- Staat
- -
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 20.06.2023
- Impfdatum
- 12.10.2021
- Beginn
- 28.11.2022
- Tage bis Beginn
- 412,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Myocarditis
Obstructive sleep apnoea syndrome
Symptomtext
OBSTRUCTIVE SLEEP APNEA ACUTE NON ST ELEVATION MI MYOCARDITIS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 02.03.2023
- Impfdatum
- 11.10.2021
- Beginn
- 01.08.2022
- Tage bis Beginn
- 294,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Angiogram pulmonary abnormal
COVID-19
Death
General physical health deterioration
Pain
Pneumonia
Positive airway pressure therapy
Pyrexia
SARS-CoV-2 test positive
Therapy cessation
Symptomtext
8/23/22 pt had a positive COVID test at Center; was give Azithromycin and Medrol Pak; 8/27/22 pt brought to ED with fever, body aches, O2 saturation in 80s; O2 supplementation; CTA chest shows multifocal pneumonia; pt's condition worsened; transitioned to DNR, comfort measures; family requested BiPAP to be removed and patient passed away in the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 19,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DM, THYROID DISEASE, FATTY LIVER DISEASE
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 30.12.2022
- Impfdatum
- 11.04.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 203,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Hypoxia
Oxygen saturation decreased
Pneumonia serratia
Respiratory failure
Respiratory rate increased
SARS-CoV-2 test positive
Vomiting
Symptomtext
Patient with history of anoxic brain injury and persistent vegetative state. She was brought to the ED by EMS on 10/31 after she had an episode of emesis and associated drop in sats at her LTCF. When she arrived to the ED, she had increased respiratory rate and hypoxia. Patient tested positive for COVID in the ED by PCR. Ultimately, she was admitted 10/31 - 11/16 for acute on chronic hypoxic respiratory failure, Serratia pneumonia, and COVID pneumonia. She was discharged back to her LTC on 11/16. She has received the primary COVID vaccine series and one booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 06.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 26,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Death
Delirium
Encephalitis
Hypoxia
Interchange of vaccine products
Symptomtext
pt admitted to hospital with delerium secondary to hypoxia, COVID 19 encephalitis; given Decadron, O2 supplementation; admitted to hospice as GIP hospice; dc'd to home with hospice where he passed away; death certificate and med records sent per VAERS request
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, COPD, anxiety, chronic pain, lymphoma, brain stem aterovenous malformation, chronic respiratory failure
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 06.05.2022
- Impfdatum
- 22.10.2021
- Beginn
- 11.01.2022
- Tage bis Beginn
- 81,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray abnormal
Death
Dyspnoea
Electrocardiogram abnormal
Fatigue
Malaise
Myocardial infarction
Pneumonia
Urinary tract infection
Symptomtext
Patient transported to Hospital via ambulance from his home on 3/6/2022 and died at the hospital same day from myocardial infarction. Had not felt well since 1/11/22 when he was seen in clinic at Health Facility by Dr. for UTI, dyspnea, fatigue. Treated for UTI and pneumonia. EKG was done at the time as well as a chest X ray . His wife believes that his death was due to side affects from the Covid-19 vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- EKG, Chest X ray 1/11/22 at Health Facility.
- Aktuelle Erkrankungen
- UTI, Dyspnea, fatigue
- Vorgeschichte
- Seizure disorder , Recurrent UTI, Urinary retention, Pleurisy HX Right leg DVT, dizziness, Neck injury Hx: Knee replacement last year
- Andere Medikamente
- 1/3/22 Ciprofloxacin 500 mg one by mouth BID 1/11/22Dexamethasone 4 mg two by mouth daily X 5 days 1/11/22 Levofloxacin 500 mg one by mouth X 7 days
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 08.10.2021
- Beginn
- 19.02.2022
- Tage bis Beginn
- 134,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute myocardial infarction
COVID-19 pneumonia
Cardiorenal syndrome
Death
Renal impairment
Respiratory disorder
Unresponsive to stimuli
Symptomtext
78 year old female with severe CAD was admitted for Covid-19 pneumonia and NSTEMI. Cardiology signed off with recommendations for NOAC. Her pulmonary status continued to worsen. She became unresponsive and was DNR. Renal function declined and determined to be due to cardiorenal syndrome. She became unresponsive. She passed away this morning at 1055 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 11,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- valvular heart disease, HTN, pacemaker, PAD, carotid stenosis, CAD, CHF, Afib, COPD, kidney disease
- Andere Medikamente
- ASA, Iron, multivitamins, D2, Lipitor, Toprol, Lasix, klor-con, ventolin,
- Allergien
- mag citrate, iodine, adhesive, fentanyl, versed
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 29.01.2022
- Impfdatum
- 19.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Chest pain
Computerised tomogram thorax abnormal
Condition aggravated
Dyspnoea
Feeling abnormal
Pulmonary embolism
Pulmonary thrombosis
Vaccination complication
Symptomtext
I was hospitalized on January 20 with multiple pulmonary emboli in both lungs. I had been feeling poorly for weeks following my booster shot. I started to get short of breath and eventually had significant chest pain. My wife called an ambulance and I was transferred to the hospital where I was treated for the pulmonary emboli. The Emergency Room doctor and the on call Hematologist both diagnosed the blood clots as a result of the mRNA vaccine. Additionally, I had a significant reaction to the second Moderna shot in May 2021. I had a fever of 101.5 and chills and body aches for two days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 2,0
- Labordaten
- The pulmonary emboli was diagnosed with a chest CT scan. I was placed on blood thinners and will have follow on tests to check for any additional complications.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Previous pulmonary embolism
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood culture negative
Culture urine negative
Death
Erythema
Full blood count normal
Hypophagia
Lethargy
Metabolic function test normal
Pain in extremity
Peripheral swelling
Pyrexia
Skin warm
Tachycardia
Urine analysis normal
Symptomtext
Patient received COVID booster shot on 11/9/2021. Within 24 hours patient's left arm became erythematous, warm, swollen, painful. Attending M.D. was notified and ordered course of doxycycline. No other reaction noted until the week beginning on 11/15/2021 the patient began having low grade fevers and was more subdued, quieter. The patient became more lethargic by 11/17/2021 and PO intake declined as a result. Attending M.D. ordered CBC, CMP, blood cultures and urine analysis with C+S on 11/17/21. Labs did not have significant findings. The patient continued to be extremely lethargic, very minimal PO intake, having fevers, tachycardia. Patient deceased on 11/20/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Patient received COVID booster shot on 11/9/2021. Within 24 hours patient's left arm became erythematous, warm, swollen, painful. Attending M.D. was notified and ordered course of doxycycline. No other reaction noted until the week beginning on 11/15/2021 the patient began having low grade fevers and was more subdued, quieter. The patient became more lethargic by 11/17/2021 and PO intake declined as a result. Attending M.D. ordered CBC, CMP, blood cultures and urine analysis with C+S on 11/17/21. Labs did not have significant findings. The patient continued to be extremely lethargic, very minimal PO intake, having fevers, tachycardia. Patient deceased on 11/20/2021.
- Aktuelle Erkrankungen
- No acute illness at time of vaccination or one month prior
- Vorgeschichte
- History of pulmonary embolism, vascular dementia, adjustment disorder with depressed mood, history of TIA and CI, Type II DM, muscle weakness, history of encephalopathy
- Andere Medikamente
- Citalopram 10 mg tablet, Humalog Insulin, Mirtazapine 7.5 mg tablet, Voltaren Gel 1% topical
- Allergien
- Allergic to cayenne pepper
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 27.10.2021
- Beginn
- 21.01.2022
- Tage bis Beginn
- 86,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthroscopy
COVID-19
Cerebral artery occlusion
Cough
Dizziness
Fatigue
Headache
Hypotension
Loss of consciousness
SARS-CoV-2 test positive
Syncope
Unresponsive to stimuli
Symptomtext
Patient is a 50 year old female with PMH of hypothyroid, headache, anxiety/depression, TBI s/p MVA, HTN and recently diagnosed with a cerebral venous occlusion who presents to the ED after a syncopal episode. As per patient, she had a BM, started to leave the bathroom and felt dizzy. Patient sat back down and then when attempting to return to the bedroom she had a syncopal episode without warning. As per the patient, her wife said that she had loss of consciousness for 1-2 minutes. The patient said that her wife said her eyes were open but "no one was home". Patient reports that she had c/o coughing, headache and fatigue and was diagnosed with covid 1/19/22. Patient is double vaccinated with Moderna. Patient denies chest pain, shortness of breath and is no longer coughing. as per ED record, patient was hypotensive enroute to ED and received IV fluids. In the ED, rapid covid test is positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- 1,0
- Labordaten
- 01/20/2022 - SARS-COV-2 Antigen (++)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Depression, HTN, Hypothyroidism; Other Anxiety, Addt'l Med History TBI 2009 due to MVA, occasional memory issues, PTSD, chronic headaches, syncope. Significant Surg Hx As Listed Common C-Section, Cholecystectomy, R TKA; Addt'l Surgical History discectomy, lumber discectomy L4-L5, right knee arthroscopy. Smoking Status Never Smoker.
- Andere Medikamente
- buPROPion HCl 150 mg Tablet Extended Release 24 hr Directions: 1 tablet oral daily every morning (Active) buPROPion HCl 300 mg Tablet Extended Release 24 hr Directions: 1 tablet oral daily every morning (Active) cetirizine (ZyrTEC) 10
- Allergien
- Adhesive tape; bee venom
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose
Loss of consciousness
Seizure
Vomiting
Symptomtext
Patient was getting booster dose of moderna after initially getting J+J as first dose. Patient said he gets nervous around needles, but has not had a seizure before. Dose was given at around 10:05 am. About 1 minute after vaccination patient fell unconscious and started moving head back and forth with eyes opening and closing, his arms were tight i believed it looked like a seizure. It lasted about 10-15 seconds, the patient threw up 3 times after regaining consciousness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- called 911 they checked blood sugar, blood pressure. EMT recommended going to ER but patient refused and had parents drive him home.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anxiety
- Andere Medikamente
- Alprazolam, mirtazapine, venlafaxine, buspirone.
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Seizure
Symptomtext
Patient has a history of seizures. The day after the vaccine she expierenced a seizure, reported to the ER, was treated, and now has no issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Electric shock sensation
Extra dose administered
Headache
Tremor
Symptomtext
Patient presented to doctor's office complaining of headache in the form of electric shock in the left parietal area that lasts for few seconds, pain is severe, symptoms started in the middle of the night Wednesday after having a Covid vaccine booster Wednesday afternoon, happens every few minutes, causes her head and sometimes whole body to shake, tried Tylenol and Motrin with some improvement. Exam unremarkable now, continue Motrin 800 mg 3 times daily with food and follow-up if no improvement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 19.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Seizure
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Seizure-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 16.10.2021
- Beginn
- 16.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Condition aggravated
Dizziness
Loss of consciousness
Symptomtext
Pt started to feel weak and said that he was about to pass out. He got on the floor and felt weak. I asked if he had eaten anything and the wife said no. I quickly gave him some water and told him to sip slowly on it. After a few seconds, he passed out. I asked the wife to move so I could give him an epi-pen and she said no. Both her and her son shouted at him to wake up and slapped his face. He finally came to after a few minutes. I asked the son to go get him so peanut butter crackers. He snacked on it slowly, while sipping on water. He started feeling bad again and laid on his back and we elevated his feet. After ~5-10 minutes, he started feeling better and sat up. After about 30 minutes, he was able to stand and felt better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- Moderna first shot (per wife, he felt like he was going to pass out after he left, but he didn't)
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 12.10.2021
- Impfdatum
- 08.10.2021
- Beginn
- 10.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electric shock sensation
Insomnia
Pruritus
Symptomtext
Sudden onset severe itching of hands and toes , like I was being electrified by stinging insects. It was off and on for a day Severe insomnia now for 2 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zoloft Vitamin d calcium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 03.10.2021
- Impfdatum
- 03.10.2021
- Beginn
- 03.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient fainted within 5 minutes of administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 30.09.2021
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dehydration
Fall
Syncope
Vertigo
Symptomtext
Patient fainted, fell to floor, no injuries, was surprised he was on floor. Stated he had walking vertigo and had no drank any liquid that day. sat patient in chair gave water and he felt much much better. Patient departed on his own after a time, said he was doing fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- "Walking Vertigo" Dehydration
- Vorgeschichte
- "Walking Vertigo"
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Dizziness
Fatigue
Flushing
Hyperhidrosis
Hypotension
Nervousness
Syncope
Tremor
Unresponsive to stimuli
Symptomtext
Systemic: Abdominal Pain-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Exhaustion / Lethargy-Mild, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Mild, Systemic: Hypotension-Mild, Systemic: Shakiness-Severe, Additional Details: Patient recieved Moderna Covid vaccine and was waiting for the 15 mins, friend came over to tell me that he friend was shaking, when I went over to the patient she was unresponsive. After about 15-20 seconds she was reponsive, after further discussion with the patient she said this has happened before when she gave blood, she said she was extremely nervous and thinks that is what caused the reaction BP was 90/60 at first after it was back to normal at 120/80. She did not want to call Emergency.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 25.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Dizziness
Dyspnoea
Fatigue
Flushing
Hyperhidrosis
Nausea
Syncope
Tachycardia
Tremor
Unresponsive to stimuli
Vomiting
Symptomtext
Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Abdominal Pain-Medium, Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Medium, Systemic: Shakiness-Mild, Systemic: Tachycardia-Mild, Systemic: Vomiting-Medium, Additional Details: 5-6 minutes after receiving her Moderna dose (1st dose for patient), she started displaying signs of an allergic reaction. It was not clear if she was in full-blown respiratory distress, but her breathing seemed more labored and she seemed more and more lightheaded, so 1 dose of EpiPen 0.3 mg was administered. Potential respiratory distress immediately improved upon EpiPen being administered, but then the primary symptom became Nausea and Vomiting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 21.09.2021
- Beginn
- 21.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Heart rate increased
Hyperhidrosis
Paraesthesia
Presyncope
Symptomtext
I administered the 2nd dose of Moderna vaccine. 2-3 mins later the boyfriend of patient alerted me that patient felt like passing out. I gave a cold compress. Pt was semi-responsive, diaphoretic, felt dizzy, said her fingers were tingling. She was holding her chest and the boyfriend said her HR was elevated. I called 911 and EMS responded, 45 mins later, the patient was fine and left the store
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- chronic migraines
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 16.09.2021
- Impfdatum
- 16.09.2021
- Beginn
- 16.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Pharyngeal swelling
Syncope
Symptomtext
Patient was faint, light headed, throat swelling, had a history of anaphylaxis, gave epinephrine injection in left thigh, called 911 and ems took her to hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes
- Andere Medikamente
- hydrocodone/acetaminophen
- Allergien
- Keflex contrast
- Vorherige Impfungen
- flu shot last year anaphylaxis
- Staat
- AR
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 07.10.2023
- Impfdatum
- -
- Beginn
- 26.09.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Autoimmune disorder
Condition aggravated
Influenza like illness
Migraine
Stem cell transplant
Therapeutic product ineffective
Symptomtext
Migraine that didn?t respond to any medications (tried all available) but Imitfex but wouldn?t get rid of it only took it from a 10 to a 5. Stem cell IV 3 months later finally resolved it. Also had flu like symptoms for 48 hours and then had an autoimmune response to the vaccine and all my diseases flared for over a month despite increased prednisone. My rheumatologist said all his patients had autoimmune responses to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Rheumatoid Arthritis/Lupus NPSLE, Sjogren?s Syndrome, Raynaud?s Phenomenon, Central Sleep Apnea, Chronic Migraine & Fatigue, Degenerative Disk Disease, med/severe spinal stenosis & herniation L4 & 5, High Cholesterol, Hypoglycemia, Irritable Bladder, Microvascular Angina/INOCA ischemia with no obstructive coronary artery disease, GERD, IBS, Leukopenia, Menopause, Peripheral Neuropathy, Laryngopharyngeal Reflux (LPR), COPD
- Andere Medikamente
- B Complex, Baclofen, C buffered, Zyrtec, Evoxac, Cranberry, Aricept, Adderral, Cymbalta, E, Famvir, Duragesic, Fish Oil, Fluorometholone 0.1% drop, Neurontin, Boniva, Remicade, Arava, Singular, 1-a-day 50+ multivitamin, Nitrofurantoin, Zofr
- Allergien
- Zithromax, Astepro, Beta-blockers, Wellbutrin, Bentyl, Enbrel, Erythromycin, HRT, Linzess, cozar, Minicin, Benicar, Altace, Zoloft, Sulfa Drugs
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 29.09.2023
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Biopsy uterus
Heavy menstrual bleeding
Lethargy
Mobility decreased
Muscular weakness
Myalgia
Polymenorrhoea
Ultrasound pelvis
Symptomtext
Within 20 minutes of shot experienced pain in weakness in right arm and lethargy. Within 4 hours of shot I experience joint/muscle pain and weakness in my entire body from head to my toes. I had so much pain even moving I needed to crawl on my hands and knees to get to the restroom. This continued for between 7 2 and 96 hours AFTER injection. My daughter received her 2nd dose the same time I did and experienced the same symptoms approximately 8 hours after the injection. Approximately October 19, 2021 I began bleeding menstrually (early). I saw the ob-gyn at Medical Center and was referred to OB/GYN Dr. for the first time on Nov 8, 2021 to address the bleeding. She attempted putting me on a different birth control pill to stop the bleeding, which was excessive. I bled through a pack of pads every 2 days through February 2022. On February 7, 2022, Dr performed a pelvic ultrasound and a uterine biopsy trying to determine the cause of the bleeding. My birth control pill was switched again and the bleeding finally got under control by March, 2022. She felt it was in relation to the Covid vaccine I had received. I was advised by her AND my PCM to report it as an adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Pap exam 11/07/2021, pelvic ultrasound and uterine biopsy 02/07/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acid reflux, environmental/seasonal allergies
- Andere Medikamente
- Vitamin D, Vitamin E, Pepcid AC 20mg, Zyrtec, Singulair, Junel BCP, Pataday eye drops
- Allergien
- Penicillin, Ceclor, Paraphenylenediamine (PPD) a chemical in hair dye.
- Vorherige Impfungen
- Flu vaccines, injection site swelling, rash and pain
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 15.03.2023
- Impfdatum
- 30.09.2021
- Beginn
- 17.01.2022
- Tage bis Beginn
- 109,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Cartilage injury
Insomnia
Magnetic resonance imaging
Mobility decreased
Muscle atrophy
Hypoaesthesia
Injected limb mobility decreased
Injection site pain
Nerve injury
Pain
Periarthritis
Rotator cuff syndrome
Symptomtext
On 09/30/2021 I received the first Moderna vaccine in my right shoulder and since receiving that injection I?ve been suffering with nerve damage, chondral injury, rotator tear lesion, adhesive capsulitis, loss of muscle mass and mobility, in constant pain and problems sleeping.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- MRI TEST RESULTS on 07/15/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Muscle relaxers
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 15.03.2023
- Impfdatum
- 30.09.2021
- Beginn
- 17.01.2022
- Tage bis Beginn
- 109,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Cartilage injury
Insomnia
Magnetic resonance imaging
Mobility decreased
Muscle atrophy
Hypoaesthesia
Injected limb mobility decreased
Injection site pain
Nerve injury
Pain
Periarthritis
Rotator cuff syndrome
Symptomtext
On 09/30/2021 I received the first Moderna vaccine in my right shoulder and since receiving that injection I?ve been suffering with nerve damage, chondral injury, rotator tear lesion, adhesive capsulitis, loss of muscle mass and mobility, in constant pain and problems sleeping.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- MRI TEST RESULTS on 07/15/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Muscle relaxers
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 20.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
Blood cortisol
Chronic fatigue syndrome
Computerised tomogram abdomen
Computerised tomogram thorax
Condition aggravated
Echocardiogram
Electrocardiogram
Full blood count
Hypertension
Metabolic function test
Troponin
Ultrasound abdomen
Symptomtext
Two days after vaccine booster developed unexplained paroxysmal surge in hypertension accompanied by new onset atrial fibrillation with rapid ventricular response that lasted 10 hours and self-terminated. Accompanied by chronic fatigue syndrome, which has persisted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 2,0
- Labordaten
- October 28-November 1, 2021: EKG, echocardiogram, CBC, BMP, troponin, CT & abdominal chest, retroperitoneal ultrasound, urine cortisol
- Aktuelle Erkrankungen
- hypertension
- Vorgeschichte
- hypertension
- Andere Medikamente
- Valsartan/HCTZ 80/12.5 mg daily. Aspirin 81 mg daily, Multivitamin daily, Calcium 600 mg daily, Vit D3 2000 IU daily
- Allergien
- IV iodinated contrast
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 27.01.2023
- Impfdatum
- 01.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 11,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Electrocardiogram
Symptomtext
Chest pains in the left side and right side over the past 1.5 years.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- ECG, no results.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 05.08.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 93,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Asymptomatic COVID-19
Hypotension
SARS-CoV-2 test positive
Tachycardia
Symptomtext
from his nursing home with concerns of weakness, hypotension, and tachycardia, also found to COVID-19 positive. He appears to be asymptomatic from this and has been previously vaccinated so we will simply monitor for the time being. Patient had the moderna vaccine on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 27.10.2021
- Beginn
- 23.04.2022
- Tage bis Beginn
- 178,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Dyspnoea
Lethargy
Pneumonia
Pneumonia aspiration
Symptomtext
Hospitalized: 4 days of COVID-19 infection with increased dyspnea and lethargy. Lobar pneumonia probably aspiration not COVID-19 related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 28.09.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 41,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Dyspnoea
Electrocardiogram abnormal
Tachycardia
Symptomtext
Tachycardia, atrial fibrillation, dyspnea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Electrocardiograms
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, GERD, Chronic Kidney Disease
- Andere Medikamente
- Toprol 100mg, Losarten 100mg, Chlorthalidone 25mg, Omeprazole 20mg, Tamsulosin 0.4mg, Simvastatin 10mg, , Testosterone 20.25mg, Calcium 500mg, Zinc, 40mg, ASA 81mg, Fish Oil 800mg, Co-Q10 200mg, Probiotic,
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 05.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dehydration
Pyrexia
Vomiting
Symptomtext
Patient stated that she had to be hospitalized around 12 hours after receiving this vaccine. She stated she had severe dehydration, fevers, vomiting, that required her to go to the emergency room.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown (possible moderna allergy from this event)
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 21.09.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 96,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Angiogram
COVID-19
Chest pain
Dyspnoea
Electrocardiogram normal
Exposure to SARS-CoV-2
Headache
Painful respiration
SARS-CoV-2 test positive
Ultrasound Doppler
Vomiting
Symptomtext
Patient is fully vaccinated. COVID positve on 12/26/2021 at ED visit. 21yo female presents with COVID concern. She reports multiple exposure to COVID including her boyfriend who she lives with. States onset of shortness of breath and chest pain that is worse with inspiration since yesterday. The sharp pain comes and go and has not had pain like this before. She also states that she has a frontal headache which is somewhat similar to her previous headaches. Had 1 episode of vomiting which has now resolved. CTA was negative for PE. U/S duplex was negative for DVTs bilaterally.EKG was negative for acute ischemia.Vitals within normal limits on arrival. No hypoxia or respiratory distress. Pt discharged from ED. Given information for monoclonal antibodies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 01.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Migraine
Tinnitus
Vomiting
Symptomtext
April 1, 2021 I received J&J Vaccine. Nov 1, 2021 I received the Moderna Booster. Days after the booster I now have constant ringing in my ears. I also get headaches regularly most of my adult life. After the Moderna Booster I have had 2 insanely painful migraines that made me dysfunctional for an entire day with vomiting. Never experienced a migraine this intense prior to the Moderna booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- I have an appointment with my Primary Care Physician on 1/31/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- LUTERA (28) 0.1/20 TAB
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 16.01.2022
- Impfdatum
- 03.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Electrocardiogram normal
Inflammation
Tinnitus
Symptomtext
12/4/2021, I woke to chest pains. 12/5/2021, I woke to ringing in the ears. Tinnitus on 12/6/2021. I called the doctor to report symptoms and ask when they felt they would subside. They brought me in that afternoon and did an exam and EKG. The EKG showed normal. But there was inflammation in the chest area. I was told the symptoms "should" subside, but they both continue to this day. The doctor suggested continuing to take my Advil PM at night to help with the inflammation, which I have done. The chest pain is constant but fluctuates at times stronger and then less. On a scale of 1-10, it was a 2 with spikes of 3 and is now a 1 with spikes of 2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Low-dose Aspirin, Multivitamin, Vitamin C 1000mg, Cal 750mg, Norethindrone
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 24.09.2021
- Beginn
- 01.09.2011
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adhesion
Blood test normal
Mobility decreased
Nerve compression
Symptomtext
Woke up and could not turn head, arm, and shoulder. On the next day scheduled an appointment and saw the doctor 2 days later. Blood test and physical. Not sure what had caused issue but referred to physical therapist. There it was determined that I had a kind of pinched nerve but therapist diagnosed it as a stuck facia. Physical therapy and tools to help exercise to help it. After 6 weeks still working on recovery.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Only physical except for blood test(normal)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HBP
- Andere Medikamente
- Triamterene/HCTZ, Quinapril, Atorvastatin, Allopurinol, Terbinafine, Acetaminophen
- Allergien
- Penicillin and all derivatives
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Amylase increased
Carbon dioxide increased
Chills
Dyspnoea
Influenza like illness
Myalgia
Pyrexia
Symptomtext
After the Johnson and Johnson after 30 minutes it felt like I swallowed a golf ball. I have mass cell activation syndrome and I was asked to take the Moderna, I anticipated some reaction. By the end of the day I had chills and 101 fever, muscle aches and flu like symptoms. This lasted for about a week. The second week I felt off I went back to see my allergist doctor, about two weeks later. I had shortness of breath and they let me know I had something in my chest and they gave me an antibiotics and steroid pills 10mgs that lasted 5 days and 10 day Keflex due to my autoimmune I normally feel feverish and it amplifies anything else i might have. I felt I could've gotten sick. I saw my PCP and they did some blood work.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None at the time of the doctor visit. They just did an exam. I saw my PCP and they did some blood work Amylase levels was elevated. carbon dioxide levels in blood were elevated. On my visit on Nov 30th. This will be compared with my Allergist , and I'm waiting on that.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mass cell activation Syndrome Asthma and my allergens . Esophageal motility disorder and high blood pressure. Optic neuritis Chronic Pancreatitis hypoglycemia Arthritis and increased CPK levels, It could be suggested that Polymyositis myositis I might have a mild case of MS Kidney stones. and chronic UTI's
- Andere Medikamente
- I was told to take 10mgs of prednisone and 25 mgs of Benadryl Sodium Cromolyn 100 mgs 3x a day Zyrtec 10 mgs twice a day Pepcid 10mgs in the morning and 20mgs in the evening Labetalol 100mgs twice a day Wellbutrin once a day , it's 1
- Allergien
- I can only take two kinds of antibiotics. I'm allergic to everything else Keflex 250mgs dose and I take Clindamycin, I can only take the pediatric dose of about 75mgs/5mls I usually take it about 3x a day. For food I have a shellfish allergen tree grass mold, and cats make me allergic I'm have an allergen to Iodine contrast and latex.
- Vorherige Impfungen
- after the Johnson and Johnson first vaccine after 30 minutes it felt like I swallowed a golf ball
- Staat
- NC
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- 20.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Fatigue
Postmenopausal haemorrhage
Symptomtext
Post menopausal 2+ years, yet a few days after the 2nd COVID shot, I had a period for over 7 days. Not 'spotting'; it required tampons with multiple changes throughout the day. Also experienced shortness of breath for two weeks and fatigue lasting 5-6 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Topical Steroid Withdrawal
- Andere Medikamente
- Progesterone 200mg, Estradial .75 patch, Low Dose Naltrexone HCL 6mg
- Allergien
- Food preservatives
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 09.11.2021
- Impfdatum
- 16.09.2021
- Beginn
- 17.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose increased
Blood ketone body increased
Condition aggravated
Diabetes mellitus
Diabetes mellitus inadequate control
Pain
Pyrexia
Symptomtext
So, ever since my first dose of the covid vaccine, my body doesn't process sugars as effectively as it used to. I have had to adjust my insulin dosaging as well as my insulin tolerance levels. Before the vaccine, I would give 1 unit of fast acting insulin for every 10 carbs. through out the day. In the morning when I would wake up I would give 1 unit of insulin every 9.5 carbohydrates. After the vaccine, the 2nd dose made the symptoms worse. I now give 1 unit of insulin for every 9 carbohydrates for my first meal. For the "lunch" i give 1 unit of insulin for every 10 carbohydrates. and for the evening, after about 11 hours of being awake, I have to give 1 unit of insulin per 7.8 carbohydrates. When I sleep. My insulin basically becomes non-active and I often wake up with high glucose levels. My daily dose of toujeo remained at 23 units 1x a day. Below is the adverse events I had in more detail. The first week was just like the 2nd week, but the 2nd week was worse. This was taken from my social media page where I thought to catalogue the events. For the first 7 days I had moderate to large ketone levels. This Will Update Regularly until the 10/28 Disclaimer: This is not medical advice just my observation and the steps that I took after receiving the Moderna Vaccine. If you or anyone you know has type 1 #diabetes and gets the #Moderna vaccine. Ensure they are vigilant with their glucose levels, #ketone levels, and food. I got the first dose about 2 weeks ago, and I've had trace amount of ketones on a regular basis. At least 6 days out of the 14 days. Prior to the vaccine, I would only have ketones 1x or 2x a year. My A1c last checked was 6.1 (a couple weeks prior to 1st dose of vaccine), and 6.5 prior to that. Edit: I want to add that my lifestyle hasn't changed in anyway prior to or after the first dose of vaccine that would've caused me to have higher occurrences of ketones. Update 1: after 14 days my #ketoneLevels were back to normal, meaning negative every time. UPDATE 2nd Dose #Moderna Received 10/14/2021 After 12 hours, I now have #ModerateKetone levels. Day 2: I experienced a fever of ~100f, and body ached. When I woke up this morning. I think the fever is out of my system. My body doesn't hurt as much. I woke up with my glucose levels @ 63. When I went to the restroom to check my ketone levels it showed trace amounts despite my low glucose levels which is really unusual. For lunch I ate out at restaurant. Within 10 minutes of finishing my meal I checked again. My ketone levels were moderate. Confirms my suspicions that I'll likely be on a jello diet for the next 14 days. Even food with "0 sugar, but had Sugar Alcohols" caused my ketones to increase. Confirmed, not all sugar free products will help eliminate Ketone levels. Today, I will eat mostly jello and other foods that has 0 sugar and I will ensure that there isn't any sugar alcohols. I'll update again once I test it. Day 3: I no long have a fever or body aches. My fever also never got higher than 100.2 on Day 2. I'm still having issues with producing ketones with nearly everything I ate. I tried drinking #powerade but it did not eliminate the ketones. #gatorade is the clear choice for me as it always helps to quickly eliminate any ketones that are produced. Even just eating a measly 11g carbohydrates caused trace amount of ketones. Day 4: I started to eat only pistachios and jello. I'll occasionally have to eat something with a bit more carbs to raise my sugar, but when I do it causes some ketones to appear. Hopefully in 10 days everything will be back to normal. By the end of the day, trace amounts of ketones still appeared. I did some research and it's possible ketones developed even though my glucose stayed around 110 all day due to lack of appropriate caloric intake. Went from over 2000 to less than 1000. Day 5: Woke up to small amount of ketones. Glucose dropped so I ate something to raise my glucose to 146. I had Moderate levels of ketones. After drinking at least 24 oz of water per hour. The ketones still did not get flushed out. I got really hungry and said "Screw It" decided to eat 50 carbs and gave a large enough insulin injection for it. Larger than normal since ketones reduce insulin effectiveness. After about an hour, I checked my ketone levels again. First check was trace amounts, the Second check was negative. Makes me curious. I can only assume this happened because even though I had consumed less carbohydrates the day before, I never had to give an insulin injection other than my Toujeo. Thus ketones developed from lack of insulin even though I didn't necessarily need an injection for the food I consumed on Day 4. Further experimentation/observation is needed. Day 6: Woke up with glucose of 76. The ketone strips wasn't quite negative and it wasn't quite trace amount either. Since I had potentially a trace amount of ketones, I gave a tiny larger injection than I normally would and then I ate some cereal, my typical breakfast, and I checked again. My ketones were now at small. This is an improvement, as the first couple of days no matter what I ate it would've been moderate ketone levels. I started to eat regular meals like I did before covid. My ketones didn't reach about small amounts. Day 7: Woke up with no ketones this morning. This is the first morning since I've taken the moderna vaccine that I've had no ketones. I've continued to eat my meals like I regularly had prior to the vaccine. Larger dosage of insulin was no longer necessary. Seems like this may be the turning point of the complications I've had. At one point I had trace ketones due to a in irregular glucose spike, but no other issues. Day 8 to 13: No ketones. Having to adjust my dosage per 10 carbohydrates on injection until I find a sweet spot again. Sugar is currently running slightly higher than it would be prior to the vaccine. Day 14: Basically everything has resumed back to normal now. Though I have to give a slightly larger dose for meals than I had to prior to the vaccine shot. Hopefully in the coming days everything will return back to normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Type 1 Diabetes since I was 12
- Andere Medikamente
- Toujeo Humalog Inpen
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 09.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest discomfort
Cough
Dyspnoea
Wheezing
Symptomtext
I had persistent chest tightness and cough; and difficulty breathing. Starting on the 1st and was seen on the 3rd at Urgent Care. Wheezing, they noticed that I was doing that when they checked me. They prescribed me with prednisone and Albuterol inhaling to open me up. They also provided an antibiotic in case it was bacterial. They have helped with my symptoms. I'm on the tail end of it, but I do feel better than last week. Note: I had the flu vaccine on the same day, don't know for sure what brand it was.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure Kidney Event - a month after the first day of the COVID-19 vaccine on March 2021 Hypertension
- Andere Medikamente
- Lisinopril 10mg Metoprolol 50mg Twice a Day Amlodipine 10mg Once a Day Crestor 10mg
- Allergien
- N/A
- Vorherige Impfungen
- COVID-19 vaccine dose 2 3- 29-2021. A month after the vaccine, I had an acute kidney injury and I was on dialysis for about a we
- Staat
- -
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 09.11.2021
- Impfdatum
- 05.08.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 93,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Asymptomatic COVID-19
Hypotension
SARS-CoV-2 test positive
Tachycardia
Symptomtext
from his nursing home with concerns of weakness, hypotension, and tachycardia, also found to COVID-19 positive. He appears to be asymptomatic from this and has been previously vaccinated so we will simply monitor for the time being. Patient had the moderna vaccine on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
COVID-19
Dyspnoea
Fatigue
Pneumonia
Weight decreased
Wheezing
Symptomtext
Patient developed Shortness of breath, fatigue, weight loss, loss of sense of smell, wheezing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Patient was admitted to the hospital 11/4/21 and was diagnosed with pneumonia and COVID19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Asthenia
Condition aggravated
Dyspepsia
Fatigue
Neutrophil percentage decreased
Symptomtext
Per the individual. He recevied the booster of Janssen at the pharmacy on 10/25/21. Approximately two days later he had lab work completed at the local office. He was weak and fatiqued. He has also been having a work up due to indigestion and "stomach pain". He stated his Neutrophil level dropped from the "normal range to 42.9 which is a low level in just two days from my booster shot." Advised individual to follow up with PCP for another blood level if necessary
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- See above
- Aktuelle Erkrankungen
- fatigue, stomach pain, indigestion.
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 08.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
Decreased appetite
Dizziness
Hypertension
Myalgia
Nausea
Pain in extremity
Palpitations
Peripheral swelling
Symptomtext
still feeling dizzy; lack of appetite; swollen arm,my arm swollen up pretty much; sore arm; Muscle ache; nausea; heart raising,my heart raising really up; blood pressure up; This spontaneous case was reported by a consumer and describes the occurrence of PALPITATIONS (heart raising,my heart raising really up), HYPERTENSION (blood pressure up), DIZZINESS (still feeling dizzy), DECREASED APPETITE (lack of appetite) and PERIPHERAL SWELLING (swollen arm,my arm swollen up pretty much) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Allergy (Allergic to everything) and Anxiety. Concomitant products included AZELAIC ACID for Acne. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Oct-2021, the patient experienced PALPITATIONS (heart raising,my heart raising really up) and HYPERTENSION (blood pressure up). On an unknown date, the patient experienced DIZZINESS (still feeling dizzy), DECREASED APPETITE (lack of appetite), PERIPHERAL SWELLING (swollen arm,my arm swollen up pretty much), PAIN IN EXTREMITY (sore arm), MYALGIA (Muscle ache) and NAUSEA (nausea). The patient was treated with DIAZEPAM ongoing since an unknown date for Anxiety, at a dose of half pill twice. At the time of the report, PALPITATIONS (heart raising,my heart raising really up) and HYPERTENSION (blood pressure up) had not resolved and DIZZINESS (still feeling dizzy), DECREASED APPETITE (lack of appetite), PERIPHERAL SWELLING (swollen arm,my arm swollen up pretty much), PAIN IN EXTREMITY (sore arm), MYALGIA (Muscle ache) and NAUSEA (nausea) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 28-Oct-2021, Blood pressure measurement: high (High) High. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medicine included Tersac and patient is on blood pressure pills. The patient had an appointment in November to get some cardiac test. Included cardiac lab values (ECG, cardiac test, cardiac enzymes) This case was linked to MOD-2021-370575 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211028; Test Name: Blood pressure; Result Unstructured Data: High
- Aktuelle Erkrankungen
- Allergy (Allergic to everything); Anxiety
- Vorgeschichte
- -
- Andere Medikamente
- AZELAIC ACID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 22.10.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Alanine aminotransferase normal
Blood alkaline phosphatase
Blood magnesium
Blood test
Brain natriuretic peptide
Cardiac stress test
Chest X-ray
Differential white blood cell count
Echocardiogram
Electrocardiogram
Full blood count
Metabolic function test
Mobility decreased
Musculoskeletal chest pain
Pain
Troponin
Symptomtext
Chest tenderness (left side) progressing to stabbing pain. Unable to lie down. This happened over a 3-4 day period.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- 10/29/2021: ECG -Lead Troponin CBC & Differential BNP Basic Metabolic Profile ALT/SGPT Alkaline Phosphatase XR Chest Echocardiogram Stress Test Blood Test - Magnesium
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Condition aggravated
Hypertension
Pain
Palpitations
Pyrexia
Symptomtext
Patient stated she had "normal" side effects from the booster vaccine (aches, pain, fever) about 24 hours after her dose on 10/30. On 10/31 at 3am she awoke with a racing heart. This went away. On Monday, 11/1 the symptoms came back and her rate was racing and she had a blood pressure of 238/118, She went to the ER for full evaluation where she was told they could not find what was wrong and why her blood pressure as so high. The patient is still experiencing high blood pressure (184/78) but is being monitored at home by Dr. . Dr. is working with patient to adjust her dose and suggested that these blood pressure issues "may" be associated from her vaccine dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypothyroidism, High Blood Pressure
- Andere Medikamente
- Bystolic 5mg, Synthroid 75mcg, Vitamin C, Vitamin D, Omega-3 Fish Oil, Vitamin B12
- Allergien
- Penicillin and Bactrim
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Immediate post-injection reaction
Influenza like illness
Ophthalmic migraine
Ophthalmological examination
Pain
Photophobia
Visual impairment
Symptomtext
I had little lines going across going my vision - zig zag. I noticed the lights were really bothering me. My sight - I couldn't see the microwave time very well; couldn't see well. I never have had migraines, but I wondered if it was a migraine coming on. It lasted about 20 minutes and then I could see again. Everything seemed fine to me. Went to the eye doctor and he put something in my eye - he called it a numbing thing; I think....it wasn't an eye dilator. He called it an Ophthalmic Migraine. He said people can have those periodically and so I'll wait and see if I have any more before having a follow up. Right after the vaccine: Achy, head hurt, chills in the night (flu like symptoms) - had this for about a day - within 24 hours, those went away mostly. Note: Flu shot on 9/30/2021 - not sure of the brand name.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ophthalmic migraine
- Hospital-Tage
- -
- Labordaten
- Put something in my eye - to examine eye.
- Aktuelle Erkrankungen
- Norovirus - about a month or so ago - September 19 (stomach bug)
- Vorgeschichte
- Calcified calcium - cardiovascular disease Neuropathy in my feet but I don't take anything for it Insomnia Off and on I have GERD but it's usually under control
- Andere Medikamente
- Ramipril Zetia Rosuvastatin Doxepin Vitamins - Multiple Vitamin - ONE A DAY for 55-year-old + Glucosamine Chondroitin Hydrocele eye tablets with omega 3 AZO Urinary bladder Probiotic Alpha lipoic acid Fluticasone Vaginal cream Melatonin CoQ
- Allergien
- Penicillin Motrin Cipro
- Vorherige Impfungen
- Moderna 2nd dose - flu like symptoms for a day after.
- Staat
- CT
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 27.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Paraesthesia
Symptomtext
Numbing and tingling right foot toes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 02.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dyspnoea
Feeling abnormal
Headache
Herpes zoster
Hyperhidrosis
Hypoaesthesia
Injection site pain
Joint swelling
Lymph node pain
Malaise
Nausea
Painful respiration
Peripheral coldness
Rash
Visual impairment
Symptomtext
Woke up with pillow sweat for the first days; A bad rash/Rash is getting worst; Rash is painful; Lymph node sore; Shingles; Rash under arm/ Then it got worst; Feeling very sick/he has been sick for 24 days since getting first dose; Pain when took a deep breath; Right hand was numb; Middle finger got really cold; Right elbow swollen; Knee swollen; Waves of nausea; Injection site was pretty sore/still lot of arm pain, feel where the injection was; Hard breathing; Vision started going down; No energy/Still no energy; Felt very bad; A headache/still having headache; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (Felt very bad), DYSPNOEA (Hard breathing), VISUAL IMPAIRMENT (Vision started going down), ASTHENIA (No energy/Still no energy) and JOINT SWELLING (Right elbow swollen) in a 66-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Rheumatoid arthritis, Arthritis and Gout, unspecified (Gout problems.). Concomitant products included ACETYLSALICYLIC ACID (BABY ASPIRIN) and PREDNISONE for an unknown indication. On 01-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Oct-2021, the patient experienced FEELING ABNORMAL (Felt very bad) and HEADACHE (A headache/still having headache). On 03-Oct-2021, the patient experienced DYSPNOEA (Hard breathing), VISUAL IMPAIRMENT (Vision started going down) and ASTHENIA (No energy/Still no energy). On 04-Oct-2021, the patient experienced JOINT SWELLING (Right elbow swollen), JOINT SWELLING (Knee swollen), NAUSEA (Waves of nausea) and INJECTION SITE PAIN (Injection site was pretty sore/still lot of arm pain, feel where the injection was). On 05-Oct-2021, the patient experienced HYPOAESTHESIA (Right hand was numb) and PERIPHERAL COLDNESS (Middle finger got really cold). On 09-Oct-2021, the patient experienced PAINFUL RESPIRATION (Pain when took a deep breath). On 11-Oct-2021, the patient experienced MALAISE (Feeling very sick/he has been sick for 24 days since getting first dose). On 13-Oct-2021, the patient experienced RASH (Rash under arm/ Then it got worst). On 15-Oct-2021, the patient experienced HERPES ZOSTER (Shingles). On an unknown date, the patient experienced HYPERHIDROSIS (Woke up with pillow sweat for the first days), RASH (A bad rash/Rash is getting worst), RASH (Rash is painful) and LYMPH NODE PAIN (Lymph node sore). At the time of the report, FEELING ABNORMAL (Felt very bad), DYSPNOEA (Hard breathing), VISUAL IMPAIRMENT (Vision started going down), JOINT SWELLING (Right elbow swollen), JOINT SWELLING (Knee swollen), HYPOAESTHESIA (Right hand was numb), PERIPHERAL COLDNESS (Middle finger got really cold), PAINFUL RESPIRATION (Pain when took a deep breath), HERPES ZOSTER (Shingles), HYPERHIDROSIS (Woke up with pillow sweat for the first days), RASH (Rash is painful), RASH (Rash under arm/ Then it got worst) and LYMPH NODE PAIN (Lymph node sore) outcome was unknown and ASTHENIA (No energy/Still no energy), MALAISE (Feeling very sick/he has been sick for 24 days since getting first dose), RASH (A bad rash/Rash is getting worst), HEADACHE (A headache/still having headache), NAUSEA (Waves of nausea) and INJECTION SITE PAIN (Injection site was pretty sore/still lot of arm pain, feel where the injection was) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No treatment medication were provided. 9-Oct-2021 - Patient experienced nausea 10-Oct-2021- Patient still had a little bit of nausea On 11-Oct-2021 the patient also experienced a spot on his back which he thought that he had a bug bite. Most recent FOLLOW-UP information incorporated above includes: On 22-Oct-2021: Reporter email ID updated, Current condition added, Outcome of event Feeling sick updated from unknown to Not recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Arthritis; Gout, unspecified (Gout problems.); Rheumatoid arthritis
- Vorgeschichte
- -
- Andere Medikamente
- BABY ASPIRIN; PREDNISONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 25.10.2021
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Dizziness
Hypoaesthesia
Mobility decreased
Nervousness
Panic attack
Symptomtext
pt was forced to get vaccine due to work. Pt was very nervous about the vaccine. stated she was forced and didnt want to get the vaccine. pt said she had to get vaccine. After the vaccine was administered pt was in the waiting area due to her allergy she needed to wait 30 min. She got up and came to the drop off window stating she was dizzy and wanted to lay down. We got a mat, pillow and blanket for her. Offered her water and juice. She had no itchy throat. She said she had a heaviness in her chest and her left arm was numb. She could move her left arm and felt my touch when I was helping her. She didnt want me to take her blood pressure. She said she wanted us to call 911 and call her husband. I believe she was having a panic attack. I asked her if she had experienced one before and she said probably. we call 911
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- pt wanted to go to the er
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- pt states none
- Allergien
- sulfa
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 24.10.2021
- Impfdatum
- 15.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Headache
Palpitations
Visual impairment
Symptomtext
Patient has palpitations at 11pm on 10/15/21. She then had visual disturbances at 5:09 pm on 10/17/21 and a headache two hours later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 15.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood pressure increased
Chills
Dizziness
Flushing
Heart rate increased
Hyperhidrosis
Immediate post-injection reaction
Nausea
Nervousness
Tachycardia
Tremor
Symptomtext
Systemic: Chills-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Nausea-Medium, Systemic: Shakiness-Medium, Systemic: Tachycardia-Medium, Additional Details: pt reports that he was very nervous coming in to get the shot and felt immediately lightheaded after administration. we gave him a sugary drink and 2 benadryl and called ems. Patient declined EMS offer to go to the er. They determined his blood pressure and heart rate were slightly elevated but within allowable range. He went home under the care of his partner. I instructed them to report to the er if any other symptoms occur and to follow up with us if there is anything else
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 15.10.2021
- Impfdatum
- 08.10.2021
- Beginn
- 09.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bradycardia
Chest pain
Chills
Dyspnoea
Headache
Pain
Palpitations
Pyrexia
Symptomtext
bradycardia, agonal breathing, chest pain, palpitations, fever, headache, chills, body aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- iv fluids, ekg monitoring, tylenol
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma
- Andere Medikamente
- tylenol otc
- Allergien
- pcn, bees
- Vorherige Impfungen
- palpitations, bradycardia, headache, fever, body aches and chills
- Staat
- NE
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 14.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 02.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Condition aggravated
Discomfort
Dyspnoea
Fatigue
Head discomfort
Headache
Hypoaesthesia
Malaise
Muscle fatigue
Musculoskeletal stiffness
Pain
Pain in extremity
Pallor
Peripheral coldness
Rash
Sluggishness
Symptomtext
He received his vaccine, had arm pain the first day and felt fine. He was in the produce department and his hand started getting cold and white. He does have Raynaud's disease and has a heart condition and was worried that it may be affecting that. It has occurred a few times but has not happened that often, and this was about 1 1/2 hours after the vaccine. With the heart related conditions about noon on Saturday he had taken a few quick steps and his vision started going dark on both eyes, had labored breathing. He checked his temp and everything was fine, 97.4. He rested for a while and felt better, but he was sluggish all day, had fatigue. He went to the CDC website and had a lot of the symptoms listed. He had headache, some fatigue, malaise and arthralgia. He did not feel well, he has low energy but as the day went on he ate something and felt better, but the headache stayed with him, pressure type in nature/numbness. The more activity he did the worse it got. After Tuesday the headache started coming and going. Yesterday he started developing a rash on his back and on the left side of his chest/side and looks similar to shingles, but has no open sore or discharge. He does not have real pain but does have discomfort. He was feeling that the myocarditis was affecting his heart. He saw pictures on the website and the pictures are similar to what he has and also has muscle fatigue/stiffness and soreness. He has discomfort due to the symptoms. He has not called his doctor regarding these symptoms. He had his wellness check but was not able to address his issues he's have due to time restraints. He did have aortic stenosis and surgery for that in the past, 7/23/2019 and now has a pacemaker. He does have a history of toxoplasmosis and it looks like shingles. He has had a Reclast infusion, but has had reactions to that of uncomfortable. He had the 2nd a year later and then a 3rd dose a year after that, felt like he had been hit by a truck, multiple symptoms, but he tuft it out. His Rheumatologist told him that he gets a fracture that he would be on medicine for the rest of his year. His mother was in the hospital for a while after giving birth to him, and he was in the hospital as well after birth and had rheumatic fever as a child.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Arthritis, gout, back pain (3 surgeries), multiple surgeries, A-fib, toxoplasmosis.
- Andere Medikamente
- Uloric and Prednisone.
- Allergien
- Celebrex and Vioxx.
- Vorherige Impfungen
- Two pneumonia vaccines and had symptoms, not severe, but had a lot of fatigue 10-12 hours later, but did feel warm and lethargic
- Staat
- SC
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 09.10.2021
- Beginn
- 09.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Bundle branch block left
Chest discomfort
Chest pain
Feeling hot
Headache
Hypoaesthesia
Injection site erythema
Injection site pain
Injection site swelling
Pain
Paraesthesia
Peripheral swelling
Pyrexia
Tachycardia
Tremor
Symptomtext
Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Body Aches Generalized-Severe, Systemic: Chest Tightness / Heaviness / Pain-Severe, Systemic: Fever-Medium, Systemic: Headache-Severe, Systemic: Joint Pain-Severe, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Shakiness-Medium, Systemic: Tachycardia-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: Partial Left Bundle Branch Blockage. Swelling of extremeties, chest pain, hot spots on legs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Decreased appetite
Dyspnoea
Fatigue
Injection site pain
Insomnia
Lethargy
Pyrexia
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Chills-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fever-Severe, Systemic: loss of appetite-Severe, Systemic: Unable to Sleep-Severe, Additional Details: patient upset about side effect stated her employer required her to receive covid vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 07.10.2021
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Fatigue
Headache
Nausea
Symptomtext
The first shot on 09/02/2021 Lot number 058E21A - I Had no side effects, The second shot number 061E21A on 09/30/2021, Headache started 30 minutes after injection, Headaches continues thru today 10/07/2021 along with nausea and tiredness. I did have chest pain on the second thru fifth day 10/01/2021 thru 10/05/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Tramadol Tylenol Meloxicam Metaxalone
- Allergien
- Medication Allergies: Levaquin, Leflunomide, Omnicef
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 07.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Hypertension
Hyperventilation
Tachycardia
Tremor
Symptomtext
Systemic: shortness of breath-Severe, Systemic: Hypertension-Severe, Systemic: Hyperventilation-Severe, Systemic: Shakiness-Severe, Systemic: Tachycardia-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 07.10.2021
- Impfdatum
- 20.09.2021
- Beginn
- 21.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dyspnoea
Fatigue
Headache
Wheezing
Symptomtext
tightness in chest-very difficult to breath- very bad wheezing in chest-extreme tiredness-extreme headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- I had 3 shot in my bottom-a breathing treatment and was given an inhaler
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Paraesthesia
Paraesthesia oral
Symptomtext
Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: Patient experienced mild tingling on her tongue about 30 minutes after vaccine administration. There was no swelling. She was given one tablet of diphenhydramine 25mg and her conditioned improved 10 to 15 minutes later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 06.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Paraesthesia
Sensory disturbance
Symptomtext
Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: patient states "arm feels weird" kind of numb"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 02.10.2021
- Impfdatum
- 22.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
Cold sweat
Dizziness
Dyspnoea
Feeling abnormal
Hyperhidrosis
Palpitations
Vomiting
Symptomtext
clammy; threw up; shortness of breath/cannot catch her breath; dizzy/spinning; rapid heart beat/palpitation; dripping sweat; felt close to pass out.; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (shortness of breath/cannot catch her breath), DIZZINESS (dizzy/spinning), PALPITATIONS (rapid heart beat/palpitation), HYPERHIDROSIS (dripping sweat) and FEELING ABNORMAL (felt close to pass out.) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Co-suspect products included non-company products INFLUENZA VACCINE (FLU VACCINE VII) for an unknown indication and PNEUMOCOCCAL VACCINE POLYSACCH 23V (PNEUMOVAX) for an unknown indication. Concurrent medical conditions included Hypertension (High blood pressure since last one year). Concomitant products included HYDROCHLOROTHIAZIDE, LISINOPRIL (LISINOPRIL/HYDROCHLOROTHIAZIDE) for Hypertension. On 22-Sep-2021, the patient received dose of INFLUENZA VACCINE (FLU VACCINE VII) (unknown route) at an unspecified dose and dose of PNEUMOCOCCAL VACCINE POLYSACCH 23V (PNEUMOVAX) (unknown route) at an unspecified dose. On 22-Sep-2021 at 5:30 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Sep-2021 at 10:30 PM, the patient experienced DYSPNOEA (shortness of breath/cannot catch her breath), DIZZINESS (dizzy/spinning), PALPITATIONS (rapid heart beat/palpitation), HYPERHIDROSIS (dripping sweat) and FEELING ABNORMAL (felt close to pass out.). On 23-Sep-2021, the patient experienced COLD SWEAT (clammy) and VOMITING (threw up). At the time of the report, DYSPNOEA (shortness of breath/cannot catch her breath), DIZZINESS (dizzy/spinning), PALPITATIONS (rapid heart beat/palpitation), HYPERHIDROSIS (dripping sweat), FEELING ABNORMAL (felt close to pass out.), COLD SWEAT (clammy) and VOMITING (threw up) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood pressure measurement: 72/56 (Low) Blood pressure was 72/56. 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. Treatment medication was not provided by the reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood pressure; Result Unstructured Data: Blood pressure was 72/56
- Aktuelle Erkrankungen
- Hypertension (High blood pressure since last one year)
- Vorgeschichte
- -
- Andere Medikamente
- LISINOPRIL/HYDROCHLOROTHIAZIDE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 30.09.2021
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypertension
Hypoaesthesia
Paraesthesia
Tachycardia
Symptomtext
Paresthesia, numbness, tingling from top of right shoulder extending down to right 5 fingers. Htn, Tachycardia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 30.09.2021
- Impfdatum
- 26.09.2021
- Beginn
- 26.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Arthralgia
Asthenia
Burning sensation
Chest discomfort
Chest pain
Chills
Fatigue
Hypoaesthesia
Injection site bruising
Injection site erythema
Injection site pain
Injection site rash
Injection site swelling
Lethargy
Lymphadenopathy
Nausea
Pain
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Severe, Systemic: Allergic: Rash Generalized-Severe, Systemic: Abdominal Pain-Medium, Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Chills-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Joint Pain-Medium, Systemic: Lymph Node Swelling-Medium, Systemic: Nausea-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extemities)-Severe, Systemic: Weakness-Medium, Additional Details: Patient came in pharmacy on 09/29/21 around 9am and shared with pharmacist he experienced severed bilateral arm pain, enlarged rash localized to arm site where vaccine was administered, neurologic pain , burning/ tingling of extermities, inflammation/swollen lymph nodes, and pericarditis symptoms. pharmacist instructed him to contact dr and share symptoms and adverse reaction to moderna vaccine given on sunday. He shared he would and would follow up. patient stated better feelin
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 29.09.2021
- Impfdatum
- 23.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fatigue
Flank pain
Hypoaesthesia
Loss of personal independence in daily activities
Muscular weakness
Musculoskeletal chest pain
Paraesthesia
Photophobia
Sedation
Tremor
Vision blurred
Visual impairment
Symptomtext
Dizziness, numbness/tingling in both arms and hands for 1 week after injection, severe changes in vision (blurriness/sensitivity to light) for 1 week after injection, extreme muscle weakness for about 5 days after injection to the point of visible shaking when trying to stand/walk up stairs at home. Severe fatigue/sedation to the extent of not being able to stay awake to feed self for 4-5 days after injection, pain in L ribs/flank for about 1 week after injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- None, virtual visit with PCP on 9/23/21.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma- not requiring medications/monitoring.
- Andere Medikamente
- Nuvaring, Phentermine HCL 37.5mg, multivitamin.
- Allergien
- Zest soap, Irish spring soap, Neo/Poly/Dex antibiotic eye drops.
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 20.09.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Arrhythmia
Arthralgia
Back pain
Dizziness
Fatigue
Headache
Heart rate increased
Hypoaesthesia
Laboratory test
Musculoskeletal discomfort
Pain in extremity
Peripheral swelling
Pruritus
Pyrexia
Symptomtext
I started with extreme abdominal pain, back pain, fever, dizziness, fatigue, hip pain. I also felt like I had needles in my back. I had a headache as well. All of this started about 12 hours after the vaccine. I also had a sore arm, itchy and swollen. I did go to the emergency room due to numbness in my right hand and the left side of my face. I also was experiencing fast heart rate. As of today, I am lightheaded, and my heart will get out of rhythm. I am also having numbness in my right hand. My fatigue seems like it is getting better. I am currently waiting for test results to come back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Allergy Pills Hormone Pill Vitamins Tylenol Phentermine Anti-inflammatory Medication Prebiotic Probiotic
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 24.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose decreased
Dizziness
Dry mouth
Feeling hot
Paraesthesia oral
Symptomtext
Patient complained of dry mouth, lips tingling, being hot/light headed. Patient mentioned it could be low blood sugar. She had her mother pick her up and take her to get lunch. We offered her a cold water since she was complaining of dry mouth and being hot after confirming there was no tightness of the throat and no difficulty breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- macrobid allergy - hives
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 23.09.2021
- Impfdatum
- 22.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
Dyspnoea
Hyperhidrosis
Hypoaesthesia
Pain
Pain in extremity
Symptomtext
Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Body Aches Generalized-Medium, Systemic: Pain in lower back and legs difficulty breathing at first but went away before I could administer epipen-Medium, Systemic: Flushed / Sweating-Severe, Systemic: Joint Pain-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: Pt stated she felt like she couldn't breath so I ran out to her and she said she felt like her face was numb. While getting the epipen, I told her to take deep breaths. She said her breathing was fine so I did not administer Epinephrine, she then stated her lower back was hurting and her legs were hurting and she needed to stand up. I checked her vitals, temp was 97.3 and BP was 131/93 pulse 99. Pt followed up with MD and is ok per phone call
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 20.09.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Chest pain
Chills
Cold sweat
Dizziness
Dyspnoea
Hypertension
Hyperventilation
Nasopharyngitis
Tachycardia
Tremor
Symptomtext
Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Hypertension-Mild, Systemic: Hyperventilation-Mild, Systemic: Shakiness-Mild, Systemic: Tachycardia-Mild, Additional Details: COLD, CLAMMY SKIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 07.09.2021
- Impfdatum
- 20.08.2021
- Beginn
- 22.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac flutter
Chest X-ray
Chest discomfort
Chest pain
Electrocardiogram
Full blood count
Metabolic function test
Myocardial necrosis marker
Symptomtext
Chest pain - felt like heart was rubbing against ribs Chest flutters and heaviness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG, CBC, BMET, Cardiac enzymes, Chest X-ray
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 10.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
C-reactive protein increased
Polymyalgia rheumatica
Red blood cell sedimentation rate increased
Synovitis
Symptomtext
pMr symptoms, synovitis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Polymyalgia rheumatica
- Hospital-Tage
- -
- Labordaten
- Elevated sedrate and crp
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, cad, hyperlioidemia
- Andere Medikamente
- Asa , benacar , coreg , Crestor
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 22.09.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Decreased appetite
Influenza
Lethargy
Nausea
Pyrexia
Somnolence
Symptomtext
sleepy/ just wanted to sleep most of the time but it was not that bad; lethargic; loss of appetite; flu; nausea; fever; This spontaneous case was reported by a consumer and describes the occurrence of SOMNOLENCE (sleepy/ just wanted to sleep most of the time but it was not that bad), LETHARGY (lethargic), DECREASED APPETITE (loss of appetite), INFLUENZA (flu) and NAUSEA (nausea) in an adult female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 061E21A and 037F21A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Previously administered products included for Product used for unknown indication: flu vaccine. Past adverse reactions to the above products included No adverse event with flu vaccine. On 22-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Oct-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 SOMNOLENCE (sleepy/ just wanted to sleep most of the time but it was not that bad), LETHARGY (lethargic), DECREASED APPETITE (loss of appetite), INFLUENZA (flu), NAUSEA (nausea) and PYREXIA (fever). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, SOMNOLENCE (sleepy/ just wanted to sleep most of the time but it was not that bad), LETHARGY (lethargic), DECREASED APPETITE (loss of appetite), INFLUENZA (flu), NAUSEA (nausea) and PYREXIA (fever) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No information on concomitant medication were reported. patient received other vaccines in the 4 weeks prior to COVID-19 vaccine. Patient was asking if she will die from getting the Moderna Covid-19 vaccine. She had friends and friends of friends who died ad were dying after getting the vaccine. She was scared that she will also die. She wanted to know what the long-term effects of the vaccine are. She was forced to take the vaccine. After the 1st dose, she felt very sleepy and lethargic. She just wanted to sleep most of the time, but it was not that bad. This lasted for 2 days. After the 2nd dose, she had nausea, fever, was lethargic and had loss of appetite. She felt like she had a bad case of flu, and it was intense. This lasted for 3 days, and she had to take Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 09.11.2022
- Impfdatum
- 23.01.2021
- Beginn
- 10.09.2022
- Tage bis Beginn
- 595,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dizziness
SARS-CoV-2 test positive
Symptomtext
09/10/22 presents to ED for "dizziness" PMHx of "HTN, hyperlipidemia, ischemic CMP, CAD/CABG"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- 09/10/22 SARS-CoV-2 (COVID-19) detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 22.10.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 58,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aortic valve incompetence
COVID-19
Cough
Echocardiogram abnormal
Fatigue
Inferior vena cava dilatation
Insomnia
Left atrial dilatation
Left ventricular end-diastolic pressure increased
Lethargy
Mitral valve incompetence
Nausea
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
Right ventricular systolic pressure increased
SARS-CoV-2 test positive
Symptomtext
The first symptom was coughing. The second symptom was a sore throat. The third was lethargy, fever, and extreme tiredness. I also had congestion and nausea. I had body aches. The cough was persistent, and I couldn't sleep because of it. The symptoms lasted a full seven days. I received monoclonal antibodies. I also received benzonatate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 12/21/2021 covid-19 test positive; 03/21/2022 echocardiogram elevated LVEDP, left atrium mildly dilated, trace amounts of aortic regurgitation, trace to mild amounts mitral regurgitation, trace amounts of tricuspid regurgitation, right ventricular systolic pressure 30.68 mmhg, inferior vena cava mildly dilated, cardiac valvular motion and morphology no evidence of endocarditis, myocarditis, pericarditis, and or PE.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 Diabetes, Hypertension; Hypercalcemia
- Andere Medikamente
- Metformin; atorvastatin; losartan
- Allergien
- Ampicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 31.08.2022
- Impfdatum
- 03.10.2021
- Beginn
- 25.08.2022
- Tage bis Beginn
- 326,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Abdominal pain
Chills
Nausea
Vomiting
Symptomtext
chills, abdominal pain, nausea, vomiting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 29.08.2022
- Impfdatum
- 10.10.2021
- Beginn
- 22.08.2022
- Tage bis Beginn
- 316,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Cough
Fatigue
Symptomtext
activity change, fatigue, cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 96,0
- Geschlecht
- F
- Eingang
- 09.08.2022
- Impfdatum
- 25.10.2021
- Beginn
- 02.08.2022
- Tage bis Beginn
- 281,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Bacteraemia
Blood culture positive
COVID-19
Culture urine positive
Escherichia test positive
Hypoxia
Pyrexia
SARS-CoV-2 test positive
Sepsis
Symptomtext
Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 8/2/2022 Discharge Date: 08/08/2022 PRESENTING PROBLEM: COVID-19 [U07.1] HOSPITAL COURSE: 96-year-old female admitted to Hospital with weakness and fever. In the emergency room she was found to be COVID positive. Additionally she was hypoxemic and was given remdesivir as well as started on oral dexamethasone. Her blood and urine cultures also ultimately grew E coli. She was started on IV Rocephin and given positive blood cultures repeat cultures were done which were no growth at discharge. She was transition from oral Rocephin to orally Cipro prior to discharge to complete 14 days of antibiotic for her bacteremia. She otherwise noted to have significant weakness and was seen by PT and OT on a regular basis with steady improvement. Given her general weakness does felt having her move to assisted living would be beneficial and arrangements were made for her to transition to assisted living. She has a history of fairly frequent bladder infections and was started on vitamin-C 500 mg twice daily in an attempt to reduce the frequency of her bladder infections. At discharge she had 3 days left of oral dexamethasone to complete and was given prescription for this. She otherwise seem to do remarkably well despite her COVID and sepsis diagnosis. Given that she is moving to the Atrium her family requested that she be followed there by Health Geriatrics and home health. Arrangements were made for home health PT OT to follow the patient post discharge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- History of stroke - right cerebellar Seizure disorder (HCC) Hypercholesteremia GERD (gastroesophageal reflux disease) AK (actinic keratosis) Lumbar spinal stenosis Urge incontinence Hard of hearing Age-related osteoporosis without current pathological fracture Nonrheumatic aortic valve stenosis Mitral annular calcification
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet ascorbic acid (VITAMIN C) 500 MG tablet aspirin 325 MG tablet atorvastatin (LIPITOR) 40 MG tablet Calcium Carbonate-Vitamin D (CALCIUM + D) 600-200 MG-UNIT TABS ciprofloxacin (CIPRO) 500 MG tablet
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Chills
Fatigue
Headache
Pyrexia
Tinnitus
Symptomtext
Chills, fever, headache, fatigue, on-going tinnitus
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- hearing test
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- heart condition celiac
- Andere Medikamente
- Immodium AD daily vitamin vitamin D Calcium Vitamin B
- Allergien
- Gluten, penicillin
- Vorherige Impfungen
- Covid Moderna
- Staat
- FL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 30.12.2021
- Beginn
- 24.02.2022
- Tage bis Beginn
- 56,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint swelling
Urticaria
Symptomtext
I started having random hives on my torso, arms, hands and feet that started on 2/24. It has progressed to joints that at times causes severe swelling. I have taken some antihistamine and Benadryl which helped at first but no longer does anything to alleviate the issue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None at this time. Have an appointment with an allergist on 4/5/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Multivitamin Omeprazole Glucosamine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 03.03.2022
- Impfdatum
- 26.10.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Rash morbilliform
Skin lesion
Therapy change
Symptomtext
Pt developed rash approx 1 week after vaccine. Pt had also started new, higher dose of Amlodipine at the same time he got Moderna Booster. Rash started at both ankles and eventually moved up to include whole body. Pt, at the advice of his MD, stopped all mediations. No medications for 1 month but rash persisted and continued to develop new lesions. Before and during this period pt had no new topical products and no new foods. Rash mildly responsive to Prednisone 40mg daily or higher. Not responsive below 40mg. Pt using hydroxyzine to control itch. While rash is getter better, new lesions continue to appear today 3/3/22. Identified as Morbilliform Eruption.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension and Hyperlipidemia.
- Andere Medikamente
- Lisinopril 10mg once a day, Amlodipine 5mg once a day, Atorvastatin 20mg once a day, HCTZ 12.5 mg once a day
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 25.10.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Eye pruritus
Eye swelling
Pruritus
Rash
Urticaria
Symptomtext
11 days after my booster shot, I developed a rash on my arms, chest, and scalp. Treated with Benadryl. On November 5th my eyes started to swell shut and itch severely so I presented to urgent care. Received oral prednisone course and treated with Benadryl. Swelling subsided however full body hives continued. Was administered prednisone shots in my arm which appeared to help for several days but hives returned. Hives are not localized and appear all over body. This report is being submitted on 2/16/22 while I am still experiencing full body hives and itchiness all over body. Benadryl has helped with treating itchiness however is only temporary. Best relief has been by taking 50mg Famotidine HCL every evening before bed. After 3 months of famotidine, the hives still present after running out of medication. We have been under assumption that something in my environment (exposure to dirty boxes @ a charity event) was causing the allergic reaction. As more extensive cases of uticaria following mRNA boosters have been reported, it is becoming a larger known issue which matches my symptoms and timeline. I am not anti-vax, I?m glad I got my three doses and am protected from COVID. I just need help finding out how to cure these hives and get my life back to normal. I cannot keep treating with Benadryl and being in a constant state of drowsiness or hives. Please help me!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- No lab results. Only given two shots of steroids in my arm and prescribed the following medications + OTC Benadryl to treat. Prednisone 50mg oral tablets (11/5/21) Hydroxyzine HCL 50mg (11/17/21-2/7/22) Famotidine 40mg (11/17/21 - 2/7/22)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 05.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Blood test
Chills
Hepatic lesion
Herpes simplex
Herpes simplex test
Injection site pain
Pyrexia
Symptomtext
Started 12 hrs. after vaccine, slight fever of 99-100 and chills, sore arm at injection site, lasted only 12 hours. Then on day 7 erupted with HERPATIC LESIONS / BLISTERS all over buttocks and still having off and on outbreaks constantly of HSV2, I have never had herpes outbreaks in 54 years of my LIFE!!!!! I have been in constant herpes outbreaks since 11/10/21 after the 3rd vaccine and it is now mid Feb. 2022!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- HSV 2 serology unequivocal, decades ago, on blood serology test.
- Aktuelle Erkrankungen
- HX of fibromyalgia for 13 yrs. (chronic widespread muscular-skeletal pain), hypothyroidism
- Vorgeschichte
- Fibromyalgia 13 yrs, hypothyroidism
- Andere Medikamente
- Synthroid, Prozac, Apple cider vinegar pills, glutathione, vitamin B6 and vitamin B12 , melatonin
- Allergien
- Macrodantin
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 21.10.2021
- Beginn
- 11.01.2022
- Tage bis Beginn
- 82,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Headache
Myalgia
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case after vaccination. Tested positive for COVID 1/11/2022. C/O cough, fever, muscle aches, and headache, onset 01/11/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- SARS CoV2 Antigen Positive on 01/11/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None Reported
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 21.10.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 78,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest discomfort
Cough
Fatigue
Headache
Infection
SARS-CoV-2 test positive
Symptomtext
Breakthrough case after vaccination. Tested positive for COVID on 01/11/2022. C/O cough, chest congestion, headache, and fatigue, onset 1/7/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- SARS CoV2 Antigen Positive on 01/11/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes, Lupus, 10yrs post endometrial cancer
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Chest X-ray
Headache
Influenza virus test negative
Malaise
Neck pain
Pyrexia
SARS-CoV-2 test negative
Urine analysis
Symptomtext
Fever 100 by 9pm, 102 by Midnight, which progressed to 105 by 4AM. ER visit malaise, back & neck pain, and headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Covid, Flu, Urinalysis, chest X-ray all negative.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Lymphadenapathy, large rash, swelling after small pox,
- Staat
- NC
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 06.10.2021
- Beginn
- 07.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Acne
Alopecia
Biopsy
Blister
Burning sensation
Erythema
Pruritus
Skin ulcer
Swelling
Symptomtext
PT NOTICED A RED BUMP ON HER BACK THAT WAS INFLAMMED AND HAD A PIMPLE IN THE MIDDLE AND SMALLER ONES IN THE PATCH AREA. IT SPREAD ALL OVER HER BODY, LESIONS ON HER HEAD, BLISTER LIKE PLACES ALL OVER BODY. ITCHES REALLY BAD. IT BURNS BUT DOESNT HURT. HER HAIR HAS GOTTEN THIN AND HAS LOST HAIR. HANDS PEELED OFF AND CAN'T HOLD ANY OBJECTS. HEELS ARE CRACKED OPEN. SKIN IS MOLTING OFF OF HER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- DR DID BIOPSY ON CHEST AREA IN NOVEMBER AND WAS NEGATIVE FOR ANY MALIGNANCIES.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HIGH BLOOD PRESSURE
- Andere Medikamente
- LOSARTAN, SYNTHROID, SINGULAIR, CLONIDINE, TRAZADONE, VIT D3, MAGNESIUM, STOOL SOFTENERS, VIT B6, VIT B12, COQ10, CALCIUM, GLUCOSAMIN CHONDROITIN MSM,
- Allergien
- SEASONAL ALLERGIES
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 05.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Influenza like illness
Lymphadenitis
Pain
Tenderness
Symptomtext
24 hours later I had inflamed lymph node on right armpit, tenderness, extending down the left inner arm several inches and remain approximately 1 week, fatigue and general achiness, flu like symptoms that lasted a few days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- CGRP injection; Synthroid; Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 31.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Renal pain
SARS-CoV-2 test
Symptomtext
Extreme kidney pain. Left kidney. I do have a cyst in kidney and I have passed kidney stones in past. I?m experience covid symptoms waiting for results. Pain In left kidney again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Renal pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- No
- Andere Medikamente
- Vit D3
- Allergien
- Ibuprofen, penicillin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 24.11.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 21,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Mechanical urticaria
Pruritus
Urticaria
Symptomtext
Sudden onset of systemic itchy skin with raised wheals and dermatographia after scratching. Raised wheals and redness subsides approximately one hour after scratching, but systemic itchiness persists and wheals and dermatographia symptoms return after scratching again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- None yet; doctor appointment planned for end of year or early 2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Prescriptions: Finasteride (1mg per day); Dietary supplements: Berberine (400mg per day); Cholecalciferol (1250 mcg per week)
- Allergien
- Sulfa antibiotics
- Vorherige Impfungen
- large rash on left arm after last two Moderna Covid-19 vaccinations administered on 3/18/21 and 4/15/21.
- Staat
- MO
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 21.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Headache
Inflammation
Pyrexia
Rash pruritic
Urticaria
Symptomtext
I had 24 hours later, headache, fever, chills for 24 hrs. I was fine. The rashes started on 31Oct2021, I thought it was bug bites and it was itchy. I woke up and it was fine. 1Nov2021 and the rash turned into hives. I called the doctor as it progressed everywhere and even on my scalp - for a week. Got antihistamine and steroid and 70per cent better and got more antihistamine, rash the has changed and now if I touch my skin its red, inflamed and itchy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma
- Andere Medikamente
- No
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 05.12.2021
- Impfdatum
- 27.11.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Axillary pain
Fatigue
Headache
Lethargy
Symptomtext
Daughter called the pharmacy to report symptoms her mother told her about. Patient reported to daughter that starting 11/27/21 (day of injection) she felt very tired/lethargic, was anxious, and had a headache. As of 11/29/21 she was starting to feel better. She also reported to her daughter on 11/29/21 that her arm under her armpit hurt. Daughter did state patient was starting to feel better, and that she believed the symptoms to be normal response to a vaccine and not of significant concern though she did want to let us know.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Vision blurred
Visual impairment
Symptomtext
Site: Pain at Injection Site-Medium, Systemic: blurred vision-Severe, Systemic: Visual Changes/Disturbances-Severe, Additional Details: pt states that she experienced blurred vision 40 minutes after her 1st dose and it lastes for 10 minutes. she stes that she could not see anything in front of her and had to sit and wait it out. later on that day she experienced it again and it has been re-occuring everyu day since. she will follow up with her doctor today 11/29/21. she states that she did not have any prtoblems with her vision and did not have to wear corrective glasses, but now she has to wear readers(2.0)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 22.10.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 29,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Oropharyngeal pain
Sinus congestion
Symptomtext
Sinus congestion with initial sore throat with cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Thyroid High blood pressure
- Andere Medikamente
- Synthroid Citalopram Meloxicam Ibuprofen Vitamin B-12 Losartan Cholesterol med
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 21.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
Site: Pain at Injection Site-Medium, Additional Details: Patient states that her local site injection reaction of a sore arm is still lingering (11/27/21). Proper landmarks of immunization administration were performed and patient had zero complications upon administration of the vaccine. There is no ecchymosis, red streaking, welt or swelling of the extremity. Denies systemic effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 28.11.2021
- Impfdatum
- 24.10.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 10,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gastrointestinal disorder
Rash
Rash erythematous
Sensation of foreign body
Symptomtext
Red patched on head, face, torso, hands mostly. they are hot and red and if I scratch them at all, they raise up and get much more itchy. Also have strange GERD symptoms intermittently. Like I swallowed something and it is sitting in my lower esophagus stretching. Symptoms continue to persist. They are less frequent. I am currently on day 5 of a medrol dose pack.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- htn
- Andere Medikamente
- Nifedipine ER, baby ASA
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 21.11.2021
- Impfdatum
- 18.10.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye swelling
Lip swelling
Pyrexia
Symptomtext
Had feverish response for 24 hours, then 36 hours later woke up with eyes and lips swollen. Is allergic to ibuprofen but did not take any nor any other medications to alleviate pain symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Ibuprofen
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 21.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Headache
Nausea
Symptomtext
constant headache and intermittent nausea, beginning 3 days after the vaccine and continuing for 1 week
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- Spironolactone
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 09.10.2021
- Beginn
- 10.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Pyrexia
Somnambulism
Symptomtext
Began feeling general fatigue a few hours after second dosage. Approximately 12hrs after dosage I had a fever ranging between 102-104 that lasted for 2.5days. My baseline body temperature runs 94-96. I?ve also noticed 3 separate occurrences of sleep walking after the second dosage. I?ve never had a sleep walking issue ever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypercholestrol
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fall
Fatigue
Feeling abnormal
Joint injury
Limb injury
Pain
Tenderness
Symptomtext
Within 2 hrs after the shot, it was sore and the next day, my arm was very sore and no other symptoms. 2.30PM I went very tired and took 3 hr nap. Achy and tired and brain fog until 9.30PM. Then slept the whole night. 21Oct I was back to normal except for the arm soreness. The arm soreness after a week it was still sore and tender. Currently when I lay on my arm, it's still tender or sore. During the injection, she took it very slowly and injected it into my arm very slowly. Went to doctor for, I fell and hurt my wrist and hand on the right arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Factor Five Leiden
- Andere Medikamente
- No
- Allergien
- Tetracycline
- Vorherige Impfungen
- Tdap when I was pregnant and had flu like symptoms in 2015
- Staat
- -
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Lymphadenopathy
Myalgia
Nausea
Pyrexia
Vaccination site pain
Vomiting
Symptomtext
Headache; Nausea; Vomiting; Low grade fever; Fatigue; muscle ache; Swollen lymph node near the injection site (armpit); general pain at site of injection site; This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (Headache), NAUSEA (Nausea), VOMITING (Vomiting), PYREXIA (Low grade fever) and FATIGUE (Fatigue) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. 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 HEADACHE (Headache), NAUSEA (Nausea), VOMITING (Vomiting), PYREXIA (Low grade fever), FATIGUE (Fatigue), MYALGIA (muscle ache), LYMPHADENOPATHY (Swollen lymph node near the injection site (armpit)) and VACCINATION SITE PAIN (general pain at site of injection site). At the time of the report, HEADACHE (Headache), NAUSEA (Nausea), VOMITING (Vomiting), PYREXIA (Low grade fever), FATIGUE (Fatigue), MYALGIA (muscle ache), LYMPHADENOPATHY (Swollen lymph node near the injection site (armpit)) and VACCINATION SITE PAIN (general pain at site of injection site) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown.No concomitant products were reported.No treatment drugs were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chills
Headache
Pyrexia
Vomiting
Symptomtext
other side of back is pain; Chills; Fever; threw up two times; Headache; This spontaneous case was reported by a consumer and describes the occurrence of BACK PAIN (other side of back is pain), CHILLS (Chills), PYREXIA (Fever), VOMITING (threw up two times) and HEADACHE (Headache) in a 40-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 049C21A and 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Nov-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 BACK PAIN (other side of back is pain), CHILLS (Chills), PYREXIA (Fever), VOMITING (threw up two times) and HEADACHE (Headache). At the time of the report, BACK PAIN (other side of back is pain), CHILLS (Chills), PYREXIA (Fever), VOMITING (threw up two times) and HEADACHE (Headache) was resolving. No concomitant medications were provided by the reporter. No treatment medications were provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 23.09.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 33,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling abnormal
Headache
Inner ear disorder
Malaise
Nausea
Vomiting
Symptomtext
Starting Tuesday, I felt blah and headachy and that lasted through the week. Saturday, 30th, I had vomiting, nausea, light headedness and dizziness- started 01:30 pm and lasted through the night. The next day, I still didn't feel well. Wednesday, the doctor's office called me to follow up. I had constant headaches and I went in, and my ears (inner) were filled with fluid. Saturday, I took Meclizine that I had. They prescribed more Meclizine, Zofran and nasal spray. Since this past Sunday, I have been doing good. I don't have the headaches now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lung Condition
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 07.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pancreatic Neuroendrocrine Tumors
- Andere Medikamente
- Lanreotide, Creon, Bupropion HCl, Dicyclomine, Tamsulosin, Ferrocite, multi-vitamin, Vit. B6, B12, D3, Claritin, Chlortabs, Trazodone, Oxycodone HCl
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 06.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Myalgia
Pyrexia
Symptomtext
Initial onset - Chills, Fever 102 degrees, Muscle Aches Treated with Tylenol, symptoms diminished over the next 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Rosuvastatin Calcium, Losartan Potassium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 24.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast pain
Muscle spasms
Postmenopausal haemorrhage
Ultrasound scan normal
Symptomtext
It started out as spotting on Thursday night, and Friday morning it was bleeding. And that got heavier into Friday and Saturday and then Sunday and Monday it got lighter. And then the bleeding stopped Wednesday or Thursday of this week. By Thursday it was completely gone. I haven't had a period in 3 years due to menopause. I had a tiny bit of cramping, and my breasts were a little sore, so it was kind of like having a period, but those symptoms were not that bad.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast pain
- Hospital-Tage
- -
- Labordaten
- 11/2/2021 Internal ultrasound normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Ulcerative colitis High blood pressure History of liver transplant
- Andere Medikamente
- Tacrolimus famotidine metoprolol Stelara injection every 2 months, hadn't had an injection in a month
- Allergien
- Contrast dye from CAT scans
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pruritus
Pruritus
Symptomtext
patient had itching at injection site, and itching on face starting 10 minutes after injection. itching lasted for several hours even after a dose of 25mg of benadryl was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Lymphadenopathy
Myalgia
Oral herpes
Pyrexia
Symptomtext
103.7?F Fever on the 30th, still having mild fevers. Been treating with Tylenol. Still having pain and redness at injection site. Muscles underneath right arm hurt all the time until 11/3. On 11/01 started getting fever blisters all over mouth, and they are still there. Now dealing with swollen lymp nodes on neck.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Generalized anxiety disorder, and obesity
- Andere Medikamente
- Lexapro, and Feynor (Birth Control)
- Allergien
- Reglan
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Chills
Decreased appetite
Fatigue
Injection site erythema
Injection site pain
Injection site rash
Musculoskeletal stiffness
Pain
Pain in extremity
Pyrexia
Sleep disorder
Somnolence
Symptomtext
Sore arm, pink circle w/ tiny white center at injection site. Soreness in arm got worse and evening progressed. Interfered with sleep. Did not take medication . Next day, 10/28/2021, no appetite, achy and stiff, tired, sleep off and on all day. Injections site reactions was bigger yet fainter, 1 1/2 to 2 inches around. Less painful, no trouble sleeping. 10/29/2021, sore arm and arm pit. Still tired, possible chills. Small pink circle with red center at injections site. On inside of arm, 2inch above and 3 to 4 inches below injection site, there was blotchy light pink rash. No itch with rash. Slightly feverish overnight. 10/30/2021, rash was darker pink and achy. Slight chills. Temperature 1 degree higher than normal. Overnight, slightly feverish, slept well. 10/31/2021, briefly feverish No longer had underarm tenderness. Sore arm was gone. Covid rash was barely visible. 11/01/2021 all symptoms resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Covid arm, Osteopenia
- Andere Medikamente
- Calcium 600mg w/ Vitamin D3 800 IU 2x daily, Vitamin B12 500mg 1x daily,
- Allergien
- Ibeprofin, Mold, Dust, Perfume, Dyes, Makeups, Poison Ivy
- Vorherige Impfungen
- 1st and 2nd Covid shots 02/2021, 03/2021-Moderna
- Staat
- NJ
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 19.09.2021
- Beginn
- 02.10.2021
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Blood test normal
Burning sensation
Chills
Contusion
Lymphadenopathy
Pain
Pruritus
Pyrexia
Rash
Urticaria
Symptomtext
Had full dose given... had pretty extreme reaction. Fever, body aches, chills etc...swollen lymph node in left underarm swollen for 1-2 weeks and then the full body rash started and hasn't stopped since! It feels like burning sporadically all over body. Comes often and travels all over my body. Sometimes looks like hives and now starting to bruise sometimes and unrelated to any incident too. Still some body/joint aches too. But the itchy body symptoms are unbearable for nearly a month!!!!!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Full blood work drawn and now showing anything really abnormal.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Tylenol PM
- Allergien
- seasonal allergies and that is all I'm aware of at this time
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Injection site bruising
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Rash
Symptomtext
Site: Bruising at Injection Site-Severe, Site: Itching at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Error: Wrong Route (SC, IM, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 31.10.2021
- Impfdatum
- 20.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Impaired driving ability
Pain
Pyrexia
Symptomtext
Low grade fever; generally aches and pains; unable to operate any machinery including automobile lasting 36 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetic type 2
- Andere Medikamente
- Metformin: Lotrel
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 30.10.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Fatigue
Pyrexia
Symptomtext
22 hours post vaccination- high fever, chills, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, migraines
- Andere Medikamente
- -
- Allergien
- Voltaren
- Vorherige Impfungen
- COVID - Moderna- 2nd Dose
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Injection site warmth
Pyrexia
Symptomtext
Injection site: red, painful, swelling, itching, warm to the touch. Itch started around the 7-10 minute mark after injection. Pretty intense for about 20 minutes, then subsided to almost nothing for several hours, then increased, but was bearable. Redness started almost immediately. Redness spread to about 3 inches in diameter from shot site. (Still present as of 10/29 evening). Still present on 10/29 evening: redness, itch, warm to the touch. Started taking Claritin (antihistamine) on Tuesday morning. Ran a low fever all day Tuesday, but fever increased and so did fatigue. Went to bed early (8 p.m.) and fever broke around 2 a.m. Wednesday morning. Fatigue continued through Wednesday and Thursday. Fatigue mostly gone by 10/29 morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Asthma. Obesity.
- Andere Medikamente
- Vitamin D3, Vitamin B12, Probiotic, Evening Primrose Oil capsule, and women's multivitamin. Estradiol .05mg patch.
- Allergien
- Intolerance to nightshade vegetables.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 23.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cellulitis
Extra dose administered
Injection site swelling
Injection site warmth
Vaccine positive rechallenge
Symptomtext
Site was swollen and very warm - celulitis - antibiotics for a week and getting better
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- acid reflux
- Andere Medikamente
- Premarin and Protonix
- Allergien
- none
- Vorherige Impfungen
- shingrex - 1st dose similar reaction - not as bad - antibiotics not . needed. around september of 2018 or 2019. 55 or 56 years
- Staat
- VA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Decreased appetite
Fatigue
Headache
Myalgia
Nausea
Pyrexia
Symptomtext
High fever, nausea, loss of appetite, no strength, terrible headache, muscle ache, and fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- High blood pressure
- Vorgeschichte
- High blood pressure, heart (4 stents), digestive problems
- Andere Medikamente
- Heart medication, blood pressure medication, hiatal hernia medication, antacid
- Allergien
- -
- Vorherige Impfungen
- The second dose
- Staat
- AR
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 26.09.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Coagulation test normal
Full blood count normal
Herpes zoster
Metabolic function test normal
Rash
Red blood cell sedimentation rate normal
Symptomtext
Shingles like rash on both legs, inside near knee that has lasted two weeks. Rx hydrocortisone calmed it down, but still visible.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- CBC,CMP, Sed Rate , ESR and coagulation tests all normal
- Aktuelle Erkrankungen
- This was the 3rd shot & booster, but no reaction like this on previous 2.
- Vorgeschichte
- Lupus, rheumatoid arthritis, Sjogren?s and Raynauds, migraines, central sleep apnea, peripheral neuropathy, fatigue, INS, GERD,
- Andere Medikamente
- Aimovig, b complex, Baclofen, DHEA, Zyrtec, Evoxac, cranberry, arocept, Cymbalta, famvir, , duragesic, fish oil, FML drops, Neurontin, Remicade, Arava, Singular, multi-vitamin, Nitrofurontin, Protonix, prednisone, probiotic, quitapine, Cres
- Allergien
- Erythromycin, bentyl, glue adhesive, minicin, benicar, Altace, sulfa, Zithromax, Wellbutrin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 23.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Calcinosis
Joint space narrowing
Knee deformity
Loose body in joint
Swelling
Vascular calcification
X-ray limb abnormal
Symptomtext
The night I received the vaccine my left knee started hurting me. To the best of my knowledge my knee was normal before. I got up and went to bathroom, upon standing up it really hurt. A few days later my right knee started hurting but in a different location. My doctor suggested that the vaccine might have stirred up an old injury causing swelling. That might have contributed to the results (see below)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- X-Ray 10-22-21 results 15 mm ovoid calcific versus ossified intra-articular loose body projects just anterior to the left tibial spines. Tripartile left patella. Left knee with medial compartment joint space narrowing. Dense vascular calcifications. MRI scheduled next week.
- Aktuelle Erkrankungen
- Before first vaccination I developed MMP (Mucous Membrane Pemphigoid)
- Vorgeschichte
- none
- Andere Medikamente
- No prescriptions 2000 mg numeric 2000 mg vit D 1000 mg calcium 1000 mg Niacinamide 500 mg Potassium 400 mg magnesium 3 mg melatonin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 26.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Impaired work ability
Loss of personal independence in daily activities
Myalgia
Pyrexia
Symptomtext
High fever (103), severe joint and muscle pain, full loss of ADLs and unable to work at all.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Cholesterol and blood pressure
- Andere Medikamente
- Zyrtec, atorvastatin, amlodipine and valsartan
- Allergien
- Almonds
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash pruritic
Symptomtext
Itchy rash in the form of a big bumps all over my body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- I haven?t taken any test yet I have a doctors appointment in the morning.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
Heart rate
Malaise
Rash
Vaccination site pain
Wheezing
Symptomtext
soreness of the Left Arm (vaccination site); wheezing; rash in the groin area; said he is not feeling well; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (said he is not feeling well), WHEEZING (wheezing), RASH (rash in the groin area) and VACCINATION SITE PAIN (soreness of the Left Arm (vaccination site)) in a 37-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. The patient's past medical history included Asthma (He had no attacks for 10 years now. But he has one Asthma Inhaler for emergency purposes.). On 19-Oct-2021 at 6:00 PM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In October 2021, the patient experienced MALAISE (said he is not feeling well). On 19-Oct-2021, the patient experienced WHEEZING (wheezing) and RASH (rash in the groin area). On 19-Oct-2021 at 9:00 PM, the patient experienced VACCINATION SITE PAIN (soreness of the Left Arm (vaccination site)). At the time of the report, MALAISE (said he is not feeling well) and WHEEZING (wheezing) had not resolved and RASH (rash in the groin area) and VACCINATION SITE PAIN (soreness of the Left Arm (vaccination site)) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In October 2021, Blood pressure measurement: 148/94 (abnormal) 148/94. In October 2021, Heart rate: 86 (normal) pulse rate of 86. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant medications were reported. Patient used his unspecified Asthma inhaler for the event wheezing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Test Date: 202110; Test Name: Blood pressure; Result Unstructured Data: 148/94; Test Date: 202110; Test Name: pulse rate; Result Unstructured Data: pulse rate of 86
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma (He had no attacks for 10 years now. But he has one Asthma Inhaler for emergency purposes.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 24.09.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 26,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Pruritus
Rash
Urticaria
Symptomtext
Rash and small hives appeared on upper chest, groin and both forearms on October 20, In next few days rash expanded to 50% of body including hands, arms, legs and back with intense itch in the extremities (hands and feet) Treatment with Prednisone and Benadryl over the next four days successfully treated most symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Immunology issues eczema, interstitial cystitis, bee venom allergy
- Andere Medikamente
- Simvastatin, ezetimibe, dutasteride AREDS2 D3, B-12, multi-vitamins
- Allergien
- MRI contrast dye
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 26.10.2021
- Impfdatum
- 23.10.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Asthenia
Chills
Fatigue
Flushing
Pyrexia
Symptomtext
Woke up with chills and fever at 3am after injection (which was given at 10:30am the day before), with sore joints and facial flushing. Took two Tylenol and went back to sleep. Felt tired and somewhat weak the next day, but recovered quickly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prilosec, Mobic
- Allergien
- Sulfa
- Vorherige Impfungen
- Previous Moderna vaccine reactions were much milder
- Staat
- TN
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 25.10.2021
- Impfdatum
- 23.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Continuous sore arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Juice plus gummies
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 25.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dysgeusia
Nausea
Parosmia
Symptomtext
Metallic taste in mouth. Sense of smell changed. Nausea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Seasonal allergies
- Vorgeschichte
- Arthritis Obesity
- Andere Medikamente
- Methocarbamol 750 mg Levothyroxine 75 mg Rosuvastatin 10mg Linsinopril 5 mg Calcium 600 mg Multi Vitamin Magnesium 400 mg Vitamin C 100 mg
- Allergien
- Levaquin Mold Dust Pine Iodine wash Casein
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 24.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pain in extremity
Peripheral swelling
Skin warm
Symptomtext
Localized pain, heat swelling rt. arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Atorvastatin. Lasix.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 24.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Extra dose administered
Injection site swelling
Lymphadenopathy
Symptomtext
Swelling and pain in my armpit on the same side as the vaccine dose was given. Swelling at injection site worse over time (this is just for your information as the concern is the armpit swelling/pain). The armpit swelling/pain was not experienced during the first or second vaccine dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- Overweight
- Andere Medikamente
- Ibuprofen and NyQuil last dose 8 hours before I noticed swelling and pain under my arm.
- Allergien
- Mild to lactose and cider pollen
- Vorherige Impfungen
- Typhoid Fever (red spots or hives over upper body) late 2018) taken with first Hep B/A vaccine
- Staat
- MA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 23.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hyperhidrosis
Incorrect dose administered
Pyrexia
Symptomtext
Sweats fever Was given 0.5 ml dose instead of 0.25 ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None No illness, just an injury broken finger
- Vorgeschichte
- Type 2 diabetes
- Andere Medikamente
- Metformin 500 mg qd
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 22.10.2021
- Impfdatum
- 20.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood test
Diarrhoea
Dizziness
Feeling abnormal
Gait disturbance
Headache
Influenza like illness
Nausea
Nervousness
Pyrexia
SARS-CoV-2 test
Vomiting
Symptomtext
Began with flu like aches and pains around 3 AM the morning after receiving injection. Around 11 AM on 10/22/21 I couldn't stop vomiting. I was unable to take sips of water without it immediately coming back up. Around 3 PM I was very shaky, weak, dizzy, and had intense brain fog and had a fever on and off throughout the day. Around 7 PM I went to the emergency room for treatment and could hardly walk due to weakness. 10/22/21 I woke up with nausea and a headache and have had diarrhea throughout the day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- I was given 2 L of IV fluid, Zofran, and tylenol. They took a blood panel to check my electrolytes, and I received a COVID test. Was sent home with a prescription for Zofran should nausea persist.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- zyrtec, prenatal vitamin, prozac
- Allergien
- latex, fentanyl, severe seasonal allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 21.10.2021
- Impfdatum
- 17.10.2021
- Beginn
- 17.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Symptomtext
Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Medium, Additional Details: Pt reports redness and itchiness at injection site. Told pt to put some ice on it and take otc pain medication and speak with prescriber if there isn't any resolution.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 21.10.2021
- Impfdatum
- 20.10.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Asthenia
Confusional state
Immediate post-injection reaction
Injection site erythema
Injection site pain
Pain
Symptomtext
Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Systemic: Abdominal Pain-Severe, Systemic: Body Aches Generalized-Severe, Systemic: Confusion-Medium, Systemic: Weakness-Medium, Additional Details: All symptoms were immediate after vaccination within 30-100 seconds. Ambulance was called and pt slightly recovered when EMS arrived. Pt. was worked up by paramedics and walked out with them not on stretcher- unsure of outcome after leaving pharmacy. Additional symptom not listed: RIGHT arm pain, when injection was given in left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 20.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Injection site cellulitis
Injection site erythema
Injection site pruritus
Symptomtext
Cellulitis at injection site. Redness, itching
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Omeprazole
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 20.10.2021
- Impfdatum
- 16.10.2021
- Beginn
- 16.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site urticaria
Pruritus
Urticaria
Symptomtext
Hives at injection site and on face; itchiness at injection site and on face. Cool clothes on face and Benadryl. Hives subsided from face 1.5 hours later; not injection site. Hives subsided from injection site on Monday 10/18. Injection site still itchy, red and less sore.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma, Allergies, Eczema, Pericarditis
- Andere Medikamente
- Vitamin D, Xyzal, Echinacea
- Allergien
- Lactose Intolerance
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 17.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Drainage
Erythema
Peripheral swelling
Pruritus
Symptomtext
arm - red swollen and had a draining affect - patient also stated that it was itchy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 13.10.2021
- 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 mass
Injection site warmth
Symptomtext
LUMP IN AREA OF INJECTION ON LEFT ARM, WARM TO TOUCH RED APPEARANCE , RESOLVED IN 48 HOURS AFTER TAKING DIPHENHYDRAMINE AND ACETAMINOPHEN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetes
- Andere Medikamente
- diphenhydramine, acetaminophen
- Allergien
- none listed
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 15.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Vomiting
Symptomtext
Systemic: Nausea-Medium, Systemic: Vomiting-Medium, Additional Details: pt threw up and was very nausious after 5 min of injectoins
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chills
Cough
Fatigue
Feeling abnormal
Headache
Nausea
Pyrexia
Vaccination site pain
Symptomtext
woke up feeling really crappy; dry cough for several hours that subsided periodically; felt nauseous; had chills last night; she felt okay, but had some fatigue; low fever max 98.6; massive headache; pain at injection site; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (woke up feeling really crappy), COUGH (dry cough for several hours that subsided periodically), NAUSEA (felt nauseous), CHILLS (had chills last night) and FATIGUE (she felt okay, but had some fatigue) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included BUPROPION and BUSPIRONE for an unknown indication. On 05-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Oct-2021, the patient experienced VACCINATION SITE PAIN (pain at injection site). On 06-Oct-2021, the patient experienced FEELING ABNORMAL (woke up feeling really crappy), COUGH (dry cough for several hours that subsided periodically), NAUSEA (felt nauseous), CHILLS (had chills last night), FATIGUE (she felt okay, but had some fatigue), PYREXIA (low fever max 98.6) and HEADACHE (massive headache). The patient was treated with ASPIRIN [ACETYLSALICYLIC ACID] for Headache, at an unspecified dose and frequency. At the time of the report, FEELING ABNORMAL (woke up feeling really crappy), NAUSEA (felt nauseous), CHILLS (had chills last night), FATIGUE (she felt okay, but had some fatigue) and PYREXIA (low fever max 98.6) outcome was unknown and COUGH (dry cough for several hours that subsided periodically), VACCINATION SITE PAIN (pain at injection site) and HEADACHE (massive headache) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: 98.6 (High) 98.6.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: 98.6
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- BUPROPION; BUSPIRONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- 06.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Fatigue
Feeling hot
Hunger
Hyperhidrosis
Impaired work ability
Pyrexia
Somnolence
Symptomtext
Dizzy; Can hardly do anything; Sweat; Very hot; Really sleep; Hungry; Fever; Fatigue; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (Dizzy), IMPAIRED WORK ABILITY (Can hardly do anything), HYPERHIDROSIS (Sweat), FEELING HOT (Very hot) and SOMNOLENCE (Really sleep) in a 35-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 in July 2020. On 06-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Oct-2021, the patient experienced DIZZINESS (Dizzy), IMPAIRED WORK ABILITY (Can hardly do anything), HYPERHIDROSIS (Sweat), FEELING HOT (Very hot), SOMNOLENCE (Really sleep), HUNGER (Hungry), PYREXIA (Fever) and FATIGUE (Fatigue). The patient was treated with PARACETAMOL (TYLENOL 8 HOUR) at an unspecified dose and frequency. At the time of the report, DIZZINESS (Dizzy), IMPAIRED WORK ABILITY (Can hardly do anything), HYPERHIDROSIS (Sweat), FEELING HOT (Very hot), SOMNOLENCE (Really sleep), HUNGER (Hungry), PYREXIA (Fever) and FATIGUE (Fatigue) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. About 20 minutes after the vaccination patient stated experiencing fever, dizzy, sweat, very hot, really sleepy, hungry, fatigue, and she can hardly do anything. She took Tylenol extra strength . She had COVID-19 in JULY 2020 and she has had more symptoms with the vaccine than when she had COVID-19. No concomitant medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 14.10.2021
- Impfdatum
- 11.10.2021
- Beginn
- 13.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Induration
Pruritus
Swelling
Tenderness
Symptomtext
Have a bullseye on her left arm about 3 to 4 inches long. Its red and raised and underneath it, it feels hard and itchy. Kind of tender and swollen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- brain injury, kidney problems and ashtma
- Andere Medikamente
- Bupropion hcl xl 150mg , Amlodipine 5mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 14.10.2021
- Impfdatum
- 11.10.2021
- Beginn
- 12.10.2021
- 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 pain
Injection site swelling
Injection site warmth
Lymph node pain
Symptomtext
I receive the 2nd dose around 1230the afternoon of oct 11th and that afternoon it made it to a small quarter sized red spot at injection site and very sore arm. By the end of the 2nd day the red spot was about half dollar size and lymph nodes in under arm tender. The next day I woke up and the spot was about 2inches wide and about 3.5inches long and my nodes in my underarm were tender.the injection site was swollen And warm .And today 10/14/2021 the red spot is about 4inches wide and about 5inches long still very swollen warm and underarms are extremely sore. I called physician was told to show pharmacist where vacc. Was administered. Was told by pharm to take Benadryl
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- GERD. Gastroparesis. Hiatal hernia esaphageal erosion
- Andere Medikamente
- Eledel cream
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 30.09.2021
- Beginn
- 08.10.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Rash erythematous
Symptomtext
Patient reported experiencing rash around and at the injection site. Reports "nasty red rash"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Promethazine Atenolol Levothyroxine Junel
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 26,0
- 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
Arthralgia
Body temperature increased
Feeling of body temperature change
Headache
Muscular weakness
Nausea
Pain
Symptomtext
Temperature of 99.9?F. Severe headache. Nausea. Lower half of body feels like its freezing and the top half feels like it is burning up. Every joint and body aches. Upper left arm muscles is weak.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Tylenol
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 12.10.2021
- Impfdatum
- 04.10.2021
- Beginn
- 11.10.2021
- 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 nodule
Injection site pain
Injection site swelling
Symptomtext
Received moderna vaccine 8 days ago, yesterday the injection site became red and swollen and somewhat painful. Knot the size of an orange.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Wellbutrin, Viibryd, Concerta
- Allergien
- Bactrum, Amoxicillin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 10.10.2021
- Impfdatum
- 09.10.2021
- Beginn
- 09.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Injection site pruritus
Pruritus
Symptomtext
Site: Itching at Injection Site-Medium, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Itch Generalized-Medium, Systemic: Dizziness / Lightheadness-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 07.10.2021
- Impfdatum
- 27.09.2021
- Beginn
- 04.10.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site induration
Injection site nodule
Injection site pruritus
Injection site warmth
Symptomtext
one week after the shot patient had warmth , itching and a hard knot at the injection site , Dr . called it Covid arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site induration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- alprazolam 0.5 mg
- Allergien
- latex , eggs
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 04.10.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cyanosis
Headache
Peripheral swelling
Pyrexia
Rash
Symptomtext
Pt had rash over entire body and swelling/ turning blue of her legs and hands. Also headache and slight fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- pt had covid in July 2021 nothing 30 days prior to vaccination
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- ibuprofen
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 26.09.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Peripheral swelling
Pruritus
Skin warm
Swelling
Symptomtext
Started with a raised bump 8 days after injection. The following day my arm is red, very swollen, itchy, and warm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Decreased appetite
Fatigue
Nausea
Pyrexia
Symptomtext
Pt. states that after receiving the 3rd dose of Booster Moderna 09/30/2021, started experiencing symptoms 09/30/2021 of chills, fever, nausea, fatigue, loss of appetite, and dry cough. Still continuing to experience symptoms, Primary communications still waiting for recommendations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Immunocompromised, HBP, High Cholesterol, PMR Arthritis
- Andere Medikamente
- Extra-Strength Tylenol, Prednisone 5mg, Lisaprenaprol, Hydrochlorothiazide, Amistad, Aumapramazal, Astrozal
- Allergien
- Cipro, Arithamicine
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 24.09.2021
- Beginn
- 02.10.2021
- Tage bis Beginn
- 8,0
- 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
Symptomtext
Red itchy and swollen area over the injection site. It started 8 days after the vaccination and has been occuring for 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling hot
Hyperhidrosis
Rash
Rash erythematous
Symptomtext
Bright red rash appeared on over 50% of back on the evening of the day of vaccination, and gradually darkened over the following days. Patient also reported feeling hot/sweating over time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seasonal Allergies
- Andere Medikamente
- Zyrtec 10mg
- Allergien
- Patient says she has an allergy to a filler that is used in some medications, but could not recall the name
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 22.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Influenza like illness
Pain
Rash macular
Skin exfoliation
Urticaria
Symptomtext
First red blotch approx. 7 hours after shot. Some pain, no itching. Then larger "welt" (about 2'x3') developed lasting several days. Finally diminishing to light red spot about the size of half dollar. Then skin pealed in area of welt.. Slight redness still persists after 12 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- RA
- Andere Medikamente
- Azulfidine Entabs), Benicar Tabs, Low Dose Aspirin 81 mg , Calcium 1200 mg/D-3, Omega-3 1200 mg , Vitamin D3 25 mcg / 1000 IU Potassium 550 mg , B-12 1000 mcg , Vitamin C 250 , Prilosec, Probiotic Ortho Dophilus
- Allergien
- : Leflunomide (disease-modifying antirheumatic drug (DMARD) that is used to treat rheumatoid arthritis) Brand Name: Arava
- Vorherige Impfungen
- Developed Covid Arm after first Moderna shot. And flu like symptoms for two days after second shot. PS. Also had flu like sympto
- Staat
- CT
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 02.10.2021
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Systemic: Allergic: Rash Generalized-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 02.10.2021
- Impfdatum
- 21.09.2021
- Beginn
- 21.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Injection site erythema
Injection site pruritus
Malaise
Pain
Vaccination site mass
Vaccination site swelling
Symptomtext
Feel weak; Feel sick; it started to swell up below the injection site in a lemon sized lump; little red circles; Sarted itching like crazy; This area continued to stay swollen and itchy; Pain in patient's arm which worsened; This spontaneous case was reported by a patient and describes the occurrence of PAIN (Pain in patient's arm which worsened), ASTHENIA (Feel weak), MALAISE (Feel sick), VACCINATION SITE MASS (it started to swell up below the injection site in a lemon sized lump) and INJECTION SITE ERYTHEMA (little red circles) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 21-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Sep-2021, the patient experienced PAIN (Pain in patient's arm which worsened). On 22-Sep-2021, the patient experienced ASTHENIA (Feel weak), MALAISE (Feel sick), VACCINATION SITE MASS (it started to swell up below the injection site in a lemon sized lump), INJECTION SITE ERYTHEMA (little red circles), INJECTION SITE PRURITUS (Sarted itching like crazy) and VACCINATION SITE SWELLING (This area continued to stay swollen and itchy). The patient was treated with NAPROXEN SODIUM (ALEVE) for Adverse event, at an unspecified dose and frequency. At the time of the report, PAIN (Pain in patient's arm which worsened), ASTHENIA (Feel weak), MALAISE (Feel sick), VACCINATION SITE MASS (it started to swell up below the injection site in a lemon sized lump), INJECTION SITE ERYTHEMA (little red circles), INJECTION SITE PRURITUS (Sarted itching like crazy) and VACCINATION SITE SWELLING (This area continued to stay swollen and itchy) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medications were not provided by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 30.09.2021
- Impfdatum
- 28.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Headache
Pain
Symptomtext
Chills, fatigue, aches all over, headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 29.09.2021
- Impfdatum
- 25.09.2021
- Beginn
- 25.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Decreased appetite
Fatigue
Headache
Nausea
Pain
Symptomtext
Severe fatigue, body aches, chills, nausea, headache, decreased appetite.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Bronchitis & Depression
- Andere Medikamente
- None
- Allergien
- Minocycline and Sulfa antibiotics
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 29.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- 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
Fatigue
Interchange of vaccine products
Lethargy
Pain
Symptomtext
Systemic: Body Aches Generalized-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Weakness-Medium, Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 25.09.2021
- Beginn
- 25.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
Pt called stating she has having increased swelling and redness at injection site since administration of her second Moderna vaccine on 9/25/21. Pt stated she has tried oral/topical Benadryl, Tylenol, and iced down the area. She stated she had a bit of swelling after the first vaccine, but it is worse this time. She also stated that she has an adhesive allergy and she took off the bandage sooner after the first vaccine than she did after the second vaccine. I advised that injection site swelling/redness are common side effects but recommended she follow-up with her pcp regarding this. I also recommended she try ibuprofen as well for pain/inflammation. I requested pt follow-up with us to let us know how she is doing, she stated she would.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 26.09.2021
- Beginn
- 26.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injection site swelling
Peripheral swelling
Symptomtext
Site: Swelling at Injection Site-Severe, Additional Details: arm very swollen - entire length arm. no other side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 25.09.2021
- Impfdatum
- 18.09.2021
- Beginn
- 18.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 24.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- 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
Nausea
Symptomtext
I gave the vaccine, after the vaccine was completed. I told the patient to sit in the waiting area for 15 minutes, so we can monitor. However, less than 5 minutes, the patient was feeling dizziness. He was still conscious though. His girlfriend was next to him. He stated he was nausea, dizziness, sweating, and he wanted to pass out. We went and got him water and make sure he was okay. Afterward, we monitor him for additional 30 minutes. He felt better after he drank his water, ate a few candies, and a donut. He stated the last he ate was at 10am and only had a granola bar. We let him leave after he felt better. Before, we left him leave. We asked him if he is allergic to any type of medications and if he had ever fainted after a vaccine. He stated, he is not allergic to medication and he never fainted after a vaccine before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- He said he has no medical condition.
- Vorgeschichte
- No medical condition.
- Andere Medikamente
- Patient stated he only ate a granola bar at 1000am.
- Allergien
- He stated he is not allergic to medications or food.
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 24.09.2021
- Impfdatum
- 23.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site bruising
Injection site swelling
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Followed up with patient 4-6hrs after and he said no changes reported and he feels fine, I iced the injection site for about 2-3mins and kept checking on him. He didn't report any pain or discomfort, just bruising and swelling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 19.09.2021
- Impfdatum
- 17.09.2021
- Beginn
- 17.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Erythema
Headache
Peripheral swelling
Pruritus
Rash
Tenderness
Symptomtext
3 hours after shot the patient got a headache and the patient's arm started to swell and become tender and red. 2 days post shot her arm started to swell even more despite icing it. she developed a red streak down her arm they continued to widen and lengthen and she developed little bug bite like bumps on her vaccinated arm the burned and itched. She was advised to take ibuprofen, continue to ice and take Zyrtec since she can't tolerate Benadryl and she will go to her PCP tomorrow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- earache a week before, was well at time of shot
- Vorgeschichte
- COPD chronic bronchitis
- Andere Medikamente
- montelukast 10mg
- Allergien
- peanuts flexeril kiwi
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 19.09.2021
- Impfdatum
- 18.09.2021
- Beginn
- 18.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chills
Heart rate increased
Myalgia
Pruritus
Skin warm
Urticaria
Vaccination complication
Symptomtext
Hives started within 2 hours (Benadryl), arm hot to touch, elevated heart rate (98 at resting, typically at 58-65), itchiness throughout the body, muscle soreness, severe chills (negative for fever), chest tightness (O2 stat; 97), COVID Arm?.took ibuprofen and it just helped minimize the symptoms but didn?t not take the issues away, welt on arm has grown from last night and is very hot to touch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- No tests at this time, if they symptoms do not get better around the 12 hour range, I will be going to urgent care.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Post thrombosis syndrome, May turners syndrome
- Andere Medikamente
- Xarelto- for DVT?s
- Allergien
- Latex, silicone, parabins, avocado, tomato, banana, mangos, Kiwi,
- Vorherige Impfungen
- Moderna (8/21/21 ) body aches, headache.
- Staat
- WI
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 18.09.2021
- Impfdatum
- 18.09.2021
- Beginn
- 18.09.2021
- 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
Nausea
Pallor
Symptomtext
He became very dizzy and nauseous. Felt like he had to vomit but did not. Was sweaty and pale. He then told me he had had a similer reaction to a flu shot . (did not indicate this on consent form) Offered to help him lie down but at first refused and held garbage can. got him a cold pack and convinced him to lie down. he did for just a few minutes, then sat up and said he felt much better. I talked to him and he was always coherent and aware of what was going on. The 15 minute timer went off while he was sitting on the floor and wanted to get back into chair. and color returned to normal. A friend was with him in store, he called her to come to the pharmacy area. Ther sat for a while, I talked to them and since he seemed steady on his feet, the left together .Total time was 25-30 minutes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- diabetes
- Andere Medikamente
- Venlafaxine ER 150mg, Gabapentin 600mg, Metformin 1000mg, glipizide 10 mg, atorvastatin 40mg
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 22.05.2023
- Impfdatum
- 27.09.2021
- Beginn
- 19.05.2022
- Tage bis Beginn
- 234,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Neuropathy peripheral
Symptomtext
PERIPHERAL NEUROPATHY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neuropathy peripheral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 11.05.2023
- Impfdatum
- 05.11.2021
- Beginn
- 23.02.2022
- Tage bis Beginn
- 110,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Coagulopathy
Diabetic nephropathy
Symptomtext
D68.9 COAGULOPATHY, UNSPECIFIED TYPE 2/23/2022 DM 2 W RENAL MANIFESTATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Coagulopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 09.05.2023
- Impfdatum
- 12.04.2021
- Beginn
- 26.04.2021
- Tage bis Beginn
- 14,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Colitis
Symptomtext
Pt had covid RNA gene therapy in April 2021 and 12/21; first J&J then Moderna.. After first vaccine had a colitis flare treated with steroids and mesalamine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Colitis
- Hospital-Tage
- -
- Labordaten
- see attached
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Other adrenocortical insufficiency, esophagitis, unspecified, other dietary vitamin B12 deficiency anemia, hormone
- Andere Medikamente
- progesterone; valacyclovir; Methyl B Complex; Intramax; Topamax; Pure Encapsulation magnesium glycinate; Medi Herb Fe-Max Iron; Cymbalta; ondansetron; Climara; MESALAMINE DR; Methylcobalamin; naltrexone; testosterone powder; Synthroid; traz
- Allergien
- Codeine, morphine,sulfa
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 27.01.2023
- Impfdatum
- 05.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Adverse event: moderate bilateral tinnitus Treatment: masking, mindfulness-based stress reduction Outcome: habituation, decreased prominence but still perceivable currently
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Seasonal allergies Hearing loss actively treated with hearing aids
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Hives, age 19, 4/25/2000, hepatitis B vaccine #2 in series
- Staat
- CT
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 20.08.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 134,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
Contracted COVID in 1/1/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive Antigen Test
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- multiple sclerosis
- Andere Medikamente
- Zyrtec; Vumerity
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 19.12.2022
- Impfdatum
- 09.09.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 119,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Systemic lupus erythematosus
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Systemic lupus erythematosus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 08.10.2022
- Impfdatum
- 25.10.2021
- Beginn
- 29.09.2022
- Tage bis Beginn
- 339,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after three vaccines Moderna 1/20/21 Lot# 029L20A; Moderna 2/17/21 Lot# 024M20A; Moderna 10/25/21 Lot# 061E21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- U
- Eingang
- 11.08.2022
- Impfdatum
- 01.10.2021
- Beginn
- 21.07.2022
- Tage bis Beginn
- 293,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
HSOPITALIZED WITH COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 12,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 49,0
- Dosis
- 4
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Osteoporosis, periodic atrial fibrillation
- Andere Medikamente
- Eliquis 5mg bid; metaprolol 12.5mg bid; Rosuvastan 2.5mg daily; Prolia tice yearly
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 08.10.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
X-ray
Symptomtext
COVID-19; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (COVID-19) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Penicillin. Past adverse reactions to the above products included Allergy with Penicillin. On 08-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced COVID-19 (COVID-19). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 25-May-2022 to 28-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (COVID-19) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, X-ray: result not provided Result not provided. Concomitant medication was not reported. Patient was not taking other medications/products within 2 weeks of starting COVID-19 treatment. Patient previously received a COVID-19 Vaccine. Device Date was reported as '29May2022'. Company Comment: This spontaneous case concerns a 65-year-old, female patient with no relevant medical history reported, who experienced the unexpected, non-serious AESI of COVID-19. The event occurred approximately 7 months after receiving the third dose of the mRNA-1273 vaccine. The patient took Paxlovid (nirmatrelvir, ritonavir) for 4 days only (25May2022 to 28May2022). It was reported that 1 day after taking Paxlovid, the patient woke up with a terrible feeling of throat swelling and intense throat pain (pain scale: 10/10). She had trouble breathing and wheezing, and could not lay down or the symptoms got worse. She gargled with salt water and took Tylenol (paracetamol) affording no relief of symptoms. She lost her voice and the swelling got worse. The following day, the patient went to the Emergency department. X-rays (unspecified) were done, however, the results were not provided. The patient was given an unspecified medicine to reduce the swelling. It was reported that the doctors did not consider an allergic reaction to Paxlovid. The doctors were concerned to stop the antiviral therapy but eventually the patient was told to stop taking the drug. The patient took Benadryl (diphenhydramine) which afforded relief from the throat swelling. Five days after the first dose of Paxlovid, the patient cannot speak beyond a whisper and the throat pain still continued. Additionally, the patient was also treated with Toradol (ketorolac), Duoneb (ipratropium bromide/salbutamol) and Decadron (dexamethasone). The patient's advanced age (high risk for infections) remains a confounder for the event COVID-19. The benefit-risk relationship of the mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This spontaneous case concerns a 65-year-old, female patient with no relevant medical history reported, who experienced the unexpected, non-serious AESI of COVID-19. The event occurred approximately 7 months after receiving the third dose of the mRNA-1273 vaccine. The patient took Paxlovid (nirmatrelvir, ritonavir) for 4 days only (25May2022 to 28May2022). It was reported that 1 day after taking Paxlovid, the patient woke up with a terrible feeling of throat swelling and intense throat pain (pain scale: 10/10). She had trouble breathing and wheezing, and could not lay down or the symptoms got worse. She gargled with salt water and took Tylenol (paracetamol) affording no relief of symptoms. She lost her voice and the swelling got worse. The following day, the patient went to the Emergency department. X-rays (unspecified) were done, however, the results were not provided. The patient was given an unspecified medicine to reduce the swelling. It was reported that the doctors did not consider an allergic reaction to Paxlovid. The doctors were concerned to stop the antiviral therapy but eventually the patient was told to stop taking the drug. The patient took Benadryl (diphenhydramine) which afforded relief from the throat swelling. Five days after the first dose of Paxlovid, the patient cannot speak beyond a whisper and the throat pain still continued. Additionally, the patient was also treated with Toradol (ketorolac), Duoneb (ipratropium bromide/salbutamol) and Decadron (dexamethasone). The patient's advanced age (high risk for infections) remains a confounder for the event COVID-19. The benefit-risk relationship of the mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: X-ray; Result Unstructured Data: Result not provided
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 28.09.2021
- Beginn
- 16.02.2022
- Tage bis Beginn
- 141,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood alkaline phosphatase increased
Blood test abnormal
Blood thyroid stimulating hormone
Differential white blood cell count
Fasting
Free thyroxine index
Full blood count
Inappropriate schedule of product administration
Lumbar puncture
Metabolic function test
Protein total
Tri-iodothyronine uptake decreased
Symptomtext
02/16/2022, I had my blood work done and I had 3 things that are out of range that my entire life has never been out of range before. Alkaline phosphate- 128 - it was high, T-3 uptake - 18 - was low, Free thyroxine index- 1.1 - which is low. The doctor would like to have it my blood work retaken in 3 months. I had never had any of these abnormalities before, my diet has not changed, my medications have not changed in the last 10 years. No treatment at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood alkaline phosphatase increased
- Hospital-Tage
- -
- Labordaten
- blood work - result on CMP, LP, TP, TSH, CBC - D, CLT and it was fasting
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Allergies, bulging disc in my neck, I take medication for it.
- Andere Medikamente
- Prozac, Amlodipine, Lisinopril, Zyrtec, Montelukast/Singulair, Vitamin E
- Allergien
- No, just environmental allergies
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 26.03.2022
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient came in on 10/26/2021 to received 3rd dose immunocompromised Covid Vaccine. Patient should have received Moderna 0.5mL, however received 0.25mL booster dose. Informed patient of this error upon arrival today for their "booster" dose, spoke with medical director. Medical director gave permission to give their 0.5mL dose today and report to VAERS. Patient refused to get 0.5mL as he states he is not particularly an advocate for vaccines and would prefer to just receive another half dose (0.25mL). I informed him that this is not recommended by the CDC for immunocompromised patients but he states a little bit is better than none or be given to much.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- self attests to immunocompromised condition.
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 26.03.2022
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Patient came in on 10/26/2021 to received 3rd dose immunocompromised Covid Vaccine. Patient should have received Moderna 0.5mL, however received 0.25mL booster dose. Informed patient of this error upon arrival today for their "booster" dose, spoke with medical director. Medical director gave permission to give their 0.5mL dose today and report to VAERS. Patient's father refused to get 0.5mL as he states he is not particularly an advocate for vaccines and would prefer to just receive another half dose (0.25mL). I informed him that this is not recommended by the CDC for immunocompromised patients but he states a little bit is better than none or be given to much.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Down Syndrome, patient self attests to immunocompromised per Dad
- Andere Medikamente
- n/a
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 25.10.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 25,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Delivery
Exposure during pregnancy
Normal labour
Symptomtext
Normal labor and delivery on 11/19/2021. Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Delivery
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 20.03.2022
- Impfdatum
- 25.09.2021
- Beginn
- 25.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint injury
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Joint injury
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 09.03.2022
- Impfdatum
- 10.11.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided 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. The vaccine was moved to refrigerator on 06/Oct/21. Total duration of temperature excursion is 4 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. On 06 Oct 2021, Both 5.5 ml and 7.5 ml vials were received in partially thawed/liquid condition vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 8 degree Celsius, total duration of the excursion refrigerated temperature for maximum of 4 hours. No concomitant medications was provided by the reporter. No treatment medications was provided by the reporter. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. No treatment medication were reported. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The vial was moved to fridge on 06-Oct-2021. PAT_MRN_ID was reported as 06011954 It was unknown that if the lot number undergone to temperature excursion on not. The state of the vaccine was partially thawed/liquid at the time of excursion. The vials size were 5.5 mL or 7.5 mL. Total duration of excursion was reported as maximus as 4 hours. No treatment medications were reported. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) and EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) and EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient MRN Id was 00557435. No concomitant medications were reported. No treatment medications were reported. It was reported that the vial was moved to fridge on 06-Oct-2021. The storage condition of the vial at the time of the excursion was frozen storage/refrigerated storage/ambient room temperature frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was reported as partially thawed/liquid. The maximum or minimum temperature reached by the vial was 8 degree Celsius. It was reported that the total duration of excursion at refrigerated temperature was for a maximum of 4 hours. It was reported that the vials were re-frozen. Temperature fluctuations had occurred from frozen state to refrigerated state to being re-frozen. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. On 06-Oct-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C. No treatment medications were reported. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) 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 medications were not reported. Treatment medications were not reported. The vial was moved to the fridge on 06 Oct 2021 and administered post 30 days from the initial storage at 2 degree Celsius to 8 degree Celsius. The facility thought that the vials were received frozen from Moderna, so they have been unpacking them and putting them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) and EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) and EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient MRN Id. No concomitant medications were reported. No treatment medications were reported. It was reported that the vial was moved to fridge on 06-Oct-2021. The storage condition of the vial at the time of the excursion was frozen storage/refrigerated storage/ambient room temperature frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was reported as partially thawed/liquid. The maximum or minimum temperature reached by the vial was 8 degree Celsius. It was reported that the total duration of excursion at refrigerated temperature was for a maximum of 4 hours. It was reported that the vials were re-frozen. Temperature fluctuations had occurred from frozen state to refrigerated state to being re-frozen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival/ total duration of the excursion refrigerated temps for max of 4 hrs; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge); This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival/ total duration of the excursion refrigerated temps for max of 4 hrs) and EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival/ total duration of the excursion refrigerated temps for max of 4 hrs). At the time of the report, PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival/ total duration of the excursion refrigerated temps for max of 4 hrs) and EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment information was reported. The vial was moved to the fridge on 06 October 2021 and administered post 30 days. The facility thought that the vials were received frozen from Moderna, so they have been unpacking them and putting them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient MRN id was reported. No concomitant medication was provided. It was unknown if the vial was undergone a previous temperature excursion. The storage condition at the time of the excursion was frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was partially thawed/liquid. The maximum temperature reached was 8?C. the total duration of the excursion refrigerated temps for max of 4 hours. The temperature fluctuations occurred as frozen-refrigerated and refrozen. On 06-OCT-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2 degree Celsius to 8 degree Celsius. Treatment medication was not provided by the reporter. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vial was moved to fridge on 06-Oct-2021. It was unknown that if the lot number undergone to temperature excursion on not. The state of the vaccine was partially thawed/liquid at the time of excursion. The vails size were 5.5 mL or 7.5 mL. Total duration of excursion was reported as maximus as 4 hours. 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
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival; Total duration of the excursion refrigerated temps for max of 4 hrs; They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge); This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product use was reported. Reporter stated that it was unknown if the vial was undergone a previous temperature excursion. The storage condition at the time of the excursion was frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was partially thawed/liquid. The maximum temperature reached was 8 degree Celsius. The total duration of the excursion refrigerated temperatures for max of 4 hours. The temperature fluctuations occurred as frozen-refrigerated and refrozen. And also stated that the vial was moved to the fridge on 06-Oct-2021 and administered post 30 days. No treatment information was provided. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- 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
Product temperature excursion issue
Symptomtext
Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival; Total duration of the excursion refrigerated temps for max of 4 hrs; They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge); This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) 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 (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. It was reported that, the vaccine was moved to fridge date was 06-OCT-2021. Vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 8-degree Celsius, total duration of the excursion refrigerated temperature for maximum of 4 hours. No treatment details were provided. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival; Total duration of the excursion refrigerated temps for max of 4 hrs; They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge); This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival), PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) and EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs). At the time of the report, PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival), PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) and EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. It was unknown, it this lot number undergone a previous temperature excursion; storage condition at the time of the excursion was frozen storage/refrigerated storage/ambient room temperature frozen storage/refrigerated storage; state of the vaccine at the time of the excursion was partially thawed/liquid, interim disposition of vials (returned to the freezer/refrigerator, or maintained at room temperature): frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival; inspection noting any vaccine state change (e.g. were frozen vials thawed, were thawed vials re-frozen, were they visualized at all): re-frozen and pertinent detail related to the impacted vial(s) (punctured/unpunctured or temperature fluctuations, etc.): temperature fluctuations, Frozen - refrigerated - re-frozen. Move to fridge date for the vaccine was 06-Oct-2021. No treatment information was provided by the reporter. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival; Total duration of the excursion refrigerated temps for max of 4 hrs; They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge); This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product information was not provided. Total duration of the excursion refrigerated temperature for maximum of 4 hour. On 06 Oct 2021, vial was moved to fridge. The facility thought that the vials are received frozen from Moderna so they had unpacked them and put them back into the facility freezer.They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. Vaccine administered post 30 days from the initial storage at 2 degree Celsius to 8 degree Celsius. Treatment information was not provided. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- 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
Product temperature excursion issue
Symptomtext
This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient MRN Id was 00422227. No concomitant medications were reported. No treatment medications were reported. It was reported that the vial was moved to fridge on 06-Oct-2021. The storage condition of the vial at the time of the excursion was frozen storage/refrigerated storage/ambient room temperature frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was reported as partially thawed/liquid. The maximum or minimum temperature reached by the vial was 8 degree Celsius. It was reported that the total duration of excursion at refrigerated temperature was for a maximum of 4 hours. It was reported that the vials were re-frozen. Temperature fluctuations had occurred from frozen state to refrigerated state to being re-frozen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) outcome was unknown. Not Provided. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No treatment medication was reported. No concomitant medication was reported. Vial was moved to fridge on 06-Oct-2021. Vaccine was administered past the 30-day from the initial storage at 2 degree Celsius to 8 degree Celsius.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- 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
Product temperature excursion issue
Symptomtext
Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival; Total duration of the excursion refrigerated temps for max of 4 hrs; They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge); This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) 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 (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Reporter stated that it was unknown if the vial undergone a previous temperature excursion. The storage condition at the time of the excursion was frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was partially thawed/liquid. The maximum or minimum temperature reached was 8 degrees Celsius. The total duration of the excursion refrigerated temperatures for max of 4 hours. The temperature fluctuations occurred as frozen-refrigerated and refrozen. And also stated that the vial was moved to the fridge on 06-Oct-2021 and administered post 30 days. No treatment information was provided. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. On 06-Oct-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C. 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
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- 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
Product temperature excursion issue
Symptomtext
Frozen vials, removed and transported at refrigerated temperature, re-frozen at the time of arrival; Total duration of the excursion refrigerated temps for maximum of 4 hours; They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge); This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temperature, re-frozen at the time of arrival), PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for maximum of 4 hours) and EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temperature, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for maximum of 4 hours). At the time of the report, PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temperature, re-frozen at the time of arrival), PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for maximum of 4 hours) and EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. It was reported that the vial was moved to fridge on 06-Oct-2021. The storage condition of the vial at the time of the excursion was frozen storage/refrigerated storage/ambient room temperature frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was reported as partially thawed/liquid. The maximum or minimum temperature reached by the vial was 8 degree Celsius. It was reported that the total duration of excursion at refrigerated temperature was for a maximum of 4 hours. It was reported that the vials were re-frozen. Temperature fluctuations had occurred from frozen state to refrigerated state to being re-frozen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.; Total duration of the excursion refrigerated temps for max of 4 hrs.; Accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs.) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. On 06-Oct-2021, vaccine was moved to fridge. It was reported that the vaccines were shipped in refrigerated temps and then re-frozen for storage once arriving the facility. The vaccine was partially thawed/liquid and underwent temperature excursion for maximum of 4 hours. 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
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) 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 (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) 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. Vials were moved to fridge on 06-Oct-2021. Treatment details was not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- 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
Product temperature excursion issue
Symptomtext
This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (Vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product information was not provided. It was reported that the vaccines were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. On 06-Oct-2021 vaccine was moved to fridge. The facility thought that the vials are received frozen from Moderna so they had unpacked them and put them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. Duration of the excursion Refrigerated temperature for maximum of 4 hours. Vaccine administered post 30 days from the initial storage at 2 degree C to 8 degree C. Treatment information was not provided. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. On 06-Oct-2021, vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C. Concomitant and treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided Treatment medication was not provided by the reporter The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. On 1-Dec-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- 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
Product temperature excursion issue
Symptomtext
Vials are received in refrigerated temperatures and not frozen; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; Accidentally administerred refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Accidentally administerred refrozen vials to their patients), PRODUCT STORAGE ERROR (Vials are received in refrigerated temperatures and not frozen) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Accidentally administerred refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vials are received in refrigerated temperatures and not frozen) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Accidentally administerred refrozen vials to their patients), PRODUCT STORAGE ERROR (Vials are received in refrigerated temperatures and not frozen) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported by reporter. Vial was moved to fridge on 06-Oct-2021. Both 5.5 ml and 7.5 ml vials were received in partially thawed/liquid condition. Maximum or minimum temperature reached was 8 degree Celsius. Total duration of excursion was 4hrs. No treatment medication was reported by reporter. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- 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
Product temperature excursion issue
Symptomtext
Frozen vials, removed and transported at refrigerated temperature, re-frozen at the time of arrival; Total duration of the excursion refrigerated temps for maximum of 4 hours; They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge); This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temperature, re-frozen at the time of arrival), PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for maximum of 4 hours) and EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) 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 (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temperature, re-frozen at the time of arrival) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for maximum of 4 hours). At the time of the report, PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temperature, re-frozen at the time of arrival), PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for maximum of 4 hours) and EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient Id was reported. No concomitant medications were reported. No treatment medications were reported. It was reported that the vial was moved to fridge on 06-Oct-2021. The storage condition of the vial at the time of the excursion was frozen storage/refrigerated storage/ambient room temperature frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was reported as partially thawed/liquid. The maximum or minimum temperature reached by the vial was 8 degree Celsius. It was reported that the total duration of excursion at refrigerated temperature was for a maximum of 4 hours. It was reported that the vials were re-frozen. Temperature fluctuations had occurred from frozen state to refrigerated state to being re-frozen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. On 06 Oct 2021, vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 8 degree Celsius, total duration of the excursion refrigerated temperature for maximum of 4 hours. The facility thought that the vials were received frozen from Moderna, so they have been unpacking them and putting them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. Treatment information was not reported. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) 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 (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient MRN id was reported as 531678. No concomitant medication was provided. It was unknown if the vial was undergone a previous temperature excursion. The storage condition at the time of the excursion was frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was partially thawed/liquid. The maximum temperature reached was 8?C. the total duration of the excursion refrigerated temps for max of 4 hours. The temperature fluctuations occurred as frozen-refrigerated and refrozen. On 06-OCT-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2 degree Celsius to 8 degree Celsius. Treatment medication was not provided by the reporter. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- 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
Product temperature excursion issue
Symptomtext
Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.Total duration of the excursion refrigerated temps for max of 4 hrs; Accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. On 06-Oct-2021, vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C. It was reported that the vaccines were shipped in refrigerated temps and then re-frozen for storage once arriving the facility. The vaccine was partially thawed/liquid and underwent temperature excursion for maximum of 4 hours. 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
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The concomitant medications on use were not provided. The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. On 06-Oct-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2 degree Celsius to 8 degree Celsius. The facility thought that the vials were received frozen from Moderna, so they have been unpacking them and putting them back into the facility freezer. They just recently found out that the vials were received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. No treatment information was provided. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported by reporter. The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. Further it was reported that vial was moved to fridge on 06-Oct-2021. Both 5.5 ml and 7.5 ml vials were received in partially thawed/liquid condition. Maximum or minimum temperature reached was 8 degree Celsius. Total duration of excursion was 4hrs. No treatment medication was reported by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) 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 (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) 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 provided. It was reported that the vaccines were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. On 06-Oct-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2 degree C to 8 degree C. The facility thought that the vials are received frozen from Moderna so they had unpacked them and put them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. No treatment medication were provided. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product storage error
Product temperature excursion issue
Symptomtext
Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) and POOR QUALITY PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) and PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) and POOR QUALITY PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Treatment information was not provided. The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrived at facility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 15.11.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Nov-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 (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided 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. Vials were moved to fridge on 06-Oct-2021. Treatment details was not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) 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 (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. It was unknown if the vial was undergone a previous temperature excursion. The storage condition at the time of the excursion was frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was partially thawed/liquid. The maximum temperature reached was 8?C. the total duration of the excursion refrigerated temps for max of 4 hours. The temperature fluctuations occurred as frozen-refrigerated and refrozen. On 06-OCT-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2 degree Celsius to 8 degree Celsius. Treatment medication was not provided by the reporter. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) 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 (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant information was reported. No Treatment information was reported. The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. On 06-Oct-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge); This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) 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 (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge)), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant Medications were provided by the Reporter No Treatment Medications were provided by the Reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; Accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Accidentally administering refrozen vials to their patients ), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Accidentally administering refrozen vials to their patients ). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Accidentally administering refrozen vials to their patients ), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medication reported. On 06-Oct-2021, vaccine was moved to fridge. It was reported that the vaccines were shipped in refrigerated temps and then re-frozen for storage once arriving the facility. The vaccine was partially thawed/liquid and underwent temperature excursion for maximum of 4 hours. No Treatment medication reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vial was moved to the fridge on 06 Oct 2021 and administered post 30 days from the initial storage at 2 degree Celsius to 8 degree Celsius. The facility thought that the vials were received frozen from Moderna, so they have been unpacking them and putting them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. No treatment information was reported. This case was linked to MOD-2022-496015, MOD-2022-501580.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.03.2022
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported.On 08-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) 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 information was not provided. Treatment information was not provided. PAT_MRN_ID: 01767194 The vials were frozen, sipped in refrigerated temperature and then refrozen for storage once arrive at facility. On 06-Oct-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.03.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient MRN ID reported. Concomitant products were not provided. On 06 Oct 2021, vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 8 degree Celsius, total duration of the excursion refrigerated temperature for maximum of 4 hours. The facility thought that the vials were received frozen from Moderna, so they have been unpacking them and putting them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. Treatment medications were not reported. This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.03.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product information was not provided Total duration of the excursion refrigerated temperature for maximum of 4 hour. On 06-Oct-2021, Vial was moved to fridge. The facility thought that the vials are received frozen from Moderna so they had unpacked them and put them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. Vaccine administered post 30 days from the initial storage at 2 degree C to 8 degree C 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
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.03.2022
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival; Patients were administered refrozen vials; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients were administered refrozen vials), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) 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 (Patients were administered refrozen vials). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients were administered refrozen vials), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient MRN ID was 07858380. Concomitant medication list was not provided. The vials were frozen, shipped in refrigerated temperature and then refrozen for storage once arrive at facility. Further it was reported that vial was moved to fridge on 06-Oct-2021. Both 5.5 ml and 7.5 ml vials were received in partially thawed/liquid condition. Maximum or minimum temperature reached was 8 degree Celsius. Total duration of excursion was 4hrs. 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
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. On 06-Oct-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C. 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
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.03.2022
- Impfdatum
- 10.11.2021
- Beginn
- 10.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) 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. Vials were moved to fridge on 06-Oct-2021. Treatment details was not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.03.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product information was not provided Total duration of the excursion refrigerated temperature for maximum of 4 hour. On 06Oct2021, Vial was moved to fridge. The facility thought that the vials are received frozen from Moderna so they had unpacked them and put them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. Vaccine administered post 30 days from the initial storage at 2 degree C to 8 degree C Treatment information was not provided This case was linked to MOD-2022-496015 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.03.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- 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
Product temperature excursion issue
Symptomtext
They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrived at facility. On 06-Oct-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C. 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
- AL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 28.09.2021
- Beginn
- 02.10.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Alopecia
Blood test
Symptomtext
Hair loss....my hair has never come out I've had blood work drawn and do not have an auto immune disorder or any previous health conditions. My hair started falling out right after the shot and has progressively gotten worst. I now have 11 bald spots and am shedding all over as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alopecia
- Hospital-Tage
- -
- Labordaten
- 10/1102021 Blood work
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Suboxone
- Allergien
- Penacillin, levaquin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 18.02.2022
- Impfdatum
- 28.10.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 60,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
COVID-19 test in triage returned positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 10.03.2021
- Beginn
- 18.01.2022
- Tage bis Beginn
- 314,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Vaccine breakthrough infection
Symptomtext
Hospitalized for a Breakthrough COVID infection in patient who received the primary 2 shot series and a booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- COPD; Diabetes; hypertension; asthma; Sleep Apnea; hypercholesterolemia; neuropathy
- Vorgeschichte
- COPD; Diabetes; hypertension; asthma; Sleep Apnea; hypercholesterolemia; neuropathy
- Andere Medikamente
- Atorvastatin; diltiazem; gabapentin; glipizide; meclizine; meloxicam; metformin; Ramipril; triamterene/hydrochlorothiazide
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 28.10.2021
- Beginn
- 26.01.2022
- Tage bis Beginn
- 90,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccine breakthrough infection
Symptomtext
Hospitalized with breakthrough COVID infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 22.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 5,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Audiogram abnormal
Deafness neurosensory
Deafness unilateral
Sudden hearing loss
Symptomtext
Diagnosed with sudden onset SNHL 5 days after Moderna Booster shot. Drastic hearing loss in Rt. EAR. Treatment was high-dose steroid taper starting at 60 mg down to 10mg over the course of 14 days. After treatment hearing improved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Audiogram abnormal
- Hospital-Tage
- -
- Labordaten
- Audiogram at visit to LVPG Ear, nose and throat On Nov 1 2021 showed significant neuro sensory ASYMMETRY.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 15.10.2021
- Beginn
- 13.01.2022
- Tage bis Beginn
- 90,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Symptomtext
hospitalization with covid after being fully vaccinated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 1/13/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- DMII
- Andere Medikamente
- unknown
- Allergien
- amoxicillin, clavulanic acid
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 26.10.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 73,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asymptomatic COVID-19
SARS-CoV-2 test positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- PCR 1/7/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Multiple Sclerosis
- Andere Medikamente
- Acetyl L-Carnitine Alpha-Lipoic Acid, Asprin-Childrens, Aubagio , B Complex Vitamins, Coenzyme Q-10, Fish Oil, Multi Vitamin, Vitamin D3.
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 03.09.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 32,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anaemia
Biopsy endometrium normal
Blood test abnormal
Contraception
Endometrial thickening
Laboratory test
Postmenopausal haemorrhage
Ultrasound uterus abnormal
Symptomtext
I started bleeding 10/5/21; I am POST menopausal. I had severe bleeding with massive clots. I went to Dr 10/19/21 to stop bleeding. Dr put me on Progestrone to stop it. It stopped for 24 hrs then back heavy again. Oct 26 was put on birth control pills to stop bleeding. Which it did. Preventative cancer screening took place. My uterus had a thickened endometrial lining (16mm) diagnosed via ultrasound. Had to have a VERY painful endometrial biopsy which was cancer negative. I lost so much blood I had blood test and it came back I'm anemic (due to blood loss). I had more labs which came back as I am absolutely diagnosed POST menopausal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaemia
- Hospital-Tage
- -
- Labordaten
- labs ultrasound 11/17/21 painful endometrial biopsy of my uterus (through my cervix) labs again
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Graves (in remission)
- Andere Medikamente
- muti vitamins, 2 mg methimazole, lovastatin 15 mg
- Allergien
- bee stings
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Acoustic stimulation tests abnormal
Deafness unilateral
Ear discomfort
Ear infection
Tympanic membrane perforation
Symptomtext
Right ear hearing loss. Originally thought ear infection-felt like under water or ear clogged. No other symptoms, so didn't seek treatment right away. Put ear pods in & couldn't hear in right ear. Went to primary care physician & started on antibiotic & steroids on 12/17/21. No improvement went to ENT on 12/23-said no infection/fluid/or obstruction. Hearing test showed hearing loss. Punctured ear drum & loaded in steroids. Started on high dose steroids for 16 days. Outcome to be determined still.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests abnormal
- Hospital-Tage
- -
- Labordaten
- 12/23/21: Hearing test-showed hearing loss
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroid
- Andere Medikamente
- Synthroid 100 mcg/day
- Allergien
- NA
- Vorherige Impfungen
- Post Moderna shot #2: calcific tendonitis of left shoulder 4/2021, 48 years old
- Staat
- IL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 29.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blepharospasm
Discomfort
Facial discomfort
Laboratory test normal
Sensory disturbance
Stress
Symptomtext
A few weeks after my injection I started developing a heaviness in my Left temporal forehead and cheek area. Developed a twitching in my left eye. And it seems to be along the branch of a facial nerve in my left side. I don't have muscle weakness or dropping just heaviness and change in sensation on the left side of my face down to my left cheek area. I saw my doctor and I have been under a great deal of stress lately and she put me on a low mg dose of Celexa. I have an MRI scheduled to rule out any other problems other than stress. 2.5 weeks prior to vaccine I had Botox on my forehead. And I've had it before without any complications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blepharospasm
- Hospital-Tage
- -
- Labordaten
- I had routine lab work, everything was normal.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- I have esophageal reflux; arthritis in my bones; total knee replacements; hypothyroidism; high blood pressure
- Andere Medikamente
- Omasar; Hydrochlorothiazide; Estradiol; Pantoprazole; Zolpidem; Aspirin; Fish oil; CoQ10; Citracal +Vitamin D;, Mira LAX; Centrum Silver; Vitamin D
- Allergien
- I'm allergic to antibiotic Timenton
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysmenorrhoea
Heavy menstrual bleeding
Symptomtext
Patients reports extremely heavy menstrual bleeding with slight pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysmenorrhoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 10.11.2021
- Impfdatum
- 16.09.2021
- Beginn
- 16.09.2021
- 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
12 year old was administered the first dose of the Moderna Covid19 Vaccine.; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (12 year old was administered the first dose of the Moderna Covid19 Vaccine.) in a 12-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. Concomitant products included CETIRIZINE and HYDROXYZINE for an unknown indication. On 16-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Sep-2021, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (12 year old was administered the first dose of the Moderna Covid19 Vaccine.). On 16-Sep-2021, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (12 year old was administered the first dose of the Moderna Covid19 Vaccine.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Treatment information was reported. This is a case of Product administered to patient of inappropriate age for this 12-year-old male patient with no relevant medical history reported. The patient received the first dose of mRNA-1273 vaccine on 16-Sep-2021. No adverse events were reported. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This is a case of Product administered to patient of inappropriate age for this 12-year-old male patient with no relevant medical history reported. The patient received the first dose of mRNA-1273 vaccine on 16-Sep-2021. No adverse events were reported. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- CETIRIZINE; HYDROXYZINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
No adverse event
Symptomtext
resident received a dose of pfizer on 10/20/21 resident had previously been vaccinated with J&J 4/6/21. On 11/4/21 received a booster dose . no adverse reactions to extra dose was seen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- UNSPECIFIED DEMENTIA WITH BEHAVIORAL DISTURBANCE, POLYOSTEOARTHRITIS, ESSENTIAL (PRIMARY) HYPERTENSION, OTHER SPECIFIED DISORDERS OF BONE DENSITY AND STRUCTURE, DYSPHAGIA, OROPHARYNGEAL PHASE, IRON DEFICIENCY ANEMIA, MUSCLE WEAKNESS , DISORDER OF BILIRUBIN METABOLISM,
- Andere Medikamente
- protonix, Ferrous Sulfate, Vitamin B12 Tablet 500 MCG, Mirtazapine ,risperiDONE, Norvasc
- Allergien
- penicillins
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong patient
Symptomtext
Error: Wrong Patient (documentation in EMR)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong patient
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
Pt presented to clinic to start Moderna vaccine series. Pt did not disclose that she had originally started the Pfizer vaccine series in February and had received one dose at that time. Pt given first dose of Moderna vaccine. When pt presented for second dose of Moderna vaccine, the original Pfizer vaccine was discovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Tinnitus
Symptomtext
Tinnitus in left ear, started on Weds 10/27/21, tinnitus is constant in left ear
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- Hearing test 11/2/21
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic back pain
- Andere Medikamente
- Unisom 25mg at bedtime, Celecoxib 400mg at bedtime
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- 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
10 patients received expired dose; 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 (10 patients received expired dose) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (10 patients received expired dose). At the time of the report, EXPIRED PRODUCT ADMINISTERED (10 patients received expired dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), 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.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect route of product administration
Symptomtext
Error: Wrong Route (SC, IM, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
claim #2155603, 2155604, 2155606, 2155607, 2155609, 2155610, 2155612, 2155613, 2155614, 2155615 Moderna dose given on 10-25-21 had expired on 10/22/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- unkown
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- unknown
- Andere Medikamente
- simvastatin,levothyroxine
- Allergien
- pennicillin`
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heavy menstrual bleeding
Hypomenorrhoea
Symptomtext
Pt. states that after receiving the 1st dose of Moderna 10/01/2021, started experiencing symptoms 10/06/2021 of continuous menstrual (changes light/heavy). Gynecologist visit 10/26/2021 recommendations of Observation. Still continuing to experience symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heavy menstrual bleeding
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Low Low Estrin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 20.10.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Electrocardiogram normal
Urine analysis
Vaccine positive rechallenge
Symptomtext
Within 10 minutes, I had severe headache again (same as after the 1st Moderna COVID-19 vaccine) and within 30 minutes, I had dizziness and the dizziness is still present a week later. The chills have been ongoing since the first vaccine. I'm still cold all the time. The numbness in my leg and heel was getting better, and now it has gotten worse after getting the second dose. My fingers on left hand go numb from time to time. I have heart palpitations at time. I talked to my PCP last Friday, and he said to wait it out through the weekend. I called him on Monday, and yesterday; I saw him, and he did EKG that came back normal. He ran blood tests and urine and I'm still waiting to hear back from him to hear about those results. I have been taking Motrin or Tylenol for body aches and headaches. Those symptoms seem to be better now. Now, it's just the dizziness and the numbness in my leg, and heel, and fingers. The dizziness comes and goes. I haven't tried to drive or gone to work since the vaccine. I'm a dentist and I can't have a dizzy spell come over me when I am working on a patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- Doctor- EKG- Normal- 10/26 Normal- Blood and Urine- 10/26
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Lisinopril 10mg 1X Per Day Multivitamin
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.09.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Pfizer COVID19 Vaccine was administered; This spontaneous case was reported by a nurse and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Pfizer COVID19 Vaccine was administered) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. Previously administered products included for COVID-19 vaccination: Pfizer COVID-19 Vaccine on 18-Sep-2021. On 18-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Sep-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Pfizer COVID19 Vaccine was administered). On 18-Sep-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Pfizer COVID19 Vaccine was administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant drugs were not reported. Treatment medications were not provided. Most recent FOLLOW-UP information incorporated above includes: On 19-Oct-2021: Reporter information, contact details were Updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 23.10.2021
- Impfdatum
- 16.10.2021
- Beginn
- 16.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 23.10.2021
- Impfdatum
- 16.10.2021
- Beginn
- 16.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 23.10.2021
- Impfdatum
- 16.10.2021
- Beginn
- 16.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 20.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine administered from a vial greater than 12 hours post-puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT STORAGE ERROR (Vaccine administered from a vial greater than 12 hours post-puncture) in a 29-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. Concomitant products included ETHINYLESTRADIOL, NORGESTIMATE (SPRINTEC) for Birth control. On 12-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Oct-2021, the patient experienced PRODUCT STORAGE ERROR (Vaccine administered from a vial greater than 12 hours post-puncture). On 12-Oct-2021, PRODUCT STORAGE ERROR (Vaccine administered from a vial greater than 12 hours post-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. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- SPRINTEC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 20.10.2021
- Impfdatum
- 11.10.2021
- Beginn
- 11.10.2021
- 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
Product storage error
Symptomtext
Dose administered >12 hours post puncture; stored at room temperature beyond 12 hours; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered >12 hours post puncture) and PRODUCT STORAGE ERROR (stored at room temperature beyond 12 hours) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered >12 hours post puncture) and PRODUCT STORAGE ERROR (stored at room temperature beyond 12 hours). On 11-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Dose administered >12 hours post puncture) and PRODUCT STORAGE ERROR (stored at room temperature beyond 12 hours) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. patients received the second dose of Moderna COVID-19 vaccine from a vial that was punctured and stored at room temperature beyond 12 hours. no of vials is given as 1 , vial was initially stored in the refrigerator 2-oct-2021,first punctured on 10-oct-2021,administered on 11-oct-2021 at noon. Total amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F): 30 hours. no concomitant and treatment medications are provided by the reporter. This case was linked to MOD-2021-348346 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 19.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Incorrect administration as Moderna is not indicted under 18 yo.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Loratadine 10mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 19.10.2021
- Impfdatum
- 11.10.2021
- Beginn
- 11.10.2021
- 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
Product storage error
Symptomtext
Dose administered >12 hours post puncture; Dose administered from a vial that was punctured and stored at room temperature beyond 12 hours; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered >12 hours post puncture) and PRODUCT STORAGE ERROR (Dose administered from a vial that was punctured and stored at room temperature beyond 12 hours) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 061E21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Oct-2021 at 12:00 PM, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Oct-2021, the patient experienced PRODUCT STORAGE ERROR (Dose administered from a vial that was punctured and stored at room temperature beyond 12 hours). On 11-Oct-2021 at 12:00 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered >12 hours post puncture). On 11-Oct-2021, PRODUCT STORAGE ERROR (Dose administered from a vial that was punctured and stored at room temperature beyond 12 hours) had resolved. On 11-Oct-2021 at 12:00 PM, EXPIRED PRODUCT ADMINISTERED (Dose administered >12 hours post puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that the vial was initially stored in refrigerator on 02-Oct-2021 and the vial was first punctured on 10-Oct-2021. Post puncture vial was stored in room temperature for 30 hours. No concomitant medication was reported. No treatment information was reported. This case was linked to MOD-2021-348407 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 18.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Interchange of vaccine products
No adverse event
Symptomtext
Patient received an expired Dose of Pfizer vaccine on 9/2021 at pharmacy. Per patient she was told that she will need to get Covid vaccine as she received an expired dose at their facility. Patient received a Moderna vaccine on 10/18/2021.No adverse reactions reported by patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 15.10.2021
- Impfdatum
- 15.10.2021
- Beginn
- 15.10.2021
- 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
No adverse event
Symptomtext
Patient thought they received Moderna previously, documented that on pre-vaccine checklist, and scheduled today for second dose Moderna, Denied having vaccine card, received Moderna vaccine, then returned with vaccine card after visit, nurse noted patient previously received Pfizer not Moderna. Nursing administrator notified, NA notified clinical director for guidance. Although, mixed-series doses is not considered approved per the EUA and the CDC has specific guidance for exceptional circumstances to interchange them, it is still an error; however, per the CDC "Do not repeat dose". Patient notified of error, encouraged to report any unexpected side effects / adverse effects ASAP to clinic and follow up with provider if needed, if emergent sx arise notify 911/EMS. Patient verbalized understanding and agreement. No s/sx adverse effects noted thus far.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 15.10.2021
- Impfdatum
- 14.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Postmenopausal haemorrhage
Symptomtext
Vaginal bleeding post menopause.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Postmenopausal haemorrhage
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Levothyroxine, Progesterone, Estradiol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 13.10.2021
- Impfdatum
- 18.08.2021
- Beginn
- 25.08.2021
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- F
- 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
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 09.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 09.10.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mass
Symptomtext
The morning after receiving the first vaccination dose, a small (almost 1 cm) hard, non-tender, immobile lump appeared on the right-outer area of my hard palate. It has been 8 days and the lump is still present; however, it is smaller in size. To be seen by my ENT for follow-up if lump remains persistent after 2 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mass
- Hospital-Tage
- -
- Labordaten
- n/a at the moment
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Fibroadenoma of breast
- Andere Medikamente
- Liposomal Glutathione, Pre-natal, Probiotic
- Allergien
- Aplisol PPD (mild reaction)
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 08.10.2021
- Impfdatum
- 27.09.2021
- Beginn
- 27.09.2021
- 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
patient received 3rd dose of Moderna on 9/27/21 - dose #1 was given 3/25/2021 - dose #2 was given 04/20/2021 - patient is not immune compromised so did not qualify for an additional dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 02.10.2021
- Impfdatum
- 24.09.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Lymphadenopathy
Symptomtext
Patient experienced an enlargement of lymph nodes located on left upper body, particularly the neck and axillary closest to injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 02.10.2021
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Symptomtext
Systemic: numbness-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 01.10.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Gave a booster dose when not indicated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 01.10.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
not in CDC guidlines
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- Cancer
- Vorgeschichte
- Cancer
- Andere Medikamente
- Zofran, Compazine, Lidocaine oral rinse, Radiation,
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 30.09.2021
- Impfdatum
- 25.09.2021
- Beginn
- 25.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient received third dose (booster shot) for Moderna. Patient did not qualify for booster dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 27.09.2021
- Beginn
- 27.09.2021
- 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
Patient was given a booster dose that was not eligible and outside of the guidelines
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 27.09.2021
- Beginn
- 27.09.2021
- 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
patient recevied the booster for moderna which patients doesnt qualify for yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 27.09.2021
- Beginn
- 27.09.2021
- 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
Patient recevied a booster dose which patient doesnt qualify .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 29.09.2021
- Impfdatum
- 28.09.2021
- Beginn
- 28.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
DOSE GIVEN TOO EARLY. PT CAME IN SAYING IT WAS FOR HIS SECOND DOSE BUT HE HAD ALREADY COMPLETED A DOSE OF PFIZER? OUR SYSTEM WAS UNABLE TO CATCH THE PREVIOUS COMPLETED PFIZER VACCINE SERIES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- NO ADVERSE EVENTS SO FAR
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 28.09.2021
- Impfdatum
- 25.09.2021
- Beginn
- 25.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Interchange of vaccine products
No adverse event
Symptomtext
Was given the incorrect vaccination. Went to get a booster vaccine and was given this by pharmacist. No possible side effects as of now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Doesn't have a spleen High Blood Pressure High Cholestorol
- Andere Medikamente
- Multi Vitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 27.09.2021
- Impfdatum
- 25.09.2021
- Beginn
- 25.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Symptomtext
Systemic: Numbness (specify: facial area, extremities)-Medium, Additional Details: numbness in middle and ring finger on left arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 26.09.2021
- Beginn
- 26.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 23.09.2021
- Impfdatum
- 23.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Interchange of vaccine products
Wrong product administered
Symptomtext
patient was supposed to get flu vaccine but was inadvertently given moderna(covid) vaccine. Patient stated that he got 2 doses of Pfizer vaccine; Last dose he got in February of this year. Consequently pharmacist gave him the fluzone HD which he really wanted, Patient was not upset or worried. Rph explained that both pfizer and moderna come from Mrna sources. and remember not to get the third booster for pfizer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- leukemia
- Vorgeschichte
- leukemia
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 22.09.2021
- Impfdatum
- 04.09.2021
- Beginn
- 19.09.2021
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood urine present
International normalised ratio increased
Symptomtext
INR went very high. 5.6 and Warfarin dose had to be suspended for two days. I also started to have blood in my urine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood urine present
- Hospital-Tage
- -
- Labordaten
- INR home test
- Aktuelle Erkrankungen
- Rheumatoid Arthritis Congenital Heart Defect
- Vorgeschichte
- Rheumatoid Arthritis Congenital Heart Defect
- Andere Medikamente
- Metoprolol Warfarin Losarten Zetia Folic acid Aspirin Folic acid Biotin
- Allergien
- Iodine dye
- Vorherige Impfungen
- -