Diflunisal

Diflunisal
Systematic (IUPAC) name
2',4'-difluoro-4-hydroxybiphenyl-3-carboxylic acid
Clinical data
AHFS/Drugs.com monograph
MedlinePlus a684037
Pregnancy cat. C(AU) C(US)
Legal status POM (UK) -only (US)
Routes Oral
Pharmacokinetic data
Bioavailability 80-90%
Protein binding >99%
Metabolism Hepatic
Half-life 8 to 12 hours
Excretion Renal
Identifiers
CAS number 22494-42-4 Y
ATC code N02BA11
PubChem CID 3059
DrugBank APRD00922
ChemSpider 2951 Y
UNII 7C546U4DEN Y
KEGG D00130 Y
ChEBI CHEBI:39669 Y
ChEMBL CHEMBL898 Y
Chemical data
Formula C13H8F2O3 
Mol. mass 250.198 g/mol
SMILES eMolecules & PubChem
 N(what is this?)  (verify)

Diflunisal is a non-steroidal anti-inflammatory drug (NSAID). It was developed by Merck Sharp & Dohme in 1971 after showing promise in a research project studying more potent chemical analogs of aspirin.[1] It was first sold under the brand name Dolobid, marketed by Merck & Co., but generic versions are now widely available. It is available in 250 mg and 500 mg tablets.

Contents

Mechanism

Like all NSAIDs, diflunisal acts by inhibiting the production of prostaglandins,[2] hormones which are involved in inflammation and pain. Diflunisal also has an antipyretic effect, but this is not a recommended use of the drug. Though diflunisal has an onset time of 1 hour, and maximum analgesia at 2 to 3 hours, the plasma levels of diflunisal will not be steady until repeated doses are taken. The long plasma half-life is a distinctive feature of diflunisal in comparison to similar drugs. To increase the rate at which the diflunisal plasma levels become steady, a loading dose is usually used. It is primarily used to treat symptoms of arthritis, and for acute pain following oral surgery, especially removal of wisdom teeth.

Effectiveness of diflunisal is similar to other NSAIDs, but the duration of action is twelve hours or more.[3] This means fewer doses per day are required for chronic administration. In acute use, it is popular in dentistry when a single dose after oral surgery can maintain analgesia until the patient is asleep that night.

Side effects

The inhibition of prostaglandins has the effect of decreasing the protection given to the stomach from its own acid. Like all NSAIDS, this leads to an increased risk of stomach ulcers, and their complications, with long-term use.

Gastrointestinal

Cardiovascular

Ear, nose, throat, and eye

Central nervous system

Skin

Overdose

Deaths that have occurred from diflunisal usually involved mixed drugs and or extremely high dosage. The oral LD50 is 500 mg/kg. Symptoms of overdose include coma, tachycardia, stupor, and vomiting. The lowest dose without the presence of other medicines which caused death was 15 grams. Mixed with other medicines, a death at 7.5 grams has also occurred. Diflunisal usually comes in 250 or 500 mg, making it is relatively hard to overdose by accident.

Indications

Contraindications

Cautions

References

  1. ^ Adams, S. S. (1999). "Ibuprofen, the propionics and NSAIDs: Personal reflections over four decades". Inflammopharmacology 7 (3): 191–197. doi:10.1007/s10787-999-0002-3. PMID 17638090.  edit
  2. ^ Wallace, J. L. (2008). "Prostaglandins, NSAIDs, and Gastric Mucosal Protection: Why Doesn't the Stomach Digest Itself?". Physiological Reviews 88 (4): 1547. doi:10.1152/physrev.00004.2008. PMID 18923189. http://physrev.physiology.org/content/88/4/1547.full.  edit
  3. ^ http://www2.cochrane.org/reviews/en/ab007440.html

External links