Our Products
Composition
Triforce 500 mg IM Injection: Each vial contains sterile Ceftriaxone Sodium USP equivalent to 500 mg Ceftriaxone.
Triforce 1 g IM Injection: Each vial contains sterile Ceftriaxone Sodium USP equivalent to 1 g Ceftriaxone.
Triforce 1 g IV Injection: Each vial contains sterile Ceftriaxone Sodium USP equivalent to 1 g Ceftriaxone.
Triforce 2 g IV Injection: Each vial contains sterile Ceftriaxone Sodium USP equivalent to 2 g Ceftriaxone.
Pharmacology
Ceftriaxone 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. Like other cephalosporins and penicillins, Ceftriaxone kills bacteria by interfering with the synthesis of the bacterial cell wall. Ceftriaxone has a high degree of stability in the presence of beta lactamases. A remarkable feature of Ceftriaxone 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%).
Indication
• Ceftriaxone is indicated for the treatment of the following major infections:
• Lower respiratory tract infections
• Acute Bacterial Otitis Media
• Skin and skin structure infections
• Urinary tract infections
• Gonorrhea
• Bacterial Septicemia
• Bone and joint infections
• Meningitis
• Prevention of postoperative infections
• Perioperative prophylaxis of infections associated with surgery
Dose & administration
Adult: The usual dose is 1 to 2 g by intravenous or intramuscular administration once a day (or in equally divided doses twice a day).
Pneumonia, Bronchitis, Acute bacterial otitis media, Skin and skin structure infection, Urinary tract infections, Bacterial Septicemia, Bone and joint infections, Meningitis: 1 to 2 g IV or IM once a day (or in equally divided doses twice a day); Maximum dose: 4 g/day
Uncomplicated gonococcal infections: 250 mg IM as a single dose
Surgical prophylaxis: 1 g IV as a single dose 30 to 120 minutes before surgery Infants and Children (01 month or older): The usual dose is 50 to 75 mg/kg intravenous or intramuscular administration once a day (or in equally divided doses twice a day).
Pneumonia, Bronchitis, Skin and skin structure infection, Urinary tract infections, Bacterial Septicemia, Bone and joint infections: 50 to 75 mg/kg IV or IM once a day (or in equally divided doses twice a day); Maximum dose: 2 g/day
Acute bacterial otitis media: 50 mg/kg IM in single dose; Maximum dose: 1 g/day Meningitis: 100 mg/kg IV or IM in single daily dose or (or in equally divided doses twice a day); Maximum dose: 4 g/day.
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.
Method of administration
Preparation of Solutions for Intravenous/Intramuscular Injections:
For Intramuscular Injection: 250 mg or 500 mg Ceftriaxone should be dissolved in 2 ml Lidocaine HCI 1% injection or 1 g Ceftriaxone in 3.5 ml of Lidocaine HCI 1% injection.
For Intravenous Injection: 250 mg or 500 mg Ceftriaxone should be dissolved in 5 ml of Water for injection or 1 g Ceftriaxone in 10 ml of Water for injection or 2 g Ceftriaxone in 20 ml of Water for injection.
The injection should be administered over 2-4 minutes, by Intravenous/Intramuscular injection or by tubing infusion over a period of 30 minutes at concentration between 10 mg/mL and 40 mg/mL. Before starting treatment through Ceftriaxone injection, patient tolerance test should be checked by administration of a test dose. (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).
Contra-indication
Ceftriaxone should not be given to patients with a history of hypersensitivity to cephalosporin antibiotics.
Warning and precaution
As with other cephalosporins, anaphylactic shock cannot be ruled out even if a thorough patient history is taken. Anaphylactic shock requires immediate countermeasures such as intravenous epinephrine followed by a glucocorticoid. In rare cases, shadows suggesting sludge have been detected by sonograms of the gallbladder. This condition was reversible on discontinuation or completion of Ceftriaxone therapy. Even if such findings are associated with pain, conservative, nonsurgical management is recommended. During prolonged treatment the blood picture should be checked at regular intervals.
Side effects
Ceftriaxone is generally well tolerated. A few side effects such as gastro-intestinal effects including diarrhea, nausea and vomiting, stomatitis and glossitis; cutaneous reactions including rash, pruritus, urticaria, edema and erythema multiforme; hematologic reactions including eosinophilia, thrombocytopenia, leucopenia, anemia and neutropenia; hepatic reactions including elevations of SGOT or SGPT, bilirubinemia; CNS reactions including nervousness, confusion, sleep disturbances, headache, hyperactivity, convulsion, hypertonia and dizziness were reported. Local phlebitis occurs rarely following intravenous administration but can be minimized by slow injections over 2-4 minutes.
Use in pregnancy & lactation
Its safety in human pregnancy has not been established. Therefore, it should not be used in pregnancy unless absolutely indicated. Low concentrations of Ceftriaxone are excreted in human milk. Caution should be exercised when Ceftriaxone is administered to a lactating mother.
Use in children & adolescents
Ceftriaxone must not be given to neonates if the neonates is premature and newborn (up to 28 days of age).
Drug interaction
No drug interactions have been reported.
Overdose
There is no specific antidote. Treatment of overdosage should be symptomatic.
Storage
Keep out of the reach of children. Keep below 300C, protect from light.
Packing
Triforce 500 mg IM Injection: Each combipack contains 1 vial of sterile Ceftriaxone Sodium USP, 1 ampoule of 2 ml Lidocaine Hydrochloride BP 1% Injection, a sterile disposable syringe and an ampoule breaker.
Triforce 1 g IM Injection: Each combipack contains 1 vial of sterile Ceftriaxone Sodium USP, 1 ampoule of 3.5 ml Lidocaine Hydrochloride BP 1% Injection, a sterile disposable syringe and an ampoule breaker.
Triforce 1 g IV Injection: Each combipack contains 1 vial of sterile Ceftriaxone Sodium USP, 1 ampoule of 10 ml Water for Injection BP, a sterile disposable syringe and an ampoule breaker.
Triforce 2 g IV Injection: Each combipack contains 1 vial of Ceftriaxone Sodium USP, 1 ampoule of 20 ml Water for Injection BP, a complementary pouch comprised of a sterile disposable syringe, a butterfly needle, an alcohol pad and a first aid bandage.
