U.S. Food and Drug Administration

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U.S. Food and Drug Administration | Facebook

facebook.com — “Welcome to the official Facebook Page about U.S. Food and Drug Administration. Join Facebook to start connecting with U.S. Food and Drug Administration.View full resource at facebook.com

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Most Recently Shared on September 29, 2010 at 8:53 pm By:

jonmrich Jonathan Richman Health Executive

Good grief. Are any pharma employees going to be "Fans" of the FDA Facebook page? Sounds odd: http://www.facebook.com/FDA #hcsm

1 year ago...

U.S. Food and Drug Administration | Facebook

facebook.com — “Welcome to the official Facebook Page about U.S. Food and Drug Administration. Join Facebook to start connecting with U.S. Food and Drug Administration.View full resource at facebook.com

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Most Recently Shared on October 7, 2010 at 7:48 pm By:

eyeonfda eyeonfda Pharma and Health Lawyer

FDA's Favorite FB pages? White House, CDC, AIDS.gov and Healthcare.gov. http://ow.ly/2QeBN

1 year ago...

U.S. Food and Drug Administration | Facebook

facebook.com — “Welcome to the official Facebook Page about U.S. Food and Drug Administration. Join Facebook to start connecting with U.S. Food and Drug Administration.View full resource at facebook.com

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Most Recently Shared on November 17, 2010 at 1:02 am By:

Healthcare3dot0 Healthcare_3.0 Support

RT @iDailyScoop: #FDA on Fb http://on.fb.me/aagj05 Comment Policy" tab is glimpse of much needed pharma guidance policy #hcsmeu #hcsm

1 year ago...

HHS Opens U.S. Food and Drug Administration Offices in India

hhs.gov — “HHS Secretary Mike Leavitt and Commissioner of the HHS Food and Drug Administration (FDA) Andrew C. von Eschenbach, M.D., today marked the opening of the HHS/FDA offices in New Delhi, and Mumbai, India.View full resource at hhs.gov

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Most Recently Shared on January 15, 2009 at 4:15 pm By:

U.S. Food And Drug Administration Selects AB SCIEX To Provide Mass Spectrometry Systems For Food Contaminant Testing

medicalnewstoday.com — “AB SCIEX, a global leader in life science analytical technologies, announced that the U.S. Food and Drug Administration has purchased eight of the company's AB SCIEX QTRAP® 5500 Systems for anView full resource at medicalnewstoday.com

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Most Recently Shared on October 22, 2010 at 3:07 pm By:

mnt_medicaldev MNT Medical Devices Health News

U.S. Food And Drug Administration Selects AB SCIEX To Provide Mass Spectrometry Systems For Food Contaminant Testing http://mnt.to/3LBM

1 year ago...

Incyte Submits New Drug Application for Ruxolitinib in Myelofibrosis to the US Food and Drug Administration

drugs.com — “Ruxolitinib is a new drug in development for the treatment of myelofibrosis. Ruxolitinib information includes news, clinical trial results and side effects.View full resource at drugs.com

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Most Recently Shared on June 10, 2011 at 2:02 am By:

Drugs_Devices Drugs and Devices OW OW Health

Incyte Submits New Drug Application for Ruxolitinib in Myelofibrosis to the US Food and Drug Administratio... http://bit.ly/kCHd2A #drug

8 months ago...

U.S. Food And Drug Administration Keeps Rosiglitazone (Avandia) On The Market With Restrictions

medicalnewstoday.com — “The U.S. Food and Drug Administration (FDA) has announced that it will significantly restrict the use of the diabetes drug rosiglitazone (brand name, Avandia) to patients with Type 2 diabetes whoView full resource at medicalnewstoday.com

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Most Recently Shared on September 25, 2010 at 12:05 am By:

mnt_diabetes MNT Diabetes News Health News

U.S. Food And Drug Administration Keeps Rosiglitazone (Avandia) On The Market With Restrictions http://mnt.to/3Kjr #diabetes

1 year ago...

U.S. Food And Drug Administration Approves ABILIFY® (aripiprazole) For The Treatment Of Irritability Associated With Autistic Disorder In Patients

medicalnewstoday.com — “(BUSINESS WIRE)--Bristol-Myers Squibb Company (NYSE: BMY) and Otsuka Pharmaceutical Co., Ltd. announced that the U.S. Food and Drug Administration (FDA) has approved the supplemental New Drug ApplView full resource at medicalnewstoday.com

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Most Recently Shared on November 28, 2009 at 11:28 am By:

mnt_clinical MNT Clinical Trials Health News

U.S. Food And Drug Administration Approves ABILIFY® (aripiprazole) For The Treatment Of Irritability Associated.. http://bit.ly/51H21G

2 years ago...

U.S. Food And Drug Administration (FDA) Clears Novel ImageSenseTM Technology For Use With Colposcopy

medicalnewstoday.com — “STI Medical Systems, an industry leader in medical imaging systems and machine vision software, announced that the U.S. Food and Drug Administration (FDA) has given clearance to the Company's precView full resource at medicalnewstoday.com

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Most Recently Shared on January 9, 2011 at 11:10 am By:

Drugs_Devices Drugs and Devices OW OW Health

U.S. Food And Drug Administration (FDA) Clears Novel ImageSenseTM Technology For Use With Colposcopy:... http://mnt.to/f/3PMp #MedDevice

1 year ago...

ZOLL Propaq M Monitor Granted 510(k) Clearance By U.S. Food And Drug Administration

medicalnewstoday.com — “ZOLL Medical Corporation (NasdaqGS: ZOLL), a manufacturer of medical devices and related software solutions, announced that it has received 510(k) clearance from the U.S. Food and Drug AdministratView full resource at medicalnewstoday.com

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Most Recently Shared on September 23, 2010 at 1:34 pm By:

Drugs_Devices Drugs and Devices OW OW Health

ZOLL Propaq M Monitor Granted 510(k) Clearance By U.S. Food And Drug Administration: ZOLL Medical Corpor... http://mnt.to/f/3Kcm #MedDevice

1 year ago...

U.S. Food and Drug Administration Approves Crestor for Use in Pediatric Patients With Heterozygous Familial Hypercholesterolemia

drugs.com — “Crestor (rosuvastatin calcium) is used to treat pediatric patients with heterozygous familial hypercholesterolemia. Includes Crestor side effects, interactions and indications.View full resource at drugs.com

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Most Recently Shared on October 16, 2009 at 10:03 pm By:

drugscom Drugs.com Health Site

FDA Approves Crestor for Use in Pediatric Patients With Heterozygous Familial Hypercholesterolemia - http://bit.ly/DrHi0

2 years ago...

Auxilium Announces U.S. Food and Drug Administration Approval for Xiaflex for the Treatment of Dupuytren's Contracture

drugs.com — “Xiaflex (collagenase clostridium histolyticum) is used to treat Dupuytren's contracture. Includes Xiaflex side effects, interactions and indications.View full resource at drugs.com

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Most Recently Shared on February 3, 2010 at 10:07 pm By:

drugscom Drugs.com Health Site

Auxilium Announces FDA Approval for Xiaflex for the Treatment of Dupuytren's Contracture - http://bit.ly/cV10Uc

2 years ago...

Depomed Announces US Food and Drug Administration Approval of Gralise (gabapentin) Once-Daily Tablets for Treatment of Post-Herpetic Neuralgia

drugs.com — “Gralise (gabapentin) is used to treat post-herpetic neuralgia. Includes Gralise side effects, interactions and indications.View full resource at drugs.com

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Most Recently Shared on February 1, 2011 at 11:10 pm By:

Drugs_Devices Drugs and Devices OW OW Health

Depomed Announces US Food and Drug Administration Approval of Gralise (gabapentin) Once-Daily Tablets for ... http://bit.ly/eeb147 #drug

1 year ago...

Depomed Announces US Food and Drug Administration Approval of Gralise (gabapentin) Once-Daily Tablets for Treatment of Post-Herpetic Neuralgia

drugs.com — “Gralise (gabapentin) is used to treat post-herpetic neuralgia. Includes Gralise side effects, interactions and indications.View full resource at drugs.com

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Most Recently Shared on February 3, 2011 at 12:16 am By:

drugscom Drugs.com Health Site

Depomed Announces FDA Approval of Gralise (gabapentin) for Treatment of Post-Herpetic Neuralgia - http://bit.ly/hLaEa7

1 year ago...

U.S. Food And Drug Administration Keeps Rosiglitazone (Avandia) On The Market With Restrictions - QualityPoint Technologies

qualitypointtech.net — “The U.S. Food and Drug Administration (FDA) has announced that it will significantly restrict the use of the diabetes drug rosiglitazone (brand name, Avandia) to patients with Type 2 diabetes who cannot control their diabetes on other medications. Their decision is in response to data that suggest an increased risk of cardiovascular events, such as heart attack and stroke, in patients who were treated with rosiglitazone...View full resource at qualitypointtech.net

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Most Recently Shared on September 25, 2010 at 9:00 am By:

MedicalFeed MedicalFeed Health News Feed

U.S. Food And Drug Administration Keeps Rosiglitazone (Avandia) On The Market With Restrictions: The U.S. Food and... http://bit.ly/bgbNfQ

1 year ago...

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