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Eye Condition a ‘Very Rare’ Side Effect of Semaglutide, EMA Says

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Eye Condition a ‘Very Rare’ Side Effect of Semaglutide, EMA Says

June 06, 2025

FDA Drops REMS Requirement for Antihypertensive Aprocitentan

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FDA Drops REMS Requirement for Antihypertensive Aprocitentan

Michael O'Riordan

April 09, 2025

EMA: No Evidence of Link Between GLP-1 Receptor Agonists and Suicidal Thoughts

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EMA: No Evidence of Link Between GLP-1 Receptor Agonists and Suicidal Thoughts

April 12, 2024

FDA: No Signs of Link Between GLP-1s and Suicidal Thoughts, Actions

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FDA: No Signs of Link Between GLP-1s and Suicidal Thoughts, Actions

January 12, 2024

Asundexian’s Lack of Efficacy Sinks OCEANIC-AF

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Asundexian’s Lack of Efficacy Sinks OCEANIC-AF

November 20, 2023

GLP-1 Meds Linked to 265 Reports to FDA of Suicidal Ideation: Reuters

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GLP-1 Meds Linked to 265 Reports to FDA of Suicidal Ideation: Reuters

September 28, 2023

‘Overwhelming Reduction’ in Bleeding With Abelacimab vs Rivaroxaban in AF

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‘Overwhelming Reduction’ in Bleeding With Abelacimab vs Rivaroxaban in AF

September 18, 2023

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

A Simple Nudge Moves the Needle on Statin Prescribing

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A Simple Nudge Moves the Needle on Statin Prescribing

Michael O'Riordan

December 02, 2022

DELIVER Trial Scores a Win for Dapagliflozin in HFpEF

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DELIVER Trial Scores a Win for Dapagliflozin in HFpEF

May 05, 2022

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

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Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

August 20, 2021

FDA: Obesity Drug Lorcaserin Exits US Market Over Cancer Concerns

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FDA: Obesity Drug Lorcaserin Exits US Market Over Cancer Concerns

February 14, 2020

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

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FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

Michael O'Riordan

November 14, 2019

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

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FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

Michael O'Riordan

May 08, 2019

TCTMD’s Top 10 Most Popular Stories for April 2019

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TCTMD’s Top 10 Most Popular Stories for April 2019

May 01, 2019

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

FDA Adds Boxed Warning About CV Risks to Gout Drug Febuxostat

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FDA Adds Boxed Warning About CV Risks to Gout Drug Febuxostat

February 22, 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 Warns of Stroke and Arterial Dissection Risk With MS Drug

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FDA Warns of Stroke and Arterial Dissection Risk With MS Drug

November 29, 2018

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