Skip to main content

Lawsuit Claims Zostavax Vaccine Causes Shingles

Lawsuit Claims Zostavax Vaccine Causes Shingles

Lawsuit Claims Zostavax Vaccine Causes Shingles

Introduction

A California woman filed a lawsuit in the U.S. District Court for the Eastern District of Pennsylvania on June 14, against Merck & Co., alleging that it sold an unreasonably dangerous and ineffective shingles vaccine.

According to the complaint filed, the Zostavax shingles vaccine caused the woman to develop a painful, itchy, and blistering rash, as well as other dermatological issues, leading to the very condition it was designed to prevent. The lawsuit also claims the symptoms have resulted in physical limitations not present prior to using the vaccine. Zostavax introduced in 2006 is used for the prevention of shingles among older adults. It has been now replaced by the newer Shingrix vaccine. According to a study published in November 2018 in the BMJ, Shingrix is 85% more effective at preventing shingles than Zostavax.

Merck & Co. faces nearly 600 product liability claims, each raising similar allegations that the drugmaker failed to warn about the problems associated with the vaccine. Zostavax litigation is centralized before U.S. District Judge Harvey Bartle III in the Eastern District of Pennsylvania under MDL No. 2848.

Comments

Restricted HTML

  • Allowed HTML tags: <a href hreflang> <em> <strong> <cite> <blockquote cite> <code> <ul type> <ol start type> <li> <dl> <dt> <dd> <h2 id> <h3 id> <h4 id> <h5 id> <h6 id>
  • Lines and paragraphs break automatically.
  • Web page addresses and email addresses turn into links automatically.

Latest News

First Federal Bellwether Trial Set in Strattice Mesh Case

Categories: Hernia Mesh

Lawyers involved in federal Strattice hernia mesh litigation are scheduled to meet with the presiding judge in the U.S. District Court for the District of New Jersey to…

Tepezza Hearing Loss Trial Set for June 2026

Categories: Tepezza

The U.S. District Judge overseeing all federal Tepezza lawsuits has postponed the start of the first bellwether trial by 60 days.

This decision comes as attorneys…

FDA Moves to Restrict Dangerous 7-OH Opioid Products

Categories: Opioids

In a significant move to combat the ongoing opioid crisis, the U.S. Food and Drug Administration (FDA) has recommended a scheduling action under the Controlled Substances Act (CSA) to regulate certain products containing 7-hydroxymitragynine (7-…

✍️ FREE — 2,800 Pages Legal Process Outsourcing Trial!                 
No Contract. No Risk — Full Mass Tort + LPO Access, Free!

Only 10 Firms Accepted—Offer Ends August 31!