Amlodipine 5mg Tablets
Out of date information, search anotherSUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Amlodipine 5 mg Tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains amlodipine besilate equivalent to 5mg of amlodipine.
For excipients see section 6.1.
3 PHARMACEUTICAL FORM
Tablet.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
• Hypertension.
• Prophylaxis of chronic stable angina pectoris.
• Prinzmetal's (variant) angina when diagnosed by a cardiologist.
• In hypertensive patients, Amlodipine has been used in combination with a thiazide diuretic, alphablocker, beta-adrenoceptor blocking agent, or an angiotensin converting enzyme inhibitor.
• For angina, Amlodipine Tablets may be used as monotherapy or in combination with other antianginal drugs in patients with angina that is refractory to nitrates and/or adequate doses of beta blockers.
• Amlodipine is well tolerated in patients with heart failure and a history of hypertension or ischaemic heart disease.
4.2 Posology and method of administration
In adults
For both hypertension and angina the usual initial dose is 5mg Amlodipine Tablets once daily which may be increased to a maximum dose of 10mg depending on the individual patient's response.
No dose adjustment of Amlodipine Tablets is required upon concomitant administration of thiazide diuretics, beta blockers, and angiotensin-converting enzyme inhibitors.
Use in children
Children with hypertension from 6 years to 17 years of age.
The recommended antihypertensive oral dose in pediatric patients ages 6-17 years is 2.5 mg once daily as a starting dose, up-titrated to 5 mg once daily if blood pressure goal is not achieved after 4 weeks. Doses in excess of 5 mg daily have not been studied in pediatric patients (see section 5.1 Pharmacodynamic Properties and section 5.2 Pharmacokinetic Properties).
The effect of amlodipine on blood pressure in patients less than 6 years of age is not known.
For capsules or tablets without a break-line: The 2.5 mg dose cannot be obtained with Amlodipine tablets 5 mg & 10 mg as these tablets are not manufactured to break into two equal halves.
Use in the elderly
Amlodipine Tablets, used at similar doses in elderly or younger patients, is equally well tolerated. Therefore normal dosage regimens are recommended.
Patients with hepatic impairment
See section 4.4 "Special warnings and special precautions for use".
Patients with renal impairment
Changes in amlodipine plasma concentrations are not correlated with degree of renal impairment, therefore the normal dosage is recommended. Amlodipine is not dialysable.
4.3 Contraindications
• Amlodipine Tablets are contra-indicated in patients with a known sensitivity to dihydropyridines, amlodipine or any of the excipients.
• Amlodipine Tablets should not be used in cardiogenic shock, clinically significant aortic stenosis, unstable angina (excluding Prinzmetal's angina).
• Pregnancy and lactation.
4.4 Special warnings and precautions for use
In a long term, placebo-controlled study, in patients with NYHA III and IV heart failure of non-ischaemic aetiology, amlodipine was associated with increased reports of pulmonary oedema despite no significant difference in the incidence of worsening heart failure as compared to placebo. See section 5.1.
Use in patients with impaired hepatic function
As with all calcium antagonists, amlodipine's half-life is prolonged in patients with impaired liver function and dosage recommendations have not been established. The drug should therefore be administered with caution in these patients. There are no data to support the use of Amlodipine Tablets alone, during or within one month of a myocardial infarction. The safety and efficacy of Amlodipine Tablets in hypertensive crisis has not been established.
4.5 Interaction with other medicinal products and other forms of interaction
Amlodipine has been safely administered with thiazide diuretics, alpha blockers, beta blockers, angiotensin-converting enzyme inhibitors, long-acting nitrates, sublingual glyceryl trinitrate, non-steroidal anti-inflammatory drugs, antibiotics, and oral hypoglycaemic drugs.
In vitro data from studies with human plasma, indicate that amlodipine has no effect on protein binding of digoxin, phenytoin, warfarin or indomethacin.
Caution should be exercised in combination of amlodipine and CYP3A4 inhibitors and CYP3A4 inducers.
Special Studies: Effects of other agents on amlodipine
Cimetidine: Co-administration of amlodipine with cimetidine did not alter the pharmacokinetics of amlodipine.
Grapefruit juice: Co-administration of 240ml of grapefruit juice with a single oral dose of amlodipine 10mg in healthy volunteers had no significant effect on the pharmacokinetics of amlodipine.
Sildenafil: When sildenafil and amlodipine were used in combination, each agent independently exerted its own blood pressure lowering effect.
Special Studies: Effect of amlodipine on other agents.
Atorvastatin: Co-administration of multiple 10mg doses of amlodipine with 80mg of atorvastatin resulted in no significant change in the steady state pharmacokinetic parameters of atorvastatin.
Digoxin: Co-administration of amlodipine with digoxin did not change digoxin levels or digoxin renal clearance in normal volunteers.
Warfarin: In healthy male volunteers, the co-administration of amlodipine does not significantly alter the effect of warfarin on prothrombin response time. Coadministration of amlodipine with warfarin did not change the warfarin prothrombin response time.
Ciclosporin: Pharmacokinetic studies with ciclosporin have demonstrated that amlodipine does not significantly alter the pharmacokinetics of ciclosporin.
Drug/Laboratory test interactions: None known.
4.6 Pregnancy and lactation
Although some dihydropyridine compounds have been found to be teratogenic in animals, data in the rat and rabbit for amlodipine provide no evidence for a teratogenic effect. There is, however, no clinical experience with the preparation in
pregnancy or lactation. Accordingly, Amlodipine Tablets should not be administered during pregnancy, or lactation, or to women of childbearing potential unless effective contraception is used.
4.7 Effects on ability to drive and use machines
Clinical experience with Amlodipine indicates that therapy is unlikely to impair a patient's ability to drive or use machinery. In patients suffering from dizziness, headache, fatigue or nausea the ability to react may be impaired.
4.8 Undesirable effects
Adverse events that have been reported in amlodipine trials are categorised below, according to system organ class and frequency. Frequencies are defined as: very common (>10%); common (>1%, <10%); uncommon (>0.1%, <1%); rare (>0.01%, <0.1%) and very rare (<0.01%).
|
Blood and the Lymphatic System Disorders |
thrombocytopenia |
Very Rare |
|
Immune System Disorders |
allergic reaction |
Very Rare |
|
Metabolism and Nutrition Disorders |
hyperglycaemia |
Very Rare |
|
Psychiatric Disorders |
insomnia, mood changes |
Uncommon |
|
Nervous System Disorders |
somnolence, dizziness, headache |
Common |
|
tremor, taste perversion, syncope, hypoaesthesia, paraesthesia |
Uncommon | |
|
peripheral neuropathy |
Very Rare | |
|
Eye Disorders |
visual disturbances |
Uncommon |
|
Ear and Labyrinth Disorders |
tinnitus |
Uncommon |
|
Cardiac Disorders |
palpitations |
Common |
|
myocardial infarction, arrhythmia, ventricular tachycardia and atrial fibrillation) |
Very rare | |
|
Vascular Disorders |
flushing |
Common |
|
hypotension |
Uncommon | |
|
vasculitis |
Very Rare |
|
Respiratory, Thoracic and Mediastinal Disorders |
dyspnoea, rhinitis coughing |
Uncommon Very Rare |
|
Gastrointestinal Disorders |
abdominal pain, nausea |
Common |
|
vomiting, dyspepsia, altered bowel habits, dry mouth |
Uncommon | |
|
pancreatitis, gastritis, gingival hyperplasia |
Very Rare | |
|
Hepato-biliary Disorders |
hepatitis, jaundice and hepatic enzyme elevations (mostly consistent with cholestasis) |
Very Rare |
|
Skin and Subcutaneous Tissue Disorders |
alopecia, purpura, skin discolouration, increased sweating, pruritus, rash |
Uncommon |
|
angioedema, erythema multiforme, urticaria |
Very Rare | |
|
Musculoskeletal and Connective Tissue Disorders |
arthralgia, myalgia, muscle cramps, back pain |
Uncommon |
|
Renal and Urinary Disorders |
micturition disorder, nocturia, increased urinary frequency |
Uncommon |
|
Reproductive System and Breast Disorders |
impotence, gynaecomastia |
Uncommon |
|
General Disorders and Administration Site Conditions |
oedema, fatigue |
Common |
|
chest pain, asthenia, pain, malaise |
Uncommon | |
|
Investigations |
weight increase, weight decrease |
Uncommon |
4.9 Overdose
Available data suggest that gross overdosage could result in excessive peripheral vasodilatation and possibly reflex tachycardia. Marked and probably prolonged systemic hypotension up to and including shock with fatal outcome have been reported. Administration of activated charcoal to healthy volunteers immediately or up to two hours after ingestion of amlodipine 10mg has been shown to significantly decrease amlodipine absorption. Gastric lavage may be worthwhile in some cases. Clinically significant hypotension due to amlodipine overdosage calls for active cardiovascular support including frequent monitoring of cardiac and respiratory function, elevation of extremities, and attention to circulating fluid volume and urine output. A vasoconstrictor may be helpful in restoring vascular tone and blood pressure, provided that there is no contraindication to its use. Intravenous calcium gluconate may be beneficial in reversing the effects of calcium channel blockade. Since amlodipine is highly protein-bound, dialysis is not likely to be of benefit.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Antihypertensive agents, Calcium antagonist.
ATC-Code: C08CA01
Amlodipine Tablets is a calcium ion influx inhibitor of the dihydropyridine group (slow channel blocker or calcium ion antagonist) and inhibits the transmembrane influx of calcium ions into cardiac and vascular smooth muscle.
The mechanism of the antihypertensive action of Amlodipine Tablets is due to a direct relaxant effect on vascular smooth muscle. The precise mechanism by which Amlodipine Tablets relieves angina has not been fully determined but Amlodipine Tablets reduces total ischaemic burden by the following two actions.
• Amlodipine Tablets dilates peripheral arterioles and thus, reduces the total peripheral resistance (afterload) against which the heart works. Since the heart rate remains stable, this unloading of the heart reduces myocardial energy consumption and oxygen requirements.
• The mechanism of action of Amlodipine Tablets also probably involves dilatation of the main coronary arteries and coronary arterioles, both in normal and ischaemic regions. This dilatation increases myocardial oxygen delivery in patients with coronary artery spasm (Prinzmetal's or variant angina).
In patients with hypertension, once daily dosing provides clinically significant reductions of blood pressure in both the supine and standing positions throughout the 24 hour interval.
Due to the slow onset of action, acute hypotension is not a feature of Amlodipine administration.
In patients with angina, once daily administration of Amlodipine increases total exercise time, time to angina onset, and time to 1mm ST segment depression, and decreases both angina attack frequency and glyceryl trinitrate tablet consumption.
Amlodipine has not been associated with any adverse metabolic effects or changes in plasma lipids and is suitable for use in patients with asthma, diabetes, and gout.
Use in Patients with Heart failure: Haemodynamic studies and exercise based controlled clinical trials in NYHA Class II - IV heart failure patients have shown that Amlodipine did not lead to clinical deterioration as measured by exercise tolerance, left ventricular ejection fraction and clinical symptomatology.
A placebo controlled study (PRAISE) designed to evaluate patients in NYHA Class III - IV heart failure receiving digoxin, diuretics and ACE inhibitors has shown that Amlodipine did not lead to an increase in risk of mortality or combined mortality and morbidity with heart failure.
In a follow-up, long term, placebo controlled study (PRAISE-2) of amlodipine in patients with NYHA III and IV heart failure without clinical symptoms or objective findings suggestive of underlying ischaemic disease, on stable doses of ACE inhibitors, digitalis and diuretics, amlodipine had no effect on total cardiovascular mortality. In the same population amlodipine was associated with increased reports of pulmonary oedema despite no significant difference in the incidence of worsening heart failure as compared to placebo.
Paediatric Population
In a study involving 268 children aged 6-17 years with predominantly secondary hypertension, comparison of a 2.5mg dose, and 5.0mg dose of amlodipine with placebo, showed that both doses reduced Systolic Blood Pressure significantly more than placebo. The difference between the two doses was not statistically significant.
The long-term effects of amlodipine on growth, puberty and general development have not been studied.
The long-term efficacy of amlodipine on therapy in childhood to reduce cardiovascular morbidity and mortality in adulthood have also not been established.
5.2 Pharmacokinetic properties
Absorption, distribution, plasma protein binding
After oral administration of therapeutic doses, amlodipine is well absorbed with peak blood levels between 6-12 hours post dose. Absolute bioavailability has been estimated to be between 64 and 80%. The volume of distribution is approximately 21 l/kg. In vitro studies have shown that approximately 97.5% of circulating amlodipine is bound to plasma proteins.
Biotransformation/elimination
The terminal plasma elimination half life is about 35-50 hours and is consistent with once daily dosing. Amlodipine is extensively metabolised by the liver to inactive metabolites with 10% of the parent compound and 60% of metabolites excreted in the urine.
Paediatric Population
A population PK study has been conducted in 74 hypertensive children aged from 1 month to 17 years (with 34 patients aged 6 to 12 years and 28 patients aged 13 to 17 years) receiving amlodipine between 1.25 and 20 mg given either once or twice daily. In children 6 to 12 years and in adolescents 13-17 years of age the typical oral clearance (CL/F) was 22.5 and 27.4 L/hr respectively in males and 16.4 and 21.3 L/hr respectively in females. Large variability in exposure between individuals was observed. Data reported in children below 6 years is limited.
Use in the elderly
The time to reach peak plasma concentrations of amlodipine is similar in elderly and younger subjects. Amlodipine clearance tends to be decreased with resulting increases in AUC and elimination half-life in elderly patients. Increases in AUC and elimination half-life in patients with congestive heart failure were as expected for the patient age group studied.
5.3 Preclinical safety data
None
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Microcrystalline Cellulose,
Dibasic Calcium Phosphate Anhydrous,
Sodium Starch Glycollate and Magnesium Stearate.
6.2 Incompatibilities
None stated.
6.3 Shelf life
24 months
6.4 Special precautions for storage
None specified.
6.5 Nature and contents of container
Amlodipine Tablets is available as:
Packs of 28 tablets. Aluminium/PVC/PVDC blister strips, 14 tablets/strip, 2 strips in a carton box.
6.6 Special precautions for disposal
No special requirements.
7 MARKETING AUTHORISATION HOLDER
Pramod Rajani Organisation Limited
Foster Avenue, unit 5, Aragon Park
Dunstable
Bedfordshire
LU5 5TA
UK
8 MARKETING AUTHORISATION NUMBER(S)
PL 22083/0001
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
25/09/2007
10 DATE OF REVISION OF THE TEXT
20/04/2011