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Jessica Hoerman

Stockert 3T Heater-Cooler Linked to Infection

Stockert 3T Heater-Cooler lawsuits are being filed on behalf of individuals diagnosed with a serious infection, non-tuberculous mycobacteria (NTM), as a result of the use of a heater-cooler system during open-chest surgery.

Jessica Hoerman

Homeopathic Teething Tablets Causing Seizures in Infants?

FDA records from 2012 to the present day tell the sad story of seven years of belladonna poisoning that could have been prevented

Jessica Hoerman

Permanent Hair Loss Not Warned about With Taxotere Use

Sanofi-Aventis obtained billions of dollars in increased revenues at the expense of unwary cancer victims simply hoping to survive their condition and return to a normal life.

Steven Davis

$300 Million Benicar Settlement Reached

A $300 million Benicar settlement was reached. For those who believe their gastrointestinal illness was caused by a Benicar prescription, contact a lawyer.

Tor Hoerman

Calling Hyland’s Teething Tablets a “serious health risk” FDA Finally Drops Hammer

A stunning FDA recall letter dated April 7, 2017 to Jay Borneman, CEO of Hyland’s, lays out shockingly strong warnings and statements about Hyland’s dangerous teething products. The FDA stated a recall was necessary because “there is a reasonable probability that the use [of teething tablets]…will cause serious adverse event health consequences or death.”

Jacob Plattenberger

FDA Raises Concern About Breast Implants and Cancer

As of February 1st, 2017, the FDA has received 359 reports of a rare type of breast cancer linked to breast implants. The FDA has confirmed that a malignancy of the immune system associated with breast implants has resulted in […]

Tor Hoerman

Hyland’s Homeopathic Teething Tablets Ingredient, Toxic Belladonna, Puts Your Child at an Unnecessary Risk of Injury/Death – CEO Doesn’t Care

What would you do if you were the owner and CEO of a company whose product had been linked by the FDA to the sudden deaths of nearly a dozen infants? Warn the public? Pull the product from the shelves? […]

Chad Finley

FDA Warns Doctors About “Absorb” Dissolving Heart Stent

FDA is warning medical providers that Absorb dissolving stents may lead to more cardiac injuries than other non-dissolving stents.

Chad Finley

Deregulation and Budget Cuts Likely to Lead to Increased Adverse Event Reporting in Pharmaceutical Industry

With deregulation of FDA oversight, cuts in funding to institutions conducting government research and overview, and the potential for essentially the privatization of the FDA because of increased industry funding, it is likely we will see an increase in injuries and thus adverse event reports

Chad Finley

Should I Report A Drug Injury or Drug Side Effect?

For all of these reasons, it is imperative that consumers understand that the need to report drug injuries or side effects is great. Reports are a critical way the FDA can detect injuries or side effects early and prevent it from unnecessarily happening to others