Proquad is not supposed to be given to anyone over the age of 12 years old. This patient is 19 years old.
Year: 2025
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Vaccine Injury – Vaers ID:2823841 Date:01/30/2025 Age:29 Sex:M
Proquad is not supposed to be given to anyone over the age of 12 years old. This patient is 29 years old.
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Vaccine Injury – Vaers ID:2823820 Date:01/30/2025 Age:0.42 Sex:F
Patient was given extra HEP B Vaccine along with combination vaccination. NO adverse side effects or s/s of complications were observed in patient by staff.
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Vaccine Injury – Vaers ID:2823819 Date:01/30/2025 Age:53 Sex:F
A few days after patient received flublok, patient experienced a cold sensation in fingers/face which still lingers somewhat to this day. Patient has seen a few doctors in regards to this but the cause is uncertain and some believe it may possibly have been due to the vaccine.
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Vaccine Injury – Vaers ID:2823817 Date:01/30/2025 Age:56 Sex:F
Patient experienced extreme soreness on right arm and could not move it beyond an acute angle. 4 days later, on Thursday, patient found red splotches further down the upper arm with distinct borders that was tender and painful to touch. Patient can now move arm freely and still experiences mild soreness.
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Vaccine Injury – Vaers ID:2823816 Date:01/30/2025 Age:11 Sex:M
Right arm swelling (10 mm), hot to the touch, redness, and pain. Started 1 day after injections. Parents have been giving Benadryl every 4-6 hours and Tylenol for pain.
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Vaccine Injury – Vaers ID:2823815 Date:01/30/2025 Age: Sex:M
tingling in the fingers; loss of smell and taste; loss of smell and taste; This is a spontaneous report received from a Consumer or other non HCP. A 35-year-old male patient received BNT162b2 (BNT162B2 NOS), as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient’s relevant medical history was not reported. There were no concomitant medications. The following information was reported: ANOSMIA (non-serious), AGEUSIA (non-serious) all with onset 01May2024, outcome “not recovered” and all described as “loss of smell and taste”; PARAESTHESIA (non-serious) with onset 01May2024, outcome “not recovered”, described as “tingling in the fingers”. Therapeutic measures were not taken as a result of paraesthesia, anosmia, ageusia. The information on the batch/lot number for BNT162b2 will be requested and submitted if and when received.
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Vaccine Injury – Vaers ID:2823814 Date:01/30/2025 Age: Sex:M
constant pain in right side, where he got the shot and, back from lower area he got shot, towards the back and, all the way up, pain in that lower back area, the right side, basically, his lower area; shortness of breath; heart just started racing; constant pain in right side, where he got the shot; constant pain in right side; towards the lungs, right where he got the shot, right near the buttocks; This is a spontaneous report received from a Consumer or other non HCP. A 42-year-old male patient received BNT162b2 (BNT162B2), as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient’s relevant medical history included: “Diabetes” (ongoing), notes: controlled. There were no concomitant medications. Vaccination history included: Pfizer/biontech covid-19 vaccine (dose 1), for COVID-19 immunisation/COVID-19 immunisation/to leave the country. The following information was reported: BACK PAIN (non-serious), outcome “not recovered”, described as “constant pain in right side, where he got the shot and, back from lower area he got shot, towards the back and, all the way up, pain in that lower back area, the right side, basically, his lower area”; DYSPNOEA (non-serious), outcome “not recovered”, described as “shortness of breath”; PALPITATIONS (non-serious), outcome “not recovered”, described as “heart just started racing”; VACCINATION SITE PAIN (non-serious), outcome “not recovered”, described as “constant pain in right side, where he got the shot”; PAIN (non-serious), outcome “not recovered”, described as “constant pain in right side; towards the lungs, right where he got the shot, right near the buttocks”. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of back pain, dyspnoea, palpitations, vaccination site pain, pain. Additional information: The patient did not have any history of asthma in family, he did not have history of asthma. The patient other conditions was yes. The patient called and informed that the vaccine he got, maybe a year or 2 years ago, has been having some issues after having the shot. The patient clarified, he got 2 doses, the first and second. He was supposed to go back for third, wasn’t positive that was a good idea because of what was happening. He had 2 doses, Pfizer Corona vaccine, has no prior vaccinations (within 4 weeks). The patient clarifying specific issue being referred to that patient experienced after corona vaccine, stated, it has been going on for last 2 or 3 years now, basically, has shortness of breath, has constant pain down in the area. Has created issue with like, breathing, heart just started racing, have to stop or slow down little bit, trying to catch breathing. Has constant pain in right side, where he got the shot and, back from lower area he got shot, towards the back and, all the way up, pain in that lower back area, the right side, basically, his lower area, where he got the shot, towards the lungs, right where he got the shot, right near the buttocks, where he got the shot. That was where he got the shot, where he has the pain. Clarified, caller had corona vaccine shot, near buttocks, on the right side. That was where he has the pain. He clarified, the pain and shortness of breath first started at same time, almost always together. Sometimes, pain in that area, he gets a little short of breath, heart starts racing, has to stop and catch his breath. The patient still goes through both pain and shortness of breath, seemed to be progressing (worsened). The patient never experienced that before he got the shot. The patient was thinking it was ok, was probably temporary, never seemed to go away. The patient was currently in pain management, using some kind of the asthma inhalers. The patient currently, has been going to pain management facility for pain situation. He has been taking inhaler for situation sometimes. The patient kept letting them know the situation, they still were not sure what situation was, they said they did not see anything there. They kept explaining situation, has not gotten anywhere with it. The patient clarified, referring to medical help or financial compensation. The information on the batch/lot number for BNT162b2 will be requested and submitted if and when received.
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Vaccine Injury – Vaers ID:2823813 Date:01/30/2025 Age: Sex:M
Died; This is a spontaneous report received from a consumer. An adult male patient received BNT162b2 Omicron (KP.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for COVID-19 immunisation. The patient’s relevant medical history included: “Hospitalization” (ongoing). The patient took concomitant medications. The patient received other medications in two weeks. Vaccination history included: COVID-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunization; COVID-19 vaccine (DOSE NUMBER UNKNOWN (BOOSTER); MANUFACTURER UNKNOWN), for COVID-19 immunization. No other vaccine was administered in four weeks or on the same date of the suspect COVID-19 vaccine. The following information was reported: DEATH (death, prolonged hospitalization, disability, life threatening, medically significant), outcome “fatal”, described as “Died”. Therapeutic measures were taken as a result of death. The date and cause of death for the patient were unknown. It was not reported if an autopsy was performed. The patient’s child was doing this for the patient as he died from getting the COVID-19 vaccines and boosters. The adverse events resulted in death, prolongation of existing hospitalization (treatment received during existing hospitalization), life-threatening illness (immediate risk of death from the event), and disability or permanent damage. Per patient’s child, the patient did not recover from the event. The information on the batch/lot number for BNT162b2 Omicron (KP.2) will be requested and submitted if and when received.; Reported Cause(s) of Death: Died