CAG to apex court: state can use its report in Yeddyurappa cases

February 27, 2017

New Delhi, Feb 27: The Comptroller and Auditor General (CAG) has told the Supreme Court that the state government and its prosecuting agencies are free to take any decision on its reports relating to land denotifications undertaken during the tenure of the then chief minister B S Yeddyurappa.

Yeddyurappa“The issue whether the report of the CAG could be made basis for initiation of criminal proceedings is a matter which would fall within the domain of the state government and its prosecuting agencies,” it said in an affidavit filed in the apex court. The stand taken by the CAG comes in support of the Karnataka government which, in its special leave petition, contended that the reports prepared by the constitutional body could be relied upon for initiating action for “cognisable offence” against Yeddyurappa.

The CAG’s affidavit came in response to a notice issued by the Supreme Court, which has been hearing the Karnataka government’s petition challenging the Karnataka High Court’s single-judge bench order of January 5, 2016.

The CAG submitted that it has undertaken performance audit on denotification of land by the state government and allotment of sites by the Bangalore Development Authority (BDA). The audit findings were based on a sample determined at 40% of 126 denotification cases done by the government during 2007-12. The CAG also said its performance audit on land management was taken across the country in eight states and was not limited to Karnataka.

Allowing a batch of 15 petitions by Yeddyurappa, the high court had then held the CAG report could not be the basis for registration of FIRs relating to denotification of lands acquired by the BDA in Bilekahalli, Halagavaderahalli, J B Kaval and other places in Bengaluru city when he was the chief minister.

Yeddyurappa, on his part, has denied before the court any wrongdoing in passing orders for various denotification of land. He claimed the registration of 15 FIRs on the direction by the Lokayukta on the basis of CAG’s reports was “completely misplaced” and has rightly been quashed by the Karnataka High Court.

Responding to the apex court’s notice, Yeddyurappa said, “The CAG report cannot be the sole basis of registration of the FIR. Since the reports (2010-11 and 2012) submitted to the governor on November 21, 2012, is in the process of consideration of the Public Accounts Committee, no other authority can act upon the said report.”

Comments

Skazi
 - 
Monday, 27 Feb 2017

Yeddy .... Be careful before barking and showing fingers at others ..... All politicians are naked in the bath rooms ....

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News Network
July 17,2020

Bengaluru, Jul 17: The Doctors at Fortis Hospital, here on Friday, successfully treated a 97-year-old patient who suffered an embolic stroke due to calcified stenosis (narrowing of an artery resulting in restriction of blood flow).

In a release, the Hospital authorities stated that the team of doctors led by Dr Rajpal Singh, Director and Interventional Cardiologist, Fortis Hospital, Bangalore successfully conducted Carotid Artery Stenting (CAS) to increase the blood flow in the blocked areas which had resulted in stroke following stringent safety protocols and ensuring proper segregation of COVID and Non-COVID patients at the hospital.

Carotid arteries serve as the main channels which supply the blood flow to the brain and facial structures. Any significant narrowing in these arteries can cause a brain stroke, a mini-stroke, headache, and neurological symptoms.

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coastaldigest.com web desk
July 1,2020

The United States of America has bought almost the entire world's supply of remdesivir, one of just two drugs proven to treat COVID-19. 

“President Trump has struck an amazing deal to ensure Americans have access to the first authorised therapeutic for Covid-19,” said the US health and human services secretary, Alex Azar. 

“To the extent possible, we want to ensure that any American patient who needs remdesivir can get it. The Trump administration is doing everything in our power to learn more about life-saving therapeutics for Covid-19 and secure access to these options for the American people.”

The announcement implies that no other country in the world will be able to buy remdesivir for next three months at least.

The anti-viral drug patented by the US-based Gilead biotech firm is the only one approved by the European Medicines Agency (EMA) to treat patients with the novel coronavirus.

The Trump administration has already shown that it is prepared to outbid and outmanoeuvre all other countries to secure the medical supplies it needs for the US.

“They’ve got access to most of the drug supply [of remdesivir], so there’s nothing for Europe,” said Dr Andrew Hill, senior visiting research fellow at Liverpool University.

Remdesivir, the first drug approved by licensing authorities in the US to treat Covid-19, is made by Gilead and has been shown to help people recover faster from the disease. 

The first 140,000 doses, supplied to drug trials around the world, have been used up. The Trump administration has now bought more than 500,000 doses, which is all of Gilead’s production for July and 90% of August and September.

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News Network
July 6,2020

Mangaluru, Jul 6: Two fresh deaths in last 24 hours have taken the total number of covid-19 deaths in Dakshina Kannada district to 24.

The deceased are a 52-year-old woman from Ullal and a 52-year-old man from Thokkottu.

The man was suffering from cardovascular disease and pneumonia, sources said.

The woman passed away in Wenlock hospital.

More details are awaited.

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