GENERIC

Ceftriaxone Sodium

Indications

G-Ceftriax injection 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

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%).

Dosage and administration

Adult : The usual dose is 1 to 2 gm 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 gm/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 gm/day

Acute bacterial otitis media : 50 mg/kg IM in single dose; Maximum dose: 1 gm/day

Meningitis : 100 mg/kg IV or IM in single daily dose or (or in equally divided doses twice a day); Maximum dose: 4 gm/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.

Interactions

No drug interactions have been reported.

Contraindications

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

Side effects

G-Ceftriax 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.

Pregnancy and 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.

Precautions and warnings

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 G-Ceftriax 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.

Overdose

There is no specific antidote. Treatment of overdosage should be symptomatic.

Storage

Vial store in a cool, dry place (below 30° C), away from light & moisture. Keep out of the reach of children.

Clinical information is taken from the most complete brand listing (G-Ceftriax); it applies to the active ingredient.

Brands of Ceftriaxone Sodium

Brands of Ceftriaxone Sodium
#BrandCompanyFormStrengthPrice
211RitKemiko Pharmaceuticals Ltd.IM Injection1 gm/vialNot listed
212RitKemiko Pharmaceuticals Ltd.IV Injection1 gm/vialNot listed
213RitKemiko Pharmaceuticals Ltd.IM Injection250 mg/vialNot listed
214RitKemiko Pharmaceuticals Ltd.IV Injection2 gm/vialNot listed
215RitKemiko Pharmaceuticals Ltd.IM Injection500 mg/vialNot listed
216RofecinRadiant Pharmaceuticals Ltd.IV Injection1 gm/vialNot listed
217RofecinRadiant Pharmaceuticals Ltd.IM Injection1 gm/vialNot listed
218RofecinRadiant Pharmaceuticals Ltd.IV Injection2 gm/vialNot listed
219RofecinRadiant Pharmaceuticals Ltd.IV Injection500 mg/vialNot listed
220RofecinRadiant Pharmaceuticals Ltd.IM Injection500 mg/vialNot listed
221TemtrixTeam Pharmaceuticals Ltd.IV Injection1 gm/vialNot listed
222TemtrixTeam Pharmaceuticals Ltd.IM Injection1 gm/vialNot listed
223TemtrixTeam Pharmaceuticals Ltd.IV Injection2 gm/vialNot listed
224TopcefNavana Pharmaceuticals Ltd.IM Injection1 gm/vialNot listed
225TopcefNavana Pharmaceuticals Ltd.IV Injection1 gm/vialNot listed
226TopcefNavana Pharmaceuticals Ltd.IM Injection250 mg/vialNot listed
227TopcefNavana Pharmaceuticals Ltd.IV Injection2 gm/vialNot listed
228TopcefNavana Pharmaceuticals Ltd.IV Injection500 mg/vialNot listed
229TopcefNavana Pharmaceuticals Ltd.IM Injection500 mg/vialNot listed
230TraxMedimet Pharmaceuticals Ltd.IM Injection1 gm/vialNot listed
231TraxMedimet Pharmaceuticals Ltd.IV Injection1 gm/vialNot listed
232TraxMedimet Pharmaceuticals Ltd.IM Injection250 mg/vialNot listed
233TraxMedimet Pharmaceuticals Ltd.IV Injection250 mg/vialNot listed
234TraxMedimet Pharmaceuticals Ltd.IM Injection500 mg/vialNot listed
235TraxMedimet Pharmaceuticals Ltd.IV Injection500 mg/vialNot listed
236TraxefBeacon Pharmaceuticals PLCIV Injection1 gm/vialNot listed
237TraxefBeacon Pharmaceuticals PLCIM Injection250 mg/vialNot listed
238TraxefBeacon Pharmaceuticals PLCIV Injection2 gm/vialNot listed
239TraxefBeacon Pharmaceuticals PLCIM Injection500 mg/vialNot listed
240TraxefBeacon Pharmaceuticals PLCIV Injection500 mg/vialNot listed

This page is general information and is not medical advice. It does not replace a registered doctor, and it is not a prescription or a recommendation to use any medicine or test. Prices are listed prices and may change. Always follow the advice of your doctor or pharmacist.