Megadin (Tablets) Instructions for Use
Marketing Authorization Holder
Mecom Saglik Urunleri, San. ve Tic. A.S. (Turkey)
Manufactured By
Abdi Ibrahim Ilac Sanayi ve Tic., A.S. (Turkey)
ATC Code
A11AA03 (Multivitamins and other minerals, including their combinations)
Dosage Form
| Megadin | Coated tablets: 30 pcs. |
Dosage Form, Packaging, and Composition
Coated tablets brown in color, round, biconvex.
| 1 tab. | |
| Retinol | 10 thousand IU |
| Colecalciferol | 500 IU |
| Tocopherol | 10 mg |
| Thiamine | 20 mg |
| Riboflavin | 5 mg |
| Pyridoxine | 10 mg |
| Ascorbic acid | 150 mg |
| Cyanocobalamin | 5 mcg |
| Biotin | 250 mcg |
| Nicotinamide | 50 mg |
| Pantothenic acid | 11.6 mg |
| Calcium | 50 mg |
| Phosphate | 25.8 mg |
| Magnesium | 36.2 mg |
| Iron | 10 mg |
| Copper | 1 mg |
| Zinc | 500 mcg |
| Manganese | 500 mcg |
| Molybdenum | 100 mcg |
Excipients: croscarmellose sodium (acdisol), D-mannitol, talc, polyvinylpyrrolidone K-30, microcrystalline cellulose PH 102, magnesium stearate, lactose, isopropyl alcohol.
Coating composition Opadry YS-1-7006 clear, ariavit brown, opalux brown, water.
10 pcs. – blisters (3) – cardboard packs.
Clinical-Pharmacological Group
Multivitamins with macro- and microelements
Pharmacotherapeutic Group
Multivitamin agent + multimineral
Pharmacological Action
Megadin is a combination of vitamins and minerals.
Vitamin A (Retinol): is a fat-soluble vitamin. Vitamin A deficiency leads to keratomalacia, xerophthalmia, and night blindness.
Vitamin E, due to its antioxidant action, protects cells from damage by free radicals.
Vitamin C is involved in tissue regeneration and collagen formation.
The B complex of vitamins is involved in the conversion of carbohydrates, protein, and fats.
Vitamin D ensures normal development of bones and teeth and regulates calcium utilization in the body.
Nicotinamide and Biotin are involved in various biochemical reactions.
Phosphate and Calcium are necessary for bone mineralization.
Iron and Copper are involved in the process of hematopoiesis, Zinc, Molybdenum, Magnesium, and Manganese are essential elements.
Indications
- Treatment of vitamin and mineral deficiency during convalescence after prolonged illnesses, in the pre- and postoperative period;
- In cases of malabsorption due to gastrointestinal diseases.
ICD codes
| ICD-10 code | Indication |
| E50-E64 | Other types of nutritional deficiencies (E50-E64) |
| Z54 | Convalescence |
| Z73.0 | Burn-out |
| Z73.3 | Stress, not elsewhere classified (physical and mental strain) |
| ICD-11 code | Indication |
| 5B7Z | Malnutrition, unspecified |
| QB7Z | Convalescence, unspecified |
| QD85 | Burn-out |
| QE01 | Stress, not elsewhere classified |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Take one tablet orally once daily.
Administer the tablet during breakfast to enhance absorption and minimize potential gastrointestinal discomfort.
Swallow the tablet whole with a full glass of water; do not crush or chew.
The duration of treatment is determined by the physician based on the patient’s clinical condition and nutritional status.
Do not exceed the recommended daily dose.
Concurrent use with other vitamin or mineral supplements is not recommended without medical supervision due to the risk of hypervitaminosis or exceeding safe intake levels for certain minerals.
In patients with malabsorption syndromes, the therapeutic response should be monitored clinically.
Discontinue use and consult a physician if signs of hypersensitivity or other adverse reactions occur.
Adverse Reactions
Allergic reactions are possible. In high doses and with prolonged use, reactions such as allergic rash and ulceration of mucous membranes are possible.
Contraindications
- Hypervitaminosis A or D;
- Hypercalcemia or hypercalciuria;
- Pregnancy;
- Hypersensitivity to the components of the drug.
Use in Pregnancy and Lactation
Contraindicated during pregnancy.
Special Precautions
Megadin should be used in the recommended doses. In high doses, Megadin can cause hypervitaminosis.
Megadin should not be used simultaneously with other medicines containing vitamins and minerals without a doctor’s prescription.
Overdose
It must be emphasized that Megadin, in the doses recommended in the leaflet, does not cause symptoms of overdose or poisoning. Since Megadin contains fat-soluble vitamins A and D, signs of acute or chronic overdose may develop after a single high dose or with prolonged use.
Symptoms signs of vitamin A overdose include headache, dizziness, irritability, confusion, loss of appetite, vomiting, diarrhea, dry skin, and visual disturbances. The main signs of vitamin D overdose are nausea, vomiting, constipation, headache, dizziness, drowsiness, and deposition of calcium in internal organs (kidneys).
Treatment: in case of overdose, it is recommended to discontinue this medicine and carry out symptomatic treatment.
Drug Interactions
Do not use simultaneously with tetracyclines due to possible undesirable interaction.
If tetracyclines are indicated during the use of Megadin, the interval between taking these two medicines should be approximately 2 hours.
Storage Conditions
Store the drug at a temperature not exceeding 25°C (77°F), in a dry place. Keep out of reach of children.
Shelf Life
Shelf life – 2 years. Do not use after the date indicated on the packaging.
Dispensing Status
The drug is approved for use as an over-the-counter product.
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical Disclaimer