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Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

17Reporte angezeigt
1Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MN 7 MI 2 PA 2 SD 1 NJ 1 NY 1 VA 1

VAERS 2131433

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT7336NA

kritisch
Staat
-
Alter
58,0
Geschlecht
M
Eingang
22.02.2022
Impfdatum
29.09.2021
Beginn
10.10.2021
Tage bis Beginn
11,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Cardioversion Gastrointestinal tube insertion Hypothermia Hypoxia Intensive care Postoperative adhesion Respiratory arrest Respiratory distress Resuscitation Small intestinal obstruction

Symptomtext

Small bowel obstruction due to postoperative adhesions. Patient developed increased respiratory distress after multiple NG tube placement attempts, he then developed hypoxia and respiratory arrest. Patient received 15 minutes of CPR, 4 doses of epinephrine, and 2 doses of bicarbonate, and 1 cardioversion. Patient initially required ICU support along with a hypothermic protocol and 3 pressor support. Patient slowly stabilized and hypothermia reversal began and support was slowly weaned. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Respiratory arrest
Hospital-Tage
12,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1936333

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

kritisch
Staat
SD
Alter
-
Geschlecht
M
Eingang
28.01.2022
Impfdatum
08.11.2021
Beginn
01.11.2021
Tage bis Beginn
-
Dosis
1
Route/Site
IM / UN
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arrhythmia Body temperature Body temperature increased Carbon dioxide Fatigue Autopsy Brain oedema Condition aggravated Death Myalgia Oropharyngeal pain Tachycardia Giant cell arteritis Hypersomnia Impaired work ability Inflammation Malaise Heart rate

Symptomtext

Death From Myocarditis; fatal arrhythmia that killed him instantly; increased heart rate; Tachycardia; temperature was up to 100.2; fatigue; muscle soreness; sore throat; Product use for unapproved combination; left ventricular dysfunction; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. Other Case identifier(s): US-PFIZER INC-202200065467 (Pfizer), US-PFIZER INC-202200142396 (pfizer). A 26 year-old male patient received bnt162b2 (BNT162B2), administration date 08Nov2021 (Lot number: FE3590) as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), administration date 08Nov2021 (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Pfizer 1st dose - ER8733), administration date: 26Mar2021, for COVID-19 Immunization; Bnt162b2 (Pfizer 2nd dose - EW0164), administration date: 16Apr2021, for COVID-19 immunisation. The following information was reported: MYOCARDITIS (death, medically significant) with onset 12Nov2021, outcome "fatal", described as "Death From Myocarditis"; ARRHYTHMIA (death) with onset 12Nov2021, outcome "fatal", described as "fatal arrhythmia that killed him instantly"; LEFT VENTRICULAR DYSFUNCTION (death) with onset Nov2021, outcome "fatal", described as "left ventricular dysfunction"; FATIGUE (non-serious) with onset 11Nov2021, outcome "not recovered", described as "fatigue"; MYALGIA (non-serious) with onset 11Nov2021, outcome "not recovered", described as "muscle soreness"; OROPHARYNGEAL PAIN (non-serious) with onset 11Nov2021, outcome "recovered" (2021), described as "sore throat"; HEART RATE INCREASED (non-serious) with onset 12Nov2021, outcome "not recovered", described as "increased heart rate"; TACHYCARDIA (non-serious) with onset 12Nov2021, outcome "unknown", described as "Tachycardia"; BODY TEMPERATURE INCREASED (non-serious) with onset 12Nov2021, outcome "recovered" (12Nov2021 16:30), described as "temperature was up to 100.2"; PRODUCT USE ISSUE (non-serious) with onset 08Nov2021, outcome "unknown", described as "Product use for unapproved combination". The patient underwent the following laboratory tests and procedures: body temperature: (unspecified date) 100.2 Fahrenheit, notes: his temperature was up to 100.2; carbon dioxide (0.0-1.5): (unspecified date) 0.2 %, notes: Normal; heart rate: (unspecified date) 112, notes: his heart rate was elevated to 112; (10Nov2021) 97; (10Nov2021) 85; (10Nov2021) 91; (10Nov2021) 84; (10Nov2021) 91; (10Nov2021) 89; (10Nov2021) 90; (10Nov2021) 89; (10Nov2021) 84; (10Nov2021) 85; (10Nov2021) 98; (10Nov2021) 89; (11Nov2021) 90; (11Nov2021) 120; (11Nov2021) 119; (11Nov2021) 120; (11Nov2021) 121; (11Nov2021) 127; (11Nov2021) 126; (11Nov2021) 127; (11Nov2021) 131; (11Nov2021) 128; (11Nov2021) 131; (11Nov2021) 130; (11Nov2021) 130; (11Nov2021) 128; (12Nov2021) 123; (12Nov2021) 127; (12Nov2021) 128; (12Nov2021) 135; (12Nov2021) 74; (12Nov2021) 141; (12Nov2021) 71; (12Nov2021) 146; (12Nov2021) 144; (12Nov2021) 138; (12Nov2021) 149; (12Nov2021) 148; (12Nov2021) 145; (12Nov2021) 63; (12Nov2021) 63; (12Nov2021) 119; (12Nov2021) 68; (12Nov2021) 64; (12Nov2021) 64; (12Nov2021) 64; (12Nov2021) 65; (12Nov2021) 67; (12Nov2021) 67; (12Nov2021) 67; (12Nov2021) 66; (12Nov2021) 66; (12Nov2021) 66; oxygen saturation: (unspecified date) 100 %, notes: his oxygen was at 100%. Therapeutic measures were taken as a result of oropharyngeal pain, body temperature increased. The patient date of death was 12Nov2021. The reported cause of death was myocarditis, arrhythmia, left ventricular dysfunction. Clinical course was reported as, a 26-year old (Place) man who died 12Nov2021, of myocarditis- four days after his booster dose Of Pfizer's Covid vaccine- had no idea he was experiencing a rare and supposedly "mild" heart problem after the shot. (Name) only warning signs were fatigue, muscle soreness and an increased heart rate, family members said. Reported that the pathologist performed scans of patient's heart and gathered 22 slides which confirmed that # had severe myocarditis from the Pfizer booster vaccine that led to his death. In an exclusive interview With (Show name), (Name)'s father, mother and sister said the Centers for Disease Control and Prevention (CDC) has not investigated (Name)'s death, The CDC also did not contact the pathologist who performed the autopsy or request the documents which confirmed (Name)'s death was caused by the Pfizer vaccine. According to the autopsy report and certificate of death, (Name) died from severe heart damage from "myocarditis in the left ventricle due to the recent Pfizer COVID-19 booster vaccine." (Name)'s mother, (Name), said her son was pro-vaccine and worked in an environment where he needed to be vaccinated. According to (Name)'s vaccination cards, he received his first Pfizer shot on 26Mar2021, and the second dose on 16Apr2021. (Name) said her son, who didn't experience any negative adverse events after the first two doses, received a third booster dose on 08Nov2021. "This was on a Monday," (Name) said. "Tuesday and Wednesday he was fine, but Thursday morning- 72 hours after the booster- he called and said he had a sore throat." (Name) made her son some hot apple cider and he took throat lozenges and went to work, but within two hours he called her to pick him up because he was so fatigued he couldn't work. When (Name) asked him what was wrong, (Name) told her he had some muscle soreness, exhaustion and a sore throat. 'When we searched, what are your reactions to having the Pfizer vaccine,' a lot of the results say people deal with fatigue, muscle soreness and everything, so we both just brushed it Off as reactions to the vaccine and it was no big deal," (Name) said. (Name) slept through Thursday. On Friday morning, he told his mother he would have to call into work again because he was too exhausted to go in. (Name) visited (Name)and said he appeared to be normal, other than fatigue and muscle soreness. "He wasn't really acting sick, just exhausted," she said. (Name), a critical care nurse Of 35 years, took her son's vitals and noted his temperature was up to 100.2 and his heart rate was elevated to 1 12. She thought it was related to the fever, so she gave him Tylenol. Later that day, (Name) texted his mother that his fever was down. By 4:30 p.m., his oxygen was at 100%, but his heart rate was still elevated. (Name)'s father, (Name), visited his son around 5 p.m. and they had dinner. He left at 6 p.m. Two hours later their son was dead. The family knows when (Name) died because of the fitness watch data they retrieved from his phone. (Name) had an app enabled that measured his heart rate up to the time of his death. (Name) said: "He went to sit down in his recliner and when we (the family) came the next day we were able to pull up the data from his fitness watch showing the exact time Of his death and exactly What his heart rate was doing the past two hours. "It showed he was beating at IOOs all during the day and after 6 p.m., when he sat in the recliner, his heart rate dropped into the 60s, which was low for (Name), Who always had a resting heart rate in the 80s and 90s - and then it just stopped." (Name) said When they found (Name) the next morning, there were no signs he knew he was going to die. "He was even having a two-way conversation with several of his friends before his death. The phone and remote control were on his lap," his mother said. The family called # and detectives came to make sure it wasn't a crime scene because "26-year-olds don't just die," (Name) said. When detectives separated (Name) and her husband for questioning, she told the detectives the only thing she knew was that four days prior her son had received Pfizer's vaccine and he was having adverse reactions. Four davs later he was dead. Autopsy confirms (Name) died of myocarditis After (Name) died, an autopsy had to be performed to confirm the cause of death. "When they first did the preliminaries they couldn't find anything - his heart looked normal," (Name) said. But "the pathologist said he was going to do 22 different slides to see what he could find." Meanwhile, (Name) said she started hearing stories about young males getting myocarditis from Covid vaccines. "I knew Covid could cause MIS-C (multisystem inflammatory syndrome), but nobody told me the vaccine was giving people myocarditis," (Name) said. "There's a big difference between Covid giving you myocarditis and a vaccine giving you myocarditis and actually killing you." (Name) said: When the pathologist looked at the 22 segments of (Name)'s heart, it showed the vaccine inflamed and attacked his entire heart. There was so much damage to the heart. It was full multi-focal myocarditis, and it wasn't just affecting one part of his heart, it was attacking his whole septum and ventricles." (Name) thinks her son developed so much inflammation from the booster that his heart developed a fatal arrhythmia that killed him instantly. She spoke with several cardiologists who were surprised her son never experienced any type of chest pain. "The hallmark signs as a parent that would prompt you to seek medical help were not given to me," (Name) said. "He didn't know his heart was racing, or fluttering or becoming A-fib. All he complained about was the muscle soreness and fatigue." (Name)'s private physician called the family after his autopsy results were back and told (Name) if she would have called him and informed him Of (Name)'s symptoms, he would have said it was just a side effect of the vaccine. "If we would have brought him in Thursday or Friday, nobody would have discovered it," (Name) said. (Name)'s sister, (Name), said, "My brother felt he wasn't bad enough to seek medical attention because he wasn't having any symptoms, it just came out Of nowhere." "That's What is so amazing that he didn't have any chest pain, he didn't feel his heart flutter, he didn't have any shortness of breath," (Name) said. "l mean two hours before he died he has 100 percent oxygen concentration. It just didn't show anything outside of an elevated heart rate." (Name) said she took a full set of vitals and her son just didn't feel sick. 'When you're sick, you're in bed, but he just never felt that way. He just got into a rate the heart couldn't keep up with and he died (Name) said she is thankful an autopsy was performed because it revealed her son died directly from the vaccine and the myocarditis he suffered was from the vaccine. "It's documented proof," (Name) said. "He died directly from the Pfizer booster." CDC ignores reports of death caused by myocarditis Both (Name)'s family and the pathologist submitted a report to the Vaccine Adverse Event Reporting System (VAERS), but to this day, neither have been contacted by the CDC about (Name)'s death. "You would think the death Of a child from a reaction to a Covid vaccine that's documented on the death certificate and autopsy, the CDC would have reached out to us immediately," (Name) said. "You would think the CDC would have called the pathologist." According to the CDC website, the agency contacts people who meet the case definition for myocarditis following mRNA Covid vaccine and have submitted a report to VAERS. To meet the case definition, people must have had "symptoms such as chest pain, shortness Of breath and feelings of having a fast-beating, fluttering or pounding heart, and medical tests to support the diagnosis of myocarditis and rule out other causes." This rules out deaths like (Name), Who wasn't diagnosed With myocarditis prior to death and did not experience the symptoms that would normally fall under the CDCs case definition. The CDC website does not State What happens to these cases, but there is no indication they are tracked or included in the CDC's myocarditis numbers. (Name) said the state's health department also has not investigated her son's death, as they said they first needed to be contacted by the CDC. "Nobody wants to touch it," He said. "I've been calling the health department the last few days and they keep saying they have to wait for the CDC and the facts. I told them the facts are in the autopsy, but they said they had to wait longer." (Name) said: We've heard no response. We contacted the local news station to get the word out that this happened, and they said their hands were tied_ We called the pathologist, no comment. The governor, no comment. The health department, no comment. The CDC, no comment. So, nobody's talking about it." (Name) said her main goal in sharing her son's story is to let other families know this happened Without any warning. "Thirty-five years as a registered nurse, I should have known something was happening and I didn't know," she said. "There were no signs." (Name) said: "It's sad because it's like (Name) death never occurred. I just don't get why we can't warn parents that something like this ? to watch out. He didn't have any symptoms the first two days and then he developed symptoms the third day. But I didn't put it together because he didn't have the symptoms where you think something was destroying his heart. But he was dead at four days. "(Name) been gone for two months and nobody knows that this boy gave his life for the greater good to get a booster." (Name) said he doesn't feel like anybody wants to deal With the people Who get sick or die following COVID vaccines. (Name) said her son was an innocent 26-year-old who was "doing everything right" by getting his vaccines and booster, but then died - and nobody wants to acknowledge it, accept it or tell her why. The family of 26-year-old (Name) is still grieving after a Pfizer Covid-19 vaccine booster jab led to his untimely death from myocarditis last November. The (Place) man's official exclusively obtained by the Health Defense, shows he suffered "multifocal myocarditis" just days following his third dose of the experimental mRNA shot, which his family said was required by his occupation. (Name) made her son some hot apple cider and he took throat lozenges and went to work, but within two hours he called her to pick him up because he was so fatigued he couldn't work. When (Name) asked him what was wrong, (Name) told her he had some muscle soreness, exhaustion and a sore throat. (Name) slept through Thursday. On Friday morning, he told his mother he would have to call into work again because he was too exhausted to go in. (Name) visited (Name) and said he appeared to be normal, other than fatigue and muscle soreness. "He wasn't really acting sick, just exhausted, " she said. (Name), a critical care nurse of 35 years, took her son's vitals and noted his temperature was up to 100.2 and his heart rate was elevated to 112. She thought it was related to the fever, so she gave him Tylenol. Later that day, (Name) texted his mother that his fever was down. By 4:30 p.m., his oxygen was at 100%, but his heart rate was still elevated. (Name) father, (Name), visited his son around 5 p.m. and they had dinner. He left at 6 p.m. Two hours later their son was dead. The autopsy report notes (Name) fitness watch recorded an extremely high heart rate the morning of his death: "His fitness watch recorded no cardia activity after 1959 hours. He did not respond to a text at 21:00 hours. On 13Nov he did not text his mother in the morning as he usually did and his family subsequently found him deceased in his recliner. " A death certificate issued by the State of (state name) and obtained by the (Show name) lists (Name) cause of death from "multifocal myocarditis involving the left ventricle and septum," with a second cause of death listed as "Recent Pfizer Covid-19 booster vaccine."Certificate of Death Place of death Information: Type: Decedent's Home Cause of Death Part I: Multifocal myocarditis involving the left ventricle and septum. Part II: Recent Pfizer Covid booster vaccine Coroner Contacted: Yes Autopsy Performed: Yes Autopsy Available: Y Manner of Death: Natural Causes (Name) mother says she's glad they authorized an autopsy as it's definitive proof the vaccine was what caused her son's death. "It's documented proof," (Name) told the (show name). "He died directly from the Pfizer booster." The family says despite the surprising nature of (Name) death and official documents, they have yet to be contacted by the CDC, the FDA or any other federal health agency about his death. "You would think the death of a child from a reaction to a Covid vaccine that's documented on the death certificate and autopsy, the CDC would have reached out to us immediately," (Name) bemoaned. "You would think the CDC would have called the pathologist." She added: "We've heard no response. We contacted the local news station to get the word out that this happened, and they said their hands were tied. We called the pathologist, no comment. The governor, no comment. The health department, no comment. The CDC, no comment. So, nobody s talking about it." The family is now seeking justice for their son by warning others of the potentially deadly consequences of receiving the jabs, which can evidently manifest with little, or no symptoms. "l want answers and I want Pfizer and the CDC to call me and tell me what went wrong. I want to save another child," a bereaved (Name) insists. However, this wasn't an issue for (Name), who his family described as pro-vaccine. (Name) CDC vaccine card documents his first and second doses of Pfizer's experimental gene therapy on 26Mar, and 16Apr2021, respectively. "Tuesday and Wednesday he was fine," described (Name) mother, (Name), "but Thursday morning 72 hours after the booster - he called and said he had a sore throat." The Defended s (Name) reports on how the family had no indications (Name) heart would soon fail, and believed he was experiencing mild side effects. This 26-year-old withheld male was discovered sitting in his recliner at home, He has a history Of a Of Galen malformation with multiple therapies. He had received his third Pfizer Covid shot booster and flu shot on 08Nov2021. On morning Of 11Nov, he complained of sore throat and fatigue. On morning of 12Nov2021, his apple watch recorded tachycardia. Later in the day. he had complained muscle aches and sore throat with a temperature Of 1002 F. The examination was conducted 15Nov2021 at 0915 hours. Autopsy information was reported as: Specimen: Body, General Information: Age: 26, Sex: M, Length: 69 inches, Weight: 240 pounds, Date of Death 12Nov2021, Date of autopsy: 15Nov2021; Final Diagnosis: Multifocal myocarditis involving the cardiac left ventricle and interventricular septum A. Received Pfizer Covid booster shot and flu shot on 08Nov2021 B. Pulmonary congestion C. Splenomegaly D. Cerebral edema; Il. Right cardiac ventricle; III. Vein of Galen malformation. clinical A. Multiple vessels Of varying size with refractile foreign material with giant cell inflammatory response and calcification; large caliber vessel with thrombus. Cause of death: Multifocal myocarditis involving the left ventricle and septum. Contributory: Recent Pfizer Covid booster vaccine Manner of death: Normal/Natural. Comment: Myocarditis following administration of pfizer Covid vaccine has been noted in male patients between ages of 16 and 29 Years, and most commonly presents 3 to 5 days following administration. Post Pfizer Covid vaccination myocarditis has been identified to cause left ventricle dysfunction.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200082021 Pfizer; Reported Cause(s) of Death: Death From Myocarditis; fatal arrhythmia that killed him instantly; left ventricular dysfunction

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
Test Name: Body temperature; Result Unstructured Data: Test Result:100.2 Fahrenheit; Comments: his temperature was up to 100.2; Test Name: CO2; Test Result: 0.2 %; Comments: Normal; Test Name: Heart rate; Result Unstructured Data: Test Result:112; Comments: his heart rate was elevated to 112; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:97; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:85; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:91; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:84; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:91; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:89; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:90; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:89; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:84; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:85; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:98; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:89; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:90; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:120; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:119; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:120; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:121; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:127; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:126; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:127; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:131; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:128; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:131; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:130; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:130; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:128; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:123; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:127; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:128; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:135; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:74; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:141; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:71; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:146; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:144; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:138; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:149; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:148; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:145; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:63; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:63; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:119; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:68; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:64; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:64; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:64; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:65; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:67; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:67; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:67; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:66; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:66; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:66; Test Name: Oxygen level; Test Result: 100 %; Comments: his oxygen was at 100%
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1854240

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

schwer
Staat
NJ
Alter
16,0
Geschlecht
M
Eingang
09.11.2021
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: ja
Feeling abnormal Pallor Seizure

Symptomtext

About 10 minutes after immunizations administered patient was standing at check out and told mom he didn't feel right. He sat down on bench and mom reports patient convulsed, b/l arms and head x2 for about 3-5 seconds. Patient thinks he may have blacked out momentarily, but recalls full event. Patient then reported he felt normal, but appeared pale. He stayed in lying position for at least 5 minutes with cool compress to forehead/neck, patient's coloring returned to normal. He then sat for 10 minutes, drank 2 cups of water continued to report he felt fine. Denies headache, dizziness, lightheadedness or ringing in ear. HR was 60 bpm, RRR. Patient walked around waiting area, felt fine and left the office with mom. Reviewed with mom concerns to monitor for.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Amoxicillin - Hives
Vorherige Impfungen
-

VAERS 1848851

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

schwer
Staat
MN
Alter
8,0
Geschlecht
F
Eingang
06.11.2021
Impfdatum
06.11.2021
Beginn
06.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syncope Vomiting

Symptomtext

Syncopal episode with subsequent emesis

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
Vital signs only.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Multivitamin
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2457508

UNKNOWN MANUFACTURER · INFLUENZA (SEASONAL) (NO BRAND NAME) · Charge UT7336NA

moderat
Staat
MN
Alter
7,0
Geschlecht
M
Eingang
24.09.2022
Impfdatum
06.11.2019
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Condition aggravated Device connection issue Seasonal allergy Underdose Urticaria

Symptomtext

hives and urticaria on his arms (urticaria); seasonal allergic rhinitis due to pollen and drug allergies; hives turned and got much worse on his face, trunk, arms and legs; the liquid leaked outside of the syringe and onto his arm and then onto the floor. They are not sure if the patient received the full dose of the vaccine or not; e liquid leaked outside of the syringe and onto his arm and then onto the floor. They are not sure if the patient received the full dose of the vaccine or not; This spontaneous case was reported by an other health care professional and describes the occurrence of URTICARIA (hives and urticaria on his arms (urticaria)), SEASONAL ALLERGY (seasonal allergic rhinitis due to pollen and drug allergies) and CONDITION AGGRAVATED (hives turned and got much worse on his face, trunk, arms and legs) in a 7-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. FK5127) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product INFLUENZA VACCINE for Prophylactic. Previously administered products included for Drug use for unknown indication: cefdinir and amoxicillin allergy (and the reaction is hives). Past adverse reactions to the above products included Rash with cefdinir; and Serum sickness with amoxicillin allergy. Concurrent medical conditions included Bronchial hyperreactivity since 06-Nov-2019, Reactive airways disease since 06-Nov-2019 and Asthma (He is using the ProAir Proventil inhaler). Concomitant products included SALBUTAMOL (PROVENTIL [SALBUTAMOL]) for an unknown indication. On 06-Nov-2019, the patient received dose of INFLUENZA VACCINE (unknown route) 1 dosage form. On 05-Nov-2021, received dose of INFLUENZA VACCINE (unknown route) dosage was changed to 1 dosage form. On 26-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced URTICARIA (hives and urticaria on his arms (urticaria)), SEASONAL ALLERGY (seasonal allergic rhinitis due to pollen and drug allergies) (seriousness criterion medically significant), CONDITION AGGRAVATED (hives turned and got much worse on his face, trunk, arms and legs) (seriousness criterion medically significant), DEVICE CONNECTION ISSUE (the liquid leaked outside of the syringe and onto his arm and then onto the floor. They are not sure if the patient received the full dose of the vaccine or not) and UNDERDOSE (e liquid leaked outside of the syringe and onto his arm and then onto the floor. They are not sure if the patient received the full dose of the vaccine or not). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for Hives, at an unspecified dose and frequency. At the time of the report, URTICARIA (hives and urticaria on his arms (urticaria)) had not resolved, SEASONAL ALLERGY (seasonal allergic rhinitis due to pollen and drug allergies), DEVICE CONNECTION ISSUE (the liquid leaked outside of the syringe and onto his arm and then onto the floor. They are not sure if the patient received the full dose of the vaccine or not) and UNDERDOSE (e liquid leaked outside of the syringe and onto his arm and then onto the floor. They are not sure if the patient received the full dose of the vaccine or not) outcome was unknown and CONDITION AGGRAVATED (hives turned and got much worse on his face, trunk, arms and legs) was resolving. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. This case was identified as part of a retrospective clean-up activity where certain emails received in the Moderna mailbox were missed to be booked-in Turned and got much worse on his face, trunk, arms and legs then the mother gave him antihistamines and took him to the emergency room at that time. It all improved with antihistamines and there were no systemic issues present. 11. He has multiple aero. Company comment This spontaneous case reported by a Health Care Professional, concerns a 7 year old male child, , with relevant concurrent illness of Bronchial hyperreactivity, Reactive airways disease and Asthma, who experienced the unexpected, serious (medically significant) events of URTICARIA (hives and urticaria on his arms (urticaria)), SEASONAL ALLERGY (seasonal allergic rhinitis due to pollen and drug allergies) and CONDITION AGGRAVATED (hives turned and got much worse on his face, trunk, arms and legs) unknown days after receiving a dose of mRNA-1273 vaccine in the covid 19 vaccination series, along with other non serious events. It was reported that the vaccine liquid leaked outside of the syringe and onto his arm and then onto the floor. They were not sure if the patient received the full dose of the vaccine or not. Previous adverse reactions of the patient included Rash with cefdinir; and Serum sickness with amoxicillin. Patient had previously received 2 doses with Influenza vaccines with the last dose given about 20 days prior to receiving Moderna vaccine, which are all confounders to the events. The patient was treated with Diphenhydramine hydrochloride for Hives. No further clinical information on other comorbidities, labs, diagnostics, were reported. The event urticaria had not resolved, condition aggravated was resolving and outcome of Seasonal allergy was unknown. The benefit-risk relationship of mRNA- 1273 vaccine is not affected by this report.; Sender's Comments: This spontaneous case reported by a Health Care Professional, concerns a 7 year old male child, , with relevant concurrent illness of Bronchial hyperreactivity, Reactive airways disease and Asthma, who experienced the unexpected, serious (medically significant) events of URTICARIA (hives and urticaria on his arms (urticaria)), SEASONAL ALLERGY (seasonal allergic rhinitis due to pollen and drug allergies) and CONDITION AGGRAVATED (hives turned and got much worse on his face, trunk, arms and legs) unknown days after receiving a dose of mRNA-1273 vaccine in the covid 19 vaccination series, along with other non serious events. It was reported that the vaccine liquid leaked outside of the syringe and onto his arm and then onto the floor. They were not sure if the patient received the full dose of the vaccine or not. Previous adverse reactions of the patient included Rash with cefdinir; and Serum sickness with amoxicillin. Patient had previously received 2 doses with Influenza vaccines with the last dose given about 20 days prior to receiving Moderna vaccine, which are all confounders to the events. The patient was treated with Diphenhydramine hydrochloride for Hives. No further clinical information on other comorbidities, labs, diagnostics, were reported. The event urticaria had not resolved, condition aggravated was resolving and outcome of Seasonal allergy was unknown. The benefit-risk relationship of mRNA- 1273 vaccine is not affected by this report.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Asthma (He is using the ProAir Proventil inhaler); Bronchial hyperreactivity; Reactive airways disease
Vorgeschichte
-
Andere Medikamente
PROVENTIL [SALBUTAMOL]
Allergien
-
Vorherige Impfungen
-

VAERS 1947209

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

moderat
Staat
MN
Alter
5,0
Geschlecht
M
Eingang
14.12.2021
Impfdatum
06.11.2019
Beginn
26.11.2021
Tage bis Beginn
751,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Condition aggravated Seasonal allergy Urticaria

Symptomtext

urticaria on his arms; hives turned and got much worse on his face, trunk, arms and legs; seasonal allergic rhinitis due to pollen and drug allergies; Initial information received on 02-Dec-2021 regarding an unsolicited valid serious case received from an other health professional. This case involves a 7 years old male patient (height: 127 cm and weight: 23 kg) who had hives and urticaria on his arms (urticaria), hives turned and got much worse on his face, trunk, arms and legs (condition aggravated) and seasonal allergic rhinitis due to pollen and drug allergies (seasonal allergy) after receiving INFLUENZA VACCINE and COVID-19 VACCINE MRNA. The patient's medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included SALBUTAMOL (PROVENTIL [SALBUTAMOL]). It was unknown if the patient had any additional medical history, concomitant disease or risk factor. At the time of the event, the patient had ongoing Reactive airways disease on 06-NOV-2019 and Drug allergy with amoxicillin and cefdinir. the amoxicillin says serum sickness and the reaction is hives and the reaction to cefdinir is a rash. The patient is using inhalers and it is originally reported that he has asthma because she sees that there is an asthma action plan in his chart. He is using the ProAir Proventil inhaler. Caller later clarifies that the patient does not have asthma, he has reactive airway disease. Inquired for the ProAir Proventil Inhaler start date and dosage and caller did not provide these when requested. During the vaccine supplemental form caller provided that the patients mother reported that his arm was sore from the COVID vaccine. On 06-Nov-2019, the patient received a dose of suspect INFLUENZA VACCINE produced by unknown manufacturer (lot UT7336NA and expiration date not provided) via unknown route in the left deltoid and On 05-Nov-2021, he also received a dose of the same vaccine with same lot via unknown route in the left deltoid for prophylactic vaccination. On 26-Nov-2021, the patient received a first dose of suspect COVID-19 VACCINE MRNA not produced by Sanofi Pasteur (lot FK5127 and expiration date 31-Jan-2022) via unknown route in unknown administration site for prophylactic vaccination. On 26-Nov-2021, the patient developed a serious hives, urticaria on his arms (urticaria), hives turned and got much worse on his face, trunk, arms and legs (condition aggravated) and seasonal allergic rhinitis due to pollen and drug allergies (seasonal allergy), 2 years 20 from the first dose and 21 days from the last dose following the administration of INFLUENZA VACCINE and on the same day following the administration of COVID-19 VACCINE MRNA. This events were assessed as medically significant. It was unknown if the patient experienced any additional symptoms/events. It was reported that, at the time of administration (Covid 19 vaccine) the liquid leaked outside of the syringe and onto his arm and then onto the floor. They are not sure if the patient received the full dose of the vaccine or not. The transfer agent has already gave the information that the caller needed in regard to revaccination. No laboratory data reported. The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for Hives. turned and got much worse on his face, trunk, arms and legs then the mother gave him antihistamines and took him to the emergency room at that time. It all improved with antihistamines and there were no systemic issues present. 11. He has multiple aero. At time of reporting, the outcome was not resolved for the event urticaria, resolving for the event condition aggravated and unknown for the event seasonal allergy.; Sender's Comments: This case concerns a 07-year-old male patient who had urticaria, condition aggravated and seasonal allergy after vaccination with INFLUENZA VACCINE and COVID-19 VACCINE MRNA. Concomitant medications included SALBUTAMOL (PROVENTIL [SALBUTAMOL]). At the time of the event, the patient had ongoing Reactive airways disease on 06-NOV-2019 and Drug allergy with amoxicillin and cefdinir. the amoxicillin says serum sickness and the reaction is hives and the reaction to cefdinir is a rash. The time to onset is compatible. However, relevant laboratory data were not reported. Based upon the reported information, the role of an individual vaccine cannot be assessed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Drug allergy (amoxicillin and cefdinir. the amoxicillin says serum sickness and the reaction is hives and the reaction to cefdinir is a rash.); Reactive airways disease
Vorgeschichte
Comments: History/ Investigations: The patient is using inhalers and it is originally reported that he has asthma because she sees that there is an asthma action plan in his chart. He is using the ProAir Proventil inhaler. Caller later clarifies that the patient does not have asthma, he has reactive airway disease. Inquired for the ProAir Proventil Inhaler start date and dosage and caller did not provide these when requested. During the vaccine supplemental form caller provided that the patients mother reported that his arm was sore from the COVID vaccine.
Andere Medikamente
PROVENTIL [SALBUTAMOL]
Allergien
-
Vorherige Impfungen
-

VAERS 1764975

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

moderat
Staat
MN
Alter
31,0
Geschlecht
F
Eingang
06.10.2021
Impfdatum
05.10.2021
Beginn
05.10.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Hypoaesthesia Injection site pain Muscle tightness Muscular weakness Paraesthesia

Symptomtext

Felt pain as flu vaccine was being injected into my left deltoid (around 10:45). It was injected 1-1.5 fingers below my acromion process, seems higher than where it should've been administered. During and right after injection felt some tingling/numbness through my arm and hand. Throughout rest of day continued to feel dull pain and some pain/feeling of tightness through my left shoulder into my neck. Today (10/6) am still feeling some weakness in my left arm.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
None at this point.
Aktuelle Erkrankungen
No illnesses
Vorgeschichte
Crohn's disease, history of Leukemia at age 7
Andere Medikamente
Stelara injections every 8 weeks, Mirena IUD implanted
Allergien
Vancomycin
Vorherige Impfungen
-

VAERS 1820966

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

mild
Staat
NY
Alter
43,0
Geschlecht
F
Eingang
19.11.2021
Impfdatum
27.09.2021
Beginn
27.09.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site pain Product administered at inappropriate site Pain in extremity

Symptomtext

Injection site was in the wrong spot (too high, I am guessing because I am not a medical professional). My shoulder muscles have not been right since the injection (a lot of pain, especially after exercise/work). While lesser in intensity two months out, it still hurts, and was completely normal before the shot was given.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
A visit to the doctor for an exam at one month out was done because I did not realize that this was not "normal".
Aktuelle Erkrankungen
Migraine
Vorgeschichte
Migraine
Andere Medikamente
Topiramate 75 ml, flax seed oil, vitamin e, biotin, magnesium
Allergien
Tetracycline
Vorherige Impfungen
-

VAERS 1869625

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

mild
Staat
MN
Alter
9,0
Geschlecht
F
Eingang
15.11.2021
Impfdatum
15.11.2021
Beginn
15.11.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Rash Rash macular Somnolence

Symptomtext

About 10 minutes after both vaccines were administered, patient developed rash on both arms in elbow area, a small rash on chest, and several small blotches on neck. A single dose of oral diphenhydramine 25mg was administered. After 45 minutes of observation, the patient was released from care. Rashes were almost completely resolved, and patient said she was only experiencing mild dizziness/drowsiness.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
Vitals taken by clinic staff.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1797783

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

mild
Staat
MI
Alter
8,0
Geschlecht
M
Eingang
19.10.2021
Impfdatum
15.10.2021
Beginn
16.10.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fear Feeling abnormal Pyrexia Visual impairment

Symptomtext

Patient experienced fever night of vaccine, highest 101.0 At 0500 on 10/16 patient woke parent up stating "this night seemed so long". At 1500 on 10/16 patient was doing math homework on paper and stated numbers looked like they were getting bigger and smaller. Symptoms continued, patient stated items in surrounding area seemed to be "getting larger and smaller. Patient also stated he felt he was getting bigger and smaller. Symptoms lasted approximately 50 minutes. Patient was in distress (fearful) during symptoms, stated he was afraid it might happen again after symptoms resolved.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
None at this time.
Aktuelle Erkrankungen
None
Vorgeschichte
Seasonal allergies, eczema
Andere Medikamente
Claritin and Flonase
Allergien
None
Vorherige Impfungen
-

VAERS 1795756

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

mild
Staat
PA
Alter
5,0
Geschlecht
M
Eingang
18.10.2021
Impfdatum
16.10.2021
Beginn
17.10.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Blister Pruritus

Symptomtext

Upper arm began to blister everywhere, large blisters the size of quarters, clear fluid and itchy, took up a large surface of the upper arm

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
FPIES, eczema
Andere Medikamente
-
Allergien
Peanut, oat
Vorherige Impfungen
Not 100% sure, but mom states patient had minor skin reactions to previous flu shots (never to this extent), not sure which ones

VAERS 1779381

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

mild
Staat
MN
Alter
4,0
Geschlecht
M
Eingang
12.10.2021
Impfdatum
07.10.2021
Beginn
08.10.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site erythema Injection site reaction Injection site warmth

Symptomtext

Severe skin reaction near injection - red area and warmth that persisted for 2 days. Appeared within 24 hours of injection. Photos can be provided if needed

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1740926

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

mild
Staat
MI
Alter
65,0
Geschlecht
F
Eingang
28.09.2021
Impfdatum
21.09.2021
Beginn
23.09.2021
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Asthenia Dizziness Fall Feeling abnormal Hyperhidrosis Injection site erythema Injection site urticaria Peripheral swelling Visual impairment

Symptomtext

Patient states on 9/23/2021 patient felt weak, dizzy saw stars and slumped to the floor, did not pass out, severe sweating, L arm swollen, red with a hive like reaction around the injection site. Very weak, went to bed did not start to feel better until 9/26/2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Crohn's disease, hypothyroidism, kidney disease, and migraine
Andere Medikamente
B Complex Calcium 500 + D cetirizine estradiol Fish Oil fluticasone propionate levothyroxine Lexapro melatonin
Allergien
Keflex
Vorherige Impfungen
-

VAERS 1954425

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

gering
Staat
-
Alter
-
Geschlecht
M
Eingang
16.12.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hypersensitivity

Symptomtext

allergy reaction; Initial information was regarding an unsolicited valid non serious case was received from a consumer/non-health care professional via Medical Information (Reference number- 00886495) and transmitted to Sanofi on 06-Dec-2021. This case involves a one-years-old male patient who experienced allergy reaction (hypersensitivity), after receiving INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT]. The patient's medical history, past medical treatment(s), vaccination(s), concomitant medications and family history were not provided. On an unknown date, the patient received a 0.5 mL dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (lot UT7336NA, expiry date unknown) via an unknown route at an unknown administration site for prophylactic vaccination. On an unknown date, the patient developed non-serious allergy reaction (hypersensitivity) (unknown latency) following the administration of INFLUENZA QUADRIVAL A-B VACCINE. Details of laboratory data not reported. It was not reported if the patient received any corrective treatment for the event. At time of reporting, the outcome was unknown for the event.

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

VAERS 1931718

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

gering
Staat
VA
Alter
23,0
Geschlecht
F
Eingang
08.12.2021
Impfdatum
01.12.2021
Beginn
01.12.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Exposure during pregnancy

Symptomtext

pregnancy after receiving FLUZONE QIV PFS with no reported adverse event; Initial information regarding an unsolicited valid non-serious case was received from a physician via Agency (Reference number- 00880415) and transmitted to Sanofi on 01-Dec-2021. This case involves a 23-year-old female pregnant patient after receiving INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] (exposure during pregnancy). Data regarding this pregnancy were received prospectively. Patient was exposed to the vaccine at unknown gestation period. The date of last menstrual period was not reported. The estimated due date was not reported. The patient medical history, past medical treatment, family history and concomitant medication were not provided. On 01-Dec-2021, the patient received a 0.5 mL total dose of suspect INFLUENZA QUADRIVAL A-B VACCINE [frequency: once, strength: standard, lot UT7336NA, expiry date: 30-Jun-2022] via intramuscular route in the left deltoid for prophylactic vaccination. It was the case of vaccine exposure during pregnancy (latency same day). The patient was pregnant after received FLUZONE QUADRIVALENT vaccine. Additionally, at time of reporting, the outcome of the pregnancy is unknown.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Exposure during pregnancy
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1924845

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

gering
Staat
PA
Alter
40,0
Geschlecht
M
Eingang
06.12.2021
Impfdatum
29.11.2021
Beginn
30.11.2021
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Axillary mass Discomfort

Symptomtext

On the morning of 11/30/21, patient noticed a mass on his left axillae. On 12/1/21, the mass was large enough to cause discomfort and presented to medical clinic. Patient denies fever + chills, rashes, pain or drain on the deltoid area where the flut shot was given. On evaluation, no signs of cellulitis or concern for MRSA infection Treatment included warm compresses and NSAID treatment (ibuprofen 600 mg PO Q6H PRN). Chest CT is ordered to rule out other lymphadenopathies. Patient is to return in 1 week on 12/8/21 for follow-up.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Axillary mass
Hospital-Tage
-
Labordaten
Chest CT - scheduled for 12/8/21
Aktuelle Erkrankungen
none
Vorgeschichte
HIV, hyperlipidemia, tobacco use
Andere Medikamente
vitamin D3 2000 units, Dovato (dolutegravir/lamivudine) 50/300 mg, rosuvastatin 5 mg
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1709022

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7336NA

gering
Staat
MN
Alter
7,0
Geschlecht
F
Eingang
17.09.2021
Impfdatum
17.09.2021
Beginn
17.09.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Syringe issue

Symptomtext

AFTER INJECTING IN PATIENTS RIGHT DELTOID AREA TH FIRST INFLUENZA INJECTION -(NEEDLE FROM LOT#4155460) MALFUNCTIONED & ALL INFLUENZA LIQUID SPIRTED OUT AT THE NEEDLE/SYRINGE HUB. SO PATIENT WAS INJECTED A 2ND TIME WHICH WAS UNEVENTFUL & THE FULL DOSE WAS GIVEN. NO PROBLEMS WITH SKIN INTREGRITY NOTED A BOTH INJECTION SITES.

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