- Staat
- AZ
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 10.01.2023
- Beginn
- 10.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Head injury
Syncope
Symptomtext
Client fainted and fell off the chair in waiting area after receiving vaccines. Client's legs raised while client was lying down. BP 130/80 HR 70. Ice compress placed on head. Provided juice and crackers, which client ate and drank. Client stated she bumped her head when she fell. Client walked to back area after stating she was feeling better. Vitals retaken. Supine: 134/79 HR 69 Sitting: 129/84 HR 62 Advised client and parents of signs of concussion and what to do if signs/symptoms appear . Client voided before being released at 30 minute mark per NP's advisement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 07.06.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Dyskinesia
Loss of consciousness
Seizure like phenomena
Symptomtext
Patient requested to have both shots on the same arm. Menactra was given first then the M.M.R. About 5 to 10 seconds later, he lost consciousness and starting having seizing-like movements which lasted about 20-30 seconds. His mother, who was outside during the vaccine administration, came into the room and patient had a repeat episode in which he woke up about 20-30 seconds later as well. Another pharmacist on duty called EMS to have help dispatched. When they arrived about 5 minutes later, patient was conscious but still feeling dizzy and lightheaded. He was then taken to the hospital via an ambulance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None at this time
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 05.05.2023
- Impfdatum
- 21.04.2023
- Beginn
- 25.04.2023
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Injection site erythema
Injection site mass
Irritability
Symptomtext
Dtap and Hep A were administered at the incorrect interval. Patient had received forth dose of Dtap on 3/21/23 and first dose of Hep A on 3/21/23. Mom called to report a small lump and an area of redness about the size of a pea on the right thigh on 4/25/23. Advised to apply a cold wash cloth and call back if the area of redness increased. Patient seen of other concern on 4/26/23 but reported nodule to right thigh and increased fussiness to provider. 1cm nodule per provider. Advised Tylenol/Ibuprofen for pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- "Cold symptoms" and "long attention span" reported on 3/21/23
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Altered state of consciousness
Disorientation
Dizziness
Fatigue
Hyperhidrosis
Nausea
Pain in extremity
Pallor
Respiratory rate decreased
Speech disorder
Unresponsive to stimuli
Vomiting
Symptomtext
On 11/15/22 patient came in to receive catch-up vaccines. She had one vaccine in the past about one year ago (Tdap). Father did ask about side effects and response if the patient received 8 vaccines. I discussed with the father that we have provided that many vaccines to patients in the past and they did well. But it It?s hard to know because everyone is different. Usual side effects are redness, some swelling at the injection site and the day after some fatigue. I stated that everyone response differently. He chose to do 4 out of the 8 vaccines but the patient wanted and insisted to do all 8 and get them over with so the father decided to do the 8 vaccines to get her caught up. I did educate the patient and father again of side effects-sore arm, and legs. Maybe redness and swelling at the injection site. If she did get a fever to give her Tylenol and or Ibuprofen as directed on the bottle. Patient was educated to drink water- stay hydrated and to move extremities for soreness. Patient and patients father voiced understanding. At approximately 3:25 9 vaccines (Hep A, Hep B, MMR, Varicella, Tdap, IPV, HPV, Menquadfi) were administered to the patient. She received the vaccines in both right/left deltoids and 2 vaccines in both thighs- right and left. A few seconds after the last vaccine administration patient became unresponsive very pale, diaphoretic, and respirations decreased. She would respond to stimuli by opening her eyes. Her face and lips turned pale and she was had slow respirations. I precede to use the ammonia inhalant and that aroused her. Pt was not oriented. She would respond to her name and open her eyes. She was asked to say her name and she was unable to say her name or birthday. She stated she felt nausea and dizzy and wanted to vomit. She was given a few sips of water from her father. He assisted in trying to arouse and talk to her. She then vomited and stated she felt better. She continued to be pale and go in and out of consciousness so I used the ammonia inhalant and that aroused her. At approximately 3:41pm called EMS and I drew up 0.45msl of epinephrine to have on hand. At approximately 3:50 EMS and fire department showed up. I gave them report of the situation and helped move the exam table out to lie the patient down they asked the patients father questions about allergies, last meal. They took vital signs and monitored the patient. After about 35 minutes of the paramedics/ fire department monitoring the patient, she stated she felt better and she sat up. She was able to stand up and walk on her own around the room. At that time the patients father reported he felt comfortable taking the patient home. They set up the next visit in 2 months for one vaccine. I did educate both the patient and father that prior to that appointment make sure the patient has had something to eat, and to come in hydrated. They both voiced understanding. She exited the building ambulating next to her father. EMS and fire department also exited the building approximately the same time 4:25pm. 11/16/22 at approximately 10:52 a.m. I followed up via phone with the patient?s father on how the patient was feeling today. He reported that she stayed home from school because she did vomit in the morning. He reported that the patient stated she?s feeling better, she did report feeling tired and her arms and legs are sore. Re-educated patients? father on the important of movement in the extremities and keeping hydrated as much as possible. He voiced understanding. I did let him know I made a VAERS report and explained that to help. He voiced understanding. VAERS report done on 11/16/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 24.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site nodule
Symptomtext
Bruising and nodule on right thigh developing 1 day after vaccination. Not painful to patient. No other concerns after the vaccine. Has not changed significantly in 2.5 weeks after the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 1,1
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood culture
Culture urine
Differential white blood cell count
Full blood count
Pyrexia
SARS-CoV-2 test
Urine analysis
Vitamin D
Symptomtext
Ongoing fever from date of vaccine until 6/24/22. Temp up to 102.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- CBC w/ diff 6/17/22 Blood Culture 6/17/22 Vitamin D level 6/17/22 Urinalysis 6/24/22 Urine culture 6/24/22 COVID test 6/24/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Patient received her first MMR and Varicella vaccine on 4/22/22. On May 4th we received a call that the patient had broken out in a widespread, non itchy rash on May 2nd 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site cellulitis
Symptomtext
site of injection - cellulitis Hydrocortisone cream OTC Ibuprofen 400 twice daily
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site cellulitis
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- asthma
- Vorgeschichte
- Asthma
- Andere Medikamente
- Proair HFA inhaler
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 7,0
- Geschlecht
- M
- Eingang
- 21.09.2023
- Impfdatum
- 21.08.2023
- Beginn
- 21.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
No additional AE reported; an expired dose of MMR-II was administered to a patient; This spontaneous report as received from a medical assistant referring to an unspecified patient of unknown age and gender. The patient's pertinent medical history, drug reactions/allergies, concurrent conditions and concomitant medications were not reported. On 21-AUG-2023, the patient was vaccinated with expired mumps, and rubella (wistar ra 27-3) virus vaccine, live(M-M-R II) recombinant Human albumin (rHA) lot # U024229 with expiration date 04-AUG-2023, for prophylaxis (strength, dose, route of administration and anatomical location were not reported) (Expired product administered). No additional adverse event (AE) was reported and also no adverse effects were reported. This is a non-valid case as no patient's identifiers were provided. Follow up information has been received from a nurse practitioner regarding a 7-year-old male patient on 14-SEP-2023. The patient had non illness at time of vaccination nor pre-existing physician-diagnosed allergies, birth defects, medical conditions. The vaccine was purchased with public funds and the patient was vaccinated in a public health clinic. On 21-AUG-2023, the patient was vaccinated with first expired mumps, and rubella (wistar ra 27-3) virus vaccine, live(M-M-R II) recombinant Human albumin (rHA) (lot # U024229 with expiration date 04-AUG-2023) (previously reported), administered subcutaneously through left arm. No previous doses of this vaccine was administered before. Outcome for the event was reported as recovered. It was reported that at error occurred at the point of the administration of the vaccine. This event was reported previously to health department. The patient had no response to the administration of the expired vaccine. This case was previously considered non-valid, but upon new follow-up information received patient's identifiers were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- -
- Geschlecht
- M
- Eingang
- 14.09.2023
- Impfdatum
- 12.09.2023
- Beginn
- 12.09.2023
- 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 Event; HCP calling to report an expired MMRII was administered after it expired. Vaccine expired on 8/4/2023. HCP reports the vaccine has not experienced any temperature excursions. No additional AE/PQC.; This spontaneous report as received from a medical assistant refers to a 1-year-old male patient. The patient's medical history and concurrent conditions were not provided. The patient's concomitant therapies included STRILE DILUENT. On 12-SEP-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 #U024229, expiration date: 04-AUG-2023, 0 .5 milliliter (route of administration and anatomical location were not provided) for prophylaxis (expired product administered). It was reported that the vaccine had not experienced any temperature excursions. No additional adverse event reported (no adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- STERILE DILUENT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 04.09.2023
- Impfdatum
- 14.08.2023
- Beginn
- 14.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- 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; patient received an expired dose of MMR II and an expired dose of VARIVAX. The patient received both vaccines on 8/14/2023. The MMR II expired 8/4/2023 and the VARIVAX expired 8/10/2023. Caller stated the pro; This spontaneous report was received from a medical assistant and refers to a 50-year-old female patient. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 14-AUG-2023, the patient was vaccinated with a first dose measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (M-M-R II) injection, which had a lot #U024229, with expiration date: 04-AUG-2023 (Expired drug administered), administered for prophylaxis (strength was not provided); and also vaccinated with a first dose of varicella virus vaccine live (oka/merck) (VARIVAX) injection, lot #U024765, expiration date: 10-AUG-2023 (Expired drug administered), administered for prophylaxis (strength was not provided) both vaccines were given subcutaneously. No treatment was required for the experience. The reporter stated the vaccines had no temperature and the patient had not reported any symptoms or adverse event.
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
- 31.08.2023
- Impfdatum
- -
- Beginn
- 23.08.2023
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
No adverse effects were reported; MMR II was inadvertently administered to a patient today 8/23/2023, and it expired on 8/4/2023; This spontaneous report was received from a physician referring to a 34 year old patient. The patient's medical history, concurrent conditions, historical drugs, and concomitant therapies were not reported. On 23-AUG-2023, the patient was inadvertently vaccinated with an expired dose of measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (M-M-R II) 0.5 milliliter, lot # U024229, expiration date: 04-AUG-2023 (strength, route, dose number, anatomical location and indication were not provided) for prophylaxis (expired product administered). The healt care professional also asked about the need for revaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- -
- Geschlecht
- F
- Eingang
- 29.08.2023
- Impfdatum
- 21.08.2023
- Beginn
- 21.08.2023
- 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 further AE; MMR II expired vaccine given to a patient; This spontaneous report has been received from an administrator 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 21-AUG-2023, the patient was vaccinated with an expired measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live, recombinant human albumin (rha) (M-M-RVAXPRO) injection, one time (valid lot number U024229 [expiration date 04-AUG-2023]) (dose, dose number, frequency, vaccination scheme, route of administration, and anatomical location were not provided) (expired product administered). No side effects. No further adverse event (AE).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 1,0
- Geschlecht
- U
- Eingang
- 23.08.2023
- Impfdatum
- 15.08.2023
- Beginn
- 15.08.2023
- 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 AE/PQC.; Caller reported AE on behalf of a patient who was administered an expired dose of MMR-II (no prior TEs). Caller confirmed that STERILE DILUENT was not expired. No symptoms reported. Obtained consent to contact HCP. No additional AE/PQC.; This spontaneous report was received from a medical assistant regarding 1-year-old patient of unspecified gender. Information regarding medical history, concurrent conditions and concomitant medications was not reported. On 15-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) 0.5ml/dose (lot number U024229 and expiration date 04-AUG-2023 have been confirmed as valid) (no more vaccination details were reported). The reporter confirmed that the STERILE DILUENT was not expired. No symptoms reported. No additional adverse event (AE)/product quality complaint (PQC).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- STERILE DILUENT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- -
- Geschlecht
- U
- Eingang
- 22.08.2023
- Impfdatum
- 11.08.2023
- Beginn
- 11.08.2023
- 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
a dose of MMRII that was administered post expiry. HCP states the MMRII expired on 04AUG2023, and was administered 11AUG2023. HCP states the patient reports no side effects; HCP states the patient reports no side effects; This spontaneous report was received from a pharmacist concerning a patient of unknown age and gender. On 11-AUG-2023 the patient was vaccinated with measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (M-M-R II) albumin status: rHA (recombinant Human albumin), lot# U024229, expiry date: 04-AUG-2023 for prophylaxis (dose and route of administration were not provided) that was administered post expiry date (expired product administered). No side effects were reported by the patient. The product never experienced any temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 5,0
- Geschlecht
- M
- Eingang
- 10.08.2023
- Impfdatum
- 06.08.2023
- Beginn
- 06.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Expired MMR vaccine was inadvertently administered to the patient. No symptoms or adverse effect observed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 05.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 01.01.2023
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Symptomtext
patient was given MMR vaccine IM instead of Sub Q
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Both MMR and Varicella given at 26 days rather than 28 days.
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
- CA
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Timing error. First dose given 08/12/2022, second dose given 09/07/2022, two days prior to eligibility. Child will have to be vaccinated again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 09.07.2022
- Impfdatum
- 09.07.2022
- Beginn
- 09.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
No adverse event
Symptomtext
ADMINISTERED IM INSTEAD OF SQ, NO ADVERSE REACTIONS REPORTED BY PATIENT AT THIS TIME.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Pt given extra doses of each of the above vaccines by mistake. Pt left clinic with no s/s of AE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -