Received Apr 28, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 2 | EW0151 | — |
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 2 | EW0151 | — |
coma; Sepsis; shaky leg syndrome; lost lot of her memory; Could not walk; Had partial hysterectomy for fibroids; written allergic reaction; said diarrhea, did not have diarrhea, had constipation; Said vomiting, was sent home; got really sick; Had rash and other signs and symptoms; This is a spontaneous report received from a Consumer or other non HCP, Program ID. A 52-year-old female patient received BNT162b2 (COMIRNATY), on 10Apr2021 as dose 2, single (Lot number: EW0151) at the age of 52 years, in arm for covid-19 immunisation. The patient had no relevant medical history. The patient took concomitant medications (They had her on so many medications, in hospital, wants to say, like 30 pills, like 60 pills a day. Did not need anything but antibiotics and IV hydration. They did not have her on any of that. They had her on sedation medication, anxiety medication, sleeping, sedation. There were things she should not have been on). Vaccination history included: comirnaty (DOSE 1, Lot number EP6955), administration date: 20Mar2021, when the patient was 52-year-old, for COVID-19 immunization, reaction(s): "cough". The following information was reported: RASH (non-serious) with onset Nov2021, outcome "unknown", described as "Had rash and other signs and symptoms"; ILLNESS (non-serious) with onset 21Nov2021, outcome "unknown", described as "got really sick"; VOMITING (non-serious) with onset 29Nov2021, outcome "unknown", described as "Said vomiting, was sent home"; CONSTIPATION (non-serious) with onset 29Nov2021, outcome "unknown", described as "said diarrhea, did not have diarrhea, had constipation"; HYPERSENSITIVITY (non-serious) with onset 29Nov2021, outcome "unknown", described as "written allergic reaction"; SEPSIS (hospitalization) with onset 30Nov2021, outcome "not recovered"; COMA (hospitalization, medically significant) with onset 30Nov2021, outcome "recovered"; UTERINE LEIOMYOMA (medically significant), outcome "unknown", described as "Had partial hysterectomy for fibroids"; RESTLESS LEGS SYNDROME (non-serious), outcome "unknown", described as "shaky leg syndrome"; AMNESIA (non-serious), outcome "unknown", described as "lost lot of her memory"; GAIT INABILITY (non-serious), outcome "unknown", described as "Could not walk". The patient was hospitalized for coma, sepsis (start date: 30Nov2021, hospitalization duration: 30 day(s)). The event "had partial hysterectomy for fibroids" required physician office visit. The events "coma" and "sepsis" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Blood test: (2021) not call it sepsis, notes: Woke up a few days later, they were denying it was sepsis, would not call it sepsis, blood test proved it; Sepsis: (unspecified date) 4.27, notes: had 4.27 sepsis detection score; (2021) 1.9, notes: positive test was sepsis, with detection score 1.9; Lymph nodes scan normal: (2021) negative, notes: lymph node tests negative; Viral test: (2021) Negative, notes: switched to viral encephalitis, test was negative; West Nile virus test: (2021) negative, notes: West Nile test was negative; Body temperature: (2021) 104 degree. Therapeutic measures were taken as a result of uterine leiomyoma, sepsis. Clinical course: The patient was no allergic to any previous vaccination, medications, food or other products. The patient did not receive any other vaccines on the same date as the Pfizer vaccine. The patient did not receive any other vaccines within 4 weeks prior to the first administration of the suspect vaccine. Kept telling her it was West Nile virus, shaky leg syndrome. Could not walk, lost lot of her memory. West Nile test was negative, then switched to viral encephalitis, test was negative. Tried to blame UTI, those tests, lymph node tests negative. Only positive test was sepsis, with detection score 1.9. Friend went with he to ER, was told to immediately come right back. Now, had 4.27 sepsis detection score, was in coma. Doctor put her on amoxicillin, numbers started to come back down to 1.9. Woke up, hospital risk management was there. All 4 doctors claimed, it was West Nile Virus, took her off antibiotics, kept telling her it was mosquito bite. They ran 3 tests back to back, were negative. Was seizing every 7 seconds. Sister was forced to sign paper, stating, if she did not allow them to do spinal tap, caller would die. Clarified, she was admitted to hospital, with sepsis and got Covid-19 booster, while in hospital, had severe reaction after booster. Had to do those injections for work, is medic. Clarified, caller hospitalized 30Nov2021, with sepsis, received Covid-19 booster, 21Dec2021. Had partial hysterectomy for fibroids, for in and out procedure, Friday, 19Nov2021. Started reaching out to doctor, 2 days after, got really sick. Had rash and other signs and symptoms. 29Nov2021, her nurse reached out, said to get to nearted ER. Blood work was showing sepsis, they told her she was fine, said it was allergic reaction. For paperwork they had written allergic reaction, said diarrhea, did not have diarrhea, had constipation. Said vomiting, was sent home. Then, next day, went in coma, brought right back to same hospital, 30Nov2021. Clarified, caller in hospital, total 30 days, after being brought in, admitted, 30Nov2021, with coma. Woke up either third day or fourth day, family was with her in hospital. Was sedated, 3 people held her down, nurse falsified questionnaire. Came in 30Nov2021, with 104 degree temperature, she marked no. Asked if temperature over 100 degrees, within last 30 days, typed no, they falsified document. Believes nurse who administered Covid shot, falsified documentation. Should have never had shot, was contraindicated, should never have happened. Had been doing plasma injections by Pfizer, Hemoglobin IVG( Pangyza).; Sender's Comments: Linked Report(s) : US-PFIZER INC-202500086583 same patient/drug, different events(LOE);US-PFIZER INC-202500087098 same patient/drug, different vaccine dose/ events;US-PFIZER INC-202500087099 same patient/drug, different vaccine dose/ events;
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Test Date: 2021; Test Name: blood test; Result Unstructured Data: Test Result:not call it sepsis; Comments: Woke up a few days later, they were denying it was sepsis, would not call it sepsis, blood test proved it.; Test Name: Sepsis; Result Unstructured Data: Test Result:4.27; Comments: had 4.27 sepsis detection score; Test Date: 2021; Test Name: Sepsis; Result Unstructured Data: Test Result:1.9; Comments: positive test was sepsis, with detection score 1.9.; Test Date: 2021; Test Name: lymph node tests; Test Result: Negative ; Comments: lymph node tests negative.; Test Date: 2021; Test Name: viral encephalitis; Test Result: Negative ; Comments: switched to viral encephalitis, test was negative; Test Date: 2021; Test Name: West Nile test; Test Result: Negative ; Comments: West Nile test was negative; Test Date: 2021; Test Name: temperature; Result Unstructured Data: Test Result:104 degree