Recommended Pages at empr.com
Latuda Dosing Range Updated - MPR
empr.com — “Sunovion announced that the FDA has approved an expanded dose range for Latuda (lurasidone) tablets in the treatment of adult patients with schizophrenia.” View full resource at empr.com
Most Recently Shared on May 7, 2012 at 6:52 pm By:
Latuda Dosing Range Updated #sunovion #antipsychotic #schizophrenia http://t.co/Bkpd52pO
Phase 3 Study of Aripiprazole Intramuscular Depot for the Maintenance Treatment of Schizophrenia - MPR
empr.com — “Otsuka and Lundbeck announced results from a Phase 3 clinical trial evaluating the efficacy, safety and tolerability of once-monthly aripiprazole intramuscular (IM) depot formulation for the maintenance treatment of adults with schizophrenia.” View full resource at empr.com
Most Recently Shared on May 7, 2012 at 5:18 pm By:
Phase 3 Study of #Aripiprazole Intramuscular Depot for the Maintenance Treatment of #Schizophrenia http://t.co/hAN0om32
FDA Issues Complete Response Letter to NDA for Adasuve - MPR
empr.com — “Alexza Pharmaceuticals announced that it has received a complete response letter from the FDA regarding its New Drug Application (NDA) for Adasuve (Staccato loxapine) inhalation powder, 5mg and 10mg, for the acute treatment of agitation associated with schizophrenia or bipolar I disorder in adults.” View full resource at empr.com
Most Recently Shared on May 7, 2012 at 3:35 pm By:
FDA Issues Complete Response Letter to NDA for #Adasuve #Alexza #loxapine #inhalation #agitation http://t.co/UloQRAV8
Phase 3 Trial Update of Latuda for Bipolar I Depression - MPR
empr.com — “Dainippon Sumitomo Pharma announced results from two Phase 3 clinical trials designed to evaluate the efficacy and safety of Latuda (lurasidone; Sunovion) as adjunctive therapy and monotherapy, respectively, in patients with bipolar I depression (PREVAIL 1 and PREVAIL 2; PRogram to EValuate the Antidepressant Impact of Lurasidone).” View full resource at empr.com
Most Recently Shared on May 7, 2012 at 2:27 pm By:
Phase 3 Trial Update of #Latuda for #Bipolar I #Depression http://t.co/qSy2y0ba
RECALL: Franck's Compounding Triamcinolone Acetonide Recall - MPR
empr.com — “Franck's Compounding Pharmacy has recalled one additional lot of triamcinolone acetonide PF 80mg/mL.” View full resource at empr.com
Most Recently Shared on May 4, 2012 at 7:31 pm By:
#RECALL: Franck's Compounding Triamcinolone Acetonide Recall #ophthalmologist #infection http://t.co/PkKV2YhX
Phase 3 Study Update of 4-Factor Prothrombin Complex Concentrate for Hemostasis - MPR
empr.com — “CSL Behring announced results of a Phase 3b study that showed that a balanced, human 4-factor prothrombin complex concentrate (PCC) is as effective as the current standard of treatment in stopping bleeding in patients receiving vitamin K antagonist therapy (eg, warfarin).” View full resource at empr.com
Most Recently Shared on May 4, 2012 at 6:07 pm By:
Phase 3 Study Update of 4-Factor #Prothrombin Complex Concentrate for #Hemostasis #hematology #bleeding http://t.co/v674R0I1
Phase 3 Study Update of Gattex for Adult Short Bowel Syndrome - MPR
empr.com — “NPS Pharmaceuticals reported that four additional patients have successfully achieved independence from parenteral nutrition (PN) and intravenous (IV) fluids while on long-term Gattex (teduglutide) therapy in STEPS 2, a 24-month open-label study in adult short bowel syndrome (SBS).” View full resource at empr.com
Most Recently Shared on May 3, 2012 at 1:42 pm By:
Phase 3 Study Update of #Gattex for Adult Short Bowel Syndrome #gastrointestinal #teduglutide http://t.co/iSRCodf7
Dymista Approved for Allergic Rhinitis - MPR
empr.com — “Meda announced that the FDA has approved Dymista (azelastine HCl and fluticasone propionate) nasal spray for the treatment of seasonal allergic rhinitis.” View full resource at empr.com
Most Recently Shared on May 2, 2012 at 2:02 pm By:
Dymista Approved for #Allergic Rhinitis #meda #nasal http://t.co/kCeKMvUM
QNASL - New Product Releases - MPR
empr.com — “Seasonal and perennial allergic rhinitis.” View full resource at empr.com
Most Recently Shared on May 2, 2012 at 1:06 pm By:
NEW PRODUCT: Learn more about QNASL for seasonal and perennial allergic rhinitis http://t.co/oo0KDmhl #allergies
Phase 3 Study Update of Quadrivalent Influenza Vaccine in Pediatric Population - MPR
empr.com — “Sanofi Pasteur, the vaccines division of Sanofi Aventis, announced new Phase 3 data for its investigational quadrivalent influenza vaccine (QIV) in children.” View full resource at empr.com
Most Recently Shared on May 1, 2012 at 6:57 pm By:
Phase 3 Study Update of Quadrivalent #Influenza #Vaccine in #Pediatric Population #Sanofi #pediatrician #immunization http://t.co/XI20ORHX
Mylan Launches Generic Doryx 150mg - MPR
empr.com — “Mylan announced the launch of Doxycycline hyclate delayed-release (DR) tablets, 150mg, the generic version of Warner Chilcott's Doryx tablets.” View full resource at empr.com
Most Recently Shared on May 1, 2012 at 2:35 pm By:
#Mylan Launches #Generic Doryx 150mg #antibiotic #acne http://t.co/jzTB1KKP
AAN: Migraine Prevalence Up in Celiac Disease, IBD Patients - MPR
empr.com — “Patients with celiac disease or inflammatory bowel disease (IBD) and those self-classified with gluten sensitivity (GS) have increased prevalence of migraine.” View full resource at empr.com
Most Recently Shared on April 30, 2012 at 11:07 pm By:
AAN: Migraine Prevalence Up in Celiac Disease, IBD Patients - MPR http://t.co/xoavZaPe
Voraxaze Injection Now Available - MPR
empr.com — “Voraxaze Injection Now Available - MPR” View full resource at empr.com
Most Recently Shared on April 30, 2012 at 3:06 pm By:
Voraxaze Injection Now Available #BTG #methotrexate #oncology http://t.co/8qMcfs5E
Stendra Approved for Erectile Dysfunction - MPR
empr.com — “The FDA announced that it has approved Stendra (avanafil; Vivus Inc.) tablets for the treatment of erectile dysfunction.” View full resource at empr.com
Most Recently Shared on April 30, 2012 at 1:54 pm By:
Stendra Approved for Erectile Dysfunction #urologist #pharmacist #ED http://t.co/V6vwnKR7
FDA Issues Complete Response Letter to sBLA for Xgeva - MPR
empr.com — “Amgen announced that it received a complete response letter from the FDA for it supplemental Biologics License Application (sBLA) for Xgeva (denosumab) injection for the treatment of men with castration-resistant prostate cancer (CRPC) at high risk of developing bone metastases.” View full resource at empr.com
Most Recently Shared on April 27, 2012 at 4:02 pm By:
FDA Issues Complete Response Letter to sBLA for Xgeva #amgen #prostate #oncology http://t.co/9fR1ub9L

