July 2013 - Page 2

Latest Gardasil HPV Research Fact or Fiction

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Recently, all the major media reported that the HPV vaccine was working. By their reports, the research showed a 56% reduction in HPV rates for vaccinated girls aged 14-19.

Even a decidedly feminist blog jumped on the bandwagon:

Perhaps one of the only reports to question the validity of these findings comes from an oncology blog for nurses. Assessing the Overall Impact of the HPV Vaccine – well worth the read. Leslie Botha from Holy Hormones Journal adds additional points of contention worthy of consideration. What the rest of the media failed to recognize and repeatedly fails to recognize either by want or by ignorance is that press releases are not often factually correct; something we write about regularly for Gardasil (here, here) and other medications or research (here and here). If a news or media organization is to report on medical and scientific research, they must be prepared to read and critically evaluate the actual research. Otherwise, they ought to label these reports what they are – advertisements.  Here is my take on the latest HPV research.

Behind the PR: Understanding the Research

Every couple years the Centers for Disease Control (CDC) and the National Center for Health Statistics (NCHS) sponsor what are called NHANES studies (National Health and Nutrition Examination Studies). These are health questionnaires sent out to a few thousand individuals deemed to be a representative portion of the population. Depending on the topic of study there are also laboratory based tests and/or in person followups at mobile examination centers (MEC). The study bandied about by the press, was published in the Journal of Infectious Disease (JID) by Markowitz et al., 2013. It compared NHANES data collected from 2003-2006, the pre-vaccine era and from 2007-2010, the post-vaccine era. An earlier study, also published in JID, but authored by Dunn et al. 2011, looked at the NHANES data from 2003-2006 and served as the foundation for Markowitz’s pre-vaccine/post-vaccine HPV analysis.

Background: HPV Prevalence and the Reported Reduction

Even a cursory reading of the Markowitz report – the report on which the PR suggesting HPV success is based –  immediately reveals problems. A deeper dive that includes the earlier JID study, the foundational pre-vaccine data to which the post-vaccine data is compared, demonstrates a statistical sloppiness that is difficult to attribute to ignorance. Numbers are missing, incorrect and misleading.

At the most basic level the data presented about the HPV vaccine’s effectiveness in the reported and marketed extensively by every major and media company are overblown and just a little bit hinky.  While it is true that the researchers report a 56% reduction in HPV rates in girls ages 14-19, that represents only a modest decline in the combined HPV rates (11.5% to 5.1%) tested. What the PR did not mention:

  • Other age groups saw an increase in HPV rates between the pre-vaccine era and post-vaccine era, suggesting that not vaccinating may be better
  • To arrive at this reported 56% reduction for the 14-19 year olds, the researchers had to combine the prevalence rates for each HPV strain tested (not all girls tested positive for all strains), then weight the results and transform – normalize the data to account missing data points and reign in the confidence intervals. The pre-vaccine prevalence rate of 11.5% was arrived at by summing the prevalence rate for each vaccine strain (HPV 6 was 5.4%, HPV 11 was 1%, HPV 16 was 6% and HPV 18 was 1.8%), but we would only know this if we pulled the 2011 study from whence the 11.5% figure came. Markowitz et al. did not annotate this figure. Not all girls had all strains and only HPV 16 and 18 are considered oncogenetic – potentially cancer causing.  Without noting how the 11.5% figure was arrived at and which strains changed from pre- to post-vaccine era, there is no way to determine whether the reduction from 11.5% to 5.1% came from the oncogenic or non-oncogenic strains. Nor is there any way to tell if the prevalence of certain strains increased over time instead of decreased. What if the observed reduction from 11.5% to 5.2% was largely based on HPV 6 – which initiates no more than genital warts?
  • From the total sample of 1363 pre-vaccine era girls and 740 post-vaccine era girls considered, girls from both time periods who were not sexually active and had no record of HPV or vaccine data were included in the original analysis reported in the PR. There was no stratification by these variables in the 56% improvement rate reported.
  • In secondary analysis, when HPV status was evaluated, only a very small sample size of sexually active girls in this age group (111 in the pre-vaccine data and 239 from the post-vaccine data, 8 girls from the post-vaccine sample had no HPV records) were included. These stratified data show that the rate of HPV was lower in non-vaccinated girls at 38.6% compared to 50% in vaccinated girls. So much for the most basic measure of efficacy.
  • The ages of sexually active versus non-sexually active by vaccine status were not given and thus, there is no way to determine whether vaccinating younger, non-sexually active girls has any protective capacity years later when the actual risk for HPV presents.
  • The error rates for some of the reported statistics, hailed as supporting the vaccines were over 30% (how much over, we do not know). Regardless, a >30% error rate is not a acceptable.

Read and Evaluate the Primary Research

Unless and until we get accurate and unbiased data from a large sample, that can be evaluated and verified independently, there is no way to tell if the risks of adverse events associated with this vaccine are reasonable and outweighed by the benefits of preventing cancer. Currently, data collected from the Vaccine Adverse events registry (VAERS) indicates a serious adverse event rate 4.3 per 100,000 doses of Gardasil. (Serious adverse events are those that cause death or are life threatening, require hospitalization, cause persistent disability or incapacity and/or require medical treatment to prevent permanent impairment or damage). This is compared to a risk of cervical cancer of 7.9 per 100,000 and death from cervical cancer at 2.4 per 100,0000 cases in the US. Considering VAERS contains only 1-10% of the total adverse events, the probability increased adverse events is high, so determining the benefits and the efficacy of this vaccine are important.

Who to Trust?

The more the vaccine industry, the CDC, the FDA and other agencies continue to promote truly spurious studies as relevant and proof-positive that a particular vaccine or medication is safe and effective, credibility is lost.  Without an effective counterbalance to the specious claims made by industry, consumers are left fending for themselves. What is perhaps the most dangerous result of this constant barrage of medical marketing and PR is that individuals who may truly benefit from certain vaccines or medications will avoid taking them because of the loss of trust. For the time being, you must pull the research, read and evaluate the studies yourself.

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Gardasil Injured

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I am the mother of my precious little girl Alisa (pictured). Though she is not little anymore, she will always be my princess. Alisa grew up healthy, active, and happy. She enjoyed trying new things and being around others. She loved photography, fishing, bike riding, boating, hiking, martial arts, music (especially her violin), and all types of animals. In high school she enjoyed her photography in which she won awards for. She was a tattoo assistant for a Washington State award winning tattoo artist and was learning the trade. She was on the swim team and loved swimming. Being a concerned mother I was fearful for her getting cervical cancer. We were being bombarded with commercials and ads for this vaccine for girls to be one less. When they offered the vaccine to my daughter I said sure. They never went over side effects or problems, so I figured it was a safe one. That day is when our nightmare began.

August 14, 2007, the first vaccine shot ( lot # 0384U) – Alisa went home with her injection site itchy, swollen, red, and sore. She was not feeling well, like flu. I sent her to bed and she was home sick for a couple days. The doctors office said that was normal. I did notice she was complaining about sore joints and muscles in the months to follow and she was napping more with headaches. I just blamed it on growing pains.

November 14, 2007, second vaccine shot (lot # 0927U) – Alisa was not thrilled about having the shot again. She was so scared she was going to feel crummy again. Sure enough the injection site was itchy, sore, red and this time the area swelled up a large area. She went home and went to bed. She was out of school again down with flu like symptoms for days. Slowly she came out of her slump but was so sore throughout her body. Sore muscles and joints, complained of headaches. She was exhausted all the time. It was difficult for her to muster the strength to do things. She took to her computer and was playing games online with friends.

Happy Valentines Day to you….February 14, 2008 (lot# 12APR10). This time she was flat terrified and cried all the way to the doctors begging me not to make her get the vaccine. This breaks my heart because I remember this day too vividly. I kept telling her it was the last shot and we don’t want to make the other two shots go without the final one. I kept telling her it was for the best. We left the office and she was throwing up, shaking, feverish, and the usual symptoms of sore muscles and joints, a pounding headache, exhaustion. She was down for over a week recouping from the shot.

After the 3 shots I put the series out of my mind. The only time that I remember the shots was EVERY visit to the hospitals and Dr.s offices, when they would ask if Alisa had all her vaccines. EVERY time I answered I said, “yes she has even had the Gardasil series.” Not one doctor put this together. The cause to her illnesses were put together by good friends of the family.

Many of you may wonder why I continued taking her in for the vaccine series.  I called the doctor’s office about her reactions each time, and they said it was completely normal to have those “minor” reactions: swelling, itching, light headed, and dizzy. After all it is a shot!!!! They also said at the doctor’s office, NO ONE has ever had the flu like symptoms from the vaccine, so she must have a touch of the flu. When the third dose came around they stressed to us that the other two shots of the vaccine would have been useless without the third. I trusted our family doctor of 15 years. He had never steered us wrong and always took care of us – treated us honestly and fair. I grew up with my grandfather being a doctor and most of my aunts being RN’s, I worked in the medical community. I trusted them….It never dawned on me they could be wrong.

Alisa continued on with her life but lost some of her spunkiness. She no longer had tons of energy. She slept a bunch, stopped her swim team, and spent more time in her room on the computer. She said her body hurt and didn’t feel like doing anything.

There are so many doctors appointments and hospital visits in this time frame. I have requested all her records from the hospitals, clinics, and her primary care provider (he has discharged her from his office).

October 2009, another visit to the emergency department with eye problems. She was having bloody discharge and pressure behind her right eye. Alisa was having problems with slurred speech,  headache and facial droop. They accounted it to pink eye and we begin treatment. They recommend we contact a neurologist and see the doctor.

After seeing the neurologist finally we were sent home with the idea of further testing later. Later that night the neurologist called recommending we take her back to the hospital for further testing. October 2009, off to the hospital again. By this time, Alisa was admitted into children’s hospital with the following symptoms: Bells Palsy, migraine, right sided weakness, blurry vision, tinnitus, balance problems,  numbness right side, unable to walk, problems swallowing, fatigue, joint pain, difficulty in opening mouth. They were testing for stroke and other unknown causes to this problem. She endured CAT scans, MRI’s, Lumbar punches. Over the next week she continued to get worse. Of course the psychiatric doctors were sent in to ensure she wasn’t an abuse victim. We didn’t know yet then she was abused by the pharmaceutical company. She was discharged without a cause to the problem.

This was Alisa’s senior year in high school, though the first semester she was in the hospital and a tutor came in a few times a week to drop off and pick up homework. The doctors released her to return to school but the noises, medications, and lights caused her headaches to pound and she was struggling with anxiety issues. With only one semester until graduation she dropped out of school. It was too much to handle. (She tested and passed her GED in Dec. 2011).

Over the following years Alisa has had this happen 2 more times. Right side paralysis, wheelchair, learn to walk with a walker again, and now she gets so exhausted she uses the wheelchair to save her energy.

Her side effects seem to increase in intensity and keep adding in numbers. So far she struggles with the following issues: leaky gut syndrome, pins and needles in extremities, dizziness, bleeding gums, toothaches/teeth changes, brain fog, sensitivity to chemicals, chest pains, constipation, dehydration,  enlarged liver, sound sensitivity w/anxiety, extreme pain in the tailbone area, fainting, fever and blisters, fibromyalgia, Guillain-Barre syndrome, autistic-like symptoms, hand/leg weakness, back pain, hot//cold intolerance, trouble sleeping, itching, joint pain,  knee pain, light sensitivity, blindness, depression, personality changes, anxiety/panic attacks, loss of bladder control, bladder issues, muscle aches and spasms, muscle tension, tumor, paleness, chronic fatigue syndrome, paralysis, pneumonia, severe nerve pain, shortness of breath, slurred speech, smell sensitivity, diarrhea, sore throat, stomach pain, swelling/edema, tremors hand and/or leg, random twitching of extremities, bloating, uterine spasms, hair loss, urinary tract infections (UTI), kidney issues, vision loss (temporary/permanent), vision  problems, dyslexia, hallucinations, vomiting blood, stomach ache, nausea, rashes, appetite loss, weight gain or loss ( 20-30lbs).

Alisa is unable to anything without supervision. Showering requires a shower chair. She has to be checked on constantly since her seizures come without notice. She becomes so disoriented after some of the seizures, she wanders off.

Alisa was once firm in her beliefs about anti-smoking and drug use, but has now become a medical marijuana patient. This is the only thing that takes an edge off the pain. She is never pain free but the MMJ makes it more tolerable. Unfortunately this pain relief isn’t covered by medical insurance so the $1200.00 a month pain control comes out of the pocket book.

This vaccine has dramatically changed our family’s life.  Alisa fights for her life everyday. It is even more difficult to not be able to help her or find a cure for her symptoms. It is heartbreaking to watch your child suffer in horrible pain and not be able to help. I feel guilty because my child is suffering because of a choice I made. A choice I thought was to help her and instead has disabled her. I wish someone would have told me. Please help spread the word about this vaccine. Tell everyone you know about the dangers of the vaccine. Educate before you vaccinate. This vaccine is harming thousands of girls, and now boys. The vaccine needs to be taken off the market. The numbers of children affected is rising everyday.

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Insensitive Remarks and Living with Chronic Pain

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Women with chronic pain, whether it’s due to endometriosis, an undiagnosed cause, or an autoimmune disorder, have heard it all before. I’ve found that people, no matter how well-intentioned, tend to give bad advice or say slightly hurtful things simply because they don’t know what you’re dealing with. Here are a few remarks I’ve heard more often than I’d like:

Well, you don’t look sick! While that’s somewhat nice to hear (nobody really wants to look sick), it dismisses the level of discomfort the person you care about may be in. I may look fine, but there’s some suffering going on here, and it would be nice if you didn’t wave it away. I may look fine, but I’m not going to be running a marathon anytime soon, so please be supportive.

You’ve lost so much weight! You look great! I’m not going to address the myriad gender and body issues that factor into this remark, but if you know someone has been ill for a long time, don’t mention their weight loss. They probably didn’t lose it in a healthy way. One of my friends would frequently be approached with this comment, followed by, “You could be a model now! How did you do it?” and she would respond, “Severe pancreatitis.” Please don’t embarrass yourself or the individual in question; it’s not your concern. Trust me, if I lost this weight in Crossfit, you would know by now.

You just want attention. No, that’s what support groups are for. If I’m letting you know about my chronic pain, it’s to explain why I can’t move those boxes, or attend your birthday party, or why I may want to stay seated today. I feel that friends and coworkers should know what I’m going through so I don’t look lazy, or they don’t get overly concerned when I suddenly have trouble walking or standing.

Ooh, I’d love some time off work. This remark, when directed at your mention of sick leave, is a real doozy. Please don’t confuse time taken off work for illness as a vacation. Unless you’ve lost a job to prolonged illness, you probably don’t know the sadness and stress of wanting to work and not being well enough to do so. Also, some women struggle with taking long weekends for illness, worry about losing their jobs, and must hope their bosses are understanding of their condition. As for me, I did not just take a seven month vacation; there were no margaritas and laughs at the pool. There were lots of meals eaten in bed and lots of Netflix, but if you factor in the multiple diagnostic procedures, surgeries, medications with disgusting side effects, blood tests and constant pain, it wouldn’t be a vacation you’d want to take.

With a better attitude/better diet, you’d get better in no time! This, I think, can be chalked up to wishful thinking. It sure would be nice if being a vegan and reading a ton of Deepak Chopra would make the pain and fatigue magically vanish, but it’s not going to happen that way. You can be sure that if someone is dealing with chronic pain and fatigue, they’ve consulted specialists about the proper diet, maybe going through several different diets. If it’s been going on for months, you can be sure they’ve read about emotional coping mechanisms or started therapy to deal with the depression and anxiety that often go hand in hand with chronic pain. Trying to shame someone into acting like they’re fine is pretty horrible, if you think about it. Some days will be better than others, but people are allowed to be down in the dumps occasionally.

Just suck it up, you’re not dying. People may not believe you, but you already are doing your best. If it takes all your strength just to make a sandwich and take a shower, and you just did make a sandwich and take a shower, then you are indeed sucking it up. I think people, especially caretakers, get frustrated watching someone experienced prolonged pain or discomfort that they can do nothing to change. This frustration with the illness itself may get projected onto you. Remember: You didn’t ask to get sick, and it’s not your fault. If you’re a caretaker and you find yourself getting angry, take a break, go for a walk, get out of the house for a bit, maybe consider a support group. Chronic pain is hard on everybody, not just the patient.

You’d feel better if you got out of the house/ got out of bed/ went running more. Yes, I’m sure I would, but this completely ignores the fact that I’m experiencing pain and fatigue. All I talk about and fantasize about is doing just that: going about daily life in a normal, active way. Sadly, my body won’t allow this, and that’s why I’m mostly housebound and mostly bedridden. When I do push myself and go against my better judgment, I end up being half-dragged, half-carried out of the supermarket to the car. Or, even worse, I faint in public, and it’s very humiliating. Don’t push someone to spend more energy than they have or ignore their pain; it will end in tears.

If people are less than supportive, you can suggest more helpful things to say. It takes guts, but you could say: “I’m letting you know that I’m in pain so you understand why I’m moving slowly today.” For friends or a partner: “I’m not feeling very well, and I’d like some support. Maybe we could plan an activity to do together when I’m feeling a bit better.”

I’ve learned that some people become downright hostile when confronted with spending time around someone who is in a lot of pain. Feel free to cut these people out of your life; they are afraid of illness because they fear experiencing it themselves and aren’t good at practicing empathy. Others don’t understand illness because they haven’t had friends or family live through it, and while they may be trying to help, they say insensitive things. Try not to let it get you down!

Why Hormones Matter

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I’ve been writing for Hormones Matter for several months now and I’ve been thinking a lot about just how much hormones really do matter. After all, we’re all only alive because of hormones when you get right down to it. Yet, most of us give very little thought to our hormones or why they matter until we’re forced to do so for some reason.

As young adolescents, we’re taught mostly in health class that hormones prompt our bodies to develop into those of men and women. We recognize that underarm and pubic hair growth is an indication that all is going well. Boys voices deepen and girls develop breasts. New sexual feelings slowly emerge and the world takes on new meaning and all things become more colorful. We become alive as it were and suddenly have another purpose – that of connecting sexually and of reproducing at some point. There’s a good amount of information about how hormones influence sex and reproduction. Sadly, the information seems to mostly end there. It wasn’t until my hormone-producing organs were removed through an unconsented hysterectomy and bilateral salpingo oophorectomy that I began to realize how much my hormones had mattered.

In simplest terms, hormones are chemical messengers which travel through our blood and enter cells, tissues and organs where they turn on switches to the genetic machinery that regulate everything from reproduction to emotions, overall health and well being. Certain hormones have an effect on particular cells known as ‘target cells’. A target cell reacts to a particular hormone because it bears receptors for that hormone. This is why there’s never a time in a woman’s life when she doesn’t need hormones. Hormones can be thought of as the life giving force that ‘animates’ us physically, mentally, emotionally and even spiritually. When a woman undergoes hysterectomy, hormone-producing organs are permanently removed and hormones are lost forever. It’s important to know that hormones aren’t only involved in the production of a new life (as in baby in the womb new life), they sustain all life.

Realizing How Much Hormones Matter

At the time of my father’s death from a massive heart attack in 2009, I was still reeling from hysterectomy and ovary removal in 2007. I’ll never forget the first time I saw my father’s body after he passed away. It hit me really hard to see him full of life one day and then see him completely and utterly lifeless the next. It hit my son Christopher even harder I think. I’ll never forget his comment as he looked at his grandfather’s ‘lifeless’ body just before the dreaded funeral. He said matter-of-fact like “Papaw’s spirit is gone. There’s no more animation.” Christopher’s observation was a very profound one indeed. In a very real sense, I suppose that is what death means – no more animation. I’d never thought of it exactly like that before.

Suddenly, I couldn’t help but think about how much I had changed since hysterectomy. It was as if the very life had been sucked right out of me too. I wasn’t dead, but I wasn’t really alive either – at least not in any way that mattered. Along with the loss of my female organs, I had lost my animation in many ways too. My eyes no longer sparkled. My skin no longer glowed. All things became dry, dull and lackluster. Everything became an effort and ‘feelings’ were no longer present. Remember how it felt when you became sexually aware? Well think of the opposite of that. While I once viewed the world in living color, things appeared mostly grey to me after hysterectomy and the loss of hormones. In short, I lost my animation.

Beyond reproduction and the other physiological functions ovarian hormones control, in many ways, these hormones animate us. They provide the subtle nuances that make life interesting – a life giving force that colors our physical, mental, emotional and even spiritual selves. To be animated is to have life, interest, spirit, motion and activity. What happens when a woman undergoes hysterectomy and castration? Pretty much the same thing that happens to a man who is castrated, she loses her animation, her color – everything that makes life interesting and worth living disappears. And this is on top of the health issues that arise from the loss of hormones.

There can be no question that hormones matter. It is too bad that we don’t know this until after they are gone. Please give this much thought before ever agreeing to removal of your hormone-producing and life-sustaining organs. Always weigh the benefits and risks.

Hysterectomy Research

Hormones Matter is conducting research on hysterectomy outcomes. If you have had a hysterectomy, please take a few minutes to complete The Hysterectomy Survey.

Advisory Panel Votes No, But FDA Approves Antidepressant for Hot Flashes Anyway

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OK, here we go again. Antidepressants are being touted as a treatment for menopausal hot flashes. This is nothing new because antidepressants have been prescribed for treatment of hot flashes for quite some time. A 2003 study reported in JAMA (Journal of the American Medical Association) showed a slight improvement in hot flashes for women using paroxetine (the active ingredient in antidepressants and the new hot flash treatment – Brisdelle) versus placebo. Other studies, show similar results and antidepressants for hot flashes have been prescribed off-label for about a decade. What’s new is that an antidepressant has now been ‘officially approved and recommended’ by the FDA.

So much about this FDA approval just didn’t set right with me. Perhaps, I am just tired of so many procedures, surgeries and drugs being recommended and approved for women, when in reality, most are not remotely helpful and can actually be quite harmful in the long run. So, I did some research and I uncovered a number of things that are very interesting, concerning and even somewhat alarming about Brisdelle and paroxetine.

What is Brisdelle?

Brisdelle is a selective serotonin reuptake inhibitor (SSRI) that contains the active ingredient paroxetine. Paroxetine is the SSRI used in common antidepressants such as Paxil, Aropax,Pexeva, Seroxat, Sereupin.

Side Effects of Paroxetine

The most common side effects associated with Brisdelle and other SSRIs include headache, fatigue and nausea or vomiting. As a paroxetine-based SSRI, Brisdelle may have side effects such as reduced sex drive and an elevated risk of osteoporotic fractures – both already risk factors for many menopausal women. Although the dosage of paroxetine in Brisdelle, approved for hot flashes, is lower than that typically prescribed for depression, the medication will still carry a black-box warning regarding paroxetine’s link to suicide (a known side-effect of paroxetine-based antidepressants is an increased risk of suicide). The black-box warning is the most serious warning that can be placed on the label of any prescription drug. Additional warnings will include an increased risk of bleeding and a risk of developing the rare, but increasingly more common adverse event ‘Serotonin Syndrome’. Serotonin Syndrome is a condition where there’s too much serotonin – leading to excessive nerve cell activity and causing a deadly collection of symptoms including confusion, changes in blood pressure, irregular heartbeat, seizures and unconsciousness.

Brisdelle Background

Noven Pharmaceuticals makes Brisdelle and funded the studies on the use of Brisdelle to treat hot flashes. Dr. James A. Simon, Clinical Professor of Obstetrics and Gynecology at the George Washington University School of Medicine in Washington DC, led the study. Dr. Simon openly reports having a financial relationship with Noven. The fact that Noven supported the study and provided the drug for the study, along with the fact that the lead doctor overseeing the study has financial ties with Noven, is troubling in my opinion, but standard fair in pharmaceutical research.

The FDA Approval of Brisdelle

The media is correctly reporting that the FDA approved Brisdelle. What seems to be missing from the headlines and discussion is the fact that the FDA’s advisory panel on reproductive health drugs voted against approval by a very large margin.  Indeed, the advisory panel voted 10 to 4 against Noven’s request for Paroxetine Mesylate, formulated as low-dose Mesylate salt of Paroxetine (7.5 mg/day), saying the drug’s minimal benefit didn’t outweigh its risks.

Panel members who voted against the drug pointed to the fact that women who experienced an average of 10 hot flashes per day experienced as few as 4 after 12 weeks of being on Brisdelle while women on the placebo went from having 10 a day to around 5. “I voted against recommending approval when I looked at the magnitude of the treatment effect relative to the magnitude of the placebo effect where there is no risk involved,” said Daniel L. Gillen, PhD, from the University of California, Irvine.

The FDA did not say why it ignored the advisory panel’s recommendation and approved the drug. Technically, it doesn’t have to follow the recommendation of its panel, but it is highly unusual that it didn’t in this case, since the vote was overwhelmingly negative. Where is the outrage? Where is the investigative reporting to determine why the FDA overrode its own advisory panel?

Why Approve Brisdelle?

What are we to make of this new drug that has been approved by the FDA for the treatment of menopausal hot flashes?  In my opinion, I don’t believe the FDA really needed to bother approving it because doctors routinely prescribe antidepressants off-label for women – for everything from heavy periods to insomnia and sometimes for no reason at all. Perhaps that is why they approved Brisdelle in the first place, it’s already being prescribed widely to women in this age group. A recent report suggests that 25% of women aged 44-59 are using antidepressants and overall there has been a 400% increase in antidepressant use from 2005-2008. Since women are already using antidepressants and there are currently no effective treatments for menopausal hot flashes, why not capitalize on this?  According to the New York Times:

Women “are begging for alternatives,” Dr. Andrew London, an obstetrician and gynecologist in the Baltimore area, told the committee, which met in Silver Spring, Md. If there were no approved drugs, he added, “They will get help on their own without us.”  

Brisdelle looks like just one more way to entice women to spend money on antidepressants and it could very well be dangerous.

The Dangers of Prescription Medications

According to Melody Petersen, author of “Our Daily Meds”, approximately 100,000 Americans die every year from their prescription drugs that they took just as the doctor directed. “This isn’t when a doctor or a pharmacist made a mistake or the patient accidentally took too much. This is when everything went right” she said.

My Take on Brisdelle and other Antidepressants for Hot Flashes

I am personally very leery of using paroxetine (no matter how small the dosage) to combat hot flashes. Simply stated, paroxetine is one of the most potent and selective of the SSRI-type drugs and the dangerous side-effects associated with it are well documented. With all of the evidence against Brisdelle or paroxetine and very little for it, I certainly don’t trust that it is a safe and effective treatment for menopausal hot flashes. Even if it has some small potential to help, I am not sure it would be worth the risks. I am very suspect of the FDA’s approval on this one. I don’t think I’ll be taking paroxetine anytime soon for any reason – least of all for relief of hot flashes.

Our Gendered Brains and the Bro-Code

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Attraction is complicated.

Imagine this scenario: You are at a bar, it’s late and the bar has all but cleared out.  You make conversation with several of the people that are left – some flirty banter ensues between you and the friend of someone whom you’ve been intimate with in the past. Inexplicable as it may seem you’re attracted to the friend – in this situation what do you do? Do you act on the attraction or ignore it due to moral conflict?

Chances are your answer will differ based on your gender. Society outlines a lot of ways in which we should act. Men have “Bro-code” or “Man-code” a set of rules, ranging from “no fanny packs” to “no sleeping with a ‘bro’s’ ex-girlfriend,” which define heterosexual inter-male bonding.

While the term “bro-code” might be new, its premise certainly isn’t. From a twenty-two year old friend, to my middle-aged father, to other various men I’ve interviewed – it is known that there are just some things that men shouldn’t do; with the most popular offense named as dating a male-friend’s girlfriend or ex-girlfriend. Of course, when asked further this rule only relates to male-male relationships (friends of ex-girlfriends or girlfriends are not off-limits).

Interestingly enough, women don’t ascribe to an unspoken code about dating. Yes, “girl-codes” (and the infamous “ho’s before bro’s”) have cropped up as a response to “bro-code” but generally speaking women have no defined ‘go-to’ dating code.

So why is it that men have an outline for their own appropriate moral behavior and women do not? Stereotypes and social rearing aside, the answer to this question likely lies in our neurobiology.

The first area of the brain which might offer hope in explaining the differences between male and female social thought processing is the temporal parietal junction (TPJ). The TPJ is the area of our brain most active during interpersonal emotional exchange, which seeks to find a quick solution during emotional discourses.  In men the TPJ is more active; suggesting that men seek to solve emotional quarrels faster than women do. Males also have much higher levels of testosterone which acts on their TPJ to decrease punishment concerns and make a more immediately pleasing decision in moments of social/moral discomfort.  Similarly the anterior cingulate cortex (ACC) also deals with social anxiety and a fear-of-punishment; in that it detects conflicts, weighs options, and motivates decisions.  The ACC is smaller in men than in women, which supports a woman’s likelihood to dwell and contemplate in emotional instances and a man’s likelihood to make quick decisions based on his TPJ.

Studies have shown that testosterone increases when in the presence of an physically attractive female. A spike in testosterone and TPJ involvement can explain why a man might ignore other emotional conflicts to pursue an attractive female. However, when in the presence of a female who is either related to a male friend or conjugal partner of a close male friend, a male’s testosterone levels have been found to decrease – thereby lowering the chance of acting on impulse and thus setting a foundation and a neurobiological basis for not dating a close relation of a male friend.

But perhaps the best neurological explanation for why men need a spoken social code and women do not is Mirror Neuron System (MNS), which allows for emotional empathy. The MNS allows us to detect the emotions of others by reading their facial expressions and interpreting their tone of voice and other nonverbal emotional cues. The MNS is larger and more active in the female brain – which may explain why women tend to “read into things” much more than men do.  While a male’s hormones and brain anatomy allows them to act first and think later – women’s brains are much more concerned with punishment and perception.  Whereas a large enough spike in testosterone might be all a man needs to do something he might regret later, a women likely has a whole arsenal of reasons (based on prior experiences, non-verbal cues and other interpretations) motivating her decisions.  In this sense it is hard for women to follow a simple moral code when so many factors can motivate their decision-making.

Of course studying attraction provides its own difficulties seeing as mate preferences are usually assessed when a participant is in a state of cool rationality. Yet, when truly attracted to someone (or after a night of drinking – as in our bar reference above) often a state of cool rationality does not exist – and for men, who are already looking for a quick way out of conflicting emotional scenario, perhaps a concrete rule is best for maintaining social stability.