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The company secured final approval from the US Food and Drug Administration (FDA) for its abbreviated new drug application (ANDA) for the product, which is indicated as monotherapy,

The labeling update includes dosing guidelines as well as safety and efficacy findings for the use of VELCADE as a single agent or VELCADE in combination with dexamethasone

Data Highlights BIOD-531 was associated with superior glucose control compared to Humalog Mix 75/25 throughout the day of observation. BIOD-531 was also associated with superior glucose control compared

Mosquitos can easily and efficiently transmit this virus to humans causing high fever, severe muscle/joint pain, headache, fatigue and rash. While there is currently no FDA-approved vaccine to

The administration of particulate matter, if present in an intravenous drug, poses a potential safety risk to patients such as a thromboembolism or a life-threatening pulmonary embolism. Other

Under the agreement, Fred’s and Cardinal Health will establish a mutually beneficial strategic alliance designed to support Fred’s key initiative of rapid pharmacy growth, and build on a

The approval follows after a request from the Liberian Government on 8 August to send sample doses of experimental Serum for use on two Liberian doctors who are

The fresh round of charges was said to be seen by Reuters news agency in an anonymous email sent to chief executive Andrew Witty and GSK audit committee

Conducted on 15 healthy volunteers at Linear Clinical Research’s facility in Perth, Australia, the study validated additional pharmacokinetic parameters associated with the safety and elimination profile that remained