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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 Squibb , European Medicines Agency , European Commission , Committee For Medicinal Products Human Use , Medicinal Products , Human Use , Hiv Infection , Hiv Disease , Hiv Antiretroviral Therapy , Ntiretroviral Therapy For Hiv , Hiv Therapy , Niv Art , Protease Inhibitor , Rt Protease Inhibitor , Combination Drug Therapy , Drug Treatment Safety , Drug Safety , Treatment Safety , Acquired Immune Deficiency Syndrome ,

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 States , Hayley Thompson , Peter Wu , Emily Austin , Toronto Drug Checking Service , Drug Checking Service , Division Of Clinical Pharmacology , Canadian Medical Association Journal , University Of Toronto , Clinical Pharmacology , Canadian Medical Association , Medscape Medical News , Drug Treatment Safety , Drug Safety , Treatment Safety , Wound Management , Wound Care , Rug Overdose , Fairway Management , Anagement Of The Airway , Health Services , Health Care Services , V Intravenous ,

No Increased Blood-Related Side Effects With Radium-223 in Prostate Cancer

Patients with metastatic castration-resistant prostate cancer previously treated with external beam radiation therapy did not increase incidence of blood-related side effects with radium-223 compared with the overall population. ....

United States , Treatment Safety , Side Effects , Second Primary Malignancies , United States Based , Genitourinary Cancers Symposium , Prostate Cancer ,

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 Use , Pharmacovigilance Risk Assessment Committee , European Medicines Agency , European Commission , European Union , Medicinal Products , Human Use , Medicines Containing , Risk Assessment Committee , Drug Treatment Safety , Drug Safety , Treatment Safety , Drug Regulation , Drug Registries , Drug Registry , Rare Diseases , Prescription Drug , Cough And Cold Preparation Toxicity , Ough And Cold Preparation Overdose , Nt Specialty , Ead And Neck Surgery Ent Speciality , Pain Management , Ainful Joint , Joint Pain , Back Pain ,

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 States , Shounak Dasgupta , Tasim Zahid , Christy Santhosh , Khushi Mandowara , Sriparna Roy , European Union , Drug Administration , Nt Specialty , Ead And Neck Surgery Ent Speciality , Chronic Cough , Us Food And Drug Administration , Nited States Food And Drug Administration , Drug Treatment Safety , Drug Safety , Treatment Safety , Patient Safety ,