0
Kuntz and keller type
Wiki User
∙ 13y ago
Add your answer:
Earn +20 pts
What are the two forms of technology?
Two forms of technology used today are computers and cell phones. The average household family of four might have 3 cell phones and 2 or more computer devices, depending on the age of the children.
What are two main forms of treatment used by psychologists?
The two main forms of treatment used by psychologists are insight and behavioral.
What two forms of punctuation can be used to create compound sentences?
Two forms of punctuation that can be used to create compound sentences are commas (,) and semicolons (;).
Do you write out the word or write the number when using o'clock?
Both forms are commonly used: 2 o'clock and two o'clock.See related link.Both forms are commonly used: 2 o'clock and two o'clock.See related link.Both forms are commonly used: 2 o'clock and two o'clock.See related link.Both forms are commonly used: 2 o'clock and two o'clock.See related link.
What were the two forms of writing used by the Egyptians and Mesopotamians and which used which?
The Egyptians used hieroglyphics and the Mesopotamians used cuneiform.
Was thalidomide man made?
THE FIRST CONTRIBUTOR ARGUED: Thalidomide was man-made by the two inventors called Dr.W.Kunz and Dr.H.Keller. This appalling drug was made in Germany. THIS CONTRIBUTOR CALLS HIMSELF THE SECOND CONTRIBUTOR AND REPLIES: A distinction should be made between the thalidomide drug and the thalidomide scandal. Yes, the thalidomide DRUG was man-made But not necessarily in Germany. It may have been made in the United States of America, France or even the United Kingdom of Northern Ireland and Great Britain. (1) The thalidomide SCANDAL was however government-made. BEFORE 10 APRIL 2010, THE SECOND CONTRIBUTOR KNEW THAT The regulators allowed thalidomide on the market in 1957. At a 30 April - 1 May 1960 Düsseldorf Congress of neurologists, neurologist Dr Ralf Voss warned that thalidomide attacks the nervous system of the mother. The regulators did not do anything and it was up to the manufacturer of thalidomide, Chemie Grünenthal in Stolberg, Aachen, to withdraw thalidomide from the market on 27 November 1961, that's eighteen months after the warning that thalidomide attacks the nervous system of the mother. (2) ON 10 APRIL 2010 On 10 April 2010, the French daily Le Monde reported that thalidomide was withdrawn in December 1961 and that two years before that date, many German doctors warned that thalidomide attacked the nervous system of the mother. (3) This would mean that the thalidomide alarm was raised in December 1959. And the regulators let it on the market until December 1961. That's twenty-four months, right? THE STORY GOES The story goes that a young Canadian-born doctor, named Frances Oldham Kelsey, managed to convince the USA Food and Drug Administration (FDA) not to allow thalidomide, known in the USA as "kevadon", into the USA. The problem with this story is that Kelsey was only appointed to the FDA in 1960 (4) and that, oh wonder, the first drug she had to examine at the FDA was ... kevadon. That examination of thalidomide by FDA bureaucrat Kelsey started on 12 September 1960 (4 and 5). That examination thus started after the 30 April - 1 May 1960 Düsseldorf warning. (And the real thalidomide warning was in December 1959, says Le Monde.) THE STORY THEN CONTINUES Dr. Frances Kelsey, then a medical officer with the fledgling Food and Drug Administration, [...] shows immense courage by staunchly refusing to grant permission for the release of the medication in the United States. She does so despite enormous pressure both from her superiors and the American pharmaceutical company that has MILLIONS OF THALIDOMIDE TABLETS READY FOR MASS DISTRIBUTION. But for her, a calamity of unprecedented magnitude, a consequence of, " …gigantic marketing plans…" and an "…absence of scientific discipline…" would have been inevitable. [capitalisation by the second contributor.] (6) The second contributor asks: Did the so-called regulators in the countries where thalidomide had been allowed also have millions of thalidomide tablets ready for mass distribution and does that explain why these so-called regulators NEVER reacted to the December 1959 warning, by removing thalidomide from the market, but let the heroes from Chemie Grünenthal in Stolberg, Aachen take the initiative of that withdrawal in December 1961? CONCLUSION The thalidomide scandal was made by guv'mints to justify or legitimate their welfare states. Or was the drug really woman-made in 1938 by Frances Oldham Kelsey? (7) No distinction should then be made between the thalidomide drug and the thalidomide scandal?
Was thalidomide man-made?
THE FIRST CONTRIBUTOR ARGUED: Thalidomide was man-made by the two inventors called Dr.W.Kunz and Dr.H.Keller. This appalling drug was made in Germany. THIS CONTRIBUTOR CALLS HIMSELF THE SECOND CONTRIBUTOR AND REPLIES: A distinction should be made between the thalidomide drug and the thalidomide scandal. Yes, the thalidomide DRUG was man-made But not necessarily in Germany. It may have been made in the United States of America, France or even the United Kingdom of Northern Ireland and Great Britain. (1) The thalidomide SCANDAL was however government-made. BEFORE 10 APRIL 2010, THE SECOND CONTRIBUTOR KNEW THAT The regulators allowed thalidomide on the market in 1957. At a 30 April - 1 May 1960 Düsseldorf Congress of neurologists, neurologist Dr Ralf Voss warned that thalidomide attacks the nervous system of the mother. The regulators did not do anything and it was up to the manufacturer of thalidomide, Chemie Grünenthal in Stolberg, Aachen, to withdraw thalidomide from the market on 27 November 1961, that's eighteen months after the warning that thalidomide attacks the nervous system of the mother. (2) ON 10 APRIL 2010 On 10 April 2010, the French daily Le Monde reported that thalidomide was withdrawn in December 1961 and that two years before that date, many German doctors warned that thalidomide attacked the nervous system of the mother. (3) This would mean that the thalidomide alarm was raised in December 1959. And the regulators let it on the market until December 1961. That's twenty-four months, right? THE STORY GOES The story goes that a young Canadian-born doctor, named Frances Oldham Kelsey, managed to convince the USA Food and Drug Administration (FDA) not to allow thalidomide, known in the USA as "kevadon", into the USA. The problem with this story is that Kelsey was only appointed to the FDA in 1960 (4) and that, oh wonder, the first drug she had to examine at the FDA was ... kevadon. That examination of thalidomide by FDA bureaucrat Kelsey started on 12 September 1960 (4 and 5). That examination thus started after the 30 April - 1 May 1960 Düsseldorf warning. (And the real thalidomide warning was in December 1959, says Le Monde.) THE STORY THEN CONTINUES Dr. Frances Kelsey, then a medical officer with the fledgling Food and Drug Administration, [...] shows immense courage by staunchly refusing to grant permission for the release of the medication in the United States. She does so despite enormous pressure both from her superiors and the American pharmaceutical company that has MILLIONS OF THALIDOMIDE TABLETS READY FOR MASS DISTRIBUTION. But for her, a calamity of unprecedented magnitude, a consequence of, " …gigantic marketing plans…" and an "…absence of scientific discipline…" would have been inevitable. [capitalisation by the second contributor.] (6) The second contributor asks: Did the so-called regulators in the countries where thalidomide had been allowed also have millions of thalidomide tablets ready for mass distribution and does that explain why these so-called regulators NEVER reacted to the December 1959 warning, by removing thalidomide from the market, but let the heroes from Chemie Grünenthal in Stolberg, Aachen take the initiative of that withdrawal in December 1961? CONCLUSION The thalidomide scandal was made by guv'mints to justify or legitimate their welfare states. Or was the drug really woman-made in 1938 by Frances Oldham Kelsey? (7) No distinction should then be made between the thalidomide drug and the thalidomide scandal?
What are two amerindians words?
Two Amerindian words still used today
What forms of energy are used when you are bouncing on a trampoline?
there are two types of energy used when on a trampoline and they are kinetic and gravitational
If Thalidomide use was stopped in 1961 why were my little brother and another girl I know both born in the US in late 1963 with identical genital and visual thalidomide birth defects?
Thalidomide was never approved for use in the United States. NEVER! So, first, one must determine if the two individuals you mentioned have been officially diagnosed by a physician as having genital and visual birth defects that are caused ONLY BY THALIDOMIDE and (a) not caused by another medication or (b) not congenital in nature.Second, if congenital birth defects and other medications have been ruled out as causative, then one must remember that, simply because a medication is no longer being manufactured or dispensed, it continues to be available for an unknown period of time in the homes of those for whom it was prescribed or who purchased it prior to the date when sales and manufacturing ceased.Therefore, IF the birth defects have been definitively identified as being related to Thalidomide, then the mother of each child must have had access to Thalidomide via her own individual supply or from the supply of someone else.To further complicate matters, Thalidomide was ALSO USED IN COMBINATION with other medications to treat conditions such as migraine and asthma, making it much less likely that someone who was using such a combination product would be AWARE of the potential danger.In all cases, the medication would have originated from a country other than the United States because, as already noted, no Thalidomide products were ever approved for sale in the United States.In summary, in 1961, the manufacturing, dispensing, and sale of Thalidomide and Thalidomide-containing combination products was stopped. The USE of these products continued because of the medication that was already in the hands of the public.Regrettably, any continued use may have been partly attributable to the public not having been fully educated in 1961 regarding the risks of Thalidomide and Thalidomide-containing combination products. This is especially true for U.S. citizens who may have received one of these products when traveling outside of the United States.
What is a white crystalline solid having two isomeric forms used in dyes?
naphthol
Is two plus two one?
In the most widely used forms of arithmetic, two plus two is four, not one. However, in some forms of advanced mathematical systems, two plus two might end up being one, or even zero.
