- Staat
- GA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 03.05.2023
- Impfdatum
- 01.03.2023
- Beginn
- 02.03.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Catheterisation cardiac abnormal
Chest pain
Condition aggravated
Coronary angioplasty
Myocardial infarction
Symptomtext
Approximately 22 hours after getting vaccinated, started having chest pain in the middle of chest. Checked BP couple hours later, 215/110, decided to go to ER. Admitted to step down unit on 3/2/23. About 5 am on 3/3/23 started having heart attack. Had heart cath same day and "they used a balloon to open the stents that were originally placed in 2016". Released from hospital on 3/6/23 to follow up with cardiologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- IDDM, hypertension, neuropathy, cardiac stents, hx of heart attack
- Andere Medikamente
- Aspirin, Toprol, Losartin, Pravastatin, Tramadol, Gabapentin, Cymbalta, Amlodipine, Novolog
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 16.04.2023
- Impfdatum
- 04.04.2023
- Beginn
- 04.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Anaphylactic reaction
Arthralgia
Asthenia
Autoimmune disorder
Bell's palsy
Blood disorder
Cardiac disorder
Cerebrovascular accident
Chest discomfort
Chest pain
Chills
Confusional state
Diarrhoea
Dizziness
Dysphagia
Dyspnoea
Eye swelling
Symptomtext
Site: Bruising at Injection Site-Severe, Site: Itching at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Allergic: Anaphylaxis-Severe, Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Severe, Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Allergic: Itch Generalized-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash Generalized-Severe, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Severe, Systemic: Abdominal Pain-Severe, Systemic: Autoimmune Disease (diagnosed by MD)-Severe, Systemic: Bell's Palsy-Severe, Systemic: Blood Disorder (diagnosed by MD)-Severe, Systemic: Body Aches Generalized-Severe, Systemic: Cardiac Disorder (diagnosed by MD)-Severe, Systemic: Chest Tightness / Heaviness / Pain-Severe, Systemic: Chills-Severe, Systemic: Confusion-Severe, Systemic: Diarrhea-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Fever-Severe, Systemic: soreness that was from the anterior deltoid to the interior of the elbow-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Headache-Severe, Systemic: Heart Attack-Severe, Systemic: Hypertension-Severe, Systemic: Hyperventilation-Severe, Systemic: Hypotension-Severe, Systemic: Joint Pain-Severe, Systemic: Lymph Node Swelling-Severe, Systemic: MIS (Multisystem Inflammatory Syndrome)(diagnosed by MD)-Severe, Systemic: Nausea-Severe, Systemic: Neurological Disorder (diagnosed by MD)-Severe, Systemic: Numbness (specify: facial area, extremities)-Severe, Systemic: Seizure-Severe, Systemic: Shakiness-Severe, Systemic: Stroke-Severe, Systemic: Tachycardia-Severe, Systemic: Tingling (specify: facial area, extemities)-Severe, Systemic: Tinnitus-Severe, Systemic: Unable to Sleep-Severe, Systemic: Visual Changes/Disturbances-Severe, Systemic: Vomiting-Severe, Systemic: Weakness-Severe, Additional Details: no pain at injection, but anterior and not pain, but a soreness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 04.08.2023
- Impfdatum
- 04.08.2023
- Beginn
- 04.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Flushing
Loss of consciousness
Snoring
Syncope
Symptomtext
Within 2 seconds of administration, pt had a syncopal episode. Facial flushing was present, +LOC occurred, pt was heavily snoring for approximately 20 seconds, then regained consciousness without medical intervention. Vital Signs were stable, BP 112/74, HR 85, O2 99%; no treatment performed other than continuous visual monitoring for 15 minutes after vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 26.07.2023
- Impfdatum
- 25.07.2023
- Beginn
- 25.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fall
Nausea
Syncope
Symptomtext
As patient was leaving the vaccination site, patient had a syncopal episode resulting in fainting. Dad was present during the fall. Patient reported feeling dizzy, lightheaded, and nauseous (no emesis). Patient breathing was not compromised. We observed patient for about 15 minutes. Water was provided and school staff gave her some Popsicles. Patient's parent reported patient did not eat prior to vaccination and was also out in the sun/heat for about 30 minutes in the registration line. Obtained vitals prior to patient being discharged home with parent. SpO2: 98, HR: 74, BP: 110/70. Patient recovered well and went home with no further issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 10.05.2023
- Impfdatum
- 10.05.2023
- Beginn
- 10.05.2023
- 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
Loss of consciousness
Pallor
Supine position
Symptomtext
Within 3-5 minutes of receiving the vaccine, patient stated they felt lightheaded and dizzy. Patient lost consciousness shortly after for approximately 30 seconds and their face became pale. Patient was brought to a supine position with legs elevated until color returned and she regained consciousness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Singulair
- Allergien
- Shellfish, Tree Nuts, Bee Stings, Propanolol
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 28.04.2023
- Impfdatum
- 19.04.2023
- Beginn
- 19.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Syncope
Symptomtext
SYNCOPE IN SEATED POSITION 1 MINUTE AFTER SECOND VACCINE GIVEN. PT WAS EASED TO A LAYING POSITION. SHE REGAINED FULL CONCIOUSNESS IN 1 MINUTE, SHE EXPLAINED SHE HAD NOT EATEN ALL DAY AND HAD JUST RETURNED FROM GYM AFTER A MODERATE WORKOUT. SHE WAS GIVEN A BOTTLE OF WATER TO DRINK AND REMAINED IN CLINIC FOR 30 MINUTES. DURING THIS TIME, SHE HAD NO RASHES, COUGHING, HIVES, SOA, NOR DID SHE GET NAUSEAUS. SHE WAS LAUGHING AND STATED SHE FELT FINE IN ALL RESPECTS . AFTER 10 MINUTES I GAVE HER A CANDY BAR WHICH SHE SAID MADE HER FEEL BETTER STILL . SHE LEFT WITH A FRIEND WHO WAS PRESENT WHO DROVE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- FLONASE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 20.04.2023
- Impfdatum
- 17.04.2023
- Beginn
- 18.04.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Movement disorder
Paralysis
Symptomtext
patient states unable to move with paralysis for approximately 6 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure and cholesterol
- Andere Medikamente
- jardiance, carvedilol, rosuvastatin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 01.04.2023
- Impfdatum
- 01.04.2023
- Beginn
- 01.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Syncope
Vision blurred
Symptomtext
After all the vaccines were administered the patient started to have blurred vision and cold sweats, a few minutes after he faint. We monitor his pulse and call EMS. when paramedics arrived, patient was alert, and all vital signs were normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- chronic heart diseases and htn
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 30.03.2023
- Impfdatum
- 07.03.2023
- Beginn
- 07.03.2023
- 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
Cryotherapy
Discomfort
Dizziness
Exposure during pregnancy
Immediate post-injection reaction
Inflammation
Injected limb mobility decreased
Injection site pain
Injection site reaction
Insomnia
Loss of consciousness
Loss of personal independence in daily activities
Muscle spasms
Muscular weakness
Pain
Presyncope
Product administered at inappropriate site
Symptomtext
Adverse event(): Following the administration of the Tdap vaccine near her shoulder, the patient experienced a transient blackout, feelings of faintness, blurred and black vision, and ringing in the ears. The healthcare provider administering the vaccine quickly left the patient unattended at this time, having gone to another room to grab a bandage. The patient was not supervised during that time but was also not inquired about her well-being despite almost fainting. The name we were given for the nurse who administered the vaccine. The patient was advised that pain associated with the Tdap vaccine is common and should resolve within a few days. However, despite trying Tylenol and ice as that doctor's office suggested, the pain persisted. Upon returning to the same Gynecologist's office, they would not attribute the pain to the vaccine administration and did not file a VAERS report themselves despite the difficult situation my wife is going through because of the error in vaccine administration. The patient had no prior history of pain or issues with her arm, and the discomfort began immediately after the vaccine administration. The patient then sought care from a different gynecology office and consulted a chiropractor/therapist. It was determined that the patient had left infraspinatus and supraspinatus tendonitis, left anterior deltoid weakness, and left trap muscle spasms, all resulting from the vaccine being administered in the wrong location. More details are in the medical test/report secion. The chiropractor mentioned that this occured because vaccine was administered in the the wrong spot and directly hit the patients tendon, leading to severe inflammation and worsening pain over time. The patient, who is in the final weeks of her pregnancy, has visited the physical therapist multiple times for treatment, but the pain has not improved. Icing the affected area has become increasingly painful, causing the patient to scream in agony. Due to the late stage of her pregnancy, she has been advised against taking any medication or undergoing an MRI scan by multiple doctors to further analyze the issue but plans to do so after giving birth. The patient is struggling to sleep due to persistent pain and has had considerable difficulty caring for her son and performing household tasks. As a result, her spouse has had to take time from work to provide assistance. The family is concerned that the negligence in administering the vaccine will also affect the patient's ability to care for the newborn. In summary, the adverse event following the Tdap vaccine administration has led to significant pain, inflammation, and functional limitations for the patient. Despite seeking treatment from a physical therapist, her condition has not improved. The ongoing pain has impacted her daily life, raising concerns about her well-being and ability to care for her family, particularly with the imminent arrival of a new child. The patient plans to have an MRI scan after giving birth to investigate the issue further and determine the appropriate course of action for recovery. Treatment: The patient has received multiple treatments from the chiropractor, including ultrasound, soft tissue work, cryotherapy, ice application, and stretching exercises. However, the pain and inflammation continue to worsen. Outcome(s): The patient's pain and inflammation have not improved, making it difficult for her to perform daily tasks, care for her child, and sleep. She is in the final weeks of pregnancy and has been advised against getting on shots or getting an MRI to further analyze the issue. The ongoing pain and discomfort are expected to affect her ability to care for her newborn. Pregnancy history: The patient is currently in the final weeks of her pregnancy with estimated delivery date of 05/05/2023. This is the second pregnancy Birth weight is not yet available
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- 1. Date: March 18, 2023 Provider: Chiropractor Exam findings: Patient reported Tdap vaccine received on March 7, 2023, with persistent pain since then; left medial deltoid pain, decreased left shoulder adduction, pain during various activities, left anterior deltoid weakness, left infraspinatus and left supraspinatus tendonitis, left trap muscle spasms, T2/4/5 post TP on right, T3/5/7 post TP on left, tendonitis in insertion of the left supraspinatus at the lesser tuberosity of the humerus, and left infraspinatus tendons at its insertion at the left greater tuberosity of the humerus. Treatment: History and exam of left shoulder, ultrasound to left deltoid muscle for 10 minutes, soft tissue work to left deltoid and left trap muscle for 10 minutes, adjusted T-sp light div. 2. Date: March 20, 2023 Provider: Chiropractor Exam findings: Patient still experiencing the same pain in her left shoulder following Tdap vaccine; left infraspinatus tendonitis and left trap muscle spasm. Treatment: Ultrasound for a few minutes (discontinued due to pain), cryotherapy and ice application, light biofreeze and frankincense applied to the left infraspinatus muscle, and PNF stretching for left trap muscles. Patient is continuing to go for treatment. Treatment options are very limited due to patients condition
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Prenatal Multivitamin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 24.09.2023
- Beginn
- 25.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye swelling
Migraine
Pyrexia
Swelling of eyelid
Symptomtext
Severe eye swelling underneath and lids, migraines and fever of 103 degrees within 18 hours of injection. Symptoms lasted for 2-3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Armour Thyroid
- Allergien
- red wine, Pepto Bismol, Aspirin, Miralax , Tubersol, Demerol
- Vorherige Impfungen
- Severe swelling of entire arm from Tuberculin PPD at 30 years old in 2010, Sanofi P
- Staat
- OK
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 22.09.2023
- Impfdatum
- 18.09.2023
- Beginn
- 19.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Pain in extremity
Peripheral swelling
Sleep disorder
Swelling
Tenderness
Symptomtext
Arm swollen, has a visible raised area, hurts to raise the arm, tender and aching enough to lose sleep. Treatment recommendations by her physician was to take some Advil and call the pharmacy. Treatment recommendations by the pharmacy was to add cold packs throughout the day, monitor and call physician/urgent care for visit if not better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hashimoto's Disease Chronic back pain
- Andere Medikamente
- Synthroid every day, that is all.
- Allergien
- Latex Percocet
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 30.05.2023
- Impfdatum
- 29.03.2023
- Beginn
- 30.03.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cardiac stress test normal
Chest pain
Dyspepsia
Electrocardiogram normal
Hypertension
Symptomtext
chest pain and heartburn for 5 days, high blood pressure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- ECG--normal sinus rhythm with inferior infarct, age unknown--04/03/2023 Stress EKG test--normal sinus rhythm with no significant ST or T-wave changes--no arrhythmias--HBP--04/18/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Seasonal allergies, hypertension, hyperlipidemia, kidney stones, osteoarthritis
- Andere Medikamente
- Lisinopril 5 mg, Chlorthalidone (1/2 )25 mg, magnesium bisglycinate chelate and magnesium oxide 133 mg, loratadine 10 mg, coenzyme Q10 - 100 mg, omega 3 fish oil, vitamin D & K2- 2000 IU, psyllium, vitamin B complex, probiotic, CBD topical
- Allergien
- iodine, Septra, Vicodin, Amantadine, seasonal allergies
- Vorherige Impfungen
- Sore arm for 3 months, age 60, 11/10/21 & 11/14/22, Covid19 Moderna Bivalent,
- Staat
- CO
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 27.04.2023
- Impfdatum
- 23.03.2023
- Beginn
- 24.03.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Depression
Ear pain
Headache
Hypertension
Musculoskeletal stiffness
Vertigo positional
Symptomtext
Per office note of 4/26/23 of Dr: Patient states the next day she woke up with a very bad headache and stiff neck that she initially thought were reactions to the vaccinations. She then started having issues with her ears and ear pain, which she thought was an ear infection. When she lays down at night she get a bit of vertigo. Her blood pressure has been high again, which she states it has not been high in 10-15 years. At the time she was getting the vaccines she also had increased the dose of antidepressants.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- amlodipine 5 mg daily, atenolol 50 mg daily, citalopram 40 mg daily, Efudex 5% cream bid, fluoxetine 20 mg 3 caps daily, losartan-HCTZ 100/25 mg daily, trazadone 50 mg at he
- Allergien
- lisinopril tramadol
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 13.07.2023
- Impfdatum
- 10.07.2023
- Beginn
- 10.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Incoherent
Vomiting
Symptomtext
5 Minutes after giving patient Vaccines the patient started to vomit, dizzy, and was a little coherent for like 10 minutes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 06.07.2023
- Impfdatum
- 26.06.2023
- Beginn
- 26.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash pruritic
Symptomtext
Patient starting getting an itchy rash on 7/4/23. Rash is on forearms and neck is also itching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Allergy to eggs and patient said she is eating farm fresh eggs now.
- Andere Medikamente
- mobic, phentermine, zoloft, glucophage xr, folic acid, lisinopril, topiramate, atorvastatin
- Allergien
- corn, eggs, lactose, tramadol
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 14.06.2023
- Impfdatum
- 13.06.2023
- Beginn
- 13.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Pruritus
Rash
Symptomtext
The patient reports that yesterday evening after the vaccine she experienced itching and a rash on her ankle. Today the rash has gotten worse and is appearing on both legs and is spreading to the rest of her legs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 05.06.2023
- Impfdatum
- 22.05.2023
- Beginn
- 28.05.2023
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Erythema
Pain in extremity
Symptomtext
Patient states that on 5/22/2023 he was at medical facility for an evaluation and was due for a Tdap vaccine, patient received the Tdap vaccine on that date. Patient reports he initially had soreness in the left arm and several days later noticed a blister had developed and "popped". Patient self treated blister with Neosporin ointment. Patient noticed area was reddened at worsening on 5/28/2023 and called medical facility on 5/30/2023 to report issue. Patient was seen on 5/30/2023 and was started on oral antibiotics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 30.05.2023
- Impfdatum
- 11.05.2023
- Beginn
- 13.05.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injection site bruising
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Site: Bruising at Injection Site-Mild, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 24.05.2023
- Impfdatum
- 16.05.2023
- Beginn
- 22.05.2023
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Urticaria
Symptomtext
Father of patient presented to Immunizations and stated his son developed hives on the back of both thighs despite receiving injections in both deltoids. Father stated no changes in routine such as changing soaps/detergents and stated no issues previously from vaccines. Father stated rash being treated with hydrocortisone and is improving, no pain or itchiness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.05.2023
- Impfdatum
- 01.04.2023
- Beginn
- 01.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Blister
Herpes zoster
Pain in extremity
Rash
Erythema
Swelling
Symptomtext
Worst case of Shingles, getting worse, been at Dr,; This non-serious case was reported by a consumer via call center representative and described the occurrence of shingles in a patient who received Herpes zoster (Shingrix) for prophylaxis. In APR-2023, the patient received Shingrix (unknown arm). In APR-2023, 1 week after receiving Shingrix, the patient experienced shingles (Verbatim: Worst case of Shingles, getting worse, been at Dr,). The outcome of the shingles was not resolved. It was unknown if the reporter considered the shingles to be related to Shingrix. It was unknown if the company considered the shingles to be related to Shingrix. Additional Information: GSK Receipt Date: 27-APR-2023 The case was self reported by the patient. The patient received the Shingrix vaccine three weeks ago and a week later he/she got the worse case of shingles. The patient had been to the doctor twice and things were getting worse. The pharmacist gave him/her another vaccine at the same arm at the same time, at pharmacy and the patient understanding now what he did was wrong.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 01.05.2023
- Impfdatum
- 25.04.2023
- Beginn
- 26.04.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site rash
Injection site swelling
Lymphadenopathy
Malaise
Rash
Rash erythematous
Rash vesicular
Symptomtext
Left upper arm pain and swelling. Left axillary lymphadenopathy. Vesicular rash in axilla. Another patchy, erythematous rash on left upper arm. General malaise.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- GERD, vomiting
- Vorgeschichte
- OSA on CPAP HTN GERD PTSD
- Andere Medikamente
- Lisinopril 10mg daily Omeprazole 40mg daily
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 22.04.2023
- Impfdatum
- 20.04.2023
- Beginn
- 21.04.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pain
Wrong technique in product usage process
Symptomtext
Patient was not happy when noticed little air left inside Boostrix syringe as pharmacist didn't pull the plunge all the way to the upper most level before injection, she thinks some air injected into her "vein:" that caused her pain and possibly injury.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 18.03.2023
- Beginn
- 31.03.2023
- Tage bis Beginn
- 13,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain
Pruritus
Swelling
Symptomtext
Patient came to pharmacy on 03/31/2023 and informed that she had redness,bump and swelling after she got the boostrix vaccine on 03/18/2023 which became worst after 4 days. It was itchy, painful and swollen. Now she is getting better, but she is still a little itchy, has redness and some pain. Patient also informed me that the redness traveled down her arm. Recommended patient to see a doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 27.03.2023
- Beginn
- 27.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Tendonitis
Symptomtext
patient stated severe arm pain started 4 hours after the vaccine tendonitis feeling patient was seen in followup app't on March 30, 2023 with Dr.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- prenatal vitamin
- Allergien
- No Known Drug allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 25.03.2023
- Beginn
- 27.03.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Pain
Pain in extremity
Symptomtext
Patient experienced numbness and arm pain on the day of the vaccination. On March 27th patient called the pharmacy and complained of numbness and pain that she felt radiated down to her legs when she woke up that morning. At the time of conversation around 1pm she said the symptoms are starting to fade and is not as bad as it was that morning. Pharmacist advised her to call her doctor and report the ADR so she can be checked if necessary.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Migraine headache Asthma
- Vorgeschichte
- Unknown
- Andere Medikamente
- Augmentin, Trazodone, Effexor
- Allergien
- Depakote, Nicotine, Tylenol
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 27.03.2023
- Impfdatum
- 22.03.2023
- Beginn
- 22.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
LEFT ARM - RED AND SWOLLEN ON SITE OF INJECTION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 17.03.2023
- Impfdatum
- 09.03.2023
- Beginn
- 10.03.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash vesicular
Symptomtext
Patient described a rash on her Torso along chest and arms. It was red, bumpy with blisters. It began soon after the vaccines and continues 2 weeks later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- OTC - Unknown Tramadol, zonisamide, folic acid, singulair, zyrtec, leflunamide, etodolac
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 15.03.2023
- Impfdatum
- 15.03.2023
- Beginn
- 15.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Pulse abnormal
Unresponsive to stimuli
Symptomtext
One to two minutes after shot patient complained of seeing stars (light-headed) and felt nauseous. Several minutes later the patient became unresponsive with eyes still open for around 2 minutes at which time EMS was called. She was sweating profusely and had a week pulse. The paramedics responded and checked her out. They okayed her to leave with her husband after she was feeling better (15-20 minutes later) and there was NO transportation to the hospital needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No known illnesses
- Vorgeschichte
- No known health conditions
- Andere Medikamente
- Unknown
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 07.12.2023
- Impfdatum
- 05.09.2023
- Beginn
- 05.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
Patient was at clinic for Meningococcal vaccine and was given PSV23 instead. She has no high risk indicators for PSV23 at this time. 12/7/2023 Mom notified and denies any reaction after vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 6,0
- Geschlecht
- F
- Eingang
- 17.11.2023
- Impfdatum
- 17.11.2023
- Beginn
- 17.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Patient was given the wrong vaccine. Patient was due for Dtap and was given TDAP .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- None. Spoke with State Vaccine Unit and they advised us that patient doesn't need to repeat the vaccine and the series is complete, Patient will due for the next dose when she's 11-12 years old. Parents made aware
- Aktuelle Erkrankungen
- None at the time of vaccination. Upper respiratory infection on 11/03/2023
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 26.09.2023
- Impfdatum
- 28.08.2023
- Beginn
- 28.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 26.09.2023
- Impfdatum
- 25.08.2023
- Beginn
- 25.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 20.09.2023
- Impfdatum
- 23.08.2023
- Beginn
- 23.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 7,0
- Geschlecht
- F
- Eingang
- 19.09.2023
- Impfdatum
- 23.08.2023
- Beginn
- 23.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 8,0
- Geschlecht
- M
- Eingang
- 19.09.2023
- Impfdatum
- 23.08.2023
- Beginn
- 23.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 19.09.2023
- Impfdatum
- 23.08.2023
- Beginn
- 23.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 31.08.2023
- Impfdatum
- 30.08.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Patient received ProQuad and Varivax on same day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 31.08.2023
- Impfdatum
- 30.08.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Patient received ProQuad and Varivax on same day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 24.08.2023
- Impfdatum
- 11.08.2023
- Beginn
- 20.08.2023
- Tage bis Beginn
- 9,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Basophil percentage
Blast cells absent
Blood albumin normal
Blood lactate dehydrogenase increased
Blood urine present
C-reactive protein
Eosinophil percentage increased
Full blood count abnormal
Granulocyte percentage
Haemoglobin normal
Immune thrombocytopenia
Immunoglobulin therapy
Lymphocyte percentage
Monocyte count increased
Platelet count decreased
Platelet morphology abnormal
Protein urine present
Red blood cell sedimentation rate increased
Symptomtext
Developed ITP for which he was admitted to the hospital on 8/22/23, received IVIG and started on steroids. Will follow-up with Heme/Onc.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Basophil percentage
- Hospital-Tage
- 1,0
- Labordaten
- 8/21/23: strep positive at urgent care 8/22/23 initial labs in clinic: CBC with plt count of 1K , mono# 1.0, Gran 59.5%, lymph 22.7%, eos 5.5%, plts decreased and giant platelets present; UA with blood and protein; albumin 4.8; ESR 20; CRP 1.0. 8/22/23 repeat labs in hospital: path smear with severe thrombocytopenia, normal hgb, normal leukocytes with mostly unremarkable differential and morphology, NO blasts; repeat cbc with mono# 0.9, eos 5.8%, baso 0.8%, decreased platelets; LDH 320; albumin 4.8; 8/23/23: after IVIG; repeat UA normal. repeat CBC with plt count 52K still with decreased plts; eos 6.4%
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- albuterol PRN cetirizine PRN Flonase PRN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 08.08.2023
- Impfdatum
- 07.08.2023
- Beginn
- 08.08.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
patient was scheduled on nurse visit and Medical Assistant looked at note in chart for order to give vaccines. Medical assistant misread the providers previous note as the note for current visit and inadvertently gave repeat of previous vaccines. Patient received Tdap, varicella on 7/27/23 and again on 8/5/23. In addition patient did receive HPV which was correct as ordered. No adverse reaction has occurred at this time and provider disclosed information with patient and family.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 24.07.2023
- Impfdatum
- 14.07.2023
- Beginn
- 14.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
NO ADVERSE EVENT NOTED OR REPORTED. PT MISTAKENLY GIVEN COMBINATION MMRV VACCINE INSTEAD OF SEPARATE MMR AND VARICELLA VACCINES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- F
- Eingang
- 28.06.2023
- Impfdatum
- 19.06.2023
- Beginn
- 19.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Extra dose given; Extra dose given; This non-serious case was reported by a nurse via call center representative and described the occurrence of extra dose administered in a 12-year-old female patient who received DTPa (Reduced antigen) (Boostrix) (batch number B32NG, expiry date 13-JUN-2025) for prophylaxis. Co-suspect products included Men ACWY-CRM NVS (Menveo) (batch number AMVA912A, expiry date 30-MAR-2024) for prophylaxis. Previously administered products included Boostrix (1st dose received on 14th June 2022 with batch number C5788BA and expiry date 14th October 2022) and Menveo (1st dose received on an unknown date with batch number AMVA659A and expiry date 30th January 2023). On 19-JUN-2023, the patient received the 2nd dose of Boostrix. On an unknown date, the patient received the 2nd dose of Menveo. On 19-JUN-2023, an unknown time after receiving Boostrix and not applicable after receiving Menveo, the patient experienced extra dose administered (Verbatim: Extra dose given). On an unknown date, the patient experienced extra dose administered (Verbatim: Extra dose given). The outcome of the extra dose administered and extra dose administered were unknown. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 22-JUN-2023 A nurse called in to report that a patient accidentally received a second dose of Boostrix and Menveo one year after the first dose and wished to know how to proceed. The information for both doses was given, including lot number, expiration date, patient information and vaccination event. The vaccine administration facility was the same as primary reporter. The information for Menveo was provided by a Menveo second line agent after the call was escalated. The reporter consented to follow up. The patient received second dose of Boostrix and Menveo one year after first dose, which led to extra dose administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 22.06.2023
- Impfdatum
- 19.06.2023
- Beginn
- 19.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Pt, 12-Year-old Female was in the office on 6/19/2023 for a Well Child visit. In the appointment notes it stated she was coming in for her "11 yr", with this information, I checked the immunization records to make sure the patient was up to date, I went through past encounters to "confirm" that she did not have an 11 year well child last year (since she was already 12 years old). While checking past encounter's the appointment note for the last well child appointment stated "10 yr well child." I then pended the routine vaccinations for 11-year-olds (Tdap, HPV and Meningitis A,C,W,Y) I then went into the room to complete the rooming process as I normally would. Toward the end of this process, I informed Mom that since the patient was here for an 11-year checkup, there were routine vaccines due, and I asked if she wanted to do the HPV vaccine. Mom agreed to do the HPV. After Dr. was done conducting his examination, the vaccine orders were signed so I prepared them, put all required information in system and entered the patient's room with them. When I entered the room, the patient stated that "getting shots scare her sometimes" and that "last year they put something on my arm to make it so the shot didn't hurt as much" I then asked her if she got her flu shot last year since I, at this point, thought she missed her 11 yr well child last year and that would have been the only routine vaccine that she should have gotten. She said "yes" and there was no further mention of her getting other vaccinations last year. I proceeded to administer the vaccinations, using the numbing spray as requested by the patient. Mom stated afterward that she forgot her vaccine card that she keeps for her record of pt's vaccinations, but she would add them to it when she got home. I then advised that the information for these would be located on her after visit summary. Patient and mom exited the office. Approximately an hour and a half later, Patient's mom called the office stating that she went to write in the vaccines given at the appointment that day and noticed that she was given these vaccines last year (Meningitis A,C,W,Y and Tdap) and wanted to make sure this was not harmful to the patient. At this time, Dr. was informed of what occurred and advised that there were no ill effects from receiving these again. I looked back in the patient?s chart to see if I missed something and at this time is where I then noticed that there was documentation of the Meningitis A,C,W,Y and Tdap vaccines given last year. When I looked at the immunization record prior to pending these vaccines, I did not realize these were documented from last year. Mom was given reassurance of Dr. advice that there are no ill effects from receiving these twice and mom verbalized no further concern. This incident was then documented in her chart. No reactions have occurred at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- Not Applicable
- Aktuelle Erkrankungen
- Not Applicable
- Vorgeschichte
- Not Applicable
- Andere Medikamente
- Not Applicable
- Allergien
- Sulfa (Sulfonamide Antibiotics)
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 05.06.2023
- Impfdatum
- 01.06.2023
- Beginn
- 01.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
20 months male baby was administered Boostrix instead of Infarix; 20 months male baby was administered Boostrix instead of Infarix; This non-serious case was reported by a other health professional via call center representative and described the occurrence of wrong vaccine administered in a 20-month-old male patient who received DTPa (Reduced antigen) (Boostrix) (batch number B32NG, expiry date 13-JUN-2025) for prophylaxis. On 01-JUN-2023, the patient received Boostrix (left thigh). On 01-JUN-2023, an unknown time after receiving Boostrix, the patient experienced wrong vaccine administered (Verbatim: 20 months male baby was administered Boostrix instead of Infarix) and inappropriate age at vaccine administration (Verbatim: 20 months male baby was administered Boostrix instead of Infarix). The outcome of the wrong vaccine administered and inappropriate age at vaccine administration were unknown. Additional Information: GSK Receipt Date: 01-JUN-2023 The reporter was the medical assistant who stated that the vaccine was administered in left thigh at the medical office. The reporter consented to follow up. On the day of reporting, a 20 months patient was administered Boostrix instead of Infarix, which led to wrong vaccine administered and inappropriate age at vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 30.05.2023
- Impfdatum
- 27.05.2023
- Beginn
- 27.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Limb mass
Peripheral swelling
Symptomtext
Pt came in on 5/30, a huge area on her arm is red, swollen and she said has a lump. I advised her to take some benadryl and watch the size of the reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- high blood pressure, cholesterol, diabetes
- Andere Medikamente
- unknown
- Allergien
- keflex
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 19.05.2023
- Impfdatum
- 05.05.2023
- Beginn
- 06.05.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Skin discolouration
Tenderness
Symptomtext
Patient came in today and mentioned that they had a black and blue mark from here Tdap vaccine that started at the deltoid and ran down to her elbow. She said that it is healing up quite a bit now and only has slight pain if she touches the spot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Skin discolouration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 18.05.2023
- Impfdatum
- 21.04.2023
- Beginn
- 21.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
received vaccine at community outreach event. Vaccine History pulled prior to event, however child had vaccination during the time between the Vaccine History being pulled and the vaccine event in the community. Received meningococcal and Tdap vaccine on 4/6/23 AND again on 4/21/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 16.05.2023
- Impfdatum
- 03.05.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Circumstance or information capable of leading to medication error
Extra dose administered
No adverse event
Vaccination error
Symptomtext
No adverse event occurred, just reporting vaccination error in giving a third Shingles dose, state Immunization System showed only his first dose so the pharmacist on duty gave an additional dose (based on the system showing only one prior dose given on 2-15-22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 10.05.2023
- Impfdatum
- 10.05.2023
- Beginn
- 10.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product preparation error
Symptomtext
Menveo reconstituted with sterile diluent instead of liquid vial that Menveo comes with. No patient c/o symptoms at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation error
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Montelukast 5mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 10.05.2023
- Impfdatum
- 09.05.2023
- Beginn
- 09.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
Pt was due for Menveo vaccine and received a Trumenba Men B vaccine in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 03.05.2023
- Impfdatum
- 24.04.2023
- Beginn
- 24.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Boostrix was not given in a complete dose; This non-serious case was reported by a other health professional via call center representative and described the occurrence of incomplete dose administered in a 21-year-old male patient who received DTPa (Reduced antigen) (Boostrix) (batch number B32NG, expiry date 13-JUN-2025) for prophylaxis. On 24-APR-2023, the patient received Boostrix. On 24-APR-2023, an unknown time after receiving Boostrix, the patient experienced incomplete dose administered (Verbatim: Boostrix was not given in a complete dose). The outcome of the incomplete dose administered was unknown. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 24-APR-2023 The reporter was medical assistant. The reporter reported that a needle cracked and Boostrix was not given in a complete dose. The vaccine administration facility was the same as primary reporter. No additional adverse event details were reported at that time. The reporter consented for safety team follow up. The vaccine was not given in a complete dose as the needle cracked, which lead to incomplete dose administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 24.04.2023
- Impfdatum
- 19.04.2023
- Beginn
- 19.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental exposure to product
Exposure via skin contact
Incorrect dose administered
Syringe issue
Symptomtext
vaccine leaked out; vaccine leaked out on patient's arm; vaccine leaked out on patient's arm; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of incomplete dose administered in a 53-year-old male patient who received DTPa (Reduced antigen) (Boostrix) (batch number B32NG, expiry date 13-JUN-2025) for prophylaxis. On 19-APR-2023, the patient received the 1st dose of Boostrix. On 19-APR-2023, an unknown time after receiving Boostrix, the patient experienced incomplete dose administered (Verbatim: vaccine leaked out), exposure via skin contact (Verbatim: vaccine leaked out on patient's arm) and inadvertent exposure to vaccine (Verbatim: vaccine leaked out on patient's arm). The outcome of the incomplete dose administered, exposure via skin contact and inadvertent exposure to vaccine were unknown. Additional Information: GSK receipt date: 19-Apr-2023 The pharmacist was wondering if they need to revaccinate the patient. The reporter consented to follow-up. The patient was recently injected with Boostrix but the vaccine leaked out on the patient's arm which led to incomplete dose administered, exposure via skin contact and inadvertent exposure to vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental exposure to product
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 05.04.2023
- Impfdatum
- 04.04.2023
- Beginn
- 05.04.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Symptomtext
Pt has bruising on her forearm, however the shot was given in the shoulder
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Contusion
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- not known
- Vorgeschichte
- asthma
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 31.03.2023
- Impfdatum
- 22.03.2023
- Beginn
- 22.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Symptomtext
immunizations were not reconciled and TDAP and MMRV were given in error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 24.03.2023
- Impfdatum
- 09.03.2023
- Beginn
- 09.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse events noted. Pt received adult dose of Hepatitis B instead of pediatric dose. She was 17 years old at date of vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -