Flecainide 50 mg Tablets
Flecainide 100 mg Tablets
Each tablet contains 50 mg flecainide acetate.
For the full list of excipients, see section 6.1.
Each tablet contains 100 mg flecainide acetate.
For the full list of excipients, see section 6.1.
White, normal convex 6.5 mm tablets, debossed “FC” over “50” on one side and “G” on the other.
Uncoated white, convex 8.5mm long tablets, with scoreline, debossed “FC” over “100” on one side and “G” on the other.
The scoreline is only to facilitate breaking for ease of swallowing and not to divide into equal doses.
It is recommended that treatment with Flecainide should be initiated in hospitals.
Flecainide are indicated for:
a) Symptomatic life threatening or disabling sustained ventricular tachycardia.
b) Premature ventricular contractions and/or non-sustained ventricular tachycardia which are causing disabling symptoms, where these are resistant to other therapy or when other treatment has not been tolerated.
c) AV nodal reciprocating tachycardia when patients have been unresponsive to beta-blockers or calcium channel blockers and in the absence of left ventricular dysfunction (see section 4.3).
d) Wolff-Parkinson White Syndrome and similar conditions with accessory pathways in the absence of left ventricular dysfunction (see section 4.3).
e) Paroxysmal atrial fibrillation and atrial flutter when treatment need has been established and in the absence of left ventricular dysfunction (see section 4.3).
Flecainide can be used for the maintenance of normal rhythm following conversion by other means.
Initiation of therapy should take place in the hospital environment with ECG monitoring.
Adults: The recommended starting dose is 50mg twice daily and most patients will be controlled at this dose the dose may be increased to a maximum of 300 mg daily.
Adults only: The recommended dose is 100 mg twice daily initially with subsequent increments of 50 mg daily every 4 days to the level of optimal response of a maximum dose of 400 mg daily with subsequent reduction after 3-5 days to the lowest dose compatible with control. Further reductions may be possible during long-term treatment.
Paediatric population Flecainide is not recommended in children under 18, as there is insufficient evidence of its use in this age group.
Older people: The rate of flecainide elimination from plasma may be reduced in older people. This should be taken into consideration when making dose adjustments.
Plasma levels: Based on PVC suppression, it appears that plasma levels of 200-1000 ng/ml may be needed to obtain the maximum therapeutic effect.
Plasma levels above 700-1000 ng/ml are associated with increased likelihood of adverse experiences. Regular monitoring is advisable and particularly if patients suffer from renal or hepatic dysfunction or are on other medication.
Patients with renal impairment: In patients with significant renal impairment (creatinine clearance of 35 ml/min/1.73 m2. or less) the maximum initial dosage should be 100 mg daily (or 50 mg twice daily). When used in such patients, frequent plasma monitoring is strongly recommended.
Treatment with oral Flecainide should be under direct hospital or specialist supervision for patients with:
a) AV nodal reciprocating tachycardia: arrhythmias associated with WPW Syndrome and similar conditions with accessory pathways.
b) Paroxysmal atrial fibrillation in patients with disabling symptoms.
Treatment for patients with other indications should continue to be initiated in hospital.
Method of administration
For oral use
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
Flecainide is contraindicated in patients with left ventricular dysfunction or cardiac failure, regardless of the type of arrhythmia, and in patients with a history of myocardial infarction who have either asymptomatic ventricular ectopics or asymptomatic non-sustained ventricular tachycardia.
Flecainide is contraindicated in the presence of cardiogenic shock.
It is also contraindicated in patients with long standing atrial fibrillation in whom there has been no attempt to convert to sinus rhythm, and in patients with haemodynamically significant valvular heart disease.
Use in patients with asymptomatic or non-life threatening symptomatic arrhythmias.
Known Brugada syndrome.
Unless pacing rescue is available, flecainide should not be given to patients with sinus node dysfunction, atrial conduction defects, second degree or third degree atrio-ventricular block, bundle branch block or distal block.
Use in patients with significant electrolyte imbalance.
Flecainide is contraindicated in patients with known hypersensitivity to amide drugs.
Use with other Class 1 antiarrhythmics.
Treatment with oral flecainide should be under direct hospital or specialist supervision for patients with:
• AV nodal reciprocating tachycardia; arrhythmias associated with Wolff-Parkinson-White Syndrome and similar conditions with accessory pathways.
• Paroxysmal atrial fibrillation in patients with disabling symptoms.
Flecainide has been shown to increase mortality risk of post-myocardial infarction patients with asymptomatic ventricular arrhythmia.
Flecainide, like other antiarrhythmics, may cause proarrhythmic effects, i.e. it may cause the appearance of a more severe type of arrhythmia, increase the frequency of an existing arrhythmia or the severity of the symptoms (see section 4.8).
Flecainide should be avoided in patients with structural heart disease or abnormal left ventricular function (see section 4.8).
Flecainide should be used with caution in patients with acute onset of atrial fibrillation following cardiac surgery.
Treatment for patients with other indications should continue to be initiated in hospital.
Intravenous treatment with flecainide should be initiated in hospital.
Continuous ECG monitoring is recommended in all patients receiving bolus injection.
Flecainide prolongs the QT interval and widens the QRS complex by 12-20 %. The effect on the JT interval is insignificant.
A Brugada syndrome may be unmasked due to flecainide therapy. In the case of development of ECG changes during treatment with flecainide that may indicate Brugada syndrome, consideration to discontinue the treatment should be made.
Since flecainide elimination from the plasma can be markedly slower in patients with significant hepatic impairment, flecainide should not be used in such patients unless the potential benefits clearly outweigh the risks. Plasma level monitoring is strongly recommended in these circumstances.
This product should be used with caution in patients with severe hepatic disease.
Flecainide should be used with caution in patients with impaired renal function (creatinine clearance ≤ 35 ml/min/1.73 m2) and therapeutic drug monitoring is recommended.
The rate of flecainide elimination from plasma may be reduced in the older people. This should be taken into consideration when making dose adjustments.
Electrolyte disturbances (e.g. hypo- and hyperkalaemia) should be corrected before using Flecainide, and should be checked during therapy particularly if diuretics are being administered (see section 4.5).
Severe bradycardia or pronounced hypotension should be corrected before using flecainide.
Flecainide is known to increase endocardial pacing thresholds – i.e. to decrease endocardial pacing sensitivity. This effect is reversible and is more marked on the acute pacing threshold than on the chronic. Flecainide should thus be used with caution in all patients with permanent pacemakers or temporary pacing electrodes, and should not be administered to patients with existing poor thresholds or non-programmable pacemakers unless suitable pacing rescue is available.
Generally, a doubling of either pulse width or voltage is sufficient to regain capture, but it may be difficult to obtain ventricular thresholds less than 1 Volt at initial implantation in the presence of Flecainide.
The minor negative inotropic effect of flecainide may assume importance in patients predisposed to cardiac failure. Difficulty has been experienced in defibrillating some patients. Most of the cases reported had pre-existing heart disease with cardiac enlargement, a history of myocardial infarction, arterio-sclerotic heart disease and cardiac failure.
Flecainide was included in the National Heart Lung and Blood Institute's Cardiac Arrhythmia Suppression Trial (CAST), a long-term, multi-centre, randomised, double-blind study in patients with asymptomatic non-life-threatening arrhythmias who had had a myocardial infarction more than six days, but less than two years, previously. An excessive mortality or non-fatal cardiac arrest rate was seen in patients treated with flecainide compared with that seen in a carefully matched placebo-treated group. This rate was 16/316 (5.1 %) for flecainide and 7/309 (2.3 %) for its matched placebo. The average duration of treatment with flecainide in this study was 10 months. It was noted that the increased risk from sudden cardiac death occurred in patients with a history of multiple previous myocardial infarction, usually with poor ventricular function.
Flecainide is not recommended in children under 18 years of age, as there is insufficient evidence of its use in this age group.
Dairy products (milk, infant formula and possibly yoghurt) may reduce the absorption of flecainide in children and infants. Flecainide is not approved for use in children below the age of 18 years, however flecainide toxicity has been reported during treatment with flecainide in children who reduced their intake of milk, and in infants who were switched from milk formula to dextrose feedings.
Flecainide as a narrow therapeutic index drug requires caution and close monitoring when switching a patient to a different formulation.
Flecainide is a class I antiarrhythmic and interactions are possible with other antiarrhythmic drugs where additive effects may occur or where drugs interfere with the metabolism of flecainide. The following known categories of drugs may interact with flecainide:
Cardiac glycosides: Flecainide can cause the plasma digoxin level to rise by about 15 %, which is unlikely to be of clinical significance for patients with plasma levels in the therapeutic range. It is recommended that the digoxin plasma level in digitalised patients should be measured not less than six hours after any digoxin dose, before or after administration of flecainide.
Class I antiarrhythmics: Flecainide should not be administered concomitantly with other class I antiarrythmics.
Class II antiarrhythmics: The possibility of additive negative inotropic effects of Class II antiarrhythmics, i.e. beta-blockers with flecainide should be recognised.
Class III antiarrhythmics: If flecainide is given in the presence of amiodarone the usual flecainide dosage should be reduced by 50 % and the patient monitored closely for adverse effects. Plasma level monitoring is strongly recommended in these circumstances.
Class IV antiarrhythmics: The use of flecainide with calcium channel blockers, e.g. verapamil, should be considered with caution.
Life-threatening or even lethal adverse events due to interactions causing increased plasma concentrations may occur (see section 4.9). Flecainide is metabolized by CYP2D6 to a large extent, and concurrent use of drugs inhibiting (e.g. antidepressants, neuroleptics, propranolol, ritonavir, some antihistamines) or inducing (e.g. phenytoin, phenobarbital, carbamazepine) this iso-enzyme can increase or decrease plasma concentrations of flecainide respectively.
An increase of plasma levels may also result from renal impairment due to a reduced clearance of flecainide (see section 4.4).
Hypokalaemia but also hyperkalaemia or other electrolyte disturbances should be corrected before administration of flecainide. Hypokalaemia may result from the concomitant use of diuretics, corticosteroids or laxatives.
Antidepressants: Fluoxetine, paroxetine and other antidepressants increases plasma flecainide concentration; increased risk of arrhythmias with tricyclics. Manufacturer of reboxetine advises caution.
Antiepileptics: Limited data in patients receiving known enzyme inducers (phenytoin, phenobarbital, carbamazepine) indicate only a 30 % increase in the rate of flecainide elimination.
Antipsychotics: Clozapine – increased risk of arrhythmias.
Antihistamines:Increased risk of ventricular arrhythmias with mizolastine and terfenadine (avoid concomitant use).
Antimalarials: Quinine increases plasma concentrations of flecainide.
Antivirals: Plasma concentrations are increased by ritonavir, lopinavir and indinavir (increased risk of ventricular arrhythmias) (avoid concomitant use).
Antifungals: Terbinafine may increase plasma concentrations of flecainide resulting from its inhibition of CYP2D6 activity.
Diuretics: Class effect due to hypokalaemia giving rise to cardiac toxicity.
H2 antihistamines (for the treatment of gastric ulcers): The H2-receptor antagonist cimetidine inhibits the metabolism of flecainide. In healthy subjects receiving cimetidine (1 g daily) for 1 week, the AUC of flecainide increased by about 30 % and the half-life increased by about 10 %.
Anti-smoking aids: Co-administration of bupropion with drugs that are metabolised by CYP2D6 isoenzyme including flecainide, should be approached with caution and should be initiated at the lower end of the dose range of the concomitant medication. If bupropion is added to the treatment regimen of a patient already receiving flecainide, the need to decrease the dose of the original medication should be considered.
Anticoagulants: The treatment with flecainide is compatible with the use of oral anticoagulants.
There is no evidence as to drug safety in human pregnancy. Data have shown that flecainide crosses the placenta to the foetus in patients taking flecainide during pregnancy. Flecainide should only be used in pregnancy if the benefit outweighs the risks.
Flecainide is excreted in human milk. Plasma concentrations obtained in a nursing infant are 5-10 times lower than therapeutic drug concentrations (see section 5.2). Although the risk of adverse effects to the nursing infant is very small, flecainide should only be used during lactation if the benefit outweighs the risks.
The ability to drive, operate machinery or undertake any other hazardous activity may be affected by adverse reactions such as dizziness and visual disturbances, if present.
Adverse events are listed below by system organ class and frequency. Frequencies are defined as: very common (≥1/l0), common (≥1/100 to <1/10), uncommon (≥1/1,000 to <1/100), rare (≥ 1/10,000 to <1/1,000) and very rare (<1/10,000), not known (cannot be estimated from the available data).
Blood and lymphatic system disorders:
Uncommon: red blood cell count decreased, white blood cell count decreased and platelet count decreased
Immune system disorders:
Very rare: antinuclear antibody increased with and without systemic inflammation
Rare: hallucination, depression, confusional state, anxiety, amnesia, insomnia
Nervous system disorders:
Very common: giddiness, dizziness and light headedness, which is usually transient
Rare: paraesthesia, ataxia, hypoaesthesia, hyperhidrosis, syncope, tremor, flushing, somnolence, headache, neuropathy peripheral, convulsion, dyskinesia
Very common: visual impairment, such as diplopia and vision blurred
Very rare: corneal deposits
Ear and labyrinth disorders:
Rare: tinnitus, vertigo
Common: proarrhythmia (most likely in patients with structural heart disease and/or significant left ventricular impairment).
Uncommon: patients with atrial flutter can develop a 1:1 AV conduction with increased heart rate.
Not known: dose-related increases in PR and QRS intervals may occur (see section 4.4). Altered pacing threshold (see section 4.4), atrioventricular block-second-degree and atrioventricular block third degree, cardiac arrest, bradycardia, cardiac failure/ cardiac failure congestive, chest pain, hypotension, myocardial infarction, palpitations, sinus arrest, and tachycardia (AT or VT) or ventricular fibrillation. Demasking of a pre-existing Brugada syndrome.
Respiratory, thoracic and mediastinal disorders:
Not known: pulmonary fibrosis, interstitial lung disease
Uncommon: nausea, vomiting, abdominal pain, constipation, decreased appetite, diarrhoea, dyspepsia, flatulence
Rare: hepatic enzymes increased with and without jaundice
Not known: hepatic dysfunction, cholestasis and hepatic failure
Skin and and subcutaneous tissue disorders:
Uncommon: dermatitis allergic, including rash, alopecia.
Rare: serious urticaria
Very rare: photosensitivity reaction
General disorders and administration site conditions:
Common: asthenia, fatigue, pyrexia, oedema
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via HPRA Pharmacovigilance, Earlsfort Terrace, IRL - Dublin 2; Tel: +353 1 6764971; Fax: +353 1 6762517. Website: www.hpra.ie; E-mail: email@example.com.
Overdosage with flecainide is a potentially life-threatening medical emergency. Increased drug susceptibility and plasma levels exceeding therapeutic levels may also result from drug interaction (see section 4.5). No specific antidote is known. There is no known way to rapidly remove flecainide from the system, but forced acid diuresis may theoretically be helpful. Neither dialysis nor haemoperfusion is effective and injections of anticholinergics is not recommended.
Treatment should be supportive and may include removal of unabsorbed drug from the GI tract. Further measures may include inotropic agents, intravenous calcium or cardiac stimulants such as dopamine, dobutamine or isoproterenol as well as mechanical ventilation and circulatory assistance (e.g. balloon pumping), mechanically assisting respiration, or temporarily inserting a transvenous pacemaker in the event of conduction block should be considered. Assuming a plasma half-life of approximately 20 hours, these supportive treatments may need to be continued for an extended period of time. Forced diuresis with acidification of the urine theoretically promotes drug excretion.
Pharmacotherapeutic group: Antiarrhythmics, class Ic, ATC code: C01BC04
Flecainide is a potent sodium channel blocking agent. Flecainide slows conduction through the heart having his greatest effect on His Bundle conduction. It also acts selectively to increase anterograde and particularly retrograde accessory pathway refractoriness. Its actions may be reflected in the ECG by prolongation of the PR interval and widening of QRS complex. The effect on the JT interval is insignificant.
Oral administration of flecainide results in extensive absorption, with bioavailability approaching 90 to 95 %. Flecainide does not appear to undergo significant hepatic first-pass metabolism. In patients, 200 to 500 mg flecainide daily produced plasma concentrations within the therapeutic range of 200 to 1000 µg/L. Protein binding of flecainide is within the range 32 to 58 %.
Recovery of unchanged flecainide in urine of healthy subjects was approximately 42 % of a 200 mg oral dose, whilst the two major metabolites (meta-O-dealkylated and dealkylated lactam metabolites) accounted for a further 14 % each. The elimination half-life was 12 to 27 hours. The volume of distribution is 8.7 l/kg.
In New Zealand white rabbits, high doses of flecainide produced some embryotoxic effects (increased resorption) and teratogenic effects (increased incidence of clubbed paws and skeletal abnormalities in sternebrae and vertebrae). Based on mg/kg body weight a safety margin of 8.7 for embryotoxic effects and 10.5 for teratogenic effects was calculated. These effects were not seen in Dutch belted rabbits or rats. The relevance of these findings to humans has not been established. Prolongation of gestation was seen in rats under a dose of 50mg/kg. No effects on fertility were observed
This medicinal product does not require any special storage conditions.
HDPE bottles with polypropylene child resistant caps and pressure seal wad.
Polypropylene tablet containers with polyethylene caps (with optional polyethylene ullage filler).
Polyvinyldene chloride coated polyvinylchloride/aluminium foil blisters.
Flecainide Tablets are available in the following pack sizes:
50 mg: 20, 30, 50, 60 and 100 tablets.
100 mg: 20, 30, 40, 50, 60 and 100 tablets.
Not all pack sizes may be marketed.
No special requirements.
McDermott Laboratories Ltd T/A Gerard Laboratories
35 – 36 Baldoyle Industrial Estate
Date of first authorisation: 13 June 2006
Date of latest renewal: 28 February 2010