- Staat
- -
- Alter
- 1,1
- Geschlecht
- M
- Eingang
- 30.11.2022
- Impfdatum
- 01.11.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SC / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site pruritus
Papule
Pyrexia
Tremor
Symptomtext
fevers with shaking (unlikely seizures based on description) followed by itching at site of injection and diffusely scattered papules
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- unknown, possible allergic reactions to nuts
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bone pain
Laboratory test
Neck pain
Pain
Paraesthesia
Symptomtext
Soreness, tingling in left hand and left foot, bone pain, neck pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Labs drawn 03/14/2022 at Center
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 1,3
- Geschlecht
- U
- Eingang
- 11.05.2023
- Impfdatum
- 18.04.2023
- Beginn
- 30.04.2023
- Tage bis Beginn
- 12,0
- Dosis
- 2
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Ear infection
Pyrexia
Rash
Rash erythematous
Respiratory tract congestion
Symptomtext
16 month-old here with mother for follow-up on ear infection. Had completed antibiotics x 10 days and no issues at this time. (+) MMR, varicella - given on 4/19/2023 4 days ago, had fever x 2 days and then on third day, had erythematous rash that started on the face and spread to the trunk and extremities. (+) cough and congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- 3/10/23 R Bacterial conjunctivitis
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 1,2
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 26.01.2023
- Beginn
- 26.01.2023
- 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
Patient received 12 month vaccines. Had patient wait 10-15 mins after vaccines were given. Checked patient at 10:40, and noticed patient had redness and slight swelling on right thigh where Varicella vaccine was administered. Called primary provider to get a second look and opinion on thigh. Provider prescribed Benadryl for mild reaction to Varicella vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 26.10.2022
- Impfdatum
- 08.06.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 122,0
- Dosis
- 1
- Route/Site
- SC / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Haemorrhage
Herpes zoster
Pain
Polymerase chain reaction positive
Pustule
Rash erythematous
Skin lesion
Varicella virus test positive
Symptomtext
Developed lesions on the right leg that started 10/8/22 or 10/9/22. Grouped pustules and hemorrhagic vesicles on an erythematous base in a dermatomal distribution with viral PCR positive for VZV consistent with herpes zoster infection. No history of chickenpox but did receive first dose of varicella vaccine approximately 4 months prior. Was given IV acyclovir, treated for aggressive pain control with ice packs/cool compresses and systemic analgesics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- 10/10/2022 - lesion positive for varicella zoster virus (VZV) by PCR
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PCP concern for immunodeficiency. Congenital dermal melanocytosis. Third admission in a year (febrile UTI, COVID, PNA).
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Rash started on forehead on 6/23/2022 and spread to stomach and arms morning of 6/24/2022 when patient was seen in office.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 28.04.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site rash
Rash
Rash erythematous
Rash papular
Symptomtext
Rash started about 12 days after vaccine - papulovesicular rash with slight erythema 8cm x 4cm at injection site R thigh. Spread to trunk after onset
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- mild persistent reactive airway disease J45.30
- Vorgeschichte
- -
- Andere Medikamente
- Budesonide 0.5mg/2ml Albuterol 1.25mg/3ml
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.07.2023
- Impfdatum
- 30.06.2023
- Beginn
- 30.06.2023
- 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 adverse effects; Nurse called regarding MMR II. Nurse reported expired vaccine was administered to a patient. Patient is not reporting signs or symptoms of adverse effects. Expiration date for lot # U017524 was 06/03/2023. Permission to contact HCP was granted. No ad; This spontaneous report was received from a nurse referring to a patient of unknown age and gender. The patient's historical medications, medical history, concurrent conditions and concomitant medications were not reported. On 30-JUN-2023, the patient was vaccinated with an expired dose of measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (rHA)(M-M-R II) lot number U017524, expiration date 03-JUN-2023 (dose and route of administration not reported) for prophylaxis (expired product administered). No adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 03.07.2023
- Impfdatum
- 30.06.2023
- Beginn
- 30.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Patient received expired MMR vaccine during well child clinic visit. No adverse reactions experienced. Provider and parent was notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Iron
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.06.2023
- Impfdatum
- 09.06.2023
- Beginn
- 09.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- 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.; an expired dose of MMR II vaccine was administered to a patient; This spontaneous report was received from a medical assistant referring to a patient of unknown gender and age. The patient's medical history, concurrent conditions or concomitant therapies were not reported. On 09-JUN-2023, the patient was vaccinated with 1 dose of measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (M-M-R II) injection, lot #u017524, expiration date: 03-JUN-2023 (strength, route of administration, and indication were not provided) (expired product administered). 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
- NM
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 14.06.2023
- Impfdatum
- 07.06.2023
- Beginn
- 07.06.2023
- 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
No adverse event
Symptomtext
No additional AE; HCP called to report inadvertent administration of an expired dose of MMR II. MMR II expired on 6/3/2023 and was administered on 6/7/2023.; This spontaneous report was received from a registered nurse referring to a 12-month-old male patient. The patient's medical history, historical drugs, past drug reactions or allergies, concurrent conditions, and concomitant drugs were not reported. On 07-JUN-2023, the patient was vaccinated with Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II) (rHA) injection (0.5 ml, lot#: U017524, expiration date: 03-JUN-2023; strength was not reported) orally for prophylaxis (expired product administered). No adverse effects 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
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 14.06.2023
- Impfdatum
- 09.06.2023
- Beginn
- 09.06.2023
- 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/PQC.; Caller reported inadvertent administration of MMR-II 6 days post-expiry; This spontaneous report has been received from a medical assistant regarding a patient of unknown age and gender. The patient's pertinent medical history, concurrent conditions, concomitant medications, and drug reactions or allergies were not provided. On 09-JUN-2023, the patient was vaccinated with measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (M-M-R II) injection, 0.5 milliliters (ml) and sterile diluent (dose number, frequency, vaccination scheme, route of administration, anatomical location, lot number, and expiration date were not provided) 6 days post-expiry (expired product administered) with no known temperature excursion (TE). No reported symptoms at time of call. No additional adverse event (AE).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- STERILE DILUENT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.06.2023
- Impfdatum
- 05.06.2023
- Beginn
- 05.06.2023
- 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 dose of MMR II was administered to a pediatric patient today.; This spontaneous report was received from a medical assistant and refers to a patient of unknown age and gender. No information on patient's medical history, current conditions and concomitant medications was provided. On 05-JUN-2023, the patient was vaccinated with dose of expired measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (M-M-R II) lot #U017524 and expiration date 03-JUN-2023, 0.5 milliliter for prophylaxis (route of administration, strength and dose number were not provided) (expired product administered and 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
- 16.03.2023
- Impfdatum
- 17.02.2023
- Beginn
- 17.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
No adverse event
Symptomtext
no adverse event; A pharmacist reported that a dose of MMR II vaccine was administered to a patient via the intramuscular route instead of the subcutaneous route; This spontaneous report was received from a pharmacist referring to a patient of unknown age and gender. The patient's medical history, concurrent conditions, drug reactions/allergies and concomitant therapies were not reported. On 17-FEB-2023, the patient was vaccinated with a dose of measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live recombinant Human albumin (rHA) (M-M-R II) use as directed to prevent measles, mumps and rubella infection as prophylaxis, lot #U017524, expiration date: 03-JUN-2023 (strength was not provided), via the intramuscular route instead of the subcutaneous route (incorrect route of product administration). There was no additional adverse event (no adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 02.03.2023
- Impfdatum
- 27.01.2023
- Beginn
- 27.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Infanrix vaccine administered prior to four to six month interval. Administered at 3mo, 1weeks. No adverse reaction from patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.02.2023
- Impfdatum
- 06.02.2023
- Beginn
- 06.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
No additional AE or PQC reported; HCP reported MMR II was inadvertently administered with PROQUAD. No additional AE or PQC reported. No additional information provided.; This spontaneous report was received from a nurse and refers to a patient of unspecified age and gender. The patient's concomitant medications, pertinent medical history, concurrent conditions, drug reactions or allergies were not reported. On 06-FEB-2023, the patient was inadvertently vaccinated with measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (rHA) (M-M-R II) subcutaneous injection, lot #U017524, expiration date: 03-JUN-2023 (strength, and route of administration were not provided) and measles, mumps, rubella and varicella (oka-merck) virus vaccine live (rHA) (PROQUAD) subcutaneous injection, lot #W017572, expiration date: 29-NOV-2023 (strengths, doses, vaccination schedules, sites and route of administration were not provided) for prophylaxis (Accidental overdose). No additional adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 02.02.2023
- Impfdatum
- 19.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Decreased appetite
Developmental regression
Fall
Gait disturbance
Irritability
Orthostatic intolerance
Sleep disorder
Symptomtext
Regression of walking, unsteadiness standing and while cruising or stepping (improved 1/31) Tendency for falling backwards Intolerance of being brought down to supine position (resolved on 1/30) Reduced appetite for solids and reduced appetite for milk (improved 2/1) Irregular sleep pattern Fussy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Balance disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Vitamin D intermittently, stopped since the 19th. They were focusing on outdoor time instead. Topical antifungal (MUAid) started 30th
- Allergien
- none
- Vorherige Impfungen
- colic, pediarix at age 3 months
- Staat
- CA
- Alter
- 1,1
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 25.01.2023
- Beginn
- 25.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Swelling
Symptomtext
Patient had slight swelling and redness. Was given 2.5mL of12.5mg/5mL of Benadryl P.O x1 in office. Lot: 1HK0857 EXP: 06/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 17.01.2023
- Impfdatum
- 17.01.2023
- Beginn
- 17.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
patient should have received Tdap but instead received Dtap.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 1,2
- Geschlecht
- M
- Eingang
- 13.01.2023
- Impfdatum
- 13.01.2023
- Beginn
- 13.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Needle issue
Syringe issue
Symptomtext
Needle was not in all the way and gave vaccine. However, vaccine liquid leaked through between needle and syringe.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Needle issue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 20.12.2022
- 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
Accidental underdose
No adverse event
Product administered to patient of inappropriate age
Underdose
Symptomtext
No additional AE reported; during administration of MMR II dose, patient moved her leg and she only received about half the dose; This spontaneous report was received from a medical assistant student and refers to a 2-year-old female patient. The patient's medical history, concurrent conditions and concomitant medications were not provided. On 28-NOV-2022, the patient was vaccinated with a dose of measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (rHA)(M-M-R II) subcutaneous injection, 0.5 ml, lot # U017524, expiration date: 03-JUN-2023, administered for prophylaxis (strength, and route of administration were not provided) reconstituted with a sterile diluent (Inappropriate age at vaccine administration). During administration of measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (rHA)(M-M-R II) dose, the patient moved her leg and she only received about half the dose (Accidental underdose). Agent confirmed there was nothing wrong with the product. No additional AE reported. This is one of 2 reports received from the same reporter.; Sender's Comments: US-009507513-2212USA000351:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 1,3
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 21.09.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
patient had no Symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 30.09.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
CMA accidentally administered Pfizer as second dose in COVID vaccine series when patient received Moderna as first dose. First dose of Moderna vaccine administered on 7/23/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 0,9
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 16.08.2022
- Beginn
- 16.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
No adverse symptoms noted. Vaccines were administered five days earlier than minimum valid date. Provider in office was notified. Father was also notified while in office and advised vaccines will need to be given again. Father educated to monitor for signs of adverse reactions and advised to report them. Father verbalized understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 1,9
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Pt received extra dose of Varicella, MMR, and PCV13
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE
- Andere Medikamente
- UKNOWN
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect route of product administration
Symptomtext
Vaccination completed IM instead of SC on patient's right arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 23.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Computerised tomogram head
Electrocardiogram
Full blood count
Hypotonia
Unresponsive to stimuli
Urine analysis
Symptomtext
Patient was found unresponsive at 6:00am this morning when mom went to wake her for the day. She was limp, breathing normally, and taken immediately to the local Emergency Room when she finally came around after a little while. Further work up/evaluation is currently being done
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Computerised tomogram head
- Hospital-Tage
- -
- Labordaten
- CBC, Urinalysis, Head CT, EKG 2/24/2022 Other tests possibly pending depending on results and patient
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -