A heartbreaking incident has rocked Rajasthan as a six-year-old child from Churu died in Jaipur after reportedly consuming cough syrup. The child was hospitalized with convulsions and respiratory distress, and health officials have identified this death as the fourth of its kind linked to the same type of cough medication within the past ten days.
Authorities say the cough syrup in question contains dextromethorphan, a substance commonly used in pediatric formulations, but one that is now under scrutiny. The Health Minister of Rajasthan has claimed that laboratory tests show the syrup conformed to quality standards and stated it has been used by over 130,000 patients without adverse effects.
Nevertheless, the recurrence of these deaths has raised serious concerns regarding drug safety protocols, inspection systems, and public health surveillance. Families in affected districts report that their children fell suddenly ill after consumption and could not be saved despite immediate medical attention.
In response, an inquiry has been initiated in Rajasthan to trace the origin of the syrup, examine distribution chains, and suspend any manufacturing or supply linked to the suspected batch. Multiple states have already banned the product temporarily, pending results of toxicology tests.
This tragedy compounds a growing pattern: just days ago, two children died in Sikar and Bharatpur after reportedly taking the same cough medicine. In those cases local authorities have suspended a government doctor and pharmacist for prescribing it. New prescribing guidelines have also been issued to prevent such incidents.
The health ministry at the federal level has now advised that cough and cold medicines should not be prescribed or dispensed to children under two years. For older children prescriptions must be handled with extreme caution, and only after a careful risk assessment.
This crisis should serve as a warning: weak regulatory vigilance, lapses in drug quality assurance, and insufficient monitoring can carry fatal consequences. The state must act swiftly and transparently. Every link in the chain from production to prescription must be scrutinised. Children’s lives cannot be collateral damage of regulation failures.
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