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Personal Injury
Product Liability
Pharmaceutical

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

Anthony J. Mohr

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)

Aton Arbisser


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


#98047

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