Watson v. Mylan Pharmaceuticals

CourtCourt of Appeals for the Tenth Circuit
DecidedDecember 18, 2019
Docket19-3162
StatusUnpublished

This text of Watson v. Mylan Pharmaceuticals (Watson v. Mylan Pharmaceuticals) is published on Counsel Stack Legal Research, covering Court of Appeals for the Tenth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Watson v. Mylan Pharmaceuticals, (10th Cir. 2019).

Opinion

FILED United States Court of Appeals UNITED STATES COURT OF APPEALS Tenth Circuit

FOR THE TENTH CIRCUIT December 18, 2019 _________________________________ Elisabeth A. Shumaker Clerk of Court CARMEN WATSON,

Plaintiff - Appellant,

v. No. 19-3162 (D.C. No. 5:18-CV-04137-CM-JPO) MYLAN PHARMACEUTICALS; (D. Kan.) MYLAN N.V.; MYLAN LABS; GENPHARM; BERTEK; MERCK; MYLAN INC.; RAJIV MALIK; HEATHER BRESCH; CATALENT PHARMA SOLUTIONS,

Defendants - Appellees. _________________________________

ORDER AND JUDGMENT* _________________________________

Before MATHESON, McKAY, and BACHARACH, Circuit Judges.** _________________________________

Pro se Plaintiff Carmen Watson appeals from the district court’s dismissal of

her product-liability claims on the grounds that they are subject to claim preclusion

and barred by the statute of limitations.

* This order and judgment is not binding precedent, except under the doctrines of law of the case, res judicata, and collateral estoppel. It may be cited, however, for its persuasive value consistent with Fed. R. App. P. 32.1 and 10th Cir. R. 32.1. ** After examining the briefs and appellate record, this panel has determined unanimously that oral argument would not materially assist in the determination of this appeal. See Fed. R. App. P. 34(a)(2); 10th Cir. R. 34.1(G). The case is therefore ordered submitted without oral argument. On June 21, 2016, Plaintiff filed a pro se complaint against Mylan

Pharmaceuticals and Mylan Inc. in federal district court alleging she had sustained

numerous injuries after taking the defendants’ anti-acne drug, Amnesteem—an FDA-

approved generic version of the brand-name drug Accutane—in 2014. Plaintiff

claimed the defendants failed to warn her of Amnesteem’s deleterious side-effects in

violation of Kansas law. The district court dismissed the action, concluding that

Plaintiff’s claim was preempted by federal law.1 See Watson v. Mylan Pharma., Inc.,

No. 16-2449, 2016 WL 6996263, at *2–5 (D. Kan. Nov. 30, 2016).

On appeal, we agreed that Plaintiff’s claim was preempted. See Watson v.

Mylan Pharma., Inc., 701 F. App’x 729, 731–32 (10th Cir. 2017). We noted Plaintiff

had attempted to overcome preemption analysis on appeal by arguing that

Amnesteem’s label was deficient because it had failed to keep pace with updates to

Accutane’s label. Id. at 731. Although we acknowledged that a failure-to-update

theory was potentially viable,2 we rejected Plaintiff’s argument because she did not

assert the theory in her complaint, argue it in her motion-to-dismiss or motion-for-

reconsideration briefing, move to amend in order to include it in her complaint, or

1 See PLIVA, Inc. v. Mensing, 564 U.S. 604, 611–13, 617, 624 (2011) (holding that state tort law that required generic drug manufacturers to provide adequate warning labels was preempted where federal law required manufacturers to use the same labels as their brand-name counterparts); Mut. Pharm. Co. v. Bartlett, 570 U.S. 472, 476 (2013) (holding “state-law design-defect claims that turn on the adequacy of a drug’s warnings are pre-empted by federal law under PLIVA”). 2 Compare Fulgenzi v. PLIVA, Inc., 711 F.3d 578, 584 (6th Cir. 2013), with Morris v. PLIVA, Inc., 713 F.3d 774, 777 (5th Cir. 2013) (per curiam). 2 explain how the defendants’ failure to update Amnesteem’s label proximately caused

her alleged injuries. Id. at 731–2. We accordingly affirmed the dismissal. Id.

On July 16, 2018, Plaintiff filed a new complaint in New Jersey state court3

and, after dismissal, re-filed it in the Kansas federal district court on November 13,

2018. As with her previous complaint, Plaintiff seeks to recover for injuries she

allegedly sustained after taking Amnesteem in 2014. However, Plaintiff’s new

complaint names six additional corporate Defendants as well as two individual

Defendants. Plaintiff also expressly asserts a failure-to-update theory and alleges

newly diagnosed injuries she claims could not have been ascertained at the time she

brought her prior suit.

The district court dismissed the complaint. The court concluded Plaintiff’s

cause of action against the two individual Defendants and four of the corporate

Defendants—Mylan Inc., Mylan Pharmaceuticals, Mylan N.V., and Catalent Pharma

Solutions—was subject to claim preclusion. The court determined that the dismissal

of the previous complaint constituted a judgment on the merits and that the six

3 Plaintiff apparently filed her complaint in New Jersey based on the New Jersey Supreme Court’s decision to designate the Atlantic County Court as the forum to address “all pending and future New Jersey product-liability actions involving Accutane.” See In re Accutane Litig, 194 A.3d 503, 512 (N.J. 2018). New Jersey state court records show that Plaintiff’s complaint against Mylan NV, Mylan Labs, Mylan Pharmaceuticals, Catalent Pharma Solution, Rajiv Malik, Mylan Inc., and Genpharm, filed in Atlantic County Court on July 16, 2018, was dismissed without prejudice on August 14, 2018. See Watson v. Mylan Pharma., No. ATL L-001708-18 (Atlantic County Ct.); see also Stan Lee Media, Inc. v. Walt Disney Co., 774 F.3d 1292, 1298 n.2 (10th Cir. 2014) (explaining that we may take judicial notice of another court’s docket). Plaintiff asserts that the state court instructed her to refile in Kansas, where she resides. 3 Defendants at issue were either identical to, or in privity with, the defendants in the

previous case. The court also concluded that, under the transactional approach

employed in the Tenth Circuit, see MACTEC, Inc. v. Gorelick, 427 F.3d 821, 832

(10th Cir. 2005), the cause of action asserted in the new complaint—even formulated

as a failure-to-update theory—was identical, for purposes of claim preclusion, to the

cause of action adjudicated in Plaintiff’s previous suit.

The district court concluded Plaintiff’s state-law product-liability claims

against the remaining Defendants—Mylan Labs, Genpharm, Bertek, and Merck—

were barred by Kansas’s two-year statute of limitations. See Kan. Stat. Ann. § 60-

513. The court explained that Plaintiff had ascertained her alleged substantial

injuries from her use of Amnesteem no later than June 21, 2016, when she filed her

previous suit, and that, by the time she filed the instant suit, the two-year period had

run.4 The court also rejected Plaintiff’s contention that the statute of limitations

should be tolled under the doctrines of equitable estoppel and fraudulent

concealment, concluding that Plaintiff had failed to allege the requirements for

equitable estoppel or to plead fraudulent concealment with particularity.

In the dismissal order, the district court also denied Plaintiff’s motions for

entry of default and default judgment against the individual Defendants, Rajiv Malik

and Heather Bresch.

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Related

Benne v. International Business MacHines Corp.
87 F.3d 419 (Tenth Circuit, 1996)
MACTEC, Inc. v. Gorelick
427 F.3d 821 (Tenth Circuit, 2005)
Sanchez v. Triple-S Management, Corp.
492 F.3d 1 (First Circuit, 2007)
Eleanor Fulgenzi v. PLIVA, Inc.
711 F.3d 578 (Sixth Circuit, 2013)
Roe v. Diefendorf
689 P.2d 855 (Supreme Court of Kansas, 1984)
Stan Lee Media, Inc. v. Walt Disney Co.
774 F.3d 1292 (Tenth Circuit, 2014)
Watson v. Mylan Pharmaceuticals, Inc.
701 F. App'x 729 (Tenth Circuit, 2017)
Malouf v. SEC. & Exch. Comm'n
933 F.3d 1248 (Tenth Circuit, 2019)
PLIVA, Inc. v. Mensing
180 L. Ed. 2d 580 (Supreme Court, 2011)
In re Accutane Litig.
194 A.3d 503 (Supreme Court of New Jersey, 2018)
Morris v. PLIVA, Inc.
713 F.3d 774 (Fifth Circuit, 2013)
Valido-Shade v. Wyeth, LLC
875 F. Supp. 2d 474 (E.D. Pennsylvania, 2012)
Mut. Pharm. Co. v. Bartlett
570 U.S. 472 (Supreme Court, 2013)

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