Concor 10(Emconcor 10 mg)
Bisoprolol fumarate
Concor 10 and Emconcor 10 mg are different trade names for the same medicine.
The active substance of Concor 10 is bisoprolol fumarate. Bisoprolol belongs to a group of medicines called beta-blockers. These medicines affect the body's response to certain nerve impulses, especially in the heart. As a result, bisoprolol slows down the heart rate and increases the efficiency of the heart in pumping blood throughout the body. Bisoprolol in doses of 5 mg and 10 mg lowers high blood pressure.
Concor 10 is used to treat high blood pressure or coronary heart disease (chest pain caused by insufficient blood supply to the heart) .
Do not take Concor 10 in the following cases:
If you experience any of the following conditions, you should discuss them with your doctor before starting Concor 10; your doctor may decide that special caution is necessary (e.g., additional medication or more frequent check-ups):
In addition, you should tell your doctor if you are planning:
Concor 10 is not recommended for use in children and adolescents.
You should tell your doctor about all medicines you are currently taking or have recently taken, as well as any medicines you plan to take.
Do not take the following medicines with Concor 10 without special recommendation by your doctor:
Before taking the following medicines with Concor 10, you should discuss them with your doctor; your doctor may recommend more frequent medical check-ups:
There is a risk that taking Concor 10 during pregnancy may harm the baby.
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a baby, you should consult your doctor or pharmacist before taking this medicine. Your doctor will decide whether you can take Concor 10 during pregnancy.
It is not known whether bisoprolol passes into human milk, so breastfeeding is not recommended during treatment with Concor 10.
The medicine, depending on how it is tolerated, may impair the ability to drive or operate machines. You should be particularly careful at the beginning of treatment, after increasing the dose, or when changing medicines, as well as when combining the medicine with alcohol.
This medicine should always be taken as directed by your doctor. If you have any doubts, you should consult your doctor or pharmacist.
During treatment with Concor 10, regular medical check-ups are necessary. This is especially important at the beginning of treatment, during dose increase, and in case of treatment discontinuation.
The tablet should be taken in the morning with food or independently of food, washed down with water. The tablets should not be crushed or chewed.
Concor 5 (5 mg) and Concor 10 (10 mg) are available on the market.
In both indications, the usual dose is one Concor 5 tablet or 1/2 Concor 10 tablet (equivalent to 5 mg bisoprolol fumarate) once a day.
If necessary, your doctor may increase the dose to one Concor 10 mg tablet or two Concor 5 mg tablets (equivalent to 10 mg bisoprolol fumarate) once a day.
The maximum recommended dose is 20 mg once a day.
In patients with mild to moderate liver or kidney impairment, there is usually no need to modify the dosage. In patients with severe renal or hepatic impairment, a dose greater than 10 mg bisoprolol per day should not be used.
Experience with bisoprolol in patients undergoing dialysis is limited; however, there is no evidence that dosage modification is necessary.
Dose adjustment is not necessary.
Concor 10 is not recommended for use in children and adolescents.
Treatment with Concor 10 is usually long-term.
If treatment needs to be discontinued, your doctor will usually recommend gradual reduction of the dose, otherwise the disease may worsen.
If you have taken a higher dose of Concor 10 than recommended, you should immediately inform your doctor. Your doctor will decide what actions to take.
Symptoms of overdose include: slow heart rate, difficulty breathing, significant drop in blood pressure, dizziness, or seizures (caused by decreased blood sugar levels).
You should not take a double dose to make up for a missed dose. The next morning, you should take the recommended dose.
You should never stop taking Concor 10 unless your doctor recommends it. Otherwise, the disease may worsen.
If you have any further doubts about taking this medicine, you should consult your doctor or pharmacist.
Like all medicines, Concor 10 can cause side effects, although not everybody gets them.
Frequent(occurring in less than 1 in 10 patients)
* These symptoms occur mainly at the beginning of treatment. They are usually mild and disappear within 1-2 weeks.
Uncommon(occurring in less than 1 in 100 patients)
Rare(occurring in less than 1 in 1000 patients)
Very rare(occurring in less than 1 in 10,000 patients):
If you experience any side effects, including any side effects not listed in this leaflet, you should tell your doctor or pharmacist. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products 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
website: https://smz.ezdrowie.gov.pl.
By reporting side effects, you can help gather more information 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 packaging. The expiry date refers to the last day of the month.
Do not store above 30°C.
Medicines should not be disposed of via wastewater or household waste. You should ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
tablet core: silicon dioxide, magnesium stearate, crospovidone, microcrystalline cellulose, corn starch, calcium hydrogen phosphate;
tablet coating: yellow iron oxide (E 172), red iron oxide (E 172), dimeticone, macrogol 400, titanium dioxide (E 171), hypromellose.
Concor 10 mg has the form of light orange/orange tablets in the shape of a heart, with a dividing line.
PVC-Al blisters in a cardboard box.
Each pack contains 30 coated tablets.
For more detailed information, you should contact the marketing authorization holder or the parallel importer.
Merck, S.L.
María de Molina, 40
28006 Madrid
Spain
MERCK, S.L.
Polígono Merck
08100 Mollet del Vallés (Barcelona)
Spain
Merck KgaA
Frankfurter Strasse 250
D-64293 Darmstadt
Germany
InPharm Sp. z o.o.
ul. Strumykowa 28/11
03-138 Warsaw
InPharm Sp. z o.o. Services sp. k.
ul. Chełmżyńska 249
04-458 Warsaw
Spanish marketing authorization number, country of export:978114.9
Parallel import authorization number:278/09
[Information about the trademark]
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