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Saturday, September 20, 2025
TopicFDA

Topic: FDA

Tariff cloud looming, US study links Indian generic drugs with 54% higher severe adverse events

Researchers associated with The Ohio State University found that number of severe adverse events linked to generic drugs made in India was 54% higher than for those made in the US.

Govt says no plan to ban heartburn drug ranitidine, carcinogenic impurities within safe limits

In 2019, evidence showed that an impurity in drug degrades over time to form probable carcinogenic compound. Ranitidine is sold as heartburn medicine under names Rantac, Aciloc & Zinetac.

1st US FDA-approved drug invented in India set for local launch as part of combination antibiotic

Combination of enmetazobactam, invented by scientists associated with Chennai-based pharma firm Orchid Pharma in 2008, and antibiotic cefipime is used to treat severe bacterial infection.

‘Ban McDonald’s nationwide,’ says traders’ body after ‘fake cheese’ found in burger in Maharashtra

Such fraudulent practices cannot be tolerated, CAIT adds. This comes after Food & Drug Administration allegedly found counterfeit cheese at fast food giant's outlet in Ahmednagar.

US cracks down on healthcare product makers following cough syrup deaths overseas

Cough syrups made in India & Indonesia have been linked to deaths of over 300 children globally. Medicines were found to contain high levels of DEG, EG, leading to death.

Op Broader Sword: India, US join hands to crack down on shipments of ‘illicit’ drugs, medical devices

Operation targeted packages entering US from India through New York (JFK) & Chicago (ORD) International Mail Facilities (IMFs) last month. Over 500 shipments seized, Indian national held.

After Singapore, US now approves sale of lab-grown meat in restaurants, grocery stores

The US government’s approval to two California-based companies is being seen as a huge step for the alternative protein industry.

US FDA asks India’s Sun Pharma to halt trials on experimental dermatological drug

Sun Pharma said FDA has also stated that patients with alopecia areata on 12 mg dose of the drug deuruxolitinib should discontinue its use, Sun Pharma said.

US FDA takes new dengue vaccine by Japanese firm Takeda for priority review

Takeda has carried out phase 3 trials of the vaccine candidate and found it to be 80.2% effective in preventing symptomatic dengue cases after a year of vaccination.

‘No prescription sought, drugs under different names’ — Maharashtra FDA busts ‘abortion pill racket’

FDA officers in 13 parts of the state posed as customers and managed to easily procure the kits. FIRs lodged against e-commerce app, ‘unlicensed’ agency.

On Camera

Was India’s public sector born out of European envy?

For all its obvious blemishes, capitalism alone holds out the most creative and dynamic force that any civilization has ever discovered, wrote BP Godrej in 1980.

Market regulator SEBI clears Adani Group of impropriety alleged by Hindenburg Research

SEBI probe concluded that purported loans and fund transfers were paid back in full and did not amount to deceptive market practices or unreported related party transactions.

2 Assam Rifles personnel killed as convoy ambushed in Manipur, on ‘same route Modi took’ fortnight ago

This is the first major attack on central security forces since last November, when a CRPF jawan was killed and four were injured in an ambush in Jiribam on Manipur-Assam border. 

India doesn’t give walkovers to Pakistan in war. Here’s why it shouldn’t do it in cricket either

Many really smart people now share the position that playing cricket with Pakistan is politically, strategically and morally wrong. It is just a poor appreciation of competitive sport.