Peter Casey v. Bristol-Myers Squibb Company ( 2018 )


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  •      Case: 18-50380      Document: 00514701725         Page: 1    Date Filed: 10/29/2018
    IN THE UNITED STATES COURT OF APPEALS
    FOR THE FIFTH CIRCUIT
    United States Court of Appeals
    Fifth Circuit
    No. 18-50380                                 FILED
    Summary Calendar                         October 29, 2018
    Lyle W. Cayce
    Clerk
    PETER B. CASEY,
    Plaintiff - Appellant
    v.
    BRISTOL-MYERS SQUIBB COMPANY; OTSUKA AMERICA
    PHARMACEUTICAL, INCORPORATED,
    Defendants - Appellees
    Appeal from the United States District Court
    for the Western District of Texas
    USDC No. 5:17-CV-1175
    Before JOLLY, COSTA, and HO, Circuit Judges.
    PER CURIAM:*
    Peter Casey alleges that he began taking Abilify in 2011, after it was
    prescribed to him by his psychologist. In June 2016, he stopped taking Abilify
    following a three week “tapering off” period.            He alleges that withdrawal
    symptoms manifested two weeks later. These allegedly included headaches,
    weight loss, insomnia, impotence, and, most importantly, Tardive Dyskensia,
    * Pursuant to 5TH CIR. R. 47.5, the court has determined that this opinion should not
    be published and is not precedent except under the limited circumstances set forth in 5TH
    CIR. R. 47.5.4.
    Case: 18-50380       Document: 00514701725         Page: 2    Date Filed: 10/29/2018
    No. 18-50380
    a neurological disorder that causes repetitive, unintentional movements.
    Casey filed suit against defendants, manufacturers and marketers of Abilify,
    in Texas state court asserting a state law failure-to-warn claim.                       The
    defendants removed the case to federal district court. The district court then
    dismissed the case, finding that the defendants were entitled to a judgment on
    the pleadings because, under Texas law, there is a presumption that warnings
    approved by the United States Food and Drug Administration (FDA) are
    “adequate.” See Tex. Civ. Prac. & Rem. Code § 82.007.
    Casey makes two arguments on appeal. First, he suggests that the
    defendants misled or withheld from the FDA material information causally
    related to the side effects that he suffered, thus rebutting the state law
    presumption and plausibly stating a cognizable claim. Fraud on the FDA is
    one of the exceptions set forth in the Texas statute as capable of rebutting the
    presumption against liability. Tex. Civ. Prac. & Rem. Code § 82.007(b)(1). We
    have previously held, however, that federal law requires a plaintiff suing under
    a state law failure-to-warn cause of action to show that the FDA itself has
    found that defendants behaved fraudulently. Loften v. McNeil Consumer &
    Specialty Pharms., 
    672 F.3d 372
    (5th Cir. 2012).                     Despite conclusory
    statements in his brief, Casey’s complaint does not allege this, let alone contain
    any specific factual matter to support it.        Therefore, the district court did not
    err in its ruling concerning fraud on the FDA. 1
    1The district court presumed that Casey was required to plead facts to rebut the Texas
    law presumption in his complaint. We have not previously decided in a published opinion
    whether Tex. Civ. Prac. & Rem. Code § 82.007 establishes an additional element of a failure-
    to-warn claim that must be adequately pled by the plaintiff, or an affirmative defense, which
    does not. We have presumed the former, however, in at least one unpublished opinion.
    Thurston v. Merck & Co., 415 F. App’x 585 (5th Cir. 2011). Because Casey does not raise this
    issue on appeal, we need not address it.
    2
    Case: 18-50380   Document: 00514701725     Page: 3   Date Filed: 10/29/2018
    No. 18-50380
    Second, Casey argues that the district court erred because, by labeling
    his symptoms “side effects” rather than “withdrawal” symptoms, the
    defendants gave per se inadequate warnings.        We see no merit to this
    argument. Leaving aside whether there is a meaningful difference between
    labeling the symptoms generally as “side effects” or explicitly attaching the
    “withdrawal” label to them, this is not a decision for us to make. The FDA has
    approved the warning provided by the defendants, and Texas law has made
    this approval sufficient to forestall any products liability claim absent the
    existence of a specified exception. Since Casey has not adequately pled any of
    these exceptions, we have no basis for finding that the defendants may be held
    liable.
    Therefore, we AFFIRM the judgment of the district court.
    3
    

Document Info

Docket Number: 18-50380

Filed Date: 10/29/2018

Precedential Status: Non-Precedential

Modified Date: 10/30/2018