[1] |
US FDA. Recalls of Angiotensin II Receptor Blockers (ARBs) including Valsartan, Losartan and Irbesartan [EB/OL]. [2021-02-03] https://www.fda.gov/drugs/drug-safety-and-availability/recalls-angiotensin-ii-receptor-blockers-arbs-including-valsartan-losartan-and-irbesartan
|
[2] |
EMA. CHMP List of outstanding issues to be addressed by the marketing authorisation holders for angiotensin-II receptor antagonists (sartans) containing a tetrazole group [EB/OL]. [2018-09-20] https://www.ema.europa.eu/en/documents/referral/angiotensin-ii-receptor-antagonists-sartans-article-31-referral-chmp-list-questions-be-addressed_en-0.pdf
|
[3] |
US FDA. Guidance for Industry: Control of Nitrosamine Impurities in Human Drugs [EB/OL]. [2021-02-01] https://www.fda.gov/media/141720/download
|
[4] |
EMA. European Medicines Regulatory Network approach for the implementation of the CHMP Opinion pursuant to Article 5(3) of Regulation (EC) No 726/2004 for nitrosamine impurities in human medicines [EB/OL]. [2021-02-22] https://www.ema.europa.eu/en/documents/referral/european-medicines-regulatory-network-approach-implementation-chmp-opinion-pursuant-article-53/2004-nitrosamine-impurities-human-medicines_en.pdf
|
[5] |
Center for Drug Evaluation, NMPA. Technical Guidelines for research on nitrosamine Impurities in Chemical Drug Products (Trial) [EB/OL]. [2020-05-08] https://www.cde.org.cn/main/news/viewInfoCommon/776b663787ec5a60ac744071c3714d5a
|
[6] |
US FDA. Information about Nitrosamine Impurities in Medications [EB/OL]. [2021-11-18] https://www.fda.gov/ drugs/drug-safety-and-availability/information-about-nitrosamine-impurities-medications
|
[7] |
EMA. Nitrosamine impurities [EB/OL]. [2022-04-30] https://www.ema.europa.eu/en/human-regulatory/post-authorisation/referral-procedures/nitrosamine-impurities# lessons-learned-with-sartan-medicines-and-recommendations-section
|
[8] |
EMA. Questions and answers for marketing authorisation holders/applicants on the CHMP Opinion for the Article 5(3) of Regulation (EC) No 726/2004 referral on nitrosamine impurities in human medicinal products [EB/OL]. [2022-05-20] https://www.ema.europa.eu/en/documents/referral/nitrosamines-emea-h-a53-1490-questions-answers-marketing-authorisation-holders/applicants-chmp-opinion-article-53-regulation-ec-no-726/2004-referral-nitrosamine-impurities-human-medicinal-products_en.pdf
|
[9] |
ICH. ASSESSMENT AND CONTROL OF DNA REACTIVE (MUTAGENIC) IMPURITIES IN PHARMACEUTICALS TO LIMIT POTENTIAL CARCINOGENIC RISK M7 (R1) [EB/OL]. [2017-03-31] https://database.ich.org/sites/default/files/M7_R1_Guideline.pdf
|
[10] |
US FDA. FDA Updates and Press Announcements on Angiotensin II Receptor Blocker (ARB) Recalls (Valsartan, Losartan, and Irbesartan) [EB/OL]. [2019-11-07] https://www.fda.gov/drugs/drug-safety-and-availability/fda-updates-and-press-announcements-angiotensin-ii-receptor-blocker-arb-recalls-valsartan-losartan
|
[11] |
US FDA. Search List of Recalled Angiotensin II Receptor Blockers (ARBs) including Valsartan, Losartan and Irbesartan [EB/OL]. [2021-10-20] https://www.fda.gov/drugs/drug-safety-and-availability/search-list-recalled-angiotensin-ii-receptor-blockers-arbs-including-valsartan-losartan-and
|
[12] |
EMA. Angiotensin-II-receptor antagonists (sartans) containing a tetrazole group [EB/OL]. [2022-05-20] https://www.ema.europa.eu/en/medicines/human/referrals/angiotensin-ii-receptor-antagonists-sartans-containing-tetrazole-group
|
[13] |
US FDA. FDA Updates and Press Announcements on NDMA in Metformin [EB/OL]. [2021-01-06] https://www.fda.gov/drugs/drug-safety-and-availability/fda-updates-and-press-announcements-ndma-metformin
|
[14] |
US FDA. Search list of recalled metformin products [EB/OL]. [2022-01-03] https://www.fda.gov/drugs/drug-safety-and-availability/search-list-recalled-metformin-products
|
[15] |
US FDA. FDA Updates and Press Announcements on NDMA in Zantac (ranitidine) [EB/OL]. [2020-04-16] https://www.fda.gov/drugs/drug-safety-and-availability/fda-updates-and-press-announcements-ndma-zantac-ranitidine
|
[16] |
EMA. Ranitidine-containing medicinal products [EB/OL]. [2022-05-20] https://www.ema.europa.eu/en/medicines/human/referrals/ranitidine-containing-medicinal-products
|
[17] |
US FDA. FDA Updates and Press Announcements on Nitrosamines in Rifampin and Rifapentine [EB/OL]. [2021-01-28] https://www.fda.gov/drugs/drug-safety-and-availability/fda-updates-and-press-announcements-nitrosamines-rifampin-and-rifapentine
|
[18] |
EMA. EMA update on metformin diabetes medicines [EB/OL]. [2019-12-06] https://www.ema.europa.eu/en/news/ema-update-metformin-diabetes-medicines
|
[19] |
US FDA. FDA Updates and Press Announcements on Nitrosamine in Varenicline (Chantix) [EB/OL]. [2022-05-05] https://www.fda.gov/drugs/drug-safety-and-availability/fda-updates-and-press-announcements-nitrosamine-varenicline-chantix
|
[20] |
EMA. Champix (varenicline) - lots to be recalled due to presence of impurity N-nitroso-varenicline above the Pfizer acceptable daily intake limit [EB/OL]. [2021-07-15] https://www.ema.europa.eu/en/documents/dhpc/direct-healthcare-professional-communication-dhpc-champix-varenicline-lots-be-recalled-due-presence_en.pdf
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