AMOKSIKLAV 375 mg. 15 tablets
What is the active substance?
1 tablet Amoksiklav 375 mg contains 250 mg amoxicillin, as amoxicillin trihydrate, and 125 mg clavulanic acid, in the form of potassium clavulanate
What else contain Amoksiklav film?
1 tablet contains 375 mg Amoksiklav anhydrous colloidal silicon dioxide, crospovidone, croscarmellose sodium, magnesium stearate, talc, microcrystalline cellulose, hydroxypropyl cellulose, ethyl cellulose, polysorbate, triethyl citrate, titanium dioxide (E 171), talc.
Formulation and packaging:
Original package containing a vial of 15 or 21 tablets and desiccant (moisture-).
What is Amoksiklav film?
Amoksiklav is an antibiotic to treat infections. It belongs to a class of antibiotics called beta-lactam penicillins. Bactericidal works by destroying the bacteria causing the infection. There is a wide antibacterial spectrum of action.
Name of the medicinal product:
What is Amoksiklav film?
For treatment of the following infections sensitive Amoksiklav:
♦ infections of the upper respiratory tract (acute bacterial and exacerbated inflammation of the paranasal sinuses (sinusitis), acute and chronic inflammation of the middle ear (otitis media), paranasal abscess (abscesses)
♦ infections of the lower respiratory tract (chronic bronchitis, pneumonia)
♦ urinary tract infections
♦ gynecological infections
♦ bite from an animal or person
♦ infections of skin and soft tissue
- Infections of the bones and connective tissue
♦ cholecystitis and cholangitis (inflammation of the gallbladder)
♦ soft chancre
♦ odontogenic infections (infections in the mouth, teeth)
♦ abdominal infections
♦ treatment of mixed infections caused by Gram-negative and Gram-positive organisms and anaerobes
BEFORE USING AMOKSIKLAV
When you should not take Amoksiklav film?
Amoksiklav should not apply if:
♦ have an allergy to Amoksiklav or any of the other ingredients of the product (active or excipient)
♦ have an allergy to penicillin antibiotics
An allergic reaction while using the drug usually characterized by skin rashes, swelling of the face, neck or throat, difficulty in breathing.
♦ have or have had cholestatic jaundice or hepatic dysfunction due to use of penicillins or combination amoxicillin / clavulanic acid
What special precautions should be followed when administering Amoksiklav® film?
♦ If you have severe kidney or liver, your doctor will adjust the dose or prolong the intervals between doses
♦ if you suffer from infectious mononucleosis (swollen lymph glands) or lymphocytic leukemia
♦ if you are allergic to beta-lactam antibiotics
♦ If you have severe diarrhea with antibiotics, you should tell your doctor. It is possible in almost all antibiotics appear pseudomembranous colitis, which can range from mild to life-zastashavasht.
During treatment, it is important to drink plenty of fluids to prevent the risk of crystalluria (formation of crystals in the urine.
Please tell your doctor if you have had some of the past.
What special precautions should be taken during pregnancy and lactation?
Talk to your doctor or pharmacist before taking any lekarstva.Neobhodimo is to inform your doctor if you are pregnant (or you suspect you are) or karmite.Nyama evidence of harmful (teratogenic) effects on the fetus. Amoksiklav can be used during pregnancy only if absolutely necessary. Only a small amount of Amoksiklav are excreted in breast milk, because caution is required for use in lactating women.
What to be aware when driving, operating machinery or in a precarious situation (eg. Climbing stairs)?
The drug does not affect mental and / or physical abilities.
Important information about ingredients of Amoksiklav:
The film-coated tablets contain potassium, which can be harmful to patients on a restricted diet of potassium (hyperkalemia causes). Oral administration can be accompanied by gastrointestinal disorders.
What other products influence the effect of Amoksiklav tablets or can be influenced by product?
Please tell your doctor if you are taking any other medicines, even if no retsepta.Informirayte doctor if you are taking methotrexate, since concomitant use of methotrexate and Amoksiklav increases the toxicity of metotreksata.Ednovremennoto use with allopurinol increases the frequency of the occurrence of skin with obriv.Amoksiklav aminoglycosides
Tablets are not suitable for children below 40 kg body weight.
What should I do if Amoksiklav film was adopted in very large quantities (intentional or inadvertent overdose)?
If you take more tablets than expected at once, immediately consult your doctor. Show the doctor the package with the remainder tabletki.Sled overdose in most patients no symptoms or have arisen only mild gastrointestinal symptoms such as nausea, abdominal pain, vomiting and diarrhea. Very rarely they are experiencing skin rashes, hyperactivity, headache, drowsiness or kidney inflammation (interstitial nephritis).
What should you do if you take less than the prescribed dose Amoksiklav film or you forget to take a product?
If you forget to take prescribed dose of Amoksiklav, take a dose as soon as you remember, and only if at least 4 hours until the next dose. Then continue as before (take the next dose at 8 hours). Do not take two dozi.Ne stop taking Amoksiklav® tablets earlier than prescribed by your doctor, even if you feel better.If stop treatment before the end of therapy, some of the bacteria to survive, which could to resume infection.
Tell your doctor if you still do not feel well after taking the prescribed dozi.Ako think that the effect of the drug is too strong or too weak, talk to your doctor or farmatsevt.Vie should not take more than the prescribed dose!
POSSIBLE SIDE EFFECTS
What side effects can cause the application of Amoksiklav film? Please tell your doctor or pharmacist if you experience side effects.
Like all medicines, Amoksiklav can cause adverse reactions are usually mild and transient. Most common are stomach disorders (nausea), vomiting and diarrhea. They can be reduced by taking the drug with meals or just before it. Food does not affect the action of the drug. Some patients have mycosis (fungi in the mouth, vagina or skin folds) during treatment or immediately thereafter. Talk to your doctor about pomosht.Ponyakoga Amoksiklav can cause transient changes in blood kartina.Nyakoi patients when taking Amoksiklav receive skin rash with itching. In case of rash and itching should stop taking the drug immediately and consult a doctor.
Must be immediately discontinued Amoksiklav and immediately visit a doctor or hospital in case of:
♦ swelling of the hands, ankles, face, lips, mouth and throat that may cause difficulty in swallowing or breathing
♦ collapse (fainting)
♦ yellowing of the skin or eyes (jaundice)
These are very rare but serious side effects. If you have these symptoms are likely to be allergic Amoksiklav. In that case, you need immediate medical attention or hospital admission.
Immediate medical advice in case of:
♦ severe diarrhea (caused by the occurrence of pseudomembranous colitis)
♦ darkening of the urine, lightening faeces (stools), yellowing of eyes and skin (as a result of cholestatic jaundice and inflammation of the liver - hepatitis)
♦ reduce the amount of urine compared to normal (due to kidney inflammation - interstitial nephritis)
These are very rare but serious side effects, but need medical pomosht.Ako monitor side effects not listed in this leaflet, please tell your doctor or pharmacist.
Keep out of reach of children! Store at temperatures below 25 ° C, protected from moisture. Store in the original container. Close the bottle immediately after use. Desiccant in the vial with the tablets should not be swallowed.
2 years. The drug should not be used after the expiry date stated on the packaging.