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-14% TAPFI 25 mg/25 mg of active ingredient pavement,pcs

TAPFI 25 mg/25 mg of active ingredient pavement,pcs

TAPFI 25 mg/25 mg wirkstoffhaltiges Pflaster

Manufacturers: Pädia GmbH

PZN: 16739747

Dosage: Pflaster

Content: 2 St

Reward Points: 76

Availability: In stock

$10.80

$9.26

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-14% TAPFI 25 mg/25 mg of active ingredient pavement,pcs
  • TAPFI 25 mg/25 mg of active ingredient pavement,pcs
  • TAPFI 25 mg/25 mg of active ingredient pavement,pcs
  • TAPFI 25 mg/25 mg of active ingredient pavement,pcs
  • TAPFI 25 mg/25 mg of active ingredient pavement,pcs
  • TAPFI 25 mg/25 mg of active ingredient pavement,pcs

Instructions for use for TAPFI 25 mg/25 mg of active ingredient pavement,pcs

Application notes

Type of application?
Glue the active ingredient pavement on the affected person (s). The affected skin (s) should be clean, dry and hairless. Press the paving edges vigorously and save the center of the pavement. The pavement should be applied to the skin at least 1 hour before the planned intervention. You must not cut the pavement or cut down elsewhere. Wash your hands thoroughly after use. Avoid accidental contact with eyes, damaged skin and open skin.

Duration of the application?
The duration or duration of the drug depends on the type of intervention. It should therefore be determined in consultation with your doctor.

Overdose?
In the event of an overdose, there may be reduced oxygen transport of red blood cells (methemoglobinemia), disorders of the nervous system such as cramps and consciousness disorders and cardiovascular complaints. If you suspect an overdose, contact a doctor immediately.

In general, pay attention to a conscientious dosage especially in infants, toddlers and older people. If in doubt, ask your doctor or pharmacist about any effects or precautionary measures.

A dosage prescribed by the doctor may differ from the information on the package insert. Since the doctor coordinates you individually, you should therefore apply the medicine according to his instructions.
Dosage
Since the dosage of the drug depends on various factors, your doctor should be tailored to you individually.
Get advice from your doctor or pharmacist.

Application areas

- Superficial anesthesia, especially in connection with:
- Superficial anesthesia in front of needle engravings
- Superficial anesthesia of the skin in smaller operations

Mode of action

How do the ingredients of the drug work?

The medicine consists of a combination of the two active ingredients lidocaine and prilocaine, which belong to the group of local anesthetics. The active ingredients suppress the nerves of the nerves and thus make them insensitive to pain and itching and lead to a local anesthesia.

Composition

based on 10 cm2 plaster = 1 patch
25 mg lidocaine
25 mg prilocaine
20 mg macrogol glycerol hydroxystear
+ Carbomer 974 P
+ Sodium hydroxide for pH value setting
+ Water, cleaned
+ Cellulose
+ Polyethylene film, aluminized
+ Polyethylene acrylate glue

Contradictions

What speaks against an application?

Always:
- Hypersensitivity to the ingredients

Under certain circumstances - speak to your doctor or pharmacist:
- Hereditary enzyme disorder (glucose-6-phosphate dehydrogenase deficiency)
- Reduced oxygen transport of red blood cells (methemoglobinemia)
- Neurodermatitis

What about pregnancy and lactation?
- Pregnancy: Contact your doctor. Various considerations play a role in whether and how the medicine can be used during pregnancy.
- Still -time: According to current knowledge, there is no evidence that the medicine must not be applied during breastfeeding.

If the medicine has been prescribed to you despite a counter -notification, speak to your doctor or pharmacist. The therapeutic benefit can be higher than the risk of using the application.

Side effects

What adverse effects may occur?

- Removal of skin at the application site
- Water storage at the application site
- Bright skin coloring at the application site
- Pain at the application site
- Itching at the application site
- Heat feeling at the application site
- Reduced oxygen transport red bloodkicing (methemoglobinemia)
- Hypersensitivity
- Irritation of the cornea of the eye (cornea)
- Small to large-stained skin damage (skin lesion), especially after a long treatment of children with neurodermatitis or dell warts

If you notice a disorder or change during treatment, contact your doctor or pharmacist.

For information at this point, side effects are taken into account that occurs in at least one of 1,000 patients treated.

Hints

What should you consider?
- Be careful with allergy to local anesthesia (local anesthetics such as articaine, bupivacain, lidocaine, mepivacain, prilocaine, ropivacain)!
- Solving investigators (e.g. poly (oxyethylene) -ratzinus oils) can cause skin irritation.
- There can be medicinal products with which interactions occur. Therefore, you should generally provide the doctor or pharmacist before treatment with a new medicine. This also applies to medicines that you buy yourself, only apply occasionally or that the application has been available for some time.

Detailed instructions for TAPFI 25 mg/25 mg of active ingredient pavement,pcs

Field of use

  • This medicine contains two active ingredients that are called lidocaine and prilocaine. These belong to a group of medicines called local anesthetics.
  • It works by stunning the skin surface for a short time. It is applied to the skin before certain medical interventions. This helps to switch off the pain on the skin. Nevertheless, you may still feel pressure or touch.
  • Adults, young people and children
    • It can be used to anesthesize the skin:
      • a pinstick (e.g. if you get an injection or to take blood),
      • smaller surgical interventions on the skin.

Active ingredients / ingredients / ingredients

25 mg lidocaine
25 mg prilocaine
Acrylic adhesive auxiliary substance (+)
Aluminum foil with plastic coating auxiliary material (+)
Carbomer 974p Hedge substance (+)
Cellulose fleece auxiliary substance (+)
20 mg macrogol glycerol hydroxysteast
Sodium hydroxide auxiliary substance (+)
Polyethylene auxiliary substances (+)
Water, cleaned auxiliary material (+)

Contradictions

  • This medicine must not be used,
    • if you are allergic to lidocaine or prilocaine, other similar local anesthetics or one of the other components of this medicine.

dosage

  • Always apply this medicine as described or exactly according to your doctor, pharmacist or medical staff. Ask your doctor, pharmacist or medical staff if you are not sure.
  • Where the active ingredient plaster is glued on, how many plasters are used and how long it linger on the skin depends on what it is needed for.
  • Your doctor, pharmacist or medical staff will stick the active ingredient pavement or show you how to use it correctly.
  • Do not apply the patch on the following skin areas:
    • Cuts, abrasions or wounds
    • Places with rash or eczema
    • Near the eyes
    • In the mouth
  • Application on the skin in front of smaller interventions (as with a needle stitch or smaller skin surgery):
    • The active ingredient patch is glued on the skin. Your doctor, pharmacist or medical specialist staff will tell you where to stick it.
    • The active ingredient pavement is removed immediately before the procedure.
    • In adults and adolescents from the age of 12, one or more plasters are usually applied.
    • In adults and adolescents from the age of 12, the active ingredient pavement is glued on at least 60 minutes before the procedure. However, do not stick it more than 5 hours before the procedure.
    • In children, it depends on age how many active ingredient plasters are used and how long these are used. Your doctor, pharmacist or medical staff will tell you how many active ingredient plasters you need and when they should be glued on.
  • Children
    • Application on the skin in front of smaller interventions (as with a needle stitch or smaller skin surgery):
      • Expensive time: approx. 1 hour.
    • Newborns and infants aged 0-2 months: A pavement -containing patch is glued to the skin surface to be treated.
      • Expensive time: at most 1 hour. Only one single dose may be applied within 24 hours.
      • Due to its size, the active ingredient patch is not suitable for use on certain parts of the body of newborns and infants.
    • Infants between the ages of 3 and 11 months: Up to two active ingredient plasters are glued to the skin surface to be treated.
      • Expensive time: approx. 1 hour, at most 4 hours.
    • Children from 1 - 5 years: Up to 10 active ingredient plasters are glued to the skin surface to be treated.
      • Expensive time: approx. 1 hour, a maximum of 5 hours.
    • Children from 6-11 years: Up to 20 pavement containing active ingredients are glued to the skin surface to be treated.
      • Expensive time: approx. 1 hour, a maximum of 5 hours.
    • Within a period of 24 hours, a maximum of 2 doses may be used in children over 3 months as listed above.
    • This preparation can be used in children with neurodermatitis (a skin disease, which is also called "atopic dermatitis"), but the exposure time is then no more than 30 minutes.
  • If you apply the active ingredient pavement, it is important that you follow the following instructions exactly:
    • The pavement should be glued on at least 1 hour before the planned intervention (except for patients with neurodermatitis).
    • If necessary, remove body hair in the corresponding skin area before using. The active ingredient pavement must not be cut or otherwise disintegrated.
  • Application on the skin before removing dellwarten
    • The pavement can be used in children and adolescents with neurodermatitis (a skin disease that is also called "atopic dermatitis").
    • The usual dose depends on the age of the child and is used for 30 to 60 minutes (30 minutes in children/adolescents with neurodermatitis). Your doctor, pharmacist or medical specialist staff will tell you how many plasters you should apply.

 

  • If you have used more plasters than you should
    • If you have used more plasters than your doctor, pharmacist or the medical staff told you, inform them immediately, even if you do not notice any signs of illness.
    • Complaints after use of too many plasters are listed below. It is unlikely that the symptoms will occur if the preparation is used as recommended.
      • Feeling of drowsiness or dizziness
      • Tingling the skin around the mouth and deafness of the tongue
      • Unusual taste
      • See blurry
      • Noise
      • There is also the risk of "acute methemoglobinemia" (a problem with the blood pigment concentration). This is more likely if certain medicines have been taken at the same time. If this occurs, the skin becomes bluish due to the oxygen deficiency.
    • In severe cases of overdose, signs of illness such as seizures, low blood pressure, slow breathing, exposing breathing and changing heartbeat can occur.
    • These effects can be life -threatening.

 

  • If you have any further questions about the application of this medicine, please contact your doctor or pharmacist or the medical staff.

Taking

  • If you apply the active ingredient pavement, it is important that you follow the following instructions exactly:
    • It should be glued on at least 1 hour before the planned intervention (except for patients with neurodermatitis).
    • If necessary, entertainbefore using body hair in the corresponding skin area. The active ingredient pavement must not be cut or otherwise disintegrated.
    • 1. Make sure that the skin surface to be numb is clean and dry.
    • Bend the protruding aluminum wing back on the corner of the pavement. Now grab the skin -colored pavement side with the other hand. Make sure that both layers on the corner are well separated before continuing.
    • 2. Now, as shown in the figure, pull apart adhesive surface and protective film.
    • Make sure that you do not touch the white round pillow that contains the active ingredients (lidocaine/prilocaine).
    • 3. Do not press the middle of the active ingredient pavement. This could lead to the emulsion leaving and the adhesive surface is not adequately liable. Press the pavement firmly on the edges so that it sticks well on the skin.
    • 4. On the edge of the active ingredient pavement, the time can be noted to which it was glued on. (For example, a ballpoint pen is suitable.)
    • 5. Let the active ingredient patch work for at least 1 hour (exception: patients with neurodermatitis).
    • In children under 3 months, the active ingredient plaster must not be applied for more than an hour.
    • 6. Remove the active ingredient pavement after the corresponding exposure time.

Patient information

  • Warnings and Precautions
    • Please speak to your doctor, pharmacist or the medical staff before using the medicine,
      • if you or your child have a rare congenital disease, called "glucose-6 phosphate dehydrogenic lack", which affects the blood;
      • if you or your child have a problem with the concentration of the blood pigment methemoglobin in the blood, called "methemoglobinemia;
      • do not apply the patch on surfaces with rash, cuts, skin abrasions or other open wounds. If there is one of these problems, speak to your doctor, pharmacist or medical staff before using the pavement;
      • if you or your child have neurodermatitis (itchy skin disease, also called "atopic dermatitis"), a shorter exposure time can be sufficient. An exposure period of more than 30 minutes can lead to an increased occurrence of local skin reactions.
    • Avoid that the active ingredient emulsion gets into the eyes because this can cause irritation. If the emulsion accidentally reaches your eye, you should immediately rinse it well with lukewarm water or saline (sodium chloride solution).
    • Make sure that nothing comes into your eye until the feeling has returned.
    • If you apply the preparation before vaccinations with living vaccines (e.g. tuberculosis-
      Vaccinations), you should see your doctor or medical staff again in the given period to check the Imperson Result.
    • Children and adolescents
      • In infants/newborns under 3 months, up to 12 hours after the pavement has been applied, a temporary, clinically non -significant increase in the concentration of the blood pigment methemoglobin in the blood ("Methemoglobinemia") is observed.
      • The effectiveness of the pavement in blood sampling on the heel of newborns could not be confirmed in clinical studies.
      • It should not be used in children under 12 months that are treated at the same time as other drugs that affect the concentration of the blood pigment methemoglobin in the blood ("methemoglobinemia") (e.g. sulfonamides).
      • The preparation should not be used in premature babies.

 

  • Wateriness and ability to operate machines
    • This preparation has no or a negligible influence on the traffic and the ability to use machines if it is used in the recommended doses.

Pregnancy

  • If you are pregnant or breastfeed, or if you suspect to be pregnant or intend to get pregnant, ask your doctor or pharmacist for advice before using this drug.
  • Pregnancy
    • It is unlikely that the occasional application during pregnancy will have a negative impact on the fetus.
  • Breastfeeding
    • The active ingredients (lidocaine and prilocaine) pass into breast milk. However, the amount is so low that there is generally no risk for the child.
  • Reproductive ability
    • Animal studies showed no impairment of male or female reproductive ability.

Hints

Read the package supplement and ask your doctor or pharmacist for risks and side effects.

Manufacturer:  Pädia GmbH, von-Humboldt-Straße 1, 64646 Heppenheim

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