World

Dostarlimab: A wonder new drug ? KOCHI: The name Dostarlimab, unheard of till recently, has become a household name...

The U.S. Food and Drug Administration (USFDA) has approved a supplemental indication for Qsymia (phentermine and topiramate extended-release capsules) for chronic weight management in...

Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Propofol Injectable Emulsion, USP (containing benzyl alcohol), 100 mL Single Patient...

FAQS on Monkeypox by WHO Q. What is monkeypox? Ans: Monkeypox is an illness...

First eye drop approved that can eliminate the need for reading glasses As a kid, you would have...

Washington: Amid the US Supreme Court's decision to ban abortion in the country, the Food and Drug Administration (USFDA) is considering approving the...

Mylan Pharmaceuticals Inc., a Viatris company, is voluntarily recalling one batch of Insulin Glargine (Insulin glargine-yfgn) Injection, 100 units/mL (U-100), 3 mL...

New Omicron subvariant BA.2.75 WHO explains severity The detection of the new Omicron...

New York: The U.S. Food and Drug Administration (USFDA) said it has authorized state-licensed pharmacists to prescribe Pfizer Inc's COVID-19 pill to eligible patients...

Researchers from Rice University and the University of Texas MD Anderson Cancer Center have discovered potential new drugs that work in concert...

Burbank, California, Bryant Ranch Prepack Inc. is voluntarily recalling one lot of Morphine Sulfate 30 mg Extended-Release tablets (comprised of 10 bottles),...

LiveMetric, a leader in medical wearable technology, announced the launch of LiveOne, the world’s first 510(k) US Food and Drug Administration (USFDA)...

In a bid to increase its efforts towards recognition and acceptance of IP in foreign countries, the Indian Pharmacopoeia Commission (IPC) has...

The Central government is in talks with the United Arab Emirates (UAE) to include Indian Pharmacopoeia (IP) in the standards of pharmaceuticals...

Blood Bank / Centre: Difference Between SDP and RDP The key difference between SDP and RDP is that SDP is a...

The U.S. Food and Drug Administration (USFDA) has approved a supplemental indication for Imcivree (setmelanotide) injection for chronic weight management in adult and...

The UK is set to play a greater international role in making sure medicines and medical devices are regulated safely and efficiently...

Concerned over the rise of infectious diseases which cover the coronavirus disease and tuberculosis among others, the USFDA has issued draft norms...

For many decades, aspirin was advised to prevent heart attacks, both for those who had pre-existing cardiovascular disease (CVD) and to prevent...

New Haven , June 1 (ANI): According to a new study, common painkillers can have unexpected and unexplained impacts on numerous conditions,...

Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for the Volara System (home care) to reinforce important safety information...

The U.S. Food and Drug Administration (USFDA) said it has withdrawn its approval for TG Therapeutics Inc's lymphatic cancer treatment Ukoniq over concerns of higher risk of...

The US Food and Drug Administration (USFDA), which had put on hold the phase-II/III clinical trials of Bharat Biotech’s C-19 vaccine Covaxin,...

In a big relief for Indian drug manufacturers and exporters engaged in unprofessional act in connivance with Nigerian importers, the National Agency...