- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 16.07.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Injected limb mobility decreased
Injection site pain
Loss of consciousness
Symptomtext
Pt had severe arm pain (LA) that lasted a couple of days and severely limited mobility, it resolved over time. The couple of days after immunization pt was dizzy and light headed and passed out "a few times". She went to the ER and was released later with all symptoms gone. As of 7/20 pt reports of no problems besides mild arm aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- oxycodone 10
- Allergien
- sulfa, macrodanton
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 23.07.2022
- Beginn
- 23.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Oxygen saturation decreased
Symptomtext
Systemic: Allergic: Difficulty Breathing-Severe, Additional Details: 911 was called when pt reported trouble breathing. EMT came. Her oxygen level was low. Oxygen was given and her O2 went up to 95 after oxygen. They then took her out to the ambulance to check up on the patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 22.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Erythema
Induration
Pain
Paraesthesia
Peripheral swelling
Skin warm
Symptomtext
27yr old patient with history of T1DM and other comorbidities presented to office for Pneumococcal Polysaccharide 23-Valent (Pneumovax-23) on 2/22. Patient previously received Pneumococcal Conjugate 13-Valent (Prevnar 13) on 12/20/21 with no issues. RN administered Pneumococcal Polysaccharide 23-Valent (Pneumovax-23, LOT # U021995) IM in patient's left deltoid. On 2/23 0845, patient contacted office noting "overnight left arm swelling down to elbow, firmness/warmth to touch and redness". Pain 10/10, treated with ibuprofen and ice. In AM, swelling no mid-arm, pain 5/10 with continued warmth/redness and firmness. Virtual visit on 2/23 in which patient noted tingling on left side of face once overnight however, overal In AM, swelling no mid-arm, pain 5/10 with continued warmth/redness and firmness. Virtual visit on 2/23 in which patient noted tingling on left side of face once overnight however, overall swelling and pain improved. Provider recommended cetirizine (dosing not specified), diphenhydramine 25-50mg Q6H PRN itching, and OTC H2 blocker twice daily until symptoms resolved. No further documentation in chart regarding reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 14.11.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site rash
Injection site warmth
Neck pain
Pain
Sensitive skin
Symptomtext
2 hours after vaccination had pain shooting from injection site up the neck. Arm was also sensitive to touch, but not sensitive to movement. Upper right arm was warm and red with rash that was larger than just localized to injection site.. Two days after injection, came to pharmacy was advised to seek medical attention. was prescribed Prednisone 10mg 1-2 qd for 7 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Myrbetriq ER 25mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 15.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Hypoaesthesia
Injection site bruising
Injection site indentation
Injection site pain
X-ray normal
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Severe, Systemic: Numbness (specify: facial area, extremities)-Medium, Additional Details: Patient has pain, severe sensitivity, and tenderness at the injection site. Arm becomes numb during physical activity, like exercise, then becomes sore afterwards. There's a dip/pit in her arm at the injection area which has gotten bigger over time. Her PCP described it as it seems to be "eating away at the muscle & the tissue is disappearing." Her blood work & x-ray came back normal so PCP recommended she see an orthopedic specializing in bone & tissue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 10.08.2022
- Beginn
- 11.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint swelling
Rash
Swelling
Tenderness
Symptomtext
welling under the left arm down to the elbow, pain to the touch and rash down the left arm through the elbow (underside of the arm)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Multiple Sclerosis
- Andere Medikamente
- amantadine, simvastatin, metronidazole cream, citracal slow release, vitamin D3, Vitamin C, Fibercon, Fish Oil, Omeprazole, Famotadine, Prolia, Miralax
- Allergien
- only adhesives and none were applied
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Back pain
Confusional state
Dizziness
Headache
Injection site erythema
Nausea
Pain
Symptomtext
Site: Redness at Injection Site-Mild, Systemic: Body Aches Generalized-Mild, Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: pt complained of lower back pain-Mild, Systemic: Headache-Mild, Systemic: Nausea-Mild, Systemic: Weakness-Mild, Additional Details: EMS was called , symptoms seemed to go away after about 20 minutes of injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 22.03.2022
- Beginn
- 22.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Blood test
Impaired work ability
Sleep disorder
X-ray
Symptomtext
about 4 hours after started with pain in shoulder, really severe shoulder pain, no sleeping, took days off work, still going on and is 9 days later. Went to ED and then orthopedics also to eval what happened
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- xrays, blood work to check for infection
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma, allergies, OAB, MVP, PSVT, GERD
- Andere Medikamente
- Omeprazole, Verapamil, Albuterol, Azelastine, Mometasone, Paroxetine, Cholecalciferol, Cetirizine, Atorvastatin, Fluticasone Propionate, Montelukast, MVI, Vibegron
- Allergien
- Shellfish, Cat dander, Codeine, Dog Dander, Dust Mite, Sulfamethoxale-trimethoprim
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Joint range of motion decreased
Lymphadenopathy
Pain in extremity
Symptomtext
right arm pain redness from the injection site down decreased range of motion swollen lymph nodes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Allergic rhinitis Anticoagulated on Coumadin Anxiety Asthma Atrioventricular canal (AVC) AV block Chronic TMJ pain Desensitization to allergens DVT (deep venous thrombosis) Environmental allergies History of blood clots History of cardiac anomaly History of DVT (deep vein thrombosis)-right upper extremity-2021 History of herpes genitalis-on PCR 7/21 History of menorrhagia-with history of iron deficieny anemia- Dr. follows-controlled with depo- reviewed Dr. note 10/27/21 History of thrombosis-anterior tibial artery -post thrombectomy-2019 Hx of long term use of blood thinners Iron deficiency anemia Left lower lobe pulmonary infiltrate Mild intermittent asthma without complication Palpitations Raynaud's phenomenon 02/07/2020
- Andere Medikamente
- Coumadin 4 mg oral tablet (warfarin), Take one 4mg tablet with one 10mg tablet to equal 14mg on Tues, Thurs, Sat, and Sunday. EpiPen Auto-Injector 0.3 mg injectable kit (EPINEPHrine), 0.3 mg, Intramuscular, Once ipratropium 500 mcg/2.5 mL i
- Allergien
- Mirena Toprol-XL Mucinex ChloraPrep One-Step
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site infection
Injection site swelling
Pain
Symptomtext
Pt. described "whole upper arm redness and swelling, painful to move arm, all per pt.'s report" On ~2/12/21, pt. communicated to clinic that he received antibiotic from an urgi care provider for site infection. On 2/14/22, myself and Dr. examined arm: all reported side effects completely resolved, in terms of observation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Chronic pain
- Vorgeschichte
- Thrombocytopenia, GERD, low back pain; MSK pain, PTSD, somatization disorder, hyperlipidemia, allergic rhinitis
- Andere Medikamente
- ========================================================================= 1) ASCORBIC ACID 500MG TAB Qty: 60 for 30 HOLD Issu:01-11-22 days Sig: TAKE TWO TABLETS BY MOUTH Refills: 2 Last:01-12-22 EVERY DAY F
- Allergien
- Penicillin and penicillin G-related PCNs; haloperidol
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Injection site rash
Pyrexia
Symptomtext
The day after (Saturday, 2/5) I had a fever of about 100 for most of the day, and felt generally crappy. The fever was gone by the following morning and hasn?t returned. I also noticed a rash near the injection site on my right shoulder in the morning on Sunday, 2/6. The rash seems to have mostly gone away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- HIV on ART
- Andere Medikamente
- flaxseed oil 1000 mg PO qday minoxidil topical 5% foam, 1 application topically qday psyllium husk 0.52 gram caps, 2 gram capsules x 5 capsules (10 grams) once per day Triumeq 600-50-300 mg tabs, 1 tab PO qday Vitamin D3 50 mcg (2,000 unit)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Confusional state
Dizziness
Dysstasia
Fall
Fatigue
Nausea
Sleep disorder
Symptomtext
The patient received their vaccine on 01/25/22 and felt fine. she went home, felt normal, ate supper, and went to bed. Around 2 am, husband reported to us that the patient felt tired and weak, fell when she stood up, felt dizzy, and nauseous (did not throw up though). After falling, husband helped her to stand back up. She stated that she felt confused, but then had a glass of water and felt better after about 30 minutes. Today when they called to inform us of what happened, she said she now felt much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- n/a
- Andere Medikamente
- none known
- Allergien
- quinolones, sulfa, cipro, metronidazole
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Injection site urticaria
Muscle tightness
Pain in extremity
Peripheral swelling
Symptomtext
My right arm that was injected with the Pneumonia vaccine was increasingly getting sore throughout the first day and by the night it felt sorer than the average soreness I usually feel from vaccines. The second night, alongside the soreness, I noticed red hives at the top of the right inner part of my right arm and hives on the back of my right arm. I took Benadryl that night to see if the hives would go away. The 3rd day (today) the red hives have spread more on the inner top part of my right arm getting closer to my armpit. My right arm is still sore and the muscle feels tight. My arm also appears swollen where the muscle is tight and the hives are. My left arm with the flu vaccine has no unusual events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Ulcerative Colitis
- Andere Medikamente
- Mesalamine
- Allergien
- No Allergies
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Symptomtext
THE PATIENT CALLED THE OFFICE STATING THE VACCINE INJECTION WAS ITCHY, RED, SWOLLEN. SHE ARRIVED AT 3:15 PM. VITAL SIGNS STABLE, NO RESPIRATORY DISTRESS/SYMPTOMS. THE AREA WAS RAISED/SWOLLEN APPROX. ONE HALF INCH HIGH BY TWO INCHES IN DIAMETER. THE PATIENT STATES SHE NEVER HAD A REACTION TO ANY VACCINE IN HER PAST. DR. EVALUATED THE PATIENT. ICE PACK APPLIED, DISCHARGED TO HOME IN STABLE CONDITION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- AMLODIPINE, QUINAPRIL, ROSUVASTATIN
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- 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 urticaria
Lethargy
Lymphadenopathy
Pyrexia
Symptomtext
Fever, lethargy, swollen lymph nodes beginning evening of 11/9/2021. Pt reports hives on same shoulder as injection site beginning morning after immunization. Treated with ibuprofen and meloxicam. Pt was unable to have scheduled mammogram due to swollen lymph nodes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoporosis
- Andere Medikamente
- None Reported
- Allergien
- Fluroquinolones (Cipro), Flonase
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 05.04.2023
- Impfdatum
- 03.03.2023
- Beginn
- 03.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No additional AE reported; PNEUMOVAX 23 expired on 1/13/2023 and was administered on 3/3/2023; This spontaneous report was received from a pharmacist and referred to a patient of unknown age and gender. The patient's medical history concurrent conditions and concomitant therapies were not reported. On 03-MAR-2023, the patient was vaccinated pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, lot #U021995, expiration date: 13-JAN-2023, administered for prophylaxis (strength, anatomical location and route of administration were not provided) (expired product administered).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 05.04.2023
- Impfdatum
- 03.03.2023
- Beginn
- 03.03.2023
- 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 reported; PNEUMOVAX 23 expired on 1/13/2023 and was administered on 3/3/2023; This spontaneous report was received from a pharmacist and referred to a patient of unknown age and gender. The patient's medical history concurrent conditions and concomitant therapies were not reported. On 03-MAR-2023, the patient was vaccinated pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, lot #U021995, expiration date: 13-JAN-2023, administered for prophylaxis (strength, anatomical location and route of administration were not provided) (expired product administered).
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
- 29.03.2023
- Impfdatum
- 27.02.2023
- Beginn
- 27.02.2023
- 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 reported.; patient was accidently administered an expired dose of PNEUMOVAX 23; This spontaneous report was received from a pharmacist and referred to a patient of unknown age or gender. The patient's medical history, concurrent conditions, concomitant therapies and drug reaction/allergies were not reported. On 27-FEB-2023, the patient was accidently administered an expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, a dosage form, once, lot #U021995, expiration date: 13-JAN-2023, administered for prophylaxis (strength and route of administration were not provided) (expired product administered). The pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) had no prior temperature excursions. No additional adverse event reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 24.03.2023
- Impfdatum
- 03.03.2023
- Beginn
- 03.03.2023
- 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; PNEUMOVAX 23 expired on 1/13/2023 and was administered on 3/3/2023; This spontaneous report was received from a pharmacist, referring to a patient with unknown age and gender. The patient's concomitant therapy, concurrent condition, medical history and drug reactions/allergies were not reported. On 03-MAR-2023, the patient was vaccinated with an expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) (lot number U021995 has been verified to be a valid lot number, expiration date was reported as 13-JAN-2023, dose, route and anatomical location were not provided) for prophylaxis (expired product administered). No additional adverse event (AE) reported (no adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 03.03.2023
- Impfdatum
- 03.03.2023
- Beginn
- 03.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Patient was just administered an expired vaccine and we noticed it a few minutes ago when entering the information into our system. Patient has not yet reported any adverse events and we will follow up with the manufacturer this week to verify the proper course of action moving forward.
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
- 01.03.2023
- Impfdatum
- 13.02.2023
- Beginn
- 13.02.2023
- 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 reported; a dose of PNEUMOVAX 23 was administered after the labeled expiration date.; This spontaneous report was received from a nurse, concerning a patient of unknown age and gender. The patient's pertinent medical history, concurrent conditions, previous drug reactions, allergies, and concomitant medications were not provided. On 13-FEB-2023, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) pre-filled syringe, at a dose of 0.5 milliliter, product quantity: 1, lot #U021995, expiration date: 13-JAN-2023 (route of administration and anatomical location were not provided), administered for prophylaxis (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
- FL
- Alter
- 75,0
- Geschlecht
- U
- Eingang
- 23.02.2023
- Impfdatum
- 07.02.2023
- Beginn
- 07.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
No reported patient side effects.; expired dose of PNEUMOVAX 23 was administered to a patient on 2/7/23 but expired on 1/13/23.; This spontaneous report was received from a pharmacist and referred to a 75-year-old patient of unknown gender. The patient's medical history, concurrent conditions, concomitant therapies, drug reactions and allergies were not reported. On 07-FEB-2023, the patient was vaccinated with an expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23), 0.5 milliliter(mL) injection, 0.5 milliliter, lot #U021995, expiration date: 13-JAN-2023, administered subcutaneously (SQ) for prophylaxis (expired product administered). Pharmacist confirmed that expired vaccine administered had never been stored out of temperature range therefore has never had a temperature excursion. No reported patient side effects. Information regarding revaccination provided to the pharmacist as requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 30.01.2023
- Beginn
- 30.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
The vaccine expired 1-13-2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.01.2023
- Impfdatum
- 20.01.2023
- Beginn
- 20.01.2023
- 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 reported; expired PNEUMOVAX 23 (pfs) was administered to a patient; This spontaneous report has been received from a medical assistant and refers to a patient of unknown age and gender. There was no information regarding the patient's medical history, concurrent conditions and concomitant medications provided. On 20-JAN-2023 (reported also as "today"), the patient was vaccinated with an expired dose of Pneumococcal Vaccine, Polyvalent (23-valent) (PNEUMOVAX 23) injection, lot # U021995 confirmed to be valid with expiration date 13-JAN-2023 (exact dose, route of administration, and anatomical location were not reported), for prophylaxis (expired product administered). The vaccine was stored according to prescribing information through the date of administration. There was no additional adverse event reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- -
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 11.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- 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
2 month old infant was given Pneumovax 23 instead of the ordered Prevnar 13; This non-serious spontaneous case was received during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-JUL-2022 with the following VAERS Primary ID 2290665-01. The original narrative from the sender is as below: 2 month old infant was given Pneumovax 23 instead of the ordered Prevnar 13. Current illness reported as none.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prophylaxis
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 0,2
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 16.02.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 62,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
physician ordered Pneumo 23 instead of Prevnar. This was not caught by the medical assistant at the time. We received a call 4/19/22 from the Health Department when patient was brought in for her 4 month shots there. )it was thought that they completed a VAERS at that time) Received call today that they did not complete one. Patient's mother was informed of the error. No reaction or harm to the infant. Staff re-educated on verifying and having another MA double check all vaccines prior to administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 0,2
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 16.02.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 62,0
- Dosis
- N/A
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
physician ordered Pneumo 23 instead of Prevnar. This was not caught by the medical assistant at the time. We received a call 4/19/22 from the Health Department when patient was brought in for her 4 month shots there. )it was thought that they completed a VAERS at that time) Received call today that they did not complete one. Patient's mother was informed of the error. No reaction or harm to the infant. Staff re-educated on verifying and having another MA double check all vaccines prior to administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 23.05.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 8,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Patient appeared to be due for pneumococcal vaccine. Ordered the vaccine using the ADULT IMM smartset and not the other Smartset New guidelines state for those who have not previously received any pneumococcal vaccine, CDC recommends you give 1 dose of PCV20. For those who have only received PPSV23, CDC recommends you: May give 1 dose of PCV20. PCV20 dose should be administered at least one year after the most recent PPSV23 vaccination. An additional dose of PPSV23 is not recommended since they already received it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.07.2022
- Impfdatum
- 14.03.2022
- Beginn
- 14.03.2022
- 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; Caller is a HCP calling to report a TE for PNEUMOVAX 23; This spontaneous report has been received from a nurse, referring to a patient of unknown age and gender. The patient's concurrent conditions, medical history, concomitant medications, previous drug reactions, or allergies were not provided. On 14-MAR-2022, the patient was vaccinated with an improperly stored dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) (lot number U021995 has been verified to be a valid lot number, expiration date 13-JAN-2023) (strength, dose, frequency, and vaccination scheme were not provided) (product storage error) administered for prophylaxis. The pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) was stored at a temperature of 0 degree Celsius (C) for a time frame of 24 hours. There was a previous temperature excursion. No additional adverse events were reported. This is one of several reports received from the same reporter.; Sender's Comments: US-009507513-2206USA007094: US-009507513-2206USA006587: US-009507513-2206USA006674: US-009507513-2206USA006670: US-009507513-2206USA006770: US-009507513-2206USA006731: US-009507513-2206USA007090: US-009507513-2206USA007068: US-009507513-2206USA006981: US-009507513-2206USA007045: US-009507513-2206USA006852: US-009507513-2206USA007070: US-009507513-2206USA006952: US-009507513-2206USA007059:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.07.2022
- Impfdatum
- 02.03.2022
- Beginn
- 02.03.2022
- 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; PNEUMOVAX 23 was administered to the patient after the excursion occured.; This spontaneous report has been received from a registered nurse, concerning to a patient of unknown age and gender. The patient's pertinent medical history, concurrent conditions, previous drug reactions, allergies, and concomitant medications were not provided. On 02-MAR-2022, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, lot number U021995 which was determined to be valid with expiration date 13-JAN-2023, for prophylaxis, after a temperature excursion of 0 degrees Celsius (C) for a time frame of 168 hours (product storage error) (dose, vaccination scheme, and frequency were not provided). Additionally, no previous temperature excursion was reported. No additional adverse events (AE) were reported. This is one of several reports received from the same reporter.; Sender's Comments: US-009507513-2206USA006587: US-009507513-2206USA007090: US-009507513-2206USA007070: US-009507513-2206USA007059: US-009507513-2206USA007045: US-009507513-2206USA006981: US-009507513-2206USA006952: US-009507513-2206USA006852: US-009507513-2206USA006731: US-009507513-2206USA006674: US-009507513-2206USA007068: US-009507513-2206USA007098: US-009507513-2206USA006770: US-009507513-2206USA006432: US-009507513-2206USA006670:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prophylaxis
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.07.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- 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; PNEUMOVAX 23 was administered to the patient after the excursion occured; This spontaneous report was received from a registered nurse referring to an unknown age and gender patient, whose medical history, concurrent conditions, previous adverse drug reaction, allergies, and concomitant medications were not provided. On 15-MAR-2022, after an excursion took place, the patient was vaccinated with an improperly stored dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23), injection, administered for prophylaxis (lot number: U021995 with an expiration date: 13-JAN-2023 was verified to be a valid lot number; strength, dose, frequency, anatomical injection site, and vaccination scheme were not provided) (product storage error). The dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) was stored in a temperature of 0 degrees Celsius (C) for 24 hours. It was reported that there was a previous temperature excursion. No adverse events were reported. This is one of several reports received from the same reporter.; Sender's Comments: US-009507513-2206USA006770: US-009507513-2206USA006587:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prophylaxis
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.07.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- 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; Caller is a HCP calling to report a TE for PNEUMOVAX 23. During the evaluation the customer reported that the PNEUMOVAX 23 was administered to the patient after the excursion occured. Additional AE filed in 02190216, 02190130, 02190106, 02190106, 02; This spontaneous report has been received from a nurse referring a patient of an unknown age and gender. The patient's medical history, concurrent conditions, concomitant medications and previous drugs reactions or allergies. On 03-MAR-2022, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) lot number U021995, expiration date on 13-JAN-2023 for prophylaxis (strength, formulation, dose, frequency, and route of administration were not reported) that underwent a temperature excursion of 0.3 Celsius grades in 24 hours (product storage error). No additional adverse events were reported. The outcome of the event was not reported. ; Sender's Comments: US-009507513-2206USA006770: US-009507513-2206USA006587: US-009507513-2206USA007098: US-009507513-2206USA007068:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.07.2022
- Impfdatum
- -
- Beginn
- 01.03.2022
- Tage bis Beginn
- -
- 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; Patient vaccinated with product incorrectly stored; This spontaneous report was received from a registered nurse and refers to a patient of unknow age or gender. The patient's medical history, concurrent conditions, and concomitant therapies were not reported. On 01-MAR-2022, the vaccine pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) (lot # U021995, expiration date: 13-JAN-2023) was stored incorrectly for a time frame of 24 hours at a temperature of 0.4?C. There was also a previous temperature excursion. On an unknown date, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection (dose regimen details not provided, lot #U021995, and expiration date: 13-JAN-2023) administered for prophylaxis. No adverse event was provided. ; Sender's Comments: US-009507513-2206USA006587: US-009507513-2206USA006770: US-009507513-2206USA007068:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- -
- Geschlecht
- U
- Eingang
- 25.06.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- 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 additional adverse event; PNEUMOVAX 23 was administered to the patient after the excursion occured/ temperature 0.3C for 24 hours; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. There was no information about the patient's concurrent conditions, concomitant therapies or medical history provided. On 13-APR-2022, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, lot #U021995, expiration date: 13-JAN-2023, administered for prophylaxis (strength, and route of administration were not provided). It was reported that on that day, pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) was administered to the patient after the excursion occurred. Administered dose of vaccine experienced the temperature excursion of 0.3 degrees Celsius for 24 hours (product storage error). Previous temperature excursion was reported as yes. No additional adverse event of product quality complaint were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 0,2
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- -
- Beginn
- 11.05.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
No additional AE reported; Nurse called to report "vaccine error." She stated 2 month old patient was administered PNEUMOVAX 23.; Patient was intended to receive PREVENAR 13; This spontaneous report has been received from a nurse referring a 9-week-old female patient. The patient's pertinent medical history, previous drugs reactions or allergies and concomitant medications were not reported. On 11-MAY-2022, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent)(PNEUMOVAX23) at a dose of 0.5milliliter once, lot number U021995, expiration date: 13-JAN-2023, administered as prophylaxis (route and site of administration were not provided) ; the patient was intended to receive pneumococcal vaccine conj 13v (CRM197) (PREVNAR 13) (product administered to patient of inappropriate age, wrong vaccine administered). No additional adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 08.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Skin warm
Tenderness
Symptomtext
red, warm and tender to touch or use
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- Hypothyroidism HTN Psoriasis
- Andere Medikamente
- B-12 HCTZ Peg prop eye drops Simvastatin Tretinoin cream Triamcinolone cream
- Allergien
- NKDA or food
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Unevaluable event
Symptomtext
Patient had ED visit and/or hospitalization within 6 weeks of receiving COVID-19 vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Duplicate vaccination within the same day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
no additional adverse effect; Incorrect product storage??; This spontaneous report was received from a medical assist concerning a patient of unknown age. No information about the patient's current condition, medical history or concomitant therapy was reported. On 02-DEC-2021, the pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) underwent a temperature excursion (product storage error) and was administered (dose and route were not reported; lot # U021995, 13-JAN-2023) as prophylaxis. This vaccine was stored above 9 degree Celsius (8.6 degree Celsius) for 15 minutes. No previous excursion was reported. No additional adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -