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Stock Market & Financial Investment News

News Breaks
April 2, 2014
06:25 EDTHSP, MDCOThe Medicines Co. downgraded to Neutral from Overweight at Piper Jaffray
Piper Jaffray downgraded The Medicines Co. (MDCO) to Neutral after a court ruled the company failed to prove its patents were infringed by Hospira (HSP).
News For MDCO;HSP From The Last 14 Days
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October 22, 2014
09:45 EDTMDCOThe Medicines Co. says 'as open as can possibly be' to potential takeover
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09:21 EDTMDCOThe Medicines Co. lowers 2014 revenue outlook to $720M-$735M
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07:21 EDTHSPU.S. DHS investigates medical gear for potential cyber defects, Reuters says
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07:11 EDTMDCOMedicines Co. says Angiomax, Angiox revenue up 5% in first nine months
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07:06 EDTMDCOThe Medicines Co. reports Q3 EPS (26c) , consensus (12c)
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October 20, 2014
09:48 EDTMDCOBrdiger Management reports 5.1% passive stake in The Medicines Co.
08:04 EDTHSPGerman fund pressured to sell Mylan stake over drug used in executions, FT says
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October 19, 2014
14:18 EDTHSPFresenius, others explore bid for Danone medical nutrition unit, Reuters says
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October 14, 2014
11:23 EDTHSPBIND Therapeutics and The Conference Forum hold a conference
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October 13, 2014
07:25 EDTMDCOEuropean Association of Cardiothoracic Surgery to hold annual meeting
28th EACTS Annual Meeting is being held in Milan, Italy on October 11-15.
October 10, 2014
07:14 EDTMDCOThe Medicines Co's Q3 Angiomax estimate lowered at Credit Suisse
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October 9, 2014
16:57 EDTMDCOThe Medicines Co. announces journal publication of SOLO II phase 3 trial
The Medicines Company announced the publication of the results from the SOLO II phase 3 clinical trial of ORBACTIV, or oritavancin, for injection in the journal Clinical Infectious Diseases. ORBACTIV, is the first and only single dose intravenous antibiotic approved by FDA for the treatment of adults with Acute Bacterial Skin and Skin Structure Infections, or ABSSSI, caused or suspected to be caused by susceptible isolates of designated Gram-positive pathogens. The publication reported that a single, once only, 1200 mg intravenous dose of ORBACTIVTM was non-inferior to twice-daily intravenous dosing of vancomycin given for 7 to 10 days in patients with ABSSSI caused or suspected to be caused by Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus. A single 1200 mg IV dose of ORBACTIV results in efficacy in ABSSSIs that is comparable and statistically non-inferior to vancomycin administered intravenously for 7-10 days. ORBACTIV had a safety profile comparable to vancomycin when monitored for up to 60 days following a single dose, with similar intensity, onset and duration of AEs.
October 8, 2014
13:00 EDTHSPHospira recalling one lot of Vancomycin Hydrochloride
The FDA announced that Hospira is initiating a voluntary nationwide user-level recall of one lot of Vancomycin Hydrochloride. The action is because the product may have experienced temperature excursions during shipment to a customer and then was further distributed by the customer, the agency said. It added that there have been no adverse events or complaints reported for the affected lot. Hospira is "undertaking the recall out of an abundance of caution," the FDA said.

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