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Ketoprofen

Catalog No. DB01009 Name DrugBank
CAS Number 22071-15-4 Website http://www.ualberta.ca/
M. F. C16H14O3 Telephone (780) 492-3111
M. W. 254.28056 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 882

SYNONYMS

IUPAC name
2-(3-benzoylphenyl)propanoic acid
IUPAC Traditional name
ketoprofen
Brand Name
Toprec
Orugesic
Kefenid
Oscorel
Alrheumun
Capisten
Dexal
Fastum
Iso-K
Ketopron
Lertus
Menamin
Meprofen
Orudis
Oruvail
Actron
Alrheumat
Epatec
Orudis KT
Profenid
Toprek
Synonyms
m-Benzoylhydratropic acid

DATABASE IDS

PubChem CID 3825
CAS Number 22071-15-4
PubChem SID 46505715

PROPERTIES

Hydrophobicity(logP) 3.2
Solubility 51 mg/L

DETAILS

Description (English)
Item Information
Drug Groups approved
Description Ketoprofen, a propionic acid derivative, is a nonsteroidal anti-inflammatory agent (NSAIA) with analgesic and antipyretic properties.
Indication For symptomatic treatment of acute and chronic rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, primary dysmenorrhea and mild to moderate pain associated with musculotendinous trauma (sprains and strains), postoperative (including dental surgery) or postpartum pain.
Pharmacology Ketoprofen is a nonsteroidal anti-inflammatory agent (NSAIA) with analgesic and antipyretic properties. Ketoprofen has pharmacologic actions similar to those of other prototypical NSAIDs, which inhibit prostaglandin synthesis. Ketoprofen is used to treat rheumatoid arthritis, osteoarthritis, dysmenorrhea, and alleviate moderate pain.
Toxicity LD50=62.4 mg/kg (rat, oral).

Symptoms of overdose include drowsiness, vomiting and abdominal pain.


Side effects are usually mild and mainly involved the GI tract. Most common adverse GI effect is dyspepsia (11% of patients). May cause nausea, diarrhea, abdominal pain, constipation and flatulence in greater than 3% of patients.

Affected Organisms
Humans and other mammals
Biotransformation Rapidly and extensively metabolized in the liver, primarily via conjugation to glucuronic acid. No active metabolites have been identified.
Absorption Ketoprofen is rapidly and well-absorbed orally, with peak plasma levels occurring within 0.5 to 2 hours.
Half Life Conventional capsules: 1.1-4 hours

Extended release capsules: 5.4 hours due to delayed absorption (intrinsic clearance is same as conventional capsules)

Protein Binding 99% bound, primarily to albumin
Elimination In a 24 hour period, approximately 80% of an administered dose of ketoprofen is excreted in the urine, primarily as the glucuronide metabolite.
Clearance * Oral-dose cl=6.9 +/- 0.8 L/h [Ketoprofen Immediate-release capsules (4 × 50 mg)]
* Oral-dose cl=6.8 +/- 1.8 L/h [Ketoprofen Extended-release capsules (1 × 200 mg)]
* 0.08 L/kg/h
* 0.7 L/kg/h [alcoholic cirrhosis patients]
References
Kantor TG: Ketoprofen: a review of its pharmacologic and clinical properties. Pharmacotherapy. 1986 May-Jun;6(3):93-103. [Pubmed]
Mazieres B: Topical ketoprofen patch. Drugs R D. 2005;6(6):337-44. [Pubmed]
External Links
Wikipedia
RxList
PDRhealth
Drugs.com

REFERENCES

  • Mazieres B: Topical ketoprofen patch. Drugs R D. 2005;6(6):337-44. Pubmed
  • Kantor TG: Ketoprofen: a review of its pharmacologic and clinical properties. Pharmacotherapy. 1986 May-Jun;6(3):93-103. Pubmed