dizziness Press Release

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Mon, 05/03/2021 - 06:47 Top news stories from AMA Morning Rounds: Week of May 3, 2021
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AMA
Wed, 01/08/2020 - 21:11 Blueprint Medicines Announces FDA Approval of AYVAKIT (avapritinib) for the Treatment of Adults with Unresectable or Metastatic PDGFRA Exon 18 Mutant Gastrointestinal Stromal Tumor
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Blueprint Medicines
Tue, 03/05/2019 - 08:40 SPRAVATO uses the first new mechanism of action in decades to treat major depressive disorder 1,2,3
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Johnson and Johnson
Wed, 01/30/2019 - 03:32 SUPPLEMENTARY NEW DRUG APPLICATION SUBMITTED IN JAPAN FOR FYCOMPA AS MONOTHERAPY FOR PARTIAL-ONSET SEIZURES, PEDIATRIC INDICATION FOR PARTIAL-ONSET SEIZURES, AS WELL AS NEW FORMULATION
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EISAI
Fri, 12/21/2018 - 16:11 Acorda Therapeutics Announces FDA Approval of INBRIJA (levodopa inhalation powder)
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Acorda
Thu, 12/20/2018 - 03:42 LYNPARZA (olaparib) Meets Primary Endpoint in Phase 3 SOLO-3 Trial for the Treatment of Relapsed BRCA-Mutated Advanced Ovarian Cancer
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Cubist Pharmace...
Wed, 12/19/2018 - 04:35 LYNPARZA (olaparib) Approved by FDA for First-Line Maintenance Therapy in BRCA-Mutated Advanced Ovarian Cancer
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Cubist Pharmace...
Sun, 12/16/2018 - 23:00 Patient-centered Care is the Focus and Priority of the 2019 Standards of Medical Care in Diabetes, Published Today by the American Diabetes Association
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American Diabet...
Wed, 12/12/2018 - 10:47 Havana Embassy Phenomenon: Researchers Report Acute Findings
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UniversityofPit...
Mon, 12/10/2018 - 07:06 Astellas Launches XOSPATA (gilteritinib) in the U.S. for the Treatment of Adult Patients with Relapsed/Refractory Acute Myeloid Leukemia (AML) with a FLT3 Mutation
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Astellas
Fri, 12/07/2018 - 02:26 Opioid Prescriptions Can Be Drastically Reduced After Surgery with No Increase in Pain, Study Shows
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Roswell Park Ca...
Wed, 12/05/2018 - 21:55 FDA Approves Genentechs Tecentriq in Combination With Avastin and Chemotherapy for the Initial Treatment of People With a Specific Type of Metastatic Lung Cancer
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Genentech
Tue, 12/04/2018 - 23:19 Genentechs Kadcyla Cut the Risk of Disease Recurring by Half Compared to Herceptin in People With HER2-Positive Early Breast Cancer With Residual Disease After Neoadjuvant Treatment
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Genentech
Mon, 12/03/2018 - 20:55 FDA Grants Priority Review to Genentechs Tecentriq in Combination With Chemotherapy for the Initial Treatment of Extensive-Stage Small Cell Lung Cancer
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Genentech
Mon, 12/03/2018 - 06:01 Astellas Presents Updated Results from Phase 1 Study of Gilteritinib Plus Chemotherapy in Patients with Newly Diagnosed Acute Myeloid Leukemia (AML)
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Astellas
Sun, 12/02/2018 - 23:09 New Venclexta Data Demonstrate Deep Responses in Two of the Most Common Types of Leukemia
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Genentech
Sun, 12/02/2018 - 10:54 Celgene Corporation Announces Results of AUGMENT Evaluating REVLIMID In Combination with Rituximab (R) In Patients with Relapsed/Refractory Indolent Lymphoma At ASH 2018
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BMS
Sat, 12/01/2018 - 23:31 Real-world data show Novartis drug Revolade improves outcomes for ITP patients compared to other second-line therapies
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Novartis
Sat, 12/01/2018 - 05:02 Regeneron Presents Positive Data at ASH for REGN1979 CD20xCD3 Bispecific Antibody in Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma
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Regeneron
Sat, 12/01/2018 - 01:20 Novartis announces longer-term analyses from pivotal Kymriah trials that showed durable responses are maintained in patients with advanced blood cancers
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Novartis
Wed, 11/28/2018 - 17:56 Approvals Based on Findings from the Pivotal Phase 3 DRIVE-AHEAD and DRIVE-FORWARD Trials Evaluating the Efficacy and Safety of DELSTRIGO and PIFELTRO Through 96 Weeks
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Merck
Wed, 11/28/2018 - 05:50 XOSPATA (gilteritinib) Approved by U.S. FDA for Adult Patients with Relapsed/Refractory Acute Myeloid Leukemia (AML) with a FLT3 Mutation
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Astellas
Tue, 11/27/2018 - 12:13 Tevas Generic Version of EpiPen (Epinephrine Injection, USP) Auto-Injector 0.3 mg Now Available in Limited Quantity in the United States
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Teva Pharmaceutical
Tue, 11/27/2018 - 07:08 Tevas Generic Epinephrine Injection Now Available in Limited Quantity in the US
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Teva Pharmaceutical
Mon, 11/26/2018 - 20:32 Pfizer Receives Six Months Pediatric Exclusivity for LYRICA (pregabalin)
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Pfizer