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Compounded Versions Of Weight Loss And Diabetes Drugs Led To Death And Hospitalization, Novo Nordisk Says It Is Aware

Compounded Versions Of Weight Loss And Diabetes Drugs Led To Death And Hospitalization, Novo Nordisk Says It Is Aware

諾和諾德表示,混合版本的減肥和糖尿病藥物導致死亡和住院,該公司已經意識到這一情況。
Benzinga ·  11/07 23:13

Earlier, Novo Nordisk A/S (NYSE:NVO) petitioned the FDA to ban compounding pharmacies from producing cheaper, unapproved versions of its drugs Wegovy and Ozempic.

此前,諾和諾德公司(Novo Nordisk A/S,紐交所代碼:NVO)向FDA提出申請,要求禁止配製藥店生產其藥物Wegovy和Ozempic的價格更便宜、未經批准的版本。

Amid shortages and rising demand for branded drugs, compounded semaglutide has gained popularity due to its affordability.

在品牌藥物短缺和需求上升的情況下,由於價格實惠,混合塞麥格列汀變得受歡迎。

However, Novo Nordisk contends that only FDA-approved versions should be available, emphasizing the safety risks associated with compounded drugs.

然而,Novo Nordisk 認爲只有經 FDA 批准的版本應該可用,強調了混合藥物帶來的安全風險。

Novo Nordisk's Chief Financial Officer Karsten Munk Knudsen has reportedly confirmed that the company was aware of at least ten deaths and 100 hospitalizations linked to these compounded versions of semaglutide-based drugs.

諾和諾德的致富金融官Karsten Munk Knudsen據報道確認,公司已注意到至少有十人死亡和100人住院,與這些複方版的賽格魯肽類藥物有關。

Also Read: Eli Lilly Sues Some Vendors For Unauthorized Sale Of Fake Weight-Loss Drug

另請參閱:禮來起訴一些供應商未經授權銷售假減肥藥。

However, he noted that no definitive cause of death is identified in the reports, as the data is pulled from the FDA adverse events database.

然而,他指出報告中未明確確定死因,因爲數據來自FDA不良事件數據庫。

Last week, the update came as the FDA revised its shortage list to note that the .25 mg starter dose of semaglutide-based obesity med Wegovy is now available in the U.S.

上週,FDA更新了短缺清單,指出基於賽格魯肽的肥胖藥物Wegovy的0.25毫克起始劑量現在在美國可獲得。

Less than a month ago, the FDA removed Eli Lilly And Co's (NYSE:LLY) tirzepatide from its shortage list.

不到一個月前,FDA將禮來公司(NYSE:LLY)的替替唑胰酮從短缺清單中移除。

Soon after the shortage was resolved, the FDA reminded compounders of the legal restrictions on making copies of FDA-approved drugs. The update has sparked concern among medical professionals, patients, and drug compounding facilities.

短缺問題解決後不久,FDA提醒混合劑製造商遵守法律限制,不得複製FDA批准的藥物。此更新引起醫療專業人士、患者和藥物混合設施的關注。

A company spokesperson referred Reuters to the FDA's database, which tracked these events over the past two years. Adverse event reports, which are submitted by doctors, patients, drugmakers, and others, are primarily used as an early warning system.

一位公司發言人轉介路透社至FDA數據庫,追蹤過去兩年內的這些事件。由醫生、患者、藥品製造商和其他人提交的不良事件報告主要用作早期預警系統。

These reports are not considered conclusive evidence of causality and often lack important details. Furthermore, it is possible that multiple submissions may describe the same incident.

這些報告並非可靠的因果關係證據,並常常缺乏重要細節。此外,可能會有多份提交描述同一事件。

Knudsen also discussed the company's ongoing efforts to address safety concerns related to compounded versions of its drugs.

Knudsen還討論了公司持續努力解決與其藥物復配版本相關的安全問題。

He mentioned that Novo Nordisk has been monitoring the market for compounded products and has identified several safety issues.

他提到Novo Nordisk一直在監測混合產品市場,已確定幾個安全問題。

Novo Nordisk argues that these compounded versions may pose safety risks, such as impurities and incorrect dosages, and sometimes lack the active ingredient entirely.

Novo Nordisk 認爲這些混合版本可能存在安全風險,如雜質和劑量不正確,有時完全缺乏有效成分。

On Wednesday, Novo Nordisk released Q3 earnings. "Following higher-than-expected volume growth in recent years, including GLP-1-based products such as Ozempic and Wegovy, combined with the expectation of continued volume growth and capacity limitations at some manufacturing sites, the outlook also reflects expected continued periodic supply constraints and related drug shortage notifications across a number of products and geographies," it added.

週三,Novo Nordisk發佈了第三季度收益報告。"包括Ozempic和Wegovy等基於GLP-1的產品近年來的成交量增長高於預期,再加上預計持續的成交量增長和一些製造地點的產能限制,前景也反映了預期持續的偶發供應約束及涉及多款產品和地理位置的藥物短缺通知," 其補充道。

Price Action: NVO stock is up 1.59% at $107.04 at the last check on Thursday.

股價行情:NVO股價在週四最後一次檢查時上漲1.59%,報107.04美元。

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譯文內容由第三人軟體翻譯。


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