Package Leaflet: Information for the User
Clamoxyl 1 g Dispersible Tablets
amoxicillin
Read this package leaflet carefully before you start taking this medicine because it contains important information for you.
What is Clamoxyl
Clamoxyl is an antibiotic. The active ingredient is amoxicillin. This belongs to a group of medicines called “penicillins”.
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 any leftover antibiotic after treatment, return it to the pharmacy for proper disposal. Do not dispose of the medication through the drain or in the trash. |
What is Clamoxyl used for
Clamoxyl is used to treat bacterial infections in different parts of the body. Clamoxyl can also be used in combination with other medications to treat stomach ulcers.
Do not take Clamoxyl if any of the above points apply to you. If you are unsure, consult your doctor or pharmacist before taking Clamoxyl.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Clamoxyl if:
If you are unsure whether any of the above symptoms apply to you, consult your doctor or pharmacist before taking Clamoxyl.
Blood and urine tests
If you are having:
Inform your doctor or pharmacist that you are taking Clamoxyl. This is because Clamoxyl may affect the results of these types of tests.
Other medications and Clamoxyl
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medication.
Driving and operating machinery
Clamoxyl may have adverse effects and symptoms (such as allergic reactions, dizziness, and seizures) that may make you unfit to drive.
Do not drive or operate machinery unless you are feeling well.
Clamoxyl 1 g dispersible tablets contain aspartame
This medication contains 20 mg of aspartame in each dispersible tablet. Aspartame contains a source of phenylalanine that may be harmful if you have phenylketonuria (PKU), a rare genetic disorder in which phenylalanine accumulates because the body is unable to eliminate it correctly.
uniformly. Swallow the mixture immediately.
The usual dose is:
Children under 40 kg in weight
All doses are calculated based on the child's body weight in kilograms.
Adults and children 40 kg or more in weight
The usual dose of Clamoxyl is 250 mg to 500 mg three times a day or 750 mg to 1 g every 12 hours, depending on the severity and type of infection.
Renal problems
If you have renal problems, the dose may be lower than the usual dose.
If you take more Clamoxyl than you should
If you have taken more Clamoxyl than you should, the signs may be stomach discomfort (nausea, vomiting, or diarrhea) or crystals in the urine, which may be observed as cloudy urine, or difficulty urinating. Talk to your doctor as soon as possible. Bring the medication to show it to your 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.
If you forgot to take Clamoxyl
How long should you take Clamoxyl
Candidiasis (a fungal infection of the moist parts of the body that can cause pain, itching, and white discharge) may appear if you take Clamoxyl for a prolonged period. If this happens, consult your doctor.
If you take Clamoxyl for a prolonged period, your doctor may perform additional tests to check that your kidneys, liver, and blood are functioning normally.
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
Stop taking Clamoxyl and see a doctor immediately if you experience any of the following severe side effects – you may need urgent medical treatment:
The following side effects are very rare (may affect up to 1 in 10,000 people).
These may occur during treatment or several weeks after.
The following side effects are not known (frequency cannot be estimated from available data)
If any of the above symptoms appear, stop taking the medication and see your doctor immediately.
Occasionally, you may experience milder skin reactions, such as:
If you experience any of them, talk to your doctor as you may need to interrupt your Clamoxyl treatment.
Other possible side effects are:
Frequent(may affect up to 1 in 10 people)
Rare(may affect up to 1 in 100 people)
Very rare(may affect up to 1 in 10,000 people)
Not known(frequency cannot be estimated from available data)
Reporting of 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 the Pharmacovigilance of Medicines for Human Use:www.notificaRAM.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging, after CAD. The expiration date is the last day of the month indicated.
Do not store at a temperature above 25°C.
Do not use this medication if you observe visible signs of deterioration.
Medications should not be disposed of through drains or in the trash. Deposit the containers and medications you no longer need at the SIGRE collection point of the pharmacy. If in doubt, ask your pharmacist how to dispose of the containers and medications you no longer need.By doing so, you will help protect the environment.
C omposition of Clamoxyl
Appearance of the product and content of the packaging
Clamoxyl 1 g dispersible tablets are oval-shaped, white to off-white tablets with a notch, and marked with “1 g”. The notch is only for breaking the tablet, to make it easier to swallow, but not for dividing into equal doses.
They are packaged in blisters, in a case. It is available in packaging sizes of 6, 8, 12, 14, 16, 18, 20, 24, 30, and in a clinical pack of 100 tablets.
Only some packaging sizes may be commercially available.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization
GlaxoSmithKline, S.A.
P.T.M. C/ Severo Ochoa, 2
28760 Tres Cantos (Madrid)
Tel: +34 900 202 700
Responsible for manufacturing
Glaxo Wellcome Production
Z.I. de la Peyennière
53100 Mayenne, France
This medicine is authorized in the member states of the European Economic Area with the following names:
Belgium – Clamoxyl
France – Clamoxyl, Amoxiciline Biogaran
Greece – Amoxil
Luxembourg – Clamoxyl
Portugal – Clamoxyl
Spain – Clamoxyl
Date of the last review of this leaflet : April 2024
The detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) (http://www.aemps.gob.es/)
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