Vertab Sr 240 Tablets
Out of date information, search anotherPRODUCT SUMMARY
1. NAME OF THE MEDICINAL PRODUCT Vertab SR 240 Tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Verapamil HCI 240.0 mg
Also contains microcrystalline cellulose and about 32 mg of sodium.
For a full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Modified-Release tablets
The score line is only to facilitate breaking for ease of swallowing and not to divide into equal doses.
4 CLINICAL PARTICULARS
4.1. Therapeutic Indications
Vertab SR 240 is indicated for the treatment of mild to moderate hypertension, and the treatment and prophylaxis of angina pectoris.
4.2 Posology and method of administration
Adults:
Hypertension: Most patients respond to 240 mg daily (one tablet) given as a single dose. If control is not achieved after a period of at least one week the dosage may be increased to a maximum of two Vertab SR 240 tablets daily (one in the morning and one in the evening at an interval of about twelve hours). A further reduction in blood pressure may be achieved by combining Vertab SR 240 with other anti-hypertensive agents, in particular diuretics.
Angina pectoris: One tablet of Vertab SR 240 twice daily. A small number of patients respond to a lower dose and where indicated, adjustment down to one tablet of Vertab SR 240 daily could be made.
Elderly patients: The adult dose is recommended unless liver or renal function is impaired (see Precautions).
The tablets should not be chewed.
Paediatric population
The safety and efficacy of verapamil prolonged release tablets in children and adolescents have not been established. No data are available.
4.3 Contraindications
Hypersensitivity to the active substance or to any of the excipients.
Cardiogenic shock; acute myocardial infarction complicated by bradycardia, marked hypotension, left ventricular failure; second or third degree atrioventricular (AV) block (except in patients with a functioning artificial pacemaker); sino-atrial block; sick sinus syndrome (except in patients with a functioning artificial pacemaker); uncompensated heart failure; bradycardia of less than 50 beats/minute; hypotension of less than 90 mm Hg systolic.
Patients with atrial flutter/fibrillation in the presence of an accessory pathway (e.g. WPW syndrome) may develop increased conduction across the anomalous pathway and ventricular tachycardia may be precipitated.
4.4 Special warnings and precautions for use
Since Verapamil is extensively metabolised in the liver, careful dose-titration is required in patients with liver disease. Although the pharmacokinetics of Verapamil in patients with renal impairment are not affected, caution should be exercised and careful patient monitoring is recommended. Verapamil is not removed during dialysis.
Verapamil may affect impulse conduction and should therefore be used with caution in patients with bradycardia or first degree AV block. Verapamil may affect left ventricular contractility; this effect is small and normally not important but cardiac failure may be precipitated or aggravated. In patients with incipient cardiac failure, therefore, Verapamil should be given only after such cardiac failure has been controlled with appropriate therapy, e.g. digitalis.
When treating hypertension with Verapamil, monitoring of the patient’s blood pressure at regular intervals is required.
Caution should be exercised in treatment with HMG CoA reductase inhibitors (e.g., simvastatin, atorvastatin or lovastatin) for patients taking Verapamil. These patients should be started at the lowest possible dose of Verapamil and titrated upwards. IfVerapamil treatment is to be added to patients already taking an HMG CoA reductase inhibitor (e.g., simvastatin, atorvastatin or lovastatin), refer to advice in the respective statin product information.
Use with caution in the presence of diseases in which neuromuscular transmission is affected (myasthenia gravis, Lambert-Eaton syndrome, advanced Duchenne muscular dystrophy).
4.5 Interaction with other medicinal products and other forms of interaction
In vitro metabolic studies indicate that Verapamil hydrochloride is metabolized by cytochrome P450 CYP3A4, CYP1A2, CYP2C8, CYP2C9 and CYP2C18. Verapamil has been shown to be an inhibitor of CYP3A4 enzymes and P-glycoprotein (P-gp). Clinically significant interactions have been reported with inhibitors of CYP3A4 causing elevation of plasma levels of Verapamil hydrochloride while inducers of CYP3A4 have caused a lowering of plasma levels of Verapamil hydrochloride, therefore, patients should be monitored for drug interactions.
The following are potential drug interactions associated with Verapamil:
Acetylsalicylic acid
Concomitant use of Verapamil with aspirin may increase the risk of bleeding Alcohol
Increase in blood alcohol has been reported.
Alpha blockers
Verapamil may increase the plasma concentrations of prazosin and terazosin which may have an additive hypotensive effect.
Antiarrhythmics
Verapamil may slightly decrease the plasma clearance offlecainide whereas flecainide has no effect on the Verapamil plasma clearance.
Verapamil may increase the plasma concentrations of quinidine. Pulmonary oedema may occur in patients with hypertrophic cardiomyopathy.
The combination of Verapamil and antiarrhythmic agents may lead to additive cardiovascular effects (e.g. AV block, bradycardia, hypotension, heart failure).
Anticonvulsants
Verapamil may increase the plasma concentrations of carbamazepine. This may produce side effects such as diplopia, headache, ataxia or dizziness. Verapamil may also increase the plasma concentrations of phenytoin.
Antidepressants
Verapamil may increase the plasma concentrations of imipramine.
Antidiabetics
Verapamil may increase the plasma concentrations of glibenclamide (glyburide).
Antihypertensives, diuretics, vasodilators Potentiation of the hypotensive effect.
Anti-infectives
Rifampicin may reduce the plasma concentrations of Verapamil which may produce a reduced blood pressure lowering effect. Erythromycin, clarithromycin and telithromycin may increase the plasma concentrations of Verapamil.
Antineoplastics
Verapamil may increase the plasma concentrations of doxorubicin.
Barbiturates
Phenobarbital may reduce the plasma concentrations of Verapamil.
Benzodiazepines and other anxiolytics
Verapamil may increase the plasma concentrations of buspirone and midazolam.
Beta blockers
Verapamil may increase the plasma concentrations of metoprolol and propranolol which may lead to additive cardiovascular effects (e.g. AV block, bradycardia, hypotension, heart failure).
Intravenous beta-blockers should not be given to patients under treatment with Verapamil.
Cardiac glycosides
Verapamil may increase the plasma concentrations of digitoxin and digoxin. Verapamil has been shown to increase the serum concentration of digoxin and caution should be exercised with regard to digitalis toxicity. The digitalis level should be determined and the glycoside dose reduced, if required.
Colchicine
Colchicine is a substrate for both CYP3A and the efflux transporter, P-glycoprotein (P-gp). Verapamil is known to inhibit CYP3A and P-gp. When Verapamil and colchicine are administered together, inhibition of P-gp and/or CYP3A by Verapamil may lead to increased exposure to colchicine. Combined use is not recommended.
H2 Receptor antagonists
Cimetidine may increase the plasma concentrations of Verapamil.
HIV antiviral agents
Due to the metabolic inhibitory potential of some of the HIV antiviral agents, such as ritonavir, plasma concentrations of Verapamil may increase. Caution should be used or dose of Verapamil may be decreased.
Immunosuppressants
Verapamil may increase the plasma concentrations of ciclosporin, everolimus, sirolimus and tacrolimus.
Inhaled anaesthetics
When used concomitantly, inhalation anaesthetics and calcium antagonists, such as Verapamil hydrochloride, should each be titrated carefully to avoid additive cardiovascular effects (e.g. AV block, bradycardia, hypotension, heart failure).
Lipid lowering agents
Verapamil may increase the plasma concentrations of atorvastatin, lovastatin and simvastatin.
Treatment with HMG CoA reductase inhibitors (e.g., simvastatin, atorvastatin or lovastatin) in a patient taking Verapamil should be started at the lowest possible dose and titrated upwards. If Verapamil treatment is to be added to patients already taking an HMG CoA reductase inhibitor (e.g., simvastatin, atorvastatin or lovastatin), consider a reduction in the statin dose and retitrate against serum cholesterol concentrations.
Atorvastatin may increase Verapamil levels. Although there is no direct in vivo clinical evidence, there is strong potential for Verapamil to significantly affect atorvastatin pharmacokinetics in a similar manner to simvastatin or lovastatin. Consider using caution when atorvastatin and Verapamil are concomitantly administered.
Fluvastatin, pravastatin and rosuvastatin are not metabolized by CYP3A4 and are less likely to interact with Verapamil.
Lithium
Serum levels of lithium may be reduced. However, there may be increased sensitivity to lithium causing enhanced neurotoxicity.
Neuromuscular blocking agents employed in anaesthesia
The effects may be potentiated.
Serotonin receptor agonists
Verapamil may increase the plasma concentrations of almotriptan. Theophylline
Verapamil may increase the plasma concentrations of theophylline.
Uricosurics
Sulfinpyrazone may reduce the plasma concentrations of Verapamil which may produce a reduced blood pressure lowering effect.
Other
St. John's Wort may reduce the plasma concentrations of Verapamil, whereas grapefruit juice may increase the plasma concentrations of Verapamil.
4.6 Pregnancy and lactation
Although animal studies have not shown any teratogenic effects, Verapamil should not be given during the first trimester of pregnancy unless, in the clinician’s judgement, it is essential for the welfare of the patient.
Verapamil hydrochloride is excreted in human breast milk. Limited human data from oral administration has shown that the infant relative dose of verapamil is low (0.1 -1% of the mother's oral dose) and that verapamil use may be compatible with breastfeeding. Due to the potential for serious adverse reactions in nursing infants, verapamil should only be used during lactation if it is essential for the welfare of the mother.
4.7 Effects on ability to drive and use machines
Depending on individual susceptibility, the patients’ ability to drive a vehicle, operate machinery or work under hazardous conditions may be impaired. This is particularly true in the initial stages of treatment, when changing over from another drug or when the dose is raised. Like many other common medicines, Verapamil has been shown to increase the blood levels of alcohol and slow its elimination. Therefore the effects of alcohol may be exaggerated.
4.8 Undesirable effects
Reactions from Postmarketing Surveillance or Phase IV Clinical Trials
The following adverse events reported with Verapamil are listed below by system organ class:
Immune system disorders: allergic reactions (e.g. erythema, pruritus, urticaria) are very rarely seen.
Nervous system disorders: headache, dizziness, paresthesia, tremor and extrapyramidal syndrome.
Ear and labyrinth disorders: vertigo and tinnitus.
Cardiac disorders/vascular disorders: bradycardic arrhythmias such as sinus bradycardia, sinus arrest with asystole, 2nd and 3rd degree AV block, bradyarrhythmia in atrial fibrillation, peripheral oedema, palpitations, tachycardia, development or aggravation of heart failure and hypotension. There have been rare reports of flushing.
Gastrointestinal disorders: nausea, vomiting, constipation, ileus and abdominal pain/discomfort. Gingival hyperplasia may occur very rarely when the drug is administered over prolonged periods, and is fully reversible when the drug is discontinued.
Skin and subcutaneous tissue disorders: ankle oedema, Quincke's oedema, Steven-Johnson syndrome, erythema multiforme, erythromelalgia, alopecia and purpura.
Musculoskeletal and connective tissue disorders: muscular weakness, myalgia and arthralgia.
Reproductive system and breast disorders: impotence (erectile dysfunction) has been rarely reported and isolated cases of galactorrhoea. On very rare occasions, gynaecomastia has been observed in elderly male patients under long-term Verapamil treatment, and is fully reversible in all cases when the drug was discontinued.
General disorders and administration site conditions: fatigue.
Investigations: A reversible impairment of liver function characterized by an increase of transaminase and/or alkaline phosphatase may occur on very rare occasions during Verapamil treatment and is most probably a hypersensitivity reaction. Rises in blood prolactin levels have been reported.
4.9 Overdose
The course of symptoms in Verapamil intoxication depends on the amount taken, the point in time at which detoxication measures are taken and myocardial contractility (age related). The main symptoms are as follows: blood pressure fall (at times to values not detectable), shock symptoms, loss of consciousness, 1st and 2nd degree AV block (frequently as Wenckebach’s Phenomenon with or without escape rhythms), total AV block with total AV dissociation, escape rhythm, asystole, bradycardia up to high degree AV block and sinus arrest, hyperglycaemia, stupor and metabolic acidosis. Fatalities have occurred as a result of overdose.
The therapeutic measures to be taken depend on the point in time at which Verapamil was taken and the type and severity of intoxication symptoms. In intoxications with large amounts of slow-release preparations, it should be noted that the release of the active drug and the absorption in the intestine may take more than 48 hours. Verapamil hydrochloride cannot be removed by haemodialysis. Depending on the time of ingestion, it should be taken into account that there may be some lumps of incompletely dissolved tablets along the entire length of the gastro-intestinal tract, which function as active drug depots.
General measures to be taken: gastric lavage with the usual precautions, even later than 12 hours after ingestion, if no gastro-intestinal motility (peristaltic sounds) is detectable. Where intoxication by Vertab SR 240 is suspected, extensive elimination measures are indicated, such as induced vomiting, removal of the content of the stomach and the small intestine under endoscopy, intestinal lavage, laxative, high enemas. The usual intensive resuscitation measures apply, such as extrathoracic heart massage, respiration, defibrillation and/or pacemaker therapy.
Specific measures to be taken: elimination of cardiodepressive effects, hypotension or bradycardia. The specific antidote is calcium, e.g. 10-20 ml of a 10% calcium gluconate solution administered intravenously (2.25-4.5 mmol) repeated if necessary or given as a continuous drip infusion (e.g. 5 mmol/hour).
The following measures may also be necessary: in case of 2nd or 3rd degree AV block, sinus bradycardia, asystole: atropine, isoprenaline, orciprenaline or pacemaker therapy. In case of hypotension: dopamine, dobutamine, noradrenaline. If there are signs of continuing myocardial failure: dopamine, dobutamide, if necessary repeated calcium injections.
5.1 Pharmacodynamic properties
Verapamil, a phenylalkylamine calcium antagonist, has a balanced profile of cardiac and peripheral effects. It lowers heart rate, increases myocardial perfusion and reduces coronary spasm. In a clinical study in patients after myocardial infarction, Verapamil reduced total mortality, sudden cardiac death and reinfarction rate.
Verapamil reduces total peripheral resistance and lowers high blood pressure by vasodilation, without reflex tachycardia. Because of its user-dependent action on the voltage-operated calcium channel, the effects of Verapamil are more pronounced on high than on normal blood pressure.
As early as day one of treatment, blood pressure falls; the effect is found to persist also in long term therapy. Verapamil is suitable for the treatment of all types of hypertension: for monotherapy in mild to moderate hypertension; combined with other antihypertensives (in particular with diuretics and, according to more recent findings, with ACE inhibitors) in more severe types of hypertension. In hypertensive diabetic patients with nephropathy, Verapamil in combination with ACE inhibitors led to a marked reduction of albuminuria and to an improvement of creatinine clearance.
5.2 Pharmacokinetic properties
Absorption: More than 90% of an orally-administered dose of Verapamil is absorbed. Due to an intensive hepatic first-pass metabolism, the absolute bioavailability is about 22% with a variability of about 10 - 35%. Under multiple dosing, bioavailability increases by about 30%. Bioavailability is not affected by food consumption.
Distribution, biotransformation and elimination: Plasma concentrations reach their peak 4 - 8 hours after drug intake. Plasma protein binding of Verapamil is about 90%. The elimination half-life is about 5 - 8 hours. The mean residence time of modified-release Verapamil is 18 hours. After repeated single daily doses, steady-state conditions are reached between 3 - 4 days.
Within 5 days, approximately 70% of an orally-administered dose is excreted in the urine and about 16% with the faeces. Only 3 - 4 % is eliminated renally as unchanged drug. The drug is extensively metabolized. A number of metabolites are generated in humans (twelve have been identified). Of these metabolites only norverapamil has any appreciable pharmacological effect (approximately 20% that of the parent compound, which was observed in a study with dogs). Norverapamil represents about 6% of the dose eliminated in urine. Norverapamil can reach steady-state plasma concentrations approximately equal to those of Verapamil itself. Renal insufficiency does not affect the kinetics of Verapamil.
At-risk patients: In patients with liver cirrhosis, bioavailability is increased and elimination half-life is prolonged. In patients with compensated hepatic insufficiency, no influence on the kinetics of Verapamil was observed.
5.3. Preclinical Safety Data
Verapamil HCl is a well established drug for which there is adequate published safety data. This application is an abridged authorisation application and therefore this data has not been submitted.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Sodium alginate, microcrystalline cellulose, povidone, Hypromellose 2208, colloidal anhydrous silica, and magnesium stearate.
Each tablet contains approximately 32 mg of sodium.
Film coating constituents: Hypromellose 2910, titanium dioxide, Macrogol 400, D&C yellow No. 10 aluminium lake E104, Indigo carmine aluminium lake E132 FD & C blue No 2, carnauba wax.
6.2. Incompatibilities
None.
6.3. Shelf life
60 months.
6.4. Special Precautions for Storage
Store at or below 25 °C.
6.5. Nature and Contents of Container
Blister pack: PVDC-coated-PVC/Aluminium foil.
28 tablets
6.6 Special precautions for disposal
No special requirements.
7 MARKETING AUTHORISATION HOLDER
Dexcel®-Pharma Ltd.
7 Sopwith Way Drayton Fields, Daventry Northamptonshire NN11 8PB UK
8. MARKETING AUTHORISATION NUMBER
PL 14017/0025
OF
9. DATE OF FIRST AUTHORISATION/RENEWAL AUTHORISATION
12th November 1998
10 DATE OF REVISION OF THE TEXT
19/07/2013