Zuellig Pharma
Full Prescribing Info
Propranolol hydrochloride.
Tablets containing 10 mg or 40 mg Propranolol Hydrochloride Ph. Eur.
Pharmacology: Pharmacodynamics: Propranolol is a competitive antagonist at both the beta-1 and beta-2 adrenoceptors. It has no agonist activity at the beta-adrenoceptor, but has membrane stabilising activity at concentrations exceeding 1-3 mg/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-blockers, has negative inotropic effects, and is therefore contraindicated in uncontrolled heart failure (see Precautions).
Propranolol is a racemic mixture and the active form is the S(-) isomer, of propranolol. 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.
Pharmacokinetics: 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%).
i) Control of hypertension
ii) Management of angina pectoris
iii) Long term prophylaxis after recovery from acute myocardial infarction
iv) Control of cardiac arrhythmias
v) Prophylaxis of migraine
vi) Management of essential tremor
vii) Control of anxiety and anxiety tachycardia
viii) Adjunctive management of thyrotoxicosis
ix) Management of hypertrophic obstructive cardiomyopathy
x) Management of phaeochromocytoma (Inderal should only be started in the presence of effective alpha blockade).
Dosage/Direction for Use
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.
Adults: Hypertension: A starting dose of 80 mg twice a day may be increased at weekly intervals according to response. The usual dose range is 160-320 mg per day and the maximum daily dose must not exceed 640 mg per day (see table). With concurrent diuretic or other antihypertensive drugs a further reduction of blood pressure is obtained.
Angina, anxiety, migraine and essential tremor: A starting dose of 40 mg two or three times daily may be increased by the same amount at weekly intervals according to patient response. An adequate response in anxiety, migraine and essential tremor is usually seen in the range.
80-160 mg/day, and in angina in the range 120-240 mg/day. A maximum daily dose of 240 mg for migraine and 480 mg for angina must not be exceeded (see table).
Arrhythmias, anxiety tachycardia, hypertrophic obstructive cardiomyopathy and thyrotoxicosis: A dosage range of 10-40 mg three or four times a day usually achieves the required response. A maximum daily dose of 240 mg for arrhythmias must not be exceeded. (See table.)
Post-myocardial infarction: Treatment should start between days 5 and 21 after myocardial infarction, with an initial dose of 40 mg four times a day for 2 or 3 days. In order to improve compliance the total daily dosage may thereafter be given as 80 mg twice a day (see table).
Phaeochromocytoma: (Inderal is to be used only in the presence of effective alpha-blockade). Preoperative: 60 mg daily for three days is recommended. Non-operable malignant cases: 30 mg daily (see table).

Click on icon to see table/diagram/image

Elderly: Evidence concerning the relation between blood level and age is conflicting. With regard to the elderly, the optimum dose should be individually determined according to clinical response.
Children: Dosage should be individually determined and the following is only a guide: Arrhythmias, phaeochromocytoma, thyrotoxicosis: 0.25 - 0.5 mg/kg three or four times daily as required.
Migraine: Under the age of 12: 20 mg two or three times daily. Over the age of 12: the adult dose.
Propranolol is known to cause severe toxicity when used in overdose. Patients should be informed of the signs of overdose and advised to seek urgent medical assistance if an overdose of propranolol has been taken.
Clinical features: Cardiac: Bradycardia, hypotension, and cardiogenic shock may develop. QRS complex prolongation, ventricular tachycardia, first to third degree AV block, ventricular fibrillation or asystole may also occur. Development of cardiovascular complications is more likely if other cardioactive drugs, especially calcium channel blockers, digoxin, cyclic antidepressants or neuroleptics have also been ingested.
CNS: Drowsiness, seizures, and in severe cases coma may occur.
Other features: Bronchospasm, hyperkalaemia and occasionally CNS-mediated respiratory depression may occur.
Management: 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 10 mg intravenously. If required, this may be repeated or followed by an intravenous infusion of glucagon 1-10 mg/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.
Inderal must not be used if there is a history of bronchial asthma or bronchospasm.
Bronchospasm can usually be reversed by beta-2-agonist bronchodilators such as salbutamol. Large doses of the beta-2-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 2 mg given intravenously) has also been reported to produce a bronchodilator effect in asthmatic patients. Oxygen or artificial ventilation may be required in severe cases.
Inderal as with other beta-blockers must not be used in patients with any of the following: known hypersensitivity to the substance; bradycardia; cardiogenic shock; hypotension; metabolic acidosis; after prolonged fasting; severe peripheral arterial circulatory disturbances; second or third degree heart block; sick sinus syndrome; untreated (with an alpha adrenoceptor antagonist) phaeochromocytoma; uncontrolled heart failure; Prinzmetal's angina.
Inderal 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.
Special Precautions
Inderal as with other beta-blockers: although contraindicated in uncontrolled heart failure (see Contraindications), may be used in patients whose signs of heart failure have been controlled. Caution must be exercised in patients whose cardiac reserve is poor.
Although contraindicated in severe peripheral arterial circulatory disturbances (see Contraindications), may also aggravate less severe peripheral arterial circulatory disturbances.
Due to its negative effect on conduction time, caution must be exercised if it is given to patients with first degree heart block.
May block/modify the signs and symptoms of the hypoglycaemia (especially tachycardia). Inderal 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 patient suffering from overdose. Severe hypoglycemia associated with Inderal has rarely presented with seizures and/or coma in isolated patients. Caution must be exercised in the concurrent use of Inderal and hypoglycaemic therapy in diabetic patients. Inderal may prolong the hypoglycaemic response to insulin.
May mask the signs of thyrotoxicosis.
Will reduce heart rate, as a result of its pharmacological action. In the rare instances when a treated patient develops symptoms which may be attributable to a slow heart rate, the dose may be reduced.
Should not be discontinued abruptly in patients suffering from ischaemic heart disease. Either the equivalent dosage of another beta-blocker may be substituted or the withdrawal of Inderal should be gradual.
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 adrenalin used to treat the allergic reactions.
Inderal must be used with caution in patients with decompensated cirrhosis.
In patients with significant hepatic or renal impairment, care should be taken 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.
Effect on Ability to Drive or Operate Machinery: 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.
Use In Pregnancy & Lactation
Pregnancy: As with all drugs, Inderal should not be given during pregnancy unless its use is essential. There is no evidence of teratogenicity with Inderal. However beta-blockers reduce placental 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.
Lactation: Most beta-blockers, particularly lipophilic compounds, will pass into breast milk although to a variable extent. Breast-feeding is therefore not recommended following administration of these compounds.
Adverse Reactions
Inderal is usually well tolerated. In clinical studies the possible adverse reactions reported are usually attributable to the pharmacological actions of propranolol.
The following possible adverse reactions, listed by body system, have been reported.
Common (1-9.9%): General: Fatigue and/or lassitude (often transient).
Cardiovascular: Bradycardia, cold extremities, Raynaud's phenomenon.
CNS: Sleep disturbances, nightmares.
Uncommon (0.1-0.9%): GI: Gastrointestinal disturbance, such as nausea, vomiting, diarrhoea.
Rare (0.01-0.09%): General: Dizziness.
Blood: Thrombocytopaenia.
Cardiovascular: Heart failure deterioration, precipitation of heart block, postural hypotension, which may be associated with syncope, exacerbation of intermittent claudication.
CNS: Hallucinations, psychoses, mood changes, confusion, memory loss.
Skin: Purpura, alopecia, psoriasiform skin reactions, exacerbation of psoriasis, skin rashes.
Neurological: Paraesthesia.
Eyes: Dry eyes, visual disturbances.
Respiratory: Bronchospasm may occur in patients with bronchial asthma or a history of asthmatic complaints, sometimes with fatal outcome.
Very rare (<0.01%): Endocrine system: 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.
Investigations: an increase in ANA (Antinuclear Antibodies) has been observed, however the clinical relevance of this is not clear.
Nervous system: Isolated reports of myasthenia gravis like syndrome or exacerbation of myasthenia gravis have been reported.
Discontinuance of the drug should be considered if, according to clinical judgement, the well-being of the patient is adversely affected by any of the previously mentioned reactions. Cessation of therapy with a beta-blocker should be gradual. In the rare event of intolerance, manifested as bradycardia and hypotension, the drug should be withdrawn and, if necessary, treatment for overdosage instituted.
Drug Interactions
Inderal modifies the tachycardia of hypoglycaemia. Caution must be exercised in the concurrent use of Inderal and hypoglycaemic therapy in diabetic patients. Inderal may prolong the hypoglycaemic response to insulin (see Contraindications and Precautions).
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.
Class I anti-arrhythmic drugs (e.g. disopyramide) and amiodarone may have potentiating effect on atrial-conduction time and induce negative inotropic effect.
Digitalis glycosides in association with beta-blockers may increase atrioventricular conduction time.
Combined use of beta-blockers and calcium channel blockers with negative inotropic effects (e.g. 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 the beta-blocker nor the calcium channel blocker should be administered intravenously within 48 hours of discontinuing the other.
Concomitant therapy with dihydropyridine calcium channel blockers e.g. nifedipine, may increase the risk of hypotension and cardiac failure may occur in patients with latent cardiac insufficiency.
Concomitant use of sympathomimetic agents, eg adrenalin, may counteract the effect of beta-blockers. Caution must be exercised in the parenteral administration of preparations containing adrenalin to patients taking beta-blockers as, in rare cases, vasoconstriction, hypertension and bradycardia may result.
Administration of Inderal during infusion of lignocaine may increase the plasma concentration of lignocaine by approximately 30%. Patients already receiving Inderal tend to have higher lignocaine levels than controls. The combination should be avoided.
Concomitant use of cimetidine or hydralazine increases, and concomitant use of alcohol may increase the plasma levels of propranolol.
Beta-blockers may exacerbate the rebound hypertension which can follow the withdrawal of clonidine. If the two drugs are co-administered, the beta-blocker should be withdrawn several days before discontinuing clonidine. If replacing clonidine by beta-blocker therapy, the introduction of beta-blockers should be delayed for several days after clonidine administration has stopped.
Caution must be exercised if ergotamine, dihydroergotamine or related compounds are given in combination with Inderal since vasospastic reactions have been reported in a few patients.
Concomitant use of prostaglandin synthetase inhibiting drugs e.g. ibuprofen and indomethacin, may decrease the hypotensive effects of Inderal.
Concomitant administration of Inderal and chlorpromazine 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 Inderal.
Caution must be exercised when using anaesthetic agents with Inderal. The anaesthetist should be informed and the choice of anaesthetic should be an agent with as little negative inotropic activity as possible. Use of beta-blockers 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.
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 previously mentioned concerning the concomitant therapy with dihydropyridine calcium channel blockers).
Do not store above 30°C. Protect from light and moisture.
MIMS Class
ATC Classification
C07AA05 - propranolol ; Belongs to the class of non-selective beta-blocking agents. Used in the treatment of cardiovascular diseases.
Inderal tab 10 mg
Inderal tab 40 mg
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