Labzda v. Purdue Pharma L.P.

292 F. Supp. 2d 1346, 2003 U.S. Dist. LEXIS 23991, 2003 WL 22908816
CourtDistrict Court, S.D. Florida
DecidedSeptember 23, 2003
Docket018726CIV
StatusPublished
Cited by3 cases

This text of 292 F. Supp. 2d 1346 (Labzda v. Purdue Pharma L.P.) is published on Counsel Stack Legal Research, covering District Court, S.D. Florida primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Labzda v. Purdue Pharma L.P., 292 F. Supp. 2d 1346, 2003 U.S. Dist. LEXIS 23991, 2003 WL 22908816 (S.D. Fla. 2003).

Opinion

FINAL JUDGMENT

MARRA, District Judge.

THIS CAUSE is before the Court upon the Defendants, Purdue Pharma L.P., Purdue Pharma, Inc., and the Purdue Frederick Company’s Motion for Summary Judgment [DE 106], the Report and Recommendation [DE 187] of Magistrate Judge Lurana S. Snow, filed September 8, 2003, and the Joint Stipulation for Entry of Final Judgment [filed September 19, 2003]. The Court has carefully considered the record, and is otherwise fully advised in the premises.

As described in the Report and Recommendation, the only parties remaining in this case are the Plaintiffs and the Purdue Defendants. The Report of Judge Snow recommended that the Defendants’ Motion for Summary Judgment be granted. Pursuant to the Court’s review of the Report and Recommendation and the parties’ stipulation, the Court adopts the Report and Recommendation.

Accordingly, it is ORDERED AND ADJUDGED as follows:

1. The Magistrate Judge’s Report and Recommendation [DE 187] is hereby ADOPTED;

2. Defendants, Purdue Pharma L.P., Purdue Pharma,. Inc., and the Purdue Frederick Company’s Motion for Sum *1348 mary Judgment [DE 106] is hereby GRANTED;

3. This action against Defendants Purdue Pharma L.P., Purdue Pharma, Inc., and the Purdue Frederick Company is hereby DISMISSED WITH PREJUDICE;

4. Judgment is hereby entered on behalf of Defendants Purdue Pharma L.P., Purdue Pharma, Inc., and the Purdue Frederick Company, and against the Plaintiffs, William Labzda and Carol Jo Labzda and Plaintiffs shall take nothing from Defendants in this action;

5. Each party shall bear their own fees and costs;

6. The Order sealing the Report and Recommendation [DE 189] is hereby VACATED;

7. Any other pending motions are denied as moot;

8. The Clerk may close this case.

REPORT AND RECOMMENDATION

SNOW, United States District Judge.

THIS CAUSE is before the Court on the Defendant Purdue’s Motion for Summary Judgment (Docket Entry 106), which was referred to United States Magistrate Judge Lurana S. Snow for report and recommendation.

I. PROCEDURAL HISTORY

The complaint was filed in July 2001 in the Fifteenth Judicial Circuit in and for Palm Beach County, Florida, alleging violation of Florida’s Deceptive and Unfair Trade Practices Act, negligence and public nuisance related to the accidental death of Michael Labzda related to his misuse of the drug OxyContin. The complaint named as defendants Purdue Pharma L.P., Purdue Pharma Inc., The Purdue Frederick Company, Abbott Laboratories, Abbott Laboratories, Inc., Walgreen Co. d/b/a Walgreens Family Physician P.A. and Denis Deonarine, M.D.

The defendants removed the case to federal court based on diversity of jurisdiction (Walgreen filed a consent to the removal) and federal question jurisdiction related to the federal regulatory scheme for prescription drugs. All of the defendants filed answers, except Walgreen, which filed a motion to dismiss for failure to state a claim (Docket Entry 9). On October 31, 2001, the Court adopted the stipulation of the parties and dismissed the claim against Dr. Deonarine. On November 26, the Court entered the stipulated dismissal of Walgreen’s Family Physician P.A.

Thereafter, Purdue Pharma L.P. filed a motion for a judgment on the pleadings (DE 43) and the plaintiff filed a motion to dismiss Count I as to all defendants (DE 50). Abbott Laboratories filed a motion for summary judgment (DE 66), which was granted by default (DE 78). The Court adopted the stipulation of dismissal of the Walgreen Company (DE 87) and the stipulation of dismissal for Abbott Laboratories and Abbott Laboratories, Inc. (DE 100).

On December 2, 2002, the plaintiffs sought leave to file an amended complaint, which the Court granted (DE 117). The amended complaint, with a single count of wrongful death, named as defendants Purdue Pharma, L.P., Purdue Pharma, Inc., and The Purdue Frederick Company. The plaintiffs alleged that their adult son, Michael Labzda, died as a result of misusing OxyContin prescribed by Dr. Denis Deonarine. The amended complaint alleged that the Purdue defendants knew *1349 that Dr. Deonarine, without sufficient examination, over-prescribed OxyContin to patients; but the defendants did not attempt to curtail the inappropriate prescriptions, ignoring the potential for abuse of their product. The plaintiffs contend that this constituted a breach of the duty of care in the marketing and distribution of the product.

Mediation in February 2002 resulted in an impasse (DE 105). The Purdue defendants subsequently filed the instant motion for summary judgment, which is fully briefed and is ripe for consideration.

II. MATERIAL FACTS NOT AT ISSUE

The defendants provided a detailed list of material facts regarding the product and its approved use, how it was prescribed for Michael Labzda and the manner in which he used the product on the night before his death. The plaintiffs submitted a responsive statement of material facts, none of which contradict the material facts in the defendants’ statement, but instead focus on the actions of the physician who issued the prescriptions to Michael Labzda, and the marketing efforts the defendants directed toward that physician. The defendants’ reply, noting that the plaintiffs did not dispute any of the facts proffered by the defendants, asserts that they are entitled to a judgment as a matter of law.

The defendants’ statement reveals that in December 1995, the Food and Drug Administration approved Purdue’s sale of OxyContin, a controlled-release form of ox-ycodone. (DE 109, Exhibit 5 ¶ 3) While oxycodone has been approved for prescription use for more than 60 years, Purdue’s product was unique in its controlled-release design. (Id. at ¶ 5) OxyContin is available by prescription only. (Id. at ¶ 4)

Michael Labzda obtained a prescription for OxyContin from Dr. Denis Deonarine on July 17, 2000. (DE 109, Exhibit 15, medical records of Dr. Deonarine, MED 00053-54 and 00061-62) Michael Labzda filled out a New Patient Information for stating that he had a history of back pain. (Id. at MED 00054) He told Dr. Deonarine that he suffered lower back pain from a tractor accident. (Id. at MED 00061). Dr. Deonarine diagnosed chronic back pain and anxiety and/or panic attacks and issued a thirty-day prescription for OxyCon-tin, Oxy IR 5 and Xanax. (Id. at MED 00061-62) Michael Labzda returned to Dr. Deonarine on August 17, 2000, and November 7, 2000, each time receiving a 30-day prescription of OxyContin and Xanax. (Id. at MED 00063-75). On February 6, 2001, Michael Labzda again visited Dr. Deonarine and was required to fill out and sign a Pain Management Agreement in which he agreed not to use illegal controlled substances; not to share, trade or sell his medication; not to attempt to obtain controlled substances from any other doctor, and not to use the medication at a rate greater than the prescribed rate. (Id. at MED 00072-73).

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Bluebook (online)
292 F. Supp. 2d 1346, 2003 U.S. Dist. LEXIS 23991, 2003 WL 22908816, Counsel Stack Legal Research, https://law.counselstack.com/opinion/labzda-v-purdue-pharma-lp-flsd-2003.