- Staat
- VA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 28.07.2022
- Impfdatum
- 28.07.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Dizziness
Dyspnoea
Feeling hot
Flushing
Symptomtext
HOT FLUSHING OF FACE, STOMACH PAIN, LIGHT HEADEDNESS, SHORTNESS OF BREATH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- COCHLEAR IMPLANT
- Vorgeschichte
- HIGH BLOOD PRESSURE, ACID REFLUX
- Andere Medikamente
- PREDNISONE, TRELEGY ELLIPTA, VITAMIN D2 50,000U, PRIMIDONE, MONTELUKAST, HYDROXYCHLOROQUINE, ESOMEPRAZOLE, OXCARBAZEPINE, AND LOSARTAN.
- Allergien
- VALPROIC ACID, HYDANTOINS
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Induration
Mobility decreased
Peripheral swelling
Skin warm
Symptomtext
Pt's arm got swollen, hot to touch, and had hardened tissue. It was also difficult to lift her arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Pt rec'd antibiotic shot at the Urgent Care. 7/20/22, antibiotic Cephalexin 500mg was started orally 7/21/22 Arm was not improving so pt went to the ER where care was given.
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- hypertension
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Pain in extremity
Paraesthesia
Symptomtext
Pt received 2 IMZ's on the left arm 1 inch apart on 11/29/21. Pt started to feel the pain, numbness and tingling on the left arm that radiated to the left shoulder. On 2/21/22 when pt came back for second dose of Shingrix and reported that the numbness travel down the the elbow/mid arm area overtime. Now the numbness is by the fingers only.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- not known
- Vorgeschichte
- none
- Andere Medikamente
- not known
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Injection site pain
Injection site swelling
Symptomtext
65yr old patient presented on 1/4/22 for well visit. Patient was ordered Pneumococcal polysaccharide vaccine 23-valent greater than or equal to 2yo SQ/IM (PNEUMOVAX-23) to be administered during visit. RN administered Pneumococcal Polysaccharide 23-Valent (Pneumovax-23) LOT # U010533 IM in patient's left deltoid. On 1/5, patient contacted office to report should pain and swelling near injection site. Patient indicated limited range of motion. Patient endorsed taking acetaminophen without improvement. Patient felt may have "bursitis" and needs steroid injection. Patient scheduled ortho sports medicine appointment (1/11/22) however, later canceled as symptoms improved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Injection site erythema
Injection site pain
Injection site paraesthesia
Symptomtext
Patient described redness and pain along with tingling starting from injection site, which then spread down to elbow and shoulder blade. It initially started at about 8PM on the day of vaccination and then continued, reported after 2 days and was still present. Patient tried taking both benadryl 25 mg and naproxen 220 mg neither provided relief from burning or pain. Informed patient to continue trying benadryl as tolerated and tylenol or ibuprofen for pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypersensitivity
Injected limb mobility decreased
Injection site pain
Product administered at inappropriate site
Symptomtext
Patient received pneumovax 23 vaccine on 12/7/21. Patient called pharmacy on 12/9/21 and stated she began feeling pain at injection site shortly after vaccine adminstration and went to emergency room later that night due to extreme pain. Patient stated the emegency room physican told her she was not having an allergic reaction and the pain was due to vaccine administration too high in the arm. Patient said she was given pain medication at the emergency room but is still having pain and cannot move her arm 2 days later. Patient will follow up with primary care physician if pain continues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- Emergency room visit 12/7/21
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 28.11.2021
- Beginn
- 28.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extensive swelling of vaccinated limb
Injection site erythema
Injection site swelling
Mobility decreased
Nausea
Pain in extremity
Pyrexia
Symptomtext
Extreme swelling, redness of entire deltoid and bicep area to 1/2" above elbow of left arm; Nausea; Fever (100-104.1); Loss of motion; Excessive pain over entire bicep area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Primary Immune Deficiency; Hashimoto; ITP; Psoriasis / Psoriatic Arthritis
- Andere Medikamente
- Adderall 10 mg OD; Levothyroxine .125 mg OD; Eliquis 5mg BID; Hizentra 10g/50 ml vial - 100ml once weekly
- Allergien
- -
- Vorherige Impfungen
- Tetanus - 2 years old, Unknown brand
- Staat
- WA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 25.10.2021
- 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
Arthralgia
Bursitis
Injected limb mobility decreased
Injection site pain
Ultrasound joint
X-ray abnormal
Symptomtext
The next day (10/13/21) reported significant left upper arm/shoulder pain, limited range of motion. Seen in clinic 10/15/21, supportive care advised over next few days. Due to persistence, imaging obtained. Xray 10/19/21 without bony abnormalities. Ultrasound 10/20/21 showed "IMPRESSION: Left shoulder fluid collection suspicious for bursitis. No evidence of hemorrhage or infection at this time." Referred to physical therapy and steroid taper prescribed(10/22/21).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- See above, treatment for this condition is ongoing and being assessed regularly
- Aktuelle Erkrankungen
- Had left hip intertrochanteric femur fracture s/p surgical repair in early 3/2021.
- Vorgeschichte
- Osteoporosis, hypothyroidism, protein calorie malnutrition (BMI 17.6), depression, peripheral vascular disease
- Andere Medikamente
- Spironolactone, rosuvastatin, potassium, levothyroxine, minocycline, fluocinonide, co Q10, multivitamin, B complex vitamin, calcium carbonate-vitamin D, magnesium, aspirin, denosumab, bimatoprost, timolol
- Allergien
- atorvastatin, alendronate, brimonidine, hydrochlorothiazide, mirtazapine, simvastatin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- Impfdatum
- 09.10.2021
- Beginn
- 10.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Peripheral swelling
Symptomtext
Patient has swelling in the arm, and a tingling sensation down her arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Tramadol
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 04.08.2022
- Impfdatum
- 03.08.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site erythema
Injection site swelling
Symptomtext
pt called and reported swelling at the injection site and redness that spread down to the elbow
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 17.07.2022
- Beginn
- 18.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint range of motion decreased
Pain
Symptomtext
Patient states that she is having painful ROM moving her arm away from her body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- Hypothyroidism, SVT
- Andere Medikamente
- -
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 09.05.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site erythema
Vaccination site pain
Vaccination site warmth
Symptomtext
Localized vaccine reaction (localized redness, warmth, pain)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seizure disorder, migraines, hyperlipidemia, hypertension, allergic rhinitis, osteoporosis
- Andere Medikamente
- Aspirin, vitamin D, vitamin B12, Depakote, ezetimibe, Allegra, Flonase, Boniva, lisinopril, magnesium oxide, Fish oil, Dilantin, Vitamin C
- Allergien
- Mucinex (rash); Pravastatin (rash).
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 02.05.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Gait disturbance
Immediate post-injection reaction
Nightmare
Pain in extremity
Restlessness
Somnolence
Symptomtext
Patient's right arm was immediately very sore (Pneumovax 23). He stated that night he was very restless and had constant nightmares. He woke up shivering, had trouble walking, unsteady and dizzy. His wife prevented a near fall from the dizziness when he was getting up. He stated today 5/5/2022 he is still a bit groggy and unsteady, but is feeling much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Essential tremor, heart disease
- Vorgeschichte
- Cancer, COPD, essential tremor, heart disease
- Andere Medikamente
- Tamsulosin, Oxybutynin, Duoneb, Furosemide, Pregabalin, Pantoprazole, Clopidogrel, Metoprolol, Atorvastatin, Zolpidem, Advair, Alprazolam, Colchicine
- Allergien
- Gabapentin
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 22.10.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 12,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anal sphincter atony
Back pain
CSF protein increased
Gait inability
Hypoaesthesia
Injection site pain
Intervertebral disc disorder
Lumbar puncture abnormal
Magnetic resonance imaging spinal normal
Muscular weakness
Sensory loss
Urinary incontinence
Symptomtext
patient states she had arm pain at the site of injection that worsened throughout the week. went to ED on 11/3/2022 for back pain and bilateral leg weakness and numbness to the point of not being able to walk that started the day before. had associated loss of bladder control. in the ED pt had decreased anal sphincter tone and saddle anesthesia and was admitted to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- 17,0
- Labordaten
- mri on 11/3/2021 showed stable lumbar disc disease lumbar puncture on 11/4/2021 showed high protein
- Aktuelle Erkrankungen
- none that was reported
- Vorgeschichte
- HTN, HLD, Temporal Arteritis, osteopenia,
- Andere Medikamente
- -
- Allergien
- Penicillins and Sulfa
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 31.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Erythema
Injection site erythema
Symptomtext
Redness around area of injection that went from site of injection down to elbow
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Headache
Injection site cellulitis
Pain in extremity
Pyrexia
Symptomtext
24 hours after administration of administration of TDAP and pneumovax, patient developed fever, headache, and right arm pain. Seen 1/28 and diagnosed with cellulitis to right arm at administration site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- No tests ran, clinical diagnosis
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic Small Cell Lymphoma Hypothyroid
- Andere Medikamente
- Levothyroxine
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site swelling
Symptomtext
PATIENT STATED HER ARM STARTED SWEELING FROM INJECTION SITE TO ELBOW. PATIENT WAS IN CONTACT WITH PHYSCIAN AS WELL AND WAS PUT ON 2 ANTIBIOTICS PER PATIENT AND WAS TOLD TO MONITOR AND BE SEEN IF SWEELING DID NOT RESOLVE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- GIVING PRESCRIPTION ANTIBIOTICS (2) PER PATIENT AND WAS TOLD TO BE SEEN IF SWEELING DID NOT RESOLVE.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site cellulitis
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
patient received flucelvax and pneumovax administered in the Left deltoid) around 1-2 pm and started to develop swelling, redness and pain in the left arm extending from underarm to the elbow. The swelling got bigger and redder overnight but started to resolve gradually the next day and following day. She walked into the pharmacy on 12/2/21 and expressed concern about the swelling which is still red and swollen but mildly. She was advised to consult with an MD due to symptoms looking similar to cellulitis. patient consulted with her PCP who diagnosed her with cellulitis and prescribed her Cephalexin and advised to use Ibuprofen and heat pads to resolve the swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetes, hypertension, heart burn,
- Andere Medikamente
- glipizide er 5 mg, pantoprazole 40 mg, triamcinolone 0.1% cream, lisinopril/hydrochlorthiazide 20/12.5 , flonase nasal spray
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 14.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Pain in extremity
Sleep disorder
Symptomtext
The night the vaccine was administered (11/04/21) her bicep muscle and deltoid muscle hurt. She was unable to sleep due to the pain. The bicep pain is reoccurring and still felt today (11/14/21). The next day(11/05/21) the side of the deltoid muscle began to hurt and the deltoid muscle continued to hurt. However these two pain sites, the side of the deltoid muscle and the deltoid muscle pain resolved over time. The patient is still currently feeling pain and strain in her bicep muscle of the right arm. Advised patient to seek medical attention with her provider in which she has not sought out yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 04.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
The patient came in around 11:30 am for vaccine administration of flu and pneumonia. The pneumonia was administered intramuscularly in the left deltoid. The patient was wearing a shirt he bunched up with his other hand and held up for vaccine adminstration. He returned at 7:15 pm to show that under the vaccine adminstration site on the left deltoid his arm was swollen and red. I recommended he ice the area and offered to contact his primary care physician in the morning to let the Dr know of his reaction to the vaccine. I informed the patient that his reaction would be reported to vaers.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash macular
Symptomtext
Pt called 11/4 to state she had 2 spots on arm that received pneumovax 2 days ago. 1 is good sized (3 in a row) and 1 smaller. RPh advised watch and wait as we are just 2 days out. Shared that pt can use cold compress as well as otc pain meds. If area increases in size, streaks, etc. please call back so we can further investigate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash macular
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Administration site swelling
Administration site warmth
Blood culture negative
Hypoaesthesia
Injection site erythema
Injection site mass
Injection site pain
Pain
Pyrexia
Symptomtext
The evening of the vaccine patient's arm got very red, hot, and swollen just below administration site. The next morning the swelling was very pronounce all the way down to the elbow and she was in excrutiating pain and her fingers were numb. We advised her to go to urgent care. They gave her IV dose of antibiotic and a prescription for cephalexin. Patient took 4 doses of cephalexin but swelling, redness got worse and she developed a fever. She went to hospital ER and was admitted. Was given IV antibiotics for 3 days and discharged on Augmentin. Still a lump in arm with some redness, but not near as bad, swelling and arm is warm to touch and still a little sore.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- 3,0
- Labordaten
- On 10/30/21 blood cultures were performed but were negative so no sepsis.
- Aktuelle Erkrankungen
- None,
- Vorgeschichte
- None
- Andere Medikamente
- None........had a flu shot the week prior in same arm
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 23.10.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site discolouration
Injection site rash
Injection site swelling
Rash erythematous
Symptomtext
Patient called having swelling, red rash down to her elbow and blue discoloration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discolouration
- Hospital-Tage
- -
- Labordaten
- Referred her to pcp, er, or urgent care
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- hypertension, peptic ulcer disease
- Andere Medikamente
- Toprol XL 100mg, benaz/hctz 20/25 mg, kcl 10 meq, trazodone 50 mg, protonix 40 mg, simvastatin 40 mg, Eliquis 5 mg
- Allergien
- Sulfa, Pennicillin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- F
- Eingang
- 18.10.2021
- Impfdatum
- 01.09.2020
- Beginn
- 01.10.2021
- Tage bis Beginn
- 395,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Incorrect dose administered
Pain in extremity
Peripheral swelling
Symptomtext
her arm started to hurt and swell up; her arm started to hurt and swell up/ it looks like a bum wound that extends all the way to her elbow; accidently received the vaccine again; the injection site was swollen and red with bumps; redness with her arm; the injection site was swollen and red with bumps; the injection site was swollen and red with bumps; This spontaneous report was received from a pharmacist and a 63 years old female patient referring to the patient herself. Concomitant therapies included blood pressure medication, lifitegrast (XIIDRA) and covid-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE). The patient had seasonal allergies. Information about medical history was not provided. On an unknown date in September 2020 (also reported as about a year ago), the patient was initially vaccinated with the first dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) (anatomical location: right arm, route reported as injection; strength, dose, lot# and expiration date were not reported) for prophylaxis, with no adverse effects to report. On 05-OCT-2021, the patient was accidently vaccinated with the second dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) (0.5 ml, anatomical location: right arm, route reported as injection, lot # U010533, expiration date 29-OCT-2022; strength and frequency were not reported) for prophylaxis again despite not needing the revaccination (incorrect dose administered), a few hours after she received the second dose that her arm started to hurt and swell up. The patient mentioned that over the next few days she was having lots of pain, swelling, and redness with her arm. She mentioned that it was swollen by an inch thick, almost goes 3 quarters around the circumference of her arm, and had a distinct line around it. She mentioned it looked like a bum wound that extended all the way to her elbow. The patient did not seek medical attention but received paracetamol (TYLENOL) and paracetamol (ADVIL) as treatment. The outcome of all events except the event of incorrect dose administered was not resolved. The causality between all events except the event of incorrect dose administered and pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Seasonal allergy
- Vorgeschichte
- -
- Andere Medikamente
- XIIDRA; MODERNA COVID-19 VACCINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 15.10.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Patient she has swelling and redness down the right arm to her elbow. Patient states the arm is warm to the touch and itching. Patient will take benadryl and speak with doctor if symptoms worsen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 12.10.2021
- Impfdatum
- 11.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Symptomtext
Pt got redness at the site of injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 12.10.2021
- Impfdatum
- 07.10.2021
- Beginn
- 08.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Injection site cellulitis
Pain
Pyrexia
Symptomtext
Cellulitis, fever, body aches- admitted to Health center 10/9 or 10/10. getting IV antibiotics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site cellulitis
- Hospital-Tage
- -
- Labordaten
- Admission to hospital r/t cellulitis at injection site
- Aktuelle Erkrankungen
- constipation
- Vorgeschichte
- diabetes type 2, HTN, hyperlipidemia, hx of stroke, covid Dec 2020
- Andere Medikamente
- losartan, rosuvastatin, trulicity, amlodipine, metformin, hydrochlorothiazide, ergocalciferol, cetirizine, fiber, vitamin C, apple cider vinegar, aspirin
- Allergien
- atorvastatin- myalgias, dehydration
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- Impfdatum
- 08.10.2021
- Beginn
- 08.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site rash
Malaise
Pyrexia
Symptomtext
Pt got fever of 102 and felt like she had covid so she went to urgent care. They gave her medication and steroid. She is feeling better now, but she has a rash at the site of injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- She had a fever of 102 the night getting the vaccine and felt like she had covid so she went to an urgent care center. They gave her medication for the fever and also steroid. She is now better, but has a rash at the site of injection.
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 08.10.2021
- Impfdatum
- 28.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Tenderness
Symptomtext
Patient reports feeling ongoing severe pain and tenderness in left arm from 9-29-21. Has been 10 days after the vaccine was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 02.10.2021
- Beginn
- 03.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site bruising
Injection site erythema
Injection site swelling
Injection site warmth
Symptomtext
no issues immediately following vaccinations, next morning wokeup with redness at injection site and down arm to about her elbow, black and blue at injection site. was red and warm to the touch but not painful. patient iced arm and took tylenol, by the following morning (monday) the swelling went down alot but the black and blue spot at injection site remained
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- crestor,irbesartan,metformin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.02.2023
- Impfdatum
- 24.01.2023
- Beginn
- 24.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No additional AE details or PQC.; PNEUMOVAX 23 was inadvertently administered after it's expiration date; This spontaneous report as received from a licensed practical nurse, referring to a patient of unknown age and gender. Information regarding the patient's pertinent medical history, concurrent condition and concomitant medication was not provided. On 24-JAN-2023, the patient was inadvertently vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) syringe (lot # U010533 with expiration date: 29-OCT-2022; 0.5 milliliter, strength and route were unknown) for prophylaxis (expired product administered). No symptomatic side effects reported during time of report. No additional adverse event (AE) details or product quality complaints (PQC).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.02.2023
- Impfdatum
- 24.01.2023
- Beginn
- 24.01.2023
- 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 details or PQC.; PNEUMOVAX 23 was inadvertently administered after it's expiration date; This spontaneous report as received from a licensed practical nurse, referring to a patient of unknown age and gender. Information regarding the patient's pertinent medical history, concurrent condition and concomitant medication was not provided. On 24-JAN-2023, the patient was inadvertently vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) syringe (lot # U010533 with expiration date: 29-OCT-2022; 0.5 milliliter, strength and route were unknown) for prophylaxis (expired product administered). No symptomatic side effects reported during time of report. No additional adverse event (AE) details or product quality complaints (PQC).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.02.2023
- Impfdatum
- 24.01.2023
- Beginn
- 24.01.2023
- 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 AEs were reported; Expired PNEUMOVAX 23 was administered to a patient.; This spontaneous report was received from a pharmacist and refers to a patient of an unknown age. The patient's medical history, concurrent conditions, concomitant therapies and previous drugs reactions or allergies were not reported. On 24-JAN-2023, the patient was vaccinated with an expired pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) lot #U010533, expiration date: 29-OCT-2022, administered for prophylaxis (strength, and route of administration were not provided) (Expired product administered). No additional adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 21.12.2022
- Impfdatum
- 03.12.2022
- Beginn
- 03.12.2022
- 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; This spontaneous report was received from a pharmacist and refers to a patient of an unknown age and gender. The patient's medical history, concurrent conditions, and concomitant therapies were not reported. On 03-DEC-2022, the patient was vaccinated with an expired dose pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection (lot #U010533, expiration date: 29-OCT-2022) administered for prophylaxis (strength, and route of administration were not provided) (Expired product administered). No additional information was provided to further clarify any details. No additional adverse event (no adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- U
- Eingang
- 09.12.2022
- Impfdatum
- 31.10.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
No additional AE; PNEUMOVAX 23 was administered after the expiry date. Caller did not provide the date administered, the lot or date of expiration; This spontaneous report has been received from a pharmacist referring to a patient of unknown age and gender. The patient's pertinent medical history, drugs reactions or allergies and concomitant medications were not provided. On 31-OCT-2022, the patient was vaccinated with an expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX 23) syringe piston, lot number U010533 has been verified to be a valid lot number with expiration date on 29-OCT-2022, administered as prophylaxis (strength, dose, frequency, route of administration and anatomical location was not provided). There was no previous temperature excursion. No additional adverse events were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.12.2022
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- 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 AEs; an expired dose of PNEUMOVAX 23 was administered on 11/08/2022; This spontaneous report was received from a pharmacy technician and refers to a patient of unknown gender and age. There was no information about the patient's pertinent medical history, concomitant medications or drug reactions and allergies. On 08-NOV-2022, the patient was vaccinated with an expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX 23) prefilled syringe, injection, lot U010533, expiration date 29-OCT-2022 (exact dose, route of administration and anatomical location were not reported) for prophylaxis (Expired product administered). No additional adverse events 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
- MO
- Alter
- -
- Geschlecht
- F
- Eingang
- 06.12.2022
- 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 reported; Pharmacist reports the administration of an expired dose of PNEUMOVAX 23 [ Lot: U010533; Exp:10/29/2022] to a patient on 03NOV2022.; This non-valid spontaneous report was received from a pharmacist, referring to an unspecified patient of unknown age and gender. The patient's pertinent medical history, concurrent conditions, concomitant medications, previous drug reactions, or allergies were not reported. On 03-NOV-2022, the patient was vaccinated with and expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) (strength, vaccination scheme, anatomical site of vaccination and route of administration were not reported; lot number U010533, expiration date reported and validated as 29-OCT-2022) as prophylaxis (expired product administered). No additional adverse event reported (no adverse event). Caller confirmed vaccine was not involved in a temperature excursion and was stored in the recommended storage range until administration. This case was considered non-valid due to the lack of patient's identifiers. Follow up information has been received from the pharmacist on 01-DEC-2022. The patient was a female. This follow up made the case valid due to providing patient's identifier.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.11.2022
- Impfdatum
- 01.11.2022
- Beginn
- 01.11.2022
- 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
Confirmed with caller no other AE occurred; The caller said an expired dose was administered on 11/1/2022; This spontaneous report was received from a pharmacist and refers to a patient of unknown gender and age. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 01-NOV-2022, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23)syringe, injection, 1 dose, lot number u010533, expiration date: 29-OCT-2022, administered for prophylaxis (exact dose, strength, and route of administration were not provided) (expired product administered. No other adverse event occurred (no adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 29.08.2022
- Impfdatum
- 26.08.2022
- Beginn
- 27.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Erythema
Peripheral swelling
Symptomtext
Swollen red arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.08.2022
- Impfdatum
- 14.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
the patient did not experience any side effects or adverse events from the PNEUMOVAX 23.; Medical assistant calling in to report an AE for a patient. Per caller patient received a dose of PNEUMOVAX 23 on 14JUN22022 instead of PREVNAR 13. Caller states that the patient did not experience any side effects or adverse events from the PNEUMOVA; 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 provided. On 14-JUN-2022, the patient was vaccinated with a dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) 0.5 milliliter intramuscularly, lot # U010533, expiration date 29-OCT-2022 for prophylaxis; instead of the intended dose of pneumococcal vaccine conj 13v (crm197) (PREVNAR 13) (wrong product administered). The patient did not experience any side effects or adverse events from the administered vaccine (no adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prophylaxis
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 14.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Hypersensitivity
Peripheral swelling
Symptomtext
PATIENT EXPERIENCE ALLERGIC REACTION RESULTING IN SEVERE SWELLING AND REDNESS UNDERNEATH UPPER LEFT ARM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- HEART DISEASE
- Vorgeschichte
- HEART DISEASE
- Andere Medikamente
- METOPROLOL ER 25MG, ENALAPRIL 2.5, CRESTOR 40, PRASUGREL 10MG
- Allergien
- NO ALLERGIES ON FILE
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
On 3/31/22 it was discovered that the patient has received two doses of Pneumovax 23. One dose was given on 12/5/20 and the other dose was given on 12/28/21. I have tried to reach out to the patient but the phone number says voicemail has not been set up. As far as we know there were no adverse events for receiving the same vaccine twice. We will update when we talk to the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- 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
On 3/31/22 it was discovered that the patient has received two doses of Pneumovax 23. One dose was given on 12/5/20 and the other dose was given on 12/28/21. I have tried to reach out to the patient and had to leave a message. As far as we know there were no adverse events for receiving the same vaccine twice. We will update when we talk to the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- no known
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 01.06.2020
- Beginn
- 13.01.2022
- Tage bis Beginn
- 591,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Wrong product administered
Symptomtext
No additional AE reported; they accidentally administered a second dose of PNEUMOV AX 23 today; This spontaneous report has been received from a medical assistant (MA) and refers to a female patient of unknown age. The patient's pertinent medical history, previous drug reactions or allergies and concomitant medications were not provided. On an unknown date in June 2020, the patient received her first dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) (dose, route of administration, vaccine scheme, lot number, expiration date were not provided). On 13-JAN-2022 (reported as: today), the was accidentally vaccinated with the second dose of the vaccine 0.5 milliliter, once (route of administration and vaccine scheme were not provided; lot number U010533 has been verified to be a valid lot number; expiration date reported and established as: 29-OCT-2022), both as prophylaxis (inappropriate schedule of product administration). No additional adverse events reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 01.06.2020
- Beginn
- 13.01.2022
- Tage bis Beginn
- 591,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Wrong product administered
Symptomtext
No additional AE reported; they accidentally administered a second dose of PNEUMOV AX 23 today; This spontaneous report has been received from a medical assistant (MA) and refers to a female patient of unknown age. The patient's pertinent medical history, previous drug reactions or allergies and concomitant medications were not provided. On an unknown date in June 2020, the patient received her first dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) (dose, route of administration, vaccine scheme, lot number, expiration date were not provided). On 13-JAN-2022 (reported as: today), the was accidentally vaccinated with the second dose of the vaccine 0.5 milliliter, once (route of administration and vaccine scheme were not provided; lot number U010533 has been verified to be a valid lot number; expiration date reported and established as: 29-OCT-2022), both as prophylaxis (inappropriate schedule of product administration). No additional adverse events reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- -
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental exposure to product
Occupational exposure to product
Symptomtext
He also stated that some were splashed onto his skin on his hand; it leaked from the needle due to human error during the administration. He also stated that some were splashed onto his skin on his hand; This spontaneous report was received from a male pharmacist (patient of unknown age) referring to himself. The patient's concomitant medication, pertinent medical history and drug reactions/ allergies were not reported. On 21-DEC-2021, the pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) (lot # U010533, expiration date 29-OCT-2022; strength, dose and route were not reported) was vaccinated to another patient (another linked case) for prophylaxis, some were splashed onto this patient (the pharmacist) skin on his hand (Accidental exposure to product, Occupational exposure to product). This is one of two reports received from the same reporter. ; Sender's Comments: US-009507513-2112USA008400:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental exposure to product
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Needle issue
Symptomtext
No additional AEs were reported; a patient received less than the recommended dose; it leaked from the needle due to human error; This spontaneous report was received from a pharmacist referring to a patient of unknown age. The patient's concomitant medication, pertinent medical history and drug reactions/ allergies were not reported. On 21-DEC-2021 the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) (lot # U010533, expiration date 29-OCT-2022; strength, dose and route were not reported) for prophylaxis, which was less than the recommended dose because it leaked from the needle due to human error during the administration (accidental underdose, needle issue). The pharmacist also stated that some were splashed onto his (pharmacist) skin on his hand (split as another case). No additional AEs were reported. This is one of two reports received from the same reporter. ; Sender's Comments: US-009507513-2112USA009520:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ageusia
Eyelid function disorder
Facial paresis
Symptomtext
34yr old patient with history of obesity, generalized edema, sickle cell trait, HTN, seasonal allergies (on Flonase BID, cetirizine) and other comorbidities presented on 11/23/21 to clinic for well-visit. PA ordered Pneumococcal Polysaccharide 23-valent (Pneumovax-23) LOT # U010533, administered IM in patient's right deltoid by CMA. On 11/26, patient presented at OSH with right sided facial weakness. Symptoms started same day with loss of taste on right side of tongue, inability to close right eye. Patient not started on prednisone at ED as per patient "provider could not see her medical history in system". Patient seen by PA on 11/29 and prescribed Prednisone taper [576853217]. Pneumococcal vaccine added to allergy list.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ageusia
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- vaginal infection
- Vorgeschichte
- unknown
- Andere Medikamente
- flonase BID, cetirizine, chorionicgonadotropin alfa, fluoxetin
- Allergien
- tramadol (dizziness), gardasil (vomitting)
- Vorherige Impfungen
- Gardasil (vomitting)--unknown when immunization given, possibly 2009? patient did not finish series
- Staat
- KS
- Alter
- 0,5
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- 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; she accidentally admnistered PNEUMOVAX 23 to a 6 months old instead of PREVNAR 13; she accidentally admnistered PNEUMOVAX 23 to a 6 months old instead of PREVNAR 13; This spontaneous report was received from a nurse and refers to a 6 month old male patient. The patient's current conditions, pertinent medical history, drug reactions or allergies, and concomitant therapies were not reported. The nurse reported that on 28-OCT-2021, she accidently administered pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) lot number U010533 with expiration date 29-OCT-2022 (dosage, route of administration and anatomical location were not reported) for prophylaxis, to the patient instead of the third dose of pneumococcal vaccine conj 13v (crm197) (PREVNAR 13) (Wrong product administered and product use issue). No additional adverse event (AE) reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 1,5
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
Patient was given a Pneumococcal 23 and should have been given Prevnar 13. At this time, the patient's mom has not reported any problems.
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
- TX
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 20.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Symptomtext
The patient developed erythema 4 to 6 inches below the injection site of PNEUMOVAX 23; This spontaneous report was received from a pharmacist concerning a 67-year-old male patient. Pertinent medical history and concomitant therapy was unknown. There were no drug reactions/ allergies. On 20-OCT-2021, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent)(PNEUMOVAX23) (lot # U010533, expiration date reported and confirm upon internal validation; strength was unknown) 0.5 mL, once, intramuscularly for vaccination. On 21-OCT-2021, the patient developed erythema 4 to 6 inches below the injection site of pneumococcal vaccine, polyvalent (23-valent)(PNEUMOVAX23). The patient saw the pharmacist. The treatment was not given for the events. No lab diagnostics/studies was performed. The outcome of erythema was reported as recovering/resolving. The causality assessment was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 96,0
- Geschlecht
- M
- Eingang
- 07.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Unresponsive to stimuli
Vaccination complication
Symptomtext
PATIENT HAD ADVERSE REACTION TO PNEUMOVAX 23 AND FLUZONE HD VACCINE; FOUND UNRESPONSIVE IN ROOM APPROXIMATELY 11 HOURS LATER; EMS NOTIFIED AND PATIENT TRANSFERRED TO HOSPITAL FOR WEAKNESS DUE TO VACCINE ADMINISTRATION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 2,0
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- PATIENT REPORTED FEELING WELL ON CONSENT FORM
- Vorgeschichte
- DIABETES
- Andere Medikamente
- UNKNOWN; NOT INDICATED ON VACCINATION CONSENT FORM
- Allergien
- NO ALLERGIES TO FOOD, MEDICATIONS, PET OR ENVIRONMENTAL ALLERGIES INDICATED ON CONSENT FORM.
- Vorherige Impfungen
- -