FDA Approves Ella™ Tablets For Prescription Emergency Contraception

Links shared publicly online about this topic.

  • 949
    total visits

FDA Approves Ella™ Tablets For Prescription Emergency Contraception

medicalnewstoday.com

The U.S. Food and Drug Administration approved ella™ (ulipristal acetate) tablets for emergency contraception. The prescription-only product prevents pregnancy when taken orally within 120 h

View full resource at medicalnewstoday.com

Tags: Emergency, Drug, Sex and Intimacy, Pregnancy, FDA, Emergency Contraception

  • Share

Most Recently Shared on August 14, 2010 at 3:00 pm By:

mnt_drugapprov MNT Drug Approvals

FDA Approves Ella™ Tablets For Prescription Emergency Contraception http://mnt.to/3Hnh #regulatory

2 years ago...

Also Shared By:

medical_tweets medical_tweets

MNT Pharmacy News MNT Pharmacy News

MNT Sexual Health MNT Sexual Health

Dying mom's plea for investigational drug is heard. Friends and ABC Action news helps make it happen

abcactionnews.com — “We pride our selves in taking action for our viewers when and how we can. You may have seen a video on Facebook or YouTube about a local mom dying of breast cancer, pleading for a drug not yet approved by the FDA. Darlene Gant contacted me, Linda Hurtado, and together with a group of her very determined friends we got this mom the miracle chance she was praying for.View full resource at abcactionnews.com

  • View Related
  • Share

Most Recently Shared on April 23, 2012 at 1:59 am By:

medicallessons elaine schattner Physician, Doctor, Internist, Oncologist, and Hematologist

Woman, 46, w/ met breast cancer video-pleads FDA for drug (Pertuzumab), WashPo: http://t.co/S2pouEf6 -> ABC "action" - http://t.co/Ew9bdsIO

6 days ago...

FDA says focused on tracking drugs after approval | Reuters

reuters.com — “ATLANTA (Reuters) - The U.S. Food and Drug Administration said on Saturday it now spends as much effort and resources on surveilling a drug after it is approved as it does in the pre-approval process.TheView full resource at reuters.com

  • View Related
  • Share

Most Recently Shared on April 21, 2012 at 8:47 pm By:

HealthSociety Healthy Society Health News

FDA says focused on tracking drugs after approvalReutersBy Debra Sherman | ATLANTA (Reuters) - The US Food and D... http://t.co/JNtAA8e4

1 week ago...

Report: FDA strengthens monitoring of post-approval drug safety

fda.gov — “A strengthened and modernized postmarket drug safety program has resulted in a substantial improvement in the U.S. Food and Drug Administration’s oversight of drugs once they reach the American public, according to a new report released today by the agency’s Center for Drug Evaluation and Research (CDER). The report, “Advances in FDA’s Safety Program for Marketed Drugs,” describes new scientific tools and enhanced capabilities that give the same priority to postmarket drug safety monitoring as tView full resource at fda.gov

  • View Related
  • Share

Most Recently Shared on April 21, 2012 at 8:42 pm By:

HealthTrendster HealthTrendster Health Executive

Report: FDA strengthens monitoring of post-approval drug safety: A strengthened and… http://t.co/Nlax6RLR

1 week ago...

Consumer Group Warns Against Diabetes Drug | ThirdAge

thirdage.com — “  A consumer advocacy group is calling on government regulators to withdraw a diabetes drug from Novo Nordisk, saying the injectable medication raises the risk of thyroid cancer, pancreatitis and kidney failure. Public Citizen sent a petition to the Food and Drug Administration saying the risks of Victoza far outweigh its benefits as a diabetes drug, a crowded field that includes nearly a dozen similar medications. Citing internal agency documents, the group notes that FDA approved the drugView full resource at thirdage.com

  • View Related
  • Share

Most Recently Shared on April 20, 2012 at 12:03 am By:

thirdagetimes ThirdAge.com Health Site

Consumer Group Warns Against Diabetes Drug http://t.co/LS7h3N86

1 week ago...

Wrist worn multi-function vitals monitor by Sotera Wireless receives FDA clearance

imedicalapps.com — “Sotera Wireless receives FDA 510k approval for its ViSi Mobile body area network technology.View full resource at imedicalapps.com

  • View Related
  • Share

Most Recently Shared on April 17, 2012 at 1:29 pm By:

iMedicalApps iMedicalApps.com

Multi-function mobile vitals monitor by Sotera Wireless receives FDA clearance http://t.co/S5T387jI

2 weeks ago...

Agent Orange 2.0? Why Won’t The EPA Ban Toxic 2,4-D?

organicauthority.com — “The NRDC (National Resources Defense Council) did not have a good week. After news that the FDA dismissed a federal court ruling that the agency needed to enforce viable options for dealing with antibiotic resistant pathogens resulting from the overuse of antibiotics in livestock feed, word came that the EPA denied the organization's petition to ban the chemical 2,4-D. After news that the FDA dismissed a federal court ruling that the agency needed to enforce viable options for dealing with antibView full resource at organicauthority.com

  • View Related
  • Share

Most Recently Shared on April 16, 2012 at 7:38 pm By:

OrganicAuthorit Laura Klein Organic Advocate

Agent Orange 2.0? Why Won’t The EPA Ban Toxic 2,4-D? http://t.co/wCYxhDjb

2 weeks ago...

Device may ease back pain when all else fails | Health - Home

local10.com — “An FDA-approved implantable device may bring relief to people with incurable back pain.View full resource at local10.com

  • View Related
  • Share

Most Recently Shared on April 16, 2012 at 3:05 pm By:

BOTOX® Cosmetic (onabotulinumtoxinA) Celebrates 10-Year Anniversary of U.S. Food and Drug Administration Approval | BioPortfolio.com

bioportfolio.com — “From BioPortfolio: Allergan, Inc. (NYSE: AGN) announced today that April 15, 2012 will mark the 10-year anniversary of the U.S. Food and Drug Administrationâ??s (FDA) approv...View full resource at bioportfolio.com

  • View Related
  • Share

Most Recently Shared on April 13, 2012 at 1:46 pm By:

Dermatology_bio BioPF Dermatology Dermatology and Health News Feed

BioPortfolio News BOTOXÂ Cosmetic onabotulinumtoxinA Celebrates 10Year Anniversary of U.S. Foo... http://t.co/ogZ38usV BioPortfolio News

2 weeks ago...

Americans stuck on Botox for 10 years now – USATODAY.com

usatoday.com — “The toxin's popularity has skyrocketed, along with its medical uses, since FDA approval a decade ago this week.View full resource at usatoday.com

  • View Related
  • Share

Most Recently Shared on April 12, 2012 at 11:56 am By:

Is BPA the FDA’s Latest Gift to the Chemical Industry? | Organic Connections

organicconnectmag.com — “The FDA disappointed health advocates once again by allowing Bisphenol A or BPA, a known endocrine disruptor, to remain approved as a chemical additive in food containers such as plastic bottles and metal cans.View full resource at organicconnectmag.com

  • View Related
  • Share

Most Recently Shared on April 11, 2012 at 1:50 pm By:

organicconnect Organic Connections Health Magazine

Is #BPA the FDA’s Latest Gift to the Chemical Industry? | Organic Connections http://t.co/SWcE7Dog

3 weeks ago...

FDA extends review of Qnexa diet pill for three more months – USATODAY.com

usatoday.com — “The decision on whether to approve the new diet drug won't be until about July 17, instead of April 17.View full resource at usatoday.com

  • View Related
  • Share

Most Recently Shared on April 9, 2012 at 11:11 pm By:

USATODAYdiet Nanci Hellmich

FDA will spend three more months reviewing Qnexa diet pill http://t.co/fsn0h53G

3 weeks ago...

FDA Approves Alzheimer's Test Developed by Eli Lilly - WSJ.com

online.wsj.com — “The FDA approved an Eli Lilly test that can help detect Alzheimer's—a potential boon to treatment and developing drugs against the disease.View full resource at online.wsj.com

  • View Related
  • Share

Most Recently Shared on April 8, 2012 at 11:34 pm By:

Lilly says FDA approves brain imaging agent - Yahoo! News

news.yahoo.com — “From Yahoo! News: Eli Lilly and Co. said late Friday that the Food and Drug Administration approved Amyvid, a diagnostic imaging agent that is intended to help diagnose Alzheimer's disease.View full resource at news.yahoo.com

  • View Related
  • Share

Most Recently Shared on April 7, 2012 at 11:39 pm By:

Diagnostic_Test Diagnostic_Test OW Health

Lilly says FDA approves brain imaging agent: Eli Lilly and Co. said late Friday that the Food and Drug Administr... http://t.co/KiJpJNHt

3 weeks 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

3 weeks ago...

Pharmacy OneSource

rph.com — “The combined company of Pharmacy OneSource and Healthprolink enables swift and safe healthcare through innovative, web-based software solutions.View full resource at rph.com

  • View Related
  • Share

Most Recently Shared on April 5, 2012 at 5:14 pm By:

PharmOneSource Pharmacy OneSource

What did the FDA approve this week? Read to find out: http://t.co/FlA0waFm

3 weeks ago...

Advertisement