Updated: May 22
*Note: 83% of VAERS Reports are generated from medical providers, state reporting agencies, and pharmaceutical companies. European reporting systems are documenting exponentially higher rates than VAERS data, as the 30 year old monitoring system captures only 1% of post vaccination injuries per Harvard research report. Low capture rate is central issue with CDC VAERS system not credibility. FDA has admitted the mass vaccination program began without adequate safety monitoring system.
Unite4Truth will be on break from 5/23 - 5/28 - Please keep the word out by sharing our past posts from the Truth Blogger HERE.
-The FDA is now holding over 100 million Johnson & Johnson Covid-19 Janssen vaccines over 'contamination concerns'. It was originally reported in early April that Emergent BioSolutions had put active ingredient components of AstraZeneca vaccination in over 15 million J& J doses. For full story on Johnson & Johnson vaccine contamination, please see HERE.
-India's mucormycosis infection rate continues to intensify with India's central government now declaring the infection an epidemic. The highly rare black fungal infection has gone from single digits cases to infecting many thousands. Public health officials claims of spread due to use of steroids and immune compromised status of those with attributed Covid-19 infections does not sufficiently explain origin with the infections now occurring in multiple municipalities. Murcormycosis infections outbreaks are usually localized. For full coverage of India's murcormysosis outbreak and correlating oxygen crisis please see HERE.
-Doctors file motion to immediately halt administration of Covid-19 vaccinations in children under 16. American Frontline Doctors submitted a request for a temporary restraining order against youth administration of Covid-19 vaccination in Alabama on May 20th. Read the legal request HERE.
-Children's Health Defense has launched a citizen's petition to halt administration of all Covid-19 vaccinations. Please help the effort by commenting and signing the petition. Full article with links to petition may be found HERE.
-Oregon is going to require citizens to show proof of vaccination in order to enter businesses or require individuals to wear masks indoors, a policy based on a unsubstantiated theory of 'asymptomatic' transmission. Evidence demonstrates high rates of individuals testing positive for Sars CoV2 with non-specific PCR testing has been due to FDA recommendations that set Cycle Threshold levels at high levels which produce majority false positives by default. For a full review of severe problems with the Covid-19 testing programs and discussion on asymptomatic transmission, go HERE & HERE.
-Moderna ingredient release documents presence of lipid SM-102 as part of formulation, chemical ingredient that is not approved for human and animal use according to the manufacturer safety sheet for the product.
The Moderna COVID-19 Vaccine is made of the following ingredients:
mRNA – Like the Pfizer BioNTech vaccine, Moderna’s also uses mRNA technology to build antibodies against COVID-19.
Lipids – The Moderna vaccine also requires lipids to help deliver the mRNA to the cells.
1,2-dimyristoyl-rac-glycero3-methoxypolyethylene glycol-2000 [PEG2000-DMG]
-Sudden hearing loss is now being reported by some Covid-19 vaccination recipients
The current VAERS total for the week of 5/14/2021:
Adverse events reports increased by cases in one week: 34,338
*Multiple reports may be submitted for one event, researchers have flagged issue with data system implicating potential under counting of total events
Total Adverse event reports: 1,009,051
Total individual events counted: 227,112
Total Death event reports: 19,554
Total individual death events counted: 4,647
Time period between Covid-19 vaccine administration and death: (Breakdown of 4,063 deaths reported on VAERS data, CDC has not yet released all death VAERS report on system - total death number from weekly selected CDC events reports)
0 Days: 541
1 Day : 662
Over 25% (1,203) deaths occurred within minutes to one day (up to 48 hrs) post Covid-19 vaccination,
2 Days: 733
3 Days: 463
4 Days: 347
5 Days: 286
6 Days: 220
7 Days: 246
72.7% (2957) deaths occurred within one week post Covid-19 vaccination
Total Life Threatening Event Reports: 97124
Total Individual Life Threatening Events Reported: 13,354
Chart of Top Life Threatening Post Covid-19 Vaccination Symptoms: Reports for Week Ending 5/7/2021:
Total Hospitalization event reports: 392,857
Total Individual Hospitalization events counted: 49,965
Guillian Barre Syndrome 10th Most Common Symptom for Hospitalization with 2,546 case reports
Chart for Post Covid-19 Hospitalizations for week ending 5/7/2021
Total Permanent Disability total event reports: 102.259
Total Permanent Disability individual case counted: 14,596
Total Emergency Room even reports: 262,494
Total Emergency Room individual events counted: 42,697
VAERS total Pfizer-Biontech Week Ending 5/07/2021
Total Adverse event reports: 378,331
Total individual events counted: 87,420
Death event reports 9,036 Total individual death events counted: 1,739
Life threatening event report total: 13,360
Life threatening event individual events counted: 1,813
Total Hospitalization event reports: 41,855
Total Individual Hospitalization events counted: 5,733
1,923 individuals were hospitalized within minutes to one day post Pfizer vaccination
Total Permanent Disability event reports: 9,483
Total Permanent Disability individual case counted: 1,385
Total Emergency Room even reports: 83,715
Total Emergency Room individual events counted: 14,013
Pfizer Biontech Individual Case Review:
*It has been up to this period, considered an ethical breach to include vulnerable population groups in investigative drug programs. Pfizer Biontech has Emergency, Investigative Use only permission by the FDA, and early administration has now launched safety investigation for myocarditis, blood clotting issues, and thrombocytopenia induction through use of this new technology mRNA drug (Moderna also mRNA drug). Individuals receiving all Covid-19 vaccinations should be aware they are participating in a defacto trial with data utilized to inform safety investigation and final approval submission to the FDA.
Post Pfizer Deaths & Injuries include:
27 year old man with Down Syndrome, No Prior Significant Medical History, Presented with symptoms three days post Pfizer vaccination including myopericarditis (Pfizer & Moderana vacciantions are currently under global investigation for induction myocarditis, report HERE.
"27 year old male with Down's Syndrome and no other past medical history received second COVID-19 vaccine on 4/27/2021. On 4/30/2021 began ""feeling poorly"" with nausea/vomiting and possible chest discomfort. Originally presented to ED on morning of 4/30 - EKG completed demonstrated diffused ST elevation. Patient was transferred to Medical Center for heart catheterization. Left heart catheterization demonstrated normal coronary arteries and LVEDP of 25. Stat ECHO demonstrated pericardial effusion and concern raised for myopericarditis. Patient subsequently transferred to a different Medical Center for higher level of care. Upon arrival to Medical Center plan was to intubate and take to cath lab for heart biopsy and PA catheter placement. However, upon intubation patient began to decompensate and subsequently developed cardiac arrest. During ACLS, VA ECMO was placed and therapeutic hypothermia was initiated. Following VA ECMO placement patient received IVIG, high dose methylprednisolone (1000 mg), anakinra 100 mg, and broad spectrum antibiotics (vancomycin and Zosyn). Despite these efforts the patient continued to have hemodynamic instability and was on high dose vasopressors (epinephrine, norepinephrine, dopamine, angiotensin II, vasopressin). Patient subsequently suffered another cardiac arrest, briefly regained pulse with high dose vasopressors, but subsequently lost pulse despite best efforts and died on 5/1/2021 at approximately 13:00."
Full VAERS Report HERE:
29 year old Arizona female with no prior significant medical history noted died, one day post Pfizer vaccination, with renal & cardiac failure:
"Patient described myalgias, headache and dyspnea at ER visit on 4/1/21 at 2:37 am. Patient was discharged. Patient returned the same day at 15:40 cyanotic, altered, hypoxic and hypotensive. The patient was found to have profound metabolic acidosis, liver failure, renal failure. She went into cardiopulmonary arrest, was revived, rearrested and died. Patient was treated for possible sepsis, shock, liver failure"
A 17 year old teenager fr0m Hawaii began having seizures post Pfizer Biontech vacciantion and underwent prolonged hospitalization (not noted in summary, only in medical notes):
"Began having seizures; Presented to the ER on 17 March 2021 for headache with blurry vision; Presented to the ER on 17 March 2021 for headache with blurry vision; Also had persistent nausea and subsequent vomiting; Also had persistent nausea and subsequent vomiting; Fever X1 to 100.4F on day of presentation/no further sz; This is a spontaneous report from a contactable physician. A 17-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) intramuscularly in right arm on 08Mar2021 (lot number: EN6206) at single dose for COVID-19 immunization. Medical history included headache and irregular periods, ongoing hospitalization. No known allergies. Concomitant medications included birth control pills. No other vaccine in four weeks. No COVID prior vaccination. Vaccine received during existing hospitalization. The patient began having seizures (hospitalization prolonged, life threatening) on 16Mar2021 12:00, presented to the ER on 17Mar2021 for headache with blurry vision (hospitalization prolonged, life threatening) on 16Mar2021 12:00, also had persistent nausea and subsequent vomiting (hospitalization prolonged, life threatening) on 16Mar2021 12:00, fever x1 to 100.4F on day of presentation/no further seizure (hospitalization prolonged, life threatening) on 16Mar2021 12:00. Clinical course: Presented to the ER on 17March2021 for headache with blurry vision. Patient reported symptoms for 1 day prior. Also had persistent nausea and subsequent vomiting. Presented to the ED at 23:00. Began having seizures. EEG shows localized to the occipital region. Fever X1 to 100.4F on day of presentation no further sz. LP shows 1 WBC, Gram stain negative. Cultures negative. HSV pending. On ceftriaxone and acyclovir. Continues to have focal sz on EEG now on 3 AEDs. MRI with contrast negative. CBC unremarkable. CRP elevated to 0.8 (normal less than 0.5). Tox screen negative. COVID tested post vaccination: Nasal Swab (SARS-CoV-2 Cepheid) with result of negative on 17Mar2021. Therapeutic measures were taken as a result of all the events which included treatment with IVIG, Antibiotics, Steroids, Antiepileptics. The outcome of the events was not recovered.; Sender's Comments: Based on the information currently available, a possible contributory role of the suspect drug to the reported events cannot be completely excluded based on temporal association and known drug safety profile. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate"
Full VAERS note submitted from physician:
Moderna Covid-19 Vaccine for Week Ending 5/07/2021
Total Adverse event reports: 468,284
Total individual events counted: 106,269
Death event report total: 8,797
Death event individual events counted: 1984
Life threatening event report total: 11,167
Life threatening event individual events counted: 1,462
Total Hospitalization event reports: 37,815
Total Individual Hospitalization events counted: 5,516
Total Permanent Disability event reports: 7,249
Total Permanent Disability individual case counted: 1,020
Total Emergency Room even reports: 70,203
Total Emergency Room individual events counted: 11,385
Individual Case Review Moderna Covid-19 Vaccination:
35 Year Old Pregnant, no significant past medical history or labor complications noted, died during normal labor two week post administration of Moderna Covid-19 vaccination, autopsy pending:
"Due date 4/18/2021. Pt presented in labor on 4/10/21. Her labor was uncomplicated and progressing appropriately. She had sudden onset of coughing following by loss of consciousness. Code blue was called. Emergency bedside C/S was performed. Despite resuscitative efforts of 1 hour and 15 minutes, the patient expired".
VAERS total Johnson & Johnson Janssen Covid-19 Vaccination for Week Ending 5/07/2021
Total Adverse event reports: 154,403
Total individual events counted: 33,324
Total death event reports: 1,599
Total individual deaths reports counted: 315
Life threatening event report total: 4,816
Life threatening event individual events counted:
Total Hospitalization event reports: 13,611
Total Individual Hospitalization events counted: 1616
Total Permanent Disability event reports: 2438
Total Permanent Disability individual case counted: 307
Chart of Top Injuries Resulting in Permanent Disability Post Janssen Covid-19 Vaccination:
Total Emergency Room even reports: 28,126
Total Emergency Room individual events counted: 4166
Individual Case Review Johnson & Johnson Vaccine:
49 year old female died same day as vaccine administration, no significant medical history noted:
DEATH; This spontaneous report received from a company representative concerned a 49 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included the patient had no known drug allergies. The patient received covid-19 vaccine ad26.cov2. s (suspension for injection, route of admin not reported, batch number: Unknown) dose was not reported, frequency 1 total, administered on MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 27-APR-2021, the patient died from unknown cause of death after 4 weeks of Johnson and Johnson vaccination. An autopsy was performed on an unspecified date and there was no sign of high blood pressure, heart disease, or diabetes to patient as per report. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. This report was serious (Death).; Sender's Comments: V0. 20210505962-covid-19 vaccine ad26.cov2.s -Death. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).; Reported Cause(s) of Death: UNKNOWN CAUSE OF DEATH; Autopsy-determined Cause(s) of Death: UNKNOWN CAUSE OF DEATH
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Please sign and share Health Professionals for Covid-19 Policy Correction to end all unnecessary and harmful Covid-19 health directives:
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