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FDA Drops REMS Requirement for Antihypertensive Aprocitentan

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FDA Drops REMS Requirement for Antihypertensive Aprocitentan

Michael O'Riordan

April 09, 2025

Abiomed Recalls Labeling for Left-Sided Impella Pumps: FDA

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Abiomed Recalls Labeling for Left-Sided Impella Pumps: FDA

March 21, 2024

European Regulators Investigating CV Safety of Weight-Loss Drug Mysimba

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European Regulators Investigating CV Safety of Weight-Loss Drug Mysimba

Michael O'Riordan

September 15, 2023

Generic Dabigatran Lots Pulled for Nitrosamine Impurity

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Generic Dabigatran Lots Pulled for Nitrosamine Impurity

Michael O'Riordan

March 28, 2023

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

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Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

August 20, 2021

FDA: Some Tainted Losartan Must Remain on US Market to Maintain Adequate Access for Patients

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FDA: Some Tainted Losartan Must Remain on US Market to Maintain Adequate Access for Patients

March 21, 2019

FDA Provides Update on Tainted ARB Investigation, With New Impurity Found

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FDA Provides Update on Tainted ARB Investigation, With New Impurity Found

March 04, 2019

More Blood-Pressure Drugs Recalled Due to Cancer-Causing Impurities

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More Blood-Pressure Drugs Recalled Due to Cancer-Causing Impurities

December 10, 2018

FDA: Contaminated Irbesartan Now Under Voluntary Recall

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FDA: Contaminated Irbesartan Now Under Voluntary Recall

Michael O'Riordan

October 31, 2018

FDA Recalls Valsartan-Containing Drugs After Detection of Carcinogen

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FDA Recalls Valsartan-Containing Drugs After Detection of Carcinogen

Michael O'Riordan

July 16, 2018

News Daily News

Experimental FAAH Inhibitors Do Not Pose Safety Risk, FDA Concludes

Michael O'Riordan

August 12, 2016

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