Senators blast politicians taking advantage of COVID-19 crisis to campaign for 2022 polls

Robie de Guzman   •   April 3, 2020   •   1069

MANILA, Philippines – Minority senators on Friday lambasted politicians who are taking advantage of the novel coronavirus disease (COVID-19) crisis to advance their political agenda, hampering the speedy delivery of relief to millions of poor families.

In a joint statement, Senate Minority Leader Franklin Drilon, and Senators Francis Pangilinan and Risa Hontiveros criticized politicians who are exploiting the current public health situation to campaign for the 2022 elections, leaving millions of vulnerable and low-income Filipino families unassisted.

“It is not red tape. It is the 2022 political campaign that is hampering the immediate distribution of relief to millions of poor families,” the senators said.

The lawmakers issued the statement following complaints regarding the “sluggish” release of assistance by the Department of Social Welfare and Development (DSWD) and other government agencies.

“It saddens us that there are people who could be so heartless and power hungry as to take advantage of this crisis to advance their political ambition,” the lawmakers said.

“To presidential wannabees, hands off, please. Go away,” they added.

The senators stressed that the distribution of disaster aid and the bureaucracy is politicized when political campaign gets in the way.

“Worse, national and local officials who have shown initiative and innovation in responding to COVID-19 crisis are politicized, criticized and crucified, which would only add to the suffering of our countrymen and women,” they said.

The lawmakers also called on private corporations and charity groups to be discerning and to not allow themselves to be used for obvious political propaganda, especially during these trying times.

They also called on the DSWD and other government agencies to just use their existing database instead of distributing social amelioration cards (SAC) in implementing the government’s emergency subsidy program for the COV-19 crisis as provided in the Bayanihan to Heal as One Act.

The SAC is a form being distributed at the barangay level to capture the family profile, which will be used as the basis in providing aid to the affected families.

“Let us spare our fellow Filipinos this unnecessary procedure. Our kababayans are getting hungry and desperate for help. They lost jobs. Give the aid ASAP,” they said.

IATF places Cagayan, Apayao, Benguet back to MECQ due to high COVID-19 cases

Aileen Cerrudo   •   May 11, 2021

MANILA, Philippines—Northern provinces Cagayan, Apayao, and Benguet have reverted to modified enhanced community quarantine (MECQ) after recording high cases of coronavirus disease (COVID-19).

The MECQ status will take effect on May 11 until May 23.

As of May 10, Cagayan has 4,657 cases followed by Benguet with 531 and Apayao with 63.

Business operations in the said areas will be limited according to the directive of the Inter-Agency Task Force on the Emerging Infectious Diseases (IATF-EID).

A liquor ban will be implemented while religious gatherings will only be allowed at 10% capacity.  Entertainment and recreational events also be suspended.

Benguet governor Melchor Diclas reported that majority of the COVID-19 cases in their area are severe. Hospitals in Benguet are also in short supply of respirators.

“Dumadami talaga ang mga pasyente natin. Marami ang namamatay at marami ang nagkakasakit ng critical at serious. Ang respirator natin may nagagamit tayong 13 na respirator. Ang bakante nalang ay dalawa,” he said.

(Our patients are increasing. Many have died and many are in critical or serious condition. We have 13 respirators but there are only two available units left.)

Hospitals in Apayao, meanwhile, are at 80% critical level.  In Cagayan Province, Governor Manuel Mamba said Tuguegarao City’s home quarantine setup is still contributing to the rising cases of COVID-19.

“Hindi magiging epektibo ang MECQ sa Tuguegarao City hangga’t may home quarantine,” he said.

(MECQ in Tuguegarao City will not be effective as long as home quarantine is being implemented .)

Mamba continues to reiterate the need to build isolation facilities in Tuguegarao to accommodate COVID-19 patients. AAC (With reports from Marvin Calas)

 

 

Evaluation of EUA application for Sinopharm vax may be completed in less than 21 days – FDA

Robie de Guzman   •   May 11, 2021

MANILA, Philippines – The evaluation process for the Sinopharm COVID-19 vaccine will not take long before it can be granted an emergency use authorization (EUA) in the Philippines, the Food and Drug Administration (FDA) said Tuesday.

FDA director-general Eric Domingo said the Sinopharm vaccine has already been included in the emergency use listing (EUL) of the World Health Organization (WHO) and access to its documents, including inspection reports from the WHO will be faster.

“Useful yung kanyang Emergency Use Listing sa WHO kasi before this, wala pa siyang EUA from a stringent regulatory authority katulad ng mga USFDA ganyan or Europe, Japan… hindi pa siya listed sa mga iyon. Pero yung WHO na emergency use listing that’s equivalent to a stringent regulatory authority,” he said.

“Ang maganda sa WHO kasi very transparent ang documents nyan. Available din siya sa FDA. Lahat ng ni-review nila, maaari naming ma-access kaya hindi tayo masyado mahihirapan sa paghingi ng information,” he added.

The Department of Health (DOH) earlier said it has started the process of applying for EUA, pending documents about the vaccine product.

The FDA said the process may take less than 21 days once the DOH completes the application process.

“Kapag ganyan na merong WHO EUL, mas mapapabilis iyan. Nakakaya natin iyan usually less than 21 days,” Domingo said.

The FDA also echoed the DOH’s earlier statement that there are no irregularities with the government’s move to file an EUA for a Chinese-made vaccine since they also applied for the EUA of other COVID-19 vaccine brands, such as Sinovac, AstraZeneca, and Pfizer, in order for these vaccines to be delivered to the country.

“Talagang nasa batas and it’s a worldwide practice,” he said. “Based on WHO guidelines, posible naman na gobyerno gusto bumili ng bakuna na walang local manufacturer or representative dito. In those cases, the government itself can get EUA.”

“Hindi naman conflict yun dahil ang EUA ay hindi naman product registration o marketing authorization lang, talagang for emergency use lang ang mga bakuna,” he added. – RRD (with details from Correspondent Aiko Miguel)

Palace welcomes WHO’s emergency use listing for Sinopharm COVID-19 vaccine

Robie de Guzman   •   May 11, 2021

MANILA, Philippines – Malacañang on Tuesday welcomed the decision of the World Health Organization (WHO) to approve Sinopharm’s COVID-19 vaccine for emergency use listing (EUL).

In a statement, Presidential Spokesperson Harry Roque said this development will strengthen the country’s vaccine portfolio.

“We welcome the Emergency Use Listing (EUL) of the World Health Organization for Sinopharm. This development would strengthen our diversified vaccine portfolio as we continue to work on improving access to safe and effective vaccines, including Sinopharm,” Roque said.

A WHO emergency listing means that a product’s safety and efficacy has been rigorously evaluated. It will also allow the product to be included in the COVAX facility for faster global roll out.

The COVAX facility led by the WHO is a global program that seeks to provide vaccine supply mainly for poor countries.

The emergency use listing will also allow countries to expedite their own regulatory approval to import and administer COVID-19 vaccines.

The Philippines has so far received more than 7.5 million doses of COVID-19 vaccines and more are expected to arrive in the next few weeks.

“With the arrival of the bulk of our vaccine orders in the coming months, we are confident that we would be able to speed up our coronavirus vaccination program,” Roque said.

The Department of Health earlier said the emergency use authorization (EUA) application for Sinopharm vaccine is now being processed.

The Food and Drug Administration said the application’s evaluation will not take long as the product is already under the WHO emergency use listing.

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