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Rocephin is a sterile, broad-spectrum antibiotic injection containing ceftriaxone sodium (a third-generation cephalosporin). This 500 mg vial is formulated for intramuscular (IM) administration after reconstitution with a suitable diluent (usually sterile water for injection or lidocaine solution for IM). It is widely used for the treatment of moderate to severe bacterial infections.
Active ingredient: Ceftriaxone sodium (equivalent to 500 mg ceftriaxone base per vial).
Excipients: Vial contains sterile powder; reconstituted with water for injection or lidocaine (for IM only).
Third-generation cephalosporin antibiotic (β-lactam).
Bactericidal: inhibits bacterial cell wall synthesis.
Powder for solution for injection.
500 mg single-use vial (IM route).
Rocephin is indicated for infections caused by susceptible organisms, including:
Lower respiratory tract infections (pneumonia, bronchitis)
Urinary tract infections (complicated/uncomplicated)
Skin and soft tissue infections
Bone and joint infections
Intra-abdominal infections
Septicemia and bacteremia
Meningitis (higher doses, often IV)
Gonorrhea (single-dose IM therapy)
Surgical prophylaxis (perioperative use)
Adults: 1–2 g once daily (IV/IM), or divided every 12 hours. For certain infections (e.g., gonorrhea), a single IM dose of 250–500 mg is common.
Children: 20–80 mg/kg/day depending on age/severity.
Neonates: Dosing reduced; avoid calcium co-administration.
Renal/Hepatic impairment: Usually no adjustment needed, except in combined severe dysfunction.
Reconstitution for IM: Reconstitute 500 mg vial with 2 mL of 1% lidocaine (reduces pain at injection site).
May cause CNS effects (seizures, encephalopathy), GI upset, and electrolyte imbalance.
No specific antidote; treatment is supportive. Hemodialysis is not very effective due to high protein binding.
If a dose is missed, administer as soon as remembered. Do not double dose. Follow the healthcare provider’s schedule.
Reconstitute powder with recommended diluent (usually 2 mL of 1% lidocaine for IM injection).
Shake until fully dissolved.
Inject deep into a large muscle mass (e.g., gluteal).
Never administer IV solutions with calcium-containing fluids in neonates.
Administer under supervision of healthcare personnel.
Known hypersensitivity to ceftriaxone, cephalosporins, or severe penicillin allergy.
Neonates (≤28 days) requiring calcium IV therapy (risk of precipitation/fatal reaction).
History of severe allergic reaction to β-lactam antibiotics.
Common:
Pain, redness, or swelling at injection site
Diarrhea, nausea, vomiting
Rash, itching
Headache
Serious (rare):
Severe allergic reactions (anaphylaxis)
Clostridium difficile–associated diarrhea
Hemolytic anemia
Liver enzyme elevations, biliary sludging
Seizures (with very high doses/renal impairment)
Administer only under medical supervision.
Monitor renal and hepatic function during prolonged therapy.
Caution in patients with history of severe allergies.
Prolonged use may result in superinfection, including fungal infections.
Do not reconstitute or mix with calcium-containing IV solutions (especially in neonates).
Calcium-containing IV fluids: Contraindicated (risk of precipitation).
Oral anticoagulants (e.g., warfarin): May increase INR — monitor closely.
Aminoglycosides: Additive nephrotoxicity risk.
Chloramphenicol: May antagonize bactericidal effect.
Store powder vials below 25 °C, protected from light.
Use reconstituted solution immediately (stability limited).
Discard unused solution.
Dispose of vials/needles in sharps container per biomedical waste guidelines.
Prescription Only Medicine
Must be administered by healthcare professionals.
Reconstitute only with approved diluent (lidocaine for IM).
Pain at injection site is common; lidocaine helps reduce discomfort.
Complete the full course of therapy, even if symptoms improve.
Report any allergic reactions or severe diarrhea immediately.
Do not self-administer — always seek medical supervision.
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