Content about Pfizer

August 29, 2010

Pharmacists' role has significantly changed, with more than 90% of pharmacists believing they are key...

August 26, 2010

The Food and Drug Administration has approved a generic treatment for hypertension and liver cirrhosis...

HAUPPAUGE, N.Y. The Food and Drug Administration has approved a generic treatment for hypertension and liver cirrhosis made by Amneal Pharmaceuticals, Amneal said Thursday.

 

The FDA approved Amneal’s spironolactone hydrochloride tablets in the 25 mg, 50 mg and 100 mg strengths. The drug is a generic version of Pfizer’s Aldactone. Various versions of the drug had sales of $91 million in 2009, according to IMS Health.

 

 

August 26, 2010

The Food and Drug Administration has approved a single-pill combination of two drugs made by...

EAST HANOVER, N.J. The Food and Drug Administration has approved a single-pill combination of two drugs made by Novartis for treating high blood pressure, the Swiss drug maker said Friday.

 

The FDA approved Tekamlo (aliskiren and amlodipine besylate) tablets, which combine Tekturna (aliskiren) with amlodipine, a channel blocker available as a generic. The drug is approved for treating patients who are likely to need multiple drugs to lower their blood pressure or as a replacement for patients who can’t control it using one of the drugs alone.

August 26, 2010

Pfizer reported mixed results this week in a late-stage clinical trial combining two drugs in...

NEW YORK Pfizer reported mixed results this week in a late-stage clinical trial combining two drugs in patients with advanced non-small cell lung cancer.

The drug maker said the combination of Pfizer’s Sutent (sunitinib) and Tarceva (erlotinib), made by Genentech and OSI Pharmaceuticals, kept the disease from progressing, but did not improve patients’ overall survival, which was the trial’s primary goal. The company expects to present results at the European Society for Medical Oncology Congress in Milan in October.

August 19, 2010

An anti-inflammatory drug approved 60 years ago may help fight against a fungal infection of...

August 15, 2010

The Food and Drug Administration has approved a prefilled dual-chamber syringe made by Pfizer for...

NEW YORK The Food and Drug Administration has approved a prefilled dual-chamber syringe made by Pfizer for treating hemophilia, Pfizer said.

 

The FDA approved the syringe for administering the drug Xyntha (antihemophilic factor [recombinant]) for hemophilia A. The drug is used to prevent and control bleeding episodes in patients.

 

 

August 12, 2010

Prolatis earlier this week announced a voluntary nationwide recall of the company’s product sold under...

SALT LAKE CITY Prolatis earlier this week announced a voluntary nationwide recall of the company’s product sold under the brand name Prolatis’ after being informed by the Food and Drug Administration that lab analysis has found their male-enhancement products to contain sulfoaildenafil, an analogue of sildenafil, an FDA-approved drug used as treatment for male erectile dysfunction.

 

That makes Prolatis’ an unapproved drug, as opposed to a dietary supplement.

 

 

August 10, 2010

The drug market for unipolar depression will get smaller over the next decade due to...

August 4, 2010

Generex has appointed a Pfizer executive to help with its cancer and influenza vaccines program....

August 3, 2010

Pfizer had a big increase in sales and a modest increase in profits during second...

July 20, 2010

Pfizer is selling one of its New York properties to financial services firm TIAA-CREF, according...

July 19, 2010

Drug maker Pfizer is suspending some clinical studies of a biotech drug for treating pain...

July 18, 2010

A U.S. District Court has ruled in favor of two companies who alleged patent infringement...

July 13, 2010

Treatments for liver cancer could emerge from a new research partnership between the world’s largest...

June 30, 2010

Teva Pharmaceutical Industries has launched the first generic version of a drug used for treating...

June 28, 2010

An investigational treatment made by Daiichi Sankyo for hypertension significantly lowers blood pressure in patients...

June 28, 2010

The Food and Drug Administration has approved the first generic version of an extended-release antidepressant...

June 27, 2010

The Food and Drug Administrations has approved two new uses for what remains, thus far,...

June 23, 2010

Reports of worsening conditions among patients has led drug maker Pfizer to suspend a clinical...

June 22, 2010

Visine has developed a new eye-drop formula that relieves eye redness and irritation....

MORRIS PLAINS, N.J. Visine has developed a new eye-drop formula that relieves eye redness and irritation.

New Visine maximum redness relief formula uses a special Hydroblend formula to soothe irritation and provide up to ten hours of comfort, Visine said. In line with the product launch, Visine has developed a free app for iPhone and iPod Touch -- the Visine red eye remover application -- that eliminates red eye from consumers' photos in moments.

June 21, 2010

Pfizer has withdrawn one of its cancer drugs from the market at the request of...

June 16, 2010

Arthritis patients at risk of harmful gastrointestinal side effects due to use of a class...

June 14, 2010

The growth rate for employers’ medical costs is expected to fall somewhat next year, according...

June 10, 2010

Health insurer Blue Cross Blue Shield of Texas alleged that drug maker Pfizer marketed its...

June 6, 2010

Switch always has been the most significant driver of revenues within the non-prescription aisles, with...