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Cough Syrup
Two flats in Chennai belonging to the promoter of Sresan Pharmaceuticals, the manufacturer of Coldrif cough syrup linked to the death of at least 20 children in Madhya Pradesh, have been attached under the anti-money laundering law, the Enforcement Directorate said on Wednesday. The assets, located at Kodambakkam in Tamil Nadu's capital city, are owned by G Ranganathan and his family members, it said in a statement. The value of the flats is Rs 2.04 crore, the statement said. Ranganathan was arrested by Madhya Pradesh Police in October. The agency alleged Sresan Pharma indulged in "rampant unfair trade practices to suppress its manufacturing costs and increase profits which are nothing but proceeds of crime (under the Prevention of Money Laundering Act)." Probe found that the manufacturer used industry-grade raw materials in the manufacturing of medicines instead of pharma-grade raw materials "without" proper quality checks. "Such materials were being purchased in cash without ..
The Uttar Pradesh Special Task Force arrested a man from Lucknow on Tuesday in connection with illegal storage and trade of banned cough syrup and other drugs containing codeine, police said. According to a statement issued by the office of the Director General of Police, the Special Task Force (STF) had been receiving information about the illegal storage and trade of Phensedyl cough syrup and other drugs containing codeine for use as intoxicants. The informants revealed that these drugs were being sent to other parts of Uttar Pradesh, Uttarakhand, Bihar, Jharkhand, Assam, West Bengal and Bangladesh. Following this, the STF and the Food Safety and Pharmaceuticals Department formed a joint investigation committee, which subsequently recovered a large quantity of illicit Phensedyl cough syrup. A case was registered at Sushant Golf City police station following this. During investigation, the STF arrested two accused, Vibhor Rana and Vishal Singh, on November 12. Another accused, Am
A case has been registered against 28 drug dealers, including a father-son duo, in Varanasi for allegedly smuggling codeine-laced cough syrup for intoxication, police said on Monday. They said that an investigation by the Food Safety and Drug Administration Department revealed that Shubham Jaiswal, a resident of Prahlad Ghat, Varanasi, and his father, Bholanath Prasad, supplied large quantities of the banned adulterated syrup to 26 Varanasi-based businessmen from their Ranchi-based firm, Shaili Traders. Subsequently, a case was registered on Saturday based on a complaint lodged by Drug Inspector Junab Ali in Varanasi, police said. In the complaint, the drug inspector mentioned that, following the discovery that Shaili Traders had been selling large quantities of codeine-laced cough syrup in various districts of Uttar Pradesh, including Varanasi, the 26 Varanasi-based firms were inspected, and several were found to be closed. Calls to the numbers available on the firms' portals were
Haryana Health Minister Arti Singh Rao on Saturday said the government has issued a public health alert following the detection of diethylene glycol (DEG) impurity above permissible limits in a cough syrup formulation. The alert has been issued on the basis of an official communication received from the Central Drugs Standard Control Organisation's (CDSCO) sub-zonal office in Guwahati by the Food and Drugs Administration (FDA), Haryana. In an official statement, the minister informed that the cough syrup formulation -- "Planokuf D" syrup containing cetirizine hydrochloride, phenylephrine hydrochloride and dextromethorphan hydrobromide, and manufactured by Shreya Lifesciences Private Limited -- has been found to contain DEG impurity beyond permissible limits. The affected batch, bearing number R25053101, was manufactured in February and is set to expire in January 2027. The product has been declared adulterated and Not of Standard Quality (NSQ), the statement said. The minister said
The SIT investigating the cough syrup tragedy that claimed the lives of 24 children in Madhya Pradesh has arrested the wife of accused Dr Praveen Soni, an official said on Tuesday. Chhindwara-based Dr Soni, who allegedly prescribed the contaminated cough syrup 'Coldrif' to most of the ailing kids, was arrested last month for alleged negligence in connection with the child deaths due to kidney failure. His wife Jyoti Soni, another accused in the case, was arrested from her residence in Parasia town of Chhindwara district on Monday night, Sub Divisional Office of Police and Special Investigation Team (SIT) in-charge Jitendra Jaat said. She is the proprietor of a medical shop from where the cough syrup was sold to several victims, the official said. So far, seven persons have been arrested in connection with the cough syrup tragedy, he added. Following the child deaths, the Tamil Nadu government revoked the licence of the cough syrup manufacturing company, Sresan Pharma. Those arres
Amid child deaths linked to a toxic cough syrup in Madhya Pradesh, a government hospital here is now facing a complaint over worms allegedly found in a bottle of antibiotic medicine given to a child, officials said on Thursday. Following a complaint by a woman whose child was given the medicine, the entire stock of Azithromycin antibiotic at the government hospital in Morar town of Gwalior district has been sealed and samples have been sent to a laboratory in Bhopal for testing, they said. Azithromycin antibiotic's oral suspension is commonly given to children for various infections. According to officials, the medicine was generic and manufactured by a Madhya Pradesh-based company. Drug inspector Anubhuti Sharma said, "A woman at the government hospital in Morar complained of worms in a bottle of Azithromycin oral suspension." Although the bottle of medicine that the woman had brought was open, the matter was immediately investigated, she said. All 306 bottles of this medicine,
The investigation against the Kanchipuram-based manufacturer of Coldrif cough syrup, linked to the deaths of children in Madhya Pradesh, has brought to light lapses by the Tamil Nadu Food and Drug Administration in enforcing basic regulatory norms, CDSCO sources said. Licensed in 2011 by the Tamil Nadu Food and Drug Administration (TNFDA), Sresan Pharma continued operations unchecked for over a decade despite its dismal infrastructure and multiple violations of national drug safety rules, they said. A recent inspection by the Central Drugs Standard Control Organisation (CDSCO) exposed the unit's appalling conditions and total non-compliance with Good Manufacturing Practices (GMP), the sources said. "The CDSCO has not been involved in any of the audits at Sresan Pharma. Since the CDSCO was not involved and the state FDA did not inform the CDSCO about this company in any way, this company was not part of any of the CDSCO databases," a source said. TNFDA officials could not be reached