Vectrum® Calcium (Tablets) Instructions for Use
Marketing Authorization Holder
Akrikhin Chemical and Pharmaceutical Plant, JSC (Russia)
ATC Code
A12AX (Calcium preparations in combination with vitamin D and/or other drugs)
Dosage Form
| Vectrum® Calcium | Chewable tablets: 30 pcs. |
Dosage Form, Packaging, and Composition
Chewable tablets are flat-cylindrical, with a bevel, from white to white with a yellowish or creamy tint with the presence of gray inclusions, with a characteristic fruity odor.
| 1 tab. | |
| Colecalciferol (vit. D3) | 200 IU |
| Phytomenadione (vit. K1) | 200 mcg |
| Ascorbic acid (vit. C) | 60 mg |
| Pyridoxine hydrochloride (vit. B6) | 2.4 mg |
| Calcium (as calcium carbonate) | 200 mg |
Excipients: lactose, sorbitol, aspartame, powdered flavoring with fruity odor, magnesium stearate, anhydrous citric acid.
10 pcs. – blister packs (3) – cardboard packs.
Clinical-Pharmacological Group
Drug regulating calcium and phosphorus metabolism
Pharmacotherapeutic Group
Multivitamin agent + multimineral
Pharmacological Action
Combined multivitamin preparation that regulates the metabolism of calcium and phosphorus in the body. It replenishes the deficiency of calcium and vitamin D3 in the body.
Calcium is involved in the formation of bone tissue, mineralization of teeth, blood clotting, regulation of nerve conduction and muscle contractions, and in maintaining stable cardiac activity.
Colecalciferol (vitamin D3) regulates the metabolism of calcium and phosphorus in the body and promotes the complete absorption of calcium.
Pharmacokinetics
Data on the pharmacokinetics of Vectrum Calcium are not provided.
Indications
Treatment and prevention of conditions accompanied by a deficiency of calcium and vitamin D3 in the body
- Prevention and complex therapy of osteoporosis and its complications (bone fractures);
- Replenishment of calcium and vitamin D3 deficiency in the elderly.
ICD codes
| ICD-10 code | Indication |
| E55 | Vitamin D deficiency |
| E58 | Dietary calcium deficiency |
| M80 | Osteoporosis with pathological fracture |
| M81 | Osteoporosis without pathological fracture |
| M81.0 | Postmenopausal osteoporosis |
| M81.1 | Postoophorectomy osteoporosis |
| M81.2 | Osteoporosis due to immobilization |
| M81.4 | Drug-induced osteoporosis |
| M81.8 | Other osteoporosis (senile osteoporosis) |
| ICD-11 code | Indication |
| 5B57.Z | Vitamin D deficiency, unspecified |
| 5B5K.1Z | Calcium deficiency, unspecified |
| 8D40.2 | Myopathy due to nutritional deficiency |
| FB83.11 | Postmenopausal osteoporosis |
| FB83.12 | Osteoporosis due to disuse |
| FB83.13 | Drug-induced osteoporosis |
| FB83.14 | Osteoporosis due to malabsorption |
| FB83.1Z | Osteoporosis, unspecified |
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. |
For prophylactic use in adults, administer 1 tablet once daily.
Chew the tablet thoroughly before swallowing.
For the treatment of osteoporosis, the dosing regimen and duration of therapy are set individually by a physician.
Adjust the dose or temporarily discontinue use if serum calcium or creatinine levels increase.
Consider dietary intake and other sources of vitamin D3 to avoid overdose.
Do not use concurrently with other vitamin-mineral complexes containing Calcium and vitamin D3.
Be aware that acidic foods may increase, and weakly alkaline foods may decrease, calcium absorption.
With long-term use, monitor calcium levels in urine and calcium and creatinine in blood serum.
Adverse Reactions
From the digestive system: constipation, diarrhea, flatulence, nausea, abdominal pain.
From the metabolism: with long-term use – hypercalcemia, hypercalciuria.
Other: allergic reactions.
Contraindications
- Hypercalcemia;
- Hypercalciuria;
- Nephrolithiasis (formation of calcium stones);
- Renal failure;
- Osteoporosis due to prolonged immobilization;
- Phenylketonuria;
- Hypervitaminosis D3;
- Children and adolescents under 18 years of age;
- Hypersensitivity to the drug components.
Use in Pregnancy and Lactation
Adequate and strictly controlled studies on the safety of Vectrum Calcium use during pregnancy and lactation have not been conducted.
Use in Renal Impairment
Contraindicated in renal failure.
Pediatric Use
The drug is contraindicated in children and adolescents under 18 years of age.
Special Precautions
If the concentration of calcium and creatinine in the blood serum increases, the dose should be reduced or the drug should be temporarily discontinued.
To avoid overdose, additional intake of vitamin D3 from other sources should be taken into account. It is not recommended to use simultaneously with vitamin-mineral complexes containing Calcium and vitamin D3.
When taking the drug, it should be taken into account that the acidic reaction of food products increases, and the weakly alkaline reaction decreases the absorption of calcium.
Control of laboratory parameters
With long-term use of Vectrum Calcium, control of calcium content in urine, calcium and creatinine in blood serum is necessary.
Overdose
Symptoms: nausea, vomiting, polyuria, constipation, pain in the epigastric region, hypercalcemia, hypercalciuria.
Treatment: gastric lavage; if necessary, symptomatic therapy is carried out.
Drug Interactions
The activity of vitamin D3 may decrease when used simultaneously with phenytoin and barbiturates.
Simultaneous use of Vectrum Calcium and cardiac glycosides enhances the effect of the latter (monitoring of ECG and clinical condition of the patient is necessary).
When prescribing Vectrum Calcium and antibiotics from the tetracycline group simultaneously, the interval between taking the drugs should be at least 3 hours, because Calcium and vitamin D3 increase the absorption of tetracyclines from the gastrointestinal tract.
Corticosteroids reduce the absorption of calcium.
Concomitant use of Vectrum Calcium and thiazide-like diuretics increases the risk of hypercalcemia by enhancing the reabsorption of calcium from the lumen of the renal tubules. Furosemide and other “loop” diuretics, on the contrary, increase the excretion of calcium by the kidneys.
Storage Conditions
The drug should be stored in a dry, light-protected place at a temperature not exceeding 25°C (77°F).
Shelf Life
Shelf life – 2 years.
Pharmacy supply conditions
The drug is approved for use as an over-the-counter product.
Dispensing Status
Over-the-Counter
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