This information is intended for use by health professionals

1. Name of the medicinal product

Dilcardia SR 60 mg Prolonged-release capsules, hard

Dilcardia SR 90 mg Prolonged-release capsules, hard

Dilcardia SR 120 mg Prolonged-release capsules, hard

2. Qualitative and quantitative composition

Each capsule contains 60 mg diltiazem hydrochloride.

Each capsule contains 90 mg diltiazem hydrochloride.

Each capsule contains 120 mg diltiazem hydrochloride.

Excipient with known effect:

Each capsule contains up to 30.64 mg of sucrose.

Each capsule contains up to 46 mg of sucrose.

Each capsule contains up to 61.27 mg sucrose.

For the full list of excipients see section 6.1.

3. Pharmaceutical form

Prolonged-release capsule, hard

Size 3, hard gelatin capsule with opaque pink cap and opaque white capsule body, printed with “G” and “DT 60 SR”.

Size 2, hard gelatin capsule with opaque pink cap and opaque yellow capsule body, printed with “G” and “DT 90 SR”.

Size 1, hard gelatin capsule with opaque pink cap and opaque orange capsule body, printed with “G” and “DT 120 SR”.

4. Clinical particulars
4.1 Therapeutic indications

The treatment of angina pectoris.

The treatment of mild to moderate hypertension.

Dilcardia SR capsules are indicated for use in adults only.

4.2 Posology and method of administration



Adults: the usual initial dose is 90 mg twice daily. Dosage may be increased gradually to 120 mg twice daily or 180 mg twice daily if required. Patients' responses may vary and dosage requirements can differ significantly between individual patients.


Adults: the usual dose is 120 mg once or twice daily. Patients may benefit by titrating from a lower total daily dose.

Paediatric population

The safety and efficacy in children has not been established. Therefore diltiazem is not recommended for use in children.

Dosage in the elderly and patients with impaired hepatic or renal function


Dosage should commence at 60 mg twice daily and the dose carefully titrated as required.


Dosage should commence at the lower level of 60 mg twice daily and be increased slowly in order to achieve the required level of control. The daily dose should not exceed 90 mg twice daily. Do not increase the dose if the heart rate falls below 50 beats per minute.

Method of administration

For oral use.

Capsules should be swallowed whole with water and should not be sucked, chewed or crushed.

4.3 Contraindications

▪ Hypersensitivity to diltiazem hydrochloride or to any of the excipients listed in section 6.1

▪ Pregnancy and in women of child bearing potential

▪ Severe bradycardia (below 40 bpm)

▪ Second- or third-degree AV block except in the presence of a functioning ventricular pacemaker

▪ Sick sinus syndrome except in the presence of a functioning ventricular pacemaker

▪ Cardiac failure after myocardial infarction

▪ Left ventricular failure with pulmonary congestion

▪ Concomitant administration of dantrolene infusion (see section 4.5)

▪ Combination with ivabradine (see section 4.5)

4.4 Special warnings and precautions for use

Rare instances of hyperglycaemia have been reported in association with diltiazem hydrochloride. The use of diltiazem in diabetic patients may require adjustment of their control.

Precaution should be taken in patients with reduced left ventricular function. Patients should be observed closely if they have bradycardia (risk of exacerbation), first degree AV block detected on the electrocardiogram (risk of exacerbation and rarely, of complete block) or prolonged PR interval.

Diltiazem is considered unsafe in patients with acute porphyria.

Prior to general anaesthesia, the anaesthetist must be informed of ongoing diltiazem treatment. Depression of cardiac contractility, conductivity and automaticity, as well as the vascular dilatation associated with anaesthetics may be potentiated by calcium channel blockers.

Increase of plasma concentrations of diltiazem may be observed in the elderly and in patients with renal or hepatic insufficiency. The contraindications and precautions should be carefully observed and close monitoring, particularly of heart rate, should be carried out at the beginning of treatment.

Calcium channel blocking agents, such as diltiazem, may be associated with mood changes, including depression.

Like other calcium channel antagonists, diltiazem has an inhibitory effect on intestinal motility. Therefore it should be used with caution in patients at risk to develop an intestinal obstruction. Tablet residues from slow release formulations of the product may pass into the patient's stools; however, this finding has no clinical relevance.

Patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption or sucrase-isomaltase insufficiency should not take this medicine.

4.5 Interaction with other medicinal products and other forms of interaction

Concomitant use contraindicated:

Dantrolene (infusion): Lethal ventricular fibrillation is regularly observed in animals when intravenous verapamil and dantrolene are administered concomitantly. The combination of a calcium antagonist and dantrolene is therefore potentially dangerous (see section 4.3).

Concomitant use requiring caution:

Lithium: Risk of increase in lithium-induced neurotoxicity.

Nitrate derivatives: Increased hypotensive effects and faintness (additive vasodilatating effects): In all the patients treated with calcium antagonists, the prescription of nitrate derivatives should only be carried out at gradually increasing doses.

Theophylline: Increase in circulating theophylline levels.

Alpha-antagonists: Increased antihypertensive effects:

Concomitant treatment with alpha-antagonists may produce or aggravate hypotension. The combination of diltiazem with an alpha-antagonist should be considered only with the strict monitoring of the blood pressure.

Amiodarone, digoxin: Increased risk of bradycardia:

Caution is required when these are combined with diltiazem, particularly in elderly subjects and when high doses are used. Diltiazem hydrochloride may cause small increases in plasma levels of digoxin, requiring careful monitoring of AV conduction.

Beta-blockers: Possibility of rhythm disturbances (pronounced bradycardia, sinus arrest), sino-atrial and atrio-ventricular conduction disturbances and heart failure (synergistic effect). Patients with pre-existing conduction defects should not receive the combination of diltiazem and beta-blockers.Such a combination must only be used under close clinical and ECG monitoring, particularly at the beginning of treatment.

Other hypertensive drugs: Enhanced antihypertensive effect may occur with concomitant use of other hypertensive drugs (e.g. beta-blockers, diuretics, ACE-inhibitors) or drugs that cause hypotension such as aldesleukin and antipsychotics.

Combination with beta-adrenoceptor blockers having significant "first pass" loss, e.g. propranolol, may require a decrease in their dose. Diltiazem will not protect against effects of withdrawal of beta-adrenoceptor blocking agents, nor the rebound effects seen with various antihypertensives.

Other antiarrhythmic agents:

Since diltiazem has antiarrhythmic properties, its concomitant prescription with other antiarrhythmic agents is not recommended (additive risk of increased cardiac adverse effects). This combination should only be used under close clinical and ECG monitoring.

Carbamazepine: Increase in circulating carbamazepine levels:

It is recommended that the plasma carbamazepine concentrations be assayed and that the dose should be adjusted if necessary.

Rifampicin: Risk of decrease of diltiazem plasma levels after initiating therapy with rifampicin: The patient should be carefully monitored when initiating or discontinuing rifampicin treatment.

Anti-H2 agents (cimetidine, ranitidine): Increase in plasma diltiazem concentrations.

Patients currently receiving diltiazem therapy should be carefully monitored when initiating or discontinuing therapy with anti-H2 agents. An adjustment in diltiazem daily dose may be necessary.

Protease inhibitors (e.g. atazanavir, ritonavir): Increase in plasma diltiazem concentrations.

Ciclosporin: Increase in circulating ciclosporin levels:

It is recommended that the ciclosporin dose be reduced, renal function be monitored, circulating ciclosporin levels be assayed and that the dose should be adjusted during combined therapy and after its discontinuation.

General information to be taken into account:

Diltiazem has been continued in anaesthesia without problems, but the anaesthetist should be made aware that the patient is taking this medication because of the potential for synergism or interactions with other agents used in anaesthesia (see section 4.4).

Due to the potential for additive effects, caution and careful titration are necessary in patients receiving diltiazem concomitantly with other agents known to affect cardiac contractility and/or conduction.

Diltiazem is metabolized by CYP3A4. A moderate (less than 2-fold) increase of diltiazem plasma concentration in cases of co-administration with a stronger CYP3A4 inhibitor has been documented. Diltiazem is also a CYP3A4 isoform inhibitor. Co-administration with other CYP3A4 substrates may result in an increase in plasma concentration of either co-administered drug (e.g. cilostazol, ivabradine, sirolimus, tacrolimus). Care should be exercised in patients taking these drugs. Concomitant use of diltiazem with cilostazol should be avoided. Co-administration of diltiazem with a CYP3A4 inducer may result in a decrease of diltiazem plasma concentrations.

Concomitant use of diltiazem with ivabradine is contraindicated due to the additional heart rate lowering effect of diltiazem to ivabradine (see section 4.3).

Barbiturates (phenobarbital, primidone) serum levels of diltiazem may be decreased by concomitant usage of CYP34A inducers.

Phenytoin: serum levels of diltiazem may be decreased by concomitant use of CYP34A inducers. Diltiazem may increase serum levels of phenytoin.

Benzodiazepines (midazolam, triazolam): Diltiazem significantly increases plasma concentrations of midazolam and triazolam and prolongs their half-life. Special care should be taken when prescribing short-acting benzodiazepines metabolised by the CYP3A4 pathway in patients using diltiazem.

Diltiazem may increase bioavailability of tricyclic antidepressants.

Corticosteroids (methylprednisolone): Inhibition of methylprednisolone metabolism (CYP3A4) and inhibition of P-glycoprotein: The patient should be monitored when initiating methylprednisolone treatment. An adjustment in the dose of methylprednisolone may be necessary.

Statins (simvastatin, atorvastatin, lovastatin): Diltiazem is an inhibitor of CYP3A4 and has been shown to significantly increase the AUC of some statins. The risk of myopathy and rhabdomyolysis due to statins metabolised by CYP3A4 may be increased with concomitant use of diltiazem. When possible, a non CYP3A4-metabolised statin should be used together with diltiazem, otherwise close monitoring for signs and symptoms of a potential statin toxicity is required.

Dilcardia SR capsules should not be taken at the same time as alcohol, as it may increase the rate of release of diltiazem from the prolonged release preparation. In addition the combination of alcohol and diltiazem may have an additive vasodilatory effect.

4.6 Fertility, pregnancy and lactation


There is very limited data from the use of diltiazem in pregnant patients. Diltiazem has been shown to have reproductive toxicity in certain animal species (rat, mice, rabbit). Diltiazem is contraindicated during pregnancy (see section 4.3), as well as in women of child-bearing potential not using effective contraception.


Diltiazem is excreted in breast milk at low concentrations. Breast-feeding while taking this drug should be avoided. If use of diltiazem is considered medically essential, an alternative method of infant feeding should be instituted.

4.7 Effects on ability to drive and use machines

On the basis of reported adverse drug reactions, i.e. dizziness (common), malaise (common), the ability to drive and use machines could be altered. However, no studies have been performed.

4.8 Undesirable effects

The following CIOMS frequency rating is used, when applicable: Very common (≥1/10); common (≥1/100 to <1/10); uncommon (≥1/1,000 to ≤1/100); rare (≥1/10,000 to ≤1/1,000); very rare (≤1/10,000); not known (cannot be estimated from the available data).

Within each frequency grouping, adverse events are presented in order of decreasing seriousness.

Very Common




Not Known

Blood and lymphatic system disorders


Immune system disorders


Psychiatric disorders

Nervousness, insomnia

Mood changes (including depression), anorexia

Nervous system disorders

Headache, dizziness

Extrapyramidal syndrome, Parkinsonian syndrome, paraesthesia

Cardiac disorders

Atrioventricular block (may be of first, second or third degree; bundle branch block may occur), palpitations


Sinoatrial block, congestive heart failure

Vascular disorders


Orthostatic hypotension

Vasculitis (including leukocytoclastic vasculitis)


Gastrointestinal disorders

Constipation, dyspepsia, gastric pain, nausea

Vomiting, diarrhoea

Dry mouth

Gingival hyperplasia

Gastrointestinal disorder

Hepatobiliary disorders

Hepatic enzymes increase (AST, ALT, LDH, ALP increase)


Skin and subcutaneous tissue disorders

Erythema, pruritus


Photosensitivity (including lichenoid keratosis at sun exposed skin areas), angioneurotic oedema, rash, erythema multiforme (including Steven-Johnson's syndrome and toxic epidermal necrolysis), sweating, exfoliative dermatitis, acute generalised exanthematous pustulosis, desquamative erythema with or without fever, allergic dermatitis hyperpigmentation

Reproductive system and breast disorders


General disorders and administration site conditions

Peripheral oedema

Malaise, fatigue

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 the Yellow Card Scheme at or search for MHRA Yellow Card in the Google Play or Apple App Store.

4.9 Overdose


The clinical effects of acute overdose can involve pronounced hypotension possibly leading to collapse, sinus bradycardia with or without isorhythmic dissociation, and atrioventricular conduction disturbances. It is recommended that patients with suspected overdose should be placed under observation in a coronary care unit.

Most patients suffering from overdosage of diltiazem become hypotensive within 8 hours of ingestion. With bradycardia and first to third degree atrioventricular block also developing, cardiac arrest may ensue. Hyperglycaemia is also a recognised complication. The elimination half-life of diltiazem after overdosage is estimated to be about 5.5-10.2 hours.

The following may be linked to renal impairment in patients; polyuri, pollakiuria, nocturia, acute kidney injury, acute interstitiel nephritis.


Treatment, in a hospital setting, will include gastric lavage with administration of activated charcoal to reduce diltiazem absorption and/or osmotic diuresis. Conduction disturbances may be managed by temporary cardiac pacing. Proposed corrective treatments: Hypotension should be corrected with plasma expanders, vasopressors, glucagon, calcium gluconate infusion and inotropic agents (e.g. dopamine, dobutamine or isoprenaline). Symptomatic bradycardia and high grade AV block may respond to atropine, isoprenaline or occasionally cardiac pacing which may be useful if cardiac standstill occurs.

Dilcardia SR capsules are prolonged release capsules and effects may be slow in onset and prolonged, therefore, monitoring should be carried out for longer periods than following overdose with immediate-release dosage forms.

5. Pharmacological properties
5.1 Pharmacodynamic properties

Pharmacotherapeutic group: Selective calcium channel blockers with direct cardiac effects:

ATC code: C08DB01

Diltiazem hydrochloride is a calcium-channel blocking agent. It is a peripheral and coronary vasodilator with some negative inotropic activity. Diltiazem inhibits cardiac conduction particularly at the sino-atrial and atrioventricular nodes. It is used in the management of classical and vasospastic angina pectoris and it is also used in the treatment of essential hypertension.

5.2 Pharmacokinetic properties


Diltiazem is rapidly and almost completely absorbed from the gastro-intestinal tract following oral administration, but undergoes extensive first-pass hepatic metabolism. The bioavailability has been reported to be about 40%, although there is considerable inter-individual variation in plasma concentrations.


Diltiazem is about 80% bound to plasma proteins.


It is extensively metabolised in the liver; one of the metabolites, desacetyl diltiazem has been reported to have 25 to 50% of the activity of the parent compound. The half-life is reported to be about 3 to 4 hours.


Approximately 60% of the dose is excreted in the bile and 35 to 40% in the urine, and 2 to 4% as unchanged diltiazem.

The prolonged-release formulation is designed for twice daily dosage.

5.3 Preclinical safety data

There are no additional data of relevance to the prescriber.

6. Pharmaceutical particulars
6.1 List of excipients

Capsule contents

Sugar spheres (up to 92 % sucrose)


Methacrylic acid – ethyl acrylate copolymer


Diethyl phthalate


Capsule shell


Titanium dioxide (E171)

Red iron oxide (E172)

Yellow iron oxide (E172) (90 mg and 120 mg capsules only)



Iron oxide black (E172)

Propylene glycol

Ammonium hydroxide/Strong ammonia solution

and may also contain potassium hydroxide

6.2 Incompatibilities

Not applicable.

6.3 Shelf life

4 years

6.4 Special precautions for storage

Store below 25°C. Store in the original package in order to protect from moisture.

6.5 Nature and contents of container

PVC/aluminium foil blister strips (enclosed in outer cardboard cartons) containing 56 capsules.

Polyethylene containers with polypropylene caps containing 100 capsules.

6.6 Special precautions for disposal and other handling

No special requirements.

7. Marketing authorisation holder

Generics [UK] Limited t/a Mylan

Station Close

Potters Bar



United Kingdom

8. Marketing authorisation number(s)

PL 04569/0350

PL 04569/0351

PL 04569/0352

9. Date of first authorisation/renewal of the authorisation

Date of first authorisation: 29/10/1997

Renewal of the authorisation: 23/04/2008

10. Date of revision of the text

21 March 2018