Tag Archives: Hydromorphone

Medtronic SynchroMed II Pump Lawsuit Filed Over Malfunctions That Resulted in Drug Overdoses

September 24, 2020 By: Irvin Jackson
Injecting Opioids Increases The Risk Of Bacterial Heart Infections: Study

January 31, 2019 By: Martha Garcia
Nationwide PharMEDium Compounded Opioid Drug Recall Issued Over Sterility Concerns

January 04, 2018 By: Irvin Jackson
Random Opioid Testing Required For Pilots, Train Engineers, DOT Announces

November 10, 2017 By: Martha Garcia
Drug Makers Often Fail To Tell FDA, Research Subjects, About Adverse Events in Timely Manner: Studies

July 31, 2015 By: Irvin Jackson
Hospira Medical Device Manufacturing Problems Get FDA Warning

February 14, 2013 By: Irvin Jackson
Problems at Hospira Infusion Pump Plant Result in FDA Warning

August 29, 2012 By: Irvin Jackson
Hydromorphone Recall Issued Due to Overdose Risk

August 21, 2012 By: Irvin Jackson
Hospira Hydromorphone Hydrochloride Recall Due to Overdose Risk

May 14, 2012 By: Staff Writers
Novartis Recalls Excederin, Bufferin, NoDoz, Gas-X, Other Drugs

January 10, 2012 By: Staff Writers

Lawsuit Alleges Suboxone Caused Dental Damage, Erosion and Tooth Decay (Posted 4 days ago)

Kentucky man has filed a lawsuit against Suboxone manufacturers, indicating the opioid treatment film strips were known for years to cause the kind of permanent tooth damage he suffered, long before warning labels were added by the drug manufacturer.

Master Complaint Outlines Allegations in Ozempic, Wegovy, Mounjaro Lawsuits in MDL (Posted 7 days ago)

Plaintiffs pursuing GLP-1 injury lawsuits have filed a Master Complaint outlining common allegations being pursued against Novo Nordisk and Eli Lilly over their diabetes and weight loss drugs, including Ozempic, Wegovy, Mounjaro and others.

Judge Declines To Extend Bard PowerPort Lawsuit Deadlines Under Discovery Schedule (Posted 9 days ago)

As parties prepare for early Bard PowerPort lawsuit bellwether trials, the court rejected a request to extend discovery deadlines by two months.

Tag Archives: Hydromorphone

Medtronic SynchroMed II Pump Lawsuit Filed Over Malfunctions That Resulted in Drug Overdoses

Injecting Opioids Increases The Risk Of Bacterial Heart Infections: Study

Nationwide PharMEDium Compounded Opioid Drug Recall Issued Over Sterility Concerns

Random Opioid Testing Required For Pilots, Train Engineers, DOT Announces

Drug Makers Often Fail To Tell FDA, Research Subjects, About Adverse Events in Timely Manner: Studies

Hospira Medical Device Manufacturing Problems Get FDA Warning

Problems at Hospira Infusion Pump Plant Result in FDA Warning

Hydromorphone Recall Issued Due to Overdose Risk

Hospira Hydromorphone Hydrochloride Recall Due to Overdose Risk

Novartis Recalls Excederin, Bufferin, NoDoz, Gas-X, Other Drugs

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