Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | 2C16H17N3O5S.H2O |
| Molecular Weight | 744.792 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 6 / 6 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.CC1=C(N2[C@H](SC1)[C@H](NC(=O)[C@H](N)C3=CC=C(O)C=C3)C2=O)C(O)=O.CC4=C(N5[C@H](SC4)[C@H](NC(=O)[C@H](N)C6=CC=C(O)C=C6)C5=O)C(O)=O
InChI
InChIKey=AJAMDISMDZXITN-QXBGZBSVSA-N
InChI=1S/2C16H17N3O5S.H2O/c2*1-7-6-25-15-11(14(22)19(15)12(7)16(23)24)18-13(21)10(17)8-2-4-9(20)5-3-8;/h2*2-5,10-11,15,20H,6,17H2,1H3,(H,18,21)(H,23,24);1H2/t2*10-,11-,15-;/m11./s1
Cefadroxil is a new semisynthetic cephalosporin with a broad antibacterial spectrum and a high chemotherapeutic potential when administered orally. Many studies have established the efficacy of the administration of once- or twice-daily cefadroxil in the management of infections in the respiratory tract, urinary tract, skin and soft tissues, and bones and joints.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2354204 Sources: https://www.ncbi.nlm.nih.gov/pubmed/7447421 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Curative | DURICEF Approved UseCefadroxil is indicated for the treatment of patients with infection caused by susceptible strains of the designated organisms in the following diseases:
Urinary tract infections caused by E. coli, P. mirabilis, and Klebsiella species.
Skin and skin structure infections caused by staphylococci and/or streptococci.
Pharyngitis and/or tonsillitis caused by Streptococcus pyogenes (Group A beta-hemolytic streptococci). Launch Date1978 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
17.9 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/7073267/ |
500 mg single, oral dose: 500 mg route of administration: Oral experiment type: SINGLE co-administered: |
CEFADROXIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
50.8 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/7073267/ |
500 mg single, oral dose: 500 mg route of administration: Oral experiment type: SINGLE co-administered: |
CEFADROXIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
1.2 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/7073267/ |
500 mg single, oral dose: 500 mg route of administration: Oral experiment type: SINGLE co-administered: |
CEFADROXIL plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
Doses
| Dose | Population | Adverse events |
|---|---|---|
50 mg/kg 2 times / day steady, oral Dose: 50 mg/kg, 2 times / day Route: oral Route: steady Dose: 50 mg/kg, 2 times / day Sources: |
unhealthy, 2 days -15 years Health Status: unhealthy Age Group: 2 days -15 years Sex: M+F Sources: |
Other AEs: Rash, Itching... Other AEs: Rash (1.5%) Sources: Itching (1.5%) Pruritus (1.5%) Nausea (7.5%) Vomiting (7.5%) Diarrhoea (7.5%) |
50 mg/kg 2 times / day steady, oral Dose: 50 mg/kg, 2 times / day Route: oral Route: steady Dose: 50 mg/kg, 2 times / day Sources: |
unhealthy, 2 days -15 years Health Status: unhealthy Age Group: 2 days -15 years Sex: M+F Sources: |
Disc. AE: Diarrhoea... AEs leading to discontinuation/dose reduction: Diarrhoea (severe, 2 patients) Sources: |
15 mg/kg 2 times / day steady, oral Dose: 15 mg/kg, 2 times / day Route: oral Route: steady Dose: 15 mg/kg, 2 times / day Sources: |
unhealthy, 6 months - 12 years Health Status: unhealthy Age Group: 6 months - 12 years Sex: M+F Sources: |
Other AEs: Vomiting... |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Itching | 1.5% | 50 mg/kg 2 times / day steady, oral Dose: 50 mg/kg, 2 times / day Route: oral Route: steady Dose: 50 mg/kg, 2 times / day Sources: |
unhealthy, 2 days -15 years Health Status: unhealthy Age Group: 2 days -15 years Sex: M+F Sources: |
| Pruritus | 1.5% | 50 mg/kg 2 times / day steady, oral Dose: 50 mg/kg, 2 times / day Route: oral Route: steady Dose: 50 mg/kg, 2 times / day Sources: |
unhealthy, 2 days -15 years Health Status: unhealthy Age Group: 2 days -15 years Sex: M+F Sources: |
| Rash | 1.5% | 50 mg/kg 2 times / day steady, oral Dose: 50 mg/kg, 2 times / day Route: oral Route: steady Dose: 50 mg/kg, 2 times / day Sources: |
unhealthy, 2 days -15 years Health Status: unhealthy Age Group: 2 days -15 years Sex: M+F Sources: |
| Diarrhoea | 7.5% | 50 mg/kg 2 times / day steady, oral Dose: 50 mg/kg, 2 times / day Route: oral Route: steady Dose: 50 mg/kg, 2 times / day Sources: |
unhealthy, 2 days -15 years Health Status: unhealthy Age Group: 2 days -15 years Sex: M+F Sources: |
| Nausea | 7.5% | 50 mg/kg 2 times / day steady, oral Dose: 50 mg/kg, 2 times / day Route: oral Route: steady Dose: 50 mg/kg, 2 times / day Sources: |
unhealthy, 2 days -15 years Health Status: unhealthy Age Group: 2 days -15 years Sex: M+F Sources: |
| Vomiting | 7.5% | 50 mg/kg 2 times / day steady, oral Dose: 50 mg/kg, 2 times / day Route: oral Route: steady Dose: 50 mg/kg, 2 times / day Sources: |
unhealthy, 2 days -15 years Health Status: unhealthy Age Group: 2 days -15 years Sex: M+F Sources: |
| Diarrhoea | severe, 2 patients Disc. AE |
50 mg/kg 2 times / day steady, oral Dose: 50 mg/kg, 2 times / day Route: oral Route: steady Dose: 50 mg/kg, 2 times / day Sources: |
unhealthy, 2 days -15 years Health Status: unhealthy Age Group: 2 days -15 years Sex: M+F Sources: |
| Vomiting | 9 patients | 15 mg/kg 2 times / day steady, oral Dose: 15 mg/kg, 2 times / day Route: oral Route: steady Dose: 15 mg/kg, 2 times / day Sources: |
unhealthy, 6 months - 12 years Health Status: unhealthy Age Group: 6 months - 12 years Sex: M+F Sources: |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Multi-objective optimization of an industrial penicillin V bioreactor train using non-dominated sorting genetic algorithm. | 2007-10-15 |
|
| Fluorescence studies of the dehydration of cefadroxil monohydrate. | 2007-10 |
|
| In vitro activity of cefadroxil, cephalexin, cefatrizine and cefpirome in presence of essential and trace elements. | 2007-10 |
|
| DRESS syndrome from cefadroxil confirmed by positive patch test. | 2007-10 |
|
| A comparative study of capillary zone electrophoresis and pH-potentiometry for determination of dissociation constants. | 2007-09-03 |
|
| Idiopathic granulomatous mastitis masquerading as carcinoma of the breast: a case report and review of the literature. | 2007-07-27 |
|
| Impact of genetic knockout of PEPT2 on cefadroxil pharmacokinetics, renal tubular reabsorption, and brain penetration in mice. | 2007-07 |
|
| Do physician outcome judgments and judgment biases contribute to inappropriate use of treatments? Study protocol. | 2007-06-07 |
|
| Determination of beta-lactam antibiotics in milk using micro-flow chemiluminescence system with on-line solid phase extraction. | 2007-06-05 |
|
| Human oral drugs absorption is correlated to their in vitro uptake by brush border membrane vesicles. | 2007-05-04 |
|
| Symptomatic relapse of group A beta-hemolytic streptococcal tonsillopharyngitis in children. | 2007-05 |
|
| Hydrates and solid-state reactivity: a survey of beta-lactam antibiotics. | 2007-05 |
|
| Determination of cefquinome in pig plasma and bronchoalveolar lavage fluid by high-performance liquid chromatography combined with electrospray ionization mass spectrometry. | 2007-05 |
|
| Demonstration of functional dipeptide transport with expression of PEPT2 in guinea pig cardiomyocytes. | 2007-03 |
|
| Species distribution and properties of staphylococci from canine dermatitis. | 2007-02 |
|
| Choroid plexus epithelial monolayers--a cell culture model from porcine brain. | 2006-12-21 |
|
| Generalizability in two clinical trials of Lyme disease. | 2006-10-17 |
|
| Development of a Health-Related Quality of Life Questionnaire (HRQL) for patients with Extremity Soft Tissue Infections (ESTI). | 2006-10-11 |
|
| Flow injection chemiluminescence determination of cefadroxil using potassium permanganate and formaldehyde system. | 2006-09-18 |
|
| Treatment of lichen sclerosus with antibiotics. | 2006-09 |
|
| Medication use for pediatric upper respiratory tract infections. | 2006-08 |
|
| European Surveillance of Antimicrobial Consumption (ESAC): outpatient cephalosporin use in Europe. | 2006-08 |
|
| Molecular interactions between dipeptides, drugs and the human intestinal H+ -oligopeptide cotransporter hPEPT1. | 2006-07-01 |
|
| Chemiluminescence flow-injection analysis of beta-lactam antibiotics using the luminol-permanganate reaction. | 2006-06-23 |
|
| Chiral separation of cefadroxil by capillary electrochromatography. | 2006-06-16 |
|
| Positive effect of natural and negatively charged cyclodextrins on the stabilization of penicillins towards beta-lactamase degradation due to inclusion and external guest-host association. An NMR and MS study. | 2006-04-07 |
|
| Determination of cefadroxil by sequential injection with spectrophotometric detector. | 2006-04 |
|
| Cephalosporins can be prescribed safely for penicillin-allergic patients. | 2006-02 |
|
| Quantitative structure/activity relationship modelling of pharmacokinetic properties using genetic algorithm-combined partial least squares method. | 2006 |
|
| Urinary bactericidal activity of oral antibiotics against common urinary tract pathogens in an ex vivo model. | 2006 |
|
| PEPT2 (Slc15a2)-mediated unidirectional transport of cefadroxil from cerebrospinal fluid into choroid plexus. | 2005-12 |
|
| A sensitive assay of amoxicillin in mouse serum and broncho-alveolar lavage fluid by liquid-liquid extraction and reversed-phase HPLC. | 2005-09-15 |
|
| Functional expression of the peptide transporter PEPT2 in the mammalian enteric nervous system. | 2005-09-12 |
|
| Presumed pituitary abscess without infectious source treated successfully with antibiotics alone. | 2005-09 |
|
| Heterogeneity of the IgE response to allergenic determinants of cefaclor in serum samples from patients with cefaclor-induced anaphylaxis. | 2005-06 |
|
| Bactericidal activity of oral beta-lactam antibiotics in plasma and urine versus isogenic Escherichia coli strains producing broad- and extended-spectrum beta-lactamases. | 2005-06 |
|
| Interaction of 31 beta-lactam antibiotics with the H+/peptide symporter PEPT2: analysis of affinity constants and comparison with PEPT1. | 2005-01 |
|
| Staphylococcal skin infections in children: rational drug therapy recommendations. | 2005 |
|
| Molecularly imprinted solid phase extraction-pulsed elution-mass spectrometry for determination of cephalexin and alpha-aminocephalosporin antibiotics in human serum. | 2004-11-15 |
|
| Antimicrobial susceptibility of skin-colonizing S. aureus strains in children with atopic dermatitis. | 2004-10 |
|
| The use of a monolithic column to improve the simultaneous determination of four cephalosporin antibiotics in pharmaceuticals and body fluids by HPLC after solid phase extraction--a comparison with a conventional reversed-phase silica-based column. | 2004-09-25 |
|
| Synthesis, characterization and electronic spectra of cefadroxil complexes of d-block elements. | 2004-08 |
|
| Comparative bioavailability of two cefadroxil products using serum and urine data in healthy human volunteers. | 2004-07 |
|
| Direct visualization of peptide uptake activity in the central nervous system of the rat. | 2004-06-24 |
|
| Physician behaviour for antimicrobial prescribing for paediatric upper respiratory tract infections: a survey in general practice in Trinidad, West Indies. | 2004-06-14 |
|
| Minimum inhibitory concentrations for 25 selected antimicrobial agents against Dichelobacter nodosus and Fusobacterium strains isolated from footrot in sheep of Portugal and Spain. | 2004-06 |
|
| Antimicrobial resistance in Escherichia coli in urine samples from children and adults: a 12 year analysis. | 2004-04 |
|
| Meta-analysis of cephalosporin versus penicillin treatment of group A streptococcal tonsillopharyngitis in children. | 2004-04 |
|
| Comparison of trimethoprim-sulfamethoxazole, cephadroxil and cefprozil as prophylaxis for recurrent urinary tract infections in children. | 2004-02 |
|
| The importance of Bi-Digital O-Ring Test in the treatment of multiple hepatic abscesses: a case history. | 2003 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.drugs.com/pro/cefadroxil.html
Cefadroxil tablets are acid-stable and may be administered orally without regard to meals. Administration with food may be helpful in diminishing potential gastrointestinal complaints occasionally associated with oral cephalosporin therapy.
Adults
Urinary Tract Infections
For uncomplicated lower urinary tract infections (i.e., cystitis) the usual dosage is 1 or 2 g per day in a single (q.d.) or divided doses (b.i.d.). For all other urinary tract infections the usual dosage is 2 g per day in divided doses (b.i.d.).
Skin and Skin Structure Infections
For skin and skin structure infections the usual dosage is 1 g per day in single (q.d.) or divided doses (b.i.d.).
Pharyngitis and Tonsillitis
Treatment of group A beta-hemolytic streptococcal pharyngitis and tonsillitis – 1 g per day in single (q.d.) or divided doses (b.i.d.) for 10 days.
Children
For urinary tract infections, the recommended daily dosage for children is 30 mg/kg/day in divided doses every 12 hours. For pharyngitis, tonsillitis, and impetigo, the recommended daily dosage for children is 30 mg/kg/day in a single dose or in equally divided doses every 12 hours. For other skin and skin structure infections, the recommended daily dosage is 30 mg/kg/day in equally divided doses every 12 hours. In the treatment of beta-hemolytic streptococcal infections, a therapeutic dosage of Cefadroxil tablets should be administered for at least 10 days.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/848939
Cefadroxil very effectively inhibited a broad spectrum of gram-positive and gram-negative organisms with MIC (minimal inhibitory concentration) values less than 125 ug/ml.
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NCI_THESAURUS |
C357
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ACTIVE MOIETY
SUBSTANCE RECORD