Haimowitz v. Novartis Pharmaceuticals Corp.

148 F. Supp. 3d 327, 2015 U.S. Dist. LEXIS 166418, 2015 WL 8675349
CourtDistrict Court, S.D. New York
DecidedDecember 11, 2015
DocketNo. 09 Civ. 10068 (JFK)
StatusPublished
Cited by1 cases

This text of 148 F. Supp. 3d 327 (Haimowitz v. Novartis Pharmaceuticals Corp.) is published on Counsel Stack Legal Research, covering District Court, S.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Haimowitz v. Novartis Pharmaceuticals Corp., 148 F. Supp. 3d 327, 2015 U.S. Dist. LEXIS 166418, 2015 WL 8675349 (S.D.N.Y. 2015).

Opinion

OPINION & ORDER

John F. Keenan, United States District Judge:

Before the Court is Defendant Novartis Pharmaceuticals Corporation’s motion for summary judgment pursuant to Federal Rule of Civil Procedure 56. Defendant seeks summary judgment on the ground that Plaintiff Beryl Haimowitz’s tort and warranty claims are untimely under New York law.1 For the reasons that follow, the motion is granted and summary judgment is entered in Defendant’s favor.

I. Background

The following facts are taken from the record following discovery. This case concerns allegations that Plaintiffs use of the drug Aredia caused her to develop bis-phosphonate-related osteonecrosis of the jaw (referred to as “ONJ”). Bisphosphonate-related ONJ is defined as exposed bone in the jaw of more than eight-weeks duration in a patient who has undergone bisphosphonate treatment and who has not received radiation to the jaw. (ECF No. 21, Def.’s Statement of Undisputed Facts (“SUF”) ¶¶ 5-8.) Aredia is a Food and Drug Administration-approved bis-phosphonate medication sold by Defendant Novartis Pharmaceutical Corporation (“Novartis”), which is prescribed for the prevention of bone damage in patients with multiple myeloma or cancer. (ECF No. 26, Def.’s Mem. at 4.)

Plaintiff was living in New York in December 1995 when she was diagnosed with multiple myeloma. As a result, Ms. Hai-mowitz’s oncologist at the time — Dr. Ivan K. Rothman — prescribed Aredia as part of her treatment. Medical records from Dr. Rothman’s practice show that Plaintiff received Aredia on a monthly basis from December 29, 1995 through May 28, 1997 and then from August 8, 1997 through March 29, 2002.2

In July 1997, while her treatment with Aredia was ongoing, Ms. Haimowitz underwent oral surgery to extract a lower left molar. Healing was normal until November 18, 1997, when Plaintiff began to complain of swelling, pain, and exposed bone at the extraction site. Thereafter, from.November 1997 through August 2002, Plaintiff repeatedly sought treatment for symptoms including infections and exposed bone in her jaw. (Pls.’ Resp. to SUF ¶¶ 14-26.) These symptoms became serious enough that Ms. Haimowitz underwent surgery for the “resection of her mandible” in August 2002. (See id. ¶¶ 20, 27).

Plaintiff continued to live in New York throughout the time that she was treated with Aredia. (SUF ¶¶ 2, 35-38.) In June 2002, however, she moved from New York to Maryland. Shortly thereafter, her new oncologist — Dr. Flavio Kruter — discontinued her bisphosphonate treatment. Plaintiffs medical records from the time indicate that Ms. Haimowitz’s jaw problems continued over the following years and that at- least some of her doctors believed [330]*330that these problems were due to bisphos-phonate-related ONJ. (SUF ¶¶ 26-30.)

Plaintiff filed this action on December 8, 2009. The complaint asserts common law claims for tort and breach of warranty. Following Ms. Haimowitz’s death due to unrelated causes in August 2012, her children — Aaron Haimowitz and Caryn Ler-man — were substituted as plaintiffs in this case. (See EOF No. 8-7, Order dated Jan. 15,2014.) The present motion for summary judgment was filed by Novartis on November 2, 2015.

II. Discussion

A. Legal Standard

Summary judgment is warranted when “there is no genuine' issue as to any material fact and the movant is entitled to judgment as a matter of law.” Fed. R. Civ. P. 56(a). A dispute regarding a material fact is genuine “if the evidence is such that a reasonable jury could return a verdict for the non moving party.” Anderson v. Liberty Lobby, Inc., 477 U.S. 242, 248, 106 S.Ct. 2505, 91 L.Ed.2d 202 (1986). “If, as to the issue on which summary judgment is sought, there is any evidence in the record from which a reasonable inference could be drawn in favor of the opposing party, summary judgment is improper.” Gummo v. Village of Depew, 75 F.3d 98, 107 (2d Cir.1996).

Where a defendant requests summary judgment on the ground that the statute of limitations ¡on plaintiffs claim has run, the defendant bears the burden of proving that the particular limitation period has expired. Vincent v. Money Store, 915 F.Supp.2d 553, 562 (S.D.N.Y.2013); see also Celotex Corp. v. Catrett, 477 U.S. 317, 322-23, 106 S.Ct. 2548, 91 L.Ed.2d 265 (1986)(noting that the party seeking summary judgment bears the burden of demonstrating the absence of any genuine factual dispute). Once that burden has been met, however, it falls to the plaintiff to prove that the statute of limitations has been tolled. Id.

B. Analysis

1. Choice of Law

As a prehminary matter, the parties dispute what state’s law controls the statutes of limitations in this case. Plaintiff contends that Maryland law governs the limitations period for both sets of claims on the ground that she resided in Maryland when she allegedly discovered that Aredia was the cause of her injuries and filed this action against Novartis. By comparison, Novartis argues that New York’s statute of limitations applies to Plaintiffs claims, because Ms. Haimowitz resided in New York at the time that she received all of her Aredia infusions and was in New York when she first developed ONJ-related symptoms.

It is well-settled that where, as here, federal jurisdiction rests upon diversity of citizenship, the district court must apply the forum state’s statute of limitations provisions.3 See Klaxon Co. v. Stentor Elec. Mfg. Co., 313 U.S. 487, 496, 61 S.Ct. 1020, 85 L.Ed. 1477 (1941); Vincent, 915 F.Supp.2d at 562. Where a nonresident plaintiff brings an action in New York— the forum state in this case — New York law provides for different limitations provisions depending on where the underlying cause of action accrued. Where a nonresident plaintiff asserts a claim that accrued in New York, then Néw York law controls the applicable limitations period. See, e.g., [331]*331Martin v. Julius Dierck Equip. Co., 52 A.D.2d 463, 465, 384 N.Y.S.2d 479 (N.Y.App.Div.1976) (addressing claims by a nonresident and reasoning “that since the warranty claims accrued in this State, New York’s own fouhyear Statute of Limitations applied” (internal citation omitted)). Alternatively, where a nonresident plaintiff files suit based on a cause of action that accrued outside New York, New York’s borrowing statute instructs courts to apply the shorter statute of limitations period, as well as all applicable tolling provisions, provided by either New York or the state where the cause of action accrued. N.Y. C.P.L.R. § 202; see Cantor Fitzgerald Inc. v. Lutnick,

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148 F. Supp. 3d 327, 2015 U.S. Dist. LEXIS 166418, 2015 WL 8675349, Counsel Stack Legal Research, https://law.counselstack.com/opinion/haimowitz-v-novartis-pharmaceuticals-corp-nysd-2015.