- Staat
- NY
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 09.11.2023
- Impfdatum
- 30.09.2023
- Beginn
- 30.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Hypoaesthesia
C-reactive protein
Differential white blood cell count
Dysstasia
Fall
Full blood count
Gait inability
Immunisation reaction
Metabolic function test
Red blood cell sedimentation rate
Respiratory pathogen panel
Urine analysis
Syncope
Symptomtext
Injection occurred around 2:20pm on 9/30/2023. Symptoms of lower body numbness started later that day around 5pm. Pt went to emergency room and according to pt., he had blood work, blood pressure done and waited until 9:30 at which time he was discharged because they could not diagnose causation and told pt. to go to primary care provider as soon as possible. Pt contacted Dr and she referred him to another doctor. 3 days later pt saw Dr
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- unknown other than what was already reported by patient
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- diabetes, gout, uncontrolled hypertension, 3 stents, watchman pacemaker, severe neuropathy
- Andere Medikamente
- Losartan, allopurinol, atorvastatin, potassium citrate, metformin, sotalol, isosorbide, spironolactone
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 18.05.2023
- Beginn
- 31.05.2023
- Tage bis Beginn
- 13,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: ja
Angiocardiogram
Chest X-ray
Computerised tomogram abdomen
Computerised tomogram head
Computerised tomogram thorax
Echocardiogram
Electromyogram
Endotracheal intubation
Guillain-Barre syndrome
Immunoglobulin therapy
Intensive care
Magnetic resonance imaging spinal
Plasmapheresis
Pneumonia aspiration
Respiratory failure
Symptomtext
Acute inflammatory demyelinating polyneuropathy or Guillain-Barre causing subsequent respiratory failure and aspiration pneumonia Leading to long hospitalization ICU stay intubation for 5 days 5 doses of IVIG and 5 episodes of plasmapheresis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- 48,0
- Labordaten
- MRI cervical, thoracic, and lumbar spine, EMG times two, ECHO, multiple chest xrays, CTA chest, CT abdominal/pelvis, CT chest, CT brain
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Prediabetes, hypertension, hyperlipidemia, non-alcoholic fatty liver, obesity
- Andere Medikamente
- ibuprofen, omega 3 fatty acids, olmesartan, rosuvastatin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 05.10.2023
- Impfdatum
- 03.10.2023
- Beginn
- 04.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
patient fainted the day following receiving the vaccinations. patient is okay
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 04.08.2023
- Beginn
- 04.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abnormal sleep-related event
Alanine aminotransferase normal
Anion gap
Aspartate aminotransferase normal
Basophil count normal
Basophil percentage decreased
Blood albumin normal
Blood alkaline phosphatase normal
Blood bicarbonate
Blood bilirubin decreased
Blood calcium normal
Blood chloride increased
Blood creatine phosphokinase normal
Blood creatinine normal
Blood glucose normal
Blood magnesium
Blood phosphorus decreased
Blood potassium normal
Symptomtext
Patient was sleeping when his brother noticed that he was snoring and acting "different" in his sleep as normal. Patient woke up and felt off. He had blood pressure checked and was high. Does not remember values.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- ER visit 8/4/2023 Creatine Kinase 30 - 225 U/L 103 Phosphorus Level 2.5 - 4.5 mg/dL 2.4 Low Magnesium Level 1.6 - 2.5 mg/dL 2.3 Sodium Level 134 - 146 mmol/L 139 Potassium Level 3.4 - 5.0 mmol/L 4.1 Chloride 98 - 112 mmol/L 107 HCO3 21 - 29 mmol/L 22 Anion Gap 9 - 18 mmol/L 10 Glucose Level 70 - 99 mg/dL 104 High Blood Urea Nitrogen 8 - 20 mg/dL 14 Creatinine 0.60 - 1.30 mg/dL 0.74 CKD-EPI >=60 mL/min/1.73 m2 >90 Comment: CKD-EPI estimated GFR (eGFR) calculation is based on the 2021 CKD-EPI equation. New Creatinine- and Cystatin C-Based Equations to Estimate GFR without Race. CKD-EPI eGFR is best used for detection of chronic kidney disease in clinically stable patients. DO NOT USE VALUES FROM THIS EQUATION FOR DRUG DOSING. It has not yet been validated for drug dosing or for patients with rapidly changing clinical situations (inpatient care). CG eCrCl Calcium Level Total 8.6 - 10.4 mg/dL 9.3 Protein Total 6.0 - 8.0 g/dL 7.2 Albumin Level 3.5 - 5.2 g/dL 4.6 Bilirubin Total 0.2 - 1.0 mg/dL 0.2 Alkaline Phosphatase 40 - 129 IU/L 91 ALT w/ P5P 0 - 50 IU/L 39 AST w/ P5P 0 - 50 IU/L 25 White Blood Cell 4.00 - 10.80 x10*3/uL 15.55 High Red Blood Cell 4.60 - 6.00 x10*6/uL 5.10 Hemoglobin 14.0 - 18.0 g/dL 15.2 Hematocrit 42.0 - 52.0 % 45.0 Mean Cell Volume 80.0 - 100.0 fL 88.2 Mean Cell Hemoglobin 27.0 - 33.0 pg 29.8 Mean Cell Hemoglobin Concentration 32.0 - 37.0 g/dL 33.8 Red Cell Diameter Width 11.0 - 16.0 % 12.3 NRBC Absolute Count 0.00 - 0.01 x10*3/uL 0.00 NRBC Automated 0.0 - 0.1 %WBC 0.0 Platelet 140 - 400 x10*3/uL 234 Mean Platelet Volume 7.4 - 11 fL 10.6 Neutrophil Automated 35.0 - 80.0 % 80.9 High Immature Granulocyte Automated 0.0 - 0.6 % 0.7 High Lymphocyte Automated 20.0 - 50.0 % 12.2 Low Monocytes Automated 2.0 - 12.0 % 4.8 Eosinophil Automated 0.0 - 6.0 % 1.1 Basophil Automated 0.0 - 2.0 % 0.3 Neutrophil Absolute Count 1.80 - 7.80 x10*3/uL 12.57 High Immature Granulocyte Absolute Count 0.00 - 0.05 x10*3/uL 0.11 High Lymphocyte Absolute Count 1.00 - 4.00 x10*3/uL 1.90 Monocyte Absolute Count 0.00 - 0.90 x10*3/uL 0.75 Eosinophil Absolute Count 0.00 - 0.50 x10*3/uL 0.17 Basophil Absolute Count 0.00 - 0.20 x10*3/uL 0.05
- Aktuelle Erkrankungen
- No known illnesses at time or before immunization administered.
- Vorgeschichte
- No chronic or long-standing health conditions.
- Andere Medikamente
- No prescriptions, OTC, dietary supplements or herbal supplements taken before, on or after immunization given.
- Allergien
- No known allergies to medications, food or other products.
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 24.09.2023
- Impfdatum
- 21.09.2023
- Beginn
- 21.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Decreased appetite
Dizziness
Dyspnoea
Gait disturbance
Injection site erythema
Malaise
Migraine
Nausea
Tinnitus
Symptomtext
Patient states that after receiving these vaccines she became ill around 7 hours later. She described her symptoms as migraine headache, shortness of breath, red injection sites, ringing in the ears, light headedness, trouble walking, joint pain, nausea, and a lack of appetite. Patient states that she took 600 mg of Ibuprofen. She states she considered going the Emergency room but did not. Patient states she is still pretty wiped out but seems to be getting better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- azithromycin, morphine, oxycodone, quinolones
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 14.09.2023
- Impfdatum
- 01.09.2023
- Beginn
- 01.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Chest pain
Dysgeusia
Electrocardiogram
Facial pain
Blood test
Ear pain
Eye irritation
Fatigue
Headache
Hypoaesthesia
Oral discomfort
Tinnitus
Immediate post-injection reaction
Inappropriate schedule of product administration
Injection site pain
Laboratory test
Myalgia
Symptomtext
Headaches; Numbness on one side of the head; Ears were whistling; Ear was irritated specially left one; Mouth was burning; Feeling very tired / Lot of fatigue; Irritated eyes; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old male patient received pneumococcal 20-valent conjugate vaccine (diphtheria CRM197 protein) (PREVNAR 20), on 01Sep2023 as dose number unknown, single (Batch/Lot number: unknown) at the age of 69 years, in left arm for immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Prevnar 13, administration date: Aug2022, for immunization. The following information was reported: EAR PAIN (non-serious) with onset Sep2023, outcome "not recovered", described as "Ear was irritated specially left one"; TINNITUS (non-serious) with onset Sep2023, outcome "not recovered", described as "Ears were whistling"; FATIGUE (non-serious) with onset Sep2023, outcome "unknown", described as "Feeling very tired / Lot of fatigue"; HEADACHE (non-serious) with onset Sep2023, outcome "unknown", described as "Headaches"; EYE IRRITATION (non-serious) with onset Sep2023, outcome "not recovered", described as "Irritated eyes"; ORAL DISCOMFORT (non-serious) with onset Sep2023, outcome "recovering", described as "Mouth was burning"; HYPOAESTHESIA (non-serious) with onset Sep2023, outcome "unknown", described as "Numbness on one side of the head". The events "headaches", "numbness on one side of the head", "ears were whistling", "ear was irritated specially left one", "mouth was burning" and "feeling very tired / lot of fatigue" required emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient had Prevnar 20 on Friday, 01Sep2023 and the reactions were very awful. When the patient got the Prevnar 20, he experienced headaches, numbness on one side of the head, ears were whistling, ear was irritated specially left one, his mouth was burning, he was feeling very tired with a lot of fatigue. So, he went back to see the doctor but he was sent to the Nurse and the Nurse sent him to the emergency room (ER). At the emergency room, they did some lab work about five or six blood samples. The patient still has the symptoms, it has been over a week, but he still has the whistling sound in his ear. He still has irritated eyes. The burning in mouth went away but not completely. So, nobody was helping him because they do not seem to think this is an emergency, it does not help out. He wanted someone to take care of the symptoms that he got because it has been over a week. The information on the batch/lot number pneumococcal 20-valent conjugate vaccine (diphtheria CRM197 protein) has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Name: lab work; Result Unstructured Data: Test Result:Unknown Results; Comments: they did some lab work, they did five or six blood samples
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 10.09.2023
- Impfdatum
- 08.09.2023
- Beginn
- 08.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysphemia
Hemiplegia
Malaise
Paraesthesia
Symptomtext
Patients sister reported the patient was sick since about two hours after receiving the vaccines. Sister was convinced it was the RSV vaccine that caused all of the symptoms but flu was given in the right arm. Sister reported patient has tingling in her right arm then then proceeded to go her entire right side, right side paralysis, and stuttering as reported to her by the patient's husband at about 3:30 AM this morning. Patient was evaluated at ER and is home but really ill.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- cancer
- Vorgeschichte
- cancer
- Andere Medikamente
- oxycodone lorazepam hydroxyzine HCl Konvomep diphenox/atropine ondansetron gabapentin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 16.06.2023
- Impfdatum
- 13.06.2023
- Beginn
- 15.06.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Musculoskeletal discomfort
Paraesthesia
Symptomtext
experiencing shoulder, elbow and finger discomfort. Tingling in the fingers. Has experienced this in the past but not sure if it directly correlates with the vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma
- Andere Medikamente
- oxybutynin er 15mg, metoprolol 25, pantoprazole 40, tamsulosin 0.4mg, buspirone 5mg, seroquel 50ng, clonazepam 0.5mg, montelukast 10mg, gabapentin 300mg, loratadine 10, symbicort 160, vitamin d3, docusate 100mg
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 05.11.2023
- Impfdatum
- 18.10.2023
- Beginn
- 18.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site cellulitis
Injection site erythema
Injection site swelling
Injection site warmth
Local reaction
Symptomtext
Patient came in on 11/5/23 and reports they had an adverse reaction to possibly the arexvy vaccine recieved on 10/18/23. Patient reports they experienced some local injection site reactions on the same evening of 10/18/23. On 10/19/23, patient reports it was red, hot to the touch and raised slightly and it was slightly bigger than previously. On 10/20/23, patient reports that the reaction was from the deltoid muscle to the elbow and had wrapped around three-quarters around. Patient the was given bactrim DS for 7 days for cellulitis starting on 10/20/23. On 10/22/23, patient reports relief and reduction in size of reaction. Patient reported no fever nor any systemic symptoms for the duration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Neurologic Disorder, complex regional pain syndrome, ADHD, dysautonomia, migraine, GERD-related laryngitis, asthma
- Andere Medikamente
- -
- Allergien
- Iodinated Contrast Media, tramadol, tiotropium, montelukast, codeine, penicillin, latex
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 19.10.2023
- Impfdatum
- 14.09.2023
- Beginn
- 17.09.2023
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Erythema
Inflammation
Injection site pruritus
Injection site swelling
Peripheral swelling
Symptomtext
Patient received the Prevnar vaccine 9/14. She then noticed a red bump on her right arm the following Sunday, 9/17. Over the next days, it extended to wrap around her right upper arm. It was itchy and swollen, not painful. She was having some chills on Monday 9/18, but didn't take her temperature. Did not persist into Tuesday. No body aches. No shortness of breath. She has tried topical hydrocortisone without help. She was taking Tylenol and Advil to help reduce inflammation. No known allergies to vaccinations or their ingredients. Patient was started on cefadroxil and reported improvement in symptoms. Has since resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- monoclonal B-cell lymphocytosis progressing to CLL
- Vorgeschichte
- ? Atrial fibrillation 12/21/2010 ? AV nodal re-entry tachycardia 12/16/2008 ? Basal cell carcinoma ? Benign hypertension 6/22/2011 ? CLL (chronic lymphocytic leukemia) 2008 ? Congestive heart failure 8/13/1999 ? Ectopic atrial tachycardia -near phrenic nerve 2/18/2019 ? Grover's disease 2020 ? History of radiofrequency ablation (RFA) procedure for cardiac arrhythmia-aborted due to phrenic nerve location 2/18/2019 December 18th, 2018 ? Hypertension 12/8/2006 ? Mobitz type 1 second degree AV block 5/5/2003 ? Premature ventricular contraction 11/10/2004, 6/29/2012 ? S/P catheter ablation of slow pathway 1990 ? Squamous cell cancer of skin of eyebrow 01/13/2020 ? Supraventricular tachycardia 12/4/2008 ? Thyroid disease
- Andere Medikamente
- ? amiodarone (PACERONE) 200 mg tablet Take 1 tablet (200 mg total) by mouth 1 (one) time a day. ? candesartan (ATACAND) 16 mg tablet Take 1 tablet (16 mg total) by mouth 1 (one) time a day. ? cefadroxil (DURICEF) 500 mg capsule Take 1 capsu
- Allergien
- ? Bactrim [Sulfamethoxazole-Trimethoprim] Nausea ? Benazepril Cough ? Erythromycin Nausea ? Trimethoprim (Bulk) Reaction unknown
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 25.09.2023
- Impfdatum
- 22.09.2023
- Beginn
- 23.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cellulitis
Feeling hot
Pain
Symptomtext
Patient had cellulitis in the injection arm. Went to Urgent Care and got Keflex, Medrol Dosepack and clobetasol. Feeling warm and pain. Started the next day of the vaccination and progressed. Went to Urgent Care 2 days after the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Prevnar 20 was given at the same time
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 25.09.2023
- Impfdatum
- 21.09.2023
- Beginn
- 22.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Diarrhoea
Erythema
Malaise
Peripheral swelling
Symptomtext
Patient's daughter states the patient has a red arm, swollen, and experienced diarrhea and not feeling will starting approximately on Friday
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 23.09.2023
- Impfdatum
- 19.09.2023
- Beginn
- 19.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Musculoskeletal stiffness
Pain
Symptomtext
Spoke w/ patient. She received Fluzone HD and Prevnar20 on the same arm on 9/19. She wanted them in the same arm because she didn't want both arms to be sore. She says she began having soreness later that day and it progressed to a stiff neck (she's having trouble moving the neck). It's begun to get better, but she wasn't sure if it was related to the vaccination. We discussed that going forward, we should avoid more than 1 vaccine at a time and possibly consider Flublok or regular dose Fluzone instead of Fluzone HD. She said she just wanted to report it, is not seeking any compensation or further care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 19.09.2023
- Impfdatum
- 11.08.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Pain in extremity
Vaccination site erythema
Vaccination site pain
Vaccination site pruritus
Vaccination site swelling
Symptomtext
injection site reaction of pain, swelling and itching; injection site reaction of pain, swelling and itching; injection site reaction of pain, swelling and itching; site where she got vaccine is red; painful on the inside of her arm; This is a spontaneous report received from contactable reporter (Other HCP) from medical information team. A 49-year-old female patient received pneumococcal 20-val conj vac (dipht crm197 protein) (PREVNAR 20), on 11Aug2023 as dose number unknown, 0.5ml single (Lot number: GN1898, Expiration Date: 30Sep2024) at the age of 49 years intramuscular, in left deltoid for immunisation. The patient's relevant medical history included: "Diabetes", start date: Jun2022 (unspecified if ongoing); "Hypothyroidism", start date: Jun2022 (unspecified if ongoing); "hypertensive disorder", start date: 11Aug2023 (unspecified if ongoing); "Anemic", start date: Jul2022 (unspecified if ongoing). Concomitant medication(s) included: TDAP intramuscular taken for immunisation, on 11Aug2023 as dose number unknown, 0.5ml single. The following information was reported: VACCINATION SITE PAIN (non-serious), VACCINATION SITE SWELLING (non-serious), VACCINATION SITE PRURITUS (non-serious), outcome "unknown" and all described as "injection site reaction of pain, swelling and itching"; VACCINATION SITE ERYTHEMA (non-serious), outcome "unknown", described as "site where she got vaccine is red"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "painful on the inside of her arm". The events "injection site reaction of pain, swelling and itching", "site where she got vaccine is red" and "painful on the inside of her arm" required physician office visit. The information on the batch/lot number for pneumococcal 20-val conj vac (dipht crm197 protein) has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anemic; Diabetes; Hypertensive; Hypothyroidism
- Andere Medikamente
- TDAP
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 19.09.2023
- Impfdatum
- 13.09.2023
- Beginn
- 15.09.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Injection site erythema
Injection site pain
Injection site warmth
Myalgia
Nausea
Pyrexia
Symptomtext
The day after the patient developed fevers, chills, nausea, and muscle/joint pains. Two days later she developed a large, red patch just inferior to the injection site. The site is red, hot, and painful. The area is very discrete.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 18.09.2023
- Impfdatum
- 02.09.2023
- Beginn
- 03.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Diarrhoea
Headache
Oropharyngeal pain
Symptomtext
Patient received 4 vaccines- Prevnar 20, Arexvy, FluzoneHD, and pfizer bivalent on 9/2/23. She reported on 9/17/23 that she had side effects the next day. The patient experienced headache, diarrhea, sore throat, and cough. Pt believes these side effects were due to the Arexvy since she has never had side effects with any of the other vaccines before. Patient stated she had these side effects for about 1 week, she has recovered from them by now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 16.09.2023
- Impfdatum
- 14.09.2023
- Beginn
- 15.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site nodule
Injection site swelling
Injection site warmth
Symptomtext
pt has warm, raised red nodule at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 30.08.2023
- Impfdatum
- 23.08.2023
- Beginn
- 24.08.2023
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injection site erythema
Injection site mass
Injection site pruritus
Injection site swelling
Injection site warmth
Pruritus
Symptomtext
Raised swollen red lump on left arm with localized itching and heat at site. Patient reported via electronic message system. Patient was contacted by triage nurse and scheduled with provider in clinic. Patient cancelled appt with provider.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- dizziness, fatigue , muscle weakness
- Vorgeschichte
- Type 1 diabetes , hypothyroidism, Ankylosing spondylitis
- Andere Medikamente
- cholecalciferol, vitamin D3, (VITAMIN D3 ORAL) Take by mouth insulin aspart U-100 (NOVOLOG FLEXPEN, U-100,) 100 unit/mL (3 mL) Up to 24 units LANTUS SOLOSTAR U-100 INSULIN 100 unit/mL (3 mL) 10-12 units levonorgestreL (MIRENA) 20 mcg/
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 05.08.2023
- Impfdatum
- 04.08.2023
- Beginn
- 04.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Musculoskeletal stiffness
Pain in extremity
Skin warm
Symptomtext
Patient reports arm pain, stiffness, burning and hot to the touch starting the evening of adminstration and continuing into the following day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 30.07.2023
- Impfdatum
- 25.07.2023
- Beginn
- 26.07.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Fatigue
Hypersomnia
Injection site rash
Pain in extremity
Pyrexia
Symptomtext
PATIENT STATED SHE FELT VERY TIRED, FEVERISH, PAINFUL ARM, AND SLEPT A LOT FOR A FEW DAYS. SHE NOTICED THE RASHES ON THE LEFT UPPER ARM THE MORNING AFTER VACCIEN GIVEN. SHE WENT TO THE EMERGENCY DEPARTMENT ON 07-30-2023 AND RECEIVED TREATMENT AND SENT HOME WITH SOME PRESCRIPTIONS. SHE IS NOW STATBLE AND RESTING. SHE WILL BE FOLLOWING UP WITH HER PCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- PATIENT DID NOT NOTIFY OR RETURNED TO THE PHARMACY UNTIL TODAY 07-30-2023.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HIGH CHOLESTEROL. HIGH BLOOD SUGAR. INDIGESTION. SEASONAL ALLERGY.
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 17.07.2023
- Impfdatum
- 12.07.2023
- Beginn
- 12.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Pain
Pyrexia
Symptomtext
Subjective fever x3d, chills, body aches. Sx's are resolving at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- PAD, HLD, Hx of bladder Ca, Hx of BLE amputations
- Andere Medikamente
- Gabapentin, Acetaminophen, Plavix, Atorvastatin,Famotidine
- Allergien
- Bactrim, morphine, erythromycin, Cephalexin
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 05.07.2023
- Impfdatum
- 29.06.2023
- Beginn
- 30.06.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Rash pruritic
Symptomtext
Itchy rash at injection site. Used hydrocortisone cream and it is relieving. Pt didn't need medical attention and didn't think he needed to call his doctor. Unsure of when rash officially started so just put the day after but pt should be able to answer that if contacted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- received Pfizer Bivalent Covid-19 vaccine in same arm on the same day but reports no issue with this vaccine previously, as this was his 2nd dose.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 30.06.2023
- Impfdatum
- 28.06.2023
- Beginn
- 29.06.2023
- 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 urticaria
Symptomtext
hives at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- allergic rhinitis
- Vorgeschichte
- glaucoma hypothyroidism
- Andere Medikamente
- latanoprost levothyroxine triamcinolone 1% cream
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 26.06.2023
- Impfdatum
- 20.06.2023
- Beginn
- 22.06.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Pain in extremity
Peripheral swelling
Pruritus
Pyrexia
Symptomtext
Arm was swollen, painful, red, itchy including palms with patient reporting low fevers that lasted up to six days after the vaccination on 6/20/2023. The patient reports that the swelling, redness and pain are resolving as of 6/26/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None required.
- Aktuelle Erkrankungen
- hemoptysis in patient with recent positive quantiferon blood test (CT scan scheduled 6/30/2023 to r/o LTBI) with weight loss.
- Vorgeschichte
- Moya Moya, pre diabetes, hyperlipidemia, pre diabetes, HTN, chronic headaches. COPD
- Andere Medikamente
- Vitamin D 25 mcq, Albuterol HFA 90 mcq, amlodipine 5 mg, atorvastatin 20 mg, advair 250/50 mcq, monteclast 10 mg.
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 22.06.2023
- Impfdatum
- 16.06.2023
- Beginn
- 21.06.2023
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site rash
Injection site reaction
Pain in extremity
Wound
Symptomtext
Patient presents to clinic with red rash estimated 4x2inch rash on right deltoid. History as follows: Vaccine given 06/16/2023. Tenderness noted at right deltoid from 16th - 21st 06/21/2023 afternoon noted small, non-discolored bumps at the site. Itchiness at site. Patient applied cortisone cream at home and this helped. Today patient noted red rash of 4x2 inch area. Bumps resolved. Outside of wound is itchy. Whole arm aches. site is tender. Kenalog cream and claritin oral ordered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No other illness
- Vorgeschichte
- Hyperlipidemia, Overweight, Prolapse of vaginal wall
- Andere Medikamente
- Vitamin C, Vitamin D, Benadryl as needed, Flonase, Lactobacillus, Ativan as needed, Magnesium Citrate, Omeprazole
- Allergien
- Cats allergies
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 21.06.2023
- Impfdatum
- 19.06.2023
- Beginn
- 20.06.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Rash
Rash erythematous
Rash macular
Rash pruritic
Symptomtext
Per Patient "Last evening I developed a mild rash, mostly on my arms and torso. Pink, splotchy and itchy. Also a headache. I called the nurse advisor to discuss. Because I was scheduled for a bone density this morning I didn't take any benedryl as it contains calcium, but used topical Cortisone 10. This morning the rash as almost entirely gone. The nurse advisor suggested that I advise you since it was possibly a reaction to the pneumonia shot. I had eaten shrimp for dinner but have never had any reactions to shellfish in the past. Nurse advisor couldn't find any connection between the vaccine and shellfish. I still have a mild headache but otherwise okay."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Left total knee arthroplasty 8 weeks ago. Slow recovery. Recently prescribed prednisone taper (finished on 6/13/23)
- Vorgeschichte
- Raynaud's disease History of hyperlipidemia History of elevated glucose BMI 28.0-28.9, adult Acquired hypothyroidism SUI (stress urinary incontinence, female) DES exposure in utero Long term use of non-steroidal anti-inflammatories Fibromyalgia Erosive Osteoarthritis Primary osteoarthritis of left knee
- Andere Medikamente
- acetaminophen 1,000 mg q 6 hours PRN Probiotic 1 tablet daily vitamin D3 2,000 units daily vitamin B12 2,000 mcg 3 times per week ibuprofen 400 mg TID PRN levothyroxine 75 mcg daily magnesium oxide 500 mg daily melatonin 10 mg at bedtime PR
- Allergien
- Aciphex (Rabeprazole) Adhesive Bandage Adhesive Tape Dye Nexium (Esomeprazole Magnesium) 2-octyl Cyanoacrylate
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 16.06.2023
- Impfdatum
- 14.06.2023
- Beginn
- 15.06.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Fatigue
Feeling hot
Hair disorder
Headache
Joint range of motion decreased
Myalgia
Nausea
Pyrexia
Swelling
Vomiting
Symptomtext
Redness, swelling, heat, pain, decreased range of motion, fever, chills, myalgia, fatigued, headache, nausea w/o emesis, "My hair hurts"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- NONE YET
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- Patient Active Problem List Diagnosis Date Noted POA ? Advanced care planning/counseling discussion 06/14/2023 Unknown ? Healthcare maintenance 03/27/2021 Unknown ? Encounter for screening for lung cancer 03/17/2021 Unknown ? Osteopenia 03/17/2021 Unknown ? Injury of right thumb 09/12/2014 Unknown ? HTN (hypertension) 01/15/2013 Unknown ? Degenerative disc disease, cervical 12/12/2012 Unknown ? Cervical spondylosis 11/21/2012 Unknown ? Lesion of left ulnar nerve 08/16/2012 Unknown ? Injury of left thumb 03/15/2012 Unknown ? Knee pain 11/21/2011 Unknown ? Tobacco abuse 11/21/2011 Unknown ? Chronic low back pain 10/03/2011 Unknown ? Hyperlipidemia 10/03/2011 Unknown ? Obesity 10/03/2011 Unknown ? Osteoarthrosis 10/03/2011 Unknown
- Andere Medikamente
- Atorvastatin 10mg, Medical Cannabis BID, Telmisartan- amlodipine 40-5 mg, Trazodone 50 mg
- Allergien
- Meloxicam
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 07.06.2023
- Impfdatum
- 23.05.2023
- Beginn
- 25.05.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cough
Injection site bruising
Injection site erythema
Injection site pruritus
Injection site swelling
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: cough-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 06.06.2023
- Impfdatum
- 30.05.2023
- Beginn
- 04.06.2023
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Injection site erythema
Injection site swelling
Injection site warmth
Lymph node pain
Lymphadenopathy
Nausea
Peripheral swelling
Pyrexia
Symptomtext
Lymph node on my collar bone on the left side was very swollen and now the area where I got the shot is very red and hot and swollen and my arm and several lymph nodes on the left side are swollen and painful. feeling very exhausted, nauseated, fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none at this time
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Type 2 diabetes, PCOS, fatty liver, htn
- Andere Medikamente
- acetaminophen (TYLENOL) 500 mg tablet Sig: Take 2 tablets by mouth every 6 hours as needed for Pain or Headaches. Class: Historical Med Route: Oral AIMOVIG 70 MG/ML injection 1 mL 11 5/6/2023 Sig: INJECT 1ML UNDER THE SKIN EVERY 30 DAY
- Allergien
- Thiazide-type Diuretics 05/18/2015 Contraindication Other (See Comments) PANCREATITIS Doxycycline 12/14/2010 Unspecified Diarrhea, Nausea And Vomiting, Hives, Nausea Only, Rash Ketorolac 12/13/2016 Intolerance Anxiety, Other (See Comments) Panic reaction Venlafaxine 12/13/2016 Intolerance Anxiety, Other (See Comments) Sleep problems
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 05.06.2023
- Impfdatum
- 02.06.2023
- Beginn
- 03.06.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Pain in extremity
Symptomtext
On saturday morning, the day after vaccines, patient went outside to take her dog for a walk. Her arms were sore, so she swung them around 'windmill style. ' She said she then felt both her legs go numb and had to sit down. It lasted about 10 minutes. After 10 minutes, her legs felt better. She took it 'easy' the rest of the day and is ok now. She did not seek medical attention, but called to report to pharmacy and her primary doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- hypothyroid, high cholesterol, impaired fasting glucose
- Andere Medikamente
- Levothyroxine, Victoza, Pravastatin, Escitalopram
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 01.06.2023
- Impfdatum
- 30.05.2023
- Beginn
- 01.06.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Skin warm
Symptomtext
Patient asked about a rash on arm a few inches below injection site that extended to bend in arm. Rash appeared to be slightly larger than a dollar bill. They stated it was warm to touch but did not itch. They were recommended to apply cold compress and follow up at scheduled visit with primary care next day 6/2/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 30.05.2023
- Impfdatum
- 23.05.2023
- Beginn
- 24.05.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Bone pain
Ear discomfort
Ear pain
Feeling abnormal
Headache
Pain
Symptomtext
Pt presents to clinic due to feeling "weird" after receiving a vaccine on 05-23-2023. Pt states vaccine was given here. Pt was given PCV20. 12 hrs started hurting joints and bones, HA, left ear. Ibuprofen helped. Next day left ear worse, pressure, plugged. 5 days later right ear started to hurt also, right temple very sore. Unsupportable. Ibuprofen and bendryl helped him relax. Still feels very plugged. Feels like he is inside a bubble. Amoxicillin 500 mg tablet prescribed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HTN Obesity Derangement of left knee Mixed anxiety and depressive disorder prediabetes
- Andere Medikamente
- Current Medication: atorvastatin 80 mg tablet cyclobenzaprine 10 mg tablet ibuprofen 600 mg tablet lisinopriL 20 mg tablet Voltaren 1 % topical gel
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 25.05.2023
- Impfdatum
- 19.05.2023
- Beginn
- 19.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site induration
Injection site pain
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Red area size of softball, swollen, warm to touch, itchy, hard, and painful at site of injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HTN, DM type 2, obesity, GERD, depression, migraines, sleep apnea.
- Andere Medikamente
- Aspirin 81 mg, lipitor 10 mg, citalopram 40 mg, HCTZ 12.5 mg , lisinopril 40 mg, metformin 1000 mg BID.
- Allergien
- codeine, dust mites, tetanus vaccine
- Vorherige Impfungen
- rash, swelling, 1/7/2008 from tetanus vaccine, 31 yrs old
- Staat
- MA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 23.05.2023
- Impfdatum
- 17.05.2023
- Beginn
- 22.05.2023
- Tage bis Beginn
- 5,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Erythema
Induration
Pain in extremity
Pyrexia
Symptomtext
patient had initial achy arm, felt tactile fever, felt firmness and painful then got less painful but about day 4 more red and presented to clinic day 6 with continued worsening redness. treated for cellulitis given getting worse and day 6.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- exam
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- none
- Andere Medikamente
- B12, pepcid, simethicone
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 22.05.2023
- Impfdatum
- 15.05.2023
- Beginn
- 18.05.2023
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Erythema
Pain in extremity
Pruritus
Swelling
Symptomtext
pt states that itching and soreness started within a day, and 3 days later it began to swell and get red. it is 1 week later and the arm is still red, and sore but not as red as it was, and it's not itching like it was
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- diabetic
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 21.05.2023
- Impfdatum
- 15.05.2023
- Beginn
- 15.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pain
Injection site reaction
Injection site swelling
Injection site warmth
Symptomtext
Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: patient had a localized reaction with redness swellin and warmth to the touch patient went to urgent care and was given an antibiotic and steriod to treat
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 07.10.2023
- Impfdatum
- 02.10.2023
- Beginn
- 02.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
Extra dose of PCV 20 given on 10/02/23. Pt had already recieved a dose in May 2023. And is up to date with PCV vacicne. No complications or symptoms reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypothryoidism GERD
- Andere Medikamente
- None
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 19.09.2023
- Impfdatum
- 15.09.2023
- Beginn
- 15.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
APN advised patient desired vaccines, indicating which vaccines to be given by circling names on vaccine sheet. It was noted patient had Tdap in 2012 and needed TD rather than Tdap. When vaccines were pulled from pharmacy, Tdap and TD both were pulled and given. Patient notified 09/15/2023 of error and denies any adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 16.08.2023
- Impfdatum
- 09.06.2023
- Beginn
- 09.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Immunisation reaction
Symptomtext
Unspecified adverse effect of drug or medicament, initial encounter on 2023-06-09, Unspecified adverse effect of drug or medicament, initial encounter on 2023-06-09, Adverse effect of other vaccines and biological substances, initial encounter on 2023-06-11.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunisation reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Rheumatoid arthritis without rheumatoid factor, unspecified site; Systemic lupus erythematosus NOS; Body mass index [BMI] 37.0-37.9, adult; Other long term (current) drug therapy; Anemia in other chronic diseases classified elsewhere; Thyrotoxicosis with diffuse goiter without thyrotoxic crisis or storm; Vitamin D deficiency, unspecified; Rheumatoid arthritis, unspecified; Encounter for adult health check-up NOS; Encounter for screening for other viral diseases; Encounter for screening mammogram for malignant neoplasm of breast; Need for immunization against single bacterial diseases; Body mass index [BMI] 38.0-38.9, adult; Anemia in other chronic diseases classified elsewhere; Thyrotoxicosis with diffuse goiter without thyrotoxic crisis or storm; Encounter for adult health check-up NOS
- Vorgeschichte
- -
- Andere Medikamente
- ATORVASTATIN CALCIUM 40 MG ORAL TABS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 15.08.2023
- Impfdatum
- 07.06.2023
- Beginn
- 09.06.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Patient was given Prevnar 20, instead of the Boostrix Tdap that was ordered. No reaction or undesired outcomes. Patient was given the correct vaccine on 6/14/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypoxia h/o Pneumonia Nonalcoholic steatohepatitis Hyperprolactinemia (HCC) Hypoparathyroidism (HCC) Pituitary microadenoma (HCC) Postoperative hypothyroidism h/o Otitis externa h/o Mastoiditis Abdominal pain Developmental delay Elevated blood-pressure reading without diagnosis of hypertension Encounter for lipid screening for cardiovascular disease History of amenorrhea History of thyroidectomy Leukocytosis History of thyroid cancer Obesity Pain in both feet Tachycardia Vitamin D deficiency Noncompliance with medication regimen h/o COVID-19
- Andere Medikamente
- Tylenol Cabergoline Ketoconazole Levothyroxine Vitamin E
- Allergien
- Iodine
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 07.08.2023
- Impfdatum
- 07.08.2023
- Beginn
- 07.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Patient was given wrong vaccine. She was to receive a HPV but was given Prevnar20.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyperlipidemia, seasonal allergies
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 04.08.2023
- Impfdatum
- 12.07.2023
- Beginn
- 12.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Pt was given an extra dose of Shingrix unknowingly, they had previously received 2 doses of Shingrix, a few years ago. symptoms or events unknown
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- COPD
- Andere Medikamente
- unknown
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 96,0
- Geschlecht
- F
- Eingang
- 20.07.2023
- Impfdatum
- 18.07.2023
- Beginn
- 18.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
pt was administered vaccine in our office on 6/13/23 and than Pharmacy administered same vaccine on 7/18/23 - no obvious issues with pt but pt is 93yrs old and there is some concern
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- IBUPROFEN IB ORAL
- Allergien
- Aspirin Aspirin Itching, Unknown Not Specified Allergy 6/13/2023 Past Updates Deletion Reason: Metformin Metformin Nausea Only Not Specified Allergy 6/13/2023 Past Updates Deletion Reason: Sulfa (Sulfonamide Antibiotics) Sulfa (Sulfonamide Antibiotics) Not Specified 7/27/2020 Past Updates Unknown Deletion Reason: Amlodipine Amlodipine Rash Low 8/12/2021 Past Updates Generic only Deletion Reason: Atorvastatin Calcium
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 03.07.2023
- Impfdatum
- 26.06.2023
- Beginn
- 26.06.2023
- 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
Symptomtext
pt felt hot, sat and fanned herself. was okay after sitting a few mins
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling hot
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 0,4
- Geschlecht
- F
- Eingang
- 20.06.2023
- Impfdatum
- 20.06.2023
- Beginn
- 20.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Prevnar 20 given to patient when it should of been Prevnar 13. Last dose of Prevnar 13 was 02-21-23
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 16.06.2023
- Impfdatum
- 12.06.2023
- Beginn
- 12.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Fungal infection
Symptomtext
Pt called 4 days later 06/16/23 that she got a yeast infection that afternoon after the vaccine. Spoke with provider on 06/16/23
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fungal infection
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Leg swelling Venous insufficiency Bilateral pulmonary embolism Acute deep vein thrombosis (DVT) of distal vein of left lower extremity COVID-19 virus infection Hypomagnesemia Obesity (BMI 30-39.9) HTN (hypertension) Hyperlipidemia Hypothyroidism Lymphedema Morbid obesity Stage 3 chronic kidney disease On apixaban therapy MGUS (monoclonal gammopathy of unknown significance) Other hemorrhoids Lichen planus Gastro-esophageal reflux disease with esophagitis Constipation Diverticular disease of colon
- Andere Medikamente
- vitamin D3 (CHOLECALCIFEROL) 25 mcg tablet aspirin 81 MG EC tablet hydrALAZINE (APRESOLINE) 50 MG tablet apixaban (ELIQUIS) 5 MG tablet hydrALAZINE (APRESOLINE) 25 MG tablet bumetanide (BUMEX) 1 M
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 10.06.2023
- Impfdatum
- 20.05.2023
- Beginn
- 21.05.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Morphoea
Skin mass
Swelling
Symptomtext
the patient describes large red swelling after the vaccination, which then resolved and left a lump under the skin. On examination, the lump is visible under the skin, and there is a white patch over the lump and red discoloration of the skin. Similar in appearance to morphea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- lisinopril, atenolol, amitriptyline, Flonase sensimist, diclofenac
- Allergien
- latex
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 09.06.2023
- Impfdatum
- 08.06.2023
- Beginn
- 08.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product preparation issue
Symptomtext
Patient was in no harm. Pt was given the liquid suspension only. Pt did NOT receive the lyophilized powder.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Lexapro Protonix Wegovy weight loss injections
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 06.06.2023
- Impfdatum
- 06.06.2023
- Beginn
- 06.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient was not due yet, No adverse reaction seen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Type 2 diabetes Hypertension congestion heart failure
- Andere Medikamente
- Calcium 500 mg Ozempic 1Mg /dose inj Vitamin D3 Clopidogrel 75 mg Lipitor 80 mg Lisinopril 30mg Invokana 100 mg Eliquis 5 mg Carvedilol 6.25 mg tab\ Furosemide 40mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 02.06.2023
- Impfdatum
- 29.05.2023
- Beginn
- 30.05.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint swelling
Peripheral swelling
Symptomtext
Patient reported to the pharmacy that he ad right leg/ankle/foot swelling after the vaccine. He pointed out it was the same side of the body he got his Prevnar 20 injection (right arm).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Joint swelling
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- M
- Eingang
- 02.06.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site cellulitis
Symptomtext
developed cellulitis after receiving the shot of Prevnar 20/information on where the cellulitis was: left arm at the injection site, in the deltoid; This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team. An 86-year-old male patient received pneumococcal 20-val conj vac (dipht CRM197 protein) (PREVNAR 20), as dose number unknown, 0.5ml single (Lot number: GN1898, Expiration Date: Sep2024), in left deltoid for immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing). Concomitant medication(s) included: OMEPRAZOLE; MIDODRINE; POTASSIUM; TAMSULOSIN. The following information was reported: VACCINATION SITE CELLULITIS (intervention required), outcome "unknown", described as "developed cellulitis after receiving the shot of Prevnar 20/information on where the cellulitis was: left arm at the injection site, in the deltoid". Therapeutic measures were taken as a result of vaccination site cellulitis. Additional information: Reporter was wondering if something was wrong with a batch of Prevnar 20 (see lot number below). She has two patients that developed cellulitis after receiving the shot. LOT: GN1898. NDC: 0005 2000 01. Added information on where the cellulitis was for each patient: left arm at the injection site, in the deltoid. Nurse stated, "Our management team had suggested to call as we had 2 patients that actually had developed cellulitis after receiving Prevnar 20. So, my doctor was actually little concerned that there is actually something wrong with the batch because we have given this out numerous times but all of a sudden two patients within a week apart developed cellulitis." The reporter considered "developed cellulitis after receiving the shot of prevnar 20/information on where the cellulitis was: left arm at the injection site, in the deltoid" associated to pneumococcal 20-val conj vac (dipht CRM197 protein).; Sender's Comments: A possibly contributory role of PREVNAR 20 in triggering the onset of vaccination site cellulitis cannot be fully excluded, considering the temporal relationship. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate,Linked Report(s) : US-PFIZER INC-202300204006 Same reporter, drug, event and different patient;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension
- Andere Medikamente
- OMEPRAZOLE; MIDODRINE; POTASSIUM; TAMSULOSIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 31.05.2023
- Impfdatum
- 30.05.2023
- Beginn
- 30.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
No adverse event. Subsequently found out patient received the same Prevnar 20 dose on 5/26/23, we were not informed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- meloxicam
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 31.05.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Symptomtext
developed cellulitis after receiving the shot of Prevnar 20; This is a spontaneous report received from a contactable reporter(s) (Nurse) from medical information team. A patient (no qualifiers provided) received pneumococcal 20-val conj vac (dipht CRM197 protein) (PREVNAR 20), as dose number unknown, single (Lot number: GN1898), in right deltoid for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: CELLULITIS (medically significant), outcome "unknown", described as "developed cellulitis after receiving the shot of Prevnar 20". Clinical course: Caller mentioned that they have two patients who developed cellulitis after receiving the shot of Prevnar 20 and they believe that there is something wrong with the batch; Sender's Comments: Based on the available information in the case, an association between the reported events CELLULITIS and The suspected drug cannot be ruled out. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 26.05.2023
- Impfdatum
- 24.05.2023
- Beginn
- 24.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Product storage error
Symptomtext
Patient recieved vaccine 4 days after expiration date. Patient was here for the allotted time of 15 minutes after and had no reactions. Was not caught that vaccine was expired till entered into epic. Provider notified and Moderna was notified that did a Moderna medical inquiry to find the viability of the vaccine after date of expiration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- Thank you for your patience. Analysis of the vials associated with your storage excursion is complete. The vaccine administered on May 24, 2023 from lot number 051D22A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HYPERLIPIDEMIA Mild, anxiety, and depression
- Andere Medikamente
- acetaminophen (TYLENOL) 325 MG tablet, albuterol 108 (90 Base) MCG/ACT inhaler, alclometasone (ACLOVATE), amphetamine-dextroamphetamine (Adderall) 10 MG tablet, aspirin 81 MG chewable tablet, benzonatate (Tessalon Perles) 100 MG capsule, Ch
- Allergien
- Shellfish Allergy (food Or Med) and Penicillin's
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.05.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Liquid product physical issue
Symptomtext
Caller mentioned she opened a box of Prevnar 20 and she noticed there is a brown small precipitant in the vaccine; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from medical information team and product quality group. A patient (no qualifiers provided) received pneumococcal 20-val conj vac (dipht CRM197 protein) (PREVNAR 20), as dose number unknown, single (Lot number: GN1898) for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: LIQUID PRODUCT PHYSICAL ISSUE (non-serious), outcome "unknown", described as "Caller mentioned she opened a box of Prevnar 20 and she noticed there is a brown small precipitant in the vaccine". Additional information: Caller mentioned she opened a box of Prevnar 20 and she noticed there is a brown small precipitant in the vaccine. She said it is not a lot, but there is a small brown precipitant. She wants to know if this is common.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Liquid product physical issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 15.05.2023
- Impfdatum
- 15.05.2023
- Beginn
- 01.05.2023
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
patient received a second dose of Prevnar 3 months after his first. he told the pharmacy he had received a flu shot in February
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- not applicable
- Aktuelle Erkrankungen
- anxiety
- Vorgeschichte
- diabetes, hyperlipidaemia, hypertension
- Andere Medikamente
- januvia,farxiga,glipizide,lisinopril,rosuvastatin,alprazolam
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 13.05.2023
- Impfdatum
- 05.05.2023
- Beginn
- 05.05.2023
- 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
No adverse event
Symptomtext
It was discovered on 05/13/23 that patient was given a second dose of Prevnar by mistake on 05/05/23. Per The Immunization System, patient has already gotten 1 dose of Prevnar 20 on 10/12/2022. Patient's record from pharmacy dispensing system also confirmed the aforementioned error. Patient was contacted regarding this incident and reported no adverse side effects since his 2nd dose of Prevnar 20.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Doxycylcine hyclate 100 mg Take 1 tablet by mouth Daily Start 2 days prior to travel, continue 1 month after travel
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 09.05.2023
- Impfdatum
- 01.05.2023
- Beginn
- 01.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Symptomtext
Cellulitis upper arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -