PATIENT INFORMATION LEAFLET
ArdineClav 875 mg/125 mg Powder for Oral Suspension in EFG Blister Packs
Read this leaflet carefully before you start taking this medicine.
Amoxicilina/Ácido clavulánico ArdineClav is an antibiotic that eliminates the bacteria that cause infections. It contains two different medications called amoxicilina and ácido clavulánico. Amoxicilina belongs to a group of medications known as “penicilinas” that sometimes may lose its effectiveness (become inactivated). The other component (ácido clavulánico) 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 the dose, administration interval, and treatment duration indicated by your doctor. Do not store or reuse this medication. If you have leftover antibiotics after treatment, return them to the pharmacy for proper disposal. Do not dispose of medications through the drain or in the trash. |
Amoxicilina/Ácido clavulánico ArdineClav is used in adults and children to treat the following infections:
Do not take Amoxicilina/Ácido clavulánico ArdineClav:
Be especially careful with Amoxicilina/Ácido clavulánico ArdineClav
Inform your doctor or pharmacist before taking this medicine if:
If you are unsure whether any of the above symptoms affect you, inform your doctor or pharmacist before taking Amoxicilina/Ácido clavulánico ArdineClav.
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 Amoxicilina/Ácido clavulánico or another medicine.
Symptoms to be aware of
Amoxicilina/Ácido clavulánico ArdineClav may worsen existing conditions or cause serious side effects. These include allergic reactions, convulsions, and inflammation of the large intestine. Be aware of certain symptoms while taking Amoxicilina/Ácido clavulánico ArdineClav to reduce the risk of problems. See “Symptoms to be aware of” 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 Amoxicilina/Ácido clavulánico ArdineClav. This is because Amoxicilina/Ácido clavulánico ArdineClav may affect the results of these types of tests.
Use of other medicines
Inform your doctor or pharmacist if you are using or have recently used other medicines, including those obtained without a prescription and herbal medicines.
If you are taking allopurinol (used for gout) with Amoxicilina/Ácido clavulánico ArdineClav, you may be more likely to suffer a skin allergic reaction.
If you are taking probenecid (used to treat gout), your doctor may adjust the dose of Amoxicilina/Ácido clavulánico ArdineClav.The concomitant use of probenecid may reduce the excretion of amoxicilina and is not recommended.
If you are taking anticoagulants (such as warfarin) with Amoxicilina/Ácido clavulánico ArdineClav, more blood tests will be required.
Amoxicilina/Ácido clavulánico ArdineClav may affect the action of methotrexate (a medicine used to treat cancer and severe psoriasis or rheumatic diseases).Penicillins may reduce the excretion of methotrexate and cause a potential increase in side effects.
Pregnancy and breastfeeding
If you are pregnant, think you may be pregnant, or are breastfeeding, speak to your doctor or pharmacist.
Consult your doctor or pharmacist before using any medicine.
Driving and operating machinery
Amoxicilina/Ácido clavulánico ArdineClav may have side effects and symptoms that may make you unable to drive.
Do not drive or operate machinery unless you feel well.
Important information about some of the components of Amoxicilina/Ácido clavulánico ArdineClav 875 mg/125 mg powder for oral suspension in sachets
This medicine contains glucose. Patients with glucose absorption problems or galactose intolerance should not take this medicine.
This medicine contains saccharose. If your doctor has told you that you have an intolerance to certain sugars, consult them before taking this medicine.
This medicine may cause tooth decay.
This medicine contains 12.50 mg of aspartamo in each sachet.
Aspartamo contains a source of phenylalanine that may be harmful in the case of phenylketonuria (PKU), a rare genetic disorder in which phenylalanine accumulates because the body is unable to eliminate it correctly.
Follow exactly the administration instructions for Amoxicilina/Ácido clavulánico ArdineClav indicated by your doctor. Consult your doctor or pharmacist if you have any doubts.
Adults and children 40 kg or more
Children under 40 kg of weight
Amoxicilina/Ácido clavulánico ArdineClav 875 mg/125 mg sachets, is not recommended.
Patients with kidney and liver problems
How to take Amoxicilina/Ácido clavulánico ArdineClav
If you take more Amoxicilina/Ácido clavulánico ArdineClav than you should
If you take too much Amoxicilina/Ácido clavulánico ArdineClav, you may experience symptoms such as stomach discomfort (nausea, vomiting, or diarrhea) or seizures. Consult your doctor as soon as possible. Bring the packaging with you to show the doctor.
You can also call the Toxicological Information Service, phone 91 562 04 20 indicating the medication and the amount taken.
If you forget to take Amoxicilina/Ácido clavulánico ArdineClav
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.
If you stop taking Amoxicilina/Ácido clavulánico ArdineClav
Continue taking Amoxicilina/Ácido clavulánico ArdineClav until you complete the treatment, even if you feel better. You need to take the full treatment to cure the infection. If you do not, the surviving bacteria may cause the infection to return.
If you have any other doubts about the use of this product, ask your doctor or pharmacist.
Symptoms to be aware of
Allergic reactions:
Colitis:
Colitis, which causes watery diarrhea, usually with blood and mucus, stomach pain, and/or fever.
Very common side effects
May affect more than 1 in 10 patients
Common side effects
May affect up to 1 in 10 patients
Uncommon side effects
May affect 1 in 100 patients
Side effects that may appear in blood tests:
Rare side effects
May affect up to 1 in 1,000 patients
Side effects that may appear in blood tests:
Other side effects
Other side effects that have occurred in a very small number of patients and whose exact frequency is unknown:
If you have intense and persistent pain in the stomach area, this could be a sign of acute pancreatitis.
Side effects that may appear in blood or urine tests:
If you have side effects
Reporting side effects
If you experience any type of side effect, consult your doctor, pharmacist, or nurse, even if it is a possible side effect not listed in this leaflet. You can also report them directly through the Spanish System for the 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 medication.
Keep out of the reach and sight of children.
Do not use Amoxicillin/Clavulanate ArdineClav after the expiration date shown on the packaging. The expiration date is the last day of the month indicated.
Do not use Amoxicillin/Clavulanate ArdineClav if the packets are torn or damaged.
Medicines should not be disposed of through drains or in the trash. Dispose of the packaging and unused medicines at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of unused packaging and medicines. By doing so, you will help protect the environment.
The active principles are Amoxicilina and Acido clavulánico. Each sachet contains:
Amoxicilina (as amoxicilina trihydrate) 875 mg
Ácido clavulánico (as clavulanate potassium) 125 mg
The other components (excipients) are: Aspartamo (E-951) and orange flavoring (contains corn-derived glucose, sucrose, and cornstarch).
Appearance of the product and contents of the package
White to off-white powder.
Packages of 20, 30, and 500 sachets
Marketing authorization holder and responsible manufacturer
Marketing authorization holder:
Reig Jofré, S.A Laboratory
Gran Capitán, 10, 08970 Sant Joan Despí (Barcelona)
Responsible manufacturer:
Reig Jofré, S.A Laboratory
C/Jarama 111. Industrial Park
45007 Toledo
This leaflet was revised in January 2023
The detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es
Instructions for reconstitution
Empty the contents of the sachet into 10-20 ml of water, shake until a suspension is obtained, and take immediately.
Есть вопросы по этому лекарству или вашим симптомам? Свяжитесь с лицензированным врачом для получения помощи и персонализированного ухода.