Rubiefol, 100 pcs

Upute za korištenje Rubiefol, 100 pcs

Important notes (compulsory information):

Rubiefol. Active substance: folic acid. Areas of application: Therapy of folic acid substances that can not be remedied dieting. Warning: This medicine contains lactose.

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


LEAFLET: INFORMATION FOR THE USER

Rubief
Tablets to take / 5 mg
Active substance: folic acid

Dear patient, dear patient!
Please read the following useful information because it contains important information about what you should consider when using this medicine. For questions, please contact your doctor or pharmacist.

Composition:
Pharmacically effective component: Folic acid 1 tablet contains 5.0 MG folic acid.
Other Ingredients: Lactose 1 H2O, Talcum, Cellulose Powder, Hochdiserses Silica Dioxide, Magnesium Stearate

Dosage form and content:
Rubiefol is packed with 20 tablets (NI), 50 tablets (N2) and 100 tablets (N3) available.

Cloth or indicator group:
Vitamins

Pharmaceutic entrepreneur:
RubiePharm Vertriebs GmbH
Brothers Grimm Road 121
30396 Steinau on the street
Tel.: (06663) 9604-0
Fax: (06663) 9604-32
E-mail: [email protected]

Manufacturer:
Artesan Pharma GmbH & Co. KG
Wendlandstr. 1
29439 Lüchow

Application areas:
Therapy of folic acid substances that can not be remedied dieting.

Contraindications:
When should not you use Rubiefol tablets?
The folic acid caused increase in young red blood cells (reticulocytes) can mask a vitamin B12 deficiency. Due to the risk of irreversible neurological disorders, before the therapy of a bloodlessness, as a result of a trusted development of the red blood cells (megaloblast anemia), it is not based on a vitamin B12 deficiency. The cause of a megaloblast anemia must be clarified before the beginning of the therapy.

What do you need in pregnancy and lactation?
There are no risks known.

Precautions for the application and warnings:
What precautions should be taken?
Even with life-threatening megaloblast anemia, a possible vitamin B12 deficiency must be excluded because of the danger of permanent damage of the nervous system before the start of therapy (Ensuring serum and erythrocyte samples and determination of the vitamin B12 content). Rubiefol must not be taken if they are hypersensitive (allergic) against folic acid or any of the other ingredients of Rubiefol.

Important information about certain other ingredients of Rubiefol:
This medicine contains lactose. Please accept Rubiefol only after consulting with your doctor if you are familiar with any intolerance to certain sugars.

Interactions with other means:
Which other medicines influence the effect of Rubiefol tablets?
The administration of folic acid can reduce the blood levels of resources against seizure disorders (anticonvulsants, e.g. phenytoin, phenobarbital, primidone) and thereby u. U. increase the variety. At administration of high doses can not be ruled out that Rubiefol and simultaneously administered females of folic acid (Folic acid antagonists), e.g. Certain drugs against bacterial infections or malaria (trimethoprim, proguanil, pyrimethamine) and methotrexate (active ingredient and a. A. For the treatment of tumors), inhibit mutually in their effect. With simultaneous use with fluorouracil (medicines for the treatment of tumors), severe diarrhea can occur. Chloramphenicol (Drug for the treatment of infections) can prevent response to treatment with Rubiefol and should therefore not be administered to patients with severe folic acid levels.

Dosage instructions, type and duration of the application:
The following information applies as far as your doctor Rubiefol tablets did not prescribe otherwise. Please stick to the application regulations, as Rubiefol tablets otherwise can not act properly!
> How much Rubief tablets should you take and how often?
Depending on requirements 1 to 3 tablets Rubiefol per day (corresponding to 5 - 15 mg folic acid). The tablets are unadarved to the meals with a little fluid.

How long should you apply Rubiefol tablets?
The duration of treatment depends on the extent of the folic acid interface and depends on the clinical image and, if applicable, according to the corresponding laboratory diagnostic measured variables and is determined by the doctor for each patient.

Overdose and other application errors:
What to do if Rubiefol has been used in too large quantities (intended or accidental overdose)?
With occasional higher dosage, no overdose phenomena are expected. However, in patients with disappointment, it can lead to an increase in convulsiveness. At high doses (over 15 mg per day and more than 4 weeks), gastrointestinal disorders, sleep disorders, excitement and depression can occur. In these cases, you should contact your doctor.

Side effects:
Which side effects can occur when using Rubiefol tablets?
In individual cases, surpassification reactions, e.g. in the form of skin soldering (erythema), itching (pruritus), air groove (Bronchospasm), nausea or circulatory collapse (anaphylactic shock) occur. At very high dosages, there may be gastrointestinal disorders, sleep disorders, excitement or depression. If you are watching side effects that are not listed in this leaflet, please tell your doctor or pharmacist.

Which countermeasures are to take with side effects?
Please inform your doctor about the side effects that can be used to treat it in a targeted manner.

Notes and information on the durability of the medicinal product:
The expiration date of this medicine is on the container (Blister) and outer wrapping of Rubiefol tablets printed. Do not use this medicine after this date!

How is Rubiefol to keep?
Store protected from light and moisture. Keep the medicine so that it is not accessible to children.

This information information was last revised in May 2013.

Source: Information of the leaflet
Status: 02/2016