ULTILAC N chewable tablets, 20 pcs

Instructions for use for ULTILAC N chewable tablets, 20 pcs

Field of use

• The preparation is a medicine for the treatment of diseases in which excess stomach acid is to be bound:
  • Heartburn and acid-related stomach problems
  • Stomach and duodenal ulcers (ulcus ventriculi and ulcer duodenal)

Active ingredients / ingredients / ingredients

360 mg almasilate
120 mg calcium carbonate
250 mg dry skimmed milk
Milk
Calcium bisdocosanoate excipient (+)
Carboxymethyl starch, sodium salt excipient (+)
Cellulose, microcrystalline excipient (+)
Magnesium stearate excipient (+)
Povidone K25 excipient (+)
Saccharin, sodium salt excipient (+)
220 mg sorbitol excipient (+)
0.2 BE Total carbohydrate excipient (+)
Starch hydrolyzate excipient (+)
Talc excipient (+)
Caramel flavor excipient (+)

Contraindications

• The medicine must not be taken:
  • if you are hypersensitive (allergic) to almasilate, calcium carbonate, dry skimmed milk or any of the other ingredients of the medicine
  • of patients with hypercalcemia

dosage

• Take the medicine exactly as directed. Please ask your doctor or pharmacist if you are not sure.
• Unless otherwise prescribed by the doctor, the usual dose is:
  • Heartburn and acid-related stomach problems:
    • If necessary, 2 to 3 chewable tablets several times a day
  • Stomach and duodenal ulcers:
    • 2 to 3 chewable tablets 4 to 8 times a day, corresponding to a daily dose of 100 to 200 mVal.

 

• Duration of application
  • The duration of treatment depends on the type and severity of the disease. For stomach and duodenal ulcers, treatment should be continued for at least 4 weeks - even after symptoms have disappeared.
  • Please talk to your doctor or pharmacist if you have the impression that the effect of the medicine is too strong or too weak.

 

• If you take more than you should:
  • In the event of an overdose, changes in stool behavior such as softening of stools and an increase in stool frequency may occur. Therapeutic measures are generally not necessary here.
  • Poisoning from the drug is unlikely due to the low absorption of aluminum and magnesium.

 

• If you forget to take:
  • If you have taken too little or forgotten an application, please do not take any more tablets next time and instead continue treatment with the prescribed dose.

 

• If you stop taking:
  • Before you possibly If, for example, you have to interrupt or prematurely stop treatment with the medicine due to side effects, be sure to talk to your doctor or pharmacist.

Intake

• The chewable tablets should be chewed intensively.
• For stomach and duodenal ulcers, the chewable tablets should be taken one to three hours after meals and before going to bed.

Patient information

• Take special care when taking:
  • if kidney function is impaired, the drug should only be administered with regular monitoring of serum levels of magnesium and aluminum. Serum aluminum levels should not exceed 40 ng/ml.
  • when calcium and alkali intake from other sources (food, fortified foods or other drugs), serum and urine calcium levels should be monitored.
  • This medicine contains sorbitol. Please only take the product after consulting your doctor if you know that you have an intolerance to certain sugars.

 

• Ability to drive and use machines:
  • Taking this medicine does not affect your ability to react, perceive or judge, so that there are no effects on driving a motor vehicle or operating machines

Pregnancy

• Pregnancy
  • The medicine should only be used short-term during pregnancy to avoid exposing the child to aluminum. In animal experiments, the administration of aluminum salts led to harmful effects on the offspring.
• Lactation
  • Aluminum compounds pass into breast milk. Due to the low absorption, no risk for the newborn is assumed.

Hints

Manufacturer:  BITTERMEDIZIN Arzneimittel-Vertr, Waldtruderinger Straße 27c