all-rac-Phytonadione
Vitacon contains phytonadione (vitamin K - fat-soluble), which participates in the formation of certain blood clotting factors. Vitacon is used:
Before starting treatment with Vitacon, discuss it with your doctor or pharmacist.
Tell your doctor or pharmacist about all the medicines you are taking, or have recently taken, and about the medicines you plan to take. The use of phytonadione may cause temporary resistance to the action of oral anticoagulant drugs (coumarin and indandione derivatives).
If you are pregnant or breastfeeding, think you may be pregnant or plan to have a child, consult your doctor or pharmacist before taking this medicine. The medicine may be used during pregnancy only in cases where the benefit to the mother outweighs the potential risk to the fetus. Caution should be exercised when using the medicine in breastfeeding women.
The medicine does not affect the ability to drive and use machines.
If you have been diagnosed with intolerance to some sugars, you should consult your doctor before taking the medicine. The medicine may cause allergic reactions due to the presence of quinoline yellow. The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means that the medicine is considered "sodium-free".
This medicine should always be taken according to the doctor's recommendations. If you are unsure, consult your doctor or pharmacist. Coagulation disorders in adults caused by oral anticoagulant drugs (coumarin and indandione derivatives) The initial dose is usually 10 mg (maximum 30 mg or exceptionally 50 mg). The frequency and size of subsequent doses will be determined by the doctor based on prothrombin time measurements and the patient's clinical condition. If after 12-48 hours after administration of the medicine the prothrombin time has not improved satisfactorily, the dose can be repeated. Coagulation disorders in adults caused by other factors The initial dose is 10 to 30 mg, exceptionally 50 mg. The dose size depends on the patient's condition and response to treatment. The basic procedure should involve, if possible, correcting the dose of drugs that disrupt coagulation mechanisms (antibiotics, salicylates, sulfonamides). Phytonadione should be used when coagulation disorders are severe enough that changing the dose of the taken medicine does not ensure their rapid resolution, or when changing the dose is not possible. Note: Oral administration of vitamin K is justified only when it can be absorbed from the gastrointestinal tract. If the amount of bile secreted into the gastrointestinal tract is insufficient, the doctor will recommend additional oral administration of bile salts.
No symptoms of phytonadione overdose are known.
Do not take a double dose to make up for a missed dose.
Like all medicines, this medicine can cause side effects, although not everybody gets them. After taking phytonadione in the form of oral tablets, no side effects have been observed.
If you experience any side effects, including those not listed in this leaflet, please inform your doctor or pharmacist. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products Al. Jerozolimskie 181C 02-222 Warsaw Tel.: +48 22 49 21 301 Fax: +48 22 49 21 309 Website: https://smz.ezdrowie.gov.pl Side effects can also be reported to the marketing authorization holder. By reporting side effects, you can help provide more information on the safety of this medicine.
Store in a temperature below 25°C. Store in the original package to protect from moisture. The medicine should be stored out of sight and reach of children. Do not use this medicine after the expiry date stated on the carton and blister. The expiry date refers to the last day of the month stated. The inscription on the packaging after the abbreviation EXP means the expiry date, and after the abbreviation Lot/LOT means the batch number. Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Vitacon is a yellow, round, biconvex effervescent tablet. Vitacon is available in blisters of aluminum/PVC in a cardboard box. The package contains 30 tablets.
Zakłady Farmaceutyczne POLPHARMA S.A. ul. Pelplińska 19, 83-200 Starogard Gdański tel. +48 22 364 61 01
Zakłady Farmaceutyczne POLPHARMA S.A. Production Plant in Nowa Dęba ul. Metalowca 2, 39-460 Nowa Dęba Date of last revision of the leaflet:December 2024
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