| ID | Age | Sex | State | Date ▼ | Onset Days | Vaccine | Manufacturer | Lot # | Symptoms | Narrative | 💀 | 🏥 | 🚑 | ♿ | ⚠️ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2849910 | 66 | F | VA | 07/16/2025 |
COVID19-2 |
MODERNA |
055F22B |
Near death experience, Urticaria chronic
Near death experience, Urticaria chronic
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I think I am dying from this vaccine; experiencing "hives" since June 2024 / Chronic spont...
I think I am dying from this vaccine; experiencing "hives" since June 2024 / Chronic spontaneous hives; This spontaneous case was reported by a consumer and describes the occurrence of NEAR DEATH EXPERIENCE (I think I am dying from this vaccine) in a 66-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 055F22B) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Previously administered products included for Drug use for unknown indication: Tylenol (Patient took a couple of Tylenol and felt better). Past adverse reactions to the above products included No adverse effect with Tylenol. On 09-Oct-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular use) 1 dosage form. In June 2024, the patient experienced URTICARIA CHRONIC (experiencing "hives" since June 2024 / Chronic spontaneous hives). On an unknown date, the patient experienced NEAR DEATH EXPERIENCE (I think I am dying from this vaccine) (seriousness criterion medically significant). The patient was treated with Prednisone at an unspecified dose and frequency. At the time of the report, NEAR DEATH EXPERIENCE (I think I am dying from this vaccine) and URTICARIA CHRONIC (experiencing "hives" since June 2024 / Chronic spontaneous hives) outcome was unknown. No concomitant medications were reported. The reporter received her first Moderna COVID-19 vaccine in Dec-2020. After the first injection, her injection site arm was very sore. She received her second Moderna COVID-19 vaccine in Jan-2021, and she experienced a sore injection site arm, fatigue, headache, muscle pain, and joint pain. These effects lasted for 24 hours. In Nov-2021, she received her booster dose of the Moderna COVID-19 vaccine in her right arm shoulder deltoid muscle as an intramuscular injection. After the booster, she had a sore right arm, chills, a fever of 101 degrees Fahrenheit, teeth chattering from feeling extremely cold, and a swollen right arm. It was reported that the reporter had experienced hives since Jun-2024, which she associated from her Moderna Covid-19 vaccine doses. She mentioned that she received vaccine shots except in 2025 and reported that the vaccination information she had was old. However, she was not able to provide the complete information regarding her doses. She reported that she reached out to multiple specialists, including an oncologist, rheumatologist, and allergist. She also mentioned that antihistamines and prednisone did not help her to treat the hives. She reported that she was not properly informed of the side-effects she may experience after receiving the vaccine. She was experienced awful symptoms and stated that she thought that it was killing her and she thought she was dying from that vaccine. She also added that her dermatologist, allergist, rheumatologist, and family doctor said that she had Chronic spontaneous hives. It was unknown if the patient experienced any additional symptoms or events. This case was linked to MOD-2022-516527 (Patient Link).; Reporter's Comments: The benefit-risk relationship of product is not affected by this report.
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| 2849911 | 0.5 | M | MA | 07/16/2025 |
COVID19 RVX RVX TDAP |
MODERNA UNKNOWN MANUFACTURER UNKNOWN MANUFACTURER UNKNOWN MANUFACTURER |
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Irritability, Pyrexia, Somnolence; Irritability, Pyrexia, Somnolence; Irritabili...
Irritability, Pyrexia, Somnolence; Irritability, Pyrexia, Somnolence; Irritability, Pyrexia, Somnolence; Irritability, Pyrexia, Somnolence
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sleepy; irritable; fever; This spontaneous case was reported by a non-health professional and descri...
sleepy; irritable; fever; This spontaneous case was reported by a non-health professional and describes the occurrence of SOMNOLENCE (sleepy), IRRITABILITY (irritable) and PYREXIA (fever) in a 6-month-old male patient who received mRNA-1273.712 (MODERNA COVID-19 VACCINE 2024-2025 PFS) for COVID-19 prophylaxis. Co-suspect products included non-company products RSV vaccine for an unknown indication, Diphtheria vaccine toxoid, Pertussis vaccine acellular, Tetanus vaccine toxoid (Tdap) for an unknown indication and Rotavirus vaccine for an unknown indication. No Medical History information was reported. On 11-Jul-2025, the patient received first dose of mRNA-1273.712 (MODERNA COVID-19 VACCINE 2024-2025 PFS) (Intramuscular use) 1 dosage form, dose of RSV vaccine (unknown route) 1 dosage form, dose of Diphtheria vaccine toxoid, Pertussis vaccine acellular, Tetanus vaccine toxoid (Tdap) (unknown route) 1 dosage form and dose of Rotavirus vaccine (unknown route) 1 dosage form. On 11-Jul-2025, the patient experienced SOMNOLENCE (sleepy), IRRITABILITY (irritable) and PYREXIA (fever). The patient was treated with Paracetamol (Tylenol infant) in July 2025 at a dose of 2 milliliter every four hours. On 12-Jul-2025, SOMNOLENCE (sleepy), IRRITABILITY (irritable) and PYREXIA (fever) had resolved. For mRNA-1273.712 (MODERNA COVID-19 VACCINE 2024-2025 PFS) (Intramuscular use), the reporter did not provide any causality assessments. No concomitant medications provided by the reporter. It was reported that Infant received first dose of Moderna Covid vaccine along with RSV, TDaP, rotavirus, and other standard six-month vaccines. Post vaccination patient was developed fever and patient was sleepy with irritable symptom which was started about two hours after vaccination; side effects were lasted approximately 36 hours. The patient did not experience any additional symptoms or events.
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| 2849912 | 12 | F | TX | 07/16/2025 |
COVID19 COVID19 |
PFIZER\BIONTECH PFIZER\BIONTECH |
EW0175 EW0175 |
Aphonia, Blood test, Chills, Erythema, Myasthenia gravis; Nasopharyngitis, Produ...
Aphonia, Blood test, Chills, Erythema, Myasthenia gravis; Nasopharyngitis, Productive cough, Pyrexia, Tremor
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Myasthenia gravis; High fever; Got very sick; Chilled and cold; Got very sick; Chilled and cold; Sta...
Myasthenia gravis; High fever; Got very sick; Chilled and cold; Got very sick; Chilled and cold; Started showing tremor signs/Body shakes; Started turning red; Lost her voice; Phlegm in her throat/Snot in her throat really bad; This is a spontaneous report received from a Consumer or other non HCP. A 16-year-old female patient received BNT162b2 (BNT162B2), on 02Sep2021 as dose 2, single (Lot number: EW0175) at the age of 12 years intramuscular, in arm for covid-19 immunisation. The patient's relevant medical history included: "mild asthma" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1, Single), administration date: 12Aug2021, when the patient was 12-year-old, for Covid-19 immunization. The following information was reported: MYASTHENIA GRAVIS (hospitalization, medically significant), outcome "not recovered"; PYREXIA (non-serious), outcome "unknown", described as "High fever"; CHILLS (non-serious), NASOPHARYNGITIS (non-serious), outcome "unknown" and all described as "Got very sick; Chilled and cold"; TREMOR (non-serious), outcome "unknown", described as "Started showing tremor signs/Body shakes"; ERYTHEMA (non-serious), outcome "unknown", described as "Started turning red"; APHONIA (non-serious), outcome "unknown", described as "Lost her voice"; PRODUCTIVE COUGH (non-serious), outcome "unknown", described as "Phlegm in her throat/Snot in her throat really bad". The events "myasthenia gravis", "high fever", "got very sick; chilled and cold", "started showing tremor signs/body shakes", "started turning red", "lost her voice" and "phlegm in her throat/snot in her throat really bad" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood test: Unknown results. Therapeutic measures were taken as a result of myasthenia gravis, productive cough. Clinical course: The reporter's daughter received the Pfizer Covid-19 vaccine in 2021 and 3 to 6 months after she receive that shot, she started having side effects of different things and then six months she was diagnosed with a rare disease. The patient was very healthy before she receives the covid shot and after that, she started showing side effects of things. The disease was not in their family, nobody ever has it, and they believe it's from the covid shot because she started showing side effects because the covid shot made her sick and she took Pfizer. The patient had high fever, and she got very sick and chilled and cold and about two months she had the shot, she started showing tremor signs and they had to take her to a tremor doctor, a neurologist. She started showing tremors, then after tremor she started having body shakes, after the body shake, she started having double vision. She started having snot in her throat really bad. They thought it was a sinus problem. After that she started turning red. Basically, after that she started choking on food, could not swallow, lost her voice and basically when they took her to the doctor, they are saying that she has a rare disease called Myasthenia Gravis (MG). The patient has been seeing a doctor since 2021 with different side effects. The reporter has been telling him it was covid (vaccine) and the doctor did not say anything because they don't want sued and she was in the hospital in February, Feb2025 when they told us that all the symptoms she is been having since the covid vaccine is called Myasthenia Gravis. She has to take medicine for the rest of her life, she has had blood work done (results unknown). Myasthenia Gravis was diagnosed this February saying that all the symptoms of everything that she has had from choking to, with all the phlegm in her throat is Myasthenia Gravis. She is got a disease that she will never get over. It's an immune disease that she will have to take the medicine for the rest of her life. The doctor did not know what was wrong with her until now. The spit on her throat caused from this shot, they thought it was a sinus problem. They did not know why she had double vision. They did not know why she was turning red and running fever. They did not know why she was choking on food and basically, they ran a test where they take wires and stick it in the nerves, and it came back that she has this disease. So, they have been treating her for, like that she has just a sinus infection and it was not that. It's signs of a disease and you have to get a rare doctor, that's a neurologist, finally diagnosed her with this after a test in a (Name withheld). Her regular doctor, none of these people knew what was happening to her. They did not know why. They just did not know it was a side effect of covid shot or if it was sinuses, if it was the flu and then now, they said that she has got a disease, and she started having these problems two to three months after the covid shot and it keeps getting worse and worse.
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| 2849913 | 37 | F | CT | 07/16/2025 |
RAB RAB RAB RAB RAB RAB RAB RAB RAB RAB RAB RAB RAB RAB RAB RAB RAB RAB UNK UNK UNK UNK UNK UNK |
NOVARTIS VACCINES AND DIAGNOSTICS NOVARTIS VACCINES AND DIAGNOSTICS NOVARTIS VACCINES AND DIAGNOSTICS NOVARTIS VACCINES AND DIAGNOSTICS NOVARTIS VACCINES AND DIAGNOSTICS NOVARTIS VACCINES AND DIAGNOSTICS SANOFI PASTEUR SANOFI PASTEUR SANOFI PASTEUR SANOFI PASTEUR SANOFI PASTEUR SANOFI PASTEUR NOVARTIS VACCINES AND DIAGNOSTICS NOVARTIS VACCINES AND DIAGNOSTICS NOVARTIS VACCINES AND DIAGNOSTICS NOVARTIS VACCINES AND DIAGNOSTICS NOVARTIS VACCINES AND DIAGNOSTICS NOVARTIS VACCINES AND DIAGNOSTICS UNKNOWN MANUFACTURER UNKNOWN MANUFACTURER UNKNOWN MANUFACTURER UNKNOWN MANUFACTURER UNKNOWN MANUFACTURER UNKNOWN MANUFACTURER |
Unknown Unknown Unknown Unknown Unknown Unknown Unknown Unknown Unknown Unknown Unknown Unknown |
Anxiety, Chest pain, Condition aggravated, Feeding disorder, Hallucination; Inap...
Anxiety, Chest pain, Condition aggravated, Feeding disorder, Hallucination; Inappropriate schedule of product administration, Insomnia, Malaise, Myoclonus, Tinnitus; Tremor, Weight decreased; Anxiety, Chest pain, Condition aggravated, Feeding disorder, Hallucination; Insomnia, Interchange of vaccine products, Malaise, Myoclonus, Palpitations; Tinnitus, Tremor, Weight decreased; Anxiety, Chest pain, Condition aggravated, Feeding disorder, Hallucination; Inappropriate schedule of product administration, Insomnia, Malaise, Myoclonus, Tinnitus; Tremor, Weight decreased; Anxiety, Chest pain, Condition aggravated, Feeding disorder, Hallucination; Insomnia, Interchange of vaccine products, Malaise, Myoclonus, Palpitations; Tinnitus, Tremor, Weight decreased; Anxiety, Chest pain, Condition aggravated, Feeding disorder, Hallucination; Inappropriate schedule of product administration, Insomnia, Malaise, Myoclonus, Tinnitus; Tremor, Weight decreased; Anxiety, Chest pain, Condition aggravated, Feeding disorder, Hallucination; Insomnia, Interchange of vaccine products, Malaise, Myoclonus, Palpitations; Tinnitus, Tremor, Weight decreased; Anxiety, Chest pain, Condition aggravated, Feeding disorder, Hallucination; Inappropriate schedule of product administration, Insomnia, Malaise, Myoclonus, Tinnitus; Tremor, Weight decreased; Anxiety, Chest pain, Condition aggravated, Feeding disorder, Hallucination; Insomnia, Interchange of vaccine products, Malaise, Myoclonus, Palpitations; Tinnitus, Tremor, Weight decreased
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1st dose on day 0 and the 2nd dose on day 7 since they missed day 3. since getting the 2nd dose; exp...
1st dose on day 0 and the 2nd dose on day 7 since they missed day 3. since getting the 2nd dose; experienced hallucinations; very sick; chest pains, firework feeling in their chest- like a heart attack; chest pains, firework feeling in their chest- like a heart attack; jump at sleep /could not sleep/insomnia; lost 20 pounds; tremors in hands; anxiety; really bad ringing in my ears that persisted has been since the injection/tinnitus; could not eat; Initial information received on 08-Jul-2025 regarding an unsolicited valid serious case received from a consumer/non-hcp (health care professional). This case involves a 37 years old female patient who received 1st dose of Rabies vaccine inact (chick embryo) (Rabavert) on day 0 and 2nd dose of rabies (HDC) vaccine [Imovax rabies] on day 7 since they missed day 3 and had very sick, hallucinations, chest pains, firework feeling in their chest- like a heart attack, chest pains, jump at sleep/could not sleep/insomnia, lost 20 pounds, tremors in hands, anxiety, really bad ringing in my ears that persisted has been since the injection/tinnitus and could not eat. The patient's past medical history included Illness anxiety disorder. The patient's past medical treatment(s), vaccination(s) and family history were not provided. On an unknown date in March 2025, the patient received an unknown dose (dose 1) of suspect Rabies vaccine inact (chick embryo) on day 0 (unknown formulation) not produced by Sanofi Pasteur for prophylactic vaccination (Immunisation) and received an unknown dose (dose 2) of suspect rabies (HDC) vaccine (formulation: Powder and solvent for suspension for injection) for rabies (Rabies immunization) on day 7 both (lot number, strength and expiry date not reported) via unknown route in unknown administration site since they missed day 3 (routine immunisation schedule not administered) (unknown latency). On an unknown date in 2025, the patient developed very sick (illness), hallucination, chest pains, firework feeling in their chest like a heart attack (chest pain) (palpitations), jump at sleep /could not sleep/insomnia (insomnia), lost 20 pounds (weight decreased), tremors in hands (tremor), anxiety, really bad ringing in my ears that persisted has been since the injection/tinnitus (tinnitus), could not eat (Feeding disorder) (unknown latency). Relevant laboratory test results included: Weight decreased - On an unknown date in 2025: [lost 20 pounds]. Reportedly, They had a bat in their kitchen and their doctor recommended that they get vaccination just in case. Patient stated that they got their vaccination around 11-Mar-2025. Since getting the 2nd dose, which they think was IMOVAX, they have been very sick and have been in and out of hospital. They said that it was hard to say if some of the side effects that they were experiencing could be due to the other medications they were put on due to the side effects they were experiencing. But the really bad ringing in my ears that persisted has been since the injection. The first 2 months were bad, they could not eat or sleep and experiencing tremors. They mention that they have never been vaccinated before and they have always been kind of hypochondriac. So that may be where the anxiety is from and may be it was their body being unused with vaccination. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the events (illness, hallucination, chest pain, palpitations, insomnia, weight decreased, tremor, anxiety, tinnitus and eating disorder). At time of reporting, the outcome was Unknown for the events (illness, eating disorder, weight decreased, chest pain and palpitations) and was not recovered/ not resolved for rest other events. Seriousness criteria: The event (hallucination) was assessed as medically significant. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.; Sender's Comments: Sanofi company comment dated 15-Jul-2025: This case involves a 37 years old female patient who received 1st dose of Rabies vaccine inact (chick embryo) (Rabavert) on day 0 and 2nd dose of rabies (HDC) vaccine [Imovax rabies] on day 7 since they missed day 3 and had very sick, hallucinations, chest pains, firework feeling in their chest- like a heart attack, chest pains, jump at sleep/could not sleep/insomnia, lost 20 pounds, tremors in hands, anxiety, really bad ringing in my ears that persisted has been since the injection/tinnitus and could not eat. The time to onset was compatible with the role of vaccine. The clinical course of the event was not provided. Patient's past medical history of anxiety disorder cannot be ignored either. Furthermore, information regarding condition at the time of vaccination, lab data excluding other predisposing etiologies would be needed for complete assessment of the case. Based upon the reported information, the role of the suspect vaccine cannot be assessed
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| 2849914 | 12 | M | AR | 07/16/2025 |
MNQ |
SANOFI PASTEUR |
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Inappropriate schedule of product administration
Inappropriate schedule of product administration
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Child received two doses of MENACTRA in 2018 (two months apart: 9/4/2018 and 11/20/2018) and now the...
Child received two doses of MENACTRA in 2018 (two months apart: 9/4/2018 and 11/20/2018) and now the patient is due for a dose at 18, with no reported adverse event; Initial information received on 09-Jul-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 12 years old male patient who received two doses of Meningococcal A-C-Y-W135 (D Conj) Vaccine [Menactra] in 2018 (two months apart: 04-Sep-2018 and 20-Nov-2018) and now the patient is due for a dose at 18, with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 04-Sep-2018, the patient received a dose 1 of suspect Meningococcal A-C-Y-W135 (D Conj) Vaccine, Solution for injection, (lot number, expiry date and strength not reported) via unknown route in unknown administration site for Immunization. On 20-Nov-2018, (two months apart) the patient received another dose 2 of the same suspect vaccine for Immunization and now the patient is due for a dose at 18, with no reported adverse event (inappropriate schedule of product administration) (latency: same day). Information on the batch number was requested corresponding to the one at time of event occurrence. Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
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| 2849915 | 79 | F | OK | 07/16/2025 |
TDAP VARZOS |
GLAXOSMITHKLINE BIOLOGICALS GLAXOSMITHKLINE BIOLOGICALS |
75G27 |
Blister, Herpes zoster, Neck pain, Pain, Paraesthesia; Blister, Herpes zoster, N...
Blister, Herpes zoster, Neck pain, Pain, Paraesthesia; Blister, Herpes zoster, Neck pain, Pain, Paraesthesia
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Two (2) days after receiving the first Shingrix vaccine shot I began having a sore/tender area at ba...
Two (2) days after receiving the first Shingrix vaccine shot I began having a sore/tender area at base of my neck. By Saturday 4 days post injection blisters formed in that area which was the size of a silver dollar. I also had stinging/tingling across my shoulder and into my neck. Next day I was seen at urgent care and diagnosed with shingles and prescribed an antiviral med and topical lidocaine. HX: I received the original shingles vaccine around 2005 and 2 years later broke out in a more severe case of shingles compared to this episode.
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| 2849916 | 88 | M | MN | 07/16/2025 |
COVID19 |
MODERNA |
026A21A |
COVID-19, Death, SARS-CoV-2 RNA increased
COVID-19, Death, SARS-CoV-2 RNA increased
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HOSPITALIZATION AND DEATH RELATED TO COVID-19 FOLLOWING COMPLETION OF PRIMARY COVID VACCINE SERIES
HOSPITALIZATION AND DEATH RELATED TO COVID-19 FOLLOWING COMPLETION OF PRIMARY COVID VACCINE SERIES
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| 2849917 | 60 | F | FL | 07/16/2025 |
PNC20 PNC20 |
PFIZER\WYETH PFIZER\WYETH |
ln4927 ln4927 |
Induration, Pain, Rash, Rash erythematous, Skin warm; Swelling
Induration, Pain, Rash, Rash erythematous, Skin warm; Swelling
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The day after patient experienced swelling, and the development of a streaky rash. The day after pai...
The day after patient experienced swelling, and the development of a streaky rash. The day after pain got worse and is now decribe as shooting pain rash is red, hot, and fells hard to the touch per pt.
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| 2849918 | 66 | M | MA | 07/16/2025 |
TDAP |
GLAXOSMITHKLINE BIOLOGICALS |
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Back pain, Hyperhidrosis, Hypoaesthesia, Pain, Pain in extremity
Back pain, Hyperhidrosis, Hypoaesthesia, Pain, Pain in extremity
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14 hours after vaccination, at 1:00am, I awaoke sweating heavily, with pain in my upper back near my...
14 hours after vaccination, at 1:00am, I awaoke sweating heavily, with pain in my upper back near my right shoulder blade, with pain shooting through my right arm, and pain and numbness in my right hand. The Pain in my back is still persisting today. 9 days after the vaccination.
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| 2849919 | 67 | F | NC | 07/16/2025 |
PNC21 |
MERCK & CO. INC. |
Y019157 |
Injection site erythema, Peripheral swelling, Pyrexia
Injection site erythema, Peripheral swelling, Pyrexia
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Patient states she experienced a fever and developed a red and swollen arm. The patient showed me a ...
Patient states she experienced a fever and developed a red and swollen arm. The patient showed me a picture in which the redness traveled from the injection site down to her elbow. She states these symptoms lasted for ~1 week.
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| 2849920 | 74 | F | 07/16/2025 |
RSV VARZOS |
GLAXOSMITHKLINE BIOLOGICALS GLAXOSMITHKLINE BIOLOGICALS |
CE9C9 3273H |
Expired product administered, Pain in extremity; Expired product administered, P...
Expired product administered, Pain in extremity; Expired product administered, Pain in extremity
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Found out right after patient left that the antigen component of Arexvy was expired on 7/6/25 (admin...
Found out right after patient left that the antigen component of Arexvy was expired on 7/6/25 (administered on 7/15/25). Checked with patient that she is not experiencing any unusual side effects other than sore arms. Patient will return to pharmacy for revaccination as recommended by the CDC.
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| 2849921 | 1.33 | F | VA | 07/16/2025 |
UNK |
UNKNOWN MANUFACTURER |
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Febrile convulsion
Febrile convulsion
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febrile seizure
febrile seizure
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| 2849923 | 30 | F | MO | 07/16/2025 |
COVID19 COVID19 COVID19 COVID19 COVID19 COVID19 COVID19 COVID19 COVID19 COVID19 COVID19 COVID19 COVID19 COVID19 COVID19 |
PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH |
FA6780 FA6780 FA6780 FA6780 FA6780 FA7485 FA7485 FA7485 FA7485 FA7485 FP7137 FP7137 FP7137 FP7137 FP7137 |
Arthralgia, Autonomic nervous system imbalance, Blood creatine phosphokinase dec...
Arthralgia, Autonomic nervous system imbalance, Blood creatine phosphokinase decreased, Burning sensation, Cardiac disorder; Echocardiogram, Electrocardiogram QT prolonged, Electrocardiogram ambulatory, Fatigue, Haemangioma of bone; Hypoaesthesia, Impaired work ability, Magnetic resonance imaging head abnormal, Magnetic resonance imaging spinal abnormal, Muscular weakness; Neutrophil count abnormal, Paranasal cyst, Polyneuropathy, Sleep study normal, Tachycardia; Vertigo, Visual impairment, White blood cell count increased; Arthralgia, Autonomic nervous system imbalance, Blood creatine phosphokinase decreased, Burning sensation, Cardiac disorder; Echocardiogram, Electrocardiogram QT prolonged, Electrocardiogram ambulatory, Fatigue, Haemangioma of bone; Hypoaesthesia, Impaired work ability, Magnetic resonance imaging head abnormal, Magnetic resonance imaging spinal abnormal, Muscular weakness; Neutrophil count abnormal, Paranasal cyst, Polyneuropathy, Sleep study normal, Tachycardia; Vertigo, Visual impairment, White blood cell count increased; Arthralgia, Autonomic nervous system imbalance, Blood creatine phosphokinase decreased, Burning sensation, Cardiac disorder; Echocardiogram, Electrocardiogram QT prolonged, Electrocardiogram ambulatory, Fatigue, Haemangioma of bone; Hypoaesthesia, Impaired work ability, Magnetic resonance imaging head abnormal, Magnetic resonance imaging spinal abnormal, Muscular weakness; Neutrophil count abnormal, Paranasal cyst, Polyneuropathy, Sleep study normal, Tachycardia; Vertigo, Visual impairment, White blood cell count increased
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Left shoulder pain and numbness. Burning sensation down shoulder and arm. Weakness in arm. Onset wi...
Left shoulder pain and numbness. Burning sensation down shoulder and arm. Weakness in arm. Onset within 48 hours of injection but progressed until I received treatment in 2022. Poly neuropathy starting in 2022 and has continued into 2025. Chronic fatigue since 2021. Vision changes, vertigo , tachycardia and other cardiac issues starting in October 2024 and since continued. Had to resign from job as RN due to chronic and worsening symptoms. Dx autonomic dysfunction.
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| 2849924 | 1.08 | F | ID | 07/16/2025 |
HIBV |
SANOFI PASTEUR |
UK193AA |
Product preparation issue
Product preparation issue
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CMA only gave the diluent to the patient instead of combining it with the actual powdered Hib vaccin...
CMA only gave the diluent to the patient instead of combining it with the actual powdered Hib vaccine vial prior to administration.
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| 2849925 | 42 | M | AL | 07/16/2025 |
COVID19 COVID19 COVID19 COVID19 COVID19 COVID19 |
MODERNA MODERNA MODERNA MODERNA MODERNA MODERNA |
022M20A 022M20A 022M20A 045A21A 045A21A 045A21A |
Asthenia, Cardiac monitoring, Cardiac stress test, Dyspnoea, Echocardiogram; Fat...
Asthenia, Cardiac monitoring, Cardiac stress test, Dyspnoea, Echocardiogram; Fatigue, Heart rate irregular, Mitral valve incompetence, Palpitations, Tricuspid valve incompetence; Ultrasound scan, Ventricular extrasystoles; Asthenia, Cardiac monitoring, Cardiac stress test, Dyspnoea, Echocardiogram; Fatigue, Heart rate irregular, Mitral valve incompetence, Palpitations, Tricuspid valve incompetence; Ultrasound scan, Ventricular extrasystoles
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On 6 December 2021 I was overcome by an irregular heartbeat, fatigue, weakness, shortness of breath ...
On 6 December 2021 I was overcome by an irregular heartbeat, fatigue, weakness, shortness of breath and heart palpitations. I saw my primary caregiver who referred me to a cardiologist. After testing (Echocardiogram, sonogram, stress test and heart monitoring) it was determined that I had mild Mitral and Tricuspid Valve regurgitation with occasional unifocal PVC ( palpitations).
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| 2849926 | 2 | M | GA | 07/16/2025 |
PNC20 |
PFIZER\WYETH |
hh9322 |
Expired product administered, No adverse event
Expired product administered, No adverse event
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Expired vaccine was given, no adverse affect reported or seen by nurse in clinic
Expired vaccine was given, no adverse affect reported or seen by nurse in clinic
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| 2849927 | 56 | M | NC | 07/16/2025 |
HEP |
GLAXOSMITHKLINE BIOLOGICALS |
9K34M |
Dizziness, Dyspnoea, Flushing
Dizziness, Dyspnoea, Flushing
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pt became sob, dizzy, felt flushed a few min after vaccine, had already left clinical area and saw ...
pt became sob, dizzy, felt flushed a few min after vaccine, had already left clinical area and saw another team member while leaving. She noticed he did notlook like himself. she brough him to the office, put a fan on him, elevated his legs and he started feeling better. He left abruptly when he got a call from family member that his brother with dementia had wandered off and was missing. I did not have an opportunity to re-eval pt and no repeat vitals were taken.
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| 2849928 | 33 | M | VA | 07/16/2025 |
HEP |
GLAXOSMITHKLINE BIOLOGICALS |
K4JH7 |
Underdose
Underdose
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Patient was given pediatric dose instead of adult dose. Patient did not have an adverse reaction.
Patient was given pediatric dose instead of adult dose. Patient did not have an adverse reaction.
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| 2849929 | 16 | M | PA | 07/16/2025 |
MNQ |
NOVARTIS VACCINES AND DIAGNOSTICS |
U8169AB |
Eye pain
Eye pain
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Patient reports "severe right eye pain" that started when he woke up this morning. Patient...
Patient reports "severe right eye pain" that started when he woke up this morning. Patient mother called stating that the pain was worsening even with taking a dose of ibuprofen.
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| 2849930 | 62 | F | VA | 07/16/2025 |
VARZOS |
GLAXOSMITHKLINE BIOLOGICALS |
93N4J |
Feeling abnormal, Wrong product administered
Feeling abnormal, Wrong product administered
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Pt was to receive RSV vaccine on 7/9/2025. Nurse inadvertently administered Zoster vaccine instead....
Pt was to receive RSV vaccine on 7/9/2025. Nurse inadvertently administered Zoster vaccine instead. Pt has already had 2 doses of Shingrix. Pt reported on 7/12/25 that she had "felt icky" since 7/10/2025, but only mentioned having the standard reactions from receiving a Shingrix vaccine. Provider has discussed the patients concerns, and pt is no longer having any kind of symptoms from the vaccine.
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| 2849931 | 1 | M | MI | 07/16/2025 |
HEPA HIBV MMRV PNC20 VARCEL |
GLAXOSMITHKLINE BIOLOGICALS MERCK & CO. INC. MERCK & CO. INC. PFIZER\WYETH MERCK & CO. INC. |
DN273 Y008355 Y017204 LN4928 Y002062 |
Extra dose administered, No adverse event; Extra dose administered, No adverse e...
Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event
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Pt had no adverse reactions at time of vaccine administration. I told the provider what happened, ca...
Pt had no adverse reactions at time of vaccine administration. I told the provider what happened, called mom of the pt and let her know what happened, what to watch for. Called the health department and wasn't able to get ahold of anyone. I did send an email to vaccine contact at the health department.
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| 2849932 | 35 | M | AL | 07/16/2025 |
HEPA |
GLAXOSMITHKLINE BIOLOGICALS |
772yt |
Inappropriate schedule of product administration
Inappropriate schedule of product administration
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Dose administered at inappropriate time, should be at 6 months and was done at 39 days
Dose administered at inappropriate time, should be at 6 months and was done at 39 days
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| 2849933 | 35 | M | CA | 07/16/2025 |
TD |
MASS. PUB HLTH BIOL LAB |
A128A |
Arthralgia, Computerised tomogram normal, Oedema peripheral, X-ray normal
Arthralgia, Computerised tomogram normal, Oedema peripheral, X-ray normal
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pt states he had abnormal amount of shoulder pain that lasted for weeks after being vaccinated. It c...
pt states he had abnormal amount of shoulder pain that lasted for weeks after being vaccinated. It continues to hurt intermittently as the pain never goes away. There is some swelling in the armpit on the same side of the shoulder where he had his injection. It feels like a sore muscle and hurts. He is being treated at the VA having had x-ays and a CT both that were both negative so a MRI has been ordered that will be scheduled.
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| 2849934 | 15 | F | ND | 07/16/2025 |
HEPA HPV9 |
GLAXOSMITHKLINE BIOLOGICALS MERCK & CO. INC. |
J4K4X Z002903 |
Hypotonia, Pallor; Hypotonia, Pallor
Hypotonia, Pallor; Hypotonia, Pallor
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Client was visibly nervous and when asked stated she was ok getting shots. Gave both vaccinations in...
Client was visibly nervous and when asked stated she was ok getting shots. Gave both vaccinations in the right deltoid and client stated she was fine, with in minutes client became pale and put her head down and went limp. Client came to right away and I called for assistance from the administration assistant. We applied cold clothes the back of her neck and forehead. Client took a drink of water and then started vomiting. With minutes client passed out again. Instructed assistant to call 911 so she could be evaluated. Someone from the Ambulance department came from Social Services across the hall within minutes. I took client bp 103/67 pulse 86. Ambulance personnel assessed client and ambulance staff came and transported client to local ER to be further evaluated. Client stated she felt better and was able to ambulate to the ambulance. (withheld name)- RN
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| 2849935 | 50 | F | SC | 07/16/2025 |
HEP |
DYNAVAX TECHNOLOGIES CORPORATION |
945663 |
Alopecia
Alopecia
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Pt reported hair loss following the vaccine. She said that is has "slowed down" so she was...
Pt reported hair loss following the vaccine. She said that is has "slowed down" so she was ready to get her second dose. She stated she has researched and saw that it was a rare SE, and wanted to get the vaccine.
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| 2849936 | 0.17 | M | 07/16/2025 |
HEPA |
GLAXOSMITHKLINE BIOLOGICALS |
42DM9 |
No adverse event, Wrong product administered
No adverse event, Wrong product administered
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Using database, pulled a 2 month template that pulled Hepatitis A vaccine instead of Hepatitis B vac...
Using database, pulled a 2 month template that pulled Hepatitis A vaccine instead of Hepatitis B vaccine. MA verified with LVN who also did not notice Hep A vaccine, Hep A vaccine was given at 2 month WCC instead of Hepatitis B. Baby doing well this morning without adverse effects. Family informed and all questions answered
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| 2849937 | 10 | F | SC | 07/16/2025 |
MNQ MNQ |
SANOFI PASTEUR SANOFI PASTEUR |
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Computerised tomogram, Full blood count, Headache, Metabolic function test, Resp...
Computerised tomogram, Full blood count, Headache, Metabolic function test, Respiratory pathogen panel; Seizure
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Severe headaches since the vaccine. Had a siezure and was taken to the ER
Severe headaches since the vaccine. Had a siezure and was taken to the ER
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| 2849938 | 81 | M | MA | 07/16/2025 |
PNC21 |
MERCK & CO. INC. |
z002626 |
Pruritus
Pruritus
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Pt stated: "About 8 hours [after vaccine administration], I experienced intense itching in seve...
Pt stated: "About 8 hours [after vaccine administration], I experienced intense itching in several places, including my neck and arms. It was a VERY unusual sensation, almost electrical. It subsided after about 45 minutes, and didn't recur.
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| 2849939 | 0.17 | F | MN | 07/16/2025 |
DTPPVHBHPB PNC20 RV1 |
MSP VACCINE COMPANY PFIZER\WYETH GLAXOSMITHKLINE BIOLOGICALS |
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Rash; Rash; Rash
Rash; Rash; Rash
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Significant rash developed that was most consistent with eczema. Patient was seen in clinic for eval...
Significant rash developed that was most consistent with eczema. Patient was seen in clinic for evaluation. No threat to life.
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| 2849941 | 83 | M | 07/16/2025 |
UNK |
UNKNOWN MANUFACTURER |
3046732 |
Angioedema
Angioedema
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angioedema on 6/8/2025
angioedema on 6/8/2025
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| 2849942 | 75 | M | NC | 07/16/2025 |
PNC20 |
PFIZER\WYETH |
LN4929 |
Rash, Rash erythematous
Rash, Rash erythematous
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Patient given Prevnat 20 vaccine and started on glipizide at appt on 7/9/2025. Woke up on 7/10/2025...
Patient given Prevnat 20 vaccine and started on glipizide at appt on 7/9/2025. Woke up on 7/10/2025 with erythematous rash on upper arms. Glipizide was stopped. Rash has continued to progress since with areas on torso, proximal lower extremities, lots of white pustular lesions overlying erythematous base, widespread. No itching or pain. No fever or chills.
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| 2849943 | 0.08 | F | WA | 07/16/2025 |
DTPPVHBHPB DTPPVHBHPB DTPPVHBHPB DTPPVHBHPB PNC20 PNC20 PNC20 PNC20 RV5 RV5 RV5 RV5 |
MSP VACCINE COMPANY MSP VACCINE COMPANY MSP VACCINE COMPANY MSP VACCINE COMPANY PFIZER\WYETH PFIZER\WYETH PFIZER\WYETH PFIZER\WYETH MERCK & CO. INC. MERCK & CO. INC. MERCK & CO. INC. MERCK & CO. INC. |
U8313AA U8313AA U8313AA U8313AA MF0425 MF0425 MF0425 MF0425 2117047 2117047 2117047 2117047 |
Basophil count normal, Eosinophil count normal, Haematocrit decreased, Haemoglob...
Basophil count normal, Eosinophil count normal, Haematocrit decreased, Haemoglobin normal, Lymphocyte count normal; Lymphocyte percentage, Mean cell haemoglobin concentration normal, Mean cell haemoglobin normal, Mean cell volume normal, Mean platelet volume normal; Monocyte count normal, Monocyte percentage, Neutrophil count normal, Neutrophil percentage, Rash; Red blood cell count normal, Red cell distribution width normal, White blood cell count normal; Basophil count normal, Eosinophil count normal, Haematocrit decreased, Haemoglobin normal, Lymphocyte count normal; Lymphocyte percentage, Mean cell haemoglobin concentration normal, Mean cell haemoglobin normal, Mean cell volume normal, Mean platelet volume normal; Monocyte count normal, Monocyte percentage, Neutrophil count normal, Neutrophil percentage, Rash; Red blood cell count normal, Red cell distribution width normal, White blood cell count normal; Basophil count normal, Eosinophil count normal, Haematocrit decreased, Haemoglobin normal, Lymphocyte count normal; Lymphocyte percentage, Mean cell haemoglobin concentration normal, Mean cell haemoglobin normal, Mean cell volume normal, Mean platelet volume normal; Monocyte count normal, Monocyte percentage, Neutrophil count normal, Neutrophil percentage, Rash; Red blood cell count normal, Red cell distribution width normal, White blood cell count normal
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Rash that started on the face and moving onto the chest
Rash that started on the face and moving onto the chest
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| 2849944 | 12 | F | MI | 07/16/2025 |
HPV9 |
MERCK & CO. INC. |
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Headache
Headache
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Severe Headache
Severe Headache
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| 2849945 | 17 | M | MD | 07/16/2025 |
MENB |
NOVARTIS VACCINES AND DIAGNOSTICS |
2p77y |
Facial paralysis, Facial paresis, Headache, Hypoaesthesia, Hypoaesthesia oral
Facial paralysis, Facial paresis, Headache, Hypoaesthesia, Hypoaesthesia oral
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7/10 - Woke with headache in left parietal area. Mild/intermittent, occurring daily. Treated with ...
7/10 - Woke with headache in left parietal area. Mild/intermittent, occurring daily. Treated with Ibuprofen 600 mg. 7/14 - Began with numbness and weakness on the left side of face. Progressed with left sided facial drooping and numbness on left side of the tongue. Treated with Prednisone 20 mg 3 pills daily for 6 days followed by 2 pills daily for 3 days and 1 pill daily for 3 days.
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| 2849946 | 13 | M | MI | 07/16/2025 |
TDAP |
GLAXOSMITHKLINE BIOLOGICALS |
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Abdominal pain upper, Diarrhoea, Vomiting
Abdominal pain upper, Diarrhoea, Vomiting
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Patient had severe bout of vomiting followed by diarrhea for 2 hours on 7/10/24. Patient vomited mu...
Patient had severe bout of vomiting followed by diarrhea for 2 hours on 7/10/24. Patient vomited multiple times on 4 occasions, had stomach cramping, and then experienced diarrhea. These events occurred between 12:45pm - 2:45pm. No other symptoms noted.
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| 2849947 | 67 | F | IL | 07/16/2025 |
VARZOS |
GLAXOSMITHKLINE BIOLOGICALS |
93n4j |
Injection site bruising, Injection site pruritus, Injection site urticaria, Prur...
Injection site bruising, Injection site pruritus, Injection site urticaria, Pruritus
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According to patient two hours after immunization, the patient began experiencing itchiness at the ...
According to patient two hours after immunization, the patient began experiencing itchiness at the injection site. By the end of the day patient had itchiness all over the body and hives on the injection site and took Benadryl for it. Patient does not suffer from itchiness, but injection site is still bruised
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| 2849948 | 0.33 | F | NV | 07/16/2025 |
HEP |
MERCK & CO. INC. |
Y014090 |
Inappropriate schedule of product administration
Inappropriate schedule of product administration
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PT was accidentally administered Hep B to early
PT was accidentally administered Hep B to early
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| 2849949 | 1.25 | M | LA | 07/16/2025 |
PNC20 |
PFIZER\WYETH |
LN4931 |
Extra dose administered, No adverse event
Extra dose administered, No adverse event
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He was getting vaccines at 15 month well check. Mother has elected to space out vaccines, so schedu...
He was getting vaccines at 15 month well check. Mother has elected to space out vaccines, so schedule is altered, He got MMR and Prevnar at 12 month well. Prevnar vaccine was given today in clinic- it was an additional dose that he did not need/off schedule. No problems noted after vaccine was given. Baby has had no adverse effects.
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| 2849950 | 80 | M | 07/16/2025 |
RSV |
PFIZER\WYETH |
MD5462 |
Atrial flutter, Chills, Pyrexia
Atrial flutter, Chills, Pyrexia
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Patient received the vaccine. 30 minutes later he developed chills, fever, rigors and afib with rvr.
Patient received the vaccine. 30 minutes later he developed chills, fever, rigors and afib with rvr.
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| 2849951 | 65 | F | 07/16/2025 |
VARZOS |
GLAXOSMITHKLINE BIOLOGICALS |
58160-0823-11 |
Headache, Rash
Headache, Rash
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Rash for 2 weeks and headache couple days
Rash for 2 weeks and headache couple days
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| 2849952 | 54 | F | 07/16/2025 |
PNC20 PNC20 |
PFIZER\WYETH PFIZER\WYETH |
LN4930 LN4930 |
Body temperature increased, Chills, Fatigue, Hyperhidrosis, Injection site eryth...
Body temperature increased, Chills, Fatigue, Hyperhidrosis, Injection site erythema; Nausea, Neck pain, Rhinorrhoea
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Got prevnar on 7/10/2025--2:30 am--nausea, fatigue. Chills. ? Temp. Sweats. Rhinorrhea--last 48 hou...
Got prevnar on 7/10/2025--2:30 am--nausea, fatigue. Chills. ? Temp. Sweats. Rhinorrhea--last 48 hours. Right neck pain. Redness to arm where prevnar was given. No numbness to the arm. No cough. No SOB. No lower GI symptoms. Tylenol / motrin recommended
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| 2849953 | 73 | M | AL | 07/16/2025 |
COVID19 COVID19 |
MODERNA MODERNA |
052E21A 052E21A |
Cardiac function test, Cardiac perfusion defect, Dizziness, Dyspnoea, Electrocar...
Cardiac function test, Cardiac perfusion defect, Dizziness, Dyspnoea, Electrocardiogram; Fatigue, Gait disturbance
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Normally a morning runner with 3-5 miles/ day. Just over 2 weeks past the Covid Booster shot (had th...
Normally a morning runner with 3-5 miles/ day. Just over 2 weeks past the Covid Booster shot (had the initial 2 shots) I was so fatigued I could not walk up the hill I run every day. Tried it multiple times over the next couple of days with the same effect. As a former mini Triathlon winner I was in very good shape and ran every day. The fatigue, in ability to breath, dizzy, and light headed was a totally new experience. I set up an appointment with personal physician for 10+ years and he set up a visit with Cardiologist. Ran a series of stress tests, EKG and other cardiac tests. Reported Cardiac Perfusion Defect.
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| 2849954 | 1.92 | M | OK | 07/16/2025 |
DTAPIPVHIB HEPA MMR PNC15 VARCEL |
SANOFI PASTEUR GLAXOSMITHKLINE BIOLOGICALS MERCK & CO. INC. MERCK & CO. INC. MERCK & CO. INC. |
UK174AB J4K4X Y008592 Y010035 Y019319 |
Erythema, Pruritus, Urticaria; Erythema, Pruritus, Urticaria; Erythema, Pruritus...
Erythema, Pruritus, Urticaria; Erythema, Pruritus, Urticaria; Erythema, Pruritus, Urticaria; Erythema, Pruritus, Urticaria; Erythema, Pruritus, Urticaria
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Client began scratching neck shortly after vaccines while waiting in the lobby. Redness/welts noted...
Client began scratching neck shortly after vaccines while waiting in the lobby. Redness/welts noted to back of neck and waistline. Client also noted to have diffuse reddened welts to back. Client was in no distress and no airway distress noted. 911 was called and client was transported to (withheld name) Hospital. Client discharged home from ER per mother.
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| 2849955 | 1.33 | F | VT | 07/16/2025 |
DTPPVHBHPB |
MSP VACCINE COMPANY |
U7970BA |
Wrong product administered
Wrong product administered
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Pt was accidently given Vaxelis when they were supposed to just get HIB
Pt was accidently given Vaxelis when they were supposed to just get HIB
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| 2849956 | 4 | F | OH | 07/16/2025 |
DTAP |
SANOFI PASTEUR |
3CA20C1 |
Injection site erythema, Injection site reaction, Injection site swelling, Injec...
Injection site erythema, Injection site reaction, Injection site swelling, Injection site warmth, Urticaria
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Within 24 we were notified by daycare provider that her injection site might need to be looked at. A...
Within 24 we were notified by daycare provider that her injection site might need to be looked at. At first it was about a 1 inch diameter red circle. After 48 hours the reaction had grown to over 5 inches in diameter, became red, hot, and swollen. At 60 hours there were signs of welts within the red circle.
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| 2849957 | 17 | F | MN | 07/16/2025 |
MENB MENB |
PFIZER\WYETH PFIZER\WYETH |
lw8911 lw8911 |
Blood magnesium, Electrocardiogram, Full blood count, Headache, Human chorionic ...
Blood magnesium, Electrocardiogram, Full blood count, Headache, Human chorionic gonadotropin; Lipase, Liver function test, Metabolic function test, Syncope
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Headache, syncope
Headache, syncope
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| 2849958 | 102 | F | FL | 07/16/2025 |
RSV |
GLAXOSMITHKLINE BIOLOGICALS |
255T2 |
Extra dose administered, No adverse event
Extra dose administered, No adverse event
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Patient received the RSV vaccine 04/2024 at a pharmacy in (withheld state). She received the RSV vac...
Patient received the RSV vaccine 04/2024 at a pharmacy in (withheld state). She received the RSV vaccine again on 07/15/2025 at pharmacy in (withheld different state). Her vaccine record was not in the (withheld state) Immunization Registry and our default transaction history goes back one year (unless you manually change the year to go back farther). When the pharmacist check data base and the default one year transaction history it seemed as if the patient had never received the RSV vaccine. The patient did not remember that she had already received it. I spoke with her 07/16/2025 and she is fine/doing well with no adverse events.
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| 2849959 | 36 | M | FL | 07/16/2025 |
COVID19 |
MODERNA |
054C21A |
Computerised tomogram, Diverticulitis
Computerised tomogram, Diverticulitis
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Diverticulitis
Diverticulitis
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| 2849960 | 32 | F | TX | 07/16/2025 |
MMR VARCEL |
MERCK & CO. INC. MERCK & CO. INC. |
Y007613 z003883 |
Injection site erythema, Injection site swelling, Pyrexia, Urticaria; Injection ...
Injection site erythema, Injection site swelling, Pyrexia, Urticaria; Injection site erythema, Injection site swelling, Pyrexia, Urticaria
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Patient had redness, swollen at site of vaccine. Patient also had fever, hives on her body.
Patient had redness, swollen at site of vaccine. Patient also had fever, hives on her body.
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| 2849961 | 70 | F | VA | 07/16/2025 |
PNC21 |
MERCK & CO. INC. |
Y019158 |
Myalgia, Pain, Pain in extremity
Myalgia, Pain, Pain in extremity
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Patient received Capvaxive vaccine on 6/23/2025 in her right deltoid, was monitored for 15 minutes a...
Patient received Capvaxive vaccine on 6/23/2025 in her right deltoid, was monitored for 15 minutes afterward and tolerated immunization administration well. She states she developed mild arm pain that evening, which has persisted since that time, for approximately 23 days. She has taken ibuprofen with some relief. She reports the pain is localized to the muscle, and hurts when raising her right arm off a table. She denies any signs of infection, including redness, swelling, warmth, or fever. Advised patient to try alternating acetaminophen and ibuprofen, apply warm or cold compresses as needed, offered patient appointment to be seen today or tomorrow and she is unable to come in. Discussed other evaluation opportunities with patient, and she plans to go to a walk in orthopedics clinic this week for evaluation.
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