Psycho-Babble Medication Thread 1027311

Shown: posts 12 to 36 of 75. Go back in thread:

 

Re: Hospital when feeling ok??

Posted by jono_in_adelaide on October 2, 2012, at 17:59:29

In reply to Hospital when feeling ok??, posted by b2chica on October 2, 2012, at 12:11:18

Agree with Phillips, sounds like you're entering a manic phase, either go into hopsital or start taking a sedating antipsychotic as an outpatietn (olanzapine?)

Be guided by your doctor -s/he is trying to help

 

Re: Hospital when feeling ok??

Posted by jono_in_adelaide on October 2, 2012, at 18:14:58

In reply to Re: Hospital when feeling ok??, posted by jono_in_adelaide on October 2, 2012, at 17:59:29

Oh, I just read that you're already taking olanzapine - guess that option is rulled out.

Go into hospital for a few days, get this under control, rather than let it turn into a train wreck.

If you arnt taking a mood stabaliser, definatly ask (demand?) that you start one

 

Re: Hospital when feeling ok?? » b2chica

Posted by phidippus on October 2, 2012, at 18:51:02

In reply to Hospital when feeling ok??, posted by b2chica on October 2, 2012, at 12:11:18

You're out of control. A hospitalization will help you stabilize.

Please go.

Eric

 

Re: Hospital when feeling ok??

Posted by Beckett on October 2, 2012, at 19:33:00

In reply to Re: Hospital when feeling ok?? » b2chica, posted by phidippus on October 2, 2012, at 18:51:02

>i am in need of something. some intervention but i dont know what i expect out of my doctor.

Yes, I hear you on this. It's difficult to trust someone when the stakes are high.

I think you need the intervention, too. Please work with your doctor.

 

Re: Hospital when feeling ok??

Posted by vbs on October 2, 2012, at 19:36:18

In reply to Re: Hospital when feeling ok??, posted by jono_in_adelaide on October 2, 2012, at 18:14:58

Based on your posts, I would say follow your pdoc's advice. You said that at one point you were feeling impulsively suicidal. And to top it off you're drinking and taking pills - not a good combination.

 

Re: PS. what should i do?

Posted by Zyprexa on October 2, 2012, at 19:55:58

In reply to Re: PS. what should i do? » b2chica, posted by SLS on October 2, 2012, at 14:16:27

> > i'm going home to take an early zyprexa. maybe i should try upping this generic brand to 10 and see what happens?
>
>
> Bingo.
>
>
> - Scott

ya thats what I think too.

All the money on hospital could buy a lot of zyprexa! But first try a bigger dose of generic.

 

Re: PS. what should i do? » SLS

Posted by phidippus on October 2, 2012, at 20:01:14

In reply to Re: PS. what should i do? » b2chica, posted by SLS on October 2, 2012, at 14:16:27

She needs a mood stabilizer.

Eric

 

Re: PS. what should i do? » b2chica

Posted by Zyprexa on October 2, 2012, at 20:09:41

In reply to Re: PS. what should i do? » SLS, posted by b2chica on October 2, 2012, at 15:17:54

Better yet you could take 20mg olanzapine and lots of perphenazine, get a lot of rest and don't drink too much tonight. I took very high doses of zyprexa when I was getting off the abilify and was very unstable for years. The high zyprexa did help. Now I only need 10mg olanzapine and thinking of stoping the perphenazine. Which also helped out when I was realy unstable. You might just have to put up with weight gain for a while, like I did, but now I'm losing it all. I'm back down to 195 lbs now, was at 230.

 

Re: PS. what should i do?

Posted by jono_in_adelaide on October 2, 2012, at 20:58:32

In reply to Re: PS. what should i do? » b2chica, posted by Zyprexa on October 2, 2012, at 20:09:41

B2, I take it your diagnosis is bipolar?

Are you not taking a mood stabaliser, and if not, is there a reason why?

 

Re: PS. what should i do?

Posted by phillipa on October 2, 2012, at 21:40:24

In reply to Re: PS. what should i do?, posted by jono_in_adelaide on October 2, 2012, at 20:58:32

Jono I think B2chica said she didn't do well on mood stabalizers. But B2chica you are playing with dynamite as you stated and remember you have to little girls whom you love who need a well Mommy. Phillipa

 

Re: PS. what should i do? » phidippus

Posted by SLS on October 2, 2012, at 22:45:40

In reply to Re: PS. what should i do? » SLS, posted by phidippus on October 2, 2012, at 20:01:14

> She needs a mood stabilizer.
>
> Eric


Zyprexa makes for a great antimanic and antisuicide drug.


- Scott

 

Re: PS. what should i do?

Posted by SLS on October 2, 2012, at 22:48:03

In reply to Re: PS. what should i do? » phidippus, posted by SLS on October 2, 2012, at 22:45:40

> > She needs a mood stabilizer.
> >
> > Eric
>
>
> Zyprexa makes for a great antimanic and antisuicide drug.
>
>
> - Scott


It is good for emergencies.


- Scott

 

Re: PS. what should i do? » SLS

Posted by SLS on October 2, 2012, at 23:40:39

In reply to Re: PS. what should i do?, posted by SLS on October 2, 2012, at 22:48:03

> > > She needs a mood stabilizer.
> > >
> > > Eric
> >
> >
> > Zyprexa makes for a great antimanic and antisuicide drug.
> >
> >
> > - Scott
>
>
> It is good for emergencies.
>
>
> - Scott

A true mood stabilizer is capable of treating acute episodes of both mania and depression as well as acting as a prophylactic to prevent future relapses into either mood state. Lithium meets these conditions. Lamictal and Depakote do not.

And yes, Zyprexa is a mood-stabilizer. It fits the strict definition, and has been approved by the FDA as being such. And no, Lamictal is not a mood stabilizer by this definition. It has antidepressant effects, but is not a good drug to treat acute mania. It is only marginally effective as a prophylactic against mania. Depakote can treat acute mania and help prevent future relapses, but does not ordinarily treat depression, and can sometimes produce it.


- Scott

 

Re: PS. what should i do? » Zyprexa

Posted by b2chica on October 3, 2012, at 8:48:09

In reply to Re: PS. what should i do?, posted by Zyprexa on October 2, 2012, at 19:55:58

Thanks everyone for input.
i decided to take max (prescribed) meds last night.
plus i doubled olanzipine to 10mg.
slept most of evening, woke up had bowl of cereal and went back to bed. slept till 6:45 this morning.

i'm feeling kinda apathetic with energy if you can understand that.

my urge to leave work is very strong. but i was fine an hour ago. ready to work. now i just want to leave.
**********************
i just filled out my time card for last two weeks and it looks like a checkerboard with the squirts of time i took off here and there.

this Cant look good.

not sure where to go from here.
i'm gonna stay on 10. suprisingly this brand olanzapine doesnt seem to make me crave food at all??? but i have lots of anxiety too.

 

Re: PS. what should i do?

Posted by b2chica on October 3, 2012, at 8:51:09

In reply to Re: PS. what should i do?, posted by phillipa on October 2, 2012, at 21:40:24

philipa is right. the only mood stabilizer (if its really that) is gabapentin. everything else i've tried had intolerable side effects or actually MADE me cycle.

and zyprexa has always ALWAYS helped me in the past. only difference is this time im on generics.

i better get some work done. only been here an hour and half but i'm ready to leave already...ugh. long day ahead. i hope i can last.
i think i'll tell myself that if i leave work i have to go to the hospital program.

 

Re: PS. what should i do? » b2chica

Posted by SLS on October 3, 2012, at 9:56:02

In reply to Re: PS. what should i do? » Zyprexa, posted by b2chica on October 3, 2012, at 8:48:09

I'm glad that you made it through the night and that you made it to work. However, I really feel that you should see your doctor and work out a plan. I think he needs to see you face-to-face.

Would you lose your job were you to go inpatient for a few days or weeks?

You might need to change APs. However, before doing that, you might want to investigate using higher dosages of the generic olanzapine. It might be a matter of differences in absorption between the name brand Zyprexa and the generic olanzapine. I would consider going up to 15 - 20 mg/day. I had something similar happen with Lamictal and generic lamotrigine. I needed to take more of the generic in order to get the same antidepressant effect. The Mylan brand generic lamotrigine really sucked. I needed to raise the dosage from 200 mg/day to 500 mg/day, and the therapeutic effects were still inferior to Lamictal.

If the higher dosage of olanzapine make matters worse, I think you should discontinue it immediately.

If Zyprexa is not the right drug for you anymore, you can explore Seroquel, Safris, or Latuda. Some people like Geodon. I think it is an unpredictable drug, though. Geodon can either reduce anxiety or make it worse, depending on the person. For some people, Abilify reduces depression and anxiety at the same time. However, like Prozac, there is sometimes temporary startup side effects such as an increases in restlessness, anxiety, agitation, or insomnia. For me, these things disappeared within a week. As with other APs, if Abilify produces true akathisia, you might have to discontinue it.

I agree with others in that you have presented with a mental state and behaviors for which hospitalization would be well-advised. Sometimes, a stay of 2 - 3 days is sufficient. I am guessing that there are plenty of treatment strategies that you have not tried yet. They might want to place you on Risperdal.

I am sure that whatever you and your doctor agree on will work out for you.


- Scott

 

Re: PS. what should i do? » b2chica

Posted by phidippus on October 3, 2012, at 10:06:36

In reply to Re: PS. what should i do?, posted by b2chica on October 3, 2012, at 8:51:09

Have you tried Keppra or Zonegran?

What kind of side effects did you get from the mood stabilizers?

Eric

 

Re: PS. what should i do? » SLS

Posted by phidippus on October 3, 2012, at 10:17:10

In reply to Re: PS. what should i do? » SLS, posted by SLS on October 2, 2012, at 23:40:39

The Zyprexa Chronicles: Marketing Zyprexa As The New Mood Stabilizer For Bipolar Disorder And Downplaying Diabetes And Weight Gain Concerns

This is an extremely lengthy post, one that requires use of the extended entry below, as well as numerous links to various Eli Lilly internal documents. Eli Lilly and the FDA were contacted repeatedly to answer questions. Neither replied.

Since mid-December, when the New York Times broke the news around accusations of alleged off-label marketing and alleged downplaying of risks associated with diabetes, weight gain and cardiac issues potentially connected with the use of Eli Lilly's Zyprexa, most of the resulting press attention, on and off-line, has focused on the drug's use in schizophrenia and dementia. In the latter condition, there have been accusations that Lilly marketed to drug off-label. The company has denied the accusations.

Little attention, however, has been focused on how Lilly targeted Zyprexa for use in bipolar disorder and how the company sought to change the medical treatment paradigm of patients with bipolar disorder by aggressively pushing doctors to use the drug, an antipsychotic, in mild cases of bipolar disorder, as opposed to cases of full-blown mania, and to use it as a long-term mood stabilizer along the lines of Lithium. This is not a minor matter. By some estimates, 50 percent of Zyprexa's $4.3 billion in sales comes from people taking the drug for bipolar disorder. The drug's use among these patients also potentially affects more patients, as bipolar disorder is estimated to affect from about six million to twelve million Americans. Schizophrenia is estimated to affect between two million to three million Americans.

As the company sought to turn Zyprexa into the "number one neuroscience drug in history," its strategy rested squarely in how much of the market for treating bipolar disorder it could carve off for Zyprexa. To do that, they cast Zyprexa as a long-term "mood stabilzer" far in advance of an FDA approval that would permit such language. Along the way, the company downplayed known risks associated with the drug.

CHASING BIPOLAR FROM THE START, WEIGHT GAIN CONCERNS

According to internal Lilly documents I have reviewed (and which I will link to throughout this post), the company aimed to go after this market more than a year in advance of Zyprexa's initial approval for schizophrenia in October 1996. In a document (3.9 MB) entitled (sic) "Zyprex--A Major Step Toward A Health Care solution For Psychosis" and dated July 20, 1995, "mania" is detailed as a new indication for the drug that the company planned to pursue in 1996 with "many" principle investigators at work on clinical research on the drug's use in mania (see page 43 of the lengthy document).

At the time, patients with bipolar disorder were commonly treated with a mood stabilizer such as Lithium, which had been approved for short and long-term maintenance use in the disorder since the 1970s. In some cases, an anti-depressant such as Lilly's Prozac would be added. Patients who experienced full-blown psychosis and were hospitalized were sometimes given an antipsychotic such as Mellaril, but only for short periods of time until the patient's condition stabilized. Some patients with mild symptoms of agitation, insomnia and racing thoughts might be given a small prescription of, say, Mellaril and be directed to take it for a few days only until their symptoms were properly knocked down. Mellaril is a "typical" or first-generation antipsychotic. Doctors were concerned that longer-term use of first-generation antipsychotics would lead to tardive dyskinesia and extrapyramidal symptoms and that such risks were not worth running when psychosis in bipolar mania tends to be short-lived and transient as compared with psychosis in schizophrenia.

Zyprexa was dogged by concerns of weight gain as far back as 1996 and Lilly's response, as it would be in later years, was to downplay concerns of weight gain. On October 1, 1996, Zyprexa was approved by the FDA for use in schizophrenia. The week before, it had been approved in Europe. Gary Tollefson, a Lilly official on its ironically-named "Heavyweight Team," conducted a conference call that day with several reporters to announce "the good news of the Zyprexa story." One reporter asked about initial reports of weight gain in some patients. Tollefson downplayed the concern, saying it was reported with all antipsychotics and that the patients were sometimes so underweight that the weight gain could be seen "in the majority of patients as being part of therapeutic recovery rather than an adverse event."

GOING AFTER LITHIUM, CHANGING THE PARADIGM

In a document (3.5 MB) from 1997, in which the company sought to "tee-up critical issues for the next 3-year planning cycle," company officials note that Lithium, an inexpensive generic product, was still the market leader in treating bipolar disorder. The company goes on to identify bipolar disorder as its number one goal for "disease state prioritization."

"Zyprexa will be the world's number one neuroscience drug in history," the document, authored by Tollefson, states in outlining the company's "strategic intent" for the drug. The company projected sales of $700 million for the drug in 1997, its first full year in the marketplace.

The company forecast that in the second half of 1998, Zyprexa would generate "'Depakote-like' uptake as a mood stabilizer," and already had a vision for its long-term use in treating bipolar disorder.

Both Lithium and Depakote were commonly referred to as mood stabilzers and were used in patients long-term. In Lithium's case, patients could well be on the medication for a lifetime (Depakote had only been used in bipolar disorder since the early-1990s.)

"To be a leader in the bipolar market, Zyprexa will need to be viewed as [a] true mood stabilizer (emphasis Lilly's). A true mood stabilizer will work in acute manic episodes without inducing depression, acute bipolar depression without inducing mania, and protect the patient from future episodes of mania or depression (emphasis mine)."

To "change the bipolar treatment paradigm" was seen as a major opportunity by the company, one that had "huge potential for (sic) increase in sales/value to Zyprexa and Lilly," according to the 1997 document. Weight gain was identified as one weakness of the drug, as was its cost relative to Lithium and Depakote. Zyprexa, at the time, cost on the order of ten times as much as a comparable dosage of Lithium.

As part of its bipolar marketing plans for Zyprexa, the company "planned/needed" bipolar disorder screening at the 1998 National Depression Screening Day, an activity sometimes carried out by the National Alliance for Mental Illness, as well as public relations programs aimed at journalists and grassroots media. In addition, the company hoped for an "Erasing the Stigma" partnership with the Rotary Club. The company planned to submit the drug for an acute mania indication with the FDA in 1998, according to the document. In 1999, the company hoped to have a celebrity spokesman on board.

"Zyprexa is a profound corporate opportunity," the document states. The company forecast as much as $1.1 billion in sales to bipolar disorder patients by the end of 2000.

"HIGH BLOOD SUGARS"

But in 1999, unsettling reports began to come in from clinicians. In a November 12, 1999letter (second part of letter here) from Albert Marrero, a staff psychiatrist with the Ventura County Behavioral Health Department, to Lilly's medical director, "high blood sugars" were cited as a problem.

"We have had eight patients out of possibly thirty-five patients on Zyprexa show up with high blood sugars," Marrero's letter states. "Two patients had to be hospitalized due to out of control diabetes....We have certainly never seen this with Haldol, Navane, Risperdal and others to this extent." It is not clear whether the patients were being treated for schizophrenia or bipolar disorder.

The drug was approved for short-term use in acute bipolar mania on March 17, 2000. Eli Lilly was prepared to change the paradigm.

THE ZYPREXA BIPOLAR LAUNCH

In March 2000, Lilly began a massive roll out of the drug for bipolar disorder. In a document from that month, the company detailed numerous marketing activities aimed at psychiatrists, according to the company document. A satellite symposium had been scheduled for February 23. Entitled "Clinical Management of the Bipolar Spectrum for the New Millennium," the program featured thought leaders in psychiatry such as Paul Keck, a psychiatrist at the University of Cincinnati School of Medicine, and was targeted at 6,000 doctors at 1,000 facilities and would also include 8,000 treatment team members such as nurses and social workers.

In addition, plans called for 15 bipolar dinner meetings, staged as continuing medical education events, and entitled "Restoring Balance: Long-Term Mood Stabilization in the Bipolar Patient." (Emphasis mine.) Anywhere from 150 to 400 psychiatrists were expected for each dinner. Lilly sales reps would attend as well, according to the document.

At the time, Zyprexa was not approved for long-term use.

It is not clear if such an event amounted to off-label marketing of Zyprexa for long-term maintenance use in bipolar disorder. Off-label marketing rules are murky and the FDA has not responded to repeated requests to clarify the matter. Neither has Eli Lilly. In general, companies can only market drugs to physicians for approved use. But doctors, paid by a company to speak for their product, have much more leeway to make broad statements about a drug's use, on or off-label, than do company sales reps, for example.

The company also planned to distribute a one-page "sell sheet" to 30,000 psychiatrists (that would be almost every psychiatrist in the US) and 95,000 pharmacists. In addition, Lilly planned to hold 30 regional "psychosis/bipolar weekend symposia" between April and November of 2000. Lilly also planned several other direct-to-physician initiatives between January and June 2000. The campaign aimed to "capitalize on reintegration, evolve private psych message to include depression data, neutralize weight gain." It consisted of a program called "dawn of a new era in treating schizophrenia and bipolar disorder."

The company had no indication for Zyprexa's use in depression.

In addition, Lilly planned to blast fax 30,000 psychiatrists every other month for three years with "schizophrenia, bipolar, elderly and health econ data," according to the document.

2001: BIPOLAR MAINTENANCE, LILLY DOWNPLAYS DOCTORS CONCERNS

In an "Integrated Product Plan" from January 18, 2001, it is clear that the company was pursuing indications for bipolar maintenance in the European Union and the US, according to a company document. In a separate document, the Zyprexa product team identifies "the Bipolar patient: mania, maintenance, depression" as one of its "2001 priorities."

Zyprexa was not approved for either depression or maintenance use in bipolar disorder at the time. It is not clear if the product team's priority for bipolar disorder translated into activities by Lilly's sales force in regard to long-term use of the drug. Lilly did not return repeated requests for comment.

But there was other troubling news afoot concerning perceptions about Zyprexa's side effects.

In April 2001 survey, 100 percent of psychiatrists surveyed believed that there was link between Zyprexa and diabetes and hyperglycemia. In this document, it is stated that the perception existed because some doctors were more selectively assessing their patients for diabetes and hyperglycemia if they are on Zyprexa, and, also, because more of their patients were on Zyprexa.

In a May 31, 2001 email, a company official reports on an FDA symposium called "Evaluating a Safety Signal in the Postmarketing Period: Hyperglycemia and the Atypical Antipsychotic Drugs." The symposium was led by Judith Racoosin, an FDA official. During a question and anser session, an audience member asked, "Where is the FDA headed with atypicals and diabetes?" according to the email.

"No decisions have been made" was Racoosin's reply.

A YEAR OF JAPANESE LABEL CHANGES

Lilly knew that a reckoning would soon be at hand for Zyprexa and concerns about hyperglycemia, weight gain and diabetes connected with its use. On January 30, 2002, the company's medical liaison in Texas emailed company officials to let them know of ongoing developments in that state's mental health system. Shelethea Dunning, the medical liaison, noted that Texas officials were hatching plans to have patients going onto Zyprexa go through baseline monitoring for glucose and weight, and to be continually monitored for changes. She explained that it was important for the company to do another presentation to researchers in charge of the state's so-called Texas Medical Algorithm Project, a highly-influential set of guidelines which was often used around the country as a tool for psychiatrists and other doctors in determining what medication to give to what patient. Dunning noted that TMAP researchers "are viewed as national leaders in mental health."

It is not clear what actions Lilly subsequently took. The company was soon faced with an even more serious challenge from abroad.

On April 15, 2002, Lilly learned that Japanese health officials would require a labeling change in that country. The label, according to a Lilly document, would instruct doctors not to use Zyprexa in patients with diabetes or in patients with a history of diabetes. The warning would also indicate that there was an increase in blood glucose for patients taking the drug. "Strongly disagrees" is what Lilly's assessment was of the Japanese decision.

"This does not change the status of Zyprexa as a safe, effective and cost effective agent in the US market," the internal document also states.

Lilly did not return a request for comment to clarify how the drug could be viewed as connected with diabetes in Japan but not in the US. The FDA did not return a request to clarify the same point and did not return a request to reveal what response the FDA undertook in light of the Japanese label change.

Within two months, Lilly showed just how much it disagreed with Japanese health officials.

"DONNA" AND LILLY'S MOVE INTO THE PCP MARKET

In June 2002, Lilly rolled out a new sales initiative for Zyprexa. The initiative was dubbed the "Zyprexa Limitless Team" and would create a primary care sales force targeting family practitioners, internists and other primary care physicians (PCPs) in an effort to sell them on using Zyprexa to treat patients in their practice who presented complaining of mixed mood symptoms such as agitation, insomnia and depression. The symptoms are considered hallmarks of bipolar disorder type 2 and cyclothymia, lighter forms of the disorder which stop far short of the psychoses and hospitalizations that are specific to bipolar disorder type 1 (or classic manic-depression).

The move into the PCP market was part of Lilly's long-held plan to reshape how bipolar disorder was treated. An estimated 50 percent of mental health care in America is delivered by PCPs, most commonly for depression. Typically, PCPs almost always refer patients with schizophrenia and bipolar disorder, key markets for Zyprexa, to psychiatrists much as PCPs refer patients with heart problems to cardiologists.

"Just as Prozac revolutionized the treatment of depression in the late 80s and throughout the 90s, so too will Zyprexa forever change the way primary care physicians view and treat bp disorder," the company states in a resource guide for sales reps. The company estimated bipolar disorder's prevalence in the American population at 6 percent. At the time, the National Institute of Mental Health estimated that the prevalence was a bit over 1 percent.

"We can change their paradigm," the document states. To do so, the company turned to "Donna," a hypothetical patient. It's customary in pharmaceutical sales to talk with doctors about hypothetical patient profiles and for the salesperson to work to convince the doctor that their product is what the doctor should be using on patients who meet that profile.

Donna, "a single mom in her mid-30s," was not even close to being a classic manic-depressive. She came into her doctor's office "seeming somewhat ill at ease. Her chief complaint is, 'I feel so anxious and irritable lately.' Today, she says she's been sleeping more than usual," continues the sales guide, "and has trouble concentrating at work and at home."

In a separate document from the campaign, sales reps are instructed to present Donna in such a way as to "make sure the kind of patient we are talking about today, [is] not the psychotic patient or severely ill patient, but the complicated mood patient."

The answer to Donna's problem was to be treated with Zyprexa, starting at a 5 mg. daily dose, roughly equivalent to 3 mgs. of Risperdal. "If her symptoms persist after one week, it is important to increase the dose to 10 mg--and you can feel comfortable doing so with Zyprexa's safety profile."

In the Donna script, the only safety issues addressed are those of other drugs and how Zyprexa compares favorably. The document states that older antipsychotics cause extrapyramidal symptoms--a truism--and that Zyprexa doesn't. In addition, the document states that Risperdal caused heightened prolactin levels in patients, but that Zyprexa did not.

"You will be able to assure Donna that Zyprexa is safe and that it will help to relieve the symptoms she is struggling with," the sales script states.

Nowhere in this Donna script is hyperglycemia or potential risks of diabetes mentioned, despite the fact that such risks were well-known at the time. As mentioned above, only six weeks earlier, the Japanese government had found such risks worthy of a serious label change for the drug.

"I would like you to get a patient like Donna started today," the script continues. "I will be back in a week to follow up."

In an undated "hyperglycemia/diabetes sell sheet implementation" document, the company notes, "Our goal and focus is on creating a market with Donna. The competition wins if we are distracted into talking about diabetes."

Nowhere does this Donna script instruct sales reps to communicate with PCPs about weight gain concerns. But the concerns were so prevalent among psychiatrists that a report from Lilly focus groups in March 2002 reported that psychiatrists saw a "100 percent association" between Zyprexa and weight gain.

In an undated document from the PCP campaign, sales reps are instructed in how to handle "frequent areas of concern" that might be brought up by some doctors. Reps were instructed to handle questions of weight gain by pointing out that "Zyprexa may cause an increase in appetite that can lead to weight gain....You can suggest that patients drink diet soda instead of regular soda or cut back on the amount of carbohydrates they eat."

Sales reps, in the same document, were instructed to handle diabetes concerns by stating that rates were comparable among all atypical antipsychotics. Not everyone believed the claim, however.

On Setpember 5, 2002, Lilly recived a letter from James Turnbull, an official at Frontier Health in Kingsport, Tenn. He explained to Lilly that 10 percent of their patients taking Zyprexa see changes in glucose, trigylcerides and cholesterol, as he had pointed out to the company in an earlier letter. Turnbull was not pleased with the company's reply, which I have not seen. "It just confirms the theory that there are lies, damn lies and statistics," he wrote.

As I reported last week, in October 2002 a Lilly medical writer exchanged emails with several company officials trying to "hammer out" how the company would characterize glucose production that arose in recent clinical studies of Zyprexa in the long-term treatment of bipolar disorder. The company was preparing submissions to the FDA to have the drug approved for maintenance use in bipolar disorder.

"John [Saunders] is ok with this explanation BUT has reservations about including it, because it operates on the assumption that olz [shorthand for olanzapine, Zyprexa's generic name] automatically increases glucose," [medical writer] Campbell writes in the email. "This may be a true assumption, but do we want to present this this way? Does inclusion of this explanation open us up to questions on glucose that we'd rather not bring up?"

In 2001, Zyprexa sales were approximately $3.3 billion. For 2002, the company reported sales of $4 billion, a 21 percent increase over the previous year, according to IMS Health.

AVOID REFERRING TO ZYPREXA AS MOOD STABILIZER

Double-digit sales gains were met with consternation by Lilly. In a 2003 "Brand Council" document (5 MB), the company describes its frustrations. The document is marked "for strategy and evaluation purposes." It called for hitting $6 billion in sales by 2006.

"Zyprexa obtains 'foundation of treatment' in bipolar in the US," the document states, but "only vs. AP's," meaning only in comparison with other atypical antipsychotics but not against mood stabilizers such as Lithium and Depakote. The company felt "significant" sales gains were possible in a "short time."

Still, the document states that Lilly should "avoid referring to Zyprexa as a mood stabilizer." The company expected a new indication for bipolar maintenance in early 2004.

On January 14, 2004, the FDA approved Zyprexa for use in bipolar maintenance. The company's press release cast the approval thus:

"Zyprexa is the first treatment in nearly 30 years to be recognized by the FDA as a treatment for both acute mania and maintenance treatment in bipolar disorder."

The other treatment approved for maintenance use was Lithium

 

Re: PS. what should i do? » SLS

Posted by b2chica on October 3, 2012, at 11:16:49

In reply to Re: PS. what should i do? » b2chica, posted by SLS on October 3, 2012, at 9:56:02

i tried to make appt with pdoc but she madeit for the 26th of october...gee could you get any further away?
i can call again today and see if i can get in sooner.

i would not loose my job if i were to go in for even a few weeks.

i never thought of going higher in the generic. course last time with the teva brand i went up to 10 and got psychosis. so i need to be careful. i was fine first couple days (like today) no psychosis symptoms. but CRAZY anxiety, earlier apathy with energy, but now energy with energy. getting agitated. took gabapentin about 1/2 hour ago.
boss left for a few hours. give me time to myself.


-seroquel gave me severe cognitive blunting but i have never tried latuda or safris. Geodon, gave me psychosis. abilify gave severe anger and agitation to well, lets just say my T was a witness to it.
and risperdal did nothing. didnt help depression or agitation, i was on that for about only a month but pdoc said that was enough. i should have seen something.

anyway.

i feel like a hopeless cause lately. my sypmtoms seem so all over the place, but i think its my mind more.

can you see more specific things in me? thats why i like to post true emotions. sometimes i can track myself that way.

anyway.
i'm just debating the money issue right now.
i want to give myself one more week. trying this different generic zyprexa and see what happens. and see if i can get into pdoc sooner.

thanks Scott


 

Re: PS. what should i do? » b2chica

Posted by phidippus on October 3, 2012, at 11:56:47

In reply to Re: PS. what should i do? » Zyprexa, posted by b2chica on October 3, 2012, at 8:48:09

I think you should do 20 mg on the Olanzapine.

Eric

 

Re: PS. what should i do? » b2chica

Posted by phidippus on October 3, 2012, at 12:27:09

In reply to Re: PS. what should i do? » SLS, posted by b2chica on October 3, 2012, at 11:16:49

>with the teva brand i went up to 10 and got psychosis

Can you describe your psychosis?

>CRAZY anxiety, earlier apathy with energy

I know you can't tolerate mood stabilizers, but one would go a long way to relieving your symptoms.

>Geodon, gave me psychosis

Can you describe this psychosis?

>but i think its my mind more.

How do you mean?

>can you see more specific things in me?

I see you're struggling to keep everything under control. You are not a hopeless cause.

Up the olanzapine to 20 mg, you'll get get better control of your mixed state.

Eric

 

Re: PS. what should i do?

Posted by b2chica on October 3, 2012, at 12:46:47

In reply to Re: PS. what should i do? » b2chica, posted by phidippus on October 3, 2012, at 12:27:09

>describe psychosis?

with TEVA zyprexa at 10 after 2 or three days i became raging paranoia, had to leave work cuz "everyone was staring at me, whispering things, they were going to tell the director of dept about my illness and i was sure she is going to do what she can to fire me." i was getting visual illusions about every 15min or so (very freq.) i was getting messages from whom i can only guess was the dead to give to others.

>Geodon psychosis?
i became enraged and started going to the 'seady' side of town looking for a gun. was having constant visuals of myself putting the metal gun in my mouth (was tasting the metal), and othertimes to my head feeling the pressure of the explosion. i was sure that others wanted me dead as well. very angry but lots of energy. other visuals like bugs and such. but the self-injury/death visuals were the worst.

i'm feeling more stable right now for the time being. i took gabapentin about 10:30 so its about fully kicked in now. (i notice in 10 min lethargy but 2 hours before it seems to help mood).
but yesterday i did a full cycle in one day, anxiety in morning, agitation afternoon. by the time i got home it was all i could do to lay down and dream of death. i fell asleep about 6, woke up 8:30 help put kids to bed. had cereal and about 9 or 9:30 went to sleep again.

if i go a full cycle again today i will call pdoc and speak with him.
and if upping zyprexa doesnt help i'll do hospital next week.

im thinking logically right now so anyway, thats the plan as i see things now.

thanks Eric.

 

Re: PS. what should i do? » phidippus

Posted by b2chica on October 3, 2012, at 12:48:11

In reply to Re: PS. what should i do? » b2chica, posted by phidippus on October 3, 2012, at 10:06:36

> Have you tried Keppra or Zonegran?
>
> What kind of side effects did you get from the mood stabilizers?
>
> Eric


i have tried neither. i've heard those names here but no where else...are they an herbal supplement? or Rx'd?

 

Re: PS. what should i do? » b2chica

Posted by phidippus on October 3, 2012, at 13:04:01

In reply to Re: PS. what should i do? » phidippus, posted by b2chica on October 3, 2012, at 12:48:11

Keppra is an anticonvulsant that has been studied as a mood stabilizer. It has few side effects. A 3000 mg dose is usually good at stopping mania fast.

Zonegran is another anticonvulsant and it has a bunch of case studies studies showing it is effective at treating bipolar disorder.

I've used both-I really like Keppra.

Both drugs require a prescription.

Eric

 

Re: PS. what should i do? » b2chica

Posted by phidippus on October 3, 2012, at 13:33:34

In reply to Re: PS. what should i do?, posted by b2chica on October 3, 2012, at 12:46:47

I'm inclined to think that the dose of your medication was not high enough and you started having psychotic features because of it. This explanation is simpler than trying to figure out how the medication made you psychotic when its designed to treat psychosis. I'm wondering what would have been if you raised the TEVA Zyprexa up to 20 mg.

Same goes for the Geodon.

>the self-injury/death visuals were the worst.

I get those all the time.

>I could do to lay down and dream of death

You're not suicidal are you?

Maybe you need a stronger antipsychotic. Has your doctor ever discussed Clozapine with you?

Could you tell me everything you're on?

Eric


Go forward in thread:


Show another thread

URL of post in thread:


Psycho-Babble Medication | Extras | FAQ


[dr. bob] Dr. Bob is Robert Hsiung, MD, bob@dr-bob.org

Script revised: February 4, 2008
URL: http://www.dr-bob.org/cgi-bin/pb/mget.pl
Copyright 2006-17 Robert Hsiung.
Owned and operated by Dr. Bob LLC and not the University of Chicago.