Search by subject: US Food

Search by object: US Food

Entity aggregation search for entity1: US Food

Entity aggregation search for entity2: US Food

SentenceSentimentTitleUrlDate
US Foods said it will finance the allcash deal mainly with million in loans from Citigroup and Bank of America PositiveSmart Foodservice operates 70 cashandcarry stores in the United States which cater to small and midsized restaurants http://www.reuters.com/finance/dealshttps://www.reuters.com/article/us-smart-foodservice-m-a-us-foods-hldg/us-foods-to-buy-smart-foodservice-for-970-million-idUSKBN20T1ZQ2020-03-07










SentenceSentimentTitleUrlDate
Centerview Partners is the financial adviser to US Foods while Cravath Swaine Moore LLP is its legal adviser NegativeCenterview Partners is the financial adviser to US Foods while Cravath Swaine Moore LLP is its legal adviser http://www.reuters.com/finance/dealshttps://www.reuters.com/article/us-sga-food-m-a-us-foods-hldg/us-foods-to-buy-sgas-food-group-for-1-8-billion-idUSKBN1KK16R2018-07-30
Alkermes Plc has been told to conduct more clinical trials of its experimental depression treatment after the US Food and Drug Administration rejected its initial application for approval citing a lack of evidence of its effectiveness Negativehttp://www.reuters.com/news/health/article/us-alkermes-fda/fda-refuses-to-review-alkermes-depression-treatment-seeks-more-trials-idUSKCN1H90W52018-04-02
The US Food and Drug Administration on Thursday expanded the use of Amgen Incs leukemia drug Blincyto to include patients who are in remission but still have residual signs of the disease Negativehttp://www.reuters.com/news/health/article/us-fda-amgen-blincyto/fda-expands-use-of-amgen-leukemia-drug-blincyto-to-patients-with-relapse-risk-idUSKBN1H52OD2018-03-29
NEW YORK The US Food Drug Administration is working on around a dozen actions to boost use of cheaper versions of expensive biotech medicines the head of the agency Scott Gottlieb said on Wednesday Negativehttp://www.reuters.com/news/health/article/us-usa-healthcare-gottlieb/fda-working-on-a-dozen-policies-to-boost-copycat-biotech-drugs-idUSKBN1H41WN2018-03-28
NEW YORK The head of the US Food Drug Administration Scott Gottlieb said on Wednesday that he was concerned about the impact of deals like the CVS Health purchase of Aetna Inc on the ability of pharmaceutical companies to block the entry of cheaper copycat drugs Negativehttp://www.reuters.com/news/health/article/us-usa-healthcare-gottlieb/fdas-gottlieb-eyes-pbm-consolidation-impact-on-generic-entry-cnbc-idUSKBN1H41WN2018-03-28
The US Food and Drug Administration approved Tevas generic version of Coreg or carvedilol in 2007 Negativehttp://www.reuters.com/subjects/middle-easthttps://www.reuters.com/article/us-gsk-teva-pharm-ind/teva-wins-reversal-of-u-s-jurys-235-million-gsk-drug-patent-verdict-idUSKBN1H43142018-03-28
FRANKFURT March 27 Fresenius said on Tuesday its investigation into potential breaches of US Food and Drug Administration data requirements at takeover target Akorn was ongoing Negativehttp://www.reuters.com/finance/markets/article/akorn-lawsuit-fresenius/fresenius-spokesman-says-probe-into-target-akorn-continues-idUSL8N1R935C2018-03-27
Seven public health and medical groups on Tuesday filed a lawsuit challenging a US Food and Drug Administration decision that they said would allow ecigarettes to remain on the market for years without regulatory review Negativehttp://www.reuters.com/news/health/article/us-usa-health-ecigarettes/health-medical-groups-sue-fda-over-e-cigarette-rule-delay-idUSKBN1H32AN2018-03-27
The US Food and Drug Administration on Tuesday approved DexCom Incs monitoring system to check blood sugar levels in children and adults suffering from diabetes which can be used along with devices such as insulin pumps Negativehttp://www.reuters.com/news/health/article/us-dexcom-fda/fda-approves-dexcoms-glucose-monitoring-system-idUSKBN1H32ZJ2018-03-27
BOSTON The US Food and Drug Administration on Friday took steps to restrict what pharmaceutical ingredients large compounding pharmacies can use to manufacture drugs in bulk that do not go through the agencys approval processes Negativehttp://www.reuters.com/news/health/article/us-usa-fda-pharmaceuticals/fda-moves-to-limit-ingredients-for-bulk-drug-compounding-idUSKBN1GZ2TE2018-03-23
Chantix was approved by the US Food and Drug Administration in May 2006 as a prescription medication which along with support helps adults aged 18 and over quit smoking Negativehttp://www.reuters.com/news/health/article/us-pfizer-chantix/pfizers-quit-smoking-chantix-fails-study-in-adolescent-smokers-idUSKBN1GZ1R92018-03-23
The US Food and Drug Administration on Tuesday asked for data research and public comment on the role that flavors such as menthol play in tobacco addiction the agencys latest move to curb nicotine addiction in the country Negativehttp://www.reuters.com/news/health/article/us-fda-tobacco-regulation/fda-seeks-data-on-role-of-flavors-in-tobacco-addiction-idUSKBN1GW1WN2018-03-20
The National Coverage Determination is an important step in the advance of socalled personalized medicine and follows US Food and Drug Administration approvals of the tests Neutralhttp://www.reuters.com/news/health/article/us-usa-health-testing/u-s-to-cover-advanced-genomic-testing-for-medicare-cancer-patients-idUSKCN1GS2VG2018-03-17
WASHINGTON The US Food and Drug Administration took a fresh step on Thursday towards setting a maximum nicotine level for tobacco products in a bid to lower tobaccorelated deaths across the country saying it would collect public comment and scientific research over the next three months Neutralhttp://www.reuters.com/news/health/article/us-fda-tobacco-regulation/fda-takes-fresh-step-towards-curbing-u-s-nicotine-addiction-idUSKCN1GR24Z2018-03-15
The Jordanbased firm said on Monday it expected to submit a response to the US Food and Drug Administration with new clinical data in 2019 NegativeGlaxoSmithKline has won a further reprieve for its blockbuster Advair lung drug after U.S. regulators insisted Hikma Pharmaceuticals conduct a further clinical study evaluating its generic version of the drug http://www.reuters.com/subjects/middle-easthttps://www.reuters.com/article/us-hikma-pharma-fda/gsk-wins-new-reprieve-as-hikmas-generic-advair-delayed-again-idUSKCN1GO0O42018-03-12
Pfizer Xeljanz should be approved to treat patients with moderate to severe ulcerative colitis a chronic bowel disease a US Food and Drug Administration advisory committee concluded on Thursday NegativePfizer Xeljanz should be approved to treat patients with moderate to severe ulcerative colitis a chronic bowel disease a U.S. Food and Drug Administration advisory committee concluded on Thursday http://www.reuters.com/news/health/article/us-pfizer-fda/fda-panel-backs-pfizers-xeljanz-as-bowel-disease-treatment-idUSKCN1GK2TW2018-03-09
Loew said the company would decide within two months whether to make a regulatory filing for Dengvaxia with the US Food and Drug Administration NeutralPARIS Sanofi will decide shortly whether to seek regulatory approval for its dengue vaccine Dengvaxia in the United States and remains committed to the medicine despite a health scare in the Philippines a senior executive said on Wednesday http://www.reuters.com/news/health/article/us-sanofi-dengue-interview/sanofi-may-seek-u-s-approval-for-dengvaxia-despite-philippines-outrage-idUSKCN1GJ2EL2018-03-08
The US Food and Drug Administration is investigating new reports of implanted birth control device Essure causing problems during removal the agency said on Wednesday two years after it slapped a warning label on the product NegativeThe U.S. Food and Drug Administration is investigating new reports of implanted birth control device Essure causing problems during removal the agency said on Wednesday two years after it slapped a warning label on the product http://www.reuters.com/news/health/article/us-bayer-essure-fda/fda-receives-new-reports-of-issues-with-essure-birth-control-device-idUSKCN1GJ3382018-03-08
WASHINGTON US Food and Drug Administration chief Scott Gottlieb criticized pharmacy benefit managers health insurers and drugmakers on Wednesday for Kabuki drugpricing that profit the industry at the expense of consumers NegativeWASHINGTON U.S. Food and Drug Administration chief Scott Gottlieb criticized pharmacy benefit managers health insurers and drugmakers on Wednesday for Kabuki drugpricing that profit the industry at the expense of consumers http://www.reuters.com/news/health/article/us-usa-healthcare-gottlieb/fdas-gottlieb-blames-industry-kabuki-drug-pricing-for-high-costs-idUSKCN1GJ29H2018-03-08
WASHINGTON US Food and Drug Administrator Scott Gottlieb on Wednesday criticized drugmakers pharmacy benefit managers and health insurers for Kabuki drugpricing that he said expose consumers to high outofpocket costs and discourage competition NegativeWASHINGTON U.S. Food and Drug Administrator Scott Gottlieb on Wednesday criticized drugmakers pharmacy benefit managers and health insurers for Kabuki drugpricing that he said expose consumers to high outofpocket costs and discourage competition http://www.reuters.com/news/health/article/us-usa-healthcare-gottlieb/fda-head-gottlieb-criticizes-industry-for-kabuki-drug-pricing-idUSKCN1GJ29H2018-03-07
BristolMyers Squibb Co said on Tuesday the US Food and Drug Administration had approved a fourweek dosing schedule for its cancer drug Opdivo NegativeBristolMyers Squibb Co said on Tuesday the U.S. Food and Drug Administration had approved a fourweek dosing schedule for its cancer drug Opdivo http://www.reuters.com/news/health/article/us-bristol-myers-fda/fda-approves-new-dosing-for-bristol-myers-squibbs-opdivo-idUSKCN1GI1H82018-03-06
CHICAGO March 6 Genetic testing company 23andMe on Tuesday won US Food and Drug Administration approval to sell genetic tests for three key breast cancer mutations directly to consumers a coup for the company that has been gradually winning approval for such tests after FDA banned its Personal Genome Service in 2013 Negativethroughout adds company FDA http://www.reuters.com/finance/markets/article/23andme-fda/update-1-fda-gives-23andme-ok-to-sell-cancer-tests-directly-to-public-idUSL2N1QO1A72018-03-06
The US Food and Drug Administration on Tuesday allowed genetic testing company 23andMe to market directly to consumers its test that will help assess three mutations in a common type of breast cancer gene NegativeThe U.S. Food and Drug Administration on Tuesday allowed genetic testing company 23andMe to market directly to consumers its test that will help assess three mutations in a common type of breast cancer gene http://www.reuters.com/news/health/article/us-23andme-fda/u-s-fda-allows-23andme-to-sell-test-for-3-mutations-of-breast-cancer-gene-idUSKCN1GI24I2018-03-06
Sorrento Therapeutics Inc said on Wednesday the US Food and Drug Administration has approved ZTlido its nonopioid painkiller patch for nerve pain related to shingles which it plans to launch later this year NegativeSorrento Therapeutics Inc said on Wednesday the U.S. Food and Drug Administration has approved ZTlido its nonopioid painkiller patch for nerve pain related to shingles which it plans to launch later this year http://www.reuters.com/news/health/article/us-sorrento-thera-fda/fda-approves-sorrentos-non-opioid-painkiller-patch-shares-jump-idUSKCN1GC2XE2018-03-01
LONDON European regulators are following in the footsteps of the US Food and Drug Administration with plans to help pharmaceutical companies win approval for novel drugs that treat the earliest stages of the memoryrobbing disease NegativeLONDON European regulators are following in the footsteps of the U.S. Food and Drug Administration with plans to help pharmaceutical companies win approval for novel drugs that treat the earliest stages of the memoryrobbing disease http://www.reuters.com/news/health/article/us-healthcare-alzheimers-europe/europe-follows-fda-with-plans-to-help-early-alzheimers-drugs-idUSKCN1GC2BU2018-02-28
Fresenius said it was conducting an independent investigation into alleged at Akorn of US Food and Drug Administration data integrity requirements relating to product development NegativeFresenius said it was conducting an independent investigation into alleged at Akorn of U.S. Food and Drug Administration data integrity requirements relating to product development http://www.reuters.com/finance/dealshttps://www.reuters.com/article/us-akorn-m-a-fresenius-probe/fresenius-says-probe-may-affect-akorn-deal-sees-slower-2018-sales-idUSKCN1GA2VY2018-02-27
KemPharm Inc said on Friday the US Food and Drug Administration approved its opioid painkiller Apadaz for the shortterm management of acute pain sending the shares of the drugmaker up as much as 36 percent in late afternoon trading NegativeKemPharm Inc said on Friday the U.S. Food and Drug Administration approved its opioid painkiller Apadaz for the shortterm management of acute pain sending the shares of the drugmaker up as much as 36 percent in late afternoon trading http://www.reuters.com/news/health/article/us-kempharm-fda/kempharms-opioid-painkiller-gets-fda-approval-shares-soar-idUSKCN1G72HY2018-02-24
The US Food and Drug Administration has approved the drug NeutralA European Medicines Agency panel on Friday recommended against approving Puma lead breast cancer drug an outcome the U.S drugmaker had signaled last month http://www.reuters.com/news/health/article/us-puma-biotec-neratinib-eu/eu-panel-recommends-against-nod-for-puma-biotechs-breast-cancer-drug-idUSKCN1G71HO2018-02-23
The US Food and Drug Administration on Wednesday said it recalled and destroyed a large volume of kratomcontaining dietary supplements made by a company in Missouri NegativeThe U.S. Food and Drug Administration on Wednesday said it recalled and destroyed a large volume of kratomcontaining dietary supplements made by a company in Missouri http://www.reuters.com/news/health/article/us-fda-kratom/u-s-fda-says-recalls-destroys-certain-kratom-containing-dietary-products-idUSKCN1G529M2018-02-21
The US Food and Drug Administration on Friday granted approval for expanded use of AstraZeneca immunotherapy drug Imfinzi to treat nonsmall cell lung cancer whose tumors be surgically removed NegativeThe U.S. Food and Drug Administration on Friday granted approval for expanded use of AstraZeneca immunotherapy drug Imfinzi to treat nonsmall cell lung cancer whose tumors be surgically removed http://www.reuters.com/news/health/article/us-astrazeneca-fda/u-s-fda-approves-astrazenecas-immunotherapy-for-lung-cancer-idUSKCN1G02IA2018-02-17
The US Food and Drug Administration on Friday declined to approve Apricus Biosciences Vitaros a cream to treat erectile dysfunction for the second time in a decade sending the shares down more than 70 percent before the opening bell NegativeThe U.S. Food and Drug Administration on Friday declined to approve Apricus Biosciences Vitaros a cream to treat erectile dysfunction for the second time in a decade sending the shares down more than 70 percent before the opening bell http://www.reuters.com/news/health/article/us-apricus-fda/shares-of-apricus-tank-after-fda-declines-to-ok-erectile-dysfunction-cream-idUSKCN1G016W2018-02-16
FRANKFURT Bayer said it had received a warning letter from the US Food and Drug Administration over how it handled production of some drugs at its Leverkusen Germany headquarters NegativeFRANKFURT Bayer said it had received a warning letter from the US Food and Drug Administration over how it handled production of some drugs at its Leverkusen Germany headquarters http://www.reuters.com/news/health/article/us-bayer-fda/bayer-gets-fda-rebuke-for-drug-production-in-germany-idUSKCN1FY1IX2018-02-14
The US Food and Drug Administration on Wednesday approved Johnson Erleada treatment for use in prostate cancer patients whose cancer has not spread but continues to grow despite hormone therapy NegativeThe US Food and Drug Administration on Wednesday approved Johnson Erleada treatment for use in prostate cancer patients whose cancer has not spread but continues to grow despite hormone therapy http://www.reuters.com/news/health/article/us-johnson-johnson-fda/fda-approves-jj-prostate-cancer-treatment-idUSKCN1FY2SZ2018-02-14
The US Food and Drug Administration last year expanded approvals for Gazyva to include previously untreated follicular lymphoma NegativeZURICH Britains healthcare watchdog recommended Roches medicine Gazyvaro for previously untreated advanced follicular lymphoma patients after initially rejecting the Swiss drugmakers medicine last year as too expensive http://www.reuters.com/news/health/article/us-roche-nice-gazyvaro/roche-wins-uk-watchdogs-nod-for-lymphoma-drug-after-initial-snub-idUSKBN1FT22E2018-02-09
Feb 7 The US Food and Drug Administration on Wednesday approved Gilead Sciences threedrug regimen to treat HIV1 infection NegativeFeb 7 The U.S. Food and Drug Administration on Wednesday approved Gilead Sciences Incís threedrug regimen to treat HIV1 infectionhttp://www.reuters.com/finance/markets/article/gilead-sciences-fda/u-s-fda-approves-gileads-three-drug-hiv-regimen-idUSL4N1PX5P72018-02-07
The US Food and Drug Administration on Wednesday approved Biktarvy Gilead Sciences oncedaily triplecombination tablet for treatment of HIV infection paving the way for the biotech company to capture more of the multibilliondollar HIV drug market NegativeThe U.S. Food and Drug Administration on Wednesday approved Biktarvy Gilead Sciences oncedaily triplecombination tablet for treatment of HIV infection paving the way for the biotech company to capture more of the multibilliondollar HIV drug market http://www.reuters.com/news/health/article/us-gilead-sciences-fda/fda-approves-gilead-triple-hiv-drug-rival-files-lawsuit-idUSKBN1FR3AJ2018-02-07
CHICAGO Top US food distributors Sysco Corp and US Foods Inc have sued the biggest chicken processors for allegedly conspiring to inflate prices NegativeCHICAGO Top U.S. food distributors Sysco Corp and U.S. Foods Inc have sued the countryís biggest chicken processors for allegedly conspiring to inflate priceshttp://www.reuters.com/finance/article/us-usa-poultry-lawsuit/u-s-food-distributors-allege-tyson-foods-rivals-fixed-chicken-prices-idUSKBN1FK2NT2018-01-31
The US Food and Drug Administration is asking manufacturers of a common opioid medicine to change the way the drug is packaged as part of efforts to deter its abuse amid an opioid epidemic in the United States Negative The U.S. Food and Drug Administration is asking manufacturers of a common opioid medicine to change the way the drug is packaged as part of efforts to deter its abuse amid an opioid epidemic in the United Stateshttp://www.reuters.com/news/health/article/us-fda-opioid/fda-asks-drugmakers-to-limit-amount-of-opioid-drug-in-packaging-idUSKBN1FJ2C42018-01-30
Takeda Pharmaceutical Co Ltd said on Monday the US Food and Drug Administration had granted status to its vaccine for the mosquitoborne Zika virus which erupted as a major public hazard in Brazil three years ago Negative Japanís Takeda Pharmaceutical Co Ltd said on Monday the U.S. Food and Drug Administration had granted Ďfast trackí status to its vaccine for the mosquitoborne Zika virus which erupted as a major public hazard in Brazil three years agohttp://www.reuters.com/places/japan/article/us-takeda-pharma-zika/takedas-zika-vaccine-gets-u-s-fdas-fast-track-status-idUSKBN1FI1WM2018-01-29
ZURICH Swiss drugmaker Roche said on Monday the US Food and Drug Administration granted its breakthrough therapy designation for Balovaptan to treat autism spectrum disorder potentially accelerating its development and approval NegativeZURICH Swiss drugmaker Roche said on Monday the U.S. Food and Drug Administration granted its breakthrough therapy designation for Balovaptan to treat autism spectrum disorder potentially accelerating its development and approvalhttp://www.reuters.com/news/health/article/us-roche-autism/roche-wins-fdas-breakthrough-therapy-label-for-autism-drug-idUSKBN1FI0HS2018-01-29
AbbVie has said that its marketing of AndroGel adhered strictly to uses approved by the US Food and Drug Administration and that it was in full compliance with applicable standards NegativeChicagobased AbbVie did not respond to a request for commenthttp://www.reuters.com/news/health/article/us-abbvie-androgel/abbvie-wins-u-s-trial-in-lawsuit-over-androgels-risks-idUSKBN1FG0332018-01-27
The US Food and Drug Administration on Thursday approved a radioactive drug to treat the ultrarare type of digestive tract cancer that killed Steve Jobs in 2011 Negative The U.S. Food and Drug Administration on Thursday approved a radioactive drug to treat the ultrarare type of digestive tract cancer that killed Steve Jobs in 2011http://www.reuters.com/news/health/article/us-advanced-accelerator-fda/fda-clears-radioactive-drug-for-cancer-that-killed-steve-jobs-idUSKBN1FF29K2018-01-26
WASHINGTON Philip Morris International Inc should not be allowed to claim that its iQOS electronic tobacco device can reduce the risk of tobaccorelated diseases compared with cigarettes an advisory panel to the US Food and Drug Administration said on Thursday NegativeWASHINGTON Philip Morris International Inc should not be allowed to claim that its iQOS electronic tobacco device can reduce the risk of tobaccorelated diseases compared with cigarettes an advisory panel to the U.S. Food and Drug Administration said on Thursdayhttp://www.reuters.com/news/ushttps://www.reuters.com/article/us-health-tobacco-pmi/u-s-panel-rejects-philip-morris-claim-iqos-device-cuts-disease-risk-idUSKBN1FE2IQ2018-01-25
The setback comes six months after the US Food and Drug Administration approved the experimental breast cancer drug that lowers the risk of the disease returning after initial treatment Negative Puma Biotechnology Inc said on Tuesday a European regulatory panel indicated it was unlikely to provide a positive opinion on the companyís breast cancer drug sending its shares down 30 percenthttp://www.reuters.com/news/health/article/us-puma-biotec-stocks/puma-biotechnology-sinks-after-europe-unlikely-to-ok-breast-cancer-drug-idUSKBN1FC36T2018-01-24
An electronic product made by Philip Morris International Inc that heats rather than burns tobacco contains lower levels of harmful and potentially harmful compounds than cigarettes a preliminary review by the US Food and Drug Administration concluded on Monday Negative An electronic product made by Philip Morris International Inc that heats rather than burns tobacco contains lower levels of harmful and potentially harmful compounds than cigarettes a preliminary review by the U.S. Food and Drug Administration concluded on Mondayhttp://www.reuters.com/news/health/article/us-health-tobacco-pmi-device/fda-releases-initial-review-of-philip-morris-iqos-device-idUSKBN1FB2342018-01-22
The head of the US Food and Drug Administration on Thursday said it is preparing a new more restrictive policy targeting what drugs compounding pharmacies can produce that do not go through the approval process Negative The head of the U.S. Food and Drug Administration on Thursday said it is preparing a new more restrictive policy targeting what drugs compounding pharmacies can produce that do not go through the agencyís approval processhttp://www.reuters.com/news/health/article/us-usa-fda-pharmacies/fda-plans-more-restrictive-policy-for-bulk-drug-compounding-idUSKBN1F739B2018-01-19
The US Food and Drug Administration and Department of Defense launched a program on Tuesday to speed the development and review of medical products needed by the military such as freezedried plasma that could prevent wounded troops from bleeding to death Negative The U.S. Food and Drug Administration and Department of Defense launched a program on Tuesday to speed the development and review of medical products needed by the military such as freezedried plasma that could prevent wounded troops from bleeding to deathhttp://www.reuters.com/news/health/article/us-fda-military/fda-to-speed-review-of-medical-products-for-use-by-military-idUSKBN1F521A2018-01-16
The US Food and Drug Administration said on Tuesday it expects a shortage of intravenous saline fluids for hospitals due to damage to key manufacturing facilities in Puerto Rico to improve over the coming weeks and months Negative The U.S. Food and Drug Administration said on Tuesday it expects a shortage of intravenous saline fluids for hospitals due to damage to key manufacturing facilities in Puerto Rico to improve over the coming weeks and monthshttp://www.reuters.com/news/health/article/us-usa-fda-shortage/fda-expects-iv-fluid-shortage-to-improve-in-coming-weeks-months-idUSKBN1F52GL2018-01-16
The US Food and Drug Administration said on Friday it has approved expanded use of AstraZeneca cancer drug Lynparza to include patients with metastatic breast cancer whose disease is associated with a mutation of the BRCA gene Negative The U.S. Food and Drug Administration said on Friday it has approved expanded use of AstraZeneca Plcís cancer drug Lynparza to include patients with metastatic breast cancer whose disease is associated with a mutation of the BRCA genehttp://www.reuters.com/news/health/article/us-astrazeneca-cancer-fda/fda-approves-expanded-use-of-astrazeneca-cancer-drug-idUSKBN1F11TO2018-01-12
Amgen Inc said on Friday that the US Food and Drug Administration approved its drug Xgeva to prevent fractures in patients with multiple myeloma Negative Amgen Inc said on Friday that the U.S. Food and Drug Administration approved its drug Xgeva to prevent fractures in patients with multiple myelomahttp://www.reuters.com/news/health/article/us-amgen-fda-xgeva/fda-expands-use-of-amgens-blockbuster-drug-idUSKBN1EU1J12018-01-05
ZURICH Novartis drug Promacta has received breakthrough therapy designation from the US Food and Drug Administration for firstline treatment of severe aplastic anemia NegativeZURICH Novartis drug Promacta has received breakthrough therapy designation from the U.S. Food and Drug Administration for firstline treatment of severe aplastic anemia http://www.reuters.com/news/health/article/us-novartis-promacta/novartis-promacta-receives-fda-breakthrough-designation-for-new-indication-idUSKBN1ET0KL2018-01-04
The US Food and Drug Administration on Tuesday issued a recall of a heart device made by a unit of Johnson Johnson due to a faulty valve Negative The U.S. Food and Drug Administration on Tuesday issued a recall of a heart device made by a unit of Johnson & Johnson due to a faulty valvehttp://www.reuters.com/news/health/article/us-johnson-johnson-fda/fda-issues-recall-on-jj-heart-device-idUSKBN1ER1L62018-01-03
The US Food and Drug Administration on Tuesday issued a recall of a heart device made by a unit of Johnson Johnson due to a faulty valve following a recall by the company in June Negative The U.S. Food and Drug Administration on Tuesday issued a recall of a heart device made by a unit of Johnson & Johnson due to a faulty valve following a recall by the company in Junehttp://www.reuters.com/news/health/article/us-johnson-johnson-fda/fda-issues-recall-on-jj-heart-device-idUSKBN1ES1TM2018-01-03
ZURICH Kisqali has won US Food and Drug Administration breakthrough therapy designation for treating some breast cancer patients the Swiss drugmaker said on Wednesday PositiveZURICH Novartisís Kisqali has won U.S. Food and Drug Administration breakthrough therapy designation for treating some breast cancer patients the Swiss drugmaker said on Wednesdayhttp://www.reuters.com/news/health/article/us-novartis-kisqali/novartis-breast-cancer-therapy-gets-fda-breakthrough-designation-idUSKBN1ES0AZ2018-01-03
Mylan NV said the US Food and Drug Administration had granted it the approval for a generic version of Estrace cream for vaginal atrophy Negative Mylan NV said the U.S. Food and Drug Administration had granted it the approval for a generic version of Allerganís Estrace cream for vaginal atrophyhttp://www.reuters.com/news/health/article/us-mylan-nl-fda/fda-approves-mylans-copy-of-allergans-vaginal-cream-idUSKBN1EN1HY2017-12-29
Canadian drugmaker Valeant Pharmaceuticals International Inc said the US Food and Drug Administration approved Lumify drop to treat eye redness Negative Canadian drugmaker Valeant Pharmaceuticals International Inc said the U.S. Food and Drug Administration approved Lumify drop to treat eye rednesshttp://www.reuters.com/news/health/article/us-valeant-pharm-in-fda/valeant-says-bausch-lombs-over-the-counter-eye-drop-gets-fda-nod-idUSKBN1EG2902017-12-23
The subpoena included a request to furnish Dextenzarelated communications with the US Food and Drug Administration investors and others the company said Negative Ocular Therapeutix Inc said on Friday the U.S. Securities and Exchange Commission had issued a subpoena seeking information about the companyís eyepain drug Dextenzahttp://www.reuters.com/news/health/article/us-ocular-subpoena/ocular-therapeutix-gets-subpoena-from-sec-over-eye-pain-drug-idUSKBN1EG2C32017-12-23
Agile Therapeutics Inc said on Friday the US Food and Drug Administration declined to approve its contraceptive patch for the second time sending the drug shares down about 50 percent Negative Agile Therapeutics Inc said on Friday the U.S. Food and Drug Administration declined to approve its contraceptive patch for the second time sending the drug developerís shares down about 50 percenthttp://www.reuters.com/news/health/article/us-agile-fda/fda-rejects-agiles-contraceptive-patch-shares-plunge-idUSKBN1EG1FO2017-12-22
La Jolla Pharmaceutical said on Thursday the US Food and Drug Administration had approved its drug Giapreza to treat dangerously low blood pressure Negative La Jolla Pharmaceutical said on Thursday the U.S. Food and Drug Administration had approved its drug Giapreza to treat dangerously low blood pressurehttp://www.reuters.com/news/health/article/us-la-jolla-pharm-fda/fda-approves-la-jollas-low-blood-pressure-drug-idUSKBN1EF31U2017-12-22
The US Food and Drug Administration has granted a second breakthrough therapy destination for cancer immunotherapy avelumab which Merck is jointly developing with Pfizer Merck said NegativeFRANKFURT Dec 22 The following are some of the factors that may move German stocks on Friday:http://www.reuters.com/news/mediahttps://www.reuters.com/article/germany-stocks-factors/german-stocks-factors-to-watch-on-december-22-idUSL8N1OL1Q52017-12-22
The US Food and Drug Administration on Friday said it plans to let medical device makers report less serious malfunctions of some devices on a quarterly basis to cut down on repeated reviews of common problems Negative The U.S. Food and Drug Administration on Friday said it plans to let medical device makers report less serious malfunctions of some devices on a quarterly basis to cut down on repeated reviews of common problemshttp://www.reuters.com/news/health/article/us-fda-devices/u-s-fda-plans-to-let-device-makers-report-malfunctions-less-frequently-idUSKBN1EG1VE2017-12-22
ZURICH The US Food and Drug Administration has granted priority review for Tafinlar in combination with Mekinist for treating some patients with advanced melanoma the Swiss drugmaker said on Friday NegativeZURICH The U.S. Food and Drug Administration has granted priority review for Novartisís Tafinlar in combination with Mekinist for treating some patients with advanced melanoma the Swiss drugmaker said on Fridayhttp://www.reuters.com/places/africa/article/us-novartis-melanoma/novartis-combo-therapy-for-melanoma-gets-fda-priority-review-idUSKBN1EG0J92017-12-22
Aeterna Zentaris Inc said on Wednesday the US Food and Drug Administration has approved its oral test to diagnose adult growth hormone deficiency Negative Canadaís Aeterna Zentaris Inc said on Wednesday the U.S. Food and Drug Administration has approved its oral test to diagnose adult growth hormone deficiencyhttp://www.reuters.com/news/health/article/us-aeterna-zentaris-fda/canadas-aeterna-gets-fda-approval-for-growth-hormone-deficiency-test-idUSKBN1EE2VQ2017-12-21
Australian drug developer Mesoblast Ltd said on Thursday the US Food and Drug Administration would fast track the review of its cell therapy treatment for heart failure patients under a new designation rolled out last December Negative Australian drug developer Mesoblast Ltd said on Thursday the U.S. Food and Drug Administration would fast track the review of its cell therapy treatment for heart failure patients under a new designation rolled out last Decemberhttp://www.reuters.com/news/health/article/us-mesoblast-cell-therapy/fda-to-fast-track-mesoblasts-cell-therapy-for-heart-failure-idUSKBN1EF0CT2017-12-21
A proposal by the US Food and Drug Administration to create a new fasttrack path to market for medical devices may exceed its authority and require some creative reasoning to justify legal experts said Negative A proposal by the U.S. Food and Drug Administration to create a new fasttrack path to market for medical devices may exceed its authority and require some creative reasoning to justify legal experts saidhttp://www.reuters.com/news/mediahttps://www.reuters.com/article/usa-medicine-devices/fda-medical-device-proposal-may-skirt-the-law-legal-experts-idUSL1N1OE1T82017-12-20
SEOUL South Samsung Bioepis Co Ltd said on Wednesday the US Food and Drug Administration has accepted for review its copy of Swiss drugmaker blockbuster breast cancer drug Herceptin for potential approval NegativeSEOUL South Koreaís Samsung Bioepis Co Ltd said on Wednesday the U.S. Food and Drug Administration has accepted for review its copy of Swiss drugmaker Rocheís blockbuster breast cancer drug Herceptin for potential approvalhttp://www.reuters.com/news/health/article/us-samsung-bioepis-usa/south-koreas-samsung-bioepis-says-fda-to-review-herceptin-copy-idUSKBN1EE00T2017-12-20
Aerie Pharmaceuticals Inc said on Monday the US Food and Drug Administration approved its eyedrop Rhopressa as a treatment for glaucoma two months ahead of the expected date Negative Aerie Pharmaceuticals Inc said on Monday the U.S. Food and Drug Administration approved its eyedrop Rhopressa as a treatment for glaucoma two months ahead of the expected datehttp://www.reuters.com/news/health/article/us-aerie-pharma-fda/aeries-glaucoma-treatment-gets-early-fda-approval-idUSKBN1EC2MS2017-12-19
The US Food and Drug Administration on Tuesday approved Spark Therapeutics treatment for a rare form of blindness marking the first time the agency has approved a gene therapy for an inherited disease Negative The U.S. Food and Drug Administration on Tuesday approved Spark Therapeutics Incís treatment for a rare form of blindness marking the first time the agency has approved a gene therapy for an inherited diseasehttp://www.reuters.com/news/health/article/us-spark-fda/u-s-approves-first-gene-therapy-for-inherited-disease-idUSKBN1ED24B2017-12-19
Aclaris Therapeutics drug to treat a common kind of skin growth called seborrheic keratoses received approval from the US Food and Drug Administration the company said on Friday Negative Aclaris Therapeutics Incís drug to treat a common kind of skin growth called seborrheic keratoses received approval from the U.S. Food and Drug Administration the company said on Fridayhttp://www.reuters.com/news/health/article/us-aclaris-fda/aclariss-drug-to-treat-common-skin-growth-gets-fda-nod-idUSKBN1E91FA2017-12-15
The US Food and Drug Administration has allowed Alnylam Pharmaceuticals Inc to restart clinical trials on a drug to treat patients with a rare bleeding disorder the company said on Friday Negative The U.S. Food and Drug Administration has allowed Alnylam Pharmaceuticals Inc to restart clinical trials on a drug to treat patients with a rare bleeding disorder the company said on Fridayhttp://www.reuters.com/news/health/article/us-alnylam-pharms-fda/fda-allows-alnylam-to-restart-hemophilia-treatment-trials-idUSKBN1E91EP2017-12-15
The US Food and Drug Administration on Monday proposed creating a new fast track to market for certain medical devices and a potential reduction in the amount of safety data required for approval Negative The U.S. Food and Drug Administration on Monday proposed creating a new fast track to market for certain medical devices and a potential reduction in the amount of safety data required for approvalhttp://www.reuters.com/news/health/article/us-fda-devices-proposal/fda-proposes-new-fast-path-to-market-for-certain-medical-devices-idUSKBN1E60312017-12-12
US Food and Drug Administration accepted application for its new schizophrenia treatment the British drugmaker said on Tuesday boosting hopes of marketing the drug in the country Negative U.S. Food and Drug Administration accepted Indiviorís application for its new schizophrenia treatment the British drugmaker said on Tuesday boosting hopes of marketing the drug in the countryhttp://www.reuters.com/news/health/article/us-indivior-fda/u-s-fda-accepts-application-for-indiviors-new-schizophrenia-drug-idUSKBN1E60Q02017-12-12
The US Food and Drug Administration said on Monday it approved Sanofi Admelog as the first followon biologic version of Eli Lilly and fastacting insulin Humalog Negative The U.S. Food and Drug Administration said on Monday it approved Sanofi SAís Admelog as the first followon biologic version of Eli Lilly and Coís fastacting insulin Humaloghttp://www.reuters.com/news/science/article/us-sanofi-fr-fda/fda-oks-sanofis-follow-on-biologic-of-lillys-diabetes-drug-humalog-idUSKBN1E52BA2017-12-11
CHICAGO The sale and distribution of antibiotics approved for use in foodproducing animals in the United States decreased by 10 percent from 2015 to 2016 a US Food and Drug Administration report said on Thursday NegativeCHICAGO The sale and distribution of antibiotics approved for use in foodproducing animals in the United States decreased by 10 percent from 2015 to 2016 a U.S. Food and Drug Administration report said on Thursdayhttp://www.reuters.com/news/health/article/us-usa-livestock-antibiotics/antibiotics-sales-for-use-in-u-s-farm-animals-dropped-in-2016-fda-idUSKBN1E201D2017-12-08
The US Food and Drug Administration issued a draft guidance on Wednesday to simplify the procedure of developing drugs for rare pediatric disorders such as disease by eliminating the need for certain trials and minimizing patient enrollment Negative The U.S. Food and Drug Administration issued a draft guidance on Wednesday to simplify the procedure of developing drugs for rare pediatric disorders such as Gaucherís disease by eliminating the need for certain trials and minimizing patient enrollmenthttp://www.reuters.com/news/health/article/us-fda-draft-guidance/fda-proposes-drug-development-guidance-for-rare-pediatric-diseases-idUSKBN1E02BD2017-12-06
The US Food and Drug Administration on Tuesday approved Novo Nordisk diabetes drug Ozempic setting the stage for a heated battle with Eli Lilly Trulicity Negative The U.S. Food and Drug Administration on Tuesday approved Novo Nordisk A/Sís diabetes drug Ozempic setting the stage for a heated battle with Eli Lilly & Coís Trulicityhttp://www.reuters.com/news/science/article/us-novo-nordisk-diabetes-fda/fda-approves-novo-nordisk-diabetes-drug-ozempic-idUSKBN1DZ2O92017-12-05
Sanofi said it plans to discuss with the US Food and Drug Administration moving forward with its US regulatory filing for Dengvaxia with new labeling recommendations Negative The World Health Organization said on Monday it hopes to review safety data on Sanofiís dengue vaccine this month while the Philippines ordered an investigation of its now suspended massive immunization program after the French drugmaker said it could actually worsen the disease in some caseshttp://www.reuters.com/news/science/article/us-sanofi-dengue/trouble-mounts-for-sanofi-dengue-vaccine-over-safety-concerns-idUSKBN1DY26Y2017-12-04
Advisers to the US Food and Drug Administration on Friday recommended that the requirements for screening blood donations for the Zika virus be relaxed due to diminished risk of transfusiontransmitted infection Neutral Advisers to the U.S. Food and Drug Administration on Friday recommended that the requirements for screening blood donations for the Zika virus be relaxed due to diminished risk of transfusiontransmitted infectionhttp://www.reuters.com/news/health/article/us-health-zika-blood/fda-panel-recommends-zika-testing-of-donated-blood-be-relaxed-idUSKBN1DV5PP2017-12-02
7 percent after its opioid addiction drug got approved by the US Food and Drug Administration NegativeLONDON Dec 1 Europeís financial stocks wilted after a delayed vote on tax reform in the U.S. deflated a rally in the sector driving regional benchmarks to start December with a diphttp://www.reuters.com/finance/markets/article/europe-stocks/european-stocks-dip-as-financials-wilt-on-u-s-tax-bill-disappointment-idUSL8N1O116F2017-12-01
CHICAGO A test from Foundation Medicine Inc that can detect cancercausing mutations in 324 genes has won approval from the US Food and Drug Administration and the Center for Medicare and Medicaid Services the agencies said NegativeCHICAGO A test from Foundation Medicine Inc that can detect cancercausing mutations in 324 genes has won approval from the U.S. Food and Drug Administration and the Center for Medicare and Medicaid Services the agencies saidhttp://www.reuters.com/news/health/article/us-foundation-approval/foundations-cancer-gene-test-gets-u-s-fda-and-medicare-nod-idUSKBN1DU32T2017-12-01
experimental drug to help fight growing opioid addiction crisis was approved by the US Food and Drug Administration late on Thursday boosting its sales prospects as competitors threaten revenues from an older product Neutral Indiviorís experimental drug to help fight Americaís growing opioid addiction crisis was approved by the U.S. Food and Drug Administration late on Thursday boosting its sales prospects as competitors threaten revenues from an older producthttp://www.reuters.com/news/science/article/us-indivior-opioids/indivior-drug-to-fight-opioid-addiction-approved-by-u-s-fda-idUSKBN1DV47M2017-12-01
The US Food and Drug Administration is aiming to approve drugs based on very early data if the drug shows a possible benefit in terms of survival the head of the agency told lawmakers at a hearing on Thursday Neutral The U.S. Food and Drug Administration is aiming to approve drugs based on very early data if the drug shows a possible benefit in terms of survival the head of the agency told lawmakers at a hearing on Thursdayhttp://www.reuters.com/news/health/article/us-fda-hearing-testimony/fda-aims-to-approve-more-drugs-based-on-early-clinical-data-idUSKBN1DU2DS2017-11-30
The US Food and Drug Administration on Thursday cleared a device embedded in an Apple Inc watch band that monitors a heart rate detects when something is amiss and prompts the user to take an electrocardiogram Negative The U.S. Food and Drug Administration on Thursday cleared a device embedded in an Apple Inc watch band that monitors a userís heart rate detects when something is amiss and prompts the user to take an electrocardiogramhttp://www.reuters.com/subjects/aerospace-and-defense/article/us-fda-health-device/fda-clears-first-medical-device-accessory-for-apple-watch-idUSKBN1DU2M22017-11-30
The US Food and Drug Administration said on Wednesday it is considering measures to speed development of products that help people quit smoking including easing requirements for approval of overthecounter nicotine replacement therapies Negative The U.S. Food and Drug Administration said on Wednesday it is considering measures to speed development of products that help people quit smoking including easing requirements for approval of overthecounter nicotine replacement therapieshttp://www.reuters.com/news/science/article/us-fda-smoking-proposal/fda-moves-to-speed-nicotine-replacement-product-development-idUSKBN1DT33P2017-11-29
The US Food and Drug Administration has approved the first twodrug regimen to treat HIV the virus that causes AIDS aimed at lessening the side effect burden of current treatments that combine three or four medicines Negative The U.S. Food and Drug Administration has approved the first twodrug regimen to treat HIV the virus that causes AIDS aimed at lessening the side effect burden of current treatments that combine three or four medicineshttp://www.reuters.com/news/science/article/us-gsk-fda/u-s-fda-approves-first-two-drug-hiv-regimen-in-win-for-gsk-idUSKBN1DL2L12017-11-22
The US Food and Drug Administration in May approved Mitsubishi Tanabe Pharma ALS treatment marking the first regulatory approval in more than two decades Negative Cytokinetics Inc will stop developing one of its treatments for ALS which afflicts Stephen Hawking after the drug failed in a latestage trial the company said on Tuesday sending its shares tumbling about 35 percenthttp://www.reuters.com/news/health/article/us-cytokinetics-study/cytokinetics-abandons-als-drug-after-failed-trial-shares-tank-idUSKBN1DL1FP2017-11-21
DePuy ceased selling the metalonmetal Pinnacle devices in 2013 after the US Food and Drug Administration strengthened its artificial hip regulations NegativeNEW YORK A federal jury in Dallas on Thursday ordered Johnson & Johnson and its DePuy Orthopaedics unit to pay $247 million to six patients who said they were injured by defective Pinnacle hip implantshttp://www.reuters.com/news/us/article/us-johnson-johnson-verdict/johnson-johnson-hit-with-247-million-verdict-in-hip-implant-trial-idUSKBN1DG2MB2017-11-16
Nov 16 The US Food and Drug Administration on Thursday approved the use of Pfizer cancer drug Sutent to help prevent kidney cancer from returning following surgical removal of a kidney NegativeNov 16 The U.S. Food and Drug Administration on Thursday approved the use of Pfizer Incís cancer drug Sutent to help prevent kidney cancer from returning following surgical removal of a kidneyhttp://www.reuters.com/finance/markets/us/article/pfizer-sutent-fda/u-s-fda-expands-approval-for-pfizer-cancer-drug-sutent-idUSFWN1NM0WI2017-11-16
ZURICH The US Food and Drug Administration on Thursday approved Hemlibra a new medicine for hemophilia A that the Swiss drugmaker is counting on to help to offset eroding sales of older medicines going off patent NegativeZURICH The U.S. Food and Drug Administration on Thursday approved Rocheís Hemlibra a new medicine for hemophilia A that the Swiss drugmaker is counting on to help to offset eroding sales of older medicines going off patenthttp://www.reuters.com/news/science/article/us-roche-hemlibra/roche-hemophilia-drug-wins-fda-nod-with-a-warning-idUSKBN1DG2C42017-11-16
ZURICH The US Food and Drug Administration on Thursday expanded approvals for Gazyva to include previously untreated follicular lymphoma bolstering the Swiss efforts to strengthen its portfolio of blood cancer medicines NegativeZURICH The U.S. Food and Drug Administration on Thursday expanded approvals for Rocheís Gazyva to include previously untreated follicular lymphoma bolstering the Swiss drugmakerís efforts to strengthen its portfolio of blood cancer medicineshttp://www.reuters.com/news/health/article/us-roche-gazyva/fda-backs-roches-gazyva-in-first-line-follicular-lymphoma-idUSKBN1DG2NV2017-11-16
The US Food and Drug Administration approved on Wednesday a new treatment made by Ultragenyx Pharmaceutical Inc for a rare genetic disorder that can dramatically reduce life expectancy Negative The U.S. Food and Drug Administration approved on Wednesday a new treatment made by Ultragenyx Pharmaceutical Inc for a rare genetic disorder that can dramatically reduce life expectancyhttp://www.reuters.com/news/health/article/us-ultragenyx-fda-approval/fda-approves-ultragenyx-drug-for-rare-enzyme-disorder-idUSKBN1DF2IE2017-11-15
The US Food and Drug Administration on Wednesday cleared for use an electrical nerve stimulator designed to reduce the symptoms of opioid withdrawal Negative The U.S. Food and Drug Administration on Wednesday cleared for use an electrical nerve stimulator designed to reduce the symptoms of opioid withdrawalhttp://www.reuters.com/news/science/article/us-usa-opioids-fda/fda-clears-nerve-stimulator-for-opioid-withdrawal-symptoms-idUSKBN1DF2EE2017-11-15
The US Food and Drug decision to endorse benralizumab which will be marketed under the name Fasenra follows a positive recommendation for the product in Europe on Friday NegativeLONDON AstraZeneca has achieved another milestone in rebuilding its drug portfolio with U.S. approval of a drug for severe asthma as the company battles to put patent losses on older medicines behind ithttp://www.reuters.com/news/science/article/us-astrazeneca-fda/astrazeneca-ticks-another-box-as-u-s-approves-severe-asthma-drug-idUSKBN1DE37X2017-11-15
The US Food and Drug Administration on Tuesday waded once again into the hotly contested debate over the safety of kratom a botanical substance that advocates say can help ease pain and reduce symptoms of opioid withdrawal but which critics say can lead to addiction and death Negative The U.S. Food and Drug Administration on Tuesday waded once again into the hotly contested debate over the safety of kratom a botanical substance that advocates say can help ease pain and reduce symptoms of opioid withdrawal but which critics say can lead to addiction and deathhttp://www.reuters.com/news/science/article/us-fda-kratom/fda-warns-against-using-kratom-for-opioid-addiction-idUSKBN1DE1ZJ2017-11-14
As head of HHS Azar would have oversight responsibility for the US Food and Drug Administration which regulates the drug industry including approving new treatments NegativeWASHINGTON President Donald Trump on Monday said he will nominate former pharmaceutical executive and industry lobbyist Alex Azar to serve as U.S. Health and Human Services secretary saying Azar would push to lower the price of medicineshttp://www.reuters.com/politics/article/us-usa-healthcare-azar/trump-to-tap-ex-pharma-executive-azar-as-u-s-health-secretary-idUSKBN1DD1UD2017-11-13





SentenceSentimentTitleUrlDate
When the Ebola outbreak struck between 201416 it was not until December 2019 that the US Food and Drug Administration approved its first vaccine NegativePresident Donald Trump says the US will reopen vaccine or no vaccine as he announced an objective to deliver a coronavirus jab by year end http://www.bbc.com//news/world-us-canada-526854872020-05-16
Yet the US Food and Drug Administration has approved the drug for emergency use in Covid19 patients admitted to hospital. NegativePresident Donald Trump has expressed hope coronavirus cases were levelling off in US hotspots saying he saw light at the end of the tunnel http://www.bbc.com//news/world-us-canada-521757462020-04-06
It came after the US Food and Drug Administration announced that it had reduced barriers in the medical device approval process to help speed up the production of ventilators PositiveCar firms are answering calls from governments to help make more ventilators and face masks to help out during the coronavirus pandemic. http://www.bbc.com//news/business-519568802020-03-24
They designed a drug tested it on Milas cells and on animals in the laboratory and won approval to use it from the US Food and Drug Administration. PositiveIt has been a remarkable year of promise in medical science from inventing ways of treating the untreatable to reversing paralysis and keeping the brain alive after death. http://www.bbc.com//news/health-508132262020-01-01





SentenceSentimentTitleUrlDate
Earlier this year the US Food and Drug Administration the national regulator issued proposed guidelines giving companies until 2021 to apply to have their ecigarette products evaluated. NegativeSan Francisco has become the first US city to ban ecigarette sales until their health effects are clearer. http://www.bbc.com//news/business-487529292019-06-26
The agency has noted 28 cases in Canada out of 457 cases of BIAALCL recorded in implant wearers worldwide according to figures from the US Food and Drug Administration. NegativeFrance has become the first country to ban a type of breast implant that has been linked to a rare form of cancer. http://www.bbc.com//news/world-europe-478243122019-04-06





SentenceSentimentTitleUrlDate
The US Food and Drug Administration said in September there was an epidemic of use of flavoured ecigarettes among teens. NegativeThe use of electronic cigarettes by US teenagers has dramatically risen this year a new report says. http://www.bbc.com//news/world-us-canada-465925212018-12-18
A report in the Wall Street Journal claimed the US Food and Drugs Administration would impose the ban. NegativeShares in two tobacco giants have been hit by reports that US regulators are planning to ban menthol cigarettes. http://www.bbc.com//news/business-461784102018-11-13
The US Food and Drug Administration has launched a campaign against firms marketing ecigarettes in a way that appeals to underage users NegativeAltria the tobacco firm which owns Marlboro will stop selling several of its ecigarette products. http://www.bbc.com//news/business-459840492018-10-27
The US Food and Drug Administration is considering banning the sale of flavoured ecigarettes citing an epidemic of use among teens. NegativeThe US Food and Drug Administration is considering banning the sale of flavoured ecigarettes citing an epidemic of use among teens. http://www.bbc.com//news/business-455008942018-09-13
These engineered organs are going through clinical trials for approval by the US Food and Drug Administration NegativeBioprinting human tissue using specialised 3D printers promises to transform medicine with implications for organ transplants cancer treatment and antibiotic development http://www.bbc.com//news/business-454707992018-09-11
The company began its investigation with the thirdparty manufacturer that produces Honey Smacks immediately after being contacted by the US Food Drug Administration and Centers for Disease Control Kelloggs said NegativeKellogg Company is voluntarily recalling 1 http://www.bbc.com//news/business-444919022018-06-15
Patients were able to apply to the US Food and Drug Administration for access to nonapproved drugs before and most were granted permission. NegativePresident Donald Trump has signed a bill giving terminally ill patients the right to try experimental treatments not approved by the government. http://www.bbc.com//news/world-us-canada-443059982018-05-30
But in conversation with the BBC he described it as a treatment a claim that had the potential to attract the attention of the US Food and Drug Administration. PositiveA biohacker who became infamous after apparently injecting himself with an untested herpes drug in front of an audience has been found dead http://www.bbc.com//news/technology-439735882018-05-02
The US Food and Drug Administration has warned against eating raw dough batter or cake mixture because of the risk of E coli from flour NegativeThe US Food and Drug Administration has warned against eating raw dough batter or cake mixture because of the risk of E. coli from flourhttp://www.bbc.com//news/health-422367022017-12-08










This query took 8.1774718761444 seconds.