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FDA Requests Removal of Suicidal Ideation Warning From GLP-1 Labels

FDA Requests Removal of Suicidal Ideation Warning From GLP-1 Labels

by Admin | Mar 23, 2026 | News

FDA says it is requesting that drug application holders remove information regarding suicidal ideation and behavior from the labeling of certain GLP-1 receptor agonist medications, specifically Saxenda, Wegovy, and Zepbound. The agency says this follows a...
FDA Requires Vitamin B6 Deficiency Warning for Carbidopa/Levodopa

FDA Requires Vitamin B6 Deficiency Warning for Carbidopa/Levodopa

by Admin | Mar 22, 2026 | News

FDA says it is requiring application holders for all drug products containing carbidopa/levodopa to add a warning that these medicines can cause vitamin B6 deficiency and vitamin B6 deficiency-associated seizures. The agency says the products are approved to treat...
Industry Alert: Rising Scrutiny Over Proxy Interviews, False Representation, and Intermediary Misconduct in Pharmacovigilance Hiring

Industry Alert: Rising Scrutiny Over Proxy Interviews, False Representation, and Intermediary Misconduct in Pharmacovigilance Hiring

by Admin | Mar 18, 2026 | Careers, News

A growing wave of concern is emerging across parts of the pharmaceutical and drug safety industry over alleged proxy interviews, false professional representation, and unethical third-party involvement in pharmacovigilance hiring. Across regulated safety functions,...
MHRA Announces Bayer Recall Over Impurity Above Acceptable Limit

MHRA Announces Bayer Recall Over Impurity Above Acceptable Limit

by Admin | Mar 14, 2026 | News

MHRA has published a Class 3 Medicines Recall for Bayer Plc, various products, EL(26)A/12. The agency said Bayer is recalling all stock of the listed products as a precautionary measure because an impurity above the acceptable limit was identified. MHRA said the...
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