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Sildenafil 50 mg for sale in the States of South Africa and Argentina, respectively. For these countries, "Viread" was first authorised for sale in August 2007, after receiving US regulatory approval. The European Commission requires that all therapeutic products under research or clinical development be authorised for sale in Europe prior to approval. late 2012, "Viread' was approved for sale in all EU Member States.
Eligible indications for Viresitan in the United States, where it was first authorised for sale, include the treatment of following conditions: mild to moderate erectile dysfunction (50 70%), pre-ejaculatory latency of the ejaculation (less than 10 days), and premature ejaculation (less than six months). For other indications, the treatment of mild to moderate erectile dysfunction, pre-ejaculatory latency of the ejaculation (less than 10 days), and premature ejaculation are eligible indications as well.
In the United States, minimum age at which to buy Viread for the treatment of erectile dysfunction is 17 years old.
Pfizer issued a press release in October 2012 that the company is planning to initiate a Phase III study of "Viread" in men with premature ejaculation.
The US FDA issued a public advisory in November 2012 regarding the approved indications for sale of Viread (the press release this was posted on Pfizer's website). It is likely that this advisory applies to all licensed worldwide brands of Viread. The public advisory states:
Clinical Studies of 'Viread' are under way in Australia and a Phase III study of 'Viread' in men with premature ejaculation is currently underway in the United States. approval of 'Viread' for sale in the United States will increase its potential for use those patients who have premature ejaculation, but do not have serious medical conditions that would prevent the use of other treatment options. As a result of the approval 'Viread' for sale in the United States, Pfizer expects to make an aggregate payment of approximately $90 million to resolve regulatory assessments of 'Viread' in two additional clinical programs Australia and the United States.
The FDA noted that Pfizer already has a patent for Viread in Australia. The information on patent was published by the Australian patent office and Pfizer has received a licence for use of the Viread patent in United States.
Pfizer does not appear to have an on-going Phase III trial on the treatment of premature ejaculation as there was no further press release issued by the Pfizer after this press release was issued by the FDA in November 2012 about Pfizer plans to initiate generic sildenafil for sale a Phase III trial of Viread in Australia.
On 21 June 2014, Pfizer received a licence from the Australian patent office for use of the Viread patent in United States as of May 2014.
If you would like to read a full report on the clinical safety and efficacy of Viread in the United States, please visit following links:
In the United Kingdom, "Viread" is licensed for approval in the treatment of pre-ejaculatory latency ejaculation (less than 10 days).
In Argentina, "Viread" is licensed for sale in pharmacies sildenafil citrate for sale uk the treatment of mild to moderate erectile dysfunction and pre-ejaculatory latency of the ejaculation (less than 10 days).
The approval of "Viread" in United States is important the medical community as it opens up the opportunity for Viread treatment of erectile dysfunction. The reason given to enable approval in the United States was that "Viread has been shown to be safe and well tolerated for pre-ejaculatory latency of the ejaculation in men any age, no matter whether or not they have prostate cancer, which might a negative effect if man with prostate cancer had to use more treatment online pharmacy degree us options due to delay in effect."
There is a significant concern that Viread may increase the risk for prostate cancer, especially during high dose treatment of this disease. There are no data to indicate that the risk of this would be increased during use of "Viread".
In the United States, Pfizer will likely need to be prepared pay approximately $90 million to resolve regulatory assessments of "Viread" in the United States two additional planned studies in Australia and the United States.
In November 2009 Pfizer agreed to pay $1.3 billion in an antitrust settlement with the US Department of Justice and the Federal Trade Commission (FTC), and paid a $7-million civil penalty based on its marketing practices related to Vioxx. In a joint statement issued by the FTC and Department of Justice announcing the settlement, officials declared: "The record shows that Pfizer committed anticompetitive acts which affected the incentives of its competitors to invest and innovate in order to"
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