this is insane ......FDA Recommend To Stop Darvon and Darvocet Marketing

[Guest guest]

why ??? not even one death ,only due to abnormal heart rhythms ????

 

but its o.k. to shoot up kids with rounds and rounds  OF VACCINATIONs  

FDA Recommend To Stop Darvon and Darvocet Marketing

on December 27, 2010 — Leave a Comment

One of the pain killer medicine we know is Darvon and Darvocet. Darvon and

Darvocet will stop marketing the drugs after new studies from FDA showed they

can create abnormal heart rhythms even at normal doses,on  The Wall Street

Journal reported Nov. 20.

Propoxyphene is an active ingredient in Darvon. This drug firstly marketed in

1957. Darvocet contains propoxyphene and acetaminophen. Darvon and Darvocet were

developed by Eli Lilly & Company. Now, generic drugs companies, such as Xanodyne

Pharmaceuticals and Qualitest/Vintage Pharmaceuticals, produce them instead.

What makes Darvon and Darvocet is dangerous is the chemical inside the drug,

that is propoxyphene (the generic name for Darvon; Darvocet includes that

ingredient plus acetaminophen) raises the risk of dangerous heart rhythm

changes.

The result of this study about Darvon and Darvocet is when customer taken

recommended dosages, propoxyphene can significantly change the electrical

activity of the heart. With using electrocardiogram it can be detected and may

increase an individual’s chances of heart rhythm abnormalities. The side

effect

of darvon chemical is dehydration, changes in medication, kidney problems,  and

other minor modifications in a patient’s health.

For this problem, Xanodyne agreed to remove Darvon and Darvocet from the drug

market, and the FDA will ask other drug producer to follow it. Now, many drug

containing propoxyphene are already being removed from the European Union,

following recommendation from the European Medicines Agency in 2009.

Image : http://www.rxlist.com

[Guest guest]

why ??? not even one death ,only due to abnormal heart rhythms ????

 

but its o.k. to shoot up kids with rounds and rounds  OF VACCINATIONs  

FDA Recommend To Stop Darvon and Darvocet Marketing

on December 27, 2010 — Leave a Comment

One of the pain killer medicine we know is Darvon and Darvocet. Darvon and

Darvocet will stop marketing the drugs after new studies from FDA showed they

can create abnormal heart rhythms even at normal doses,on  The Wall Street

Journal reported Nov. 20.

Propoxyphene is an active ingredient in Darvon. This drug firstly marketed in

1957. Darvocet contains propoxyphene and acetaminophen. Darvon and Darvocet were

developed by Eli Lilly & Company. Now, generic drugs companies, such as Xanodyne

Pharmaceuticals and Qualitest/Vintage Pharmaceuticals, produce them instead.

What makes Darvon and Darvocet is dangerous is the chemical inside the drug,

that is propoxyphene (the generic name for Darvon; Darvocet includes that

ingredient plus acetaminophen) raises the risk of dangerous heart rhythm

changes.

The result of this study about Darvon and Darvocet is when customer taken

recommended dosages, propoxyphene can significantly change the electrical

activity of the heart. With using electrocardiogram it can be detected and may

increase an individual’s chances of heart rhythm abnormalities. The side

effect

of darvon chemical is dehydration, changes in medication, kidney problems,  and

other minor modifications in a patient’s health.

For this problem, Xanodyne agreed to remove Darvon and Darvocet from the drug

market, and the FDA will ask other drug producer to follow it. Now, many drug

containing propoxyphene are already being removed from the European Union,

following recommendation from the European Medicines Agency in 2009.

Image : http://www.rxlist.com