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Reporte zur Charge FJ6796

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

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2Hospitalisiert
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IN 2

VAERS 2563520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6796

mild
Staat
IN
Alter
76,0
Geschlecht
F
Eingang
01.02.2023
Impfdatum
28.12.2022
Beginn
28.12.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Aphasia Blood creatine phosphokinase C-reactive protein Culture urine Differential white blood cell count Chills Dizziness Fall Full blood count International normalised ratio Metabolic function test Red blood cell sedimentation rate Gait inability Investigation Protein total Urine analysis

Symptomtext

collapsed to the floor; unable to walk; Dizziness; severe chilling; The initial case was missing the following minimum criteria: Unspecified AE. Upon receipt of follow-up information on 25Jan2023, this case now contains all required information to be considered valid. This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 76-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Dec2022 at 12:15 as dose 4 (booster), single (Lot number: FJ6796, Expiration Date: 31Jan2024) at the age of 76 years, in left arm for covid-19 immunization. The patient's relevant medical history included: "Polymyalgia rheumatica", start date: Jan2017 (ongoing), notes: Polymyalgia rheumatica; "Allergies" (ongoing); "Cholesterol" (ongoing); "Blood clots" (ongoing); "B/P" (ongoing). Concomitant medication(s) included: LISINOPRIL taken for blood pressure measurement (ongoing); WARFARIN taken for thrombosis, start date: Aug2019 (ongoing); ATORVASTATIN taken for blood cholesterol (ongoing); MONTELUKAST [MONTELUKAST SODIUM] taken for hypersensitivity (ongoing). Vaccination history included: BNT162b2 (Dose: 1st, Time: 10:57 am, Site and Route of injection: Left Arm, Batch/Lot number: EM9810), administration date: 11Feb2021, when the patient was 74-year-old, for COVID-19 immunization; BNT162b2 (Dose: 2nd, Time: 10:44 am, Site and Route of injection: Left Arm, Batch/Lot number: EN6200), administration date: 04Mar2021, when the patient was 74-year-old, for COVID-19 immunization; BNT162b2 (Dose: 3rd, Time: 12 noon, Site and Route of injection: Left Arm, Batch/Lot number: FC3184), administration date: 01Oct2021, when the patient was 75-year-old, for COVID-19 Immunization. The following information was reported: DIZZINESS (hospitalization) with onset 28Dec2022 at 20:15, outcome "recovered"; CHILLS (hospitalization) with onset 28Dec2022 at 20:15, outcome "recovered", described as "severe chilling"; GAIT INABILITY (hospitalization) with onset 29Dec2022, outcome "recovered", described as "unable to walk"; FALL (hospitalization) with onset 29Dec2022 at 02:00, outcome "recovered", described as "collapsed to the floor". The patient was hospitalized for fall, chills, gait inability, dizziness (discharge date: 31Dec2022, hospitalization duration: 3 day(s)). The events "collapsed to the floor", "severe chilling", "unable to walk" and "dizziness" required emergency room visit. The patient underwent the following laboratory tests and procedures: Blood creatine phosphokinase: (29Dec2022) 56, notes: Unit: u/L; C-reactive protein: (29Dec2022) 65.5 mg/l; Full blood count: (29Dec2022) Unknown results; I had lab work: (unspecified date) Unknown results, notes: Lab Test (Within two weeks): Consumer stated, "Yes, when I was in the hospital yes, I had lab work."; Metabolic function test: (29Dec2022) Unknown results; Protein total: (29Dec2022) 2.2; Red blood cell sedimentation rate: (29Dec2022) 20, notes: unit: mm/He; Urine analysis: (29Dec2022) Unknown results. Therapeutic measures were not taken as a result of fall, chills, gait inability, dizziness. Clinical course: Vaccine facility type: Pharmacy or Drug store (4rth dose booster), Vaccine facility type: Pharmacy or Drug store (3rd dose booster), Vaccine facility type: Hospital (2nd dose), Vaccine facility type: Hospital (1st dose). I have had a reaction (Further not specified the reaction, hence event captured as per the verbatim) to the two Pfizer booster (Suspect clarified as Pfizer COVID-19 Vaccine), and I did not report the first one which was in Oct2021 but I was hospitalized for three days this time (Further hospitalization details were not available over the call, hence event captured as per the verbatim) after getting the newest booster and I thought somebody needed to know this." Vaccine at 12:15 pm 28Dec2022. Severe chilling and Dizziness at 8:15 pm. Wake up my husband around 2 am, 29Dec2022 standing beside bed, told him and was "going down" and collapse to the floor. I was unable to walk without assistance. My husband took me to the E.R, I was admitted. Dismissed around 8:00 pm on 31Dec2022. Onset time: 8:15 pm, Seriousness Criteria: If hospitalization, duration of stay: 3 day Treatment: No. Reporter information: Other, please specify: Self

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
3,0
Labordaten
Test Date: 20221229; Test Name: CK; Result Unstructured Data: Test Result:56; Comments: Unit: u/L; Test Date: 20221229; Test Name: C-Reactive protein; Result Unstructured Data: Test Result:65.5 mg/l; Test Date: 20221229; Test Name: CBC panel w/diff; Result Unstructured Data: Test Result:Unknown results; Test Name: I had lab work; Result Unstructured Data: Test Result:Unknown results; Comments: Lab Test (Within two weeks): Consumer stated, "Yes, when I was in the hospital yes, I had lab work."; Test Date: 20221229; Test Name: Comp metabolic; Result Unstructured Data: Test Result:Unknown results; Test Date: 20221229; Test Name: Protein-INR; Result Unstructured Data: Test Result:2.2; Test Date: 20221229; Test Name: Sed rate; Result Unstructured Data: Test Result:20; Comments: unit: mm/He; Test Date: 20221229; Test Name: Urinalysis; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen
Allergy; Blood pressure; Cholesterol; Clot blood; Polymyalgia rheumatica (Polymyalgia rheumatica)
Vorgeschichte
-
Andere Medikamente
LISINOPRIL; WARFARIN; ATORVASTATIN; MONTELUKAST [MONTELUKAST SODIUM]
Allergien
-
Vorherige Impfungen
-

VAERS 2563520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FJ6796

mild
Staat
IN
Alter
76,0
Geschlecht
F
Eingang
01.02.2023
Impfdatum
28.12.2022
Beginn
28.12.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Aphasia Blood creatine phosphokinase C-reactive protein Culture urine Differential white blood cell count Chills Dizziness Fall Full blood count International normalised ratio Metabolic function test Red blood cell sedimentation rate Gait inability Investigation Protein total Urine analysis

Symptomtext

collapsed to the floor; unable to walk; Dizziness; severe chilling; The initial case was missing the following minimum criteria: Unspecified AE. Upon receipt of follow-up information on 25Jan2023, this case now contains all required information to be considered valid. This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 76-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Dec2022 at 12:15 as dose 4 (booster), single (Lot number: FJ6796, Expiration Date: 31Jan2024) at the age of 76 years, in left arm for covid-19 immunization. The patient's relevant medical history included: "Polymyalgia rheumatica", start date: Jan2017 (ongoing), notes: Polymyalgia rheumatica; "Allergies" (ongoing); "Cholesterol" (ongoing); "Blood clots" (ongoing); "B/P" (ongoing). Concomitant medication(s) included: LISINOPRIL taken for blood pressure measurement (ongoing); WARFARIN taken for thrombosis, start date: Aug2019 (ongoing); ATORVASTATIN taken for blood cholesterol (ongoing); MONTELUKAST [MONTELUKAST SODIUM] taken for hypersensitivity (ongoing). Vaccination history included: BNT162b2 (Dose: 1st, Time: 10:57 am, Site and Route of injection: Left Arm, Batch/Lot number: EM9810), administration date: 11Feb2021, when the patient was 74-year-old, for COVID-19 immunization; BNT162b2 (Dose: 2nd, Time: 10:44 am, Site and Route of injection: Left Arm, Batch/Lot number: EN6200), administration date: 04Mar2021, when the patient was 74-year-old, for COVID-19 immunization; BNT162b2 (Dose: 3rd, Time: 12 noon, Site and Route of injection: Left Arm, Batch/Lot number: FC3184), administration date: 01Oct2021, when the patient was 75-year-old, for COVID-19 Immunization. The following information was reported: DIZZINESS (hospitalization) with onset 28Dec2022 at 20:15, outcome "recovered"; CHILLS (hospitalization) with onset 28Dec2022 at 20:15, outcome "recovered", described as "severe chilling"; GAIT INABILITY (hospitalization) with onset 29Dec2022, outcome "recovered", described as "unable to walk"; FALL (hospitalization) with onset 29Dec2022 at 02:00, outcome "recovered", described as "collapsed to the floor". The patient was hospitalized for fall, chills, gait inability, dizziness (discharge date: 31Dec2022, hospitalization duration: 3 day(s)). The events "collapsed to the floor", "severe chilling", "unable to walk" and "dizziness" required emergency room visit. The patient underwent the following laboratory tests and procedures: Blood creatine phosphokinase: (29Dec2022) 56, notes: Unit: u/L; C-reactive protein: (29Dec2022) 65.5 mg/l; Full blood count: (29Dec2022) Unknown results; I had lab work: (unspecified date) Unknown results, notes: Lab Test (Within two weeks): Consumer stated, "Yes, when I was in the hospital yes, I had lab work."; Metabolic function test: (29Dec2022) Unknown results; Protein total: (29Dec2022) 2.2; Red blood cell sedimentation rate: (29Dec2022) 20, notes: unit: mm/He; Urine analysis: (29Dec2022) Unknown results. Therapeutic measures were not taken as a result of fall, chills, gait inability, dizziness. Clinical course: Vaccine facility type: Pharmacy or Drug store (4rth dose booster), Vaccine facility type: Pharmacy or Drug store (3rd dose booster), Vaccine facility type: Hospital (2nd dose), Vaccine facility type: Hospital (1st dose). I have had a reaction (Further not specified the reaction, hence event captured as per the verbatim) to the two Pfizer booster (Suspect clarified as Pfizer COVID-19 Vaccine), and I did not report the first one which was in Oct2021 but I was hospitalized for three days this time (Further hospitalization details were not available over the call, hence event captured as per the verbatim) after getting the newest booster and I thought somebody needed to know this." Vaccine at 12:15 pm 28Dec2022. Severe chilling and Dizziness at 8:15 pm. Wake up my husband around 2 am, 29Dec2022 standing beside bed, told him and was "going down" and collapse to the floor. I was unable to walk without assistance. My husband took me to the E.R, I was admitted. Dismissed around 8:00 pm on 31Dec2022. Onset time: 8:15 pm, Seriousness Criteria: If hospitalization, duration of stay: 3 day Treatment: No. Reporter information: Other, please specify: Self

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
3,0
Labordaten
Test Date: 20221229; Test Name: CK; Result Unstructured Data: Test Result:56; Comments: Unit: u/L; Test Date: 20221229; Test Name: C-Reactive protein; Result Unstructured Data: Test Result:65.5 mg/l; Test Date: 20221229; Test Name: CBC panel w/diff; Result Unstructured Data: Test Result:Unknown results; Test Name: I had lab work; Result Unstructured Data: Test Result:Unknown results; Comments: Lab Test (Within two weeks): Consumer stated, "Yes, when I was in the hospital yes, I had lab work."; Test Date: 20221229; Test Name: Comp metabolic; Result Unstructured Data: Test Result:Unknown results; Test Date: 20221229; Test Name: Protein-INR; Result Unstructured Data: Test Result:2.2; Test Date: 20221229; Test Name: Sed rate; Result Unstructured Data: Test Result:20; Comments: unit: mm/He; Test Date: 20221229; Test Name: Urinalysis; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen
Allergy; Blood pressure; Cholesterol; Clot blood; Polymyalgia rheumatica (Polymyalgia rheumatica)
Vorgeschichte
-
Andere Medikamente
LISINOPRIL; WARFARIN; ATORVASTATIN; MONTELUKAST [MONTELUKAST SODIUM]
Allergien
-
Vorherige Impfungen
-