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thalidomide - Universidade Nova de Lisboa
thalidomide - Universidade Nova de Lisboa

... company The Distillers Company (Biochemicals) Ltd, who marketed thalidomide under the brand name Distavel throughout the United Kingdom, Australia and New Zealand on behalf of Australians born between January 1, 1958 and December 31, 1970. The lead plaintiff in the court case was Ms Lynette Rowe, a ...
Brittney - BIOL 501 Article Summary 5
Brittney - BIOL 501 Article Summary 5

... affected by thalidomide during embryonic development. - However, variable limb truncations such as amelia (absence of limbs) and phocomelia (proximal limb truncations) are most frequent. - Thalidomideinduced limb defects and microphthalmia (small eyes) are caused by an oxidative stress mediated upre ...
T Thalidomide
T Thalidomide

... Nonenzymatic hydrolysis appears to be the principal mechanism of thalidomide breakdown. However, the exact metabolic pathway(s) has not been fully characterized. The precise route of drug excretion is not well defined. ...
Thalidomide - Academics
Thalidomide - Academics

... •Extremely high doses were not fatal nor were other side effects detected in animal testing •Therefore, thalidomide described as “nontoxic” ...
Thalidomide
Thalidomide

... between thalidomide and the horrific birth defects. Thalidomide was finally withdrawn in 1961 (1962 in some countries). ...
Thalidomide
Thalidomide

... Nausea vomiting in pregnancy NVP – 1st trimester (1/3) ...
Thalidomide - World of Teaching
Thalidomide - World of Teaching

... Nausea vomiting in pregnancy NVP – 1st trimester (1/3) ...
The_Thalidomide_Story
The_Thalidomide_Story

... • When do you think most women would be inclined to take this drug? ...
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Development of analogs of thalidomide



The development of analogs of thalidomide was precipitated by the discovery of the anti-angiogenic and anti-inflammatory properties of the drug yielding a new way of fighting cancer as well as some inflammatory diseases after it had been banned in 1961. The problems with thalidomide included; teratogenic side effects, high incidence of other adverse reactions, poor solubility in water and poor absorption from the intestines.In 1998 thalidomide was approved by the US Food and Drug Administration (FDA) for use in newly diagnosed multiple myeloma (MM) under strict regulations. This has led to the development of a number of analogs with fewer side effects and increased potency which include; lenalidomide, (currently marketed), pomalidomide and apremilast (currently marketed), all of which are manufactured by Celgene.
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