Administered fluarix. A couple hours later, patient came back stating wanted COVID vaccine

Posterior Vitrious Detachment (PVD)

patient had the vaccine on 01-07-25, noticed the reaction started on 01-09-25. patient experienced swollen arm, stinging, felt hot, sensitive to the touch, lethargic, injection site had red ring , about 5 days later, noticed bruising (size of large chicken egg) , patient iced the injection site, felt a little better , 20 days later, site still has signs of bruise mark, with redness, but not much swelling, no more lethargy, still sensitive to touch

1/27/25 Employee contacted Employee Health to report she has had a constant dull Lt upper arm and arm pit pain since her flu shot which was given on 12/23/24. She reports it becomes more intense when she lifts her arm. The employee was referred to be evaluated.

She has been crying non stop for over 3 hours, is developing a rash on her left thigh by the injection site, has not been taking her bottle, she has a fever of 101

Patient received a thjrd dose of Shingrix that was not necessary. No adverse reactions noted

Patient received 2 doses instead of 1, we did not know she had already received the vaccine. First one given on 02/22/24 and second one given 01/23/25. Patient has had no complaints other than a sore arm.

FLUZONE NP was administered to a 4-month old patient with no reported adverse event; Initial information received on 21-Jan-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves, a 4 months old and unknown gender patient was administered Influenza Usp Trival A-B Subvirion No Preservative Vaccine [Fluzone] with no reported adverse event. The patient’s past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received a dose of suspect patient was administered Influenza Usp Trival A-B Subvirion No Preservative Vaccine Suspension for injection (unknown strength, dosage, expiry date, batch number and route) via unknown administration site for Influenza with no reported adverse event (off label use) (latency- same day). Information on the batch number was requested corresponding to the one at time of event occurrence. Reportedly, Caller stated the patient was accidentally given a flu shot and wasn’t supposed to receive it until 6 months old.

Angioedema; anaphylaxis; bumped her arm; Initial information received on 20-Jan-2025 regarding an unsolicited valid serious case received from a consumer/non-health care professional. This case involves a 70 years old female patient who had angioedema, anaphylaxis and bumped her arm after receiving Influenza Quadrival A-B High Dose Hv Vaccine [Fluzone High-Dose Quadrivalent]. The patient’s past medical history, medical treatment(s), vaccination(s), concomitant medications and family history were not provided. Ona n unknown date in November 2024, the patient received a unknown dose of suspect Influenza Quadrival A-B High Dose Hv Vaccine lot U8161CA via intramuscular route in the left arm for Immunization (strength, formulation, expiry date was unknown). On an unknown date the patient developed angioedema, anaphylaxis (anaphylactic reaction) and bumped her arm (peripheral swelling) (unknown latency) following the administration of Influenza Quadrival A-B High Dose Hv Vaccine. Reportedly “She is not sure if she got the flu vaccine at that location in the past. .” Action taken was not applicable for all the events. It was not reported if the patient received a corrective treatment for the events (Angioedema, bumped her arm, anaphylaxis). At time of reporting, the outcome was Unknown for the events. Seriousness Criteria : Medically significant for the events angioedema and anaphylactic reaction.; Sender’s Comments: Sanofi Company Comment dated 23-Jan-2025 : This case involves a 70-year-old female patient who had angioedema, anaphylaxis after receiving Influenza Quadrival A-B High Dose Hv Vaccine [Fluzone High-Dose Quadrivalent].Further information regarding Past medical history, concurrent condition, concomitant medication and tolerance, 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.

I will need to get assisted suicide.; clogged arteries in my penis; heart issues; This is a spontaneous report received from a Consumer or other non HCP, Program ID. A patient (age and gender not provided) received BNT162b2 (BNT162B2 OMI XBB.1.5), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient’s relevant medical history and concomitant medications were not reported. The following information was reported: SUICIDE THREAT (medically significant), outcome “unknown”, described as “I will need to get assisted suicide.”; ARTERIAL OCCLUSIVE DISEASE (non-serious), outcome “unknown”, described as “clogged arteries in my penis”; CARDIAC DISORDER (non-serious), outcome “unknown”, described as “heart issues”. Clinical course: The patient reported that :You guys caused clogged arteries in my penis. He has been to every single hospital and been to research hospitals and now has heart issues and clogged veins in his penis from the Vaccine. The patient also stated” At just 19 years old you ruined my life. I am 22 now. I will need to get assisted suicide” The information on the batch/lot number for BNT162b2 will be requested and submitted if and when received.