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y pled guilty to a single count of lying to the FDA about the adverse effects of Metabolife 356.
In 2005 the U.S. Food and Drug Administration ( FDA) accepted Cortex Pharmaceuticals' Investigation
In 2009, the FDA added minocycline to its Adverse Event Reportin
A recipient of a 483 should respond to the FDA, addressing each item, indicating agreement and
ily withdrawn from the market after a July 2005 FDA advisory warned of a high overdose potential wh
United States on August 13, 2010, following the FDA advisory committee's recommendation.
On September 8, 2010 the FDA Advisory Committee recommended approval for the
Also in 2009, an FDA advisory committee unanimously recommended Beva
FDA Advisory on star anise "teas"
was banned by the Food and Drug Administration ( FDA) after its carcinogenicity in rats was discover
and efficacy raised in the public comments, the FDA again determined that the vaccine is licensed f
The FDA alleges a relationship between prescriptions of
The FDA also is requiring manufacturers to update label
The FDA also made a policy that companies could not for
The authors of the FDA analysis note that "given the large number of c
The U.S. Food and Drug Administration ( FDA) and international health authorities have publ
lture (USDA), the Food and Drug Administration ( FDA) and the Environmental protection agency (EPA).
that the Janus data repository would enable the FDA and the pharmaceutical industry to both look re
by what they perceived as collusion between the FDA and food conglomerates, put pressure on the FDA
ation (JPMA), the Food and Drug Administration ( FDA), and the Pharmaceutical Research and Manufactu
ithKline is currently being investigated by the FDA and the US Congress regarding Avandia.
ast few decades moving between Monsanto and the FDA and USDA.
illapur facility facility was re-audited by the FDA and approved, following the filing of an ANDA b
the only contraceptive implant approved by the FDA and sold in the United States.
s" Revealed, Trudeau writes that workers at the FDA and FTC want to censor him and, figuratively, b
thods are recognized as official methods by the FDA and other agencies.
ablished in 1990, and is managed jointly by the FDA and the CDC.
as received Orphan Drug designation by both the FDA and the European Medicines Agency.
these years he worked with local organizations FDA and FLOT, acting in community theatre and high
ication to the US Food and Drug Administration ( FDA) and as a result of discussion with the FDA Jer
Following authorization by the FDA and USDA, Castleberry's Food Company restarted
The FDA and the manufacturer also warn that some patien
, outdoor laser use is jointly regulated by the FDA and the Federal Aviation Administration.
Competitiveness and Regulation: The FDA and the Future of America's Biomedical Industry
vestigational New Drug Application (IND) to the FDA and began Phase I, II, and III clinical trials
r 2, 2009, the US Food and Drug Administration ( FDA) and Sanofi-Aventis are warning healthcare prof
ults of the full analyses were disclosed to the FDA and reflected on the Vioxx warning label.
roved by the U.S. Food and Drug Administration ( FDA) and is a leading example of personalized medic
cers, packagers, handlers) to register with the FDA and pay an annual fee of $500 per facility.
the United States Food and Drug Administration ( FDA) announced that Elidel packaging would be requi
8, 2009, the U.S. Food and Drug Administration ( FDA) announced that Coartem was approved for the tr
The U.S. Food and Drug Administration ( FDA) announced on 2 June 2009 that the drug has bee
er 2007, the U.S. Food and Drug Administration ( FDA) announced that a warning about possible deafne
In September 2010 and appeal, the FDA announced that it would begin regulating e-ciga
On the same day as the FDA announcement, Novartis Pharmaceuticals Canada a
The FDA anticipates completing its review of this appli
On April 28, 2011, the FDA Antiviral Drugs Advisory Committee voted 18-0 t
Due to frequent controversies involving the FDA, appointments are not always prompt and the age
Adeza Biomedical (October 23, 2006) Receives FDA Approvable Letter For Gestiva
Ipodate sodium lacks FDA approval for this use.
atin, obtained US Food and Drug Administration ( FDA) approval in 1978 and went on to become a widel
Geigy gained FDA approval for the drug in December 1986.
Olsalazine gained Food and Drug Administration ( FDA) approval in 1990.
al for the new drug, and the drug received full FDA approval on August 6, 2007 for use in treatment
October 5, 2000, Pharmacia received FDA approval for Lunelle Monthly Contraceptive Inje
ery procedures, and the work of his team led to FDA approval for cardiac robotic techniques includi
vine collagen for wrinkles and scars helped get FDA approval and launched the highly profitable fie
In March 2011, Daliresp gained FDA approval in the US for reducing COPD exacerbati
Its FDA approval helped bring down the price of zidovud
It gained Food and Drug Administration ( FDA) approval in April 1998, and is supplied by Mer
Ultimately, MAPS seeks to achieve FDA approval for the use of MDMA as a prescription
Ligand gained Food and Drug Administration ( FDA) approval for alitretinoin in February 1999.
Floxuridine first gained FDA approval in December 1970 under the brand name
a (who had by then merged with Upjohn) received FDA approval for the use of epirubicin as a compone
vaccines against HPV, the first of which earned FDA approval in 2006.
ns of NRTIs was in practice prior to the second FDA approval and the triple drug combinations with
Mylan Laboratories Inc. has received FDA approval for its generic version of Imitrex tab
first quarter 2010, Genasense had not received FDA approval due to disappointing results in a mela
e III of the U.S. Food and Drug Administration ( FDA) approval process.
Amgen Puerto Rico received FDA approval for bulk manufacturing facilities for
Because of this trial Sorafenib obtained FDA approval for the treatment of advanced hepatoce
ial is required before it can be considered for FDA approval in the United States.
Upjohn filed for FDA approval of streptozotocin as a treatment for p
Requires FDA approval for the use of expressions such as "li
through the U.S. Food and Drug Administration ( FDA) approval process
mmon form of liver cancer, in October 2007, and FDA approval for this indication followed in Novemb
It received FDA approval in 1991.
in the U.S. due to toxicity and never received FDA approval.
is drug, under the trade name Lucentis, now has FDA approval.
ss experimental medications before they receive FDA approval.
Inc., and was brought to market in 2005, after FDA approval.
sfully complete clinical development and obtain FDA approval.
te a phase III trial (CONCERT study) aiming for FDA approval.
FDA approved tagatose as a food additive in October
In the U.S. the FDA approved its use in wines in 1988, with the max
FDA approved this drug on October 9th, 2008.
If the FDA approved a system like UltraShape or SonoSculpt
It is not FDA approved to be used in children.
On April 27, 2006, FDA approved labeling changes concerning all form o
The study by Taylor et al., based on which the FDA approved the medication demonstrated that isoso
It is supplied in FDA approved food grade.
breakthroughs and discoveries in medicine, the FDA approved lifesaving treatment for Pompe disease
It is an U.S. Food and Drug Administration ( FDA) approved human monoclonal antibody developed b
ment Yellow 42 is Food and Drug Administration ( FDA) approved for use in cosmetics and is used in s
Visualase is not FDA approved for use in any specific cancer treatme
On February 28, 2008, the FDA approved a controlled-release formulation of fl
sitagliptin ( FDA approved 2006, marketed by Merck & Co. as Januv
On April 15, 2008, the US FDA approved a combination of sumatriptan and napro
the brand name Fareston, toremifene citrate is FDA approved for use in advanced (metastatic) breas
It is the only FDA approved drug to treat primary biliary cirrhosi
The FDA approved it October 20, 2003, while the EMEA ap
of 1986, the U.S. Food and Drug Administration ( FDA) approved it.
In 1970 the U.S. Food and Drug Administration ( FDA) approved LAL for testing drugs, products and d
plant natural product beta-caryophyllene is an FDA approved food additive and ingested daily with
VLPs have already been used to develop FDA approved vaccines for Hepatitis B and human pap
The FDA approved the drug for antidepressant use in Feb
The US FDA approved it for treatment of hyperammonaemia on
In 2010 the US FDA approved the use of Lucentis injections for mac
Medications are not FDA approved for use in this age group.
Undecylenic acid is a natural fungicide and is FDA approved in over-the-counter medications for sk
The FDA approved Seroquel XR for the treatment of bipol
On February 22, 2005, the US FDA approved a sustained release form of doxazosin,
The U.S. Food and Drug Administration ( FDA) approved dextromethorphan for over-the-counter
The services are US FDA approved and tested in-house, and conform to th
tes (U.S.) with a Food and Drug Administration ( FDA) approved indication for the treatment of restl
FDA approved application number (note that “other”
On August 22, 2008, the FDA approved romiplostim as a long-term treatment f
panies globally, primarily using one of the two FDA approved technologies.
In 2001 the U.S. FDA approved a proprietary formula of a solution of
The Food and Drug Administration ( FDA) approved the sale of a generic version of Flon
2, 2008, the U.S. Food and Drug Administration ( FDA) approved Cimzia for use in the United States f
The first orphan-drug for Genzyme that FDA approved was Ceredase, a drug for treating Gauc
The U.S. Food and Drug Administration ( FDA) approved human clinical trials for the intra-v
The Food and Drug Administration ( FDA) approved its sale as an over-the-counter treat
the body) in select patients although it is not FDA approved for this use.
In March 2009, the FDA approved the use of Symbicort pMDI to treat chr
The Food and Drug Administration ( FDA) approved indinavir March 13, 1996, making it t
All ingredients are USDA and FDA approved and the process has been licensed by t
ay 2003, the U.S. Food and Drug Administration ( FDA) approved Ibandronate as a daily treatment for
24, 2008, the US Food and Drug Administration ( FDA) approved difluprednate for the treatment of po
It is FDA approved for treating chronic lymphocytic leuke
used in a host of Food and Drug Administration ( FDA) approved therapeutic devices, owing to its bio
It is not FDA approved for human use as an antiarrhythmic age
Ertapenem ( FDA approved - for multiple indications)
lled BVA-100, Blood Volume Analysis is the only FDA approved instrument that provides a measure of
It gained FDA Approved in July 1969.
US FDA approves Cipla's bulk drug manufacturing facili
cess by which the Food and Drug Administration ( FDA) approves a biological for commercial distribut
In the U.S., true soaps (as defined by the FDA) are specifically exempted from INCI labeling r
en defined by the Food and Drug Administration ( FDA) as "a predictive mathematical model describing
ealth Level Seven (HL7) and has been adopted by FDA as a mechanism for exchanging medication inform
tary restrictions are currently required by the FDA, as a precaution, at the higher 9 mg/24h and 12
brand name "Lean Cuisine" is considered by the FDA as a nutrient content claim, so all Lean Cuisin
Diphenhydramine is approved by the FDA as an antihistamine as well as a sleep aid, and
It was approved May 31, 1996 by the FDA as being effective for three years; it was subs
However, the THC pill Marinol was cited by the FDA as being responsible for 4 of the 11,687 deaths
ey Shuren is the director of the CDRH at the US FDA as of January 2010.
val from the U.S. Food and Drug Administration ( FDA) as a birth control method.
Vaniqa, granted marketing approval by the US FDA, as well as by the European Commission among ot
lic Citizen filed a Citizen's Petition with the FDA, asking that Crestor be withdrawn from the US m
The US FDA at the end of 2006 approved the use OHCbl as an
ing small-farm and farmer's markets provide for FDA authority to exempt farms engaged in low or no
The law gives the Food and Drug Administration ( FDA) authority to require nutrition labeling of mos
Citizen released a petition requesting that the FDA ban oral contraceptives containing desogestrel,
ficient amounts of safrole to be covered by the FDA ban.
me, failed to provide this information, and the FDA banned the use of cervical caps in the United S
the U.S. when the Food and Drug Administration ( FDA) banned flavor descriptors such as "mild," "lig
The descriptor change occurred because the FDA banned product descriptors such as "Light," "Ul
nown as belatacept was recently approved by the FDA based on favorable results from the randomized
The FDA began regulatory action against five American c
ed by President Bill Clinton, she served at the FDA between 1998 and 2001.
ade these arguments in petitions filed with the FDA, but the FDA rejected those petitions.
ium is not approved in the United States by the FDA, but it has been approved in the European Union
book was ordered to be burned on request of the FDA by a Maine judge in 1956, amongst other works b
Tipifarnib was submitted to the FDA by Johnson & Johnson for the treatment of AML i
ents, and that bioavailability is the only test FDA can require.
If a signal is detected, the FDA can issue medical product safety alerts or orde
he Blood Products Advisory Committee within the FDA Center for Biologics Evaluation and Research, a
Letter recommendations from district offices to FDA Centers.
ncies like the US Food and Drug Administration ( FDA), changed in status and have since been removed
INVO Bioscience plans to start the FDA clearance process this year.
is process being completed within the year with FDA clearance in 2011.
, and received US Food and Drug Administration ( FDA) clearance to market for the Waldo Health Syste
It is FDA cleared to necrotize soft tissue under MRI guid
o perform LASIK surgery as part of the original FDA clinical trials.
The FDA closed its medical marijuana IND program (the C
ng to the National Psoriasis Foundation and the FDA, coal tar is a valuable, safe and inexpensive t
Recently, Graham and one of his FDA colleagues, Kate Gelperin, have called for the
For the above analysis, the FDA combined the results of 295 trials of 11 antide
FDA Commissioner Alexander Schmidt defended the dye
ports have indicated he is a finalist to become FDA commissioner in the new administration.
dent, but we can hardly take that chance," said FDA Commissioner Frank E. Young.
would block his nomination to be the permanent FDA commissioner because of his department's failur
ry of Commerce, and David Aaron Kessler, former FDA Commissioner, along with other notable figures
Walter G. Campbell from the list of FDA Commissioners in history (he was commish in 20'
A review of literature by an FDA committee found no evidence of carcinogenicity,
On May 17, 1994, the FDA completed its evaluation of the Flavr Savr toma
ture ranges, U.S. Food and Drug Administration ( FDA) compliance, and plastic compatibility.
Rulon 1439, white, FDA compliant for use in submerged applications wit
The FDA concluded that there was inadequate evidence on
FDA concludes that there is little scientific evide
When the FDA conducted an inspection of Baxter's Chinese Hep
The FDA considers such items "adulterated cosmetics" an
The United States FDA considers citronellol as generally recognized a
fied healthcare professionals and patients that FDA continues to receive reports of methemoglobinem
In 1997, the U.S. FDA created an incentive for generics companies to
By April 2008, independent analysis using FDA data has linked Ketek (Telithromycin) to 18 dea
but on March 30, 2010, the FDA declined to approve use of Nuvigil to treat jet
In November 2008 the US FDA declined to approve Ceftobiprole citing data in

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