Package Leaflet: Information for the Patient
Alcotina 20 mg Film-Coated Tablets EFG
Rosuvastatin
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack and other information
Alcotina contains the active substance rosuvastatin, which belongs to a group of medicines called statins.
You have been prescribed Alcotina because:
Heart attack, stroke, and other related health problems can be caused by a disease called atherosclerosis. Atherosclerosis is caused by the buildup of fatty deposits in your arteries.
Why it is important to keep taking Alcotina
Rosuvastatin is used to correct the levels of fatty substances in the blood called lipids, the most well-known of which is cholesterol.
There are different types of cholesterol in the blood, the "bad" cholesterol (LDL-C) and the "good" cholesterol (HDL-C).
In most people, high cholesterol levels do not affect how they feel because they do not produce any symptoms. However, if left untreated, fatty deposits can build up in the walls of blood vessels, causing them to narrow.
Sometimes, these narrowed blood vessels can become blocked, cutting off the blood supply to the heart or brain, causing a heart attack or stroke. By lowering your cholesterol levels, you can reduce your risk of having a heart attack, stroke, or related health problems.
You need to keep taking rosuvastatin, even if you have already achieved the correct cholesterol levels, because it prevents cholesterol levels from rising again and causing the buildup of fatty deposits. However, you should stop treatment if your doctor tells you to or if you become pregnant.
Do not take Alcotina
If you are taking a combination of sofosbuvir/velpatasvir/voxilaprevir
(used to treat a viral liver infection called hepatitis C).
If you are in any of the above situations (or are unsure), please consult your doctor again.
Also, do not take the highest dose (Alcotina 40 mg):
If you are in any of the above situations (or are unsure), please consult your doctor again.
Warnings and precautions
Consult your doctor or pharmacist before starting treatment with rosuvastatin
(a medicine used to treat bacterial infections), by mouth or by injection. The combination of fusidic acid and rosuvastatin can cause muscle problems (rhabdomyolysis), see "Other medicines and Alcotina".
If you are in any of these situations (or are unsure):
In a small number of people, statins can affect the liver. This is detected by a simple blood test that checks for increased levels of liver enzymes (transaminases) in the blood. For this reason, your doctor will normally do blood tests (liver function tests) before and after starting treatment with rosuvastatin.
While you are taking this medicine, your doctor will closely monitor you if you have diabetes or are at risk of developing diabetes. You are likely to be at risk of developing diabetes if you have high blood sugar levels, are overweight, and have high blood pressure.
Children and adolescents
Other medicines and Alcotina
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
Inform your doctor if you are using any of the following medicines:
-ciclosporin (used after an organ transplant),
-warfarin, ticagrelor, or clopidogrel (or any other anticoagulant, such as acenocoumarol),
-fibrates (such as gemfibrozil, fenofibrate) or any other medicine used to lower cholesterol (such as ezetimibe),
-treatments for indigestion (used to neutralize stomach acid),
-erythromycin (an antibiotic), fusidic acid (an antibiotic - see also "Warnings and precautions" and below),
-oral contraceptives (the pill),
-hormone replacement therapy
-regorafenib (used to treat cancer)
-any of the following medicines used to treat viral infections, including HIV or hepatitis C, alone or in combination (see "Warnings and precautions"): ritonavir, lopinavir, atazanavir, sofosbuvir, voxilaprevir, simeprevir, ombitasvir, paritaprevir, dasabuvir, velpatasvir, grazoprevir, elbasvir, glecaprevir, pibrentasvir.
The effects of these medicines may be altered by rosuvastatin or may change the effect of rosuvastatin.
If you need to take fusidic acid by mouth to treat a bacterial infection, you must stop taking this medicine temporarily. Your doctor will tell you when it is safe to start taking rosuvastatin again. Taking rosuvastatin with fusidic acid can rarely cause muscle weakness, tenderness, or pain (rhabdomyolysis). See more information about rhabdomyolysis in section 4.
Pregnancy and breastfeeding
Do not take rosuvastatinif you are pregnant or breastfeeding. If you become pregnant while taking rosuvastatin, stop taking it immediatelyand inform your doctor. Women should avoid becoming pregnant during treatment with rosuvastatin using an appropriate contraceptive method.
Consult your doctor or pharmacist before using any medicine.
Driving and using machines
Most patients can drive and use machines while taking rosuvastatin as it is unlikely to affect their ability. However, some people may feel dizzy while taking rosuvastatin. If you feel dizzy, consult your doctor before attempting to drive or use machines.
Alcotina contains lactose
This medicine contains lactose. If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.
Alcotina contains tartrazine (E 102) and orange yellow S (E 110)
This medicine may cause allergic reactions because it contains tartrazine (E 102) and orange yellow S (E 110). It can cause asthma, especially in patients allergic to acetylsalicylic acid.
Alcotina contains sodium
This medicine contains less than 23 mg of sodium (1 mmol) per tablet; this is essentially "sodium-free."
.
Follow the instructions for administration of this medicine exactly as told by your doctor. If in doubt, consult your doctor or pharmacist again.
Usual dose in adults
If you are taking rosuvastatin for high cholesterol:
Starting dose
Your treatment with rosuvastatin should start with a dose of 5 mg or 10 mg, even if you have taken a higher dose of another statin before. The choice of starting dose will depend on:
Check with your doctor or pharmacist what the best starting dose of rosuvastatin is for you.
Your doctor may decide to start treatment with the lowest dose (5 mg):
Increasing the dose and maximum daily dose
Your doctor may decide to increase your dose so that you are taking the right dose of rosuvastatin for you. If you started with a dose of 5 mg, your doctor may decide to double the dose to 10 mg, then to 20 mg, and later to 40 mg if necessary. If you started with a dose of 10 mg, your doctor may decide to double the dose to 20 mg and then to 40 mg if necessary. There will be an interval of four weeks between each dose adjustment.
The maximum daily dose of rosuvastatin is 40 mg. This dose is only for patients with high cholesterol and a high risk of having a heart attack or stroke, whose cholesterol levels do not decrease enough with 20 mg.
If you are taking rosuvastatin to reduce the risk of having a heart attack, stroke, or related health problems:
The recommended dose is 20 mg once daily. However, your doctor may decide to use a lower dose if you have any of the factors mentioned above.
Use in children and adolescents aged 6-17 years
The dose range in children and adolescents aged 6 to 17 years is 5 mg to 20 mg once daily. The usual starting dose is 5 mg once daily, and your doctor may gradually increase the dose to the dose of rosuvastatin that is right for you. The maximum recommended daily dose of rosuvastatin is 10 mg or 20 mg for children aged 6 to 17 years, depending on the underlying disease being treated. Take your dose once daily. Do notgive the 40 mg tablets of rosuvastatin to children.
Taking the tablets
Swallow each tablet whole with water.
Take rosuvastatin once a day.You can take it at any time of day, with or without food.
Try to take your tablets at the same time each day. This will help you remember to take them.
Regular checks of your cholesterol levels
It is important that you see your doctor regularly to have your cholesterol levels checked, to make sure that your cholesterol levels have returned to normal and are being kept at the right levels.
Your doctor may decide to increase your dose so that you are taking the right dose of rosuvastatin for you.
If you take more Alcotina than you should
Contact your doctor or the nearest hospital for advice.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, telephone 91 562 04 20, stating the medicine and the amount taken.
If you are admitted to hospital or receive treatment for another condition, inform the medical staff that you are taking rosuvastatin.
If you forget to take Alcotina
Do not worry, just take your next scheduled dose at the right time. Do not take a double dose to make up for a forgotten dose.
If you stop taking Alcotina
Consult your doctor if you want to stop taking rosuvastatin. Your cholesterol levels may rise again if you stop taking rosuvastatin.
If you have any other questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause adverse effects, although not all people suffer from them.
It is essential that you know what these adverse effects may be. They are usually mild and disappear in a short period.
Stop taking Alcotina and seek immediate medical attentionif you experience any of the following allergic reactions:
Reddish patches on the trunk, not elevated, in a target or circular shape, often with central blisters, skin peeling, ulcers in the mouth, throat, nose, genitals, and eyes. These severe skin eruptions can be preceded by fever and flu-like symptoms (Stevens-Johnson syndrome).
Also, stop taking Alcotina and consult your doctor immediately
If you experience unjustified muscle pain and crampsthat last longer than expected. Muscle symptoms are more frequent in children and adolescents than in adults. As with other statins, a very small number of people have suffered unpleasant muscle effects that, very rarely, have resulted in a potentially fatal muscle injury called rhabdomyolysis.
Common Adverse Effects (may affect up to 1 in 10 people)
Uncommon Adverse Effects (may affect up to 1 in 100 people)
Rare Adverse Effects (may affect up to 1 in 1,000 people)
Very Rare Adverse Effects (may affect up to 1 in 10,000 people)
Adverse Effects of Unknown Frequency (frequency cannot be estimated from available data) that may include:
Consult your doctor if you experience weakness in your arms or legs that worsens after periods of activity, double vision or drooping eyelids, difficulty swallowing or difficulty breathing.
Reporting Adverse Effects
If you experience any adverse effects, consult your doctor or pharmacist, even if they are possible adverse effects that do not appear in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://wwwnotificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medicine.
This medicine does not require special storage conditions.
Keep this medicine out of sight and reach of children.
Do not use this medicine after the expiration date that appears on the packaging/blister/label after CAD. The expiration date is the last day of the month indicated.
Medicines should not be thrown away through wastewater or household waste. Deposit the packaging and medicines you no longer need at the SIGRE point in the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and medicines you no longer need. This way, you will help protect the environment.
Composition of Alcotina
Core:
Calcium citrate, microcrystalline cellulose, hydroxypropylcellulose, mannitol, lactose, crospovidone, and magnesium stearate.
Coating:
Polyvinyl alcohol, titanium dioxide (E 171), macrogol 3350 (E 1521), talc, tartrazine (E 102), allura red AC (E 129), orange yellow S (E 110), and carmine indigo (E 132).
Appearance of the Product and Package Contents
Alcotina is available in packages with blisters of 28 and 30 tablets.
Alcotina 20 mg film-coated tablets are pink, oval, biconvex, and scored on one side.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder:
Industria Química y Farmacéutica VIR, S.A.
C/Laguna 66-68-70. Polígono Industrial Urtinsa II
28923 (Alcorcón) Madrid
Spain
You can request more information about this medicine by contacting the local representative of the marketing authorization holder:
ABABOR PHARMACEUTICALS, S.L.
C/ Chile 4, edificio 1, oficina 1, Las Matas,
28290, Las Rozas, Madrid.
Tel.: +34 91 630 82 75
Manufacturer:
Biofarm Sp. z o.o., ul. Walbrzyska 13, 60-198 Poznan, Poland
O
SAG Manufacturing, S.L.U., Crta. N-I, Km 36, San Agustin de Guadalix, 28750 Madrid, Spain
O
Galenicum Health, S.L., Avda. Cornellá 144, 7ª-1ª, Edificio Lekla, Esplugues de Llobregat 08950, Barcelona, Spain
Ó
Industria Química y Fca. VIR, S.A.
C/Laguna 66-68-70. P.I. Urtinsa II
28923 Alcorcón (Madrid) Spain
Date of the Last Revision of this Leaflet: May 2023
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/.
The average price of ALCOTINA 20 mg FILM-COATED TABLETS in October, 2025 is around 19.67 EUR. Prices may vary depending on the region, pharmacy, and whether a prescription is required. Always check with a local pharmacy or online source for the most accurate information.