Wood v. Wyeth-Ayerst Laboratories, Division of American Home Products

82 S.W.3d 849, 2002 Ky. LEXIS 167, 2002 WL 1940664
CourtKentucky Supreme Court
DecidedAugust 22, 2002
Docket2000-SC-1067-DG
StatusPublished
Cited by52 cases

This text of 82 S.W.3d 849 (Wood v. Wyeth-Ayerst Laboratories, Division of American Home Products) is published on Counsel Stack Legal Research, covering Kentucky Supreme Court primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Wood v. Wyeth-Ayerst Laboratories, Division of American Home Products, 82 S.W.3d 849, 2002 Ky. LEXIS 167, 2002 WL 1940664 (Ky. 2002).

Opinion

GRAVES, Justice.

I.

In 1973, the United States Federal Food and Drug Administration approved the use and sale of fenfluramine, an appetite suppressing diet medication. The drug was tested, manufactured, and packaged by A.H. Robins and sold by Wyeth-Ayerst Laboratories, under the trade name Pondi-min. Appellees, American Home Products Corporation (hereinafter referred to collectively as “AHPC”), of which Wyeth-Ayerst is a division, also marketed another FDA-approved medication for obesity containing fenfluramine, called Redux. Demand for fenfluramine soared during the mid-1990’s, when people began using it along with phentermine in a diet drug combination known as “Fen-Phen.” The FDA never approved this drug combination.

In response to reports linking fenflura-mine consumption to an increased risk of *851 heart valve regurgitation, and apparently under pressure from the FDA, AHPC withdrew both Pondimin and Redux from the market in September 1997. Since then, many medical studies have confirmed the relationship between fenfluramine use and heart valve abnormalities.

In November 1999, AHPC entered into a “Nationwide Class Action Settlement Agreement” to redress physical injuries of fenfluramine users and provide medical screening to detect health problems arising in others in the future. Appellant, Erma Rae Wood, and many others “opted out” of this settlement because it specifically excluded claims for primary pulmonary hypertension, an often fatal disease stemming from decreased blood flow between the heart and lungs. Appellant seeks relief instead in the immediate suit. She has filed a motion for class certification under CR 23, requesting designation of the suit as a class action with her as the class representative.

Appellant claims to have used the drug fenfluramine from June to December of 1996, and she alleges her exposure to the hazardous substance was the result of AHPC’s negligence. In her complaint, Appellant, on behalf of a proposed class, seeks the following relief: (1) court-supervised notice and medical monitoring to enable people who have ingested Fen-Phen to be monitored for the existence of potentially dangerous side effects caused by the drags, including, but not limited to, valvular heart disease, primary pulmonary hypertension, and for altered serotonin levels and associated cognitive and/or neurophy-siological manifestations of impairment or injury; (2) a fund to pay for such monitoring and also medical research concerning the effects of the drags; (3) reimbursement of the costs of the drugs and/or previously incurred examination costs; and (4) punitive damages. Appellant has advanced various theories of liability as bases for recovery, including negligence, strict liability, concert of action, and enterprise liability.

The trial court dismissed Appellant’s complaint for failure to state a claim upon which relief can be granted, pursuant to CR 12.02. A motion for dismissal for failure to state a claim should only be granted if it appears the pleading party could not prove any set of facts in support of his claim that would entitle him to relief. Pari-Mutuel Clerks’ Union of Kentucky, Local 541, SEIU, AFL-CIO v. Kentucky Jockey Club, Ky., 551 S.W.2d 801, 803 (1977). The trial court concluded that Kentucky law requires a plaintiff to prove some present physical injury to support a tort claim, and Appellant had proven no such injury. The Court of Appeals upheld the trial court’s decision dismissing the case, also finding that Appellant did not allege in her complaint any “present physical harm as a result of her ingestion of Fen-Phen.” Appellant then petitioned this Court for review. There being recent developments in toxic tort litigation in other states, we granted discretionary review to address the important issues raised by Appellant regarding prospective relief for past exposure.

Appellant’s complaint specifies as her injury, and that of the class she seeks to represent, “significantly increased risk of serious injury and disease.” She further claims that she and others will “probably ... be required to pay sums to ascertain the existence, nature and extent of their injuries in the future.” In support of her claim, Appellant cites to many articles from various medical journals in which experts have recommended ongoing diagnostic testing for people who took fenflu-ramine. Notwithstanding these expert opinions, recovery on a theory of tort, like negligence or strict liability as sought *852 here, requires a plaintiff to show some present physical injury to support a cause of action. Appellant has offered no proof that she suffers from any injury at the present time resulting from her contact with or ingestion of fenfluramine. As such, Appellant has failed to state a claim upon which relief can be granted and her cause of action has not accrued. We therefore affirm the Court of Appeals in dismissing the complaint.

II.

This Court has consistently held that a cause of action in tort requires a present physical injury to the plaintiff. As early as Louisville & N.R. Co. v. Roberts, 207 Ky. 310, 269 S.W. 333, 334 (1925), and again in Kentucky Traction & Terminal Co. v. Roman’s Guardian, 232 Ky. 285, 23 S.W.2d 272 (1929), our predecessor Court refused to grant recovery for fright without any physical impact to support a cause of action. Later, in Morgan v. Hightower’s Adm’r., 291 Ky. 58, 163 S.W.2d 21 (1942), the Court declined to permit recovery for mental distress unaccompanied by physical harm, noting that “In a long and unbroken line of decisions this Court has held that [such] an action will not lie.” More recently, the Court has maintained the same position:

A cause of action does not exist until the conduct causes injury that produces loss or damage. The action for negligence evolved chiefly out of the old common-law form of action on the case, and it has always retained the rule of that action, that proof of damage was an essential part of the plaintiffs case.

Saylor v. Hall, Ky., 497 S.W.2d 218, 225 (1973).

In addition to her negligence claim, Appellant seeks redress on a theory of strict liability. Just as a negligence claim must be supported by a resulting physical injury, so must a claim based on strict liability. The Kentucky Court of Appeals adopted the view of the Restatement when it held, “To prevail in an action based upon strict products liability, a plaintiff must establish: (1) that there is a ‘product,’ which ... (5) results in physical harm to the user or consumer or his property.” Radcliff Homes, Inc. v. Jackson, Ky.App., 766 S.W.2d 63, 68 (1989) (citing Restatement (Second) of Torts § 402A (1965)). We agree that this is a correct statement of the law.

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Bluebook (online)
82 S.W.3d 849, 2002 Ky. LEXIS 167, 2002 WL 1940664, Counsel Stack Legal Research, https://law.counselstack.com/opinion/wood-v-wyeth-ayerst-laboratories-division-of-american-home-products-ky-2002.