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     <channel> <title>Medical News</title>
      <link>http://www.drugsfreelist.com/medical_media_news</link>
      <description>Medical News</description>
      <language>Enghlish</language>
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<title>U.S. Food And Drug Administration Approves Pfizer’s INLYTA (axitinib) For Patients With Previously Treated Advanced Renal Cell Carcinoma (RCC)</title>
<link>http://www.drugsfreelist.com/medical_media_news/6384/U_S__Food_And_Drug_Administration_Approves_Pfizer’s_INLYTA__axitinib__For_Patients_With_Previously_Treated_Advanced_Renal_Cell_Carcinoma__RCC_</link>
<description><![CDATA[-Pfizer Inc. announced  that the U.S. Food and Drug Administration (FDA) has approved INLYTA® (axitinib), a kinase inhibitor, for the treatment of patients with advanced renal cell carcinoma (RCC)]]></description>
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<title>Pfizer Announces FDA Acceptance Of New Drug Application For Bosutinib For Patients With Previously Treated Ph Chronic Myeloid Leukemia</title>
<link>http://www.drugsfreelist.com/medical_media_news/6383/Pfizer_Announces_FDA_Acceptance_Of_New_Drug_Application_For_Bosutinib_For_Patients_With_Previously_Treated_Ph_Chronic_Myeloid_Leukemia</link>
<description><![CDATA[Pfizer Inc. announced  that the U.S. Food and Drug Administration (FDA) has accepted its New Drug Application (NDA) for standard review of bosutinib as a treatment option for adult patients with previously treated Philadelphia chromosome positive (Ph+) chronic myeloid leukemia (CML).]]></description>
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<title> FDA approves Inlyta to treat patients with a type of advanced kidney cancer</title>
<link>http://www.drugsfreelist.com/medical_media_news/6382/_FDA_approves_Inlyta_to_treat_patients_with_a_type_of_advanced_kidney_cancer</link>
<description><![CDATA[The U.S. Food and Drug Administration  approved Inlyta (axitinib) to treat patients with advanced kidney cancer (renal cell carcinoma) who have not responded to another drug for this type of cancer.]]></description>
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<title>FDA Drug Safety Communication: New risk factor for Progressive Multifocal Leukoencephalopathy (PML) associated with Tysabri (natalizumab)</title>
<link>http://www.drugsfreelist.com/medical_media_news/6381/FDA_Drug_Safety_Communication:_New_risk_factor_for_Progressive_Multifocal_Leukoencephalopathy__PML__associated_with_Tysabri__natalizumab_</link>
<description><![CDATA[The U.S. Food and Drug Administration (FDA) is informing the public that testing positive for anti-JC virus (JCV) antibodies has been identified as a risk factor for progressive multifocal leukoencephalopathy (PML).]]></description>
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<title>FDA. New and Generic Drug Approvals - January 27, 2012</title>
<link>http://www.drugsfreelist.com/medical_media_news/6380/FDA__New_and_Generic_Drug_Approvals_-_January_27,_2012</link>
<description><![CDATA[New drugs approved. List of drugs approved by FDA to date January 27, 2012 ]]></description>
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<title>FDA. New and Generic Drug Approvals - January 26, 2012</title>
<link>http://www.drugsfreelist.com/medical_media_news/6379/FDA__New_and_Generic_Drug_Approvals_-_January_26,_2012</link>
<description><![CDATA[New drugs approved. List of drugs approved by FDA to date January 26, 2012 ]]></description>
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<title>FDA. New and Generic Drug Approvals - January 25, 2012</title>
<link>http://www.drugsfreelist.com/medical_media_news/6378/FDA__New_and_Generic_Drug_Approvals_-_January_25,_2012</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date January 25, 2012 ]]></description>
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<title>FDA. New and Generic Drug Approvals - January 24, 2012</title>
<link>http://www.drugsfreelist.com/medical_media_news/6377/FDA__New_and_Generic_Drug_Approvals_-_January_24,_2012</link>
<description><![CDATA[New drugs approved. List of drugs approved by FDA to date January 24, 2012 ]]></description>
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<title>FDA. New and Generic Drug Approvals - January 23, 2012</title>
<link>http://www.drugsfreelist.com/medical_media_news/6376/FDA__New_and_Generic_Drug_Approvals_-_January_23,_2012</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date January 23, 2012 ]]></description>
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<title>FDA. New and Generic Drug Approvals - January 20, 2012</title>
<link>http://www.drugsfreelist.com/medical_media_news/6375/FDA__New_and_Generic_Drug_Approvals_-_January_20,_2012</link>
<description><![CDATA[New drugs approved. List of drugs approved by FDA to date January 20, 2012 ]]></description>
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<title>FDA. New and Generic Drug Approvals - January 19, 2012</title>
<link>http://www.drugsfreelist.com/medical_media_news/6374/FDA__New_and_Generic_Drug_Approvals_-_January_19,_2012</link>
<description><![CDATA[New drugs approved. List of drugs approved by FDA to date January 19, 2012 ]]></description>
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<title>FDA. New and Generic Drug Approvals - January 18, 2012</title>
<link>http://www.drugsfreelist.com/medical_media_news/6373/FDA__New_and_Generic_Drug_Approvals_-_January_18,_2012</link>
<description><![CDATA[New drugs approved. List of drugs approved by FDA to date January 18, 2012 ]]></description>
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<title>FDA expands use of endovascular graft to treat aortic tears</title>
<link>http://www.drugsfreelist.com/medical_media_news/6372/FDA_expands_use_of_endovascular_graft_to_treat_aortic_tears</link>
<description><![CDATA[The U.S. Food and Drug Administration  expanded the approved usage for an endovascular graft manufactured by W.L. Gore and Associates Inc. to include treatment of life-threatening tears or ruptures of the aorta (thoracic aortic transection).]]></description>
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<title>FDA approves Voraxaze to treat patients with toxic methotrexate levels </title>
<link>http://www.drugsfreelist.com/medical_media_news/6371/FDA_approves_Voraxaze_to_treat_patients_with_toxic_methotrexate_levels_</link>
<description><![CDATA[The U.S. Food and Drug Administration approved Voraxaze (glucarpidase) to treat patients with toxic levels of methotrexate in their blood due to kidney failure.]]></description>
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<title>FDA Drug Safety Communication: New Boxed Warning and Contraindication for Adcetris (brentuximab vedotin)</title>
<link>http://www.drugsfreelist.com/medical_media_news/6370/FDA_Drug_Safety_Communication:_New_Boxed_Warning_and_Contraindication_for_Adcetris__brentuximab_vedotin_</link>
<description><![CDATA[The U.S. Food and Drug Administration (FDA) is notifying the public that two additional cases of progressive multifocal leukoencephalopathy (PML), a rare but serious brain infection that can result in death, have been reported with the lymphoma drug Adcetris (brentuximab vedotin).]]></description>
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<title>FDA Drug Safety Communication: Update: Preliminary findings from ongoing investigations of CardioGen-82</title>
<link>http://www.drugsfreelist.com/medical_media_news/6369/FDA_Drug_Safety_Communication:_Update:_Preliminary_findings_from_ongoing_investigations_of_CardioGen-82</link>
<description><![CDATA[The U.S. Food and Drug Administration (FDA) is updating healthcare professionals and the public about preliminary findings from ongoing investigations following the voluntary recall of CardioGen-82 on July 25, 2011]]></description>
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<title>FDA. New and Generic Drug Approvals - January 12, 2012</title>
<link>http://www.drugsfreelist.com/medical_media_news/6368/FDA__New_and_Generic_Drug_Approvals_-_January_12,_2012</link>
<description><![CDATA[New drugs approved. List of drugs approved by FDA to date January 12, 2012]]></description>
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<title>FDA. New and Generic Drug Approvals - January 17, 2012</title>
<link>http://www.drugsfreelist.com/medical_media_news/6367/FDA__New_and_Generic_Drug_Approvals_-_January_17,_2012</link>
<description><![CDATA[New drugs approved .List of drugs approved by FDA to date January 17, 2012]]></description>
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<title>FDA. New and Generic Drug Approvals - January 13, 2012</title>
<link>http://www.drugsfreelist.com/medical_media_news/6366/FDA__New_and_Generic_Drug_Approvals_-_January_13,_2012</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date January 13, 2012]]></description>
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<title>FDA Approves Merck’s ISENTRESS (raltegravir) for Use in Children Ages Two Years and Older as Part of HIV-1 Combination Therapy</title>
<link>http://www.drugsfreelist.com/medical_media_news/6365/FDA_Approves_Merck’s_ISENTRESS__raltegravir__for_Use_in_Children_Ages_Two_Years_and_Older_as_Part_of_HIV-1_Combination_Therapy</link>
<description><![CDATA[Merck, known as MSD outside the United States and Canada, announced  that the U.S. Food and Drug Administration (FDA) recently approved the use of ISENTRESS® (raltegravir) in combination with other antiretroviral (ARV) medicines, for the treatment of HIV-1 infection in pediatric patients two years of age and older and weighing at least 10 kg. ]]></description>
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<title>GSK and Theravance announce initial outcomes from pivotal Phase III studies for once-daily Relovair  in COPD and asthma</title>
<link>http://www.drugsfreelist.com/medical_media_news/6364/GSK_and_Theravance_announce_initial_outcomes_from_pivotal_Phase_III_studies_for_once-daily_Relovair__in_COPD_and_asthma</link>
<description><![CDATA[GlaxoSmithKline and Theravance, Inc. announced the completion of the phase III registration programme for the once-daily investigational medicine Relovair]]></description>
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<title>Biogen Idec and Isis Pharmaceuticals Announce Global Collaboration for Antisense Program Targeting Spinal Muscular Atrophy</title>
<link>http://www.drugsfreelist.com/medical_media_news/6363/Biogen_Idec_and_Isis_Pharmaceuticals_Announce_Global_Collaboration_for_Antisense_Program_Targeting_Spinal_Muscular_Atrophy</link>
<description><![CDATA[Biogen Idec  and Isis Pharmaceuticals, Inc. announced that they have entered into an exclusive, worldwide option and collaboration agreement under which the companies will develop and commercialize Isis’ antisense investigational drug, ISIS-SMNRx, for the treatment of spinal muscular atrophy (SMA).]]></description>
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<title>Shire Acquires US Rights to Resolor</title>
<link>http://www.drugsfreelist.com/medical_media_news/6362/Shire_Acquires_US_Rights_to_Resolor</link>
<description><![CDATA[Shire, the global specialty biopharmaceutical company, announced that it has acquired the rights to develop and market Resolor® (prucalopride) in the United States (US) in an agreement  with Janssen Pharmaceutica N.V. ]]></description>
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<title>Shire’s VENVANSE® (lisdexamfetamine dimesylate) Marketing Application accepted for review in Europe</title>
<link>http://www.drugsfreelist.com/medical_media_news/6361/Shire’s_VENVANSE®__lisdexamfetamine_dimesylate__Marketing_Application_accepted_for_review_in_Europe</link>
<description><![CDATA[Shire plc, the global specialty biopharmaceutical company,  announced the acceptance for review of their once-daily ADHD medicinal product VENVANSE® (lisdexamfetamine dimesylate) by the Medicines Healthcare products Regulatory Agency (MHRA), UK. ]]></description>
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<title>Mylan Confirms First-to-File Patent Challenge Relating to Actoplus Met XR Tablets</title>
<link>http://www.drugsfreelist.com/medical_media_news/6360/Mylan_Confirms_First-to-File_Patent_Challenge_Relating_to_Actoplus_Met_XR_Tablets</link>
<description><![CDATA[Mylan confirmed that the company has been sued by Takeda Pharmaceutical Company, Watson Pharmaceuticals and Andrx Labs in connection with the filing of an Abbreviated New Drug Application (ANDA) with the U.S. Food and Drug Administration (FDA) for Pioglitazone Hydrochloride and Extended-release Metformin Hydrochloride tablets, 15 mg/1000 mg and 30 mg/1000 mg.]]></description>
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<title>Mylan Launches First Generic Version of Teveten Tablets</title>
<link>http://www.drugsfreelist.com/medical_media_news/6359/Mylan_Launches_First_Generic_Version_of_Teveten_Tablets</link>
<description><![CDATA[Mylan announced that its subsidiary Mylan Pharmaceuticals Inc. has received final approval from the U.S. Food and Drug Administration for its Abbreviated New Drug Application for Eprosartan Mesylate Tablets, 400 mg (base) and 600 mg (base). ]]></description>
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<title>FDA to protect important class of antimicrobial drugs for treating human illness</title>
<link>http://www.drugsfreelist.com/medical_media_news/6358/FDA_to_protect_important_class_of_antimicrobial_drugs_for_treating_human_illness</link>
<description><![CDATA[The U.S. Food and Drug Administration  issued an order that prohibits certain uses of the cephalosporin class of antimicrobial drugs in cattle, swine, chickens and turkeys effective April 5, 2012.
 ]]></description>
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<title>Genzyme Reports Top-line Results for TENERE Study of Oral Teriflunomide in Relapsing Multiple Sclerosis</title>
<link>http://www.drugsfreelist.com/medical_media_news/6357/Genzyme_Reports_Top-line_Results_for_TENERE_Study_of_Oral_Teriflunomide_in_Relapsing_Multiple_Sclerosis</link>
<description><![CDATA[Genzyme, a Sanofi company,  reported top-line results from TENERE, a Phase III clinical trial comparing the effectiveness, safety and tolerability of once-daily oral teriflunomide to interferon beta-1a (Rebif®), an approved injectable therapy, in people with relapsing forms of multiple sclerosis (RMS).]]></description>
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<title>Boston Scientific Receives FDA Approval for New Infinion™ 16 Percutaneous Lead for Precision Plus Spinal Cord Stimulator System</title>
<link>http://www.drugsfreelist.com/medical_media_news/6356/Boston_Scientific_Receives_FDA_Approval_for_New_Infinion™_16_Percutaneous_Lead_for_Precision_Plus_Spinal_Cord_Stimulator_System</link>
<description><![CDATA[Boston Scientific Corporation (NYSE: BSX) announces U.S. Food and Drug Administration (FDA) approval of the Infinion™ 16 Percutaneous Lead for its Precision Plus™ Spinal Cord Stimulator (SCS) System, the first rechargeable SCS device for chronic pain management.]]></description>
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<title>FDA Approves Baxter`s ADVATE as the Only FVIII for Routine Prophylaxis in Both Adults and Children with Hemophilia A</title>
<link>http://www.drugsfreelist.com/medical_media_news/6355/FDA_Approves_Baxter`s_ADVATE_as_the_Only_FVIII_for_Routine_Prophylaxis_in_Both_Adults_and_Children_with_Hemophilia_A</link>
<description><![CDATA[Baxter International Inc.  announced that the U.S. Food and Drug Administration (FDA) has approved ADVATE [Antihemophilic Factor (Recombinant) Plasma/Albumin Free Method] for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in patients with hemophilia A. ]]></description>
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<title>FDA approves mechanical cardiac assist device for children with heart failure</title>
<link>http://www.drugsfreelist.com/medical_media_news/6354/FDA_approves_mechanical_cardiac_assist_device_for_children_with_heart_failure</link>
<description><![CDATA[The U.S. Food and Drug Administration  approved a medical device that supports the weakened heart of children with heart failure to help keep them alive until a donor for a heart transplant can be found.]]></description>
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<title>FDA Drug Safety Communication: Selective serotonin reuptake inhibitor (SSRI) antidepressant use during pregnancy and reports of a rare heart and lung condition in newborn babies</title>
<link>http://www.drugsfreelist.com/medical_media_news/6353/FDA_Drug_Safety_Communication:_Selective_serotonin_reuptake_inhibitor__SSRI__antidepressant_use_during_pregnancy_and_reports_of_a_rare_heart_and_lung_condition_in_newborn_babies</link>
<description><![CDATA[The U.S. Food and Drug Administration (FDA) is updating the public on the use of selective serotonin reuptake inhibitor (SSRI) antidepressants by women during pregnancy and the potential risk of a rare heart and lung condition known as persistent pulmonary hypertension of the newborn (PPHN). ]]></description>
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<title>FDA. New and Generic Drug Approvals - December 20, 2011</title>
<link>http://www.drugsfreelist.com/medical_media_news/6352/FDA__New_and_Generic_Drug_Approvals_-_December_20,_2011</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date December 20, 2011 ]]></description>
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<title>FDA. New and Generic Drug Approvals - December 16, 2011</title>
<link>http://www.drugsfreelist.com/medical_media_news/6351/FDA__New_and_Generic_Drug_Approvals_-_December_16,_2011</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date December 16, 2011 ]]></description>
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<title>FDA. New and Generic Drug Approvals - December 15, 2011</title>
<link>http://www.drugsfreelist.com/medical_media_news/6350/FDA__New_and_Generic_Drug_Approvals_-_December_15,_2011</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date December 15, 2011 ]]></description>
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<title>FDA. New and Generic Drug Approvals - December 14, 2011</title>
<link>http://www.drugsfreelist.com/medical_media_news/6349/FDA__New_and_Generic_Drug_Approvals_-_December_14,_2011</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date December 14, 2011 ]]></description>
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<title>FDA permits marketing of the first hand-held device to aid in the detection of bleeding in the skull</title>
<link>http://www.drugsfreelist.com/medical_media_news/6348/FDA_permits_marketing_of_the_first_hand-held_device_to_aid_in_the_detection_of_bleeding_in_the_skull</link>
<description><![CDATA[The U.S. Food and Drug Administration  allowed marketing of the first hand-held device intended to aid in the detection of life-threatening bleeding in the skull called intracranial hematomas, using near-infrared spectroscopy.]]></description>
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<title>U.S. Marshals seize products containing banned ephedrine for dietary supplements </title>
<link>http://www.drugsfreelist.com/medical_media_news/6347/U_S__Marshals_seize_products_containing_banned_ephedrine_for_dietary_supplements_</link>
<description><![CDATA[At the request of the U.S. Food and Drug Administration, U.S. Marshals  seized raw materials imported by Infinity Marketing Group, Inc. containing ephedrine alkaloids, a large family of pharmacological compounds called sympathomimetics banned by FDA since 2004 for use in dietary supplements.]]></description>
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<title>FDA, FTC act to remove “homeopathic” HCG weight loss products from the market</title>
<link>http://www.drugsfreelist.com/medical_media_news/6346/FDA,_FTC_act_to_remove_“homeopathic”_HCG_weight_loss_products_from_the_market</link>
<description><![CDATA[The U.S. Food and Drug Administration and the Federal Trade Commission (FTC) issued seven Warning Letters to companies marketing over-the counter (OTC) HCG products that are labeled as “homeopathic” for weight loss.]]></description>
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<title>FDA Drug Safety Communication: Safety Review Update of Medications used to treat Attention-Deficit/Hyperactivity Disorder (ADHD) in adults</title>
<link>http://www.drugsfreelist.com/medical_media_news/6345/FDA_Drug_Safety_Communication:_Safety_Review_Update_of_Medications_used_to_treat_Attention-Deficit_Hyperactivity_Disorder__ADHD__in_adults</link>
<description><![CDATA[The U.S. Food and Drug Administration (FDA) is updating its communication on the ongoing cardiovascular safety review of medications used for treating Attention-Deficit/Hyperactivity Disorder (ADHD), many of which are known to increase heart rate and blood pressure. ]]></description>
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<title>FDA Drug Safety Communication: Safety review of post-market reports of serious bleeding events with the anticoagulant Pradaxa (dabigatran etexilate mesylate)</title>
<link>http://www.drugsfreelist.com/medical_media_news/6344/FDA_Drug_Safety_Communication:_Safety_review_of_post-market_reports_of_serious_bleeding_events_with_the_anticoagulant_Pradaxa__dabigatran_etexilate_mesylate_</link>
<description><![CDATA[The U.S. Food and Drug Administration (FDA) is evaluating post-marketing reports of serious bleeding events in patients taking Pradaxa (dabigatran etexilate mesylate).]]></description>
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<title>FDA Drug Safety Communication: Modified Risk Evaluation and Mitigation Strategies (REMS) for Nplate (romiplostim) and Promacta (eltrombopag)</title>
<link>http://www.drugsfreelist.com/medical_media_news/6343/FDA_Drug_Safety_Communication:_Modified_Risk_Evaluation_and_Mitigation_Strategies__REMS__for_Nplate__romiplostim__and_Promacta__eltrombopag_</link>
<description><![CDATA[The U.S. Food and Drug Administration (FDA) has approved modifications to the Risk Evaluation and Mitigation Strategies (REMS) for platelet-booster drugs Nplate (romiplostim) injection and Promacta (eltrombopag) tablets.]]></description>
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<title>FDA. New and Generic Drug Approvals - December 13, 2011</title>
<link>http://www.drugsfreelist.com/medical_media_news/6342/FDA__New_and_Generic_Drug_Approvals_-_December_13,_2011</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date December 13, 2011 ]]></description>
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<title>FDA. New and Generic Drug Approvals - December 12, 2011</title>
<link>http://www.drugsfreelist.com/medical_media_news/6341/FDA__New_and_Generic_Drug_Approvals_-_December_12,_2011</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date December 12, 2011 ]]></description>
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<title>FDA. New and Generic Drug Approvals - December 9, 2011</title>
<link>http://www.drugsfreelist.com/medical_media_news/6340/FDA__New_and_Generic_Drug_Approvals_-_December_9,_2011</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date December 9, 2011 ]]></description>
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<title>FDA. New and Generic Drug Approvals - December 8, 2011</title>
<link>http://www.drugsfreelist.com/medical_media_news/6339/FDA__New_and_Generic_Drug_Approvals_-_December_8,_2011</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date December 8, 2011 ]]></description>
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<title>FDA. New and Generic Drug Approvals - December 7, 2011</title>
<link>http://www.drugsfreelist.com/medical_media_news/6338/FDA__New_and_Generic_Drug_Approvals_-_December_7,_2011</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date December 7, 2011 ]]></description>
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<title>FDA. New and Generic Drug Approvals - December 6, 2011</title>
<link>http://www.drugsfreelist.com/medical_media_news/6337/FDA__New_and_Generic_Drug_Approvals_-_December_6,_2011</link>
<description><![CDATA[New drugs approved.List of drugs approved by FDA to date December 6, 2011 ]]></description>
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<title>Roche`s cobas EGFR Mutation Test For Personalized Treatment Of Non-Small Cell Lung Cancer Receives CE Mark</title>
<link>http://www.drugsfreelist.com/medical_media_news/6336/Roche`s_cobas_EGFR_Mutation_Test_For_Personalized_Treatment_Of_Non-Small_Cell_Lung_Cancer_Receives_CE_Mark</link>
<description><![CDATA[Roche  announced  that the cobas EGFR Mutation Test is now CE marked for commercial availability in Europe and other countries that recognize CE mark.]]></description>
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<title>Long-term use of antiepileptic drug Vimpat® (lacosamide) reduced seizure frequency and severity and improved health-related quality of life measures</title>
<link>http://www.drugsfreelist.com/medical_media_news/6335/Long-term_use_of_antiepileptic_drug_Vimpat®__lacosamide__reduced_seizure_frequency_and_severity_and_improved_health-related_quality_of_life_measures</link>
<description><![CDATA[UCB announced new findings for Vimpat® (lacosamide) that offer additional support regarding the long-term effects of the antiepileptic drug (AED) as an adjunctive therapy for adults with uncontrolled partial-onset seizures.]]></description>
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