FDA Inoti Aya Ndiwo Imwe Kubata Kwausingafaniri Kushandisa

Zvemukati zvedu zvinotariswa nevashandi vedu vepamusoro-soro kuratidza chokwadi uye kuona kuti vaverengi vedu vanowana ruzivo rwakanaka uye zano rekuita sarudzo dzakangwara uye dzine hutano.
Isu tinotevera nhungamiro dzakarongwa dzekuwana ruzivo uye kubatanidza kune zvimwe zviwanikwa, kusanganisira tsvakiridzo yesainzi uye mabhuku ezvokurapa.

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Kana uchiita kuti vaunosangana navo vave chikamu chinokosha chemaitiro ako emangwanani, kufanana nekapu yako yekutanga yekofi, hausi wega.Maererano neCenters for Disease Control and Prevention (CDC), vanenge mamiriyoni makumi mana neshanu muUnited States vanopfeka lenses.
Zvakadaro, pane imwe mhando yekuona lens yausingafanire kushandisa - kana ukadaro, unogona kukanganisa chiono chako. Verenga kuti uone kuti ndedzipi mhando dzema lens dzinodziviswa zvakanyanya nevanoonana lens nyanzvi kuUS Food and Drug Administration. FDA).
Nepo vanhu vazhinji vachitenga nekushandisa over-the-counter lenzi gore rega rega pasina kukuvadzwa, kuita izvi kukungurutsa dhizi nguva dzese.
The FDA inoshuma kuti kushandisa over-the-counter lenzi kana kuashandisa zvisirizvo kunogona kucheka kana kukwenya mboni yeziso, kukonzeresa kusawirirana, kukonzeresa maziso kana kubuda mvura, kukonzeresa kutapukira, kukanganisa kuona, uye kutotungamirira kuupofu.
Kunyange zvingave zvinonakidza kushongedza maziso ako nemavara ekuonana lenzi, ingave yechiitiko chakakosha kana kungochinja chitarisiko chako, iyo FDA inoti zvakakosha kuti uwane iwo chaiwo malenzi emeso ako kuitira kudzivirira kukuvara kweziso.
Kuti uve nechokwadi chekuti unowana iwo chaiwo malenzi ekuonana, iyo FDA inokurudzira kuti iwe uongororwe ziso uye utore tsamba kubva kuna ane rezinesi ophthalmologist, kunyangwe yekushongedza lenzi, kuti uve nechokwadi chekuti anokodzera.
Nepo ma-over-the-counter lenzi anogona kunge achinyanya kukuvadza, malenzi emhando ipi neipi anogona kukanganisa hutano hweziso rako kana ukasateera zvimwe zviratidzo zvekunyevera.
Iva nechokwadi chekuonana nanachiremba kana ukaona kutsvuka, kuramba kurwadza kwemaziso, kubuda ropa, kana kusaona zvakanaka, sezvo izvi zvingava zviratidzo zvechirwere chemaziso.” Kana zvikasarapwa, utachiona hwemaziso hunogona kukomba uye huchiita kuti utadze kuona,” iyo FDA inonyevera.

Nepo iwe usinga fanire kutenga macontact lens zvakananga kubva kuna aphthalmologist, pane nzira yekusiyanisa zviri pamutemo vatengesi velens kubva kune vatengesi vanogona kunge vachikutengesa iwe zvigadzirwa zvisina kunaka.
Zvinoenderana nemirairo yeFDA, chero mutengesi welens ari pamutemo anokukumbira tsamba yelenzi uye bvunza chiremba wako asati akupa chigadzirwa. ”Havafanire kungokumbira gwaro, asi vanofanirwa kukumbirawo zita nefoni yachiremba wako. nhamba.Kana vakasabvunza ruzivo urwu, vari kutyora mutemo wemubatanidzwa uye vanogona kukutengesera zvisiri pamutemo lenzi, "FDA yakatsanangura.