Ken Blackwell

How often does the Food and Drug Administration advise Americans to deliberately take an overdose? Apparently, only when the drug in question is something the good people at Planned Parenthood want to sell over the counter. That's the conclusion that comes to mind after reviewing the Food and Drug Administration's decision late last year to allow the "morning after pill" – also called Plan B – to be sold to people over age 18 in pharmacies without a prescription.

Plan B is basically a pill package that contains five times the typical dose of an oral contraceptive. It is a remedy for a faulty memory (or perhaps, as often happens, condom failure). A woman (or girl, since Planned Parenthood makes these drugs and devices available to children as young as 11 or 12 years old) takes the Plan B regimen within 72 hours after "unprotected" intercourse to prevent pregnancy. Also labeled "emergency contraception," the drug's greatest utility may really be in those situations where the user "forgot" to take the wiser action of forgoing sex outside of marriage.

More than anything else, Plan B offered over the counter, or OTC, is a social experiment. There are many reasons for this. The drug is a social experiment because this method of delivering a potent hormone raises a number of questions to which the FDA gave short shrift. First, despite its moniker as "contraception," the high doses of hormone delivered by Plan B not only prevent ovulation and inhibit conception, but they also help render the wall of a woman's uterus inhospitable to a developing human life after conception has occurred. This mode of action has long been understood to be abortifacient. No one, however, will catch Planned Parenthood telling young women where to get their "emergency occasional abortifacient."

The package insert with detailed information on Plan B does contain this information, but it is found in the fine print that often gets little attention when a drug has been certified by the government as safe for wider use. Surely safety means that a drug has been tested by its manufacturer (in this case, Barr Laboratories) for its effects on people when taken on multiple occasions. That has not been done with Plan B in the United States because its styling as an "emergency" medicine implies that girls and women won't resort to it as a regular means of preventing pregnancy. A trial in which women took the drug three or four times a year for five years would be unethical, since there are clearly healthier ways to avoid sexual contact and pregnancy (although the People's Republic of China has reportedly conducted such trials and the state of New York will fund Medicaid recipients to deploy Plan B up to six times a year).


Ken Blackwell

Ken Blackwell, a contributing editor at Townhall.com, is a senior fellow at the Family Research Council and the American Civil Rights Union and is on the board of the Becket Fund for Religious Liberty. He is the co-author of the bestseller The Blueprint: Obama’s Plan to Subvert the Constitution and Build an Imperial Presidency, on sale in bookstores everywhere..
 
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