Prospecto:information for the user
Medoclav 875 mg/125 mg film-coated tablets EFG
amoxicillin/clavulanic acid
Read this prospectus carefully before starting to take this medication,because it contains important information for you.
1.What is Medoclav and what is it used for
2.What you need to knowbeforestarting totake Medoclav
3.How to take Medoclav
4.Possible adverse effects
5Storage of Medoclav
6.Contents of the package and additional information
Medoclav is an antibiotic that eliminates bacteria that cause infections. It contains two different medications called amoxicillin and clavulanic acid. Amoxicillin belongs to a group of medications known as "penicillins" that may sometimes lose their effectiveness (become inactivated). The other component (clavulanic acid) prevents this from happening.
Antibiotics are used to treat bacterial infections and do not work for viral infections such as the flu or a cold.
It is essential to follow the instructions regarding dosage, administration interval, and treatment duration as indicated by your doctor.
Do not store or reuse this medication. If you have leftover antibiotics after completing treatment, return them to the pharmacy for proper disposal. Do not dispose of medications through the drain or trash.
Medoclav is used in children and adults to treat the following infections:
Do not take Medoclav:
Do not take Medoclav if you are included in any of the above points. Before starting treatment with Medoclav, if you are unsure, consult your doctor or pharmacist.
Warnings and precautions
Consult your doctor or pharmacist before starting to takeMedoclav:
If you are unsure whether any of the above symptoms affect you, inform your doctor or pharmacist before taking Medoclav.
In some cases, your doctor may investigate the type of bacteria causing your infection. Depending on the results, they may prescribe a different presentation of amoxicillin/clavulanic acid or another medication.
Be aware of the following symptoms
Medoclav may worsen existing conditions or cause serious side effects. These include allergic reactions, seizures, and inflammation of the large intestine.
You should be aware of certain symptoms while taking Medoclav to reduce the risk of problems. See “Be aware of the following symptoms” in section 4.
Blood and urine tests
If you are having blood tests (such as red blood cell studies or liver function studies) or urine tests (to control glucose levels), inform your doctor or nurse that you are taking Medoclav. This is because Medoclav may alter the results of these types of tests.
Use of Medoclav with other medications
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
Driving and operating machinery
Medoclav may cause side effects and symptoms that may make you unable to drive.
Do not drive or operate machinery unless you feel well.
Medoclav contains soy lecithin.It should not be used in case of allergy to peanuts or soy.
This medication contains less than 1 mmol of sodium (23 mg) per tablet, that is, it is essentially "sodium-free".
Follow exactly the administration instructions of this medication as indicated by your doctor.This medicationindicated by your doctor.In case of doubt, consult your doctor or pharmacist again.
Adults and children weighing 40 kg or more
The recommended dose is:
Children weighing less than 40 kg
It is preferable to treat children 6 years old or less with oral suspension of Medoclav or the sachets.
Ask your doctor or pharmacist for advice when administering amoxicillin/clavulanic acid to children
who weigh less than 40 kg.The tablets are not suitable for children weighing less than 25 kg.
Patients with kidney and liver problems
How to take Medoclav
If you take more Medoclav than you should
If you take too much Medoclav, you may experience symptoms such as stomach upset (nausea, vomiting, or diarrhea) or convulsions. Consult your doctor as soon as possible. Bring the packaging with you to show the doctor.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately, or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested. It is recommended to bring the packaging and the medication leaflet to the healthcare professional.
If you forget to take Medoclav
If you forget to take a dose, take it as soon as you remember. Do not take the next dose too soon, wait at least 4 hours before taking the next dose. Do not take a double dose to make up for the missed doses.
If you interrupt the treatment with Medoclav
Continue taking Medoclav until you complete the treatment, even if you feel better. You need to take the complete treatment to cure the infection. If you do not, the surviving bacteria may cause you to get the infection again.
If you have any other doubts about the use of thismedication, ask your doctororpharmacist.
Like all medicines, this medicine can cause side effects, although not everyone will experience them.
Symptoms you should be aware of
Allergic reactions:
→Contact your doctor immediately if you experience any of these symptoms.Stop taking Medoclav.
Colitis:
Colitis, which causes watery diarrhea, usually with blood and mucus, stomach pain, and/or fever.
Acute pancreatitis:
If you have intense and persistent pain in the stomach area, this could be a sign of acute pancreatitis.
Drug-induced enterocolitis syndrome (DIES):
DIES has mainly been reported in children taking amoxicillin. It is a certain type of allergic reaction with the main symptom of repeated vomiting (1-4 hours after taking the medication). Other symptoms may include abdominal pain, lethargy, diarrhea, and low blood pressure.
→ Contact your doctor as soon as possible for advice, if you experience these symptoms.
Side effectsvery common(may affect more than 1 in 10 people)
Side effectscommon(may affect up to 1 in 10 people)
→ If this happens, take Medoclav with meals.
Side effectsuncommon(may affect 1 in 100 people)
Side effects that may appear in blood tests:
Side effectsrare(may affect up to 1 in 1,000 people)
→ If you experience any of these symptoms, see a doctor urgently.
Side effects that may appear in blood tests:
Frequency not known(frequency that cannot be estimated from available data).
→ Contact a doctor immediately if you experience any of these symptoms.
Side effects that may appear in blood or urine tests:
Reporting side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through the Spanish System for Pharmacovigilance of Medicines for Human Use:http://www.notificaRAM.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keepthis medicationout of the sight and reach of children.
Do not usethis medicationafter the expiration date that appears onthe boxafter
CAD. The expiration date is the last day of the month indicated.
Store at a temperature below 25°C in the original packaging to protect it from light and humidity.
Medicines should not be disposed of through drains or in the trash. Dispose of packaging and medications you no longer need at thePharmacy Take-Back Point. If in doubt, ask your pharmacisthow to disposeofpackaging and medications you no longerneed. This will help protect the environment.
Composition ofMedoclav
Tablet core: microcrystalline cellulose 105, sodium carboxymethyl starch (type A), anhydrous colloidal silica, magnesium stearate.
Coating:poly(vinyl alcohol), titanium dioxide (E 171), talc (E 553b), macrogol 4000, soy lecithin (E 322), purified water.
Appearance of the product and contents of the pack
Caplet-shaped tablets, white to off-white in color, with a core size of 21.5 mm x 10.0 mm.
Aluminum-PVC-aluminum blisters containing 2, 4, 12, 14, 16, 20, 24, or 30 tablets. Also available in hospital packs of 100 and 500 tablets.
Only some pack sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder
Medochemie Iberia, S.A.
Rua José Maria Nicolau, no6, 7oB,
1500 662 Lisboa, Portugal
Manufacturer
Medochemie LTD (Factory B)
48 Iapetou street,
Agios Athanassios Industrial Area,
4101 Agios Athanassios, Limassol
Cyprus
You can request more information about this medicine by contacting the local representative of the marketing authorization holder:
Medochemie Iberia S.A., Branch in Spain
Avenida de las Águilas, nº 2 B; 5th floor, office 6,
28044 Madrid
SPAIN
This medicine is authorized in the member states of the European Economic Area with the following names:
Czech Republic | KALVENOX |
Estonia | KALVENOX |
Greece | KALVENOX |
Portugal | ZACIVON |
Slovenia | ZACIVON |
Last review date of this leaflet: January 2023.
Medical advice/education
Antibiotics are used for the treatment of bacterial infections. They are not effective against viral infections.
Sometimes a bacterial infection does not respond to antibiotic treatment. One of the most common reasons for this is that the bacteria causing the infection are resistant to the antibiotic being taken. This means that the bacteria can survive or grow despite the antibiotic.
Bacteria can become resistant to antibiotics for many reasons. Using antibiotics properly can reduce the likelihood of bacteria becoming resistant to them.
When your doctor prescribes an antibiotic, it is only for the course of your illness. Paying attention to the following advice will help prevent the emergence of resistant bacteria that may make the antibiotic ineffective.
If you still have antibiotic left over after completing treatment, hand in all unused medicines to your pharmacy to ensure that the disposal requirements are met.
Have questions about this medication or your symptoms? Connect with a licensed doctor for guidance and personalized care.