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Recent News and Articles on the Keywords: fda + unapproved + drugs  Related to the article below (Last Update: 12/1/2008)

 News results: Standard Version | Text Version | Image Version Results 1 - 10 of about 1,212 for fda unapproved drugs. (0.74 seconds) 
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Keep unapproved drugs out of patients? hands
AAP News (subscription) - 16 minutes ago
Unapproved Drugs: Drugs Marketed in the United States That Do Not Have Required FDA Approval is a Web site that provides tailored information to health care ...

ABC News
Health Buzz: Medicaid Covering Unapproved Drugs and Other Health News
U.S. News & World Report, DC - Nov 24, 2008
The Food and Drug Administration says that it is trying to squeeze unapproved drugs from the market, but certain federal laws allow Medicaid to continue to ...
Medicaid Paying for Unapproved Drugs Newsinferno.com
US Government Paying For Unapproved Drugs eFluxMedia
Study: Medicaid paid $198 million for unapproved drugs FierceHealthcare
InjuryBoard.com - dBTechno
all 650 news articles »
FDA Struggling To Weed Out Unapproved Drugs
Pharmaceutical Online (press release), PA - Nov 26, 2008
The FDA estimates that unapproved drugs account for 2 percent of all prescriptions filled by US pharmacies, about 72 million prescriptions a year. ...
Panel seeks warning on facial filler risks
El Paso Times, TX -
But a recent FDA hearing raised questions about unapproved uses, untrained technicians giving injections, and a lack of data on long-term safety. ...
Healthcare Education Campaign Will Track Drug Seizures Following ...
PR Web (press release), WA - Nov 28, 2008
eHealthInfoline.com will start tracking drug seizures following the recent FDA seizure of $24 Million in unapproved new drugs from a St. Louis-based ...
FDA Warns Bayer about Marketing Unapproved Drugs
Pharmaceutical Technology Magazine, NJ - Nov 6, 2008
FDA says the products are unapproved new drugs that require approved new drug applications to be legally marketed. The drugs? labels list uses that the ...

USA Today
? Just how safe is 'off-label' use of drugs?
The Oregonian - OregonLive.com, OR - Nov 26, 2008
The common, unsuccessful use of one drug is worrying enough. But doctors say there are dozens more drugs being used for unapproved reasons with inadequate ...
Off-label drug testing needed, study says United Press International
all 15 news articles »
Palm Beach drug injury lawyer, Susan Ramsey, says Medicaid has ...
Justice News Flash, FL - Nov 26, 2008
West Palm Beach drug injury lawyer, Susan Ramsey, injury attorney says Medicaid allows unsafe drugs. FDA unapproved drugs allows injuries and deaths. ...

New York Times
J&J helped plan child research institute -report
Reuters - Nov 24, 2008
Once approved, doctors are free to use a drug as they like, but companies cannot promote drugs for unapproved uses. According to documents submitted to the ...
Evidence in Risperdal Case Puts J&J on the Spot Wall Street Journal
Harvard?s Renowned Psychiatrist under Investigation for Drug Earnings eFluxMedia
J&J Backed Child Psychiatry Institute to Support Risperdal Sales Wall Street Journal Blogs
Philadelphia Inquirer
all 38 news articles »  JNJ
Study Calls for Greater Scrutiny of 'Off-Label' Drug Use
U.S. News & World Report, DC - Nov 24, 2008
Despite the scope of the practice, there's often little evidence that using a drug for an unapproved purpose is always beneficial or safe, a new study found ...
Source: Google News


 

Recent News and Articles on the Keywords: unapproved + drugs + fda  Related to the article below (Last Update: 8/7/2008)

The FDA's Black Box
Forbes, NY - 48 minutes ago
As a matter of law, the FDA must keep communications about unapproved drugs confidential. That silence reflects larger ways in which the agency is having ...SGP - OTC:SHRGY

The Money Times
FDA seizes unapproved drugs from St. Louis company
CNNMoney.com - Jul 30, 2008
NEW YORK (Associated Press) - Government agencies have seized more than $24 million worth of unapproved new drugs from St. Louis-based KV Pharmaceutical Co. ...
Agents seize $24M worth of unapproved drugs from KV Pharmaceutical Bizjournals.com
A real drug problem Las Vegas Sun
US seizes unapproved medicines at KV Pharmaceutical St. Louis Post-Dispatch
St. Louis Post-Dispatch
all 30 news articles »  KV.A
Federal Agents Seize More Than $24 Million In Unapproved New Drugs
Medical News Today (press release), UK - Aug 1, 2008
"Consumers need to be confident that the drugs and medical products they use are safe and effective, and the FDA will take the necessary measures to ensure ...
Expectorant seizure easy to swallow for KV In-PharmaTechnologist.com
Lannett Company Receives FDA Approvals for Doxycycline Tablets, 75 ... Business Wire (press release)
Lannett says FDA OKs Doxycycline Tablets, 75 mg and 150 mg - quick ... RTT News
SunHerald.com
all 25 news articles »  KV.A - LCI - AMS:WKL
Toxic Drugs, Toxic System: Sociologist Predicts Drug Disasters
Science Daily (press release) - Aug 4, 2008
5, 2008) ? Americans are likely to be exposed to unacceptable side effects of FDA-approved drugs such as Vioxx in the future because of fatal flaws in the ...
Federal Agents Seize Over $24 Million in Unapproved Drugs
Newsinferno.com, NY - Jul 31, 2008
US Food and Drug Administration (FDA) and US Marshals Service representatives just seized $24.2 million worth of unapproved drugs from KV Pharmaceutical ...KV.A

PhysOrg.com
FDA Failing to Monitor Unapproved Uses of Drugs
Newsinferno.com, NY - Jul 28, 2008
Also, under guidance proposed by the FDA this year, drug companies could distribute to doctors scientific articles that suggest new and unapproved uses for ...
FDA Poorly Equipped To Enforce Off-Label Prescription Drug ... Kaiser network.org
Marketing of Off-Label Drug Use Called into Question findingDulcinea
FDA?s Slow Handling of Problematic Drug Use eFluxMedia
Pharmalot - The Benton Crier
all 225 news articles »
US Congress slams FDA for off-label promotion control failures
Pharma Times (subscription), UK - Aug 4, 2008
Sheer volume prevents the FDA from reviewing all the promotional materials which are submitted to it by drug companies, so it prioritises its reviews in ...

The Associated Press
FDA faulted over unapproved uses of medications
The Associated Press - Jul 27, 2008
Also, under guidance proposed by the FDA this year, drug companies could distribute to doctors scientific articles that suggest new and unapproved uses for ...
$24 million in unapproved drugs seized from local pharmaceutical ...
St. Louis American, MO - Jul 29, 2008
Agents said the drugs were made after the FDA told the company to stop production. The drugs are used to treat coughs, colds and gastro-intestinal ...
Feds seize unapproved medication from St. Louis drug company KWMU
all 2 news articles »

BBC News
Generic drug makers? concern over Ranbaxy-USFDA stand-off
Hindu Business Line, India - Jul 17, 2008
... mixing of approved ingredients with unapproved ones and having reduced quantity of the pharmaceutical ingredient in a drug approved by the FDA. ...
Ranbaxy refutes DoJ's adulteration charges Economic Times
Ranbaxy Has Biggest Decline Since 2001 on US Probe (Update2) Bloomberg
Drug firm faces 'deception' claim BBC News
Times Online - Press Trust of India
all 412 news articles »  OTC:RBXLY - PRXL - PINK:DSKYF
Source: Google News

Dietary supplement or drug? The case of Cholestin -
RJ Havel - American Journal of Clinical Nutrition, 1999 - Am Soc Nutrition
... FDA determines Cholestin to be an unapproved drug. ... Elchisak MA, ed. Cholestin determined
to be unapproved drug by FDA 05/20/98. Drugs in the news: 1998 index. ...

Illegal use of beta-adrenergic agonists in the United States -
GA Mitchell, G Dunnavan - Journal of Animal Science, 1998 - Am Soc Animal Sci
... pounds of products containing unapproved drugs, valued at ... premix containing these
illegal and harmful animal drugs. ... Attorneys Office, US Customs, FDA, and USDA ...

DrugBank: a comprehensive resource for in silico drug discovery and exploration -
DS Wishart, C Knox, AC Guo, S Shrivastava, M … - Nucleic Acids Research - Oxford Univ Press
... small molecule drugs (>700 entries), (ii) FDA-approved biotech (protein ... 60 entries)
and (iv) experimental drugs, including unapproved drugs, de-listed ...

-
JO'Reilly, A Dalal - Annals Health L., 2003 - HeinOnline
Prescriber and Marketer Liability for Unapproved Uses of FDA-Approved Drugs James
O'Reilly' and Amy Dalal2 I. INTRODUCTION The year 2003 marks four decades ...

Internet Purchase of Prescription Drugs: Buyer Beware -
JE Henney, JE Shuren, SL Nightingale, TJ McGinnis - Annals of Internal Medicine, 1999 - annals.highwire.org
... an appropriate, Food and Drug Administration (FDA)-approved drug. ... medications, dangerous
drug interactions, contaminated drugs, or unapproved drugs that may ...

Imported Drugs Raise Safety Concerns: With an Unapproved Drug, You Can't Sure That It Has Been … -
M Meadows - FDA Consumer, 2002 - questia.com
... Although importing unapproved prescription drugs is illegal, the FDA's guidance
on importing prescription drugs for personal use recognizes that there may be ...

Why do american drug companies spend more than$ 12 billion a year pushing drugs? Is it education or … -
SM Wolfe - Journal of General Internal Medicine, 1996 - Springer
... it is currently illegal for drug companies to promote unapproved uses, legislation
introduced in the US Congress as part of the package of FDA-rollback pro ...

Benefit vs. Risk: How FDA Approves New Drugs.
D Farley - FDA Consumer, 1987 - questia.com
... before. Promising is the key word in this broadened use of unapproved drugs.
FDA can't allow drugs to be used haphazardly. "It's ...

[CITATION] A New Era of Unapproved Drugs: The Case of Abigail Alliance v Von Eschenbach -
PD Jacobson, WE Parmet - JAMA: The Journal of the American Medical Association, 2007 - JAMA
... should reject a constitutional right to unapproved drugs and give more weight to
the important public health interests served by the FDA's regulatory process. ...

Inflammatory Mass Lesions Associated with Intrathecal Drug Infusion Catheters: Report and … -
RJ Coffey, K Burchiel - Neurosurgery, 2002 - neurosurgery-online.com
... bupivacaine, and clonidine are not approved by the FDA for intrathecal ... a cascading
cellular immune stimulus, higher drug dosages and/or unapproved drugs, and a ...

Source: Google Scholar
 
 

FDA tells 3 companies to stop making unapproved drugs

U.S. authorities said on Thursday they told three companies to stop mass-producing and distributing unapproved medicines to treat asthma, bronchitis and other breathing disorders.

The Food and Drug Administration said the companies sold thousands of doses of inhaled drugs nationwide. The companies argued they were working under a practice known as "compounding" in which pharmacists customize formulations for specific patients, the FDA said.

The FDA allows compounding if a doctor prescribes something that meets a medical need and is unavailable in an approved product. A pharmacist, for example, could crush a tablet and mix it into a liquid for someone with trouble swallowing pills, or provide a version without a preservative that could cause an allergic reaction.

The three companies - Rotech Healthcare Inc, CCS Medical and Reliant Pharmacy Services - produced large quantities of unapproved drugs that did not provide benefits over approved medicines, the FDA said.

Joe Grillo, a spokesman for Reliant's parent Lincare Inc., said the company had no comment. Officials at Rotech and CCS Medical did not immediately return calls seeking comment.

The FDA said the products were inhaled drugs for treating asthma, emphysema, bronchitis and cystic fibrosis. Each of the conditions has FDA-approved treatments.

The medicines were distributed through mail order, Web sites and companies that sold devices used to inhale the medicines, said Steve Silverman, acting assistant director of compliance in the FDA's Center for Drug Evaluation and Research.

Officials urged patients to talk with their doctors and pharmacists to make sure they did not unknowingly receive some of the unapproved products.

"Compounded inhalation drugs are not reviewed by the FDA for safety and effectiveness, often are not produced according to good drug manufacturing practice, and typically are not sterile. This may expose patients to unnecessary risk," Dr. Steven Galson, director of the FDA's Center for Drug Evaluation and Research, said in a statement.

 
 
 
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