Nilicon

Ceftriaxone Sodium
Antibiotic

Nilicon

Nilicon is a 3rd generation broad-spectrum parenteral cephalosporin antibiotic. It has potent bactericidal activity against a wide range of Gram-positive and Gram-negative organisms. Nilicon like other cephalosporins and penicillins kills bacteria by interfering with the synthesis of the bacterial cell wall. Nilicon has a high degree of stability in the presence of beta lactamases.

Description

Composition:

Nilicon 250 mg IM/IV Injection: Each vial contains dry powder equivalent to 250 mg Ceftriaxone (as sterile Ceftriaxone Sodium USP) and 1 ampoule of 2 ml 1% Lidocaine Injection USP for IM injection or 5 ml Water for Injection BP for IV injection.

Nilicon 500 mg IM/IV Injection: Each vial contains dry powder equivalent to 500 mg Ceftriaxone (as sterile Ceftriaxone Sodium USP) and 1 ampoule of 2 ml 1% Lidocaine Injection USP for IM injection or 5 ml Water for Injection BP for IV injection.

Nilicon 1 g IM/IV Injection: Each vial contains dry powder equivalent to 1 g Ceftriaxone (as sterile Ceftriaxone Sodium USP) and 1 ampoule of 3.5 ml Lidocaine 1% Injection USP for IM injection or 10 ml Water for Injection BP for IV injection.

Nilicon 2 g IV Injection: Each vial contains dry powder equivalent to 2 g Ceftriaxone ( as sterile Ceftriaxone Sodium USP) and 2 ampoules of 10 ml Water for Injection BP for IV injection.

Pharmacology:

Nilicon is a 3rd generation broad-spectrum parenteral cephalosporin antibiotic. It has potent bactericidal activity against a wide range of Gram-positive and Gram-negative organisms. Nilicon like other cephalosporins and penicillins kills bacteria by interfering with the synthesis of the bacterial cell wall. Nilicon has a high degree of stability in the presence of beta lactamases. A remarkable feature of Nilicon is its relatively long plasma elimination half-life of about 6 to 9 hours, which makes single or once-daily dosage of the drug appropriate for most patients. Ceftriaxone is not metabolized in the body. About 40-65% of a dose of Ceftriaxone is excreted unchanged in the urine; the remainder is excreted in the bile and ultimately found in the feces as unchanged drug and microbiologically inactive compound. The drug is highly protein bound (95%).

Indications:

Nilicon is indicated for the treatment of the following major infections:
1. Renal and urinary tract infections
2. Lower respiratory tract infections, particularly pneumonia
3. Gonococcal infections
4. Skin,soft tissue, bone and joint infections
5. Bacterial meningitis
6. Serious bacterial infections e.g. septicemia
7. ENT infections
8. Infections in cancer patients
9. Prevention of postoperative infections
10. Perioperative prophylaxis of infections associated with surgery
11. Typhoid fever.

 

Dosage & Administration:

Adult: By deep intramuscular injection, or by intravenous injection over at least 2-4 minutes, or by intravenous infusion, 1 g daily; 2-4 g daily in severe infections; intramuscular doses over 1 g divided between more than one site. Neonate: By intravenous infusion over 60 minutes, 20-50 mg/kg daily (max.50 mg/kg daily). Infant and child under 50 kg: by deep intramuscular injection or by intravenous injection over 2-4 minutes or by intravenous infusion, 20-50 mg/kg daily; up to 80 mg/kg daily in severe infections; doses of 50 mg/kg and over by intravenous infusion only; 50 kg and over, adult dose.
Uncomplicated gonorrhea: by deep intramuscular injection, 250 mg as a single dose. Surgical prophylaxis: by deep intramuscular injection or by intravenous injection over at least 2-4 minutes, 1 g at induction, Colorectal surgery: by deep intramuscular injection or by intravenous injection over at least 2-4 minutes or by intravenous infusion, 2 g at induction; intramuscular doses over 1 g divided between more than one site.

Duration of therapy: Continue for more than 2 days after signs and symptoms of infection have disappeared. Usual duration is 4 to 14 days; in complicated infections, longer therapy may be required.

Preparation of Solutions for Intramuscular/intravenous Injections:
For intramuscular injection: 250 mg or 500 mg Nilicon should be dissolved in 2 ml of 1% Lidocaine Injection USP or 1 g Nilicon in 3.5 ml of 1% Lidocaine Injection USP. For intravenous injection: 250 mg or 500 mg Nilicon should be dissolved in 5 ml of Water for Injection BP or 1 g Nilicon in 10 ml of Water for Injection BP or 2 g Nilicon in 20 ml of Water for Injection BP. The injection should be administered over 2-4 minutes, directly into the vein or via the tubing of an intravenous infusion. The use of freshly reconstituted solution is recommended. However, it maintains potency for at least 6 hours at room temperature or 24 hours at 5°C.

 

Contraindication:

Ceftriaxone should not be given to patients with a history of hypersensitivity to cephalosporin antibiotics.

Warning & Precaution:

The admixture of beta-lactam antibacterials (penicillins and cephalosporins) and aminoglycosides may result in substantial mutual inactivation. If they are administered concurrently , they should be administered in separate sites. Do not mix them in the same intravenous bag or bottle.

Side Effects:

Ceftriaxone is generally well tolerated. A few side effects such as gastro-intestinal effects including diarrhoea, nausea and vomiting, stomatitis & glossitis; cutaneous reactions including rash, pruritus, urticaria, oedema & erythema multiforme; hematologic reactions including eosinophilia, thrombocytopenia, leucopenia, anemia and neutropenia; hepatic reactions including elevations of SGOT or SGPT, bilirubinemia; CNS reactions including headache, hyperactivity, nervousness, sleep disturbances, confusion, hypertonia and dizziness were reported. Local phlebitis occurs rarely following intravenous administration but can be minimized by slow injections over 2-4 minutes.

Drug interaction:

No drug interactions have been observed with diuretics or with aminoglycosides.

 

Packing:

Nilicon 250 mg IM Injection: Combipack of 1 vial containing 250 mg Ceftriaxone (as sterile Ceftriaxone Sodium USP) and 1 ampoule of 2 ml 1% Lidocaine Injection USP.
Nilicon 250 mg IV Injection: Combipack of 1 vial containing 250 mg Ceftriaxone (as sterile Ceftriaxone Sodium USP) and 1 ampoule of 5 ml Water for Injection BP.
Nilicon 500 mg IM Injection: Combipack of 1 vial containing 500 mg Ceftriaxone (as sterile Ceftriaxone Sodium USP) and 1 ampoule of 2 ml 1% Lidocaine Injection USP.
Nilicon 500 mg IV Injection: Combipack of 1 vial containing 500 mg Ceftriaxone (as sterile Ceftriaxone Sodium USP) and 1 ampoule of 5 ml Water for Injection BP.
Nilicon 1g IM Injection: Combipack of 1 vial containing 1g Ceftriaxone (as sterile Ceftriaxone Sodium USP) and 1 ampoule of 3.5 ml 1% Lidocaine Injection USP.
Nilicon 1g IV Injection: Combipack of 1 vial containing 1g Ceftriaxone (as sterile Ceftriaxone Sodium USP) and 1 ampoule of 10 ml Water for Injection BP.
Nilicon 2g IV Injection: Combipack of 1 vial containing 2 g Ceftriaxone (as sterile Ceftriaxone Sodium USP) and 2 ampoules of 10 ml Water for Injection BP.