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Reporte zur Charge UT7411KA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

13Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 5 TN 2 KS 2 GA 2 KY 1 AL 1

VAERS 1880667

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE) · Charge UT7411KA

moderat
Staat
TN
Alter
16,0
Geschlecht
F
Eingang
04.12.2021
Impfdatum
17.11.2021
Beginn
17.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Chills Headache Hypertension Hypotension Nausea Pain Tachycardia Tremor Vomiting

Symptomtext

10/10 headache; Hypotensive; tachycardic; nausea and vomiting; nausea and vomiting; body shakes; shivers; hypertension; This is a spontaneous report from a contactable registered nurse. A 16 year-old female patient received meningococcal group b rlp2086 (TRUMENBA), administered in deltoid left, administration date 17Nov2021 12:09 (Lot number: ER2622, NDC number: 0005-0100-10, Expiration Date: Jan2024) at the age of 16 years as dose number unknown, 0.5 ml, single for immunisation; influenza vaccine (FLUZONE), intramuscular, administered in deltoid right, administration date 17Nov2021 (Lot number: UT7411KA, Expiration Date: 30Jun2022) as 0.5 ml, single; meningococcal vaccine a/c/y/w conj (dip tox) (MENACTRA), intramuscular, administered in deltoid right, administration date 17Nov2021 (Lot number: U7207AB, Expiration Date: 08Feb2023) as 0.5 ml, single. Relevant medical history included: "Asthma" (unspecified if ongoing). There were no concomitant medications. No prior vaccination within 4 weeks. No AE following prior vaccination. The following information was reported: HEADACHE (medically significant) with onset 17Nov2021, outcome "recovered" (Nov2021), described as "10/10 headache"; HYPOTENSION (medically significant) with onset 17Nov2021, outcome "recovered" (Nov2021), described as "Hypotensive"; TACHYCARDIA (medically significant) with onset 17Nov2021, outcome "recovered" (Nov2021), described as "tachycardic"; VOMITING (medically significant), NAUSEA (medically significant) all with onset 17Nov2021, outcome "recovered" (Nov2021) and all described as "nausea and vomiting"; TREMOR (non-serious) with onset 17Nov2021, outcome "recovered" (Nov2021), described as "body shakes"; CHILLS (non-serious) with onset 17Nov2021, outcome "recovered" (Nov2021), described as "shivers"; HYPERTENSION (non-serious) with onset 17Nov2021, outcome "recovered" (Nov2021), described as "hypertension". Within an hour of receiving the vaccines, the patient had a 10 out of 10 headache, body shakes, shivers, nausea. Around 1:30PM, the patients' mom was calling about this and then the patient was taken to the ER. The patient was hypotensive, tachycardic and had nausea and vomiting, also had hypertension. The patient received a bolus of IV fluids and IV benadryl. Symptoms eventually resolved. No relevant test. Clarified that the patient was not admitted to the hospital, she was just in the emergency room. It all had subsided but the reporting nurse did not know how long this lasted. Seriousness of 10 out of 10 headache, hypotensive, tachycardic, nausea and vomiting: the reporting nurse stated she did not know how to classify it, stating that if she had not gone to the ER, it would have been life threatening. She stated that it was definitely medically significant. The doctors in the office don't want to continue using this Lot number so the reporting nurse called their specific Rep regarding getting a replacement for the product and she was told that she would have to call the Safety department about that.; Sender's Comments: Based on a drug event temporal association and on the compatibility with the known adverse event profile of the suspect product, the company cannot completely exclude a reasonable possibility that the suspect vaccine meningococcal group b rlp2086 may have contributed to the onset of reported serious events including headache, hypotensive, tachycardic, nausea and vomiting all of which occurred within an hour of receiving the vaccines. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypotension
Hospital-Tage
-
Labordaten
Test Date: 20211117; Test Name: 10 out of 10 headache; Result Unstructured Data: Test Result:10/10
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Asthma
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1880667

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7411KA

moderat
Staat
TN
Alter
16,0
Geschlecht
F
Eingang
04.12.2021
Impfdatum
17.11.2021
Beginn
17.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Chills Headache Hypertension Hypotension Nausea Pain Tachycardia Tremor Vomiting

Symptomtext

10/10 headache; Hypotensive; tachycardic; nausea and vomiting; nausea and vomiting; body shakes; shivers; hypertension; This is a spontaneous report from a contactable registered nurse. A 16 year-old female patient received meningococcal group b rlp2086 (TRUMENBA), administered in deltoid left, administration date 17Nov2021 12:09 (Lot number: ER2622, NDC number: 0005-0100-10, Expiration Date: Jan2024) at the age of 16 years as dose number unknown, 0.5 ml, single for immunisation; influenza vaccine (FLUZONE), intramuscular, administered in deltoid right, administration date 17Nov2021 (Lot number: UT7411KA, Expiration Date: 30Jun2022) as 0.5 ml, single; meningococcal vaccine a/c/y/w conj (dip tox) (MENACTRA), intramuscular, administered in deltoid right, administration date 17Nov2021 (Lot number: U7207AB, Expiration Date: 08Feb2023) as 0.5 ml, single. Relevant medical history included: "Asthma" (unspecified if ongoing). There were no concomitant medications. No prior vaccination within 4 weeks. No AE following prior vaccination. The following information was reported: HEADACHE (medically significant) with onset 17Nov2021, outcome "recovered" (Nov2021), described as "10/10 headache"; HYPOTENSION (medically significant) with onset 17Nov2021, outcome "recovered" (Nov2021), described as "Hypotensive"; TACHYCARDIA (medically significant) with onset 17Nov2021, outcome "recovered" (Nov2021), described as "tachycardic"; VOMITING (medically significant), NAUSEA (medically significant) all with onset 17Nov2021, outcome "recovered" (Nov2021) and all described as "nausea and vomiting"; TREMOR (non-serious) with onset 17Nov2021, outcome "recovered" (Nov2021), described as "body shakes"; CHILLS (non-serious) with onset 17Nov2021, outcome "recovered" (Nov2021), described as "shivers"; HYPERTENSION (non-serious) with onset 17Nov2021, outcome "recovered" (Nov2021), described as "hypertension". Within an hour of receiving the vaccines, the patient had a 10 out of 10 headache, body shakes, shivers, nausea. Around 1:30PM, the patients' mom was calling about this and then the patient was taken to the ER. The patient was hypotensive, tachycardic and had nausea and vomiting, also had hypertension. The patient received a bolus of IV fluids and IV benadryl. Symptoms eventually resolved. No relevant test. Clarified that the patient was not admitted to the hospital, she was just in the emergency room. It all had subsided but the reporting nurse did not know how long this lasted. Seriousness of 10 out of 10 headache, hypotensive, tachycardic, nausea and vomiting: the reporting nurse stated she did not know how to classify it, stating that if she had not gone to the ER, it would have been life threatening. She stated that it was definitely medically significant. The doctors in the office don't want to continue using this Lot number so the reporting nurse called their specific Rep regarding getting a replacement for the product and she was told that she would have to call the Safety department about that.; Sender's Comments: Based on a drug event temporal association and on the compatibility with the known adverse event profile of the suspect product, the company cannot completely exclude a reasonable possibility that the suspect vaccine meningococcal group b rlp2086 may have contributed to the onset of reported serious events including headache, hypotensive, tachycardic, nausea and vomiting all of which occurred within an hour of receiving the vaccines. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypotension
Hospital-Tage
-
Labordaten
Test Date: 20211117; Test Name: 10 out of 10 headache; Result Unstructured Data: Test Result:10/10
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Asthma
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1840466

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7411KA

moderat
Staat
KS
Alter
61,0
Geschlecht
F
Eingang
03.11.2021
Impfdatum
03.11.2021
Beginn
03.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hypoaesthesia Paraesthesia

Symptomtext

Tingling and numbness in right arm and right side of face started on drive home from clinic approximately 1 hour after vaccine administration.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Asthma
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2621224

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7411KA

mild
Staat
TX
Alter
-
Geschlecht
F
Eingang
24.04.2023
Impfdatum
11.11.2021
Beginn
11.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain in extremity

Symptomtext

Pain after injection left deltoid

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Prenatal Vitamin
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1999428

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) · Charge UT7411KA

mild
Staat
KY
Alter
18,0
Geschlecht
F
Eingang
03.01.2022
Impfdatum
30.12.2021
Beginn
30.12.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Lymph node pain Lymphadenopathy

Symptomtext

Patient was seen in our office on 12/30/21 and given her flu vaccine and HPV vaccine. After leaving our office she went to Pharmacy and received her covid vaccine in the RA. After receiving that vaccine she developed a golfball size lymph node in her right underarm. Size of lymph node stayed the same but the location changed. The lymph node was very tender to the touch.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Lymph node pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1909465

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7411KA

mild
Staat
GA
Alter
24,0
Geschlecht
F
Eingang
30.11.2021
Impfdatum
12.11.2021
Beginn
13.11.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Influenza like illness Injection site pruritus

Symptomtext

Flu like symptoms, severe itching at injection site

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Immunocompromised
Andere Medikamente
Stelara, Actigall
Allergien
Zybox, Pipercylin
Vorherige Impfungen
1st Covid vaccine

VAERS 1904120

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7411KA

mild
Staat
TX
Alter
18,0
Geschlecht
M
Eingang
27.11.2021
Impfdatum
27.11.2021
Beginn
27.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site mass Swelling

Symptomtext

PT ADMINISTERED VACCINE IN THE LEFT ARM WITH A 25G 1" FLIPLOCK NEEDLE. THE PATIENT DEVELOPED A LUMP UNDERNEATH THE INJECTION SITE AFTER ADMINISTRATION. PT'S MOTHER IS A NURSE AND SHE MASSAGED THE AREA. THE PT ALSO APPLIED AN ICE BAG PROVIDED BY THE PHARMACY. DURING THE 15 MIN POST VACCINE WAIT PERIOD, THE SWELLING HAD MOSTLY RESOLVED AND PT SAID HE DID NOT HAVE ANY PAIN

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site mass
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1897939

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7411KA

mild
Staat
TX
Alter
4,0
Geschlecht
F
Eingang
24.11.2021
Impfdatum
22.11.2021
Beginn
22.11.2021
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema of eyelid Ocular hyperaemia Rash

Symptomtext

I finished the vaccination and immediately after that child developed redness under both eyes. I took Dr. to the room immediately and he examined the patient. She was acting fine except mild redness under both eyes and also in eyes. Dr. spoke to the patient's mother and explained to mother that we will keep her in office to observe her. Dr. then re-evaluated the patient after 30 minutes and the redness was almost gone. Dr. then discharged the patient and requested mother to give a call if any issues including any breathing complaints. Mother agreed. We spoke to Mother on 11/23/2021 and mother stated that the rashes are going away. I spoke to Mother on 11/24/2021 and per mother she only has a few red dots left on the eyes.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2364357

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7411KA

gering
Staat
KS
Alter
34,0
Geschlecht
F
Eingang
11.07.2022
Impfdatum
13.06.2022
Beginn
13.06.2022
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

Symptomtext

Varicella diluted w/expired Diluent.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Unknown
Allergien
None
Vorherige Impfungen
-

VAERS 2028035

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7411KA

gering
Staat
GA
Alter
0,4
Geschlecht
M
Eingang
12.01.2022
Impfdatum
09.12.2021
Beginn
12.01.2022
Tage bis Beginn
34,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product administered to patient of inappropriate age

Symptomtext

First dose was given at 5mo 16days of age. No adverse reactions.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1968070

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge ut7411ka

gering
Staat
TX
Alter
38,0
Geschlecht
M
Eingang
21.12.2021
Impfdatum
21.12.2021
Beginn
21.12.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Asthenia Fall

Symptomtext

Approx. 10 min after vaccines were given, while in waiting period in lobby, pt attempted to approach pharmacy window, pt faltered and fell. This happened at approx. 1:07 PM. 911 called, pt assisted on ground. Eventually helped to sitting position in chair. Pt given water and monitored until EMS arrived. EMS checked vitals/BP, and pt stable. Pt then declined EMS offer for further care/transport. Pt requested transport by pt agent/friend, who arrive ~25 min after incident. Pt states he has no PCP at this time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Asthenia
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
None reported
Vorgeschichte
None
Andere Medikamente
-
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1936410

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7411KA

gering
Staat
AL
Alter
49,0
Geschlecht
F
Eingang
09.12.2021
Impfdatum
11.11.2021
Beginn
11.11.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Wrong product administered

Symptomtext

Patient came in for a covid vaccination but was entered in the computer for a Flu vaccine and received a Flu shot instead of a Covid shot. No Adverse reactions occurred to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1877546

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7411KA

gering
Staat
TX
Alter
5,0
Geschlecht
M
Eingang
17.11.2021
Impfdatum
15.11.2021
Beginn
15.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered Syringe issue Wrong technique in product usage process

Symptomtext

When the vaccine was withdrawn from the thigh and plunger depressed to activate the self retracting needle, the medical assistant felt that 1/2 the vaccine squirted out. Another 0.1 mL was administered on the same visit.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-