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New Delhi: The GST rate cuts announced last week will make medicines used for the treatment of critical conditions like multiple myeloma, lung cancer, blood cancer, lymphoma, Gaucher disease, Pompe disease and haemophilia significantly cheaper and help more patients to avail of treatment, health experts said. A pack of leukaemia drug asciminib 60 (40 mg tablets), which used to cost ₹2,35,000 with GST, will become cheaper by ₹25,000, as per data from market research firm PharmaTrac. Obinutuzu ...Read More >
New Delhi, Aug 25 (PTI) Commercial and prohibited speeches are not covered under the fundamental right, the Supreme Court on Monday said as it asked five social media influencers, including "India's Got Latent" host Samay Raina, to display their unconditional apology in their podcasts or shows for ridiculing persons with disabilities and rare genetic disorders. A bench of Justices Surya Kant and Joymalya Bagchi said the degree of repentance should be higher than the degree of offending and made ...Read More >
New Delhi, Jul 15 (PTI) Five social media influencers, including "India's Got Latent" host Samay Raina, on Tuesday appeared before the Supreme Court in a case seeking action against them for ridiculing persons suffering from disabilities. A bench of Justices Surya Kant and Joymalya Bagchi recorded their presence and directed them to file their replies to the petition. They are accused of poking fun at the disabled and those suffering from Spinal Muscular Atrophy (SMA) and blindness. They were ...Read More >
New Delhi: Five social media influencers, including "India's Got Latent" host Samay Raina, on Tuesday appeared before the Supreme Court in a case seeking action against them for ridiculing persons suffering from disabilities. A bench of Justices Surya Kant and Joymalya Bagchi recorded their presence and directed them to file their replies to the petition. They are accused of poking fun at the disabled and those suffering from Spinal Muscular Atrophy (SMA) and blindness. They were directed to ag ...Read More >
Advocacy group urges swift implementation of procurement process to benefit patients Cure SMA Foundation of India, a parent-led patient advocacy organisation for Spinal Muscular Atrophy (SMA), has commended recent steps taken by the Government of India, the judiciary, and healthcare stakeholders to address rare diseases. The Ministry of Health and Family Welfare and the Delhi High Court have allocated over Rs 900 crore for rare disease treatment, including SMA, marking a milestone for the com ...Read More >
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