Medication info

Eldokain Cataplasma (Lidocaine)

Prescription medication
Ingredient · strength
Lidocaine›700mg / 1 sheet
Manufacturer / importer
(주)텔콘알에프제약
Appearance
A cataplasm with a unique scent, applied on a non-woven fabric, in a white or translucent white sticky solid form.
Packaging
5 sheets/package
Approval status
Active

MFDS item code 201501623 · Notified 2015.03.26

Summary

Main use
Relief of postherpetic neuralgia
Who uses it
Adults
Adult dosage
Adults: This medication should be applied 1 to 3 sheets once a day on the most painful area of intact skin for a maximum of 12 hours. Application method: Remove from the sealed pouch and apply immediately; it can be cut into smaller sizes with scissors and the release film removed for use. For patients with reduced strength or difficulty in drug loss, it is recommended to apply to a narrow area only. Skin irritation or burning sensation.

Ingredients

Manufacturer
(주)텔콘알에프제약

Efficacy & effects

Relief of postherpetic neuralgia

  • Postherpetic neuralgia
View approved original text

This medication is used to relieve neuralgia that may persist after herpes zoster.

Dosage and Administration

Adult dosage

Adults: This medication should be applied 1 to 3 sheets once a day on the most painful area of intact skin for a maximum of 12 hours. Application method: Remove from the sealed pouch and apply immediately; it can be cut into smaller sizes with scissors and the release film removed for use. For patients with reduced strength or difficulty in drug loss, it is recommended to apply to a narrow area only. Skin irritation or burning sensation.

Precautions

This medication can cause serious side effects if chewed or swallowed by children or pets, so it must be stored and disposed of safely out of reach of children and pets. Using this medication over a large area or for more than 12 hours a day can increase the concentration of the drug in the blood, leading to serious side effects. Patients with allergies to this medication or hypersensitivity to amide local anesthetics should not use it. This medication contains propylene glycol and sodium para-aminosulfate; patients with allergies to these components or a history of asthma should use it with caution. Skin reactions such as blisters, bruising, itching, and rash may appear at the application site, most of which are temporary and mild symptoms. Rarely, severe allergic reactions or symptoms such as difficulty breathing and shock may occur. If such symptoms arise, immediate medical attention should be sought. In cases of overdose, serious symptoms affecting the central nervous and cardiovascular systems, such as dizziness, headache, drowsiness, convulsions, and shortness of breath may occur. Patients with severely impaired liver function should be cautious as drug metabolism may be difficult, increasing the risk of high blood concentrations. It is not recommended to use on damaged or infected skin, and care should be taken to avoid contact with the eyes. If contact occurs, rinse with clean water immediately. Using this medication with other local anesthetics or specific antiarrhythmic drugs may increase the risk of side effects, so consultation with a healthcare professional is advised. During pregnancy, it should be used only when necessary, and caution is advised during breastfeeding as the drug may pass into breast milk. The safety and efficacy of this medication have not been sufficiently established in children, so its use in children is not recommended. If overdose is suspected, blood drug concentration should be measured, and appropriate treatment should be provided based on symptoms, as dialysis will not be effective. After use, hands should be washed thoroughly, and used patches should be folded safely and disposed of in a place that is inaccessible to children and pets.

Side effects and when to seek care immediately

Serious side effects

Hives, angioedema, bronchospasm, difficulty breathing, hypersensitivity, laryngeal spasm, shock, anaphylactoid reaction, asthma attack, difficulty breathing, severe swelling (edema), loss of consciousness, convulsions, spasms, respiratory depression, respiratory arrest, potential liver abnormalities due to severe liver disease, severe allergic reactions, severe swelling or urinary disturbances, severe neurological symptoms.

Mild side effects

  • Blisters
  • bruising
  • burning sensation
  • depigmentation
  • dermatitis
  • discoloration
  • swelling
  • erythema
  • scaling
  • irritation
Show 30 more
  • papules
  • petechiae
  • itching
  • vesicles
  • paresthesia
  • angioedema
  • dermatitis
  • itching
  • neuroasthenia
  • confusion
  • disorientation
  • dizziness
  • headache
  • hypersensitivity
  • decreased sensation
  • lightheadedness
  • metallic taste
  • nausea
  • anxiety
  • pain
  • numbness
  • drowsiness
  • altered taste
  • vomiting
  • visual disturbances (blurriness)
  • flushing
  • tinnitus
  • tremor
  • hypersomnia
  • decrease.

Not everyone experiences these, and they can vary from person to person.

Storage

This medication may be sensitive to air or moisture, so it must be stored in a tightly closed container. It is recommended to maintain a storage temperature between 1°C and 30°C. This will help to preserve the efficacy of the medication for a longer time.

Appearance and packaging

Appearance

A cataplasm with a unique scent, applied on a non-woven fabric, in a white or translucent white sticky solid form.

Package unit

5 sheets/package

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

Questions about this medicine

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For anything that needs medical judgment, consult a doctor or pharmacist.

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.