Iindaba zeNkampani

  • Sivuyisana nawe!!

    Sivuyisana nawe!!

    Sivuyisana nathi, i-Changzhou Pharmaceutical Factory sifumene iSatifikethi sokuBhaliswa kweMveliso yiRiphabhliki yasePhilippines iSebe lezeMpilo kwiiRosuvastatin Tablets (5mg, 10mg, 20mg, 40mg), kunye nokubhaliswa NO. zi-DR-XY48615, DR-XY48616, DR-XY...
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  • KONKE NGEHYDROCHLOROTHIAZIDE

    KONKE NGEHYDROCHLOROTHIAZIDE

    Abavelisi beHydrochlorothiazide bachaza yonke into ebalulekileyo malunga ne-hydrochlorothiazide ukukunceda wazi ngcono ngayo. Yintoni i-hydrochlorothiazide? IHydrochlorothiazide (HCTZ) yithiazide diuretic enceda ekuthinteleni umzimba wakho ekufunxeni ityuwa eninzi kakhulu, enokuthi ...
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  • Ichiza ekujoliswe kulo unyango myelofibrosis: Ruxolitinib

    Ichiza ekujoliswe kulo unyango myelofibrosis: Ruxolitinib

    I-Myelofibrosis (MF) ibizwa ngokuba yi-myelofibrosis. Kwakhona sisifo esinqabileyo kakhulu. Kwaye unobangela we-pathogenesis yayo awaziwa. Iimpawu zeklinikhi eziqhelekileyo ziseligazi elibomvu lolutsha kunye ne-granulocytic anemia yolutsha enenani eliphezulu lokukrazula kweeseli ezibomvu zegazi ...
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  • Kufuneka wazi ubuncinane la manqaku e-3 malunga ne-rivaroxaban

    Kufuneka wazi ubuncinane la manqaku e-3 malunga ne-rivaroxaban

    Njenge-anticoagulant yomlomo omtsha, i-rivaroxaban isetyenziswe ngokubanzi ekukhuselweni kunye nokunyangwa kwesifo se-venous thromboembolic kunye nokukhusela i-stroke kwi-non-valvular atrial fibrillation. Ukuze usebenzise i-rivaroxaban ngokufanelekileyo, kufuneka wazi ubuncinane la manqaku e-3 ....
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  • IChangzhou Pharmaceutical ifumene imvume yokuvelisa iLenalidomide Capsules

    IChangzhou Pharmaceutical ifumene imvume yokuvelisa iLenalidomide Capsules

    I-Changzhou Pharmaceutical Factory Ltd., i-subsidiary ye-Shanghai Pharmaceutical Holdings, ifumene iSatifikethi sokuBhalisa iDrug (iSitifiketi esinguNombolo 2021S01077, 2021S01078, 2021S01079) esikhutshwe nguRhulumente woLawulo lweDrugs kwiLenalidomide ....
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  • Ziziphi izilumkiso zeepilisi ze-rivaroxaban?

    Ziziphi izilumkiso zeepilisi ze-rivaroxaban?

    I-Rivaroxaban, njenge-anticoagulant yomlomo omtsha, isetyenziswe ngokubanzi ekukhuseleni nasekunyangeni izifo ze-venous thromboembolic. Yintoni endiyidingayo ukuyiqwalasela xa ndithatha i-rivaroxaban? Ngokungafaniyo ne-warfarin, i-rivaroxaban ayifuni ukujongwa kwe-clotting indica ...
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  • Ngo-2021 i-FDA eVunyiweyo yeChiza eNtsha 1Q-3Q

    Utshintsho luqhubela phambili inkqubela. Xa kuziwa kubuchule obutsha kuphuhliso lwamachiza amatsha kunye neemveliso zonyango zebhayoloji, Iziko le-FDA loVavanyo lweZiyobisi kunye noPhando (CDER) lixhasa ishishini loxubo mayeza kuwo onke amanyathelo enkqubo. Ngokuqonda kwayo ...
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  • Uphuhliso lwakutsha nje lweSugammadex Sodium ngexesha lokuvuka kwe-anesthesia

    Uphuhliso lwakutsha nje lweSugammadex Sodium ngexesha lokuvuka kwe-anesthesia

    I-Sugammadex Sodium i-antagonist ye-novel ye-electroly non-depolarizing muscle relaxants (i-myorelaxants), eyaqala ukuxelwa ebantwini kwi-2005 kwaye sele isetyenziswe kwikliniki eYurophu, e-United States naseJapan. Xa kuthelekiswa namachiza emveli e-anticholinesterase...
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  • Yeyiphi ithumba i-thalidomide esebenzayo ekunyangeni!

    Yeyiphi ithumba i-thalidomide esebenzayo ekunyangeni!

    I-Thalidomide iyasebenza ekunyangeni la mathumba! 1. Apho amathumba aqinileyo anokuthi asetyenziswe i-thalidomide. 1.1. umhlaza wemiphunga. 1.2. Umhlaza wedlala lobudoda. 1.3. umhlaza wamaqhuqhuva. 1.4. hepatocellular carcinoma. 1.5. Umhlaza wesisu. ...
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  • Umboniso weGuangzhou API ngo-2021

    Umboniso weGuangzhou API ngo-2021

    I-86th China International Pharmaceutical Raw Materials / Intermediates/Packaging/Equipment Fair (API China ngokufutshane) Umququzeleli: Reed Sinopharm Exhibition Co., Ltd. Ixesha lokubonisa: NgoMeyi 26-28, 2021 Indawo: I-China yokungenisa kunye nokuThumela ngaphandle kweFayile Complex (Guangzhou) Isikali somboniso: 60,000 square metres Ex...
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  • Obeticholic acid

    NgoJuni 29, i-Intercept Pharmaceuticals ibhengeze ukuba ifumene isicelo esipheleleyo sechiza esivela kwi-US FDA malunga ne-FXR agonist obeticholic acid (OCA) ye-fibrosis ebangelwa yi-non-alcoholic steatohepatitis (NASH) I-Response letter (CRL). I-FDA ithe kwi-CRL ukuba isekwe kwidatha...
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  • I-Remdesivir

    Nge-22 ka-Okthobha, ixesha laseMpuma, i-FDA yaseMelika yamkele ngokusemthethweni iVeklury (remdesivir) yaseGiliyadi ukuba isetyenziswe kubantu abadala abaneminyaka eli-12 nangaphezulu kwaye banobunzima obungama-40 kg abafuna ukulaliswa esibhedlele kunye nonyango lwe-COVID-19. Ngokutsho kwe-FDA, iVeklury ngoku kuphela kwe-FDA evunywe yi-COVID-19 ...
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