Janssen Pharmaceutica, Inc. v. Bertha Grant

CourtMississippi Supreme Court
DecidedJanuary 10, 2003
Docket2003-IA-00174-SCT
StatusPublished

This text of Janssen Pharmaceutica, Inc. v. Bertha Grant (Janssen Pharmaceutica, Inc. v. Bertha Grant) 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
Janssen Pharmaceutica, Inc. v. Bertha Grant, (Mich. 2003).

Opinion

IN THE SUPREME COURT OF MISSISSIPPI

NO. 2003-IA-00174-SCT

JANSSEN PHARMACEUTICA, INC., JOHNSON & JOHNSON AND YOSHINOBU NAMIHIRA, M.D.

v.

BERTHA GRANT, ET AL.

DATE OF JUDGMENT: 01/10/2003 TRIAL JUDGE: HON. ROBERT G. EVANS COURT FROM WHICH APPEALED: SMITH COUNTY CIRCUIT COURT ATTORNEYS FOR APPELLANTS: DONNA BROWN JACOBS CHRISTY D. JONES JOHN C. HENEGAN ROBERT L. JOHNSON, III CLIFFORD C. WHITNEY, III R. E. PARKER, JR. ATTORNEYS FOR APPELLEES: JAMES W. NOBLES, JR. ANGELO JOHN DORIZAS EUGENE COURSEY TULLOS NATURE OF THE CASE: CIVIL - PERSONAL INJURY DISPOSITION: REVERSED AND REMANDED - 05/13/2004 MOTION FOR REHEARING FILED: MANDATE ISSUED:

BEFORE SMITH, C.J., COBB, P.J., AND CARLSON, J.

CARLSON, JUSTICE, FOR THE COURT:

¶1. Bertha Grant and three other Mississippi plaintiffs, Sarah Rebecca Garner, Tony Keen, and Daisy

James ("Plaintiffs"), filed suit in the Smith County Circuit Court alleging injuries they claimed were caused

by the prescription medication, Propulsid. The suit was filed against the New Jersey-based manufacturer

Janssen Pharmaceutica, Inc.; its New Jersey-based corporate parent Johnson & Johnson; a Mississippi physician from Warren County, Dr. Yoshinobu Namihira; and a pharmaceutical salesperson from Rankin

County, Eric Norsworthy. Only Grant is a resident of Smith County. Garner is a resident of Scott County,

and Keen and James are residents of Warren County. Also Keen and James, the two Warren County

residents, were the only two plaintiffs who were patients of Dr. Namihira, who is also a resident of Warren

County. The plaintiffs sought to hold the defendants jointly and severally liable to each plaintiff for

compensatory and punitive damages.

¶2. On November 1, 2002, Janssen and Johnson & Johnson filed a Motion to Sever and Transfer

Venue for Separate Trials, arguing that joinder was improper under Miss. R. Civ. P. 20 and that venue was

improper in Smith County. The trial court denied the motion as well as Janssen's and Johnson & Johnson's

ore tenus motion for certification of interlocutory appeal. On April 3, 2003, this Court granted Janssen's

and Johnson & Johnson's Petition for Interlocutory Appeal by Permission Pursuant to M.R.A.P. 5(a).

Finding that joinder was improper and that the trial court abused its discretion in denying the motion to

sever and transfer, we reverse the trial court's judgment and remand this case for severance and for a

transfer of the severed cases to those jurisdictions in which each plaintiff could have brought his or her

claims without reliance on another of the improperly joined plaintiffs.

FACTS1

¶3. Propulsid is a prescription medication manufactured by Janssen Pharmaceutica, Inc., used to treat

gastroesophageal reflux disease (GERD). The Food and Drug Administration (FDA) approved Propulsid

for sale in the United States in July 1993, after 12 years of research and clinical testing and more than five

years of use in Europe by millions of patients. The 1993 package insert noted that there had been rare

1 These facts are taken verbatim from Janssen Pharmaceutica, Inc. v. Armond, 866 So. 2d 1092, 1095 (Miss. 2004).

2 reports of tachycardia (rapid heartbeats) in patients taking Propulsid, but no incidents involving serious

injury or death. In late 1994, Janssen received two reports of patients who experienced a potentially fatal

heart arrhythmia known as "torsades de pointes." These patients were also taking the drug ketoconazole,

an antifungal medication. After a drug interaction study was performed, a new package insert was issued

in February 1995, warning against taking Propulsid with this and other medications. During the seven years

after FDA approval for sale in the U.S., the package insert for Propulsid was revised five times: in February

1995, October 1995, June 1998, May 1999 and January 2000. Along with the new package inserts,

Janssen sent hundreds of thousands of "Dear Doctor" letters to inform physicians and pharmacists of the

revised safety information. During the period from 1993 to 2000, there were reports of about 300 cardiac

events among the approximately ten million patients given Propulsid in the United States. Due to the

potential seriousness of such an event, Janssen decided to make Propulsid available only through an

investigational limited access program in May 2000. Janssen claims that this decision to withdraw Propulsid

fromcommercial distribution has sparked thousands of claims across the country that Propulsid has caused

all manner of injuries.

ANALYSIS

¶4. On February 19, 2004, this Court decided Janssen Pharmaceutica, Inc. v. Armond, 866

So. 2d 1092 (Miss. 2004). As in Armond, today’s case is a products liability suit based on the adequacy

of warnings which accompanied the medication, Propulsid. Armond controls the disposition of all issues

raised in the case sub judice. In Armond we determined that joinder was improper and that the trial court

abused its discretion in denying the motion to sever and transfer. Therefore, we reach the same conclusion

here.

CONCLUSION

3 ¶5. For these reasons, we reverse the trial court's judgment and remand this case for severance and

for a transfer of the severed cases to those jurisdictions in which each plaintiff could have brought his or

her claims without reliance on another of the improperly joined plaintiffs.

¶6. REVERSED AND REMANDED.

SMITH, C.J., WALLER AND COBB, P.JJ., AND GRAVES, J., CONCUR. DICKINSON, J., CONCURS WITH SEPARATE WRITTEN OPINION. EASLEY, J., DISSENTS WITH SEPARATE WRITTEN OPINION. DIAZ AND RANDOLPH, JJ., NOT PARTICIPATING.

DICKINSON, JUSTICE, CONCURRING:

¶7. I fully concur with the majority in this case. I write separately only to point out that I see no

justification for carving out an exception to the application of Rule 20 of the Mississippi Rules of Civil

Procedure for "mature torts," or in other words, asbestos cases. Rule 20 should apply equally to all torts,

whether mature or immature.

¶8. Therefore, I do not believe we were correct in Armond when we implied that plaintiffs bringing

asbestos claims may ignore the requirements of Rule 20 of the Mississippi Rules of Civil Procedure.

EASLEY, JUSTICE, DISSENTING:

¶9. I dissent from the majority's ruling today. The majority's decision follows on the heels of our recent

decision, Janssen Pharmaceutica, Inc. v. Armond, 866 So.2d 1092 (Miss. 2004), in which I joined

Justice Graves's specially concurring opinion.

¶10. In Armond, Justice Graves advocated the adoption of a class action rule instead of relying upon

Rule 20. In this case, as well as Armond, the majority provides little guidance in this new course of

proceeding. The majority is quick to hold that the Propulsid claims do not arise out of the same transaction

or occurrence, thus failing to meet the requirements of Rule 20. However, litigants, their lawyers, and the

4 trial courts are left without a clue as to how to proceed in cases. Armond was reversed and remanded

because the claims did not arise out of the same transactions or occurrence and their joinder prejudiced

the defendants. Id. at 1095 (¶7). Specifically, the Court reversed the trial court ruling and remanded the

case for severance of any defendant with no connection to Armond, including doctors that did not prescribe

Propulsid to Armond. Id.

¶11.

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Related

Janssen Pharmaceutica, Inc. v. Armond
866 So. 2d 1092 (Mississippi Supreme Court, 2004)
In Re Bristol-Myers Squibb Co.
975 S.W.2d 601 (Texas Supreme Court, 1998)

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