Non News: Plan B Morning After Pill Does Not Work Well for Big Girls

The European manufacturer of Norlevo, which is their version of Plan B  (Levonorgestrel) has very kindly decided to warn people that their product does not work for women over 176 lbs, and is less effective for women over 165 lbs.

Thanks, HRA Pharma.

Check out the new warning in the Norlevo Package insert for yourself.  It discourages women over 75 Kg from relying on the drug.

This comes under the “told you so” dept. of Pharm information.  In fact, people ALSO could learn here that the newer morning after pill, Ella (ulipristal acetate) has the same problem

All of this  is obvious to those who pay attention to how drugs are designed.   Pharmer has openly warned people for years not to expect good efficacy for birth control pills designed for 130lb women  t0 be as efficacious in women who are much larger.

The U.S. recently moved the  snake oil drug, Plan B, over the counter.   Perhaps this was a crony capitalist effort to help manufacturers snap up as much profit as they could before the general news came out that the drug is not reliable for any women, and really worthless for the larger set.

It appears that Mother Jones is the first of the mainstream media to let the kitty out of the bag in the United States.  They note that the average weight of American girls is 166.2 lbs, which puts them over the weight limit for Plan B to  work at its touted 60 percent effectiveness.   The avg weight of Black and Hispanic women from 20-39 years of age is 186 lbs, which means that they can completely forget about Plan B.

Any hospital or clinic  using  this drug as a part of rape treatment is therefore pushing ineffective treatment and  charging fraudulently.   Planned Parenthood and its ilk are doing the same.

Pharmer’s favorite and oft cited birth control researcher, Anna Glasier, sent up a warning flare in 2011. Click on her effort to identify the groups for which morning after pills do not work.

The American manufacturers have not put out this warning in their product package inserts yet.   Please help your female friends  who will be paying $50 bucks for this drug at the pharmacy,  to understand that Plan B One-Step, Next Choice One Dose, My Way, and various generic one and two pill packs of levonorgestrel morning after pills are fairly worthless as birth control, and when they do work, can have an objectionable mechanism that operates AFTER fertilization.    (As a practical matter,  any perverts who are abusing underaged girls ought to be made aware of this too, so that at least one aspect of the abuse might cease.)

Noting that these hormone analogs have weight dependent efficacy, how much should women be relying on the daily or continuously administered birth control drugs????

Who is REALLY waging the war on women, who remain the  medical underclass????

Related: The low information guys weigh in.
A comprehensive review of Planned Parenthood’s Plan B Scam

 

Is Plan B Worthy of Pharmacy Shelf Space?

Now that whacky Judge Korman has removed the morning after pill, Plan B or Plan B One-Step from pharmacist purview altogether, it might therefore be treated by the pharmacists as an unhealthy thing, not to be sold in pharmacy environments at all. There are various over the counter products which are regarded by us to be ineffective and/or deleterious quack remedies, not worthy of being associated with any health care practice. Tobacco, ma huang (Ephedra sinica), and bitter orange have been deleted from the stock of pharmacies for health reasons. Many pharmacists have relegated homeopathic remedies to the trash heap, on account of the infinitesimal chance that the recipient might be ingesting or applying  an active medicinal ingredient.
The levonorgestrel in Plan B (U.S.)  and Levonelle (U.K),  is likely the least reliable hormonal birth control drug on the market.  It’s less than 60 percent effective per use, and is in a race with ulipristal acetate, or Ella, to the bottom.  Repeated reliance on this drug is likely to soon result in pregnancy, with the embryonic baby clinging to life, awash in an unbalanced mix of hormones.  Might not pharmacists be doing their patients a favor by telling them that this drug is too much of an unreliable, (and unethical)  mess to be used for birth control?

Life Dynamics and Jill Stanek: Groundbreaking Legal Means to Stop Child Predators

As many pro-lifers know, Jill Stanek has joined with Life Dynamics to report news on the life issues. She’s now reporting on a groundbreaking push by Life Dynamics to hold the abortion industry accountable for concealing the sexual abuse of minors.
This blog has repeatedly referred to the first study, done more than 10 years ago by Life Dynamics, which revealed that over 90 percent of abortion clinics, who were called by an actress portraying a 13 year old girl with 22 year old boyfriend, showed a willingness to flout the laws requiring reporting of suspected sexual abuse of minors. Many of these abortion clinics even provided the methodology to conceal the sexual abuse.
Now Life Dynamics has mailed CDs to 53 thousand personal injury attorneys to educate them on the state laws pertinent to this issue, and the possibility of bringing suit against school officials, health care professionals and clinics which provide services to minors who have been sexually abused by adults, and fail in their legal requirement to report such abuse to the state.
Jill Stanek reports that Mark Crutcher’s phone at Life Dynamics has been ringing incessantly ever since launching this campaign.

Your friendly Pharmer suggests that further rich ground for the lawyers exists and that fear of litigation can dissuade retail pharmacies from stocking Plan B and Ella.

The government can force retailers to sell these drugs to the sexual predators, only if they stock the drug.
In the future, lawsuits might be the tool to stop the government from forcing retailers to stock these drugs. None of the businesses could survive a group of civil lawsuits for aiding sexual predators.

Currently good target states for this kind of litigation are Washington, Oregon and of course, New York. The large retail pharmacy chains would run screaming to the State Boards of Pharmacy for relief from the governments requirement to sell these drugs to minor females and their rapists.

Life Dynamics Facebook Announcement of the Campaign to Educate Personal Injury Attorneys.

WND Article explains Life Dyanamics Campaign to Legally Restrain the Enablers of Child Sex Abuse

 

(Another) Pharmacist Refuses to Sell Morning After Pill to a Man

Quite a significant number of pharmacists prefer to sell the morning after pills only to the actual patient.  If you search the net, you’ll find a fair number of stories detailing this phenomenon.

Apparently a recent story has made the news and has a bit of buzz on the blogs. Seems that “Hilary and Jon” had a desire for the morning after pill. They’re not yet married, and apparently not ready to have a baby. Jon was surprised to encounter a female pharmacist who would not sell the drug to him.

Some people have no idea why a pharmacist, who is willing to sell those pills, would make that decision. The girls at Reality Check seem to fall into this group.  So Pharmer made an attempt to explain this to them, and added a bit of extra bonus information.

1) Many formerly over the counter remedies have been placed in restricted access due to abuse.  All cold remedies containing pseudoephedrine are now behind the pharmacist’s counter, and sales are restricted,  because people like to use that chemical to produce methamphetamine.

2) The morning after pills are sometimes abused by males, who give them to females without their consent, sometimes as a chaser to “date rape” drugs.  Because of this, it makes sense to restrict the sale of the morning after pills to men.  Congratulations to the pharmacist who had enough sense to understand  this, and take a stand to protect women.

3)  It is misbranding to refer to a drug as “contraception” if it does not significantly stop or delay ovulation during or after the luteal peak (during the most fertile time of the month).  Part of its action is due to mechanisms operating after fertilization.   The morning after pills are properly classed as “hormonal birth control”, not “contraception”.

4) The morning after pills have shown MUCH less  effectiveness than was initially claimed.  It makes NO sense for a woman to change sexual behavior due to reliance on the morning after pills.  They reduce pregnancy rates by about 60 percent, or LESS.

5) In general, the effect of marketing ulipristal acetate, and levonorgestrel as morning-after-pills will be to stem the decline of the abortion rate.   The spectre of increasingly abysmal medical care, overlaid by ever increasing drug shortages has possibly  killed the mood for a lot of women, leading to a dip in abortion demand in the U.S.  Heavily marketing a poorer quality birth control option might be enough to keep the abortion businesses alive.  Levonorgestrel MAP was strongly associated with that effect in Anna Glasier’s Scottish studies.

Pharmer finds the morning after pills to be problematic on a number of levels, ranging from ethics to efficacy, and doesn’t dispense them at all.

Caution to People Who Rejoice over 2009 CDC Abortion Data

New CDC data shows bungled abortion reporting in 2009.

Everyone is all abuzz over the 5% reduction in abortions shown in the 2009 CDC data. Instead they should be digging a bit deeper to see if the data really represents reality. Some pro-lifers target the reporters who expected an increase in abortions due to the economy. It’s true that poverty for women rose in 2009 and continues to do so.

The CDC is only able to count reported abortions, and therefore the data is necessarily incomplete. State laws requiring abortion reporting to a central agency vary from non-existent to un-enforceable.

The opportunity to induce home abortions and have them completed at hospitals has increased. These events cannot be reported as abortions unless the mom admits to doing something illegal, or accuses someone else of doing something illegal to her. Internet commerce has made home abortion chemistry much more accessible than in the past. Therefore it is unlikely that any numbers reported by the CDC are available. More recently Ulipristal acetate (Ella) has become available with online prescribing, providing a newer home abortion option using accumulated doses.

It should be noted that even without the above consideration, the CDC data on surgical plus mifepristone abortion is not comprehensive.

So far the joyful articles reporting the CDC abortion data of 2009 did not mention the LIMITATIONS section of the report, part of which is quoted below. Note that the CDC only reports 65 -69% of the abortions which are reported by the Alan Guttmacher Institute. Read on:

“The findings in this report are subject to at least four limitations. First, because reporting requirements are established by the individual reporting areas (17), the collection of data varies, and CDC is unable to obtain the total number of abortions performed in the United States. During the period covered by this report, the total annual number of abortions recorded by CDC was 65%–69% of the number recorded by the Guttmacher Institute (12,59), which uses numerous active follow-up techniques to increase the completeness of the data obtained through its periodic national census of abortion providers (12). Although most reporting areas collect and send abortion data to CDC, this information is given to CDC voluntarily. Consequently, during 2000–2009, seven of the 52 reporting areas did not provide CDC data on a consistent annual basis, and for 2009, CDC did not obtain any information from California, Delaware, Maryland, or New Hampshire.***** In addition, whereas most of the reporting areas that send abortion data to CDC have laws requiring medical providers to submit a report for every abortion they perform to a central health agency, in New Jersey and the District of Columbia, medical providers submit this information voluntarily (16). As a result, the abortion numbers these areas report to CDC are incomplete.††††† Moreover, even in states that legally require medical providers to submit a report for all the abortions they perform, enforcement of this requirement varies (60). Consequently, several other reporting areas tend to provide CDC with incomplete numbers.”

http://www.homeabortion.info/index.html

The Reason for FDA Approval of Ella, Ulipristal Acetate is HERE

RU—Serious? Jennie McCormack, the Next “Roe”? Good Grief | LifeNews.com.

Jennie McCormack aborted her 5 month unborn baby using mifepristone and misoprostil which she purchased online.
She was charged for illegally obtaining those drugs, doing a home abortion, and violating the ban on abortions after 20 weeks. She is appealing her convictions with the 9th Circuit Court of Appeals.

The FDA approved Ella for use as a morning after pill in an effort to provide another avenue for procurement of drugs for home abortions. Ella, ulipristal acetate, is a chemical analog of RU-456, mifepristone, and, in sufficient doses, operates by the same mechanism. Ella can be obtained from an online pharmacy in Utah, and doing so would circumvent one of the laws which McCormack has broken in her home state of Idaho.

‘I can’t give you the morning-after pill… it’s against my religion’ – Local – Hartlepool Mail

‘I can’t give you the morning-after pill… it’s against my religion’ – Local – Hartlepool Mail.

Another conscientious Boots Pharmacist acts up.   A 29 year old female patient, who desired to remain anonymous, was refused the morning after pill at a Boots pharmacy in Middleton Grange Shopping Centre, Hartlepool, UK.

She left the pharmacy in a state of shock, and was apparently  not able to get her pills until two days later.

Boots pharmacies has dealt with this issue before, and their spokesman acknowledges that the employees have a right to exercise conscientious objection, in refusing to dispense certain drugs.

The above linked article fails to recognize the manufacturer’s  stated multiple mechanisms of the morning after pills, and dishonestly states only  that they operate  to “stop the ovaries from releasing eggs”.

 

HIV testing at the DMV and Abortion drugs at the Discount Store.

D.C. brings HIV testing to the crowd at the DMV.

Washington DC, the HIV capital of the United states wants everyone to know that HIV testing is just a routine thing… conveniently available at the Dept of Motor Vehicles.  You can get an HIV test with your license renewal.

The FDA wanted people to be able to obtain abortion drugs, (ulipristal acetate, ELLA) an analog of RU486, mifepristone, at the discount store pharmacy.

Wouldn’t want people to drive out of their way to address these mattters.

In some states  Washington, for example, a student can be driven after school for an abortion, by a school official.  No parental consent or signature is needed for that extra curricular activity.

The highest value of our governments-gone-wrong is convenience

FDA remembers the old days, when it used to do its job.

Dr. Gerard M. Nadal appropriately nails the non-functional FDA to the wall, noting it’s new Kelsey award, honoring a former FDA reviewer from back when the agency was worth something.

Frances O. Kelsey, now 96 years old, is the namesake and first recipient of the Kelsey award from the FDA for doing what she was supposed to do. She stopped distribution of Thalidomide, for morning sickness, in the USA, likely sparing countless kids the associated birth defect called phocomelia, severely shortened limbs.

Nadal notes that the present FDA commissioner, Margaret Hamburg has ushered in the new drug Ella, ulipristal acetate, without appropriate testing, and with next to zero study of its effects on the babies who survive its embryocidal effects. In addition, the FDA has misbranded this drug as a contraceptive, thus disrespecting female patients’ right of informed consent to treatment.