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Jack v. Glaxo Wellcome, Inc.

Citations: 239 F. Supp. 2d 1308; 2002 WL 31936801Docket: CIV.A.1:99CV2697CAP

Court: District Court, N.D. Georgia; August 23, 2002; Federal District Court

Narrative Opinion Summary

In the case of Ida Jack v. Glaxo Wellcome Inc., the court addressed several procedural and substantive motions related to the plaintiff's claims of injuries caused by the drug Zyban, manufactured by Glaxo Wellcome. The plaintiff alleged that Zyban, containing bupropion, led to her development of panic attacks and other medical conditions. The case was removed to federal court, where Glaxo sought summary judgment and moved to exclude key evidence, particularly expert testimonies. The court applied the Daubert standards and Rule 702 to assess the admissibility of expert testimony, ultimately excluding the testimonies of Dr. Richtand and others due to insufficient reliability and methodology. The court also applied the learned intermediary doctrine, emphasizing that the duty to warn of drug risks lies with the prescribing physician. As a result, the court granted summary judgment in favor of Glaxo, concluding that the plaintiff failed to establish general causation. The decision was influenced by the exclusion of expert evidence, lack of genuine disputes over material facts, and the application of relevant legal principles, including the learned intermediary doctrine, which collectively negated the plaintiff's claims of negligence, strict liability, and breach of implied warranty.

Legal Issues Addressed

Admissibility of Expert Testimony under Daubert and Rule 702

Application: The court excluded expert testimony from Dr. Richtand and others, finding their methods unreliable and not meeting the standards required for admissibility under Daubert and Rule 702.

Reasoning: The Daubert criteria apply to all experts, requiring an examination of the expert's credentials and the reliability of their methodology.

Exceeding Local Page Limit in Briefs

Application: Both parties' motions to exceed the local page limit for their briefs were granted, allowing them to present extended arguments.

Reasoning: The plaintiff's motion to exceed the local page limit was granted, as was the defendant's similar motion.

Learned Intermediary Doctrine in Georgia

Application: The court applied the learned intermediary doctrine, emphasizing the manufacturer's duty to warn the prescribing physician, not the patient, limiting the defendant's liability.

Reasoning: Additionally, under the learned intermediary doctrine in Georgia, the responsibility to warn patients of drug risks lies with the physician, not the manufacturer.

Motions in Limine and Evidentiary Exclusions

Application: The court ruled on various motions in limine, excluding certain expert testimonies while leaving others moot, which impacted the summary judgment decision.

Reasoning: The defendant's motions in limine concerning Dr. Richtand, Dr. Tiedt, Dr. Rand, and Dr. Oren were granted in part and denied as moot in part.

Summary Judgment Standards under Rule 56(c)

Application: The court granted summary judgment to the defendant, finding no genuine issue of material fact related to the causation claims presented by the plaintiff.

Reasoning: Summary judgment is governed by Rule 56(c) of the Federal Rules of Civil Procedure, allowing for judgment when there is no genuine dispute over material facts.