Summary of Product Characteristics Updated 06-Apr-2020 | Rosemont Pharmaceuticals Limited
Propranolol Rosemont 10mg/5ml Oral Solution
Propranolol Hydrochloride 10mg/5ml
Excipients with known effect:
Methyl parahydroxybenzoate (E218) 6mg/5ml
Propyl parahydroxybenzoate (E216) 1.5mg/5ml
Liquid maltitol (E965) 3000mg/5ml
Propylene glycol (E1520) 100mg/5ml
For the full list of excipients, see Section 6.1.
Clear colourless liquid with odour of orange/tangerine.
Propranolol is indicated in:
- the control of hypertension
- the management of angina pectoris
- the long term prophylaxis against reinfarction after recovery from acute myocardial infarction
- the control of most forms of cardiac arrhythmia
- the prophylaxis of migraine
- the management of essential tremor
- relief of situational anxiety and generalised anxiety symptoms, particularly those of the somatic type
- prophylaxis of upper gastro-intestinal bleeding in patients with portal hypertension and oesophageal varices
- the adjunctive management of thyrotoxicosis and thyrotoxic crisis
- management of hypertrophic obstructive cardiomyopathy
- management of phaeochromocytoma perioperatively (with an alpha-adrenoceptor blocking drug)
Hypertension – A starting dose of 80mg twice a day may be increased at weekly intervals according to response. The usual dose range is 160 – 320mg per day. With concurrent diuretic or other antihypertensive drugs a further reduction of blood pressure is obtained.
Angina, migraine and essential tremor – A starting dose of 40mg two or three times daily may be increased by the same amount at weekly intervals according to patient response. An adequate response in migraine and essential tremor is usually seen in the range 80-160mg/day and in angina in the range 120-240mg/day.
Situational and generalised anxiety – A dose of 40mg daily may provide short term relief of acute situational anxiety. Generalised anxiety, requiring longer term therapy, usually responds adequately to 40mg twice daily which, in individual cases, may be increased to 40mg three times daily. Treatment should be continued according to response. Patients should be reviewed after six to twelve months treatment.
Arrhythmias, anxiety, tachycardia, hypertrophic obstructive cardiomyopathy and thyrotoxicosis – A dosage range of 10-40mg three or four times a day usually achieves the required response.
Post myocardial infarction - Treatment should start between days 5 and 21 after myocardial infarction with an initial dose of 40mg four times a day for 2 or 3 days. In order to improve compliance the total daily dosage may thereafter be given as 80mg twice daily.
Dosage should be titrated to achieve approximately 25% reduction in resting heart rate. Dosage should begin with 40mg twice daily, increasing to 80mg twice daily depending on heart rate response. If necessary, the dose may be increased incrementally to a maximum of 160mg twice daily.
Phaeochromocytoma (Used only with an alpha-receptor blocking drug)- Pre-operative: 60mg daily for three days is recommended. Non-operable malignant cases: 30mg daily.
Evidence concerning the relation between blood level and age is conflicting. Propranolol should be used to treat the elderly with caution. It is suggested that treatment should start with the lowest dose.
The optimum dose should be individually determined according to the clinical response.
Arrhythmias, phaeochromocytoma, thyrotoxicosis – Dosage should be individually determined and the following is only a guide: 250 – 500 micrograms per kilogram three or four times daily as required.
Migraine – Under the age of 12: 20mg two or three times daily
Over the age of 12: the adult dose
Fallot's tetralogy – The value of propranolol in this condition is confined mainly to the relief of right-ventricular outflow tract shut-down. It is also useful for treatment of associated arrhythmias and angina. Dosage should be individually determined and the following is only a guide: Up to 1mg/Kg repeated three or four times a day as required..
Method of administration
For oral administration only.
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
Propranolol must not be used if there is a history of bronchial asthma or bronchospasm.
The product label states the following warning: “Do not take propranolol if you have a history of asthma or wheezing”. A similar warning appears in the patient information leaflet.
Bronchospasm can usually be reversed by beta2-agonist bronchodilators such as salbutamol. Large doses of the beta2-agonist bronchodilator may be required to overcome the beta-blockade produced by propranolol and the dose should be titrated according to the clinical response; both intravenous and inhalational administration should be considered. The use of intravenous aminophylline and/or the use of ipratropium (given by nebuliser) may also be considered. Glucagon (1 to 2mg given intravenously) has also been reported to produce a bronchodilator effect in asthmatic patients. Oxygen or artificial ventilation may be required in severe cases.
Propranolol as with other beta-adrenoceptor blocking drugs must not be used in patients with any of the following:
hypersensitivity to propranolol hydrochloride or any of the ingredients; the presence of second or third degree heart block; in cardiogenic shock; metabolic acidosis; after prolonged fasting; bradycardia; hypotension; severe peripheral arterial circulatory disturbances; sick sinus syndrome; untreated phaeochromocytoma; uncontrolled heart failure or Prinzmetal's angina.
Propranolol must not be used in patients prone to hypoglycaemia, i.e., patients after prolonged fasting or patients with restricted counter-regulatory reserves. Patients with restricted counter-regulatory reserves may have reduced autonomic and hormonal responses to hypoglycaemia which includes glycogenolysis, gluconeogenesis and /or impaired modulation of insulin secretion. Patients at risk for an inadequate response to hypoglycaemia includes individuals with malnutrition, prolonged fasting, starvation, chronic liver disease, diabetes and concomitant use of drugs which block the full response to catecholamines.
Although contra-indicated in uncontrolled heart failure (see section 4.3), propranolol may be used where the signs of heart failure have been controlled by the use of appropriate concomitant medication. Propranolol should be used with caution in patients whose cardiac reserve is poor.
Treatment should not be discontinued abruptly in patients with ischaemic heart disease. Either the equivalent dose of another beta-adrenoceptor blocking drug may be substituted or the withdrawal of propranolol should be gradual over a period of 7 to 14 days. Patient should be followed during withdrawal especially those with ischaemic heart disease.
Propranolol should not be used in combination with calcium channel blockers with negative inotropic effects (e.g. verapamil, diltiazem), as it can lead to an exaggeration of these effects particularly in patients with impaired ventricular function and/or SA or AV conduction abnormalities. This may result in severe hypotension, bradycardia and cardiac failure. Neither the beta-blocker nor the calcium channel blocker should be administered intravenously within 48 hours of discontinuing the other.
Propranolol may block/modify the signs and symptoms of hypoglycaemia (especially tachycardia). Propranolol occasionally causes hypoglycaemia, even in non-diabetic patients, e.g., neonates, infants, children, elderly patients, patients on haemodialysis or patients suffering from chronic liver disease and patients suffering from overdose. Severe hypoglycaemia associated with propranolol has rarely presented with seizures and/or coma in isolated patients. Caution must be exercised in the concurrent use of propranolol and hypoglycaemic therapy in diabetic patients. Propranolol may prolong the hypoglycaemic response to insulin (see section 4.3).
When a patient is scheduled for surgery and a decision is made to discontinue beta-blocker therapy, this should be done at least 24 hours prior to the procedure. The risk/benefit of stopping beta blockade should be made for each patient
Propranolol should not be used in untreated phaeochromocytoma. However, in patients with phaeochromocytoma, an alpha-blocker may be given concomitantly.
Although contra-indicated in severe peripheral arterial circulatory disturbances (see section 4.3), propranolol may also aggravate less severe peripheral arterial circulatory disturbances.
One of the pharmacological actions of propranolol is to reduce the heart rate. Therefore the dosage should be reduced in those rare cases where symptoms are attributable to a slow heart rate.
Due to propranolol having a negative effect on conduction time, caution must be exercised if it is given to patients with first degree heart block.
Since the half life may be increased in patients with significant hepatic or renal impairment, caution must be exercised when starting treatment and selecting the initial dose.
In patients with portal hypertension, liver function may deteriorate and hepatic encephalopathy may develop. There have been reports suggesting that treatment with propranolol may increase the risk of developing hepatic encephalopathy (see section 4.2).
Propranolol may cause a more severe reaction to a variety of allergens, when given to patients with a history of anaphylactic reaction to such allergens. Such patients may be unresponsive to the usual doses of adrenaline used to treat the allergic reactions.
Propranolol may mask the signs of thyrotoxicosis.
Propranolol must be used with caution in patients with decompensated cirrhosis (see section 4.2).
Propranolol should be used to treat the elderly with caution starting with a lower dose (see section 4.2)
Laboratory Tests: Propranolol has been reported to interfere with the estimation of serum bilirubin by the diazo method and with the determination of catecholamines by methods using fluorescence.
This product contains:
- parahydroxybenzoates which may cause allergic reactions (possibly delayed).liquid maltitol. Patients with rare hereditary problems of fructose intolerance should not take this medicine
- Propylene glycol 20 mg in each ml.
- Co-administration with any substrate for alcohol dehydrogenase such as ethanol may induce adverse effects in children less than 5 years old.
- While propylene glycol has not been shown to cause reproductive or developmental toxicity in animals or humans, it may reach the foetus and was found in milk. As a consequence, administration of propylene glycol to pregnant or lactating patients should be considered on a case by case basis.
- Medical monitoring is required in patients with impaired renal or hepatic functions because various adverse events attributed to propylene glycol have been reported such as renal dysfunction (acute tubular necrosis), acute renal failure and liver dysfunction.
- This medicine contains 0.9 mg of alcohol (ethanol) in each ml. The amount in 5ml dose of this medicine is equivalent to less than 0.1 ml beer or 0.05 ml wine. The small amount of alcohol in this medicine will not have any noticeable effects.
Hypoglycaemic agents: Tachycardia associated with hypoglycaemia may be modified by propranolol. Use of propranolol alongside hypoglycaemic therapy in diabetic patients should be with caution since it may prolong the hypoglycaemic response to insulin (see section 4.3 and 4.4).
Anti-arrhythmics: Class I anti-arrhythmic drugs (e.g. disopyramide and flecainide) may have a potentiating effect on atrial-conduction time and induce negative inotropic effect. Concomitant use with class III anti-arrhythmic drugs (e.g. amiodarone) increases the risk of bradycardia, AV block and myocardial depression.
Calcium Channel Blockers: Combined use of beta-adrenoceptor blocking drugs and calcium channel blockers with negative inotropic effects (eg, verapamil, diltiazem) can lead to an exaggeration of these effects particularly in patients with impaired ventricular function and/or SA or AV conduction abnormalities. This may result in severe hypotension, bradycardia and cardiac failure. Neither drug should be administered intravenously within 48 hours of discontinuing the other.
Dihydropyridines: Concomitant therapy with dihydropyridines e.g. nifedipine, may increase the risk of hypotension, and cardiac failure may occur in patients with latent cardiac insufficiency.
Digitalis Glycosides: These preparations in association with beta-adrenoceptor blocking drugs may increase atrio-ventricular conduction time.
Drugs with hypotensive effects: Dynamic interactions between propranolol and other drugs with hypotensive effects are to be expected. Reactions are sometimes severe and careful monitoring is advised in co-administration of propranolol with other drugs including ACE inhibitors, diuretics, angiotensin II receptor antagonists, vasodilator antihypertensives, diazoxide, adrenergic neurone blockers, alpha blockers, moxisylyte, moxonidine, nitrates and methyldopa.
Anaesthesia: Caution must be exercised when using anaesthetic agents with propranolol. The anaesthetist should be informed and the choice of anaesthetic should be the agent with as little negative inotropic activity as possible. Use of beta-adrenoceptor blocking drugs with anaesthetic drugs may result in attenuation of the reflex tachycardia and increase the risk of hypotension. Anaesthetic agents causing myocardial depression are best avoided.
Lidocaine / Bupivacaine: Administration of propranolol during infusion of lidocaine may increase the plasma concentration of lidocaine by approximately 30%. Patients already receiving propranolol tend to have higher lidocaine levels than controls. The combination should be avoided. There is an increased risk of bupivacaine toxicity when used with propranolol.
Neostigmine and other anticholinesterases: Propranolol reduces the efficacy of these compounds in treatment of myasthenia gravis.
Sympathomimetic Agents and Parenteral Adrenaline: Concomitant use of sympathomimetic agents e.g. adrenaline and dobutamine, may counteract the effect of beta-adrenoceptor blocking drugs. Caution should be taken in the parenteral administration of preparations containing adrenaline to people taking beta-adrenoceptor blocking drugs as, in rare cases, vasoconstriction, hypertension and bradycardia may result.
Muscle relaxants (e.g. baclofen): Concomitant use may result in a fall in blood pressure. Tizanidine may also result in bradycardia.
Antidepressants, anxiolytics and hypnotics: Plasma levels of propranolol can be increased by fluvoxamine. Anxiolytics, hypnotics and MAOIs when given with propranolol may have an enhanced hypotensive effect. Propranolol may increase plasma concentration of imipramine. Barbiturates may reduce the plasma concentration of propranolol.
Chlorpromazine: Concomitant administration with propranolol may result in an increase in plasma levels of both drugs. This may lead to an enhanced antipsychotic effect for chlorpromazine and an increased antihypertensive effect for propranolol.
Corticosteroids: Can antagonise the effects of beta-blockers.
Ergotamine: Caution should be exercised if ergotamine, dihydroergotamine or related compounds are given in combination with propranolol since vasospastic reactions have been reported in a few patients.
Prostaglandin Synthetase Inhibiting Drugs: Concomitant use of these e.g. ibuprofen or indomethacin, may decrease the hypotensive effects of propranolol.
Mefloquine: May lead to an increased risk of bradycardia.
Cimetidine, hydralazine: Concomitant use of cimetidine and hydralazine will increase the plasma level of propranolol.
Beta-blockers may exacerbate the rebound hypertension which can follow the withdrawal of clonidine. If the two drugs are co-administered, the betablocker should be withdrawn several days before discontinuing clonidine. If replacing clonidine by beta-blocker therapy, the introduction of betablockers should be delayed for several days after clonidine administration has stopped.
Alcohol (ethanol): Coadministration with alcohol may increase plasma propranolol levels (by enzyme inhibition), where as chronic use of alcohol may lower propranolol levels (by enzyme induction). Alcohol can have variable effects on the hypotensive action of propranolol.
Dopaminergics (e.g. Levodopa), Aldesleukin, Prostaglandins (alprostadil): May have an enhanced hypotensive effect when used concomitantly with propranolol.
Oestrogens: May antagonise the hypotensive effect of propranolol.
5HT1 agonists: Simultaneous administration of rizatriptan and propranolol can cause an increased rizatriptan AUC and Cmax by approximately 70-80%. The increased rizatriptan exposure is presumed to be caused by inhibition of first-passage metabolism of rizatriptan through inhibition of monoamine oxidase-A. If both drugs are to be used, a rizatriptan dose of 5 mg has been recommended.
Pharmacokinetic studies have shown that the following agents may interact with propranolol due to effects on enzyme systems in the liver which metabolise propranolol and these agents: quinidine, propafenone, rifampicin, theophylline, warfarin, thioridazine and dihydropyridine calcium channel blockers such as nifedipine, nisoldipine, nicardipine, isradipine and lacidipine. Owing to the fact that blood concentrations of either agent may be affected, dosage adjustments may be needed according to clinical judgement. (See also the interaction above concerning the concomitant therapy with dihydropyridine calcium channel blockers).
As with all drugs, propranolol should not be given in pregnancy unless absolutely essential. There is no evidence of teratogenicity with propranolol. However, beta adrenoceptor blocking agents reduce placenta perfusion, which may result in intra-uterine foetal death, immature and premature deliveries. In addition, adverse effects (especially hypoglycaemia and bradycardia in the neonate and bradycardia in the foetus) may occur. There is an increased risk of cardiac and pulmonary complications in the neonate in the post-natal period.
Most beta-adrenoceptor blocking drugs particularly lipophilic compounds, will pass into breast milk although to a variable extent. Breast feeding is therefore not recommended following administration of these compounds.
Use is unlikely to result in any impairment of the ability of patients to drive or operate machinery. However, it should be taken into account that occasionally dizziness or fatigue may occur.
Propranolol is usually well tolerated, however, listed below are the side effects that may occur:
The following undesired events, listed by body system, have been reported.
The following definitions of frequencies are used:
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).
≥1/100 to <1/10
≥1/1,000 to <1/100
≥1/10,000 to <1/1,000)
(frequency cannot be estimated from the available data
Blood and lymphatic system disorders:
Hypoglycaemia in neonates, infants, children, elderly patients, patients on haemodialysis, patients on concomitant antidiabetic therapy, patients with prolonged fasting and patients with chronic liver disease has been reported, seizure linked to hypoglycaemia
Nervous system disorders:
Sleep disturbances, nightmares
Confusion, mood changes, psychoses, hallucinations memory loss, paraesthesia
Isolated reports of myasthenia gravis like syndrome or exacerbation of myasthenia gravis have been reported
Dry eyes, visual disturbances
Heart failure deterioration, precipitation of heart block, congestive cardiac failure
Cold extremities, Raynaud's phenomenon
Exacerbation of intermittent claudication, postural hypotension which may be associated with syncope
Respiratory, thoracic and mediastinal disorders:
Bronchospasm may occur in patients with bronchial asthma or a history of asthmatic complaints, sometimes with fatal outcome
Gastrointestinal disturbance, such as nausea, vomiting, diarrhoea
Skin and subcutaneous tissue disorders:
Purpura, alopecia, psoriasiform skin reactions, exacerbation of psoriasis, skin rashes
General disorders and administration site conditions:
Fatigue and/or Lassitude (often transient)
An increase in ANA (antinuclear antibodies), although the clinical relevance of this has not been established
If these effects occur, thought should be given to withdrawing the drug. However, it should be withdrawn gradually.
Bradycardia and hypotension are usually a sign of overdosage but may be rarely linked to intolerance. If this occurs the drug should be withdrawn and overdosage treatment initiated.
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. Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
The symptoms of overdosage may include bradycardia, hypotension, acute cardiac insufficiency and bronchospasm.
General treatment should include: close supervision, treatment in an intensive care ward, the use of gastric lavage, activated charcoal and a laxative to prevent absorption of any drug still present in the gastrointestinal tract, the use of plasma or plasma substitutes to treat hypotension and shock.
Excessive bradycardia can be countered with atropine 1–2mg intravenously and/or a cardiac pacemaker. If necessary, this may be followed by a bolus dose of glucagon 10mg intravenously. If required, this may be repeated or followed by an intravenous infusion of glucagon 1–10mg/hour depending on response. If no response to glucagon occurs or if glucagon is unavailable, a beta-adrenoceptor stimulant such as dobutamine 2.5 to 10 micrograms/Kg/minute by intravenous infusion may be given. Dobutamine, because of its positive inotropic effect could also be used to treat hypotension and acute cardiac insufficiency. It is likely that these doses would be inadequate to reverse the cardiac effects of beta-blockade if a large overdose has been taken. The dose of dobutamine should therefore be increased if necessary to achieve the required response according to the clinical condition of the patient.
Pharmacotherapeutic group: Beta blocking agents, non-selective, ATC code: C07AA05
Propranolol is a competitive antagonist at both beta1 and beta2-adrenoceptors.
It has no agonist activity at the beta-adrenoceptor, but has membrane stabilising activity at concentrations exceeding 1-3mg/litre, though such concentrations are rarely achieved during oral therapy. Competitive beta-adrenoceptor blockade has been demonstrated in man by a parallel shift to the right in the dose-heart rate response curve to beta-agonists such as isoprenaline.
Propranolol, as with other beta-adrenoceptor blocking drugs, has negative inotropic effects, and is therefore contra-indicated in uncontrolled heart failure.
Propranolol is a racemic mixture and the active form is the S(–) isomer. With the exception of inhibition of the conversion of thyroxine to triiodothyronine it is unlikely that any additional ancillary properties possessed by R(+) propranolol, in comparison with the racemic mixture will give rise to different therapeutic effects.
Propranolol is effective and well tolerated in most ethnic populations, although the response may be less in black patients.
Following intravenous administration, the plasma half-life of propranolol is about 2 hours and the ratio of metabolites to parent drug in the blood is lower than after oral administration. In particular, 4-hydroxypropranolol is not present after intravenous administration.
Propranolol is completely absorbed after oral administration and peak plasma concentrations occur 1–2 hours after dosing in fasting patients. The liver removes up to 90% of an oral dose with an elimination half-life of 3 to 6 hours. Propranolol is widely and rapidly distributed throughout the body with highest levels occurring in the lungs, liver, kidney, brain and heart.
Propranolol is highly protein bound (80–95%).
Propranolol is a drug on which extensive clinical experience has been obtained. Relevant information for the prescriber is provided elsewhere in the Summary of Product Characteristics.
Citric acid monohydrate (E330), methyl parahydroxybenzoate (E218), propyl parahydroxybenzoate (E216), propylene glycol (E1520), liquid maltitol (E965), orange/tangerine flavour (including ethanol (0.12%v/v) and butylhydroxyanisol (E320)) and purified water.
24 months unopened
3 months opened.
Do not store above 25°C. Do not refrigerate or freeze.
Amber (Type III) glass bottles
HDPE, EPE wadded, tamper evident, child resistant closure.
Rosemont Pharmaceuticals Ltd,
Yorkdale Industrial Park,
Date of first authorisation: 11th December 2000,
Date of renewal: 30th August 2006
11. LEGAL CATEGORY
Rosemont House, Yorkdale Industrial Park, Braithwaite Street, Leeds, Yorkshire, LS11 9XE
+44 (0)113 244 1400
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