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Charting India's Pharmaceutical Future at the 74th IPC - Pharmacy Infoline 15/08/2025

Charting India's Pharmaceutical Future at the 74th Indian Pharmaceutical Congress : Dr. Milind Umekar

Charting India's Pharmaceutical Future at the 74th IPC - Pharmacy Infoline 74th Indian Pharmaceutical Congress (IPC), hosted in Bengaluru by Association of Pharmaceutical Teachers of India (APTI) and the Indian Pharmaceutical Congress Association (IPCA), Maha-Kumbh" of Indian Pharmacy

Jupiter Foundation Launches ‘My Organ Project’ to Promote Life-Saving Organ Donation Awareness - Pharmacy Infoline 11/12/2024

Jupiter Foundation’s ‘My Organ Project’ raises awareness about organ donation, dispels myths, and encourages pledging organs to save lives, fostering a culture of giving in India



Jupiter Foundation Launches ‘My Organ Project’ to Promote Life-Saving Organ Donation Awareness - Pharmacy Infoline Jupiter Foundation’s ‘My Organ Project’ raises awareness about organ donation, dispels myths, and encourages pledging organs to save lives, fostering a culture of giving in India

FDA Recalls Duloxetine Antidepressant: Carcinogenic Impurities Found in 233,000+ Bottles - Pharmacy Infoline 11/12/2024

FDA Recalls Duloxetine Antidepressant: Carcinogenic Impurities Found in 233,000+ Bottles
The U.S. Food and Drug Administration (FDA) has issued an urgent recall of over 233,003 bottles of duloxetine, a widely prescribed antidepressant, due to the detection of carcinogenic impurities. The recall, announced on November 19, 2024, highlights the presence of N-nitroso-duloxetine, a nitrosamine impurity exceeding the recommended safety limits.

FDA Recalls Duloxetine Antidepressant: Carcinogenic Impurities Found in 233,000+ Bottles - Pharmacy Infoline Rising Pharmaceuticals recalls over 233,000 bottles of duloxetine after FDA finds carcinogenic impurity N-nitroso-duloxetine above safe limits. Learn more about risks and alternatives.

Merck Announces Success of KEYLYNK-001 Trial in Ovarian Cancer Treatment - Pharmacy Infoline 11/12/2024

Merck Announces Success of KEYLYNK-001 Trial in Ovarian Cancer Treatment



Merck, known as MSD outside the U.S. and Canada, has achieved a major milestone in cancer research. The pharmaceutical giant announced that its phase 3 KEYLYNK-001 trial has met the primary endpoint of progression-free survival (PFS) for patients with BRCA non-mutated advanced epithelial ovarian cancer. This breakthrough highlights the potential of combining Keytruda (pembrolizumab) and Lynparza (olaparib), with or without bevacizumab, as a first-line treatment.

Merck Announces Success of KEYLYNK-001 Trial in Ovarian Cancer Treatment - Pharmacy Infoline Merck’s KEYLYNK-001 trial demonstrates significant improvement in progression-free survival (PFS) for BRCA non-mutated advanced ovarian cancer using Keytruda and Lynparza. Explore findings and implications

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