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Fluorine Vigantoletten 500 I.E. Tablets, 90 pcs

Fluorine Vigantoletten 500 I.E. Tablets, 90 pcs

Preventive treatment of caries and rachitis in infants, children in the first two years of life and children with a morbid, insufficient food intake in the intestine.

Manufacturers: Merck Selbstmedikation GmbH

PZN: 01909250

Dosage: Tabletten

Content: 90 St

Reward Points: 47

Availability: Out of stock

$15.92

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Fluorine Vigantoletten 500 I.E. Tablets, 90 pcs

Instructions for use for Fluorine Vigantoletten 500 I.E. Tablets, 90 pcs

Instructions for use for: Fluor- Vigantoletten 500 I.E. Tablets, 90 pcs

Important notes (compulsory information):

Fluorine Vigantoletten 500 I.E. Tablets
. Application areas: Preventive treatment of caries and rickets at infants, children in the first two years of life and children with a morbid, insufficient food intake in the intestine (malabsorption), When the fluoride concentration in drinking water / mineral water under 0.3 mg / l.

For risks and side effects, read the package leaflet and ask your doctor or pharmacist.


Important notes (compulsory information):

Fluorine Vigantoletten 500 I.E. Tablets.
Applications: Preventive treatment of caries and rickets at infants, children in the first two years of life and children with a morbid, insufficient food intake in the intestine (malabsorption), When the fluoride concentration in drinking water / mineral water under 0.3 mg / l.

For risks and side effects, read the package leaflet and ask your doctor or pharmacist.


LEAFLET: INFORMATION FOR THE USER

Fluorine Vigantoletten 500 I.e. Tablets, for use in infants and children
Active ingredients: colecalciferol and sodium fluoride

Read the entire leaflet carefully because it contains important information for you. This medicine is available without prescription. In order to achieve the best possible treatment success, fluorine Vigantoletten 500 I.E. however, be taken correctly.
  • Lift the package leaflet. You might want to read it again.
  • Ask your pharmacist if you need more information or advice.
  • If your complaints worse or no improvement occurs, you must definitely visit a doctor.
  • If one of the listed side effects you significantly affect it or notice side effects that are not specified in this information information, please inform your doctor or pharmacist.


This leaflet contains:
  1. What is Fluoro Vigantolets 500 I.e. And what is it used for?
  2. What do you need before taking fluoro vigantolets 500 I.e. Note?
  3. How is Fluor Vigantolets 500 I.E. take?
  4. WHAT SIDE EFFECTS ARE POSSIBLE?
  5. What is Fluor Vigantolets 500 I.E. Keep?
  6. ADDITIONAL INFORMATION


1. What is Fluoro Vigantolets 500 I.e. And what is it used for?

Previous remedy against caries and rickets. Preventive treatment of caries and rachitis in infants, children in the first two years of life and children with a morbid, insufficient food intake in the intestine (malabsorption) when the fluoride concentration in drinking water / mineral water is below 0.3 mg / l. Explanations: The caries is a common disease of dental tissue (enamel, dentin). In vitamin D deficiency of rickets (so-called English disease), the bones can not be formed sufficiently firmly. The vitamin D recorded with the food must be converted into vitamin D3 in the body, which happens in the skin by sunshine. The illness therefore occurred especially in England. For children with an insufficient food intake from the intestine, too little vitamin D is also added. In both cases, the disease is bent through the administration of vitamin D3.

2. What you need before taking fluorine vigantolets 500 I.E. NOTE?

Fluorine Vigantoletten 500 I.E. may not be taken:
  • if you hypersensitive (allergic) against the active ingredients, soy, peanut or any of the other ingredients of fluorine Vigantoletten 500 I. E. are,
  • when the calcium in the blood (hypercalcaemia) or in urine (Hypercalcurie) is increased,
  • with limited mobility (e.g., because of a plaster association) or
  • if a different type of fluorides are supplied, e.g. with drinking, mineralthe table water.


Special care when taking fluorine Vigantoletten 500 I.e. is required:
  • when a systemic fluoride feed takes place. For example, children under 3 years should not use fluoride-containing tooth pastes.
  • when infants are fed with recorded diets or when their bottle food is made with drinking or mineral water containing over 0.3 mg fluoride per liter. In this case, an additional fluoride supply (e.g., by fluoride tablets) is not recommended.
  • when children receive an accounted diet because of a congenital metabolic disorder. In this case, the administration of fluoride tablets is not required.
  • in severe, long-term diseases impaired. In this case is to be weighed on your doctor if Fluor- Vigantoletten 500 I.e. can be given.
  • in early and deficiency infants. Here, the caries prophylaxis should only be used by systemic fluoride supply after reaching a body weight of 3000 g and normal physical development.
  • when milk enriched with vitamin D3 is used. In this case, the addition of vitamin D3 may not be required.
  • when there is a sarcoidosis, since the risk of reinforced conversion of vitamin D is in its active form. In this case, the calcium levels in the blood and urine should be monitored.
  • for inclination to form calcium-containing kidney stones.


In patients with impaired renal function, with fluorine Vigantoletten 500 I.E. Treated, the effect on the calcium and phosphate budget should be monitored. If other vitamin D-containing drugs are prescribed, the dose of vitamin D of Fluor- Vigantoletten 500 I.e. Be taken into account. Additional administrations of vitamin D or calcium should only take place under medical supervision. In such cases, the calcium levels must be monitored in the blood and urine. Fluorine Vigantoletten 500 I.E. If infants and toddlers are particularly careful, as they may not be able to swallow the tablets. It is recommended to resolve the tablets as indicated instead.

When taking fluorine Vigantoletten 500 I.E. With other medicines:
Please inform your doctor or pharmacist if you take / use other medicines or recently taken / applied, even if it is non-prescription medicines. Phenytoin (Medicines for the treatment of epilepsy) or barbiturates (Medicines for the treatment of epilepsy and sleep disorders as well as for anesthesia) can affect the effect of vitamin D. Thiazid-Diuretics (medicinal products for promoting urinary excretion) can result in hypercalcaemia (increased calcium concentration in the blood) by reducing the calcium excretion over the kidney. The calcium levels in the blood and in the urine should therefore be monitored during a long-term treatment. Simultaneous administration of glucocorticoids (medicines for the treatment of certain allergic diseases) may affect the effect of vitamin D. Vitamin D Metabolites or Analoga (e.g. Calcitriol): a combination with fluorine Vigantoletten 500 I.E. Only recommended in exceptional cases. The calcium levels in the blood should be monitored.

Rifampicin and Isoniazide (medicines for the treatment of tuberculosis):
The metabolism of vitamin D can be increased and the effectiveness can be reduced. The risk of an undesirable effect in taking heart glycosides (medicinal products for promoting the function of the heart muscles) may increase as a result of increasing the calcium levels in the blood during treatment with vitamin D (risk for cardiac arrhythmias). Patients should be monitored in the blood and urine in terms of ECG and calcium levels and, if necessary, in terms of medication levels in the blood. Please note that this information can also apply to recently used medicines. With an additional application of fluoride-containing gels or paints, the doctor or dentist should be questioned.

When taking fluorine-Vigantoletten 500 I.e. Together with food and beverages:
A simultaneous supply of calcium and magnesium, as it takes place during a diet with milk and dairy products, can reduce the absorption of fluoride.

Pregnancy and breast feeding period:
Ask your doctor or pharmacist for advice before taking / application of all medicines. This medicine is intended only for use in infants and children. Pregnant and breastfeeding women may fluorine Vigantoletten 500 I.e. Do not take.

Driveion and use of machines:
Not applicable.

Important information about certain other ingredients of fluorine Vigantoletten 500 I.E.:
This medicine contains sucrose. Please use fluorine Vigantoletten 500 I.e. Only after consultation with your doctor, if you know that your child suffers from intolerance to certain sugars.

3. What is Fluor Vigantolets 500 I.e. take?

Take Fluor- Vigantoletten 500 I.E. Always close exactly after the physician's instruction. Please ask your doctor or pharmacist if you are not sure. Unless otherwise prescribed by the doctor, the usual dose is: The dosage is dependent on the age of the child and should be determined under consideration of other fluoride recording. In order to ensure that only a systemic form of fluoride supply is used, the pediatrician should take into account the intake of fluoridated dining salt, fluoride tablets (including the daily dose), fluoride-rich mineral water and the fluoride content of the drinking water at the dosage recommendation. The following dosing recommendations apply to fluoride concentrations in the drinking or mineral water of less than 0.3 mg fluoride per liter. Infants and toddlers up to 2 years receive 1 tablet fluorine Vigantoletten 500 I.E. Children with insufficient food intake in the intestinal (malabsorption) receive from the 3rd to the 6th year for preventive treatment daily 2 tablets fluorine Vigantoletten 500 I.E. If the fluoride concentration in drinking water / mineral water is more than 0.7 mg / l, an additional administration of fluoride-containing tablets is not displayed.

Type of application:
The tablet (s) is decayed on a teaspoon in water and then for better utilizing the local fluoride effects have some time in the mouth (if possible). The best time of application is in the evening after brushing teeth, since the high fluoride concentrations on the teeth are retained longer. When the crushed fluorine Vigantoletten 500 I.E. To a bottle or mucurement for infants, pay attention to complete consumption, otherwise not the total amount of active ingredient is supplied. The addition should only be cooked after cooking and then cooling.

Duration of application:
Apply Fluor- Vigantoletten 500 I.E. without medical or dental advice no longer than 365 days. The doctor decides on the duration of the treatment. If only insufficient amounts of fluoride and vitamin D are included with the food in duration, fluorine Vigantoletten 500 I.e. to be taken by the end of the second year of life. Please talk to your doctor or pharmacist if you have the impression that the effect of fluorine Vigantoletten 500 I.e. too strong or too weak.

If you have a larger amount of fluoro Vigantoletten 500 I.E. have taken than you should:
With unique overdose, no side effects are expected. In acute recording very high doses, gastrointestinal malfunctions such as nausea, abdominal pain and diarrhea can occur. In such a case, contact your doctor immediately. An acute overdose is absolutely to avoid (Passing poisoning). With chronic overdose of fluoride in the first years of life, a dental fluorosis with melt defects can develop at the lasting denture. In isolated fluoride overdose is the treatment with fluorine Vigantoletten to end. Long-term overdose of vitamin D can lead to hypercalcemia (increased calcium concentration in the blood) and hypercalcuria (increased calcium concentration in urine). With significant and long continuous exceeding of the needs can lead to calcification of vessels and organs. The first measure is to set the preparation and to add plenty of fluid. Complaints may require an increase in urinary excretion and the administration of glucocorticoids (medicines for the treatment of certain allergic diseases) and calcitonin (hormone to control calcium concentration in the blood). A special antidote does not exist.

If you are taking fluorine Vigantoletten 500 I.e. Forgot:
Do not take the double dose if you forget the previous ingestion. Once became a tablet fluorine Vigantoletten 500 I.E. Forgot, the administration will be continued unchanged. Became fluorine Vigantoletten 500 I.E. not given over several weeks, then the administration can be extended by the corresponding period of time after consultation with your doctor.

If you are taking fluorine Vigantoletten 500 I.E. abort:
Ask your doctor or pharmacist if you are taking fluorine Vigantoletten 500 I.e. Cancel.

If you have further questions about the application of the medicine, ask your doctor or pharmacist.

4. Which side effects are possible?

Like all medicines, Fluor- Vigantoletten 500 I.E. Have side effects, which do not have to occur with everyone. If you observe side effects with your child, please tell your doctor or pharmacist. The frequencies of the side effects are unknown because no major clinical trials have been carried out which allow an estimation of frequencies.

Possible side effects:
Metabolic and nutritional disorders:
Hypercalcemia (increased calcium concentration in the blood) and hypercalcuria (increased calcium concentration in urine).

Diseases of the gastrointestinal tract:
Complaints in the gastrointestinal tract such as constipation, bloating, nausea, abdominal pain or diarrhea.

Diseases of the skin and subcutaneous tissue:
Hypersensitivity reactions such as itching, rash or hives.

Other possible side effects:
Soyl oil can rarely cause allergic reactions.

Please inform your doctor or pharmacist if one of the listed side effects will significantly affect it or notice side effects that are not specified in this document formation.

5. What is Fluor Vigantolets 500 I.e. Keep?

Store drug out of reach of children. You may not use the medicinal product after the expiry date specified on the carton. The expiry date refers to the last day of the month. Storage conditions: Do not store more than 25 ° C. Store in the original packaging to protect the content from light. The tablets are to be removed until the blister immediately before use. Note on durability after breaking or preparation: Not applicable. The medicine must not be disposed of in wastewater or budgetary waste. Ask your pharmacist how to dispose of the medicine if you no longer need it. This measure helps protect the environment.

6. Further information

What fluorine Vigantoletten 500 I.e. Contains:
The active ingredients are: colecalciferol and sodium fluoride. 1 tablet Fluor- Vigantoletten 500 I.E. Contains 5.0 mg colecalciferol dry concentrate (corresponding to 500 I.e. Vitamin D3) and 0.55 mg of sodium fluoride (corresponding to 0.25 mg of fluoride). The other ingredients are: high-disperses silica, corn starch, poly (O-carboxymethyl) starch, sodium salt, talc, glyceroltridodecanoate, cellulose, mannitol (pH. EUR.), Gelatin, sucrose (sucrose), soybean oil (pH . EUR.), All-rac alpha-tocopherol.

Like fluorine Vigantoletten 500 I.E. Tablets appearance and content of the pack:
White round tablet with jewelry groove and embossing EM 62 on the top. Pack of 30 tablets and pack with 90 Tablets.

Pharmaceutical entrepreneur and manufacturer:
Pharmaceutic entrepreneur:
Merck Serono GmbH
As wheels road 17
64289 Darmstadt
E-Mail: medical [email protected]
Service number (6 cents per interview from the network of telecom, if necessary Different prices from the mobile network):
Tel.-No.: 0180 222 7600
fax-No.: (0 61 51) 6285-816

Department:
Merck Selbstmedikation GmbH
Frankfurter Straße 250
64293 Darmstadt
Tel.: 06151-856 2323
E-Mail: [email protected]

Manufacturer
Merck KGaa & Co. Werk Spittal
Hösslgasse 20
9800 Spittal / Drau
Austria

This information information was last revised in June 2014.

Source: Information of the leaflet
Status: 03/2017

For risks and side effects, read the package leaflet and ask your doctor or pharmacist.

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