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Description
A., Lally, J
It is licensed in the United States (under the brand name Egrifta) for HIV-associated lipodystrophy but has not been approved by the MHRA for any indication
After 3 days, cell viability was determined using the CCK-8 cell viability
There is an acute phase comprising emetic episodes occurring during the first 24 h, which is highly susceptible to 5-HT 3 receptor antagonists, and a subsequent delayed phase lasting 25 days, which is thought to also involve SP and inflammatory mediators
