Lupin receives three USFDA observations for Aurangabad facility Farhat Nasim16 May 2019 9:45 AM ISTThe US Food and Drug Administration (USFDA) carried out the inspection at the plant from May 6 to May 15, Lupin said in a statement.Mumbai: Drug maker...
Sun pharma, Dr Reddys, others deny allegations of price fixing in US Garima16 May 2019 9:35 AM ISTIn separate clarifications to stock exchanges, the companies including Glenmark, Sun Pharma, Dr Reddy's, Aurobindo Pharma denied the accusations and...
JnJ to submit applications for at least 10 new drugs by 2023 Medical Dialogues Bureau16 May 2019 9:15 AM ISTThis is part of the healthcare conglomerate’s plan to deliver above-market growth through 2023 at its Janssen unit, JnJ said.New Delhi: Johnson &...
Students appeal to PM to enforce ban on e-cigarettes Medical Dialogues Bureau16 May 2019 9:00 AM IST"Students as young as 13 are using e-cigarettes as a fun device and later on getting addicted to it."New Delhi: Over 1000 students and teachers along...
Lupin gets 4 USFDA observations after closure of pharmacovigilance inspection Farhat Nasim15 May 2019 9:45 AM ISTThe inspection was conducted at its global pharmacovigilance group DSRM (Drug Safety & Risk Management) based out of Mumbai between January 14-18,...
Mifeprex sale via mail in US; lawmakers urge USFDA to crackdown on firms Medical Dialogues Bureau15 May 2019 9:40 AM ISTMifeprex is an oral drug that blocks the progesterone hormone necessary for a pregnancy to continue. It is used with Misprostol to end early...
Improper storage kills shelf life of drugs; Health Ministry raises concern Meghna A Singhania15 May 2019 9:31 AM ISTAs on April 2018, the total sanctioned strength of drug inspectors in the states and Union Territories is about 1,600, out of which about 1,200 drug...
Japan: Novartis gets Government nod for cancer treatment Kymriah at cost of $305800 Garima15 May 2019 9:15 AM ISTKymriah works by removing disease-fighting T-cells from individual patients, modifying them to attack cancer, and then re-infusing them back into the...
USFDA panel votes against Daiichi Sankyo blood cancer treatment Quizartinib Medical Dialogues Bureau15 May 2019 9:00 AM ISTThe panel voted 8-3 against the drug, quizartinib, after assessing data presented by the Japanese company.U.S: Independent experts on an advisory...
Glenmark Pharma gets USFDA nod for generic version of Nexium to treat acid reflux Farhat Nasim14 May 2019 10:30 AM ISTThe approved products Esomeprazole Magnesium delayed-release capsule is a generic version of AstraZeneca Pharmaceuticals' Nexium delayed-release...
Novartis recalls three lots of Promacta due to potential peanut contamination Farhat Nasim14 May 2019 10:00 AM ISTNew Delhi: Novartis recently announced a voluntary recall of three lots of Promacta (eltrombopag) 12.5 mg for oral suspension to the consumer level....
Eli Lilly gets USFDA nod for Cyramza to treat hepatocellular carcinoma Medical Dialogues Bureau14 May 2019 9:47 AM ISTThe USFDA has removed the boxed warning from the CYRAMZA labelling which highlighted warnings pertaining to haemorrhage, gastrointestinal perforation...
