THROMBOPHOB 60,000 Gel, 100 g

Instructions for use for THROMBOPHOB 60,000 Gel, 100 g

Detailed instructions for THROMBOPHOB 60,000 Gel, 100 g

Field of use

• For supporting treatment for acute swelling states after blunt injuries (bruises/bruises) and superficial vein inflammation, provided that this cannot be treated by compression.

Active ingredients / ingredients / ingredients

60000 Ie heparin, sodium salt (from pig)
Ammonia auxiliary substances (+)
Carbomer auxiliary substance (+)
Isopropyl alcohol auxiliary material (+)
Perfume oil auxiliary material (+)
Polyoxyethylene (6) Caprylic acid/caprinsic regalide auxiliary material (+)
Polysorbate 60 HILDVERSTOFT (+)
Water, cleaned auxiliary material (+)

Contradictions

• The medicine must not be used
  • if you are hypersensitive (allergic) against heparin or one of the other components
  • if you have an acute or from the history of known allergic waste of the number of plates of blood (thrombocytopenia type II) by heparin

dosage

• Always apply the preparation 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 medicine is to be applied thinly and evenly to the disease area 2 - 3 times a day.

 

• Duration of the application
  • The medicine must not be used for more than 10 days.

 

• If you have used a larger amount than you should
  • Please contact your doctor or a pharmacist if you have used a larger amount than you should.

 

• If you have forgotten the application
  • Do not apply the double dose if you have forgotten the previous application.

 

• If you cancel the application
  • If you want to interrupt the treatment or end prematurely, please consult your doctor or pharmacist first.

Taking

• apply thin and evenly to the disease area

Patient information

• Special care in the application is required
  • When the occurrence of new symptoms that can indicate thrombosis or pulmonary embolism, such as
    • Swelling and feeling of heat in the affected body part,
    • red and tense skin, possibly blue coloring,
    • Tension and pain in the foot, calf and knee throat (relief in the event of high storage)
    • Suddenly shortness of breath, chest pain and weakness/collapse
  • The presence of a heparin-induced thombocytopenia type II must be excluded and the number of blood (platelet number) must be checked immediately.
  • Regular checks of the platelet values are required for every heparin application.
  • Controls of the platelet number should take place:
    • before starting the heparin gift
    • on the 1st day after the start of the heparin gift
    • then every 3 - 4 days until the end of the heparin treatment
  • If medicinal products are used at the same time, an increased risk of bleeding cannot be excluded. Bruises can occur more frequently or increase in expansion.
  • During the treatment, syringes in the muscle must be avoided because of the risk of bruises (hematoma).
  • The medicine should not be applied to open wounds and/or oozing eczema.
  • The drug is alcoholic and should therefore not come into contact with the eyes or mucous membrane.

Pregnancy

• Previouse Experience with the use of pregnant and breastfeeding has not shown any indications of harmful effects.
• Heparin is not placent agent and does not move into breast milk.

Hints

Miscellaneous

- One of the first treating measures in the surface of the lower limbs is pressure treatment.

- Because of the alcohol content, the gel should not be applied to mucous membranes, open or inflamed skin areas (e.g. sunburn) or come into contact with the eyes because a burning feeling can arise.

Manufacturer:  Nordmark Arzneimittel GmbH & Co., Pinnauallee 4, 25436 Uetersen