Source: Health Products Regulatory Authority (IE) Revision Year: 2021 Publisher: Sanofi-aventis Ireland Ltd., T/A SANOFI, Citywest Business Campus, Dublin 24
Lasix 20mg/2ml Solution for Injection or Infusion.
Pharmaceutical Form |
---|
Solution for Injection or Infusion. Clear, colourless aqueous solution. |
Furosemide 20mg in 2ml aqueous solution.
For excipients, see 6.1.
Active Ingredient | Description | |
---|---|---|
Furosemide |
Furosemide inhibits active chloride transport in the thick ascending limb. Re-absorption of sodium, chloride from the nephron is reduced and a hypotonic or isotonic urine produced. The evidence from many experimental studies suggests that furosemide acts along the entire nephron with the exception of the distal exchange site. |
List of Excipients |
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Water for Injection |
Type I, PhEur glass ampoules in packs of 5 × 2ml glass ampoules.
Sanofi-aventis Ireland Ltd., T/A SANOFI, Citywest Business Campus, Dublin 24
PA 540/52/2
1st April 1977 / 1st January 2006
Drug | Countries | |
---|---|---|
LASIX | Austria, Australia, Brazil, Canada, Cyprus, Germany, Ecuador, Estonia, Hong Kong, Croatia, Ireland, Italy, Japan, Lithuania, Mexico, Netherlands, New Zealand, Singapore, Turkey, United States, South Africa |
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