
Ask a doctor about a prescription for BETADINE UNIDOSIS 1.000 mg CUTANEOUS SOLUTION IN SINGLE-DOSE PACKAGING
Leaflet: information for the user
Betadine single-dose 1,000 mg cutaneous solution in single-dose packaging
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, pharmacist, or nurse.
Contents of the leaflet
Povidone-iodine, the active ingredient of this medication, is an antiseptic (which destroys germs that cause infections) that contains iodine.
Betadine is indicated as a general skin antiseptic, for small wounds and superficial cuts, minor burns, or abrasions.
In the hospital setting, it is indicated as an antiseptic for the operating field, puncture sites, small wounds, minor burns, and surgical equipment.
Do not use Betadine single-dose
Warnings and precautions
Consult your doctor, pharmacist, or nurse before starting to use Betadine single-dose.
External use only. Do not ingest. Avoid contact with eyes, ears, and other mucous membranes. Consult your doctor if symptoms persist or worsen.
If used in preparation before an operation, avoid accumulation under the patient. It can cause irritation and rarely severe skin reactions. Chemical burns to the skin can occur due to accumulation. In that case, discontinue use. Do not heat before applying.
Patients with goiter, thyroid nodules, or other non-acute thyroid diseases are at risk of developing hyperthyroidism with the administration of high amounts of iodine. In these patients, it should not be applied for prolonged periods or to extensive skin areas unless strictly indicated. Even at the end of treatment, it is necessary to be alert to early symptoms of possible hyperthyroidism and, if necessary, to monitor thyroid function.
It should not be used before or after a radioactive iodine scan or treatment of thyroid carcinoma with radioactive iodine.
Thyroid function tests should be performed in case of prolonged use.
Newborns and small children are at greater risk of developing hypothyroidism. If used in children, it is essential to monitor the thyroid.
Use is not recommended in children under one year of age.
Inform your doctor or pharmacist if you are using, have recently used, or may need to use any other medication.
Do not use with mercurial derivatives, silver, hydrogen peroxide, or taurolidine (antiseptics).
Continuous use should be avoided in patients undergoing simultaneous therapy with lithium (used in psychiatry).
When used at the same time or after antiseptics with octenidine, transient dark discoloration of the affected areas may appear.
Interaction with diagnostic tests: the use of povidone-iodine can lead to errors in tests with toluidine or guaiacol to determine hemoglobin or glucose in feces or urine. It may also interfere with thyroid tests and treatments with radioactive iodine.
Inform your doctor when you need to undergo any diagnostic test.
Inform your doctor if:
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
Use only if strictly indicated; use should be kept to a minimum. Avoid continuous use.
Its use could cause transient hypothyroidism in fetuses and newborns. Thyroid monitoring may be necessary in children.
You should consult your doctor about use in children between 1 and 2 years of age.
Driving and using machines
Betadine does not affect the ability to drive or use machinery.
Follow the administration instructions for the medication contained in this leaflet or as indicated by your doctor, pharmacist, or nurse. In case of doubt, ask your doctor, pharmacist, or nurse.
For cutaneous use. Wash and dry the affected area before applying the product. Repeat 2 to 3 times a day.
After use, discard any remaining liquid.
If you use more Betadine single-dose than you should
In case of excessive product application and skin irritation, wash the affected area with plenty of water, discontinue treatment, and if irritation continues, consult a doctor.
Symptoms could include abdominal pain, anuria (suppression or decreased urine output), circulatory, respiratory, and metabolic problems. Excess iodine can cause goiter, hypothyroidism, and hyperthyroidism.
In case of accidental ingestion, go to a medical center or call the Toxicology Information Service, phone: 91 562 04 20, indicating the product and the amount used.
If you have any other questions about the use of this medication, ask your doctor, pharmacist, or nurse.
Like all medications, this medication can cause side effects, although not everyone experiences them.
In rare cases where skin irritation or allergy occurs, discontinue treatment and wash the affected area with water.
Rare side effects (affecting 1 to 10 in every 10,000 people) are hypersensitivity and contact dermatitis, which manifests as red skin, small blisters, and itching.
Very rare side effects (affecting less than 1 in every 10,000 people) include anaphylactic reactions (severe allergic reaction), hyperthyroidism with tachycardia and agitation, and angioedema (swelling caused by allergy).
Other side effects of unknown frequency have been hypothyroidism, electrolyte imbalance, metabolic acidosis, acute kidney failure, abnormal blood osmolarity, exfoliative dermatitis, dry skin, skin discoloration, and chemical burns to the skin.
If you consider any of the side effects you are experiencing to be serious or if you notice any side effect not mentioned in this leaflet, inform your doctor or pharmacist.
Reporting side effectsIf you experience any type of side effect, consult your doctor, pharmacist, or nurse, even if it is a possible side effect not listed in this leaflet. You can also report them directly through the Spanish Medication Surveillance System for Human Use (https://www.notificaram.es). By reporting side effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of sight and reach of children.
Do not store at a temperature above 30°C.
Do not use this medication after the expiration date shown on the packaging after CAD or EXP. The expiration date is the last day of the month indicated.
Medications should not be thrown down the drain or into the trash. Deposit the packaging and any unused medications at the SIGRE point in your pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and any unused medications. This will help protect the environment.
Composition of Betadine single-dose per single-dose package of 10 ml
The active ingredient is povidone-iodine 1,000 mg.
The other components (excipients) are: glycerol (E 422), lauryl macrogol ether 9, disodium phosphate, citric acid monohydrate, sodium hydroxide (E 524), potassium iodate, and purified water.
Appearance of the product and package contents
Brown-colored solution.
It is presented in high-density polyethylene packages, with 5 single-dose packages of 10 ml and 50 single-dose packages of 10 ml (clinical packaging).
Only some package sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder
Cooper Consumer Health B.V.
Verrijn Stuartweg 60,
1112 AX Diemen,
Netherlands
Manufacturer
Merignac – Cedex
F-33700
France
You can request more information about this medication by contacting the local representative of the marketing authorization holder:
Vemedia Pharma Hispania, S.A.
C/ Aragón, 182, 5ª planta
08011 Barcelona
Spain
Date of the last revision of this leaflet:June 2020
Detailed and updated information about this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) https://www.aemps.es/
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for BETADINE UNIDOSIS 1.000 mg CUTANEOUS SOLUTION IN SINGLE-DOSE PACKAGING – subject to medical assessment and local rules.