Johnson v. GlaxoSmithKline, Inc.

166 Cal. App. 4th 1497, 83 Cal. Rptr. 3d 607, 8 Cal. Daily Op. Serv. 12, 2008 Cal. App. LEXIS 1446
CourtCalifornia Court of Appeal
DecidedSeptember 19, 2008
DocketB199453
StatusPublished
Cited by57 cases

This text of 166 Cal. App. 4th 1497 (Johnson v. GlaxoSmithKline, Inc.) is published on Counsel Stack Legal Research, covering California Court of Appeal primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Johnson v. GlaxoSmithKline, Inc., 166 Cal. App. 4th 1497, 83 Cal. Rptr. 3d 607, 8 Cal. Daily Op. Serv. 12, 2008 Cal. App. LEXIS 1446 (Cal. Ct. App. 2008).

Opinion

Opinion

PERLUSS, P. J.

In two published decisions the United States District Court for the Central District of California denied class certification in putative class actions brought by current and former users of the prescription drug Paxil against GlaxoSmithKline, Inc. (GSK), the drug’s manufacturer, which alleged GSK had deceptively advertised Paxil as non-habit-forming. *1502 Relying upon those decisions and Alvarez v. May Dept. Stores Co. (2006) 143 Cal.App.4th 1223 [49 Cal.Rptr.3d 892] (Alvarez), which applied established principles of collateral estoppel to class certification issues, the trial court granted GSK’s motion for summary adjudication precluding this case from proceeding as a class action, ruling Kevin Johnson’s superior court lawsuit against GSK sought to certify the identical putative class, pursuing the same legal claims, as had been disallowed in the federal actions. Because the class issues actually litigated in the federal court Paxil cases differ from those presented by Johnson’s putative class action, we reverse.

FACTUAL AND PROCEDURAL BACKGROUND

1. Johnson’s First Amended Complaint

Paxil, a drug manufactured and distributed by GSK, is prescribed for conditions including depression, panic disorder and generalized anxiety disorder. On January 14, 2003 Johnson filed his original complaint and on July 15, 2003 filed a first amended putative class action complaint against GSK on behalf of all California residents who had taken Paxil after 1992 and had become addicted to it or had suffered withdrawal symptoms when they attempted to stop taking it. 1 The complaint asserted causes of action for negligent misrepresentation, concealment, negligence, strict product liability and violation of California’s unfair competition law (Bus. & Prof. Code, § 17200 et seq. (section 17200)), largely on the basis GSK had falsely and deceptively advertised Paxil as non-habit-forming.

Johnson alleged he was prescribed Paxil in early 2000 for moderate anxiety caused by the stress of work and family. Johnson further alleged, albeit without specifying the timing, that he had seen television and heard radio advertisements stating Paxil had few side effects and was not addictive; in addition, his doctor never informed him of any side effects or addiction-related symptoms. For a short while the drug was effective; Johnson felt euphoric and better able to deal with stress. Johnson, however, began suffering from fatigue and sexual dysfunction, motivating him to discontinue using Paxil in January 2002. When Johnson stopped, he experienced severe physical and emotional withdrawal symptoms, including headaches, heart palpitations and the sensation of electric shocks throughout his body. Even after one year Johnson continued to suffer from, among other symptoms, insomnia and the electric shock sensation. Johnson alleged he would not have taken Paxil had these symptoms been explained to him by his doctor, who himself was inadequately warned by GSK about these symptoms.

*1503 2. Johnson’s Class Definitions

The first amended complaint defined the putative class as “all California residents, who are not deceased, who have been prescribed, and have taken Paxil at any time after 1992, and who have suffered or continue to suffer from withdrawal episodes or symptoms, or those who have become addicted and/or [are] unable to stop taking Paxil for fear of these symptoms.” In response to the trial court’s request at a status conference for a definite class definition, in a joint statement filed June 25, 2004, the class definition was revised to include “all California residents, who are not deceased, who have been prescribed, and have taken Paxil at any time after 1992 until the present.”

3. GSK’s Motion for Summary Adjudication

On January 19, 2007 GSK filed a motion for summary adjudication to preclude Johnson’s lawsuit from proceeding as a class action. GSK asserted under the collateral estoppel principles applied to class action determinations by Division Four of this court in its then-recent decision in Alvarez, supra, 143 Cal.App.4th 1223, 2 United States Senior District Judge Mariana R. Pfaelzer’s decisions denying class certification in In re Paxil Litigation (C.D.Cal. 2003) 212 F.R.D. 539 (Paxil I) and In re Paxil Litigation (C.D.Cal. 2003) 218 F.R.D. 242 (Paxil II) barred Johnson’s class action claims. Johnson filed an opposition addressing the collateral estoppel issue; GSK replied; and the court heard oral argument on February 16, 2007. At the hearing the trial court requested further briefing on whether the denials of class certification in Paxil I and Paxil II satisfied all of the required elements for collateral estoppel. Following receipt of the supplemental briefs requested by the court, the matter was submitted.

a. Paxil I

On August 1, 2002 in Paxil I, supra, 212 F.R.D. 539, 542, the plaintiffs moved under rule 23 of the Federal Rules of Civil Procedure (28 U.S.C.) (rule 23) to certify five nationwide subclasses of Paxil users, differentiated by whether the user was still taking Paxil and the type of relief sought, in an action asserting claims including negligence, breach of express and implied warranty and violation of state unfair competition laws. The district court described the initial motion for class certification, including the proposed class definition, as deficient: “[Cjontrary to established Constitutional standards, [it] failed to take into account differences in state law. As well, the *1504 [m]otion improvidently downplayed the individual factual and legal issues that inevitably arise when prosecuting a personal injury tort lawsuit that centers around the effects of a pharmaceutical drug on the human body.” (Paxil I, at p. 542.) Consequently, the plaintiffs substantially modified the class definitions in their reply papers and proposed 12 subclasses, grouping together plaintiffs in states with similar laws. (Id. at pp. 542, 545.) One proposed subclass was for “[a]ll persons who have used Paxil and who reside in 3 states, including California which are identical to California’s [unfair competition law] where plaintiff need not show reliance, causation or damage.” In a footnote the plaintiffs argued, “If the court does not certify the five state subclasses then at the very least it should certify a subclass of California plaintiffs under the [unfair competition law].”

The district court denied the plaintiffs’ motion, generally finding they had failed “to define a manageable class” and had “failed to demonstrate that a manageable trial plan exist[ed] that would make a class action lawsuit feasible.” (Paxil I, supra, 212 F.R.D. at p.

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166 Cal. App. 4th 1497, 83 Cal. Rptr. 3d 607, 8 Cal. Daily Op. Serv. 12, 2008 Cal. App. LEXIS 1446, Counsel Stack Legal Research, https://law.counselstack.com/opinion/johnson-v-glaxosmithkline-inc-calctapp-2008.