- Staat
- MI
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 29.10.2023
- Impfdatum
- 19.01.2022
- Beginn
- 26.07.2023
- Tage bis Beginn
- 553,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Cerebrovascular accident
Computerised tomogram
Dysarthria
Echocardiogram
Facial paralysis
Hypoaesthesia
Magnetic resonance imaging
Ultrasound Doppler
Symptomtext
Stroke Left side numbness, slurred speech, drooping face TPA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 4,0
- Labordaten
- Mri, ct scans, echocardiogram, tte, doplar of arms & legs
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 13.09.2023
- Impfdatum
- 06.01.2022
- Beginn
- 24.05.2023
- Tage bis Beginn
- 503,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Hepatorenal syndrome
Hypotension
Symptomtext
I95.9 HYPOTENSION 5/23/2023 HEPATORENAL SYNDROME J96.00 ACUTE RESPIRATORY FAILURE 5/24/2023 HEPATORENAL SYNDROME
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 07.06.2023
- Impfdatum
- 14.05.2021
- Beginn
- 02.07.2022
- Tage bis Beginn
- 414,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute sinusitis
Agitation
Agonal respiration
Angiogram cerebral abnormal
Angiogram pulmonary abnormal
Angiogram
Angiogram cerebral
Angiogram pulmonary
Antibody test
Antibody test positive
Arteriosclerosis coronary artery
Biopsy bone marrow
Blood pressure increased
Blood sodium decreased
Blood pressure measurement
Blood sodium
Blood test
Bronchiolitis
Symptomtext
Death; BLOOD SODIUM DECREASED; Arteriosclerosis coronary artery; HYPOTHERMIA; Agonal respiration; Bronchiolitis; URETHRAL HAEMORRHAGE; Cardio-respiratory arrest; AGITATION; Encephalopathy; BRONCHITIS; Hypothermia; HAEMOFILTRATION; Respiratory arrest; MUCOSAL HYPERTROPHY; Seizure like phenomena; PERIPHERAL ISCHAEMIA; Thrombosis; RED BLOOD CELL TRANSFUSION; Unresponsive to stimuli; SARS-COV-2 TEST POSITIVE; Urethral haemorrhage; SECRETION DISCHARGE; Ventricular dyssynchrony; VACCINE BREAKTHROUGH INFECTION; Acute sinusitis; DEATH; Agitation; ARTERIOSCLEROSIS CORONARY ARTERY; Angiogram cerebral abnormal; BRONCHIOLITIS; Angiogram pulmonary abnormal; CARDIO-RESPIRATORY ARREST; Antibody test positive; ENCEPHALOPATHY; Biopsy bone marrow; RESPIRATORY ARREST; Blood pressure increased; SEIZURE LIKE PHENOMENA; Blood sodium decreased; THROMBOSIS; Blood test; UNRESPONSIVE TO STIMULI; Bronchitis; VENTRICULAR DYSSYNCHRONY; COVID-19; ACUTE SINUSITIS; Catheter placement; ANGIOGRAM CEREBRAL ABNORMAL; Central venous catheterisation; ANGIOGRAM PULMONARY ABNORMAL; Chest pain; ANTIBODY TEST POSITIVE; Chromaturia; BIOPSY BONE MARROW; Computerised tomogram head normal; BLOOD PRESSURE INCREASED; Dyspnoea; BLOOD TEST; Feeling cold; COVID-19; Gastrointestinal tube insertion; CATHETER PLACEMENT; General physical health deterioration; CENTRAL VENOUS CATHETERISATION; Haematocrit; CHEST PAIN; Haemodialysis; CHROMATURIA; Haemofiltration; COMPUTERISED TOMOGRAM HEAD NORMAL; Haemoglobin decreased; DYSPNOEA; Haemorrhoids; FEELING COLD; Headache; GASTROINTESTINAL TUBE INSERTION; Hypervolaemia; GENERAL PHYSICAL HEALTH DETERIORATION; Hyponatraemia; HAEMATOCRIT; Hypotension; HAEMODIALYSIS; Intensive care; HAEMOGLOBIN DECREASED; Livedo reticularis; HAEMORRHOIDS; Mechanical ventilation; HEADACHE; Mucosal hypertrophy; HYPERVOLAEMIA; Nasal flaring; HYPONATRAEMIA; Pain; HYPOTENSION; Peripheral ischaemia; INTENSIVE CARE; Plasmapheresis; LIVEDO RETICULARIS; Red blood cell transfusion; MECHANICAL VENTILATION; SARS-CoV-2 test positive; NASAL FLARING; Secretion discharge; PAIN; Superinfection; PLASMAPHERESIS; Use of accessory respiratory muscles; SUPERINFECTION; Vaccine breakthrough infection; USE OF ACCESSORY RESPIRATORY MUSCLES; White blood cell count increased; This spontaneous report received from a health care professional by a Regulatory Authority Vaccine Adverse Event Reporting System (VAERS), (VAERS reference number 2633017) and concerned a 60 year old male of an unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's concurrent conditions included: bipolar disorder, hypertension, and reflux hypothyroidism. The patient previously received first dose of covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 205A21A, expiry: unknown) dose was not reported, 1 total administered on an unspecified date for an unspecified indication. No adverse events were observed following vaccination with first dose of covid-19 vaccine ad26.cov2.s (Dose number in series 1). The patient additionally received booster dose of covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of administration were not reported, batch number: FL3209, Expiry: unknown) dose was not reported, 1 total administered on 14-MAY-2021 for an unspecified indication. Age at time of vaccination 60 years old. Concomitant medications included levothyroxine, metoprolol, quetiapine, salbutamol, and trazodone. On 02-JUL-2022, the patient experienced arteriosclerosis coronary artery, agonal respiration, bronchiolitis, cardio-respiratory arrest, encephalopathy, hypothermia, respiratory arrest, seizure like phenomena, thrombosis, unresponsive to stimuli, urethral haemorrhage, ventricular dyssynchrony, acute sinusitis, agitation, angiogram cerebral abnormal, angiogram pulmonary abnormal, antibody test positive, biopsy bone marrow, blood pressure increased, blood sodium decreased, blood test, bronchitis, covid-19, catheter placement, central venous catheterisation, chest pain, chromaturia, computerised tomogram head normal, dyspnoea, feeling cold, gastrointestinal tube insertion, general physical health deterioration, haematocrit, haemodialysis, haemofiltration, haemoglobin decreased, haemorrhoids, headache, hypervolaemia, hyponatraemia, hypotension, intensive care, livedo reticularis, mechanical ventilation, mucosal hypertrophy, nasal flaring, pain, peripheral ischaemia, plasmapheresis, red blood cell transfusion, SARS-COV-2 test positive, secretion discharge, superinfection, use of accessory respiratory muscles, vaccine breakthrough infection and white blood cell count increased (Dose number in series 2). Patient presented with shortness of breath and discoloration noted. No new medications, otherwise no new changes. He had body aches, headache and chest pain reported. He was sent for CTA (Computed tomography angiography) with result as no evidence of pulmonary embolus and findings were compatible with bronchitis and superimposed bronchiolitis, multi-vessel as coronary artery calcifications. There was no acute intracranial abnormality. There was no evidence for an acute infarct acute hemorrhage, intracranial mass or hydrocephalus and mild mucosal thickening and frothy secretions in the left maxillary sinus, correlate for symptoms of acute sinusitis his records. When patient was in CT (Computed tomography), there was a code blue, however it was more seizure activity and in unresponsiveness, however it was noted that he did have a pulse and breathing spontaneously. On physician arrival, he had continued mottling. His H-H was 5 17. He was hyponatremic per ED (Emergency department) to lab said his blood could not be processed because it may have been too cold and it was hemolyzed. The patient was excepted to the ICU (intensive care unit). On arrival the patient was breathing spontaneously however not able to follow commands or respond hemodynamically stable. He had an elevated blood pressure, however he had diffuse mottling that was progressive very quickly. Patients mother reported that she was concerned for his infections and had recommended plasma exchange. Patients mother was asked for consent for dialysis catheter central line intubation and the plans with plasma pheresis and she agreed dialysis catheter was placed. There was difficulty placing central line but this was eventually placed. After contacting nephrology for plasmapheresis, low sodium levels were reported. Physician reported that this would have to be corrected first because this was decreased with plasma exchange. He was given bolus of hypertonic saline. There was also a delay in the plasma exchange secondary to the hemorrhoids. The dialysis nurse had to calculate the treatment depending on the hematocrit, however the blood draws were all hemolyzed and intact hematocrit was not able to be obtained. However, physician advised to use the hematocrit of 17 that was taken on arrival. Patient became hypotensive and was started on Levophed. Blood was ordered however patient unfortunately had antibodies and this was still pending screening and matching sounds. The blood that was drawn was too hemolyzed and diluted for them to get accurate results. Covid swab was obtained on arrival to the ICU and that was positive. On 03-JUL-2022, patient had on mechanical ventilation and sedation with propofol and fentanyl. He had an area overnight. He was noted to have worsening again of his skin. Mottling his temperature goal was increased. He was given 4 units PRBCs (packed red blood cells) overnight with plans for IVIG (Intravenous immunoglobulins) per hematology, plasma exchange was not able to be performed secondary to not having enough blood volume. he was started on dialysis. He had apparently the last 2 units of available PRBCs which were being given at that time. Laboratory data included: Angiogram cerebral abnormal, Angiogram pulmonary abnormal, Antibody test Positive, Blood pressure increased, Blood sodium decreased, Blood test pending screening, CT angiography NEG PE bronchitis and superimposed bronchiolitis Hemodialysis placement plasmapheresis repeat, and SARS-CoV-2 test positive Positive. On 04-JUL-2022, Laboratory data included: CT scan negative for changes. Treatment medications (dates unspecified) included: fentanyl, and propofol. Patient had ischemic fingers bilateral. On 04-JUL-2022, head CT was performed which was negative for acute changes. On 06-JUL-2022, patient did not tolerate plasma exchange and continued to hemolyze due to cold temps. CRRT (Continuous renal replacement therapy) was probably contributing to inability to warm him up. On 07-JUL-2022, patients count was improved and was discussed with Heme. Patient continued to be sedated and mechanically ventilated. SBT was planned to be attempted. Temperature was finally controlled off CRRT Tmax 102 WBC (white blood cell) was reported as 13. On 08-JUL-2022, no overnight events were reported. Patient had a lot of subglottic secretions and NG tube was in the esophagus. Some coffee grounds were reported and patient was started on PPI bid (two times a day). Small drop was noted in Hg (blood pressure) but continued to hemolyze by labs. 09-JUL-2022, SBT (Spontaneous breathing trial) was failed and patient was still not following commands. Sedation was reduced and using more precede. Bone marrow biopsy results were seen. On 10-JUL-2022, got agitated off sedation (Dose number in series 1). Attempting SBT seemed to be tolerating, however still encephalopathic precluding a safe extubation. Bone marrow was underwhelming as per oncology. Severe volume overload Continued to have a little bleeding and clots in the urethra. Urine was red and no overt hemolysis and relatively stable Hg plus balance Hypothermic and intermittently febrile. 0n 11-JUL-2022, plus 5 2L 24hrs. He was using accessory muscles with breathing on fentanyl. Ischemic hands bilaterally, Tmax:38 3F. CRRT failed due to hemolysis. He received plasmaphoresis x1 which failed due to clotting previously. On 12-JUL-2022, 1 2L 24hrs, he had vent dyssynchrony overnight and required versed fentanyl pushes. He had an agonal breathing pattern when sedation weaned and nasal flaring. On 13-JUL-2022, plus 9, 5L 24hrs, he successfully completed the second plasmapheresis session. On 12-JUL-2022, pending HD (haemodialysis) . At the day of reporting, despite aggressive care, he continued to decline. After discussion with his mother, she understood his prognosis was poor and did not wish for him to go on living in his current condition and she elected to withdraw care and pursue comfort measures. Patient was then transitioned to inpatient hospice and withdrawal of care implemented (Dose number in series 2). The patient ultimately passed away on 13-JUL-2022 at 18:56 (Dose number in series 2). It was unspecified if an autopsy was performed. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient died on 13-JUL-2022 18:56 from arteriosclerosis coronary artery, agonal respiration, bronchiolitis, cardio-respiratory arrest, encephalopathy, hypothermia, respiratory arrest, seizure like phenomena, thrombosis, unresponsive to stimuli, urethral haemorrhage, ventricular dyssynchrony, acute sinusitis, agitation, angiogram cerebral abnormal, angiogram pulmonary abnormal, antibody test positive, biopsy bone marrow, blood pressure increased, blood sodium decreased, blood test, bronchitis, covid-19, catheter placement, central venous catheterisation, chest pain, chromaturia, computerised tomogram head normal, dyspnoea, feeling cold, gastrointestinal tube insertion, general physical health deterioration, haematocrit, haemodialysis, haemofiltration, haemoglobin decreased, haemorrhoids, headache, hypervolaemia, hyponatraemia, hypotension, intensive care, livedo reticularis, mechanical ventilation, mucosal hypertrophy, nasal flaring, pain, peripheral ischaemia, plasmapheresis, red blood cell transfusion, sars-cov-2 test positive, secretion discharge, superinfection, use of accessory respiratory muscles, vaccine breakthrough infection, and white blood cell count increased. This report was serious (Death, and Hospitalization Caused / Prolonged). This report was associated with a product quality complaint: 90000284580. Additional information was received from central complaint vigilance department on 02-JUN-2023. The following information was updated and incorporated into case narrative: batch number updated for primary vaccine (dose number in series 1).; Sender's Comments: V1: This follow up version updates batch number for primary vaccine (dose number in series 1). This updated information does not alter the causality of previously reported events. 20230567413-death, arteriosclerosis coronary artery, agonal respiration, bronchiolitis, cardio-respiratory arrest, encephalopathy, hypothermia, respiratory arrest, seizure like phenomena, thrombosis, unresponsive to stimuli, urethral haemorrhage, ventricular dyssynchrony, acute sinusitis, agitation, angiogram cerebral abnormal, angiogram pulmonary abnormal, antibody test positive, biopsy bone marrow, blood pressure increased, blood sodium decreased, blood test, bronchitis, catheter placement, central venous catheterization, chest pain, chromaturia, computerised tomogram head normal, dyspnoea, feeling cold, gastrointestinal tube insertion, general physical health deterioration, haematocrit, haemodialysis, haemofiltration, haemoglobin decreased, haemorrhoids, headache, hypervolaemia, hyponatraemia, hypotension, intensive care, livedo reticularis, mechanical ventilation, mucosal hypertrophy, nasal flaring, pain, peripheral ischaemia, plasmapheresis, red blood cell transfusion, secretion discharge, superinfection, use of accessory respiratory muscles, white blood cell count increased. The event shows an incompatible temporal relationship. Therefore, this event is considered inconsistent with vaccine administration. 20230567413-COVID-19, SARS-CoV-2 test positive, Vaccine breakthrough infection. The event is deemed to be scientifically implausible, i.e., there is scientific evidence against a drug/event relationship; AND there is no known class effect. Therefore, this event is considered inconsistent with vaccine administration.; Reported Cause(s) of Death: ARTERIOSCLEROSIS CORONARY ARTERY; AGONAL RESPIRATION; BRONCHIOLITIS; CARDIO-RESPIRATORY ARREST; ENCEPHALOPATHY; HYPOTHERMIA; RESPIRATORY ARREST; SEIZURE LIKE PHENOMENA; THROMBOSIS; UNRESPONSIVE TO STIMULI; URETHRAL HAEMORRHAGE; VENTRICULAR DYSSYNCHRO
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardio-respiratory arrest
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220702; Test Name: SARS-COV-2 TEST POSITIVE; Test Result: Positive ; Test Date: 20220702; Test Name: ANGIOGRAM CEREBRAL; Result Unstructured Data: abnormal; Test Date: 20220702; Test Name: ANGIOGRAM PULMONARY; Result Unstructured Data: abnormal; Test Date: 20220702; Test Name: ANTIBODY TEST; Test Result: Positive ; Test Date: 20220702; Test Name: BIOPSY BONE MARROW; Result Unstructured Data: Bone marrow biopsy results were seen; Test Date: 20220702; Test Name: BLOOD PRESSURE; Result Unstructured Data: increased; Test Date: 20220702; Test Name: COMPUTERISED TOMOGRAM HEAD; Result Unstructured Data: Normal; Test Date: 20220702; Test Name: BLOOD SODIUM; Result Unstructured Data: decreased; Test Date: 20220702; Test Name: BLOOD TEST; Result Unstructured Data: pending screening; Test Date: 20220702; Test Name: CT ANGIOGRAPHY; Result Unstructured Data: NEG PE bronchitis and superimposed bronchiolitis Hemodialysis placement plasmapheresis repeat; Test Date: 20220704; Test Name: COMPUTED TOMOGRAPHY; Result Unstructured Data: negative for changes; Test Name: WHITE BLOOD CELL COUNT; Result Unstructured Data: increased
- Aktuelle Erkrankungen
- Bipolar disorder; Hypertension; Hypothyroidism
- Vorgeschichte
- -
- Andere Medikamente
- ALBUTEROL [SALBUTAMOL]; TRAZODONE; QUETIAPINE; METOPROLOL; LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 07.06.2023
- Impfdatum
- 14.05.2021
- Beginn
- 02.07.2022
- Tage bis Beginn
- 414,0
- Dosis
- 1
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute sinusitis
Agitation
Agonal respiration
Angiogram cerebral abnormal
Angiogram pulmonary abnormal
Angiogram
Angiogram cerebral
Angiogram pulmonary
Antibody test
Antibody test positive
Arteriosclerosis coronary artery
Biopsy bone marrow
Blood pressure increased
Blood sodium decreased
Blood pressure measurement
Blood sodium
Blood test
Bronchiolitis
Symptomtext
Death; BLOOD SODIUM DECREASED; Arteriosclerosis coronary artery; HYPOTHERMIA; Agonal respiration; Bronchiolitis; URETHRAL HAEMORRHAGE; Cardio-respiratory arrest; AGITATION; Encephalopathy; BRONCHITIS; Hypothermia; HAEMOFILTRATION; Respiratory arrest; MUCOSAL HYPERTROPHY; Seizure like phenomena; PERIPHERAL ISCHAEMIA; Thrombosis; RED BLOOD CELL TRANSFUSION; Unresponsive to stimuli; SARS-COV-2 TEST POSITIVE; Urethral haemorrhage; SECRETION DISCHARGE; Ventricular dyssynchrony; VACCINE BREAKTHROUGH INFECTION; Acute sinusitis; DEATH; Agitation; ARTERIOSCLEROSIS CORONARY ARTERY; Angiogram cerebral abnormal; BRONCHIOLITIS; Angiogram pulmonary abnormal; CARDIO-RESPIRATORY ARREST; Antibody test positive; ENCEPHALOPATHY; Biopsy bone marrow; RESPIRATORY ARREST; Blood pressure increased; SEIZURE LIKE PHENOMENA; Blood sodium decreased; THROMBOSIS; Blood test; UNRESPONSIVE TO STIMULI; Bronchitis; VENTRICULAR DYSSYNCHRONY; COVID-19; ACUTE SINUSITIS; Catheter placement; ANGIOGRAM CEREBRAL ABNORMAL; Central venous catheterisation; ANGIOGRAM PULMONARY ABNORMAL; Chest pain; ANTIBODY TEST POSITIVE; Chromaturia; BIOPSY BONE MARROW; Computerised tomogram head normal; BLOOD PRESSURE INCREASED; Dyspnoea; BLOOD TEST; Feeling cold; COVID-19; Gastrointestinal tube insertion; CATHETER PLACEMENT; General physical health deterioration; CENTRAL VENOUS CATHETERISATION; Haematocrit; CHEST PAIN; Haemodialysis; CHROMATURIA; Haemofiltration; COMPUTERISED TOMOGRAM HEAD NORMAL; Haemoglobin decreased; DYSPNOEA; Haemorrhoids; FEELING COLD; Headache; GASTROINTESTINAL TUBE INSERTION; Hypervolaemia; GENERAL PHYSICAL HEALTH DETERIORATION; Hyponatraemia; HAEMATOCRIT; Hypotension; HAEMODIALYSIS; Intensive care; HAEMOGLOBIN DECREASED; Livedo reticularis; HAEMORRHOIDS; Mechanical ventilation; HEADACHE; Mucosal hypertrophy; HYPERVOLAEMIA; Nasal flaring; HYPONATRAEMIA; Pain; HYPOTENSION; Peripheral ischaemia; INTENSIVE CARE; Plasmapheresis; LIVEDO RETICULARIS; Red blood cell transfusion; MECHANICAL VENTILATION; SARS-CoV-2 test positive; NASAL FLARING; Secretion discharge; PAIN; Superinfection; PLASMAPHERESIS; Use of accessory respiratory muscles; SUPERINFECTION; Vaccine breakthrough infection; USE OF ACCESSORY RESPIRATORY MUSCLES; White blood cell count increased; This spontaneous report received from a health care professional by a Regulatory Authority Vaccine Adverse Event Reporting System (VAERS), (VAERS reference number 2633017) and concerned a 60 year old male of an unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's concurrent conditions included: bipolar disorder, hypertension, and reflux hypothyroidism. The patient previously received first dose of covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 205A21A, expiry: unknown) dose was not reported, 1 total administered on an unspecified date for an unspecified indication. No adverse events were observed following vaccination with first dose of covid-19 vaccine ad26.cov2.s (Dose number in series 1). The patient additionally received booster dose of covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of administration were not reported, batch number: FL3209, Expiry: unknown) dose was not reported, 1 total administered on 14-MAY-2021 for an unspecified indication. Age at time of vaccination 60 years old. Concomitant medications included levothyroxine, metoprolol, quetiapine, salbutamol, and trazodone. On 02-JUL-2022, the patient experienced arteriosclerosis coronary artery, agonal respiration, bronchiolitis, cardio-respiratory arrest, encephalopathy, hypothermia, respiratory arrest, seizure like phenomena, thrombosis, unresponsive to stimuli, urethral haemorrhage, ventricular dyssynchrony, acute sinusitis, agitation, angiogram cerebral abnormal, angiogram pulmonary abnormal, antibody test positive, biopsy bone marrow, blood pressure increased, blood sodium decreased, blood test, bronchitis, covid-19, catheter placement, central venous catheterisation, chest pain, chromaturia, computerised tomogram head normal, dyspnoea, feeling cold, gastrointestinal tube insertion, general physical health deterioration, haematocrit, haemodialysis, haemofiltration, haemoglobin decreased, haemorrhoids, headache, hypervolaemia, hyponatraemia, hypotension, intensive care, livedo reticularis, mechanical ventilation, mucosal hypertrophy, nasal flaring, pain, peripheral ischaemia, plasmapheresis, red blood cell transfusion, SARS-COV-2 test positive, secretion discharge, superinfection, use of accessory respiratory muscles, vaccine breakthrough infection and white blood cell count increased (Dose number in series 2). Patient presented with shortness of breath and discoloration noted. No new medications, otherwise no new changes. He had body aches, headache and chest pain reported. He was sent for CTA (Computed tomography angiography) with result as no evidence of pulmonary embolus and findings were compatible with bronchitis and superimposed bronchiolitis, multi-vessel as coronary artery calcifications. There was no acute intracranial abnormality. There was no evidence for an acute infarct acute hemorrhage, intracranial mass or hydrocephalus and mild mucosal thickening and frothy secretions in the left maxillary sinus, correlate for symptoms of acute sinusitis his records. When patient was in CT (Computed tomography), there was a code blue, however it was more seizure activity and in unresponsiveness, however it was noted that he did have a pulse and breathing spontaneously. On physician arrival, he had continued mottling. His H-H was 5 17. He was hyponatremic per ED (Emergency department) to lab said his blood could not be processed because it may have been too cold and it was hemolyzed. The patient was excepted to the ICU (intensive care unit). On arrival the patient was breathing spontaneously however not able to follow commands or respond hemodynamically stable. He had an elevated blood pressure, however he had diffuse mottling that was progressive very quickly. Patients mother reported that she was concerned for his infections and had recommended plasma exchange. Patients mother was asked for consent for dialysis catheter central line intubation and the plans with plasma pheresis and she agreed dialysis catheter was placed. There was difficulty placing central line but this was eventually placed. After contacting nephrology for plasmapheresis, low sodium levels were reported. Physician reported that this would have to be corrected first because this was decreased with plasma exchange. He was given bolus of hypertonic saline. There was also a delay in the plasma exchange secondary to the hemorrhoids. The dialysis nurse had to calculate the treatment depending on the hematocrit, however the blood draws were all hemolyzed and intact hematocrit was not able to be obtained. However, physician advised to use the hematocrit of 17 that was taken on arrival. Patient became hypotensive and was started on Levophed. Blood was ordered however patient unfortunately had antibodies and this was still pending screening and matching sounds. The blood that was drawn was too hemolyzed and diluted for them to get accurate results. Covid swab was obtained on arrival to the ICU and that was positive. On 03-JUL-2022, patient had on mechanical ventilation and sedation with propofol and fentanyl. He had an area overnight. He was noted to have worsening again of his skin. Mottling his temperature goal was increased. He was given 4 units PRBCs (packed red blood cells) overnight with plans for IVIG (Intravenous immunoglobulins) per hematology, plasma exchange was not able to be performed secondary to not having enough blood volume. he was started on dialysis. He had apparently the last 2 units of available PRBCs which were being given at that time. Laboratory data included: Angiogram cerebral abnormal, Angiogram pulmonary abnormal, Antibody test Positive, Blood pressure increased, Blood sodium decreased, Blood test pending screening, CT angiography NEG PE bronchitis and superimposed bronchiolitis Hemodialysis placement plasmapheresis repeat, and SARS-CoV-2 test positive Positive. On 04-JUL-2022, Laboratory data included: CT scan negative for changes. Treatment medications (dates unspecified) included: fentanyl, and propofol. Patient had ischemic fingers bilateral. On 04-JUL-2022, head CT was performed which was negative for acute changes. On 06-JUL-2022, patient did not tolerate plasma exchange and continued to hemolyze due to cold temps. CRRT (Continuous renal replacement therapy) was probably contributing to inability to warm him up. On 07-JUL-2022, patients count was improved and was discussed with Heme. Patient continued to be sedated and mechanically ventilated. SBT was planned to be attempted. Temperature was finally controlled off CRRT Tmax 102 WBC (white blood cell) was reported as 13. On 08-JUL-2022, no overnight events were reported. Patient had a lot of subglottic secretions and NG tube was in the esophagus. Some coffee grounds were reported and patient was started on PPI bid (two times a day). Small drop was noted in Hg (blood pressure) but continued to hemolyze by labs. 09-JUL-2022, SBT (Spontaneous breathing trial) was failed and patient was still not following commands. Sedation was reduced and using more precede. Bone marrow biopsy results were seen. On 10-JUL-2022, got agitated off sedation (Dose number in series 1). Attempting SBT seemed to be tolerating, however still encephalopathic precluding a safe extubation. Bone marrow was underwhelming as per oncology. Severe volume overload Continued to have a little bleeding and clots in the urethra. Urine was red and no overt hemolysis and relatively stable Hg plus balance Hypothermic and intermittently febrile. 0n 11-JUL-2022, plus 5 2L 24hrs. He was using accessory muscles with breathing on fentanyl. Ischemic hands bilaterally, Tmax:38 3F. CRRT failed due to hemolysis. He received plasmaphoresis x1 which failed due to clotting previously. On 12-JUL-2022, 1 2L 24hrs, he had vent dyssynchrony overnight and required versed fentanyl pushes. He had an agonal breathing pattern when sedation weaned and nasal flaring. On 13-JUL-2022, plus 9, 5L 24hrs, he successfully completed the second plasmapheresis session. On 12-JUL-2022, pending HD (haemodialysis) . At the day of reporting, despite aggressive care, he continued to decline. After discussion with his mother, she understood his prognosis was poor and did not wish for him to go on living in his current condition and she elected to withdraw care and pursue comfort measures. Patient was then transitioned to inpatient hospice and withdrawal of care implemented (Dose number in series 2). The patient ultimately passed away on 13-JUL-2022 at 18:56 (Dose number in series 2). It was unspecified if an autopsy was performed. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient died on 13-JUL-2022 18:56 from arteriosclerosis coronary artery, agonal respiration, bronchiolitis, cardio-respiratory arrest, encephalopathy, hypothermia, respiratory arrest, seizure like phenomena, thrombosis, unresponsive to stimuli, urethral haemorrhage, ventricular dyssynchrony, acute sinusitis, agitation, angiogram cerebral abnormal, angiogram pulmonary abnormal, antibody test positive, biopsy bone marrow, blood pressure increased, blood sodium decreased, blood test, bronchitis, covid-19, catheter placement, central venous catheterisation, chest pain, chromaturia, computerised tomogram head normal, dyspnoea, feeling cold, gastrointestinal tube insertion, general physical health deterioration, haematocrit, haemodialysis, haemofiltration, haemoglobin decreased, haemorrhoids, headache, hypervolaemia, hyponatraemia, hypotension, intensive care, livedo reticularis, mechanical ventilation, mucosal hypertrophy, nasal flaring, pain, peripheral ischaemia, plasmapheresis, red blood cell transfusion, sars-cov-2 test positive, secretion discharge, superinfection, use of accessory respiratory muscles, vaccine breakthrough infection, and white blood cell count increased. This report was serious (Death, and Hospitalization Caused / Prolonged). This report was associated with a product quality complaint: 90000284580. Additional information was received from central complaint vigilance department on 02-JUN-2023. The following information was updated and incorporated into case narrative: batch number updated for primary vaccine (dose number in series 1).; Sender's Comments: V1: This follow up version updates batch number for primary vaccine (dose number in series 1). This updated information does not alter the causality of previously reported events. 20230567413-death, arteriosclerosis coronary artery, agonal respiration, bronchiolitis, cardio-respiratory arrest, encephalopathy, hypothermia, respiratory arrest, seizure like phenomena, thrombosis, unresponsive to stimuli, urethral haemorrhage, ventricular dyssynchrony, acute sinusitis, agitation, angiogram cerebral abnormal, angiogram pulmonary abnormal, antibody test positive, biopsy bone marrow, blood pressure increased, blood sodium decreased, blood test, bronchitis, catheter placement, central venous catheterization, chest pain, chromaturia, computerised tomogram head normal, dyspnoea, feeling cold, gastrointestinal tube insertion, general physical health deterioration, haematocrit, haemodialysis, haemofiltration, haemoglobin decreased, haemorrhoids, headache, hypervolaemia, hyponatraemia, hypotension, intensive care, livedo reticularis, mechanical ventilation, mucosal hypertrophy, nasal flaring, pain, peripheral ischaemia, plasmapheresis, red blood cell transfusion, secretion discharge, superinfection, use of accessory respiratory muscles, white blood cell count increased. The event shows an incompatible temporal relationship. Therefore, this event is considered inconsistent with vaccine administration. 20230567413-COVID-19, SARS-CoV-2 test positive, Vaccine breakthrough infection. The event is deemed to be scientifically implausible, i.e., there is scientific evidence against a drug/event relationship; AND there is no known class effect. Therefore, this event is considered inconsistent with vaccine administration.; Reported Cause(s) of Death: ARTERIOSCLEROSIS CORONARY ARTERY; AGONAL RESPIRATION; BRONCHIOLITIS; CARDIO-RESPIRATORY ARREST; ENCEPHALOPATHY; HYPOTHERMIA; RESPIRATORY ARREST; SEIZURE LIKE PHENOMENA; THROMBOSIS; UNRESPONSIVE TO STIMULI; URETHRAL HAEMORRHAGE; VENTRICULAR DYSSYNCHRO
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardio-respiratory arrest
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220702; Test Name: SARS-COV-2 TEST POSITIVE; Test Result: Positive ; Test Date: 20220702; Test Name: ANGIOGRAM CEREBRAL; Result Unstructured Data: abnormal; Test Date: 20220702; Test Name: ANGIOGRAM PULMONARY; Result Unstructured Data: abnormal; Test Date: 20220702; Test Name: ANTIBODY TEST; Test Result: Positive ; Test Date: 20220702; Test Name: BIOPSY BONE MARROW; Result Unstructured Data: Bone marrow biopsy results were seen; Test Date: 20220702; Test Name: BLOOD PRESSURE; Result Unstructured Data: increased; Test Date: 20220702; Test Name: COMPUTERISED TOMOGRAM HEAD; Result Unstructured Data: Normal; Test Date: 20220702; Test Name: BLOOD SODIUM; Result Unstructured Data: decreased; Test Date: 20220702; Test Name: BLOOD TEST; Result Unstructured Data: pending screening; Test Date: 20220702; Test Name: CT ANGIOGRAPHY; Result Unstructured Data: NEG PE bronchitis and superimposed bronchiolitis Hemodialysis placement plasmapheresis repeat; Test Date: 20220704; Test Name: COMPUTED TOMOGRAPHY; Result Unstructured Data: negative for changes; Test Name: WHITE BLOOD CELL COUNT; Result Unstructured Data: increased
- Aktuelle Erkrankungen
- Bipolar disorder; Hypertension; Hypothyroidism
- Vorgeschichte
- -
- Andere Medikamente
- ALBUTEROL [SALBUTAMOL]; TRAZODONE; QUETIAPINE; METOPROLOL; LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 22.05.2023
- Impfdatum
- 07.01.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 91,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Respiratory failure
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE HYPERCAPNIC RESPIRATORY FAILURE RESPIRATORY FAILURE, UNSPECIFIED ACUITY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 01.05.2023
- Impfdatum
- 04.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoxia
Pulmonary embolism
Symptomtext
ACUTE PULMONARY EMBOLISM HYPOXEMIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 10.04.2023
- Impfdatum
- 10.02.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 203,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Brain hypoxia
COVID-19
COVID-19 pneumonia
Cardiac arrest
Death
Disseminated intravascular coagulation
Mechanical ventilation
Multiple organ dysfunction syndrome
Pulse absent
SARS-CoV-2 test positive
Symptomtext
pt brought to hospital post cardiac arrest; brain anoxia; multi-organ failure; positive for COVID; COVID pneumonia; DIC; admitted to hospital for supportive care; on ventilator; after discussion with family they transitioned pt to DNR; pt became pulseless and ventilation support was stopped; pt passed away in the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 10.01.2022
- Beginn
- 20.02.2023
- Tage bis Beginn
- 406,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Atrial fibrillation
Blood creatinine increased
Blood culture negative
C-reactive protein increased
COVID-19
Clostridium difficile infection
Computerised tomogram head normal
Condition aggravated
Culture urine positive
Dementia with Lewy bodies
Depressed level of consciousness
Diarrhoea
Drug screen positive
Enterobacter test positive
Glycosylated haemoglobin normal
Hyperglycaemia
Symptomtext
Patient is a 83 y.o. female patient with history of CAD, paroxysmal A-fib on anticoagulation, ischemic cardiomyopathy, diabetes type 2 insulin-dependent, hypertension, dyslipidemia brought in to Hospital with altered mental status and acute respiratory failure. Acute hypoxic respiratory failure, resolved COVID-19 On admission O2 sat 60%, required NRB and later transitioned to BiPAP in the ED but was able to wean down to RA COVID test positive on 2/14. CRP 132.1> 37 Patient completed isolation. Speech evaluated. Recommended ground meats and thin liquids. Enrolled in hospice at discharge. DC home with hospice C. Difficile Placed on oral vancomycin and continued at discharge to complete 10 days course Isolation precautions Diarrhea improved Continues with poor oral intake Metabolic encephalopathy, improved Lewy body dementia Patient was hard to arouse in the ER Likely due to hypoxia and UTI. Urine drug screen positive for opiates but patient not on opiates at nursing home. Responded some to Narcan CT brain-no acute intracranial abnormality. Unable to do MRI brain due to pacemaker Recurrent admissions for altered mental status Consulted neurology-waxing and waning mentation consistent with Lewy body dementia potentially exacerbated by recurrent infections. Continue Aricept and Namenda. Urinary tract infection Urine culture:> 100,000 Enterobacter cloacae Blood cx NGTD Completed antibiotic therapy Paroxysmal A-fib Ischemic cardiomyopathy S/p DCCV on 2/2/2023, now in sinus rhythm Continue metoprolol, amiodarone 200 mg daily Hypertension Blood pressure stable continue Toprol-XL 25 daily Diabetes type 2 insulin-dependent Home Rx; Lispro SSI. Patient was hyperglycemic initially likely due to steroid and was started on Lantus but titrated down to 5 units HS and DC home on same dose. As patient is enrolling in hospice discontinued lispro SSI AC&HS Hemoglobin A1c from 1/29/2023--6.5% AKI on CKD stage III, resolved Baseline creatinine around 1.5. Admit Cr 1.6, trended up to 2.0, trended down to 1.11 Hydrated with IV fluids Held home Aldactone 12.5 mg daily but restarted No further blood draws. Goals of Care CODE STATUS: DNR CCA Patient was not eating or drinking, not participating in therapy. Discussed with daughter about the option of feeding tube/hospice Daughter wants hospice to be consulted. Hospice saw patient. Patient not a candidate for inpatient hospice. DC home with hospice
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 16,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 13.01.2023
- Impfdatum
- 07.01.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 340,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute myocardial infarction
Acute pulmonary oedema
Acute respiratory failure
Agitation
Anaemia
Anticoagulant therapy
Aspiration
Asthenia
Atrial fibrillation
Bacterial test positive
Bladder catheter removal
Bladder catheterisation
Blood creatinine increased
Blood glucose increased
Blood loss anaemia
Blood urine present
COVID-19
Symptomtext
90 y.o. male with a PMH of Afib (on coumadin), HFpEF, CAD, CKD stage 4, non-hodgkin's lymphoma, COPD (2L NC), T2DM, HLD, hypothyroidism, SSS s/p dual chamber pacemaker. Presented 12/13/22 with generalized weakness. Found to be COVID + and in Afib w/ RVR. Hospitalization complicated by aspiration event with respiratory failure requiring ICU care 12/14-12/15 with HHFNC, development of acute delirium 12/15, and pre renal AKI 12/16. Course further complicated by episode of rectal bleeding overnight 12/20. GI consulted, bleeding scan negative. Course also complicated by persistent Afib RVR and intermittent agitation, also hyperglycemia. Discharged home with HHC on 12/23 with plans for close follow up with PCP. Comments/Problems to be Addressed After Discharge - Repeat BMP outpatient for AKI resolution, resume torsemide outpatient as able - repeat CBC within one week for evaluation of anemia - risk benefit discussion regarding Warfarin and Plavix with PCP - adjust insulin and diabetic regimen PRN Discharge Diagnosis and Associated Hospital Course Rectal Bleeding, Resolved Acute Blood Loss Anemia, Resolved - Concern for lower GIB with bright red blood during hospitalization in setting of anticoagulation - required 1unit pRBC overnight 12/20 - bleeding scan negative 12/21 - GI followed. Will hold warfarin and plavix on discharge. Risk benefit discussed with family and patient's PCP. NIDDM2 Hyperglycemia - On home glipizide 5 mg BID. Etiology of hyperglycemia unclear, decadron could be contributing. - A1c 7.3. Hyperglycemic into the 300-400's. - Continue 10U humalog TID with meals and sensitive sliding scale. Will continue to monitor and adjust as needed. Consider addition of basal insulin on 12/23 - Discharged with sliding scale lispro. Plan for close follow up with PCP outpatient. Ok to resume Glipizide on discharge AKI, improving Baseline Cr ~1.8 to 2. Likely pre-renal in setting of decreased PO intake with restraint use. - Foley removed 12/17 and trial voids appropriate to date - S/p LR 100cc/hr for 10 hours 12/21. - Avoid nephrotoxic agents. Renally dosed Gabapentin to 300mg nightly. Encourage PO intake. Repeat BMP Aspiration Event Occurred in ED on admit with acute hypoxia. Improved with HHFNC in ICU. - again with concern of choking on pill 12/21. Repeat CXR improved - Speech followed. Recommended chopped and thick liquid. Plan for speech therapy with HHC. Acute on Chronic Hypercarbic Respiratory Failure, Resolved - Likely secondary to aspiration event, flash pulmonary edema, subsequent pneumonitis during stay in ED. Less likely secondary to COVID-19 infection, acute HF exacerbation. With chronic COPD on home 2 L, known chronic bilateral pleural effusions. - CXR on admission with bilateral R>L pleural effusions, mild pulmonary vascular congestion. - S/p IV lasix with improvement in respiratory status - Required HHFNC in ICU, weaned to home 2L NC. SpO2 goal 88-92%. Concern for UTI, Resolved - 12/15 PM: patient became acutely delirious, workup for delirium including UA and Urine Cx obtained - UA with large blood, large leukocyte esterase, 24 WBC, 34 RBC, rare bacteria - Urine Cx with coagulase negative staph. - S/p 5 day course rocephin completed. Acute Encephalopathy, Improved - Etiology upon initial presentation likely multifactorial including acute respiratory failure. 12/15/22 event of acute agitation likely secondary to underlying cognitive impairment, sundowning event, possible dexamethasone induced. - UA obtained at time concerning for possible UTI with empiric treatment initiated although unable to determine if symptomatic - Decadron held in setting of acute delirium - intermittently required PRN agitation medication throughout hospitalization. Not continued on discharge Afib w/ RVR, improved - Likely exacerbated in setting of COVID infection, respiratory failure. Family reports unable to tolerate rate control with BB in the past. - Started on cardizem gtt in ED, switched to IV Lopressor with subsequent transition to PO cardizem 240 mg daily 12/15/22. - Holding Warfarin due to GI bleed. Cardizem prescribed on discharge. COVID 19 infection - First developed symptoms 12/12, tested positive 12/13 - Patient vaccinated x3 - ID eConsulted, will hold off on Paxlovid, initially started on Decadron 10 day course - Hold Decadron in setting of acute delirium 12/15, supportive care. Isolation discontinued 12/23 Bilateral pleural effusion Malignant pleural effusion - Etiology likely malignant given history of malignant effusions with marginal zone B-ell lymphoma vs heart failure. - Following discussion with patient, family, and PCP did not pursue thoracentesis. Type II NSTEMI - Secondary to ischemic demand in setting of AF with RVR and aspiration event. With known prior CAD history. Without symptoms consistent with ACS to date. - Admission troponin 146 > 136, below prior baseline - Admission EKG with ST segment abnormalities V2, V3, V5, V6. ST segments appear stable from prior baseline EKG, with new RVR on admission EKG. Chronic HFpEF - Patient reported to follow with Dr. - TTE 02/2021 with EF51%; Repeat Echo with EF50%, borderline pulmonary hypertension - Home regimen: Torsemide 40mg daily - Given 80 mg IV lasix in ED, responded well. Started on 40mg Lasix IV q8 12/14 with plan to transition to home torsemide 12/17/22. - Diuretics held in setting of AKI 12/17. Resume as able outpatient COPD without exacerbation - Per hx on 2L NC at home - Low concern for acute exacerbation, continued home regimen Marginal zone B-cell lymphoma (HCC) - Malignant pleural effusion 12/28/20221 consistent with marginal zone lymphoma. Appears rituximab was held during omicron surge. Per family, patient not pursuing treatment, but would consider it pending need for recurrent thoracentesis - Management per above Sick Sinus Syndrome - s/p dual chamber pacemaker CAD - Follows with Dr., history of MI. Multiple PCI's, last cath 2019: mild CAD with well-preserved LV function. PCI to diagonal. CABG multiple years ago. - Last visit with Dr. in 09/2021, plavix was decreased to three times/ week due to bruising. Instructed to follow up in two years. No end date for plavix. - Continued home statin. Holding plavix and warfarin in setting of GIB. Further discussions with family on risks/ benefits of continuing anticoagulation in setting of high stroke and high bleeding risk. HLD - Continued home statin Hypothyroidism - Continued home synthroid GERD - Continued home protonix Insomnia - Continued home remeron
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 10,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 01.10.2022
- Impfdatum
- 01.01.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 46,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiogenic shock
Death
Myocardial infarction
Symptomtext
Death at Hospital 02/23/2022. Cardiogenic shock Myocardial Infarction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Diabetes
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Cephalexin 500 mg capsule LevemIr Flextouch 100 Unit/ML Losartan Potassium 50 MG Tab
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 24.02.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 158,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
COVID-19
SARS-CoV-2 test positive
Symptomtext
COVID-19 02/02/2022 1 of 2 Comirnaty-PFR 30mcg COVID-19 02/24/2022 2 of 2 Comirnaty-PFR t-s 30mcg Patient admitted with COVID infection 8/1/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- COVID positive 8/1/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- history of mitochondrial myopathy admitted on 8/1/2022 for acute hypoxic respiratory failure caused by current Covid infection. She is admitted for supplemental O2
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 05.01.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 79,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
Epistaxis
Haemoptysis
Haemorrhage
SARS-CoV-2 test positive
Vascular pseudoaneurysm
Symptomtext
Patient tested positive with Covid-19 on 3/25/22. Patient had history of head and neck cancer. Brought to hospital per ENT for inpatient hospice services. Patient admitted with epistaxis, hemoptysis, right distal common carotid artery pseudoaneurysm. Patient continued to have more bleeding and was seen by palliative care, hospice and admitted to inpatient hospice service. Patient expired on 5/6/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 03.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Angle closure glaucoma
Balance disorder
Blood test
Cerebrovascular accident
Coordination abnormal
Electrocardiogram
Eye laser surgery
Impaired work ability
Intraocular pressure increased
Laboratory test
Magnetic resonance imaging
Mobility decreased
Orthosis user
Peroneal nerve palsy
Sleep disorder
Ultrasound Doppler
Urine analysis
Symptomtext
2/7/2022 Woke up in the middle of the night and was very off balance and had to use objects to make it to the bathroom. Began losing use and dexterity of left arm. Symptoms worsened and on the 10th my son had to pick from work and take me to an urgent clinic. After failing multiple coordination and strength tests the Doctor believed I was having a stroke and instructed me to go straight to the ER. He asked if I had a driver or if they needed to provide me with an ambulance. I told him that my son was with me to drive. He wrote me a note to give to the front desk of the ER and told me to get there quick. I arrived at the ER and they performed an MRI, EKG, carotid doppler, blood work, and urine. They determined that I was having a stroke and I was admitted to the hospital. Started working with an occupational therapist. Spent 2 days in the hospital and was discharged with 16 weeks of physical and occupational therapy. Also had an appointment with another department for a brace for my left foot, which had developed drop foot. I was unable to work for 3 months. Neurology insisted I go to the eye doctor to check for loss of peripheral vision, the pressures in my eyes was very elevated so I was sent to a glaucoma specialist. The glaucoma specialist diagnosed me with narrow closure glaucoma. On 4/11 had to have laser surgery on my left eye to relieve the pressure and then the same surgery on the right eye on 04/18.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Angle closure glaucoma
- Hospital-Tage
- 2,0
- Labordaten
- MRI EKG Carotid Doppler Blood work Urine Multiple Eye Tests
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- Sulfa Amoxicillin Contrast Dye
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 17.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 17,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anticoagulant therapy
Cerebral infarction
Cerebrovascular accident
Dizziness
Fulguration
Haematuria
Haemorrhage
Haemorrhagic transformation stroke
Magnetic resonance imaging head abnormal
Thrombectomy
Thrombosis
Transurethral prostatectomy
Visual field defect
Symptomtext
Admitted for left PCA CVA after presenting with dizziness and right sided visual field deficits. MRI showed Medial left occipital lobe infarct. He did have a bit of hemorrhagic conversion that precluded the ability to give him anticoagulation for a few days. He was eventually started on Eliquis and developed recurrent gross hematuria. He was taken to the OR for Limited Bipolar transurethral resection of prostate, fulguration of bleeding vessels, clot evacuation. His Eliquis was resumed the next day and he has not had further hematuria. Discharged to home. Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 13,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Acute respiratory failure
Anaemia
Biopsy liver
Blood lactic acid increased
Bronchoscopy abnormal
Chills
Cholecystectomy
Computerised tomogram thorax abnormal
Echocardiogram normal
Endotracheal intubation
Haemoglobin decreased
Headache
Hepatitis
Hepatobiliary scan abnormal
Intensive care
Laboratory test normal
Leukocytosis
Symptomtext
Received vaccine 1/27, developed fevers that night. She continued to have fever, also had chills, headache, body aches. Developed abdominal distension. Presented to ED on 1/31/2022. Found to have fever, tachycardia, tachypnea, leukocytosis, elevated lactate and abnormal LFTs. She was admitted to the ICU, started on antibiotics for presumed sepsis. Initial suspicion of cholecystitis, went for cholecystectomy and no cholecystitis but liver was inflamed, had biopsy. Subsequently, developed acute hypoxic respiratory failure with CT showing new pulmonary infiltrates. Bronchoscopy done and suggestive of diffuse alveolar hemorrhage, bronch studies pending but so far infectious work up negative. She also developed elevated troponin with normal echo. She developed anemia, required transfusion. She is currently intubated and remains in the ICU with ongoing fevers.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 8,0
- Labordaten
- Abnormal HIDA scan 2/2-2/3 CT chest with pulmonary infiltrates 2/5/2022 Troponin 0.57-0.62 2/5/2022 WBC count 19,000 2/8/2022 Hemoglobin 6.9 2/7/2022 TTE normal 2/2/2022 and 2/7/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 09.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Acute left ventricular failure
Acute myocardial infarction
Arterial disorder
Arteriogram coronary abnormal
Atrioventricular block complete
Atrioventricular block second degree
Cardiac failure congestive
Catheterisation cardiac abnormal
Chest pain
Coronary arterial stent insertion
Coronary artery thrombosis
Echocardiogram abnormal
Ejection fraction decreased
Electrocardiogram abnormal
Pulmonary hypertension
Right ventricular ejection fraction decreased
Troponin increased
Symptomtext
15 days after shot developed substernal chest pain and was seen emergently in the ED and was found to have acute st elevation myocardial infarction (STEMI) requiring emergency cardiac catheterization and had RCA stent placed due to 95% thrombotic lesion and was also found to have 50% LAD lesion. He also had 3rd degree heart block as well as 2nd degree heart block. We was found to have acute systolic congestive heart failure with left ventricular ejection fraction of 32% and mildly reduced right ventricular ejection fraction and moderate pulmonary hypertension was noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 2,0
- Labordaten
- EKG (Acute STEMI), hstroponin 136,400, Coronary angiogram: (acute 95% RCA thrombosis) and 50% LAD lesion, Echocardiogram - LVEF 32%
- Aktuelle Erkrankungen
- No illnesses, was healthy at that time.
- Vorgeschichte
- Cardimyopathy, LVH, sleep apnea, carotid artery stenosis, hyperlipidemia, htn, gout, b12 defeciency, vit d defeciency, gerd, renal disease,
- Andere Medikamente
- Allopurinol, B12, Benicar, flavonoids, Bystolic, coq10, lovaza, niacin, nifedipine, pantoprazole, rosuvastatin, terazosin, vit d
- Allergien
- NKMA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Injection site erythema
Injection site swelling
Myocardial infarction
Symptomtext
Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Additional Details: Patient's partner called on 02/04/2022 to explain Mr. received vaccine on 01/28/22 and passed away shortly after on 01/30/22. She informed that patient developed a lot of swelling at injection site after getting vaccine, went to hospital the day after, and died of a heart attack on 01/30/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate
Heart rate increased
Hyperhidrosis
Myocardial infarction
Palpitations
Panic attack
Symptomtext
resembled a panic or heart attack but not as severe; panic attack; Sweating; Increased heart rate; Pounding heart, racing heart; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP) from medical information team. The reporter is the patient. An 18-year-old male patient received bnt162b2 (PFIZER COVID-19 VACCINE), administered in arm left, administration date 10Jan2022 (Lot number: FL3209) at the age of 18 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Dose 1), for COVID-19 Immunization, reaction: "Had no side effects at all"; Covid-19 vaccine (Dose 2), for COVID-19 Immunization, reaction: "Had no side effects at all". The following information was reported: MYOCARDIAL INFARCTION (medically significant) with onset 13Jan2022, outcome "recovering", described as "resembled a panic or heart attack but not as severe"; PANIC ATTACK (non-serious) with onset 13Jan2022, outcome "recovering", described as "panic attack"; HYPERHIDROSIS (non-serious) with onset 13Jan2022, outcome "recovering", described as "Sweating"; HEART RATE INCREASED (non-serious) with onset 13Jan2022, outcome "recovering", described as "Increased heart rate"; PALPITATIONS (non-serious) with onset 13Jan2022, outcome "recovering", described as "Pounding heart, racing heart". The patient underwent the following laboratory tests and procedures: heart rate: (13Jan2022) increased. Clinical course: The university the patient went to said needed it unless he wanted to do mandatory testing. Patient received his third dose of bnt162b2 (clarified with caller that it was a booster dose) on 10Jan2022. Randomly today (13Jan2022) when he was sitting on the couch watching videos, he developed an extreme panicky feeling that overtook him. It almost resembled a panic or heart attack but not as severe. There was no pain but patient had sweating, increased heart rate, pounding heart, racing heart and feeling panicked all together. There was nothing that was scaring patient or that could increase his heart rate and it came of no where. It was more of a panic attack. Denied any chest pain. Denied any hx of prior panic attacks. Patient had the vaccine a couple of days ago. Patient didn't know if symptoms could still be there for this long after. Patient didn't know if this is from the vaccine or not but it started after he received that third dose. The first two doses that patient had before the third dose, he had no side effects at all. This panicking feeling was on and off and it came back. When the panic attack came it was lessened and not as bad as the first time it happened on 13Jan2022. It started 30 minutes after he ate lunch around 13:30 on 13Jan2022. Provided qualifying statement that this was in no way a diagnosis (ie myocarditis). No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220113; Test Name: Heart rate; Result Unstructured Data: Test Result:Increased
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / OT
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Death
Pyrexia
Symptomtext
On the evening of the booster vaccination (approx 8-9 hours post vaccination), the patient developed fever and chills that progressed over the next 24 hours. On the morning of 1/19/22, the patient's family member discovered the patient had passed away during the overnite
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- At this time unaware of of medical tests
- Aktuelle Erkrankungen
- None identified
- Vorgeschichte
- None identified
- Andere Medikamente
- None identified on medical record
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 14.08.2023
- Impfdatum
- 27.02.2021
- Beginn
- 27.02.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arrhythmia
Fatigue
Hypertension
Injection site rash
Injection site swelling
Pain
Pyrexia
Syncope
Vaccine positive rechallenge
Symptomtext
Each vaccine dose and booster I received resulted in tennis ball sized swelling and rash at the injection site (with pictures to document), and intense fatigue, body aches, fever, fainting, high blood pressure, and arrhythmia (irregular heartbeat) for 7-10 days after each dose with necessary bed rest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- As a healthcare worker, I consulted my boss and coworkers who are medical professionals and they expressed concern that I should go to ER if symptoms worsened but they remained the same. Reported adverse reactions at regular doctors appointment which I could only schedule weeks later after each event.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Influenza seasonal shot
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 09.08.2023
- Impfdatum
- 12.01.2022
- Beginn
- 16.01.2023
- Tage bis Beginn
- 369,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Embolic stroke
Symptomtext
ACUTE STROKE DUE TO EMBOLISM OF UNSPECIFIED ARTERY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Embolic stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 29.06.2023
- Impfdatum
- 10.01.2022
- Beginn
- 04.04.2023
- Tage bis Beginn
- 449,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aortic arteriosclerosis
Arterial disorder
Ischaemic stroke
Physical deconditioning
Transient ischaemic attack
Symptomtext
G45. TRANSIENT CEREBRAL ISCHEMIA 4/4/2023 DECONDITIONING I63.89 SUPERIOR CEREBELLAR ARTERY SYNDROME 5/3/2023 DECONDITIONING I63.9 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 4/17/2023 DECONDITIONING G45.9 TRANSIENT CEREBRAL ISCHEMIA 4/4/2023 ATHEROSCLEROSIS OF AORTA I63.89 SUPERIOR CEREBELLAR ARTERY SYNDROME 5/3/2023 ATHEROSCLEROSIS OF AORTA I63.9 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 4/17/2023 ATHEROSCLEROSIS OF AORTA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 29.04.2023
- Impfdatum
- 07.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 25,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Arthralgia
Asthenia
Blood test
COVID-19
Cytokine test
Electric shock sensation
Electromyogram
Magnetic resonance imaging head
Magnetic resonance imaging spinal
Muscle twitching
Myalgia
Pain in extremity
Pain of skin
Palpitations
Skin burning sensation
Spinal X-ray
Spinal pain
Symptomtext
Since mid February through current, I?ve experienced joint pain, muscle pain, muscle twitching, anxiety, extreme pronounced veins through skin , heart palpitations, brain buzzing and electrical shocks. After getting Covid in July 2022 add to this list extreme leg pain, hip pain and weakness, burning skin pain (similar to small fiber neuropathy), tremors and pain all along the spinal cord.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- MRI of thoracic, cervical, lumbar spine and brain. X-rays of hips and lumbar spine. EMG testing on lower extremities. Ultrasound of veins in legs. Extensive detailed bloodwork including 14 panel cytokine test.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Lyme Disease, Hemochromatosis.
- Andere Medikamente
- Tamsulosin, Fish Oil, Multi Vitamin, probiotic.
- Allergien
- Augmentin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 21.01.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 194,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Pain in extremity
Thrombosis
Ultrasound Doppler abnormal
Symptomtext
I had a sore arm for about three days. On 08/03/2022, I began having soreness in my left calf. I thought I had strained it at work and really didn't think about it. I was advised to get it checked out. I went to the emergency room, and I was given a shot of blood thinner as a precaution. The next day, I had an ultrasound and that was when they saw the blood clot. I was given a prescription to treat the blood clot. As of today, I continue to take the medication and I have a follow up appointment to do blood work.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- 06AUG2022 Ultrasound test, positive blood clot
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 18.01.2023
- Impfdatum
- 10.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angiogram pulmonary
Bell's palsy
Biopsy skin abnormal
Chest X-ray
Dizziness
Electrocardiogram
Hypoaesthesia
Laboratory test
Lumbar puncture
Magnetic resonance imaging
Magnetic resonance imaging head
Paralysis
Small fibre neuropathy
Symptomtext
1/16/22 mid morning had left side facial numbness and paralysis came accompanied with dizziness and decreased sensation to left arm and upper leg to Er in the evening and diagnosed with bells palsy treated with antiviral, steroids, and antibiotic follow up with primary. 9/22/22 er visit for decreased numbness and tingling to bilateral upper and lower extremities and facial numbness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- 1/16 emergency visit with lab work completed and ct/cta, chest X-ray , ekg 9/22/22 mri spine and head, admitted for lumbar puncture, ct head, lab work 11/2022 skin punch biopsy completed with results called as positive for small fiber neuropathy
- Aktuelle Erkrankungen
- Ear ache
- Vorgeschichte
- Exercise induced asthma
- Andere Medikamente
- Started oral antibiotic amoxicillin
- Allergien
- Cefdinir, flagyl
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 26.11.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Heart rate irregular
Loss of consciousness
Nasopharyngeal swab
Syncope
Symptomtext
Since then I started feeling irregular heart beats.; I fainted.; I totally lost my consciousness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old male patient received BNT162b2 (BNT162B2), on 30Dec2021 at 11:30 as dose 3 (booster), single (Lot number: FL3209) at the age of 67 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: ER8727, Location of injection: Arm Left), administration date: 25Mar2021, when the patient was 66-year-old, for COVID-19 Immunization, reaction(s): "I also felt dizziness in Jun2021 without any noticeable reasons"; BNT162b2 (Dose Number: 1, Batch/Lot No: EN6205, Location of injection: Arm Left), administration date: 04Mar2021, when the patient was 66-year-old, for COVID-19 Immunization, reaction(s): "I also felt dizziness in Jun2021 without any noticeable reasons". The following information was reported: SYNCOPE (medically significant) with onset 30Dec2021, outcome "unknown", described as "I fainted."; LOSS OF CONSCIOUSNESS (medically significant) with onset 30Dec2021, outcome "unknown", described as "I totally lost my consciousness"; HEART RATE IRREGULAR (non-serious) with onset 31Dec2021, outcome "not recovered", described as "Since then I started feeling irregular heart beats.". The events "i fainted.", "i totally lost my consciousness" and "since then i started feeling irregular heart beats." required emergency room visit. The patient underwent the following laboratory tests and procedures: Nasopharyngeal swab: Negative. Clinical course: In the morning of 30Dec2021 at about 11:30 patient took Pfizer Booster on his left arm. Same day at night when he went to bathroom standing in front of the toilet, he fainted. He totally lost my consciousness suddenly. He did not know it lasted for how long, but he did not feel cold. When he came back to bed he saw clock time was 2:30 AM. The following morning he went to Emergency Room. The doctor said that the faint was probably related to the Pfizer Booster. Since then he started feeling irregular heartbeats. First, these irregular heartbeats came upon him once in a while, but now it comes up every day and every hour. Very often! It greatly affects his life. He also felt dizziness in Jun2021 without any noticeable reasons. He believed this was the start-up of Pfizer vaccine side effects. Adverse event resulted in: Emergency room/department or urgent care. Patient had no COVID prior vaccination. Patient tested COVID post vaccination. COVID test type post vaccination: Nasal Swab. COVID test result: Negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Test Name: Nasal Swab; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 10.11.2022
- Impfdatum
- 31.05.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Dyspnoea exertional
Electrocardiogram
Fatigue
Immunoglobulin therapy
Laboratory test
Myopericarditis
Pericarditis
Troponin increased
Vomiting
Symptomtext
He just reported to basic training on 5/23/22 and was given the vaccines on 5/31/22. Mother is reporting this. As far as she knows is that he started having some chest pain with vomiting and then the vomiting stopped, the chest pain got worse and worse on activity like running and exercise. Right after he got the vaccines then they went into actual training. Then he started having the symptoms and he reported them to the Supervisor who then sent him over to the clinic. Then they did an EKG and other tests and then he was transported by ambulance to the ER. Then he was admitted with pericarditis. After being admitted then he was diagnosed with myo-pericarditis and was there from 6/2/22 to 6/10/22. Mothers understanding is that he was given steroids, IV fluids, some other medicines such as Colchicine, Solumedrol and 5 treatments with the immunoglobulins. Eventually they started treating him with immunoglobulins, and then once they did that his troponin's started going down as they were elevated. Then he was discharged he went back to the base which the cardiologist put him on no strenuous activity for 6 moths. He continues to have the chest pains. They are doing a med-board process at this time but he cannot stay in the employment unless he is cleared by the cardiologist, and they are still having him with symptoms and is not going to clear him to stay. He is due to have a cardiac stress test to determine if he can stay or not. When he was discharged he was taking a steroid and Ibuprofen but that was discontinued within a couple of weeks. He has not been treated with anything else for his symptoms. Mother states that he says that he is very fatigued and depending on what he is doing activity wise he has the chest pains and shortness of breath. He is being treated at the Facility while on location.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myopericarditis
- Hospital-Tage
- 8,0
- Labordaten
- Multiple in the hospital.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Amoxicillin.
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 22.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
SARS-CoV-2 test
Seizure
Skin burning sensation
Skin exfoliation
Vaccination site exfoliation
Symptomtext
On 04Feb, was at work and was rushed to the emergency room having suffered a seizure / I experienced a 2nd seizure on 16Jul; skin peeling at the injection site and on lower part of the arm and several fingers; skin peeling at the injection site and on lower part of the arm and several fingers; Continued to feel extreme burning sensations at these skin peeling sites; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 22Jan2022 at 10:00 as dose 2, single (Lot number: Fl3209) at the age of 50 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "asthma" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing). Concomitant medication(s) included: LISINOPRIL; AMLODIPINE. Past drug history included: Clindomycin, reaction(s): "Known allergies: clindomycin". Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: Unknown. FC3180, Location of injection: Arm Left, Vaccine Administration Time: 11:00 AM), administration date: 28Aug2021, when the patient was 50-year-old, for COVID-19 Immunization. The following information was reported: SKIN BURNING SENSATION (non-serious) with onset 23Jan2022 at 10:00, outcome "recovered with sequelae", described as "Continued to feel extreme burning sensations at these skin peeling sites"; VACCINATION SITE EXFOLIATION (non-serious), SKIN EXFOLIATION (non-serious) all with onset 23Jan2022 at 10:00, outcome "recovered with sequelae" and all described as "skin peeling at the injection site and on lower part of the arm and several fingers"; SEIZURE (medically significant) with onset 04Feb2022, outcome "recovered with sequelae", described as "On 04Feb, was at work and was rushed to the emergency room having suffered a seizure / I experienced a 2nd seizure on 16Jul". The events "on 04feb, was at work and was rushed to the emergency room having suffered a seizure / i experienced a 2nd seizure on 16jul", "skin peeling at the injection site and on lower part of the arm and several fingers" and "continued to feel extreme burning sensations at these skin peeling sites" required emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (21Sep2022) Negative, notes: Nasal Swab. Therapeutic measures were taken as a result of seizure, vaccination site exfoliation, skin exfoliation, skin burning sensation including painkillers and ointment. Clinical course: After taking 2nd dose on 22Jan2022, the patient went to the emergency room the next day (23Jan2022), with skin peeling at the injection site and on lower part of the arm and several fingers. Continued to feel extreme burning sensations at these skin peeling sites. On 04Feb2022, the patient was at work and was rushed to the emergency room having suffered a seizure. First one she ever had. The patient experienced a 2nd seizure on 16Jul2022. The patient has no covid prior to vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220921; Test Name: Nasal Swab; Test Result: Negative ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; Blood pressure high
- Andere Medikamente
- LISINOPRIL; AMLODIPINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 30.08.2022
- Impfdatum
- 08.06.2022
- Beginn
- 08.08.2022
- Tage bis Beginn
- 61,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram
Aphasia
Asthenia
Balance disorder
Blood test
Computerised tomogram
Echocardiogram
Electrocardiogram
Full blood count
Headache
Hypertension
Hypoaesthesia
Ischaemic stroke
Lipids
Liver function test
Magnetic resonance imaging
Metabolic function test
Pain in jaw
Symptomtext
Ischemic stroke, primary symptom was issues with word choosing, most extreme presentation lasted for about an hour after onset. Lasting effects included issues with word choosing which lasted until after 4pm; minor balance issues and weakness that are ongoing; high blood pressure which is ongoing; transient headaches, jaw pain, and back numbness which are ongoing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- 4,0
- Labordaten
- CT on 8/9/2022, MRI on 8/8/2022, MRA on 8/8/2022, ECG on 8/8/2022, 8/9/2022, 8/11/2022, 2D Echo on 8/9/2022, Carotid duplex bilateral on 8/10/2022, Cardiac TEE on 8/11/2022. Covid test on 8/9/2022, Assorted blood work including BMP, CBC, lipid panel, hepatic function panel, etc. on 8/8/2022, 8/9/2022, 8/10/2022, 8/11/2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high cholesterol
- Andere Medikamente
- Rosuvastatin 20 mg, colon health daily probiotic (not taken daily)
- Allergien
- penicillin
- Vorherige Impfungen
- Tiredness and muscle aches after previous COVID 19 vaccinations Pfizer 4/15/21 Moderna? 5/6/21 Pfizer 11/29/21
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Aphasia
Cold sweat
Cyanosis
Hypotonia
Malaise
Pallor
Syncope
Symptomtext
Patient felt ill after leaving clinic. Patient in company of both parents. Patient fainted but was held by parents. Conscious and breathing but unable to talk, limp extremities, pale, cold clammy skin, bluish pale lips. BP: 52/39 HR:36
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- EpiPen given 0.3mg IM L Thigh
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- none
- Allergien
- peanut egg
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 04.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac monitoring abnormal
Heart rate increased
Hypertension
Loss of consciousness
Pain in extremity
Supraventricular tachycardia
Symptomtext
I went to urgent care for severe pain of my arm, the took my blood pressure. A week later I went to see my PCP for the continued pain in my arm, They noted I had high blood pressure and heart rate. A week later, I passed out and I am now on blood pressure medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- They did heart monitor test and discovered I have SBT's , I will be seeing a Cardiologist in June.
- Aktuelle Erkrankungen
- COVID-19
- Vorgeschichte
- No
- Andere Medikamente
- Birth Control
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Cardiac flutter
Chest discomfort
Fatigue
Palpitations
Chest pain
Cyanosis
Dyspnoea
Echocardiogram abnormal
Exercise tolerance decreased
Pericarditis
Symptomtext
chest pain, SOB, inability to exercise, exercise intolerance, Pericarditis by echocardiogram blue extremities
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- See attached.
- Aktuelle Erkrankungen
- anxiety, depression, fatigue.
- Vorgeschichte
- anxiety, depression, fatigue, possible chronic Lyme disease
- Andere Medikamente
- Lorazepam, 05mg occaissionslly. Vitamin D numerous vitamins and supplements from various practitioners.
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Crying
Fatigue
Fear
Loss of consciousness
Pain of skin
Pruritus
Swelling
Urticaria
Vaccination site hypersensitivity
Vaccination site pain
Vaccination site swelling
Vaccination site urticaria
Vaccination site warmth
Symptomtext
Approx 24 hours after my second COVID vaccination, I can only describe it as the skin on my entire body became intensely painfully, to the point where it made me cry until I passed out from exhaustion. This went on for about 24 hours. My arm around the vaccine site was also burning hot and extremely sensitive. On 01/12/2022, four days after the vaccine, I woke up with horrible hives that started around the vaccine site on my left arm, and eventually covered both arms and both legs. The hives were swollen and very itchy. I self- treated with benedryl tablets (oral) and hydrocortisone cream (topical), because I do not have medical insurance or money for a doctor. The hives lasted approximately one week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None bcs as stated above, I don?t have medical insurance or money for a doctor?s visit. I would definitely have gone to a doctor if I had been able to afford it, it was a very scary reaction.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Gluten allergy and egg allergy
- Andere Medikamente
- Aleve
- Allergien
- Gluten, eggs, thimerosal
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 24.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Electric shock sensation
Pain
Pain in extremity
X-ray normal
Symptomtext
It started 3-7 days after the booster. I still have pain. I can still feel where I got the shot. It goes from the top of my shoulder to my elbow in my left arm. It is pretty constant. It feels kind of like an electrical current running through my arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- X-ray - negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- COPD
- Andere Medikamente
- None
- Allergien
- Codeine; Lanoline
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 11.01.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Seizure like phenomena
Symptomtext
Hospitalization within 6 weeks of COVID vaccination for seizure like activity.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure like phenomena
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 04.04.2022
- Impfdatum
- 14.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Arthralgia
Chest pain
Dyspnoea
Electrocardiogram abnormal
Laboratory test normal
Pain
Pain in jaw
Pericarditis
Troponin normal
Symptomtext
Pericarditis, chest pain radiating to jaw and shoulder associated with shortness of breath that was confirmed on EKG as pericarditis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- EKG: Pericarditis, 01/17/2022, no elevated troponins and otherwise normal labs
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Diabetic ketoacidosis
Dyspnoea
Endotracheal intubation
Respiratory distress
Tracheostomy
Symptomtext
Patient fully vaccinated and boosted with Pfizer on 4/20/21, 5/11/21, and 3/1/22. Patient has a history of type 1 diabetes and ESRD. Presented to ED on 3/3/22 with complaints of shortness of breath. Previously hospitalized for over one month in January for acute respiratory distress requiring intubation and trach. Patient was admitted for DKA on 3/4/22 and discharged on 3/12/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory distress
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 05.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram
Bell's palsy
Ear swelling
Facial paralysis
Fatigue
Gingival swelling
Herpes zoster
Interchange of vaccine products
Magnetic resonance imaging head abnormal
Oedema peripheral
Scan with contrast
Symptomtext
On 1/07/2022-1/09/2022 I had significant swelling in my left armpit and fatigue. The fatigue remained for two weeks. Then on 1/20/2022, I had swelling in my gums, which progressed to my ear. I went to the dentist and then primary care on 1/25/2022 when I was diagnosed with shingles on the mandibular branch of the trigeminal nerve. On 2/10/2022 I had to go the Emergency room as my right facial muscles were paralyzed. I received a Bells Palsy diagnosis secondary to my shingles then. On 3/3/2022 I had an MRI which confirmed the Bells Palsy is still present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- 3/03/2022 MRI of Brain with and without contrast, MRA or Brain and neck. Confirmed Bells Palsy
- Aktuelle Erkrankungen
- Head cold, tested negative for Covid-19 on 12/22/2021
- Vorgeschichte
- Scoliosis and migraines
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Severe migraine with second dose of Modera Covid vaccine on 4/18/2022, two days after the second injection on 4/16/2022
- Staat
- OH
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Blood test
Computerised tomogram normal
Electrocardiogram normal
Facial paralysis
Magnetic resonance imaging normal
Urticaria
Symptomtext
Pt. states that after receiving the 3rd dose of Booster Phizer 12/29/2021 (Influenza Quad x 1), started experiencing symptoms 12/30/2021 of facial hives and facial drooping. 12/31/2021 Emergency Room visit Hospital, EKG, Cat-Scan, MRi preformed to determine no stroke had occurred. Diagnosed with Bells Palsy 01/01/2022. PT with Follow-Up care continue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- Blood Panel 12/31/2021 EKG 12/31/2021 Cat-Scan 12/31/2021 MRI 12/31/2021
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- 2nd dose of Phizer 05/03/2021 (Flu-like symptoms lasting 48hrs)
- Staat
- MO
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Blood test abnormal
Dizziness
Electric shock sensation
Gait disturbance
Hypoaesthesia
Pain in extremity
Peripheral swelling
Sitting disability
Thrombosis
Ultrasound scan
Symptomtext
Dr. did suspect a blood clot; experienced an electrical type sensation of movement that went from my right arm, across my chest, and down to the bottom of my toes; foot pad is swollen; elevated levels of blood test; bottom of foot is painful to walk; bottom of foot is painful to walk; I get light headed; Sitting is equally difficult; my legs fall asleep; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 22Jan2022 09:00 (Lot number: FL3209) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: FLU, administration date 14Jan2022; TETANUS VACCINE, administration date 14Jan2022. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: FA7485), administration date: 17Jul2021, when the patient was 52 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0202), administration date: 18Jun2021, when the patient was 52 years old, for COVID-19 immunization. The following information was reported: THROMBOSIS (medically significant) with onset 22Jan2022 09:45, outcome "not recovered", described as "Dr. did suspect a blood clot"; ELECTRIC SHOCK SENSATION (non-serious) with onset 22Jan2022 09:45, outcome "not recovered", described as "experienced an electrical type sensation of movement that went from my right arm, across my chest, and down to the bottom of my toes"; PERIPHERAL SWELLING (non-serious) with onset 22Jan2022 09:45, outcome "not recovered", described as "foot pad is swollen"; BLOOD TEST ABNORMAL (non-serious) with onset 22Jan2022 09:45, outcome "not recovered", described as "elevated levels of blood test"; PAIN IN EXTREMITY (non-serious), GAIT DISTURBANCE (non-serious) all with onset 22Jan2022 09:45, outcome "not recovered" and all described as "bottom of foot is painful to walk"; DIZZINESS (non-serious) with onset 22Jan2022 09:45, outcome "not recovered", described as "I get light headed"; SITTING DISABILITY (non-serious) with onset 22Jan2022 09:45, outcome "not recovered", described as "Sitting is equally difficult"; HYPOAESTHESIA (non-serious) with onset 22Jan2022 09:45, outcome "not recovered", described as "my legs fall asleep". The events "dr. did suspect a blood clot", "experienced an electrical type sensation of movement that went from my right arm, across my chest, and down to the bottom of my toes", "foot pad is swollen", "elevated levels of blood test", "bottom of foot is painful to walk", "bottom of foot is painful to walk", "i get light headed", "sitting is equally difficult" and "my legs fall asleep" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood test: blood clot; ultrasound scan: unknown results. Therapeutic measures were taken as a result of thrombosis, electric shock sensation, peripheral swelling, blood test abnormal, pain in extremity, gait disturbance, dizziness, sitting disability, hypoaesthesia. Clinical course: No COVID prior to vaccination. No COVID tested post vaccination. No known allergies. Other medications in two weeks: Penicillin. Patient had Ultrasound on legs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- Test Name: blood test; Result Unstructured Data: Test Result:Blood clot; Test Name: Ultrasound on legs; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 16.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaphylactic reaction
Bedridden
Feeling abnormal
Headache
Immunisation
Loss of therapeutic response
Myalgia
Pain
Pyrexia
Vaccination site pain
Symptomtext
Lack of significant antibody response with prior 2 vaccines and booster; second booster; She is having a more robust reaction to her Covid booster, than her prior 3 shots; a little bit of a low grade fever; muscle aches; pain at the injection site; Body aches; headache; staying in bed; felt bad; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. The reporter is the patient. A 53-year-old female patient received bnt162b2 (BNT162B2), administration date 16Jan2022 (Lot number: FL3209) at the age of 53 years as dose 4 (booster), single for covid-19 immunisation. Relevant medical history included: "Immunocompromised" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Methotrexate, notes: She is immunocompromised and has been on Methotrexate, Prednisone, and other medications in the last 6 months; Prednisone, notes: She is immunocompromised and has been on Methotrexate, Prednisone, and other medications in the last 6 months. Vaccination history included: Bnt162b2 (Dose: 01), administration date: May2021, for Covid-19 immunization, reaction(s): "Headache", "sore arm"; Bnt162b2 (Dose: 02), for Covid-19 immunization, reaction(s): "Body aches"; Bnt162b2 (Dose: 03), for Covid-19 immunization, reaction(s): "she is having a more robust reaction to her Covid booster, than her prior 3 shots", "Lack of significant antibody response with prior 2 vaccines and booster". The following information was reported: IMMUNISATION (medically significant) with onset 16Jan2022, outcome "unknown", described as "second booster"; ANAPHYLACTIC REACTION (medically significant) with onset Jan2022, outcome "unknown", described as "She is having a more robust reaction to her Covid booster, than her prior 3 shots"; PYREXIA (non-serious) with onset Jan2022, outcome "recovered" (Jan2022), described as "a little bit of a low grade fever"; MYALGIA (non-serious) with onset Jan2022, outcome "unknown", described as "muscle aches"; VACCINATION SITE PAIN (non-serious) with onset Jan2022, outcome "recovered" (Jan2022), described as "pain at the injection site"; PAIN (non-serious) with onset Jan2022, outcome "recovered" (Jan2022), described as "Body aches"; LOSS OF THERAPEUTIC RESPONSE (non-serious), outcome "recovered", described as "Lack of significant antibody response with prior 2 vaccines and booster"; HEADACHE (non-serious) with onset Jan2022, outcome "recovered" (Jan2022), described as "headache"; BEDRIDDEN (non-serious) with onset Jan2022, outcome "recovered" (Jan2022), described as "staying in bed"; FEELING ABNORMAL (non-serious) with onset Jan2022, outcome "recovered" (Jan2022), described as "felt bad". Clinical course: The caller mentioned that she has an autoimmune disorder and is on a lot of medication. The caller said she has taken 4 Pfizer shots because of her immune deficiency. The caller said she has some good things to say since taking the shot and wants to tell Pfizer so it can help other people. Caller states that she is immunocompromised and has been on Methotrexate, Prednisone, and other medications in the last 6 months. States that on 16Jan2022 she finally managed to get a second dose of the Pfizer Covid booster shot. States that she had normal side effects, nothing else, and that is important so other people like her can have access to another booster. States that people like herself have immune systems that don't product antibodies at the same rate as everyone else. Caller states that after the second booster dose she had a little bit of a low grade fever, muscle aches, and pain at the injection site the next day. States she had no swelling at the site, and the pain went away. Caller says the muscle aches persisted a little bit longer. The second and third day she had a bit of a low grade fever. States that this tells her that her body had a more robust response to the vaccine than any of the previous vaccines. Caller verifies that this was her fourth dose of the Pfizer Covid Vaccine. Caller states that her reaction tells her that her body was producing antibodies. Caller states that she is an attorney. Caller says that she was not supposed to get the fourth shot yet, but her neurologist and internist insisted that it was necessary. Caller states that where she lives no one wears a mask. States she has taken more crap from people for actually putting on a mask. Caller states that she has a stack of questionnaires from Pfizer; none of the questions on them are pertinent. States they seem to be for people who had something worse that what she had, body aches and low grade fever. Caller states she was jubilant that she felt like crap because that means the vaccine was working. Caller states this is something that Research and Development need to know. States that high risk groups, such as herself who hit the genetic jackpot; may take a four shot regimen to adequately produce the antibodies needed to protect people who have autoimmune disorders. Caller says that she doesn't fall into the normal category, so the questions on the forms don't apply to her. Says that they don't get to the heart of the matter. Says Research and Development needs to know that they are going to have to give a higher dose booster or another booster. Caller states that giving someone like her the 2 shots and then a higher octane booster makes sense to her. Caller states for example if you got two shots at 100 then got another at 50; if you bumped that up to 75 and do two of them 5-6 months apart, you could have someone who is protected. Caller states that even with 2 doctors saying she needed the fourth shot she spent so many hours on the phone trying to get it arranged. Caller states that not everyone is the same. Caller says her immune system is wired differently and there are millions of people just like her. Caller says they had a conference of doctors at her local hospital concerning administration of the vaccines and she wasn't even allowed to send a representative. States she didn't even know when it was occurring. Caller states she had to fight it at the front end and now is having to fight it at the back end with this variant. Caller says that her first booster dose of the vaccine was in May2021. Her second booster dose of the vaccine was 16Jan2022. Caller says that she got her first booster as soon as it was available. Caller states that the CDC didn't think ahead. Says they didn't think about people who had it when it was first available and then 6 months down the line. Caller states they are administering fourth shots to hospital personnel. States she found that out through being persistent in calling the hospital systems. Caller says that she got her first booster the same time as hospital personnel; so why wasn't she included in the category for the second booster when they were. Caller states that leaves millions of people, mostly women who are 8 to 1 more likely to have an autoimmune disorder than men; unprotected. Caller says that sounds like a class action law suit. Caller says that a lot of people out there are probably going through their winter flares and they don't have the energy or tenacity to call and call and call so they can get another Booster. She is happy to discuss how she reacted to the second booster because it needs to go ahead and get emergency use approval from the FDA. Caller says can you imagine if someone is on like, Humira? Says it annihilates your immune system.States people on those drugs don't have a choice, its either let your joints be destroyed and don't take it or take it and have no natural defense during a pandemic to a potentially lethal virus. Caller states that would not be a fun place to be. Caller provides no specific information related to the Humira or any patient's as she used this as a hypothetical example. Caller states that is hospital personnel are being given a fourth dose on the sly because of the viral load they are exposed to; why didn't they include people with autoimmune diseases. Caller states that she is a great case. Says she had more of a robust reaction to this dose of the vaccine than she did with her first booster. Caller also states that she had practically no reaction with the first two doses of the vaccine. Says that with her second dose she might have had a low grade fever and a sore arm for an evening, but then she was fine. Caller states that she thinks the only thing that has saved her during the pandemic is she gardens and has stayed in her backyard gardening for the past years. Says she has not gone anywhere, she cannot remember the last time she was in a grocery store. States that is what she has to do to stay safe. Caller says that she is lucky enough to have a yard. What about people with autoimmune conditions who live in apartments? Caller states that the need to be able to be free. Says they will only be able to be free if they can get another booster. Caller says why not let them have another booster. Says they got it when the booster was first available to hospital workers, back in May, Jun, Jul, Aug. Caller states that was way before the general public was encouraged to get the booster. She doesn't understand why this time around they aren't including the immunocompromised. Caller states the only way she got her second booster was her doctor's sent out notes to the pharmacy saying it was medically necessary, so they finally gave her the vaccine. Caller states they even gave her a second vaccination card. Laughs and says its because they know she will be back. States she is going on three years confinement now. Says her husband has a convertible, when she needs to get out at least they can drive around with the top down until she feels less trapped. Caller says that she can be added to whatever other reports Pfizer has. She is willing to have blood drawn, antibody titers, whatever they need to prove that a fourth dose if effective for people in the same category as her. Caller state that people who are walking around with no masks are monsters and she may go to jail for killing one of them. Says the amount of jeering and bullying she has put up with, like people are in grade school. She cannot count the number of times that she has been publicly jeered by these creepy people because she is wearing a mask. Caller says what have we become as a society. Caller says that when she got her second booster she found out that they had 4 cancellations right before her appointment. States maybe that's why she was able to get it, people aren't showing up and they don't want the vaccines to go to waste. States she thinks Pfizer will learn that a second booster is probably a good thing to do with people who are immunocompromised. States that would be the seed for a trial, then there will be a stampede of immunocompromised patients begging for another booster. States Omicron is not the last variant. 25% of the population is a walking petri dish. Caller states who knows what the next variant is going to look like. States Pfizer needs to revamp the questionnaire. States they need a correlation between the severity of symptoms and the amount of antibodies a person is producing. States they need to ask better questions, to get better answers. Caller states its about quality, not quantity. States all it does is generate a bunch of statistics that are meaningless just because people don't feel 110%. Caller says that all four times, each time she got the shot; she wouldn't say that her muscle aches and sore arm and low fever got worse; but they were there a longer period of time. Caller states that tells her her body was working. States with the last shot she got, when she would wake up she was hungry. States that is excellent because her body was working overtime, working hard producing antibodies. Caller says if Pfizer could cut through the volume and get to some cases they might learn something that is good. Caller is calling about an adverse event, from a Pfizer Covid 19 vaccine trial. Later in report, Caller corrects this statement, as she is not in a vaccine trial. Caller got her 4th shot on 16Jan2022. Caller reports she was hungry, and felt like she wanted to sleep. Caller states she is not reporting any adverse events, other than minor events that are listed. Caller states she is immunocompromised and has 4 autoimmune disorders, and on 16Jan2022, received her fourth Covid shot, and clarifies as second booster shot. Caller states she had arranged with her doctors to get a second booster shot because of the lack of significant response to her prior shots. Caller clarifies she is not in a vaccine trial. Caller states because of the recent spike of Covid cases her doctors wanted her to get a second booster. Caller states she will complete a report if it is used for research and development. Caller states she would like to be transferred to the research and development department to see if they have any information on the vaccine with people that are immunocompromised either genetically or because of medications. Caller clarifies she has had no adverse events. Caller states that aside from a headache, fever, and not wanting to get out of bed, she had no events to report. Caller states that aside from a fever, headache, body aches, and staying in bed, she is feeling fine now. Caller states that it is important for the research and development department to know that for immunocompromised patients, the vaccine is proven to be safe and provokes a more robust reaction with the second booster shot, than the original two vaccines and booster. Caller states that the second booster provides a more robust reaction and better production of antibodies than the original two shots and booster. Caller states she is calling because people in her category get overlooked. Caller states she has called Pfizer research and development before, and was instructed to scan for trials to see if she would fit into one of the catagories, to get a second booster. Caller states her and her two doctors felt she was in imminent peril and wanted her to get a second booster. Caller states she finally got a second booster. Caller states she felt bad for 4 days. Caller clarifies that she does not want to report her event. Caller states as someone who is immunocompromised, and is on a tumor necrotizing factor drug, Methotrexate, and Prednisone for the last 6 months for her autoimmune disorders, she wants Pfizer to know that she is having a more robust reaction to her Covid booster, than her prior 3 shots. Caller does not provide product information for her other drugs. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Immunocompromised
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 09.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Anaphylactic reaction
Dyspnoea
Pruritus
SARS-CoV-2 test
Throat tightness
Hypersensitivity
Injection site urticaria
Rash
Injection site rash
Pharyngeal swelling
Urticaria
Symptomtext
anaphylactic reactions; broke out in hives; having difficulty breathing; itchiness/closing of throat; itchiness/closing of throat; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 13 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 09Jan2022 12:00 (Lot number: FL3209) at the age of 13 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: SERTRALINE. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0177, Location of injection: Left arm, Vaccine Administration Time: 03:00 PM), administration date: 14May2021, when the patient was 12 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 2, Location of injection: Left arm, Vaccine Administration Time: 10:00 AM), administration date: 04Jun2021, when the patient was 12 years old, for Covid-19 Immunization. The following information was reported: ANAPHYLACTIC REACTION (hospitalization, medically significant) with onset 09Jan2022 12:00, outcome "recovered" (Jan2022), described as "anaphylactic reactions"; URTICARIA (hospitalization) with onset 09Jan2022 12:00, outcome "recovered" (Jan2022), described as "broke out in hives"; DYSPNOEA (hospitalization) with onset 09Jan2022 12:00, outcome "recovered" (Jan2022), described as "having difficulty breathing"; THROAT TIGHTNESS (hospitalization), PRURITUS (hospitalization) all with onset 09Jan2022 12:00, outcome "recovered" (Jan2022) and all described as "itchiness/closing of throat". The patient was hospitalized for anaphylactic reaction, urticaria, dyspnoea, throat tightness, pruritus (hospitalization duration: 3 day(s)). The events "anaphylactic reactions", "broke out in hives", "having difficulty breathing", "itchiness/closing of throat" and "itchiness/closing of throat" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (12Jan2022) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of anaphylactic reaction, urticaria, dyspnoea, throat tightness, pruritus with Epinephrine shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- 3,0
- Labordaten
- Test Date: 20220112; Test Name: Bionix; Test Result: Negative ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- SERTRALINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 10.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
C-reactive protein increased
Chest pain
Myocarditis
Troponin increased
Symptomtext
Myocarditis Patient developed chest pain 1 day after vaccination. Presented to hospital on 2/6/22 for chest pain and had elevated troponin. Transferred to our facility from other facility. Initial troponin at our facility was 2.296. Troponin peaked on 2/8/22 at 5.873 and then trended down after getting pulse dose steroids (Methylprednisolone 1000 mg daily x 3 doses). Troponin at discharge was 1.008. Patient discharge with steroid taper and follow-up with cardiology.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 5,0
- Labordaten
- Troponin: 2.296 (2/6/22), 1.907(2/6/22), 2.478 (2/7/22), 2.397 (2/7/22), 4.187 (2/7/22), 5.873 (2/8/22), 4.469 (2/8/22), 3.205 (2/8/22), 1.875 (2/9/22), 1.285 (2/9/22), 1.008 (2/10/22) CRP: 30.7 (2/7/22), 14.2 (2/8/22), 9.5 (2/9/22)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- BMI 29.46
- Andere Medikamente
- Fiber gummy, multivitamin gummy
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Syncope
Symptomtext
Patient fainted in the store after leaving the waiting area near pharmacy. Store called 911 and EMT treated patient. Her vitals were checked and found to be normal and they drove patient home
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown as new patient
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Flushing
Hyperhidrosis
Nausea
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 20.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Magnetic resonance imaging head
Scan with contrast
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- 2,0
- Labordaten
- MRI brain with and without contrast
- Aktuelle Erkrankungen
- bacterial vaginosis
- Vorgeschichte
- ADHD, seizure disorder, 8 months post partum, breast feeding
- Andere Medikamente
- carboxymethylcellulose 0.5 % Opht Dpet cetirizine 10 MG Oral tablet diphenhydrAMINE (BENADRYL) 25 mg Oral capsule famotidine 20 MG Oral tablet metroNIDAZOLE 0.75 % Vagl vaginal gel polyvinyl alcohol (ARTIFICIAL TEARS, POLYVIN ALC,) 1.4 % Op
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood glucose normal
Dizziness
Head injury
Loss of consciousness
Seizure
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Became responsive after fainting-Mild, Systemic: Weakness-Mild, Additional Details: Patient loss consciousness and hit his head on the bottom shelf of the aisle, witnessed by a customer stating, "he fell and seizing." Patient was assessed by the immunizer nurse. Per nurse's assesment, patient denied headache, shortness of breath, chest tightness, and visual changes. Patient was able to answer questions. Blood pressure was checked 128/85 with pulse of 102, O2 sat 94%. Blood sugar 99 mg/dL, taken by EMS. Patient was observed for additional 30 mins.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Presyncope
Syncope
Symptomtext
Patient presents vasovagal episode immediately after administration of the vaccine. The patient was lying down with her legs elevated for 30 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient fainted in the store after vaccination but regained conscious shortly. She decided not to leave with the ambulance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Syncope
Symptomtext
PT. FAINTED APROX 3 MINS AFTER RECEIVING COVID-19 VACCINE, SHE FELT DIZZY AND SAT IN CHAIR, FAINTED FOR ABOUT 3 SECONDS, EMTS CALLED EVAULUATED PT, LEFT UNDER OWN WILLPOWER WITH MOTHER AND SISTER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- MOTHER STATED AFTER THE FACT THAT PT HAS FAINTED IN PAST
- Staat
- AZ
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Condition aggravated
Feeling abnormal
Hypotension
Immediate post-injection reaction
Loss of consciousness
Symptomtext
Immediately after 1st pfizer vaccine patient stated he felt weird, then appeared to lose consciousness and possibly have a seizure. He came to, reported that this had happened in the past when receiving a vaccine. Paramedics were called and patient was taken to hospital with extremely low blood pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- BP was 85/50
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Finasteride 1mg
- Allergien
- none
- Vorherige Impfungen
- patient was unsure of what vaccine or when
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Feeling hot
Loss of consciousness
Memory impairment
Symptomtext
Patient was feeling hot and was cooling himself. He got up to get water and passed out not remembering that he had fell. He was taken to be seated with feet elevated to help increase blood flow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n./a
- Vorgeschichte
- n/a
- Andere Medikamente
- medical marijuana
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 29.01.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Myocarditis
Troponin increased
Symptomtext
Severe chest pain starting 3 days after the vaccine. Elevated troponin requiring admission for post-vaccine myocarditis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 3,0
- Labordaten
- HS Troponin 1,336 pg/mL
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Syncope
Symptomtext
Pt walked to waiting area to wait after vaccination and begin to have syncope event while seated within 5 minutes. Patient came to within a few minutes and was offered water. Patient remained seated for next 10 minutes and left when he felt better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose
Depressed level of consciousness
Dizziness
Syncope
Symptomtext
Pt was in chair in observation area when he started becoming lightheaded. His companion asked for water which was provided along with candy. Pt fainted in chair at which time, pharmacist and Clinic NP attended to him. He was slid from chair to floor. He became somewhat conscious but not fully cognizant. NP called for emergency assistance, paramedics arrived, examined him and left approximately 10 minutes later when pt was feeling better
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Paramedics performed blood glucose test
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- n/a
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 31.01.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Syncope
Symptomtext
Patient received 3rd dose, was sitting in chair next to wife. Patient slumped over, at which point wife called for assistance. Patient was quickly roused and was responsive, but a bit weak for about a minute. Offered to call 911, patient declined. Accepted request for water. Pharmacist sat in chair next to patient and wife for about 5 minutes after event. Patient quickly recovered and was advised to continue to sit for about 30 minutes inside of pharmacy to ensure no further adverse event occurred, and inform pharmacist before they left. Sat for about 20 minutes before leaving. Wife had mentioned previously no adverse reactions to previous vaccines, but issues with passing out in past not related to immunizations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No allergies indicated
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 31.01.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pallor
Seizure
Symptomtext
Patient's sister reports patient started "seizing" in the car after they left pharmacy, so they came back. Approximately 30 minutes after patient received the vaccine, patient looked pale, but was alert and coherently speaking.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- unknown
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Malaise
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Medium, Additional Details: Patient became light headed and fainted. After a few seconds patient became alert but was not feeling well enough to stand or sit. Paramedics were called to evaluate patient. After evaluation, it was determined that patient didn't need medical treatment and pt was able to go home on her own after about 20 minutes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 32,0
- Geschlecht
- U
- Eingang
- 27.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Blood test
Chest X-ray
Chest pain
Inflammation
Myocarditis
Pain in extremity
Thrombosis
Vital signs measurement
Symptomtext
Have a blood clot/blood clots to leg; heart inflammation; joint hurting; chest inflammation/chest inflamed; chest hurting; legs hurting/leg pain; This is a spontaneous report received from a contactable consumer or other non hcp. The reporter is the patient. A 32 year-old patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm left, administration date 04Jan2022 (Lot number: FL3209) at the age of 32 years as DOSE 1, SINGLE for COVID-19 immunisation. Relevant medical history included: "none" (unspecified if ongoing). Concomitant medication included: SPRINTEC taken for contraception, start date: 2014 (ongoing). The following information was reported: THROMBOSIS (medically significant), outcome "unknown", described as "Have a blood clot/blood clots to leg"; MYOCARDITIS (medically significant), outcome "unknown", described as "heart inflammation"; INFLAMMATION (medically significant) with onset 05Jan2022, outcome "not recovered", described as "chest inflammation/chest inflamed"; CHEST PAIN (medically significant) with onset 05Jan2022, outcome "not recovered", described as "chest hurting"; PAIN IN EXTREMITY (medically significant) with onset 05Jan2022, outcome "not recovered", described as "legs hurting/leg pain"; ARTHRALGIA (non-serious), outcome "unknown", described as "joint hurting". The patient stated that had a reaction like had chest inflammation and now leg was hurting. The patient went to the Doctor yesterday who said his/her chest inflamed and now legs were hurting. Dr said patient could have a blood clot and took patient's blood yesterday. They were going to be let patient know today what is the results come back, it is a blood clot or it was just joint hurting. The patient had chest inflammation almost for a week and a half. He/she got the vaccine last Tuesday and the next day chest was hurting, could barely eat, could barely talk or laugh. The chest inflammation never felt before. It's very uncomfortable and that's why actually patient wanted to know how long did it stay in their body because really wanted to be out. Was not taking second dose. Patient never felt like this before. Was a healthy person, so had to go to work and it's kind of uncomfortable because had chest inflammation and it's very uncomfortable. He/she went to the emergency room and they were saying patient got the inflammation. The patient saw Doctor yesterday and was told that chest was inflamed and did some blood work and doctor said was going to let patient know today if have a blood clot or if have to go to Emergency or Doctor, if it gets worse really chest inflammation though (Doctor) provide him/her some steroids medicine (Prednisolone), inflammatory medicine yesterday to help with chest inflammation. Doctor said if they don't improve then patient may have to go to the cardiologist over there. The patient also stated that on 06Jan2021 went to the urgent care first they told him/her could have heart inflammation, he/she went to the emergency room to make sure everything is ok, went straight to the emergency room and they took vital sign, took some blood to check for any clots or anything, they give a "chest X-Ray" and patient had to wait for 15 hours, had never seen a Doctor, had never really got result back until to call them the next day but the patient still have a chest pain the next week, that's a new week now. Patient's Doctor yesterday told chest could be inflamed and patient told her legs was hurting, it was hurting, it's kind a hurt a lot and the doctor told the patient to check blood to make sure don't have any blood clots to leg and then gave the patient some steroids or inflammatory medicine, chest improved. Patient's chest was very uncomfortable. The reason for seeing his/her doctor is leg pain, patient was just trying to lay around to top legs up. The events "have a blood clot/blood clots to leg", "heart inflammation", "chest inflammation/chest inflamed", "chest hurting", "legs hurting/leg pain" and "joint hurting" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood work: unknown results; chest x-ray: unknown results; vital sign: unknown results. Therapeutic measures were taken as a result of inflammation, chest pain, pain in extremity. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Test Name: blood work; Result Unstructured Data: Test Result:unknown results; Test Name: chest X-Ray; Result Unstructured Data: Test Result:unknown results; Test Name: vital sign; Result Unstructured Data: Test Result:unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
- Andere Medikamente
- SPRINTEC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose
Loss of consciousness
Symptomtext
Prior to vaccine patient was extremely nervous, after vaccine was administered patient passed out. After about 10 seconds patient came back to and was responsive and aware of his surroundings, he just thought he had a dream.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Blood sugar, pulse, blood pressure and oxygen saturation levels were done
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- THYROID ISSUES
- Andere Medikamente
- levothyroxine
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Fall
Fatigue
Headache
Pyrexia
Syncope
Tinnitus
Vision blurred
Symptomtext
Headache starting at 9:00 AM Syncope event after getting out of bed around (blurred vision, fall, ringing in ears) 1:30 PM Fever 101 noted right after syncope event Fatigue, Weakness throughout day Used damp cloth to cool myself and took Tylenol as directed. Symptoms resolved the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Junel-Fe
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Loss of consciousness
Parosmia
Symptomtext
Pt. states that after receiving the 1st dose of Phizer 01/21/2022, started experiencing symptoms that evening of passing out, "medicine" smell, and fatigue. No noted Primary visit/communications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Bacterium
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Echocardiogram
Pericarditis
Symptomtext
Diagnosed with pericarditis about 10 days after shot was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- Echocardiogram January 19, 2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Metoprolol, Entresto, Xarelto, Vitamin E, Nurtec, Spironolactone
- Allergien
- Sulfa, shellfish
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Chills
Confusional state
Dizziness
Flushing
Hyperhidrosis
Hyperventilation
Syncope
Unresponsive to stimuli
Visual impairment
Symptomtext
Systemic: Chills-Severe, Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Hyperventilation-Medium, Systemic: Visual Changes/Disturbances-Severe, Additional Details: Patient felt weak, fainted once, slumped over in his chair forward, woke back up, was complaining of not being able to see, could only see maybe 2% of visual field, per patient. Paramedics showed up, he fainted again. Pulse of 47, and O2 sats of 95. Paramedics were leaning towards panic attack, but recommended patient go to ER just to be sure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 22.01.2022
- Impfdatum
- -
- Beginn
- 07.01.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anaphylactic reaction
Dizziness
Dysphagia
Dyspnoea
Pharyngeal swelling
Swollen tongue
Throat tightness
Symptomtext
had an anaphylactic reaction to the Pfizer shot and very short of breath; very short of breath; tongue is swollen; throat is swollen shut like patient can barely swallow; throat is swollen shut like patient can barely swallow; patient can barely swallow; Dizzy; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2) (Lot number: FL3209) as dose number unknown, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: ANAPHYLACTIC REACTION (hospitalization, medically significant) with onset 07Jan2022, outcome "not recovered", described as "had an anaphylactic reaction to the Pfizer shot and very short of breath"; DYSPNOEA (hospitalization, medically significant) with onset 07Jan2022, outcome "not recovered", described as "very short of breath"; SWOLLEN TONGUE (hospitalization, medically significant) with onset 07Jan2022, outcome "not recovered", described as "tongue is swollen"; PHARYNGEAL SWELLING (hospitalization, medically significant), THROAT TIGHTNESS (hospitalization, medically significant) all with onset 07Jan2022, outcome "not recovered" and all described as "throat is swollen shut like patient can barely swallow"; DYSPHAGIA (hospitalization, medically significant) with onset 07Jan2022, outcome "not recovered", described as "patient can barely swallow"; DIZZINESS (hospitalization, medically significant) with onset 07Jan2022, outcome "not recovered", described as "Dizzy". Therapeutic measures were taken as a result of anaphylactic reaction, dyspnoea, swollen tongue, pharyngeal swelling, throat tightness, dysphagia, dizziness. Patient was given diphenhydramine (BENADRYL), triamcinolone (DERMAZONE), Epinephrine and sent to the hospital. Patient was released after 5 hours. Patient was sent home with mild dose of diphenhydramine (BENADRYL) and Albuterol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient got the Pfizer booster along with a flu shot. After getting both shots, she sat down on the observation chair in front of the pharmacy. As soon as she noticed she couldn't, she told her grandpa. A technician was there at the time and immediately called the pharmacist for assistance. The patient was taken back to the consultation room where she leaned on the technician for support and fainted on the chair. Her blood pressure was 88/44 and O2 saturation was 98%. We called 911 paramedics. By the time paramedics came, she was stable. Paramedics confirmed she was fine. The last BP reading was 112/68. She declined to be taken to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Dizziness
Loss of consciousness
Nausea
Pallor
Vision blurred
Symptomtext
Patient turned pale after 5-10 min of receiving the vaccine. He felt dizzy, his vision got blurry for a few seconds. He felt nauseous but did not vomit. His heart was hurting. EMTs arrived approximately 15-20 min after vaccine was given. At that time, patient seemed to lose consciousness but was responsive when spoken to. He was taken to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported by the patient
- Vorgeschichte
- None reported by the patient.
- Andere Medikamente
- None listed by the patient
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Additional Details: After He got a shot, he collapsed while he was looking at his cell phone according to his mom. when I went out he was unresponsive a few minutes later. He was responsive a few minutes later, but, we called 911 to check him. Paramedics came and checked him. He was okay according to paramedics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
C-reactive protein
Chest pain
Echocardiogram
Electrocardiogram abnormal
Full blood count
Metabolic function test
Myocardial necrosis marker increased
Myocarditis
Prohormone brain natriuretic peptide
Red blood cell sedimentation rate
SARS-CoV-2 test
Troponin
Symptomtext
chest pain elevated cardiac enzymes abnormal EKG myocarditis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- CBC - 01/18/2022 CMP - 01/18/2022 Troponin - 01/18/2022 Pro-BNP - 01/18/2022 CRP - 01/18/2022 ESR - 01/18/2022 COVID PCR - 01/18/2022 Echocardiogram - 01/18/2022 EKG - 01/18/2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypertriglyceridemia insulinemia and prediabetic range A1c high cholesterol high BMI elevated liver enzymes
- Andere Medikamente
- none
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Seizure
Symptomtext
patient had a seizure that lasted less than 15 seconds and then ems took her to hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none aware of
- Andere Medikamente
- none aware of
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blindness transient
Dizziness
Nausea
Presyncope
Symptomtext
8-10 hours, started 10 hours after vaccine administration: severe lightheadness and dizziness causing temporary vision loss, almost fainting 8-10 hours, started 10 hours after vaccine administration: severe nausea, no vomiting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- 30 mg vyvanse 10 mg lexapro 10 mg Singulair xyzal
- Allergien
- cefdinir, sunscreen
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Syncope
Symptomtext
After receiving immunization within a minute patient fainted and felt very tired after for about 15 minutes. Patient is currently symptom free.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/a
- Vorherige Impfungen
- unknown date - patient's mom said reaction has happened once before
- Staat
- AZ
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Flushing
Loss of consciousness
Unresponsive to stimuli
Symptomtext
After administration of vaccine, patient was feeling light headed. He was seated upright and began to be unresponsive to my conversation. He then lost consciousness and his face became flush red. Chin was lifted to attempt to open airway, as no chest rise was observed. Pulse was assessed and no signs of pulse. A 0.3mg Epinephrine syringe was administered to the patient and consciousness was regained. Patient was starting to become responsive, but not fully coherent. Emergency response was activated and paramedics came to assess the patient. Patient was wheeled out with paramedics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NKDA
- Vorherige Impfungen
- Patient stated that he has a history of fainting or feeling dizzy with any needles, regardless of it being a vaccination.
- Staat
- MD
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anaphylactic reaction
Dyspnoea
Symptomtext
Pt/mother reported anaphylactic reaction approximately 2 hours post-vaccination. Shortness of breath, went to ER and was treated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- allergies, asthma
- Vorgeschichte
- allergies, asthma
- Andere Medikamente
- none
- Allergien
- other vaccines in the past
- Vorherige Impfungen
- unknown date/vaccine -- was reported on form for Covid vaccine
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Head injury
Loss of consciousness
Syncope
Symptomtext
Client was sitting on the chair and suddenly collapsed hitting his head on ground. client was unconscious for a brief moment. Cleint was able to ambulate with assistance to designated emergency area. No sign of injury. client given snack and water. EMS was called, arrived and did assessment. no evidence of injury. Client was cleared by ems. client family was called and took client home. Client stated he had not eaten since yesterday and no fluids since 8 am. Client also stated he has anxiety with needles.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- BP 137/68 P 69 o2 100% rr 18 BP 153/77 p 68 o2 100% BG 110
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Symptomtext
AFTER PT RECEIVING THE VACCINE, PT FELT DIZZY AND PASSED OUT FOR 2 MINUTES.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Pallor
Seizure
Tremor
Unresponsive to stimuli
Vomiting
Symptomtext
patient became pale, starting seizing ~ 5 min after receiving the covid vaccine. her eyes were open, she was sitting up & shaking when RPh arrived. She was however unresponsive when RPh tried to talk to her. Seizure lasted ~ 2 min. Pt threw up at the end of it & then slowly came back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- Patient mentioned after the incident, she had a hx of "passing out"
- Andere Medikamente
- None reported
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypothyroidism, Hypercholesterolemia
- Andere Medikamente
- Levothyroxine, Atorvastatin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Deep vein thrombosis
Pain
Ultrasound Doppler abnormal
Venous occlusion
Symptomtext
Occlusive deep vein thrombosis in lower left leg. Pain began 12 hours after vaccination. Thrombosis confirmed via imaging. Prescribed 5mg Eliquis 2X/day. Visited Emergency dept 1/11/22 for treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Venous Doppler - lower extremities
- Aktuelle Erkrankungen
- COVID-19 14 days prior to vaccine
- Vorgeschichte
- -
- Andere Medikamente
- Levothyroxine Sodium 75mcg
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Condition aggravated
Fatigue
Gait disturbance
Headache
Hypertension
Loss of consciousness
Seizure
Symptomtext
He experienced a seizure. First he had a headache and then the seizure. The seizure lasted for about 30 seconds. He was very weak, tired, and could barely walk. During the seizure, he was not conscious. He went to the school nurse office. His blood pressure was high and he had a persisting bad headache. His blood pressure was at 140/92 and when the nurse tested again, it was at 120/97. He took Ibuprofen that evening. In the evening when I tested his blood pressure, it was at 144/103 at 8:44pm and later 121/89. He felt very tired this morning, but said he started to feel better. He hasn't had a seizure like this in years.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Epilepsy, ADHD, Sleep apnea, Restless leg syndrome
- Andere Medikamente
- Methylphenidate, Oxcarbazepine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Seizure
Syncope
Symptomtext
syncope, seizure. patient recovered after less than 1 minute. patient was assessed by EMS and declined transport to hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- cephalosporins, penicillins
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Pallor
Seizure
Tongue biting
Symptomtext
Patient lost consciousness as observed by accompanying guardian. Per guardian, patient also had a short seizure and skin color turned pale. Episode lasted less than 1 minute. Pharmacist was alerted but patient already regained consciousness and did not need epinephrine or interventions. Recommended patient lower head in seated position to increase blood flow. Patient also bit tongue during episode. Recommended patient stay for another 15 minutes for observation. Followed up with guardian on Monday 1/10/22 and no further incidents reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Presyncope
Symptomtext
Shortly after injection was given, patient had a vasovagal reaction. Patient was helped to the ground and Dr., our on site doctor was called. Patient was placed supine with legs elevated and monitored by clinical staff. Patient recovered shortly and stated that she had not eaten yet today. Patient was given Gatorade and was able to sit in a wheelchair. Patient was monitored for an additional 30 minutes before being released with accompanying family. Patient left under her own power in stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Patient stated she has seasonal allergies.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaphylactic reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Yaz
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 07.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
Patient passed out within 1 minute after the shot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Syncope
Vomiting
Symptomtext
PATIENT WAS LIGHT HEADED, FAINTED AND NAUSEOUS. PATIENT THREW UP CLEAR LIQUID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- NONE REPORTED
- Andere Medikamente
- N/A
- Allergien
- NONE REPORTED
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Additional Details: patient fainted while sitting on bench
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Presyncope
Symptomtext
VasoVagal reaction, passed out
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- Same VasoVagal reaction to other vaccines
- Staat
- IA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Seizure
Syncope
Tongue biting
Symptomtext
Syncope and seizure, bit tongue with seizure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Symptomtext
Administered 2nd dose of the Pfizer covid-19 vaccine to pt and during the 15 minute waiting period, pt passed out for a brief moment (about a few seconds), but came right back to consciousness. She was sitting down in a chair and alert. She stated she felt dizzy, so advised her to stay seated and to take some deep breaths. Told pt we would check on her again in 10 minutes. Pt stated that she expected she could have a reaction like this, so she brought her dad with her for this second dose. Offered to call 911, but pt declined. She had her own water that was drinking as well. She had a similar experience after the 1st dose, but she didn't lose consciousness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Vienva
- Allergien
- Penicillin VK
- Vorherige Impfungen
- Patient stated that she had a similar reaction after the first dose, but she didn't lose consciousness.
- Staat
- PA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 02.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 02.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 31.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hyperhidrosis
Syncope
Tension
Tremor
Symptomtext
tense, sweaty, shaking and to fainty
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- call 911 and paramedic took her for observation
- Aktuelle Erkrankungen
- no known
- Vorgeschichte
- none
- Andere Medikamente
- nortrel tablets
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 08.08.2023
- Impfdatum
- 08.02.2022
- Beginn
- 22.02.2023
- Tage bis Beginn
- 379,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 24.05.2023
- Impfdatum
- 06.01.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 270,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 27.04.2023
- Impfdatum
- 19.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Chest X-ray normal
Chest discomfort
Chest pain
Electrocardiogram normal
Headache
Laboratory test normal
Muscle spasms
Neuralgia
Pain
Paraesthesia
Testicular pain
Tremor
Symptomtext
25 year old male here. A couple days after the first dose of Pfizer, I experienced this discomfort in my left side of my chest (not near the center of my chest, more right in front of my left armpit). Thought nothing of it. Couple days later it started to feel painful. So, 5 days after the first shot, I finally went to the ER and they did all the tests (blood work, EKG, chest x-ray, etc) and it came back normal. The doctor said I might have a pulled muscle or something and to treat it like a sprained ankle (couple weeks recovery). It's now been over a year since the first shot and I have developed severe side effects from the vaccine including chest pain, testicular pain, muscle spasms, headaches, nerve pain, tingling, and muscles shaking. All symptoms have developed over a year long span since vaccination. It began with left side chest pain then I developed all symptoms as weeks went forward since vaccination. I wake up everyday in pain now and this event has changed my entire life. I previously was healthy before the vaccine. I have been to many doctors who are unsure of what?s causing my symptoms but some think that due to me having Covid right before the injection might be why my body isn?t responding well and the reason for my lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Blood work, EKG, stress test, x ray,
- Aktuelle Erkrankungen
- Had COVID-19 2 weeks before vaccination
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 12.03.2023
- Impfdatum
- 15.01.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 21,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Migraine
Palpitations
Tinnitus
Vertigo
Symptomtext
Onset of vertigo, migraines, tinnitus, and racing heartbeat
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Migraine
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Vertigo, migraine, tinnitus, racing heartbeat. Age 58. Vax date 6/15/2021 and 3/27/2021. Pfizer BioNTech Covid 19.
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 25.01.2022
- Beginn
- 15.02.2023
- Tage bis Beginn
- 386,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Atelectasis
Blood creatinine increased
Blood glucose increased
Blood lactic acid
Blood sodium decreased
Chest X-ray abnormal
Chills
Dyspnoea
Full blood count normal
Headache
Hyponatraemia
Hypophagia
Nausea
Oxygen saturation decreased
Pyrexia
SARS-CoV-2 test positive
Vomiting
Symptomtext
Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 2/15/2023 Discharge Date: 2/17/2023 a 58 y.o. female with past medical history of interstitial lung disease/pulmonary fibrosis from COVID 19 infection back in 2021 currently on 2 L nasal cannula with activity, DM type II, hypertension, hypothyroidism, obstructive sleep apnea, coronary artery disease, recently diagnosed ductal cell carcinoma in situ of left breast. She presented to the emergency department on 2/15/23 with fever, chills, headache and shortness of breath, nausea and vomiting. She was not able to eat or drink anything today, she started feeling more short of breath so she presented to the emergency department for evaluation. In the emergency department she was noted to be afebrile, with T max of 38.7 rectally, patient was saturating well on room air, labs were significant for sodium of 132, serum creatinine of 1.11 and blood glucose level of 335, complete blood count was unremarkable, lactic acid was 1.8. Chest x-ray shows subsegmental atelectasis in the right lower lung without focal infiltrate. Viral PCR came back positive for COVID-19 infection, patient desaturated to 87% with ambulation without oxygen. She received Tylenol and albuterol and 1 L normal saline bolus, fever resolved. She was admitted for observation. She clinically improved, Pox was 99% on RA at rest. Nausea and vomiting resolved, and she tolerated well DM liberal diet. Hyponatremia and AKI resolved, creat. on admission was 1.2, at discharge 1.09. DM II well controlled with current meds. She was discharged home on 2/17/2023 Should follow up with PCP as needed and with her onco/ rad onco as scheduled before. She should stay in respiratory isolation until 2/25/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (HCC) OSA (obstructive sleep apnea) Hypothyroidism Hypertension Osteoarthritis Moderate anxiety Mild episode of recurrent major depressive disorder (HCC) CAD (coronary artery disease) Esophageal reflux Moderate persistent asthma without complication Fibromyalgia Abnormally low high density lipoprotein (HDL) cholesterol with hypertriglyceridemia Neuropathy Dense breasts Wrist drop Overweight (BMI 25.0-29.9) Chronic pain Fatty liver Elevated liver enzymes Lumbar spondylolysis Primary osteoarthritis of right hip Renal cyst, right AKI (acute kidney injury) (HCC) Dilated ventricle Painful orthopaedic hardware (HCC) NASH (nonalcoholic steatohepatitis) Arthritis of carpometacarpal (CMC) joint of both thumbs On supplemental oxygen by nasal cannula Presence of neurostimulator Interstitial lung disease (HCC) Depression, major, recurrent, moderate (HCC) Seasonal allergies COVID-19 long hauler manifesting chronic dyspnea COVID-19 long hauler manifesting chronic fatigue COVID-19 long hauler manifesting chronic concentration deficit Other cirrhosis of liver (HCC) Clubbing of nails COVID-19 long hauler manifesting chronic headache Ductal carcinoma in situ (DCIS) of left breast Preoperative examination COVID-19 Respiratory failure (HCC) Viral gastritis Situational anxiety
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet albuterol 2.5 MG/0.5ML nabulizer solution amitriptyline (ELAVIL) 100 MG tablet aripiprazole (ABILIFY) 20 MG tablet Ascorbic Acid (VITAMIN C PO) budesonide/formoterol (SYMBICORT) 160-4.5 MCG/ACT inhaler
- Allergien
- AspirinRash, Asthma/Shortness of Breath CompazineHallucinations PenicillinsAsthma/Shortness of Breath, Throat swelling Red DyeShortness of Breath, Rash Stadol [Butorphanol Tartrate]Hallucinations AdhesiveOther Ace InhibitorsCough NsaidsRash, GI Upset
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 10.02.2023
- Impfdatum
- 07.02.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 256,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthma
Blepharospasm
COVID-19
Chronic obstructive pulmonary disease
Cough
Dyspnoea
Exposure to SARS-CoV-2
Fatigue
Impaired work ability
Malaise
Pain
SARS-CoV-2 test positive
Symptomtext
I had no complications after receiving the vaccine. I was exposed to COVID-19 on 10/11/2022 at a store with someone coughing in my face. I started feeling symptoms of not feeling well on 10/19/2022. I felt like I was hit by a truck, I felt drained, coughing and could not breath. I went to the emergency room because I just could not breath. I was admitted and tested positive for COVID-19 on 10/21/2022. I was out of work for over a month. I have developed COPD, asthma and blepharospasm since having the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 3,0
- Labordaten
- 21OCT2022 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Diabetic; Essential Tremer; Migraines; Myalgia; Hypertension; High Cholesterol; Degenerative Disk Disease
- Andere Medikamente
- Metformin; Atorvastatin; Levothyroxine; Vitamin C Complex; Primidone; Magnesium; Jardiance; Vitamin D; Aspirin; Ibuprofen; Melatonin; Albuterol
- Allergien
- Benadryl; Naproxen; Penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 05.01.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 136,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthma
COVID-19
Chest X-ray normal
Chest pain
Chills
Condition aggravated
Cough
Fatigue
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Narrative: 57 y/o male with PMH for diabetes, hypothyroidism, hypertension, BPH, hyperlipidemia, and asthma. Pt presented to ED with complaints of fever, cough, chills and fatigue on 5/21/22. Pt admitted to hospital with COVID 19, chest pain and asthma exacerbation. Pt treated w/ remdesivir (05/21-05/23), dexamethasone (05/22, 05/23) and azithromycin (05/21, 05/22). Pt improved and discharged to home on 5/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 05/21/2022- COVID 19 positive 05/21/22- Chest x-ray negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 05.01.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 136,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthma
COVID-19
Chest X-ray normal
Chest pain
Chills
Condition aggravated
Cough
Fatigue
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Narrative: 57 y/o male with PMH for diabetes, hypothyroidism, hypertension, BPH, hyperlipidemia, and asthma. Pt presented to ED with complaints of fever, cough, chills and fatigue on 5/21/22. Pt admitted to hospital with COVID 19, chest pain and asthma exacerbation. Pt treated w/ remdesivir (05/21-05/23), dexamethasone (05/22, 05/23) and azithromycin (05/21, 05/22). Pt improved and discharged to home on 05/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 05/21/2022- COVID 19 positive 05/21/22- Chest x-ray negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 04.11.2022
- Impfdatum
- 04.08.2021
- Beginn
- 08.09.2022
- Tage bis Beginn
- 400,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
COVID-19
Chest pain
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
09/08/22 presents to EC ED for "chest pain, abdominal pain, shortness of breath". PMHx of "CVA, DM, breast ca s/p mastectomy and reconstruction, HTN, COVID, open ankle fracture s/p surgical repair"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 09/08/22 SARS-CoV-2 (COVID-19) by detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 22.08.2022
- Impfdatum
- 12.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 20,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Hemiparesis
Hemiplegia
Migraine
Neurological symptom
Symptomtext
Vaccine triggered or caused stroke-like migraines with hemiparesis/hemiplegia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 09.08.2022
- Impfdatum
- 04.02.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 157,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
COVID-19
Cough
Decreased appetite
Fatigue
Feeling abnormal
Headache
Mobility decreased
Pyrexia
SARS-CoV-2 test positive
Throat clearing
Throat irritation
Vomiting
Wheezing
Symptomtext
I had a scratchy throat on July 11th and then on the 12th I was feeling very bad and took a home test and it came out positive. I called my primary care office after testing positive. However they stated that I needed to be seen by a physician before being able to be given PAXLOVID. We talked about options and once she found out that I was on XARELTO I could not do that and then instead I was given the monoclonal antibodies. I did have a fever, low grade, terrible headache, and fatigue. I had no appetite, and I did start to vomit from Wednesday the 13th of July to the 15th of July. I was kept in bed for the whole day each day. Temperature got up to about 101 and on Friday the 15th I was able to receive the infusion. I am still having some symptoms such as coughing, and constantly trying to clear my throat. I did see my primary care doctor again and they stated that they did hear some wheezing so I did receive a steroid inhaler that doesn't help much. The general fatigue is unfortunately still lingering as well. I did retest myself and they came out negative twice.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test: positive; at home COVID-19 test: negative.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Rheumatoid Arthritis; Polymyalgia rheumatica; A-Fib; Chronic Kidney Disease; Osteoarthritis; Hypertension
- Andere Medikamente
- XARELTO; diltiazem; spironolactone; antihistamine; SINGULAIR; prednisone; acepromazine; thalidomide; vitamin B12; calcium; vitamin D3; albuterol inhaler; sustain eye drops; iron supplements; TYLENOL
- Allergien
- Codeine; VOLTAREN; surgical adhesive; environmental allergies
- Vorherige Impfungen
- Shingles vaccine before Shingrix vaccine; localized rash and swelling afterwards.
- Staat
- CO
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 02.05.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Condition aggravated
Cough
Fatigue
SARS-CoV-2 test positive
Upper respiratory tract congestion
Symptomtext
Experienced upper respiratory congestion, cough, and fatigue so took a PCR home test and it was positive. Went to the urgent care and tested positive for COVID-19 as well. Dr. persuaded me not to take PAXLOVID. On 08/01/2022 tested negative for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Arthritis
- Andere Medikamente
- LIPITOR; SINGULAR; MOBIC; ADVAIR; albuterol.
- Allergien
- N/A
- Vorherige Impfungen
- Anthrax vaccine in 2016, had swelling, fatigue, and pain at the site of injection.
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 29.07.2022
- Impfdatum
- 27.01.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 144,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dizziness
Dyspnoea
Fatigue
Headache
Malaise
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 around 06/20/2022 with symptoms of runny nose, sore throat, headache, fatigue, lightheaded, and shortness of breath. I was given monoclonal antibodies on 06/24/2022. I was ill for 7 to 8 days before my symptoms began to improve. I was later prescribed a steroidal inhaler for lingering shortness of breathe and fatigue that I used for 10 days. I am fully recovered with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid antigen test was positive on 06/24/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Lymphocytic Leukemia
- Andere Medikamente
- Atorvastatin; vitamin B
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 27.07.2022
- Impfdatum
- 23.01.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 184,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exposure during pregnancy
Hypertension
Metabolic function test
Symptomtext
I had no idea I had high blood pressure until I went in for my regular prenatal check up. My blood pressure has been running normal during my whole pregnancy. Yesterday my blood pressure was 142/88. It was high enough that my doctor and I have decided that it would be best not to wait for my due date of August 31, 2022 and opt for a cesarean on August 11, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Metabolic Panel Results not back yet.
- Aktuelle Erkrankungen
- COVID-19
- Vorgeschichte
- No
- Andere Medikamente
- Bupropion; hydroxyzine
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 23.01.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 165,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal discomfort
Abdominal pain
COVID-19
Chills
Cystitis
Dyspnoea
Escherichia infection
Escherichia test positive
Fatigue
Inflammation
Malaise
Muscle spasms
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Urine analysis abnormal
Symptomtext
On 7-4-2022, I started having a sore throat. The following day, I just generally did not feel well and had chest congestion. On 7-6, I ran a low grade temp of 100.1. On 7-7, I started having chills. body aches and fatigue. I took a home Covid 19 test with positive results. I called the doctor and they scheduled me a telehealth visit for 7-8. They wanted me to come in for a Covid test so we drove to the back of the clinic drive thru and they tested me for Covid. On 7-9, the doctors office called and told me the PCR was positive and told me just to stay hydrated and to rest. On 7-10, I noticed slight shortness of breath. On 7-11, I started having symptoms of a bladder infection and the doctors office wanted me to come to the office for a urine test which showed Ecoli infection. They prescribed Nitrofurantoin Mono-MCR. On 7-13, I started having abd discomfort/pain. This continued thru morning of 7-16 so I went to the local ER and the doctor gave me an injection of Toradol for the pain/inflammation and another medication that I am not sure of the name but it was for inflammation as well. He felt like it was Covid fatigue muscle spasms. I am feeling a little better today but I still have lingering chest congestion and fatigue. I am reporting my breakthru case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 7-7-2022 home Covid19 test with positive results 7-8-2022 Covid test at Urgent Care with positive PCR 7-11-2022 Urinalysis - positive for Ecoli 7-14-2022 home Covid19 test with negative results
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Rheumatoid Arthritis
- Andere Medikamente
- Humira Inj; Methyltrexate; Folic Acid; Naproxen
- Allergien
- Benedryl
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 01.04.2021
- Beginn
- 30.06.2022
- Tage bis Beginn
- 455,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Dyspnoea
Nausea
SARS-CoV-2 test positive
Sepsis
Vomiting
Symptomtext
Pt to ED 6/29 with SOB and NV x 3 days. COVID+ 6/30, rx Bebtelovimab infusion, not requiring oxygen. 7/2 Pt denies any pain or sob, pt oriented x4. 7/7 Pt A+Ox4, denies any discomfort, denies pain or sob. 7/10 Patient is ambulating to bathroom, denies any trouble urinating, denies pain, denies chest pain/SOB, no S/S of acute distress noted, A&O X 4. 7/11 Patient is A&O x 4, VSS and no S/S of acute distress noted. 7/13 Patients sepsis bpa fired a 5, not concerned with sepsis at time. 7/14 Patient slept throughout the night. Denies pain. No SOB noted. 7/15 pt A & Ox4, cooperative and pleasant. pt discharged 7/16.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 17,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acute exacerbation of chronic obstructive pulmonary disease (COPD) (CMS/HCC) ...Bees [Bee Venom]Swelling, generalized Iodinated Diagnostic AgentsAnaphylaxis/Shock IodineAnaphylaxis/Shock PenicillinsAnaphylaxis/Shock Shellfish AllergySwelling, lips/throat/tongue, Anaphylaxis Shellfish-derived ProductsAnaphylaxis/Shock
- Andere Medikamente
- albuterol (2.5 MG/3ML) 0.083% INHAL ...albuterol (2.5 MG/3ML) 0.083% INHAL Nebu Soln albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln allopurinol (ZYLOPRIM) 100 MG PO Tab amLODIPine (NORVASC) 10 MG PO Tab as
- Allergien
- Bees [Bee Venom], iodinated diagnostic agents ...Bees [Bee Venom]Swelling, generalized Iodinated Diagnostic AgentsAnaphylaxis/Shock IodineAnaphylaxis/Shock PenicillinsAnaphylaxis/Shock Shellfish AllergySwelling, lips/throat/tongue, Anaphylaxis Shellfish-derived ProductsAnaphylaxis/Shock
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 11.07.2022
- Impfdatum
- 08.07.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Paraesthesia
Symptomtext
Symptoms started 5 minutes after injection, patient began to experience numbness in his left leg around the calf and hamstring area. Further description highlights the feeling sensation of patient's leg falling asleep. Subject requested physical examination 3 days later and upon being seen, muscle motor reflexes were checked with no abnormal indications, nor discoloration or swelling to rule our possible blood clotting. Patient was then told by Provider Care Manager (PCM) to continue monitoring conditions and emphasized if conditions change for the worse to seek medical care at nearest emergency room.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None were taken
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Right Uterer Obstruction, Right Kidney Renal Failure, Hydronephrosis, and Hypertension
- Andere Medikamente
- Lisinopril and Zinc
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 14.01.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 75,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Aphasia
Blood pressure increased
Burning sensation
Coagulation test
Computerised tomogram
Dizziness
Electroencephalogram
Electromyogram
Hemiparesis
Laboratory test
Magnetic resonance imaging
Muscle twitching
Nerve conduction studies
Paraesthesia
Photophobia
Ultrasound Doppler
Symptomtext
Muscle twitching on right side, burning and tingling on right side, tingling to back of head, episodes of being unable to speak, episodes of elevated blood pressure, feeling faint, sensitive to flashing lights and certain patterns in black and white. Started with burning sensation over whole body, weakness on right side, and inability to speak on March 30, 2022 and the above progressed afterwards.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- CT scans, MRI, EEG, carotid ultrasound, Factor V Leiden, EMG and nerve conduction, several labs
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN
- Andere Medikamente
- Labetalol Zoloft
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 25.06.2022
- Impfdatum
- 13.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Confusional state
Feeling abnormal
Gait disturbance
Head discomfort
Computerised tomogram
Dysgraphia
COVID-19
Drug ineffective
SARS-CoV-2 test
Grip strength decreased
Headache
Hypoaesthesia
Laboratory test
Magnetic resonance imaging
Musculoskeletal discomfort
Nausea
Neck pain
Symptomtext
the caller is positive with Covid; the caller is positive with Covid; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 51-year-old female patient received BNT162b2 (BNT162B2), on 24Apr2021 as dose 1, single (Lot number: ER8736), on 31May2021 as dose 2, single (Lot number: EW0173) and on 13Jan2022 as dose 3 (booster), single (Lot number: FL3209) at the age of 51 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "the caller is positive with Covid". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: the caller is positive with Covid. It was reported that, the caller stated that she had her 1st dose of the Pfizer BioNTech Covid 19 vaccine, 2nd dose and a booster and she had severe adverse reaction after the booster. Right now she had neurological problems with tremors on the right side of her body on her arm and hand and states she also had a problem with walking a little bit. Agent (Name withheld) caller also had onset migraine since January and she states that this headache was not go away. She had to be on Tylenol and Ajovi which she took monthly to help the pain. Agent (Name withheld) the caller states she was hearing of more and more problems with neurological disorders after the vaccine. Agent (Name withheld) the caller states that her daughter was positive to Covid and her mother, and the caller was positive with Covid. Agent (Name withheld) the caller asked how long does it take for the vaccine to get out of your body. Agent (Name withheld) that she had 2 dates and she was not sure what they go to, she has 14Jan and 31May but did not know what they were for. States she thinks 31May was the last administration of Ajovi and 14Jan is the day she got the booster. Agent states she will have to listen to the call to get the correct details. Caller states this was from the vaccine, she did not have this before. Caller states she just wanted to know if there was anything to take it out of her body. Agent was heard stating she understand but she did not have that kind of information. Caller states that today was day 10 of having Covid. States that she had the symptoms starting after the 2nd vaccine dose and the 3rd was more severe and had not gone away. States the 2nd vaccine dose, the morning after she had the onset headache and numbness in her arms, legs and feet. Caller states with the 3rd dose she has nausea, severe nausea and onset of pain in her head again with numbness but with tremors on her right side and difficulty walking. States she was not having difficulty walking after her 2nd dose. Caller states she was worried about her health and has been in the ER multiple times and was hospitalized once. Caller states she was going on 5 months with these symptoms. Patient Details: Call states this was a previous weight, she thinks she lost a little weight. Caller states she worked in ER for years and was not working now due to this. Prescribing Healthcare Professional Info: States she has 2 neurologists, she has one from before her condition worsened and sees a new one listed in formal field. Caller does not have email to provide. Caller states she called and reported when she 1st started symptoms in she thinks Feb2022 and called again today as she had been in the ER multiple times and her symptoms worsened to tremors on the right side of her body. Caller does not have Report number to provide. States the tremors on her right hand and her arm are new to report. She believes when 1st reported she just had numbness and now it was difficult to walk, she has weakness and heaviness in her legs. Caller states she was 50 and healthy when she got the vaccines, she ran on the treadmill and did the stair master. Caller states the tremors started she would say probably in the last week. States they are getting worse because it was more severe pain in her head and that was what bring on the tremors. Caller states when she spoke to the agent she said that in the trials they had reports of others with headaches. Caller states the difficulty walking she would say started within the last 3 weeks and feels like it is staying the same. Caller states she went to her pharmacist and they said people are coming in for Ajovi. Caller states her headache was severe, it was bad where it was pressure. Caller states she was hospitalized once for a lumbar puncture on she believes it was on 30Mar2022 and discharged 01Apr2022. Caller clarifies that she was admitted to the hospital on 26Mar2022, they did the lumbar puncture on 27Mar2022 and she was discharged on 28Mar2022. Caller states she went back to the ER and was admitted to observation on 31Mar2022 and they did a blood patch on her and she was discharged on 01Apr2022. Caller would like to add with terrible pain in her head and numbness on her right side she have confusion that had even affected her, like foggy brain and memory, forgetful memory. States that started when she was admitted in the hospital before the lumbar puncture. Caller clarifies that she did have it the 1st time she reported, she felt disoriented and that was in Feb2022 with her 1st ER visit and she had a MRI. Caller states she has had problems with her vision and all of her symptoms started in Feb2022 and have progressively gotten worse. Caller states her question she was having is if we know how long it takes the vaccine to get out of her system, she is going on 5 months of these. Caller was asking if she should call her pharmacist. States the agent said she did not have information. Caller states she hopes they find whatever was causing these headaches with trials and information. Caller states it was really scary and she was a healthy person before and going through this was traumatizing to her. States she registered so many patients at the beginning of Covid and she was like this now and she just wanted to get better. There was a product complaint to report. Description of Product Complaint: Description of complaint: positive for Covid Product strength and count size dispensed: not probed. Additional lot numbers: EW0173, FL3209 was a sample of the product available to be returned, if requested: NA. Packaging sealed and intact: not probed. As part of the lack of effect simplification process, the following complaint records were classified as product use attributes lack of effect and have been moved to closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'one and done' business process according to in PQS Q1215 and/or Q1252. Investigation results and conclusions: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE INJECTABLE lot ER8736 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of complaint history for the reported lot. The final scope was determined to be the reported finished goods lot ER8736, fill lot EP8688, and the formulated drug product lot EP8585. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Investigation results and conclusions: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot FL3209 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot FL3209, fill lot FL5838, and the formulated drug product lot FL3183. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Test Name: the caller is positive with Covid; Test Result: Positive ; Comments: the caller is positive with Covid
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 25.06.2022
- Impfdatum
- 13.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Confusional state
Feeling abnormal
Gait disturbance
Head discomfort
Computerised tomogram
Dysgraphia
COVID-19
Drug ineffective
SARS-CoV-2 test
Grip strength decreased
Headache
Hypoaesthesia
Laboratory test
Magnetic resonance imaging
Musculoskeletal discomfort
Nausea
Neck pain
Symptomtext
the caller is positive with Covid; the caller is positive with Covid; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 51-year-old female patient received BNT162b2 (BNT162B2), on 24Apr2021 as dose 1, single (Lot number: ER8736), on 31May2021 as dose 2, single (Lot number: EW0173) and on 13Jan2022 as dose 3 (booster), single (Lot number: FL3209) at the age of 51 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "the caller is positive with Covid". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: the caller is positive with Covid. It was reported that, the caller stated that she had her 1st dose of the Pfizer BioNTech Covid 19 vaccine, 2nd dose and a booster and she had severe adverse reaction after the booster. Right now she had neurological problems with tremors on the right side of her body on her arm and hand and states she also had a problem with walking a little bit. Agent (Name withheld) caller also had onset migraine since January and she states that this headache was not go away. She had to be on Tylenol and Ajovi which she took monthly to help the pain. Agent (Name withheld) the caller states she was hearing of more and more problems with neurological disorders after the vaccine. Agent (Name withheld) the caller states that her daughter was positive to Covid and her mother, and the caller was positive with Covid. Agent (Name withheld) the caller asked how long does it take for the vaccine to get out of your body. Agent (Name withheld) that she had 2 dates and she was not sure what they go to, she has 14Jan and 31May but did not know what they were for. States she thinks 31May was the last administration of Ajovi and 14Jan is the day she got the booster. Agent states she will have to listen to the call to get the correct details. Caller states this was from the vaccine, she did not have this before. Caller states she just wanted to know if there was anything to take it out of her body. Agent was heard stating she understand but she did not have that kind of information. Caller states that today was day 10 of having Covid. States that she had the symptoms starting after the 2nd vaccine dose and the 3rd was more severe and had not gone away. States the 2nd vaccine dose, the morning after she had the onset headache and numbness in her arms, legs and feet. Caller states with the 3rd dose she has nausea, severe nausea and onset of pain in her head again with numbness but with tremors on her right side and difficulty walking. States she was not having difficulty walking after her 2nd dose. Caller states she was worried about her health and has been in the ER multiple times and was hospitalized once. Caller states she was going on 5 months with these symptoms. Patient Details: Call states this was a previous weight, she thinks she lost a little weight. Caller states she worked in ER for years and was not working now due to this. Prescribing Healthcare Professional Info: States she has 2 neurologists, she has one from before her condition worsened and sees a new one listed in formal field. Caller does not have email to provide. Caller states she called and reported when she 1st started symptoms in she thinks Feb2022 and called again today as she had been in the ER multiple times and her symptoms worsened to tremors on the right side of her body. Caller does not have Report number to provide. States the tremors on her right hand and her arm are new to report. She believes when 1st reported she just had numbness and now it was difficult to walk, she has weakness and heaviness in her legs. Caller states she was 50 and healthy when she got the vaccines, she ran on the treadmill and did the stair master. Caller states the tremors started she would say probably in the last week. States they are getting worse because it was more severe pain in her head and that was what bring on the tremors. Caller states when she spoke to the agent she said that in the trials they had reports of others with headaches. Caller states the difficulty walking she would say started within the last 3 weeks and feels like it is staying the same. Caller states she went to her pharmacist and they said people are coming in for Ajovi. Caller states her headache was severe, it was bad where it was pressure. Caller states she was hospitalized once for a lumbar puncture on she believes it was on 30Mar2022 and discharged 01Apr2022. Caller clarifies that she was admitted to the hospital on 26Mar2022, they did the lumbar puncture on 27Mar2022 and she was discharged on 28Mar2022. Caller states she went back to the ER and was admitted to observation on 31Mar2022 and they did a blood patch on her and she was discharged on 01Apr2022. Caller would like to add with terrible pain in her head and numbness on her right side she have confusion that had even affected her, like foggy brain and memory, forgetful memory. States that started when she was admitted in the hospital before the lumbar puncture. Caller clarifies that she did have it the 1st time she reported, she felt disoriented and that was in Feb2022 with her 1st ER visit and she had a MRI. Caller states she has had problems with her vision and all of her symptoms started in Feb2022 and have progressively gotten worse. Caller states her question she was having is if we know how long it takes the vaccine to get out of her system, she is going on 5 months of these. Caller was asking if she should call her pharmacist. States the agent said she did not have information. Caller states she hopes they find whatever was causing these headaches with trials and information. Caller states it was really scary and she was a healthy person before and going through this was traumatizing to her. States she registered so many patients at the beginning of Covid and she was like this now and she just wanted to get better. There was a product complaint to report. Description of Product Complaint: Description of complaint: positive for Covid Product strength and count size dispensed: not probed. Additional lot numbers: EW0173, FL3209 was a sample of the product available to be returned, if requested: NA. Packaging sealed and intact: not probed. As part of the lack of effect simplification process, the following complaint records were classified as product use attributes lack of effect and have been moved to closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'one and done' business process according to in PQS Q1215 and/or Q1252. Investigation results and conclusions: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE INJECTABLE lot ER8736 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of complaint history for the reported lot. The final scope was determined to be the reported finished goods lot ER8736, fill lot EP8688, and the formulated drug product lot EP8585. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Investigation results and conclusions: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot FL3209 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot FL3209, fill lot FL5838, and the formulated drug product lot FL3183. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Test Name: the caller is positive with Covid; Test Result: Positive ; Comments: the caller is positive with Covid
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 152,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Balance disorder
Condition aggravated
Dizziness
Feeling abnormal
Head titubation
Impaired work ability
Loss of personal independence in daily activities
Nausea
Vertigo
Vestibular neuronitis
Symptomtext
Had not had flare up of vestibular neuritis x10 years; current exacerbation/flare up is secondary to Covid vaccine. Miserable. Horrible vertigo, nausea, balance problems, constant head tremors/bobbing, body swaying while standing, unable to perform daily activities, can?t work (I?m unable perform duties safely as I appear drunk), symptoms lasts for weeks, unable to work yet unable to get assisted leave because I?m part-time. I?ve known that the flu vaccine triggers a flare up for me in the past and since I?ve not taken it for past 10 years, I?ve not had any flare ups. When Covid vaccine was mandated, I tried to get exemption but all my physicians were afraid to do so due to reimbursements. Spoke with in-house infectious disease and he was no help. As I am the only provider in household, I had to have an income so I had no choice but to get the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoporosis, Vestibular neuritis
- Andere Medikamente
- Ca citrate, Hydrochlorothiazide, Vit D3, Pepcid, Zyrtec, Turmeric, Metanx
- Allergien
- Flu vaccine, ETOH, Avelox
- Vorherige Impfungen
- Flu vaccine; causes vestibular neuritis flare up
- Staat
- IL
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 12.01.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 135,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Atrial fibrillation
Atypical pneumonia
COVID-19
Cardiac failure
Cardiomegaly
Chest X-ray abnormal
Condition aggravated
Inappropriate schedule of product administration
Lung consolidation
SARS-CoV-2 test positive
Symptomtext
Patient received pfizer vaccine on 6/7/21, 7/23/21, and 1/12/22. Presented to Hospital on 5/27/22 and found to be COVID positive. She was admitted with a provisional diagnosis of suspected decompensated heart failure secondary to longstanding known HFpEF complicated by paroxysmal atrial fib with a rapid ventricular response. ON room air the whole admission and not placed on any treatment specific to COVID19. Discharged on 5/31/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atypical pneumonia
- Hospital-Tage
- 4,0
- Labordaten
- 5/27/22 COVID19: positive 5/27/22 chest xray: Cardiomegaly worse compared to prior. Pericardial effusion not excluded. Consolidative changes left greater than right lower lung zones as seen with atypical pneumonia such as COVID-19.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- severe degenerative arthritis of the knees with contractures combined with her advanced age and general weakness, which has left her in a bed and chair-ridden state. She has severe sarcopenia. She has longstanding type 2 diabetes, the previously noted heart failure with preserved ejection fraction, chronic persistent atrial fibrillation with an elevated CHADS-VASc score as well as elevated HASBLED score, which has prompted us to pursue anticoagulant therapy, albeit in lower doses. Additionally, she has developed an acute DVT in her lower extremities about 6 months ago. She has chronic renal insufficiency, dyslipidemia, hypothyroidism, diverticular disease, chronic low back pain, history of Reglan-induced tardive dyskinesia with choreoathetoid movements in the oral area, which is stable and not progressed.
- Andere Medikamente
- 1. Tylenol 650 q.4 h. p.r.n. 2. Apixaban 2.5 b.i.d. 3. Gabapentin 100 mg at night. 4. Metoprolol 25 mg daily. 5. Bumetanide 2 mg daily. 6. Metolazone 5 mg daily. 7. Potassium 20 mEq daily. 8. Donepezil 5 mg nightly. 9. Levothyrox
- Allergien
- Quinapril, pioglitazone, lyrica, lisinopril
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Chest pain
Electrocardiogram
Insomnia
Laboratory test
Magnetic resonance imaging
Periarthritis
X-ray limb
Symptomtext
The same day as vaccine second booster acerbated pain in shoulder. Next day went ER diagnosed with Frozen shoulder, medicine prescribed were methocarbamol, naproxen, Voltaren. EKG done at ER due to chest pain. Difficulty sleeping due to pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Labs were but don't remember what, MRI and xray of shoulder
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Migraine headaches(PRN meds)
- Andere Medikamente
- Multivitamin
- Allergien
- Sulphur drugs
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 29.05.2022
- Impfdatum
- 25.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Abnormal faeces
Arthralgia
Dyschezia
Haematochezia
Migraine
Muscle spasms
Neck pain
Peripheral swelling
Sensory disturbance
Stomatitis
Tendon pain
Symptomtext
Friday 27 May 2022: Severe Migraine that started at 08:30pm at night. Took naproxen 500. Woke up Saturday 28 May 2022 with migraine. Took naproxen 500mg. At around 4:00 pm started to develop some severe cramps, and abdominal pain. First bowel movement occurred at 6:00pm with strong odor and red bright blood mixed inside each fecal deposit. I had two more painful bowl movements at 7:30pm and at 9:15pm both with red blood. I called man and informed my situation. I was told to go to an urgent care if needed or that I could contact the nurse line. Woke up Sunday 29 May 2022 with abdominal pain, swollen hands and feet and a weird sensation of inflammation on top of my mouth. Also had joint pain in my hands, knees, achiles tendon pain on both feet, and severe neck pain. Developed a severe migraine in the afternoon that still exist up to this point.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- No labs. I have pictures of blood in my stool.
- Aktuelle Erkrankungen
- No illness
- Vorgeschichte
- No long standing health conditions
- Andere Medikamente
- None
- Allergien
- No allergies
- Vorherige Impfungen
- Flu vaccine received in October 2017. Reported to the Hospital with swollen hands and was treated with steroids. I had other inm
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 27.05.2022
- Impfdatum
- 16.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 11,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Facial discomfort
Feeling abnormal
Headache
Hypoaesthesia
Muscle tightness
Musculoskeletal chest pain
Nausea
Pain
Palpitations
Pruritus
Rash vesicular
Scab
Skin lesion
Vision blurred
Symptomtext
She received COVID 19 vaccine #2 on May 16th in her Right deltoid (IM). Patient reports the following post-vaccine #2: During 30 minute wait began to feel "tightness" in face. Waited an additional 40 minutes without progression therefore started to drive home. On the drive home, began to experience "HA, fogginess, R eye cloudy vision sensation" Tightness sensation spread over face (Right) and neck and down chest. Tightness turned to numbness No issues with eating/drinking (swallowing) however doe have some nausea. Went to ED and observed there. Nausea increased however no vomiting. Patient describes severe headache and she was treated symptomatically (Tylenol 975mg, Zofran 4mg). Reassuring exam documented and patient was discharged home. From May 16th (day of vaccine to now) patient reports the following: Numbness sensation on face, neck and down upper right chest has decreased and involved area has decreased/shrinking down to include only her R eye (patient points directly over her globe). Patient does not describe weakness. Headache decreasing in severity and frequency. Using prescribed acetaminophen PRN, which dulls HA to 2/10 (points to entire head) however never fully resolves. Denies sensitivity to light, sound. No vomiting. Left chest wall pain flared to 4-5/10 while exercising (jogging) speed 5 on treadmill for 5 minutes. Experienced sharp/stabbing pain in location of previous pain. With rest, reduced back to baseline 1-2 pain. No associated dizziness, light-headed sensation, SOB, dyspnea. No palpitations during exercise however patient has had palpitations post each vaccine. New rashes developed and areas of previous rash on leg flared. Specifically, rash on left posterior lower leg became fluid filled blister. Developed ~4 lesions on her bilaterally upper extremities on the day of vaccine (May 16th) and continues to have new rashes developing over the past week. Newest lesion is located in the right axillary region; described as itchy and painful 1-2/10. This rash began 3 days ago and has not yet developed a blister. All blisters have started to scab over CURRENT TREATMENT: PRN acetaminophen PRN topical corticosteroid ongoing evaluation with A/I, dermatology, neurology
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no Illness. Did have post-COVID 19 infection symptoms (resp, neuro, cardiac) with normal work-ups
- Vorgeschichte
- denies
- Andere Medikamente
- Xulane transdermal film
- Allergien
- none
- Vorherige Impfungen
- COVID 19 vaccine (Pfizer) #1
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 19.01.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 123,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chronic obstructive pulmonary disease
Condition aggravated
Inappropriate schedule of product administration
Myalgia
Pain
Productive cough
SARS-CoV-2 test positive
Symptomtext
She recieved the first dose Covid on 2/26/21, the second dose on 3/22/21, and the third dose on 1/19/22. She presented ED of Hospital with 3 days of productive cough, body aches, and myalgia on 5/22/22. She was subsecently tested positive for COVID and admitted to manage COVID and COPD exacerbation. She was treated with steroids and Doxycycline. She is on room air during the entire hopsitalization and expected to be discharged on 5/25/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 4,0
- Labordaten
- SARS COV PCR COVID 19 positive on 5/22/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD, CVA, CAD, glomerular low nephritis, CKD
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 10.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Heavy menstrual bleeding
Symptomtext
It made the bleeding worse even more; It made the bleeding worse even more; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-healthcare professional). The reporter is the patient. An 18-year-old female patient received BNT162b2 (BNT162B2), on 10Jan2022 at 10:00 as dose 3 (booster), single (Lot number: FL3209), in right arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE: 1, Date: 16May2021, Time: 3:30 PM, Anatomical site of injection: Right Arm, Batch/Lot number: Pfizer 6W0182), administration date: 16May2021, for Covid-19 immunization, BNT162b2 (DOSE: 2, Date: 06Jun2021, Time: 4:30 PM, Anatomical site of injection: Right Arm, Batch/Lot number: Pfizer 6W0181), administration date: 06Jun2021 for Covid-19 immunization, reaction(s): "Everytime I got up, I would bleed everywhere, legs to floor", "My periods were always bad but never this heavy". The following information was reported: HEAVY MENSTRUAL BLEEDING (medically significant), CONDITION AGGRAVATED (medically significant), outcome "unknown" and all described as "It made the bleeding worse even more". Clinical course: Patient stated her periods were always bad but never this heavy, it all started when she was out in the (state name withheld), where she got her 2nd dose. Every time she got up, she would bleed everywhere, legs to floor and it's so much so fast, the pool cannot hold. When she got my booster, it made the bleeding worse even more. There were no prior vaccinations, Relevant Tests and Specific relevant test for Thromboembolic events with Thrombocytopenia reported. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 20.04.2022
- Impfdatum
- 14.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest X-ray
Cough
Dyspnoea
Feeling abnormal
Headache
Influenza like illness
Pain
SARS-CoV-2 test positive
Symptomtext
I was diagnose with COVID one week after my booster vaccine. I felt flu-ish and I did not feel right. On Friday I got the results that I was positive. I have a cough, persistent, body aches and headaches. X-ray of the chest was performed along with a COVID test. I also had some hard time breathing at night but it seems to have pass. I just haven't felt right ever since getting COVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID test, X-ray of the chest.
- Aktuelle Erkrankungen
- I can really remember; had a sinus infection or cold
- Vorgeschichte
- Idiopathic cyclic neutropenia
- Andere Medikamente
- I take a few prescriptions; Omeprazole; Atorvastatin; Lisinopril; Gabapentin; Paroxetine; I sometimes take Alprazolam; extra strength Tylenol and most recently taking Albuterol Sulfate; Benzonatate
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 20.04.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Heart rate
Heart rate increased
Rash
Symptomtext
This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old male patient received BNT162b2 (BNT162B2), on 14Apr2022 at 14:45 as dose 1, single (Lot number: FL3209) at the age of 56 years, in right arm for Covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Peanut butter Milk" (unspecified if ongoing); "Known allergies: gluten food" (unspecified if ongoing); "If Covid prior vaccination: Yes" (unspecified if ongoing). Concomitant medication(s) included: IBUPROFEN. The following information was reported: DYSPNOEA (non-serious) with onset 14Apr2022 at 16:00, outcome "recovering", described as "Difficult breathing"; HEART RATE INCREASED (non-serious) with onset 14Apr2022 at 16:00, outcome "recovering", described as "Fast heart beat"; RASH (non-serious) with onset 14Apr2022 at 16:00, outcome "recovering", described as "Rash on body all over". The events "fast heart beat", "difficult breathing" and "rash on body all over" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of heart rate increased, dyspnoea, rash. Additional information: No other vaccine in four weeks. Other medications in two weeks included Ibuprofen. No Covid tested post vaccination. Other medical history: Many "concoctions". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220414; Test Name: heart beat; Result Unstructured Data: Test Result: fast.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19; Gluten intolerance; Milk allergy
- Andere Medikamente
- IBUPROFEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 12.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blister
Blood glucose decreased
Blood test
Condition aggravated
Erythema
Fatigue
Hypersensitivity
Influenza like illness
Oral mucosal blistering
Rash
Skin burning sensation
Skin warm
Swelling
Swelling of eyelid
Urine analysis
Urticaria
Vision blurred
Symptomtext
pt states that her sugar level started dropping and her skin felt like it was burning. She felt like she was on fire. She took ibuprofen and then took a norco but nothing helped. She took a shower and noticed she had small cluster of blisters from her eye down her face, in her mouth, on her neck, and on her back. She thought she had shingles. These blisters lasted about 3 days and started to go away but her skin was still burning. She had spots on her skins that would start whelping up into red blisters (the sizes varied from the size of golf balls to the size of baseballs) These spots were swollen, hot to the touch and burning. She developed these spots all over her body including her eyes which she her right eye was blurry and the left eye was swollen shut. This lasted about 4 days. She went to the ER and was prescribed antihistamines. She was told to FU w/ her PCP which referred her to see her dermatologist. She was prescribed multiple strong antihistamines due to having severe allergic reaction. She has had several blood and urine test and has to go back this Monday for further testing. She still has these bumps popping randomly all over her body but they are smaller than they were before. Her sugar level dropped to 30 and stayed under 90 for at least 3 weeks after her vaccine. Her sugar levels are still not normal and she still has blisters 2 months later. She also has continuous interment fatigue and flu like symptoms since this vaccine. 1st Covid Vaccine Pfizer on 4/22/2021 Lot # EW0153 left arm. 2nd Covid Vaccine Pfizer on 5/12/2021 Lot # EW0173 left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- blood and urine test.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- cancer survivor, hypothyroidism, diabetes,
- Andere Medikamente
- metformin 1000mg, levothyroxine 75mg, docusate sodium 100mg, Vitamin B12 1000mg, Vitamin D 5000mg,
- Allergien
- morphine, penicillin
- Vorherige Impfungen
- 1st Covid vaccine she had all over body aches and pain and mild fever with fatigue. 2nd dose covid vaccine she developed nause
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Axillary pain
Balance disorder
Breast pain
Condition aggravated
Decreased appetite
Extra dose administered
Fatigue
Feeling hot
Gait disturbance
Headache
Hyperhidrosis
Immediate post-injection reaction
Injection site pain
Nausea
Pain in extremity
Pyrexia
Tremor
Symptomtext
She got her vaccine, immediately began to feel tired and exhausted. The injection going into her arm was really painful, so her arm is still sore and painful, and she is sore underneath her armpit and down along her side underneath her breast a little bit. She spiked a really temp of 104, and she has been extremely weak, unsteady on her feet, very low appetite and tries to stay hydrated. She does feel a little bit better today and still feels weak and exhausted. She is a fairly active person, does not get sick and cannot tell when she had her lost cold, and really a healthy person. She also has headache, nausea, high fever which has been difficult to keep under control. She has used Tylenol along with cold cloths all over her head, neck, chest, wrists. She is not having a fever at this time, but she has had shakes and feeling of just quivering mostly from weakness. She would start burning out and then pop out with soaking sweats to where she had to change her clothes 2-3 times a day due to it. That has abated at this time, and today when she woke up she felt like maybe she had passed the worst of it. She was too weak to get to the bathroom on her own, which has never happened. She had similar reaction with the third vaccine, but also had the flu vaccine at that time as well, and assumed it was due to those two. She now realizes that this reaction was similar, but this one was worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Diabetes, high cholesterol.
- Andere Medikamente
- Metformin, Crestor, low dose aspirin, Zyrtec.
- Allergien
- Soy, black walnuts, bee stings. Penicillin, and it's derivatives.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 21.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dehydration
Discomfort
Headache
Mobility decreased
Muscular weakness
Thirst
Symptomtext
With the first vaccine, I had fatigue and slept a couple hours, and the second vaccine I developed diarrhea and I couldn't sleep as well which lasted for three to four days. After the booster I have a headache, I took a Tylenol at 9 am and again 12 pm. I sat most of the day, and it felt like my legs were going to buckle underneath me. I found myself really thirsty and I couldn't stop drinking water. I felt very dehydrated. Every movement I made bothered me. After 24 hours my symptoms did go away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- COVID-19 prior to booster
- Vorgeschichte
- Lupus disease, History of Asthma, History, of seizures, Anxiety.
- Andere Medikamente
- Singular, Norco prn, Remeron, Zoloft, Advil Motrin prn, Artificial Tear Eye drops, Senna, Plaquenil, Calcium Carbonate, Keflex, Zyrtec, Pamelor, Omeprazole, Symbicort, VENTOLIN, Lisinopril, aspirin, Lamictal, Imitrex, Zonegran
- Allergien
- Levetiracetam, penicillin, Escitalopram Oxalate, Prochlorperazine, Diphenhydramine Hcl, Ketorolac, Enalapril Maleate - Felodipine, Paroxetine Hcl, Enalapril Maleate, Felodipine
- Vorherige Impfungen
- With the first Pfizer vaccine Lot: EM1202 Date: 02/27/2021 , I had fatigue and slept a couple hours, and the second Pfizer vacci
- Staat
- DE
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Fatigue
Mobility decreased
Nausea
Pyrexia
Vomiting
Symptomtext
I had 103 fever nausea vomiting fatigue weakness and couldn't get out of bed for 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Arthritis; Heart conditions
- Andere Medikamente
- Celecoxib; Hydroxychloroquine; Methylprednisolone; Furosemide; Digoxin; Eliquis; Klor-Con; Omeprazole; Zolpidem; Hydrocodone; Amitriptyline; Metoprolol; Leflunomide
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 02.01.2022
- Beginn
- 02.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Burning sensation
Chills
Cough
Paraesthesia
Symptomtext
cough; Back was hurting and achy; Chills but did not take temperature; Every 2 hours hands will feel tingly and then feel like on fire for 10 minutes and go away; Every 2 hours hands will feel tingly and then feel like on fire for 10 minutes and go away; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program (005570; 159558; 312886). The reporter is the patient. A 43 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 02Jan2022 13:00 (Lot number: FL3209) at the age of 43 years as dose 3 (booster), single for covid-19 immunisation. Family history included: "CML Leukemia" (unspecified if ongoing), notes: Mother had CML Leukemia and not sure if that is relevant, or not. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, single, Lot Number: ER8735, Anatomical Location: Injected in left shoulder), administration date: 11Apr2021, when the patient was 43 years old, for Covid-19 Immunization; Bnt162b2 (Dose 2, single, Lot Number: EW0182,, Anatomical Location: Injected in left shoulder), administration date: 08May2021, when the patient was 43 years old, for Covid-19 Immunization, reaction(s): "After 2nd shot of the Pfizer COVID vaccine, he felt like he got run over by a train and was sick for two days with chills. He did not take his temperature but was achy and his back hurt and that was it."; Bnt162b2 (Dose 2, single, Lot Number: EW0182,, Anatomical Location: Injected in left shoulder), administration date: 08May2021, when the patient was 43 years old, for COVID-19 immunization, reaction(s): "After 2nd shot of the Pfizer COVID vaccine, he felt like he got run over by a train and was sick for two days with chills. He did not take his temperature but was achy and his back hurt and that was it.", "After 2nd shot of the Pfizer COVID vaccine, he felt like he got run over by a train and was sick for two days with chills. He did not take his temperature but was achy and his back hurt and that was it.". The following information was reported: PARAESTHESIA (non-serious), BURNING SENSATION (non-serious) all with onset 2022, outcome "not recovered" and all described as "Every 2 hours hands will feel tingly and then feel like on fire for 10 minutes and go away"; BACK PAIN (non-serious) with onset 02Jan2022, outcome "recovering", described as "Back was hurting and achy"; CHILLS (non-serious) with onset 02Jan2022, outcome "recovering", described as "Chills but did not take temperature"; COUGH (non-serious) with onset 03Jan2022, outcome "recovering", described as "cough". Additional Information: No other relevant medical history. No Additional Vaccines Administered on Same Date of the Pfizer Suspect vaccine considered as suspect. No Prior Vaccinations within 4 weeks of the suspect vaccine. Patient called regarding the Pfizer Booster shot as he had an adverse effect. He got it on Sunday, right after New Year's Eve, and adverse effect was that about every 2 hours, his hands felt tingly and then feel like they were on fire for 10 minutes and would go away. He never had that before. After 2nd shot of the Pfizer COVID vaccine, he felt like he got run over by a train and was sick for two days with chills. He did not take his temperature but was achy and his back hurt and that was it. Every in the morning before - mid-morning around 10:00 am. Back was hurting and achy -22:00-23:00 Chills but did not take temperature 22:00-23:00 Cough -afternoon. It started almost a week after the shot. Also reported as, after getting third shot, he felt that his back really hurt and was achy starting around 10Pm on same evening as shot. He also had chills, but did not take his temperature. He also not sure ended up having a cough. With cough, that did not start until next day in the afternoon. Back hurting and achiness improved after 3 days. He did not have COVID because had to get tested twice weekly at the College, so he wanted to make sure he did not. He had the cough for a month and it started going away. No Emergency Room and Physician Office visit as result of events. Reported that, His girlfriend's daughter had issues with the Pfizer Booster as well. He stated he cannot do report since she is not her daughter. He can have his girlfriend call instead. He did not have a lot or expiration. He did not wish to complete report. He did not have an email for prescriber. No further details provided. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Chronic myeloid leukemia (Mother had CML Leukemia and not sure if that is relevant, or not.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 13.03.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deafness
Hypoaesthesia
Injection site pain
Paraesthesia
Symptomtext
Patient reports severe pain at site of injection, and the next evening had numbness and tingling in left side of neck and inside the ear. The ear continues to feel numb and tingles inside, the neck has now gotten better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Exam did not reveal abnormality. Hearing test reveals loss of hearing 25dbl and 1000Hz bilateral ears
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 14.03.2022
- Impfdatum
- 06.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Hypoaesthesia
Hypoaesthesia oral
Pain in extremity
Paraesthesia
Symptomtext
On the second day of my second Pfizer does, I experienced pins/needle and numbness on my hands, feet and left side of my face/lips. It was been over one month and I am still experiencing these side effects. I went to my doctor, got blood work and it came back fine. I sometime get pain on my hands and feet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Full panel blood work (2/17/2022). Blood work came back fine.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal rigidity
Back pain
Blood pressure increased
Chest pain
Fatigue
Headache
Hypoaesthesia
Muscle spasms
Muscular weakness
Palpitations
Paraesthesia
Peripheral swelling
Symptomtext
Swelling in arm ,fingers, increased blood pressure, chest pain, palpitations, pain and spasm in back, chest, abdomen, numbness and tingling in toes, with cramping, headaches, fatigue, weakness in arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Methylprednisolone, ibuprofen
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension, P. A. D., migraines
- Andere Medikamente
- Clonidine, plavix, labetalol, valsartan, amlodipine,lasix, montelukast, topiramate, treximet
- Allergien
- propofol
- Vorherige Impfungen
- Extreme Fatigue, ,shortness of breath, pain
- Staat
- AZ
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 14.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Depressive symptom
Headache
Migraine
Pain
Suicidal ideation
Symptomtext
Severe Migraines not responding to rescue medication; 10/10 on pain scale; multiple episodes (2-3 per day). Migraines Lasting 1 week in duration; Headaches still on-going. Severe Depressive Symptoms with Suicidal ideation 1 week post-dose. Still ongoing. Initiation of anti-depressant has somewhat alleviated symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Psychiatry consult on 2-23-2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- 02/18/2021
- Staat
- KS
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Throat tightness
Symptomtext
Injection was given and upon standing patient stated she could not breath and her throat was closing. Patient sat back down and EMS were called. Patient never lost consciousness, could always speak, never had any discoloration, and never began to perspire. EMS arrived and accessed patients blood pressure and oxygen saturation. Patient declined to go to the ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD
- Andere Medikamente
- Oxycodone, duloxetine, baclofen, Spiriva
- Allergien
- KNDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Headache
Hypoaesthesia
Paraesthesia
Swelling
Symptomtext
After 2nd shot 3/2021: numbness and tingling in left jaw, neck, shoulder.- resolved by 10/2021. June 2021 sudden fever, upper back pain followed by a series of events with persistent tachycardia. 2/21/22 booster: that evening experienced same numbness, tingling in left jaw, neck, shoulder. Left axillary swelling, mild headache and mild upper back pain (less intense than 6/2021).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- yes. URI 1/7/22. negative PCR x 3. Augmentin, Doxycycline and medrol Dosepak
- Vorgeschichte
- similar reaction after 2nd dose 3/2021. June 2021- severe upper back pain. + elevated D-dimer, interstitial cystitis, right epicondylitis surgery pending, asthma. Persistent tachycardia
- Andere Medikamente
- valsartan, amlodipine, escitalopram, vitamin D3
- Allergien
- gluten meal, lactose, soy
- Vorherige Impfungen
- As above
- Staat
- PR
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Dyspnoea
Headache
Nausea
Pyrexia
Tachycardia
Symptomtext
fever, chills, headache, shortness of breath, tachycardia, dizziness, nausea,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Spiriva Respimat 2.5mcg Breo Elipta 100-25mcg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest pain
Echocardiogram normal
Electrocardiogram normal
Troponin
Symptomtext
4 days after the 2nd dose of the Pfzer vaccine had chest Pain for 2 hours. Patient seen by PMD and sent for Troponin which was mildly elevated, and sent for an ECG at urgent care. Had a normal ECG at urgent care but told to go to the ER. In the ER was well appearing with no chest pain. Had a repeat ECG which was normal. Troponin repeated and very mildly elevated. She was discharged from the ER on Motrin 600mg PO TID, and had cardiology outpatient follow-up set-up within 48 hours with me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Troponin (from ER) 2/12/2022 - 0.09 (0.01 uppper limits of normal) ECG 2/12/22 and 2/14/222 bot normal ECHO 2/14/22 - normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 10.02.2022
- Impfdatum
- 12.04.2021
- Beginn
- 12.04.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Symptomtext
tigling from right knee to groin area
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- amlodepine, losartan, atorvastatin
- Allergien
- -
- Vorherige Impfungen
- Pfizer 4/12/2021 tingling 59
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Mobility decreased
Pain in extremity
Symptomtext
Patient complains of continued arm soreness post-vaccine with some limitation on movement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Discomfort
Feeling abnormal
Hypoaesthesia
Pain
Paraesthesia
Rash
Sleep disorder
Symptomtext
I started feeling ?off? a few hours after vaccine. I had pains traveling throughout my body and was worried it was a blood clot. Later that night, I began feeling pins and needles in my arms, legs, hands and feet which lead to numbness. I continue to have these same symptoms 2 weeks later. They have been getting worse as my whole body is now experiencing numbness (including torso, tongue, gums, face, etc). The tingling and numbness was so bad that i had to pull over when driving. I cannot sleep at night because of how painful and uncomfortable I am. I have been to 2 doctors (PCP and neurologist) and have to undergo further testing. I also developed a large rash on the inside of both legs, both elbows and on my stomach.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Saw PCP on 2/8- gave script for bloodwork. Results WNL. Saw Neurologist on 2/10 - received script for MRI of brain and spine. Currently working on scheduling testing.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest pain
Costochondritis
Electrocardiogram
X-ray
Symptomtext
I was diagnosed with costochondritis , I have a lot of stabbing on my left side in my chest that feel like a heart attack, it hurts all day every day and gets worsen at night to the point I cry myself to sleep.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- ekg , blood test and xray 2-8-22
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Biopsy kidney abnormal
Blood test
Blood urine present
Chromaturia
Hyperhidrosis
Blood glucose increased
Haematuria
Protein total
Proteinuria
Hypertension
IgA nephropathy
Protein urine present
Renal disorder
Thirst
Ultrasound kidney normal
Urine analysis abnormal
Vaccination complication
Urine analysis
Symptomtext
Woke up at 4:00 am with excessive sweat and thirst. Went to the bathroom and noticed my urine was dark brown. It stayed that way all day. The next morning my urine was red so I went to Urgent Care. Urine test showed high levels of blood and protein in my urine. along with high blood pressure which I have no history of having. Was given 2 bags of IV fluids and 5 days of Prednisone. Was told they suspected that the booster shot had triggered a kidney disease called IGA Nephropathy. Followed up with my Primary Care Doctor the next day per the Urgent Cares orders. My Primary Doctor did more urine and blood tests. They did a kidney ultrasound to rule out kidney stones or cysts. Kidney ultrasound was normal. Was referred to a Nephrologist for further evaluation. Was seen by the Nephrologist on Jan 13th for suspected new onset IGA Nephropathy. My kidney biopsy was done on Jan 26th. My results came back and confirmed the diagnosis on IGA Nephropathy. I had no prior history of high blood pressure or any kidney issues/symptoms until 12 hours after I received my booster shot. The covid booster shot triggered this disease in my body and now I will live with this incurable disease for the rest of my life.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Urine and renal bloodwork done on Jan 9, 2022 Urine and renal bloodwork done on Jan 10, 2022 Kidney Ultrasound done on Jan 10, 2022 Urine and full bloodwork done on Jan 13, 2022 Urine and renal bloodwork done on Jan 25, 2022 Kidney Biopsy done on Jan 26, 2022 Urine and renal bloodwork done on Feb 3, 2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Singulair, Junel FE, Albuterol Sulfate inhaler
- Allergien
- Sulphur
- Vorherige Impfungen
- 2nd Covid vaccine made me sick on my stomach and caused me to faint in my bathroom later that evening after receiving it.
- Staat
- NV
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Limb injury
Paraesthesia
Symptomtext
Site: Pain at Injection Site-Medium, Systemic: Tingling (specify: facial area, extemities)-Mild, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Additional Details: Tingling in the arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Dizziness
Ear, nose and throat examination
Mobility decreased
Pain in extremity
Tinnitus
Symptomtext
Could not move my arm due to the severity of the pain, a few hours later started feeling faint and had to lay on the floor so I would not pass out. A day later and since then I have had tinnitus.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- I went to the ENT for the tinnitus and he did an exam and hearing test. 1/27/22.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Zoloft, vivelle dot patch
- Allergien
- no
- Vorherige Impfungen
- 6/18/21 and 7/9/21 Pfizer, sore arm, fatigue, achy.
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Mobility decreased
Symptomtext
patient is having difficult moving arm after vaccine was administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Blindness
Dizziness
Head discomfort
Hypotension
Vomiting
Symptomtext
Once the patient received the vaccine, after 2-3 minutes, he felt dizzy and I asked him to sit down. He went on to say that his head feels heavy and he could no longer see. He drank water and wanted to laid down. Right after he vomited and was escorted by paramedics to the hospital as his blood pressure was very low.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- not that they know of
- Vorgeschichte
- none that they know of
- Andere Medikamente
- none per mom and dad
- Allergien
- not known per mom and dad
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 25,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac monitoring normal
Chest X-ray normal
Electrocardiogram normal
Hypertension
Palpitations
Symptomtext
I had heart palpitation and my blood pressure was high, I was prescribed low dose of BP medication to maintain a decent Blood Pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- 01/31/2022 Chest X-ray, EKG, Heart Monitor results were back normal on all.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Dysphonia
Injection site erythema
Injection site swelling
Injection site vesicles
Injection site warmth
Malaise
Peripheral swelling
Pneumonia
Pyrexia
Vaccination complication
Symptomtext
That night I got sick and coughed, and my voice changed. I took Nyquil, my cough subsided but I had a fever all night. The next day my arm was swollen (COVID arm). The 1/8 had a circle around the vaccine, red and hot. Two days later the arm was spreaded and grew around it. My fever (97.3) went away and my friend recommended Levothyroxine 5 mg, one every 24 hours for 5 days and my arm got better. A week later it changed color (from red to brown) and on January 15 it was still swollen. Two days later (1/17) the color turned into blisters with water. I popped them and the skin started to change and the swelling went down. I have a little swollen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mental(depression), First in the ovaries, pulmonary scar.
- Andere Medikamente
- None
- Allergien
- Shrimps, bees
- Vorherige Impfungen
- Yes. Pneumonia (pneumococcal), 14 yrs old.
- Staat
- CT
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Impaired work ability
Incorrect dose administered
Migraine
Nausea
Product preparation issue
Vomiting
Symptomtext
Clinician prepared vial with 1.3ml Normal Saline diluent rather than 1.8ml Normal Saline. During conversation of being notified of VAERS report she reported experiencing Nausea & vomiting with a migraine evening after injection. She stated she missed 3 days of work. Reports feeling well now with no clinical concerns
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Pyrexia
Wheezing
X-ray
Symptomtext
A day after the booster he had a fever of 102. The day afterward, he developed a slight wheeze. (Sunday) We went to the Dr on Monday and he was given a steroid. He went back to the Dr the following Thurs and they did a dual-neb and x-ray. The wheezing and shortness of breath stopped a week later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Sinus infection 2 weeks prior to booster
- Vorgeschichte
- Asthma
- Andere Medikamente
- Symbicort inhaler, Xertec, Montelukast, Hydroxafine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 01.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Migraine
Symptomtext
I had the traditional headache that you get with the vaccine but it has turned into daily migraines that won't go away with any medication. Its extremely disruptive to my daily activities and I never suffered from even a headache on a regular basis like this before I got vaccinated. The headache started within the hour of my second shot on January 9th 2022. Today is February 1st, so almost a month later and im still suffering from daily migraines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Fibromyalgia, colitis
- Vorgeschichte
- Asthma, fibromyalgia, colitis, scoliosis
- Andere Medikamente
- Daily multivitamin, gabapentin 300mg
- Allergien
- No allergies
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Chills
Fatigue
Feeling abnormal
Headache
Heart rate increased
Hypotension
Myalgia
Nausea
Palpitations
Pyrexia
Symptomtext
Extreme sudden onset fatigue, fever of 101.2, chills, joint and muscle pain throughout, nausea, headache, sensation of heart pounding, HR elevated from my baseline of low to mid 80s bpm, although still wnl (93-97bpm and regular). My baseline HR of 80s is due to being 30lbs overweight at this time. When at my normal weight, HR is in 60s-70s. Sensation of being in a fog, difficulty retaining simple self-test at home Covid-19 antigen rapid test instructions, needing to go back to instructions over and over. O2 saturation is 99% according to my home pulse oximetry. Rapid test was negative. I also feel like my BP might be low, but can't seem to get the cuff on due to the severe fatigue and weakness. No one available to do it for me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 24.01.2021
- Beginn
- 30.01.2022
- Tage bis Beginn
- 371,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Decreased appetite
Dyspnoea
Dyspnoea exertional
Fatigue
Symptomtext
Pt has COPD and is on 3L NC with former tobacco dependence. She has had increased shortness of breath with activity, fatigue, generalized weakness, and loss of appetite.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Injection site reaction
Rash erythematous
Rash pruritic
Lethargy
Mobility decreased
Muscle fatigue
Symptomtext
On 1-31-22 the patient called to notify the pharmacy that she developed a mild rash with redness and itchiness at the injection site after receiving her third dose of Covid Pfizer vaccine on 1/27/22. She was unsure if there were any lymph node involvement under her arm. She asked about what she could take temporarily to relieve the mild itching. She said she was not allergic to Benadryl. I recommended Benadryl 25 mg 1 or 2 capsules or tablets by mouth, warned her about sedation, not driving and not to take any alcoholic beverages. I advised her to seek for medical attention ASAP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Injection site reaction
Rash erythematous
Rash pruritic
Lethargy
Mobility decreased
Muscle fatigue
Symptomtext
On 1-31-22 the patient called to notify the pharmacy that she developed a mild rash with redness and itchiness at the injection site after receiving her third dose of Covid Pfizer vaccine on 1/27/22. She was unsure if there were any lymph node involvement under her arm. She asked about what she could take temporarily to relieve the mild itching. She said she was not allergic to Benadryl. I recommended Benadryl 25 mg 1 or 2 capsules or tablets by mouth, warned her about sedation, not driving and not to take any alcoholic beverages. I advised her to seek for medical attention ASAP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 29.01.2022
- Impfdatum
- 29.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hypotension
Pallor
Symptomtext
Patient got light headed with signs of low blood pressure due to vaccine and pale skin. Patient was asked to be in pharmacy for 20 minute after vaccination in case of side effects. Patient mentioned that he did not have breakfast and he was provided with water. After 5 minute he was feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hypoaesthesia
Hypoaesthesia oral
Paraesthesia
Paraesthesia oral
Pharyngeal hypoaesthesia
Pharyngeal paraesthesia
Symptomtext
Numbness and tingling in right hand and arm of injection site. Numbness and tingling of mouth, throat, and tongue. Lightheadedness/Dizziness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Vital Signs-1/28/2022
- Aktuelle Erkrankungen
- Multiple Sclerosis
- Vorgeschichte
- -
- Andere Medikamente
- albuterol HFA (VENTOLIN; PROAIR; PROVENTIL) 90 mcg/actuation aerosol inhaler albuterol nebulizer solution 2.5 mg 2.5 mg, Nebulization, Every 6 hours PRN cholecalciferol, vitamin D3, (VITAMIN D3) 2,000 unit cap 2,000 Units, Dail
- Allergien
- Cephalexin Amlodipine Cefprozil Chlorthalidone Lisinopril Metoprolol Cefuroxime Axetil Diltiazem Hydralazine : Hydrochlorothiazide
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lethargy
Lymphadenopathy
Migraine
Muscle spasms
Nausea
Pain
Pyrexia
Symptomtext
Just this time: cramping, nausea, fever, swollen left lymph (in the armpit area), body aches, lethargy and migraines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hashimoto's, hypothyroidism
- Andere Medikamente
- Levothyroxine, Acetaminophen, prenatal vitamins, Vitamin D
- Allergien
- Soy, pecans and Aspirin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Palpitations
Symptomtext
However about 16 hours after my booster I also had chest pain and heart palpitations, which I have never had from a vaccine before; However about 16 hours after my booster I also had chest pain and heart palpitations, which I have never had from a vaccine before; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 28 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 08Jan2022 10:30 (Lot number: FL3209) at the age of 28 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "IBS" (unspecified if ongoing). Concomitant medication(s) included: LAMOTRIGINE; FLUOXETINE. Vaccination history included: Bnt162b2 (prev dose product: COVID 19, prev dose brand: Pfizer/ Biontech, prev dose brand unknown: False, prev dose lot number: FE3380, prev dose lot unknown: False, prev dose administration date: 11Aug2021, prev dose administration time: 02:00 PM , prev dose dose number: 2, prev dose vaccine location: Left arm), administration date: 11Aug2021, when the patient was 28 years old, for covid 19 immunization, reaction(s): "For the first two doses I had a sore arm, which I expected"; Bnt162b2 (prev dose product: COVID 19, prev dose brand: Pfizer/Biontech, prev dose brand unknown: False, prev dose lot number: FA1027, prev dose lot unknown: False, prev dose administration date: 16Jun2021, prev dose administration time: 08:45 AM , prev dose dose number: 1, prev dose vaccine location: Left arm), administration date: 16Jun2021, when the patient was 28 years old, for covid 19 immunization, reaction(s): "For the first two doses I had a sore arm, which I expected". The following information was reported: PALPITATIONS (non-serious), CHEST PAIN (non-serious) all with onset 09Jan2022 02:00, outcome "recovered" and all described as "However about 16 hours after my booster I also had chest pain and heart palpitations, which I have never had from a vaccine before". Therapeutic measures were not taken as a result of palpitations, chest pain. There were no other vaccine in four weeks. There was no covid prior vaccination. Covid was not tested post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Irritable bowel syndrome.
- Andere Medikamente
- LAMOTRIGINE; FLUOXETINE.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Chills
Dyspnoea
Feeling cold
Nausea
Pyrexia
Tremor
Symptomtext
Nausea - From time of injection to end of day (approx. 9:45 am - 11:00 pm) - Mild Chills, feeling feverish - About 3-4 hours after injection, noticed around 1:00 pm. Mild at this point. Felt slightly cold, a little shake. At approx. 5:00 pm, symptoms steadily worsened, to the point of being unable to hold objects nor perform basic tasks such as writing. I was unable to warm myself, even when wearing a winter jacket to bed under layers of blankets. This continued into the next day after I'd slept, though not as bad as the night before. The next morning (approx. 8:00 am), I was shaky, but still able to hold objects and write steadily. I was no longer feeling cold in the morning. Breathing difficulties - pains in chest. Still present, off and on. Mild (as of now). On day of injection/dose, occasional pangs of pain in chest area- moderate pain for approx. 36-48 hours after injection/dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic Migraines
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Dizziness
Hypotension
Hypotonia
Symptomtext
Patient vaccinated t 11:30 am. At 11:33 I gave her a photocopy of her vaccine record and she told me she felt lightheaded. I offered her cold bottled water which she took and also offered to raise her legs onto a 2nd chair which she did not want to do. At 11:40 am 2nd RPh on duty was called to the front lobby - patient was slumped over onto a 2nd chair. Rph raised patient's legs onto chair, waited with patient in lobby then asked me to assist her with getting patient into counsel room and elevating legs again. Rph took BP - 78/49 I requested patient call someone, remain seated with legs up, and we would retake BP. Rph stayed with patient, redid BP at 11:46, was 104/60 Patient said she normally runs low and she gets lightheaded easily, but felt much better. She went to sit in the lobby a few minutes later. I checked on her at 11:58 am and patient was standing - said she felt much better and was going to go home. She left.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- BP first read 78/49 second reading 104/60
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- no known allergies per her profile
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Chills
Laboratory test
Pyrexia
Tachycardia
Symptomtext
Chills, Fever, Tachycardia and raised blood pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- Yes
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dizziness
Dyspnoea
Palpitations
Vision blurred
Visual impairment
Symptomtext
Client reported dizziness to EMT. The client ambulated and sat down in the anti-gravity chair. The anti-gravity chair was reclined to a semi-fowler's position. Lead RNs responded. The client reported blurry vision, dizziness, and chest pressure. The client reported that he has been experiencing chest pressure and body aches for the last few days. The client also stated he felt he was, "not able to fully fill my lungs." Vitals obtained at 11:56AM were as follows: BP 122/70, HR 88, O2 99%. The client stated his chest pressure was currently at a 7 on a 10 point scale. The client started drinking water. The client stated the chest pressure has been at a 6/7 out of 10 the last few days. The client stated the chest pressure has been intermittent over the last few days and that sitting makes it worse. The client denies any current medications, chronic conditions, or known allergies. The client stated his symptoms were "getting a little better." The client stated he did eat about one hour before coming to the vaccination site but has not consumed any water today. The client reported "trouble focusing" his vision. The client also stated that his dizziness was a little better. Repeat vitals obtained at 12:02PM were as follows: BP 118/66, HR 93, O2 99% The client reported that his chest pressure was "a little better" and rated it at a 3/10. The client stated his breathing was "better." The client stated his dizziness was going away. The client denied any other signs or symptoms of anaphylaxis. Repeat vitals obtained at 12:07PM were as follows: BP 122/60, HR 88, O298%. The client was sitting in a high fowler's position. The client stated the dizziness was at a 2/10 and "still there a little bit." The client declined any snacks. RN provided education regarding possible adverse reactions, when to seek care, and V-Safe. RN also recommended the client follow up with a primary care physician regarding his ongoing chest pressure. The client voiced understanding of this education. RN provided the client a list of community clinics. The client reported a history of anxiety and stated he "sort of had the same chest pressure before." Vitals obtained at 12:17PM were as follows: BP 124/62, HR 68, O299%. The client stated the dizziness was at a 1/10 and that he was able to focus his eyes. The client also stated he has been experiencing palpitations over the last few days and is experiencing some now. RN noted lungs clear to auscultation and no gallups, rubs, or murmurs noted. The client stood up unassisted and denied any current dizziness. The client stated he "felt normal." The client stated his mother was driving him home. The client ambulated unassisted with a steady gait out of the vaccination site at 12:26PM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Anxiety
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest discomfort
Dyspnoea
Electrocardiogram abnormal
Fatigue
Pyrexia
Tachycardia
Symptomtext
Directly after my vaccine, having a history of a anaphylactic reaction to Moderna vaccines. After injection with Pfizer vaccine, I sat down and was much more relaxed and felt like I had pressure on my chest causing difficulty breathing. Doctor came in checking vitals and administered epinephrine, ambulance came in and checked vitals and administered Benadryl and steroids in transit to ER, ER did an EKG and waited for the symptoms to lessen. Now I am just experiencing heavy fatigue, and tachycardia that lasted for a few days post ER visit, and slight fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- EKG showed Tachycardia
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- Mild persistent asthma; hypertension; fibromyalgia
- Andere Medikamente
- Metoprolol; asthma meds; KYLEENA
- Allergien
- Amoxicillin; CELEXA; latex; sulfa; VICODIN
- Vorherige Impfungen
- Moderna Dose#2, 05/03/2021, E-Report: 001C21A.
- Staat
- PA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Dyspnoea
Headache
Hyperhidrosis
Hyperventilation
Insomnia
Pyrexia
Wheezing
Symptomtext
The patient had difficulty sleeping due to headache, fever, sweating. When she got up in the morning, she had a sudden, severe breathing event with rapid hyperventilation, and an inability to draw air into her lungs. She was gasping/weezing for breath. I worked with her to slow her breathing and regain control but the incident lasted several minutes. After it subsided, we provided advil for the fever/headache and she was able to sleep until 2pm. when she woke she felt better and had mild tightness in her chest, with continued more mild headache through Monday. No additional breathing incidents to date. The event was reported to her doctor via phone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- social anxiety
- Andere Medikamente
- none
- Allergien
- allergic to many tree fruits
- Vorherige Impfungen
- mild typical symptoms after 2nd covid shot
- Staat
- -
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 23.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypersensitivity
Injection site urticaria
Throat irritation
Throat tightness
Tremor
Urticaria
Symptomtext
Patient received her second dose Pfizer COVID vaccine (Lot#FL3209 exp: 06/30/2022) on 1/23/22. Patient alerted RNs and stated she felt tightness in her throat and was shaking a lot. Patient was accompanied by her Grandma. Grandma stated that patient had finished her 15 minute observation and as soon as they got in the car patient stated that her throat "felt weird." Grandma then decided to bring patient back to vaccination site from their car. RN took patients vital signs at 1222. BP: 146/84, HR: 84, O2: 98%. Patient stated her "throat felt weird." RN retook patients vital signs and reassessed patient at 1227. BP: 137/82, HR: 105, 02: 99%, RR: 16. Patient was shaking and there was noticeable hives around the injection site on left arm and on the left side of her neck. Patient stated that she felt her "throat was tight." RN assessed patients respiration rate at 1231 RR: 16. RN called EMS at 1227. RN called Vaccine Operation Lead asked if it was okay to give minor Benadryl without parent present. RN asked RN to get parent verbal consent for approval of Benadryl IM administration. Verbal consent to give Benadryl IM was given by Father for patient over facetime to RN at 1233. Patient stated she weighed 48 kilograms (105 lbs). With client's assent, RN gave patient IM Benadryl (LOT#: 041020 exp: 04/23) in the right deltoid at 1233 (1mL (50mg) as directed in emergency protocol for patients >45 kilograms). RN retook patients vital signs at 1234. BP: 135/93, HR: 98, O2: 98%, RR:16. EMS arrived at 1235 and assumed care. EMS assessed patient and recommended that patient go to hospital since parent guardian wasn't on site. Grandma called patients father via facetime and he stated he did not want his daughter going to the ED. EMS had to receive Physician approval for AMA. Paramedics educated father on worsening signs and symptoms of allergic reaction and recommended that patient go to ED as soon as possible. Father of patient verbalized understanding and stated he would take daughter to ED. Physician from local hospital gave consent to release patient to grandmas care. EMS left vaccination site at 1246. RN retook patients vital signs at 1302. BP: 134/83, HR: 123, O2: 99%, RR:16. Patient stated she had not eaten anything all day. Patient was given a juice, water and crackers. Patient finished her snack. Patient stated that she was feeling a lot better and that symptoms had subsided. Patient completed 30 minutes of extra observation at 1303. Patient stated that she was feeling "a lot better" and symptoms had completely subsided. RN educated patient and her Grandma on worsening sign and symptoms of COVID vaccine and when to seek EMS. RN educated patient and her Grandma on worsening signs and symptoms of an allergic reaction and recommended patient go to ED as soon as possible. Patient and Grandma verbalized understanding. Grandma stated that she "was going to take her granddaughter to her Dad's and then he was going to take patient to the ED." Patient left vaccination site with a steady gait and unassisted with her Grandma at 1305.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dyspnoea
Oxygen saturation decreased
Symptomtext
Soon after receiving the vaccine, patient communicated to caregiver that she was having difficulty breathing. This continued to occur, I administered an epipen. I called for paramedics to come. Her pulse ox was low when I checked but improved to normal when paramedics arrived. Caregiver stated she may have been having a panic attack. Paramedics decided to take her to hospital for observation due to difficulty breathing. I called caregiver the following day- patient was discharged previous night and doing ok.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- seizures, emotional seizures, high cholesterol, hypertension, hypothyroidisim, diabetes, glaucoma
- Andere Medikamente
- Atorvastatin, Calcium carbonate, amlodipine, klonopin, brimonidine eye drops, depakote, Diastat rectal gel, Januvia, latanoprost, metformin, Timolol eye drops, Ergocalciferol, Lamictal, levothyroxine, Iron complex
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Mobility decreased
Symptomtext
Severe flare up of arthritis in hip and knee causing extreme pain and mobility.; Severe flare up of arthritis in hip and knee causing extreme pain and mobility.; Severe flare up of arthritis in hip and knee causing extreme pain and mobility.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 46-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 06Jan2022 16:15 (Lot number: Fl3209) at the age of 46 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "known allergies: Sulfa medicine" (unspecified if ongoing). There were no concomitant medications. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. The following information was reported: ARTHRITIS (non-serious), MOBILITY DECREASED (non-serious), ARTHRALGIA (non-serious) all with onset 08Jan2022 16:15, outcome "not recovered" and all described as "Severe flare up of arthritis in hip and knee causing extreme pain and mobility". Therapeutic measures were not taken as a result of Severe flare up of arthritis in hip and knee causing extreme pain and mobility. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Sulfonamide allergy.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Chest discomfort
Chest pain
Decreased appetite
Dyspnoea
Hypophagia
SARS-CoV-2 test positive
Symptomtext
CHIEF COMPLAINT: presents to ED with complaints of increased sob. states covid + a week ago. HISTORY OF PRESENT ILLNESS: 72-year-old male with a history of hypertension and prior CVA presenting for evaluation of shortness of breath and chest pain. Patient states that he received his COVID booster shots last Tuesday. Last Thursday, he does positive for COVID-19. He reports shortness of breath, generalized weakness, poor appetite, and chest tightness. He denies fevers or chills. He reports poor p.o. intake. Denies leg swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Gout, Hypertension, Hyperglycemia, Hypothyroid, Prediabetes
- Andere Medikamente
- Unknown
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate increased
Injection site swelling
Tachycardia
Urticaria
Symptomtext
Large welt and swelling at injection site 3 x 3 inches, rapid heart rate (tachycardia 100+ bpm)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- PCP's office informed
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- fibromyalgia
- Andere Medikamente
- cymbalta, crestor
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram
Electrocardiogram ambulatory
Fatigue
Palpitations
Symptomtext
After a period of about 30 hours of feeling completely knocked out and in bed, with no fever, sore throat or muscular aches, just felt very tired, I started feeling my heart pounding very strongly while in bed or horizontal position. The feeling persisted, though I feel it is subsiding. Notwithstanding, I did go to my cardiologist and had an EKG holter installed and measures taken, I handed that holter today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- An EKG holter was put on me for 24 hours, I handed that holter back this morning, I do not know about the results yet.
- Aktuelle Erkrankungen
- None that I know of...
- Vorgeschichte
- Chronic Rhinitis
- Andere Medikamente
- Crestor 5 Mg, daily
- Allergien
- Benadryl
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysphagia
Dyspnoea
Eye swelling
Mouth swelling
Paraesthesia
Pruritus
Swelling face
Swollen tongue
Throat tightness
Symptomtext
Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Medium, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Crying
Dizziness
Screaming
Tachycardia
Symptomtext
The patient was administered her first dose of the Pfizer Covid vaccine by our pharmacy intern. She was instructed to wait 15 minutes in the store before leaving. Towards the end of her observation period, a woman came to the pharmacy counter screaming and crying for help. We instructed someone to call 911, I grabbed an epi-pen, assessed the situation, and administered it into the patient in right thigh. She started to become alert and responsive. The patient described dizziness and tachycardia as her main symptoms. Once she was alert, we gave her water and observed her until the paramedics came.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test normal
Chest X-ray normal
Chest pain
Headache
Heart rate increased
Hyperhidrosis
Hypertension
Myalgia
Sleep disorder
Symptomtext
Thurs (1/13/2022) afternoon, my son received a booster shot. Friday, he complained of headache and muscle soreness from his shoulder to his knee. On Friday night, he started having chest pains, high heart rate, sweats. Saturday morning, he told us, his parents, about the chest pains and that it hurt badly enough to keep him awake all night. I took his bp, temp and heart rate. bp was high, temp was 99.3, heart rate was 120. We contacted his pediatrician who recommended we go to an ER with imaging. We went. My son's father has a clotting disorder, that was disclosed at the ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Blood tests, chest xray. 1/15/2022. All within normal ranges. Myocarditis was ruled out and we were sent home. Symptoms were gone by Sunday (1/16/2022) afternoon. This was a very expensive vaccination for us as ER visits are expensive and we really needed to have him seen for this, being chest pains.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin C
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Chest discomfort
Confusional state
Immunisation
Insomnia
Palpitations
Stress
Weight decreased
Symptomtext
This is a spontaneous report received from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 52-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 08Jan2022 at 18:00 (Lot number: FL3209) at the age of 52 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: Factor IV and "Fruit allergy" (unspecified if ongoing), notes: Mango (skin contact only). Concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: FL3209, Route of Administration: unspecified, Administration Time: 05:30, Anatomical Location: Left arm), administration date: 16Apr2021, when the patient was 52 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: EW0170, Route of Administration: unspecified, Administration Time: 17:30, Anatomical Location: Left arm), administration date: 07May2021, when the patient was 52 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 08Jan2022 at 18:00, outcome "unknown", described as "Dose number: 3"; ANXIETY (non-serious) with onset 09Jan2022 at 18:00, outcome "recovering", described as "24 hours after the shot, began feeling anxiety. Continued so far for 5 days (better on day 5 (today is day 5), not great)"; INSOMNIA (non-serious) with onset 09Jan2022 at 18:00, outcome "recovering", described as "Sleeplessness"; PALPITATIONS (non-serious) with onset 09Jan2022 at 18:00, outcome "recovering", described as "Heart palpitations"; CONFUSIONAL STATE (non-serious) with onset 09Jan2022 at 18:00, outcome "recovering", described as "Mind going wild"; CHEST DISCOMFORT (non-serious) with onset 09Jan2022 at 18:00, outcome "recovering", described as "Tightness in chest"; WEIGHT DECREASED (non-serious) with onset 09Jan2022 at 18:00, outcome "recovering", described as "Resulted in weight loss"; STRESS (non-serious) with onset 09Jan2022 at 18:00, outcome "recovering", described as "Very stressful". Therapeutic measures were not taken as a result of anxiety, insomnia, palpitations, confusional state, chest discomfort, weight decreased and stress.Additional Information: Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. : It was reported that the patient had not recovered yet and will probably seek medical treatment if continues or worsens The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Fruit allergy (Known allergies: Mango (skin contact only.))
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Cardiac flutter
Cold sweat
Condition aggravated
Dyspnoea
Symptomtext
Patient Received her booster dose Pfizer vaccine (LOT#: FL3209) at 1527 on 1/16/22. Patient alerted EMT's at 1549 that she felt short of breath, cool and clammy and felt her "heart fluttering" a little after getting vaccine for about 5 minutes. Patient alerted EMT's after most symptoms had subsided. Patient stated that she felt weak. Patient was moved to anti-gravity chair. EMT took patients vital signs at 1549. BP: 124/76, HR: 99, O2: 99%. RN arrived on scene at 1551. Patient stated that she felt weak, no SOB, no irritation in the throat. Patient stated this has happened in the past as far as her heart fluttering. Patient has seen PCP about this issue back in July 2021. EKG was taken and patient states everything is normal. EMT retook patients vital signs at 1557. BP: 122/73, HR: 86, O2: 100%. Patient stated she is feeling better and all symptoms have subsided. EMT retook patients vital signs at 1611. BP: 120/74, HR:76, O2: 100%. Patient reports no new symptoms. EMT reassessed and retook patients vital signs at 1622. BP: 118/74, HR: 76, O2: 100%. Patient did not report any new symptoms. RN educated patient on side effects of COVID vaccine and when to seek help from EMS. RN also recommended that patient go see PCP once again for her heart fluttering issue. Patient verbalized understanding. Patient completed her 30 minute observation and left vaccination site with a steady gait with her aunt at 1623.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Chest pain
Injection site pain
Pain in extremity
Paraesthesia
Swelling
Tenderness
Symptomtext
The sore arm commenced about 7.5-8 hours after injection (just like previous 2 vaccines, which were also Pfizer), however the upper & under upper arm areas from my left shoulder to my left elbow became extremely sore with tingling in left thumb. The very significant pain in the left underarm pit commenced about 0130 hours then spread down the left side of my chest to the left breast area but didn't go into the breast. This is also when the swelling of that whole area started. The swelling was about 6"long x about 3" wide x about 2.5-3" high. The pain in this area required me to live around the clock on acetominophen for 3 days and I couldn't wear my usual bras. I looked like a water balloon had been inserted under my skin in this swollen area - the area was very tender, sore. I also slept 14 hrs/day for the 1st 2 days of the vaccine, which is what also happened with the 1st 2 vaccines. The usual achy/sore back lasted the usual 2-3 days, and the decrease in appetite lasted the usual 2-3 days. The swelling is still present but is gradually subsiding; wearing my normal bras is still not feasible. I was able to stop taking the acetominophen on day 4. I'm VERY concerned about this swelling as a side effect, and hope no further Covid vaccines/boosters are recommended for me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None - emailed my internist 1/16/22 with these side effects
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acid Reflux, borderline diabetes but not on any Rx since not actual diabetic
- Andere Medikamente
- OTC Probiotic, L-Glutamine, Vitamin D
- Allergien
- Allergic to Sulfa, Erythromyacin, Cleocin, Percocet, Codeine, Dilaudid, Clindimyacin
- Vorherige Impfungen
- 3/19/21-Pfizer vaccine #1; age 61 yrs - sore arm, decreased appetite, slept 14 hrs/day for 2 days; 4/9/21-Pfizer vaccine #2, age
- Staat
- MN
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphthous ulcer
Bacterial test negative
Condition aggravated
Fatigue
Headache
Herpes simplex test negative
Lymphadenopathy
Pain
Pruritus
Pyrexia
Smear vaginal normal
Vaginal ulceration
Vomiting
White blood cell count abnormal
Symptomtext
-Patient developed three ulcerous lesions (similar to canker sores) in her vaginal area. One was a little larger than a pencil eraser and the other couple were smaller. They were itchy and painful. She noticed them on Sunday and we went to her medical provider on Wednesday. As of today, 1/17/2022, they are getting better and resolving but they have not yet healed completely. She has never had these before in her genital area and did not have this reaction after her first or second doses. There was no recommended treatment. -Patient's lymph node in her left armpit became swollen and noticeable on Saturday afternoon, 1/8/2021, maybe around noon. This was a new symptom which she did not experience after the first or second doses. -She had one canker sore in her mouth at the same time. New symptom. -Her reaction after her booster also included a fever of 101.3, fatigue, vomiting, headache and bodyaches. This started around 05:00am on Saturday, 1/8/2021 and lasted until about 9:00 pm on Saturday 1/8/2021. Since she had a fever, vomiting, fatigue and aches after her second dose, we anticipated these symptoms after booster. We treated her symptoms with Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Wet Prep (Collected: 1/12/2022 12:17 PM) Results Value Ref Range Fungal Elements Not Detected Not detected Clue Cells Not Detected Not Detected White Blood Cells Detected (A) Not Detected Trich Vaginalis Not Detected Not detected Herpes Simplex Virus PCR (Blood, Amnio, BAL and Tissue sources) (Collected: 1/12/2022 12:17 PM) Result Value Ref Range Herpes Simplex Virus by PCR Not Detected Herpes Simplex Virus Source Tissue
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Clindamycin topical lotion, tretinoin cream, women's multivitamin
- Allergien
- Amoxicillin, sulfa meds
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Disturbance in attention
Dysstasia
Feeling abnormal
Feeling hot
Gait inability
Injected limb mobility decreased
Injection site swelling
Lymphadenopathy
Migraine
Pain
Sensory disturbance
Somnolence
Symptomtext
The shot was given at 0130pm on Jan 13. Symptoms woke me up at 0130am on Jan 14th. Chills that were not helped by putting multiple blankets and or clothes on. Unable to get up and walk, tried to put weight on legs felt like they were breaking, inflammation in the left armpit lymph nodes. noticed a small swell at the shot site that I thought was normal. But the swelling in the armpit/ node area hindered the movement of my left arm. Needed support getting to the bathroom ( I am fully capable of reaching the middle of my back and going to the bathroom by myself on a regular day) I reported similar symptoms to my primary care MD when I received the 2nd dose of Pfizer Biotech Lot EL3302 given at the hospital I work at on 1/27/2021. I did not realize I could self-report at that time otherwise I would of. I have all of those symptoms written down if they are needed. The major difference between that time and this time is that after 4 days I still currently have limited mobility in my left arm due to the swelling in the armpit/nodes. The hospitals are crazy right now and I am also trying to get a response from my primary care to see what to do next. I experienced chills for 48 hours. I then was extremely hot for 24 hours. I was groggy ( unable to focus and was abnormally very upset) and had severe pain all over my body. A migraine type of headache started on Saturday jan15th. I took Imitrex to try and relieve that. I took 2 x200mg ibuprofen w/ 1 500 mg Tylenol trying to help relieve the symptoms. It did not help much. I honestly thought the reaction to the seconnd shot would not happen on the third shot. Because on the first shot I had no issues. I obviously was wrong. I want to report these symptoms to try and help studies. Maybe it is because I have no Thyroid. I am not sure but this is awful and I will be refusing any future COVID vaccines this is dangerous, unfortunately.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- Waiting for primary doctor to get back to me.
- Aktuelle Erkrankungen
- Hypothyroidism
- Vorgeschichte
- Hypothyroidism, due to thyroid cancer in 2012.
- Andere Medikamente
- at 0500 am Levothyroxine 150mcg was taken.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Palpitations
Symptomtext
Pt got lightheaded and felt like his heart was racing about 5 minutes after the vaccine. The effects went away pretty quickly. Pt sat in lobby about 30 minutes and had no symptoms at time of departure. Checked in with pt at the end of the day and he was feeling fine and had no symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- Almonds
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Lymphadenopathy
Mobility decreased
Pain in extremity
Swelling
Tenderness
Symptomtext
Pt got vaccine in afternoon. Awakened next morning unable to move the arm in extreme pain. Examined in office and even with max OTC meds on board (Ibuprofen and Acetaminophen) she was incredibly tender to the touch, mildly swollen and unable to abduct the arm at the shoulder. No nerve symptoms. Pain has persisted and now the patient has shoulder pain on that side and very enlarged nodes under the arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Headache
Oropharyngeal pain
Pyrexia
Sneezing
Tachycardia
Symptomtext
Headache, tachycardia, fever, sore throat, cough, sneezes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Taking collagen, colostrum.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Arthralgia
Blood test
Electrocardiogram normal
Headache
Heart rate irregular
Hypertension
Mobility decreased
Nausea
Tachycardia
Tremor
Symptomtext
On the day of January 7, 2022 started having headaches, shaking, abnormal heart beats. I stayed in the bed most of the day for Fri-Sun. I was experiencing abdominal pain, joint pain, nausea. On Monday I contacted my doctor called me in for a physical exam and discussed my symptoms and my blood pressure was high on that visit. I went for blood work on January 13, 2022 waiting on results and have a appt scheduled with the Cardiologist for Tachycardia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- EKG (normal), Bloodwork (waiting results)
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Anemia
- Andere Medikamente
- Iron supplements, Vit D
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dry mouth
Dysphagia
Dyspnoea
Fatigue
Fear
Headache
Heart rate increased
Injection site pain
Pain
Sensation of foreign body
Vaccination complication
Symptomtext
30 minutes after vaccine I started getting a very dry mouth, had a feeling of difficulty swallowing, felt like a lump in the throat, breathing required more respiratory effort the normal. I placed a pulse ox on my finger, the heart rate was 120, but oxygen saturation was 99%. I monitored the pulse ox which remained stable at 99%. The symptoms decreased after 2 hours. Followed by body ache, chills, headache , fatigue and soreness at injection site. I was afraid to sleep by myself that night afraid my throat would close up so my mother watched me all night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- I notified my doctor the next day. which they are referring me to an allergist. Which seems stupid since this is an adverse reaction not an allergic reaction.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- mild asthma-stable exercise induced.
- Andere Medikamente
- minocycline for acne
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Child maltreatment syndrome
Dehydration
Fatigue
Injection site pruritus
Neck pain
Pruritus
Somnolence
Symptomtext
Jan. 8 - sharp pain in the left side of neck itching at the injection site and down the left side of the body near the left breast, left side of belly and hip, thigh, and knee, and at the left crease of the knee. Very tired. Jan. 9 - Left shoulder pain and the left side of neck, very tired. Jan. 10 - sore shoulder and neck left side only. Very tired and sleepy, slept 22 hours, every time I awoke I was still very sleepy and fell immediately back to sleep Jan. 11, - Excessive sleep and feeling dehydrated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- Appointment set for 1/13/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- right leg pain and swelling, hemorrhoids, sinus allergies, PTSD, depressive disorder
- Andere Medikamente
- vitamin D, multivitamin, B-12, biotin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Hypoaesthesia oral
Swollen tongue
Throat irritation
Symptomtext
Client reported to on site EMS approximately 5:25 pm numb feeling of the mouth and tongue feeling swollen and difficulty breathing. Client alert and oriented, was able to communicate and answer questions. On site EMS assessed client, vitals taken, all vitals stable except blood pressure which client confirmed was her baseline. On site EMS administered 25mg Benadryl IM to right arm, to which client reported feeling slightly better within minutes. On Site EMS contacted on call medical director for further guidance, to which it was recommended that client be evaluated at Hospital ER, client was in agreement for transport. While on site EMS was filling out PCR report client reported new onset symptom of scratchy feeling in throat, EMS administered another 25mg dose of Benadryl at this time. Approximately 6:00 pm client was transported to Hospital ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- client reports taking blood pressure medication in morning, but could not recall the name of the medication (client was vaccinated approximately at 5:10 pm.)
- Allergien
- reports allergy to penicillin.
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Paraesthesia
Symptomtext
Female patient refers an episode of paresthesia in her left upper extremity immediately after receiving the third dose of the Pfizer Vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- V/S WNL O2 SAT: 98, P:85, BP 130/90
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Sleep Apnea, HTN, hypoglycemia, endometriosis
- Andere Medikamente
- Losartan, Vitamin B12
- Allergien
- ASA, SULFA
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood glucose increased
Tremor
Symptomtext
Pfizer booster vaccine administered IM without incident. patient walked to vaccine observation area without incident. Within 15 minutes of have body shaking - in arms and legs. He drank large cup of water. Shaking continued. He states he is diabetic and had just eaten pizza for lunch but had not taken his oral diabetic medication yet. He stated the same shaking happened the last two times he received the covid vaccines - had recevied Moderna for initial series. EMS was present because they were at the clinic for a separate patient., Assessed patient blood sugar 220. BP 180/101. Transported to ER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- diabetic - manages with oral meds
- Andere Medikamente
- metformin, januvia
- Allergien
- unk
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Decreased appetite
Fatigue
Lymphadenopathy
Malaise
Pain
Pyrexia
Rash
Tachycardia
Symptomtext
Fever, chills, body aches, loss of appetite, fatigue, malaise, swollen lymph nodes, rash, tachycardia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Ambien, Remeron, Meltonin
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast pain
Condition aggravated
Discomfort
Immediate post-injection reaction
Injection site discomfort
Injection site pain
Oedema peripheral
Symptomtext
AFTER I GOT THE THIRD DOSE ON JANUARY 5, 2021, I IMMEDIATELY FELT ONLY THE DISCOMFORT OF THE PINCH. THEN THE NEXT DAY I STARTED TO FEEL PAIN IN MY LEFT ARM AND LEFT BREAST, IT WAS PAIN IN BOTH AREAS. ON FRIDAY I CONTINUED WITH THE PAIN, BOTH IN THE ARM AND LEFT BREAST, BUT AN INFLAMMATION UNDER THE LEFT ARM WAS ADDED TO THIS, WHICH CAUSES ME PAIN AND DISCOMFORT AND AN OUT-OF-NORMAL PROTUBERANCE IN MY BODY. IT IS NECESSARY TO ONLY TAKE ACETAMINOPHEN ON THURSDAY AND FRIDAY ONLY ONE DOSE EACH DAY. TODAY SATURDAY, I WOKE UP WITH THE LEFT ARM INFLAMATED, RELATIVELY MY HAND FITS IN THE BULK THAT I HAVE UNDER IT, THE PAIN IN THE LEFT ARM REDUCES, ONLY THE ANNOYANCE REMAINS ON THE SAME, ALSO DISCOMFORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- I HAVE NOT BEEN TO THE DOCTOR YET.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Aspirin
- Vorherige Impfungen
- PAIN IN THE LEFT ARM AND SOMOLENCE
- Staat
- VT
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 07.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Chills
Condition aggravated
Fatigue
Headache
Hyperhidrosis
Insomnia
Myalgia
Pyrexia
Symptomtext
I received my third (booster) dose on Dec 31, 2021 and felt fine for about 12 hours. After that, I awoke with chills and fever around 1AM that prevented me from returning to sleep. By 3AM I experienced muscle aches as well. By 5AM the chills and fever had decreased, but the aches continued and I began to experience severe headaches and mild upset stomach. By 7AM the headaches had decreased to moderate. The headaches fluctuated from moderate to mild by 9AM, and the upset stomach dissipated. I continued to experience moderate muscle aches throughout my body as well as fatigue, headaches, and chills throughout the rest of the day. The second night (Jan 1) was better, I was able to sleep though still experienced continued aches, chills, and sweating. The next day (Jan 2) I had some muscle aches, but no further headaches or chills and I felt ready to resume normal daily functioning. I felt fully recovered by Jan 3.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- history of kidney stones
- Andere Medikamente
- calcium gummy supplement 500mg
- Allergien
- whey protein (milk, cheese, raw eggs)
- Vorherige Impfungen
- Adverse event to previous Covid-19 injection, Pfizer: I received my first dose Jan 22, 2021 (I was age 34) and had no side effec
- Staat
- PR
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hypertension
Symptomtext
Dizziness and High blood pressure 149/110, 159/100, 139/100.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Psoriasis.
- Vorgeschichte
- -
- Andere Medikamente
- None.
- Allergien
- Aspirin; Diflucan.
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Decreased appetite
Dizziness
Dry mouth
Fall
Hyperhidrosis
Mobility decreased
Polyuria
Symptomtext
Within 24 hours of vaccine became excessively weak, fell, couldn't set up in bed, no appetite, light headed, dizzy, dry mouth, excessive urination, sweats. Symptoms chronic for 24 hours, with continuing weakness for several more days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes, high cholesterol, high blood pressure, history of stroke, prostate issue
- Andere Medikamente
- multi-vitamin, Duloxetine, Rosuvastatin Calcium, Asprin EC, Clopidogrel, Lisinopril, Tamsulosin Hcl, Metformin ER
- Allergien
- None
- Vorherige Impfungen
- fatigue following 2nd Phizer covid vaccine
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Injection site hypoaesthesia
Injection site paraesthesia
Paraesthesia
Symptomtext
27yo F patient with no PMH, here for Pfizer COVID vaccine 1st dose. Immediately after receiving the vaccine she was feeling "tingling/numbness" in both the left arm (where the vaccine was inoculated) as well as in her left leg, episode lasted < 1min. Patient is afraid of needles and was also experiencing "Rapid heartbeat" before the vaccine was given. Denies any other symptom. Patient was evaluated by on-site EMS and MD. On PE noted to be AAO x 3; Initial VS: HR 84, RR 20, SpO2 100%, BP 120/70. Heart with RRR, lungs clear bilaterally. After 20min observation patient felt better, repeated set of VS within normal limits. Patient was discharged home with complete resolution of symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Condition aggravated
Dizziness
Fatigue
Headache
Lymphadenopathy
Musculoskeletal stiffness
Myalgia
Pyrexia
Sacral pain
Symptomtext
Fever, Chills, Headache, Lightheaded, Muscle aches, Joint pain, Swollen lymph nodes, Fatigue, Exacerbated POTS symptoms, Sacral pain, Stiff neck. Occurred about 12-18 hours after booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- POTS
- Andere Medikamente
- Metoprolol ER 25mg Once a day, Fludrocortosone .1mg Once a day
- Allergien
- Clindamycin, shellfish allergy
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 25.02.2023
- Impfdatum
- 09.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal discomfort
Exercise tolerance decreased
Fatigue
Influenza like illness
Symptomtext
Gastrointestinal upset, flulike symptoms, frozen hands, long term fatigue and exercise intolerance
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 2 emergency room visits, rheumatology and infectious disease specialist visit, multiple visits to PCP, ongoing counseling
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Fainted after HPV vaccine
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 20.02.2023
- Impfdatum
- 18.02.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 72,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Folliculitis
Pruritus
Symptomtext
About 3 months after having the vaccine administered, I began having intensive itching on my scalp. These symptoms began in May. I also started taking Tremfya in March of 2022. I thought that the itching was due to scalp psoriasis. I contacted my doctor, and she suggested that I treat it with a steroid shampoo called Clobetasol. I used the shampoo every other day, but my symptoms did not improve. I also developed itching on my back. I treated it with over-the-counter Hydrocortisone cream. It helped but did not make it go away. In August I had a n appointment with a dermatologist for my back and he prescribed a stronger steroid cream called Mometasone. This cream did not get rid of the symptoms. In October I saw a new PCP and told her my story. She prescribed Ketoconnozole cream. I also use Ketoconnozole shampoo, and the symptoms got much better over the 2-to-3-month period. I don't believe my symptoms have resolved. I saw a dermatologist in January 2023, and I was diagnosed with having Folliculitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Type 1 Diabetes; Psoriasis; Psoriatic Arthritis; Ventricular Arrythmia
- Andere Medikamente
- Atorvastatin; Valacyclovir; Nadolol; Tremfya; Apidra; Multi-Vitamin; Vitamin C; Vitamin D; Magnesium; Omega 3 Fish Oil
- Allergien
- Shrimp; Crab; Azithromycin; Sulfa Antibiotics; Humira
- Vorherige Impfungen
- Shingles-2019-I felt tired and unwell for a few days.
- Staat
- -
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 08.02.2023
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Rash
Symptomtext
patient says started having skin rash.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none per patient report.
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- mayonnaise, penicillin severity not specified.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 25.01.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 341,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Headache
Symptomtext
I was getting headaches and coughing a lot at first. It got really bad and then I went to the doctor because my coughing was getting so bad. I contacted my doctor and was prescribed prednisone and ROBITUSSIN. I am feeling better now, but still dealing with the cough, it is not as bad though.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Fatigue Immune Deficiency Syndrome; Fibromyalgia; Heart Disease
- Andere Medikamente
- Tirosint; ezetimibe; metoprolol; gabapentin; mirtazapine; ZENPEP; magnesium; vegan EPADHA; vitamin D3; vitamin K; coQ10; methyl B complex; vitamin C complex; NAC; calcium D glucarate; glucosamine chondroitin; glutamine; melatonin; magnesium
- Allergien
- Morphine; codeine; platinum compounds; tape; BENADRYL
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 23.01.2022
- Beginn
- 11.12.2022
- Tage bis Beginn
- 322,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
COVID-19
Electrocardiogram normal
Epistaxis
Mouth haemorrhage
Nasal congestion
Pyrexia
Symptomtext
Got Covid 12/11/2022 fever chills; nose congestion. Developed blood clout in nasal passage; bleeding from mouth and nasal passages. Blood test conducted discovered enema. Prescribed iron supplements.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Blood test conducted discovered enema. ECG also conducted no findings.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Birth control
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 18.01.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 343,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Bronchial wall thickening
COVID-19
Chest X-ray abnormal
Chills
Cough
Fall
Full blood count normal
Gait disturbance
Hypoxia
Influenza like illness
Laboratory test
Limb injury
Lung infiltration
Metabolic function test normal
Musculoskeletal discomfort
SARS-CoV-2 test positive
Symptomtext
Discharge Provider: MD Primary Care Provider : NP Admission Date: 12/27/2022 Discharge Date: 01/07/2023 COVID positive Date: 12/27/2022 Admitting Diagnoses: COVID-19 virus infection PRESENTING PROBLEM: Hypoxia [R09.02] COVID-19 virus infection [U07.1] COVID-19 [U07.1] HOSPITAL COURSE: 84-year-old with medical history of chronic obstructive pulmonary disease on 2-4 L oxygen, recurrent falls, rib fractures, tobacco abuse disorder, hypertension and GERD presenting with flu-like illness that started on 12/26. Patient found to be hypoxic on presentation to ER 12/27, requiring 6 L nasal cannula oxygen. Lab work revealed positive COVID infection. Complete blood count, CMP unremarkable. Chest x-ray showed bilateral basilar bronchial wall thickening and infiltrates concerning for pneumonia. She was admitted to hospitalist service for further management. Patient states that she remembers falling at home and hitting her left shoulder. She was having discomfort in left shoulder and that is what made her come to hospital. She endorsed having cough at baseline, no worsening recently. Denies any recent flu-like illness. Denies any fevers. Endorses chills. No nausea or vomiting. Denies difficulty breathing or chest pain/tightness. Denies lightheadedness. When asked about the fall, she stated getting losing her balance and tripping. Denies any recent change in bowel habits. Patient was treated with IV remdesivir for 5 days and dexamethasone 6 mg daily for 7 days. Patient was able to be weaned down from supplemental oxygen to room air and remained on room air for more than 48 hours. She was evaluated by PT OT and was recommended home health. Patient's daughter states she will not able to take care of the patient at home and requested placement to long-term care. 1/7 patient underwent evaluation for home oxygenation, found to be maintaining her oxygen saturations with room air on both activity and rest. She was discharged in a stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- 11,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pneumonia of left lower lobe due to infectious organism Emphysema of lung Primary hypertension GERD (gastroesophageal reflux disease) Constipation Chronic pain Multiple rib fractures Falls Fracture of right inferior pubic ramus, closed, initial encounter Nondisplaced fracture of right radius Tobacco abuse Rhabdomyolysis Closed fracture of multiple ribs of left side, initial encounter Fracture, humerus Age-related physical debility
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin 81 MG enteric coated tablet hydroCHLOROthiazide (MICROZIDE) 12.5 MG capsule lisinopril (PRINIVIL,ZESTRIL) 2
- Allergien
- Risperidone
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 04.01.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 248,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Malaise
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Generalized malaise; fatigue; mild fever lasted 2-3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid test, positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Blood pressure medication; anti anxiety; PRILOSEC; WELLBUTRIN
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 05.01.2023
- Impfdatum
- 04.01.2022
- Beginn
- 22.12.2022
- Tage bis Beginn
- 352,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Headache
Nasal congestion
Nausea
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
My COVID-19 infection started on 12/22/2022 in the morning around 08:00am. I had a cough, fatigue, runny nose, headache, chest/nasal congestions, nausea, fever of 108.00 while I was in bed. Then I checked my temperature again it was 105.02. I did a home COVID-19 test which was positive. On 12/27/2022 I did a telehealth at my doctor's office with a nurse that prescribe me with Promethazine 4 times a day. I also took over the counter Tylenol every 4 hours and Mucinex D. As of today I still have fatigue, cough, and nasal/chest congestion. On day 9th 01/01/2023 I still tested positive for COVID-19. On day 10th 01/02/2023 I went back to work even though I tested positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 05JAN2023 COVID-19 Test-Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic Back pain; Depression; Anxiety; Fibromyalgia; Malabsorption, B12 Deficiency; History of Gastric Bypass; 2 Cardiac Abrasion
- Andere Medikamente
- Nucynta; Gabapentin; Norco; Synthroid; Aspirin; Vitamin B- Complex; Metoprolol; Partonic; Calcium + D, Vitamin D, B12 Injection; Prozac; Zyrtec
- Allergien
- Anti-Depressants, Levaquin, Adhesive Tape, Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 23.12.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
pain at the injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- none
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 17.11.2022
- Impfdatum
- 29.07.2022
- Beginn
- 30.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Blood test
Symptomtext
The next day I started with joint pain in my wrist and low center back .Within a few days the joint pain was in my arms ,elbows, feet and knees . I seen my family physician several times and treated for the pain. I have been referred to a doctor and he is now treating me for the joint pain. I am on a daily prednisone treatment and I have about 75% improvement as of today with treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- blood levels September and October 18
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- dry mouth syndrome last year
- Andere Medikamente
- zolpidem
- Allergien
- tomatoes,avacado,onions
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 17.02.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 263,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dysarthria
Leukocytosis
Oropharyngeal pain
SARS-CoV-2 test positive
Toxic encephalopathy
Symptomtext
Pt admitted for acute toxic/metabolic encephalopathy and slurred speech. He had leukocytosis and a sore throat and was found to be COVID positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 20.09.2022
- Impfdatum
- 07.02.2022
- Beginn
- 20.09.2022
- Tage bis Beginn
- 225,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
reports that she developed a sore throat and tested positive for covid on home antigen test 9/20/22- has had 1 dose of Janssen and 1 pfizer booster- due now for bivalent booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 17.08.2022
- Impfdatum
- 04.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Biopsy
Blister
Diarrhoea
Dysstasia
Drug ineffective
SARS-CoV-2 test
Suspected COVID-19
Immune system disorder
Influenza virus test
Insulin resistance
Monkeypox
Myalgia
Pyrexia
Swelling
Symptomtext
This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP) from medical information team. The reporter is the patient. A 59-year-old female patient received BNT162b2 (BNT162B2), in 2021 as dose 1, single (Batch/Lot number: unknown), in 2021 as dose 2, single (Batch/Lot number: unknown) and on 04Jan2022 as dose 3 (booster), single (Lot number: FL3209) at the age of 59 years for covid-19 immunisation. The patient's relevant medical history included: "fibromyalgia" (unspecified if ongoing); "diabetes" (unspecified if ongoing); "Raynaud disease" (unspecified if ongoing); "cancer" (unspecified if ongoing); "lupus" (unspecified if ongoing); "allergic to Gluten" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant), outcome "unknown" and all described as "she had all the symptoms of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: negative, notes: she tested negative for COVID-19 with the test kits. Clinical Course: Patient stated that patient had the primary 2-dose series of Pfizer COVID-19 vaccine in 2021 (in (state withheld)). They explained to her that patient might have fever or pain in the injection area up to one day to two days or possibly three days. Stated that patient had lupus, fibromyalgia, diabetes, Raynaud disease, and cancer, patient had been on the cancer medication for 4 years with which she only had nausea and headache, patient asked her doctor if she could take it at night, and patient did so, to avoid those symptoms during the day and be an active person. Pfizer had supplied to her the medication AROMASIN Exemestane 25 mg tablets, for 4 years, and patient had an appointment scheduled for Oct at local Cancer Center. Patient had all the symptoms of COVID-19, but patient tested negative for COVID-19 with the test kits that patient purchased at the (pharmacy name withheld) inside (state name withheld)). Patient was diabetic and had been taking her medications and injecting insulin, without issues, until the day after patient received the booster dose of Pfizer COVID-19 vaccine (in (place name withheld)) lot number FL3209 on 04Jan2022. Since then, patient stated that patient fell in bed, and patient still has symptoms to this day 11Aug2022, the booster messed up her life, it is still the same, it harmed her system and patient wonders if the vaccine altered her immune system. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Negative; Comments: she tested negative for COVID-19 with the test kits.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Cancer; Diabetes; Fibromyalgia; Gluten sensitivity; Lupus erythematosus; Raynaud's disease
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 28.07.2022
- Beginn
- 07.08.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Nausea
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sinonasal obstruction
Symptomtext
I did not have an adverse reaction to the vaccine. I tested positive for COVID-19 on 08/07/2022 with a home test. My symptoms where nasal blockage; coughing really bad; nauseated and a sore throat. I contacted my doctor on 08/10/2022 and due to my current medication I was advised not to take Plaxovid so they said to take Tylenol, Mucinex and throat lozenges. As of today I still have congestion, runny nose and cough. The cough is not as bad but I still have it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- Home test COVID-19 positive 08/07/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Thyroid condition
- Andere Medikamente
- Metformin; Omeprazole; Atorvastatin; Latornine; B12 injection; Amlodipine; Spironolactone; Carvedilol; Vita One-Day; Viatin; Melatonin
- Allergien
- Penicillin; Cipro; Septra; Sulfa drugs; Pneumonia vaccine 23
- Vorherige Impfungen
- Pneumonia vaccine I had a swollen arm.
- Staat
- FL
- Alter
- -
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 04.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Congenital musculoskeletal disorder of spine
Diarrhoea
Fall
Pyrexia
Symptomtext
had surgery on his spine, he has screws and cannot bend; diarrhea; fever; she stated that she fell in bed along with her brother; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. A male patient received BNT162b2 (BNT162B2), on 04Jan2022 as dose 3 (booster), single (Lot number: FL3209) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete, Unknown Manufacturer), for COVID-19 Immunization. The following information was reported: CONGENITAL MUSCULOSKELETAL DISORDER OF SPINE (medically significant), outcome "unknown", described as "had surgery on his spine, he has screws and cannot bend"; DIARRHOEA (non-serious), outcome "unknown", described as "diarrhea"; PYREXIA (non-serious), outcome "unknown", described as "fever"; FALL (non-serious), outcome "unknown", described as "she stated that she fell in bed along with her brother". Therapeutic measures were taken as a result of congenital musculoskeletal disorder of spine. Clinical course: The patient received the same booster dose as was given to reporter, on the same day in the same place, the same injection from the same nurse. Since patient was vaccinated, patient fell in bed. The patient was in bed for 4 days, woke up to go to the bathroom because patient had diarrhea, and had fever. The patient got up and continued to do his daily life, with his back condition, but he was able to get up. The patient had surgery on his spine, he was merged from L1 to sacral S1, S2, S3, S4, he has screws and cannot bend, and does not like to take medicines so the doctor gave him the option to use medical cannabis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 28.07.2022
- Impfdatum
- 22.01.2022
- Beginn
- 04.07.2022
- Tage bis Beginn
- 163,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
COVID-19
Cough
Fatigue
Feeling abnormal
Feeling cold
Influenza virus test negative
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I firmly believe that I was exposed while at physical therapy because I had noticed that they do not properly clean their machines between use. I attended physical therapy 06/30/2022, then on the morning of 07/04/2022, I woke up at 3AM with a sore throat and was very cold. I got up at 6AM to care for a relative. I was still feeling badly though, so I went to an urgent care clinic. My temperature was 102.1. They tested for flu and COVID-19. I was positive for COVID-19 and they prescribed PAXLOVID. I began my first dose that morning. My fever ended up reaching 104 but by Tuesday, I was only experiencing a sore throat and some coughing. I did lose my taste and smell at some point. By the third day, I felt much better and was just experiencing some fatigue and coughing. After taking the 5 days of PAXLOVID, I tested negative for COVID-19 on the 6th day. It has been weeks since I have tested negative for COVID-19 but I am still coughing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Flu test negative; COVID-19 test positive 07/04/2022.
- Aktuelle Erkrankungen
- Ear and sinus infection.
- Vorgeschichte
- None
- Andere Medikamente
- Duloxetine; DULERA inhaler; vitamin C; zinc.
- Allergien
- BIAXIN; bananas; dissolvable sutures.
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 152,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
COVID-19
Fatigue
Neck pain
Pain
SARS-CoV-2 test positive
Throat irritation
Vaccine breakthrough infection
Symptomtext
Breakthrough case of COVID-19; I had two to three days of neck pain followed by back and knee pain. Wherever I have metal in my body hurt very bad. I then had a scratchy throat 48 hours before I took the test, then for the next 4 days after being tested positive, I had extreme body aches and extreme fatigue. I have basically recovered but just am still extremely tired and fatigue. I did take the PAXLOVID as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- COVID-19 PCR test positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Losartan; DSS; CELEBREX; triamterene; amlodipine; estradiol norethindrone; CITRACAL; vitamin C; vitamin B complex
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 16.04.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 87,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I started getting symptoms of a sore throat and headache for 3-4 days then went away. I took an at home COVID-19 test that was positive. I contacted my doctor with a telehealth visit and was prescribed Paxlovid. After the Paxlovid, my symptoms went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 test - positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN
- Andere Medikamente
- Atorvastatin; Omeprazole; Nebivolol; Ramipril; Aspirin; Zolpidem
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 02.07.2022
- Tage bis Beginn
- 81,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Oropharyngeal pain
Pain
Respiratory tract congestion
SARS-CoV-2 test
Symptomtext
I was traveling, consulted with my doctor before hand because I am diabetic and about 65 and he gave me the green light. I know the COVID-19 cases is very low where I was traveling to, I never had any symptoms during the week I was there. I then flew to first layover, and visited my son and ate at a restaurant. Then flew to the nest lay over the next day, and developed symptoms about two days later, 07/02. First couple of days were the worst. It wasn't terrible, temperature of 100.2, very congested, sore throat, and some additional symptoms later on of headache, achiness. I never get headaches so that one was very unusual for me. I contacted my Doctor via email and he prescribed Paxlovid for me on July 5th, which was already 3 days in of symptoms. I spread it to my wife, her case was definitely more severe, and I think my dog contracted it as well, and a few friends I had contact. My symptoms went away after about 5 days and then came back about two days with the sore throat and bad congestion. Im still struggling with some of the symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- at home COVID-19 test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes; High Cholesterol; Prostate Cancer (August 2014)
- Andere Medikamente
- Metformin; Bupropion; Jardiance; Lisinopril; Januvia; Simvastatin; Low dose Aspirin; Montelukast as needed
- Allergien
- Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 120,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site indentation
Injection site scab
Symptomtext
Client called stating that she had her booster COVID-19 vaccination in January 2022. Four months later, a "dent at the injection site" and a scab appeared at the injection site. Client states she had a physical, but this complaint was not addressed at the visit. The client has not sought medial care for this complaint. While taking her to the pediatrician, the pediatrician asked what happened to the clients arm. She stated it was from her COVID-19 vaccine. Dr. advised to have it assessed. Client called the Health Department. The client was asked to relay the events and her concerns. Client was advised to see a healthcare provider about this complaint as soon as possible. Client was given information about VAERS and that a report would be submitted by Health Staff.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site indentation
- Hospital-Tage
- -
- Labordaten
- None at this time.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 05.04.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 73,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Back injury
Back pain
COVID-19
Fall
Lower respiratory tract infection
Productive cough
SARS-CoV-2 test positive
Symptomtext
On 06/17/2022, we had taken a trip and I was coughing up a lot of mucus, I fell in the tub and I hurt my back. I was still having pain, so on 06/22/2022, I went to urgent care for my back. I mentioned my chest cold, they tested me for COVID-19 and the test came back positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 test on 06/22/2022 - positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetic
- Andere Medikamente
- LIPITOR; lisinopril; atenolol; finasteride; PLAVIX; aloe vera extract; linolenic acid; omega 3 fish oil
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 70,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Malaise
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Contracted Covid, moderate symptoms, including sore throat, coughing, congestion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- PCR test on 6/17/22 confirmed Covid
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin d
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 83,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Cough
Dysphagia
Fatigue
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
On 4/6/2022, I received my second Pfizer booster for COVID-19. On 6/28/2022, I began almost constantly coughing and had sore throat with throat congestion and extreme fatigue. On 6/29/2022, I took an at-home test for COVID-19, and the result was positive. I called my doctor's office. They asked me if I wanted an antiviral, and I let them prescribe me Paxlovid. However, I only took a couple of the Paxlovid, as they are huge pills, and I'm afraid of choking. I contacted my doctor to let her know, and I was prescribed molnupiravir in place of the Paxlovid, I took a couple of the molnupiravir capsules, but I also had difficulty swallowing those. I informed my doctor of this, and she was fine with my discontinuing the medication. I saw my doctor on 7/5/2022 for an annual exam. I actually felt well that day, but 7/6/2022, I was extremely fatigued. Since 7/4/2022, the coughing has greatly diminished. At the time of this writing, the sore throat and congestion are gone. The only lingering symptom is the fatigue, and I have good and bad days. There are days in which I feel fine and have my normal level of energy, but then are also days in which I am wiped out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Graves Disease; Osteoporosis.
- Andere Medikamente
- Levothyroxine; Alendronate; Vitamin D.
- Allergien
- Oxycodone.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 29.06.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Neck pain
Pain in extremity
Symptomtext
Patient stated that her arm was sore to her elbow and up to her neck after she had the vaccine. It lasted for about 3-4 weeks. Patient didn't seek any medical treatment and it resolved on its own
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- muscle spasms
- Vorgeschichte
- muscle spasms
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 28.06.2022
- Impfdatum
- 11.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- - / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Biopsy kidney abnormal
Blood cholesterol increased
Blood creatinine increased
Decreased appetite
Fatigue
Glycosuria
Inappropriate schedule of product administration
Pain in extremity
Protein urine
Pyrexia
Renal impairment
Tubulointerstitial nephritis
Symptomtext
Patient had a sore arm after both doses (Pfizer dose #1 1/18/22 and Pfizer dose#2 2/11/22) but after second dose developed fatigue 5 days later and then had fevers staring 2/24/22 (T 103 F), poor appetite and was admitted to the hospital Presented with fever and elevated creatinine Dx: Interstitial nephritis confirmed by biopsy. Treatment with steroids. Pulse methylprednisolone for 3 days, daily prednisone 1mg/kg for 2 weeks, and then spaced to every other day for a week with worsened kidney function. Restarted steroids 1mg/kg for 4 weeks and then completing a steroid taper of 10 mg every week that then decreased to 5 mg for a week to end the taper.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- 13,0
- Labordaten
- 2/28/22 creatinine 1.59;3/4/22 glucosuria 50 g/dl 3/12/22 glucosuria > 500 mg/dl Additional information for Item 19: 3/10/22 creatinine 3.26 5/27/22- cholesterol 310, creatinine 0.78, urine protein/creatinine 0.147
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- multivitamin and occasional melatonin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- M
- Eingang
- 16.06.2022
- Impfdatum
- 07.01.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 115,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Vaccination failure
Neck pain
Pain in extremity
Symptomtext
Each of us had a Covid infection with light to no symptoms; Each of us had a Covid infection with light to no symptoms; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52-year-old male patient received BNT162b2 (BNT162B2), on 13Mar2021 at 15:00 as dose 1, single (Lot number: En6199), in left arm, on 03Apr2021 at 14:00 as dose 2, single (Lot number: Er8734), in left arm and on 07Jan2022 at 16:00 as dose 3 (booster), single (Lot number: Fl3209), in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: NASONEX; SUDAFED [XYLOMETAZOLINE HYDROCHLORIDE]. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 02May2022 at 15:00, outcome "unknown" and all described as "Each of us had a Covid infection with light to no symptoms". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (31Jan2022) Positive, notes: Nasal Swab. Clinical Course: Severe Pain in left neck and left arm. 3 male employees at a office of 24 are experiencing the same symptoms. The only thing we all have in common is the Pfizer shots. We are of different ethnicity's and age. We each have a past neck diagnosis issue from over 10 years ago. . None of him have had any issues with they necks or arms up to this year from Previous issue. Seems like to much of a coincidence that its' not either a side effect of the vaccine or a side effect of Covid. Each of him had a Covid infection with light to no symptoms. The symptoms are ongoing with health care being administered with PT.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200824355 same product/event, different patient;US-PFIZER INC-202200828047 same reporter/patient, different dose/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220131; Test Name: Bionax; Test Result: Positive ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- NASONEX; SUDAFED [XYLOMETAZOLINE HYDROCHLORIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 07.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Neck pain
Vaccination site pain
Symptomtext
Severe Pain in left neck and left arm; Severe Pain in left neck and left arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A male patient received BNT162b2 (BNT162B2), on 07Jan2022 at 16:00 as dose 3 (booster), single (Lot number: Fl3209), in left arm for covid-19 immunisation. The patient's relevant medical history included: "neck diagnosis issue", notes: from over 10 years ago. Concomitant medication(s) included: NASONEX; SUDAFED [PSEUDOEPHEDRINE HYDROCHLORIDE]. Vaccination history included: BNT162b2 (DOSE 1, LOT NO: En6199, LOCATION: Left arm), administration date: 13Mar2021, for COVID-19 immunization; BNT162b2 (DOSE 2, LOT NO: Er8734, LOCATION: Left arm), administration date: 03Apr2021, for COVID-19 immunization. The following information was reported: NECK PAIN (non-serious), VACCINATION SITE PAIN (non-serious), outcome "unknown" and all described as "Severe Pain in left neck and left arm". Therapeutic measures were taken as a result of neck pain, vaccination site pain. Additional information: The patient have no known allergies. Patient have no other vaccine in four weeks. Patient have no COVID prior to vaccination. None of us have had any issues with our necks or arms up to this year from previous issue. Seems like to much of a coincidence that it's not either a side effect of the vaccine or a side effect of COVID. Sender's Comments: Linked Report(s) : US-PFIZER INC-202200828045 same reporter/product/event, different patient; US-PFIZER INC-202200828043 same reporter/product/event, different patient; US-PFIZER INC-202200828046 same reporter/patient, different dose/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Ill-defined disorder (from over 10 years ago.)
- Andere Medikamente
- NASONEX; SUDAFED [PSEUDOEPHEDRINE HYDROCHLORIDE.]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 07.01.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 115,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Neck pain
Pain in extremity
SARS-CoV-2 test
Symptomtext
Severe Pain in left neck and left arm; Severe Pain in left neck and left arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A male patient received BNT162b2 (BNT162B2), on 07Jan2022 at 16:00 as dose 3 (booster), single (Lot number: Fl3209), in left arm for covid-19 immunisation. The patient's relevant medical history included: "neck diagnosis issue" (unspecified if ongoing). Concomitant medication(s) included: NASONEX; SUDAFED 12 HOUR. Vaccination history included: BNT162b2 (Dose 1, Prev dose product: COVID 19, Prev dose brand: Pfizer BioNTech, Prev dose lot number: En6199, Prev dose administration time=03:00 PM, Prev dose vaccine location=Left arm), administration date: 13Mar2021, for Covid-19 immunization; BNT162b2 (Dose 2, Prev dose product: COVID 19, Prev dose brand: Pfizer biontech, Prev dose lot number: Er8734, Prev dose administration time=02:00 PM, Prev dose vaccine location=Left arm), administration date: 03Apr2021, for COVID-19 immunization. The following information was reported: NECK PAIN (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 02May2022 at 15:00, outcome "not recovered" and all described as "Severe Pain in left neck and left arm". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of neck pain, pain in extremity. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200828047 same reporter/product/event, different patient;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220131; Test Name: Bionax Test; Test Result: Positive ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Neck discomfort
- Andere Medikamente
- NASONEX; SUDAFED 12 HOUR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Headache
Immediate post-injection reaction
Joint range of motion decreased
Neck pain
Pain in extremity
Symptomtext
Started w/pain in the arm (left) immediately after the shot. Progressed to neck and Headache. Patient has had pain in the arm that the vaccine was given on for 4 month now. Patient takes tylenol & tramadol for pain. The pain causes a lot of discomfort and also decreased Range of motion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyperlipidemia, Gout, Hypertension, Rheumatoid Arthritis, DM Type 2, Herpes Simplex, Obesity.
- Andere Medikamente
- ferrous sulfate; furosemide; True Metrix Glucose Meter; Actos; Tylenol; glucosam-chond-msm; Trueplus Lancets; allopurinol; potassium chloride; Humira(CF) Pen; tramadol; methotrexate sodium; rosuvastatin; metformin; Miralax; losartan; aspiri
- Allergien
- Januvia, Listerine Mouthwash
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 04.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test negative
Angioedema
Antinuclear antibody positive
Arthralgia
Biopsy skin abnormal
C-reactive protein increased
Contusion
Henoch-Schonlein purpura
Inflammation
Red blood cell sedimentation rate increased
Tinnitus
Urticaria
Symptomtext
Several days after my Covid booster, I developed a case of chronic, raging hives (and angiodema) that has continued for 6 months (and counting). It has gotten progressively worse over time, and has not responded well to antihistimes (even at 4x regular dosing, per my allergist) and has not responded to Xolair. I also have developed a case of HSP/IgA vasculitis since my booster (confirmed by biopsy). I had this condition as a child, and I believe my booster may have caused it to be reactivated for the first time ever. I've had widespread bruising over my legs, torso, and arms, along with the hives. The bruising started about a month ago. I've also had joint pain and ringing in my ears ever since my booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- - Allergy testing was conducted in February 2022 and ruled out allergies. - Autoimmune disease such as lupus and sjogren's were ruled out (at least for now) (February 2022) - ANA labs are positive and continue to increase each time tested. (February 2022, May 2022) - CRP and ESR markers for inflammation elevated (May 2022) - biopsy confirming HSP/IgA vasculitis May 2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Celiac disease; Hashimotos thyroiditis
- Andere Medikamente
- NP Thyroid
- Allergien
- Gluten
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 22.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Apathy
Depression
Loss of personal independence in daily activities
Vaccination site injury
Vaccination site pruritus
Symptomtext
Severe depression; I had anxiety and depression for most of my life; this is the depression like I never experienced before; My depression has daily getting significantly worse over the past years; Lack of motivation; I spend rest of my time at bed just because I have no motivation to get up and do anything.; got to a point where I could no longer function and wasn't able to like to get out the bed to work; Itchy Vaccine Injury; Vaccine site injury; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 40-year-old female patient received BNT162b2 (BNT162B2), on 17Apr2021 as dose 1 , single (Lot number: ER8731), on 08May2021 as dose 2 , single (Lot number: ER8736) and on 22Jan2022 as dose 3 (booster), single (Lot number: FL3209) at the age of 40 years for covid-19 immunisation. The patient's relevant medical history included: "Fibromyalgia" (unspecified if ongoing), notes: Pregabalin 150 mg capsule, one capsule twice a day. Taking Cyclobenzaprine 10 mg tablet at bed time; "Chronic headaches" (unspecified if ongoing), notes: Chronic headaches; "Migraine" (ongoing), notes: Migraine; "Asthma" (ongoing), notes: Asthma, Taking Montelukast. Taking 10 mg tablet once a day.; "GERD" (ongoing), notes: GERD, Taking Pantoprazole 40 mg tablet twice a day.; "Depression" (ongoing), notes: depression has daily getting significantly worse over the past years; "anxiety" (ongoing), notes: I had anxiety and depression for most of my life.; "difficulty concentrating." (unspecified if ongoing), notes: I also have difficulty concentrating.; "Lack of motivation" (unspecified if ongoing), notes: I spend rest of my time at bed just because I have no motivation to get up and do anything. Concomitant medication(s) included: TRINTELLIX taken for depression; ALPRAZOLAM ER; FLUVOXAMINE, start date: 23Mar2022; VENLAFAXINE XR; TOPIRAMATE taken for migraine; MONTELUKAST taken for asthma; CETRIZINE taken for hypersensitivity; PREGABALIN taken for fibromyalgia; CYCLOBENZAPRINE taken for fibromyalgia; PANTOPRAZOLE taken for gastrooesophageal reflux disease. The following information was reported: DEPRESSION (disability, medically significant), outcome "unknown", described as "Severe depression; I had anxiety and depression for most of my life; this is the depression like I never experienced before; My depression has daily getting significantly worse over the past years"; APATHY (non-serious), outcome "unknown", described as "Lack of motivation; I spend rest of my time at bed just because I have no motivation to get up and do anything."; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious), outcome "unknown", described as "got to a point where I could no longer function and wasn't able to like to get out the bed to work"; VACCINATION SITE PRURITUS (non-serious), outcome "unknown", described as "Itchy Vaccine Injury"; VACCINATION SITE INJURY (non-serious), outcome "unknown", described as "Vaccine site injury". Therapeutic measures were taken as a result of depression, apathy. Clinical course: Pfizer Employee stated, "patient have been experiencing severe depression. patient also have difficulty concentrating, lack of motivation and when patient saw Psychiatrist earlier that week she said she believe it the itchy vaccine injury from the COVID Vaccine. Yes, that she told me." When paraphrased the concern, Pfizer employee stated, "Yes, patient had anxiety and depression for most of my life but this is the depression like never experienced before." Pfizer employee stated, "It's hard to pin point a specific date. patient depression has been getting significantly worse over the past years (Further clarifications unknown). patient got to a point where could no longer function and wasn't able to like to get out the bed to work. patient would say this month, would say more got bad just bad but it is getting significantly worse over the past year. When medication for depression and anxiety, Pfizer employee stated, "A lot of medication for that. I am on, I before my, before my depression I was still taking Trintellix 20 mg, yes it is for depression. I am currently taking it but the dosage was changed so I was previously taking it at 20 mg, once a day and then I can tell you when it was changed, on 26Apr2022 my psychiatrist changes it to 10 mg, once a day. Currently, I am taking 10mg. I take Alprazolam, extended release, that's the 1 mg tablet. I take that twice a day. Before that it was 20. Currently I am only taking once a day. She put me on something, she added something else and then she decrease the Trintellix. I haven't told you about that, so the new medicine that she gave me is called Fluvoxamine, so on 23Mar, I started taking at 50 mg once a day on 23Mar2022 and then on April 26Apr, when she decreases my Trintellix, she doubled the dosage of Fluvoxamine to 50 mg twice a day and then when I saw her on Tuesday 24May, she increase the Fluvoxamine again to taking a 100 mg in the morning and 50 mg at night. Yeah, that started on the 24th. I also had Alprazolam, that is immediate release, it is 0.5 mg it's a tablet and I just as needed for break through anxiety. Yes, that's the immediate release as I take it as needed as 25 mg (Not clarified) and then I have the extended release as I told you about earlier but I take 0.5. Venlafaxine Extended Release. If you want I can give you information, I take a lot of medication, Topiramate Extended Release (Captured as provided) 100mg, 100 mg capsule, one capsule for twice daily and that's for my chronic migraine." Pfizer employee stated, "Yes, I am on out on medically 'leave' usually dealing short time disability (Further clarification unknown hence event captured as per verbatim). I have right now. No, Not so much feeling anxiety is more, it's the depression that's causing the problem. I have some good day mostly bad days. I spend rest of my time in bed just because I have no motivation to get up and do anything." When probed for the treatment, Pfizer employee stated, "Not other than what I early told you that my Psychiatrist start reaching my medication around. She told me when I saw her on Tuesday that she is expecting or she has heard that there should be release of information regarding how she she treat those with vaccine injuries and long COVID and she was waiting to see what that recommendation is before she tell me to any further coarse of treatment." No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Anxiety (I had anxiety and depression for most of my life.); Asthma (Asthma Taking Montelukast. Taking 10 mg tablet once a day.); Depression (depression has daily getting significantly worse over the past years); GERD (GERD Taking Pantoprazole 40 mg tablet twice a day.); Migraine (Migraine)
- Vorgeschichte
- Medical History/Concurrent Conditions: Chronic headaches; Concentration impairment (I also have difficulty concentrating.); Fibromyalgia; Lack of motivation (I spend rest of my time at bed just because I have no motivation to get up and do anything.)
- Andere Medikamente
- TRINTELLIX; ALPRAZOLAM ER; FLUVOXAMINE; VENLAFAXINE XR; TOPIRAMATE; MONTELUKAST; CETRIZINE; PREGABALIN; CYCLOBENZAPRINE; PANTOPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 06.01.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 123,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Ear infection
Nasal congestion
Oropharyngeal pain
Productive cough
Pyrexia
Respiratory disorder
SARS-CoV-2 test
Symptomtext
respiratory; sore throat; ear infection; congestion; cough; cough progressively worsened and became productive; low grade fever; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). The reporter is the patient. A 15-year-old male patient received BNT162b2 (BNT162B2), on 06Jan2022 as dose 3 (booster), single (Lot number: FL3209) at the age of 15 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: DOXYCYCLINE taken for acne. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Site of injection: L. arm (Left Arm), Covid-19 Vaccine name: Pfizer, Batch/Lot number: EW0167), administration date: 17May2021, when the patient was 14-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 2, SINGLE, Site of injection: L. arm (Left Arm), Covid-19 Vaccine name: Pfizer, Batch/Lot number: EW0191), administration date: 09Jun2021, when the patient was 14-year-old, for COVID-19 Immunization. The following information was reported: COUGH (non-serious) with onset 09May2022, outcome "unknown"; PRODUCTIVE COUGH (non-serious) with onset 09May2022, outcome "unknown", described as "cough progressively worsened and became productive"; PYREXIA (non-serious) with onset 09May2022, outcome "unknown", described as "low grade fever"; NASAL CONGESTION (non-serious) with onset 18May2022, outcome "unknown", described as "congestion"; EAR INFECTION (non-serious) with onset 20May2022, outcome "unknown"; RESPIRATORY DISORDER (non-serious), outcome "unknown", described as "respiratory"; OROPHARYNGEAL PAIN (non-serious), outcome "unknown", described as "sore throat". Relevant laboratory tests and procedures are available in the appropriate section. Additional Information: It was unknown whether patient have Sars-CoV2 antibodies at diagnosis. The patient was not hospitalized. The patient was not admitted to an intensive care unit. The patient did not display clinical signs at rest indicative of severe systemic illness. Patient had cough and sore throat during initial 10 days. Cough progressively worsened and became productive week of 09May2022. One day of low grade fever. Congestion began 18May2022 and ear infection documented 20May2022. Patient's outcome with Covid-19 was recovering. It was unknown from how many days from SARS-CoV2 diagnosis did it take before the SARS-CoV2 antigen test became negative. The patient was not a smoker/former smoker. The patient was taking other medication routinely prior to the event being reported which included: MVI, Doxycycline 50 mg 2 tab QD for acne. The patient did not have any pre-existing disease worsened during the SARS-CoV2 infection. The patient had not been treated with immunomodulating or immunosuppressing medication or received any other vaccines around the time of covid-19 vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220428; Test Name: rapid antigen at home test; Test Result: Positive; Comments: Pt (Patient) had a positive rapid antigen at home test on 28Apr2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- DOXYCYCLINE.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Urticaria
Symptomtext
Urticaria beginning 20 minutes after receiving the vaccine until now which is 2 weeks post-vaccination. She was seen in the ER and given prednisone, Pepcid and diphenhydramine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Ataxia
Headache
Hyperhidrosis
Oropharyngeal pain
Pain in extremity
Pyrexia
Sensitive skin
Symptomtext
5/26/22 10;00 PM FEVER T103, SWEATS 5/27/22 RIGHT ARM PAIN, ACHING EVERYWHERE JOINTS, SKIN SENSITIVITY, H/A, SORE THROAT, MILD ATAXIA X 3 DAYS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- NONE HE DID NOT GET TESTED
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 24.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
Injection site pain
Injection site swelling
Joint range of motion decreased
Symptomtext
shoulder joint pain and limited range of motion swelling and soreness around the injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 06.04.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Headache
Injection site pain
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sinus disorder
Vaccine breakthrough infection
Symptomtext
I started having symptoms of sinus issues with headache, runny nose, fatigue on 5-10-2022. On 5-11, I started running fever up to 100.0 with body aches. I took a home test for Covid on 5-12 and it was positive. I called the doctor on the same day and asked her for treatment. She called in Paxlovid and I took it for 5 days. Then I took another home test on 5-17 and it was negative. I have since taken two more home tests with one faint positive and the second showed negative. I did experience extreme fatigue and soreness at injection site after dose 4 Pfizer. I am reporting my breakthrough case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home Covid tests on 5-12, 5-17, 5-18, 5-19.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Arthritis
- Andere Medikamente
- Celebrex 200mg daily; lisinopril 2 tabs daily; levothyroxine daily; baby aspirin daily; calcium daily; multivitamin daily; Zyrtec daily
- Allergien
- None; seasonal allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 11.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site induration
Injection site pain
Similar reaction on previous exposure to drug
Symptomtext
Both arms red and tender localized at injection site. Left arm with mild induration at injection site. Per patient redness and tenderness were resolving compared to site condition the first two days post vaccination. No concerns of skin infection at this time; per patient local and similar reactions happened before with other vaccines including prior doses of Pfizer covid19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- pre diabetes per patient
- Vorgeschichte
- allergic rhinitis
- Andere Medikamente
- famotidine sucralfate voltaren acetaminophen
- Allergien
- NKA
- Vorherige Impfungen
- Pfizer COVID19, influenza, varicella
- Staat
- -
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 06.03.2021
- Beginn
- 11.02.2022
- Tage bis Beginn
- 342,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
COVID-19
Nausea
SARS-CoV-2 test positive
Vomiting
Symptomtext
02/11/22 presents to ED for "Abdominal Pain, Nausea And Vomiting". PMHx of "GERD, abdominal pain, elevated blood pressure, vitamin D deficiency, postgastrectomy malabsorption, status post conversion of gastric sleeve for gastric bypass and hiatal hernia repair 11/21, history of appendectomy, history of cholecystectomy, history of hysterectomy"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- 02/12/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 13.01.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 77,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Activated partial thromboplastin time shortened
Alanine aminotransferase increased
Aspartate aminotransferase increased
Biopsy liver abnormal
Blood alkaline phosphatase increased
Blood bilirubin increased
Blood glucose normal
Blood immunoglobulin A
Blood immunoglobulin A increased
Blood iron increased
Blood thyroid stimulating hormone
Computerised tomogram abdomen normal
Full blood count
Gamma-glutamyltransferase
Globulins increased
Haematocrit decreased
Haemochromatosis
Symptomtext
Significantly elevated hepatic functions, nausea and vomiting and abdominal pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- 3/31/22 - CMP (glucose 116, protein 9.6, globulin 5.8, bilirubin 2.6, alk phos 132, AST 908, ALT 954). CBC (leukocytes 4.1, Erythrocytes 3.69, hemoglobin 11.4, hematocrit 33.9, erythrocyte distribution width SD 52.5, erythrocytes distribution width CV 15.8, monocytes 15, neutrophils absolute 1.73 4/1/22 - lipase and hepatitis acute panel normal 4/5/22 - CBC, CMP abnormal like above 4/7/22 - PTT 35, INR 1.5, NASH fibrosure unable to calculate, celiac panel showed elevated IgA at 416, smooth muscle 85, iron 246, IGG 4841, ferritin 312, GGT 112, acetaminophen , TSH, hemochromatosis, seruloplasmin, AMA, and A1A normal, 4/1/22 CT abd/pelvis normal 4/6/22 US abd nonspecific findings that could be associated with hepatitis 4/11/22 Liver biopsy positive for autoimmune hepatitis
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Scoliosis, Chiari I malformation, migraine, obesity
- Andere Medikamente
- Omeprazole, Rizatriptan PRN, acetaminophen PRN, melatonin PRN
- Allergien
- Amoxicillin, adhesive tape
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 14.04.2022
- Beginn
- 30.04.2022
- Tage bis Beginn
- 16,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Cough
Disorientation
Fatigue
Malaise
Rhinorrhoea
SARS-CoV-2 test positive
Somnolence
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID-19 Case: I received my 2nd booster on April 14th. I had no immediate symptoms. I first started noticing symptoms on Saturday, April 30th. runny nose and cough. On Monday morning, I saw a doctor and she recommended Flonase and Zyrtec, on Tuesday morning, it tested positive for COVID-19. She prescribed Paxlovid in addition to Mucinex DM, Zyrtec. I feel weak, disoriented, fatigued and sleepy. I assume it has to do with the Mucinex DM, Flonase, and runny nose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Rapid Antigen Test - Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Cholesterol and Blood Pressure
- Andere Medikamente
- Daily - Atorvastatin 80mg Olmesartan-HCTZ 40-12.5mg Men's Complete Multivitamin One a Day Sunday, Monday, Wed, and Fri: 81mg Aspirin Tuesday, Thursday, and Saturdays: Magnesium, Zinc, Vitamin E, Coconut Oil
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Vaccination site pain
Symptomtext
Left arm pain injestion location after still 4 months and numbness in arm and hand.; Left arm pain injestion location after still 4 months and numbness in arm and hand.; Left arm pain injestion location after still 4 months and numbness in arm and hand.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Jan2022 at 09:15 as dose 3 (booster), single (Lot number: FL3209) at the age of 59 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Past drug history included: Codine, reaction(s): "known allergies: Codine", notes: known allergies: Codine. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: ER8727, Location of injection: Arm Left, Vaccine Administration Time: 07:30 AM), administration date: 25Mar2021, when the patient was 58-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EN6202, Location of injection: Arm Left, Vaccine Administration Time: 07:30 AM), administration date: 04Mar2021, when the patient was 58-year-old, for COVID-19 immunization. The following information was reported: VACCINATION SITE PAIN (non-serious), HYPOAESTHESIA (non-serious), HYPOAESTHESIA (non-serious) all with onset 28Jan2022 at 10:00, outcome "not recovered" and all described as "Left arm pain injestion location after still 4 months and numbness in arm and hand.". Therapeutic measures were not taken as a result of vaccination site pain, hypoaesthesia, hypoaesthesia. Additional Information: The patient received no other vaccines within 4 weeks prior to the COVID vaccine. Any other medications the patient received within 2 weeks of vaccination was Multi-vitamin. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19 No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test abnormal
Chills
Herpes simplex test positive
Pain
Pyrexia
Rash
Sciatica
Symptomtext
After receiving vaccine on 02/5/2021, I had a rash on back on left thigh felt like a sciatica pain along with fever chills. 6 days later after booster on 12/7/2022 I had the same reaction with the rash on the back on leg and severe pain and chills. I treat it with Valtrex and after about 11 days it went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Blood test to confirm it was herpes 2.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D Supplement; Estradiol Patch; Benadryl; Tylenol; Tretinoin
- Allergien
- Penicillin; Gluten; Dairy; Oats; Almonds; Raw Carrots; Barley; Hazelnuts; Eggs; Sulfa; Erythromycin; Propofol
- Vorherige Impfungen
- All COVID-19 vaccine
- Staat
- OR
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 20.01.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Furuncle
Rash
Rash erythematous
Rash papular
Rash pruritic
Swelling
Urticaria
Symptomtext
I had these welts on the back of my head that were raised but flat and about the size of a quarter. I kept an eye on it for about a week or two then they went away. On 03/15/2022 in the evening I felt a small raised spot on the crown of my head that itched. I went and looks in the mirror and it was a small red dot and I scratched it. That evening I noticed the spot had gotten bigger and it hurt. It also started to spread all the way down the back of my neck and spread toward the sides. They don't have a white heads. Each one is about the size of a dime in diameter. I have tried topical ointments that have not helped. I also used Chlorhexidine gluconate which also did not help. I did go to the doctor and they did a scrape test and they couldn't find a cause. She did say that they boils were puss filled. A tea tree shampoo and condition did seem to help with the itching. I also ground up aspirin and mixed it with coconut oil to use topically and it definitely seems to help. Now the itching is on the top of my head and the back of my neck. It is about 95% better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic Fatigue Syndrome Fibromyalgia Ehlrs Danlos Syndrome Type IIII- Vascular
- Andere Medikamente
- CBD 50mg at night, Benadryl, Citrus Bergamot, Vitamin B, Vitamin D, Vitamin K, Levothyroxine 88mcg once daily, 1.5mg Estrogen and 10mg Testosterones bio identical, Disodium phosphate Bladderwrack, Strattera 80mg once daily, 100-400mg Gabape
- Allergien
- Bell peppers, Okra, Eggplant, Garlic, Onion, Eggs, Caffeine, Theophylline, Glyphosate , Glycerin, PEG, Tylenol, Aspirin it I consume orally, Penicillin, Sulfa, Tetracycline, Valium, Latex, Adhesive, Depo, Progesterone
- Vorherige Impfungen
- Tetanus in 1984 : I could not walk for 3 months.
- Staat
- SC
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 16.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Feeling abnormal
Headache
Myalgia
Symptomtext
Chills; headache; muscle pain; tired; feel bad; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) received via COVID-19 Adverse Event Self-Reporting Solution (COVAES). The reporter is the patient. A 75-year-old male patient received BNT162b2 (BNT162B2), on 06Apr2022 at 15:30 as dose 4 (booster), single (Lot number: FL3209) at the age of 75 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 3, Batch/Lot No: FL3182, Location of injection: Arm Left), administration date: 26Sep2021, when the patient was 75-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: EL9266, Location of injection: Arm Left), administration date: 11Feb2021, when the patient was 74-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EL3249, Location of injection: Arm Left), administration date: 21Jan2021, when the patient was 74-year-old, for COVID-19 immunization. The following information was reported: CHILLS (non-serious) with onset 06Apr2022 at 23:00, outcome "recovered" (Apr2022); FEELING ABNORMAL (non-serious) with onset 06Apr2022 at 23:00, outcome "recovered" (Apr2022), described as "feel bad"; HEADACHE (non-serious) with onset 06Apr2022 at 23:00, outcome "recovered" (Apr2022); MYALGIA (non-serious) with onset 06Apr2022 at 23:00, outcome "recovered" (Apr2022), described as "muscle pain"; FATIGUE (non-serious) with onset 06Apr2022 at 23:00, outcome "recovered" (Apr2022), described as "tired". Therapeutic measures were not taken as a result of chills, headache, myalgia, fatigue, feeling abnormal. Additional information: No other vaccine in four weeks. Patient had no known allergies. No covid prior vaccination. The patient was not tested for covid post vaccination. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 16.04.2022
- Impfdatum
- 21.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Computerised tomogram
Fatigue
Headache
Nausea
Pain in extremity
Vitamin D
Vitamin D decreased
Symptomtext
he had the headache for three to four weeks continuously, very severe; Tiredness; Nausea; Vitamin D level has reduced to 13; bilateral leg pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 14-year-old male patient received BNT162b2 (BNT162B2), on 21Jan2022 as dose 3 (booster), 0.3 ml single (Lot number: FL3209, Expiration Date: 30Jan2022) at the age of 14 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (2nd dose, Lot Number: EW0217, Expiration Date: 30Sep2021, Route, Anatomical Location: Left arm), administration date: 25Jun2021, when the patient was 14-year-old, for covid-19 Immunization; BNT162b2 (1st dose, Lot Number: EW0186, Expiration Date: 31 Aug 2021, Route, Anatomical Location: Left arm), administration date: 04Jun2021, when the patient was 14-year-old, for covid-19 Immunization. The following information was reported: NAUSEA (non-serious) with onset 2022, outcome "unknown"; FATIGUE (non-serious) with onset 2022, outcome "unknown", described as "Tiredness"; VITAMIN D DECREASED (non-serious) with onset 2022, outcome "unknown", described as "Vitamin D level has reduced to 13"; PAIN IN EXTREMITY (non-serious) with onset 2022, outcome "unknown", described as "bilateral leg pain"; HEADACHE (non-serious) with onset 2022, outcome "unknown", described as "he had the headache for three to four weeks continuously, very severe". The event "he had the headache for three to four weeks continuously, very severe" required emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of nausea, vitamin d decreased. Additional information: Reporter wants to know if it is a concern that after a couple of months he is still suffering. The symptoms continuing even after couple of months, symptoms did not stop. After getting the shot, he had symptoms like someone beating his head, he had the headache for three to four weeks continuously, very severe. Like a band of headaches, like band around, feeling like someone hitting him on the back of his head. Headaches started slowly about a week after getting the booster shot. he is getting healed up, now getting the headache on and off. Tiredness like he ran for like three miles, imagine if sprinting. The headache was persistent and now he is feeling the tiredness and nausea. Vitamin D level has reduced to 13, unknown units. Level check on 30Mar2022. Patient is an athlete, he is healthy, he has been an athlete for four years, he practices every week, very healthy child. Symptoms started after booster shot. Exact dates unknown. general lab work seems to be normal. Treatment for Vitamin D with Vitamin D2 Supplement 50,000 IU. Use before 31Mar2023. In an orange pharmacy bottle from the pharmacy. NDC/Lot/Expiration unknown. Treatment for Nausea with Ondansetron 8mg tablets. Caller has a strip of medication. Expires: 2024. B/N: OD0820028A. Lot/NDC unknown. AE required to visit emergency room on 14Feb2022, for the headache, Head CT Scan which was normal, patient was not admitted, he was in the Emergency Room for a few hour. Prior Vaccinations (within 4 weeks) the patient did not received any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s). Patient went to the Neuro doctor, and ENT specialist, all good to go, all the specialists seems to be good, vision specialist, pediatric all seems to be good, patient is still having the issue. Reporter (patient parent) said his question was about the common symptoms that patient has suffered with that he has had issues for two and a half months after his booster dose on 21st of January. Patient still has headache and nausea and tiredness and going on with pain, which is common, but he would like to know how long it would take to complete and also started having bilateral leg pain a week after receiving the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220214; Test Name: CT Scan; Result Unstructured Data: Test Result:Normal; Test Date: 20220330; Test Name: Vitamin D level has reduced to 13, unknown units. Level check on 30 Mar 2022.; Result Unstructured Data: Test Result:Has reduceed to 13
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Relevant Med History:None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Symptomtext
Patient called and reported that she was having body aches in half of her body. She reported no rash, itch, or any swelling/inflammation. Patient was counseled that these were side effects that can happen and the reaction after the second dose can be stronger. Was counseled she could take some Tylenol or ibuprofen and if aches are not going away or getting worse to contact doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Symptomtext
Muscle pain all over her body from head to toe started the day after inoculation. She states it was horrible pain; This is a spontaneous report received from a contactable reporter(s) (Other HCP). A 84 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administration date 31Mar2022 (Lot number: FL3209) at the age of 84 years as dose 4 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Vaccine brand: Pfizer / BioNTech, Vaccine brand unknown: False, Vaccine administration date: 28Sep2021, Vaccine lot number: FF2557, Vaccine lot unknown: False, Vaccine dose number: 3, Vaccine dose number unknown: False, Vaccine location: Left arm), administration date: 28Sep2021, when the patient was 83 years old, for Covid-19 immunization; Bnt162b2 (Vaccine brand: Pfizer / BioNTech, Vaccine brand unknown: False, Vaccine administration date: 27Feb2021, Vaccine administration time: 09:45 AM, Vaccine lot number: EN6198, Vaccine lot unknown: False, Vaccine dose number: 2, Vaccine dose number unknown: False, Vaccine location: Left arm), administration date: 27Feb2021, when the patient was 83 years old, for Covid-19 immunization; Bnt162b2 (Vaccine brand: Pfizer / BioNTech, Vaccine brand unknown: False, Vaccine administration date: 06Feb2021, Vaccine administration time: 02:15 PM, Vaccine lot number: EM9180, Vaccine lot unknown: False, Vaccine dose number: 1, Vaccine dose number unknown: False, Vaccine location: Left arm), administration date: 06Feb2021, when the patient was 83 years old, for Covid-19 immunization. The following information was reported: MYALGIA (non-serious) with onset 02Apr2022, outcome "recovering", described as "Muscle pain all over her body from head to toe started the day after inoculation. She states it was horrible pain". Therapeutic measures were not taken as a result of myalgia. Additional Information: Adverse event: Muscle pain all over her body from head to toe started the day after inoculation. She states it was horrible pain. Today 05Apr2022 she is feeling a bit better. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 05.02.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Rash
Symptomtext
Skin Rash; itching; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 45 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 05Feb2022 (Lot number: FL3209) at the age of 45 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (1st Dose, Date: 10Aug2021, Anatomical site of injection: left arm, Route of administration: Intramuscular, Batch/Lot number: FA7485), administration date: 10Aug2021, when the patient was 45 years old, for Covid-19 immunization, reaction(s): "Flu like symptoms", "skin rash"; Bnt162b2 (2nd Dose, Date: 31Aug2021, Anatomical site of injection: left arm , Route of administration: Intramuscular, Batch/Lot number: FP8448), administration date: 31Aug2021, when the patient was 45 years old, for Covid-19 Immunization, reaction(s): "skin rash itchy only", "skin rash itchy only". The following information was reported: RASH (non-serious) with onset 06Feb2022, outcome "recovered" (2022), described as "Skin Rash"; PRURITUS (non-serious) with onset 06Feb2022, outcome "recovered" (2022), described as "itching". Therapeutic measures were taken as a result of rash, pruritus. Additional information: The patient was treated with Hydrocortisone cream over the counter. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 12.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy skin
Burning sensation
Discomfort
Pruritus
Rash
Rash macular
Skin irritation
Tinnitus
Urticaria
Symptomtext
ringing in her ears; rashes all over her body; hives and blotches in her back and torso; hives and blotches in her back and torso; it's burning in her skin.; The rash started out kind of mild then progressed to more itchy; its irritating and uncomfortable; its irritating and uncomfortable; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from medical information team. A 73 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 12Jan2022 (Lot number: FL3209) at the age of 73 years as dose 3 (booster), single and administration date 29Apr2021 (Lot number: EW0173) as dose 2, single for covid-19 immunisation. Relevant medical history included: "blood pressure" (unspecified if ongoing). Concomitant medication(s) included: BENADRYL. Vaccination history included: Bnt162b2 (Dose: 1, Batch/Lot Number: EW0153, Anatomical Location: Left arm), administration date: 08Apr2021, when the patient was 72 years old, for COVID-19 immunization, reaction(s): "flushing face". The following information was reported: TINNITUS (non-serious), outcome "recovering", described as "ringing in her ears"; RASH (non-serious), outcome "not recovered", described as "rashes all over her body"; URTICARIA (non-serious), RASH MACULAR (non-serious), outcome "unknown" and all described as "hives and blotches in her back and torso"; BURNING SENSATION (non-serious), outcome "unknown", described as "it's burning in her skin."; PRURITUS (non-serious), outcome "unknown", described as "The rash started out kind of mild then progressed to more itchy"; SKIN IRRITATION (non-serious), DISCOMFORT (non-serious), outcome "unknown" and all described as "its irritating and uncomfortable". The events "ringing in her ears", "rashes all over her body", "hives and blotches in her back and torso", "hives and blotches in her back and torso", "it's burning in her skin.", "the rash started out kind of mild then progressed to more itchy", "its irritating and uncomfortable" and "its irritating and uncomfortable" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of tinnitus, rash, urticaria, rash macular, burning sensation, pruritus, skin irritation, discomfort. Additional information: Patient has received 3 doses of the vaccine and she has been experiencing a flushing face, ringing in her ears and rashes all over her body; stating also to have hives and blotches in her back and torso. She mentioned that everytime she puts her clothes on it feels like it is burning in her skin. She went to the dermatologist and she had a biopsy and they told her that this side effects might be due to a medication. She is taking Benadryl and a medication for her blood pressure but they verified if the manufacturer changed the formulation for this medicines and at the end they see most probable that the side effects are due to the vaccine. The patient experienced ringing in the ears and rash after the vaccines. The patient got the first dose on 08Apr2021, and she immediately had flushing in her face. The patient stayed there for 15 -20 minutes until it subsided. Then the patient had ringing in her ears, mostly in her left ear but it went down until 29Apr2021, when she got the second dose, then it increased and she had more ringing. On 12Jan2022, the patient got the booster dose and the ringing of the ears got a little worse, it got better then worse. At first the patient had a rash that was not too prominent but over the last couple of months, since January it was most noticeable. The rash started out kind of mild then progressed to more itchy and has not gone away. The patient has seen a dermatologist and an allergist who prescribed low doses of benadryl and allegra- fexofenadine. At night the patient takes one benadryl and she takes on allegra in the morning. The rash is still there and been there for a couple of months. The rash is aggravated by heat, its irritating, and it bothers the patient when her clothes touch her. The patient has an appointment next week with her allergist. The rash showed up mild at the beginning- it was after the second one or the third dose, it got more prominent after the third. The rash is not responsive to the antihistamines. The patient's symptoms serious criteria is mild to moderate, they are more of a nuisance. After each shot the ringing of the ears got worse and then got better. The rash is the main concern because its irritating and uncomfortable. The patient also now has hives with the rash. The dermatologist did a biopsy and at first she thought it was rosacea pityriasis but it was not. The patient had the biopsy done at and it showed it represents a medicine and medication reaction. This has been going on for a long time. The patient was only taking a blood pressure pill and vitamins when she got her vaccines and stopped them to see if it was and it was not. The dermatologist said it was from the blood pressure pill and she had been on that for years and they hadn't changed the formulation in it in over 10 years and she takes that brand for over 20 years. The patient stopped taking her blood pressure pill about 2 weeks ago. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220126; Test Name: Skin Biopsy; Result Unstructured Data: Test Result:represents a medicine and medication reaction; Comments: Result: represents a medicine and medication reaction; Unit: Not Provided
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure abnormal
- Andere Medikamente
- BENADRYL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Insomnia
Pain
Symptomtext
Pt came in on 3/30/22 (5pm) saying her arm has been hurting since receiving the vaccination and cannot sleep on her arm. When asked to point to the pain, she pointed to the left tricep area. She described the pain as shooting up toward the shoulder, and also down toward the arm/elbow. She said she has taken 1 Tylenol and 1 ibuprofen but it doesn't help. She said she went to a chiropractor and was told she'd need 10 additional treatments. She said she'd try to ice it tonight. She was advised to call her primary care physician tomorrow morning for follow-up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Not known
- Vorgeschichte
- Not known
- Andere Medikamente
- Not known
- Allergien
- Not known
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 30.03.2022
- Impfdatum
- 12.06.2021
- Beginn
- 27.03.2022
- Tage bis Beginn
- 288,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain upper
COVID-19
Chills
Cholecystitis acute
Computerised tomogram abdomen abnormal
Constipation
SARS-CoV-2 test positive
Small intestinal obstruction
Ultrasound biliary tract
Vaccine breakthrough infection
Vomiting
Symptomtext
Covid19 breakthrough. 1st vaccine received on 05/22/2021. 20 y/o male with PMHX of perforated appendicitis s/p open appy in 2017 with small bowel obstruction s/p exp lap and adhesiolysis in 2017. Pt presents with c/o Right upper quadrant abdominal/ epigastric pain that is worsening since the day before. Pt endorses 12 episodes of emesis, chills and constipation. Pt afebrile, GB US shows acute cholecystitis and possible stone in CBD. CT abdomen with Small bowel obstruction. Pt scheduled for colonoscopy/flexible sigmoidoscopy, pre procedure COVID test -positive. Pt afebrile, room air sat 100%. No Covid treatment ordered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- SARS CoV 2 PCR Covid19-Detected on 03/27/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Perforated Appendicitis/open appy, small bowel obstruction s/p exp lap and adhesiolysis
- Andere Medikamente
- -
- Allergien
- No known medication allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 26.03.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Decreased appetite
Fatigue
Product storage error
Symptomtext
PATIENT WAS GIVEN A PFIZER VACCINE-PURPLE CAP THAT WAS SITTING AT ROOM TEMPERATURE FOR MORE THAN 24 HOURS. PATIENT WAS FOLLOWED UP, BUT HAS NO SIGNIFICANT ADVERSE EVENT. SHE DID EXPLAINED THAT SHE FELT TIRE AND HAD NO APPETITE FOR A WEEK, BUT AFTER SHE WAS FINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 26.03.2022
- Impfdatum
- 24.02.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 20,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Symptomtext
This is a spontaneous report received from contactable consumer or other non-HCP. A 44-year-old female patient received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, batch/lot# FL3209), at the age of 44, on Feb 24, 2022, single dose, for COVID-19 immunization. Concomitant medication included simvastatin 20 mg 1x/day for high cholesterol. Medical history included high cholesterol (ongoing). The patient had diarrhea (she has had diarrhea lately), onset Mar 16, 2022, with outcome of unknown. Additional information: Reporter stated her mother got the first dose of the Pfizer-BioNTech COVID-19 vaccine on Feb 24, 2022. She's scheduled to get the second dose on Mar 17, 2022. Her mother is currently using simvastatin and has had diarrhea lately. Reporter would like to know if her mother can get the second dose tomorrow. She was not sure if it was from the vaccine or from the new medication (simvastatin 20mg) the doctor gave her for high cholesterol, which she started a few days ago. No follow-up attempts possible. No further information expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- High cholesterol
- Vorgeschichte
- High cholesterol
- Andere Medikamente
- Simvastatin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Chills
Fatigue
Haematemesis
Cough
Headache
Myalgia
Pain in extremity
Vaccination site pain
Injection site pain
Nasopharyngitis
Pain
Respiratory rate increased
Vomiting
Symptomtext
I was having pain at the site where I had taken the shot; I was having pain in my other shoulder as well all of a sudden; I have been very tired. I was having some tiredness; Headache; Muscle pain; Chills; Joint pain; I throwing my vomit all the day/ all throwing up or whatever vomiting; I am having a lot of pain all of a sudden, I wasn't having the pain like this at first; Breathing very rapidly; Cold; Cough; Chills; Both of my arms hurt; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200334968 (Pfizer). A 57 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 23Feb2022 (Lot number: FL3209) at the age of 57 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Menopause" (unspecified if ongoing), notes: Verbatim: Menopause; "I take my blood pressure pills" (unspecified if ongoing), notes: I take my blood pressure pills; "Arthritis" (unspecified if ongoing), notes: That's what I was taking, not because of the Pfizer, but because of arthritis. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose: 1, Was taking that for pain, like I said I was having pain in my foot and I was having pain in my shoulder/but it wasn't the pain that I am having now), administration date: 01Mar2021, when the patient was 56 years old, for COVID-19 Immunization, reaction(s): "I was having pain in my foot and I was having pain in my shoulder", "I was having pain in my foot and I was having pain in my shoulder"; Bnt162b2 (Dose: 2, Second Pfizer dose), administration date: 23Mar2021, when the patient was 56 years old, for COVID-19 Immunization. The following information was reported: INJECTION SITE PAIN (non-serious) with onset Feb2022, outcome "unknown", described as "I was having pain at the site where I had taken the shot"; ARTHRALGIA (non-serious) with onset Feb2022, outcome "unknown", described as "I was having pain in my other shoulder as well all of a sudden"; FATIGUE (non-serious) with onset Feb2022, outcome "unknown", described as "I have been very tired. I was having some tiredness"; HEADACHE (non-serious) with onset Feb2022, outcome "unknown", described as "Headache"; MYALGIA (non-serious) with onset Feb2022, outcome "unknown", described as "Muscle pain"; CHILLS (non-serious), CHILLS (non-serious) all with onset Feb2022, outcome "unknown" and all described as "Chills"; ARTHRALGIA (non-serious) with onset Feb2022, outcome "unknown", described as "Joint pain"; VOMITING (non-serious) with onset Feb2022, outcome "unknown", described as "I throwing my vomit all the day/ all throwing up or whatever vomiting"; PAIN (non-serious) with onset Feb2022, outcome "unknown", described as "I am having a lot of pain all of a sudden, I wasn't having the pain like this at first"; RESPIRATORY RATE INCREASED (non-serious) with onset Feb2022, outcome "unknown", described as "Breathing very rapidly"; NASOPHARYNGITIS (non-serious) with onset Feb2022, outcome "unknown", described as "Cold"; COUGH (non-serious) with onset Feb2022, outcome "unknown", described as "Cough"; PAIN IN EXTREMITY (non-serious) with onset Feb2022, outcome "unknown", described as "Both of my arms hurt". Therapeutic measures were taken as a result of injection site pain, arthralgia, fatigue, headache, myalgia, chills, arthralgia, vomiting, pain, respiratory rate increased, nasopharyngitis, cough, chills, pain in extremity. No follow-up attempts are possible. No further information is expected. Additional Information: The patient reported that she was having pain at the site where she had taken the shot, she was having pain at that site and also she was having pain in my other shoulder as well all of a sudden and then she had been very tired. She had been having some tiredness. She had been having headache and muscle pain, chills, joint pain and like she was throwing her vomit all the day, Couples of time she had been given like all throwing up or vomiting and she had just been having completely, anyway she had been constantly taking Tylenol. The patient reported that It is the Pfizer, the Pfizer booster because she had already taken the shot, so it was just the booster. The patient reported that she was also kind of like, when she be working or whatever, she was like short 'winded', breathing very rapidly. So the other day so when she was working she kind of have to stop working a couple of times to sit down to get rest. The patient reported that before she took the Pfizer that she was already going through some changes in her body already with cold chills and well she reported that she had cold chills and cough but now have cough, cold, chills, other things different. The patient reported that her shoulders were hurting so bad sometimes. It is not constantly, it's like off and on. Sometimes it hurt, sometimes it don't. But lately it has been hurting when she lay down, when it is cold, it aches, different times it happens. The patient reported that she already had problem from this Feb, before she took booster whatever it was she did not know, but her shoulders were little bit in pain but now is more pain in her shoulders she guessed. But it is not constantly, you know, off and on. The patient reported that she was wondering why she was through so much pain at different time all of a sudden and she started to read the paper. She reported that because she just started reading to the paper and once she started reading the paper, she saw all these things are happening to her. So this is what is going on with her. She reported last time she had taken the other Pfizer was 23Mar. She took one 01Mar2021, 23Mar2021 and then the last one she took 23Feb2022 and she had no other shot other than that. She reported that the arm that she had got hurt before. So that's why she used that arm because she didn't want to use her other arm, just in case anything happens, both of my arms hurt. The patient reported that was taking Tylenol even when she was before she took the other two shots. She was ok when she took the other two shots. It started when she took that shot, so she was not take that shot but went on and took it anyway. So she know she was having side effects. She reported that she was taking Meloxicam for pain and that was when she got the Pfizer, the first Pfizer. That's what she was taking, not because of the Pfizer, but because of arthritis. She was taking that for pain, like she said she was having pain in her foot and was having pain in her shoulder, both shoulders. She was having pain in her shoulders as well but it wasn't the pain that she was having now. She didn't start having the pain till she took that second Pfizer dose. But she didn't look at it as nothing because she just thought it was just normal because it was off and on and I weren't taking Tylenols like that either but now with this here is different. Follow-Up (02Mar2022): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthritis (That's what I was taking, not because of the Pfizer, but because of arthritis); Blood pressure abnormal (I take my blood pressure pills); Menopause (Verbatim: Menopause)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Chills
Fatigue
Haematemesis
Cough
Headache
Myalgia
Pain in extremity
Vaccination site pain
Injection site pain
Nasopharyngitis
Pain
Respiratory rate increased
Vomiting
Symptomtext
I was having pain at the site where I had taken the shot; I was having pain in my other shoulder as well all of a sudden; I have been very tired. I was having some tiredness; Headache; Muscle pain; Chills; Joint pain; I throwing my vomit all the day/ all throwing up or whatever vomiting; I am having a lot of pain all of a sudden, I wasn't having the pain like this at first; Breathing very rapidly; Cold; Cough; Chills; Both of my arms hurt; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200334968 (Pfizer). A 57 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 23Feb2022 (Lot number: FL3209) at the age of 57 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Menopause" (unspecified if ongoing), notes: Verbatim: Menopause; "I take my blood pressure pills" (unspecified if ongoing), notes: I take my blood pressure pills; "Arthritis" (unspecified if ongoing), notes: That's what I was taking, not because of the Pfizer, but because of arthritis. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose: 1, Was taking that for pain, like I said I was having pain in my foot and I was having pain in my shoulder/but it wasn't the pain that I am having now), administration date: 01Mar2021, when the patient was 56 years old, for COVID-19 Immunization, reaction(s): "I was having pain in my foot and I was having pain in my shoulder", "I was having pain in my foot and I was having pain in my shoulder"; Bnt162b2 (Dose: 2, Second Pfizer dose), administration date: 23Mar2021, when the patient was 56 years old, for COVID-19 Immunization. The following information was reported: INJECTION SITE PAIN (non-serious) with onset Feb2022, outcome "unknown", described as "I was having pain at the site where I had taken the shot"; ARTHRALGIA (non-serious) with onset Feb2022, outcome "unknown", described as "I was having pain in my other shoulder as well all of a sudden"; FATIGUE (non-serious) with onset Feb2022, outcome "unknown", described as "I have been very tired. I was having some tiredness"; HEADACHE (non-serious) with onset Feb2022, outcome "unknown", described as "Headache"; MYALGIA (non-serious) with onset Feb2022, outcome "unknown", described as "Muscle pain"; CHILLS (non-serious), CHILLS (non-serious) all with onset Feb2022, outcome "unknown" and all described as "Chills"; ARTHRALGIA (non-serious) with onset Feb2022, outcome "unknown", described as "Joint pain"; VOMITING (non-serious) with onset Feb2022, outcome "unknown", described as "I throwing my vomit all the day/ all throwing up or whatever vomiting"; PAIN (non-serious) with onset Feb2022, outcome "unknown", described as "I am having a lot of pain all of a sudden, I wasn't having the pain like this at first"; RESPIRATORY RATE INCREASED (non-serious) with onset Feb2022, outcome "unknown", described as "Breathing very rapidly"; NASOPHARYNGITIS (non-serious) with onset Feb2022, outcome "unknown", described as "Cold"; COUGH (non-serious) with onset Feb2022, outcome "unknown", described as "Cough"; PAIN IN EXTREMITY (non-serious) with onset Feb2022, outcome "unknown", described as "Both of my arms hurt". Therapeutic measures were taken as a result of injection site pain, arthralgia, fatigue, headache, myalgia, chills, arthralgia, vomiting, pain, respiratory rate increased, nasopharyngitis, cough, chills, pain in extremity. No follow-up attempts are possible. No further information is expected. Additional Information: The patient reported that she was having pain at the site where she had taken the shot, she was having pain at that site and also she was having pain in my other shoulder as well all of a sudden and then she had been very tired. She had been having some tiredness. She had been having headache and muscle pain, chills, joint pain and like she was throwing her vomit all the day, Couples of time she had been given like all throwing up or vomiting and she had just been having completely, anyway she had been constantly taking Tylenol. The patient reported that It is the Pfizer, the Pfizer booster because she had already taken the shot, so it was just the booster. The patient reported that she was also kind of like, when she be working or whatever, she was like short 'winded', breathing very rapidly. So the other day so when she was working she kind of have to stop working a couple of times to sit down to get rest. The patient reported that before she took the Pfizer that she was already going through some changes in her body already with cold chills and well she reported that she had cold chills and cough but now have cough, cold, chills, other things different. The patient reported that her shoulders were hurting so bad sometimes. It is not constantly, it's like off and on. Sometimes it hurt, sometimes it don't. But lately it has been hurting when she lay down, when it is cold, it aches, different times it happens. The patient reported that she already had problem from this Feb, before she took booster whatever it was she did not know, but her shoulders were little bit in pain but now is more pain in her shoulders she guessed. But it is not constantly, you know, off and on. The patient reported that she was wondering why she was through so much pain at different time all of a sudden and she started to read the paper. She reported that because she just started reading to the paper and once she started reading the paper, she saw all these things are happening to her. So this is what is going on with her. She reported last time she had taken the other Pfizer was 23Mar. She took one 01Mar2021, 23Mar2021 and then the last one she took 23Feb2022 and she had no other shot other than that. She reported that the arm that she had got hurt before. So that's why she used that arm because she didn't want to use her other arm, just in case anything happens, both of my arms hurt. The patient reported that was taking Tylenol even when she was before she took the other two shots. She was ok when she took the other two shots. It started when she took that shot, so she was not take that shot but went on and took it anyway. So she know she was having side effects. She reported that she was taking Meloxicam for pain and that was when she got the Pfizer, the first Pfizer. That's what she was taking, not because of the Pfizer, but because of arthritis. She was taking that for pain, like she said she was having pain in her foot and was having pain in her shoulder, both shoulders. She was having pain in her shoulders as well but it wasn't the pain that she was having now. She didn't start having the pain till she took that second Pfizer dose. But she didn't look at it as nothing because she just thought it was just normal because it was off and on and I weren't taking Tylenols like that either but now with this here is different. Follow-Up (02Mar2022): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthritis (That's what I was taking, not because of the Pfizer, but because of arthritis); Blood pressure abnormal (I take my blood pressure pills); Menopause (Verbatim: Menopause)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 28,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cellulitis
Herpes zoster
Injection site erythema
Injection site pain
Injection site warmth
Symptomtext
Woke up with pain on my left arm/ inside left elbow/forearm. Intense pain as if it was an internal injury. No bruising or outside the skin injury. Then it started to have redness & feel warm to the touch. I?ve had similar symptoms with shingles in 2010, so I went to the urgent care clinic earlier this week and they started me on medication for shingles and/or cellulitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Had Shingles in 2010
- Andere Medikamente
- Fluoxetine 60mg/day
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 22.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ocular hyperaemia
Pruritus
Rhinorrhoea
Sensation of foreign body
Tryptase
Symptomtext
30yo M with PMH concerning for possible allergy to PEG. Because of this further evaluation was undergone with SPT to PEG330. Patient was found to be reactive to 170mg/ml on testing. Given this and his prior reaction to the bowel prep I discussed with patient that this likely represents a true allergy. We discussed next steps moving forward such as the risks/benefits of receiving a booster dose of the COVID-19 mRNA vaccine (Pfizer). After discussion of possible risks of anaphylaxis despite him tolerating 2 doses of the vaccine previously we decided that the benefits outweighed the risks of proceeding with the vaccine. After receiving the vaccine he remained asymptomatic for the first 15 minutes. After that he developed a globus sensation in his throat and some subjective itchiness of the hand/scalp. VS were taken at that time which were normal and no objective symptoms were noted. About 10 minutes later patient endorses some diffuse pruritus, with objective rhinorrhea and conjunctival erythema. At that time we administered 0.3mg of epinephrine via EAI into the anterolateral left thigh. Patient was subsequently given an OAH Zyrtec 10mg. 10 minutes after receiving the epinephrine patient endorsed resolution of the pruritus and conjunctival erythema as well as improvement in the globus sensation. 10 minutes later the globus sensation had completely resolved. throughout this time lungs remained CTAB with no urticaria noted and stable vital signs throughout. Patient was observed for an hour after resolution of symptoms and discharged home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Tryptase drawn day of reaction: 7.5
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- hematochezia
- Andere Medikamente
- none
- Allergien
- Polyethylene Glycol
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 06.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Confusional state
Dizziness
Menstrual disorder
Symptomtext
I'm still light headed, dizzy, and a little confused sometimes.; I'm still light headed, dizzy, and a little confused sometimes.; I'm still light headed, dizzy, and a little confused sometimes.; The second round was 3 days ago; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 29 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 06Feb2022 11:30 (Lot number: fl3209) at the age of 29 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "known allergies: Avocado" (unspecified if ongoing); "Bipolar 2" (unspecified if ongoing); "Depression" (unspecified if ongoing); "GAD" (unspecified if ongoing); "PMDD" (unspecified if ongoing); "Arthritis" (unspecified if ongoing). Concomitant medication(s) included: LAMICTAL. Vaccination history included: Bnt162b2 (Dose 1, Single, lot number: FJ5682,, administration time: 10:30AM, vaccine location: Left arm), administration date: 16Jan2022, when the patient was 29 years old, for COVID-19 Immunization, reaction(s): "monthly cycle started 2 weeks early, was much worse than usual, experienced excessive blood clots with the first round", "monthly cycle started 2 weeks early, was much worse than usual, experienced excessive blood clots with the first round", "Light headed/dizzy", "A little confused sometimes". The following information was reported: DIZZINESS (non-serious), DIZZINESS (non-serious), CONFUSIONAL STATE (non-serious) all with onset Feb2022, outcome "not recovered" and all described as "I'm still light headed, dizzy, and a little confused sometimes."; MENSTRUAL DISORDER (non-serious) with onset Feb2022, outcome "unknown", described as "The second round was 3 days ago". Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthritis; Bipolar II disorder; Depression; Fruit allergy; Gadolinium deposition disease; Premenstrual dysphoric disorder
- Andere Medikamente
- LAMICTAL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear pain
Tinnitus
Symptomtext
Horrific shooting pain in her right ear/it felt like a needle in her ear; Tinnitus; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). A 75 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 08Jan2022 14:15 (Lot number: FL3209) at the age of 75 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (First Dose, Lot: EM9806, Expiration: unknown), administration date: 10Feb2021, when the patient was 74 years old, for COVID-19 Immunization, reaction(s): "She did not have reactions on first two doses"; Bnt162b2 (Second dose, Lot: EN6205, Expiration: unknown), administration date: 03Mar2021, when the patient was 74 years old, for COVID-19 Immunization, reaction(s): "She did not have reactions on first two doses". The following information was reported: EAR PAIN (non-serious) with onset 09Jan2022, outcome "recovered" (2022), described as "Horrific shooting pain in her right ear/it felt like a needle in her ear"; TINNITUS (non-serious) with onset 09Jan2022, outcome "not recovered", described as "Tinnitus". Therapeutic measures were not taken as a result of ear pain, tinnitus. Additional information: There were other products and investigation assessment reported. She never had any pain in her ear ever. That pain lasted a minute and knew something was very wrong, it was coincident to the shot. Tinnitus started very shortly after that. No additional vaccines were administered on the same date of the Pfizer suspect. AE(s) did not require a visit to Emergency Room and Physician Office. The patient did not receive any vaccine, prior vaccination (within 4 weeks). There was no AE(s) following prior vaccinations. It was reported, thousands and thousands, over 13,000 people have reported the exact same thing, not just tinnitus, it occurred in a certain time frame, certain tone and escalated after subsequent doses. She was asking why isn't Pfizer is not sharing this. No follow-up attempts are possible. No further information is expected. Follow-Up (04FEB2022): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 19.03.2022
- Impfdatum
- 07.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Autoimmune disorder
Chills
Malaise
Vulval ulceration
Vulvovaginal pain
Symptomtext
This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. The following information was reported: AUTOIMMUNE DISORDER (medically significant) with onset Jan2022, outcome "unknown", described as "autoimmune reaction"; VULVAL ULCERATION (medically significant) with onset Jan2022, outcome "unknown", described as "vulvar aphthous ulcer"; VULVOVAGINAL PAIN (medically significant) with onset Jan2022, outcome "unknown", described as "didn't want to pee because it was excruciatingly painful"; MALAISE (non-serious) with onset Jan2022, outcome "unknown", described as "not feeling well"; CHILLS (non-serious), outcome "unknown", described as "Shivers". The events "autoimmune reaction", "vulvar aphthous ulcer" and "didn't want to pee because it was excruciatingly painful" were evaluated at the physician office visit. Therapeutic measures were taken as a result of autoimmune disorder, vulval ulceration, vulvovaginal pain. Patient had an autoimmune reaction called vulvar aphthous ulcer. Patient had like canker sores the size of a thumbnail, huge open raw wounds in her vaginal area. Reporter considered it a non sexually acquired ulcer, and it is best described as like a canker sore. Patient got a vaccine on a Friday, and then on Monday she started not feeling well, and she thought she had contracted COVID, because simultaneously they got contacted from the school who said she may have been exposed to someone in her class at school who tested positive. Patient also had shivers and didn't feel well, but had no fever. She tested the next day on Tuesday, which was negative for the first one where it was a nose test and they swabbed her then 20 minutes later had results, the rapid test. They had to wait two days for the one that goes to the lab, and actually she had two of those that were sent to the lab, one by the school, in case the rapid test was a false negative. She says then on Thursday she tried to get ahold of OBGYN but she was booked out and they asked if it was ok for her daughter to see a nurse. She says the way her daughter was describing it was that her labia was shredded. She says she took her daughter in, but the nurse didn't know, then Thursday evening they called the on call, physician and he saw her Friday. She says by this time patient didn't want to pee because it was excruciatingly painful. She says the doctor showed her a picture and explained that it was outside of her when she asked where the sores were, whether they were on the labia or inside the vagina, and the doctor called it a vulvar ulcer. Nurse had prescribed antibiotics, and then the doctor prescribed an antiviral, and had samples sent in for testing. Patient was not sexually active, but they had to test for herpes and all that, so they were waiting then got results of test. By Friday night her daughter was in so much pain, she didn't want to pee with there being open wounds in her vaginal area. She says when her daughter went to the bathroom to go urinate, the way she described the pain of on a 1-10 scale, ten being most painful, as so excruciating. and incredibly painful. Caller says her daughter took one dose of antibiotics, which she still has at home, but she happens to be at work and doesn't remember what that is called. She says she didn't want her daughter to become antibiotic resistant, so she didn't take it that night while they waited for her to see the doctor, to see what he says. She says other treatments her daughter did was soaking in the tub, and they tried everything, including Vaseline, and she was in so much pain they called that evening.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Dasetta 1/35
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Abdominal pain upper
Arthralgia
Diarrhoea
Flatulence
Illness
Milk allergy
Movement disorder
Musculoskeletal discomfort
Musculoskeletal stiffness
Nausea
Symptomtext
diarrhea; stomach pains; gas pain; I would get sick; I have developed a dairy allergy/lactose intolerant dairy allergy; extreme gastrointestinal stress; nausea; The shoulder of the arm where shot was administered is also in extreme discomfort; It is so stiff; Range of motion is extremely limited on my left side./My range of motion is limited and in the mornings, I can barely lift it; my shoulder was sore/ shoulder pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 03Jan2022 15:00 (Lot number: Fl3209) at the age of 30 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: Sulfa drugs" (unspecified if ongoing); "Known allergies: red 40 food dye" (unspecified if ongoing), notes: Known allergies: red 40 food dye. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: Ew0167, Location of injection: Arm Left, Vaccine Administration Time: 08:00 AM, 1st Dose, Date: 10May2021, Time: 8:00 , Anatomical site of injection: arm/shoulder, Route of administration: Intramuscular, Batch/Lot number: EW0167), administration date: 10May2021, when the patient was 30 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: Ew0191, Location of injection: Arm Left, Vaccine Administration Time: 08:00 AM, 2nd Dose, Date: 01Jun2021, Time: 8:00 , Anatomical site of injection: arm/shoulder , Route of administration: Intramuscular, Batch/Lot number: EW0191), administration date: 01Jun2021, when the patient was 30 years old, for COVID-19 Immunization. The following information was reported: MILK ALLERGY (non-serious) with onset 05Jan2022, outcome "not recovered", described as "I have developed a dairy allergy/lactose intolerant dairy allergy"; ABDOMINAL DISCOMFORT (non-serious) with onset 05Jan2022, outcome "not recovered", described as "extreme gastrointestinal stress"; NAUSEA (non-serious) with onset 05Jan2022, outcome "not recovered", described as "nausea"; MUSCULOSKELETAL DISCOMFORT (non-serious) with onset 05Jan2022, outcome "not recovered", described as "The shoulder of the arm where shot was administered is also in extreme discomfort"; ARTHRALGIA (non-serious) with onset 03Jan2022 15:00, outcome "recovering", described as "my shoulder was sore/ shoulder pain"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 05Jan2022, outcome "not recovered", described as "It is so stiff"; MOVEMENT DISORDER (non-serious) with onset 05Jan2022, outcome "not recovered", described as "Range of motion is extremely limited on my left side./My range of motion is limited and in the mornings, I can barely lift it"; DIARRHOEA (non-serious), outcome "unknown", described as "diarrhea"; ABDOMINAL PAIN UPPER (non-serious), outcome "unknown", described as "stomach pains"; FLATULENCE (non-serious), outcome "unknown", described as "gas pain"; ILLNESS (non-serious), outcome "unknown", described as "I would get sick". Therapeutic measures were taken as a result of milk allergy, arthralgia. Therapeutic measures were not taken as a result of abdominal discomfort, nausea, musculoskeletal discomfort, musculoskeletal stiffness, movement disorder. Additional information :No any other vaccines within 4 weeks prior to the COVID, no prior to vaccination the patient diagnosed with COVID-19, no Since the vaccination the patient had been tested for COVID-19.Prior vaccination, concomitant drugs, patient's medical history, relevant tests, specific relevant test for thromboembolic events with thrombocytopenia was reported as none. treatment include anti-inflammatory medication and diet Change for event shoulder pain and lactose intolerant dairy allergy No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Reaction to food additive (Known allergies: red 40 food dye); Sulfonamide allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 04.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Overdose
Pain in extremity
Product administered to patient of inappropriate age
Pyrexia
Symptomtext
0.3mL dose of the vaccine was given to a 9-year old patient; 0.3mL dose of the vaccine was given to a 9-year old patient; Low grade fever; Sore arm; This is a spontaneous report received from contactable reporter(s) (Pharmacist) from medical information team for a Pfizer sponsored program. A 9 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 04Feb2022 (Lot number: FL3209, Expiration Date: Jun2022) at the age of 9 years as dose 1 (tris), 0.3 ml single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious), OVERDOSE (non-serious) all with onset 04Feb2022, outcome "unknown" and all described as "0.3mL dose of the vaccine was given to a 9-year old patient"; PYREXIA (non-serious) with onset Feb2022, outcome "unknown", described as "Low grade fever"; PAIN IN EXTREMITY (non-serious) with onset Feb2022, outcome "unknown", described as "Sore arm". No follow-up attempts are possible. No further information is expected. Additional information: Caller was calling regarding the Pfizer covid 19 purple cap vaccine. Caller stated that a 0.3mL dose of the vaccine was given to a 9-year old patient last Friday, 04Feb2022. Caller was asking if there was information on how long to wait to give the second dose, or if a second dose was still needed. Caller was asking if there would be any complication that would arise from the patient have a higher-than-authorized dose? Follow-up (08Feb2022, 09Feb2022): This is a follow-up spontaneous report from a Pfizer sponsored program. A contactable pharmacist reported for a 9-year-old female patient that: Updated information: New reporter was added. Patient initials, DOB, age, ethnicity was added. Relevant medical history was added. Vaccination start, stop date, lot number, expiry date, anatomical location was added. Events was added. Concomitant therapy was added. Details: NDC number of Covid vaccine: 59267-1000-1. No investigation assessment. Patient height and weight was unknown.Caller states this dose was given to the patient on 04Feb2021, wants to know when the patient should get her second dose. States she called to check on the patient, states she just has a low grade fever and sore arm from the shot that was reported to the caller by her parents but states she is fine other than that. Email address is confirmed with the caller. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: patient history-No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Pain
Vertigo
Symptomtext
coughing nonstop; full body pains; Vertigo; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 23 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 01Feb2022 12:15 (Lot number: FL3209) at the age of 23 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Depression" (unspecified if ongoing); "Covid-19" (unspecified if ongoing), notes: If covid prior vaccination: Yes. Concomitant medication(s) included: ZOLOFT; JUNEL. Vaccination history included: Bnt162b2 (Dose 2, single, lot number=EW0191,, dose administrator route=Intramuscular,, vaccine location=Right arm), administration date: 16Jun2021, when the patient was 22 years old, for Covid-19 immunization; Bnt162b2 (Dose 1, single, lot number=EW0186,, dose administrator route=Intramuscular,, vaccine location=Right arm), administration date: 26May2021, when the patient was 22 years old, for Covid-19 immunization. The following information was reported: COUGH (non-serious) with onset 01Feb2022 22:00, outcome "recovering", described as "coughing nonstop"; PAIN (non-serious) with onset 01Feb2022 22:00, outcome "recovering", described as "full body pains"; VERTIGO (non-serious) with onset 01Feb2022 22:00, outcome "recovering", described as "Vertigo". Therapeutic measures were not taken as a result of cough, pain, vertigo. Additional Information: The patient has no reported allergies. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. After my booster shot (shot 3) I've been coughing nonstop and having full body pains as well as vertigo. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (If covid prior vaccination: Yes); Depression
- Andere Medikamente
- ZOLOFT; JUNEL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 12.03.2022
- Impfdatum
- 12.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anti-thyroid antibody increased
Anti-thyroid antibody positive
Basedow's disease
Blood thyroid stimulating hormone decreased
Fatigue
Goitre
Hyperthyroidism
Loss of personal independence in daily activities
Thyroxine free
Tri-iodothyronine free
Ultrasound thyroid abnormal
Symptomtext
I diagnosed with Grave's disease and acute Hashimoto's thyrotoxicosis based upon lab drawn on 2/17/2022 He presented with fatigue and activity intolerance which had progressed in the weeks since he received Pfizer COVID 19 vaccine at a pharmacy. Both anti-thyroid peroxidase antibody and thyrotropin receptor antibodies were significantly elevated. Thyroid ultrasound with diffuse enlargement and hypervascularity He is currently prescribed beta-blocker and methimazole and will follow-up for lab and with his primary care provider. He also has been referred to endocrinology and that visit is scheduled
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- lab from 2/17/2022: TSH = < 0.0008 (0.4 - 4.0) free T4 = 4.41 (0.84 - 1.51) Lab from 2/21/22: free T3 = 17.8 (2.3 -4.2) TPO Ab = 6,178 (0 - 60) TSH receptor (TR) Ab = 7.21 (<1.75)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 09.03.2022
- Impfdatum
- 10.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure increased
Blood test
Electrocardiogram
Headache
Symptomtext
Blood pressure dramatically increased to 177/115 at its highest. Symptoms were headache?s. No other symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Blood tests, ECG,
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High Cholesterol
- Andere Medikamente
- Simvastatin- 20mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 30.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Arthralgia
Blood immunoglobulin A
Blood thyroid stimulating hormone decreased
Blood urine present
C-reactive protein increased
Culture urine positive
Decreased appetite
Eye swelling
Full blood count
Gait disturbance
Henoch-Schonlein purpura
International normalised ratio normal
Klebsiella test positive
Laboratory test
Oral contusion
Platelet count increased
Protein urine present
Symptomtext
Henoch Schonlein purpura with associated bilateral purpuric rash on lower legs, bilateral knee arthralgia with associated algic gait, bruising of gums, swollen eyes, abdominal pain with appetite loss
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Labs and Imaging (from 2/18/2022) TSH 1.640 T4, Free 1.40 UA:WBC >30 hpf, RBC 3-10/hpf, small blood, trace protein, cloudy urine, trace esterase, trace ketones, trace occult blood-urine blood urine culture: Klebsiella pneumoniae CBC: platelets 463 CRP: 8 (ref range 0-10) INR: 1 (ref range 0.9-1.2) ESR: 10 (ref range 0-15) IgA: 323 (ref range 90-386) U/S: showed no clots
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypothyrodism austism spectrum IBS
- Andere Medikamente
- clonidine, escitalopram, esomeprazole, levothyroxine, lorazepam
- Allergien
- peanut and tree nut
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 23.01.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Radiculitis brachial
Symptomtext
Acute shoulder pain in the arm vaccine was received. Evaluated by 2 different Orthopaedics - both with same diagnosis- brachial neuritis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Exposure during pregnancy
Lip swelling
Vomiting
Symptomtext
Per pharmacist, patient is pregnant and came in for her second Pfizer dose. About 30 minutes after receiving the shot, the patient experienced a reaction. She was throwing up and her lips were swollen. She went to the emergency room and was given Zofran, Epi-Pen, and Benadryl. Patient reported feeling better after the pharmacist followed up with her.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Feeling abnormal
Headache
Symptomtext
Patient came to clinic today for other reasons; however, reported having a poking sensation 15 minutes post-vaccination to left chest wall. Afterward, she developed daily headaches, brain fog and severe fatigue, which remain ongoing today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism, depression, GERD
- Andere Medikamente
- Levothyroxine, Omeprazole, Citalopram
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Malaise
Menopause
Menstrual disorder
Pyrexia
Vomiting
Symptomtext
01/28/2022 Vaccination at 11am Drove home. Was just about to sit down and eat, overwhelming sensation of sickness, vomited 3x. Malaise/fatigue rest of the day, feverish. 01/29/2022 Woke up with menstrual cycle and I haven't had for over a year. Menopausal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Scheduled for labs with cardiologist 03/2022
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- allergies COVID 2022; elevated D-dimer
- Andere Medikamente
- Daily Vitamins
- Allergien
- penicillin
- Vorherige Impfungen
- possible flu shot; late 90's
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Testicular pain
Symptomtext
report of testicular pain lasting 15 minutes 30 minutes after vaccine administration. Pain self resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Testicular pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 19.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Illness
Influenza like illness
Pain in extremity
Product use issue
Symptomtext
massive joint pain; severe pain in both calves; severe sickness mimicing the flu for >1 week; severe sickness mimicing the flu for >1 week; flare of arthritis; other vaccine same date product=Prevnar; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 27Jan2022 (Lot number: FL3209) at the age of 49 years as dose 3 (booster), single for covid-19 immunisation; pneumococcal vaccine conj 7v (crm197) (PREVNAR), administered in arm left, administration date 27Jan2022 (Batch/Lot number: unknown) as dose 1, single for immunisation. Relevant medical history included: "Spondoloarthritis" (unspecified if ongoing); "Heart Disease" (unspecified if ongoing); "known allergies DAIRY" (unspecified if ongoing). Concomitant medication(s) included: PLAVIX; REPATHA; ASPIRIN [ACETYLSALICYLIC ACID]; HUMIRA; VIBERZI; SINGULAIR. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE., Batch/Lot No: EN6199, Location of injection: Arm Left), administration date: 27Mar2021, when the patient was 48 years old, for COVID-19 Immunization, reaction(s): "administration date: 27Mar2021, prev dose dose number: 2; prev dose administration date: 27Jan2021, prev dose dose number: 1"; Bnt162b2 (DOSE 1, SINGLE., Batch/Lot No: EN6201, Location of injection: Arm Left), administration date: 27Jan2021, when the patient was 48 years old, for COVID-19 Immunization. The following information was reported: ARTHRALGIA (non-serious) with onset 28Jan2022, outcome "not recovered", described as "massive joint pain"; PAIN IN EXTREMITY (non-serious) with onset 28Jan2022, outcome "not recovered", described as "severe pain in both calves"; ILLNESS (non-serious), INFLUENZA LIKE ILLNESS (non-serious) all with onset 28Jan2022, outcome "not recovered" and all described as "severe sickness mimicing the flu for >1 week"; ARTHRITIS (non-serious) with onset 28Jan2022, outcome "not recovered", described as "flare of arthritis"; PRODUCT USE ISSUE (non-serious) with onset 27Jan2022, outcome "unknown", described as "other vaccine same date product=Prevnar". The events "massive joint pain", "severe pain in both calves", "severe sickness mimicing the flu for >1 week", "severe sickness mimicing the flu for >1 week" and "flare of arthritis" were evaluated at the physician office visit. It was unknown if therapeutic measures were taken as a result of arthralgia, pain in extremity, illness, influenza like illness, arthritis. Additional information:Reported events included trying to get into a Dr. for evaluation massive joint pain, forearm pain, severe pain in both calves, severe sickness mimicking the flu for >1 week; flare of arthritis. Events resulted in doctor or other healthcare professional office/clinic visit. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Device date was reported as 07Feb2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Dairy intolerance; Heart disease, unspecified; Spondylarthritis
- Andere Medikamente
- PLAVIX; REPATHA; ASPIRIN [ACETYLSALICYLIC ACID]; HUMIRA; VIBERZI; SINGULAIR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: ja
Body temperature
Chills
Cough
Diarrhoea
Pyrexia
Vomiting
Symptomtext
Saturday, 29Jan2022, started violently vomiting; diarrhea; teeth were chattering; Friday night, 28Jan2022, started coughing a lot; Had normal onset of fever; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 41 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 28Jan2022 (Lot number: FL3209) at the age of 41 years as dose 3 (booster) single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 1; lot: EK5730; single; Route of administration: left arm), administration date: 18Dec2020, when the patient was 39 years old, for COVID-19 immunization; Bnt162b2 (Dose: 2; lot: EL3246; single; Route of administration: left arm), administration date: 08Jan2021, when the patient was 39 years old, for COVID-19 immunization. The following information was reported: COUGH (medically significant) with onset 28Jan2022, outcome "recovered" (31Jan2022), described as "Friday night, 28Jan2022, started coughing a lot"; PYREXIA (disability) with onset 28Jan2022, outcome "unknown", described as "Had normal onset of fever"; VOMITING (disability) with onset 29Jan2022, outcome "unknown", described as "Saturday, 29Jan2022, started violently vomiting"; DIARRHOEA (disability) with onset 29Jan2022, outcome "unknown", described as "diarrhea"; CHILLS (non-serious) with onset 28Jan2022, outcome "unknown", described as "teeth were chattering". The patient underwent the following laboratory tests and procedures: body temperature: (28Jan2022) 102 Fahrenheit. Therapeutic measures were taken as a result of pyrexia. Clinical course details: The patient's teeth were chattering and had completely like fever like symptoms. Couldn't get out of bed 29Jan2022 or Sunday, 30Jan2022, pretty bad. The patient took Tylenol for fever. Reaction assessed: Diarrhea, Cough, Vomiting, Fever Source of assessment: Primary Source Reporter Method of assessment: Global Introspection Drug related: Related; Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal relationship between the reported events and suspect drug BNT162B2 cannot be excluded. 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.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220128; Test Name: fever; Result Unstructured Data: Test Result:102 Fahrenheit
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 18.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Rash
Skin irritation
Symptomtext
Broke out in a rash that became very irritated and itchy .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site mass
Injection site pain
Injection site pruritus
Symptomtext
Patient developed right arm lump where she received the Flucelvax and COVID-19 vaccine. It has been painful and itching since day of administration (approximately 1 month at this point).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site mass
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Flonase nasal spray
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Muscle spasms
Nausea
Urinary incontinence
Vomiting
Symptomtext
Severe chills and loss of bladder control. Nausea and vomiting for two weeks after shot. Muscles spasms so severe I thought my back was going to break.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Multiple Sclerosis, Celiac Sprue, Hypothyroidism
- Andere Medikamente
- Acyclovir, Baclofen, Donepezil, Famotidine, Fenofibric DR, Fluoxetine, Gabapentin, Lorazepam, Rituxan IV, Rosuvastin Calcium, Sucralfate, Tirosint, OTC: Aspirin, Biotin, Calcium Plus D, Co-Q 10, Cod Liver Oil, Liver Health Formula, Prebioti
- Allergien
- Gluten, Amitriptyline, Ibprophen, Benadryl, Memantine HCL
- Vorherige Impfungen
- Nausea and vomiting, unable to keep food down for three weeks, fever that spiked at 105. Age 56, 12/14/2021 Pfizer Covid-19 dose
- Staat
- -
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Axillary pain
Chills
Fatigue
Headache
Myalgia
Pyrexia
Vaccination site pain
Symptomtext
severe chills; fever; muscle aches; headache; fatigue; intense pain near underarm and shoulder on injection site side; intense pain near underarm and shoulder on injection site side; intense pain near underarm and shoulder on injection site side; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 24 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 18Jan2022 (Lot number: FL3209) at the age of 24 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (dose 2, Lot EW0186, administered in right arm), administration date: 20May2021, when the patient was 23 years old, for Covid-19 immunization; Bnt162b2 (dose 1 , Lot EW0170, administered in left arm), administration date: 29Apr2021, when the patient was 23 years old, for Covid-19 immunization. The following information was reported: CHILLS (non-serious) with onset 18Jan2022, outcome "recovered", described as "severe chills"; PYREXIA (non-serious) with onset 18Jan2022, outcome "recovered", described as "fever"; MYALGIA (non-serious) with onset 18Jan2022, outcome "recovered", described as "muscle aches"; HEADACHE (non-serious) with onset 18Jan2022, outcome "recovered", described as "headache"; FATIGUE (non-serious) with onset 18Jan2022, outcome "recovered", described as "fatigue"; AXILLARY PAIN (non-serious), ARTHRALGIA (non-serious), VACCINATION SITE PAIN (non-serious) all with onset 18Jan2022, outcome "recovered" and all described as "intense pain near underarm and shoulder on injection site side". Therapeutic measures were not taken as a result of chills, pyrexia, myalgia, headache, fatigue, axillary pain, arthralgia, vaccination site pain. Additional Information: The patient received the vaccine at a pharmacy or drug store. The patient did not received any other vaccine within four weeks of the vaccine. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Body temperature
Chills
Flatulence
Interchange of vaccine products
Joint swelling
Off label use
Pain
Pyrexia
Swelling
Symptomtext
gas; bloating with absolutely everything I ate; swelling under my rib cage but it is getting milder; I also had the common side effects of chills, fever (99-100), aching; I also had the common side effects of chills, fever (99-100), aching; I also had the common side effects of chills, fever (99-100), aching; The joints on the injection side are still a bit swollen; The shot was a booster for my previous J&J shot; The shot was a booster for my previous J&J shot; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 03Jan2022 12:00 (Lot number: FL3209) at the age of 57 years as dose number unknown (booster), single for covid-19 immunisation. Relevant medical history included: "Ankylosing spondylitis" (unspecified if ongoing); "Hashimoto's Thyroiditis" (unspecified if ongoing); "Cushings Disease" (unspecified if ongoing); "pituitary origin" (unspecified if ongoing), notes: pituitary origin, in remission without, medication or surgery. Concomitant medication(s) included: LEVOTHYROXINE; SPIRONOLACTONE; ATORVASTATIN. Past drug history included: Remicade, reaction(s): "allergies: Remicade"; Humira, reaction(s): "Allergies:Humira". Vaccination history included: J&j shot (The shot was a booster for my, previous J&J shot), for Covid-19 immunization. The following information was reported: OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 03Jan2022 12:00, outcome "unknown" and all described as "The shot was a booster for my previous J&J shot"; FLATULENCE (non-serious) with onset 04Jan2022, outcome "not recovered", described as "gas"; ABDOMINAL DISTENSION (non-serious) with onset 04Jan2022, outcome "not recovered", described as "bloating with absolutely everything I ate"; SWELLING (non-serious) with onset 04Jan2022, outcome "not recovered", described as "swelling under my rib cage but it is getting milder"; CHILLS (non-serious), PYREXIA (non-serious), PAIN (non-serious) all with onset 04Jan2022, outcome "not recovered" and all described as "I also had the common side effects of chills, fever (99-100), aching"; JOINT SWELLING (non-serious) with onset 04Jan2022, outcome "not recovered", described as "The joints on the injection side are still a bit swollen". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of flatulence, abdominal distension, swelling, chills, pyrexia, pain, joint swelling. Additional Information: Dose Received:1, dose number=1. No other vaccine in four weeks. The shot was a booster for her previous J&J shot. About 36 hours after the shot she began getting severe abdominal cramping, gas and bloating with absolutely everything she ate. Dairy and any type of green chiles were the worst causing horrible smelling flatulence, she NEVER had any kind of dairy allergy or intolerance to spicy food (Thai, New Mexican, Indian, etc). It is 22Jan2022 and she was still having some cramping and swelling under her rib cage but it was getting milder. She felt like the booster threw off her gut flora. She also had the common side effects of chills, fever (99-100), aching, etc along with a pretty bad autoimmune flare-up. The joints on the injection side are still a bit swollen but this should resolve when she start Cosentyx on 27Jan2022. No covid prior vaccination and no covid tested post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Name: fever (99-100); Result Unstructured Data: Test Result:(99-100); Comments: fever (99-100)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Ankylosing spondylitis; Cushings syndrome; Hashimoto's thyroiditis; Pituitary disorder (pituitary origin, in remission without medication or surgery)
- Andere Medikamente
- LEVOTHYROXINE; SPIRONOLACTONE; ATORVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
4 days after the third dose , I have strong hives in my entire body legs, arms, belly and back. The hives didn't go way; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 46 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 14Jan2022 14:45 (Lot number: FL3209) at the age of 46 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Surgical menopause" (unspecified if ongoing); "hypercholesterolemia" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose Number: 1, Batch/Lot No: EL9261, Location of injection: Arm Left, MANUFACTURER UNKNOWN), administration date: 22Jan2021, when the patient was 46 years old, for Covid-19 immunization; Covid-19 vaccine (Dose Number: 2, Batch/Lot No: EN6203, Location of injection: Arm Left, Vaccine Administration Time: 02:00 PM, MANUFACTURER UNKNOWN, After the second dose I started to have sporadically. I thought that was some allergies. I went to the doctor,, did some exames and everything is normal.), administration date: 25Feb2021, when the patient was 46 years old, for Covid-19 immunization, reaction(s): "I started to have sporadically. I thought that was some allergies.". The following information was reported: URTICARIA (non-serious) with onset 18Jan2022, outcome "not recovered", described as "4 days after the third dose , I have strong hives in my entire body legs, arms, belly and back. The hives didn't go way". The event "4 days after the third dose , i have strong hives in my entire body legs, arms, belly and back. the hives didn't go way" was evaluated at the physician office visit. Therapeutic measures were taken as a result of urticaria. Additional information: Vaccine facility type was hospital. Other vaccine in four weeks reported as no. 4 days after the third dose, patient had strong hives in her entire body: legs, arms, belly and back. The hives didn't go way. She searched and she found person with the same hives due vaccine allergies. Ae treated with Zyrtec. Covid prior vaccination and covid tested post vaccination reported as no. Patient had no known allergies. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypercholesterolemia; Surgical menopause
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 46,0
- Geschlecht
- U
- Eingang
- 12.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Immunisation
Lymph node pain
Lymphadenopathy
Vaccination site pain
Symptomtext
Painful swelling of lymph nodes under arm & into breast tissue; Dizziness; Light-headedness when standing; Booster; Pain at injection site; Painful swelling of lymph nodes under arm & into breast tissue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (COMIRNATY), intramuscular, administered in deltoid left, administration date 12Jan2022 16:30 (Lot number: FL3209) at the age of 46 years as dose numner unknown (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Manufacturer- Unknown, Dose number unknown), for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 12Jan2022 16:30, outcome "unknown", described as "Booster"; VACCINATION SITE PAIN (non-serious) with onset Jan2022, outcome "unknown", described as "Pain at injection site"; LYMPHADENOPATHY (non-serious) with onset 20Jan2022, outcome "recovered" (24Jan2022), LYMPH NODE PAIN (non-serious) with onset Jan2022, outcome "recovered" (24Jan2022) and all described as "Painful swelling of lymph nodes under arm & into breast tissue"; DIZZINESS (non-serious) with onset 14Jan2022, outcome "recovered" (15Jan2022), described as "Dizziness"; DIZZINESS (non-serious) with onset 14Jan2022, outcome "unknown", described as "Light-headedness when standing". Therapeutic measures were taken as a result of lymphadenopathy, lymph node pain. Therapeutic measures were not taken as a result of dizziness. Follow-Up (25Jan2022): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient's medical history: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Decreased appetite
Lethargy
Nasopharyngitis
Oropharyngeal pain
Pyrexia
Urticaria
Symptomtext
Low grade fever, with cold like symptoms (chills, lethargy, inappetence) within 24 hours of vaccination. 84 hours post vaccination, hives covering back, torso, and chest. 96 hours post hives spread to buttocks and thighs, sore throat and cold symptoms began as well no fever. At 1st symptom of hives, 25mg Benadryl taken and cold shower & air dry, repeated every 6-12 hours since. Benadryl and shower gives temporary relief, but no lasting improvement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- poly-cystic ovarian syndrom anemia anxiety disorder
- Andere Medikamente
- Sertraline 50mg PO SID Iron supplement 325mg PO SID NuvaRing vaginal birth control
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- -
- Beginn
- 04.02.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Urticaria
Urticaria chronic
Symptomtext
I developed hives after my Pfizer shots that progressed into chronic urticaria. It improved with antihistamine and recurred after my booster. However this time even worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Using anti histamine now
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Immediate post-injection reaction
Injection site erythema
Symptomtext
19 year old female patient in the observation area reports feeling dizzy. It is estimated alert in the 3 spheres. No respiratory distress, clear lungs, no itching and redness in the area of administration of the Pfizer FL3209 booster vaccine in the left upper extremity at 9:25am. Patient is evaluated at 9:55am and reports feeling dizzy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Cephalexin; Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Injection site pain
Pyrexia
Symptomtext
A 9-year-old girl came to the pharmacy on 2/4/2022 for 1st dose of the COVID-19 vaccine. We accidentally gave her COVID-19 vaccine for 12-year-old and above, instead of pediatric COVID-19 vaccine for 5 to 11-year-old. We notified the parent and MD, we gave the wrong vaccine. We will also follow-up with patient in a couple of days. Patient's parent claim she had soreness at injection site and low-grade fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Symptomtext
EXTREME CHILLS, HEADACHE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- AMLODIPINE TIZANDINE PROPRANOLOL
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Vision blurred
Symptomtext
A 17 year old female reported feeling blurred vision and dizziness after administration of the vaccine. Evaluation is preformed and S/V is taken. Consultation with Doctor is carried out, which indicates that she be placed on a stretcher and monitored for 30 minutes and her vitals are reassessed. After 30 minutes, the patients vitals are reassessed and she reports having improved her symptoms and feeling well. To which she withdraws from the center under her own feet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Fatigue
Nasal congestion
Sneezing
Symptomtext
So Basically right now I am very fatigue, It started out with nasal congestion, sneezing and a little cough, and those things have pretty much subsided and that started around the 22nd and now the only that I am really felling the is the fatigue and that has been going on since Jan 22, 2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic Lung Disease Hypertension Chlorestrol Eye Issues
- Andere Medikamente
- Vitamin C 1000 mg 1x daily Digestive Enzimes 4x daily 2 in the am & 2in the evening Iron 45mg 1x daily Zinc 45 mg 1x daily Vitamin B12 500 mcg 1x daily Fish Oil 1000 mg 1x daily Calicum 1200 mg 2x daily ProBiotic 13Billion 1x daily Ubiquino
- Allergien
- Sulfur Medications
- Vorherige Impfungen
- Techni Shot
- Staat
- VA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Fatigue
Headache
Injection site pain
Insomnia
Loss of personal independence in daily activities
Myalgia
Symptomtext
Left arm pain at injection site for a few days after the vaccine, plus headache and some fatigue. This was typical of my reaction after first two doses. Symptoms seems to resolve after a few days. After about a week, I noticed left arm pain in the area of the vaccination. This pain progressed over the next week from noticeable to severe the area of the injection site, area of my upper left arm to shoulder, and in left trapezius muscle. No numbness, weakness, tingling, or loss of strength in my left hand. Severe left arm, left shoulder pain/pain in left trapezius muscle was not resolved with Aleve at the maximum daily dose. As pain progressed, it interfered with daily activities and sleep. After two weeks the pain had not resolved and I went to urgent care. The urgent care doctor prescribed steroids for inflammation and muscle relaxers for the pain. I started taking the medication February 4, 2022. I intend to see my primary care doctor (listed as the primary POC for this issue) after the five day course of prednisone in the pain has not resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Rx for Prednisone 50 MG - 1 tablet 1x day for 5 days Rx for Methocarbamol 500 MG - 1 or 2 tablets every 8 hours as needed for pain
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Levothyroxine 150 mcg
- Allergien
- N/A
- Vorherige Impfungen
- As a child, vaccine doses were split due to sensitivity. As an adult, no vaccine reactions.
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Myalgia
Pyrexia
SARS-CoV-2 test
Symptomtext
Fever/ fever persisted for 14 days now; Muscle pain; Joint pain; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 46 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 08Jan2022 15:00 (Lot number: FL3209) at the age of 46 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EJ1685, Location of injection: Arm Left), administration date: 28Dec2020, when the patient was 45 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3302, Location of injection: Arm Left), administration date: 14Jan2021, when the patient was 45 years old, for Covid-19 immunization. The following information was reported: PYREXIA (medically significant) with onset 09Jan2022 06:00, outcome "not recovered", described as "Fever/ fever persisted for 14 days now"; MYALGIA (non-serious) with onset 09Jan2022 06:00, outcome "recovered", described as "Muscle pain"; ARTHRALGIA (non-serious) with onset 09Jan2022 06:00, outcome "recovered", described as "Joint pain". The events "fever/ fever persisted for 14 days now", "muscle pain" and "joint pain" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (21Jan2022) negative, notes: Nasal swab. Therapeutic measures were taken as a result of pyrexia, myalgia, arthralgia.; Sender's Comments: The event of Pyrexia is assessed as possibly related to the suspect drug bnt162b2 based on temporal association. 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
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220121; Test Name: RTPCR-Covid-19 Test; Test Result: Negative ; Comments: Nasal swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Chills
Ear pain
Insomnia
Pain in jaw
SARS-CoV-2 test
Vaccination site pain
Symptomtext
chills; pain in my jaw/behind the base of my left ear; upset stomach; trouble sleeping; soreness at injection site; pain in my jaw/behind the base of my left ear; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 40-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 11Jan2022 10:00 (Lot number: FL3209) at the age of 40 years as dose 3 (booster), single for covid-19 immunization. The patient had no relevant medical history. Concomitant medication(s) included: IBUPROFEN. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0182, Location of injection: Arm Left, Vaccine Administration Time: 01:00 PM), administration date: 08May2021, when the patient was 39 years old, for COVID-19 immunization, reaction(s): "No adverse event"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0161, Location of injection: Arm Left, Vaccine Administration Time: 08:00 PM), administration date: 17Apr2021, when the patient was 39 years old, for COVID-19 immunization, reaction(s): "No adverse event". The following information was reported: CHILLS (non-serious) with onset 11Jan2022, outcome "unknown", described as "chills"; EAR PAIN (non-serious), PAIN IN JAW (non-serious) all with onset 11Jan2022, outcome "unknown" and all described as "pain in my jaw/behind the base of my left ear"; ABDOMINAL DISCOMFORT (non-serious) with onset 11Jan2022, outcome "unknown", described as "upset stomach"; INSOMNIA (non-serious) with onset 11Jan2022, outcome "unknown", described as "trouble sleeping"; VACCINATION SITE PAIN (non-serious) with onset 11Jan2022, outcome "unknown", described as "soreness at injection site". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of chills, ear pain, abdominal discomfort, insomnia, vaccination site pain, pain in jaw. Additional information: The patient did not receive any other vaccine with in in four weeks of covid-19 vaccine. The patient was not diagnosed with Covid prior vaccination. The patient was tested for Covid post vaccination (iHealth Covid-19 Rapid Antigen Test (Nasal Swab) on 12Jan2022 resulted negative). The patient had no known allergies. The patient had some common Covid vaccine side effects, including chills, upset stomach, trouble sleeping, and soreness at injection site, so those weren't unexpected. But the one that seemed unusual was pain in jaw/behind the base of left ear. This pain was not constant, when it happened it was a stabbing pain that only lasted a moment each time. Sometimes it would happen once, and other times it happened many times in a row, with no pain or aches in between these brief stabbing pains. It was always in the exact same location. It happened off and on throughout the night, and mostly subsided the following day, other than happening a handful of times late the next morning. The patient never had anything like this happen before and was generally very healthy. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220112; Test Name: Covid-19 Rapid Antigen Test; Test Result: Negative ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- IBUPROFEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Rash
Symptomtext
Systemic: Allergic: Itch Generalized-Mild, Systemic: Allergic: Rash Generalized-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lymphadenopathy
Rash erythematous
Symptomtext
swollen tender R axillary with erythematous rash spreading to the R side of the chest with no pruritic, warmth, or pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- MOTRIN, OPERMAZOL
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Injection site pain
Pain
Urticaria
Symptomtext
Usual Right arm tenderness at injection site, tired, achy, and headache. But at 3pm, he developed hives most pronounced on arms and legs, but present on torso and back. He was given Benadrly 25mg and 1000mg Tylenol and went to bed at 10pm. When he awoke the next am at 6:30, all was resolved. He did NOT have any difficulty breathing, shortness of breath, trouble swallowing, lip or tongue edema.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Incorrect dose administered
Pain in extremity
Product preparation issue
Symptomtext
Clinician prepared vial with 1.3ml Normal Saline diluent rather than 1.8ml Normal Saline. Pt stated his arm hurt for 2 days after injection (denied redness/swelling) and had a headache. Stated symptoms resolved on own after 2 days. No other clinical concerns reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Pyrexia
Symptomtext
Patient has presented with headache, fever and tiredness. Patient's mother contacted daughter physician who recommended to give child acetaminophen and continue to observe. Child has an appointment on February 14, 2022 with pediatrician.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- not known
- Allergien
- not known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase normal
C-reactive protein
Decreased appetite
Differential white blood cell count normal
Dizziness
Dysstasia
Fatigue
Fibrin D dimer increased
Full blood count normal
Headache
Metabolic function test normal
Myalgia
Nausea
Neck pain
Pallor
Platelet count normal
Sensory disturbance
Symptomtext
Symptoms started the night of the shot and have persisted since. Didnt go to school at all last week. Feeling Dizzy, nausea, fatigue and feels like she cannot stand up sometimes. Appetite back to normal. Occ Headaches, pounding with some ringing. No h/o migraines. + Myalgias. No abdominal pain. No diarrhea. No chest pain + Neck pain today . Pallor. Took some curcumin and felt better. Pulse ox normal at home. Tried to go to school today but could only make it through half a day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- (CBC (INCLUDES DIFF/PLT)) (COMPREHENSIVE METABOLIC PANEL W/O eGFR) (HS CRP) (D-DIMER, QUANTITATIVE) Labs: All normal except following labs elevated ALT 22 D dimer 0.77
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NO
- Andere Medikamente
- NONE
- Allergien
- NO KNOWN DRUG ALLERGIES
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Pain
Pyrexia
Symptomtext
Fever, headache, body aches for >1 week
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Patient called the store around 6 PM complaining of hives after vaccine administration. Patient denied any signs of difficulty breathing or swelling of airway. Pharmacy manager counseled to administer Benadryl and report to nearest emergency room if symptoms continue to progress. Pharmacy manager attempted to call the next day to check in on the patient, but the patient was unavailable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Decreased appetite
Fatigue
Headache
Injection site bruising
Myalgia
Nausea
Tenderness
Symptomtext
Headache, muscle aches,chills, nausea, bruising at injection site. Also tenderness in armpit,shoulder blades, and pectorals. Loss of appetite and exhaustion. Symptoms lasted through 1/30/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 31.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
Musculoskeletal stiffness
Pyrexia
Symptomtext
Client reported two days after the vaccine he developed a fever. The client stated one week after the vaccine he developed a stiff neck and joint pain that lasted 3 days. The client stated he consulted with his friend who is a doctor who said the client, "almost had a stroke." The client was not formally diagnosed or prescribed any medications for his symptoms. The client denied any tingling, difficulty speaking, walking, or with facial movements. The client stated his friend who is a doctor recommended against receiving the 2nd COVID vaccine Pfizer. The client did not consult with his PCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Rash after taking Paracetamol.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 29.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Disturbance in attention
Headache
Pain
Rash erythematous
Symptomtext
Headache, inability to concentrate, and red rash approximately the size of a quarter over the injection site. Pain on left side of body from head to left foot. No pain on right side of body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Seasonal allergies to pollen.
- Andere Medikamente
- Zyrtec Allergy 10 mg, Equate Pain Reliever 500 mg.
- Allergien
- N/A
- Vorherige Impfungen
- Janssen COVID-19 Lot 18CSJ022, local Pharmacy, Age 24, vaccination date 03/18/2021. Severe body pain beginning about 12 hours af
- Staat
- -
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 29.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Nausea
Night sweats
Pain
Pyrexia
Vaccination site pain
Vomiting
Symptomtext
Fever; Chills; Nausea; Vomiting; Body aches; Injection site soreness for 6days+; Night sweats for a week+; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). A 27-year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in left arm, administration date 18Jan2022 (Lot number: FL3209) at the age of 27 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "None" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: EW0172; Route of administration: Intramuscular), administration date: 28Apr2021, when the patient was 26 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: ER8732; Route of administration: Intramuscular), administration date: 19May2021, when the patient was 26 years old, for COVID-19 immunisation. The following information was reported: PYREXIA (non-serious) with onset 19Jan2022, outcome "recovering", described as "Fever"; CHILLS (non-serious) with onset 19Jan2022, outcome "recovering", described as "Chills"; NAUSEA (non-serious) with onset 19Jan2022, outcome "recovering", described as "Nausea"; VOMITING (non-serious) with onset 19Jan2022, outcome "recovering", described as "Vomiting"; PAIN (non-serious) with onset 19Jan2022, outcome "recovering", described as "Body aches"; VACCINATION SITE PAIN (non-serious) with onset 19Jan2022, outcome "recovering", described as "Injection site soreness for 6days+"; NIGHT SWEATS (non-serious) with onset 19Jan2022, outcome "recovering", described as "Night sweats for a week+". Therapeutic measures were not taken as a result of pyrexia, chills, nausea, vomiting, pain, vaccination site pain and night sweats. Additional information: The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Dizziness
Headache
Nausea
Vomiting
Symptomtext
DIZZINESS, NAUSEA WITH VOMITING, HEADACHE, CHILLS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- hyperlipidemia, hypothyroidism, GERD
- Andere Medikamente
- Protonix, tirosint, lipitor
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 69,0
- Geschlecht
- U
- Eingang
- 27.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Immunisation
Lymphadenopathy
Nausea
Neck pain
Pain in extremity
Pain in jaw
Symptomtext
Full jaw, neck, shoulder and arm pain/ When eating or chewing food, pain would radiate from jaw and neck to shoulder and both arms; Full jaw, neck, shoulder and arm pain; Full jaw, neck, shoulder and arm pain; Arm pain/ When in store pushing carriage, arms would hurt to hold onto carriage while walking radiating to neck and shoulder; Swollen gland in left side of neck; Nausea 24h after vaccination; Dose received: 3; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 69-year-old patient received bnt162b2 (BNT162B2), administered in arm left, administration date 18Jan2022 at 14:00 (Lot number: FL3209) at the age of 69 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Arthritis" (unspecified if ongoing) and "Temporomandibular joint disorder" (unspecified if ongoing), notes: TMJ (mild flare ups). Concomitant medications included: VERAPAMIL; PREVACID; TOLTERODINE and ALEVE. Past drug history included: Compazine, reaction: "Drug allergy", notes: Known allergies: Compazine; Reglan, reaction: "Drug allergy", notes: Known allergies: Reglan and Tramadol, reaction: "Drug allergy", notes: Known allergies: Tramadol. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: Unknown; Administration location: Left arm; Route of administration: Unspecified), administration date: 01Apr2021, when the patient was 69 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: Unknown; Administration location: Left arm; Route of administration: Unspecified), administration date: 22Apr2021, when the patient was 69 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 18Jan2022 at 14:00, outcome "unknown", described as "Dose received: 3"; NAUSEA (non-serious) with onset 19Jan2022 at 14:00, outcome "not recovered", described as "Nausea 24h after vaccination"; PAIN IN JAW (non-serious) with onset 21Jan2022, outcome "not recovered", described as "Full jaw, neck, shoulder and arm pain/ When eating or chewing food, pain would radiate from jaw and neck to shoulder and both arms"; NECK PAIN (non-serious), ARTHRALGIA (non-serious), all with onset 21Jan2022, outcome "not recovered", and all described as "Full jaw, neck, shoulder and arm pain"; PAIN IN EXTREMITY (non-serious) with onset 21Jan2022, outcome "not recovered", described as "Arm pain/ When in store pushing carriage, arms would hurt to hold onto carriage while walking radiating to neck and shoulder"; LYMPHADENOPATHY (non-serious) with onset 21Jan2022, outcome "not recovered", described as "Swollen gland in left side of neck". Therapeutic measures were not taken as a result of nausea, pain in jaw, neck pain, arthralgia, pain in extremity and lymphadenopathy. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthritis; Temporomandibular joint disorder (TMJ (mild flare ups))
- Andere Medikamente
- VERAPAMIL; PREVACID; TOLTERODINE; ALEVE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Immunisation
Swelling
Symptomtext
Swelling and soreness in the left armpit; Swelling and soreness in the left armpit; booster dose; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 29 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 04Jan2022 18:30 (Lot number: FL3209) at the age of 29 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: If covid prior vaccination: Yes. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0173, Location of injection: Arm Left, Vaccine Administration Time: 09:30 AM), administration date: 12May2021, when the patient was 29 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0164, Location of injection: Arm Left, Vaccine Administration Time: 09:30 AM), administration date: 19Apr2021, when the patient was 29 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 04Jan2022 18:30, outcome "unknown", described as "booster dose"; SWELLING (non-serious), AXILLARY PAIN (non-serious) all with onset 06Jan2022 08:00, outcome "recovering" and all described as "Swelling and soreness in the left armpit". Therapeutic measures were not taken as a result of swelling, axillary pain. Additional information: There was no other vaccine in four weeks. No treatments for adverse events. Patient did not test covid post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (If covid prior vaccination: Yes).
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Client arrived at vaccination site. Client received hers first COVID vaccine (Pfizer on 01/05/22 lot: FL3209 exp: unknown). Per Client, "2 days after my first dose I started noticing that I developed some rashes on my neck, both arms and my inner thighs down to my knees. I still have a little bit on my inner thighs, but the rest are gone." Client reported that she did not use any new products on her skin before or after her first dose and that she did not report this rash to her Primary Care Physician. Client requested to receive her second Pfizer COVID vaccine. Client reported that she has no chronic medical conditions, she is currently not taking any medications and has no known allergies. RN, submitted a medical consult via text to Vaccine Operations and approval via text from Dr. was obtained for client to receive second the Pfizer COVID vaccine. RN educated client on ER precautions and when to follow up with her Primary Care Physician and recommended for client to see her Physician about her rash. Client verbalized understanding. Client received her second Pfizer COVID vaccine lot: FK9896 exp: 06/30/22. Client completed 30 minutes observation with no adverse reactions and left facility at 11:15 AM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- No chronic medical conditions
- Andere Medikamente
- No medications
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Body temperature increased
Burning sensation
Headache
Insomnia
Symptomtext
That night she begin to have severe headache. She felt as if she was on fire and she believe her head was melting. Later that night around 10PM, she had a temperature of 102.9. She was not able to sleep because of her head was hurting really bad. That falling Monday she was still experiencing headaches and still not able to sleep. I took her to nearest emergency room.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Chronic Hives; Brain issue; ADHD
- Andere Medikamente
- None
- Allergien
- Benadryl
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fatigue
Immediate post-injection reaction
Injection site rash
Laboratory test
Pain in extremity
Symptomtext
Immediately following adminstration (within seconds), I felt lightheaded and completely enervated. This lasted a good twenty minutes I believe (you can check with my doctor?s notes). Because I had had a reaction to Pfizer first dose, my allergist was giving me the booster in her clinic. She split th e dose in half. At 17 minutes post first half-dose, my doctor had me take a Claritin pill. That did the trick; at 30 min, the lightheaded was gone and only the tiredness remained. So my doctor?s nurse administered second half-dose?I did not get light-headed. The extreme tiredness lasted through the following day. Day 2 post-booster I got a rash at the injection site (also sore arm but everyone gets that). Rash lasted a day; I used 2.5% hydrocortisone cream to calm it down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- My doctor sent me for MCAS testing during the event (on 1/13/22) to see if I was having a mast cell reaction. She has not yet provided me with those test results.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Severe osteoporosis
- Andere Medikamente
- Pepcid, Allegra Vitamins B, C, D, Calcium, fish oil.
- Allergien
- Latex, bee stings. One previous anaphylaxis, cause unknown, eight years ago.
- Vorherige Impfungen
- Dizziness lasting on/off for eight hours immediately following administration of Pfizer first dose, on 4/8/21.
- Staat
- PR
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Fatigue
Pyrexia
Symptomtext
Dizziness, Chills, Fever and tiredness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Epilepsy
- Vorgeschichte
- -
- Andere Medikamente
- Lamictal 100mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Fatigue
Headache
Vomiting
Symptomtext
Has been vomiting, headaches, exhausted, and light headed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Same as this event to 2nd Pfizer shot.
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Back pain
Rash
Rash erythematous
SARS-CoV-2 test negative
Throat tightness
Symptomtext
Started with tight throat , then a red rash appeared on face . Had to start Zyrtec . Now have immense stomach pain and back pain . Have taken several Covid tests at testing location , all negative
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Will need to do lab work to see what is happening
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi vitamin
- Allergien
- Benzoyl peroxide
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site pain
Injection site pruritus
Injection site swelling
Pruritus
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Allergic: Itch Generalized-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Eye swelling
Headache
Lymphadenopathy
Symptomtext
Began 10 hours after his vaccination he began to experience chills. 24 hours after his vaccination he had serious swelling in his left eye. Headaches and additional swelling under his left arm pit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Has experienced several random headaches a month leading up to vaccination.
- Vorgeschichte
- N/A
- Andere Medikamente
- Nyquil on the night of reaction at 2300.
- Allergien
- PCN.
- Vorherige Impfungen
- Pfizer (2nd dose) ER8736 Experienced headaches for two weeks date(04/21/21)
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Pyrexia
SARS-CoV-2 test
Symptomtext
chills, fever, joint pain x 1 week
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- covid 1/25/2022 - pending results
- Aktuelle Erkrankungen
- Shingrix
- Vorgeschichte
- DM, HTN, HLD
- Andere Medikamente
- metformin Tylenol hydroxyzine
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nausea
Pyrexia
Symptomtext
Fever >101? beginning approx 24 hours after injection. Fever gone with 200-400mg Ibuprofen. Fever would recur approx 6-10 hours later, lasting 48 hours. Nausea also.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mild asthma, gerd, seasonal allergies
- Andere Medikamente
- OMEPRAZOLE DR 20 MG, MONTELUKAST SOD 10 MG, Claritin, 500 mg calcium, 2000IU Vitamin D3
- Allergien
- Seasonal allergies treated with allergy shots
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Injection site induration
Injection site nodule
Pruritus
Symptomtext
large hard bump (knot-like) on injection site, very itchy and red
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site induration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- thyroid
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Erythema
Hyperhidrosis
Pallor
Pruritus
Visual impairment
Symptomtext
Client reported feeling dizzy to RN. Client ambulated and sat down in the anti-gravity chair. RN adjusted the anti-gravity chair to a low fowler's position. RN responded. The following was obtained with RN translating between Spanish and English. RN noted pallor of the client's face and diaphoresis on the client's face. The client reported seeing white spots and dizziness. Vitals obtained at 02:56PM were as follows: automatic BP 97/46, HR 68, O2 97%. The client state she last ate at 2:00 PM. The client denied any chronic conditions or known allergies. The client reported a history of fainting twice before once when she exercised too hard and another after seeing blood. The client stated she experienced vision changes with the two previous episodes of syncope. The client received the first dose of COVID vaccine Janssen on 06/22/21 and denied any adverse reaction. Vitals obtained at 02:59PM were as follows: manual BP 94/50, HR 71, O2 99%. The client denied any other s/s of anaphylaxis. The anti-gravity chair was adjusted to a high-fowler's position. The client reported mild persistent dizziness. RN noted decrease in pallor on the client's face. Vitals obtained at 03:04PM were as follows: manual BP 102/56, HR 87, O2 99%. The client denied any current symptoms. The client began drinking a juice and eating animal crackers. Vitals obtained at 03:09PM were as follows: manual BP 102/58, HR 72, O2 99%. The client denied any current symptoms. The client's boyfriend joined the client next to the anti-gravity chair. Vitals obtained at 03:19PM were as follows: manual BP 114/68, HR 68, O2 98%. The client reported itchiness on the left side of her neck and on the right side of her scalp. RN noted a red spot about one inch in diameter on the left side of the client's neck. The client stated she had scratched the spot. RN noted no visible redness on the client's scalp where the client pointed the itchiness was located. RN noted no redness around the vaccination site or the client's right arm. Mild pink discoloration was located on the client's forearm. The client denied any itching on her arm. RN offered the client Benadryl and educated on the possible adverse effects. The client declined the Benadryl stating that she was riding a motorcycle home. The client then stated the itching resolved. RN noted a decrease in size and discoloration of the redness of the spot on the client's neck. RN provided education regarding possible adverse events and when to seek care. The client voiced understanding of this education. Repeat vitals obtained at 3:27PM were as follows: BP 110/62, HR 98%, O2 98%. The client denied any current symptoms. The client ambulated unassisted with a steady gait out of the vaccination site at 3:34PM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Nausea
Pyrexia
Symptomtext
Fatigue, nausea, fever (103.2). Treated with Advil and rest. Symptoms moderated with this but not eliminated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- MMR vaccine, intramuscular, approx 9 months old, fever of 103+
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Dizziness
Dry throat
Headache
Pain in extremity
Symptomtext
Weakness, chills, dizziness, dry throat, headache, severe arm pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chromaturia
Immunisation
Pain
Pyrexia
Symptomtext
noticed a darkened urine color and still its happening; Fever & Body pain - almost gone; Fever & Body pain - almost gone; dose number 3; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 32 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 05Jan2022 18:45 (Lot number: FL3209) at the age of 32 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0182, Location of injection: Arm Left, Vaccine Administration Time: 01:00 PM), administration date: 07May2021, when the patient was 32 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0161, Location of injection: Arm Left, Vaccine Administration Time: 01:15 PM), administration date: 16Apr2021, when the patient was 32 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 05Jan2022 18:45, outcome "unknown", described as "dose number 3"; CHROMATURIA (non-serious) with onset 05Jan2022 19:15, outcome "not recovered", described as "noticed a darkened urine color and still its happening"; PYREXIA (non-serious), PAIN (non-serious) all with onset 05Jan2022 19:15, outcome "recovering" and all described as "Fever & Body pain - almost gone". Therapeutic measures were not taken as a result of chromaturia. Therapeutic measures were taken as a result of pyrexia, pain. Additional information: Facility where the most recent COVID-19 vaccine administered was Pharmacy or Drug Store. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that the patient was getting following side effects or events after 3rd COVID-19 Vaccine Pfizer BioNTech. The patient noticed a darkened urine color and it still was happening. The patient had fever and body pain - almost gone. The patient took 2 times Tylenol. The patient had no other medical issue and no known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History:Patient Other Relevant History 1: None, Comment: known allergies: No. Other Medical History: No.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Headache
Pain
Pyrexia
Symptomtext
104 F. fever, body aches, headaches, and coughing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Sneezing/Coughing/Runny Nose
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Contusion
Lymphadenopathy
Swelling
Vomiting
Symptomtext
On 1/18/22 swelling started in the morning up to the neck and lymph nodes. On 1/19/2022 bruising and vomiting started in the evening. On 1/20/2022 mom took her to the urgent care in the morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- Not reported.
- Aktuelle Erkrankungen
- Not reported
- Vorgeschichte
- Not reported
- Andere Medikamente
- Not reported
- Allergien
- Not reported
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Hyperhidrosis
Pyrexia
Symptomtext
Uncontrolled shivering, fever 103.7 deg; sweats; lasted 8 hrs until fever broke; started 10 hrs after injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Type 1 Diabetes (insulin admin. by pump);
- Andere Medikamente
- regular insulin; Ramipril; Lunesta 3 mg; 81 mg aspirin; vitamin D3; Zinc;
- Allergien
- Codeine
- Vorherige Impfungen
- 01-28-2021; Pfizer; intramuscular; 1st dose; 68 yo
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Axillary pain
Symptomtext
I got the vaccine on my left arm, and a lump appeared on my left arm pit and it hurt. My arm pit got swollen, but it's slowly going away. This was for the 3rd dose of pfizer for the other 2 I didn't have any reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Thyroid medication, Levithorixide and birth control Junel Fe lowest dose
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Symptomtext
Site: Bruising at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Chest discomfort
Heart rate increased
Swelling
Symptomtext
Previously received Moderna vaccine on 3/16/21 and 4/13/21. This was the first Pfizer vaccine that I received. Received vaccine at 10am on 1/17/22. Around noon on 1/18/22, noticed tightness in chest. Checked heart rate and resting heart rate wouldn't go below 110 (normally in the 70s for me). Continued like this until roughly 8pm, where it stayed in the 80s throughout the night. Also during the night I noticed armpit pain and woke up 1/19/22 to swelling of my right armpit. As of 5pm, the pain is nearly gone but the swelling has remained. While I actually felt better with this vaccine than with my last Moderna vaccine, these symptoms were new to me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Tested positive for COVID around December 10th. Got flu vaccine in early January.
- Vorgeschichte
- -
- Andere Medikamente
- Pantoprazole, Linzess, Bupropion, Amitriptyline, ALLEGRA
- Allergien
- Penicillin, Flagyl
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site pain
Injection site swelling
Symptomtext
Site: Bruising at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Swelling at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dizziness
Eye disorder
Nausea
Visual impairment
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Nausea-Mild, Systemic: Weakness-Mild, Additional Details: Patient was having eye/visual complaint before administering Pfizer vaccine. After administering Pfizer vaccine, patient stated she feels dizzy, nauseated, and weakness. Followed protocol, monitoring patient, advised district leader, and called 911
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Symptomtext
Whole body itching for 7 days (arms, hands, legs, torso and pelvis).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Daily probiotics
- Allergien
- Fish allergy
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Headache
Symptomtext
After 5-10 minutes of injection, patient complained of headaches and chest tightness. Blood pressure was measured, sbp 160. Patient refused 911 call. After deep breathing and drinking water, patient felt better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- No allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Headache
Influenza like illness
Muscle tightness
Neck pain
Pain
Symptomtext
I was feeling great the morning I got it. Next day flu like symptoms. Didn't feel quite right for the next 4-5 days. Then I got an extreme headache on day 7, day 9 extreme muscle tightness all over, especially in the head area and I felt like I just got off a boat. I didn't have vertigo but my balance which is usually so strong was totally off. Starting to feel a little bit better. Went to my doctor and got a steroid shot but hoping I will start to feel like myself again soon. I am angry right now that I got it. Stop lying to us.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Saw my chiropractor for adjustment and decompression therapy on 1/12 and 1/15 due to sore neck and body. Saw my internist on 1/15 for anti inflammatory for muscle tightness and finally went to my ENT today thinking I had a sinus issue due to being off balanced. He gave me a steroid shot and informed me that I was among several of his patients with the same complaint after receiving the booster.
- Aktuelle Erkrankungen
- none felt great
- Vorgeschichte
- hasimotos thyroid disease
- Andere Medikamente
- synthyroid 150 mcg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Activated partial thromboplastin time normal
Acute kidney injury
Alanine aminotransferase normal
Anion gap
Antinuclear antibody negative
Aspartate aminotransferase normal
Back pain
Bacterial test negative
Basophil count decreased
Basophil percentage
Bilirubin conjugated normal
Bilirubin urine
Blood albumin decreased
Blood alkaline phosphatase decreased
Blood alkaline phosphatase increased
Blood bilirubin normal
Blood bilirubin unconjugated normal
Blood calcium decreased
Symptomtext
The patient received his vaccination on 1/13/2022 at 4pm. During the early morning of 1/14/2022 he developed severe muscle pain especially in the bilateral costovertebral angles, fever, and severe headache. Upon arising later that morning he had dysuria and gross hematuria without clots along with the aforementioned symptoms. Seen in the emergency department at Medical Center on January 14th. Noted to have acute kidney injury with creatinine of 1.1 mg/dl, gross hematuria, normal C3 & C4, normal CBC including normal platelet count. Normal INR and APTT. Urine grossly reddish brown in appearance with >100 RBC/HPF. Urine protein/creatinine ratio is 0.882. BP was134/72 mmHg. Urine culture was sterile from that day. Re-evaluated on 1/17/2022. BP was within normal range for age at 110/78 mmHg. Clinically free of edema. Still with backpain that is remarkably tender and dysuria. Compliant of severe headache. His laboratory studies show a creatinine of 1.2 mg/dl. Urinalysis with RBC and coarse granular casts. Urine protein/creatinine ratio improved to 0.352
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- 1/17/22 12:27Complement, C-4 Performing Facility: Labs C-4 31.7 1/17/22 12:27Complement, C-3 Performing Facility: Labs, C-3 104 C-3:No reference range established for this age group. 1/17/22 12:27Automated Chemistry Performing Facility: Labs, TP-Pla 6.3 LAlbumin 3.8 LT-Bili 0.3AST 20T-Alkp 239Na 140K 4.7Cl 106CO2 30A-Gap 4Urea N 11Creat 1.2Gluc 97Ca 8.7ALT 14eGFR N/A eGFR:GFR is not calculated on patient under the age of 18 1/17/22 12:27CK - Creatine Kinase Performing Facility: Labs, CK 105 CK:Outpatient CK reference ranges vary considerably with physical activity and range up to 320 U/L for males and 230 U/L for females. 1/17/22 11:40Urine, Microscopic Only URINE Performing Facility: Labs, Hyl 0-2R-Epi None SeenWBC 6-10RBC >100 AR-Epi None SeenSquam 0-2Mucus None SeenBacti None SeenAmorph None SeenCryst None SeenGran None Seen 1/17/22 11:40Protein-Creat Ratio URINE Performing Facility: Labs, Pro-RU 34.8Cre-RU 98.8Pro/Cr 0.352 H Pro-RU: No reference range for this analyte/specimen type. Cre-RU: No reference range established. 1/17/22 11:40Urine, Dipstick & Micro URINE Performing Facility: Labs, Color YellowTurb 2+ ASp-Gr 1.013pH 7.0Prot 30 AGluc NEGKeto NEGBili NEGBld 3+ AUro NormEster NEGNitr NEG 1/15/22 02:32Complement, C-4 Performing Facility: Labs, C-4 25.9 1/15/22 02:32Complement, C-3 Performing Facility: Labs, C-3 92 C-3:No reference range established for this age group. 1/15/22 02:32Double Stranded DNA Abs Performing Facility: Labs, dsDNA Ab 2 dsDNA Ab:<= 4 IU/mL negative for dsDNA antibodies5 - 9 IU/mL indeterminate for dsDNA antibodies>= 10 IU/mL positive for dsDNA antibodies 1/15/22 02:32ANA Immunofluorescent (HEp2) Performing Facility: Labs, ANA(HEp-2) NEG <1:80Interp ANA No interpretation 1/15/22 02:32Protein-Creat Ratio URINE Performing Facility: Labs, Pro-RU 107.8Cre-RU 122.2Pro/Cr 0.882 H Pro-RU: No reference range for this analyte/specimen type. Cre-RU: No reference range established. 1/15/22 02:32Streptococcal Ab-ASO only Performing Facility: Labs, ASO 367 ASO:No reference range established for this age group. 1/15/22 01:37Troponin I 2 Hour Performing Facility: Labs, Troponin I, HS 2Hr <3 Troponin I, HS 2Hr: Ordered secondary to Hs Troponin I (Serial) order. 1/14/22 23:52Troponin I 0 Hour Performing Facility: Labs, Troponin I, HS 4 1/14/22 23:52CK - Creatine Kinase Performing Facility: Labs, CK 249 H CK:Outpatient CK reference ranges vary considerably with physical activity and range up to 320 U/L for males and 230 U/L for females. 1/14/22 23:52C-Reactive Protein Performing Facility: Labs, C-Reac-Prot 2.5 H 1/14/22 23:33Automated Chemistry Performing Facility: Labs, TP-Pla 6.9Albumin 4.0T-Bili 0.4D-Bili 0.1I-Bili 0.3AST 28T-Alkp 282ALT 19 1/14/22 23:33Prothrombin Time-INR Performing Facility: Labs, INR 1.1 1/14/22 23:33Culture, Urine-Id Org & Sensi URINE, CLEAN CATCH 1/16/22 Performing Facility: Labs, . No Growth (<1,000 cfu/ml) 1/14/22 23:33APTT - Part. Thrombo Time Performing Facility: Labs, APTT 29.9 1/14/22 23:33Urine, Microscopic Only URINE Performing Facility: Labs, Hyl None SeenR-Epi None SeenWBC 3-5RBC >100 AR-Epi None SeenSquam None SeenMucus None SeenBacti TraceAmorph 1+Cryst None SeenGran None Seen 1/14/22 23:33Automated Differential Performing Facility: Labs, Lymph 28Mono 14Lymph# 1.5Mono# 0.7Eos# 0.1Baso# 0.0Neut 56Eos 1Baso 1IANC# 2.9 1/14/22 23:33Automated Chemistry Performing Facility: Labs, Na 139K 3.9Cl 105CO2 28A-Gap 6Urea N 17Creat 1.1Gluc 105 HCa 8.6eGFR N/A eGFR:GFR is not calculated on patient under the age of 18 1/14/22 23:33CBC with Auto Diff Performing Facility: Labs, WBC 5.2RBC 4.35Hgb 13.5Hct 39.7MCV 91.3MCH 31.1MCHC 34.1RDW 13.0Plt 260MPV 7.4 1/14/22 23:33Urine, Dipstick & Micro URINE Performing Facility: Labs, Color Brown ATurb 3+ ASp-Gr 1.025pH 6.5Prot >=300 AGluc 100 AKeto 1+ ABili NEGBld 3+ AUro Elev AEster 1+ ANitr POS A 1/14/22 00:03Lactate, Venous, 0Hr, Sepsis Performing Facility: Labs, Lact-Ven 0.7 HISTORY: Flank pain, hematuria COMPARISON: None Provided. FINDINGS: No acute cardiopulmonary pathology is seen at the lung bases. Please note that absence of intravenous contrast limits evaluation for solid organ/vascular pathology and anatomy. The unenhanced liver demonstrates no gross acute abnormality. The gallbladder is grossly unremarkable. There is no evidence of biliary ductal dilatation. The spleen demonstrates no gross acute abnormality. The pancreas demonstrates no gross acute abnormality. No acute findings are seen in the adrenal glands. No gross acute findings are seen in the unenhanced kidneys. No obstructive renal, ureteral, or bladder calculi are seen. There is no evidence of bowel obstruction or perforation. The appendix is grossly unremarkable. No acute skeletal pathology is seen. IMPRESSION: No obstructive uropathy. No gross acute abdominopelvic pathology on this unenhanced study. ELECTRONICALLY SIGNED BY: , MD Jan 15, 2022 1:04:04 AM CST This report is intended for review by the ordering physician only, in accordance of law. If you receive this report in error, please call Radiology at (redacted). The above is a preliminary report. The final report will appear below once the final interpretation is completed. Final Impression I have reviewed the study and the preliminary report and agree
- Aktuelle Erkrankungen
- None Had COVID in November 2021
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Axillary pain
Breast pain
Breast swelling
Chills
Erythema
Headache
Pain
Pyrexia
Swelling
Symptomtext
Headache, Pain, swelling and redness in arm for a week. Chills, upset stomach, fever for 2days. On day 3 pain in armpit that spread down my side and eventually into my breast along with swelling and redness. Everything finally subsided after day 7 of vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Ulcerative Colitis Migraines Hypothyroidism High Cholesterol
- Andere Medikamente
- Alive womens vitamin Mesalamine Amitriptyline Levothyroxine Simvastatin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Injection site haematoma
Injection site rash
Injection site swelling
Symptomtext
During administration a vessel was hit and patient had immediate swelling at site and a hematoma formed and she returned with a rash and swelling at the site. I had her apply an ice pack for 10 minutes and looked at site the swelling had lessened but still bumpy rash and hematoma. Discussed with her if she felt any more symptoms to seek medical advice.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site haematoma
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- nothing
- Andere Medikamente
- unknown
- Allergien
- none listed
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Incorrect product formulation administered
Symptomtext
Administered 0.3ml dose of undiluted vaccine. Mild symptom of chills approximately 24 hours after administration treated with ibuprofen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Nausea
Symptomtext
Dizziness and nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Codeine. Red dye.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary mass
Axillary pain
Immunisation
Symptomtext
The day following my booster shot, I got a very tender sometimes painful swollen lump under my right arm. Located where the chest and axilla meet.; The day following my booster shot, I got a very tender sometimes painful swollen lump under my right arm. Located where the chest and axilla meet.; Dose number 3; This is a spontaneous report received from a non-contactable reporter (consumer or other non-HCP). The reporter is the patient. An adult female patient (not pregnant) received bnt162b2 (BNT162B2), administered in right arm, administration date 05Jan2022 at 16:00 (Lot number: FL3209) as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history was not reported. Patient did not receive any concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: EM9809, Route of Administration: unspecified), for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: ER2613, Route of Administration: unspecified), for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 05Jan2022 at 16:00, outcome "unknown", described as "Dose number 3"; AXILLARY MASS (non-serious), AXILLARY PAIN (non-serious) all with onset 06Jan2022, outcome "recovered" (10Jan2022), and all described as "The day following my booster shot, I got a very tender sometimes painful swollen lump under my right arm. Located where the chest and axilla meet". Therapeutic measures were not taken as a result of axillary mass and axillary pain. Additional Information: Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. It was reported that the tender swelling remained for 4 days. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Malaise
Retching
Vomiting
Symptomtext
Patient woke up the next day, after sleeping late. He complained he didn't feel well. He went to a storage unit with his older sister to help load boxes into her car. They had to stop and rush home. He vomited liquids until clear several times. Then he dry heaved. Afterwards, he took 2 Ibuprofin, a total dose of 400mg. He went to bed the rest of the day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- fever and screaming later in the evening, age <1 year old, before 3/2007
- Staat
- OH
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Cough
Fatigue
Headache
Lymphadenopathy
Malaise
Musculoskeletal stiffness
Nausea
Rhinorrhoea
SARS-CoV-2 test
Symptomtext
Swollen under arm lymph nodes, headache, cough, runny nose, stiff neck, nausea, join pain, fatigue, and malaise.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- COVID-19 swab test performed on 1-11-2022. Results not available yet.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes, Sleep Apnea, PCOS, Fibromyalgia, Migraines, IBS, Degenerative Disk Disease
- Andere Medikamente
- metFORMIN ER 750 mg 24 hr tablet, cetirizine 10 mg tablet, propranolol 20 mg tablet, norgestimate 0.25 mg-ethinyl estradiol 35 mcg 0.25-35 mg-mcg per tablet, escitalopram oxalate 20 mg tablet, buPROPion XL 150 mg 24 hr tablet, Centrum Women
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Lymph node pain
Lymphadenopathy
Pain
Symptomtext
I WOKE UP & HAD BODY ACHES & CHILLS & ALL OF MY LYMPHNODES UNDER MY LEFT ARMPIT & MY BREAST WERE SWOLLEN & VERY PAINFUL I COULDNT KEEP MY ARM DOWN AT MY SIDES I HAD TO HOLD MY ARM & SHOULDER IN POSITION AS IF I HAD ON A SLING I WAITED 2 DAYS TO GO TO URGENT CARE BUT COULD NOT GET APPT SO I WAITED 2 MORE DAYS & THEN I GOT TELEHEALTH APPT & WAS TOLD TO USE HEATING PAD & TAKE TYLENOL & IBUFPROFEN & SYMPTOMS STARTED TO DECLINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- ASTHMA
- Andere Medikamente
- ZYRTEC, CITALOPRAM
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Dizziness postural
Feeling hot
Symptomtext
pop up clinic at local meat packing plant. patient c/o of feeling Hot, dizzy 10-15 minutes post injection. unable to stand without dizziness. actions taken - cold compress, feet elevated, water 12-16 oz, juice 12 once. patient continued to c/o dizziness . 911 called by staff at 1030 - BP 168/90, pulse 98
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unk
- Vorgeschichte
- unk
- Andere Medikamente
- unk
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pruritus
Urticaria
Symptomtext
Patient reported itching to site post vaccination. Onset of 10 minutes post vaccine. Noted spreading urticaria to left arm adjacent to site of administration. Patient denies airway involvement. No respiratory distress noted, patient speaking in full sentences. VS as follow BP 132/74 HR 77 Oxygen saturation 95% on RA 16 RR. MD Stat called. Dr. and RN responded to assess patient. After assessment MD decided to take patient to clinic. Patient ambulated out of the vaccine clinic with a strong and steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- NA
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Urticaria started 2 days after vaccination. Started on abdomen and spread to face. Worsened x 2 days. Provided antihistamine treatments.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Celiac disease, asthma, eczema
- Andere Medikamente
- None
- Allergien
- Gluten, Chocolate, citrus
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Asthenia
Fatigue
Headache
Myalgia
Nausea
Vomiting
Symptomtext
Severe fatigue, nausea, headache, all joints ached, all muscles ached, vomiting, weakness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- nothing
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chills
Headache
Lymphadenopathy
Symptomtext
chills, R axillary lymphadenopathy, head ache (as expected), mild chest discomfort that is reproducible with inhalation and movement
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- exam and vitals, referred to PCP for follow up, EKG/echo not available at the minute clinic
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- anxiety, fibromyalgia, htn,
- Andere Medikamente
- Vitamin D3, celexa, apri, gabapentin, spirolactone
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Tension headache
Symptomtext
21yo F patient with no PMH, here to receive the Pfizer COVID vaccine booster. Immediately after receiving the vaccine she felt her "head was tense". Patient is associating the event to the fact that she was very anxious and scare about the vaccine. With the primary 2 doses she had lightheadedness that self-resolved within minutes. Denied any other symptom. Patient was evaluated by on-site EMS and MD. On PE AAO x 3; Initial VS: HR 77, RR 18, SpO2 100%, BP 110/60. Heart with RRR, lungs clear bilaterally. Patient was offered water and juice. After 15min observation patient felt better, repeated set of VS within normal limits. Patient was discharged with complete resolution of symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tension headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Impaired driving ability
Impaired work ability
Symptomtext
Dizziness. Unresolved at this time. Unable to work or drive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None at this time.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, Allergies
- Andere Medikamente
- Zinc, vitamin C, Zyrtec, Progesterone
- Allergien
- Codeine, Bactrim
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 09.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Pallor
Pyrexia
Symptomtext
Patient received third dose (0.3 mL) of Pfizer Covid vaccine. Promptly after vaccination, patient's spouse reported patient had increased sweating, pale face, feeling of lightheadedness, and low-grade fever. Patient was instructed to sit, patient's temperature returned to normal to 96.1 F after several minutes. Pharmacy offered to call 9-1-1 for emergency services at time of event and patient declined. Patient received water while sitting. Patient returned to baseline after ~15 minutes with no sweating, normal face color and no feeling of lightheadedness. Patient was monitored throughout the event and patient indicated he felt stable and wished to return home after ~15 minutes of monitoring.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- No chronic health conditions reported
- Andere Medikamente
- None
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 09.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Pain
Pain in extremity
Peripheral swelling
Pyrexia
Symptomtext
High fever (103) one day after vaccination but more concerning is that the arm swelled up, not at the injection site but lower in the arm in the posterior upper arm area. Also, severe pain under left arm and very swollen lymph nodes requiring Motrin to alleviate the pain. He also reported a bad pain shooting down the arm at the time of injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None at this time. Vaccine was only 2 days ago.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Multivitamin once daily
- Allergien
- Cats
- Vorherige Impfungen
- Pfizer dose 2
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Client C/O dizziness. Writer called on NP, Site Lead and EMS. Client stood up and walked into the clinical setting, escorted by EMS and writer. Staff lowered client to the floor on a mat, inside of the clinical setting. Ortho B/P's along with O2 saturation and pulse obtained. Initial V/S @1132 noted as 107/68, 96% O2 on RA and P 83. During assessment, client and her mother verbally explained that client has a HX of anxiety during blood draws. Clients 1142 V/S completed in a laying position, noted as 105/65, P 85 and O2 98%; @1152 V/S completed in a sitting position as 101/67, O2 100% on RA, P 85; V/S completed @ 1203 in a standing position noted as B/P 103/71, P 89 and O2 100% on RA. Client monitored for an additional 15 minutes in the outside monitoring area before being discharged by NP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Client verbalized post incident origination that she has a HX of anxiety r/t blood work. No other pre existing conditions noted or verbalized.
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye swelling
Injection site pain
Lymphadenopathy
Symptomtext
Pain at injection site, swollen lymph nodes under left arm, swollen right eye
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Cantaloupe allergy
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Fatigue
Hyperhidrosis
Myalgia
Nausea
Symptomtext
Extreme fatigue, sweating profusely, chills, mild nausea, weakness, muscle pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression, anxiety, low back pain
- Andere Medikamente
- Viibryd, Wellbutrin, vitamin D, multivitamin, vitamin C, Allegra
- Allergien
- Penicillin, lobster, pollens, dust, dander
- Vorherige Impfungen
- Allergic reaction to Flu shot causing throat to swell, 2003, age 21,
- Staat
- PR
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Rash erythematous
Rash pruritic
Urticaria
Symptomtext
Urticarial rash that started within the first five hours of receiving the booster. Described as an itchy erythematous rash, like hives, that started in the back and spread to arms and legs the following day. Received treatment with Bendadryl and Zyrtec without improvement of symptoms. No previous similar episodes with other vaccines or medications. Patient with No known allergy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Before receiving vaccine, patient emphasized verbally that she has had a history of vasovagal reaction to vaccines. Parents were accompanying her. Patient received vaccine at approximately 1:25pm. Patient did not immediately feel faint after the vaccination, and then stepped out to have a seat at the pharmacy waiting area. Patient started to feel faint at approximately 1:30pm. Parents called for a pharmacist and proceeded to elevate her feet and have her lie down on the floor. I asked if patient was feeling any other symptoms, such as chest pain, difficulty breathing, etc. Patient denied feeling any other symptoms other than lightheadedness. I offered to call for an ambulance, but patient and parents denied to call for ambulance. Asked patient and parents to remain in the waiting area for at least another 15 minutes. Patient reported feeling better at approximate 2:08pm before leaving. I advised them to seek immediate medical care if any new symptoms start to develop, especially if there was any chest pain, any new fainting, difficulty breathing, etc. I also advised them to make sure to follow up with the primary medical provider
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- penicillin
- Vorherige Impfungen
- any vaccine, per patient
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Nausea
Pain
Pyrexia
Rhinorrhoea
Symptomtext
Fever of up to 101.4, chills, body aches, nausea, runny nose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Zinc, vitamin D, Iron, fish oil
- Allergien
- -
- Vorherige Impfungen
- Pfizer Covid vaccine 2nd dose
- Staat
- PR
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Headache
Pain
Pain in extremity
Peripheral coldness
Symptomtext
Strong pain in the whole arm up to the fingertips Cold hand Strong pain in the armpit radiating to the breast. Headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Hypothyroidism; Cardiac
- Vorgeschichte
- Cervical stenosis; Anxiety
- Andere Medikamente
- Synthroid 25 mcg
- Allergien
- Fentanyl
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deafness unilateral
Ear pain
Lymph node pain
Lymphadenopathy
Otitis media
Otorrhoea
Pain
Tinnitus
Symptomtext
Enlarged and swollen left supraclavicular lymph node that was tender and painful to the touch. Started a few hours after vaccine administration for 1 week and has mostly resolved itself. Intense left ear pain radiating into left jaw, hearing loss and tinnitus in left ear, yellow discharge coming from left ear. Started 2-3 days after vaccine administration. Diagnosed with left ear otitis media ear infection. Pain has improved substantially after day 4 treated with oral Amoxicillin, ibuprofen, Tylenol, and Sudafed. Other symptoms improving but not resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COVID-19 infection (positive test) on November 29, 2021 (one month prior to booster).
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Azithromycin.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Symptomtext
3:30: The patient felt faint and appeared diaphoretic, blood pressure taken pt remained in sitting position AOx3. B/P 96/60, HR 65 02 sat 99%. 3;35 Patient remained in sitting position no c/o nausea. 3:50 Pt states feeling better is with Mother, encouraged to follow up with primary MD if symptoms return. final B/P 108/64, left with mother
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Headache
Lymphadenopathy
Symptomtext
Headaches, chills, and swollen armpit lymph node in injection arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Symptomtext
patient became itchy all over approximately 15 minutes after shot administered gave her a 50mg dose of benadryl pt reported feeling much better 1 hour later
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- hbp
- Andere Medikamente
- lisinopril 5mg, vit d3 50,000 units qw , breo inhaler
- Allergien
- several meds and foods according to pt -too numerous to list
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
42 yo female patient with no PMH, here to receive the Pfizer COVID vaccine 1st dose. Approx. 10min after receiving the vaccine she felt "dizzy". Patient admitted that she just had Coffee this morning, also that she was scared and anxious before getting the vaccine. Denied any other symptom. Patient was evaluated by on-site EMS and MD. On physical exam noted to be AAO x 3; Initial VS: HR 80, RR 18, SpO2 98%, BP 150/95. Heart with RRR, lungs clear bilaterally. Patient was offered juice. After 15min observation patient felt better, repeated set of VS within normal limits. Patient was discharged with complete resolution of symptoms; was able to ambulate without any problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Pallor
Skin discolouration
Symptomtext
Patient received pfizer dose and went to charting area with mother. Patient began to feel dizzy and mother noticed a skin color change, said he looked "yellow". Patient did appear pale and diaphoretic. Mother held on to son to prevent a fall. Then child was brought to medical bay. Patient laid on cot, legs elevated, vital stable. Blood pressure 110/60, heart rate 103, pulse ox 98%. Patient sat up and left with mother once comfortable. Stable conditions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Dizziness
Hyperhidrosis
Immediate post-injection reaction
Symptomtext
Pt felt faint and got dizzy, light-headed, sweaty, and confused immediately after administration of vaccine. Pt has a history of vaccine phobia and admitted he was nervous prior to receiving the vaccine. He also informed me after he started to have side effects that his vaccine phobia had led to him not getting a vaccine since he was 14 years old.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Dizziness
Symptomtext
49yo M patient with no PMH, here to receive the Pfizer COVID vaccine booster. Approx. 10min after receiving the vaccine he felt "Dizzy". Patient admitted that he had just a small breakfast early this morning and that this has happened before when he is fasting. Claims that everything went well with the previous 2 vaccine doses. Denies any other symptom. Patient was evaluated by on-site EMS and MD. On physical exam noted to be AAO x 3; Initial VS: HR 76, RR 20, SpO2 98%, BP 120/86, capillary blood glucose: 82. Heart with RRR, lungs clear bilaterally. Patient was offered apple juice, he drank 12oz. After 15min observation patient felt better. He was discharged home with complete resolution of symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Decreased appetite
Dizziness
Feeding disorder
Insomnia
Malaise
Nausea
Symptomtext
The morning after I received my Covid-19 Booster injection, I became extremely nauseous. I waited it out because I was told that nausea can be one of the side effects. I increasingly became much much worse. I couldn't eat anything, felt like I wanted to vomit constantly (but never did vomit), and had really unbearable stomach cramping. I could not really sleep too well at all. Then on Sunday morning, I ate a piece of toast because I was feeling dizzier than what I had expected and knew I should eat something at least. My stomach became increasingly worse throughout the day, and in the late evening, I contacted my PCP's on-call service and requested help for the severe nausea and the doctor prescribed ZOFRAN for me. I took the dose immediately after picking it up from my pharmacy, but got little relief and I only slept a total of 2 fragmented hours of sleep. I took the second dose today, (3 days from my booster injection). however my stomach is still cramping pretty bad and I have no appetite and find it hard to even drink water because it seems to exacerbate my symptoms. I fear dehydration, so I am forcing myself to drink water. It's imperative i drink alot of water due to my Interstitial Cystitis Disease. I'm not feeling well at all.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- None. I was however, prescribed over the phone with my physician's office on-call, ZOFRAN RX
- Aktuelle Erkrankungen
- Interstitial Cystitis, Shoulder/Neck Pain from overly tight muscles
- Vorgeschichte
- interstitial Cystitis, Anxiety Disorder
- Andere Medikamente
- Lipitor, Tranxene, Protonix, Vitamin E, Vitamin D3, Iron, Magnesium, Zinc, Calcium
- Allergien
- Erythromycin, Keflex, Levaquin, Cipro, Elavil, Neurontin, Penicillin, Sulfa, Bactrim-DS, Estrace, Ceftin, Cefzil
- Vorherige Impfungen
- 61 yrs. old. After receiving both Covid-19 1st & 2nd dose injections, I felt extreme dizziness, and my chest felt very heavy
- Staat
- TN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 17.08.2023
- Impfdatum
- 24.01.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 295,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breakthrough COVID-19
Symptomtext
Covid-19 Breakthrough Infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- DM, COPD, CAD.
- Andere Medikamente
- No admission medication listed.
- Allergien
- Codeine, Homatropine, Hydrocodone, Prednisone, Cephalexin, Ibuprofen, Levofloxacin, Methocarbamol, Morphine, Telithromycin, Enoxaparin, ASA, Lactose, Adhesives
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 06.07.2023
- Impfdatum
- 07.01.2022
- Beginn
- 09.11.2022
- Tage bis Beginn
- 306,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Pfizer 3/19/21 lot# Er2613; Pfizer 4/9/21 lot# Ew0162; Pfizer 1/7/22 lot# FL3209
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 19.05.2023
- Impfdatum
- 17.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
no adverse reaction. Vaccine given beyond expiration date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- amoxicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 10.05.2023
- Impfdatum
- 16.01.2022
- Beginn
- 27.04.2023
- Tage bis Beginn
- 466,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Delusion
Depressed mood
Loss of personal independence in daily activities
SARS-CoV-2 test positive
Suicidal ideation
Symptomtext
Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: "Reason for Admission: depressed mood, paranoid delusions, suicidal thoughts, reduced self care, Covid-19 active infection Brief Summary of Hospital Stay: Medications started with Lexapro and Zyprexa and titrated to response. Tolerated medications. Encouraged participation in group therapy addressing reality testing and coping skills. Patient was mostly guarded during stay. Received a court order for treatment. Recovery from covid-19 was unremarkable."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 14,0
- Labordaten
- COVID detected PCR 4/21/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Severe recurrent major depression with psychotic features History of migraine headaches (Chronic) Arthrosis of left acromioclavicular joint Stress GAD (generalized anxiety disorder) (Chronic
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 05.05.2023
- Impfdatum
- 02.01.2023
- Beginn
- 14.04.2023
- Tage bis Beginn
- 102,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypersensitivity
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ALLERGIC REACTION, INIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypersensitivity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 03.05.2023
- Impfdatum
- 26.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Adverse event
Symptomtext
Adverse effect of other vaccines and biological substances, initial encounter on 2022-01-27.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Gender identity disorder, unspecified; Raynaud''s syndrome without gangrene; Excessive bleeding in the premenopausal period; Other specified abnormal findings of blood chemistry; Prophylactic measure, unspecified; Body mass index [BMI] 50.0-59.9, adult; Raynaud''s syndrome without gangrene; Folic acid deficiency; Dysmenorrhea, unspecified
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 02.05.2023
- Impfdatum
- 27.01.2021
- Beginn
- 23.02.2021
- Tage bis Beginn
- 27,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypersensitivity
Symptom recurrence
Symptomtext
ALLERGIC REACTION, INIT 3/9/2023 & 2/12/2023 -- RECURRENCE OF SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypersensitivity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 02.05.2023
- Impfdatum
- 10.01.2022
- Beginn
- 14.05.2022
- Tage bis Beginn
- 124,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Angioedema
Symptomtext
ANGIOEDEMA, INIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Angioedema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 18.01.2022
- Beginn
- 26.02.2023
- Tage bis Beginn
- 404,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
patient hospitalized
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 21.02.2023
- Impfdatum
- 07.01.2022
- Beginn
- 22.12.2022
- Tage bis Beginn
- 349,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Pfizer 4/1/21 Lot# Ew0153; Pfizer 5/21/21 Lot# Ew0183; Pfizer 1/7/22 Lot# FL3209
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 09.02.2023
- Impfdatum
- 24.01.2022
- Beginn
- 08.02.2023
- Tage bis Beginn
- 380,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 02.02.2023
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Child, age 10, was given Covid-19 Pfizer\ BioNTech vaccine dose for 12+ - no adverse effect were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- -
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 21.09.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 102,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 21Sep2022 as dose 5 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation; BNT162b2 (BNT162B2), on 17Sep2021 as dose 1, single (Lot number: EW0184), as dose 2, single (Lot number: FL3209 ) (Lot number also reported as FL3209 / HT326; vaccine administration date for dose 2 also reported as 06Apr2022, pending confirm), on 02Mar2022 as dose 3 (booster), single (Lot number: ENG6208) and on 13Apr2022 as dose 4 (booster), single (Lot number: ER8729) for covid-19 immunisation. The patient's relevant medical history included: "Crohn's Disease" (unspecified if ongoing); "Stroke" (unspecified if ongoing); "Malaria" (unspecified if ongoing); "Colon removed" (unspecified if ongoing). Concomitant medication(s) included: ATORVASTATIN, start date: 10Sep2022, stop date: 16Jan2023. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jan2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures paxlovid from 17Jan2023 to 21Jan2023 were taken as a result of drug ineffective, covid-19. The information on the batch/lot number for BNT162b2, BNT162b2 omi ba.4-5 has been requested and will be submitted if and when received.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300040084 Same patient/product, different dose different event.;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Colon operation; Crohn's disease; Malaria; Stroke
- Andere Medikamente
- ATORVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Tinnitus
Symptomtext
Ringing in ears
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- Hearing test 11/16/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hashimoto's
- Andere Medikamente
- Synthroid
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 13.01.2021
- Beginn
- 10.01.2023
- Tage bis Beginn
- 727,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Nasopharyngitis
SARS-CoV-2 test positive
Symptomtext
Tested positive for COVID-19 on 1/10/23 presenting with mild cold symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID-19 Rapid Antigen Test 1/10/23
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Dementia, Hypertension, Hypothyroidism, Type 2 Diabetes Mellitus, Aortic valve sclerosis, GERD, Cardiac murmur, COPD, hyperlipidemia, Vitamin D deficiency, renal calculi, osteopenia
- Andere Medikamente
- Divalproex sodium, Colace, Fluoxetine, Levothyroxine, Omeprazole, Quetiapine fumarate, Trazodone, Valsartan, Apap, Bisacodyl, compro supp, Hyosyne
- Allergien
- Vioxx, Sulfur, Lipitor, Cephalosporins, HCTZ, Rofecoxib, Trimethoprim
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 02.01.2023
- Impfdatum
- 06.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Aortic valve replacement
Blood test abnormal
Cardiac operation
Cardiac valve disease
Echocardiogram abnormal
Endocarditis
Infection
Mitral valve replacement
Symptomtext
Myocarditis followed by deteriorated heart valves resulting in open heart surgery for aorta and mitral valve replacement. Surgery in June 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aortic valve replacement
- Hospital-Tage
- 60,0
- Labordaten
- Echocardiagram showing valve deterioration, blood work showing infection, heart inflammation.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Percocet and other narcotic based drugs
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 02.01.2023
- Impfdatum
- 15.06.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was vaccinated beyond use date of 5/6/2022. No symptoms reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None Reported
- Vorgeschichte
- None Reported
- Andere Medikamente
- None Reported
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 02.01.2023
- Impfdatum
- 06.06.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was vaccinated beyond use date of 5/6/2022. No symptoms reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None Reported
- Vorgeschichte
- None Reported
- Andere Medikamente
- None Reported
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 02.01.2023
- Impfdatum
- 16.05.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was vaccinated beyond use date of 5/6/2022. No symptoms reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None Reported
- Andere Medikamente
- None reported
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 14.11.2022
- Impfdatum
- 13.04.2021
- Beginn
- 17.05.2021
- Tage bis Beginn
- 34,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dry eye
Eye discharge
Eye swelling
Eyelid margin crusting
Lacrimation increased
Ocular hyperaemia
Photophobia
Swelling of eyelid
Temperature intolerance
Symptomtext
Approximately 2 weeks after my second vaccine, I started experiencing significant eye problems including: chronic redness, swollen eyes, swollen eye lids, sensitivity to light, dry eyes, chronic and constant tearing that does not stop, sensitivity to changes in temperatures, sensitivity to things I don't even understand. I can just be in a room and my eyes will start tearing uncontrollably. At times, they get mucus like film. Every single day since the second vaccine I wake up with my eyes crusted shut. There is no relief from any eye drops the opthomologists have given me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dry eye
- Hospital-Tage
- -
- Labordaten
- I have seen two ophthalmologists from the Eye Institute, as well as an an opthomologist from a local Clinic. None of them were aware of the connection between the Pfizer vaccine and eye issues. Honestly, they really didn't seem to care. They have treated me symptomatically for dry eyes with Xidra, Systane, Retain, Renew. I take Zyrtec and Nasacort in case these symptoms are related to allergies. However, absolutely nothing has helped. The problem and symptoms have never stopped, there is no relief. I had no eye issues prior to receiving the vaccines. I did one booster on January 3, 2022 and my eyes became significantly worse. I have been to multiple visits to the Eye Institute and they have given me multiple tests. There is no conclusion as to what is causing the ongoing problems. I have another visit scheduled for 11/21/2022 with another opthomologist who specializes in uveitis.
- Aktuelle Erkrankungen
- None. I have never had any eye problems.
- Vorgeschichte
- I have hypothyroidism.
- Andere Medikamente
- Levothyroid, Armour Thyroid
- Allergien
- Shellfish, pollen, dust, mold, erythromycin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 24.10.2022
- Impfdatum
- 25.01.2022
- Beginn
- 18.10.2022
- Tage bis Beginn
- 266,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case after three admissions Pfizer 7/1/21 Lot# Ew0181; Pfizer 7/22/21 Lot#FA7485; Pfizer 1/25/22 Lot# FL3209
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- F
- Eingang
- 15.10.2022
- Impfdatum
- 04.02.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 199,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A female patient received BNT162b2 (BNT162B2), on 08Jan2021 as dose 1, single (Lot number: EL3246), on 27Jan2021 as dose 2, single (Lot number: EL3246), on 23Aug2021 as dose 3 (booster), single (Lot number: FC3180) and on 04Feb2022 as dose 4 (booster), single (Lot number: FL3209) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant) with onset 22Aug2022, outcome "unknown", COVID-19 (medically significant) with onset 22Aug2022, outcome "recovered" and all described as "COVID-19 ". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (22Aug2022) Positive, notes: she had covid on 22Aug2022, tested positive. The clinical course was reported as follows: on 22Aug2022 of this year, she tested positive for COVID-19. For 19 days, she tested positive, and she is calling to find out how long she will be protected and when can she get the booster dose. So, I have all of the dates of the doses that she received. Her first dose, and they are all Pfizer COVID-19 Vaccines. First dose was 08Jan2021 with LOT# EL3246. Her second primary dose was 27Jan2021 with LOT# EL3246. Her first booster dose was 23Aug2021 and the LOT# is FC3180 and her second booster, the last booster was 04Feb2022 this year and that would be LOT# was FL3209 and like I mentioned, on 22Aug2022 she tested positive after this. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220822; Test Name: Covid-19 test; Test Result: Positive ; Comments: she had covid on 22Aug2022, tested positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 12.10.2022
- Impfdatum
- 21.01.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 264,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Symptomtext
Patient developed COVID-19 post vaccination for same.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
pt was given expired covid vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes hypertension hypothyroidism
- Andere Medikamente
- n/a
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 12.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Pt was given expired covid vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- type 2 Diabetes, Hypertension, CKD
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
pt was given an expired vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hot flush
Hyperhidrosis
Symptomtext
hot flashes; excessive sweating; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient received BNT162b2 (BNT162B2), on 26Feb2022 as dose 3 (booster), single (Lot number: FL3209) at the age of 61 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (dose 2, Batch/Lot No: EW0170), administration date: 20Apr2021, when the patient was 60-year-old, for COVID-19 Immunization; BNT162b2 (dose 1, Batch/Lot No: ER8732), administration date: 30Mar2021, when the patient was 60-year-old, for COVID-19 Immunization. The following information was reported: HYPERHIDROSIS (non-serious) with onset 26Feb2022, outcome "recovered" (2022), described as "excessive sweating"; HOT FLUSH (non-serious) with onset 26Feb2022, outcome "recovered" (2022), described as "hot flashes". Therapeutic measures were not taken as a result of hot flush, hyperhidrosis. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hot flush
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 30.09.2022
- Impfdatum
- 31.03.2022
- Beginn
- 27.09.2022
- Tage bis Beginn
- 180,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Blood test normal
Dysstasia
Fall
Symptomtext
I could hardly stand up I lost my balance and fell, I took blood pressure and it was 80/40. Once I took my blood pressure I called my doctor to let him know I had fallen. I had an emergency appointment for the following day where he ordered blood work. He took me off of all of my blood pressure related medications. I am now back to walking a mile and doing my normal daily activities.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Balance disorder
- Hospital-Tage
- -
- Labordaten
- Blood work - nothing out of the ordinary.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Amlodipine; ULTRAM; oxybutynin; hydrochlorothiazide; benazepril; PROLIA
- Allergien
- Iodine
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 28.09.2022
- Impfdatum
- 29.03.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 41,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy breast abnormal
Breast conserving surgery
Intraductal proliferative breast lesion
Mammogram abnormal
Pathology test
Precancerous cells present
Radiotherapy
Symptomtext
In June of 2022 had an abnormal mammogram. Needle biopsy in July showing precancerous cells. Doctor performed lumpectomy on August 4th. Pathology on the lump showed Ductal carcinoma in situ and the doctor began radiation and I completed my last round of radiation on Monday September 26th. On October the 3rd I begin anastrozole 1mg per day for the next 5 years.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy breast abnormal
- Hospital-Tage
- -
- Labordaten
- Mammogram - showed irregularities. Needle Biopsy- showed precancerous cells. Lumpectomy - showed Ductal carcinoma in situ.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High blood pressure; high cholesterol
- Andere Medikamente
- Lisinopril; aspirin; simvastatin; PREMARIN vaginal cream; ca; coQ10; fish oil; multivitamin; famotidine
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 03.01.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 256,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough case dose 1 Pfizer 2/5/21 EL9269 dose 2 Pfizer 2/26/21 EN6198
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ test on 9/16/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 19.09.2022
- Impfdatum
- 02.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test abnormal
Magnetic resonance imaging spinal abnormal
Neuropathy peripheral
Sensory loss
Spinal X-ray abnormal
Spinal osteoarthritis
Symptomtext
Woke up and could not feel my feet completely. Called doc off at Medical and had a telehealth appointment with. I explained that I had had the COVID booster 5 days before and not sure if it was reported. She placed me on gabapentin for neuropathy due to possible sciatic issues and it helped slightly- changed providers. Was sent for X-rays, MRI, blood work.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test abnormal
- Hospital-Tage
- -
- Labordaten
- X-rays MRI blood work - found to have degenerative spine but wanted to report just in case since it came so fast with no sign of gradual issue and only 5 days after shot.
- Aktuelle Erkrankungen
- Seasonal allergic asthma
- Vorgeschichte
- Seasonal allergic asthma
- Andere Medikamente
- Zyrtec, Flonase, Escitalpram 10mg
- Allergien
- Percocet, Methocarbamol, Meloxicam
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.09.2022
- Impfdatum
- 10.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
SARS-CoV-2 test
Vertigo
Symptomtext
Vertigo/Booster was about 20 days later; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 10Jan2022 as dose 3 (booster), single (Lot number: Fl3209), in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: SPIRONOLACTONE. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot number: ER8731, Anatomical location: Arm Left), administration date: 14Apr2021, for Covid-19 immunisation, reaction(s): "vertigo"; BNT162b2 (DOSE 2, SINGLE, Lot number: EW0173, Anatomical location: Arm Left), administration date: 07May2021, for Covid-19 immunisation, reaction(s): "Vertigo". The following information was reported: VERTIGO (non-serious) with onset 2022, outcome "recovered", described as "Vertigo/Booster was about 20 days later". The event "vertigo/booster was about 20 days later" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of vertigo. Additional information: The patient experienced vertigo with all the three doses and afraid to get second booster. The patient did not have any other vaccines in four weeks. The patient had no covid-19 prior to vaccination. The patient was tested negative for Covid-19 post vaccination. The patient had no known allergies and other medical history. Other medications in two weeks included Multi vitamins.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201157238 Same patient/Vaccine/event, different dose;US-PFIZER INC-202201157337 Same patient/Vaccine/event, different dose;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- SARS-CoV-2 test
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220902; Test Name: Covid-19 test; Test Result: Negative ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No, known allergies: No
- Andere Medikamente
- SPIRONOLACTONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 17.09.2022
- Impfdatum
- 11.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Nurse) from product quality group. The reporter is the patient. A 33-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 29Jan2021 at 10:00 as dose 1, single (Lot number: EN9581), in right arm, on 19Feb2021 at 10:00 as dose 2, single (Lot number: EL9266), in left arm and on 11Feb2022 at 10:00 as dose 3 (booster), single (Lot number: FL3209) at the age of 33 years, in left arm for covid-19 immunization. The patient's relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing); "Diabetes type 1" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Ibuprofen, reaction(s): "Known allergies: Ibuprofen". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of vaccination failure, covid-19. Paxlovid treatment was from 06Sep202 to 07Sep2022.; Sender's Comments: As there is limited information in the case provided, the causal association between the reported events with the suspect drug BNT162B2 cannot be excluded. The case will be reassessed once new information is available.,Linked Report(s) : US-PFIZER INC-202201151177 Same reporter/patient, same drug/different dose, different event.;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 test; Test Result: Positive ; Comments: Treatment of COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy; Type 1 diabetes mellitus
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 31.08.2022
- Impfdatum
- 15.01.2022
- Beginn
- 18.08.2022
- Tage bis Beginn
- 215,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Pt tested positive for COVID on 08/18/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 23.08.2022
- Impfdatum
- 01.04.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 275,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
COVID-19
Electrocardiogram
Interchange of vaccine products
Panic attack
Thyroid function test
Symptomtext
After getting covid in January 2022, I started to have panic attacks lasting several days. It happened first in January, when I had covid. Then again in June and July 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- EKG, thyroid level tested, blood tests for heart health
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- General anxiety, depression, narcolepsy, migraines with aura
- Andere Medikamente
- Zoloft 100mg daily, provigil 100mg three times a day, Wellbutrin 75mg twice a day, skyla IUD
- Allergien
- Penicillin, amoxicillin, sulfa
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 18.08.2022
- Impfdatum
- 29.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter (Consumer or other non-HCP). A 33-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 29Dec2021 as dose 3 (booster), single (Lot number: FL3209) at the age of 33 years for COVID-19 immunisation; COVID-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "recovering" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive; (31Jul2022) Negative; (05Aug2022) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 included PF-07321332, ritonavir (PAXLOVID) with treatment start date: 26Jul2022, treatment stop date: 31Jul2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID test; Test Result: Positive ; Test Date: 20220731; Test Name: COVID test; Test Result: Negative ; Test Date: 20220805; Test Name: COVID test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- -
- Geschlecht
- M
- Eingang
- 13.08.2022
- Impfdatum
- 11.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 79-year-old male patient received BNT162b2 (BNT162B2), on 05Feb2021 at 10:00 as dose 1, single (Lot number: en5318), in right arm, on 26Feb2021 at 12:00 as dose 2, single (Lot number: en6203), in right arm, on 06Oct2021 at 12:00 as dose 3 (booster), single (Lot number: ff8841), in right arm and on 11Apr2022 at 12:00 as dose 4 (booster), single (Lot number: fl3209), in right arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Paxlovid (Lot number: 00069108530) was started on 29Jun2022 and stopped on 01Jul2022 for the treatment of COVID-19. Other medications in 2 weeks was reported to be unknown. There were no known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Test; Test Result: Positive ; Comments: Treatment of COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 07.08.2022
- Impfdatum
- 16.02.2022
- Beginn
- 07.08.2022
- Tage bis Beginn
- 172,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asymptomatic COVID-19
COVID-19
SARS-CoV-2 test positive
Symptomtext
Resident asymptomatic at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- Resident Rapid tested positive for covid today 8/7/22 results POSITIVE.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypothyroidism; Hyperlipidemia
- Andere Medikamente
- -
- Allergien
- Aricept; Bactrim; Lasix; Codeine; Naproxen
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 05.08.2022
- Impfdatum
- 06.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19 treatment; COVID 19 treatment; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 41-year-old male patient received BNT162b2 (BNT162B2), on 06Jan2022 as dose 4 (booster), single (Lot number: FL3209) at the age of 41 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Negative, notes: tested negative on Ag test on day 5 post-dose; Negative, notes: I tested negative on Ag again on day 9 post-dose; Positive, notes: I tested positive by home Ag on day 11; Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The had no known allergies. The patient was treated with Paxlovid from 23Jul2022 to 27Jul2022 for COVID-19. The patient completed his course of Paxlovid and tested negative on Ag test on day 5 post-dose, with complete resolution of symptoms. He tested negative on Ag again on day 9 post-dose. On day 10 post-dose he developed sneezing and nasal congestion. He tested positive by home Ag on day 11.; Sender's Comments: Based on the known safety profile and Limited information in the case report a casual association between LOE events and suspect drug BNT162B2 cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Ag test; Test Result: Negative ; Comments: tested negative on Ag test on day 5 post-dose; Test Name: Ag test; Test Result: Negative ; Comments: I tested negative on Ag again on day 9 post-dose.; Test Name: Ag test; Test Result: Positive ; Comments: I tested positive by home Ag on day 11.; Test Name: Ag test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 04.08.2022
- Impfdatum
- 04.08.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
14 y/o M patient brought to clinic by mother for Covid 19 booster. Mother presented pt's CDC vaccine card with 2 doses of Pfizer from Sept 2021 written on it. Pt received dose of purple cap 12&up pfizer today. Upon entering vaccine into Pt's module in EMR, it was noted pt already had a booster in April 2021. Mother was unaware of this April 2021 booster because father had brought the patient in without notifying mother. Mother was educated on s/s of myocarditis and advised to bring pt in for signs of illness/infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ADHD Medication
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 03.08.2022
- Impfdatum
- 09.03.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 146,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nasal congestion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nasal congestion
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 15.01.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 193,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Tested positive for Covid; Tested positive for Covid; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 16-year-old male patient received BNT162b2 (BNT162B2), on 21May2021 as dose 1, single (Lot number: EW0177) intramuscular, on 18Jun2021 as dose 2, single (Lot number: EW0177) and on 15Jan2022 as dose 3 (booster), single (Lot number: FL3209) at the age of 16 years intramuscular for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 27Jul2022, outcome "recovering" and all described as "Tested positive for Covid". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (27Jul2022) Positive, notes: covid test type post vaccination: Nasal Swab. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Clinical course: The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19. No follow-up attempts are possible. No further information is expected
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220727; Test Name: SARS-CoV-2 test; Test Result: Positive ; Comments: covid test type post vaccination: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 30.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 74-year-old male patient received BNT162b2 (BNT162B2), on 30Mar2022 as dose 4 (booster), single (Lot number: FL3209) at the age of 74 years, in left arm for Covid-19 immunisation; CoviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for Covid-19 immunisation. The patient's relevant medical history included: "High Blood Pressure" (unspecified if ongoing); "Prostate Cancer" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID". Therapeutic measures were taken as a result of drug ineffective, Covid-19. Clinical course: Patient received treatment of Covid-19 (Brand: Pfizer) from 12Jul2022 to 16Jul2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high; Penicillin allergy; Prostate cancer
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 21.03.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 130,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
positive covid test in fully vaccinated and boosteredx2 pt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 29.07.2022
- Impfdatum
- 13.01.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 168,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 22-year-old male patient received BNT162b2 (BNT162B2), on 15Apr2021 as dose 1, single (Lot number: ER8729), on 06May2021 as dose 2, single (Lot number: EW0172) and on 13Jan2022 as dose 3 (booster), single (Lot number: FL3209) at the age of 21 years for covid-19 immunisation. The patient's relevant medical history included: "hashimotos hypothryroid" (unspecified if ongoing), notes: hashimotos hypothryroid; "Obesity" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID. The patient received other medications in 2 weeks after vaccination. Past drug history included: Zithromax, reaction(s): "Known allergies: zithromax", notes: Known allergies: zithromax. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 30Jun2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (30Jun2022) Positive, notes: First day of Positive test; (Jul2022) Positive, notes: but still rapid positive; (20Jul2022) Positive, notes: Day-21 still showing positive rapid testing. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: First day of positive test, second day of bad symptoms. Took 5 days treatment. Around day 9-10 of COVID infection, symptoms returned serious head congestion, sinus pain. Day 21 and still showed positive rapid testing. Symptoms were much better, but still rapid positive. The patient received Paxlovid as treatment from 30Jun2022 to 04Jul2022 for COVID 19. Doxy antibiotic for sinus infection. Patient assumed this was rebound. Device Date reported on 21Jul2022. No follow-up attempts possible. No further information expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220630; Test Name: rapid testing; Test Result: Positive ; Comments: First day of Positive test; Test Date: 202207; Test Name: rapid testing; Test Result: Positive ; Comments: but still rapid positive; Test Date: 20220720; Test Name: rapid testing; Test Result: Positive ; Comments: Day-21 still showing positive rapid testing
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hashimoto's thyroiditis (hashimotos hypothryroid); Obesity
- Andere Medikamente
- SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 28.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Upon entering information into system It was noted that the patient received her second booster earlier then schedule released by CDC. Vaccine series is as follows: Pfizer 3/31/21, Pfizer 4/21/21, Pfizer 4/27/22 and Pfizer 7/27/22. I attempted to contact patient at phone number listed on consent form to advise her of the information and obtain additional information, but have been unable to speak with her as of yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- unk
- Vorgeschichte
- unk
- Andere Medikamente
- unk
- Allergien
- unk
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 27.07.2022
- Impfdatum
- 29.01.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 178,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID BREAKTHROUGH CASE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID+ 7/26/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 03.02.2021
- Beginn
- 23.07.2022
- Tage bis Beginn
- 535,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
COVID infection resulting in hospitalization
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 3,0
- Labordaten
- COVID PCR 7/23/22
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Recent COVID-19 infection without acute respiratory symptoms History of bladder cancer with partial resection Type 2 diabetes mellitus Normocytic anemia Iron deficiency anemia GERD
- Andere Medikamente
- simvastatin
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 24.07.2022
- Impfdatum
- 30.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49-year-old male patient received BNT162b2 (BNT162B2), on 30Jan2022 as dose 3 (booster), single (Lot number: FL3209) at the age of 48 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: DILTIAZEM; CRESTOR; ZETIA; OLMESARTAN; PRILOSEC [OMEPRAZOLE]; FINASTERIDE; XYZAL. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: started testing positive again; Positive, notes: Symptoms fully returned 5 days after completing Paxlovid treatment, started testing positive again. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Course: The patient received anti viral treatment (Paxlovid) from 08Jul2022 to 12Jul2022 for COVID 19 Treatment. The symptoms fully returned 5 days after completing Paxlovid treatment, started testing positive again. No follow-up attempts are required. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19; Test Result: Positive ; Comments: started testing positive again.; Test Name: Covid-19; Test Result: Positive ; Comments: Symptoms fully returned 5 days after completing Paxlovid treatment, started testing positive again.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- DILTIAZEM; CRESTOR; ZETIA; OLMESARTAN; PRILOSEC [OMEPRAZOLE]; FINASTERIDE; XYZAL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 03.01.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 199,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient fully vaccinated, but tested positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 13.02.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 110,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Nasal congestion
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case. Allergies started flaring up with nasal congestion. Took Home test and it was Positive. Quarantined and took a lot of vitamins. Five days later he felt better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- Severe Allergies
- Andere Medikamente
- Multivitamin
- Allergien
- Dust
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 24.01.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 169,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 28.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Menstruation delayed
Symptomtext
has not had a period since her shots; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the parent. A 15-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Jan2022 at 11:00 as dose 2, single (Lot number: FL3209) at the age of 15 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot number: FJ8762, Administration time: 11:00 AM, Vaccine location: Left arm), administration date: 05Jan2022, when the patient was 15-year-old, for Covid-19 Immunization, reaction(s): "has not had a period since her shots". The following information was reported: MENSTRUATION DELAYED (non-serious), outcome "not recovered", described as "has not had a period since her shots". Therapeutic measures were not taken as a result of menstruation delayed. Additional Information: Facility type vaccine was reported as Doctor's office/urgent care. Additional information: Patient was not received any other vaccine four weeks prior vaccination and patient did not receive any medication two weeks prior vaccination. Patient not diagnosed with covid-19 prior to vaccination and since vaccination patient not tested for covid-19. The patient had no known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstruation delayed
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: No adverse event (Other medical history: No)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 31.01.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 157,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 21.01.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 94,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abortion spontaneous
Exposure during pregnancy
Symptomtext
Miscarriage on April 25, 2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abortion spontaneous
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 16.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 75-year-old male patient received BNT162b2 (BNT162B2), on 18Jan2021 at 10:00 as dose 1, single (Lot number: FL2249), in left arm, on 08Feb2021 at 13:00 as dose 2, single (Lot number: FL9262), in left arm, on 18Aug2021 at 09:00 as dose 3 (booster), single (Lot number: FD8448), in left arm and on 16Feb2022 at 10:00 as dose 4 (booster), single (Lot number: Fl3209) at the age of 75 years, in left arm for covid-19 immunization. The patient's relevant medical history included: "CVID" (unspecified if ongoing), notes: Have CVID take subcutaneous, Xembify weekly. The patient had no known allergies. Concomitant medication(s) in 2 weeks included: XEMBIFY, start date: 31May2021. The following information was reported: VACCINATION FAILURE (medically significant), outcome "unknown", COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown results; virus free, notes: Tested almost virus free; Positive, notes: Test showed strong virus presence, stronger than any prior test. Therapeutic measures were taken as a result of covid-19. It was reported that, the patient felt better after third day, completed the course. Tested almost virus free. A couple of days symptoms flared back up and got worse than before treatment. Test showed strong virus presence, stronger than any prior test. Started running a fever again. Still felt pretty lousy. Anti-viral details: Product: COVID 19 Treatment, Brand: Paxlovid, Treatment start date was on 10Jun2022 and treatment stop date was on 14Jun2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID 19; Result Unstructured Data: Test Result:Unknown results; Test Name: COVID 19; Result Unstructured Data: Test Result:virus free; Comments: Tested almost virus free; Test Name: COVID 19; Test Result: Positive ; Comments: Test showed strong virus presence, stronger than any prior test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Common variable immunodeficiency (Have CVID take subcutaneous Xembify weekly)
- Andere Medikamente
- XEMBIFY
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 25.06.2022
- Impfdatum
- 28.01.2022
- Beginn
- 30.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase normal
Bacterial test
Blood immunoglobulin M increased
Chromaturia
Glomerulonephritis
Haematuria
Inflammation
Laboratory test normal
Proteinuria
Red blood cells urine
Urinary occult blood
Urine abnormality
Urine leukocyte esterase positive
White blood cells urine positive
Symptomtext
It's glomerulonephritis. Inflammation of the kidneys, such as proteinuria, hematuria, and bacteria. It started a few days after the booster shot. It is still under way. It has also become a lifelong condition to be treated. My daughter is only 13 years old. She needs to get vaccinated and take medicine for life.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alanine aminotransferase normal
- Hospital-Tage
- -
- Labordaten
- ALT : 5L IMMUNOGLOBULIN M : 219H URINE COLOR : RED APPEARANCE : TURBID OCCULT BLOOD : 3+ PROTEIN : 2+ LEUKOCYTE ESTERASE : 1+ WBC : 6-10 RBC : > OR=60 BACTERIA : FEW
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None She is very healthy.
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 11.06.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
Patient: 9/22/21- First dose of Pfizer vaccine administered 0.3 ml 5/17/22- 2nd dose Pfizer vaccine administered 0.3 ml 6/11/22- 3rd dose of Pfizer vaccine administered 0.3 ml Spoke with patient on 6/21/22 upon discovery of 3rd dose. . She reports that due to the long interval of time that passed since her first vaccine on 9/22/21, she was under the assumption that she needed to restart her vaccine series therefore she filled out a first dose consent at her 5/17/22 appointment, and a second dose consent at her 6/11/22 appointment. Patient was made aware that she did not need to receive the 3rd dose and that the 9/22/21 and 5/17/22 completed her initial vaccine series. Director of Community Health Services notified of incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 16.06.2022
- Impfdatum
- 09.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non-HCP) from product quality group. The reporter is the patient. An 82-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Apr2022 at 09:00 as dose 4 (booster), single (Lot number: FL3209) at the age of 81 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 3 (booster), single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Course: Tested positive (after negative antigen test) 7 days after stopped treatment with Paxlovid. Symptoms included runny nose, fatigue, and cough. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- -
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 26.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Physician). An elderly male patient received BNT162b2 (BNT162B2), on 26Feb2022 as dose 4 (booster), single (Lot number: FL3209), in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing); "Hypercholersterolemia" (unspecified if ongoing); "Penicillin allergy" (unspecified if ongoing). Concomitant medication(s) included: IRBESARTAN oral, start date: 01Jan2022, stop date: 24May2022; ROSUVASTATIN oral, start date: 01Jan2022, stop date: 06May2022. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: COVID relapse, notes: low cycle threshold on PCR testing. Therapeutic measures were taken as a result of covid-19. Clinical Course: Anti-viral details, covid-19 Treatment was Paxlovid started on 07May2022 to 11May2022. Covid relapse 5 d after d/c Paxlovid with low cycle threshold on PCR testing.; Sender's Comments: Based on reported information, causal association of event drug ineffective, covid-19 with BNT162b2 cannot be excluded. However, response to vaccine can vary in individuals.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: PCR; Result Unstructured Data: Test Result:COVID relapse; Comments: low cycle threshold on PCR testing
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypercholesteremia; Hypertension; Penicillin allergy
- Andere Medikamente
- IRBESARTAN; ROSUVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
Patient's guardian entered the incorrect date of birth on patient's vaccination form making the patient appear to be 13 years old instead of his actual age of 9 years. The date of birth/age of patient was not verified by the pharmacy and the patient was given an adult dose of pfizer instead of a pediatric dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- N/A
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 26.05.2022
- Impfdatum
- 20.01.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 126,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated and boosted times 1. COVID breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
vaccine administered outside of beyond use date- not supported by vaccine manufacturer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
vaccine administered outside the beyond use date- not supported by vaccine manufacturer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered outside of beyond use date-not supported by vaccine manufacturer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine given beyond use date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 13.01.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 125,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asymptomatic COVID-19
SARS-CoV-2 test positive
Symptomtext
positive covid test in fully vaccinated and boostered, asymptomatic pt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
Patient received Pfizer like her second vaccine instead of Moderna. No side effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 06.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 35-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 06Jan2022 as dose 3 (booster), single (Lot number: FL3209) at the age of 34 years, in left arm for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 04May2021 as dose 1, single (Lot number: 003C21A), in left arm and on 01Jun2021 as dose 2, single (Lot number: 049C21A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Interchange of vaccine products" (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of covid-19. Clinical course: Other medication in 2 weeks was reported as no. No Known allergies.; Sender's Comments: Based on the information in the case report, a possible causal relationship between reported events and suspect drug BNT162B2 cannot be excluded
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Interchange of vaccine products
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Improper storage of vaccine, deemed non-viable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 08.01.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 52,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia areata
Symptomtext
Four large patches of hair have fallen out (Alopecia Areata) since date of third (booster) dose of Pfizer COVID-19 vaccine. Hair loss discovered on 3/17/2022 and has worsened since that date. Approximately 50% of my hair is now gone; have never had occurrence of AA in the past
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alopecia areata
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity, Panic Disorder, Depression
- Andere Medikamente
- Duloxetine 60 mg, Omeprazole, Clonazepam 0.5 mg (2x per day)
- Allergien
- Allergic reaction to Blisovi Fe (widespread rash) after taking for one week
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 14.04.2021
- Beginn
- 01.03.2022
- Tage bis Beginn
- 321,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest discomfort
SARS-CoV-2 test positive
Symptomtext
03/01/22 presents to ED for "Chest pressure". PMHx of "HTN, HLD, CKD stage 4, polycystic liver and kidney disease, atypical brain meningioma s/p resection/radiation and seizure disorder"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 03/01/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Improper storage of vaccine, deemed non-viable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 08.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blood test
Chorioretinitis
Choroiditis
Laboratory test
Macular oedema
Magnetic resonance imaging
Metamorphopsia
Visual impairment
Symptomtext
Patient used to have 20/20 vision. A little after one week of her vaccination, patient reported a grey blob blocking her central vision along with distortion that continued to get worst. We thought it was anxiety at first but took her to the eye doctor on February 5. They found posterior uveitis and macular edema and her vision had reduced to 300/20. They immediately sent us to retina specialists. Since then, we have seen multiple specialists to try to figure out what was going on. She has been diagnosed with ampiginous choroiditis. She is on prednison and Cellcept to try to stop the inflammation and restore vision. Her vision has improved but is around 125/20. We are still trying to restore vision.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- There are way too many to list. WE have been in and out of doctors for months. She has had full bloodwork analysis, MRI, and multiple eye exams.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None other than ADHD
- Andere Medikamente
- Ritalin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 15.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Symptomtext
Two weeks after I received the vaccination my hair stylist noticed I had hair loss. She had not noticed this hair loss six weeks prior at my previous appointment. I went to see a dermatologist who prescribed a topical solution that I have been using on the patches where my hair is thinning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alopecia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Nexletol; Vitamin D; Vitamin B; Aspirin; COQ10; Fish oil
- Allergien
- NKDA; NKFA
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
Patient received primary vaccine series at local Assistance Campus on 3/5/2021 and 4/2/2021. She then went to pharmacy for what should have been her booster dose on 1/18/2022. She returned to pharmacy and received a 4th dose on 2/8/2022. The pharmacy store did not check the state registry for documentation. The 4th dose had not been approved at the time of this administration. And even given the 2nd booster approval, it was administered too early.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 25.04.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient received adult dose instead of pediatric dose of Pfizer. 1 day before 12th birthday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NO
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- asthma
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 17.01.2022
- Beginn
- 13.02.2022
- Tage bis Beginn
- 27,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Computerised tomogram kidney abnormal
Nephrolithiasis
Symptomtext
I developed a kidney stone on the right kidney. I have never had a kidney stone before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- Bloodwork panel done; CT scan of kidney
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Metronitozodol Gel; Vitamin B13; Omnicertane
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 28.03.2022
- Beginn
- 10.04.2022
- Tage bis Beginn
- 13,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Menstruation delayed
Symptomtext
Menstrual-period is 5 days late
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstruation delayed
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 26.01.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 27,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Caesarean section
Delivery
Exposure during pregnancy
Multigravida
Symptomtext
Hospitalized on 2/22/22 for scheduled repeat cesarean section G2, P1-0-0-1 at 39 weeks gestation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Caesarean section
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 29.01.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 27,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Exposure during pregnancy
Forceps delivery
Postpartum disorder
Symptomtext
Patient hospitalized for forceps-assisted vaginal delivery. Following delivery, the patient had an uncomplicated postpartum course. No information given on baby. This was within 6 weeks of receiving covid vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure during pregnancy
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 31.01.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Small intestinal obstruction
Symptomtext
Patient hospitalized for SBO (small bowel obstruction) , Acute renal failure (ARF) within 6 weeks of receiving covid vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute kidney injury
- Hospital-Tage
- 17,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 12.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 19,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Intentional overdose
Suicidal ideation
Symptomtext
Intentional drug overdose; suicidal ideation. Behavioral health admission and treatment. Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intentional overdose
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product preparation issue
Symptomtext
PFIZER VACCINE WAS ADMINISTERED UNDILUTED. THE PATIENT WAS INFORMED BY THE PHARMACIST. THEN THE PHYSICIAN OFFICE WAS CALLED AND LEFT THE MESSAGE WITH THE OFFICE. NOTIFIED THE CLINICAL COORDINATOR AND THE DISTRICT OFFICE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- NOT APPLICABLE
- Aktuelle Erkrankungen
- WRIST FRACTURE
- Vorgeschichte
- GENERAL PAIN
- Andere Medikamente
- NO
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 20.01.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 20,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Intentional product misuse
Major depression
Suicide attempt
Symptomtext
Patient admitted because of intentional acetaminophen ingestion (today patient states she ingested ibuprofen) as a suicide attempt. Current severe episode of major depressive disorder without psychotic features without prior episode. Behvioral health admission and treatment. Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intentional product misuse
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 01.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Sudden hearing loss
Tinnitus
Symptomtext
Sudden hearing loss then ringing in right ear
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- Hearing tests - 1/27/22, 1/28/22, 1/31/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi vitamin Vitamin D
- Allergien
- Penicillin
- Vorherige Impfungen
- Temporary SSHL occurred 12 days after 2nd Pfizer Covid shot in June 2021. Connection between shot and temporary hearing loss wa
- Staat
- -
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 05.01.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 42,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Patient had an ED visit and/or hospitalization within 6 weeks of receiving COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 27.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine may have been store under condition that depart from the manufacture's recommended specification, so the manufacturer deem vaccine not viable and recommends repeated dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 27.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine may have been store under condition that departed from the manufacturer recommended specification, so the manufacturer deem vaccine not viable and recommended a repeat dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 27.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine may have been store under condition that departed from the manufacturer's recommended specification, so the manufacturer deem vaccine not viable and recommended a repeat dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 27.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Poor quality product administered
Product storage error
Symptomtext
Vaccine may have been store under condition that depart from the manufacture's recommended specification, so the manufacture deem vaccine not viable and recommends a repeat dose of vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- not indicated
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 26.03.2022
- Impfdatum
- 26.03.2022
- Beginn
- 26.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Poor quality product administered
Product storage error
Symptomtext
Vaccine may have been stored under condition that departed from the manufacturer's recommended specification, so the manufacturer deem vaccine not viable and recommends a repeat dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- not indicated
- Vorgeschichte
- not indicated
- Andere Medikamente
- none indicated
- Allergien
- not indicated
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 26.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine might have been stored under condition that departed from the manufacturer's recommended specification, so vaccine was deem not viable, so additional vaccine was recommended for patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NOT INDICATED
- Vorgeschichte
- NOT INDICATED
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 25.03.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
PATIENT IS 11 YEARS OLD AND RECIEVED THE VACCINE INTENDED FOR ADULTS 12 AND OLDER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 22.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 26,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
PATIENT DOES NOT HAVE AN ADVERSE EVENT BOOSTER DOSE WAS ADMINISTERED BEFORE THE RECOMMENDES TIME. SECOND DOSE WAS ADMINISTERED IN 11/11/2021 AND BOOSTER DOSE WAS ADMINISTERTED ON 02/23/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 26,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
PATIENT RECIEVED SECOND DOSE ON 11/12/2021. BOOSTER DOSE WAS ADMINISTERES ON 02/23/2022 AND THE 5 MONTH PERIOD WAS NOT COMPLETED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 22.03.2022
- Impfdatum
- 29.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Symptomtext
lump under his armpit; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 29Jan2022 11:50 (Lot number: FL3209) at the age of 58 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "had the Moderna covid vaccines for his first and second dose/third dose of the Pfizer covid vaccine" (unspecified if ongoing), notes: had the Moderna covid vaccines for his first and second dose/third dose of the Pfizer covid vaccine. There were no concomitant medications. Vaccination history included: Moderna (Dose 1), for COVID-19 Immunization; Moderna (Dose 2), for COVID-19 Immunization, reaction(s): "flu like symptoms". The following information was reported: AXILLARY MASS (non-serious) with onset 31Jan2022, outcome "not recovered", described as "lump under his armpit". No follow-up attempts are possible. No further information is expected. Follow-Up (09Feb2022): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary mass
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Interchange of vaccine products (had the Moderna covid vaccines for his first and second dose/third dose of the Pfizer covid vaccine)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- U
- Eingang
- 22.03.2022
- Impfdatum
- 27.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test
Chest X-ray
Culture urine
Electrocardiogram
Energy increased
SARS-CoV-2 test
Therapeutic response unexpected
Symptomtext
Unexpected therapeutic effect; energy boost; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 27Jan2022 10:30 (Lot number: FL3209) as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: THERAPEUTIC RESPONSE UNEXPECTED (non-serious), outcome "recovered", described as "Unexpected therapeutic effect"; ENERGY INCREASED (non-serious), outcome "recovered", described as "energy boost". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient did not have family medical history relevant to events. It was stated that after the vaccination approximately 25 to 30 minutes later the patient felt a tremendous energy boost and when arrived home maybe 45 minutes after the shot was administered the patient went and shoveled snow off our two driveways and a long sidewalk and didn't break a sweat nor was tired at all. The patient wish to could get second shot earlier. It was amazing. thought you would like to hear that. The patient did not receive prior vaccinations (within 4 weeks). The patient did not have arm pain, no muscle pain, in injection site experienced boost of energy lasted 24 hours (up to 36 hours), came home shoveled after shot, entire drive way/side walk, no fatigue, no heart palpitation and no ill affect from the shot. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220106; Test Name: Blood work; Result Unstructured Data: Test Result:Negative; Comments: All with in range.; Test Date: 20220106; Test Name: X-RAY chest; Result Unstructured Data: Test Result:Negative; Comments: All with in range.; Test Date: 20220106; Test Name: Urine culture; Result Unstructured Data: Test Result:Negative; Comments: All with in range.; Test Date: 20220106; Test Name: EKG TEST; Result Unstructured Data: Test Result:Negative; Comments: All with in range.; Test Date: 20220106; Test Name: Covid test; Result Unstructured Data: Test Result:Negative; Comments: All with in range.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 5,0
- Geschlecht
- M
- Eingang
- 21.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Youth patient received a full adult dose of 30 mcg/0.3ml.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 21.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Youth patient received a full adult dose of 30 mcg/0.3ml.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 7,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Youth patient received a full adult dose of 30 mcg/0.3ml.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 17.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Patient 2 dose original series vaccines were administered 2/2/2022, 2/23/2022. A booster was given erroneously on 3/17/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 19.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 3 DAYS. NO ADVERSE EVENT AT THE TIME OF THIS REPORT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- COPD, ARTHRITIS
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
ADMINISTERED BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
ADMINISTERED BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- 27.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
ADMINISTERED BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
ADMINISTERED BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
ADMINISTERED BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
ADMINISTERED BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
dose was administered 1 day after manufacturer suggested beyond use date by 1 day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
ADMINISTERED BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
ADMINISTERED BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
PFIZER COVID-19 VACCINE WAS ADMINISTERED AFTER THE 30 DAY PERIOD THAT THE VACCINE IS ALLOWED TO BE STORED IN THE REFRIGERATOR. PATIENT DID NOT REPORT ANY ADVERSE EVENT TO THE VACCINE THAT HE RECEIVED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
VACCINE WAS ADMINISTERED AFTER THE 30 DAY PERIOD THAT THE VACCINE IS ALLOWED TO BE STORED IN THE REFRIGERATOR. PATIENT DID NOT REPORT ANY ADVERSE EFFECT TO THE VACCINATION SHE RECEIVED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- SEIZURE DISORDER
- Andere Medikamente
- XCOPRI 50MG XCOPRI 200MG LITHIUM CARBONATE ER 450MG ARIPIPRAZOLE 15MG MIRTAZAPINE 45MG FOLIC ACID 1MG VIMPAT 200MG BRIVIACT 75MG LORAZEPAM 1MG VENLAFAXINE ER 75MG
- Allergien
- NSAID ALLERGRY
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
VACCINE WAS ADMINISTERED AFTER THE 30 DAY PERIOD THAT VACCINE IS ALLOWED TO BE STORED IN THE REFRIGERATOR. PATIENT DOES NOT REPORT EXPERIENCING ANY ADVERSE EFFECT TO THE VACCINATION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HYPOTHYROIDISM
- Andere Medikamente
- AMITRIPTYLINE 10MG LEVOTHYROXINE 25MCG
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Received a lot that was possible that it was outside storage limits
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 2 DAYS. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 2 DAYS. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 1 DAY. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 1 DAY. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 2 DAYS. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 2 DAYS. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 1 DAY. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- U
- Eingang
- 17.03.2022
- Impfdatum
- 19.12.1964
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 1 DAY. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- HTN
- Vorgeschichte
- NONE
- Andere Medikamente
- LOSARTAN-HCTZ 50/12.5MG
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 1 DAY. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 1 DAY. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- HTN
- Vorgeschichte
- NONE
- Andere Medikamente
- LOSARTAN/HCTZ 50/12.5MG DAILY
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 1 DAY. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 1 DAY. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 1 DAY. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- U
- Eingang
- 17.03.2022
- Impfdatum
- 11.08.1994
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PATIENT IS INFORMED THE PFIZER GIVEN WAS EXPIRED BY 1 DAY. NO ADVERSE EVENT AT THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oedema peripheral
SARS-CoV-2 test
Swelling
Symptomtext
swollen left armpit; swollen left FOREARM; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 66 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 04Jan2022 10:45 (Lot number: FL3209) as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER0732, Location of injection: Arm Left, Vaccine Administration Time: 03:15 PM), administration date: 25Mar2021, for COVID-19 immunization, reaction(s): "Inappropriate schedule of vaccine administered"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EM9809, Location of injection: Arm Left, Vaccine Administration Time: 05:30 PM), administration date: 02Feb2021, for COVID-19 immunization. The following information was reported: SWELLING (non-serious) with onset 05Jan2022, outcome "recovered", described as "swollen left armpit"; OEDEMA PERIPHERAL (non-serious) with onset 05Jan2022, outcome "not recovered", described as "swollen left FOREARM". The events "swollen left armpit" and "swollen left forearm" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of swelling, oedema peripheral. Additional information No other vaccine in four weeks, No Other vaccine in two weeks. No covid prior vaccination. The swollen armpit subsided, the left forearm has not even after 40 days since the covid booster. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oedema peripheral
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220116; Test Name: home test kit; Test Result: Negative; Comments: Nasal Swab.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History:Patient Other Relevant History 1: none.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 16.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PT WAS GIVEN PFIZER SHOT EXPIRED BY 2 DAYS. NO ADVERSE EVENT BY THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PT WAS GIVEN PFIZER SHOT EXPIRED BY 2 DAYS. NO ADVERSE EVENT BY THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 16.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PT WAS GIVEN PFIZER SHOT EXPIRED BY 2 DAYS. NO ADVERSE EVENT BY THE TIME OF THIS REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PT WAS GIVEN PFIZER SHOT EXPIRED BY 1 DAY. NO ADVERSE REACTION AT THE TIME OF REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE.
- Vorgeschichte
- NONE.
- Andere Medikamente
- NONE.
- Allergien
- NKA.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- U
- Eingang
- 16.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
PFIZER SHOT GIVEN WAS EXPIRED 1 DAY BUT PATIENT HAS NO ADVERSE REACTION AT THE TIME OF REPORT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administration error
Symptomtext
Incident occurred from possible inviable dose administered to patient. We tried to reach the patient 3 times but no answer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administration error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Symptomtext
Incident occurred from possible inviable dose administered to the patient. We tried to reach the patient 3 times but no answer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Symptomtext
Incident occurred from possible inviable dose administered to the patient. We tried to reach the patient 3 times but no answer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Symptomtext
Incident occurred from possible inviable dose administered to the patient. We tried to reach the patient 3 times but no answer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Incident occurred from possible inviable dose being administered to patient. We tried to reach the patient 3 times but no answer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -