Amachiza amanqabileyo aqhelekileyo e-US Njengoko ukukhwehlela kungumqondiso oqhelekileyo wezifo ezininzi, kuyaqondakala ukuba abantu bafuna unyango oluza kwenza. . ayeke . Kukho amaninzi amanqamlezo okukhupha amaninzi atholakalayo kwi-counter-counter-kunye ne-ezimbalwa ezifumanekayo ngomyalelo kuphela.
Ngaphezulu kweCandelo lokuCwangcisa
Ukunciphisa amanqaku angaphezu kwe-counter , okuqukethe umkhiqizo obizwa ngokuba ngu- dextromethorphan , uhlala ungasebenzi kakuhle kodwa unokunceda ukukhwehlela okuncinci.
Abaxhasi bahlobo lonyango aluyeki ukukhwehlela kodwa kunoko lukhulule i-mucus, okwenza ukukhwehlela kuvelise ngakumbi kwaye kusebenze.
Nini ukubona iDokotela
Ukuba unomkhuhlane onzima okanye ongapheliyo ohlala ixesha elide ngaphezu kweeveki ezintathu, kufuneka uhlolwe ngumniki-nkonzo wakho wezempilo kunye nokunciphisa umgca wokukhupha kufuneka usebenzise kuphela xa kudingekile. Iingqumbo-ngokukodwa ukukhwehlela okungapheliyo- zingabangela izinto zam ezininzi kwaye kukulungele ukuzama ukunyanga imbangela engakumbi kunokuzama ukuyibeka. Oku kuquka okungaphezulu nje kokuthatha iyeza ukuze wenze ukukhwehlela kumise.
Apho iNgxaki ilala khona
Kwiminyaka yakutshanje, kubekho ingxaki enkulu ekunciphiseni ukukhwehlela komzimba okumiselweyo kwaye kuthengiswa xa bengavunywanga yi-FDA. Okwangoku, kukho kuphela iindleko zokunciphisa umyalelo wokukhukhumeza ezivunyiweyo yi-FDA. Ziquka:
- Tussicaps
- Tussionex Pennkinetic
- Hydrocodone Compound
- Mycodone
- I-homatroprine i-Methylbromide ne-Hydrocodone i-Bitartrate
- Hycodan
- Tussigon
Zonke ezi zithintelo zokukhupha i-opiate (i-hydrocodone) ebonakaliswe ngempumelelo ekulawuleni umkhuhlane kubantu abadala kunye nabantwana abangaphezu kwe-6. Noko ke, kufuneka baphephe ngabantu abangase babuyiselwe kwi-addiction ye-opioids kuba kulungele umngcipheko wokuphindaphinda ukuphatha ukukhwehlela okulula.
La mayeza kufuneka asetyenziswe kuphela kubantu abadala kunye nabantwana abangaphezu kweminyaka engama-6 . Abanye babo bathengiswa kwaye banemiyalelo yokulandelela abantwana njengabantwana abancinci. Nangona kunjalo, i-FDA ichaze ukuba la mayeza awakhuselekile kwaye akufanele asetyenziswe abantwana abangaphantsi kweminyaka engama-6.
Ukusebenzisa imishanguzo "kwilebula" akuyinto entsha kwaye akukho konke okuqhelekanga, ngakumbi kwizonyango. Zimbalwa izilingo zamachiza ezenziwa kwiintsana ngenxa yokuba abantu abaninzi bafuna ukutyikitya abantwana babo kwiimvavanyo "zokulinga" kwaye ukufumana ezi zilingo kuvunywe nzima kunokuba zikhulile kubantu abadala. Ngelishwa, akukho nxalenye yokukhuthaza (imali) kuyo kubavelisi bamayeza.
Kodwa ukunikezela ngamachiza okukhwehlela imithi kubantwana kuyingozi. Baya kunciphisa ukuphefumla kwabo kumazinga anobungozi kwaye banokufa.
Enye ingxaki ebalulekileyo kukuba ezinye zokunciphisa i-prescription zidayiswa zijoliswe ekuphatheni iimpawu ezininzi. I-FDA iye yavuma kuphela ukunciphisa ukukhwehlela komzimba ukuba ifake i-hydrocodone kunye nomxinzelelo. Nawaphi na amayeza aquka ezinye izithako (ezifana nomxhasi okanye i-decongestant) ayivunywanga yi-FDA kwaye ayifanele ibekwe okanye athengiswe e-United States.
Ugqirha Akwazanga
Inxalenye ebaluleke kakhulu yile ngxaki kukuba abaninzi ababonelela ngempilo babengazi ukuba ezi zi yobisi azivunyelwanga kwaye ziye zazimisela. Ezi akuzona unyango onokuzithenga kuphela "kumarhwebo omnyama" okanye nge-intanethi. Ziyimishanguzo enokumiselwa ngugqirha wakho kwaye uthenge kwi-pharmacy yakho yangingqi.
I-FDA ayixeli naziphi na iziganeko ezichasayo ngala mayeza (ngaphandle kokuba unikezelwa abantwana abangaphantsi kwe-6) ngoko kuya kubakho ubunzima obuncinane obwenziweyo. Nangona kunjalo, inyaniso kukuba la mayeza ayenziwe kwaye athengiswa kwaye awazange avunywe.
Ngomhla ka-Matshi 31, 2008 zonke iinkampani ezenziwayo la mayeza ziye zalelwa ukuba ziyeke ukuvelisa nokuzithengisa. Emva kwaloo mhla, ukuba inkampani isayithengisa le mveliso, banokujamelana nezohlwayo ezivela kwi-FDA.
Imithombo:
"Imibuzo Neempendulo Ngomthetho Wokunyanzeliswa kwe-FDA Ngokuphathelele kwiMveliso yeDrrocodone engavumelekanga." US Food and Drug Administration 01 Oct 07.
"I-FDA Issues Alert kwi-Tussionex, i-Long-Acting Acting Medicine Cough Medicine equkethe i-Hydrocodone." I-FDA News Press Release 11 kuMatshi 08. Ukutya kwe-US kunye noLawulo lweeDrug.