Showing posts with label prescription medications. Show all posts
Showing posts with label prescription medications. Show all posts

Wednesday, April 27, 2011

7 Things Your Doctor Might Not Explain You

Visiting a doctor periodically for a check-up and getting tested alone does not prevent you from illnesses or risks. You have to get your medical examiner to be open and honest with you about the risks that you are facing if you do not commit to the said lifestyle changes, if there is a need for doing so.

7 Things Your Doctor Might Not Explain You

1. The Facts Behind 'Quit Smoking'

Any doctor is not going to be an alarmist and so the general advice would be to 'Quit smoking'. What he might not be telling you are the facts and the benefits behind quitting smoking. For instance, research has established that even a man who has been smoking for more than 20 years can reduce his risk of suffering a stroke hardly a year after quitting smoking. After a full year, your risk of suffering a heart attack will be equal to that of a non-smoker. It is up to you to decide if your health and your family’s happiness are as important to you as the 2.5 inches of nicotine rush or not.

2. The Truth Behind 'Exercise and Workout'

Typically whether you weigh the right amount for your age and height or not, your doctor is prone to advise you to 'Exercise and Work out'. If you are fit and exercise regularly, he is likely to ask you to keep it up. On the other hand, if you are overweight and do not exercise, he is going to insist that you start on an exercise regime immediately and keep pushing yourself just a little bit harder outside your comfort zone for best results. But what he might not tell you is that just three strenuous workouts a week are enough for you to show significant results in your overall health. But remember, not to exert yourself too much as it will have an adverse effect on your health.

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Wednesday, February 23, 2011

China Too Connected to IV Meds - Nursing Link

Walk into any hospital or clinic in China, especially in winter, and the crowds connected to IV drips swiftly confirm the worries of experts here that China is overdosing on IV meds, often for minor ailments.

Per capita consumption of antibiotics, commonly given by IV rather than the cheaper method of pills or injections, is 10 times the world average, said Wu Zhen, vice director of the State Food and Drug Administration, in December, the state-run Xinhua News Agency reported.

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Tuesday, February 22, 2011

Prescription Medications Take on Leading Role in Illegal Drug Trade - Nursing Link

Brian Freskos | Star-News, Wilmington, N.C.

February 22, 2011

Feb. 17—When Lt. J.A. LeBlanc arrived at the New Hanover County Vice and Narcotics Unit in 2001, one detective could handle the volume of prescription drug cases. Now, he said, all 16 detectives investigate them.

Street drugs such as cocaine and heroin have long been the targets of authorities seeking to root out illicit substances. But in recent years, growing prescription drug abuse has shifted law enforcement’s focus to stemming the flow of dangerous medications onto the black market.

Abuse of prescription medications, particularly narcotic pain relievers such as hydrocodone and oxycodone, is rising precipitously, leading White House drug czar Gil Kerlikowske last June to call it the “nation’s fastest-growing drug problem.” Between 1998 and 2008, treatment admissions for prescription pill addicts posted a 400 percent increase, according to the federal Substance Abuse and Mental Health Services Administration.

Southeastern North Carolina has not escaped what many law enforcement officials call an epidemic. Between 2004 and 2010, the New Hanover County Vice and Narcotics Unit seized nearly 15,100 pills — 3,749 of them in 2010 alone, the largest county pill haul in four years.

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Thursday, January 13, 2011

CMS 30-minute rule for drug administration needs revision, ISMP.org

In our June 17, 2010 newsletter, we covered a precarious topic best known as the “30-minute rule”—a requirement in the Centers for Medicare & Medicaid Services (CMS) Conditions of Participation Interpretive Guidelines to administer scheduled medications within 30 minutes before or after the scheduled time (see pages 174-175 at: www.cms.gov/manuals/Downloads/som107ap_a_hospitals.pdf). In our July 2010 nursing newsletter, Nurse Advise-ERR, we asked frontline nurses who are most directly affected by the 30-minute rule to weigh in on the issue by completing a short survey. And WOW, did they ever! More than 17,500 nurses responded to our survey, providing more than 8,000 additional comments (see Table 1 on page 2 of the PDF version of the newsletter), making it very clear that the issue is of great significance to nurses.

Respondent profile and compliance rates
Almost half of the responding nurses work on medical/surgical units, and the other half work in critical care, telemetry, or specialty inpatient units. Most nurses feel that the 30-minute rule is unsafe, unrealistic, impractical, and virtually impossible to follow. Approximately three out of four respondents (70%) told us their organization enforces such a policy. Of these nurses, only five of every 100 (5%) were always able to comply with the policy, while more than half (59%) were infrequently or only sometimes compliant (see Graph 1 on page 6 of the PDF version of the newsletter). Why nurses find it difficult to comply with the 30-minute rule was expressed by many (see Table 2 on page 3 of the PDF version of the newsletter), including a nurse who sent a pragmatic yet eloquent account of a Day in the Life of a Nurse (see Sidebar that follows this article). 

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Monday, January 3, 2011

New Drug Approvals Slipped in 2010 - WSJ.com

The Food and Drug Administration approved about 21 drugs in 2010, a relatively modest figure that shows the pharmaceutical industry hasn't yet escaped its drought in recent years.

A few potential blockbusters won approval during the year, but some of the most highly anticipated new products got delayed into next year or beyond. That partly reflects a tougher environment at the FDA, with regulators stepping up their scrutiny of safety issues in drugs for obesity, diabetes and other conditions.

According to monthly drug-approval reports on the FDA's website, 21 new drugs were approved in 2010, down from 25 in 2009 and 24 in 2008, but higher from a recent low of 18 in 2007.

The final approval figures, as well as the number of applications received by the agency in 2010, won't be available until next month. The approval figures don't include dozens of approvals granted for new formulations or new uses of existing drugs.

Although the 2010 figures are a bit lower than previous years, FDA spokeswoman Sandy Walsh said there's "no systemic change in how the FDA is approaching drug approvals."

The figures include several major biologic drugs, which are created from living cells and represent a growing portion of the pharmaceutical market. Amgen Inc. won approval for Prolia, a drug that is injected twice yearly to treat osteoporosis in postmenopausal women. Roche Holding AG's biotechnology unit, Genentech, won approval for Actemra, a drug that's administered intravenously to treat rheumatoid arthritis.

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Sunday, January 2, 2011

Drug recalls surge to more than 1,700 in 2009 - Aug. 16, 2010

Recalls of prescription and over the counter drugs are surging, raising questions about the quality of drug manufacturing in the United States.

The Food and Drug Administration reported more than 1,742 recalls last year, skyrocketing from 426 in 2008, according to the Gold Sheet, a trade publication on drug quality that analyzes FDA data.

One company, drug repackager Advantage Dose, accounted for more than 1,000 of those recalls. Even excluding Advantage Dose, which has shut down, recalls jumped 50% last year.

"We've seen a trend where the last four years are among the top five for the most number of drug recalls since we began tallying recalls in 1988," said Bowman Cox, managing editor of the Gold Sheet. "That's a meaningful development."

The fast pace of drug recalls seems to be continuing in 2010. Drug recalls totaled 296 from January through June of this year, said Cox. "If we continue at this same rate, we could get 600 or more recalls by the end of the year," he said. "That's still a very high rate of recalls."

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Saturday, December 18, 2010

How an antidepressant can hurt your patient, KevinMD.com

Patients still have shame about seeking help from a psychiatrist or other mental health professional. So they ask help for their depression from their primary care physician. The PCP feels an emotional pressure to provide the quick fix in that 15-minute appointment – the same pressure that he responds to when prescribing antibiotics to a adequately squeaky wheel of a patient with a common cold.

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Andrew Lopez, RN
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Thursday, November 18, 2010

Still on payroll despite fatal mistakes - Health News Florida

Of all the doctors in Florida that GlaxoSmithKline could have chosen as consultants, Steven Brooks and his partner E. “Jake” Jacobo would seem the least likely. They have a criminal record.

In 2001, the Orlando-area urologists pleaded guilty in U.S. District Court in Connecticut to one count of conspiracy to defraud Medicare and the military through a complicated black-market diversion of the pricey prostate cancer drug Lupron.

Despite the blotch on his record, Brooks is Florida’s third-biggest recipient of pharma speaking fees overall and commands by far the largest fees among those who have been disciplined, according to a data-mining  project by the investigative news site ProPublica. Working with the team there, Health News Florida analyzed the data for Florida and wrote a state-based analysis. 

Over the last 18 months, GlaskoSmithKline paid Brooks over $178,000, ProPublica found. The company also paid Jacobo $14,750.

Brooks

In the criminal case, federal prosecutors allowed the doctors to plead to a misdemeanor in return for repaying the government $1.1 million. They were sentenced to five years’ probation and 500 hours of community service.

According to an account in the Orlando Sentinel at the time, the doctors' attorney portrayed them as duples of pharmaceutical sales reps. He said it seemed like a business deal: The doctors bought extra supplies of Lupron in states where it was less expensive and arranged for resale in states where costs were higher, records said. This violated wholesale drug distribution laws.

The Florida Board of Medicine fined each doctor $10,000 and required them to take classes in medical ethics and risk management. Brooks gave up his medical license in New York, rather than fight charges stemming from the case.

Neither Brooks nor Jacobo returned calls from Health News Florida. A call to the drug company seeking information on the urologists’ roles as consultants and on whether the company knew about the federal case also went unanswered.

Who's running trials on new drugs?

Pharmaceutical companies depend on physicians to run clean clinical trials so they can get the data they need for Food and Drug Administration approval. Yet two drug-company consultants in Florida received FDA warning letters the over the way they ran clinical trials.

Last year, the FDA cited Francisco Hernandez of Hialeah for enrolling the wrong patients in a clinical trial of a diabetes injectable drug made by Sanofi-Aventis. Of 15 patients Hernandez enrolled, the letter said, 12 didn’t qualify.

The FDA also said Hernandez didn’t report illnesses in two of the patients that were serious enough to require hospitalization.

A similar letter went to Jeffrey R. Levenson in St. Petersburg for his work on the investigational drug Zyvox for Pharmacia and Upjohn in 2000, records show.

Levenson enrolled some subjects who were too sick to meet the outlines for the trial or even to give informed consent, the letter said. He also failed to report serious adverse events, it said.

Hernandez received $6,000 in the past year and a half from Lilly for consulting, records show. Levenson received $2,000 from GlaxoSmithKline and about $1,800 from Pfizer.

Neither returned calls from Health News Florida.

Experts on prescribing? Not so much

Doctors who are  paid speakers for drug companies are supposed to be experts in prescribing. According to records, though, several in Florida were anything but -- including psychiatrist Joseph John Altieri of Vero Beach.

(He is not to be confused with Dr. John Joseph Altieri, a Sarasota-based cardiologist)

Psychiatrist Altieri came before the Board of Medicine in 2008, charged with inappropriate prescribing to three patients.

In case documents, Department of Health investigators said Altieri provided a “constantly changing cocktail” of addictive drugs -- including potentially lethal narcotics such as oxycodone and morphine – to patients who Altieri knew or should have known were addicts.

The Board of Medicine found Altieri violated a slew of codes on physician conduct. He was fined $30,000 and placed on two years’ probation, with another physician supervising.

The DOH web site says Altieri recently completed his probation, but while it was still in force last year, he received $1,040 in speaking fees from Pfizer.

He did not return calls from Health News Florida.


Still on payroll, despite fatal mistake

Some doctors remain as speakers for drug companies, even after making very public, fatal mistakes.

Case in point: Tampa urologists Tod Fusia and Mark Swierzewski remain in demand as drug-company speakers even though they made a slip-up in surgery, killing a popular high-school teacher in October 2002,

The aim of the operation at St. Joseph’s Hospital was removal of a cancerous kidney. With Swierzewski assisting, Fusia used the then-new robotic arm to snip what he thought were the proper blood vessels. But they turned out to be the aorta and vena cava.

Despite efforts to stitch the vessels back together, the patient died the next day.

Their insurer settled the malpractice case for $1 million. The Florida Board of Medicine and Fusia settled the administrative charges with a $10,000 fine and 100 hours of community service.

Still, during the past 18 months, Fusia has received $6,500 in speaking fees from GlaxoSmithKline, according to ProPublica. Swierzewski got $4,175 from Lilly.

Neither of them returned calls from Health News Florida.

Not fatal, but still...

Another who bounced back from public humiliation is Dr. Charles C. Greene, an ear-nose-throat specialist in Jacksonville. In March 2002, when he set out to repair a patient’s blocked nasal passages by inserting tubes and instruments, he went too far.

An instrument penetrated the brain and removed part of the frontal lobe, according to Department of Health records. When the patient developed symptoms, Greene failed to act swiftly enough, the records said.

Other doctors eventually diagnosed a leak of brain fluid, blood clots in the brain and brain damage.

The family sued Greene and the parties reached a $500,000 settlement in April 2004. Greene also paid a $326,700 settlement in 2004 in a separate case.

In 2009 and 2010, GlaskoSmithKline paid Greene $16,600 in speaking fees, ProPublica found.

He did not return calls from Health News Florida.

--David Gulliver is an independent  journalist and founder of Sarasota Health News. Carol Gentry, Editor of Health News Florida, can be reached by e-mail or at 727-410-3266. 

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Monday, November 15, 2010

h2u.com : H2U : Health To You

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Uninsured Americans cannot afford many medications-KevinMD.com

I went to the doctor recently and got a new prescription.

The doctor was kind enough to give me some free samples, and a voucher that I could redeem to fill the prescription once at no cost. In the future, it will cost me $50 if I decide to refill it. If I didn’t have pharmaceutical benefits through my insurance coverage, the medication would set me back about $500 for a month’s supply. For those of you doing the math, yes, that’s $6,000 a year. Suffice it to say that I wouldn’t be filling the prescription. And that’s exactly what many Americans do.

For many low-income uninsured Americans, a number of important medications are out of reach because they are simply unaffordable. These are medications that treat chronic diseases like hypertension, high cholesterol, and other common illnesses. They are effective medications that can make a huge difference in a person’s quality of life–including whether or not they die an avoidable death. In a show of good faith, most pharmaceutical manufacturers provide access to no-cost or reduced-cost brand name medications (the ones they manufacture, of course) to this “gap” population. The trouble is, few people know about these programs, which offer tremendous assistance, but require people to jump through a number of application hoops to qualify for the cheap or, in some cases, free meds.

Dr. Heather Whitley has an article out in the latest issue of The Journal of Rural Health, which attempts to quantify the value of these prescription assistance programs (PAPs) at a clinic in Alabama. Head south from Tuscaloosa, and you’ll find yourself in Hale County–one of the 50 poorest counties in America with an average annual income of $14,927 per person. In Hale County, is a town called Moundville, and it is here that the Moundville Medical Clinic operates with a single physician, a nurse practitioner and a couple of nurses. This is one of those places that most Americans don’t know–or at least really don’t like to acknowledge–exists in the United States. If ever anyone needed help obtaining prescription medication, the patients of the Moundville Medical Clinic would be first in line.

The clinic has a pharmacist who works two days a week to help patients navigate the PAP application process. Costs are offset by charging patients $5 per completed and mailed application. In most cases, that is a small price to pay. Dr. Whitley looked at the data collected by the clinic to assess the value of the program–that is, how much free or reduced-cost medicine were patients getting?–and found that across a two-year period (2007 and 2008), the PAP program at the Moundville Medical Clinic brought in more than $138,000 in free medications.

That’s a lot, yes, but what is even more striking is when you consider that that was only for a total of 31 patients. In other words, each patient received about $4,500 in free medication on average during the study period. That’s a pretty remarkable benefit in return for filling out some complicated paperwork, and it suggests that — until real health reform and cost-control is achieved — clinics that see a number of PAP-eligible patients should strongly consider investing in such programs, even if it means having someone volunteer their time one day a week. The benefits far outweigh the costs, but there are administrative hurdles that must be cleared before the benefits can be accessed.

Brad Wright is a health policy doctoral student who blogs at Wright on Health.

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Thursday, September 23, 2010

RxDrugSAFE

RxDrugSAFE:"RxDrugSAFE is the newest weapon in the fight to prevent prescription drug abuse from toddlers to teens. RxDrugSAFE is a real steel safe that uses advanced, simple to use, fingerprint recognition to open. Only parents, guardians or other authorized users can program and open RxDrugSAFE. RxDrugSAFE is the most secure prescription medication safe for home use on the market. RxDrugSAFE is designed to be securely mounted in drawers, closets or cabinets, but can also be used when traveling as well."
info@rxdrugsafe.com
http://www.rxdrugsafe.com/

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Wednesday, September 1, 2010

WikiAnswers - Is diphenhydramine safe to take after expiration date

Wondering about that expiration date on your medicine bottle?

WikiAnswers - Is diphenhydramine safe to take after expiration date:"It turns out that the expiration date on a drug does stand for something, but probably not what you think it does. Since a law was passed in 1979, drug manufacturers are required to stamp an expiration date on their products. This is the date at which the manufacturer can still guarantee the full potency and safety of the drug."
http://wiki.answers.com/Q/Is_diphenhydramine_safe_to_take_after_expiration_date#

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