Use of Meropenem drug can cause adverse reactions: Health ministry panel
Health ministry plans central online drug registry to avoid medication error caused by similar namesMeropenem drug is available under various brand names in India. The medicine falls under the schedule H and H1 of the drugs and cosmetic rules, 1945 and required to be sold by retail only under the prescription by a doctor.“The analysis of adverse drug reactions from Pharmacovigilance Programme of India (PvPI) database revealed that Meropenem drug to cause adverse drug reaction," stated IPC’s drug safety alert reviewed by Mint.“Healthcare professionals, patients or consumers are advised to closely monitor the possibility of the above ADR associated with the use of above suspected drug.
If such a reaction is encountered, please report to the IPC," it said.“The pack inserts in Pfizer’s meropenem drug formulation already contains safety alert for acute generalised exanthematous pustulosis (AGEP). Patient Safety is our priority and we are committed to working with authorities to deliver quality products that meet the highest standards of safety and efficacy," Pfizer’s spokesperson said.Also Read: Uniform rates in pvt hospitals across all states an uphill task, as majority do not implement CEA: Health ministry“Whenever adverse reactions are reported due to the use of drugs that must be reported to the government," said one of the state drug controllers requesting anonymity.IPC monitors adverse drug reactions among Indian population and helps the Central Drugs Standard Control Organization (CDSCO) in taking regulatory decisions for safe use of medicines.Meanwhile, to regulate the misuse of antibiotics the regulator Drugs Controller General of India has directed states/UT governments to keep a close watch on the sale of
. Read more on livemint.com
