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Flustar Brand names, Flustar Analogs

Flustar Brand Names Mixture

  • No information avaliable

Flustar Chemical_Formula


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Flustar fda sheet

Flustar msds (material safety sheet)

Flustar MSDS

Flustar Synthesis Reference

No information avaliable

Flustar Molecular Weight

250.198 g/mol

Flustar Melting Point

210-221 oC

Flustar H2O Solubility

Practically insoluble (14.5 mg/L) at neutral or acidic pH.

Flustar State


Flustar LogP


Flustar Dosage Forms

Tablets for oral administration (250 mg or 500 mg)

Flustar Indication

For acute or long-term use for symptomatic treatment of mild to moderate pain, osteoarthritis, and rheumatoid arthritis.

Flustar Pharmacology

Diflunisal is a nonsteroidal drug with analgesic, anti-inflammatory and antipyretic properties. It is a peripherally-acting non-narcotic analgesic drug. Habituation, tolerance and addiction have not been reported. Diflunisal is a difluorophenyl derivative of salicylic acid. Chemically, diflunisal differs from aspirin (acetylsalicylic acid) in two respects. The first of these two is the presence of a difluorophenyl substituent at carbon 1. The second difference is the removal of the 0-acetyl group from the carbon 4 position. Diflunisal is not metabolized to salicylic acid, and the fluorine atoms are not displaced from the difluorophenyl ring structure.

Flustar Absorption

Rapidly and completely absorbed following oral administration, with a bioavailability of 80-90%.

Flustar side effects and Toxicity

Oral LD50 in rat, mouse, and rabbit is 392 mg/kg, 439 mg/kg, and 603 mg/kg, respectively. Symptoms of overdose include coma, tachycardia, stupor, and vomiting. The lowest dose without the presence of other medicines which caused death was 15 grams.

Flustar Patient Information

Flustar Organisms Affected

Humans and other mammals