General
Opposition chief blames Kerala govt for generic SMA drug mishandling
Reported by Abhishek Tiwari (Copy Editor) · The Hindu - National ·
Reported by one source so far
Opposition leader Pinarayi Vijayan accused the Kerala government of lapses and lack of transparency in the distribution of the generic SMA drug Risdiplam at SAT Hospital. He said the government ignored a letter from parents of children with spinal muscular atrophy that raised concerns over the sudden change of medicine. Vijayan claimed the Health Minister tried to paint the criticism as an attack on generic drugs, while the real issue is the failure to follow proper safeguards in drug purchase. He noted that the new administration approved the generic drug in July 2026, despite SAT Hospital officials stating the decision to buy Natco’s generic had been finalised in February 2026 under the previous Left government. Vijayan questioned whether the required procedures were observed and reiterated allegations that “clinical trial drugs” were handed to children, warning that such actions heighten parental anxiety. He demanded a full explanation of how trial‑stage medicines entered the public supply and why parents were not informed. The leader urged the government to disclose all facts, insisting that children must not be turned into subjects of experimentation.
Context
SMA is a rare genetic disorder that weakens muscles; Risdiplam is an approved treatment whose high cost can be reduced by generic versions. Transparent procurement and clear communication are essential to maintain public trust in health programmes.
ExplainerWhy this matters
What Happened
Opposition leader Pinarayi Vijayan says the Kerala government approved a generic version of the SMA drug Risdiplam in July 2026, although the decision to buy Natco’s generic was already made in February 2026 under the previous Left government. He alleges that the Health Minister ignored parents’ concerns and that medicines meant for clinical trials were given to children at SAT Hospital.
Why It Matters
SMA requires costly treatment; generic drugs can make therapy affordable for families. When a government bypasses standard procurement steps or fails to inform parents, it raises doubts about safety, creates anxiety, and can erode confidence in public health programmes.
What Happens Next
Vijayan has demanded a detailed explanation from the Health Ministry. The issue may lead to a parliamentary inquiry or legal scrutiny of the drug‑purchase process, and could prompt the government to review its guidelines for introducing generic medicines.
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