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Esmolol 10 mg/ml – patient leaflet, side effects, dosage

Last updated: · Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) Details

Medicine strength:
10 mg / ml
Contains active substance:
ATC code:

Patient leaflet - Esmolol 10 mg / ml solution for injection

1. WHAT ESMOLOL IS AND WHAT IT IS USED FOR

Esmolol contains a medicine called esmolol. It belongs to a group of medicines called ‘beta-blockers’. It works by controlling the rate and force of your heartbeat. It can also help to reduce your blood pressure.

It is used to treat:

  • Heartbeat problems, when your heart beats too fast.
  • Heartbeat problems and an increase in your blood pressure if this

    happens during or straight after an operation.

2. WHAT YOU NEED TO KNOW BEFORE YOU ARE GIVEN ESMOLOL

Your doctor will not give you Esmolol if:

  • You are allergic to esmolol, to other beta-blocker medicines, or any of the

    other ingredients of this medicine (listed in section 6). The signs of an allergic reaction include shortness of breath, wheezing, rash, itching or swelling of your face and lips.

  • You have a very slow heartbeat (less than 50 beats per minute).
  • You have a fast or alternating fast and slow heartbeat.
  • You have something called “severe heart block”. Heart block is a problem

    with the electrical messages that control your heartbeat.

  • You have low blood pressure.
  • You have a problem with the blood supply to your heart.
  • You have serious heart failure symptoms.
  • You are receiving or have recently received verapamil. You must not be

    given Esmolol within 48 hours of when you stop receiving verapamil.

  • You have a gland disease called phaeochromocytoma which has not been

    treated. Phaeochromocytoma arises from the adrenal gland and may cause a sudden increase in blood pressure, severe headache, sweating and increased heartbeat.

  • You have increased blood pressure in the lungs (pulmonary hypertension).
  • You have asthma symptoms that are worsening rapidly.
  • You have increased levels of acids in your body (metabolic acidosis).

You will not be given Esmolol if any of the above applies to you. If you are not sure if you have any of these conditions, talk to your doctor or nurse before having Esmolol.

Warnings and precautions

Talk to your doctor or nurse before being given Esmolol.

Your doctor will take special care with this medicine if:

  • You are being treated for certain heart rhythm disorders called

    supraventricular arrhythmias and you:

    • Have other heart problems or
    • Are taking other heart medicines

Use of Esmolol in this way can lead to severe reactions which may be fatal including:

  • Loss of consciousness
  • Shock (when your heart does not pump enough blood)
  • Heart attack (cardiac arrest)
  • You develop low blood pressure (hypotension). The signs of this may be

    feeling dizzy or light headed, especially when standing up. Low blood pressure usually gets better within 30 minutes of the end of your Esmolol treatment.

  • You have a low heart rate before treatment.
  • Your heart rate decreases to less than 50 to 55 beats per minute. If this

    happens your doctor may give you a lower dose or stop treatment with Esmolol.

  • You have heart failure.
  • You have problems with the electrical messages that control your

    heartbeat (heart block).

  • You have a gland disease called phaeochromocytoma which has been

    treated with medicines called alpha-receptor blockers.

  • You are being treated for high blood pressure (hypertension) which has

    been caused by low body temperature (hypothermia).

  • You have narrowing of your airways or wheezing, such as with asthma.
  • You have diabetes or low blood sugar. Esmolol can increase the effects of

    your diabetes medicines.

  • You develop skin problems. These can be caused by the solution leaking

    around the site of the injection. If this happens your doctor will use a different vein for your injection.

  • You have a particular type of angina (chest pain) called ‘Prinzmetal’s

    angina’.

  • You have low blood volume (with low blood pressure). You could develop

    circulatory collapse more easily.

  • You have circulation problems, such as paleness of your fingers

    (Raynaud’s disease) or aching, tired and sometimes burning pains in your legs.

    • You have kidney problems. If you have kidney disease or you need kidney dialysis you could develop high blood potassium levels (hyperkalemia). This can cause serious heart problems.
    • You have any allergies or are at risk of anaphylactic reactions (severe allergic reactions). Esmolol can make allergies more severe and more difficult to treat.
    • You or any of your family have a history of psoriasis (where your skin produces scaly patches).
    • You have a disease called hyperthyroidism (an overactive thyroid gland).

Changing the dose is not usually necessary if you have liver problems.

If any of the above apply to you (or you are not sure), talk to your doctor or nurse before being given this medicine. You may need to be checked carefully and your treatment may be changed.

Other medicines and Esmolol

Tell your doctor if you are using, have recently used or might use any other medicines. This includes medicines that you have obtained yourself, without a prescription, including herbal medicines and natural products. Your doctor will check that any other medicines you are taking will not alter the way that Esmolol works.

In particular, tell your doctor or nurse if you are taking any of the following:

  • Medicines that can lower the blood pressure or slow the heart rate.
  • Medicines used to treat heart rhythm problems or chest pain (angina) such as verapamil and diltiazem. You should not receive Esmolol within 48 hours of stopping verapamil.
  • Nifedipine, which is used to treat chest pain (angina), high blood pressure and Raynaud’s disease.
  • Medicines used to treat heart rhythm problems (such as quinidine, disopyramide, amiodarone) and heart failure (such as digoxin, digitoxin, digitalis).
  • Medicines used to treat diabetes, including insulin and medicines taken by mouth.
  • Medicines known as ganglion blocking agents (such as trimetaphan).
  • Medicines used as pain killers, such as non-steroidal anti-inflammatory drugs known as NSAIDs.
  • Floctafenine, which is a pain killer.
  • Amisulpride, a medicine that is used to treat mental problems.
  • ‘Tricyclic’ antidepressant medicines (such as imipramine and amitriptyline)

    or any other drugs for mental health problems.

  • Barbiturates (such as phenobarbital, used to treat epilepsy) or

    phenothiazines (such as chlorpromazine, used to treat mental disorders).

  • Clozapine which is used to treat mental disorders.
  • Epinephrine, which is used to treat allergic reactions.
  • Medicines used to treat asthma.
  • Medicines used to treat colds or a blocked nose, called ‘nasal

    decongestants’.

  • Reserpine, which is used to treat high blood pressure.
  • Clonidine, which is used to treat high blood pressure and migraine.
  • Moxonidine, which is used to treat high blood pressure.
  • Ergot derivates, medicines mainly used to treat Parkinson's disease.
  • Warfarin, which is used to thin your blood.
  • Morphine, which is a strong pain killer.
  • Suxamethonium chloride (also known as succinylcholine or scoline) or mivacurium, which are used to relax your muscles, usually during an operation. Your doctor will also take special care when using Esmolol during operations, when you will be having anaesthetics and other treatments.

If you are not sure if any of the above applies to you talk to your doctor, nurse or pharmacist before having Esmolol.

Tests you may have while Esmolol is used

The use of medicines such as Esmolol over a long period of time can cause a reduction in the force of your heartbeat.

Since Esmolol is only used for a limited time, this is unlikely to happen to you. During treatment you will be carefully monitored and Esmolol treatment will be reduced or stopped if the force of your heartbeat is reduced.

Your doctor will also check your blood pressure while you are being treated with Esmolol.

Pregnancy and breast-feeding

Ask your doctor or pharmacist for advice before taking any medicine.

You should not be given Esmolol if you are pregnant, or if you think you may be pregnant.

Tell your doctor if you are breast-feeding. Esmolol may pass into breast milk, so you should not be given Esmolol if you are breast-feeding.

Esmolol contains sodium

This medicinal product contains less than 1 mmol sodium (23 mg) per vial, i.e. essentially ‘sodium-free’.

3. HOW YOU WILL BE GIVEN ESMOLOL

Your doctor will decide how much of the medicine you will need and for how long it will be given to you. Esmolol will not normally be given for longer than 24 hours.

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Esmolol 10 mg/ml

Solution for injection

esmolol hydrochloride

The following information is intended for medical or healthcare professionals only:

Posology and method of administration

Esmolol is a ready-to-use 10 mg/ml solution recommended for intravenous administration. This dosage form is used to administer the appropriate Esmolol loading dose or bolus dose by hand held syringe.

Posology is summarised in the following tables.

Table 1: Volume of Esmolol 10 mg/ml required for an INITIAL LOADING DOSE of 500 mcg/kg/minute

Table 2: Volume of Esmolol 10 mg/ml required to provide MAINTENANCE DOSES at infusion rates between 12.5 and 300 mcg/kg/minute

Patient weight (kg)

Volume (ml)

405060708090100110120
22.533.544.555.56
Infusion Dose Rate

Patient weight (kg)

12.5

mcg/kg/min

25

mcg/kg/min

50

mcg/kg/min

100

mcg/kg/min

150

mcg/kg/min

200

mcg/kg/min

300

mcg/kg/min

Amount to administer per hour to achieve the dose rate (ml / hr)

40

50

60

70

80

90

100

110

120

3 ml/hr6 ml/hr12 ml/hr24 ml/hr36 ml/hr48 ml/hr72 ml/hr
3.75 ml/hr7.5 ml/hr15 ml/hr30 ml/hr45 ml/hr60 ml/hr90 ml/hr
4.5 ml/hr9 ml/hr18 ml/hr36 ml/hr54 ml/hr72 ml/hr108 ml/hr
5.25 ml/hr10.5 ml/hr21 ml/hr42 ml/hr63 ml/hr84 ml/hr126 ml/hr
6 ml/hr12 ml/hr24 ml/hr48 ml/hr72 ml/hr96 ml/hr144 ml/hr
6.75 ml/hr13.5 ml/hr27 ml/hr54 ml/hr81 ml/hr108 ml/hr162 ml/hr
7.5 ml/hr15 ml/hr30 ml/hr60 ml/hr90 ml/hr120 ml/hr180 ml/hr
8.25 ml/hr16.5 ml/hr33 ml/hr66 ml/hr99 ml/hr132 ml/hr198 ml/hr
9 ml/hr18 ml/hr36 ml/hr72 ml/hr108 ml/hr144 ml/hr216 ml/hr

How Esmolol is given

Esmolol is ready to use. You will be given Esmolol by a slow injection (infusion) through a needle inserted into a vein in your arm. Esmolol must not be mixed with sodium bicarbonate or other medicinal products.

  • The treatment is given in two stages:

    • Stage one: a large dose is given over one minute. This increases the levels in your blood quickly.
    • Stage two: a smaller dose is then given over four minutes.
    • Stage one and two may then be repeated and adjusted according to your heart’s response. As soon as an improvement has happened, stage one (the large dose) will be stopped and stage two (the small dose) will be reduced as necessary.
    • After reaching a stable condition, you may be given another heart drug, while your dose of Esmolol is gradually reduced.
  • If your heart rate or blood pressure increases during an operation or

    straight after recovering from it, you will be given larger doses of Esmolol for a short time.

Use in elderly

Your doctor will start your treatment with a lower dose.

Use in children

Children up to the age of 18 years should not receive Esmolol.

If you have too much Esmolol

As you are being given Esmolol by a trained and qualified person, it is unlikely that you will have too much. However, if this happens the doctor will stop Esmolol and give you additional treatment, if necessary.

If you think that a dose of Esmolol has been forgotten

As you are being given Esmolol by a trained and qualified person, it is unlikely that you will miss a dose. However, if you think that you have missed a dose, talk to your doctor, nurse or pharmacist as soon as possible.

If you stop having Esmolol

Suddenly stopping Esmolol may cause symptoms of rapid heartbeat (tachycardia) and high blood pressure (hypertension) to return. To avoid this your doctor should stop your treatment gradually. If you are known to have coronary artery disease (this may be associated with a history of angina or heart attack) your doctor will take special care when stopping treatment with Esmolol.

If you have any further questions on the use of this medicine, ask your doctor or nurse.

4. POSSIBLE SIDE EFFECTS

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Most side effects disappear within 30 minutes of stopping treatment with Esmolol.

Tell your doctor or nurse straight away if you notice any of the following side effects, which can be serious. The infusion may also need to be stopped.

The following side effects have been reported with Esmolol:

Very common (may affect more than 1 in 10 people)

  • Fall in blood pressure. This can be rapidly corrected by reducing the dose

    of Esmolol or stopping the treatment. Your blood pressure will be measured often during treatment.

  • Excessive sweating

Common (may affect less than 1 in 10 people)

  • Loss of appetite
  • Feeling anxious or depressed
  • Dizziness
  • Feeling sleepy
  • Headache
  • Tingling or ‘pins and needles’.
  • Difficulty concentrating
  • Feeling confused or agitated
  • Feeling or being sick (nausea and vomiting)
  • Feeling weak
  • Feeling tired (fatigue)
  • Irritation and hardening of your skin where Esmolol was injected.

Uncommon (may affect less than 1 in 100 people)

  • Abnormal thoughts
  • Sudden loss of consciousness
  • Feeling faint or fainting
  • Fits (seizures or convulsions)
  • Problems with speech
  • Problems with eyesight
  • Slow heart rate
  • Problems with the electrical messages that control your heartbeat
  • Increased pressure in the arteries of the lungs
  • Inability of the heart to pump enough blood (heart failure)
  • A disruption in the rhythm of the heart sometimes known as palpitations

    (ventricular extrasystoles)

  • A heartbeat disorder (nodal rhythm)
  • Chest discomfort caused by poor blood flow through the blood vessels of

    the heart muscle (angina pectoris)

  • Poor circulation in your arms or legs
  • Looking pale or flushed
  • Fluid on your lungs
  • Shortness of breath or tightness of the chest making it difficult to breathe
  • Wheezing

Perioperative tachycardia and hypertension

For perioperative tachycardia and hypertension the dosing regimen may vary as follows:

For intraoperative treatment - during anaesthesia when immediate control is required:

  • A bolus injection of 80 mg is given over 15 to 30 seconds followed by a

    150 micrograms/kg/minute infusion. Titrate the infusion rate as required up to 300 micrograms/kg/minute. The volume of infusion required for different patient weights is provided in Table 2.

Upon awakening from anaesthesia

  • An infusion of 500 micrograms/kg/minute is given for 4 minutes followed

    by a 300 micrograms/kg/minute infusion. The volume of infusion required for different patient weights is provided in Table 2.

For post-operative situations when time for titration is available

  • A loading dose of 500 micrograms/kg/minute is given over 1 minute

    before each titration step to produce a rapid onset of action. Use titration steps of 50, 100, 150, 200, 250 and 300 micrograms/kg/minute given over 4 minutes and stopping at the desired therapeutic effect. The volume of infusion required for different patient weights is provided in Table 2.

    Incompatibilities

    In the absence of compatibility studies, this medicinal product must not be mixed with other medicinal products or sodium bicarbonate solutions.

    Special precautions for disposal and other handling

    For single use only.

    Avoid contact with alkali.

    The solution should be visually inspected for particulate matter and discolouration prior to administration. Only a clear and colourless or slightly coloured solution should be used. Any unused medicinal product or waste material should be disposed of in accordance with local requirements.

    • Blocked nose
    • Abnormal rattling/crackling sounds when breathing
    • Changes in your sense of taste
    • Indigestion
    • Constipation
    • Dry mouth
    • Pain in your stomach area
    • Discoloured skin
    • Reddening of the skin
    • Pain in your muscles or tendons, including around the shoulder blades and ribs
    • Problems passing urine (urinary retention)
    • Feeling cold or high temperature (fever)
    • Pain and swelling (oedema) of your vein where Esmolol was injected.
    • Burning feeling or bruising at the site of injection.

Very rare (may affect less than 1 in 10,000 people)

  • Severe reduction in heart rate (sinus arrest)
  • No electrical activity in the heart (asystole)
  • Tender blood vessels with an area of hot red skin (thrombophlebitis)
  • Dead skin caused by the solution leaking around the site of the injection.

Not known (the number of people affected is unknown)

  • Increased levels of potassium in the blood (hyperkalemia)
  • Increased levels of acids in your body (metabolic acidosis)
  • Increased rate of contraction of the heart (accelerated idioventricular rhythm)
  • Spasm of the artery in the heart
  • Failure of the normal circulation of the blood (cardiac arrest)
  • Psoriasis (where your skin produces scaly patches)
  • Swelling of the skin of the face, limbs, tongue or throat (angioedema)
  • Hives (urticaria)
  • Inflammation of a vein or blistering at the site of infusion.

Reporting of side effects

If you get any side effects, talk to your doctor or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly 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. By reporting side effects you can help provide more information on the safety of this medicine.

5. HOW TO STORE ESMOLOL

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the label and carton after EXP.

Do not store above 25oC.

Chemical and physical in-use stability has been demonstrated for 24 hours at 2 to 8°C.

Keep the vial in the outer carton in order to protect from light.

6. CONTENTS OF THE PACK AND OTHER INFORMATION

What Esmolol contains

  • The active substance is esmolol hydrochloride.
  • The other ingredients are sodium acetate trihydrate, glacial acetic acid, sodium hydroxide and/or hydrochloric acid for pH adjustment and water for injections.

Each ml of solution contains 10 mg esmolol hydrochloride, equivalent to 8.9 mg esmolol.

Each 10 ml vial of solution contains 100 mg esmolol hydrochloride, equivalent to 89 mg esmolol.

What Esmolol looks like and contents of the pack

Esmolol is a clear colourless to light yellow solution packed in 10 ml, type I amber glass vials, packed in cardboard cartons.

Pack size: 10 vials.

Marketing Authorisation Holder and Manufacturer

Hikma Farmacêutica (Portugal) S.A.

Estrada do Rio da Mó, nº8, 8A e 8B

Fervença

2705-906 Terrugem SNT

Portugal

This leaflet was last revised in November 2024.

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About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 15413/0055

Last revision stated in the text: November 2024 · MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Facts about Esmolol 10 mg / ml solution for injection

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Esmolol
Strength 10 mg / ml
Pharmaceutical form Solution for injection
How is it taken Intravenous
Pack sizes 10 vial
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Drug group (ATC)
  1. C Cardiovascular system drugs
    1. C07 Beta-Adrenergic Blocking Agents
      1. C07A Beta blocking agents
        1. C07AB Beta blocking agents, selective
          1. C07AB09 esmolol
Marketing authorisation PL 15413/0055
Codes GTIN 5061024110682 · BNF 02040000

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.1.0 of 12 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.