Uttar Pradesh Bans Coldrif Cough Syrup Following Child Deaths in Madhya Pradesh

1 min read     Updated on 06 Oct 2025, 07:39 AM
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Overview

Uttar Pradesh government has banned Coldrif cough syrup, manufactured by Shreesan Pharmaceutical Ltd, following 14 children's deaths in Madhya Pradesh. UP has ordered sample collection for testing and prohibited import/export of the syrup. MP police formed a special investigation team. The Union health ministry held a meeting with states to review drug quality compliance. ICMR Director General advised against prescribing cough syrups to children.

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*this image is generated using AI for illustrative purposes only.

In a significant move, the Uttar Pradesh government has banned Coldrif cough syrup, manufactured by Shreesan Pharmaceutical Ltd, following the tragic deaths of at least 14 children in Madhya Pradesh. The fatalities have been linked to severe side effects from the consumption of this cough syrup.

Regulatory Actions and Investigations

The Uttar Pradesh government has taken swift action in response to this public health crisis:

  • The Assistant Commissioner of Drug Administration has ordered drug inspectors to collect samples from both government and private institutions for laboratory testing in Lucknow.
  • Import and export of the cough syrup have been prohibited until further notice as a precautionary measure.

In Madhya Pradesh, where the deaths occurred:

  • The police have formed a special investigation team to probe the deaths, which are suspected to be linked to renal failure caused by the cough syrup.

National Response

The incident has prompted action at the national level:

  • The Union health ministry convened a high-level meeting with all states to review drug quality compliance.
  • The meeting also focused on promoting rational use of cough syrups in children.

Medical Community's Stance

The medical community has responded to this crisis with caution:

  • The Director General of the Indian Council of Medical Research (ICMR) has advised against prescribing cough syrups to children to prevent side effects.

Implications for the Pharmaceutical Industry

This incident highlights several critical issues in the pharmaceutical sector:

Aspect Impact
Quality Control Increased scrutiny on manufacturing processes and quality assurance
Regulatory Oversight Potential for stricter regulations and more frequent inspections
Public Trust Possible erosion of confidence in over-the-counter medications
Industry Practices Re-evaluation of prescription practices for pediatric cough treatments

The ban on Coldrif cough syrup and the subsequent investigations serve as a stark reminder of the critical importance of drug safety and the potential consequences of lapses in quality control within the pharmaceutical industry. As the situation develops, it may lead to broader discussions about drug safety regulations and the need for more rigorous testing protocols, especially for medications intended for children.

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