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QUIROCROM 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION

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About the medicine

How to use QUIROCROM 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION

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This page provides general information and does not replace a doctor’s consultation. Always consult a doctor before taking any medication. Seek urgent medical care if symptoms are severe.

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Introduction

Leaflet: information for the user

Quirocrom 20 mg/ml + 0.70 ml/ml cutaneous solution

chlorhexidine digluconate / isopropyl alcohol

Read the entire leaflet carefully before starting to use this medication, as it contains important information for you.

Follow the administration instructions for the medication contained in this leaflet or as indicated by your doctor or nurse.

  • Keep this leaflet, as you may need to read it again.
  • If you need advice or more information, consult your pharmacist.
  • If you experience side effects, consult your doctor or nurse, even if they are side effects that do not appear in this leaflet. See section 4.
  • You should consult a doctor if it worsens or does not improve.

Contents of the leaflet

  1. What is Quirocrom and what is it used for
  2. What you need to know before starting to use Quirocrom
  3. How to use Quirocrom
  4. Possible side effects
  5. Storage of Quirocrom
  6. Package contents and additional information

1. What is Quirocrom and what is it used for

Quirocrom is a cutaneous solution of chlorhexidine digluconate 20 mg/ml and isopropyl alcohol 0.70 ml/ml, used as a skin antiseptic before performing invasive medical procedures, such as injections, insertion of intravascular catheters, minor and major surgery in adults and children.

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2. What you need to know before starting to use Quirocrom

Do not useQuirocromif:

If you are allergic (hypersensitive) to chlorhexidine digluconate, isopropyl alcohol, or any of the other components of this medication (included in section 6).

Warnings and precautions:

Quirocrom is for external use on the skin only. Do not ingest or inhale.

  • The solution is flammable. Cases of fire in the operating room have been reported, resulting in severe burns to the patient.

The risk of fire in the operating room is high when using an ignition source (electrosurgical units, lasers, fiber optic light sources, high-speed drills/burs...) in combination with a combustion source (such as cloths, towels...) and an oxidizing agent (oxygen, air, nitrous oxide...).

To reduce the risk of fire:

Do not use electrocauterization procedures or other ignition sources until the skin is completely dry.

Remove any soaked material, gauzes, or gowns before starting the intervention.

Do not use excessive amounts and avoid accumulating the solution in skin folds, under the patient, or soaking sheets or other materials in direct contact with the patient.

When applying an occlusive dressing to areas previously exposed to Quirocrom, be careful not to leave excess product before applying the dressing.

Reduce the oxygen supply or any other oxidizing agent to the minimum necessary. Procedures performed on the head, neck, and upper chest (above T5) and the use of an ignition source near an oxidizing agent put the patient at risk of suffering a surgical fire.

Quirocrom may, in rare cases, cause severe allergic reactions that can lead to a decrease in blood pressure and even loss of consciousness. The first symptoms of a severe allergic reaction may be skin rash or asthma. If you notice these symptoms, stop using Quirocrom and contact your doctor as soon as possible (see section 4: Possible side effects).

Avoid prolonged contact with the skin.

Quirocrom should not be used:

  • Near the eyes or sensitive areas (mucous membranes), as it may cause irritation, pain, redness, vision problems, chemical burns, and eye damage. In case of contact with the eyes or mucous membranes, the affected area should be rinsed immediately with plenty of water.

Avoid contact with the brain, meninges (membranes surrounding the brain and spinal cord), and middle ear

Quirocrom should not come into contact with the eyes due to the risk of visual damage. If it comes into contact with the eyes, rinse immediately and abundantly with water. In case of irritation, redness, or pain in the eyes, or visual disturbances, consult a doctor immediately.

Severe cases of persistent corneal injury (injury to the surface of the eye) that may require a corneal transplant have been reported when similar products have accidentally come into contact with the eyes during surgical interventions, in patients under general anesthesia (deep, painless sleep).

  • On open wounds
  • On the inner ear (middle ear)
  • In direct contact with neural tissue (e.g., brain and spinal cord)

Quirocrom should only be applied gently to the skin. If the solution is applied too vigorously to fragile or sensitive skin, or after repeated use, it may cause erythema, inflammation, itching, dry skin, and/or peeling, and pain. If you notice any of these reactions, stop administering Quirocrom.

Children

Use with caution in neonates, especially in preterm infants. Quirocrom may cause chemical burns to the skin.

Other medications and Quirocrom

Tell your doctor or nurse if you are using, have recently used, or may need to use any other medication.

Inform your doctor or nurse if you have recently been administered a vaccine or an injection for a skin test (epicutaneous tests for detecting allergies).

The use of different antiseptics should be avoided to minimize the risk of possible interference between them.

Do not use Quirocrom with anionic soaps, iodine, heavy metal salts, and acids.

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or nurse before using this medication.

It is unknown whether chlorhexidine digluconate or isopropyl alcohol is excreted in breast milk. Since many medications are excreted in breast milk, caution should be exercised when administering Quirocrom to breastfeeding women.

Driving and using machines

Quirocrom does not alter the ability to drive or operate machines.

3. How to use Quirocrom

Your doctor or nurse will select the volume of solution based on the area to be treated and the area to be covered. Apply the product gently to the skin area that needs to be prepared. Do not dilute.

In case of doubt, ask your doctor or nurse.

If you use more Quirocrom than you should

In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.

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4. Possible side effects

Like all medications, this medication can cause side effects, although not everyone experiences them.

Very rare side effects (less than 1 in 10,000 people) observed in the skin and subcutaneous tissue are:

Skin irritation, including: erythema, rash, urticaria, pruritus, and blisters or vesicles at the administration site. Other local symptoms may be: burning sensation on the skin, pain, and inflammation.

Other possible side effects, for which the frequency is unknown, are:

-Allergic reactions, including anaphylactic shock.

-Eye irritation, pain, hyperemia, vision problems, chemical burns, and eye damage in cases of accidental contact.

-Chemical burns in neonates.

-Allergic skin disorders such as dermatitis (skin inflammation), pruritus (itching), erythema (skin redness), eczema, rash, urticaria (hives), skin irritation, and blisters.

-Corneal injury (injury to the surface of the eye) and permanent eye damage, including permanent vision loss (after accidental eye exposure during surgical interventions in the head, face, and neck) in patients under general anesthesia (deep, painless sleep).

Stop using Quirocrom and seek medical attention immediately if you experience any of the following reactions: swelling of the face, lips, tongue, or throat; red, itchy skin rash; wheezing or difficulty breathing; feeling of fainting and dizziness; strange metallic taste in the mouth; collapse. You may be having an allergic reaction.

Reporting side effects

If you experience any side effects, consult your doctor or pharmacist, even if they are possible side effects that do not appear in this leaflet. You can also report them directly through the Spanish Medicines and Healthcare Products Agency (AEMPS) http://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medication.

5. Storage of Quirocrom

This medication is flammable. Avoid exposing the container and its contents to open flames during use, storage, and disposal of the product.

Do not store above 30 °C.

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

Do not use this medication after the expiration date stated on the container after "CAD". The expiration date is the last day of the month indicated. The medication should be discarded 6 months after opening.

Medications should not be thrown away in drains or trash. Ask your pharmacist how to dispose of the containers and medications you no longer need. This will help protect the environment.

6. Package contents and additional information

Composition of Quirocrom

The active ingredients are chlorhexidine digluconate 20 mg/ml and isopropyl alcohol 0.70 ml/ml.

The other components are purified water, Allura AC Red (E-129), and curcumin (E-100).

Appearance of the product and package contents

Transparent, reddish-colored solution presented in 100 ml and 250 ml plastic bottles. It is presented in:

  • Clinical package of 30 bottles of 100 ml
  • Clinical package of 15 bottles of 250 ml

Marketing authorization holder and manufacturer

Laboratorios Salvat, S.A.

C/ Gall, 30-36 - 08950

Esplugues de Llobregat

Barcelona - Spain

Date of the last revision of this leaflet: July 2024

Updated and detailed information on this medication is available on the website of the Spanish Agency for Medicines and Healthcare Products (AEMPS) http://www.aemps.gob.es

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Dermatology 21 years exp.

Dr Tomasz Grzelewski is an MD, PhD specialist in allergy, paediatrics, general practice and sports medicine, with a clinical focus on dermatology, endocrinology, allergology and sports-related health. He has more than 20 years of clinical experience and completed his medical training at the Medical University of Łódź, where he defended his PhD thesis with distinction. His doctoral research was recognised by the Polish Society of Allergology for its innovative contribution to the field. Throughout his career, he has gained extensive expertise in diagnosing and managing a wide range of allergic and paediatric conditions, including modern allergen desensitisation techniques.

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Frequently Asked Questions

Is a prescription required for QUIROCROM 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION?
QUIROCROM 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION does not require a prescription in Spain. You can check with a doctor online whether this medicine may be appropriate for your situation.
What is the active substance in QUIROCROM 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION?
The active ingredient in QUIROCROM 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION is chlorhexidine, combinations. This information helps identify medicines with the same composition but different brand names.
Who manufactures QUIROCROM 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION?
QUIROCROM 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION is manufactured by Laboratorios Salvat S.A.. Pharmacy brands and packaging may differ depending on the distributor.
Which doctors can assess the use of QUIROCROM 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION online?
Doctors such as Family doctors, Psychiatrists, Dermatologists, Cardiologists, Endocrinologists, Gastroenterologists, Pulmonologists, Nephrologists, Rheumatologists, Hematologists, Infectious disease physicians, Allergists, Geriatricians, Paediatricians, Oncologists may assess whether QUIROCROM 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION is appropriate, depending on your situation and local regulations. You can book an online consultation to discuss your symptoms and possible next steps.
What are the alternatives to QUIROCROM 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION?
Other medicines with the same active substance (chlorhexidine, combinations) include BACTISEPTIC PHARMA 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION, BACTISEPTIC PHARMA ORANGE 20 mg/mL + 0.70 mL/mL CUTANEOUS SOLUTION, CHLORAPREP ORANGE 20mg/ml + 0.70 ml/ml CUTANEOUS SOLUTION. These may have different brand names or formulations but contain the same therapeutic ingredient. Always consult a doctor before switching or starting a new medicine.
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