Image
Group 2373.png

 

Catafast 50mg granules

 

Indication

 

Catafast® 50mg (diclofenac potassium) is indicated for post-operative inflammation and pain following orthopedic surgery.1

 

 

Dosage

 

  • The recommended dose is 50 mg 2-3 times daily in divided doses.1

 

Efficacy

 

In a double-blind study, the investigator rated diclofenac dispersible as excellent for 55% of the patients, good for 35%, and fair for only 10%. In comparison, ketorolac was rated as excellent for 16% of patients, good for 72%, and fair for 12%.2 

Diclofenac dispersible demonstrated significantly superior efficacy over ketorolac in reducing postoperative pain starting from the 15-minute time point post-dose, with an estimated treatment difference of 9.0 mm (p = 0.01) in the intent-to-treat dataset and 8.13 mm (p = 0.005) in the acceptable patient dataset. After six hours, 62% of patients treated with diclofenac (n = 29) experienced complete pain relief compared to 42% of those treated with ketorolac (n = 26).2

 

Image
Group 2358.png

 

Pharmacokinetics

 

  • Catafast® is quickly absorbed due to its buffering formulation.1*
  • Mean peak plasma concentrations of 1.6 micrograms attained after 5 to 20 minutes after ingestion of one sachet of 50 mg.2

 

* Combined with potassium salt of diclofenac.1

 

SVG

For Catafast® Abbreviated prescribing information

PDF

References

  1. Catafast® 50 mg Egyptian Drug Authority approved insert leaflet, Approval date:7/11/2023.

  2. Fineschi G, Tamburrelli FC, Francucci  BM,  Pisati R. Oral Diclofenac Dispersible Provides a Faster Onset of Analgesia than Intramuscular Ketorolac in the Treatment of Postoperative Pain.  Clinical Drug Investigation. 1997;13:1–7

Approved by Egyptian Drug Authority: HF0082OA4734/092025. Invalidation date: 01/09/2027.
Kindly report any violated online promotional, educational and awareness material not having this message to The General administration for Regulation of Marketing & Advertising Materials at: www.edaegypt.gov.eg

Image
Ortho QR Code

HF0082OA4734/092025
01/09/2027

 

        

Adverse Events Reporting

We encourage using the following Electronic reporting tool for reporting into the safety database directly:
If the electronic reporting tool is not working - please use the following: https://www.report.novartis.com
1 - Generic Mailbox: [email protected]
2 - CISCO: +20 2 2 2861000: Press 3 for Adverse Events Reporting