- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 14.06.2023
- Impfdatum
- 06.10.2021
- Beginn
- 16.03.2023
- Tage bis Beginn
- 526,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Anaemia
Angiogram pulmonary abnormal
Bladder outlet obstruction
Blood creatinine decreased
Blood lactic acid increased
Blood potassium decreased
Blood sodium decreased
Brain natriuretic peptide increased
C-reactive protein increased
COVID-19
COVID-19 pneumonia
Cardiopulmonary exercise test abnormal
Chronic obstructive pulmonary disease
Condition aggravated
Haemoglobin decreased
Haemophilus infection
Symptomtext
Patient is a 68 y.o. male patient of Physician No with history of CLL, COPD and tobacco abuse who presented to the ED on 3/16 who presented with shortness of breath and malaise for the past week. On arrival to the hospital, patient was hypoxic at 82% requiring 6 L nasal cannula. Other vital signs include temperature 100.1, heart rate 113 and respiratory rate of 22. Lab work was significant for sodium of 130, potassium 3.2, creatinine 2.33, CRP 110, BNP 1400, lactic acid 2.3, white blood cell count of 30, hemoglobin 11.2, platelets 50 and positive COVID test. CTA of the chest was performed and negative for pulmonary embolism. Also showed prominent patchy areas of groundglass and alveolar opacities in the lower lobes bilaterally. Background changes of COPD are also present. Patient was admitted to the hospital for hypoxia and suspected COVID/bacterial pneumonia. He received judicious fluids in the setting of COVID with progressive improvement in his renal function to baseline. Oncology was consulted and hydroxyurea continued during his stay. Broad spectrum abx started on admission with reduction to ceftriaxone due to neg mrsa swab and positive strep antigen. Also, sputum came back positive for H. Influ which was also sensitive to rocephin. Oxygen require was de-escalated to 2L NC but could not be titrated further. Ultimately, he was hemodynamically stable and discharged home on 2L NC on 3/10. Six minute walk test was performed demonstrating need for home oxygen due to COPD and COVID pneumonia. A script for Omnicef was sent to his pharmacy to complete a 10 day treatment. A script for decadron 6 mg daily for 5 days and albuterol was also sent to his pharmacy. He was instructed to wear his oxygen until re-evaluation by a PCP for which info was provided to establish. Discharge diagnosis Sepsis (tachypnea, tachycardia and pna) Acute hypoxic respiratory failure COVID Pneumonia H. Influenza Pneumonia Acute COPD exacerbation Concern for Pulm HTN, on CTA Acute Kidney Injury, resolved Chronic Bladder Outlet Obstruction, per note Hypokalemia Hyponatremia Elevated Lactic Acid MPD Anemia and thrombocytopenia, due to above Chronic Splenomegaly Hx of Gout Severe Protein Calorie Malnutrition
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 10.04.2023
- Impfdatum
- 27.10.2021
- Beginn
- 24.02.2022
- Tage bis Beginn
- 120,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Respiratory failure
Symptomtext
J96.21 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 2/24/2022 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 24.03.2023
- Impfdatum
- 28.07.2022
- Beginn
- 15.03.2023
- Tage bis Beginn
- 230,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Acute respiratory failure
Aortic stenosis
Barrett's oesophagus
Bile duct stone
Biliary dilatation
Biliary sphincterotomy
Blood potassium decreased
COVID-19
Cholecystectomy
Cholelithotomy
Computerised tomogram abdomen abnormal
Echocardiogram abnormal
Encephalopathy
Endoscopic retrograde cholangiopancreatography
Endotracheal intubation
Gallbladder disorder
Hiatus hernia
Symptomtext
Discharge summary: "Brief Summary of Hospital Stay: patient is a 74 YO female a past medical history of hypertension, hyperlipidemia, who presented to the emergency department with acute onset of nausea, vomiting, and RUQ abdominal pain shortly after meal. On arrival, the patient was hemodynamically stable but she was found to have elevated LFTs with cholestatic pattern as well as potassium 2.6. CT abdomen and pelvis was obtained which showed gallbladder and cystic duct distention, mild intrahepatic and extrahepatic biliary dilatation, radiographic findings suggestive of choledocholithiasis. Gastroenterology was consulted who recommended ERCP. Potassium was replaced. The patient initially underwent EGD given limited anesthesia availability, which was negative for Zenker's diverticulum, but did show esophageal mucosa consistent with short-segment Barrett's esophagus as well as a large hiatal hernia, otherwise unrevealing. Patient then underwent ERCP on 3/17/2023 with Dr., where biliary sphincterotomy was performed, the common bile duct was dilated, the biliary tree was swept, and choledocholithiasis was visualized and removed. Patient tolerated the procedure well. General surgery was consulted for cholecystectomy evaluation given her presentation. She underwent robotic assisted laparoscopic cholecystectomy on 3/18/2023 with another Dr. which she tolerated without immediate complicatinon. In the interim, she was receiving maintenance IV fluids. She initially tolerated the surgery well. However, postoperatively on 3/18, she began exhibiting acute encephalopathy and respiratory distress, becoming acutely hypoxic. Attempt was made to place her on BiPAP, however she acutely developed nausea and vomiting. Given her respiratory distress and aspiration risk, ICU was consulted and the patient was intubated for airway protection. The patient was diuresed and started on antibiotics given concern for aspiration pneumonia. She would improvement in her oxygen requirements and was able to be extubated on 3/19 without postextubation complication. She was transferred to floor status. Antibiotics were discontinued given low suspicion for aspiration pneumonia. Suspect that her acute respiratory decompensation was due to volume overload in setting of perioperative IV fluids and is supported chest imaging and physical exam. Echo was obtained which showed EF 50% and mild aortic stenosis and mild-moderate MR. Diuresis was continued, after which the patient demonstrated improvement in her oxygen requirements and respiratory effort, being able to wean down to room air this admission. She had resolution of her abdominal pain in her liver function testing had normalized, she otherwise remained hemodynamically stable. Patient will be discharged home with PRN Lasix to treat volume overload with close PCP follow-up. Patient will follow-up with General surgery. She was discharged home in good condition."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 7,0
- Labordaten
- COVID PCR positive test on 3/18/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 09.12.2022
- Impfdatum
- 25.08.2021
- Beginn
- 05.12.2022
- Tage bis Beginn
- 467,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
COVID-19 pneumonia
Metabolic encephalopathy
Pneumonia bacterial
SARS-CoV-2 test positive
Sepsis
Superinfection
Symptomtext
Patient received Moderna COVID vaccine on 3/3/21, 3/31/21, and 8/25/21. On 12/5/22, patient admitted to our inpatient facility (med/surg unit) with COVID-19 pneumonia, superimposed bacterial PNA, acute hypoxic respiratory failure, severe sepsis, acute metabolic encephalopathy, and AKI. As of today (12/9/22), patient is still admitted in the med/surg unit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- COVID status positive 12/5/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- SNF resident with history of CAD s/p stenting, HFrEF (35-39%), DM2, CKD, HTN, hx of TIA, lung and laryngeal SCC with metastasis, and GI bleed secondary to his stomach angiodysplasia
- Andere Medikamente
- albuterol inh, aspirin ec 81mg, atorvastatin, bisacodyl supp, clopidogrel, fentanyl patch, furosemide, guaifenesin, norco 5/235mg, insulin glargine, lactulose, metoprolol er, ondansetron, pantoprazole, polyethylene glycol, sennosides, sodiu
- Allergien
- oxycodone
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 29.09.2022
- Impfdatum
- 23.03.2021
- Beginn
- 24.09.2022
- Tage bis Beginn
- 550,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cardiac arrest
SARS-CoV-2 test positive
Symptomtext
Pt with history of MS who presented to hospital with witnessed cardiac arrest. Per family pt had tested positive for COVID a few days prior.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 27.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram pulmonary abnormal
Cardiac disorder
Computerised tomogram thorax abnormal
Deep vein thrombosis
Echocardiogram abnormal
Muscle strain
Pulmonary embolism
Ultrasound Doppler abnormal
Symptomtext
Acute pulmonary embolism - submassive - with large DVT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 5,0
- Labordaten
- CTA chest, duplex ultrasound of the legs, echocardiography all confirming DVT/PE and Right heart strain
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- ckd, gerd, hld, hypoparathyroidism
- Andere Medikamente
- Aspirin 81, Clobetasol ointment, vitorin, gabapentin norco, synthroid, lisinopril, montelukast, melatonin, miralax
- Allergien
- codeine, cyclobenazprine, diazepam, bees
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 22.07.2021
- Beginn
- 31.08.2021
- Tage bis Beginn
- 40,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Cardiac discomfort
Chest discomfort
Chills
Cough
Diarrhoea
Dizziness
Dyspnoea
Fatigue
Hallucination
Headache
Muscle spasms
Myalgia
Nausea
Oropharyngeal pain
Pain
Presyncope
Respiratory tract congestion
Symptomtext
Headache (throbbing/horrendous) Chills Sore throat Cough Shortness of breath Tightness in chest around heart Fatigue Hallucinations Dizziness Feel like I?m going to pass out Muscle & body aches Muscle Spasms Joint Pain Congestion Runny nose Nausea Diarrhea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- 08/31/21 AND 09/07/21 VISITED THE DOCTOR BECAUSE OF ADVERSE REACTIONS TO COVID INJECTIONS.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- ESCITALOPRAM 0.5mg
- Allergien
- CODIENE SULFA DILAUDID PCN
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 19.08.2021
- Beginn
- 07.10.2021
- Tage bis Beginn
- 49,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Bell's palsy
Computerised tomogram head
Facial paralysis
Full blood count
Metabolic function test
Symptomtext
Reported to the emergency room 10/7/2021 with several hours of right facial droop. Diagnosed with Bell's palsy. Treated with Prednisone and Valtrex. Seen in the office 10/13/21 with near 100% complete resolution of symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- CT head 10/7/21 normal CBC and CMP10/7/21 normal
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypothyroid, hyperlipidemia, seizure disorder, interstitial cystitis, GERD, migraines
- Andere Medikamente
- Aspirin, Elavil, Calcium carbonate, Zetia, levothyroxine, melatonin, magnesium, Protonix, Probiotic, Zanaflex, Effexor, Verapamil
- Allergien
- Bactrim
- Vorherige Impfungen
- -
- Staat
- ND
- 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 / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Electrocardiogram normal
Hyperhidrosis
Loss of consciousness
Pallor
Pulse absent
Snoring
Symptomtext
Client given moderna vaccine at 1038 AM 10/4/21 at flu/covid clinic - only covid vaccine given - at 1044 AM clients co worker informed CCHD staff that client passed out as he was noted to snore - CCHD staff noted client to be very pale, diaphoretic - client shared with CCHD staff that he was having a hard time breathing - CCHD staff nurse instructed other CCHD staff to call 911 - CCHD staff nurse got ice packs and placed in back of clients neck and on arm, staff nurse also ammonia smelling salts, cool cloth placed on clients forehead, and client provided with water and small amounts of trail mix - client verbal and answered questions when asked, however, noted to be quiet - ambulance staff arrived and clients vitals at 76/54 left arm, O2 at 96% RA, radial pulse not palpable per EMT, however, pulse on pulse ox at 46 - ambulance took client to ED for evaluation/treatment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Per ED, PA - EKG normal - no labs available at time of this report -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COVID on 4/10/21 with no treatment
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 02.10.2021
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Anaphylactic reaction
Condition aggravated
Disorientation
Fatigue
Fibromyalgia
Hypersensitivity
Muscle spasms
Pain
Tachycardia
Throat irritation
Tremor
Symptomtext
Severe allergic reaction, anaphylaxis, throat itching, tachycardia, trembling, stomach pain. Treated immediately with epinephrine and Benadryl. Several hours later, a severe fibromyalgia flare occurred, with muscle spasms, extreme pain over entire body, exhaustion, and disorientation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Fibromyalgia, hypoglycemia (non diabetic)
- Andere Medikamente
- None
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- 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: ja
Erholt: nein
Syncope
Symptomtext
Patient received his first dose of Moderna vaccine and was sitting down during the 15 minute post vaccine observation when he fell off the chair and fainted. Patient was unconscious for less than a minute. Once he recovered patient denied having any medical conditions or previous episodes of fainting after vaccines. Patient's blood pressure was taken (112/70) and 911 was called. Patient was transported to the hospital for further assessment by the first responders at around 5pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- BP 112/70.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- trees, pollen, grass
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 29.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Syncope
Symptomtext
the second dose was accidentally administered 18 days after the 1st dose, instead of 28 days. patient's grand daughter stated that she fainted 2 times after receiving the dose earlier than recommended.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 23.09.2021
- Impfdatum
- 02.09.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Chest X-ray
Chills
Decreased appetite
Diplopia
Ear discomfort
Electrocardiogram
Fatigue
Full blood count
Incontinence
Lipase
Loss of consciousness
Malaise
Metabolic function test
Pyrexia
Syncope
Troponin I
Urine analysis
Symptomtext
Pt had syncopal episode on 9/4/21. Got up early in AM to use restroom and get drink. Passed out at the kitchen sink. Spent about 3.5 hours on the ground. She believes she was in and out of conciousness at that time. Was found laying in emesis, stool, urine. Had diarrhea x3 throughout the night. Was feeling ill starting the night before with chills, subjective fever, fatigue. Had her first diarrhea episode that night. These symptoms started 1.5 days after her 2nd covid vaccine (Moderna). She was taken by EMS to the ER. Workup in ER included labs, CXR and EKG. She was treated with fluids and zofran and discharged to home. She had double vision until yesterday. This primarily occured with turning head quickly. Takes some time before eyes focus. Clicking/pressure in ears, poor appetite. Overall she feels that she has improved. No headache, N/V, diarrhea, N/V.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Hospital ER 9/4/2021- EKG, CXR, UA, CBC, BMP, Troponin I, Hepatic function panel, Lipase.
- Aktuelle Erkrankungen
- Had brief episode of weakness, runny nose, cough, nausea, diarrhea, and muscle aches after her 1st dose of Moderna covid vaccine 3 weeks prior. Symptoms resolved prior to 2nd vaccine on 9/2/21
- Vorgeschichte
- hyperlipidemia, insomnia, osteoporosis, hypertension, GERD.
- Andere Medikamente
- Alendronate, Aller-tec, Hydroxyzine, Metoprolol, Omeprazole, Raloxifene, Simvastatin
- Allergien
- Benzonatate (rash), Heparin (rash) , Influenza vaccine (diarrhea, vomiting, myalgia, fever), Macrobid (diarrhea, vomiting), Sulfa (rash)
- Vorherige Impfungen
- Influenza vaccine. Unknown date/brand/age. Patient reported hx of diarrhea, vomiting, muscle aches and fever following vaccine.
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 13.09.2021
- Impfdatum
- 13.09.2021
- Beginn
- 13.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Dizziness
Nausea
Syncope
Symptomtext
vasovagal syncope. Occurred shortly after vaccine administration. Patient was faint, nauseous, and in a cold sweat for about 15 minutes after receiving the shot. Supplied water to the patient as requested. Patient recovered after 15 minutes and was fine with no remaining symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none applicable
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none known
- Vorherige Impfungen
- vasovagal syncope as well, with MMR vaccine and moderna dose one. patient still age 26 when receiving those vaccines
- Staat
- PA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 12.09.2021
- Impfdatum
- 11.09.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Fall
Head injury
Hyperhidrosis
Loss of consciousness
Nausea
Symptomtext
Following vaccination, the patient was seated. After a few minutes they approached the pharmacy counter asking to use the bathroom as they felt nauseous, and was visibly sweating, red in color. They seemingly lost consciousness, fell forward into the plastic divider, and then backwards onto the store floor, possibly hitting their head. Pharmacist alerted the pharmacy intern to call 911, and entered the store floor to assist the patient, who had quickly regained consciousness and sat themselves up. They were offered water, after which point they reported starting to feel better, and was able to make it back into a chair on their own power until paramedics arrived, and the pharmacist relayed the details of the adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Paramedics took vital signs including blood pressure and blood sugar, and a patient medical history. It seems the patient refused to be transported to the hospital and left the pharmacy on their own accord.
- Aktuelle Erkrankungen
- No Known
- Vorgeschichte
- No Known
- Andere Medikamente
- N/a
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 10.09.2021
- Impfdatum
- 10.09.2021
- Beginn
- 10.09.2021
- 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 after she stood up to wait for her mother to get her vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 03.09.2021
- Impfdatum
- 10.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Bell's palsy
Facial paralysis
Hypoaesthesia
Paraesthesia
Symptomtext
Numbness and tingling in the left lower and upper cheek area by 8/12/2021. By mid-day on 8/16/2021 the left side of the mouth/lips were drooping and there was no elasticity in the muscles on the left side of the face. For example: I could pinch the skin on the left cheek and the skin would stay pinched- it would not go back into place unless I smoothed it down. Likewise I could also push the left lip over and it would ruffle- and stay in that position until I manually moved it back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- I saw the doctor mid morning on 8/17/2021 and was diagnosed with a mild Bells Palsy. Doctor prescribed an anti-viral.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- none- ever.
- Allergien
- slight sensitivity to soy products.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 30.08.2021
- Impfdatum
- 30.08.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Nervousness
Syncope
Thirst
Symptomtext
Approximately 10 mins after the administration of the first dose of the Moderna COVID vaccine, the patient fainted in the waiting room chair. I rendered first aid by calling out to him to rouse him. I provided him with water and apple slices as he complained of not having eaten for an extended period of time and being thirsty. He stated that he had no history of seizures, but had terrible anxiety. He also stated that he was still nervous about the vaccine even after administration. He sat in the pharmacy for almost an hour afterwards. In that time he finished off the apple slices and water bottle. He did not complain of any further symptoms and was able to leave the pharmacy under his own power.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Anxiety
- Vorgeschichte
- Anxiety
- Andere Medikamente
- None
- Allergien
- Nuts and sulfa drugs
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 25.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Asthenia
Contusion
Depressed mood
Electric shock sensation
Fatigue
Headache
Hot flush
Hypoaesthesia
Injection site pain
Injection site reaction
Injection site swelling
Intermenstrual bleeding
Loss of personal independence in daily activities
Muscle spasms
Muscle twitching
Pain
Pain in extremity
Symptomtext
Vaccine log moderna - 16th, Monday- twitching/spams in injection sight within the first hour of recovering vaccine. Otherwise feeling sore worse throughout day. Could barely undress for bed - 17th- very sore very painful if touched, or bumped still spasming around injection sight swelling - 18th- pretty sore but easing up. Very tiered. Spasm continue near injection sight - 19th- sore but subsiding a lot. Middle of night arm began going numb, tingling, needle/pin like sensation through arm to fingertips. Alternates between pinky,ring,middle going numb to pointer and thumb, to all. Muscle spams all over body. Anxious - 20TH very tired. Spasms continue, numbness is off and on but getting stronger. A little sore in injection sight still but not bad. Pin and needle sensation continuing through left arm still. Spasm occasionally in random areas of body. Tiered, mild headache. Called pharmacist she said it is a rare side effect go see doctor if left arm becomes painful or week. Went to emergency room, doctor said come back if I loose strength in arm but could just be ?my normal? response to vaccines. She said I am swollen and bruised , could be caused by swelling. She also said how the vaccines are new so they just don?t know yet why some people are responding the way they are. Prescribed Benadryl. I told the nurse I was nervous to get my second does and asked if she had advice. Nurse suggested asking to take another brand, I could have misinterpreted her. Also suggested taking Tylenol before second does. - 21st. Still slightly sore. Spams seem to calm down in the morning but would come back or get stronger throughout day. Feels more like ?vibrating? throughout arm or mild electricity going through it. Very tiered, feeling depressed and not heard or helped. Mild headache - 22nd Very depressed hot flashes and tired. My hand feels numb most of the time with electric shock feeling going through it or like a vibrating. Some spasms still. Getting random aches in right leg and Very mild pin feeling in leg. Mild headache, in areas of head I?ve never felt before. Tired. Started light spotting not supposed to start next menstrual cycle for 3 more days. - 23rd, hot flashes. Very mild Pain/mild numbness , arm spasming. Right leg has some numbness, pain. Mild headache, tired. Saw allergist said it seems like i am having anxiety induced symptoms. I can decide to take moderna again or a non mRNA vaccine. He says I am not having an allergic reaction and that my symptoms will stop once I decide. - 24th numb, hot flashes, sharp pains in arm woke me up twice while sleeping - 25th numb, left hand grip is getting weaker, saw chiropractor to see if adjustment would help. Gave some relief to sharp/needle pains temporarily. Arm is still numb. Arm becomes very tiered if I try to do anything to long
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- Asthma
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- I was 5 or 6 not sure which one . I had sever pain very deep throughout body. Felt like glass. Hallucinated.
- Staat
- NY
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 24.08.2021
- Beginn
- 24.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Fear of injection
Syncope
Vomiting
Symptomtext
-Patient has needle phobia -had syncope after vaccine and vomited.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 23.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Dizziness
Loss of consciousness
Symptomtext
Patient received Moderna first and was fine. I administered Adacel second and right after she tells me that she has a history of passing out from shots. She was sitting in a chair at the time of vaccination. She said she felt like she was going to pass out and slumped back in the chair and was out for about 30 seconds. She came to, and felt lightheaded for about 15 minutes, then she was ok. I stayed with her and gave her a bottle of water. Her husband was with us too.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- duloxetine 30 alprazolam 1
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 23.08.2021
- Impfdatum
- 23.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Nausea
Symptomtext
Patient reported feeling dizzy upon standing up after administered vaccine. Immediately passed out but was caught. Came right to within 20 seconds after passing out and reported feeling nausea for about 10 minutes after vaccine. Patient reports feeling ok after 30 minutes of observation and chose to leave facility prior to ambulance arriving due to long response time. Was advised to wait for medical evaluation by ambulance but chose to leave.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- pre-diabetes
- Vorgeschichte
- pre-diabetes possible per patient
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 17.08.2021
- Impfdatum
- 17.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Dizziness
Hypoaesthesia
Loss of consciousness
Vibratory sense increased
Symptomtext
2 minutes after the patient was injection, she explained that she felt lightheaded and dizzy and she passed out. once she regained consciousness she felt numb, could not feel her hands and feet and felt her entire body vibrating. i had her squeeze my hands and she was able to do so. we called 911 and upon ems arrival they monitored her blood pressure and blood sugar which were both within normal range. she was given water and orange juice and after 60 minutes felt good enough to go home with family member
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- blood pressure and blood glucose were both within normal ranges
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 07.08.2021
- Impfdatum
- 07.08.2021
- Beginn
- 07.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling hot
Syncope
Symptomtext
post vaccination, pt fainted at the front of the store. her husband caught her before she fell. she was provided with a seat to sit. offered her water but husband purchased some gatorade for her which she sipped on. was feeling better although felt a little hot. she decided to leave after waiting around the 15 minutes post vaccination to head home. pt reported after she fainted that this reaction had occurred before after giving blood but it was a long time ago.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- tried taking blood pressure with monitor and the digital monitor had errors on it. pt had smart watch and checked her pulse and it was 78 and was in normal sinus rhythm
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 30.11.2023
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Angiotensin II receptor type 1 antibody positive
Antinuclear antibody positive
Arthralgia
Asthenia
Biopsy lip normal
Blood test abnormal
COVID-19
Cardiac monitoring
Chest pain
Colonoscopy normal
Condition aggravated
Decreased appetite
Diarrhoea
Dizziness
Dyspnoea
Echocardiogram
Electrocardiogram
Electrocardiogram ambulatory abnormal
Symptomtext
Just like with the first dose I had long lasting arm pain and redness. I still had fatigue, changes in menstrual cycle, and appetite changes from the first dose of Moderna. Following this dose I had extreme Diarrhea, that was beyond what could be justified considering I didn't have an appetite and was losing weight prior due to not being able to eat much. Heart Palpitations started occasionally, I would describe them as very noticeable heart beats. I was able to catch what was happening on my smart watch ecg. My endurance for my usually walking or daily activities was less seemed out of breath or could have been from the fatigue from the initial vaccine. My migraines got substantially worse in frequency and intensity and no longer responded to treatment that had previously been successful. I caught covid in January shortly after the vaccine and recovered fine and then all of a sudden March 17, 2022 all symptoms worsened massively. I had chest pain, shortness of breath, tachycardia, POTS-like, MCAS-like, allergic type reactions to things I hadnt been allergic to before, diarrhea, no appetite, repulsed by foods, fatigue, light headedness, weak, shaky, body tremors, foreheah and leg numbness and tingling, worsening migraines that were non responsive to normal successful medications, joint pain, stiffness. The list goes on.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- SO much blood work I couldn't possibly list it all. Positive ANA and SSA/SSB: 8/31/2022 multiple visits some with positive and some negatives on the blood work Lip Biopsy for Sjogrens: 11/23/2023: No significant abnormalities Colonoscopy/Endoscopy: 9/23/2022: Unremarkable SIBO: Methane Dominate SIBO Positive: 11/1/2022 Transvaginal Ultrasound: 9/12/2022: Unremarkable Thyroid Ultrasound:9/18/2023: Unremarkable Multiple other tests: EKG, Echo of the Heart, MRI Heart, MRI Brain, Heart Monitors, Blood Pressure Monitors. Most tests come back structurally unremarkable. Blood tests most remain in limits with some out of limits such as: ANA, SSA, SSB, IRON-low iron storage has remained stable since iron infusion. I have tested positive for Angiotensin 2 type 1 receptor autoantibodies.
- Aktuelle Erkrankungen
- No other illnesses but I did have ongoing issues and changes in my body from the previous vaccine which was Moderna and was administered 9/3/2021. Following that vaccine I had arm pain and redness, fatigue outside of what is normal, changes in menstrual cycle, and complete loss of appetite.
- Vorgeschichte
- Migraines well controlled with Imitrex as needed.
- Andere Medikamente
- Imitrex as needed for Migraines
- Allergien
- Sulfa
- Vorherige Impfungen
- Moderna Vaccine Dose 1 on 09/01/2021 at age 34 just one month prior to this vaccine
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 17.08.2023
- Impfdatum
- 06.08.2021
- Beginn
- 13.01.2022
- Tage bis Beginn
- 160,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Complaining of shortness of breath and cough for the past few days. diagnosed covid positive one day ago with sx starting 5 days ago. Short course of remdesivir for 3 days. Decadron 6 mg daily. Azithromycin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 05.09.2022
- Impfdatum
- 14.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 18,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Magnetic resonance imaging
Muscle mass
Symptomtext
Loss of range of motion in left arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- Steorid shot Cortizone shots 2x Physical therapy Dry needling Massage MRI 8/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Loss of range of motion and muscle mass in left are after injections.
- Andere Medikamente
- Zoloft Claratin D
- Allergien
- Penicillen
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 24.09.2021
- Beginn
- 25.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Palpitations
Paraesthesia
Symptomtext
Numbness and tingling on the left side of my body from my left arm to my left foot on both injections. On the second injection palpitations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Tylenol 500 mg
- Allergien
- Latex
- Vorherige Impfungen
- Moderna.
- Staat
- PA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 25.08.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 68,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anticoagulant therapy
Arrhythmia
Atrial fibrillation
Blood test
Cardiac monitoring abnormal
Electrocardiogram abnormal
Ventricular tachycardia
Symptomtext
High grade arrhythmia including V tach. Saw Cardiology, and Electrophysiology. Elected observation. Subsequent developed afib requiring Eliquis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- Zio monitoring. EKG, Blood work.
- Aktuelle Erkrankungen
- S/P CVA, 12yrs S/P CABG 20 yrs
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Lisinopril, Toprol, Zetia, Cartia, Crestor
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 29.09.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 36,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Hypertension
Symptomtext
Before the vaccine my blood pressure was always below 130/80 often much lower. after the vaccine it went to around 160/100. it has stayed high. Went to Ramipril 5mg then and currently, 06/14/2022, 10mg and blood pressure is still around 150/90. I do not have a history of high blood pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetic
- Andere Medikamente
- metformin 1000mg, turmeric, Ramipril 1.25
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 15.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Paraesthesia
Symptomtext
Tingling in extremities (3 months), difficulty breathing (ongoing)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 08.08.2021
- Beginn
- 08.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Gait inability
Insomnia
Mobility decreased
Muscle tightness
Pain
Pain in extremity
Symptomtext
Arm hurts; Still has some tightness when he bends it in; Not being able to move his leg/could not straighten it/could not bend it; kept on waking up/ not sleeping last night; Throbbing; Left knee started hurting so bad/agonizing pain, agonizing joint pain in his left knee he describes it as a banging pain in the knee for multiple hours; He could not walk; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Arm hurts), GAIT INABILITY (He could not walk), MUSCLE TIGHTNESS (Still has some tightness when he bends it in), MOBILITY DECREASED (Not being able to move his leg/could not straighten it/could not bend it) and INSOMNIA (kept on waking up/ not sleeping last night) in a 40-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 08-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Aug-2021, the patient experienced GAIT INABILITY (He could not walk), MOBILITY DECREASED (Not being able to move his leg/could not straighten it/could not bend it), INSOMNIA (kept on waking up/ not sleeping last night), PAIN (Throbbing) and ARTHRALGIA (Left knee started hurting so bad/agonizing pain, agonizing joint pain in his left knee he describes it as a banging pain in the knee for multiple hours). On 09-Aug-2021, the patient experienced MUSCLE TIGHTNESS (Still has some tightness when he bends it in). On an unknown date, the patient experienced PAIN IN EXTREMITY (Arm hurts). On 09-Aug-2021, GAIT INABILITY (He could not walk), MOBILITY DECREASED (Not being able to move his leg/could not straighten it/could not bend it), INSOMNIA (kept on waking up/ not sleeping last night), PAIN (Throbbing) and ARTHRALGIA (Left knee started hurting so bad/agonizing pain, agonizing joint pain in his left knee he describes it as a banging pain in the knee for multiple hours) had resolved. At the time of the report, PAIN IN EXTREMITY (Arm hurts) and MUSCLE TIGHTNESS (Still has some tightness when he bends it in) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were reported. No treatment information was provided. Most recent FOLLOW-UP information incorporated above includes: On 09-Aug-2021: Reporter Information and event added. On 09-Aug-2021: Event details added
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 29.09.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Injection site pain
Product administered at inappropriate site
Ultrasound scan
X-ray
Symptomtext
Injection administered too high in left shoulder area, resulting in pain and loss of range of motion in shoulder.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- X-ray and ultrasound; MRI pending.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Tetracyclines; Sulfa drugs; Erythromycin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 09.08.2021
- Beginn
- 16.01.2022
- Tage bis Beginn
- 160,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dyspnoea
Fatigue
Pyrexia
SARS-CoV-2 test positive
Symptomtext
C/O cough,fevers,fatigue,SOB x 7 days. Diagnosed with COVID .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 3,0
- Labordaten
- Apparently had POSITIVE COVID test outside CentraState 6 days PTA
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes, Dyslipidemia, HTN, Obesity. Benign breast Bx. Smoking Status Never Smoker.
- Andere Medikamente
- aspirin (Aspirin Low Dose) 81 mg tablet,delayed release (DR/EC) Directions: 1 tablet oral daily (Active) atorvastatin (Lipitor) 40 mg Tablet Directions: 1 tablet oral daily at bedtime (Active) cloNIDine 0.2 mg/24 hour Patch Weekly Di
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 15.09.2021
- Beginn
- 09.01.2022
- Tage bis Beginn
- 116,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest X-ray abnormal
Dyspnoea
Dyspnoea exertional
Gout
Lung disorder
Pneumonia
SARS-CoV-2 test positive
Symptomtext
01/05/2022: Event occurred after 2nd vaccine. 52-year-old male past medical history Atrial fibrillation, hypertension, diabetes, hyperlipidemia, CAD, MI, CHF presenting for shortness of breath. Patient states that he has had progressively worsening dyspnea on exertion. Denies chest pain. Patient states that he has not had any near syncopal events or fevers or cough. GI: No abdominal pain, no nausea, no vomiting, no diarrhea. -Remdesivir (1/9 - ). receiving prednisone 40 mg daily for acute gout flare. remains in hospital on Jan 11 2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 6,0
- Labordaten
- 01/09/2022: COVID positive. 01/10/2022: chest xray- Interval worsening of airspace disease n both lungs. Correlate clinically with Pneumonia
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- history Atrial fibrillation, hypertension, diabetes, hyperlipidemia, CAD, MI, CHF
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 22.09.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 76,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Palpitations
Symptomtext
heart palpitations
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Heart attack survivor
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 21.08.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adnexa uteri pain
Condition aggravated
Hot flush
Hypoaesthesia
Postmenopausal haemorrhage
Smear cervix normal
Symptomtext
Left ovary pains. Numbness of right hand on palm and fingers. After 2nd shot, spotting and start of period after 6 years of menopause. Hot flashes started again after 4 years of ceasing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Pap smear- negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Lisinopril, Hydrochlorothiazide
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 08.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Chest pain
Glossodynia
Heart rate increased
Lymphoedema
Palpitations
Stomatitis
Stress echocardiogram
Supraventricular tachycardia
Symptomtext
Unexplained abdominal pain to the left of belly button after both injections that lasted 24 hours. Lymphedema in left arm post second shot that lasted 24 hours. Elevated heart rate and palpitations starting 10/09/2021 and resolved 10/24/2021. Chest pain that started 10/12/2021 and resolved 10/28/2021. Oral sores on tongue and gums started 10/21/2021 and still unresolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Stress Echo performed 10/22/2021 and came back normal but evidence of SVT.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- Allergy to carrots, apples, nuts, kiwi, shellfish
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 26.09.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate
Insomnia
Loss of personal independence in daily activities
Nausea
Nightmare
Palpitations
Tremor
Symptomtext
Couldn't drive, so she called off work; Felt nauseated; Heart was pounding so hard in my chest; she could hear it in her left ear; Body jolted; Terrible nightmare/ nightmare all over again, this happened all night long; Woke up at least 20 times or more / insomnia; This spontaneous case was reported by a consumer and describes the occurrence of PALPITATIONS (Heart was pounding so hard in my chest; she could hear it in her left ear), TREMOR (Body jolted), NIGHTMARE (Terrible nightmare/ nightmare all over again, this happened all night long), INSOMNIA (Woke up at least 20 times or more / insomnia) and LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (Couldn't drive, so she called off work) in a 47-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 026D21 and 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was provided by the reporter. Concomitant products included FEXOFENADINE HYDROCHLORIDE (ALLEGRA) for an unknown indication. On 26-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 24-Oct-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 24-Oct-2021, the patient experienced PALPITATIONS (Heart was pounding so hard in my chest; she could hear it in her left ear), TREMOR (Body jolted), NIGHTMARE (Terrible nightmare/ nightmare all over again, this happened all night long), INSOMNIA (Woke up at least 20 times or more / insomnia) and NAUSEA (Felt nauseated). On 25-Oct-2021, the patient experienced LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (Couldn't drive, so she called off work). At the time of the report, PALPITATIONS (Heart was pounding so hard in my chest; she could hear it in her left ear), TREMOR (Body jolted), NIGHTMARE (Terrible nightmare/ nightmare all over again, this happened all night long), INSOMNIA (Woke up at least 20 times or more / insomnia), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (Couldn't drive, so she called off work) and NAUSEA (Felt nauseated) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 24-Oct-2021, Heart rate: 130 (High) Increased. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211024; Test Name: Heart rate; Result Unstructured Data: Increased
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- ALLEGRA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 21.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Nausea
Pain
Palpitations
Symptomtext
18 hours in - nausea. Lasted 3 days after. 24 hours in - woke up in middle of night with racing heart. 3 days in - arm pain at site. Still going on 6 days in - full body aches. Still going on.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma (2 months)
- Andere Medikamente
- Inhaler, allergy medicibe
- Allergien
- None aware of
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 29.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
Headache
Heart rate
Heart rate decreased
Hypertension
Myalgia
Palpitations
Symptomtext
Serious palpitations; Lower number of blood pressure was high; Lower heart rate; Muscle ache; Headache; This spontaneous case was reported by a nurse and describes the occurrence of PALPITATIONS (Serious palpitations), HYPERTENSION (Lower number of blood pressure was high), HEART RATE DECREASED (Lower heart rate), MYALGIA (Muscle ache) and HEADACHE (Headache) in a 33-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Sep-2021, the patient experienced PALPITATIONS (Serious palpitations), HYPERTENSION (Lower number of blood pressure was high), HEART RATE DECREASED (Lower heart rate), MYALGIA (Muscle ache) and HEADACHE (Headache). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency and IBUPROFEN for Adverse event, at an unspecified dose and frequency. At the time of the report, PALPITATIONS (Serious palpitations), HYPERTENSION (Lower number of blood pressure was high), HEART RATE DECREASED (Lower heart rate), MYALGIA (Muscle ache) and HEADACHE (Headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 30-Sep-2021, Blood pressure measurement: high (High) lower number of blood pressure was high.. On 30-Sep-2021, Heart rate: 56 (Low) lower heart rate (56 bpm) for 2 weeks.. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. It was reported that the patient had serious palpitations, lower number of blood pressure was high, headache, muscle ache, and lower heart rate (56 bpm) for 2 weeks. The headache and muscle ache were coming and going. And all the symptoms started together the next day after first shot. No Concomitant medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210930; Test Name: BLOOD PRESSURE; Result Unstructured Data: lower number of blood pressure was high.; Test Date: 20210930; Test Name: HEART RATE; Result Unstructured Data: lower heart rate (56 bpm) for 2 weeks.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 22.10.2021
- Impfdatum
- 29.09.2021
- Beginn
- 07.10.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenopia
Erythema
Facial discomfort
Feeling hot
Hypoaesthesia
Injection site rash
Limb discomfort
Pain
Pain in extremity
Paraesthesia
Pruritus
Rash papular
Swelling
Tenderness
Symptomtext
Large rash area of injection site 5 inches in diameter. Red, raised bumpy. Painful, itchy and hot to touch. In 24 hours doubled in size. Pain down arm. Redness, swelling went away 1 week later. A day later numbness, tingling pain left side of face up into head and ear. Extremely painful to touch. Left side of throat, teeth upper and lower. 3 days later left leg be an bothering. Felt better 5 days later. Left side of face still uncomfortable, left eyelid feels heavy still.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Levothyroxine
- Allergien
- Apples
- Vorherige Impfungen
- 34 flu shot
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 02.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Arthralgia
Asthenia
Condition aggravated
Diarrhoea
Dizziness
Dyspnoea
Eye pain
Headache
Hypokinesia
Lacrimation increased
Myalgia
Nausea
Peripheral coldness
Photophobia
SARS-CoV-2 test
Throat irritation
Throat tightness
Symptomtext
Eyes are teary; Can't tolerate light; Pain in her eyes; Her throat is irritated; Can't move much; Started to feel her feet very cold; Very very weak; Feels her throat closes; Her breathing gets a little heavy; Pain in all her body / When she goes to sleep is like laying on a bed of nails; Very dizzy/a lot of dizziness; Stomach ache that expanded, it was very strange/very bad stomach ache on 05 Oct/pain in her stomach; Diarrhea; Arthritis in one shoulder and this made it worse; Bad nausea/a lot of nausea; A lot of joint pain/pain in her joints on 04 Oct 2021; headache/pain in her head; This spontaneous case was reported by a consumer and describes the occurrence of THROAT IRRITATION (Her throat is irritated), HYPOKINESIA (Can't move much), PERIPHERAL COLDNESS (Started to feel her feet very cold), ASTHENIA (Very very weak) and THROAT TIGHTNESS (Feels her throat closes) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 on 06-Aug-2021. Concurrent medical conditions included Arthritis. On 01-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Oct-2021, the patient experienced ARTHRALGIA (A lot of joint pain/pain in her joints on 04 Oct 2021) and HEADACHE (headache/pain in her head). On 04-Oct-2021, the patient experienced PERIPHERAL COLDNESS (Started to feel her feet very cold), ASTHENIA (Very very weak), THROAT TIGHTNESS (Feels her throat closes), DYSPNOEA (Her breathing gets a little heavy), DIZZINESS (Very dizzy/a lot of dizziness), ABDOMINAL PAIN UPPER (Stomach ache that expanded, it was very strange/very bad stomach ache on 05 Oct/pain in her stomach), DIARRHOEA (Diarrhea), CONDITION AGGRAVATED (Arthritis in one shoulder and this made it worse), NAUSEA (Bad nausea/a lot of nausea) and MYALGIA (Pain in all her body / When she goes to sleep is like laying on a bed of nails). On 05-Oct-2021, the patient experienced THROAT IRRITATION (Her throat is irritated) and HYPOKINESIA (Can't move much). On an unknown date, the patient experienced LACRIMATION INCREASED (Eyes are teary), PHOTOPHOBIA (Can't tolerate light) and EYE PAIN (Pain in her eyes). At the time of the report, THROAT IRRITATION (Her throat is irritated), HYPOKINESIA (Can't move much), PERIPHERAL COLDNESS (Started to feel her feet very cold), ASTHENIA (Very very weak), THROAT TIGHTNESS (Feels her throat closes), DYSPNOEA (Her breathing gets a little heavy), LACRIMATION INCREASED (Eyes are teary), PHOTOPHOBIA (Can't tolerate light), EYE PAIN (Pain in her eyes), DIZZINESS (Very dizzy/a lot of dizziness), ABDOMINAL PAIN UPPER (Stomach ache that expanded, it was very strange/very bad stomach ache on 05 Oct/pain in her stomach), DIARRHOEA (Diarrhea), CONDITION AGGRAVATED (Arthritis in one shoulder and this made it worse), NAUSEA (Bad nausea/a lot of nausea), ARTHRALGIA (A lot of joint pain/pain in her joints on 04 Oct 2021), HEADACHE (headache/pain in her head) and MYALGIA (Pain in all her body / When she goes to sleep is like laying on a bed of nails) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: negative (Negative) Negative. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No relevant concomitant medications were reported. No treatment information was reported. Company comment: This case concerns a 51-year-old female patient with no relevant medical history, who experienced the expected event of Arthralgia. The event occurred one day after receiving the first dose of mRNA-1273 (Moderna COVID-19 Vaccine). The rechallenge was not applicable since only information about the first dose was disclosed. The event is consistent with the current understanding of the mechanism of action of the vaccine. The benefit-risk relationship of mRNA-1273 (Moderna COVID-19 Vaccine) is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 07-Oct-2021: Follow-up received on 08 Oct 2021 contains no new information.; Sender's Comments: This case concerns a 51-year-old female patient with no relevant medical history, who experienced the expected event of Arthralgia. The event occurred one day after receiving the first dose of mRNA-1273 (Moderna COVID-19 Vaccine). The rechallenge was not applicable since only information about the first dose was disclosed. The event is consistent with the current understanding of the mechanism of action of the vaccine. The benefit-risk relationship of mRNA-1273 (Moderna COVID-19 Vaccine) is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Test Name: SARS-CoV-2 test; Test Result: Negative ; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- Arthritis
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 15.10.2021
- Impfdatum
- 16.08.2021
- Beginn
- 26.08.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthma
Cough
Dyspnoea
Extra dose administered
Lymphadenopathy
Nasal inflammation
Symptomtext
My lungs were not happy when I started 8/16/2021. So I did use the nebulizer that day. That may not necessarily relate to the vaccine because I already had problems. But then I felt better and didn't use my nebulizer for several days. But by the time it was the 8/26, that's when my lungs did not start feeling good again. So I had to use my nebulizer again. On the 8/27, I was having my asthma cough again. And I couldn't talk without struggling to breathe. And I had to use my c-pap again but then I couldn't get that to seal properly because nasal tissue was inflamed. On 8/28 that's when I realized that my neck lymph nodes were really swollen. And I did not have that reaction to the prior 2 vaccinations. By 8/29 I could see that the swelling on my neck lymph nodes were going down. And the 9/1 I noted that I was having trouble speaking sentences without the asthma cough again. And I was using the nebulizer and trying to self manage with the nebulizer. I was using the nebulizer every day and then starting 9/22 that's when the doctor told me to use my maintenance inhaler twice a day for two weeks. So when I did the inhaler I did 2 puffs total of 4 puffs daily for two weeks. The last day of twice a day inhaler was 10/5 and I stopped the daily nebulizer on 10/2/2021. 10/6 return to maintenance inhaler once a day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Wildfire smoke was irritating lungs over Summer 2021, dehydration - certain times of the day
- Vorgeschichte
- Fibromyalgia; Osteoarthritis; Osteopenia; Idiopathic Thrombocytopenia Purpura; Interstitial Cystitis; IBS; Asthma or Reactive Airway Disease; Sleep Apnea; Subclinical Hypothyroid; Adrenal and Pituitary Insufficiency; Vocal Chord Dysfunction; Pelvic Floor Dysfunction; Psoriasis; Lipodermatosclerosis
- Andere Medikamente
- Levothyroxine - 50 mcg 6 days a week; Misoprostol - 200 mcg twice daily; Cyclobenzaprine - 5mg once daily; Alprazolam - 0.5mg daily; Elmiron - 100mg 3x daily; Detrol 2mg once daily; Etodolac ? 600mg once daily; Atrovent nasal spray 42 mcg 2
- Allergien
- Bactrim; Rhinocort; Tofranil; Tedral; Ibuprofen; Sudafed; Elavil; Ditropan; Salsalate; Clinoril; Prilosec; Minipress; Celebrex; Prevacid; Hydroxyzine; Dextra; Tegaderm; Serevent; Mold allergy; Volatile Organic Compound (can't walk in aisles with soap - undiagnosed)
- Vorherige Impfungen
- 03/12/2021 (Age 57) - 1st COVID Moderna vaccine - head felt very spacey and wrong, Probably affected blood pressure
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 08.10.2021
- Impfdatum
- 15.09.2021
- Beginn
- 16.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Computerised tomogram
Heart rate increased
Hypertension
Injection site urticaria
Migraine
Myalgia
Nausea
Pain in extremity
Speech disorder
Tremor
Vomiting
Symptomtext
Hives around injection site after 24 hours. Body shaking after 3 days. We have been to the ER 6 times in 4 weeks for uncontrolled body shakes, High blood pressure, Nausea and vomiting. Muscle soreness in arm and difficulty talking. Painful migraine like headache Heart rate elevated. This is a nightmare for my wife as the ER doctors just throw painkillers at her. The second dose has changed my wife. Please. Please help
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Ct scan blood work. No MRI. No X-ray to check fir Myocardial issue
- Aktuelle Erkrankungen
- Allergies
- Vorgeschichte
- None
- Andere Medikamente
- Tylenol. Birth control.
- Allergien
- Apples
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 03.10.2021
- Impfdatum
- 23.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Blepharospasm
Blood test normal
Chest X-ray normal
Dizziness
Dyspnoea
Ear pain
Electrocardiogram normal
Fatigue
Hyperhidrosis
Insomnia
Myalgia
Neck pain
Palpitations
Symptomtext
fatigue, shortness of breath, heart palpitations, eye twitching, sweating, dizzy spells - all for 9 days. Neck muscle pain radiating to the ear-for two days. Anxiety and unable to sleep- still present
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Chest xray, EKG, blood work showed no clinical issues. all was done at urgent care on September 30th.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- vit D, Vit C, Zinc
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 16.08.2021
- Beginn
- 19.09.2021
- Tage bis Beginn
- 34,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Chest X-ray normal
Chest pain
Computerised tomogram normal
Discomfort
Ear discomfort
Head discomfort
Headache
Inflammation
Magnetic resonance imaging normal
Middle ear inflammation
Myalgia
Neck pain
Pain
Pain in extremity
SARS-CoV-2 test negative
Temporomandibular joint syndrome
Symptomtext
I started feeling a pressure from my shoulders up into my head. My ears had so much pressure like I was on a plane but they wouldn't pop. I had zero congestion though. Went to Dr the 8/20/2021 and had a fever of 99.7 & was told I was having inflammation from the vaccination & to take some muscle relaxers for 7-10 days. The pressure in my head and ears was so bad I went to Dr a week later & she said she has also been seeing this and I am having inflammtion from the vaccination. No fluid in my ears & externely everything looked fine. She said my eustachian tubes were inflammed. She suggested nasacort, sudafed, & 600 mg of ibuprphen daily for the next week.Also had a slight case of TMJ from the imflammation so told to try soft foods for the week as well. Went back to Dr. & she decied we try Predniose for 10 days. 40 mg for 5 days and 20 mg for 5 days. I made it without any releif to day 6 and ended up going to the ER for chest pains & the headache. They took a CT Scan, chest xray, blood work, & covid test. Everything came back looking good so said they also believed I was having an adverse reaction to the vaccination. They then put me on Lorazpam for 5 days to try to sleep because the back of my head is so paingul and they pressure in my head gets worse as the time goes on. They also suggested ibuprophen & acetaminophen as well. MRI was done a few days later & everything came back looking good with that too. I am still having pressure in my head, shooting pains in neck, muscle pain in my shoulders & some pain in my right arm. I am trying to get into more doctors but everyone is backed up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 9/14/2021 CT Scan, bloodwork, chest xray, covid test all good. 9/23/2021 MRI came back good as well
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- mganesium, fish oil, D3, and Calcium
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 29.09.2021
- Impfdatum
- 10.08.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 23,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Headache
Inappropriate schedule of product administration
Migraine
Neck pain
Pain in extremity
Vaccination site pain
Symptomtext
The sharp pains start on the left side of my head, go down my left neck & arm, then I feel it in my stomach. I have it every few days.; The sharp pains start on the left side of my head, go down my left neck & arm, then I feel it in my stomach. I have it every few days.; The sharp pains start on the left side of my head, go down my left neck & arm, then I feel it in my stomach. I have it every few days.; I get migraines every day now.; I still get sharp pains in my head, periodically.; 1st dose on 10th Aug and 2nd dose on 2Sep; I had migraines that lasted for days at a time that would each last a few hrs at a time, then goes away.; It was so painful at the injection site; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (The sharp pains start on the left side of my head, go down my left neck & arm, then I feel it in my stomach. I have it every few days.), NECK PAIN (The sharp pains start on the left side of my head, go down my left neck & arm, then I feel it in my stomach. I have it every few days.), ABDOMINAL PAIN UPPER (The sharp pains start on the left side of my head, go down my left neck & arm, then I feel it in my stomach. I have it every few days.), MIGRAINE (I get migraines every day now.) and MIGRAINE (I had migraines that lasted for days at a time that would each last a few hrs at a time, then goes away.) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 040C21A and 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Bell's palsy in 2008. Concurrent medical conditions included Migraine. On 10-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 02-Sep-2021, the patient experienced MIGRAINE (I had migraines that lasted for days at a time that would each last a few hrs at a time, then goes away.), VACCINATION SITE PAIN (It was so painful at the injection site) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st dose on 10th Aug and 2nd dose on 2Sep). On 20-Sep-2021, the patient experienced PAIN IN EXTREMITY (The sharp pains start on the left side of my head, go down my left neck & arm, then I feel it in my stomach. I have it every few days.), NECK PAIN (The sharp pains start on the left side of my head, go down my left neck & arm, then I feel it in my stomach. I have it every few days.), ABDOMINAL PAIN UPPER (The sharp pains start on the left side of my head, go down my left neck & arm, then I feel it in my stomach. I have it every few days.), MIGRAINE (I get migraines every day now.) and HEADACHE (I still get sharp pains in my head, periodically.). The patient was treated with PARACETAMOL (TYLENOL) for Migraine, at a dose of 650 mg. On 02-Sep-2021, VACCINATION SITE PAIN (It was so painful at the injection site) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st dose on 10th Aug and 2nd dose on 2Sep) had resolved. At the time of the report, PAIN IN EXTREMITY (The sharp pains start on the left side of my head, go down my left neck & arm, then I feel it in my stomach. I have it every few days.), NECK PAIN (The sharp pains start on the left side of my head, go down my left neck & arm, then I feel it in my stomach. I have it every few days.), ABDOMINAL PAIN UPPER (The sharp pains start on the left side of my head, go down my left neck & arm, then I feel it in my stomach. I have it every few days.), MIGRAINE (I get migraines every day now.) and HEADACHE (I still get sharp pains in my head, periodically.) had not resolved and MIGRAINE (I had migraines that lasted for days at a time that would each last a few hrs at a time, then goes away.) had resolved. No concomitant medication was reported. Patient stated that she has titanium in both her wrists and her jaw. She also stated that her doctor has advised her to get a CAT scan of her brain because of migraines as the doctor said that could be due to bleeding in her brain but the patient has not yet got the scan and said that she has had bad experiences. Always gritting teeth from pain. This case was linked to MOD-2021-325490 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Migraine
- Vorgeschichte
- Medical History/Concurrent Conditions: Bell's palsy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 28.09.2021
- Impfdatum
- 10.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Feeling abnormal
Migraine
Nausea
Symptomtext
I started having intense migraines; I felt off balance, like when I 1st get out of bed, I would fall against the wall.; I felt nauseous; I felt horrible for the 1st 5 days./ felt so heavy, like liquid cement/felt like water in my head; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (I felt horrible for the 1st 5 days./ felt so heavy, like liquid cement/felt like water in my head), MIGRAINE (I started having intense migraines), BALANCE DISORDER (I felt off balance, like when I 1st get out of bed, I would fall against the wall.) and NAUSEA (I felt nauseous) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Concomitant products included PARACETAMOL (TYLENOL) for an unknown indication. On 10-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Aug-2021, the patient experienced FEELING ABNORMAL (I felt horrible for the 1st 5 days./ felt so heavy, like liquid cement/felt like water in my head). On 11-Aug-2021, the patient experienced MIGRAINE (I started having intense migraines), BALANCE DISORDER (I felt off balance, like when I 1st get out of bed, I would fall against the wall.) and NAUSEA (I felt nauseous). At the time of the report, FEELING ABNORMAL (I felt horrible for the 1st 5 days./ felt so heavy, like liquid cement/felt like water in my head), MIGRAINE (I started having intense migraines), BALANCE DISORDER (I felt off balance, like when I 1st get out of bed, I would fall against the wall.) and NAUSEA (I felt nauseous) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. No treatment medication provided This case was linked to MOD-2021-326700 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- TYLENOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 23.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Dyspepsia
Hyperacusis
Paraesthesia
Symptomtext
Arm burning then spread to hands and feet and also stomach . Amplified sounds . Arm pit felt like pins and needles
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- high blood pressure irregular heart beat thyroid
- Andere Medikamente
- Losartan Potassium levothyroxine rosuvastatin chlorthalidone
- Allergien
- z-pac demurral
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 24.09.2021
- Impfdatum
- 13.08.2021
- Beginn
- 14.09.2021
- Tage bis Beginn
- 32,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dehydration
Dyspnoea
Symptomtext
Trouble breathing; Dehydrated; This spontaneous case was reported by a pharmacist and describes the occurrence of DYSPNOEA (Trouble breathing) and DEHYDRATION (Dehydrated) in a 35-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 046C21A and 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 14-Sep-2021, the patient experienced DYSPNOEA (Trouble breathing) (seriousness criterion hospitalization) and DEHYDRATION (Dehydrated) (seriousness criterion hospitalization). At the time of the report, DYSPNOEA (Trouble breathing) and DEHYDRATION (Dehydrated) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product was not provided by the reporter. Patient reported that On 14-sep-2021, the patient went for walk and experienced trouble breathing. Treatment information was not provided. Company Comment: This case concerns a 35-year-old, male patient with no previous relevant medical history, who experienced the unexpected events of dyspnoea and dehydration. The events occurred 1 day after the second dose of mRNA-1273. The rechallenge was not applicable since only information about the first dose was disclosed. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This case concerns a 35-year-old, male patient with no previous relevant medical history, who experienced the unexpected events of dyspnoea and dehydration. The events occurred 1 day after the second dose of mRNA-1273. The rechallenge was not applicable since only information about the first dose was disclosed. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 23.09.2021
- Impfdatum
- 17.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Dyspnoea
Fatigue
Feeling abnormal
Peripheral swelling
Symptomtext
shortness of breath sometimes; Swelling in the legs; Blisters, blisters are like a sunburn, water blisters, blisters are starting to open up and sip; No energy; Ever since she got the first dose she has felt very very crummy,everything started and it got progressively worse, Sometimes she feels better, sometimes worse; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (Ever since she got the first dose she has felt very very crummy,everything started and it got progressively worse, Sometimes she feels better, sometimes worse), DYSPNOEA (shortness of breath sometimes), PERIPHERAL SWELLING (Swelling in the legs), BLISTER (Blisters, blisters are like a sunburn, water blisters, blisters are starting to open up and sip) and FATIGUE (No energy) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Concurrent medical conditions included Arthritis (In knees). On 17-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Aug-2021, the patient experienced FEELING ABNORMAL (Ever since she got the first dose she has felt very very crummy,everything started and it got progressively worse, Sometimes she feels better, sometimes worse). On an unknown date, the patient experienced DYSPNOEA (shortness of breath sometimes), PERIPHERAL SWELLING (Swelling in the legs), BLISTER (Blisters, blisters are like a sunburn, water blisters, blisters are starting to open up and sip) and FATIGUE (No energy). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency and NAPROXEN SODIUM (ALEVE) for Adverse event, at an unspecified dose and frequency. At the time of the report, FEELING ABNORMAL (Ever since she got the first dose she has felt very very crummy,everything started and it got progressively worse, Sometimes she feels better, sometimes worse), DYSPNOEA (shortness of breath sometimes), PERIPHERAL SWELLING (Swelling in the legs), BLISTER (Blisters, blisters are like a sunburn, water blisters, blisters are starting to open up and sip) and FATIGUE (No energy) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient regularly checked blood pressure, and states for the past month it has not been right. Patient mentions that the most difference are in the bottom numbers, which are higher than normal. No relevant concomitant medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Arthritis (In knees)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 22.09.2021
- Impfdatum
- 25.08.2021
- Beginn
- 25.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Migraine
Symptomtext
migraines and chest tightness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- none known
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 18.09.2021
- Impfdatum
- 18.08.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Dyspnoea
Symptomtext
Patient came in for 2nd moderna covid 19 vaccine appointment. I was asking him if he had experienced any issues with the first shot. He stated he had intermittent chest pain starting a few days after the vaccine that was accompanied with mild shortness of breath which was not normal for him. The intermittent chest pain and SOB lasted about a week and has since resolved. Patient stated he had a physical after the vaccine. He mentioned the symptoms and his vaccination status to the doctor. He said the doctor listened to his heart and said he thought it was allergies. Patient stated he does not have allergies and didn't think it was allergies. We decided to hold off on the 2nd vaccine until we could talk to the doctor (patient came in for 2nd vaccine on a saturday when md office was closed).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- unknown- pt has physical after vaccine on an unknown date
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- no known
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 17.09.2021
- Impfdatum
- 13.08.2021
- Beginn
- 05.09.2021
- Tage bis Beginn
- 23,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood thyroid stimulating hormone decreased
Cardiac stress test
Chest discomfort
Condition aggravated
Dizziness
Echocardiogram
Electrocardiogram abnormal
Eructation
Heart rate irregular
Laboratory test
Nausea
Symptomtext
NAUSEA LIGHTHEADED . CHEST PRESSURE. CONSTANT BELCHING. SAW PRIMARY PHYSICIAN ON 9/13/21 . EKG SHOWED ABNORMAL HEARBEAT . WA REFERED TO CARDIOLOGIST . SAW CARDIOLOGIST ON 9/14/21 REQUESTED LAB AND TEST
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- ECHO MONITOR AND STRESS TEST . RESULTS NOT IN . ALSO LABWORK TSH CAM BACK GELOW NORMAL RANGE. TSH HASN'T BEEN LOW IN 20
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HYPOTHYROIDISM
- Andere Medikamente
- LEVOTHYROXINE 0.15 MG BENAZAPRIL 20MG VITAMIN A C D E AND ZINC . MAGNESIUM 250MG ELDERBERRY 3800 MG . PEPCID AC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 23.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
Fatigue
Grip strength decreased
Headache
Tinnitus
Tremor
Symptomtext
She drops things; Kind of a headache; Felt tired for the first couple of days; Got tinnitus, can only hear whistles and noise; Shaking, hands are shaking / hand shaking; This spontaneous case was reported by a consumer and describes the occurrence of TINNITUS (Got tinnitus, can only hear whistles and noise), TREMOR (Shaking, hands are shaking / hand shaking), GRIP STRENGTH DECREASED (She drops things), HEADACHE (Kind of a headache) and FATIGUE (Felt tired for the first couple of days) in an 82-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Concurrent medical conditions included Allergy to antibiotic. On 23-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Aug-2021, the patient experienced TREMOR (Shaking, hands are shaking / hand shaking). On 27-Aug-2021, the patient experienced TINNITUS (Got tinnitus, can only hear whistles and noise). On an unknown date, the patient experienced GRIP STRENGTH DECREASED (She drops things), HEADACHE (Kind of a headache) and FATIGUE (Felt tired for the first couple of days). At the time of the report, TINNITUS (Got tinnitus, can only hear whistles and noise), TREMOR (Shaking, hands are shaking / hand shaking), GRIP STRENGTH DECREASED (She drops things), HEADACHE (Kind of a headache) and FATIGUE (Felt tired for the first couple of days) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 23-Aug-2021, Blood pressure measurement: increased (High) Blood pressure increased. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. The patient did not take any medication for the adverse events and does not take any concomitant medications. Most recent FOLLOW-UP information incorporated above includes: On 05-Sep-2021: Patient medical history and lab data were added. Event verbatim was changed and hand shaking event date was added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210823; Test Name: Blood pressure; Result Unstructured Data: Blood pressure increased
- Aktuelle Erkrankungen
- Allergy to antibiotic
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 10.09.2021
- Impfdatum
- 27.08.2021
- Beginn
- 27.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Symptomtext
patient states that she has been having trouble using her arm since receiving her booster covid vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 05.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Symptomtext
Patient felt chest pain the following day (Saturday 9/4) after the second dose and called the pharmacy on Sunday to inform us of his symptom.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- no test performed.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 19.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Rash
Urticaria
Symptomtext
A difficult time breathing; Welts all over his body; A full blown rash / rash kind of resolving; This spontaneous case was reported by a pharmacist and describes the occurrence of DYSPNOEA (A difficult time breathing), URTICARIA (Welts all over his body) and RASH (A full blown rash / rash kind of resolving) in a 24-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Aug-2021, the patient experienced DYSPNOEA (A difficult time breathing), URTICARIA (Welts all over his body) and RASH (A full blown rash / rash kind of resolving). At the time of the report, DYSPNOEA (A difficult time breathing) and URTICARIA (Welts all over his body) had resolved and RASH (A full blown rash / rash kind of resolving) was resolving. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The pharmacist recommended Benadryl to the patient. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. However, very limited information regarding these events has been provided at this time. Case downgraded to non-serious due to the lack of evidence of seriousness from a regulatory or clinical standpoint, given that medical intervention was not needed. Further information is not expected.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. However, very limited information regarding these events has been provided at this time. Case downgraded to non-serious due to the lack of evidence of seriousness from a regulatory or clinical standpoint, given that medical intervention was not needed. Further information is not expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.09.2021
- Impfdatum
- 08.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Eye pain
Headache
Nausea
Neuralgia
Pyrexia
Symptomtext
Pt. states that after receiving the 1st dose of Moderna 08/08/2021, started experiencing symptoms 08/09/2021 of shortness of breath, dull headaches with nerve pain in the back of the neck, pain between eyes, and fever (101.0). Primary appt. 09/14/2021. 08/13/2021 shortness of breath episode happened again (hospice provided air tank), nausea, and mild headache continue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Stage 4 Lung Cancer Pt.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 31.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Headache
Infection
Injected limb mobility decreased
Malaise
SARS-CoV-2 test negative
Upper-airway cough syndrome
Vaccination site swelling
Symptomtext
It swelled all around the vaccine site. The size of a soft ball. I could hardly move my arm at all. The doctor drew a circle around where it appeared to be infected to make sure it did not go outside that area. They were not able to do anything about it. They asked me to take Benadryl, iced it, and continue to watch it. They did a COVID test and it was negative. After that I continued to keep a headache and I was really sick. I felt like I had COVID for about 4 days. The injection site is much better. Since then I have been keeping a really bad headache, nasal drip, and cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- COVID test- negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 19.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Rash
Urticaria
Symptomtext
Patient developed welt type rash all over body and felt he had hard time breathing. Reaction started hours after vaccine. Came to pharmacy 6 days later. I spoke with his caregiver. Patient reported breathing ok now + rash slowly resolving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Not known
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 08.08.2021
- Beginn
- 08.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Axillary pain
Diarrhoea
Dizziness
Erythema
Fatigue
Feeling abnormal
Feeling hot
Headache
Limb discomfort
Mobility decreased
Myalgia
Nausea
Restlessness
Vaccination site erythema
Vaccination site pruritus
Vaccination site warmth
Vomiting
Symptomtext
still gets a little queasy; site of injection got really red; body aches/muscle aches; feels fatigued; saw soreness under her armpit; couldn't barely get out of bed; arm was really bothering; lump under her armpit; (lump) red; (lump) hot; location of vaccination is hot to the touch,site of injection got really hot; Diarrhea; dizziness; felt really bad; restlessness; location of vaccination is very itchy,(lump) itchy; Vomit; had a splitting headache/terrible headaches/Still has a headache but it is not lingering; This spontaneous case was reported by a consumer and describes the occurrence of MOBILITY DECREASED (couldn't barely get out of bed), LIMB DISCOMFORT (arm was really bothering), AXILLARY MASS (lump under her armpit), ERYTHEMA ((lump) red) and FEELING HOT ((lump) hot) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 in February 2021. Family history included Allergy to vaccine since an unknown date. Concomitant products included GABAPENTIN, LEVOTHYROXINE and METHOCARBAMOL for an unknown indication. On 08-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Aug-2021, the patient experienced HEADACHE (had a splitting headache/terrible headaches/Still has a headache but it is not lingering). On 09-Aug-2021, the patient experienced MOBILITY DECREASED (couldn't barely get out of bed), LIMB DISCOMFORT (arm was really bothering), AXILLARY MASS (lump under her armpit), ERYTHEMA ((lump) red), FEELING HOT ((lump) hot), VACCINATION SITE WARMTH (location of vaccination is hot to the touch,site of injection got really hot), DIARRHOEA (Diarrhea), DIZZINESS (dizziness), FEELING ABNORMAL (felt really bad), RESTLESSNESS (restlessness), VACCINATION SITE PRURITUS (location of vaccination is very itchy,(lump) itchy), VOMITING (Vomit), VACCINATION SITE ERYTHEMA (site of injection got really red), MYALGIA (body aches/muscle aches), FATIGUE (feels fatigued) and AXILLARY PAIN (saw soreness under her armpit). On an unknown date, the patient experienced NAUSEA (still gets a little queasy). At the time of the report, MOBILITY DECREASED (couldn't barely get out of bed), LIMB DISCOMFORT (arm was really bothering), AXILLARY MASS (lump under her armpit), ERYTHEMA ((lump) red), FEELING HOT ((lump) hot), VACCINATION SITE WARMTH (location of vaccination is hot to the touch,site of injection got really hot), DIARRHOEA (Diarrhea), DIZZINESS (dizziness), FEELING ABNORMAL (felt really bad), RESTLESSNESS (restlessness), VACCINATION SITE PRURITUS (location of vaccination is very itchy,(lump) itchy), VOMITING (Vomit), NAUSEA (still gets a little queasy), VACCINATION SITE ERYTHEMA (site of injection got really red), MYALGIA (body aches/muscle aches), FATIGUE (feels fatigued), AXILLARY PAIN (saw soreness under her armpit) and HEADACHE (had a splitting headache/terrible headaches/Still has a headache but it is not lingering) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment information was not provided. It was reported that the patient had COVID in February and was very sick but ended up recovering from it. She received supplements. She received the vaccine in her upper arm muscle. She stated that today is the first day she was able to sit up and stay out of bed. She wanted to know if her symptoms were normal if she had to wait it out or not if she could put ice in her arm. She also stated that her son had an allergy to MMR vaccine when he was 18 months old and was wondering if he can receive the Moderna COVID19 Vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to vaccine
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- GABAPENTIN; LEVOTHYROXINE; METHOCARBAMOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 26.08.2021
- Impfdatum
- 23.08.2021
- Beginn
- 24.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Dyspnoea
Laboratory test
Palpitations
Tremor
Symptomtext
Difficulty breathing, heart racing, legs and hands were shaking, and he felt chills.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Various Tests Ran
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 25.08.2021
- Impfdatum
- 12.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Paraesthesia
Peripheral swelling
Swelling face
Symptomtext
The patient reported feeling numbness and tingling that radiated from her right arm to the right side (cheek area) of her face. She also experienced swelling from the arm to the face. She stated that the symptoms resolved about a day later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pruritus
Nausea
Palpitations
Pruritus
Symptomtext
Around 6 :45 injection area very itchy. By 7 extreme itchiness, By 7:45 shoulder to elbow extreme itch debated if I should contact pharmacy. Around 8 p.m. I noticed heart palpitations along with the itchiness going up along my neck now. And down the left trunk of my body. I'm feeling nausea at this point. I decide to lay down. By 8:45 my left arm, left neck, trunk , stomach area are itching beyond comfort levels , nausea is bad and heart palpitations are intense but no difficulty breathing. So I lay here thinking how absurd this is. My husband also had his second dose at the same time he was doing fine. So I take a Zofran for nausea and an antihistamine for the itch and a Ativan. I advise my husband of the situation so he's aware . In case of something worse prevails. I wake up in the morning feeling fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- Asthma
- Andere Medikamente
- Topamax, Sucralafate, Synthroid, Linzess,Zyrtec, Proton, Ativan ,Claritin, Magnesium , Lactaid, Gas X
- Allergien
- Latex, Banana, Strawberries, Wheat, Avocado, Celery, Pineapple, Apples Almonds,
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 19.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Injected limb mobility decreased
Injection site erythema
Injection site induration
Injection site pain
Injection site pruritus
Injection site swelling
Injection site warmth
Oedema peripheral
Pain
Rash macular
Tenderness
Vaccine positive rechallenge
Symptomtext
The injection site: Tender Large red spot splotchy Hot to touch Swollen Hard Itchy Other: Fever of 100.1 Chills Tenderness and swelling in left arm pit Pain in joints painful to lift arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Epilepsy Anxiety
- Vorgeschichte
- Epilepsy Anxiety
- Andere Medikamente
- Lamictal Keppra Hydroxyzine Buspar Vitamin D Omeprazole
- Allergien
- None
- Vorherige Impfungen
- Covid 19 modern dose 1 same adverse effects for second dose
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Hallucination
Urine analysis abnormal
Symptomtext
Patient reports having burning across her chest, hot urine, and hallucinations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 22.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Condition aggravated
Constipation
Decreased appetite
Fatigue
Headache
Hyperhidrosis
Hypersomnia
Pyrexia
Symptomtext
1st shot, 07/23/2021 woke up early in morning with chills, sweating, fever, severe headache, very weak, extremely tired. Pain in left arm at injection site with red, hot, hard area about 3" diameter, by the end of day, entire arm was red, hot, and very swollen to wrist. Itchy. Took 4 days for that to go away. Stayed in bed sleeping most of day and kept taking tylenol, and drinking water. I did not take any of my normal meds that day. Barely ate anything. 07/24/2021; Just rested most of day still tired and still severe headache, all other symptoms were gone except arm problem Headache took 3 days to go away fully. Has watery diarrhea 2X within 1 hour that day, then I was good. 2nd shot; felt good most of day, til 08/20/2021 at 1:30am. Had chills, Fever, even with 5 blankets and fully clothed with socks on for most of the night, Somewhere around 6am I woke up drenched in sweat, but still chills. I was very tired all day, headache but not as severe as 1st shot headache. Took tylenol all day (as soon as I got in my car to leave) with water as much as I could drink, to stay hydrated. Didn't really eat much. Constipated for 3 days this time. Slept for 18 hours. The next day still tired, rested all day sleeping about 12 hours. Next day good as new.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None, didnt even think of going for testing because i was pretty sure it was the side effects.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- Diabetes, Depression, Anxiety, Minor A-Fib
- Andere Medikamente
- Novalog, Tresiba, Carvedilol, Effexor, Wellbutrin, famotidine, Zyrtec, Tylenol
- Allergien
- I do have allergic reaction to something that comes on without warning. They have ran so many tests and still don't know why.
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 22.08.2021
- Impfdatum
- 18.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Decreased appetite
Dyspnoea
Fatigue
Headache
Hypersomnia
Pain
Peripheral coldness
Weight decreased
Symptomtext
I started to fell whole body side effect from 8/20/2021 around noon time. Symptoms are: headache, body ache, extremely tired, short breath, cold hands, no appetite, uncomfortable stomach. The symptoms got worse in the night. I slept about 15 hours and immediately lost 3 lbs. When I wake up at 10am on 8/21/2021, I had to take ibuprofen 2 pills and ionic zinc and forced myself to eat pasta + butter + fresh ginger to prevent further losing weight, and then I slept 3 hrs more. I gradually got better and better. I took another ibuprofen at maybe 3pm, in addition to Nettles, gingers, ionic zinc, green tea pills, etc. In the evening I felt a lot better so I did not take ibuprofen, but then I got almost all the symptoms back on 8/22 morning after slept almost 13 hours. Now I realize that I likely have to keep taking ibuprofen or Tylenol regularly to keep my symptoms controlled.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- N.A.
- Aktuelle Erkrankungen
- The one I am reporting here is my 2nd shot of Moderna vaccine (8/18/21). Actually after my first shot on 7/17/21, I was constantly felling tired for 3 weeks. Only the 4th week felt a bit normal.
- Vorgeschichte
- No.
- Andere Medikamente
- N.A.
- Allergien
- I did allergy test half year ago. The result shows that I am allergic to all the 40 environmental factors, but not allergic to any food that were tested. I kind of suspect this test because I knew I am allergic to some food, e.g. gluten, some type of peaches, etc.
- Vorherige Impfungen
- Felt very tired for 3 weeks after 1st shot.
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 22.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Condition aggravated
Diarrhoea
Dizziness
Extra dose administered
Headache
Injection site pain
Injection site swelling
Pain in extremity
Symptomtext
About 2 hours after receiving my Moderna Booster shot I was severely hit with Diarrhea for 28 hours. I took Imodium to help slow it down. It?s been about 40 hours now and my stomach is still upset. Also I still have pain at the injection site with a golf ball size lump that seems to be getting smaller now. During the second day my pain in the arm was really bad. It was a whole lot worse then when I received my second dose of Moderna. In fact it was almost triple the pain. I also experienced being a little dizzy and loopy the first day. These two symptoms were mild. I also have a faint headache that started about 20 hours after the Injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Complications breathing non COVID related. Went to ER got chest X-ray everything clear.
- Vorgeschichte
- Hashimoto?s disease, hypertension and obese bmi 38
- Andere Medikamente
- Lisinopril 10 -12 mcg hcr, Levothroxine 125 mcg, Vitamin D, Centrum Multivitamin, Tumeric Curcumin pills
- Allergien
- N/A
- Vorherige Impfungen
- Sore arm and headache, received Moderna second shot 4-1-21
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 18.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Mobility decreased
Pain in extremity
Peripheral swelling
Tenderness
Symptomtext
Patient came to the pharmacy on 8/18/21 @ 11:10am and said that the day after she received her Moderna vaccine in the left arm, her right arm started hurting and became swollen. She said she could not move her right arm therefore she said she went to her physician and her physician told her to take her gout medication at an increased dose. She said it lasted for about 5 days; the swelling went down but he arm was still a little tender.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 15.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Chest X-ray
Fatigue
Headache
Lymphadenopathy
Malaise
Pain
Pain in extremity
Palpitations
Pyrexia
Tachycardia
Symptomtext
8/11/21 Received 1st dose of Moderna Covid shot 8/12/21 Woke up at 4am for work and heart was racing, left arm hurting. Heart rate continued 140 beats at rest for over an hour. Went to ER. Diagnosed with tachycardia and lactate 2.2. I was seen by two emergency doctors (shift change) and both agreed it was possible symptom of the shot. Was given 2 bags of fluid. After receiving fluid my glands starting aching and had headache. Mid day at home had 101.1 fever. slept on and off rest of day. Drank fluids and switched between Tylenol and ibuprophen as instructed by ED doctors 8/13/21 Woke up at 2am with 102.6 fever, 120 heart rate, headache and aches. Again took tylenol, drank fluids. 8/14/21 Glands in neck are swollen, 99.5 low grade fever, headache, fatigue and just not feeling great. Tylenol and ibuprophen with drinking fluids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- 8/12/21 Blood work, telemetry, chest xray
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 12.04.2023
- Impfdatum
- 03.09.2021
- Beginn
- 06.04.2023
- Tage bis Beginn
- 580,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Blood culture negative
COVID-19
Chemotherapy
Chest X-ray normal
Early satiety
Gastric cancer
Immunosuppression
Laboratory test abnormal
Lymphoma
Neutropenia
Pancytopenia
Pyrexia
Rhinovirus infection
SARS-CoV-2 test positive
Weight decreased
Symptomtext
Brief Summary of Hospital Stay: Patient is under treatment for Large cell lymphoma, extranodal and solid organ sites with Malignant neoplasm of overlapping sites of stomach leading to chronic Epigastric pain, Early satiety, Weight loss. On routine lab testing he was found to have Pancytopenia due to antineoplastic chemotherapy, including Chemotherapy induced neutropenia. He had a very low grade fever so was instructed to come to the hospital. He was found have both COVID-19 and Rhinovirus infections. He is not dyspneic or hypoxic. No acute findings on chest film. In addition to neutropenia, he has further immunosuppression as he is On prednisone therapy so completred three day course of REMDESIVIR. He was also empirically started on VANCOMYCIN and CEFEPIME but blood cultures were negative at 72 hours so antibiotics discontinued. Oncology recommended starting FILGRASTIM and his ANC rose to 1500 prior to discharge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- 4,0
- Labordaten
- COVID positive PCR 4/6/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 22.01.2023
- Impfdatum
- 28.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Gait inability
Joint swelling
Symptomtext
Unable to walk from excruciating joint swelling and inflammation in knees, ankles, and hips lasting for 2-3 days with reoccurring ?flare ups? of excruciating knee, ankle, hip pain ever since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- Mild hypertension
- Andere Medikamente
- Amlodipine 5mg and Kariva (birth control)
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 12.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Biopsy skin abnormal
Blood test
Chills
Cutaneous vasculitis
Headache
Joint swelling
Muscle spasms
Oropharyngeal pain
Pain
Peripheral swelling
Rash
Rash erythematous
Vomiting
Symptomtext
8/12/2021- about 4 hours after vaccine started with headache, chills, body started hurting, then I went to bed and all through the night I was sick to my stomach and got a vest bad sore throat. Ankles started to have swollen into them. 9/10/2021- Started throwing up a few hours after with pains in my stomach and swelling of my legs again and now my hands as well. Red dots start on my legs and would come and go blow my knees. 2/11/2022- After the booster I ended up with swelling of my hands and feet. Little red dots on my legs would come and go way more than I got on my legs after 2nd shot Started with a lot of cramping in my toes and very bad headaches worse then i have ever had in my life
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- A lot of blood work from 2021 until now. Also had a biopsy says red dots are Leukocytoclastic vasculitis. and since the vaccine my blood has changed more then ever
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- mango and aloe
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 19.09.2022
- Impfdatum
- 14.09.2021
- Beginn
- 25.08.2022
- Tage bis Beginn
- 345,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest discomfort
Cough
Fatigue
Headache
Oropharyngeal pain
Productive cough
Pyrexia
SARS-CoV-2 test positive
Sleep disorder
Symptomtext
Towards Thursday afternoon I started experiencing a sore throat. About 3:00AM on Friday, I had a slight fever and a headache which awakened me. I took a COVID-19 home test and got a faint positive. The fever continued to about 100.0 I developed some fatigue and a yucky cough. I started to feel a little discomfort in my upper chest so I made an appointment and saw the doctor on that Saturday. I had a fever of 101.1, I had taken a 2nd test on Friday and it immediately was positive. I took a total of 3 test and all were positive. I was prescribed PAXLOVID and all my symptoms improved except for the cough. I still have coughs that produces phlegm 2 or 3 times an hour that I did not have prior to this. My fatigue subsided about 7 or 8 days ago.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test-August 26th and 27th 2022-positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HIV; Diabetic
- Andere Medikamente
- Vitamin D; FLONASE; TIVICAY; abacavir-lamivudine; CIALIS; albuterol rescue inhaler
- Allergien
- Ciclosporin; doxycycline monohydrate; shellfish
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 23.08.2022
- Impfdatum
- 21.08.2021
- Beginn
- 15.02.2022
- Tage bis Beginn
- 178,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Fatigue
Pain in extremity
Pyrexia
SARS-CoV-2 test positive
Symptomtext
After the vaccine I experience soreness on my arm for a few days. The fatigues came gradually, more than usual and it seems to get worst over time, I woke up tired and at the end of the day I was more tired. I addressed the problem with the doctor, and he did different test works. I will check with my Cardiologist, I have tried different supplement to boost my system, but it does not seems to work. I tested negative on a home test COVID-19 but on August 18th, 2022 I tested positive; I had fever for three days and I have extreme fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- August 17 COVID-19 negative; August 18 COVID-19 positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Cholesterol
- Andere Medikamente
- Levothyroxine; MITOQ; DEPLIN; nutritional supplements
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 11.06.2022
- Impfdatum
- 01.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 15,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash erythematous
Rash papular
Urticaria
Symptomtext
RASH/hives raised reddened area, itchy. Have multiple photos
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Did not have any
- Aktuelle Erkrankungen
- Chronic pain, situational tachycardia
- Vorgeschichte
- Chronic pain from 4 back surgeries
- Andere Medikamente
- Oxycodone, morphine, gabapentin, flexaril, Metoprolol
- Allergien
- Latex, droperidol
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 21.05.2022
- Impfdatum
- 30.09.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 42,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Carbohydrate antigen 125
Feeling abnormal
Inappropriate schedule of product administration
Malaise
Ovarian cancer stage IV
Vaccination site pain
Weight
Symptomtext
diagnosed with ovarian peritoneal cancer; she doesn't feel well but doesn't know if that feeling is due to the cancer or chemotherapy; felt yucky; first two doses of the Moderna COVID-19 vaccine on 30SEP2021 and 11NOV2021; had arm pain after 2nd dose; This spontaneous case was reported by a consumer and describes the occurrence of OVARIAN CANCER STAGE IV (diagnosed with ovarian peritoneal cancer) in an 81-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 039F21A and 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Patient was not tested/diagnosed positive for COVID-19. Concurrent medical conditions included Penicillin allergy, Allergy to antibiotic (allergic to Keflex), Allergy to chemicals (Allergic to Sulfur) and Chemical sensitivity (environmental sensitivity to different chemicals). Concomitant products included COLECALCIFEROL (VITAMIN D3), ZINC PICOLINATE, MAGNESIUM L-THREONATE (MAGTEIN), MAGNESIUM TAURATE, MAGNESIUM GLYCINATE and FYTATE CALCIUM MAGNESIUM (CELL FORTE IP-6 & INOSITOL) for an unknown indication. On 30-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 11-Nov-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to .5 milliliter. On 11-Nov-2021, the patient experienced VACCINATION SITE PAIN (had arm pain after 2nd dose) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first two doses of the Moderna COVID-19 vaccine on 30SEP2021 and 11NOV2021). On 12-Nov-2021, the patient experienced FEELING ABNORMAL (felt yucky). In February 2022, the patient experienced OVARIAN CANCER STAGE IV (diagnosed with ovarian peritoneal cancer) (seriousness criteria hospitalization and medically significant). On an unknown date, the patient experienced MALAISE (she doesn't feel well but doesn't know if that feeling is due to the cancer or chemotherapy). The patient was hospitalized from 17-Feb-2022 to 01-Mar-2022 due to OVARIAN CANCER STAGE IV. The patient was treated with CARBOPLATIN for Ovarian cancer, at an unspecified dose and frequency; LIDOCAINE (LIDOCAIN [LIDOCAINE]) for Cancer pain and Postoperative pain, at an unspecified dose and frequency; IBUPROFEN (MOTRIN [IBUPROFEN]) for Cancer pain and Postoperative pain, at an unspecified dose and frequency; PACLITAXEL (TAXOL) for Ovarian cancer, at an unspecified dose and frequency and Surgery for Ovarian cancer stage IV. On 16-Nov-2021, VACCINATION SITE PAIN (had arm pain after 2nd dose) and FEELING ABNORMAL (felt yucky) had resolved. At the time of the report, OVARIAN CANCER STAGE IV (diagnosed with ovarian peritoneal cancer) had not resolved and MALAISE (she doesn't feel well but doesn't know if that feeling is due to the cancer or chemotherapy) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first two doses of the Moderna COVID-19 vaccine on 30SEP2021 and 11NOV2021) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In October 2021, Weight: lost 18 pounds lost 18 pounds since fall 2021. In February 2022, Carbohydrate antigen 125: 1125 1125. On an unknown date, Carbohydrate antigen 125: 99 99, 19 19 and 8 8. Concomitant medications included high dosage probiotic. Patient was diagnosed with stage 4, Ovarian peritoneal cancer in Feb 2022. Patient said that she probably had the cancer for a while, but it was diagnosed more recently. Patient was hospitalized on17-Feb-2022 for surgery of ovarian cancer, patient had an incision going from under her heart to the bladder. Patient had a major surgery for the cancer in Feb2022 and was getting infusions to treat the cancer. She had received 2 infusions and would be getting a 3rd one in 2 weeks. Patient said that the chemotherapy she was receiving with Taxol and Carboplatin was working well because her CA-125 marker has decreased significantly since she started the infusions. Her CA-125 was 1125 in Feb 2022. Before she started chemotherapy, it fell to 99 and the last two times it fell even more to 19 and 8, respectively. She also stated that she had arm pain after the 1st and 2nd dose of the Moderna COVID-19 vaccine. The pain lasted for 4-5 days. She received the shots on her right arm but couldn't remember which arm experienced the pain. She also felt yucky for 2 to 3 days after receiving both doses of the Moderna vaccine. She stated that she had lost 18 lbs since fall 2021. Treatment medications included Homeopathic T-relief for pain associated with the cancer surgery and/or the disease itself. Caller wanted to know if she could receive the full dose for her 3rd dose or half dose of Moderna. She also wanted to know if there were any potential interactions between her chemotherapy treatment and the Moderna vaccine. Company comment: This spontaneous case concerns an 81-year-old, female patient with no reported relevant medical history, who experienced the unexpected, serious (hospitalized, medically significant) event of Ovarian cancer stage IV, with non-serious event of Malaise. Inappropriate schedule of product administration was reported as an additional event wherein the patient received mRNA-1273 as primary series with dosing interval of 42 days - not within the recommended window period. Other non-serious events were also experienced immediately after vaccination and were reported resolved within a week post-vaccination. The serious event was diagnosed approximately 3 months after receiving the second dose of mRNA-1273, with CA-125 value of 1125; although the patient already observed weight loss even prior to diagnosis. Other presenting symptoms with onset dates were not provided in the case. The patient underwent an unspecified surgery after diagnosis and is now receiving chemotherapy with Taxol and Carboplatin, with note of improving tumor marker after initiation of treatment. The elderly age of the patient could be considered a risk factor for the gynecologic malignancy. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to MOD-2022-568750.; Sender's Comments: This spontaneous case concerns an 81-year-old, female patient with no reported relevant medical history, who experienced the unexpected, serious (hospitalized, medically significant) event of Ovarian cancer stage IV, with non-serious event of Malaise. Inappropriate schedule of product administration was reported as an additional event wherein the patient received mRNA-1273 as primary series with dosing interval of 42 days - not within the recommended window period. Other non-serious events were also experienced immediately after vaccination and were reported resolved within a week post-vaccination. The serious event was diagnosed approximately 3 months after receiving the second dose of mRNA-1273, with CA-125 value of 1125; although the patient already observed weight loss even prior to diagnosis. Other presenting symptoms with onset dates were not provided in the case. The patient underwent an unspecified surgery after diagnosis and is now receiving chemotherapy with Taxol and Carboplatin, with note of improving tumor marker after initiation of treatment. The elderly age of the patient could be considered a risk factor for the gynecologic malignancy. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 13,0
- Labordaten
- Test Name: CA 125; Result Unstructured Data: 99; Test Name: CA 125; Result Unstructured Data: 19; Test Name: CA 125; Result Unstructured Data: 8; Test Date: 202202; Test Name: CA 125; Result Unstructured Data: 1125; Test Date: 202110; Test Name: weight; Result Unstructured Data: lost 18 pounds since fall 2021
- Aktuelle Erkrankungen
- Allergy to antibiotic (allergic to Keflex); Allergy to chemicals (Allergic to Sulfur); Chemical sensitivity (environmental sensitivity to different chemicals); Penicillin allergy
- Vorgeschichte
- Comments: Patient was not tested/diagnosed positive for COVID-19.
- Andere Medikamente
- VITAMIN D3; ZINC PICOLINATE; MAGTEIN; MAGNESIUM TAURATE; MAGNESIUM GLYCINATE; CELL FORTE IP-6 & INOSITOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Pain in extremity
Weight
Symptomtext
felt yucky for 2 to 3 days; had arm pain that lasted for 4 to 5 days; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (felt yucky for 2 to 3 days) and PAIN IN EXTREMITY (had arm pain that lasted for 4 to 5 days) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. The patient had never been diagnosed or tested positive for COVID-19. No other vaccines were given to the patient within 1 month prior to Moderna COVID-19 vaccine. Concurrent medical conditions included Ovarian cancer stage IV (had the Ovarian peritoneal cancer for a while but it was diagnosed more recently in Feb-2022), Penicillin allergy, Allergy to antibiotic (Keflex allergy), Drug allergy (Sulfur allergy) and Allergy to chemicals (environmental sensitivity to different chemicals). Concomitant products included PACLITAXEL (TAXOL) and CARBOPLATIN for Ovarian cancer, COLECALCIFEROL (VITAMIN D3), IP-6, INOSITOL, ZINC PICOLINATE, MAGNESIUM L-THREONATE (MAGTEIN), MAGNESIUM TAURATE and MAGNESIUM GLYCINATE for an unknown indication. On 30-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 30-Sep-2021, the patient experienced PAIN IN EXTREMITY (had arm pain that lasted for 4 to 5 days). On 01-Oct-2021, the patient experienced FEELING ABNORMAL (felt yucky for 2 to 3 days). In October 2021, FEELING ABNORMAL (felt yucky for 2 to 3 days) and PAIN IN EXTREMITY (had arm pain that lasted for 4 to 5 days) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, Weight: lost 18 pounds (Low) had lost 18 pounds since the fall of 2021. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. Concomitant medications also included high dosage probiotic and IP-6 inositol. Treatment information was not reported for events that occurred after first dose vaccination. This case was linked to MOD-2022-568683 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: Weight; Result Unstructured Data: had lost 18 pounds since the fall of 2021
- Aktuelle Erkrankungen
- Allergy to antibiotic (Keflex allergy); Allergy to chemicals (environmental sensitivity to different chemicals); Drug allergy (Sulfur allergy); Ovarian cancer stage IV (had the Ovarian peritoneal cancer for a while but it was diagnosed more recently in Feb-2022); Penicillin allergy
- Vorgeschichte
- Comments: The patient had never been diagnosed or tested positive for COVID-19. No other vaccines were given to the patient within 1 month prior to Moderna COVID-19 vaccine.
- Andere Medikamente
- VITAMIN D3; IP-6; INOSITOL; ZINC PICOLINATE; MAGTEIN; MAGNESIUM TAURATE; MAGNESIUM GLYCINATE; TAXOL; CARBOPLATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Lymphadenopathy
Pyrexia
Symptomtext
Swelling of lymph nodes under left arm pit for four or five days and I ran a fever plus I felt weird
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- No.
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- Asthma
- Andere Medikamente
- Citracal D3 Viotin D3 Turmeric
- Allergien
- No.
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 16.08.2021
- Beginn
- 18.03.2022
- Tage bis Beginn
- 214,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Cough
Diarrhoea
Fatigue
Gastroenteritis viral
Headache
Malaise
Oropharyngeal pain
SARS-CoV-2 test positive
Vertigo
Symptomtext
On the 16th of March I got a fusion of COVID antibodies Evusheild at the hospital, 2 days before I started getting sick. I started coughing, had diarrhea, sore throat and felt really sick, weak and tired. I had headache for a couple of days with really bad vertigo. And stomach.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- I did a COVID test on the 23th - positive; 28th COVID home test - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Regeners autoimmune disease
- Andere Medikamente
- Atobaquone, Zereloto, Folic Acid, Omeprozole, B complex, Benadryl, Tylenol. I'm given rituximab every 6 months to knock out my immune system (november and may)
- Allergien
- Codeine; Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 13.03.2022
- Impfdatum
- 28.08.2021
- Beginn
- 29.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Chills
Fatigue
Nausea
Pain in extremity
Pyrexia
Rash
Symptomtext
Fever, chills, tired, dizziness, sore armpit, nauseous, sore arm, and rash on arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seasonal allergies, anxiety/depression, migraines
- Andere Medikamente
- Claritin D, topiramate, Prozac
- Allergien
- Codeine
- Vorherige Impfungen
- Can't get a TB skin test because I test positive, have to get the chest x-ray
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 02.09.2021
- Beginn
- 12.02.2022
- Tage bis Beginn
- 163,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Hypersensitivity
Pain
Pain in extremity
Rash
Urticaria
Symptomtext
4 weeks after the shot I experienced an allergic reaction to Prednisone which caused to me to break out into hives all over my body. On 2/12 I started getting a weird pain on my right-hand side. By Saturday, I developed a patchy and very painful rash starting from my right breast to my back. On Sunday I went to the doctor and they diagnosed me w/ shingles and gave me a shot and put me on Valtrex which dried the rash up in 3 days but the pain persisted. I went to my PCP a few days later and was prescribed Gabapentin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Tamoxifen
- Allergien
- Excedrin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- 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
Headache
Inappropriate schedule of product administration
Pain in extremity
Peripheral swelling
Pyrexia
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of PAIN IN EXTREMITY (sore arm), PERIPHERAL SWELLING (arm swelling), PYREXIA (fever), HEADACHE (headache) and EXPIRED PRODUCT ADMINISTERED (Patient received expired 2nd dose) in a 54-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 23-Feb-2022, the patient received second dose of mRNA-1273 (Spikevax) (Intramuscular) .5 milliliter. On 23-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received expired 2nd dose) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (more than 35 days between first and second dose). On an unknown date, the patient experienced PAIN IN EXTREMITY (sore arm), PERIPHERAL SWELLING (arm swelling), PYREXIA (fever) and HEADACHE (headache). At the time of the report, PAIN IN EXTREMITY (sore arm), PERIPHERAL SWELLING (arm swelling), PYREXIA (fever), HEADACHE (headache), EXPIRED PRODUCT ADMINISTERED (Patient received expired 2nd dose) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (more than 35 days between first and second dose) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. Treatment information was not provided. On 30-Nov-2021, the patient received first dose of Moderna (Intramuscular) .5 milliliter. Batch number was the same as second dose, 049E21A. It was reported that the patient did not want to get the second dose but was eventually forced to get the second dose by her employer. This case was linked to MOD-2022-501302 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 11.05.2021
- Beginn
- 25.02.2022
- Tage bis Beginn
- 290,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Acute kidney injury
Anion gap
Asthenia
Blood bicarbonate decreased
Blood creatinine increased
Blood potassium decreased
Blood sodium decreased
Blood urea increased
COVID-19
Chills
Computerised tomogram abdomen normal
Cough
Decreased appetite
Diabetic ketoacidosis
Diarrhoea
Discomfort
Fatigue
Symptomtext
Patient presents to the emergency department with complaint of worsening cough, diarrhea, and weakness over the last 7 to 10 days. Patient states she had a positive Covid test on Monday, symptoms are getting worse. Patient is worried as she does have a kidney transplant and does not want to get "dehydrated". Patient complains of diffuse abdominal achiness, nonradiating, associated with nausea and vomiting. Patient has generalized body aches and weakness. Patient rates discomfort 5 out of 10. Patient does admit to nausea with some episodes of vomiting. Patient has large amount of diarrhea, nonbloody. This patient is a pleasant 53-year-old female with past medical history of diabetes mellitus dependent on insulin, hypertension, end-stage renal disease status post kidney transplant about 45 years ago who is following up with a local nephrologist, on CellCept, tacrolimus, and prednisone. She lives with her husband. She is active tobacco smoker, denies abnormal alcohol use or illicit drug use.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 3,0
- Labordaten
- Patient presented to the ER for evaluation of intractable nausea and vomiting and was worried she is getting dehydrated. Her symptoms started about 3 weeks ago, tested positive for COVID-19 on 2/14/2022. She reported worsening cough, fatigue, nausea and vomiting. She also reported diarrhea which is described as loose stool. She did have some chills but not consistent. She has poor appetite and not able to keep food down. She use insulin for diabetes however she did stop taking her insulin for few days because she was worried about hypoglycemia. She did not take her blood pressure medication last night because she was worried she is getting dehydrated and hypotensive. Patient is vaccinated for COVID-19 with booster dose. She is active tobacco smoker however she did not smoke for the past week because it worsened the nausea. ER course: Patient was awake, alert, oriented, in no acute distress. Her labs revealed acute kidney injury with creatinine of 5.4, BUN of 56. She also has sodium of 118, potassium 3.0, bicarb of 10 and anion gap of 17. CT scan of the abdomen was obtained because of kidney injury did not reveal evidence of obstruction. ER provider did contact her nephrologist and recommended management with hydration for now and monitor kidney function. Patient is admitted for moderate DKA with hypokalemia and hyponatremia. Patient started on IV fluid resuscitation. Or COVID-19 infection patient will be on IV antibiotics and steroid.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Kidney transplant/ CRF DM HTN IBS
- Andere Medikamente
- Current Home Medications 1. ALPRAZolam 0.5 mg oral tablet, extended release : 1 tab(s) orally 3 times a day, As Needed - PRN for Anxiety 2. glucagon 1 mg injection : null 3. Lantus 100 units/mL subcutaneous solution : 10 unit(s) subcutaneou
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 18.08.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 89,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy
Blood test
Cellulitis
Erythema
Lyme disease
Rash
Symptomtext
On Nov 15th my rheumatoid Dr. drew my blood. I noticed a red spot that lingered for a few days. I saw my PCP and they treated me for cellulitis and treated it for several things and didn't get better. Send me to another dermatologist on 12/16 and they tested me and it confirmed Lyme disease. After a week of treatment the rash went away but I'm still testing positive for Lyme disease.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Standard blood work and biopsy of the arm, positive for Lyme disease.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- I have rheumatoid arthritis; diabetic; high blood pressure
- Andere Medikamente
- Methotrexate; Humira; prednisone; folic acid; ibandronate; vit d2; vitamin c; methenamine; atenolol; potassium; metolazone; spironolactone. Bumetanide; Singulair; rosuvastatin; gabapentin; aspirin; Zyrtec; magnesium; Jardiance; daily shot H
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 18.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Pyrexia
Symptomtext
Approximately a few hours after my vaccination I experienced the following: Fever, Chills, Fatigue and this lasted for about 72 hours. I took TYLENOL to suppress the symptoms and I felt better the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Multiple scoliosis
- Andere Medikamente
- OCREVUS
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 28.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blood cholesterol normal
Blood electrolytes normal
Blood glucose normal
Blood iron normal
Bronchial wall thickening
Bronchitis
Chest X-ray abnormal
Chills
Dizziness
Fatigue
Glycosylated haemoglobin increased
Inflammatory marker test
Laboratory test normal
Liver function test normal
Mononucleosis heterophile test negative
Mycobacterium tuberculosis complex test negative
Renal function test normal
Rheumatoid factor negative
Symptomtext
Chills, fatigue, and dizziness since three days after the second dose of Moderna. Has not gone away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 10/21/21 to present: Labs to include checking - autoimmune issues, mono, blood sugar, anemia, electrolytes, kidney function, liver function, cholesterol, thyroid, inflammation, iron, tuberculosis, rheumatoid arthritis - all negative except blood sugar was high(A1C 7.4). Chest x-ray indicated bronchial wall thickening - treated as bronchitis with Z-pac; no change.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, diabetes, arthritis, high blood pressure, & high cholestrol
- Andere Medikamente
- Adderall XR 20 mg / Albuterol 90 mcg(inhaler) / Allopurinol 100 mg / Lisinopril 10 mg / Montelukast 10 mg / Alvesco 80 mcg (inhaler) / Metoprolol 25 mg / Rosuvastatin 40 mg / Metformin 500 mg 2 X daily / Baby aspirin 81 mg / Men's multivit
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 01.05.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 123,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Influenza like illness
Interchange of vaccine products
Neutrophil count
Neutrophil count decreased
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of NEUTROPHIL COUNT DECREASED (Neutrophils have been at critically low levels/low blood count situation), INFLUENZA LIKE ILLNESS (Light flu like symptoms), FATIGUE (Fatigue) and INTERCHANGE OF VACCINE PRODUCTS (received the Janssen COVID-19 vaccine and then received two doses of the Moderna COVID-19 vaccine) in a 54-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 062E21A and 049E21A) for COVID-19 vaccination. Co-suspect product included non-company product VALACICLOVIR for Shingles.Previously administered products included for COVID-19 vaccination: Janssen covid 19 vaccine on 14-Mar-2021. Past adverse reactions to the above products included No adverse event with Janssen covid 19 vaccine.Concurrent medical conditions included Lymphoma (She was in remission and not took any treatments for the lymphoma.) and Shingles (Because she still has the infection, she has been on the antiviral treatment since May2021) since May 2021.Concomitant products included MULTIVITAMINS [VITAMINS NOS] and VITAMIN D [VITAMIN D NOS] for an unknown indication. In May 2021, the patient VALACICLOVIR (unknown route) dosage was changed to at an unspecified dose.On 12-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form.On 09-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient started VALACICLOVIR (unknown route) at an unspecified dose. In 2021, the patient experienced NEUTROPHIL COUNT DECREASED (Neutrophils have been at critically low levels/low blood count situation). On 09-Sep-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (received the Janssen COVID-19 vaccine and then received two doses of the Moderna COVID-19 vaccine). In September 2021, the patient experienced INFLUENZA LIKE ILLNESS (Light flu like symptoms) and FATIGUE (Fatigue). On 09-Sep-2021, INTERCHANGE OF VACCINE PRODUCTS (received the Janssen COVID-19 vaccine and then received two doses of the Moderna COVID-19 vaccine) had resolved. In September 2021, INFLUENZA LIKE ILLNESS (Light flu like symptoms) and FATIGUE (Fatigue) had resolved. At the time of the report, NEUTROPHIL COUNT DECREASED (Neutrophils have been at critically low levels/low blood count situation) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available):In January 2021, Neutrophil count: normal (normal) Normal.In April 2021, Neutrophil count: normal (normal) Normal.In 2021, Neutrophil count: low (Low) critically low levels. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments.No treatment medications were reported.The patient received the Moderna vaccine in August and September 2021. Since that time, her neutrophils have been at critically low levels. The root cause of this drop in neutrophils (they were normal during routine checks in January and April of this year) was not established. The patient also had some fatigue and light flu-like symptoms after receiving both doses. Those symptoms lasted for approximately 24 hours, but she says it was nothing major. She reported that after receiving the second dose of the Moderna vaccine, her neutrophil count had been very low. She mentioned that she has a history of chronic lymphoma for which she has been treated in the past. She was currently in remission and was not going through any treatments for the lymphoma. She sees an Oncologist and Hematologist for regular checkups. She was diagnosed with Shingles in May 2021 for which she was put on Valcyclovir. Because she still has the infection, she has been on the antiviral treatment since May 2021. She stopped taking the shingles treatment to see if it would make a difference in her neutrophil count, but nothing happened for 2 weeks after stopping the medication and her neutrophil count was still low. She then decided to restart the Valcyclovir treatment. She was trying to figure out the reason for the low neutrophil count and wants to know if there is any data which points to the Moderna vaccine as the cause.This case was linked to MOD-2021-422103 (Patient Link).Most recent FOLLOW-UP information incorporated above includes:On 20-Dec-2021: Non-significant Follow up information received: I narrative updated.On 21-Dec-2021: Significant Follow up received: Events (fatigue and light flu like symptoms), medical history (Shingles and lymphoma), historical vaccine, Co-suspect and concomitant medications added. I narrative updated.; Sender's Comments: This case concerns a 54-year-old female patient with medical history of chronic lymphoma (currently in remission, as stated). After administration of the second dose of the mRNA-1273 vaccine, the patient experienced non-serious unexpected events of Neutrophil count decreased and Influenza like illness, as well as non-serious expected event of Fatigue. The events of Fatigue and Influenza like illness lasted only 24 hours and then resolved without any treatment. However, the patient developed very low neutrophil count after this second dose that was still ongoing at the time of this report (laboratory findings with reference ranges were not provided). Co-suspect medication Valaciclovir which was used for the treatment of Herpes zoster infection remains a significant confounding factor for this event. In addition, underlying lymphoma is considered as an additional significant confounding factor for this event. The re-challenge for the events of Fatigue and Influenza like illness could have been considered positive, having in mind that it was confirmed that the patient developed these events after the first dose, as well. The benefit-risk relationship of the mRNA-1273 vaccine is not affected by this report. Event seriousness assessed as per Regulatory Authority reporting. Having in mind that this patient received the Janssen COVID-19 vaccine prior to vaccination with the company product, Interchange of vaccine products should have been considered in this specific case. The company causality for this event is not applicable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 202101; Test Name: Neutrophil count; Result Unstructured Data: Normal; Test Date: 202104; Test Name: Neutrophil count; Result Unstructured Data: Normal; Test Date: 2021; Test Name: Neutrophil count; Result Unstructured Data: critically low levels.
- Aktuelle Erkrankungen
- Lymphoma (She was in remission and not took any treatments for the lymphoma.); Shingles (Because she still has the infection, she has been on the antiviral treatment since May2021.)
- Vorgeschichte
- -
- Andere Medikamente
- MULTIVITAMINS [VITAMINS NOS]; VITAMIN D [VITAMIN D NOS.]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 24.12.2021
- Impfdatum
- 12.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Influenza like illness
Symptomtext
light flu like symptoms; fatigue; This spontaneous case was reported by a consumer and describes the occurrence of INFLUENZA LIKE ILLNESS (light flu like symptoms) and FATIGUE (fatigue) in a 54-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Janssen COVID-19 vaccine on 14-Mar-2021. Past adverse reactions to the above products included No adverse event with Janssen COVID-19 vaccine. Concurrent medical conditions included Lymphoma (treated in the past. She is currently in remission and is not going through any treatments) and Shingles (Patient put on Valcyclovir.) since May 2021. Concomitant products included VALACICLOVIR HYDROCHLORIDE (VALCYVIR) for Shingles, MULTIVITAMIN [VITAMINS NOS] and VITAMIN D NOS for an unknown indication. On 12-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Aug-2021, the patient experienced INFLUENZA LIKE ILLNESS (light flu like symptoms) and FATIGUE (fatigue). On 13-Aug-2021, INFLUENZA LIKE ILLNESS (light flu like symptoms) and FATIGUE (fatigue) had resolved. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No treatment drugs were reported. This case was linked to MOD-2021-418874 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Lymphoma (treated in the past. She is currently in remission and is not going through any treatments); Shingles (Patient put on Valacyclovir.)
- Vorgeschichte
- -
- Andere Medikamente
- MULTIVITAMIN [VITAMINS NOS]; VITAMIN D NOS; VALCIVIR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 08.09.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 37,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Gait disturbance
Magnetic resonance imaging
Symptomtext
On 10/15/2021, I started to have serve pain in my lower back, that completely crippled me to where I could barely walk. This lasted for about two days. Since then, I have repeated off and on of the same symptoms, once a week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- 12/02/2021 - MRI
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure, Pre-diabetic, Thyroid issue, Chronic back pain
- Andere Medikamente
- Synthroid 275mg, Toprol XL 200mg, Procardia XL 60mg, Dyazide 25mg, Crestor 5mg, Niacin 500mg, Neurontin 600mg 3 times a day, Metformin HCL 500mg 2x/day, Omega3 2 capsules 2x/day, OxyContin ER 30mg every 12 hours.
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Pain in extremity
Vaccination complication
Symptomtext
term expired vials were used to provide 38 doses; Sore arm; some identified common side effects after the vaccine (ex: sore arm, etc.); This spontaneous case was reported by an other health care professional and describes the occurrence of PAIN IN EXTREMITY (Sore arm), VACCINATION COMPLICATION (some identified common side effects after the vaccine (ex: sore arm, etc.) ) and EXPIRED PRODUCT ADMINISTERED (term expired vials were used to provide 38 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (term expired vials were used to provide 38 doses). In November 2021, the patient experienced PAIN IN EXTREMITY (Sore arm) and VACCINATION COMPLICATION (some identified common side effects after the vaccine (ex: sore arm, etc.) ). On 01-Nov-2021, EXPIRED PRODUCT ADMINISTERED (term expired vials were used to provide 38 doses) had resolved. In November 2021, PAIN IN EXTREMITY (Sore arm) and VACCINATION COMPLICATION (some identified common side effects after the vaccine (ex: sore arm, etc.) ) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. No vial went any temperature excursions. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. Till 19-Nov-2021, there were no adverse reactions to the vaccine. As of 19 Nov 2021, there were no adverse reactions to the vaccine reported by the list below. We spoke with some that received the vaccine during these dates and some identified common side effects after the vaccine (ex: sore arm, etc.) and only lasted for a few hours but no more than 24 hours for 1st dose, 2nd dose and Booster. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 18-Nov-2021: The additional information included suspect administration date. On 19-Nov-2021: Follow-up information included about patients details On 19-Nov-2021: Significant FU appended (Second reporter Information was updated)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Vaccination complication
Vaccination site pain
Symptomtext
expired vials were used to provide 38 doses; Sore arm; some identified common side effects after the vaccine (ex: sore arm, etc.); This spontaneous case was reported by an other health care professional and describes the occurrence of VACCINATION COMPLICATION (some identified common side effects after the vaccine (ex: sore arm, etc.) ), EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) and VACCINATION SITE PAIN (Sore arm) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) and VACCINATION SITE PAIN (Sore arm). In November 2021, the patient experienced VACCINATION COMPLICATION (some identified common side effects after the vaccine (ex: sore arm, etc.) ). On 01-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) and VACCINATION SITE PAIN (Sore arm) had resolved. In November 2021, VACCINATION COMPLICATION (some identified common side effects after the vaccine (ex: sore arm, etc.) ) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. No vial went any temperature excursions. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. Till 19-Nov-2021, there were no adverse reactions to the vaccine. As of 19 Nov 2021, there were no adverse reactions to the vaccine reported by the list below. We spoke with some that received the vaccine during these dates and some identified common side effects after the vaccine (ex: sore arm, etc.) and only lasted for a few hours but no more than 24 hours for 1st dose, 2nd dose and Booster. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 18-Nov-2021: The additional information included suspect administration date. On 19-Nov-2021: Follow-up information included about patients details On 19-Nov-2021: Significant FU appended (Second reporter Information was updated)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Pain in extremity
Vaccination complication
Symptomtext
expired vials were used to provide 38 doses; Sore arm; some identified common side effects after the vaccine (ex: sore arm, etc.); This spontaneous case was reported by an other health care professional and describes the occurrence of PAIN IN EXTREMITY (Sore arm), VACCINATION COMPLICATION (some identified common side effects after the vaccine (ex: sore arm, etc.)) and EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses). In November 2021, the patient experienced PAIN IN EXTREMITY (Sore arm) and VACCINATION COMPLICATION (some identified common side effects after the vaccine (ex: sore arm, etc.)). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) had resolved. In November 2021, PAIN IN EXTREMITY (Sore arm) and VACCINATION COMPLICATION (some identified common side effects after the vaccine (ex: sore arm, etc.)) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. No vial went any temperature excursions. On 12-Nov-2021, all vaccines were administered within 2 hours. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. Till 19-Nov-2021, there were no adverse reactions to the vaccine. As of 19 Nov 2021, there were no adverse reactions to the vaccine reported by the list below. We spoke with some that received the vaccine during these dates and some identified common side effects after the vaccine (ex: sore arm, etc.) and only lasted for a few hours but no more than 24 hours for 1st dose, 2nd dose and Booster. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 18-Nov-2021: The additional information included suspect administration date. On 19-Nov-2021: Non-Significant Follow Up Appended : Second reporter Information was updated On 19-Nov-2021: Significant FU appended (Second reporter Information was updated)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Pain in extremity
Vaccination complication
Symptomtext
Expired vials were used to provide 38 doses of the Moderna Covid-19 Vaccine; Sore arm; Some identified common side effects after the vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vials were used to provide 38 doses of the Moderna Covid-19 Vaccine), PAIN IN EXTREMITY (Sore arm) and VACCINATION COMPLICATION (Some identified common side effects after the vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vials were used to provide 38 doses of the Moderna Covid-19 Vaccine). In November 2021, the patient experienced PAIN IN EXTREMITY (Sore arm) and VACCINATION COMPLICATION (Some identified common side effects after the vaccine). On 05-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vials were used to provide 38 doses of the Moderna Covid-19 Vaccine) had resolved. In November 2021, PAIN IN EXTREMITY (Sore arm) and VACCINATION COMPLICATION (Some identified common side effects after the vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment medications were provided Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. No vial went any temperature excursions. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Non significant follow up received on 19-nov-2021 and new reporter information added
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Pain in extremity
Vaccination complication
Symptomtext
expired vials were used to provide 38 doses; Sore arm; some identified common side effects after the vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses), PAIN IN EXTREMITY (Sore arm) and VACCINATION COMPLICATION (some identified common side effects after the vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses). In November 2021, the patient experienced PAIN IN EXTREMITY (Sore arm) and VACCINATION COMPLICATION (some identified common side effects after the vaccine). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) had resolved. In November 2021, PAIN IN EXTREMITY (Sore arm) and VACCINATION COMPLICATION (some identified common side effects after the vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. No vial went any temperature excursions. On 12-Nov-2021, all vaccines were administered within 2 hours. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. Till 19-Nov-2021, there were no adverse reactions to the vaccine. As of 19 Nov 2021, there were no adverse reactions to the vaccine reported by the list below. We spoke with some that received the vaccine during these dates and some identified common side effects after the vaccine (ex: sore arm, etc.) and only lasted for a few hours but no more than 24 hours for 1st dose, 2nd dose and Booster. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 18-Nov-2021: The additional information included suspect administration date. On 19-Nov-2021: Follow-up information included about patients details On 19-Nov-2021: Significant FU appended (Second reporter Information was updated)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 03.09.2021
- Beginn
- 09.09.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy
Blister
Blood test abnormal
Borrelia test negative
Herpes zoster
Hypersensitivity
Pruritus
Rash
Symptomtext
Rash initially started as a single itchy blister distal to injection site on anterior forearm. Rash multiplied into a shingles like rash- made a doctor's appointment and received antiviral medication. After 1 day of medication rash crossed the midline and was told it could be a poison ivy. Steroid cream prescribed and no relief given after several days. Rash continued to spread and evolved into a target lesion rash on both forearms, upper arms, chest, abdomen, thighs, calves, ankles, feet, toes, plantar surface, palms of hands, fingers, neck and face. Returned to doctor and was given a 12 day taper of prednisone. No relief of itching or spreading after 7 days. Rash started healing slowly and after finishing steroid, rash reappeared on right and left forearms, abdomen and thighs. Was referred to an allergist while on the steroid. Dr. did a blood test for lyme disease and shingles iGg. Lyme was negative, shingles iGg was positive, but not high enough to indicate recent outbreak. Rash started resolving after several days. One week after resolution, rash reappeared and Dr. performed a biopsy. Results of biopsy were hypersensitivity reaction. Rash is still reoccuring as of 11/18/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Blood test for Lyme and Shingles iGg- 10/06/2021 Lyme- negative Shingles iGg- positive Biopsy of rash- 10/18/2021 diagnosis- hypersensitivity reaction
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Malaise
Symptomtext
Malaise; Headache; This spontaneous case was reported by a pharmacist and describes the occurrence of MALAISE (Malaise) and HEADACHE (Headache) in a 42-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Oct-2021 at 8:00 AM, the patient experienced MALAISE (Malaise) and HEADACHE (Headache). At the time of the report, MALAISE (Malaise) and HEADACHE (Headache) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered MALAISE (Malaise) and HEADACHE (Headache) to be possibly related. No concomitant medications were provided. No treatment medication were provided. This case was linked to MOD-2021-370221 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Vaccination complication
Symptomtext
Malaise; Headache; This spontaneous case was reported by a pharmacist and describes the occurrence of VACCINATION COMPLICATION (Malaise) and HEADACHE (Headache) in a 24-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 3V (FLUARIX) injection for an unknown indication. No Medical History information was reported. On 29-Oct-2021, the patient started INFLUENZA VACCINE INACT SPLIT 3V (FLUARIX) (Intramuscular) 1 dosage form. On 29-Oct-2021 at 1:00 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Oct-2021 at 8:00 AM, the patient experienced VACCINATION COMPLICATION (Malaise) and HEADACHE (Headache). At the time of the report, VACCINATION COMPLICATION (Malaise) and HEADACHE (Headache) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered VACCINATION COMPLICATION (Malaise) and HEADACHE (Headache) to be possibly related. No treatment drugs were reported. No concomitants were reported. This case was linked to MOD-2021-370379 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Malaise
Symptomtext
Malaise; Headache; This spontaneous case was reported by a pharmacist and describes the occurrence of MALAISE (Malaise) and HEADACHE (Headache) in a 42-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Previously administered products included for an unreported indication: FLUARIX (Route: IM Body Site: Right Deltoid Lot No:379TF). On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 30-Oct-2021, the patient experienced MALAISE (Malaise) and HEADACHE (Headache). At the time of the report, MALAISE (Malaise) and HEADACHE (Headache) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment and concomitant medications were provided. Action taken with mRNA-1273 in response to the event was not applicable. This case concerns a 42-year-old, female patient, with no relevant medical history, who experienced the non-serious unexpected event of malaise and non-serious expected event of headache. The events occurred 1 day after booster dose of mRNA 1273 vaccine. The rechallenge for third dose is not applicable as no additional dose is expected. The events were considered related to the product per the reporter's assessment. The benefit-risk relationship of mRNA 1273 vaccine is not affected by this report This case was linked to MOD-2021-370222 (Patient Link).; Sender's Comments: This case concerns a 42-year-old, female patient, with no relevant medical history, who experienced the non-serious unexpected event of malaise and non-serious expected event of headache. The events occurred 1 day after booster dose of mRNA 1273 vaccine. The rechallenge for third dose is not applicable as no additional dose is expected. The events were considered related to the product per the reporter's assessment. The benefit-risk relationship of mRNA 1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Malaise
Symptomtext
Malaise; Headache; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 09-Nov-2021 and was forwarded to Moderna on 09-Nov-2021. This spontaneous case was reported by a pharmacist and describes the occurrence of MALAISE (Malaise) and HEADACHE (Headache) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Oct-2021 at 8:00 AM, the patient experienced MALAISE (Malaise) and HEADACHE (Headache). At the time of the report, MALAISE (Malaise) and HEADACHE (Headache) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered MALAISE (Malaise) and HEADACHE (Headache) to be possibly related. No concomitant products were reported. No treatment drugs were reported. This case was linked to MOD-2021-370370 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Malaise
Symptomtext
Malaise; Headache; This spontaneous case was reported by a pharmacist and describes the occurrence of MALAISE (Malaise) and HEADACHE (Headache) in a 40-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: FLUARIX (GSK, Lot number 379TF, Intramuscular route. Right Deltoid and First dose.). On 29-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Oct-2021, the patient experienced MALAISE (Malaise) and HEADACHE (Headache). At the time of the report, MALAISE (Malaise) and HEADACHE (Headache) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered MALAISE (Malaise) and HEADACHE (Headache) to be possibly related. No concomitant and treatment medications were provided This case was linked to MOD-2021-370174 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Malaise
Symptomtext
Malaise; Headache; This spontaneous case was reported by a pharmacist and describes the occurrence of MALAISE (Malaise) and HEADACHE (Headache) in a 56-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 3V (FLUARIX) for Vaccination. No Medical History information was reported. On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form and first dose of INFLUENZA VACCINE INACT SPLIT 3V (FLUARIX) (Intramuscular) 1 dosage form. On 30-Oct-2021, the patient experienced MALAISE (Malaise) and HEADACHE (Headache). At the time of the report, MALAISE (Malaise) and HEADACHE (Headache) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered MALAISE (Malaise) and HEADACHE (Headache) to be possibly related. No treatment medications were provided. This case was linked to MOD-2021-370320 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Malaise
Symptomtext
Malaise; Headache; This spontaneous case was reported by a pharmacist and describes the occurrence of MALAISE (Malaise) and HEADACHE (Headache) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 3V (FLUARIX) for an unknown indication. No Medical History information was reported. On 29-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient received first dose of INFLUENZA VACCINE INACT SPLIT 3V (FLUARIX) (Intramuscular) 1 dosage form. On 30-Oct-2021, the patient experienced MALAISE (Malaise) and HEADACHE (Headache). At the time of the report, MALAISE (Malaise) and HEADACHE (Headache) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. No treatment information was reported. This case concerns a 62-year-old, female patient with relevant medical history of concomitant Influenza vaccination, who experienced the unexpected non-serious event of Malasie and the expected non-serious event of Headache. The events occurred approximately 1 day after the second dose of mRNA-1273 Vaccine. The rechallenge was unknown since no information about the events of the first dose was disclosed. The patient's medical history of concomitant Influenza vaccination remain as a confounder for the occurrence of the events. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. This case was linked to MOD-2021-370266 (Patient Link).; Sender's Comments: This case concerns a 62-year-old, female patient with relevant medical history of concomitant Influenza vaccination, who experienced the unexpected non-serious event of Malasie and the expected non-serious event of Headache. The events occurred approximately 1 day after the second dose of mRNA-1273 Vaccine. The rechallenge was unknown since no information about the events of the first dose was disclosed. The patient's medical history of concomitant Influenza vaccination remain as a confounder for the occurrence of the events. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Malaise
Symptomtext
Malaise; Headache; This spontaneous case was reported by a pharmacist and describes the occurrence of MALAISE (Malaise) and HEADACHE (Headache) in a 60-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 3V (FLUARIX) for Vaccination. No Medical History information was reported. On 29-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient received dose of INFLUENZA VACCINE INACT SPLIT 3V (FLUARIX) (Intramuscular) 1 dosage form. On 30-Oct-2021, the patient experienced MALAISE (Malaise) and HEADACHE (Headache). At the time of the report, MALAISE (Malaise) and HEADACHE (Headache) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered MALAISE (Malaise) and HEADACHE (Headache) to be possibly related. No concomitant medications information was reported. No treatment medications were provided. This case was linked to MOD-2021-370191 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Malaise
Symptomtext
Malaise; Headache; This spontaneous case was reported by a pharmacist and describes the occurrence of MALAISE (Malaise) and HEADACHE (Headache) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Co-suspect product included non-company product INFLUENZA VACCINE INACT SAG 4V (FLUAD QUAD) for Vaccination. No Medical History information was reported. On 29-Oct-2021 at 1:00 AM, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form and INFLUENZA VACCINE INACT SAG 4V (FLUAD QUAD) (Intramuscular) 1 dosage form. On 30-Oct-2021 at 8:00 AM, the patient experienced MALAISE (Malaise) and HEADACHE (Headache). At the time of the report, MALAISE (Malaise) and HEADACHE (Headache) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered MALAISE (Malaise) and HEADACHE (Headache) to be possibly related. No treatment and concomitant medications were provided. This case was linked to MOD-2021-370445 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Pyrexia
Vaccination site erythema
Vaccination site mass
Vaccination site pruritus
Vaccination site reaction
Vaccination site warmth
Symptomtext
Left arm was itchy; Top of arm 4 inch down was red, hot and had a hard lump; covid arm; Top of arm 4 inch down was red, hot and had a hard lump; Top of left arm 4 inch down was red, hot and had a hard lump; Slight fever of 98.4-98.6; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (Left arm was itchy), AXILLARY MASS (Top of arm 4 inch down was red, hot and had a hard lump), VACCINATION SITE REACTION (covid arm), FEELING HOT (Top of arm 4 inch down was red, hot and had a hard lump) and ERYTHEMA (Top of left arm 4 inch down was red, hot and had a hard lump) in an 84-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included AFib in 2019. Previously administered products included for Product used for unknown indication: Flu shot in October 2021. Past adverse reactions to the above products included No adverse event with Flu shot. Concurrent medical conditions included Cancer. Concomitant products included APIXABAN (ELIQUIS), DILTIAZEM and LEVOTHYROXINE for an unknown indication. On 28-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 ml. On 29-Oct-2021, the patient experienced PRURITUS (Left arm was itchy), AXILLARY MASS (Top of arm 4 inch down was red, hot and had a hard lump), VACCINATION SITE REACTION (covid arm), FEELING HOT (Top of arm 4 inch down was red, hot and had a hard lump), ERYTHEMA (Top of left arm 4 inch down was red, hot and had a hard lump) and PYREXIA (Slight fever of 98.4-98.6). On 31-Oct-2021, PYREXIA (Slight fever of 98.4-98.6) had resolved. On 01-Nov-2021, ERYTHEMA (Top of left arm 4 inch down was red, hot and had a hard lump) had resolved. At the time of the report, PRURITUS (Left arm was itchy), AXILLARY MASS (Top of arm 4 inch down was red, hot and had a hard lump), VACCINATION SITE REACTION (covid arm) and FEELING HOT (Top of arm 4 inch down was red, hot and had a hard lump) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 29-Oct-2021, Body temperature: 98.4-98.6 (Low) slight fever of 98.4-98.6. No treatment medication was reported. This case was linked to MOD-2021-370414 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211029; Test Name: Body temperature; Result Unstructured Data: slight fever of 98.4-98.6
- Aktuelle Erkrankungen
- Cancer
- Vorgeschichte
- Medical History/Concurrent Conditions: AFib
- Andere Medikamente
- ELIQUIS; DILTIAZEM; LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- 29.09.2021
- Beginn
- 07.10.2021
- Tage bis Beginn
- 8,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Myalgia
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 COVID-19 (1st dose) and MYALGIA in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 049E21A and 039D21A) for COVID-19 vaccination. Medical history was not reported. Concomitant products included GABAPENTIN and MELATONIN for an unknown indication. On 29-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Oct-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 07-Oct-2021, the patient experienced COVID-19 (1st dose). On an unknown date, the patient experienced MYALGIA. The patient was treated with TYLENOL for Adverse event, at an unspecified dose and frequency. At the time of the report, COVID-19 (1st dose) and MYALGIA outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) and mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. This case concerns a 27-year-old, female patient with no relevant medical history reported, who experienced the unexpected non-serious AESI event of COVID-19. The event occurred approximately 9 days after the first dose of Moderna COVID-19 vaccine. The benefit-risk relationship of Moderna COVID-19 vaccine is not affected by this report. This case was linked to MOD-2021-370418 (Patient Link). This case concerns a 27-year-old, female patient with no relevant medical history reported, who experienced the unexpected non-serious AESI event of COVID-19. The event occurred approximately 9 days after the first dose of Moderna COVID-19 vaccine. The benefit-risk relationship of Moderna COVID-19 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Medical history was not reported.
- Andere Medikamente
- GABAPENTIN; MELATONIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 07.11.2021
- Impfdatum
- 28.09.2021
- Beginn
- 28.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Arthralgia
Asthenia
Hypoaesthesia
Joint swelling
Laboratory test
Magnetic resonance imaging head
Magnetic resonance imaging neck
Nausea
Photophobia
Symptomtext
With in 15 mins the right side of my face went numb, street lights and car lights hurt my eyes. Within an hour my right arm was numb, I felt sick to my stomach and I was weak. Went to bed my right arm and face stayed completely numb for 2 days. When I did start getting feeling back my arm was weak. And as of 11/07/2021 my right side of my body is still week, my face and arm still goes numb. I still feel nauseated and I have had pain and swelling in my joints, extremely bad on the right half of my body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Seen my doctor on 11/05/2021. He has ordered an MRI of the brain and cervical. That will be preformed on 11/19/2021. He also ordered lab work that was preformed 11/05/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- No spleen, only half a pancreas. Melanoma, hypothyroidism, digestive issues.
- Andere Medikamente
- Creon Dr 36,000 unit, potassium cl er 20 meq, Magnesium oxide 400 mg, Omeprazole Dr 40 mg, Levothyroxine 75mcg, furosemide 40 mg Lactulose 30 mls
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 07.10.2021
- Beginn
- 07.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Influenza like illness
Lymphadenopathy
Symptomtext
The first thing I started to feel was pain under my arm. Swollen lymph nodes under left arm. Flu like symptoms that night and gone the next morning. Swollen and pain under my arm lasted for 10 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma
- Andere Medikamente
- Yes
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Fatigue
Nasal congestion
Pain
Product storage error
Symptomtext
Booster dose. Vaccine administered on 11/01/21. Vial expired 10/11/21. Vial was kept in freezer until 10/30/2021 and removed to fridge on 10/30/2021 for administration on 11/01/2021. pt reports chills, body aches, fatigue, stuffy nose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 31.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 02.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Cold sweat
Decreased appetite
Dizziness
Fatigue
Feeling cold
Heart rate increased
Malaise
Pyrexia
Symptomtext
Little or no symptoms for the first 24 hours, then they set in as follows: rapid heart rate >100 bpm even while resting, crushing fever, extreme fever switching between unable to get warm or in succession cold sweats, loss of appetite, fatigue, dizzy with loss of equilibrium, malaise, pretty much didn't do anything for several days (3 or more)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- did no test, saw no doctor, stayed home
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Asthma since birth
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 30.10.2021
- Impfdatum
- 27.08.2021
- Beginn
- 27.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Bone pain
Chills
Dizziness
Dyspepsia
Eructation
Fatigue
Feeling cold
Flatulence
Hot flush
Hyperhidrosis
Memory impairment
Narcolepsy
Night sweats
Nocturia
Peripheral swelling
Retching
Trigger finger
Symptomtext
She states started evening on the day of the vaccine with the first week severe and still experiencing symptoms in October. She says has been having extreme fatigue, hearburn with dry heaves and vomiting, leg and hand swelling (improving now), night sweats (4 am soaking sheets) and nocturesis, bone aches including a trigger finger acting up (had been better until got vaccine), excess gas/burping, hot/cold flashes, sweats and chills daily, feeling woozy and unsteady, narcolepsy episodes often the first week but still occurring occasionally, possible memory issues. She has been in touch with her doctor on this and reports gradual improvement. She will be consulting a specialist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bone pain
- Hospital-Tage
- -
- Labordaten
- none known
- Aktuelle Erkrankungen
- tooth abscess current
- Vorgeschichte
- fibromyalgia
- Andere Medikamente
- Metoprolol Succ ER 200 mg daily Amlodipine 10 mg daily Desvenlafaxine Succ ER 100 mg daily Buspirone 15 mg tab three times daily Gabapentin 100 mg three times daily Dextroamp-amphet 20 mg tab up to 2 BID HydrocodAcet 10-325 mg 1 to 2 every
- Allergien
- NKDA
- Vorherige Impfungen
- previous VAERS 12/12/2020 : Flucelvax, Adacel, Pneumovax 23, Shingrix
- Staat
- WA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 08.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Formication
Rash
Skin burning sensation
Urticaria
Symptomtext
Hives. Rash. Burning sensation on skin. Feels like creatures crawling under my skin. At least ten times worse feeling than when I actually had Covid 19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Doctor refuses to see me because I told them I had adverse reaction to the vaccine
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Inhaler
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 23.10.2021
- Impfdatum
- 15.09.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site bruising
Vaccination site pain
Symptomtext
She has a discoloration at the injection site of the first dose and can still feel the first shot, is this normal? It is brown in color, like a bruise; can still feel the first shot/ still has pain at the injection site of the first dose.; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE BRUISING (She has a discoloration at the injection site of the first dose and can still feel the first shot, is this normal? It is brown in color, like a bruise) and VACCINATION SITE PAIN (can still feel the first shot/ still has pain at the injection site of the first dose.) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In September 2021, the patient experienced VACCINATION SITE BRUISING (She has a discoloration at the injection site of the first dose and can still feel the first shot, is this normal? It is brown in color, like a bruise) and VACCINATION SITE PAIN (can still feel the first shot/ still has pain at the injection site of the first dose.). At the time of the report, VACCINATION SITE BRUISING (She has a discoloration at the injection site of the first dose and can still feel the first shot, is this normal? It is brown in color, like a bruise) and VACCINATION SITE PAIN (can still feel the first shot/ still has pain at the injection site of the first dose.) had not resolved. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. No Concomitant medications were reported. No treatment information was provided. This case was linked to MOD-2021-352988 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 20.10.2021
- Impfdatum
- 22.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Hypersensitivity
Rhinorrhoea
Sneezing
Symptomtext
running nose; sneezing; allergy reaction; terrible diarrhea; This spontaneous case was reported by a consumer and describes the occurrence of DIARRHOEA (terrible diarrhea), RHINORRHOEA (running nose), SNEEZING (sneezing) and HYPERSENSITIVITY (allergy reaction) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Sep-2021, the patient experienced DIARRHOEA (terrible diarrhea). On an unknown date, the patient experienced RHINORRHOEA (running nose), SNEEZING (sneezing) and HYPERSENSITIVITY (allergy reaction). At the time of the report, DIARRHOEA (terrible diarrhea) had not resolved and RHINORRHOEA (running nose), SNEEZING (sneezing) and HYPERSENSITIVITY (allergy reaction) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medication details was reported. No treatment medication details was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 18.10.2021
- Impfdatum
- 15.10.2021
- Beginn
- 17.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Injection site pain
Injection site reaction
Rash macular
Symptomtext
After the 2nd shot on 10/15, I had a bad headache on 10/16 and 10/17. On 10/17 my arm had red blotches going down to my elbow underneath the injection site and hurt like bad bruises.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- 50 mg levothyroxine, prenatal vitamin, fish oil vitamin, and sunflower lecithin for breastfeeding
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Therapeutic response unexpected
Vaccination site pain
Symptomtext
second dose and is still feeling wonderful/feels wonderfull/"I don't ever feel this good"/I feel 20 years younger/; soreness at the injection site after second dose/soreness: worse on the second day, can still feel a little tiny bit when moving the arm, almost gone; pain at the injection site after second dose; This spontaneous case was reported by a consumer and describes the occurrence of THERAPEUTIC RESPONSE UNEXPECTED (second dose and is still feeling wonderful/feels wonderfull/"I don't ever feel this good"/I feel 20 years younger/), MYALGIA (soreness at the injection site after second dose/soreness: worse on the second day, can still feel a little tiny bit when moving the arm, almost gone) and VACCINATION SITE PAIN (pain at the injection site after second dose) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Medical history was not provided by the reporter. Concurrent medical conditions included Cramps, Coronary artery disease and Pain (before the vaccine). Concomitant products included AMLODIPINE BESILATE (NORVAC) for Coronary artery disease, OMEPRAZOLE for Stomach cramps, CLOPIDOGREL BISULFATE (PLAVIX) and ROSUVASTATIN CALCIUM (CRESTOR) for an unknown indication. On 05-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Oct-2021, the patient experienced THERAPEUTIC RESPONSE UNEXPECTED (second dose and is still feeling wonderful/feels wonderfull/"I don't ever feel this good"/I feel 20 years younger/), MYALGIA (soreness at the injection site after second dose/soreness: worse on the second day, can still feel a little tiny bit when moving the arm, almost gone) and VACCINATION SITE PAIN (pain at the injection site after second dose). At the time of the report, THERAPEUTIC RESPONSE UNEXPECTED (second dose and is still feeling wonderful/feels wonderfull/"I don't ever feel this good"/I feel 20 years younger/) outcome was unknown and MYALGIA (soreness at the injection site after second dose/soreness: worse on the second day, can still feel a little tiny bit when moving the arm, almost gone) and VACCINATION SITE PAIN (pain at the injection site after second dose) was resolving. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient was taking concomitant medications for cramps and coronary artery problems. No treatment medication were reported This case was linked to MOD-2021-346776 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Coronary artery disease; Cramps; Pain (before the vaccine.)
- Vorgeschichte
- Comments: Medical history was not provided by the reporter.
- Andere Medikamente
- NORVAC; PLAVIX; CRESTOR; OMEPRAZOLE.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 07.09.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Therapeutic response unexpected
Vaccination site pain
Symptomtext
second dose and is still feeling wonderful/feels wonderful/after the first dose noticed that the joints didn't hurt for a couple days/after first dose noticed that muscles didn't hurt for a couple days/"I don't ever feel good/I feel 20 years young; soreness at the site of injection after first dose; pain at the site of injection after first dose; This spontaneous case was reported by a consumer and describes the occurrence of THERAPEUTIC RESPONSE UNEXPECTED (second dose and is still feeling wonderful/feels wonderful/after the first dose noticed that the joints didn't hurt for a couple days/after first dose noticed that muscles didn't hurt for a couple days/"I don't ever feel good/I feel 20 years younger), MYALGIA (soreness at the site of injection after first dose) and VACCINATION SITE PAIN (pain at the site of injection after first dose) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Concurrent medical conditions included Cramps, Coronary artery disease and Pain (before the vaccine). Concomitant products included AMLODIPINE BESILATE (NORVASC) for Coronary artery disease, OMEPRAZOLE for Stomach cramps, CLOPIDOGREL BISULFATE (PLAVIX) and ROSUVASTATIN CALCIUM (CRESTOR) for an unknown indication. On 07-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In September 2021, the patient experienced THERAPEUTIC RESPONSE UNEXPECTED (second dose and is still feeling wonderful/feels wonderful/after the first dose noticed that the joints didn't hurt for a couple days/after first dose noticed that muscles didn't hurt for a couple days/"I don't ever feel good/I feel 20 years younger), MYALGIA (soreness at the site of injection after first dose) and VACCINATION SITE PAIN (pain at the site of injection after first dose). At the time of the report, THERAPEUTIC RESPONSE UNEXPECTED (second dose and is still feeling wonderful/feels wonderful/after the first dose noticed that the joints didn't hurt for a couple days/after first dose noticed that muscles didn't hurt for a couple days/"I don't ever feel good/I feel 20 years younger) outcome was unknown and MYALGIA (soreness at the site of injection after first dose) and VACCINATION SITE PAIN (pain at the site of injection after first dose) was resolving. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient was taking concomitant medications for cramps and coronary artery problems. No treatment medications were reported. This case was linked to MOD-2021-346886 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Coronary artery disease; Cramps; Pain (before the vaccine).
- Vorgeschichte
- -
- Andere Medikamente
- Norvasc; Plavix; Crestor; Omeprazole
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 28.08.2021
- Beginn
- 28.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Product dose omission issue
Symptomtext
I'm a little late for my 2nd shot.; I had minor soreness in my arm from the injection.; This spontaneous case was reported by a consumer and describes the occurrence of INJECTION SITE PAIN (I had minor soreness in my arm from the injection.) and PRODUCT DOSE OMISSION ISSUE (I'm a little late for my 2nd shot.) in a 37-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Aug-2021, the patient experienced INJECTION SITE PAIN (I had minor soreness in my arm from the injection.). On 08-Oct-2021, the patient experienced PRODUCT DOSE OMISSION ISSUE (I'm a little late for my 2nd shot.). At the time of the report, INJECTION SITE PAIN (I had minor soreness in my arm from the injection.) and PRODUCT DOSE OMISSION ISSUE (I'm a little late for my 2nd shot.) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided by reporter. No Treatment medications were provided by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 15.10.2021
- Impfdatum
- 06.08.2021
- Beginn
- 07.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Skin lesion
Symptomtext
Patient broken out in open sore lesions on his face and head that turned into scabs for 2-3 days following administration of the vaccine. He also reported having itchy lower extremities for 2-3 days following administration of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 13.10.2021
- Impfdatum
- 28.09.2021
- Beginn
- 03.10.2021
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chills
Hyperhidrosis
Hypoaesthesia
Pain
Peripheral swelling
Pyrexia
Swelling face
Symptomtext
Per patient: had a normal reaction during the first 4 days including sweats, chills, body aches, and fever. On day 5, patient reported have facial numbness and swelling effecting half the face. Went to the hospital and noted that numbness spread to the entire face. Was sent home after 12 hours. On day 6, he reported swelling of extremities (hands/feet) and returned to the hospital. He said he was given epinephrine at the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unkown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 07.10.2021
- Beginn
- 08.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash pruritic
Symptomtext
Wide spread itchy rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- B12, Biotin, Wellbutrin and Melatonin
- Allergien
- Compuzine and Reglan
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 12.10.2021
- Impfdatum
- 14.09.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Injection site pain
Symptomtext
The next day severe pain at shot location on arm. Constant Severe joint pain in shoulders, hips and knees. This pain was continuous and no amount of pain reliever medicine would work. My pain management doctor increased my dose of Tramadol to 2 every 4 to 6 hours with Tylenol or aspirin in-between and it did not help. The pain finally stopped when I woke up on the 8th of October, 23 days later. I took the 2nd dose today 10/12/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- No lab or medical tests done
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- Impfdatum
- 18.08.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 21,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Burning sensation
COVID-19
Erythema
Headache
Herpes zoster
Swelling
Symptomtext
I initially woke up with intense burning/pain on my forehead. Over the next few days, the site of the pain became red, swollen, and blistered. I went to the urgent care at Hospital on September 11. They thought I had a skin infection (but could possibly be Shingles) and prescribed antibiotics. The antibiotics were not helping and the blisters were spreading (across my face, around my eye, under my hair--all on the right side) so I went to a different urgent care location on September 13. They told me that it looked like I had Shingles and prescribed Valacyclovir 1000 mg twice/day. That started helping, but the Shingles persisted for quite a while. I also had to visit an eye doctor because the Shingles were around my eye. He prescribed additional medication for me, which I am still taking now (Acyclovir). Two out of the three doctors I saw said that this could have definitely been triggered by the vaccine. Consequently I was not able to get the second dose, and I'm not sure that I want to. While my immune system was down because of the Shingles, I ended up contracting COVID. I am currently fighting that as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- September 11: Urgent Care visit (given antibiotics) September 13: Urgent Care visit (given Valacyclovir) September 13: Urgent Care visit (later filled a prescription for Acyclovir when the Shingles persisted) October 3: Positive COVID test October 4: Antibody Infusion
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Escitalopram
- Allergien
- Peanuts
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- 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
Breast swelling
Injection site pain
Injection site swelling
Neck pain
Oedema peripheral
Peripheral swelling
Pyrexia
Swelling
Symptomtext
Starting on 10/6/2021 I had swelling under my left arm and a 102 fever. I took Tylenol for the fever. On 10/7/2021 and continuing, I still have the swelling under my arm which has gone into my left breast, my left breast is visably swollen, there is more swelling on my left sholder into my neck and down my back. My left arm is swollen and the sleeves of my shirts on the left side are noticibly tighter than on the right, my bicep is swollen and is painful. I feel pain in my neck, most likely from the swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- I'm going to the doctor today at noon.
- Aktuelle Erkrankungen
- NONE!!!!!!!
- Vorgeschichte
- Heart disease
- Andere Medikamente
- Metformin, Isosorbide Dinitrate, Simvastatin, Etodolac, Vitamin D, Zinc
- Allergien
- Ceclor, Silver Sulfadiazine
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 08.10.2021
- Impfdatum
- 11.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 21,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Computerised tomogram
Diarrhoea haemorrhagic
Fatigue
Feeling abnormal
Pain in extremity
Symptomtext
After the first shot I had a lot of pain and sore in my arm and fatigue. It lasted about 3 weeks. After the second shot, it seemed like the pain was more intense. But the fatigue was worse. My diarrhea turned bloody. I have been in this brain fog. I cannot even find words that I want to say. I went to the hospital on 09/30/2021. They did a CT scan of my torso with and without contrast. They did blood work. They gave me IV because I was very dehydrated. I saw a GI specialist yesterday. He is going to scope me. I am supposed to get a stomach X-ray and blood work today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea haemorrhagic
- Hospital-Tage
- -
- Labordaten
- CT scan of my torso with and without contrast- I do not have the results; Blood work- I do not have the results
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic diarrhea since 2019; rheumatoid arthritis
- Andere Medikamente
- Vitamin D3; vitamin B12; estradiol; hydrochlorothiazide; rosuvastatin calcium; diclofenac; losartan potassium
- Allergien
- Latex; adhesive; gabapentin; LYRICA; WELLBUTRIN; lithium
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 19.08.2021
- Beginn
- 22.08.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Hypoaesthesia
Myalgia
SARS-CoV-2 test
Symptomtext
contracted COVID-19 a mild case; numbness on her face for several days; muscle pain in legs,muscle pain in jaw; chills; This spontaneous case was reported by a patient and describes the occurrence of HYPOAESTHESIA (numbness on her face for several days), COVID-19 (contracted COVID-19 a mild case), CHILLS (chills) and MYALGIA (muscle pain in legs,muscle pain in jaw) in a 60-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Aug-2021, the patient experienced CHILLS (chills). On 24-Aug-2021, the patient experienced HYPOAESTHESIA (numbness on her face for several days) and MYALGIA (muscle pain in legs,muscle pain in jaw). On 26-Aug-2021, the patient experienced COVID-19 (contracted COVID-19 a mild case). At the time of the report, HYPOAESTHESIA (numbness on her face for several days), COVID-19 (contracted COVID-19 a mild case), CHILLS (chills) and MYALGIA (muscle pain in legs,muscle pain in jaw) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 26-Aug-2021, SARS-CoV-2 test: positive Positive. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Her concerned is about getting the second dose because she had COVID. Concomitant medication use was unknown Treatment information was unknown Reporter did not allow further contact; Sender's Comments: This spontaneous case concerns a 60-year-old female patient with no relevant medical history reported, who experienced non serious unexpected events of hypoesthesia, COVID-19 and expected events of myalgia and chills. The events occurred 3-7 days after the first dose of Spikevax. Rechallenge was unknown since information about second dose and reoccurrence of the event was not provided. The benefit-risk relationship of drug is not affected by this report
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210826; Test Name: Covid test; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 05.10.2021
- Impfdatum
- 22.09.2021
- Beginn
- 26.09.2021
- Tage bis Beginn
- 4,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Urticaria
Symptomtext
Hive breakout on face that lasts for 10-20 minutes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- 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: ja
Chills
Decreased appetite
Dysgeusia
Fatigue
Feeling abnormal
Headache
Pain
Symptomtext
Chills, swimmy head, extreme tiredness, soreness throughout entire body, headache, weird after taste in mouth, no appetite
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 23.08.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vomiting
Symptomtext
throwing up for the past day; This spontaneous case was reported by a consumer and describes the occurrence of VOMITING (throwing up for the past day) in a 25-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 039D21A and 049E21A) for COVID-19 vaccination. The patient's past medical history included Psoriasis. On 23-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 20-Sep-2021, the patient experienced VOMITING (throwing up for the past day). At the time of the report, VOMITING (throwing up for the past day) outcome was unknown. No concomitant medications reported. No treatment medications reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Psoriasis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 29.09.2021
- Impfdatum
- 27.09.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Fatigue
Headache
Injection site pain
Pain
Symptomtext
Very sore left arm. Headache. Body aches. Tired. Lasted 1-1/2 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- 2/4/21 Covid, Moderna - severe rash. 3/9/21 Covid, Moderna - Flu-like symptoms + fever
- Staat
- WA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 28.09.2021
- Impfdatum
- 15.09.2021
- Beginn
- 16.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Fatigue
Headache
Heart rate increased
Hypersomnia
Injection site pain
Loss of personal independence in daily activities
Lymphadenopathy
Medication error
Sleep disorder
Swelling
Symptomtext
Alongside headache and fatigue, I experienced notably increased heart rate. I have chronic tachycardia, likely [non-covid-related] POTS (and several medications that worsen this as a side effect), but I take Metoprolol to treat this. As a result, I typically have an HR of 80-95 when sitting at rest. On the 16th, it was 120-140+ when sitting/laying at rest. After my first appointment of the day, I had to drop the rest of my plans to rest, and I slept about 16 hours. This also happened after the second dose, but I was unsure if it was related to the vaccine, as I had made several errors with my daily medications that week and had gotten little sleep. This was not the case after third dose, yet the symptoms were worse. After 16 hours of sleep, the symptoms largely subsided, and if boosters were to be offered annually going forward, I would continue to take them despite these symptoms, but the effect on my HR was arguably substantive, so I figured I should report. *I also had soreness at the injection site, which was mild and expected. I also had swelling of my lymph nodes on the left side only, at the base of my neck. I've never had this reaction to a vaccine before, including previous doses of this vaccine (all Moderna), and I've never had swelling this extreme from an active infection either.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Ehlers Danlos Syndrome (Q79.62); Chronic Sinus Tachycardia (Possible Postural Orthostatic; Tachycardia Syndrome - I49.8); not caused by COVID-19; Depression, Anxiety Disorders; Suspected Endometriosis
- Andere Medikamente
- 1x/day: Metoprolol Succinate 25 mg; Bupropion HCl XL 300 mg; Orilissa (Elagolix) 150 mg; Valacyclovir HCl 500 mg; Atomoxetine 80 mg; Vitamins: Vitamin D 2.5-5k IU, Vitamin B12 1000 mcg, Vitamin C 282 mg, Calcium 500 mg, Women's Multivitami
- Allergien
- Nickel: swelling; Dronabinol: swelling/hives/nausea; Pumpkin (Flesh): hives; Ligustrum vulgare (Common Privet): congestion/watery eyes; Kochia scoparia (Invasive Weed): swelling/hives/nausea
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 28.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 25.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site bruising
Pain in extremity
Symptomtext
Reports sore arm that lasted more than a few days that required multiple doses of over the counter acetaminophen. Patient also iced. When pharmacy examined arm, there was a dark, yet fading, bruise ~5" down from injection area. When arriving to pharmacy 9/26/21 the bruise was in healing process and patient wasn't in pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 28.09.2021
- Impfdatum
- 20.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Symptomtext
Tiredness; This spontaneous case was reported by a consumer and describes the occurrence of FATIGUE (Tiredness) in a 58-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No medical history was reported. On 20-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced FATIGUE (Tiredness). The patient was treated with IBUPROFEN for Adverse event, at an unspecified dose and frequency and PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency. At the time of the report, FATIGUE (Tiredness) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant product use was provided by the reporter. This case was linked to MOD-2021-325991 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was reported
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 27.09.2021
- Impfdatum
- 14.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
Headache every single day since I received my first dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Barrett's Esophagus
- Andere Medikamente
- Nexium Vitamins
- Allergien
- Prilosec
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 25.09.2021
- Beginn
- 26.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Broke out in hives one day following 2nd injection of Moderna. Hives started on neck and chest and continue to move upwards towards my right and left side of neck, and down the right side of my arm (side the injection was given).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec
- Allergien
- Penicillin, Microdantin, Macrobid
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 25.09.2021
- Impfdatum
- 12.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Nausea
Visual impairment
Vomiting
Symptomtext
vision issues(seeing lightning bolts, dark spots), nausea, vomiting, muscle pain Ongoing- not resolved Moderna COVID-19 Vaccine EUA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- neuropothy
- Vorgeschichte
- asthma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 25.09.2021
- Impfdatum
- 16.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Chest discomfort
Chills
Cough
Dysphonia
Heart rate
Pyrexia
Rhinorrhoea
SARS-CoV-2 test
Symptomtext
Tight in the chest; Cramping right at the top around my stomach; Runny nose; Dry cough; Hoarseness in her voice; Chills; Fever; This spontaneous case was reported by a consumer and describes the occurrence of CHEST DISCOMFORT (Tight in the chest), ABDOMINAL PAIN UPPER (Cramping right at the top around my stomach), RHINORRHOEA (Runny nose), COUGH (Dry cough) and DYSPHONIA (Hoarseness in her voice) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Atypical angina (Atypical angina with coronary vasospasm 20 years ago), Coronary vasospasm, Norovirus infection in June 2021, Thrombus and Intestinal ischemia. Concurrent medical conditions included Tachycardia. Concomitant products included METOPROLOL for Tachycardia. On 16-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In 2021, the patient experienced CHEST DISCOMFORT (Tight in the chest), ABDOMINAL PAIN UPPER (Cramping right at the top around my stomach), RHINORRHOEA (Runny nose), COUGH (Dry cough), DYSPHONIA (Hoarseness in her voice), CHILLS (Chills) and PYREXIA (Fever). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) ongoing since an unknown date for Chills, at a dose of 1 dosage form. In 2021, RHINORRHOEA (Runny nose), COUGH (Dry cough), DYSPHONIA (Hoarseness in her voice), CHILLS (Chills) and PYREXIA (Fever) had resolved. At the time of the report, CHEST DISCOMFORT (Tight in the chest) and ABDOMINAL PAIN UPPER (Cramping right at the top around my stomach) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, SARS-CoV-2 test: negative (Negative) negative. On an unknown date, Heart rate: high (High) heart rate sometimes goes up to 165, but is currently around 75. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. This case was linked to MOD-2021-321079 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Test Name: heart rate; Result Unstructured Data: heart rate sometimes goes up to 165, but is currently around 75; Test Date: 2021; Test Name: COVID-19 test; Test Result: Negative ; Result Unstructured Data: negative
- Aktuelle Erkrankungen
- Tachycardia
- Vorgeschichte
- Medical History/Concurrent Conditions: Atypical angina (Atypical angina with coronary vasospasm 20 years ago); Coronary vasospasm; Intestinal ischemia; Norovirus infection; Thrombus
- Andere Medikamente
- METOPROLOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 25.09.2021
- Impfdatum
- 21.08.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Dizziness
Dysstasia
Fall
Fatigue
Gait disturbance
Headache
Pollakiuria
Symptomtext
Could hardly stand; headache; fatigue; little dizzy; barley walk; was falling in the walls; frequently urinate; This spontaneous case was reported by a patient and describes the occurrence of DIZZINESS (little dizzy), GAIT DISTURBANCE (barley walk), FALL (was falling in the walls), POLLAKIURIA (frequently urinate) and DYSSTASIA (Could hardly stand) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Liver transplant (12 year ago.) in November 2008. Concurrent medical conditions included Drug allergy (ciprofloxacin). Concomitant products included SIROLIMUS (RAPAMUNE) for Immunosuppressant drug level NOS, VITAMINS;MINERALS;LYSINE and CALCIUM for an unknown indication. On 21-Aug-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Aug-2021, the patient experienced DIZZINESS (little dizzy), GAIT DISTURBANCE (barley walk), FALL (was falling in the walls) and POLLAKIURIA (frequently urinate). On 22-Aug-2021, the patient experienced HEADACHE (headache) and FATIGUE (fatigue). On an unknown date, the patient experienced DYSSTASIA (Could hardly stand). The patient was treated with PARACETAMOL (TYLENOL) for Headache and Fatigue, at an unspecified dose and frequency. On 22-Aug-2021, DIZZINESS (little dizzy), GAIT DISTURBANCE (barley walk), FALL (was falling in the walls) and HEADACHE (headache) had resolved. At the time of the report, POLLAKIURIA (frequently urinate) and DYSSTASIA (Could hardly stand) outcome was unknown and FATIGUE (fatigue) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood test: 34,37,23,1.43, 40, 31.3,13.3 (High) ALT-34,AGT-39, BUN-23,CREATINE-1.43, DIRECT BILLI..-40, MCH-31.3, MID-13.3 and 57.20,7.0 (Low) GRANULOCYTES-57.20, MPV-7.0. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Reporter states that patient had blood test after 3 days of vaccination and liver and kidney level was elevated. patient will be going for another blood test after couple of days to see it return to normal. No treatment medications were provided. Most recent FOLLOW-UP information incorporated above includes: On 16-Sep-2021: Significant follow up events and new reporter and event outcome and tests are added , and I narrative updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Test Name: blood test; Result Unstructured Data: ALT-34,AGT-39, BUN-23,CREATINE-1.43, DIRECT BILLI..-40, MCH-31.3, MID-13.3; Test Name: Blood test; Result Unstructured Data: GRANULOCYTES-57.20, MPV-7.0
- Aktuelle Erkrankungen
- Drug allergy (ciprofloxacin)
- Vorgeschichte
- Medical History/Concurrent Conditions: Liver transplant (12 year ago.)
- Andere Medikamente
- VITAMINS;MINERALS;LYSINE; CALCIUM; RAPAMUNE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 23.09.2021
- Impfdatum
- 20.09.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Diarrhoea
Dizziness
Fatigue
Malaise
Pyrexia
Vomiting
Symptomtext
That evening after getting both injections patient started feeling unwell. Patient was fatigued and dizzy the next day following immunizations. Mild fever for about 6 to 8 hours. Vomiting and diarrhea was also present. Patient went to emergency room on wednesday. Discharged with anti-nausea and anti-diarrhea medications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- asthma, mild copd
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 22.09.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Myalgia
Pain
Symptomtext
Several hours after vaccination, patient experienced severe whole-body pain and myalgia. Went to emergency room where they administered IV opioid and anti-inflammatories. Patient states felt fine a few hours later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ICD-10: M34.1, M19.90, M79.7, m729.1
- Andere Medikamente
- methotrexate, hydroxychloroquine, folic acid, gabapentin, venlafaxine, quetiapine, clonazepam, methylphenidate
- Allergien
- penicillin, sulfa
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 22.09.2021
- Impfdatum
- 17.09.2021
- Beginn
- 17.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site nodule
Injection site pruritus
Injection site swelling
International normalised ratio increased
Symptomtext
Pt is on Warfarin. States her arm got "a knot" in the injection site about a hour and 15 minutes after injection. States It started itching that night and she scratched it and then a bruise started. The next day, she states her INR was increased. The patient has a home testing kit for INR checks. Her arm was swollen and badly bruised down right past her elbow. States she called her PCP and they told her to hold her Warfarin until it came down. Saw her PCP on 9/21/21. States on 9/22/21 her INR is returning to normal and the bruising and swelling is going down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- Penicillin rash
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 22.09.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 31,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Illness
Oral mucosal blistering
Oral pain
Stomatitis
Toothache
Vomiting
Symptomtext
mouth hurts; sores in her mouth/ mouth sores; mouth blisters started to appear; teeth felt sore; got sick; very weak; vomiting; chills; This spontaneous case was reported by a consumer and describes the occurrence of ILLNESS (got sick), ASTHENIA (very weak), TOOTHACHE (teeth felt sore), ORAL MUCOSAL BLISTERING (mouth blisters started to appear) and ORAL PAIN (mouth hurts) in a 32-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 048F21A and 049E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 11-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 11-Sep-2021, the patient experienced ILLNESS (got sick), ASTHENIA (very weak), VOMITING (vomiting) and CHILLS (chills). On 12-Sep-2021, the patient experienced TOOTHACHE (teeth felt sore). On 13-Sep-2021, the patient experienced ORAL MUCOSAL BLISTERING (mouth blisters started to appear). On 14-Sep-2021, the patient experienced ORAL PAIN (mouth hurts) and STOMATITIS (sores in her mouth/ mouth sores). The patient was treated with PARACETAMOL (TYLENOL) ongoing since an unknown date for Sore mouth, at a dose of 1 dosage form. At the time of the report, ILLNESS (got sick), ASTHENIA (very weak), TOOTHACHE (teeth felt sore), ORAL MUCOSAL BLISTERING (mouth blisters started to appear), ORAL PAIN (mouth hurts), STOMATITIS (sores in her mouth/ mouth sores), VOMITING (vomiting) and CHILLS (chills) outcome was unknown. No concomitant medications was provided by the reporter. Patient stated she has never had mouth blisters like this in the past. She stated that she doesn't take any medications daily. She reported that she was not pregnant. Most recent FOLLOW-UP information incorporated above includes: On 14-Sep-2021: Non significant follow up On 14-Sep-2021: Follow up information added patient identities, vaccine information, Events and treatment drug were updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 14.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy to vaccine
Myalgia
Symptomtext
ALLERGY SYMPTOMS; She is sore; This spontaneous case was reported by a consumer and describes the occurrence of ALLERGY TO VACCINE (ALLERGY SYMPTOMS) and MYALGIA (She is sore) in a 20-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No medical history was provided by reporter. No concomitant medication reported. No treatment medication reported. On 14-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1. On an unknown date, the patient experienced ALLERGY TO VACCINE (ALLERGY SYMPTOMS) and MYALGIA (She is sore). At the time of the report, ALLERGY TO VACCINE (ALLERGY SYMPTOMS) and MYALGIA (She is sore) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No medical history was provided by reporter. No concomitant medication reported. No treatment medication reported Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by reporter. No concomitant medication reported. No treatment medication reported.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 20.09.2021
- Impfdatum
- 28.08.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Skin swelling
Steroid therapy
Urticaria
Symptomtext
about 4 days after receiving the vaccine I began to observe hives in a variety of locations. No hives ever appeared near the injection site itself. Locations most affected are neck, head/face, hands, groin, and lower legs/feet. The hives seem to be reactive to touching and heat. If I draw a line lightly on my skin with my finger, 30 secons later the entire line will be raised and colored deep red. If the area is overly warm or exposed to any kind of friction it will result in a hive reaction. Benadryl helps a little bit. Primary care physician administered two steroid injections a week apart and prescribed steroid pills. This kept the itching and hives at bay until the steroids left my system. Hives immediately returned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- have a referral to dermatology
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- previously contracted covid-19 in march. No hospitalization. Tested positive and had a headache/chills for four days, then I was fine. No autoimmune diseases I've been diagnosed with.
- Andere Medikamente
- none
- Allergien
- cefaclor. Nothing else that I'm aware of.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 20.09.2021
- Impfdatum
- 17.09.2021
- Beginn
- 18.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Symptomtext
PAIN AND SWELLING TO LYMPH NODES UNDER LEFT ARM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DEPRESSION, COPD, ASTHMA
- Andere Medikamente
- QUETIAPINE, DIAZEPAM, ZOLOFT
- Allergien
- FLAGYL, TRAMADOL, HYDROCODONE
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 18.09.2021
- Impfdatum
- 16.09.2021
- Beginn
- 16.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal discomfort
Abdominal pain upper
Arthralgia
Back pain
Feeling cold
Muscle spasms
Nausea
Pain
Pyrexia
Symptomtext
Around 05 pm the pain and fever slowly started and by around 10 pm i started to have cold and hot fever, joint pain, lower back pain and followed by cramping and stomach uncomfortably and a serious pain. Medicine used for treatment: stomach such as omeprazole and anti acids, nausea tabs and pain and fever relievers but really nothing worked because of the nuasea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Nausea medicine, pain and fever relievers and digestive or stomach medicine
- Allergien
- Some foods but it happens rarely
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 17.09.2021
- Impfdatum
- 01.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Pyrexia
Symptomtext
bad chills; pretty sure he had a fever; This spontaneous case was reported by a consumer and describes the occurrence of CHILLS (bad chills) and PYREXIA (pretty sure he had a fever) in a 28-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. The patient's past medical history included COVID-19 in November 2020. On 01-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Sep-2021, the patient experienced PYREXIA (pretty sure he had a fever). On 02-Sep-2021 at 2:00 AM, the patient experienced CHILLS (bad chills). The patient was treated with PARACETAMOL (TYLENOL) for Fever, at an unspecified dose and frequency. At the time of the report, CHILLS (bad chills) and PYREXIA (pretty sure he had a fever) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No Concomitant medications were provided. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 15.09.2021
- Impfdatum
- 10.09.2021
- Beginn
- 10.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysphagia
Rash
Symptomtext
I received a rash within 5 minutes of having the vaccine. It started to spread to my back and chest. The pharmacist called the ambulance and gave me Benadryl. I went to the ER, and they kept me for 5 hours. They also gave me IV steroids. My throat also felt a little tough to swallow. I went and saw my doctor and he prescribed steroids for the rash as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Acid Reflux
- Andere Medikamente
- Pandoprozal
- Allergien
- Shrimp
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 15.09.2021
- Impfdatum
- 13.09.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Axillary pain
Symptomtext
One day after the shot a developed a large lump in my left arm bit. The lump was painful. It still has not subsided. I contacted the pharmacy and they knew not of any side affects regarding lumps in the arm pits. I subsequently looked online and read a article talking about swollen lymph nodes. I can?t believe that the people who are given the responsibility of injecting this poison into peoples bodies don?t know the current side affects or have any treatment options other then call your doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 15.09.2021
- Impfdatum
- 04.09.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Rash
Symptomtext
Large rash a week later at injection site. Spreading down arm. Taking antihistamine and cortisone cream
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma
- Andere Medikamente
- Vitamin D
- Allergien
- Yes
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 15.09.2021
- Impfdatum
- 14.09.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Dizziness
Nausea
Pain
Pain in extremity
Tinnitus
Vomiting
Symptomtext
My entire left arm started to throb at 1:00am. I then started to get nauseous and vomited. After I vomited I was walking to the couch and started to feel very light headed and my knees were starting to buckle and my ears were ringing. I felt like I was going to pass out. I laid down and went to sleep. When I woke up at 7:00 am my entire left arm was sore all the way to my wrist and the soreness was going to my shoulder down my left side all the way down to my thighs. My entire left side is sore. I am also having stomach cramps.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Non
- Vorgeschichte
- None
- Andere Medikamente
- Tri-Lo-Mili birth control, Dextroamp-Amphet ER 30 MG,
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 14.09.2021
- Impfdatum
- 09.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Eye disorder
Fatigue
Hypoacusis
Pyrexia
Tinnitus
Vertigo
Symptomtext
Fever and chills onset 7pm 24 hours after Injection. Saturday morning woke up and hearing was affected all sounds were heard as digital. Ringing in ears was significant and overal fatigue. Monday following the vaccine ? extreme vertigo and dizziness and eye sight affected with inability to transfer from looking at one object to another. Objects appeared to be flickering and vertigo persists
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- I have an mri scheduled and hearing test scheduled
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vyvanse
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 14.09.2021
- Impfdatum
- 10.09.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Sleep disorder
Symptomtext
I experienced extremely excruciating pain constantly in my right foot;on the second day of taking the second dose of Moderna! I was unable to find any relief and was unable to sleep or do anything for 3 days and nights! The pain was unbearable and the gabapentin did not help any at all. On the forth day, the pain finally subsided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Neuropathy Hypertension Chronic Back Pain
- Andere Medikamente
- Gabapentin 300 MG Cyclobenzaprine HCI 10 MG Acetaminophen-Codeine 300-60 MG Bystolic 20 MG Lisinopril-HCTZ 20-25 MG Ecotrin NSAID 81 MG Centrum Silver Multi-Vitamin
- Allergien
- None Known
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 12.09.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood creatinine
Blood glucose
Blood potassium
Blood sodium
Blood urea
Dizziness
Fatigue
Glycosylated haemoglobin
Haematocrit
Haemoglobin
Headache
Pharyngeal swelling
Platelet count
Swelling face
Swelling of eyelid
Herpes zoster
Swelling
Swollen tongue
Symptomtext
Within a few hours of receiving the vaccine the left side of my face began to swell and what I thought were hives began to appear. I also had a headache, dizziness, and fatigue. I received the vaccine on a Friday, by the following Monday the left side of my face was so swollen that my left eye was swollen shit and my vision was blurred in both eyes. I had started taking Benadryl over that weekend but it obviously wasn't helping. My tongue and throat was swelling so I went to the ER on the Monday. When I arrived at the ER my throat was almost swollen shut. They immediately began giving me medication and I was admitted to the hospital. I was given Methylprednisolone 125mg, Acyclovir 800mg, Benadryl GEq 50mg, Adrenaline GEq 0.3mg, Loratadine 10mg, Pepcid GEq 20mg, Acyclovir
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- 1,0
- Labordaten
- My hemoglobin, hematocrit, WBC count, platelet count, sodium level, potassium level, creatinine, BUN, hemoglobin A1c, and glucose level were all checked.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Obesity
- Andere Medikamente
- none
- Allergien
- Bees
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 11.09.2021
- Impfdatum
- 21.08.2021
- Beginn
- 22.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Headache
Malaise
Symptomtext
Dizziness; Not feeling well; Headache; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (Dizziness), MALAISE (Not feeling well) and HEADACHE (Headache) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. The patient's past medical history included Surgery on 27-May-2021. Concomitant products included TRAMADOL for an unknown indication. On 21-Aug-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Aug-2021, the patient experienced DIZZINESS (Dizziness), MALAISE (Not feeling well) and HEADACHE (Headache). The patient was treated with PARACETAMOL (TYLENOL) for Headache and Dizziness, at an unspecified dose and frequency. At the time of the report, DIZZINESS (Dizziness) and HEADACHE (Headache) had not resolved and MALAISE (Not feeling well) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Treatment medication: Tylenol 500mg morning and if needed two at bedtime for headache and dizziness, patient said this is not working. The patient woke up not feeling well, had relaxed since then. The patient had been, dizzy since then also headaches, the day after she got her first vaccine. The patient was still experiencing the dizziness and headaches. Company Comment: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Surgery
- Andere Medikamente
- TRAMADOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 08.09.2021
- Impfdatum
- 24.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Swelling
Symptomtext
Right side of neck is swollen; Feel lightheaded; This spontaneous case was reported by a consumer and describes the occurrence of SWELLING (Right side of neck is swollen) and DIZZINESS (Feel lightheaded) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 24-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced SWELLING (Right side of neck is swollen) and DIZZINESS (Feel lightheaded). At the time of the report, SWELLING (Right side of neck is swollen) and DIZZINESS (Feel lightheaded) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. The concomitant medication were not reported. No treatment information was mentioned by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 13.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bedridden
Body temperature
Feeling abnormal
Pyrexia
Symptomtext
I've been in bed for two days; It literally feels like my brain is splitting in two; I had 102.3?F; This spontaneous case was reported by a consumer and describes the occurrence of BEDRIDDEN (I've been in bed for two days), FEELING ABNORMAL (It literally feels like my brain is splitting in two) and PYREXIA (I had 102.3?F) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Concurrent medical conditions included Migraine. Concomitant products included SUMATRIPTAN (IMITREX [SUMATRIPTAN]) for Migraine, GABAPENTIN, LEVETIRACETAM, TAMSULOSIN, TOPIRAMATE, CELECOXIB and CHLORZOXAZONE for an unknown indication. On 13-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Aug-2021, the patient experienced BEDRIDDEN (I've been in bed for two days), FEELING ABNORMAL (It literally feels like my brain is splitting in two) and PYREXIA (I had 102.3?F). The patient was treated with ASPIRIN [ACETYLSALICYLIC ACID] for Adverse event, at an unspecified dose and frequency. On 17-Aug-2021, BEDRIDDEN (I've been in bed for two days) had resolved. At the time of the report, FEELING ABNORMAL (It literally feels like my brain is splitting in two) and PYREXIA (I had 102.3?F) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 15-Aug-2021, Body temperature: 102.3?f (High) 102.3?F. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. The reporter mentioned that he had seen to a neurologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210815; Test Name: I had 102.3?F; Result Unstructured Data: 102.3?F
- Aktuelle Erkrankungen
- Migraine
- Vorgeschichte
- -
- Andere Medikamente
- GABAPENTIN; LEVETIRACETAM; TAMSULOSIN; TOPIRAMATE; CELECOXIB; CHLORZOXAZONE; IMITREX [SUMATRIPTAN]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 01.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Headache
Pyrexia
Symptomtext
PATIENT REPORTED "BAD HEADACHE" AND FEVER OF 100.3F THE DAY FOLLOW ADMINISTRATION OF MODERNA COVID VACCINE. HE CLAIMS TO HAVE SOUGHT MEDICATION ATTENTION FROM HOSPITAL AND WAS TREATED WITH TYLENOL AND MOTRIN AND RELEASED THE SAME DAY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- PATIENT REPORT "BAD HEADACHE", AND FEVER OF 100.3F
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE KNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 31.08.2021
- Impfdatum
- 29.08.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Injection site pain
Pyrexia
Symptomtext
Extreme fatigue--commenced 20 hours after Booster injection. Fever 102.3 degrees--fever commenced somewhere between 20-22 hours after Booster injection. Took Tylenol and fever came down. Sore injection site-achy arm Slept 11am-7:30pm (hour 20-28.5 post injection) and through night (hour 29.5-37.5 post injection). FELT GREAT when I woke up!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Metastatic Appendix Cancer
- Andere Medikamente
- Lisinopril Metopolol Prilosec
- Allergien
- Sulfa Drugs Latex
- Vorherige Impfungen
- Covid Arm post Vaccine #2
- Staat
- MI
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 29.08.2021
- Impfdatum
- 17.08.2021
- Beginn
- 29.08.2021
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash papular
Rash pruritic
Symptomtext
Rash on injection arm, getting worse, red, itchy and raised. Larger pattern.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 27.08.2021
- Beginn
- 27.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Pyrexia
Symptomtext
Fever of 99.4 the evening of the vaccine; and a fever of 101.2 the next morning. Nausea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- BALT/MALT lymphoma; allergies
- Andere Medikamente
- Dentist prescribed Ibuprofen for a toothache (600 mg) three times a day on 8/26, I took it at lunch and dinne8/26 and breakfast the day of the 3rd vaccine. I completely forgot that it was a bad idea.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 19.08.2021
- Beginn
- 27.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Large rash on arm 8 days following vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypothyroidism, migraine
- Andere Medikamente
- Synthroid, Aimovig
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Exposure to SARS-CoV-2
Fatigue
Headache
Myalgia
Symptomtext
Worried because he was exposed to COVID-19; Redness; Sore arm; Light headache; Little fatigued; This spontaneous case was reported by a consumer and describes the occurrence of EXPOSURE TO SARS-COV-2 (Worried because he was exposed to COVID-19), ERYTHEMA (Redness), MYALGIA (Sore arm), HEADACHE (Light headache) and FATIGUE (Little fatigued) in a 26-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Aug-2021, the patient experienced ERYTHEMA (Redness), MYALGIA (Sore arm), HEADACHE (Light headache) and FATIGUE (Little fatigued). On an unknown date, the patient experienced EXPOSURE TO SARS-COV-2 (Worried because he was exposed to COVID-19). On 11-Aug-2021, ERYTHEMA (Redness), MYALGIA (Sore arm), HEADACHE (Light headache) and FATIGUE (Little fatigued) had resolved. At the time of the report, EXPOSURE TO SARS-COV-2 (Worried because he was exposed to COVID-19) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant treatment was provided. No treatment medication was provided. The patient was exposed to COVID-19 since the patient works in close quarters with the people and the patient's boss was tested positive for COVID-19. The patient did not had any COVID-19 symptoms but was worried about being asymptomatic and if that might affect the efficacy of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 26.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Headache
Pain in extremity
Pruritus
Symptomtext
1. Pain in arm 2. Significant itching and redness 3. headaches No medical treatment other than but benadryl jel for itching and benadryl oral
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None to date
- Aktuelle Erkrankungen
- Pre-diabetes; Menniere's Disease; Seasonal Allergies
- Vorgeschichte
- No
- Andere Medikamente
- metFORMIN HCL 500 MG; Pravastatin Sodium 40 MG; Clopidogrel 75 MG, hydroCHLOROthiazide 25 MG; Zyrtec 10MG; Alendronate Sodium 70 MG; Caltrate 600 Bone/Calcium + D Supplement; Centrum Silver Vitamin Women +50; Fish Oil 1000 mg.
- Allergien
- Penicillen; Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 26.08.2021
- Impfdatum
- 23.08.2021
- Beginn
- 24.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Noticed a rash on her arm beginning Tuesday, 8/24 at injection site. Rash began to spread to elbow and thighs by Wednesday. Thursday am, rash on other elbow and face (7:30AM). Denies any swelling of the mouth or tongue, no difficulty breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- No treatment at this time. Advised to call HCP for more direction.
- Aktuelle Erkrankungen
- GI issues, diarrhea about a month ago, over the weekend of 8/6/2021, Subsided spontaneously.
- Vorgeschichte
- None
- Andere Medikamente
- 2 pills of Famotidine -took last evening and one the day before (8/24) Cetirizine took 2 weeks ago for bee sting--took again last evening (8/25)
- Allergien
- Insect stings nickel sensitivity
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 19.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphthous ulcer
Lymphadenopathy
Pain
Rash
Symptomtext
RASH; PAIN; LYMPH NODE SWELLING; CANKER SORE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- CLL
- Vorgeschichte
- CLL
- Andere Medikamente
- lipitor, D3; C; Calcium
- Allergien
- penicillin; Sulpha
- Vorherige Impfungen
- Similar reaction after #2
- Staat
- GA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 12.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Urticaria
Symptomtext
Severe itching and hives only on the back of my leg and on the back of my right arm which lasted approximately three days. Treated with a steroid dose pack and Zyrtec.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Asthma, hypothyroidism, and depression (surrounding death of parent).
- Andere Medikamente
- Losartan, Levothyroxine, Trazadone, Sertraline, and Bupropion.
- Allergien
- Sulfa.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 18.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site pain
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Woke up to a very sore left hot to touch and swollen about 4 inches under the injection site. Later that day intense itching at the swollen site until Monday. Swelling is going down and itching is starting to go away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- multi vitamin osteo biflex baby aspirin cozaar 50 mg 1 daily
- Allergien
- none
- Vorherige Impfungen
- 10/19/18 Had Gotten the flu shot, Tdap and pheumorax all on same day so I had two put in left arm and one in the right arm. The
- Staat
- NJ
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 23.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Chromaturia
Fatigue
Jaundice
Malaise
Muscle spasms
Pyrexia
Symptomtext
Patient reports waking up the following morning with leg cramps, malaise, fatigue, feverish (subjective). Patient noted darker urine and abdominal pain starting on 8/18/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Patient will be sent to ER due to jaundice.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension and obesity
- Andere Medikamente
- Metoprolol succ 50 mg daily and Valsartan 160 mg PO daily
- Allergien
- NKDA
- Vorherige Impfungen
- Flu shot ~ 10-15 years ago
- Staat
- KY
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 21.08.2021
- Beginn
- 22.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site swelling
Lymphadenopathy
Oedema peripheral
Symptomtext
Patient reported her arm is sore and swollen at injection site. Lymph node in armpit is swollen beginning a couple of days past injection date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 22.08.2021
- Impfdatum
- 15.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Retching
Symptomtext
Patient has had extreme nausea since getting her second dose. Said she has been gagging frequently. Patient reported adverse event to the pharmacy on 8/21/21. I suggested she see her PCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- amlodipine, citalopram, metformin
- Allergien
- ciprofloxacin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 22.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Extra dose administered
Fatigue
Nausea
Pain in extremity
Pyrexia
Symptomtext
Fever and nausea developed each afternoon for 4 days vaccination. Extreme tiredness for 5 days vaccination each afternoon. Left arm sore for 4 days & red for days 2-4. I took care of symptoms myself, with Acetaminophen, ginger ale, and going to bed early.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- COPD, history of NHL
- Andere Medikamente
- Valacyclovir, vitamins, cal-mag-zinc.
- Allergien
- n/a
- Vorherige Impfungen
- 1st & 2nd Covid vaccine - mild symptoms similar to Covid booster mentioned above, but less severe.
- Staat
- SC
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 22.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Peripheral swelling
Rash
Staphylococcal infection
Symptomtext
Patient experienced arm swelling and rash 6 days after the vaccine. She went to urgent care and was advised to go to the emergency room. At the emergency room, she told she had a staff infection and was prescribed two antibiotics. her condition has resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- nka
- Vorgeschichte
- nka
- Andere Medikamente
- nka
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 22.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip blister
Lip swelling
Myalgia
Oral herpes
Sensitive skin
Pain
Symptomtext
Cold sores on lips, blisters on lips, swelling of lips. Body aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- Covid shot 8/16
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 22.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip blister
Lip swelling
Myalgia
Oral herpes
Sensitive skin
Pain
Symptomtext
Cold sores on lips, blisters on lips, swelling of lips. Body aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- Covid shot 8/16
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 21.08.2021
- Impfdatum
- 17.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Lymph node pain
Neck pain
Pain
Tenderness
Vaccination site pain
Vaccine positive rechallenge
Symptomtext
Lymph Node in neck has a painful nodule, pain radiates up neck and and radiates across clavicle area all the way to the vaccination site on left arm. Very painful to touch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Surgery to reverse temporary loop ileostomy7/12/2021
- Vorgeschichte
- Addison?s Disease, Hashimoto?s Disease, Autoimmune Gastritis, Pre-Diabetes, Hypoglycemia, Diverticulitis, Hiatal Hernia, Migraines
- Andere Medikamente
- Taken at 9:30 pm on day of vaccine: Metoprolol ER 50 mg, Famotidine 40 mg, Temazepam 15 mg, Gabapentin 300 mg, Ginger Root 550 mg, B12 1000 mcg, D3 50 mcg, Calcium/Magnesium/Zinc 1000mg/400mg/25mg,
- Allergien
- Latex
- Vorherige Impfungen
- Same reaction to second COVID-19 on 02/18/2021
- Staat
- NE
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 21.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site haemorrhage
Injection site nodule
Injection site swelling
Symptomtext
After retracting the needle, small amount of blood squirted out along with immediate knot formation (bump) about 1 inch diameter & 1 & 1/2 inch height/ raised. Patient's mother called to ask questions & said she advised patient to go to ER due to the swelling. This was his 2nd dose. I am unaware if patient actually went to doctor or received any medical care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site haemorrhage
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- unknown
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 20.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Vision blurred
Symptomtext
approximately 5 minutes after receiving vaccine patient experienced blurred vision and dizziness lasted about 15 minutes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- ASTHMA
- Vorgeschichte
- ASTHMA
- Andere Medikamente
- UNKNOWN
- Allergien
- LATEX
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 20.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site pain
Symptomtext
Patient said 16 days later, has entire arm from elbow up painful but bruise to where it looks black.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 19.08.2021
- Impfdatum
- 18.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Chills
Headache
Pain in extremity
Symptomtext
Sore arm, sore joints, headache, backache, chills
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 15.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Next morning injection site soreness and swelling, turning red later in the day and continues into day 2. Next day an increased level of fatigue and headache. Fever in the afternoon measured 99.5, 2 degrees over typical. At dinner a cold meal caused chills. Wet lungs late in the day and continues into day 2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Ulcerative Colitis, Neuropathy, Toenail fungus, Enlarged prostate, Constipation, Hiatal hernia, Hemorrhoids, Tinnitus, Sleep apnea, Vertigo, Joint pain, Headaches, Fatigue, Atherosclerosis
- Andere Medikamente
- Mesalamine, Crestor, Vitamin B complex, Vitamin K2 (MK-7)
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 13.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Symptomtext
Approximately 8 hours after my 2nd Moderna vaccination I began getting chilled and fatigued. That lasted for about 12 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- 2002 back surgery, microdiscectomy L4-L5
- Andere Medikamente
- Levothyroxine Multivitamin Lysine Vit C Vit D
- Allergien
- Iodinated Diagnostic Agents
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 11.08.2021
- Impfdatum
- 04.08.2021
- Beginn
- 04.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Malaise
Nasal congestion
Paranasal sinus hypersecretion
SARS-CoV-2 test positive
Symptomtext
Patient got first Moderna vaccine 5/24/2021 and waited to get second one due to malaise. Patient went to Store last night and got the second Moderna vaccine. Patient had possible exposure 1 week ago. Did rapid home Covid test 8/3/2021 and it was negative. Patient took another rapid home Covid test 8/5 and the result was positive. Had positive COVID19 NAA swab in office 8/6. In retrospect, she thinks her symptoms started 8/3/2021. She chalked them up to allergies. Her symptoms include nasal congestion, nasal discharge, and mild cough. She denies SOB, fever, chest pain, and wheezing. She has a h/o asthma and asks about using Albuterol. I concur that she can use it QID to keep her asthma In check. She got her first COVID19 vaccine in 5/2021 but waited until August for the second as the first one caused extreme malaise and she did not want to risk missing work.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 27.06.2023
- Impfdatum
- 18.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Blindness unilateral
Cardiac monitoring
Central nervous system lesion
Laboratory test abnormal
Scan with contrast abnormal
Speech disorder
Unevaluable event
Symptomtext
She was losing her balance and some of her speech was not coming out right. She woke up and her right eye vision was completely black and is blind in the right eye. Went to the doctor for her eye, they did a run tests and the tests showed that the frontal lobe of her brain showed lesions. They saw it by using contrast. They said it could be early dementia or Alzheimer's or MS. They gave her a heart monitor. She also can put a large magnet on her arm and chest and it stays.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Balance disorder
- Hospital-Tage
- -
- Labordaten
- Several, names unkown.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Unknown
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 25.04.2023
- Impfdatum
- 27.09.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
Brain fog
Symptomtext
My sense of smell is almost nonexistent. I have brain fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anosmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Post liver transplant
- Vorgeschichte
- Diabetes mellitus
- Andere Medikamente
- Calcium/Vit D, Carvedilol 25mg, Fenofibrate 48mg, FeSO4 5gr, Fish Oil 1200mg, Furosemide 40mg, Glipizide 5mg, Hydralazine 50mg, Jardiance 25mg, Metformin 1000mg, Mounjaro, Pantoprazole 40mg, Prednisone 5mg, Rosuvastatin 20mg, Slow Mag, Tacr
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 5,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 15.11.2022
- Beginn
- 25.01.2023
- Tage bis Beginn
- 71,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
COVID dose is incorrect/ inconsistent with the age of the pediatric client.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None. Patient did not have a reaction
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- F
- Eingang
- 14.11.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse reaction; Got expired vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Got expired vaccine) and NO ADVERSE EVENT (No adverse reaction) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Got expired vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse reaction). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Got expired vaccine) and NO ADVERSE EVENT (No adverse reaction) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse reaction) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Got expired vaccine). Concomitant medication was not reported. Patient and her husband received expired vaccine. They did not experience any side effects. Treatment details were not reported. This case was linked to MODERNATX, INC.-MOD-2022-662400 (E2B Linked Report).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 12.11.2022
- Impfdatum
- 01.01.2021
- Beginn
- 01.05.2022
- Tage bis Beginn
- 485,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ankylosing spondylitis
Biopsy kidney
Blood test abnormal
Chronic kidney disease
Glomerulosclerosis
Nephritis
Renal tubular atrophy
Ultrasound kidney abnormal
Symptomtext
Diagnosed with stage 4 chronic kidney disease in May 2022. No prior history of kidney disease. Diagnosed with ankolosing spondylitis in September 2022, no prior history of autoimmune arthritis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ankylosing spondylitis
- Hospital-Tage
- -
- Labordaten
- Emergency room visit and overnight hospital stay May 2022 showed stage 3 CKD. Renal ultrasound, blood work confirmed. By October 2022, CKD had progressed to stage 4. Autoimmune blood tests and plethora of other blood testing confirmed diagnosis of CKD. RIGHT kidney biopsies in Oct. 2022 showed global glomerulosclerosis, nephritis and tubular atrophy. I had no prior history of kidney diseases prior to first vaccine in 2021.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hasimoto?s
- Andere Medikamente
- Adderall, vybriid, lunesta, Xanax
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 12.11.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; expired dose administered (Expiration Date: Oct 11, 2021 and January 13, 2022); This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired dose administered (Expiration Date: Oct 11, 2021 and January 13, 2022)) and NO ADVERSE EVENT (No adverse event) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 prophylaxis. None allergies to medications, food and other products. Patient never diagnosed with or tested positive for COVID-19. Patient had no acute illness at the time of vaccination and up to one month before. Patient had no chronic or longstanding health conditions. On 22-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired dose administered (Expiration Date: Oct 11, 2021 and January 13, 2022)). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired dose administered (Expiration Date: Oct 11, 2021 and January 13, 2022)) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered EXPIRED PRODUCT ADMINISTERED (expired dose administered (Expiration Date: Oct 11, 2021 and January 13, 2022)) and NO ADVERSE EVENT (No adverse event) to be not related. No concomitant information was reported. It was reported that No adverse reaction reported. Patient didn't experience any side effects. The event did not cause the patient to seek medical care. There were no other potential causes. Patient had not experienced similar event in the past. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: None allergies to medications, food and other products. Patient never diagnosed with or tested positive for COVID-19. Patient had no acute illness at the time of vaccination and up to one month before. Patient had no chronic or longstanding health conditions.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 08.10.2022
- Impfdatum
- 13.09.2021
- Beginn
- 06.10.2022
- Tage bis Beginn
- 388,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case after 3 vaccines Moderna 3/3/21 NO LOT #; 8/12/21 Moderna Lot# 050C21A ; Moderna 9/13/21 Lot# 049E21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 25.09.2022
- Impfdatum
- 18.09.2020
- Beginn
- 06.06.2022
- Tage bis Beginn
- 626,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
Diagnosed with Covid 19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Tested positive on antigen test June 6 2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 17.08.2021
- Beginn
- 12.09.2022
- Tage bis Beginn
- 391,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 15.08.2022
- Impfdatum
- 01.09.2021
- Beginn
- 14.08.2022
- Tage bis Beginn
- 347,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough case dose 1 Moderna 6/11/21 050C21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ 8/14/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 09.07.2022
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Fibrin D dimer normal
Full blood count normal
Goitre
Increased tendency to bruise
Lymphadenopathy
Metabolic function test normal
Swelling
Thyroid function test normal
Symptomtext
AXILLARY ADENOPATHY, NECK SWELLING, THYROID ENLARGEMENT, PROGRESSIVE WITH SECOND DOSE, LONG-LASTING, EASY BRUISING
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fibrin D dimer normal
- Hospital-Tage
- -
- Labordaten
- CMP, CBC, THRYROID PANEL, D-DIMER, ALL WNL
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 21.10.2021
- Beginn
- 02.07.2022
- Tage bis Beginn
- 254,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Exposure during pregnancy
Normal labour
SARS-CoV-2 test positive
Streptococcal infection
Streptococcus test positive
Uterine contractions during pregnancy
Symptomtext
HISTORY OF PRESENT ILLNESS: This patient is a gravida 4, para 2-0-1-2 female with an EDC of 06/30/2022 by LMP equal to ultrasound at 6 weeks and 3 days. She is currently at 40 weeks and 2 days today. She presents today for a spontaneous onset of labor. She had been found to be 3 cm at the office on Wednesday. She now comes in with regular pattern of contractions. Her history has been complicated by recent COVID virus positive testing. She also has had positive group B strep.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- REVIEW OF SYSTEMS: She denies any active cardiac, pulmonary or GI complaints. Despite having tested positive for the COVID, she is not currently having any symptoms. Her positive test was on 06/24/2022. She is now 8 days past that. Her COVID test does remain positive.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- obesity
- Andere Medikamente
- unknown
- Allergien
- Flonase
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 01.07.2022
- Impfdatum
- 25.08.2021
- Beginn
- 28.06.2022
- Tage bis Beginn
- 307,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated with booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid antigen 6/28/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- CLL, Waldenstroms, GERD, nephrolithiasis, HLD, HFpEF (EF 50-55% with G2DD), urinary retention
- Andere Medikamente
- unknown
- Allergien
- Sulfamethoxazole, trimethoprim, ampicillin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 24.06.2022
- Impfdatum
- 18.09.2021
- Beginn
- 23.06.2022
- Tage bis Beginn
- 278,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 18.09.2021
- Beginn
- 13.06.2022
- Tage bis Beginn
- 268,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.04.2022
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- 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
Have received an expired dose; This spontaneous case was reported by a consumer and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Have received an expired dose) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Have received an expired dose). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Have received an expired dose) outcome was unknown. No concomitant medications were reported. Patient received second dose of Moderna vaccine on 29-Nov-2021 with lot number 049E21A and expiry date 11-Oct-2021. No treatment medications were reported. This case was linked to MOD-2022-547112 (Patient Link). Reporter did not allow further contact Most recent FOLLOW-UP information incorporated above includes: On 22-Apr-2022: No new information received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 19.03.2022
- Impfdatum
- 30.09.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 55,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Biopsy skin normal
Limb mass
Skin lesion
Skin mass
Symptomtext
Between Thanksgiving and Christmas 2021, a growth developed on my left forearm above the wrist. It kept growing until it stuck up 1/4th inches from the surrounding tissue and had a subcutaneous knot about 1/4th inches circumference. I was seen at 9:00 am on 1-5-2022 by Dr. who immediately scheduled an appointment for me with a dermotologist for 11:00 that same day. Dermatologist, initially diagnosed the growth as a keratoacanthoma and immediately biopsied it and sent it for examination. Results 2 days later came back benign as a skin lesion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy skin normal
- Hospital-Tage
- -
- Labordaten
- Biopsy of growth and surrounding tissue. Benign skin lesion.
- Aktuelle Erkrankungen
- only typical air borne allergy symptoms for that time of year
- Vorgeschichte
- Type 2 diabetisis, obesety
- Andere Medikamente
- Victosa, metformin ER, simvastatin, spironolactone, 81 mg Aspirin, claratin, citracal + D3, B12
- Allergien
- air borne pollens, coconut, drugs with synthetic codeines like darvocet, celebrex, tylenol with codience, myconosole, tramadol, etc.
- Vorherige Impfungen
- Headache for 5 days beginning within 1 hour of 2nd dose of Moderna on 03/01/2021. I was 69 at the time of the injection.
- Staat
- NJ
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
COVID19 infection (positive PCR) requiring doctor visit
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- PCR test 2/3/22 positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blindness unilateral
Optic ischaemic neuropathy
Symptomtext
stroke in the optic nerve- blindness in the right eye
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blindness unilateral
- Hospital-Tage
- -
- Labordaten
- currently on Steroids
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Managed Heart condition
- Andere Medikamente
- cholesterol, blood thinners
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 25.09.2021
- Beginn
- 25.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Tinnitus
Symptomtext
Severe Tinnitus
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- Blood tests 1/17/22 Audiogram scheduled for 1/24/22 MRI in process of scheduling
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- 0.25 mg Metroprolol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 10.12.2021
- Impfdatum
- 19.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Vaccination error
Symptomtext
This is not an adverse event. It was a vaccination error. The patient was given the Moderna vaccinations 21 days apart instead of the approved 28 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 09.12.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
they administered approximately 100 doses of expired vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (they administered approximately 100 doses of expired vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In November 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (they administered approximately 100 doses of expired vaccine). In November 2021, EXPIRED PRODUCT ADMINISTERED (they administered approximately 100 doses of expired vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The reporter who was a pharmacist was calling to report that about 100 patients received expired booster Moderna COVID-19 vaccine from 09-Nov-2021 through 21-Nov-2021 with expiry date 11-Oct-2021. Nobody reported side effects. They just discovered the error and reported to VAERS already. The reporter does not have information on the date the vial was initially stored in the refrigerator and the Date and time vial was first punctured was unknown. The vial was stored in the fridge post puncture and the vial didn't undergo any temperature excursions. Reportedly, the total amount of time the vial was exposed to room temperature range 8? to 25?C= 46? to 77?F was unknown. The vaccines were stored in the freezer and used as soon as they were thawed. No Concomitant product use was reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product temperature excursion issue
Symptomtext
potential administration of expired vaccine/ administration of expired vaccine; temperature excursions; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (potential administration of expired vaccine/ administration of expired vaccine) and PRODUCT TEMPERATURE EXCURSION ISSUE (temperature excursions) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (potential administration of expired vaccine/ administration of expired vaccine) and PRODUCT TEMPERATURE EXCURSION ISSUE (temperature excursions). On 05-Nov-2021, EXPIRED PRODUCT ADMINISTERED (potential administration of expired vaccine/ administration of expired vaccine) and PRODUCT TEMPERATURE EXCURSION ISSUE (temperature excursions) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that, the vial were stored in the refrigerator on 08-Oct-2021 and 05-Nov-2021. Also, it was reported that, both the vials were stored in an ultracold freezer since 08-Sep-2021. The second vial was moved from ultracold freezer to normal freezer on 26-Oct-2021. The vials stayed within recommended frozen storage temperatures until day of administration (05-Nov-2021). Most recent FOLLOW-UP information incorporated above includes: On 02-Dec-2021: Follow-up received includes updated lot number, additional event, drug start date, expiry date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in system is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Arthritis, chronic kidney disease, GERD, diverticulitis, oseteoarthritis
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA) (modernatx.com). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Anemia, HTN, chronic kidney disease, coronary artery disease, hyperkalemia, hyperlipidemia
- Andere Medikamente
- Unknown
- Allergien
- Fish oil
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in VAOS is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA) (modernatx.com). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Atrial flutters, HDL deficiency, hyperkalemia, hypertriglycedemia
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in VAOS is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA) (modernatx.com). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Atrial fibrillation, HTN, chronic kidney disease, GERD
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup|Moderna COVID-19 Vaccine. Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- HTN, hyperlipidemia, diabetes
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in database is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Polyoythemia, Hyperplasia of prostate, elevated blood
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in VAOS is 12/31/2069. To find the expiration date, look up expiration date tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine. Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Chronic kidney disease, osteoarthritis, gout, hyperlipidemia
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in VAOS is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA) (modernatx.com). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Asthma
- Vorgeschichte
- Chest pain, HTN, Hypothyroidism
- Andere Medikamente
- Unknown
- Allergien
- Coptisone
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in VAOS is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hyperlipidemia, Osteoporosis
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- HTN
- Andere Medikamente
- Unknown
- Allergien
- Penicillin, Latex
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna booster vaccine administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected between 8-10 business days. Expiration date currently not printed on the vaccine vial or carton. Vaccine expiration date listed in the database lookup tool is 12/31/2069. Patient contacted on 12/4/2021. No adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hyperlipidemia, osteoarthritis, prediabetes
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
No adverse event
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in database is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Diabetes, HTN, venous insufficiency, overweight
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Moderna booster vaccine administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected between 8-10 business days. Expiration date currently not printed on the vaccine vial or carton. Vaccine expiration date listed in database lookup tool is 12/31/2069. Patient contacted on 12/4/2021 and 12/6/2021, unsuccessful attempts to speak with patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Chronic kidney disease, diabetes, HTN
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
No adverse event
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in database is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed is 12/31/2069. To find the expiration date, "look up expiration date" tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine. Patient contacted on 12/4/2021 and no adverse effects reported.
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
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna booster vaccine administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected 8-10 business days. Expiration date currently not printed on the vaccine vial or carton. Vaccine expiration date listed in database lookup tool is 12/31/2069. Patient contacted on 12/4/2021. No adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hyperlipidemia, HTN, hypotension, hypothyroidism
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Moderna vaccine booster administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected between 8-10 business days. Expiration date currently not printed on the vaccine vial or carton. Vaccine expiration date listed in the database lookup tool is 12/31/2069. Patient contacted on 12/4/2021 and 12/6/2021, unsuccessful attempts to contact patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- HTN
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine . Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA) Patient contacted on 12/4/2021 and no adverse effects reported.
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
- -
- Staat
- TX
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in VAOS is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA) (modernatx.com). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Bradycardia, GERD, Diabetes, Overweight, Enlarged prostate
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in database is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Hyperlipidemia, GI reflux, Vertigo
- Vorgeschichte
- Hyperlipidemia, GI reflux, Vertigo
- Andere Medikamente
- Unknown
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from (PRIVACY) Moderna COVID-19 Vaccine (website:PRIVACY). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hypothyroid, overweight
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna booster vaccine booster administered 11/5/2021 with an expiration date of 10/11/2021. Inquiry submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected between 8-10 business days. Expiration date currently not printed on the vaccine vial or carton. Vaccine expiration date listed in the database lookup tool is 12/31/2069. Patient contacted on 12/4/2021. No adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna booster vaccine administered 11/5/2021 with an expiration date of 10/11/2021. Inquiry submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected between 8-10 business days. Expiration date currently not printed on the vaccine vial or carton. Vaccine expiration date listed in the database lookup tool is 12/31/2069. Patient contacted on 12/4/2021. No adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA) Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
No adverse event
Symptomtext
Moderna booster vaccine administered 11/5/2021 with an expiration date of 10/11/2021. Inquiry submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected between 8-10 business days. Expiration date currently not printed on the vaccine vial or carton. Vaccine expiration date listed in the database lookup tool is 12/31/2069. Patient contacted on 12/4/2021. No adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Iodine
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in database is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA) (modernatx.com). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
No adverse event
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed in VAOS is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA) (modernatx.com). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- HTN
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Moderna vaccine booster was administered on 11/5/2021 with an expiration date of 10/11/2021. Inquiry has been submitted to Moderna requesting validation of vaccine potency. A response from Moderna is expected to be received between 8-10 business days. Expiration date is currently not printed on the vaccine vial or carton and vaccine expiration date listed is 12/31/2069. To find the expiration date, ?look up expiration date? tool is to be used from Vial Expiration Date Lookup | Moderna COVID-19 Vaccine (EUA) (modernatx.com). Patient contacted on 12/4/2021 and no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.12.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine.) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine.). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment medications were provided. The storage of refrigerator thawed and given on the same date but never stored in refrigerator. No vial had undergone any temperature excursions. There were no adverse reactions to the vaccine as reported by the patient. This case was linked to MOD-2021-391439 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow up received contains Non significant information,added secondary reporter information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments.No concomitant and treatment medications were reported by reporter.Most recent FOLLOW-UP information incorporated above includes:On 19-Nov-2021: Follow Up received on 19-Nov-2021 (Second reporter Information is updated.)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vials were used to provide 38 doses; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vials were used to provide 38 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vials were used to provide 38 doses). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vials were used to provide 38 doses) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was reported. No treatment medication information was reported. It was reported that no excursion occurred. The Moderna vials were taken out of the freezer, thawed and administered as instructed. No delays occurred in administration of Moderna vaccine. On 12 Nov 2021 all vaccines were administered within 2 hrs. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow-up received includes updated Second reporter Information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 29.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. No vial went any temperature excursions. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: In additional information included suspect administration date were updated. On 19-Nov-2021: Follow-up information included about patients details. On 19-Nov-2021: Significant FU appended (Second reporter Information is updated).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 29.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 01-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. No excursion occurred. The Moderna vials were taken out of the freezer, thawed and administered as instructed. No delays occurred in administration of Moderna vaccine. On 01Nov2021, all vaccines were administered within 4-5 hours. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow-up received includes updated Second reporter Information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 27.11.2021
- Impfdatum
- 09.10.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 49,0
- 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
No reported adverse event Inadvertently administered vaccine, unauthorized age group
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- unknown
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. No vial went any temperature excursions. It was reported that, there are no adverse reactions to the vaccine. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow up document contains non significant information, Second reporter Information added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vials were used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vials were used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vials were used). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vials were used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment medications were reported. No vial had undergone any temperature excursions. There were no adverse reactions to the vaccine as reported by the patient. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow up received on 19-Nov-21, included secondary reporter details
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vaccine administered; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine administered) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine administered). On 05-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vaccine administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. No vial had undergone any temperature excursions. There were no adverse reactions to the vaccine as reported by the patient. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow up added new reporter information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 05-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment medications were provided. No vial went any temperature excursions. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow Up Appended (Second reporter Information)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 05-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications information was reported. No treatment medications were provided. No vial went any temperature excursions. There are no adverse reactions to the vaccine reported. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow-up received contains non-significant information- Added second reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vials were used to provide 38 doses; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. No vial went any temperature excursions. On 12-Nov-2021, all vaccines were administered within 2 hours. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. Till 19-Nov-2021, there were no adverse reactions to the vaccine. As of 19 Nov 2021, there were no adverse reactions to the vaccine reported by the list below. We spoke with some that received the vaccine during these dates and some identified common side effects after the vaccine (ex: sore arm, etc.) and only lasted for a few hours but no more than 24 hours for 1st dose, 2nd dose and Booster. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 18-Nov-2021: The additional information included suspect administration date. On 19-Nov-2021: Follow-up information included about patients details On 19-Nov-2021: Significant FU appended (Second reporter Information was updated)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. vaccine expiration date was 11-OCT-2021. No vial went any temperature excursions. vaccine was administered within 2 hrs. No adverse reactions to the vaccine reported. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Non Significant FU : Secondary reporter Information is updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 27.11.2021
- Impfdatum
- 24.10.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a 72-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A,) for COVID-19 vaccination. No Medical History information was reported. On 24-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 24-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 24-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitants and treatment medications reported. This case was linked to MOD-2021-363223 (Patient Link). Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine used). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. No treatment medication were provided Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow Up received contains no significant information.; Sender's Comments: Case is non-serious no CC needed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vials were used to provide 38 doses; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vials were used to provide 38 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vials were used to provide 38 doses). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vials were used to provide 38 doses) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. No vial went any temperature excursions. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Non Significant Follow Up Appended with Second reporter Information in case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 05-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. No vial went any temperature excursions. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow up received, Reporter information updated, Dose administration details updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vials were used to provide 38 doses; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment medication was reported. No vial went any temperature excursions and it was reported that, there were no adverse reactions to the vaccine. Company comment- This is a spontaneous case concerning a patient of unknown age and gender with no relevant medical history, who experienced the non serious event of expired product administered for mRNA-1273 vaccine with lot number 049E21A. The event expired product administered occurred right after the first dose of mRNA-1273 vaccine administration, the administered mRNA-1273 vaccine was 32 days past its manufacturer date of expiry (manufacturer date of expiry: 11 October 2021, date of mRNA-1273 vaccine administration: 12 November 2021). The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow Up was received contains non significant information, added secondary reporter details.; Sender's Comments: This is a spontaneous case concerning a patient of unknown age and gender with no relevant medical history, who experienced the non serious event of expired product administered for mRNA-1273 vaccine with lot number 049E21A. The event expired product administered occurred right after the first dose of mRNA-1273 vaccine administration, the administered mRNA-1273 vaccine was 32 days past its manufacturer date of expiry (manufacturer date of expiry: 11 October 2021, date of mRNA-1273 vaccine administration: 12 November 2021). The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine.) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine.). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. No vial had undergone any temperature excursions. There were no adverse reactions to the vaccine as reported by the patient. Reported some that received the vaccine during dates given and some identified common side effects after the vaccine (ex: sore arm, etc.) and only lasted for a few hours but no more than 24 hours for 1st dose, 2nd dose and Booster. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow up received contains Non significant information. Added: secondary reporter details.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. No vial went any temperature excursions. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow up received added second reporter information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 11-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route), the reporter did not provide any causality assessments. No concomitant medication was reported. No treatment information was provided. No vial went any temperature excursions. there was no adverse reactions to the patient Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow up added second reporter details
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vials were used to provide 38 doses; This spontaneous case was reported by an other health care professional and describes the occurrence of PAIN IN EXTREMITY (Sore arm), VACCINATION COMPLICATION (some identified common side effects after the vaccine (ex: sore arm, etc.)) and EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses). In November 2021, the patient experienced PAIN IN EXTREMITY (Sore arm) and VACCINATION COMPLICATION (some identified common side effects after the vaccine (ex: sore arm, etc.)). On 05-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) had resolved. In November 2021, PAIN IN EXTREMITY (Sore arm) and VACCINATION COMPLICATION (some identified common side effects after the vaccine (ex: sore arm, etc.)) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. No vial went any temperature excursions. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. Till 19-Nov-2021, there were no adverse reactions to the vaccine. As of 19 Nov 2021, there were no adverse reactions to the vaccine reported by the list below. We spoke with some that received the vaccine during these dates and some identified common side effects after the vaccine (ex: sore arm, etc.) and only lasted for a few hours but no more than 24 hours for 1st dose, 2nd dose and Booster. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 18-Nov-2021: The additional information included suspect administration date. On 19-Nov-2021: Follow-up information included about patients details On 19-Nov-2021: Significant FU appended (Second reporter Information was updated)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vials were used to provide 38 doses; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vials were used to provide 38 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vials were used to provide 38 doses). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vials were used to provide 38 doses) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. No vial went any temperature excursions. On 12-NOV , all vaccines were administered within 2 hrs. It was reported that, there are no adverse reactions to the vaccine. This is a spontaneous case concerning a patient of unknown age and gender with no relevant medical history, who experienced the non serious event of expired product administered for mRNA-1273 vaccine with lot number 049E21A. The event expired product administered occurred right after the third dose of mRNA-1273 vaccine administration, the administered mRNA-1273 vaccine was 32 days past its manufacturer date of expiry (manufacturer date of expiry: 11 October 2021, date of mRNA-1273 vaccine administration: 12 November 2021). The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow up received contains secondary reporter as non-significant information.; Sender's Comments: This is a spontaneous case concerning a patient of unknown age and gender with no relevant medical history, who experienced the non serious event of expired product administered for mRNA-1273 vaccine with lot number 049E21A. The event expired product administered occurred right after the third dose of mRNA-1273 vaccine administration, the administered mRNA-1273 vaccine was 32 days past its manufacturer date of expiry (manufacturer date of expiry: 11 October 2021, date of mRNA-1273 vaccine administration: 12 November 2021). The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine.) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine.). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses of of the Moderna Covid-19 Vaccine.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter Treatment information was not provided vaccine expiration date was 11-OCT-2021. No vial went any temperature excursions. vaccine was administered within 2 hrs. No adverse reactions to the vaccine reported. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: non significant follow up-Added Secondary reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 05-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. No vial went any temperature excursions. On 11/5 all vaccines were administered within 3 hours Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow-up received, Secondary reporter Information was added; Sender's Comments: Non-serious case.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 11-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. No vial went any temperature excursions. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Significant FU appended contains Second reporter Information is updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 01-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. No vial went any temperature excursions. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Significant FU appended (Second reporter Information is updated)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 26.11.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired Moderna COVID-19 Vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Moderna COVID-19 Vaccine) in a 41-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Moderna COVID-19 Vaccine). On 23-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Expired Moderna COVID-19 Vaccine) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment details were provided. This case was linked to MOD-2021-363223 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow up received included patient demographics, vaccine information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vials were used to provide 38 doses; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses). On 11-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. It was reported some that received the vaccine during dates given and some identified common side effects after the vaccine (ex: sore arm, etc.) and only lasted for a few hours but no more than 24 hours for 1st dose, 2nd dose and Booster.Reporter stated that no excursion had occurred and the Moderna vials were taken out of the freezer. It was also reported that on 11-Nov-2021 all vaccines were administered within 1 hour. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Non Significant FU appended with Second reporter Information updated in case.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by a health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route), the reporter did not provide any causality assessments. Date the vial was initially stored in the refrigerator: thawed & given on same date, never stored in refrigerator No concomitant medications were provided. No treatment medications were provided Reported some that received the vaccine during dates given and some identified common side effects after the vaccine (ex: sore arm, etc.) and only lasted for a few hours but no more than 24 hours for 1st dose, 2nd dose and Booster. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Follow Up received and a new reporter Information added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported No treatment medications were reported. Reported some that received the vaccine during dates given and some identified common side effects after the vaccine (ex: sore arm, etc.) and only lasted for a few hours but no more than 24 hours for 1st dose, 2nd dose and Booster. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Non Significant Follow Up Appended and Second reporter Information is updated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 26.11.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 23-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. Treatment information was not provided by the reporter. This case was linked to MOD-2021-363223 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Patient details was added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 07.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
6 patients received expired moderna vaccine booster doses; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (6 patients received expired moderna vaccine booster doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (6 patients received expired moderna vaccine booster doses). On 07-Nov-2021, EXPIRED PRODUCT ADMINISTERED (6 patients received expired moderna vaccine booster doses) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Reporter reported, Date the vial was initially stored in the refrigerator: 07-Nov-2021. No relevant concomitant medications were reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 05-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. No treatment information was provided. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. No vial went any temperature excursions. Additionally, as of 19-Nov-2021, no adverse reactions to the vaccine reported. Most recent FOLLOW-UP information incorporated above includes: On 18-Nov-2021: In additional information included suspect administration date were updated On 19-Nov-2021: Follow-up information included about patients details On 19-Nov-2021: Correct information about the dose administration received. On 22-Nov-2021: Follow up received with no new information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- M
- Eingang
- 25.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vials were used (1st dose); This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vials were used (1st dose)) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vials were used (1st dose)). On 27-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Expired vials were used (1st dose)) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medication was provided. No vial had undergone any temperature excursions. There were no adverse reactions to the vaccine as reported. Most recent FOLLOW-UP information incorporated above includes: On 18-Nov-2021: Follow up received : Product Administration dates were updated. On 19-Nov-2021: Follow up received : Patient's first name and last name updated On 19-Nov-2021: Follow up received : reporter Information updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 25.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vials were used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vials were used) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vials were used). On 05-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired vials were used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided by the reporter. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Non-Significant follow up appended secondary reporter information added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 25.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vials were used to provide 38 doses; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired vials were used to provide 38 doses) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. No vial went any temperature excursions. On 12-Nov-2021, all vaccines were administered within 2 hours. Some of patient received booster dose on 1-Nov-2021, 05-Nov-2021, 11-Nov-2021 and 12-Nov-2021. Till 19-Nov-2021, there were no adverse reactions to the vaccine. As of 19 Nov 2021, there were no adverse reactions to the vaccine reported by the list below. We spoke with some that received the vaccine during these dates and some identified common side effects after the vaccine (ex: sore arm, etc.) and only lasted for a few hours but no more than 24 hours for 1st dose, 2nd dose and Booster. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 18-Nov-2021: Follow up information received on 18 Nov 2021 included suspect administration date. On 19-Nov-2021: Follow-up information received on 19 Nov 2021 included about patients details On 19-Nov-2021: Significant Follow up received on 19 Nov 2021 appended (Second reporter Information was updated)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 25.11.2021
- Impfdatum
- 24.10.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired Moderna COVID19 Vaccine/ Inadvertently used a lot that looks like it had expired; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Moderna COVID19 Vaccine/ Inadvertently used a lot that looks like it had expired) in a 28-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 24-Oct-2021 at 2:53 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 24-Oct-2021 at 2:53 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Moderna COVID19 Vaccine/ Inadvertently used a lot that looks like it had expired). On 24-Oct-2021 at 2:53 PM, EXPIRED PRODUCT ADMINISTERED (Expired Moderna COVID19 Vaccine/ Inadvertently used a lot that looks like it had expired) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant drugs were reported. No treatment drugs were reported. Seven patients were inadvertantly administered with booster shots, Moderna, lot 049E21A. None of the seven patients had reported any adverse reactions till 11/19/2021. Did not have any information on their past corona history. This case was linked to MOD-2021-363223 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Significant follow-up received and included patient's details (initials, DOB, age, gender, race), Suspect's details (start date, time, anatomical location, route of administration, dose number, expiration date), vaccine facility information, event onset date and stop date were updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 25.11.2021
- Impfdatum
- 24.10.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a 66-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 24-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 24-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 24-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. Treatment information was not provided by the reporter. The reporter stated that the vial was frozen this whole time and was thawed out one day before use. Date the vails was initially stored in the refrigerator 23 Oct 2021 and 24 Oct 2021. This case was linked to MOD-2021-363223 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 24.11.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a 71-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination.No Medical History information was reported. On 23-Oct-2021 at 1:48 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Oct-2021 at 1:48 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 23-Oct-2021 at 1:48 PM, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. Not Provided.For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments.Concomitant medication details were not reported by the reporter.Treatment details was not reported by the reporter. It was reported that none of the patients have reported any adverse reactions as of 19-NOV-2021.This case was linked to MOD-2021-363223 (Patient Link).Most recent FOLLOW-UP information incorporated above includes: On 19-Nov-2021: Initial additional document received contains patient demographics and vaccine information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 24.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired dose of the vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported.On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired dose of the vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received expired dose of the vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments.No concomitant medications were reported. Treatment information was not provided.Expiry date of the vaccine is on 11-Oct-2021. As of 15-Nov-2021, at least 30 patients were administered by this expired vaccine. It was reported that the no Adverse events occurred after administration of any of the vaccines that were reported as being expired.Most recent FOLLOW-UP information incorporated above includes:On 17-Nov-2021: Follow up received. Updated Batch/lot number and expiration date of Suspect and updated Action taken, De challenge as Not Applicable, Updated event outcome as Recovered/ Resolved. Updated company causality as Not Applicable from Initial version.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vials were used (Second Dose); Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vials were used (Second Dose)) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vials were used (Second Dose)). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired vials were used (Second Dose)) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 10.09.2021
- Beginn
- 14.09.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Haemorrhage
Heavy menstrual bleeding
Symptomtext
I have not had a menstrual period since 3/2021 due to taking birth control without placebo, which was prescribed by my doctor. Several days after I received the vaccine, I began to have a severe, heavy period / menstrual bleeding which was not normal or part of my regular cycle. The bleeding was significant?I changed a pad every several hours and bled for 3 weeks straight at this rate. I did not have money to go to the doctor about this and it eventually stopped. Now, every time I have sex with my husband, I bleed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Haemorrhage
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Blisovi 1/20
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
5 Doses administered past the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (5 Doses administered past the expiration date) in a 60-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 27-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (5 Doses administered past the expiration date). On 27-Oct-2021, EXPIRED PRODUCT ADMINISTERED (5 Doses administered past the expiration date) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment information was provided. This case was linked to MOD-2021-380857 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
5 doses administered past the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (5 doses administered past the expiration date) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 27-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (5 doses administered past the expiration date). On 27-Oct-2021, EXPIRED PRODUCT ADMINISTERED (5 doses administered past the expiration date) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not provided. Treatment information was not provided. On 27-Oct-2021, the vials were taken out of freezer and were thawed and administered on the same day. Vials were stored properly, and no temperature excursion issue was involved with the vials.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
5 doses were administered (all booster doses of 0.25 ml) from expired vials; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (5 doses were administered (all booster doses of 0.25 ml) from expired vials) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 27-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (5 doses were administered (all booster doses of 0.25 ml) from expired vials). On 27-Oct-2021, EXPIRED PRODUCT ADMINISTERED (5 doses were administered (all booster doses of 0.25 ml) from expired vials) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medication were reported. No Treatment information was provided by the reporter. It was reported that Vials were taken out of freezer on 27Oct2021. Vials were thawed and administered on the same day.Vials were stored properly, no temperature excursions involved. This case was linked to MOD-2021-380859, MOD-2021-380860, MOD-2021-380834, MOD-2021-380857 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
5 Doses administered past the expiration date/5 doses were administered (all booster doses of 0.25 ml) from expired vials; This spontaneous case was reported by a health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (5 Doses administered past the expiration date/5 doses were administered (all booster doses of 0.25 ml) from expired vials) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 27-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (5 Doses administered past the expiration date/5 doses were administered (all booster doses of 0.25 ml) from expired vials). On 27-Oct-2021, EXPIRED PRODUCT ADMINISTERED (5 Doses administered past the expiration date/5 doses were administered (all booster doses of 0.25 ml) from expired vials) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications provided. No treatment medications provided. Vials were taken out of freezer on 27 Oct 2021. Vials were thawed and administered on the same day. Vials were stored properly, no temperature excursions involved. This case was linked to MOD-2021-380859, MOD-2021-380858, MOD-2021-380834, MOD-2021-380860 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
5 Doses administered past the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (5 Doses administered past the expiration date) in a 23-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 27-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (5 Doses administered past the expiration date). On 27-Oct-2021, EXPIRED PRODUCT ADMINISTERED (5 Doses administered past the expiration date) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided No treatment received by the patient. It was reported that vials were taken out of freezer on 27Oct2021. Vials were thawed and administered on the same day and vials were stored properly, no temperature excursions involved. This case was linked to MOD-2021-380857, MOD-2021-380858 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after expiry date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after expiry date) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after expiry date). On 29-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after expiry date) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant product was provided by the reporter. On 15-Apr-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Inappropriate schedule of product administration
Symptomtext
Patient received vaccine after expiry date; Inappropriate schedule of vaccine administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after expiry date) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) in a 69-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Previously administered products included for an unreported indication: PFIZER BIONTECH COVID-19 VACCINE on 30-Mar-2021 and PFIZER BIONTECH COVID-19 VACCINE. On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after expiry date) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). On 29-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after expiry date) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications were not provided. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after expiry date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication of Janssen vaccine (first dose and the lot number was 1805022) on 15-Mar-2021 and Flu vaccine on 01-Nov-2021. Past adverse reactions to the above products included No adverse event with Flu vaccine and Janssen vaccine. On 01-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED. On 01-Nov-2021, EXPIRED PRODUCT ADMINISTERED had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant medications were reported. No Treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- -
- Geschlecht
- U
- Eingang
- 13.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received vaccine after expiry date; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after expiry date) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after expiry date). On 29-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after expiry date) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. It was reported that Patient received 1st Janssen dose on 12 May 2021, lot number was 205A21A. Concomitant product use was not provided by the reporter. Treatment information was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 13.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine after expiry date) in a 30-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. Previously administered products included for COVID-19 vaccination: PFIZER BIONTECH COVID-19 VACCINE (2nd dose of Pfizer vaccine.) on 30-Mar-2021 and PFIZER BIONTECH COVID-19 VACCINE (1st dose of Pfizer vaccine). On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED. On 29-Oct-2021, EXPIRED PRODUCT ADMINISTERED had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications details were not reported by the reporter. Treatment details was not reported by the reporter. Pharmacist was unaware if patient was taking medication. Pharmacist was unaware if patient had the side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
This spontaneous case reported by a pharmacist, describes the occurrence of administered expired product (patient received vaccine after expiry date) in a 28-year-old female patient who received mRNA-1273 (Moderna COVID-19 vaccine, batch/lot# 049E21A) for COVID-19 immunization. No medical history reported. On Oct 29, 2021, patient received the third dose of mRNA-1273 (Moderna COVID-19 vaccine), intramuscular; 1 dosage form. On Oct 29, 2021, patient administered expired product (patient received vaccine after expiry date). On Oct 29, 2021, administered expired product (patient received vaccine after expiry date) resolved. The reporter did not provide any causality assessments, concomitant medication or treatment information. Patient received first dose of Pfizer vaccine on an unspecified date; second dose of Pfizer vaccine on Mar 31, 2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 09.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine given; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine given) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine given). On 29-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine given) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medication was reported. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 04-Nov-2021: follow-up document contains no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.11.2021
- Impfdatum
- 09.09.2021
- Beginn
- 09.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patients received expired vaccine; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients received expired vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Sep-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients received expired vaccine). On 09-Sep-2021, EXPIRED PRODUCT ADMINISTERED (Patients received expired vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments.Concomitant medication information was not provided by the reporter.Treatment information was not provided by the reporter. Two vials where used 14 patients received the vaccine on 19OCT2021 and 8 patients on received the vaccine on 22OCT2021.expiration date the vaccine was on 12OCT2021. This case was linked to MOD-2021-363630 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 22-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 22-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication was provided by the reporter. No treatment information was provided. Patient took vaccine on Deltoid. This case was linked to MOD-2021-361706 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine used) in a 21-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 19-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine used). On 19-Oct-2021, EXPIRED PRODUCT ADMINISTERED (expired vaccine used) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. Treatment information was not provided by the reporter. Patient received vaccine in deltoid. This case was linked to MOD-2021-361706 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine used) in an 85-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 19-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine used). On 19-Oct-2021, EXPIRED PRODUCT ADMINISTERED (expired vaccine used) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired dose was given to a patient; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose was given to a patient) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose was given to a patient). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose was given to a patient) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. Treatment information was not provided by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 02-Nov-2021: Follow-up was received on 2-NOV-2021 and contains no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 06.11.2021
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine used) in a 61-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 21-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 ml. On 21-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine used). On 21-Oct-2021, EXPIRED PRODUCT ADMINISTERED (expired vaccine used) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. Treatment information was not provided by the reporter. This case was linked to MOD-2021-361706 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine used) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 ml. On 19-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine used). On 19-Oct-2021, EXPIRED PRODUCT ADMINISTERED (expired vaccine used) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant medications was provided by the reporter. No Treatment medications was provided by the reporter. This case was linked to MOD-2021-361706 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 18-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). On 18-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications was provided by the reporter. No treatment was provided by the reporter. Vaccine was administered on Deltoid. This case was linked to MOD-2021-361706 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine used) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 22-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine used). On 22-Oct-2021, EXPIRED PRODUCT ADMINISTERED (expired vaccine used) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication were reported. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
An expired 2nd dose was given to a patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (An expired 2nd dose was given to a patient) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 ml. On 14-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (An expired 2nd dose was given to a patient). On 14-Oct-2021, EXPIRED PRODUCT ADMINISTERED (An expired 2nd dose was given to a patient) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment medications were provided. The vial didn't undergo any temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
An expired booster was given to a patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (An expired booster was given to a patient) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (An expired booster was given to a patient). On 25-Oct-2021, EXPIRED PRODUCT ADMINISTERED (An expired booster was given to a patient) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided by reporter. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- M
- Eingang
- 06.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
An expired booster dose was given to a patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient). On 25-Oct-2021, EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant treatment was provided. No medical information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
An expired 2nd dose was given to a patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (An expired 2nd dose was given to a patient) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (An expired 2nd dose was given to a patient). On 14-Oct-2021, EXPIRED PRODUCT ADMINISTERED (An expired 2nd dose was given to a patient) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was mentioned. No treatment medication was mentioned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- M
- Eingang
- 06.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
An expired booster dose was given to a patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient). On 25-Oct-2021, EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications was reported. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- M
- Eingang
- 06.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
An expired booster dose was given to a patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient). On 28-Oct-2021, EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
An expired booster dose was given to a patient; This spontaneous case was reported by a health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient). On 28-Oct-2021, EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product use was provided by the reporter. No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- 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: ja
Expired product administered
Symptomtext
Expired vaccine adminstered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CAD
- Andere Medikamente
- Atorvastatin, Lisinopril, Clopidogrel, Metoprolol
- Allergien
- Latex, natural rubber
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- 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: ja
Product storage error
Symptomtext
Expired vaccine administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, RA
- Andere Medikamente
- Levothyroxine, Albuterol, Spironolactone, Amiodarone, Ergocalciferol, Potassium Chloride, Metoprolol
- Allergien
- Iodine, NSAIDS, Iohexol
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- 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: ja
Product storage error
Symptomtext
Expired vaccine administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Iodine
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 05.11.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Expired vaccine administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 05.11.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Extra dose administered
Symptomtext
Expired vaccine administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Levetiracetam
- Allergien
- Latex, natural rubber
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Coconut, seafood
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 19.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired vaccine used; This spontaneous case was reported by a health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired vaccine used) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired vaccine used). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired vaccine used) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
An expired booster dose was given to a patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient). On 28-Oct-2021, EXPIRED PRODUCT ADMINISTERED (An expired booster dose was given to a patient) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided by reporter. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 05.11.2021
- Impfdatum
- 23.10.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
330 patients Received expired dose of the vaccine; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (330 patients Received expired dose of the vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (330 patients Received expired dose of the vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (330 patients Received expired dose of the vaccine) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications was not provided by the reporter. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 12.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was administered a dose from an expired vial.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.). On 12-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medication was not provided. Treatment information was not provided. This case was linked to MOD-2021-366918, MOD-2021-366925 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 04.11.2021
- Impfdatum
- 15.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was administered a dose from an expired vial; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial) in a 43-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial). On 15-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were provided. No treatment information was provided. Expiration date was 11 Oct 2021. This case was linked to MOD-2021-366918, MOD-2021-365543, MOD-2021-365600, MOD-2021-365692, MOD-2021-365742, MOD-2021-365891, MOD-2021-366043, MOD-2021-366226, MOD-2021-366595 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 13.10.2021
- Beginn
- 13.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was administered a dose from an expired vial.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.). On 13-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported No treatment medications were reported. This case was linked to MOD-2021-366918, MOD-2021-366925 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 12.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was administered a dose from an expired vial.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.). On 12-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications reported. No treatment reported This case was linked to MOD-2021-366918 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 04.11.2021
- Impfdatum
- -
- Beginn
- 14.10.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was administered a dose from an expired vial; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial) in a 31-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial). On 14-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant and Treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was administered a dose from an expired vial.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.). On 22-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment medications are provided by the reporter. Patient reported that there was a transcription error when taking notes of the expiration dates of the lot for the vials they have at their facility. They've mistakenly administered expired vials to 10 patients. This case was linked to MOD-2021-366918, MOD-2021-366925 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 04.11.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was administered a dose from an expired vial.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) in a 25-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.). On 18-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided. Treatment information was not provided. This case was linked to MOD-2021-366918 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 04.11.2021
- Impfdatum
- 15.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was administered a dose from an expired vial; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial) in a 57-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial). On 15-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment information was provided. This case was linked to MOD-2021-366918, MOD-2021-365600, MOD-2021-365692, MOD-2021-365742, MOD-2021-365891, MOD-2021-366043, MOD-2021-366226, MOD-2021-366595, MOD-2021-366925 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 04.11.2021
- Impfdatum
- 15.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was administered a dose from an expired vial. This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) in a 42-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.). On 15-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were provided. No treatment information was provided. Expiration date of vial was 11 Oct 2021. This case was linked to MOD-2021-365891, MOD-2021-366043, MOD-2021-366595, MOD-2021-365742, MOD-2021-365543, MOD-2021-366925, MOD-2021-366226, MOD-2021-365600, MOD-2021-365692 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was administered a dose from an expired vial.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) in a 28-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.). On 18-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose from an expired vial.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment medication was provided. This case was linked to MOD-2021-366918, MOD-2021-366925 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
received an expired dose as a booster dose; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received an expired dose as a booster dose) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 26-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 26-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (received an expired dose as a booster dose). On 26-Oct-2021, EXPIRED PRODUCT ADMINISTERED (received an expired dose as a booster dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not reported. This case was linked to MOD-2021-365005 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
received an expired dose as a booster dose; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received an expired dose as a booster dose) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 26-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 26-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (received an expired dose as a booster dose). On 26-Oct-2021, EXPIRED PRODUCT ADMINISTERED (received an expired dose as a booster dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment medications were reported. Date the vial was initially stored in the refrigerator: 26-Oct-2021. The vial did not undergo any temperature excursions. This case was linked to MOD-2021-365107 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Received booster dose from expired vial; This spontaneous case was reported by a consumer and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received booster dose from expired vial) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received booster dose from expired vial). On 22-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Received booster dose from expired vial) had resolved. Concomitant product use was not provided by the reporter. Treatment information was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired vaccine was expired to 13 patients./Expired vaccine was expired to 9 patients.; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine was expired to 13 patients./Expired vaccine was expired to 9 patients.) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 26-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine was expired to 13 patients./Expired vaccine was expired to 9 patients.). On 26-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Expired vaccine was expired to 13 patients./Expired vaccine was expired to 9 patients.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant medications were provided No treatment medications were provided. Most recent FOLLOW-UP information incorporated above includes: On 26-Oct-2021: Significant Follow up; start date for vaccination given
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/30/21. Vial expired 10/11/21. Vial was kept in freezer until 10/29/2021 and removed to fridge on 10/29/2021 for administration on 10/30/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 11/01/21. Vial expired 10/11/21. Vial was kept in freezer until 10/30/2021 and removed to fridge on 10/30/2021 for administration on 11/01/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/30/21. Vial expired 10/11/21. Vial was kept in freezer until 10/29/2021 and removed to fridge on 10/29/2021 for administration on 10/30/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/30/21. Vial expired 10/11/21. Vial was kept in freezer until 10/29/2021 and removed to fridge on 10/29/2021 for administration on 10/30/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Maternal exposure before pregnancy
Symptomtext
Booster dose. Vaccine administered on 11/1/2021. Vial expired 10/11/21. Vial was kept in freezer until 10/30/2021 and removed to fridge on 10/30/2021 for administration on 11/01/2021. Regarding potential for pregnancy, pt answered yes to this question: Are you pregnant or is there a chance you could become pregnant during the next month? Patient answered YES to this question. Given that this vaccine is still recommended during pregnancy, no additional information was gleaned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Extra dose administered
Product storage error
Symptomtext
Booster dose. Vaccine administered on. Vial expired 10/11/21. Vial was removed from freezer to fridge on 10/30/2021 for administration on 11/1/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 30.10.2021
- 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
SECOND DOSE Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Booster dose. Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine administered on 10/29/21. Vial expired 10/11/21. Vial was kept in freezer until 10/28/2021 and removed to fridge on 10/28/2021 for administration on 10/29/2021. No adverse effects reported from patient to date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
EXPIRED LOT WAS GIVEN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Received dose from expired vial; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received dose from expired vial) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received dose from expired vial). In October 2021, EXPIRED PRODUCT ADMINISTERED (Received dose from expired vial) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient received booster dose of vaccine on 23 Oct 2021 and 24 Oct 2021. No concomitant medication was reported. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patients received expired vaccine; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients received expired vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients received expired vaccine). In October 2021, EXPIRED PRODUCT ADMINISTERED (Patients received expired vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment information was reported. Two vials where used 14 patients received the vaccine on 19-OCT-2021 and 8 patients received the vaccine on 22-OCT-2021,However the expiration date the vaccine expired on was 12-OCT-2021. She stated she had 112 doses ready to be dispose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired Moderna COVID19 Vaccine/ Inadvertently used a lot that looks like it had expired; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Moderna COVID19 Vaccine/ Inadvertently used a lot that looks like it had expired) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Moderna COVID19 Vaccine/ Inadvertently used a lot that looks like it had expired). In October 2021, EXPIRED PRODUCT ADMINISTERED (Expired Moderna COVID19 Vaccine/ Inadvertently used a lot that looks like it had expired) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment medications were reported. The pharmacist stated that 3 doses of the expired Moderna COVID19 Vaccine were given on 23-Oct-2021 and 3 doses on 24-Oct-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.11.2021
- Impfdatum
- 20.10.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient got a dose of an expired vaccine; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient got a dose of an expired vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient got a dose of an expired vaccine). On 20-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Patient got a dose of an expired vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that the vial was initially stored in the refrigerator 1 or 2 days before 20-Oct-2021 and the vial did not undergone any temperature excursions. The vial was expired on 11-Oct-2021. No concomitant medications were reported No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 26-Oct-2021: Non Significant follow-up received reporter fax number added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
patient who had been administered the Moderna covid-19 vaccine today who afterwards looked up the expiration date using the online tool showing an expiration date of 11OCT2021; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient who had been administered the Moderna covid-19 vaccine today who afterwards looked up the expiration date using the online tool showing an expiration date of 11OCT2021) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient who had been administered the Moderna covid-19 vaccine today who afterwards looked up the expiration date using the online tool showing an expiration date of 11OCT2021). On 22-Oct-2021, EXPIRED PRODUCT ADMINISTERED (patient who had been administered the Moderna covid-19 vaccine today who afterwards looked up the expiration date using the online tool showing an expiration date of 11OCT2021) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Treatment medications were provided No Concomitant medications were provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine was expired when given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 17.10.2021
- Beginn
- 17.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Pharmacist called in to report patients received an expired dose of the Moderna vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Pharmacist called in to report patients received an expired dose of the Moderna vaccine) in a 57-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Pharmacist called in to report patients received an expired dose of the Moderna vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Pharmacist called in to report patients received an expired dose of the Moderna vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 17.10.2021
- Beginn
- 17.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
administered an expired dose; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered an expired dose) in a 41-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered an expired dose). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered an expired dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Dose administered after manufacturer date of expiry[11October2021Number of doses/vials:1 vial, 4 doses for 4 patients Date the vial was initially stored in the refrigerator: 17October2021 Date(s) of administration of vaccine: 17October2021 No concomitant medications were reported No treatment information was provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 17.10.2021
- Beginn
- 17.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Administration of an expired dose; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administration of an expired dose) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administration of an expired dose). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administration of an expired dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment information were reported by the reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 17.10.2021
- Beginn
- 17.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
administered an expired dose; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered an expired dose) in a 26-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered an expired dose). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered an expired dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment information were reported by the reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Extra dose administered
Symptomtext
MODERNA BOOSTER ADMINISTERED PAST THE EXPIRATION DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HODGKIN'S LYMPHOMA IN REMISSION STAGE 3 -MULT SITES W INTRATHORACIC, INTRA-ABDOMINAL LYMPH NODES - ADENOPATHY MIXED LIPIDS DM II W NEUROPATHY / POLYNEUROPATHY DM II W HYPERTRIGLYCERIDEMIA DM II W/ CKD 3A DM II WITH OTHER DIABETIC ARTHROPATHY RELATED TO MILD BUNIONS AND TOE DEFORMITIES DM II W DIABETIC PERIPHERAL ANGIOPATHY WO GANGRENE DM II W ONYCHOMYCOSIS DM II W/ OTHER CIRCULATORY COMPLICATIONS RELATED TO CAD Type 2 diabetes mellitus with periodontal disease DM II WITH OTHER DIABETIC OPHTHALMIC COMPLICATION RELATED TO GLAUCOMA ATHEROSCLEROTIC HEART DISEASE OF NATIVE CORONARY ARTERY WO ANGINA PECTORIS CAD - LEXISCAN W INF WALL ISCHEMIA ATHEROSCLEROSIS OF NATIVE ARTERY OF BOTH LOWER EXTREMITIES HYPERTENSIVE HEART AND RENAL DISEASE / CKD3 A2 WITH CHRONIC DIASTOLIC CHF EF 60-65% GERD S/P CHOLECYSTECTOMY S/P CATARACT SURGERY VIT B 12 DEFICIENCY ANEMIA VENOUS INSUFFICIENCY OF BOTH LOWER EXTREMITIES OSTEOPOROSIS VIT D DEFICIENCY / OSTEOMALACIA OPEN ANGLE GLAUCOMA SUSPECT MACULAR PUCKERING HX COLON POLYPS, INTERNAL AND EXTERNAL HEMORRHOIDS IMMUNODEFICIENCY DUE TO CONDITIONS CLASSIFIED ELSEWHERE RELATED TO CIRRHOSIS CIRRHOSIS - MELD SCORE 12 WITH CHRONIC HEPATITIS HYPERSPLENISM WITH PORTAL HYPERTENSION SECONDARY HYPERALDOSTERONISM THROMBOCYTOPENIA - CHRONIC - DUE TO CHEMO/DRUG STOMACH METAPLASIA AFIB- CHRONIC WITH SECONDARY HYPERCOAGULABLE STATE DUE TO AFIB LONG TERM ANTICOAGULATION ON ELIQUIS CHRONIC DIASTOLIC CHF EF55 % LAD AND LVH OBESE / BMI 31 STATIN INDUCED MYALGIAS GASTRIC METAPLASIA PORTAL HYPERTENSION DUE TO CIRRHOSIS SENILE PURPURA
- Andere Medikamente
- docusate sodium 100 mg capsule: 1 capsule 2 times a day Eliquis 5 mg tablet: 1 tablet 2 times a day for 90 days, Simbrinza 1 %-0.2 % eye drops,suspension: 1 drop bid to both eyes potassium chloride ER 20 mEq tablet,extended release: 1 tabl
- Allergien
- ASPIRIN LOVASTATIN PRAVASTATIN
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
BOOSTER VACCINE ADMINISTRATION PAST THE EXPIRATION DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HYPOTHYROIDISM GERD ALLERGIC RHINITIS DOWN'S SYNDROME FATTY LIVER GALL STONES ACNE ROSACEA RESTLESS LEG SYN CHOLESTEATOMA - RIGHT EAR - TYMPANOMASTOIDECTOMY BMI 27 ECZEMA VASAL VAGAL SYNCOPE
- Andere Medikamente
- FAMOTIDINE 20MG QD PRN LEVOTHYROXINE 112MCG DAILY EXCEPT 0.5TABLET SUNDAY LORATADINE 10MG DAILY PRN MIRALAX 17GM DAIY PRN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna COVID?19 Vaccine EUA ADMINISTERED PAST THE EXPIRATION DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ASPIRIN 81MG DAILY CALCITROL 0.25MCG 3CAPS DAILY CETIRIZINE 10MG DAILY FAMOTIDINE 20MG DAILY PRN HYDROCHLOROTHIAZIDE 25MG DAILY IBUPROFEN 600MG QHS PRN LEVOTHYROXINE 175MCG 1 TABLET DAILY EXCEPT 0.5TAB SATURDAY & SUNDAY LEXAPRO 10MG QHS VI
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna COVID?19 Vaccine EUA ADMINISTERED PAST THE EXPIRATION DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Moderna COVID?19 Vaccine EUA ADMINISTERED PAST EXPIRATION DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ASPIRIN 81MG DAILY METOPROLOL TARTRATE 12.5MG BID TOPAMAX 50MG DAILY CARBAMEZAPINE 200MG 0.5 TABLET BID LOVASTATIN 40MG QHS
- Allergien
- MORPHINE PPD SKIN TEST
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Balance issues
- Vorgeschichte
- Parkinson's disease arthropathy rheumatoid arthritis factor myalgia/myositis - multiple impairment of balance physical therapist referral
- Andere Medikamente
- carbidopa-levodopa clonazepam prednisone rasagiline Rytary sertraline Xadago
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Moderna COVID-19 booster dose (0.25mL) administered on Oct 26, 2021 before checking expiration date of Oct 11, 2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acute upper respiratory infection; anemia; herpes labialis; hyperlipidemia (screening); injury of lower leg (right); insomnia; malaise; fatigue; mixed urinary incontinence
- Andere Medikamente
- Acetaminophen/Codeine; Denavir; Drysol; Permethrin; Polymyxin-B Sulf-Trimethoprim; Progesterone micronized; Valtrex (valacyclovir); Zolpidem
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 26.10.2021
- 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: ja
Wrong product administered
Symptomtext
Wrong vaccine given to patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Iron Deficiency Anemia, Anxiety
- Andere Medikamente
- Multivitamin, Sertraline, Iron
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
administered with an expired vaccine; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with an expired vaccine) in a 29-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 ml. On 18-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with an expired vaccine). On 18-Oct-2021, EXPIRED PRODUCT ADMINISTERED (administered with an expired vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication details was reported. No treatment medication details was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 23.10.2021
- Impfdatum
- 01.09.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 30,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abscess limb
Culture wound
Laboratory test
Localised infection
Surgery
Symptomtext
Shortly after my initial 1st dose I ended up with a serious infection and abscess in my right arm need almost 2 weeks of iv antibiotic therapy as well as surgical intervention. Never in my life have I had issues with medication however this even I did not respond to any oral antibiotics causing my infection to worsen. My doctor said this may be a result of the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abscess limb
- Hospital-Tage
- 11,0
- Labordaten
- Wound cultures (10/4/21) Lab work (10/4 through 10/19) almost daily.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Vancomycin, Penicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 22.10.2021
- Impfdatum
- 24.09.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Peripheral swelling
Symptomtext
Left leg swelling 1 week after 1st moderna vaccination Swelling decreased over time. No swelling by the time pt arrived for the second dose in the moderna vaccination series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Peripheral swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 21.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Given a vaccine that expired yesterday; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Given a vaccine that expired yesterday) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Given a vaccine that expired yesterday). On 12-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Given a vaccine that expired yesterday) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant product was provided. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 19.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Pt was given expired vaccine. Lot # 049e21a Moderna exp 10-11-21. Vaccine was administered on 10-18-21. As of the morning of 10-19-21 no adverse effects had been reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 18.10.2021
- Impfdatum
- 13.10.2021
- Beginn
- 13.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
NONE VIAL SENT WITH WRONG EXPIRATION DATE ON BAG NO DATE ON VIAL ITSELF
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 18.10.2021
- Impfdatum
- 13.10.2021
- Beginn
- 13.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
none . Vial sent with wrong Expiration date . expired 2 days after vaccine was administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Poor quality product administered
Product storage error
Symptomtext
vaccine that had experienced a temperature excursion was given as 1st dose; poor quality product administered; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT STORAGE ERROR (vaccine that had experienced a temperature excursion was given as 1st dose) and POOR QUALITY PRODUCT ADMINISTERED (poor quality product administered) in a 33-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Sep-2021, the patient experienced PRODUCT STORAGE ERROR (vaccine that had experienced a temperature excursion was given as 1st dose) and POOR QUALITY PRODUCT ADMINISTERED (poor quality product administered). At the time of the report, PRODUCT STORAGE ERROR (vaccine that had experienced a temperature excursion was given as 1st dose) and POOR QUALITY PRODUCT ADMINISTERED (poor quality product administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment medication was provided. The refrigerator was cooled a little bit more than normal. Six vials stored in the refrigerator were exposed to temperatures below 36?F. Minimum temperature was 34.7?F. There were 145 incidents in total and each one lasted less than 15 minutes: 142 times fridge temperatures were between 35?F and 36?F; while three times temperatures were under 35?F, reaching 34.7?F (minimum). Five patients received doses from four of the 6 vials.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 28.09.2021
- Beginn
- 28.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
vaccine that had experienced a temperature excursion was given as 1st dose; vaccine that had experienced a temperature excursion was given as 1st dose; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT STORAGE ERROR (vaccine that had experienced a temperature excursion was given as 1st dose) and EXPIRED PRODUCT ADMINISTERED (vaccine that had experienced a temperature excursion was given as 1st dose) in a 22-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Sep-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Sep-2021, the patient experienced PRODUCT STORAGE ERROR (vaccine that had experienced a temperature excursion was given as 1st dose). On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine that had experienced a temperature excursion was given as 1st dose). At the time of the report, PRODUCT STORAGE ERROR (vaccine that had experienced a temperature excursion was given as 1st dose) and EXPIRED PRODUCT ADMINISTERED (vaccine that had experienced a temperature excursion was given as 1st dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Accidental overdose
Symptomtext
administered 1 ml of the Moderna COVID-19 vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL OVERDOSE (administered 1 ml of the Moderna COVID-19 vaccine) in a 29-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced ACCIDENTAL OVERDOSE (administered 1 ml of the Moderna COVID-19 vaccine). At the time of the report, ACCIDENTAL OVERDOSE (administered 1 ml of the Moderna COVID-19 vaccine) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product was not provided by the reporter Treatment information was not provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental overdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 14.10.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine given 3 days past vial expiration date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 14.10.2021
- Impfdatum
- 13.10.2021
- Beginn
- 13.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
PT WAS ADMINISTERED EXPIRED VACCINE. MODERNA EXPIRED ON 10/11/21. IT WAS ADMINISTERED ON 10/13/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- IMMUNOSUPPRESSED
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE REPORTED
- Vorherige Impfungen
- -
- Staat
- GU
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 12.10.2021
- Impfdatum
- 09.10.2021
- Beginn
- 11.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Epistaxis
Intermenstrual bleeding
Lymphadenopathy
Symptomtext
NOSEBLEED -- HEAVY FOR 20 MINUTES SPOTTING LYMPH NODE SWELLING
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Epistaxis
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- DMII ASTHMA -- ONLY AS A CHILD
- Andere Medikamente
- CENTRUM CHOLESTOFF NATURE MADE JARDIANCE TRULICITY TYLENOL
- Allergien
- COLD WEATHER -- GETS HIVES METFORMIN -- DIARRHEA
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 09.10.2021
- Impfdatum
- 23.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vaccine that had experienced a temperature excursion was given as 2nd dose; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT STORAGE ERROR (Vaccine that had experienced a temperature excursion was given as 2nd dose) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Sep-2021, the patient experienced PRODUCT STORAGE ERROR (Vaccine that had experienced a temperature excursion was given as 2nd dose). On 23-Sep-2021, PRODUCT STORAGE ERROR (Vaccine that had experienced a temperature excursion was given as 2nd dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 09.10.2021
- Impfdatum
- 23.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Six (6) vials stored in the refrigerator were exposed to temperatures below 36?F; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT STORAGE ERROR (Six (6) vials stored in the refrigerator were exposed to temperatures below 36?F) in a 66-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Sep-2021, the patient experienced PRODUCT STORAGE ERROR (Six (6) vials stored in the refrigerator were exposed to temperatures below 36?F). On 23-Sep-2021, PRODUCT STORAGE ERROR (Six (6) vials stored in the refrigerator were exposed to temperatures below 36?F) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant medications were reported. Reporter called to check on a temperature excursion. Refrigerator was cooling a little bit more than normal. Six (6) vials stored in the refrigerator were exposed to temperatures below 36?F. Minimum temperature was 34.7?F. There were 145 incidents in total and each one lasted less than 15 minutes: 142 times fridge temperatures were between 35?F and 36?F; while 3 times temperatures were under 35?F, reaching 34.7?F (minimum). Patient had experienced a temperature excursion. No Treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 08.10.2021
- Impfdatum
- 08.10.2021
- Beginn
- 08.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
Symptomtext
patient stated he had not been vaccinated until he received the dose of moderna on 10/08/21, already received 1st dose of pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 08.10.2021
- Impfdatum
- 01.09.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 35,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exposure during pregnancy
Foetal heart rate abnormal
Ultrasound antenatal screen abnormal
Symptomtext
At 8 weeks gestation baby had a heartbeat and was healthy. Got the vaccine two days later. Next sonogram visit at 9.5 weeks, no heartbeat detected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure during pregnancy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Prenatal vitamins
- Allergien
- Keflex
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 08.10.2021
- Impfdatum
- 23.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
Vials stored in the refrigerator were exposed to temperatures below 36?F; vaccine that had experienced a temperature excursion was given as 2nd dose; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT STORAGE ERROR (Vials stored in the refrigerator were exposed to temperatures below 36?F) and EXPIRED PRODUCT ADMINISTERED (vaccine that had experienced a temperature excursion was given as 2nd dose) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Sep-2021, the patient experienced PRODUCT STORAGE ERROR (Vials stored in the refrigerator were exposed to temperatures below 36?F) and EXPIRED PRODUCT ADMINISTERED (vaccine that had experienced a temperature excursion was given as 2nd dose). On 23-Sep-2021, PRODUCT STORAGE ERROR (Vials stored in the refrigerator were exposed to temperatures below 36?F) and EXPIRED PRODUCT ADMINISTERED (vaccine that had experienced a temperature excursion was given as 2nd dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant medications were provided. No Treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 18.08.2021
- Beginn
- 25.08.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vision blurred
Symptomtext
significant blurred vision
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vision blurred
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- coryza vitd,c,b zinc
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 25.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Menstruation irregular
Symptomtext
Menstrual period delayed by approximately 2 weeks; This spontaneous case was reported by a consumer and describes the occurrence of MENSTRUATION IRREGULAR (Menstrual period delayed by approximately 2 weeks) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 049E21A and 004F21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 22-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to .5 milliliter. In September 2021, the patient experienced MENSTRUATION IRREGULAR (Menstrual period delayed by approximately 2 weeks). At the time of the report, MENSTRUATION IRREGULAR (Menstrual period delayed by approximately 2 weeks) outcome was unknown. Concomitant medication was not provided. The patient was expecting menstrual period on 23-Aug-2021 but it came 1st week of September approximately 2 weeks delayed). Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstruation irregular
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 05.10.2021
- Impfdatum
- 18.09.2021
- Beginn
- 18.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product dose omission issue
Symptomtext
RPH gave patient without medication and noticed right away and gave patient vacination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product dose omission issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NA
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 03.10.2021
- Beginn
- 03.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
PATIENT REQUESTED A MODERNA 3RD DOSE SINCE SHE IS immunocompromised , after administering the moderna vaccine she returned and stated she was suppose to ask for pfizer vaccine since she remembered her first 2 doses were pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 30.09.2021
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immunodeficiency
Interchange of vaccine products
Symptomtext
Patient's wife brought him to get third shot because she feels he is immunocompromised due to his age. They were informed patient was getting a Moderna shot and patient/wife signed the waiver. After he was given the shot, the nurse was given the COVID vaccine card and saw his previous two shots were Pfizer shots. The couple was told he has now received a Moderna shot and to notify the office if he does poorly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunodeficiency
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- BPH, Diverticulosis, HTN, Hyperlipidemia
- Vorgeschichte
- See above
- Andere Medikamente
- Amlodipine Besylate, Fluocinonide, levetiracetam, Tamsulosin, allopurinol
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 28.09.2021
- Beginn
- 28.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Patient thought she was getting her third dose of the vaccine, presented to our office without her covid vaccination card, when asked if she was immunicompromised, said yes and she wanted the Moderna shot. We gave her the shot. In inputting the information into the system, we realized her first two shots were Pfizer shots.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- diabetes, htn, hyperlipidemia, arthralgias, constipation
- Vorgeschichte
- see above
- Andere Medikamente
- Eliquis, Cordorane, levothyroxine, montelukast, Norco
- Allergien
- amoxicillin, sulfa, nubain, prednisone
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 28.09.2021
- Impfdatum
- 14.08.2021
- Beginn
- 18.09.2021
- Tage bis Beginn
- 35,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Disturbance in attention
Feeling hot
Visual impairment
Symptomtext
changed her vision; having trouble focusing; doesn't have a temperature but she feels hot; This spontaneous case was reported by a consumer and describes the occurrence of VISUAL IMPAIRMENT (changed her vision), DISTURBANCE IN ATTENTION (having trouble focusing) and FEELING HOT (doesn't have a temperature but she feels hot) in a 26-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 037F21A and 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 18-Sep-2021, the patient experienced VISUAL IMPAIRMENT (changed her vision), DISTURBANCE IN ATTENTION (having trouble focusing) and FEELING HOT (doesn't have a temperature but she feels hot). At the time of the report, VISUAL IMPAIRMENT (changed her vision), DISTURBANCE IN ATTENTION (having trouble focusing) and FEELING HOT (doesn't have a temperature but she feels hot) outcome was unknown. It was reported that patient had anxiety, but no Concomitant drug details provided for anxiety. Treatment details were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Disturbance in attention
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 07.09.2021
- Beginn
- 18.09.2021
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Musculoskeletal stiffness
Symptomtext
Stiffness in right arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal stiffness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- diabetic asthma
- Andere Medikamente
- abilify 10mg iron 325 mg
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 18.09.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
No adverse event
Symptomtext
No adverse reaction. Patient received complete moderna series after getting Jannsen from another provider.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 17.09.2021
- Impfdatum
- 18.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- -
- 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 event(s) to report. Vaccine was given to a a 17 year old due to incorrect calculation of age by staff.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 08.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Heavy menstrual bleeding
Intentional dose omission
Uterine haemorrhage
Symptomtext
After first shot patient had uterine bleeding felt like super heavy period about 3 to 7 days after Moderna vaccine; Felt like super heavy period about 3 to 7 days after Moderna vaccine/ The bleeding episode happened anywhere from three to seven days after the first dose; Intentional Dose omission; This spontaneous case was reported by a pharmacist and describes the occurrence of UTERINE HAEMORRHAGE (After first shot patient had uterine bleeding felt like super heavy period about 3 to 7 days after Moderna vaccine), HEAVY MENSTRUAL BLEEDING (Felt like super heavy period about 3 to 7 days after Moderna vaccine/ The bleeding episode happened anywhere from three to seven days after the first dose) and INTENTIONAL DOSE OMISSION (Intentional Dose omission) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. The patient's past medical history included Uterine abrasion (Patient has a history of uterine abrasions). On 08-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced UTERINE HAEMORRHAGE (After first shot patient had uterine bleeding felt like super heavy period about 3 to 7 days after Moderna vaccine), HEAVY MENSTRUAL BLEEDING (Felt like super heavy period about 3 to 7 days after Moderna vaccine/ The bleeding episode happened anywhere from three to seven days after the first dose) and INTENTIONAL DOSE OMISSION (Intentional Dose omission). At the time of the report, UTERINE HAEMORRHAGE (After first shot patient had uterine bleeding felt like super heavy period about 3 to 7 days after Moderna vaccine) and HEAVY MENSTRUAL BLEEDING (Felt like super heavy period about 3 to 7 days after Moderna vaccine/ The bleeding episode happened anywhere from three to seven days after the last dose) outcome was unknown and INTENTIONAL DOSE OMISSION (Intentional Dose omission) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment information was provided.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. Patient?s history of uterine abrasions is a confounder for the event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heavy menstrual bleeding
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Uterine abrasion (Patient has a history of uterine abrasions)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Overdose
Symptomtext
Administered 1 ml of the Moderna COVID-19 vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of OVERDOSE (Administered 1 ml of the Moderna COVID-19 vaccine) in a 26-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 milliliter. On an unknown date, the patient experienced OVERDOSE (Administered 1 ml of the Moderna COVID-19 vaccine). At the time of the report, OVERDOSE (Administered 1 ml of the Moderna COVID-19 vaccine) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Pharmacist didn't mentioned any side effect. No concomitant product information was provided. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Overdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Accidental overdose
Symptomtext
administered 1 ml of the Moderna COVID-19 vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL OVERDOSE (administered 1 ml of the Moderna COVID-19 vaccine) in a 28-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 milliliter. On an unknown date, the patient experienced ACCIDENTAL OVERDOSE (administered 1 ml of the Moderna COVID-19 vaccine). At the time of the report, ACCIDENTAL OVERDOSE (administered 1 ml of the Moderna COVID-19 vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications was not reported. Treatment medications was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental overdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 17.09.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Administered 1 ml of the Moderna COVID-19 vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXTRA DOSE ADMINISTERED (Administered 1 ml of the Moderna COVID-19 vaccine) in a 29-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXTRA DOSE ADMINISTERED (Administered 1 ml of the Moderna COVID-19 vaccine). At the time of the report, EXTRA DOSE ADMINISTERED (Administered 1 ml of the Moderna COVID-19 vaccine) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications reported. No treatment information was reported by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- -
- Geschlecht
- F
- Eingang
- 13.09.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Overdose
Symptomtext
administered 1 ml of the Moderna COVID-19 vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of OVERDOSE (administered 1 ml of the Moderna COVID-19 vaccine) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 ml. On an unknown date, the patient experienced OVERDOSE (administered 1 ml of the Moderna COVID-19 vaccine). At the time of the report, OVERDOSE (administered 1 ml of the Moderna COVID-19 vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant drugs were reported. No Treatment information were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Overdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 13.09.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Overdose
Symptomtext
administered 1 ml of the Moderna COVID-19 vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of OVERDOSE (administered 1 ml of the Moderna COVID-19 vaccine) in a 26-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 milliliter. On an unknown date, the patient experienced OVERDOSE (administered 1 ml of the Moderna COVID-19 vaccine). At the time of the report, OVERDOSE (administered 1 ml of the Moderna COVID-19 vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. Treatment information was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Overdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 11.09.2021
- Impfdatum
- 01.09.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Maternal exposure during pregnancy
Symptomtext
received 1st dose while pregnant; This spontaneous prospective pregnancy case was reported by a consumer and describes the occurrence of MATERNAL EXPOSURE DURING PREGNANCY (received 1st dose while pregnant) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 01-Sep-2021, the patient experienced MATERNAL EXPOSURE DURING PREGNANCY (received 1st dose while pregnant). On 01-Sep-2021, MATERNAL EXPOSURE DURING PREGNANCY (received 1st dose while pregnant) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No relevant concomitant medications were reported. Treatment medication was not provided by the reporter.; Sender's Comments: This is a case of maternal exposure during pregnancy of a 27 year old Female with no associated AEs. Patient will continue to be contacted for further monitoring.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Maternal exposure during pregnancy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 11.09.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Loss of libido
Symptomtext
loss of sexual desire; This spontaneous case was reported by a consumer and describes the occurrence of LOSS OF LIBIDO (loss of sexual desire) in a 36-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Aug-2021, the patient experienced LOSS OF LIBIDO (loss of sexual desire). At the time of the report, LOSS OF LIBIDO (loss of sexual desire) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medication was not provided Treatment information was not reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of libido
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 11.09.2021
- Impfdatum
- 17.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site erythema
Vaccination site induration
Symptomtext
hard red spot on the deltoid near the injection site about the size of a half dollar; hard red spot on the deltoid near the injection site about the size of a half dollar; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE INDURATION (hard red spot on the deltoid near the injection site about the size of a half dollar) and VACCINATION SITE ERYTHEMA (hard red spot on the deltoid near the injection site about the size of a half dollar) in a 32-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. Concomitant products included VITAMINS NOS for an unknown indication. On 17-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VACCINATION SITE INDURATION (hard red spot on the deltoid near the injection site about the size of a half dollar) and VACCINATION SITE ERYTHEMA (hard red spot on the deltoid near the injection site about the size of a half dollar). At the time of the report, VACCINATION SITE INDURATION (hard red spot on the deltoid near the injection site about the size of a half dollar) and VACCINATION SITE ERYTHEMA (hard red spot on the deltoid near the injection site about the size of a half dollar) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No treatment information was provided. Patient had hard red spot and it was barely raised.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No Medical History information was reported.
- Andere Medikamente
- VITAMINS NOS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 04.09.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient was administered the Moderna vaccine. patient is 15 years of age and should have received Pfizer vaccine. No adverse events or symptoms reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 01.09.2021
- Impfdatum
- 30.08.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
The pharmacist administered 1 mL instead of 0.5 mL on accident. The pharmacy receives the Pfizer shot syringes (1 mL) and Moderna syringes (3 mL). The pharmacy received new syringe products for 5 mL and the labeling and color looked nearly identical to the 3 mL syringe. Unfortunately, in a chaotically busy retail pharmacy, where patients want their vaccines and medications quickly. I was trying to be quick and administered the vaccines in a 5 mL syringe. The graduations in the 5 mL syringes are by 1 mL, so 1,2,3,4,5 mL. Each mL increases in increments of 0.2 mL, so 0.2, 0.4, 0.6, 0.8 and 1 mL. In the usual syringe, the first bold graduation is 0.5 mL (for the 3 mL syringe). In the 5 mL syringe, the first bold graduation is 1 mL. I have been administering covid vaccines since February 2021. By habit, I drew up the vaccine to the first bold mark, but regretfully, this was 1 mL instead of 0.5 mL. My pharmacy manager and I are working on eliminating all syringes that are not suitable for measuring volume for the covid vaccine. We receive Pfizer and Moderna shot supplies via a large box that is automatically sent from corporate/CDC (to my knowledge). My pharmacy manager and I are both confused on why we would be sent vaccine supplies that are not suitable for covid vaccinations to begin with. It is almost like they are trying to create a situation for a pharmacist to measure an incorrect dose. Although, it is ultimately my fault, I was placed in a hazardous situation, both with the work environment (due to short staffing and unrealistic expectations) and with the incorrect syringe supplies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 01.09.2021
- Impfdatum
- 30.08.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
The pharmacist administered 1 mL instead of 0.5 mL on accident. The pharmacy receives the Pfizer shot syringes (1 mL) and Moderna syringes (3 mL). The pharmacy received new syringe products for 5 mL and the labeling and color looked nearly identical to the 3 mL syringe. Unfortunately, in a chaotically busy retail pharmacy, where patients want their vaccines and medications quickly. I was trying to be quick and administered the vaccines in a 5 mL syringe. The graduations in the 5 mL syringes are by 1 mL, so 1,2,3,4,5 mL. Each mL increases in increments of 0.2 mL, so 0.2, 0.4, 0.6, 0.8 and 1 mL. In the usual syringe, the first bold graduation is 0.5 mL (for the 3 mL syringe). In the 5 mL syringe, the first bold graduation is 1 mL. I have been administering covid vaccines since February 2021. By habit, I drew up the vaccine to the first bold mark, but regretfully, this was 1 mL instead of 0.5 mL. My pharmacy manager and I are working on eliminating all syringes that are not suitable for measuring volume for the covid vaccine. We receive Pfizer and Moderna shot supplies via a large box that is automatically sent from corporate/CDC (to my knowledge). My pharmacy manager and I are both confused on why we would be sent vaccine supplies that are not suitable for covid vaccinations to begin with. It is almost like they are trying to create a situation for a pharmacist to measure an incorrect dose. Although, it is ultimately my fault, I was placed in a hazardous situation, both with the work environment (due to short staffing and unrealistic expectations) and with the incorrect syringe supplies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 01.09.2021
- Impfdatum
- 30.08.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
The pharmacist administered 1 mL instead of 0.5 mL on accident. The pharmacy receives the Pfizer shot syringes (1 mL) and Moderna syringes (3 mL). The pharmacy received new syringe products for 5 mL and the labeling and color looked nearly identical to the 3 mL syringe. Unfortunately, in a chaotically busy retail pharmacy, where patients want their vaccines and medications quickly. I was trying to be quick and administered the vaccines in a 5 mL syringe. The graduations in the 5 mL syringes are by 1 mL, so 1,2,3,4,5 mL. Each mL increases in increments of 0.2 mL, so 0.2, 0.4, 0.6, 0.8 and 1 mL. In the usual syringe, the first bold graduation is 0.5 mL (for the 3 mL syringe). In the 5 mL syringe, the first bold graduation is 1 mL. I have been administering covid vaccines since February 2021. By habit, I drew up the vaccine to the first bold mark, but regretfully, this was 1 mL instead of 0.5 mL. My pharmacy manager and I are working on eliminating all syringes that are not suitable for measuring volume for the covid vaccine. We receive Pfizer and Moderna shot supplies via a large box that is automatically sent from corporate/CDC (to my knowledge). My pharmacy manager and I are both confused on why we would be sent vaccine supplies that are not suitable for covid vaccinations to begin with. It is almost like they are trying to create a situation for a pharmacist to measure an incorrect dose. Although, it is ultimately my fault, I was placed in a hazardous situation, both with the work environment (due to short staffing and unrealistic expectations) and with the incorrect syringe supplies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 01.09.2021
- Impfdatum
- 30.08.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
The pharmacist administered 1 mL instead of 0.5 mL on accident. The pharmacy receives the Pfizer shot syringes (1 mL) and Moderna syringes (3 mL). The pharmacy received new syringe products for 5 mL and the labeling and color looked nearly identical to the 3 mL syringe. Unfortunately, in a chaotically busy retail pharmacy, where patients want their vaccines and medications quickly. I was trying to be quick and administered the vaccines in a 5 mL syringe. The graduations in the 5 mL syringes are by 1 mL, so 1,2,3,4,5 mL. Each mL increases in increments of 0.2 mL, so 0.2, 0.4, 0.6, 0.8 and 1 mL. In the usual syringe, the first bold graduation is 0.5 mL (for the 3 mL syringe). In the 5 mL syringe, the first bold graduation is 1 mL. I have been administering covid vaccines since February 2021. By habit, I drew up the vaccine to the first bold mark, but regretfully, this was 1 mL instead of 0.5 mL. My pharmacy manager and I are working on eliminating all syringes that are not suitable for measuring volume for the covid vaccine. We receive Pfizer and Moderna shot supplies via a large box that is automatically sent from corporate/CDC (to my knowledge). My pharmacy manager and I are both confused on why we would be sent vaccine supplies that are not suitable for covid vaccinations to begin with. It is almost like they are trying to create a situation for a pharmacist to measure an incorrect dose. Although, it is ultimately my fault, I was placed in a hazardous situation, both with the work environment (due to short staffing and unrealistic expectations) and with the incorrect syringe supplies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 01.09.2021
- Impfdatum
- 30.08.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
The pharmacist administered 1 mL instead of 0.5 mL on accident. The pharmacy receives the Pfizer shot syringes (1 mL) and Moderna syringes (3 mL). The pharmacy received new syringe products for 5 mL and the labeling and color looked nearly identical to the 3 mL syringe. Unfortunately, in a chaotically busy retail pharmacy, where patients want their vaccines and medications quickly. I was trying to be quick and administered the vaccines in a 5 mL syringe. The graduations in the 5 mL syringes are by 1 mL, so 1,2,3,4,5 mL. Each mL increases in increments of 0.2 mL, so 0.2, 0.4, 0.6, 0.8 and 1 mL. In the usual syringe, the first bold graduation is 0.5 mL (for the 3 mL syringe). In the 5 mL syringe, the first bold graduation is 1 mL. I have been administering covid vaccines since February 2021. By habit, I drew up the vaccine to the first bold mark, but regretfully, this was 1 mL instead of 0.5 mL. My pharmacy manager and I are working on eliminating all syringes that are not suitable for measuring volume for the covid vaccine. We receive Pfizer and Moderna shot supplies via a large box that is automatically sent from corporate/CDC (to my knowledge). My pharmacy manager and I are both confused on why we would be sent vaccine supplies that are not suitable for covid vaccinations to begin with. It is almost like they are trying to create a situation for a pharmacist to measure an incorrect dose. Although, it is ultimately my fault, I was placed in a hazardous situation, both with the work environment (due to short staffing and unrealistic expectations) and with the incorrect syringe supplies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 31.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heavy menstrual bleeding
Hypoaesthesia
Symptomtext
Excessive heavy bleeding with menstrual period lasting several days. Also numbness on her left side From jaw to leg) starting on 8/31/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heavy menstrual bleeding
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Flu shot arm reaction
- Staat
- OH
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 07.08.2021
- Beginn
- 07.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Got 1 dose of moderna vaccine after completing the vaccination series with J&J vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of INTERCHANGE OF VACCINE PRODUCTS (Got 1 dose of moderna vaccine after completing the vaccination series with J&J vaccine) in an 85-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 049E21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Aug-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Got 1 dose of moderna vaccine after completing the vaccination series with J&J vaccine). On 07-Aug-2021, INTERCHANGE OF VACCINE PRODUCTS (Got 1 dose of moderna vaccine after completing the vaccination series with J&J vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment information was provided. On an unknown date in Mar-2021, the patient completed vaccination series with J & J COVID-19 vaccine. On 07-Aug-2021, the patient was supposed to get COVID-19 test done. Instead of the COVID test, the patient got first dose of the moderna COVID-19 vaccine. The patient was currently doing fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 26.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nervous system disorder
Symptomtext
She has severe neurological issues that are many
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nervous system disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Dormant lymes disease
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 26.08.2021
- Impfdatum
- 24.08.2021
- Beginn
- 25.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Extra dose administered
Symptomtext
pt states abnormal red spots that appear on both her feet following the 3rd dose of the covid vaccine (moderna). no other issues at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 25.08.2021
- Impfdatum
- 25.08.2021
- Beginn
- 25.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injury associated with device
Symptomtext
Immunizer had a needle stick injury after the vaccination was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injury associated with device
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 17.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Blepharospasm
Eye movement disorder
Hypoaesthesia oral
Mydriasis
Symptomtext
tongue is numb, loss of taste, right eye does not close fully and twitches, and pupil is dilated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ageusia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 20.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Interchange of vaccine products
Symptomtext
Patient completed online vaccine consent form for Moderna 3 (booster). I verified in the vaccine room that patient was requesting the vaccine Moderna. After vaccine was administered patient presented vaccine card which stated she got her first 2 doses of Pfizer at a pharmacy. I then explained to patient she should have received Pfizer, patient stated she wanted Moderna. She stated she had heard information that Moderna was a better option. Patient stated the vaccine we administered is the one she wanted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 20.08.2021
- Impfdatum
- 14.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Symptomtext
Patient states arm was swollen to the width of her hand
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Peripheral swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 18.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Pt's parent presented to pharmacy showing me her son's CDC card which indicated pt rec'd FIRST MODERNA dose at another facility in January 2021. Pt is disabled and in a wheelchair so I did not necessarily look at pt to gauge age. I did make a copy of the parent's driver's license but not the patient's ID. The pharmacy grad intern administered the actual vaccine and I only realized the error later that evening when I was processing the pt's vaccine through insurance for billing purposes, per standard practice at .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 17.08.2021
- Impfdatum
- 17.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
vaccine was given at 20 days instead of 28 due to error in grits and system not catching early fill.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 17.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Interchange of vaccine products
Symptomtext
Patient received 1st and 2nd dose of Pfizer at another location. He received 3rd covid vaccine (Moderna).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Metformin, Atorvastatin, Lisinopril-HCTZ
- Allergien
- None listed
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 14.08.2021
- Impfdatum
- 14.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
No adverse event
Symptomtext
Patient received Janssen COVID-19 vaccine on March 5, 2021. She had reported she never received a COVID-19 vaccine in the past and the dose was given. Patient had no reaction in 15 minute wait period.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 13.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 13.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Interchange of vaccine products
Symptomtext
customer received JJ vaccine at another facility on 3/12/2021 and did not told us she had a vaccine of another manufacturer . we found out from the insurance when we try to bill . finally she admitted she had the JJ vaccine but her doctor told her to get another dose of another manufacturer .
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
- -
- Staat
- NC
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 12.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
When patient came in for her vaccine appointment, I asked her if this would be her first or second dose. She replied that this would be her first dose. I next asked her, if she ever received a dose from another manufacturer or any other dose from anywhere ever. She replied that she did not and that this would be her first dose. When I went to go enter her info into the system, I noticed that she did in fact receive 2 doses of Moderna from Health Department. Next, I tried to call her to discuss this with her and the number she gave me did not work.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- not necessary
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- asthma
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 12.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Muscle twitching
Symptomtext
6-8 hours after receiving vaccination body began twitching, began to subside after a couple of hours. Twitching has reoccurred.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Muscle twitching
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 10.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Swelling of eyelid
Symptomtext
adverse events: this morning the patient woke up with swollen eyelids and swollen lips
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -