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Reporte zur Charge U7920AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

9Reporte angezeigt
0Todesfaelle
2Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
FL 5 NE 1 ID 1 CO 1

VAERS 2724032

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U7920AA

schwer
Staat
NE
Alter
65,0
Geschlecht
M
Eingang
14.12.2023
Impfdatum
12.12.2023
Beginn
12.12.2023
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Cold sweat Dehydration Dizziness Hyperglycaemia Hypotension Hypothyroidism Laboratory test abnormal Loss of consciousness Pallor

Symptomtext

After receiving a Tetanus vaccination, the donor stated he was feeling faint. Donor was noted to be pale and clammy. Donor had an approximate 10 second loss of consciousness after which he was answering questions appropriately. Vital signs were obtained and donor was determined to bed hypotensive (69/44). Cold compressed was applied and the donor was given oral fluids. Vital signs were obtained again blood pressure was lower (50/35). The donor's legs were elevated, and donor continued to drink fluids. Vital signs were retaken and improved. Donor stated he only had a banana to eat prior to donating plasma. Donor stated he was feeling better, color returned and vital signs were within norma limits. Donor then stated he was feeling lightheaded again and could only see white light, stated he felt like he would pass out. Donor again had a loss of consciousness for approximately 10-15 seconds. Noted to be pale and clammy, blood pressure could not be read by machine. Decision was made to call EMS at 1241. Vital signs were attempted again and would not read. At 1246, vital signs were retaken and found to be very hypotensive (67/44). EMS arrived shorty after and assumed care.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
Tests were completed in the Emergency Room, results were not obtained by the plasmapheresis center. During a follow up, the Donor reported that the results showed hyperglycemia, hypothyroidism and dehydration.
Aktuelle Erkrankungen
The donor's wife reported that the donor had been ill with a cold since approximately December 4, 2023.
Vorgeschichte
None reported.
Andere Medikamente
None reported.
Allergien
No known allergies reported.
Vorherige Impfungen
-

VAERS 2722607

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U7920AA

schwer
Staat
FL
Alter
45,0
Geschlecht
M
Eingang
11.12.2023
Impfdatum
03.11.2023
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Guillain-Barre syndrome

Symptomtext

guillain barre syndrome; Initial information was received on 15-Nov-2023 regarding an unsolicited valid serious case received from a other health professional. This case is linked to case 2023SA359298(CLUSTER). This case involves 45 years old male patient who experienced guillain barre syndrome after receiving diphtheria-2/tetanus-5 adsorbed toxoids NO PRESERVATIVE ADULT [Tenivac]. The patient's past medical history, treatment(s), vaccination(s) and family history were not provided. Concomitant medications included measles vaccine, MUMPS VACCINE, rubella vaccine (MMR) for Immunisation; VARICELLA ZOSTER VACCINE (VARICELLA VACCINE) for Immunisation; and hepatitis b vaccine (HEP B VAX) for Immunisation. On 03-Nov-2023, the patient received a dose of 0.5 ml of suspect diphtheria-2/tetanus-5 adsorbed toxoids NO PRESERVATIVE ADULT (Suspension for injection) lot U7920AA, Expiry date :25-Oct-2025, strength was unknown via intramuscular route in unknown administration site for immunization. On an unknown date the patient developed guillain barre syndrome (guillain-barre syndrome) (unknown latency) following the administration of diphtheria-2/tetanus-5 adsorbed toxoids NO PRESERVATIVE ADULT. Action taken with DIPHTHERIA and TETANUS TOXOIDS (Tenivac) was not applicable. It was not reported if the patient received a corrective treatment for the event (guillain barre syndrome). At time of reporting, the outcome was Unknown for the event guillain barre syndrome. Seriousness criteria : This event was assessed as medically significant. The patient was hospitalized for this event. from 12-Nov-2023 Additional information was received on 01-Dec-2023 from : Case was upgraded from non case to valid. Texta mended accordingly.; Sender's Comments: Sanofi Company Comment dated 06-Dec-2023 : This case involves 45-year-old male patient who experienced guillain barre syndrome after receiving diphtheria-2/tetanus-5 adsorbed toxoids NO PRESERVATIVE ADULT [Tenivac].Further information regarding Past medical history, concurrent condition , allergic history, laboratory investigations excluding alternative etiologies for the reported events are needed to fully assess this case. Based upon the reported information, the role of a vaccine cannot be assessed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Guillain-Barre syndrome
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
MMR; VARICELLA VACCINE; HEP B VAX
Allergien
-
Vorherige Impfungen
-

VAERS 2716211

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U7920AA

schwer
Staat
FL
Alter
45,0
Geschlecht
M
Eingang
21.11.2023
Impfdatum
03.11.2023
Beginn
10.11.2023
Tage bis Beginn
7,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Guillain-Barre syndrome Intensive care

Symptomtext

Pt developed Guillain-Barr? syndrome

Weitere VAERSDATA-Felder
Praegender Schweregrund
Guillain-Barre syndrome
Hospital-Tage
8,0
Labordaten
Admitted to the ICU on 11/13/2023
Aktuelle Erkrankungen
Pt denied any illnesses at time of vaccination or 1 month before
Vorgeschichte
Pt denied any chronic health conditions.
Andere Medikamente
Pt denied taking medications
Allergien
Pt denied allergies
Vorherige Impfungen
-

VAERS 2725858

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U7920AA

moderat
Staat
-
Alter
49,0
Geschlecht
F
Eingang
20.12.2023
Impfdatum
31.10.2023
Beginn
31.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthropathy Bone marrow oedema Discomfort Immediate post-injection reaction Loss of personal independence in daily activities Magnetic resonance imaging abnormal Mobility decreased Pain Sleep disorder Tendon disorder Tendon rupture

Symptomtext

Td given in left upper deltoid, Hep A given left lower deltoid. "Uncomfortableness immediately after injection" Arm sore for the remainder of the day. Following day, the pain was "horrible." Difficulty lifting arm, unable to exercise d/t the discomfort, sleep issues, MRI ordered and completed. Orthopedic consult pending

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
MRI shoulder WO con on 12/12/2023. Mild tendinosis of the distal infraspinatus tendon without full-thickness tear Mild subchondral marrow edema of the posterior humeral head. This can be associated with the posterior impingement, but the possibility of a bone bruise is also raised. Mild hypertrophic changes of the acromioclavicular joint
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2728569

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U7920AA

mild
Staat
FL
Alter
60,0
Geschlecht
M
Eingang
29.12.2023
Impfdatum
29.11.2023
Beginn
30.11.2023
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Back pain Chills Influenza like illness Myalgia Nausea Secretion discharge

Symptomtext

Donor stated having severe muscle pain all down the right arm following his last tetanus shot. The pain then moved from his right arm to the entire back. Donor also reported nausea, heavy mucous, chills and severe flu like symptoms without fever. Donor stated his symptoms started the day after his shot and lasted approximately four days with severe symptoms and 4 days with symptoms tapering off. Donor reported his symptoms approximately 10 days after symptoms had been resolved.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Back pain
Hospital-Tage
-
Labordaten
None reported.
Aktuelle Erkrankungen
None reported.
Vorgeschichte
None reported.
Andere Medikamente
Donor reported taking OTC - ASA 81MG - IBUPROFEN.
Allergien
None reported.
Vorherige Impfungen
-

VAERS 2725427

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U7920AA

mild
Staat
ID
Alter
62,0
Geschlecht
F
Eingang
19.12.2023
Impfdatum
25.11.2023
Beginn
26.11.2023
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Diarrhoea Influenza like illness Injection site pain Injection site warmth Lymphadenopathy Nausea Pain Pain in extremity Pyrexia

Symptomtext

Significant arm soreness, body aches, subjective fever, swollen lymph nodes in the armpit, and soreness with warmth around the area of the injection. Nausea with diarrhea. Provided Zofran on 11/27/2023. As of 12/19/2023 patient has arm soreness at the injection site and lymph nodes continue to be about 10% swollen. No longer has flu-like symptoms.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Diarrhoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Estradiol 0.01% cream, Flovent HFA 110 MCG Inhaler, Fluoxetine HCL 10mg capsule, Fluoxetine HCL 20mg capsule, Icosapent Ethyl 1 gram capsule, Metformin HCL ER 500mg tablet, Omeprazole DR 20mg capsule
Allergien
Azithromycin, Sulfonamide Antibiotics
Vorherige Impfungen
-

VAERS 2724458

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U7920AA

mild
Staat
CO
Alter
24,0
Geschlecht
F
Eingang
15.12.2023
Impfdatum
14.12.2023
Beginn
15.12.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Induration Lip swelling Pruritus Rash

Symptomtext

patient contacted Immunization clinic program assistant (who interpreted the phone call from patient) to RN. Patient states that on Friday, December 15, 2023 pt started experiencing potential reactions post vaccinations (vaccinations received yesterday around 1:35PM on Thursday December 14, 2023). Patient reports at around 10:00AM on Friday, December 15, 2023, pt was experiencing a rash to her shoulders and arms, redness to the face, itching of the neck (Interpreting program assistant verified that patient did NOT have itching or swelling in her throat), and patient had a swollen and hardened top upper lip. Program assistant verified with patient, on the phone, that the patient was NOT having any difficulty swallowing, breathing, or speaking. RN instructed pt to seek immediate medical attention, by going to the Emergency Room/Urgent Care Immediately, so that she may get help and potential treatment. Program assistant interpreted this strong recommendation and encouragement to the patient on the phone. Patient verbalized understanding to RN's recommendation to seek immediate medical attention. At this time patient has not contacted clinic back to discuss outcomes or treatment.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
Patient verbally denied any known illnesses at the time of vaccination
Vorgeschichte
Patient verbally denied having any chronic or long-standing health conditions at the time of vaccination.
Andere Medikamente
Patient verbally denied taking any medications or supplements at the time of vaccination
Allergien
Patient verbally denied any known allergies to foods, medications, latex, or past immunizations
Vorherige Impfungen
-

VAERS 2707947

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U7920AA

mild
Staat
FL
Alter
36,0
Geschlecht
M
Eingang
31.10.2023
Impfdatum
31.10.2023
Beginn
31.10.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extremity contracture Malaise Muscle rigidity

Symptomtext

Patient here for lab follow up and vaccines. Patient has history of seizures. Last seizure over two years ago. NP on call made aware of patient history and stated it is ok to vaccinate patient today. Td and MMR administered to patient. Patient stated he did not feel well after the vaccines were administered and put his head down and leaned over into his lap. Patient became rigid and arms and legs contracted and extended. He was lowered safely to the floor by two RNs. Patients head kept safe. Episode lasted approximately 30 seconds. Patient sustained no injuries. Patient sat up and had normal mental status, drank water, and had reactive pupils. Prior to episode, patient denied reactions to vaccines and faiting when getting vaccines. He stated that he had recieved many vaccines with no issues. After episode on 10/31/23, patient reported that he had fainted the last time he had his blood drawn. Patient able to hold conversation and reply appropriately. Vital signs re-checked. BP 133/90 HR 70. Patient advised not to drive. Patient insisted upon leaving clinic and stated "I am fine." Left ambulatory escorted by RN to exit window. No distress noted.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Malaise
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Patient denies
Vorgeschichte
Seizures. Patient reported being seizure free for over two years.
Andere Medikamente
Patient denies
Allergien
NKA
Vorherige Impfungen
-

VAERS 2712661

SANOFI PASTEUR · TD ADSORBED (NO BRAND NAME) · Charge U7920AA

gering
Staat
FL
Alter
37,0
Geschlecht
F
Eingang
10.11.2023
Impfdatum
07.11.2023
Beginn
08.11.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Vaccination site erythema Vaccination site induration Vaccination site swelling

Symptomtext

Redness, swelling, and induration over the left deltoid area where the vaccine was administered.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vaccination site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Laceration to left lower leg, lumbar strain
Vorgeschichte
None
Andere Medikamente
Ibuprofen, Robaxin, Medrol Dospak
Allergien
No known allergies
Vorherige Impfungen
-