Smith v. Janssen Pharmaceuticals , 695 F. App'x 408 ( 2017 )


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  •                                                                                 FILED
    United States Court of Appeals
    UNITED STATES COURT OF APPEALS                         Tenth Circuit
    FOR THE TENTH CIRCUIT                         August 14, 2017
    _________________________________
    Elisabeth A. Shumaker
    Clerk of Court
    BERNARD L. SMITH,
    Plaintiff - Appellant,
    v.                                                         No. 17-3057
    (D.C. No. 2:15-CV-09085-JAR)
    JANSSEN PHARMACEUTICALS, INC.;                               (D. Kan.)
    JOHNSON & JOHNSON COMPANY;
    JANSSEN RESEARCH AND
    DEVELOPMENT, LLC,
    Defendants - Appellees.
    _________________________________
    ORDER AND JUDGMENT*
    _________________________________
    Before LUCERO, BALDOCK, and MORITZ, Circuit Judges.
    _________________________________
    Bernard Smith, proceeding pro se, appeals the district court’s grant of
    summary judgment in favor of defendants in this product liability action. Exercising
    jurisdiction under 
    28 U.S.C. § 1291
    , we affirm.
    *
    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. This order and judgment is not binding
    precedent, except under the doctrines of law of the case, res judicata, and collateral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.
    I
    Smith began taking the medication Risperdal in 2007 to treat certain mental
    health conditions. In July 2008, he switched to a generic version of the drug—
    Risperidone—which he continued to use until February 2014. During this period, he
    was also prescribed at least two other antipsychotic medications—Haloperidol and
    Thiothixene.
    In February 2014, Smith began complaining of sore, enlarged, and leaking
    breasts. He told medical staff that he had been diagnosed with galactorrhea and
    gynecomastia in 2007, and that a lawyer had advised him to document those
    conditions in his medical records. However, there is no record of a 2007 diagnosis,
    and physical exams in 2014 and 2015 did not reveal any abnormal breast enlargement
    or discharge, causing at least one doctor to reject the possibility that Smith was
    suffering from gynecomastia.
    In April 2015, Smith filed a pro se complaint in state court against Janssen
    Pharmaceuticals, Inc., Johnson & Johnson, and Janssen Research & Development,
    LLC (collectively “defendants”), alleging that Risperdal had caused him to
    experience extreme weight gain and gynecomastia. Defendants removed the case to
    federal court on the basis of diversity jurisdiction. After discovery was complete,
    they moved for summary judgment. Interpreting Smith’s complaint as asserting a
    product liability claim, the district court granted the motion. It concluded there was
    no evidence that Smith had been diagnosed with gynecomastia or galactorrhea, or
    2
    that his alleged physical symptoms were caused by ingestion of Risperdal. Smith
    timely appealed.
    II
    We review a district court’s grant of summary judgment de novo. Koch v.
    City of Del City, 
    660 F.3d 1228
    , 1237 (10th Cir. 2011). Summary judgment is
    appropriate if “there is no genuine dispute as to any material fact and the movant is
    entitled to judgment as a matter of law.” Fed. R. Civ. P. 56(a). In applying this
    standard, “we view the evidence and draw reasonable inferences therefrom in the
    light most favorable to the nonmoving party.” Fowler v. United States, 
    647 F.3d 1232
    , 1237 (10th Cir. 2011) (quotation omitted).
    Smith’s product liability claim is governed by the Kansas Product Liabilities
    Act (“KPLA”), Kan. Stat. § 60-3301 et seq. See McPhail v. Deere & Co., 
    529 F.3d 947
    , 957 (10th Cir. 2008) (applying substantive law of forum state in diversity
    action); Savina v. Sterling Drug, Inc., 
    795 P.2d 915
    , 931 (Kan. 1990) (noting KPLA
    “applies to all product liability claims regardless of the substantive theory of
    recovery”). Smith may recover under this statute only if he can show that he suffered
    an injury caused by defendants’ product. See Jenkins v. Amchem Prods., Inc., 
    886 P.2d 869
    , 886 (Kan. 1994).
    We agree with the district court that Smith has failed to demonstrate either
    injury or causation. There is no evidence in the record—aside from Smith’s own
    unsupported assertions—that he was ever diagnosed with gynecomastia or
    galactorrhea, and his physical exams from 2014 and 2015 indicate that he did not
    3
    suffer from any symptoms related to those conditions. To the extent Smith alleges
    other injuries, such as weight gain, there is nothing in the record to support a
    conclusion that those injuries resulted from his limited use of Risperdal.
    III
    AFFIRMED. Smith’s motion to proceed in forma pauperis is GRANTED,
    but we remind him of his obligation to continue making payments until the filing fee is
    paid in full. See 
    28 U.S.C. § 1915
    (b).
    Entered for the Court
    Carlos F. Lucero
    Circuit Judge
    4
    

Document Info

Docket Number: 17-3057

Citation Numbers: 695 F. App'x 408

Filed Date: 8/14/2017

Precedential Status: Non-Precedential

Modified Date: 1/13/2023