Blog Posts - Fda



FDASIA Health IT Report Issued; Comments Welcomed on Three-Agency Approach

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Simple Invention For Sealing Gunshot Wounds Gets FDA Approval

XStat Photograph by Ralph Smith The pocket-sized XStat, a hemorrhage-stopping invention we wrote about in February , yesterday received approval from the U.S. Food and Drug Administration as a first-of-its-kind medical dressing. This means that the U...
by Cnet Analysis on Apr 4, 2014

How a PepsiCo flavor partner fooled Wall Street and the press

        (Media Release) For years, the processed-food industry has searched in vain for a low-calorie sweetener that actually tastes good, let alone one that retains the flavor profile of the underlying product. In 2010, the food...
by Free PR Online on Mar 20, 2014

Safety advisory posted after four deaths from HeartMate II® LVAS Pocket System Controller

Medical device not being recalledAfter four deaths and five reports of loss of consciousness or other symptoms of hypo-perfusion, Thoratec Corporation initiated a voluntary worldwide medical device correction to update its labeling and training mate...
by Barbara's Beat on Mar 5, 2014

News about Federal Records issue #1

Despite subsidies, digital medical-records industry fights opposes FDA oversight – Columbus Dispatch – dispatch.com 03/02/2014 Despite subsidies, digital medical-records industry fights opposes FDA oversightColumbus DispatchWASHINGTON —...

HEALTH - Why Nutrition Label Makeover?

"Why U.S. nutrition labels will be getting a makeover" PBS Newshour 2/27/2014JUDY WOODRUFF (Newshour):  For the first time in two decades, the federal government is making significant changes to the nutrition labels on the food and drinks you bu...
by Mage Soapbox on Mar 1, 2014

Hepatitis - FDA Label update for Victrelis (boceprevir)

The Victrelis (boceprevir) label has been updated to include the following information under Section 5 Warnings and Precautions:5.4 Pancytopenia (Use with Ribavirin and Peginterferon Alfa) Pancytopenia is a medical condition in which there is a...
by HCV New Drug Research on Feb 12, 2014

Why A Business Has A Voluntary Recall Of A Product

Every day the Food and Drug Administration receives voluntary recalls from companies. Consumers have the option to sign up on their website to receive email alerts about product recalls. So, why would a company voluntarily recall a product? If no one...
by Business Diary Philippines on Feb 7, 2014

15 Accounts Super King Package Royale

posted by rom5stars | Networking - MLM Offered | P193320.00 | 0 post 31 Accounts Super King Package Royale Business Club (Guaranteed commission check of 43,020 pesos) Be an independent distributor of PROVEN EFFECTIVE AND SAFE PROD...

Finally FDA warns about using muscle growth products

The U.S. Food and Drug Administration is advising consumers to immediately stop using a product called Mass Destruction, marketed as a dietary supplement for muscle growth. The product is labeled to... [[ This is a content summary only. Visit my web...
by pharmacy training on Jan 23, 2014

FDA Drug Safety Concerns About Pradaxa And Serious Bleeding Side Effects Will Get Another Look By Means Of New 2014 Study

A Primary Focus Is Gastrointestinal And Intracranial Hemorrhages In Patients Using Pradaxa For Atrial Fibrillation (Posted by Tom Lamb at DrugInjuryWatch.com) Pradaxa, an anticoagulant drug from Boehringer Ingelheim, was approved by drug regulators i...
by Drug Injury Watch on Jan 15, 2014

FDA (Fools Demanding Authority) Has Finally Made A Stance About The Use Of Antibiotics In Healthy Animals

Our overwhelmed federal agency, issued a written statement which is essentially a voluntary policy to “limit” using antibiotics for sick animals only. Depending on the food industries honesty levels is akin to saying that our government w...
by Renovating Your Mind on Dec 22, 2013

Nuove Strade per myGenomix

Con grande piacere e con un pizzico di orgoglio vi annuncio che da oggi potrete leggere qualche mio articolo sulla nuova rivista online Strade. In questo magazine si parla soprattutto di politica e di economia (argomenti sui quali non sono certo un e...
by myGenomiX on Dec 4, 2013

Nuove Strade per myGenomix

Con grande piacere e con un pizzico di orgoglio vi annuncio che da oggi potrete leggere qualche mio articolo sulla nuova rivista online Strade. In questo magazine si parla soprattutto di politica e di economia (argomenti sui quali non sono certo un e...
by myGenomiX on Dec 4, 2013

FDA:No elevated risk of heart attack or death in patients on Avandia

The U.S. Food and Drug Administration today announced it is requiring the removal of certain restrictions on prescribing and use of the diabetes drug Avandia (rosiglitazone) to reflect new... [[ This is a content summary only. Visit my website fo...
by pharmacy training on Nov 29, 2013

La FDA dichiara guerra a 23andMe: a rischio il Facebook della genetica

“Vi preghiamo di comunicare al presente ufficio, entro quindici giorni lavorativi dal ricevimento di questo lettera, le specifiche azioni che avete intrapreso per rispondere alle questioni sollevate più sopra. Includete la documentazione relat...
by myGenomiX on Nov 26, 2013

La FDA dichiara guerra a 23andMe: a rischio il Facebook della genetica

“Vi preghiamo di comunicare al presente ufficio, entro quindici giorni lavorativi dal ricevimento di questo lettera, le specifiche azioni che avete intrapreso per rispondere alle questioni sollevate più sopra. Includete la documentazione relat...
by myGenomiX on Nov 26, 2013

Mobile Health Apps: Pass the Secret Sauce

We've Moved! Update your Reader Now. This feed has moved to: http://feeds.healthblawg.com/healthblawg Update your reader now with this changed subscription address to get your latest updates from us. http://feeds.healthblawg.com/healthblawg...

Hepatitis C - Changes to Incivek (telaprevir) product labeling

Changes to Incivek (telaprevir) product labelingSource FDA 10/29/2013 Changes to Incivek (telaprevir) product labeling FDA approved changes to the Incivek (telaprevir) product labeling to include results from trial C211 (OPTIMIZE) to support a twic...
by HCV New Drug Research on Oct 30, 2013

Study questions FDA's shorter drug approval times

Study questions FDA's shorter drug approval times By Toni ClarkeWASHINGTON | Tue Oct 29, 2013 12:54am EDT (Reuters) - New drugs that receive expedited review by the Food and Drug Administration are being tested on fewer patients, leavin...
by HCV New Drug Research on Oct 29, 2013


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