FDA panel reviews telmisartan

Links shared publicly online about this topic.

  • 1,861
    total visits

FDA panel reviews telmisartan

theheart.org

UPDATED // The panel grappled with noninferiority margins and other statistical issues during the daylong hearing, and while it wouldn't give a wide indication for use in all high-risk cardiovascular patients, it felt that telmisartan is a good option for patients intolerant to the ACE inhibitor ramipril.

View full resource at theheart.org

Tags: Post Heart Attack Medication, Heart Failure Medication, High Blood Pressure Medication, FDA, Micardis, Delix, Tritace, Altace

  • Share

Most Recently Shared on July 29, 2009 at 9:39 pm By:

theheartorg Shelley Wood

heartwire: No to expanded indication for telmisartan, except in ramipril-intolerant patients, says FDA.. http://bit.ly/HGHJa

3 years ago...

Weight loss pill Qnexa wins panel vote and awaits approval

news-medical.net — “The drug was rejected in a 10-6 vote the first time it came before a Food and Drug Administration (FDA) advisory panel, in 2010, due to safety concerns. However when the medication returned for another review in February, the advisory committee gave it near-unanimous approval (20-2). Because the FDA often follows the advisory panel's advice, Qnexa is likely to get FDA approval, probably by mid-April.View full resource at news-medical.net

  • View Related
  • Share

Most Recently Shared on April 5, 2012 at 11:08 pm By:

Diet_News News-Medical.Net Health News

Diet News: Weight loss pill Qnexa wins panel vote and awaits approval: The drug was rejected in a 10-6 vote the ... http://t.co/rGbONdEq

2 months ago...

A.M. Vitals: Roberts Leaves Wiggle Room on Health-Law Case - Health Blog - WSJ

blogs.wsj.com — “Also: An FDA advisory panel recommends more testing to make sure obesity drugs don't cause heart attacks, and another FDA panel will review data on metal-on-metal him implants in June.View full resource at blogs.wsj.com

  • View Related
  • Share

Most Recently Shared on March 30, 2012 at 7:08 pm By:

UPDATE 2-FDA seeks more advice on metal hip implants | Reuters

reuters.com — “* FDA responds to concerns about all-metal hip implants* Advisory panel review set for June 27-28* Review could lead to more rigorous standardsMarch 29 (Reuters) - The U.S. Food and Drug AdministrationrespondedView full resource at reuters.com

  • View Related
  • Share

Most Recently Shared on March 29, 2012 at 8:00 pm By:

carybyrd Cary Byrd - eDrugSearch.com Pharma and Health Advocate

UPDATE 2-FDA seeks more advice on metal hip implants | Reuters http://t.co/4QjFaNXz

2 months ago...

FDA Panel Urges Review of Stryker Stent - WSJ.com

online.wsj.com — “A federal advisory panel said there was insufficient evidence to support keeping Stryker's Wingspan stent on the market, raising the possibility that the Food and Drug Administration might withdraw its approval of the stroke-treatment product.View full resource at online.wsj.com

  • View Related
  • Share

Most Recently Shared on March 26, 2012 at 12:39 am By:

Medical News:FDA Panel Review May Ground Wingspan Stent - in Cardiovascular, Prevention from MedPage Today

medpagetoday.com — “Medical News:FDA Panel Review May Ground Wingspan Stent - in Cardiovascular, Prevention from MedPage TodayView full resource at medpagetoday.com

  • View Related
  • Share

Most Recently Shared on March 24, 2012 at 3:49 am By:

MedicalFeed MedicalFeed Health News Feed

FDA Panel Review May Ground Wingspan Stent: WASHINGTON (MedPage Today) -- An FDA advisory… http://t.co/6tXijhDV

2 months ago...

FDA Panel Review May Ground Wingspan Stent - QualityPoint Technologies

qualitypointtech.net — “WASHINGTON (MedPage Today) -- An FDA advisory committee has indicated that there is insufficient evidence to say that the Wingspan intracranial stent has a long-term benefit that outweighs the device's risks.View full resource at qualitypointtech.net

  • View Related
  • Share

Most Recently Shared on March 24, 2012 at 3:45 am By:

MedicalFeed MedicalFeed Health News Feed

FDA Panel Review May Ground Wingspan Stent: WASHINGTON (MedPage Today) -- An FDA advisory committee has indicated ... http://t.co/NhNnwJEn

2 months ago...

Medical News:FDA Panel Review May Ground Wingspan Stent - in Cardiovascular, Prevention from MedPage Today

medpagetoday.com — “Medical News:FDA Panel Review May Ground Wingspan Stent - in Cardiovascular, Prevention from MedPage TodayView full resource at medpagetoday.com

  • View Related
  • Share

Most Recently Shared on March 24, 2012 at 3:12 am By:

Panel to Review Merck, Glaxo Cancer Drugs - WSJ.com

online.wsj.com — “An FDA panel on Tuesday will review new cancer drugs by Merck and Glaxo.View full resource at online.wsj.com

  • View Related
  • Share

Most Recently Shared on March 16, 2012 at 4:27 pm By:

UCLA Professor Says Qnexa Has The "Highest Efficacy" for Weight Loss

emaxhealth.com — “After a second review of its effectiveness and safety profile, Qnexa, an anti-obesity drug by Vivus Inc, has gained an FDA panel's approval and may so...View full resource at emaxhealth.com

  • View Related
  • Share

Most Recently Shared on February 23, 2012 at 5:05 pm By:

healthycarolina Denise Reynolds RD Nutritionist and Dietitian

UCLA Professor on FDA Panel Says Qnexa Has The "Highest Efficacy" for Weight Loss http://t.co/tCgqYnQr

3 months ago...

UPDATE 2-US FDA staff focus on safety of Forest lung drug | Reuters

reuters.com — “* Drug worked to treat chronic lung disease-FDA staff* Uncertain signals about heart safety with drug* FDA advisory panel to review drug on ThursdayBy Anna YukhananovWASHINGTON, Feb 21 (Reuters) -View full resource at reuters.com

  • View Related
  • Share

Most Recently Shared on February 21, 2012 at 2:24 pm By:

FiercePharma FiercePharma Health Site

RT @JohnCFierce: FDA regulators like Forest COPD drug's efficacy, but raise questions on cardio risks for the class. http://t.co/qxyBK25k

3 months ago...

FDA notes concerns about Vivus diet pill safety ahead of panel - FierceBiotech

fiercebiotech.com — “U.S. regulators have cited concerns about the safety of Vivus’ ($VVUS) experimental diet pill Qnexa in review documents as the California drug developer pursues the first FDA approval of a Read more...View full resource at fiercebiotech.com

  • View Related
  • Share

Most Recently Shared on February 17, 2012 at 3:52 pm By:

FierceBiotech FierceBiotech Health News

FDA notes concerns about Vivus diet pill safety ahead of panel http://t.co/Z8Nc7jXR $VVUS

3 months ago...

UPDATE 1-Pfizer says its drug is best hope for Alzheimer's - Yahoo! Finance UK

uk.finance.yahoo.com — “Read 'UPDATE 1-Pfizer says its drug is best hope for Alzheimer's' on Yahoo! Finance UK. * Says prior trials suggest edge over Lilly Alzheimer's drug * Says Prevnar 13 pneumonia data expected by 2013 * Expects FDA panel to review arthritis drug (Adds quotes from research chief, details on ...View full resource at uk.finance.yahoo.com

  • View Related
  • Share

Most Recently Shared on February 14, 2012 at 7:37 pm By:

Alzheimer_OW OrganizedWisdom AD OW Health

UPDATE 1-Pfizer says its drug is best hope for Alzheimer's: * Says prior trials suggest edge over Lilly Alzheime... http://t.co/I53zjiUn

3 months ago...

Oops, She Did It Again! FDA Disinvites Another Advisor - Yahoo! News

news.yahoo.com — “From Yahoo! News: Today an FDA advisory panel will meet to review the safety of oral contraceptives that contain drospirenone. One person who will not be voting on the panel is Sidney Wolfe, the well known consumer advocate and pharma critic. Wolfe was originally listed as a panel member, but then, only 2 days before the [...]View full resource at news.yahoo.com

  • View Related
  • Share

Most Recently Shared on December 10, 2011 at 8:11 am By:

maggiemahar Maggie Mahar Doctor and PhD

Oops, She Did It Again! FDA Disinvites Another Advisor - Yahoo! News http://t.co/bCXrBgJs via @YahooNews

6 months ago...

Oops, She Did It Again! FDA Disinvites Another Advisor - Forbes

forbes.com — “Today an FDA advisory panel will meet to review the safety of oral contraceptives that contain drospirenone. One person who will not be voting on the panel is Sidney Wolfe, the well known consumer advocate and pharma critic. Wolfe was originally listed as a panel member, but then, only 2 days before the [...]View full resource at forbes.com

  • View Related
  • Share

Most Recently Shared on December 8, 2011 at 3:21 pm By:

sstrumello Scott Strumello Patient Expert

Oops, She Did It Again! FDA Disinvites Another Advisor - Forbes http://t.co/PbW7RsNq

6 months ago...

FDA Gives Favorable Review to SHARP Ahead of Vytorin Advisory Panel - Forbes

forbes.com — “In preparation for Wednesday's meeting of the FDA's Endocrinologic and Metabolic Drugs Advisory Committee, an FDA reviewer has generally endorsed the positive interpretation of the  SHARP (Study of Heart and Renal Protection) trial of Vytorin (ezetimibe and simvastatin) in chronic kidney disease (CKD). Based on the results of SHARP Merck is seeking [...]View full resource at forbes.com

  • View Related
  • Share

Most Recently Shared on October 30, 2011 at 9:01 pm By:

Drugs_Devices Drugs and Devices OW OW Health

FDA Gives Favorable Review to SHARP Ahead of Vytorin Advisory Panel: In preparation for Wednesday’s meetin... http://t.co/vYawcGFW #drug

7 months ago...

Advertisement