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2020.10.7 Acetaminophen Toxicity: A History of Serendipity and Unintended Consequences William M. Lee M.D., F.A.C.P., F.A.A.S.L.D. ... an editorial in Lancet in 1975, 45 years ago, opined: ¡§Surely it is time to replace paracetamol with an effective analogue which cannot cause liver damage. 45¦~«eªº1975¦~¡A¬h¸¤M¤Wªº¤@½gªÀ½×«ü¥X¡G¡§²{¦b¬O®ÉԥΤ@ºØ¤£·|¤Þ°_¨x·l¶Ëªº¦³®ÄÃþ¦üª«¥N´À¼³¼ö®§µh¡C aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.984
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-------------------------------------------------------------------------------------------- ·|û¡G¾¾¹À©OÎN¹À«¡10150521 µoªí®É¶¡:2021/1/27 ¤U¤È 10:13:44²Ä 607 ½g¦^À³ ®Ú¾ÚIMS Health ²Îp¸ê®ÆÅã¥Ü¥þ¬üAcetaminophen ÃÄ«~¥«³õ¾P°âÃB¦Û 2015 ªº 35.6 »õ¡A ³v¦~¤U°¦Ü 2018 ªº 22.2 »õ
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www.federalregister.gov/documents/2018/12/11/2018-26712/list-of-drug-products-that-have-been-withdrawn-or-removed-from-the-market-for-reasons-of-safety-or ---------------------------------------------------------------------------------------- III. Proposed Rule and Final Rule A. Presentation to the Advisory Committee At a meeting held on June 17 and 18, 2015 (see the Federal Register of May 22, 2015 (80 FR 29717)), FDA presented to the Committee FDA¡¦s proposal to add to the withdrawn or removed list all drug products containing more than 325 mg of acetaminophen per dosage unit, all drug products containing aprotinin, all drug products containing bromocriptine mesylate for the prevention of physiological lactation, and all intravenous drug products containing greater than a 16 mg single dose of ondansetron hydrochloride. The Committee voted in favor of including each drug product entry on the list as proposed by FDA.[1]
B. The Proposed Rule In the Federal Register of October 18, 2016, FDA proposed to revise the withdrawn or removed list to add all drug products containing aprotinin, all drug products containing bromocriptine mesylate for the prevention of physiological lactation, and all intravenous drug products containing greater than a 16 mg single dose of ondansetron hydrochloride (October 2016 proposed rule). The addition of all drug products containing more than 325 mg of acetaminophen per dosage unit to the list was not included in the October 2016 proposed rule and remains under consideration by the Agency.
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Bromocriptine mesylate»POndansetron hydrochloride ³o2¤ä¥X©ó¦w¥þ©Î¦³®Ä©Êªº¦Ò¼{¡A ³QFDAºM¦^©ÎºM¥X¥«³õ¡C
¦Ü©óAPAP¦p¤U¡A¬Ý¤£À´¨SÃö«Y¡A¤Ï¥¿¥X²{¦bº]¤Wªº´N¤£¬O¦n¨Æ±¡!¤§«áµo®i´N¬Ý¤U¥h... The addition of all drug products containing more than 325 mg of acetaminophen per dosage unit to the list was not included in the October 2016 proposed rule and remains under consideration by the Agency. |
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--------------------------------------------------------------------------------------- NEIL KAPLOWITZ, M.D. Keck School of Medicine University of Southern California Los Angeles, CA
Should the FDA withdraw APAP from the market? Given what we know about the nonsuicidal chronic overdosing leading to acute liver failure, this is a valid question. Unfortunately the alternative, nonsteroidal antiinflammatory drugs, have their own inherent problems unrelated to liver failure, such as ulcers, gastrointestinal bleeding, and renal damage.So we¡¦re left with a ¡§pick your poison¡¨ dilemma until a safer analgesic/antipyretic is available. .....the next step, in my opinion, is to eliminate acetaminophen from all combinations, including over-the-counter preparations and opiates --------------------------------------------------------------------------------------------
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