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Patanjali Coronil got approval from Ayush ministry. It can be sold as an immunity booster not as cure of COVID-19.

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The Union AYUSH Ministry on Tuesday approved the sales of Patanjali’s Coronil drug as an immunity booster and not as COVID-19 cure. The Ministry has issued Patanjali firm the license to make three medicines, Divya Coronil tablet, Divya Swasari Vati and Divya Anu oil, and also clinical trials under the rule. But in any case, Coronil cannot mention COVID-19 on its packaging and claim to cure the coronavirus infection.
The Coronil tablet was launched last Tuesday by Patanjali Ayurved for the treatment of coronavirus patients where Yoga Guru Baba Ramdev stated that Patanjali had prepared the first Ayurvedic-clinically controlled, research, evidence, and trial based medicine for COVID -19. He also mentioned that they had conducted clinically controlled trials and found out that 69% of patients recovered from COVID-19 in 3 days and 100% of patients recovered from COVID-19 in 7 days. These trials were carried out at the privately-run National Institute of Medical Sciences in Jaipur.
This claim brought about much clamor regarding Patanjali’s Coronil drug. Soon after its launch, the Ministry of AYUSH ordered Patanjali to stop advertising the product until the issue gets closely examined and scrutinized. The central government’s AYUSH Ministry later charged at Patanjali for publicizing a COVID “cure” without an appropriate license. The AYUSH Ministry of Uttarakhand on Tuesday said that the license issued to Patanjali was not to find a cure for coronavirus, but only for the production of immunity booster kits and fever medicines.
Replying to a notice sent by the Uttarakhand government, Patanjali  Ayurved on Monday claimed that it has not sold, publicized, or promoted any kit to treat coronavirus but only shared with the media the successful trial of medicine.
According to ANI reports, Acharya Balkrishna, Chairman of Patanjali Ayurved stated, “We have followed all procedures to manufacture the medicine (Coronil). We applied for the license based on classical evidence of the compounds used in the medicine. We worked on the compounds and put out the results of the clinical trial before people.” He further added, “We have not done anything wrong while obtaining the license. We did not advertise the medicine (Coronil), we just tried to tell people about the effects of the medicine.”
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Health

Expert Advice On COVID Vaccination For Children

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Mansukh Mandaviya, the Union Health Minister, announced on Saturday that the central government will begin administering COVID-19 immunisation to children aged 5 to 15 years as soon as a group of specialists makes recommendations to that effect.

When asked about the government’s immunisation policy for youngsters aged 5 to 15, Mandaviya addressed reporters in this city.

He stated that the expert panel has yet to make a recommendation about this category’s vaccination.

The minister was in town for a BJP-hosted event on the Union Budget, which was announced on February 1.

“A panel of scientists recommends when and how to vaccinate, as well as which age groups to vaccinate. Within one week, we had implemented the precaution group’s advice. We will undoubtedly put its advice (for the age group of 5 to 15) into action as soon as we receive it “During a press conference, he stated.

COVID-19 immunisation for children aged 15 to 18 years old began last month across the country.

“Vaccination is no longer a concern. There is no shortage of vaccines; there are no shortages of dosages. We will unquestionably accept the scientific community’s advice “Mandaviya threw in her two cents.

The ministry has yet to receive such a suggestion and will make a decision in the following days based on that information. It isn’t a decision based on politics. In July-August of last year, he noted, a serosurvey and seroprevalence study revealed that 67% of youngsters developed antibodies while remaining asymptomatic.

“In the end, it’s all about biology. As a result, before making recommendations, scientists do research. We used to watch the news all the time (for recommendations regarding vaccination). Our scientists today perform their research, conduct their studies, and form their conclusions “He expressed himself.

He further said that during the third wave of the pandemic, India employed immunisation to combat it quite efficiently.

The minister stated that large-scale immunisation helped India combat the third wave, as evidenced by leading institutes around the world and the Indian Council of Medical Research (ICMR).

According to him, 75% of children (15-18 years old) have had their COVID-19 immunisation shots, 96% of adults have received the first dose, and 77% have received both doses.

“Based on all of this, I can certainly say that India has been able to use vaccination very effectively to fight against the COVID-19 crisis,” he said, adding that the ICMR studies showed that COVID-19 vaccination has helped the majority of people, and as a result, the country is moving toward the flattening of the curve.

He claimed that the government’s focus on vaccination during the 2020 shutdown, which began shortly after the virus’s emergence, helped India maintain its economic economy and avoid the high inflation and negative growth witnessed in the United States and Europe.

According to Mandaviya, vaccination research was prioritised by the government, and the government provided funding for it. By January 16 of last year, India’s indigenously manufactured vaccine had been launched at the same time as vaccines created in other countries.

“India made immunisation available to the rest of the globe and even began mass-producing it. As a result, when the third wave (of the COVID-19 pandemic) arrived, we were already ahead of the game in terms of immunisation. Because India had completed 96 per cent of the first dose, we were spared in the third wave “He expressed himself.

Mandaviya, speaking about the Union Budget, said that India would enter a golden period.

“I am confident that its implementation will accelerate comprehensive and time-bound development in the correct direction,” he said.

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Chinese scientists inform about yet another type of Coronavirus

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According to a new study by Chinese researchers, a new type of coronavirus named NeoCov, that spreads among bats may pose a threat to humans in the future if it mutates further.

The study that was recently posted on the preprint repository BioRxiv shows that NeoCov is closely related to the Middle East respiratory syndrome (MERS), a viral disease first identified in Saudi Arabia in 2012.

Coronaviruses are a large family of viruses that can cause diseases ranging from the common cold to Severe Acute Respiratory Syndrome (SARS).

Researchers from the Chinese Academy of Sciences and Wuhan University noted that NeoCov is found in a population of bats and to date spreads exclusively among these animals.

In its current form, NeoCov does not infect humans but further mutations may make it potentially harmful for human life. The researchers further noted that infection with NeoCov could not be cross-neutralised by antibodies targeting the existing variants of coronavirus.

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Covid vaccines like Covaxin, Covishield to be available in hospitals

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Covaxin and Covishield will now be available in the regular market as the Drug Controller General of India have given conditional market approval to these two Covid vaccines on Thursday.

The subject expert committee of the Central Drug Standard Control Organisation has earlier recommended granting regular market approval to these Covid-19 vaccines for the adult population, subject to certain conditions. Market approval, however, does not mean that the vaccines will be available in medical shops. People will have to buy Covishield and Covaxin from hospitals and clinics.

Vaccination data has to be submitted to DCGI every six months. Data will have t to be updated on CoWIN app also. Earlier, it was reported that the Centre was planning to cap the price of the vaccines at 275 per dose.

The approval has been granted under the New Drugs and Clinical Trials Rules, 2019. The firms, in this case, Bharat Biotech (Covaxin) and Serum Institute of India (Covishield), shall submit data of ongoing clinical trials

All vaccination data will be recorded on the CoWIN platform. The approval is only for adult population.

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