Izindaba Zenkampani
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Siyakuhalalisela!!
Sihalalisela ukuthi Thina, i-Changzhou Pharmaceutical Factory sithole Isitifiketi Sokubhaliswa Komkhiqizo nguMnyango Wezempilo wase-Republic of the Philippines ngamathebulethi ethu e-Rosuvastatin (5mg, 10mg, 20mg, 40mg), kanye nokubhaliswa NO. kukhona DR-XY48615, DR-XY48616, DR-XY...Funda kabanzi -
KONKE NGE-HYDROCHLOROTHIAZIDE
Abakhiqizi be-Hydrochlorothiazide bachaza yonke into ebalulekile nge-hydrochlorothiazide ukuze bakusize wazi kangcono ngayo. Iyini i-hydrochlorothiazide? IHydrochlorothiazide (HCTZ) iyi-thiazide diuretic esiza ukuvikela umzimba wakho ekumunceni usawoti omningi, onga ...Funda kabanzi -
Umuthi ohlosiwe wokwelapha i-myelofibrosis: i-Ruxolitinib
I-Myelofibrosis (MF) ibizwa ngokuthi i-myelofibrosis. Kuphinde kube yisifo esiyivelakancane kakhulu. Futhi imbangela ye-pathogenesis yayo ayaziwa. Izimpawu zomtholampilo ezijwayelekile amangqamuzana egazi abomvu ezingane kanye ne-juvenile granulocytic anemia enenombolo ephezulu yokwehla kwezinyembezi amangqamuzana egazi abomvu...Funda kabanzi -
Kufanele wazi okungenani lawa maphuzu angu-3 mayelana ne-rivaroxaban
Njenge-anticoagulant yomlomo entsha, i-rivaroxaban isetshenziswe kabanzi ekuvimbeleni nasekwelapheni isifo se-venous thromboembolic kanye nokuvimbela isifo sohlangothi ku-non-valvular atrial fibrillation. Ukuze usebenzise i-rivaroxaban ngokunengqondo, kufanele wazi okungenani lawa maphuzu ama-3....Funda kabanzi -
I-Changzhou Pharmaceutical ithole imvume yokukhiqiza ama-Lenalidomide Capsules
I-Changzhou Pharmaceutical Factory Ltd., inkampani ephethwe yi-Shanghai Pharmaceutical Holdings, ithole Isitifiketi Sokubhaliswa Kwezidakamizwa (Isitifiketi No. 2021S01077, 2021S01078, 2021S01079) esikhishwe i-State Drug Administration ye-Lenalidomide (Specification5 CapsuleFunda kabanzi -
Yiziphi izinyathelo zokuphepha zamaphilisi e-rivaroxaban?
I-Rivaroxaban, njenge-anticoagulant yomlomo entsha, isetshenziswe kabanzi ekuvimbeleni nasekwelapheni izifo ze-venous thromboembolic. Yini okudingeka ngiyinake lapho ngithatha i-rivaroxaban? Ngokungafani ne-warfarin, i-rivaroxaban ayidingi ukuqapha kwe-clotting indica ...Funda kabanzi -
2021 Ukugunyazwa Okusha Kwezidakamizwa kwe-FDA 1Q-3Q
Ukuqamba okusha kuqhubekisela phambili inqubekelaphambili. Uma kuziwa ekwenziweni okusha ekuthuthukisweni kwemithi emisha nemikhiqizo yebhayoloji yokwelapha, Isikhungo Sezidakamizwa Sokuhlola Nokucwaninga (CDER) se-FDA sisekela imboni yezokwelapha kuzo zonke izinyathelo zenqubo. Ngokuqonda kwayo ...Funda kabanzi -
Ukuthuthukiswa kwakamuva kwe-Sugammadex Sodium esikhathini sokuvuka kwe-anesthesia
I-Sugammadex Sodium iyisitha esiphikisayo se-non-depolarizing muscle relaxants (ama-myorelaxants), eyabikwa okokuqala kubantu ngo-2005 futhi kusukela ngaleso sikhathi yasetshenziswa emtholampilo eYurophu, e-United States naseJapane. Uma kuqhathaniswa nezidakamizwa zendabuko ze-anticholinesterase...Funda kabanzi -
Yiziphi izimila ezisebenza ngempumelelo ekwelapheni i-thalidomide!
I-Thalidomide iyasebenza ekwelapheni lezi zimila! 1. Lapho izimila eziqinile zingasetshenziswa khona i-thalidomide. 1.1. umdlavuza wamaphaphu. 1.2. Umdlavuza wendlala yesinye. 1.3. umdlavuza we-nodal rectal. 1.4. i-hepatocellular carcinoma. 1.5. Umdlavuza wesisu. ...Funda kabanzi -
Umbukiso we-Guangzhou API ngo-2021
I-86th China International Pharmaceutical Raw Materials/Intermediates/Packaging/Equipment Fair (i-API China kafushane) Umhleli: Reed Sinopharm Exhibition Co., Ltd. Isikhathi sombukiso: Meyi 26-28, 2021 Indawo: I-China Import and Export Fair Complex (Guangzhou) Isikali sombukiso: 60,000 square metres Ex...Funda kabanzi -
I-Obeticholic acid
Ngomhla zingama-29 kuNhlangulana, i-Intercept Pharmaceuticals yamemezela ukuthi isithole isicelo esisha esiphelele sesidakamizwa esivela e-US FDA mayelana ne-FXR agonist obeticholic acid (OCA) ye-fibrosis ebangelwa incwadi yokuphendula engeyona eyotshwala ye-steatohepatitis (NASH) (CRL). I-FDA isho ku-CRL ukuthi ngokusekelwe kudatha...Funda kabanzi -
I-Remdesivir
Ngomhla zingama-22 kuMfumfu, isikhathi saseMpumalanga, i-FDA yaseMelika igunyaze ngokusemthethweni i-antiviral Veklury (remdesivir) yaseGileyadi ukuthi isetshenziswe kubantu abadala abaneminyaka eyi-12 nangaphezulu futhi enesisindo okungenani esingama-40 kg abadinga ukulaliswa esibhedlela kanye nokwelashwa kwe-COVID-19. Ngokusho kwe-FDA, iVeklury njengamanje ukuphela kwe-COVID-19 egunyazwe yi-FDA ...Funda kabanzi