Loracarbef
Loracarbef Uses, Dosage, Side Effects, Food Interaction and all others data.
Loracarbef is a carbacephem antibiotic sometimes grouped together with the second-generation cephalosporin antibiotics. It is marketed under the trade name Lorabid.
Loracarbef is considered a second generation cephalosporin antibiotic. The advantages of cephalosporin antibiotics include a broad range of activity, a safe record in children with almost no dose-related toxicity, and the lack of need to monitor levels. Adverse reactions are rare and consist primarily of hypersensitivity reactions with urticaria, nonspecific rash, and pruritus. Loracarbef can be used to treat a large number of bacterial infections caused by gram-negative and gram-positive bacteria, including upper respiratory tract bacterial infections, chronic bronchitis, pneumonia, sinusitis, pharyntitis and tonsillitis, skin absceses, urinary tract infections and pyelonephritis caused by E. coli, S. pyogenes, S. aureus, S. saprphyticus, S. penumoniae, H. influenzae and M. catarrhalis.
Trade Name | Loracarbef |
Availability | Discontinued |
Generic | Loracarbef |
Loracarbef Other Names | Loracarbef, Loracarbefum |
Related Drugs | amoxicillin, prednisone, doxycycline, ciprofloxacin, cephalexin, metronidazole, azithromycin, clindamycin, ceftriaxone, levofloxacin |
Type | Oral |
Formula | C16H16ClN3O4 |
Weight | Average: 349.769 Monoisotopic: 349.082933722 |
Protein binding | 25% |
Groups | Approved, Investigational, Withdrawn |
Therapeutic Class | |
Manufacturer | |
Available Country | United States |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
Used to treat upper respiratory tract bacterial infections, chronic bronchitis, pneumonia, sinusitis, pharyntitis and tonsillitis, skin absceses, urinary tract infections and pyelonephritis caused by E. coli, S. pyogenes, S. aureus, S. saprphyticus, S. penumoniae, H. influenzae and M. catarrhalis.
How Loracarbef works
Loracarbef is an oral, synthetic beta-lactam antibiotic of the carbacephem class. Chemically, carbacephems differ from cephalosporin-class antibiotics in the dihydrothiazine ring where a methylene group has been substituted for a sulfur atom. Loracarbef has a spectrum of activity similar to that of the second generation cephalosporins. It is structurally identical to cefaclor except for a sulfur atom that has been replaced by a methylene group. This change gives greater chemical stability in solution and allows storage at room temperature. Loracarbef, like all b-lactams and cephalosporins, inhibits penicillin binding proteins, enzymes that create the cross-linkage of the peptidoglycan polymer. This binding leads to interference with the formation and remodeling of the cell wall structure.
Toxicity
Adverse effects include diarrhea, nausea, stomach upset, vomiting, headache, dizziness, rash, bone marrow depression.
Food Interaction
- Take on an empty stomach. Food decreases absorption.
[Moderate] ADJUST DOSING INTERVAL: Loracarbef may exhibit reduced gastrointestinal absorption in the presence of food.
When loracarbef capsules were administered with food, the peak plasma concentrations were 50% to 60% of concentrations after administration in a fasting state and were reached 30 to 60 minutes later.
Area under the concentration-time curve (AUC) was not affected.
The therapeutic effect of the antimicrobial may be reduced.
MANAGEMENT: Loracarbef should be administered at least one hour before or two hours after eating.
Loracarbef Drug Interaction
Unknown: brentuximab, brentuximab, doxorubicin, doxorubicin, antihemophilic factor, antihemophilic factor, immune globulin intravenous, immune globulin intravenous, encorafenib, encorafenib, terbutaline, terbutaline, esmolol, esmolol, multivitamin with minerals, multivitamin with minerals, carvedilol, carvedilol, cyclophosphamide, cyclophosphamide
Loracarbef Disease Interaction
Major: colitisModerate: renal dysfunction, dialysis, liver disease
Elimination Route
Well absorbed with approximately 90% absorbed from the gastrointestinal tract after oral ingestion.
Half Life
1 hour. In subjects with moderate impairment of renal function the plasma half-life was prolonged to approximately 5.6 hours.
Innovators Monograph
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