Approximately 12 hours after administration, pt reported rigors, chills, GI discomfort. Progressed to myalgias, arthralgias, chest discomfort, cough, rash. Fever in office on 1/28/2025 of 103.1 (no fever management prior to visit.)

PATIENT STATES THAT INJECTION SITE FELT FINE FOR A FEW DAYS AFTER THE VACCINE WAS GIVEN. AS TIME WENT ON NOTICED TINGLING AT THE INJECTION SITE AND FEELING LIKE MUSCLES WERE MOVING (DESCRIBED LIKE THE MUSCLE WAS A BED OF WORMS). PATIENT FEELS LIKE THE SENSATION IS GETTING MORE INTENSE AS TIME GOES ON.

No additional AE; HCP called to report a Temperature Excursion on case number 02740636. The case is still ongoing and it could not be confirmed if the products were still supported. The HCP reports that PROQUAD was inadvertently administered after suffering from a Te; This spontaneous report has been received from a Nurse referring to a patient of an unknown age and gender. The patient’s concomitant medications included sterile diluent (MERCK STERILE DILUENT). The patient’s pertinent medical history, concurrent conditions, concomitant medications and previous drugs reactions or allergies were not reported. On 11-NOV-2024, the patient was vaccinated with an improperly stored dose of measles, mumps, rubella and varicella (oka-merck) virus vaccine live (rHA[recombinant human albumin]) (PROQUAD) injection, 0.5 milliliter, administered as prophylaxis (Lot No. Y013574 has been verified to be a valid lot number for [measles, mumps, rubella and varicella (oka-merck) virus vaccine live], expiration date was not reported but upon internal validation established as 03-FEB-2026) (dose number, route of administration, anatomical location of administration and vaccination scheme frequency were not provided) (product storage error), after a temperature excursion of -11.6 degree Celsius (C) during a time frame of 3 hours, 5 minutes and 0 seconds. Previous temperature excursions could not be confirmed. No additional adverse event (AE) was reported (no adverse event). This is one of several reports received from the same reporter.; Sender’s Comments: US-009507513-2501USA007066: US-009507513-2501USA008866: US-009507513-2501USA008885: US-009507513-2501USA009045: US-009507513-2501USA008880: US-009507513-2501USA008935: US-009507513-2501USA008877: US-009507513-2501USA008882: US-009507513-2501USA007047: US-009507513-2501USA007446: US-009507513-2501USA008861:

abdominal pain; bowel inflammation; low-grade fevers; psoriatic arthritis, joint pain,loss of range of motion/lack of control of some muscles and fingers; second dose 22-APR-2022; fibromyalgia, severe chronic pain,weakness/joint pain; POTS-like symptoms/tachycardia/postural hypotesion/elevated antinuclear antibodies/dizziness; Information has been received from a lawyer regarding a case in litigation, concerning an adult female patient (pt) of unknown age. The pt’s medical history, concurrent conditions, and concomitant medications were not provided. On 23-APR-2021 (when she was 30-years old), the pt was inoculated with the first dose of Quadrivalent Human Papillomavirus (Types 6,11,16,18) Recomb. Vaccine (GARDASIL) intramuscular injection as prevention of cervical cancer (dose, route of administration, anatomical location, lot number, and expiration date were not provided). Subsequently on 22-APR-2022, she received the second dose of the vaccine (Inappropriate schedule of product administration), both vaccines were administered under her physician’s recommendation. On approximately 30-APR-2021 (reported as “within approximately a week from receiving the first Gardasil injection”), the pt began experiencing unusual joint pain. The pain began at the knees and progressed to the pt’s shoulder joints and smaller joints. In addition, she began experiencing daily POTS-like (postural orthostatic tachycardia syndrome) symptoms, including tachycardia, dizziness, postural hypotension, and abdominal pain. Due to the abdominal pain, she made reoccurring visits to the hospital. As well as relied on medications such as hydroxychloroquine (PLAQUENIL) and various over-the-counter pain relief items like heat wraps, lidocaine patches, NSAID creams, and more. Unfortunately, none of these remedied the pain. Moreover, on an unknown date, the pt was diagnosed with elevated antinuclear antibodies, low-grade fevers, severe chronic pain, loss of range of motion, weakness, and lack of control of some muscles and fingers, and bowel inflammation. Post vaccination, the pt visited numerous specialists to evaluate her symptoms, such as an orthopedist, gastroenterologist, rheumatologist, and the emergency room. Thus, she was diagnosed with psoriatic arthritis and fibromyalgia. As the months progressed, so did the pt’s injuries. She was seen by multiple physicians and specialists for her complaints which now included: joint pain, tachycardia dizziness, POTS-like symptoms, postural hypotension, abdominal pain, low-grade fevers, chronic pain, loss of range of motion, weakness, muscle function loss, bowel inflammation, and elevated antinuclear antibodies levels. As a result of her post Quadrivalent Human Papillomavirus (Types 6,11,16,18) Recomb. Vaccine (GARDASIL) symptoms, the pt has been unable to engage in activities that a normal young person would enjoy. As the sole caregiver and a healthcare professional, her career has been significantly impacted by the physical limitations caused by these symptoms. She was no longer able to complete a full shift without experiencing considerable pain and now depended on lidocaine patches for relief. Additionally, the medications that help her manage these symptoms have severely restricted her ability to pursue her personal aspirations, such as traveling, making such goals nearly impossible to achieve. Furthermore, the medication prescribed to manage her symptoms carries the risk of causing blindness, instilling a profound fear for the long-term quality of her life and future. Based upon her chronic and severe symptoms, the pt has been diagnosed with various medical conditions, including but not limited to, psoriatic arthritis, fibromyalgia, and POTS-like symptoms. In addition, the pt contended that her Quadrivalent Human Papillomavirus (Types 6,11,16,18) Recomb. Vaccine (GARDASIL) injections caused her to develop serious and debilitating autoimmune and autonomic injuries, including but not limited to psoriatic arthritis, fibromyalgia, and POTS-like symptoms, as well as a constellation of adverse events symptoms, complications, injuries, and other adverse events, many of which were alleged herein and all of which were caused by Quadrivalent Human Papillomavirus (Types 6,11,16,18) Recomb. Vaccine (GARDASIL) or otherwise linked to her Quadrivalent Human Papillomavirus (Types 6,11,16,18) Recomb. Vaccine (GARDASIL)-induced autoimmune and autonomic disorder. Moreover, the pt sustained that The Company’s negligence was the proximate cause of the injuries, harm, and economic losses that she suffered, and will continue to suffer, as described herein. Additionally, as a direct and proximate result of her vaccine-induced injuries the pt has suffered considerable non-economic and economic losses, including considerable financial expenses for medical care and treatment, and diminished income capacity and will continue to incur. The patient had not recovered from the adverse events, and it was considered the events to be related to Quadrivalent Human Papillomavirus (Types 6,11,16,18) Recomb. Vaccine (GARDASIL). Upon internal review the event psoriatic arthropathy was considered to be medically significant. Lot numbers are being requested and will be submitted if received.

Myocarditis, typical heart attack symptoms. Hospital 3 days end result us unknow cause of myocarditis

Body hives, red splotches on arms, thighs, stomach , shoulders, back

Received TDAP vaccine IM to the left deltoid muscle. Venipuncture for labs was then performed. Lab draw was completed and he complained of feeling hot. His skin then became clammy and he appeared to black out for approx 1 second. He immediately regained consciousness. He was diaphoretic. He was placed in supine position on exam table. He remained alert. Blood pressure was 91/54. BP was 129/90 prior to TDAP dose. He then c/o feeling dizzy, lightheaded, nauseous and reported a stomach ache. He was allowed to rest and provided a gatorade to hydrate himself. After approximately 25 minutes of monitoring he reported feeling better but felt drained with residual nausea. Repeat BP 136/91.

nausea, vomiting, short bouts of dizziness Symptoms improved within 15 hours. No medication needed. Could this have just been a stomach virus? No one else around me has been sick with stomach virus.

Father came into pickup line asking clerk about vaccines for him and son. I overheard and thought I heard flu vaccines. I processed and administered. A couple hours later, father came and said wanted COVID vaccine

Sometime between June of 2021, and early 2022, Moderna vaccination resulted in permanent damage to my reproductive system. Tests done in 2022 and 2023 have shown that there are no sperm cells seen in the samples. Before vaccination, semen tests (done in 2015 and June 2021) have shown normal amount of motile sperm cells. The detailed timeline of semen tests performed is shown on the next page. There were no other events or problems (no health problems, no injuries) that would explain that sperm cells stopped generating in my reproductive system, pointing to vaccination as the reason of the problem. (See next page) Timeline of tests done for semen analysis before and after vaccination: Oct 20, 2023 – Lab test of semen – no sperm cells seen Feb 17, 2023 – test of semen – no sperm cells seen Feb 10, 2023 – test of semen – no sperm cells seen During 2022 – self-tests with microscope, seen gradual decrease of moving sperm cell numbers, and moving cells seen not on every try Dec 12, 2021 – Moderna 60H21A mRNA booster June 29, 2021 – Lab test of semen and count – normal results and good motility (12×10^6) May 16, 2021 – Moderna 014C21A mRNA vaccination Apr 18, 2021 – Moderna 046B21A mRNA vaccination Jan 2015 – Lab test of semen and count – normal results and good motility (14×10^6) Another troubling fact is that my wife, who received the same Moderna vaccinations, have lost ability to remember any new information sometime in summer of 2021, and after that her brain degeneration was developing exponentially. Please see report VAERS ID: 2822907, E-Report Number: 1050478 for wife’s case. In addition to this permanent damage to reproductive system, I have also started to notice, since August 2021, heart palpitations. I never had any problems with heart before. I have followed with cardiologist. Ultrasound tests haven’t shown any specific issues in the heart. After about two years, palpitations were gone. However, reproductive system was damaged permanently, as confirmed by periodic tests done in 2024 and 2025. Seeing that two people who received same vaccinations had damaging impacts, one can conclude that either a) it is possible that these specific batches of vaccines are in particular damaging; or b) patient and I were both damaged by vaccine because we came from a very similar ethnic group. Hope science research on these questions will be launched, helping people in the future.