IBUTOP Pain gel, 150 g

Instructions for use for IBUTOP Pain gel, 150 g

Detailed instructions for IBUTOP Pain gel, 150 g

Field of use

• The preparation is a pain -relieving and anti -inflammatory drug for rubbing into the skin.
• Application areas
  • For sole or supportive external treatment
    • Swelling or inflammation of the soft tissues close to the joints (e.g. bursa, tendons, tendon sheaths, ligaments and joint capsule), - sports and accident injuries such as bruises, sprains, struggle.

Mode of action

The special thing about ibutop pain gel (pack size: 150 g):

The active ingredient ibuprofen contained in ibutop pain gel (pack size: 150 g) has an anti -inflammatory effect and relieves the pain.

Active ingredients / ingredients / ingredients

Ibutop pain gel (pack size: 150 g) contains:

1 g ibutop pain gel contains 50 mg ibuprofen.

The other components are: 2-propanol, poloxamer 407, dimethylisosorbide, medium-chain triglycerides, bitter orange flower oil, lavender oil, cleaned water

Contradictions

• The medicine must not be used
  • if you are hypersensitive (allergic) against the active ingredient ibuprofen, other components of the drug or against other pain and rheumatism (non-steroidal anti-inflammatory drugs);
  • on open injuries, inflammation or infections of the skin, as well as on eczema or on mucous membranes;
  • under airtight associations;
  • in the last third of the pregnancy.

dosage

• Always apply the medicine exactly according to the instruction. Please ask your doctor or pharmacist if you are not quite sure.
• Unless otherwise prescribed by the doctor, the usual dose is:
  • The gel is used 3 times a day. Depending on the size of the painful area to be treated, a 4 - 10 cm long gel strand is required accordingly 2 - 5 g gel (100 - 250 mg ibuprofen).
  • The maximum total daily dose is 15 g gel according to 750 mg ibuprofen.

 

• Duration of the application
  • The practicing doctor will decide about the length of the treatments. As a rule, an application over 2 - 3 weeks is sufficient. The therapeutic benefit of an application beyond this period is not proven.
  • Please speak to your doctor or pharmacist if you have the impression that the effect of the drug is too strong or too weak.

 

• If you have used a larger amount than you should
  • If the recommended dosage is exceeded during use on the skin, the gel should be removed and washed off with water. When using much too large quantities or accidental intake of the drug, the doctor must be notified.
  • There is no specific antidote (antidote).

Taking

• Only for external use! Do not take!
• The gel is applied to the skin and lerubbed into the skin.
• An increased penetration of the active ingredient through the skin can be achieved by using the ondophoresis (a special form of electrotherapy). The gel must be applied under the cathode (minus pole). The current strength should be 0.1 - 0.5 mA per 5 cm2 electrode interface, the application time approx. 10 minutes.

Patient information

• Particular caution when using the drug is required
  • The preparation should not be used in children and adolescents under the age of 14, since there is no sufficient examinations for this age group.
  • Patients suffering from asthma, hay fever, nasal mucosal swelling (so-called nasal polyps) or chronically obstructive respiratory diseases or chronic respiratory infections (particularly coupled with hay fever-like phenomena), and patients with hypersensitivity to pain and rheumatism are used when using the medicine (so-called Analgetics intolerance/analgesic asthma), local skin and mucosal swelling (so-called quincke-edema) or urticaria rather endangered than other patients.
  • In these patients, the medicine may only be used under certain precautionary measures and direct medical control. The same applies to patients who also react hypersensitive to other substances, such as: B. with skin reactions, itching or nettle fever.
  • It should be ensured that children with their hands do not get in touch with the skin areas grated with the medicine.
  • In the event of complaints that last for more than 3 days, a doctor should be consulted.

 

• Wateriness and operating machines
  • There are no special precautions required.

Pregnancy

• Ask your doctor or pharmacist for advice before using the drug.
• Pregnancy
  • If pregnancy is determined during the application of the drug, the doctor must be notified. You can only use ibuprofen in the first and second thirds of pregnancy after consultation with your doctor. In the last third of pregnancy, the preparation must not be used due to the increased risk of complications for mother and child.
• Breastfeeding
  • The active ingredient ibuprofen and its dismantling products pass into breast milk in only small quantities. Since adverse consequences for the infant have not yet become known, an interruption of breastfeeding will generally not be necessary if used briefly.
  • However, a daily dose of 15 g gel should not be exceeded and an early weaning should be considered if used for a long time. In order to avoid recording by the infant, breastfeeding may not apply the medicine in the chest area.

Hints

• Particular caution when using the drug is required
  • The preparation should not be used in children and adolescents under the age of 14, since there is no sufficient examinations for this age group.
  • Patients suffering from asthma, hay fever, nasal mucosal swelling (so-called nasal polyps) or chronically obstructive respiratory diseases or chronic respiratory infections (particularly coupled with hay fever-like phenomena), and patients with hypersensitivity to pain and rheumatism are used when using the medicine (so-called Analgetics intolerance/analgesic asthma), local skin and mucosal swelling (so-called quincke-edema) or urticaria rather endangered than other patients.
  • In these patients, the medicine may only be used under certain precautionary measures and direct medical control. The same applies to patients who also react hypersensitive to other substances, such as: B. with skin reactions, itching or nettle fever.
  • It should be ensured that children with their hands do not get in touch with the skin areas grated with the medicine.
  • In the event of complaints that last for more than 3 days, if a doctor is consulted.

• Wateriness and operating machines
  • There are no special precautions required.

Manufacturer:  axicorp Pharma GmbH, Max-Planck-Straße 36b, 61381 Friedrichsdorf