (e.g., metoprolol) - may cause excessive slowing of heart rate.
  • Moderate Interactions
  • Digoxin - increased risk of AV block; monitor levels and ECG.
  • Calcium-channel blockers (e.g., diltiazem) - may enhance bradycardic effect.

Mechanism: many interactions involve inhibition of hepatic metabolism (CYP2D6) or additive electrophysiological effects on cardiac conduction.

Food and Lifestyle Interactions

  • Alcohol - can potentiate dizziness and enhance arrhythmic risk; moderate consumption is advisable.
  • Grapefruit juice - may modestly inhibit CYP2D6; patients should limit intake.
  • Driving or operating machinery - avoid if experiencing dizziness, visual changes, or significant bradycardia.

If you are taking other prescription medicines, over-the-counter drugs, or herbal supplements, inform your healthcare provider before starting Tambocor.

How to Take Tambocor

Standard Dosing (Adults)

  • Initiation: 50 mg taken orally twice daily (approximately 12 hours apart).
  • Titration: Based on ECG response and symptom control, the dose may be increased to 100 mg twice daily.
  • Maximum Recommended Dose: 300 mg per day (typically as 150 mg twice daily) in select cases, but only under specialist supervision.

Special Populations

  • Renal impairment (CrCl < 50 mL/min): Consider a 25 % dose reduction; monitor plasma levels if available.
  • Mild hepatic dysfunction (Child-Pugh A-B): Start with 50 mg once daily, then adjust cautiously.
  • Elderly (> 75 years): Initiate at 50 mg once daily; increase only if tolerated and clinically indicated.

Administration of the Pill

  • Swallow the tablet whole with a full glass of water.
  • Can be taken with or without food; however, taking it with food may reduce occasional stomach upset.

Missed Dose

  • If you remember the missed dose within 6 hours, take it promptly.
  • If it is closer to the time of the next scheduled dose, skip the missed dose and resume the regular schedule. Do not double the dose.

Overdose Management

  • Symptoms: Severe nausea, vomiting, dizziness, visual disturbances, or life-threatening arrhythmias.
  • Emergency Action: Seek immediate medical attention; treatment may include activated charcoal, cardiac monitoring, and intravenous sodium bicarbonate for ventricular arrhythmias.

Discontinuation

  • Abrupt cessation can precipitate rebound arrhythmias.
  • Gradual tapering (e.g., reducing dose by 25 % every 1-2 weeks) is recommended under physician guidance, especially after long-term use.

Monitoring and Follow-Up

  • Baseline ECG before initiating therapy to document QRS duration and identify conduction abnormalities.
  • Follow-up ECG 1-2 weeks after dose changes; then every 3-6 months for stable patients.
  • Plasma flecainide levels (therapeutic range ≈ 0.2-1.0 µg/mL) may be measured in complex cases or when toxicity is suspected.
  • Renal and hepatic function tests at baseline and periodically, especially in patients with known impairment.
  • Clinical assessment for signs of worsening heart failure, new palpitations, dizziness, or visual symptoms at each visit.

Storage and Handling

  • Store Tambocor tablets at room temperature (20-25 °C), protected from moisture and direct sunlight.
  • Keep the container tightly closed and out of reach of children.
  • Do not use the medication after the expiration date printed on the packaging.
  • Dispose of unused tablets in accordance with local pharmaceutical waste guidelines (e.g., return to a pharmacy or use a medication take-back program).

Medication-Specific Glossary

Na⁺ Channel Blocker
A drug that inhibits the rapid influx of sodium ions during cardiac depolarization, thereby slowing electrical conduction.
Pro-arrhythmia
The paradoxical worsening or new onset of cardiac arrhythmias caused by an anti-arrhythmic medication.
Therapeutic Window
The concentration range in which a drug is effective without causing unacceptable toxicity; for flecainide, this is a relatively narrow plasma level range.
QT Interval
The portion of the ECG that reflects total ventricular depolarization and repolarization; flecainide can modestly prolong this interval, necessitating ECG monitoring.

Medical Disclaimer

This article provides educational information about Tambocor and is not a substitute for professional medical advice. Treatment decisions, including use for unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Tambocor FAQ

Can I take Tambocor with other anti-arrhythmic drugs?

Combining flecainide with other Class I anti-arrhythmics (e.g., quinidine, propafenone) can increase the risk of serious conduction disturbances. Such combinations should only be used under strict specialist supervision with continuous ECG monitoring.

How long does it take for Tambocor to start working?

After oral ingestion, flecainide reaches peak blood concentrations within 1-3 hours. Patients often notice a reduction in arrhythmic episodes within the first few days, but full therapeutic effect may require several weeks of steady dosing.

Will taking Tambocor affect my blood pressure?

Flecainide primarily influences heart rhythm rather than blood pressure. However, in some individuals it may cause mild hypotension, especially when combined with beta-blockers or calcium-channel blockers.

Is it safe to travel internationally with Tambocor?

Yes, but keep the medication in its original labeled container, carry a copy of the prescription, and be aware of Hong Kong’s customs rules for controlled medicines. Short-term travel does not usually require additional documentation.

What should I do if I experience visual disturbances while on Tambocor?

Visual symptoms such as blurred vision or photophobia can be an early sign of flecainide toxicity. Contact your healthcare provider promptly; dose adjustment or further evaluation may be necessary.

Can I use Tambocor if I have mild liver disease?

Mild hepatic impairment (Child-Pugh A) generally permits standard dosing, but many clinicians start at a lower dose (e.g., 50 mg once daily) and monitor liver function tests and ECG closely.

Does grapefruit juice interact with Flecainide?

Grapefruit juice can modestly inhibit CYP2D6, the enzyme that metabolizes flecainide, potentially raising drug levels. It is advisable to limit grapefruit consumption while taking Tambocor.

Are there any over-the-counter supplements that should be avoided?

Certain herbal products like St. John’s Wort induce CYP enzymes and may lower flecainide concentrations, reducing efficacy. Always discuss any supplements with your pharmacist or physician.

How can I tell if my dose is too high?

Signs of excessive dosing include persistent dizziness, significant visual changes, severe fatigue, or new arrhythmic episodes. If any of these occur, seek medical advice promptly for possible dose reduction.

What is the difference between Tambocor and other anti-arrhythmics like amiodarone?

Tambocor (flecainide) is a Class IC sodium-channel blocker with a relatively short half-life and a narrow therapeutic window. Amiodarone is a Class III potassium-channel blocker with a very long half-life and a broader safety profile, but it carries distinct organ-specific toxicities (e.g., thyroid, pulmonary). Choice of agent depends on the specific arrhythmia, patient comorbidities, and physician expertise.

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