- Staat
- MI
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 24.03.2023
- Impfdatum
- 28.07.2022
- Beginn
- 15.03.2023
- Tage bis Beginn
- 230,0
- Dosis
- 1
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Acute respiratory failure
Aortic stenosis
Barrett's oesophagus
Bile duct stone
Biliary dilatation
Biliary sphincterotomy
Blood potassium decreased
COVID-19
Cholecystectomy
Cholelithotomy
Computerised tomogram abdomen abnormal
Echocardiogram abnormal
Encephalopathy
Endoscopic retrograde cholangiopancreatography
Endotracheal intubation
Gallbladder disorder
Hiatus hernia
Symptomtext
Discharge summary: "Brief Summary of Hospital Stay: patient is a 74 YO female a past medical history of hypertension, hyperlipidemia, who presented to the emergency department with acute onset of nausea, vomiting, and RUQ abdominal pain shortly after meal. On arrival, the patient was hemodynamically stable but she was found to have elevated LFTs with cholestatic pattern as well as potassium 2.6. CT abdomen and pelvis was obtained which showed gallbladder and cystic duct distention, mild intrahepatic and extrahepatic biliary dilatation, radiographic findings suggestive of choledocholithiasis. Gastroenterology was consulted who recommended ERCP. Potassium was replaced. The patient initially underwent EGD given limited anesthesia availability, which was negative for Zenker's diverticulum, but did show esophageal mucosa consistent with short-segment Barrett's esophagus as well as a large hiatal hernia, otherwise unrevealing. Patient then underwent ERCP on 3/17/2023 with Dr., where biliary sphincterotomy was performed, the common bile duct was dilated, the biliary tree was swept, and choledocholithiasis was visualized and removed. Patient tolerated the procedure well. General surgery was consulted for cholecystectomy evaluation given her presentation. She underwent robotic assisted laparoscopic cholecystectomy on 3/18/2023 with another Dr. which she tolerated without immediate complicatinon. In the interim, she was receiving maintenance IV fluids. She initially tolerated the surgery well. However, postoperatively on 3/18, she began exhibiting acute encephalopathy and respiratory distress, becoming acutely hypoxic. Attempt was made to place her on BiPAP, however she acutely developed nausea and vomiting. Given her respiratory distress and aspiration risk, ICU was consulted and the patient was intubated for airway protection. The patient was diuresed and started on antibiotics given concern for aspiration pneumonia. She would improvement in her oxygen requirements and was able to be extubated on 3/19 without postextubation complication. She was transferred to floor status. Antibiotics were discontinued given low suspicion for aspiration pneumonia. Suspect that her acute respiratory decompensation was due to volume overload in setting of perioperative IV fluids and is supported chest imaging and physical exam. Echo was obtained which showed EF 50% and mild aortic stenosis and mild-moderate MR. Diuresis was continued, after which the patient demonstrated improvement in her oxygen requirements and respiratory effort, being able to wean down to room air this admission. She had resolution of her abdominal pain in her liver function testing had normalized, she otherwise remained hemodynamically stable. Patient will be discharged home with PRN Lasix to treat volume overload with close PCP follow-up. Patient will follow-up with General surgery. She was discharged home in good condition."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 7,0
- Labordaten
- COVID PCR positive test on 3/18/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 18.08.2021
- Beginn
- 27.02.2022
- Tage bis Beginn
- 193,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
Symptomtext
Person passed away after being diagnosed with COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 24.07.2021
- Beginn
- 22.01.2022
- Tage bis Beginn
- 182,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
SARS-CoV-2 test positive
Symptomtext
Fully vaccinated with Covid vaccine x 2. Tested positive for Covid on 01/22/2022. Admitted to the Hospital in on 01/27/2022. Expired on 02/01/2022 while still hospitalized.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 01.07.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 168,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Myocardial infarction
Symptomtext
Hospital claimed it was a heart attack. But no signs of a heart attack, no past history of hypertension or smoking. Taken by EMTs to hospital, formally admitted, died within minutes of being admitted to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- None - no autopsy was ever done
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Cellebrex 200 mg, Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 09.01.2022
- Impfdatum
- 25.06.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 196,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Antimicrobial susceptibility test resistant
Atelectasis
COVID-19
Cerebrovascular accident
Chest X-ray abnormal
Confusional state
Cough
Culture urine positive
Escherichia infection
Escherichia test positive
Pathogen resistance
Pleural effusion
SARS-CoV-2 test positive
Transient ischaemic attack
Vaccine breakthrough infection
Symptomtext
Covid19 breakthrough. 1st Vaccine received on 05/28/2021. 76 y/o with PMHx of Afib, HTN, CAD, HF, AAA, HLD, BPH was recently discharged on 01/04/2022 for TIA vs CVA found to have Ecoli ESBL Urine. (covid not tested that admission) Now readmitted where family states pt more confused than usual and c/o cough. O2 sats room air 97%, CXR with trace bilat effusions and adjacent atelectasis. Urine culture + again for ESBL Ecoli. Started on IV Abx.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- SARS CoV 2 PCR Covid19 detected on 1/7/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- AFIB, AAA, HTN, HLD, CAD, Parkinson's, HF
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 25.12.2021
- Impfdatum
- 29.06.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Sudden death
Symptomtext
Patient suddenly died 4 weeks after the second dose of Moderna vaccine administration on July 27, 2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sudden death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- hypothyroidism
- Vorgeschichte
- hypothyroidism
- Andere Medikamente
- Synthroid
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 04.09.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Last known alive on the date of vaccination (September 4). Found dead and decomposing in his residence on September 7.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Seizure disorder
- Vorgeschichte
- Seizure disorder
- Andere Medikamente
- Tegretol
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 26.06.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alcohol use
Asthenia
Blood alcohol increased
Brain herniation
Brain injury
Computerised tomogram head abnormal
Death
Fall
Injury
International normalised ratio normal
Pneumocephalus
Prothrombin time normal
Skull fracture
Subdural haematoma
Symptomtext
Fall down stairs, +EtOH, catastrophic brain injury, death. Though her death seems to be clearly caused by direct head trauma, the cause of her fall may be multifactorial including weakness from recent vaccination in combination with EtOH.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 2,0
- Labordaten
- 7/2/21 - EtOH: 340 , PT: 11.9, INR: 1.1 , Head CT: Large R holohemispheric SDH, L subfalcine herniation and effacement of the basal cisterns, L cerebellar intraparenchymal hematoma, L temporal bone fx, pneumocephalus.
- Aktuelle Erkrankungen
- Unk/none
- Vorgeschichte
- Hx SDH and TBI
- Andere Medikamente
- Amlodipine
- Allergien
- Penicillin, egg
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 10.09.2021
- Impfdatum
- 13.06.2021
- Beginn
- 05.07.2021
- Tage bis Beginn
- 22,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Atrioventricular block complete
Coronary artery stenosis
Myocardial infarction
Dizziness
Vertigo
Symptomtext
07/05/21 i had a massive heart attack rca 100 percent blocked i died twice that nite
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 3,0
- Labordaten
- hospital
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 22.07.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Asthenia
Chills
Confusional state
Discomfort
Feeling abnormal
Feeling of body temperature change
Illness
Nausea
Pneumonia
Pulmonary embolism
Pyrexia
Thinking abnormal
Thrombosis
Tremor
Symptomtext
diagnosed with pulmonary embolisms/both lungs collapsed; Blood Clots; Felt smashed; Felt hot and cold; Mind confusion; Sick all over; Nausea; Body discomfort; Felt like fever; Chills; Extreme shaking; Completely weak/ bones felt shattered; Could't think straight; pneumonia; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 19-Aug-2021 and was forwarded to Moderna on 19-Aug-2021. This spontaneous case was reported by a consumer and describes the occurrence of PULMONARY EMBOLISM (diagnosed with pulmonary embolisms/both lungs collapsed), THROMBOSIS (Blood Clots), PNEUMONIA (pneumonia), CONFUSIONAL STATE (Mind confusion), ILLNESS (Sick all over), DISCOMFORT (Body discomfort), PYREXIA (Felt like fever), CHILLS (Chills), TREMOR (Extreme shaking), ASTHENIA (Completely weak/ bones felt shattered), THINKING ABNORMAL (Could't think straight), FEELING ABNORMAL (Felt smashed) and FEELING OF BODY TEMPERATURE CHANGE (Felt hot and cold) in a 56-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Jul-2021, the patient experienced ILLNESS (Sick all over) (seriousness criteria hospitalization and disability), DISCOMFORT (Body discomfort) (seriousness criteria hospitalization and disability), PYREXIA (Felt like fever) (seriousness criteria hospitalization and disability), CHILLS (Chills) (seriousness criteria hospitalization and disability), TREMOR (Extreme shaking) (seriousness criteria hospitalization and disability), ASTHENIA (Completely weak/ bones felt shattered) (seriousness criteria hospitalization and disability) and THINKING ABNORMAL (Could't think straight) (seriousness criteria hospitalization and disability). On 23-Jul-2021, the patient experienced CONFUSIONAL STATE (Mind confusion) (seriousness criteria hospitalization and disability), FEELING ABNORMAL (Felt smashed) (seriousness criteria hospitalization and disability) and FEELING OF BODY TEMPERATURE CHANGE (Felt hot and cold) (seriousness criteria hospitalization and disability). On an unknown date, the patient experienced PULMONARY EMBOLISM (diagnosed with pulmonary embolisms/both lungs collapsed) (seriousness criteria hospitalization, disability and medically significant), THROMBOSIS (Blood Clots) (seriousness criteria hospitalization, disability and medically significant) and PNEUMONIA (pneumonia) (seriousness criteria hospitalization, disability and medically significant). At the time of the report, PULMONARY EMBOLISM (diagnosed with pulmonary embolisms/both lungs collapsed), THROMBOSIS (Blood Clots), PNEUMONIA (pneumonia), CONFUSIONAL STATE (Mind confusion), ILLNESS (Sick all over), DISCOMFORT (Body discomfort), PYREXIA (Felt like fever), CHILLS (Chills), TREMOR (Extreme shaking), ASTHENIA (Completely weak/ bones felt shattered), THINKING ABNORMAL (Could't think straight), FEELING ABNORMAL (Felt smashed) and FEELING OF BODY TEMPERATURE CHANGE (Felt hot and cold) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Patient stated that she continued to experience these side effects as well as feeling smashed, felt heat, felt cold, felt weird, mind confusion and no strength. patient was eventually transported and admitted to the Hospital. The patient remained admitted for 5 days and was diagnosed with pulmonary embolisms, both lungs collapsed, blood clots in lungs and pneumonia. Patient stated that received treatment and was eventually discharged. No concomitant medications was provided.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 16.12.2023
- Impfdatum
- 18.05.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 44,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Biopsy skin abnormal
Blood test
Burning sensation
Chest discomfort
Disability
Dizziness
Electric shock sensation
Formication
Groin pain
Head discomfort
Headache
Joint noise
Magnetic resonance imaging head
Magnetic resonance imaging spinal
Muscle spasms
Muscle twitching
Symptomtext
From july 2021 to April 2022, symptoms were sporadic and intermittent. Symptoms include: patchy itchy skin in cheeks and groin, shooting pain from left knee down the leg, sensation of pulling muscles in the groin, itchy groin and random electric pain all over my body. In April 2022, I had an acute onset of persistent non resolving neurological symptoms. They include: paresthesia all over body and face, pins and needles, tingling, abnormal sensations like burning, skin crawling on face, scalp and genitals, stabbing pain, muscle twitching- spasms allover body, chest discomfort and pain and left ribs pain, spine burning sensation, shoulders-knee-gluteus nerve pain, sharp nerve pain in palm of hands and feet, left knee pain, head pressure, back-headache, hitching, dizzy, lightheaded, groin pain shocks, cracking joints, face rash, middle back pain. Treatment included a taper of prednisone, Lyrica, LDN, vit b12, vit d3, magnesium. Symptoms are still present and are debilitating.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- MRI Brain, Cervical and thoracic spine - inconclusive (march 2021) Autoimmune and neurologic blood work - inconclusive (from march 2021 to present) skin biopsy - positive for sensory SFN (december 2022)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Before or after vaccination? If before, none. If after vaccination, I have been diagnosed with small fiber neuropathy, proctitis and EDS.
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 01.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Hyperhidrosis
Pain
Syncope
Symptomtext
then day of the shot patient had chills, sweats, body aches, and fainted. Symptoms resolved the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 05.11.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 31,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Dizziness
Headache
Illness
Injection site pain
Nausea
Presyncope
Pyrexia
SARS-CoV-2 test negative
Syncope
Symptomtext
Injection site soreness, lethargy for 2 days after injection then no issues until a month later when illness with headache, fever to 101 F, nausea for 2 days and diarrhea for 4 days. Lightheaded with vaso-vagal reaction and fainted on Day 2. No long-term sequelae.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- COVID-19 PCR neg 12/8/22
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- obesity
- Andere Medikamente
- Mature MVI, Vit D3, Sertraline, docusate sodium
- Allergien
- Thiomersal, sulfa
- Vorherige Impfungen
- 1970's tetanus - arm locked in elevated position for days - possibly related to thiomersal allergy that developed to contact len
- Staat
- -
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 30.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Lipids
Pain in extremity
Peripheral swelling
Superficial vein thrombosis
Ultrasound Doppler
Symptomtext
Patient sent an email on 11/29/2021 to report that he has been diagnosed with a superficial thrombophlebitis, after several days of painful swelling on the lower leg.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Superficial vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Blood tests:Lipid panel; Doppler.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- NONE
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 25.10.2021
- Impfdatum
- 09.07.2021
- Beginn
- 10.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Dyspnoea
Echocardiogram
Electrocardiogram
Palpitations
Presyncope
Sensory disturbance
Symptomtext
Sudden onset of pounding heart, buzzing sensation throughout body, near blackouts, and shortness of breath. Buzzing sensation and near blackouts have subsided during past two weeks, but pounding heart and shortness of breath continue on a constant basis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- Various bloodwork, multiple EKGs, and an echocardiogram.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 23.09.2021
- Impfdatum
- 30.06.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 13,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Balance disorder
Blood test
Computerised tomogram
Dizziness
Electrocardiogram
Eye movement disorder
Nausea
Syncope
Tremor
Vertigo
Symptomtext
Extreme Dizziness, Vertigo, Syncope, Unsteadiness, Bouncy vision Nystagmus, Nausea, Shakiness Balance issues weakness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- CT Scan EKG Blood tests Medication therapies PT ENT Consult and Audiogram to follow Neuro consult to follow
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 22.09.2021
- Impfdatum
- 01.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electric shock sensation
Pain assessment
Product dose omission issue
Trigeminal neuralgia
Symptomtext
She was one week past the second dose due date; Electrical shocks on the right side of her face; Trigeminal neuralgia became bilateral; Trigeminal neuralgia flare up; This spontaneous case was reported by a consumer and describes the occurrence of PRODUCT DOSE OMISSION ISSUE (She was one week past the second dose due date), ELECTRIC SHOCK SENSATION (Electrical shocks on the right side of her face), TRIGEMINAL NEURALGIA (Trigeminal neuralgia flare up) and TRIGEMINAL NEURALGIA (Trigeminal neuralgia became bilateral) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The patient's past medical history included Lumbar strain, Neurostimulator implantation (For Lumbar issue) and Microvascular decompression (2 failed surgeries for Trigeminal neuralgia) from May 2019 to December 2020. Concurrent medical conditions included Trigeminal neuralgia (Left side) since 2019 and Chronic kidney disease (Stage 3b) since 2008. Concomitant products included CARBAMAZEPINE (TEGRETOL), TRAMADOL and CARBAMAZEPINE from 01-Sep-2019 to an unknown date for Trigeminal neuralgia. On 01-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Jul-2021, the patient experienced TRIGEMINAL NEURALGIA (Trigeminal neuralgia flare up). On 19-Jul-2021, the patient experienced ELECTRIC SHOCK SENSATION (Electrical shocks on the right side of her face) and TRIGEMINAL NEURALGIA (Trigeminal neuralgia became bilateral). On 05-Aug-2021, the patient experienced PRODUCT DOSE OMISSION ISSUE (She was one week past the second dose due date). On 08-Jul-2021, TRIGEMINAL NEURALGIA (Trigeminal neuralgia flare up) had resolved. At the time of the report, PRODUCT DOSE OMISSION ISSUE (She was one week past the second dose due date) had resolved, ELECTRIC SHOCK SENSATION (Electrical shocks on the right side of her face) outcome was unknown and TRIGEMINAL NEURALGIA (Trigeminal neuralgia became bilateral) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Pain assessment: 10/10 (High) 10/10. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medication reported also include cold medicine occasionally for the trigeminal neuralgia. The patient consulted a new neurologist and was about to start new medications. This case was linked to MOD-2021-319322 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 13-Sep-2021: Patient details, Medical history, Lab data, Concomitant medication and Event updated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- Test Name: Pain Scale; Result Unstructured Data: 10/10
- Aktuelle Erkrankungen
- Chronic kidney disease (Stage 3b); Trigeminal neuralgia (Left side)
- Vorgeschichte
- Medical History/Concurrent Conditions: Lumbar strain; Microvascular decompression (2 failed surgeries for Trigeminal neuralgia); Neurostimulator implantation (For Lumbar issue)
- Andere Medikamente
- TEGRETOL; TRAMADOL; CARBAMAZEPINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 20.09.2021
- Impfdatum
- 15.09.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Seizure
Symptomtext
PATIENT'S FATHER REPORTS SEVERAL HOURS AFTER VACCINE PATIENT HAD A SEIZURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- BIRTH CONTROL
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 07.09.2021
- Impfdatum
- 29.07.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
C-reactive protein increased
Chest discomfort
Echocardiogram
Electrocardiogram
Electrocardiogram ambulatory
Magnetic resonance imaging thoracic abnormal
Myocarditis
Pain in jaw
Red blood cell sedimentation rate increased
Troponin
Symptomtext
I was hospitalized for myocarditis. It started Sunday 8/1 with chest tightness and then pain under my jaw. I went in Monday morning to the ER and was hospitalized for 3 days. I was diagnosed with myocarditis related to the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 3,0
- Labordaten
- Troponin level of 3.2 when I went to the ER (8/2), MRI on 8/2 which revealed inflammation in the myocardium. Elevated CRP, elevated ESR levels. I also received an echo, EKG, and was attached to a holter monitor.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Daily multivitamin and birth control pill
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 31.08.2021
- Impfdatum
- 04.08.2021
- Beginn
- 04.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anxiety
Hyperhidrosis
Hypotension
Loss of consciousness
Syncope
Symptomtext
Patient was ready to leave after the required 15-minute wait time post-vaccination; however, when he stood up, he fainted. He regained consciousness immediately after healthcare providers came to his aid. He was diaphoretic and stated he didn't realize he had fainted. His blood pressure was very low and we gave him a bottle of water to drink and called the paramedics. After he was evaluated, he decided not to go to the ER and was picked up by a family member. After seeing him recently, he stated that the incident occurred because he had not eaten very much before getting the vaccine in addition to being anxious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 13.06.2021
- Beginn
- 14.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysarthria
Hemiplegia
Ischaemic stroke
Symptomtext
Patient developed a large vessel occlusion (ischemic stroke) within 24 hours of receiving the first dose of the Moderna vaccine. Stroke is cryptogenic in etiology, with consideration of hypercoagulability of malignancy as possible etiology
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- renal cell Ca
- Vorgeschichte
- as above
- Andere Medikamente
- metoprolol, lisinopril, clonazepam, wellbutrin
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 01.08.2021
- Impfdatum
- 01.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Hyperhidrosis
Loss of consciousness
Nausea
Pallor
Symptomtext
The patient's wife was with him while he was waiting the 15 minutes. She stated that he was feeling nauseous and dizzy. When I went to check on him, he was sloughed over to the right side of his chair with his eye closed. The wife tried to talk to him, but he was unresponsive for a little while. When he came back to responding, he was sweaty and said that he felt like he went to sleep. I had one of my technicians call 911. His wife believes that he had a seizure. He was sweaty and pale. The EMT ended up taking him to go to the hospital to get checked out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- Patient that he does not take take any medications or over the counter supplements/medications
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 30.07.2021
- Impfdatum
- 30.07.2021
- Beginn
- 30.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nervousness
Syncope
Symptomtext
Patient felt shaky and fainted but still remain conscious. I ran out to put patient on the floor and monitor her condition closely. i kept asking her if she has trouble of breathing and she said that she's OK while my tech had already called the 911 for help. 5 minutes later the paramedic arrived and performed vital checks on her. they said she's ok nothing wrong with her so she doesn't need to go to the hospital for any further check up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- healthy not sick at the time of vaccination
- Vorgeschichte
- no
- Andere Medikamente
- none
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 28.07.2021
- Impfdatum
- 10.07.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood test
Computerised tomogram
Dyspnoea
Electrocardiogram
Palpitations
Pericarditis
Sensory disturbance
Symptomtext
Pt. states that after receiving the 2nd dose of Moderna 07/10/2021, started experiencing symptoms 07/13/2021 of shortness of breath, heart palpations, weakness, and throbbing through the back. ER visit 07/17th,20th, 23rd/2021, acute-pericarditis sent home with 600mg Ibuprofen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- Blood Test 07/23/2021 Cat Scan 07/23/2021 EKG 07/23/2021
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 27.07.2021
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
patient fainted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 26.07.2021
- Impfdatum
- 26.07.2021
- Beginn
- 26.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
General physical condition abnormal
Loss of consciousness
Symptomtext
Patient sat outside of pharmacy in a chair for approximately 5 minutes. He started to look not so well. Went to bring him back into consultation room and he passed out. He laid down on the floor for 10 minutes or so. Gave him some water and animal crackers.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 23.07.2021
- Impfdatum
- 22.07.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Hyperhidrosis
Hypotension
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Hypotension-Mild, Additional Details: pt fainted after receiving second dose of vaccine; lack of food in stomach plus cannabis inhalation earlier in the morning
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 22.07.2021
- Impfdatum
- 21.07.2021
- Beginn
- 21.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Refusal of treatment by patient
Syncope
Vomiting
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Systemic: Vomiting-Mild, Additional Details: Patient fainted after a few minutes of receiving 2nd covid vaccine in the waiting area. Patient did regain consiousness within a minute and in few minutes patient started vomiting. Patient refused call for emergency medical attention and states she has fainted before. Patient was monitored for 30 minutes before leaving with younger brother and boyfriend. She stated she felt okay before leaving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 21.07.2021
- Impfdatum
- 21.07.2021
- Beginn
- 21.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Dyspnoea
Pallor
Presyncope
Symptomtext
PT FELT OUT OF BREATH AND EXPERIENCING DIZZINESS. FACE WAS PALE. NOTICED THAT THE PT WAS ABOUT TO EXPERIENCE SYNCOPE, I TOLD HER TO LIE DOWN WITH HER FEET ELEVATED. AFTER 5 MINUTES, PT'S SYMPTOMS WERE RELIEVED AND DRANK WATER AND SAT FOR 15 MINUTES AFTERWARDS WHILE BEING MONITORED. NO FOLLOW UP WAS REQUIRED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- MODERNA COVID VACCINE
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 18.07.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Brain scan abnormal
Central nervous system lesion
Condition aggravated
Electrocardiogram ambulatory
Electroencephalogram
Seizure
Transient ischaemic attack
Symptomtext
Day after the vaccine she had a seizure or mini stroke that lasted between 35 minutes and 1 hour. She is currently being tested. This was her second seizure if it was a seizure. The other one occurred almost a month previously. She saw a Dr. who said it could possibly be a side effect of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- EEG, heart monitor, seeing a neurologist on 7/30/21
- Aktuelle Erkrankungen
- Had a seizure on 5/15 that lasted 5 to 10 minutes. After that no other seizures. Had the vaccine on 6/11/21 and had either a seizure or mini stroke the following day. It lasted 35 minutes to 1 hour. On imaging they found a lesion on her brain where seizures are activated. She's going through testing - wearing a heart monitor and EEG
- Vorgeschichte
- -
- Andere Medikamente
- Aspirin 81mg, Levetiracetem 500mg, rosuvastatin 20mg, lisinopril/hctz 20/25mg, carvedilol 25mg
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 14.07.2021
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Chills
Dizziness
Feeling hot
Influenza like illness
Injection site pain
Muscle spasms
Pain
Pyrexia
Thrombosis
Symptomtext
Patient received first Moderna dose on June 8, 2021 and second dose on July 6, 2021. Patient started having flu-like symptoms such as, Fever (but doesn't know what temperature as she did not measure but she felt hot) and chills. After 1-2 days of flu-like symptoms she began to have painfulness around the left arm where she received both of her Moderna vaccines. This painfulness started 3-4 days after receiving the 2nd dose of Moderna vaccine. Patient was also having symptoms of pinching, aches, cramps on left arm along with light-headedness and dizziness. Patient visited the Emergency Department on July 12, 202 and confirmed by the Doctor that there is a blood clot on the left arm. The doctor at the Emergency Department wanted patient to reach out to the pharmacy and report the incident. Patient is currently prescribed for a blood thinner and will follow up with doctors tomorrow 07/15/2021 and another doctor in a week. Patient has allergies to Tree nuts and citrus seeds and was on a birth control Estarylla 0.25-0.035mg tablets until the day she found out that she has a blood clot (07/12/2021).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- Per patient, she is on a birth control (Estarylla 0.25-0.035mg Tablets). But stopped on the day visit to the ER on 07/12/2021 after finding out that she has a blood clot.
- Allergien
- Tree nuts, Citrus seeds
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 13.07.2021
- Impfdatum
- 13.07.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Loss of consciousness
Symptomtext
Approximately 5 minutes after receiving the Moderna vaccine, dose 2, the patient appeared to lose consciousness. Patient was seated in chair at the time and was with her sister. The sister held on to her so that she would not fall over (patient dropped cell phone on floor). About a minute or so later, the patient appeared to be conscious again and was resting in the waiting area of the pharmacy. At first the patient appeared confused and unaware of what was going on. Patient was given a bottle of water and paramedics were called. Paramedics arrived about 10 minutes later, checked all vitals and talked to the patient. Vitals appeared fine and no abnormalities noted. Paramedics then left and the pharmacist interviewed the patient, who by this time was aware and responsive. She indicated that she fainted shortly after receiving the vaccine but felt better after the paramedics left.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- unknown
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 12.07.2021
- Impfdatum
- 21.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Computerised tomogram
Fall
Headache
Heavy menstrual bleeding
Loss of consciousness
Menstrual disorder
Nausea
Vomiting
Symptomtext
threw up a few times; I actually past out that morning; I woke up 5 AM and I was bleeding very heavy; My right side (side I fell on) of the head still hurts; severe headache/ My right side (side I fell on) of the head still hurts; feel nauseous; I got my period days early from my usual; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of LOSS OF CONSCIOUSNESS (I actually past out that morning) in a 42-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Nausea and Pain. Concomitant products included ONDANSETRON (ZOFRAN [ONDANSETRON]) for Nausea, NAPROXEN SODIUM (ALEVE) for Pain. On 21-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Jun-2021, the patient experienced MENSTRUAL DISORDER (I got my period days early from my usual). On 29-Jun-2021, the patient experienced LOSS OF CONSCIOUSNESS (I actually past out that morning) (seriousness criterion medically significant), HEAVY MENSTRUAL BLEEDING (I woke up 5 AM and I was bleeding very heavy), FALL (My right side (side I fell on) of the head still hurts), HEADACHE (severe headache/ My right side (side I fell on) of the head still hurts) and NAUSEA (feel nauseous). On an unknown date, the patient experienced VOMITING (threw up a few times). At the time of the report, LOSS OF CONSCIOUSNESS (I actually past out that morning) was resolving, HEAVY MENSTRUAL BLEEDING (I woke up 5 AM and I was bleeding very heavy), MENSTRUAL DISORDER (I got my period days early from my usual), FALL (My right side (side I fell on) of the head still hurts) and VOMITING (threw up a few times) outcome was unknown and HEADACHE (severe headache/ My right side (side I fell on) of the head still hurts) and NAUSEA (feel nauseous) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, Computerised tomogram: normal (normal) normal. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Patient never had any issues with the menstrual cycle and never had this much blood. Patient went to emergency department and ran a few imaging tests like CT scans and others which were turned out as normal. Treatment medication were not reported. Company Comment: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.Very limited information regarding this event has been provided at this time.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.Very limited information regarding this event has been provided at this time
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: CT scan; Result Unstructured Data: normal
- Aktuelle Erkrankungen
- Nausea; Pain
- Vorgeschichte
- -
- Andere Medikamente
- ZOFRAN [ONDANSETRON]; ALEVE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 11.07.2021
- Impfdatum
- 09.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electric shock sensation
Hypersomnia
Injection site pain
Neuropathy peripheral
Paraesthesia
Symptomtext
After my first Covid 19 shot I started to feel jabs of electrical jabs consistent with neuropathy in various parts of my body. Now, my hands and feet keep getting pins and needles. I keep feeling neuropathy sensations elsewhere as well. I am uncomfortable and have to keep moving to try and get rid of the sensations, but even that doesn't help. I had expected pain in the area where the dose was injected and I slept a lot...... I did NOT expect to experience pins and needles consistent with nueropathy all over, and especially in my hands and feet, that are affecting me almost two days later still. I now have deep reservations about my follow up shot. I am keeping a copy of this report for my records.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Type 2 Diabetes, Metabolic Syndrome, High Blood Pressure
- Andere Medikamente
- Metoprolol .5, Hydrochlorothiazide 25mg, Levothyroxine 137 mcg, Amlodipine 10mg, Esmeprazole , FLonase
- Allergien
- Fluconazole
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 07.07.2021
- Impfdatum
- 07.07.2021
- Beginn
- 07.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Nervousness
Pain
Peripheral coldness
Presyncope
Symptomtext
Patient was very nervous about getting vaccine - she reported having rare side effects often ... she reported that about 2 minutes felt faint and dizzy and"pre-syncope ", about 10 minutes later felt legs were cold and body aches... Pt sat for 30 minutes and called a friend . .. she felt well enough to drive home with her friend following her ... the entire time patient was alert and was able to hold conversation Pt has an appointment with her doctor tomorrow morning already planned prior to receiving vaccine so she will follow up
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 06.07.2021
- Impfdatum
- 01.07.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Extra dose administered
Hospitalisation
Syncope
Symptomtext
A FAMILY MEMBER OF PATIENT WITH RX# 7006047-1041, CAME OVER STATING THAT WE GAVE PATIENT A 3RD MODERNA SHOT. SHE STATED THE VACCINE CARD ALREADY REFLECTED 2 SHOTS WHICH SHE VERIFIED WITH DOCTOR (THERE WAS ONLY ONE LOT NUMBER) AND WE GAVE HIM A THIRD ONE. PATIENT CAME IN ON 7/1/2021 AS A WALK IN AND REQUESTED HIS SECOND SHOT. PATIENT FILLED CONSENT FORM AND SHOT WAS BILLED AS 2ND SHOT VIA MEDICAID, FL SHOTS WAS VERIFIED AND ONLY SHOWED ONE SHOT, AND WE ASKED PATIENT "IS THIS YOUR FIRST SHOT OR SECOND SHOT?" AS IS OUR STANDARD PROCESS. Family member claims pt had dizziness and fainting resulting in hospitalization.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hospitalisation
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown - fills at Pharmacy
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 05.07.2021
- Impfdatum
- 01.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fall
Loss of consciousness
Refusal of treatment by patient
Symptomtext
Patient felt light headed and passed out which led to falling down on the ground 2-3 minutes after receiving the first dose of the Moderna vaccine. Patient with supported to the ground until EMT showed up and assessed the reaction. The patient felt okay minutes later and refused to go to the hospital with the EMTs.
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
- Penicillin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 03.07.2021
- Impfdatum
- 02.07.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Syncope
Symptomtext
Patient fainted after vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 01.07.2021
- Impfdatum
- 01.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaphylactic reaction
Extremity contracture
Fall
Hypotension
Seizure
Unresponsive to stimuli
Wheezing
Symptomtext
Following administration of the vaccine, the patient and his wife were seated and I requested they remain seated for 15 min after because I had recently had someone with a fear of needles collapse after their shot, at which point I had already counseled on the things to expect afterward but the patient stopped responding and slumped over. I was unsure if he was breathing as his wife was cradling his head, so I shouted for a technician to call 911. I heard a sound that I perceived to be wheezing and administered an epipen at which point the patients limbs began to contract so I then suspected it was a seizure. We lowered the patient to the ground and shortly after he became responsive. He was able to state his name and date of birth and breathing was unlabored. Pulse ox was 98 and HR was 88 BPM before EMS arrived. They examined the patient and determined it was "anxiety induced response" but also noted that the bloodpressure was "very low" which is consistent with anaphylaxis, but I did not examine the patient at that time. He was sent home afterward.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- 88 BPM (heart rate) 98% O2 saturation (measured via OTC pulse ox machine)
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Penicillin & Sulfa antibiotics
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 28.06.2021
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Hyperhidrosis
Loss of consciousness
Tremor
Symptomtext
Patient passed out, fell to floor, got up in sweats, shaking. Patient was given water, orange juice, BP taken, BP rose with second reading, called paramedics, patient was checked out by EMS and was ok after 30 or so minutes. patient was able to go home by himself.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- erythromycin, morphine
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 26.06.2021
- Impfdatum
- 26.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fall
Head injury
Nausea
Syncope
Symptomtext
Patient fainted approximately 15 minutes after administration. He felt nauseated immediately before, then fainted, falling to the floor and striking his head.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 25.06.2021
- Impfdatum
- 25.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose
Loss of consciousness
Memory impairment
Seizure
Symptomtext
After receiving second dose of vaccine, patient had a seizure within 5 minutes or so. Pharmacist placed patient on the floor on her side. After a minute or so, patient was conscious and was able to state her name and basic information. She did not remember seizing and has no history of seizures.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Paramedics came and took basic vitals - blood pressure, glucose, etc.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 24.06.2021
- Impfdatum
- 24.06.2021
- Beginn
- 24.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fall
Head injury
Loss of consciousness
Skin laceration
Symptomtext
Patient experienced light-headedness minutes after receiving the vaccine during her 15 minute observation period - she briefly lost consciousness and fell out of her seat, striking her head on product shelving. She exhibited two minor lacerations approximately one inch long on her right arm and the right side of her face. She regained consciousness immediately and was fully aware of her surroundings. Patient received first aid treatment with antiseptic solution, antibiotic ointment, and bandages.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 23.06.2021
- Impfdatum
- 23.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaphylactic reaction
Dyspnoea
Unresponsive to stimuli
Symptomtext
Patient came to get his first dose of Moderna vaccine, and anaphylaxis happens after 3-4 minutes. Patient seems to gasp for breath. He did not respond to call/touch. Pharmacist ran out to give EpiPen, then laid patient down onto the floor with his legs up onto the chair while the tech called 911. EMS came and took it over. Patient however denied to go to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 23.06.2021
- Impfdatum
- 21.06.2021
- Beginn
- 21.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram
C-reactive protein
Chest X-ray normal
Chills
Computerised tomogram head
Dizziness
Dyspnoea
Electroencephalogram
Full blood count
Headache
Intensive care
Laboratory test
Magnetic resonance imaging
Palpitations
Paraesthesia
Procalcitonin
Rash
Red blood cell sedimentation rate
Symptomtext
Rec'd Moderna Dose #2 and developed HA, chills and tingling sensation in her fingers. Rash reportedly appeared on her arm. Rec'd Benadryl and rash disappeared. After a nap that day, pt awoke with SOB, palpitations, dizziness, and rash returned on right arm and right neck. Came to ED for evaluation (6/22/21 @ 0514). Tachycardic. In ED, pt's mother noted pt would say something & then repeat what she said seconds later. Dx with seizure in ED and given Ativan 2mg IV. CXR, CT of head, and CTA of chest were all unremarkable. Afebrile, WBC normal, no COVID-19 detected. Pt admitted to ICU for further evaluation and treatment. Also had seizure-like activity during ID MD's exam 6/23/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- -
- Labordaten
- 6/22 to 6/23/21: CXR, CT Head, MRI; CTA Chest; Neuro Consult; Infectious Disease Consult; Cardiology Consult; EEG; Labs (CRP, ESR, COVID testing, CBC, Chem-7, Procalcitonin, etc.)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, seasonal allergies, migraines
- Andere Medikamente
- Ibuprofen, Singulair, Claritin, Albuterol MDI
- Allergien
- Animal Dander; Mold; Peanut
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 23.06.2021
- Impfdatum
- 12.06.2021
- Beginn
- 14.06.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest X-ray
Chest pain
Computerised tomogram
Dyspnoea
Electrocardiogram
Heart rate increased
Hypoaesthesia
Laboratory test abnormal
Platelet count decreased
Rash macular
Syncope
Tinnitus
Symptomtext
Fainted in the car, went to urgent care with chest pains, shortness of breath, trouble breathing (needed oxygen) elevated and rapid heart rate, ringing in ears, numbness in left hand, arm and feet, blotches on arms and legs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- In the hospital I was given 2 ekg?s, labs, cat scan and chest X-ray. All came back normal except low platelet count (133)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 22.06.2021
- Impfdatum
- 21.06.2021
- Beginn
- 21.06.2021
- 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
Muscle spasticity
Symptomtext
Felt light headed. Passed out. Body became rigid. Lasted about 2 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- BP 110/75 HR 79
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 21.06.2021
- Impfdatum
- 21.06.2021
- Beginn
- 21.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Confusional state
Dizziness
Head injury
Hyperhidrosis
Nausea
Paraesthesia
Seizure
Syncope
Symptomtext
Patient was in the lobby area of pharmacy when he passed out. The pharmacy manager tried to talk to the patient, but he appeared to be having a seizure (his eyes were rolled up in his head, he was shaking). When the patient came to he seemed confused about where he was. He began sweating profusely. He said he was nauseated and lightheaded. He said he was tingling all over his body. We also noticed that he was bleeding where he hit his head on the ground when he passed out. He stayed seated while the pharmacy manager held a paper towel to the bleeding part on his head. He sipped some water until the EMS arrived and took over. The patient left to go to the ER with the EMS crew after 3:00PM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- None performed in pharmacy. Patient taken to ER.
- Aktuelle Erkrankungen
- Patient had diverticulitis. Patient said last September, he had a seizure thought to be due to the combination of medications he was taking at the time.
- Vorgeschichte
- Patient denies any chronic or long-standing health conditions.
- Andere Medikamente
- Patient denied taking anything to pharmacy and paramedics.
- Allergien
- patient reported no allergies to pharmacy or paramedics.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 0,3
- Geschlecht
- F
- Eingang
- 21.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Bacterial test negative
Blood glucose normal
Computerised tomogram normal
Electroencephalogram normal
Exposure via breast milk
Lumbar puncture normal
Magnetic resonance imaging normal
Seizure
Viral test negative
Symptomtext
I (mother of patient ) received the first dose of the Moderna vaccine on Friday June 18th at approximately 01:30pm. I fed my three month old daughter milk that I pumped from my breasts later that night and put her to bed. When transferring her to her bassinet at approximately 11:30pm, she started a seizure that lasted seven minutes. We were transported to Hospital where she suffered two more seizures in the early morning hours of June 19th. She has been a healthy baby with no health conditions prior to these events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- 2,0
- Labordaten
- Bacterial/viral tests came back negative June 21 Glucose came back negative June 19 Two EEG tests came back normal. June 19&20 MRI/CT scans came back normal. June 19th Spinal test came back normal. June 21
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 19.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 19.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Syncope
Vomiting
Symptomtext
Lightheaded, dizziness, then proceeded to faint. I was in a sitting position and my boyfriend said I passed out for 5 seconds. I vomited immediately after regaining consciousness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- Psorias flare up
- Vorgeschichte
- Psoriasis
- Andere Medikamente
- Birth control pill
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 18.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Coordination abnormal
Dizziness
Dyspnoea
Hyperhidrosis
Syncope
Unresponsive to stimuli
Symptomtext
Patient became dizzy/loss coordination and collapsed after completing 15 minute observation period. He was able to stand back up and walk to a chair with assistance from family members. At the immediate time of him sitting down after fall, he was unresponsive when asked his name. Approximately 5 minutes after initiation of episode he began to communicate and regain responsiveness but stated he continued to feel dizzy, sweaty, and had some difficulty breathing. At this time EMS arrived on the scene and took over the care of the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 18.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Syncope
Symptomtext
Syncopal episode without injury. Patient briefly lost consciousness, and was placed on the floor on his back with legs elevated, at which point the patient quickly regained consciousness. Patient was advised to remain on the floor and attempt to stand only under supervision of the pharmacist. After approximately twenty minutes the patient was able to stand and walk with no difficulty and was allowed to leave. No signs of injury or trauma were noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Long term tobacco and cannabis user
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 16.06.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Loss of consciousness
Syncope
Symptomtext
RPH asked patient to stay in the store for 15 minutes after he administered her first covid shot, 5 minutes later she passed out in the store, Ambulance was contacted, patient got conscious by the time ambulance came,, they took her to the hospital, been trying to contact her and but she is not answering her phone
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 16.06.2021
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
General physical condition abnormal
Loss of consciousness
Symptomtext
After receiving COVID vaccine, patient was sitting for approximately 5 minutes and then slumped over on top of his clinician. Pharmacist ran out to patient and brought him to the floor to check his breathing. His breathing was steady and he was slowly coming back to consciousness. We immediately called 911 while all of this was happening. Upon questioning patient's clinician said he had been feeling light headed all day. When then the fire department came patient reported to them he had not eaten or drank anything all day. Ambulance came 10 minutes after fire and took him to the hospital for fluids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- lamotrigine
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 15.06.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Presyncope
Syncope
Symptomtext
THE PATIENT WAS FEELING FAINT AND TRIED TO LAY DOWN AND PASSED OUT ON THE WAY TO THE FLOOR. IT WAS A VASOVAGAL RESPONSE. WE HAD HIM LAY ON THE FLOOR FOR ABOUT 10 MINUTES. BP WAS 82/71 PULSE WAS 62. WE GAVE HIM A GATORADE AND A WATER. AFTER 30 MINUTES HE WAS FEELING NORMAL AGAIN. HE REFUSED MEDICAL HELP. HIS EMERGENCY CONTACT WAS NOTIFIED. HE LEFT FEELING FINE AT 2:15PM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- BP 82/71 PULSE 62
- Aktuelle Erkrankungen
- HYPERTENSION
- Vorgeschichte
- -
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 14.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 13.06.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Electrocardiogram normal
Hyperhidrosis
Nausea
Troponin increased
Myocarditis
Vomiting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 06.06.2021
- Impfdatum
- 05.06.2021
- Beginn
- 05.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Loss of consciousness
Syncope
Symptomtext
PATIENT EXPERIENCED SYNCOPE, LOSING CONSCIOUSNESS BRIEFLY. FELL OUT OF CHAIR AND REGAINED CONSCIOUSNESS ROUGHLY 15 SECONDS LATER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 03.06.2021
- Impfdatum
- 03.06.2021
- Beginn
- 03.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Presyncope
Symptomtext
Patient had a typical vasovagal response. She lost conscious for seconds, then regained consciousness. She was slightly dizzy but we had her lay on her back with feet elevated. After 5 minutes she was back to normal. Patient was observed for 20 more minutes with no issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 27.01.2023
- Impfdatum
- 27.01.2022
- Beginn
- 21.12.2022
- Tage bis Beginn
- 328,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anion gap increased
Anxiety
Blood bicarbonate decreased
Blood glucose increased
COVID-19
Condition aggravated
Diabetic ketoacidosis
Dyspnoea
Insulin therapy
Laboratory test abnormal
SARS-CoV-2 test positive
Starvation ketoacidosis
Symptomtext
Patient with history of COVID vaccines who admitted to hospital after COVID detected PCR prior to admit. Provider d/c note: "48 YO male with PMH Bipolar disorder, DM2, HTN, who presents to the hospital with complaint of SOB due to anxiety. Labs with elevated anion gap, elevated blood glucose (200s) and low bicarb. Suspected starvation ketosis vs DKA, patient started on insulin gtt and BMP q4H. With D5 NS Kcl infusion initially. As anion gap closed and bicarb improved, patient switched over to lantus and lispro (titrated to lantus 30 units daily and lispro 10 units three times daily). As patient was taking humalin u500 at home, he was on a carb counting dose; however, suspect that current starvation ketosis likely from use on short acting insulin alone without any long acting coverage. Patient has known gastric lesion which GI was consulted on previous admission, but he has not followed up with recommendation to follow up at gastroenterology. He has severe anxiety and mood disorder that limits his functioning. Psychiatry was consulted during this admission and medications were uptitrated (including vraylar 6mg daily, zoloft 100 mg daily and prn olanzapine for anxiety). Currently, stable for discharge. "
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 8,0
- Labordaten
- Covid PCR Detected 12/17/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension Endocrine Diabetes mellitus, type 2 (HCC) Diabetic peripheral neuropathy (HCC) Psychological Bipolar I disorder with depression (HCC) Panic disorder Generalized anxiety disorder with panic attacks Respiratory Sleep apnea Other Spinal stenosis Dyslipidemia Chronic pain syndrome Environmental allergies Morbid obesity with BMI of 40.0-44.9, adult (HCC) Anxiety Bursitis of right hip Insomnia
- Andere Medikamente
- atorvastatin (LIPITOR) 40 mg tablet Take 1 tablet by mouth daily. busPIRone (BUSPAR) 10 mg tablet Take 2 tablets by mouth 3 (three) times daily. cariprazine (VRAYLAR) 6 mg capsule Take 1 capsule by mouth daily. dicyclomine (BENTYL) 20 mg
- Allergien
- Atarax [Hydroxyzine Hcl]
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 19.01.2023
- Impfdatum
- 16.12.2021
- Beginn
- 07.01.2023
- Tage bis Beginn
- 387,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 1/7/2023 - 1/16/2023 (9 days) Presentation to the ED: SOB. COVID + date: 1/7/23. Treatment: remdesevir and levaquin. Discharge to: home. Moderna 033B21A 5/17/2021 Moderna 051C21A 6/15/2021 Moderna 078J21A 12/16/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CAD, HTN, chronic narcotic use, AS, CHF, COPD.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 10.11.2022
- Impfdatum
- 27.07.2021
- Beginn
- 13.09.2022
- Tage bis Beginn
- 413,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest pain
SARS-CoV-2 test positive
Symptomtext
08/13/22 presents to ED for "chest pain". PMHx of "cigarette smoking, otherwise no medical problems"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 09/13/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 10.11.2022
- Impfdatum
- 27.07.2021
- Beginn
- 13.09.2022
- Tage bis Beginn
- 413,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest pain
SARS-CoV-2 test positive
Symptomtext
08/13/22 presents to ED for "chest pain". PMHx of "cigarette smoking, otherwise no medical problems"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 09/13/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 12.07.2021
- Beginn
- 26.08.2022
- Tage bis Beginn
- 410,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
Nausea
SARS-CoV-2 test positive
Vomiting
Symptomtext
Hospitalization: 8/26/2022 ADMITTED 9/9/2022 DISCHARGED. Presentation to the ED: nausea, vomiting, shortness of breath. COVID-19 + date: 8/26/22. Treatment: WAS NOT GIVEN REMDESIVIR D/T TESTING POSITIVE FOR MORE THAN 2 WEEKS. PATIENT WAS PREVIOUSLY POSITIVE FOR COVID ON 8/11/22 AND WAS ALSO ADMITTED TO THE HOSPITAL THEN. Discharge to: HOME.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 14,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ETOH induced hepatitis, Bipolar depression, DM, HTN, COPD.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 20.09.2022
- Impfdatum
- 11.08.2021
- Beginn
- 11.09.2022
- Tage bis Beginn
- 396,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Abdominal pain
Chest discomfort
Cough
Dyspnoea
Myalgia
COVID-19
SARS-CoV-2 test positive
Nausea
Respiratory tract congestion
Vomiting
Wheezing
Symptomtext
congestion, cough, chest tightness, SOB, wheezing, abdominal pain, nausea, vomiting, myalgias
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 01.06.2021
- Beginn
- 28.08.2022
- Tage bis Beginn
- 453,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
08/27/22 presents to EC ED for "shortness of breath". PMHx of "alcohol abuse"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 08/28/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 10.06.2021
- Beginn
- 12.08.2022
- Tage bis Beginn
- 428,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Cough
Dyspnoea
Fatigue
Hypotension
Malaise
Myalgia
Pyrexia
SARS-CoV-2 test positive
Symptomtext
92 y.o. female with PMHx of CHF, CAD, HTN, hypothyroidism presented to the hospital with 3 days of worsening shortness of breath, fever/chills, myalgias, fatigue, and an intermitted cough. Had not been taking home Lasix since she started feeling sick. She was COVID positive on admission and started on Paxlovid. Shortness of breath improved with IV lasix. She was transitioned back to her home Lasix 40 mg qD. She was somewhat hypotensive during her admission and her carvedilol, lisinopril, spironolactone, IMDUR, prn Nitrostat were held. These will be discontinued at discharge and she will need to follow up with her PCP in 2-3 days to discuss resuming these.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- 8/12 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC-- detected
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 18.06.2021
- Beginn
- 17.07.2022
- Tage bis Beginn
- 394,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaemia
COVID-19
Delivery
Dyspnoea
Maternal exposure before pregnancy
SARS-CoV-2 test positive
Uterine contractions during pregnancy
Symptomtext
7/17--7/20 30y.o. G4P2012 at 28w3d by L=1st trimester who c/o SOB that has been getting progressively worse over the past two weeks. The pt came to triage mostly because she was worried about how the baby is being affected by her anemia and symptoms. Began having contractions 7/18. 7/19 SVD of baby. Pt and baby discharged 7/20.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 3,0
- Labordaten
- 7/18 -- SARS-CoV-2 by NAA, detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 20.07.2021
- Beginn
- 30.07.2022
- Tage bis Beginn
- 375,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Chest X-ray abnormal
Cough
Dyspnoea
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Symptoms of weakness, cough, nasal congestion, sore throat, mild SOB, and tested positive for Covid on 7/30/22, CXR showed possible COVID pneumonia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- SARS-COV-2 (COVID-19) by NAA, Micro.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- chronic back pain
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 29.07.2022
- Impfdatum
- 09.07.2021
- Beginn
- 13.07.2022
- Tage bis Beginn
- 369,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Bladder catheterisation
COVID-19
Condition aggravated
Confusional state
Dementia
Hydronephrosis
Parkinson's disease
SARS-CoV-2 test positive
Toxic encephalopathy
Urinary retention
Symptomtext
Patient with 3 COVID Moderna vaccinations admitted COVID detected test. Provider d/c note below: "78 YO male history of chronic obstructive pulmonary disease, hypertension, sleep apnea, Parkinson's disease, recent COVID infection presented with weakness and confusion. Patient subsequently admitted for evaluation and management of acute toxic, metabolic encephalopathy. During his hospitalization stay, who suspected that his encephalopathy is stemming from recent COVID infection, worsening dementia in association with his Parkinson's disease and also medication induced from recent ropinirole increased. Psychiatry was consulted who started patient on Zyprexa and decrease his dose of ropinirole. He was also reported to have urinary retention with bilateral moderate hydronephrosis that resolved post Foley placement. His encephalopathy has resolved after Zyprexa, decreased ropinirole dose and resolution of his urinary retention. He will be transferred to Rehab. "
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 16,0
- Labordaten
- COVID detected test 07/06/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pure hyperglyceridemia 1/11/2017 Parkinson disease 4/16/2015 Hyperlipidemia 4/16/2015 Essential hypertension 4/16/2015 Neuropathy with IgG monoclonal gammopathy 3/17/2022 Stage 2 moderate COPD by GOLD classification 3/24/2022 Neuromuscular respiratory weakness 3/24/2022 Renal cyst, right (Chronic) 7/28/2022 Bradycardia
- Andere Medikamente
- -
- Allergien
- Penicillins
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 22.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Injection site erythema
Injection site swelling
Injection site warmth
Mobility decreased
Pain in extremity
Peripheral swelling
Symptomtext
I had some swelling mainly in the arm. The injection site was really swollen, red, and hot to the touch. My arm was very very sore that I could barely lift it. I had fatigue really bad, and I couldn't keep my eyes open for a few days. I did a telehealth visit and was told to take OTC Tylenol, Advil, and Naproxen. The majority of my symptoms lasted for about 4 or 5 days. Some of the symptoms eased up at that time and lasted a little longer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Type 2 Diabetic, High Blood Pressure, High Cholesterol, IBS, Obstructive Sleep Apnea
- Andere Medikamente
- Viberzi 100mg, Trulicity 0.5mL, 1.5mg, Hydrochlorothiazide 25mg, Buspirone 10mg, Atorvastatin 40mg, Metoprolol 50mg, Omeprazole 20mg, Claritin 10mg, Vitamin D 1,000 IU, Tylenol (possibly), Advil (possibly)
- Allergien
- Acrylic, Latex, Bee stings, Clindamycin, Flu shot, Seasonal allergies
- Vorherige Impfungen
- Flu Vaccine (10/1/2019)- I had redness and swelling at the injection site. I believe it was hot to the touch as well. I had fati
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 26.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Arrhythmia
Cardiac monitoring abnormal
Chest X-ray abnormal
Costochondritis
Electrocardiogram abnormal
Sinus tachycardia
Symptomtext
Costochondritis, angina, arrythmia, and tachycardia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- Emergency Room X-Ray found Costochondritis and angina 07/02/2021. Emergency Room EKG found sinus tachycardia 07/02/2021. Cardiologist 11/19/2021 Heart monitor found tachycardia and arrythmia.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Chapped lips
Feeling hot
Insomnia
Lip haemorrhage
Lip swelling
Mouth swelling
Oral mucosal blistering
Oral pain
Paraesthesia
Pharyngeal swelling
Pruritus
Skin burning sensation
Urticaria
Symptomtext
A few days after my covid vaccine while I was watching tv I felt my face was tingling , I went to the bathroom to look in the mirror and I can see my lip swelling and cracking and it started bleeding. Blisters inside my mouth, from one side of my mouth to the other side of my mouth and pink. My mouth and throat felt swollen. My chin was blistered and my neck. At the top of my chest I broke out with large whelps and they burn and itch. I haven't slept in 2 days. It really bothers me. My mouth hurts. My head felt hot but didn't take my temp. All lasting a week. Treatment: None still have stuff on the top of my chest, like whelps and my mouth, bottom lip still broken and cracked.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- NO
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- Breast caner, lung cancer, licky mitral valve
- Andere Medikamente
- Levothyroxine, Atenolol
- Allergien
- Oysters, Nyquil
- Vorherige Impfungen
- Side effects to all 4 COVID/booster vaccines
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 24.03.2022
- Impfdatum
- 24.07.2021
- Beginn
- 09.01.2022
- Tage bis Beginn
- 169,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Dyspnoea exertional
Fatigue
SARS-CoV-2 test positive
Symptomtext
01/09/22 presents to EC ED for "SOB on exertion with cough and fatigue" "positive for COVID on 1/4 at an Urgent care". PMHx of "CAD, HTN, MI cc"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 29.07.2021
- Beginn
- 30.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Feeling abnormal
Myalgia
Pyrexia
Tremor
Symptomtext
Right hand has shaky tremor; Feels like he got hit by a semi; 104 Fever; Aching everywhere; This spontaneous case was reported by a consumer and describes the occurrence of TREMOR (Right hand has shaky tremor), FEELING ABNORMAL (Feels like he got hit by a semi), PYREXIA (104 Fever) and MYALGIA (Aching everywhere) in a 52-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Jul-2021, the patient experienced TREMOR (Right hand has shaky tremor), FEELING ABNORMAL (Feels like he got hit by a semi), PYREXIA (104 Fever) and MYALGIA (Aching everywhere). At the time of the report, TREMOR (Right hand has shaky tremor), FEELING ABNORMAL (Feels like he got hit by a semi), PYREXIA (104 Fever) and MYALGIA (Aching everywhere) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 30-Jul-2021, Body temperature: 104 (High) 104. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product use was not provided by the reporter. Reportedly, when asked for the expiration date, the only date she had on the card was 28th July, however it was unclear if that was the expiration date or the incorrectly entered date of his 1st dose. She is going to verify with the pharmacy. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210730; Test Name: body temperature; Result Unstructured Data: 104
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 13.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal rigidity
Arthralgia
Back pain
Decreased appetite
Dizziness
Dyspepsia
Intentional dose omission
Joint swelling
Tremor
Symptomtext
She was not getting the second dose; dizzy; sharp stabbing pain on the left side of her back; lack of appetite; ankles were a little swollen; heart burn; right side/middle of her stomach felt a little hard; right knee pain; convulsive shaking in her legs/convulsive shaking in her arms; This spontaneous case was reported by a consumer and describes the occurrence of TREMOR (convulsive shaking in her legs/convulsive shaking in her arms), DIZZINESS (dizzy), BACK PAIN (sharp stabbing pain on the left side of her back), DECREASED APPETITE (lack of appetite) and JOINT SWELLING (ankles were a little swollen) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included High cholesterol (controlled by diet). On 13-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Jul-2021, the patient experienced DIZZINESS (dizzy), BACK PAIN (sharp stabbing pain on the left side of her back), DECREASED APPETITE (lack of appetite) and JOINT SWELLING (ankles were a little swollen). In July 2021, the patient experienced TREMOR (convulsive shaking in her legs/convulsive shaking in her arms), DYSPEPSIA (heart burn), ABDOMINAL RIGIDITY (right side/middle of her stomach felt a little hard) and ARTHRALGIA (right knee pain). On an unknown date, the patient experienced INTENTIONAL DOSE OMISSION (She was not getting the second dose). In July 2021, DYSPEPSIA (heart burn) had resolved. On 16-Jul-2021, BACK PAIN (sharp stabbing pain on the left side of her back) had resolved. At the time of the report, TREMOR (convulsive shaking in her legs/convulsive shaking in her arms), DIZZINESS (dizzy) and JOINT SWELLING (ankles were a little swollen) was resolving and DECREASED APPETITE (lack of appetite), INTENTIONAL DOSE OMISSION (She was not getting the second dose), ABDOMINAL RIGIDITY (right side/middle of her stomach felt a little hard) and ARTHRALGIA (right knee pain) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were reported. No treatment information was provided by the reporter. Company Comment:Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. Further information has been requested. Patient reported that she was going to see her doctor if symptoms do not subside. Most recent FOLLOW-UP information incorporated above includes: On 29-Jul-2021: significant Follow up appended; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. Further information has been requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: High cholesterol (controlled by diet)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 28.06.2021
- Beginn
- 26.07.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Antral follicle count
Blood luteinising hormone decreased
Blood oestrogen decreased
Blood prolactin normal
Blood test
Blood thyroid stimulating hormone decreased
Hot flush
Impaired work ability
Magnetic resonance imaging normal
Malaise
Menopause
Menstrual disorder
Palpitations
Pituitary scan
Somatic symptom disorder of pregnancy
Symptomtext
On 6/28/21 I received my 1st dose, the following cycle was 21 days long (my cycle averages 27 days) with a 10 day luteal phase. On 7/26/21 I received my second dose and was very sick and was off work for several days, visit to the ED for heart palpitations and the following cycle was 22 days long with an 8 day luteal phase. The following cycle was 31 days long with a 9 day luteal phase. The following cycle was a chemical pregnancy and I haven't had a period since. It has been 98 days. I track my hormones with the Mira device and noticed that my estrogen started to wind down cycle after cycle since receiving the vaccine and my LH surge has basically been non-existent. My provider attempted to induce a period but nothing happened so bloodwork was done. In the meantime I have been having some pretty severe hot flashes so the hypothesis was that I was in perimenopause since I am 41. My provider was surprised at the results of the bloodwork. My FSH was 1.67, estrogen <5 and my LH 0.21. My AMH is stable and right for my age, prolactin is normal (11.6) and TSH is normal (1.30) and my follicle count is 6 (normal for my age). So I am not in perimenopause but for some reason my body stopped producing estrogen. I had repeat bloodwork done because my provider couldn?t believe I just stopped producing estrogen and the results were the same. I had an MRI of the pituitary gland done to cover all bases; MRI is normal and no issues with pituitary. I am currently on estrogen patches and prometrium to try to restart estrogen production.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- My FSH was 1.67, estrogen <5 and my LH 0.21. My AMH is stable and right for my age, prolactin is normal (11.6) and TSH is normal (1.30) and my follicle count is 6 (normal for my age).
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Bipolar II stable Resolved pre-diabetes with lifestyle modification
- Andere Medikamente
- -
- Allergien
- Doxycyline
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 03.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure systolic increased
Tachycardia
Symptomtext
I had tachycardia that lasted three days. I than developed elevated systolic blood pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- My primary care put me on losartin to help with the blood pressure
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- back pain eczema
- Andere Medikamente
- zovirax, cyclobenzaprine
- Allergien
- laytex
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 21.06.2021
- Beginn
- 03.02.2022
- Tage bis Beginn
- 227,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Alcohol use
COVID-19
COVID-19 pneumonia
Confusional state
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Slow response to stimuli
Urinary tract infection
Symptomtext
Pt presented to the hospital due to confusion and decreased responsiveness. Pt admitted to alcohol use, she is wheelchair bound from cervical spine injury. Found to have COVID pneumonia and UTI Previously vaccinated with Moderna 5/21/21 & 6/21/21. Discharged 2/8/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 5,0
- Labordaten
- COVID + PCR 2/3/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypotension, peripheral neuropathy, hypothyroidism, chronic idiopathic constipation, cervical spine injury
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 18.06.2021
- Beginn
- 04.02.2022
- Tage bis Beginn
- 231,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest X-ray normal
Chest pain
Constipation
Cough
Enteritis
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Patient presented 2/4/22 for chest pain x3days, constipation x5 days. He also reports fevers over the past 2-3 days, he has had COVID-19 infection 2-3 weeks ago and he has received an outpatient monoclonal antibody last week, his fevers have resolved initially but recurred over the past 2-3 days. He denies any shortness of breath, no pleuritic chest pain, no hemoptysis, reports mild nonproductive cough, denies any headache, blurry vision, lightheadedness or neurology symptoms. COVID-19 infection: Associated with low-grade fever, no infiltrates noted on chest x-ray, personally reviewed chest x-ray. Patient is currently hemodynamically stable, on room air with bedside pulse OX 94%, currently no hypoxia. Status post monoclonal antibody treatment in the outpatient setting about a week ago. Currently no clear indication for Remdesivir or Baricitinib, No indication for dexamethasone, he is chronically on prednisone 10 mg every other day and will continue with this regimen for now. Inhaler and nebulizer treatment P.R.N., supportive treatment with vitamin-C, Pepcid. Patient with history of kidney transplant. Patient likely has enteritis secondary to COVID-19 infection per GI. Discharged from the hospital 2/8/22. Previously vaccinated with Moderna 5/21/21 & 6/18/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 4,0
- Labordaten
- COVID 19 PCR + 2/4/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- History of kidney transplant, on immunosuppressants, on chronic systemic steroids, history of Roux-en-Y, BPH, chronic renal insufficiency, aortic stenosis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 26.07.2021
- Beginn
- 30.01.2022
- Tage bis Beginn
- 188,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Brain natriuretic peptide increased
Cardiac failure congestive
Chest X-ray abnormal
Condition aggravated
Cough
Dyspnoea
Fatigue
Hypervolaemia
Palpitations
Peripheral swelling
Wheezing
Symptomtext
Worsening SOB, cough and wheezing with history of COPD. Pt having fatigue, palpitations and leg swelling. Chest Xray suggestive of mild fluid overload/CHF, BNP 894.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CHF, HTN, COPD, Lung mass, Asthma, Tobacco abuse
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 06.07.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 188,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest X-ray abnormal
Depressed level of consciousness
Dyspnoea
Hypoxia
Mental impairment
Pneumonia
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Patient presented to the ER with SOB. She was febrile at 102 degrees and hypoxic with saturating 87% on 4 L. Chest x-ray showed pneumonia. Patient started on dexamethasone and cefepime IV. Patient received bronchodilators mucolytics. She was on 6 L of oxygen tapered down to 4 L in 24 hours. Patient was more alert and mental status improved. She also received IV fluids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 4,0
- Labordaten
- COVID-19 positive test 1/10/2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 10/21/2021: CAD (coronary artery disease). 2021: CVA (cerebral vascular accident), anemia, anxiety, depression, arthritis, bipolar disorder, CKD (chronic kidney disease), congestive heart failure, COPD (chronic obstructive pulmonary disease), dementia, DM (diabetes mellitus), dyslipidemia, edema of both lower extremities, GERD (gastroesophageal reflux disease), hepatitis A, HTN (hypertension), hypothyroid and insomnia. 12/30/2021: osteoarthritis of right knee, unspecified osteoarthritis type, oxygen dependent, PAD (peripheral artery disease), peripheral vascular disease and sleep apnea.
- Andere Medikamente
- Tylenol Extra Strength (acetaminophen) 500mg tablet, Ventolin HFA 108 (90 base) mcg/ACT HFA (albuterol) inhaler, Norvasc (amlodipine) 10mg tablet, Vitamin C (ascorbic acid) 1000mg (ascorbic acid) tablet, Halfprin (aspirin) 81mg tablet, Symb
- Allergien
- Aldactone, Diazoxide, Hydrochlorothiazide W-triamterene, Isosorbide, Morphine
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 02.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Dry mouth
Dry throat
Dyspnoea
SARS-CoV-2 test negative
Urine analysis
Symptomtext
Several days following administration, pt. developed unusual symptoms that she's never had before that primarily included difficulty breathing from constriction of her airways. OTC antihistamines helped somewhat but because symptoms persisted we went to the emergency room at a local Hospital. She had a battery of tests including a COVID test (which was negative) and a variety of other tests including full blood and urine panel, which did not show any particular cause. Pt was administered steroids and IV benadryl to help her breathe, which seemed to help her, and was discharged after spending about 4-6 hours in the ER. At the ER's recommendation, Pt was examined by a pulmonologist, who concluded her lungs were healthy and had no issue. He suggested that she may be having an unusual allergic reaction to the vaccine and that she should see an allergist. Consultations with an allergist did not produce any suggestions--in our experience typical allergists are not equipped to deal with this kind of reaction. The reaction has persisted for an extremely long period (it is still being felt now, 7 months after the vaccine), and the only thing we've found that helps manage it is taking large doses of OTC antihistamines (e.g., Claritin, Allegra, Zyrtec) on a daily basis. Even then, if pt. engages in any significant physical activity, she gets winded much more easily than in the past. Pt is disabled and largely confined to bed due to her chronic nerve disorder--any significant physical activity increases her pain levels. This sedentary lifestyle combined with the antihistamines is letting her manage the reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- See above. Pt is still looking for any expert who may be familiar with what she could do to deal with her reaction--as noted above, allergists that we have seen have been unable to assist as they have no experience dealing with rare chronic reactions to COVID vaccines. Pt unfortunately has an extensive medical history of issues relating to nerve pain and migraines, but she has never had symptoms of this type before. Also, while this specific reaction only began in the days following her 2nd Moderna dose, she also had a negative reaction to the 1st Moderna dose, albeit much less severe, primarily manifesting as an uncomfortable "dry mouth, dry throat" feeling that lasted several weeks. Pt discussed it with her doctor and they decided to still get the 2nd dose in the hopes that the reaction would be lighter.
- Aktuelle Erkrankungen
- No illnesses other than chronic conditions described below.
- Vorgeschichte
- Chronic nerve disorder (RSDS) and history of migraines; however symptoms relating to these conditions have never resembled the types of reactions to the vaccine.
- Andere Medikamente
- Various medications to treat nerve pain relating to chronic nerve disorder (RSDS) and migraines, primarily morphine sulfate and metaxolone. Also OTC Zegerid.
- Allergien
- Latex, aspirin (causes gastric distress).
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 01.07.2021
- Beginn
- 25.01.2022
- Tage bis Beginn
- 208,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Aspartate aminotransferase increased
COVID-19
Chest X-ray abnormal
Cough
Diarrhoea
Dyspnoea
Dyspnoea exertional
Fatigue
Hypoxia
International normalised ratio increased
Lung infiltration
Malaise
Myalgia
Pain
Pyrexia
Renal function test normal
SARS-CoV-2 test positive
Symptomtext
68-year-old woman with past medical history of high blood pressure and diabetes presents emergency department for evaluation of body aches, generalized malaise, fatigue, diarrhea in the setting of Covid confirmed illness for the past 7 days. She has one sick contact at home, her son but he has not taken a Covid test. She has had 2 vaccines and was due to get her third booster this month. She gets a little short of breath on exertion. She has no chest pain at this time. No leg swelling. This patient is a pleasant 68-year-old female with past medical history of coronary artery disease status post a stent was placed about 3 years ago, history of atrial fibrillation on Coumadin, history of diabetes and hyperlipidemia, who resides with family.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 1,0
- Labordaten
- Patient presented to the ER for evaluation of worsening shortness of breath. Her symptoms started about 1 week ago specifically on 1/18/2022 including dry cough, shortness of breath, generalized muscle aches, fevers, and started to have diarrhea today. Patient is vaccinated for COVID-19. She denies recent travel. Patient is fully anticoagulated with Coumadin. ER course: Patient was awake, alert, oriented, no acute distress. She was hypoxic in the ER to 88% on room air required 2 L/min nasal cannula oxygen to maintain her saturation above 90%. Chest x-ray with mild infiltrate, no evidence of edema or effusion or cardiomegaly. She tested positive for COVID-19. Other labs showed no leukocytosis, mild elevation of AST at 47, normal kidney function, and has elevated INR at 3.3. Patient was admitted for COVID-19 infection and hypoxia.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- DM HTN CAD Afib
- Andere Medikamente
- Current Home Medications 1. aspirin 81 mg oral tablet, chewable : 1 tab(s) orally once a day 2. atenolol 25 mg oral tablet : 1 tab(s) orally 2 times a day 3. atorvastatin 40 mg oral tablet : 1 tab(s) orally once a day (at bedtime) 4. Coumad
- Allergien
- Allergy: - Allegra Allergy; (Drug) Hives - Plavix; (Drug) Hives Intolerance: - aspirin; (Drug) Other See Desc; Itching - Contrast Dye; (Drug Category) Nausea/Vomiting
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 21.07.2021
- Beginn
- 19.01.2022
- Tage bis Beginn
- 182,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Lethargy
Mental status changes
Musculoskeletal stiffness
Pneumonia
Snoring
Symptomtext
CHIEF COMPLAINT: pt. sent in for AMS. recently diagnosed with covid. and PNA. hx. of CVA, DM, non-verbal, arrives with snoring respirations with PEG tube in place. all four extremiteis stiff, pt. responds to painful stimuli which is in WNL, pt. lethargic per caregiver. PROBLEM LIST/PAST MEDICAL HISTORY: Ongoing Anemia Diabetes mellitus Diabetes mellitus type 2 in obese Gastrostomy tube dysfunction H/O: stroke Hyperlipidemia Hypertension Left-sided weakness Paralysis Pressure sore of hip Right hemiplegia S/P percutaneous endoscopic gastrostomy (PEG) tube placement Stool incontinence Urine incontinence Historical No qualifying data
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Diabetes, Hypertension, Hyperlipidemia
- Andere Medikamente
- Unknown
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 01.07.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Anxiety
Arthritis
Condition aggravated
Depression
Diarrhoea
Dyspnoea
Fatigue
Influenza like illness
Laboratory test
Nausea
Pain
Pyrexia
Symptomtext
I experienced a fever that was 102 F, then I was having nausea, SOB but when I got to the hospital they told it was good. I had real bad stomach upset, feeling nauseated. I had diarrhea for one day. I went to the Medical Center Hospital and it just seemed it lingered feeling of fatigue and feeling doomed. I was so depressed, I felt took a lot of me. They did lab work and took my vitals and did not stay at the hospital. They told me it was the effects from the vaccine. I did have a low grade fever and drink plenty of fluids. It felt like I had the flu, body was aching. I also have Rheumatoid Arthritis and since the vaccine my arthritis flared up . My doctor told me that because of the vaccine my Arthritis had flare up. I am hesitant about getting the booster, but I do know I need it. I do not feel like myself before the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Lab work were performed
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Sleep Apnea, Asthma, High Blood Pressure, High Cholesterol
- Andere Medikamente
- Took regular medications in the morning when woke up.
- Allergien
- Fentanyl, Metoprolol, sensitivity to garlic
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 14.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site rash
Pain
Pain in extremity
Paraesthesia
Symptomtext
I took the first dose of Moderna vaccine for COVID-19 at the Pharmacy. I did not have any of the usual symptoms associated with taking the vaccine, such as fever, body discomforts, etc. I have the usual pain associated with the shot at the injection site, according to what the person who gave me the shot said. I was also told that the pain would go away after several days. However, the pain did not gat times it was so severe that it felt as if the needle was still in my arm. The pain is only at the injection site and hurts all of the time. If I hold a book, carry grocery bag of even hold on to the handles of the elliptical machine or trend mill for more than 5 minutes or more my hurts with stinging sharp pain, but only at the site of the injection, I have seen my PCP twice about this, he recommended warm compress to the area, I also it to reported it to the Pharmacy in November if I remember correctly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None. PCP has scheduled me for an x-ray of my arm. I had the shot in my left arm.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Alendronate, Vitamins D, E, calcium, Women 50+ Centrium, and Potassium.
- Allergien
- None that I know of.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 31.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Dysmenorrhoea
Heavy menstrual bleeding
Intermenstrual bleeding
Myalgia
Pyrexia
Symptomtext
Patient bleeding clotting cramping from getting my period the very next day after receiving both shots. The first shot gave me my period and he ate bleeding as well as clotting for more than two weeks with regular bleeding and cramping for another two weeks and total was over 30 days after receiving the first shot. I got the second shot a few weeks ago and had my period the week before getting the shot. This time I had heaven bleeding for two weeks and AM now only. Spotting but still have a lot of cramping. I had a bad fever and muscle aches and pains for a about two days after receiving both of the shots.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Check up with an np at women?s wellness and was discussed and told that it was a rare side effect tans that I wasn?t crazy for thinking so.
- Aktuelle Erkrankungen
- Upper respiratory infection,
- Vorgeschichte
- Irritable bowel syndrome, fibromyalgia,
- Andere Medikamente
- Zyrtec in case of allergic reaction again.
- Allergien
- Na
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 23.10.2021
- Impfdatum
- 30.09.2021
- Beginn
- 07.10.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Gait disturbance
Peripheral swelling
Rash
Rash pruritic
Skin ulcer
Urine analysis
Symptomtext
Sever painful and itchy rash on both arms, similar to hives. Sores/rash on knees, hips, lower back and feet. Rash/sores in feet made it difficult to walk. Swollen hands and feet. Unable to close right hand for several days. Mild shortness of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Urine analysis. I am not aware of the results at this time.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure (controlled with medication)
- Andere Medikamente
- Lisinopril HTC Bupropion Focalin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 19.10.2021
- Impfdatum
- 25.06.2021
- Beginn
- 16.10.2021
- Tage bis Beginn
- 113,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Dyspnoea
Oxygen saturation decreased
Positive airway pressure therapy
SARS-CoV-2 test positive
Vomiting
Symptomtext
Patient presented to hospital with SOB. Patient was vomiting at home and his oxygen dropped to low 50s so she called EMS. Patient was placed on BiPAP and brought to ED for further evaluation. Currently on 3 L, saturating 100%. Afebrile
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- PAtient has a positive PCR COVID test on 10/16/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 18.10.2021
- Impfdatum
- 22.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Back pain
Dyspnoea
Fatigue
Neck pain
SARS-CoV-2 test negative
Swelling
Symptomtext
After first shot, pt experienced sore neck and back, and while these were expected reactions to the shot I told her to contact her clinic if concerned. Later, she called reporting trouble breathing and neck swelling so I told her to get seen. Her symptoms resolved without needing care, she ended up canceling her inhaler. After discussing with her provider, she was given the OK to get second dose from us on 06/22/21. The day after the dose (06/23/21) she said she experienced a full month of feeling fatigued, trouble breathing, and weakness. She ended up doing a telehealth visit with her primary on 07/21/21 and provider said it could have been a covid infection that was present before the vaccine was administered. She was prescribed prednisone and inhaler and symptoms gradually resolved. She got her Flu shot with us on 10/07/21 without issue. Because of scarcity of information it is difficult to determine with certainty but this is more likely a case of covid infection that set in before vaccination, rather than an adverse reaction to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Date unknown, but pt got covid test in late July (over 1 month after the vaccination and onset of symptoms) and it was negative. However, husband became ill before date of pt's second shot and his test came back positive later, after pt was already showing symptoms post-vaccine.
- Aktuelle Erkrankungen
- None, but "My husband had covid right before I got my vaccine, but we didn't find out till after the vaccine, so I might have already gotten covid before my shot"
- Vorgeschichte
- Asthma, Diabetes, hypothyroid, hypertension
- Andere Medikamente
- Levothyroxine, Meclizine, Metformin, Albuterol, Senna, Vitamin D, Amlodipine, Hydrochlorothiazide, Amitriptyline, Atorvastatin
- Allergien
- Gluten, Morphine, Penicillins
- Vorherige Impfungen
- Expected side effects to first Moderna dose on 04/26/21, cleared for second dose by clinic on 06/22/21
- Staat
- NH
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 15.10.2021
- Impfdatum
- 26.06.2021
- Beginn
- 27.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: unbekannt
Asthma
Blood test normal
Bronchitis
Chest X-ray normal
Chest discomfort
Chest pain
Cough
Differential white blood cell count normal
Dyspnoea
Electrocardiogram normal
Fatigue
Feeling hot
Fibrin D dimer normal
Full blood count normal
Hyperhidrosis
Hypersomnia
Impaired work ability
Malaise
Symptomtext
Moderna Vaccine: ? First vaccine- 05/29/2021 ? Second Vaccine- 06/26/2021 05/29/2021- Got my first dose of Moderna COVID vaccine. Felt sick, tired and slept for 2 days but was able to come into work on that Monday (05/31/2021). However still felt drowsy and tired all day. I ended up taking Tuesday off because of still feeling tired and drowsy (which I was told was normal). 06/26/2021- Got my second dose of Moderna COVID vaccine. Within an hour of getting it I felt sick, hot, tired and sweaty and went right to bed. 06/27/2021- Woke up with red blotch on my arm where I got the vaccine. It was extremely painful, hot to touch and my arm had swelled up to the size of a golf ball. I called the pharmacist that had given me the vaccine and he told me it was a ?normal reaction that some people get called COVID arm and should go away in a few days?. 06/28/2021- Woke up wheezing, coughing, chest pressure/pain, sweaty and fatigued. Thought I had just gotten sick with a cold. I took Dayquil and Mucinex to try to relieve the wheezing but it did nothing for my symptoms. Throughout the week my symptoms got worse. 07/09/2021- Wheezing got so bad that it became difficult to breathe. I called my PCP, however I was unable to go into the doctor?s office because of ?COVID symptoms? and with new protocol anyone with COVID symptoms were not allowed in the office. They sent me to Urgent Care. At the visit I had gotten an x-ray to rule out pneumonia. We then discussed that the only thing I have done differently is get the COVID vaccine and she mentioned a possible allergic reaction to something in the vaccine. She then prescribed me with a 5 day course of prednisone steroid and an albuterol inhaler and I was to follow up with my PCP. 07/09/2021 ? 07/19/2021- Wheezing seemed to get better with the prednisone and inhaler. However as soon as I finished the course of steroids all my symptoms had come back and I felt worse. 07/19/2021- I went back to Urgent Care (because again my PCP still wouldn?t allow me to come into the office with these symptoms). I saw a different doctor and he wanted to try to treat me for bronchitis. I was prescribed doxycycline for 10 days and was instructed to keep using my inhaler. 07/23/2021- I called Urgent Care and told them the Doxycycline was making me sick and would make me vomit. It also did nothing for my symptoms. I was instructed to try to finish the 10 day course of Doxycycline and continue using my inhaler. 07/28/2021- Went back to Urgent Care and saw another different doctor. He ordered bloodwork, I had an EKG done and a COVID test (all came back negative or normal). However I was put on another course of steroids and told to continue my inhaler. 08/10/2021- I was finally allowed to come back to my PCP with the negative COVID test results. I was still wheezing with chest discomfort/pressure. I was prescribed a Flovent Inhaler and told to continue the Albuterol inhaler as needed. Follow up scheduled for after vacation. 08/12/2021 ? 08/22/2021- Went on vacation. All symptoms still present. 09/02/2021- Went to PCP for follow up. Still having symptoms and was instructed to continue both inhalers. I was also scheduled for a pulmonary function test at Hospital. 09/21/2021- Went to my appointment at Hospital for the pulmonary function test. 10/01/2021- I got my results from the pulmonary function test. Results were normal. 10/04/2021- Had a follow up with my PCP. Still wheezing and chest discomfort/pressure. I was scheduled for a Methacholine challenge test. Instructed to still use both inhalers. 10/12/2021- Went to Hospital for the Methacholine challenge test. Immediately during the test I had difficulty breathing, sweating, and wheezing got worse. Test was forced to stop after the 4th dose of Methacholine because I went under 70% indicating the likelihood of asthma. Pulmonary appointment is now scheduled for 11/04/2021. 10/12/2021 ? PRESENT- Still feeling chest pressure/tightness and wheezing has increased since taking the Methacholine test. I am continuing both inhalers. 10/15/2021- Got a call from PCP telling me that the results for my Pulmonary function test came back positive. They requested that I come in sooner then pervious scheduled appointment. I was told that I have a extremely high risk of having asthma now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 07/09/2021 - CHEST XRAY RESULTS WERE NORMAL 07/28/2021- COVID TEST/CBC and differential/ D-DIMER/Comprehensive metabolic panel/POCT TROPONIN I (ISTAT) RESULTS WERE NEGATIVE OR NORMAL 09/24/2021-PULMONARY FUNCTION TEST RESULTS CAME BACK NORMAL 10/12/2021- PULMONARY FUNCTION TEST/METHACHOLINE CHALLENAGE RESULTS CAME BACK POSITIVE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Adderall 5mg
- Allergien
- Reglan [Metoclopramide Hcl]-Patient developed transient akathisia with reglan that resolved after about 30 min. No rash or anaphylaxis
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 05.10.2021
- Impfdatum
- 18.06.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 101,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Chest pain
Electrocardiogram
SARS-CoV-2 test
Tachycardia
Symptomtext
Chest Pain. Tachycardia. Pt discharged with pulse ox for home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- COVID test: was done outside the hospital on 9/26. Chest x-ray. EKG
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity, BMI: 36.2. Diverticulosis of large intestine
- Andere Medikamente
- None
- Allergien
- Amoxicillin, Motrin, Tylenol
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 17.07.2021
- Beginn
- 17.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood test
Computerised tomogram
Cough
Dizziness
Dyspnoea
Echocardiogram
Electrocardiogram ambulatory
Palpitations
Paranasal sinus discomfort
Tachycardia
Symptomtext
4 hours after COVID moderna second vaccine, she developed tachycardia, lightheadedness, palpitations, weakness., cough. Progressed to sinus pressure/discomfort, hacking cough, shortness of breath. Symptoms of cough/sinus pressure have improved over time but she still has tachycardia, lightheadedness, palpitations and weakness. We did recommend obtaining a covid diagnostic PCR test at the time but this was not completed by patient, so an actual COVID infection cannot be ruled out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- CTA chest to rule out PE on 8/9/21; bloodwork 8/9/21; 2d ECHO 8/13/21; 24 hr HOLTER 8/17/21. Has been seen in ER (8/9/21) and by cardiology as well.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- chronic cystitis, migraine, low back pain, hypersomnia
- Andere Medikamente
- myrbetriq, miralax, oral contraceptive, Trokendi XR, nurtec, sumatriptan
- Allergien
- seasonal; cats
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 27.09.2021
- Impfdatum
- 27.07.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Chest X-ray
Cough
Dyspnoea
Immediate post-injection reaction
Symptomtext
Asthma exacerbation, cough, shortness of breath. Began right after first dose of Moderna vaccination and still experiencing effects 2 months later. Treatment includes inhalers, corticosteroids, and antibiotics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Chest X-ray - 09/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, Chronic Bronchitis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 17.09.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Cardiac flutter
Chest discomfort
Dizziness
Feeling jittery
Haemorrhage
Injection site pain
Mobility decreased
Myalgia
Nervousness
Paraesthesia
Pruritus
Rash
Urticaria
Vertigo
Symptomtext
post bleeding in the shoulder; Really sore; no energy, felt drained; Feeling jittery; hives; itched; Fluttering/ heart fluttering; nervous; COVID shoulder; slight rash on shoulder, neck, chest and slightly on belly; Dizzy/lightheaded; vertigo; tingling throughout the body like arms; tightness around the chest; couldn't move my shoulder; This spontaneous case was reported by a consumer and describes the occurrence of CARDIAC FLUTTER (Fluttering/ heart fluttering) and HAEMORRHAGE (post bleeding in the shoulder) in a 68-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Drug allergy (Sensitivity to epinephrine.) and Vascular disorder (Patient does have Bleeding disorder). Concomitant products included COLECALCIFEROL (VITAMIN D3), PROBIOTICS NOS, PYRIDOXINE HYDROCHLORIDE (VITAMIN B6), MAGNESIUM and ARGININE for an unknown indication. On 20-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Aug-2021, the patient experienced CARDIAC FLUTTER (Fluttering/ heart fluttering) (seriousness criterion medically significant), DIZZINESS (Dizzy/lightheaded), VERTIGO (vertigo), PARAESTHESIA (tingling throughout the body like arms), CHEST DISCOMFORT (tightness around the chest), MOBILITY DECREASED (couldn't move my shoulder), NERVOUSNESS (nervous), INJECTION SITE PAIN (COVID shoulder) and RASH (slight rash on shoulder, neck, chest and slightly on belly). On 21-Aug-2021, the patient experienced URTICARIA (hives) and PRURITUS (itched). On 22-Aug-2021, the patient experienced ASTHENIA (no energy, felt drained) and FEELING JITTERY (Feeling jittery). On an unknown date, the patient experienced HAEMORRHAGE (post bleeding in the shoulder) (seriousness criterion medically significant) and MYALGIA (Really sore). At the time of the report, CARDIAC FLUTTER (Fluttering/ heart fluttering), HAEMORRHAGE (post bleeding in the shoulder), DIZZINESS (Dizzy/lightheaded), VERTIGO (vertigo), PARAESTHESIA (tingling throughout the body like arms), URTICARIA (hives), PRURITUS (itched), NERVOUSNESS (nervous), INJECTION SITE PAIN (COVID shoulder) and RASH (slight rash on shoulder, neck, chest and slightly on belly) had resolved and CHEST DISCOMFORT (tightness around the chest), MOBILITY DECREASED (couldn't move my shoulder), ASTHENIA (no energy, felt drained), FEELING JITTERY (Feeling jittery) and MYALGIA (Really sore) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment information was provided Company comment Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy (Sensitivity to epinephrine.); Vascular disorder (Patient does have Bleeding disorder)
- Vorgeschichte
- -
- Andere Medikamente
- VITAMIN D3; PROBIOTICS NOS; VITAMIN B6; MAGNESIUM; ARGININE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 16.09.2021
- Impfdatum
- 11.06.2021
- Beginn
- 12.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Condition aggravated
Headache
Laboratory test
Pharyngeal erythema
Throat irritation
Symptomtext
The next day after injection joint pains everywhere followed by a head ache intensifying around 7:30pm. Red irritated throat. Still having these issues. Has seen his PCP several times since the second vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Various Tests Ran
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Norvasc 5mg (once daily) Bayer Aspirin 81mg (once daily) Vitamin D3 (once daily) Zinc 50 mg (once daily) Vitamin C 1000 mg (once daily)
- Allergien
- Hydrocodone Erythromycin
- Vorherige Impfungen
- Yellow Fever Shot: Sweating, bad joint pains, red irritated area on arm.
- Staat
- NH
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 13.09.2021
- Impfdatum
- 23.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Biliary catheter insertion
Blood test
Computerised tomogram
Condition aggravated
Fall
Gait inability
Head injury
Magnetic resonance imaging
Multiple sclerosis
Muscular weakness
X-ray
Symptomtext
An hour later I fell down in house hit my head on coffee table, muscle gave out nad I rode to the Hospital in an ambulance. They admitted me , I could not walk. I had a bad reaction with my MS, and my gallbladder needed to be drain. I was in the hospital for 30 days then they shipped me to rehab for another 30 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 30,0
- Labordaten
- X-rays, MRI, CT scan, blood work
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Multiple Sclerosis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 11.09.2021
- Impfdatum
- 14.07.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 49,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Diarrhoea
Dyspnoea
Fatigue
Headache
Illness
Macular degeneration
Nausea
Rash
Retinal degeneration
Tremor
Vaccination complication
Vaccination site mass
Vomiting
Symptomtext
I have a problem with vision a retinal specialist diagnosed me with macular degeneration and retinal ganglion thinning; I have a problem with vision a retinal specialist diagnosed me with macular degeneration and retinal ganglion thinning; I have a general feeling of illness fatigue my breathing is getting worse and dyspnea/violently sick; Add severe fatigue I did not have any energy and I also had a lump on my injection site; I have a general feeling of illness fatigue my breathing is getting worse and dyspnea; Ongoing episodes of chills and shaking and severe diarrhea; I have a mild rash that comes and goes; I have increased joint pain more than I have had before I have joint instability muscle weakness; After relatively constant headache in the front of my head constant nausea but no vomiting trouble eating; Add severe fatigue I did not have any energy and I also had a lump on my injection site; After relatively constant headache in the front of my head constant nausea but no vomiting trouble eating; vomiting; Ongoing episodes of chills and shaking and severe diarrhea; flets; violently sick; Ongoing episodes of chills and shaking and severe diarrhea/severe diarrhea; This spontaneous case was reported by a consumer and describes the occurrence of MACULAR DEGENERATION (I have a problem with vision a retinal specialist diagnosed me with macular degeneration and retinal ganglion thinning) and RETINAL DEGENERATION (I have a problem with vision a retinal specialist diagnosed me with macular degeneration and retinal ganglion thinning) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was provided by the reporter. Concomitant products included CURCUMIN for Inflammation, ASCORBIC ACID, BETACAROTENE, COPPER, NICOTINAMIDE, SELENIUM, TOCOPHEROL, XANTOFYL, ZINC (LUTEIN +) for Vision abnormal NOS, LEVOTHYROXINE, LIOTHYRONINE, LISINOPRIL, ESTRADIOL, METHYLPHENIDATE, INSULIN ASPART (NOVOLOG), INSULIN GLARGINE (LANTUS), CLONAZEPAM, CAFFEINE, VITAMIN D NOS, CYANOCOBALAMIN (B12-VITAMIN), CALCIUM MEFOLINATE (L METHYLFOLATE), PYRIDOXINE HYDROCHLORIDE (B6), HYDROCODONE and ALBUTEROL SULFATE for an unknown indication. On 14-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 01-Sep-2021, the patient experienced DIARRHEA (Ongoing episodes of chills and shaking and severe diarrhea/severe diarrhea), VACCINATION COMPLICATION (flets), ILLNESS (violently sick), CHILLS (Ongoing episodes of chills and shaking and severe diarrhea) and VOMITING (vomiting). On an unknown date, the patient experienced MACULAR DEGENERATION (I have a problem with vision a retinal specialist diagnosed me with macular degeneration and retinal ganglion thinning) (seriousness criterion medically significant), RETINAL DEGENERATION (I have a problem with vision a retinal specialist diagnosed me with macular degeneration and retinal ganglion thinning) (seriousness criterion medically significant), ILLNESS (I have a general feeling of illness fatigue my breathing is getting worse and dyspnea/violently sick), VACCINATION SITE MASS (Add severe fatigue I did not have any energy and I also had a lump on my injection site), DYSPNOEA (I have a general feeling of illness fatigue my breathing is getting worse and dyspnea), TREMOR (Ongoing episodes of chills and shaking and severe diarrhea), RASH (I have a mild rash that comes and goes), ARTHRALGIA (I have increased joint pain more than I have had before I have joint instability muscle weakness), HEADACHE (After relatively constant headache in the front of my head constant nausea but no vomiting trouble eating), FATIGUE (Add severe fatigue I did not have any energy and I also had a lump on my injection site) and NAUSEA (After relatively constant headache in the front of my head constant nausea but no vomiting trouble eating). At the time of the report, MACULAR DEGENERATION (I have a problem with vision a retinal specialist diagnosed me with macular degeneration and retinal ganglion thinning), RETINAL DEGENERATION (I have a problem with vision a retinal specialist diagnosed me with macular degeneration and retinal ganglion thinning), ILLNESS (I have a general feeling of illness fatigue my breathing is getting worse and dyspnea/violently sick), DIARRHEA (Ongoing episodes of chills and shaking and severe diarrhea/severe diarrhea), VACCINATION SITE MASS (Add severe fatigue I did not have any energy and I also had a lump on my injection site), DYSPNOEA (I have a general feeling of illness fatigue my breathing is getting worse and dyspnea), TREMOR (Ongoing episodes of chills and shaking and severe diarrhea), VACCINATION COMPLICATION (flets), ILLNESS (violently sick), RASH (I have a mild rash that comes and goes), ARTHRALGIA (I have increased joint pain more than I have had before I have joint instability muscle weakness), HEADACHE (After relatively constant headache in the front of my head constant nausea but no vomiting trouble eating), CHILLS (Ongoing episodes of chills and shaking and severe diarrhea), FATIGUE (Add severe fatigue I did not have any energy and I also had a lump on my injection site), NAUSEA (After relatively constant headache in the front of my head constant nausea but no vomiting trouble eating) and VOMITING (vomiting) outcome was unknown. No treatment information was provided by the reporter. Patient had suspended her inflammation medication (curcumin phytosome) so that it would not interfere with the efficacy of the vaccine. Now that she tried to take it again and discovered that she cannot go back to the old medication. Company Comment: Very limited information regarding these events has been provided at this time. Additional information required. Most recent FOLLOW-UP information incorporated above includes: On 02-Sep-2021: Significant follow up received on 02 SEP 2021 included addition of start date of events and concomitant drugs.; Sender's Comments: Very limited information regarding these events has been provided at this time. Additional information required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- LEVOTHYROXINE; LIOTHYRONINE; LISINOPRIL; ESTRADIOL; METHYLPHENIDATE; NOVOLOG; LANTUS; CLONAZEPAM; CAFFEINE; VITAMIN D NOS; B12-VITAMIN; L METHYLFOLATE; B6; HYDROCODONE; ALBUTEROL SULFATE; LUTEIN +; CURCUMIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 09.09.2021
- Impfdatum
- 26.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac stress test
Dizziness
Dyspnoea
Electrocardiogram normal
Pallor
Respiratory tract congestion
Symptomtext
The day after my vaccine I was congested for about two days and then late on the second day I had a couple dizzy spells. On the third day when I woke up, I was having trouble breathing and my heart felt restricted. As the day went on, it got so bad that I felt faint and people said I looked pale. I called the ambulance at my work and they brought me to the ER. On the way there they gave me oxygen and gave me aspirin. The following morning I saw a cardiovascular DR. She said everything looked fine and I followed up with my primary DR. My PCD said it was definitely a reaction to the vaccine that I got and advised me not to get the second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Stress test - normal - July 31, 2021, EKG - normal - July 30, 2021, EKG - normal - July 31, 2021
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- 1xdaily: Vitamin B3, Lisinopril HCTZ 20-25MG, duloxetine hcl 60MG
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 02.09.2021
- Impfdatum
- 06.06.2021
- Beginn
- 06.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Arthralgia
Balance disorder
Bursitis
Decreased appetite
Fatigue
Feeling abnormal
Feeling jittery
Headache
Inappropriate schedule of product administration
Influenza
Insomnia
Malaise
Myalgia
Nausea
Neck pain
Pain
Pain in extremity
Symptomtext
Small bruise at injection site after the 2nd dose; Anxiety; loss of Appetite; balance issues; hands shacky; Brain fog; MRI confirmed Bursitis; soreness continued to worsen expanded to neck; General Feeling of unwellness; soreness continued to worsen expanded to shoulder blade entire shoulder upper arm to elbow; Injection was inserted too high on left arm; body aches, arm soreness(left); fever; headaches, frequent headaches; nausea, frequent nausea; fatigue, Chronic fatigue; left arm soreness, soreness continued to worsen; pain; flu symptoms; Insomnia; jittery, jitteryness; 2nd dose on 20 JUl 2021; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE BRUISING (Small bruise at injection site after the 2nd dose), INFLUENZA (flu symptoms), INSOMNIA (Insomnia), FEELING JITTERY (jittery, jitteryness) and ANXIETY (Anxiety) in a 60-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 040C21A and 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 06-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Jul-2021 at 5:00 PM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 06-Jun-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose on 20 JUl 2021). On 21-Jul-2021, the patient experienced INFLUENZA (flu symptoms), INSOMNIA (Insomnia), FEELING JITTERY (jittery, jitteryness), PAIN (pain), PAIN IN EXTREMITY (left arm soreness, soreness continued to worsen), PYREXIA (fever), HEADACHE (headaches, frequent headaches), NAUSEA (nausea, frequent nausea), FATIGUE (fatigue, Chronic fatigue) and MYALGIA (body aches, arm soreness(left)). On 24-Jul-2021, the patient experienced VACCINATION SITE BRUISING (Small bruise at injection site after the 2nd dose), ANXIETY (Anxiety), DECREASED APPETITE (loss of Appetite), BALANCE DISORDER (balance issues), TREMOR (hands shacky), FEELING ABNORMAL (Brain fog), BURSITIS (MRI confirmed Bursitis), NECK PAIN (soreness continued to worsen expanded to neck), MALAISE (General Feeling of unwellness), ARTHRALGIA (soreness continued to worsen expanded to shoulder blade entire shoulder upper arm to elbow) and WRONG TECHNIQUE IN PRODUCT USAGE PROCESS (Injection was inserted too high on left arm). The patient was treated with ACETAMINOPHEN at an unspecified dose and frequency and IBUPROFEN at an unspecified dose and frequency. On 20-Jul-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose on 20 JUl 2021) had resolved. On 24-Jul-2021, INFLUENZA (flu symptoms), INSOMNIA (Insomnia), FEELING JITTERY (jittery, jitteryness), PYREXIA (fever), HEADACHE (headaches, frequent headaches), NAUSEA (nausea, frequent nausea), FATIGUE (fatigue, Chronic fatigue) and MYALGIA (body aches, arm soreness(left)) had resolved with sequelae. At the time of the report, VACCINATION SITE BRUISING (Small bruise at injection site after the 2nd dose) had resolved, ANXIETY (Anxiety), DECREASED APPETITE (loss of Appetite), BALANCE DISORDER (balance issues), TREMOR (hands shacky), PAIN (pain), FEELING ABNORMAL (Brain fog), BURSITIS (MRI confirmed Bursitis), NECK PAIN (soreness continued to worsen expanded to neck), MALAISE (General Feeling of unwellness), ARTHRALGIA (soreness continued to worsen expanded to shoulder blade entire shoulder upper arm to elbow) and WRONG TECHNIQUE IN PRODUCT USAGE PROCESS (Injection was inserted too high on left arm) had not resolved and PAIN IN EXTREMITY (left arm soreness, soreness continued to worsen) had resolved with sequelae. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant medications were reported. This case was linked to MOD-2021-278663 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 18-Aug-2021: Patient demographics, dose details and new events were added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 30.08.2021
- Impfdatum
- 29.06.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Cough
Secretion discharge
Symptomtext
Pt. states that after receiving the 2nd dose of Moderna 06/29/2021, started experiencing symptoms 07/06/2021 of coughing chest pains, and mucus. Primary tele-visit instructed to control at home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 28.07.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Fatigue
Feeling abnormal
Malaise
Mobility decreased
Pain
Pyrexia
Symptomtext
felt a little weird after the shot and felt like she had covid all over again; could not lift her arm for about 7 days / could not stand on feet for 2-3 days; sore arm / had extreme body aches / still had extreme body aches; high fever of 103 degrees F while she was on Tylenol / still experiencing low grade fever from 99 to 100 degrees F (higher temperature close to 100 towards night time); extreme tiredness / very tired at times and have to lay down; started feeling very sick and lasted for 3 days; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (started feeling very sick and lasted for 3 days), FEELING ABNORMAL (felt a little weird after the shot and felt like she had covid all over again), MOBILITY DECREASED (could not lift her arm for about 7 days / could not stand on feet for 2-3 days), PAIN (sore arm / had extreme body aches / still had extreme body aches) and PYREXIA (high fever of 103 degrees F while she was on Tylenol / still experiencing low grade fever from 99 to 100 degrees F (higher temperature close to 100 towards night time)) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 (Patient was hospitalized but completely recovered.) in March 2021. Concomitant products included AMLODIPINE, ATORVASTATIN, CITALOPRAM HYDROBROMIDE (CITALOPRAM HBR), CIMETIDINE, HYDROCHLOROTHIAZIDE, VALSARTAN (VALSARTAN HCTZ), LEVOTHYROXINE and PARACETAMOL (TYLENOL) for an unknown indication. On 28-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Jul-2021, the patient experienced MALAISE (started feeling very sick and lasted for 3 days). On an unknown date, the patient experienced FEELING ABNORMAL (felt a little weird after the shot and felt like she had covid all over again), MOBILITY DECREASED (could not lift her arm for about 7 days / could not stand on feet for 2-3 days), PAIN (sore arm / had extreme body aches / still had extreme body aches), PYREXIA (high fever of 103 degrees F while she was on Tylenol / still experiencing low grade fever from 99 to 100 degrees F (higher temperature close to 100 towards night time)) and FATIGUE (extreme tiredness / very tired at times and have to lay down). At the time of the report, MALAISE (started feeling very sick and lasted for 3 days) and MOBILITY DECREASED (could not lift her arm for about 7 days / could not stand on feet for 2-3 days) had resolved, FEELING ABNORMAL (felt a little weird after the shot and felt like she had covid all over again) and FATIGUE (extreme tiredness / very tired at times and have to lay down) outcome was unknown and PAIN (sore arm / had extreme body aches / still had extreme body aches) and PYREXIA (high fever of 103 degrees F while she was on Tylenol / still experiencing low grade fever from 99 to 100 degrees F (higher temperature close to 100 towards night time)) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, Body temperature: 103 (High) high. On 10-Aug-2021, Body temperature: 99-100 (Low) low grade fever from 99 to 100 degrees F (higher temperature close to 100 towards night time). The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. She had high fever of 103 degrees Fahrenheit (F) while she was on Tylenol. 13 days later she is still experiencing low grade fever from 99 to 100 degrees F (higher temperature close to 100 towards night time), still has extreme body aches, very tired at times and have to lay down. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: body temperature; Result Unstructured Data: high; Test Date: 20210810; Test Name: body temperature; Result Unstructured Data: low grade fever from 99 to 100 degrees F (higher temperature close to 100 towards night time)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (Patient was hospitalized but completely recovered.)
- Andere Medikamente
- AMLODIPINE; ATORVASTATIN; CITALOPRAM HBR; CIMETIDINE; VALSARTAN HCTZ; LEVOTHYROXINE; TYLENOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 15.05.2021
- Beginn
- 14.06.2021
- Tage bis Beginn
- 30,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest X-ray
Chest pain
Cough
Dizziness
Dyspnoea
Electrocardiogram
Full blood count
Impaired work ability
Myalgia
Neck pain
Odynophagia
Pleurisy
SARS-CoV-2 test
Sensitivity to weather change
Symptomtext
pressure and pain upon swallowing; a slight periodic cough; pain upon inhalation; had missed work; arm pain; Lightheadedness; chest pain(chest was sensitive to the touch); Neck pain; breathing difficulty worsening/pain upon inhalation; having a hard time acclimating to the weather (he noticed slight difficulty with breathing)/difficulty breathing; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 29-Jun-2021 and was forwarded to Moderna on 29-Jun-2021. This spontaneous case was reported by a consumer and describes the occurrence of SENSITIVITY TO WEATHER CHANGE (having a hard time acclimating to the weather (he noticed slight difficulty with breathing)/difficulty breathing), DYSPNOEA (breathing difficulty worsening/pain upon inhalation), DIZZINESS (lightheadedness), CHEST PAIN (chest pain(chest was sensitive to the touch)) and NECK PAIN (neck pain) in a 39-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 023C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 15-May-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Jun-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 14-Jun-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced SENSITIVITY TO WEATHER CHANGE (having a hard time acclimating to the weather (he noticed slight difficulty with breathing)/difficulty breathing). On 20-Jun-2021, the patient experienced DYSPNOEA (breathing difficulty worsening/pain upon inhalation). On 24-Jun-2021, the patient experienced DIZZINESS (lightheadedness), CHEST PAIN (chest pain(chest was sensitive to the touch)), NECK PAIN (neck pain), PLEURISY (pain upon inhalation), IMPAIRED WORK ABILITY (had missed work) and MYALGIA (arm pain). On 27-Jun-2021, the patient experienced COUGH (a slight periodic cough). On 29-Jun-2021, the patient experienced ODYNOPHAGIA (pressure and pain upon swallowing). The patient was treated with IBUPROFEN at a dose of 1 dosage form. On 26-Jun-2021, IMPAIRED WORK ABILITY (had missed work) had resolved. At the time of the report, SENSITIVITY TO WEATHER CHANGE (having a hard time acclimating to the weather (he noticed slight difficulty with breathing)/difficulty breathing), DYSPNOEA (breathing difficulty worsening/pain upon inhalation), DIZZINESS (lightheadedness), CHEST PAIN (chest pain(chest was sensitive to the touch)), NECK PAIN (neck pain), COUGH (a slight periodic cough), ODYNOPHAGIA (pressure and pain upon swallowing), PLEURISY (pain upon inhalation) and MYALGIA (arm pain) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Chest X-ray: normal (normal) chest was sensitive to the touch. On an unknown date, Electrocardiogram: normal (normal) normal. On an unknown date, Full blood count: normal (normal) normal. On an unknown date, SARS-CoV-2 test: negative (Negative) negative. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication details were reported. Action taken with mRNA-1273 in response to the events was not applicable. He has been going for another chest x-ay and to schedule an echocardiogram. Physician prescribed an inflammatory which he had not picked up yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210624; Test Name: Chest x-ray; Result Unstructured Data: chest was sensitive to the touch; Test Date: 20210624; Test Name: Electrocardiogram; Result Unstructured Data: normal; Test Date: 20210624; Test Name: Full blood count; Result Unstructured Data: normal; Test Date: 20210624; Test Name: SARS-CoV-2 test; Test Result: Negative ; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No Medical History was provided by the reporter.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 26.08.2021
- Impfdatum
- 12.06.2021
- Beginn
- 14.06.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Dermatitis
Erythema
Fatigue
Impaired work ability
Muscle twitching
Pruritus
Rash
Skin erosion
Skin exfoliation
Urticaria
Symptomtext
Following my first shot I developed hives and rash. I began taking Benadryl. The rash spread from my arm to my scalp, back of my neck, my ears, down my arm and my chest. My scalp was just beginning to resolve when I got my second shot. Following the second shot the rash spread to my legs, my middle back, my lower back, further on my chest. After 7 weeks on 7/31 I went to Urgent Care because I woke up twitching due to the itch. I was given 5 days worth of Prednisone and generic Atarax to take instead of Benadryl. With the prednisone my hives began to clear up and I was more comfortable. However, once I was finished with the prednisone the hives came back and the rash continued to spread. I decided the Atarax wasn't helping and went back to Benadryl. I missed an entire week of work from 8/16-20 because I was so very tired. By this time I was also starting to shed skin and had raw patches on my thighs and my face which made wearing clothing very painful. During this week I decided to stop the Benadryl and I found I had more stamina. I returned to work on 8/23. I currently still have hives, although not as many, my skin is still very inflamed. My scalp, arms and legs are shedding skin. I believe the rash is beginning to resolve but I am now in the 11th week of this. I am still very itchy and some parts are painful. I don't not know how much longer it will take to resolve. The doctor did tell me my skin redness may take months to resolve but I understood that my hives and itchiness should resolve.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Calcium
- Allergien
- Penicillin, Sulfa drugs and seasonal hay fever
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 23.08.2021
- Impfdatum
- 29.07.2021
- Beginn
- 31.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Chest pain
Symptomtext
Chest pains on left side- Steady for 15 days Shoulder pains on left side - Steady for 15 days Severe Chest Pain in the middle of the night 10 days after the second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Factor 5
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 18.08.2021
- Impfdatum
- 24.05.2021
- Beginn
- 22.06.2021
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hyperhidrosis
Hypoaesthesia
Paraesthesia
Rash
Vaccination site rash
Symptomtext
Have a red spot near the injection site. That looks like a rash; Rash, sweats, numbness and tingling; Rash, sweats, numbness and tingling; Rash, sweats, numbness and tingling; Rash, sweats, numbness and tingling; This spontaneous case was reported by a consumer and describes the occurrence of HYPERHIDROSIS (Rash, sweats, numbness and tingling), HYPOAESTHESIA (Rash, sweats, numbness and tingling), PARAESTHESIA (Rash, sweats, numbness and tingling), RASH (Rash, sweats, numbness and tingling) and VACCINATION SITE RASH (Have a red spot near the injection site. That looks like a rash) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 051C21A) for COVID-19 vaccination. Sojgrens, Lupus, arthritis, small fiber neuropathy. Concurrent medical conditions included Sjogren's, Lupus syndrome, Arthritis and Small fiber neuropathy. On 24-May-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form once. On 21-Jun-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 22-Jun-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced HYPERHIDROSIS (Rash, sweats, numbness and tingling), HYPOAESTHESIA (Rash, sweats, numbness and tingling), PARAESTHESIA (Rash, sweats, numbness and tingling) and RASH (Rash, sweats, numbness and tingling). On an unknown date, the patient experienced VACCINATION SITE RASH (Have a red spot near the injection site. That looks like a rash). At the time of the report, HYPERHIDROSIS (Rash, sweats, numbness and tingling), HYPOAESTHESIA (Rash, sweats, numbness and tingling), PARAESTHESIA (Rash, sweats, numbness and tingling), RASH (Rash, sweats, numbness and tingling) and VACCINATION SITE RASH (Have a red spot near the injection site. That looks like a rash) had not resolved. Concomitant products were not reported. No treatment information was provided by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 25-Jun-2021: Follow up received on 25-Jun-2021 contains significant information and an event is added(Have a red spot near the injection site) with unknown date and unknown outcome.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Arthritis; Lupus syndrome; Sjogren's; Small fiber neuropathy
- Vorgeschichte
- Comments: Sojgrens, Lupus, arthritis, small fiber neuropathy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 17.08.2021
- Impfdatum
- 29.07.2021
- Beginn
- 30.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Condition aggravated
Symptomtext
My asthma has been SIGNIFICANTLY worse since receiving the vaccine, there has been no other changes in anything else in my environment or life that would account for this. I do not believe it?s a coincidence, it has not gotten better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- Albuterol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 14.08.2021
- Impfdatum
- 07.07.2021
- Beginn
- 07.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blindness
Dizziness
Dyspnoea
Hyperhidrosis
Pallor
Tremor
Symptomtext
After 10 minutes of the patient vaccine administration, he referred feeling very dizzy with difficulty to breath . He was pale, sweaty, trembling . He referred loss of vision. The patient was seated and his blood pressure was measured with results: (1) 83/45mmHg (2) 102/67mmHg (3) 115/70mmHg 911 was called since the patient was debilitated. He left with the ambulance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- retrieved from his medication history: ICD 10 codes- Z83.3, z03.89, F12.20, F41.0, 536.3, V71.09
- Andere Medikamente
- Bupropion XL 150mg Clonazepam 1mg
- Allergien
- shellfish
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 02.08.2021
- Impfdatum
- 23.04.2021
- Beginn
- 24.04.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Breast mass
Injection site mass
Injection site pain
Injection site pruritus
Injection site rash
Injection site swelling
Mass
Paraesthesia
Peripheral swelling
Pruritus
Rash
Symptomtext
Vx 1: swelling, itching and rash on right arm - from shoulder to wrist Vx2: swelling, itching, rash, pins and needles, pain, baseball sized lump on inj site, lumps under skin on right arm, right breast, right side of torso.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lithium, Atorvastatin, Metformin, Seroquel, Hydroxizine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 02.08.2021
- Impfdatum
- 31.07.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dyspnoea
Hyperhidrosis
Pain
Pain in extremity
Tremor
Symptomtext
Extreme pain on the left side of the body in chest and legs, shaking, sweating and difficulty breathing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 31.07.2021
- Impfdatum
- 31.07.2021
- Beginn
- 31.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fall
Hyperhidrosis
Ocular hyperaemia
Pallor
Tremor
Symptomtext
PATIENT WAS SWEATING, AND SHIVERING. HE BECAME PALE AND HIS EYE WERE RED. HE DRANK WATER. THEN HE WAS SHAKING AND FALLING. HIS DAUGHTER CALLED 911.AMBULANCE CAME. PARAMEDICS CHECKED HIM. HE WAS FEELING BETTER THAT TIME. THEY DIDN'T TAKE HIM TO HOSPITAL .HE CAME TO PHARMACY AND SAID HE IS NORMAL AND LEFT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 29.07.2021
- Impfdatum
- 02.07.2021
- Beginn
- 04.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Antinuclear antibody positive
Arthralgia
Arthritis
Blood test normal
C-reactive protein increased
Complement factor C3 increased
Inflammation
Mobility decreased
Oedema peripheral
Pain
Pain in extremity
Peripheral swelling
Rheumatoid factor negative
Ultrasound scan normal
White blood cell count increased
X-ray normal
Symptomtext
The effects began with pain and inflammation in my right foot on July 4th. The pain and inflammation later escalated to my right arm, and thus I could not move them much. I visited a clinic on July 6th to no avail, and was referred to the hospital for testing. I visited a Medical Center on July 8th and received blood tests, x-rays, and ultrasounds. The tests all came back clear. I was prescribed naproxen for the inflammation. The next day, July 9th, my left foot was then inflamed and painful. I visited another physician on July 13th for a second opinion, and was prescribed furosemide as they had told me I had edema in my feet. On the evening of July 14th, I had begun to get a sharp pain in my right hip and thigh. The pain soon escalated well into midnight (July 15), and at that point, I could no longer move without a shooting pain that was unbearable. I visited the Hospital the same day, and again received multiple tests, including blood, ultrasound, and x-rays. I was there until the next day, and was given an anti-inflammatory shot, and was told to continue to take the naproxen for the rest of the dosage. As of today, July 29th, my swelling and pain have mostly gone down in my feet and arm, but I continue to have flare-ups of pain in the joints, and I now have pain and inflammation in my right knee. Any sort of joint inflammation was rare for me before I was vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- 2,0
- Labordaten
- Tests received (July 15) C-reactive protein: 1.4 mg/dL Anti-nuclear antibody: Positive ANA pattern: Diffuse and Speckled ANA titer 1: 1:160 Rheumatoid factor: <10.0 IU/mL C3 complement: 192 mg/dL WBC: 12.70x10(9)/L
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin, Amoxicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 28.07.2021
- Impfdatum
- 30.06.2021
- Beginn
- 28.07.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Hypoaesthesia
Inflammation
Mobility decreased
Pain
Pain in extremity
Paraesthesia
Paraesthesia oral
Peripheral swelling
Symptomtext
Within a few minutes of receiving injection, my arm went numb from site of injection to the tips of my fingers. Experienced severe swelling, inflammation and pain in whole arm. Fingertips were numb and tingled with the sensation of pins and needles on them. Arm remained inflammed, swollen and in severe pain for two weeks weeks and then decided to see a doctor. Doctor said it should go away fully in two more weeks and that if it did not to come back and see her. It had been the two weeks since I have seen the doctor and full use of my arm is still not fully restored and still feels pain when I try to resume full normal use of it. Also had some slight dizziness and sensation on tongue after two weeks of shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Bupropion
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 27.07.2021
- Impfdatum
- 24.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dyspnoea
Migraine
Symptomtext
2-3 days after the 2nd shot patient experience Migrains , shortness of breath and chest pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Advil dual action
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 22.07.2021
- Impfdatum
- 30.05.2021
- Beginn
- 04.06.2021
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Condition aggravated
X-ray
Symptomtext
Went to be seen at clinic for pain in collar bone. Xray showed arthritis in shoulder ac joint. And a month later had pain in knee and xray showed arthritis. So thinking arthritis flared up from covid shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- X-rays.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Spiralactone, Doxycycline, Naproxen
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 21.07.2021
- Impfdatum
- 30.06.2021
- Beginn
- 03.07.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Feeling of body temperature change
Headache
Hot flush
Mobility decreased
Pain
Symptomtext
Extreme head and body aches, cold and hot flashes, high temperature, in bed for 5 days straight, couldn't move my neck or upper body without extreme pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Paxil 20mg
- Allergien
- Moraine Sulfa Drugs Latex
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 21.07.2021
- Impfdatum
- 15.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood glucose normal
Blood lactic acid
Blood magnesium normal
Body temperature increased
Chills
Dehydration
Differential white blood cell count
Electrocardiogram T wave abnormal
Full blood count
Influenza virus test negative
Lipase normal
Lymphocyte percentage decreased
Mean cell volume increased
Metabolic function test
Nausea
Neutrophil count increased
Neutrophil percentage increased
Symptomtext
A few hours after receiving 2nd Covid vaccine patient began feeling nauseated then started vomiting. She denies blood in the emesis. She also endorses feeling "chilled to the bone." Triage temp is 103.1. Patient denies chest pain, shortness of breath, cough, numbness, tingling, falls, headache, abdominal pain, diarrhea, constipation, changes in diet, recent travel. No dysuria, hematuria, rashes, bruising or bleeding. She states she has had at least 6 or 7 episodes of emesis and is on her fourth emesis bag in the ER. She states she feels very dehydrated and week. I was informed that the patient was admitted and was under the care of a hospitalist who I could not reach.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- Physical exam 7/15 All 7/15 Lactic Acid 3.1 (HH) Magnesium 1.6 (L) Comprehensive metabolic panel - Glucose 136 (H) other values within range Lipase 56 CBC with Automated DIFF WBC 16.5 (H) RBC 3.89 (L) MCV 101.3 (H) Neutrophils 80 (H) Lymphocytes 15 (L) ABS Neutrophils 13.2 (H) All others within ref range EKG, 12 Lead Initial VR 121 AR 121 PR Interval 162 QRS 74 Q-T Interval 314 QTC Calculated 446 P Axis52 R Axis-27 T Axis66 sinus tachycardia corderline left axis deviation abnormal r wave progrssion borderline t abnormalities Covid, influenza, negative urinalysis normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Mitral Valve prolapse, hypertension, hyperlipidemia, malignancy (mastectomy with reconstructive augmentation), urge incontinence.
- Andere Medikamente
- tamoxifen, oxybutynin chlorideXL, telmisaratan-hydrochlorithiazide, setraline
- Allergien
- Iodine, Penicillin, Latex, Natural Rubber
- Vorherige Impfungen
- Covid-19, unsure of issues
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 18.07.2021
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Peripheral swelling
Pruritus
Rash
Urticaria
Symptomtext
10 day duration: Swollen arm covered with rash, labored breathing, hives, itching all over.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- Levothyrxine, escitalopram, cimetidine, ezetismibe
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 16.07.2021
- Impfdatum
- 16.07.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood pressure increased
Chest pain
Condition aggravated
Heart rate increased
Symptomtext
Complained of chest pain 7/10. Contacted nurse. Nurse questioned and stated that she had not taken b/p meds this morning and was experiencing total body weakness. B/p elevated pulse elevated volunteer MD on site. 911 contacted for further evaluation. Patient taken to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- Trouble breathing
- Vorgeschichte
- Asthma, high b/p
- Andere Medikamente
- Asthma medications, blood pressure medications
- Allergien
- Aspirin
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 15.07.2021
- Impfdatum
- 12.07.2021
- Beginn
- 14.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyskinesia
Jaw disorder
Musculoskeletal discomfort
Paraesthesia
Symptomtext
jaw bone bilateral area of face "jolting sensation" and then right side of lower back tingly, kinda like when foot falls asleep. Have not seen a doctor
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 13.07.2021
- Impfdatum
- 11.07.2021
- Beginn
- 11.07.2021
- 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
Chest pain
Symptomtext
Systemic: Chest Tightness / Heaviness / Pain-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 09.07.2021
- Impfdatum
- 01.06.2021
- Beginn
- 24.06.2021
- Tage bis Beginn
- 23,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac murmur
Chills
Condition aggravated
Fatigue
Headache
Nausea
Symptomtext
Very fatigued...low heart rate (55) in the middle of the day...murmur...chills..headache..nauseous.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Heart murmur/tear in mitral valve..
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 08.07.2021
- Impfdatum
- 24.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Fatigue
Headache
Hyperhidrosis
Injection site induration
Injection site swelling
Injection site warmth
Nausea
Pain
Pyrexia
SARS-CoV-2 test negative
Tremor
Symptomtext
Swelling at injection site and extremely hot to touch and formed a hard mass for over one week and started within an hour of injection. 24 hours later, fatigue, fever, shakes, headache and aches set in. The second night all the previous mentioned symptoms continued but at an elevated state. This integrity lasted for three days. One week post injection, still suffering headaches, nausea, fatigue, shortness of breath, aches and sweats. Two weeks post injection, still suffering from previously mentioned symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 07-01-2021 - Covid test administered - Results of the test were negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Yeast
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 07.07.2021
- Impfdatum
- 23.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Computerised tomogram normal
Tremor
Symptomtext
Day of vaccination, patient experienced uncontrollable tremors in both arms. In response, patient took a dose of ibuprofen, performed stretches and took a nap; symptoms subsided. On June 28th, 2021, patient experienced another bout of tremors in both extremities at around 10am, which persisted for approximately 12 hours. After a televisit with CRNP, patient was referred to Emergency room. Patent reported to Hospital with continuing tremors. Doctors examined the patient's blood, as they head suspected rhabdomyolysis after ruling out any neurological causes for the symptoms. All bloodwork came back negative. Doctors intravenously injected 1.5 liters of saline fluid, after which the tremors subsided. Patient was thus discharged from ER. On July 2, 2021, at around 6pm, patient experienced sporadic tremors in right arm, which subsided after approximately 30 minutes. On July 4th, 2021, patient experienced frequent and sporadic tremors in both arms during the course of the day. Symptoms only subsided with sleep. On July 5th, 2021, patient experienced tremors in all four extremities during the course of the day. Consumed electrolyte water, remembering that the saline IV fluids had previously treated the tremors. Frequency and intensity of tremors decreased after patient consumed 48 fl oz of electrolyte water. Tremors fully subsided in sleep. On July 7th, 2021, patient was admitted to Family Practice and referred for a CT scan while still experiencing tremors. Scan showed no hemorrhages or growths in brain. Patient continues to experience sporadic and frequent tremors in all four extremities, varying in length and intensity.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- 7/2/21: Bloodwork for rhabdomyolysis. Tested negative. 7/6/21: CT scan. No hemorrhages or growths were found.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma Seasonal allergies Overweight
- Andere Medikamente
- Singular, Ventolin HFA, Flovent, Benadryl
- Allergien
- Sensitivity to Augmentin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 06.07.2021
- Impfdatum
- 21.06.2021
- Beginn
- 21.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Chest discomfort
Chest pain
Dyspnoea
Fatigue
Blood potassium decreased
Chest X-ray
Electrocardiogram
Pyrexia
Tearfulness
Troponin
Urine analysis
Symptomtext
?Patient without significant medical history presents with complaint of chest pain short of breath started about 1.5 hours before ED assessment, she awoke from sleep with the symptoms. She did receive her first maternal vaccination yesterday. She did have coronavirus infection this past January 5 months ago. Patient without any cough. She is had fatigue and low-grade fever since she awoke this morning. Had some mild chest discomfort that has improved. She does have shortness of breath. EMS found the patient tachypneic in the 30s and tachycardic to the 130s and anxious and tearful but this has improved on ED arrival. Patient will have supportive care with IV fluids, analgesic effect with IV Tylenol and its antipyretic effect in this patient will be helpful as well. Patient well-appearing, no concern for sepsis. Denies any UTI symptoms. Low suspicion tickborne illness. Disposition based on results of imaging?
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 06.07.2021
- Impfdatum
- 21.06.2021
- Beginn
- 21.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Chest discomfort
Chest pain
Dyspnoea
Fatigue
Blood potassium decreased
Chest X-ray
Electrocardiogram
Pyrexia
Tearfulness
Troponin
Urine analysis
Symptomtext
?Patient without significant medical history presents with complaint of chest pain short of breath started about 1.5 hours before ED assessment, she awoke from sleep with the symptoms. She did receive her first maternal vaccination yesterday. She did have coronavirus infection this past January 5 months ago. Patient without any cough. She is had fatigue and low-grade fever since she awoke this morning. Had some mild chest discomfort that has improved. She does have shortness of breath. EMS found the patient tachypneic in the 30s and tachycardic to the 130s and anxious and tearful but this has improved on ED arrival. Patient will have supportive care with IV fluids, analgesic effect with IV Tylenol and its antipyretic effect in this patient will be helpful as well. Patient well-appearing, no concern for sepsis. Denies any UTI symptoms. Low suspicion tickborne illness. Disposition based on results of imaging?
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.07.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 7+
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Hyperhidrosis
Muscle discomfort
Visual impairment
Symptomtext
He complained breathing problem and sweating and vision problem and twisting muscle few minutes later after first dose Moderna vaccine. He was sitting on chair and I gave him massaging to relax muscle and then called 911. EMT checked his status and then felt better. He denied to go hospital and then he walked out
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- nothing
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 26.06.2021
- Impfdatum
- 24.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Swelling face
Symptomtext
a man came to the pharmacy this morning stating his wife has been experiencing a tingly arm and puffy face after receiving the Moderna covid vaccination. He said she had taken benadryl with no resolution of side effects. It was recommended that she contact her Doctor and to go to be seen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none stated
- Vorgeschichte
- none stated
- Andere Medikamente
- none stated
- Allergien
- none stated
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 23.06.2021
- Impfdatum
- 23.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Feeling hot
Hypoaesthesia
Paraesthesia
Symptomtext
Patient received her 2nd dose of moderna. Within the next 2 mins pt started to have bilateral redness/warmth across both arms. pt was offered diphenhydramine injection and she declined. pt was monitored for a total of 30 mins. Over the 30 mins the pt's redness and warmth did dissipate back to normal. Pt also said she was experiencing some tingling/numbness in her right leg - but did explain she was in a car accident previously so it may have been a unrelated. After the 30 mins pt seemed ok and did leave. She did not experience any shortness of breath, swelling of the tongue/mouth, or chest pain. Pt blood pressure was 119/69
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 23.06.2021
- Impfdatum
- 17.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Blister
Chills
Dehydration
Headache
Impetigo
Migraine
Pain
Pruritus
Pyrexia
Symptomtext
Started out with a migraine at 7 am. By 9 am I had chills, body aches, joint aches, headache, fever of 102. By 12 pm my fever was 104.7. It stayed that high for three hours then came back down to 102 with tylenol and ibuprofen and eventually leveled out at 99 until later in the afternoon. I was dehydrated despite large intake of water and gatorade. The day after the vaccine (6/18/2021) i woke up with blisters around my nostrils. These blisters were itchy, painful, and weeping significantly. Doctor diagnosed the blisters as impetigo and had to be put on antibiotics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Multivitamin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 18.06.2021
- Impfdatum
- 14.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arrhythmia
Chills
Dyspnoea
Lymphadenopathy
Pain in extremity
Pyrexia
Symptomtext
Patient complains of shortness of breath, very sore arm, inflamed lymph node under left arm, chills, fever and heart arrhythmias, Patients states he was in perfect health before receiving the Moderna Vaccine. He refuses to go to a doctor for evaluation. The request that I complete VAERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 17.06.2021
- Impfdatum
- 15.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest X-ray
Chest pain
Dyspnoea
Influenza like illness
Symptomtext
flu like symptoms, shortness of breath, severe chest pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- chest xrays, blood work
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- birth control
- Allergien
- lactose intolerant
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 16.06.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dyspnoea
Hypersensitivity
Pharyngeal swelling
Pruritus
Rash
Urticaria
Symptomtext
Patient reported difficulty breathing, throat swelling, rash/hives/welt, itching. Patient was seen in ER and given several prescriptions to treat allergic reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 19.03.2023
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Laboratory test abnormal
Malaise
Nasopharyngitis
Pyrexia
Symptomtext
Patient states she has been ill ever since she received her second dose of moderna shot. Cold symptoms, fever, chills, no energy to get out of bed. lab work values altered. she states she has seen mutiple specialists since (cardiologist, rheumatologist, gastroenterologist) with no relief.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 10.02.2023
- Impfdatum
- 06.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Malaise
Symptomtext
Hasn't been well since the second dose; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (Hasn't been well since the second dose) in an adult male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 053E21A and 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 06-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In 2022, the patient experienced MALAISE (Hasn't been well since the second dose). At the time of the report, MALAISE (Hasn't been well since the second dose) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product reported by reporter. No treatment medication reported by reporter. This case was linked to MOD-2023-707334 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 01.06.2021
- Beginn
- 01.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Headache
Hypersomnia
Hypoaesthesia
Immediate post-injection reaction
Pyrexia
Sensory loss
Symptomtext
Slept 24 hours after shot, headache, fever for 5 days. Huge wave ran across body directly after administration. Numbness in fingers ever since. Loss of touch/feel in finger tips ever since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Gluten
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 24.09.2022
- Impfdatum
- 23.06.2021
- Beginn
- 24.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Magnetic resonance imaging
Vaccination site pain
X-ray limb
Symptomtext
Vaccination site pain; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (Vaccination site pain) in a 50-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. Co-suspect product included non-company product ADALIMUMAB (HUMIRA) for Crohn's disease. The patient's past medical history included Tobacco user (Four Cigarette Sticks A Day) from 1986 to 2014 and Alcohol use (Beer, Hard Liquor, Variety, Occasionally) from 1990 to 1999. Concurrent medical conditions included Bowel adhesions (Lot Of Scar Tissue In Colon), Bowel obstruction (bowel blockages), Bowel discomfort (Trouble With Bowel Movements), Acid reflux (esophageal) and Crohn's disease. Concomitant products included OMEPRAZOLE (PRILOSEC [OMEPRAZOLE]) for Acid reflux (esophageal). In 2020, the patient started ADALIMUMAB (HUMIRA) (Subcutaneous) 40 milligram once a week. On 23-Jun-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 24-Jun-2021, the patient experienced VACCINATION SITE PAIN (Vaccination site pain). On 26-Jun-2021, VACCINATION SITE PAIN (Vaccination site pain) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2020, Magnetic resonance imaging: Showed torn left rotator cuff and left tendon bicep. In 2020, X-ray limb: Showed torn left rotator cuff and left tendon bicep. The patient had no known allergies. The reporter's causality for the event vaccination site pain was reported as not related to Humira. Primary reporter does not had the lot number information, because the information was not available in the patient's file for Humira. The patient experienced recurrent sore right shoulder due to Covid vaccine. A day after the patient got vaccinated for Covid-19 on each dose patient experienced a sore right shoulder that lasted for two to three days but that was the only side effect No treatment medication were provided. This case was identified as part of a retrospective clean-up activity where certain emails received in the moderna mailbox were missed to be booked-in. This case was linked to MOD-2021-624662 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 2020; Test Name: MAGNETIC RESONANCE IMAGING; Result Unstructured Data: Showed torn left rotator cuff and left tendon bicep; Test Date: 2020; Test Name: SHOULDER X-RAY; Result Unstructured Data: Showed torn left rotator cuff and left tendon bicep
- Aktuelle Erkrankungen
- Acid reflux (esophageal); Bowel adhesions (Lot Of Scar Tissue In Colon); Bowel discomfort (Trouble With Bowel Movements); Bowel obstruction (bowel blockages); Crohn's disease
- Vorgeschichte
- Medical History/Concurrent Conditions: Alcohol use (Beer, Hard Liquor, Variety, Occasionally); Tobacco user (Four Cigarette Sticks A Day)
- Andere Medikamente
- PRILOSEC [OMEPRAZOLE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 05.08.2021
- Beginn
- 02.09.2022
- Tage bis Beginn
- 393,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chills
Pyrexia
Symptomtext
chills, fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 18.06.2021
- Beginn
- 17.07.2022
- Tage bis Beginn
- 394,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Hyporesponsive to stimuli
Mental status changes
Pyrexia
SARS-CoV-2 test positive
Somnolence
Symptomtext
7/19--presently admitted 65y.o. female with past medical history oligodendroglioma s/p chemoradiation with residual right hemiparesis, dementia, cognitive impairment, nonverbal at baseline, hypertension, hypothyroidism, depression, anxiety presenting for altered mental status and fever. Patient is nonverbal at baseline, history obtained from available notes as well as her son at bedside. Discussed her care at length with him. She has been in skilled care facility since May. Family and staff found her difficult to awaken on 7/18. She was minimally responsive. Found to be febrile at that time. No other observed symptoms. At presentation, she tested positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- 7/19 -- SARS-CoV-2 by NAA, detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 04.08.2022
- Impfdatum
- 25.06.2021
- Beginn
- 02.08.2022
- Tage bis Beginn
- 403,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Appetite disorder
Arthralgia
Chills
Decreased activity
Oropharyngeal pain
Pyrexia
Symptomtext
activity change, appetite change, chills, fever, sore throat, arthralgias
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 15.07.2021
- Beginn
- 27.06.2022
- Tage bis Beginn
- 347,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test
Erythema
Gait disturbance
Joint swelling
Pain
Pain in extremity
Peripheral swelling
Pruritus
Skin sensitisation
Urticaria
Symptomtext
swelling in her joints including her knees; has been in tears from the pain; has touch flares on her skin; the skin was super red; had swelling in her hands and feet; couldn't walk at one point and needed to be pushed in a wheelchair; pain in her hands and feet; welt marks all over her stomach; had an itchy response; This spontaneous case was reported by a nurse and describes the occurrence of PRURITUS (had an itchy response), JOINT SWELLING (swelling in her joints including her knees), PAIN (has been in tears from the pain), SKIN SENSITISATION (has touch flares on her skin) and ERYTHEMA (the skin was super red) in a 19-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 056A22A, 049E21A and 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 15-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 16-Jun-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 27-Jun-2022, the patient experienced PRURITUS (had an itchy response) and URTICARIA (welt marks all over her stomach). On an unknown date, the patient experienced JOINT SWELLING (swelling in her joints including her knees), PAIN (has been in tears from the pain), SKIN SENSITISATION (has touch flares on her skin), ERYTHEMA (the skin was super red), PERIPHERAL SWELLING (had swelling in her hands and feet), GAIT DISTURBANCE (couldn't walk at one point and needed to be pushed in a wheelchair) and PAIN IN EXTREMITY (pain in her hands and feet). The patient was treated with TRIAMCINOLONE ACETONIDE (KENALOG [TRIAMCINOLONE ACETONIDE]) at an unspecified dose and frequency and DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at an unspecified dose and frequency. At the time of the report, PRURITUS (had an itchy response), JOINT SWELLING (swelling in her joints including her knees), PAIN (has been in tears from the pain), SKIN SENSITISATION (has touch flares on her skin), ERYTHEMA (the skin was super red), PERIPHERAL SWELLING (had swelling in her hands and feet), PAIN IN EXTREMITY (pain in her hands and feet) and URTICARIA (welt marks all over her stomach) outcome was unknown and GAIT DISTURBANCE (couldn't walk at one point and needed to be pushed in a wheelchair) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2022, Blood test: white count was up. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication details were not reported by the reporter. Patient had some blood work done which showed that white count was up. Patient was also taking oral steroids as treatment drug.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 2022; Test Name: Blood test; Result Unstructured Data: white count was up
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 27.03.2022
- Impfdatum
- 25.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose increased
Blood test
Dizziness
Fatigue
Glycosylated haemoglobin increased
Ketoacidosis
Pollakiuria
Thirst
Type 1 diabetes mellitus
Visual impairment
Symptomtext
The day following the shot, I was very tired and dizzy and thought that was just a side affect. The tiredness/dizziness lasted for a couple weeks where I thought it was still a side affect. By week three, my vision was getting bad and tiredness increased. Also started getting thirsty and urinating more. By August 10th I was admitted into the hospital with Ketoacidosis. Then diagnosed with Type 1 Diabetes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- 3,0
- Labordaten
- Blood work completed first at doctor's office where numbers were in the mid 200s with an A1C of 12 - recommended I go to the hospital that evening then tested with Blood sugar levels at 680 with A1C of 13.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Birth control: Blisovi Fe 1/20
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 24.03.2022
- Impfdatum
- 15.02.2021
- Beginn
- 04.01.2022
- Tage bis Beginn
- 323,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
Blood glucose increased
COVID-19
SARS-CoV-2 test positive
Symptomtext
01/04/22 presents to ED for "worsening abdominal pain and high blood sugar". PMHx of "chronic pancreatitis"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- 01/04/22 SARS-CoV-2 (COVID-19)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 23.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Headache
Malaise
Myalgia
Pyrexia
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (feeling really crappy), COUGH (coughing), HEADACHE (residual head ache), MYALGIA (body aches) and PYREXIA (fever (it got up to 101)) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 006D21A and 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was reported. Concomitant products included FLUOXETINE HYDROCHLORIDE (PROZAC) and DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL ITCH) for an unknown indication. On 23-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 24-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced MALAISE (feeling really crappy), COUGH (coughing), HEADACHE (residual head ache), MYALGIA (body aches), PYREXIA (fever (it got up to 101) and CHILLS (chills). At the time of the report, MALAISE (feeling really crappy), COUGH (coughing), HEADACHE (residual head ache), MYALGIA (body aches), PYREXIA (fever (it got up to 101) and CHILLS (chills) outcome was unknown. No treatment medications were provided by the reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was reported.
- Andere Medikamente
- PROZAC; BENADRYL- ITCH
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 06.06.2021
- Beginn
- 21.06.2021
- Tage bis Beginn
- 15,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Asthenia
Dizziness
Feeling abnormal
General physical health deterioration
Headache
Illness
Myalgia
Pain
Pain in extremity
Pyrexia
Somnolence
Symptomtext
It has gone from bad to worse and she can't work; Dizzy off and on; Weak off and on; She has been sleeping 12-13 hours per night which is not normal for her; He shoulder got worse to the point of throwing up; After her arm stopped hurting her shoulder was in lots and lots of pain / she can't work; Arm hurt; She was sick; Feeling very bad the day after; Fever; Headache; achy all over for 3 days - arm hurt; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Arm hurt), GENERAL PHYSICAL HEALTH DETERIORATION (It has gone from bad to worse and she can't work), PAIN (He shoulder got worse to the point of throwing up), DIZZINESS (Dizzy off and on) and ASTHENIA (Weak off and on) in a 60-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 06-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 21-Jun-2021, the patient experienced PAIN IN EXTREMITY (Arm hurt), ILLNESS (She was sick), FEELING ABNORMAL (Feeling very bad the day after), PYREXIA (Fever), HEADACHE (Headache) and MYALGIA (achy all over for 3 days - arm hurt). On 23-Jun-2021, the patient experienced PAIN (He shoulder got worse to the point of throwing up) and ARTHRALGIA (After her arm stopped hurting her shoulder was in lots and lots of pain / she can't work). On an unknown date, the patient experienced GENERAL PHYSICAL HEALTH DETERIORATION (It has gone from bad to worse and she can't work), DIZZINESS (Dizzy off and on), ASTHENIA (Weak off and on) and SOMNOLENCE (She has been sleeping 12-13 hours per night which is not normal for her). The patient was treated with ACETAMINOPHEN for Adverse event, at a dose of 1 dosage form and IBUPROFEN for Adverse event, at a dose of 1 dosage form. On 23-Jun-2021, PAIN IN EXTREMITY (Arm hurt), ILLNESS (She was sick), FEELING ABNORMAL (Feeling very bad the day after), PYREXIA (Fever), HEADACHE (Headache) and MYALGIA (achy all over for 3 days - arm hurt) had resolved. At the time of the report, GENERAL PHYSICAL HEALTH DETERIORATION (It has gone from bad to worse and she can't work), PAIN (He shoulder got worse to the point of throwing up), DIZZINESS (Dizzy off and on), ASTHENIA (Weak off and on), SOMNOLENCE (She has been sleeping 12-13 hours per night which is not normal for her) and ARTHRALGIA (After her arm stopped hurting her shoulder was in lots and lots of pain / she can't work) outcome was unknown. Concomitant product use was not provided by the reporter. Treatment medication included muscle relaxers and applying dry heat and cold. Patient took second dose on 20-JUL-2021 (040C21A) This case was linked to MOD-2021-278689 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 09.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nasal congestion
Oropharyngeal pain
Symptomtext
Sore throat; Congestion; This spontaneous case was reported by a consumer and describes the occurrence of OROPHARYNGEAL PAIN (Sore throat) and NASAL CONGESTION (Congestion) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced OROPHARYNGEAL PAIN (Sore throat) and NASAL CONGESTION (Congestion). At the time of the report, OROPHARYNGEAL PAIN (Sore throat) and NASAL CONGESTION (Congestion) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications were not provided. Post vaccination patient experienced congestion and sore throat, these symptoms worsen in the morning and lasted for couple of weeks .Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 20.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site pain
Vaccination site pruritus
Vaccination site warmth
Symptomtext
Heat on the injection site; Soreness and heat on the injection site, and it also itches; Soreness and heat on the injection site; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (Heat on the injection site), VACCINATION SITE PRURITUS (Soreness and heat on the injection site, and it also itches) and VACCINATION SITE PAIN (Soreness and heat on the injection site) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The patient's past medical history included Arthritis. Concomitant products included IBUPROFEN for Arthritis, VITAMINS NOS for an unknown indication. On 20-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 27-Jul-2021, the patient experienced VACCINATION SITE WARMTH (Heat on the injection site), VACCINATION SITE PRURITUS (Soreness and heat on the injection site, and it also itches) and VACCINATION SITE PAIN (Soreness and heat on the injection site). At the time of the report, VACCINATION SITE WARMTH (Heat on the injection site), VACCINATION SITE PRURITUS (Soreness and heat on the injection site, and it also itches) and VACCINATION SITE PAIN (Soreness and heat on the injection site) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment includes anti-itching medicine (unspecified) and ice pack.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthritis
- Andere Medikamente
- VITAMINS NOS; IBUPROFEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 22.06.2021
- Beginn
- 31.07.2021
- Tage bis Beginn
- 39,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Inappropriate schedule of product administration
Psychomotor hyperactivity
Symptomtext
hyper - feels like I consumed several cans of Red Bull. Inappropriate schedule of vaccine administered; chills; This spontaneous case was reported by a consumer and describes the occurrence of PSYCHOMOTOR HYPERACTIVITY (hyper - feels like I consumed several cans of Red Bull.), CHILLS (chills) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 040C21A and 051C21A) for COVID-19 vaccination. Concurrent medical conditions included Penicillin allergy, Allergy to antibiotic (Allergy to Erythromycin), House dust mite allergy, Allergic to cats, Allergic to dogs, Allergy to feathers, Cockroach allergy, Grass allergy, Ragweed allergy, Allergy to plants (Allergy to Sorrel, English Plantain, Lamb's Quarters, Pigweed, Cockelbur, Nettle, Palm trees, Melaleuca, Australian Pine, White Pine, Live Oak, Red Cedar Elm, Maple, Ash Cottonwood and Brazilian Pepper tree), Allergy to molds (Allergy to Hormodendrum, Alternaria, Helminhosporium, Fusarium, Pullaria, Aspergillus, Epicoccum, Stemphylium and Curvularia) and Heart murmur (More heart fluttering after first vax, slight heavyness on left side radiating to back.). Concomitant products included BUDESONIDE (RHINOCORT [BUDESONIDE]) for Multiple allergies, DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) from an unknown date to 30-Jul-2021 for Prophylaxis. On 22-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 31-Jul-2021 at 1:43 PM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 31-Jul-2021, the patient experienced PSYCHOMOTOR HYPERACTIVITY (hyper - feels like I consumed several cans of Red Bull.), CHILLS (chills) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). On 31-Jul-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. At the time of the report, PSYCHOMOTOR HYPERACTIVITY (hyper - feels like I consumed several cans of Red Bull.) and CHILLS (chills) outcome was unknown. The patient was not diagnosed with or tested positive for COVID-19. The patient had none acute illness at the time of vaccination and up to one month before. The patient received the second dose the previous day and had not been 24 hours yet. She had been experiencing chills and was hyper felt like she consumed several cans of energy drinks. No treatment medications were reported. This case was linked to MOD-2021-241605 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergic to cats; Allergic to dogs; Allergy to antibiotic (Allergy to Erythromycin); Allergy to feathers; Allergy to molds (Allergy to Hormodendrum, Alternaria, Helminhosporium, Fusarium, Pullaria, Aspergillus, Epicoccum, Stemphylium and Curvularia); Allergy to plants (Allergy to Sorrel, English Plantain, Lamb's Quarters, Pigweed, Cockelbur, Nettle, Palm trees, Melaleuca, Australian Pine, White Pine, Live Oak, Red Cedar Elm, Maple, Ash Cottonwood and Brazilian Pepper tree); Cockroach allergy; Grass allergy; Heart murmur (More heart fluttering after first vax, slight heavyness on left side radiating to back.); House dust mite allergy; Penicillin allergy; Ragweed allergy.
- Vorgeschichte
- -
- Andere Medikamente
- RHINOCORT [BUDESONIDE]; BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE.]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 30.06.2021
- Beginn
- 28.07.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Fatigue
Gout
Headache
Symptomtext
Gout were off worse; Worse balance; Fatigue level was higher/fatigue; Headache; This spontaneous case was reported by a consumer and describes the occurrence of GOUT (Gout were off worse), BALANCE DISORDER (Worse balance), FATIGUE (Fatigue level was higher/fatigue) and HEADACHE (Headache) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 078C21A and 051C21A) for COVID-19 vaccination. The patient's past medical history included COVID-19 on 22-Mar-2021. Concurrent medical conditions included Multiple sclerosis since 01-Jun-2008. Concomitant products included BACLOFEN, AMPYRA, TAMSULOSIN HYDROCHLORIDE (FLOMAX [TAMSULOSIN HYDROCHLORIDE]), MYRBETRIQ, PROVIGIL, CRESTOR, SINGULAIR, TELMISARTAN, DILTIAZEM, ONGLYZA, ATIVAN, ALBUTEROL, VITAMIN D, CALCIUM, SAW PALMETTO [SERENOA REPENS], METHOTREXATE, RITUXIMAB (RITUXAN) and METHYLPREDNISOLONE SODIUM SUCCINATE (SOLUMEDROL) for an unknown indication. On 30-Jun-2021 at 7:00 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Jul-2021 at 2:30 PM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 28-Jul-2021 at 10:00 PM, the patient experienced GOUT (Gout were off worse), BALANCE DISORDER (Worse balance), FATIGUE (Fatigue level was higher/fatigue) and HEADACHE (Headache). On 30-Jul-2021, GOUT (Gout were off worse), BALANCE DISORDER (Worse balance), FATIGUE (Fatigue level was higher/fatigue) and HEADACHE (Headache) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered GOUT (Gout were off worse), BALANCE DISORDER (Worse balance), FATIGUE (Fatigue level was higher/fatigue) and HEADACHE (Headache) to be possibly related. No treatment information was provided by the reporter. This case was linked to MOD-2021-244820 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Multiple sclerosis.
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19.
- Andere Medikamente
- BACLOFEN; AMPYRA; FLOMAX [TAMSULOSIN HYDROCHLORIDE]; MYRBETRIQ; PROVIGIL; CRESTOR; SINGULAIR; TELMISARTAN; DILTIAZEM; ONGLYZA; ATIVAN; ALBUTEROL; VITAMIN D; CALCIUM; SAW PALMETTO [SERENOA REPENS]; METHOTREXATE; RITUXAN; SOLUMEDROL.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 30.06.2021
- Beginn
- 30.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Vaccination site mass
Symptomtext
it was a bit itchy; small bump that did not grow; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (it was a bit itchy) and VACCINATION SITE MASS (small bump that did not grow) in a 56-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. Concomitant products included LEVOTHYROXINE for an unknown indication. On 30-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Jun-2021, the patient experienced PRURITUS (it was a bit itchy) and VACCINATION SITE MASS (small bump that did not grow). On 13-Jul-2021, PRURITUS (it was a bit itchy) and VACCINATION SITE MASS (small bump that did not grow) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No treatment was reported. This case was linked to MOD-2021-272121 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No Medical History information was reported.
- Andere Medikamente
- LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 13.07.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Headache
Swelling
Urticaria
Vaccination site urticaria
Symptomtext
patient experienced a similar set of hives on the left arm; Hives his right foot, ankle, knee and calf; Red; Swollen; Headache; This spontaneous case was reported by a patient and describes the occurrence of HEADACHE (Headache), URTICARIA (Hives his right foot, ankle, knee and calf), ERYTHEMA (Red), SWELLING (Swollen) and VACCINATION SITE URTICARIA (patient experienced a similar set of hives on the left arm) in a 45-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-Jul-2021, the patient experienced HEADACHE (Headache). On 14-Jul-2021, the patient experienced URTICARIA (Hives his right foot, ankle, knee and calf), ERYTHEMA (Red) and SWELLING (Swollen). On an unknown date, the patient experienced VACCINATION SITE URTICARIA (patient experienced a similar set of hives on the left arm). The patient was treated with IBUPROFEN at an unspecified dose and frequency; HYDROCORTISONE at an unspecified dose and frequency; ALCOHOL at an unspecified dose and frequency and DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at an unspecified dose and frequency. At the time of the report, HEADACHE (Headache), URTICARIA (Hives his right foot, ankle, knee and calf), ERYTHEMA (Red), SWELLING (Swollen) and VACCINATION SITE URTICARIA (patient experienced a similar set of hives on the left arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 17.07.2021
- Beginn
- 25.07.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Vaccination site pain
Vaccination site pruritus
Vaccination site reaction
Vaccination site urticaria
Symptomtext
COVID arm; Itchy; Huge welt; Painful; Fatigue; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE REACTION (COVID arm), VACCINATION SITE PRURITUS (Itchy), VACCINATION SITE URTICARIA (Huge welt), VACCINATION SITE PAIN (Painful) and FATIGUE (Fatigue) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No medical history was provided by the reporter. Concomitant products included CELECOXIB (CELEBREX) and GABAPENTIN for an unknown indication. On 17-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 25-Jul-2021, the patient experienced VACCINATION SITE REACTION (COVID arm), VACCINATION SITE PRURITUS (Itchy), VACCINATION SITE URTICARIA (Huge welt), VACCINATION SITE PAIN (Painful) and FATIGUE (Fatigue). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) on 25-Jul-2021 at a dose of UNK dosage form. At the time of the report, VACCINATION SITE REACTION (COVID arm), VACCINATION SITE PRURITUS (Itchy), VACCINATION SITE URTICARIA (Huge welt), VACCINATION SITE PAIN (Painful) and FATIGUE (Fatigue) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- CELEBREX; GABAPENTIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 20.07.2021
- Beginn
- 20.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Erythema
Fatigue
Myalgia
Pain in extremity
Pruritus
Pyrexia
Symptomtext
pink area that is slightly itchy; pink area that is slightly itchy; Soreness on her arm; fever; fatigue; body ache; stabbing pain in her elbow area after the injection; This spontaneous case was reported by a consumer and describes the occurrence of ERYTHEMA (pink area that is slightly itchy), PRURITUS (pink area that is slightly itchy), PAIN IN EXTREMITY (Soreness on her arm), PYREXIA (fever) and FATIGUE (fatigue) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Blood pressure high. Concomitant products included CLONIDINE for Blood pressure high, ATENOLOL, ACETYLSALICYLIC ACID (BABY ASPIRIN) and SIMVASTATIN for an unknown indication. On 20-Jul-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Jul-2021, the patient experienced PAIN IN EXTREMITY (Soreness on her arm), PYREXIA (fever), FATIGUE (fatigue), MYALGIA (body ache) and ARTHRALGIA (stabbing pain in her elbow area after the injection). On 23-Jul-2021, the patient experienced ERYTHEMA (pink area that is slightly itchy) and PRURITUS (pink area that is slightly itchy). At the time of the report, ERYTHEMA (pink area that is slightly itchy) and PRURITUS (pink area that is slightly itchy) had not resolved and PAIN IN EXTREMITY (Soreness on her arm), PYREXIA (fever), FATIGUE (fatigue), MYALGIA (body ache) and ARTHRALGIA (stabbing pain in her elbow area after the injection) had resolved. Patient was unsure about dose-1 date and bath number. Patient stated that date could be 18 or 22 Jun and the batch number could be 026D21A or 086D21A. She sprayed some alcohol on her arm. Treatment information was not provided. This case was linked to MOD-2021-265327 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood pressure high
- Vorgeschichte
- -
- Andere Medikamente
- ATENOLOL; BABY ASPIRIN; SIMVASTATIN; CLONIDINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 20.07.2021
- Beginn
- 20.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Influenza like illness
Lethargy
Pain in extremity
Symptomtext
pain is on his right leg with a pain scale of 8.5/10; Feels lethargic; Joint pain on right leg; Flu-like symptoms; This spontaneous case was reported by a patient and describes the occurrence of INFLUENZA LIKE ILLNESS (Flu-like symptoms), PAIN IN EXTREMITY (pain is on his right leg with a pain scale of 8.5/10), LETHARGY (Feels lethargic) and ARTHRALGIA (Joint pain on right leg) in a 39-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Jul-2021, the patient experienced INFLUENZA LIKE ILLNESS (Flu-like symptoms), LETHARGY (Feels lethargic) and ARTHRALGIA (Joint pain on right leg). On an unknown date, the patient experienced PAIN IN EXTREMITY (pain is on his right leg with a pain scale of 8.5/10). At the time of the report, INFLUENZA LIKE ILLNESS (Flu-like symptoms), PAIN IN EXTREMITY (pain is on his right leg with a pain scale of 8.5/10), LETHARGY (Feels lethargic) and ARTHRALGIA (Joint pain on right leg) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were provided by reporter. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 08.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Fatigue
Feeling abnormal
Somnolence
Vaccination complication
Symptomtext
Had side effects for 10 days.; has no energy; feels "really down"/ feels like my "blood count is low"; hard to keep her eyes open; feeling tired / fatigued; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (Had side effects for 10 days.), ASTHENIA (has no energy), FEELING ABNORMAL (feels "really down"/ feels like my "blood count is low"), SOMNOLENCE (hard to keep her eyes open) and FATIGUE (feeling tired / fatigued) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VACCINATION COMPLICATION (Had side effects for 10 days.), ASTHENIA (has no energy), FEELING ABNORMAL (feels "really down"/ feels like my "blood count is low"), SOMNOLENCE (hard to keep her eyes open) and FATIGUE (feeling tired / fatigued). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency and MULTIVITAMIN [VITAMINS NOS] at an unspecified dose and frequency. At the time of the report, VACCINATION COMPLICATION (Had side effects for 10 days.), ASTHENIA (has no energy), FEELING ABNORMAL (feels "really down"/ feels like my "blood count is low"), SOMNOLENCE (hard to keep her eyes open) and FATIGUE (feeling tired / fatigued) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 15-Jul-2021: Follow-up information received on 15 Jul 2021 contains updated product information and new events added
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 12.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Vaccination site rash
Symptomtext
hives; developed hives and red blotches around the vaccinated area; This spontaneous case was reported by a consumer and describes the occurrence of URTICARIA (hives) and VACCINATION SITE RASH (developed hives and red blotches around the vaccinated area) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Jul-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced URTICARIA (hives) and VACCINATION SITE RASH (developed hives and red blotches around the vaccinated area). At the time of the report, URTICARIA (hives) and VACCINATION SITE RASH (developed hives and red blotches around the vaccinated area) outcome was unknown. Treatment information not provided. List of concomitant medication were not given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 02.07.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Fatigue
Symptomtext
Cough that doesn?t go away; Feeling tired; This spontaneous case was reported by a patient and describes the occurrence of COUGH (Cough that doesn?t go away) and FATIGUE (Feeling tired) in a 20-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Jul-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Jul-2021, the patient experienced COUGH (Cough that doesn?t go away) and FATIGUE (Feeling tired). The patient was treated with BENZONATATE at an unspecified dose and frequency. At the time of the report, COUGH (Cough that doesn?t go away) and FATIGUE (Feeling tired) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) and mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 06.07.2021
- Beginn
- 07.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Headache
Myalgia
Photophobia
Pyrexia
Vision blurred
Symptomtext
Photophobia; Blurred vision; Fever ranging from 101.6/101.7 degrees Fahrenheit; Body aches; Headaches; This spontaneous case was reported by an other caregiver and describes the occurrence of PHOTOPHOBIA (Photophobia), VISION BLURRED (Blurred vision), PYREXIA (Fever ranging from 101.6/101.7 degrees Fahrenheit), MYALGIA (Body aches) and HEADACHE (Headaches) in a 21-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 07-Jul-2021, the patient experienced PHOTOPHOBIA (Photophobia), VISION BLURRED (Blurred vision), PYREXIA (Fever ranging from 101.6/101.7 degrees Fahrenheit), MYALGIA (Body aches) and HEADACHE (Headaches). The patient was treated with ZINC for Adverse event, at a dose of 1 dosage form; VITAMIN D [VITAMIN D NOS] for Adverse event, at a dose of 1 dosage form and IBUPROFEN (MOTRIN [IBUPROFEN]) for Adverse event, at a dose of 1 dosage form. At the time of the report, PHOTOPHOBIA (Photophobia), VISION BLURRED (Blurred vision), PYREXIA (Fever ranging from 101.6/101.7 degrees Fahrenheit), MYALGIA (Body aches) and HEADACHE (Headaches) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 07-Jul-2021, Body temperature: 101.6/101.7 (High) Fever ranging from 101.6/101.7 degrees Fahrenheit. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant product was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210707; Test Name: Body temperature; Result Unstructured Data: Fever ranging from 101.6/101.7 degrees Fahrenheit
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Erythema
Feeling hot
Pain in extremity
Pruritus
Symptomtext
Red spot on arm tripled in size from shoulder to 6 inches down her arm; Itching on arm; Hot as fire feeling on arm; Bruise; Sore right arm; This spontaneous case was reported by a consumer and describes the occurrence of CONTUSION (Bruise), ERYTHEMA (Red spot on arm tripled in size from shoulder to 6 inches down her arm), PRURITUS (Itching on arm), FEELING HOT (Hot as fire feeling on arm) and PAIN IN EXTREMITY (Sore right arm) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Jun-2021, the patient experienced PAIN IN EXTREMITY (Sore right arm). On 02-Jul-2021, the patient experienced CONTUSION (Bruise). On 05-Jul-2021, the patient experienced ERYTHEMA (Red spot on arm tripled in size from shoulder to 6 inches down her arm), PRURITUS (Itching on arm) and FEELING HOT (Hot as fire feeling on arm). At the time of the report, CONTUSION (Bruise), ERYTHEMA (Red spot on arm tripled in size from shoulder to 6 inches down her arm), PRURITUS (Itching on arm), FEELING HOT (Hot as fire feeling on arm) and PAIN IN EXTREMITY (Sore right arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were provided. Treatment medications included unspecified medicated lotion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 30.06.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nasopharyngitis
Oropharyngeal pain
Symptomtext
Sore throat; Developed a cold; This spontaneous case was reported by a consumer and describes the occurrence of NASOPHARYNGITIS (Developed a cold) and OROPHARYNGEAL PAIN (Sore throat) in a 56-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 30-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Jul-2021, the patient experienced NASOPHARYNGITIS (Developed a cold). On 03-Jul-2021, the patient experienced OROPHARYNGEAL PAIN (Sore throat). On 05-Jul-2021, OROPHARYNGEAL PAIN (Sore throat) had resolved. At the time of the report, NASOPHARYNGITIS (Developed a cold) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant medications were reported. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 30.06.2021
- Beginn
- 30.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
SARS-CoV-2 test
Vaccination site discomfort
Vaccination site pain
Symptomtext
Headache; Fatigue; He reports that he the injection site was bothersome; injection site hurts a little bit; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE DISCOMFORT (He reports that he the injection site was bothersome), VACCINATION SITE PAIN (injection site hurts a little bit), HEADACHE (Headache) and FATIGUE (Fatigue) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The patient's past medical history included COVID-19 on 22-Mar-2021. Concurrent medical conditions included Multiple sclerosis (worst balance, fatigue ,gait. Received a monoclonal antibody treatment in March of 2021.) since 06-Jan-2008. Concomitant products included FAMPRIDINE (AMPYRA), MODAFINIL (PROVIGIL [MODAFINIL]), MORNIFLUMATE (FLOMAX [MORNIFLUMATE]), BACLOFEN, TELMISARTAN, DILTIAZEM, METHOTREXATE SODIUM (METHOTREXATE INJECTION BP), METHYLPREDNISOLONE SODIUM SUCCINATE (SOLUMEDROL), MIRABEGRON (MYRBETRIQ), ROSUVASTATIN CALCIUM (CRESTOR), MONTELUKAST SODIUM (SINGULAIR), SAXAGLIPTIN HYDROCHLORIDE (ONGLYZA [SAXAGLIPTIN HYDROCHLORIDE]), LORAZEPAM (ATIVAN), ALBUTEROL [SALBUTAMOL], VITAMIN D [VITAMIN D NOS], CALCIUM, SERENOA REPENS FRUIT (SAW PALMETTO [SERENOA REPENS FRUIT]) and RITUXIMAB (RITUXAN) for an unknown indication. On 30-Jun-2021 at 7:00 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Jun-2021, the patient experienced VACCINATION SITE DISCOMFORT (He reports that he the injection site was bothersome) and VACCINATION SITE PAIN (injection site hurts a little bit). On 30-Jun-2021 at 10:00 PM, the patient experienced HEADACHE (Headache) and FATIGUE (Fatigue). On 01-Jul-2021, HEADACHE (Headache) and FATIGUE (Fatigue) had resolved. At the time of the report, VACCINATION SITE DISCOMFORT (He reports that he the injection site was bothersome) and VACCINATION SITE PAIN (injection site hurts a little bit) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 22-Mar-2021, SARS-CoV-2 test: positive (Positive) Positive. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. Patient took dose 2 on 28-Jul-2021. No treatment information was provided by the reporter. This case was linked to MOD-2021-272092 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 30-Jul-2021: Added patient demographic, added medical history, added lab data, added dose 2 details, updated concomitant medication details, added event fatigue and updated event outcome.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210322; Test Name: COVID-19 test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Multiple sclerosis (worst balance, fatigue ,gait. Received a monoclonal antibody treatment in March of 2021.)
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- AMPYRA; PROVIGIL [MODAFINIL]; FLOMAX [MORNIFLUMATE]; BACLOFEN; TELMISARTAN; DILTIAZEM; METHOTREXATE INJECTION BP; SOLUMEDROL; MYRBETRIQ; CRESTOR; SINGULAIR; ONGLYZA [SAXAGLIPTIN HYDROCHLORIDE]; ATIVAN; ALBUTEROL [SALBUTAMOL]; VITAMIN D [VIT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 26.08.2021
- Beginn
- 26.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Erythema
Malaise
Pain
Peripheral swelling
Symptomtext
Swollen, red arm, aching ,chills, not feeling well, and lasted 48 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 25.06.2021
- Beginn
- 08.01.2022
- Tage bis Beginn
- 197,0
- Dosis
- 2
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal discomfort
Abdominal pain upper
COVID-19
Chest X-ray normal
Haematemesis
Cold sweat
Diarrhoea
Muscle spasms
Pain in extremity
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Vomiting
Symptomtext
Covid19 breakthrough. 1st Vaccine on 05/28/2021. 35 y/o with PMH presents to Ed with c/o vomiting bright red blood and an uneasy stomach. Later vomited coffee ground emesis and had pain in upper mid abdomen. Pt with low grade fevers, O2 sat room air 100% and CXR unremarkable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- SARS CoV 2 PCR Covid19- Detected 01/08/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ETOH abuse, HTN, Tachycardia
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 25.06.2021
- Beginn
- 08.01.2022
- Tage bis Beginn
- 197,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal discomfort
Abdominal pain upper
COVID-19
Chest X-ray normal
Haematemesis
Cold sweat
Diarrhoea
Muscle spasms
Pain in extremity
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Vomiting
Symptomtext
Covid19 breakthrough. 1st Vaccine on 05/28/2021. 35 y/o with PMH presents to Ed with c/o vomiting bright red blood and an uneasy stomach. Later vomited coffee ground emesis and had pain in upper mid abdomen. Pt with low grade fevers, O2 sat room air 100% and CXR unremarkable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- SARS CoV 2 PCR Covid19- Detected 01/08/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ETOH abuse, HTN, Tachycardia
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 28.07.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 18,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fungal test
Genital rash
Psoriasis
Rash
Rash papular
Rash pruritic
Rash pustular
Symptomtext
Ist shot on 7-28-21, 2nd on 8-25-21. Rash from hell in my pubic area back to butt cheeks. Don't recall whether it started between the two shots or shortly after the 2nd. First sign was itching, then rash. Have one small spot of psoriasis on ankle so thought it might be that so treated with MG217 that keeps my ankle psoriasis in check, no response. Extremely itchy and if scratched, feels bumpy under skin, then oozes almost clear, somewhat sticky substance, like when one has a severe sunburn that blisters and there's watery substance under the blister. Finally tried diluted vinegar wipe about the time I made appt with Clinic. It relieved the itch. Then applied A&D ointment or cream to area. NP at Clinic tested for yeast/fungus, negative but gave me a script for Fluconazole and psoriasis tar treatment. I got the Fluconazole and took it. Rash may be improving, still using vinegar and A&D.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Genital rash
- Hospital-Tage
- -
- Labordaten
- 12-9-21 yeast
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- multi vitamin, 80mg aspirin, cranberry capsule, vit D
- Allergien
- sulfa, latex
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 09.07.2021
- Beginn
- 27.08.2021
- Tage bis Beginn
- 49,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blister
Herpes zoster
Pain
Post herpetic neuralgia
Rash
Symptomtext
I developed Shingles shortly after my second dose of the Moderna vaccine and had to be treated with medication to try to lessen the outbreak of blisters and pain. My rash gradually went away but I still have postherpetic neuralgia pain to this day. I believe the Moderna vaccine triggered my Shingles outbreak. I never had Shingles prior to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Rosuvastatin, CoQ10, Vitamin D3
- Allergien
- Vytorin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 10.07.2021
- Beginn
- 10.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site pain
Symptomtext
Patient experienced a sore left arm; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (Patient experienced a sore left arm) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Jul-2021, the patient experienced VACCINATION SITE PAIN (Patient experienced a sore left arm). At the time of the report, VACCINATION SITE PAIN (Patient experienced a sore left arm) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. No relevant concomitant medications were reported. No treatment information was provided. This case was linked to MOD-2021-405045 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 10.07.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 27,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Headache
Insomnia
Malaise
Myalgia
Nausea
Symptomtext
Did not feel good into sunday; Nauseous; Headache; Body ache; Woke up Saturday feeling sick; The patient did not sleep all night, It was like drank 20 cups of coffee, It was like brain was racing; This spontaneous case was reported by a non-health professional and describes the occurrence of INSOMNIA (The patient did not sleep all night, It was like drank 20 cups of coffee, It was like brain was racing), MALAISE (Woke up Saturday feeling sick), FEELING ABNORMAL (Did not feel good into sunday), NAUSEA (Nauseous) and HEADACHE (Headache) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 052C21A and 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 10-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 06-Aug-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced INSOMNIA (The patient did not sleep all night, It was like drank 20 cups of coffee, It was like brain was racing). On 07-Aug-2021, the patient experienced MALAISE (Woke up Saturday feeling sick), NAUSEA (Nauseous), HEADACHE (Headache) and MYALGIA (Body ache). On 08-Aug-2021, the patient experienced FEELING ABNORMAL (Did not feel good into sunday). At the time of the report, INSOMNIA (The patient did not sleep all night, It was like drank 20 cups of coffee, It was like brain was racing), MALAISE (Woke up Saturday feeling sick), FEELING ABNORMAL (Did not feel good into sunday), NAUSEA (Nauseous), HEADACHE (Headache) and MYALGIA (Body ache) outcome was unknown. No concomitant product use was provided by the reporter. No treatment medication was provided. This case was linked to MOD-2021-405040 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 23.11.2021
- Impfdatum
- 11.03.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 244,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Fatigue
SARS-CoV-2 test positive
Symptomtext
11/10/21 presents to EC ED for "weakness and fatigue". PMH "heart transplant recipient, diabetes type 2, HTN, CAD s/p PCI, CHF, pulmonary embolism on Xarelto and COVID + on 11/01/21"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 11/10/21 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- 14.07.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Audiogram abnormal
Balance disorder
Cochlea implant
Deafness neurosensory
Deafness unilateral
Dizziness
Middle ear effusion
Tinnitus
Symptomtext
I had received my first shot of the Moderna vaccine on July 14, 2021 sometime in the afternoon. I woke up on July 15, 2021 and felt a sense of imbalance during the day along with some dizziness. I woke up on the morning of July 16, 2021 and I experienced complete hearing loss in my left ear. I was also experiencing a loud ringing noise in my left ear. I figured it was just allergies or some side effect from the vaccine since I heard that some people may experience COVID-related symptoms after receiving the first or second dose. Several days passed as I assumed my hearing would just come back in my left ear, but about a week later I went to the doctors to get it checked it. When I went there, the nurse practitioner told me that it was just allergies and I must have fluid in my ear. They told me I had tinnitus and they prescribed me Claritin-D and told me my hearing would come back in less than two weeks. They said if my hearing in my left ear didn't come back in two weeks or less that I should schedule another appointment. Two weeks went by and my hearing never came back. The ability to listen to others became exceptionally difficult since I am only able to hear from my right ear now. This started becoming serious to me and I became very worried. I realized that this might be something serious. I went back to the doctors and saw another nurse practitioner who told me to just wait for the "fluid in my ear" to clear out and continue taking the Claritin-D daily. A few weeks later I talked to a friend about my problem. She referred me to an ears nose and throat specialist, so I made an appointment with an ENT doctor. I went to this appointment two weeks later and the doctor performed some sound tests. She informed me that I had nerve damage in my left ear and that my ability to hear from my left ear again is impossible since my cochlea was somehow permanently damaged. She explained that the only way I could hear from my left ear again is by receiving cochlear implants. She also explained that this is a medical mystery to her since there are no possible causes of this happening. She explained that complete nerve damage in the cochlea only happens from a viral infection or trauma to the ear or head, none of which I had experienced leading up to this condition. I have no prior head or ear injuries that could have caused this. I never contracted COVID-19 or any other virus in the year of 2021 or during the weeks and months leading up to the date of losing the hearing in my left ear. I also have no health conditions that could have caused this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- I received a hearing aid medical clearance form from the ENT doctor. My ENT doctor performed an audiogram test on me. She wrote "Reports sudden hearing loss of left ear two months ago. Has tinnitus. Reliability: good". The audiogram showed that I have severe to profound hearing loss in my left ear, while my right ear has normal and healthy hearing function.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- IC SERTRALINE HCL 100 MG TABLET
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 24.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Chills
Discomfort
Dysuria
Feeling abnormal
Pain
Pyrexia
Urinary tract infection
Symptomtext
I started with low grade temp and fever 7 hrs after, then at 4 the next day I had a backache which began in my lower back and began moving up, and symptoms of a uti despite taking motrin and Tylenol. I had pressure in my lower region, pain and especially during urinating, and chills, with a temp in the evening. I called my dr the next day because I was feeling worse and the motrin and Tylenol weren't helping. I was prescribed ciproflxacin 250 mg and phenazopyridine 100 MG. Yesterday after 4 days on meds, I'm feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- My dr visit was a Tele visit bc I couldn't get seen before the office closed.
- Aktuelle Erkrankungen
- Had a flu vaccine 3 weeks prior and a head cold two weeks before that I had tested negative for covid at the time I fell ill.
- Vorgeschichte
- Hashimotos thyroid.
- Andere Medikamente
- Levothyroxine
- Allergien
- Penicillin.
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 21.10.2021
- Impfdatum
- 06.05.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 68,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Abdominal pain lower
Biopsy liver
Cholangitis
Gallbladder disorder
Hepatic enzyme increased
Hepatobiliary scan
Laboratory test
Malaise
Pyrexia
Symptomtext
Was very sick for both immunizations for about 24 hours. On July 14th began with fever and right lower quadrant pain. Went to Emergency room on the 16th of July with highly elevated liver enzymes, low grade fever, inflamed bile ducts. Possible Gall bladder infection. Was admitted on July 16th. HIda scan showed no gall bladder filling. I have had numerous testing , biopsies. a Repeat HIDA scan shows gallbladder now filling. I remain not feeling well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain lower
- Hospital-Tage
- 2,0
- Labordaten
- liver enzymes, liver biopsy, two Hida Scans, Hospitalization, tooo numerous to count.
- Aktuelle Erkrankungen
- None, had Covid in 1/2021 and was admitted into hospital for it.
- Vorgeschichte
- Childhood cancer in 1968 with removal of right kidney and chemo. and radiation.
- Andere Medikamente
- synthroid, Lipitor, Avapro, Prozac, ultraam, Zanaflex
- Allergien
- NSAIDS,
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 19.10.2021
- Impfdatum
- 18.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chest discomfort
Pain in extremity
Peripheral swelling
Vaccination complication
Vaccination site pain
Symptomtext
The 2 toes next to the baby toe on his left foot swelled up; The finger next to the pinkie on his left hand swelled too and is painful,he can't bend it; He has throbbing in the joints of that finger, and it sometimes wakes him up; Chest discomfort from the center of the chest over to the left side of the chest; This thing with the shot is really irritating; Sharp pain in his left shoulder; Left arm hurt & was sore; This spontaneous case was reported by a consumer and describes the occurrence of PERIPHERAL SWELLING (The 2 toes next to the baby toe on his left foot swelled up), PERIPHERAL SWELLING (The finger next to the pinkie on his left hand swelled too and is painful,he can't bend it), PAIN IN EXTREMITY (He has throbbing in the joints of that finger, and it sometimes wakes him up), CHEST DISCOMFORT (Chest discomfort from the center of the chest over to the left side of the chest) and VACCINATION COMPLICATION (This thing with the shot is really irritating) in a 62-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 18-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PERIPHERAL SWELLING (The 2 toes next to the baby toe on his left foot swelled up), PERIPHERAL SWELLING (The finger next to the pinkie on his left hand swelled too and is painful,he can't bend it), PAIN IN EXTREMITY (He has throbbing in the joints of that finger, and it sometimes wakes him up), CHEST DISCOMFORT (Chest discomfort from the center of the chest over to the left side of the chest), VACCINATION COMPLICATION (This thing with the shot is really irritating), ARTHRALGIA (Sharp pain in his left shoulder) and VACCINATION SITE PAIN (Left arm hurt & was sore). At the time of the report, PERIPHERAL SWELLING (The 2 toes next to the baby toe on his left foot swelled up), PERIPHERAL SWELLING (The finger next to the pinkie on his left hand swelled too and is painful,he can't bend it), PAIN IN EXTREMITY (He has throbbing in the joints of that finger, and it sometimes wakes him up), CHEST DISCOMFORT (Chest discomfort from the center of the chest over to the left side of the chest), VACCINATION COMPLICATION (This thing with the shot is really irritating) and ARTHRALGIA (Sharp pain in his left shoulder) outcome was unknown and VACCINATION SITE PAIN (Left arm hurt & was sore) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided by the reporter. This case was linked to MOD-2021-347048 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 12-Oct-2021: Event -Vaccination complication was added and also Vaccination Facility details were added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 18.10.2021
- Impfdatum
- 18.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Chest discomfort
Pain in extremity
Peripheral swelling
Vaccination complication
Symptomtext
Chest discomfort from the center of the chest over to the left side of the chest; The finger next to the pinkie on his left hand swelled too and is painful, he can't bend it, he has throbbing in the joints of that finger, and it sometimes wakes him up; then the 2 toes next to the baby toe on his left foot swelled up, then the finger next to the pinkie on his left hand swelled too; this thing with the shot is really irritating me, it goes on and on; Sharp pain in his left shoulder; This spontaneous case was reported by a consumer and describes the occurrence of CHEST DISCOMFORT (Chest discomfort from the center of the chest over to the left side of the chest), PAIN IN EXTREMITY (The finger next to the pinkie on his left hand swelled too and is painful, he can't bend it, he has throbbing in the joints of that finger, and it sometimes wakes him up), PERIPHERAL SWELLING (then the 2 toes next to the baby toe on his left foot swelled up, then the finger next to the pinkie on his left hand swelled too), VACCINATION COMPLICATION (this thing with the shot is really irritating me, it goes on and on) and ARTHRALGIA (Sharp pain in his left shoulder) in a 62-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced CHEST DISCOMFORT (Chest discomfort from the center of the chest over to the left side of the chest), PAIN IN EXTREMITY (The finger next to the pinkie on his left hand swelled too and is painful, he can't bend it, he has throbbing in the joints of that finger, and it sometimes wakes him up), PERIPHERAL SWELLING (then the 2 toes next to the baby toe on his left foot swelled up, then the finger next to the pinkie on his left hand swelled too), VACCINATION COMPLICATION (this thing with the shot is really irritating me, it goes on and on) and ARTHRALGIA (Sharp pain in his left shoulder). At the time of the report, CHEST DISCOMFORT (Chest discomfort from the center of the chest over to the left side of the chest), PAIN IN EXTREMITY (The finger next to the pinkie on his left hand swelled too and is painful, he can't bend it, he has throbbing in the joints of that finger, and it sometimes wakes him up), PERIPHERAL SWELLING (then the 2 toes next to the baby toe on his left foot swelled up, then the finger next to the pinkie on his left hand swelled too) and ARTHRALGIA (Sharp pain in his left shoulder) had not resolved and VACCINATION COMPLICATION (this thing with the shot is really irritating me, it goes on and on) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment medications were reported. It was reported that, about a month and a half ago he began having reactions. He never had tested positive for Covid, never had symptoms like this before. Patient had not history of myocarditis or pericarditis This case was linked to MOD-2021-346533 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 12-Oct-2021: Follow up added New reporter, vaccine facility info and event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 07.10.2021
- Impfdatum
- 25.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Inappropriate schedule of product administration
Memory impairment
Myalgia
Pyrexia
Symptomtext
No recollection of what had happened during the past 12 hours; 2nd dose 6 weeks after the first dose; Fever; Fatigue; Achy symptoms; This spontaneous case was reported by a consumer and describes the occurrence of MEMORY IMPAIRMENT (No recollection of what had happened during the past 12 hours), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose 6 weeks after the first dose), PYREXIA (Fever), FATIGUE (Fatigue) and MYALGIA (Achy symptoms) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The patient's past medical history included COVID-19 in October 2020, Clot blood (Patient was hospitalized for 7 days (discharged on 02Nov2021) because of a blood clot in the lung.) from October 2020 to November 2020 and Weight loss. Concurrent medical conditions included Neurological disorder NOS (neurological ones, as she said COVID affected her spine and has problems with coordination.). On 25-Jun-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Jun-2021, the patient experienced MEMORY IMPAIRMENT (No recollection of what had happened during the past 12 hours), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose 6 weeks after the first dose), PYREXIA (Fever), FATIGUE (Fatigue) and MYALGIA (Achy symptoms). On 25-Jun-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose 6 weeks after the first dose) had resolved. At the time of the report, MEMORY IMPAIRMENT (No recollection of what had happened during the past 12 hours) had resolved and PYREXIA (Fever), FATIGUE (Fatigue) and MYALGIA (Achy symptoms) outcome was unknown. No concomitant medication was reported. No treatment medication was reported. The patient had no recollection of what had happened during the past 12 hours what day it was and had to call her daughter. It took a couple days to clear it all out. This case was linked to MOD-2021-335144 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Clot blood (Patient was hospitalized for 7 days (discharged on 02Nov2021) because of a blood clot in the lung.); COVID-19; Neurological disorder NOS (neurological ones, as she said COVID affected her spine and has problems with coordination.); Weight loss
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 23.06.2021
- Beginn
- 20.07.2021
- Tage bis Beginn
- 27,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site mass
Limb discomfort
Symptomtext
Lump on Arm near injection sight of 2nd Moderna Covid 19 vaccination that appeared approximately 30 days after 2nd injection. While the arm does not feel like Covid Arm, each day it feels like I have had a shot given to me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site mass
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Thyroid
- Andere Medikamente
- Zyrtec, Vitamin D, Lexapro, Losartin, Levythyroxine
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 23.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Fatigue
Headache
Lymphadenopathy
Myalgia
Nausea
Pyrexia
Somnolence
Tenderness
Vaccination complication
Symptomtext
Nauseous; Didn't feel good; Body ache; Tiredness / Felt tired / Tired; Headache; Dizziness / Dizzy; Tenderness in lymph gland in right armpit / swollen lymph gland; Tenderness extends down the right side to waist; Couldn't keep my eyes open; Chilled; Fever; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (Dizziness / Dizzy), TENDERNESS (Tenderness extends down the right side to waist), SOMNOLENCE (Couldn't keep my eyes open), VACCINATION COMPLICATION (Didn't feel good) and MYALGIA (Body ache) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 053E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Allergy to metals (Sulfur), Food allergy (MSG) and Hypothyroidism since 1990. Concomitant products included LEVOTHYROXINE SODIUM (SYNTHROID) for Hypothyroidism. On 23-Jul-2021 at 10:00 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Aug-2021 at 11:00 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 23-Jul-2021, the patient experienced TENDERNESS (Tenderness extends down the right side to waist). 23-Jul-2021, the patient experienced SOMNOLENCE (Couldn't keep my eyes open), CHILLS (Chilled) and PYREXIA (Fever). On 23-Jul-2021 at 11:00 AM, the patient experienced DIZZINESS (Dizziness / Dizzy). 23-Jul-2021 at 11:00 AM, the patient experienced LYMPHADENOPATHY (Tenderness in lymph gland in right armpit / swollen lymph gland). On 23-Jul-2021 at 1:00 PM, the patient experienced MYALGIA (Body ache). 23-Jul-2021 at 1:00 PM, the patient experienced FATIGUE (Tiredness / Felt tired / Tired) and HEADACHE (Headache). On 24-Jul-2021, the patient experienced VACCINATION COMPLICATION (Didn't feel good). On 25-Jul-2021, the patient experienced NAUSEA (Nauseous). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency; ELECTROLYTES NOS, GLUCOSE (PEDIALYTE [ELECTROLYTES NOS;GLUCOSE]) for Adverse event, at a dose of 12 ounces daily; ECHINACEA ANGUSTIFOLIA ROOT, ECHINACEA PURPUREA ROOT (ECHINACEA 2000+) for Adverse event, at an unspecified dose and frequency and ZINC for Adverse event, at an unspecified dose and frequency. On 28-Jul-2021, MYALGIA (Body ache), FATIGUE (Tiredness / Felt tired / Tired) and HEADACHE (Headache) had resolved. On 12-Aug-2021, DIZZINESS (Dizziness / Dizzy) and LYMPHADENOPATHY (Tenderness in lymph gland in right armpit / swollen lymph gland) had resolved. At the time of the report, TENDERNESS (Tenderness extends down the right side to waist), SOMNOLENCE (Couldn't keep my eyes open), CHILLS (Chilled) and PYREXIA (Fever) outcome was unknown and VACCINATION COMPLICATION (Didn't feel good) and NAUSEA (Nauseous) had resolved. Patient reports that they believe they may have had COVID in DEC2019 but at the time there was no test and they did not get tested but was sick for 3-4 weeks. Most recent FOLLOW-UP information incorporated above includes: On 28-Sep-2021: Follow up received on 28 sep 2021 has significant information which contains medical history, second dose information updated, events added, and outcome updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to metals (Sulfur); Food allergy (MSG); Hypothyroidism
- Vorgeschichte
- -
- Andere Medikamente
- SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 28.09.2021
- Impfdatum
- 20.08.2021
- Beginn
- 19.09.2021
- Tage bis Beginn
- 30,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Lymph node pain
Lymphadenopathy
Vaccination site pain
Symptomtext
Arm pain; Headache; Lymph node on right side of collar bone swell up; Lymph node on right side of collar bone painful; This spontaneous case was reported by a consumer and describes the occurrence of LYMPHADENOPATHY (Lymph node on right side of collar bone swell up), LYMPH NODE PAIN (Lymph node on right side of collar bone painful), VACCINATION SITE PAIN (Arm pain) and HEADACHE (Headache) in a 34-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 19-Sep-2021, the patient experienced LYMPHADENOPATHY (Lymph node on right side of collar bone swell up) and LYMPH NODE PAIN (Lymph node on right side of collar bone painful). On an unknown date, the patient experienced VACCINATION SITE PAIN (Arm pain) and HEADACHE (Headache). The patient was treated with ASPIRIN [ACETYLSALICYLIC ACID] at a dose of UNK dosage form; IBUPROFEN at a dose of UNK dosage form and HYDROCODONE at a dose of UNK dosage form. At the time of the report, LYMPHADENOPATHY (Lymph node on right side of collar bone swell up), LYMPH NODE PAIN (Lymph node on right side of collar bone painful), VACCINATION SITE PAIN (Arm pain) and HEADACHE (Headache) outcome was unknown. No relevant concomitant medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 24.09.2021
- Impfdatum
- 12.06.2021
- Beginn
- 19.06.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blood test
Electromyogram
Influenza like illness
Injection site pain
Laboratory test
Myalgia
Nerve conduction studies
Neuropathy peripheral
Pain
Pyrexia
Small fibre neuropathy
Symptomtext
Dose 1: a - muscular pain in shot location 2 days following administration of vaccine. Dose 2: a - muscular pain in shot location 2 days following administration of vaccine. b - Flu like symptoms for three days following vaccine - mild fever, body aches, muscles soreness in legs. c - Small fiber peripheral neuropathy in feet - has gradually advance to arms, legs and trunk of body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Labs - blood - 2021_07_30 Labs - blood - 2021_08_18 Nerve conduction test (EMG) - 2021_09_09 Diagnosis - Idiopathic Small Fiber Peripheral Neuropathy.
- Aktuelle Erkrankungen
- Injury: Cervical neck form overuse playing tennis. No structural damage, resolving with physical therarpy. Illness: reaction from 2nd Moderna vaccine - flu like symptoms for three days.
- Vorgeschichte
- Anxiety.
- Andere Medikamente
- No prescriptions: Supplements: Curamin Extra Strength (Terry Naturals), Thyro Complex (Endo-met), Osteo Bi-Flex Triple Strength, Paramin (Endo-met), Endo A-C (Endo-Met), Megapan (Endo-Met), Zinc (endo-met). Herbal remedies: None
- Allergien
- Levaquin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 23.09.2021
- Impfdatum
- 01.07.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 39,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Pain
Trigeminal neuralgia
Symptomtext
Trigeminal neuralgia flare up; Extremely Bad pain; Inappropriate schedule of vaccine administered; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (Extremely Bad pain), TRIGEMINAL NEURALGIA (Trigeminal neuralgia flare up) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 052E21A and 051C21A) for COVID-19 vaccination. The patient's past medical history included Chronic kidney disease stage 3 in 2008, Microvascular decompression (05/2019 and 12/2020: first and second failed microvascular decompression surgeries.) in May 2019 and Microvascular decompression in December 2020. Concurrent medical conditions included Trigeminal neuralgia (Became bilateral on 07/19/2021) since 2019. Concomitant products included CARBAMAZEPINE (TEGRETOL) from 09-Jan-2019 to an unknown date for Trigeminal neuralgia. On 01-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 09-Aug-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). On 12-Aug-2021, the patient experienced PAIN (Extremely Bad pain). On 20-Aug-2021, the patient experienced TRIGEMINAL NEURALGIA (Trigeminal neuralgia flare up). On 22-Aug-2021, TRIGEMINAL NEURALGIA (Trigeminal neuralgia flare up) had resolved. At the time of the report, PAIN (Extremely Bad pain) outcome was unknown and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. No treatment medication reported. patient also added that extremely bad pain,on 08/12, 14, 15, 18, 19 but not quite "flare up level," This case was linked to MOD-2021-277719 (Patient Link). Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Trigeminal neuralgia (Became bilateral on 07/19/2021)
- Vorgeschichte
- Medical History/Concurrent Conditions: Chronic kidney disease stage 3; Microvascular decompression (05/2019 and 12/2020: first and second failed microvascular decompression surgeries.); Microvascular decompression
- Andere Medikamente
- TEGRETOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 23.09.2021
- Impfdatum
- 21.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Hypokinesia
Symptomtext
Can't lift it up parallel without shooting pain; Shoulder just hurts/can't lift it up parallel without shooting pain/ My left shoulder is still in pain; This spontaneous case was reported by a consumer and describes the occurrence of HYPOKINESIA (Can't lift it up parallel without shooting pain) and ARTHRALGIA (Shoulder just hurts/can't lift it up parallel without shooting pain/ My left shoulder is still in pain) in a 49-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 017E21A and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 21-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient experienced HYPOKINESIA (Can't lift it up parallel without shooting pain) and ARTHRALGIA (Shoulder just hurts/can't lift it up parallel without shooting pain/ My left shoulder is still in pain). At the time of the report, HYPOKINESIA (Can't lift it up parallel without shooting pain) and ARTHRALGIA (Shoulder just hurts/can't lift it up parallel without shooting pain/ My left shoulder is still in pain) had not resolved. No concomitant medication was provided by reporter. No treatment information was provided by reporter. This case was linked to MOD-2021-318973 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 16-Sep-2021: Follow up received: Outcome of the event updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 22.09.2021
- Impfdatum
- 21.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Myalgia
Symptomtext
He states his shoulder pain started with the first shot.; His shoulder was sore, like a Charlie's horse; This spontaneous case was reported by a consumer and describes the occurrence of ARTHRALGIA (He states his shoulder pain started with the first shot.) and MYALGIA (His shoulder was sore, like a Charlie's horse) in a 49-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 017E21A) for COVID-19 vaccination. No Medical History information was reported. On 21-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced ARTHRALGIA (He states his shoulder pain started with the first shot.) and MYALGIA (His shoulder was sore, like a Charlie's horse). At the time of the report, ARTHRALGIA (He states his shoulder pain started with the first shot.) and MYALGIA (His shoulder was sore, like a Charlie's horse) outcome was unknown. No concomitant medications reported. No treatment medications reported. This case was linked to MOD-2021-319007 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 22.09.2021
- Impfdatum
- 12.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Malaise
Product dose omission issue
Tooth infection
Symptomtext
felt sick; tooth infection; Product dose omission issue; This spontaneous case was reported by a pharmacist and describes the occurrence of MALAISE (felt sick), TOOTH INFECTION (tooth infection) and PRODUCT DOSE OMISSION ISSUE (Product dose omission issue) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced MALAISE (felt sick), TOOTH INFECTION (tooth infection) and PRODUCT DOSE OMISSION ISSUE (Product dose omission issue). The patient was treated with AMOXICILLIN, CLAVULANIC ACID (AUGMENTINE [AMOXICILLIN;CLAVULANIC ACID]) ongoing since an unknown date for Tooth infection, at a dose of 1 dosage form. At the time of the report, MALAISE (felt sick) and TOOTH INFECTION (tooth infection) outcome was unknown and PRODUCT DOSE OMISSION ISSUE (Product dose omission issue) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant information were reported by the reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 17.09.2021
- Impfdatum
- 20.07.2021
- Beginn
- 21.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Symptomtext
sore arm; This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (sore arm) in a 56-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 17-aug-21) for COVID-19 vaccination. No Medical History information was reported. On 20-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Aug-2021, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 21-Jul-2021, the patient experienced MYALGIA (sore arm). At the time of the report, MYALGIA (sore arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product was not provided by the reporter Treatment information was not provided This case was linked to MOD-2021-305779 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 30.06.2021
- Beginn
- 30.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling hot
Nerve conduction studies
Pain in extremity
Peripheral swelling
Product dose omission issue
Pyrexia
Swelling
Vaccination site erythema
Vaccination site swelling
Vaccination site warmth
Symptomtext
Pain in arm for days; Left arm swelled; The vaccination site is swollen, red, and heat; Vaccination site is swollen; Redness of left arm vaccination site; Carrying a low grade fever had 100.7 at ear, 99 is a fever for me"; Patient advised by her doctor to not get the second vaccine as my allergic reaction would be worse; Feeling hot; The patient noticed her face, lips, eyes and tongue were selling up fast; This case was initially received via an unknown source (no reference has been entered for a health authority or license partner) on 08-Jul-2021. The most recent information was received on 31-Aug-2021 and was forwarded to Moderna on 31-Aug-2021. This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Pain in arm for days), PERIPHERAL SWELLING (Left arm swelled), VACCINATION SITE WARMTH (The vaccination site is swollen, red, and heat), FEELING HOT (Feeling hot) and SWELLING (The patient noticed her face, lips, eyes and tongue were selling up fast) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Drug allergy (sulfa allergy.), Drug allergy (Levaquin allergy.), Allergy to antibiotic (antibiotics allergy.), Allergy to antibiotic (tetracycline allergy.), Drug allergy (codeine allergy.), Chiari malformation, Mast cell activation syndrome, Dysautonomia since 12-Oct-2018, Syncope vasovagal since 12-Oct-2018, Mast cell activation syndrome (On 6-30-2021 the mast cell activation syndrome got worsen with vaccine.) since October 2018, Hypertension (Improved with meds.), Hypotension (Improved with meds), High cholesterol (Improved with treatment.), Mitral valve prolapse, Drug allergy, Allergy to antibiotic, Allergy to antibiotic, Drug allergy, Drug allergy, Allergy to chemicals and Allergy to vaccine. Concomitant products included ROSUVASTATIN CALCIUM (CRESTOR) for Blood cholesterol increased, ROSUVASTATIN CALCIUM (ROSUVASTATIN +PHARMA) for Cholesterol, LISINOPRIL for Hypertension, FISH OIL (FISH OIL OMEGA 3) for Triglycerides, VITAMIN B12 NOS and COLECALCIFEROL (VITAMIN D3) for an unknown indication. On 30-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Jun-2021, the patient experienced FEELING HOT (Feeling hot) and SWELLING (The patient noticed her face, lips, eyes and tongue were selling up fast). On an unknown date, the patient experienced PAIN IN EXTREMITY (Pain in arm for days), PERIPHERAL SWELLING (Left arm swelled), VACCINATION SITE WARMTH (The vaccination site is swollen, red, and heat), VACCINATION SITE SWELLING (Vaccination site is swollen), VACCINATION SITE ERYTHEMA (Redness of left arm vaccination site), PYREXIA (Carrying a low grade fever had 100.7 at ear, 99 is a fever for me") and PRODUCT DOSE OMISSION ISSUE (Patient advised by her doctor to not get the second vaccine as my allergic reaction would be worse). The patient was treated with PARACETAMOL (TYLENOL) for Pain, at a dose of 1 dosage form; LORATADINE, PSEUDOEPHEDRINE HYDROCHLORIDE (BENADRYL 24 D) for Swelling, at a dose of 50 mg and PREDNISONE for Fever, at an unspecified dose and frequency. On 15-Jul-2021, FEELING HOT (Feeling hot) and SWELLING (The patient noticed her face, lips, eyes and tongue were selling up fast) had resolved. At the time of the report, PAIN IN EXTREMITY (Pain in arm for days), PERIPHERAL SWELLING (Left arm swelled), VACCINATION SITE WARMTH (The vaccination site is swollen, red, and heat), VACCINATION SITE SWELLING (Vaccination site is swollen), VACCINATION SITE ERYTHEMA (Redness of left arm vaccination site) and PYREXIA (Carrying a low grade fever had 100.7 at ear, 99 is a fever for me") outcome was unknown and PRODUCT DOSE OMISSION ISSUE (Patient advised by her doctor to not get the second vaccine as my allergic reaction would be worse) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Nerve conduction studies: abnormal (abnormal) unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment medications include ice. The concomitant medication included omega 3 ethyl esters. The patient stayed well hydrated for a few days with no improvement. Patient was treated with prednisone for 6 days for fever which helped. Most recent FOLLOW-UP information incorporated above includes: On 31-Aug-2021: significant follow up : included patient details and medical history. New events and concomitant medications were added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Name: Nerve conduction studies; Result Unstructured Data: unknown
- Aktuelle Erkrankungen
- Allergy to antibiotic (tetracycline allergy.); Allergy to antibiotic (antibiotics allergy.); Allergy to antibiotic; Allergy to chemicals; Allergy to vaccine; Chiari malformation; Drug allergy (sulfa allergy.); Drug allergy (Levaquin allergy.); Drug allergy (codeine allergy.); Drug allergy; Dysautonomia; High cholesterol (Improved with treatment.); Hypertension (Improved with meds.); Hypotension (Improved with meds); Mast cell activation syndrome (On 6-30-2021 the mast cell activation syndrome got worsen with vaccine.); Mast cell activation syndrome; Mitral valve prolapse; Syncope vasovagal
- Vorgeschichte
- -
- Andere Medikamente
- LISINOPRIL; CRESTOR; VITAMIN B12 NOS; VITAMIN D3; FISH OIL OMEGA 3; ROSUVASTATIN +PHARMA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 16.09.2021
- Impfdatum
- 10.09.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Pruritus
Swelling
Symptomtext
arm swollen from elbow down to wrist(started 09/11/2021 and still present til present 09/16/2021). itching was present for couple of days (from 09/11/2021) but subsided. the swelling has gone down a bit; but from wrist to elbow on left arm swelling still present. pt advised to speak to pcp about any potential necessary treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- dm,htn
- Andere Medikamente
- non stated
- Allergien
- penicillin, rosuvastatin, vicodin, sulfametoxazole
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 16.09.2021
- Impfdatum
- 19.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Malaise
Pain
Symptomtext
achy, not feeling well for couple of days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 16.09.2021
- Impfdatum
- 16.08.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 19,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysstasia
Eating disorder
Gait inability
Pain
Psychomotor hyperactivity
Walking aid user
Symptomtext
a week after bot vaccines total body aches . went to er and doctor was given a walker wit seat . unable to stand or walk for long periods . ccould not tolerate solid foods , liquids only . Diagnosis hyperactive syndrome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- diabetic, depression
- Andere Medikamente
- dexalinent , Tylenol, diclofenac 75mg cyclobenfzaein ,Trazodone ,one a day vitamin multi vitamin sucralsate 1mg metformin , rybelsus , buprotion 150mg , nirtazapine 45mg risperidone ciclopirox ,
- Allergien
- shell fish ,lactose
- Vorherige Impfungen
- flu
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 11.09.2021
- Impfdatum
- 17.07.2021
- Beginn
- 17.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Contusion
Erythema
Hypokinesia
Joint stiffness
Limb discomfort
Peripheral swelling
Pruritus
Pyrexia
Skin mass
Vaccination complication
Symptomtext
problems with joints in elbows, knee and ankles they are horribly stiff; can barely move, can't move knees and arm; does not feel active as before; completely knocked off after 2nd dos; Right arm red to the touch; Right arm itches; 102.9 fever; Right arm bruised; Right arm has bumps all over; Right arm completely swollen; She can't work with her arm like this; This spontaneous case was reported by a nurse and describes the occurrence of CONTUSION (Right arm bruised), SKIN MASS (Right arm has bumps all over), PERIPHERAL SWELLING (Right arm completely swollen), LIMB DISCOMFORT (She can't work with her arm like this) and JOINT STIFFNESS (problems with joints in elbows, knee and ankles they are horribly stiff) in a 41-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was provided. On 17-Jul-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 2 dosage form. On 17-Jul-2021, the patient experienced CONTUSION (Right arm bruised), SKIN MASS (Right arm has bumps all over), PERIPHERAL SWELLING (Right arm completely swollen), LIMB DISCOMFORT (She can't work with her arm like this), ERYTHEMA (Right arm red to the touch), PRURITUS (Right arm itches) and PYREXIA (102.9 fever). On an unknown date, the patient experienced JOINT STIFFNESS (problems with joints in elbows, knee and ankles they are horribly stiff), HYPOKINESIA (can barely move, can't move knees and arm), ASTHENIA (does not feel active as before) and VACCINATION COMPLICATION (completely knocked off after 2nd dos). The patient was treated with IBUPROFEN (MOTRIN [IBUPROFEN]) at an unspecified dose and frequency; PARACETAMOL (TYLENOL) at an unspecified dose and frequency and DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at an unspecified dose and frequency. At the time of the report, CONTUSION (Right arm bruised), SKIN MASS (Right arm has bumps all over), PERIPHERAL SWELLING (Right arm completely swollen), LIMB DISCOMFORT (She can't work with her arm like this), JOINT STIFFNESS (problems with joints in elbows, knee and ankles they are horribly stiff), HYPOKINESIA (can barely move, can't move knees and arm), ASTHENIA (does not feel active as before), VACCINATION COMPLICATION (completely knocked off after 2nd dos), ERYTHEMA (Right arm red to the touch), PRURITUS (Right arm itches) and PYREXIA (102.9 fever) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medication was reported. Most recent FOLLOW-UP information incorporated above includes: On 26-Aug-2021: Significant follow-up : New event added
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 09.09.2021
- Impfdatum
- 02.07.2021
- Beginn
- 03.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Pain in extremity
Symptomtext
On 07/04/2021, 2 days after the vaccine, I had lightheadedness slight pain in my arm, it was very mild the 1st day or so. The site pain never amounted to anything at that point. My lightheaded lasted approximately for 2 weeks. It was very mild. I never had lightheadedness in my whole life. It was very insignificant and it disappeared. I did not have the lightheadedness in July when I received the 2nd dose of Moderna. I saw the doctor the day of the 1st shot. I had the shot at 09:00 AM at 11:30AM I saw PA. She took my BP- normal, checked my heart. All normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- high blood pressure, bad back and neck- scoliosis
- Andere Medikamente
- amlodipine, benazepril, atenolol, allergy tablets-Benadryl.
- Allergien
- Cipro -12/07/2017, nitrofurantoin 100 mg -07/30/2019
- Vorherige Impfungen
- polio shot/1954 or 1955/ in Brooklyn, immediately after the shot my arm was stiff. It wasn't long lasting. 7 years ago, pneumoni
- Staat
- MT
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 09.09.2021
- Impfdatum
- 02.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Eye pruritus
Glossodynia
Injection site erythema
Injection site irritation
Injection site pruritus
Injection site swelling
Lacrimation increased
Rash
Swollen tongue
Pruritus
Throat tightness
Urticaria
Symptomtext
Within 5 minutes of receiving the vaccine and being asked to wait by the pharmacy I began getting hives on my eyebrows, back of arms by my armpits, chest, jawline and neck. Within 10 minutes I had a full blown rash, hives, sore/swollen tongue, itchy/watery eyes and throat tightening. I was given 50mg of diphenhydramine and was monitored by a pharmacist for 50 minutes post vaccine. I was told to call 911 if chest pain/shortness of breath occurred. I monitored my symptoms on my own after 1hr of being monitored by the pharmacist. The allergic reaction continued for 48hrs. Chest tightness occurred 9-10hrs after injection but was reduced with another 50mg dose of diphenhydramine. The injection site became swollen, red, irritated and incredibly itchy 7 days after the injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Was referred to an allergist by my primary care physician and will have the 2nd dose administered by my PCP on 10/1 and monitored.
- Aktuelle Erkrankungen
- Cold (possible Delta variant; non confirmed) beginning 8/16 - 8/28. Symptoms included severe headache, sore throat, watery/itchy eyes, nasal congestion, runny nose, body ache, fever at highest 101.4?, cough, chest congestion, nausea, diarrhea.
- Vorgeschichte
- N/A
- Andere Medikamente
- Oral birth control tablet (once daily)
- Allergien
- Shellfish, tree nuts, Hydroxychloroquine, Sulfa drugs, contrast iodine, bees, cats, dogs, pollen, grass, noxious weeds, strawberries, hay, dairy & some egg products.
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 08.09.2021
- Impfdatum
- 05.08.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pain in extremity
Peripheral swelling
Symptomtext
Arm was sore and swollen first 2 days, then again one week later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Antibiotics
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 06.09.2021
- Impfdatum
- 21.07.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Urticaria
Symptomtext
within 12hrs of first dose (July 21,2021) I woke up with extremely itchy & red hive on th e back of my left thigh which is still present 6wks later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- allergic to bees, greens head flies, seafood
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 24.07.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 28,0
- Dosis
- 2
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Depressed mood
Eye haemorrhage
Feeling abnormal
Hyperhidrosis
Myalgia
Pain in extremity
Symptomtext
large broken blood vessel in his left eye on outer edge of the iris; He felt terrible/He felt emotionally terrible for 5 to 10 minutes; He felt depressed; His right arm was sore on that day after 2nd dose/He had body aches; chills on next day; At night, he sweated a lot.; His right arm was sore on that day after receiving 2nd dose; This spontaneous case was reported by a consumer and describes the occurrence of EYE HAEMORRHAGE (large broken blood vessel in his left eye on outer edge of the iris) in a 38-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 24-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 21-Aug-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced PAIN IN EXTREMITY (His right arm was sore on that day after receiving 2nd dose). On 22-Aug-2021, the patient experienced MYALGIA (His right arm was sore on that day after 2nd dose/He had body aches), CHILLS (chills on next day) and HYPERHIDROSIS (At night, he sweated a lot.). On 24-Aug-2021, the patient experienced FEELING ABNORMAL (He felt terrible/He felt emotionally terrible for 5 to 10 minutes) and DEPRESSED MOOD (He felt depressed). On 25-Aug-2021, the patient experienced EYE HAEMORRHAGE (large broken blood vessel in his left eye on outer edge of the iris) (seriousness criterion medically significant). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, EYE HAEMORRHAGE (large broken blood vessel in his left eye on outer edge of the iris), MYALGIA (His right arm was sore on that day after 2nd dose/He had body aches), CHILLS (chills on next day), HYPERHIDROSIS (At night, he sweated a lot.), FEELING ABNORMAL (He felt terrible/He felt emotionally terrible for 5 to 10 minutes), DEPRESSED MOOD (He felt depressed) and PAIN IN EXTREMITY (His right arm was sore on that day after receiving 2nd dose) outcome was unknown. Action taken with mRNA-1273 in response to the events was not applicable. No concomitant medication details were reported. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. Further information has been requested.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. Further information has been requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 14.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Body temperature
Contusion
Dizziness
Extra dose administered
Feeding disorder
Headache
Heart rate
Nausea
Pyrexia
Vaccination site bruising
Vaccination site erythema
Vaccination site pain
Vaccination site pruritus
Vaccination site swelling
Symptomtext
Extra dose administered; Started with bruise that now has become much larger; She is also feeling dizzy; She has headache; It is itchy.; On same day at night, she started with little fever; She had nausea.; Her left arm started hurting at injection site; Injection site is swollen; It is red; She had stomach cramps; She started with bruise that now has become much larger.; She hasn't been eating much.; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (She is also feeling dizzy), EXTRA DOSE ADMINISTERED (Extra dose administered), ABDOMINAL PAIN UPPER (She had stomach cramps), CONTUSION (She started with bruise that now has become much larger.) and FEEDING DISORDER (She hasn't been eating much.) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Atrial fibrillation. Concomitant products included FAMOTIDINE, LOSARTAN, METOPROLOL SUCCINATE (TOPROL), ERGOCALCIFEROL (VITAMIN D [ERGOCALCIFEROL]), EZETIMIBE (ZETIA), CELECOXIB (CELEBREX), KETAMINE and CLOPIDOGREL BISULFATE (PLAVIX) for an unknown indication. On 14-Aug-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 14-Aug-2021, the patient experienced ABDOMINAL PAIN UPPER (She had stomach cramps), CONTUSION (She started with bruise that now has become much larger.), FEEDING DISORDER (She hasn't been eating much.), VACCINATION SITE PRURITUS (It is itchy.), PYREXIA (On same day at night, she started with little fever), NAUSEA (She had nausea.), VACCINATION SITE PAIN (Her left arm started hurting at injection site), VACCINATION SITE SWELLING (Injection site is swollen) and VACCINATION SITE ERYTHEMA (It is red). On 16-Aug-2021, the patient experienced DIZZINESS (She is also feeling dizzy), VACCINATION SITE BRUISING (Started with bruise that now has become much larger) and HEADACHE (She has headache). On an unknown date, the patient experienced EXTRA DOSE ADMINISTERED (Extra dose administered). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency. At the time of the report, DIZZINESS (She is also feeling dizzy), ABDOMINAL PAIN UPPER (She had stomach cramps), CONTUSION (She started with bruise that now has become much larger.), FEEDING DISORDER (She hasn't been eating much.), VACCINATION SITE BRUISING (Started with bruise that now has become much larger), VACCINATION SITE PRURITUS (It is itchy.), PYREXIA (On same day at night, she started with little fever), NAUSEA (She had nausea.), VACCINATION SITE PAIN (Her left arm started hurting at injection site), VACCINATION SITE SWELLING (Injection site is swollen), VACCINATION SITE ERYTHEMA (It is red) and HEADACHE (She has headache) outcome was unknown and EXTRA DOSE ADMINISTERED (Extra dose administered) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 16-Aug-2021, Heart rate: increased (High) Increased. On an unknown date, Body temperature: 101 (High) 101.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: 101; Test Date: 20210816; Test Name: Heart rate; Result Unstructured Data: Increased
- Aktuelle Erkrankungen
- Atrial fibrillation
- Vorgeschichte
- -
- Andere Medikamente
- FAMOTIDINE; LOSARTAN; TOPROL; VITAMIN D [ERGOCALCIFEROL]; ZETIA; CELEBREX; KETAMINE; PLAVIX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 17.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Hives; This spontaneous case was reported by a pharmacist and describes the occurrence of URTICARIA (Hives) in an 18-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-Aug-2021, the patient experienced URTICARIA (Hives). At the time of the report, URTICARIA (Hives) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medication was not provided. Treatment information was not reported. Patient who received the Moderna vaccine 30 minute ago and now has hives, but not all over the body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 02.09.2021
- Impfdatum
- 16.07.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Pruritus
Vaccination site pain
Symptomtext
Intermittent itching palms,bilateral itching palms,intermittent itching knuckles; Pain at the injection site; Achy knee issue; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (Intermittent itching palms,bilateral itching palms,intermittent itching knuckles), VACCINATION SITE PAIN (Pain at the injection site) and ARTHRALGIA (Achy knee issue) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 16-Jul-2021, the patient experienced VACCINATION SITE PAIN (Pain at the injection site) and ARTHRALGIA (Achy knee issue). On 26-Jul-2021, the patient experienced PRURITUS (Intermittent itching palms,bilateral itching palms,intermittent itching knuckles). The patient was treated with PARACETAMOL (OTC VOLTAREN) for Adverse event, at an unspecified dose and frequency. On 20-Jul-2021, VACCINATION SITE PAIN (Pain at the injection site) had resolved. At the time of the report, PRURITUS (Intermittent itching palms,bilateral itching palms,intermittent itching knuckles) and ARTHRALGIA (Achy knee issue) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. The patient did not experience the same issues after receiving the second dose than compared to the first dose. Most recent FOLLOW-UP information incorporated above includes: On 17-Aug-2021: follow up contains added dose details and updated action taken of suspect vaccine and added event of aching in knees, updated outcome of itching both hands, treatment drug added
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 01.09.2021
- Impfdatum
- 22.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye swelling
Injection site erythema
Peripheral swelling
Rash
Rash erythematous
Rash pruritic
Swelling face
Symptomtext
Slight redness appeared on left arm 4 days after 2nd shot - June 25th. July 4th face swelled around eyes only. Went to ER on July 5th. Steroids were recommended but I opted out. Swelling was gone by July 15th. Rashes continued to spread & get worse covering both arms, upper thighs, torso & forehead. Left arm slightly swelled mid July but did not seek treatment; went away after about 2 weeks. Right arm swelled & left leg swelled on Aug 13th. Went to Urgent Care & was prescribed steroids - 20 mg once a day for 7 days. Arm swelling went down after the 7 days (Aug 20th) but leg swelling continued until Aug 24th. Rashes continued to spread to my lower back, down to my knees, back of my thighs, up from my torso across my chest. Right arm swelled again Aug 29th & legs & thighs swell again on Aug 30th. Rashes still continuing to itch & burn over 90% of body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- No tests.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Just the allergies as listed above
- Andere Medikamente
- Vitamin C
- Allergien
- Codeine, eggs, milk products, aspirin, alleve, tomatoes & products made with tomatoes,
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 01.09.2021
- Impfdatum
- 29.07.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Peripheral swelling
Pruritus
Symptomtext
arm swelling ,itching
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 30.08.2021
- Impfdatum
- 23.07.2021
- Beginn
- 24.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Respiratory tract congestion
Sinus disorder
Symptomtext
PATIENT STATED HE HAS BEEN EXPERIENCING SINUS ISSUES LIKE CONGESTION FOR 3 WEEKS POST INJECTION AND IS STILL HAVING RIGHT ARM ROTATOR CALF PAIN UNTIL NOW.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NOT KNOWN
- Vorgeschichte
- NOT KNOWN
- Andere Medikamente
- NOT KNOWN
- Allergien
- NO ALLERGIES
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 01.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Vaccination site mass
Symptomtext
a little rash; on my left arm, small bumps started to populate all over; This spontaneous case was reported by a consumer and describes the occurrence of RASH (a little rash) and VACCINATION SITE MASS (on my left arm, small bumps started to populate all over) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient experienced RASH (a little rash) and VACCINATION SITE MASS (on my left arm, small bumps started to populate all over). The patient was treated with ACETYLSALICYLIC ACID (ASPIRIN 81) on 11-Aug-2021 at an unspecified dose and frequency. At the time of the report, RASH (a little rash) and VACCINATION SITE MASS (on my left arm, small bumps started to populate all over) outcome was unknown. No concomitant drug information provided. Company Comment: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.. The company physician considers the reported events as non-serious, because there is no apparent rationale to deal them as serious. This case was linked to MOD-2021-289677 (Patient Link). Reporter did not allow further contact Most recent FOLLOW-UP information incorporated above includes: On 17-Aug-2021: Follow up received contain no new information.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.. The company physician considers the reported events as non-serious, because there is no apparent rationale to deal them as serious
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 15.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Product administered to patient of inappropriate age
Pyrexia
Symptomtext
Excessive sweating; Feeling feverish; Moderna Covid-19 vaccine administered to a 12 year old; This spontaneous case was reported by a consumer and describes the occurrence of HYPERHIDROSIS (Excessive sweating), PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (Moderna Covid-19 vaccine administered to a 12 year old) and PYREXIA (Feeling feverish) in a 12-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Jul-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (Moderna Covid-19 vaccine administered to a 12 year old). On 24-Jul-2021, the patient experienced HYPERHIDROSIS (Excessive sweating). 24-Jul-2021, the patient experienced PYREXIA (Feeling feverish). On 15-Jul-2021, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (Moderna Covid-19 vaccine administered to a 12 year old) had resolved. At the time of the report, HYPERHIDROSIS (Excessive sweating) and PYREXIA (Feeling feverish) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant drugs were provided No treatment drugs were provided. The patient said that she brought her son to the pharmacy and the Pharmacy Technician asked the Mother if her son who was 12 years of age would like the Pfizer or the Moderna Covid-19 vaccine.. The callers son received his first Moderna Covid-19 dose on 15-Jul-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 23.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Illness
Nausea
Product dose omission issue
Symptomtext
Sick; felt like having a fever, no actual fever.; more than 36 days from first vaccination; Nauseous; This spontaneous case was reported by a consumer and describes the occurrence of ILLNESS (Sick), FEELING ABNORMAL (felt like having a fever, no actual fever.), PRODUCT DOSE OMISSION ISSUE (more than 36 days from first vaccination) and NAUSEA (Nauseous) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. Concurrent medical conditions included Psoriasis. Concomitant products included METOPROLOL SUCCINATE for an unknown indication. On 23-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced ILLNESS (Sick), FEELING ABNORMAL (felt like having a fever, no actual fever.), PRODUCT DOSE OMISSION ISSUE (more than 36 days from first vaccination) and NAUSEA (Nauseous). At the time of the report, ILLNESS (Sick), FEELING ABNORMAL (felt like having a fever, no actual fever.) and NAUSEA (Nauseous) outcome was unknown and PRODUCT DOSE OMISSION ISSUE (more than 36 days from first vaccination) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient states she has BVC (no acronym provided) metoprolol succinate ER given for BVC. it was reported that patient was unable to get the second dose due to family issue. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 17-Aug-2021: Followup information received wherein new event was updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Psoriasis
- Vorgeschichte
- -
- Andere Medikamente
- METOPROLOL SUCCINATE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 22.06.2021
- Beginn
- 22.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Muscular weakness
Myalgia
Symptomtext
weakness in arm; Whole arm was affected,including shoulder and elbow soreness; This spontaneous case was reported by a consumer and describes the occurrence of MUSCULAR WEAKNESS (weakness in arm) and MYALGIA (Whole arm was affected,including shoulder and elbow soreness) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Jun-2021, the patient experienced MUSCULAR WEAKNESS (weakness in arm) and MYALGIA (Whole arm was affected,including shoulder and elbow soreness). The patient was treated with IBUPROFEN at a dose of 1 dosage form. At the time of the report, MUSCULAR WEAKNESS (weakness in arm) and MYALGIA (Whole arm was affected,including shoulder and elbow soreness) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No Concomitant products were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 24.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Fatigue
Hyperhidrosis
Lymphadenopathy
Myalgia
Nausea
Somnolence
Vomiting
Symptomtext
sleeping all day; sweating; redness; Vomiting; Nausea; her arm started getting sore / body aches.; swelling of lymph node; extremely tired; This spontaneous case was reported by a consumer and describes the occurrence of SOMNOLENCE (sleeping all day), HYPERHIDROSIS (sweating), ERYTHEMA (redness), VOMITING (Vomiting) and NAUSEA (Nausea) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 24-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced SOMNOLENCE (sleeping all day), HYPERHIDROSIS (sweating), ERYTHEMA (redness), VOMITING (Vomiting), NAUSEA (Nausea), MYALGIA (her arm started getting sore / body aches.), LYMPHADENOPATHY (swelling of lymph node) and FATIGUE (extremely tired). At the time of the report, SOMNOLENCE (sleeping all day), HYPERHIDROSIS (sweating), ERYTHEMA (redness), VOMITING (Vomiting), NAUSEA (Nausea), MYALGIA (her arm started getting sore / body aches.), LYMPHADENOPATHY (swelling of lymph node) and FATIGUE (extremely tired) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medication reported. Patient states that 6 hours later, arm started getting sore, redness, extremely tired, and the next day she slept all day. Patient also experienced body aches, swelling of the lymph node underneath the same arm of the injection, some nausea and vomiting and sweating. HCP told her should have received something like Tylenol or Ibuprofen for the pain, aches, soreness, and nausea and vomiting. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 01.07.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 31,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Gait disturbance
Musculoskeletal stiffness
Myalgia
Nodule
Pain
Pain in extremity
Peripheral swelling
Swelling face
Thrombophlebitis superficial
Papule
Tenderness
Symptomtext
had lumps on the back lower and front of her leg and right side of her face; superficial clotting in my superficial veins; muscular pain; right thigh was a bit tender; right thigh felt sore/The pain escalated to where my veins became very pronounced on my leg/The pain in her right leg has not gone away; it's still there; leg was stiff; The pain became more concentrated in the area and more intense; developed little bumps on the back of my right leg; hard to walk; This spontaneous case was reported by a consumer and describes the occurrence of TENDERNESS (right thigh was a bit tender), PAIN IN EXTREMITY (right thigh felt sore/The pain escalated to where my veins became very pronounced on my leg/The pain in her right leg has not gone away; it's still there), MUSCULOSKELETAL STIFFNESS (leg was stiff), PAIN (The pain became more concentrated in the area and more intense), PAPULE (developed little bumps on the back of my right leg), MYALGIA (muscular pain), NODULE (had lumps on the back lower and front of her leg and right side of her face), THROMBOPHLEBITIS SUPERFICIAL (superficial clotting in my superficial veins) and GAIT DISTURBANCE (hard to walk) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 05-Aug-2021, the patient experienced TENDERNESS (right thigh was a bit tender) (seriousness criteria disability and medically significant) and PAIN IN EXTREMITY (right thigh felt sore/The pain escalated to where my veins became very pronounced on my leg/The pain in her right leg has not gone away; it's still there) (seriousness criteria disability and medically significant). On 09-Aug-2021, the patient experienced MYALGIA (muscular pain) (seriousness criteria disability and medically significant). On 11-Aug-2021, the patient experienced THROMBOPHLEBITIS SUPERFICIAL (superficial clotting in my superficial veins) (seriousness criteria disability and medically significant). In August 2021, the patient experienced MUSCULOSKELETAL STIFFNESS (leg was stiff) (seriousness criteria disability and medically significant), PAIN (The pain became more concentrated in the area and more intense) (seriousness criteria disability and medically significant), PAPULE (developed little bumps on the back of my right leg) (seriousness criteria disability and medically significant) and GAIT DISTURBANCE (hard to walk) (seriousness criteria disability and medically significant). On an unknown date, the patient experienced NODULE (had lumps on the back lower and front of her leg and right side of her face) (seriousness criteria disability and medically significant). The patient was treated with ACETYLSALICYLIC ACID (ASPIRIN 81) on 11-Aug-2021 for Adverse event, at a dose of 81 mg once. At the time of the report, TENDERNESS (right thigh was a bit tender), PAIN IN EXTREMITY (right thigh felt sore/The pain escalated to where my veins became very pronounced on my leg/The pain in her right leg has not gone away; it's still there), MUSCULOSKELETAL STIFFNESS (leg was stiff), PAIN (The pain became more concentrated in the area and more intense), PAPULE (developed little bumps on the back of my right leg), MYALGIA (muscular pain), NODULE (had lumps on the back lower and front of her leg and right side of her face), THROMBOPHLEBITIS SUPERFICIAL (superficial clotting in my superficial veins) and GAIT DISTURBANCE (hard to walk) outcome was unknown. Concomitant medication not provided. Patient went to the hospital on 09Aug2021, where they diagnosed it as muscular pain. She went back to another better hospital on 11Aug2021, where she was diagnosed with superficial clotting in her superficial veins. The pain in her right leg has not gone away; it's still there now 17Aug2021. She went to a hematologist and neurologist, but they couldn't really help. Consent declined for safety to contact the patient's HCP. Pictures and documents provided were provided on 17 Aug 2021. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded This case was linked to MOD-2021-289664 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 17-Aug-2021: Non Significant Follow up appended for Document attachment. No changes in follow-up document.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 01.07.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 31,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Gait disturbance
Musculoskeletal stiffness
Myalgia
Nodule
Pain
Pain in extremity
Peripheral swelling
Swelling face
Thrombophlebitis superficial
Papule
Tenderness
Symptomtext
had lumps on the back lower and front of her leg and right side of her face; superficial clotting in my superficial veins; muscular pain; right thigh was a bit tender; right thigh felt sore/The pain escalated to where my veins became very pronounced on my leg/The pain in her right leg has not gone away; it's still there; leg was stiff; The pain became more concentrated in the area and more intense; developed little bumps on the back of my right leg; hard to walk; This spontaneous case was reported by a consumer and describes the occurrence of TENDERNESS (right thigh was a bit tender), PAIN IN EXTREMITY (right thigh felt sore/The pain escalated to where my veins became very pronounced on my leg/The pain in her right leg has not gone away; it's still there), MUSCULOSKELETAL STIFFNESS (leg was stiff), PAIN (The pain became more concentrated in the area and more intense), PAPULE (developed little bumps on the back of my right leg), MYALGIA (muscular pain), NODULE (had lumps on the back lower and front of her leg and right side of her face), THROMBOPHLEBITIS SUPERFICIAL (superficial clotting in my superficial veins) and GAIT DISTURBANCE (hard to walk) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 05-Aug-2021, the patient experienced TENDERNESS (right thigh was a bit tender) (seriousness criteria disability and medically significant) and PAIN IN EXTREMITY (right thigh felt sore/The pain escalated to where my veins became very pronounced on my leg/The pain in her right leg has not gone away; it's still there) (seriousness criteria disability and medically significant). On 09-Aug-2021, the patient experienced MYALGIA (muscular pain) (seriousness criteria disability and medically significant). On 11-Aug-2021, the patient experienced THROMBOPHLEBITIS SUPERFICIAL (superficial clotting in my superficial veins) (seriousness criteria disability and medically significant). In August 2021, the patient experienced MUSCULOSKELETAL STIFFNESS (leg was stiff) (seriousness criteria disability and medically significant), PAIN (The pain became more concentrated in the area and more intense) (seriousness criteria disability and medically significant), PAPULE (developed little bumps on the back of my right leg) (seriousness criteria disability and medically significant) and GAIT DISTURBANCE (hard to walk) (seriousness criteria disability and medically significant). On an unknown date, the patient experienced NODULE (had lumps on the back lower and front of her leg and right side of her face) (seriousness criteria disability and medically significant). The patient was treated with ACETYLSALICYLIC ACID (ASPIRIN 81) on 11-Aug-2021 for Adverse event, at a dose of 81 mg once. At the time of the report, TENDERNESS (right thigh was a bit tender), PAIN IN EXTREMITY (right thigh felt sore/The pain escalated to where my veins became very pronounced on my leg/The pain in her right leg has not gone away; it's still there), MUSCULOSKELETAL STIFFNESS (leg was stiff), PAIN (The pain became more concentrated in the area and more intense), PAPULE (developed little bumps on the back of my right leg), MYALGIA (muscular pain), NODULE (had lumps on the back lower and front of her leg and right side of her face), THROMBOPHLEBITIS SUPERFICIAL (superficial clotting in my superficial veins) and GAIT DISTURBANCE (hard to walk) outcome was unknown. Concomitant medication not provided. Patient went to the hospital on 09Aug2021, where they diagnosed it as muscular pain. She went back to another better hospital on 11Aug2021, where she was diagnosed with superficial clotting in her superficial veins. The pain in her right leg has not gone away; it's still there now 17Aug2021. She went to a hematologist and neurologist, but they couldn't really help. Consent declined for safety to contact the patient's HCP. Pictures and documents provided were provided on 17 Aug 2021. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded This case was linked to MOD-2021-289664 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 17-Aug-2021: Non Significant Follow up appended for Document attachment. No changes in follow-up document.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 27.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site swelling
Symptomtext
8/27/2021, Pt called to report bump at injection site for several days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 01.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 13,0
- Dosis
- 1
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Headache
Symptomtext
Having severe daily headaches, thought it was my migraines at first but now realize it?s different. Feels different. I feel that I?m even spacing out for lack of better description. Unsure what a doctor will do at this point other than tell me it my migraines or stress because I?m a women. In my experience women are dismissed when sharing their symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- You?re trying to blame my past medical history on this, but I feel like something has definitely changed within my body and mind. Mctd, hypothyroidism, migraine, adhd, asthma
- Andere Medikamente
- I didn?t take anything at the time/day of vaccination for fear of bad reaction.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 21.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Skin reaction
Skin warm
Symptomtext
Covid arm. Red large rash approximately 3 inches in diameter slightly warm to touch. Appeared in AM on 8th day after vaccination-length of duration unknown at this time as just presented
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma and allergies
- Andere Medikamente
- Allegra
- Allergien
- Antibiotic allergy to cefalexin and sensitivities to penicillin and sulfa drugs
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 20.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site swelling
Symptomtext
Swelling and redness at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 1 diabetes
- Andere Medikamente
- Prenatal, Humalog
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 18.08.2021
- Impfdatum
- 22.06.2021
- Beginn
- 29.06.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Burning sensation
Erythema
Heart rate
Heart rate increased
Lymphadenopathy
Peripheral swelling
Pruritus
Symptomtext
Swollen lymph node arm pit of the right arm. Very painful; Swollen lymph node arm pit of the right arm. Very painful; Right arm swelled; Burning sensation; Elevated resting heart rate of 105; itchy/ itchy around my neck; red rash; This spontaneous case was reported by a consumer and describes the occurrence of PERIPHERAL SWELLING (Right arm swelled), BURNING SENSATION (Burning sensation), HEART RATE INCREASED (Elevated resting heart rate of 105), PRURITUS (itchy/ itchy around my neck) and ERYTHEMA (red rash) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 040C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Non-smoking, non-drinking, physically active. History of allergies to penicillin, and Erythromycin. Allergies to 37 indoor and outdoor allergens. Previously administered products included for an unreported indication: BENADRYL ALLERGY [DIPHENHYDRAMINE HYDROCHLORIDE] until 30-Jul-2021. Concurrent medical conditions included Penicillin allergy, Allergy to antibiotic (Allergy to Erythromycin), Allergy to molds (Allergies to Homodendrum), Alternaria infection (Allergy to Alternaria), Allergy to molds (Allergy to Helminsthosporium), Allergy to molds (Allergy to Fusarium), Allergy to molds (Allergy to Stemphylium), Allergy to molds (Allergy to Curvularia), Allergy to molds (Allergic to Pullaria), Allergy to molds (Allergic to Aspergillus), Allergy to molds (Allergic to Epicoccum), Dust allergy (Allergic to Dust mites), Allergy to animals (Allergic to Dogs), Allergy to animals (Allergic to Cats), Allergy to feathers (Allergy to cockroaches), Allergy to insect sting, Grass allergy, Allergy to plants (Allergic to Sorrel plant), Ragweed allergy, Allergy to plants (Allergic to English Plantain), Allergy to plants (Allergic to Lamb's Quarters), Allergy to plants (Allergic to Pigweed), Allergy to plants (Allergic to Cockelbur weed plant), Nettle rash (Allergic to Nettle weed plant), Allergy to plants (Allergic to Palm Trees), Allergy to plants (Allergic to Melaleuca), Allergy to plants (Allergic to Australian pine), Allergy to plants (Allergic to White Pine), Allergy to plants (Allergic to Live Oak), Allergy to plants (Allergic to Red Cedar Elm), Allergy to plants (Allergic to Maple plant), Allergy to plants (Allergic to Ash Cottonwood) and Allergy to plants (Allergic to Brazilian Pepper tree). Concomitant products included BUDESONIDE (RHINOCORT [BUDESONIDE]) for an unknown indication. On 22-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 31-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 29-Jun-2021 at 6:20 AM, the patient experienced PERIPHERAL SWELLING (Right arm swelled), BURNING SENSATION (Burning sensation), HEART RATE INCREASED (Elevated resting heart rate of 105), PRURITUS (itchy/ itchy around my neck) and ERYTHEMA (red rash). On 30-Jun-2021 at 8:20 AM, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced AXILLARY PAIN (Swollen lymph node arm pit of the right arm. Very painful) and LYMPHADENOPATHY (Swollen lymph node arm pit of the right arm. Very painful). The patient was treated with IBUPROFEN, PSEUDOEPHEDRINE HYDROCHLORIDE (ADVIL FLU & BODY ACHE) at an unspecified dose and frequency. On 04-Jul-2021, AXILLARY PAIN (Swollen lymph node arm pit of the right arm. Very painful) and LYMPHADENOPATHY (Swollen lymph node arm pit of the right arm. Very painful) had resolved. At the time of the report, PERIPHERAL SWELLING (Right arm swelled), BURNING SENSATION (Burning sensation), HEART RATE INCREASED (Elevated resting heart rate of 105), PRURITUS (itchy/ itchy around my neck) and ERYTHEMA (red rash) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Heart rate: high (High) Heart rate running in low 100's. Patient treated the side effects with Benadryl ( Diphenhydramine Hydrochloride ) after taking the vaccine. The rash on the arm went away in few hours. Patient took Advil ( Ibuprofen ) for the lymph node discomfort and elevated Heart rate. Heart rate still continues to be elevate than normal until today. This case was linked to MOD-2021-272229 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 01-Aug-2021: Follow up report received on 01 Aug 2021, Added medical history, concomitant medications and events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- Test Name: Heart rate; Result Unstructured Data: Heart rate running in low 100's
- Aktuelle Erkrankungen
- Allergy to animals (Allergic to Dogs); Allergy to animals (Allergic to Cats); Allergy to antibiotic (Allergy to Erythromycin); Allergy to feathers (Allergy to cockroaches); Allergy to insect sting; Allergy to molds (Allergy to Stemphylium); Allergy to molds (Allergy to Helminsthosporium); Allergy to molds (Allergy to Fusarium); Allergy to molds (Allergy to Curvularia); Allergy to molds (Allergies to Homodendrum); Allergy to molds (Allergic to Pullaria); Allergy to molds (Allergic to Epicoccum); Allergy to molds (Allergic to Aspergillus); Allergy to plants (Allergic to White Pine); Allergy to plants (Allergic to Sorrel plant); Allergy to plants (Allergic to Red Cedar Elm); Allergy to plants (Allergic to Pigweed); Allergy to plants (Allergic to Palm Trees); Allergy to plants (Allergic to Melaleuca); Allergy to plants (Allergic to Maple plant); Allergy to plants (Allergic to Live Oak); Allergy to plants (Allergic to Lamb's Quarters); Allergy to plants (Allergic to English Plantain); Allergy to plants (Allergic to Cockelbur weed plant); Allergy to plants (Allergic to Brazilian Pepper tree); Allergy to plants (Allergic to Australian pine); Allergy to plants (Allergic to Ash Cottonwood); Alternaria infection (Allergy to Alternaria); Dust allergy (Allergic to Dust mites); Grass allergy; Nettle rash (Allergic to Nettle weed plant); Penicillin allergy; Ragweed allergy
- Vorgeschichte
- Comments: Non-smoking, non-drinking, physically active. History of allergies to penicillin, and Erythromycin. Allergies to 37 indoor and outdoor allergens.
- Andere Medikamente
- RHINOCORT [BUDESONIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 14.08.2021
- Impfdatum
- 02.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Fatigue
Injection site erythema
Injection site rash
Myalgia
Symptomtext
Red, hard rash around injection site, muscular pain left arm, diarrhea, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoarthritis, DDD
- Andere Medikamente
- Vitafusion Vitamin D gummy Vitafusion womens multi vitamin gummy Natures bounty milk thistle Natures bounty cinnamon
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 09.08.2021
- Impfdatum
- 22.06.2021
- Beginn
- 30.06.2021
- Tage bis Beginn
- 8,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Head discomfort
Headache
Memory impairment
Neck pain
Pain
Symptomtext
Head feels heavy inside and have brain fog, forgetful, headaches atleast 4 times a week and causes base of head to hurt and neck- achy feeling. I take Aleve daily for this
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- MI in 2015
- Andere Medikamente
- Plavix, Rapatha, baby aspirin, multi vitamin, Vit D3 2000iu, super B complex
- Allergien
- Nome
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 09.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Urticaria
Symptomtext
Patient says the vaccine was administered in the middle of the upper arm (too low). Received vaccine ~2pm, by same day had redness, by next day a raised welt (goose egg). Pt happened to have MD appointment. MD concerned but didn't have pt take any meds. Pt had been icing, and continued icing. Resolved after 2-3 weeks. (NO MD visit as a direct result of adverse event, pt already had one scheduled and brought up incident at that appt)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 08.08.2021
- Impfdatum
- 21.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Symptomtext
Moderna COVID-19 Vaccine EUA Fatigue for 3 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 05.08.2021
- Impfdatum
- 28.07.2021
- Beginn
- 28.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Skin warm
Symptomtext
Massive red patch appeared hours after injection and has gotten larger and larger since. It is painful to the touch and red hot. It had been a week since I had the shot so I called the clinic today to ask about it and the on call pharmacist told me to report it and schedule a doctor's appointment for tomorrow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Going to the doctor asap.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma PCOS
- Andere Medikamente
- Nortrel birth control Zyrtec allergy medicine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 04.08.2021
- Impfdatum
- 01.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Limb discomfort
Nodule
Pain in extremity
Peripheral swelling
Symptomtext
Big knot and swelling under left arm, painful, really uncomfortable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 03.08.2021
- Impfdatum
- 23.07.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysphagia
Oropharyngeal pain
Pharyngeal swelling
Rash
Urticaria
Symptomtext
Sore throat evolved into swelling of the throat and difficulty swallowing, next day hives developed under both arms and arm pit areas as well as some on hands and feet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None other than Hypertension
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Losartin, Atorvastatin, Clopidogrel, Amlopipine, Carvedilol,
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 02.08.2021
- Impfdatum
- 24.07.2021
- Beginn
- 25.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Impaired driving ability
Motion sickness
Nausea
Pain in extremity
Symptomtext
Was having really bad nausea, no other symptoms besides arm pain. Nausea decreased, by the 3rd day, July 27th, I was only a little nauseous and especially when looking at screens. Since then, I still have a small amount of lingering nausea. I can still function my daily activities, but I can?t looks at screens for too long, drive for too long, or if I?m not driving I get car sick really easily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Bupropion and Birth Control
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 01.08.2021
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
patient felt very dizzy for more than an hour
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NOT KNOWN
- Vorgeschichte
- NOT KNOWN
- Andere Medikamente
- NOT SURE
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 31.07.2021
- Impfdatum
- 13.05.2021
- Beginn
- 17.06.2021
- Tage bis Beginn
- 35,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dyskinesia
Loss of personal independence in daily activities
Muscle spasms
Pain
Symptomtext
after receiving the second shot on June 17th I experienced significant debilitating pain all throughout my body that lasted for 12+ hours. a muscle on the left side of my back has been in constant spasm ever since. the intensity varies from minor annoyance to debilitating pain that interrupts whatever I may be doing. icing doesn't seem to help. I started taking magnesium a few days ago, too soon to tell if it's helping. yesterday my right thumb started spasming without pain and was moving outside of my control. it subsided after a few hours and has not repeated. today the muscles around the left side of my mouth have been spasming. as noted above, back spasms persist daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- lyme
- Andere Medikamente
- none
- Allergien
- advil, apricots
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 28.07.2021
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Dizziness
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Additional Details: patient indicated slight dizziness post vaccination, questioned pateint on feeling nervous, patient indicted that he felt slighly anxious and did not eat all day, gave patient Gatorade, and had him lay down. Patinetts dizzinies resolved after few minutes, and drinking Gatorade. Asked patient if he wanted an ambulance, he indicated that he was feeling normal and did not want an ambulance. Follow up call with patient at end of my shift, patinet indicated that he had a meal and felt perfectly fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 26.07.2021
- Impfdatum
- 15.07.2021
- Beginn
- 17.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Patient states she has bumpy rash on arms, legs, stomach, and back. She states it is not itchy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- multiple back surgeries
- Andere Medikamente
- amitriptyline 25mg, levocetirizine 5mg, clonazepam 0.5mg, meloxicam 15mg, acetaminophen 500mg
- Allergien
- gabapentin, allegra, nsaids
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 26.07.2021
- Impfdatum
- 22.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Arthralgia
Asthenia
Back pain
Decreased appetite
Disturbance in attention
Fatigue
Feeling abnormal
Headache
Pain
Photophobia
Sleep disorder
Symptomtext
Approx 17hrs after receiving shot I started feeling a mild headache and trouble concentrating. I felt physically weaker and mild stomach ache with my eyes sensitive to light. The following morning I felt almost back to normal. The following evening 2 days after receiving shot I felt a lot of Upper back and shoulder pain. I felt like throwing up but did not. I only slept 3 hours that night and was physically soar. I ate only a can of chicken noodle soup and drank a can of ginger ale Sunday 7/25/21. I slept well last night but still feel tired and a little brain fog. I ate a good breakfast this AM and believe now three days after my second shot I will likely be almost back to normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- None so far
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 26.07.2021
- Impfdatum
- 24.07.2021
- Beginn
- 26.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Polymenorrhoea
Symptomtext
My period came early. (The last date of my menstral cycle is 7/6/2021) When I woke up this morning my menstral cycle has begun again. I also want to add on 7/24/21 I had such strong body aches that night I became rehabilitated from that night until this morning. Aches are gone but my period has now started again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 23.07.2021
- Impfdatum
- 30.06.2021
- Beginn
- 30.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Feeling abnormal
Hypersensitivity
Lip swelling
Pain
Pain in extremity
Peripheral swelling
Pyrexia
Skin warm
Swelling face
Swollen tongue
Symptomtext
severe allergic reaction. arm swelled up immediatly following shot then after 30 minutes my face lips & tongue swelled up bad and I felt very weak, I had a fever and my arm was very hot hurting and swollen for many days. I still do ot feel back to my normal self. I had to take prednisone as well as benadryl for over a week. use ice packs on my arm which hurt me very much to use..
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- NCS=neurocardiogenic syncope, MCAS=mast cell activation syndrome, Chiari 1, hypertension/hypotension, elevated cholesterol now under control.
- Andere Medikamente
- lisinopril, rosuvastatin, lovaza
- Allergien
- codeine, sulfa, augmentin, levaquin, motrin, tetracyclin, contrast dye, midodrine
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 22.07.2021
- Impfdatum
- 13.06.2021
- Beginn
- 13.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Dizziness
Fatigue
Headache
Myalgia
Nausea
Pain in extremity
Vomiting
Symptomtext
Arm pain; Fatigue; Muscle ache; Leg pain; Dizziness; Headache; Nausea; Vomiting; Diarrhea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Iodine
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.07.2021
- Impfdatum
- 13.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
PT DEVELOPED HIVED 2 DAYS AFTER 2ND SHOT... WENT TO DR AND THE HIVES HAVE WENT AWAY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 22.07.2021
- Impfdatum
- 07.07.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Erythema
Headache
Herpes zoster
Inflammation
Pain
Rash erythematous
Skin warm
Vertigo
Symptomtext
1. Day after injection, I had local reaction to upper arm of redness, inflammation and warmth to skin in more than 1 spot. No treatment 2. The day after the injection, I woke up with a headache and vertigo. Took Ibuprofen for headache, no other treatment 3. 6 days later I noticed red bumps that then over the next few days turned into blisters. I was experiencing a right sided headache and sharp, shooting pains. On Saturday, 7/ 17/2021, I went and was diagnosed with shingles. I was prescribed Valacyclovir 1gm TID for 7 days. ( however, nothing was given for pain or inflammation. On Monday, 07/19/21 I went to my pcp who again confirmed Shingles, and prescribed Gabapentin 300mg BID for pain and Prednisone (tapered dose) for inflammation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- See above.
- Aktuelle Erkrankungen
- Fibromyalgia, osteoarthritis, Hypertension
- Vorgeschichte
- Fibromyalgia, osteoarthritis
- Andere Medikamente
- Tramadol , Losartan, Vitamin D, probiotic
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 20.07.2021
- Impfdatum
- 19.07.2021
- Beginn
- 19.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Symptomtext
Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 18.07.2021
- Impfdatum
- 07.07.2021
- Beginn
- 17.07.2021
- Tage bis Beginn
- 10,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Chills
Headache
Injection site pain
Muscle spasms
Nausea
Pain
Pain in extremity
Pyrexia
Symptomtext
2nd vaccination on 7/6/2021@7pm On 7/7/2021 at 10am I began to feel achy, fevered and nauseous. By 12:00pm I was completely incapacitated with pain throughout my body, back and joints and injection sight arm. Extreme headache and both chills and fevered with vomiting . These symptoms subsided 8-10hrs later and had no symptoms the following morning 7/8/2021 and resumed normal work and activities. On 7/17/2021 @8:00am I felt some muscle spasms and pain in my left arm (injection site) by 10:00am I was completely incapacitated again with all of the listed symptoms above lasting through 11:00pm at which time they began to subside somewhat. Today 7/18/2021 I woke up to chills/fever, lower back pain, headache and general body aches and soreness. This continues at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 16.07.2021
- Impfdatum
- 13.07.2021
- Beginn
- 14.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Injection site erythema
Injection site urticaria
Mass
Pain
Pain in extremity
Pruritus
Skin warm
Symptomtext
The following day I had a round, itchy, painful, red lump. It is hot to the touch. Very painful if arm rubs against something. But today, 3 days later, it seems to be spreading. At least 5 inches uneven n 5 inches across but going to back of arm. It feels like a big lump that's very hot to touch. There are also white marks in red area like hives?
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 16.07.2021
- Impfdatum
- 15.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Feeling cold
Symptomtext
COLD FEELING AND DIZZY, BLOOD PRESSURE 198/95 PULSE 119 NO RASH, SWELLING OR DIFFICULTY I N BREATHING. PARAMEDICS CAME AND TOOK HER TO HOSPITAL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- BLOOD PRESSURE 198/95 PULSE 119
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 16.07.2021
- Impfdatum
- 05.07.2021
- Beginn
- 14.07.2021
- Tage bis Beginn
- 9,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Herpes zoster
Pain
Symptomtext
The patient called to see if a prescription had been called in. Upon finding out nothing had been called in yet, I asked if the doctors office was going to call something in that day, and she said "yes, to take care of the shingles I got after the moderna shot you gave me." I inquired when the shingles appeared and she told me it was 1 day after the shot. She denied any problems with the first moderna shot. She said the blisters were on the right side of her torso and migrating to the right side of her back. She stated that Tylenol was helping with the pain. An rx for Valtrex came in later that day for her.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 16.07.2021
- Impfdatum
- 14.07.2021
- Beginn
- 14.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Feeling hot
Flushing
Oropharyngeal pain
Symptomtext
PATIENT FELT WARM AND WAS FLUSH-MENTIONED PAIN BEGINNING IN THROAT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- ASTHMA
- Andere Medikamente
- ASPIRIN-DIPYRIDAM, METFORMIN, BUSPIRONE, CITALOPRAM, CLONAZEPAM, HYDROXYZINE, VYVANSE ALBUTEROL
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 16.07.2021
- Impfdatum
- 03.07.2021
- Beginn
- 03.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain
Swelling
Symptomtext
Swollen, red, painful for 2weeks +
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Bronchitis
- Andere Medikamente
- None
- Allergien
- Ampicillin
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 15.07.2021
- Impfdatum
- 15.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cold sweat
Dizziness
Nausea
Pallor
Tinnitus
Symptomtext
PT'S FACE LOSE COLOAR . HE WAS VERY WHITE. HE ALSO HAD COLD SWEAT. HE FELT DIZZY AND HAD RINGING IN HIS EARS HE FELT LIKE HE WANTED TO THROW UP. HIS AUNT WANTED US TO CALL AMULANCE. THE PARAMEDIC CAME . ALL THE VITALS WERE NORMAL. HIS FACE COLOR STARTED COMING BACK. PARAMEDIC ALSO CHECKED IF THERE WERE RASHES ON HIS CHEST AND ARMS. NOTHING. PARA MEDIC ASKED PT WHETHER HE WANTED TO GO HOSPITAL, HE DECLINED. HE SAT 10 MORE MINUTES FOR OBSERVATION AND HE FELT WELL ENOUGH AND LEFT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 15.07.2021
- Impfdatum
- 06.07.2021
- Beginn
- 12.07.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Musculoskeletal stiffness
Peripheral swelling
Skin warm
Urticaria
Symptomtext
6 days post injection developed a welt on arm, but not at int site, Large Lymph node swelling on collarbone and stiff neck. 7 -14 additional welts on injection arm. Temperature on the arm is 96 on arm with swelling and 90 on non injection arm. Taking OTC benedryl and using OTC hydrocortisone on the 2 welts on int arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- No lines
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Keflex/Cipro
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 15.07.2021
- Impfdatum
- 15.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Nausea
Neck pain
Vision blurred
Symptomtext
Patient got nauseated, blurred vision, sore neck, chills that would not go away. 911 called and ambulance transported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 15.07.2021
- Impfdatum
- 01.06.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 31,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Malaise
Nasopharyngitis
Oropharyngeal pain
Pyrexia
Respiratory symptom
Rhinorrhoea
Symptomtext
On the second day after getting the second dose, I started having chills, general malaise like a cold, this increased to an internal fever, a lot of nasal mucus, sore throat, and now in the chest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arterial Hypertension
- Andere Medikamente
- Losartan potassium 100 mg Amlodipine 10 mg Furosamide 40 mg Acetaminophen 500 mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 14.07.2021
- Impfdatum
- 30.06.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 13,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site rash
Symptomtext
COVID arm - large, red circle around vaccine area. Itchy and rash like.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Ceclor
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 13.07.2021
- Impfdatum
- 06.07.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site erythema
Injection site pruritus
Injection site reaction
Injection site swelling
Injection site warmth
Skin texture abnormal
Symptomtext
Red, swelling, itching, warm to touch, raised and textured injection site seven days after injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Bipolar, skin cancer from moles, past recreational drug and persctiption abuse with over ten years off them, Marijuana use daily, former cigarette smoker.
- Andere Medikamente
- Tylenol 500mg, Naprosyn off and on, multi vitamin gummy, vitamin C gummy.
- Allergien
- Latex and natural rubber products, grass, lilacs, cypress, malt.
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 13.07.2021
- Impfdatum
- 30.06.2021
- Beginn
- 05.07.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pruritus
Injection site rash
Pain in extremity
Pyrexia
Skin warm
Symptomtext
Rash/itchy at injection site. Arm is warm and sore. Fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 12.07.2021
- Impfdatum
- 09.07.2021
- Beginn
- 11.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Rash
Rash erythematous
Skin discolouration
Symptomtext
Patient said that she breakout in black and red dots on both arms. She also has a headache along with the rash.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma
- Andere Medikamente
- albuterol inhaler, valtrex, flovent inhaler
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 12.07.2021
- Impfdatum
- 08.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphthous ulcer
Pyrexia
Symptomtext
Patient reported a high fever (104 degrees F) followed by Aphthous ulcers (canker sores) all over her mouth. She saw a dentist on 7/12/21 and will be seeing her PCP on 7/15/21. She said that she is treating the canker sores with salt water rinses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 10.07.2021
- Impfdatum
- 10.07.2021
- Beginn
- 10.07.2021
- 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
patient experienced dizziness and light headed as well as sweating. patient was seated. blood pressure checked and monitored. breathing and heart rate were normal. resolved within 10 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 09.07.2021
- Impfdatum
- 09.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Symptomtext
Patient developed itching on arms and one hive on her right arm approximately 5 minutes after dose. She stayed at site for approximately one hour. Her head and back started feeling itchy as well but she remained stable, given Benadryl by mouth. Patient was driven to urgent care locally and given Benadryl IM, prednisone and Zofran. No shortness of breath. Released with a Medrol dose pack.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Asthma, anxiety, depression, bipolar disorder
- Andere Medikamente
- Albuterol INhaler, D-Manos otc
- Allergien
- INfluenza vaccine- swollen arm and shortness of breath 3 to 4 days after, Tramaol, Percocet and ketorolac
- Vorherige Impfungen
- influenza vaccine-had swelling and shortness of breath 3 to 4 days after receiving the shot, was adult age in her 30's approxima
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 09.07.2021
- Impfdatum
- 30.06.2021
- Beginn
- 03.07.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Soars that looks like big mosquito bites located on the upper part of hands, elbows, knees and legs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Tylenol Centrum Allergy tablets
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 08.07.2021
- Impfdatum
- 25.06.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pruritus
Rash
Symptomtext
Sore ,pain after 2 hours later of the injection. in about one week, my upper arm started to get itchy and has some rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- no
- Andere Medikamente
- I got my Moderna Covid Vaccine on 06/25/2021. after two hours my arm where I got injection started sore and pain, it lasts about 2 days and pain has gone. and I notice my upper arm started itchy and I scratched, it had a big bump after s
- Allergien
- unkown
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 06.07.2021
- Impfdatum
- 02.07.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear discomfort
Ear pain
Headache
Sleep disorder
Symptomtext
Middle left ear blockage since July 2, 7pm Severe pain in left ear since July 2 Severe headache Pain was severe enough to disrupt sleep. There is some relief for a few hours whenever she takes advil. I went to a CVS Pharmacist on July 4th and she recommended melatonin to help her sleep As of the time of this report, the ear blockage comes and goes, the ear pain and accompanying headache was still severe. She has taken Advil to ease the pain so she can sleep
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Slight cold
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 05.07.2021
- Impfdatum
- 03.07.2021
- Beginn
- 05.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Inappropriate schedule of product administration
Nausea
Symptomtext
Patient reported headache and nausea. Both have gone away. This is being reported because patient received second dose of Moderna COVID Vaccine 14 days after first dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 05.07.2021
- Impfdatum
- 02.07.2021
- Beginn
- 04.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Symptomtext
Rash over shoulders and chest area. Strange red rash on instep of right foot about 3-4 inches in diameter. Showed up 36 hours after vaccine. Not too bothersome. appears to be more rash today 3 days later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None - tried hydrocortisone cream and using an allergy medicine. If continues to worsen will contact provider. No DIB.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- hypertension
- Andere Medikamente
- lisinopril
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 03.07.2021
- Impfdatum
- 22.06.2021
- Beginn
- 24.06.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pain in extremity
Symptomtext
right foot and ankle pain; stabbing pain on right knee.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 02.07.2021
- Impfdatum
- 02.07.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Fall
Symptomtext
Patient was administered the vaccine at approximately 10:25 am and advised that he should remain in the store for 15 minutes to monitor for possible adverse reactions. At approximately 10:30 am the patient walked out the front door of the store and immediately fell face first on the side walk. I was contacted and did an assessment. His blood pressure was 110/50 with a pulse of 50. He was fully oriented and stated he continued to feel light headed. An ambulance was called and the patient was taken to the hospital for evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None done at this facility. Unknown what was done at hospital
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- None reported
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 01.07.2021
- Impfdatum
- 21.06.2021
- Beginn
- 21.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abortion spontaneous
Chills
Exposure during pregnancy
Pyrexia
Symptomtext
Patient reports fever and chills at about 7pm after receiving her covid shot. She treated fever with Tylenol. She went to the doctor the following day and found out that she lost her baby. She was 5 weeks pregnant at the time of vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 30.06.2021
- Impfdatum
- 30.06.2021
- Beginn
- 30.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blindness
Dizziness
Nausea
Symptomtext
The patient said he is feeling nauseous and he said he cannot see after some seconds and also felt dizzy. we called 911 meanwhile the patient said after 5-10 minutes he can see and he still feel nauseous. He didn't go to the hospital with the paramedics. After paramedics left he said he felt fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- ASTHMA
- Vorgeschichte
- ASTHMA
- Andere Medikamente
- -
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 30.06.2021
- Impfdatum
- 19.06.2021
- Beginn
- 19.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Nausea
Vaccination site reaction
Symptomtext
she was admitted to hospital due to big reaction after getting the first shot; nausea; the dizziness hit her/ woke up at 8pm and dizziness was still there and kept on going; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE REACTION (she was admitted to hospital due to big reaction after getting the first shot) in a 47-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Epilepsy and Vertigo (Get really dizzy.). Concomitant products included LAMOTRIGINE (LAMICTAL), LEVETIRACETAM (KEPPRA [LEVETIRACETAM]) and CARBAMAZEPINE (TEGRETOL) for an unknown indication. On 19-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 19-Jun-2021, the patient experienced VACCINATION SITE REACTION (she was admitted to hospital due to big reaction after getting the first shot) (seriousness criterion hospitalization) and DIZZINESS (the dizziness hit her/ woke up at 8pm and dizziness was still there and kept on going). On an unknown date, the patient experienced NAUSEA (nausea). The patient was hospitalized on 19-Jun-2021 due to VACCINATION SITE REACTION. At the time of the report, VACCINATION SITE REACTION (she was admitted to hospital due to big reaction after getting the first shot), DIZZINESS (the dizziness hit her/ woke up at 8pm and dizziness was still there and kept on going) and NAUSEA (nausea) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. On 20-Jun-2021 patient went to the hospital and had blood work done but no results were reported. Treatment reported is unknown nausea medication. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Epilepsy; Vertigo (Get really dizzy.)
- Andere Medikamente
- LAMICTAL; KEPPRA [LEVETIRACETAM]; TEGRETOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 30.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diabetes mellitus inadequate control
Pain in extremity
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of DIABETES MELLITUS INADEQUATE CONTROL (blood sugar is skyscraping since the shot) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Diabetes. Concomitant products included INSULIN for an unknown indication. On 18-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 18-Jun-2021, the patient experienced DIABETES MELLITUS INADEQUATE CONTROL (blood sugar is skyscraping since the shot) (seriousness criterion medically significant) and PAIN IN EXTREMITY (Arms is a little sore). At the time of the report, DIABETES MELLITUS INADEQUATE CONTROL (blood sugar is skyscraping since the shot) and PAIN IN EXTREMITY (Arms is a little sore) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No Treatment information was reported. It was reported that patient is with insulin pump but is not helping. This case concerns a 59-year-old male with a serious unexpected event of diabetes mellitus inadequate control, and non-serious pain in extremity. Event latency 1 day after first dose mRNA-1273. Based on current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.; Sender's Comments: This case concerns a 59-year-old male with a serious unexpected event of diabetes mellitus inadequate control, and non-serious pain in extremity. Event latency 1 day after first dose mRNA-1273. Based on current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Diabetes
- Vorgeschichte
- -
- Andere Medikamente
- INSULIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 29.06.2021
- Impfdatum
- 26.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Dizziness
Fall
Tachyphrenia
Symptomtext
After receiving the Moderna vaccine, the patient was sitting in a chair in the pharmacy waiting area. About 5 minutes afterwards, he fell out of his chair. Upon asking the patient if he was okay and what happened, he reported he felt dizzy with racing thoughts on his mind. Then he lost his balance, slipped out of his chair, and fell to the floor. He stated he has dizziness after every vaccine he has received in the past. He sat back in the chair and rested, and also reported he felt better. The supervisor on duty provided the patient with water. About 15 minutes after falling, the patient stated he felt fine and wanted to leave. He was stable upon standing up from the chair. I informed him if he experiences any other symptoms, that he should call my pharmacy, or if he experiences anaphylaxis, he should call 911 and seek immediate medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Supervisor on duty asked the patient if he would like to be taken to the hospital emergency department, but patient stated he did not need to go and said he felt fine.
- Aktuelle Erkrankungen
- Patient denies having other illnesses at the time of vaccination and up to one month prior.
- Vorgeschichte
- Patient denies having any chronic or long-standing health conditions.
- Andere Medikamente
- Patient denies taking prescription, over-the-counter medications, dietary supplements, or herbal remedies at the time of vaccination.
- Allergien
- Patient reports to have no known allergies to food, medication, or other products.
- Vorherige Impfungen
- dizziness after receiving any vaccine throughout his whole life
- Staat
- AL
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 28.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 19.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear pain
Facial pain
Herpes zoster
Symptomtext
shingles -outbreak on left side face, in mouth, sinus. Also face and ear pain. Ongoing treatment is antiviral meds and antibiotics. I have been under the care of my General Physician and ophthalmologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Pseudotumor cerebri, asthma, hypothyroid
- Andere Medikamente
- Levothyroxine, topimax, musinex, Zyrtec, asmanex, vitamin d, vitamin b12, vitamin c, Xopenex
- Allergien
- Sulfa, penicillin, keflex
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 28.06.2021
- Impfdatum
- 19.06.2021
- Beginn
- 27.06.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoaesthesia
Injection site erythema
Injection site pruritus
Pyrexia
Symptomtext
Pt has had on/off fevers since the date of vaccination on 6/19/21. These have responded to acetaminophen use. However, today she reports that beginning yesterday 6/27/21 she has started to see more redness around the injection site. She states her range of motion is ok, but in addition to the redness she as a little bit of itchiness and a little bit of numbness in that arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 28.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain in extremity
Peripheral swelling
Symptomtext
Small reddish circle, swollen sore arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Bronchitis, Multiple Sclerosis, Hyperthyroidism.
- Andere Medikamente
- Aubagio 14mg, Topiramate 50mg, Levothyroxine 25mcg, Omeprazole Dr 20mg, Amlodipine Besylate 5mg, Lisinopril 5mg, Trazodone Hcl 1 tablet at bedtime, Rosuvastatin Calcium 20mg, Meloxican 15mg, Tramadol Hc 50mg, Dicyclomine 10mg, Eb-N5 (medica
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 28.06.2021
- Impfdatum
- 22.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema of eyelid
Ocular hyperaemia
Pain in extremity
Symptomtext
painful arm for 1 to 2 days and after 3 days paitent both eyes were red (blood shot) and and the left eye has redness and bottom of eyelid is brown to red spot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- -
- Andere Medikamente
- no
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 28.06.2021
- Impfdatum
- 04.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 24,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature decreased
Chills
Pyrexia
Vomiting
Symptomtext
Chills, shivering, low temperature (95? F), vomiting followed by fever (101? F)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 27.06.2021
- Impfdatum
- 22.06.2021
- Beginn
- 22.06.2021
- 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
Erythema
Fatigue
Headache
Injection site warmth
Pain
Pyrexia
Symptomtext
Patient ran fever of up to 102, reports headache, fatigue, body aches, lack of appetite, redness, heat at site of injection. Patient used only Tylenol to treat. Patient states that 5 days later she is finally feeling a little better
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 26.06.2021
- Impfdatum
- 11.06.2021
- Beginn
- 11.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Rash macular
Symptomtext
Large red patch area (3 inches in diameter)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash macular
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 26.06.2021
- Impfdatum
- 19.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Pain in extremity
Symptomtext
I had a sore arm for a few days following the injection, which was to be expected. Today, however, exactly one week post injection, I noticed some itching at the injection site. Upon visualization, there is an area of localized small raised and reddened areas at the injection site. There is also warmth present at the site of injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Sinus cold two weeks prior
- Vorgeschichte
- no
- Andere Medikamente
- Spironolactone 100mg once a day, prenatal, Claritin, krill oil
- Allergien
- No Known food or drug allergies
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 26.06.2021
- Impfdatum
- 20.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pruritus
Injection site warmth
Skin reaction
Symptomtext
appears to be a delayed localized cutaneous reaction developing 6 days post vaccination, that spans about 6-8 inches in diameter and is hot and itchy. referred to Md
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- ??
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 26.06.2021
- Impfdatum
- 26.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fatigue
Nausea
Pallor
Sensation of foreign body
Symptomtext
Felt nausea, dizziness, Felt something in throat, after couple of minutes, At mention of throat 911 was called, EMS arrived less than 5 minutes, observed, took blood pressure, checked pulse, blood oxygen checked. Ems said he looked pale, continued to observe patient for about 30minutes, Mention of patient possibly experiencing panic attack, had history of in past. He was feeling fine by then, no need to go to hospital. Police followed him home. I called patient at 3:33PM he was home, said throat was fine, he just felt tired, He said he was o k .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Has upcoming appointment with a physician for possible heart valve issue .
- Andere Medikamente
- unknown
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 26.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site reaction
Rash pruritic
Skin exfoliation
Swelling
Symptomtext
About a week after the first dose of COVID-19 Moderna vaccine, I developed an itchy rash around the area where I was injected (left arm). I took an antihistamine allergy pill (50mg) to help with the swelling. It's still red, flakey, and oddly shaped currently (06/26/2021). Symptom is mild thus far, but I wanted to note it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A -- symptoms are mild thus far, so I don't think a medical test is necessary.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 26.06.2021
- Impfdatum
- 26.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Nervousness
Vomiting
Symptomtext
Patient vomited about 5 minutes after receiving vaccine. She said she thought maybe her blood pressure had dropped because she felt very nervous about getting the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 26.06.2021
- Impfdatum
- 25.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site swelling
Injection site warmth
Symptomtext
Woke up 3 am with injection site/arm very swollen. Very warm .Site muscle sore.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Rheumatoid arthritis
- Vorgeschichte
- -
- Andere Medikamente
- - BC Arthritis
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 25.06.2021
- Impfdatum
- 25.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hypoaesthesia
Nervousness
Symptomtext
The patient felt dizzy after getting vaccine (about 1 minute). Before getting vaccine he said he felt nervous with the syringe.He said he felt dizzy and his hands are numbing. We let him sit down and drink some water. He felt fine after 15 minutes and he left.
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
- MI
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 25.06.2021
- Impfdatum
- 23.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fall
Symptomtext
After 5 minutes of administering vaccine, the patient got dizzy and fell from chair on to the floor. He was not hurt and head did not hit the ground. He was able to sit back on the chair. He informed that he gets little dizzy after getting any vaccine and feels low blood pressure but this time he felt too much dizziness. Local state police was informed in case if we needed any help for paramedics. He called his dad. He was feeling better after sometime and went with his dad.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- not known
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- Do not know
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 24.06.2021
- Impfdatum
- 11.06.2021
- Beginn
- 20.06.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site mass
Injection site pruritus
Injection site swelling
Symptomtext
COVID ARM- PATIENT DEVELOPED A RED, SWOLLEN, ITCHY LUMP AT INJECTION SITE WEEKS AFTER VACCINATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- GERD, HIGH CHOLESTEROL
- Andere Medikamente
- PROPRANOLOL ER 80 MG, PANTOPRAZOLE DR 40MG, ATORVASTATIN 20 MG
- Allergien
- SULFA CLARITHROMYCIN, CODIENE, OPIOIDS
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 24.06.2021
- Impfdatum
- 22.06.2021
- Beginn
- 22.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Pain in extremity
Symptomtext
Patient received Moderna Vaccine instead of Pfizer for her second shot. She only reported a sore arm and otherwise is doing fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 24.06.2021
- Impfdatum
- 17.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Asthenia
Chills
Dermatitis
Dysstasia
Erythema
Gait disturbance
Genital erythema
Genital tract inflammation
Headache
Hypoaesthesia
Injection site pain
Muscle spasms
Muscle twitching
Musculoskeletal stiffness
Pain
Photopsia
Pyrexia
Symptomtext
Within 12 hours of the dosage typical symptoms reported such as as body aches, mild fever, chills, headache, injection site soreness were experienced. Following that for 12-48 hours following the vaccine administration, severe burning pain was felt in joints and throughout the body. Red inflamed skin was seen on hands, genital area. Visible twitching of face and arm, and leg muscles were seen. Numbness in left side of face was experienced. Severe weakness and inability to lift objects, weakness leading to difficulty standing and walking, spasm in muscles of back and legs, arms, and hands, stiffness in neck, blurred and shifting vision, flashes of light in vision, Etc.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Post-menopausal due to complete hysterectomy. Genital herpes and Epstein Barr shown in blood tests.
- Andere Medikamente
- Estradiol 1mg, Aspirin 82mg, multivitamin and mineral supplement, B-Complex vitamin supplement.
- Allergien
- Penicillin/Amoxicillin, Ciprofloxin Food sensitivity test shows reaction to eggs and dairy products.
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 23.06.2021
- Impfdatum
- 16.06.2021
- Beginn
- 22.06.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Diarrhoea
Dizziness
Fatigue
Headache
Vomiting
Symptomtext
approximately 6 days following my second COVID 19 dose, i woke up in the morning with dizziness which progressed throughout the day. The dizziness resulted in vomiting, diarrhea, headache, weakness and exhaustion by the end of the day. I do feel better today (that was yesterday) although slightly dizzy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 22.06.2021
- Impfdatum
- 22.06.2021
- Beginn
- 22.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Vision blurred
Symptomtext
NAUSEA, DIZZINESS, BLURRED VISION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 22.06.2021
- Impfdatum
- 14.06.2021
- Beginn
- 22.06.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Swollen lump that is red and hurts to touch at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Women?s multivitamin
- Allergien
- Some fruits like apples, bananas and pears.
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 21.06.2021
- Impfdatum
- 17.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site induration
Injection site pain
Injection site rash
Injection site warmth
Pain
Symptomtext
Woke up next morning with hard lump around deltoid along with, red burning rash from injection site radiating down to elbow. Rash along biceps and lateral upper arm. Stinging sensation when arm is bumped or upon touching. Injection site was red, hot and hard the next morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 20.06.2021
- Impfdatum
- 20.06.2021
- Beginn
- 20.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Dizziness
Hyperhidrosis
Pallor
Symptomtext
within 5 minutes, became light headed and very sweaty. blood pressure 78/50 taken twice on our automatic cuff. got pale, felt weak. got some color back by the time the medics arrived.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 18.06.2021
- Impfdatum
- 17.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Peripheral swelling
Pruritus
Skin warm
Symptomtext
pt experiencing diffuse swelling and itching in vaccinated arm (right) pt also reports headache and the arm is warm to the touch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- none reported
- Allergien
- None listed
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 18.06.2021
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Pruritus
Skin warm
Symptomtext
injected arm is swollen, warm to the touch, and slightly itchy hours after the injection. The swelling is about 2.5 inch X 2 inch and it is pink in color.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 17.06.2021
- Impfdatum
- 17.06.2021
- Beginn
- 17.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Erythema
Oral pruritus
Pruritus
Rash macular
Symptomtext
About 20 minutes after patient received the vaccine her face appeared red and blotchy. Patient stated itching all over her body and itching in the mouth. Patient was advised to go to emergency department (ED) at Hospital, 1.5 blocks away from the store. Pharmacy staff contacted patient about a half hour later and patient stated that she was in the ED being checked out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oral pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 17.06.2021
- Impfdatum
- 15.06.2021
- Beginn
- 17.06.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Symptomtext
Rash across neck and chest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroid Disease
- Andere Medikamente
- Levothyroxine
- Allergien
- Possible Gluten allergy but can still consume Gluten lightly according to doctor.
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 16.06.2021
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Erythema
Nausea
Urticaria
Symptomtext
After administering the 1st Moderna vaccine patient immediately said she felt faint. She did faint for about 5 seconds, when she became alert she said she felt nauseous. 911 was called. Patient started to look red in the face and arms like hives were starting. Firefighters arrived and gave her IV Benadryl and an ambulance took her to the nearest hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes
- Andere Medikamente
- -
- Allergien
- Aspirin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 16.06.2021
- Impfdatum
- 13.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Nausea
Pain
Pruritus
Pyrexia
Rash pruritic
Sleep disorder
Urticaria
Symptomtext
Headache within a few hours that lasted for 3 days; Overall achy feeling within 12 hours and last for 2 days; Nausea within 12 hours and lasted for about 24 hours; Low grade fever about 8 hours (normal temperature is usually 97.8-98.6. temp was 99.8-100.5) Fever lasted for about 36 hours. Extremely itchy hives/rash began about 54 hours following the 2nd shot. Itching started on scalp and small patches on right arm and each leg. Itchy actually woke me up out of a deep sleep. Today it has spread to back of thighs, neck and several other smaller patches have popped up all over my body. No breathing problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None so far
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Allergy induced Asthma
- Andere Medikamente
- B12 B Complex Vitamin D Magnesium Claritin
- Allergien
- Sensitive to scented products - can causes rashes, migraines Sensitive to latex gloves - can cause localized rash if worn more then a short time No medication allergies that I'm aware of
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 14.06.2021
- Impfdatum
- 14.06.2021
- Beginn
- 14.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Symptomtext
Patient started calling out for help within minutes of receiving vaccine and she reported sweating and momentary dizziness. She was given water and was asked to sit down for a total of 30 minutes. She said that she had just eaten before coming to the pharmacy but was fasting previous prior to that. She claimed that she felt better but we did not feel that it was safe for her to drive home. Her emergency contact was called and he came and picked patient up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None performed at the pharmacy
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- No drug allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 12.06.2021
- Impfdatum
- 12.06.2021
- Beginn
- 12.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Patient developed light headedness and almost fainted within minutes of receiving the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 12.06.2021
- Impfdatum
- 11.06.2021
- Beginn
- 11.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Injection site pain
Symptomtext
Vaccine administered from refrigerated vial that was approximately 14 hours post expiration. Recipient of vaccine notified of error on 6/11/21. No adverse reaction noted on 6/22/21. Follow up with customer over phone done at 10:00am 6/12/21. Customer stated arm was sore at injection site but no further adverse reaction or complaints noted. Customer did state that he does not have a PCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None noted
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 13.12.2023
- Impfdatum
- 27.06.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 35,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Deafness
Tinnitus
Symptomtext
Tinnitus bilateral
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deafness
- Hospital-Tage
- -
- Labordaten
- Ears and hearing checked spring of 2023. Ears look normal. Minor hearing loss.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraine
- Andere Medikamente
- Synthroid and estradiol
- Allergien
- Penicillin and erythromycin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.06.2023
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2022
- Tage bis Beginn
- 365,0
- Dosis
- 2
- 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 2 vaccines Moderna 6/26/21 lot# 051C21A; Moderna 7/27/21 Lot# 051C21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 03.04.2023
- Impfdatum
- 27.07.2021
- Beginn
- 02.04.2023
- Tage bis Beginn
- 614,0
- 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 vaccine breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID test on 4/2/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 20.01.2023
- Impfdatum
- 29.07.2021
- Beginn
- 22.12.2022
- Tage bis Beginn
- 511,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
SARS-CoV-2 test positive
Symptomtext
12/22/22 presents to ED for "cough". PMHx of "renal transplant"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 12/22/22 SARS-CoV-2 (COVID-19) detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 66,0
- Geschlecht
- U
- Eingang
- 22.11.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event) in a 66-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event) outcome was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- U
- Eingang
- 22.11.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.) and NO ADVERSE EVENT (No adverse event) in a 27-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last year on 12Nov2021 with expiry date on 08-Nov-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last year on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last year on 12Nov2021 with expiry date on 08-Nov-2021) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.). No concomitant medications were reported. It was reported that patient received the Monovalent expired dose of vaccine, it was first booster dose of Moderna COVID-19 vaccine. The vial size was 5.5 ml. The vial was initially stored in the refrigerator on 12-Nov-2021. The vial did not undergo any temperature excursions. No treatment details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 28,0
- Geschlecht
- U
- Eingang
- 22.11.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021; No adverse event; patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event) in a 28-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021). No concomitant medications were reported. It was reported that total 12 patients received the Monovalent expired dose of vaccine, it was their first booster dose of Moderna COVID-19 vaccine. There were 12 doses with vial size 5.5 ml. The vial was initially stored in the refrigerator on 12-Nov-2021. The vial did not undergo any temperature excursions. No treatment details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- U
- Eingang
- 22.11.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Vaccine expiry date was 08-Nov-2021, the vial was initially stored in the refrigerator on 12-Nov-2021; No adverse event; Vaccine expiry date was 08-Nov-2021, the vaccine was administered on 12-Nov-2021; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine expiry date was 08-Nov-2021, the vaccine was administered on 12-Nov-2021), PRODUCT STORAGE ERROR (Vaccine expiry date was 08-Nov-2021, the vial was initially stored in the refrigerator on 12-Nov-2021) and NO ADVERSE EVENT (No adverse event) in a 46-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine expiry date was 08-Nov-2021, the vaccine was administered on 12-Nov-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expiry date was 08-Nov-2021, the vial was initially stored in the refrigerator on 12-Nov-2021) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine expiry date was 08-Nov-2021, the vaccine was administered on 12-Nov-2021), PRODUCT STORAGE ERROR (Vaccine expiry date was 08-Nov-2021, the vial was initially stored in the refrigerator on 12-Nov-2021) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Vaccine expiry date was 08-Nov-2021, the vaccine was administered on 12-Nov-2021) and PRODUCT STORAGE ERROR (Vaccine expiry date was 08-Nov-2021, the vial was initially stored in the refrigerator on 12-Nov-2021). No concomitant drug was reported. Vial size was reported as 5.5 ml. The vial did not undergo any temperature excursions. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- U
- Eingang
- 22.11.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021; No adverse event; patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event) in a 69-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021). Concomitant drugs were not reported. It was reported that the monovalent vial of size 5.5 ml was initially stored in refrigerator on 12-Nov-2021 The vial did not underwent any temperature excursion. Treatment medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- U
- Eingang
- 22.11.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021; No adverse event; Patient got 1 dose of Moderna COVID-19 vaccine last yr on 12-Nov-2021 with expiry date 08-Nov-2021; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient got 1 dose of Moderna COVID-19 vaccine last yr on 12-Nov-2021 with expiry date 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event) in a 62-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient got 1 dose of Moderna COVID-19 vaccine last yr on 12-Nov-2021 with expiry date 08-Nov-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient got 1 dose of Moderna COVID-19 vaccine last yr on 12-Nov-2021 with expiry date 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Patient got 1 dose of Moderna COVID-19 vaccine last yr on 12-Nov-2021 with expiry date 08-Nov-2021) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021). Concomitant drugs were not reported. It was reported that the monovalent vial of size 5.5 ml was initially stored in refrigerator on 12-Nov-2021. The vial did not underwent any temperature excursion. Treatment medications were not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- U
- Eingang
- 22.11.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Dose administered after 30-day Use By Date or after manufacturer date of expiry; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date or after manufacturer date of expiry) and NO ADVERSE EVENT (No adverse event) in a 65-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date or after manufacturer date of expiry). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date or after manufacturer date of expiry) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date or after manufacturer date of expiry). No concomitant medication was reported. No treatment medication was reported. The vial size was of 5.5 mL and was initially stored in the refrigerator on 12-Nov-2021. The vial did not undergo any temperature excursions. The patient received the first booster dose of Moderna vaccine on 12-Nov-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- U
- Eingang
- 22.11.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.; No adverse event; 12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.) and NO ADVERSE EVENT (No adverse event) in a 55-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.). No concomitant medications was reported. It was reported that patient received the Monovalent expired dose of vaccine, it was first booster dose of Moderna COVID-19 vaccine. The vial size was 5.5 ml. The vial was initially stored in the refrigerator on 12-Nov-2021. The vial did not undergo any temperature excursions. No treatment medications was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 60,0
- Geschlecht
- U
- Eingang
- 22.11.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.; No adverse event; patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.) and NO ADVERSE EVENT (No adverse event) in a 60-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021 and administered on 12-Nov-2021.). No concomitant medications were reported. It was reported that patient received the Monovalent expired dose of vaccine, it was first booster dose of Moderna COVID-19 vaccine. The vial size was 5.5 ml. The vial was initially stored in the refrigerator on 12-Nov-2021. The vial did not undergo any temperature excursions. No treatment details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 73,0
- Geschlecht
- U
- Eingang
- 22.11.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021; No adverse event; patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event) in a 73-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021). Concomitant drugs were not reported. It was reported that the monovalent vial of size 5.5 ml was initially stored in refrigerator on 12-Nov-2021 The vial did not underwent any temperature excursion. Treatment medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- U
- Eingang
- 22.11.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry; No adverse event; 12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry), PRODUCT STORAGE ERROR (12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry) and NO ADVERSE EVENT (No adverse event) in a 69-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry), PRODUCT STORAGE ERROR (12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry) and PRODUCT STORAGE ERROR (12 patients got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021./ Dose administered after 30-day Use By Date or after manufacturer date of expiry). No concomitant medications were reported. Dose administered after 30-day Use By Date or after manufacturer date of expiry Vial size was reported as 5.5 mL On 12-Nov-2021, the vial was initially stored in the refrigerator The vial did not undergo any temperature excursions. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- U
- Eingang
- 22.11.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021; No adverse event; patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event) in a 69-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021), PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (patient got 1 dose of Moderna Covid-19 vaccine last yr on 12Nov2021 with expiry date on 08-Nov-2021) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator was 12-Nov-2021, product expiry date 08-Nov-2021). Concomitant drugs were not reported. It was reported that the monovalent vial of size 5.5 ml was initially stored in refrigerator on 12-Nov-2021 The vial did not underwent any temperature excursion. Treatment medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 07.10.2022
- Impfdatum
- 18.05.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 75,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Biopsy bone marrow abnormal
Biopsy kidney abnormal
Blood cholesterol increased
Blood test abnormal
Light chain analysis increased
Plasma cell myeloma
Protein total
Renal disorder
Symptomtext
MULTIPLE MYLOMA!!!!!! Im disgusted at the reponse of the government about this vaccine. You had most americans vaccinated and many (TONS) are now experiencing CANCER, HEART ISSUES, NEUROPATHY. THE GOVERNMENT SHOULD TAKE RESPONSIBLITY LIKE AT LAKE LE JEUNE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy bone marrow abnormal
- Hospital-Tage
- -
- Labordaten
- BLOOD TEST WITH INCREASED KAPPA LIGHT CHAIN IN THE BLOOD. KIDNEY AFFECTED WITH 3+ PROTEIN CHOLESTEROL 425 TRANSLOCATION OF 11;14 KIDNEY BIOPSY CONFIRMING DIAGNOSIS BONE MARROW BIOPSY CONFIRMING DIAGNOSIS
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 24.07.2021
- Beginn
- 08.08.2022
- Tage bis Beginn
- 380,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
hospitalization
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 21.07.2022
- Impfdatum
- 10.06.2021
- Beginn
- 21.07.2022
- Tage bis Beginn
- 406,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
hospitalization
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.06.2022
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 08-Nov-2021, moved to refrigerator on 11-Nov-2021 and 25-Nov-2021, Administered on 16-Dec-2021; Vaccine expired on 08-Nov-2021 and was administered on 16-Dec-2021; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 08-Nov-2021 and was administered on 16-Dec-2021) and PRODUCT STORAGE ERROR (Vaccine expired on 08-Nov-2021, moved to refrigerator on 11-Nov-2021 and 25-Nov-2021, Administered on 16-Dec-2021) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Dec-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 08-Nov-2021 and was administered on 16-Dec-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 08-Nov-2021, moved to refrigerator on 11-Nov-2021 and 25-Nov-2021, Administered on 16-Dec-2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 08-Nov-2021 and was administered on 16-Dec-2021) and PRODUCT STORAGE ERROR (Vaccine expired on 08-Nov-2021, moved to refrigerator on 11-Nov-2021 and 25-Nov-2021, Administered on 16-Dec-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided by the reporter. Vaccines were moved to the refrigerator on 11-Nov-2021 and 25-Nov-2021. Treatment information was not provided. This case was linked to MOD-2022-570635, MOD-2022-570637, MOD-2022-570643, MOD-2022-578379 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.06.2022
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 08 Nov 2021, moved to refrigerator on 11 Nov 2021 and 25 Nov 2021, Administered on 15 DEC 2021; Vaccine expired on 08-Nov-2021 and was administered on 15-Dec-2021; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 08-Nov-2021 and was administered on 15-Dec-2021) and PRODUCT STORAGE ERROR (Vaccine expired on 08 Nov 2021, moved to refrigerator on 11 Nov 2021 and 25 Nov 2021, Administered on 15 DEC 2021) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Dec-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 08-Nov-2021 and was administered on 15-Dec-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 08 Nov 2021, moved to refrigerator on 11 Nov 2021 and 25 Nov 2021, Administered on 15 DEC 2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 08-Nov-2021 and was administered on 15-Dec-2021) and PRODUCT STORAGE ERROR (Vaccine expired on 08 Nov 2021, moved to refrigerator on 11 Nov 2021 and 25 Nov 2021, Administered on 15 DEC 2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications details were not reported by the reporter. Date moved to refrigeration reported as 11-Nov-2021 and 25-Nov-2021. Treatment details was not reported by the reporter. This case was linked to MOD-2022-570635, MOD-2022-570637, MOD-2022-570643, MOD-2022-578385 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 24.05.2022
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 08-Nov-2021 and moved to refrigeration on 25-Nov-2021 and administered on 26-Nov-2021; Vaccine expired on 08-Nov-2021 and was administered on 26-Nov-2021; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT STORAGE ERROR (Vaccine expired on 08-Nov-2021 and moved to refrigeration on 25-Nov-2021 and administered on 26-Nov-2021) and EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 08-Nov-2021 and was administered on 26-Nov-2021) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 26-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 08-Nov-2021 and was administered on 26-Nov-2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 08-Nov-2021 and moved to refrigeration on 25-Nov-2021 and administered on 26-Nov-2021). At the time of the report, PRODUCT STORAGE ERROR (Vaccine expired on 08-Nov-2021 and moved to refrigeration on 25-Nov-2021 and administered on 26-Nov-2021) and EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 08-Nov-2021 and was administered on 26-Nov-2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. No treatment information was provided. Vaccine expired on 08-Nov-2021 and moved to refrigeration on 25-Nov-2021 and administered on 26-Nov-2021 This case was linked to MOD-2022-570635, MOD-2022-570643 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 24.05.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 08 Nov 2021, moved to refrigerator on 11 Nov 2021, Administered on 12 Nov 2021; Dose administered after expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after expiration date) and PRODUCT STORAGE ERROR (Vaccine expired on 08 Nov 2021, moved to refrigerator on 11 Nov 2021, Administered on 12 Nov 2021) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 08 Nov 2021, moved to refrigerator on 11 Nov 2021, Administered on 12 Nov 2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after expiration date) and PRODUCT STORAGE ERROR (Vaccine expired on 08 Nov 2021, moved to refrigerator on 11 Nov 2021, Administered on 12 Nov 2021) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Date moved to refrigeration 11 Nov 2021. No treatment information was reported. This case was linked to MOD-2022-570637, MOD-2022-570643 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 23.12.2021
- Beginn
- 19.05.2022
- Tage bis Beginn
- 147,0
- Dosis
- 2
- Route/Site
- IM / -
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
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 04.03.2022
- Impfdatum
- 25.06.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 195,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bladder cancer
Bladder neoplasm
Computerised tomogram abdomen abnormal
Cystoscopy abnormal
Pathology test
Small cell carcinoma
Symptomtext
2/16/22 Diagnosed with rare bladder cancer 6 months after vaccination (Invasive, High-Grade Neuroendorcrine (Small Cell) Carcinoma). No family history of cancer and no other risk factors such as smoking or working in chemical industry.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bladder cancer
- Hospital-Tage
- -
- Labordaten
- 1/19/22 CT scan of abdomen shows tumor in bladder 1/28/22 Cystoscopy is done to remove tumor 2/16/22 Pathology confirms presence and type of carcinoma
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 27.02.2022
- Impfdatum
- 29.06.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 159,0
- Dosis
- 2
- 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
Event occurred after 2nd vaccine; breakthrough case admission.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 12/5/21 COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 24.07.2021
- Beginn
- 31.07.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
2nd dose given one week from the 1st dose; This spontaneous case was reported by a pharmacist and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose given one week from the 1st dose) in a 33-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 078C21A and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 24-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milligram. On 31-Jul-2021, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .5 milliliter. On 31-Jul-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose given one week from the 1st dose). On 31-Jul-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose given one week from the 1st dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications were not provided by reporter. Treatment information was not provided by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 24.07.2021
- Beginn
- 24.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Herpes zoster
Oral mucosal blistering
Tongue blistering
Symptomtext
Her doctor diagnosed it as shingles; She started with blisters on her tongue.; blisters in her mouth; She also had blisters on her chin as well on same day; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of TONGUE BLISTERING (She started with blisters on her tongue.), ORAL MUCOSAL BLISTERING (blisters in her mouth), BLISTER (She also had blisters on her chin as well on same day) and HERPES ZOSTER (Her doctor diagnosed it as shingles) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 24-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 24-Jul-2021, the patient experienced TONGUE BLISTERING (She started with blisters on her tongue.), ORAL MUCOSAL BLISTERING (blisters in her mouth) and BLISTER (She also had blisters on her chin as well on same day). On an unknown date, the patient experienced HERPES ZOSTER (Her doctor diagnosed it as shingles). At the time of the report, TONGUE BLISTERING (She started with blisters on her tongue.), ORAL MUCOSAL BLISTERING (blisters in her mouth), BLISTER (She also had blisters on her chin as well on same day) and HERPES ZOSTER (Her doctor diagnosed it as shingles) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications provided. No treatment medications provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blister
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 12.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine used) in a 28-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Jul-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine used). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired vaccine used) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medication were not reported. Treatment medications were not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 12.07.2021
- Beginn
- 12.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Gave 1 shot 1 day past BuD; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Gave 1 shot 1 day past BuD) in a 23-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Gave 1 shot 1 day past BuD). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Gave 1 shot 1 day past BuD) had resolved. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant product use was provided by the reporter. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 12.07.2021
- Beginn
- 12.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Gave 1 shot 1 day past; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Gave 1 shot 1 day past) in a 48-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Jul-2021 at 10:46 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) at an unspecified dose. On 12-Jul-2021 at 12:05 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Gave 1 shot 1 day past). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Gave 1 shot 1 day past) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) and mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment information were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 22.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vaccination site erythema
Symptomtext
red mark at the injection site; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE ERYTHEMA (red mark at the injection site) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 008D21A) for COVID-19 vaccination. Concomitant products included LEVOTHYROXINE for an unknown indication. On 22-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced VACCINATION SITE ERYTHEMA (red mark at the injection site). At the time of the report, VACCINATION SITE ERYTHEMA (red mark at the injection site) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) and mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown. No information about treatment medication was provided by reporter. This case was linked to MOD-2021-263826 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 22.04.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Interchange of vaccine products
Symptomtext
Patient got a covid-19 after first dose of the Pfizer vaccine; Patient got a Pfizer vaccine on April 2021 and a Moderna vaccine on June 2021; This spontaneous case was reported by a pharmacist and describes the occurrence of INTERCHANGE OF VACCINE PRODUCTS (Patient got a Pfizer vaccine on April 2021 and a Moderna vaccine on June 2021) and COVID-19 (Patient got a covid-19 after first dose of the Pfizer vaccine) in a 19-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for COVID-19 vaccination. No Medical History information was reported. On 22-Apr-2021, the patient received first dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (Intramuscular) 1 dosage form. On 23-Jun-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In April 2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Patient got a Pfizer vaccine on April 2021 and a Moderna vaccine on June 2021). On an unknown date, the patient experienced COVID-19 (Patient got a covid-19 after first dose of the Pfizer vaccine). At the time of the report, INTERCHANGE OF VACCINE PRODUCTS (Patient got a Pfizer vaccine on April 2021 and a Moderna vaccine on June 2021) had resolved and COVID-19 (Patient got a covid-19 after first dose of the Pfizer vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medication was received by the patient No Treatment was received by the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 05.05.2021
- Beginn
- 19.07.2021
- Tage bis Beginn
- 75,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
This spontaneous case reported by a pharmacist, describes the occurrence of inappropriate schedule of product administration (more than 2-month interval between both doses of Moderna COVID-19 vaccine) in a 22-year-old male patient who received mRNA-1273 (Moderna COVID-19 vaccine, batch/lot# 051C21A) for COVID-19 immunization. No medical history reported. On May 5, 2021, patient received the first dose of mRNA-1273 (Moderna COVID-19 vaccine), intramuscular; 1 dosage form. On Jul 19, 2021, patient experienced inappropriate schedule of product administration (more than 2-month interval between both doses of Moderna COVID-19 vaccine). At the time of the report, inappropriate schedule of product administration (more than 2-month interval between both doses of Moderna COVID-19 vaccine): resolved. The action taken with mRNA-1273 (Moderna COVID-19 vaccine), intramuscular: unknown. The reporter did not provide any causality assessments, concomitant medication or treatment information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 18.06.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Use of an expired vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Use of an expired vaccine) in a 47-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 16-Jul-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Use of an expired vaccine). On 16-Jun-2021, EXPIRED PRODUCT ADMINISTERED (Use of an expired vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant information was reported. No treatment information was reported. Reporter has stated that patient has received his second dose of expired vaccine after day of its expiry in fridge. Most recent FOLLOW-UP information incorporated above includes: On 31-Jul-2021: Follow up received on 31-07-2021, contains new information. Updated patient gender as female.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 12.07.2021
- Beginn
- 12.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
The pharmacist reported that his pharmacy used a vial of the Moderna COVID-19 vaccine that had been refrigerated for 31 days On the 31st day (12JUL2021) administered doses of the Moderna COVID-19 vaccine from the vial; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The pharmacist reported that his pharmacy used a vial of the Moderna COVID-19 vaccine that had been refrigerated for 31 days On the 31st day (12JUL2021) administered doses of the Moderna COVID-19 vaccine from the vial) in a 33-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Jul-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (The pharmacist reported that his pharmacy used a vial of the Moderna COVID-19 vaccine that had been refrigerated for 31 days On the 31st day (12JUL2021) administered doses of the Moderna COVID-19 vaccine from the vial). On 12-Jul-2021, EXPIRED PRODUCT ADMINISTERED (The pharmacist reported that his pharmacy used a vial of the Moderna COVID-19 vaccine that had been refrigerated for 31 days On the 31st day (12JUL2021) administered doses of the Moderna COVID-19 vaccine from the vial) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant drug details were reported. No treatment details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 12.07.2021
- Beginn
- 12.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Four patients were administered doses of the Moderna COVID-19 vaccine from an expired vial.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Four patients were administered doses of the Moderna COVID-19 vaccine from an expired vial.) in a 33-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Jul-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Four patients were administered doses of the Moderna COVID-19 vaccine from an expired vial.). On 12-Jul-2021, EXPIRED PRODUCT ADMINISTERED (Four patients were administered doses of the Moderna COVID-19 vaccine from an expired vial.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were mentioned. No treatment details were reported. Most recent FOLLOW-UP information incorporated above includes: On 28-Jul-2021: Follow up received contains updated patient-1 demographics: Patient initials, age, gender, race and ethinicity; Updated anatomical site of vaccination; On 28-Jul-2021: Follow up received contains updated patient -2 demographics: Patient initials, age, gender, race and ethinicity; Updated anatomical site of vaccination; On 28-Jul-2021: Follow up received contains no new information (NNI) On 28-Jul-2021: Follow up received contains no new information (NNI)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 37,0
- Geschlecht
- U
- Eingang
- 26.02.2022
- Impfdatum
- 08.07.2021
- Beginn
- 08.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
received 1st dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours when administered.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received 1st dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours when administered.) in a 37-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (received 1st dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours when administered.). On 08-Jul-2021, EXPIRED PRODUCT ADMINISTERED (received 1st dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours when administered.) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 09-Jul-2021: Follow up received on 09-Jul-2021 and does not contain any new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 39,0
- Geschlecht
- U
- Eingang
- 26.02.2022
- Impfdatum
- 08.07.2021
- Beginn
- 08.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Medication error
Symptomtext
medication error; received 1st dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours when administered.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received 1st dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours when administered.) and MEDICATION ERROR (medication error) in a 39-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (received 1st dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours when administered.). On an unknown date, the patient experienced MEDICATION ERROR (medication error). At the time of the report, EXPIRED PRODUCT ADMINISTERED (received 1st dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours when administered.) and MEDICATION ERROR (medication error) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medication were reported. Treatment medication was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 09.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
dose given was beyond the use date (BUD) of 8July2021; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (dose given was beyond the use date (BUD) of 8July2021) in a 57-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (dose given was beyond the use date (BUD) of 8July2021). On 09-Jul-2021, EXPIRED PRODUCT ADMINISTERED (dose given was beyond the use date (BUD) of 8July2021) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered EXPIRED PRODUCT ADMINISTERED (dose given was beyond the use date (BUD) of 8July2021) to be not applicable. Concomitant medications were not reported. This case was linked to MOD21-119255, MOD21-119243 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 12-Jul-2021: Updated query has been received from Safety and mentioned in inarrative. On 14-Jul-2021: Follow up document received on 14-UL-2021 and contains No New Information; Sender's Comments: This report refers to a case of Expired vaccine use for mRNA-1273, lot 051C21A with no associated AEs. According to Regulatory Authority's module this is an invalid case.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 09.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Device connection issue
Underdose
Symptomtext
Syringe connection issue; Vaccine underdose; This spontaneous case was reported by a pharmacist and describes the occurrence of DEVICE CONNECTION ISSUE (Syringe connection issue) and UNDERDOSE (Vaccine underdose) in a 25-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Jul-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Jul-2021, the patient experienced DEVICE CONNECTION ISSUE (Syringe connection issue) and UNDERDOSE (Vaccine underdose). At the time of the report, DEVICE CONNECTION ISSUE (Syringe connection issue) and UNDERDOSE (Vaccine underdose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Device connection issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 24,0
- Geschlecht
- U
- Eingang
- 26.02.2022
- Impfdatum
- 08.07.2021
- Beginn
- 08.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
received 2nd dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received 2nd dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours) in a 24-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Jul-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (received 2nd dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours). On 08-Jul-2021, EXPIRED PRODUCT ADMINISTERED (received 2nd dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product information, if any, was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 09.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
Pharmacist said that they have 5 refrigerated vials that went the beyond use date of 8July2021; second dose given was beyond the use date (BUD) of 8July2021; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (second dose given was beyond the use date (BUD) of 8July2021) and PRODUCT STORAGE ERROR (Pharmacist said that they have 5 refrigerated vials that went the beyond use date of 8July2021) in a 58-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Jul-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (second dose given was beyond the use date (BUD) of 8July2021). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Pharmacist said that they have 5 refrigerated vials that went the beyond use date of 8July2021). On 09-Jul-2021, EXPIRED PRODUCT ADMINISTERED (second dose given was beyond the use date (BUD) of 8July2021) had resolved. At the time of the report, PRODUCT STORAGE ERROR (Pharmacist said that they have 5 refrigerated vials that went the beyond use date of 8July2021) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant Medications were reported. Pharmacist said that 1 vial was used and 4 patients received a dose from a vial today 9-July-2021 and that was beyond the use date of 8- July-2021. Pharmacist said that the 4 other vials are still sealed, unused and for disposal. The pharmacist said that the patients are not yet aware of the concern. No treatment information was provided by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 12-Jul-2021: Live follow-up information received on 12-JUL-2021 contains non-significant information. On 20-Jul-2021: Follow up received and the event outcome has been updated from unknown to resolved with respect to initial document.; Sender's Comments: Causality for events Expired product administered and Product storage error is not applicable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 56,0
- Geschlecht
- U
- Eingang
- 26.02.2022
- Impfdatum
- 08.07.2021
- Beginn
- 08.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Received 1st dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours when administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received 1st dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours when administered) in a 56-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received 1st dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours when administered). On 08-Jul-2021, EXPIRED PRODUCT ADMINISTERED (Received 1st dose of the Moderna COVID-19 vaccine from a vial that had been first punctured on 07Jul2021 @ 3:42p with the syringe having been at room temperature approximately 24 hours when administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant products were reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.02.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Administered 10 doses of Moderna COVID Vaccine after the 30 day refrigerator guideline; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 08-Jul-2021 and was forwarded to Moderna on 08-Jul-2021. Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered 10 doses of Moderna COVID Vaccine after the 30 day refrigerator guideline) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered 10 doses of Moderna COVID Vaccine after the 30 day refrigerator guideline). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered 10 doses of Moderna COVID Vaccine after the 30 day refrigerator guideline) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Medical history and Concomitant medications details are not provided by the Reporter. Vial was first moved to the fridge on 03JUN2021. On 05JUL2021,06JUL2021 and 07JUL 2021 10 doses of Moderna COVID Vaccine was administered after the 30 day refrigerator guideline. Doses were meant to be expired on Sunday July 4th but overall 10 doses were administered to 10 patients between 05JUL2021 and 07JUL2021 while they were stored in the refrigeration between 35 and 46 Degree F. No treatment information is provided. Most recent FOLLOW-UP information incorporated above includes: On 08-Jul-2021: Follow-up information received on 8 JUL 2021 contains no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 03.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inflammation
Lymphadenopathy
Mastication disorder
Symptomtext
little bit of discomfort if I chewed or spoke; some inflammation of the gland in neck; little bit of swelling on the gland in his neck; This spontaneous case was reported by a consumer and describes the occurrence of LYMPHADENOPATHY (little bit of swelling on the gland in his neck), MASTICATION DISORDER (little bit of discomfort if I chewed or spoke) and INFLAMMATION (some inflammation of the gland in neck) in a 75-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No medical history was provided by the reporter. Concomitant products included AMLODIPINE and ROSUVASTATIN CALCIUM (CRESTOR) for an unknown indication. On 03-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced LYMPHADENOPATHY (little bit of swelling on the gland in his neck), MASTICATION DISORDER (little bit of discomfort if I chewed or spoke) and INFLAMMATION (some inflammation of the gland in neck). At the time of the report, LYMPHADENOPATHY (little bit of swelling on the gland in his neck), MASTICATION DISORDER (little bit of discomfort if I chewed or spoke) and INFLAMMATION (some inflammation of the gland in neck) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inflammation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- AMLODIPINE; CRESTOR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
13 years old (deviation from recommended age group); This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (13 years old (deviation from recommended age group)) in a 13-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Jul-2021, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (13 years old (deviation from recommended age group)). On 06-Jul-2021, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (13 years old (deviation from recommended age group)) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No medical history reported. Concomitant medications were not provided. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 12.06.2021
- Beginn
- 07.07.2021
- Tage bis Beginn
- 25,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Punctured vial was stored at room temperature for over 12 hours; Patient received vaccine after allowed expiry time; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after allowed expiry time) and PRODUCT STORAGE ERROR (Punctured vial was stored at room temperature for over 12 hours) in a 23-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 078C21A and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 07-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 07-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after allowed expiry time). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Punctured vial was stored at room temperature for over 12 hours). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after allowed expiry time) and PRODUCT STORAGE ERROR (Punctured vial was stored at room temperature for over 12 hours) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No relevant concomitant medication was reported. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- U
- Eingang
- 25.02.2022
- Impfdatum
- 03.08.2021
- Beginn
- 13.01.2022
- Tage bis Beginn
- 163,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Mental status changes
SARS-CoV-2 test positive
Symptomtext
01/13/22 presents to ED for "altered mental status". PMHx of "liver cancer and liver cirrhosis"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 01/13/22 SARS-CoV-2 (COVID-19) detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 30.07.2021
- Beginn
- 04.01.2022
- Tage bis Beginn
- 158,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
Hospitalization
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 31,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 17.02.2022
- Impfdatum
- 24.06.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 88,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID 19 case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- COVID PCR positive 09/20/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- A-fib, CAD, GERD, MI, Pulmonary Fibrosis, Hypercholesterolemia, Prostatic Hypertrophy
- Andere Medikamente
- -
- Allergien
- Ampicillin
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 04.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 22,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
Electrocardiogram abnormal
Electrocardiogram normal
Laboratory test
Symptomtext
I have had an undiagnosed Atrial Fibrillation with an official diagnosis on or around 11/26/20. Prior to my booster , it would occur every 4-6 months after it would occur multiple times of month after 11/26/2021. I went to the ER November 3rd because I had been in AF for over 12 hrs. At that time I was prescribed Apixaban 5mg 2x daily and Metoprolol 25mg 1 daily. They performed an EKG and diagnosed Atrial fibrillation. I followed up with the cardiologist on November 8, 2021. Flecainide 100mg 2xdaily was added through follow-ups on January 27, 2022 because the medications were not preventing the onset of AF. I had a follow up on 02/04/2022 and had an EKG. Between those times my medications were adjusted and I was prescribed Flecainide 100mg 2xdaily and at my appointment last week it was reduced to 50 mg 2xdaily. At this point, it is being controlled.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- EKG 11/26/21 Diagnosed Atrial Fibrillation EKG 02/04/2022 everything was normal Labs 11/26/2021 -Not sure of results. I am thinking they are normal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- 1. Hypertension 2. Hyperlipidemia
- Andere Medikamente
- 1. Rosuvastatin Calcium 10mg 1xdaily 2, Losartan Potassium 25mg Daily 3. Coenzyme Q10 100mg Daily 4. Long acting steroid injections in two locations in spine
- Allergien
- 1. Ibuprofen 2. Lisinopril cough
- Vorherige Impfungen
- Moderna 2nd dose VAERS report filed
- Staat
- FL
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 03.07.2021
- Beginn
- 24.01.2022
- Tage bis Beginn
- 205,0
- Dosis
- 2
- Route/Site
- IM / -
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
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 11.05.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 35,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Balance disorder
Gait disturbance
Head discomfort
Laboratory test normal
Tooth loss
Vertigo
Visual impairment
Symptomtext
Severe vertigo one week after vaccine. Turned into an intense vibration in center of head that rattles my eyes so I cannot see clearly and my teeth (I have lost one molar tooth). I can no longer walk without losing my balance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Balance disorder
- Hospital-Tage
- -
- Labordaten
- Does not show up on tests. I have multiple systems effected with no medical history. 2 Doctors are now convinced it can only be from vaccine after process of elimination.
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 19.06.2021
- Beginn
- 18.01.2022
- Tage bis Beginn
- 213,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
ADMITTED TO HOSPITAL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 08.07.2021
- Beginn
- 08.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Patient asked for the Shingrix shot and given the Modera COVID-19 shot instead.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 23.06.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 197,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
incidental finding for patient testing for psych placement
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 03.09.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 115,0
- 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
Breakthrough Case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid + on 12/27/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 30.07.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 154,0
- Dosis
- 1
- Route/Site
- IM / -
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
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 31.07.2021
- Beginn
- 09.09.2021
- Tage bis Beginn
- 40,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deafness
Symptomtext
PATIENT EXPERIENCED HEARING LOSS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deafness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 20.07.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 140,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Exposure during pregnancy
SARS-CoV-2 test positive
Symptomtext
COVID breakthrough. Patient came to hospital on 12/7/21 for delivery of her baby. She was routinely tested for COVID and resulted positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID+ by PCR on 12/7/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 13.08.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 113,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient tested positive for Covid on 12/4/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 06.08.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 52,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Muscle twitching
Symptomtext
Muscles jumping / twitching. Mostly occurs in front thighs, but occasionally other muscles.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Muscle twitching
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 30.11.2021
- Impfdatum
- 01.06.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 182,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase increased
Blood alkaline phosphatase increased
Blood thyroid stimulating hormone
Dermatitis
Hyperthyroidism
Thyroid function test abnormal
Thyroiditis
Thyroxine
Symptomtext
Diffuse dermatitis followed by thyroiditis/hyperthyroidism
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alanine aminotransferase increased
- Hospital-Tage
- -
- Labordaten
- ALT 49, Alk phos 164, TSH <0.01, FT4 3.5 on 11/4/2021 Abnormal TFTR's confirmed 11/22/2021 with clinical hyperthyroidism
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 24.11.2021
- Impfdatum
- 27.07.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 106,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Gallbladder disorder
Symptomtext
No Covid symptoms, had gallbladder issues
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gallbladder disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 23.11.2021
- Impfdatum
- 14.06.2021
- Beginn
- 27.06.2021
- Tage bis Beginn
- 13,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Ear disorder
Herpes zoster
Symptomtext
Activated shingles at only 42 years old. Needed two rounds of acyclovir. Damaged ear. Have had ear infection taking antibiotics for nearly 3 month straight.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 21.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysmenorrhoea
Heavy menstrual bleeding
Ovarian cyst
Polymenorrhoea
Ultrasound ovary abnormal
Ultrasound uterus
Symptomtext
I haven't had an actual period for over a year since I got my IUD. 1 week after the vaccine, I started getting a heavy painful period which lasted 2 weeks, stopped for two weeks, and then continued every two weeks for 3+ months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysmenorrhoea
- Hospital-Tage
- -
- Labordaten
- Ultrasound on uterus and ovaries on 11/12/21. Ultrasound showed a cyst on the left ovary. I had had ovarian cysts for years and have never had it affect my period.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Escitalopram 20 mg Abilify 2 mg Strattera 60 mg Tramadol 50mg omeprazole 20 mg Kyleena IUD
- Allergien
- Pecans Toradol
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 08.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Booster dose Moderna vaccine was administered outside the suggested date taking into consideration the second dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 02.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure measurement
Product administered to patient of inappropriate age
Symptomtext
A 15 year old patient was administered 1st dose of Moderna vaccine/Off-label use; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 28-Oct-2021 and was forwarded to Moderna on 29-Oct-2021. This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (A 15 year old patient was administered 1st dose of Moderna vaccine/Off-label use) in a 15-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The patient's past medical history included Painful ankle and Drug use disorder (History of Drug Use). Concurrent medical conditions included Drug allergy (Tylenol) and Obesity (on 15-02-2020 the weight was 102.4kg on 04-08-2021 the weight was 133.4kg). On 02-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Sep-2021, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (A 15 year old patient was administered 1st dose of Moderna vaccine/Off-label use). On 02-Sep-2021, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (A 15 year old patient was administered 1st dose of Moderna vaccine/Off-label use) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 08-Apr-2021, Blood pressure measurement: elevated (High) ELEVATED BLOOD PRESSURE. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant and treatment medications was not reported. This case was linked to MOD-2021-303426 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure measurement
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210408; Test Name: Blood pressure; Result Unstructured Data: ELEVATED BLOOD PRESSURE
- Aktuelle Erkrankungen
- Drug allergy (Tylenol); Obesity (on 15-02-2020 the weight was 102.4kg on 04-08-2021 the weight was 133.4kg)
- Vorgeschichte
- Medical History/Concurrent Conditions: Drug use disorder (History of Drug Use); Painful ankle
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 24.10.2021
- Impfdatum
- 29.06.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heavy menstrual bleeding
Menstrual disorder
Muscle spasms
Symptomtext
Heavy menstrual bleeding for 9 days accompanied by very painful cramps beginning 3 days after vaccination. For previous 2 years, menstruation had been very light with no painful cramps.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heavy menstrual bleeding
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 22.10.2021
- Impfdatum
- 20.07.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 93,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Cough
SARS-CoV-2 test positive
Symptomtext
Patient came in with generalized weakness and cough. Patient medicating with tylenol. Admitted to Hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 2,0
- Labordaten
- Positive Covid Swab
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- Hypertension
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 21.10.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Administered the 1 st dose of the Moderna COVID-19 Vaccine to a 12 years old female patient; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (Administered the 1 st dose of the Moderna COVID-19 Vaccine to a 12 years old female patient) in a 12-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-Aug-2021, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (Administered the 1 st dose of the Moderna COVID-19 Vaccine to a 12 years old female patient). On 13-Aug-2021, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (Administered the 1 st dose of the Moderna COVID-19 Vaccine to a 12 years old female patient) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant product information was not provided. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 16-Aug-2021: Follow-up Information received contains No Significant Information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 20.10.2021
- Impfdatum
- 09.09.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 33,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
12 hours out of expiration; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (12 hours out of expiration) in a 44-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Oct-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 12-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (12 hours out of expiration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (12 hours out of expiration) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. Treatment information was not provided by the reporter. This case was linked to MOD-2021-350532 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 20.10.2021
- Impfdatum
- 09.09.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 33,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Had received their second dose of the Moderna covid-19 vaccine after the dose had passed the published expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Had received their second dose of the Moderna covid-19 vaccine after the dose had passed the published expiration date) in an 18-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 049E21A and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Oct-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 12-Oct-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Had received their second dose of the Moderna covid-19 vaccine after the dose had passed the published expiration date). On 12-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Had received their second dose of the Moderna covid-19 vaccine after the dose had passed the published expiration date) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications were not reported. Action taken with mRNA-1273 in response to the events was not applicable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 17.10.2021
- Impfdatum
- 22.06.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 74,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abortion spontaneous
Blood test abnormal
Menstruation irregular
Pregnancy
Ultrasound scan abnormal
Urine analysis abnormal
Vaginal haemorrhage
Symptomtext
After the first shot my period suddenly came back after not having one since having my daughter a year before. Then I got the second shot. I became pregnant shortly after. I then had a miscarriage that started with slight bleeding on the 4th. More bleeding on the 5th. Then on the 6th I had to go to my third hospital due to extreme bleeding. I?m now having a period every other week that starts with spotting for 3 days and then bleeding for 5.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abortion spontaneous
- Hospital-Tage
- -
- Labordaten
- Blood, urine, and vaginal ultrasound done on Sept 5th, 2021 proved I was having a miscarriage. More blood, ultrasounds, and pelvic exams on Sept 6th proved a miscarriage.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 15.10.2021
- Impfdatum
- 23.06.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 114,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
I recently discovered that I received 2 separate vaccines for COVID-19. I did not discover this until I went to upload my vaccine status to my company's website and the first shot was Moderna (lot number 051C21A) and the second shot is Pzizer (lot number FA7485). I got my first shot at a pharmacy on June 23, 2021, and my second shot at a different pharmacy on July 21, 2021. I had to go to 2 separate pharmacies because the first one was closed when I went there to receive my second shot so I had to go to the nearest pharmacy. Neither pharmacies noticed this mistake or informed me that they gave me 2 separate shots. I am not a medical professional and I am not sure of the implications of this mistake or how it affects my personal health.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 13.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine was placed in the fridge to that from freezer and expired on 10/11/2021 and was given on 10/12/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- none known
- Andere Medikamente
- None known
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 13.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine had been placed from the freezer and fridge which expired on 10/11/21 and had been given on 10/12/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Taking medications for cholesterol and high blood pressure and levothyroxine
- Andere Medikamente
- None
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 28.09.2021
- Beginn
- 28.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Moderna 3rd dose (additional dose) administered to patient that is not indicated to receive additional dose as patient is not taking any medications and only has history of IBD. Patient did not indicate that she was immunocompromised on consent form.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- IBD (irritable bowel syndrome)
- Vorgeschichte
- Irritable bowel syndrome
- Andere Medikamente
- No medications/prescriptions being taken per patient
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 24.09.2021
- Impfdatum
- 21.05.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 46,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Woke up on the morning of July 6 and felt big lumps under my arm pits then noticed them on my neck and now as time goes by more are appearing all over me 3 months dealing with this 3 doctors been to nobody now's nothing unreal that this happening to me
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- COPD
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 17.09.2021
- Impfdatum
- 28.07.2021
- Beginn
- 28.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 16.09.2021
- Impfdatum
- 01.06.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 106,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
Covid-19 after complete vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 14.09.2021
- Impfdatum
- 07.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Computerised tomogram thorax
Fear
Gait disturbance
Symptomtext
Heavy and tight chest. My chest was so heavy that it was hard to lay down or get up to walk. It was tight all day but worsened when lying down resulting in me staying propped up at night. It was very scary. I contemplated going to the ER but knew how busy they are these days. My chest continued to feel pressure from July 9, 2021 until August 2. I was able to get a CT scan completed during this time and was able to schedule an appointment with a pulmonologist but symptoms had disappeared before I was able to see the doctor due to how far out I had to make the appointment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest discomfort
- Hospital-Tage
- -
- Labordaten
- CT scan on July 19, 2021 at 1:10
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Enlarged pulmonary artery- identified on CT scan Aug. 2020
- Andere Medikamente
- Zyrtec 10mg
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 13.09.2021
- Impfdatum
- 20.07.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 32,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Accidental overdose
Ageusia
Tinnitus
Symptomtext
A ringing on both ears/ tinnitus; second dose seemed like a larger dose than the first; Lost taste/ barely taste/ He can barely taste coffee, can't taste vinegar/ does not have taste; This spontaneous case was reported by a consumer and describes the occurrence of AGEUSIA (Lost taste/ barely taste/ He can barely taste coffee, can't taste vinegar/ does not have taste), TINNITUS (A ringing on both ears/ tinnitus) and ACCIDENTAL OVERDOSE (second dose seemed like a larger dose than the first) in a 56-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 21-Aug-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced AGEUSIA (Lost taste/ barely taste/ He can barely taste coffee, can't taste vinegar/ does not have taste). On an unknown date, the patient experienced TINNITUS (A ringing on both ears/ tinnitus) and ACCIDENTAL OVERDOSE (second dose seemed like a larger dose than the first). At the time of the report, AGEUSIA (Lost taste/ barely taste/ He can barely taste coffee, can't taste vinegar/ does not have taste) and TINNITUS (A ringing on both ears/ tinnitus) outcome was unknown and ACCIDENTAL OVERDOSE (second dose seemed like a larger dose than the first) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medication was reported. No treatment medications were reported Patient wants some medical advice over the situation This case was linked to MOD-2021-305910 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental overdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 13.09.2021
- Impfdatum
- 12.07.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 49,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product dose omission issue
Symptomtext
Missed the second shot 48 days post first vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT DOSE OMISSION ISSUE (Missed the second shot 48 days post first vaccine) in a 61-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Aug-2021, the patient experienced PRODUCT DOSE OMISSION ISSUE (Missed the second shot 48 days post first vaccine). On 30-Aug-2021, PRODUCT DOSE OMISSION ISSUE (Missed the second shot 48 days post first vaccine) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment information was reported. The patient was yet to received second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product dose omission issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 07.09.2021
- Impfdatum
- 19.07.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Administered today from a vial that was punctured more than 12 hours ago; This spontaneous case was reported by a consumer and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered today from a vial that was punctured more than 12 hours ago) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 088D21A and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 16-Aug-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered today from a vial that was punctured more than 12 hours ago). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered today from a vial that was punctured more than 12 hours ago) had resolved. No concomitant medications were reported. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 07.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Inappropriate schedule of product administration
Symptomtext
gave second vaccine dose from the expired vial; first dose of the Moderna COVID-19 vaccine on 07Jul2021 and the second on 20Aug2021; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (gave second vaccine dose from the expired vial) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first dose of the Moderna COVID-19 vaccine on 07Jul2021 and the second on 20Aug2021) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 052E211A. and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (gave second vaccine dose from the expired vial) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first dose of the Moderna COVID-19 vaccine on 07Jul2021 and the second on 20Aug2021). At the time of the report, EXPIRED PRODUCT ADMINISTERED (gave second vaccine dose from the expired vial) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first dose of the Moderna COVID-19 vaccine on 07Jul2021 and the second on 20Aug2021) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant Medications were provided. No Treatment Medications were provided. This case was linked to MOD-2021-133589 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 23.07.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 25,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nasal congestion
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of NASAL CONGESTION (Stuffy nose couple days ago) in a sixty-four-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (Batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-Aug-2021, the patient experienced NASAL CONGESTION (Stuffy nose couple days ago). At the time of the report, NASAL CONGESTION (Stuffy nose couple days ago) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medication of the patient was not reported. No treatment information was provided by the reporter. The patient was scheduled to take his second shot vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nasal congestion
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 02.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate increased
Symptomtext
Adverse event: patient reported rapidly beating heart 6-12 hours after vaccine while sleeping. Extreme concern. Lasted about 20 minutes. Reported to PCP week of 23 Aug 2021. Doctor recommended proceed second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate increased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, DVT/PE
- Andere Medikamente
- Elquis, atenolpl-chlorthal, klor-con, iron, miltivitamin
- Allergien
- Ace-inhibitor (ie zestorectic)
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 07.06.2021
- Beginn
- 10.07.2021
- Tage bis Beginn
- 33,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Patient received 2 doses of the Astra Zeneca vaccine then received 1 dose of the Moderna vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of INTERCHANGE OF VACCINE PRODUCTS (Patient received 2 doses of the Astra Zeneca vaccine then received 1 dose of the Moderna vaccine) in a 37-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. Co-suspect product included non-company product COVID-19 VACCINE NRVV AD (CHADOX1 NCOV-19) (COVID-19 VACCINE ASTRAZENECA) for COVID-19 vaccination. No Medical History information was reported. On 07-Jun-2021, the patient received second dose of COVID-19 VACCINE NRVV AD (CHADOX1 NCOV-19) (COVID-19 VACCINE ASTRAZENECA) (unknown route) dosage was changed to 1 dosage form. On 10-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient received first dose of COVID-19 VACCINE NRVV AD (CHADOX1 NCOV-19) (COVID-19 VACCINE ASTRAZENECA) (unknown route) 1 dosage form. On 10-Jul-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Patient received 2 doses of the Astra Zeneca vaccine then received 1 dose of the Moderna vaccine). On 10-Jul-2021, INTERCHANGE OF VACCINE PRODUCTS (Patient received 2 doses of the Astra Zeneca vaccine then received 1 dose of the Moderna vaccine) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 29.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient administered dose before recommended scheduled vaccine date; This spontaneous case was reported by a consumer and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient administered dose before recommended scheduled vaccine date) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient administered dose before recommended scheduled vaccine date). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient administered dose before recommended scheduled vaccine date) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant and treatment information were reported by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 29-Jul-2021: Follow up received and does not contain any new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 30.06.2021
- Beginn
- 30.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Hypoaesthesia
Symptomtext
arm went numb down to the tips of my fingers/Felt like circulation in my forearm down to my fingers had been cut off/As soon as he injected me with the vaccine, my arm went numb; experienced something very strange/very strange feeling/every now and then I get the weird sensation that it's getting numb again; This spontaneous case was reported by a consumer and describes the occurrence of HYPOAESTHESIA (arm went numb down to the tips of my fingers/Felt like circulation in my forearm down to my fingers had been cut off/As soon as he injected me with the vaccine, my arm went numb) and FEELING ABNORMAL (experienced something very strange/very strange feeling/every now and then I get the weird sensation that it's getting numb again) in a 45-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The medical history was not provided by the reporter. Concomitant products included BUPROPION HYDROCHLORIDE (WELLBUTRIN) for an unknown indication. On 30-Jun-2021 at 11:20 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Jun-2021, the patient experienced HYPOAESTHESIA (arm went numb down to the tips of my fingers/Felt like circulation in my forearm down to my fingers had been cut off/As soon as he injected me with the vaccine, my arm went numb) and FEELING ABNORMAL (experienced something very strange/very strange feeling/every now and then I get the weird sensation that it's getting numb again). At the time of the report, HYPOAESTHESIA (arm went numb down to the tips of my fingers/Felt like circulation in my forearm down to my fingers had been cut off/As soon as he injected me with the vaccine, my arm went numb) and FEELING ABNORMAL (experienced something very strange/very strange feeling/every now and then I get the weird sensation that it's getting numb again) was resolving. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment information, if any, was not provided Most recent FOLLOW-UP information incorporated above includes: On 30-Jun-2021: Addition information included primary reporter address, patient details, Added suspect dose batch number, date and route of administration, Added concomitant medicine, Added event dates and outcome.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling abnormal
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The medical history was not provided by the reporter
- Andere Medikamente
- WELLBUTRIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 19.06.2021
- Beginn
- 19.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
patient received the vaccine from vial 12 hours after the vial was punctured; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received the vaccine from vial 12 hours after the vial was punctured) in a 38-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Jun-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 19-Jun-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received the vaccine from vial 12 hours after the vial was punctured). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received the vaccine from vial 12 hours after the vial was punctured) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 19.06.2021
- Beginn
- 19.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
This spontaneous case reported by a pharmacist, describes the occurrence of administered expired product (received vaccine 12 hours after the vial was punctured) in a 60-year-old male patient who received mRNA-1273 (Moderna COVID-19 vaccine, batch# 051C21A) for COVID-19 immunization. No medical history reported. On Jun 19, 2021, patient received the first dose of mRNA-1273 (Moderna COVID-19 vaccine), intramuscular; 1 dosage form. On Jun 19, 2021, patient administered expired product (received vaccine 12 hours after the vial was punctured). At the time of the report, administered expired product (received vaccine 12 hours after the vial was punctured) outcome: unknown. The action taken with mRNA-1273 (Moderna COVID-19vaccine), intramuscular: unknown. The reporter did not provide any causality assessments, concomitant medication or treatment information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 01.01.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Off label use
Symptomtext
This patient received 1 dose of Pfizer COVID 19 vaccine in January, 2021; This spontaneous case was reported by a pharmacist and describes the occurrence of OFF LABEL USE (This patient received 1 dose of Pfizer COVID 19 vaccine in January, 2021) in a 64-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for COVID-19 vaccination. No Medical History information was reported. In January 2021, the patient received first dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On 24-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced OFF LABEL USE (This patient received 1 dose of Pfizer COVID 19 vaccine in January, 2021). At the time of the report, OFF LABEL USE (This patient received 1 dose of Pfizer COVID 19 vaccine in January, 2021) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Off label use
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 24.06.2021
- Beginn
- 24.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
1st dose administered to 13 year old patient; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (1st dose administered to 13 year old patient) in a 13-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21a) for COVID-19 vaccination. No Medical History information was reported. On 24-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 24-Jun-2021, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (1st dose administered to 13 year old patient). On 24-Jun-2021, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (1st dose administered to 13 year old patient) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 28.08.2021
- Impfdatum
- 23.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Pharmacist gave the shot after 15 hours that the vial was opened; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Pharmacist gave the shot after 15 hours that the vial was opened) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Jun-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Pharmacist gave the shot after 15 hours that the vial was opened). On 23-Jun-2021, EXPIRED PRODUCT ADMINISTERED (Pharmacist gave the shot after 15 hours that the vial was opened) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- -
- Geschlecht
- U
- Eingang
- 28.08.2021
- Impfdatum
- 24.06.2021
- Beginn
- 24.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Doses administered in pre-drawn syringes left out for over 12 hours at room temperature; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses administered in pre-drawn syringes left out for over 12 hours at room temperature) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 24-Jun-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 24-Jun-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses administered in pre-drawn syringes left out for over 12 hours at room temperature). On 24-Jun-2021, EXPIRED PRODUCT ADMINISTERED (Doses administered in pre-drawn syringes left out for over 12 hours at room temperature) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 24.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
pre-drawn syringes that were withdrawn and left out at room temperature for over 12 hours. At least one to three of the doses were administered to patients.; This spontaneous case was reported by a consumer and describes the occurrence of PRODUCT STORAGE ERROR (pre-drawn syringes that were withdrawn and left out at room temperature for over 12 hours. At least one to three of the doses were administered to patients.) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 24-Jun-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage form. On an unknown date, the patient experienced PRODUCT STORAGE ERROR (pre-drawn syringes that were withdrawn and left out at room temperature for over 12 hours. At least one to three of the doses were administered to patients.). At the time of the report, PRODUCT STORAGE ERROR (pre-drawn syringes that were withdrawn and left out at room temperature for over 12 hours. At least one to three of the doses were administered to patients.) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medication was provided. No Treatment medication was provided. Most recent FOLLOW-UP information incorporated above includes: On 07-Jul-2021: Non Significant Follow-up information was added; Reporter address was added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 24.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
pre-drawn syringes that were withdrawn and left out at room temperature for over 12 hours. At least one to three of the doses were administered to patients.; This spontaneous case was reported by a consumer and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (pre-drawn syringes that were withdrawn and left out at room temperature for over 12 hours. At least one to three of the doses were administered to patients.) in an 18-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 24-Jun-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (pre-drawn syringes that were withdrawn and left out at room temperature for over 12 hours. At least one to three of the doses were administered to patients.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (pre-drawn syringes that were withdrawn and left out at room temperature for over 12 hours. At least one to three of the doses were administered to patients.) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment medications were provided Most recent FOLLOW-UP information incorporated above includes: On 07-Jul-2021: Follow-up information received on 07-jul-2021 contains non significant information as another reporter added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 23.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chromaturia
Dysuria
Pollakiuria
Symptomtext
Little cramping and uncomfortable feeling only when urinating and felt burning at the end of the urination; Little tiny light pink in urine/After 30 minutes when urinate again it has little red; Pee more than the usual and this was just after the vaccine; This spontaneous case was reported by a consumer and describes the occurrence of DYSURIA (Little cramping and uncomfortable feeling only when urinating and felt burning at the end of the urination), CHROMATURIA (Little tiny light pink in urine/After 30 minutes when urinate again it has little red) and POLLAKIURIA (Pee more than the usual and this was just after the vaccine) in a 49-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051c21a) for COVID-19 vaccination. No medical history was provided by the reporter. Concomitant products included AMLODIPINE for an unknown indication. On 23-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Jun-2021, the patient experienced DYSURIA (Little cramping and uncomfortable feeling only when urinating and felt burning at the end of the urination), CHROMATURIA (Little tiny light pink in urine/After 30 minutes when urinate again it has little red) and POLLAKIURIA (Pee more than the usual and this was just after the vaccine). At the time of the report, DYSURIA (Little cramping and uncomfortable feeling only when urinating and felt burning at the end of the urination), CHROMATURIA (Little tiny light pink in urine/After 30 minutes when urinate again it has little red) and POLLAKIURIA (Pee more than the usual and this was just after the vaccine) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. The patient took Tylenol right after the vaacination, for unknown indication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chromaturia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- AMLODIPINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 24.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Pre-drawn syringes that were withdrawn and left out at room temperature for over 12 hours. At least one to three of the doses were administered to patients; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Pre-drawn syringes that were withdrawn and left out at room temperature for over 12 hours. At least one to three of the doses were administered to patients) in an 18-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 24-Jun-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Pre-drawn syringes that were withdrawn and left out at room temperature for over 12 hours. At least one to three of the doses were administered to patients). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Pre-drawn syringes that were withdrawn and left out at room temperature for over 12 hours. At least one to three of the doses were administered to patients) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment medication information was provided. Most recent FOLLOW-UP information incorporated above includes: On 07-Jul-2021: Follow up information received on 07-JUL-2021 contains no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 27.04.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product dose omission issue
Symptomtext
Now past the 42 day mark (around 60 days) and has not yet received the second dose.; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT DOSE OMISSION ISSUE (Now past the 42 day mark (around 60 days) and has not yet received the second dose.) in a 21-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Apr-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PRODUCT DOSE OMISSION ISSUE (Now past the 42 day mark (around 60 days) and has not yet received the second dose.). At the time of the report, PRODUCT DOSE OMISSION ISSUE (Now past the 42 day mark (around 60 days) and has not yet received the second dose.) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication provided by reporter. No treatment medication provided by reporter. Most recent FOLLOW-UP information incorporated above includes: On 12-Aug-2021: Follow-up received included non-significant information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product dose omission issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 22.06.2021
- Beginn
- 22.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Device connection issue
Underdose
Symptomtext
Needle might have leaked out; Believed that she gave 0.3mL or 0.4mL of the dose instead of the full dose; This spontaneous case was reported by a pharmacist and describes the occurrence of DEVICE CONNECTION ISSUE (Needle might have leaked out) and UNDERDOSE (Believed that she gave 0.3mL or 0.4mL of the dose instead of the full dose) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Jun-2021, the patient experienced DEVICE CONNECTION ISSUE (Needle might have leaked out) and UNDERDOSE (Believed that she gave 0.3mL or 0.4mL of the dose instead of the full dose). On 22-Jun-2021, DEVICE CONNECTION ISSUE (Needle might have leaked out) and UNDERDOSE (Believed that she gave 0.3mL or 0.4mL of the dose instead of the full dose) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided. Treatment information was not provided. Reporter did not allow further contact Most recent FOLLOW-UP information incorporated above includes: On 21-Jul-2021: No new information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Device connection issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 27.08.2021
- Impfdatum
- 19.06.2021
- Beginn
- 19.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site discolouration
Symptomtext
pink spot below the injection site after second dose; This spontaneous case was reported by a patient and describes the occurrence of VACCINATION SITE DISCOLOURATION (pink spot below the injection site after second dose) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Jun-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Jun-2021, the patient experienced VACCINATION SITE DISCOLOURATION (pink spot below the injection site after second dose). At the time of the report, VACCINATION SITE DISCOLOURATION (pink spot below the injection site after second dose) outcome was unknown. Not Provided No concomitant medications were reported. No treatment information was provided by the reporter. This case was linked to MOD-2021-230043 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site discolouration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.08.2021
- Impfdatum
- 17.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Accidental exposure to product
Device connection issue
Symptomtext
The needle detached from the syringe and the vaccine spilled out; The needle detached from the syringe and the vaccine spilled out; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL EXPOSURE TO PRODUCT (The needle detached from the syringe and the vaccine spilled out) and DEVICE CONNECTION ISSUE (The needle detached from the syringe and the vaccine spilled out) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Jun-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced ACCIDENTAL EXPOSURE TO PRODUCT (The needle detached from the syringe and the vaccine spilled out) and DEVICE CONNECTION ISSUE (The needle detached from the syringe and the vaccine spilled out). At the time of the report, ACCIDENTAL EXPOSURE TO PRODUCT (The needle detached from the syringe and the vaccine spilled out) and DEVICE CONNECTION ISSUE (The needle detached from the syringe and the vaccine spilled out) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No relevant concomitant medications reported. No treatment information was provided. Pharmacist called to report that when she went to give an injection in a patients left arm on 17Jun21 lot3 051C21A the needle detached from the syringe and the vaccine spilled out. She did not think the patient got very much of the dose if any. She was going to reinject in opposite arm. She gives consent to be contacted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental exposure to product
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 27.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 22.07.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 03.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hour after real punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 23.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 22.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 22.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reactive to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 01.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine was administered 12 hrs after vial was punctured.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 04.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 14.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted Vaccine administered over 12 hrs after vial was punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 29.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse patient reaction noted Vaccine was administered 12 hrs after vial was punctured.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 23.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 13.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction noted to patient Vaccine was administered over 12hrs after vial was punctured.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 30.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 28.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 02.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted Vaccine administered 12 hrs after vial was punctured.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 21.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial puncture
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 22.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hrs after vial was punctured.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 14.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted Vaccine administered over 12 hrs after vial was punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 09.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted Vaccine administered over 12 hrs after vial was punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 22.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 01.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted Vaccine was administered after 12 hrs of vial being punctured.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 21.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 03.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 20.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 22.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N / A
- Aktuelle Erkrankungen
- N / A
- Vorgeschichte
- N / A
- Andere Medikamente
- N / A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 28.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N / A
- Aktuelle Erkrankungen
- N / A
- Vorgeschichte
- N / A
- Andere Medikamente
- N / A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 22.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 21.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong technique in product usage process
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N / A
- Vorgeschichte
- N / A
- Andere Medikamente
- N / A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 28.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
No adverse reaction to patient noted. Vaccine administered over 12 hours after vial punctured.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 10.06.2021
- Beginn
- 11.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Dose administered 24 hours after first puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered 24 hours after first puncture) in a 32-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 11-Jun-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered 24 hours after first puncture). On 11-Jun-2021, EXPIRED PRODUCT ADMINISTERED (Dose administered 24 hours after first puncture) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications were not reported. Treatment details not provided. Pharmacist stated that a vial of Moderna COVID-19 Vaccine was first punctured on 10Jun2021 at around 11 am and got a dose from that vial on 11Jun2021 at around 11 am, more than 12 hours after the first punctured. Pharmacist provided consent for safety team to contact patient on her phone number.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 22.08.2021
- Impfdatum
- 15.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Influenza like illness
Interchange of vaccine products
Symptomtext
Pt received Pfizer Covid vaccine 8-1-21 at another facility. We did not know this at the time we administered the Moderna on 8-15-21 and the patient informed staff that he had never received a Covid vaccine before. This was brought to my attention by an RPh as she checked the database when pt presented to her location on 8-22-21 to receive his second dose of Pfizer vaccine. This thus constitutes the second dose in the series being administered too soon as well as being administered with the wrong brand. (We would not have done this if we had known about the first dose being administered elsewhere). I spoke with the patient 8-22-21 and he stated he had not had any adverse effects other than mild flu-like symptoms. I advised him the series is considered complete now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- unknown
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 20.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
at this time, no adverse events
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none at this time
- Aktuelle Erkrankungen
- Stage 4 bladder cancer.
- Vorgeschichte
- High blood pressure, high cholesterol
- Andere Medikamente
- not known
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 15.08.2021
- Impfdatum
- 01.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dry throat
Throat tightness
Symptomtext
Exactly 15 minutes after having the COVID-19 vaccine made by MODERNA company, I experienced throat closing and became dry. Since then a month has passed and my throat still feels dry.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dry throat
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Sulpha
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 13.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Moderna Covid Vaccine was administered to 12 year old patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 13.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
patient was injected with an expired (past best used date) Moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 12.08.2021
- Impfdatum
- 25.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
There is no adverse reaction or treatment. Didn't realize pt. was under 18. Father wanted his sons to get the vaccination here. We inquired about their age and he stated both were over 18. We didn't catch the dob on application.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 09.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
PT FALSELY REPORTED THAT THEY HAVE NEVER HAD A COVID VACCINE SHOT BEFORE ON THEIR CONSENT FORM AND VERBALLY PRIOR TO RECEIVING THE SHOT. UPON BILLING INSURANCE, IT CAME TO OUR ATTENTION THAT PATIENT HAS ALREADY COMPLETED THE COVID DOSE SERIES IN JANUARY AND FEBRUARY 2021 AT ANOTHER PHARMACY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 09.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Circumstance or information capable of leading to medication error
Extra dose administered
Symptomtext
PT FALSELY REPORTED THAT THEY HAVE NEVER HAD A COVID VACCINE SHOT BEFORE ON THEIR CONSENT FORM AND VERBALLY PRIOR TO RECEIVING THE SHOT. UPON BILLING INSURANCE, IT CAME TO OUR ATTENTION THAT PATIENT HAS ALREADY COMPLETED THE COVID DOSE SERIES IN JANUARY AND FEBRUARY 2021 AT ANOTHER PHARMACY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 07.08.2021
- Impfdatum
- 13.05.2021
- Beginn
- 13.05.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
no adverse event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 04.08.2021
- Impfdatum
- 03.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse reaction reported, however patient is 17 years old and received the Moderna vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 28.07.2021
- Impfdatum
- 26.07.2021
- Beginn
- 26.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Patient received 2nd dose Moderna COVID-19 vaccine on 07/26/2021. During the billing process, insurance reported patient received 1st dose Pfizer COVID-19 vaccine. WAIIS was checked and pharmacy was contacted to confirm 1st dose Pfizer vaccination. Her vaccination card portrayed 1st dose Moderna COVID-19 vaccine. Patient received 1st dose Pfizer from Pharmacy in on 06/10/2021 per RPh (confirmed 7/28/21 via phone) and image of consent form (via fax same day). Patient was contacted and counseled to watch for any unusual symptoms and answered any other concerns patient had.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 23.07.2021
- Impfdatum
- 09.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Underdose
Symptomtext
Syringe only contained about 0.1 ml of vaccine instead of the usual 0.5 ml dose. No one knows how the error occurred. Since the immunizer did not realize the dose was less than expected until the needle was already in the patient's arm, the patient agreed to immediately get another full dose in the opposite arm to ensure a full dose was received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 23.07.2021
- Impfdatum
- 21.07.2021
- Beginn
- 21.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
patient initial request pfizer covid -19 vaccine on consent form, however patient has last minute change due to side effect concern and requested Moderna covid-19 vaccine instead. We missed the age requirement for Moderna covid vaccine and gave the patient Moderna covid 19 vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- I called the patient, and he reported no adverse effect
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 21.07.2021
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19 immunisation
Symptomtext
Patient received his Covid19 Jannsen vaccine April 8, 2021 and came in June 28th, 2021 and insisted on getting the first of the 2 dose series Covid19 Moderna vaccine. The patient pleaded that he needed to protect himself against the Delta variant. Patient received the Moderna vaccine. I was asked to report this to Moderna vaers.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 immunisation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N?A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 21.07.2021
- Impfdatum
- 15.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Administered the vaccine to patient under 18 years old
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 20.07.2021
- Impfdatum
- 15.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient came with her mother and informed us that she wants moderna vaccine for her son who is 12 years old. My technician typed the prescription as a first dose of moderna vaccine. techinformed me that the vaccine is ready to be injected. I gave the moderna vaccine to the patient and realised that and I spoke to the mother about it and the mother said it is approved by moderna for kids 12years and older and she insisted that, that is what she wants . I advise patient that pfizer vaccine is the only vaccine which is now approved for AUE, for now but patients mother said that is what she wants. There was no reported adverse event. I am reporting because modener has not recievev the AUE aproval from FDA. my recomendation is now as use as off label use
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- no adverse event
- Aktuelle Erkrankungen
- not available
- Vorgeschichte
- -
- Andere Medikamente
- Moderna vaccine
- Allergien
- Not available
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 19.07.2021
- Impfdatum
- 28.06.2021
- Beginn
- 07.07.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Menstrual disorder
Polymenorrhoea
Premature ovulation
Symptomtext
I ovulated early (day 11) and my menstrual cycle was only 21 days long. I am actively trying to get pregnant so I have 1+ years worth of cycle history to show that this 21 day cycle, 10 day luteal phase and day 11 ovulation was an abnormal event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstrual disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- Doxycycline
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 19.07.2021
- Impfdatum
- 07.07.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Mucosal inflammation
Stevens-Johnson syndrome
Symptomtext
Severe mucositis/Steven's Johnson Syndrome.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mucosal inflammation
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- Diabetic ketoacidosis
- Vorgeschichte
- Diabetes (type 1)
- Andere Medikamente
- None reported
- Allergien
- Pork products
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 18.07.2021
- Impfdatum
- 09.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Dose given was beyond the use date (BUD) of 8July2021; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose given was beyond the use date (BUD) of 8July2021) in a 35-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose given was beyond the use date (BUD) of 8July2021) (seriousness criterion medically significant). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose given was beyond the use date (BUD) of 8July2021) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant information was provided by the reporter. The pharmacist reported that they had 5 refrigerated vials that went the beyond use date of 08JUL2021. Out of them 1 vial was used for 4 patients on 09JUL2021 and that was beyond the use date. The pharmacist also reported that those vials were refrigerated on 08JUN2021and are not supposed to be given after its BUD of 08JUL2021. The other 4 vials are still sealed, unused and kept for disposal. No treatment information was provided by the reporter. Company comment: This report refers to a case of Expired product administration error for mRNA-1273, with no associated adverse events. This appears to be non-serious, but RA has reported this as a serious event. However, more information is required to determine the serious criteria. Most recent FOLLOW-UP information incorporated above includes: On 09-Jul-2021: Follow-up information received does not contain any new information (NNI); Sender's Comments: This report refers to a case of Expired product administration error for mRNA-1273, with no associated adverse events. This appears to be non-serious, but RA has reported this as a serious event. However, more information is required to determine the serious criteria.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 17.07.2021
- Impfdatum
- 16.07.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
On 7/16/21, patient's mother requesting to get first dose of Moderna vaccine for her child. Intern consulted patient and I supervised the administration of vaccine after briefly reviewing the consent form. I must have overlooked the date of birth and focused on all the questions on form and COVID screening questionnaire. I did not remember the patient but I must have reviewed the form as I signed on it after intern's initials. The error was not caught until the prescription was processed. I immediately contacted mom, and explained the situation. She was not aware that EUA has not approved for age 12 and up. I suggested contacting Dr and monitored the approval status of Moderna vaccine before having patient return for second dose 4 weeks later. Mom said patient has been feeling good after the vaccine. Dr was contacted but will be out of office until 7/21. Mother is notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 16.07.2021
- Impfdatum
- 16.07.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The vial was left in the refrigerator for 31 days. The dose was given on the 31st day, 1 day past expiration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 14.07.2021
- Impfdatum
- 14.07.2021
- Beginn
- 14.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Received 2nd dose on day 120 instead of the recommended by day 42.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 14.07.2021
- Impfdatum
- 10.07.2021
- Beginn
- 14.07.2021
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Device leakage
Symptomtext
PATIENT RECEIVED A VACCINE FROM A PUNCTURED BUT REFRIGERATED VIAL 48 HOURS AFTER 1ST PUNCTURE. NO ADVERSE EVENTS REPORTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Device leakage
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 14.07.2021
- Impfdatum
- 10.07.2021
- Beginn
- 14.07.2021
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
PATIENT RECEIVED A VACCINE FROM A PUNCTURED VIAL THAT HAD BEEN REFRIGERATED FOR 48 HOURS. NO ADVERSE EVENTS HAVE BEEN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 14.07.2021
- Impfdatum
- 10.07.2021
- Beginn
- 14.07.2021
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Device material issue
No adverse event
Product storage error
Symptomtext
PATIENT RECEIVED A VACCINE FROM A VIAL THAT WAS PUNCTURED BUT REFRIGERATED FOR 48 HOURS. AS OF NOW, NO ADVERSE EVENTS REPORTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Device material issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 14.07.2021
- Impfdatum
- 15.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Burning sensation
Swollen tongue
Tongue erythema
Symptomtext
tongue was swallen and redden, burning sensation after drinking alcohol, no problem to eat or dring anything else
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Burning sensation
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 14.07.2021
- Impfdatum
- 14.07.2021
- Beginn
- 14.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
Symptomtext
Pt is 16 yrs old and given Pfizer on 6/16/21 for the first dose and Moderna for the second dose on 7/14/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Seasonal allergies
- Andere Medikamente
- Accutane, flonase, zyrtec
- Allergien
- no allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 12.07.2021
- Impfdatum
- 10.07.2021
- Beginn
- 10.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Pt is 17 years and 11 months old, and was given Moderna shot with is approved for 18 years old and over. Pt has had no symptoms or adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 12.07.2021
- Impfdatum
- 09.07.2021
- Beginn
- 12.07.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Tenderness
Symptomtext
Marble sized lump felt under skin on left size of body where neck and chest meet (lowest part of neck). Painful to touch. Ibuprofen taken - still waiting for lump to disappear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- None performed yet.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- No
- Allergien
- Lactose Intolerance
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 09.07.2021
- Impfdatum
- 06.07.2021
- Beginn
- 08.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Feeling abnormal
Musculoskeletal discomfort
Symptomtext
Pt states shoulder looks/feels like an apple. started late day two. It is now day three.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None
- Andere Medikamente
- Not known
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 09.07.2021
- Impfdatum
- 08.07.2021
- Beginn
- 08.07.2021
- 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
The vaccine that was administered to the patient had passed its beyond use date/time. The vial used had been removed from the refrigerator and punctured at 3:42pm the previous day. The vaccine was administered within 24 hours of the vial being punctured/removed from the refrigerator.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE INDICATED ON FORM
- Vorgeschichte
- NONE INDICATED ON FORM
- Andere Medikamente
- -
- Allergien
- NONE INDICATED ON FORM
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 08.07.2021
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
THIS VACCINE IS APPROVED FOR AGE 18 AND OVER, PATIENT IS 14 YEARS OLD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 08.07.2021
- Impfdatum
- 08.07.2021
- Beginn
- 08.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
WE GAVE THE PATIENT 2ND DOSE TOO EARLY. SHOULD BE 4 WEEKS APART FROM THE FIRST DOSE, BUT WE DID IT 2 WEEKS APART
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ADHD
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 08.07.2021
- Impfdatum
- 08.07.2021
- Beginn
- 08.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
Pt was given first dose of Moderna on June 29,2021 and came back and was administered 2nd dose of Moderna same lot number 051c2a on today. no reaction observed. pt tolerated first vaccine without any reaction or response. will follow up with pt daily. Pt was assessed by FNP and was given Tylenol in the clinic no reaction observed. no fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- htn, gerd
- Vorgeschichte
- none
- Andere Medikamente
- tylenol prn hctz amlodipine estradiol protonix lasix effexor astelin nasal spray
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 08.07.2021
- Impfdatum
- 26.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erectile dysfunction
Panic attack
Symptomtext
Erectile Dysfunction; Panicking; This spontaneous case was reported by a consumer and describes the occurrence of ERECTILE DYSFUNCTION (Erectile Dysfunction) in a 31-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 051C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 26-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Jun-2021, the patient experienced ERECTILE DYSFUNCTION (Erectile Dysfunction) (seriousness criterion medically significant) and PANIC ATTACK (Panicking). At the time of the report, ERECTILE DYSFUNCTION (Erectile Dysfunction) and PANIC ATTACK (Panicking) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medication information was mentioned No treatment medication information was mentioned Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erectile dysfunction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 07.07.2021
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Exposure during pregnancy
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
On 7/7/21, PT came to get a first dose of Moderna Vaccine. (Vaccinator) confirmed that this was her first dose and she never got any other Covid vaccine before. educated PT about the Moderna Covid Vaccine, went over potential ADR and gave her the vaccine. Later that afternoon, (technician) created a batch for the vaccine and got a rejected claim from the insurance. Upon calling the insurance, found out PT got Pfizer vaccine at Walgreens on 5/8/21. The staff pharmacist reached out to the patient but couldn't get a hold of her on 7/6/21 evening. Next morning (today), was able to talk to the patient, and the patient initially claimed that she never got the Pfizer vaccine. She gave her insurance card and signed a consent form at Walgreens but she had to leave for work then called the Walgreens to confirm, but the technician there said she did get a vaccine there. called PT back to call that Walgreens to sort this issue out. And later talking to PT again, she said she then remembered getting Pfizer Vaccine at Walgreens. She apologized for her mistake and said because she is pregnant and has been getting so many different vaccines, she didn't remember getting a Covid vaccine, asked PT to reach out to her doctor immediately and explained that for now, she does not need another dose of Moderna Vaccine based on CDC recommendation (Pt is considered fully vaccinated if 2 different mRNA vaccine is given at least 4 weeks apart).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure during pregnancy
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- Zoloft 50mg Prenatal Vitamins
- Allergien
- No known allergy
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 06.07.2021
- Impfdatum
- 02.07.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Heart rate increased
Symptomtext
Patient stated that 2-3 hours after taking the shot she got a rapid heart rate like her heart was going to beat out her body. Heart rate was 162. Patient stated that she took Aspirin with warm water. Patient stated that she had the same reaction with the flu Vaccine. Patient stated that the rapid heat beat lasted about a day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate increased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- High Blood pressure Lymphdema Heart Murmur May have a small leak in her heart Vale
- Andere Medikamente
- Omacitine
- Allergien
- Penicillin Tylenol Codeine mold Cortozine Sulfer Drugs
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 05.07.2021
- Impfdatum
- 25.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Interchange of vaccine products
No adverse event
Symptomtext
Patient had appointment scheduled at another facility for 21 day interval because it scheduled based on Pfizer, his first dose was moderna, they almost gave him Pfizer. He came here and all our safety check failed and he received the mderna vaccine 21 days from 1st dose. We realized after a few dates the error. Patient was contacted and reported no issue or side effect more than after the first dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 05.07.2021
- Impfdatum
- 21.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vaginal haemorrhage
Symptomtext
After years of being in menopause, I had vaginal bleeding for 7 days, it became very light after 4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaginal haemorrhage
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- Telismartan and Hydrochlorothiazide 80mg Felodipine 5mg
- Allergien
- gluten, coconut, eggs
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 03.07.2021
- Impfdatum
- 16.06.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 16,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Tenderness
Symptomtext
Patient reported lump near collarbone about "3/4 size of a golfball" that only hurts when pushed. Developed on 7/2/21 in the evening
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 03.07.2021
- Impfdatum
- 02.07.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient was administered dose 7 days too early. At the time no symptoms occurred. The CDC was consulted. CDC informed me that patient will not have to be re-vaccinated, that she may experience more severe side effects, and to report to VAERS. The patient was contacted and informed that side effects may be more severe, and there is no need for revaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None Reported
- Andere Medikamente
- None reported
- Allergien
- No known food or drug allergies
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 02.07.2021
- Impfdatum
- 02.07.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Syringe issue
Underdose
Symptomtext
Vaccine leaked out from syringe at time of administration. Proportion leaked out estimated as more than half. Another dose was prepared and given in the opposite (right) arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 02.07.2021
- Impfdatum
- 02.06.2021
- Beginn
- 01.06.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
patient dad registered on line the wrong date of birth on patient. patient born 05/25/2005 and dad did his paper work as 5/25/2002 which qualified him for moderna vaccine. So patient was only 16 when he got moderna vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 02.07.2021
- Impfdatum
- 03.06.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 28,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Off label use
Product administered to patient of inappropriate age
Symptomtext
THERE WERE NO ADVERSE EVENTS. AS STATED BY THE MANUFACTURER, THIS IS AN OFF LABEL USE BECAUSE THE PATIENT IS 15 YEARS OLD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.07.2021
- Impfdatum
- 01.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Interchange of vaccine products
No adverse event
Symptomtext
Patient had received Pfizer series (2 shots) at another location; date unknown to us. Patient claimed that her antibody test showed negative after her second shot so her doctor recommended her to redo the series. She made appointment at our pharmacy for Moderna shot 7/1/21 first dose. On her consent form, she checked NO to question "Have you received a vaccine for COVID in the past". We gave her the shot then billed insurance afterwards. Insurance came back with rejection that patient had Pfizer series. We contacted patient and she confirmed she already had Pfizer series. The case was reported to pharmacy manager and regional supervisor. We were advised to fill out this report for CDC future use. Patient had NO adverse effects but this form had to be filled out so some of the questions would not be relevant regardless of the answers.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Rheumatoid Arthritis
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 01.07.2021
- Impfdatum
- 29.06.2021
- Beginn
- 30.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye swelling
Lymphadenopathy
Symptomtext
Patient called stating lymph nodes were swollen under neck and under arms. Under eye was a little swollen as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 01.07.2021
- Impfdatum
- 30.06.2021
- Beginn
- 30.06.2021
- 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
No adverse event
Symptomtext
After the vaccine was given it was discovered the vaccine was expired past the recommended 12 hour period, at most 31 hours after puncture the dose was given. No adverse reaction was reported and the manufacturer was contacted regarding whether the patient needs to be re-dosed to complete the vaccine series
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High Blood Pressure, High Triglycerides, Depression, High Cholesterol, Family Hx blood clots
- Andere Medikamente
- Labetalol 200mg Twice daily, Zoloft 100mg once daily, Fenofibrate once daily, Aspirin 81mg
- Allergien
- Penicillin - Rash
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 01.07.2021
- Impfdatum
- 30.06.2021
- Beginn
- 30.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
No adverse event
Symptomtext
Patient had previously received Janssen Covid-19 vaccine on 04/06/2021. No current recommendation for booster doses or taking vaccine by additional different manufacturer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- n/a; patient does not report any symtpoms or adverse effects
- Aktuelle Erkrankungen
- no known
- Vorgeschichte
- -
- Andere Medikamente
- unknown
- Allergien
- no known
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 30.06.2021
- Impfdatum
- 24.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Symptomtext
Right cervical Shingles; treated with antiviral meds
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- PE
- Aktuelle Erkrankungen
- denied
- Vorgeschichte
- denied
- Andere Medikamente
- progesterone HRT; Folic acid
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 29.06.2021
- Impfdatum
- 29.06.2021
- Beginn
- 01.06.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
No adverse event
Symptomtext
The patient made an appointment for Moderna Dose#2 vaccination. After giving her the Moderna vaccination, she pulled her card for me to enter the vaccination Information and then I realized she had her first dose with Pfizer manufacturer. We suggested her to stay in place for more than 30 minutes to for observation. However, the patient is completely fine even after 30 minutes of administration of the vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 29.06.2021
- Impfdatum
- 25.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
No adverse event
Symptomtext
Patient was mistakenly given Moderna vaccine as second dose but was actually supposed to receive pfizer as second dose . Patient was fine, no adverse reaction reported and we instructed him not to receive any other doses of the COVID vaccines. He had received a dose of pfizer on 06/04/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- n/a
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 28.06.2021
- Impfdatum
- 24.06.2021
- Beginn
- 24.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
No adverse event
Symptomtext
pt had already completed course of Pfizer in February , his MD had done a blood assay to test for the antigen it came back as negative and his MD recommended he get the moderna vaccine now - no reaction yet but unsure due to different vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- none that I am aware of
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 26.06.2021
- Impfdatum
- 11.06.2021
- Beginn
- 13.06.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast swelling
Lymphadenopathy
Menstrual disorder
Menstruation irregular
Symptomtext
Swollen lymph nodes in upper neck and breasts 15 hours after shot. Breasts nodes still swollen. Neck nodes go up and down. Menstrual cycle 10 days after shot. Prior to both doses, cycle was EXTREMELY irregular. Could go anywhere from 67-139 days between cycles. This was 32 days. Shortest cycle I?ve had.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Effexor xr 350mg Allegra 180mg Omeprazole 20mg
- Allergien
- Nickel
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 25.06.2021
- Impfdatum
- 24.06.2021
- Beginn
- 24.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine injected was in syringe that had been drawn over 12 hours earlier
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 25.06.2021
- Impfdatum
- 24.06.2021
- Beginn
- 24.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine injected was in syringe that had been drawn over 12 hours earlier
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 25.06.2021
- Impfdatum
- 24.06.2021
- Beginn
- 24.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product preparation issue
Symptomtext
Vaccine injected was in syringe that had been drawn over 12 hours earlier
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 23.06.2021
- Impfdatum
- 23.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac flutter
Feeling jittery
Symptomtext
Fluttery heartbeat, jittery Started around 30 minutes after the injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac flutter
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- 150 mg zoloft daily 81 mg aspirin
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 22.06.2021
- Impfdatum
- 21.06.2021
- Beginn
- 21.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Disorientation
Symptomtext
I just want to report that in the evening that I took the Moderna dose #2, I felt disoriented. My wife took my blood pressure. The reading was 88/58 and my pulse was 73. I am wondering if there is an interaction between the vaccine and the high blood pressure medication. I stayed lied down until I fell asleep. In he morning of 6/22/21 from 8:03 AM to 8:06 AM, lying down my readings were 99/65 and pulse 61. Sitting down the readings were 103/67, pulse was 66. Standing the readings were 103/74 and pulse was 80. Oxygen was 97. The last readings at 1:42PM after eating were 126/75 and pulse was 80. I am wondering if there is any correlation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Disorientation
- Hospital-Tage
- -
- Labordaten
- None. I am on PTO. So, I am staying home
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Edarbyclor 40/12.5 mg
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 22.06.2021
- Impfdatum
- 22.06.2021
- Beginn
- 22.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
over 42 days apart 1st dose 04/26/21, 2nd dose 06/22/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 22.06.2021
- Impfdatum
- 22.06.2021
- Beginn
- 22.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
over 42 days apart 1st dose 04/26/21, 2nd dose 06/22/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 21.06.2021
- Impfdatum
- 21.06.2021
- Beginn
- 21.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient's age has not been approved for Moderna yet. No adverse reactions reported 3 hours after vaccination, right before reporting this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 21.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syringe issue
Underdose
Symptomtext
During administration the syringe broke and vaccine leaked out. An unknown amount of vaccine was administered to patient resulting in a sub-therapeutic dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma and pre-diabetic
- Andere Medikamente
- N/A
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 17.06.2021
- Impfdatum
- 17.06.2021
- Beginn
- 17.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Face injury
Fall
Symptomtext
Patient was administered vaccine around 11:15 am. patient was seated for about 10 minutes then when he walked over in front of the pharmacy counter, we heard a sound that appeared to be the sound of someone falling. I along with my technicians walked outside of the pharmacy and found the patient lying face down on the floor and bleeding from a cut on his chin that happened as a result of the fall. patient remained on the floor until EMTs arrived about 10 minutes later
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Face injury
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 17.06.2021
- Impfdatum
- 17.06.2021
- Beginn
- 17.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
Patient was given Moderna vaccine but should have been given Pfizer vaccine based on patient age of 14.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 16.06.2021
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 7+
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Symptomtext
WAITED IN THE STORE FOR 15 MINUTES. THEN GOT READY TO LEAVE. WHILE LEAVING HE FELL DOWN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fall
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -