Decision on Truvada currently on hold by FDA

Truvada drug manufactured by Gilead Sciences is still to get the approval of FDA as a preventive option in high risk HIV individuals. Many researchers and analysts are of a positive view with this drug's approval.
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Fontana, CA ( June 16, 2012 - The decision on Truvada, an anti-HIV medication produced by the drug manufacturer Gilead Sciences has been currently put on hold for three about 3 months by the FDA (Food and Drug Administration).
The reason for appreciation by the FDA is being the use of the drug as a preventive HIV therapeutic remedy, which is first of its kind in the history of medical science. Whereas, analyst are of a positive view with respect to its approval and claim that the approval of this miracle drug by the Gilead Science is predictable as a significant scientific implication.
The drug which has gained a lot of popularity in its clinical trials and analysis as an first line of preventive approach for individuals not affected with HIV but belong to the high risk group of acquiring the disease such as the partners of those afflicted with HIV.
Ira Loss, an analyst in Washington claimed that the extension on the verdict of the drug by the FDA from being mistreated is only delaying its expected activity of this medication as an effective drug. Currently the target date for approval of Truvada by FDA has been extended to September 14 of this year.

An advisory panel conducted last month shed light on the effective measures of this drug and its significance in protecting the high risk individuals from acquiring the condition as well as cease the use of other precautionary measures such as the use of condoms, etc.
It also claimed that the drug needs to be taken daily with care and in case not taken on a daily basis; there exists a concern about the person developing resistance to the drug. Gilead also said that offering condoms, education as well as free HIV testing will be conducted as a part to enhance the use of drug properly.
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