Milgamma protekt, 90 tablets

  • Price VND VND 1.400.000

  • Price Kyat Ks 150.000

  • Prices not incl. VAT, plus shipping costs.

Art. no: 1529731

Made in: Germany

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For nerve damage (neuropathies) caused by vitamin B1 deficiency, milgamma protect with benfotiamine For the treatment of vitamin B1 deficiency. In this way, foot complaints such as tingling, burning or numbness can be alleviated at their source.
Product information

For nerve damage (neuropathies) caused by vitamin B1 deficiency.

milgamma protect with benfotiamine

For the treatment of vitamin B1 deficiency. In this way, foot complaints such as tingling, burning or numbness can be alleviated at their source.

Your choice for nerve damage caused by vitamin B1 deficiency
Tingling, burning or aching feet prevent many people from sleeping at night. Nerve damage, so-called neuropathies, can be a possible cause. Those affected often do not know that a vitamin B1 deficiency can also trigger or exacerbate these neuropathies. If you compensate for this deficit, you can alleviate your foot problems. People with diabetes in particular can have an increased risk of vitamin B1 deficiency and neuropathies. The increased blood sugar can damage the nerves and at the same time promote a vitamin B1 deficit.

Benfotiamine is the "better" vitamin B1

  • for the treatment of vitamin B1 deficiency as a possible cause of diseases of the nerves
  • Fat-soluble vitamin B1 precursor with 5 times higher bioavailability than normal vitamin B1¹
  • well tolerated
  • also suitable for long-term use

milgamma protekt can compensate for the vitamin B1 deficiency and alleviate the symptoms. The special thing is the active ingredient benfotiamine. The fat-soluble precursor of vitamin B1 is absorbed 5 times better by the body than "simple" vitamin B1 (thiamine). What many do not know: A vitamin B1 deficiency can also cause or worsen nerve damage. It is particularly common in diabetes, and vitamin B1 is increasingly excreted through the kidneys. Diabetics with neuropathies should therefore definitely compensate for the vitamin B1 deficit.

Diabetes has an increased risk of vitamin B1 deficiency

  • Significantly lower vitamin B1 concentration in the blood of diabetics² than in healthy people
  • increased excretion of vitamin B1 through the kidneys²
  • Type 2 diabetics often get less vitamin B1 from food than healthy people.³
  • The increased need for vitamin B1 often cannot be met through normal nutrition.


THE MOST FREQUENT CAUSES OF NERVE DISORDERS DUE TO VITAMIN B1 DEFICIENCY AT A GLANCE

DIABETES MELLITUS AND SPECIAL METABOLIC DISEASES
Around 30% of diabetics in Germany have developed neuropathy. Those affected often do not know that a vitamin B1 deficiency can also contribute to neuropathies and even worsen them. It is all the more important to provide the body with sufficient vitamin B1.

MALNUTRITION AND MALNUTRITION
People who eat a very unbalanced diet and mainly consume white flour products run the risk of not taking in enough vitamin B1. A lot of coffee and black tea or raw fish also inhibit the absorption of the vitamin from food. Excessive alcohol consumption can also promote vitamin B1 deficiency.

CHRONIC GASTROINTESTINAL DISEASES
Anyone who cannot eat enough or suffers from diseases of the gastrointestinal tract such as long-term inflammation or gluten intolerance can develop a vitamin B1 deficiency. In contrast, a vitamin B12 deficiency can often be caused by impaired utilization and absorption of vitamin B12 in the intestine, for example due to the intake of acid blockers, or in connection with a vegetarian or vegan diet.

Application :

  • Take 1 film-coated tablet daily whole with some liquid
  • To treat neuropathies resulting from a vitamin B1 deficiency, milgamma protekt should be taken for at least 3 weeks.
  • suitable for long-term use
  • Keep out of reach of children!

In the case of sensory disturbances caused by diabetic neuropathy, the combination of alpha-lipoic acid and benfotiamine can be useful. Here we recommend the supplementary intake of Thiogamma.

- Prevention and treatment of vitamin B1 deficiency
- Treatment of nervous disorders due to vitamin B1 deficiency
- Treatment of cardiovascular disease due to vitamin B1 deficiency
The drug is given primarily in the case of proven deficiency states, if the vitamin B1 deficiency is not eliminated through nutrition can be.
A vitamin B1 deficiency can occur, for example, in malnourishment and malnutrition, parenteral nutrition, zero diet, dialysis, resoption disorder, chron. Alcoholism, increased need and diabetes mellitus occur.

active ingredients

  • 300 mg benfotiamine

ingredients

  • Croscarmellose sodium
  • hypromellose
  • Partial glycerides, long-chain
  • Silica, colloidal
  • Sodium saccharine
  • cellulose, microcrystalline
  • Povidone K30
  • macrogol
  • titanium dioxide
  • talc

More product information

Indication :

  • The drug is a vitamin supplement.

  • field of use

    • Secured areas of application for the mono-preparations are exclusively therapy or prophylaxis of clinical vitamin B1 deficiencies, if these cannot be remedied through nutrition.

    • The clinically proven vitamin B1 deficiency can occur with:

      • Malnutrition and malnutrition (e.g. beriberi), parenteral nutrition over a long period of time, zero diet, hemodialysis, malabsorption, chronic alcoholism (alcoholic cardiomyopathy, Wernicke encephalopathy, Korsakoff syndrome), increased needs (e.g. pregnancy and lactation).

    • Treatment of neuropathies and cardiovascular disorders caused by vitamin B1 deficiency.

Dosage :

  • Always take the medicine exactly as described in the package leaflet or as your doctor or pharmacist has told you.

  • Please check with your doctor or pharmacist if you are not sure.

  • The following information applies unless your doctor has prescribed the preparation differently. Please follow the instructions for use, otherwise the tablets cannot work properly!

    • The recommended dose is 1 film-coated tablet once a day.

    • For the therapy of neuropathies, the preparation should initially be taken over a period of at least 3 weeks. The further treatment is then carried out according to the therapeutic success.

  • duration of use

    • The duration of the intake depends on the therapeutic success.

    • If after four weeks no or too little effect is recognizable, the therapy of the symptoms should be reviewed.

    • Please talk to your doctor or pharmacist if you have the impression that the effect is too strong or too weak.

  • If you take more than you should:

    • In general, no medical measures are required.

  • If you forget to take a dose

    • Do not take a double dose to make up for a forgotten dose. Try to take the medicine regularly in the future.

  • If you stop taking it

    • If you stop taking the medicine, you risk the success of the treatment.

    • If you notice any unpleasant side effects, talk to your doctor about further treatment.

  • If you have any further questions on taking the medicine, ask your doctor or pharmacist.

way :

  • The film-coated tablets are swallowed whole with some liquid.

Side effects :

  • Like all medicines, this can also have side effects, although not everyone gets them.

  • The evaluation of side effects is based on the following frequency information:

    • Very common: affects more than 1 in 10 people

    • Common: affects 1 to 10 users in 100

    • Uncommon: affects 1 to 10 users in 1,000

    • Rare: affects 1 to 10 users in 10,000

    • Very rare: affects less than 1 in 10,000 people

    • Not known: frequency cannot be estimated from the available data

  • Significant side effects or signs to look out for and actions to take if affected:

    • If you are affected by any of the side effects listed below, stop taking the preparation and consult your doctor as soon as possible.

    • In isolated cases, hypersensitivity reactions can occur (urticaria, skin rash).

    • In clinical studies isolated cases of gastrointestinal disorders such. B. Nausea or other complaints are documented. A causal relationship with vitamin B1 and a possible dose dependency have not yet been sufficiently clarified.

  • If you get any side effects, talk to your doctor, pharmacist or nurse. This also applies to side effects that are not listed in this leaflet.

Interactions :

  • Taking with other medicines:

    • Tell your doctor or pharmacist if you are using, have recently used or might use any other medicines.

    • Thiamine is inactivated by 5-fluorouracil (a drug used to treat cancer) because 5-fluorouracil competitively inhibits the phosphorylation of thiamine to thiamine pyrophosphate.

Contraindications :

  • The medicine should not be taken if you

    • are allergic to benfotiamine, thiamine (chemical name for vitamin B1), or any of the other ingredients of this medicine.

Pregnancy and lactation :

  • If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.

  • pregnancy

    • If you are pregnant, this drug is only useful for treating a proven vitamin B1 deficiency due to the amount of active ingredient. Therefore, you may only use the preparation if your treating doctor considers this to be absolutely necessary. During pregnancy, the recommended daily intake for vitamin B1 is 1.2 mg in the 2nd trimester and 1.3 mg in the 3rd trimester. The safety of using higher than the daily recommended dose has not yet been proven.

  • lactation

    • If you are breastfeeding, this drug is only useful for treating a proven vitamin B1 deficiency due to the amount of active ingredient. Therefore, you may only use the preparation if your treating doctor considers this to be absolutely necessary. When breastfeeding, the recommended daily intake for vitamin B1 is 1.3 mg. The safety of using higher than the daily recommended dose has not yet been proven. Vitamin B1 passes into breast milk.

Patient Notes :

  • Driving and using machines:

    • There are no special precautions required.

The total dose should not be exceeded without consulting a doctor or pharmacist.

Type of application?
Take the medicine with liquid (e.g. 1 glass of water).

Duration of use?
The duration of use depends on the type of symptoms and/or the course of the disease and the success of the treatment. It should therefore be determined in consultation with your doctor.
To treat nerve diseases caused by a lack of vitamin B1, the drug should be used for at least 3 weeks at the beginning. Further treatment depends on the success of the treatment.

overdose?
No overdose symptoms are known to date. If in doubt, consult your doctor.

In general, pay attention to a conscientious dosage, especially for infants, small children and the elderly. If in doubt, ask your doctor or pharmacist about any effects or precautions.

A dosage prescribed by the doctor may deviate from the information on the package leaflet. Therefore, since the doctor adjusts them individually, you should use the medicine according to his instructions.

dosage

General dosage recommendation:
group of people single dose total dose time
All ages 1 tablet 1 time per day regardless of the meal

What speaks against an application?

- Hypersensitivity to the ingredients

What about pregnancy and lactation?
- Pregnancy: consult your doctor. Various considerations play a role in whether and how the drug can be used during pregnancy.
- Breast-feeding: consult your doctor or pharmacist. He will examine your particular starting position and advise you accordingly as to whether and how you can continue breastfeeding.

If you have been prescribed the drug despite a contraindication, talk to your doctor or pharmacist. The therapeutic benefit can be higher than the risk that the use entails in the event of a contraindication.

What adverse effects may occur?

- Hypersensitivity
- Hives (urticaria)
- Skin rash
- Gastrointestinal tract disease
- Nausea
- Gastrointestinal complaints

If you notice any discomfort or changes during treatment, contact your doctor or pharmacist.

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

What should you consider?
- Be careful if you are allergic to binding agents (e.g. carboxymethyl cellulose with the E number E 466)!
- Be careful if you are allergic to the sweetener saccharin (E number E 954)!
- There may be medicines with which interactions occur. You should therefore generally tell your doctor or pharmacist about any other medicine you are already using before starting treatment with a new medicine. This also applies to medicines that you buy yourself, use only occasionally or have been using for some time.

How does the ingredient of the medicine work?

The active ingredient benfotiamine is a fat-soluble precursor (prodrug) of thiamine (vitamin B1) and is very well absorbed in the body and quickly converted into its effective form. Like thiamine (vitamin B1), the active ingredient is essential for the functioning of the nervous system and plays an important role in carbohydrate metabolism.

What is included in medicines?
 

The amounts given are based on 1 tablet.
 
Active substance benfotiamine 300mg                
Excipient cellulose, microcrystalline +
Additive talc +
Excipient Povidone K30 +
Excipient Silicon dioxide, colloidal +
Excipient croscarmellose sodium +
Excipient partial glycerides, long-chain                                                                    +
Excipient hypromellose +
Additive titanium dioxide +
excipient macrogol +
Excipient sodium saccharin +
Manufacturer: Woerwag Pharma GmbH & Co. KG

 

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