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Stock Market & Financial Investment News

News Breaks
April 29, 2013
12:55 EDTPFEEarnings Preview: Pfizer shares up about 12% since reporting Q4 results
Pfizer (PFE) is scheduled to report Q1 earnings before the open on Tuesday, April 30, with a conference call scheduled for 10:00 am ET. Pfizer develops and produces medicines and vaccines for a wide range of conditions including in the areas of immunology and inflammation, oncology, cardiovascular and metabolic diseases, neuroscience and pain. EXPECTATIONS: Analysts are looking for EPS of 56c on revenue of $14.0B, according to First Call. The consensus range for EPS is 52c-63c on revenue of $13.06B-$14.37B. LAST QUARTER: Pfizer reported Q4 EPS of 47c against estimates of 44c on revenue of $15.1B against estimates of $14.37B. Pfizer cited Lipitor's loss of exclusivity in most major markets as a negative in Q4. At the time of its Q4 earnings release, the drug giant gave FY13 EPS guidance of $2.20-$2.30 on a consensus of $2.29. STREET RESEARCH: On March 18, Wells Fargo called Pfizer its top large cap pick in Pharma. PRICE ACTION: Pfizer shares are up approximately 12% since reporting Q4 results on January 29.
News For PFE From The Last 14 Days
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March 2, 2015
16:31 EDTPFEPfizer files automatic mixed securities shelf
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09:02 EDTPFEAstraZeneca mulls linking bonuses to Pfizer defense pledges, Sunday Times says
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February 26, 2015
12:31 EDTPFEPfizer says CDC recommends serogroup B meningococcal vaccine for those at risk
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February 24, 2015
08:07 EDTPFEPfizer announces Trumenba studies met primary objectives
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February 20, 2015
10:33 EDTPFEBattleground update: AbbVie named top global pick at Jefferies
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10:31 EDTPFEPfizer announces FDA acceptance of NDA for Rapamune
Pfizer announced that the FDA has accepted for priority review a supplemental New Drug Application for RAPAMUNE for the treatment of lymphangioleiomyomatosis, a rare, progressive lung disease in women of childbearing age that is often fatal. With the Priority Review designation for the sNDA, Pfizer anticipates a decision in June of 2015 based on the anticipated Prescription Drug User Fee Act action date. The sNDA is based on results from the Multicenter International Lymphangioleiomyomatosis Efficacy and Safety of Sirolimus Trial. The MILES Trial included 89 LAM patients with moderate lung impairment who were randomized to receive RAPAMUNE or placebo for 12 months, followed by a 12 month observation period. In the trial, those treated with RAPAMUNE for one year experienced stabilization of lung function as measured by forced expiratory volume in one second.
07:23 EDTPFEAbbVie replaces Pfizer as top global pharma pick at Jefferies
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February 19, 2015
18:25 EDTPFEPiper Jaffray biotech analyst to hold analyst/industry conference call
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14:49 EDTPFEWalgreens selected by Pfizer as one of pharmacies to dispense Ibrance
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07:12 EDTPFEWharton Health Care Club to hold a conference
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February 17, 2015
15:36 EDTPFETianyin JCM plans for FDA certification process
Tianyin Pharmaceutical (TPI) updated on the business and development at its Jiangchuan Macrolide Facility, or JCM, active pharmaceutical ingredients operation. In addition to JCM's certification at India, along with other international clients located at Bangladesh, Philippines and Iran on import status, TPI plans for FDA certification process at its JCM facility in order to service international clients such as Pfizer's (PFE) and their subsidiaries in China, the company said. "This is expected to translate to further demand for JCM's macrolide API business in both the domestic and international markets," Tianyin stated.
10:01 EDTPFECVS says PCSK9 inhibitors could cost system $150B annually
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