- Staat
- IL
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 01.10.2021
- Impfdatum
- 29.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Endotracheal intubation
Haemorrhage
Pulmonary embolism
Symptomtext
Patient admitted 1-2 days following administration of the vaccines to hospital with multiple B/L PEs, Question of saddle embolus, now intubated, had been on pressors, had bleeding and not able to tolerate TPA as result
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Elevated PSA - near 30, HLD, mild DOE over past month and PAD
- Vorgeschichte
- HLD, PAD
- Andere Medikamente
- Pravastatin 10 mg
- Allergien
- Aspirin
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast swelling
Computerised tomogram head
Condition aggravated
Culture urine
Electrocardiogram
Erythema
Full blood count
Hypophagia
Impaired self-care
Injection site erythema
Injection site swelling
Metabolic function test
Myocardial necrosis marker
Peripheral swelling
SARS-CoV-2 test negative
Speech disorder
Urinary tract infection
Urine analysis
Symptomtext
Patient is a Nursing Home Resident and received her vaccines as a Hospital Outpatient. They were given at 10:41 am, at bed time around 8:00 pm staff noticed she was unable to get herself ready for bed. This AM she has redness and swelling in her right arm, shoulder and breast areas, she is not eating or drinking and she rambles in her speech. She was taken to the Clinic and Admitted to the hospital. , Her R arm was put in a sling, ice/heat applied, Xrays taken, a Urine sample obtained and IV Fluids started at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 12-29-21 11:07 am CBC, CMP Urinalysis (sent for culture) 12:06 pm Cardiac Enzymes, COVID Test (Negative), CT of Head 1419 EKG, 1550 Rocephin ! gram IV given for UTI
- Aktuelle Erkrankungen
- UTI, possible UTI now.
- Vorgeschichte
- UTIs, GERD, Dementia, Depression, Hypertension, Hypomagnesemia, Osteoarthritis, Hypothyroidism, Seborrheic Keratosis (imflamed) TIA, Hx R Shoulder pain with possible rotator cuff injury
- Andere Medikamente
- Acetamenophin, AmLODIPine, CeleBREX, Colace, Cranberry Capsule,Donepazil HCL, Esomeprazole Magnesium, HydroCHLOROthiazide, Levothyrozxine, Lisinopril, Multi Vitamin, Namenda, Potassium Chloride, Zoloft, Calcium 600+D3, Lubricant Eye Drops,
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 07.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Condition aggravated
Dysstasia
Malaise
Neurological symptom
Symptomtext
Patient stated after receiving vaccine he left store, walked across the street and felt back pain, neurological symptoms resulting in feeling unable to remain standing. Patient felt light-headed. Ambulance was called to the scene. Patient stated he felt ill for about 10 to 15 minutes. When ambulance arrived they check all vitals and all were within normal range. BP was 150/75 per patient at initial check.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Patient had bronchitis for several months which resolved about a week prior to vaccination.
- Vorgeschichte
- Crohns disease; on and off back pain.
- Andere Medikamente
- Recently completed medrol dosepak but did not take any medications today.
- Allergien
- No allergies to patient
- Vorherige Impfungen
- Patient had mild myocarditis after receiving covid vaccine in April and May.
- Staat
- MA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Erythema
Mobility decreased
Peripheral swelling
Symptomtext
Left arm progressive swelling, erythema, poor mobility, worsening over 2 days, extending to elbow
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hereditary spherocytosis; type II DM
- Andere Medikamente
- -
- Allergien
- Lactose, doxycycline
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 09.10.2021
- Impfdatum
- 06.10.2021
- Beginn
- 09.10.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Axillary pain
Injection site pain
Joint range of motion decreased
Mobility decreased
Pain
Pain in extremity
Symptomtext
Patient received vaccine on 10/06/202 on his right arm for Pneomonia-23 (pneumovax-23). He came in today 10/09/2020 saying that his arm has been sore ever since he received that vaccine alongside a flu vaccine that he received on the same day on the left arm which was slightly sore for that day. He says the whole right shoulder hurts when he tries to move the arm and the upper arm on the injection site is sore to touch tender around the armpit area. The arm has limited range motion. He can barely lift his arm sideways or forward and according to the patient he cannot use the arm to do anything, He says he had a steroid injection on the same arm about 14 days prior to receiving the vaccine. He wanted to know if that was normal and what he could, The patient says he will contact his primary care physician as soon as he can if there is no improvement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetes; chronic pain; HTN
- Andere Medikamente
- glyburide 2.5 mg; metformin 1000 mg; tizanidine 4mg; simvastatin 20mg; tramadol 50 mg; amlodipine 5mg; xarelto 2.5 mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 07.10.2021
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Arthralgia
Injected limb mobility decreased
Injection site pain
Neck pain
Symptomtext
Patient describes as severe pain and loss of mobility in the left arm ranging from the neck/shoulder area down to the elbow. Pain started day of vaccination few hours after administration, and worsened over time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- Per patient, patient has been seen by multiple providers and has multiple ER visits. Treatment was not discussed between us but patient was prescribed medication for the pain
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, Hyperlipidemia
- Andere Medikamente
- Benazepril, atorvastatin, ezitimibe,dyazide
- Allergien
- Codeine derivitives
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 28.09.2021
- Impfdatum
- 25.09.2021
- Beginn
- 25.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Cellulitis
Dizziness
Erythema
Feeling hot
Headache
Hypotension
Nasal congestion
Respiratory tract congestion
Skin warm
Symptomtext
Patient received her Fluzone HD and pneumovax 23 both in her left arm on 9/25/2021. On Saturday 9/25/2021 she reports getting stuffed up. Then Sunday morning patient had a headache, congestion, temp of 103, she felt hot, dizzy, and reports her blood pressure was low 103/57 pulse 111. Sometime Sunday evening she noticed the redness on her arm and her arm was warm. She called her doctor at the advice of a visiting nurse. She had a zoom visit with her doctor. The doctor said it was cellulitis and prescribed cephalexin and prednisone for her to take care of it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- -
- Andere Medikamente
- fluticasone nasal spray, hydrochlorothiazide 25mg, lisinopril 40mg, metformin 500mg, gabapentin 100mg, azelastine nasal spray
- Allergien
- no known
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 23.09.2021
- Impfdatum
- 21.09.2021
- Beginn
- 21.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Diplopia
Disorientation
Fatigue
Joint range of motion decreased
Nausea
Pain in extremity
Tremor
Symptomtext
The same day after the shot the patient experienced disorientation, double vision, shaking. The patient was tired, has a poor apetite, and is nauseous. States these have resolved and she has severe pain and little motion in her right arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- benzonatate, lamotrigine, quetiapine, alprazolam
- Allergien
- celiac disease, latex, yeast, wheat, barley, oats
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 31.07.2022
- Impfdatum
- 30.07.2022
- Beginn
- 30.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Gait disturbance
Symptomtext
patient reported pain in her hips with direct onset at the time of vaccination, trouble walking. called EMS, took her BP which was 207/110 mmHg. Upon their arrival, her BP had come down a bit, and she reported no pain and was able to walk but because of her BP they wanted her to been taken into the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no known
- Vorgeschichte
- osteoarthritis, hypertension, macular degeneration
- Andere Medikamente
- carbidopa-levodopa 25/250 1 tablet twice daily xiidra 1 drop into each eye twice daily xanax 0.5 mg 1 tablet daily metoprolol er 100 1 tablet daily amlodipine 2.5 1 tablet daily spironolactone 25--1/2 tablet daily
- Allergien
- penicillins
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 22.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Injection site extravasation
Product administration error
Symptomtext
I injected the needle into the left muscle and there was some resistance, but I pushed the needle into the muscle as far as I could. The needle was in the muscle, but after depressing the plunger, the vaccine seemed to drip out of the arm. The needle tip stayed secure on the plunger, so I do not think the needle tip was loose, at least from what I could tell. Probably more than half of the dose seemed leaked out onto the patient's arm. I do not know for sure why this happened. This is the first time this has happened to me. This is being reported as an administration event, not as a vaccine adverse event. Patient appeared to be fine, and I did not see anything unusual with his left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site extravasation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known drug or food allergies
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site swelling
Injection site warmth
Local reaction
Symptomtext
Pt stated she started having some swelling in the afternoon after getting the shot. She didn't think much of it until the next day when the swelling got worse, warm to the touch, and had some pain. She was putting ice on it but didn't help much either. When she called on Monday, 3/14/22, it hasn't gotten worse, but the swelling is from below the injection site to the elbow. I consulted her to take benadryl, apply cream if she has, and continue icing it. She will continue to monitor and call back if it worsens. As of now, the reaction was just locally on the arm where she got the injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 17.02.2022
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blister
Infection
Pruritus
Rash
Skin lesion
Symptomtext
Narrative: Patient received both the influenza and pneumococcal-23 vaccines on 10/18/21 at clinic. Patient called PCP on 11/1/21 stating that he developed "small itchy 'blisters' on his chest/back and behind his ears and on his eyelids. He denies an trouble breathing, swallowing or with oral swelling." Patient was advised to take OTC Benadryl and report to the ER or urgent care if more symptoms developed. On 12/10/21, Patient presented to PCP, and his rash was still present. Lesions were infected, and Patient was prescribed Bactrim DS BID, a Medrol Dosepak, and hydroxyzine HCl 25mg.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain in extremity
Peripheral swelling
Symptomtext
PAIN, REDNESS, SWELLING OF LEFT ARM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Erythema
Induration
Pain in extremity
Peripheral swelling
Symptomtext
PAIN, REDNESS, INDURATION, AND SWELLING OF LEFT ARM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- LATEX CIPROFLOXACIN AUGMENTIN
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Malaise
Pain in extremity
Peripheral swelling
Pyrexia
Rash
Symptomtext
Patient complained of feeling unwell the next morning (weak and fever of 103 F which lasted for 4 days) and started feeling pain in her arm. During the next day her arm had some swelling and on the 3rd day a rash that surrounded her bicep formed. It is now 2 weeks later and she has mild soreness and the rash is still present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- She went to urgent care and was given an antibiotic.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 1,0
- 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
Skin warm
Symptomtext
The patient reported on 11/11/21 they received Pneumovax 23 on 11/5/21 and on 11/6/21 experienced painful, red & hot to touch, swollen, itching left arm for 2 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- DIABETES
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 08.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash macular
Symptomtext
Patient reported itchy red blotches forming on the administration arm within 24 hours of administration. She reports that it has improved since first appearing, so I advised she take Benadryl and seek medical care if it does not continue to improve.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HTN, anxiety, GERD
- Andere Medikamente
- Nifedipine, estradiol, alprazolam, omeprazole, sertraline
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 12.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Discomfort
Immediate post-injection reaction
Injection site pain
Insomnia
Joint dislocation
Joint laxity
Loss of personal independence in daily activities
Myalgia
Pain
Pain in extremity
Symptomtext
Patient is a 29 year old female patient of Dr. presenting to the office today c/o left arm/shoulder pain x3 weeks. She reports that the pain began immediately while receiving the Flu vaccine in office on 10/12/21. She states that she received the Pneumonia vaccine in the same arm on the same day, which was not painful for her. The Pneumonia shot was given in the lower deltoid and the flu shot was given at the upper deltoid. Patient reports feeling acute pain at the site of injection as the vaccine was being administered. She states that the pain has been constant, has not improved, and is getting worse. It is especially uncomfortable with movement and ADLs, such as: driving, getting dressed, showering, etc. She reports a history of shoulder joint laxity and dislocations in childhood (pt unsure of which shoulder), but states neither shoulder has fully dislocated since middle school when she was playing soccer. She reports that she had extensive PT to both shoulders following the dislocation. She denies experiencing a pain like this in the past, and has not had a similar reaction with previous vaccines. She endorses increased pain with movement and rates it as a 6/10 today. With rest, it is manageable at a 1/10. She denies any bruising, rash, swelling, or pruritis to the injection site/left shoulder. She describes the pain as muscle aches and burning to her left shoulder joint and left arm. She states that it is rare, but occasionally the pain will radiate down to her left wrist. She denies any numbness or tingling in her upper extremities. She denies any recent heavy lifting, strenuous exercise, or falls/trauma. She moved roughly 1 week ago, but states that her mom did the heavy lifting for her d/t discomfort. For pain management, she has been taking 2-3 Advil 200 mg while at work. She states that it helps alleviate some of the pain, but it never completely resolves, just feels more "dull". Patient reports an increase in difficulty sleeping compared to her baseline d/t the pain when she rolls over onto the left side. Of note, she does have a history of narcolepsy, and states that sleep has always been a little tough for her.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Xray pending.
- Aktuelle Erkrankungen
- unk.
- Vorgeschichte
- S/p breast biopsy/ benign phyllodes tumor and atypical ductal hyperplastia; Presented 12/2020 with breast lump; Yearly MRIs recommended; Sleep medicine- narcolepsy with cataplexy; Still trying ot get PA for modafinil, PA in chart on 4/5; Blood pressure; BP Readings from Last 3 Encounters: 10/12/21 126/84; 04/13/21 144/77; 02/24/21 105/66; On beta blocker; BP excellent since starting, despite high stress medical encounter; Asthma PCOS
- Andere Medikamente
- modafinil, ibuprofen, benzaclin gel, atenolol, ascorbic acid.
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 20.10.2021
- Impfdatum
- 15.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Erythema
Fatigue
Headache
Nausea
Pain
Pyrexia
Skin warm
Symptomtext
Pt described nausea, exhaustion, headache, fever, and dizziness starting at 5pm after receiving the vaccinations at 12 pm. She was unable to eat or drink anything for 18 hours. She was able to keep solid food down 2 days after vaccinations at which time she noticed a very large red area that was hot to the touch and painful. She started taking antihistamines and the redness and heat went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- thyroid, cold sores
- Andere Medikamente
- levothyroxine
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 13.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Injection site warmth
Pain
Pain in extremity
Symptomtext
The day following vaccination the patient experienced typical arm soreness but this was accompanied with a large area of swelling, redness, and warmth around the injection site. Patient also had some body aches which have since resolved. The patient presented to the pharmacy 4 days following vaccination to report the reaction and show the pharmacist. Pharmacist visually examined the arm and observed the swelling and redness. Patient confirmed that these symptoms have been improving. Advised the patient to ice the area and to take an OTC anti-inflammatory if appropriate. Patient will call her doctor if the area worsens or does not improve over the next couple of days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- Impfdatum
- 04.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site warmth
Symptomtext
Pt stated she had a red, hot area underneath the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- cellulits on leg
- Vorgeschichte
- -
- Andere Medikamente
- azithromycin, metoprolol er, spironolactone, simvastatin
- Allergien
- KNDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 04.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site erythema
Injection site swelling
Injection site warmth
Symptomtext
pt stated redness, swelling (slight) and warmth around the injection site with around a 3 inch diameter;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 03.10.2021
- Impfdatum
- 30.09.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Injection site erythema
Pain in extremity
Pyrexia
Symptomtext
THE NEXT DAY POST ADMINISTRATION PATIENT FELT THE ARM WAS VERY SORE TO THE PAIN SHE HAD TO TAKE A LOT OF TYLENOL. SHE WAS ALSO TIRED AND HAD LOW GRADE FEVER. AS OF 10/03/21 SHE SAID SHE ALSO HAD REDNESS AROUND THE INJECTION SITE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 01.02.2023
- Impfdatum
- 09.01.2023
- Beginn
- 09.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
No additional AEs or PQC reported; Caller reported expired dose of PNEUMOVAX 23 was administered; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions, concomitant therapies, drug reactions and allergies were not reported. On 09-JAN-2023, the patient was vaccinated with an expired dose of Pneumococcal Vaccine, Polyvalent (23-valent)(PNEUMOVAX23) injection, 0.5 ml, at left (L) deltoid, lot# U003306, expiration date 15-OCT-2022, (strength, dose # and route of vaccination were not provided) for prophylaxis (expired product administered). No additional adverse events (AEs) was reported (no adverse event)
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
- 23.12.2022
- Impfdatum
- 19.12.2020
- Beginn
- 19.12.2022
- Tage bis Beginn
- 730,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
No additional AE details were provided and no additional AE's were reported; the patient was administered PNEUMOVAX 23 after its labeled expiry date; This spontaneous report was received from a pharmacy thechnician and refers to a patient of unknown age and gender. No information on patient's pertinent medical history, concurrent conditions, drug reaction or allergies, and concomitant therapies were reported. On 19-DEC-2020, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, 0.5 milliliter, lot #U003306, expiration date: 15-OCT-2022, administered intramuscularly (anatomical location was not provided) for prophylaxis, after its labeled expiry date (Expired product administered). No additional adverse event (AE) details were provided and no additional AE's were reported (No adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.12.2022
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No additional AE.; An expired dose of PNEUMOVAX 23 was administered to a patient.; This spontaneous report was received from a pharmacist regarding a patient of an unknown age and gender. The patient's medical history, concurrent conditions, and concomitant therapies were not reported. On 12-DEC-2022, the patient was vaccinated with an expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) use as directed to prevent pneumococcal infection, product quantity 1, lot #U003306, expiration date: 15-OCT-2022, (strength, anatomical location, and route of administration were not provided) administered as prophylaxis (Expired product administered). No adverse events were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- U
- Eingang
- 09.11.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No additional AE reported. No PQC reported; HCP reports patient was accidently administered an expired dose of PNEUMOVAX 23 on Oct 21, 2022; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions, and concomitant therapies were not reported. On 21-OCT-2022, the patient was inadvertently vaccinated with an expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) pre-filled syringe, lot #U003306, expiration date: 15-OCT-2022 (strength, anatomical location, and route of administration were not provided) as prophylaxis. No adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 09.11.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No additional adverse event reported; Patient was accidently administered an expired dose of PNEUMOVAX 23; This spontaneous report was received from a registered nurse and refers to a 10-year-old female patient. The patient's medical history included leukaemia with bone marrow transplant in approximately March 2021(also reported as approximately 20 months ago). The patient's concurrent conditions and drug reactions or allergies were not reported. On 24-OCT-2022, accidentally the patient was vaccinated with an expired dose of pneumococcal vaccine, polyvalent (23-valent)(PNEUMOVAX23), lot # U003306, expiration date 15-OCT-2022, in the right deltoid for prophylaxis (dose and route were not reported) (expired product administered). The product had no prior temperature excursions. No additional adverse event and no product quality complain were reported. Concomitant therapies included ketoconazole and colecalciferol (CHOLECALCIFEROL).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Bone marrow transplant; Leukaemia
- Andere Medikamente
- CHOLECALCIFEROL; KETOCONAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.11.2022
- Impfdatum
- 03.11.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No additional AE information provided; PNEUMOVAX 23 vaccine was accidentally administered to a patient after the expiration date; This spontaneous report was received from a medical assistant and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 03-NOV-2022, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) syringe, injection, 0.5 ml, lot number U003306, expiration date: 15-OCT-2022, administered for prophylaxis (strength, and route of administration were not provided) (expired product administered). It was reported that the vaccine was stored appropriately and did not have any temperature excursions. No additional adverse event information was provided (no adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.11.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- 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
No adverse event
Symptomtext
no additional AE reported; expired dose of PNEUMOVAX 23 was administered to the patient on 21OCT2022; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies details were not reported. On 21-OCT-2022, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, 0.5 ml, lot #U003306, expiration date: 15-OCT-2022, administered for prophylaxis (strength, and route of administration were not provided) (Expired product administered). It was reported that the vaccine did not experience a temperature excursion. No additional information provided. No additional adverse event was reported. No product quality complaint was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.11.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
no additional AE reported; expired dose of PNEUMOVAX 23 was administered to the patient on 21OCT2022; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies details were not reported. On 21-OCT-2022, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, 0.5 ml, lot #U003306, expiration date: 15-OCT-2022, administered for prophylaxis (strength, and route of administration were not provided) (Expired product administered). It was reported that the vaccine did not experience a temperature excursion. No additional information provided. No additional adverse event was reported. No product quality complaint was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- -
- Geschlecht
- U
- Eingang
- 28.10.2022
- Impfdatum
- 25.10.2022
- Beginn
- 25.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No additional AE; Nurse calling to report that a dose of PNEUMOVAX23(pfs) with a labeled expiry of 10/15/2022 was administered to a patient on 10/25/2022.; This spontaneous report has been received from a nurse and refers to a patient of an unknown age and gender. The patient's medical history, concurrent conditions, previous drug reactions or allergies, and concomitant therapies were not reported. On 25-OCT-2022, the patient was vaccinated with a labeled expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, at a dose of 0.5 milliliter (ml) (strength, route of administration and vaccination scheme frequency were not provided; lot number U003306 that was verified to be a valid lot number with an expiration date reported as and established as 15-OCT-2022) (expired product administered) for prophylaxis. By the reporting time, the caller confirmed that she was not know if a temperature excursion was involved. No additional adverse event (AE) was reported (no adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 25.10.2022
- Beginn
- 25.10.2022
- 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
Symptomtext
Team member accidentally administered an expired Pneumovax 23 vaccine to patient. Vaccine expired on 10/15/2022. Vaccine was administered on 10/25/2022. Provider, clinical supervisor, nurse lead (reporter), and patient were notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
vaccine administered 10/24/22 expired 10/15/22, notified provider, will reach out to oncologist to determine need to revaccinate
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- leukemia
- Vorgeschichte
- leukemia
- Andere Medikamente
- ciprodex, cholecacliferol
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 24.09.2022
- Impfdatum
- 20.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
No additional AE reported; HCP reported PNEUMOVAX 23 was administered after a temperature excursion to a patient.; This spontaneous report has been received from a medical assistant (healthcare professional (HCP)) regarding a patient of unknown age and gender. The patient's concomitant medications, pertinent medical history, and drug reactions/ allergies were not reported. On 20-JUL-2022, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, lot #U003306, expiration date: 15-OCT-2022, administered once for prophylaxis (strength, dose, route of administration and anatomical location were not provided) after temperature excursion of 62 Fahrenheit (F) for 5 hours 12 minutes on 12-APR-2022 (product storage error). There was no previous temperature excursion. There was no additional adverse event (AE) reported, and no further information was provided. This is one of four reports received from the same reporter. ; Sender's Comments: US-009507513-2208USA010789: US-009507513-2209USA000715: US-009507513-2208USA010861:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 24.09.2022
- Impfdatum
- 06.07.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
No additional AE reported; HCP reported PNEUMOVAX 23 (PFS) was administered after a temperature excursion to a patient.; This spontaneous report has been received from a medical assistant (healthcare professional (HCP)) regarding a patient of unknown age and gender. The patient's concomitant medications, pertinent medical history, and drug reactions/ allergies were not reported. On 06-JUL-2022, the patient was vaccinated with an improperly stored dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, lot #U003306, expiration date: 15-OCT-2022, administered once for prophylaxis (dose, route of administration and anatomical location were not provided) after temperature excursion of 62 Fahrenheit (F) for 5 hours 12 minutes (which occurred on 12-APR-2022) (product storage error). There was no previous temperature excursion. There was no additional adverse event (AE) reported, and no further information was provided. This is one of four reports received from the same reporter. ; Sender's Comments: US-009507513-2208USA010789: US-009507513-2208USA010861: US-009507513-2209USA000730:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 21.09.2022
- Impfdatum
- 14.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
No additional AE reported.; HCP reported PNEUMOVAX 23 (PFS) was administered after a temperature excursion to a patient.; This spontaneous report was received from a medical assistant referring to a patient of unknown age and gender. The patient's concurrent conditions, medical history, drug reactions/allergies and concomitant therapies were not reported. On 14-JUN-2022, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) once (strength, dose and route of administration were not provided), lot #U003306, expiration date: 15-OCT-2022, administered for prophylaxis, after a temperature excursion (Product storage error) occurred on 12-APR-2022 in 62 degrees Fahrenheit for 5 hours 12 minutes. No previous temperature excursion. No additional adverse event (AE) reported. This is one of four reports received from the same reporter. ; Sender's Comments: US-009507513-2208USA010861: US-009507513-2209USA000715: US-009507513-2209USA000730:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.09.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
no adverse event; administered after a temperature excursion; This spontaneous report was received from a medical assistant referring to a patient of unknown age and gender. No information about the patient's pertinent medical history, concurrent conditions, concomitant medications, or drug reactions or allergies was provided. On 27-APR-2022, the patient started therapy with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX 23) once for prophylaxis (lot# U003306, expiry date 15-OCT-2022, strength, route of administration, vaccination scheme frequency, anatomical location, and dose were not reported) after a temperature excursion (occurred on 12-APR-2022, temperature: 62 Fahrenheit (F); time frame: 5 hours 12 minutes) (product storage error). There was no previous temperature excursion. No additional adverse event was reported (no adverse event). This was one of four cases from the same reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 28.07.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
No additional AE reported; patient was scheduled to receive GARDASIL 9 but was accidentally administered a dose of PNEUMOVAX 23 instead; This spontaneous report was received from a registered nurse concerning a patient of unknown age (reported as "under the age of 50 years") and gender. The patient's medical history, concurrent conditions, and concomitant medication were not provided. On 17-FEB-2022, the patient was inadvertently administered a dose of Pneumococcal Vaccine, Polyvalent (23-valent) (PNEUMOVAX23) 0.5 ml, lot #U003306, expiration date 15-OCT-2022, for prophylaxis instead of HPV rL1 6 11 16 18 31 33 45 52 58 VLP vaccine (yeast) (GARDASIL 9) (Wrong product administered) (Route of administration, and injection anatomical location were not provided). No additional adverse events were reported (No adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 0,2
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Vaccine is labeled for use in patients 2 years and older. Patient is 2 months old. Failed to read packaging appropriately.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 17.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
No adverse event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- No test needed
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetes, HIV/Aids
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Medication error
No adverse event
Symptomtext
Med error. No adverse event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 26.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Fall
Muscular weakness
Symptomtext
Patient stated that their legs fell out from under them the morning after receiving all four vaccines. Patient denies loosing consciousness or any symptoms of syncope or loosing consciousness. Patient was brought to the ER and was kept in the hospital for a three day stay. Stated that she the hospital was not able to determine the cause of her fall.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fall
- Hospital-Tage
- 3,0
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Patient denies any illness at time of vaccination.
- Vorgeschichte
- Type 2 diabetes
- Andere Medikamente
- Patient stated they do not take any OTC medications. Unknown prescription medication history.
- Allergien
- No known allergies.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Extra dose administered
Symptomtext
Patient received Fluad and PPSV-23 in the left arm and was diagnosed with cellulitis of the left arm soon after.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- -
- Geschlecht
- M
- Eingang
- 21.10.2021
- Impfdatum
- 28.09.2021
- Beginn
- 28.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Skin laceration
Syringe issue
Symptomtext
Cut his finger requiring a bandaid; One of the two finger flanges broke off; This spontaneous report was received from a Licensed Practical Nurse, refers to a male patient, who was a physician of unknown age. Information regrading the patient's pertinent medical history, concurrent conditions, known allergies and concomitant therapies was not provided. On 28-SEP-2021, the physician administered pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23), with lot # U003306 has been verified to be a valid lot number and expiration date on 15-OCT-2022 to a patient (captured in MARRS # 2109USA007035) for prophylaxis. While administration, one of the two finger flanges of the vaccine broke off (syringe issue), which caused a cut on his finger requiring a band aid (skin laceration). The vaccine was administered to the patient. The physician disposed pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) syringe into sharp container. Product was not able to be retrieved. At the time of the report, the outcome of skin laceration was unknown. Causality between the event skin laceration and vaccination with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) was not provided. This is one of two cases received by the same reporter. ; Sender's Comments: US-009507513-2109USA007035:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Skin laceration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- -
- Geschlecht
- M
- Eingang
- 21.10.2021
- Impfdatum
- 28.09.2021
- Beginn
- 28.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Syringe issue
Symptomtext
One of the two finger flanges broke off; The vaccine was still administered to the patient as the finger flnage breaking off was the only defect.; This spontaneous report was received from a Licensed Practical Nurse, referring to a 76 year old male patient. Information regarding the patient's pertinent medical history, concurrent conditions and concomitant therapies was not provided. The patient had no known allergies. On 28-SEP-2021, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23), with lot # U003306 has been verified to be a valid lot number and expiration date, on a dose of 0.5 milliliter, by intramuscular route in the right arm, as it was age appropriate. It was reported that, on the same date, while the physician was administering pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23), one of the two finger flakes broke off (syringe issue and poor quality product administered). It was reported that the physician, cut his finger and it required a band aid (captured in MARRS # 2110USA004833). It was also reported that, the vaccine was still administered and that the patient did not even know what happened. The vaccine was not able to be retrieved as the physician disposed the pieces into sharp container. This is one of two cases received by the same reporter. ; Sender's Comments: US-009507513-2110USA004833:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 15.10.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Tenderness
Symptomtext
The day after her immunizations, the patient reports to me a swollen upper arm and sensitive to touch. She denies other symptoms at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Peripheral swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 12.10.2021
- Impfdatum
- 09.10.2021
- Beginn
- 10.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Skin irritation
Skin warm
Symptomtext
SYMPTOMS - LOCAL IRRITATION , REDNESS, HOTNESS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- BACTRIM DS 1TAB BID
- Aktuelle Erkrankungen
- NOTHING
- Vorgeschichte
- NOTHING
- Andere Medikamente
- ADDERALL XR 30 MG
- Allergien
- NO ALLERGIES
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 09.10.2021
- Impfdatum
- 07.10.2021
- Beginn
- 09.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Symptomtext
Cellulitis in left anterior upper arm, looked to be about 2" x 3" in size.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Shellfish, Sulfa anbitiotics
- Vorherige Impfungen
- -