DM2022 0263
DM2022 0263
DM2022 0263
Department of Health
OFFICE OF THE SECRETARY
27 June 2022
DEPARTMENT MEMORANDUM
No. 2022-163
TO: ALL UNDERSECRETARIES AND ASSISTANT SECRETARIES;
DIRECTORS OF BUREAUS, SERVICES AND CENTERS FOR
HEALTH DEVELOPMENT: MINISTER OF HEALTH —
RATIONALE
Building 1, San Lazaro Compound, Rizal Avenue, Sta. Cruz, 1003 Manila @ Trunk Line 651-7800 local 1113, 1108, 1135 Direct
Line: 711-9502; 711-9503 Fax: 743-1829 @ URL: http://www.doh.gov.ph; e-mail: [email protected] ++
public and private, on the management and administration of Pfizer BioNTech
COVID-19 vaccine booster doses to non-immunocompromised Pediatric A3 and to
the Rest of the Pediatric Population (ROPP).
Il. OBJECTIVES
GENERAL GUIDELINES
. The National COVID-19 Vaccine Deployment and Vaccination Program shall adopt
future EUA or regulatory amendments from the FDA and recommendations from the
HTAC on the provision of the additional/booster doses to the pediatric population.
A. Eligible Groups
1, The eligible pediatric vaccine recipients ages 12-17 years old for the
administration of booster doses are:
a. non-immunocompromised Pediatric A3
b. Rest of the Pediatric Population (ROPP)
C. Vaccination Rollout
The LGUs shall reactivate fixed vaccination sites and establish temporary posts
in catchment areas / barangays to ensure administration of booster doses to
eligible vaccine recipients.
The administration of booster doses to non-immunocompromised Pediatric A3
and ROPP ages 12-17 years old shall be conducted simultaneously with the
ongoing house-to-house vaccination activities.
1. All implementing units and vaccination sites shall ensure that all members of the
vaccination teams undergo capacity building before rolling out of vaccination
activities.
1. The NVOC shall allocate and distribute COVID-19 vaccines for the
administration of booster doses based on the number of eligible populations
which are computed based on the recommended dose interval.
The CHDs and LGUs may utilize available Pfizer COVID-19 vaccines for 12
years old and older for the administration of the COVID-19 vaccine booster
doses, and ensure the availability of these vaccines at all times.
3. The RVOCs or the CHDs may allocate and distribute COVID-19 vaccines
directly to implementing units and vaccination sites, in coordination with the
LGUs.
1. Vaccination card with complete details of the administered two doses of the
primary series.
Valid identification cards or documents with a photo of the parent/guardian and
the vaccine recipient. (See Annex A for the list of valid identification cards or
documents)
Document/s to prove filiation. (See Annex B for the list of acceptable documents)
1. The vaccination site shall be large enough to accommodate the presence of the
vaccine recipient’s parent/guardian.
If the vaccination site is also vaccinating the adult population, a separate lane
shall be prepared and assigned for the vaccination of the vaccine recipients ages
12-17 years old.
I. Vaccination Process
1. The vaccination process and AEFI monitoring and case management shall
primarily follow the steps stipulated in the DOH’s Administrative Order No.
2022-0005, otherwise known as “Omnibus Guidelines on the Implementation of
the National Deployment and Vaccination Plan (NDVP) for COVID-19
Vaccines” , Department Circular No. 2021-0483 or the “Jnterim Operational
Guidelines on the COVID-19 Vaccination of the Rest of the Pediatric Population
Ages 12-17 Years Old,” and Department Memorandum No. 2022-0041 or the
“Interim Guidelines on the Management and Administration of Tozinameran
COVID-19 mRNA vaccine (nucleoside-modified) {Cominarty] Pfizer COVID-19
~ Vaccine
to Pediatric Population Ages 5-11 Years Old” and other relevant policies
issued by the DOH.
If the vaccine recipient did not give his/her assent, he/she shall not be coerced to
receive the additional COVID-19 vaccine dose.
In case the vaccine recipient is not capable of giving assent due to neurological
comorbidities and moderate to severe intellectual impairment, the parent or the
authorized parental substitute can sign on his/her behalf.
All LVOCs and LGUs are instructed to simplify the processes in the vaccination
sites for the administration of COVID-19 vaccine booster doses. The following
directives are being reiterated:
i. Ask the vaccine recipient due to be given with first booster dose the
following documents ONLY:
1. Original vaccination card showing the completion of the primary
dose series
2. Any valid identification card
i. The health education and informed consent step can be integrated with
other steps to streamline the processes in the vaccination site.
ii. Provide health education/information materials in any area of the
vaccination site, especially in the waiting area and post-vaccination
monitoring area.
ili. Ensure that a health educator is available at all times to provide vaccine
recipients with the necessary information and to answer any questions.
iv. The informed consent may be signed in the registration area or in the
health screening area, after health education.
Vii. For the administration of booster doses, the vaccine recipient may be
screened prior to the vaccination proper. There are two ways in which the
vaccine recipient shall be screened:
1. Review the informed consent form and make sure that it is properly
signed.
2. Review thoroughly the health screening form and the eligibility of the
vaccine recipient, by asking relevant questions and physically
assessing the vaccine patient. If the vaccine recipient is not eligible,
defer the vaccination and provide an appropriate schedule or refer to
the appropriate vaccination site.
3. Review the information on the vaccination card. Determine the date
and the vaccine brand of the primary dose series and the first booster
dose administered. Calculate the dose interval.
d. Post-Vaccination Monitoring
i. Check the contents of the AEFI Kit. Ensure completeness of the kit.
ii. Observe the vaccine recipient for any Adverse Event Following
Immunization (AEFI).
iv. Ensure that the vaccine recipient is essentially well before leaving the
vaccination site.
y. Provide appropriate intervention to manage AEFI.
vi. Encode allinformation of the vaccine recipients (by the encoder) based on
the data requirements.
J. Vaccination Reporting
1. All vaccination sites shall categorize the vaccinated pediatric population ages
12-17 years old based on their previous Priority Groups:
a. Pediatric A3 (for non-immunocompromised Pediatric A3)
10
b. Rest of the Pediatric Population
2. All LGUs shall submit the required data requirements to the Vaccine
Administration System (VAS - Line List) and Vaccination Operations Reporting
System (VORS) on a daily basis.
3. The VORS and VAS line list data fields shall be updated to include the
additional/booster dose.
2. LGUs and all Implementing Units shall maximize both online and offline
platforms, and promote community engagement through targeted COVID-19
vaccination key messaging, and prioritization of those Most-at-Risk Population
(MARP).
3. CHDs/RVOCs/LVOCs and LGUs are highly encouraged to engage with the local
medical societies, faith-based organizations, and other relevant stakeholders in
health promotion activities relating to COVID-19 vaccination.
4. CHDs and LGUs shall ensure feedback mechanisms and social listening by
promoting the use of the Knowledge Informs Responsible Action or Katuwang
na Impormasyon para sa Responsableng Aksyon (KIRA) chatbot
(hitps://m.me/OfficialDOHgov).
5. All implementing units are directed to calibrate and/or recalibrate their existing
crisis communication plans, in accordance with DM 2021-0224, otherwise
known
as, Interim Guidelines in Adverse Events Following Immunization (AEFI)
Community Management and Crisis Communications Related to COVID-19
Vaccines.
11
For dissemination and strict compliance.
12
ANNEX
A. LIST OF VALID IDENTIFICATION CARDS OR DOCUMENTS
Valid identification cards or documents with photo of the parent/guardian and the vaccine
recipient to verify documents shall be presented. These are the list of valid identification cards of
parent/guardian:
1. SSS Card
2. GSIS Card
9. Senior Citizen ID
13. Others
ANNEX B. REQUIREMENTS TO PROVE FILIATION/ GUARDIANSHIP FOR
PEDIATRIC COVID-19 VACCINATION
A.At least one (1) of the following documents shall be presented to prove filiation or
guardianship:
a. The best evidence of filiation for the accompanying parent shall be an original
copy or a certified true copy of the Birth Certificate issued by the Philippine
Statistics Authority (PSA). In lieu of the PSA-issued Birth Certificate or certified
true copy of the same, a copy of the Certification issued by the Local Civil
Registrar of the City or Municipality where the vaccine recipient was registered
shall be acceptable. The Certification shall set forth the following:
v. Sex;
b. In case the vaccine recipient does not have a copy of the original or certified true
copy of his/her birth certificate or a Certification from the Local Civil Registrar,
secondary documents shall be acceptable as long as the same is coupled with a
valid government identification card issued to the parent and the vaccine
recipient. The following are the secondary documents that may be presented (The
list is not in order of preference):
il. Baptismal Certificate of the child with the name of the parent/s;
ili. School ID or records of the child (transcript of records, Form 137, etc.)
bearing the name of the parent;
Vi. Barangay Certification issued by the Barangay Captain indicating that the
parent/s and the child is personally known to
the latter and setting forth the
filiation of the said individuals, as attested by one (1) other witness who
personally knows the child and the parent;
Vii. If the parent is a Solo Parent, a copy of the Solo Parent identification card
from the City or Municipal Social Welfare and Development Office, a
Local Social Welfare and Development Office, Tallaq or Faskh
certification from the Shariah court or any Muslim Barangay or
religious
leader, provided that the name ofthe child is indicated therein;
1X. PWD ID of the child, if available, wherein the name of the parent is
indicated in the ID pursuant to DOH AO No. 2017-0008 or the
“Implementing Guidelines of Republic Act 10754, otherwise known as “An
Act Expanding the Benefits and Privileges of Persons with Disability”, for
the Provision of Medical and Health-related Discounts and Special
Privileges;
c. In case the parent is residing abroad or cannot accompany their own children on
the day of the scheduled vaccination, the accompanying adult may present a
Special Power of Attorney executed by either parent of the minor designating the
minor’s companion to assist in the vaccination process. (If executed abroad, the
SPA must be apostilled, if applicable, or authenticated by the Philippine
Embassy/Consulate). The following documents may serve as an alternative
document to
the Special Power of Attorney:
il. written affidavit of parent /guardian under an oath with a public official
such as the notary public or a person authorized to do so (eg. Barangay
Officials) with presentation of a valid government ID; or
2. In case the minor is accompanied by his/her legal or judicial guardian (The list is
not in order of preference):
Affidavit of Kinship;
Authenticated medical certificate of the child bearing the name of the guardian,
issued by the hospital or the DOH;
School ID or record of the child which bears the name of the guardian;
PhilHealth, SSS, GSIS forms indicating that the vaccine recipient is
a beneficiary
and a child under the guardianship of the accompanying adult. In lieu of physical
copies, the parent may show his/her online account of the PhilHealth, SSS and
GSIS online portal showing his/herrelationship with the child;
i. Copies of insurance policies, health card membership, life plan, memorial plan
and similar policies wherein the vaccine recipient is the child under the
guardianship of the accompanying adult and the said policies were taken on
behalf of the latter. In lieu of physical copies, the parent may show his/her online
account of the online portal of the said service and health providers, showing
his/her relationship with the child;
b. The Child-Caring Agency may also opt to provide the DOH a certified list of the
names of the minor vaccine recipients who will be vaccinated and the name of
their authorized accompanying adults, attaching photocopies of their valid IDs. If
so, both the vaccine recipients and the accompanying heads/officers shall be
required to present the actual valid government ID corresponding to the one
submitted by the Agency. For the accompanying heads/officers, they shall be
required to present the valid ID issued by the Child-Caring Agency issued under
their name.
In case the above-mentioned mechanisms are not feasible, based on the assessment of the
vaccination team after it has conducted due diligence in ensuring that the vaccine recipient
has difficulty in obtaining the primary documents, the accompanying adult and the vaccine
recipient shall present the following documents:
School ID or record of the child which bears the name of the accompanying
heads/officers;
For purposes of verifying the identity of the accompanying adult, the valid ID
issued by the Child-Caring Agency and a separate government issued ID shall be
presented by the latter..
ANNEX C. COVID-19 PEDIATRIC VACCINATION - 17 YEARS OLD) (12
ADDITIONAL/ BOOSTER DOSE INFORMED CONSENT FORM FOR
PFIZER-BIONTECH (may be accessed through bit.ly/PediaBoosterForms)
Vaccination Site:
Section 1: Information on the risks and benefits of Cases of myocarditis reported to the US Vaccine
the Pfizer-BioNTech COVID-19 vaccine Adverse Event Reporting System (VAERS) have
additional/booster dose occurred after MRNA COVID-19 vaccination, especially
in male adolescents and young adults. more often after
The Philippine Food and Drug Administration has the second dose usually within several days after
authorized the emergency use of the Pfizer-BioNTech vaccination. Most patients with myocarditis or
COVID-19 vaccine to individuals 12 years and older pericarditis who received care responded well to
under an Emergency Use Authorization (EUA). An medicine and rest and felt better quickly.
additional/booster dose of Pfizer-BioNTech may be
administered 5-6 months after the second dose of the Despite the side effects, recent studies show that
primary dose series or 28 days after the second dose the benefits of receiving the additional/booster
for immunocompromised individuals. The vaccine may dose of Pfizer-BioNTech COVID-19 vaccine far
prevent the person vaccinated from getting severe outweigh the risks.
COVID-19 infection and hospitalization.
Section 2: Parent's/Guardian’s Consent for Minor’s
Side effects that have been reported with the Vaccination
Pfizer-BioNTech COVID-19 vaccine include: injection
site pain, redness, itching, and swelling: tiredness: | confirm that | have been provided with and have read
headache; muscle pain, chills, joint pain; fever; nausea: the Pfizer-BioNTech COVID-19 vaccine Emergency
vomiting; diarrhea: feeling unwell; arm pain, insomnia, Use Authorization (EUA) Information Sheet and the
decreased appetite, excessive sweating, night sweats, same has been explained to me. The Philippine FDA
enlarged lymph nodes. There is a remote chance that has amended the EUA to allow its use as an
the vaccine cowld cause temporary one-sided facial additional/booster dose for the pediatric population
drooping and/or severe allergic reaction such as hives aged 12-17 in light of new scientific evidence.
or swelling of the face. A severe allergic reaction would
usually occur within a few minutes to one hour after | confirm that the minor has been screened for
geting a dose of the PYizer-BioNTech COVID-19 conditions that may merit deferment or special
vaccine. For this reason, the vaccine provider may ask precautions for additional/booster dose vaccination as
ihe recipient to stay at the vaccination site for indicated in the Health Screening Questionnaire.
monitoring post-vaccination
| have received sufficient information on the benefits
The United States Center for Disease Control and and risks of receiving an additional/booster dose of the
Prevention (US CDC} and its partners are actively COVID-19 vaccine and | understand the possible risks
monitoring reports of myocarditis and pericarditis after if the minor is not vaccinated with an additional’booster
COVID-19 vaccination. dose.
Myocarditis is the inflammation of the heart muscle, ‘was provided an opportunity to ask questions, all of
and pericarditis is the inflammation of the outer lining of which were adequately and clearly answered. |,
the heart. In both cases, the body's immune system therefore, voluntarily release the Government of the
causes inflammation in response to an infection or Philippines, the vaccine manufacturer, their agents and
some other triggers. Both myocarditis and pericarditis employees, as well as the hospital, the medical doctors
have the following symptoms: chest pain, shoriness of and vaccinators, from all claims relating to the results of
breath, feelings of having a fast-beating, fluttering, or the use and administration of, or the ineffectiveness of
pounding of the heart. the additional/booster dose of FPfizer-BioNTech
COVID-19 vaccine.
=
ANNEX D. COVID-19 PEDIATRIC VACCINATION - 17 YEARS OLD) (12
ADDITIONAL/ BOOSTER DOSE ASSENT FORM FOR PFIZER-BIONTECH
(may be accessed through bit.ly/PediaBoosterForms)
o
COVID-19 PEDIATRIC VACCINATION (12-17 YEARS OLD) ADDITIONAL/BOOSTER DOSE
INFORMED CONSENT FORM AND ASSENT FORM FOR PFIZER-BIONTECH
of the Philippine National COVID-T9 Vaocine Deployment and Vaccination Program
asof June 20, 2022
tundenstand that while most side effects aer miner and Section 3: Minors Assent for Vaccination
resolve om ther own, Sere is a small risk of severe
Siverse reactions, such as, but mot bimited to allergies | ACKNOWLEDGE THAT:
and that showld prompt medical attertion be mended,
referral $o the megrest hospital shall be prowidled tam being asked te deckte it |,
immediately by the Goverment of the Phiippines. |
have been given comtact information for follow up for
any symetoms which may be experienced after (Minors Mame)
waeocinahon
> Want to neorhwe the additionaliboostes
i
understand that by signing this Form, the minor has a ose of the Pizer-BioN Tech COWID. 1D
vacomnr.
might bo health benefit packages under the Philpore (Age. years)
Mevlth Insurance Corporation (PhiMeakh) in case
fhefshe suffers a severe andior serious adverse event
which
t
Ptaer oNTech
fownd to
COVID 18
be associated with the
weecing or its:
{have understood the
additionaiiboomer
information about the
dose of the Pfizer BioN Tech
adminisination. | understand that the night to claim COVID- 18 wancine which wall be vaccinated tc me, and |
compersation ts subject the guidelines
to of PaiMeaith confirm that) have understood the same
ihereby give consent to the additional/booster cose Iwan to receive the COVID 19 waocine at this time
waocination of the mince mamed abowe with the i] W the minor is not
capabic of giving assent due
Pier Bion Tech COVID-1S vaccine. | affirm that | have to neweological comortinites and moderate to
understood and reviewed the informa@ton included in sevens intellectua! impairment, the parent or tie
Section herein. (Hf thes comment is mot signed. dated
to
authorized parental substitute can sign an
and returned. fhe eninar will mot be weocinabed) iéissher behalf,
Signature ower Printed Namie of the Paront’Guardian Signature over Printed Name of the Minor / Parent!
‘Guardian
Dato Date
Hyou choase motto hawe your childwarnd vaccinated, please It you choose not to get vaccinated. please lst down the
isa Gown the reasons: reasons:
ANNEX E. COVID-19 PEDIATRIC VACCINATION(12 - 17 YEARS OLD)
ADDITIONAL/ BOOSTER DOSE HEALTH DECLARATION SCREENING FORM FOR
PFIZER-BIONTECH (may be accessed through bit.ly/PediaBoosterForms)
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