Isidakamizwa sokunciphisa isisindo uBelviq uhoxisiwe emakethe yase-US phakathi kokukhathazeka kuphakamisa ingozi yomdlavuza

UBelviq — isidakamizwa esinciphisa isisindo — wasuswa emakethe yase-U.S. Ngenxa yesicelo sokuhoxa emakethe ye-FDA. Idatha ikhombise ukwanda komdlavuza okuqhathaniswa ne-placebo

I-FDA ivuma kuqala i-Eliquis generic: apixaban

Labo abasengozini yokushaywa unhlangothi kungekudala bazoba nenye indlela eshibhile esikhundleni sika-Eliquis, ocekela phansi igazi. I-FDA ivume izinhlobo ezi-2 ze-generic Eliquis (apixaban) ngoDisemba 2019.

I-FDA igunyaza u-Erleada, ukwelashwa okusha komdlavuza wendlala yesinye

I-Erleada iyisidakamizwa sokuqala esivunyelwe i-FDA samathumba amelana ne-hormone, angasabalali (ukumelana non-metastatic) —eziza njengezindaba ezamukelekile ezigulini ezinomdlavuza wesinye.

I-FDA igunyaza u-Ervebo, umuthi wokugoma wokuqala we-Ebola

U-Ervebo, umuthi wokugoma we-Ebola wokuqala emhlabeni uphawula ingqophamlando yezempilo yomphakathi ukuvikela kulesi sifo esithathelwanayo.

Konke esikwaziyo ngeFavilavir, ukwelashwa okungenzeka kube yi-coronavirus

UFavilavir umuthi olwa namagciwane osetshenziswa njengokwelashwa komkhuhlane eJapan futhi manje ubhekene nokuhlolwa komtholampilo nge-COVID-19 eChina.

I-FDA igunyaza okujwayelekile kweGilenya

NgoDisemba 5, 2019 i-U.S. Food and Drug Administration (FDA) yamemezela ukuvunywa kwe-fingolimod, uhlobo olujwayelekile lwe-Gilenya, umuthi owelapha i-MS.

Izinhlobo ezi-9 ezijwayelekile zeLyrica manje sezitholakala ngezindleko eziphansi zeziguli

I-FDA ivume izinhlobo ezi-9 ze-Lyrica generic (pregabalin) ukwehlisa izindleko zayo. I-anticonvulsant ejwayelekile ingabiza u- $ 320- $ 350 ngaphansi kwegama lomkhiqizo elithi Lyrica.

I-FDA igunyaza umuthi wokuqala ngomlomo wokopha kakhulu kusuka ku-uterine fibroids

Imishanguzo yomlomo izotholakala maduzane ukunciphisa ukopha okunzima kokuya esikhathini (menorrhagia) kusuka ku-uterine fibroids, ngenxa yokuvunywa kwe-FDA kwe-Oriahnn.

I-FDA ikhumbula amaphilisi wokukhishwa okwandisiwe kwe-metformin

NgoMeyi 2020, i-FDA yakhipha isaziso sokuzikhethela sokukhumbula amaphilisi e-metformin ER 500 mg. NgoJan. 4, 2021, ukukhululwa kwandiswa.

Funda ngemithi emisha emi-5 eza ngo-2020

I-FDA igunyaza imishanguzo emisha unyaka nonyaka. Abanye beza ngqo emakethe, kanti abanye bayabambezeleka. Lezi yizo ezijabulisa kakhulu endleleni.

Izidakamizwa ezijwayelekile zisanda kutholakala ngo-2019

Imithi engamashumi amane isitholakale njengemithi ejwayelekile ngo-2019. Bona ukuthi le mishanguzo ejwayelekile iqhathaniswa kanjani nozakwabo bomkhiqizo.

I-FDA idonsa zonke izinhlobo ze-ranitidine emakethe yase-U.S

Ungumsebenzisi weZantac noma i-generic yayo? Funda ukuthi lokhu kusho ukuthini kuwe njengoba amakhemisi eyekile ukunikeza amaphilisi ngenxa yokukhumbula i-ranitidine.

I-FDA igunyaza iQelbree, umuthi omusha ongavuseleli we-ADHD

I-Qelbree (viloxazine), umuthi wokuqala omusha ongavuseleli we-ADHD eminyakeni eyishumi, izotholakala ezigulini kwikota yesibili ka-2021.

I-FDA ivuma ukushintshwa kwe-Rx-to-OTC yelotion lotice yekhanda

Le lotion yentloko yezintwala eyakhishwa ngaphambilini kuphela, iSklice, isiyatholakala ngaphezu kwekhawunta.