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WHO Drug Information Vol. 28 No. 2 2014.

By: Organization, World Health.
Material type: materialTypeLabelBookPublisher: Geneva : World Health Organization, 2014Copyright date: �2014Description: 1 online resource (171 pages).Content type: text Media type: computer Carrier type: online resourceISBN: 9789240693326.Subject(s): Drugs -- Standards -- Periodicals | Pharmaceutical industry -- Periodicals | Pharmaceutical preparations -- Standards -- PeriodicalsGenre/Form: Electronic books.DDC classification: 615.13 Online resources: Click to View
Contents:
Cover -- Contents -- Regulatory harmonization -- WHO collaboration with world pharmacopoeias -- Technologies, standards and norms -- Quality standards for pharmaceutical products -- Essential medicines -- Intensified efforts required to withdraw oral artemisinin-based monotherapies -- Safety and efficacy news -- Substandard and falsified products -- Falsified antimalarial medicines in West and Central Africa -- Stolen trastuzumab, pemetrexed and infliximab in Europe -- Safety Information -- Diacerein-containing medicines: restricted use -- Domperidone: adverse effects on the heart -- Hydroxyethyl starch-containing products: increased risk for patients with sepsis -- Epidural corticosteroid injection: rare but serious neurologic problems -- Zolpidem, eszopiclone: impaired next-day alertness -- Mirtazapine: abnormal heart rhythm -- Vemurafenib: liver problems -- Filgrastim and pegfilgrastim: capillary leak syndrome -- Belimumab: opportunistic brain infection -- Temozolomide: liver injury -- RAS-acting agents: not to be used in combination -- TNF-alpha inhibitors: reactivation of tuberculosis -- Arsenic-containing dental pastes: genotoxicity -- Serotonin-blocking medicines: serotonin syndrome -- Panitumumab: rare but severe skin reactions -- Reviews started -- Overview of safety reviews started -- Regulatory news -- Pre-marketing assessment -- EMA launches adaptive licensing pilot project -- EMA and TGA strengthen collaboration on orphan medicines -- MHRA introduces early access to medicines scheme -- EMA publishes draft guidelines for parallel scientific advice with health-technology-assessment bodies -- Clinical trials -- First-in-world pilot programme on multi-regional clinical trials -- EU votes in new rules for clinical trials -- EMA and FDA propose joint clinical investigation mechanism for rare children's disease -- Post-marketing control.
EU adopts specifications for post-marketing efficacy studies -- EMA reports on implementation of new pharmacovigilance legislation -- Guidance -- EMA recommendations on seasonal influenza vaccine composition -- MHRA confirms position on statins -- Approvals -- Miltefosine for leishmaniasis -- Apremilast for psoriatic arthritis -- Vintafolide for ovarian cancer, with diagnostic medicines etarfolatide and folic acid -- Siltuximab for Castleman's disease -- Vedolizumab for ulcerative colitis and Crohn's disease -- Empagliflozin for type 2 diabetes -- Simeprevir for chronic hepatitis C -- Fluticasone furoate and vilanterol trifenatate for asthma and COPD -- Generic oseltamivir for influenza -- Topiramate for migraine prevention in adolescents -- Long-acting recombinant coagulation factor IX concentrate for haemophilia B -- Albiglutide for type 2 diabetes -- Two sublingual pollen extracts for allergies -- Ramucirumab for stomach cancer -- Ceritinib for late-stage lung cancer -- Trametinib for advanced melanoma -- Vorapaxar to reduce cardiovascular risks -- Dalbavancin for skin infections -- Ataluren for Duchenne muscular dystrophy -- Obinutuzumab for chronic lymphocytic leukaemia -- Peginterferon beta-1a for multiple sclerosis -- Simoctogog alfa for patients with haemophilia A -- Brinzolamide / brimonidine tartrate to reduce intra-ocular eye pressure -- Publications and events -- Public health topics -- WHO hepatitis C guidelines published -- WHO report reveals worldwide antibiotic resistance -- EU and US continue joint battle against antimicrobial resistance -- WHO core functions need reliable funding -- WHO and Global Fund strengthen partnership -- Sixty-seventh World Health Assembly held -- Market and supply -- ViiV and MPP sign licence agreement for dolutegravir -- Global Fund meets with Chinese pharmaceutical manufacturers.
First WHO GMP-compliant Nigerian manufacturer -- Snapshot of patents and licences on antiretrovirals -- Antiretroviral prices in middle-income countries -- WHO prequalifies first products manufactured in Egypt -- BRICS Ministers join forces for access to medicines -- Upcoming events -- 16th International Conference of Drug Regulatory Authorities (ICDRA) -- WHO-UNICEF-UNFPA meeting with manufacturers -- WHO working for you -- Online database of training activities -- Consultation documents -- The International Pharmacopoeia -- Radiopharmaceuticals: General monograph -- Sodium iodide ([sup(131)]I) capsules -- Iobenguane ([sup(131)]) injection -- Fluconazole capsules -- Fluconazole injection -- Levamisole hydrochloride -- Dextromethorphan hydrobromide -- ATC/DDD Classification -- ATC/DDD Classification (Temporary) -- ATC/DDD Classification (Final) -- International Nonproprietary Names -- Proposed List No. 111.
Summary: WHO Drug Information communicates pharmaceutical information that is either developed and issued by WHO or transmitted to WHO by research and regulatory agencies throughout the World. The journal also includes regular presentations of newly proposed and recommended International Nonproprietary Names (INN) for Pharmaceuticals Substances. This volume contains the proposed INN List No.111.
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Cover -- Contents -- Regulatory harmonization -- WHO collaboration with world pharmacopoeias -- Technologies, standards and norms -- Quality standards for pharmaceutical products -- Essential medicines -- Intensified efforts required to withdraw oral artemisinin-based monotherapies -- Safety and efficacy news -- Substandard and falsified products -- Falsified antimalarial medicines in West and Central Africa -- Stolen trastuzumab, pemetrexed and infliximab in Europe -- Safety Information -- Diacerein-containing medicines: restricted use -- Domperidone: adverse effects on the heart -- Hydroxyethyl starch-containing products: increased risk for patients with sepsis -- Epidural corticosteroid injection: rare but serious neurologic problems -- Zolpidem, eszopiclone: impaired next-day alertness -- Mirtazapine: abnormal heart rhythm -- Vemurafenib: liver problems -- Filgrastim and pegfilgrastim: capillary leak syndrome -- Belimumab: opportunistic brain infection -- Temozolomide: liver injury -- RAS-acting agents: not to be used in combination -- TNF-alpha inhibitors: reactivation of tuberculosis -- Arsenic-containing dental pastes: genotoxicity -- Serotonin-blocking medicines: serotonin syndrome -- Panitumumab: rare but severe skin reactions -- Reviews started -- Overview of safety reviews started -- Regulatory news -- Pre-marketing assessment -- EMA launches adaptive licensing pilot project -- EMA and TGA strengthen collaboration on orphan medicines -- MHRA introduces early access to medicines scheme -- EMA publishes draft guidelines for parallel scientific advice with health-technology-assessment bodies -- Clinical trials -- First-in-world pilot programme on multi-regional clinical trials -- EU votes in new rules for clinical trials -- EMA and FDA propose joint clinical investigation mechanism for rare children's disease -- Post-marketing control.

EU adopts specifications for post-marketing efficacy studies -- EMA reports on implementation of new pharmacovigilance legislation -- Guidance -- EMA recommendations on seasonal influenza vaccine composition -- MHRA confirms position on statins -- Approvals -- Miltefosine for leishmaniasis -- Apremilast for psoriatic arthritis -- Vintafolide for ovarian cancer, with diagnostic medicines etarfolatide and folic acid -- Siltuximab for Castleman's disease -- Vedolizumab for ulcerative colitis and Crohn's disease -- Empagliflozin for type 2 diabetes -- Simeprevir for chronic hepatitis C -- Fluticasone furoate and vilanterol trifenatate for asthma and COPD -- Generic oseltamivir for influenza -- Topiramate for migraine prevention in adolescents -- Long-acting recombinant coagulation factor IX concentrate for haemophilia B -- Albiglutide for type 2 diabetes -- Two sublingual pollen extracts for allergies -- Ramucirumab for stomach cancer -- Ceritinib for late-stage lung cancer -- Trametinib for advanced melanoma -- Vorapaxar to reduce cardiovascular risks -- Dalbavancin for skin infections -- Ataluren for Duchenne muscular dystrophy -- Obinutuzumab for chronic lymphocytic leukaemia -- Peginterferon beta-1a for multiple sclerosis -- Simoctogog alfa for patients with haemophilia A -- Brinzolamide / brimonidine tartrate to reduce intra-ocular eye pressure -- Publications and events -- Public health topics -- WHO hepatitis C guidelines published -- WHO report reveals worldwide antibiotic resistance -- EU and US continue joint battle against antimicrobial resistance -- WHO core functions need reliable funding -- WHO and Global Fund strengthen partnership -- Sixty-seventh World Health Assembly held -- Market and supply -- ViiV and MPP sign licence agreement for dolutegravir -- Global Fund meets with Chinese pharmaceutical manufacturers.

First WHO GMP-compliant Nigerian manufacturer -- Snapshot of patents and licences on antiretrovirals -- Antiretroviral prices in middle-income countries -- WHO prequalifies first products manufactured in Egypt -- BRICS Ministers join forces for access to medicines -- Upcoming events -- 16th International Conference of Drug Regulatory Authorities (ICDRA) -- WHO-UNICEF-UNFPA meeting with manufacturers -- WHO working for you -- Online database of training activities -- Consultation documents -- The International Pharmacopoeia -- Radiopharmaceuticals: General monograph -- Sodium iodide ([sup(131)]I) capsules -- Iobenguane ([sup(131)]) injection -- Fluconazole capsules -- Fluconazole injection -- Levamisole hydrochloride -- Dextromethorphan hydrobromide -- ATC/DDD Classification -- ATC/DDD Classification (Temporary) -- ATC/DDD Classification (Final) -- International Nonproprietary Names -- Proposed List No. 111.

WHO Drug Information communicates pharmaceutical information that is either developed and issued by WHO or transmitted to WHO by research and regulatory agencies throughout the World. The journal also includes regular presentations of newly proposed and recommended International Nonproprietary Names (INN) for Pharmaceuticals Substances. This volume contains the proposed INN List No.111.

Description based on publisher supplied metadata and other sources.

Electronic reproduction. Ann Arbor, Michigan : ProQuest Ebook Central, 2022. Available via World Wide Web. Access may be limited to ProQuest Ebook Central affiliated libraries.

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