6533b83afe1ef96bd12a71ca
RESEARCH PRODUCT
Three years of experience : the Italian registry and safety data update
Giovanni Luigi MancardiLaura PeriottoPier Giuseppe RossiM. De RosaR. IommelliNicola VanacoreCarlo PiccinniClara MilanesePatrizia PopoliAlice LaroniCarlo TominoRoberto D’alessandroMaria Giovanna MarrosuFilippo DragoM. R. TolaG. ComiA. CovezzoliAntonio BertolottoGiovanni SavettieriGioacchino TedeschiNicola MontanaroMaria Pia AmatoCarlo PozzilliL.m.e. GrimaldiLeandro Provincialisubject
AdultMalemedicine.medical_specialtyPediatricsMultiple SclerosisDermatologyDiseaseAntibodies Monoclonal HumanizedNatalizumabPharmacovigilanceProduct Surveillance PostmarketingmedicineHumansRegistriesAdverse effectbusiness.industryNatalizumabMultiple sclerosisGeneral Medicinemedicine.diseasePsychiatry and Mental healthItalyPHARMACOVIGILANCEREGISTRYsurveillance program; pharmacovigilance; multiple sclerosis; natalizumabPhysical therapyFemaleSettore MED/26 - NeurologiaNeurology (clinical)NeurosurgerybusinessMultiple sclerosis NatalizumabSurveillance program Pharmacovigilancemedicine.drugdescription
At the end of 2006, a pharmacovigilance program on natalizumab was settled by the Italian Pharmaceutical Agency, and on January 2007, multiple sclerosis patients poorly responding to the immunomodulating therapies or with an aggressive clinical form of disease from onset initiated to be registered and to receive the medication. On February 2010, almost 3,000 cases have been treated with natalizumab. The drop-out rate is 10%. Almost 800 cases received cycles of natalizumab for more than 18 months. One case of PML was reported and other adverse events are similar to those described in phase III studies. The majority of cases remained stable, while in 25% of cases, an improvement of disability was documented.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2011-01-01 |