Drug Wyeth Pharmaceutical Assistance - In considering drug Wyeth pharmaceutical assistance, Wyth Pharmaceuticals has taken a firm stand defending the safety of its depression medication Efexor. In this article, we take moment to examine what the company has said about drug Wyeth pharmaceutical assistance and the effectiveness of Efexor. Of course, if you are interested in obtaining more information about drug Wyeth pharmaceutical assistance, we strongly suggest that you contact the company directly.
Here is what Wyeth has had to say about Efexor in recent days:
“wyeth Pharmaceuticals has affirmed the safety and efficacy of its depression treatment Efexor after UK regulators announced their decision to revise the labeling for the drug. Wyeth (NYSE: WYE - news) said that it would challenge the decision.
“wyeth Pharmaceuticals has affirmed the safety and efficacy of its depression treatment Efexor after UK regulators announced their decision to revise the labeling for the drug. Wyeth said that it would challenge the decision.
“the Medicine and Healthcare Products Regulatory Agency (MHRA) has requested provisional labeling for Efexor in the UK indicating that treatment should only be initiated under specialist care with starting doses limited to 75mg.
“the labeling is also set to show that the products are indicated for moderate to severe patients, that a baseline ECG is recommended for new patients and that the products are contraindicated in patients with preexisting cardiovascular disease.
“the MHRA’s provisional action stems from, among other factors, its view that Efexor could be associated with disruption of the heart rhythm, and could be associated with severe reactions following abrupt discontinuation.
“additionally, the regulator reviewed publications relying on data from the Office of National Statistics (ONS), which suggest that Efexor is associated with a rate of fatal overdose significantly higher than selective serotonin reuptake inhibitors (SSRIs), but significantly lower than the rate associated with tricyclic antidepressants (TCAs).
“wyeth’s analyses of the ONS report using the UK’s general practice research database (GPRD) found that physicians prescribed Efexor to patients who on average had more risk factors for suicide than patients who were prescribed certain SSRIs. This is not unexpected since in clinical practice Efexor is frequently used when other agents (SSRIs, TCAs) have been ineffective.”
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