Composition

• Each Film Coated Tablet Contains:
• Cefixime Trihydrate IP
  200 mg
• Ofloxacin IP
  200 mg

Packing

• 10x10
  (Alu Alu)

MRP

• 110.60

Overview

Cefixime Trihydrate is an oral third generation cephalosporin antibiotic used to treat infections caused by bacteria such as pneumonia; bronchitis; gonorrhea; and ear, lung, throat, and urinary tract infections.Cefixime is used to treat many different types of infections caused by bacteria. Cefixime may also be used for other purposes not listed in this medication guide.
Ofloxacin is a synthetic chemotherapeutic antibiotic of the fluoroquinolone drug class considered to be a second-generation fluoroquinolone.

Indications

• Typhoid Fever
• Urinary Tract Infection
• Respiratory Tract Infection
• Nosocomial Infections
• Soft Tissue Infections
• Surgical Prophylaxis
• Intra-abdominal Infections.

Rationale of Combination

• Unique Dual Mode Of Action
• Ofloxacin-Prevents nucleic acid synthesis
• Cefixime-Inhibits cell wall synthesis
• Acts synergetically
• Gives better patient compliance.

Contraindications

This tablet is contraindicated In patients with known hypersensitivity to the cephalosporin or penicillin or fluoroquinolone antibiotics.

Pharmacology

Cefixime Trihydrate:
Absorption: About 40% to 50% is absorbed. C_max following 200 and 400 mg doses of oral suspension are 3 and 4.6 mcg/mL, respectively. Tmax occurs between 2 and 6 h following administration of 400 mg and between 2 and 5 h after a 200 mg dose.
Distribution: Protein binding is about 65%.
Elimination: About 50% of absorbed dose is excreted unchanged in the urine in 24 h. Serum t 1/2 averages 3 to 4 h, but may be as long as 9 h in some healthy subjects.

Ofloxacin:
Absorption: Following oral administration, the bioavailability of ofloxacin in the tablet formulation is approximately 98%. Maximum serum concentrations are achieved one to two hours after an oral dose.
Half life: 9 hours.
Elimination: Elimination is mainly by renal excretion. Between 65% and 80% of an administered oral dose of ofloxacin is excreted unchanged via the kidneys within 48 hours of dosing. Four to eight percent of an ofloxacin dose is excreted in the feces. This indicates a small degree of biliary excretion of ofloxacin.

Mechanism of Action

This tablet is one of the combination of cefixime (cephalosporin) and ofloxacin (fluoroquinolone) and has unique dual mode of action i.e in this combination ofloxacin prevents nucleic acid synthesis of bacteria and cefixime inhibits bacterial cell wall synthesis.It is useful for killing thr ESBL (Extended Spectrum Beta-lactamase) bacteria.Both works instantly and synergistically and gives better patient compliance. Cefixime is an antibiotic, is a third generation cephalosporin like ceftriaxone and Cefotaxime.Cefixime is highly stable in the presence of beta lactamases enzymes.Cefixime is an effective treatment to stop the spread of several bacterial infections. It is often used as a treatment for gonorrhea, pharyngitis, typhoid fever and tonsillitis.ofloxacin belongs to fluoroquinolones group of antimicrobials i.e.-These are the quinolones having one or more fluorine substitution in their structure.Ofloxacin used to treat pneumonia and bronchitis caused by H.influenzae and S.pneumoniae.It is also used in treating skin infections caused by staphylococcus aureus and streptococcus pyogenes bacteria.

Interactions

Elevated carbamazepine levels have been reported when tablet is administrated concomitantly with carbamazepine salt and with warfarin and anticoagulants drugs, the prothrombin time is increased when this tablet is administrated concomitantly. Ofloxacin from chelates with alkaline earth and transition metal cations when administrated with antacids containing calcium, magnesium or aluminium, with sucralphate, with divalent or trivalent cations such as iron, or with multivitamins containing zinc. Elevated serum levels of cyclosporine have been reported with concomitant use of cyclosporine with some other quinolones.