Salix announces FDA approval of Xifaxan 550 mg for the treatment of IBS-D (irritable bowel syndrome with diarrhoea)

Valeant Pharmaceuticals International, Inc. announced that its wholly owned subsidiary, Salix Pharmaceuticals, Inc., has received approval from the U.S. Food and Drug Administration (FDA) ...

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FDA approves two therapies to treat IBS-D

The U.S. Food and Drug Administration today approved Viberzi (eluxadoline) and Xifaxan (rifaximin), two new treatments, manufactured by two different ...

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Alcon receives FDA approval of Pazeo solution for ocular allergy itch relief

Alcon, the global leader in eye care and a division of Novartis, has received approval from the U.S. Food and ...

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Bristol-Myers Squibb Statement about asunaprevir in the U.S.

Given the rapidly evolving hepatitis C (HCV) treatment landscape in the U.S., Bristol-Myers Squibb has decided that it will not pursue ...

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FDA approves new antibacterial drug Avycaz

The U.S. Food and Drug Administration today approved Avycaz (ceftazidime-avibactam), a new antibacterial drug product, to treat adults with complicated ...

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FDA approves Akynzeo for nausea and vomiting associated with cancer chemotherapy

The U.S. Food and Drug Administration today approved Akynzeo (netupitant and palonosetron) to treat nausea and vomiting in patients undergoing ...

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FDA approves Esbriet to treat idiopathic pulmonary fibrosis

The U.S. Food and Drug Administration today approved Esbriet (pirfenidone) for the treatment of idiopathic pulmonary fibrosis (IPF). ...

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InterMune announces resubmission of NDA for pirfenidone for the treatment of patients with IPF

InterMune, Inc. today announced that it has resubmitted its pirfenidone New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) in ...

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Runaway drug prices

A drug to treat abnormal heart rhythms can cost about $200 on one day and more than $1,300 the next. ...

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Cyramza now approved in the U.S. for use with FOLFIRI in second-line treatment of metastatic colorectal cancer

5 November 2014 - Eli Lilly and Company has received its fourth U.S. FDA approval for Cyramza (ramucirumab).  ...

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Amgen submits supplemental new drug application for Kyprolis (carfilzomib) in relapsed multiple myeloma

Amgen today announced the submission of a supplemental New Drug Application (sNDA) to the U.S. Food and Drug Administration (FDA) for Kyprolis (carfilzomib) ...

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Sunovion Pharmaceuticals Inc. announces FDA acceptance for review of supplemental New Drug Application for the use of Aptiom (eslicarbazepine acetate) as monotherapy treatment for partial-onset seizures

Sunovion Pharmaceuticals Inc. (Sunovion) announced today the U.S. Food and Drug Administration (FDA) has accepted for review a supplemental New ...

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FDA approves Baxter's Rixubis [coagulation factor IX (recombinant)] for treatment of children with hemophilia B

Baxter International Inc. today announced that the United States Food and Drug Administration (FDA) has approved Rixubis [Coagulation Factor IX (Recombinant)] for ...

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FDA approves first therapy for high-risk neuroblastoma

The U.S. Food and Drug Administration today approved Unituxin (dinutuximab) as part of first-line therapy for pediatric patients with high-risk ...

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Viagra slows the spread of malaria, study finds

The little blue pill that gives men more oomph in the bedroom has an unexpected benefit - it can slow the ...

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