Drug alert versi WHO


Di bawah ini adalah beberapa obat yang masuk ke dalam daftar drug alert versi WHO, sampai 22 Januari 2012 sudah mencapai 124 obat. Daftar dari urutan 100-124 diantaranya:


  • Drug Alert 124
    A/H1N1 vaccination safety: new safety surveillance tool available
  • Drug Alert 123
    Dextropropoxyphene-containing medicines to be withdrawn from European market
  • Drug Alert 122
    Warning on purchase of antivirals without a prescription, including via the Internet
  • Drug Alert 121
    Marketing authorization of efalizumab in the European Union to be suspended due to safety concerns
  • Drug Alert 120
    Toremifene should not be used in patients at risk of QT-prolongation or other heart problems: recommendation from the European Medicines Agency
  • Drug Alert 119
    Marketing authorization for rimonabant to be suspended across the European Union since the benefits of the medicine do not outweigh its risks
  • Drug Alert 118
    Contaminant detected in heparin material of specified origin in the USA and in Germany; serious adverse events reported; recall measures initiated
  • Drug Alert 117
    Antimalarial chlorproguanil-dapsone (LapDap™) withdrawn following demonstration of post-treatment haemolytic anaemia in G6PD deficient patients in a Phase III trial of chlorproguanil-dapsone-artesunate (Dacart™) versus artemether-lumefantrine (Coartem®) and confirmation of findings in a comparative trial of LapDap™ versus Dacart ™
  • Drug Alert 116
    Veralipride (The European Medicines Agency (EMEA) has issued a Press Release recommending the withdrawal of the marketing authorization for all medicinal products containing veralipride).
  • Drug Alert 115
    Vincristine (chemotherapeutic agent)
  • Drug Alert 114
    (All batches of Viracept (nelfinavir) recalled from the European Market due to possible contamination with a genotoxic substance)
  • Drug Alert 113
    (Oral nimesulide: marketing suspended in Ireland due to reports of liver failure)
  • Drug Alert 112
    (Levaquin {levofloxacin} injection {25 mg/ml 20 ml vials, Batch Nos. 6CB5W00, 6CB6100; Expiry February 2008}: product likely intended for black market use; public health hazard)
  • Drug Alert 111
    (Cyclooxygenase-2 {COX-2} Inhibitor Medicines)
  • Drug Alert 110
    {Counterfeit triple antiretroviral combination product (Ginovir 3D) detected in Côte d’Ivoire}
  • Drug Alert 109
    {Virologic failure in HIV patients treated with the combination of Didanosine, Lamivudine and Tenofovir}
  • Drug Alert 108
    {Suspension of Manufacturing Licence held by Pan Pharmaceuticals Limited, Sydney}
  • Drug Alert 107
    {Important safety update on lepirudin (Refludan) following reports of fatal anaphylactic reactions}
  • Drug Alert 106
    {Risk of serious hypersensitivity and skin reactions with parecoxib sodium The European Medicines Evaluation Agency (EMEA) has issued a public statement}
  • Drug Alert 105
    {Olanzapine: associations with hyperglycemia resulting in diabetic ketoacidosis and coma}
  • Drug Alert 104
    {Rapid Alert Notification of a Quality Defect in Prednisolone- Gentamicin (Pred-G) Eye Drops}
  • Drug Alert 103
    {Nonacog alfa (Benefix) : Intensive post-marketing surveillance and new clinical trials for additional data}
  • Drug Alert 102
    {Voluntary withdrawal of Cerivastatin – Reports of Rhabdomyolysis}
  • Drug Alert 101
    {Leflunomide – severe and serious hepatic reactions}
  • Drug Alert 100
    {Infliximab (Remicade) – reports of tuberculosis infections}


Dengan adanya drug alert ini diharapkan adanya pemantauan penggunaan obat atau high alert yang lebih awas, tidak hanya bagi obat yang sudah ditetapkan diatas saja tapi juga obat2an lainnya yang dicurigai dapat menimbulkan Adverse Drug Reactions (ADRs).


sumber: WHO, januari 2012

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