Sharon W. Dunn v. John G. Yager, M.D.

CourtMississippi Supreme Court
DecidedJanuary 13, 2009
Docket2009-CA-00599-SCT
StatusPublished

This text of Sharon W. Dunn v. John G. Yager, M.D. (Sharon W. Dunn v. John G. Yager, M.D.) is published on Counsel Stack Legal Research, covering Mississippi Supreme Court primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Sharon W. Dunn v. John G. Yager, M.D., (Mich. 2009).

Opinion

IN THE SUPREME COURT OF MISSISSIPPI

NO. 2009-CA-00599-SCT

CONSOLIDATED WITH

NO. 2004-IA-01833-SCT

SHARON W. DUNN

v.

DR. JOHN G. YAGER, M.D.

DATE OF JUDGMENT: 01/13/2009 TRIAL JUDGE: HON. ROBERT P. KREBS COURT FROM WHICH APPEALED: JACKSON COUNTY CIRCUIT COURT ATTORNEYS FOR APPELLANT: GREGG LINDSEY SPYRIDON PHILIP GIPSON SMITH ATTORNEYS FOR APPELLEE: BRETT K. WILLIAMS KEVIN M. MELCHI RICHARD WILLIAM FRANKLIN NATURE OF THE CASE: CIVIL - MEDICAL MALPRACTICE DISPOSITION: AFFIRMED - 04/14/2011 MOTION FOR REHEARING FILED: MANDATE ISSUED:

EN BANC.

RANDOLPH, JUSTICE, FOR THE COURT:

¶1. Sharon W. Dunn claimed severe back and leg pain caused by a work-related forklift

accident. After obtaining no relief following sixteen months of treatment from other

physicians, Dunn was referred to John G. Yager, M.D., a board-certified neurologist

practicing in Mobile, Alabama, with the Neurology Center (“Center”). On May 10, 1995,

Dr. Yager prescribed Tegretol to Dunn, which she began taking on May 19, 1995. On June 13, 1995, Dunn experienced an adverse reaction, which rapidly worsened over the next two

days. Subsequently, she was diagnosed as having Stevens-Johnson Syndrome (“SJS”). As

a result of the SJS, Dunn is now blind, along with other physical problems.

¶2. In April 1996, Dunn filed suit in the Circuit Court of Jackson County, Mississippi,

against multiple defendants, including Dr. Yager. Following the dismissal of all other

defendants by virtue of settlement, bankruptcy, or summary judgment, Dr. Yager is the lone

remaining defendant. Dunn alleged that Dr. Yager had failed to procure her informed

consent by failing to warn of alleged material risks associated with Tegretol, including SJS,

and that he had breached the standard of care applicable to a neurologist prescribing Tegretol

for neuropathic pain by failing to warn Dunn that flu-like symptoms may indicate an adverse

reaction to the medication.

¶3. In 2006, this Court determined that Dr. Yager’s interlocutory appeal from the denial

of his “Motion to Dismiss for Lack of Personal Jurisdiction” had been “improvidently

granted.” In January 2009, following a twenty-day trial, the jury found in favor of Dr. Yager.

Following the circuit court’s denial of Dunn’s “Motion for Judgment Notwithstanding the

Verdict, Relief from Judgment and New Trial,” Dunn filed her direct appeal, to which Dr.

Yager filed a cross-appeal regarding the issue of personal-jurisdiction.

FACTS

¶4. On September 15, 1993, Dunn was involved in a forklift accident at her workplace,

Ingalls Shipyard (“Ingalls”)1 in Pascagoula, Mississippi, resulting in back and leg pain. On

1 Now, Northrop Grumman.

2 September 29, 1993, Dunn visited Dr. Frank Fondren, an orthopedic surgeon in Mobile,

Alabama. Over the following sixteen months, Dr. Fondren prescribed numerous medications

and treatment modalities for Dunn, ultimately concluding that he had nothing further to offer

her. Dr. Fondren then referred Dunn to his partner, Dr. Jim West, a spine treatment

specialist, who determined that Dunn would not benefit from surgery. Thereafter, Dr.

Fondren referred Dunn to Dr. Yager.

¶5. In March 1995, Dunn returned to Ingalls in a limited capacity, first, as a secretary,

then, at the fuel depot, filling vehicles. On April 19, 1995, Dunn had her first office visit

with Dr. Yager. Dr. Yager’s first impression was that “[s]he may have radiculopathy on the

right. I will check an EMG, NCV as apparently these have not been done. I will try to get

the results of previous MRI’s, etc. She may well need [a] CT myelogram depending upon

the findings.” No medication was prescribed to Dunn at this time.

¶6. On May 10, 1995, Dunn had her second office visit with Dr. Yager. By this time,

Dunn had stopped working due to pain in her back and down her right leg. After reviewing

results of Dunn’s EMG and NCV tests, Dr. Yager found only “minor abnormalities[,]” and

proposed the following treatment plan:

I will get a CT myelogram to better define the lesions, if present, in the back and look for surgical problems. However, I am not very optimistic about that. I will start her on Robaxin 500 mg b.i.d. and Tegretol 200 mg advanced after one week to t.i.d. to see if this will help break her pain cycle.

(Emphasis added.) According to Dunn, in prescribing Tegretol, Dr. Yager asked only if she

had any allergies, then instructed her on “[t]he name of the drug and how to take it, the hours

3 in which, how much per day, how many hours in between . . . .” Dunn maintained that Dr.

Yager had failed to disclose any of Tegretol’s risks or side effects.

¶7. Conversely, Dr. Yager testified that he had discussed potential side effects, including

blurred vision and likely, although “not absolutely certain,” a rash. According to Dr. Yager:

[t]ypically when I . . . prescribe a patient Tegretol, you tell them what it’s for, you tell them a few side effects you may have, you tell them they could have allergic reactions, and you tell them if anything happens bad, you need to call us, anything you don’t understand. Those are typical of any drug used.

(Emphasis added.) While Dr. Yager acknowledged that he did not specifically mention flu-

like symptoms, a sore throat, and/or mouth ulcers as possible side effects of a severe reaction

to Tegretol, he added that “[t]here is no way” to distinguish between the flu and an adverse

reaction.2 Dunn and Dr. Yager agreed that he also told her, “if you have any problems, call

me.”

¶8. Tegretol was manufactured by Ciba-Geigy.3 By 1995, Tegretol had been approved

by the FDA for the treatment of epileptic seizures, but not neuropathic pain. As such, Dr.

Yager’s prescription was off-label. Multiple expert witnesses testified that in 1995, an off-

label prescription of Tegretol for neuropathic pain was common.

¶9. On May 10, 1995, the Physician’s Desk Reference (“PDR”) product information

regarding Tegretol included the following:

WARNING

2 This is significant, because multiple expert witnesses testified that, after the symptoms of SJS begin to manifest, it cannot be stopped. According to Dr. Yager, the treatment of SJS is simply “supportive.” 3 Now, Novartis.

4 APLASTIC ANEMIA AND AGRANULOCYTOSIS HAVE BEEN REPORTED IN ASSOCIATION WITH THE USE OF TEGRETOL. . . . HOWEVER, THE OVERALL RISK OF THESE REACTIONS IN THE UNTREATED GENERAL POPULATION IS LOW, APPROXIMATELY SIX PATIENTS PER ONE MILLION POPULATION PER YEAR FOR AGRANULOCYTOSIS AND TWO PATIENTS PER ONE MILLION POPULATION PER YEAR FOR APLASTIC ANEMIA.

...

BECAUSE OF THE VERY LOW INCIDENCE OF AGRANULOCYTOSIS AND APLASTIC ANEMIA, THE VAST MAJORITY OF MINOR HEMATOLOGIC CHANGES OBSERVED IN MONITORING OF PATIENTS ON TEGRETOL ARE UNLIKELY TO SIGNAL THE OCCURRENCE OF EITHER ABNORMALITY. NONETHELESS, COMPLETE PRETREATMENT HEMATOLOGICAL TESTING SHOULD BE OBTAINED AS A BASELINE.[4 ]

WARNINGS Patients with a history of adverse hematologic reaction to any drug may be particularly at risk. Severe dermatologic reactions including . . . [SJS], have been reported with Tegretol. These reactions have been extremely rare.[5 ] However, a few fatalities have been reported.

4 This entire capitalized “WARNING” section is known as the “black-box warning.” Dr. Terry Millette, tendered and accepted as an expert in the field of neurology, testified that the potentially life-threatening blood conditions of aplastic anemia and agranulocytosis are unrelated to SJS.

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