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Wednesday, December 31, 2025 1:38 AM

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Dr. Reddy’s unveils cancer drug in U.S.

Lenalidomide capsules, a generic version of the popular multiple myeloma drug Revlimid, have been introduced to the US market, according to pharma giant Dr Reddy’s Laboratories, which on Wednesday informed the stock markets. According to Dr. Reddy’s, with this volume-restricted launch, two (2.5 mg and 20 mg) out of the six strengths it has introduced for the medicine in the US market are qualified for first to market, 180 days of generic drug exclusivity. The company launched the cancer medication in the US in the following strengths: 2.5 mg, 5 mg, and 10 mg, each in a bottle count size of 28 capsules; 15 mg, 20 mg, and 25 mg, each in a bottle count size of 21. In September 2020, Dr. Reddy’s and Celgene, a fully owned subsidiary of BMS, reached a patent settlement for Revlimid, a drug with annual sales of around $12.80 billion USD. In settlement of all unresolved claims in its litigation, “Celgene agreed to provide Dr Reddy’s a licence to sell volume limited amounts of generic lenalidomide capsules in the US,” Dr Reddy’s stated.

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AI might lessen common drug side effects

Article on Health

According to the study, a research team has created a tool that measures the negative effects of medications using natural language processing, an artificial intelligence methodology, and chemical structure analysis. The new tool is made to determine which medications are more likely to cause anticholinergic side effects, which affect the brain by inhibiting acetylcholine, a key neurotransmitter. Professor Chris Fox from the University of Exeter in the UK stated, “Use of medicines with anticholinergic effects can have significant harmful effects for example falls and confusion, which are avoidable, we urgently need to reduce the harmful side effects as this can lead to hospitalisation and death.” “This new tool provides a promising avenue towards a more tailored personalised medicine approach, of ensuring the right person gets a safe and effective treatment while avoiding unwanted anticholinergic effects”, he added. Antidepressants, stomach medications, bladder medications, and Parkinson’s disease treatments for elderly individuals are a few examples of over-the-counter drugs that can have anti-cholinergic side effects. Confusion, blurred vision, light-headedness, falls, and a decline in brain function are some of the side effects. Long-term usage of it may potentially increase the risk of dementia. According to research reported in the journal Age and Ageing, the tool evaluates anticholinergic burden by allocating a score based on reported adverse events and closely matching the chemical make-up of the drug being considered for prescription. This scoring system is more precise and up to date than any prior system. In addition, the researchers surveyed 110 medical specialists, including pharmacists and nurses who write prescriptions. When asked if they would utilise a tool to evaluate the risk of anticholinergic side effects, 85% of this group responded in the affirmative. To further enhance the tool, the team also gathered usability feedback. According to Dr. Saber Sami of the University of East Anglia, “Our tool is the first to use innovative artificial intelligence technology in measures of anticholinergic burden, ultimately, once further research has been conducted the tool should support pharmacists and prescribing health professionals in finding the best treatment for patients.” Source: IANS

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Indian pharma market grew by 12.1% in August: AWACS report

According to market research firm AWACS, the Indian pharmaceutical market (IPM) increased in value by 12.1% and volume by 4.8% in the month of August as a result of strong growth across all therapy areas. In August, IPM had sales of Rs 16,239 crore. The pharmaceutical industry has increased prices for medicines subject to price regulation and infectious diseases associated with the monsoon due to the wholesale price index (WPI) inflation linked price hike permitted by the government. The categories with the fastest growth rates were cardiac (13% growth), anti-infectives (13% growth), and gastrointestinal (12% growth). Vitamin sales and anti-diabetes sales both increased by 9%. The top three selling brands in India continue to be Abbott’s Mixtard, GSK’s Augmentin, and USV’s Glycomet.

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Cost of cervical cancer vaccine set to be Rs 200-400

Scientific completion suggests that the vaccine’s R&D efforts are finished, and that the next step would be to make the vaccine accessible to the general population. According to Union minister of science and technology Jitendra Singh, Covid has increased public knowledge of preventative healthcare, which has facilitated the creation of vaccinations such as the one against cervical cancer. “The schemes like Ayushman Bharat have made us think about preventive healthcare and we can now afford it. The Department of Biotechnology has taken a lead in the matter and are in collaborative mode,” he said. “Scientific efforts at times do not get the scale of recognition they deserve. So this event is to celebrate that scientific completion,” he said. Outside of the occasion, Poonawalla met with reporters and stated, “The cost of the cervical cancer vaccine, which will range between Rs 200 to 400, will be reasonable. However, the exact cost will only be determined following thorough negotiations with the government “. In comparison to existing cervical cancer vaccinations, he said, “the vaccine would be much, much less expensive.” Poonawalla anticipated that the vaccine might go on sale by the year’s end. He stated that the vaccine will first be made available through the government channel, then starting the next year, certain private partners would also be involved. Poonawalla added that a plan to produce 200 million doses is in place. The vaccine will initially be administered in India, and only when the demands of the country have been met, will it be exported to other countries. In order to test this vaccination, 2000 people from all over the nation participated, according to Rajesh Gokhale, secretary of the department of biotechnology. Source: PTI

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Lupin receives USFDA approval for a generic cancer treatment drug

On Monday, Lupin announced that it has got a tentative approval from the US health regulator to offer Dasatinib tablets, which are used to treat specific forms of cancer, in the US. Dasatinib tablets in strengths of 20 mg, 50 mg, 70 mg, 80 mg, 100 mg, and 140 mg have been approved by the US Food and Drug Administration (FDA), the company in partnership with Pharmascience Inc. stated in a statement. The medicine produced by the Mumbai-based company is a generic version of the Sprycel tablets sold by Bristol-Myers Squibb Company. Dasatinib tablets had an estimated annual sale of USD 1,569 million in the US, according to IQVIA MAT data. On the BSE, shares of Lupin closed at Rs 662.50 each, up 1.49 percent. Source: PTI

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Pfizer’s vaccine against a deadly respiratory virus has shown positive results

A vaccine against the respiratory syncytial virus (RSV), for which there are presently no authorized shots, showed promising results in elderly patients on Thursday, according to pharmaceutical behemoth Pfizer. The virus can cause pneumonia in elderly people and causes bronchiolitis, a respiratory condition that primarily affects newborns. RSV infection causes more than 177,000 older patients to be hospitalised each year in the US, and 14,000 of them eventually die, according to US health authorities. In an ongoing clinical trial, the vaccine is being evaluated on individuals 60 years of age and older. A preliminary investigation revealed that it was roughly 85% successful in averting severe cases, or those with three or more symptoms. In the upcoming months, Pfizer said it intends to submit applications for the vaccine to the US Food and Drug Administration and other regulatory bodies. “Scientists and researchers have worked to develop RSV vaccines with little success for over half a century. These findings are an important step in our effort to help protect against RSV disease,” Pfizer’s chief scientific officer, Annaliesa Anderson, who oversees vaccine development, stated in a statement. The company reported that the vaccination was well received and that there were no safety issues. They added that they would submit the findings for publication in a scientific journal. Out of the anticipated 40,000 participants, around 37,000 have already been enrolled in the clinical trial. The vaccine, which targets two strains of the virus, is given to half of them, while the other half receives a placebo. In addition to Moderna, other companies are striving to create an RSV vaccine.

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Dolo 650 maker claims that less than Rs 10 crore was spent on promotions

The maker of the Dolo 650, Micro Labs, claims that it spent a pittance on the brand’s marketing and promotion, spending less than Rs 10 crore annually. Micro Labs is the subject of a controversy over allegations of unethical business practises. The Bangalore-based company was under scrutiny last week during a hearing in another case brought by the Federation of Medical and Sales Representatives Association before the Supreme Court. The corporation is accused of giving doctors freebies worth over Rs 1,000 crore. During the pandemic, the Rs 2 pill became well-known for providing pain and fever relief. Its sales for the fiscal year that ended in March this year totalled Rs 362 crore, an increase of over 30%. “Dolo 650 is a mega brand due to first-mover advantage, its quality, availability and reach across the country. It is a mass brand and an established market leader with 50% share, even before Covid,” said Dilip Surana, the CMD of Micro Labs. The offices of the Rs 4,500 crore Micro Labs were raided and the premises searched by the tax department last month on suspicion of tax evasion. In total, the company has spent Rs 1000 crore on marketing for all of its products, not just Dolo 650. “On the pain relief pill alone, the marketing expenditure has typically been 4-5% of its annual turnover of Rs 200-250 crore,” said Executive VP (Marketing) Jayaraj Govindaraju. He said that the basic promotions (to doctors) during Covid were of low value and comprised handing out free (Dolo) samples, brand reminders, masks & sanitizers, and scientific dissemination through conferences on fever.

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First case of Japanese encephalitis is reported in Mizoram

Japanese encephalitis (JE), a viral brain ailment spread by mosquito bites, was first diagnosed in Mizoram on Thursday. Dr. Pachuau Lalmalsawma, the state nodal officer for the Integrated Disease Surveillance Project (IDSP), made the announcement in a statement. He stated that the National Center for Disease Control (NCDC) had recently been notified by the state health department about the discovery of a suspected JE case at Trinity Hospital and requested a final decision as it would be the first JE case in the state. According to Pachuau’s statement, “after perusing the investigation reports of the suspected patient, the NCDC has confirmed the case.” Japanese encephalitis virus (JEV) is a flavivirus that is spread by culex mosquitoes, which are also responsible for spreading dengue, yellow fever, and West Nile viruses. JEV is the primary cause of viral encephalitis in several Asian countries, according to the World Health Organization (WHO), with an estimated 68 000 clinical cases each year. Even though cases of symptomatic Japanese encephalitis (JE) are uncommon, the case-fatality rate among those who have the illness can reach 30%. The safest approach to prevent getting sick is to avoid mosquito bites by using a mosquito net, insect repellent lotion, and insecticides like dichloro-diphenyl-trichloroethane (DDT), as well as cleaning your surroundings to stop mosquito breeding, according to state health experts. Source: PTI

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Omicron-specific vaccine being developed by SII could be released by the end of the year: Report

An Omicron-specific vaccination is apparently being developed by the Serum Institute of India (SII), according to an NDTV report. The vaccine is being developed in collaboration with Novavax, according to SII Chief Executive Officer Adar Poonawalla, who spoke to NDTV. Poonawalla added that the vaccine would only protect against the Omicron sub-variant BA5. Poonawalla says that SII may introduce the vaccine in India within the next six months. “Think this vaccine is important as a booster. Trials of Novavax are in progress in Australia currently. By November-December should be in a position to approach the US drug regulator,” Poonawalla was quoted as saying by NDTV.  The COVID-19 vaccine from AstraZeneca is made by SII, the largest vaccine manufacturer in the world, and is sold under the brand name Covishield. A new Covid vaccine that targets the Omicron variant was approved earlier today by the UK, making it the first country to do so. The bivalent vaccine from Moderna, which targets both the original Covid strain and the Omicron variant, has received approval from the Medicines and Healthcare Products Regulatory Agency (MHRA), according to the Daily Mirror. The “next generation” coronavirus booster shot has been approved for use in adults and may only need to be given once a year. The Moderna vaccine, also known as mRNA-1273.214, is an updated version that is currently used for first, second, and booster doses. This dose will be the first one to be authorised in the UK that specifically targets two strains of the virus.

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100 million Corbevax doses were supplied to the centre: Biological E. Ltd

The Center has received doses of Corbevax, the COVID-19 vaccine developed by Biological E. Ltd. (BE), totaling 10 crore (100 million), the company reported on Thursday. The city-based vaccine manufacturer stated in a release: “Biological E. Limited has delivered 10 crore doses of Corbevax to the Government of India till now. PanIndia roll-out of Corbevax in children 12-14 years of age was initiated on March 16, 2022 and till now almost seven crore doses have been administered and 2.9 crore children have completed the two-dose vaccination regimen.” The Union Health Ministry also gave Corbevax approval as a heterologous COVID-19 booster dosage under emergency use authorization for people 18 years of age and older after primary immunisation (two doses) with Covaxin or Covishield, the company reported. The COVID-19 Working Group of the National Technical Advisory Group (NTAGI) on Immunization’s recent recommendations served as the foundation for the Health Ministry’s approval. From August 12, 2022, Corbevax is anticipated to be offered as a booster dosage through the CoWIN App in public and private vaccination centers. The vaccine was previously given the go-ahead for emergency use as a heterologous COVID-19 booster dosage for those age 18 and over on June 4, 2022, by the Drug Controller General of India (DCGI). In a series of approvals from December 2021 to April 2022, the vaccine had gained emergency use authorisation as the primary two-dose immunisation schedule in adults, adolescents, and children aged five and above. For private COVID-19 vaccination centers, Corbevax is available for Rs. 250, GST inclusive. The price was set at Rs 400 for the consumer, including taxes and administrative expenses. Source: PTI

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