GMPc Vietnam JSC
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Thực phẩm chức năng chứa chất kích dục tương tự Viagra bị thu hồi

06/09/2016 | 1557 | Tin tức Tổng hợp

Cục An toàn thực phẩm, Bộ Y tế vừa ra quyết định thu hồi sản phẩm Avena plus vì chứa chất sildenafil, một loại tân dược bị cấm sử dụng trong thực phẩm chức năng.
 
Đây là sản phẩm của Công ty Đầu tư và Thương mại xuất nhập khẩu Việt Nam Canoves ( Hà Nội). Thực phẩm bảo vệ sức khỏe Avena bị thu hồi có số lô 010316, ngày sản xuất 2/3/2016, hạn sử dụng 1/3/2019. 
 
 
Kết quả kiểm nghiệm mẫu của Viện Kiểm nghiệm an toàn vệ sinh thực phẩm quốc gia cho thấy sản phẩm có chứa chất cấm sildenafil. Vì thế, Cục An toàn thực phẩm yêu cầu tạm dừng lưu thông sản phẩm có số lô trên. Công ty có trách nhiệm thực hiện các biện pháp xử lý, thu hồi trong thời hạn 10 ngày và gửi báo cáo về Cục.
 
Cục cũng yêu cầu công ty cung cấp thông tin liên quan đối với lô hàng không đạt bao gồm: số lượng hàng hóa cùng lô đã sản xuất, lưu thông, tồn kho và thu hồi tính đến ngày gửi báo cáo.
 
Sildenafil là một hoạt chất của Viagra, loại tân dược được dùng để điều trị yếu sinh lý, rối loạn cương dương. Là thuốc trị bệnh nên nó được sử dụng theo đơn của bác sĩ, với liều lượng, hàm lượng nhất định. Sildenafil được một số nhà sản xuất cho vào thành phần các thực phẩm chức năng được quảng cáo bổ thận tráng dương dù bị cấm.
 
Mới đây, cơ quan chức năng phát hiện hoạt chất vardenafil, một tân dược bị cấm sử dụng trong các loại thực phẩm chức năng. Đây là một hoạt chất tương tự Viagra được xếp vào nhóm chất kích dục, cũng được chỉ định điều trị rối loạn cương dương. Nếu sử dụng quá liều vardenafil sẽ vô cùng nguy hại, nhất là người bệnh tim mạch, có nguy cơ làm tăng nhịp tim, tăng lượng máu đến các cơ quan khác.

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  • GMPc Vietnam JSC
  • Head Office: No. 18, Mang Cam 1 Street, An Lac Green Symphony, Van Canh Ward, Hoai Duc District, Hanoi City
  • Business location : No. 32, Vi Cam 5 Street, An Lac Green Symphony, Van Canh Ward, Hoai Duc District, Hanoi City
  • Tel: 0243.787.2242 | CEO hotline: 0982.866.668
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  • Home
  • About Us
    • Summary information
    • Key Personnel
  • Services
    • WHO GMP Pharmaceutical facilities
      • Project feasibility study
      • Technology and Equipment consultation
      • Detail Construction and MEP drawing
      • Project Management and Supervision
      • WHO GMP Training and Guidance
      • Preparation of WHO GMP registration dossier
      • WHO GMP Re-evaluation consultation
    • EU GMP Pharmaceutical Factory
      • Feasibility study report
      • Design detailed construction drawings
      • QM documentation – Validation
      • GMP application and product dossier application
      • Project management - Construction supervision
    • CGMP, ISO 22716-certified cosmetics facilities
      • Project feasibility study
      • Technology and Equipment consultation
      • Detail Construction and MEP drawing
      • Project Management and Supervision
      • CGMP ASEAN Training and Guidance
      • Preparation of CGMP ASEAN/ ISO 22716 registration dossier
      • CGMP ASEAN Re-evaluation consultation
    • Health-supplement facilities
      • Project feasibility study
      • Technology and Equipment consultation
      • Detail Construction and MEP drawing
      • Project Management and Supervision
      • HS GMP Training and Guidance
      • Preparation HS GMP registration dossier
      • HS GMP - Re-evaluation consultation
    • Eligibility For Cosmetic Manufacturing
      • Overall consultation
      • Detail Construction and MEP drawing
      • Designing, Constructing, Ensured Certification
      • Preparation of Registration Dossier
    • Pharmaceutical distribution center
      • Feasibility Study
      • Design and Information Technology Solutions
      • Project Management and Supervision
      • GSP registration and operation consultancy
    • GSP warehouses
      • Project feasibility study
      • Detail Construction and MEP drawing
      • GSP Training and Guidance
      • Overall Consultation on Designing And Constructing
      • GSP Re-evaluation consultation
    • Veterinary Pharmaceutical Facilities
      • Project Feasibility Study
      • Technology and Equipment consultation
      • Detail Construction and MEP Drawing
      • Project management and Supervision
      • WHO GMP Training and Guidance
      • Preparation of WHO GMP registration dossier
      • WHO GMP Re-evaluation consultation
    • GMP, GLP, GSP training
      • Basis knowledge
      • Intensive Training
    • Other GPs’s consultation
      • GLP inspection laboratories
      • GDP distribution systems
      • GPP pharmacy
      • WHO GACP medicinal materials
    • Register and Announce
      • Announcement of Imported Cosmetic
    • Dairy Factory
      • Overall Planning
      • Detailed Construction & MEP Design - Project Budgeting
      • Contractor/Supplier Consultation and Project Management
      • Training, Drafting registration dossier
  • Project
  • Video
  • GMP-Handbook
  • Faqs
  • News
  • Jobs
  • Contact
 
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