Zydus Lifesciences receives tentative approval from USFDA for Letermovir Tablets
Letermovir tablets are used to prevent disease caused by a virus called cytomegalovirus in people who have received a bone marrow transplant or kidney transplant.;
Ahmedabad: Zydus Lifesciences Limited has announced that the Company has received tentative approval from the United States Food and Drug Administration (USFDA) to market Letermovir tablets, 240 mg and 480 mg, (USRLD: Prevymis tablets).
Letermovir tablets are used to prevent disease caused by a virus called cytomegalovirus (CMV) in people who have received a bone marrow transplant or kidney transplant.
Cytomegalovirus (CMV) is a common virus belonging to the herpesvirus family. It infects people of all ages worldwide. Once infected, the virus remains dormant in the body for life and can reactivate without causing symptoms. CMV spreads through bodily fluids, including saliva, blood, urine, semen, and breast milk. In healthy individuals, CMV infection often causes no noticeable symptoms or only mild symptoms resembling those of the flu, such as fever, fatigue, and muscle aches. However, CMV can cause serious complications in people with weakened immune systems, such as transplant recipients, people living with HIV/AIDS, and infants infected before birth (congenital CMV).
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