CDC VAERS WONDER SYSTEM OF SEVERAL PATIENTS WHO HAVE DIES OF BECAUSE OF THE VACCINES.

 

 

VAERS ID:  0985004-1

Patient Age	79.00	Sex	Male
State / Territory	Oklahoma	Date Report Completed	2021-01-18
Date Vaccinated	2021-01-14	Date Report Received	2021-01-18
Date of Onset	2021-01-14	Date Died	2021-01-16
Days to onset	0

Vaccine Type	Vaccine	Manufacturer	Lot	Dose	Route	Site
COVID19 VACCINE	COVID19 (COVID19 (PFIZER-BIONTECH))	PFIZER\BIONTECH	NONE	UNK

ABDOMINAL PAIN UPPER	Yes	COVID19 VACCINE (COVID19)

 Daughter call in for VAERS report to file for father whom committed suicide 1/16/2021 in the AM after reportable ae of COVID 19 vaccine administered 1/14/2021. Patient sought care twice at ER; first visit by ambulance around 5PM and Friday 1/15/2021 Medical Center: Emergency Room. 1st Discharge summary diagnosis: adverse reaction to COVID shot; 2nd Discharge summary diagnosis: adverse reaction to COVID shot, fever, Panic Disorder-- ER. Medical Center Discharge summary diagnosis: Adverse reaction to the vaccine, acute anxiety. Reportable patient symptoms at, 1st visit : fever, shaking stomach cramps, breathing issues. Medical Center -- No fever, confusion and dementia type, patient would not stay in patient bed; patient would get up and sit down again repeatedly, agitated and anxious. Attempted to urinated hospital bed. Patient committed suicide in home.

ABDOMINAL PAIN UPPER	Yes	COVID19 VACCINE (COVID19)

LINK: https://wonder.cdc.gov/controller/datarequest/D8;jsessionid=4692C5FB50361E8BE82306FD46BB

VAERS ID:  0976032-1 ABDOMINAL PAIN - COVID 19 VACCINE

Patient stated he wasn't feeling well on January 25, 2021, wasn't eating and complained of abdominal pain. Patient noted to have indigestion and was constipated. Meds provided and labs ordered. On morning of January 26, 2021, patient became weak, lethargic and hypoxic and was sent to emergency department around 0700 hours on January 26, 2021. At approximately 1100 hours, emergency physician notified this writer that patient was not going to overcome his illness and would be placed on comfort care. At approximately 1130 hours, this writer was notified that patient had passed away from multi-organ failure.

Patient Age 92.00 Sex Male State / Territory California Date Report Completed 2021-01-26 Date Vaccinated 2021-01-22 Date Report Received 2021-01-26 Date of Onset 2021-01-26 Date Died 2021-01-26 Days to onset 4 Vaccine Administered By Senior Living * Vaccine Purchased By Not Applicable * Mfr/Imm Project Number NONE Report Form Version 2 Recovered No Serious Yes

Vaccine Type Vaccine Manufacturer Lot Dose Route Site COVID19 VACCINE COVID19 (COVID19 (PFIZER-BIONTECH)) PFIZER\BIONTECH EL3302 2 IM RA

VAERS ID: 0954812-1 ABDOMINAL PAIN UPPER  - COVID19 VACCINE  

She had the first dose of Pfizer vaccine at the Campus on Friday 1/15 at 4:30 pm. After the vaccine, she had no new symptoms or signs of vaccine reaction and MD friend reports that he checked her pulse which was not elevated from baseline. On 1/16, she awakened and continued to feel at her recent baseline. However, in the early afternoon, she complained of headache, nausea/epigastric pain, and chest heaviness. These apparently were not unusual symptoms for her to feel intermittently. Per her niece, who has a home O2 sat device, her 02 sat that morning was 97 with a HR of 87 irregularly irregular. She was afebrile. (continue on page 2)

 

Patient Age	86.00	Sex	Female
State / Territory	New York	Date Report Completed	2021-01-18
Date Vaccinated	2021-01-15	Date Report Received	2021-01-19
Date of Onset	2021-01-16	Date Died	2021-01-16
Days to onset	1
Vaccine Administered By	Private	Vaccine Purchased By	Not Applicable *
Mfr/Imm Project Number	NONE	Report Form Version	2
Recovered	Missing	Serious	Yes

Vaccine Type	Vaccine	Manufacturer	Lot	Dose	Route	Site
COVID19 VACCINE	COVID19 (COVID19 (PFIZER-BIONTECH))	PFIZER\BIONTECH	NONE	1	IM

Medications At Time Of Vaccination	History/Allergies
apixaban, levothyroxine, prednisone, diltiazem, (cont page 2)	non stentable distal occlusive disease, coronary heart disease, stroke, heart failure, diabetes mellitus, (cont. p 2),NKDA

VAERS ID: 0959179-1 ACUTE KIDNEY INJURY -   COVID19 VACCINE 

Patient received COVID-19 vaccination on 1/14/2021. On 1/17/2021, patient was transferred to Hospital s/p multiple cardiac arrests. Patient was hyperkalemic and in acute renal failure at time of transfer. Hyperkalemia was treated, but the patient suffered PEA vs VFib. At the time of transfer, patient was on vasopressin, norepinephrine, and epinephrine. The patient had an EF of 40-45% and elevated troponins. Patient was made DNR and placed on comfort care. Patient passed away on 1/18/2021. Ultimately we suspect that the patients condition was a direct result of his underlying disease states, but wanted to make sure reporting was made available.

Patient Age	79.00	Sex	Male
State / Territory	Colorado	Date Report Completed	2021-01-20
Date Vaccinated	2021-01-14	Date Report Received	2021-01-20
Date of Onset	2021-01-17	Date Died	2021-01-18
Days to onset	3
Vaccine Administered By	Unknown	Vaccine Purchased By	Not Applicable *
Mfr/Imm Project Number	NONE	Report Form Version	2
Recovered	No	Serious	Yes

LINK: https://wonder.cdc.gov/controller/datarequest/D8;jsessionid=4692C5FB50361E8BE82306FD46BB

VAERS ID: 0920545-1 ABNORMAL BEHAVIOR  - COVID19 VACCINE

"The resident received is vaccine around 11:00 am and tolerated it without any difficulty or immediate adverse effects. He was at therapy from 12:36 pm until 1:22 pm when he stated he was too tired and could not do anymore. The therapist took him back to his room at that time and he got into bed himself but stated his legs felt heavy. At 1:50 pm the CNA answered his call light and found he had taken himself to the bathroom. She stated that when he went to get back into the bed it was ""abnormal"" how he was getting into it so she assisted him. At that time he quit breathing and she called a RN into the room immediately. He was found without a pulse, respirations, or blood pressure at 1:54 pm. He was a DNR."

 

Patient Age	93.00	Sex	Male
State / Territory	South Dakota	Date Report Completed	2021-01-05
Date Vaccinated	2021-01-04	Date Report Received	2021-01-05
Date of Onset	2021-01-04	Date Died	2021-01-04
Days to onset	0
Vaccine Administered By	Senior Living *	Vaccine Purchased By	Not Applicable *
Mfr/Imm Project Number	NONE	Report Form Version	2
Recovered	No	Serious	Yes

 

 

Vaccine Type	Vaccine	Manufacturer	Lot	Dose	Route	Site
COVID19 VACCINE	COVID19 (COVID19 (PFIZER-BIONTECH))	PFIZER\BIONTECH	EL0140	1	IM	LA

 

Medications At Time Of Vaccination

History/Allergies

Ferrex 150 mg, Folic Acid 1 mg, Furosemide 20 mg, Isosorbide Mononoitrate ER 30 mg, Lactulose 15 mL, Omeprazole 40 mg, Potassium Chloride ER 20 MEQ, Metoprolol 12.5 mg, PreserVision AREDS 2 one capsule, Ranolazine ER 1,000 mg, and Sucralf

ACUTE POSTHEMORRHAGIC ANEMIA, ATHEROSCLEROTIC HEART DISEASE OF NATIVE CORONARY ARTERY WITH OTHER FORMS OF ANGINA PECTORIS, CARDIAC MURMUR, UNSPECIFIED, CHRONIC KIDNEY DISEASE, STAGE 2, CHRONIC OBSTRUCTIVE PULMONARY DISEASE, EMPHYSEMA, ESSENTIAL (PRIMARY) HYPERTENSION, FRACTURE OF NASAL BONES, INITIAL ENCOUNTER FOR CLOSED FRACTURE, HYPOXEMIA, PAROXYSMAL ATRIAL FIBRILLATION, PRESENCE OF CARDIAC PACEMAKER, THROMBOCYTOPENIA, UNSPECIFIED CIRRHOSIS OF LIVER, and UNSPECIFIED DIASTOLIC (CONGESTIVE) HEART FAILURE.,NKA