Amoksiklav 1000 mg is an antibiotic that kills bacteria that cause infections.
It contains two different medicines: amoxicillin and clavulanic acid. Amoxicillin belongs to a group of medicines called penicillins, which can sometimes be inactivated (inhibited).
The second active substance (clavulanic acid) counteracts this inactivation.
Amoksiklav 1000 mg is used in adults and children to treat the following infections:
middle ear and sinus infections,
respiratory tract infections,
urinary tract infections,
skin and soft tissue infections, including dental infections,
bone and joint infections.
if you are allergic (hypersensitive) to amoxicillin, clavulanic acid, penicillin or any of the other ingredients of this medicine (listed in section 6);
if you have ever had a severe allergic reaction (hypersensitivity) to any other antibiotic; such a reaction may include a skin rash, swelling of the face or neck;
if you have ever had liver function disorders or jaundice (yellowing of the skin), caused by taking an antibiotic.
Amoksiklav 1000 mg.If you are unsure before taking Amoksiklav 1000 mg, consult your doctor or pharmacist.
Before taking this medicine, discuss it with your doctor or pharmacist if you:
have infectious mononucleosis
are being treated for liver or kidney disorders
do not urinate regularly.
If you are unsure whether any of these statements apply to you, consult your doctor or pharmacist before taking the medicine.
In some cases, your doctor may test what type of bacteria caused the infection. Depending on the test results, you may be given Amoksiklav of a different strength or a different medicine.
Taking Amoksiklav 1000 mg may worsen the course of some existing diseases or cause severe side effects (such as allergic reactions, seizures and colitis). To minimize the risk of any problems, while taking Amoksiklav 1000 mg, you should pay attention to whether certain symptoms occur (see "Conditions to watch out for" in section 4).
If you are going to have a blood test (e.g. red blood cell test or liver function tests) or a urine test (for glucose), tell your doctor or nurse that you are taking Amoksiklav 1000 mg. The medicine may affect the results of these tests.
Tell your doctor or pharmacist about all the medicines you are taking now or have recently taken, as well as the medicines you plan to take, including those that are available without a prescription and herbal medicines.
If you are taking allopurinol (used to treat gout) at the same time as Amoksiklav 1000 mg, the likelihood of a skin allergic reaction increases.
If you are taking probenecid (used to treat gout), your doctor may decide to modify the dose of Amoksiklav 1000 mg. Taking probenecid at the same time may reduce the excretion of amoxicillin and is not recommended.
If you are taking medicines that reduce blood clotting (such as warfarin) with Amoksiklav 1000 mg, you may need to have additional blood tests.
Amoksiklav 1000 mg may affect the action of methotrexate (a medicine used to treat cancer and severe psoriasis). Penicillins may reduce the excretion of methotrexate, potentially leading to increased side effects.
If you are receiving mycophenolate mofetil (a medicine used to prevent organ rejection), while taking Amoksiklav 1000 mg, your doctor will closely monitor your health.
If you are pregnant or breastfeeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Amoksiklav 1000 mg may cause side effects and symptoms that disrupt the ability to drive vehicles. Do not drive vehicles or operate machinery unless you feel well.
The medicine contains sulfites (a component of the orange flavor). The medicine can rarely cause severe hypersensitivity reactions and bronchospasm.
The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means that the medicine is considered "sodium-free".
Always take this medicine exactly as your doctor has told you. If you are unsure, ask your doctor or pharmacist.
Usual dose: 1 tablet twice a day
Larger dose: 1 tablet three times a day
Children under 6 years of age should preferably receive Amoksiklav in the form of an oral suspension.
Before taking Amoksiklav 1000 mg tablets in children with a body weight of less than 40 kg, consult a doctor or pharmacist.
For patients with impaired renal function, the dose may be changed. Your doctor may prescribe a different strength of Amoksiklav or a different medicine.
Patients with impaired liver function may need to have blood tests more frequently to monitor liver function.
Take the tablet at the beginning of a meal or just before a meal.
Keep equal, at least 4-hour, intervals between doses given during the day. Do not take 2 doses within 1 hour.
Do not take Amoksiklav 1000 mg for longer than 2 weeks. If you still feel unwell, consult your doctor again.
The tablet can be mixed thoroughly with half a glass of water.
If you have taken a higher dose of Amoksiklav 1000 mg than recommended, you may experience symptoms such as stomach and intestinal irritation (nausea, vomiting, or diarrhea) or seizures.
Contact your doctor as soon as possible. Take the medicine packaging with you to show the doctor.
If you forget to take a dose, take it as soon as you remember. Do not take the next dose too soon, but wait about 4 hours before taking it.
Take Amoksiklav 1000 mg until the end of the treatment, even if you feel better.
To combat the infection, all doses of the medicine are needed. If some bacteria survive, they may cause a relapse of the infection.
If you have any further questions about taking this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
skin rash
vasculitis, which can appear as red or purple raised spots on the skin, but can also affect other parts of the body
fever, joint pain, swelling of lymph nodes in the neck, armpit or groin
swelling, sometimes of the face or mouth (angioedema), causing difficulty breathing
fainting
chest pain associated with an allergic reaction, which can be a sign of an allergy leading to a heart attack (Kounis syndrome).
Colitis, causing watery diarrhea, usually with blood and mucus, stomach pain and (or) fever.
If you experience severe and persistent stomach pain, it may be a sign of acute pancreatitis.
Drug-induced enterocolitis syndrome occurred mainly in children receiving amoxicillin with clavulanic acid. It is a type of allergic reaction, the leading symptom of which is repeated vomiting (1 to 4 hours after taking the medicine). Further symptoms may include abdominal pain, lethargy, diarrhea, and low blood pressure.
Very common side effects(more than 1 in 10 people)
diarrhea
Common side effects(less than 1 in 10 people)
candidiasis - fungal infection of the vagina, mouth (thrush) or skin folds
nausea, especially when taking high doses of the medicine.
→ If you experience nausea, take Amoksiklav 1000 mg before eating.
vomiting
Uncommon side effects(less than 1 in 100 people)
skin rash, itching
raised, itchy rash (hives)
indigestion
dizziness
headache
Uncommon side effects that may appear in blood test results:
increased activity of certain substances (enzymes) produced in the liver
Rare side effects(less than 1 in 1000 people)
skin rash that can change into blisters and looks like small targets (dark spot in the center surrounded by a lighter border with a dark edge - erythema multiforme)
Rare side effects that may appear in blood test results:
low number of blood cells involved in blood clotting
low number of white blood cells
Other side effects have occurred in a very small number of people, but their exact frequency is not known.
allergic reactions (see above)
colitis (see above)
severe skin reactions:
liver inflammation
jaundice due to increased bilirubin levels in the blood, which can cause yellowing of the skin and whites of the eyes
interstitial nephritis
prolonged blood clotting time
restlessness
seizures (in people taking high doses of Amoksiklav 1000 mg or with kidney disease)
black hairy tongue, which looks like a hairy tongue
development of an infection caused by excessive growth of non-susceptible bacteria
Side effects that may appear in blood or urine test results:
significant decrease in the number of white blood cells
low number of red blood cells (hemolytic anemia)
crystals in the urine
If you experience any side effects, including those not listed in this leaflet, please tell your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products:
Al. Jerozolimskie 181C, 02-222 Warsaw
Phone: +48 22 49 21 301
Fax: +48 22 49 21 309
website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
Reporting side effects will help to gather more information on the safety of this medicine.
Keep the medicine out of the sight and reach of children.
Do not store above 25°C. Store in the original packaging to protect from moisture.
Do not use this medicine after the expiry date stated on the packaging after EXP.
The expiry date refers to the last day of the month stated.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
The active substances are amoxicillin and clavulanic acid.
One tablet contains 875 mg of amoxicillin in the form of amoxicillin trihydrate and 125 mg of clavulanic acid in the form of potassium clavulanate. Each tablet contains 25 mg of potassium.
The other ingredients are: crospovidone, sucralose, magnesium stearate, silicon dioxide, yellow iron oxide (E172), microcrystalline cellulose silicified (microcrystalline cellulose and silicon dioxide), orange flavor (contains propylene glycol, sodium, sulfites (as SO2)).
The tablets are oval, yellow-brown, speckled, approximately 13 x 25 mm in size.
They are packaged in blisters containing 14 tablets.
Sandoz GmbH
Biochemiestrasse 10
A-6250 Kundl, Austria
To obtain more detailed information about this medicine, contact the representative of the marketing authorization holder:
Sandoz Polska Sp. z o.o.
ul. Domaniewska 50 C
02-672 Warsaw
phone: +48 22 209 70 00
(logo of the marketing authorization holder)
Antibiotics are used to treat bacterial infections. They are ineffective in treating viral infections.
Sometimes bacterial infections do not respond to antibiotic treatment.
One of the most common reasons for this phenomenon is that bacteria are resistant to the administered antibiotic.
This means that bacteria can survive or multiply despite the use of an antibiotic.
Bacteria can become resistant to antibiotics for many reasons. Careful use of antibiotics can help reduce the possibility of bacteria developing resistance.
The antibiotic prescribed by your doctor is intended solely for the treatment of the current disease. Paying attention to the following tips will help prevent the development of resistant bacteria that could hinder the action of the antibiotic.
Need help understanding this medicine or your symptoms? Online doctors can answer your questions and offer guidance.