Alternative Information Directory
Coronavirus information & resources
Vaccines - What You Need To Know

A tiny sampling of DEATHS reported to the Vaccine Adverse Reporting System after injection of the COVID-19 "vaccines" as of 9-Aug-2021

Anyone considering being injected, or having their children injected with the gene therapy cocktails that are being called "vaccines" against the alleged SARS-CoV-2 virus, which has a 99.9% survival rate without any treatment, should first do their homework. If you don't know how to use the CDC's Vaccine Adverse Event Reporting System (VAERS) database, see Vaccines - What You Need To Know: Accessing The VAERS Database.

Following is a tiny sampling of VAERS event reports for females following the COVID-19 "vaccines". Currently there are 5,561 events using following criteria:

Event Category: Death
Sex: Female
Vaccine Products: COVID19 VACCINE (COVID19)
VAERS ID: All

Vaccine administered with no immediate adverse reaction at 11:29am. Vaccine screening questions were completed and resident was not feeling sick and temperature was 98F. At approximately 1:30pm the resident passed away.

Within 24 hours of receiving the vaccine, fever and respiratory distress, and anxiety developed requiring oxygen, morphine and ativan. My Mom passed away on the evening of 12/26/2020.

Patient was a 16yr female who received Pfizer vaccine 3/19/21 at vaccine clinic and presented with ongoing CPR to the ED 3/28/21 after cardiac arrest at home. Patient placed on ECMO and imaging revealed bilateral large pulmonary embolism as likely etiology of arrest. Risk factors included oral contraceptive use. Labs have since confirmed absence of Factor V leiden or prothrombin gene mutation. Patient declared dead by neurologic criteria 3/30/21.

Death due to a Subarachnoid hemorrhage

Cerebral vein thrombosis; This is a spontaneous report from a non-contactable consumer via Regulatory Authority (RA), downloaded from the Regulatory Authority-WEB, regulatory authority number DE-PEI-CADR2021061101. Sender's (Case) Safety Report Unique Identifier DE-PEI-202100053266. A 28-year-old female patient received BNT162B2 (COMIRNATY) via an unspecified route of administration on 01May2021 at 08:00 (at the age of 28-year-old) (Batch/Lot Number: EX3510) at 0.3 mL single dose for COVID-19 immunisation. Relevant medical history and concomitant medications were not reported. On 01May2021, the patient experienced cerebral vein thrombosis (thrombosis of venous sinuses) with fatal outcome. The patient died on 01May2021 at 14:30.

pt was a nursing home pt. pt received first dose of covid vaccine. pt was monitored for 15 minutes after getting shot. staff reported that pt was 15 days post covid. Pt passed away with in 90 minutes of getting vaccine

pt received vaccine at covid clinic on 12/30 at approximately 3:30, pt vomited 4 minutes after receiving shot--dark brown vomit, staff reported pt had vomited night before. Per staff report pt became short of breath between 6 and 7 pm that night. Pt had DNR on file. pt passed away at approximately 10pm. Staff reported pt was 14 + days post covid

Resident received vaccine per pharmacy at the facility at 5 pm. Approximately 6:45 resident found unresponsive and EMS contacted. Upon EMS arrival at facility, resident went into cardiac arrest, code initiated by EMS and transported to hospital. Resident expired at hospital at approximately 8 pm

Resident received vaccine in am and expired that afternoon.

Resident found unresponsive without pulse, respirations at 04:30 CPR performed, expired at 04:52 by Rescue

syncopal episode - arrested - CPR - death

Patient presented 5/16/2021 with 1 week dizziness, fever and sore throat, found to have acute myopericarditis c/b cardiogenic shock and bradycardic arrest.

Resident exhibited no adverse events during 30 minute monitoring following vaccine administration. Resident found without pulse at 1900.

Vaccine received at about 0900 on 01/04/2021 at her place of work, Medical Center, where she was employed as a housekeeper. About one hour after receiving the vaccine she experienced a hot flash, nausea, and feeling like she was going to pass out after she had bent down. Later at about 1500 hours she appeared tired and lethargic, then a short time later, at about 1600 hours, upon arrival to a friends home she complained of feeling hot and having difficulty breathing. She then collapsed, then when medics arrived, she was still breathing slowly then went into cardiac arrest and was unable to be revived.

Sudden death; This is a spontaneous report from a contactable physician and consumer. A 41-year-old female patient received the first dose of BNT162B2 (COMIRNATY; Lot Number: UNKNOWN), via an unspecified route of administration on 30Dec2020 at 0.3 mL single dose for COVID-19 immunisation. Medical history included hypertension. The patient's concomitant medications were not reported. On 01Jan2021, the patient experienced sudden death.

Patient had been diagnosed with COVID-19 on Dec. 11th, 2020. Symptoms were thought to have started on 12/5/2020. Received Moderna vaccine on 12/23. Unexpected death on 1/8/2021. Resuscitation attempts unsuccessful

Cardiac event, 2 days after vaccination, patient expired.

found dead; This spontaneous case was reported by a consumer and describes the occurrence of DEATH (found dead) in a 22-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 032m20a) for COVID-19 vaccination. Concurrent medical conditions included Traumatic brain injury, Movement disorder, Seizures (since she was a baby at 11 months old) and Speech loss. Concomitant products included CLONAZEPAM, OXCARBAZEPINE (TRILEPTAL) and GABAPENTIN for an unknown indication. On 19-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. Death occurred on 04-Apr-2021

Fever, shortness of breath and chest pain that resulted in a heart attack a few hours after vaccination

Patient received COVID vaccination around 12:15pm. Patient was monitored for the appropriate amount of time by nursing staff. Patient passed away at 2:15pm.

RECIEVED VACCINE 1/8/21 EXPIRED UNEXPECTED 1/10/21, NO ADVERSE REACTIONS NOTED

"1-2-2021 10:30 PM Complained Right arm/back hurt - took Tylenol 1-3-2021 Complained Right arm hurt, dizzy 1-4-2021 Felt better - did laundry, daughter found her deceased at 3:30 pm. Dr. at hospital said it was ""cardiac event"" according to death certificate."

Acute anterior MI with death

Cardiac arrest; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority (RA)-WEB, regulatory authority number NO-NOMAADVRE-FHI-2021-Uwzy12. A 29-year-old female patient received BNT162b2 (COMIRNATY, Solution for injection, Lot number- EX6564) intramuscularly on 07May2021 as 2nd dose, single dose (at the age of 29-years-old) for COVID-19 immunization. Patient medical history included intellectual disability from an unknown date and ongoing. The concomitant medications were not reported. Historical vaccine included BNT162b2 (COMIRNATY, Solution for injection, Lot number- UNKNOWN) via an unspecified route of administration as 1st dose, single dose for COVID-19 immunization. The patient experienced cardiac arrest on 17May2021, the patient fell the same day as the vaccination (07May2021) and this resulted in back pain afterwards.

DEATH FROM BLOOD CLOT

atient had massive acute intracranial hemorrhage. Was found down in bathroom. In ED CT scan showed large intraventricular hemorrhage, EVD placed, patient progressed to massive brain swelling and infarctions, decompressive craniectomy, unable to control intracranial pressure, parents agreed to DNR status and patient is not expected to survive.

This regulatory authority case was reported by a physician and describes the occurrence of PULMONARY EMBOLISM (PULMONARY EMBOLISM, PULMONARY INFARCTION, CARDIAC ARREST), CARDIAC ARREST (PULMONARY EMBOLISM, PULMONARY INFARCTION, CARDIAC ARREST) and PULMONARY INFARCTION (PULMONARY EMBOLISM, PULMONARY INFARCTION, CARDIAC ARREST) in a 24-year-old female patient who received mRNA-1273 (COVID 19 Vaccine Moderna) (batch no. 31946) for COVID-19 immunisation. No medical history was reported by the reporter.

The first dose of vaccine (lot number EW0176) was taken on 05/06/2021, and the second dose of vaccine (lot number EW0186) was taken on 05/27/2021. within 12 hours of second does she had gotten severe headache, she couldn't eat for severe vomiting, she said she felt like she was hit by a truck, and had the chills. she would go from really cold to really hot. She couldn't keep anything down even water. On the third day after the vaccine she was very sick and we ( the family) thought she was sleeping but when we went to try and wake her up we discovered her dead.

Lower extremity deep vein thromboses, pulmonary thromboses, cerebral thromboses and hemorrhage, death

Patient received COVID-19 (Moderna) vaccine from the Health Department on afternoon of January 8, 2021 and went to sleep approximately 2300 that night. Was found unresponsive in bed the following morning and pronounced dead at 1336 on January 9, 2021

Resident had seizure like activity followed by a vagel response with large bowel movement. Resident then began to show signs of blood clot to left lower extremity. No pedal pulse, area on leg warm to touch. Left lower leg now cold to touch, stiff, purple and white in color. No other signs of modeling, body warm to touch, no fever noted. Respirations and pulse increased with low oxygen levels. Resident not responding to stimuli.

Patient received the 1st dose of Moderna and was found deceased in her home the next day.

RESIDENT 1ST DOSE OF MODERNA VACCINE ADMINISTERED ON 01/04/2021 AT 8:30PM, RESIDENT FOUND UNRESPONSIVE ON 01/05/2021.

on 1/8/2021 17:30 patient taken to ER, cerebellar hemorrhage, stroke, aneurysm

"Cardiac Arrest; Patient was found pulseless and breathless 20 minutes following the vaccine administration.

This person was found to be deceased on routine rounds during the night, 3am. No symptoms of reaction noted post vaccine. No injection site reaction. No reports of any allergic reaction.

No adverse effects from vaccination seen on 1/2/21. On 1/6/21 resident was seen by Dr and her baclofen pump was refilled with 20 ml Baclofen 4,000mcg/ml. ITB Rate increased by 6% to 455.5 mcg/day simple continuous rate over 3 days. On 1/8/21 at 0615 resident was shaking, lower extremities mottled, Sa02 70%, pulse 45. Oxygen started at 2 L/m per NC. At 0715 her primary physician was notified as well as her daughter. Oxygen increased to 4 L/min, sats at 83%. SOA noted, reported all over pain. At 0850 when they attempted to reposition the resident, she was not responsive. Licensed nurse assessed her and no heartbeat heard or pulse found.

Initial pain in back of head and extreme headache. Some vomiting. At emergency, went into coma and was intubated. Hole drilled in skull to relieve pressure. MRI taken. Lot of bleeding in brain - anuerism lead to death approximately 14 hours after initial symptoms.

On 1/11/21 noted with headache, nausea/vomiting, severe melaise. On 1/12/21 resident expired.

71yo female resident who died after receiving Pfizer BioNTech vaccine. On 1/14/2021, VS taken at 10am, B/P 99/60, O2 sats, 95% (trach w/O2). At 11:30am, Patient showed no s/sx of distress, A&Ox3. At 11:50am, a nurse went to perform a COVID test and assessment (the facility is experiencing an outbreak), and found the patient unresponsive on the bathroom floor. CPR was immediately started; no shock advised per AED; 12:15pm EMS arrived and took over. At 12:38pm, EMT called time of death.

Resident received Moderna vaccine on 12/23/2020 around 5 pm. At approximately 3:35 am on 12/25/2020, resident had a CVA and died on 1/1/2021 at 3:00 am.

Around 00:50am on 01/15/21, C.N.A. reported that the resident looked different and not responding. Initiated Code Blue and started CPR. 911 arrived and pronounced resident dead at 1:01 am.

Letal death; Asystolia; Pulmonary embolism; This is a spontaneous report from a non-contactable physician downloaded from the Medicines Agency (MA) WEB (DE-PEI-PEI2021000071). An 82-year-old female patient received BNT162B2 (COMIRNATY; Lot number: EJ6797), intramuscularly from 30Dec2020 at 0.3 mL, single for COVID-19 immunization. Medical history included diabetes and hypertension. The patient's concomitant medications were not reported. At the time of vaccination there was no evidence of decompensation of the underlying disease. The patient experienced letal death, asystolia and pulmonary embolism on 31Dec2020, which were reported as life-threatening and fatal.

Resident received vaccination on January 15, 2021. She was found unresponsive with shallow respirations on the morning of January 16, 2021 and was sent to ER via ambulance. The resident was admitted to medical center ICU where she passed away later that day.

COVID 19 Vaccination administered by pharmacy staff. No adverse effect at the present time. Staff will continue to observe adverse reaction. Will continue to monitor. Patient at start of shift awake in the bed. Pt at 3am was on the commode leaned to the side. Patient body still warm to touch no pulse.

Cardiac arrest; This is a spontaneous report received from a contactable other HCP by Pfizer from the Regulatory Authority. The regulatory authority report number is GB-MHRA-ADR 24593178. A 53-years-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EL0379, Expiry date: Apr2021, use by 16Jan2021, 09:50), via an unspecified route of administration on 14Jan2021 at single dose for covid-19 immunization. The patient had no known previous medical history.

At 8 weeks pregnancy (2 weeks after first shot) started bleeding and had a subchorionic hematoma. By 10 week subchorionic hematoma resolved. Received second shot and of Feb. 1 week later, at 12 weeks pregnancy , fetus had no heart beat! It measured normal size (as expected) and limited normal first trimester anatomy by ultrasound. But NO heart beat. Something insulted this placenta to lead to fetal demise.

Died January 21 after she received an mRNA shot; A spontaneous report was received from a consumer via social media concerning a 28-year-old, female patient who received Moderna's COVID-19 vaccine (mRNA-1273) and died two days later (death).

Death 5 hours after second shot. Decedent contacted her mother around 3:30 c/o difficulty breathing. Died on 4/1/20

Patient reported difficulty breathing and chest pain; suffered cardiac arrest and death

Blood clot blocking blood flow to brain - 1st episode: ( 3/12/21) stabilized, minor limited movement left side - 2nd episode: (3/24/21) no blood flow to brain, death (maintained on life support for organ donation)

Leave a Reply

Your email address will not be published. Required fields are marked *