it contains important information for the patient.
THORENS oral solution contains cholecalciferol (Vitamin D). Vitamin D is found in some foods and is also produced by the body when the skin is exposed to sunlight. Vitamin D helps the body absorb calcium in the kidneys and intestines and supports bone tissue formation. A deficiency of Vitamin D is the main cause of rickets (disrupted bone mineralization in children) and osteomalacia (insufficient bone mineralization in adults). THORENS oral solution is used to treat clinically significant Vitamin D deficiency in adults.
When not to take the medicine:
Before starting to take THORENS, the patient should discuss it with their doctor or pharmacist if:
Using this medicine in children and adolescents under 18 years of age is not recommended.
The patient should inform their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take. This is especially important if the patient is taking:
This medicine is best taken during a large meal to support Vitamin D absorption by the body. To facilitate taking this medicine, the solution can be mixed with a small amount of cold or warm food. For more information, see section 3 "How to take THORENS".
If the patient is pregnant or breastfeeding, or thinks they may be pregnant, they should consult their doctor or pharmacist before taking this medicine. Using this high-strength preparation is not recommended in pregnant or breastfeeding women.
Information on the possible effect of this medicine on the ability to drive and use machines is limited. However, it is unlikely that this medicine will affect the ability to drive and use machines.
This medicine should always be taken according to the doctor's or pharmacist's recommendations. In case of doubts, the patient should consult their doctor or pharmacist. Before use, shake the bottle. THORENS is best taken during a meal. This medicine has the taste of olive oil. It can be taken in its original form, directly from the bottle, or mixed with a small amount of cold or warm food immediately before administration. The patient should ensure that the entire dose of the medicine is taken.
The recommended dose is 1 bottle once a week for the first month of treatment, and then the dose will be determined by the doctor.
Using THORENS 25,000 IU in children and adolescents under 18 years of age is not recommended.
Using THORENS 25,000 IU is not recommended in pregnant or breastfeeding women.
In case of taking a higher dose of the medicine than prescribed, the patient should stop taking it and contact their doctor. If it is not possible to talk to the doctor, the patient should go to the emergency department of the nearest hospital, taking the leaflet included in the packaging of this medicine. The most common symptoms of overdose are: nausea, vomiting, increased thirst, increased urine production, constipation, and dehydration, elevated calcium levels in the blood and urine (hypercalcemia and hypercalciuria) confirmed by laboratory tests.
In case of missing a dose of THORENS, the patient should take it as soon as possible. The next dose should be taken at the usual time. However, if the time for the next dose is approaching, the patient should not take the missed dose, but only take the next dose at the usual time. The patient should not take a double dose to make up for the missed dose. In case of any further doubts related to the use of this medicine, the patient should consult their doctor or pharmacist.
Like all medicines, THORENS can cause side effects, although not everybody gets them. Possible side effects may include:
Uncommon(in less than 1 in 100 people)
Rare(in less than 1 in 1000 people)
If the patient experiences any side effects, including any side effects not mentioned in the leaflet, they should inform their doctor or pharmacist. Side effects can also be reported directly to the Department of Pharmacovigilance of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products: Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: +48 22 49 21 301, fax: +48 22 49 21 309, e-mail: ndl@urpl.gov.pl. Side effects can also be reported to the marketing authorization holder. By reporting side effects, more information can be collected on the safety of the medicine.
The medicine should be stored out of sight and reach of children. Do not use this medicine after the expiry date stated on the carton and bottle after "EXP". The expiry date refers to the last day of the month stated. Do not store above 30°C. Do not refrigerate or freeze. Store the bottle in the outer packaging to protect it from light. Do not use this medicine if the solution is discolored. Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
A single-dose bottle of 2.5 ml oral solution contains 25,000 IU of cholecalciferol (Vitamin D), which corresponds to 0.625 mg. 1 ml of oral solution contains 10,000 IU of cholecalciferol (Vitamin D), which corresponds to 0.25 mg.
THORENS 25,000 IU/2.5 ml, oral solution is a clear and colorless to greenish-yellow oily solution without visible particles and/or sediment. It is supplied in an orange glass bottle with a plastic cap. Each pack contains 1 or 4 bottles of 2.5 ml solution. Not all pack sizes may be marketed.
Italfarmaco S.p.A. Viale Fulvio Testi, 330, 20126 Milan, Italy
Abiogen Pharma S.p.A. Via Meucci, 36 – Loc. Ospedaletto, 56121 Pisa, Italy, info@abiogen.it
Sweden: Deltius 25,000 IU/2.5 ml oral solution, Norway: Deltius 25,000 I.E./2.5 ml mixture, solution, Belgium: Thorens 25,000 UI/2.5 ml, oral solution, United Kingdom: Thorens 25,000 I.U./2.5ml oral solution, Germany: Thorens 25,000 IE /2.5 ml solution for ingestion, Ireland: Thorens 25,000 I.U./2.5ml oral solution, Netherlands: Thorens 25,000 IE/2.5 ml drink, Spain: Thorens, Portugal: Thorens
Date of last revision of the leaflet:{MM/YYYY}
Detailed information about this medicine is available on the website of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products.
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