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Brand Name :
Iwazac
Synonyms :
bendazac
Class :
Ophthalmological, Non-steroidal Anti-inflammatory agents
Dosage Forms & StrengthsÂ
Topical CreamÂ
0.5%Â
Topical OintmentÂ
0.5%Â
Â
Several times a day, the affected area receives a suitable amount of this substance administered to it.
Ophthalmic Drops
Two drops in each eye, three times a day, or half of a single dose.
Use two drops in each eye of the multi-dose eye thrice daily.
Safety and efficacy not establishedÂ
Refer adult dosingÂ
When bendazac is used together with piroxicam, this leads to enhanced risk or seriousness of adverse outcomes
When melitracen is used together with bendazac, this leads to increased risk or seriousness of gastrointestinal bleeding
When bendazac is used together with proglumetacin, this leads to enhanced risk or seriousness of adverse events
When bendazac is used together with bufexamac, this leads to enhanced risk or seriousness of adverse events
When bendazac is used together with benoxaprofen, this leads to enhanced risk or seriousness of adverse events
When bendazac is used together with nifenazone, this leads to enhanced risk or seriousness of adverse events
When bendazac is used together with difenpiramide, this leads to increased risk or seriousness of adverse events
etoricoxib: it may decrease the excretion rate of bendazac
Actions and Spectrum:Â
bendazac exerts its anti-inflammatory and analgesic effects by inhibiting the synthesis of prostaglandins. Prostaglandins are chemical messengers in the body crucial to the inflammatory response. They are produced by the enzyme cyclooxygenase (COX), specifically the COX-1 and COX-2 isoforms.
Bendazac inhibits the activity of both COX-1 and COX-2 enzymes, thereby reducing the production of prostaglandins. This action leads to a decrease in inflammation, pain, and other associated symptoms.Â
bendazac’s spectrum of activity is primarily limited to treating certain skin conditions. It is commonly used in dermatology to manage inflammatory skin disorders such as contact dermatitis, eczema, and other forms of dermatitis. The drug is typically applied topically as a cream or gel directly to the affected area, allowing it to exert its anti-inflammatory effects locally.Â
Frequency not definedÂ
Skin irritationÂ
Dryness and PeelingÂ
PhotosensitivityÂ
Black box warning:Â
NoneÂ
Contraindications/caution:Â
Contraindications:Â
Caution:Â
Pregnancy consideration: Insufficient data availableÂ
Lactation: Excretion of the drug in human breast milk is unknownÂ
Pregnancy category:Â
Category A: well-controlled and Satisfactory studies show no risk to the fetus in the first or later trimester.Â
Category B: there was no evidence of risk to the fetus in animal studies, and there were not enough studies on pregnant women.Â
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.   Â
Category D: adequate data with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.   Â
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.   Â
Category N: There is no data available for the drug under this categoryÂ
Pharmacology:Â
Pharmacokinetics:Â
AbsorptionÂ
When administered as its lysine salt in a 500 mg oral tablet, bendazac is well absorbed into the human body. bendazac’s maximum plasma concentration (Cmax) ranges from 35 to 55 mg/L.Â
DistributionÂ
With a volume of distribution (Vd) of 0.16 L/kg, bendazac’s apparent distribution throughout the body is relatively low. A lower Vd value suggests that the drug remains primarily in the plasma and does not extensively distribute into tissues.Â
MetabolismÂ
bendazac is extensively metabolized in the body. More than 60% of an administered dose is excreted in the urine as the hydroxylated primary metabolite 5-hydroxybendazac and its glucuronide. The hydroxylation process likely involves adding a hydroxyl group (-OH) to the parent compound bendazac, forming 5-hydroxybendazac.Â
Elimination and ExcretionÂ
Approximately 60% of a dose of bendazac is eliminated via the urine as its primary metabolite, 5-hydroxybendazac. Additionally, approximately 15% of the administered dose is eliminated in the urine as unchanged bendazac and glucuronide. The plasma elimination half-life recorded for bendazac is 1.7 to 5.2 hours, with a mean of 3.5 hours. The plasma clearance of bendazac is recorded as 0.018 to 0.054 L/h/kg, with a mean of 0.033 L/h/kg.Â
Administration:Â
Patient information leafletÂ
Generic Name: bendazacÂ
Why do we use bendazac?Â
bendazac is a non-steroidal anti-inflammatory drug (NSAID) primarily used for its anti-inflammatory and analgesic properties. It is commonly used in dermatology to treat various inflammatory skin conditions. Some of the primary uses of bendazac include:Â