In Re Diet Drugs (Phentermine, Fenfluramine, Dexfenfluramine) Products Liability Litigation

553 F. Supp. 2d 442, 2008 WL 942592
CourtDistrict Court, E.D. Pennsylvania
DecidedApril 9, 2008
DocketMDL Docket No. 1203. Civil Action No. 99-20593
StatusPublished
Cited by27 cases

This text of 553 F. Supp. 2d 442 (In Re Diet Drugs (Phentermine, Fenfluramine, Dexfenfluramine) Products Liability Litigation) is published on Counsel Stack Legal Research, covering District Court, E.D. Pennsylvania primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In Re Diet Drugs (Phentermine, Fenfluramine, Dexfenfluramine) Products Liability Litigation, 553 F. Supp. 2d 442, 2008 WL 942592 (E.D. Pa. 2008).

Opinion

MEMORANDUM AND PRETRIAL ORDER NO. 7763

BARTLE, Chief Judge.

Before the court is a renewed joint petition for a final award of counsel fees and expense reimbursements (“Joint Petition”) in connection with the Diet Drug Nationwide Class Action Settlement Agreement (“Settlement Agreement”) with Wyeth 1 and in connection with the multidistrict litigation involving Wyeth’s diet drugs known as “fen-phen.” The Joint Petition has been filed by a large group of law firms consisting primarily of the Plaintiffs’ Management Committee and Class Counsel for claimants under the Settlement Agreement (hereinafter “Joint Fee Applicants”) and is joined by some of the major filers in this multidistrict litigation (hereinafter “Major Filers”), who collectively constitute the “Joint Petitioners.” The Joint Fee Applicants seek fees and costs from four different sources: (1) the Fund A Escrow Account established pursuant to the Settlement Agreement; (2) the Fund B Attorneys’ Fees Account established pursuant to the Settlement Agreement; (3) the Supplemental Class Settlement Fund established pursuant to the Seventh Amendment to the Settlement Agreement; and (4) the MDL 1203 Fee and Cost Account. The Joint Petitioners also request incentive awards for representative plaintiffs in two class actions. Two sets of objections 2 have been timely filed in re *449 sponse to the Joint Petition and a renewed motion for incentive awards has been filed by named plaintiffs in three class actions.

I. BACKGROUND

A detailed description of the early course of this litigation, including the factual basis for liability, the medical circumstances of the Class Members, and the provisions of the Settlement Agreement, can be found in this court’s Pretrial Order (“PTO”) No. 1415, 2000 WL 1222042 (E.D.Pa. Aug.28, 2000), entered by my predecessor Judge Louis C. Bechtle. We will summarize the relevant background and chronology of this litigation.

From 1989 through September, 1997, Wyeth marketed and sold two prescription drugs for weight loss in the United States under the brand names Pondimin (fenflu-ramine) and Redux (dexfenfluramine) (hereinafter “diet drugs”). Beginning in 1992, physicians commonly prescribed Pondimin in combination with phenter-mine, another prescription diet drug. Phentermine was and still is distributed and sold under several different brand names. The combination of Pondimin with phentermine was often referred to as “fen-phen.” Wyeth had significant sales of both Pondimin and Redux in the mid-1990’s. From January, 1995 until mid-September, 1997, approximately four million persons in the United States took Pondimin. Similarly, from June, 1996 through September, 1997, two million people in this country used Redux.

During the period from March to August, 1997 the Mayo Clinic in Rochester, Minnesota observed and reported an association between the use of fenfluramine and/or dexfenfluramine and valvular heart disease (“VHD”). On September 15, 1997, Wyeth and the Food and Drug Administration (“FDA”) announced that there would be no further sales of Pondimin and Redux in the United States. Since that time, epidemiological studies have established a causal relationship between fenflu-ramine and dexfenfluramine and VHD. These studies have also determined that fenfluramine and dexfenfluramine cause a fatal but rare disease known as primary pulmonary hypertension (“PPH”). 3

A tidal wave of litigation followed the withdrawal of Pondimin and Redux. Individuals who had ingested diet drugs filed lawsuits and class actions in federal and state courts against Wyeth and other defendants, including manufacturers, distributors, weight-loss clinics, pharmacies and physicians. On December 10, 1997, the Judicial Panel on Multidistrict Litigation (the “JPML”) designated the United States District Court for the Eastern District of Pennsylvania as the transferee court for IN RE: DIET DRUGS (PHEN-TERMINE/FENFLURAMINE/DEX-FENFLURAMINE) PRODUCTS LIABILITY LITIGATION, MDL 1203 (“MDL 1203”). See 28 U.S.C. § 1407. All cases filed in the federal judicial system were subsequently transferred to the Eastern District of Pennsylvania for coordinated and consolidated pretrial proceedings. To date, at least 105,000 plaintiffs have filed lawsuits, over 130 class actions were transferred to the MDL and the claims of more than 35,000 plaintiffs have been transferred by the JPML to this court.

Shortly after the first transfer of cases to MDL 1203, the court established the *450 Plaintiffs’ Management Committee (“PMC”) to oversee the coordinated and consolidated pretrial proceedings and to conduct discovery of widespread applicability on behalf of plaintiffs in MDL 1203. See PTO No. 6 (Feb. 5, 1998). As part of its duties and responsibilities, the PMC assisted and continues to assist all plaintiffs in MDL 1203 and state-federal coordinated proceedings by appearing frequently before this court, attending regular status conferences held by the Special Discovery Master, Gregory P. Miller, Esq., preparing motions and responses regarding case-wide discovery matters and other pretrial issues, and maintaining a document depository for all documents produced in MDL 1203.

The PMC was also charged with establishing a Discovery Committee, which consisted of PMC members as well as additional lawyers representing plaintiffs in various state courts. See PTO 38 ¶¶ 1, 2 (Apr. 21, 1998). The PMC Discovery Committee coordinated and completed numerous depositions of defendants’ corporate representatives, employees and generic experts. The court permitted the PMC and the co-chairs of the PMC Discovery Committee to assign work to other “common benefit” attorneys (“PMC common benefit attorneys”). The members of the PMC, 4 the PMC Discovery Committee, 5 and the PMC common benefit attorneys 6 are all Joint Fee Applicants in this matter.

In late April, 1999, Wyeth and a coalition of plaintiffs’ attorneys consisting of the PMC and counsel for plaintiffs in certified state class actions pending in Illinois, New Jersey, New York, Pennsylvania, Texas, Washington, and West Virginia began negotiations for a global resolution of the diet drug litigation. 7 As a result of the *451 negotiations the parties executed the Settlement Agreement on November 18, 1999. Five days later the court granted preliminary approval of the settlement. PTO No. 997 ¶ 6 (Nov. 23, 1999). At that time, the court also set forth procedures for providing notice and conducting discovery in preparation for the fairness hearing. From May 2, 2000 through May 11, 2000 the court held a hearing to consider the fairness, reasonableness and adequacy of the settlement. 8 The court approved the Settlement Agreement on August 28, 2000 in Pretrial Order No. 1415. Appeals of Pretrial Order No. 1415 followed.

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Cite This Page — Counsel Stack

Bluebook (online)
553 F. Supp. 2d 442, 2008 WL 942592, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-diet-drugs-phentermine-fenfluramine-dexfenfluramine-products-paed-2008.