Kategoriya

retseptsiz sotiladigan

Faol modda

  • ambroksol gidroxloridi

Farmakoterapevtik guruh

  • R05CB06

Tibbiyot yo'nalishi

  • Yo'tal

Faol moddaning dozasi

30 mg

Aloqalar

Agar siz nojo'ya reaktsiya bo'lgan deb gumon qilsangiz, bu haqda shifokor yoki farmatsevtga xabar bering. Bu preparat uchun ko'rsatmalarda tavsiflanmagan har qanday mumkin bo'lgan noxush hodisalarga nisbatan qo'llaniladi

Shuningdek, dori vositalarni suiiste'mol qilish yoki noto'g'ri foydalanish, dozani oshirib yuborish yoki ishlatilgan dorilarning samarasizligi yoki dori vositalarning o'zaro ta'siri haqida shubhangiz bo'lsa, xabar bering.

Noxush hodisalar haqida xabar berish orqali siz preparatning xavfsizligi haqida ko'proq ma'lumot olishingiz mumkin.

Shuningdek, siz noxush hodisalar haqida to'g'ridan-to'g'ri Milliy nojo'ya reaktsiyalar haqida hisobot berish tizimiga xabar berishingiz mumkin. Oʻzbekiston Respublikasi Sogʻliqni saqlash vazirligi huzuridagi “Farmatsevtika mahsulotlari xavfsizligini taʼminlash markazi” davlat muassasasi E-mail: farmakonadzor@ssv.uz 100002, Toshkent sh., Ozod koʻchasi, K. Umarov tor koʻchasi, 16. +998 (71)203-01-01 (ichki raqam 2144).

Siz ushbu shakldan shubhali nojo'ya ta'sirlar va preparatning xavfsizligi bilan bog'liq boshqa ma'lumotlar haqida xabar berish uchun ham foydalanishingiz mumkin.

Hisobot bergan shaxs haqida ma'lumot

Shubhali nojo'ya reaktsiya haqida xabar berish
Mamlakat
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Bemor haqida ma'lumot

Noxush hodisalar paydo bo'lgan paytdagi yoshi (birlik)
  • Noxush hodisalar paydo bo'lgan paytdagi yoshi (birlik)
  • kunlar
  • haftalar
  • oylar
  • yillar
Yosh guruhi
  • Yosh guruhi
  • Homila
  • yangi tug'ilgan chaqaloq (0-27 kun)
  • chaqaloq (28 kun - 12 oy)
  • bolalar (1 yoshdan 12 yoshgacha)
  • o'smirlar (13-18 yosh)
  • kattalar (19-64 yosh)
  • keksalar (65 yosh va undan katta)
Jinsi

Noxush hodisalar

- None -
  • - None -
  • sekunda
  • daqiqalar
  • soatlar
  • kunlar
  • oylar
  • yillar
- Select -
  • - Select -
  • noma'lum
  • davolandi / yo'qoldi
  • davolanmoqda / yo'qolmoqda
  • davolab bo'lmaydi / yo'qolmadi
  • to'liq tiklanish / oqibatlarini bartaraf etish
  • halokatli natija

Noxush hodisani keltirib chiqarishda gumon qilingan preparat

- None -
  • - None -
  • noma'lum
  • qabul qilishni to’xtatdi
  • preparatning dozasi kamaytirildi
  • mahsulotning dozasi oshirildi
  • doza o'zgarmadi, bemor preparatni qo'llashda davom etmoqda
Bemor mahsulotdan takroriy foydalandimi?

Yevropa Parlamenti va Kengashning (EI) 2016/679 (“GDPR”) reglamentiga muvofiq, biz sizni ishontirib aytmoqchimizki, shubhali noxush hodisalarining aniq bir hodisasi bilan bog'liq holda bizga taqdim etgan barcha shaxsiy ma'lumotlar quyidagi manzilda konfidensial saqlanadi va PRO.MED.CS Praha a.s. (keyingi o'rinlarda nazoratchi deb yuritiladi) tomonidan nazoratchining standart ish tartib-qoidalariga muvofiq dori vositalari xavfsizligi va farmakovigilansiya qonunchiligiga rioya qilish uchun foydalaniladi.

Sizning shaxsiy ma'lumotlaringiz shubhali noxush hodisalarning aniq holatini to'g'ri boshqarish maqsadida foydalaniladi, bu ba'zi hollarda to'liq va aniq ma'lumotlarni to'plash va qayta ishlash uchun siz bilan samarali aloqada bo'lish zarurligini o'z ichiga oladi. Kelgusida sizning shaxsiy ma'lumotlaringiz tegishli me'yoriy majburiyatlarga rioya qilish uchun sog'liqni saqlash nazorat organlariga taqdim etilishi mumkin.

Shaxsiy ma'lumotlarni qayta ishlash bilan bog'liq holda, ushbu bildirishnomada ko'rsatilganidek, siz shaxsiy ma'lumotlarga kirish huquqi bilan boshqaruvchiga murojaat qilish, shaxsiy ma'lumotlarning nusxasini so'rash, ularga tuzatishlar kiritish, ularni o'chirish yoki qayta ishlashni cheklash va/yoki tegishli ma'lumotlarni himoya qilish nazorat organiga shikoyat qilish huquqiga egasiz.