VAERS Reports #211A21A

VAERS 2504327

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

kritisch

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 24.09.2021
Beginn: 12.10.2022
Tage bis Beginn: 383,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute left ventricular failure Acute respiratory failure Aortic dilatation Atrial fibrillation CHA2DS2-VASc-score COVID-19 pneumonia Cardiac failure Cardiac failure congestive Chest X-ray abnormal Culture positive Diuretic therapy Dyspnoea Echocardiogram abnormal Ejection fraction normal Fluid intake restriction Hyperlipidaemia Hypertension Incentive spirometry

Symptomtext

COVID-19 pneumonia Acute hypoxic respiratory failure secondary to COVID-pneumonia and acute congestive heart failure Presenting with bilateral opacities on chest x-ray, symptom onset 2 weeks prior to admission (9/27/22). No previous confirmed diagnosis and was vaccinated originally with Johnson & Johnson vaccine, no follow-up boosters. Infectious disease consulted currently on IV remdesivir, dexamethasone, Tocilizumab Tocilizumab started 10/16/2022 Initially requiring BiPAP then heated high flow oxygen then currently oxygen saturation maintained on 3 L of oxygen through nasal cannula. Wean as tolerated. Incentive spirometry. Permanent atrial fibrillation Home medication include carvedilol 25 mg twice daily and digoxin 0.125 mg daily Currently rate controlled on digoxin 0.125 mg daily and low-dose carvedilol 6.25 mg twice daily CHA2DS2-VASc score 2 Coumadin pharmacy to dose, INR 2.4. Acute congestive heart failure likely right-sided heart failure Acute diastolic congestive heart failure Cardiac diet Salt and fluid restriction Daily I's and O's and body weight IV then p.o. diuretics Heart failure education Echocardiogram 10/14/2022 showed EF 55% RV dilated with dilated aortic root 4.3 cm Streptococcus salivarius bacteremia (1 out of 2 cultures) 10/12/2022 Repeat cultures negative Likely contaminant, status post discontinue ceftriaxone Hypertension Home meds include lisinopril 2.5 mg daily and Coreg 25 mg twice daily initially on hold due to borderline hypotension. Currently on lisinopril 2.5 mg daily and Coreg 6.25 mg twice daily. Hyperlipidemia On statin therapy History of coronary artery disease Nonobstructive coronary artery disease based on cardiac cath in 2011 Guideline directed medical therapy. Morbid obesity Body mass index 48.9 Encourage weight loss and lifestyle modification Obstructive sleep apnea BIPAP nightly. Outpatient sleep study and follow-up with sleep medicine as an outpatient. Chronic lymphedema and scaling lower extremity Topical Vaseline lower extremity. Patient denied any dressings. Chronic thrombocytopenia Platelet count stable. ~80-100 We discharge patient home after improvement of general condition and shortness of breath. Patient to follow-up with PCP in 1 week. Follow-up with pulmonary/sleep medicine and ID as noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2207373

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

kritisch

Staat: WA
Alter: 53,0
Geschlecht: M
Eingang: 30.03.2022
Impfdatum: 04.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Balance disorder Blood pressure decreased Cardiac disorder Computerised tomogram normal Electrocardiogram abnormal Fall Gait inability Loss of consciousness Magnetic resonance imaging head normal Myocardial infarction Nausea Neurological symptom Pain Tachycardia X-ray normal

Symptomtext

Loss of balance, nausea, falling on Tue Oct 5 most of the day. Resumed on Wed Oct 6 to a point when I was unable to walk upright at home (falling) thus went to Urgent Care with these "stroke like symptoms" and they sent me down to ER. Cat/MRI/Xray from neck up but no signs of stroke. Was given Meclizine. After 4 hours symptoms improved. 6 weeks later I had what I assume was a massive clot in right thigh inside. Violent paint and passed out at home. After 30 min was able to pull myself together and BP dropped a little. Did not go to hospital due to cost from first visit. After this point (Nov) I developed chronic heart and blood pressure issues (tachycardia and 160/100 bp). Later EKG late Jan 2022 at Primary Care in Jan suggested "inferior infarct" and I was referred to cardiologist. Have been working with Cardiology since Mar 2022 for further diagnostics. Have been working on general health on my own. Now 6 months later BP is down to normal again but sleep heart rate is still never go below 67 bpm, but much better than 95 which I had from Dec 2021-Feb 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: None
Allergien: -
Vorherige Impfungen: 2005 got several vaccines duing immegration and was very sick for months. Don't have details/logs on that.

VAERS 2119278

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

kritisch

Staat: TN
Alter: 73,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 02.11.2021
Beginn: 26.01.2022
Tage bis Beginn: 85,0
Dosis: 1
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Fully vaccinated with Janseen x1. Tested positive for Covid on 01/26/2022. Admitted to Medical Center on 01/26/2022. Expired on 02/01/2022 while still hospitalized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1966601

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

kritisch

Staat: PA
Alter: 43,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: -
Beginn: 09.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Blood test Cerebrovascular accident Chest X-ray Computerised tomogram head Computerised tomogram neck Echocardiogram Magnetic resonance imaging head

Symptomtext

STROKE AFTER RECEIVING JANSSEN COVID-19 VACCINE BOOSTER DOSE; This spontaneous report received from a patient concerned a 43 year old female. Initial information processed with additional information received from reporter on 15-DEC-2021. The patient's height was 177.8 cm, and weight were not reported. The patient's concurrent conditions included: environmental allergy, non alcoholic, birth control, and non smoker, and other pre-existing medical conditions included: The patient had no known medical condition and no known drug allergies. The patient did not have any drug abuse/illicit drug use. The patient did not have any other medical history or relevant pre-existing condition. Patient had no illness at time of vaccination. Patient had no history of similar event. Patient had no history of any allergy to vaccine, drug, or food. Patient had no pre-existing acute illness 30 days prior to vaccination. Patient had no history of hospitalization in last 30days, with cause. Patient had no family history of any disease (relevant to vaccination) or allergy. The patient was not not pregnant or breastfeeding at the time of reporting. The patient did not have COVID-19 infection. The patient experienced flu like symptoms, fever, chills, achiness (Dose number in series 1) when received covid-19 vaccine ad26. cov2. s (suspension for injection, route of admin not reported, batch number: 205A21A, expiry: unknown) dose was not reported, 1 total, administered on 12-APR-2021 for prophylactic vaccination (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A, expiry: 14-DEC-2021, (Gauge/length of the needle: 23 g, 0.6 mm*25 mm, Temperature 38-41 F)) 0.5 ml, 1 total, administered on 08-Dec-2021;12:00 to right arm for prophylactic vaccination (Dose number in series 2). No issue related to the storage of the vaccine. Concomitant medications included montelukast sodium for allergies, levocetirizine dihydrochloride for allergies, and drospirenone/ethinylestradiol betadex clathrate for birth control. On 08-DEC-2021, immediately after she received the booster dose, she felt a tingling sensation in her mouth and that her mouth went numb. At that time the nurse practitioner given diphenhydramine hydrochloride (benadryl) and lansoprazole (prevacid) and that afterwards nothing happened. The patient passed the phone to other person to complete her report stating previously that she just had a stroke (Dose number in series 2) and so may not be able to complete the call. Reporter stated that, On 09-DEC-2021, around 09:00 to 10:00 A.M, at work the patient started to feel that her vision went blank, her arm started to tingle, she could not make words and so she went to the health facility. At the hospital, she was given the standard of care including an Chest X-ray, Computerised tomogram head and neck, Echocardiogram, MRI brain (Magnetic resonance imaging) and blood work and then was administered Tissue plasminogen activator (TPA) alteplase. Patient visited the emergency room. Patient was stayed in the hospital for a total of about 24 hours was discharged on 10-DEC-2021 with prescriptions for clopidogrel and lipitor. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from tingling sensation in her mouth/arm started to tingle/face tingled, and stroke after receiving Janssen covid-19 vaccine booster dose This report was serious (Hospitalization Caused / Prolonged). This case, involving the same patient is linked to 20211228737.; Sender's Comments: V0:20211229198-COVID-19 VACCINE AD26.COV2.S-Stroke after receiving Janssen covid-19 vaccine booster dose. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: Test Date: 20211209; Test Name: MRI brain; Result Unstructured Data: Not reported; Test Date: 20211209; Test Name: Computerised tomogram head; Result Unstructured Data: Not reported; Test Date: 20211209; Test Name: Computerised tomogram neck; Result Unstructured Data: Not reported; Test Date: 20211209; Test Name: Chest X-ray; Result Unstructured Data: Not reported; Test Date: 20211209; Test Name: Echocardiogram; Result Unstructured Data: Not reported; Test Date: 20211209; Test Name: Blood test; Result Unstructured Data: Not reported
Aktuelle Erkrankungen: Abstains from alcohol; Birth control; Environmental allergy; Non-smoker
Vorgeschichte: Comments: The patient had no known medical condition and no known drug allergies. The patient did not have any drug abuse/illicit drug use. The patient did not have any other medical history or relevant pre-existing condition. Patient had no illness at time of vaccination. Patient had no history of similar event. Patient had no history of any allergy to vaccine, drug, or food. Patient had no pre-existing acute illness 30 days prior to vaccination. Patient had no history of hospitalization in last 30days, with cause. Patient had no family history of any disease (relevant to vaccination) or allergy. The patient was not breastfeeding at the time of reporting. The patient did not have COVID-19 infection.
Andere Medikamente: YAZZ; SINGULAIR; XYZAL
Allergien: -
Vorherige Impfungen: -

VAERS 1936331

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

kritisch

Staat: OH
Alter: 83,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 09.03.2021
Beginn: 13.11.2021
Tage bis Beginn: 249,0
Dosis: 2
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death SARS-CoV-2 RNA

Symptomtext

2019 Novel Coronavirus RNA detected 11/17/1021 Hospitalized 11/17/2021 Patient died

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular disease
Andere Medikamente: -
Allergien: Allergic Morphine
Vorherige Impfungen: -

VAERS 1850722

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

kritisch

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: -
Beginn: 27.09.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abortion spontaneous Amniocentesis Chromosome analysis normal Exposure during pregnancy Foetal death Ultrasound scan Ultrasound antenatal screen abnormal Uterine dilation and curettage

Symptomtext

SPONTANEOUS ABORTION; VACCINE EXPOSURE DURING PREGNANCY; This spontaneous pregnancy report received from a physician concerned a 40 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. It was not reported whether the patient had been pregnant before. The patient received Covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: unknown, expiry: unknown) dose was not reported, frequency time 1 total was administered on 27-SEP-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 27-SEP-2021, the patient was vaccinated with Janssen Covid-19 vaccine resulting in vaccine exposure during pregnancy. The date of the patient's last menstrual period and expected delivery date were not reported. Before receiving the vaccine the patient had ultra sound and genetic testing which was normal. On 01-OCT-2021, patient had another ultrasound test and it was normal. On 18-OCT-2021, the patient was 14 weeks and 6 days pregnant and she had an ultra sound test that showed that the baby passed away (fetal demise). On 18-OCT-2021, the pregnancy resulted in a spontaneous abortion. On 21-OCT-2021, she had genetic test again and which was normal. The action taken with Covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the spontaneous abortion and vaccine exposure during pregnancy was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20211114914-COVID-19 VACCINE AD26.COV2.S-spontaneous abortion. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: MEDICAL HISTORY 20211114914-COVID-19 VACCINE AD26.COV2.S-vaccine exposure during pregnancy . This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Foetal death
Hospital-Tage: -
Labordaten: Test Date: 20211001; Test Name: Diagnostic ultrasound; Result Unstructured Data: Normal; Test Date: 20211018; Test Name: Diagnostic ultrasound; Result Unstructured Data: Fetal demise; Comments: Ultra sound that showed that the baby passed away (fetal demise); Test Name: Diagnostic ultrasound; Result Unstructured Data: Normal
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1861603

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

kritisch

Staat: CA
Alter: 66,0
Geschlecht: M
Eingang: 11.11.2021
Impfdatum: 30.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Aphasia Blood test Cerebrovascular accident Chest X-ray Computerised tomogram head abnormal Computerised tomogram neck Electrocardiogram Magnetic resonance imaging head abnormal Reading disorder

Symptomtext

On 11/5/2021 around 11AM I has trying to read and couldn't say anything correctly. Later in the day. I was talking to someone who told me I didn't sound right. He took me to the ER and they diagnosed me with a stroke. They did a bunch of testing including an MRI. blood work, EKG, chest XR, ECG, brain/head/neck CT. I was in the hospital from Friday night 11/5 to Sunday evening 11/7. That's the best I can remember.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: brain CT 11/5/2021, abnormal; Neck/head CT; Blood work 11/5/2021; MRI 11/5/2021, stroke; EKG 11/5/2021; ECG 11/5/2021; Chest XR.
Aktuelle Erkrankungen: None.
Vorgeschichte: Type 2 diabetes.
Andere Medikamente: Eliquis; Metoprolol; Sotalol; Atorvastatin; Glipizide; Metformin; Losartan.
Allergien: Xarelto.
Vorherige Impfungen: -

VAERS 1861362

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

kritisch

Staat: CO
Alter: 51,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 01.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute respiratory failure C-reactive protein increased COVID-19 Chest X-ray abnormal Fibrin D dimer increased Lung hypoinflation Lung opacity SARS-CoV-2 test positive

Symptomtext

Janssen COVID-19 Vaccine EUA: patient currently hospitalized for COVID-19 disease with acute hypoxemic respiratory failure. Receiving steroids, remdesivir, and oxygen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: SARS-CoV-2: positive Peak D-dimer to date: 380 ng/mL Peak CRP to date: 35.4 mg/L Chest x-ray: normal cardiac silhouette, mildly hypoexpanded lungs with faint bibasilar opacities; infection cannot be excluded
Aktuelle Erkrankungen: community acquired pneumonia, syncope, hypoglycemia, fall
Vorgeschichte: anemia, cancer, CHF, CKD, diabetes mellitus, dyspnea on exertion, GERD, hyperlipidemia, hypertension, neuropathy, oxygen dependent, seizures, OSA
Andere Medikamente: amlodipine, atorvastatin, diclofenac gel, Trulicity, Jardance, vitamin D2, furosemide, gabapentin, insulin, lidocaine patch, losartan, melatonin, nystatin, ofloxacin, Mirlax, Pred Forte, topiramate
Allergien: ondansetron
Vorherige Impfungen: -

VAERS 1856589

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

kritisch

Staat: WA
Alter: -
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: -
Beginn: 24.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Blood test Cerebrovascular accident Computerised tomogram Magnetic resonance imaging Neurological examination

Symptomtext

STROKE; This spontaneous report received from a patient concerned a maleof an unspecified age. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, 1 total, administered at right arm on 23-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 24-OCT-2021, the patient experienced general off feeling, headache and weakness were reported. On 25-OCT-2021, the patient started to feel partial paralysis in the right hand and leg and he went to work for a few hours and was sent home by employer. On 26-OCT-2021, the patient visited emergency room due to persistence of symptoms and he underwent through laboratory tests included blood tests, assessments for strength and motor skills and CAT (computerized axial tomography) scan performed results were not reported and he was admitted to the hospital along with this an MRI (magnetic resonance imaging) was performed. The next day, 27-OCT-2021, he got confirmation of a stroke had occurred. On 30-OCT-2021, the patient was discharged from the hospital. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered stroke. This report was serious (Hospitalization Caused / Prolonged).; Sender's Comments: V0: 20211106356-COVID-19 VACCINE AD26.COV2.S-stroke. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 5,0
Labordaten: Test Date: 20211026; Test Name: Blood test; Result Unstructured Data: unknown; Test Date: 20211026; Test Name: MRI; Result Unstructured Data: unknown; Test Date: 20211026; Test Name: CAT scan; Result Unstructured Data: unknown; Test Date: 20211026; Test Name: Neurological examination; Result Unstructured Data: unknown
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1758604

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

kritisch

Staat: CA
Alter: 74,0
Geschlecht: M
Eingang: 04.10.2021
Impfdatum: 30.09.2021
Beginn: 02.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Asthenia Cerebrovascular accident Laboratory test Swelling

Symptomtext

Woke up and entire left side of body was swollen and dragging. Went to the ER and was admitted and diagnosed with a stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: Various Tests Ran
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: None
Allergien: Statin drugs
Vorherige Impfungen: -

VAERS 1849373

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a 21a

schwer

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 21.02.2022
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal pain Blood test Chills Computerised tomogram Diarrhoea Headache Fibrin D dimer Monoparesis Nausea Neck pain Injury Laboratory test Lung disorder Musculoskeletal pain Pain Peripheral swelling Thrombosis Ultrasound scan

Symptomtext

Felt like vomiting - nauseous, diarrhea on second day and chills, and abdominal pain. I was told that any reactions would happen within 42 days, so I kept track of the days and just thought everything was normal, so I let days go by. Then I got a pounding headaches by the 5th day and kept getting worse, stronger pain at the same time started to swell from legs and feet. Again, thought it was normal and kept pushing myself by challenging my symptoms thinking that they would go away that it was part of the good side effects of the vaccine. 2 episodes of thrombosis symptoms (leg swelling from foot to knee and pain), so I went to the ED. Then kept coming and started having neck pain, body pain, pain close to my waist and butt and realized that it was progressing and not going away. After 15 days I called PCP and I had a video appt with the doctor. She looked at my legs and feet and said that she did not see any blood clots. But said I must go to the lab to be tested. They gave me my test results but no explanation on them yet. Doctor has not made an effort to contact me to let me know what is going on with me. but they scheduled me for an ultrasound for my legs and they said that I had a blood circulation problem. They again stated seen no blood clots. However, I am still in pain. I started taking vitamin D and some other supplements in addition to NAC to help with pain and blood clots that may not be visible. I also explained to the doc that I had neck and headaches and pain in the legs and all those other issues with pain in my body were not addressed. So I called in to schedule another appointment and I was told that on Monday Morning I will be called with a confirmation video appt again to discuss test results and to also confirm cat scan appointment. I feel neglected they did all these exams and did not contact me to put me at ease after worrying about my health. I was also advised by my doctor to take long walks to help with leg pain but now also advised to use compression socks to avoid swelling and pain and take ibuprofen. Also when she did the ultrasound on my legs she said that it was discovered that I had lung damage. She asked me if I smoked, I've never smoked in my life which worried me more. Now I just hope they find a solution as every morning I find my self in pain and pushing myself to walk because my legs want to get paralyzed. I'm hoping these supplements help me to recover and that my doctor finds a solution to my injuries and that after this traumatic experience, they reconsider and exempt me from taking any more vaccine shots or I will have to take it further and use the law to take action and fight for my rights because no one wants to become disabled just by obeying to get vaccinated per president's instruction which made me hesitate and scared of loosing my job. After that I had three times requested from my doctors to be exempted from taking this because I explained to them that I had a weak system and any medication in my body reacts severely and with other experiences I would have to challenge daily my body symptoms that would affect me from going to work. I often had to call in sick and a vaccination reaction is the same thing for me. It disables my brain, it disables my body to function properly and to be able to do my daily work. Now I find myself working in pain but since I telework I could challenge it right now but if I would be returned to the building this shot would incapacitate me and I would not be able to go to work. In other words, this shot makes me disabled and unable to work. Who wants to go to work in pain and have a result of a vaccine that limits you. I find myself fighting for my life now because I don't want to be disabled, which my doctor could have prevented if she had listened to me. Considering that I as it is am a premature child, and always got sick with medications easily this could have been prevented.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: labs, CT, US of legs.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: PCN
Vorherige Impfungen: I would get very sick when I got the flu shot years ago.

VAERS 1849373

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 21.02.2022
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal pain Blood test Chills Computerised tomogram Diarrhoea Headache Fibrin D dimer Monoparesis Nausea Neck pain Injury Laboratory test Lung disorder Musculoskeletal pain Pain Peripheral swelling Thrombosis Ultrasound scan

Symptomtext

Felt like vomiting - nauseous, diarrhea on second day and chills, and abdominal pain. I was told that any reactions would happen within 42 days, so I kept track of the days and just thought everything was normal, so I let days go by. Then I got a pounding headaches by the 5th day and kept getting worse, stronger pain at the same time started to swell from legs and feet. Again, thought it was normal and kept pushing myself by challenging my symptoms thinking that they would go away that it was part of the good side effects of the vaccine. 2 episodes of thrombosis symptoms (leg swelling from foot to knee and pain), so I went to the ED. Then kept coming and started having neck pain, body pain, pain close to my waist and butt and realized that it was progressing and not going away. After 15 days I called PCP and I had a video appt with the doctor. She looked at my legs and feet and said that she did not see any blood clots. But said I must go to the lab to be tested. They gave me my test results but no explanation on them yet. Doctor has not made an effort to contact me to let me know what is going on with me. but they scheduled me for an ultrasound for my legs and they said that I had a blood circulation problem. They again stated seen no blood clots. However, I am still in pain. I started taking vitamin D and some other supplements in addition to NAC to help with pain and blood clots that may not be visible. I also explained to the doc that I had neck and headaches and pain in the legs and all those other issues with pain in my body were not addressed. So I called in to schedule another appointment and I was told that on Monday Morning I will be called with a confirmation video appt again to discuss test results and to also confirm cat scan appointment. I feel neglected they did all these exams and did not contact me to put me at ease after worrying about my health. I was also advised by my doctor to take long walks to help with leg pain but now also advised to use compression socks to avoid swelling and pain and take ibuprofen. Also when she did the ultrasound on my legs she said that it was discovered that I had lung damage. She asked me if I smoked, I've never smoked in my life which worried me more. Now I just hope they find a solution as every morning I find my self in pain and pushing myself to walk because my legs want to get paralyzed. I'm hoping these supplements help me to recover and that my doctor finds a solution to my injuries and that after this traumatic experience, they reconsider and exempt me from taking any more vaccine shots or I will have to take it further and use the law to take action and fight for my rights because no one wants to become disabled just by obeying to get vaccinated per president's instruction which made me hesitate and scared of loosing my job. After that I had three times requested from my doctors to be exempted from taking this because I explained to them that I had a weak system and any medication in my body reacts severely and with other experiences I would have to challenge daily my body symptoms that would affect me from going to work. I often had to call in sick and a vaccination reaction is the same thing for me. It disables my brain, it disables my body to function properly and to be able to do my daily work. Now I find myself working in pain but since I telework I could challenge it right now but if I would be returned to the building this shot would incapacitate me and I would not be able to go to work. In other words, this shot makes me disabled and unable to work. Who wants to go to work in pain and have a result of a vaccine that limits you. I find myself fighting for my life now because I don't want to be disabled, which my doctor could have prevented if she had listened to me. Considering that I as it is am a premature child, and always got sick with medications easily this could have been prevented.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: labs, CT, US of legs.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: PCN
Vorherige Impfungen: I would get very sick when I got the flu shot years ago.

VAERS 2128371

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CO
Alter: 24,0
Geschlecht: M
Eingang: 20.02.2022
Impfdatum: 11.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Erythema Pain Pain in extremity Superficial vein thrombosis Ultrasound scan abnormal

Symptomtext

The patient is a 24 y.o. male who presents for evaluation of left arm pain. Patient was here yesterday seen for alcohol withdrawal symptoms and intoxication and had an IV line placed at the AC joint and states that he started noticing increased pain and some redness around the IV insertion site. Denies any weakness or numbness to the extremity. Patient was concerned of possible blood clot and so came to the ED for evaluation. There are no other modifying factors or associated symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Superficial vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound with evidence of superficial venous thrombosis with 0.8 cm proximity to the deep venous system.
Aktuelle Erkrankungen: Alcohol intoxication with symptoms of withdrawal at ED visit 10/11/2021
Vorgeschichte: Alchoholism, anxiety
Andere Medikamente: "cloNIDine HCL (CATAPRES) 0.1 mg tablet hydrOXYzine pamoate (VISTARIL) 50 mg capsule traZODone (DESYREL) 50 mg tablet "
Allergien: None
Vorherige Impfungen: -

VAERS 2058446

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

schwer

Staat: TN
Alter: 38,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 27.10.2021
Beginn: 09.12.2021
Tage bis Beginn: 43,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Antiacetylcholine receptor antibody Blood test Facial paralysis Myasthenia gravis Paraesthesia oral

Symptomtext

4 days post shot, got tingling in upper lip? Exactly 6 weeks later on December 9 21 I developed a droopy right eye? That was later deemed to be myasthenia gravis through a blood test , after visiting an optometrist, ophthalmologist, and neuro ophthalmologist

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Lab test AchR Abs 1/11/22 from lab 4.76 result (positive is more than 0.4)
Aktuelle Erkrankungen: None
Vorgeschichte: Raynauds
Andere Medikamente: Escitalopram 10mg
Allergien: None
Vorherige Impfungen: -

VAERS 2021540

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: TX
Alter: 38,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 30.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal pain upper Blood test Chest discomfort Chest pain Cold sweat Diarrhoea Dyspnoea Echocardiogram Electrocardiogram Fatigue Head discomfort Headache Loss of consciousness Muscular weakness Nausea Pain in extremity Pyrexia Somnolence

Symptomtext

CHEST PAIN, TIGHTNESS OF CHEST, INCREASE PRESSURE IN HEAD, HEADACHES, STOMACH PAIN WHEN EATING MEAT, DIARRHEA, SHORT BREATHING, FEVERS, COLD SWEAT, PAIN IN ARMS, FATIGUE, WEAKNESS OF LIMBS, UNABLE TO TAKE DEEP BREATHS, DIMINISHED AND UNFOCUSED VISION, BLACKOUTS, SUDDEN ONSETS OF SLEEPINESS, VERTICO, NAUSEA. SYMPTOMS BEGAN ON THE DAY OF THE INJECTION. 30 SEP 2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: ER VISITS CONDUCTED EKG, MULTIPLE BLOOD TESTS CONDUCTED, XRAYS, ECHO, ULTRASOUND IMAGING.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: ANTHRAX 2004

VAERS 1998659

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: MN
Alter: 47,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 01.10.2021
Beginn: 01.01.2022
Tage bis Beginn: 92,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Intensive care Tracheostomy Vaccine breakthrough infection

Symptomtext

Fully vaccinated with J&J, not boosted. COVID infection breakthrough and admit to inpatient ICU. Chronic trach.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1935358

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 211A21A

schwer

Staat: MN
Alter: 41,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 22.09.2021
Beginn: 09.10.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Bell's palsy Magnetic resonance imaging Neuralgia

Symptomtext

Bells Palsy! Nerve Pain in my hands, left leg and toes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: multiple doc visits MRI12/14/2021
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: none
Vorherige Impfungen: -

VAERS 1959081

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: OR
Alter: 82,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 29.11.2021
Beginn: 07.12.2021
Tage bis Beginn: 8,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Angiogram Angiogram cerebral Mydriasis Ophthalmological examination abnormal Platelet count normal Retinal vein thrombosis Vision blurred Visual impairment

Symptomtext

Odd vision in Right eye started 5 days after J & J booster. 2 days later vision became blurry. Went to ophthalmology who urgently referred patient to retina specialist. Specialist found blood clot in retinal vein of Right eye. No increased eye pressure. Platelet count normal. Follow up on Jan 5 for pressure check with retina specialist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Retinal vein thrombosis
Hospital-Tage: -
Labordaten: Dilated eye exam. Retinal exam. Angiography of brain/eye
Aktuelle Erkrankungen: Headache
Vorgeschichte: A-fib, chronic HTN hypercholesterolemia PBH low B12 low Vit D
Andere Medikamente: Eliquis 5 mg bid Vit C 500 q day atorvastatin 40 mg q day B-complex vitamin daily Calcium glutinate 1000 mg daily Vit D 1000 iu daily finasteride 1 mg daily folic acid 1 mg daily metoprolol tartrate 50 mg q AM and 75 mg q PM MVI daily topam
Allergien: NKDA No food allergies No environmental allergies
Vorherige Impfungen: Patient developed a chronic headache after his 2nd Pfizer vaccine.

VAERS 1942689

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CO
Alter: 21,0
Geschlecht: M
Eingang: 12.12.2021
Impfdatum: 12.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Head injury Loss of consciousness Vomiting

Symptomtext

PATIENT WAS GIVEN VACCINATION. HE GOT UP A FEW MINUTES LATER AND PASSED OUT. HE LOST CONSCIOUSNESS FOR APPROXIMATELY 3-5 SECONDS AND HIT HIS HEAD . AFTER APPROXIMATELY 5 MINUTES PATIENT VOMITTED. SHORTLY AFTER HE WAS ALERT AND AWARE OF SURROUNDINGS. PATIENT FELT COMFORTABLE EXITING THE BUS AND WALKING TO HIS CAR ALONG WITH MEDICAL STAFF. MEDICAL STAFF ENCOURAGED ADDITIONAL MEDICAL ASSISTANCE FOR HEAD; PATIENT AND MOM DECLINED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: NO
Vorgeschichte: NO
Andere Medikamente: N/A
Allergien: NO
Vorherige Impfungen: -

VAERS 1921671

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: WA
Alter: 43,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Nausea Syncope

Symptomtext

Patient had an episode of Syncope for 30-45 seconds 2-3 minutes after receiving their vaccine. Patient felt nasuseous and sat down, no falls occurred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: N/A.
Vorgeschichte: N/A.
Andere Medikamente: N/A.
Allergien: No allergies attested in the initial screening questions.
Vorherige Impfungen: Patient stated they often faint post any injection.

VAERS 1905982

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: -
Alter: 34,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Nausea Presyncope

Symptomtext

near-syncope and nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: unknown
Andere Medikamente: oral contraceptive, escitalopram
Allergien: none
Vorherige Impfungen: -

VAERS 1873440

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: WI
Alter: 46,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 20.10.2021
Beginn: 10.11.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Deep vein thrombosis Pain Superficial vein thrombosis Ultrasound Doppler abnormal Venous occlusion

Symptomtext

Patient become symptomatic on 11-10-2021 of a DVT in distal left lower extremity. confirmed by Ultrasound on 11-15-21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound on 11-15-21 confirmed Peroneal veins are occluded in the proximal calf with one of the paired veins occluded to the mid calf and Thrombosed superficial gastrocnemius vein in the region of patient's pain.
Aktuelle Erkrankungen: None
Vorgeschichte: GE reflux subclinical hypothyroidism
Andere Medikamente: Marlissa (oral contraceptive) Biotics optimal EFA Biotics research NAC Integrative therapeutics panplex 2
Allergien: amoxicillin (nausea) ASA (hallucinations) Hydrocodone (nausea/vomiting)
Vorherige Impfungen: -

VAERS 1854381

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: AR
Alter: 18,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Pain in extremity Syncope

Symptomtext

Approximately five minutes post-vaccine administration (while patient was sitting in a chair in a monitored waiting area), she grabbed her right arm, stated "that does hurt," and briefly fainted. Public health RN and APRN responded within seconds. Patient alert and oriented to person, place, time and situation. Checked patient vitals signs at 16:05 (BP 108/41) and 16:10 (BP 95/65); all others within normal limits. Provided patient with bottle water, ice pack and cool wet cloth on forehead. After patient waited for an additional 15 minutes, she requested to be allowed to leave the facility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1785636

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: TX
Alter: 28,0
Geschlecht: M
Eingang: 03.11.2021
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: ja Erholt: nein

Blood potassium decreased Computerised tomogram normal Concussion Fall Head injury Dizziness Dyskinesia Face injury Memory impairment Muscle tightness Musculoskeletal stiffness Seizure Unresponsive to stimuli

Symptomtext

Within 10 minutes of receiving the shot, I had a seizure. I have never had a seizure before in my life. The seizure caused me to fall off of the bed in the room and hit my head on the floor. With the help of EMT, I regained awareness 20-30 minutes after the seizure began. The fall cause me to split my head open near my eyebrow. I was taken to the emergency room and received several stitches at the wound site. The emergency room doctor also told me I had a minor concussion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: CAT scan - normal - 10/12/21 Finger blood prick - potassium slightly low - 10/12/21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Over-the-counter multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1826033

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: WA
Alter: 74,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 25.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Epistaxis Full blood count Metabolic function test Thrombosis

Symptomtext

Patient was given the vaccine 10/25 and walked into clinic this am , urgently holding her nose asking to be seen by a provider. Pt was triaged by RN first , then placed on the provider schedule as a same day urgent/walk-in appointment. X3 episodes of epistaxis w/ clots lasting >30 min each in last two days. In clinic Pt is 3 days s/p receiving her first dose of Johnson and Johnson covid-19 vaccine. She endorses PMH of at least X1 episode of epistaxsis per year, not w/ clots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Check CBC w/ auto diff Check PT/PTT, plasma Check CMP, serum or plasma Received PT/INR all
Aktuelle Erkrankungen: none
Vorgeschichte: Patient endorses PMH of at least X1 episode of epistaxsis per year, not w/ clots.
Andere Medikamente: none
Allergien: Allergy to sulfa antibiotics
Vorherige Impfungen: -

VAERS 1825503

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: WA
Alter: 48,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cold sweat Dizziness Hyperhidrosis Loss of consciousness Malaise

Symptomtext

48 yo male received JJ Covid 19 vaccine Lot #211A21A, 1st dose at 1625. At 1628, while in the observation area, he stated "not feeling well and going to pass out." ET, RN, stood in front of pt. , held his shoulders, called for assist, place pulse ox on index finger, HR 44, O2 sat 97%,, pt passed out momentarily, skin cool/clammy to touch, diaphoretic. At 1630 Pt transferred to WC and taken to room and transferred to guerney to lie down, with stand by assist. Pt. stated "feeling better.' Pt. stated "I usually pass out when getting shots" before receiving vaccine, stand by RN at pt side during vaccine, pt then walked to observation area with c/o dizziness. Pt. reported he was "reluctant about taking the vaccine, but needed it for work..Pt. denies CP, SOB, NV, has no hx of diabetes, and said he did not eat or drink much today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: 1628 BP na HR 44 RR na O2SAT 98% Sitting 1630 BP 116/84 HR 72 RR 16 O2Sats 97% Supine 1640 BP 118/88 HR 71 RR 16 O2 Sat 97% Supine 1652 BP 128/80 HR 71 RR 16 O2 Sat 97% Sitting 1658 BP 115/78 HR 69 RR 16 )3 Sats 96 Standing Pt discharged from our care at 1700, ambulated by self to car. VS stable. Impression: Vasal vagal response. Recovered and sent home.
Aktuelle Erkrankungen: none
Vorgeschichte: Pt reports hx of fainting when getting shots
Andere Medikamente: none
Allergien: NKA
Vorherige Impfungen: -

VAERS 1808596

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211 a21a

schwer

Staat: HI
Alter: 31,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 13.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Computerised tomogram head Confusional state Dizziness Dysarthria Electrocardiogram Fatigue Feeling abnormal Feeling hot Full blood count Hyperhidrosis Malaise Metabolic function test Mobility decreased Pain in extremity Paraesthesia Piloerection Syncope

Symptomtext

On 10/15 Symptoms began with tingling in the hands and feet. Patient began to get hot and light headed. Throughout the following days he experienced exhaustion, brain fog, tingling over his entire body, excessive sweating, faint-like spells, dizziness and confusion. On 10/19 he was complaining of feeling unwell and tingling through his body, pain in his legs and feet. Tingling though his neck area. He had a sensation of always ?feeling? his arms in a way he?s never experienced before. Around 8:15pm Patient was laying on his back and his entire body was covered in goose bumps, he was unable to move like some kind of paralysis, his body was locked in place. His muscles were all engaged. he was able to slur 911. A few minutes later he came to and was fully conscious. By 8:30 he was admitted to the ER. Now on 10/22 his symptoms of tingling and exhaustion are ever present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: CT BRAIN WO CONTRAST ECG 12 led - cv CBC w differential Differential automated Serum indices Basic metabolic panel bmp Troop in 85025 cbc auto w auto
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1801987

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 28.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Blood test normal Cognitive disorder Disability Impaired work ability Loss of control of legs Loss of personal independence in daily activities Magnetic resonance imaging head normal Musculoskeletal disorder Seizure Speech disorder Tremor Vaccination complication

Symptomtext

Uncontrollable, full body convulsions, almost daily. When not fully convulsing, constant tremors are present. Does not have full control of hands and legs, struggles with normal daily functions. Speech ability and cognitive capabilities have been challenged as well. Doctors have no idea what is happening, but all believe it is a reaction to the vaccine. Doctors have no idea what to do other than prescribe muscle relaxers, which do nothing. We have found that over the counter Benadryl helps to a degree. Josiah has been referred to a Neurologist, the neurologist also has no idea. Pt has lost his job and is facing having to quit school due to disability.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Routine blood work each time he gets sent to the ER by ambulance, tests always come up normal. Brain MRI done on Tuesday 10/12/2021. Nothing abnormal found. Waiting for EEG appointment on November 5.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Cheese
Vorherige Impfungen: -

VAERS 1801761

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 22.09.2021
Beginn: 16.10.2021
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Asthenia Blood test Chest pain Computerised tomogram Dizziness Dysstasia Gait disturbance Head discomfort Hypotension Migraine Palpitations Seizure Syncope Ultrasound scan X-ray

Symptomtext

Syncope episode with seizure. Constant migraine. Low blood pressure. Chest pains, Heart palpitations, Pulsating to the brain. Weakness. Unable walk or stand for short periods. Dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: CT Scan Blood test Ultrasound Xrays Cardiologist Referral
Aktuelle Erkrankungen: Lupus, Fibromyalgia, Thalessemia Anemia trait
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1796528

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 27.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Bell's palsy Urticaria

Symptomtext

Hives on B LE occurred on 10/01/2021; L sides Bell?s Palsy developed on 10/14/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: ED visit on 10/15/2021
Aktuelle Erkrankungen: Covid+ 09/05/2021; Covid recovered 9/20/2021
Vorgeschichte: None
Andere Medikamente: Krill oil, vitamin C , D3, probiotics, progesterone, estradiol patch, COQ10
Allergien: None
Vorherige Impfungen: Flu vaccine

VAERS 1789933

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anaphylactic reaction Chest X-ray Computerised tomogram neck Dysphagia Dysphonia Dyspnoea Intensive care Laboratory test Rash Swallow study Swelling

Symptomtext

Anaphylactic reaction, started approx 25mins after administration. Rash, swelling, airway concerns. Emergency telephoned by facility; transfer to ED. Multiple epinephrine injections, steroids, Benadryl, breathing treatments, approx 6 days in ICU and further hospitalization. Continued issues with shortness of breath, voice and swallowing problems.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: 9,0
Labordaten: Chest xray, labs, swallow evals, ct neck scan
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, DM2, SVT
Andere Medikamente: Prilosec, losartan, spironolactone, bumex, gabapentin
Allergien: Sesame; pcn; contrast dye; chloraprep
Vorherige Impfungen: -

VAERS 1780131

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: TX
Alter: 31,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Dizziness Syncope

Symptomtext

Patient was sitting in the waiting area after his vaccination for the standard 10-15 minute observance period, when he became light-headed and fainted while seated in a standard height chair. 911 was immediately called and the patient was aroused after about 10-15 seconds. He remained in the recovery position until EMS arrived and escorted him outside of the building to their ambulance to check his vitals and check on him. He did report to me before EMS arrived that he has fainted several times in the past after giving blood. On his vaccine administration consent form, he did select "no" when asked if he had ever had a serious reaction after receiving a vaccination in the past.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1776858

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

schwer

Staat: CO
Alter: 23,0
Geschlecht: F
Eingang: 11.10.2021
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Presyncope Supine position

Symptomtext

Patient became presyncopal shortly after vaccination. She was placed in supine position, with legs elevated. Vitals WNL, symptoms completely resolved with position changes. No other symptoms reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hx of asthma and anemia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1776566

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

schwer

Staat: MO
Alter: 62,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Hyperhidrosis Pallor Psychogenic seizure Trendelenburg position

Symptomtext

Pale, diaphoretic, dizziness, pseudo seizure. Pt placed in reverse Trendelenburg on the floor with feet in a chair, vital signs taken and patient was given time to recover.Patient left building on own accord without issue. Pt informed to watch for further issues and contact 911 if needed; pt stated understanding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Psychogenic seizure
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Unk
Andere Medikamente: Unk
Allergien: Unk
Vorherige Impfungen: -

VAERS 1772100

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cold sweat Hyperhidrosis Seizure

Symptomtext

Post injection, pt was observed to have "slight convulsing", clammy, sweaty hands. HR and SpO2 WNL., BP normal. Denied dizzyness, chest pain, nausea. at 10:10 pt noted to show improvement in skin conditions. Pt ate granola bar, drank juice and water, tolerated well. She ambulated without difficulty, steady gait. At 10:40 pt left clinic, denied SOB, pain, dizziness. She was accompanied by her mother.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1762126

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CA
Alter: 30,0
Geschlecht: M
Eingang: 05.10.2021
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cyanosis Dizziness Hyperhidrosis Syncope

Symptomtext

dizziness ,fainting cyanosis bluish discoloration. sweating . we injected Epipen . Patient recovered in 5 minutes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1759789

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: TN
Alter: 21,0
Geschlecht: M
Eingang: 04.10.2021
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fall Syncope

Symptomtext

After his vaccine, the patient was sitting in a chair, fainted and collapsed onto the floor. Ambulance was called, which the patient refused.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1758990

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: NV
Alter: 25,0
Geschlecht: M
Eingang: 04.10.2021
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cold sweat Nausea Pallor Syncope

Symptomtext

Fainted, pale, skin felt cold and clammy, patient reported nausea, BP was 107/73, pulseox: 98%, Pulse: 65 bpm. Patient given a lollipop, cookies, and water as well as an ice pack. Patient sat and rested for approximately 20 minutes after event after which he reported feeling much better and left.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1757077

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: WA
Alter: 41,0
Geschlecht: F
Eingang: 03.10.2021
Impfdatum: 25.09.2021
Beginn: 25.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain Axillary pain Chills Headache Myalgia Nausea Pain Photopsia Tenderness Thrombosis Vaginal haemorrhage

Symptomtext

Severe chills, muscle aches, shooting pains in calves, hamstrings and back, rash on neck and side, spotting and blood clots coming from vagina when not time for regular mensural cycle, abdominal cramping, severe headache, flashing light when closing eyes, tenderness and pain under armpits, nausea all lasting over a week after vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Sumatriptan
Allergien: N/A
Vorherige Impfungen: -

VAERS 1757002

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 02.10.2021
Impfdatum: 28.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Facial paralysis Muscular weakness Pyrexia

Symptomtext

- High Fever - Slight Paralysis on right side of face - Weakened leg muscles

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Migraines / endometriosis
Vorgeschichte: Neuropathy / GBS diagnosed in 2013 (residual symptoms since then)
Andere Medikamente: Vitamin C, Valerian Root at night, SAMe and Vitamin D
Allergien: Yes.
Vorherige Impfungen: Flu vaccine / 23

VAERS 1754514

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

schwer

Staat: CA
Alter: -
Geschlecht: U
Eingang: 01.10.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Acute cardiac event Anaphylactic reaction Arthralgia Back pain Blood test Dyspnoea Electrocardiogram abnormal Flank pain Headache Hypoaesthesia Pain in extremity Paraesthesia Pharyngeal swelling Urticaria X-ray

Symptomtext

11:43 shortness of breath, pain on left, side tingling, throat swelling, 12:14 hives, numbness in face -returned to urgent care with severe headach, anaphylactic symptoms, extreme flashing pain in upper back, left arm and shoulders-ekg indicated a cardiac event and was sent to Hospital. Tested and treated, released at 11pm. Next morning (10/1/2021) 08:30 anaphylaxis, went to Hospital -treated and released at 3pm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: 9/30 ekg, blood draw at urgent care 9/30 ekg, blood draw, x-ray meds (records available) at Hospital 10/1 IM and IV fir anaphylaxis at Hospital (records available)
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Flu shot around 2006

VAERS 1750168

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: TX
Alter: 20,0
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

Hyperhidrosis Loss of consciousness Pallor Seizure Vomiting

Symptomtext

Patient left pharmacy under there own power, and interacted with staff fine. Uncle of patient stated in the car ride home, approx. 15min after vaccination, the patient threw up, convulsed, and loss conciseness. Our Pharmacist meet patient in the parking lot, approx. 20min after vaccination, patient was visibly sweeting and had a loss of color to face.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Recommended to visit Urgent Care or Hospital to evaluate further
Aktuelle Erkrankungen: none given/listed
Vorgeschichte: none given/listed
Andere Medikamente: none given/listed
Allergien: none given/listed
Vorherige Impfungen: -

VAERS 1745113

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CA
Alter: 24,0
Geschlecht: M
Eingang: 29.09.2021
Impfdatum: 28.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Hyperhidrosis Loss of consciousness Pallor Syncope

Symptomtext

Client had a syncopal episode after a few mins of vaccine administration. Client loss consciousness for a few seconds and quickly came back. He was sweating and was pale. Water was given water and after a few minutes his color was back and was answering all questions with no problem. EMS were called on site, client declined to be transferred to hospital. He was stable and walked with a steady gait to catch his ride.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none reported
Vorgeschichte: none reported
Andere Medikamente: None reported
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1737326

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

schwer

Staat: OH
Alter: 30,0
Geschlecht: F
Eingang: 27.09.2021
Impfdatum: 27.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Syncope

Symptomtext

Patient fainted about 5 to 7 minutes after the injection. We had to use the ammonium inhalant.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: -
Allergien: none
Vorherige Impfungen: fainting

VAERS 1737170

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 27.09.2021
Impfdatum: 27.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Heart rate increased Hypotonia Lethargy Pulse abnormal Seizure Tremor Unresponsive to stimuli

Symptomtext

Patient arrived to COVID vaccine clinic around 9 am on 9/27. She was very nervous to get her shot and verbalized this to other patients while waiting in line. About 15 minutes into her 30-minute observation (allergic to Penicillin and bee venom) a staff member was grabbing an emesis bag for the patient, so I went to assess her. As I approached, the patient slumped over onto the desk and became unresponsive. Patient began shaking all over. I lowered her to the ground and held her head for the duration of the seizure for safety. Another patient came over stating she is a nurse and checked the patient?s pulse, stating it was very fast and weak. Patient was unresponsive and shaking for 1-2 minutes. When the shaking ended, she opened her eyes and was able to ask where she was. After another minute or so, we assisted patient onto the gurney and patient was able to help by using her legs to push up from the floor. We took patient to the ED for evaluation. Patient remained lethargic but was responsive to voice while en route to the ED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Penicillin Bee venom
Vorherige Impfungen: -

VAERS 1735626

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: TX
Alter: 44,0
Geschlecht: M
Eingang: 26.09.2021
Impfdatum: 23.09.2021
Beginn: 24.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Adverse event Blood test Computerised tomogram Incoherent Migraine Scan with contrast Seizure

Symptomtext

Adverse events: severe migraine, convulsion, incoherent speech Treatment: Ambulance, paramedics, had to stabilize in order to be taken to ER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 1,0
Labordaten: CAT scan (including one with contrast), full blood work
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1728791

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: CO
Alter: 26,0
Geschlecht: M
Eingang: 23.09.2021
Impfdatum: 23.09.2021
Beginn: 23.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Dizziness Presyncope

Symptomtext

Patient felt faint after the vaccine, had pre-syncopal episode. Laid on cot and made full recovery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: unknown

VAERS 1723810

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

schwer

Staat: WA
Alter: 45,0
Geschlecht: M
Eingang: 22.09.2021
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Loss of consciousness Nausea

Symptomtext

PATIENT FELT VERY NAUSEATED, AND PASSED OUT FOR 20 TO 30 SECONDS BEFORE BEING CONSCIOUS. HE SAID AS A CHILD HE WAS CHASED AROUND WITH NEEDLES AND HE IS VERY AFRAID OF NEEDLES. AFTER FEW MINUTES HE WAS COMPLETELY FINE AND HE WALKED OUT OF THE PHARMACY ON HIS OWN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BLOOD PRESSURE WAS 130/82 WHEN THE MEDICS CHECKED IT.
Aktuelle Erkrankungen: SEVERE ANXIETY TO NEEDLES
Vorgeschichte: ANXIETY
Andere Medikamente: CLONAZEPAM
Allergien: PENICILLIN, DILAUDID
Vorherige Impfungen: -

VAERS 2321948

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 16.06.2022
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Angina pectoris Blood test Cardiac monitoring Dizziness Dyspnoea Hypoaesthesia Immediate post-injection reaction Pain Pain in extremity Palpitations

Symptomtext

Immediate heart pain, nausea, difficulty breathing, pain in arm radiating down to fingers, numb fingers and hand pain. Staff came and put monitor on me in less than a minute due to heart racing and dizzy. Stayed at facility over injectors watch named "private". Facility called me for next few days to see how I was progressing. I was having all the above issues and made appointments with my doctor. I continued to have leg pain on left side, numb fingers and radiating arm pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Doctor did exam, ran blood work, and next week I am seeing a new doctor to see why i am still having these issues.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Lipitor and Felodipine
Allergien: bee stings and reaction to penicillin
Vorherige Impfungen: Shingles vaccine- pain and swelling at arm

VAERS 2234237

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 14.04.2022
Impfdatum: 26.09.2021
Beginn: 26.09.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Dyspnoea Dyspnoea exertional Headache Influenza like illness Insomnia Pain Pyrexia Sinus congestion

Symptomtext

Experienced strong flu-like symptoms (fever, body aches) for several days beginning a few hours after injection. Experiencing chest pains and shortness of breath especially upon exertion. Experiencing insomnia. Experiencing increased sinus congestion and headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Montelukast, Loratadine
Allergien: Compazine
Vorherige Impfungen: -

VAERS 2226585

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: KY
Alter: 52,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood pressure fluctuation Chest X-ray normal Chest discomfort Echocardiogram Electrocardiogram Q wave abnormal Laboratory test normal Myocardial necrosis marker normal Palpitations Paraesthesia

Symptomtext

in late Feb/early March 2022 started experiencing some intermittent palpitations, chest discomfort/squeezing sensation; one episode of tingling in chest and blood pressure fluctuations; seen in ER early March 2022 for chest pressure and had cardiac workup done; sent to cardiologist for abnormal EKG showing Qwave; ECHO completed; stress test scheduled and pending; no prior cardiac history or family history; concern that vaccine could possibly be related to the events/symptoms; unknown etiology.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: cardiac enzymes were normal in ER; EKG showed Qwave abnormalties; labs otherwise unremarkable, CXR normal; have upcoming stress testing scheduled
Aktuelle Erkrankungen: Hypothyroidism, Hyperaldosteronism, Osteopenia, Mitral Valve Regurgitation-mild, Dry Eye Syndrome, Psoriasis, Vit D deficiency
Vorgeschichte: Hypothyroidism, Hyperaldosteronism, Psoriasis, Mild Mitral Valve regurgitation
Andere Medikamente: Synthroid, Spironolactone, Vitamin D3, TheraTears, Calcium w/ Vitamin D, Magnesium, Topical Betamethasone, Topical Alovate/Nystatin compounded cream, Xiidra eye drops
Allergien: NKDA; no food allergies
Vorherige Impfungen: -

VAERS 2149538

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 01.03.2022
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

Body temperature increased Dyspnoea Fatigue Headache Laboratory test Pain X-ray

Symptomtext

High Temperature for up to 4 days ,severe fatigue and body aches as well as getting out of breath and headaches which have continued since the the day of the vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Lab work and X-rays performed November 19th 2021
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: no
Allergien: No
Vorherige Impfungen: -

VAERS 2148195

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 01.09.2021
Beginn: 01.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Heart rate increased Immediate post-injection reaction Magnetic resonance imaging Tachycardia Tinnitus

Symptomtext

Immediate pulse / swoosh in right ear, severe tinnitus , and tachycardia episodes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: ENT Dec 2021. MRI Feb 2021. ER visits January 9 2022. ER visit Feb 2022.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: sulfa
Vorherige Impfungen: -

VAERS 2146572

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: 57,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Magnetic resonance imaging head Paraesthesia

Symptomtext

Constant tingling of both arms and hands occurred the day after I received the Covid-19 Janssen Vaccine. Cerebral hemispheres which (per read) most likely represents vasospastic phenomena of migraines vs. small vessel ischemic changes in a patient with appropriate CV risk factors. As well there is partially empty sella, which is a benign finding, but is occationally reported to be associated with headaches. Given no structural abnormalities to explain patient's symptoms, temporal relation to his vaccination, and newer reports associated with the J and J vaccine (though patient does not have, but isolated sensory dysfunction) there is possibility that patient's symptoms are a vaccine side effect. Discussed the importance of documenting his symptoms in VAERS so that further investigation can be done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: MRI of brain done on Feb 2, 2022, and MRI of neck done on Feb 15, 2022. MRI demonstrates multiple small foci of increased abnormal T2 prolongation in subcortical white matter of B/L
Aktuelle Erkrankungen: none
Vorgeschichte: Coronary Artery Disease; High Blood Pressure
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2134364

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 14.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 pneumonia

Symptomtext

Pneumonia due to COVID-19 virus, received dexamethasone and remdesivir during hospital stay. Discharged home. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 14,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2119372

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

moderat

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Burning sensation Dyspepsia Fall Hypoaesthesia Muscle spasms Myalgia Nervous system disorder Paraesthesia

Symptomtext

Immediate numbness and tingling down right arm. Sustained numbness and tingling in right hand for 4 months. Immediate neurological and muscular burning in legs. Muscle seizure in things causing me to fall down multiple times (occurred 5 times over 3 month period). Immediate heartburn from time of injection to present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2084824

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: -
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: -
Beginn: 23.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Arthralgia Blood pressure measurement Bone pain Electrocardiogram Fatigue Feeling abnormal Feeling hot Headache Hypersomnia Hypertension Influenza like illness Lymphadenopathy Myalgia Neck pain Pain in extremity Pain of skin Scan Swelling

Symptomtext

NUMBING PAIN IN NECK; WEIGHT GAINING; NUMBING PAIN IN ARM; RIGHT SIDE OF NECK A BIT SWOLLEN; SWELLING IN CHEST; SWOLLEN MUMP WHERE THE NECK SHOULDER AND COLLAR BONE MEET; HEADACHE; SWOLLEN LYMPH NODES ON BEGINING OF THE NECK AND CLOSE TO COLLAR BONE; FLU LIKE SYMPTOMS; SENSITIVE TO COLD; PAINFUL SKIN; PAIN IN ANKLES; SORE SHOULDER; JOINTS IN KNEES WERE PAINFUL SPECIALLY THE LEFT ONE (NUMB/PAIN); HIGH BLOOD PRESSURE; FELT HOT; BONE ACHES AROUND THE JOINTS (NUMB/PAINFUL); WEIRD FEELING; SLEPT MORE; MUSCLES ACHES; FATIGUED; This spontaneous report received from a patient concerned a 34 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, administered on 22-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 23-DEC-2021, the patient experienced bone aches around the joints (numb/painful), weird feeling, slept more, muscles aches, and fatigued. On 24-DEC-2021, the patient experienced high blood pressure. On 24-DEC-2021, the patient experienced felt hot. On 24-DEC-2021, the patient experienced joints in knees were painful specially the left one (numb/pain). On 25-DEC-2021, the patient experienced swollen lymph nodes on begining of the neck and close to collar bone, sensitive to cold, painful skin, flu like symptoms, pain in ankles, and sore shoulder. On JAN-2022, Laboratory data included: Blood pressure (NR: not provided) increased, 164/113, and Scan (NR: not provided) no clot found. On 13-JAN-2022, the patient experienced right side of neck a bit swollen, swelling in chest, swollen mump where the neck shoulder and collar bone meet, and headache. Laboratory data included: EKG (NR: not provided) all normal. On an unspecified date, the patient experienced numbing pain in neck, weight gaining, and numbing pain in arm. Treatment medications (dates unspecified) included: ibuprofen, paracetamol, and ascorbic acid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from bone aches around the joints (numb/painful) on 01-JAN-2022, weird feeling, flu like symptoms, and muscles aches on 30-DEC-2021, felt hot, sensitive to cold, painful skin, joints in knees were painful specially the left one (numb/pain), and pain in ankles, and fatigued on 26-DEC-2021, had not recovered from high blood pressure, sore shoulder, swollen lymph nodes on begining of the neck and close to collar bone, right side of neck a bit swollen, numbing pain in arm, headache, swollen mump where the neck shoulder and collar bone meet, and numbing pain in neck, and the outcome of swelling in chest, weight gaining and slept more was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 202201; Test Name: Blood pressure; Result Unstructured Data: increased; Comments: (17X/1XX); Test Date: 202201; Test Name: Scan; Result Unstructured Data: no clot found; Test Date: 202201; Test Name: Blood pressure; Result Unstructured Data: 164/113; Test Date: 20220113; Test Name: EKG; Result Unstructured Data: all normal
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2084738

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: FL
Alter: -
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: -
Beginn: 18.01.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Diarrhoea Headache Pyrexia SARS-CoV-2 test Vomiting

Symptomtext

DIARRHEA; FEVER; CHEST PAIN; HEADACHE; VOMITING; This spontaneous report received from a patient concerned a male of unspecified age. The patient's height, and weight were not reported. The patient's concurrent conditions included: sometimes general headaches, and other pre-existing medical conditions included: Patient had no known allergies. The patient received Covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, administered on 24-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On 18-JAN-2022, the patient experienced chest pain, headache, and vomiting. Laboratory data included: COVID-19 virus test (NR: not provided) Negative. On 19-JAN-2022, the patient experienced diarrhea, and fever. The action taken with Covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from headache, chest pain, diarrhea, and fever, and the outcome of vomiting was not reported. This report was non-serious. The suspected product quality complaint has been confirmed to be voided (did not meet PQC criteria as the reporter indicates they were exposed to someone with Covid and they later felt ill but tested negative for Covid. There is no product quality issue described in the information reported. Approval to void this record due to no PQC identified) based on the PQC evaluation/investigation performed. Sender's Comments: V0: Medical assessment comment not required as per standard procedure as the case is assessed as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20220118; Test Name: COVID-19 virus test; Result Unstructured Data: Negative.
Aktuelle Erkrankungen: Headache (Different from this headache which is stabbing pain behind ears.)
Vorgeschichte: Comments: Patient had no known allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2059341

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 24.09.2021
Beginn: 23.01.2022
Tage bis Beginn: 121,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Antinuclear antibody positive Arthralgia Blood test abnormal C-reactive protein increased Disturbance in attention Fatigue Gait disturbance Haemoglobin decreased Injected limb mobility decreased Loss of personal independence in daily activities Movement disorder Neck pain Pain Periarthritis Platelet count increased Red blood cell sedimentation rate increased Red cell distribution width increased Rheumatoid arthritis

Symptomtext

I had extreme pain in my right knee and ankles. I then started not being able to move my right shoulder. I was having trouble concentrating and extremely tired 48 hours after the shot. I waited 45 days after the shot to seek medical attention due to the information received about the vaccine from the lab. By the time I went to a doc in the box, I was barely able to move. I had to have assistance opening up the car door and walking into the doctor's office. The first doctor gave me Tramadol 100 MLG tables and told me to go see an Orthopedic doctor. I set an appointment to see an orthopedic doctor who diagnosed me with a frozen shoulder but could not explain the pain in my knee ankles neck and upper body. He asked me to do some blood work to check on some things. After receiving my results he informed me to see an RA doctor. I saw Dr., she started me on Methotrexate 2.5 MG and ordered blood work. She then diagnosed me with RA. However, the Methotrexate is not working. More blood work was taken.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: 11/11/2021 -10:03 - ANA Screen, IFA - Positive Ana Titer - 1:160H Ana Pattern- Nuclear, Dense Fine Speckled C-Reactive Protein - 76.2 12/06/2021 -10:54 AM ANA Screen, IFA - Positive ANA Titer - 1:160H ANA Pattern - Nuclear, Dense Fine Speckled Rheumatoid Factor - 55 H Platelet Count - 431 H C- Reactive Protein - 35.9 Collection : 01/15/2022 9:30 SE Rate Modified Westergren - 60H Hemoglobin - 11.6 L RDW - 15.6 H Platelet Count - 466 H C- Reactive Protein - 37.3
Aktuelle Erkrankungen: None
Vorgeschichte: Type 1 Diabetic, High Blood Pressure, Fibromialga
Andere Medikamente: Insulin, Trulicity, Metformin, Losartan
Allergien: Alegra
Vorherige Impfungen: -

VAERS 2052258

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: 25,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Blood glucose increased Cough Decreased appetite Depression Dyspnoea Insomnia Lethargy Migraine Muscle spasms Nausea Oropharyngeal pain Parosmia

Symptomtext

Joint pain (shoulders, elbows, wrists, fingers, hips, knees, ankles, toes), Muscle Spasms, Migraine, Nausea, Loss of Appetite, SOB, Lethargy, Insomnia, Parasomnia, Elevated BG (compared to normal trends), Depression, Sore Throat, Cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood glucose since vaccine: 1/19/22 04:04 PM - 265mg/dL 1/19/22 06:40 PM - 327mg/dL 1/19/22 07:36 PM - 293mg/dL 1/20/22 03:59 AM - 287mg/dL 1/20/22 09:54 AM - 276mg/dL
Aktuelle Erkrankungen: COVID-19 positive 12/21/2021
Vorgeschichte: Type 1 diabetes
Andere Medikamente: Novolog, Toujeo, Adderall
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2051547

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: KS
Alter: 70,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 26.10.2021
Beginn: 15.11.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Fibromyalgia Pain in extremity

Symptomtext

Shortly after getting my second (booster) shot I experienced a flare-up of fibromyalgia in my right arm that I did not experience with the first shot. This is the same arm I got my shots in. The pain has continued for more than 2-1/2 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Pre-diabetic.
Andere Medikamente: Metformain, magnesium malate, other supplements.
Allergien: Topical neomycin, molds.
Vorherige Impfungen: -

VAERS 2039362

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: MN
Alter: 46,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 13.11.2021
Beginn: 14.01.2022
Tage bis Beginn: 62,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Dyspnoea Exposure to SARS-CoV-2 SARS-CoV-2 test positive

Symptomtext

INCREASED SOB 1/13/22, LIKELY HOME EXPOSURE TO COVID BASED ON NOTES.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE COVID-19 PCR 1/14/22
Aktuelle Erkrankungen: -
Vorgeschichte: ILD 2/2 MCTD (on cyclophosphamide since 11/14), malnutrition/failure to thrive, iron deficiency anemia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1262095

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TN
Alter: 69,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 01.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: OT / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest pain Suicidal ideation

Symptomtext

INCREASED SUICIDAL THOUGHTS; This spontaneous report received from a patient concerned a 69 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: congestive heart disease, penicillin allergy, sulfa allergy, and oxycontin allergy. The patient previously received mrna 1273 (Moderna first dose, Dose number in series was 1) (form of admin, route of admin were not reported and batch number: 045A21A, expiry: UNKNOWN) dose was not reported, administered on 13-MAR-2021 for prophylactic vaccination. Patient did not get a second dose of Moderna. No adverse events reported after taking MRNA 1273 (Moderna First dose) (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series was 2) (suspension for injection, route of admin not reported, batch number: 1805025 expiry: 25-MAY-2021) dose was not reported, 1 total, administered on 20-MAR-2021 on left deltoid for prophylactic vaccination which was an off label use and inappropriate schedule of vaccine administered. Patient had chest pain following vaccination with first dose of covid-19 vaccine ad26.cov2.s (Dose number in series 2). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series was 3) (suspension for injection, intramuscular, batch number: 211A21A, and expiry: UNKNOWN) dose was not reported, 1 total, administered on 01-NOV-2021 on right deltoid for prophylactic vaccination. No concomitant medications were reported. On an unspecified date in DEC-2021, the patient had increased suicidal thoughts after receiving the booster, started in December and a little bit this month (January). The patient added that she had no plans of acting out these thoughts, did not own a gun, would not cut herself or was not planning to drive her car to hurt herself. It was confirmed with the patient that she had the ability to call emergency services if needed. The consumer stated that she has stopped having suicidal thoughts a couple of days ago (Dose number in series 3). The action taken with covid-19 vaccine ad26.cov2.s was not reported. The patient recovered from increased suicidal thoughts on JAN-2022. This report was serious (Other Medically Important Condition). This case, involving the same patient is linked to 20210426651.; Sender's Comments: V0: 20220110268-covid-19 vaccine ad26.cov2.s- increased suicidal thoughts. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergic reaction to antibiotics; Congestive heart failure; Drug allergy; Penicillin allergy
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2011248

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 40,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 29.09.2021
Beginn: 06.01.2022
Tage bis Beginn: 99,0
Dosis: N/A
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Laboratory test Magnetic resonance imaging Paraesthesia SARS-CoV-2 test positive Vertigo

Symptomtext

Vertigo and paresthesia occurred around 3 months after the mandated injection on 1/6/22 when I contracted COVID a second time. The first time I contracted COVID, prior to receiving the mandated vaccine, I only had flu-like symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -ER exam -Labwork -MRI -vertigo medication
Aktuelle Erkrankungen: COVID symptoms 1 month prior
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1999782

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: 59,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 09.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest pain Dysphagia Dyspnoea Laboratory test Mobility decreased SARS-CoV-2 test negative Sensation of foreign body

Symptomtext

The second dose enhanced the knot it my throat that I have had since the first dose. I have difficulty swallowing and putting my head down. I was having chest pains on 12/26/2021 and could not breathe so I went to the ER and tested negative for covid. They did a number of tests I can't remember.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure; migraines
Andere Medikamente: Atenolol; omeprazole; diclofenac
Allergien: Ibuprofen sensitivity
Vorherige Impfungen: Janssen dose 1 previous VAERS report completed for this dose.

VAERS 1997875

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Condition aggravated Diarrhoea Diarrhoea haemorrhagic Migraine Oropharyngeal pain Pain in extremity SARS-CoV-2 test negative Sinus congestion

Symptomtext

Developed Migraine head ache early the following day that lasted for 7 days, also stuffy sinuses and sore throat next day and lasting 3 days, and right calf pain to pinpoint spot 10/05/2021 through 10/08/2021, on 10/06/2021 passed bloody mucous bowel movement Tried taking my Rizatriptan for migraine on 2 of the 7 days with no relief. I reported all symptoms to my employer was given extra days off to recover and then cleared. They also had me get swabbed for Covid on 10/04/2021, which was negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: See above, Covid swab
Aktuelle Erkrankungen: None
Vorgeschichte: History of migraines , approximately 2-4 days per month, quickly relieved with Rizatriptan , constipation
Andere Medikamente: Calcium 600/ Vit d3 800 is, Vitex 1/3 rd capsule Monday, Wednesday, Friday, Amitiza 8 mg 2 times a day, Rizatriptan as needed for migraines
Allergien: None
Vorherige Impfungen: -

VAERS 1994776

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 35,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypertension Neuralgia Pain Pyrexia

Symptomtext

I have never had blood pressure issues before - developed hypertension about ~ 1-2 Weeks after taking the vaccine. Sometimes blood pressure is 150*100 which is extremely high and classified as hypertension. Prior to that, never had blood pressure higher than 130*85. The episodes of hypertension never stopped. Developed high fever (102.6 F) on the night of the vaccination that lasted for 2-3 Days. Developed aches throughout the body that seem like nerve pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: No medicines taken
Allergien: none
Vorherige Impfungen: -

VAERS 1975522

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 33,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 01.11.2021
Beginn: 10.12.2021
Tage bis Beginn: 39,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Burning sensation Hypertension Muscle twitching Pruritus

Symptomtext

I feel twitching most of the times and sometimes burning and itching feeling. Have high blood pressure sometimes. It?s started about a month of my vaccination. Before my vaccination never had problems.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1963486

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: -
Alter: 39,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Condition aggravated Throat tightness Urticaria

Symptomtext

hives, throat tightness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Factor V deficiency. Chronic urticaria, hydradenitis, asthma, adjustment disorder, anxiety,
Andere Medikamente: -
Allergien: avocado, budesonide, contrast medica, diazepam, dicyclomine, fexofenadine, fluticasone, hydromorphone, iodine, iopanoic acid, linezolid, nuts, shellfish
Vorherige Impfungen: influenza vaccine

VAERS 1957782

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: IN
Alter: 34,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: -
Beginn: 14.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Dyspnoea Headache Pyrexia Respiratory tract congestion

Symptomtext

CHEST CONGESTION; SHORTNESS OF BREATH; CHILLS; FEVER; HEADACHE ON THE RIGHT SIDE OF THE HEAD; This spontaneous report received from a patient concerned a 34 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry:14-DEC-2021) dose was not reported, administered on 14-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-DEC-2021, the patient experienced chest congestion. On 14-DEC-2021, the patient experienced shortness of breath. On 14-DEC-2021, the patient experienced chills. On 14-DEC-2021, the patient experienced fever. On 14-DEC-2021, the patient experienced headache on the right side of the head. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from chills, fever, chest congestion, shortness of breath, and headache on the right side of the head. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1936570

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CO
Alter: 53,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Adverse reaction Anxiety Blood test normal Fear Heart rate increased Heart rate irregular Hypertension Insomnia

Symptomtext

I have been experience rapid heartbeat, and irregular heartbeat since November 3rd, 2021. Varying degrees of intensity, causing trouble sleeping and great anxiety. My blood pressure is about 20pts higher than normal. My pulse is about 10-15 beats per minute higher than normal. My heart has been steady for my entire life, and I am quite frightened that the symptoms are permanent. The NP that I saw regarding this had not heard of such adverse reactions but it is listed on the CDC website as an adverse reaction to the J & J Janssen vaccine. My next step will be asking the NP for a referral to a cardiologist or internal medicine doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: General blood work was done, with no abnormal lab results. Item 21, I have checked Disability / permanent damage as a possibility. I do not know the outcome at this time.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 1936375

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CO
Alter: 38,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 30.09.2021
Beginn: 13.10.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood iron normal Blood thyroid stimulating hormone normal Dyspnoea exertional Exercise tolerance decreased Fibrin D dimer normal Full blood count normal Red blood cell sedimentation rate normal Troponin normal

Symptomtext

Early August '21 pt had fatigue for 3 days and his wife was sick for more than a week. Quarantined but never covid tested. he got the covid antibody test a few weeks later which was positive. Then got the Johnson & Johnson vaccine September 30 and a couple weeks later at Air Force Base shortly before PCS'ing to patient, noticed dyspnea on exertion about 14 or 15 minutes in the hard workout whereas usually can go 20 minutes or longer with no problem.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: CBC;Troponin; Iron Panel; TSH; ESR; D Dimer all wnl.
Aktuelle Erkrankungen: -
Vorgeschichte: denies; did test + for covid-19 antibodies in late August-- had fatigue x3 days several wks earlier.
Andere Medikamente: Denies.
Allergien: NKDA.
Vorherige Impfungen: -

VAERS 1913624

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: NV
Alter: 44,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood pressure increased Paraesthesia Swollen tongue

Symptomtext

tongue swelling, elevated blood pressure, tingling in arm and leg

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Zyrtec prn allergies
Allergien: Melons, almonds, pecans, pollen, dust, dander, mites, cats
Vorherige Impfungen: -

VAERS 1873776

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: NJ
Alter: 52,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Hypokinesia Injected limb mobility decreased Injection site pain

Symptomtext

LEFT SHOULDER PAIN; DIFFICULTY MOVING SHOULDER; This spontaneous report received from a health care professional concerned a 55 year old female of unknown ethnicity. The patient's height, and weight were not reported. The patient's concurrent conditions included diabetes mellitus, and hypertension. Also, patient never had adverse drug reaction following any previous vaccination. The patient was previously treated with covid-19 vaccine ad26. cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: unknown) dose, start therapy date were not reported, 1 in total for prophylactic vaccination. Patient experienced drug allergy when treated with levofloxacin. The patient received additional covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, intramuscular, batch number: 211A21A, and expiry: UNKNOWN) dose, start therapy date were not reported, 1 total, on left arm, for prophylactic vaccination (booster dose). Concomitant medications included Metformin, Metoprolol, and Ramipril. On an unspecified date, the patient experienced left shoulder pain, and difficulty moving shoulder continuing 4 days post vaccine. Patient is taking anti inflammatories, icing shoulder, and performing gentle range of motion stretches. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from left shoulder pain, and difficulty moving shoulder. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diabetes mellitus; Drug allergy (Levaquin); Hypertension
Vorgeschichte: Comments: Patient never had adverse drug reaction following any previous vaccination.
Andere Medikamente: METFORMIN; METOPROLOL; ALTACE
Allergien: -
Vorherige Impfungen: -

VAERS 1873776

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: NJ
Alter: 52,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Hypokinesia Injected limb mobility decreased Injection site pain

Symptomtext

LEFT SHOULDER PAIN; DIFFICULTY MOVING SHOULDER; This spontaneous report received from a health care professional concerned a 55 year old female of unknown ethnicity. The patient's height, and weight were not reported. The patient's concurrent conditions included diabetes mellitus, and hypertension. Also, patient never had adverse drug reaction following any previous vaccination. The patient was previously treated with covid-19 vaccine ad26. cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: unknown) dose, start therapy date were not reported, 1 in total for prophylactic vaccination. Patient experienced drug allergy when treated with levofloxacin. The patient received additional covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, intramuscular, batch number: 211A21A, and expiry: UNKNOWN) dose, start therapy date were not reported, 1 total, on left arm, for prophylactic vaccination (booster dose). Concomitant medications included Metformin, Metoprolol, and Ramipril. On an unspecified date, the patient experienced left shoulder pain, and difficulty moving shoulder continuing 4 days post vaccine. Patient is taking anti inflammatories, icing shoulder, and performing gentle range of motion stretches. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from left shoulder pain, and difficulty moving shoulder. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diabetes mellitus; Drug allergy (Levaquin); Hypertension
Vorgeschichte: Comments: Patient never had adverse drug reaction following any previous vaccination.
Andere Medikamente: METFORMIN; METOPROLOL; ALTACE
Allergien: -
Vorherige Impfungen: -

VAERS 1910451

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 27,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Confusional state Dyspnoea Headache Pain Pyrexia Urticaria Visual impairment Vomiting

Symptomtext

103 degree fever, shortness of breath, hives, decreased vision, headache, debilitating body pain, chest pain, vomiting, confusion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Pcn
Vorherige Impfungen: -

VAERS 1907139

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 30,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Activated partial thromboplastin time normal Alopecia Angiogram Angiogram normal Arthralgia Chest X-ray Chest pain Dysaesthesia Dyspnoea exertional Fibrin D dimer Full blood count normal Joint contracture Memory impairment Metabolic function test normal Muscle spasms Pain Pain in extremity Peripheral swelling

Symptomtext

4 hr post - "fire" in chest, Left hand contracture x2 days Throbbing pain moving up and down Right leg, back of calf, knee, thigh, described as "charley horse". Vomiting x2 weeks. Ongoing feet and lower leg swelling (R>L), exertional SOB, hair loss, decrease in short term memory, scalp dysesthesia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CBC, CMP, PT/PTT, Troponin, urinalysis - unremarkable. D-dimer 0.59 on 10/7/21 and 0.70 on 10/19/21 10/7/21 - CXR, LE DVT study, CT angiogram negative.
Aktuelle Erkrankungen: Recovered from Covid-19 illness starting 8/24/21
Vorgeschichte: Fibromyalgia, migraines, concussion (March 2021), epistaxis, tachycardia, anxiety
Andere Medikamente: Naratriptan, Sumatriptan, Polyethylene glycol, cyclobenzaprine, topiramate, diclofenac, omeprazole, Flovent 110mcg, Exedrin
Allergien: Succinylcholine
Vorherige Impfungen: -

VAERS 1837388

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: -
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: -
Beginn: 29.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Ageusia Anosmia Cough Diarrhoea Dyspnoea Angina pectoris Blood test COVID-19 Chest X-ray Chest discomfort Electrocardiogram Fibrin D dimer Laboratory test Lethargy Pain in extremity Eye pain Headache Hypersomnia

Symptomtext

CHEST WAS SQUEEZED; HEART PAIN; CONFIRMED COVID-19 INFECTION; VERY LETHARGIC; ARM PAIN; This spontaneous report received from a patient concerned a 28-year-old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: sulfa allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 211A21A expiry: UNKNOWN) dose was not reported, one total, administered at right arm on 28-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 28-OCT-2021, First before getting the vaccine patient did a Covid-19 test and it showed negative IgG (Immunoglobulin G (IgG)) and negative IgM (Immunoglobulin M (IgM)) and patient never tested positive for Covid infection in the past 20 months. Laboratory data included: Blood test (NR: not provided) Negative. On 29-OCT-2021, Patient started to experience normal stuffy nose, cough, sore throat, lethargic and arm pain (Pain in extremity). Patient was miserable until Sunday 31-OCT-2021. On 31-OCT-2021, patient noticed that he lost his taste and smell was gone. On 01-NOV-201 Monday morning, he had heart pain and shortness of breath that lasted until Wednesday 03-NOV-2021. Patient went urgent care where they did a rapid antigen test which came back as positive test. He had another Polymerase chain reaction (PCR) test on Thursday 04-NOV-2021 and it was also positive. The Polymerase chain reaction (PCR) was positive, while in Urgent care, they sent him for electrocardiogram (EKG) and it was abnormal. Patient went to emergency room (ER) from urgent care. They did several test. Patient did the D-dimer test and chest x-ray, all of that blood clots test, another EKG, troponin, blood test. Everything came back fine. He was discharged but until this day and he still had heart pain and shortness of breath. All other symptoms were gone except that he had no energy and he was very lethargic. He cannot exercise, he can only walk. Laboratory data included: COVID-19 antigen test (NR: not provided) Positive Covid infection, Chest X-ray (NR: not provided) Normal, EKG (NR: not provided) Normal, abnormal, Fibrin D dimer (NR: not provided) Normal, Laboratory test (NR: not provided) Normal, and Troponin (NR: not provided) Normal. On 04-NOV-2021, Laboratory data included: PCR (NR: not provided) Positive. On unspecified date, patient was on a plane and he felt like his chest was squeezed. He was not prescribed any medications. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from confirmed covid-19 infection, very lethargic, and heart pain, and the outcome of chest was squeezed and arm pain was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20211155211-COVID-19 VACCINE AD26.COV2.S-Heart pain. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20211028; Test Name: SARS-CoV-2 IgG antibody test; Result Unstructured Data: Negative; Test Date: 20211028; Test Name: Blood test; Result Unstructured Data: Negative; Test Date: 20211028; Test Name: SARS-CoV-2 IgM antibody test; Result Unstructured Data: Negative; Test Date: 20211103; Test Name: Laboratory test; Result Unstructured Data: Normal; Test Date: 20211103; Test Name: Troponin; Result Unstructured Data: Normal; Test Date: 20211103; Test Name: Chest X-ray; Result Unstructured Data: Normal; Test Date: 20211103; Test Name: EKG; Result Unstructured Data: Normal; Test Date: 20211103; Test Name: EKG; Result Unstructured Data: abnormal; Test Date: 20211103; Test Name: COVID-19 antigen test; Result Unstructured Data: Positive Covid infection; Test Date: 20211103; Test Name: Fibrin D dimer; Result Unstructured Data: Normal; Test Date: 20211104; Test Name: PCR; Result Unstructured Data: Positive
Aktuelle Erkrankungen: Allergic reaction to antibiotics
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1837388

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: -
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: -
Beginn: 29.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Ageusia Anosmia Cough Diarrhoea Dyspnoea Angina pectoris Blood test COVID-19 Chest X-ray Chest discomfort Electrocardiogram Fibrin D dimer Laboratory test Lethargy Pain in extremity Eye pain Headache Hypersomnia

Symptomtext

CHEST WAS SQUEEZED; HEART PAIN; CONFIRMED COVID-19 INFECTION; VERY LETHARGIC; ARM PAIN; This spontaneous report received from a patient concerned a 28-year-old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: sulfa allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 211A21A expiry: UNKNOWN) dose was not reported, one total, administered at right arm on 28-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 28-OCT-2021, First before getting the vaccine patient did a Covid-19 test and it showed negative IgG (Immunoglobulin G (IgG)) and negative IgM (Immunoglobulin M (IgM)) and patient never tested positive for Covid infection in the past 20 months. Laboratory data included: Blood test (NR: not provided) Negative. On 29-OCT-2021, Patient started to experience normal stuffy nose, cough, sore throat, lethargic and arm pain (Pain in extremity). Patient was miserable until Sunday 31-OCT-2021. On 31-OCT-2021, patient noticed that he lost his taste and smell was gone. On 01-NOV-201 Monday morning, he had heart pain and shortness of breath that lasted until Wednesday 03-NOV-2021. Patient went urgent care where they did a rapid antigen test which came back as positive test. He had another Polymerase chain reaction (PCR) test on Thursday 04-NOV-2021 and it was also positive. The Polymerase chain reaction (PCR) was positive, while in Urgent care, they sent him for electrocardiogram (EKG) and it was abnormal. Patient went to emergency room (ER) from urgent care. They did several test. Patient did the D-dimer test and chest x-ray, all of that blood clots test, another EKG, troponin, blood test. Everything came back fine. He was discharged but until this day and he still had heart pain and shortness of breath. All other symptoms were gone except that he had no energy and he was very lethargic. He cannot exercise, he can only walk. Laboratory data included: COVID-19 antigen test (NR: not provided) Positive Covid infection, Chest X-ray (NR: not provided) Normal, EKG (NR: not provided) Normal, abnormal, Fibrin D dimer (NR: not provided) Normal, Laboratory test (NR: not provided) Normal, and Troponin (NR: not provided) Normal. On 04-NOV-2021, Laboratory data included: PCR (NR: not provided) Positive. On unspecified date, patient was on a plane and he felt like his chest was squeezed. He was not prescribed any medications. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from confirmed covid-19 infection, very lethargic, and heart pain, and the outcome of chest was squeezed and arm pain was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20211155211-COVID-19 VACCINE AD26.COV2.S-Heart pain. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20211028; Test Name: SARS-CoV-2 IgG antibody test; Result Unstructured Data: Negative; Test Date: 20211028; Test Name: Blood test; Result Unstructured Data: Negative; Test Date: 20211028; Test Name: SARS-CoV-2 IgM antibody test; Result Unstructured Data: Negative; Test Date: 20211103; Test Name: Laboratory test; Result Unstructured Data: Normal; Test Date: 20211103; Test Name: Troponin; Result Unstructured Data: Normal; Test Date: 20211103; Test Name: Chest X-ray; Result Unstructured Data: Normal; Test Date: 20211103; Test Name: EKG; Result Unstructured Data: Normal; Test Date: 20211103; Test Name: EKG; Result Unstructured Data: abnormal; Test Date: 20211103; Test Name: COVID-19 antigen test; Result Unstructured Data: Positive Covid infection; Test Date: 20211103; Test Name: Fibrin D dimer; Result Unstructured Data: Normal; Test Date: 20211104; Test Name: PCR; Result Unstructured Data: Positive
Aktuelle Erkrankungen: Allergic reaction to antibiotics
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1888841

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A 21A

moderat

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 21.11.2021
Impfdatum: 29.09.2021
Beginn: 21.10.2021
Tage bis Beginn: 22,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Diplopia Hypoaesthesia Paraesthesia

Symptomtext

Tingling and numbness in fingers on left hand and arm areas. Double vision started in right side though has now progressed to left eye also.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None ..havent gone to Doctor.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1881227

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WI
Alter: 55,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 08.10.2021
Beginn: 07.11.2021
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Electromyogram Hypoaesthesia Paraesthesia

Symptomtext

Numbness and tingling

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: EMG
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1880430

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: NY
Alter: 27,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Tremor

Symptomtext

Pt woke up at 2am violently "shaking" for 15-20mins

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Pt was referred to the urgent care/ER
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1873513

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: 38,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Paraesthesia Throat irritation

Symptomtext

PT recvd Janssen Booster and begin to feel tingling to bilateral lower leg, thighs and reported itchy throat. Provider administered Benadryl 25mg PoX1 12:50PM. After 5mins patient felt better and symptoms resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: BP: 132/69 HR: 88 RR: 16 Sat: 98%
Aktuelle Erkrankungen: N/A
Vorgeschichte: HTN
Andere Medikamente: Lisinopril
Allergien: NKA
Vorherige Impfungen: -

VAERS 1870930

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CO
Alter: 39,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Bedridden Dizziness Dyspnoea Feeding disorder Headache Loss of personal independence in daily activities Peripheral swelling Pharyngeal swelling Pyrexia Vision blurred

Symptomtext

Swelling of throat and unable to eat for 48 hrs, blurred vision, fever ~ 102?F, swelling of hands/arms and feet/legs, headache, bedridden, dizzy spells during the first 4 days. Ongoing for 9 weeks, shortness of breath and unable to return to daily activities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Scheduled for chest X-ray, pulmonary function test, CT scan
Aktuelle Erkrankungen: None
Vorgeschichte: None prior to vaccination
Andere Medikamente: Multivitamin
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1867938

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: 43,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 07.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 28,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Palpitations

Symptomtext

Palpitations on and off

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None yet, no insurance.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tylenol
Allergien: Na
Vorherige Impfungen: -

VAERS 1865707

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 12.11.2021
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: unbekannt Erholt: nein

Chest pain Discomfort Eye discharge Eye pruritus Eye swelling Fatigue Feeling hot Headache Hypersensitivity Impaired work ability Injection site swelling Lip swelling Mouth swelling Pain Pain in extremity Pruritus Pyrexia Swelling face

Symptomtext

Thursday , After getting shot, I went home. Started feeling warm inside, then some itchy feelings. Headache within a couple hours . Took tylenol for the headache. That night was very uncomfortable with fever and some ache's and hot inside and outside. by morning left side was VERY sore on arm and walnut size where shot given. Face and eyes started swelling up , then my mouth inside and lips. Took a couple benedryl. Eyes were very goopy and swollen. Took Benedryl all weekend. Still had swelling on Monday. took that day off from work also. Felt like a reaction when i have had shellfish or iodine. If the swelling had got worse, was going to go to hospital , but the benedryl was working. Eyes even today , goopy and itch feeling still on body....still seem more tired than usual. some chest pains and arms on occasion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: back pain chronic
Andere Medikamente: multi vitamin, mobic
Allergien: Iodine , shellfish, sulfa antibiotics, certain soaps and laundry detergent
Vorherige Impfungen: -

VAERS 1865361

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 60,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 21.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood albumin normal Blood alcohol normal Blood alkaline phosphatase increased Blood bilirubin increased Blood calcium normal Blood chloride decreased Blood creatinine increased Blood glucose increased Blood lactic acid Blood sodium decreased Blood urea increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Differential white blood cell count abnormal Dizziness Drug screen negative Full blood count abnormal

Symptomtext

Patient felt ill around 4:00 a.m. morning after getting shot with nausea and dizziness. He continued to be vaguely ill until 10/20/21 when he lost muscle control, had shakiness, fever (v to 102.5+), nausea. E.R. determined he with Covid Viral Pneumonia, with low oxygen levels and abnormal chest x-rays; treated in ER with promethazine, sodium choride 0.9% and oxygen. He was admitted him to hospital. Treatment included Remdesivir, dexamethasone, and magnesium

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: LABS Labs Reviewed INFLUENZA A,B,COVID-19,NAAT - Abnormal; Notable for the following components: Result Value SARS-CoV-2, NAAT (COVID-19) Detected (*) All other components within normal limits CBC WITH DIFFERENTIAL - Abnormal; Notable for the following components: % Lymphocytes 16.5 (*) % Immature Granulocytes 0.6 (*) Absolute Immature Granulocytes 0.05 (*) All other components within normal limits COMPREHENSIVE METABOLIC PANEL - Abnormal; Notable for the following components: Na 133 (*) Cl 95 (*) Glucose 245 (*) BUN 29 (*) Creatinine 2.07 (*) eGFR, non-African American 33 (*) eGFR, African American 40 (*) Calcium 10.5 (*) Albumin 4.9 (*) Bilirubin Total 1.4 (*) Alkaline Phosphatase 208 (*) All other components within normal limits LACTIC ACID - Abnormal; Notable for the following components: Lactate 3.5 (*) All other components within normal limits URINALYSIS WITH MICROSCOPIC - Abnormal; Notable for the following components: Specific Gravity, Urine 1.045 (*) Glucose, Urine 150 mg/dL (*) Mucus, Urine Present (*) Hyaline Casts, Urine 5-10 (*) All other components within normal limits ALCOHOL - Normal DRUGS OF ABUSE, SCREEN, URINE
Aktuelle Erkrankungen: none
Vorgeschichte: anxiety, diabetes
Andere Medikamente: blood pressure med, cholesterol med, anxiety med, diabetes med
Allergien: none
Vorherige Impfungen: -

VAERS 1858497

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: LA
Alter: 58,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 07.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Headache

Symptomtext

I had headaches most of my life since junior high. 2 days post vaccine, 10/09/2021, headaches were different and did not respond as well to medication. They were more frequent and stabilized a little bit a week later. 10/15/2021, they still did not respond to my normal taking the medications. Now they are more frequent prior to the vaccine, but I can still manage them. I self-managed the headaches. On 11/03/2021, when I was on military orders, I took the flu vaccine, and the headaches became significantly worse on 11/04/2021. On11/05/2021, I went to talk to one of the doctor's suite surgeons office. The doctor gave me 400 mg of Ibuprofen. The flu vaccine coupled with the J&J, I wasn't sure if it was an interaction with both vaccines that caused my headaches to become worse, because I never had an adverse reaction to the flu vaccine in the 20 years in the military. I still get the headaches, but it went back to the consistency to the post J&J vaccine headaches. Not back to what I normally deal with.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Sleep Apnea
Andere Medikamente: Ibuprofen 200 mg Tylenol 250 mg 250 mg aspirin 65 mg caffeine
Allergien: N/A
Vorherige Impfungen: Nothing other than expected from flu vaccine and yellow fever

VAERS 1857605

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

moderat

Staat: FL
Alter: 57,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 14.09.2021
Beginn: 18.10.2021
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Headache Hypoaesthesia Nausea Paraesthesia Vision blurred

Symptomtext

Patient complains of sudden onset of numbness/tingling and weakness to "random" extremities of his body for past 3 weeks. Currently his right arm/shoulder is tingling and numb but it tends to disappear and reappear in a different part of his body. Patient also reports he has been having headaches - occipital and temporal -- for the last 2-3 weeks accompanied by nausea. Headaches last for about 45 minutes to an hour and then they disappear. Nausea appears with the headaches. Denies and aura. Patient also complains of "random" blurry vision. All of these symptoms have started acutely about 2-3 weeks ago. Patient denies dizziness, slurred speech, trouble speaking, changes in balance or gait. Patient refused an ambulance at time of visit. Advised patient to go to the Emergency Department.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1852238

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 29.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain Tachycardia

Symptomtext

Answered phone and someone began talking about suspected adverse reaction to vaccine administered, stating she had texted a number that asked her about vaccine side affects that failed to respond to her. I asked to verify ID and led to patients chart. Client then said she wanted it reported that she had adverse affects. She reported that she has "terrible throbbing pain in head and neck and legs, and rapid heart beat". I told her to go to hospital or call 911 if she cannot make it to the hospital. She demanded I take note of her symptoms which I was in her EHR. I stated again that these symptoms sound worrying and she should go to the hospital right away. continued on next page... She questioned if I was taking note of her symptoms, I assured the patient I was noting what she told me and emphasized due to her symptoms she should see a doctor right away. She then stated she wanted us to report this so 'her attorney could reference it'. I told her she needs to be examined by a doctor immediately, she stated 'she will see her own doctor virtually'. Made clear point to go to emergency room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Urged to go to hospital immediately, RE: Rapid heart rate and throbbing pains
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1850014

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: NV
Alter: 55,0
Geschlecht: F
Eingang: 08.11.2021
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: nein

Injection site pain Joint range of motion decreased Mobility decreased Muscular weakness Myalgia

Symptomtext

left deltoid disabling pain and use of muscle, decreased abduction of shoulder and arm. Tenderness over injection site, decreased range of motion with progressive weakness in left arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: hypotyroid
Andere Medikamente: progesterone, spironolactone, armour thyroid
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1848916

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: AL
Alter: 26,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Abdominal pain upper Asthenia Back pain Chest discomfort Chills Dizziness Dizziness postural Dyspnoea Erythema Feeling abnormal Gait disturbance Headache Heart rate increased Muscle tightness Myalgia Pain in extremity Pyrexia Sleep disorder

Symptomtext

Felt fine all day after the vaccine, about 12 hours later I started feeling bad very quickly. Fever, chills, headache, uncontrollable shivering, difficulty walking and breathing due to back pain and clenching of muscles, tried to sleep it off but woke up a few hours later from a sharp pain in my head. Alarmingly I found my face was red and swollen, I was very weak, and had difficulty breathing, my legs and chest felt tight, my headache was very severe. I had a fever of 102.1 F. I was very dizzy especially when laying down and had a slight ringing in my ears. I had shortness of breathe and some stomach pain. I tried to decide weather or not to call an ambulance since I live alone. I took 2000 mg of Tylenol and waited. My symptoms started to decrease after 2 hours and I drove to the hospital. They monitored my vitals for 3 more hours as my symptoms continued to decrease. I left feeling weak and shivery, with muscle soreness and dizziness around 7:00 am. Day 2 I had a headache and fever off around 99-101, and dizziness. Mild dizziness and soreness in my arm continued for the next week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Monitoring of vitals. Blood pressure was ok. Fever and heart rate decreased as symptoms went down
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D3 with K2 5000 IU
Allergien: None
Vorherige Impfungen: -

VAERS 1845258

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: IN
Alter: 34,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: -
Beginn: 02.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Bone pain Chest discomfort Dizziness Dyspnoea Fatigue Feeling abnormal Feeling cold Headache Hyperhidrosis Influenza like illness Nasal congestion Night sweats Oral pain Pain Pain in extremity Pyrexia

Symptomtext

FEEL COLD; HANDS AND HEAD ARE SWEATING; LIKE SOMEONE SITTING ON CHEST; FEELS LIKE GOT HIT BY A DAMN TRUCK; ARM HURTS LIKE HELL; HEADACHE ON AND OFF; FEVER; TIRED; BODY ACHES; BONES HURT; MOUTH HURTS; DIZZINESS / WOOZY; PRETTY EXTREME LIKE A BAD FLU/FEEL SICK; FEELS LIKE CLOGGED NOSE; HARD TO TAKE DEEP BREATH; WOKE UP IN MIDDLE OF NIGHT SWEATING; This spontaneous report received from a patient concerned a 34 year old male. The patient's height, and weight were not reported. The patient's past medical history included: covid-19, and other pre-existing medical conditions included: No known medical history. The patient's grandfather died of aneurysm. Headaches come and go and really bad last night. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, administered on 02-NOV-2021 14:30 for prophylactic vaccination. No concomitant medications were reported. On 02-NOV-2021, the patient experienced body aches. On 02-NOV-2021, the patient experienced bones hurt. On 02-NOV-2021, the patient experienced mouth hurts. On 02-NOV-2021, the patient experienced dizziness / woozy. On 02-NOV-2021, the patient experienced pretty extreme like a bad flu/feel sick. On 02-NOV-2021, the patient experienced feels like clogged nose. On 02-NOV-2021, the patient experienced hard to take deep breath. On 02-NOV-2021, the patient experienced woke up in middle of night sweating. On 02-NOV-2021, the patient experienced feels like got hit by a damn truck. On 02-NOV-2021, the patient experienced arm hurts like hell. On 02-NOV-2021, the patient experienced headache on and off. On 02-NOV-2021, the patient experienced fever. On 02-NOV-2021, the patient experienced tired. On 03-NOV-2021, the patient experienced hands and head are sweating. On 03-NOV-2021, the patient experienced like someone sitting on chest. On 03-NOV-2021, the patient experienced feel cold. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from body aches, tired, fever, bones hurt, mouth hurts, dizziness / woozy, arm hurts like hell, pretty extreme like a bad flu/feel sick, feels like clogged nose, hard to take deep breath, headache on and off, feel cold, hands and head are sweating, and like someone sitting on chest, and the outcome of woke up in middle of night sweating and feels like got hit by a damn truck was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Comments: No known medical history. The patient's grandfather died of aneurysm. Headaches come and go and really bad last night.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1844034

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

moderat

Staat: WA
Alter: 47,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 28.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arrhythmia Arthralgia Dyspnoea Fatigue Headache Hot flush Immediate post-injection reaction Tendonitis Tinnitus

Symptomtext

Immediately flush, hot, tired. Later on, after about 1 week, joint pain, tendonitis, headache, tinnitus in left ear which all persist. I had COVID in May 2021. Most concerning is some kind of positional arrhythmia when I lay down, which seemed to start a few weeks after IM. Vaccinologist did not aspirate the needle as I asked. Still have frequent headaches, joint pain, get out of breath easily, and the arrhythmia. Getting doctor's appt.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: upcoming
Aktuelle Erkrankungen: na
Vorgeschichte: na
Andere Medikamente: na
Allergien: na
Vorherige Impfungen: -

VAERS 1843779

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: 46,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Dizziness Feeling hot Heart rate decreased Hypoaesthesia Pallor Paraesthesia

Symptomtext

1500 injection. 1508 began to feel dizziness, tingling in hands, warmth and numbness, pulsed dropped to 50 color pale, vitals 135/115 has not had anything to eat since 9am

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: depression/anxiety
Vorgeschichte: -
Andere Medikamente: Sertraline 50mg
Allergien: none known
Vorherige Impfungen: -

VAERS 1842367

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 07.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Dizziness Electrocardiogram Heart rate increased Musculoskeletal stiffness Palpitations Paraesthesia Tinnitus

Symptomtext

Immediate neck stiffness and woke up 12 hours later with pounding heart and ringing and pounding in ears, tingling hands and feet and light headedness This continued for a week. The lightheadedness subsided after one week but ringing and pounding in ears remains. Resting heart rate remains elevated as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG and blood work
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1842353

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CO
Alter: 35,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 23.09.2021
Beginn: 23.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Headache Heart rate increased Injection site discomfort Injection site pain Limb discomfort Pain Pain in extremity Paraesthesia oral

Symptomtext

Headache (7 days) Tingling sensation on bottom lip (1 day) Pain/Soreness at injection site (5 days) Pain/discomfort from injection site down to my hand (3-5 days) Fatigue (3-5 days) Slight body aches (3-5 days) Elevated heart rate (1-2 days)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Severe cat dander allergies
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1830617

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WI
Alter: 34,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain Asthenia Back pain Chest pain Chills Diarrhoea Dizziness Dyspnoea Epistaxis Fatigue Feeling abnormal Headache Hyperhidrosis Lethargy Muscle twitching Nausea Pain Pain in extremity

Symptomtext

1700- Dizziness, Headache, Sweating, Tachypnea By 2000 - Headache, Body Aches, Fatigue, Abdominal Pain, Muscle Twinges, Chills, Rigors, Fever 101 F- with Acetaminophen and Ibuprofen, Chest Pain, SOB, Weakness, Arm Pain, Nausea, Runny Nose Day Two - Lethargy, Headache, Fever, Body Aches, SOB, Calf Pain, Abdominal Pain, Nausea Day Three - Abdominal Pain, Muscle Twinges, Nose Bleed, Calf Pain, Lethargy, Headache, Arm Pain, SOB, Back Pain, Ears Ringing Day Four - Diarrhea, Abdominal Pain, Calf Pain, Weakness, Muscle Twinges, Arm Pain, Fatigue - Brain Fog?, SOB, Headache, Back Pain ...... Onto Day 9 (Current Day) - Calf Pain, Muscle Twinges, Headache, Arm Pain, Weakness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Allergies
Andere Medikamente: Allegra, Pepcid
Allergien: Amoxicillin, Cats, Seasonal Allergies
Vorherige Impfungen: -

VAERS 1829345

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: MT
Alter: 42,0
Geschlecht: M
Eingang: 29.10.2021
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: nein

Chest pain Fall Fatigue Feeling hot Pain in extremity

Symptomtext

Patient reports on 10/13/2021 at approximately 11:30 pm patient was laying in bed. He reports he started to feel hot and went out to his chair in the living room. Patient was sitting in chair when his left arm had extreme pain and then severe chest pain began. Patient reports he fell to his knees and was unable to call out to his spouse for approximately two minutes after chest pain started. Patient reports "I thought my heart was going to explode". Patient reports the pain subsided after a couple of minutes. He denies no further symptoms of chest pain but does report continued left arm pain and fatigue since this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None reported
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: none reported
Allergien: NKDA reported
Vorherige Impfungen: -

VAERS 1828881

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

moderat

Staat: WA
Alter: 36,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 28.09.2021
Beginn: 02.10.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Hypoaesthesia Injection site mass Injection site pain Injection site pruritus Injection site swelling Injection site warmth Pain in extremity Paraesthesia

Symptomtext

Saturday I had a sore arm. Felt burning, itching, hot on skin of upper left arm. Felt a large lump. Two days later felt another burning, hot itching bump a few inches down. Felt swollen. From 24 hours of the vaccine both arms were numb and tingly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Urgent care visit 10/8 when skin irritations and numbness wouldn't go away. Received medication (antibiotics and steroids) for cysts that had developed.
Aktuelle Erkrankungen: Covid-19
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxine
Allergien: -
Vorherige Impfungen: -

VAERS 1822180

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: 45,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthma Condition aggravated Cough Paraesthesia oral Pharyngeal paraesthesia

Symptomtext

Client was vaccinated at 1500, ad while in observation she reported having tingling in mouth, throat, and cough. She described it as asthma attach. PN and EMS attended her at 1526. VS: 168/81, Res 24, Pulse 115, Ox 98%. Patient was administered Benadryl 25mg at 1530. Client reported not to feel the above feelings. She signed the refusal to transport. Released at 1600. She felt awake and fine before her vials taken and released. 145/84, pulse 104, Ox 99%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, Allergies, HTN
Andere Medikamente: Albuterol PRN, Flonase, Claritin, Losartan HCTZ
Allergien: Shelfish, Arythromicin-anaphylaxis
Vorherige Impfungen: -

VAERS 1818708

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: 42,0
Geschlecht: M
Eingang: 26.10.2021
Impfdatum: 27.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Grip strength decreased Injection site pain Mobility decreased Neck pain Pain Pain in extremity

Symptomtext

Continous Pain at site of Vaccine. even after 30 days, acute pain at vaccine site. pain radiating from point of Vaccination an dtravelling up to left side shoulder and neck. and down to elbow and forearm. reduced grip and weight lifing ability in Left arm, along with pain for any grip or lift actions

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: None
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 1818187

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: MN
Alter: 44,0
Geschlecht: M
Eingang: 26.10.2021
Impfdatum: 22.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fibrin D dimer Formication Full blood count normal Hypoaesthesia Metabolic function test Paraesthesia Prothrombin level normal Sensory loss

Symptomtext

About 1 week in started to get numbness and tingling in hands and feet. On the 2 week mark my forearms and calves were constantly "crawling" with a tingling sensation. Noticed finger tips could no longer feel extreme heat or cold. Saw Dr. fearful of clot issues, but he advised it would not be in all four extremities and then asked if I saw the other J&J side effect of GBS. I did not see the August reports of "about 100" with this side effect. I lived the next 2 weeks in fear would this progress. Thankful now I'm 5 weeks out and my forearms and calves are back to normal, but hands and feel remain agitated with less sensation and the tingle sensation coming and going. This never happened to me before the J&J shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 10/5 - 2 weeks after saw Dr. D-Dimer, Prothrombin, Complete Blood count, Extended Metabolic profile - All came back normal, D-Dimer <220 This proved it was nothing clot related. At that point Dr. advised on GBS possibility and to be watchful for symptoms.
Aktuelle Erkrankungen: none at time, COVID positive on July 29th - better in 3-4 days
Vorgeschichte: none
Andere Medikamente: Vitamin D 5000 IU/day, multivitamin, Allegra-D 24 hour
Allergien: none
Vorherige Impfungen: -

VAERS 1815155

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

moderat

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Decreased appetite Diarrhoea Fatigue Nausea Pyrexia Rash Tachycardia

Symptomtext

tachycardia, fever chills chest rash nausea diarrhea extreme fatigue loss of appetite

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: htn
Andere Medikamente: triam/hctz amlodipine baby asprin
Allergien: pcn sulfonamides
Vorherige Impfungen: -

VAERS 1795433

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

moderat

Staat: OH
Alter: 43,0
Geschlecht: F
Eingang: 25.10.2021
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: nein

Anxiety Chills Nervousness Blood pressure increased Blood test Burning sensation Chest X-ray Dizziness Dyspnoea Electrocardiogram Fatigue Heart rate increased Hyperhidrosis Immediate post-injection reaction Impaired work ability Mobility decreased Nausea Pain

Symptomtext

patient extremely anxious about getting vaccine prior to administration on 10/12/2021. patient anxiety continued following administration of vaccine. reported feeling nervous, chills, and general anxiety. patient left pharmacy approximately 30 minutes after vaccination, accompanied by her spouse. established contact with primary care physician.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: next contact from patient, received telephone call from her on 10/25/21. reported that she had been improving. she did visit with primary care physician on 3 occasions. primary care prescriber treated her for fever, and related symptoms, and completed VAERS REPORT #683460.
Aktuelle Erkrankungen: none known
Vorgeschichte: none known
Andere Medikamente: none known
Allergien: no known drug allergies
Vorherige Impfungen: -

VAERS 1809371

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

moderat

Staat: AZ
Alter: 60,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 04.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Fatigue Hypoaesthesia Migraine Nausea Pyrexia

Symptomtext

Fever, chills, migraine headache, fatigue, numbness in left leg from knee to foot, nausea. Symptoms lasted for 8 days before subsiding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Weak immune system
Andere Medikamente: Wellbutrin, Estrodiol Patch, Progesterone
Allergien: Erethomyacin
Vorherige Impfungen: -

VAERS 1809002

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21a

moderat

Staat: WA
Alter: 44,0
Geschlecht: F
Eingang: 22.10.2021
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: nein

Migraine Vomiting

Symptomtext

Hyperemesis x 6 days Migraine .. since injection non stop

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tylenol Omeprazole
Allergien: NKMA
Vorherige Impfungen: -

VAERS 1808021

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: 30,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Hypoaesthesia Pain in extremity Paraesthesia Skin warm

Symptomtext

PT 30y female on site rec'd J&J vaccine @ 10:20AM to L arm. Went to observation and started to feel tingling and pain with itching to L arm at 10:30AM. RN assessed PT and notified NP. NP and PT was given 25mg of Benedryl @10:35am pt denies any SOB, face tightness, chest pain, claudication, arm weakness. NP @ site stated that PT stated that numbness and tingling felt like it was improving , extremities warm to the touch , pulse present and bounding. Strength equal throughout upper extremities , no hives, rash, bruising noted @10:46am. PT starts to c/o feeling a different type of pain to L arm it feels like scraping of my bone and I feel lightheaded. NP gave 0.3mg of Epi to LL thigh, EMS on site and Pt transported @ loss to hospital at this time pt stated that she has no one to pick up her car.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: BP 100/80, 20RR, 72 pulse , 99.7 temp
Aktuelle Erkrankungen: None
Vorgeschichte: N/A
Andere Medikamente: None
Allergien: Ibuprofen
Vorherige Impfungen: -

VAERS 1797840

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: KS
Alter: 32,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 01.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Angina pectoris Blood test Chills Electrocardiogram Fatigue Headache Hot flush Irritability Mobility decreased Musculoskeletal pain Nausea Pain in extremity Ultrasound scan

Symptomtext

Pt. states that after receiving the 1st dose of J&J 10/01/2021, started experiencing symptoms 10/04/2021 of fatigue, nausea, severe headache (lasting a week), hot flashes, chills, irritability, random pain in both legs, severe pain from the back of shoulder blades to the back of the head. Physical Therapist visit 10/14/2021 loss of right shoulder mobility/Tension. 10/07/2021 Primary visit prescribed Zofran for nausea, continuing to experience symptoms of "heart pain" 10/10/2021 Hospital visit/ EKG, Blood Work, and Ultrasound. 10/18/2021 Blood Work , recommendation of PT *Shoulder Mobility, and observation. Still experiencing symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: EKG 10/10/2021 Blood Work 10/10/2021 Ultrasound 10/10/2021 Blood Work 10/18/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: Tumor in the Head
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1796344

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: MT
Alter: 30,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Cardiac monitoring Chest pain Chills Headache Migraine Pyrexia Vomiting

Symptomtext

4 hours after headache started. 10 hours severe headache/migraine. 14 hours after vomiting, fever, chills, weakness, body aches. 24 hours after headache, fever, chills, weakness continued. 48 hours after headache continued, noticed slight chest pain. 50 hours after chest pain worsened. 54 hours after chest pain seemed to go away. One week after and still have chest pain on and off throughout the day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 10/9/21 was hooked up to monitor at time of chest pains diminishing, normal heart rate and blood pressure observed.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1795465

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain Dizziness Dyspnoea Headache Nausea Pain Rash Swollen tongue

Symptomtext

Severe headaches, rash on arm, shortness of breath, dizziness, nausea, tongue began to swell, body ache, abdominal pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Crohn's disease.
Andere Medikamente: None.
Allergien: Flu-vaccine.
Vorherige Impfungen: Flu vaccine

VAERS 1795249

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CO
Alter: 38,0
Geschlecht: F
Eingang: 18.10.2021
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: ja Erholt: nein

Anxiety Crying Dizziness Dysstasia Hyperhidrosis Muscle tightness Nausea Pallor Tremor

Symptomtext

Client presented to clinic for Janssen's COVID-19 vaccine with her husband. Client appeared anxious and had multiple questions about the safety and efficacy of the vaccine prior to administration. Client stated she was being required to have the vaccine and was not happy about it and was very nervous. Client cried briefly and reported that her heart rate felt 'fast' due to anxiety. Client ceased crying, reported that her questions were answered, and consented to the vaccine. COVID-19 Janssen was administered at 10:25am. At 10:28am, client reported feeling dizzy, lightheaded, nauseous and was visibly pale and diaphoretic. Client was lowered safely to the ground with the help of her husband. Within 20 seconds, the client began to feel better and pallor had diminished. Client reported that she had passed out during a blood draw previously, but never problems with vaccine. Client slowly resumed a sitting position and returned to a chair. Client declined juice, but drank water and reported feeling much better. At about 10:38, client again felt faint, was pale and diaphoretic and was lowered to the ground. Client stated that the muscles in her neck, near her throat, felt tight, but anxiety related. Client denied problems breathing or sensation of swelling in throat or mouth. No hives were present. Client was given a cold compress, snack and juice and reported that the tight muscles in her neck had gone away. Client reported feeling better and resumed sitting in chair. Client was making conversation, but at about 10:55am, client reported feeling faint and was moved to the ground. At this time, additional nursing staff were called in. Client reported that the tightness in her neck had returned and she was still feeling lightheaded. Client denied symptoms of anaphylaxis, reported no problems breathing. Informed the client's husband that we advised EMS services due to delayed recovery. The client began to cry and shake uncontrollably. Monitored the client on the ground while we called 911 at 11:00am. EMS arrived at 11:05am and assessed the client for about 15 minutes. Vital signs and EKG were all normal. No signs of anaphylaxis. Client continued to feel dizzy, appeared diaphoretic and pale, and could not stop shaking. Client was advised to seek medical treatment as a precaution and to be monitored. Client was unable to stand unassisted due to lightheadedness when standing. Client was transported via ambulance to Hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1793672

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 40,0
Geschlecht: M
Eingang: 16.10.2021
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Asthenia Mobility decreased

Symptomtext

Shortly after the injection, I was experiencing shoulder pain and reduced mobility. I didn't think much about it, assumed it would go away. Over the last 4 days, the pain, weakening and reduced mobility have progressively increased. I have taken OTC pain medication and anti-inflammatory meds.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Vitamin C, Vitamin D, Zinc, occasional Excedrin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1788761

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 30,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 04.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test normal Chest discomfort Chest pain Dizziness Electrocardiogram normal Feeling drunk Headache Pain in extremity Painful respiration Sleep disorder Tension headache X-ray normal

Symptomtext

Monday after I received the vaccine I started feeling the arm soreness which I was expecting. I was getting headaches, but it wasn't super painful. It was manageable as expected. On Tuesday night, I had an episode where I was getting chest pressure and light headed. And I had severe tension headaches in front and back of head. Wednesday it was tension headaches, lightheadedness. The best way I can describe it is being tipsy. So moving losing some coordination but still being able to walk and function. On Thursday was when I started feeling pressure on my chest and tension headaches. I was also starting to feel pain in the left and right sides of my chest. On Saturday I went to work (active) 9am-10pm. around 10:30 am I started to feel lightheaded and stepped outside, I was outside for about 15 minutes. I felt like I was gonna pass out and I decided to go into the museum. If I passed out someone would find me there. I went back inside and sat down and drank water. And same thing as Tuesday night I waited for it to pass. I was the senior technician there and worked through then went to the hospital at 6:30pm after work. So I was at the ER until 10:30pm. Blood work, x-rays, EKG, BP, everything came back normal. I was prescribed with over the counter ibuprofen 200mg every 6-8 hours with meals. My diagnosis was uncertain cause of chest pain. I ended up getting a doctor's note for the rest of the week (Saturday 10/9). And then on Monday I got another appointment at a HCF because the chest pain would subside and then I have episodes where it's a very sharp stabbing pain throughout my chest as well as pressure. And I was told after taking pain killers that it would subside. I was prescribed to take 600mg of ibuprofen every 6 hours prescribed on 10/11 (Monday). I've just been having pain pressure on my chest. The pain after medication is manageable. I cant be on certain positions when I sleep and it gives me more pain. Usually around the time I take medication, I get a pain flare off. Sometimes I have to take medication earlier than 6 hours. And it's extreme. And now it's more located on the left side in between my breasts. I did have another check up over the phone today 10/15. I asked for another set of x-rays and I was just told to take Tylenol in between the ibuprofen. Other than that I was just told to wait for it subside. Still ongoing. I've also noticed that the pain happens when I'm breathing. When I breathe in, it's the sharpest, when I hold it in, there's no pain. When I breathe out, it's milder than breathing in.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Blood work 10/9/21, blood clot test 10/9/21, 10/11/21, X-rays 10/9/21, EKG 10/9/21, BP 10/9/21, 10/11/21, (all came back normal).
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A; ibuprofen as needed
Allergien: Amoxicillin; environmental allergies
Vorherige Impfungen: -

VAERS 1788161

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 50,0
Geschlecht: M
Eingang: 15.10.2021
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain Abdominal pain upper Blood test Chest X-ray Dyspnoea Ear discomfort Headache Pain Paranasal sinus discomfort Tinnitus

Symptomtext

Severe head ache, severe pressure in sinus/ears, severe ringing in the ears, severe body pain/ache, upper abdominal pain/cramping, slight breathing constriction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: blood test 10/5/21, chest x-ray 10/5/21.
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic Pain, Asthma, Celiac Disease
Andere Medikamente: SPIRIVA; FLONASE; VIANTEROL; LEVALBUTEROL; XTAMPZA; TRAMADOL; SINGULAIR; VITAMIN D3; ZINC
Allergien: Flu Vaccine, Cipro, NSAIDS, wheat, eggs
Vorherige Impfungen: October 2019 flu vaccine.

VAERS 1785471

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 47,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 01.10.2021
Beginn: 02.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Blood pressure increased Chills Paraesthesia Pyrexia Vomiting

Symptomtext

After the initial fever, chills and vomiting for two day after shot, I now have weird tingling under my skin across my entire back. Almost like their is something crawling around under my skin. Sometimes that feeling extends to shoulders and hips. I feel weak most of the day. My blood pressure is more elevated than normal. It has been 14 days since the shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Seasonal cold 4 weeks prior.
Vorgeschichte: High blood pressure. Treated with benazapril.
Andere Medikamente: Benazapril 29mg daily
Allergien: None
Vorherige Impfungen: Flu shot approximately 8 years ago. Made me sick for three weeks. Dr. Insisted it wasn?t the vaccine but that I was just sick.

VAERS 1785046

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CO
Alter: 39,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 07.10.2021
Beginn: 08.10.2021
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 Balance disorder Chills Dizziness Fatigue Feeding disorder Headache Hyperacusis Hyperhidrosis Hypoaesthesia Injection site pain Injection site vesicles Joint range of motion decreased Migraine Mobility decreased Muscle spasms Myalgia

Symptomtext

10/7/21 ? received shot at 2:45 pm. Other than unconformable at injection site no issues. 10/8/21 1am woke up very thirsty and drank about 8 glasses of water in 30 minutes until thirst was quenched. Went back to bed and the headaches and muscle cramps and joint pain started. Extreme pain causing inability to get comfortable or sleep. Throat started getting tight also. No issues breathing or eating and drinking, just uncomfortable tightness in my throat. Assuming thyroids inflamed. By 5am had a mild fever of 100 degrees. Migraine type headache, sensitive to like and sound, extreme muscle and joint pain preventing me from wanting to move. Sitting up or standing caused dizziness and nausea. Very fatigued and week, had to use walls and tables for support when moving around. About 6am sweets and chills went with raised temperature, 100.5. Muscles would randomly spasm and cause pain. Spent the day laying down. Temp went to normal about 12:30pm. Was unable to eat most the day due to dizziness and nausea. Around 6pm dizziness and nausea subsided, and muscle pain was less. Was able to be in a sitting position in the afternoon. Around 10pm headaches subsided. Was able to get some sleep that night with little pain. Throat still tight. 10/9/21 joint pain, tight throat, mild headache, fatigue, mobility issues with left arm, pain at injection site. Around 10am had dizziness and limbs went tingly and numb. Had the shakes and felt very unsteady. Around 12:30pm dizziness and tingly/numb limbs went away. But still had fatigue, joint pain, tight throat, fatigue, and mobility issues with left arm. 10/10/21 joint pain, fatigue, tight throat, mobility issues with left arm, small red blister and pain at injection site. 10/11/21 joint pain, fatigue, tight throat, mobility issues with left arm, small red blister and pain at injection site. 10/12/21 joint pain, fatigue, tight throat, mobility issues with left arm, small red blister and pain at injection site. 10/13/21 fatigue, tight throat, small red blister at injection site. 10/14/21 fatigue, tight throat, small red blister at injection site. Received single Dose Janssen intermuscular lot#211A21A 10/7/21 2:45pm. Did not contact or seek any treatment. Assumed since no breathing issues not much anyone can do.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Le-Vel Thrive daily supplement vitamins
Allergien: none
Vorherige Impfungen: -

VAERS 1783196

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 30,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Disorientation Erythema Fatigue Feeling abnormal Hypersomnia Hypoaesthesia Pain Piloerection Pyrexia Tremor Vision blurred Vomiting

Symptomtext

Janssen COVID-19 Vaccine EUA 2:00am - severe vomiting that lasted for 6 hours and a fever 5:00am - fever 101.2 and severe body aches 6:00 fever 102 that wouldn't break for 24 hours My body ached so badly, it felt like someone was cutting me open with razor blades, my fever went from 101-102 for 24 hours and would not break, vomiting for 6 hours - I couldn't keep any food or liquids down, my pelvis to toes were completely numb - I couldn't feel my legs at all for 24 hours, my vision was very blurry w/ extreme disorientation for 48 hours, extreme fatigue - I slept for 72 hours (awake maybe 5 of those hours), extreme chills, and body shakes for 48 hours. Big goosebumps all over my body and very red cheeks/forehead for 24 hours. Some of these symptoms lasted about a week after the vaccine (fatigue, soreness and brain fog)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Claritin, zinc, vitamin c & d, echinacea
Allergien: sulfa, cephalosporin, Augmentin, neo/polymyxin, hydrocodone, narcotics, ibuprofen, codeine, Naprosyn, Flomax, contrast iodine, eggs, gluten, shellfish
Vorherige Impfungen: -

VAERS 1782779

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: AZ
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 / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hyperhidrosis Nausea Paraesthesia Peripheral swelling Pyrexia Tremor

Symptomtext

Several hours after receiving the vaccination, I experienced violent shaking/trembling as well as swelling of my limbs and tingling in lower extremities. Other symptoms included fever, sweats and nausea. Symptoms have not resolved completely at time of submission.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: N/A
Allergien: None
Vorherige Impfungen: -

VAERS 1779224

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 52,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 05.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Headache Heart rate decreased Hypotension Nausea

Symptomtext

10/06/2021 dizziness, nauseous, low blood pressure, low pulse, headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Kidney disease, asthma.
Vorgeschichte: Kidney disease, asthma.
Andere Medikamente: Multi vitamin, blood pressure medication, inhaler for asthma.
Allergien: Morphine, bees, hydrocodone.
Vorherige Impfungen: -

VAERS 1777575

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: FL
Alter: 31,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 27.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Chills Fatigue Hypoaesthesia Impaired work ability Injection site pain Paraesthesia Pruritus Pyrexia

Symptomtext

I got my vaccine on 9/27/2021 around 5 pm in order to keep my job, which I started several months ago. The first night I felt mostly fine apart from soreness in my right arm where I was injected. I woke up the next day and felt like a truck hit me - exhausted, weak, fever/chills and tingly skin. I stayed home from work to rest and take care. Later that day the soreness in my upper right arm subsided and my hands felt very itchy, notably between my right thumb, index and middle fingers. I tried to avoid itching. I went back to work on Wednesday the 29th and felt mostly better apart from my arm still itching. Over the course of the next week the itching turned into a tingling/numb sensation that travelled from my fingers into my hand. As I write this now at the keyboard, my entire right arm is tingling and numb. Using my right hand for extended periods of time is a challenge. I am a healthy, 31 year old, active person with a plant-based diet and very health conscious. I'm worried these side effects have not gone away. I do not have a doctor yet and am awaiting health insurance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: I do not have a general practitioner and am awaiting health insurance benefits as I started my job three months ago. I plan to call the health site who provided the injection to see if they have any advice and consult a doctor ASAP.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Men's Health Multivitamin for vegan diet
Allergien: None
Vorherige Impfungen: -

VAERS 1777137

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: OR
Alter: 44,0
Geschlecht: F
Eingang: 11.10.2021
Impfdatum: 28.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Computerised tomogram normal Hypoaesthesia Paraesthesia Urticaria Vision blurred

Symptomtext

Hives, then numbness started in right middle and ring finger then moved up to arm and shoulder. then stared in toes. Toes don't have the tingly feeling like the arm. Now noticing right eye vision is not as good A little blurry.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Went on 9/30/2021 had a CT scan to check for clots. They didn't find anything. Told her to follow up with PCP.
Aktuelle Erkrankungen: No
Vorgeschichte: Hypothyroidism Stage III Kidney Failure
Andere Medikamente: Levothyroxine,
Allergien: PCN, Amoxicillin, salsa, codeine, Has reactions to other vaccinations - hives
Vorherige Impfungen: Hives

VAERS 1775460

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: FL
Alter: 59,0
Geschlecht: M
Eingang: 10.10.2021
Impfdatum: 24.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Paraesthesia Pruritus

Symptomtext

Severe, chronic skin itch with numbing and and tingling throughout both arms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: auto-immune conditions controlled by diet
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1775353

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 09.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anger Autoimmune encephalopathy Condition aggravated Dizziness Feeling abnormal Mast cell activation syndrome

Symptomtext

Autoimmune encephalitis flare. Rage, brain fog, dizzy. GI Mast Cell reaction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Autoimmune Encephalitis, Mast Cell Activation Disorder
Andere Medikamente: Amitryptaline, Synthroid, Advil
Allergien: Penicillin, Demerol, Zofran, Yellowjacket and bee stings
Vorherige Impfungen: -

VAERS 1768714

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: -
Alter: -
Geschlecht: U
Eingang: 07.10.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Gait disturbance Joint swelling Mobility decreased Pain in extremity Paraesthesia

Symptomtext

I was grocery shopping and noticed my foot started tingling. While I was walking to put my groceries in the car, my foot started throbbing with pain and I was barely able to put the cart away. By the time I drove home 5 -10 minutes I could barely walk on it. I laid on the couch and noticed I had chills. My husband brought me an icepack for my foot. We noticed swelling by the ankle near the veins. It felt like a blood clot. I tried to get up but it was so painful, I couldn't put any pressure or weight on it. I had to crawl to the bathroom. I laid in bed for about 4 to 5 hours and noticed the pain was lessening. So I got up and realized I was able to put some weight on it. By morning, I don't have any pain or symptoms. My foot is fine. I'm able to exercise and walk without any symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1765712

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 47,0
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: unbekannt Erholt: nein

Chest discomfort Dyspnoea Headache Hypoaesthesia Mobility decreased Pain in extremity

Symptomtext

Next day sore arm and numb. Unable to lift arm above head. Shortness of breath. Tightness in chest. Headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None and unknown vaccination history
Vorgeschichte: None, but family history of several
Andere Medikamente: -
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1761850

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 59,0
Geschlecht: M
Eingang: 05.10.2021
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: ja

Blood pressure increased Condition aggravated Tinnitus

Symptomtext

Patient was sitting in Post vaccination clinic and asked if we could take his blood pressure because He has tinnitus and the ringing in his ear is a bit louder. Patient reports his normal blood pressure is 135/85. RN took blood pressure 142/86, HR 72, rr 18. Pt reports he had a banana for breakfast. Pt stated he was okay and just wanted to go back to work. Signed understanding that he should call his doctor or go to the ER if symptoms get worse. Left at approximately 10:55

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Tinnitus
Andere Medikamente: None reported
Allergien: NKA
Vorherige Impfungen: -

VAERS 1761434

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: NE
Alter: 48,0
Geschlecht: M
Eingang: 05.10.2021
Impfdatum: 20.09.2021
Beginn: 21.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest pain Diarrhoea Fatigue Headache Heart rate increased Impaired work ability Injection site pain Insomnia Laboratory test Nausea Oral herpes Pain

Symptomtext

Injection site soreness (first 72 hours); Severe Headache (within first 12 hours), caused a day of missed work; Body aches, extreme fatigue (starting about 72 hours after vaccine and continues to Present (Oct 5th)); Cold Sore (appeared 1 week after vaccine); Nausea (appeared 8 days after vaccine); Extreme body aches, fatigue, nausea, diarhea (ramp up at 9 days after vaccine); Missed work days 9-11 after vaccine. Rapid heart rate (appears 10 days after vaccine.); Visited ER on day 12. No sleep/insomnia (nights 10 and 11 after vaccine).; Chest pain (appears day 11 after vaccine); Visited ER on day 12.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Emergency Room tested for blood clots, heart attack, pulminary embolism. They provided IV fluids and a shot of Ativan to try to calm my heart rate. They then sent me home.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1760671

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 35,0
Geschlecht: M
Eingang: 05.10.2021
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Agitation Immediate post-injection reaction Injection site pain Malaise Neck pain Pain Pain in extremity Paraesthesia Screaming Stress Tension Ulna fracture

Symptomtext

Patient was extremely tense on arrival at clinic and curt during all interactions with us. We proceeded with vaccination and immediately upon withdrawal of the vaccine syringe needle from the patient's left deltoid the patient stood up and began yelling and cursing while slamming the wall with his fist(s?) and forearm(s?), with elbow raised at sternal or neck-height and fist above, while exclaiming that his arm hurt badly and we had "hit something" in his arm. Due to scene safety concerns we asked him to follow us out of the clinic, and we walked out of the clinic with him. Once outside of the clinic he seemed to feel unwell and stood leaning forward, we tried to help him sit down, and he later sat with his back leaned against the wall outside. Patient was alert, PWD, nothing seemed obviously medically-abnormal aside from his reported arm pain and level of stress and agitation, vitals not attempted due to scene safety concerns. We offered him a water, which he refused. When asked for more information while again seated, the patient elaborated that upon vaccination he'd felt an instant shooting pain in his left arm, which within less than one second had radiated up the left posterior side of his neck, and he further stated that he had a tingling sensation in his left hand only (we think he slammed that hand into the wall, with a closed fist and ulna and ulnar styloid process experiencing most of the force from impacting the wall). We were unable to inspect the hands of the patient for injury signs due to safety concerns. The patient stated he had violent impulses he was suppressing. When asked if he had previously experienced pain like this from an injection, he stated he had never experienced something like this before. We inspected his arm and it appeared that the vaccination was done in the proper area of his left deltoid, and no band-aid had been applied due scene safety concerns after the vaccine had been injected. We offered him an ice-pack for the area, which he refused. The patient stood up, and the patient stated and/or gestured that it hurt to raise his left arm. We instructed him to try moving it and raising it more as that generally helps, and after a few attempts he seemed to be able to raise it more. He remained alert and dexterous enough to use his smartphone to take a photo of his vaccine card. He stated his arm still hurt. The patient then chose to leave. He left our view, and we think we heard him striking something as he departed, possibly the wall, but we could not see which part of his body, if any, struck something, nor which sort of object may have been impacted, nor what sort of injury pattern could have resulted from those actions. He then apparently walked out of the area of the clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown, further information was not disclosed to us.
Vorgeschichte: Unknown, further information was not disclosed to us.
Andere Medikamente: Unknown, further information was not disclosed to us.
Allergien: Possible allergic history or sensitivity, further information was not disclosed to us.
Vorherige Impfungen: -

VAERS 1760011

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 57,0
Geschlecht: F
Eingang: 04.10.2021
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: ja Erholt: nein

Blood pressure increased Chest X-ray Chest pain Dyspnoea Electrocardiogram Hypersensitivity Laboratory test Oropharyngeal pain Throat tightness

Symptomtext

Over 4 hours, gradual tightness in throat followed by pain at base of throat and pain in center, upper chest. Asymmetric, high blood pressure in left and right arms over an hour. (220/? on right; 180/? on left) Throat tightness subsided but pain remained at base of throat and pain increased in center of chest and was followed by tightness of breath within 24 hours. Pain in chest and shortness of breath was identical to symptoms I experienced for 4 or 5 months following contracting COVID-19 in March, 2020. No fever. No signs of allergic reaction. Pain and shortness of breath lasted over 72 hours and began to improve in the 24 hours following that. Approx. 5 days of symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, chest xray, lab work, oxygen levels, signs of allergic reaction, blood pressure - all normal.
Aktuelle Erkrankungen: none
Vorgeschichte: Hashimoto's Disease, hypertension, arthritis, psoriasis, endometriosis, MS
Andere Medikamente: L-thyroxine, Liothyronine, Naltrexone, Fluoxetine, Deplin, Trazodone, Glatiramer, Meloxicam, Amlodipine, Lisinopril, vit D, multivitamin, fish oil, probiotic, Zyflamend Whole Body (supplement)
Allergien: sulfa, aspirin, Flexoril
Vorherige Impfungen: -

VAERS 1757232

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

moderat

Staat: WA
Alter: 32,0
Geschlecht: F
Eingang: 03.10.2021
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: unbekannt Erholt: ja

Chills Decreased appetite Diarrhoea Dizziness Fatigue Headache Injection site pain Myalgia Nausea Pain Palpitations Pyrexia

Symptomtext

Janssen COVID-19 Vaccine EUA. Starting around 8pm after receiving the vaccine about 5 pm, I started getting severe chills. The chills were causing vigorous full body shivers. My body temp began to rise and I maintained a fever of over 101 degrees until after 1pm the following day. All through the night I had diarrhea, nausea, a headache, and dizzyness with a racing heart rate when I tried to stand. I had muscle aches through the night, particularly in my calves and soles of my feet. After taking 800mg of ibuprofen, my fever dropped below 100 degrees and my body aches subsided until about 6 pm day after injection, then fever began to rise again, chills and nausea returned. So I took another 800 mg ibuprofen before returning to bed and going back to sleep. Major symptoms were gone by the second morning after injection with some lingering fatigue, loss of appetite, and mild body aches. Injection site in arm is also still tender and sore.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Prenatal vitamin, vitamin D3 supplements
Allergien: -
Vorherige Impfungen: -

VAERS 1757054

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: 34,0
Geschlecht: M
Eingang: 02.10.2021
Impfdatum: 26.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anxiety Condition aggravated Constipation Dysuria Headache Nasopharyngitis Nausea Pyrexia Respiratory tract congestion

Symptomtext

103.4 fever x2d, nausea x3d, headache x2d, constipation x3d, difficulty urinating x3d, increased anxiety x4d Congestion/cold 5 days after vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety
Andere Medikamente: Melatonin, wellbutrin
Allergien: None
Vorherige Impfungen: -

VAERS 1756813

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CO
Alter: 69,0
Geschlecht: F
Eingang: 02.10.2021
Impfdatum: 30.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthma Chest discomfort Condition aggravated Pruritus Rash Respiratory rate increased Urticaria

Symptomtext

Fast breathing/lack of air within 1 hr; total body itching after 3 hours; hives/rash on face snd head (used pseudoephedrine and albuterol inhaler - asthma lessened but chest still tight - day 2 still itching all over and tight bronchus but not asthma attack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None - all allergy tests since childhood and history of past reactions to chemicals, meds, allergens - emailed Dr as treated self for asthma attack - if albuterol and pseudoephedrine didn't work, planned on going to urgent care - still itching like crazy on 2nd fat following vaccine.
Aktuelle Erkrankungen: RA, MS - had taken prednisone July-Aug - started Xeljanz Aug.
Vorgeschichte: Asthma, RA, MS, amyloiditis (keep epi pen, albuterol and pseudoephedrine with me at all times. Asthma since infancy so know how to treat emergency attack.)
Andere Medikamente: Well Butrin - had been on Xeljanz but stopped for vaccine, multi vitamins, turmeric & cilantro tea.
Allergien: PEG, formaldehyde, shellfish, certain opioids, tetracyclines, juniper, ragweed, cats, dogs, dust mites, milk intolerant, sulfites/sulfates, nitrates/nitrites, certain food additives.
Vorherige Impfungen: Years ago after flu shot.

VAERS 1753900

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 32,0
Geschlecht: F
Eingang: 01.10.2021
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

Dyspnoea Headache Myalgia Pyrexia

Symptomtext

Fever over 102 F - Tylenol brings it down to 100 F Generalized muscle pain Difficulty breathing Severe headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Atopic dermatitis
Andere Medikamente: -
Allergien: Food allergies (rash) Pollen allergies (difficulty breathing, conjunctivitis, rhinitis)
Vorherige Impfungen: -

VAERS 1745972

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: -
Geschlecht: U
Eingang: 01.10.2021
Impfdatum: -
Beginn: 25.09.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain Abdominal pain upper Adverse drug reaction Angina pectoris Chest pain Dysstasia Headache Heart rate irregular Hypoaesthesia Peripheral swelling Swelling face Vertigo Vision blurred

Symptomtext

FACIAL SWELLING; LEG SWELLING; SEVERE VERTIGO; IRREGULAR HEART RHYTHM; CHEST PAIN; STOMACH PAIN; SEVERE ABDOMINAL PAIN; BLURRED VISION; COULDN'T STAND ON FEET; NUMBNESS IN LEFT SHOULDER/NUMBNESS BEHIND NECK/COULDN'T FEEL THE RIGHT HALF OF HEAD; SEVERE AND PERSISTENT HEADACHE; SHARP AND STEADY HEART PAIN; GENERAL NORMAL SIDE EFFECTS; This spontaneous report received from a patient of unspecified age, sex, race and ethnicity. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no allergies to medication or food at the time of vaccination. The patient had taken no medication or supplements before, at the time or after vaccination. The patient had no other illnesses at the time of vaccination. The patient had no chronic or long-standing health condition at the time of vaccination. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: UNKNOWN) dose was not reported, 1 total administered on 25-SEP-2021:13:35 for prophylactic vaccination. No concomitant medications were reported. On 25-SEP-2021 after receiving the vaccination, patient experienced general normal side effects for two days. On 27-SEP-2021 at 08:00 AM, the patient started to have severe reaction including facial swelling, leg swelling, severe vertigo, irregular heart rhythm problem with sharp and steady heart pain, severe and persistent headache, chest pain, stomach pain, severe abdominal pain, blurred vision, numbness in left shoulder, numbness behind neck and she couldn't feel the right half of her head, and also the patient couldn't stand on her feet. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from general normal side effects on 27-SEP-2021, and the outcome of facial swelling, leg swelling, severe vertigo, irregular heart rhythm, sharp and steady heart pain, numbness in left shoulder/numbness behind neck/couldn't feel the right half of head, severe and persistent headache, chest pain, stomach pain, severe abdominal pain, blurred vision and couldn't stand on feet was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: 20210958258-covid-19 vaccine ad26.cov2.s - sharp and steady heart pain. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no allergies to medication or food at the time of vaccination. The patient had taken no medication or supplements before, at the time or after vaccination. The patient had no other illnesses at the time of vaccination. The patient had no chronic or long-standing health condition at the time of vaccination.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1745972

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: -
Geschlecht: U
Eingang: 01.10.2021
Impfdatum: -
Beginn: 25.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain Abdominal pain upper Adverse drug reaction Angina pectoris Chest pain Dysstasia Headache Heart rate irregular Hypoaesthesia Peripheral swelling Swelling face Vertigo Vision blurred

Symptomtext

FACIAL SWELLING; LEG SWELLING; SEVERE VERTIGO; IRREGULAR HEART RHYTHM; CHEST PAIN; STOMACH PAIN; SEVERE ABDOMINAL PAIN; BLURRED VISION; COULDN'T STAND ON FEET; NUMBNESS IN LEFT SHOULDER/NUMBNESS BEHIND NECK/COULDN'T FEEL THE RIGHT HALF OF HEAD; SEVERE AND PERSISTENT HEADACHE; SHARP AND STEADY HEART PAIN; GENERAL NORMAL SIDE EFFECTS; This spontaneous report received from a patient of unspecified age, sex, race and ethnicity. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no allergies to medication or food at the time of vaccination. The patient had taken no medication or supplements before, at the time or after vaccination. The patient had no other illnesses at the time of vaccination. The patient had no chronic or long-standing health condition at the time of vaccination. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: UNKNOWN) dose was not reported, 1 total administered on 25-SEP-2021:13:35 for prophylactic vaccination. No concomitant medications were reported. On 25-SEP-2021 after receiving the vaccination, patient experienced general normal side effects for two days. On 27-SEP-2021 at 08:00 AM, the patient started to have severe reaction including facial swelling, leg swelling, severe vertigo, irregular heart rhythm problem with sharp and steady heart pain, severe and persistent headache, chest pain, stomach pain, severe abdominal pain, blurred vision, numbness in left shoulder, numbness behind neck and she couldn't feel the right half of her head, and also the patient couldn't stand on her feet. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from general normal side effects on 27-SEP-2021, and the outcome of facial swelling, leg swelling, severe vertigo, irregular heart rhythm, sharp and steady heart pain, numbness in left shoulder/numbness behind neck/couldn't feel the right half of head, severe and persistent headache, chest pain, stomach pain, severe abdominal pain, blurred vision and couldn't stand on feet was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: 20210958258-covid-19 vaccine ad26.cov2.s - sharp and steady heart pain. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no allergies to medication or food at the time of vaccination. The patient had taken no medication or supplements before, at the time or after vaccination. The patient had no other illnesses at the time of vaccination. The patient had no chronic or long-standing health condition at the time of vaccination.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1737805

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 48,0
Geschlecht: F
Eingang: 01.10.2021
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: ja

Anxiety Hypertension Pruritus Respiratory rate increased Tachycardia Fatigue Pain Pain in extremity Pyrexia Urticaria

Symptomtext

15 minutes after vaccination patient became hypertensive, tachy, RR increased and she felt "itchy". 50mg PO benadryl was administered and patient was put in a supine position. After 1 hour her vitals normalized and itchy feeling subsided. Provider assessing attributed event to anxiety.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Indicated "weakened immune system" on screening form
Andere Medikamente: Unknown
Allergien: Yes, unknown to what
Vorherige Impfungen: Moderna. Her PCP recommended she receive Janssen instead and provided patient with a note.

VAERS 1750092

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: OH
Alter: 42,0
Geschlecht: M
Eingang: 30.09.2021
Impfdatum: 30.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Chest pain Dizziness Dyspnoea Headache Pain

Symptomtext

Dizziness and weakness, Shortness of breath, chest pain, and mild headache. The dizziness started around 2:00 pm on September 30th and around 3 PM the same day the weakness, shortness of breath, chest pains, and mild headache started. I did take Acetaminophen at 3:30 PM for pain and the headache started to go away a little around 4 PM. The other symptoms are still present. I have called my primary care physician and am waiting on her response back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Blue rubber bleb nevus syndrome (BRBNS) also known as BEAN syndrome which is a rare congenital vascular anomaly in which malformed veins, or blebs, appear on the skin and surfaces of internal organs. At the time of diagnosis, there were only 200 documented cases worldwide.
Andere Medikamente: Olemsartan Medoxomil 40mg, Flueoxetine HCL 40mg
Allergien: None
Vorherige Impfungen: -

VAERS 1735149

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 30.09.2021
Impfdatum: 22.09.2021
Beginn: 23.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain Chills Dehydration Diarrhoea Fatigue Headache Influenza like illness Menstruation irregular Nausea Pain Vomiting Menstrual disorder Pyrexia

Symptomtext

Flu like symptoms, headache, nausea, fatigue, dehydration, fever, chills. Start of menstrual cycle out of normal expected cycle.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1745129

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: TX
Alter: 63,0
Geschlecht: F
Eingang: 29.09.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Headache Hypertension Nausea

Symptomtext

11:41 am, patient states that she is nauseas and lightheaded. Patient is A/OX3. Vitals : BP 178/119, HR 66, Spo2 98%, RR 20. Patient states that she has a headache. Patient given ice pack and water. BP retaken manually 162/74. Patient states she has no double vision , radial pulses are strong, no tingling or numbness in arms. 11: 50 patient is given orange. 11:55 patient nauseas is relieved. 12:04 vitals retaken : BP 176/78, HR 56, Spo2 96%, RR 18. 12;08 pm patient is advised to go to Hospital or Emergency Room because of her high Blood pressure. Patient states that she is ok and does not need medical attention. RN educates on the importance of going to the ER if high blood pressure persists, if patient experiences chest pain, SOB, visual disturbance. Patient understands and verbalized to seek medical assistance at nearest ER if symptoms worsen at home .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Thyroid Medication ( Patient does not know the name )
Allergien: Morphine, Codeine, Latex
Vorherige Impfungen: Inflammation on vaccinated arm

VAERS 1742386

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: NC
Alter: 35,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 28.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anxiety Dyspnoea

Symptomtext

PATIENT COMPLAINED OF DIFFICULTY BREATHING 10 MINUTES AFTER VACCINE. PUT PULSE OXIMETER ON PATIENT - OXYGEN WAS AT 99. PATIENT SAID THEY ARE HAVING ANXIETY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: OXYGEN WAS AT 99
Aktuelle Erkrankungen: N/A
Vorgeschichte: -
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1741711

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: WA
Alter: 46,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 18.09.2021
Beginn: 20.09.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Electrocardiogram abnormal Laboratory test normal Migraine Pyrexia Ventricular extrasystoles Vomiting

Symptomtext

Migraine, vomit, fever, premature ventricle contractions

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Labs show normal so far, Ekg shows pvc every so often
Aktuelle Erkrankungen: I had a cold about a month before
Vorgeschichte: Muscle inflammation in shoulders, back
Andere Medikamente: Vitamin d, vitamin b, fish oil, ncl, milk thistle
Allergien: Coconut, sulpha drugs
Vorherige Impfungen: -

VAERS 1741701

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CO
Alter: 31,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 28.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Dizziness Dyspnoea Hypopnoea

Symptomtext

1300-Janssen vaccination 0.5ml administered into left deltoid. Patient ambulated to monitoring section of vaccination clinic. 1304- Patient reported complaints of shortness of breath and stated that she has a history of asthma. On assessment patient's skin color was normal for patient, rapid shallow breathing at approximately 36 bpm, patient was AOx4 and was able to independently slow her breathing down with instruction, patient's lung sounds were CTA BL.Patient reported that she had her Albuterol MDI in her car, EMT sent to patient's car to retrieve MDI. Initial vital signs were SaO2 98% RA, HR 119, RR 36. 1307- Patient attempted to administer MDI to herself, patient was observed covering the mouth piece of the MDI and therefore was not able to inhale the medication. At that time this RN administered 3 puffs of MDI while patient closed her mouth over the mouth piece and inhale deeply. Patient remained AOx4 and continued to follow instruction to slow her breathing down. Vitals signs BP 178/96 HR 127, RR 32, SaO2 98%. Lungs CTA BL. 911 was called. 1311- Patient was given 50mg diphenhydramine PO. Patient was able to swallow PO medication without difficulty. Patient had complaints of dizziness. Patient was assisted from a chair to the prone position on the ground. 1317: EMS arrived. Report provided to EMS provider, questions answered, understanding verbalized. Patient ambulated independently to EMS stretcher and was able to independently position herself onto the stretcher. 1320- Patient transported to ER via ambulance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Patient denies acute illness.
Vorgeschichte: Asthma
Andere Medikamente: Albuterol as needed, last dose 9/27/2021. Patient denies using any other medications,, supplements or herbal remedies.
Allergien: Eggs, miralax, oxycodone
Vorherige Impfungen: -

VAERS 1738273

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

moderat

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 27.09.2021
Impfdatum: 27.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest discomfort Chest pain Dyspnoea Pain

Symptomtext

client was sitting in observation room when PHN noticed client holding left upper chest with right hand approximately at 1432. Client stated she was "feeling pain." EMT set up anti-gravity chair and client was able to transfer without assistance. PHN began assessment as EMT began taking vitals. Client was alert and oriented x4, able to answer in full sentences. Client described chest pain as "pressure" as client pointed to upper left chest by collarbone. PHN asked if pain radiated anywhere else and client denied. Client denied shortness of breath, dizziness, blurry vision, or headache. Per client has history of hypertension, diabetes and unspecified thyroid. Client stated she forgot to take blood pressure medication today. Vitals at 1632: oxygen sat 97%, pulse 85, unable to get blood pressure reading. Retake blood pressure at 1635: 160/98. At 1635 client reported feeling "she could not take deep breaths." PHN informed paramedics would be called for further assessment and client declined. At 1636 client stated, "it is all gone." PHN informed client of importance to be further assessed and of her high blood pressure. PHN advised client to stay longer in observation as she only completed her 15 minutes. Client stated she wanted to leave and began standing up. Per client "she would call 911 if she felt the pain again." EMT unable to take anther set of vitals. PHN gave brief education of following up with provider and ER precautions. Per client came with daughter and daughter would drive her home. Client left facility with steady gait at 1639.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, diabetes, unspecified thyroid
Andere Medikamente: unknown names, one for blood pressure
Allergien: -
Vorherige Impfungen: -

VAERS 1736061

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: CO
Alter: 58,0
Geschlecht: F
Eingang: 26.09.2021
Impfdatum: 21.09.2021
Beginn: 21.09.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Headache Impaired work ability Muscle disorder Muscle spasms Tendon disorder Tremor

Symptomtext

Severe, debilitating headache. I never get them. Severe muscle, tendon pulling, cramping throughout body. Weakness. Right hand tremor. Symptoms lasted 3 days. Headache continues although diminished in severity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: I stayed home from work for 3 days.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Nka
Vorherige Impfungen: Flu

VAERS 1723267

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: KY
Alter: 46,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 17.09.2021
Beginn: 17.09.2021
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Feeling of body temperature change Headache Influenza like illness Joint range of motion decreased Joint stiffness Pain Pyrexia Tremor

Symptomtext

At approximately 5:30 pm I began to feel feverish and achy (flu-like symptoms) and by 8:30 pm I was experiencing uncontrollable tremors, severe joint pain throughout my body, intense headache, I couldn?t get warm yet my skin registered a temp of 103.5 with a temporal scan thermometer and felt like it was on fire (the temperature on my forehead never went above 99.1, but scanning other parts of my body produced a reading over 103), and I had lost the ability to open or close my hands. My husband suggested taking me to the hospital, but at the time I was hoping to go to bed and sleep it off. He checked me every 20 minutes to ensure my breathing was normal and if that had weakened or I began experiencing difficulty breathing he would have taken me to the Emergency Room. My breathing remained normal through the entire night. By the next morning, the symptoms remained, but the severity had greatly diminished. I would classify the symptoms at that time more like a flu infection, which was manageable. I had regained the ability to use my hands although the joints in my fingers were stiff and sore. Each day my condition has improved, so I did not seek medical attention.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Bullous Pemphigoid
Andere Medikamente: Unsure
Allergien: -
Vorherige Impfungen: -

VAERS 1722153

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: -
Beginn: 17.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Body temperature Headache Hypokinesia Limb discomfort Pain Pyrexia Tremor

Symptomtext

UNCONTROLLABLE TREMORS; LOST ABILITY TO OPEN OR CLOSE HAND; ACHY(FLU-LIKE SYMPTOMS); SEVERE JOINT PAIN THROUGHOUT THE BODY; MINOR HEAVINESS IN THE ARM; FEVERISH; INTENSE HEADACHE; This spontaneous report received from a patient concerned a female of unspecified age. The patient's height, and weight were not reported. The patient's concurrent conditions included: bullous pemphigoid. The patient was previously treated with influenza vaccine for prophylactic vaccination. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 17-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On 17-SEP-2021, the patient experienced uncontrollable tremors. On 17-SEP-2021, the patient experienced lost ability to open or close hand. On 17-SEP-2021, the patient experienced achy (flu-like symptoms). On 17-SEP-2021, the patient experienced severe joint pain throughout the body. On 17-SEP-2021, the patient experienced minor heaviness in the arm. On 17-SEP-2021, the patient experienced feverish. On 17-SEP-2021, the patient experienced intense headache. Laboratory data included: Body temperature (NR: not provided) 103.5, 99.1. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from minor heaviness in the arm, feverish, achy(flu-like symptoms), uncontrollable tremors, severe joint pain throughout the body, intense headache, and lost ability to open or close hand. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20210917; Test Name: Body temperature; Result Unstructured Data: 99.1; Test Date: 20210917; Test Name: Body temperature; Result Unstructured Data: 103.5
Aktuelle Erkrankungen: Bullous pemphigoid
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1717860

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

moderat

Staat: IN
Alter: 44,0
Geschlecht: F
Eingang: 21.09.2021
Impfdatum: -
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anxiety Burning sensation Dyspnoea Feeling abnormal Paraesthesia

Symptomtext

SHORTNESS OF BREATH; BURNING SENSATION IN BOTH ARMS AND LEGS; TINGLING IN BOTH ARMS AND LEGS; FOGGY FEELING; ANXIETY; This spontaneous report received from a patient concerned a 44 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: UNKNOWN) dose was not reported, administered on 07-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On SEP-2021, the patient experienced anxiety. On 08-SEP-2021, the patient experienced foggy feeling. On 13-SEP-2021, the patient experienced shortness of breath. On 13-SEP-2021, the patient experienced burning sensation in both arms and legs. On 13-SEP-2021, the patient experienced tingling in both arms and legs. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from foggy feeling, had not recovered from tingling in both arms and legs, and the outcome of shortness of breath, burning sensation in both arms and legs and anxiety was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no known allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2664331

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: IN
Alter: 35,0
Geschlecht: M
Eingang: 01.08.2023
Impfdatum: 23.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site reaction

Symptomtext

CHIP IN HIS ARM/SPOT ON HIS ARM THAT WAS HARD AND PROTRUDING ON HIS DELTOID MUSCLE; This spontaneous report received from a patient via a company representative concerned a 35 year old male. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered on 23-SEP-2021 for covid-19 prophylaxis. Age at time of vaccination 35 years old. No concomitant medications were reported. On 30-SEP-2021, the patient experienced chip in his arm/spot on his arm that was hard and protruding on his deltoid muscle. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of chip in his arm / spot on his arm that was hard and protruding on his deltoid muscle was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2597706

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 73,0
Geschlecht: F
Eingang: 16.03.2023
Impfdatum: 11.11.2021
Beginn: 01.10.2022
Tage bis Beginn: 324,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Autoimmune disorder Biopsy skin abnormal Rash macular Rash papular Rash pruritic Rash vesicular Scab

Symptomtext

Little red blistery spots appeared in October 2022. Some itched and some didn't. Some scabbed and some didn't. The first treatment was clobetasol liquid. The second treatment was clobetasol ointment. I saw the doctor and was diagnosed as a lichen rash. After the CEREVE treatment didn't work I was prescribed another treatment. Recently I saw my pulmonologist and told me it is not a lichen rash. When it's all over like this it is condition related to an autoimmune disorder.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash macular
Hospital-Tage: -
Labordaten: Biopsy of skin, abnormal, 01/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Lisinopril; turmeric; melatonin; estradiol; METAMUCIL; multivitamin; acetaminophen; calcium; vitamin D; vitamin B; probiotic; coQ10; BENADRYL
Allergien: Aspirin; temazepam; celery; walnuts; brazil nuts; strawberries; shellfish; rhubarb
Vorherige Impfungen: Hepatitis, I passed out each time, 1990

VAERS 2528775

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OH
Alter: 53,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 08.12.2021
Beginn: 18.08.2022
Tage bis Beginn: 253,0
Dosis: 2
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Exposure to SARS-CoV-2 Pyrexia SARS-CoV-2 test positive

Symptomtext

I started having a cough and low-grade fever that slowly became a high-grade fever and the cough continued. My husband tested positive the day before, so I decided to test once I got the low-grade fever. The test came back positive immediately, I contacted my doctor through the web portal, she prescribed PAXLOVID that I started immediately. The cough continued so the doctor prescribed two rounds of steroids to help me get rid of it. I am now feeling much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Home COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: SYNTHROID; PREVACID
Allergien: No
Vorherige Impfungen: -

VAERS 2497104

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: -
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Off label use Pain assessment Pain in extremity

Symptomtext

OFF LABEL DOSING FREQUENCY; ARM WAS SORE; This spontaneous report received from a patient concerned a female of unspecified age. The patient's weight, height, and medical history were not reported. The patient previously received first dose of covid-19 vaccine ad26. cov2. s (Dose number in series 1) (suspension for injection, route of admin was not reported, batch number: 1805018, expiry: unknown) dose was not reported, 1 total, administered on 06-MAR-2021 for covid-19 prophylaxis. On an unspecified date in 2021, the patient experienced arm was sore with covid-19 vaccine ad26. cov2. s (Dose number in series 1). The patient recovered from arm was sore on 2021. The patient received booster dose of covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: unknown) dose was not reported, 1 total, administered on 06-OCT-2021 for covid-19 prophylaxis which was off label dosing frequency (Dose number in series 2). The product was associated with off label use. No concomitant medications were reported. On an unspecified date in 2021, the patient experienced arm was sore for a couple of days, not long (Dose number in series 2). Patient had no redness or swelling. Laboratory data included: Pain scale 5/10 pain score. At the time of reporting, patient stated that the pain was fully gone. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from arm was sore on 2021, and the outcome of off label dosing frequency was not reported. This report was non-serious. This case, involving the same patient is linked to 20221059775.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain assessment
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: PAIN SCALE; Result Unstructured Data: 5/10 pain score
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2429336

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: UT
Alter: 50,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Insomnia

Symptomtext

3 hours after the vaccination I developed the worst headache I had ever experienced thus far in my life. This headache began to decrease in its intensity after one day and gradually got better until after 2 weeks it was gone. Since the vaccination, I find it much harder to sleep, and as a result of my inability to sleep, I have painful headaches every few months that last weeks at a time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: multivitamin
Allergien: penicillin allergy
Vorherige Impfungen: -

VAERS 2401179

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 04.08.2022
Impfdatum: 11.03.2021
Beginn: 11.04.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Coagulopathy Ear pain Headache Menstrual disorder Myalgia Neuralgia Pain

Symptomtext

Headaches/ear pain/body aches/joint and nerve pain/muscle ache/menstrual disruption/clotting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: HSV-1
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2266788

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: IN
Alter: 55,0
Geschlecht: M
Eingang: 07.05.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature Cough Diarrhoea Headache Illness Pyrexia SARS-CoV-2 test

Symptomtext

SICK 4 TO 5 TIMES SINCE RECEIVING THE JNJ VACCINE; COUGH; DIARRHEA; HEADACHE; LOW GRADE FEVER; This spontaneous report received from a patient concerned a 55 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 26-OCT-2021 for prophylactic vaccination. Age at time of vaccination 55 years old. No concomitant medications were reported. On 05-MAY-2022, Laboratory data included: COVID-19 virus test (NR: not provided) negative. On an unspecified date, the patient experienced sick 4 to 5 times since receiving the JNJ vaccine, cough, diarrhea, headache, and low grade fever. Laboratory data (dates unspecified) included: Body temperature (NR: not provided) Low grade fever (Low grade fever). Treatment medications (dates unspecified) included: ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from headache, and had not recovered from sick 4 to 5 times since receiving the JNJ vaccine, cough, diarrhea, and low grade fever. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Test Date: 20220505; Test Name: COVID-19 virus test; Result Unstructured Data: negative; Test Name: Body temperature; Result Unstructured Data: Low grade fever; Comments: Low grade fever
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2263027

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 35,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 30.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Fatigue Heart rate increased Injection site pain Menstrual disorder Muscle spasms

Symptomtext

Fatigue- 72+ hours Injection sight soreness - 7 days Chills- 16+ hours Elevated heart rate - 95-110 bpm 12+hours starting around 9pm (normal sleep 65-68bpm) Late menstral cycle - 3 days late for first 2 cycles, change in bleeding for all cycles since vaccination (7 cycles), harsh cramps at end/day after period ends,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None yet
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2261747

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: MN
Alter: 77,0
Geschlecht: M
Eingang: 03.05.2022
Impfdatum: 15.05.2021
Beginn: 02.05.2022
Tage bis Beginn: 352,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asymptomatic COVID-19 Diarrhoea Faeces discoloured SARS-CoV-2 test positive

Symptomtext

3 days ago with onset of other symptoms he had multiple episodes of dark diarrhea incidentally COVID positive, denies associated symptoms. Janssen vaccine 5/15/2021 lot number unknown. given at facility

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1889914

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: 57,0
Geschlecht: M
Eingang: 15.04.2022
Impfdatum: 18.09.2021
Beginn: 19.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Cold sweat Fatigue Headache Hyperhidrosis Myalgia Pain Myositis Nausea Pyrexia

Symptomtext

Several hours after the injection the patient woke with fever over 100 degrees, cold sweats, headache, nausea, muscle aches, and body aches. This lasted over 48 hours after which he continued to have severe fatigue and body aches. These symptoms continued until October 14 when he received his first ozone treatment. After the second ozone treatment on 10/21/21 the symptoms resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: none.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1889914

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: 57,0
Geschlecht: M
Eingang: 15.04.2022
Impfdatum: 18.09.2021
Beginn: 19.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Cold sweat Fatigue Headache Hyperhidrosis Myalgia Pain Myositis Nausea Pyrexia

Symptomtext

Several hours after the injection the patient woke with fever over 100 degrees, cold sweats, headache, nausea, muscle aches, and body aches. This lasted over 48 hours after which he continued to have severe fatigue and body aches. These symptoms continued until October 14 when he received his first ozone treatment. After the second ozone treatment on 10/21/21 the symptoms resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: none.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2213402

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 54,0
Geschlecht: M
Eingang: 03.04.2022
Impfdatum: 02.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Tinnitus

Symptomtext

Continued left arm shoulder muscle soreness. Continued tinnitus in both ears but loud and unbearable in left ear especially.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid positive.
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2182265

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: 42,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Headache Nausea Pain

Symptomtext

Severe pain throughout entire body the first night, especially in the brain. I am not sure I would have survived had I not taken the THC gummies preemptively. Extreme nausea the next day, but I had to work anyway.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: brain aneurysm
Andere Medikamente: THC gummies
Allergien: codeine, compazine, dilaudid, fentanyl, latex, mangoes, beets
Vorherige Impfungen: -

VAERS 2174795

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: IN
Alter: -
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Oropharyngeal pain Pain Respiratory tract congestion

Symptomtext

CHEST CONGESTION; SORE THROAT; BODY ACHES; HEADACHE; This spontaneous report received from a patient concerned a 42 year old female. The patient's height, and weight were not reported. The patient's past medical history included: covid-19. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: UNKNOWN) dose was not reported, administered on 26-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced chest congestion, sore throat, body aches, and headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from headache, chest congestion, sore throat, and body aches. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (90 days before the vaccine)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2173161

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 08.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills SARS-CoV-2 test Suspected COVID-19 Throat irritation Vaccination failure

Symptomtext

SCRATCHY THROAT; LITTLE CHILLS; SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 59 year old female of unspecified ethnicity. Initial information was processed along with the additional information received on 07-MAR-2022. The patient's height, and weight were not reported. The patient's past medical history included: In 2019, the patient got covid-19, received an antibody infusion in JAN-2020 and had no other illness at that time, and concurrent conditions included: high blood pressure, alcohol user, non-smoker, and sciatic nerve. The patient had no known allergies. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series: 1) (suspension for injection, route of admin was not reported, batch number: 1808980, expiry: 18-SEP-2021) dose was not reported, 1 total administered on 09-APR-2021 to left arm for prophylactic vaccination. On an unspecified date, following vaccination with covid-19 vaccine ad26.cov2.s, the patient experienced scratchy throat and had tested positive in a PCR (polymerase chain reaction) test which indicated suspected covid-19 infection (mild), and suspected clinical vaccination failure (dose number in series: 1). On 08-DEC-2021, the patient received covid-19 vaccine ad26.cov2.s (dose number in series: 2) (suspension for injection, route of admin not reported, batch number: 211A21A expiry: UNKNOWN) dose was not reported, 1 total administered to left arm for prophylactic vaccination. Concomitant medications included paracetamol (Tylenol) and other anti-inflammatory drugs for sciatic nerve. On 31-DEC-2021, few weeks after receiving the booster vaccination, the patient had taken a covid-19 virus home rapid test which was positive, and had scratchy throat which indicated suspected covid-19 infection, and suspected clinical vaccination failure (dose number in series: 2). The patient's entire family had tested positive. On 02-MAR-2022, the patient was exposed to a peer who had tested positive for covid-19 and the patient experienced scratchy throat, and little chills (dose number in series: 2). The patient had not taken a test for covid-19. The patient stated that she had covid-19 three times so far. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the suspected covid-19 infection, suspected clinical vaccination failure, scratchy throat and little chills was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint: 90000220543. This case, involving the same patient is linked to 20220314408 (dose number in series: 1).; Sender's Comments: V0: 20220312273- COVID-19 VACCINE AD26.COV2.S- Suspected clinical vaccination failure. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211231; Test Name: COVID-19 rapid POC test; Result Unstructured Data: positive; Test Name: COVID-19 PCR test; Result Unstructured Data: positive
Aktuelle Erkrankungen: Alcohol use; Blood pressure high; Non-smoker; Sciatica (Taking Tylenol and other anti-inflammatory)
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (received antibody infusion); Comments: The patient had no known allergies.
Andere Medikamente: TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 1957736

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: KY
Alter: -
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Feeling abnormal Hot flush Nervousness Pain Platelet count Platelet count decreased Thrombocytopenia

Symptomtext

Patient stated that her platelets dropped after she received Covid Vaccine.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Other Case identifier(s): NVSC2021US051773. A 65-year-old female patient received bnt162b2 (BNT162B2) (Batch/Lot number: unknown) as dose number unknown, single for covid-19 immunization. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PLATELET COUNT DECREASED (non-serious), outcome "unknown", described as "Patient stated that her platelets dropped after she received Covid Vaccine.". Relevant laboratory tests and procedures are available in the appropriate section. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: Platelets; Result Unstructured Data: Test Result:Platelets dropped
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2114150

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 32,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 04.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Constipation Diarrhoea Intermenstrual bleeding Irritable bowel syndrome Menstrual disorder

Symptomtext

One week after receiving vaccine, patient began having "IBS" like symptoms with alternating constipation and diarrhea that has not resolved. Patient has also had abnormal periods. Her period ended 5 days before the vaccine and then returned 1 week after the vaccine. since receiving the vaccine she has had spotting for several days between periods.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2092902

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: GA
Alter: 21,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 07.02.2022
Beginn: 07.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Dizziness Hyperhidrosis Pallor Vision blurred

Symptomtext

I administered the vaccine. We were talking. The patient became quiet. I asked if he was ok, he said he felt light headed. He said his vision was blurry. I took his blood pressure - it was 160/157 and he broke a sweat, his coloring paled. I called for my tech to call 911, pulled out my epi pen, & hit go on my bp machine again. This time it read 75/42. I administered epi pen and liquid po benadryl 25mg. His blood pressure began to normalize and his coloring began to return to normal. Bp came back to not crazy 150/85. EMS came - he went with them to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: none yet
Aktuelle Erkrankungen: none known
Vorgeschichte: none known
Andere Medikamente: Today the patient had eaten a protein shake. He also had a nicotine pouch an hour or two before the vaccination.
Allergien: dust mites
Vorherige Impfungen: -

VAERS 2074153

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: GA
Alter: -
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest discomfort Headache Pain Respiratory tract congestion

Symptomtext

BODYACHES; CONGESTION; HEAVY CHEST; HEADACHE; This spontaneous report received from a patient concerned a 39 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: UNKNOWN) dose was not reported, administered on 15-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced bodyaches, congestion, heavy chest, and headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the headache, bodyaches, congestion and heavy chest was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2062059

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: FL
Alter: -
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: -
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Dizziness Fatigue Headache Joint swelling Muscle spasms Pain SARS-CoV-2 test Suspected COVID-19 Vaccination failure

Symptomtext

SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; PAIN; CRAMPING; DIZZINESS; SWELLING JOINTS; WEAKNESS; EXTREME FATIGUE; HEADACHES; This spontaneous report received from a patient concerned a male of unspecified age, race and ethnic origin. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: UNKNOWN) dose was not reported, 1 total administered on 31-AUG-2021 on left arm for prophylactic vaccination. No concomitant medications were reported. On 01-SEP-2021, the patient experienced pain, cramping, swelling joints, extreme fatigue, and headaches that went away four days after, and patient also experienced dizziness, weakness and fatigue that lasted for about a month. On 25-DEC-2021, the patient experienced headaches, cough, itchy throat and weakness (suspected clinical vaccination failure, and suspected covid-19 infection). On 20-JAN-2022, the patient tested positive (twice) for a covid-19 using an antigen rapid test (BinaxNOW). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from pain, cramping, swelling joints, and headaches on 05-SEP-2021, and dizziness, weakness, and extreme fatigue, had not recovered from suspected covid-19 infection, and the outcome of suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000213333.; Sender's Comments: V0: 20220139800-COVID-19 VACCINE AD26.COV2.S-Suspected clinical Vaccination failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Date: 20220120; Test Name: COVID-19 antigen test; Result Unstructured Data: Positive; Test Date: 20220120; Test Name: COVID-19 antigen test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2050104

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: GA
Alter: 42,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: -
Beginn: 17.01.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Oropharyngeal pain

Symptomtext

SORE THROAT; COUGH; This spontaneous report received from a patient concerned a 42 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: UNKNOWN) dose was not reported, administered on 16-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On 17-JAN-2022, the patient experienced sore throat, and cough. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from sore throat, and cough. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no known allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2043294

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WI
Alter: 54,0
Geschlecht: F
Eingang: 18.01.2022
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: ja

Abdominal distension Chills Erythema Fatigue Headache Myalgia Pain Pruritus

Symptomtext

On day 2 I developed an immune response which included, headache, chills, fatigue, myalgias. In addition to that the entire deltoid area was red, itchy, and swollen with intermittent pain that radiated to the wrist and lasted through the week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Sinus
Andere Medikamente: Effexor and Allegra
Allergien: Doxycycline, bee stings, Cephalexine
Vorherige Impfungen: -

VAERS 2037512

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: PA
Alter: 31,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: -
Beginn: 06.01.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Body temperature Feeling hot Pyrexia SARS-CoV-2 test

Symptomtext

FEELING HOT; FEVER; This spontaneous report received from a patient concerned a 31 year old male. The patient's weight was 130 pounds and height was 64 centimeters. The patient's concurrent conditions included: non smoker, and non alcohol user, and other pre-existing medical conditions included: The patient had no known allergies and no history of drug abuse or illicit drug use. The patient was previously vaccinated with covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: unknown and expiry: Unknown) (dose number in series 1), 01 in total was administered on APR-2021, dose was not reported for prophylactic vaccination. No adverse events were reported following administration of covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient additionally received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A and expiry: Unknown) dose was not reported, (dose number in series 2), 01 in total was administered on 11-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 06-JAN-2022, following administration of covid-19 vaccine ad26.cov2.s, he said that felt hot and thought that his fever could be probably due to sudden weather change. On the same day, the patient self-medicated with two Motrin and 1 Motrin the next day. On 06-JAN-2022, he tested his body temperature which was 100.1 degree celsius (C), and has tested twice for (COVID-19) corona virus disease via self test and the result was negative for both tests. On 07-JAN-2022, he again tested his body temperature which was in range of 98-99 degree celsius (C). He used oral thermometer and had been measuring his temperature regularly. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from feeling hot, and fever on 06-JAN-2022 (Dose number in series 2). This report was non-serious. This case was a duplicate of 20220112244.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Test Date: 20220106; Test Name: Body temperature; Result Unstructured Data: 100.1 C; Test Date: 20220106; Test Name: COVID-19 virus test; Result Unstructured Data: negative; Comments: The patient has tested twice for COVID via self test and result was negative for both tests.; Test Date: 20220107; Test Name: Body temperature; Result Unstructured Data: 98-99 C
Aktuelle Erkrankungen: Abstains from alcohol; Non-smoker
Vorgeschichte: Comments: The patient had no known allergies and no history of drug abuse or illicit drug use.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2034097

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: -
Geschlecht: M
Eingang: 14.01.2022
Impfdatum: 03.11.2021
Beginn: 06.01.2022
Tage bis Beginn: 64,0
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

SUSPECTED VACCINATION FAILURE; COVID-19 INFECTION; PAIN IN KNEES; This spontaneous report received from a patient concerned a male of unspecified age. The patient's height and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26. cov2. s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 204A21A expiry: Unknown) dose was not reported, frequency one total, administered left arm on 07-MAY-2021 for prophylactic vaccination. It was unknown if the patient had any adverse event with (dose number in series 1). The patient received booster of covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: unknown) dose was not reported, frequency one total, administered left arm on 03-NOV-2021 for prophylactic vaccination (Dose number in series 2). No concomitant medications were reported. On 06-JAN-2022, the patient experienced diarrhea, sore throat, headaches, muscle pain, pain in legs and knees. Laboratory data included: COVID-19 antigen test (NR: not provided) positive (coded as covid-19 infection and suspected vaccination failure). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from pain in knees and covid-19 infection and the outcome of suspected vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint:90000211250; Sender's Comments: V0:20220112320-COVID-19 VACCINE AD26.COV2.S-Suspected clinical vaccination failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 20220106; Test Name: COVID-19 antigen test; Result Unstructured Data: positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2025939

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: MN
Alter: 59,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 28.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Eczema Erythema Erythema of eyelid Eye swelling Ocular hyperaemia Pruritus Skin exfoliation Skin weeping

Symptomtext

Two days after receiving the vaccine I woke up and my right eye was almost swollen shut, and my eyelid was very red. Eczema rashes in various spots on my face began appearing on my face for the next two weeks; temples, chin, forehead, cheeks. I made an appointment with the dermatologist and was prescribed a steroid gel to apply, and had to discontinue after 30 days, as per dermatologist suggestion. The eczema faded and calmed down a bit in some areas, but then came back with a vengeance on 12/26/21. I woke up and my left eye was almost swollen shut, eye ball was very bloodshot, eye lid bright red, and another spot on my chin and forehead. My face continued to get red, itchy and flaky in almost every area of my face. I am still experiencing redness and flaky patches, with bumps and oozing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Adult Acne
Andere Medikamente: Spironolactone - prescribed for adult acne (taken orally for 11 months prior to vaccine) Retinoid cream - prescribed for adult acne (applied to face for 11 months prior to vaccine) Supplements: Zinc, multi-vitamin, Vitamin C Prebiotic
Allergien: After a two weeks of applying the Retinoid cream, I had a localized flare up of eczema on my face. A steroid cream was prescribed by dermatologist to calm down, which worked.
Vorherige Impfungen: -

VAERS 2020928

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

mild

Staat: -
Alter: 56,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Ear discomfort Ear pain Eustachian tube dysfunction Nasal congestion Respiratory tract congestion Sinus pain Tinnitus

Symptomtext

Within 4 hours of receiving the J&J vaccine I was experiencing tinnitus, nasal congestion, pain in my right ear and sinuses, and a "full" feeling in my right ear. Went to a doctor after about 10 days and was given a 10 days of prednisone and antibiotic for my symptoms and estuation tube dysfunction, After about a month, I was not having the sinus pain and ear pain as much. Still get a "full" feeling and congestion regularly. But the tinnitus has not stopped from it starting.!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1998051

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 08.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Arthralgia Hypoaesthesia Joint stiffness Pain in extremity

Symptomtext

Numbness in left foot. Initially in left ankle and toes as well, now just toes. Occasional sharp pain in left ankle and in arch of foot. Toes have been constantly numb for almost 3 months, there have been no times without numbness. The pain comes and goes. Pain and stiffness in both knees developed in November and continue with some days better than others.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Numbness in left foot. Initially in left ankle and toes as well, now just toes. Occasional sharp pain in left ankle and in arch of foot. Toes have been constantly numb for almost 3 months, there have been no times without numbness. The pain comes and goes. Pain in both knees developed in November and the pain and stiffness has existed ever since.
Andere Medikamente: One a day vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1991119

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: ID
Alter: 42,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Arteriogram coronary normal Bundle branch block left Cardiac septal defect Cardiac stress test abnormal Echocardiogram abnormal Ejection fraction decreased Electrocardiogram abnormal Headache Influenza like illness Lethargy Lipids normal Muscle fatigue Myocardial ischaemia Pain Pyrexia Scan myocardial perfusion abnormal Sleep disorder Ventricular hypertrophy

Symptomtext

11/19/21 - 10:30 0.5ml Vaccine IM left deltoid. - 18:00 PT reports noticeable but mild "flu like" symptoms -Self treats with 800mg NSAID 11/20/21 - PT wakes to mild to severe symptoms that persist for the next 48 hours. These include: fever <103F, muscle fatigue, soreness, headache, and lethargic presentation 11/23/21 - PT's symptoms begin to subside to "mild" over the next 24-36 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: 1,0
Labordaten: 12/2/21 ECG - Abnormal. LBBB 12/3/21 ECG - Abnormal LBBB 12/8/21 LIPID panel - Normal 12/13/21 Nuclear Stress Test - Abnormal - Abnormal myocardial perfusion study. o The left ventricular ejection fraction is calculated at 44 percent. o There is a medium moderate reversible defect in the mid anteroseptal segments and apical septum, consistent with myocardial ischemia. o Wall thickening is abnormal. There is hypokinesis of the mid anteroseptum and apical septum. 12/17/21 Echocardiogram - 09:10 AM BP: 116/80 mmHg - motion is consistent with conduction abnormality. Ejection fraction is visually estimated at 50-55%, consistent with low normal systolic function. 12/20/21 Angiogram -Coronary anatomy Dominance: Right Left main: Angiographically normal Left anterior descending: Angiographically normal Diagonal: Angiographically normal Left circumflex: Angiographically normal Obtuse marginal: Angiographically normal Right cornary artery: Angiographically normal Left ventricle Not performed
Aktuelle Erkrankungen: None
Vorgeschichte: No prior history; PT is a pilot. He receives an annual class and flying class medical examinations. He has no prior history of abnormality.
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1980552

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OH
Alter: -
Geschlecht: U
Eingang: 25.12.2021
Impfdatum: -
Beginn: 19.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Back pain Blood pressure measurement Fatigue Headache

Symptomtext

BACK PAIN STEADILY GETTING WORSE; HEADACHE; FATIGUE; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's height, and weight were not reported. The patient's concurrent conditions included: high blood pressure, back pain, latex allergy, nickel allergy, non alcohol user, and non smoker. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, administered on 26-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 19-DEC-2021, the patient experienced back pain steadily getting worse, headache, and fatigue. Laboratory data (dates unspecified) included: Blood pressure (NR: not provided) High. Treatment medications (dates unspecified) included: oxycodone hydrochloride/paracetamol, and ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from back pain steadily getting worse, headache, and fatigue. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: High
Aktuelle Erkrankungen: Abstains from alcohol; Back pain; Blood pressure high; Latex allergy; Nickel sensitivity; Non-smoker
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1980549

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: 59,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: -
Beginn: 21.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Pyrexia Throat irritation Tinnitus

Symptomtext

COUGHING; BUZZ TO THE LEFT EAR; FEVER; SCRATCHY THROAT; This spontaneous report received from a patient concerned a 59 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered on 14-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 21-DEC-2021, the patient experienced scratchy throat. On 22-DEC-2021, the patient experienced coughing, buzz to the left ear, and fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the scratchy throat, coughing, buzz to the left ear and fever was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1954479

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: IN
Alter: -
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: -
Beginn: 15.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Headache Pain

Symptomtext

This spontaneous report received from a patient concerned a female of unspecified age. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine (suspension for injection, route of admin not reported, batch number: 211A21A expiry: UNKNOWN) dose was not reported, administered on 14-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 15-DEC-2021, the patient experienced body aches. On 15-DEC-2021, the patient experienced chills. On 15-DEC-2021, the patient experienced headache. The action taken with covid-19 vaccine was not applicable. The patient had not recovered from headache, chills, and body aches. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1951530

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: 36,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 13.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Pruritus

Symptomtext

Itching all over. Started about 24 hours after vaccine and lasted about 12 hours. Very similar to the reaction I get from vicodin (although the vicodin itching only lasts a couple hours.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Sertraline; Methylphenidate; Lunesta.
Allergien: Sulfa; Penicillin.
Vorherige Impfungen: -

VAERS 1948625

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 02.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Breast pain Burning sensation Herpes zoster Impaired work ability Rash

Symptomtext

About 4-5 days after the shot I woke up with pain on my right breast and a rash, over the next 2 days it was burning and around my right side. I went to the doctor and was diagnosed with shingles, the NP thinks the vaccine brought down my immune system just enough for the shingles to come out. This led to me having to spend $90 on bandages to keep it covered so my 6 month old son did not get chicken pox. I had to be on an antiviral medicine that caused me to lose the hearing in my left ear for 10 days as well as on norco and ibuprofen for the pain. I missed multiple days of work and was in bed a few days due to the pain. lot # may be 211A217

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No
Vorherige Impfungen: -

VAERS 1938383

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: IN
Alter: 39,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: -
Beginn: 07.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Malaise Myalgia Nausea Pyrexia

Symptomtext

FEELING VERY UNWELL; SEVERE HEADACHES; MUSCLE PAIN; NAUSEOUS; EXTREMELY FEVERISH; This spontaneous report received from a patient concerned a 39 year old male. The patient's height, and weight were not reported. The patient's past medical history included: spinal fusion in neck, and concurrent conditions included: cerebral palsy, and other pre-existing medical conditions included: The patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: UNKNOWN) dose was not reported, administered on 07-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 07-DEC-2021, the patient experienced extremely feverish. On 08-DEC-2021, the patient experienced feeling very unwell. On 08-DEC-2021, the patient experienced severe headaches. On 08-DEC-2021, the patient experienced muscle pain. On 08-DEC-2021, the patient experienced nauseous. Treatment medications (dates unspecified) included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from extremely feverish on 08-DEC-2021, and had not recovered from severe headaches, muscle pain, nauseous, and feeling very unwell. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cerebral palsy
Vorgeschichte: Medical History/Concurrent Conditions: Spinal fusion surgery; Comments: The patient had no known allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1846091

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: PA
Alter: 42,0
Geschlecht: U
Eingang: 07.12.2021
Impfdatum: -
Beginn: 04.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Headache Injection site pain Musculoskeletal stiffness Pyrexia Fatigue Joint stiffness Myalgia

Symptomtext

STIFFNESS; JOINT PAIN; MAJOR HEADACHE; LOW GRADE FEVER; MUSCLE SORENESS AT INJECTION SITE; This spontaneous report received from a patient concerned a 42 year old of unspecified sex. The patient's height, and weight were not reported. The patient's past medical history included: temporomandibular joint (TMJ) disorder, and concurrent conditions included: premenstrual dysphoric disorder (PMDD), penicillin allergy (PCN),drug allergy (sudafed), and season allergies. The patient received covid-19 vaccine ad26.cov2.s (Dose Number in Series: 1, batch number: 202A21A, expiry: 21-SEP-2021) for prophylactic vaccination in 28-APR-2021 and experienced hair loss that began on 15-MAY-2021 where patient notice a more than normal amount and longer duration of hair loss.(Dose Number in Series: 1) The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, (Dose Number in Series: 2), 1 total administered on 04-NOV-2021 11:45 to left arm for prophylactic vaccination. No concomitant medications were reported. On 04-NOV-2021, after 1 hour, the patient began to experienced muscle soreness at injection site. On 05-NOV-2021, morning, the patient experienced joint pain, stiffness, major headache and low grade fever. (Dose Number in Series: 2) The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the joint pain, stiffness, major headache, low grade fever and muscle soreness at injection site was not reported. This report was non-serious. This case, involving the same patient is linked to 20211127938 (Dose Number in Series: 1).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (SUDAFED); Penicillin allergy; Premenstrual dysphoric disorder; Seasonal allergy
Vorgeschichte: Medical History/Concurrent Conditions: Temporomandibular joint disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1916960

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: PA
Alter: 50,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Diarrhoea Fatigue Headache Injection site pruritus Myalgia

Symptomtext

Day 1-Fatigue; Day 2-Mild symptoms including fatigue, diarrhea, itching at injection site, headache, joint pain, muscle aches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: Turmeric
Allergien: N/a
Vorherige Impfungen: Pain at injection site, fatigue, mild fever; Age 49; Moderna; Covid19; 4/20/2021

VAERS 1913563

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

mild

Staat: SC
Alter: 19,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood pressure decreased Rash

Symptomtext

After receiving Janssen Vaccine patient's BP dropped to 70/42. Patient was laid down in a supine position. BP increased to 98/62 and patient was sat back up. BP continued to remain stable at 110/60. Nurse then noticed a fine rash on limbs and trunk. Benadryl was administered and BP dropped again to 72/56. patient was laid back down in a supine position and BP increased to 118/72. Patient was transported to the hospital via EMS and was given prednisone and discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: NKA
Vorherige Impfungen: -

VAERS 1912214

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: IN
Alter: 20,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: -
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Ageusia Anosmia Chills Cough Headache Pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

COUGH; RUNNY NOSE; BODY ACHE; LOSS OF TASTE; LOSS OF SMELL; CHILLS; HEADACHE; This spontaneous report received from a patient concerned a 20 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient is otherwise healthy and no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: UNKNOWN) dose was not reported, administered on 02-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On NOV-2021, the patient experienced cough. On NOV-2021, the patient experienced runny nose. On NOV-2021, the patient experienced body ache. On NOV-2021, the patient experienced loss of taste. On NOV-2021, the patient experienced loss of smell. On NOV-2021, the patient experienced chills. On NOV-2021, the patient experienced headache. Laboratory data included: COVID-19 virus test positive (NR: not provided) Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from headache, cough, runny nose, chills, body ache, loss of taste, and loss of smell. This report was non-serious. This report was associated with product quality complaint.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 202111; Test Name: COVID-19 virus test positive; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient is otherwise healthy and no known allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1888590

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 54,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Aphonia Arthralgia Blood test C-reactive protein increased Chills Headache Impaired work ability Joint range of motion decreased Joint swelling Joint warmth Lower respiratory tract congestion Metabolic function test normal Musculoskeletal stiffness Oropharyngeal pain Pyrexia Quality of life decreased Red blood cell sedimentation rate increased Respiratory tract congestion

Symptomtext

headache, fever, chills, extreme joint pain, swelling, stiffness, hot to touch, sore throat, chest congestion, weight loss X 2 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Blood work 11-8-21; WBC 16.7, sed rate 62, CRP6.3, CMP WNL
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension, GERD
Andere Medikamente: metoprolol 50mg daily, omeprazole 20mg daily, losartan 100mg daily. vit c, vit d,
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1888590

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 54,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Aphonia Arthralgia Blood test C-reactive protein increased Chills Headache Impaired work ability Joint range of motion decreased Joint swelling Joint warmth Lower respiratory tract congestion Metabolic function test normal Musculoskeletal stiffness Oropharyngeal pain Pyrexia Quality of life decreased Red blood cell sedimentation rate increased Respiratory tract congestion

Symptomtext

headache, fever, chills, extreme joint pain, swelling, stiffness, hot to touch, sore throat, chest congestion, weight loss X 2 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Blood work 11-8-21; WBC 16.7, sed rate 62, CRP6.3, CMP WNL
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension, GERD
Andere Medikamente: metoprolol 50mg daily, omeprazole 20mg daily, losartan 100mg daily. vit c, vit d,
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1893994

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WI
Alter: 35,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Myalgia

Symptomtext

On and off continuous headache and muscle pain between shoulder blade

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fluoxetine
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1893705

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OK
Alter: 44,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Computerised tomogram Headache Magnetic resonance imaging Mucosal hypertrophy Pain in extremity

Symptomtext

Arm soreness and headache within the hour of getting the shot. The arm soreness abated after a day or two, but the headache has continued NON-STOP ever since. OTC headache medicines Tylenol, Naproxen, Aspirin do not make the headache stop. Tramadol 50mg, Toradol 10mg, Topamax 25mg don't even temporarily relieve the headache. Amoxicillin 125Mg has been prescribed to help with any possible immune deficiency.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: CT scan on 10/21/2021 plus a full blood workup to check for potential clotting was inconclusive. Pain not subsiding. MRI on 11/18/2021. No clotting, but showed THICKENING OF THE MUCOSAL LINING. Anti-inflammatory meds have thus far proved ineffective. Went to Chiropractor on 11/22/2021 to see if an adjustment might provide some relief. Thus far, the headache persists.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: SRONYX
Allergien: None
Vorherige Impfungen: -

VAERS 1877708

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

mild

Staat: TN
Alter: 55,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 06.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Arthritis Back pain Muscle rigidity Musculoskeletal stiffness Neck pain

Symptomtext

Pain and rigidity at joints of both hands, shoulders with corresponding inflammation. Pain and stiffness in back and neck.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: multivitamin
Allergien: none
Vorherige Impfungen: -

VAERS 1873798

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: MT
Alter: 52,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 29.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Pruritus Urticaria

Symptomtext

After the vaccine I developed red, itchy welts under my Estradiol patches that never happened previously. I changed my patches every 3.5 days before and after the vaccination as I was supposed to, and every single time after the vaccine I developed a red, itchy welt, that, like I said, never happened prior to the vaccine. They are still there on my torso, but almost gone. The patches I was using were fine until I got the vaccine. I ended up notifying my doctor and she requested to change the patches to the non-generic, but my insurance would not approve. I then had to change to a gel, which is MUCH more expensive than my original patches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None, just a change in medications due to allergic reaction to the one I was on once I received the vaccine.
Aktuelle Erkrankungen: -
Vorgeschichte: Fibromyalgia, arthritis, anxiety disorder, asthma, migraines, sleep apnea, spondylitis, Addies Tonic Pupil, nausea, diarrhea, severe foot pain, dyspnea,
Andere Medikamente: Vitamin B12, Turmeric, Vitamin D3, Opcon A eye drops, diphenhydramine, Lutein, Elderberry, Vitamin A, aspirin, clobetasol topical, progesterone, fluconazole, montelukast, albuterol, clonazzepam, tramadol, acyclovir, testosterone topical, Es
Allergien: Morphine, codeine, many environmental allergies
Vorherige Impfungen: -

VAERS 1873705

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 42,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Dizziness Feeling hot Hypoaesthesia

Symptomtext

Pt stated dizzy asked ambulance to be called. While waiting for ambulance pt continued to experience dizziness and reported feeling hot and numb in left arm. Pt asked if he had eaten and was offered water and lollipops. Paramedics arrived and took pt to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: nkda
Vorherige Impfungen: -

VAERS 1869153

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TN
Alter: 46,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Diarrhoea Feeling cold Hyperhidrosis Nausea Pain Sleep disorder Vomiting

Symptomtext

Woke up from sleep around 1215AM with chills, unable to get warm. Woke up again around 0215 with sweats, nausea, vomiting, body aches and diarrhea. Lasted until approximately 0730 when I took a dose of Phenergan to stem the nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: N/A
Vorgeschichte: Morbid obesity, Migraines, Anxiety, Depression, ADD, seasonal allergies
Andere Medikamente: Celexa 40mf PO daily; Claritin 10mg PO daily; MVI w/ iron daily; Vitamin D3 50mcg daily. Immitrex 100 mg po PRN migraine; Fiuricet 1 tab PO Q4hr PRN migraine; Phenergan 12.5mg PO Q5hr PRN migraine Meloxicam 1 tab PO daily PRN joint pain; ES
Allergien: NKA/NKDA
Vorherige Impfungen: Flu shot - always causes whelp and itching at site

VAERS 1867876

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

mild

Staat: CO
Alter: 35,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 24.09.2021
Beginn: 10.10.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site discolouration Skin discolouration

Symptomtext

Skin discoloration, injection site hypopigmentation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site discolouration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1867668

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OK
Alter: 57,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 30.09.2021
Beginn: 05.10.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Hypoaesthesia Muscular weakness

Symptomtext

Headache to top of left side of head and to left forehead above brow. Increased numbness and weakness of left lower extremity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Psoriatic arthritis, psoriasis, hyperlipidemia, hyperglycemia, arthritis
Vorgeschichte: Hyperlipidemia, hyperglycemia, arthritis
Andere Medikamente: Cyclobenzaprine, Gabapentin, Sulfasalazine, Atorvastatin, Vitamin D3, Vitamin B12, Fish Oil
Allergien: None
Vorherige Impfungen: -

VAERS 1865154

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 69,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 26.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Contusion Erythema Induration Limb mass Pain Rash Ultrasound scan normal

Symptomtext

Less than a week after booster, my leg had bumps that were hard and big. The lumps were on my left leg, the middle of my thigh down to my knee. It felt and looked black, blue, and red. My doctor got me in on Monday 11/08/21. I was taken to get an ultrasound which confirmed it's not a deep vein clot. I was told to use warm compresses and wear compression socks. I was told to take Aleve for pain and that it should be gone in a couple of weeks and if not, I am to go back to the doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Ultrasound- Varicose Vein Clot
Aktuelle Erkrankungen: No
Vorgeschichte: Thyroid condition
Andere Medikamente: Levothyroxine Calcium Magnesium
Allergien: Gluten Intolerance
Vorherige Impfungen: Moderna- Flu 1 day

VAERS 1854693

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CO
Alter: 22,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal discomfort Chills Electrocardiogram Headache Pain in extremity

Symptomtext

Two minuets post vaccination client experienced severe arm pain, severe headache, upset stomach. Client was placed on mat on floor with feet raised and cool cloth applied to forehead. Provided client juice. At 1012 client began to shiver and teeth shattered uncontrollably and continued to complain of right sided head pain. Client denied shortness of breath or difficulty breathing. At 1023 clients symptoms continued with no improvement and EMS was called to evaluate. At 1026 EMS arrived and performed a 12 lead EKG and assessment with no abnormal findings. Client refused transport to hospital. At 1100 client provided snack and symptoms shivering resolved but head pain still 8 out 10. Client called mother who transported client home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: EMS performed assessment and 12 lead EKG.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1851794

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OR
Alter: 63,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 24.09.2021
Beginn: 11.10.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Diarrhoea Faecal elastase test Faeces discoloured Pancreatic failure Stool analysis abnormal

Symptomtext

Developed yellow diarrhea which after a stool sample test has been determined to be Exocrine Pancreatic Insufficiency (EPI)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Fecal Elastase Test 11/1/2021. Results 11/8/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Melanoma
Andere Medikamente: Opdivo
Allergien: None
Vorherige Impfungen: -

VAERS 1848876

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: MT
Alter: 38,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood pressure fluctuation Chills Cough Dysgeusia Nausea Night sweats Pain Pyrexia Vomiting

Symptomtext

Started running a fever 4 hours after injection. Ran a fever of 102 for 10 days. Accompanied by chills, body aches, a cough, and on day 9 and 10 vomiting. Blood pressure was also erratic, and have been monitoring it for a month, Finally stabilizing 5 weeks later. Also, 6 weeks after the shot, still having Nausea and night sweats. Also a metalic taste in my mouth.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Hashimotos
Andere Medikamente: Liothyronine, Levothyroxine
Allergien: Amoxilcillian, Molds, Grasses,
Vorherige Impfungen: Flu

VAERS 1841215

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CO
Alter: 38,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Urticaria

Symptomtext

Broke out in hives

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1840023

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

mild

Staat: TX
Alter: 38,0
Geschlecht: M
Eingang: 03.11.2021
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

Injection site erythema Injection site swelling Pain Pain in extremity Pyrexia

Symptomtext

Sore arm, red, raised bump at injection site, body aches. 103.0 fever for 48 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: Type 1 diabetic
Andere Medikamente: Insulin--Novolin R and N. Lisinopril 10mg
Allergien: Codene and lipitor allergy
Vorherige Impfungen: -

VAERS 1836528

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: FL
Alter: 31,0
Geschlecht: M
Eingang: 02.11.2021
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: nein

Headache Malaise Pain Pyrexia

Symptomtext

He had a fever, body pains, mild headache from last night with malaise. He was given T tylenol 650mg as needed for 48 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Nil just observation
Aktuelle Erkrankungen: nil
Vorgeschichte: Nil
Andere Medikamente: T tylenol 650mg as needed for fever
Allergien: Nil
Vorherige Impfungen: -

VAERS 1836016

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TN
Alter: 35,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 22.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia

Symptomtext

Joint pain in anterior aspect of feet upon waking

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Pre-natal vitamin Magnesium Calcium
Allergien: None
Vorherige Impfungen: -

VAERS 1831671

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: 40,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Dizziness

Symptomtext

Pt started feeling dizzy at 11:57 after receiving the vaccine. Pt stated he did not eat anything before coming in. Pt also stated that something similar happened before in the past. Pt stated having high level of anxiety before being vaccinated. Pt initial vital signs- HR50; O2 98% ; lungs clear HR54; O2 98% bp 120/60 12:29am- bp 140/58;hr 47while standing; 02 98% Pt cleared @12:29

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1831449

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

mild

Staat: ID
Alter: 30,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pyrexia

Symptomtext

Prolonged fever of 102? (4+ hours). Tylenol and ice packs will not bring down

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Dairy
Vorherige Impfungen: -

VAERS 1827191

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OH
Alter: 41,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: -
Beginn: 21.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Muscle twitching Pain in extremity

Symptomtext

SORE ARM; TWITCHING OF ARM/MINOR TWITCHING ALL OVER THE BODY(FEET, LEGS, BACK); This spontaneous report received from a patient concerned a 41 year old female. The patient's weight was 112 pounds, and height was 60.5 inches. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: UNKNOWN) dose was not reported, administered on 20-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On 21-SEP-2021, the patient experienced twitching of arm/minor twitching all over the body (feet, legs, back). On an unspecified date, the patient experienced sore arm. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sore arm, and had not recovered from twitching of arm/minor twitching all over the body(feet, legs, back). This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1825755

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 44,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 05.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Abdominal pain lower Abdominal pain upper Appendicectomy Appendicitis Computerised tomogram abdomen abnormal Laparoscopic surgery Pain

Symptomtext

Pt began having sharp, burning epigastric pain and RLQ pain the night of 10/21 and worsening on 10/22. Pt seen 10/22 at a health care facility for evaluation and referred to a second Hospital ER for further evaluation. CT abd/pelvis "most consistent with mild early acute appendicitis" and pt was admitted to hospital. Pt had laparoscopic appendectomy performed 10/23 by Dr.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain lower
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension, vitamin d deficiency, hyperlipidemia, obstructive sleep apnea, frequency of micturition
Andere Medikamente: amlodipine, multivitamin, cetirizine, turmeric, vitamin b-12, vitamin d-3, voltaren 1% topical gel
Allergien: ioversol, polyethylene glycol
Vorherige Impfungen: -

VAERS 1825273

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: AZ
Alter: 60,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Nausea Parosmia Taste disorder Vomiting

Symptomtext

Projectile Vomit within 8 to 10 hours after the shot. Sense of smell and taste distorted, everything smells and tastes like gasoline and produces more nausea. It has continued for a month now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sensitivity to preservatives, flavor enhancers, stabilizers in fooods
Vorherige Impfungen: -

VAERS 1821664

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 46,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Bone pain Dysgeusia Feeling abnormal Headache Mouth swelling Nausea Pain

Symptomtext

Excruciating bone pain began the evening of the injection. Bone pain to that degree lasted approximately one week, followed by an additional 8 days of bone pain. Bone pain finally resolved on day 17. Use of Tylenol/Ibuprofen did not relieve bone pain. Other symptoms included sporadic stabbing head pain through day 12. Swollen mouth, body aches, nausea, metallic taste in mouth, overall feeling poorly continue to present off and on through today (day 17).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Type 1 diabetes
Andere Medikamente: Novolog, Vitamin B, C and D, zinc, calcium/magensium.
Allergien: Benzodiazepines.
Vorherige Impfungen: -

VAERS 1814766

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

mild

Staat: TX
Alter: 51,0
Geschlecht: M
Eingang: 25.10.2021
Impfdatum: 05.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Computerised tomogram Headache

Symptomtext

Headaches for the past several weeks, possible Bells Palsy. Getting CT scan to rule out brain bleeds

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Waiting results
Aktuelle Erkrankungen: None
Vorgeschichte: Diabeties
Andere Medikamente: ASPIRIN EC 81 MG TABLET LIOTHYRONINE SOD 5 MCG TAB LOSARTAN POTASSIUM 50 MG TAB ROSUVASTATIN CALCIUM 20 MG TAB CARVEDILOL 6.25 MG TABLET NOVOLOG 100 UNIT/ML VIAL LEVOTHYROXINE 150 MCG TABLET
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1813291

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 41,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Muscle spasms Rash

Symptomtext

severe pelvic cramps 1 day after vaccination drug rash 5 days after vaccination on back, arms, chest & leg

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Physical exams
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: sertraline 50mg, vitamin D 5,000 IUs, collagen
Allergien: None
Vorherige Impfungen: -

VAERS 1810187

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: AZ
Alter: 54,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: -
Beginn: 19.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature Chills Decreased appetite Fatigue Injection site pain Malaise Pain Pyrexia

Symptomtext

FEELING VERY SICK; FATIGUE/ FEELING REALLY TIRED; FEVER OF 102F; ARM PAIN AT INJECTION SITE; POOR APPETITE/ NOT AT ALL HUNGRY AND STILL CAN'T EAT THIS MORNING; BODY ACHES; FELT COLD AND HAD CHILLS; This spontaneous report received from a patient concerned a 54 year old female. The patient's weight was 135 pounds, and height was 62 inches. The patient's concurrent conditions included: kidney issue, penicillin allergy, and migraines, and other pre-existing medical conditions included: Patient was not pregnant at the time of report. The patient experienced drug allergy when treated with acetylsalicylic acid, ibuprofen, oxycodone hydrochloride/paracetamol, and acetylsalicylic acid/caffeine/homatropine terephthalate/oxycodone hydrochloride/oxycodone terephthalate/phenacetin for drug used for unknown indication. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered on 19-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 19-OCT-2021, the patient experienced poor appetite/ not at all hungry and still can't eat this morning. On 19-OCT-2021, the patient experienced body aches. On 19-OCT-2021, the patient experienced felt cold and had chills. On 19-OCT-2021, the patient experienced fatigue/ feeling really tired. On 19-OCT-2021, the patient experienced fever of 102F. On 19-OCT-2021, the patient experienced arm pain at injection site. Laboratory data included: Body temperature (NR: not provided) 102 F. On 20-OCT-2021, the patient experienced feeling very sick. Treatment medications included: naproxen sodium. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from felt cold and had chills, and had not recovered from fatigue/ feeling really tired, fever of 102F, arm pain at injection site, body aches, poor appetite/ not at all hungry and still can't eat this morning, and feeling very sick. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211019; Test Name: Body temperature; Result Unstructured Data: 102 F
Aktuelle Erkrankungen: Kidney disorder (patient sees a urologist for kidney issue x20 years.); Migraine; Penicillin allergy
Vorgeschichte: Comments: Patient was not pregnant at the time of report.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1804259

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 04.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anti-ganglioside antibody Asthenia Blood thyroid stimulating hormone C-reactive protein Electrophoresis Feeling abnormal Full blood count Hypoaesthesia Limb discomfort Muscle fatigue Nervousness Quality of life decreased Red blood cell sedimentation rate Vitamin B12

Symptomtext

Symptoms started 3 days after vaccine with bilateral numbness/tingling in hands and fingers. Next day muscle fatigue and weakness spread to both wrists and firearms. And it continued to slowly progress to both arms and legs, gluts, and slightly in the face. Weird sensation off and on feeling. Felt like I just worked out my arms and my legs felt heavy and shaky like I didn?t have my weight under them. Uncomfortable feelings and it has been affecting my quality of life since the symptoms started. The symptoms have stabilized but not improved, and at this point I am at 2 weeks of constant symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Muscle fatigue
Hospital-Tage: -
Labordaten: Lab work on 10/12: vitamin B1, electrophoresis, sed rate, crp, tsh, CBC, ganglioside antibody test. EMG test on 10/18. All lab work and tests came back normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Finasteride 1 mg, vitamin c 500mg, nac 600mg, zinc 22mg, vit d 3000 ius. Took aspririn 81 mg a couple hours after vaccine and the next day.
Allergien: None
Vorherige Impfungen: -

VAERS 1804250

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: PA
Alter: 48,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 07.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Ear pain Headache Lymph node pain Lymphadenopathy Myalgia Pyrexia Rash

Symptomtext

SWELLING/PAIN LYMPHNODE IN ARMPIT OF LEFT ARM AS WELL AS RIGHT EAR; HEADACHE; FEVER; CHILLS; MUSCLE ACHES; RASH ON LEFT CHEEK ON FACE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: PROBIOTIC; ZINC, VITAMIN C, VITAMIN D, MULTIVITAMIN
Allergien: SULFA
Vorherige Impfungen: -

VAERS 1801967

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: AZ
Alter: 56,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 05.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Limb discomfort Pain in extremity Sleep disorder

Symptomtext

Pressure/Pain on both legs starting the night of vaccine injection. Has continued each night, for the past 2 weeks, during sleep hours causing sleep interruption due to uncomfortable feeling. Pressure/Pain has increased in intensity and now is constant throughout the day. Cannot sit for long periods of time due to pressure/pain and uncomfortable feeling in the legs, specifically behind the knee area.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Blood work to assess blood levels and antibody test.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None known.
Vorherige Impfungen: -

VAERS 1801627

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CO
Alter: 23,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Feeling abnormal Pain in extremity Unresponsive to stimuli

Symptomtext

Patient received vaccine. Complained of pain in arm. Went out to car to get water and came back into the clinic, sat down in a chair and became unresponsive. Patient recovered consciousness about 10 seconds later. States he remembers feeling lightheaded and felt a "headrush." Patient remembers waking back up in chair. He was laid down on the floor with feet up and give a cookie and water.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1798252

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: -
Alter: 18,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Asthenia Fatigue Headache Pyrexia White blood cell count decreased

Symptomtext

Last Friday, October 9, my daughter was vaccinated at about 12pm, during the day she reported strong headache episodes, she took paracetamol 750mg, on Saturday she felt tired and weak for the whole day, but at night she felt a little better so she decided to go out a little, she came back home due to a fever, on Sunday, she had high fever, the whole day so in the evening she entered the emergency room they found her white cells very low, so she went straight to clinic, on Wednesday she was discharged but she is still hospitalized we are treating her with antibiotics but she is still has a fever, I would like to know if her condition has any relation with the vaccine, if there are other cases reported and how it is been treated. I am looking forward to hearing from you asap.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 10,0
Labordaten: We have to access the hospital records, I can send over email
Aktuelle Erkrankungen: None
Vorgeschichte: none
Andere Medikamente: Prozac 20mg
Allergien: Dipirona
Vorherige Impfungen: -

VAERS 1797785

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: 50,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 08.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Rash Rash pruritic Urticaria

Symptomtext

Patient received the Jansen Covid-19 Vaccine on 10/08/21 and on 10/09/21 started having a rash and hives appear from head to toe. She reports that the rash was also itchy. She went to a telehealth visit in which she was prescribed a topical steroid cream. She later went to an Urgent Care and received a steroid shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1783782

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 40,0
Geschlecht: M
Eingang: 19.10.2021
Impfdatum: -
Beginn: 13.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature Chills Feeling hot Flushing Headache Interchange of vaccine products Medication error Muscle spasms Nasal congestion Pain

Symptomtext

BODY ACHES; CRAMPING IN LEGS; FEEL HOT; FACIAL FLUSHING; STUFFY NOSE; BAD CHILLS (DREAMING THAT WAS STUCK IN SNOW) / FREEZING AND SHAKING BAD AND UNCONTROLLABLY (FELT LIKE A TRUCK RAN OVER); HEADACHE; POTENTIAL MEDICATION ERROR (ADMINISTRATION OF FIRST DOSE OF MODERNA VACCINE BEFORE JANSSEN VACCINE); This spontaneous report received from a patient concerned a 40 year old male. The patient's height, and weight were not reported. The patient's past medical history included: Clostridioides difficile, muscle eating infection in right arm, left wrist surgery, dialysis, coma, hit by a car, head injury, and shattered knee, and concurrent conditions included: shingles, kidney failure, non alcohol user, smoker, and Charlie horses, and other pre-existing medical conditions included: The patient had history of drug abuse or illicit drug usage (had a substance abuse problem and has been clean for several years). The patient experienced drug allergy when treated with haloperidol for drug used for unknown indication. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose was not reported, administered on 13-OCT-2021 18:00 for prophylactic vaccination. The batch number was not reported and has been requested. Concomitant medications included miRNA 1273 for prophylactic vaccination. On 13-OCT-2021, the patient experienced potential medication error (administration of first dose of Moderna vaccine before Janssen vaccine). On 14-OCT-2021, the patient experienced body aches. On 14-OCT-2021, the patient experienced cramping in legs. On 14-OCT-2021, the patient experienced feel hot. On 14-OCT-2021, the patient experienced facial flushing. On 14-OCT-2021, the patient experienced stuffy nose. On 14-OCT-2021, the patient experienced bad chills (dreaming that was stuck in snow) / freezing and shaking bad and uncontrollably (felt like a truck ran over). On 14-OCT-2021, the patient experienced headache. Laboratory data (dates unspecified) included: Body temperature (NR: not provided) One degree above normal. Treatment medications (dates unspecified) included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from bad chills (dreaming that was stuck in snow) / freezing and shaking bad and uncontrollably (felt like a truck ran over), and cramping in legs, had not recovered from body aches, headache, feel hot, facial flushing, and stuffy nose, and the outcome of potential medication error (administration of first dose of moderna vaccine before janssen vaccine) was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Result Unstructured Data: One degree above normal.
Aktuelle Erkrankungen: Abstains from alcohol; Cramps in legs; Kidney failure (kidney failure was on dialysis.); Shingles (Had shingles about a month ago. Have a tiny bit of a rash and a little bit of itching still remaining); Smoker (Vape trying to quit).
Vorgeschichte: Medical History/Concurrent Conditions: Automobile accident; Coma; Dialysis (kidney failure was on dialysis.); Diarrhea, Clostridioides difficile (Twice); Head injury; Infection; Knee fracture; Wrist surgery; Comments: The patient had history of drug abuse or illicit drug usage (had a substance abuse problem and has been clean for several years).
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1795992

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 18,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Dyskinesia Pain in extremity

Symptomtext

After receiving vaccine pt had Jerky movements for 2 to 4 minutes and then he felt ok. Pt stated that he had some pain in the arm after the shot and felt dizzy and can not remember anything until he felt better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: paramedics were called they tested bp , blood sugar levels etc everything was normal.
Aktuelle Erkrankungen: NO
Vorgeschichte: NO
Andere Medikamente: NO
Allergien: NO
Vorherige Impfungen: -

VAERS 1793573

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: UT
Alter: 56,0
Geschlecht: M
Eingang: 16.10.2021
Impfdatum: 11.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Neck pain Tinnitus Visual impairment Vomiting

Symptomtext

Thursday evening after work , I started to have headaches starting at my lower neck ( brain stem area) getting worse over the next 4 hour to the point of seeing spots, bad pain to the point of vomiting, because of the pain, head throbbing, like zI could feel my pulse pounding in my entire head, ringing in my ears.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None taken
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: I have had reactions in the past to tetanus shot, years ago
Vorherige Impfungen: 25 yrs old tetanus shot, broke out in rash and swelling

VAERS 1790086

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 41,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: -
Beginn: 14.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dysmenorrhoea Fatigue Pain

Symptomtext

SEVERE MENSTRUAL CRAMPING, NO DISCHARGE; DOUBLING OVER IN PAIN; FATIGUE (COULD GO LAY DOWN AND TAKE A NAP); This spontaneous report received from a patient concerned a 41 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: alcohol user, and non smoker, and other pre-existing medical conditions included: The patient had no known allergies. The patient did not have any history of drug abuse or illicit drug use. The patient had finished period last week (Saturday). The patient was taking vitamins in past. The patient was previously treated with sertraline for drug used for unknown indication. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, administered on 13-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-OCT-2021, the patient experienced severe menstrual cramping, no discharge. On 14-OCT-2021, the patient experienced doubling over in pain. On 14-OCT-2021, the patient experienced fatigue (could go lay down and take a nap). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from severe menstrual cramping, no discharge, fatigue (could go lay down and take a nap), and doubling over in pain. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Alcohol use (very minimal. 1 drink per month.); Non-smoker
Vorgeschichte: Comments: The patient had no known allergies. The patient did not have any history of drug abuse or illicit drug use. The patient had finished period last week (Saturday). The patient was taking vitamins in past.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1790061

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: IL
Alter: 42,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: -
Beginn: 08.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Fatigue Gait disturbance Headache Joint swelling Pain Pain in extremity Peripheral swelling Pyrexia

Symptomtext

SWOLLEN ANKLES; SWOLLEN FEET; CHILLS; LEFT ARM PAIN THAT FEELS LIKE IT IS IN THE BONE (FROM THE SHOULDER ALL THE WAY TO THE FINGER TIPS); BODY PAIN (HIPS ALL THE WAY DOWN TO BOTH FEET); TOO PAINFUL TO WALK; FEVER; HEADACHE; FATIGUE; This spontaneous report received from a patient concerned a 42 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, and batch number: 211A21A expiry: UNKNOWN) dose was not reported, administered on 08-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-OCT-2021, the patient experienced fatigue. On 09-OCT-2021, the patient experienced body pain (hips all the way down to both feet). On 09-OCT-2021, the patient experienced too painful to walk. On 09-OCT-2021, the patient experienced chills. On 09-OCT-2021, the patient experienced left arm pain that feels like it is in the bone (from the shoulder all the way to the finger tips). On 09-OCT-2021, the patient experienced fever. On 09-OCT-2021, the patient experienced headache. On 10-OCT-2021, the patient experienced swollen ankles. On 10-OCT-2021, the patient experienced swollen feet. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body pain (hips all the way down to both feet), too painful to walk, chills, fever, and headache on 10-OCT-2021, and swollen ankles, and swollen feet on 11-OCT-2021, and had not recovered from fatigue, and left arm pain that feels like it is in the bone (from the shoulder all the way to the finger tips). This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1789948

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TN
Alter: 60,0
Geschlecht: M
Eingang: 16.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pruritus Urticaria

Symptomtext

Small hives occurred on the left forearm and the forearm started to itch, approximately 6 hours after the shot was administered at 3:10 PM. The itching progressed on the left forearm and started on the right arm over the next 20 to 30 minutes. If you put it on a 1-10 scale, 10 being the worst itch. The left arm was an 8 and the right was a 2. The right arm did not appear to have any noticeable hives. No swelling occurred in the face or throat. When the forearm itching progressed to the point it became unbearable an 8. A topical Cortisone-10 ointment was applied on both forearms and one Clemastine Fumarate 1.34mg tablet was administered. This helped with the forearm itching, it went down to a 1.5. Experienced random itches on the head, neck, back, and legs; 7 to 12 hours after the shot was administered. No hives where present in any other body locations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None at this time.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin C & D daily
Allergien: Aspirin, ASA
Vorherige Impfungen: -

VAERS 1789908

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: -
Beginn: 07.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Burning sensation Head discomfort Headache Pyrexia

Symptomtext

BURNING SENSATION IN FACE AND NECK; HEAD PRESSURE; LOW FEVER; HEADACHE; This spontaneous report received from a patient concerned a 43 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, administered on 07-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 07-OCT-2021, the patient experienced burning sensation in face and neck. On 07-OCT-2021, the patient experienced head pressure. On 07-OCT-2021, the patient experienced low fever. On 07-OCT-2021, the patient experienced headache. Treatment medications (dates unspecified) included: paracetamol, and ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from low fever, and had not recovered from burning sensation in face and neck, head pressure, and headache. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no known allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1785747

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 53,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 28.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Balance disorder Dizziness Oral pain Palatal swelling

Symptomtext

2 days after small bump on roof of mouth. Very tender and painful for 6-7 days. Continued dizzy and balance issues. No injection site soreness but 5 days post injection shoulder joint in injection arm incredibly sore for 6+ days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Dr. visit to review bump on roof of mouth and continued dizziness and balance issues on Oct 1, 2021. Dr. examined and advised to give it a few more days.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 1785432

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: 57,0
Geschlecht: F
Eingang: 14.10.2021
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: nein

Anxiety Fatigue Headache Pain Pyrexia

Symptomtext

Approximately 3 hours after receiving the J & J vaccine I developed a bad headache. I took 2 Ibuprofen but still had a slight headache. On Wednesday, Oct. 13th, I still had a headache and as the day progressed it became more intense. At approximately 6 p.m. I started to feel achy and anxious. About an hour later a severe fever began. My body not only aches but I would rate the amount of pain at around an 8. My husband wanted to take me to the hospital but I did not think I could handle the trip and did not want to call an ambulance knowing that this was more than likely a response to the vaccine. This hell lasted for about 12 hours. I am writing this on the 14th of October. It is 2:00 p.m. and I am still running a slight fever with fatigue and headache. This struggle has been much more difficult than when I had Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1783023

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 26,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Hypoaesthesia Immediate post-injection reaction Injection site hypoaesthesia

Symptomtext

Patient received Janssen COVID vaccine in our facility on 10/4/21. She immediately developed left arm, left jaw, and neck numbness. She was monitored for 30 minutes with BP and pulse oximetry. All reactions resolved during that time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site hypoaesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1779694

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: AZ
Alter: 46,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 05.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Body temperature increased Fatigue Headache Myalgia

Symptomtext

I got a headache, a slight increase in temperature, and fatigue for the first two days. These symptoms subsided, but I have had lingering muscle and joint pain. I got the J&J COVID-19 vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Sleep-apnea and arthritis.
Andere Medikamente: Multi-vitamin and vitamin D
Allergien: Bacterium (medication)
Vorherige Impfungen: I believe I received the anthrax vaccine in the service. I was about 26 years old. I believe I developed arthritis as a result

VAERS 1776669

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 11.10.2021
Impfdatum: 25.09.2021
Beginn: 25.09.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Vomiting

Symptomtext

Vomiting; dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Muscle spasm
Andere Medikamente: Syeda
Allergien: Ofloxacin; Penicillin
Vorherige Impfungen: influenza vaccine causes vomiting

VAERS 1776334

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OK
Alter: 48,0
Geschlecht: M
Eingang: 11.10.2021
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

Arthralgia Pain Pyrexia

Symptomtext

In the hours following injection I became febrile ( T- 101.6) and extremely achy with severe joint pain. Treatment consisted of acetaminophen and rest. Fever lasted for 48 hours. Body aches continued to through the 72 hour mark.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1775877

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: MS
Alter: 34,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Diarrhoea Diarrhoea haemorrhagic Faeces discoloured Pain Pyrexia

Symptomtext

Diarrhea progressing to Black and bloody diarrhea starting within 6h post injection and resolving 48h-72h later. Additionally fevers, chills and body aches were present 12h post injection and lasted for ~24h duration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1773420

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 09.10.2021
Impfdatum: -
Beginn: 03.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Lymphadenopathy Pain in extremity Somnolence Tenderness Throat irritation

Symptomtext

LIKE A GLAND WAS SWOLLEN ON THE FRONT OF NECK, LIKE A BUMP AND IT WAS TENDER TO TOUCH; TENDERNESS IN THROAT; TENDERNESS UNDER CHIN; SLEEP ALL DAY; SORE ARM; SO FATIGUED; This spontaneous report received from a patient concerned a 74 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient experienced drug allergy when treated with macrogol. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A and expiry: 14-DEC-2021) dose was not reported, administered on 01-OCT-2021 15:00 for prophylactic vaccination. No concomitant medications were reported. On 03-OCT-2021, the patient experienced sleep all day. On 03-OCT-2021, the patient experienced sore arm. On 03-OCT-2021, the patient experienced so fatigued. On 04-OCT-2021, the patient experienced tenderness under chin. On 05-OCT-2021, the patient experienced tenderness in throat. Treatment medications included: paracetamol. On 07-OCT-2021, the patient experienced like a gland was swollen on the front of neck, like a bump and it was tender to touch. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sleep all day, sore arm, and so fatigued on 06-OCT-2021, and had not recovered from tenderness under chin, tenderness in throat, and like a gland was swollen on the front of neck, like a bump and it was tender to touch. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1771948

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: NE
Alter: 50,0
Geschlecht: F
Eingang: 08.10.2021
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

Bone pain Chills Fatigue Feeling abnormal Feeling hot Headache Myalgia Pain

Symptomtext

5:30 that evening, foggy, chills, but hot couldn't get warm, full body muscle aches couldn't hardly touch anything everything hurt including my bones had a headache and fully exhausted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone pain
Hospital-Tage: -
Labordaten: haven not gone in just still tired 3 days later
Aktuelle Erkrankungen: Just a lot of sinus infections
Vorgeschichte: Chronic Sinus infection
Andere Medikamente: Musinex, allergy shots, OHM allergy pil, magnesium, Vit E, A, C, B12, E, Zinc
Allergien: Sulfa and Bactrium
Vorherige Impfungen: -

VAERS 1771859

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 50,0
Geschlecht: M
Eingang: 08.10.2021
Impfdatum: 07.10.2021
Beginn: 08.10.2021
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 discomfort Pyrexia

Symptomtext

So far fever (99-102), discomfort in left arm at injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site discomfort
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, type 2. Arthritis in left hip.
Andere Medikamente: Just the Johnson and Johnson vaccine
Allergien: Sulfa, Metformin, Penicillin, Amoxicillin
Vorherige Impfungen: Influenza, 2016

VAERS 1771797

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OH
Alter: 64,0
Geschlecht: F
Eingang: 08.10.2021
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

Periorbital swelling Pruritus Rash Sinus congestion Swelling face

Symptomtext

Pt. states that after receiving the 1st dose of J&J 10/01/2021, started experiencing symptoms 10/06/2021 of itchy face, rash across on the side of the right neck, sinus congestion, and puffy eyes. Self-treating with Benadryl, still continuing to experience symptoms. No noted Primary visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multi-Vitamins
Allergien: Aspirin, Cashews
Vorherige Impfungen: -

VAERS 1768857

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 68,0
Geschlecht: M
Eingang: 07.10.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Hyperhidrosis Injection site swelling Lymph node pain Lymphadenopathy Night sweats Pain Rash

Symptomtext

Full body rash that started within 12 hours of injection and lasted another 36 hours General aches and chills and swelling at site of injection that lasted about 48 hours Painful Lymph node swelling under both arms, but the worst was under the right arm that started about 36 hours after injection and is still very sensitive, but the swelling is decreasing. 3 consecutive nights of night sweats, worst night was soaking bed clothes and sheets

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Monoclonal Gammathoy
Andere Medikamente: None
Allergien: Tetanus
Vorherige Impfungen: Flu and tetanus

VAERS 1765098

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OR
Alter: 49,0
Geschlecht: M
Eingang: 06.10.2021
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Headache Ocular hyperaemia Vasodilatation

Symptomtext

Evening and night after being vaccinated had severe headache and woke up with one eye severely blood shot due to blood vessels opening up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperthyroidism (minor)
Andere Medikamente: Vitamin D Vitamin B-Complex
Allergien: Allergic to gluten Allergic to most pitted fruits
Vorherige Impfungen: -

VAERS 1762041

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge #211A21A

mild

Staat: UT
Alter: 22,0
Geschlecht: F
Eingang: 05.10.2021
Impfdatum: 04.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Chest discomfort Chills Cough Crying Decreased appetite Fatigue Headache Injection site pain Irritability Malaise Pain Parosmia Pollakiuria Pyrexia Sleep disorder

Symptomtext

Unusual and unexpected side effects of the vaccine. About 12 hours after vaccine administration: waking through the night, irritability and crying, overly frequent need to pee (within 30 seconds of fluid intake & at least once every 2 hours) ? along with the more common side effects body aching, weakness, soreness at injection site, and fever. Within 24 hours of receiving the vaccine, also experienced parosmia & ensuing total loss of appetite, severe malaise (urge to shiver, chest discomfort resulting in urge to cough), and the more common side effects fatigue and headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1761326

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 211A21A

mild

Staat: IN
Alter: 40,0
Geschlecht: M
Eingang: 05.10.2021
Impfdatum: 17.09.2021
Beginn: 18.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Disturbance in attention Feeling abnormal Insomnia Joint range of motion decreased Memory impairment

Symptomtext

Severe shoulder pain and loss of motion. Loss of motion 50% for day 1-7 and still painful and 10-20% loss of motion 18 days later. Loss of sleep for the first 2 weeks after the injection. Brain fog has been very bad since the day after the injection. I sometimes forget what I'm doing, can't focus at work, and I find myself struggling while doing a task that takes more than just a few moments. I have to force myself to pay attention and my attention keeps getting pulled away from whatever task I am doing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: I have an appointment with my doctor soon.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1761326

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge 211A21A

mild

Staat: IN
Alter: 40,0
Geschlecht: M
Eingang: 05.10.2021
Impfdatum: 17.09.2021
Beginn: 18.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Disturbance in attention Feeling abnormal Insomnia Joint range of motion decreased Memory impairment

Symptomtext

Severe shoulder pain and loss of motion. Loss of motion 50% for day 1-7 and still painful and 10-20% loss of motion 18 days later. Loss of sleep for the first 2 weeks after the injection. Brain fog has been very bad since the day after the injection. I sometimes forget what I'm doing, can't focus at work, and I find myself struggling while doing a task that takes more than just a few moments. I have to force myself to pay attention and my attention keeps getting pulled away from whatever task I am doing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: I have an appointment with my doctor soon.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1757587

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: LA
Alter: 45,0
Geschlecht: M
Eingang: 03.10.2021
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Back pain Chills Hyperhidrosis Hypoaesthesia Insomnia Nausea Pain in extremity Pollakiuria Pyrexia Rash

Symptomtext

Fever, violent chills, sweating, joint pain, back pain, nausea, arm pain, numbness in left fingers, left shoulder pain, soreness,(left shoulder), sleeplessness, frequent urination with little to no urine, rash (spread across neck collar region, up and down entire spine, and under pectorals).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Psuedochlolineterase Deficiency (Sp?)
Vorherige Impfungen: -

VAERS 1757488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 211A21A

mild

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 03.10.2021
Impfdatum: 03.10.2021
Beginn: 03.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness

Symptomtext

Client completed 15 minutes in the observation area and walked to the EMT station. EMt asked the client if she was feeling good. The client reported that she feels, " a little bit dizzy." RN Withers recommended the client stay in observation due to the dizziness. The client stated she wanted to go sit back in her seat. RN and EMT responded to the client at 1:49PM. The client said she felt, "A little bit lightheaded when I stood up." The client reported a history of low blood pressure. The client has a history of anaphylaxis related to anesthesia. The client reported a history of anxiety. Vitals obtained by EMT at 1:51PM were as follows: automatic BP 114/86, O2 99%, HR 74. The client denied any persistent symptoms. The client stated she has only consumed coffee and a cookie today. The client requested to leave the vaccination site against medical advice. RN provided education regarding s/s of anaphylaxis and when to seek EMS. The client voiced understanding of this education.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Anxiety
Andere Medikamente: Unknown
Allergien: Anesthesia
Vorherige Impfungen: -

VAERS 1757058

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 03.10.2021
Impfdatum: 26.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Headache Nausea

Symptomtext

Headache x2d, nausea x2d

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Idiopathic intermittent rash
Vorgeschichte: Chronic sinusitis
Andere Medikamente: None
Allergien: PCN, rocephin
Vorherige Impfungen: -

VAERS 1732603

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 03.10.2021
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: unbekannt Erholt: nein

Ear discomfort Eye swelling Hypersensitivity Rash Rash papular Erythema Feeling hot Pruritus Rash macular Scratch Rash pruritic Skin exfoliation Skin warm Swelling face Urticaria

Symptomtext

I scheduled a COVID-19 vaccination for 09/24/2021. On 09/24/2021, I got an allergic reaction after ~30 minutes of receiving the Janssen J&J vaccine. Allergic reaction included raised welts/rashes on lower, middle back and both ears were heated and irritated. I was given two Benadryl tablets (antihistamine) and was monitored until the symptoms subsided. I went home and woke up the next day on 09/25/2021 to find there were red itchy rashes on my arms and across my chest and my areola/nipple area. I contacted the nurse and he told me to take an antihistamine. I took Zyrtec and the symptoms subsided. On the third day, 09/26/2021, after the Zyrtec wore off, I found that symptoms came back more severe. My neck and chest was had red large rashes/bumps that were itchy and my ears were irritated and heated. I then took another Zyrtec and it subside after a few hours. I continued to take Zyrtec and contacted my doctor on 09/27/2021. My doctor told me to continue taking Zyrtec for two weeks from the day of the vaccine. However, my symptoms of rashes and heated/warming/ irritated ears came back on and off. On 10/01/2021, I woke up and noticed that my eyes and face was swollen which subsided after I took Zyrtec again. Later, my skin on my eyelids and face was slowly peeling away kind of like after a rash. My symptoms are still persisting. I am not sure what would happen if I stop taking the antihistamine. I plan to see the doctor soon again to see what they can do to help this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Shrimp, some seafood (but not allergic to fish), and nickel allergy.
Vorherige Impfungen: -

VAERS 1732603

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 03.10.2021
Impfdatum: 24.09.2021
Beginn: 24.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Ear discomfort Eye swelling Hypersensitivity Rash Rash papular Erythema Feeling hot Pruritus Rash macular Scratch Rash pruritic Skin exfoliation Skin warm Swelling face Urticaria

Symptomtext

I scheduled a COVID-19 vaccination for 09/24/2021. On 09/24/2021, I got an allergic reaction after ~30 minutes of receiving the Janssen J&J vaccine. Allergic reaction included raised welts/rashes on lower, middle back and both ears were heated and irritated. I was given two Benadryl tablets (antihistamine) and was monitored until the symptoms subsided. I went home and woke up the next day on 09/25/2021 to find there were red itchy rashes on my arms and across my chest and my areola/nipple area. I contacted the nurse and he told me to take an antihistamine. I took Zyrtec and the symptoms subsided. On the third day, 09/26/2021, after the Zyrtec wore off, I found that symptoms came back more severe. My neck and chest was had red large rashes/bumps that were itchy and my ears were irritated and heated. I then took another Zyrtec and it subside after a few hours. I continued to take Zyrtec and contacted my doctor on 09/27/2021. My doctor told me to continue taking Zyrtec for two weeks from the day of the vaccine. However, my symptoms of rashes and heated/warming/ irritated ears came back on and off. On 10/01/2021, I woke up and noticed that my eyes and face was swollen which subsided after I took Zyrtec again. Later, my skin on my eyelids and face was slowly peeling away kind of like after a rash. My symptoms are still persisting. I am not sure what would happen if I stop taking the antihistamine. I plan to see the doctor soon again to see what they can do to help this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Shrimp, some seafood (but not allergic to fish), and nickel allergy.
Vorherige Impfungen: -

VAERS 1756993

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 19,0
Geschlecht: M
Eingang: 02.10.2021
Impfdatum: 02.10.2021
Beginn: 02.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Hyperhidrosis Pallor

Symptomtext

Upon sitting down in observation area, client became pale, diaphoretic, and reported feeling dizzy. Client assisted into cot to lie down. Provided water and granola bars. Advised to report adverse effects to primary care provider and VSAFE. Advised client to call 911 or seek emergency medical services if side-effects worsen or severe side-effects develop. Client observed for 30 minutes and vital signs taken every 5 minutes. Adverse effects completely resolved after 30 minutes and client left site unassisted with steady gait.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Denies
Vorgeschichte: Denies
Andere Medikamente: None
Allergien: Denies
Vorherige Impfungen: -

VAERS 1756836

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

mild

Staat: ID
Alter: 56,0
Geschlecht: F
Eingang: 02.10.2021
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Arthralgia Headache

Symptomtext

It's been 10 days and I still have a headache that won't go away and pain in my joints.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1755746

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 02.10.2021
Impfdatum: -
Beginn: 25.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Fatigue Headache Pain Pyrexia

Symptomtext

SLIGHT HEADACHE AT THE BASE OF THE HEAD (WAS STILL LINGERING BUT VERY MILD), THEN IT GOT WORSE; FEELING TIRED; FEVER; BODY ACHES, (WAS LITTLE BIT SORE); CHILLS; This spontaneous report received from a patient concerned a 48 year old female. The patient's weight was 135 pounds, and height was 64 inches. The patient's concurrent conditions included: fibroids, alcohol consumer, non smoker, and perimenopause, and other pre-existing medical conditions included: The patient had no known allergies, and no any drug abuse/illicit drug usage. Medication for fibroids and perimenopause- vitamins. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, administered on 25-SEP-2021 for prophylactic vaccination. Concomitant medications included progesterone for perimenopause, and fibroids. On 25-SEP-2021, the patient experienced body aches, (was little bit sore). On 25-SEP-2021, the patient experienced chills. On 25-SEP-2021, the patient experienced feeling tired. On 25-SEP-2021, the patient experienced fever. On 26-SEP-2021, the patient experienced slight headache at the base of the head (was still lingering but very mild), then it got worse. Treatment medications (dates unspecified) included: ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body aches, (was little bit sore) on 27-SEP-2021, and fever on 26-SEP-2021, had not recovered from slight headache at the base of the head (was still lingering but very mild), then it got worse, and feeling tired, and the outcome of chills was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Alcoholic (Patient had some red wine last night (on 29-SEP-2021)); Fibroids (Medications- progesterone (bioequivalent) and vitamins); Non-smoker; Perimenopause (Medications- progesterone (bioequivalent) and vitamins)
Vorgeschichte: Comments: The patient had no known allergies, and no any drug abuse/illicit drug usage. Medication for fibroids and perimenopause- vitamins.
Andere Medikamente: PROGESTERONE
Allergien: -
Vorherige Impfungen: -

VAERS 1754950

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 42,0
Geschlecht: M
Eingang: 01.10.2021
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Cough Fatigue Impaired work ability Pain

Symptomtext

Sustained coughing fits. Woke up every 5-25min from approx 2am on. Chills, Whole body soreness, so tired couldn't work at all.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Had cough. Not sure if post viral cough from COVID (I had that just over a month ago) or if due to allergies.
Vorgeschichte: Allergies.
Andere Medikamente: Vit C, D3, Zinc, Vit multi, Albuterol, hayfever herbal remedies
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1754563

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 60,0
Geschlecht: M
Eingang: 01.10.2021
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: nein

Arthralgia Disorientation Dizziness Headache Memory impairment Nausea Pain in extremity Neck pain Pyrexia

Symptomtext

LHS arm pain elbow to lower neck, pain scale 6-7. Dizziness. Mid-grade headache LHS. Severe nausea. DISORIENTATION - Brief/sporatic unfamiliarity with in-home surroundings - initiated 1500 hrs, continuing thru present ... 1730hrs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: coq10, tumeric circummin, D3, C, fish oil, aspirin, multi vitamin
Allergien: hay fever. allergy to Cipro, Penecillin, Clyndamyacin
Vorherige Impfungen: -

VAERS 1753264

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OH
Alter: 35,0
Geschlecht: M
Eingang: 01.10.2021
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

Angina pectoris Dizziness postural Headache Pyrexia

Symptomtext

Started running high fever and headache at about 9:45pm on the date of vaccine 9/29/21 still running a fever today 10/01/21. On. 9/30/21 couldn't get out of bed except to use the bathroom due to headache and fever. 10/01/21 I still have slight headache fever has reduced. However I am dizzy anytime I stand for any amount of time I have started to have pain around my heart area as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness postural
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None known
Vorgeschichte: None known
Andere Medikamente: None
Allergien: None known
Vorherige Impfungen: -

VAERS 1750551

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 30.09.2021
Impfdatum: 23.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Pruritus Rash

Symptomtext

Rash on both feet and lower legs 5 days post shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Contacted for advice. Prescribed hydrocortisone. Did not help the itching
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1750132

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OH
Alter: 25,0
Geschlecht: M
Eingang: 30.09.2021
Impfdatum: 28.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Myalgia Pyrexia

Symptomtext

Patient reports fever of 102 F on 9/29/21 morning. Muscle aches, chills. patient reports he no longer has fever as of 9/30/21. He now reports while his BP is 120/60 and his pulse is 65 , that he feels there is something wrong with his heart. I old him to seek attention at the ER /or urgent care if he needed to. patient was extremely nervous and did not want to get the shot at all but was mandated by work. I suggested to him that perhaps it was anxiety over getting the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1749733

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: MN
Alter: 22,0
Geschlecht: F
Eingang: 30.09.2021
Impfdatum: 27.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Headache Nausea Pyrexia Vomiting

Symptomtext

Chills, fever, vomiting, nausea and headaches. Saw patient on day 3 and still having these symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1749563

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

mild

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 30.09.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Pain Pain in extremity

Symptomtext

Headache, body ache, pain, sore arm all over

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Asthma
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1749534

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: MN
Alter: 61,0
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: unbekannt Erholt: ja

Dizziness Electrocardiogram Vision blurred

Symptomtext

A few minutes after the vaccine administration (0815) patient reported he was having blurred vision, was also feeling light-headed. BP was 79/41, HR in 40's. Supportive care provided to patient, oral fluids given. Patient became less unresponsive, but maintained airway and respirations. Patient was also assisted to lay down. At 09:24, patient became more alert. EMS was called and patient was also evaluated by our MD. He returned to baseline and did not require transportation to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: EKG performed by emergency medical personnel.
Aktuelle Erkrankungen: Right eye pain s/p assault
Vorgeschichte: Anxiety, sleep difficulty, reports temporal lobe seizure history
Andere Medikamente: Vistaril Tylenol Ibuprofen
Allergien: Mayonnaise
Vorherige Impfungen: -

VAERS 1742346

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TN
Alter: 59,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 27.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Feeling cold Headache Myalgia Pain Pruritus Pyrexia Urticaria

Symptomtext

Had few welts after injection. The next morning woke up freezing/temp 101.6/ aches all over / headache/ every muscle hurt Took aleve. At 6 am. Took 2 ASA at 1230 pm. Felt exactly like I felt when I had covid. Continued to have itchy small red areas pop up through out the day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Took 2 aleve at time vaccine
Allergien: None
Vorherige Impfungen: -

VAERS 1741875

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 49,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 25.09.2021
Beginn: 25.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anxiety Chills Dizziness Feeling hot Pallor Panic attack

Symptomtext

After 15 minutes of receiving injection, I had a panic attack. I felt as if I was going to pass out. So Informed the pharmacist she had me put my legs up, wasn?t helping. So i laid on the floor and put my legs on a chair. My body felt extremely hot, my husband said I lost coloring in my face. After about 30 minutes, I was able to get up and walk to my car with assistance. I had chills for 2 days. I am still having issues with anxiety attacks and consulted with my nurse practitioner. We are monitoring at home and if I feel I can?t manage, she will call in a prescription for me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1741802

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 46,0
Geschlecht: M
Eingang: 28.09.2021
Impfdatum: 07.09.2021
Beginn: 07.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dysphagia Headache Pain Respiratory rate increased Symptom recurrence

Symptomtext

One hour after receiving 1st pfizer dose patient started to experience trouble swallowing. Headache then body aches followed shortly after. For about 4 hours client experienced increased breathing then went to bed. Duration of 48 hours for difficulty swallowing, headache, and body aches and they all self resolved (no medications taken). Client did not follow up with primary care physician. Client then experienced throat symptoms of difficulty swallowing after having 1 beer at family party 4 days after pfizer 1st dose vaccination date. Symptoms lasted for about 3 hours and then the client went to bed. The next morning symptoms self resolved. Medical consult was elevated through health care coordinators. Janssen as second dose was recommended by MD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes, Psoriasis
Andere Medikamente: Metformin 500 mg PO BID, Atorvastatin 5 mg PO at bedtime, cortisone topical cream.
Allergien: Seasonal Allergies in spring to pollen
Vorherige Impfungen: -

VAERS 1741567

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 27.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Injection site erythema Injection site swelling Interchange of vaccine products Urticaria

Symptomtext

At approximately 1100, patient reported to Lead Nurse she received a 1st dose of Moderna. Patient received her first dose of Moderna (LOT# 042L20A) on 01/17/2021 in left arm. Patient reported a first dose reaction. One day after her vaccination, patient noted left arm redness and swelling at the injection site. Patient immediately went to urgent care. Urgent care doctor advised patient to go to the emergency room. Patient was hospitalized for one night in the emergency room and reported hives all over the body. Lead nurse elevated to supervisor. Supervisor elevated to medical consult team. Medical consult team advised patient to receive a single dose of Janssen Covid vaccine. At 1342, patient received a single dose of Janssen (LOT# 211A21A, exp. 12/14/2021) in right arm. Patient advised to wait in observation for 30 minutes. Lead Nurse educated patient on signs/symptoms of when to seek emergency care, to follow up with primary care provider, and to sign up on v-safe. At approximately 1412, patient left facility with unlabored respirations and steady gait.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: None reported
Allergien: None reported
Vorherige Impfungen: At age 52, pt received her first dose of Moderna (LOT# 042L20A) on 01/17/2021 in left arm. Patient reported a first dose reacti

VAERS 1741318

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 22.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Feeling abnormal Headache Nausea Pain

Symptomtext

Today is day 6 and I am still having body aches, headache, nausea and brain fog.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: High BP, chronic body pain
Andere Medikamente: Procardia, hydrochlorothiazide, zoloft,
Allergien: Bee stings
Vorherige Impfungen: -

VAERS 1741016

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OR
Alter: 43,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 27.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Exposure during pregnancy Eye pain Fatigue Feeling cold Headache Pain Pain in extremity

Symptomtext

I woke up at 3 am with terrible head, body and eye pain. My right arm is very sore and cold feeling, and I am extremely tired. (more than normal even in pregnancy). I am currently 10 weeks pregnant, due date is 04/26/2022. My doctor advised a Tylenol regimen, which I began at 8am this morning. Symptoms are lessening, with the Tylenol, but I thought it important to report them.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroidism
Andere Medikamente: Levothyroxin, Lelothyronine and prenatal vitamin
Allergien: Bee allergy, Gluten allergy
Vorherige Impfungen: -

VAERS 1739941

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: NJ
Alter: 55,0
Geschlecht: M
Eingang: 28.09.2021
Impfdatum: -
Beginn: 21.09.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood glucose normal Cold sweat Dizziness Heart rate increased Blood glucose Blood pressure measurement Heart rate Vital signs measurement

Symptomtext

LIGHTHEADED FOR 15 MINUTES AFTER VACCINATION; FOREHEAD WAS CLAMMY; This spontaneous report received from a health care professional concerned a 55 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: gout, and rheumatoid arthritis, and other pre-existing medical conditions included: patient did not have allergies to medications, food or other products. The patient did not have any adverse event following any previous vaccine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A and expiry: UNKNOWN) dose was not reported, administered on 21-SEP-2021 10:45 for prophylactic vaccination. Concomitant medications included allopurinol. On 21-SEP-2021, the patient experienced lightheaded for 15 minutes after vaccination. On 21-SEP-2021, the patient experienced forehead was clammy. Laboratory data included: Blood glucose (NR: not provided) 132, Blood pressure (NR: not provided) normal, Heart rate (NR: not provided) elevated, and Vital signs measurement (NR: not provided) Stable. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from lightheaded for 15 minutes after vaccination, and forehead was clammy on 21-SEP-2021. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Date: 20210921; Test Name: Blood glucose; Result Unstructured Data: 132; Test Date: 20210921; Test Name: Vital signs measurement; Result Unstructured Data: Stable; Test Date: 20210921; Test Name: Heart rate; Result Unstructured Data: elevated; Test Date: 20210921; Test Name: Blood pressure; Result Unstructured Data: normal
Aktuelle Erkrankungen: Gout; Rheumatoid arthritis
Vorgeschichte: Comments: patient did not have allergies to medications, food or other products. The patient did not have any adverse event following any previous vaccine.
Andere Medikamente: ALLOPURINOL
Allergien: -
Vorherige Impfungen: -

VAERS 1739941

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: NJ
Alter: 55,0
Geschlecht: M
Eingang: 28.09.2021
Impfdatum: -
Beginn: 21.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood glucose normal Cold sweat Dizziness Heart rate increased Blood glucose Blood pressure measurement Heart rate Vital signs measurement

Symptomtext

LIGHTHEADED FOR 15 MINUTES AFTER VACCINATION; FOREHEAD WAS CLAMMY; This spontaneous report received from a health care professional concerned a 55 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: gout, and rheumatoid arthritis, and other pre-existing medical conditions included: patient did not have allergies to medications, food or other products. The patient did not have any adverse event following any previous vaccine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A and expiry: UNKNOWN) dose was not reported, administered on 21-SEP-2021 10:45 for prophylactic vaccination. Concomitant medications included allopurinol. On 21-SEP-2021, the patient experienced lightheaded for 15 minutes after vaccination. On 21-SEP-2021, the patient experienced forehead was clammy. Laboratory data included: Blood glucose (NR: not provided) 132, Blood pressure (NR: not provided) normal, Heart rate (NR: not provided) elevated, and Vital signs measurement (NR: not provided) Stable. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from lightheaded for 15 minutes after vaccination, and forehead was clammy on 21-SEP-2021. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Date: 20210921; Test Name: Blood glucose; Result Unstructured Data: 132; Test Date: 20210921; Test Name: Vital signs measurement; Result Unstructured Data: Stable; Test Date: 20210921; Test Name: Heart rate; Result Unstructured Data: elevated; Test Date: 20210921; Test Name: Blood pressure; Result Unstructured Data: normal
Aktuelle Erkrankungen: Gout; Rheumatoid arthritis
Vorgeschichte: Comments: patient did not have allergies to medications, food or other products. The patient did not have any adverse event following any previous vaccine.
Andere Medikamente: ALLOPURINOL
Allergien: -
Vorherige Impfungen: -

VAERS 1737527

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 27.09.2021
Impfdatum: 27.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cough Ear pruritus Injection site pruritus Injection site urticaria Joint swelling Peripheral swelling Pruritus Swollen tongue Throat irritation Urticaria

Symptomtext

Swollen tongue, hands, wrist, armpits, feet. Itchy throat/caugh, itchy wrists, palms, ears, buttocks, feet, armpits. Developed hives on wrists, armpits, buttocks, left arm around injection site. Received 1 shot left arm 09:30 A.M. first sign of reaction was itchiness left palm and injection site 1 minute after injection. Within 5 minutes itchiness spread to palms, wrists, ears, throat, feet, armpits, buttocks. After 5 minutes noticed swelling in hands, feet and tongue followed with hived around armpits, both wrists, buttocks, left arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid pos
Vorgeschichte: -
Andere Medikamente: Topamax, Zyrtex, Omeprazole
Allergien: -
Vorherige Impfungen: -

VAERS 1735462

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CO
Alter: 31,0
Geschlecht: M
Eingang: 26.09.2021
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: ja

Dizziness Hyperhidrosis Hypoaesthesia

Symptomtext

12:29PM/Janssen vaccine 0.5ml administered to L deltoid 12:36PM/patient reported while in observation area he "was feeling dizzy, like he was about to pass out" 12:36PM/patient was assisted to the ground with 2 EMT's , patient feet elevated Patient vitals 111/68, 58,22,96%02 SAT. patient diaphoretic, able to answer questions, NO LDC, patient reports left pinky finger numb which resolved quickly (approx 2 minutes) 12:39PM/cool water bottle placed under patient head, alcohol pad waved under patient nose, patient alert and oriented x 4. Decreased disphoresis, increase in patient color, patient reports feeling much better vitals 109/77, 71, 24, 95%O2 SAT. Cap refill 3 seconds. patient declined 9-1-1 or beevaluated by paramedics. pupils equla and reactive 12:45PM/ patient reports history of fainting with pain, patient reports mother also does this 12:48PM/patient assisted to sitting position on the ground. Vitals: 129/102, 86, 20, 95% 12:52pm/patient able to get up and sit in chair with standby assist if needed. patient able to perform independently vitals: 136/92, 78, 18, 96% O2 At 12:58PM/patient reports feeling good, continues to drink water. Patient agrees to stay another 10 minutes to assure he feels ok to drive 13:05PM/Vitals: 115/60, 55, 18, 96% Patient reports feeling good and reports he is fine to drive. Encouraged patient to contact PCP or go to Urgent Care if he develops further symptoms that are concerning. Discussed SOA, chest discomfort. If he develops these to seek emergency care. patient verbalized understanding and agrees with plan patient departed immediately after discussion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Denies
Vorgeschichte: Denies
Andere Medikamente: None
Allergien: Augmentin - N/V
Vorherige Impfungen: -

VAERS 1735068

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 24,0
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: unbekannt Erholt: ja

Dizziness

Symptomtext

Client immediately became light headed after vaccination. She was observed for additional 30 minutes with no additional symptoms reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: None reported
Allergien: NKA
Vorherige Impfungen: -

VAERS 1726166

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: GA
Alter: 50,0
Geschlecht: M
Eingang: 25.09.2021
Impfdatum: -
Beginn: 22.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Neck pain Nodule Oropharyngeal pain Bone pain Feeling abnormal Hypokinesia Injection site mass

Symptomtext

FELT LIKE SOMEONE INJECTED A LOT OF AIR INTO THE ARM; GOLF BALL SIZED MASS AT THE SITE OF INJECTION; PAIN IN THE LEFT COLLAR BONE LIKE SOMEBODY WHACKED IT; PAIN IN THE LEFT SIDE OF THE NECK / LEFT SIDE OF NECK STARTED TO FEEL LIKE PULLED MUSCLE; DIFFICULTY MOVING LEFT ARM; INTERMITTENT FEELING OF EXTREMELY SORE THROAT LIKE STEEL WOOL SCRATCHED INSIDE OF THROAT; This spontaneous report received from a patient concerned a 50 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: cholesterol issue, and other pre-existing medical conditions included: The patient did not have any change in lifestyle. The patient received covid-19 vaccine (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, administered on 22-SEP-2021 for prophylactic vaccination. Concomitant medications included acetylsalicylic acid for cholesterol issue, and atorvastatin for cholesterol issue. On 22-SEP-2021, the patient experienced felt like someone injected a lot of air into the arm. On 22-SEP-2021, the patient experienced golf ball sized mass at the site of injection. On 22-SEP-2021, the patient experienced pain in the left collar bone like somebody whacked it. On 22-SEP-2021, the patient experienced pain in the left side of the neck / left side of neck started to feel like pulled muscle. On 22-SEP-2021, the patient experienced difficulty moving left arm. On 22-SEP-2021, the patient experienced intermittent feeling of extremely sore throat like steel wool scratched inside of throat. The action taken with covid-19 vaccine was not applicable. The patient had not recovered from golf ball sized mass at the site of injection, pain in the left collar bone like somebody whacked it, pain in the left side of the neck / left side of neck started to feel like pulled muscle, difficulty moving left arm, and intermittent feeling of extremely sore throat like steel wool scratched inside of throat, and the outcome of felt like someone injected a lot of air into the arm was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood cholesterol abnormal
Vorgeschichte: Comments: The patient did not have any change in lifestyle.
Andere Medikamente: ATORVASTATIN; ASPRIN
Allergien: -
Vorherige Impfungen: -

VAERS 1731298

TEVA PHARMACEUTICALS · ADENOVIRUS TYPES 4 & 7, LIVE, ORAL (NO BRAND NAME) · Charge 211A21A

mild

Staat: CO
Alter: 23,0
Geschlecht: M
Eingang: 24.09.2021
Impfdatum: 23.09.2021
Beginn: 24.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Chest discomfort Chills Fear Heart rate increased Muscular weakness Myalgia Pyrexia

Symptomtext

Horrible fever, chills, and feeling of dread. Very weak muscles, sore muscles, and overall general weakness. Chest tightness and high heartbeat that felt like I was going to have a heart attack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1730166

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: 34,0
Geschlecht: M
Eingang: 24.09.2021
Impfdatum: -
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Cough Fatigue Oropharyngeal pain Pyrexia SARS-CoV-2 test Sinus congestion

Symptomtext

FELT REALLY TIRED; SORE THROAT; COUGHING; FELT CHILLS; POSSIBLE FEVER; SINUS CONGESTION; This spontaneous report received from a patient concerned a 34 year old male. The patient's weight was 210 pounds, and height was 71 inches. The patient's concurrent conditions included: non smoker, and alcohol user, and other pre-existing medical conditions included: The patient had no known drug or non-drug allergies and no history of drug abuse or illicit drug use. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, administered on 08-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On SEP-2021, the patient experienced sinus congestion. On 19-SEP-2021, the patient experienced sore throat. On 19-SEP-2021, the patient experienced coughing. On 19-SEP-2021, the patient experienced felt chills. On 19-SEP-2021, the patient experienced possible fever. On 20-SEP-2021, the patient experienced felt really tired. Laboratory data included: COVID-19 virus test (NR: not provided) Negative. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the sore throat, coughing, possible fever, felt chills, sinus congestion and felt really tired was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20210920; Test Name: COVID-19 virus test; Result Unstructured Data: Negative
Aktuelle Erkrankungen: Alcohol use (weekly maybe); Non-smoker
Vorgeschichte: Comments: The patient had no known drug or non-drug allergies and no history of drug abuse or illicit drug use.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1726618

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: OK
Alter: 48,0
Geschlecht: F
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: ja

Peripheral swelling Rash macular Urticaria

Symptomtext

Patient skin had red blotches like hives all over arms and hands/arms swelled. Notified the DOT Medical Examiner and check patient. In 15 minute wait time, symptoms went away. Patient denied having difficulty breathing. Epi-pen was not administered. Patient advised to take Benadryl, seek emergency care if symptoms reappear or worsen, and if she has any breathing problems.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash macular
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Denied any medications
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1723398

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: CA
Alter: 68,0
Geschlecht: M
Eingang: 22.09.2021
Impfdatum: 22.09.2021
Beginn: 22.09.2021
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

Symptomtext

Individual became lightheaded and diaphoretic a few minutes after receiving injection. He stated ?this happens to me when I get shots?. Vitals stable, no difficulty breathing or loss of consciousness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Denies
Vorherige Impfungen: -

VAERS 1723343

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cold sweat Headache Hypoaesthesia Injection site pain Urticaria

Symptomtext

Beginning at 3:15pm (9 minutes post vacc) Complaints of burning at injection site and over arm (left arm) Numbness down left arm Symptoms progressed at 3:28pm, to Cold Sweats Headache Urticaria of arms and legs Vitals: 140/82 blood pressure, 99 SpO2, 18 resp, 78 pulse, 97.8 temporal temp

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Ice pack to left arm, EMS called-Normal sinus rhythm -88 EMS recommended hospital transport but patient refused and signed AMA/refusal to transport
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Aspirin, ceftin
Vorherige Impfungen: -

VAERS 1723242

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: TX
Alter: 30,0
Geschlecht: M
Eingang: 22.09.2021
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Burning sensation Feeling hot Heart rate abnormal Hyperhidrosis Pain Sensation of foreign body Vision blurred

Symptomtext

Patient claimed to have felt very hot after receiving vaccine and feeling burning in arm. Patient claims to have been anxious about receiving vaccine also. Over a 5-10 minute period after receiving vaccine, patient claims to have felt lump in throat about size of acorn that grew larger, but claimed to have no difficulties breathing just a slight pain. He had visible sweating on forehead and also claimed to have blurry vision. Heart rate was monitored and dropped to the low 40's. No visible signs of swelling or redness were present on patient. Patient was given ice pack, water bottle and a fan to help cool off. Wife also came to sit near him. Patient began to improve with supportive care and heart rate increased to normal rates. Patient regained vision and claims lump felt in throat decreased. He was able to leave on his own with wife after about 40 minutes from receiving vaccine. Counseled to seek medical attention if symptoms worsened.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1722858

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

mild

Staat: WA
Alter: 61,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 21.09.2021
Beginn: 21.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Fatigue Pain

Symptomtext

Progressive (stabbing) joint pain in left side: shoulder, groin, thigh, chest, back; followed by extreme fatigue for over 24 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none so far
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Estogen, Progestone, Buspirone, Losartan
Allergien: none
Vorherige Impfungen: flu like symptoms to Shingles vaccine

VAERS 2661962

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 74,0
Geschlecht: M
Eingang: 27.07.2023
Impfdatum: 12.11.2021
Beginn: 13.01.2022
Tage bis Beginn: 62,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia COVID-19 Fall SARS-CoV-2 test positive

Symptomtext

Presented w c/o generalized weakness causing fall; incidental COVID-19+ finding, asymptomatic

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2615682

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: FL
Alter: 42,0
Geschlecht: M
Eingang: 15.04.2023
Impfdatum: 23.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient through other manufacturer (Pfizer Inc.) concerned a 44 year old male. Initial information was processed along with the additional information received on 13-APR-2023. The patient's height, and weight were not reported. The patient's concurrent conditions included: asthma, and penicillin allergy. The patient previously received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 205A21A expiry: UNKNOWN) dose was not reported, 1 total administered on 03-MAY-2021 to left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse events following covid-19 vaccine ad26.cov2.s (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211A21A expiry: UNKNOWN) dose was not reported, 1 total administered on 23-OCT-2021 to left arm for covid-19 prophylaxis. Age at time of vaccination 42 years old. Concomitant medications included salbutamol for unknown indication. On an unspecified date in 2023, the patient experienced covid-19 infection (Confirmed covid-19 Infection) (Dose number in series 2) for which patient received non-company suspect drug Paxlovid, (nirmatrelvir/ritonavir) (pill, route of admin, and batch number were not reported) dose and frequency were not reported from 24-MAR-2023 to 29-MAR-2023 for covid-19 treatment. Patient felt better 2 days after taking paxlovid and was tested negative on 29-MAR-2023 (last day of pills). On 04-APR-2023 10:00, 6 days after last dose patient felt stuffy and cough and tested positive which led to confirmed clinical vaccination failure (Dose number in series 2). On 29-MAR-2023, Laboratory data included: COVID-19 virus test Negative. On 04-APR-2023, Laboratory data included: COVID-19 virus test Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable; and action taken with nirmatrelvir/ritonavir was not reported. The patient had not recovered from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint: 90000278873.; Sender's Comments: V0: 20230425035- confirmed clinical vaccination failure . The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event. Specifically: SPECIAL SITUATIONS. Therefore, this event is considered inconsistent with vaccine administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230329; Test Name: COVID-19 TEST; Test Result: Negative ; Test Date: 20230404; Test Name: COVID-19 TEST; Test Result: Positive
Aktuelle Erkrankungen: Asthma; Penicillin allergy
Vorgeschichte: -
Andere Medikamente: ALBUTEROL [SALBUTAMOL]; PAXLOVID
Allergien: -
Vorherige Impfungen: -

VAERS 2518431

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WI
Alter: 54,0
Geschlecht: M
Eingang: 29.11.2022
Impfdatum: 19.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Unevaluable event

Symptomtext

None, Continues

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Fatigue, Asthenia, VZV, Inflammation
Andere Medikamente: Allopurinol, Diclofenac, Gabapentin
Allergien: None
Vorherige Impfungen: -

VAERS 2455970

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: MN
Alter: 50,0
Geschlecht: M
Eingang: 23.09.2022
Impfdatum: 22.09.2021
Beginn: 23.09.2022
Tage bis Beginn: 366,0
Dosis: N/A
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive

Symptomtext

Patient vaccinated against then tested positive for COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2370010

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: GA
Alter: 54,0
Geschlecht: M
Eingang: 15.07.2022
Impfdatum: 13.03.2022
Beginn: 01.05.2022
Tage bis Beginn: 49,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 54 year old male. Initial information was processed along with the additional information received on 08-JUL-2022. The patient's weight, height, and medical history were not reported. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 204B21A and expiry: unknown) dose was not reported, 1 total, administered on 13-DEC-2021 for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin, and batch number: 211A21A expiry: Unknown) dose was not reported, 1 total administered to left arm on 13-MAR-2022 for prophylactic vaccination. Age at time of vaccination 54 years old. No concomitant medications were reported. The patient was tested positive for Covid after 7 weeks (/MAY/2022) following booster vaccination and it was third time the patient tested positive which was coded as confirmed covid-19 infection (dose number in series 2) and confirmed clinical vaccination failure (dose number in series 2). The first time the patient was tested positive, where the test was received at his work place and then patient had a real test at the doctors office. The patient was sick for 5 days. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the confirmed clinical vaccination failure and confirmed covid-19 infection was not reported. This report was serious (Other Medically Important Condition). This case, from the same reporter is linked to 20220714463. This report was associated with a product quality complaint: 90000241155 and 90000241159.; Sender's Comments: V0:20220712200-COVID-19 VACCINE Ad26.COV2.S- confirmed clinical vaccination failure . The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202205; Test Name: COVID-19 VIRUS TEST; Test Result: Positive ; Test Name: COVID-19 VIRUS TEST; Test Result: Positive ; Test Name: COVID-19 VIRUS TEST; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2316373

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 11.06.2022
Impfdatum: 03.01.2022
Beginn: 28.05.2022
Tage bis Beginn: 145,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

COVID-19 TEST POSITIVE; This spontaneous report received from a consumer via other company manufacturer (Pfizer) concerned a 49 year old female. Initial information was processed along with the additional information received from department on 06-JUN-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: high blood pressure, migraines, and skin cancer. The patient previously received covid-19 vaccine ad26. cov2. s (unspecified manufacturer) (dose number in series 1) (suspension for injection, route of administration, batch number were not reported, expiry: unknown) dose was not reported, 1 total administered on an unspecified date for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26. cov2.s (dose number in series 1). The patient additionally received booster dose of covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: unknown) dose was not reported, 1 total administered on 03-JAN-2022 for prophylactic vaccination. Age at time of vaccination 48 years old. Concomitant medications included benzonatate, sumatriptan, and valsartan. On 20-MAY-2022, the patient started non-company suspect drug Paxlovid for treatment of COVID-19. Paxlovid was discontinued on 24-MAY-2022. On 28-MAY-2022, the patient returned to positive rapid test after four negative days. (dose number in series 2). Laboratory data included: COVID-19 rapid POC test Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable and with Paxlovid was drug discontinued. The outcome of covid-19 was not reported. This report was non-serious. This report was associated with product quality complaint: 90000234203.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20220528; Test Name: COVID-19 RAPID POC TEST; Test Result: Positive
Aktuelle Erkrankungen: Blood pressure high; Migraine; Skin cancer
Vorgeschichte: -
Andere Medikamente: VALSARTAN; BENZONATATE; SUMATRIPTAN
Allergien: -
Vorherige Impfungen: -

VAERS 2292791

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: KS
Alter: 66,0
Geschlecht: M
Eingang: 24.05.2022
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Interchange of vaccine products

Symptomtext

Patient's first dose was Pfizer & he did not complete the series because his second dose on 11/12/2021 was Janssen not Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: UNKNOWN.
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: Bactrim, Cephalexin, Lipitor
Vorherige Impfungen: -

VAERS 2231280

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 13.04.2022
Impfdatum: 11.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Confusional state Disturbance in attention Feeling abnormal Head discomfort Laboratory test normal Loss of personal independence in daily activities Memory impairment Mental impairment Neurological symptom Night blindness Personality change

Symptomtext

2 weeks after the vaccine, I was having brain fogginess. I was feeling heaviness in my brain. I felt really full in my head, like I was about to have a stroke. I felt like it was no oxygen going to brain, I cannot focus. I cannot focus and pay attention. I have a slow thinking, confusion, unable to concentrate. I had flunked my exam because I could not think or focus to take my test. I want to ask my doctor to give me an MRI, or CT of my Brain. My ability to think and concentrate is altered. I have a difficulty remembering things now. I feel like a slow thinker. I was doing okay and writing programs and now I cannot study, it's so difficult to remember things. I feel altered in my personality as well. I have to sleep to rid of the heaviness, I have to sleep and wake up with the fullness in my head. I wake up not remembering why I am moving or what I was going to do. No my vision is also worse, I have changed glasses twice and I cannot see at night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Confusional state
Hospital-Tage: -
Labordaten: 10/2021 - Lab Work Pre and Post - It was Normal
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth Control - Trinessa
Allergien: Lactose Intolerant
Vorherige Impfungen: Flu Vaccine 13 years ago. at 40 years old. I got sick and almost fainted. I could not get up, I was weak and had to take two wee

VAERS 2201670

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 33,0
Geschlecht: M
Eingang: 28.03.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Product storage error

Symptomtext

Pt was given vaccine on 12/16/2021 which had expiration date of 12/14/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2201661

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 37,0
Geschlecht: M
Eingang: 28.03.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Vaccine given on 12/16/2021 had expiration date of 12/14/2021. Pt had no know adverse reaction to this error.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2192178

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 55,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192177

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192174

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 44,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192171

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 52,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Product storage error

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192170

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Product storage error

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192168

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Product storage error

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192130

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 58,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Product storage error

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192127

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 19,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Product storage error

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192124

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Product storage error

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192121

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Product storage error

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192118

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Product storage error

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192116

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Product storage error

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192113

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 32,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Product storage error

Symptomtext

Patient was administered vaccine beyond the published expiration date. Per Janssen Manufacturer, re-vaccination is not required, the vaccine was determined to still maintain the activity necessary to protect against Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2184261

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

gering

Staat: TX
Alter: 57,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 03.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Tinnitus

Symptomtext

tinnitus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: factor V Leiden
Andere Medikamente: Xarelto, zinc, vitamin d, omega 3
Allergien: none
Vorherige Impfungen: -

VAERS 2174787

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

gering

Staat: TX
Alter: 56,0
Geschlecht: M
Eingang: 12.03.2022
Impfdatum: -
Beginn: 06.03.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

SARS-CoV-2 test Suspected COVID-19

Symptomtext

SUSPECTED COVID-19; This spontaneous report received from a patient concerned a 57 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: the patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211a21a, expiry: UNKNOWN) dose was not reported, administered on 22-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On 06-MAR-2022, the patient experienced suspected covid-19. On 07-MAR-2022, Laboratory data included: SARS-CoV-2 test (not provided) negative. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from suspected covid-19. This report was non-serious.; Sender's Comments: Medical assessment comment not required as per standard procedure as the case was assessed as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20220307; Test Name: SARS-CoV-2 test; Result Unstructured Data: negative; Comments: test kit- JNJ home supplied binax now test kit
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: the patient had no known allergies
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2171072

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 34,0
Geschlecht: M
Eingang: 10.03.2022
Impfdatum: 10.03.2022
Beginn: 10.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

No adverse event Product storage error

Symptomtext

NO ADVERSE REACTION, DOSE GIVEN WAS ONE DAY OUT OF DATE

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2168332

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: OR
Alter: 68,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Product storage error

Symptomtext

Patient was given vaccine that had expired (12/14/2021) the day prior to injection on 12/15/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None stated
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2160670

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

TESTED POSITIVE TWICE FOR COVID; This spontaneous report received from a patient concerned a 56 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, administered on 13-SEP-2021 for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On 01-MAR-2022, Laboratory data included: COVID-19 antigen test (NR: not provided) Twice positive. On an unspecified date, the patient experienced tested positive twice for covid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of tested positive twice for covid was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20220301; Test Name: COVID-19 antigen test; Result Unstructured Data: Twice positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160668

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: -
Beginn: 17.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED UNINTENTIONALLY; This spontaneous report received from a pharmacist concerned a 40 year old female of an unspecified race and ethnic origin. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient had no illness at time of vaccination. Patient had no past history of similar event. Patient had no adverse event after any previous vaccination(s). Patient had no history of allergy to vaccine, drug, or food. Patient had no pre-existing acute illness 30 days prior to vaccination. Patient had no history of hospitalization in last 30 days, with cause. Patient had no family history of any disease (relevant to vaccination) or allergy. Patient was not pregnant at the time of vaccination. Patient was not currently breastfeeding. The patient previously received covid-19 vaccine ad26. cov2.s (suspension for injection, intramuscular, batch number: 1805018, and expiry: unknown) dose was not reported, (Dose number in series 01), 01 in total was administered on 23-MAR-2021 for prophylactic vaccination. No adverse events were reported following vaccination with covid-19 vaccine ad26. cov2.s (Dose number in series 01). The patient additionally received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, (Dose number in series 02), 01 in total was administered on 17-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 17-DEC-2021, expired vaccine was administered unintentionally (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered unintentionally was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382, 20220261011, 20220261063, 20220261042, 20220261024, 20220261048, 20220261000, 20220261039, 20220260967, 20220261022, 20220261030, 20220260995, 20220261014 and 20220261043.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no illness at time of vaccination. Patient had no past history of similar event. Patient had no adverse event after any previous vaccination(s). Patient had no history of allergy to vaccine, drug, or food. Patient had no pre-existing acute illness 30 days prior to vaccination. Patient had no history of hospitalization in last 30 days, with cause. Patient had no family history of any disease (relevant to vaccination) or allergy. Patient was not pregnant at the time of vaccination. Patient was not currently breastfeeding.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160667

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 46,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: -
Beginn: 16.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned a 46 year old male of unspecified age, race and ethnic origin. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient had no illness at the time of vaccination and no history of similar event, no history of adverse event after any previous vaccination, no pre-existing acute illness 30 days prior to vaccination, no History of hospitalization in last 30 days. Patient had no history of allergy to vaccine, drug, or food and no family history of any disease (relevant to vaccination) or allergy. On 23-MAR-2021, The patient was previously treated with covid-19 vaccine ad26. cov2.s (Dose number in series 1) (suspension for injection, intramuscular, batch number: 1805018 and expiry date: unknown) dose was not reported, 1 total, administered on 23-MAR-2021 on right side for prophylactic vaccination. No adverse events reported following vaccination. It was unspecified whether patient had any adverse reaction following primary vaccination (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, (Dose number in series 2) 1 total, administered On 16-DEC-2021 on right side for prophylactic vaccination. No concomitant medications were reported. On 16-DEC-2021, the patient administered expired vaccine (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382, 20220261011, 20220261039, 20220261092, 20220260967, 20220261043, 20220261022, 20220261000, 20220261030, 20220260995 and 20220261042, 20220261024, 20220261048, 20220261014.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no illness at the time of vaccination and no history of similar event, no history of adverse event after any previous vaccination, no pre-existing acute illness 30 days prior to vaccination, no History of hospitalization in last 30 days. Patient had no history of allergy to vaccine, drug, or food and no family history of any disease (relevant to vaccination) or allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160666

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 52,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: -
Beginn: 21.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned a 52 year old male of unspecified race and ethnic origin. The patient's height, and weight were not reported. Patient did not report any illness at the time of vaccination. Patient had no history of similar event, had no adverse events related to previous vaccinations, no history of allergy to vaccine, drug, or food. Patient did not report any history of pre-existing acute illness 30 days prior to vaccination. Patient had no history of hospitalization and had no family history of any disease. On 29-APR-2021, the patient was previously vaccinated with covid-19 vaccine ad26. cov2.s (dose number in series: 1) (suspension for injection, intramuscular, batch number 1805029, expiry: unknown) 1 total, to left arm for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with covid-19 vaccine ad26. cov2.s (dose number in series: 1). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series: 2) (suspension for injection, intramuscular, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, 1 total, administered to the left arm on 21-DEC-2021 for prophylactic vaccination. The vaccine was stored at 2-8 degrees Celsius. The vaccine was removed thrice from the storage and kept out for 10 minutes. Then returned to refrigerator. The gauze/length of the needle was 25G, 1 inch. No concomitant medications were reported. On 21-DEC-2021, the patient received expired vaccine (Dose number in series: 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382, 20220260967, 20220261000, 20220261011, 20220261042, 20220261024, 20220261063, 20220261039, 20220261092, 20220261014 and 20220260995.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient did not report any illness at the time of vaccination. Patient had no history of similar event, had no adverse events related to previous vaccinations, no history of allergy to vaccine, drug, or food. Patient did not report any history of pre-existing acute illness 30 days prior to vaccination. Patient had no history of hospitalization and had no family history of any disease.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160665

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: -
Beginn: 16.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned a 70 year old female of unspecified race and ethnic origin. The patient's height, and weight were not reported. The patient's concurrent conditions included: drug allergy (ciprofloxacin allergy), and other pre-existing medical conditions included: Patient had no illness at time of vaccination, no past history of similar event, no adverse event after any previous vaccination(s). Patient had no pre-existing acute illness 30 days prior to vaccination, no history of hospitalization in last 30 days, with cause. Patient had no family history of any disease (relevant to vaccination) or allergy. Patient was not pregnant and was not breastfeeding at the time of vaccination. The patient previously received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 042A21A, expiry: Unknown) dose was not reported, dose number in series 1, 01 in total, administered on 30-MAR-2021 in left arm for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, dose number in series 2, 01 in total, administered on 16-DEC-2021 in left arm for prophylactic vaccination. No concomitant medications were reported. On 16-DEC-2021, the patient administered expired vaccine (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382, 20220260967, 20220261011, 20220261063, 20220261042, 20220261024, 20220261000, 20220261092, 20220261014 and 20220261030.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (ciprofloxacin allergy)
Vorgeschichte: Comments: Patient had no illness at time of vaccination, no past history of similar event, no adverse event after any previous vaccination(s). Patient had no pre-existing acute illness 30 days prior to vaccination, no history of hospitalization in last 30 days, with cause. Patient had no family history of any disease (relevant to vaccination) or allergy. Patient was not pregnant and was not breastfeeding at the time of vaccination.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160664

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 19,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: -
Beginn: 27.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned a 19 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient had no illness at the time of vaccination, no history of similar events, no adverse event after any previous vaccination(s), no any food, drug, or vaccine history allergy, no any pre-existing acute illness 30 days prior to vaccination, no history of hospitalization in last 30 days with cause and had no family history of any disease (relevant to vaccination) or allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, administered on 27-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 27-DEC-2021, the patient experienced expired vaccine administered. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20220260967, 20220261014, 20220261042, 20220260995, 20220261011, 20220261030, 20220261048, 20220261000, 20220261022, 20220261024, 20220261043, 20220261039, 20220261063, 20220261092 and 20220210382.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no illness at the time of vaccination, no history of similar events, no adverse event after any previous vaccination(s), no any food, drug, or vaccine history allergy, no any pre-existing acute illness 30 days prior to vaccination, no history of hospitalization in last 30 days with cause and had no family history of any disease (relevant to vaccination) or allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160663

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 79,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned a 79 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient was not having any illness at the time of vaccination. patient had no history of similar events, had no adverse event after any previous vaccination(s). The patient had no history of allergy to food, drug, or vaccine, had no pre-existing acute illness 30 days prior to vaccination, had no history of hospitalization in last 30 days. The patient was not having any family history of any disease (relevant to vaccination) or allergy. The patient was not pregnant nor breastfeeding at the time of vaccination. The patient was previously treated with covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, intramuscular, batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered 1 in total, to the right on 11-AUG-2021 for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, intramuscular, batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered 1 in total to the left on 16-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 16-DEC-2021, the patient experienced expired vaccine administered (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient was not having any illness at the time of vaccination. patient had no history of similar events, had no adverse event after any previous vaccination(s). The patient had no history of allergy to food, drug, or vaccine, had no pre-existing acute illness 30 days prior to vaccination, had no history of hospitalization in last 30 days. The patient was not having any family history of any disease (relevant to vaccination) or allergy. The patient was not pregnant nor breastfeeding at the time of vaccination.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160662

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 44,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: -
Beginn: 22.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned a 44 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient had no illness at time of vaccination. Patient had no past history of similar event. Patient had no adverse event after any previous vaccination(s). Patient had no history of allergy to vaccine, drug, or food. Patient had no pre-existing acute illness 30 days prior to vaccination. Patient had no history of hospitalization in last 30 days, with cause. Patient had no family history of any disease (relevant to vaccination) or allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 22-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 22-DEC-2021, the patient experienced expired vaccine administered. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382, 20220260967, 20220261011, 20220261063, 20220261042, 20220261024 and 20220261092.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no illness at time of vaccination. Patient had no past history of similar event. Patient had no adverse event after any previous vaccination(s). Patient had no history of allergy to vaccine, drug, or food. Patient had no pre-existing acute illness 30 days prior to vaccination. Patient had no history of hospitalization in last 30 days, with cause. Patient had no family history of any disease (relevant to vaccination) or allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160661

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: -
Beginn: 15.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned a 57 year old female of unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no history of similar event, had no illness at the time of vaccination. The patient had no adverse event after any previous vaccination, no history of allergy to vaccine, drug or food, had no pre-existing acute illness 30 days prior to vaccination, no history of hospitalization in last 30 days, no family history of any disease or allergy. The patient was not pregnant at time of vaccination and was not currently breastfeeding. The patient was previously received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, intramuscular, batch number: 1808978, and expiry: unknown) dose was not reported, 1 total, administered on 09-APR-2021 on left site for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26.cov2.s.(Dose number in series 1). The patient additionally received booster covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, intramuscular, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, 1 total administered on 15-DEC-2021 on left site for prophylactic vaccination. No concomitant medications were reported. On 15-DEC-2021, the patient was administered with expired vaccine (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382, 20220260967, 20220261011, 20220261042, 20220261039, 20220261092, 20220261043, 20220261022, 20220261000, 20220261048, 20220260995, 20220261014, 20220261063 and 20220261030.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no history of similar event, had no illness at the time of vaccination. The patient had no adverse event after any previous vaccination, no history of allergy to vaccine, drug or food, had no pre-existing acute illness 30 days prior to vaccination , no history of hospitalization in last 30 days, no family history of any disease or allergy. The patient was not pregnant at time of vaccination and was not currently breastfeeding.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160660

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: -
Beginn: 15.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned a 32 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: patient was not having any illness at the time of vaccination. patient was not having any history of similar events. patient was not having adverse event after any previous vaccination(s). patient was not having any food, drug, or vaccine allergy. patient was not having any pre-existing acute illness 30 days prior to vaccination. patient was not having the history of hospitalization in last 30 days. patient was not having any family history of any disease (relevant to vaccination) or allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, administered on 15-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 15-DEC-2021, the patient experienced expired vaccine administered. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: patient was not having any illness at the time of vaccination. patient was not having any history of similar events. patient was not having adverse event after any previous vaccination(s). patient was not having any food, drug, or vaccine allergy. patient was not having any pre-existing acute illness 30 days prior to vaccination. patient was not having the history of hospitalization in last 30 days. patient was not having any family history of any disease (relevant to vaccination) or allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160659

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned a 28 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no illness at the time of vaccination, no history of similar event, no adverse event after any previous vaccination (s), no history of allergy to vaccine, drug, or food, no pre-existing acute illness 30 days prior to vaccination, no history of hospitalization in last 30 days, with cause and no family history of any disease (relevant to vaccination) or allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered on 27-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 27-DEC-2021, the patient experienced expired vaccine administered. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382, 20220260967, 20220261042, 20220261011, 20220261063, 20220261048, 20220261092, 20220261039, 20220261022, 20220261000, 20220261030, 20220260995, 20220261043 and 20220260995.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no illness at the time of vaccination, no history of similar event, no adverse event after any previous vaccination (s), no history of allergy to vaccine, drug, or food, no pre-existing acute illness 30 days prior to vaccination, no history of hospitalization in last 30 days, with cause and no family history of any disease (relevant to vaccination) or allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160658

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: -
Beginn: 23.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned a 38 year old female of unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no illness at the time of vaccination, no past history of similar events, no adverse event after any previous vaccination, no history of allergy to vaccine drug or food, no pre-existing acute illness 30 days prior to vaccination, no history of hospitalization in last 30 days, with cause, no family history of any disease (relevant to vaccination) or allergy, not pregnant at time of vaccination and not currently breastfeeding. The patient previously received covid-19 vaccine ad26. cov2.s (dose number in series 1) (suspension for injection, intramuscular and batch number: 201A21A, expiry: unknown) dose was not reported, 1 total, administered on 22-May-2021 on left (location unspecified) for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26. cov2.s (dose number in series 1). The patient additionally received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, intramuscular, and batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, 1 total administered on 23-DEC-2021 on left (location unspecified) for prophylactic vaccination. No concomitant medications were reported. On 23-DEC-2021, the patient received expired vaccine administered (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382, 20220261039, 20220261092, 20220261063, 20220260967, 20220261043, 20220261022, 20220261030, 20220261000, 20220261048, 20220261014, 20220260995, 20220261024 and 20220261042.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no illness at the time of vaccination, no past history of similar events, no adverse event after any previous vaccination, no history of allergy to vaccine drug or food, no Pre-existing acute illness 30 days prior to vaccination, no History of hospitalization in last 30 days, with cause, no family history of any disease (relevant to vaccination) or allergy, not pregnant at time of vaccination and not Currently breastfeeding.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160657

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: -
Beginn: 20.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned a 57 year old female of unspecified race and ethnic origin. The patient's height, and weight were not reported. Patient did not report any illness at the time of vaccination. Patient had no history of similar event, had no adverse events related to previous vaccinations, no history of allergy to vaccine, drug, or food. Patient did not report any history of pre-existing acute illness 30 days prior to vaccination. Patient had no history of hospitalization and had no family history of any disease. Patient was not pregnant nor breastfeeding at the time of reporting. On 14-JUN-2021, the patient was previously vaccinated with covid-19 vaccine ad26. cov2.s (dose number in series: 1) (suspension for injection, intramuscular, batch number: 203A21A and Expiry: Unknown) 1 total, to left arm for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with covid-19 vaccine ad26. cov2.s (dose number in series: 1). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series: 2) (suspension for injection, intramuscular, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, 1 total, administered to right arm on 20-DEC-2021 for prophylactic vaccination. Vaccine was administered to right arm. The vaccine was stored at 2-8 degrees Celsius. The vaccine was removed thrice from the storage and kept out for 10 minutes. Then returned to refrigerator. The gauze/length of the needle was 25G, 1 inch. No concomitant medications were reported. On 20-DEC-2021, the patient received expired vaccine (Dose number in series: 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382, 20220260967, 20220261048, 20220261011, 20220261063, 20220261042, 20220261024, 20220261039, 20220261092, 20220261043 and 20220261022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient did not report any illness at the time of vaccination. Patient had no history of similar event, had no adverse events related to previous vaccinations, no history of allergy to vaccine, drug, or food. Patient did not report any history of pre-existing acute illness 30 days prior to vaccination. Patient had no history of hospitalization and had no family history of any disease. Patient was not pregnant nor breastfeeding at the time of reporting.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160656

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 55,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: -
Beginn: 23.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED UNINTENTIONALLY; This spontaneous report received from a pharmacist concerned a 55 years old male patient of an unspecified race and ethnic origin. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient had no Illness at the time of vaccination, no history of similar event, no adverse event after any previous vaccination, no history of allergy to vaccine, drug, or food, no pre-existing acute illness 30 days prior to vaccination, no history of hospitalization in last 30 days with cause, no family history of any disease (relevant to vaccination) or allergy. The patient previously received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 201A21A, expiry: Unknown) dose was not reported, dose number in series 1, 01 total, administered on left arm on 09-JUN-2021 for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient additionally received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, dose number in series 2, 01 total, administered on right arm on 23-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 23-DEC-2021, expired vaccine was administered unintentionally (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered unintentionally was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382, 20220260967, 20220261042, 20220261063, 20220261011, 20220261024, 20220261048, 20220261092 and 20220261014. .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no Illness at the time of vaccination, no history of similar event, no adverse event after any previous vaccination, no history of allergy to vaccine, drug, or food, no pre-existing acute illness 30 days prior to vaccination, no history of hospitalization in last 30 days, with cause, no family history of any disease (relevant to vaccination) or allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2160655

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 53,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned a 53 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient had no illness at the time of vaccination and no history of similar event. Patient had no adverse event after any previous vaccination(s). Patient had no history of allergy to vaccine, drug, or food. Patient had no pre-existing acute illness 30 days prior to vaccination. Patient had no history of hospitalization in last 30 days, with cause. Patient had no family history of any disease (relevant to vaccination) or allergy. The patient previously received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, intramuscular, batch number: 1805029 expiry: Unknown) dose was not reported, 1 total, administered on 13-MAR-2021 in left arm for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26.cov2.s (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, intramuscular, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, 1 total, administered on 20-DEC-2021 in right arm for prophylactic vaccination. No concomitant medications were reported. On 20-DEC-2021, the patient was administered expired vaccine (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20220210382, 20220260995, 20220261000, 20220261014, 20220261024, 20220261030, 20220261042, 20220261043, 20220261048, 20220261011 and 20220261063.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no illness at the time of vaccination and no history of similar event. Patient had no adverse event after any previous vaccination(s). Patient had no history of allergy to vaccine, drug, or food. Patient had no pre-existing acute illness 30 days prior to vaccination. Patient had no history of hospitalization in last 30 days, with cause. Patient had no family history of any disease (relevant to vaccination) or allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2157854

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 07.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 36,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Colostomy Diverticulitis Intestinal resection Laparoscopy abnormal Large intestine anastomosis

Symptomtext

Diverticulitis of large intestine without bleeding; procedure - elective sigmoid resection on 11/12/21. She was brought back to the operating room and underwent diagnostic laparoscopy with takedown of anastomosis and creation of end descending colon colostomy. Discharged after treatment. Hospital visit was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Colostomy
Hospital-Tage: 17,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2129187

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WI
Alter: 45,0
Geschlecht: F
Eingang: 21.02.2022
Impfdatum: 29.10.2021
Beginn: 10.02.2022
Tage bis Beginn: 104,0
Dosis: 2
Route/Site: IM / RA

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: -

VAERS 2118395

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 52,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

SARS-CoV-2 test Suspected COVID-19 Vaccination failure

Symptomtext

SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 52 year old male of unspecified ethnic origin. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient was previously treated with BNT 162 (Pfizer) (Dose number in series:1) (form of admin, route of admin not reported, batch number: EN6208,expiry: unknown) dose was not reported, administered on 02-MAR-2021 for prophylactic vaccination, (form of admin, route of admin not reported, batch number: EM9810 ,expiry: unknown) dose was not reported, administered on 02-APR-2021 for prophylactic vaccination. No adverse event was reported with BNT 162 (Pfizer) (Dose number in series:1). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series:2) (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, 1 total administered on 19-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 10-FEB-2022, the patient experienced suspected covid-19 infection and patient tested with Binax Now test (suspected clinical vaccination failure) and Laboratory data included: COVID-19 rapid POC test (NR: not provided) Positive (Dose number in series:2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the suspected covid-19 infection and suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint, and reference number was requested.; Sender's Comments: V0: 20220229470- covid-19 vaccine ad26.cov2.s-Suspected clinical vaccination failure. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20220210; Test Name: COVID-19 rapid POC test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115645

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21a

gering

Staat: FL
Alter: 49,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: -
Beginn: 01.02.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Nasopharyngitis

Symptomtext

DRY COUGH; COLD; This spontaneous report received from a patient concerned a 49 year old White, Not Hispanic/Latino male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26. cov2. s (dose number in series 1) (suspension for injection, route of admin not reported and batch number: 1808609 and expiry: unknown) dose was not reported, 1 total, administered at right arm on 27-MAY-2021 for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26. cov2.s (dose number in series 1). The patient received booster covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211A21a and expiry: unknown) dose was not reported, 1 total, administered at right arm on 16-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date in FEB-2022, the patient experienced dry cough and cold (all events with dose number in series 2). It was reported that patient had not been tested for covid, and suffering from cold for last week and thought dry cough was due to cold remnants but agent reporting any symptoms out of an abundance of caution. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the dry cough and cold was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cough
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2101090

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: -
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: -
Beginn: 14.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered SARS-CoV-2 test Suspected COVID-19

Symptomtext

SYMPTOMS OF COVID; EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a patient concerned a 59 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and batch number: 211A21A expiry: 14/DEC/2021) dose was not reported, administered on 14-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-DEC-2021, the patient experienced expired vaccine administered. On 07-FEB-2022, Laboratory data included: COVID-19 virus test (NR: not provided) negative. On an unspecified date, the patient experienced symptoms of covid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the symptoms of covid and expired vaccine administered was not reported. This report was non-serious.; Sender's Comments: V0: Medical Assessment Comment not required as per standard procedure as case assessed as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: Test Date: 20220207; Test Name: COVID-19 virus test; Result Unstructured Data: negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2099735

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: AZ
Alter: 49,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 11.10.2021
Beginn: 11.11.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Biopsy breast Breast mass Computerised tomogram neck Neck mass Ultrasound scan

Symptomtext

I DEVELOPED A LARGE LUMP ON THE LEFT SIDE OF MY NECK ON MY CAROTID ARTERY AND NECK MUSCLE AREA ON 11/11/2021 THAT FLARES UP DURING THE DAY WHEN I USE MY ARM A LOT WITH ANYTHING I DO, THAT IS THE SAME SIDE OF THE ARM I RECEIVED THE VACCINE AND NOW IT IS ON THE OTHER SIDE OF MY NECK. I HAVE HAD A US SOFT TISSUE NECK ON 11/16/2021, AND CT NECK WITHOUT CONTRAST AND WAS TOLD BY MY RAD WHERE I WORK THAT IT IS DEFINATELY RELATED TO THE VACCINE AND BREAST BIOPSY I HAD TO GET DUE TO LUMP ON MY BREAST ON 11/11/2021. LUMP APPEARED IMMEDIATELY AFTER MY BREAST BIOPSY 2 HOURS AFTER THE PROCEDURE AND STILL REMAINS VISIBLE ON MY NECK BOTH SIDES.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Biopsy breast
Hospital-Tage: -
Labordaten: I SAW MY DR ON 11/12/21 THE NEXT DAY AND HE ORDERED SOME LABES AND TWO TEST. I HAD A US SOFT TISSUE NECK ON 11/16/2021, AND CT NECK WITHOUT CONTRAST ON 11/18/21 AND WAS TOLD BY MY RAD WHERE I WORK THAT IT IS DEFINATELY RELATED TO THE VACCINE AND BREAST BIOPSY I HAD TO GET DUE TO LUMP ON MY BREAST ON 11/10/2021. LUMP APPEARED IMMEDIATELY AFTER MY BREAST BIOPSY 2 HOURS AFTER THE PROCEDURE AND STILL REMAINS VISIBLE ON MY NECK BOTH SIDES AND HURTS FROM TIME TO TIME DEPENDING ON MY ACTIVITIES.
Aktuelle Erkrankungen: N/A - NONE
Vorgeschichte: NONE.
Andere Medikamente: ASPRIN 200 MG, PEDIALYTE AND EMERGEN-C
Allergien: NONE. ONLY CT CONTRAST DYE
Vorherige Impfungen: -

VAERS 2098220

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

gering

Staat: CA
Alter: -
Geschlecht: U
Eingang: 09.02.2022
Impfdatum: -
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE ADMINISTERED; This spontaneous report received from a pharmacist concerned multiple patients. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A and expiry: 14/DEC/2021) dose was not reported, administered on DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On DEC-2021, the patient experienced expired vaccine administered. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2087112

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19

Symptomtext

COVID AFTER RECEIVING THE JANSSEN COVID 19 VACCINE; This spontaneous report received from a patient concerned a 42 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 25-AUG-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced covid after receiving the janssen covid 19 vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of covid after receiving the janssen covid 19 vaccine was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2075049

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 30.01.2022
Impfdatum: 17.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Interchange of vaccine products Vaccine breakthrough infection

Symptomtext

Fully vaccinated with J&J. Boosted on 1/17/22. COVID infection breakthrough with inpatient stay

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2074147

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 29.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Suspected COVID-19

Symptomtext

SYMPTOMS OF COVID; This spontaneous report received from a patient concerned a 21 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A and expiry: 14-DEC-2021) dose was not reported, administered on 22-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced symptoms of covid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of symptoms of covid was not reported. This report was non-serious. This case, from the same reporter is linked to 20220150408 and 20220151154.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Suspected COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2071556

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

TESTED POSITIVE FOR COVID; This spontaneous report received from a consumer concerned a 50 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, administered on 22-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced tested positive for covid. Laboratory data (dates unspecified) included: COVID-19 virus test (not provided) Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of tested positive for covid was not reported. This report was non-serious. This case, from the same reporter is linked to 20220150408 and 20220150229.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Name: COVID-19 virus test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2071106

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Suspected COVID-19

Symptomtext

HAVING SYMPTOMS OF COVID AFTER RECEIVING THE JANSSEN COVID 19 VACCINE; This spontaneous report received from a consumer concerned a 21 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered on 22-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced having symptoms of covid after receiving the janssen covid 19 vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of having symptoms of covid after receiving the janssen covid 19 vaccine was not reported. This report was non-serious. This case, from the same reporter is linked to 20220150229.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Suspected COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2067692

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

COVID AFTER RECEIVING THE JANSSEN COVID-19 VACCINE (COVID-19 TEST POSITIVE); This spontaneous report received from a patient concerned a 27 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered on 08-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced covid after receiving the janssen covid-19 vaccine (covid-19 test positive). Laboratory data (dates unspecified) included: COVID-19 rapid POC test (NR: not provided) Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of covid after receiving the janssen covid-19 vaccine (covid-19 test positive) was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Name: COVID-19 rapid POC test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2065772

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TN
Alter: 26,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 13.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dysmenorrhoea Heavy menstrual bleeding Menstruation irregular

Symptomtext

Change in menstrual cycle. Within 5 days of vaccine, 1st menstrual cycle (bleeding) started. That menstrual cycle was 2 weeks early. Menstrual cycle has since occurred every other week, with bleeding lasting about 5 days each time. So 5 days actively bleeding, roughly 10 days not bleeding in between, and then cycle begins again. Menstrual cycle previously averaged every 28 days for at least 5 years consistently. Cycle is now increasingly more painful, heavy, passing clots, etc.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dysmenorrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2075280

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WI
Alter: 41,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Antinuclear antibody C-reactive protein Full blood count Metabolic function test Peripheral coldness Red blood cell sedimentation rate Skin discolouration

Symptomtext

Within 24-48 hours of vaccine patient developed a sensation that his finger was cold & turned white. This comes & goes but happen about 1/wk

Weitere VAERSDATA-Felder

Praegender Schweregrund: Antinuclear antibody
Hospital-Tage: -
Labordaten: CRP, Sed rate, CBC, CMP, ANA, Urine ordered
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2058730

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: MN
Alter: 78,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 10.11.2021
Beginn: 22.01.2022
Tage bis Beginn: 73,0
Dosis: 2
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

hospitalized with a breakthrough COVID 19 infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 2,0
Labordaten: 1/17/22- SARS Coronavirus-2, PCR detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2053704

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: FL
Alter: 37,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: -
Beginn: 17.01.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

SARS-CoV-2 test Suspected COVID-19 Vaccination failure

Symptomtext

SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 37 year old male. Initial information was processed with the additional information received on 18-JAN-2022. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, 1 total, administered on 21-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On 17-JAN-2022, the patient had suspected clinical vaccination failure and suspected covid-19 infection (symptoms of sore throat, stuffy nose, headache and body ache). Laboratory data included: COVID-19 rapid test (NR: not provided) was positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from suspected covid-19 infection and suspected clinical vaccination failure. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint: 90000212145.; Sender's Comments: V0-20220130118-COVID-19 VACCINE AD26.COV2.S- Suspected clinical vaccination failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20220117; Test Name: COVID-19 rapid POC test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2053696

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: -
Beginn: 13.01.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

SARS-CoV-2 test Suspected COVID-19 Vaccination failure

Symptomtext

SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 55 year old Hispanic or Latino female. Initial information was processed along with the additional information received on 14-JAN-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: allergy. The patient previously received covid-19 vaccine ad26. cov2. s (Dose number in series 1) (suspension for injection, route of admin not reported, and batch number: 1808980, expiry: Unknown) dose was not reported, 1 total administered to right arm on 06-MAY-2021 for prophylactic vaccination. No adverse events were reported following vaccination with covid-19 vaccine ad26. cov2. s. (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of admin not reported, and batch number: 211A21A expiry: UNKNOWN) dose was not reported, 1 total administered to right arm on 05-NOV-2021 for prophylactic vaccination. The patient used to take medicine for allergy. On 13-JAN-2021, following vaccination with covid-19 vaccine ad26.cov2.s, the patient experienced sore throat, runny nose, headache, loss of taste and felt it may be due to covid (coded as suspected covid-19 infection, suspected clinical vaccination failure) (Dose number in series 2). Laboratory data included: COVID-19 PCR (polymerase chain reaction) test (NR: not provided) not reported, was awaiting results. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from suspected covid-19 infection, and the outcome of suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This case, involving the same patient is linked to 20220123821 (dose number in series 1). This case is associated with product quality complaint: 90000211932.; Sender's Comments: V0-20220124204- covid-19 vaccine ad26.cov2.s -Suspected clinical vaccination failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20210113; Test Name: COVID-19 PCR test; Result Unstructured Data: not reported
Aktuelle Erkrankungen: Allergy
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2040452

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WA
Alter: 17,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

No adverse event Product administered to patient of inappropriate age

Symptomtext

incorrectly administered Janssen vaccine to 17 year old. no adverse events to report

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2034119

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: -
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test

Symptomtext

COVID AFTER RECEIVING THE JANSSEN COVID-19 VACCINE; This spontaneous report received from a consumer concerned a 38 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 14-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On 12-JAN-2022, Laboratory data included: COVID-19 virus test (not provided) Positive. On an unspecified date, the patient experienced covid after receiving the janssen covid-19 vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of covid after receiving the janssen covid-19 vaccine was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220112; Test Name: COVID-19 virus test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2030935

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: FL
Alter: 22,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: -
Beginn: 03.01.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

SARS-CoV-2 test Suspected COVID-19 Vaccination failure

Symptomtext

SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 22 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration not reported, batch number: 211A21A, expiry: unknown) dose was not reported, dose number in series was 01, 01 in total was administered on 24-SEP-2021 on left arm for prophylactic vaccination. No concomitant medications were reported. On 03-JAN-2022, the patient experienced dry cough, headache, nausea, light headedness, weird taste and had suspected clinical vaccination failure. On 04-JAN-2022, Laboratory data included: coronavirus disease (COVID-19) virus test (rapid) which was positive. At the time of reporting patient just had dry cough and headache (dose number in series was 01). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from suspected covid-19 infection, and the outcome of suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with regulatory authority. This case, from the same reporter is linked to 20220112121.; Sender's Comments: V0:20220109542-covid-19 vaccine ad26.cov2.s- suspected clinical vaccination failure. This event is considered not related. The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event than the drug. Specifically: SPECIAL SITUATIONS

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20220104; Test Name: COVID-19 virus test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no known allergies.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2030927

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: PA
Alter: 40,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 10.11.2021
Beginn: 31.12.2021
Tage bis Beginn: 51,0
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID 19 INFECTION; This spontaneous report received from a patient concerned a 41 year old female. Initial information processed along with the follow up information received on 07-JAN-2022. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient had no known allergies. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1, unspecified manufacturer) (suspension for injection, route of admin and batch number were not reported, expiry: unknown) dose was not reported, 1 total administered on unspecified date in APR-2021 for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26. cov2.s (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: unknown) dose was not reported, 1 total administered on the left arm on 10-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 31-DEC-2021, the patient experienced symptoms tired, body aches and headaches (subsumed under confirmed covid-19 infection and confirmed clinical vaccination failure) (dose number in series 2). On 01-JAN-2022, patient tested positive for Covid-19. Laboratory data included: COVID-19 virus test (NR: not provided) positive. On 02-JAN-2022, Covid-19 symptoms of tiredness, body aches and headache resolved. She was not aware of being in contact of anyone who was Covid-19 positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from confirmed covid 19 infection, and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report is associated with product quality complaint number 90000210071. The suspected product quality complaint has been confirmed to be the reported allegation could not be confirmed. A manufacturing related root cause could not be identified based on the Regulatory Authority evaluation/investigation performed. .; Sender's Comments: V0- 20220104848- covid-19 vaccine ad26.cov2.s -Confirmed clinical vaccination failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220101; Test Name: COVID-19 virus test; Result Unstructured Data: positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no known allergies
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2024010

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: FL
Alter: 58,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: -
Beginn: 30.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

SARS-CoV-2 test Suspected COVID-19 Vaccination failure

Symptomtext

SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 58 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26. cov2.s (Janssen, Dose number in series 1) (suspension for injection, route of admin was not reported, batch number: 1805031, expiry: UNKNOWN) dose was not reported, 1 total, administered on 14-MAR-2021 for prophylactic vaccination. It was unknown if patient had adverse event following vaccination with covid-19 vaccine ad26.cov2.s (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (Janssen, Dose number in series 2) (suspension for injection, route of admin was not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, 1 total, administered on 16-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. The patient's son was symptomatic and tested positive on 24-DEC-2021. The patient reported exposure from son who was visiting from college. On 30-DEC-2021, the patient was tested positive for COVID-19 using the home kit test sent by JnJ. He was feeling "a little bit under the weather" and reported symptoms such as a little bit of chills, difficulty breathing, fatigue, cough, and congestion (suspected covid-19 infection and suspected clinical vaccination failure) (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from suspected covid-19 infection, and the outcome of suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000209617.; Sender's Comments: V0: 20211265893-COVID-19 VACCINE AD26.COV2.S-Suspected clinical vaccination failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20211230; Test Name: SARS-CoV-2 rapid diagnostic test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2017603

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: GA
Alter: -
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: -
Beginn: 04.01.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

COVID-19 TESTED POSITIVE; This spontaneous report received from a patient concerned a male of unspecified age. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: UNKNOWN) dose was not reported, administered on 09-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 04-JAN-2022, the patient experienced covid-19 tested positive. Laboratory data included: Body temperature (NR: not provided) 101 F, and COVID-19 rapid POC test (NR: not provided) Positive, Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from covid-19 tested positive. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Body temperature
Hospital-Tage: -
Labordaten: Test Date: 20220104; Test Name: COVID-19 rapid POC test; Result Unstructured Data: Positive; Test Date: 20220104; Test Name: Body temperature; Result Unstructured Data: 101 F; Test Date: 20220104; Test Name: COVID-19 rapid POC test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2017597

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

TESTED POSITIVE FOR COVID AFTER RECEIVING THE JANSSEN COVID 19 VACCINE; This spontaneous report received from a consumer concerned a 43 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 01-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced tested positive for covid after receiving the janssen covid 19 vaccine. Laboratory data (dates unspecified) included: COVID-19 rapid POC test (NR: not provided) Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of tested positive for covid after receiving the janssen covid 19 vaccine was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Name: COVID-19 rapid POC test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2010833

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 32,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Interchange of vaccine products

Symptomtext

Patient received Moderna vaccine for first 2 shots, received incorrect booster for 3rd shot - Janssen in error.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2010261

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

gering

Staat: WA
Alter: 16,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

No adverse event Product administered to patient of inappropriate age

Symptomtext

After reviewing the vaccine with patient and parent, both wanted jj vaccine and since he was over 250 pounds and state of emergency vaccine was given

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: none needed no illness resulted
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2010245

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

gering

Staat: WA
Alter: 17,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Product administered to patient of inappropriate age

Symptomtext

discussed vaccine with parent and patient and they wanted the jj vaccine due to almost being 18 and being over 250 pounds no sickness resulted

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2010223

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

gering

Staat: WA
Alter: 17,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Product administered to patient of inappropriate age

Symptomtext

parent and patient wanted the jj vaccine since she was about to be 18 and she was over 250 pounds and the state of emergency to get vaccinations done it was decided to do the vaccine eventhough she was 17

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1994572

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19

Symptomtext

COVID AFTER BEING VACCINATED WITH THE JANSSEN COVID 19 VACCINE; This spontaneous report received from a patient concerned a 39 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose, start therapy date were not reported for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced covid after being vaccinated with the janssen covid 19 vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of covid after being vaccinated with the janssen covid 19 vaccine was not reported. This report was non-serious. This report was associated with product quality complaint.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1991642

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: PA
Alter: 54,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: -
Beginn: 27.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

SARS-CoV-2 test Suspected COVID-19 Vaccination failure

Symptomtext

SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 54 year male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of administration not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, 1 total, administered at left arm on 05-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 25-DEC-2021, patient has been testing negative Saturday and Sunday with the rapid test since he was exposed to his wife who tested positive on Saturday 25-DEC-2021. Laboratory data included: SARS-CoV-2 rapid diagnostic test (NR: not provided) Negative. On 26-DEC-2021, Laboratory data included: SARS-CoV-2 rapid diagnostic test (NR: not provided) Negative. On 27-DEC-2021, the patient tested positive with a rapid home kit test for COVID-19 (suspected clinical vaccination failure, and suspected covid-19 infection), patient reports a little bit of joint and muscle fatigue and some tightness in chest and reports being relatively well. Laboratory data included: SARS-CoV-2 rapid diagnostic test (NR: not provided) Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from suspected covid-19 infection, and the outcome of suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20211258883-COVID-19 VACCINE AD26.COV2.S- suspected covid-19 infection. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). 20211258883-COVID-19 VACCINE AD26.COV2.S- suspected clinical vaccination failure. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20211225; Test Name: SARS-CoV-2 rapid diagnostic test; Result Unstructured Data: Negative; Test Date: 20211226; Test Name: SARS-CoV-2 rapid diagnostic test; Result Unstructured Data: Negative; Test Date: 20211227; Test Name: SARS-CoV-2 rapid diagnostic test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1988204

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 29.12.2021
Impfdatum: -
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Poor quality product administered Product storage error

Symptomtext

VIALS HAD A TEMPERATURE EXCURSION THEN ADMINISTERED TO PATIENTS; INCORRECT PRODUCT STORAGE; This spontaneous report received from a multiple patients of unspecified age, sex, race and ethnicity. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patients was previously treated with covid-19 vaccine ad26. cov2. s (unspecified manufacturer) for (suspension for injection, route of admin not reported, batch number: unknown and expiry: unknown) 1 total, dose was not reported, administered on unspecified day for prophylactic vaccination (Dose number in series 1). No known events were reported after vaccination. The patients received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A and expiry: 14-DEC-2021) 1 total, dose was not reported, administered on OCT-2021 for prophylactic vaccination (Dose number in series 2). No concomitant medications were reported. On an unspecified day in OCT-2021, vials had a temperature excursion then administered to patients and qualified for incorrect product storage. Pharmacy assistant reported that 6 unpunctured vials of Janssen COVID-19 vaccine had multiple temperature excursions between 20-OCT-2021 until 17-NOV-2021 where the minimum temperature reached was 0.6 degree Celsius and the maximum temperature reached was 9.6 degree Celsius. The excursion happened while the vials were in the fridge and the temperature readings were recorded every 5 minutes. The pharmacy checked the temperature excursion information online and found that there was no restriction in duration for storage of unpunctured vials excursion temperature range between 0 to 1 degree Celsius and also no restriction if between 9 to 10 degree Celsius so the pharmacy administered the vaccine from these vials. They administer 5 booster shots and 1 primary shot between Oct-2021 and NOV-2021 when the vials were not expired. The pharmacy assistant was calling to confirm that the temperature excursion information found online for those temperature ranges was correct and that the vials were not adversely affected. The patients who received the vaccine from these vials did not report any adverse events to the pharmacy. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vials had a temperature excursion then administered to patients and incorrect product storage was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1983845

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: AZ
Alter: 52,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: -
Beginn: 15.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE USED; This spontaneous report received from a health care professional concerned a 52 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no known allergies. The patient had not experienced any harm from the product problem (no associated adverse event). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A, expiry: 14-DEC-2021) .5 ml, administered on 15-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 15-DEC-2021, the patient experienced expired vaccine used. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine used was not reported. This report was non-serious. This case, from the same reporter is linked to 20211237771.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: The patient had no known allergies. The patient had not experienced any harm from the product problem (no associated adverse event).
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1970420

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

ADMINISTRATION OF EXPIRED VACCINE; This spontaneous report received from a health care professional concerned a 63 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin, and batch number not reported) dose was not reported,1 total, therapy start date was not reported for prophylactic vaccination. No adverse event reported post primary vaccination (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, 1 total, administered on 15-DEC-2021 into left arm for prophylactic vaccination. No concomitant medications were reported. On 15-DEC-2021, the patient experienced administration of expired vaccine (dose number in series 2) and no other adverse events reported. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of administration of expired vaccine was not reported. This report was non-serious. This case, from the same reporter is linked to 20211235069.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1970384

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

ADMINISTRATION OF EXPIRED VACCINE; This spontaneous report received from a health care professional concerned a 64 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin, and batch number not reported) dose was not reported,1 total, therapy start date was not reported for prophylactic vaccination. No adverse event reported post primary vaccination (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported,1 total, administered on 15-DEC-2021 on left arm for prophylactic vaccination. No concomitant medications were reported. On 15-DEC-2021, the patient administered expired vaccine (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administration of expired vaccine was not reported. This report was non-serious. This case, from the same reporter is linked to 20211235341.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1966630

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WA
Alter: 56,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: -
Beginn: 16.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

ADMINISTRATION OF JANSSEN COVID 19 VACCINE THAT EXPIRED BY TWO DAYS; This spontaneous report received from a health care professional concerned a 56 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 16-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 16-DEC-2021, the patient experienced administration of janssen covid 19 vaccine that expired by two days. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of administration of janssen covid 19 vaccine that expired by two days was not reported. This report was non-serious. This case, from the same reporter is linked to 20211240774.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1966629

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WA
Alter: 72,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: -
Beginn: 16.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

ADMINISTRATION OF JANSSEN COVID 19 VACCINE THAT WERE EXPIRED BY TWO DAYS; This spontaneous report received from a health care professional concerned a 72 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, administered on 16-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 16-DEC-2021, the patient experienced administration of janssen covid 19 vaccine that were expired by two days. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of administration of janssen covid 19 vaccine that were expired by two days was not reported. This report was non-serious. This case, from the same reporter is linked to 20211240943.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1961117

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: AZ
Alter: -
Geschlecht: U
Eingang: 18.12.2021
Impfdatum: -
Beginn: 15.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE USED; This spontaneous report received from a health care professional concerned multiple patients. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 15-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 15-DEC-2021, the patient experienced expired vaccine used. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine used was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1959432

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WA
Alter: 72,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

On Dec 16th our team mistakenly administered an expired vaccine to this patient. The vaccine expired on 12/14. The patient experienced no complications at the time of vaccination, nor has had any issues since. Patient and health department were notified. Manufacturer contact and advised that patient does not need to repeat vaccination at this time

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1957755

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: IN
Alter: 46,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: -
Beginn: 10.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test

Symptomtext

CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 46 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: high blood pressure, and seasonal allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, administered on 10-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 10-DEC-2021, the patient experienced confirmed covid-19 infection. On 12-DEC-2021, Laboratory data included: COVID-19 virus test (NR: not provided) Positive. Laboratory data (dates unspecified) included: COVID-19 virus test (NR: not provided) negative. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from confirmed covid-19 infection. This report was non-serious. This report was associated with a product quality complaint: 90000206767.; Sender's Comments: V0: Medical assessment comment is not required as per standard procedure as case is assessed as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20211212; Test Name: COVID-19 virus test; Result Unstructured Data: Positive; Test Name: COVID-19 virus test; Result Unstructured Data: negative
Aktuelle Erkrankungen: Blood pressure high; Seasonal allergy
Vorgeschichte: Comments: Unknown
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1955778

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WA
Alter: 78,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Product storage error

Symptomtext

Pt here to receive Janssen booster. It was given. As it was being charted, it was discovered that it was two days past its expiration date. That particular vial expired on 12/14/21 and it was given today, 12/16/21. Pt is aware. Provider in clinic also aware.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: AAA, Atherosclerosis of coronary artery, HTN, Ischemic cardiomyopathy, Peripheral vascualar occlusive disease, renal artery stenosis, SVT, migraine variant, GERD, hyperlipidemia, asthma, sleep apnea, sinus disease, CKD, renal insufficiency, dizziness
Andere Medikamente: Albuterol, Amlodipine, Vit C, ASA, famotidine, ferosul, Advair, fluticasone, furosemide, gabapentin, losartin, magnesium, meoprolol succ, mupirocin oint,, omeprazole, zofran, miralax, crestor, tamsulosin, vanlafxine
Allergien: clopidogrel
Vorherige Impfungen: -

VAERS 1954091

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 27,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: -
Beginn: 28.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Underdose

Symptomtext

RECEIVED A HALF DOSE FOR THEIR BOOSTER DOSE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 27 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient was previously received with covid-19 vaccine ad26. cov2..s (unspecified manufacturer) (suspension for injection, route of admin not reported, batch number: unknown expiry: UNKNOWN) dose was not reported, 1 in total, (dose number in series: 1) for prophylactic vaccination The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported batch number: 1822809 ,211A21A expiry: UNKNOWN) 0.25 ml, 1 in total, administered on 28-NOV-2021 for prophylactic vaccination. (dose number in series: 2) No concomitant medications were reported. On 28-NOV-2021, the patient experienced received a half dose for their booster dose (coded as Vaccine under dose) On 28-NOV-2021, the patient experienced off label use (both events dose number in series: 2). The reporter stated that something was printed and was disseminated which said to administer 0.25ml. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the received a half dose for their booster dose and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211202250, 20211202193, 20211201082, 20211200752, 20211200994, 20211201450, 20211201351, 20211201046, 20211202469, 20211202515, 20211200675, 20211201168, 20211201179, 20211201228, 20211201304 20211201392, 20211201443, 20211201963, 20211202161, 20211202199, 20211200717, 20211200723, 20211200769 20211201362, 20211202207, 20211202246, 20211202371 and 20211202379.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1954089

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 26,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: -
Beginn: 28.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Underdose

Symptomtext

RECEIVED A HALF DOSE FOR THEIR BOOSTER DOSE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 26 year old male of unspecified race and ethnicity. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: unknown expiry: unknown) dose was not reported, 1 total, administered on unspecified dated for prophylactic vaccination (manufacturer not otherwise specified, dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number was either or 211A21A (batch/lot number also reported by HCP as: 1822809) expiry: UNKNOWN) 0.25 ml (milliliter), frequency one total, administered on 28-NOV-2021 for prophylactic vaccination (dose number in series 2). No concomitant medications were reported. On 28-NOV-2021, the patient received a half dose for their booster dose (captured as: Vaccine under dose) and off label use (dose number in series 2). The reporter stated that something was printed and was disseminated which said to administer 0.25ml. As reported in source document, HCP (health care provider) was transferred to MICC (unknown acronym definition) for further assistance. HCP (from public health dept) stated that there were 33 patients who received half doses (0.25ml) for their booster or 3rd dose a few days ago. Most of them were patients from Texas. HCP stated that something was printed and disseminated that said to administered .25ml. HCP is not sure where that information came from. Stated it was over the holidays so people could have thought that info changed and staff was just not made aware. HCP did not think it has been reported yet through VAERS. HCP stated at the time of report that the vendor will file the report with VAERS, the the public health department. HCP stated that they figure it out after the event because they could not figure out how so many doses were given. They were looking for a discrepancy in the number of vials perhaps, but then realized that half doses were given. HCP consented to being contacted, but that she may not be the best person to contact. If she had an alternate contact she will provide it to whomever reaches out to her. HCP stated that Spartan is the vendor. They teamed up together to gather information and they may have called to report these events as well, so be mindful of possible duplicate reports. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the received a half dose for their booster dose and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211202469, 20211202515, 20211200675, 20211201168, 20211201179, 20211201228, 20211201228, 20211201304, 20211201351, 20211201362, 20211201392, 20211201443, 20211201450, 20211201963, 20211202161, 20211202199, 20211200717, 20211200723, 20211200769, 20211200994, 20211201286, 20211202207, 20211202246, 20211202250, 20211202371, 20211202379, 20211201046, 20211204104, 20211220152, 20211220146, 20211220262, 20211220250, 20211220145, 20211220619 and 20211220155.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1950443

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 28,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: -
Beginn: 27.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Underdose

Symptomtext

RECEIVED HALF DOSE FOR THEIR BOOSTER DOSE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 28 year old male of unspecified race and ethnic origin. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: unknown, expiry: unknown) dose was not reported, 1 total, administered on unspecified date for prophylactic vaccination. (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number was 211A21A expiry: unknown) 0.25 ml, 1 total, administered on 27-NOV-2021 for prophylactic vaccination (Dose number in series is 2). No concomitant medications were reported. On 27-NOV-2021, the patient received half dose for their booster dose (coded as vaccine under dose and off label use). As described by reporter, HCP (health care provider) (from public health dept) stated that there were 33 patients who received half doses (0.25ml (milliliter) for their booster or 3rd dose a few days ago. Most of them were patients from Texas. HCP stated that something was printed and disseminated that said to administer .25ml. HCP was not sure where that information came from. Stated it was over the holidays so people could have thought that info changed and staff was just not made aware. HCP did not think it had been reported yet through VAERS. HCP thought that the vendor will file the report with VAERS, not public health department. HCP stated that they figured it out after the event because they could not figure out how so many doses were given. They were looking for a discrepancy in the number of vials perhaps, but then realized that half doses were given. HCP consented to being contacted, but stated that she may not be the best person to contact. If she had an alternate contact she would provide it to whomever reached out to her. The reporter went on to report that HCP stated that Spartan is the vendor. At the time of the discussion they were both teaming up together to gather information and they may have called to report these events as well, so HCP warned to be mindful of possible duplicate reports.(Dose number in series is 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the received half dose for their booster dose and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211202250, 20211201046, 20211201082, 20211201228, 20211201168, 20211200752, 20211200717, 20211201351, 20211200994, 20211201450, 20211202199, 20211202469, 20211201286, 20211204104, 20211202379, 20211201179, 20211201443, 20211220146, 20211220262, 20211220250, 20211220145, 20211220619, 20211220129, 20211219871 and 20211220152.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1950440

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 28,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: -
Beginn: 27.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Underdose

Symptomtext

RECEIVED HALF DOSE FOR THEIR BOOSTER DOSE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 28 year old female of unspecified race and ethnic origin. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26.cov2.s (manufacturer not specified) (suspension for injection, route of admin not reported, batch number: unknown, expiry: unknown) dose was not reported, 1 total, administered on unspecified date for prophylactic vaccination. (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number 211A21A expiry: unknown) dose was not reported, 1 total, administered on 27-NOV-2021 for prophylactic vaccination. (Dose number in series 2). No concomitant medications were reported. On 27-NOV-2021, the patient experienced received half dose for their booster dose (vaccine underdose) and had off label use (dose series 2). HCP (from public health department) stated that there were 33 patients who received half doses (0.25ml) for their booster or 3rd dose. Most of them were patients from unknown. HCP stated that something was printed and disseminated that said to administer .25ml. HCP was not sure where that information came from. Stated it was over the holidays so people could have thought that info changed and staff was just not made aware. HCP stated that they figured it out after the event because they could not figure out how so many doses were given. They were looking for a discrepancy in the number of vials perhaps, but then realized that half doses were given. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the received half dose for their booster dose and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211202250, 20211201046, 20211202193, 20211201228, 20211201168, 20211200752, 20211201351, 20211200994, 20211201450, 20211202199, 20211202469, 20211201362, 20211204104, 20211202379, 20211201179, 20211202515, 20211200675, 20211201179, 20211201304, 20211201392, 20211201963, 20211202161, 20211200717, 20211200723, 20211200769, 20211202207, 20211202246, 20211202371, 20211220152, 20211220146, 20211220262, 20211220250, 20211220145, 20211219871, 20211219926 and 20211220155.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1942126

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 28.09.2021
Beginn: 06.12.2021
Tage bis Beginn: 69,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Abortion spontaneous Exposure during pregnancy Ultrasound foetal abnormal

Symptomtext

Miscarriage at 6 weeks gestational age. No prior medical history. Had 1 prior healthy live birth. No high risk behaviors such as smoking, drinking, recreational drugs use.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abortion spontaneous
Hospital-Tage: -
Labordaten: Confirmed by ultrasound
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prenatal
Allergien: None
Vorherige Impfungen: -

VAERS 1941717

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 55,0
Geschlecht: M
Eingang: 11.12.2021
Impfdatum: -
Beginn: 13.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Overdose

Symptomtext

RECEIVED 2.5ML OF THE JANSSEN COVID-19 VACCINE; This spontaneous report received from a health care professional concerned a 55 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) 2.5 ml, administered on 13-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-NOV-2021, the patient experienced received 2.5ml of the janssen covid-19 vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of received 2.5ml of the janssen covid-19 vaccine was not reported. This report was non-serious. This case, from the same reporter is linked to 20211220948, 20211221158, 20211221439, 20211221529, 20211219731, 20211219686, 20211220537, 20211220233 and 20211219807.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Overdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1941715

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 30,0
Geschlecht: M
Eingang: 11.12.2021
Impfdatum: -
Beginn: 14.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

RECEIVED 2.5ML OF THE JANSSEN COVID-19 VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 30 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: 14-DEC-2021) 2.5 ml, administered on 14-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-NOV-2021, the patient experienced received 2.5ml of the janssen covid-19 vaccine. On 14-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the received 2.5ml of the janssen covid-19 vaccine and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211219731, 20211219686, 20211220537, 20211220233, 20211219807, 20211220948, 20211221158 and 20211221439.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1941710

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 35,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: -
Beginn: 14.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

RECEIVED ONLY 2.5ML OF THE JANSSEN COVID-19 VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 35 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) 2.5 ml, administered on 14-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-NOV-2021, the patient experienced received only 2.5ml of the janssen covid-19 vaccine. On 14-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the received only 2.5ml of the janssen covid-19 vaccine and off label use was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1941709

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 37,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: -
Beginn: 13.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Overdose

Symptomtext

OVERDOSE (RECEIVED 2.5ML OF THE JANSSEN COVID-19 VACCINE); This spontaneous report received from a health care professional concerned a 37 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) 2.5 ml, administered on 13-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-NOV-2021, the patient experienced overdose (received 2.5ml of the janssen covid-19 vaccine). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of overdose (received 2.5ml of the janssen covid-19 vaccine) was not reported. This report was non-serious. This case, from the same reporter is linked to 20211219681, 20211219953, 20211220301, 20211220527, 20211220178, 20211220177, 20211220552, 20211220619, 20211220146, 20211220754, 20211220129, 20211220764, 20211219701, 20211219871, 20211219926, 20211219714, 20211219701, 20211220145 and 20211220928.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Overdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1941706

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 79,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: -
Beginn: 14.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

OVERDOSE (RECEIVED 2.5 ML OF THE JANSSEN COVID-19 VACCINE); OFF LABEL USE; This spontaneous report received from a health care professional concerned a 79 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) 2.5 ml, administered on 14-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-NOV-2021, the patient experienced overdose (received 2.5 ml of the janssen covid-19 vaccine). On 14-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the overdose (received 2.5 ml of the janssen covid-19 vaccine) and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211220262, 20211220206, 20211220527, 20211220178, 20211220537, 20211220552, 20211220155, 20211220697, 20211220754, 20211219731, 20211219701, 20211219807, 20211219714, 20211220233, 20211220460, 20211220216 and 20211220177.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1941704

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 47,0
Geschlecht: M
Eingang: 11.12.2021
Impfdatum: -
Beginn: 14.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Incorrect dose administered Off label use

Symptomtext

OFF LABEL USE; RECEIVED ONLY 2.5ML OF THE JANSSEN COVID-19 VACCINE; This spontaneous report received from a health care professional concerned a 47 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) 2.5 ml, administered on 14-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-NOV-2021, the patient experienced received only 2.5ml of the janssen covid-19 vaccine. On an unspecified date, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of received only 2.5ml of the janssen covid-19 vaccine and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211220916, 20211219681, 20211220301, 20211220527, 20211220697 and 20211220928.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938988

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 31,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: -
Beginn: 14.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

RECEIVED 2.5ML OF THE JANSSEN COVID-19 VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 31 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: 14-DEC-2021) 2.5 ml, administered on 14-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-NOV-2021, the patient experienced received 2.5ml of the janssen covid-19 vaccine. On 14-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the received 2.5ml of the janssen covid-19 vaccine and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211219386, 20211219731, 20211219686, 20211220537, 20211220233, 20211219807, 20211220948 and 20211221158.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938986

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 38,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: -
Beginn: 14.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

ADMINISTERED 2.5ML OF THE VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 38 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) 2.5 ml,, administered on 14-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-NOV-2021, the patient experienced administered 2.5ml of the vaccine. On 14-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administered 2.5ml of the vaccine and off label use was not reported. This report was non-serious. This case, involving the same patient is linked to 20211201168. This case, from the same reporter is linked to 20211220129, 20211220146, 20211220152, 20211202199, 20211202193, 20211202161, 20211201963, 20211201450, 20211201443, 20211201392, 20211201351, 20211201304, 20211201286, 20211201179, 20211201168, 20211200994, 20211201082, 20211200723, 20211200717, 20211200675, 20211165041, 20211202371, 20211202250, 20211202246, 20211202207, 20211202193, 20211201963, 20211201228, 20211201046, 20211200769, 20211200752, 20211200723, 20211165041, 20211219871 and 20211220155.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938985

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 32,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: -
Beginn: 07.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

RECEIVED ONLY 2.5ML OF THE JANSSEN COVID-19 VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 32 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine (suspension for injection, route of admin not reported, batch number: 211A21A and expiry: 14-DEC-2021) 2.5 ml, administered on 07-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 07-NOV-2021, the patient experienced received only 2.5ml of the janssen covid-19 vaccine. On 07-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine was not applicable. The outcome of the received only 2.5ml of the janssen covid-19 vaccine and off label use was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938878

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 67,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: -
Beginn: 31.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

OVERDOSE (RECEIVED 2.5ML OF THE JANSSEN COVID-19 VACCINE); OFF LABEL USE; This spontaneous report received from a health care professional concerned a 67 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) 2.5 ml, administered on 31-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 31-OCT-2021, the patient experienced overdose (received 2.5ml of the janssen covid-19 vaccine). On 31-OCT-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the overdose (received 2.5ml of the janssen covid-19 vaccine) and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211220178, 20211220537, 20211220177, 20211220552, 20211220155, 20211220619, 20211220152, 20211220697, 20211220146, 20211220754, 20211220764, 20211219953, 20211220916, 20211220948, 20211219714, 20211219701, 20211219871, 20211219686, 20211219681, 20211219926 and 20211219731.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938875

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 21,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: -
Beginn: 14.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

ADMINISTERED 2.5ML OF THE VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 21 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A and expiry: 14-DEC-2021) 2.5 ml, administered on 14-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-NOV-2021, the patient experienced administered 2.5ml of the vaccine. On 14-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administered 2.5ml of the vaccine and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211220129, 20211220146, 20211220152, 20211219681, 20211165041, 20211165041, 20211200723, 20211200752, 20211200769, 20211201046, 20211201228, 20211201963, 20211202193, 20211202207, 20211202246, 20211202250, 20211202371, 20211165041, 20211200675, 20211200717, 20211200723, 20211201082, 20211200994, 20211201168, 20211201179, 20211201286, 20211201304, 20211201351, 20211201392, 20211201443, 20211201450, 20211201963, 20211202161, 20211202193, 20211202199, 20211219871 and 20211220301.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938874

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 52,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: -
Beginn: 31.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

ADMINISTERED 2.5ML OF THE VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 52 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 211A21A expiry: 14-DEC-2021) 2.5 ml, administered on 31-OCT-2020 for prophylactic vaccination. No concomitant medications were reported. On 31-OCT-2021, the patient experienced administered 2.5ml of the vaccine. On 31-OCT-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administered 2.5ml of the vaccine and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211220129, 20211220146, 20211220916, 20211220152, 20211219926, 20211219871, 20211220301, 20211220145, 20211220527, 20211220250, 20211165041, 20211200723, 20211200752, 20211201046, 20211201228, 20211201963, 20211201450, 20211201443, 20211201392, 20211201351, 20211201304, 20211201286, 20211201179, 20211201168, 20211200994, 20211201082, 20211200723, 20211200717, 20211219681 and 20211200675.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938873

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: -
Beginn: 14.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

ADMINISTERED 2.5ML OF THE VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 54 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A and expiry: 14-DEC-2021) 2.5 ml, administered on 14-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-NOV-2021, the patient experienced administered 2.5ml of the vaccine. On 14-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administered 2.5ml of the vaccine and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211220129, 20211220619, 20211220155, 20211220145, 20211220250, 20211220262, 20211220916, 20211165041, 20211200723, 20211200752, 20211201046, 20211201228, 20211201963, 20211202193, 20211202207, 20211202246, 20211202250, 20211202371, 20211165041, 20211202199, 20211202193, 20211202161, 20211201963, 20211201450, 20211201443, 20211201392, 20211201351, 20211201304, 20211201286, 20211201179, 20211201168, 20211200994, 20211201082, 20211200723, 20211200717, 20211219681, 20211200675, 20211220527, 20211220697 and 20211220928.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938393

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 52,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: -
Beginn: 13.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

RECEIVED ONLY 2.5ML OF THE JANSSEN COVID-19 VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 52 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) 2.5 ml, administered on 13-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-NOV-2021, the patient experienced received only 2.5ml of the janssen covid-19 vaccine. On 13-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the received only 2.5ml of the janssen covid-19 vaccine and off label use was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938386

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 30,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: -
Beginn: 14.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

RECEIVED ONLY 2.5 ML OF THE JANSSEN COVID-19 VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 30 year old female. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 14-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-NOV-2021, the patient experienced received only 2.5 ml of the janssen covid-19 vaccine. On 14-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the received only 2.5ml of the janssen covid-19 vaccine and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211219686, 20211219701, 20211219807 and 20211219871.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938385

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 22,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: -
Beginn: 13.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

RECEIVING 2.5ML OF THE JANSSEN COVID-19 VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 22 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: 14-DEC-2021) 2.5 ml, administered on 13-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-NOV-2021, the patient experienced receiving 2.5ml of the janssen covid-19 vaccine. On 13-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the receiving 2.5ml of the janssen covid-19 vaccine and off label use was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938384

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 63,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: -
Beginn: 14.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

RECEIVED 2.5ML OF THE JANSSEN COVID-19 VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 63 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) 2.5 ml, administered on 14-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-NOV-2021, the patient experienced received 2.5ml of the janssen covid-19 vaccine. On 14-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine was not applicable. The outcome of the received 2.5ml of the janssen covid-19 vaccine and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211219681, 20211219953, 20211220301, 20211220460, 20211220206, 20211220178, 20211220537, 20211220177, 20211220552, 20211220155, 20211220619, 20211220697, 20211220146, 20211220754, 20211220129, 20211220764, 20211220916, 20211220948, 20211219714, 20211219701, 20211219686, 20211219731 and 20211219807. .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938381

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 19,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: -
Beginn: 14.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

RECEIVING ONLY 2.5ML OF THE JANSSEN COVID-19 VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 19 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: 14-DEC-2021) 2.5 ml, administered on 14-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-NOV-2021, the patient experienced receiving 2.5ml of the janssen covid-19 vaccine. On 14-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the receiving 2.5ml of the janssen covid-19 vaccine and off label use was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938376

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: AZ
Alter: 27,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: -
Beginn: 13.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

ADMINISTERED 2.5ML OF THE VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 27 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 211A21A expiry: 14-DEC-2021) 2.5 ml, administered on 13-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-NOV-2021, the patient experienced administered 2.5ml of the vaccine. On 13-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administered 2.5ml of the vaccine and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211220129, 20211220916, 20211200769, 20211200675, 20211200717, 20211201082, 20211200994, 20211201168, 20211201179, 20211201286, 20211201304, 20211201351, 20211201392, 20211201443, 20211201450, 20211202161, 20211202199, 20211220262, 20211220250, 20211219871, 20211219926, 20211219681, 20211219871, 20211202207, 20211220619, 20211219926, 20211220145, 20211220155, 20211202246, 20211202250 and 20211202371.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938369

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: OK
Alter: 52,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: -
Beginn: 31.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

RECEIVED 2.5ML OF THE JANSSEN COVID-19 VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 52 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 31-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 31-OCT-2021, the patient experienced received 2.5ml of the janssen covid-19 vaccine. On 31-OCT-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the received 2.5ml of the janssen covid-19 vaccine and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211219386, 20211219686 and 20211219807.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938364

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 22,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: -
Beginn: 13.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Off label use Overdose

Symptomtext

RECEIVED 2.5ML OF THE JANSSEN COVID-19 VACCINE; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 22 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) 2.5 ml, administered on 13-NOV-2021 for prophylactic vaccination (Dose series number : 1). No concomitant medications were reported. On 13-NOV-2021, the patient experienced received 2.5ml of the janssen covid-19 vaccine. On 13-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the received 2.5ml of the janssen covid-19 vaccine and off label use was not reported. This report was non-serious. This case, from the same reporter is linked to 20211219807, 20211219686 and 20211219731.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Off label use
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932646

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 27,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932637

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 26,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Incorrect dose administered

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932633

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 30,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932628

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 31,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932622

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 59,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932619

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 57,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932611

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 59,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932506

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 48,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932498

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 27,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932391

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 25,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Incorrect dose administered

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929544

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929541

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 52,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929528

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 59,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929518

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 52,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929328

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 38,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929313

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 47,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Incorrect dose administered

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929291

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 34,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929273

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 29,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929255

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 30,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929228

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929201

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 63,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Vaccine dosage administered at half dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1914220

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: OH
Alter: 40,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 08.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Blood test Glycosylated haemoglobin increased Pollakiuria Thirst Vision blurred Weight decreased

Symptomtext

Increase thirst Frequent urination Rapid weight loss of 30 lbs within 1 1/2 months Blurry vision Elevated A1C

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: Blood work 11/22/21 And 11/29/21
Aktuelle Erkrankungen: None
Vorgeschichte: High BP high cholesterol
Andere Medikamente: Lisinopril Rosuvastatin ca Pantoprazole na
Allergien: Bee stings
Vorherige Impfungen: -

VAERS 1913418

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: MT
Alter: 92,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 19.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19

Symptomtext

diagnosed and hospitalized with COVID while fully vaccinated

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1892829

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Dyspepsia Throat tightness

Symptomtext

throat tightness and heartburn

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspepsia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: unknown
Andere Medikamente: escitalopram, tretinoin, spironolactone, liothyronine, levothyroxine
Allergien: gluten, morphine, soy
Vorherige Impfungen: Pfizer Comirnaty, lot ER 8732

VAERS 1880919

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

gering

Staat: CO
Alter: 51,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Extra dose administered Interchange of vaccine products

Symptomtext

Patient received first dose of Pfizer on 0729/21 and the second dose was received on 08/19/2021. This Registered nurse was giving patients booster shots per their request. I went through all the paper work and had separated the piles based on when they last received their dose. This patients paper work ended up in the pile with the patients who needed a booster. This patient received a 3rd shot on 11/18/2021 of a johnson and johnson vaccine. Prior to the shot this RN went over the fact sheet with this patient and he was unsure of when and what injection he received as it was at the hospital. No adverse reactions have been reported by this patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: None as of now. This Patient has just received the dose on 11/18/2021
Aktuelle Erkrankungen: None reported per patient
Vorgeschichte: none reported per patient
Andere Medikamente: cogentin, prozac, lisinopril, lithium ER, zyprexa, seroquel
Allergien: Haldol
Vorherige Impfungen: -

VAERS 1879213

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TN
Alter: -
Geschlecht: U
Eingang: 18.11.2021
Impfdatum: -
Beginn: 15.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Poor quality product administered

Symptomtext

VACCINE FROM OPENED VIAL WAS ADMINISTERED PAST THE SIX HOUR USE BY TIME FOR OPENED VIALS; This spontaneous report received from a pharmacist concerned a patient of unspecified age and sex. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered on 15-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 15-NOV-2021, the patient experienced vaccine from opened vial was administered past the six hour use by time for opened vials. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of vaccine from opened vial was administered past the six hour use by time for opened vials was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1877069

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Interchange of vaccine products

Symptomtext

Patient presented to the outreach booth at the downtown transfer center reporting a desire to be vaccinated for COVID. Reported he had not had COVID vaccine yet, answered no to the screening questions. Mobile harm reduction outreach event did not have a way to check records prior to vaccination. When his record was pulled up later at the office to document his vaccine, it showed a first dose of Pfizer given 30 days prior.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: None reported
Allergien: None reported
Vorherige Impfungen: -

VAERS 1873094

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TN
Alter: 56,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 15.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered No adverse event

Symptomtext

No adverse effects reported. The vial was expired when given to patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1870051

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: MT
Alter: 17,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Product administered to patient of inappropriate age

Symptomtext

No treatment needed at this time, reporting that patient is 17 years of age and not 18. She was given a EUA. I did inform her of other vaccines due to risks of blood clotting. She said, "she would prefer Johnson & Johnson, because they were going out of state and did not have enough time for the other vaccines." Since this event, we have implemented safety measures and a more through verification process.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: Denies
Vorgeschichte: Uknown
Andere Medikamente: Unknown
Allergien: Denies allergies to latex, medications, food or vaccines, eggs, bovine protein, gelatin, gentamicin, polymyxin, neomycin, phenol, yeast, or thimerosal, latex, polyethylene glycol
Vorherige Impfungen: -

VAERS 1868281

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 22,0
Geschlecht: M
Eingang: 14.11.2021
Impfdatum: 14.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

A puncture vial from 11/13/2021 was not disposed of at the end of the clinic. On 11/14/2021 the RN in charge of drawing up the vaccine used the punctured vial that had been open more than 6 hours to provide a vaccine to a patient. After the dose was administered it was discovered she had used the expired punctured vial. The vial was immediately disposed of. We consulted the CDC's "COVID-19 Vaccine Administration Errors and Deviations" document and were directed to "Contact the manufacturer for information on the stability of the vaccine. If the manufacturer does not have data to support the stability of the vaccine, repeat the dose immediately (no minimum interval).*" After consulting the Janssen website and the Janssen "FACT SHEET FOR HEALTHCARE PROVIDERS ADMINISTERING VACCINE (VACCINATION PROVIDERS)" we were unable to find any information on the stability of punctured vials after 6 hours. We are going to contact the patient to inform them of the error and repeat the dose as per the CDC's recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1866961

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: OH
Alter: -
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: -
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Increased tendency to bruise Lymphopenia Skin discolouration Thrombocytopenia Urine analysis

Symptomtext

LOW LEVEL OF WHITE BLOOD CELLS; WBC IN URINE; RBC IN URINE; THROMBOCYTOPENIA; LYMPHOCYTOPENIA; MARKS AND PURPERA UNDER THE SKIN; GET EASILY BRUISED; This spontaneous report received from a patient concerned a 69-year-old female. The patient's height, and weight were not reported. The patient's past medical history included: back fusion, and concurrent conditions included: lung damage due to pollution and inhaling snow ash, arthritis, and genetic abnormality. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, 01 total administered to left arm on 07-OCT-2021 for prophylactic vaccination. Concomitant medications included Methyl folate (calcium levomefolate) for genetic abnormality, Vitamin B12 amino (cyanocobalamin), Vitamin B6 (pyridoxine hydrochloride), and Vitamin B1 (thiamine) for unknown indication. The patient was taking unspecified injection subcutaneously for arthritis. None of her concomitant conditions or her medication interfered or contraindicated from taking the vaccine. After receiving vaccine, the patient did not experience any side effect not even a pain in site of injection. She had only normal pain for receiving an injection. On 01-NOV-2021, she went to do some pre-operation blood and urine test as she was scheduled to get a morphine pump implanted in mid-December due to her previous condition of back fusion. The blood test came back with low level of White Blood Cells (WBC) (absolute white blood cell count that was low), thrombocytopenia and lymphocytopenia. The urine test came back with WBC and Red Blood Cells (RBC) in urine but no blood in urine as per caller. Her doctor repeated the urine test on 03-NOV-2021 or 04-NOV-2021 and it was the same. The blood test was re-done on 04-NOV-2021 and came back with the same result. Both her surgeon and her doctor recommended her to urgently see a hematologist. Her surgery was put on hold until she saw her hematologist. She never had anything close to this. Her doctor was against her taking any vaccine and wanted her to wait for nova vax. But she took vaccine due to her lung condition (lung damage due to pollution and inhaling snow ash to the point that she lost her voice). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the thrombocytopenia, lymphocytopenia, marks and purpera under the skin, low level of white blood cells, WBC in urine, RBC in urine and get easily bruised was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20211118705-covid-19 vaccine ad26.cov2.s-thrombocytopenia. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: Test Date: 20211101; Test Name: Blood test; Result Unstructured Data: Low white blood cells; Test Date: 202111; Test Name: Urine analysis; Result Unstructured Data: WBC, RBC in urine; Test Date: 20211101; Test Name: Urine analysis; Result Unstructured Data: WBC, RBC in urine; Test Date: 20211104; Test Name: Blood test; Result Unstructured Data: Low white blood cell
Aktuelle Erkrankungen: Arthritis; Congenital anomaly; Lung disorder (Patient lost voice)
Vorgeschichte: Medical History/Concurrent Conditions: Spinal fusion (scheduled to get a morphine pump implanted in mid December)
Andere Medikamente: VITAMIN B1 [THIAMINE]; VITAMIN B6; VITAMIN B12 AMINO; METHYL FOLATE
Allergien: -
Vorherige Impfungen: -

VAERS 1860119

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: MT
Alter: 52,0
Geschlecht: M
Eingang: 11.11.2021
Impfdatum: -
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Poor quality product administered Product storage error

Symptomtext

VACCINE VIAL WAS PUNCTURED ON 04-NOV-21 AT 19:15, THEN ADMINISTERED ON 05-NOV-21 AT 11:28 AM; PUNCTURED VACCINE STORED IN THE REFRIGERATOR OVERNIGHT; This spontaneous report received from a pharmacist concerned a 52 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 05-NOV-2021 11:28 for prophylactic vaccination. No concomitant medications were reported. On NOV-2021, the patient experienced punctured vaccine stored in the refrigerator overnight. On 05-NOV-2021, the patient experienced vaccine vial was punctured on 04-nov-21 at 19:15, then administered on 05-nov-21 at 11:28 am. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the punctured vaccine stored in the refrigerator overnight and vaccine vial was punctured on 04-nov-21 at 19:15, then administered on 05-nov-21 at 11:28 am was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1858378

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: MT
Alter: 52,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Error of expired Janssen dose given. Janssen vial opened 11/4 at 1915. Doses are normally discarded when clinic closes for the night but this time it was not. Vial was left in refrigerator. Patient received Jannsen 0.5 mL IM 11/5 at 1128 (~10 hours expired). Dose was stored in refrigerator. Spoke with Janssen who stated they did not have any additional information on the stability and to consider the vaccine expired. They said to defer to provider to make a clinical decision. Janssen case file (redacted). Same day care manager called patient to relay that does was expired and physician recommended a repeat dose (ID provider Dr.). Patient lives far away and did not want to come back for a second dose. No active side effects as of phone call to patient on 11/10 per manager

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1857980

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 57,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Induration Swelling face

Symptomtext

Patient states that approximately 2 hours after receiving his Janssen booster vaccine for Covid 19, it was noticed that his left cheek was slightly swollen and area firm to touch.. states he has a mild numbness of left cheek. with uneven smile. No other symptoms. States symptoms are decreasng 12 hours later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypoaesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: None known
Vorherige Impfungen: -

VAERS 1853154

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WA
Alter: -
Geschlecht: U
Eingang: 09.11.2021
Impfdatum: -
Beginn: 05.11.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Poor quality product administered Product storage error

Symptomtext

ADMINISTRATION OF JANSSEN COVID-19 VACCINE AFTER BEING PUNCTURED FOR MORE THAN 6HRS; VIAL OF VACCINE PUNCTURED OUTSIDE OF THE 6 HOUR TIME HOUR; This spontaneous report received from a health care professional concerned a patient of unspecified age and sex. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 05-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 05-NOV-2021, the patient experienced administration of janssen covid-19 vaccine after being punctured for more than 6 hrs. On 05-NOV-2021, the patient experienced vial of vaccine punctured outside of the 6 hour time hour. The action taken with covid-19 vaccine was not applicable. The outcome of the administration of janssen covid-19 vaccine after being punctured for more than 6hrs and vial of vaccine punctured outside of the 6 hour time hour was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1850657

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CO
Alter: 16,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Product administered to patient of inappropriate age

Symptomtext

Patient is 16 years old, and therefore should have received the Pfizer COVID vaccine, rather than the Janssen COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1849141

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: UT
Alter: 58,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 06.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blindness unilateral Photopsia Retinal detachment Ultrasound eye abnormal Vision blurred Visual impairment Vitreous floaters

Symptomtext

Oct 11th, right eye had floaters. Oct 12th, right eye flashes. Oct 14th, right eye floaters, flashes, and cloudiness. Oct 16th, right eye small constant black spot in the lower left hand corner of the visual spectrum. Oct 17th, right eye went completely blind. Went to the ER, and they performed an ultrasound, this showed that there had been a retinal detachment. Oct 18th, saw an ophthalmologist and the retina detachment was confirmed. Later that day, I saw a Retinal Specialist, the Retinal Detachment was confirmed along with there being enough of a tear that fluid had enter into the macular part of the eye. Surgery has been scheduled.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blindness unilateral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: High Blood Pressure, Atrial Fibrillation
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1844333

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WA
Alter: 57,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 30.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Skin discolouration

Symptomtext

Patient suddenly developed numbness in one hand and his fingers became white below the knuckles then while on the phone with the pharmacy asking advise about the event his other hand became numb and began to turn white. Patient was advised to seek prompt medical attention.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypoaesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1832888

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WI
Alter: 17,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

No adverse event Product administered to patient of inappropriate age

Symptomtext

At our COVID-19 vaccine clinic 10/20/21 this individual put on their consent form that they were 18 but their birthday that they also put on the form would put them at age 17. They requested J&J and were given it because their consent form said they were 18. The clinic was busy and the DOB age was not caught until the dose was being put into the database. We are unsure at this point if they deliberately ?posed? as 18 just to get J&J. Parent was informed after the fact. There was no adverse reaction for this individual that we know of due to this administered dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1832341

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: MN
Alter: 63,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 14.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Postmenopausal haemorrhage Vaginal haemorrhage

Symptomtext

Beginning about 4:00 p.m., 8 days post-jab, vaginal bleeding began. There was approximately 1 Tbsp. bright red blood with small clots noted, which lessened, eventually to minor pink tinged discharge lasting 48-72 hours. No cramping or discomfort was noted. I am 63 years old and post-menopauasal. I have not menstruated for almost 10 years. I have no history of gynocological issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Postmenopausal haemorrhage
Hospital-Tage: -
Labordaten: None. I notified my primary physician and was instructed to continue to monitor and report any changes.
Aktuelle Erkrankungen: None. Hx of bilateral knee replacement July 2021
Vorgeschichte: Arthritis
Andere Medikamente: Multi-vit., B-Complex, Vit. D3, Glucosamine-Condroitin
Allergien: None known
Vorherige Impfungen: -

VAERS 1831614

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CO
Alter: 29,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 06.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Menstruation delayed Pregnancy test negative

Symptomtext

Getting the vaccine threw off my very predictable menstrual cycle. My period is 5 days late and I am not pregnant. As someone who is trying to conceive, this is devastating.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Menstruation delayed
Hospital-Tage: -
Labordaten: Negative pregnancy tests every day from 10-26 through 10-30
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 1830702

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WA
Alter: 37,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: -
Beginn: 28.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Poor quality product administered

Symptomtext

VACCINE ADMINISTERED AFTER THE 30 MINUTES OUTSIDE OF EXPIRY TIME (VIAL PUNCTURED AT 9 AM AND ADMINISTERED AT 3.30 PM); This spontaneous report received from a health care professional concerned a 37 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, administered on 28-OCT-2021 15:30 for prophylactic vaccination. No concomitant medications were reported. On 28-OCT-2021, the patient experienced vaccine administered after the 30 minutes outside of expiry time (vial punctured at 9 am and administered at 3.30 pm). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of vaccine administered after the 30 minutes outside of expiry time (vial punctured at 9 am and administered at 3.30 pm) was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1827173

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: KY
Alter: 48,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: -
Beginn: 26.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Poor quality product administered Product storage error

Symptomtext

PUNCTURED VIAL OF THE VACCINE WAS ADMINISTERED EXCEEDED TIME FRAME BY 1 ONE HOUR OUTSIDE OF THE 6 HOUR TIME PERIOD; VIAL OF VACCINE WAS PUNCTURED OUTSIDE OF THE 6 HOUR TIME PERIOD; This spontaneous report received from a health care professional concerned a 48 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered on 26-OCT-2021 15:05 for prophylactic vaccination. No concomitant medications were reported. On 26-OCT-2021, the patient experienced punctured vial of the vaccine was administered exceeded time frame by 1 one hour outside of the 6 hour time period. On 26-OCT-2021, the patient experienced vial of vaccine was punctured outside of the 6 hour time period. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the punctured vial of the vaccine was administered exceeded time frame by 1 one hour outside of the 6 hour time period and vial of vaccine was punctured outside of the 6 hour time period was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1820430

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: -
Beginn: 25.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Poor quality product administered Product storage error

Symptomtext

INCORRECT PRODUCT STORAGE; ADMINISTRATION OF VACCINE FROM PUNCTURED VIAL LEFT OVERNIGHT (OVER 6 HOURS); This spontaneous report received from a pharmacist concerned a 61 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 25-OCT-2021 11:14 for prophylactic vaccination. No concomitant medications were reported. On 25-OCT-2021, the patient experienced administration of vaccine from punctured vial left overnight (over 6 hours). On an unspecified date, the patient experienced incorrect product storage. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administration of vaccine from punctured vial left overnight (over 6 hours) and incorrect product storage was not reported. This report was non-serious. This case, from the same reporter is linked to 20211049878.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1820427

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: -
Beginn: 25.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Poor quality product administered

Symptomtext

VIAL WAS PUNCTURED AND LEFT OVERNIGHT (OVER 6 HOURS); This spontaneous report received from a pharmacist concerned a 57 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 25-OCT-2021 11:40 for prophylactic vaccination. No concomitant medications were reported. On 25-OCT-2021, the patient experienced vial was punctured and left overnight (over 6 hours). The action taken with covid-19 vaccine was not applicable. The outcome of vial was punctured and left overnight (over 6 hours) was not reported. This report was non-serious. This case, from the same reporter is linked to 20211050252.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1818241

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 05.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Amenorrhoea Menstrual disorder

Symptomtext

Prior to taking the Covid-19 Janssen vaccination, I have had normal menstrual cycles since menstruation began at age 11. After receiving the shot on 10/5/ 21 menstrual cycle was expected between 10/13/2021 - 10/18/2021 and did no come. Cycle still has yet to come, even though all typical symptoms revolving around cycle have occurred (menstrual cramps, face break out, etc). There is no pregnancy, medications, or use of birth control to affect this change.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Amenorrhoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1815219

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

gering

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Product storage error

Symptomtext

expired vaccine was injected

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: na
Vorgeschichte: na
Andere Medikamente: na
Allergien: na
Vorherige Impfungen: -

VAERS 1815201

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

gering

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Product storage error

Symptomtext

the vaccine was expired ,was over 6 hours and was left at room temperature

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: na
Allergien: na
Vorherige Impfungen: -

VAERS 1808751

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WI
Alter: 38,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Extra dose administered Interchange of vaccine products No adverse event

Symptomtext

Client received Covid19 vaccine, Janssen at pop up clinic. Client reported he had not yet received any Covid19 vaccines. Dose was administered and when data entry occurrred later that day, staff realized that client had previously received both J&J and Pfizer. Client notified. No adverse reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1804794

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: MO
Alter: 23,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Underdose

Symptomtext

After administering the vaccine into the patient's arm, the needle retracted back into the syringe forcefully and the vaccine squirted out back toward the nurse giving the dose. After the nurse looked at the syringe there was still liquid inside the syringe and leaking out the bottom of the syringe. It appeared that the vaccine did not enter the patient's arm. After discussing what happened with the patient, the patient decided to receive a second dose. After administering the second dose the patient stated that she could feel the vaccine enter her arm where as she did not feel it with the first shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: unknown
Allergien: -
Vorherige Impfungen: -

VAERS 1804764

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WI
Alter: 17,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Product administered to patient of inappropriate age

Symptomtext

1.Client signed consent form herself even though under 18. 2. Client received Janssen vaccine even though under 18.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1801588

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 14,0
Geschlecht: M
Eingang: 20.10.2021
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

No adverse event Product administered to patient of inappropriate age

Symptomtext

No adverse events was noted. No treatment was provided. Client remained in the observation area for 15 minutes and left with parent. No signs of acute distress was observed or noted. The client left the observation area at 1257.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: No medical test or laboratory results related to the adverse event exist to my knowledge.
Aktuelle Erkrankungen: There were no ilnesses reported at the time of vaccination or up to one month prior as reported by client and parent.
Vorgeschichte: There were no chronic or long-standing health conditions as reported by the client or parent.
Andere Medikamente: No prescriptions, over-the-counter medications, dietary supplements, or herbal remedies were being taken at the time of vaccination as reported by the client and parent.
Allergien: There were no allergies to medications, food, or other products that were reported by the client or parent.
Vorherige Impfungen: -

VAERS 1785786

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: MO
Alter: 23,0
Geschlecht: M
Eingang: 19.10.2021
Impfdatum: -
Beginn: 13.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Poor quality product administered Product storage error

Symptomtext

STORAGE OF VACCINE OUTSIDE OF THE RECOMMENDED STORAGE CONDITIONS; ADMINISTRATION OF VACCINE STORED OUTSIDE OF THE RECOMMENDED STORAGE; This spontaneous report received from a health care professional concerned a 23 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient had no known drug allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered on 13-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-OCT-2021, the patient experienced administration of vaccine stored outside of the recommended storage. On an unspecified date, the patient experienced storage of vaccine outside of the recommended storage conditions. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administration of vaccine stored outside of the recommended storage and storage of vaccine outside of the recommended storage conditions was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no known drug allergies
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1789934

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 53,0
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: unbekannt

Interchange of vaccine products

Symptomtext

Patient had made an appointment for a dose of Janssen. Patient received the dose of Janssen, but system would only allow Pfizer vaccine to be selected. On further investigation, system showed that PT received a dose of Pfizer vaccine on 8/7/21. On the paper screening form that we used, he attested that he had not received a previous dose of any COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1789897

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: NE
Alter: 68,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: -
Beginn: 08.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Tinnitus

Symptomtext

TINNITUS/INCREASE AND PERSISTENT RINGING IN THE EARS; This spontaneous report received from a patient concerned a 68 year old female. The patient's height, and weight were not reported. The patient's past medical history included: tinnitus, and supraventricular tachycardia. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) dose was not reported, administered on 08-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-OCT-2021, the patient experienced tinnitus/increase and persistent ringing in the ears. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from tinnitus/increase and persistent ringing in the ears. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Supraventricular tachycardia; Tinnitus
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1780456

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WY
Alter: 16,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Product administered to patient of inappropriate age

Symptomtext

16-year-old received a J & J by mistake.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1779346

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: ND
Alter: 51,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Interchange of vaccine products

Symptomtext

Johnson & Johnson vile was pulled and given instead of Moderna

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: NA
Vorherige Impfungen: -

VAERS 1777004

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WI
Alter: 39,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Extra dose administered Interchange of vaccine products

Symptomtext

Pt was given a Johnson and Johnson instead of Moderna for 2nd dose Covid Vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1776622

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 11.10.2021
Impfdatum: 24.09.2021
Beginn: 24.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest discomfort Interchange of vaccine products Throat irritation

Symptomtext

throat burning and chest tightness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest discomfort
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ADD, Raynaud disease, migraines, anxiety, concussion syndrome
Andere Medikamente: methylphenidate, bupropion
Allergien: nkda
Vorherige Impfungen: Pfizer COVID-19 vaccine, given 1/31/21, facial swelling and redness

VAERS 1775672

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 14,0
Geschlecht: F
Eingang: 10.10.2021
Impfdatum: 10.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

No adverse event Product administered to patient of inappropriate age

Symptomtext

No reaction. Patient was observed for approximately 15 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1775188

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 30,0
Geschlecht: M
Eingang: 09.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Interchange of vaccine products

Symptomtext

Patient presented to the vaccination site on 10/05/21. The client notified RN that he received a single dose of the (AstraZeneca) COVID vaccine on (5/29/21). RN submitted a medical consult via text message requesting to proceed with the COVID vaccine Janssen. Per CDC guidance, approval to proceed with COVID vaccine Janssen was obtained via text message. Client received COVID vaccine Janssen Lot# 211A21A on 10/05/2021. The client did not report any symptoms during the observation period. The client left the vaccination site at 1401.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1773415

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: ND
Alter: 19,0
Geschlecht: M
Eingang: 09.10.2021
Impfdatum: -
Beginn: 07.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Poor quality product administered

Symptomtext

POTENTIALLY EXPIRED VACCINE ADMINISTERED (VIAL WAS OPENED ON 06-OCT-2021 AT 9 AM AND VACCINE ADMINISTERED ON 07-OCT-2021 AT AROUND 12:30 TO 1 PM); This spontaneous report received from a pharmacist concerned a 19 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered on 07-OCT-2021 for prophylactic vaccination. No concomitant medications were reported. On 07-OCT-2021, the patient experienced potentially expired vaccine administered (vial was opened on 06-oct-2021 at 9 am and vaccine administered on 07-oct-2021 at around 12:30 to 1 pm). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of potentially expired vaccine administered (vial was opened on 06-oct-2021 at 9 am and vaccine administered on 07-oct-2021 at around 12:30 to 1 pm) was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1772121

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 21,0
Geschlecht: M
Eingang: 08.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hyperhidrosis Musculoskeletal stiffness Pallor Tension Unresponsive to stimuli

Symptomtext

10 seconds after vaccination, pt's body tensed, he became pale and unresponsive. Arms and body became flexed and stiff. He was placed on floor, 911 called, Ammonia inhalant used with immediate response. VS stable, pt continued to be responsive. Skin was pale and diaphoretic. Denied headache, chest pain, SOB, nausea. No rash noted on skin, lungs clear, no wheezing. Pt improved, took sips of water and ate a snack. Tolerated well, no emesis. Medics arrived, assessed pt, offered transport to hospital but pt refused. Medics provided instruction to seek medical attention if symptoms return or worsen. Pt monitored for 30 minutes post event, no further symptoms. Ambulated without assist, steady gait to car.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hyperhidrosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Pt stated he has fainted with a previous vaccine. Of note, is that his two siblings also fainted. One had received Pfizer, and o

VAERS 1768949

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 29.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia

Symptomtext

complained of left arm numbness that occurred the day after vaccination that has spread to the fingers, which has continued to this date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypoaesthesia
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Benadryl
Allergien: Latex & to flu shots
Vorherige Impfungen: she stated that she has allergic reactions to the flu shot

VAERS 1768754

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: KS
Alter: 26,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

No adverse event

Symptomtext

Patient stated that she suffers severe anaphylactic response to multiple antibiotics. Food items as listed previously. Patient denies citrus sensitivity. Patient taken to EMS room at 12:25 PM. Lead RN notified. Benadryl 25 mg po given at 12:20 PM. Patient sat on cot with bottled water while injection of J&J vaccine administered at 12:30 without incident. Patient was closely monitored for adverse symptoms. Patient denies these symptoms at this time. 12:40 PM, patient is texting on phone without any problems breathing or otherwise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: -
Allergien: Sulfa, Keflex, Azithromycin, Clindamycin, Amoxicillin, penicillin, Z-Pack. Almonds, tree nuts, beef, milk, nuts, cheese, dairy products, red dye
Vorherige Impfungen: -

VAERS 1768723

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: KS
Alter: 56,0
Geschlecht: M
Eingang: 07.10.2021
Impfdatum: 25.09.2021
Beginn: 25.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Unevaluable event

Symptomtext

Reviewed history with patients. Getting shot because of job. Worried since he had reacted to allergy shot in the past with anaphylaxis and Penicillin with a rash. Pre-shot, Two Benadryl tablets 25mg each given orally pre-vaccine. No Issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: Gave two Benadryl 25mg orally pre vaccine. No issues.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Penicillin
Vorherige Impfungen: Allergy shots 5 years prior

VAERS 1759658

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WA
Alter: 35,0
Geschlecht: F
Eingang: 04.10.2021
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Interchange of vaccine products

Symptomtext

We gave patient Janssen on 10/1/21 because patient said she had not receive any Covid vaccine before. Insurance rejection showed that patient received Pfizer vaccine on 09/27/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1758377

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 69,0
Geschlecht: M
Eingang: 04.10.2021
Impfdatum: -
Beginn: 27.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Inappropriate schedule of product administration Off label use

Symptomtext

OFF LABEL USE; INAPPROPRIATE SCHEDULE OF VACCINE ADMINISTRATION; This spontaneous report received from a health care professional concerned a 69 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered on 27-SEP-2021, and dose was not reported, administered on 15-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 27-SEP-2021, the patient experienced off label use. On 27-SEP-2021, the patient experienced inappropriate schedule of vaccine administration. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the off label use and inappropriate schedule of vaccine administration was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1755747

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CO
Alter: 49,0
Geschlecht: M
Eingang: 02.10.2021
Impfdatum: -
Beginn: 30.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Poor quality product administered

Symptomtext

RECEIVED EXPIRED DOSE OF VACCINE; This spontaneous report received from a pharmacist concerned a 49 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 211A21A expiry: 14-DEC-2021) dose was not reported, administered on 30-SEP-2021 for prophylactic vaccination. No concomitant medications were reported. On 30-SEP-2021, the patient experienced received expired dose of vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of received expired dose of vaccine was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1754207

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: LA
Alter: 33,0
Geschlecht: M
Eingang: 01.10.2021
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: nein

Extra dose administered Interchange of vaccine products

Symptomtext

Patient arrived, stated he wished to receive his first COVID Vaccine. Patient completed Registration paperwork, denied being previously vaccinated. Patient received Janssen vaccine as per protocol. When entering vaccine into state database, it was discovered that patient had previously received a total of three Pfizer vaccines {02/05/2021, 02/25/2021, & 09/01/2021}. Patient was unable to be reached by phone as he did not give a phone contact on registration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1754138

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: WA
Alter: 43,0
Geschlecht: F
Eingang: 01.10.2021
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

Interchange of vaccine products

Symptomtext

Patient received more than one type of COVID-19 vaccine. They received one dose of Moderna 4/14/2021, then one dose of Janssen 9/30/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 1753343

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

gering

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 01.10.2021
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: unbekannt Erholt: unbekannt

Extra dose administered Interchange of vaccine products

Symptomtext

Pt came into pharmacy and said he needed a covid shot. RPh and pt spoke about each one and together they decided on Janssen. No problems with administration and no side effects afterwards. Once we logged dose into the system, we saw pt had moderna 1st dose 1/15/21, 2nd dose 2/12/21 and a 3rd dose 3/5/21. Pt had no knowledge of these shots, no white card and these were not given at our pharmacy. Notified pt and daughter of extra dose. Pt has memory problems per daughter, but is still allowed to drive and appears to be cognitively intact when we spoke to him. No adrs reported. Pt more then adequately vaccinated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1750254

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 54,0
Geschlecht: M
Eingang: 30.09.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
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 Interchange of vaccine products No adverse event

Symptomtext

Janssen vaccine given after pt. received first dose of Astrazeneca in another country. Primary care physician requested second dose of COVID -19 be given in this country. No adverse reactions noted in observation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1747515

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211a21a

gering

Staat: MN
Alter: 55,0
Geschlecht: F
Eingang: 30.09.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Sleep disorder Tinnitus

Symptomtext

Ringing in ears awoke me from sound sleep within 12 hours from injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sleep disorder
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal allergies depression edema after back injury
Andere Medikamente: Effexor, lasix, xyzal ,
Allergien: Benadryl macrodantin
Vorherige Impfungen: -

VAERS 1745402

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TX
Alter: 59,0
Geschlecht: F
Eingang: 29.09.2021
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: ja

Anxiety Hyperventilation

Symptomtext

Anxiety, hyperventilating

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anxiety
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Thyroid condition (did not specify)
Andere Medikamente: Unknown Rx for Thyroid
Allergien: Eggs, Fish, beets
Vorherige Impfungen: -

VAERS 1741238

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 24.09.2021
Beginn: 24.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

No adverse event Product storage error

Symptomtext

Pt was given Janssen 45mins after the expiration time. Pt and clinic lead were notified immediately. Pt reported no adverse effects after 30mins observation. Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Sjogren's disease, Migraines Heart disease
Andere Medikamente: Medications: APAP 500mg Q 6hrs PRN, Ibuprofen 800mg TID PRN, Ondansetron ODT 4mg TID PRN
Allergien: Allergies: Shellfish (Rash), sumatriptan (neck stiffness), Lactose (abdominal disorder)
Vorherige Impfungen: -

VAERS 1739955

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CO
Alter: -
Geschlecht: M
Eingang: 28.09.2021
Impfdatum: -
Beginn: 22.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Poor quality product administered

Symptomtext

COVID 19 VACCINE GIVEN 6 HOURS AND 23 MINUTES AFTER THE FIRST PUNCTURE OF THE VIAL; This spontaneous report received from a health care professional concerned a male of unspecified age. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, and expiry: 14-DEC-2021) dose was not reported, administered on 22-SEP-2021 15:13 for prophylactic vaccination. No concomitant medications were reported. On 22-SEP-2021, the patient experienced covid 19 vaccine given 6 hours and 23 minutes after the first puncture of the vial. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of covid 19 vaccine given 6 hours and 23 minutes after the first puncture of the vial was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1737102

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: TN
Alter: 58,0
Geschlecht: F
Eingang: 27.09.2021
Impfdatum: 24.09.2021
Beginn: 24.09.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Extra dose administered

Symptomtext

Patient presented to drive-through requesting a Janssen COVID vaccine. She replied yes when asked if she was getting her first COVID vaccine today, and answered "no" to "Have you ever received a COVID-19 vaccine?" on her paperwork. After assessment, she received her vaccine without incident, and subsequently waited 15 minutes with no problems. It was discovered while entering data in database that the patient had received a dose of Janssen vaccine on 04/08/2021. The patient was contacted by RN, who verified that she did receive the vaccine on that date. She also stated that the vaccination provider recommended an additional dose of Janssen in six months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1734740

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CA
Alter: 38,0
Geschlecht: M
Eingang: 25.09.2021
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: ja

Interchange of vaccine products No adverse event

Symptomtext

On Saturday, September 25, 2021 client came to vaccination POD for a Covid-19 Janssen dose. Client stated to ancillary staff during check-in process that he was vaccinated with Covid-19 vaccine 7 months ago in February, without proof of vaccination. At this time Covid-19 vaccine is not a vaccine approved. Elevated to Medical team & Vaccine Operations Lead and approved client to get the Janssen vaccine as it has been more than 28 days since receiving the one dose of non-FDA-authorized Covid-19 vaccine. Client has no history of allergies or previous adverse reactions to other vaccines. Client was to be a 15 minute wait in the Observation Area. Client received his Covid-19 Janssen (LOT #: 211A21A) at approximately 10:32 AM in his left arm. Client experienced no adverse reaction while waiting in Observation Area and left vaccination site with a steady gait at approximately 10:50 AM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: none
Vorherige Impfungen: -

VAERS 1730189

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CO
Alter: -
Geschlecht: M
Eingang: 24.09.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Poor quality product administered Product storage error

Symptomtext

EXPIRED DOSE ADMINISTERED; INCORRECT PRODUCT STORAGE; This spontaneous report received from a health care professional concerned a male of unspecified age. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: 14-DEC-2021) dose, start therapy date were not reported for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced expired dose administered, and incorrect product storage. The action taken with covid-19 vaccine was not applicable. The outcome of the incorrect product storage and expired dose administered was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Poor quality product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1730185

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: MT
Alter: 39,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: -
Beginn: 22.09.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Exposure during pregnancy

Symptomtext

VACCINE EXPOSURE DURING PREGNANCY; This spontaneous pregnancy report received from a patient concerned a 39 year old female. The patient's weight was 247 pounds, and height was 60 inches. The patient's concurrent conditions included: gestational diabetes, and other pre-existing medical conditions included: The patient was pregnant at the time of reporting. The patient experienced drug allergy when treated with dimeticone, and titanium dioxide. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211A21A, expiry: UNKNOWN) dose was not reported, administered on 22-SEP-2021 for prophylactic vaccination. Concomitant medications included insulin aspart for gestational diabetes, and insulin human for gestational diabetes. On 22-SEP-2021, the patient experienced vaccine exposure during pregnancy. The date of the patient's last menstrual period was 01-APR-2021 and expected delivery date was 09-JAN-2022. The pregnancy was continuing. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of vaccine exposure during pregnancy was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Exposure during pregnancy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Gestational diabetes (It is requiring long acting and fast acting insulin, both given in the AM and at bed time (Novolin and Novolog).)
Vorgeschichte: Comments: The patient was pregnant at the time of reporting.
Andere Medikamente: NOVOLOG; NOVOLIN
Allergien: -
Vorherige Impfungen: -

VAERS 1727376

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: CO
Alter: 39,0
Geschlecht: M
Eingang: 23.09.2021
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered No adverse event

Symptomtext

Patient received one dose of Janssen from a vial that was opened for 6 hours and 23 minutes causing the dose to be expired by 23 minutes at the time the patient received it. Vaccine vial and dose was maintained in cooler between 2 degrees and 8 degrees Celsius prior administration. Patient experienced no adverse reactions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1727084

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 211A21A

gering

Staat: NE
Alter: 37,0
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

Symptomtext

Patient stated they had not been previously vaccinated for Covid-19 and attested to that on their consent form. After giving the shot and patient left, we were attempting to bill it to insurance and it rejected with a code of "second dose in series not covered" I called and asked him if he for sure had not gotten a covid vaccine in the past and he stated he had not. I said I would get back to him. I then looked him up on the Immunization Registry and he has gotten 3 Pfizer doses and 1 Moderna vaccine at other locations. I have tried to called him to discuss with him the fact that he should not be seeking further vaccination and has exceeded the recommended doses for covid-19 and he has not returned my call as of 9/23/21 at 5:15 pm. His covid vaccination history is as follows: Pfizer 1 of 3 3/18/21 Pfizer 2 of 3 4/8/21 Pfizer 3 of 3 8/20/21 Moderna 1 of 1 9/18/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -