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Archive for Drug Reactions

What is Virginia’s Statute of Limitations?

Wednesday, May 15th, 2013

     Who is Limitations and why is there a statute named that ? ice cream

     Yes, that’s probably the kind of question that I would have asked when I was a kid. For the same reason that I thought that the song  we were singing in church was, “Bringing in the sheeps… we shall Columbus, Georgia”,  instead of “Bringing in the Sheaves… We shall come rejoicing”.  That’s what happens when you sing what you hear, when you can’t yet read. Like Statute of Limitations, not statue of limitations.

     Of course, I really am doing a round about discussion of the question, “How long do I have to bring a lawsuit”? Well, below is a quick chart on some civil actions, provided from Lawyers.com.  Separately, ”When does the statute start to run” is a question that is sometimes argued to a Judge. 

      Still, even with the following chart, it still can be a bit confusing. kinda like:confusion chart 

Assault and Battery, 2 years

Va. Code § 8.01-243(A)

Contract (in writing), 5 years

Va. Code § 8.01-246(2)

Contract (oral or not in writing), 3 years

Va. Code § 8.01-246(4)

False Imprisonment, 2 years

Va. Code § 8.01-243(A)

Fraud, 2 years

Va. Code § 8.01-243(A)

Enforcing Court Judgments, 20 years

Va. Code § 8.01-251        

Legal Malpractice, 3 or 5 years (Depending on the type of contract or agreement)

Va. Code § 8.01-246(2) or (4)

Libel, 1 year

Va. Code § 8.01.247.1

Medical Malpractice, 2 and up to 10 years (Depending on the type of malpractice and when it’s “discovered”)    

Va. Code § 8.01-243(A) and (C)

Personal Injury, 2 years

Va. Code § 8.01-243(A)

Product Liability, 2 years

Va. Code § 8.01-243(A) and (B)

Property Damage, 5 years

Va. Code § 8.01-243(B)

Slander, 1 year

Va. Code § 8.01.247.1

Trespass, 5 years

Va. Code § 8.01-243(B)

Wrongful Death, 2 years

     So for pic o’ day, just in case you aren’t interested in a chart, how about a little lawsuit adversity that compares to… hand meets fist? I know… it’s getting crazy!

hand meet fist

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Illegal Sunscreen in School

Tuesday, June 26th, 2012

Violet and Zoe Michener came home from a field day at school with such severe sunburn, that their mother rushed them to the hospital. (NY Daily News).  The reason that teachers at the Tacoma, Washington school did not apply sunscreen? Because school policy forbids teachers from applying it to their students.

It’s one of those stories that usually gets somehow blamed on lawyers. Kinda like  peanuts at the steak house. People blamed lawyers when the peanuts disappeared, because of the lawsuits from slipping on the shells. Now, the peanuts are back because someone decided it would be a good idea to use buckets for the shells, instead of just having them thrown on the floor. Someone owns a thinking cap.

The sunburned sisters on the field trip, were in the sun for 5 hours without sunscreen. They even watched a teacher apply sunscreen “that was only for her”.  That morning, their mother didn’t apply sunscreen before they left, because it was raining.

School policy did not allow teachers to apply sunscreen for the students,  because it is classified as a medication. To use a medication, you have to have a prescription. It’s for liability reasons, they say. Now you can see the “shells on the floor” thinking.

The spokesman for the school system said that “because so many additives in lotions and sunscreens cause an allergic reaction in some children, we have to really monitor that”. So, instead of doing anything, the teachers watched as the girls just got burned. They even remarked at how red they were.

The ending to the story gets a little better because the state now allows school districts to implement their own policy regarding medication classification. In basketball, you can’t teach height. In life, I guess you can’t teach common sense.

For pic 0′ day, I went with the theme of being upside down, like the thinking on that field trip.

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Here Comes Qnexa

Sunday, February 26th, 2012

     One of my favorite commercials from the Super Bowl was the car commercial… What, you don’t remember a car commercial? Well, I’ll bet you’ll remember it when I describe it.

     A fat dog keeps seeing a car drive by that he wants to run outside and chase. The first time he tries, he can’t get through the opening in the door. So, he sits and looks at himself in the mirror to figure out what to do. He is sad. The violin music is playing.

                                                                                                                                                                          

     Off of a sudden, the voice of James Brown kicks in with, “Get Up Offa That Thing”. Heavy dog decides to go on a massive workout program to lose weight. He throws his ball down the steps, so he has to chase it. He runs on the treadmill. He ignores the food being dropped on the floor: He even goes out to the pool to swim.

   In thirty seconds, you feel a part of the accomplishment. Yes, he is through the door doggy hole and out chasing the VW Beetle. All because he decided to exercise and do it. He takes no shortcuts to weight loss.

  The New York Times did a story on the making of the ad, because so many people picked it as their favorite Super Bowl ad. YouTube even has “The Making of:The Dog Strikes Back” commercial.

     They decided to create a metaphor of “letting ourselves go” by showing Fat Dog. Originally, the director of the commercial was looking for two dogs. But, they decided that “Bolt”; the dog in the commercial, was such a good actor that they would just use special effects to accomplish the weight loss.

     Bolt wore a “fat suit” built out of fake fur. As the reporter of the Times put it, “No animals were harmed in the making of this fat suit”.

     We all can feel a bit challenged by this ad because it ends in accomplishment. Unfortunately, drug companies know that people aren’t inclined to exercise and would rather just take a pill to lose weight. They have been focusing on finding “that pill” and getting it approved for marketing.

      It’s why the diet drug, fen-phen, was so widely prescribed. Then, when it was shown to cause pulmonary hypertension and heart valve problems, the drug was taken off the market; and it led to damage lawsuit payouts of about $13 Billion dollars.

     Other drugs have failed to get approval. Even Qnexa was rejected in 2010. But, maybe enough time has gone by where the effects and dangers of fen-phen are fading from our minds.       

     Last week’s big pharmaceutical news is the potential arrival of  Qnexa to market. Vivus is the Mountain-View based drug company to create it. When the FDA gave tentative approval last week by a 20-2 vote, Vivus stock (VVUS) jumped 98 percent on its first day of trading.  At close on Friday, it is now trading at $22.13 and moved to $22.45 in after hours trading.

     I will briefly describe ingredients and warnings. No need for exercise with what they are touting.   

     In terms of weight loss, Qnexa’s study participants loss an average of 10 percent of their body weight. One analyst predicts that such results will make this drug “the next Lipitor” with millions of prescriptions being written.

     If you analyze the drug, you’ll find that it’s really a cocktail creation. It’s a combination of two previously approved FDA drugs. The first is phentermine, which is really an appetite suppressant. It was the “phen” of fen-phen.     The second part of Qnexa is topiramate, which is an anti-convulsant.  

     Phentermine is already known to have two heart-related side effects: tachycardia, which is an increased heart rate, plus it has been shown to elevate of blood pressure. It has been around for over 40 years.

     Topiramate is the active ingredient in Topamax. It’s side effects include confusion, memory loss, concentration problems and “difficulty in finding the right words” in conversation.

     It appears that the FDA is going to allow this to go to market, because of the positive effect in the war on obesity. The FDA  probably will require additional studies for those that are already at risk from the above two ingredients.

      Warnings probably will include cardiovascular issues. Plus, Topiramate already carries the warnings of depression, mood problems, fatigue and sleeplessness. Plus, there’s that side effect termed as “suicidal ideation”.

     The FDA will make a final determination on approval and required warnings on April 17. Vivus is asking the FDA to allow it to begin a 4-year-trial on cardiac health AFTER the FDA approves it. People will be excited with the weight loss and push to be on the drug longer. Then, history tells us that the drug company will push for a stronger version, for those that really need to lose weight.

     I suspect that you will be seeing more blogs from me on this drug, if it is approved. It would not surprise me, if this law firm becomes very familiar with this drug and drug company.

     For pic o’ day, I thought I’d post something that I think, describes this blog.

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Attitude at the Crash Scene

Tuesday, May 31st, 2011

     Guy Kawasaki wrote in “Reality Check“ about a friend  at O’ Hare  International Airport. He was watching another passenger scream at the airline attendant.  The ticket agent was amazingly calm.

     After the tirade was over, Kawasaki’s friend got up to the counter. He asked the agent how she was able to stay so calm. “That’s easy. He’s going to Paris, but his bags are going to Sydney”.

     Last week, we settled a case that involved a head-on crash between our client and the defendant. In the case, we had not gotten retained until sometime after much of the evidence, like skid marks and grass and gravel indentations, had disappeared or been washed away.

     There had been an eyewitness to the crash, who had told the police officer that the defendant had caused the crash, by traveling into the client’s lane. The police officer had written the name and phone number of the eyewitness on a piece of paper. Unfortunately, that paper disappeared. The officer regrettably advised  that he had failed to put the witness contact information in the investigation file, and that it had somehow blown out of his car.

     Now, we were dealing with a defendant who was saying that our client came into his lane, versus our client’s testimony of the exact opposite. (a “he said”, no “”he said”)  Because of hearsay evidence restrictions, the officer would be unable to testify about the statements of the eyewitness, at the scene. 

     At the scene, the defendant was extremely belligerent to the officer. He refused to do a field sobriety test. He claimed that he was in too much distress, to do a breathalyzer test, to determine alcohol in his system.    At the crash scene, he did have enough energy to measure skid marks. It was also later determined that after the crash, he called his sister; who is a registered nurse. Posssibly, he told her that he had been drinking and, maybe she gave him some advice on what to do at the scene. At least there was some possible inference that might have let the jury consider that as a possibility.

     Ultimately, the insurance company and defense attorney apparently thought that there was enough evidence, that a jury would believe our client. In fact, at the hospital, the defendant tested with  .03 of alcohol in his system. That’s almost 1/3 less than the legal intoxication limit of .08.  It does not appear that he was drunk  at the scene, after all.

     The defendant could have done the field sobriety tests and breath/alcohol test for the officer.  Instead, he was argumentative and not cooperative.

    I believe that it all came down to the attitude of the defendant. The way he acted at the scene, was also how he seemed, throughout the case. I’ll also venture a guess that the defense attorney was glad that he did not have to represent him in front of the jury.

     Like the airline passenger story, it’s a reminder how our attitude can make a difference. In this case, it also made a difference as to who was the most credible, as the cause of the crash.

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Bloomberg’s and AP Hormone Therapy Update

Friday, May 13th, 2011

The following is from a Bloomberg News and AP update on Hormone Therapy payments.  Our Firm is still in the middle of this litigation.  Pfizer purchased Wyeth about 2 years ago, which is why it is interchangeable in this article.

The AP (5 1/2, Johnson) reported that Pfizer “recorded charges totaling $472 Million as it reached agreements to settle about one-third of the lawsuits it faces” over whether hormone-replacement therapy (HRT) drugs made by its “Wyeth subsidiary caused breast cancer or other harm to women.”  In an  SEC filing “late Thursday, Pfizer said it took a $172 million charge in the first quarter to cover those agreements, plus verdicts in lawsuits it has lost.”  The pharmaceutical company also “recorded a $300 million charge in the quarter for the minimum expected costs to resolve all of the other outstanding hormone-replacement therapy actions against Pfizer and its affiliated companies.”

Bloomberg News (5/13, Feeley) reports that in February, Pfizer had “agreed to pay about $330 million to resolve 2,200 cases over the menopause drugs, according to people familiar with the accords.”  Overall, Pfizer’s “Wyeth and Upjohn units have lost eight of the fifteen Prempro [conjugated estrogens and medroxyprogesterone] cases decided by juries since trials began in 2006.”

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Akavar Class Action and Others

Monday, May 2nd, 2011

     It sounds like a great idea to be able to “Eat all you want and still lose weight”. Let’s put on our buffet pants right now. Unfortunately, you know the saying of “there’s no free lunch” . Now, we should also start saying that there is ” no all you can eat and don’t get fat lunch”. 

     A nationwide notice is being sent out, authorized by the United States District Court of Utah, relating to a class action lawsuit  that is being brought against the manufacturers of a weight loss supplement that is called Akavar 20/50.(Akavar) The lawsuit is called Miller v Basic Research LLC, et al. (Case No. 2:07-CV-871)

     In their ads for the supplement, the manufacturer made claims that the product had undergone “scientific evaluation” by a “team of doctors”.  The lawsuit alleges that there were no clinical trials; no scientific evidence that supported the claims of being able to eat anything you want and not gain weight; and that the advertisements were just making fraudulent claims.

          In 2009, Hydroxycut was recalled, because people claimed to have suffered severe liver damage injuries. I see their commercials again under the title of “Hydroxycut Advanced”. Now, they are pitching energy and weight loss in the same supplement. Notice, they hit the airwaves hard, right before swimsuit season. I wonder what change they made in the ingredients, that make it “Advanced”.

     Synerate weight loss was recalled, after more than 60 adverse events were reported. Many were deaths relating to heart attacks and strokes.

     The FDA just sent out a warning about an over the counter weight loss supplement called Fruta Planta. It is barred from the US and the warning went as far as to say that you should make sure that it gets thrown away, in a sealed container, so children and animals cannot  get to it.  

     It’s sad that people of bad character concoct some pill; set up a PO Box; and just start running TV ads that tout false claims. Meanwhile, people think that the ads are truthful and the pictures of the actors in their bathing suits, must be real. 

     The battle of the bulge lets these kinds of characters prey on the unsuspecting. History records that  Hitler believed that you should  ”make the lie big; make it simple; keep saying it and eventually they will believe it”.

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A Topamax Recall and Reminder

Thursday, April 14th, 2011

     “Something The Lord Made” is the HBO movie about controversial open heart surgery on an infant. At the time, it was extremely controversial to operate on the heart. Outside the United States, there had been some heart repairs as early as 1895.

     The movie discusses the religious opposition to open heart surgery at the time. There were some that allegedly believed that the soul resided in the heart and thus, should not be tampered with. Others believed that such medical conditions should be left to the determination of our Creator.

     I was reminded of this movie when I saw the recall for Topamax. Topamax is a medication that is prescribed primarily for epilepsy. According to the announcement by the manufacture, Ortho-McNeil Neurologics, the recall stems from four consumer complaints.

     The complaints resulted from an uncharacteristic odor in  pill bottles, that is thought to be TBA (tribromoanisole). TBA is a byproduct of a chemical preservative that is sometimes used on chemically treated wood. It could have gotten into a batch of Topamax, from wood pallets where the medication had been stored.

     Epilepsy  is one of the most common neurologic disorders. History tells us that it used to be sometimes known as the “Sacred Disease” because the resulting symptoms were believed to be a result of such things as demonic possession, or an attack by “other wordly” beings.  A 5th century treatise by Hippocrates discussed the attacks and their possible relationships to visions.

     Because the condition was not understood, some considered it to be contagious or poisonous. Treatments went as far to include literally drilling a hole in a person’s skull, to possibly attempt to either let the poison out or the evil spirit.

     This recall serves to remind us of how fortunate that we are with medical treatment and understanding today. Past medical conditions that were not understood, were given explanations that are obviously considered outrageous today. Maybe some of the treatments today, will also be deemed as an archaic to future medical care providers. 

     The other reason I blogged on this recall, is that it serves as a reminder to pay attention to our personal medications. A bad odor is cause for concern. Some may simply ignore their pill bottle when taking the medication. Also, medications are transported like other cargo and subject to issues beyond the manufacturing.

     In this instance, Ortho-McNeil is saying that the recall is related to fewer than 6000 bottles. Probably there’s a bit of a “conspiracy theory nut” in me, to always question the immediate discounting of any concern.

     I’m glad medicine has made such strides. I’ve been a benefactor of those advancements. Personal vigilence is also important and this recall is a reminder of that.

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The McDonnell Veto Part 2

Wednesday, April 13th, 2011

     Some blogs that I start, seem to have the initial excitement of an Amish Prom. I never fancy my blog to be hard hitting journalism and I try to stay generally away from the real politics.

     I am just  following up on Part 1  to give you some McDonnell facts to consider, as to why he would veto a House Bill that was overwhelmingly supported by republicans, democrats, the medical and insurance industry, and trial lawyers. I present…. you decide. Hmm, that almost sounds familiar. 

     I don’t expect this blog to cause hot taut tears, like the ones that Mr Bundchen had, coursing down his cheeks, when he was drafted by the Patriots in the 6th round of the NFL draft.(Tom Brady Crying) (OK, my anti- opinion is coming out here about Tom Brady and the Patriots… just can’t heppp it!) See what I’m doing here. A little bit of bias against Tom Brady, as an example of  what might have caused the Veto.

     The American Tort Reform Association  (ATRA)  says on their website that they formed because   “We are the only national organization dedicated exclusively to tort and liability reform through public education and the enactment of legislation.”

     ATRA states that they “identify and champion elected officials and judges who want to fix the system”.  Their intent is to “stop regulation through litigation”.  Their President of this national organization, Sherman Joyce, is a Virginia licensed attorney, so he is well aware of the laws going into effect in Virginia.

     For argument sake, let’s assume that these goals sound OK on the surface. Unfortunately, anything extreme can be dangerous. By “fixing the system”, what they have shown by their actions is to get matters away from juries because those crazy runaway juries can be influenced by “snake oil salesman” with law degrees.

     It’s no secret that business suffers when they have to answer to regulations. They can’t dump where they want to; they have to seek approval and sometimes get turned down on drugs and products to market; and they are held accountable for representations that are made. Take it out of a jury’s determination and limit accountability, helps make better quarterly profits.

     So why would this somehow be related to Governor McDonnell’s veto. Well, look at the goals of this organization. Then, notice where they have given money for campaign contributions. Why would they want to “champion” his candidacy? 

     In 2005, the American Tort Reform Association gave a donation of 200K into an organization called the Virginia Conservative Action Pac  (VPAC). VPAC then endorsed Bob McDonnell for Attorney General and …… donated 200K to his campaign. One of my previous blogs outlined additional ATRA contributions to McDonnell, so let me move on to another consideration.

     Eli Lilly manufactured and distributed a drug called Zyprexa. Its purpose was to treat depression and, specifically,  schizophrenia. Its warning label did not properly list the horrible side effects such as diabetes and other related death causing issues, that were then treated and paid for by many Medicaid programs in each state.

     Separately, Eli Lilly paid over 1.2 Billion to resolve individual claims. Then, state Attorney Generals brought action to get monies back from their Medicaid programs.  West Virginia, as one of the smaller states, received 22.5 million back in its coffers. Even Montana received 13 million.

     In Pennsylvania where they were based, Eli Lilly paid a fine of 1.42 Billion for fraud charges that were brought by Prosecutors there, because of the marketing and false labeling. Again, this was totally separate from any payout for the civil suits brought by over 30,000 people that were prescribed the drug.

     Let me try to get to my point quickly, because I think you know where I am headed.  32  states and  the District of Columbia were also paid 62 million for the reimbursement of medical bills that were paid by these states, from the Eli Lilly conduct. Now, google “Virginia and Eli Lilly settlement” or anything like that with ”Zyprexa” and see what comes up. (Waiting…Waiting) If you have clicked on the 62 million settlement and listing of states, you will also see Virginia not listed.

     In 2002, amid great fanfare, Governor Mark Warner announced 6 million of state money that was going to a new Eli Lilly plant in Prince William County.   In 2007, Eli Lilly stopped the expansion and operation and decided to go to Italy instead. No Warner parade over that one.

     What am I saying?  Our politicians usually are driven by money and their future plans. I’m suggesting that just as Bob McDonnell, as Attorney General, did not want to go after a pharmaceutical company for reimbursement to the state, he doesn’t want to be connected to any increase in a cap number; even when it makes sense for all sides and is agreed upon. This veto is a continuing trend.

     It took about 7 days to overturn his veto in the General Assembly. But,  he can now say that he voted against a cap increase. Plus, his past actions did not go after a Pharmaceutical company. By the way, look at the members of ATRA. Does it surprise you what I might suggest about the Big Pharma involvement?

     The mantra of politicians is that cap increases cost patients money; drive doctors from the state and drive up insurance costs. This comes straight from the politician campaign textbook. You’ll find others saying the exact wording.  However, you’ll never see statistics connected to that claim. Instead, connect the dots to campaign contributions for others that want to “champion” jury limitations and lack of Big Business accountability. 

     Someone is already probably getting his talking points together for his next campaign ad. He had to know that his veto was going to get overturned, didn’t he?

     I leave it to you to consider.     That’s just a taste of the trail of influence.  THE END.   I promise… No part 3

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No, Not a Raccoon Burger.

Wednesday, March 30th, 2011

     Join in with me and sing, “Frosted Lucky Charms, They’re Magically Delicious!”. Just kinda cheers you up.  Sure, maybe they have a bit of too much sugar in them,, but it was always fun to see if the marshmallows could outlast the boring cereal.
     Now we know the importance of the Food and Drug Administration (FDA). They have come out with an advisory (NY Times) about possible links between artificial food colorings, and behavioral problems, like hyperactivity in children. That means that products such as Jell-O, Lucky Charms and Minute Maid Lemonade, could be bad for kids.

     Because of the FDA, soon, products containing food coloring, will be required to carry warnings that such consumption can cause or aggravate behavior conditions in kids. Previously, the FDA had maintained that synthetic coloring that was added to these products, had no affect on children. Of course, manufacturers like General Mills are downplaying these recent studies.

     Because of the FDA, you might soon  see all Pop Tarts looking the same color and all Fruit Loops looking like “one Loop”. Or, they will have that scary warning on the side. Of course, maybe these food manufacturers are going to have some convincing product that “colors the food” safely. What, you thought the green marshmallows in the Lucky Charms were really from local leprechauns!!!!

     It’s a reminder of the importance of some regulation, and the importance of the FDA being properly staffed, to be able to render opinions on products that are on the market.

     If you looked at the title, you’re probably still wondering if this is a bait and switch title. What do Pop Tarts have to do with Raccoons? I promise, I’m not trying to drive you to eat a big bag of orange Cheetos.   

     I did open the eyes a bit, when I read a recent article in a SC newspaper. (GoUpstate.com) You just can’t sell whatever you want to, as an owner of a grocery store.

     South Carolina health officials have told a Richland County grocery store to stop selling raccoon meat. The Department of Health found bags of chilled racoon meat in a cooler at a Lucky Seven No. 2.  I guess that’s why you can’t buy greased beaver knees,  eye of newt or the lucky toe of frog, as recited by Shakespeare. They just aren’t approved. (well maybe the frog?)

     The racoon is an interesting animal to study. For the blog, I learned that a President owned one as a pet (named Rebecca) and that raccons have hands so nimble that they can unlace a shoe, unlatch a cage or retrieve coins from a shirt pocket. All those seem like talents that aren’t that helpful in the wild. Although, maybe that’s why I’ve never seen them in shoes. 

     Knowing that information about raccoons, makes me smile. Maybe an insurance company will soon have a raccoon as a mascot. On second thought, they do look more like the Hamburgler at McDonalds, with their little mask. They just shouldn’t be sold for meat in the grocery store cooler.

     You have to say “Amen to that!”. Ok, I know I’ve taken you on a long ride. Maybe you have to be nimble to find  a little bit of legal in here somewhere.

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Dollars For Docs Follow-Up

Sunday, January 9th, 2011

     In my previous blog, ”Drug Companies Paying Doctors“ , I cited a database called “”Dollars for Docs” that has attempted to compile  information on payments, that drug companies have made to doctors.

     It is not my opinion that just because a doctor receives compensation from a drug company, that it should mean that such payment means influence over that doctor.

     Unfortunately, there is not enough funding for doctors. Many times, the difficulty in even filling out the paperwork to try to receive research grants, can be overwhelming. Plus, many doctors, that I know, are already working long hours and fighting insurance companies to even get a portion of their entitled billing.

     I just thought that I would attach the website (here) which will allow you to plug in the name of any healthcare provider, to determine what monies that they might be receiving from the Pharmaceutical Industry.

     To me, it’s no different than lobbyists interacting with legislators on Capitol Hill. We know that industries contribute to campaigns. That doesn’t mean that every legislator is being “bought” by every contribution. 

     The reality is that medical treatment and research does cost money;  just like political campaigns cost money. I just think that it’s good to know who is paying and who is receiving.

     This website is not an exhaustive list. There are many doctors and payments still not listed. It is a good place to start. It goes along with the old saying that “information is the greatest commodity”.

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