Pearl O'Neill v. Novartis Consumer Health Inc.
Published: Sep. 8, 2004 | Result Date: Feb. 6, 2004 | Filing Date: Jan. 1, 1900 |Case number: 01CC070503 Verdict – $0
Judge
Court
L.A. Superior Central West
Attorneys
Plaintiff
Ramon Rossi Lopez
(Lopez McHugh LLP)
Mark P. Robinson Jr.
(Robinson Calcagnie Inc.)
Defendant
Jan E. Dodd
(Shook Hardy & Bacon LLP)
Experts
Plaintiff
Raymond Lake
(medical)
Jerome Avorn
(medical)
Hugh McIntyre
(medical)
Henry Pribham
(medical)
Mark Fisher
(medical)
James C. Parker
(Hugo Parker LLP)
(technical)
Douglas E. Harrington
(medical)
Susan Hurst
(medical)
Defendant
Donald Goldman
(medical)
Gerald Faich
(technical)
Mark Alberts
(medical)
Paul Bowie Watkins Jr.
(medical)
Facts
In April 1995, plaintiff Pearl O'Neill, 35, took a single dose of Tavist-D for a sinus headache. The medicine contained phenylpropanolamine (PPA). After taking the medicine, the plaintiff suffered an intracerebral hemorrhage. Five years later, the Food and Drug Administration requested that all drug manufacturers remove PPA from their over-the-counter products. A study had shown that PPA increases the risk of stroke.
Injuries
The plaintiff's hemorrhage led to psychological and cognitive difficulties that made her unable to continue her work as a legal secretary.
Deliberation
2.5 days
Poll
9-3 (design defect), 10-2 (failure to warn), 10-2 (fraud by concealment)
Length
3.5 months
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