副作用は、医薬品医療機器法第68条の10第2項に従って厚生労働大臣に報告する必要があります。医療機関から厚生労働大臣に直接報告する場合は、PMDAのホームページ をご参照ください。
ムンディファーマの製品による副作用情報は、弊社医薬情報担当者またはお客様相談窓口を介してご報告いただくことも可能です
お客様相談窓口: 0120-525-272
受付時間: 9:00~17:30(土日祝日、会社休日を除く)
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Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard
Adverse events should also be reported to Napp Pharmaceuticals Limited on 01223 424444 or drugsafetyUKandROI@mundipharma.com
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For General Public: Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Napp Pharmaceuticals Limited at drugsafetyUKandROI@mundipharma.com.
For Healthcare Professionals: If you get any side-effects, talk to your doctor, nurse or pharmacist. This includes any possible side-effects not listed in the package leaflet. You can also report side-effects directly via the Yellow Card scheme at www.mhra.gov.uk/yellowcard. By reporting side-effects you can help provide more information on the safety of this medicine.
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