INDICATIONS     CONTRA-INDICATIONS     DOSAGE     SIDE-EFFECTS     PREGNANCY     OVERDOSE     IDENTIFICATION     PATIENT INFORMATION
DACEF SUSPENSION 250 mg/5 mL
DACEF SUSPENSION 500 mg/5 mL
DACEF CAPSULES 500 mg

SCHEDULING STATUS:
S4

PROPRIETARY NAME
(and dosage form):

DACEF SUSPENSION 250 mg/5 mL
DACEF SUSPENSION 500 mg/5 mL
DACEF CAPSULES 500 mg

COMPOSITION:
POWDERS OF ORAL SUSPENSION :
Powders providing cefadroxil monohydrate equivalent to 250 mg and 500 mg cefadroxil per 5 mL respectively when reconstituted, containing approximately 0,1% m/v sodium benzoate as preservative.

CAPSULES:
Capsules containing cefadroxil monohydrate equivalent to and 500 mg cefadroxil.

PHARMACOLOGICAL CLASSIFICATION:
A20.1.1 Broad spectrum antibiotic.

PHARMACOLOGICAL ACTION:
CLINICAL PHARMACOLOGY:
DACEF (cefadroxil monohydrate) is a semisynthetic antibiotic with a broad spectrum of bactericidal activity. It is chemically designated as 7[[D-2-amino-2(4-hydroxyphenyl) acetyl] amino]-3-methyl-8-oxo-5-tia-1-azabicyclo [4.2.0]oct-2-ene-2-carboxylic acid monohydrate.
DACEF is stable in the presence of acid and is rapidly absorbed after oral administration.
Following single oral doses of 250, 500 and 1 000 mg, average peak serum concentrations are approximately 9, 16 and 28 µg/mL respectively. Measurable levels are present 12 hours after administration. DACEF is approximately 20% bound to serum proteins. DACEF has been shown to be widely distributed in most body tissues, including tonsils, bronchial secretions, pleural fluid, liver and bile and prostate. Approximately 80% of the medicine is excreted unchanged in the urine within eight hours. Peak urine concentrations reach approximately 1 800 µg/mL following a single 500 mg dose.
Urine DACEF concentration was maintained well above minimum inhibitory concentration of susceptible urinary pathogens for 20 to 22 hours following a single one gram dose.
Increases in dosage generally produce a proportional increase in DACEF serum and urinary concentrations.

MICROBIOLOGY:
DACEF is bactericidal in vitro against a wide range of Gram-positive and Gram-negative micro-organisms. Sensitive Gram-positive organisms include penicillinase and-non-penicillinase producing staphylococci, ß-haemolytic streptococci, Streptococcus pneumoniae and Streptococcus pyogenes. Strains of sensitive Gram-negative organisms include Escherichia coli, Klebsiella pneumoniae and some strains of Proteus mirabilis, Haemophilus influenzae and Shigella spp. In vitro sensitivity does not necessarily imply in vivo efficacy.

NOTE:
MOST STRAINS OF ENTEROCOCCI (STREP. FAECALIS AND S. FAECIUM) ARE RESISTANT TO DACEF. DACEF HAS NO ACTIVITY AGAINST PSEUDOMONAS SPECIES AND ACINETOBACTER CALCOACETICUS (FORMERLY MIMA AND HERELLEA SPECIES).

DISC SUSCEPTIBILITY TESTS:
The most practical applicable estimate of antibiotic sensitivity is the measurement of zone diameters on disc testing. Interpretations correlate zone diameters of disc test with minimum inhibitory concentration values for DACEF. With this procedure, a report of “resistant”from the laboratory indicates that the infecting organism is not likely to respond to therapy. A report of “intermediate susceptibility” suggests that the organism would be susceptible if the infection is confined to the urinary tract, as DACEF produces high antibiotic levels in the urine.

INDICATIONS:
DACEF is indicated in the treatment of the following infections when due to susceptible microorganisms:
Respiratory tract infections, urinary tract infections and skin and soft tissue infections.

CONTRA-INDICATIONS:
DACEF is contra-indicated in patients with known allergy to the cephalosporin group of antibiotics. The safe use of DACEF during pregnancy has not been established. Safety in premature infants and neonates has not been established.

WARNINGS :
IN PENICILLIN-SENSITIVE PATIENTS, CEPHALOSPORIN ANTIBIOTICS SHOULD BE USED WITH GREAT CAUTION. THERE IS CLINICAL AND LABORATORY EVIDENCE OF PARTIAL CROSS-SENSITIVITY OF THE PENICILLINS AND CEPHALOSPORINS AND THERE ARE INSTANCES OF PATIENTS WHO HAVE HAD REACTIONS TO BOTH DRUGS (INCLUDING FATAL ANAPHYLAXIS AFTER PARENTAL USE).
Any patient who has demonstrated a history of some form of allergy, particularly to medicines should receive DACEF cautiously and then only when absolutely necessary.
Pseudomembranous colitis has been reported. Therefore it is important to consider its diagnosis in patients who develop diarrhoea in association with the use of DACEF.

DOSAGE AND DIRECTIONS FOR USE:
DACEF administered orally is well absorbed. Administration of the antibiotic may be made without regard to food as meals have no significant effect on absorption. Administration with food may be helpful in diminishing gastro-intestinal complaints occasionally associated with oral DACEF therapy.

Adults and children having a mass of more than 40 kg :
Urinary Tract Infections:
For accurate uncomplicated lower urinary tract infections (e.g. cystitis), the usual daily dosage is 1 or 2 grams per day in a single dose. In complicated or chronic urinary tract infections, the usual dosage is 1 g every 12 hours for a minimum of 7 - 10 days.

Skin and Skin Structure Infections:
For skin and skin structure infections the usual dosage is 1 gram per day in a single dose.

Upper Respiratory Tract Infections:
In upper respiratory infections the usual dosage is 500 mg every 12 hours. For Group A ß-haemolytic streptococcal pharyngitis and tonsillitis, 1 g DACEF may be given as a single, daily dose. For any infections caused by Group A ß-haemolytic streptococcus, treatment should be administered for 10 days.

Lower Respiratory Tract Infections:
For lower respiratory tract infections the recommended dosage is 500 mg to 1 g every 12 hours.

Children having a mass of less than 40 kg :
The following dosage chart is a useful guide* to DACEF therapy in children:

% of Adult Dose	Age and Mass	Total Daily Dosage (Based on range of 1 - 2 g for Adults)
75%	12 years (40 kg)	750 mg to 1,5 g
50%	7 years (23 kg)	500 mg to 1,0 g
25%	1 year (10 kg)	250 mg to 500 mg
12,5%	Full Term (3,2 kg)	125 mg to 250 mg

* using the Percentage Method based on formula :

Surface area of Child	x 100 = Percentage of Adult dose
Surface area of Adult

Urinary Tract Infections:
In acute uncomplicated urinary tract infections (e.g. cystitis) the recommended daily dose for children is 12,5 mg to 25 mg/kg every 12 hours. In complicated or chronic urinary tract infections the recommended dose for children is 25 mg/kg every 12 hours administered for 7- 10 days.

Skin and Skin Structure Infections:
For skin and skin structure infections the recommended dose for children is 25 mg/kg given once daily or 25 mg/kg every 12 hours depending of the sensitivity of the organism.

Upper and Lower Respiratory Tract Infections:
In respiratory tract infections the recommended dose for children is 25 mg/kg every 12 hours. For Group A ß-haemolytic streptococcal pharyngitis and tonsillitis, DACEF may be given as a single daily dose at 30 mg/kg/day. In infections caused by the Group A ß-haemolytic streptococcus, treatment should be administered for 10 days.

Dosage in Renal Impairment:
A modified dosage schedule is unnecessary in patients with creatinine clearance rates of greater than 50 mL/min. In those patients with creatinine clearance rates of 50 mL/min. or less, the following reduced dosage schedule is recommended as a guideline, based on the creatinine clearance rate (mL/min/1,73 m²). Each patient should be considered individually.
Patients with renal insufficiency may be treated with an initial dose equal to that chosen for a patient with normal renal function (see above). Subsequent doses may be administered according to the following table:

Creatinine clearance	Dose	Dose Interval
0-10 mL/min/1,73 m²	500 mg	36 hours
10-25 mL/min/1,73 m²	500 mg	24 hours
25-50 mL/min/1,73 m²	500 mg	12 hours

Further modifications of the dosage schedule may be necessary in children. Treatment should be continued for a minimum of 48 to 72 hours beyond the time that the patient becomes asymptomatic or evidence of bacterial eradication has been obtained. A MINIMUM OF 10 DAYS TREATMENT IS RECOMMENDED FOR ANY INFECTION CAUSED BY GROUP A BETA-HAEMOLYTIC STREPTOCOCCI. Chronic urinary tract infections may require prolonged intensive therapy with continued bacteriologic and clinical follow-up.

SIDE EFFECTS AND SPECIAL PRECAUTIONS:
DACEF may have the potential for producing allergic reactions. Rash, pruritus, urticaria and angioedema may be observed infrequently. Should an allergic reation to DACEF occur, the medicine should be discontinued and the patient treated with adrenaline, corticosteroids and/or antihistamines. CAUTION SHOULD BE EXERCISED WHEN DACEF IS ADMINISTERED TO A NURSING MOTHER.
Side-effects including nausea, vomiting, diarrhoea, dyspepsia and abdominal discomfort, dizziness, headache and monilial vaginitis may also occur. Reversible neutropenia, leukopenia and minor elevations in serum transaminase may occur. A false-positive Coombs' reaction may occur in some patients receiving DACEF therapy. Patients treated with DACEF may have a false-positive glycosuria reaction with Benedict's or Fehling's solutions, copper sulphate or Clinitest tablets are used in testing. This does not occur with enzyme-based tests such as Clinistix. Use of DACEF may result in the overgrowth of nonsusceptible organisms. If superinfection occurs during therapy, appropriate measures should be taken.

KNOWN SYMPTOMS OF OVERDOSAGE AND PARTICULARS OF ITS TREATMENT:
See "side-effects and special precautions". Treatment is symptomatic and supportive.

IDENTIFICATION:
POWDER FOR ORAL SUSPENSION:
Off-white powder. Reconstitution with water as per label directions produces an off-white, fruit-flavoured suspension.

CAPSULES:
Hard gelatine capsules comprising opaque, white caps and bodies printed with mortar and pestle and "LENNON" on one side and "DACEF 500" on the other side.

PRESENTATION.
POWDERS FOR ORAL SUSPENSION:
Powders in plastic bottles providing 60 mL of each strength when reconstituted.

CAPSULES:
Blister packs with 10 capsules.

STORAGE INSTRUCTIONS:
Store in a cool, dry place. Temperatures should not exceed 25°C.
NOTE:
Powders for oral suspension: The potency of reconstituted suspensions will be maintained for one week at room temperatures that do not exceed 25°C and for two weeks under refrigeration (2-8°C).
Keep out of reach of children.

REGISTRATION NUMBERS:

Suspensions:	250 mg/5 mL:	27/20.1.1/0433
	500 mg/5 mL:	27/20.1.1/0434
Capsules:	27/20.1.1/432

NAME AND BUSINESS ADDRESS OF APPLICANT:
Lennon Limited
7 Fairclough Road
Korsten
Port Elizabeth
6020

DATE OF PUBLICATION OF THIS PACKAGE INSERT:
December 1992

G179                065002
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