The new data will be displayed in a poster presentation on Monday, December 7, from 2:30 to 5:00 pm PST (board 3-157). The study, entitled “A Randomized, Double-Blind, Placebo-Controlled, Single Dose, Crossover Study of the Pharmacokinetics, Safety and Tolerability of Ibuprofen Injection in Healthy Adult Volunteers,” will be presented by the principal author, Leo Pavliv, RPh, MBA.
Concurrent with the presentation, copies of the poster will be available on Cumberland Pharmaceuticals’ website at http://investor.shareholder.com/cpix/events.cfm or by contacting the Company at 615-255-0068.
SOURCE: Cumberland Pharmaceuticals Inc.
Caldolor is indicated for the management of mild to moderate pain and management of moderate to severe pain as an adjunct to opioid analgesics, and for the reduction of fever in adults. It is the first FDA approved intravenous therapy for fever. Caldolor is contraindicated in patients with known hypersensitivity to ibuprofen or other NSAIDs, patients with asthma, urticaria, or allergic type reactions after taking aspirin or other NSAIDs. Caldolor is contraindicated for use during the peri-operative period in the setting of coronary artery bypass graft (CABG) surgery. Caldolor should be used with caution in patients with prior history of ulcer disease or GI bleeding, in patients with fluid retention or heart failure, in the elderly, those with renal impairment, heart failure, liver impairment, and those taking diuretics or ACE inhibitors. Blood pressure should be monitored during treatment with Caldolor. For full prescribing information, including boxed warning, visit www.caldolor.com.
CONTACT: Investors, Angela Novak of Cumberland Pharmaceuticals,
+1-615-255-0068, investors@cumberlandpharma.com; or Media, Paula Lovell of
Lovell Communications, +1-615-972-2964, lovell@lovell.com, for Cumberland
Pharmaceuticals Inc.
Web site: http://www.ashp.org/
http://www.caldolor.com/
http://www.cumberlandpharma.com/