Iconocast Logo

Welcome To Iconocast

How to add a URL link from your web site to the Iconocast web sites

Virtual tour of Southern California



 

Recent News and Articles on the Keywords: fda + regulation + does  Related to the article below (Last Update: 8/5/2008)

Actavis Totowa Finally Does The Right Thing
US Recall News (press release), CO -
Back in May US Recall News uncovered an FDA report released in the summer of 2006 that outlines some of the FDA?s findings on the substandard quality ...

Ontario Now
House approves FDA regulation of tobacco
Bizjournals.com, NC - Jul 31, 2008
Reynolds American Inc., based in Winston-Salem, also opposes FDA regulation on tobacco. It has a smaller menthol market share than Lorillard, ...
With FDA Gaining Power Over Tobacco, They Can Protect Kids dBTechno
ANDREA HOPKINS: Big Tobacco?s Unholy Influence On Congress Is Waning TriCities.com
google news commentComment by M. Cass Wheeler Chief Executive Officer,American Heart Association
Stogie Guys Online Cigar Magazine - California Healthline
all 557 news articles »  NYT

Chatter Shmatter
Connecticut AG: Sunscreen Makers' Claims 'Misleading'
Environment News Service - Aug 4, 2008
"For far too long sunscreen manufacturers have exploited the FDA's abject failure to enact regulations that ensure truthful, accurate claims in sunscreen ...
Almost Half of Sunscreens 'Do Not Offer Protection' Holiday hypermarket
Many Sunscreens Do Not Protect Against Sun?s Harmful Rays dBTechno
Skin cancer alert Gulf Daily News
Telegraph.co.uk - Canada.com
all 254 news articles »

Pharmalot
FDA to weed out conflict of interest in advisory committees
Medical Marketing and Media, NY -
The FDA has tightened regulations on financial conflict of interest among committee members, and will increase public disclosure in several areas. ...
FDA Issues New Rules For Advisory Committees Pharmalot
all 132 news articles »
Single-Pill Combinations Diovan HCT and Exforge Approved in US as ...
MarketWatch - Aug 3, 2008
The FDA approval of Diovan HCT and Exforge for first-line use reinforces current US guideline recommendations to start appropriate patients on combination ...

Chatter Shmatter
Trials and Medications
RedOrbit, TX - Aug 4, 2008
The US Food and Drug Administration (FDA) demands a rigorous regimen of testing for any new product a pharmaceutical firm wants to bring to the marketplace. ...
US Congress slams FDA for off-label promotion control failures Pharma Times (subscription)
FDA Releases List of Genomic Biomarkers Predictive of Drug ... Medscape (subscription)
FDA Forces New Labeling for Procrit, Aranesp and Epogen Newsinferno.com
Reuters - Trading Markets (press release)
all 222 news articles »  NYT - AMGN - JNJ

Chatter Shmatter
Injected High Blood Pressure Drug Approved by FDA
HULIQ (press release), NC -
Cleviprex is different from other High Blood Pressure drugs in that it does not accumulate in the body. The metabolism of Cleviprex takes place in tissues ...
Medicines Receives FDA Approval To Market IV Blood Pressure Drug ... RTT News
The Medicines Company?s Cleviprex? Receives FDA Approval Business Wire (press release)
all 36 news articles »  MDCO
Lawmakers Crack Down on FDA?s Environmental Policy
FDA news (subscription), VA -
... its proposed regulation of mercury-related dental devices was excluded from NEPA and did not require an EA because the devices were ?of a type that does ...
Health: Organic Skin Care
CBS 3, PA -
But the USDA doesn't regulate cosmetics, the FDA does. And there is no FDA definition of the term organic. The FDA also doesn't define terms like "natural," ...
Eli Lilly spent nearly $2.9M lobbying in 2Q
MSN Money -
Generic drug companies already market cheaper versions of regular, chemical drugs, but the FDA does not have the authority to approve copies of biotech ...LLY
Source: Google News

The New HIPAA (Health Insurance Portability and Accountability Act of 1996) Medical Privacy Rule … -
J Kulynych, D Korn - Circulation, 2003 - Am Heart Assoc
... Moreover, both the Common Rule and FDA regulations require IRBs to make an explicit ...
critics state that the existing system of IRB oversight does not ensure ...

Direct-to-Consumer Marketing of Prescription Drugs Creating Consumer Demand -
MF Hollon - JAMA, 1999 - Am Med Assoc
... FDA regulation of prescription drug advertising. ... FDA public hearing: direct-to-consumer
promotion. ... and treatment of respiratory infections: does managed care ...

FDA Regulation of Stem-Cell-Based Therapies -
DG Halme, DA Kessler - New England Journal of Medicine, 2006 - content.nejm.org
... new drug application to the FDA before studies ... Get Slide, Table 1. Highlights of
Regulations Applicable to ... to address the following questions: Does the donor ...

'PROTECTING AMERICA'S HEALTH: The FDA, Business, and One Hundred Years of Regulation'. -
RJ White - Oncology Times, 2003 - oncology-times.com
... And it does appear that at almost every confrontation ... finally put into effect by
the FDA that formed ... In order to comply with these regulations, the commercial ...

The Need for Regulation of Dietary Supplements-Lessons From Ephedra -
PB Fontanarosa, D Rennie, CD DeAngelis - JAMA, 2003 - Am Med Assoc
... is right to be alarmed that the regulation Congress has in place does so little
to ... and Human Services Secretary Tommy Thompson and FDA Commissioner Mark ...

Americans'Views on the Use and Regulation of Dietary Supplements -
RJ Blendon, CM DesRoches, JM Benson, M Brodie, DE … - Archives of Internal Medicine, 2001 - Am Med Assoc
... Toward FDA Regulation of Supplements* Total (N = 1196) Frequency of Dietary Supplement
Use Regular (n = 235) Sometimes (n = 381) Never (n = 580) Does the ...

Toward a More General Theory of Regulation -
S Peltzman - The Journal of Law and Economics, 1976 - UChicago Press
... (1994) Wealth effects of food and drug administration (FDA) decisions. ... (1986)
Does regulation reduce electricity rates? A research note. ...

-
RR Munsey - Food & Drug LJ, 1995 - HeinOnline
... 360j(i). MEDICAL DEVICE REGULATION marketed device and does not raise ... a manufacturer
from commercially distributing a device until the FDA has entered ...

[BOOK] Hazardous to Our Health?: FDA Regulation of Health Care Products
R Higgs - 1995 - Independent Institute

Are Surrogate Markers Adequate to Assess Cardiovascular Disease Drugs? -
R Temple - JAMA, 1999 - Am Med Assoc
... or suggested in the proposed labeling." 11 This wording plainly does not suggest ...
value to be a basis for approval until a 1992 FDA regulation on "accelerated ...

Source: Google Scholar
 

What products does FDA regulate?

Consumers can play an important public health role by reporting to FDA any adverse reactions or other problems with products the agency regulates. FDA is responsible for ensuring that foods are safe, wholesome, and correctly labeled. It also oversees medicines, medical devices (from bandages to artificial hearts), blood products, vaccines, cosmetics, veterinary drugs, animal feed, and electronic products that emit radiation (such as microwave ovens and video monitors), ensuring that these products are safe and effective.

Why should I report?

The testing that helps to establish the safety of products, such as drugs and medical devices, is typically conducted on small groups before FDA approves the products for sale. Some problems can remain unknown, only to be discovered when a product is used by a large number of people.

Article continues below and (thank you)

 

When problems with FDA-regulated products occur, the agency wants to know about them and has several ways for the public to make reports. Timely reporting by consumers, health professionals, and FDA-regulated companies allows the agency to take prompt action. The agency evaluates each report to determine how serious the problem is, and, if necessary, may request additional information from the person who filed the report before taking action.

 

How do I report an emergency?

If the situation is an emergency that requires immediate action, such as a case of food-borne illness or a drug product that has been tampered with, call the agency's main emergency number, staffed 24 hours a day, 301-443-1240.

You also can report emergencies, as well as non-emergencies, to the FDA consumer complaint coordinator in your geographic area.

Situations that do not require immediate action--such as a non-emergency adverse reaction to a food product or an over-the-counter medical device that doesn't work as advertised--can be reported either to the appropriate consumer complaint coordinator or to the FDA office that handles the product.

 

How do I report non-emergencies about food?

To report problems, including adverse reactions, related to any food except meat and poultry, contact the district office consumer complaint coordinator for your geographic area.

If the problem involves meat or poultry, which are regulated by the U.S. Department of Agriculture, call the USDA hotline at 1-800-535-4555.

 

How do I report non-emergencies about medical products: medicines, medical devices, blood products, biologics, special nutritionals?

MedWatch -- The FDA Safety Information and Adverse Event Reporting Program allows healthcare professionals and consumers to voluntarily report serious problems that they suspect are associated with the drugs and medical devices they prescribe, dispense, or use. These problems include serious adverse reactions and events, product quality problems, and product use errors. Reporting can be done online, by phone, or by submitting the MedWatch 3500 form by mail or fax. Visit the MedWatch How To Report page for more details.

 

How do I report non-emergencies about vaccines?

Adverse reactions and other problems related to vaccines should be reported to the Vaccine Adverse Event Reporting System, which is maintained by FDA and the Centers for Disease Control and Prevention. For a copy of the vaccine reporting form, call 1-800-822-7967 or get a copy of the form from the FDA Website.

 

How do I report non-emergencies about blood transfusions and donations?

You can make initial notifications of transfusion-related fatalities and donation-related deaths to FDA's Center for Biologics Evaluation and Research.

 

How do I report non-emergencies about animal feed/food?

To report problems, including adverse reactions, related to any food for animals, contact the district office consumer complaint coordinator for your geographic area.

 

How do I report non-emergencies about veterinary products?

Report any problems with veterinary drugs and devices for animals to FDA's Center for Veterinary Medicine at 1-888-FDA-VETS (1-888-332-8387). You can also find the reporting form on the center's Website.

 

How do I report non-emergencies about cosmetics?

People can report a bad reaction to face paint, novelty makeup, or any other cosmetic product to:

  • Your nearest FDA district office. Their phone numbers are on FDA's Web site and in the Blue Pages of the phone book under United States Government/Health and Human Services.
  • FDA's Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System (CAERS) by phone at 301-436-2405 or by email at CAERS@cfsan.fda.gov.

 

How do I report non-emergencies about products sold online?

If you find a Website you think is illegally selling human drugs, animal drugs, medical devices, biological products, foods, dietary supplements, or cosmetics over the Web, you may report it to FDA using the form on this Website.

 

What should I include in my report?

  • Report what happened as soon as possible. Give names, addresses and phone numbers of persons affected. Include your name, address and phone number, as well as that of the doctor or hospital if emergency treatment was provided.
  • State the problem clearly. Describe the product as completely as possible, including any codes or identifying marks on the label or container. Give the name and address of the store where the product was purchased and the date of purchase.
  • You also should report the problem to the manufacturer or distributor shown on the label and to the store where you purchased the product.

 

What kinds of problems doesn’t FDA handle and where can I report them?

Reports and complaints about the following should be made to the agencies listed. Phone numbers can be found in your local phone directory:

  • Restaurant food and sanitation--Local or state health departments
  • Unsolicited products in the mail--U.S. Postal Service
  • Accidental poisonings--Poison control centers or hospitals
  • Pesticides or air and water pollution--U.S. Environmental Protection Agency
  • Hazardous household products (including toys, appliances, and chemicals)--Consumer Product Safety Commission, 1-800-638-2772
  • Alcoholic beverages--Department of Treasury's Bureau of Alcohol, Tobacco and Firearms
  • Drug abuse and controlled substances--Department of Justice's Drug Enforcement Administration
  • Hazardous chemicals in the workplace--Department of Labor's Occupational Safety and Health Administration
  • Warranties--Federal Trade Commission
  • Dispensing and sales practices of pharmacies--State board of pharmacy
  • Medical practice--State certification board

 

How can I get information about the products FDA regulates?

If you have a general question about an FDA-regulated product, call toll-free 1-888-INFO-FDA (1-888-463-6332). But please don't report problem products or adverse reactions to this number. Instead, contact FDA's consumer complaint coordinators.

 
 
 
Google
Web www.iconocast.com
 
 
Continue News With: News9 ; News9A


ADVERTISEMENT

Iconocast is about learning and teaching without borders; we offer eMarketing, Internet Advertising, Internet Marketing, Search Engine Optimization, Search Engine Marketing, Online Branding, and eMarketing News Services.

 

Iconocast Home Page

 © 2002-2006

Keywords:

Contact Iconocast