In the interest of fairness to one and all
Here is Eli Lilly’s statement in response to the New York Times article about a man who died. His mother alleges his weight gain—which she traces to Zyprexa—is what killed him. The company disagrees.
INDIANAPOLIS, Jan. 4 /PRNewswire-FirstCall/ — Eli Lilly and Company (NYSE:LLY) believes it is inaccurate to imply that any single factor — including medication — was the cause of the unfortunate death of the patient profiled in today’s New York Times.
Millions of patients around the world have benefited from Zyprexa and Lilly is concerned that this tragic story about a single patient could unnecessarily frighten people with schizophrenia and bipolar disorder and cause them to discontinue their medication without first consulting a physician. Furthermore, we are disappointed that the Times chose to focus its entire article on only one patient rather than speaking with additional patients and/or family members who have different views and experiences with Zyprexa. We encourage patients or caregivers with questions to consult their treating physicians or to call Lilly at 1-800-LILLY-RX.
Lilly released the following statement to the Times to ensure patients who take this medication have the information and reassurance they need.
“Lilly is saddened by the death of Mr. Kauffman and our deepest sympathy goes out to his family and friends. We were made aware of this patient’s death and reported it — as we do all adverse event reports we receive — to the FDA. It is well-understood that adverse event reports don’t signal causation — they only signal that the individual was taking a particular drug at the time of a health event.
“Though we do want to protect this patient’s privacy, we want to provide enough information to reassure the millions of patients who are taking this lifesaving medication. To that end, it is important to note that the adverse event report indicates that this patient had a complicated medical history that may have led to this unfortunate outcome.
“Numerous studies have demonstrated that people with severe mental illness, such as bipolar disorder, have significant co-morbid medical conditions, such as cardiovascular disease and diabetes, regardless of whether they take medication and regardless of which medication they may take. Other studies have found that the health burden of severe mental illness can reduce life expectancy by between 8-20 years when compared to the general population. Very often other risk factors like heavy smoking and drinking for example complicate the medical condition of patients suffering from severe mental illness.
“Patient safety is our first priority at Lilly. We take seriously and thoroughly examine all adverse event reports received through post-marketing surveillance (also known as spontaneous adverse event reporting), from both health care professionals and consumers. We follow up on reports diligently and intensely — as we did in this case. Although these reports are not publicly available, they are shared routinely with regulatory authorities. It is widely accepted that these reports do not address causality but they are important and can help guide further evaluation into potential safety signals. However, they cannot be interpreted in isolation from clinical trial data.
“Zyprexa was approved by the FDA in 1996 and remains on the market today. It has been the subject of nearly 100 studies over the past 23 years and has been used by more than 20 million people worldwide. Doctors continue to prescribe it to deal with some of the most terrible mental illnesses, such as schizophrenia and bipolar disorder. The FDA has looked at the entire body of evidence that Lilly has continued to provide over the years, and has affirmed the benefit that this medicine can give to patients when accompanied by appropriate labeling regarding benefits and risks.
“We remain confident in the safety and efficacy of Zyprexa based on the depth and breadth of scientific research conducted around the world. Zyprexa is a lifesaving drug and it has helped millions of people worldwide with schizophrenia and bipolar disorder regain control of their lives.”
liz | 6:36 PM | Uncategorized




Liz-
Appreciate your comments, and do agree with the challenge of meds with significant side effects, and the prevalenced and big problems associated with mis or unidentified “comorbid conditions.”
I jump up on my soap box when these problems stare us in the face for years [big metabolic problems in the office], and we stay in the denial groove because we don’t have “academic endorsement” -only- “anectodal information.”
Let’s think for a moment, do cigarettes cause lung cancer…. can you prove it??
You will love reading Michael Porter from Harvard Business on health care.
Thanks for the tips,
Chuck
Liz,
Regrettably, little or no coverage has been given to the role of prescribing physicians and psychiatrists. Zyprexa is a legend drug necessitating a script from a physician. I would have hoped that all doctors were duty bound to take notice of a consumer’s weight gain or an increase in his or her blood glucose level, consider its causes, and assist the consumer in addressing the issue.
Where no less than absolute medication compliance is expected, don’t consumers deserve medical care that takes into account this expectation?
I find it irresponsible and negligent on the part of the drug maker to not disclose all relevant information and to also lay all blame and responsibility at the doorsteps of the physicians.
The patient too has got to take responsibility.
Let us not forget what I believe is incumbent upon the patient to make sure to have regularly scheduled periodic examinations and even more so when ingesting medications and subscribing to various treatment regimens.
The patient should be educated not only by the physician but through one’s own readings. Laying blame doesn’t resolve the basic goal/issue of trying to obtain wellness.
If we ban all drugs and treatments we’ll be left with…Doesn’t anyone take any responsibility for their own actions any longer?
Warmly,
Herb
VNSdepression.com
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