Zimmerman v. Novartis Pharmaceuticals Corp.

287 F.R.D. 357, 84 Fed. R. Serv. 3d 410, 2012 U.S. Dist. LEXIS 163865, 2012 WL 5816873
District Court, D. Maryland·Decided November 16, 2012·No. No. RWT 08cv2089·Published·Cited by 13 cases

Opinion

MEMORANDUM OPINION

ROGER W. TITUS, District Judge.

This pharmaceutical products liability lawsuit involves the drugs Aredia and Zometa, both of which were approved by the United States Food and Drag Administration (“FDA”) and are sold by defendant Novartis Pharmaceuticals Corporation (“Novartis”). On September 5, 2012, this Court entered an opinion and order granting a motion by Novartis to preclude any award of punitive damages. See ECF Nos. 166, 167. This matter is again before the Court on numerous other motions, including Defendant’s Renewed Motion for Summary Judgment. See ECF No. 174. The Court heard arguments with respect to all pending motions on November 1, 2012. As explained below, Defendant’s renewed motion will be granted, and all other pending motions will be denied as moot.

[359]*359Procedural History

On September 29, 2005, Phyllis Newman was first named as a plaintiff in a products liability diversity class action brought against Novartis in the United States District Court for the Middle District of Tennessee. She was also named in a second amended complaint filed on November 28, 2005. Ms. Newman died in 2007. Following the death of Ms. Newman and the dismissal without prejudice of the class action, the Plaintiff, Stacy Zimmerman, as personal representative of her estate, filed an individual products liability diversity action against Novartis in the United States District Court for the Middle District of Tennessee on December 5, 2007. Novartis is a Delaware corporation with its principal place of business in New Jersey. Ms. Newman was a resident of Maryland, as is her personal representative.

In her amended complaint, Plaintiff asserted strict liability and negligence claims against Novartis in connection with the manufacturing, distribution, promotion, testing, labeling and selling of Aredia and Zometa, two FDA approved bisphosphonate drugs which were approved for the treatment of patients with hypercalcemia of malignancy (a potentially fatal elevation of calcium in the blood), multiple myeloma, and breast cancer that has metastasized to bone. Ms. Newman, who was diagnosed with metastatic breast cancer to bone, was prescribed and received Aredia and Zometa in Maryland. As a result of her use of these drugs, she allegedly developed a jaw condition known as osteonecrosis (death of bone) of the jaw (“ONJ”).

On August 14, 2008, the United States District Court for the Middle District of Tennessee transferred the case under 28 U.S.C. § 1404 to this Court. On September 22, 2008, the Judicial Panel on Multidistrict Litigation issued a conditional transfer order transferring the case from this Court back to the Middle District of Tennessee for coordinated pretrial proceedings. On July 27, 2011, the Middle District of Tennessee advised the panel that coordinated pretrial proceedings had been completed and that the case should be remanded back to this Court.

Defendant first moved for summary judgment on May 19, 2011 while the case was still before the transferee judge in the multi-district litigation. See ECF No. 30. After remand from the transferee court and following a hearing held on October 31, 2011, that motion was denied by this Court as to the failure to warn claims on November 8, 2011. See ECF No. 93.

On September 18, 2012, after Plaintiff abandoned her previous theory of proximate causation [See Pl.’s Opp. to Mot. in Limine Regarding Dental Warnings (“Dental Warnings Opp.”), ECF No. 146, at 5] and introduced two new causation theories [See id. at 2-4, and Pl.’s Opp. to Mot. in Limine Regarding a Duty to Warn Doctors Other Than the Prescribing Physician (“Duty to Warn Opp.”), ECF No. 145, at 3], Defendant filed its Renewed Motion for Summary Judgment. See ECF No. 174. Plaintiff responded and also moved for leave to conduct additional discovery before responding. See ECF Nos. 186, 187. Defendant filed a reply, see ECF No. 189, and, as previously noted, the Court heard arguments on all pending motions on November 1, 2012. After the matter had been taken under advisement, and without obtaining leave of court to do so,1 the Plaintiff filed a Supplement to her Response in Opposition to Defendant’s Renewed Motion for Summary Judgment, to which Novartis responded. See ECF Nos. 197,198.

Background

Phyllis Newman was first diagnosed with breast cancer in 1987. See ECF No. 175 ¶ 1. Despite treatment, her cancer metastasized to her liver and bones by 1997. Id. at ¶ 2.

Dr. Marc Fisher, Ms. Newman’s periodontist, examined her in September 1997. See ECF No. 174, Ex. 2 ¶ 9; ECF No. 175 ¶¶ 14-16. He did not observe any problems with respect to her upper left third molar (tooth # 16, commonly known as a “wisdom tooth”), which was impacted (i.e., not erupted) at the [360]*360time. Id. In December 1997, Ms. Newman visited her general dentist, Dr. Danoff, who also did not observe any issues with tooth # 16, nor a need for any invasive dental procedures. See ECF No. 175, Ex. 13.

In January of 1998, Mrs. Newman’s oncologist, Dr. Frederick Smith, began prescribing her Aredia (later switched to Zometa in 2002) to prevent skeletal-related issues such as fractures and bone pain. See ECF No. 175 ¶ 4; ECF No. 193, Ex. 1 ¶¶3-4. Dr. Fisher evaluated Ms. Newman again in February 1998, and still observed no issues with impacted tooth # 16. See ECF No. 174, Ex. 2 ¶ 9; ECF No. 175 ¶ 14-16.

In June of 2001, Ms. Newman saw Dr. John Mennitt, an oral and maxillofacial surgeon, for problems that had arisen with tooth # 16, which had by then erupted likely due to Mrs. Newman’s age and the thinning of mucosa on that tooth. See ECF No. 175 ¶¶ 17, 18. The tooth was spontaneously exposed, was grossly decayed, and its extraction was unavoidable. Id. at ¶ 19. Dr. Mennitt recommended extraction which was carried out in July 2001. Id. at ¶¶ 17, 20. In August 2001, Dr. Mennitt observed a small sequest-rum, or a piece of exposed bone, at the extraction site. Id. at ¶26. This exposed bone represented the onset of Ms. Newman’s ONJ. Id. at ¶ 27.

In March of 2007, Ms. Newman died of metastatic breast cancer. Id. at ¶ 10.

DISCUSSION

I. Standard of Review on Summary Judgment

Summary judgment is proper if there are no issues of material fact and the moving party is entitled to judgment as a matter of law. Celotex Corp. v. Catrett, 477 U.S. 317, 322, 106 S.Ct. 2548, 91 L.Ed.2d 265 (1986); Francis v. Booz, Allen & Hamilton, Inc., 452 F.3d 299, 302 (4th Cir.2006). A material fact is one that “might affect the outcome of the suit under the governing law.” Spriggs v. Diamond Auto Glass, 242 F.3d 179, 183 (4th Cir.2001)(quoting Anderson v. Liberty Lobby, 477 U.S. 242, 248, 106 S.Ct. 2505, 91 L.Ed.2d 202 (1986)).

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Zimmerman v. Novartis Pharmaceuticals Corp., 287 F.R.D. 357, 84 Fed. R. Serv. 3d 410, 2012 U.S. Dist. LEXIS 163865, 2012 WL 5816873 (D. Md. 2012).

287 F.R.D. 357 (Zimmerman v. Novartis Pharmaceuticals Corp.) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

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