LAKE ZURICH, Ill.--(BUSINESS WIRE)--Fresenius Kabi announced today the immediate availability in the United States of Phenylephrine Hydrochloride Injection, USP. Fresenius Kabi Phenylephrine ...
To date, the Company has not received any reports of adverse events related to this recall. Leiters Health is voluntarily recalling 33 lots of vancomycin intravenous (IV) bags, phenylephrine IV bags, ...
A drug used to bring a person’s blood pressure back up after anesthesia is being recalled because it may not be sterile. Sagent Pharmaceuticals announced its nationwide recall of three lots of ...
A non-integral crimped vial overseal may result in a non-sterile product. Sagent Pharmaceuticals is recalling 3 lots of Phenylephrine Hydrochloride Injection, USP (10mg/mL) due to potentially loose ...
January 5, 2024 – Englewood, Colorado, Leiters Health is voluntarily recalling 33 lots of products listed below to the user level. The recalled batches of vancomycin IV bags, phenylephrine IV bags, ...
To describe the use of intracameral phenylephrine to prevent the floppy iris syndrome seen in patients who are on the drug tamsulosin for benign prostatic hypertrophy, during cataract surgery. There ...
To analyse the relationship between the results of the phenylephrine test and postoperative eyelid droop in transcutaneous aponeurotic repair using epinephrine-containing local anaesthetic for ...