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Phentolamine Mesilate 10 mg/ml solution for injection – 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:

Patient leaflet - Phentolamine Mesilate 10 mg/ml solution for injection

1. What Phentolamine solution for injection is and what it is used for

The active substance in Phentolamine mesilate 10 mg/ml solution for injection (called Phentolamine solution for injection in this leaflet) is phentolamine. It belongs to a group of medicines called alpha blockers. These medicines lower high blood pressure by relaxing blood vessels.

Phentolamine solution for injection can be used in the following cases:

  • For the treatment of high blood pressure caused by a tumour of certain cells in the adrenal medulla (pheochromocytoma) before and during the surgery.
  • As a test to diagnose

    pheochromocytoma, if other tests are not available.

Ask your doctor if you are not sure why Phentolamine solution for injection is going to be used for you.

2. What you need to know before you use Phentolamine solution for injection

Do not take Phentolamine solution for injection:

  • if you are allergic to phentolamine mesilate or any of the other ingredients of this medicine (listed in section 6).
  • if you are hypersensitive to sulphite.
  • if you have low blood pressure.
  • if you are having a heart attack or if you have had a heart attack in the past.
  • if your heart does not function properly and if you have chest tightness or any other signs of disease of the blood vessels around the heart.

Warnings and precautions

Talk to your doctor or pharmacist before using this medicine:

  • if you have fast or irregular heartbeats.
  • if you have heartburn, abdominal pain, nausea or vomiting.
  • if you have darker coloured stools or blood in your stools.
  • if you have kidney impairment.

Children and adolescents

This medicine can be used in children and adolescents up to 18 years of age.

Other medicines and Phentolamine solution for injection

Tell your doctor or pharmacist if you are using, have recently used or might use any other medicines. This applies especially to other blood

pressure-lowering medicines and medicines for the treatment of certain mental and emotional disorders.

Pregnancy and breast-feeding

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine. Your doctor will inform you about the benefits and risks and decide whether Phentolamine solution for injection can be used for you. Also talk to your doctor if want to breast-feed. Phentolamine solution for injection is not advised for use in breast-feeding women.

Driving and using machines

Phentolamine solution for injection may cause dizziness or other side effects. Do not drive or use machines if this happens to you. If so, contact your doctor.

Phentolamine solution for injection contains sodium metabisulphite.

In rare cases, sodium metabisulphite can cause severe hypersensitivity reactions and shortness of breath due to spasm of the muscles of the airways (bronchospasm).

This medicine contains less than 1 mmol sodium (23 mg) per each 1 ml ampoule, that is to say essentially ‘sodium-free’.

3. How to take Phentolamine solution for injection

This medicine is for use in hospitals and will be given by a doctor or nurse as an injection.

Your doctor will determine the dose.

Duration of the treatment

Your doctor will decide the duration of the treatment.

If you are given more Phentolamine solution for injection than you should

This medicine is given to you by your doctor or nurse. It is unlikely that you will be given too much. Your doctor will carefully work out how much you should be given.

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.

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

  • fast heart rate (tachycardia)
  • low blood pressure when sitting or standing up (orthostatic

    hypotension)

Common: (may affect up to 1 in 10 people)

  • dizziness
  • sudden or prolonged periods of low blood pressure (may lead to a heart attack or stroke)
  • flushing
  • blocked nose
  • nausea
  • vomiting
  • diarrhoea
  • general body weakness/feeling weak (asthenia)

Uncommon: (may affect up to 1 in 100 people)

  • tight, painful feeling in the chest (angina)
  • abnormal heart rhythm (arrhythmia)

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 at: 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 Phentolamine solution for injection

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

Store in the original package in order to protect from light.

Store in a refrigerator (2°C – 8°C). Do not freeze.

Do not use this medicine after the expiry date which is stated on the carton after “EXP”. The expiry date refers to the last day of that month.

6. Contents of the pack and other information

What Phentolamine solution for injection contains

  • The active substance is

    phentolamine mesilate. Each ampoule of 1 ml contains 10 mg phentolamine mesilate. This is equivalent to a total of 7.45 mg/ml phentolamine.

  • The other ingredients are: sodium metabisulphite (E223), glucose monohydrate and water for injections.

    What Phentolamine solution for injection looks like and contents of the pack

    Clear, colourless solution, virtually free from visible particles.

    Each pack of Phentolamine solution for injection contains 5 single use ampoules of 1 ml.

    Marketing Authorisation Holder and Manufacturer

    Marketing Authorisation Holder

    ROMA Pharmaceuticals Limited Gibraltar House

    Centrum 100

    Burton-upon-Trent

    DE14 2WE

    Email: medinfo@romapharma.co.uk

    Manufacturer

    Anfarm Hellas S.A.

    61st Km National Road Athens Lamia, Schimatari, Viotias, 320 09, Greece

    This leaflet was last revised in August 2025.

    For information in other formats contact medinfo@ romapharma.co.uk Package leaflet: Information for the user

Phentolamine mesilate 10 mg/ml solution for injection

Phentolamine mesilate Roma No.: Phentolamine - 10mg/ml

ROMA

Printing Inks

P 7467 C P 429 C Black

Cutter

Product NameROMA - Phentolamine - 10mg/ml - LEAFLET
MarketUK
Cutter Name
140mm x 590mm

Fonts Used - Calibri

Roma - Version 1 - February 2025

Originated On Originated By02/07/2025 Operator 003
Amended On Amended By07/07/2025 Operator 60

Asset No. 1231

V3

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 49578/0038

Last revision stated in the text: August 2025 · 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 Phentolamine Mesilate 10 mg/ml solution for injection

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Phentolamine
Strength 10 mg/ml
Pharmaceutical form Solution for injection
Single use, ready-to-use, sterile, clear colourless solution practically free from visible matter.
How is it taken Intravenous, Intramuscular
Excipients Sodium metabisulphite (E223), Glucose monohydrate, Water for injections
Pack sizes 5 ampoule
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 24 months.
Storage Store in the original package in order to protect from light.
Store in a refrigerator (2°C – 8°C). Do not freeze.
Keep this medicine out of the sight and reach of children.
Drug group (ATC) Alpha-adrenergic receptor antagonist
  1. C Cardiovascular system drugs
    1. C04 Peripheral vasodilators
      1. C04A Peripheral vasodilators
        1. C04AB Imidazoline derivatives, peripheral vasodilators
          1. C04AB01 phentolamine
Marketing authorisation PL 49578/0038 (first authorised 6 October 2025)
Marketing authorisation holder Roma Pharmaceuticals Ltd
Codes GTIN 5060739220327 · BNF 02050400

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.