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Reporte zur Charge EW6204

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

9Reporte angezeigt
0Todesfaelle
2Hospitalisiert
2Lebensbedrohlich
0Bleibende Schaeden
AZ 1 IN 1 CO 1 OH 1 OR 1 TN 1 GA 1 IL 1

VAERS 1140394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW6204

kritisch
Staat
AZ
Alter
69,0
Geschlecht
F
Eingang
27.03.2021
Impfdatum
25.02.2021
Beginn
24.03.2021
Tage bis Beginn
27,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Acute respiratory failure Anion gap normal Arthralgia Basophil count decreased Basophil percentage decreased Blood calcium normal Blood chloride decreased Blood creatinine normal Blood glucose normal Blood lactic acid normal Blood magnesium increased Blood potassium normal Blood sodium decreased Blood urea decreased Breath sounds abnormal Cough Dyspnoea Dyspnoea exertional

Symptomtext

This is a 70 year old female with paroxysmal atrial fibrillation (anticoagualted on Eliquis), obstructive sleep apnea (uses CPAP), mitral valve regurgitation, remote tobacco use, hypertension and dyslipidemia who presents to the ED for worsening dyspnea, cough, subjective fever, chills and body aches that have been ongoing for the past several days. The patient indicates that her dyspnea is exacerbated with exertion but she denies chest pain, pleuritic chest pain, leg swelling or calf pain. She mentions that she has received both of her COVID-19 vaccines (Pfizer); the first immunization was on 02/25 followed by her second immunization which took place eight days ago on 03/18. She is not confident that she has had any contact with a known sick or definitive COVID-positive individual recently. Of note, the last documented incidence of testing for COVID-19 was performed on 10/31/2020 after the patient was seen at a Clinic after a exposure for a COVID-positive individual. Testing at that time had resulted negative. To her knowledge, she states that she had, in fact, tested positive for COVID-19 in late fall of 2020, but she was not hospitalized. Yesterday (3/26/2021), she was evaluated at a Pharmacy where she was testing for COVID-19 which has since resulted positive. The patient denies any other acute symptoms of illness. In the ED, the patient was found to have acute respiratory failure with hypoxemia and pneumonia due to SARS-CoV-2 infection. Review of Systems Constitutional: Positive for chills, fatigue and fever. Negative for activity change. Respiratory: Positive for cough and shortness of breath. Cardiovascular: Negative for chest pain and leg swelling. Gastrointestinal: Negative for abdominal pain, diarrhea, nausea and vomiting. Genitourinary: Negative for dysuria. Musculoskeletal: Positive for arthralgias and myalgias. Negative for gait problem. Neurological: Negative for syncope. All other systems reviewed and are negative. Vitals Blood pressure 159/79, pulse 65, temperature 36.4 ?C (97.5 ?F), temperature source Oral, resp. rate 18, height 1.6 m (5' 3"), weight 107 kg, SpO2 98 %. Physical Exam Vitals reviewed. Constitutional: General: She is awake. She is not in acute distress. Appearance: Normal appearance. She is well-developed. She is morbidly obese. She is ill-appearing. She is not toxic-appearing. Interventions: Nasal cannula in place. HENT: Head: Normocephalic and atraumatic. Nose: Congestion present. Mouth/Throat: Mouth: Mucous membranes are dry. Pharynx: Oropharynx is clear. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulses: Normal pulses. Heart sounds: Normal heart sounds. Pulmonary: Effort: Pulmonary effort is normal. Breath sounds: Decreased breath sounds present. Comments: Diminished breath sounds in all lung fields. Occasional cough. Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: General: Normal range of motion. Cervical back: Normal range of motion and neck supple. Skin: General: Skin is warm and dry. Neurological: General: No focal deficit present. Mental Status: She is alert and oriented to person, place, and time. Psychiatric: Behavior: Behavior is cooperative.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
2,0
Labordaten
Diagnostic Results LABS Recent Results (from the past 24 hour(s)) Basic Metabolic Panel Collection Time: 03/26/21 7:52 PM Result Value Ref Range Glucose 163 (H) 70 - 99 mg/dL Urea Nitrogen (BUN) 9 8 - 23 mg/dL Creatinine 0.8 0.5 - 0.9 mg/dL Calcium (Ca) 9.3 8.8 - 10.2 mg/dL Sodium (Na) 131 (L) 136 - 145 mmol/L Potassium (K) 4.0 3.4 - 5.1 mmol/L Chloride (Cl) 92 (L) 98 - 107 mmol/L Carbon Dioxide (CO2) 25 22 - 29 mmol/L Anion Gap 14 (H) 3 - 11 mEq/L CBC with Auto Differential Collection Time: 03/26/21 7:52 PM Result Value Ref Range WBC 5.7 4.0 - 11.0 X1000/UL RBC 4.83 4.20 - 5.40 M/UL HGB 15.1 12.0 - 16.0 g/dL HCT 43.4 35.0 - 50.0 % MCV 89.8 80.0 - 100.0 FL MCH 31.2 (H) 27.0 - 31.0 PG MCHC 34.7 32.0 - 36.0 G/DL RDW 13.1 11.5 - 14.5 % Platelet Count 121 (L) 130 - 450 K/UL MPV 7.9 7.4 - 10.4 FL Neutrophils, auto 87.0 (H) 54 - 62 % Lymphocytes, auto 9.1 (L) 25 - 35 % Monocytes, auto 3.6 (L) 5.5 - 11.7 % Eosinophils, auto 0.0 0 - 5 % Basophils, auto 0.3 0 - 2.9 % Absolute Lymphocytes 0.5 (L) 1.0 - 3.2 K/uL Absolute Monocytes 0.2 (L) 0.3 - 1.1 K/uL Absolute Neutrophils 5.0 1.7 - 7.6 K/uL Absolute Eosinophils 0.0 0.0 - 0.5 K/uL Absolute Basophils 0.0 0.0 - 0.1 K/uL Troponin T Collection Time: 03/26/21 7:52 PM Result Value Ref Range TROPONIN T <0.01 0.00 - 0.01 ng/mL Troponin Note See Comment Lactic Acid Collection Time: 03/26/21 7:52 PM Result Value Ref Range LACTIC ACID 1.9 0.5 - 2.2 mmol/L Magnesium Collection Time: 03/26/21 7:52 PM Result Value Ref Range Magnesium 2.4 1.6 - 2.4 mg/dL PT/INR Collection Time: 03/26/21 7:52 PM Result Value Ref Range PT 20.3 (H) 9.4 - 12.6 SEC INR 1.74 (H) 0.90 - 1.20 Procalcitonin Collection Time: 03/26/21 7:52 PM Result Value Ref Range Procalcitonin 0.09 0.00 - 0.50 ng/mL Procalcitonin Note See Comment Note TMC Lab COVID-19 (In-house) Collection Time: 03/26/21 7:55 PM Specimen: Nasopharyngeal ; SWAB Result Value Ref Range COVID Source Nasopharyngeal swab SARS-CoV-2 (COVID-19) Positive (A) NEG Previously tested for COVID-19 Y Employed in healthcare Unknown COVID-19 Symptomatic as defined by CDC Y Date of Symptom Onset 20,210,326 Hospitalized for COVID-19 N Admitted to ICU for COVID-19 N Resident in a congregate care setting Unknown Is Patient Pregnant? Not Pregnant Respiratory Panel By PCR Collection Time: 03/26/21 8:46 PM Result Value Ref Range Resp Spec Source Nasopharyngeal swab Resp Panel Results No Organisms Detected Resp Panel Comment See Comment IMAGING ? Chest 1 view Portable, 3/26/2021 Poor inspiratory effort. Bilateral multifocal infiltrate. CARDIAC ? EKG 12 Lead, 3/26/2021 @ 16:01 Sinus rhythm at a rate of 76 bpm. Baseline wander in lead(s) II, III, aVF.
Aktuelle Erkrankungen
No other acute illnesses known at the time of vaccinations.
Vorgeschichte
OSA on CPAP Class 3 severe obesity in adult (HCC) Atrial fibrillation (HCC) Essential hypertension Dyslipidemia
Andere Medikamente
Albuterol Sulfate (ALBUTEROL, USE PROVENTIL HFA,) 90 MCG/ACT Inhale 1-2 puffs into the lungs every four hours as needed amiodarone (PACERONE) 200 MG tablet Take 200 mg by mouth daily. apixaban (ELIQUIS) 5 MG tablet Take 5 mg by mouth tw
Allergien
Morphine (nausea/vomiting)
Vorherige Impfungen
-

VAERS 1191883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW6204

schwer
Staat
IN
Alter
55,0
Geschlecht
F
Eingang
13.07.2021
Impfdatum
25.03.2021
Beginn
26.03.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Fatigue Headache Nausea Syncope

Symptomtext

Severe Nausea; Extreme joint pain; Headache; fatigue; This is a spontaneous report from a contactable consumer, the patient. A 55-year-old non-pregnant female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EW6204) via an unspecified route of administration on 25Mar2021 at 14:00 (at the age of vaccination 55-years-old) in the right arm as a single dose for COVID-19 immunisation. Medical history included barrettes oesophagus. The patient did not have a history of allergies to medications, food, or other products. Concomitant medications included spironolactone (MANUFACTURER UNKNOWN) for unknown indication, estradiol (ESTROGEN) for unknown indication, progesterone (MANUFACTURER UNKNOWN) for unknown indication, esomeprazole magnesium (NEXIUM) for unknown indication which were received within two weeks of vaccination. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EN6198) via an unspecified route of administration in the right arm on 04Mar2021 at 14:00 (at the age of vaccination 55-years-old) as a single dose for COVID-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 26Mar2021 at 02:00, the patient had experienced severe nausea, extreme joint pain, headache and fatigue. The patient did not receive any treatment for the reported events. Adverse events did not result in a visit to the doctors or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The clinical outcome of the events severe nausea, extreme joint pain, headache and fatigue was resolved in Mar2021 at the time of report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Barrett's esophagus (Barrettes esophagus)
Andere Medikamente
ESTROGEN; PROGESTERONE; SPIRONOLACTONE; Nexium
Allergien
-
Vorherige Impfungen
-

VAERS 1450206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW6204

moderat
Staat
CO
Alter
60,0
Geschlecht
F
Eingang
06.07.2021
Impfdatum
26.03.2021
Beginn
29.03.2021
Tage bis Beginn
3,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chest discomfort Computerised tomogram normal Dyspnoea Electrocardiogram normal Fatigue Headache Laboratory test normal

Symptomtext

Woke up three days after the vaccination with sever fatigue, shortness of breath, and a severe headache. Fiance rushed me to the ER because I couldn't catch my breath. All tests came back negative/normal. CT scan didn't show any pulmonary embolism which they thought I had. They released me. The symptoms have continued and have gotten worse. I now have tightening around the heart and lungs along with headaches on a daily basis. When I get those "attacks" it can drop me to my knees. Am currently looking to follow up with a cardiologist.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
ECG, CT Scan, blood work
Aktuelle Erkrankungen
None
Vorgeschichte
Possible high cholesterol - not high enough I have to be on meds but drs always tell me I have
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1391654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew6204

moderat
Staat
OH
Alter
57,0
Geschlecht
F
Eingang
11.06.2021
Impfdatum
26.04.2021
Beginn
17.05.2021
Tage bis Beginn
21,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Abdominal pain upper Anaemia Autoimmune hepatitis Biopsy bone marrow abnormal Chest X-ray Chills Computerised tomogram abdomen abnormal Echocardiogram abnormal Electrocardiogram abnormal Fatigue Hepatomegaly Laboratory test abnormal Malaise Pain Pyrexia Sinus bradycardia Splenic infarction Splenomegaly

Symptomtext

Patient developed low grade fever, chills, body aching, RUQ pain, malaise, fatigue on 5/17/21. Saw PCP on 5/21/21 found to be anemic, went to ER and was admitted on 5/22/21. Splenic infarcts, Splenomegaly, and Hepatomegaly. Diagnosed with autoimmune Hepatitis after multiple tests such as bone marrow biopsies, CT scans, and labs. She also developed sinus bradycardia pauses and bouts of SVT.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Supraventricular tachycardia
Hospital-Tage
13,0
Labordaten
CT abd 5/22/21, US abd 5/22/21, chest xray 5/22/21, EKG 5/22/21, Echocardiogram 5/23/21 bone marrow bx 6/2/21.
Aktuelle Erkrankungen
None
Vorgeschichte
HTN, DM type II, metabolic syndrome, hyperlipidemia, osteoarthritis,
Andere Medikamente
Aspirin 81 mg daily, atorvastatin 10 mg daily, vitamin D 50,000 unit capsule weekly, metformin 500 mg BID, meloxicam 15 mg daily, atenolol 25 mg daily
Allergien
Augmentin
Vorherige Impfungen
-

VAERS 2311691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW6204

mild
Staat
OR
Alter
72,0
Geschlecht
M
Eingang
07.06.2022
Impfdatum
23.02.2021
Beginn
01.03.2021
Tage bis Beginn
6,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Joint swelling Musculoskeletal stiffness Restless legs syndrome

Symptomtext

After his booster on 2/23/21 he had joint pain that made it hard to work and swelling behind the left knee. It was so stiff he could not bend his leg. Also restless leg.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
CVID, primary IgA deficiency, hashimoto's thyroiditis, ADHD
Andere Medikamente
lisinopril, testosterone, gabapentin, tamsulosin, furosemide, metoprolol, levothyroxine, IVIG
Allergien
Amoxicillin, augmentin, oflxacin
Vorherige Impfungen
-

VAERS 1776933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW6204

mild
Staat
-
Alter
42,0
Geschlecht
F
Eingang
11.10.2021
Impfdatum
24.03.2021
Beginn
18.09.2021
Tage bis Beginn
178,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Ageusia Anosmia Headache Respiratory tract congestion Rhinorrhoea

Symptomtext

runny nose, loss of taste and smell, headache, congestion

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1534381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW6204

mild
Staat
TN
Alter
66,0
Geschlecht
F
Eingang
07.08.2021
Impfdatum
02.03.2021
Beginn
02.03.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fatigue Headache Myalgia Nausea Vaccination site pain Vaccination site swelling

Symptomtext

Injection site pain; Tiredness/ feeling extremely tired; Headache; Muscle pain; Injection site swelling; Nausea; This is a spontaneous report from a contactable consumer, the patient. A 66-year-old non-pregnant female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW6204) via an unspecified route of administration in the left arm on 02Mar2021 at 09:00 (at the age of 66-years-old) as a single dose for COVID-19 immunisation. Medical history included diabetes II, high cholesterol, Obese, HBP (blood pressure high) and COVID-19 (Prior to the vaccination, the patient was diagnosed with COVID-19). The patient received doxycycline (MANUFACTURER UNKNOWN) and metaxalone (SKELAXIN) on unknown date for an unspecified indication and experienced drug allergy. The patient received unspecified medication within two weeks of vaccination. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. On 02Mar2021 at 09:00, the patient experienced injection site pain, tiredness, headache, muscle pain, injection site swelling, nausea and feeling extremely tired. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. No therapeutic measures were taken as a result of the reported event. The clinical outcomes of injection site pain, tiredness, headache, muscle pain, injection site swelling, nausea and feeling extremely tired were recovered on an unknown date in 2021. The patient also received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0151) via an unspecified route of administration in the left arm on 06Apr2021 as a single dose for COVID-19 immunisation. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood pressure high (HBP); COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?:Yes); High cholesterol; Obesity (Obese); Type II diabetes mellitus (Diabetes II)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1392925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew6204

mild
Staat
GA
Alter
72,0
Geschlecht
F
Eingang
11.06.2021
Impfdatum
23.03.2021
Beginn
24.03.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood test normal Fatigue Loss of personal independence in daily activities

Symptomtext

Patient has experienced extreme fatigue limiting daily routines such as shopping, talking care of her house, cooking and even walking since getting the last vaccine approximately 3 months ago.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
Patient stated md had ran blood work that all came back normal.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1424878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW6204

gering
Staat
IL
Alter
37,0
Geschlecht
F
Eingang
24.06.2021
Impfdatum
18.05.2021
Beginn
18.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Vaccine positive rechallenge

Symptomtext

Muscle spasms/twitching in right arm evening of first dose. Muscle twitching/spasm in left arm evening of second dose. Narcolepsy symptom of daytime sleepiness exasperated since vaccination ?worse since receiving second dose, but somewhat worse after first dose. Has persisted and is worse than prior to receiving vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vaccine positive rechallenge
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Narcolepsy Type 1
Andere Medikamente
Provigil 200mg
Allergien
None
Vorherige Impfungen
-