Active ingredients: Cefixime
SUPRAX 400 mg coated tablets
SUPRAX 100mg / 5ml granules for oral suspension
SUPRAX 400 mg dispersible tablets
Indications Why is Suprax used? What is it for?
PHARMACOTHERAPEUTIC CATEGORY
Antibiotic for systemic use, belonging to the class of cephalosporins.
THERAPEUTIC INDICATIONS
SUPRAX is indicated in the treatment of infections caused by microorganisms sensitive to cefixime and in particular:
- upper respiratory tract infections (pharyngitis, tonsillitis);
- otolaryngological infections (otitis media, etc.);
- lower respiratory tract infections (pneumonia, bronchitis);
- kidney and urinary tract infections.
Contraindications When Suprax should not be used
Hypersensitivity to the active substance or to any of the excipients.
The medicine is also contraindicated in subjects with hypersensitivity to penicillins and cephalosporins (see Precautions for use).
Precautions for use What you need to know before taking Suprax
- Antibiotics are indicated only in infections of bacterial origin.
- Antibiotics, and in general all medicines, should be administered with caution to all those patients who have previously experienced allergy phenomena. It is therefore necessary to know if the patient has had any hypersensitivity reactions (allergic or "other type) in the past to cephalosporins, penicillins or other medicines, bearing in mind that it has been established that patients allergic to penicillin may also be allergic to cephalosporins ( partial cross allergenicity), and that, although rare, there have been reports of patients who have experienced anaphylactic-type reactions, especially with injectable medicines. Once SUPRAX therapy has started, the onset of any allergic-type reaction requires the suspension of the treatment.
- In patients with severe renal insufficiency, on hemodialysis or peritoneal dialysis the dosage of SUPRAX should be appropriately reduced (see Dose, Method and time of administration).
- Broad spectrum antibiotics should be administered with caution in patients with a history of gastrointestinal disease, particularly colitis.
- Antibiotics should be used at full dosage for at least 5 days before they are considered ineffective. Antibiotics should be taken at scheduled times.
Interactions Which drugs or foods may change the effect of Suprax
Tell your doctor or pharmacist if you have recently taken any other medicines, even those without a prescription.
Coumarin anticoagulants
Cefixime should be administered with caution in patients treated with coumarin anticoagulants, eg warfarin. Since cefixime may enhance the effects of anticoagulants, an increase in prothrombin time may occur with or without bleeding.
Other forms of interaction
The administration of cephalosporins can interfere with the results of some laboratory tests, causing false positivity of glycosuria with the Benedict, Fehling and "Clinitest" methods (but not with enzymatic methods). Positive Coombs test (sometimes false) have been reported during treatment with cephalosporins.
Warnings It is important to know that:
The indiscriminate use of antibiotics can cause the development of non-sensitive germs as well as the alteration of the germs that normally live in the intestine (colon flora). In very rare cases a selection of some germs (clostridia) can occur which, increasing by number, can cause a severe form of colitis called pseudomembranous. Mild cases of colitis usually regress spontaneously upon discontinuation of treatment, but if this does not happen, consult your doctor immediately. In such cases it is necessary to administer vancomycin orally which is the antibiotic of choice in case of pseudomembranous colitis.
Before starting treatment with SUPRAX, a thorough medical history should be taken in order to highlight any previous hypersensitivity reactions to cephalosporins, penicillins or other drugs.
SUPRAX should be used with caution in people allergic to penicillins. Partial cross-allergenicity between penicillin and cephalosporins has been ascertained both in vivo (in humans) and in vitro and, although rare, there have been reports of patients experiencing anaphylactic-type reactions, especially after parenteral administration.
Antibiotics should be administered with caution to all those patients who have previously experienced allergy phenomena, especially towards drugs. The onset of any allergic type reaction requires the suspension of treatment.
In the medium or severe forms, the treatment will be supplemented by the administration of electrolyte solutions and proteins.
The simultaneous use of drugs that reduce bowel motility must be absolutely avoided.
Serious skin adverse reactions such as toxic epidermal necrolysis, Stevens-Johnson syndrome, and skin erythema with eosinophilia and systemic symptoms (DRESS) have been reported in some patients receiving cefixime. When severe skin adverse reactions occur, it should be cefixime therapy discontinued and appropriate therapies and / or precautionary measures should be instituted.
With the use of SUPRAX, variations, however slight and reversible, in parameters related to hepatic, renal and blood crase function (thrombocytopenia, leukopenia and eosinophilia) have occasionally been detected.
In patients with severe renal insufficiency, on hemodialysis or peritoneal dialysis, the dosage of SUPRAX should be appropriately reduced (see section "Dose, method and time of administration").
Cases of haemolytic anemia, including severe cases with fatal outcome, have been reported following treatment with cephalosporin class drugs. Recurrent episodes of haemolytic anemia have also been reported following cephalosporin administration in patients who had previously developed amolytic anemia following first administration with cephalosporins (including cefixime).
Pregnancy and breastfeeding
Ask your doctor or pharmacist for advice before taking any medicine.
During pregnancy and breastfeeding, antibiotics, and in general all medicines, should be administered only in cases of real need, under the direct supervision of the doctor. In particular, although no toxic action on the embryo has been demonstrated and although cephalosporins are considered relatively safe even in pregnancy, it is better to avoid administration of SUPRAX, as a precaution, in the first three months of pregnancy. There is no data on the passage of SUPRAX into breast milk.
Effects on the ability to drive a vehicle or use machines.
Not relevant.
Suprax 400 mg dispersible tablets contain azo dyes (E110) which may cause allergic reactions
Dosage and method of use How to use Suprax: Dosage
The recommended doses are as follows:
Adults: 400 milligrams (mg), equivalent to 1 tablet of SUPRAX 400 mg coated tablets or SUPRAX 400 mg dispersible tablets, taken orally once daily. SUPRAX 400 mg coated tablet should be swallowed; SUPRAX 400 mg dispersible tablet can be dissolved in a little water (and then drunk) or swallowed as it is. Taking SUPRAX dispersible tablets after dissolving in water is particularly suitable for patients with swallowing difficulties.
Children: 0.4 milliliters (ml) of suspension for each kilo (kg) of body weight, equal to 8 mg / kg, once a day. A calibrated measuring cup and syringe are attached to the package of SUPRAX granules to allow the correct dosage of the drug both in older children (measuring cup) and in younger children (dosing syringe). The following scheme facilitates the calculation of the milliliters (ml) to be administered according to body weight.
SUPRAX can be administered either close to or between meals, indifferently.
It is advisable to take the drug at the set time in order to maintain constant concentrations in the body.
The safety of cefixime in children weighing less than 10 kg has not been established.
Instructions for opening the bottle
The bottle is equipped with a cap with a "child-proof" safety closure. To open the bottle, press the cap firmly and turn counterclockwise at the same time.
Instructions for preparing the suspension
To the granulate contained in the bottle, add water up to the level indicated by the arrow.
After adding the water, shake well until the granulate is completely dispersed.
Wait a few minutes.
If a level of suspension lower than that indicated by the arrow is highlighted, add more water to bring the level back to that indicated by the arrow.
Shake vigorously again.
The suspension thus prepared can be stored at room temperature for up to 14 days, during which it maintains its activity unchanged.
Shake vigorously before use.
There is no need to refrigerate.
Particular dosage regimens
In patients with severe renal insufficiency (creatinine clearance values <20 ml / min), on peritoneal dialysis or on hemodialysis, the recommended dosage is 200 mg once daily. In subjects with creatinine clearance> 20 ml / min, in the elderly and in subjects with hepatic insufficiency, no special dosage regimens are generally required.
Duration of treatment
All antibiotics should be used at full dosage for at least 5 days, before they are considered ineffective.
Based on experimental clinical data, 7 days of SUPRAX therapy may be sufficient to cure most infections. However, in severe cases, SUPRAX can also be used for 14 consecutive days.
Overdose What to do if you have taken an overdose of Suprax
Up to 2 grams per day (equal to 5 tablets of 400 mg or the whole bottle of granules), SUPRAX showed, in healthy volunteers, the same tolerability observed in patients treated with the recommended therapeutic doses. However, in case of ingestion / Accidental intake of an overdose of SUPRAX, notify your doctor immediately or go to the nearest hospital.
IF YOU ARE IN ANY DOUBT ABOUT THE USE OF THIS MEDICINAL PRODUCT, CONTACT YOUR DOCTOR OR PHARMACIST.
WHAT TO DO IF YOU HAVE FORGOTTEN TO TAKE ONE OR MORE DOSES
If the patient forgets the daily dose at the appointed time (for example in the evening) he should take it as soon as possible (for example the next morning: in this case, two doses will be taken on the same day).
Side Effects What are the side effects of Suprax
Like all medicines, this medicine can cause side effects, although not everybody gets them.
With cephalosporins these are essentially limited to gastrointestinal disorders and, occasionally, to hypersensitivity phenomena (allergic or other). The possibility of occurrence of the latter is greater in individuals who have previously experienced hypersensitivity reactions and in those with a history of allergy, hay fever, urticaria and allergic asthma.
The following reactions have been rarely reported during therapy with cefixime:
- Gastrointestinal: glossitis, nausea, vomiting, heartburn, abdominal pain, diarrhea and digestive difficulties. Switching to twice daily administration (200 mg twice a day) can remedy the problem of diarrhea. The onset of severe and prolonged diarrhea has been related to the use of different classes of antibiotics. In this case, the possibility of pseudomembranous colitis should be considered and it is advisable to consult the treating physician immediately.
- Allergic: Serum sickness-like reactions, anaphylaxis, joint pain (arthralgia) and drug fever.
- haematological: changes in some laboratory parameters: transient decrease in some types of white blood cells (granulocytopenia, in particular neutropenia) and platelets (thrombocytopenia), transient increase in another type of white blood cell (eosinophilia). There have been reports of haemolytic anemia following treatment with cephalosporins.
- Liverworts: jaundice, transient increase in ALT and AST transaminase levels, alkaline phosphatase and bilirubin.
- Renal : transient increase in BUN and serum creatinine concentrations.
- Respiratory: difficulty in breathing.
- Cutaneous: urticaria, skin rash, pruritus, erythema multiforme, Steven-Johnson syndrome, toxic epidermal necrolysis.
- Nervous system: headache, dizziness.
- General conditions: fever, face edema.
Other reactions reported were: anorexia, Candida vaginitis. Compliance with the information contained in this leaflet reduces the risk of undesirable effects.
Reporting of side effects
If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. Undesirable effects can also be reported directly through the national reporting system at the address https://www.aifa.gov.it/content/segnalazioni-reazioni-avverse
By reporting side effects you can help provide more information on the safety of this medicine.
Expiry and Retention
Expiry: see the expiry date indicated on the package.
The expiry date indicated refers to the product in intact packaging, correctly stored.
Warning: do not use the medicine after the expiry date shown on the package.
SUPRAX granules for oral suspension
Store at a temperature not exceeding 30 ° C.
The suspension after reconstitution must be stored at a temperature not exceeding 25 ° C.
Once reconstituted, the suspension must be used within 14 days.
Do not refrigerate.
SUPRAX 400 mg coated tablets
Store at a temperature not exceeding 30 ° C.
SUPRAX 400 mg dispersible tablets
Store at a temperature not exceeding 30 ° C.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. This will help protect the environment.
Keep this medicine out of the sight and reach of children.
COMPOSITION
SUPRAX 400 mg coated tablets
Each coated tablet contains:
Active ingredient: cefixime 400 mg.
Excipients: microcrystalline cellulose, pregelatinised starch, dibasic calcium phosphate dihydrate, magnesium stearate, hydroxypropylmethylcellulose, sodium laurilsulfate, titanium dioxide, liquid paraffin.
SUPRAX 100mg / 5ml granules for oral suspension
Each bottle of 100ml 2% contains:
Active ingredient: cefixime 2.0 g.
Excipients: sucrose, xanthan gum, sodium benzoate, strawberry flavor.
SUPRAX 400 mg dispersible tablets
Each dispersible tablet contains:
Active ingredient: cefixime 400 mg.
Excipients: microcrystalline cellulose, hydroxypropylcellulose, anhydrous colloidal silica, povidone, strawberry flavor FA 15757, strawberry flavor PV 4284, magnesium stearate, calcium saccharin, orange-yellow dye (E110).
PHARMACEUTICAL FORM AND CONTENT
Coated tablets: 5 tablets of 400 mg.
Granules for oral suspension 100mg / 5ml: bottle of 100ml.
Dispersible tablets: 5 and 7 tablets of 400 mg.
Source Package Leaflet: AIFA (Italian Medicines Agency). Content published in January 2016. The information present may not be up-to-date.
To have access to the most up-to-date version, it is advisable to access the AIFA (Italian Medicines Agency) website. Disclaimer and useful information.
01.0 NAME OF THE MEDICINAL PRODUCT
SUPRAX
02.0 QUALITATIVE AND QUANTITATIVE COMPOSITION
SUPRAX 400 mg coated tablets
One 400 mg coated tablet contains:
Active ingredient: cefixime 400 mg
SUPRAX 100 mg / 5ml granules for oral suspension
One bottle of 2% granules for oral suspension of 100 ml contains:
Active ingredient: cefixime 2 g
SUPRAX 400 mg dispersible tablets
Each 400 mg dispersible tablet contains:
Active ingredient: cefixime 400 mg
03.0 PHARMACEUTICAL FORM
Coated tablets
Granules for oral suspension
Dispersible tablets
04.0 CLINICAL INFORMATION
04.1 Therapeutic indications
SUPRAX is indicated in the treatment of infections caused by microorganisms sensitive to cefixime and in particular:
- upper respiratory tract infections (pharyngitis, tonsillitis);
- ENT infections (otitis media, etc.);
- lower respiratory tract infections (pneumonia, bronchitis);
- kidney and urinary tract infections.
04.2 Posology and method of administration
In adults, the recommended posology is once daily administration (one tablet per day of SUPRAX 400 mg coated tablets or SUPRAX 400 mg dispersible tablets). SUPRAX 400 mg coated tablet should be swallowed; SUPRAX 400 mg dispersible tablet can be dissolved in a little water (and then drunk) or swallowed as it is. The intake of SUPRAX dispersible after dissolution in water is particularly suitable for patients with functional or organic swallowing difficulties.
In children, the recommended dose of cefixime suspension at 2% is 8 mg / kg / day in a single administration, i.e. according to weight (see diagram below):
SUPRAX can be taken indifferently both close to and between meals.
Based on experimental clinical data, 7 days of SUPRAX therapy may be sufficient to cure most infections. However, in severe cases SUPRAX can also be used for 14 days.
A calibrated measuring cup and syringe are attached to the package of SUPRAX 100 mg / 5ml granules that allow a precise dosage of the drug in both older and younger children.
Instructions for preparing the suspension
Add water to the granules contained in the bottle up to the point indicated by the arrow.
After adding water, shake well until the powder is completely dispersed.
Wait a few minutes; if the suspension level is lower than that indicated by the arrow, add more water to bring the level back to that indicated by the arrow.
Shake vigorously again.
The suspension thus prepared can be stored up to 14 days during which it keeps its activity unchanged.
Shake the bottle containing the suspension well before use.
Particular dosage regimens
In patients with creatinine clearance values on outpatient or hemodialysis peritoneal dialysis, the recommended dosage is 200 mg once daily. In general, no special dosing regimens are required in subjects with creatinine clearance> 20 ml / min, in the elderly and in subjects with hepatic insufficiency.
04.3 Contraindications
Hypersensitivity to the active substance or to any of the excipients.
The medicinal product is also generally contraindicated in subjects with hypersensitivity to penicillins and cephalosporins (see section 4.4).
04.4 Special warnings and appropriate precautions for use
Before starting treatment with SUPRAX, a thorough medical history should be taken in order to highlight any previous hypersensitivity reactions to cephalosporins, penicillins or other drugs.
SUPRAX should be used with caution in people allergic to penicillins. Partial cross-allergenicity between penicillin and cephalosporins has been ascertained both in vivo (in humans) and in vitro and, although rare, there have been reports of patients experiencing anaphylactic-type reactions, especially after parenteral administration.
Antibiotics should be administered with caution to all those patients who have previously experienced allergy phenomena, especially towards drugs. The onset of any allergic type reaction requires the suspension of treatment.
Prolonged use of antibiotics can cause the development of non-sensitive germs and in particular an alteration of the normal flora of the colon with possible selection of clostridia responsible for pseudomembranous colitis. Mild cases of pseudomembranous colitis can regress with the interruption of treatment. If the colitis does not regress with the adoption of these measures, vancomycin should be administered orally which is the antibiotic of choice in case of pseudomembranous colitis.
In the medium or severe forms, the treatment will be supplemented by the administration of electrolyte solutions and proteins.
The simultaneous use of drugs that reduce peristalsis must be absolutely avoided.
Broad spectrum antibiotics should be administered with caution in patients with a history of gastrointestinal disease, particularly colitis.
With the use of SUPRAX, slight and reversible changes in parameters related to hepatic, renal and blood counts (thrombocytopenia, leukopenia, and eosinophilia) have occasionally been observed. In patients with severe renal insufficiency, on hemodialysis or on dialysis peritoneal the dosage of SUPRAX should be appropriately reduced (see section 4.2).
Do not leave medicines within the reach of children.
04.5 Interactions with other medicinal products and other forms of interaction
The administration of cephalosporins can interfere with the results of some laboratory tests, causing false positivity of glycosuria with the Benedict, Fehling and "Clinitest" methods (but not with the enzymatic methods). Positive Coombs test (sometimes false) have been reported during treatment with cephalosporins.
04.6 Pregnancy and lactation
In pregnant and breastfeeding women, the product should be administered in cases of real need, under direct medical supervision.
In particular, although no embryotoxic action has been demonstrated, the administration of SUPRAX should be avoided, as a precaution, in the first three months of pregnancy.
There is no data on the passage of the drug into breast milk.
04.7 Effects on ability to drive and use machines
The substance does not affect the ability to drive and use machines.
04.8 Undesirable effects
With cephalosporins, undesirable reactions are essentially limited to gastrointestinal disturbances and, occasionally, to hypersensitivity phenomena.
The possibility of occurrence of the latter is greater in individuals who have previously experienced hypersensitivity reactions and in those with a previous history of allergy, hay fever, urticaria and allergic asthma.
The following reactions have been rarely reported during therapy with cefixime:
- Gastrointestinal: glossitis, nausea, vomiting, heartburn, abdominal pain and diarrhea. Switching to twice daily administration (200 mg twice a day) can remedy the problem of diarrhea. The occurrence of severe and prolonged diarrhea has been related to the use of different classes of antibiotics. In this case, the possibility of pseudomembranous colitis must be considered. In the event that the colonoscopic examination confirms the diagnosis, the antibiotic in use should be discontinued immediately and oral vancomycin treatment initiated.Peristalsis inhibitor drugs are contraindicated.
- Allergic: anaphylaxis, mild hives or skin rash, itching, arthralgia, and drug fever.
- Hematological: changes in some laboratory parameters: transient neutropenia, granulocytopenia, thrombocytopenia and eosinophilia. There have been reports of haemolytic anemia following treatment with cephalosporins.
- Liverworts: transient increase in serum transaminases (ALT, AST), alkaline phosphatase and total bilirubin.
- Renal: transient increase in urea nitrogen and serum creatinine concentrations.
- Other reactions reported were: anorexia, headache, dizziness, Candida vaginitis.
04.9 Overdose
Up to 2 grams per day, in healthy volunteers, the drug exhibited the same tolerability profile observed in patients treated with recommended therapeutic dosages.
However, in the event of an overdose, it would be advisable to consider the possibility of a gastric lavage.
Cefixime is not eliminated from the circulation in significant quantities by dialysis.
05.0 PHARMACOLOGICAL PROPERTIES
05.1 Pharmacodynamic properties
Pharmacotherapeutic group: antibacterial for systemic use, belonging to the class of cephalosporins. ATC: J01DD08
Mechanism of action:
SUPRAX is a new cephalosporin for oral use characterized by a broad spectrum bactericidal activity and by a high resistance to the hydrolytic activity of beta-lactamases.
The bactericidal activity of cefixime is due to the inhibition of the synthesis of the bacterial cell wall. It is active in vitro against a "wide range of clinically significant Gram-positive and Gram-negative pathogens. Cefixime is particularly active against the following genera: Streptococcus (excluding enterococci), Haemophilus, Branhamella, Neisseria, Escherichia , Klebsiella, Proteus, Enterobacter, Pasteurella, Providencia, Salmonella, Shigella, Citrobacter, Serratia, but are mostly resistant to cefixime: Pseudomonas sp., Staphilococcus sp., Listeria monocytogenes, Bacteroides fragilis and Clostridium sp.
05.2 "Pharmacokinetic properties
After a single oral administration of 200 mg the maximum concentration of cefixime in serum is 3 mcg / ml and this level is achieved within 3 to 4 hours.
After a single oral administration of 400 mg the maximum serum concentration is higher (3.5 to 4 mcg / ml), even if there is no direct proportionality with the dose taken.
After the repeated administration of 400 mg / day orally (one or two administrations per day) for 15 days, the serum levels and bioavailability are not modified, which testifies to the absence of accumulation of the drug in the organism.
After the administration of 8 mg / kg of cefixime in suspension, in pediatric patients, serum concentrations similar to those reached in adults after a dose of 400 mg are obtained.
The absolute bioavailability of cefixime is approximately 50% and is not affected by food. In this case, the time required to reach the peak concentration is delayed by approximately 1 hour.
The apparent volume of distribution is 17 liters.
In animals, the distribution of cefixime in most tissues (excluding the brain) results in higher tissue concentrations than the M.I.C. of susceptible strains (0.20 mcg / ml).
The elimination kinetics of cefixime are characterized by a half-life of between 3 and 4 hours.
The drug is eliminated unchanged by the kidney (16 to 25%). Extra-renal elimination occurs mainly via the biliary route. No serum or urinary metabolites have been detected in humans or animals.
Pharmacokinetic parameters are slightly modified in the elderly population. The slight increase in serum concentrations, bioavailability and quantity of the drug excreted (from 15 to 25%) do not require modifications of the daily dose in this particular population.
In severe renal insufficiency (plasma creatinine clearance, half-life and peak serum concentrations require a dose reduction from 400 to 200 mg / day.
In case of hepatic insufficiency, elimination is slowed (t½ = 6.4 h), but it is not necessary to change the daily dose.
Protein binding is approximately 70%, mainly with albumin and independent of concentration (at therapeutic dose levels).
05.3 Preclinical safety data
After oral administration the LD5050 values were higher than 10 g / kg in mice, rats and rabbits. After iv, ip, sc administration, the LD5050 values were higher than 3, 7 and 10 g / kg in the mouse and 5, 8, 10 g / kg in the rat, respectively.
Cefixime was found to be devoid of teratogenic effects and did not affect fertility in the animals tested.
06.0 PHARMACEUTICAL INFORMATION
06.1 Excipients
SUPRAX 400 mg coated tablets
One coated tablet contains:
microcrystalline cellulose, pregelatinised starch, dibasic calcium phosphate dihydrate, magnesium stearate.
Coating: hydroxypropylmethylcellulose, sodium lauryl sulfate, titanium dioxide (E171), liquid paraffin.
SUPRAX 100 mg / 5ml granules for oral suspension
One bottle of 2% granules for oral suspension of 100 ml contains:
sucrose, xanthan gum, sodium benzoate, strawberry flavor.
SUPRAX 400 mg dispersible tablets
One breakable tablet contains:
microcrystalline cellulose, hydroxypropylcellulose, anhydrous colloidal silica, povidone, strawberry flavor FA 15757, strawberry flavor PV 4284, magnesium stearate, calcium saccharin, orange-yellow dye (E110)
06.2 Incompatibility
None.
06.3 Period of validity
SUPRAX 400 mg coated tablets
36 months in intact packaging.
SUPRAX 100 mg / 5ml granules for oral suspension
24 months in intact packaging.
SUPRAX 400 mg dispersible tablets
24 months in intact packaging.
06.4 Special precautions for storage
SUPRAX 100 mg / 5ml granules for oral suspension:
None with intact packaging.
The suspension after reconstitution must be stored at a temperature not exceeding 30 ° C.
Once reconstituted, the suspension must be used within 14 days.
Do not refrigerate.
SUPRAX 400 mg coated tablets:
Store at a temperature not exceeding 30 ° C.
SUPRAX 400 mg dispersible tablets:
Store at a temperature not exceeding 30 ° C.
06.5 Nature of the immediate packaging and contents of the package
SUPRAX 400 mg coated tablets;
5 tablets of 400 mg in aluminum-PVDC-PVC blisters;
SUPRAX 100 mg / 5ml granules for oral suspension
100 ml (100 mg / 5 ml) in amber glass bottle + Measuring cup + Syringe-measuring device.
SUPRAX 400 mg dispersible tablets:
7 divisible tablets of 400 mg in aluminum-PVDC-PVC blisters;
SUPRAX 400 mg dispersible tablets:
5 divisible tablets of 400 mg in aluminum-PVDC-PVC blisters;
06.6 Instructions for use and handling
See point 4.2
07.0 MARKETING AUTHORIZATION HOLDER
Astellas Pharma S.p.A.
Via delle Industrie, 1
20061 Carugate (Milan)
08.0 MARKETING AUTHORIZATION NUMBER
027127036 - SUPRAX 400 mg coated tablets - 5 Tablets
027127101 - SUPRAX 100 mg / 5ml granules for oral suspension
027127087 - SUPRAX 400 mg dispersible tablets - 5 Tablets
027127075 - SUPRAX 400 mg dispersible tablets - 7 Tablets
09.0 DATE OF FIRST AUTHORIZATION OR RENEWAL OF THE AUTHORIZATION
May 1995 / June 2010
10.0 DATE OF REVISION OF THE TEXT
09/2010
