JASIVENTER 500 mg lozenges, 20 pcs

Instructions for use for JASIVENTER 500 mg lozenges, 20 pcs

Application instructions

Young people aged 12 and over and adults

1-2 Chewable tablets

1-6 times daily

when symptoms occur, between meals and before going to bed

Application areas

Mode of action

How does the ingredient of the medicine work?

The active ingredient binds and neutralizes stomach acid. The aluminum and magnesium contained in the compound form poorly soluble salts with stomach acid, which are excreted through the stool. In this way it is effective against heartburn, belching and other acid-related stomach problems. In addition, the risk of ulcers occurring in the gastrointestinal area as a result of hyperacidity is reduced.

Composition

Contraindications

What speaks against an application?

Always:
- Hypersensitivity to the ingredients
- Phosphate deficiency

Under certain circumstances - talk to your doctor or pharmacist about this:
- Impaired kidney function

Which age group should be taken into account?
- Children under 12 years: The medicine should generally not be used in this age group.

What about pregnancy and lactation?
- Pregnancy: Consult your doctor. Various considerations play a role in whether and how the medicine can be used during pregnancy.
- Breast-feeding: According to current knowledge, there is no evidence that the medicine should not be used during breast-feeding.

If you have been prescribed this medicine despite a contraindication, talk to your doctor or pharmacist. The therapeutic benefit may be greater than the risk associated with use if there is a contraindication.

Side effects

What adverse effects may occur?

The following can occur, especially with long-term use of high doses:
- Gastrointestinal complaints such as:
- Soft stools
- Diarrhea
- Increased magnesium levels
- Increased aluminum levels
- Phosphate deficiency

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

The information provided here primarily takes into account side effects that occur in at least one in 1,000 treated patients.

Hints

What should you pay attention to?
- The medicine may mask symptoms that indicate a serious illness. Therefore, if you have any long-lasting symptoms, please consult your doctor before taking the medication.
- Be careful if you are allergic to the sweetener saccharin (E number E 954)!
- Be careful if you are allergic to the sweetener cyclamate (E number E 952)!
- Be careful if you have an intolerance to fructose (fruit sugar). If you have to follow a diabetes diet, you should consider the sugar content.
- There may be medicines that interact with. You should therefore generally tell your doctor or pharmacist before starting treatment with a new medicine that you are already using. This also applies to medicines that you buy yourself, only use occasionally or that were used some time ago.
- Lemonade, orange juice, lemon juice, fruit juice, wine and citric acid (e.g. as an excipient in effervescent tablets) must not be taken together with the medication.

Detailed instructions for JASIVENTER 500 mg lozenges, 20 pcs

Field of use

• These chewable tablets are antacids. These are agents that bind excess stomach acid. They are used for the symptomatic treatment of diseases in which stomach acid needs to be bound:
  • Stomach and duodenal ulcers (ulcus ventriculi and ulcer duodenal)
  • Heartburn and acid-related stomach problems

Active ingredients / ingredients / ingredients

500 mg hydrotalcite
Arabic gum excipient (+)
Levomenthol excipient (+)
Maltitol excipient (+)
Maltodextrin excipient (+)
Sodium cyclamate excipient (+)
Paraffin, low-viscosity excipient (+)
Peppermint oil excipient (+)
Saccharin, sodium salt excipient (+)
Titanium dioxide auxiliary (+)
Wax, bleached auxiliary (+)
Water, purified excipient (+)
Xanthan gum excipient (+)
0.07 BE Total carbohydrate excipient (+)

Contraindications

• The preparation must not be taken,
  • if you are allergic to hydrotalcite, menthol or any of the other ingredients of this medicine;
  • if you suffer from severe kidney dysfunction.
• If your kidney function is impaired, you have an increased risk of increased accumulation of magnesium and aluminum in the blood if you take high doses of this medicine over the long term. In the long term, increased accumulation of aluminum can lead to painful bone softening (osteomalacia) or pathological, non-inflammatory brain changes (encephalopathy). Therefore, if you have impaired kidney function, you may only use the medicine if the serum levels of magnesium and aluminum are regularly checked by a doctor. An aluminum level of 40 µg/l should not be exceeded.
• If you have e.g. If, for example, you have a phosphate deficiency (hypophosphatemia) due to a low-phosphate diet or you suffer from pathological muscle weakness or fatigue (myasthenia gravis), you should not take the preparation.

dosage

• Always take this medicine exactly as described or exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are unsure.
• Unless otherwise prescribed by the doctor, adults and children over 12 years of age take 1 - 2 chewable tablets (equivalent to 500 - 1000 mg hydrotalcite) several times a day between meals and before going to bed if necessary.
• The daily dose should not exceed 12 chewable tablets, equivalent to 6000 mg hydrotalcite.
• Other medicines should generally be taken one to two hours before or after taking these chewable tablets.
• Use in children and adolescents
  • The medicine should not be used to treat children under 12 years of age as there is insufficient experience in this age group.

• Duration of application
  • The duration of treatment depends on the type and severity as well as the course of the disease.
  • If the symptoms persist for longer than 2 weeks during treatment, you should consult a doctor.
• 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 have taken more than you should
  • Poisoning is unlikely due to the low absorption of aluminum and magnesium.
  • 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.

 

• If you forget to take it
  • Do not take a double dose if you forget to take the previous dose. Continue treatment at the prescribed dose.

 

• If you stop taking it
  • Be sure to talk to your doctor before - e.g. B. due to the occurrence of side effects - interrupt the treatment or end it prematurely.

 

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

Intake

• If necessary, take several times a day between meals and before bed
• Other medicines should generally be taken one to two hours before or after taking the preparation.

Patient information

• Warnings and Precautions
  • Please talk to your doctor or pharmacist before taking the medicine.
    • If your kidney function is impaired, you suffer from Alzheimer's or other forms of dementia, or you are on a low-phosphate diet, you should avoid long-term use of high doses of this medicine.
    • Prolonged and recurring stomach problems can be signs of a serious illness, such as: B. a stomach or duodenal ulcer. Treatment with this medicine should therefore not last longer than 14 days without a medical examination.
    • In patients with gastric or duodenal ulcer, an examination for the gastric bacterium H. pylori - and, if this is detected - a recognized antibacterial therapy should be considered, as the ulcer disease usually heals if such therapy is used successfully.
    • If tarry stools, blood in the stool or vomiting of blood occur, please see a doctor immediately, as these can also be signs of a serious illness.
  • Children and young people
    • The medicine should not be used to treat children under 12 years of age as there is insufficient experience in this age group.

 

• Ability to drive and use machines
  • There are no special precautions required.

Pregnancy

• 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.
• There have been no reports of harmful effects of hydrotalcite during pregnancy or breastfeeding. However, there are no specific studies on children whose mothers took hydrotalcite during pregnancy or breastfeeding.
• Pregnancy
  • The medicine should only be taken during pregnancy after consultation with a doctor and for a short period of time in order to avoid the child being exposed to aluminum. However, there is no risk for the newborn as only very small amounts are absorbed by the child.
• Lactation
  • In general, aluminum compounds pass into breast milk. However, there are no studies on the transfer of hydrotalcite into breast milk.

Hints

Manufacturer:  Bolder Arzneimittel GmbH & Co. K, Rheinische Allee 11