Add Tribune As Your Trusted Source
TrendingVideosIndia
Opinions | CommentEditorialsThe MiddleLetters to the EditorReflections
UPSC | Exam ScheduleExam Mentor
State | Himachal PradeshPunjabJammu & KashmirHaryanaChhattisgarhMadhya PradeshRajasthanUttarakhandUttar Pradesh
City | ChandigarhAmritsarJalandharLudhianaDelhiPatialaBathindaShaharnama
World | ChinaUnited StatesPakistan
Diaspora
Features | The Tribune ScienceTime CapsuleSpectrumIn-DepthTravelFood
Business | My MoneyAutoZone
News Columns | Straight DriveCanada CallingLondon LetterKashmir AngleJammu JournalInside the CapitalHimachal CallingHill View
Don't Miss
Advertisement

Spurious drugs: Haryana Medical Services Corporation Ltd 'boycotts' Maiden Pharma, junks purchase orders

Unlock Exclusive Insights with The Tribune Premium

Take your experience further with Premium access. Thought-provoking Opinions, Expert Analysis, In-depth Insights and other Member Only Benefits
Yearly Premium ₹999 ₹349/Year
Yearly Premium $49 $24.99/Year
Advertisement

Bhartesh Singh Thakur

Advertisement

Advertisement

Chandigarh, October 21

The Haryana Medical Services Corporation Ltd (HMSCL), a state body that procures medicines for government hospitals and dispensaries, has blocked the orders placed with Sonepat-based Maiden Pharmaceuticals, which is under the scanner over the death of more than 66 children in Gambia.

A senior HMSCL official told The Tribune that this year’s multiple orders of Maiden Pharmaceuticals had been blocked. “The stock of medicines, including several syrups, that was procured last year will also not be used,” he said.

Advertisement

The decision was taken after the Food and Drug Administration (FDA), Haryana, ordered the firm to stop manufacturing operations. The World Health Organisation (WHO) had on October 5 issued an alert after four cough syrups of Maiden Pharmaceuticals were found contaminated with diethylene glycol and ethylene glycol.

Following this, a team of the Central Drugs Standard Control Organisation (CDSCO) inspected the firm’s records and took samples of the syrups. The FDA issued a show-cause notice to the firm on October 7 under Rule 85 (2) of the Drug Rules, 1945.

It was found that the firm had not performed quality test on solvent propylene glycol for diethylene glycol and ethylene glycol. The batch number, firm’s name and manufacturing and expiry dates were not mentioned on purchase invoices.

“The plant was found under renovation. The firm failed to produce log books of equipment and instruments used for manufacturing and testing drugs,” said the notice, adding the firm had not performed process validation and analytical method validation for products in question.

Sources said Maiden Pharmaceuticals had not yet replied to the show-cause notice even as only seven days were given to it to file the reply. The CDSCO was yet to intimate the FDA about the lab report of the cough syrups, which was also unusual, they said.

Earlier, the Rohtak PGIMS had stopped the use of omeprazole 20 mg, manufactured by Maiden Pharma Ltd, Sonepat.

Firm yet to reply to show-cause notice

Advertisement
Show comments
Advertisement