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Folverlan 0.4 mg tablets

Folverlan 0.4 mg tablets

AED 102.00
+ AED 46.00 Air Shipping

  • Includes any applicable VAT and customs duty.
  • Air shipping cost to be recalculated with delivery address at checkout.
  • To be delivered in 6 - 9 * working days.
  • 100% genuine and new product.
  • Credit card / Cash on Delivery
Description

Folverlan 0.4 mg tablets
Provider: Verla-Pharm Arzneimittel GmbH & Co. KG
Daring form: tablets
20 st | PZN: 01032930
50 st | PZN: 01032953
100 st | PZN: 01032982
active ingredient: folic acid-x water
Read the package supplement and ask your doctor or pharmacist.
Important information (mandatory information):
Folverlan 0.4 mg.
active ingredient: folic acid. Areas of application: prevention of neural tube defects, in particular the spina bifida ("open back"), prevention and treatment of folic acid deficiencies that cannot be remedied dietetically.
Use information: Information for the user
Folverlan 0.4 mg
tablets
active ingredient: folic acid
Read the entire package insert carefully because it contains important information for you. This medicine is available without a prescription. In order to achieve the best possible treatment success, Folverlan 0.4 mg must be used in accordance with prescription.
- Use the package insert. You might want to read it again.
- Ask your doctor or pharmacist if you need more information or advice.
- If your symptoms worsen or no improvement occurs after several weeks, you will definitely have to see a doctor.
- If one of the side effects listed significantly impairs you or you notice side effects that are not specified in this package insert, please inform your doctor or pharmacist.
This package insert contains:
1. What is Folverlan 0.4 mg and what is it used for?
2. What do you need to consider before taking Folverlan 0.4 mg?
3. How can Folverlan be taken 0.4 mg?
4. What side effects are possible?
5. How is Folverlan 0.4 mg to be kept?
6. Further information
1. What is Folverlan 0.4 mg and what is it used for?
Folverlan 0.4 mg is a vitamin preparation.
Folverlan 0.4 mg is used
- to prevent neural tube defects, in particular the spina bifida ("open back"),
- for the prevention and treatment of folic acid false, which cannot be remedied dietetically.
2. What do you need to consider before taking Folverlan 0.4 mg?
Folverlan 0.4 mg must not be taken
- if they are hypersensitive (allergic) against folic acid or one of the other components of foltlan 0.4 mg,
- if there is anemia that is on a vitamin B12 deficiency is based.
The increase in young red blood cells (reticulocytes) caused by folic acid gear can cover a vitamin B12 deficiency. Due to the risk of permanent damage to the nervous system, anemia must be ensured before anemia due to disturbed development of red blood cells (megaloblast anemia) that it is not based on a vitamin B12 deficiency. The cause of a megaloblast anemia must be clarified before the start of treatment.
special caution when taking Folverlan 0.4 mg is required if you have determined a so-called megaloblast anemia (a form of anemia) (see above), which is based on the sole lack of vitamin B12 (z B. due to the lack of the so-called intrinsic factor, which is necessary for the absorption of vitamin B12) or the cause of which is not to be clarified. In this case, please follow your doctor's advice. Even in the event of life-threatening megaloblast anemia, a possible vitamin B12 deficiency must be excluded due to the risk of permanent damage to the nervous system before the start of treatment (ensuring serum and erythrocyte samples and determination of the vitamin B12 content).
When taking Folverlan 0.4 mg with other medicinal products:
Please inform your doctor or pharmacist if you have used other medicines or have recently applied, even if it is not prescription drugs. The effect below can be influenced below with Folverlan 0.4 mg. Under the treatment with funds against seizure disorders (anticonvulsant), there may be an increase in willingness to seize. With the gift of high doses, it cannot be ruled out that Folverlan 0.4 mg and at the same time administered inhibitors of folic acid (folic acid antagonists), such as: B. certain drugs against bacterial infections or malaria (trimethoprim, proguanil, pyrimethamine) and methotrexate (active ingredient, etc. for the treatment of tumors), inhibit each other. With simultaneous use with fluorouracil (medium to treat tumors), serious diarrhea can occur. Chloramphenicol (active ingredient for the treatment of infections) can prevent response to treatment with Folverlan 0.4 mg and should therefore not be administered to patients with severe folic acid deficiency symptoms. Please note that this information can also apply to recently applied medicines.
pregnancy and lactation:
Folverlan 0.4 mg can be taken during pregnancy and breastfeeding. No risks are known. A prenatal diagnosis on neural tube defects (childlike malformations) is also necessary under the preventive intake of Folverlan 0.4 mg.
traffic and operating machines:
No special precautionary measures are required.
Important information about certain other components of Folverlan 0.4 mg:
This medicine contains lactose (milk sugar). Please only take Folverlan 0.4 mg after consulting your doctor if you are aware that you suffer from intolerance to certain sugar. In the case of lactose intolerance due to Lactasm deficiency, the small amount of lactose (39.5 mg per tablet) most likely does not cause any symptoms.
3. How can Folverlan be taken 0.4 mg? Always take Folverlan 0.4 mg exactly after instruction in this package insert. Please ask your doctor or pharmacist if you are not quite sure.
Dosage
If the doctor is not prescribed otherwise, the usual dose is:
to prevent neural tube defects: 1 tablet daily (corresponding to 0.4 mg folic acid daily).
For the prevention of folic acid deficits: 1 to 2 tablets daily (corresponding to 0.4 mg to 0.8 mg folic acid daily).
For the treatment of folic acid deficiencies: 3 x 2 to 3 x 4 tablets daily (corresponding to approx. 2.5 mg to 5 mg folic acid daily).
Type of application
The tablets are taken with some liquid with some meals. There is no special recommendation for the respective point in time.
The doctor decides on the duration of the application. Unless otherwise prescribed, it is recommended:
to prevent neural tube defects in women with existing children's desire: to ensure sufficient folic acid body stock, at the beginning of pregnancy, but better one month before the occurrence of folklan 0.4 MG be started. However, since pregnancy is often not predictable, all women are recommended to take Folverlan 0.4 mg regularly as long as the possibility of pregnant shaft cannot be ruled out. Treatment should be continued at least up to three months after pregnancy. A possibly longer application of Folverlan 0.4 mg before and/or after the occurrence of pregnancy is harmless.
For the prevention of folic acid deficits: The duration of use depends on the respective circumstances that require a supplement to folic acid requirement. There is no temporal restriction of the duration of use, even the long -term intake of Folverlan 0.4 mg is harmless in the recommended dosage.
for the treatment of folic acid deficits: The duration of the treatment depends on the extent of the folic acid lack and depends on the clinical image and, if necessary, according to the corresponding laboratory diagnostic measurement variables. It is determined by the doctor for each patient. If Folverlan was prescribed 0.4 mg, you should only cancel the treatment after consultation with your doctor.
Please speak to your doctor or pharmacist if you have the impression that the effect of Folverlan 0.4 mg is too strong or too weak.
If you have taken a larger amount of folklan 0.4 mg than you should:
- with occasional higher dosage, no overdose signs can be expected.
- In patients with seizures, however, there can be an increase in willingness to seize.
-With very high doses (over 15 mg per day and longer than 4 weeks), gastrointestinal disorders, sleep disorders, excitement and depression can occur.
In these cases you should contact your doctor.
If you have forgotten the intake of Folverlan 0.4 mg:
Do not take the double dose if you have forgotten the prior intake. If you have any further questions about the application of the drug, ask your doctor or pharmacist.
4. What side effects are possible?
Like all medicines, Folverlan can have 0.4 mg side effects, but which do not have to occur with everyone.
The following frequency information is used when evaluating side effects:
very often:
more than 1 treated of 10
frequently:
1 to 10 treated by 100
occasionally:
1 to 10 treated by 1
rare:
1 to 10 of 10,000
Dear:
less than 1 treated of 10,000
Not known:
Frequency based the available data cannot be estimated.
In individual cases, hypersensitivity recovery campaigns e.g. B. in the form of reddening of the skin (erythema), itching, breathing shortage (bronchospasm), nausea or circulatory collapse (anaphylactic shock). Rarely can gastrointestinal disorders, sleep disorders, excitement and depression occur with very high doses (over 15 mg per day and longer than 4 weeks). Please inform your doctor or pharmacist if one of the side effects listed is significantly impaired or you notice side effects that are not specified in this package insert.
5. How is Folverlan 0.4 mg to be kept?
Keep drugs for children inaccessible.
You can no longer use the medicine after the expiry date specified on the folding box and the pressure pack.
storage conditions:
dry and not over 25 ° C!
Store in the original packaging to protect the content from moisture.
6. Further information
What Folverlan contains 0.4 mg:
The active ingredient is: folic acid
1 tablet contains 0.4 mg folic acid.
The other ingredients are: pre-clerk strength, lactose monohydrate, poly (o-carboxymethyl) strength sodium salt, microcrystalline cellulose, high-disperses silicon dioxide, magnesium stearate (ph.).
FOLFLAN 0.4 mg does not contain any gluten.
what Folverlan looks 0.4 mg and contents of the pack:
It is small, round tablets with longitudinal prompt and pale yellow color. Folverlan 0.4 mg is available in packs with 20 (N1), 50 (N2) and 100 (N3) tablets.
Pharmaceutical entrepreneur and manufacturer:
Verla-Pharm Arzneimittel GmbH & Co.KG,
82324 Tutzing,
www.verla.de.
This use information was last revised in September 2010.
Source: www.verla.de
Stand: 07/2014
Manufactured by: Verla-Pharm Arzneimittel GmbH & Co. KG
Br>-prevention of a neural tube defect in newborns-prevention of folic acid defects-Therapy of folic acid deficits
Composition
Folic acid-X-water, folic acid, strength, pre-mutilated, lactose 1 water, lactose, carboxymethylarie, sodium, cellulosis, microcranosis , Silicium dioxide, high -disperses, magnesium stair (vegetable)
dosage
tablets
Application notes
The total dose should not be exceeded without consultation with a doctor or pharmacist.
Type of application?
Take in the medicine with liquid (e.g. 1 glass of water).
duration of the application?
The duration of use depends on the type of complaint and/or duration of the disease and is therefore only determined by your doctor.
overdosing?
In the case of an overdose, there can be a bitter taste, loss of appetite, nausea, bloating, nightmares, excitement and depression. If you suspect an overdose, contact a doctor immediately. The following applies
: Pay particular attention to a conscientious dosage in infants, toddlers and older people. If in doubt, ask your doctor or pharmacist about any effects or precautionary measures.
A dosage prescribed by the doctor may differ from the information on the package insert. Since the doctor coordinates you individually, you should therefore apply the medicine according to his instructions.
Contraindications
What speaks against an application?
- hypersensitivity to the ingredients
- anemia with enlarged red blood cells (hyperchrome anemia)
What about pregnancy and breastfeeding?
- pregnancy: contact your doctor. Different considerations play a role in whether and how the medicine can be used during pregnancy.
- breastfeeding: contact your doctor or pharmacist. He will check your special starting position and advise you accordingly whether and how you can continue with breastfeeding.
If you have been prescribed the medicine despite a counter -notification, speak to your doctor or pharmacist. The therapeutic benefit can be higher than the risk of using a counter -notification.
Side effects
What undesirable effects can occur?
- Allergic reaction
- Inflammatory skin reddening (erythema)
- itching (pruritus)
- cramp of the bronchi
- nausea
- circulatory failure by an allergic reaction (anaphylactic shock)
- Sleep disorders
- arousal
- Depression
- Disorder in the gastrointestinal tract
If you notice a disorder or change during treatment, contact your doctor or pharmacist.
For information at this point, side effects are taken into account that occurs in at least one of 1,000 patients treated.
Important information
What should you consider?
caution in the event of intolerance to lactose. If you have to adhere to a diabetes diet, you should take the sugar content into account.
package insert
package insert

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Folverlan 0.4 mg tablets

AED 102.00
+ AED 46.00 Air Shipping

  • Includes any applicable VAT and customs duty.
  • Air shipping cost to be recalculated with delivery address at checkout.
  • To be delivered in 6 - 9 * working days.
  • 100% genuine and new product.
  • Credit card / Cash on Delivery
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