Lawsuits Over Fen-Phen Side Effects Years Later Allowed to Proceed

A federal judge has rejected an attempt by Pfizer to cut-off new lawsuits over fen-phen, which continue to be brought by individuals who indicate that they developed persistent pulmonary hypertension (PPH) from side effects of the weight-loss drug years after it was recalled from the market.  

In an order issued August 30, U.S. District Judge Harvey Bartle III determined that expert testimony introduced by plaintiffs, who allege that fen-phen side effects can cause serious lung problems nine or more years after last use, relies on reasonable medical studies and case reports, although a jury will still have to determine whether that evidence is sufficient.

Fen-phen was a popular diet drug that involved a combination of phentermine and fenfuramine, which was marketed as Pondimin. Fenfuramine was recalled in September 1997, after side effects were shown to cause life-threatening pulmonary hypertension and heart valve problems

Did You Know?

AT&T Data Breach Impacts Millions of Customers

More than 73 million customers of AT&T may have had their names, addresses, phone numbers, Social Security numbers and other information released on the dark web due to a massive AT&T data breach. Lawsuits are being pursued to obtain financial compensation.

Learn More

The decision came in response to a motion filed by Pfizer’s Wyeth subsidiary to dismiss lawsuits filed by two women, Valarie Farmer and Jamie Cheek, who allege that they developed PPH from the recalled diet drug. Cheek alleged that she took the weight-loss drugs for approximately one year ending in late-1996, and filed her lawsuit in January 2011 after that she developed PPH. Farmer used the diet drug Pondimin for approximately three months in 1997, and was diagnosed with PPH in June 2011.

Pfizer had argued that the fen-phen PPH lawsuits should be dismissed because there is a lack of sound medical evidence linking the medication to the disease occurring nine or more years after last use.

In most cases, state-based statutes of limitations limit the amount of time a plaintiff can bring a product liability lawsuit against the manufacturer of a dangerous medication. However, under the latency argument, which indicates that signs of PPH may not appear for years after last use of fen-phen, some plaintiffs are able to argue that they did not discover they were injured until recently.

Judge Bartle is overseeing about 30 PPH fen-phen lawsuits in federal court in Philadelphia, and there are others that have been filed in state court in Pennsytlvania, which Pfizer is also reportedly trying to have dismissed. Pfizer and Wyeth have reportedly paid out an estimated $21 billion in fen-phen settlements since it was removed from the market.

0 Comments

Share Your Comments

I authorize the above comments be posted on this page*

Want your comments reviewed by a lawyer?

To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.

NOTE: Providing information for review by an attorney does not form an attorney-client relationship.

This field is for validation purposes and should be left unchanged.

More Top Stories

Novo Nordisk Fails To Warn About Risk of Gastroparesis from Wegovy, Lawsuit Alleges
Novo Nordisk Fails To Warn About Risk of Gastroparesis from Wegovy, Lawsuit Alleges (Posted 3 days ago)

A Wegovy gastroparesis lawsuit filed by a Pennsylvania couple accuses the manufacturer, Novo Nordisk, of failing to provide adequate warnings about the true risks of the injectable weight loss drug.

Lawyers
Lawyers "Optimistic" Suboxone Tolling Agreement Will Be Reached For Tooth Decay Lawsuits (Posted 3 days ago)

Plaintiffs and defendants involved in Suboxone tooth decay lawsuits say they are close to a deal that would allow the filing of federal complaints after some state statue of limitation laws would have disqualified plaintiffs from filing.

Lawsuit Indicates Tepezza Hearing Impairment Warnings Were Delayed By Horizon Therapeutics, Disregarding Safety of Users
Lawsuit Indicates Tepezza Hearing Impairment Warnings Were Delayed By Horizon Therapeutics, Disregarding Safety of Users (Posted 4 days ago)

New Jersey man indicates he has been left with permanent hearing impairment from Tepezza, alleging that Horizon Therapeutics failed to instruct doctors about the importance of conducting hearing tests on patients using the thyroid eye disease drug.