Is Bush Interested in Preventing Unwanted Pregnancies?
This is from the Center for Reproductive Rights:
The Center for Reproductive Rights today urged the Bush administration to reconcile its recently stated position on contraception with the five-year long refusal by the Food and Drug Administration to make Plan B, known as the "morning-after pill," available without a prescription. After keeping silent on the subject of contraception for more than one year, the administration conveyed in a letter to Representative Carolyn B. Maloney (D-NY) that it supports “...safe and effective products and services to assist responsible adults in making decisions about preventing or delaying conception."
Despite this view, the Bush administration has taken no constructive action to compel the FDA to increase access to Plan B – a safe and effective medication proven to reduce the risk of pregnancy by approximately 89 percent when it is taken within 72 hours of unprotected intercourse, according to a study published in Obstetrics and Gynecology.
"It is long past time for the FDA to stop the delays, obfuscation and outright refusal to acknowledge what basic science demonstrates," said Nancy Northup, President of the Center for Reproductive Rights in a letter sent today to President Bush. Ms. Northup urged Mr. Bush to put its position on contraception to the test and direct the FDA to immediately approve Plan B for over-the-counter use, "If the administration indeed supports safe and effective products and services to assist responsible adults in making decisions about preventing or delaying conception, then there is no reason for its failure to support the availability of emergency contraception."
Since 2001, medical, public health, and reproductive rights organizations have been requesting that the FDA to make the "morning-after pill" available without a prescription. Unfortunately, for years, the agency has dragged its feet and deployed procedural roadblocks rather than make a decision on the matter. Last month, the agency finally denied the Center for Reproductive Rights' citizen's petition for granting emergency contraception over-the-counter status.
Every 10.5 seconds, an unplanned pregnancy occurs in the United States--an estimated three million such pregnancies every year. And each year, 1.29 million end in abortion. Researchers at the Guttmacher Institute, a nonprofit reproductive health research organization, have concluded that better access to emergency contraception could prevent half of those pregnancies, including those that now end in abortion. Had the FDA approved emergency contraceptives for over-the-counter use when we submitted the citizen's petition, many of the 16 million unplanned pregnancies--and subsequent abortions--that occurred in the five years since could have been avoided.
The Center for Reproductive Rights filed a lawsuit in January 2005 in federal court against the Acting Commissioner of the FDA for failing to approve the emergency contraceptive product Plan B for over-the-counter status. The case is in the discovery phase in the trial court, and was brought on behalf of the Association of Reproductive Health Professionals (ARHP), the National Latina Institute for Reproductive Health, and individuals from a grassroots advocacy group, the MAP (Morning-After Pill) Conspiracy.
6 Comments:
Um, does anyone else see any problem with the White House pressuring the FDA what drugs they should approve?
You're joking, right? If you've been following the politics behind the Morning After Pill, you wouldn't be asking such a stupid question.
Did you follow any of the campaigning by the religion right on HPV.
No, you're just a reactionary who gets off on posting negative comments.
Of course I'm joking, and of course it's perfectly reasonable to expect non-medical experts in the White House to control what drugs the FDA approves -- you know, that place where guys with actual medical degrees work. Sorry, I guess my reactionary disposition has affected my ability to tell jokes.
You must have a short term memory:
Read this article about the former head of the FDA, remember the guy appointed by Bush who was accused of sodomizing his wife. Yeah, that's the guy I want deciding whether I deserve to take the morning after pill.
http://www.thenation.com/doc/20050530/mcgarvey
I won't hold my breath.
Well, I don't know or care much about the guy's alleged sex quirks any more than I care about what he says about Christianity (reference Bill Clinton). But according to The Nation's article he's been cited as one of the best women's doctors in the country. I just don't see why anyone would think Bush has the knowledge or expertise to dictate drug policy to the FDA.
While Andrea Yates's defense team argued about whether or not she was sane when she drowned her five children, medical experts told reporters that patients, like Andrea Yates, are not adequately warned about the powerful and potentially dangerous effects of antidepressant drugs.
In November 2005, more than four years after the Andrea Yates tragedy, the FDA and Wyeth pharmaceuticals agreed to warn patients and their doctors about the risk of homicidal thoughts in relation to Effexor XR, an antidepressant Yates was taking when she drowned her five children.
According to drug expert, Professor James O'Donnell PharmD, and Moira Dolan M.D. of the Medical Accountability Network, the warning is buried so deep in the prescription information that nobody is likely to read it.
http://releases.usnewswire.com/GetRelease.asp?id=68954
Post a Comment
<< Home