Advertisement
Home Tags Food & Drug Administration

Tag: Food & Drug Administration

Nearly 2

FDA: Automated Endoscope Reprocessors Recalled

0
Custom Ultrasonics has history of violating federal rules for manufacturing and quality control
Cotellic (cobimetinib) in combination with another chemotherapy

FDA Approves Cotellic for Advanced Melanoma

0
For patients whose tumors express BRAF V600E or V600K mutations
A new treatment for HIV has been approved by the U.S. Food and Drug Administration. Genvoya -- a tablet containing elvitegravir

FDA Approves Genvoya to Treat HIV-1 Infection

0
Medication contains a new form of tenofovir not previously approved by the FDA
The melanoma drug Yervoy (ipilimumab) can now be used to reduce the risk of the recurrence after surgery

FDA Approves Expanded Use for Melanoma Drug

0
Yervoy can now be used after surgery to reduce risk of skin cancer returning
Imlygic (talimogene laherparepvec) has been approved by the U.S. Food and Drug Administration to treat melanoma lesions of the skin and lymph nodes.

FDA Approves Imlygic for Melanoma

0
Injectable drug designed to rupture and kill cancer cells
The U.S. Food and Drug Administration has approved Onivyde (irinotecan liposome injection) to be used in combination with fluorouracil and leucovorin in advanced pancreatic cancer.

FDA Approves Onivyde for Metastatic Pancreatic Cancer

0
To be used in combination with fluorouracil/leucovorin for advanced disease
The chemotherapy drug Yondelis (trabectedin) has been approved by the U.S. Food and Drug Administration to treat certain advanced or unresectable soft-tissue sarcomas.

FDA Approves Yondelis for Soft-Tissue Sarcoma

0
Drug sanctioned for liposarcoma or leiomyosarcoma
Coagadex (coagulation Factor X) has been approved by the U.S. Food and Drug Administration as the first coagulation factor replacement therapy for people with a rare blood disorder known as hereditary Factor X deficiency.

FDA Approves Coagadex for Rare Clotting Disorder

0
First coagulation therapy sanctioned for Factor X deficiency
Praxbind (idarucizumab) has been approved for use in patients who are taking the anticoagulant Pradaxa (dabigatran) when there is an urgent need to reverse Pradaxa's anticoagulant effects

FDA Approves Praxbind to Reverse Pradaxa’s Effect

0
Praxbind cleared for emergency use with Pradaxa when bleeding can't be controlled
The U.S. Food and Drug Administration on Monday expanded its approval for the Optune device to include newly diagnosed glioblastoma multiforme.

FDA Approves Optune Device for Newly Diagnosed Glioblastoma

0
Newly sanctioned to treat just-diagnosed patients, in combination with temozolomide