Mankhwala osakanizidwa amapezeka kwambiri ku US Popeza chifuwa ndi chizindikiro chofala cha matenda ambiri, zimveka kuti anthu akufuna mankhwala omwe angapange. izo. imani . Pali zambiri zakuthandizira suppressants zopezeka pamsika komanso zina zomwe zimapezeka ndi mankhwala okhaokha.
Pamwamba pa Zosankha Zotsutsa
Kupweteketsa kwambiri , komwe kumakhala ndi mankhwala otchedwa dextromethorphan , kumakhala kosawoneka bwino koma kungakhale kothandiza kwa chifuwa chaching'ono.
Omwe amawatsutsa ndi mtundu wa mankhwala omwe sasiya chifuwa koma amamasula ntchentche, kuti chifuwa chikhale chopindulitsa kwambiri.
Nthawi Yomwe Muwone Dokotala
Ngati muli ndi chifuwa choopsa kapena chokhazikika chomwe chimatenga nthawi yaitali kuposa masabata atatu, chiyenera kuyesedwa ndi wothandizira zaumoyo komanso mankhwala a chifuwa chotsekemera ayenera kugwiritsidwa ntchito pokhapokha ngati mukufunikira. Mabala-makamaka chifuwa chachikulu-angayambitse zinthu zanga zambiri ndipo ndibwino kuyesa kuchiza chomwe chimayambitsa m'malo moyesera kuziphimba. Izi zimaphatikizapo zambiri osati kungotenga mankhwala kuti chifuwa chisayime.
Kumene Mavuto Amabodza
Zaka zaposachedwapa, pakhala vuto lalikulu la chifuwa chogonjetsa presressants pamene akuuzidwa ndi kugulitsidwa ngati sakuvomerezedwa ndi FDA. Pakalipano, pali mankhwala asanu ndi awiri okha omwe amavomerezedwa ndi FDA. Zikuphatikizapo:
- Tussicaps
- Tussionex Pennkinetic
- Mzinda wa Hydrocodone
- Mycodone
- Mankhwala otchedwa Methylbromide ndi Hydrocodone
- Fikodani
- Tussigon
Zonsezi zimaphatikizapo opiate (hydrocodone) yomwe yatsimikiziridwa kuti imatha kuyendetsa chifuwa kwa akulu ndi ana oposa 6. Komabe, ayenera kupewa ndi anthu omwe angakhale akuyambiranso kuledzera kwa opioids chifukwa Ndibwino kuti muthetse kachifuwa.
Mankhwalawa ayenera kugwiritsidwa ntchito kwa akuluakulu ndi ana opitirira zaka zisanu ndi chimodzi . Ena mwa iwo akugulitsidwa ndipo ali ndi malangizo a dosing kwa ana ngati aang'ono 2. Komabe, a FDA adanena kuti mankhwalawa sali otetezeka ndipo sayenera kugwiritsidwa ntchito kwa ana osapitirira zaka 6.
Kugwiritsira ntchito mankhwala "pa label" siwatsopano ndipo sizomwe si zachilendo, makamaka pa ana. Mavuto ochepa chabe a mankhwalawa amachitikira ana chifukwa chakuti anthu ambiri safuna kuti alembe ana awo "mankhwala" akuyesa kuti ayesedwe ndizovuta kwambiri kusiyana ndi akuluakulu. Mwamwayi, palibe zolimbikitsa zambiri (ndalama) mmenemo kwa opanga mankhwala.
Koma kupatsa ana mankhwala a chifuwa cha mankhwalawa ndi koopsa. Angathe kupuma kupuma ku zoopsa komanso akhoza kufa.
Vuto lina lalikulu ndilokuti mankhwala ena amodzi akugulitsidwa kuti agwiritse ntchito zizindikiro zambiri. A FDA amavomereza kuti chifuwa chokhachokha chimaphatikizidwe ndi mankhwala a hydrocodone ndi osokoneza bongo. Mankhwala aliwonse omwe amaphatikizapo zinthu zina (monga expectorant kapena decongestant) sakuvomerezedwa ndi FDA ndipo sayenera kulamulidwa kapena kugulitsidwa ku United States.
Dokotala Wanu Sanadziwe
Gawo loopsya kwambiri la vutoli ndilo kuti ambiri omwe amapereka chithandizo chamankhwala sankadziwa mankhwalawa sanalandiridwe ndipo akhala akuwafotokozera. Awa si mankhwala omwe mungagule pa "msika wakuda" kapena kudzera mu intaneti. Ndi mankhwala omwe mungapereke kwa dokotala wanu ndikugula ku pharmacy yanu.
A FDA sakufotokoza zochitika zilizonse zovuta ndi mankhwalawa (kupatula ngati apatsidwa kwa ana osapitirira 6) kotero pali zovuta zochepa zomwe zachitika. Komabe, zoona zake ndi kuti mankhwalawa apangidwa ndi kugulitsidwa ndipo sanavomerezedwe.
Kuyambira pa March 31st, 2008 makampani onse omwe amapanga mankhwalawa analamulidwa kuti asiye kupanga ndi kugulitsa. Pambuyo pa tsikulo, ngati kampani ikugulitsabe zinthuzi, akhoza kukumana ndi chilango kuchokera ku FDA.
Zotsatira:
"Mafunso ndi Mayankho Okhudza Ntchito Yogwirizira ya FDA Ponena za mankhwala Osokoneza Bongo Opangidwa ndi Mankhwala Osokoneza Bongo." US Administration and Drug Administration 01 Oct 07.
"Madokotala a FDA Alert on Tussionex, Long-Acting Acting Medicine Cough Medicine Ali ndi Hydrocodone." FDA News Press Release 11 Mar 08. US Food and Drug Administration Administration.