Deltius 25000 iu витамин д инструкция

SUMMARY OF PRODUCT CHARACTERISTICS

1 NAME OF THE MEDICINAL PRODUCT

DELTIUS 25 000 I.U. /2.5 ml oral solution

2. QUALITATIVE AND QUANTITATIVE COMPOSITION

A single-dose bottle of 2.5 ml oral solution contains: 25 000 I.U. cholecalciferol (vitamin D₃), equivalent to 0.625 mg.

1 ml oral solution contains 10 000 I.U. cholecalciferol (vitamin D₃), equivalent to 0.25 mg

For the full list of excipients, see section 6.1.

3. PHARMACEUTICAL FORM

Oral Solution in single dose container

Clear and colourless to greenish-yellow oily solution without visible solid particles and/or precipitate

4. CLINICAL PARTICULARS

4.1 Therapeutic indications

■    Prophylaxis of rickets and osteomalacia in children and adults

■    Prophylaxis of rickets in preterm newborns

■    Prophylaxis of vitamin D deficiency in children and adults with an identified risk

■    Prophylaxis of vitamin D deficiency in children and adults with malabsorption

■    Treatment of rickets and osteomalacia in children and adults

4.2 Posology and method of administration

Posology

■ Paediatric posology

—    prevention of deficiency 0-1 years 25000 IU (1 bottle) every 8 weeks

—    prevention of deficiency 1-18 years 25000 IU (1 bottle) every 6 weeks

—    treatment of deficiency 0-18 years 25000 IU (1 bottle) once every 2 weeks for 6 weeks (followed by maintenance therapy of 400-1000 IU/day)

■    Pregnancy and breastfeeding

— The high strength formulation is not recommended

■    Adult

—    prevention of vitamin D₃ deficiency 25000 IU/month (1 bottle), higher doses may be required in certain situations, see below

—    as an adjunct to specific therapy for osteoporosis: 25000 IU/month (1 bottle)

—    treatment of vitamin D₃ deficiency (<25 ng/ml) 50000 IU/week (2 bottles) for 6-8 weeks, followed by maintenance therapy (1400-2000 IU/day may be required; follow-up 25(OH)D measurements should be made approximately three to four months after initiating maintenance therapy to confirm that the target level has been achieved)

Certain populations are at high risk of vitamin D₃ deficiency, and may require higher doses and monitoring of serum 25(OH)D:

—    Institutionalised or hospitalised individuals

—    Dark skinned individuals

—    Individuals with limited effective sun exposure due to protective clothing or consistent use of sun screens

—    Obese individuals

—    Patients being evaluated for osteoporosis

—    Use of certain concomitant medications (eg, anticonvulsant medications, glucocorticoids)

—    Patients with malabsorption, including inflammatory bowel disease and coeliac disease

—    Those recently treated for vitamin D3 deficiency, and requiring maintenance therapy.

Method of administration

Patients should be advised to take DELTIUS preferably with meal (see section

5.2 Pharmacokinetic properties — “Absorption”).

The product should be shaken before use.

DELTIUS has a taste of olive oil. DELTIUS can be taken as is from the bottle or to facilitate intake it can also mixed with a small amount of cold or lukewarm food immediately prior to use. The patient should be sure to take the entire dose.

In children, DELTIUS can be mixed with a small amount of children’s foods, yogurt, milk, cheese or other dairy products. The parents should be warned not to mix DELTIUS into a bottle of milk or container of soft foods in case the child does not consume the whole portion, and does not receive the full dose. The parents should ensure that their child takes the entire dose. For children who are not breast-feeding the prescribed dose should be administered with a meal.

See also section 6.6 Special precautions for handling and disposal.

4.3    Contraindications

Hypersensitivity to the active ingredient, cholecalciferol (vitamin D₃), or to any of the excipients listed in section 6.1.

Hypercalcaemia, hypercalciuria Hypervitaminosis D

Kidney stones (nephrolithiasis, nephrocalcinosis) in patients with current chronic hypercalcaemia

4.4    Special warnings and precautions for use

Vitamin D3 should be used with caution in patients with impairment of renal function and the effect on calcium and phosphate levels should be monitored. The risk of soft tissue calcification should be taken into account.

Caution is required in patients receiving treatment for cardiovascular disease (see section 4.5 Interaction with other medicinal products and other forms of interaction — cardiac glycosides including digitalis).

DELTIUS should be prescribed with caution in patients with sarcoidosis, due to a possible increase in the metabolism of vitamin D₃ in its active form. In these patients the serum and urinary calcium levels should be monitored.

Allowances should be made for the total dose of vitamin D3 in cases associated with treatments already containing vitamin D, foods enriched with vitamin D3, cases using milk enriched with vitamin D, and the patient’s level of sun exposure.

There is no clear evidence for causation between vitamin D3 supplementation and renal stones, but the risk is plausible, especially in the context of concomitant calcium supplementation. The need for additional calcium supplementation should be considered for individual patients. Calcium supplements should be given under close medical supervision.

Oral administration of high-dose vitamin D₃ (500,000 IU by single annual bolus) was reported to result in an increased risk of fractures in elderly subjects, with the greatest increase occurring during the first 3 months after dosing.

During long-term treatment with a daily dose exceeding 1,000 IU vitamin D₃ the serum calcium values must be monitored.

4.5    Interactions with other medicinal products and other forms of interaction

Concomitant use of anticonvulsants (such as phenytoin) or barbiturates (and possibly other drugs that induce hepatic enzymes) may reduce the effect of vitamin D₃ by metabolic inactivation.

In cases of treatment with thiazide diuretics, which decrease urinary elimination of calcium, monitoring of serum calcium concentration is recommended.

Concomitant use of glucocorticoids can decrease the effect of vitamin D₃.

In cases of treatment with drugs containing digitalis and other cardiac glycosides, the administration of vitamin D3 may increases the risk of digitalis toxicity (arrhythmia). Strict medical supervision is needed, together with serum calcium concentration and electrocardiographic monitoring if necessary.

Simultaneous treatment with ion exchange resin such as cholestyramine, colestipol hydrochloride, orlistat or laxative such as paraffin oil may reduce the gastrointestinal absorption of vitamin D₃.

The cytotoxic agent actinomycin and imidazole antifungal agents interfere with vitamin D₃ activity by inhibiting the conversion of 25-hydroxyvitamin D₃ to 1,25-dihydroxyvitamin D₃ by the kidney enzyme, 25-hydroxyvitamin D-1-hydroxylase.

4.6 Fertility, pregnancy and lactation

In pregnancy and lactation the high strength formulation is not recommended and a low strength formulation should be used.

Pregnancy

There are no or limited amount of data from the use of cholecalciferol (vitamin D₃) in pregnant women. Studies in animals have shown reproductive toxicity (see section 5.3 Preclinical safety data). The recommended daily intake for pregnant women is 400 IU, however, in women who are considered to be vitamin D3 deficient a higher dose may be required (up to 2000 IU/day- 10 drops with the oral drops presentation). During pregnancy women should follow the advice of their medical practitioner as their requirements may vary depending on the severity of their disease and their response to treatment vitamin D3 and its metabolites are excreted in breast milk.

Breast-feeding

Vitamin D3 can be prescribed while the patient is breast-feeding if necessary. This supplementation does not replace the administration of vitamin D3 in the neonate.

Overdose in infants induced by nursing mothers has not been observed, however, when prescribing additional vitamin D3 to a breast-fed child the practitioner should consider the dose of any additional vitamin D3 given to the mother.

4.7 Effects on ability to drive and use machines

There are no data on the effects of DELTIUS on the ability to drive. However, an effect on this ability is unlikely.

4.8 Undesirable effects

Adverse reactions are listed below, by system organ class and frequency. Frequencies are defined as: uncommon (>1/1,000, <1/100) or rare (>1/10,000, <1/1,000).

Metabolism and nutrition disorders Uncommon: Hypercalcaemia and hypercalciuria Skin and subcutaneous disorders:

Rare: pruritus, rash, and urticaria.

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard

4.9 Overdose

Discontinue DELTIUS when calcaemia exceeds 10.6 mg/dl (2.65 mmol/l) or if the calciuria exceeds 300 mg/24 hours in adults or 4-6 mg/kg/day in children. An overdose manifests as hypercalcaemia and hypercalciuria, the symptoms of which include the following: nausea, vomiting, thirst, constipation, polyuria, polydipsia and dehydration.

Chronic overdosage may lead to vascular and organ calcification, as a result of hypercalcaemia.

Treatment in cases of overdose

Discontinue administration of DELTIUS and initiate rehydration.

5. PHARMACOLOGICAL PROPERTIES

5.1 Pharmacodynamic properties

Pharmacotherapeutic group: vitamin D3 and analogues, cholecalciferol ATC Code: A11CC05

In its biologically active form vitamin D3 stimulates intestinal calcium absorption, incorporation of calcium into the osteoid, and release of calcium from bone tissue. In the small intestine it promotes rapid and delayed calcium uptake. The passive and active transport of phosphate is also stimulated. In the kidney, it inhibits the excretion of calcium and phosphate by promoting tubular resorption. The production of parathyroid hormone (PTH) in the parathyroids is inhibited directly by the biologically active form of vitamin D₃. PTH secretion is inhibited additionally by the increased calcium uptake in the small intestine under the influence of biologically active vitamin D₃.

5.2 Pharmacokinetic properties

The pharmacokinetics of vitamin D3 is well known.

Absorption

Vitamin D₃ is well absorbed from the gastro-intestinal tract in the presence of bile, so the administration with the major meal of the day might therefore facilitate the absorption of vitamin D₃.

Distribution and biotransformation

It is hydroxylated in the liver to form 25-hydroxy-cholecalciferol and then undergoes further hydroxylation in the kidney to form the active metabolite 1,25-dihydroxy-cholecal ciferol (calcitriol).

Elimination

The metabolites circulate in the blood bound to a specific a — globin, vitamin D3 and its metabolites are excreted mainly in the bile and faeces.

Characteristics in Specific Groups of Subjects or Patients

A 57% lower metabolic clearance rate is reported in subjects with renal impairment as compared with that of healthy volunteers.

Decreased absorption and increased elimination of vitamin D₃ occurs in subjects with malabsorption.

Obese subjects are less able to maintain vitamin D₃ levels with sun exposure, and are likely to require larger oral doses of vitamin D₃ to replace deficits.

5.3 Preclinical safety data

Pre-clinical studies conducted in various animal species have demonstrated that toxic effects occur in animals at doses much higher than those required for therapeutic use in humans.

In toxicity studies at repeated doses, the effects most commonly reported were increased calciuria and decreased phosphaturia and proteinuria.

Hypercalcaemia has been reported in high doses. In a state of prolonged hypercalcaemia, histological alterations (calcification) were more frequently borne by the kidneys, heart, aorta, testes, thymus and intestinal mucosa. Cholecalciferol (vitamin D3) has been shown to be teratogenic at high doses in animals.

At doses equivalent to those used therapeutically, cholecalciferol (vitamin D₃) has no teratogenic activity.

Cholecalciferol (vitamin D3) has no potential mutagenic or carcinogenic activity.

6 PHARMACEUTICAL PARTICULARS

6.1 List of excipients

Refined olive oil.

6.2 Incompatibilities

In absence of compatibility studies, this medicinal product must not be mixed with other medicinal products.

6.3 Shelf life

4 years.

6.4 Special precautions for storage

Do not store above 30° C.

Do not freeze or refrigerate

Keep the bottle in the outer carton in order to protect from light.

6.5 Nature and contents of container

Amber glass Type III bottle of 20 ml containing 10 ml of oral drops solution (corresponding to 500 drops), sealed by a childproof polypropylene cap.

1 dropper applicator cap with a colourless type III glass stem and polypropylene cap is provided Each pack contains 1 bottle and 1 dropper applicator cap.

6.6 Special precautions for disposal and other handling

You should preferably take DELTIUS together with meal (see section 5.2 Pharmacokinetic properties — “Absorption”).

Do not store any product or food mixture that contains this medicine for use at a later time or a next meal (see section 4.2 Posology and method of administration).

Any unused medicinal product or waste material should be disposed of in accordance with the local requirements.

7    MARKETING AUTHORISATION HOLDER

Italfarmaco S.p.A.

Viale Fulvio Testi, 330- 20126-Milano, Italy

8    MARKETING AUTHORISATION NUMBER(S)

PL 13297/0004

9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION

27/08/2013

10 DATE OF REVISION OF THE TEXT

22/01/2015

Витамин D₃ является естественной формой витамина D, который образуется у человека в коже под действием солнечных лучей. По сравнению с витамином D₂ характеризуется на 25% более высокой активностью. Витамин D связывается со специфическим рецептором витамина D (VDR), который регулирует экспрессию многих генов, включая гены ионного канала TRPV6 (обеспечивает абсорбцию кальция в кишечнике), CALB1 (кальбиндин; обеспечивает транспорт кальция в кровеносное русло), BGLAP (остеокальцин; обеспечивает минерализацию костной ткани и гомеостаз кальция), SPP1 (остеопонтин; регулирует миграцию остеокластов), REN (ренин; обеспечивает регуляцию АД, являясь ключевым элементом регуляции РААС), IGFBP (связывающий белок ИФР; усиливает действие ИФР), FGF23 и FGFR23 (фактор роста фибробластов 23; регулируют уровни кальция, фосфат-аниона, процессы клеточного деления фибробластов), TGFB1 (трансформирующий фактор роста бета-1; регулирует процессы клеточного деления и дифференцировки остеоцитов, хондроцитов, фибробластов и кератиноцитов), LRP2 (ЛПНП-рецепторсвязанный белок 2; является посредником эндоцитоза ЛПНП), INSR (рецептор инсулина; обеспечивает эффекты инсулина на любые типы клеток).

Витамин D₃ является активным антирахитическим фактором. Самая важная функция витамина D₃ — регулирование метаболизма кальция и фосфатов, что способствует правильной минерализации и росту скелета. Колекальциферол играет существенную роль в абсорбции кальция и фосфатов в кишечнике, транспорте минеральных солей и процессе кальцификации костей, регулирует также выведение кальция и фосфатов почками.

Концентрация ионов кальция в крови обусловливает поддержание тонуса мышц скелетной мускулатуры, функцию миокарда, способствует проведению нервного возбуждения, регулирует процесс свертывания крови.

Недостаток витамина D в пище, нарушение его всасывания, дефицит кальция, а также недостаточное пребывание на солнце в период быстрого роста ребенка приводит к рахиту, у взрослых — к остеомаляции, у беременных могут возникнуть симптомы тетании, нарушение процессов обызвествления костей новорожденных.

Повышенная потребность в витамине D возникает у женщин в период менопаузы, поскольку у них часто развивается остеопороз в связи с гормональными нарушениями.

Витамин D обладает рядом т.н. внескелетных эффектов.

Витамин D участвует в функционировании иммунной системы путем модуляции уровней цитокинов и регулирует деление лимфоцитов Т-хелперов и дифференцировку В-лимфоцитов. В ряде исследований отмечено снижение заболеваемости инфекциями дыхательных путей на фоне приема витамина D.

Показано, что витамин D является важным звеном гомеостаза иммунной системы: предотвращает аутоиммунные заболевания (в т.ч. сахарный диабет типа 1, рассеянный склероз, ревматоидный артрит, воспалительные болезни кишечника). Витамин D обладает антипролиферативным и продифференцирующим эффектами, которые обусловливают онкопротективное действие витамина D. Отмечено, что частота некоторых опухолей (рак молочной железы, рак толстого кишечника) повышается на фоне низкого уровня витамина D в крови.

Витамин D участвует в регуляции углеводного и жирового метаболизма путем влияния на синтез IRS1 (субстрат рецептора инсулина 1; участвует во внутриклеточных путях проведения сигнала рецептора инсулина), IGF (ИФР; регулирует баланс жировой и мышечной ткани), PPAR-δ (активированный рецептор пролифераторов пероксисом, тип δ; способствует переработке избыточного Хс). По данным эпидемиологических исследований, дефицит витамина D ассоциирован с риском метаболических нарушений (метаболический синдром и сахарный диабет типа 2). Рецепторы и метаболизирующие ферменты витамина D экспрессируются в артериальных сосудах, сердце и практически всех клетках и тканях, имеющих отношение к патогенезу сердечно-сосудистых заболеваний.

На животных моделях показаны антиатеросклеротическое действие, супрессия ренина и предупреждение повреждения миокарда.

Низкие уровни витамина D у человека связаны с неблагоприятными факторами риска сердечно-сосудистой патологии, такими как сахарный диабет, дислипидемия, артериальная гипертензия, и ассоциированы с риском сердечно-сосудистых катастроф в т.ч. инсультов.

В исследованиях на экспериментальных моделях болезни Альцгеймера показано, что витамин D₃ снижал накопление амилоида в мозге и улучшая когнитивную функцию. В неинтервенционных исследованиях у человека показано, что частота развития деменции и болезни Альцгеймера увеличивается на фоне низкого уровня витамина D и низкого диетарного потребления витамина D.

Отмечалось ухудшение когнитивной функции и частоты развития болезни Альцгеймера при низких уровнях витамина D.