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New Contraindications to Coadministration of Atazanavir

New restrictions have been imposed by the European Medicines Agency on the coadministration of the anti-HIV drug atazanavir with a variety of other agents.

Bristol myers squibbEuropean medicines agencyEuropean commissionCommittee for medicinal products human useMedicinal productsHuman useHiv infectionHiv diseaseHiv antiretroviral therapyNtiretroviral therapy for hivHiv therapyNiv artProtease inhibitorRt protease inhibitorCombination drug therapyDrug treatment safety

Xylazine Increasingly Found in Canada s Illegal Drug Supply

The drug, a tranquilizer for animals including horses and cattle, is hard for clinicians to identify, and users may not even know they have taken it.

United statesHayley thompsonPeter wuEmily austinToronto drug checking serviceDrug checking serviceDivision of clinical pharmacologyCanadian medical association journalUniversity of torontoClinical pharmacologyCanadian medical associationMedscape medical newsDrug treatment safetyDrug safetyTreatment safetyWound management

Europe Approves Neutropenia and Schizophrenia Treatments

Recommendations were also endorsed to institute measures to reduce risks from cold and flu medicines containing pseudoephedrine.

Committee for medicinal products human usePharmacovigilance risk assessment committeeEuropean medicines agencyEuropean commissionEuropean unionMedicinal productsHuman useMedicines containingRisk assessment committeeDrug treatment safetyDrug safetyTreatment safetyDrug regulationDrug registriesDrug registryRare diseases

US FDA Declines to Approve Merck s Chronic Cough Drug

The U.S. Food and Drug Administration (FDA) declined to approve Merck's drug for chronic cough, the company said on Wednesday, marking the second rejection in less than two.

United statesShounak dasguptaTasim zahidChristy santhoshKhushi mandowaraSriparna royEuropean unionDrug administrationNt specialtyEad and neck surgery ent specialityChronic coughUs food and drug administrationNited states food and drug administrationDrug treatment safetyDrug safetyTreatment safety

EMA Committee Recommends Label Update for Some Decongestants

The European Medicines Agency s safety committee on Friday recommended changes to product information for all medicines that contain the ingredient pseudoephedrine to address safety concerns related to neurological and heart-related side effects.

Pratik jainKrishna chandra eluriMcneil products ltdEuropean medicines agencyOrganon coReckitt benckiserPatient safetyDrug treatment safetyDrug regulationAdverse effectsSide effects

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