Ultrapime Injection 500 mg/vial contains Cefepime Hydrochloride, a fourth-generation cephalosporin antibiotic designed for the treatment of serious bacterial infections caused by susceptible organisms. This injectable formulation is highly effective against a broad spectrum of Gram-positive and Gram-negative bacteria, including strains resistant to other cephalosporins.
Cefepime, the active ingredient in Ultrapime Injection, offers potent antibacterial activity by inhibiting bacterial cell wall synthesis, ultimately causing cell lysis and death. The drug is particularly effective in hospital-acquired infections, severe community-acquired infections, and complicated infections that require rapid intravenous therapy. Ultrapime Injection is administered parenterally, providing rapid and reliable therapeutic levels for critically ill patients.
This antibiotic is commonly used in settings where oral therapy is inadequate, or when high tissue concentrations are required to manage severe infections such as septicemia, pneumonia, urinary tract infections, and intra-abdominal infections.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Fourth-generation Cephalosporin – Parenteral Antibiotic
Ultrapime Injection 500 mg/vial is indicated for the treatment of infections caused by susceptible microorganisms, including:
Severe lower respiratory tract infections: Community-acquired and hospital-acquired pneumonia
Complicated urinary tract infections (UTIs): Including pyelonephritis
Skin and soft tissue infections: Caused by susceptible Gram-positive and Gram-negative bacteria
Intra-abdominal infections: As part of combination therapy with metronidazole
Septicemia and bacteremia: Where rapid systemic antibiotic therapy is required
Febrile neutropenia: In immunocompromised patients at risk of bacterial infections
Cefepime is often preferred in serious infections caused by Pseudomonas aeruginosa, Enterobacter spp., Escherichia coli, and Klebsiella pneumoniae, including strains producing beta-lactamases.
Cefepime Hydrochloride is a beta-lactam antibiotic that interferes with bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs). This action leads to inhibition of peptidoglycan cross-linking, resulting in bacterial cell death.
Spectrum of Activity: Broad-spectrum, effective against both Gram-positive (e.g., Staphylococcus aureus, Streptococcus pneumoniae) and Gram-negative bacteria (e.g., E. coli, Klebsiella spp., Pseudomonas spp.).
Resistance Profile: Stable against many beta-lactamases produced by Gram-negative bacteria, including some strains resistant to third-generation cephalosporins.
Pharmacokinetics:
Administered intravenously (IV) or intramuscularly (IM)
Widely distributed in body tissues and fluids, including lungs, kidneys, and bile
Approximately 85% excreted unchanged in urine via glomerular filtration and tubular secretion
Half-life: 2 hours in patients with normal renal function
Inhibits bacterial cell wall synthesis by binding to PBPs
Causes bacterial lysis and death
Provides rapid bactericidal activity against susceptible pathogens
Adults:
Mild to moderate infections: 500 mg IV/IM every 12 hours
Severe infections or immunocompromised patients: 1–2 g IV every 8–12 hours depending on infection severity and renal function
Pediatric Patients:
Dosage is based on body weight and severity of infection; generally, 50 mg/kg IV/IM every 12 hours
Renal Impairment:
Dose adjustment is necessary for patients with creatinine clearance <60 mL/min to avoid drug accumulation and toxicity
Administration Notes:
Reconstitute with sterile water for injection, 0.9% sodium chloride, or dextrose solution
Administer IV slowly over 3–5 minutes or by IV infusion over 30 minutes
IM administration should be done using a suitable muscle site, avoiding intradermal injection
Hypersensitivity to cefepime, other cephalosporins, or beta-lactam antibiotics
History of severe allergic reaction to penicillins
Common adverse reactions include:
Gastrointestinal disturbances: nausea, vomiting, diarrhea
Local reactions: pain, inflammation at injection site
Rare reactions: rash, urticaria, fever, eosinophilia
Neurotoxicity: Seizures may occur in patients with severe renal impairment if dosage is not adjusted
Use with caution in patients with renal impairment, as dose adjustments are necessary
Monitor for signs of Clostridium difficile-associated diarrhea during prolonged therapy
Cross-reactivity may occur in patients with penicillin allergy
Monitor for hematologic changes, liver enzyme elevations, and nephrotoxicity during extended treatment
Pregnancy Category B: Animal studies have not demonstrated risk; limited human data available
Caution is advised during lactation as cefepime is excreted in breast milk
Store at 20–25°C, protected from light
Keep vials in a dry place, out of reach of children
Reconstituted solution should be used immediately or stored under recommended conditions.
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