- Staat
- NJ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 07.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Back pain
Blood test abnormal
Dizziness
Hypertension
Nervousness
Syncope
Symptomtext
, Additional Details: about 5-10mins after recieving the vaccine pt complained of back pain/dizzy,fainting. sat her down gave water. she was very nervous. no site/neck,shouolder pain but back pain of the same side. she called husband. after staying for 15 mins she felt better to leave but had gone to urgent care.called in pm to follow up around 7pm. she was better. they did blood work at uc. bp was high and blood work showed a MI from past few months. nothing new. she said she was okay now. no pain or dizzy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 04.01.2023
- Beginn
- 04.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Mobility decreased
Musculoskeletal pain
Symptomtext
The patient reports that about an hour after the shot administration there was severe musculoskeletal pain and she could not lift her arm. The patients pain has now resolved but there is still significant redness and it has traveled down the arm and stopped just before the elbow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 11.11.2022
- Impfdatum
- 02.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injected limb mobility decreased
Injection site pain
Muscular weakness
Pain
Symptomtext
Since the vaccination the patient has experienced pain in his left shoulder and reduced mobility of his arm. The patient shared he has been suffering with pain in his upper left arm and reduced mobility since the vaccination. Describes soreness with movement of left arm towards his back and when he raises it overhead (most severe reaching back). He denies pain when raising straight forward or out to the side. He reports a mild weakness related to the soreness with movement. Patient has expressed desiring imaging (MIR of shoulder) to further evaluate and treat; however, patient has not completed any imaging at the time of the report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 13.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cellulitis
Chills
Injected limb mobility decreased
Injection site erythema
Pyrexia
Vomiting
Symptomtext
Patient reported not being able to move her right arm starting overnight the night she received the vaccines. She also stated she was vomiting, had fever chills, redness at the injection site. She called an ambulance and went the emergency room where she states she was told she had cellulitis due to either the injection site being contaminated or contamination of the vaccine. She was treated with cephalexin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Macrolides & Ketolides
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 20.03.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site swelling
Pain
Symptomtext
The entire upper left arm swelled up for several days and hurt a great deal. The swelling has since subsided, but I am unable to completely lift my arm above my head without some pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- Dr. prescribed an x-ray test.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypothyroidism
- Andere Medikamente
- levothyroxine, Wellbutrin, Mirena IUD
- Allergien
- cephalosporins
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 11.10.2022
- Impfdatum
- 09.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain in extremity
Symptomtext
Administered on right arm and almost 24 hours the patient developed a large red spot with pain on the inside part of the arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None known
- Andere Medikamente
- NSAID
- Allergien
- Benadryl
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 08.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site warmth
Symptomtext
Patient stated they noticed a red and warm area below the injection site to inside of elbow. When they arrived at the pharmacy on 10/04/22, they said that morning it was warm to the touch but was no longer warm as the day went on. They did not report fever or any other systemic symptoms after receieving vaccine. Followed up with patient on 10/08/22 and they stated the reaction has cleared completely
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 22.08.2022
- Impfdatum
- 18.08.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Bandaemia
C-reactive protein increased
Cellulitis
Fatigue
Headache
Immunisation reaction
Immunodeficiency
Injection site erythema
Injection site pain
Injection site swelling
Laboratory test
Leukocytosis
Malaise
Pyrexia
Shift to the left
Ultrasound scan normal
Vomiting
Symptomtext
Received vaccines on 8/18. Beginning on the evening of 08/18, the patient began to experience unexpectedly severe pain in her L deltoid with associated swelling and erythema. She began to feel fatigued with malaise and a headache shortly after despite taking Tylenol Q6H for her symptoms. This continued until 08/19 when she became febrile to 101 F and experienced one episode of NBNB emesis follow dinner. The patient fevered again to 102 F on the day of admission which prompted her mother to seek care at a health care facility. She was started on IV clinda with rapid improvement within 24 hours. Difficult to say for certain if this was cellulitis vs vaccine reaction. Given her immunocompromised status we decided to be more cautious and treat as a true cellulitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- 2,0
- Labordaten
- Leukocytosis with left shift and bandemia, fever, elevated CRP and PCT. US showed no fluid collection.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Evans syndrome ( ITP and hemolytic anemia d/t warm antibodies)
- Andere Medikamente
- Sirolimus, erythromycin, Nexplanon, desonide ointment for lips
- Allergien
- Amoxicillin/penicillin
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 04.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Injection site swelling
Monoplegia
Symptomtext
PATIENT REPORTED A SWOLLEN ARM AND INJECTION SITE. PATIENT STATED THE ARM WAS PARALYZED AND PAINFUL FOR A SHORT TIME
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 05.07.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site swelling
Symptomtext
Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chills
Fibrin D dimer increased
Headache
Pain in extremity
Peripheral swelling
Ultrasound Doppler normal
Symptomtext
Headaches, chills, left arm pain and swelling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Positive D-dimer on 6/05/22 Ultrasound of left upper extremity was negative for DVT on 6/05/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, hyperlipidemia, hypothyroidism, prediabetes, asthma, GERD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 21.05.2022
- Impfdatum
- 18.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site warmth
Symptomtext
Patient stated that the site of his pneumovax shot is red and warm. Started a couple of days after shot He stated he is sensitive to shots. Will keep an eye on it and use a cold pak.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 19.05.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Dysstasia
Gait disturbance
Symptomtext
ACUTE STABBING LOWER BACK PAIN NEAR WASTE. PATIENT ATTEMPTED TO WALK OUT OF LOBBY SEVERAL MINUTES AFTER RECEIVING VACCINE, CALLED FOR HELP AND COULDN'T STAND. SHE SAT DOWN IN A CHAIR AND ASKED ME TO CALL EMERGENCY SERVICES, WHICH I DID. AFTER PARAMEDICS CHECKED HER OUT, SHE DECLINED TRANSPORT TO ED AND WALKED OUT OF STORE ON HER OWN POWER. SHE SAID THE PAIN WAS NO LONGER THERE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- PATIENT REPORTED HISTORY OR SCIATICA AND FALL ONE MONTH EARLIER
- Andere Medikamente
- FLUOXETINE 10 MG TWICE DAILY LEVOTHYROXINE 100 MCG ONCE DAILY ALENDRONATE 70 MG ONCE WEEKLY CARVEDILOL 6.25 MG ONCE DAILY IN THE MORNING AND TWO TABLETS AT NIGHT
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 14.05.2022
- Impfdatum
- 09.05.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Pain
Swelling
Tenderness
Symptomtext
Tenderness in the arm, swollen and pain. patient went to emergency room.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 08.05.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Additional Details: gave pt zyrtec 10mg to take at home, and advised trial of ibuprofen. pt will try and if no relief, will report to her dr
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site pain
Vaccination site rash
Vaccination site swelling
Symptomtext
Patient said suffered soreness, rash and swelling at the vaccination site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- Famotadine 20mg; meclizine 25mg
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 14.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site swelling
Symptomtext
Patient developed pain,swelling over injection site that progressed to involving the upper arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma,Allergic Rhinitis
- Andere Medikamente
- Singulair 10mg daily,Zyrtec 10mg daily,Albuterol HFA 2 puffs 4 times daily as needed.
- Allergien
- Seafood,Penicillin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 03.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain in extremity
Peripheral swelling
Symptomtext
Patient's arm really swollen and red plus pain. Her doctor gave her a prednisone 5mg 6 days pack to help with the reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood Pressure
- Andere Medikamente
- amlodipine, lisinopril, hydrochlorothiazide, atorvastatin
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pain
Injection site pruritus
Symptomtext
Patient's Arm beneath the injection site was red, sore, tender to touch, painful but could still be moved. Pain and redness lasted for 3-4 days post vaccination. Pain started the same day, several hours post vaccination. Pictures were documented and sent to MD office. Treated pain with celecoxib x 2. Patient reported a little itchy on day 6 and still a little red.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- No medical test or laboratory test were done for this adverse event. HOWEVER, pharmacist wanted to submit this ALONG WITH COVID VACCINATION INFORMATION because this adverse event has occurred to this patient and anecdotally reported to me by 2 other patients who have received PPSV23 post COVID vaccinations, more so now post COVID vaccinations then ever before. This particular patient received Pfizer COVID vaccines on 2/17/21, 03/10/2021, and 12/19/2021. The other 2 patients were not my patients but they told me their story. Should we doing a little more patient warning to patients who have been receiving the PPSV23 post COVID ?
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Erythema
Pain in extremity
Peripheral swelling
Skin warm
Symptomtext
Extreme swelling and pain first evening in upper arm progressing into bicep overnight. Second day becoming hot and red. Second night into morning, swelling and redness into elbow area. Had pre-scheduled appointment with oncologist on morning of 2/11/22. Diagnosed as cellulitis and prescribed Cephalexin 500 mg capsule 1-4x a day. Went to pick up prescription at same pharmacy where vaccine was administered and was told to report on CDC website.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- CLL
- Vorgeschichte
- -
- Andere Medikamente
- diltiazem, finasteride, hydroxycholorquine, aspirin, multi vitamin, fish oil
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Decreased appetite
Headache
Lymphadenopathy
Malaise
Pain
Peripheral swelling
Pyrexia
Symptomtext
Approximately 16 hours after vaccine administration developed 101 degree fever, severe body aches, chills, severe headache, swelling in right arm and in right auxiliary lymph notes, mailaise, loss of appetite
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Covid 19 positive on 06 Jan 2022
- Vorgeschichte
- N/A
- Andere Medikamente
- Brevicon
- Allergien
- Clindamycin, ceclor, sulfa drugs, azithromycin
- Vorherige Impfungen
- Moderna COVID-19 vaccine second and third booster in Feb 2021 and Nov 2021, developed headache, fever, malaise, chills, body ach
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 31.10.2023
- Impfdatum
- 25.10.2023
- Beginn
- 25.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No additional AE/PQC.; HCP calling to report AE for expired dose of PNEUMOVAX 23 PFS that was administered to a patient on 25OCT2023. Product expired 29JAN2023. Product did not have any previous temperature excursions. No side effects were reported. No other medical inform; This spontaneous report as received from a physician refers to a patient of unknown age and gender. No information regarding the patient's concurrent conditions, medical history and concomitant medications was provided. On 25-OCT-2023, the patient was vaccinated with an expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) lot # U022984, expiration date 29-JAN-2023 (dose, route of administration and anatomical location were not reported) for prophylaxis (Expired product administered). The suspect vaccine did not undergo temperature excursion. No side effects were reported (No adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- -
- Geschlecht
- U
- Eingang
- 25.07.2023
- Impfdatum
- 22.06.2023
- Beginn
- 22.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patients involved have not experienced any symptoms related to this adverse event at this time / No additional AE; Pharmacist calling to report adverse event regarding expired doses of PNEUMOVAX 23 that were inadvertently administered on 6/22/2023; This spontaneous report was received from a pharmacist, concerning a patient of unknown age and gender. The patient's medical history, concurrent conditions, historical drugs, and concomitant therapies were not reported. On 22-JUN-2023, the patient was inadvertently vaccinated with an expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, 0.5 ml, once (lot number U022984 was verified to be valid, expiration date reported and confirmed as 29-JAN-2023) (route of administration and anatomical location were not provided) (Expired product administered). The patient did not experienced any symptoms related to this adverse event at this time. This is one of two reports received from the same reporter. ; Sender's Comments: US-009507513-2307USA011007:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.05.2023
- Impfdatum
- 24.05.2023
- Beginn
- 24.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Pharmacist reported that an expired PNEUMOVAX 23 was administered to a patient. No additional AEs were reported. No further information provided. No PQC.; This spontaneous report has been received form a pharmacist, regarding a patient of unknown age and gender. The patient's pertinent medical history, previous drug reactions or allergies and concomitant medications were not reported. On 24-MAY-2023, the patient was vaccinated with an expired Pneumococcal Vaccine, Polyvalent (23-valent) (PENUMOVAX23) injection, as prophylaxis (lot number: U022984, which was determined to be valid as syringe, with an expiration date on 29-JAN-2023) (strength, dose, scheme, route and anatomical location of administration were not reported). No additional adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 24.03.2023
- Impfdatum
- 26.02.2023
- Beginn
- 26.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No additional AE reported; expired PNEUMOVAX 23 that was administered yesterday 2/26/2023.; This spontaneous report was received from a pharmacist and referred to a patient of unspecified age or gender. The patient's medical history, concurrent conditions, concomitant therapies and drug reaction/allergies were not reported. On 26-FEB-2023, the patient was vaccinated with expired pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, 0.5 milliliter, lot #U022984, expiration date: 29-JAN-2023, administered for prophylaxis (strength and route of administration were not provided) (Expired product administered). No additional adverse event details available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- M
- Eingang
- 08.03.2023
- Impfdatum
- 03.03.2023
- Beginn
- 03.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; expired lot of PNEUMOVAX 23 was administered to 69 year old patient; This spontaneous report was received from a pharmacist and refers to a 69-year-old male patient. No information regarding patient's medical history, drug reactions or allergies and concomitant therapies was provided. On 03-MAR-2023, the patient was vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) lot # U022984, expiration date: 29-JAN-2023, 0.5 milliliter once (route of administration and anatomical location were not reported) for prophylaxis (expired vaccine used). No further information and no additional adverse event were provided (No adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 03.03.2023
- Impfdatum
- 03.03.2023
- Beginn
- 03.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
I GAVE AN EXPIRED DOSE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- ALSO REC'D SHINGRIX #1 AND BOOSTRIX AT THE SAME TIME
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- -
- Geschlecht
- U
- Eingang
- 01.03.2023
- Impfdatum
- 31.01.2023
- Beginn
- 31.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No additional AE reported; expired PNEUMOVAX 23; This spontaneous report was received from a nurse referring to a patient of unknown age and gender. The patient's medical history, concurrent conditions, concomitant medications and drug reaction/allergies were not reported. On 31-JAN-2023, the patient started therapy with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, lot #U022984, expiration date: 29-JAN-2023 (strength, dose, anatomical site of administration and route of administration were not provided) administered for prophylaxis (expired product administered). No additional adverse event (AE) reported (no adverse event). No temperature excursion reported for affected pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) prior to or at current call time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- -
- Geschlecht
- U
- Eingang
- 20.02.2023
- Impfdatum
- 15.02.2023
- Beginn
- 15.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient was administered and expired PNEUMOVAX 23.; This spontaneous report has been received from a nurse referring to a patient of unknown age and gender. The patient's pertinent medical history, drug reactions, allergies and concomitant medications were not reported. On 15-FEB-2023, the patient was vaccinated with an expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, lot number U022984 with expiration date 29-JAN-2023, administered for prophylaxis (strength, specific dosage, vaccination scheme, route of administration and anatomical site of application were not provided) (expired product administered) No other issues or concerns noted. No product quality complaint or temperature excursion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- -
- Geschlecht
- U
- Eingang
- 18.07.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.06.2022
- Tage bis Beginn
- 182,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
no adverse reaction or symptoms; a dose of PNEUMOVAX 23 was ordered to be given in December 2022. However, the dose was given today, 06/30/2022; This spontaneous report was received from a medical assistant referring to a patient of unknown age and gender. Information about pertinent medical history, drug reaction/allergy and concomitant medication was not provided. On 30-DEC-2021, the patient was vaccinated with pneumococcal vaccine conj 13v (crm197) (PREVNAR 13) (strength, dose, route of administration, anatomical location, indication, lot# and expiration date were not reported). On 30-JUN-2022, the patient was vaccinated with an early dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) (lot # U022984, expiration date was not reported, but upon internal validation established as 29-JAN-2023; strength, dose, route of administration and anatomical location were not reported) for prophylaxis, which was ordered to be given in December 2022 (inappropriate schedule of product administration). The patient had no adverse reaction or symptoms from receiving either vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 18.02.2022
- Beginn
- 20.03.2022
- Tage bis Beginn
- 30,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Duodenal ulcer
Gastrooesophageal reflux disease
Iron deficiency anaemia
Oesophagogastroduodenoscopy abnormal
Vascular cauterisation
Symptomtext
Iron deficiency anemia due to chronic blood loss - He was given 80 mg IV protonix, Zofran, 2 g IV magnesium in ED. On admission, GI was consulted. Underwent EGD on 3/21 which showed reflux esophagitis, and a deeply cratered non-bleeding duodenal ulcer with visible vessel. Vessel treated with bipolar cautery. Discharged home. ED visit to hospital admission within 6 weeks of receiving hte COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Duodenal ulcer
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Peripheral swelling
Symptomtext
ABNORMAL SWELLING OF THE UPPER ARM AND LYMPH NODES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -