The US Drug Watchdog is not a Fan
To say that the US Drug Watchdog doesn’t like Darvocet or Darvon would be a huge understatement. Look at what they recently said about Darvocet:"We cannot even begin to say how big of a deal the Darvocet, or Darvon pain pill recalls are. With 22 million US users of Darvocet, Darvon, or their generic version propoxyphene, we fear there are 100,000′s of Americans, who have either had a heart attack, or heart rhythm issues, and we need to get them identified."
As if that wasn’t enough, they went on to say “the saddest thing is, we now believe thousands of US citizens have needlessly died from massive, or fatal heat attacks, and their families will never know it was Darvocet or Darvon because the death occurred in the 1980′s, 1990′s, or early 2000′s."
Darvocet and Darvon Locked and Loaded with Side Effects
In a move that came better late than never, the FDA recalled Darvocet and Darvon. This came in November of 2010, four years after consumer group Public Citizen raised concerns about the drug, and five years after the U.K. banned the drug.This recall came because of a study funded by the FDA which found that Darvocet carried a substantial risk of heart abnormalities, heart arrhythmia, heart electrical changes, suicides, and overdoses.
No comments:
Post a Comment