Vitamin A plays an essential role in the process of vision (ensuring proper functioning of the retina), is necessary for growth, regeneration, differentiation, and function of epithelial tissue, skin, and mucous membranes. It participates in bone calcification and structure formation, in the reproductive process, and in embryonic development of the fetus.
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Vitamin E is a substance obtained from natural plant oils, necessary for the proper functioning of the body. It exhibits biological activity 50% stronger than commonly used synthetic vitamin.
Epidemiological studies indicate a correlation between daily intake of vitamin E and the risk of coronary heart disease, carotid atherosclerosis, and other diseases whose etiology is associated with oxidative stress.
The medicine TOKOVIT A + E is intended for the prevention and supplementation of vitamins A and E:
Do not take TOKOVIT A + E if:
Before taking the medicine, consult a doctor.
Pregnant women can take TOKOVIT A + E only after consulting a doctor and in the doses prescribed by them, as taking increased amounts of vitamin A can be hazardous to the fetus.
Taking high doses of vitamin E during pregnancy is not recommended due to the lack of data on the safety of its use.
Before taking the medicine, consult a doctor.
Vitamin A passes into breast milk, which can lead to its overdose in the child. Breastfeeding women can take TOKOVIT A + E only after consulting a doctor and in the doses prescribed by them, as taking increased amounts of vitamin A can be hazardous to the child.
Taking high doses of vitamin E during breastfeeding is not recommended due to the lack of data on the safety of its use.
Taking TOKOVIT A + E does not affect the ability to drive vehicles and operate machinery.
The medicine contains peanut oil (from peanuts). If you are allergic to peanuts or soy, do not take this medicine.
Tell your doctor about all the medicines you have taken recently, even those that are available
without a prescription.
Neomycin, cholestyramine (colestipol), and liquid paraffin reduce the absorption of vitamin A. Concurrent use of products containing vitamin A (carotenes), synthetic analogs of vitamin A (acitretin, etretinate, tretinoin), and bexarotene may lead to the occurrence of hypervitaminosis A symptoms. Vitamin A, when administered in doses several times higher than recommended, enhances the effect of anticoagulant medicines (warfarin derivatives). Oral contraceptives may increase the concentration of vitamin A in the blood.
Vitamin E may act antagonistically to vitamin K, especially in people treated with oral anticoagulants or estrogens. The use of other agents with antioxidant activity (vitamin C, selenium, ubiquinone, sulfur-containing amino acids) may alleviate some symptoms of vitamin E deficiency. Concurrent use of iron preparations weakens the effect of vitamin E, so it is recommended to maintain a few-hour interval between taking these medicines. Vitamin E may reduce the need for insulin and digitalis glycosides.
The medicine is intended for oral use.
For prophylaxis, unless otherwise prescribed by a doctor, usually 1 or 2 capsules are taken during the first meal, for adolescents and adults.
Therapeutically: according to the doctor's instructions, depending on the degree of deficiency.
If you feel that the effect of TOKOVIT A + E is too strong or too weak, consult a doctor.
In case of taking a significantly higher dose of the medicine than recommended, consult a doctor or
pharmacist.
Symptoms of acute vitamin A poisoning may occur in children after taking 75,000 to 350,000 IU, and in adults after taking a dose of 1,000,000 IU. Characteristic symptoms of vitamin A overdose are headaches, nausea, vomiting, auditory hallucinations, vision disturbances, swelling of subcutaneous tissue and tissues around long bones, muscle-bone-joint pain, skin and mucous membrane symptoms. Additionally, hypercalcemia, petechiae, bleeding, nervousness, fatigue, irritability, and drowsiness have been observed. Very significant and prolonged overdose of vitamin A may be accompanied by other adverse symptoms related to the cardiovascular system, central nervous system, gingivitis, liver damage symptoms, respiratory function disorders, dermatological changes, and skin discoloration, osteoporosis, bone hardening, and other changes considered less specific.
High doses of vitamin E (400 to 800 IU per day) taken for a longer period may cause diarrhea, abdominal pain, and other gastrointestinal disorders, as well as fatigue, weakness, blurred vision, headaches, rash, disorders of sexual gland function, and decreased levels of thyroid hormones in the blood.
In case of overdose symptoms, it is necessary to stop taking the product and consult a doctor.
Do not take a double dose to make up for the missed dose.
Like any medicine, TOKOVIT A + E can cause side effects.
Vitamins A and E are generally well-tolerated, and their intake in recommended doses is not associated with a significant risk of side effects. Symptoms of side effects are related to the overdose of the product (see section 3).
In some people, other side effects may occur during the use of the medicine. If other side effects occur that are not listed in this leaflet, inform your doctor about them.
Keep the medicine out of sight and reach of children.
Do not use TOKOVIT A + E after the expiration date stated on the packaging.
Store in the original packaging, at a temperature below 25°C.
To obtain more detailed information, contact the representative of the responsible entity:
“HASCO-LEK” Pharmaceutical Production Company S.A.
51-131 Wrocław, ul. Żmigrodzka 242 E
tel. (071) 352 95 22
fax (071) 352 76 36
Drug Information Department
tel. (22) 742 00 22
email: informacjaoleku@hasco-lek.pl
Date of leaflet preparation:
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