- Staat
- CA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 10.01.2023
- Beginn
- 10.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Lethargy
Muscle spasms
Pain in extremity
Pallor
Presyncope
Seizure
Seizure like phenomena
Tuberculin test
Symptomtext
On 01/10/2023 10:50am 17y/o male patient received 5 injections, Polio, Varicella, T-Dap, MMR and Hepatitis B with PPD. Patient tolerated first 3 vaccinations on the left arm well. Last 2 vaccinations were given on the right arm. PPD was place on the right forearm with complaint of pain but was tolerating well. Patient remained sitting while LVN went to print out the shot record. LVN was standing by the copying machine less than 3 feet away from the exam room with door open. Approximately around 10:55am, patient ?s brother called for help. With exam door open LVN observed patient had seizure like symptom, characterize by convulsing, diaphoresis, closing of eyes and pallor. Convulsion was less than 5 seconds, by the time LVN was in the exam room and beside the patient, muscle spasming has already stopped. LVN called for help immediately and advised patient to breathe through his nose and out through his mouth. Oxygen was given @2L/min via nasal canula. Patient was conscious and responsive. 11:00am LVN went to call Dr for assessment. Dr confirmed that it was vasovagal response and advise that patient could leave once he is able to walk with feeling dizzy. BP was taken every 5 minutes. 100/68 @11:00am. Patient was alert and oriented however, appear lethargic, pale and diaphoretic. Lollipop and Kool-Aid 6.75fl oz was given. After further discussion, patient?s brother stated that the patient has not eaten breakfast/lunch. At 11:07am BP 108/70, O2 was 99% on 2L/min via nasal canula. Color returned and patient stated that he?d felt better with slight dizziness. Patient drank water. BP taken @11:15am 110/72 with O2 discontinued. 11:20am BP 120/78 O2 99% and left the exam ambulating independently. Before leaving LVN advised patient?s brother and father to make sure that patient eats. if further complication arises to take patient to the ER. Patient is scheduled to return on Thursday 01/12/2023 for PPD reading. 01/10/2023 LVN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- NO
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO; MANTOUX
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 02.06.2023
- Impfdatum
- 01.06.2023
- Beginn
- 01.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site swelling
Symptomtext
Localized redness and swelling around the injection site. Ice applied.to reaction site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 23.10.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Dermatitis acneiform
Pyrexia
Rash erythematous
Tenderness
Symptomtext
Fever started 3 days ago, red area with 4 tiny pimples inside, very painful to touch. Physician prescribed po Bactrim today and return precautions. No other symptoms per Mom besides decreased appetite since yesterday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- BRONCHITIS
- Vorgeschichte
- ASTHMA
- Andere Medikamente
- ALBUTEROL SINGULAIR PULMICORT
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site induration
Injection site swelling
Injection site warmth
Symptomtext
Red, raised indurated area developed around 2 injection sites on the left thigh. Pt. was prescribed Bactrim & Keflex in urgent care; symptoms started 9 days after injections. Redness, warmth, swelling decr. after 2 days abx.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- 02/16/2020~DTaP + Hib (no brand name)~3~1.00~Sibling|02/16/2020~Pneumo (Prevnar13)~4~1.00~Sibling|02/16/2020~Measles + Mumps + R
- Staat
- MD
- Alter
- 25,0
- Geschlecht
- U
- Eingang
- 21.11.2023
- Impfdatum
- 09.11.2023
- Beginn
- 09.11.2023
- 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; Pharmacist calling to report an adverse event involving a 25 year old patient who was inadvertently administered an expired dose of MMR II. Pharmacist stated that the MMR II dose had a labeled expiration date of 7/15/2023, and was administered today; This spontaneous report was received from a pharmacist and refers to a 25-year-old patient of unknown gender. The patient's medical history, concurrent conditions, and concomitant therapies were not reported. On 09-NOV-2023, the patient was vaccinated with an expired dose of measles, mumps, and rubella (WISTAR RA 27-3) virus vaccine, live (M-M-R II) injection, therapy type: rHA, two dose series, lot #U022316, expiration date: 15-JUL-2023, administered for prophylaxis (strength, and route of administration were not provided) (Expired product administered). Pharmacist confirmed no report of symptoms or medical concerns at this time from patient involved (No adverse event). Pharmacist stated they were unaware if the dose administered was the first dose the patient has received. No additional information provided regarding this adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 09.11.2023
- Impfdatum
- 09.11.2023
- Beginn
- 09.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
The administered vaccine expired July 15 2023, upon calling the manufacturer the representative stated that according to the stability data they have for MMR II with the above expiration date, the dose is still stable and the patient doesn't need to repeat the dose. Further, upon talking to the patient, she is not experiencing or has experienced any side effects as of now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.09.2023
- Impfdatum
- 31.08.2023
- Beginn
- 31.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
No Adverse Event; Caller reported AE on behalf of an infant patient who was administered an expired dose of MMR-II (no prior TEs). No symptoms reported. Consent to contact HCP was denied. No additional AE/PQC.; This spontaneous report was received from a medical assistant refers to a infant patient of unknown gender. The patient's medical history, concurrent conditions were not reported. The patient's concomitant therapies included STERILE DILUENT. On 31-AUG-2023, the patient was vaccinated with expired dose of measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live, rHA (recombinant Human albumin) (M-M-R II) lot #U022316, expiration date: 15-JUL-2023, 0.5 milliliter (route of administration and anatomical location were not reported) for prophylaxis (expired product administered).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- STERILE DILUENT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.08.2023
- Impfdatum
- 10.08.2023
- Beginn
- 10.08.2023
- 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.; Medical assistant reported that an expired MMR II vaccine was given to a patient today 8/10/2023.; This spontaneous report has been received from a health care professional, regarding a patient of unknown age and gender. The patient's pertinent medical history, previous drug reactions or allergies and concomitant medications were not reported. On 10-AUG-2023, the patient was vaccinated with an expired dose of Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II) subcutaneous injection, as prophylaxis (lot number: U022316, which was determined to be valid, with an expiration date on 15-JUL-2023, therapy type: rHA), with sterile diluent (MERCK STERILE DILUENT) diluent (lot number: W000452, which was determined to be valid, with an expiration date on 23-JUL-2024) (expired product administered) (strengths, doses, schemes, routes and anatomical locations of administration were not reported). No additional event was reported. No further information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prophylaxis
- Vorgeschichte
- -
- Andere Medikamente
- MERCK STERILE DILUENT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.08.2023
- Impfdatum
- 20.07.2023
- Beginn
- 20.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Wrong product administered
Symptomtext
No additional AE/PQC reported.; two patients received expired MMR II vaccine; two patients received expired MMR II vaccine when they were supposed to receive a dose of PROQUAD; This spontaneous report has been received from an other healthcare professional (nurse) referring to patient with unknown gender and age. The patient's concomitant therapies, medical histories and drug allergies were not reported. On 20-JUL-2023, the patient was vaccinated with expired measles, mumps, and rubella (wistar RA 27-3) virus vaccine, live (albumin status recombinant human albumin (rHA)) (M-M-R II) subcutaneous injection, 1 dose, lot # U022316, expiration date: 15-JUL -2023, as prophylaxis (strength and route of administration was not specified), when the patient was supposed to receive a dose of Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD)(fomulation, strength, dose, frequency, lot #, expiry date, indication and route of administration were not provided, the product was not administered) (Expired product administered) (Wrong product administered). No further information available during interaction. No additional adverse events (AEs) were reported (no adverse event), and no product quality complaints (PQCs) were reported. This is one of the two reports received from the same reporter.; Sender's Comments: US-009507513-2307USA011317:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- -
- Geschlecht
- U
- Eingang
- 31.07.2023
- Impfdatum
- 20.07.2023
- Beginn
- 20.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
No adverse event; two patients received expired MMR II vaccine; two patients received expired MMR II vaccine when they were supposed to receive a dose of PROQUAD; This spontaneous report was received from a registered nurse referring to an unknown age and gender patient. The patient's concurrent conditions, medical history, drug reaction or allergies and concomitant therapies were not provided. On 20-JUL-2023, the patient was administered 1 dose of expired vaccine measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live recombinant human albumin (rHA)(M-M-R II) (albumin status rHA) injection, 1 dose, (lot number U022316 has been determined to be valid for measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (M-M-R II), expiration date reported and established as 15-JUL-2023) (strength, and route of administration were not provided), this vaccine was administered instead of Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD) (wrong product administered). No adverse event was reported. This is one of two reports from the same reporter.; Sender's Comments: US-009507513-2307USA011531:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 24.07.2023
- Impfdatum
- 20.07.2023
- Beginn
- 01.07.2023
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient administered MMRII vaccine on 7/20/23 that expired 7/15/23
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 24.07.2023
- Impfdatum
- 20.07.2023
- Beginn
- 01.07.2023
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient given expired (7/15/23) MMR dose on 7/20/23
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 27.06.2023
- Impfdatum
- 11.05.2023
- Beginn
- 11.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Kinrix vaccine given in error instead of DTAP. Error noted during monthly inventory county. Attempted to contact parent. Phone number no longer working. Alert put in child's chart.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- None needed
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None Known
- Allergien
- None Known
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 1,8
- Geschlecht
- F
- Eingang
- 08.02.2023
- Impfdatum
- 08.02.2023
- Beginn
- 01.02.2023
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Administered Kinrix vaccine to child aged 1 year 9 months, later staff entering paperwork informed nurse that I had admnistered a vaccine to child under recommended age,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- UNK
- Vorgeschichte
- UNK
- Andere Medikamente
- UNK
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 21.12.2022
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- 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; Healthcare provider states improperly stored vaccine involved in a temperature excursion was administered to a patient on 28NOV2022. No additional AE reported. No PQC reported. Names of vaccines involved (including lot/exp): MMR II U022316 7/15/; This spontaneous report was received from a medical assistant and refers to a patient of unknown age and gender. The patient's pertinent medical history, concomitant medications, concurrent conditions, and drug reactions/allergies were not reported. On 28-NOV-2022, the patient was vaccinated with improperly stored mumps, and rubella (wistar ra 27-3) virus vaccine, live (recombinant human albumin (rHA)) (M-M-R II) 1 dosage form (dosage reported as "1"), lot # U022315, expiration date 15-JUL-2023 (strength, route of administration and anatomical location were not provided) for prophylaxis (Product storage error). Administered dose of suspect vaccine experienced temperature excursion of 57.49 Fahrenheit (F) for 1 hour and 45 minutes. There was no information about previous temperature excursion and if digital data logger was involved. No additional adverse event reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 07.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Grabbed MMR-V rather than Varicella alone
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- F
- Eingang
- 11.10.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental overdose
No adverse event
Symptomtext
no additional AE have been reported at the time of call.; Nurse practitioner reports an AE for MMRII and VARIVAX. Caller states a 3 year-old patient was inadvertently administered 2 doses of MMRII and 2 doses of VARIVAX concomitantly on 9/28/2022. Caller states no additional AE have been reported at the tim; This spontaneous report was received from a Nurse Practitioner, referring to a 3-year-old female patient. Information regarding medical history, concurrent conditions and concomitant medication was not provided. On 28-SEP-2022, the patient was inadvertently administered 2 doses of measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live(M-M-R II) lot # U022316, expiration date: 15-JUL-2023, 0 .5 milliliter for prophylaxis (dosage information and route of administration not informed), and 2 doses of varicella virus vaccine live (oka/merck)(VARIVAX) 0.5 mL, Lot Number: W012164, expiration date: 12-APR-2024, for prophylaxis(dosage information and route of administration not informed); concomitantly, diluted with sterile diluent, product quantity 4, 0.5 mL (Accidental overdose). No additional adverse event had been reported at the time of call.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental overdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- STERILE DILUENT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 5,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 20.08.2022
- Beginn
- 20.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Wrong product administered
Symptomtext
We gave a 5 year old TDAP instead of DTAP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 5,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 11.05.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Poor quality product administered
Product storage error
Symptomtext
Patient received a sub-optimal COVID-19 vaccine due to a storage and handling error. Vaccine was stored in a regular freezer prior to being refrigerated and then administered. The CDC requested that a VAERS form be submitted for this patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
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- Labordaten
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- Aktuelle Erkrankungen
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- Vorgeschichte
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- Andere Medikamente
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- Allergien
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- Vorherige Impfungen
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