Clavulanate drug data and news

Clavulanate drug data, resources, and news articles (when available). Onconews.org provides news on cancer research. This section, which includes profiles on medicines that may or not be cancer-related is in beta form. If things run smoothly we will be releasing a new format late in the summer of 2006.

Generic name Clavulanate
Brand Names/Synonyms Clavulanate; Clavulanic Acid
Indication For use with Amoxicillin, clavulanic acid is suitable for the treatment of infections with Staph. aureus and Bacteroides fragilis, or with beta-lactamase producing H. influenzae and E. coli.
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Description Not Available
Pharmacology Clavulanic acid, produced by the fermentation of Streptomyces Clavuligerus, is a beta-lactam structurally related to the penicillins. Clavulanic acid is used in conjunction with amoxicillin for the treatment of bronchitis and urinary tract, skin, and soft tissue infections caused by beta-lactamase producing organisms.
Mechanism Of Action Clavulanic acid competitively and irreversibly inhibits a wide variety of beta-lactamases, commonly found in microorganisms resistant to penicillins and cephalosporins. By inactivating beta-lactamase (the bacterial resistance protein), the accompanying penicillin/cephalosporin drugs may be made more potent.
Clavulanate News
(When available)

Orf Virus Infection in Humans—New York, Illinois, California ...  Feb 28, 2006
Routine bacterial cultures were negative. The patient was treated empirically with ciprofloxacin and amoxicillin-clavulanate. On ... - Journal of American Medical Association (subscription),

Par Pharmaceutical Reports Sales and Earnings for 2005  Feb 28, 2006
Par was assigned Ivax Corporation's distribution rights for various dosage forms of the immediate release antibiotics amoxicillin/clavulanate potassium and ... - MSN Money

DSM: Annual Report 2005: Highlights: Life Science Products  Feb 10, 2006
6-APA and 7-ADCA), side chains, semi-synthetic penicillins, semisynthetic cefalosporins and other active ingredients such as potassium clavulanate and nystatin ... - Webbolt Business News (subscription),

GlaxoSmithKline's Topical Antibacterial Retapamulin Accepted for ...  Feb 14, 2006
...meet clinical needs, including the topical antibacterial agent Bactroban® (mupirocin) as well as the oral agent Augmentin® (amoxicillin/clavulanate potassium ... - Yahoo! News (press release)

GlaxoSmithKline's Topical Antibacterial Retapamulin Accepted for ...  Feb 14, 2006
...clinical needs, including the topical antibacterial agent Bactroban(R) (mupirocin) as well as the oral agent Augmentin(R) (amoxicillin/clavulanate potassium). ... - PharmaLive.com (press release),

Dosage Forms Tablets, ER tablets, suspensions
Drug_Category Anti-bacterial Agents; ATC:J01C
Absorption 75%
Interactions The concurrent administration of allopurinol and ampicillin increases substantially the incidence of rashes in patients receiving both drugs as compared to patients receiving ampicillin alone. It is not known whether this potentiation of ampicillin rashes is due to allopurinol or the hyperuricemia present in these patients. In controlled clinical trials of AUGMENTIN XR, 22 patients received concomitant allopurinol and AUGMENTIN XR. No rashes were reported in these patients. However, this sample size is too small to allow for any conclusions to be drawn regarding the risk of rashes with concomitant AUGMENTIN XR and allopurinol use. In common with other broad-spectrum antibiotics, AUGMENTIN XR may reduce the efficacy of oral contraceptives
Toxicity gastrointestinal symptoms including stomach and abdominal pain, vomiting, and diarrhea. Rash, hyperactivity, or drowsiness have also been observed in a small number of patients
Organisms Affected Enteric bacteria and other eubacteria
Chemical IUPAC Name 3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylicacid
Chemical Formula C8H9NO5
Molecular Weight 199.161 g/mol
Smiles String C1C2N(C1=O)C(C(=CCO)O2)C(=O)O
Melting Point 117.5-118 °C
Water Solubility 300 mg/mL (potassium salt)
State Solid
LogP/Hphobicity -0.919
Isoelectric Point Not Available
Biotransformation Hepatic
Half Life 1.0 hour
Protein Binding [%] Low (22 to 30%)
RxList Link Not Available>RXlist
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Drug Reference Not Available
Drug Type Approved Drug
Accession No APRD00049
CAS Registry Number 58001-44-8
KEGG Compound ID C06662
PubChem ID SID:8887
PharmGKB ID Not Available
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] Not Available

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