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Oxbryta Recall Lawsuits Claim Drug Manufacturer Knew About Fatality Risks for Years
Oxbryta Recall Lawsuits Claim Drug Manufacturer Knew About Fatality Risks for Years (Posted 4 days ago)

Although hundreds of Oxbryta fatalities were reported through the FDA's adverse event reporting system, lawsuits point out that it took Pfiizer years to issue an Oxbryta recall.

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BioZorb Lawsuit Indicates Recalled Tissue Marker Migrated After It Failed To Absorb, Resulting in Severe Pain and Surgical Removal
BioZorb Lawsuit Indicates Recalled Tissue Marker Migrated After It Failed To Absorb, Resulting in Severe Pain and Surgical Removal (Posted 5 days ago)

Days after the FDA announced a BioZorb recall, an Arkansas woman has filed a lawsuit, indicating that her BioZorb tissue marker migrated out of position, causing pain and disfigurement, instead of harmlessly absorbing into the body as advertised.

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Pulmonary Aspiration Warning Added to Ozempic, Wegovy, Mounjaro and Other GLP-1s Regarding Use Before Anesthesia or Deep Sedation
Pulmonary Aspiration Warning Added to Ozempic, Wegovy, Mounjaro and Other GLP-1s Regarding Use Before Anesthesia or Deep Sedation (Posted 5 days ago)

The FDA is requiring new label warnings for Ozempic, Wegovy, Mounjaro and all other GLP-1 drugs, indicating they may cause pulmonary aspiration during surgery.

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