- Staat
- ME
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 29.12.2022
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Immediate post-injection reaction
Loss of consciousness
Symptomtext
Patient felt lightheaded immediately after receiving Japanese Encephalitis vaccine. This vaccine was the fifth and last vaccine given on 12/28/2022. Patient received vaccine at 4:07 PM and immediately felt lightheaded. Patient was seated on exam table and began to pitch his body forward. Patient was able to lay back on exam table with his feet up. Patient did not lose consciousness and continued to speak with this RN. Patient was provided with a cool compress for his forehead. Patient remained supine for 10 minutes and then patient reported he felt better and was able to sit up and walk without experiencing any dizziness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None needed.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Mixed hyperlipidemia, Hematochezia, Constipation, Microhematuria, Renal cyst, Urinary frequency, Insomnia, Acne
- Andere Medikamente
- Received Hepatitis A, Typhoid, MMR, and COVID-19 booster on 12/28/2022 as well. No medications, supplements, herbal remedies taken at the time of vaccination.
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Chest discomfort
Dizziness
Headache
Hot flush
Hypoaesthesia
Limb discomfort
Nausea
Paraesthesia
Symptomtext
After administering Tdap and Hep A, patient complained of headache, hot flashes, dizziness, nausea. Shortly after she complained of her chest feeling weird, numbness in hands. Patient later stated her feet were tingling and legs were heavy. Patient did say her stomach hurt. Patient was given crackers and juice. Checked vitals, called EMS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Provider gave Epinephrine 0.3 mg.
- Aktuelle Erkrankungen
- Abdominal mass, unspecified abdominal location Acute pharyngitis, Virial URI with cough, Pansinusitis
- Vorgeschichte
- Asthma
- Andere Medikamente
- -
- Allergien
- Ventolin, Adhesive, Baclofen
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Hypoaesthesia
Immediate post-injection reaction
Injected limb mobility decreased
Joint range of motion decreased
Pain in extremity
Sensory disturbance
Symptomtext
Immediately following vaccination with Hep A #1 on 04/11/2022, pt reported that her left arm became "numb" and stated that she was unable to move this extremity. Pt asked husband to massage arm while RN obtained an ice pack from vaccine room. Upon coming back to room, pt able to move L arm in a circle. Pt reported that pain began resolving with movement and application of ice. Pt declined opportunity to speak with RN's supervisor. Pt stated that shoulder joint hurt, reporting it "felt like my arm fell out of my socket" while arm was dangling for vaccine administration. RN instructed pt to follow up with provider or urgent care if pain worsens or does not resolve; pt verbalized understanding. RN contacted pt on 04/12/2022 at 11:15 to follow up on pt's report of arm numbness and decreased ROM following vaccination on 4/11/22. During phone call, pt reported that she had improved ROM and less pain in L arm on 04/12/2022. Pt stated that she has bad joints, which she believes caused pain after vaccination after arm was hanging at her side for vaccination. Pt reported that she does not believe the vaccine administration itself caused pain. RN counseled pt to follow up with PCP or urgent care if pain does not resolve and/or if ROM affected; pt verbalized understanding, denied questions or concerns at that time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- During screening, pt reported developing a fever ("about 101.9 degrees") and fatigue on 04/06/2022. Pt stated fever resolved "a couple days ago." Pt reported that s/sx resolved and denied feeling ill on date of vaccination. Per nurse supervisor, okay to vaccinate this pt for Hep A despite pt having sx last week, as sx onset not within incubation period for Hep A. Per supervisor, this guidance came from CDC and agency's medical directior on 04/08/2022 to vaccinate for Hep A as long as pt does not present with severe sx.
- Vorgeschichte
- Pt reports hx of T2 DM and COPD.
- Andere Medikamente
- Pt reports taking the following medications regularly: gabapentin 500 mg BID, levothyroxine once daily (dosage unknown), BP medication "325/25" once daily (medication name unknown), allopurinol 300 mg once daily, and metformin 500 mg BID.
- Allergien
- Pt reports allergy to PCNS, states sx of rxn include pruritis.
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 30.11.2023
- Impfdatum
- 14.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
Pain in extremity
Sleep disorder
Symptomtext
Reported Symptoms: 10003239:ARTHRALGIA; Narrative: Other Relevant HX: 8/14/23 PACT CPP: "Patient reports since last COVID booster has had chronic arm pain and cannot sleep on the side - has not tried anything for the pain" No other documentation of arm pain from vaccines in 6/2022 in system. Patient did receive two vaccines in same arm according to documentation on that day (COVID booster and Hep A). Other:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 11.08.2023
- Impfdatum
- 06.07.2023
- Beginn
- 06.07.2023
- 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
Pain in extremity
Wrong product administered
Symptomtext
1) Patient received an expired Hep A vaccine. Expired 6/17/23. Hep A was administered 7/6/23. 2) RN intended to administer Hepatitis B shot. Patient received wrong medication. She received the Meningitis B shot. Patient c/o sore arm. Patient came back to the public health clinic 7/18/23 and received an up to date Hep A and Hep B vaccine at no charge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 1,6
- Geschlecht
- M
- Eingang
- 09.02.2023
- Impfdatum
- 08.02.2023
- Beginn
- 08.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abnormal behaviour
Decreased interest
Incorrect dose administered
Lethargy
Product administered to patient of inappropriate age
Pyrexia
Symptomtext
Pt given adult dose of vaccine versus peds dosing. No issues with 15 minutes of vaccine. Per Father patient did have fever at home, was whiney and did more hand holding than normal, was "unlike himself". Per Mother patient was feverish and lethargic, disinterested in stuff similar to past vaccinations, no reaction at injection site. Per Father and Mother fever controlled with Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- PFO (patent foramen ovale)
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 03.08.2022
- Impfdatum
- 26.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Incorrect dose administered
Irritability
Product administered to patient of inappropriate age
Symptomtext
Pediatric patient was inadvertently given adult dose of Hep A. Error was noticed right away, mom was notified and site was consulted as well as the nurse on duty. The website advised to monitor the child, the dose given counts as dose #1 and does not affect the timing on dose #2. Mom called 2 days later (7/28/22) and reported diarrhea and some crankiness. Nurse advised BRAT diet for diarrhea, and continue monitoring.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 08.11.2023
- Impfdatum
- 21.06.2023
- Beginn
- 21.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
inadvertently administered an expired Havrix; This non-serious case was reported by a nurse via call center representative and described the occurrence of expired vaccine used in a 29-year-old male patient who received HAV (Havrix) (batch number NZ7GR, expiry date 17-JUN-2023) for prophylaxis. On 21-JUN-2023, the patient received Havrix. On 21-JUN-2023, an unknown time after receiving Havrix, the patient experienced expired vaccine used (Verbatim: inadvertently administered an expired Havrix). The outcome of the expired vaccine used was unknown. Additional Information: GSK receipt date: 30-Oct-2023 The registered nurse called to inquired that it was still good or they should revaccinate. The reporter did not consent to follow-up. The patient received an expired dose of Havrix, which led to expired vaccine used.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 24.08.2023
- Impfdatum
- 23.06.2023
- Beginn
- 23.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
a patient was administered a dose of Havrix that was expired; This non-serious case was reported by a other health professional via call center representative and described the occurrence of expired vaccine used in a 19-year-old female patient who received HAV (Havrix) (batch number NZ7GR, expiry date 17-JUN-2023) for prophylaxis. On 23-JUN-2023, the patient received Havrix. On 23-JUN-2023, an unknown time after receiving Havrix, the patient experienced expired vaccine used (Verbatim: a patient was administered a dose of Havrix that was expired). The outcome of the expired vaccine used was unknown. Additional Information: GSK Receipt Date: 21-AUG-2023 The reporter was a Medical Assistant. The reporter consented to follow up. The Vaccine Administration Facility was the same as Primary Reporter. The reporter reported that a patient was administered a dose of Havrix that was expired, which led to expired vaccine used.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 14.08.2023
- 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
Symptomtext
patient received Havrix on 10AUG2023 that expired on 17JUN2023; This non-serious case was reported by a other health professional via call center representative and described the occurrence of expired vaccine used in a 25-year-old female patient who received HAV (Havrix 1440 adult) (batch number NZ7GR, expiry date 17-JUN-2023) for prophylaxis. On 10-AUG-2023, the patient received Havrix 1440 adult. On 10-AUG-2023, an unknown time after receiving Havrix 1440 adult, the patient experienced expired vaccine used (Verbatim: patient received Havrix on 10AUG2023 that expired on 17JUN2023). The outcome of the expired vaccine used was unknown. Additional Information: Receipt Date: 10-AUG-2023 The health care professional (HCP) reported that the patient received a dose of Havrix on 10th August 2023 which was expired on 17th June 2023, which led to expired vaccine used. The reporter consented to follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 04.08.2023
- Impfdatum
- 30.07.2023
- Beginn
- 30.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired Product Use; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of expired vaccine used in a 47-year-old male patient who received HAV (Havrix) (batch number NZ7GR, expiry date 17-JUN-2023) for prophylaxis. On 30-JUL-2023, the patient received Havrix. On 30-JUL-2023, an unknown time after receiving Havrix, the patient experienced expired vaccine used (Verbatim: Expired Product Use). The outcome of the expired vaccine used was unknown. Additional Information: GSK Receipt Date: 31-JUL-2023 The pharmacist reported the patient was administered a dose of Havrix, which had an expiration date of 17 June 2023, which led to expired vaccine used. The pharmacist was unsure which dose number this was in the series. At the time of reporting, the dose was not repeated. The reporter consented to follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 01.08.2023
- Impfdatum
- 28.07.2023
- Beginn
- 28.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
expired drug used; This non-serious case was reported by a other health professional via call center representative and described the occurrence of expired vaccine used in a 54-year-old female patient who received HAV (Havrix) (batch number NZ7GR, expiry date 17-JUN-2023) for prophylaxis. On 28-JUL-2023, the patient received Havrix. On 28-JUL-2023, an unknown time after receiving Havrix, the patient experienced expired vaccine used (Verbatim: expired drug used). The outcome of the expired vaccine used was unknown. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 28-JUL-2023 The reporter was a medical assistant. The reporter did not consent to follow-up. The Vaccine Administration Facility was the same as Primary Reporter. The reporter stated that a patient inadvertently received an expired dose of Havrix, which led to expired vaccine used.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 18.07.2023
- Impfdatum
- 22.06.2023
- Beginn
- 22.06.2023
- 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
Symptomtext
Pt was administered expired vaccine-reported to GSK.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Descovy, Vitamin D3
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 05.07.2023
- Impfdatum
- 26.06.2023
- Beginn
- 26.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
expired dose administered; This non-serious case was reported by a other health professional via call center representative and described the occurrence of expired vaccine used in a 44-year-old male patient who received HAV (Havrix) (batch number NZ7GR, expiry date 17-JUN-2023) for prophylaxis. On 26-JUN-2023, the patient received Havrix. On 26-JUN-2023, an unknown time after receiving Havrix, the patient experienced expired vaccine used (Verbatim: expired dose administered). The outcome of the expired vaccine used was unknown. Additional Information: GSK receipt date: 26-JUN-2023 The reporter consented to follow up via email. The vaccine administration facility was the same as primary reporter. The patient received an expired dose of Havrix, which led to expired vaccine used.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 27.06.2023
- Impfdatum
- 22.06.2023
- Beginn
- 22.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
expired dose administered; This non-serious case was reported by a nurse via call center representative and described the occurrence of expired vaccine used in a 45-year-old male patient who received HAV (Havrix) (batch number NZ7GR, expiry date 17-JUN-2023) for prophylaxis. On 22-JUN-2023, the patient received Havrix. On 22-JUN-2023, an unknown time after receiving Havrix, the patient experienced expired vaccine used (Verbatim: expired dose administered). The outcome of the expired vaccine used was unknown. Additional Information: GSK receipt date: 22-JUN-2023 The vaccine administration facility was the same as primary reporter. The reporter consented to follow-up via email. The patient received an expired dose of Havrix, which led to expired vaccine used.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 27.06.2023
- Impfdatum
- 22.06.2023
- Beginn
- 22.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Havrix was administered today on June 22 2023. Havrix expired on June 17th 2023; This non-serious case was reported by a nurse via call center representative and described the occurrence of expired vaccine used in a 38-year-old male patient who received HAV (Havrix) (batch number NZ7GR, expiry date 17-JUN-2023) for prophylaxis. On 22-JUN-2023, the patient received Havrix. On 22-JUN-2023, an unknown time after receiving Havrix, the patient experienced expired vaccine used (Verbatim: Havrix was administered today on June 22 2023. Havrix expired on June 17th 2023). The outcome of the expired vaccine used was unknown. Additional Information: GSK Receipt Date: 22-JUN-2023 The reporter consented to follow up. Preferred follow up via email. On the day of reporting, the patient received an expired dose of Havrix, which led to expired vaccine used.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 27.06.2023
- Impfdatum
- 20.06.2023
- Beginn
- 20.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
inadvertently administered an expired Havrix; This non-serious case was reported by a other health professional via call center representative and described the occurrence of expired vaccine used in a 61-year-old female patient who received HAV (Havrix adult) (batch number NZ7GR, expiry date 17-JUN-2023) for prophylaxis. On 20-JUN-2023, the patient received Havrix adult. On 20-JUN-2023, an unknown time after receiving Havrix adult, the patient experienced expired vaccine used (Verbatim: inadvertently administered an expired Havrix). The outcome of the expired vaccine used was unknown. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK receipt date: 20-JUN-2023 It was reported that a patient was inadvertently administered an expired Havrix which led to expired vaccine used. The reporter enquired that should the patient be revaccinated. The reporter did not consent to follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 23.06.2023
- Impfdatum
- 22.06.2023
- Beginn
- 22.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Patient has no none adverse event but was made aware that the Havrix that was given on 06/22/23 had expired on 06/17/2023. Patient expressed no concerns or side effects from vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HIV AIDS vitamin d deficiency anemia seasonal allergic rhinitis hypertension bask spasms diabetes
- Andere Medikamente
- Biktarvy Cholecalciferol Ferrous Sulfate Fluticasone Hydrochlorothiazide Methocarbamol Pravastatin Metformin Lisinopril Amlodipine
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 22.06.2023
- Impfdatum
- 19.06.2023
- Beginn
- 19.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
administered an expired dose of Havrix; This non-serious case was reported by a other health professional via call center representative and described the occurrence of expired vaccine used in a 71-year-old male patient who received HAV (Havrix) (batch number NZ7GR, expiry date 17-JUN-2023) for prophylaxis. On 19-JUN-2023, the patient received Havrix. On 19-JUN-2023, an unknown time after receiving Havrix, the patient experienced expired vaccine used (Verbatim: administered an expired dose of Havrix). The outcome of the expired vaccine used was unknown. Additional Information: GSK receipt date: 20-JUN-2023 Follow-up ok, HCP facility address and email are in HCP details. The reporter consented to follow up. The patient received an expired dose of Havrix, which led to expired vaccine used
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 06.06.2023
- Impfdatum
- 05.06.2023
- Beginn
- 05.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
MA Administered vaccines below from the adult state stock to a 16 year old patient with no insurance. Provider will contact patient. - Hep A Havrix adult, Hep B Heplisav Adult, HPV Gardasil 9, and TDAP Boostrix
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 21.02.2023
- Impfdatum
- 15.02.2023
- Beginn
- 15.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Vaccination error
Symptomtext
Hep A dose #2/2 was given too early. It was due March 1st, 2023 and given 2/15/2023. Pt notified while in clinic of the error and understands he will need to repeat the dose 8/15/2023 or later to be a valid dose. Pt verbalizes understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 01.11.2022
- Beginn
- 10.01.2023
- Tage bis Beginn
- 70,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Depression
Feeling abnormal
Symptomtext
I started to have really bad depression. After about 2 and a half weeks, I went to see the doctor. She did not provide any treatment. She told me to go to see my PCP I scheduled an appointment with my primary care doctor. I am still feeling low, and nothing makes sense. I am still having the same feelings.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Depression
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HIV
- Andere Medikamente
- Vitamin B complex; DOVATO
- Allergien
- N/A
- Vorherige Impfungen
- Flu vaccine 09/2022, chills, headache, tired and other mild symptoms, lasted for 3 to 4 days
- Staat
- MI
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 18.01.2023
- Impfdatum
- 16.01.2023
- Beginn
- 16.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
A pediatric dose of HepB was accidentally administered to client instead of an adult dose. Client was contacted and informed of the incident. Staff also explained that because it was a pediatric dose, it would be considered invalid and he would need to receive an adult dose of HepB to complete the series. Staff scheduled client an appointment on 1/18/23 and an adult dose of HepB was administered. Second, the HPV9 was pulled from the inventory and it should have been taken from the private vaccine inventory. Due to client's age, he does not qualify for program. This dose will be replaced with private pay and private vaccine loss report will be completed by my supervisor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None reported.
- Vorgeschichte
- None reported.
- Andere Medikamente
- None reported.
- Allergien
- None reported.
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
1st dose on 12Oct2022, 2nd on 12Nov2022; This case was reported by a other health professional via call center representative and described the occurrence of drug dose administration interval too short in a 60-year-old female patient who received HAV (Havrix) (batch number NZ7GR, expiry date 17th June 2023) for prophylaxis. Concomitant products included HEPATITIS A VACCINE (HAVRIX), HEPATITIS B VACCINE (ENGERIX B) and HEPATITIS B VACCINE (ENGERIX B). On 12th November 2022, the patient received the 2nd dose of Havrix. On 12th November 2022, unknown after receiving Havrix, the patient experienced drug dose administration interval too short. On an unknown date, the outcome of the drug dose administration interval too short was unknown. Additional Information: GSK receipt date: 01-DEC-2022 Reporters comment: The reporter reported that patient received the 1st dose of Havrix and an early 2nd dose of Havrix. The patient also received the 1st and 2nd dose of Engerix on the same dates. The reporter consent to follow up. Additional Supportive information: The patient received 2nd dose of havrix, earlier than the recommended interval, which led to shortening of vaccinations schedule. This case had been linked with US2022180223 same reporter. Note-As per source document Engerix B coded as concomitant vaccine.; Sender's Comments: US-GSK-US2022180223:Same reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
F1st dose of Havrix on 12Oct2022 and an early 2nd dose on 12Nov2022.; This case was reported by a other health professional via call center representative and described the occurrence of drug dose administration interval too short in a 72-year-old female patient who received HAV (Havrix) (batch number NZ7GR, expiry date 17th June 2023) for prophylaxis. Concomitant products included HEPATITIS A VACCINE (HAVRIX), HEPATITIS B VACCINE (ENGERIX B) and HEPATITIS B VACCINE (ENGERIX B). On 12th November 2022, the patient received the 2nd dose of Havrix. On 12th November 2022, unknown after receiving Havrix, the patient experienced drug dose administration interval too short. On an unknown date, the outcome of the drug dose administration interval too short was unknown. Additional Information: GSK receipt date: 01-DEC-2022 Reporters comment: The patient also received the 1st and 2nd dose of Engerix on the same dates of Havrix on 12th October 2022 and 12th November 2022. The reporter reported that patient received the 1st dose of Havrix and an early 2nd dose. The reporter consent to follow-up. Additional Supportive information: The patient received the 2nd dose earlier than the recommended interval, which led to shortening of vaccinations schedule. ; Sender's Comments: US-GSK-US2022180225:Same reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- HAVRIX; ENGERIX B; ENGERIX B
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 05.12.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
The client got an adult vaccine and should have been pediatric dose client was notified he was ok with the error. No signs or symptoms were noted by the client.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 18.11.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administration error
Wrong product administered
Symptomtext
Patient had requested hepatitis B vaccine and was given hepatitis A vaccine in error. He has been notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administration error
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None indicated on screening form
- Vorgeschichte
- None indicated on screening form
- Andere Medikamente
- Unknown
- Allergien
- None indicated on screening form
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 03.11.2022
- Impfdatum
- 02.11.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
Adolescent received one dose of adult Hepatitis A vaccine. Patient was monitored for 30 minutes under supervision of two nurses with no signs and symptoms after observation. No treatment needed. Patient was released to guardian care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
pt was given an extra dose of Hepatitis A. Did not need the third dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Hepatitis C, Psychosis
- Vorgeschichte
- Hepatitis C and psychosis
- Andere Medikamente
- Olanzapine
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 17.08.2022
- Impfdatum
- 15.08.2022
- Beginn
- 15.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
Hepatitis A vaccine was given instead of intended Hepatitis B vaccine. No adverse reactions reported by patient. This was the first Hep A vaccine patient has received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 05.08.2022
- Impfdatum
- 05.08.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Client received Hepatitis A vaccine #1 on 7/22/22. Client received dose #2 on 8/5/22. The second dose was administered too early. There was no reaction to the vaccine. Client was informed of the error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- Syphilis +, no symptoms
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 11.07.2022
- Impfdatum
- 11.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Adult publicly funded dose (1 mL) administered mistakenly instead of pediatric publicly funded dose (0.5 mL). No adverse reaction observed in clinic or reported by child or parents upon notification via telephone approximately 1 hour later. Parents and child notified. Primary care physician of patient notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- NKDA
- Vorherige Impfungen
- -