Czimmer v. Janssen Pharmaceuticals, Inc.

122 A.3d 1043, 2015 Pa. Super. 175, 2015 Pa. Super. LEXIS 473, 2015 WL 4940819
CourtSuperior Court of Pennsylvania
DecidedAugust 20, 2015
Docket459 EDA 2014
StatusPublished
Cited by55 cases

This text of 122 A.3d 1043 (Czimmer v. Janssen Pharmaceuticals, Inc.) is published on Counsel Stack Legal Research, covering Superior Court of Pennsylvania primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Czimmer v. Janssen Pharmaceuticals, Inc., 122 A.3d 1043, 2015 Pa. Super. 175, 2015 Pa. Super. LEXIS 473, 2015 WL 4940819 (Pa. Ct. App. 2015).

Opinions

OPINION BY

MUNDY, J.:

Appellant, Janssen Pharmaceuticals, Inc. (Janssen),1 appeals from the trial court’s order entering judgment in favor of Appellee, April Czimmer, 'as guardian of Blake Czimmer, a minor,2 following a jury trial. After careful review, we affirm.

We take the relevant facts and procedural history of this case from the trial court’s January 2, 2014 opinion and our independent review of the record. April has a history of migraine headaches dating back to when she was a young teenager.3 In August 2006, physician’s assistant Lisa Basye prescribed Topamax4 to April to treat, her migraines, and April continued to use the drug until February 2007. At the time Basye prescribed Topamax to April, the Food and Drug Administration (FDA) categorized it as a Pregnancy Category C drug.5

In December 2006, April became pregnant with her son, Blake. Blake was born [1049]*1049on September 24, 2007, with a severe cleft lip and cleft palate with a hole above his lip. Since his birth, he has undergone four surgeries to repair his oral clefts and associated injuries. Blake will need to undergo a number of surgeries in the future, including jaw reconstruction and a bone graft at the time of maturity. He will also need speech therapy, treatment for his hearing, and a psychological evaluation.

On May 31, 2011, April commenced this lawsuit against Janssen by filing a writ of summons in the Philadelphia County Court of Common Pleas. On November 7, 2011, she filed a short-form complaint against Janssen alleging, in part, that it negligently failed to warn, her prescribing health care provider of the risks of potential birth defects associated with Topamax, including cleft lip and/or palate, if used during pregnancy. On March 25, 2013, Janssen filed a motion for summary judgment, which the trial court granted in part and denied in part.6

On October 15, 2013, the case proceeded to a jury trial on the negligent failure to warn claim. On October 30, 2013, the jury returned a verdict in favor of April, as guardian of Blake. It awarded $4,002,184.68 in damages, comprised of $3,440,000.00 for the non-economie loss of pain and suffering and $562,184.68 for future health care costs. On November 8, 2013, Janssen filed a post-trial motion requesting the trial court to grant judgment notwithstanding the verdict (JNOV) or a new trial. On January 2, 2014, the trial court entered an order and opinion denying Janssen’s post-trial motion. The trial court also entered judgment on the jury’s verdict, adding $207,713.38 in delay damages, resulting in a total judgment against Janssen for $4,209,898.06. This timely appeal followed.7

On appeal, Janssen raises the following issues for our review.

1. Does federal law preempt a state law negligent failure to warn claim where (a) [Janssen] could not have provided [April’s] proposed warning without [1050]*1050the Food and Drug Administration’s pri- or permission and assistance, and/or (b) there was clear evidence that [the] FDA would not have approved that proposed warning?
2. In a case governed by Virginia law, did the trial court err in applying a “substantial factor” standard of causation that the Supreme Court of Virginia has expressly rejected as contrary to the law of Virginia?
3. Did the trial court err (a) by permitting a negligent failure to warn claim to proceed to the jury in an action involving a prescription drug warning, when the prescribers of that drug testified that they knew, at the time they prescribed the drug, of the alleged risk of harm that formed the basis of the claim, and/or (b) by excluding relevant evidence related to those prescribers’ knowledge of the risk?
4. Did the trial court err (a) by permitting an award of damages for Blake Czimmer’s future healthcare costs incurred during his minority, when his parents’ claim for those damages was time-barred and Blake did not have a right of action to recover them, and/or (b) by failing to ask the jury to decide whether the parents had brought their claim within the applicable limitations period?

Janssen’s Brief at 5.

We begin by stating our standard of review of a trial court’s denial of post-trial motions for JNOV and a new trial.

An appellate court will reverse a trial court’s grant or denial of a JNOV only when the appellate court finds an abuse of discretion or an error of law. Our scope of review with respect to whether judgment n.o.v. is appropriate is plenary, as with any review of questions of law.
In reviewing a motion for judgment n.o.v., the evidence must be considered in the light most favorable to the verdict winner, and he must be given the benefit of every reasonable inference of fact arising therefrom, and any conflict in the evidence must be resolved in his favor. Moreover, a judgment n.o.v. should only be entered in a clear case and any doubts must be resolved in favor of the verdict winner. Further, a judge’s ap-praisement of evidence is not to be based on how he would have voted had he been a member of the jury, but on the facts as they come through the sieve of the jury’s deliberations.
There are two bases upon which a judgment n.o.v. can be entered: one, the movant is entitled to judgment as a matter of law, ... and/or two, the evidence was such that no two reasonable minds could disagree that the outcome should have been rendered in favor of the movant[.] With the first a court reviews the record and concludes that even with all factual inferences1 decided adverse to the movant the law nonetheless requires a verdict in his favor, whereas with the second the court reviews the evidentiary record and concludes that the evidence was such that a verdict for the movant was beyond peradventure.
Questions of credibility and conflicts in the evidence are for the [fact-finder] to resolve and the reviewing court should not reweigh the evidence. If there is any basis upon which the jury could have properly made its award, the denial of the motion for judgment n.o.v. must be affirmed.

Braun v. Wal-Mart Stores, Inc., 24 A.3d 875, 890-91 (Pa.Super.2011) (brackets in original; citations and quotation marks [1051]*1051omitted), affirmed, — Pa.-, 106 A.3d 656 (2014).

In reviewing a trial court’s denial of a motion for a new trial, the standard of review for an appellate court is as follows:
[I]t is well-established law that, absent a clear abuse of discretion by the trial court, appellate courts must not interfere with the trial court’s authority to grant or deny a new trial.
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Thus, when analyzing a decision by a trial court to grant or deny a new trial, the proper standard of review, ultimately, is whether the trial court abused its discretion.

Moreover, our review must be tailored to a well-settled, two-part analysis:

We must review the court’s alleged mistake and determine whether the court erred and, if so, whether the error resulted in prejudice necessitating a new trial.

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Cite This Page — Counsel Stack

Bluebook (online)
122 A.3d 1043, 2015 Pa. Super. 175, 2015 Pa. Super. LEXIS 473, 2015 WL 4940819, Counsel Stack Legal Research, https://law.counselstack.com/opinion/czimmer-v-janssen-pharmaceuticals-inc-pasuperct-2015.