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MIBE Arzneimittel Decristol 1,000 i.E. tablets

MIBE Arzneimittel

AED 53.00
+ AED 44.00 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

DECRISTOL 1,000 I.E. Tablets
Provider: MIBE GmbH Pharmaceuticals
Daring form: tablets
50 st | PZN: 10068944
100 st | PZN: 10068950
200 st | PZN: 10068967
active ingredient: Colecalciferol dry concentrate
Read the package supplement and ask your doctor or pharmacist.
Important information (mandatory information):
Cystinol acute dragees, excessive tablets.
active ingredient: bear grape blades dry extract. Areas of application: For prevention against rachitis (calcification disorder of the skeleton in the growth age) and osteomalacia (bone deviation) in children and adults, to prevent vitamin D deficiency in children and adults with recognizable risk and for supporting osteoporosis (breakdown of the bone tissue) Adults.
Use information: Information for the user
Dekristol 1000 I.E. Tablets for use in infants, children and adults
active ingredient: Colecalciferol (vitamin D3)
Read the entire package insert beforehand before taking it with the use This drug begins because it contains important information. Always take this medicine exactly as described in this package insert or take exactly according to your doctor or pharmacist.
Use the package insert. You might want to read it again.
Ask your pharmacist if you need more information or advice.
If you notice side effects, contact your doctor or pharmacist. This also applies to side effects that are not specified in this package insert. See section 4.
If you don't feel better or worse, contact your doctor.
What in this package insert:
What is Dekristol 1000 I.E. And what is it used for?
What should you consider before taking decristol 1000 I.E.?
How is Dekristol 1000 I.E. to be taken?
What side effects are possible?
How is Dekristol 1000 I.E. to be kept?
Content of the package and further information
1. What is Dekristol 1000 I.E. And what is it used for?
DEKRISTOL 1000 I.E. contains vitamin D3 (Colecalciferol) to regulate the intake and metabolism of calcium and calcium installation in the bone tissue. DEKRISTOL 1000 I.E. is used to prevent rachitis (calcification disorder of the skeleton in the growth age) and osteomalacia (bone soft deviation) in children and adults, to prevent vitamin D deficiency in children and adults with recognizable risk and to support the treatment of osteoporosis (degradation of the Bone tissue) in adults.
2. What should you consider before taking decristol 1000 I.E.?
Dekristol 1000 I.E. must not be taken:
If you are allergic to Colecalciferol or one of the other components of this drug mentioned in section 6,
If you suffer from hypercalcemia (increased calcium concentration in the blood),
If you have hypercalziuria (increased calcium concentration in urine),
if you diagnose hypervitaminosis D (high vitamin D concentrations in the blood),
if you have kidney stones.
Warnings and precautionary measures:
Please speak to your doctor or pharmacist before you take 1000 I.E.
Special caution when taking Dekristol 1000 I.E. is required:
if you tend to form calcium -containing kidney stones.
If you have a disturbed excretion of calcium and phosphate about the kidney.
if they are treated with medicines to promote urine excretion (benzothiadiazin derivatives).
If your movement ability is severely restricted, since in this case there is the risk of hypercalcemia (increased calcium concentration in the blood) and hypercalziuria (increased calcium concentration in urine).
If you suffer from sarcoidosis (a specific disease that attacks the connective tissue in the lungs, skin and joints), since the risk of increased conversion of vitamin D into its active shape. In this case, the calcium levels in the blood and urine should be monitored for you.
If your parathormone household is disrupted (pseudohypoparathyroidism), since the vitamin D requirement can be reduced by the phases of normal vitamin D sensitivity. Then there is a risk of long overdose. For this purpose, more controllable active ingredients with vitamin D activity are available.
If your kidney function is disturbed and you are treated with DEKRISTOL 1000 I.E., your doctor should monitor the effect of treatment on the calcium and phosphate balance. If other vitamin D-containing medicines are prescribed, the dose of Vitamin D of Dekristol 1000 i.E. must be taken into account. Additional administration of vitamin D or calcium should only be carried out under medical monitoring. In such cases, the calcium levels in the blood and urine must be monitored.
Infants and toddlers:
DEKRISTOL 1000 I.E. should only be used with special caution in infants and toddlers, since these may not be able to swallow the tablets. It is recommended to dissolve the tablets as stated instead (see section 3 "How is Dekristol 1000 I.E. to be used?") Or drops.
daily doses over 500 I.E.:
During long -term treatment with DEKRISTOL 1000 I.E. The calcium levels in the blood and urine should be monitored every day and the kidney function should be checked by measuring the serum creatinin. This monitoring is particularly important in older patients and at the same time treatment with heart glycosides (medicines to promote the function of the cardiac muscles) or diuretics (medicines to promote urine excretion). In the case of hypercalcemia (increased calcium concentration in the blood) or signs of reduced kidney function, the dose must be reduced or the treatment is interrupted. It is advisable to reduce the dose or to interrupt the treatment if the calcium content in the urine exceeds 7.5 mmol/24 hours (300 mg/24 hours).
Taking Dekristol 1000 I.E. Together with other medicines:
Inform your doctor or pharmacist if you take/use other medicines, have recently taken/applied other medicines or intend to accept/apply other medicines. The effects of DEKRISTOL 1000 I.E. can be impaired by simultaneous use of the following medicines:
Phenytoin (medicines for the treatment of epilepsy) or barbiturates (medicines for the treatment of epilepsy and sleep disorders)
Glucocorticoids (drugs for the treatment of certain allergic Diseases)
rifampicin and isoniazid (medicinal products for the treatment of tuberculosis)
Colestyramin (medicine for reducing a high cholesterol), laxative (laxative) with liquid paraffin
actinomycin (medicines for the treatment of cancer)
Imidazol (Medicines for the treatment of fungal diseases)
Orlistat (medicinal products for the treatment of overweight).
The effects/side effects of Dekristol 1000 I.E. can be reinforced by the simultaneous use of the following medicines:
Vitamin D metabolite or analoga (e.g. calcitriol): A combination with DEKRISTOL 1000 I.E. recommended. The calcium levels in the blood should be monitored.
Medicines for promoting urine excretion (thiazid diuretics): The reduction of calcium excretion via the kidney can lead to increased calcium concentrations in the blood (hypercalcaemia). The calcium levels in the blood and urine should therefore be increased by the simultaneous use of decristol 1000 I.E. Increase the calcium levels in the blood during treatment with vitamin D. In such cases, the treating doctor should carry out ECG monitoring as well as control of the calcium concentrations in the blood and in the urine and medication level in the blood.
Taking DEKRISTOL 1000 I.E. together with food and drinks:
DEKRISTOL 1000 I.E. should be taken either alone or together with food and drinks.
pregnancy and lactation:
If you are pregnant or breastfeed, or if you suspect that you are pregnant or intend to become pregnant, ask your doctor or pharmacist for advice before taking this drug.
pregnancy:
daily doses up to 500 i.e./Tag:
No risks in the specified dose area have so far been known. Long-lasting overdoses of vitamin D must be prevented during pregnancy, since the resulting hypercalcemia (increased calcium concentration in the blood) can lead to physical and mental disabilities as well as congenital heart and eye diseases of the child.
daily doses over 500 i.e./tag:
During pregnancy, decristol 1000 I.E. Overdoses of vitamin D during pregnancy must be prevented because long-lasting hypercalcemia (increased calcium concentration in the blood) can lead to physical and intellectual disabilities as well as innate heart and eye diseases of the child.
breastfeeding:
women are allowed to breastfeed 1000 I.E. during treatment. Vitamin D and its metabolic products pass into breast milk, which should be taken into account when administering additional vitamin D to infants.
Road and ability to use machines:
There is no evidence that Dekristol 1000 I.E. influences the ability to use machines.
Dekristol 1000 I.E. contains lactose and sucrose:
Please only take a decristol 1000 I.
3. How is Dekristol 1000 I.E. to be taken?
Always take this medicine exactly as described in this package insert or take the agreement with your doctor or pharmacist. Ask your doctor or pharmacist if you are not sure. The recommended dose is:
to prevent rachitis and osteomalacia in children and adults:
½ tablet decristol 1000 I.E. (corresponding to 0.0125 mg or 500 I.E. vitamin D3).
for prevention against rachitis in premature babies:
1 daily decristol 1000 I.E. (corresponding to 0.025 mg or 1000 i.e. vitamin D3). The dosage must be determined by the treating doctor.
To prevent vitamin D deficiency in children and adults with a recognizable risk:
Infants (0-12 months):
decristol 1000 i.e. is not suitable for infants up to one year. However, vitamin D3 tablets with lower strengths are available in stores.
Children, adolescents and adults:
daily ½ -1 tablet decristol 1000 I.E. (corresponding to 0.0125 - 0.025 mg or 500 - 1000 i.E. vitamin D3).
For supporting treatment of osteoporosis in adults:
1 daily decristol 1000 i.E. (corresponding to 0.025 mg or 1000 i.e. vitamin D3).
The tablet can be divided into the same doses. Take the tablets with enough water. Please ask your doctor about the necessary duration of the application.
daily doses over 500 i.e./tag:
During a long -term treatment with DEKRISTOL 1000 I.E. In daily doses over 500 i.E. the calcium levels in the blood and urine should be monitored regularly and the kidney function is checked by measuring the serum creatinin. If necessary, a dose adjustment must be made according to the blood calcium values.
Use for infants and toddlers:
let the tablet disassemble on a teaspoon with water or milk and add the dissolved tablet to the child directly, preferably during a meal. The addition of the tablets to a bottle or pilot period for infants is not recommended, since no complete vitamin D intake can be guaranteed. If the tablets are still to be administered in the food, the addition is only brought to the boil after the food. When using vitaminized food, the amount of vitamin D contained therein must be taken into account. Infants receive 1000 I.E. from the second week of life until the end of the first year of life. In the second year of life, further gifts of Dekristol 1000 I.E. are recommended, especially during the winter months.
If you have taken a larger amount of Dekristol 1000 I.E. than you should:
If you or your child have taken a larger amount of decristol 1000 I. The signs of an overdose are not very characteristic and express themselves in nausea, vomiting, initially often diarrhea, later constipation, loss of appetite, mattness, head, muscle, muscle and joint pain, arrhythmias (irregular heartbeat), azotemia (increased nitrogen concentration in the blood), increased thirst , increased urge to urinate and in the final phase drying out. Please ask your doctor about the signs of an overdose of vitamin D. There is no special antidote. Your doctor will initiate the necessary countermeasures.
If you have forgotten the intake of Dekristol 1000 I.E.:
don't take twice the amount if you have forgotten the prior intake.
If you cancel the intake of Dekristol 1000 I.E.:
When an interruption or early end of the treatment, your symptoms can deteriorate or reappear. Please ask your doctor.
If you have any further questions about taking this medicine, please contact your doctor or pharmacist.
4. What side effects are possible?
Like all medicines, this medicine can also have side effects, but this does not have to occur with everyone. The frequencies of the side effects are not known because no larger clinical studies have been carried out that allow the frequencies to estimate.
break the intake of Dekristol 1000 I.E. and immediately inform your doctor if one of the following signs of a severe allergic reaction occurs:
swollen face, swelling of the lips, the tongue or throat
swallowing disorders < Br> Nessel rash and breathing difficulties. The following side effects can occur:
increased calcium concentration in the blood (hypercalcemia) and increased calcium concentration in urine (hypercalciuria)
symptoms in the gastrointestinal tract such as constipation, bloating, nausea, abdominal pain or diarrhea
over sensitivity reactions Like itching, rash or hives.
Announcement of side effects:
If you notice side effects, contact your doctor or pharmacist. This also applies to side effects that are not specified in this package insert. You can also directly see the Federal Institute for Medicines and Medical Devices, Pharmacovigilance, Kurt-Georg-Kiesinger Allee 3, D-53175 Bonn, website: www.bfarm.de. By reporting side effects, you can help to provide more information about the safety of this drug.
5. How is Dekristol 1000 I.E. to be kept?
keep this medicine for children inaccessible. You may no longer use this drug according to the "or" usable expiry date on the blister and the converter after "Verw. Bis:" or "usable. The expiry date refers to the last day of the specified month. Do not store over 25 ° C. Keep the blister in the box to protect the content from light. Do not dispose drugs in the wastewater or household waste. Ask your pharmacist how to dispose of the medicine if you no longer use it. You help to protect our environment.
6. Content of the package and further information
What Dekristol 1000 I.E. One tablet contains 10 mg Colecalciferol dry concentrate (corresponding to 25 micrograms Colecalciferol = 1000 I.E. Vitamin D3). The other ingredients are: lactose monohydrate, microcrystalline cellulose, cornstarch, modified cornstarch, carboxymethylar sterice sodium (type A) (ph.eur.), Sucrose (sugar), high-disperses silicon dioxide, magnesium stearate (ph.), Sodium ascor Triglycerides, all-rac alpha-tocopherol.
How Dekristol 1000 I.E. Tablets looks and contents of the pack:
DEKRISTOL 1000 I.E. is an elongated, bikonvexe, white to yellowish tablet with a break. DEKRISTOL 1000 I.E. is available in packs with 20, 30, 50, 100 and 200 tablets. Not all package sizes may be placed on the market.
Pharmaceutical entrepreneur and manufacturer:
MiBe GmbH Arzneimittel
Munich Straße 15
06796 Brehna
Tel.: 034954/247-0
Fax: 034954/247-100
Using information was last revised in February 2017.
Source: Information from the package insert
as of: 10/2017
Made by: Mibe GmbH Arzneimatic
Areas of application
- prevention against rachitis - prevention against bone softification (osteomalacia )-Prevention of a vitamin D deficiency-osteoporosis (bone loss)
Colecalciferol dry concentrate, Colecalciferol, Colecalciferol, lactose-1 water, lactose, cellulose, microcrystalline, corn thickness, strength [OCT -1-en-1-yl) BUTANDIOAT] -Natrium salt, carboxymethylar, sodium type A, saccharosis, silicon dioxide, high-disperse, magnesium stair (vegetable), sodium ascorbat, triglyceride, medium-chain,
-α-tocopherol
dosage
Tablets
Application notes
The total dose should not be exceeded without consulting a doctor or pharmacist.
Type of application?
Older children and adults: take the medicine with liquid (e.g. 1 glass of water). Infants and toddlers: let the medicine decay on a teaspoon in a small amount of water or milk. The dissolved tablet can be given to the child directly in the mouth.
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. In order to prevent rachitis, infants receive the medicine from the second week of life until the first year of life. From the age of 2, further gifts, especially in the winter months, are recommended.
overdosing?
In the case of an overdose, there may be increased calcium values in the blood with cardiac arrhythmias, thirst, lack of fluid, weakness or weakness, consciousness disorders as well as calcium deposits in vessels and tissue. 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.
mode of action
How does the ingredient of the drug work?
The active ingredient intervenes in protein production. It triggers the formation of a protein that binds calcium itself and releases the bloodstream. In this way, the blood calcium level is increased, this calcium is then available for bone structure.
Contraindications
What speaks against an application?
Always:
- hypersensitivity to the ingredients
- Increased calcium values
- increased calcium excretion in urine
- increased vitamin D levels in the blood
- kidney stones
You with your doctor or pharmacist:
- tendency to form kidney stones
- disrupted calcium excretion
- disrupted phosphate excretion
- limited mobility
- sarcoidosis (Boeck disease) (rare, frequently inherited Disease, with the formation of small tissue, especially in the lung)
metabolic disorder (pseudohypoparathyroidism)
Which age group must be observed?
- Children and adolescents under the age of 18: In this age group, the drug should only be used in certain areas of application. Please ask your doctor or pharmacist, if you have questions regarding this topic.
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?
For the medicine, only side effects are currently described that have so far only occurred in exceptional cases.
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?
- Beware of allergy to ascorbic acid (vitamin C)!
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.
caution in the event of intolerance to sucrose. If you have to adhere to a diabetes diet, you should take the sugar content into account.
- There can be medicines that occur with which interactions occur. Therefore, you should generally provide the doctor or pharmacist before treatment with a new medicine. This also applies to medicines that you buy yourself, only apply occasionally or that the application has been available for some time.
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MIBE Arzneimittel Decristol 1,000 i.E. tablets

AED 53.00
+ AED 44.00 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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