- Staat
- PA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 06.10.2021
- Beginn
- 10.10.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain upper
Laboratory test
Loss of consciousness
Symptomtext
vaccines received 10/6 - on 10/10 patient passed out and was taken to ER with stomach pains. tests were run and no cause was able to be determined
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 22.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amnesia
Injected limb mobility decreased
Vaccination site pain
Vaccination site swelling
Injection site pain
Injection site swelling
Muscular weakness
Pain in extremity
Peripheral swelling
Symptomtext
The arm she received the vaccine in started to swell adn she felt pain; The arm she received the vaccine in started to swell adn she felt pain; Suffers from short term memory loss; "When I go to raise my arm I have to use my other arm to lift it up"; This spontaneous report has been received from a consumer referring to herself, a 83-year-old female patient. The patient's pertinent medical history included hypothyroidism. Concomitant therapies included: metformin, losartan, euthyrox, glipizide, clopidogrel, atorvastatin, metoprolol, baby aspirin, and benzonatate. The patient's previous drug reactions or allergies were not provided. On 22-MAR-2022, the patient was vaccinated with an unspecified pneumoccocal injection vaccine administered as prophylaxis (dose, route of administration, vaccination scheme frequency, anatomical location, lot number and expiration date were not provided). On 23-MAR-2022, the patient experienced swell and pain in the arm where she received the vaccine (vaccination site swelling) (vaccination site pain). On an unknown date in 2022, when the patient went to raise her arm she had to use her other arm to lift something up (injected limb mobility decreased); additionally, she experienced short term memory loss (amnesia). At the time of reporting, she had not recovered from any of the events. The causal relationship between the events and the unspecified pneumococcal vaccine was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hypothyroidism
- Vorgeschichte
- -
- Andere Medikamente
- METFORMIN; LOSARTAN; EUTHYROX; GLIPIZIDE; CLOPIDOGREL; ATORVASTATIN; METOPROLOL; BABY ASPIRIN; BENZONATATE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood culture negative
Blood lactic acid
Culture urine positive
Full blood count
Lactic acidosis
Leukocytosis
Metabolic function test normal
Pain in extremity
Peripheral swelling
Pyrexia
Tachycardia
Tachypnoea
Ultrasound Doppler normal
White blood cell count increased
Symptomtext
Admission to hospital for fever, tachypnea, tachycardia, leukocytosis, and lactic acidemia. Pain and swelling of left arm. Patient was admitted to the hospital for IV antibiotics, hydration, and supportive care. LUE duplex was negative. Discharged after 3 days as in patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- 3,0
- Labordaten
- 11/12 CBC with WBC = 22.3, Lactic Acid = 1.5, Blood Culture = Negative, Basic Metabolic Profile= WNL, Urine Culture= probable contaminant.
- Aktuelle Erkrankungen
- Crohn's Flare
- Vorgeschichte
- Crohn's Disease, Depression, IBD,
- Andere Medikamente
- Xanax, Fioricet, Masalamine, Micronor, Zofran, Senna-docusate,
- Allergien
- Kiwi, Adhesive Tape, Vancomycin, Benzoyl Peroxide
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 07.10.2021
- Impfdatum
- 04.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Injection site rash
Injection site swelling
Injection site warmth
Pain
Pain in extremity
Symptomtext
Patient received 3 vaccines on 10/4/21. Received Shingrix in right arm and both Pneumovax 23 and Flublok in left arm. (PPSV23 lower and to right, Flublock upper and to left from ppsv23 separated by at least 1 inch.) Patient called today 10/7/21 stating the following reaction in left arm. Patient had pain in arm which has been improving. Very sore where patient really unable to use at beginning. She says pain has been an ache but now more of a throb. She checked arm yesterday and noticed a rash. Says rash is spreading, larger area today. covers top half circumference of her arm, (180 degree circumference.) Width is about 3 inches (top to bottom). She says the area is warm to the touch. No itching. When I asked her if the area was swollen she said she thinks so. She has been taking tylenol and ibuprofen which she says has not been helping much, She has been icing the area and says she was putting hydrocortisone cream on the area. Patient states no fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 11.09.2022
- Impfdatum
- 30.08.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site cellulitis
Symptomtext
Cellulitis at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site cellulitis
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- Brilinta 90 mg, metoprolol er 25 mg
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 19.12.2021
- Impfdatum
- 26.08.2021
- Beginn
- 31.08.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypersensitivity
Injection site discomfort
Injection site erythema
Injection site pain
Injection site warmth
Symptomtext
Narrative: pt presents for triage, c/o allergic reaction to TDAP given 8/26/21 pt rt upper arm, red below deltoid and above elbow...warm to touch. pt states didn't noticed till yesterday. took 2 benedryl tabs last night. states sore and burning sensation . Right upper arm with 3in X 3in area warm, red. No swelling. Feels like a sunburn. No blisters. Area appears to be allergic reaction and he di dhave some imprvement with burning discomfort after benadryl 50mg last night. VSS w/ no SOB, facial or throat edema, or wheezing. Afebrile
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discomfort
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- Impfdatum
- 11.10.2021
- Beginn
- 11.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Pyrexia
Respiration abnormal
Symptomtext
Pt stated that he started with a HA about 2 hours after receiving the vaccine and then had a fever of 101.8 for 1 day. HA continued on the second day with some abnormal breathing. Patient reported after all symptoms were resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Pt had dental appt on 10-7-2021 and was prescribed amoxicillin 2g to take 1 hour prior to procedure
- Vorgeschichte
- Diabetes Hypertension hyperlipidemia obesity
- Andere Medikamente
- unknown
- Allergien
- meloxicam tomatoe nickel
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 21.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Swelling
Symptomtext
great deal of itching, kept moving as far as locality, raised itchy sights, intense, went away after a few days, pt had also gotten 2nd shingrix shot and fluzone hd, on that same day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 98,0
- Geschlecht
- F
- Eingang
- 15.10.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site oedema
Injection site pain
Injection site swelling
Symptomtext
Pt had severe pain and swelling at injection site, fluid build up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site oedema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HTN, OSA, hyperthyroidism, hyperlipidemia, osteoarthritis
- Andere Medikamente
- Dulcolax 5mg, Miralax, Ocuvite, Ondanestron, Senns-S, Zyrtec, Aleve, Voltaren gel, Omeprazole, Metoprolol, Levothyroxine, Amlodipine, hydrocodone bitartrate/acetaminophen,
- Allergien
- Lansoprazole
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 13.10.2021
- Beginn
- 13.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Dizziness
Flushing
Hyperhidrosis
Malaise
Pain
Symptomtext
patient recieved both vaccines and stood to leave. about two minutes later patient returned to pharmacy and reported "not feeling well". Pharmacist guided patient to a chair to sit down. Once seated, reported feeling dizzy upon being asked what she was experiencing. Shortly after, patient reported severe back pain, began to become flush, and started to perspire. Patient was asked if she wanted to emergency services to check her out to which she agreed. While waiting for their arrival, pharmacist inquired is patient was having any difficultly breathing or if there was any pain originating for injection site which patient denied. Patient was instructed to take slow, deep breaths to help her remain calm. After a few minutes, patient reported that pain was subsiding. Once EMT's had arrived and patient was assessed she was given the option to be transported for further care, which she declined. After patient had spent a few more minutes seated, she decided to leave. She was again asked if she was feeling well and was invited to remain if she needed to more time to recover. Patient declined to remain seated and departed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- uNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- XARELTO 20MG, fLUOXETINE 20MG,
- Allergien
- CODEINE
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 10.10.2021
- Beginn
- 11.10.2021
- 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 reaction
Injection site swelling
Injection site urticaria
Urticaria
Symptomtext
Pt stated she was experiencing swelling at the injection site and had welts/hives around the injection site as well, starting approximately the day after injection. Pt has been using ice pack, benadryl, and ibuprofen to help with symptomatic relief, but symptoms still have not resolved and will be going
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 06.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Erythema
Mass
Pyrexia
Skin warm
Urticaria
Symptomtext
Patient called on 10/13/2021 and stated during the evening on 10/6/2021 hives appeared on left shoulder to arm, fever, chills, and a red lump that was warm to the touch. Symptoms resolved within 48 hours. Patient did not seek medical attention. Patient did not take any medication to relieve symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Bactrim
- Allergien
- Bee
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 05.10.2021
- Impfdatum
- 04.10.2021
- Beginn
- 04.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Erythema
Pyrexia
Symptomtext
The patient developed cellulitis. Warm, redness and fever that radiated down her arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Pain in extremity
Wrong product administered
Symptomtext
Pharmacist is submitted VAERS report about a vaccine administration error. Patient was indicated for Prevnar13, but due to pharmacist dispensing error, patient was given Pneumovax23 instead. It is believed that patient received Pneumovax23 in 2018, so she was not indicated for Pneumovax23 until 2023. Patient experienced a sore arm after the vaccine. Patient did not report any additional side effects to the vaccine. Patient is concerned about the vaccine schedule for the pneumonia shot, since she received a second Pneumovax23 vaccine before the 5 year gap that is recommended in vaccine guidelines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Autoimmune disorder, arthritis,hypothyroidism
- Andere Medikamente
- Methotrexate
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 29.09.2021
- Impfdatum
- 21.09.2021
- Beginn
- 21.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Vaccination site erythema
Vaccination site rash
Vaccination site warmth
Symptomtext
WARM, RED, NON-ITCHY RASH ON VACCINATION ARM (FLUZONE AND PNEUMOVAX 23), ER VISIT, PT RECIEVED STEROIDS AND ABX
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO KNOWN ILLNESSES
- Vorgeschichte
- NO KNOWN HEALTH CONDITIONS
- Andere Medikamente
- UNKNOWN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 22.09.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 5,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain in extremity
Peripheral swelling
Symptomtext
Patient reported to pharmacy experiencing pain, redness and swelling on the arm that she received the vaccinations. Reported to pharmacy 5 days after vaccine with unknown onset time. Patient reported going into clinic to be seen stating she was told to take benadryl and put an unknown cream on arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 05.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Symptomtext
redness, swelling, itching at site of vaccine. on 9/5 redness has gotten larger than before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- allergic to adhesives, rash
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.12.2022
- Impfdatum
- -
- Beginn
- 03.11.2022
- Tage bis Beginn
- -
- 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; dose of PNEUMOVAX 23 expired on 9/13/2022 and was administered on 11/3/2022; This spontaneous report has been received from a pharmacist concerning a patient of unreported age and gender. The patient's medical's history, drug reactions or allergies, concurrent conditions and concomitant medications were not reported. On 03-NOV-2022, the patient was vaccinated with a dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) 0.5 ml, lot # U002528, expiration date 13-SEP-2022 (route of administration and anatomical location were not provided) as prophylaxis (expired product administered). It was reported that no temperature excursions occurred previously. No additional events 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
- FL
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- 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's and no PQC's were reported.; A nurse reported that an expired dose of PNEUMOVAX 23 was administered to a patient.; This spontaneous report was received from a registered nurse concerning a patient of unknown gender and age. The patient's concomitant therapies, pertinent medical history, and drug reactions/allergies were not reported. On 06-OCT-2022, an expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) (lot # U002528, expiration date 13-SEP-2022; strength, dose, route of administration were not reported) was administered to the patient (expired product administered). No additional adverse events (AEs) were reported.
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
- 05.10.2022
- Impfdatum
- 23.09.2022
- Beginn
- 23.09.2022
- 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; product expired on 9/13/2022 and was administered; This spontaneous report was received from a licensed practical nurse and refers to a patient of unknown age and gender. The patient's pertinent medical history, current conditions, drug reactions or allergies and concomitant medications were not reported. On 23-SEP-2022, the patient was vaccinated with an expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, lot #U002528, expiration date: 13-SEP-2022, administered for prophylaxis (dose, strength, site, and route of administration were not provided) (expired product administered). Customer confirms the product was stored appropriately and did not have any temperature excursions prior to administration. No additional adverse events details or product quality complaints 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
- IL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 23.09.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient was given an expired dose of the vaccine. The vaccine expired on 9/13/22 and was given on 9/23/22 Patient condition was the same after the injection as it was before injection Physician was notified and she did not want vaccine repeated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- non
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension history of CVA Thyroid nodule
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 25.08.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Symptomtext
Swelling of arm that the patient received injection on. Started the same day as injection but seemed to be better the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Peripheral swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 17.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Peripheral swelling
Symptomtext
Swelling on the back of the arm (triceps) down to elbow
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Peripheral swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Iodine, Aspirin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypersensitivity
Hypophagia
Mouth swelling
Oral discomfort
Symptomtext
Patient called on 04/12/22. She said she had a terrible time this last few weeks because she had an allergic reaction to the vaccine in her mouth. She said she had some swelling inside her mouth and she couldn't eat. She said her mouth was burning, around her lips, mouth. She said she is getting better now. She just wanted us to let us know.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypersensitivity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 20.11.2021
- Impfdatum
- 20.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Product dispensing error
Symptomtext
Patient pulled arm away when administering vaccine. Had to re-stick patient to administer vaccine. Whole dose administered with 2nd needle stick to arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 65,0
- Geschlecht
- U
- Eingang
- 27.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
no adverse event; patient was accidently was given both PNEUMOVAX23 and PREVNAR 13 on the same day; This spontaneous report was received from a registered nurse referring to a 65-year-old patient of unknown gender. The patient's pertinent medical history, concurrent conditions, drug reactions/allergies and concomitant medications were not provided. On 12-OCT-2021, the patient was accidently vaccinated with pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) 0.5 ml, lot # U002528, expiration date on 13-SEP-2022, for prophylaxis (strength, route of administration and anatomical location were not reported) and pneumococcal vaccine conj 13v (crm197) (PREVNAR 13) 0.5 ml, lot #CK0842, expiration date on 01-FEB-2022 on the same day (accidental overdose). At the time of report, the patient had not experienced any additional adverse event (no adverse event). Vaccines were administered together and there was no guidance on the administration of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) with pneumococcal vaccine conj 13v (crm197) (PREVNAR 13) in the prescribing information for pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 05.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 02.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Monoplegia
Peripheral swelling
Symptomtext
Patient stated that her arm was very sore and swollen - she called the pharmacy and informed us of this approximately 4 days after the vaccines were administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Monoplegia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Acyclovir 200mg Metoprolol 50mg ER Alendronate 70mg KCl 10 MEQ Furosemide 20mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 17.09.2021
- Beginn
- 18.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Erythema
Infection
Swelling
Symptomtext
Redness, swelling, systemic infection. Pt was seen in the hospital, treatment unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Not known
- Vorgeschichte
- Not known
- Andere Medikamente
- Prazosin, Duloxetine, Clonazepam, Aripiprazole, Tradjenta. List may be incomplete.
- Allergien
- No known allergies
- Vorherige Impfungen
- -