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Complivit® Antistress (Tablets) Instructions for Use

Marketing Authorization Holder

Pharmstandard-UfaVITA OJSC (Russia)

Dosage Form

Bottle OTC Icon Complivit® Antistress Tablets

Dosage Form, Packaging, and Product Composition

Composition: retinol acetate (vitamin A), alpha tocopherol acetate (E), thiamine hydrochloride (B1), riboflavin (B2), pyridoxine hydrochloride (B6), ascorbic acid, nicotinamide, folic acid, calcium pantothenate, cyanocobalamin (B12), dry extract of ginkgo biloba leaves, dry extract of motherwort herb, magnesium oxide, zinc oxide, sodium selenite, copper sulfate, potato starch, citric acid (E330), kollidon (E1201), lactose, magnesium stearate, talc (E553), polyvinylpyrrolidone (E1201), hydroxypropyl methylcellulose (E464), titanium dioxide (E171), polyethylene glycol (E1521), yellow dye “Sunset Yellow” (E110).

Content of biologically active components per 1 tablet: vitamin A – 1 mg±25%, E – 15 mg ±20%, PP – 20 mg±25%, B1 – 2 mg±20%, B2 – 2 mg±20%, B6 – 2 mg±20%, C -50 mg±20%, folic acid – 0.4 mg±35%, B12 – 3 mcg±35%, zinc – 12 mg ±20%, copper – 1 mg ±20%, magnesium – 10 mg±20%, selenium – 25 mcg±35%, flavonol glycosides – 8-15 mg, calcium pantothenate – 5 mg±20%.

Release form and packaging
Tablets 525 mg.

Therapeutic Category

Dietary supplement – source of flavonoids, vitamins and trace elements

Scope of Application

Of the Complivit® Antistress product

Recommended as a dietary supplement – an additional source of vitamins A, C, E, B group (B1, B2, B6, B12, folic acid, calcium pantothenate, nicotinamide), mineral elements (copper, selenium, zinc, magnesium), and a source of flavonoglycosides.

Indications

  • Use as a dietary supplement to provide additional intake of vitamins A, C, E, and B-group vitamins (B1, B2, B6, B12, folic acid, calcium pantothenate, nicotinamide).
  • Use as a source of essential mineral elements, including copper, selenium, zinc, and magnesium.
  • Use as a source of flavonol glycosides for general nutritional support in conditions associated with increased requirements for these micronutrients.

ICD codes

ICD-10 code Indication
E63.9 Nutritional deficiency, unspecified
ICD-11 code Indication
5B7Z Malnutrition, unspecified
8D40.0 Encephalopathy due to nutritional deficiency
8D40.1 Neuropathy due to nutritional deficiency
8D40.2 Myopathy due to nutritional deficiency
8D40.3 Intellectual developmental disorder due to nutritional deficiency
8D40.Y Other specified diseases of the nervous system due to nutritional deficiency

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 once daily with a meal. Swallow the tablet whole with a sufficient amount of water; do not chew or crush.

The recommended duration of continuous use is one month. Adhere strictly to the specified dosage; do not exceed it. If a dose is missed, take it as soon as remembered, but do not double the dose to compensate for a missed one.

Adverse Reactions

Adverse reactions are possible and may include allergic reactions such as skin rash, itching, urticaria, and redness of the skin.

Gastrointestinal disturbances, including nausea, epigastric discomfort, or diarrhea, may occur. Discontinue use immediately and consult a physician if any adverse reactions manifest.

Drug Interactions with Other Medicinal Products and Substances

Do not take concurrently with other vitamin-mineral complexes to prevent the risk of overdose. The interval between taking this product and tetracycline antibiotics or fluoroquinolones should be at least 2 hours due to potential impaired absorption of these antimicrobials.

Consult a physician before use if you are taking any other prescription or over-the-counter medications, including anticoagulants, antacids, or thyroid medications.

Contraindications for Use and Patient Groups at Risk

  • Hypersensitivity or individual intolerance to any of the components of the product, including active substances and excipients such as lactose.
  • Pregnancy at any trimester is an absolute contraindication for use.
  • Breastfeeding (lactation period) is a contraindication for use.
  • Use in children and adolescents under 18 years of age is not recommended due to lack of data.

Overdose Symptoms and Recommended Management Procedures

Symptoms of acute overdose may include severe headache, nausea, vomiting, diarrhea, and generalized weakness. Chronic overdose can lead to symptoms of hypervitaminosis, particularly for fat-soluble vitamins A and E.

In case of suspected overdose, immediately discontinue use of the product. Initiate symptomatic and supportive treatment. Gastric lavage and administration of activated charcoal may be considered. Seek immediate medical attention for evaluation and management.

Dispensing Status

Available to the public through pharmacy chains and specialized stores, departments of the retail network.

Storage Conditions

Store in a dry place, protected from light, at a temperature not exceeding 25°C (77°F).

Shelf Life

Shelf life – 2 years.

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

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