
Ask a doctor about a prescription for ARGENPAL 42.5 mg CUTANEOUS BAR
Package Leaflet: Information for the User
ARGENPAL 42.5 mg skin stick
Silver nitrate
Read all of this leaflet carefully before you start using this medicine
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Contents of the package leaflet:
Argenpal belongs to a group of medicines called antiseptics and disinfectants. It is used in the following cases:
Do not use Argenpal:
Warnings and precautions
Silver nitrate is a corrosive substance that should only be applied to the damaged area to be treated, avoiding unnecessary stains on the skin.
Treatment with silver nitrate produces a black stain on the skin that disappears over time. Healthcare personnel will not repeatedly apply silver nitrate to the same spot, as the stain may become permanent.
In the treatment of nasal bleeding (anterior epistaxis), healthcare personnel will be careful not to apply the medicine to the same place on both sides of the nasal septum, to avoid possible perforation of the septum.
If any problems occur, administration will be interrupted.
Other medicines and Argenpal
Tell your doctor or pharmacist if you are using or have recently used any other medicines.
It should not be used in conjunction with other medicines in the same area.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medicine.
Your doctor will assess the risk-benefit ratio of using Argenpal, as the efficacy and safety of using silver nitrate in pregnant women are unknown and may affect reproductive capacity.
There is no evidence of effects on the ability to drive vehicles or use machines.
Argenpal should be administered by a healthcare professional, on the skin (cutaneous use).
Each Argenpal skin stick is for single use and application.
With the Argenpal skin stick previously moistened in water for a few seconds, the area to be treated should be brushed for a few seconds, trying to limit its application to the affected area, to avoid the appearance of unnecessary black stains on the skin.
It is recommended to protect the surrounding healthy skin with an oily ointment or cream, such as petroleum jelly.
Finally, the treated area should be covered with a bandage or similar.
The application should be performed exclusively by the doctor and for a brief period, which will depend on the degree of action desired.
Due to its application on the skin, Argenpal sticks are not toxic if used properly, as silver nitrate is normally not absorbed. In case of occurrence, silver nitrate poisoning can be acute or chronic.
Chronic silver nitrate poisoning develops slowly and is due to the continued absorption and penetration of silver compounds into the mucous membranes. It is characterized by the appearance of a bluish-gray skin discoloration (argyria).
Accidental or intentional ingestion of silver nitrate can cause throat and stomach pain, acute gastroenteritis, nausea, vomiting, diarrhea, dizziness, weak and rapid pulse, shallow breathing, and convulsions.
For the treatment of poisoning, your doctor will use sodium chloride, followed by stomach lavage or emetic medications (which induce vomiting) or milk or other demulcents (substances that mimic the protective action of mucous membranes) in abundance. For pain and nervous irritability, pentobarbital sodium (a hypnotic) will be administered at a dose of 0.2 g intravenously, and if necessary, cardiotonics (medications that increase heart rate) will be used, and artificial respiration will be applied to maintain vital signs.
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 medicine and the amount ingested.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following side effects have been observed:
Disorders of the skin and subcutaneous tissue:
Frequent (may affect up to 1 in 10 people):
Argenpal may be irritating, causing skin inflammation (dermatitis), redness, burns, skin discoloration, or bluish-gray skin discoloration (argyria) that disappears over time. After prolonged exposure, skin discoloration or stains may become permanent.
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist, even if it is a possible side effect not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: www.notificaRAM.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep out of the sight and reach of children.
No special storage conditions are required. Store in the original packaging.
Do not use Argenpal after the expiry date stated on the packaging. The expiry date is the last day of the month indicated.
Medicines should not be disposed of via wastewater or household waste. Place the packaging and any unused medicines in the SIGRE
collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and any unused medicines. This will help protect the environment.
The active ingredient is silver nitrate. Each skin stick contains 42.5 mg of silver nitrate.
The other ingredients are: potassium nitrate.
Appearance of the product and packaging contents
Skin stick.
Plastic rod approximately 2.4 mm in diameter and 9.5 cm in length with a product head at the end, white or grayish-white in color.
It is presented in a topaz-colored plastic tube containing 10 skin sticks.
Marketing authorization holder and manufacturer
Marketing authorization holder
Ctra. de Terrassa, 121
08191-Rubí (Barcelona)
Spain
Manufacturer
Ronda de los Olivares, Parcela II, Poligono Industrial Los Olivares
23009-Jaén
This leaflet was approved in February 2015
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.es.
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for ARGENPAL 42.5 mg CUTANEOUS BAR – subject to medical assessment and local rules.