Mezlocillin Sodium
A to Z Drug Facts
Mezlocillin Sodium |
(MEZZ-low-SILL-in SO-dee-uhm) |
Mezlin |
Class: Antibiotic/penicillin |
Action Inhibits biosynthesis of bacterial cell wall mucopeptide.
Indications Treatment of infections of lower respiratory tract, urinary tract, skin or skin structure; intra-abdominal infections; uncomplicated gonorrhea; gynecological infections; septicemia; streptococcal infections; severe infections; and pseudomonas infections caused by susceptible strains of specific microorganisms and prophylaxis.
Contraindications Hypersensitivity to penicillins.
ADULTS: IM/IV 200 to 300 mg/kg/day in 4 to 6 divided doses. Usual doses are 3 g q 4 hr or 4 g q 6 hr. IM doses should not exceed 2 g/injection. CHILDREN > 1 MO to < 12 YR: IM/IV 50 mg/kg q 4 hr. NEONATES: IV 75 mg/kg q 6 to 12 hr.
Contraceptives, oral: May reduce efficacy of oral contraceptives. Tetracyclines: May impair bactericidal effects of mezlocillin. INCOMPATIBILITIES: Parenteral aminoglycosides may inactivate aminoglycosides in vitro; o not mix in same IV solution.
Lab Test Interferences Antiglobulin (Coombs') test: Drug may cause false-positive results in certain patient groups. Urine glucose test: Drug may cause false-positive results with copper sulfate tests (eg, Benedict test, Fehling test, or Clinitest tablets); enzyme-based tests (eg, Clinistix, Tes-tape) are not affected. Urine protein determinations: Drug may cause false-positives with sulfosalicylic acid and boiling test, acetic acid test, biuret reaction and nitric acid test; bromphenol blue test (Multi-Stix) not affected.
CNS: Neurotoxicity (eg, lethargy, neuromuscular irritability, hallucinations, convulsions, seizures); dizziness; fatigue; insomnia; reversible hyperactivity; rolonged muscle relaxation. DERM: Ecchymosis. EENT: Itchy eyes. GI: Nausea; vomiting; abdominal pain or cramp; diarrhea or bloody diarrhea; ectal bleeding; flatulence; enterocolitis; pseudomembranous colitis; anorexia. GU: Interstitial nephritis (oliguria, proteinuria, hematuria, hyaline casts, pyuria); nephropathy; elevated creatinine or BUN. HEPA: Transient hepatitis; cholestatic jaundice. HEMA: Anemias; thrombocytopenia; eosinophilia; leukopenia; granulocytopenia; eutropenia; bone marrow depression; agranulocytosis; reduced hemoglobin or hematocrit; prolongation of bleeding time and PT; altered blood cell counts. META: Elevated serum alkaline phosphatase; hypernatremia; reduced serum potassium, albumin, total proteins, and uric acid. OTHER: Hypersensitivity reactions that may lead to death; vaginitis; hyperthermia; ain at site of injection; deep vein thrombosis; hematomas; vein irritation; hlebitis; sciatic neuritis.
Pregnancy: Category B. Lactation: Excreted in breast milk. Bleeding abnormalities: Hemorrhagic manifestations associated with abnormalities of coagulation tests (bleeding time, PT, platelet aggregation) may occur. Abnormalities should revert to normal when drug is discontinued. Hypersensitivity: Reactions range from mild to life threatening. Administer cautiously to cephalosporin-sensitive patients because of possible cross reactivity. Pseudomembranous colitis: Consider in patients with diarrhea. Sodium content: 1.85 mEq sodium/g. Superinfection: May result in bacterial or fungal overgrowth of nonsusceptible organisms.
PATIENT CARE CONSIDERATIONS |
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Copyright © 2003 Facts and Comparisons
David S. Tatro
A to Z Drug Facts