Commonly Prescribed Drugs And Hospitals Are Killing And Harming The Elderly
March 29, 2012 by admin
Filed under News Stories
March 29, 2012
Natural News
By Tony Isaacs
“Stop taking pharmaceutical drugs – doctor’s order.” –KTRN
Prescription drugs and the combination of those drugs and other medications are taking a heavy toll on elderly Americans, leading to risky hospitalizations, mental decline and death. And some of those drugs are worse than others.
A study published last November in the New England Journal of Medicine found that blood thinners and diabetes drugs caused most of the emergency hospital visits for drug reactions among people over 65 years of age in the United States. According to the study, just four medications – used alone or in combination – were responsible for two-thirds of the emergency hospitalizations among older adults.
At the top of the list was the blood thinner wayfarin, also known as Coumadin, which accounted for 33 percent of emergency hospital visits. Insulin injections came in second on the list, accounting for 14 percent of the visits. Aspirin, clopidogrel and other antiplatelet drugs prescribed to prevent blood clotting were third with 13 percent and just behind them were oral hypoglycemic drugs for diabetes which were responsible for 11 percent of the visits.
Last July, another study reported in The Journal of the American Geriatrics Society found that over half the elderly were regularly prescribed dozens of painkillers, antihistamines and psychiatric medications called anticholinergics which lead to mental decline and death. Researchers found that those taking more than one anticholinergic drug scored lower on tests of cognitive function than those who were not using any such drugs, and that the death rate for the heavy users during the course of the study was 68 percent higher.
Click here for the full report.
One Lot of Coumadin Recalled Over Potency Fears
May 12, 2011 by admin
Filed under News Stories
May 12th, 2011
WalletPop.com
By: Linda Doell
Bristol-Myers Squibb recalled one lot of its blood thinner medicine Coumadin after tests showed the tablets could be more potent than the dosage, said the U.S. Food and Drug Administration (FDA).
Coumadin — also known as warfarin sodium — is prescribed to treat and prevent blood clots, and to lower the risk of heart attacks and strokes. However, too much of the active ingredient in the medication means there would be an increased risk of bleeding, the FDA said.
Consumers should talk to their doctors immediately if they experience any problems, including pain, swelling, headache and dizziness, unusual bruising, nosebleeds and bleeding from cuts that take a long time to stop.
Included in the recall is one lot of 1,000-count bottles of Coumadin Crystalline 5 mg tablets, lot number 9H49374A, with an expiration date of September 30, 2012. The bottles were distributed to pharmacies for further dispensing to consumers.
Bristol-Myers Squibb said the recall is precautionary and is based on the company’s testing of tablets from a returned bottle. The tests showed a single table was higher in potency than expected.
Consumers should continue taking the medicine but should contact their pharmacist to see if they have tablets from the recalled lot. If so, they should contact their doctors immediately.
For further information, consumers can call Bristol-Myers Squib at (866) 918-8739.
In February, Upsher-Smith Laboratories recalled a single lot of its Jantoven Warfarin Sodium USP 3 mg tablets because a bottle contained higher-strength (10 mg) tablets.
Click here for the full report from WalletPop.com
Statins May Cause Muscle Damage in Some Patients
July 8, 2009 by admin
Filed under News Stories
July 6, 2009
Forbes
Statins, medications widely used to lower cholesterol, may cause structural damage to the muscles of people experiencing muscle aches and weakness, a new study has found.
The damage may occur even when tests for a protein thought to signal injury are normal, and may persist even after statin use is halted, according to the study in the July 7 issue of the Canadian Medical Association Journal.
The researchers stressed that people not experiencing significant pain had no cause for alarm and should continue taking the medicine.
About 10 to 15 percent of people taking statins report myalgia, or minor muscle aches and weakness, according to the study authors. A smaller number have stronger, persistent pain, called myopathy.
In the study, researchers biopsied leg muscle tissue from 83 patients: 44 were taking statins and had serious and persistent muscle pain; 19 were taking statins and had no myopathy, and 20 had never taken statins or suffered myopathy.
Of the 44 with myopathy, 29 were still taking a statin at the time of the biopsy, while 15 had discontinued their use for at least three weeks.
Biopsies showed that 25 of the 44 with myopathy had muscle damage, defined as injury to 2 percent or more of the muscle fibers.
Yet only one patient showed elevated levels of creatine phosphokinase (CPK), an enzyme expressed inside skeletal muscle cells, said study co-author Dr. Richard Karas, director of preventive cardiology at Tufts Medical Center in Boston.
Elevated levels of CPK in the blood can mean the enzyme is leaking out of the muscle cells, indicating muscle damage.
“This paper is challenging the dogma that if the CPK level is low, it rules out the possibility of muscle damage,” Karas said. “You can have microscopic muscle damage and the level of CPK can still be normal.”
The researchers also found that most participants showed signs of muscle injury even after they’d stopped taking statins.
“Although in clinical practice, the majority of patients with muscle symptoms improve rapidly after cessation of therapy, our findings support that a subgroup of patients appears to be more susceptible to statin-associated myotoxicity, suffering persistent structural injury,” said senior study author Dr. Annette Draeger of the University of Bern, Switzerland.
A study presented in September at the American Physiological Society meeting found that statins may hinder the body’s ability to repair muscles. Muscle cells exposed to increasing doses of simvastatin (Zocor) showed less ability to multiply and, therefore, heal and regenerate.
Over the past decade, statins have become the best-selling drug in America, accounting for $14.5 billion in sales in 2008. The drugs, which work in the liver to prevent the formation of cholesterol, are used in the prevention of coronary artery disease.
In the new study, 41 percent of those experiencing myopathy were taking simvastatin (Zocor); 31 percent were taking pravastatin (Pravachol); 17 percent were taking atorvastatin (Lipitor); 7 percent were taking fluvastatin (Lescol), and 3 percent were taking rosuvastatin (Crestor).
The study participants were experiencing pain severe enough to interfere with daily tasks and exercise.
The authors note that the sample size was too small to determine if one drug was associated with increased complaints of muscle pain or damage.
American Heart Association spokesman Dr. Roger Blumenthal said studies such as this may help doctors learn why some people develop statin-related side effects while others don’t.
In the study, the researchers noted that expression of ryanodine receptor 3 was heightened in those with structural muscle damage, offering a clue to the genetic underpinnings for those who suffer statin-related side effects.
“It’s a very interesting study,” said Blumenthal, director of the Johns Hopkins Ciccarone Preventive Cardiology Center in Baltimore. “This whole issue of why about one in 50 people on statins gets recurrent or severe muscle pain is very frustrating for physicians.”
Known risk factors for muscle pain include old age, high doses of statins, exercising vigorously while on statins and certain medications, including warfarin (Coumadin), cancer drugs, oral medications for fungal disorders and certain antibiotics, which interfere with the removal of statins from the body.
In 2001, cerivastatin (Baycol) was withdrawn from the market because of a high incidence in rhabdomyolysis, a widespread breakdown of skeletal muscle tissue.






