- Staat
- SC
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 06.02.2023
- Impfdatum
- 01.02.2023
- Beginn
- 03.02.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- ID / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Sudden death
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sudden death
- Hospital-Tage
- -
- Labordaten
- Unknown. Body in the care of Coroner's Office. Autopsy pending to the best of my knowledge.
- Aktuelle Erkrankungen
- HIV positive History of syphilis-Treated Anxiety Methamphetamine abuse Tobacco abuse
- Vorgeschichte
- HIV positive Methamphetamine abuse IV drug use Tobacco abuse Anxiety
- Andere Medikamente
- Biktarvy
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 19.08.2022
- Impfdatum
- 14.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Acute myocardial infarction
Chest discomfort
Electrocardiogram normal
Jaw disorder
Muscle tightness
Troponin increased
Symptomtext
Patient presented to ED on 8/17/22 with NSTEMI after receiving one dose of Jynneos vaccine (administered on 8/14/22). The symptoms included chest tightness/heaviness which radiated to his jaw, lasted for about three hours, and resolved prior to ER admission.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 3,0
- Labordaten
- Initial troponin 4.17 Trending troponin: 13.15 -- > 9.72 -- > 5.18 -- > 5.09 -- > 6.23 EKG with no acute ST changes
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HIV
- Andere Medikamente
- Genvoya
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 11.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Presyncope
Syncope
Symptomtext
Upon post vaccination for second dose of monkeypox, patient had a vasovagal episode with syncope. Patient brought safely to floor with legs elevated and ice packs applied. Water offered. Vital signs taken and patient expressed resolution of symptoms 10 seconds post syncope. Patient vitals within normal limits. Patient contacted friend to accompany out of the facility. Patient left facility safely.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 08.10.2022
- Impfdatum
- 08.10.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Loss of consciousness
Syncope
Symptomtext
After receiving vaccination, 2 minutes later, patient fainted at 1123. Nurse elevated patient's legs, cold compress applied to back of neck. Patient regained consciousness within the next minute. Patient denied feeling dizziness and lightheadedness. First set of vital signs initiated. BP, RR, pulse ox all WNL. HR was 50, but patient reported that is her baseline as she states she "runs and exercises often". Second and third set of vital signs initiated and both WNL. Patient reported feeling better and brought to observation at 1140 where patient stayed an extra 15 minutes. Patient left in stable condition at 1155.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Hyperhidrosis
Pallor
Syncope
Symptomtext
Patient received 1st dose of Mpox Jynneos vaccine ID. At 5:09 pm after receiving vaccine, patient complained of lightheadedness, became pale and diaphoretic. The patient fainted for 3 seconds. Immediately elevated the legs, applied cold packs, offered water and placed patient on the floor. Initiated vital signs. Observation extended to 30 minutes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 01.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
Pt was screened to receive the 1st dose of the Jynneos/BN vaccine. No contraindications to vaccination. After intradermal administration, pt briefly passed out in the chair before regaining consciousness. Pt was guided to the floor by this RN and RN managers. Oxygen saturation 98%. Pulse 89 bpm. Blood pressure readings were as follows: 100/60 laying down, 110/66 laying down, 112/80 sitting in chair. Pt recovered and was guided to the post vaccination area for additional observation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 30.09.2022
- Impfdatum
- 26.09.2022
- Beginn
- 27.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Facial paralysis
Symptomtext
Given second Monkeypox vaccine 9/26/22, experienced facial paralysis 9/27/22. Went to urgent care, no PCP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- syphilis
- Vorgeschichte
- HIV/AIDS
- Andere Medikamente
- Biktarvy Ritalin Doxycycline Hyclate
- Allergien
- Naproxyn
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 28.09.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Loss of consciousness
Pallor
Symptomtext
pt was noted pale ad diaphoretic and sudden loss of consciousness. Placed on flat surface and legs elevated. Regained consciousness after 10 seconds. Vital signs initiated, cold pack provided, offer water. No other complains presented. Closely monitored for 30 mins. Symptoms resolved left at 12:20 in stable conditions. Health education provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 28.09.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
After few seconds of getting the vaccine, client loss consciousness on his way to observation and was held by staff. Assisted to sit on chair. No injuries noted. Client's legs elevated. Vital signs were taken. Client regained consciousness after 10 seconds and stated he is feeling better. Client stated he didnt eat breakfast before getting the vaccine. Water offered, tolerated well. Client was observed for 30 minutes. At 10:40 am, client AOX4, left the site on stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 25.09.2022
- Impfdatum
- 25.09.2022
- Beginn
- 25.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Symptomtext
Post vaccination client complains of feeling light headed and loss consciousness for 3secs. Vital signs initiated taken 3X, legs elevated , icepacks provided, observation time extended. After 20 mins. client stated she was feeling better and advised she hasn't had anything to eat or drink since in the morning. Client left the facility ambulating with no signs of distress at 6:30pm. Client educated to call EMS if symptoms persists. Client confirmed understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 24.09.2022
- Impfdatum
- 24.09.2022
- Beginn
- 24.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Immediate post-injection reaction
Syncope
Symptomtext
Immediately after receiving vaccine patient was diaphoretic and experienced syncopal episode. Regained consciousness after 10 seconds. symptoms resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- 3:31 HR 79 R 16 BP 110/70 sat 98%
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 22.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient received 2nd dose of Jynneos vaccine on the left forearm. Patient had a syncopal episode upon seeing the bleb at the site of vaccination. The episode lasted for about 10 seconds. Observation time was extended an additional 15 minutes and 3 sets of vital signs were taken all within normal limits. Bilateral lower extremities were elevated, ice packs were applied and water was provided. Patient expressed relief of symptoms and left the facility safely once the observation period finished.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 22.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient received second dose of Monkeypox vaccine at 1130. Patient vaccinated intradermally, sitting down. Post vaccination, patient experienced a syncopal episode which resolved after 10 seconds. Bilateral lower extremities elevated, ice packs applied, water provided. Patient safety maintained. 4 sets of vitals taken, all within normal patient?s baseline. Patient observation time extended an additional 15 minutes. Post observation period, patient stated complete resolution of symptoms and left facility safely with their partner.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 22.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient received second dose of Monkeypox vaccine at 1000. Patient vaccinated intradermally, sitting down. Post vaccination, patient experienced a syncopal episode which resolved after 5 seconds. Bilateral lower extremities elevated, ice packs applied, water and protein bar provided as patient stated they did not eat breakfast. Patient safety maintained. 3 sets of vitals taken, all within normal baseline. Patient observation time extended an additional 15 minutes. Post observation period, patient stated complete resolution of symptoms and left facility safely.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 22.09.2022
- Impfdatum
- 21.09.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Hyperhidrosis
Syncope
Symptomtext
Patient experienced a syncopal episode after receiving dose. He fell as he was walking to the observation area . The episode was witnessed . Patient became diaphoretic. Recovered uneventfully EMS were on scene . Patient did not require transport to ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Vital signs
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 20.09.2022
- Impfdatum
- 20.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Dyskinesia
Loss of consciousness
Pallor
Symptomtext
Patient complaint of lightheaded. Patient passed out after receiving the vaccine. Patient jerked for 2 seconds. Patient was pale. Client regained consciousness after 4-5 seconds . Lowered on the ground, legs elevated. vitals checked, ice pack applied., and water provided. Patient color regained . 45 observation. Patient left the site with steady gait with his partner
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 20.09.2022
- Impfdatum
- 20.09.2022
- Beginn
- 20.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Pt had syncopal episode for 1-3 seconds. Able to regains to self after. Pt claims had previous event every time having injection done. No other medical conditions claimed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Nka
- Vorherige Impfungen
- Lightheadedness after Im injections
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 20.09.2022
- Impfdatum
- 20.09.2022
- Beginn
- 20.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Feeling cold
Hyperhidrosis
Syncope
Symptomtext
Patient had an episode of fainting for about 30 seconds after receiving intradermal jynneos vaccination for Monkeypox. After pt recovered from fainting, he was alert and oriented x3. He complained of feeling cold, clammy and diaphoretic. Pt was later flat, vitals initiated and offered water. Pt observation was extended for 30 minutes. Pt stated he felt much better after observation ended. Pt was able to walk with a steady gait, denied any of the earlier symptoms mentioned. Left in stable condition via ambulatory. Encouraged to seek medical attention for any adverse reactions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Plantar fasciitis
- Andere Medikamente
- Multivitamin
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 19.09.2022
- Impfdatum
- 19.09.2022
- Beginn
- 19.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyporesponsive to stimuli
Immediate post-injection reaction
Loss of consciousness
Symptomtext
Immediately post vaccination at 1753, pt appeared slightly less responsive than normal. Legs elevated, ice packs applied to nape of neck. Water provided to the pt. The pt lost consciousness for approximately 10 seconds. VS initiated, WNL. Pt denied hx of vasovagal. VS taken q4. At 1808, pt verbalized that he was feeling better. Pt was escorted over to observation for an additional 15 minutes. Pt left observation at 1824, ambulatory with a steady gait. Pt left alone in an uber with all symptoms resolved. Education provided to pt regarding when to seek medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Mild rashes from penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 19.09.2022
- Impfdatum
- 12.09.2022
- Beginn
- 19.09.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Bradycardia
Immediate post-injection reaction
Loss of consciousness
Pallor
Posture abnormal
Symptomtext
Pt reported hx of vasovagal to vax RN. Pt was advised that due to medical hx, it would be preferred to vaccinate the pt lying down, however the pt refused. Immediately post injection at 1026, the pt appeared pale and began to lull/sag forward. Legs were elevated. Pt was stabilized by additional RN. Ice packs were applied to nape of neck and chest. Pt lost consciousness for approximately 15 seconds. Pt began to arouse while still sitting in the chair but was quickly transferred over to the cot where VS were initiated. VS q3 WNL aside from slight bradycardia with set one and four, later determined to be pt baseline. At approximately 1036, pt reported feeling better. Pt was transferred to a seated position at approximately 1041, tolerated well. Pt moved to stand at approximately 1045, tolerated well. Pt then walked over to observation at 1046 for an additional 20 minutes after reporting feeling completely better. Pt left observation with roommate at 1106 ambulatory with a steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HX of vasovagal
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 18.09.2022
- Impfdatum
- 18.09.2022
- Beginn
- 18.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Heart rate decreased
Hyperhidrosis
Loss of consciousness
Pallor
Symptomtext
Approximately two minutes post vaccination, patient appeared pale, clammy, and diaphoretic. Patient then lost consciousness for a few seconds. Legs were immediately elevated. Ice packs applied to nape of neck. Patient regained consciousness on his own with no intervention. Water provided to patient. VS initiated Q3. HR slightly low but non significant with set one. A&O x3. After approximately 10 minutes, patient reported feeling completely better with no symptoms. Patient escorted over to observation for an additional 15 minutes. Patient left observation on his own ambulatory, with steady gait, reportedly feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 18.09.2022
- Impfdatum
- 18.09.2022
- Beginn
- 18.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adverse event
Dizziness
Loss of consciousness
Syncope
Symptomtext
Syncopal Episode: lightheadedness, dizziness After about 7 seconds the patient regained consciousness. Feet was elevated and ice packs applied to back of the neck to cool down. Patient was alert and oriented x4. Vital signs taken every 10 mins and were WNL. Patient left in stable condition with partner approximately 35 minutes after adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 16.09.2022
- Impfdatum
- 16.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Syncope
Symptomtext
Two minutes after administration of the vaccine, patient complaint of lightheaded. Legs elevated. Patient had a syncopal episode and regained consciousness in few seconds. Patient speaking coherently. VS taken. Ice pack applied, water provided. Patient verbalized of feeling better. Patient was observed for 30 minutes and left the site on stable condition
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- U
- Eingang
- 16.09.2022
- Impfdatum
- 16.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Loss of consciousness
Presyncope
Symptomtext
Few seconds after getting dose 2, client had vasovagal reaction. Patient was assisted, head protected and legs were elevated. Patient regained consciousness after 5 seconds. Ice pack was applied, water provided. Vitals signs taken X 4 and within normal limits. Patient left the site at 4:30 pm ambulatory and on stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 16.09.2022
- Impfdatum
- 16.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Dizziness
Fatigue
Immediate post-injection reaction
Nausea
Palpitations
Syncope
Symptomtext
Immediately after receiving vaccine patient reported symptoms of fatigue, nausea, dizziness, chest pain, palpitations and intermittent syncopial episodes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- 14:49 HR 68 R 18 BP 110/80 02 SAT 94% 14:54 HR 73 R 18 BP 110/80 02 SAT 97% 14:57 HR 78 R 23 BP 130/80 02 SAT 99% 15:01 HR 77 R 22 BP 134/82 02 SAT 97% 15:01 HR 92 R 22 BP 128/82 02 SAT 99%
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- U
- Eingang
- 16.09.2022
- Impfdatum
- 16.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Presyncope
Symptomtext
The patient had vasovagal reaction due to fear of needle. Patient assisted and attended to as needed per protocol. The patient was placed on flat surface and legs were elevated, cold cool packs provided to patient. Patient regained consciousness after approximate 10 seconds. Patient's vital signs were obtained 3 times every 5 minutes. Vital signs were stable. Patient was provided with water.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 15.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Dizziness
Feeling hot
Hyperhidrosis
Pallor
Presyncope
Tremor
Symptomtext
VAERS note on patient who experienced a vasovagal episode following receiving Monkeypox vaccine today 09/15/2022 at approximately 2:10 PM. Within approximately 1 minute of the administration of 0.1 ml intradermal Jynneos/BN vaccine in left forearm the client became pale and stated he was hot. He stated that he felt lightheaded. He appeared to be diaphoretic. No airway compromise was noted. No difficulty breathing noted. Client's legs were elevated onto an adjacent chair, and legs were visibly shaking when elevated to the chair. There was no loss of consciousness and no head trauma at any time. No impact injury of any kind. Client was conscious and verbalizing and answering questions appropriately through the entire experience. Client was given alcohol swab to breathe through nose while vital signs were taken on right upper arm with NIBP device at close intervals. SaO2 was measured on left index finger. Vitals were also repeated on the right arm to compare values. All VS remained within normal limits. Client stated he has never had an adverse reaction to any vaccine administration. When client stated he was feeling improved and diaphoresis had abated, client was transitioned from sitting to standing so that vital signs could be measured at each position change. The Client remained sitting for an additional 15 minutes in the vaccination room. Assessment: vasovagal response secondary to anxiety occasioned by receiving an injection. Initial right arm vital signs noted below: 2:20 PM - 89/68 sitting HR 61 SaO2 98% Serial Left arm vital signs noted below: 2:29 PM - 99/73 sitting HR 67 SaO2 100% 2:34 PM - 95/65 standing SaO2 98% 2:47PM - 100/70 standing HR 81 SaO2 99% When client felt improved and returned to prevaccination state he was transferred to postvaccination waiting area and instructed to remain for an additional 15 minutes before leaving and to communicate with postvaccination area nurses if he felt lightheaded again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- Not Applicable
- Aktuelle Erkrankungen
- None per patient
- Vorgeschichte
- None per patient
- Andere Medikamente
- Unknown
- Allergien
- None per patient
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
Patient lost consciousness for about 5 second after receiving the Second dose of Jynneos Monkeypox vaccine. Vital signs taken. first BP 94/62 , second after 5 minutes was 110/70. Other vital signs were within normal range. Patient verbalized not feeling dizzy or lightheaded and able to walk without assistance before leaving the vaccination site. Patient was observe for half an hour.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 09.09.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Pallor
Supine position
Syncope
Symptomtext
Client had syncopal episode about 2 minutes after receiving ID vaccination. Client fainted and looked paled after vaccine administration. Vital signs were initiated, ice packs were applied, client was placed in supine position with legs elevated. Client verbalized feeling better after a few minutes , however felt nausea and a bit dizzy. Was observed for additional 30 minutes until client attested to feeling better. Client left clinic feeling well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Client attested No
- Vorgeschichte
- Client attested NO
- Andere Medikamente
- Unknown
- Allergien
- Client attests to No
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 09.09.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood glucose normal
Dizziness
Loss of consciousness
Malaise
Oropharyngeal discomfort
Rash macular
Tremor
Vaccination site reaction
Symptomtext
At about 4:05 pm, patient reported feeling "not well", light headedness and throat discomfort after receiving 2nd ID monkeypox dose. RN also observed splotchy red area around the administration site. 2 additional RNs were called for assistance. EMS called. In-house physician called. At approximately 4:08, patient lost consciousness and had tremors for about 20 seconds. Patient regained consciousness without intervention. Patient was escorted from chair to examination table. BP and heart rate at 4:10 pm were 136/91, pulse 73. In- house physician arrived at 4:10 pm. EMS arrived 4:15 pm. BP and heart rate at 4:20 pm were 162/100, pulse 99, blood sugar 119. EMS transported patient to local hospital by 4:25 pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Glucose 119 at 4:20pm
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Panic disorder and ADHD.
- Andere Medikamente
- Information not provided by patient.
- Allergien
- No none allergies.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 09.09.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
After receiving vaccine patient lost consciousness for 5 seconds. regained consciousness and symptoms resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- 14:30 HR 44 R16 BP 114/70 sat 98% 14:30 HR 55R16 BP 112/66 sat 99% 14:30 HR 51 R18 BP 100/60 sat 97% 14:30 HR 49 R 18 BP 116/70 sat 98%
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Dyskinesia
Hyperhidrosis
Loss of consciousness
Pallor
Symptomtext
1 min post vaccination(5:43pm) pt complained of dizziness/lightheadedness. Water provided. Pallor noticed, pt appeared diaphoretic. LOC for approximately 7 seconds with slight jerking of limbs noted. Pt regained consciousness while still seated. Pt placed in lying position on a cot. VS initiated, WNL for pt. Ice packs applied to nape of neck and extremities. VS taken q4. Pt reported feeling better while on cot, denies any symptoms. Pt transferred to seated position at 1758, tolerated well. Pt went from standing to sitting at 1804, tolerated well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Dizziness
Hyperhidrosis
Presyncope
Symptomtext
Within 1-2 minutes of the administration of 0.1 ml intradermal Jynneos/BN vaccine in left forearm the client stated that he felt lightheaded. He appeared to be diaphoretic. No airway compromise was noted. No difficulty breathing noted. Client's legs were elevated onto an adjacent chair and from there was assisted to a supine position on the floor with feet elevated. No impact injury. Client was conscious and verbalizing and answering questions appropriately through the entire experience. Client was given alcohol swab to breathe through nose while vital signs were taken on right upper arm with NIBP device at close intervals. SaO2 was measured on right index finger. All VS remained within normal limits. Privacy screen was placed between clinic traffic and the client. Client stated (after receiving the vaccine) that he occasionally, but infrequently, feels dizzy when anxious. When client stated he was feeling improved and diaphoresis had abated, client was transitioned from supine to sitting and then standing positions with vital signs measured at each position change. Assessment: vasovagal response secondary to anxiety occasioned by receiving an injection. Serial right arm vital signs noted below: 2:23 PM - 104/65 supine HR 60 SaO2 98 120/79 supine HR 60 SaO2 99 132/91 sitting HR 58 SaO2 98 177/78 standing HR 66 SaO2 98 When client felt improved and returned to prevaccination state he was transferred to postvaccination waiting area and instructed to remain for an additional 30 minutes before leaving and to communicate with postvaccination area nurses if he felt lightheaded again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- serial concurrent vital signs
- Aktuelle Erkrankungen
- none disclosed
- Vorgeschichte
- none disclosed
- Andere Medikamente
- none disclosed
- Allergien
- none disclosed
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 06.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Contusion
Dizziness
Erythema
Fall
Loss of consciousness
Pallor
Symptomtext
Pt was sitting in chair after getting his vaccine. The patient then passed onto the floor. He was placed on a cot, pillow under his head, both legs elevated on a chair. He was given water and crackers. A red mark noted on the left side of forehead. 09/6/22 @ 1122 - Client found lying in prone position, unconscious after hearing client falling from chair. RN and LPN assisted client back to chair and client quickly regained consciousness, A&O, speech coherent, able to answer questions that was ask. Skin pallor and red bruising noted on the left forehead, skin intact. Client denied any discomfort. BP @ 1043 sitting position 100/49 pulse 53. Client drinked 1/2 water bottle during observation. Client noted to become weak not as alert. Client c/o of feeling lightheaded. RN and LPN assisted client to lie down, skin noted to become pallor BP 109/75 P 63 RR 20 in lying position @ 1050. MD called regarding situation and she responded that she will send NP to clinic. NP arrived, assessed client. Client was then able to answer all questions. Client sat up on the floor for several minutes before sitting back in chair. Client stated that he felt "fine" and denied any discomfort. A snack was given to client to eat. BP 118/82 pulse 62. Writer witnessed NP encourage client to call someone to have them be aware that client is driving along and that person need f/u. After monitoring client for 30mins, client remain A&OX3, denied any discomfort or needs. Writer escorted client to vehicle and watched him drive out of parking lot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Augmentin/Ceclor
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 03.09.2022
- Impfdatum
- 03.09.2022
- Beginn
- 03.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Dizziness
Hyperhidrosis
Hypoaesthesia
Syncope
Symptomtext
Client complained of dizziness, diaphoretic post vaccination 1 minute after. Client had an episode of syncope which lasted for few seconds. Client was then place on the cot with the legs elevated. Three sets of vital signs were taken , had varying unstable vitals, further complained of abdominal discomfort and numbness of upper and lower extremities. Cool packs and fluid offered for hydration. Patient with non-resolving symptoms. EMS was activated at 6:43 PM. EMS came and monitor at the clinic and transferred to Medical Center for further monitoring.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No existing illnesses at the time of vaccination or in the past month as stated by client.
- Vorgeschichte
- Client has no health problem or chronic condition going on.
- Andere Medikamente
- client verbalized no medication, no dietary supplements, or other herbal remedies taken at this time of vaccination.
- Allergien
- Client is allergic to Lexapro and Adderall medications. no known food allergies.
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 02.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient experienced syncopal episode after receiving Jynneos Vaccine 0.1 mL via the intradermal route. Client was assisted to the floor. Vitals: 1st attempt BP 154/77 P 54. Client recovered, was given water and monitored for 30 minutes. Repeat vitals: BP 127/70 P 60. Client left clinic at 3 pm alert and oriented.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Pain in extremity
Paraesthesia
Peripheral swelling
Ultrasound scan normal
X-ray normal
Symptomtext
I had the new COVID BOOSTER October 4, 2022, and the Monkeypox intradermally on October6, 2022. 3 days ago I realized my left hand ( monkeypox vaccination shot arm) swelled up and became quite boated. Very scary. It tingled and hurt. This never happened before. Yesterday, Urgency care sent me to ER. After X-ray, sonogram and blood draws, concussion that there was no blood cots. It was probably reaction from having the two vaccine just days apart. I had the new COVID BOOSTER October 4, 2022, and the Monkeypox intradermally on October 6, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Had blood work yesterday as well as Xray and sonogram. Emergency Room.
- Aktuelle Erkrankungen
- I had the new COVID BOOSTER October 4, 2022, and the Monkeypox intradermally on October6, 2022. My health was fine. No issues during that week.
- Vorgeschichte
- HIV/AIDS heart attack stent High Blood pressure Hip replacement POST surgery: gall bladd removal. From July 21, 2022( admission) to August 5, 2022 ( discharge)
- Andere Medikamente
- I had the new COVID BOOSTER October 4, 2022, and the Monkeypox intradermally on October6, 2022. INTELENCE TAB 200MG RITONAVIR TAB 100MG ISENTRESS TAB 400MG PREZISTA TAB 800MG. METOPROL SUC TAB 50MG ER CLOPIDOGREL TAB 75MG ROSUVASTATIN TA
- Allergien
- Seasonal allergies.
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 26.09.2022
- Impfdatum
- 24.09.2022
- Beginn
- 25.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Injection site erythema
Injection site induration
Injection site pain
Injection site swelling
Symptomtext
Overwhelming swelling and redness around injection site. Diameter of affect area is more than half of forearm. Increased firmness and tenderness. Mild chest pains.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Bumps on chest starting 2 weeks after vaccination lasting for 1 month, age 35, vaccination date 4/12/21, first Pfizer covid dose
- Staat
- VA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 19.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Chills
Cough
Diarrhoea
Fatigue
Injection site erythema
Injection site pain
Injection site swelling
Lymphadenopathy
Migraine
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
Urticaria
Symptomtext
Day after injection: swelling, redness and tenderness and the site of the injection. No noticeable wheal was present in the 24 hours following vaccination. Injection site side effects cleared within 24 hours. For 7 days following vaccination: migraine, varying fever up to 101.8?F, chills, severe fatigue, sore throat, cough and congestion (excessive mucosal drain resulting in gastro distress, namely diarrhea), swollen lymph nodes of the neck (severely so on the right side), nuchal rigidity. Managed with bed rest, acetaminophen and naproxen, and home remedies for other symptoms. All began to fully/finally resolve the morning of 9/14/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None known
- Andere Medikamente
- 10 mg Zyrtec 15 mg lexapro
- Allergien
- NKA aside from seasonal/pollen/hay
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 21.09.2023
- Impfdatum
- 27.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
Client reports another vaccine 10/25/22, but this was not at our facility. Client reports that after receiving vaccine the site on right forearm has been red with a white center. It gets redder sometimes and some times is raised. He has sought advice from PCP but no interventions. Hoping to have someone contact him about whether his reaction is normal or something to worry about.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic illnesses include HIV, diabetes, CHF and CKD
- Andere Medikamente
- Triumeq, Singulair, coreg, insulin, Crestor, Ambien
- Allergien
- doxycycline and dye contrast
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 23.06.2023
- Impfdatum
- 13.06.2023
- Beginn
- 14.06.2023
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Injection site pruritus
Injection site scar
Injection site swelling
Injection site warmth
Symptomtext
24 hours after the left forearm intradermal injection, he had swollen, itching, painful, burning, hot to touch (no drainage) areas around the injection site that is "spiraling up to my shoulder". It is only affecting his left side. Advised treatment: cool compresses, Ibuprofen 400-600mg with food every 6-8 hours, can take Zyrtec or Benadryl as directed for swelling and itching, follow up with PCP or urgent care if continues to worsen. 6/23/23 spoke to patient today and symptoms have resolved. There is a little scar where the injection itself entered his skin on forearm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unsure
- Vorgeschichte
- Unsure
- Andere Medikamente
- Unsure
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 16.06.2023
- Impfdatum
- 18.05.2023
- Beginn
- 18.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Pain
Pyrexia
Symptomtext
On 6/15/23, the patient returned for his second dose MPV vaccine. Upon assessing the patient, he told the RN that he had received his first shot (on 5/18/2023) via IM route in the left deltoid. He reported that after vaccination on 5/18, he had fatigue, body aches and a perceived fever. No other side effects were given. The site where he received the vaccine was WNL, without pain or any evidence of injury. Second dose was administered SQ per CDC guidelines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Unknown.
- Vorgeschichte
- Unknown.
- Andere Medikamente
- Unknown.
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 13.12.2022
- Impfdatum
- 09.12.2022
- Beginn
- 11.12.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint swelling
Pruritus
Urticaria
Symptomtext
Swelling of Joints (Both knees) Hives/itching on back
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Chronic Sinitisis
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Motrin 200mg
- Allergien
- penicillin/amoxicillin
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 08.12.2022
- Impfdatum
- 05.12.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Diarrhoea
Feeling hot
Hyperhidrosis
Illness
Productive cough
Pyrexia
Vomiting
Symptomtext
I was on a vacation for a week ending on 12/3/22 and my roommate had a cough and runny nose, I didn't feel anything but was likely primed for whatever he had. The illness I have had from 12/5-12/8 has been the worst experience of my life. At one point a solid 10, currently a 5. Liquid from both ends. Couldn't keep food in. 101.7 fever for 2 days, hot sweats, terrible productive coughing to the point of pain. Several vomiting sessions mid sleep. The roommate has recovered and had none of the symptoms I did. 2 other people I have infected (my spouse and another guy) also did not have the extreme symptoms I did. I received my flu vaccine in September.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- I was on a vacation for a week ending on 12/3/22 and my roommate had a cough and runny nose, I didn't feel anything but was likely primed for whatever he had. The illness I have had from 12/5-12/8 has been the worst experience of my life. At one point a solid 10, currently a 5. Liquid from both ends. Couldn't keep food in. 101.7 fever for 2 days, hot sweats, terrible productive coughing to the point of pain. Several vomiting sessions mid sleep. The roommate has recovered and had none of the symptoms I did. 2 other people I have infected (my spouse and another guy) also did not have the extreme symptoms I did. I received my flu vaccine in September.
- Vorgeschichte
- High blood pressure and cholesterol.
- Andere Medikamente
- Lisinopril, Naltrexone, Truvada, Vitamin B Complex
- Allergien
- English Ivy sap
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- -
- Geschlecht
- M
- Eingang
- 25.11.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Incorrect route of product administration
Injection site pruritus
Rash macular
Urticaria
Symptomtext
Red patches around body, they looked like hives, but no irruption, they were just red spots; fever; Jynneos was administered intradermal; The patient received the Jynneos vaccine and it itched really bad; Chills; Case reference number US-BN-2022-002652 is a spontaneous case report initially received on 21-Sep-2022 from other health professional via Agency (reference number: USBAV22-1479) and concerns 51-year-old male patient. The patient's medical history included a reaction to a COVID-19 vaccine (further described as 'got really sick'). The patient's concomitant medication details were not provided. Previous vaccines included COVID-19 vaccine (brand name unknown), at an unknown dose, site or route of administration, for unknown indication. On 07-Sep-2022, the patient was vaccinated with the first dose of Jynneos (smallpox and monkeypox vaccine, live, nonreplicating; batch number: FDP00019) at an unknown dose, administered intradermal at an unknown site of administration for monkeypox prophylaxis (explicitly coded as 'intradermal injection'). On the same day, the patient's injection site itched really bad. On an unspecified date, reported as 'three to four days later', the patient developed some red patches around body, which looked like hives, but no irruption, they were just red spots on patient's trunk that spread to arms and legs and were then on face (looked like had acne). They did not itch. On an unspecified date, the patient took Benadryl, had fever of 98.9 degrees Fahrenheit and chills for two days. On an unspecified date, the events of 'fever' and 'chills' were resolved. The patient stated that his trunk doesn't look bad as it was. At the time of this report, the outcome for the event of 'injection site itching' was unknown and for the event of 'redness' and 'hives' was recovering/resolving. The reporter assessed these events as non-serious and possibly related to the Jynneos.. Additional information received on 21-Sep-2022 included local BN case ID.; Reporter's Comments: A 51-year-old male patient experienced the non-serious event of injection site pruritus, on the same day following vaccination with first dose of Jynneos, applied intradermally for monkeypox prophylaxis (explicitly coded as intradermal injection). Three or four days following the dose administration, the patient experienced the non-serious event of urticaria-like rash. The patient also experienced the non-serious events of chills and fever. The patient took Benadryl. Fever and chills had resolved, the urticaria-like rash had improved. Outcome for injection site pruritus was unknown. Urticaria is listed per CCDS V1.0 but unlisted per the PI for Jynneos. Injection site pruritus, chills and fever are listed per PI and CCDS. Intradermal injection is considered listed per company convention. The patient's medical history included a past reaction to a COVID-19 vaccine. Concomitant medications were unknown, but past vaccines included COVID-19 vaccine. Considering the known safety profile of Jynneos, the events are assessed as related to the suspect vaccine. Intradermal injection is not related to Jynneos, but to the human factor.; Sender's Comments: A 51-year-old male patient experienced the non-serious event of injection site pruritus, on the same day following vaccination with first dose of Jynneos, applied intradermally for monkeypox prophylaxis (explicitly coded as intradermal injection). Three or four days following the dose administration, the patient experienced the non-serious event of urticaria-like rash. The patient also experienced the non-serious events of chills and fever. The patient took Benadryl. Fever and chills had resolved, the urticaria-like rash had improved. Outcome for injection site pruritus was unknown. Urticaria is listed per CCDS V1.0 but unlisted per the PI for Jynneos. Injection site pruritus, chills and fever are listed per PI and CCDS. Intradermal injection is considered listed per company convention. The patient's medical history included a past reaction to a COVID-19 vaccine. Concomitant medications were unknown, but past vaccines included COVID-19 vaccine. Considering the known safety profile of Jynneos, the events are assessed as related to the suspect vaccine. Intradermal injection is not related to Jynneos, but to the human factor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: 98.9 degrees Fahrenheit; Comments: /
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 vaccination; Reaction to previous exposure to any vaccine
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 23.11.2022
- Impfdatum
- 25.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acne
Haemorrhage
Injection site pain
Injection site vesicles
Malaise
Skin lesion
Viral test
Symptomtext
Patient developed painful large blister over primary injection site. He also developed small lesions throughout body (back, arms, legs, chest). Some appeared pimple like, some slightly bloody. General malaise but no fevers. I believe he may have gotten secondary reaction/monkeypox.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- pictures taken of healing lesions (11/23/2022). Monkeypox swab submitted (11/23/2022).
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- migraines
- Andere Medikamente
- apretude, imitrex
- Allergien
- shellfish, cats, lactose
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 14.11.2022
- Impfdatum
- 18.09.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site inflammation
Injection site pruritus
Injection site scar
Injection site swelling
Injection site urticaria
Mechanical urticaria
Urticaria
Symptomtext
In the few days following getting my second MPV dose, my forearm became increasingly more inflamed. At the peak of the inflammation, the swelling took over about 80% of my entire forearm around the injection site. About two or three weeks after this vaccine, the swelling was gone and only a scar was left. However, hives appeared around my injection site (within the bounds of where the swelling was, which was most of my forearm). These weren't very itchy, but they looked very bad, and keep reoccurring. I also noticed I started having dermatographia at this time. Raised welts that looks like scratch marks usually appear on my buttocks, thighs, and sometimes on my upper arms. It has been 2 months since I got this MPV dose, but these hives consistently continue to reappear every 5-7 days. I have pictures of these described symptoms. I am concerned that this vaccine caused some sort of allergy or autoimmune issue to flare up, and find it odd that the hives keep flaring up intensely every 5-7 days, only on the forearm where I had intradermal injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site inflammation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Mango
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 09.11.2022
- Beginn
- 09.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site discharge
No adverse event
Symptomtext
Vaccine leaked from the injection site. The dose was repeated intradermally and was successful. No adverse even occurd.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discharge
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- COVID-19
- Vorgeschichte
- None indicated
- Andere Medikamente
- Finasteride, Claritin
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 31.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- ID / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site infection
Injection site pain
Injection site swelling
Symptomtext
Patient developed cellulitis-like reaction (redness, swelling, pain) at injection site a few days after vaccination. She sought medical care and received antibiotics for the infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 23.09.2022
- Beginn
- 25.09.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Contusion
Erythema
Furuncle
Pruritus
Swelling
Vaccination site induration
Vaccination site pain
Symptomtext
Patient states within 48 hours after receiving vaccine, swell and itch, turned bright red, looked like a boil. Lasted at least 3 and half weeks. Following decrease of redness, ring in 2-3 inches of diameter in 4th week. Hard core at site of vaccination. Site specific achiness, ache in elbow/possible referred pain. 5th week from 1st vaccination, still showing visible signs of bruising. No other vaccine on day of MPV vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- No medical tests/ lab tests
- Aktuelle Erkrankungen
- Patient denies
- Vorgeschichte
- Patient denies
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 22.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pruritus
Vaccination site erythema
Vaccination site induration
Vaccination site infection
Symptomtext
Client states he woke up the day after receiving vaccine "and had a streaking red infection" near the site of vaccine administration. Client states he did "find myself scratching it several times during the night because it itched and I think I may have broken it open". Client went to the Emergency Department on 10/22 and was prescribed oral Keflex 500 mg 4 times a day for seven days. He states "it has cleared up nicely".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- 10/11/22 - Covid 19 diagnosis Current sinus infection
- Vorgeschichte
- Joint pain
- Andere Medikamente
- Ritalin Vit D Supplement Wellbutrin Vibryd Sudafed Zyrtec
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 07.10.2022
- Impfdatum
- 31.08.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Nausea
Skin warm
Tenderness
Vomiting
Symptomtext
Per patient, 1 day after received vaccine, he developed bright red streaking going up his arm, and it went past his elbow, over 8 inches in length. Was warm to touch and tender. Also had nausea and vomiting 2 days after administration of vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- Unsure, I believe patient was seen at his PCP
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 01.10.2022
- Impfdatum
- 25.09.2022
- Beginn
- 26.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Fatigue
Headache
Myalgia
Nausea
Peripheral swelling
Symptomtext
Severe chills, headache, Nausea, Muscle Aches. Fatigue as well as severe swelling, reddening, in large part of left forearm starting about 12 hours after injection and lasting to some degree for 48-72 hours after.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma
- Andere Medikamente
- none
- Allergien
- motrin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 23.09.2022
- Impfdatum
- 26.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Contusion
Erythema
Induration
Pruritus
Skin exfoliation
Symptomtext
itching, redness, peeling, indurated area/bruising still present 4 weeks later
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 21.09.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site discharge
Symptomtext
No Wheal and observed leakage on first Intradermal administration attempt. Successful 2nd administration subcutaneously.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discharge
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 19.09.2022
- Impfdatum
- 15.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site rash
Injection site swelling
Injection site vesicles
Symptomtext
Redness and itchiness at injection site on the first day, which turned into a large blister and larger area of redness, itchiness, and swelling, The blister popped 36 hours after injection, but the rash spread for another day. The rash directly surrounding the blister was also painful and swollen, while the larger rash was just itchy on Friday and Saturday (day 2 and 3). It is less itchy and swollen today (day 4), but still a large red rash, with the section around the former blister still sore to the touch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- post COVID syndrome fibromyalgia IBS
- Andere Medikamente
- Zyrtec, Cymbalta, Singulair, Concerta, multivitamin
- Allergien
- Penicillin, insect venom
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 05.09.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site discolouration
Injection site swelling
Keloid scar
Symptomtext
Permanent, raised, discolored keloid scar formed at site of the intradermal injection and has not went away .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discolouration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 15.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site discharge
Symptomtext
Vaccinator attempted to vaccinate client with Monkeypox Jynneos 0.1ml intradermally in L arm. There appeared to be leakage on site. Another successful attempt was performed on R forearm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discharge
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 15.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Injection site discharge
Symptomtext
Vaccine given ID in R forearm. Leakage occurred. Vaccine re-administered 2 inches from 1st. No leakage. Dose administered successfully.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discharge
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 15.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site discharge
Vaccination error
Symptomtext
No Wheal and observed leakage on first Intradermal administration attempt. Successful 2nd administration subcutaneously.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discharge
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Urticaria
Symptomtext
1st intradermal shot did not create a wheal. 2nd intradermal injection created wheal. Pt left in no distress from injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Urticaria
Symptomtext
1st intradermal shot did not create a wheal. 2nd intradermal injection created wheat. Pt left in no distress from injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Urticaria
Symptomtext
1st intradermal shot did not create a wheal. 2nd intradermal injection created wheal. Pt left in no distress from injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Injection site erythema
Injection site oedema
Pruritus
Symptomtext
10:35 AM Assessed erythema and edema approximately the size of a half dollar around the injection site. There was no dizziness, SOB, chest discomfort, edema of the lips, throat, tongue per Patient. He states that pruritis started immediately post-vaccine but went away. No systemic symptoms of hypersensitivity noted and remained localized throughout observation. Provided Diphenhydramine 25 mg. po x 1 and famotidine 40 mg. po x 1 after determined that patient had taken treatment prior without incident. Observed client for a total of 30 minutes and discharged to home. Had a driver with patient who was driving. Gave post discharge instructions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
First attempt at wheal not achieved, second attempt needed, wheal achieved on second attempt successfully.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Unknown.
- Vorgeschichte
- Unknown.
- Andere Medikamente
- Unknown.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 30.08.2022
- Beginn
- 06.09.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Urticaria
Symptomtext
Received called that the area of injection site was red, small whelps noted below injection site that looked like "ant bites" . Called health department medical director, she recommended he be seen by primary care provider for evaluation, if unable to be seen for evaluation, try Benadryl if rash is itchy or looks to him like hives. I called and spoke with "friend" patient's language is okay, Explained and friend states "he is at work". I called today at 7:30 to check on him again. VAERS form filled out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None as of 9/7/2022
- Aktuelle Erkrankungen
- Denies "Are you currently sick/ill. Answered no to Heart disease (e.g. coronary artery disease or cardiomyopathy); Hypertension, Diabetes, hypercholesterolemia, first-degree relative diagnosed with heart disease at age 50 or younger, smoking
- Vorgeschichte
- unknow, answered NO to above questions
- Andere Medikamente
- Answered no to questions on form: "ever had serious allergic reaction to JYNNEOS vaccine, including benzonase, tromethamine, gentamycin, ciprofloxacin, or chicken/egg protein (and are currently avoiding exposure to all chicken or egg produ
- Allergien
- Answer no to questions on form.
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 03.09.2022
- Impfdatum
- 03.09.2022
- Beginn
- 03.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Incorrect dose administered
Injection site extravasation
Wrong technique in product usage process
Symptomtext
Injected the 0.1 dose of vaccine to the site but upon removal of needle, a large amount of the vaccine leaked out of the wheal and the wheal flattened immediately, leaving a flattened blanched area in the skin. Due to not knowing how much of the dose actually remained inside the wheal area, the vaccine was re-administered using the Subcutaneous method in the posterior Left upper arm. Patient reported no pain at the initial intradermal injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site extravasation
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none per patient statement
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- NKDA or other allergies per patient statement
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 02.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
Administered .1cc JYNNEOS vaccine- no wheal appeared. Explained about necessity of wheal to patient, and he consented to another dose. Administered another .1cc of JYNNEOS vaccine- small wheal appeared.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 01.09.2022
- Impfdatum
- 30.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Induration
Pruritus
Skin warm
Urticaria
Symptomtext
did not get a wheal with first intradermal injection and was given a 2nd intradermal injection. Developed 2 itchy welts, measuring approximately 40mm each that are warm to touch and indurated. No other side effects noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- long COVID, asthma
- Andere Medikamente
- lexapro, metoprolol, pepcid
- Allergien
- treenuts, shellfish
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 01.09.2022
- Impfdatum
- 26.08.2022
- Beginn
- 28.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site scab
Injection site swelling
Injection site vesicles
Symptomtext
Development of lesion at the inoculation site: Redness, swelling, and a raised, fluid filled sore that has began to scab over
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Accutane (Isotretinoin)
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 01.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Urticaria
Symptomtext
Vaccinator was unable to obtain a wheal with the first attempt at vaccination. On the 2nd attempt vaccinator obtained a wheal. Second attempt was 2 inches away from the 1st stick on the same arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 01.09.2022
- Impfdatum
- 30.08.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Injection site erythema
Injection site inflammation
Injection site pruritus
Injection site swelling
Skin swelling
Symptomtext
JYNNEOS vaccine given at 1pm on 8/30/2022. Started having intense liquid diarrhea 3 hours after the vaccine (different than previous food/IBS related diarrhea I've had in the past). Continued to have diarrhea 4 additional times for the next 12 hours even after taking pepto and immodium. Diarrhea subsided the next day after additional immodium was taken. In addition, the injection site became itchy, red, and swollen on 8/31/2022 and became puffy even after taking an antihistamine. It's currently 9/1/2022 and injection site is inflamed, red, swollen, and itchy. Using wrapped ice pack and anti-itch cream.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Vitamin D, B12, and birth control pills
- Allergien
- intolerance to apples
- Vorherige Impfungen
- Swollen lymph node in collarbone area after Pfzier Covid booster May 2022, last a couple weeks.
- Staat
- VA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 01.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site mass
Injection site pain
Injection site pruritus
Symptomtext
When I got the injection the nurse said I had a normal "well" I believe she called it. It looked like a mosquito bite. She said it would probably go away after 3-5 hours. It has been 24 hours and the injection site has formed a large red lump that is very itchy and a bit painful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Buspirone, Emtricitabine/Tenof
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 30.08.2022
- Impfdatum
- 29.08.2022
- Beginn
- 29.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Dizziness
Hyperhidrosis
Nausea
Vomiting
Symptomtext
Patient came in yesterday for his first dose of monkeypox. Post monkey pox adm. during observation period patient stated to feel lightheadedness, diaphoretic, and with nauseous and throwing up.. V/S and BS taken, Water, cookies, and icepacks give,. Patient states he didn't eat that morning and usually gets anxious with certain things. One of our family medicine providers did see him and recommended to go to ER pt refused. Patient got put on Dr schedule to do a more detailed eval. Followed up with the patient this morning and he states he is doing much better and feels great.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Blood sugar 08/29/22: 126 Vital signs 08/29/22: BP:123/70, P: 65, RR:17, SPO2: 99% room air
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 20.08.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
2 days after the injection, small bumps started to appear on my right arm (the injection arm). These were initially dismissed as bug bites. However, over the next few days, more bumps started to appear only on my right arm (elbow region, right arm and forearm) and nowhere else on my body. The existing bumps continues to enlarge and all bumps appears to be identical in shape and color.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HIV infection
- Andere Medikamente
- Odefsey
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 22.08.2022
- Impfdatum
- 21.08.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site inflammation
Injection site pruritus
Symptomtext
Raised, red, itchy area around the injection site (~1? in total diameter) starting about 12-16 hours after administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression, OCD, HSV-2
- Andere Medikamente
- Venlafaxine 150mg once daily, Buspirone 15mg twice daily, valacyclovir 1000mg once daily, Descovy once daily
- Allergien
- None
- Vorherige Impfungen
- Fatigue and myalgia at 33yo after Moderna SARS-CoV 2 vaccine 3/10/21 lot 026A21A and 04/06/2021 lot# 020B21A
- Staat
- MD
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 14.08.2022
- Beginn
- 14.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site pain
Vaccination site swelling
Symptomtext
About 3 hours after the vaccination was administered I felt a stinging pain at the vaccination site on my left back arm. Since then, the vaccination site has had this stinging pain. It feels like I was stung by a bee. The vaccination site has a slight bump and looks like there is a straight cut going right throught the middle of it. The top of the bump looks like a boil that bursted. I have received the vaccination 48 hours ago and although the symptoms have not worsened, it has remained static. A stinging pain in my arm. I have kept the site clean and continue to apply neosporin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- None were completed.
- Aktuelle Erkrankungen
- none.
- Vorgeschichte
- HIV, Carpel Tunnel, Sciatica,
- Andere Medikamente
- Biktarvy, Sertraline, Gabapentin, Vitamin D
- Allergien
- Bactrim, Amoxicillin, Skin of mangoes
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 18.07.2023
- Impfdatum
- 20.04.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
33 patients received Jynneos after the beyond use date of 19-Apr-2023; Jynneos vaccine administered intradermally at 0.1 mL; The patient received the second dose of Jynneos 13 days after the first dose; Case reference number US-BN-2023-000959 is a spontaneous case report initially received on 23-May-2023 from a nurse via Communication (reference number: USBAV23-0685) and concerns *33* patients of unknown gender. The patients were born on 12-May-1962 (61 years), 26-Aug-1998 (24 years), 03-Apr-1985 (38 years), 24-May-1995 (27 years), 06-Oct-1997 (25 years),14-Apr-1991 (32 years), 23-Oct-1986 (36 years), 04-Apr-1990 (33 years), 08-Aug-1959 (63 years), 29-Sep-1975 (47 years), 26-Nov-1978 (44 years), 31-Jul-1996 (26 years), 06-Feb-1972 (51 years), 03-Sep-1991 (31 years), 08-May-1961 (62 years), 24-Sep-1963 (59 years), 05-Jan-1985 (38 years), 23-Jan-1964 (59 years), 02-Oct-1970 (52 years), 21-Jan-1962 (61 years), 24-Jul-1964 (58 years), 21-Aug-1962 (60 years), 26-Jul-1953 (69 years), 25-Apr-1995 (28 years), 25-Feb-1966 (57 years), 30-Mar-1976 (47 years), 05-Aug-1964 (58 years), 12-Feb-1980 (43 years), 01-Dec-1991 (31 years), 16-Feb-1986 (37 years), 22-Jul-1988 (34 years), 05-Jun-1998 (24 years) and on 25-Mar-1956 (67 years). The patients' medical history and concomitant medication details were not provided. On 20-Apr-2023, two patients were vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with beyond use date (BUD) on 19-Apr-2023, at a dose of 0.1 mL, administered intradermally in the *left forearm*, for monkeypox (explicitly coded as 'expired vaccine used' and 'intradermal injection') and one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously, in the *left upper arm*, for monkeypox (explicitly coded as 'expired vaccine used'). On 21-Apr-2023, one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.1 mL, administered intradermally in the *left forearm*, for monkeypox (explicitly coded as 'expired vaccine used' and 'intradermal injection') and one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD) on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously, in the *left upper arm*, for monkeypox (explicitly coded as 'expired vaccine used'). On 24-Apr-2023, one patient was vaccinated with the *first dose* of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously, in the *left upper arm*, for monkeypox (explicitly coded as 'expired vaccine used'). On 25-Apr-2023, one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously in the *left upper arm*, for monkeypox (explicitly coded as 'expired vaccine used'). On 26-Apr-2023, one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD) on 19-Apr-2023, at a dose of 0.1 mL, administered intradermally in the *left forearm*, for monkeypox (explicitly coded as 'expired vaccine used' and 'intradermal injection'). On 27-Apr-2023, three patients were vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.1 mL, administered intradermally in the *left forearm*, for monkeypox (explicitly coded as 'expired vaccine used' and 'intradermal injection'). On 28-Apr-2023, one patient was vaccinated with the *first* dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously, in the *left upper arm*, for monkeypox (explicitly coded as 'expired vaccine used'). On 02-May-2023, one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.1 mL, administered intradermally in the *left forearm*, for monkeypox (explicitly coded as 'expired vaccine used' and 'intradermal injection') and one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously, in the *left upper arm*, for monkeypox (explicitly coded as 'expired vaccine used'). On 04-May-2023, one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously, in the *left upper arm*, for monkeypox (explicitly coded as 'expired vaccine used'). On 05-May-2023, three patients were vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.1 mL, administered intradermally in the *left forearm*, for monkeypox (explicitly coded as 'expired vaccine used' and 'intradermal injection'). On 09-May-2023, one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.1 mL, administered intradermally in the *left forearm*, for monkeypox (explicitly coded as 'expired vaccine used' and 'intradermal injection'). On 10-May-2023, one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.1 mL, administered intradermally in the *left forearm*, for monkeypox (explicitly coded as 'expired vaccine used' and 'intradermal injection') and one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously, in the left *upper arm*, for monkeypox (explicitly coded as 'expired vaccine used'). On 11-May-2023, *13 days after the first dose of Jynneos (administered on 28-Apr-2023), the patient was vaccinated with the second dose of Jynneos (batch number: FDP00019; expiration date: Oct-24) (explicitly coded as 'Inappropriate schedule of vaccine administered')* and two patients were vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously, in the *left upper arm*, for monkeypox (explicitly coded as 'expired vaccine used'). On 15-May-2023, two patients were vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously, in the *left upper arm*, for monkeypox (explicitly coded as 'expired vaccine used'). On 16-May-2023, one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.1 mL, administered intradermally in the *left forearm*, for monkeypox (explicitly coded as 'expired vaccine used' and 'intradermal injection'). On 17-May-2023, two patients were vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.1 mL, administered intradermally in the *left forearm*, for monkeypox (explicitly coded as 'expired vaccine used' and 'intradermal injection') and one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously, in the *left upper arm*, for monkeypox (explicitly coded as 'expired vaccine used'). On 18-May-2023, one patient was vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously, in the *left upper arm*, for monkeypox (explicitly coded as 'expired vaccine used'). On 22-May-2023,*28 days after the first dose (administered on 24-Apr-2023) the patient was vaccinated with the second* dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.5 mL, administered subcutaneously, in the *left upper arm*, for monkeypox (explicitly coded as 'expired vaccine used') and three patients were vaccinated with a dose of Jynneos (batch number: FDP00019; expiration date: Oct-24), with BUD on 19-Apr-2023, at a dose of 0.1 mL, administered intradermally in the *left forearm*, for monkeypox (explicitly coded as 'expired vaccine used' and 'intradermal injection'). As reported, Jynneos vaccine was stored correctly at refrigerator temperatures with no excursions and that that was in an outpatient clinic, contributing factors were human error on data entry into electronic medical record (EMR) and at time of administration, and system design of both EMR which did not allow for both BUD and expiration dates, and packaging design of the vaccine which also made it hard to have a BUD on each vial. At the time of *this follow up report*, the patients *did not experience* any adverse event due to Jynneos vaccination. Additional information received on 24-May-2023 included local case ID number. All follow-up information is blended into the case narrative above, with the latest information presented between asterisks (*). Follow-up information received from the nurse on 16-Jun-2023: New information included date of birth and age for 33 patients with vaccination dates, indication, dosages and routes of Jynneos administrations. All follow-up information is blended into the case narrative above, with the latest information presented between asterisks (*). Follow-up information received from the reporter on 28-Jun-2023: New information included site of administration for each dose administered, confirmation that two patients received two expired doses of Jynneos which caused additional non-event to be added and confirmation that no patient experienced any adverse event due to Jynneos.; Reporter's Comments: This case concerns 35 adult patients (aged between 24 and 69 years old) of unspecified gender who were vaccinated with Jynneos at an unknown site of administration, for monkeypox. The patients received vaccines from batch FDP00019 with beyond use date (BUD) prior to the dates of vaccination, which is considered expired product administered. 19 patients received Jynneos at a dose of 0.1 mL, intradermally (which is considered intradermal injection). Reportedly, one patient was vaccinated with the second dose of Jynneos on the day 13 after the first dose, which is considered as inappropriate schedule of vaccine administered. 16 patients received subcutaneous Jynneos at a dose of 0.5 mL. Reportedly, the vaccines were stored correctly at refrigerator temperatures with no excursions. No associated adverse events were reported. Expired product administered, inappropriate schedule of vaccine administered and intradermal injection are considered listed per company convention. The patients' medical history and concomitant medication details were not provided. Causality is assessed as not related to suspect product but to human factor. The case is non-serious.; Sender's Comments: This case concerns 35 adult patients (aged between 24 and 69 years old) of unspecified gender who were vaccinated with Jynneos at an unknown site of administration, for monkeypox. The patients received vaccines from batch FDP00019 with beyond use date (BUD) prior to the dates of vaccination, which is considered expired product administered. 19 patients received Jynneos at a dose of 0.1 mL, intradermally (which is considered intradermal injection). Reportedly, one patient was vaccinated with the second dose of Jynneos on the day 13 after the first dose, which is considered as inappropriate schedule of vaccine administered. 16 patients received subcutaneous Jynneos at a dose of 0.5 mL. Reportedly, the vaccines were stored correctly at refrigerator temperatures with no excursions. No associated adverse events were reported. Expired product administered, inappropriate schedule of vaccine administered and intradermal injection are considered listed per company convention. The patients' medical history and concomitant medication details were not provided. Causality is assessed as not related to suspect product but to human factor. The case is non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- M
- Eingang
- 14.06.2023
- Impfdatum
- 01.02.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Inappropriate schedule of product administration
No adverse event
Symptomtext
The second dose of Jynneos vaccine was used eight weeks beyond use date; The patient received the second dose of Jynneos on 64 day; Case reference number US-BN-2023-000949 is a spontaneous case report initially received from a health care professional (reference number: USBAV23-0703) on 30-May-2023 and concerns a male patient of unknown age. The patient's medical history and concomitant medication details were not provided. On 01-Feb-2023, the patient was vaccinated with the first dose of Jynneos (batch number: FDP00019; expiration date: 31-Oct-2024), at a dose of 0.5 milliliter, subcutaneously, at an unknown site of administration, for smallpox/monkeypox prophylaxis. On 06-Apr-2023, 64 days after the first dose of Jynneos, the patient was vaccinated with the second dose of Jynneos (batch number: FDP00019; expiration date: 31-Oct-2024), at a dose of 0.5 milliliter, subcutaneously, at an unknown site of administration (explicitly coded as 'inappropriate schedule of vaccine administered'). It was reported that vaccine was used eight weeks beyond use date (explicitly coded as 'expired vaccine used'). At the time of the initial report, it was unknown if the patient experienced any adverse event due to Jynneos vaccination. Additional information received from Bavarian Nordic on 31-May-2023, included local case ID.; Reporter's Comments: A male patient of unknown age was vaccinated with the second dose of Jynneos, at a dose of 0.5 milliliter, subcutaneously, at an unknown site of administration (considered as inappropriate schedule of vaccine administered). It was reported that vaccine was used eight weeks beyond use date (considered as expired vaccine used). Expired product administered and inappropriate schedule of product administration are both considered listed per company conventions. At this point, it was unknown if the patient experienced any adverse event due to Jynneos vaccination. The patient's medical history and concomitant medication details were not provided. Expired product administered and inappropriate schedule of product administration are both assessed as not related to suspect product but to human factor. The case is non-serious.; Sender's Comments: A male patient of unknown age was vaccinated with the second dose of Jynneos, at a dose of 0.5 milliliter, subcutaneously, at an unknown site of administration (considered as inappropriate schedule of vaccine administered). It was reported that vaccine was used eight weeks beyond use date (considered as expired vaccine used). Expired product administered and inappropriate schedule of product administration are both considered listed per company conventions. At this point, it was unknown if the patient experienced any adverse event due to Jynneos vaccination. The patient's medical history and concomitant medication details were not provided. Expired product administered and inappropriate schedule of product administration are both assessed as not related to suspect product but to human factor. The case is non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: None.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 17.05.2023
- Beginn
- 17.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 18.05.2023
- Beginn
- 18.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 20.04.2023
- Beginn
- 20.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 16.05.2023
- Beginn
- 16.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 02.05.2023
- Beginn
- 02.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 22.05.2023
- Beginn
- 22.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 22.05.2023
- Beginn
- 22.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passes. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 09.05.2023
- Beginn
- 09.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 25.04.2023
- Beginn
- 25.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 12.06.2023
- Impfdatum
- 04.05.2023
- Beginn
- 04.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 27.04.2023
- Beginn
- 27.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passes. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 10.05.2023
- Beginn
- 10.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 21.04.2023
- Beginn
- 21.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 27.04.2023
- Beginn
- 27.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 24.04.2023
- Beginn
- 24.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 26.04.2023
- Beginn
- 26.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 12.06.2023
- Impfdatum
- 11.05.2023
- Beginn
- 11.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 17.05.2023
- Beginn
- 17.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 27.04.2023
- Beginn
- 27.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passes. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 17.05.2023
- Beginn
- 17.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 15.05.2023
- Beginn
- 15.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 05.05.2023
- Beginn
- 05.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 05.05.2023
- Beginn
- 05.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD pass. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 11.05.2023
- Beginn
- 11.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 10.05.2023
- Beginn
- 10.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 20.04.2023
- Beginn
- 20.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 15.05.2023
- Beginn
- 15.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD passed. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 02.05.2023
- Beginn
- 02.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD past. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 05.05.2023
- Beginn
- 05.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD past. DUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 20.04.2023
- Beginn
- 20.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD past. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 28.04.2023
- Beginn
- 28.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD past. BUD was 4/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 22.05.2023
- Beginn
- 22.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered after BUD past. BUD was 4/19/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 18.01.2023
- Beginn
- 18.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
It was noted later that no new vaccine vial was removed the day the vaccine was administered; presume that vial from previous day was used. The vial was kept at appropriate refrigerated temperature but punctured on 1/17/23 (more than 8 hours prior). Patient was notified, offered a repeat vaccine, though she declined a repeat vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 18.01.2023
- Beginn
- 18.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
It was noted later that no new vaccine vial was removed that day the vaccine was given; presume that vial from previous day was used. The vial was kept at appropriate refrigerated temperature but punctured on 1/17/23 (more than 8 hours prior). Patient was notified and agreed to schedule a follow up vaccine dose appointment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 18.01.2023
- Beginn
- 18.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
It was noted later that no new vaccine vial was removed that day; presume that vial from previous day was used. The vial was kept at appropriate refrigerated temperature but punctured on 1/17/23 (more than 8 hours prior). Patient was notified and agreed to schedule a follow up vaccine dose appointment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 19.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Contusion
Skin induration
Skin mass
Symptomtext
Patient was vaccinated on 8/19/2022. He reported to the MPX clinic on 8/31/22 to inform the staff that he had been diagnosed with Cellulitis by his PCP. The patient reports he developed a hard knot with bruising on his right arm, that eventually spread through out the entire arm. The patient further reports he was prescribed antibiotics for treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 22.12.2022
- Impfdatum
- 14.12.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect route of product administration
Symptomtext
Patient is 17 years old and was administered an intradermal vaccine instead of recommended subcutaneous vaccine for people <18 years old
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Freezer vaccine had been stored in had been unplugged and temperature monitoring of the vaccine was not done prior to administering to the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Freezer that the vaccine had been stored in had been turned off and temperature monitoring not done prior to administering to patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Freezer that vaccine was stored in was turned off and temperature was not being monitored until after the vaccine was administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Pt believed her second dose due 12/5/22 - was inadvertently given that day. Actual due date of second dose is 12/12/22. Patient notified, is feeling fine. Will not repeat dose per guidelines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- NONE.
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- M
- Eingang
- 25.11.2022
- Impfdatum
- 07.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Incorrect route of product administration
Symptomtext
The second dose of Jynneos administered 23 days after the first dose; Jynneos vaccine administered intradermally; Case reference number US-BN-2022-003742 is a spontaneous case report initially received on 30-Sep-2022 from a nurse via Communications (reference number: USBAV22-1587) and concerns a male patient. The patient's medical history and concomitant medication details were not reported. On 07-Sep-2022, the patient was vaccinated with the first dose of Jynneos (smallpox and monkeypox vaccine, live, nonreplicating; batch number: FDP00019), at a dose reported as 0.1 ml, intradermally, for monkeypox prophylaxis (explicitly coded as 'intradermal injection'). On 30-Sep-2022, 23 days after the first dose, the patient was vaccinated with the second dose of Jynneos (batch number: FDP00019), at a dose reported as 0.1 ml, intradermally (explicitly coded as 'inappropriate schedule of vaccine administered' and 'intradermal injection'). At the time of this report, it was unknown if the patient experienced any adverse event due to Jynneos. Additional information received from Bavarian Nordic on 03-Oct-2022 included the local BN case ID.; Reporter's Comments: A male patient born in 1985 was vaccinated with the first dose of Jynneos, at a dose reported as 0.1 ml, intradermally, for monkeypox prophylaxis, which is considered as intradermal injection. Reportedly, on the day 23 after the first dose, the patient was vaccinated with the second dose of Jynneos, at a dose reported as 0.1 ml, intradermally, which is considered as inappropriate schedule of vaccine administered and intradermal injection. At the time of this report, it was unknown if the patient experienced any adverse event due to Jynneos. Intradermal injection and inappropriate schedule of product administration are considered as listed per company convention. The patient's medical history and concomitant medication details were not reported. Intradermal injection and inappropriate schedule of product administration have been considered as not related to the suspect vaccine, but to a human factor. This case is considered as non-serious.; Sender's Comments: A male patient was vaccinated with the first dose of Jynneos, at a dose reported as 0.1 ml, intradermally, for monkeypox prophylaxis, which is considered as intradermal injection. Reportedly, on the day 23 after the first dose, the patient was vaccinated with the second dose of Jynneos, at a dose reported as 0.1 ml, intradermally, which is considered as inappropriate schedule of vaccine administered and intradermal injection. At the time of this report, it was unknown if the patient experienced any adverse event due to Jynneos. Intradermal injection and inappropriate schedule of product administration are considered as listed per company convention. The patient's medical history and concomitant medication details were not reported. Intradermal injection and inappropriate schedule of product administration have been considered as not related to the suspect vaccine, but to a human factor. This case is considered as non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 18.11.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Wrong technique in product usage process
Symptomtext
This is the client's initial dose of the Jynneos vaccine series. Jynneos vaccine 0.1 ml given intradermally in the client's right forearm, but no wheal was visualized. Additional dose of Jynneos 0.1 ml given intradermally in the right arm 2 inches away from initial attempt and wheal was visualized.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 24.10.2022
- 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: ja
No adverse event
Symptomtext
Patient was 16 years old at the time of the vaccination and given ID Jynneos vaccine. Patient had no adverse effects/side effects. Parent informed SQ should have been given and will be given 4 weeks later at dose #2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 16.10.2022
- Impfdatum
- 16.10.2022
- Beginn
- 16.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Heart rate increased
Symptomtext
Client complained of fast heart rate post vaccination while waiting in the observation room. Vital signs initiated. Water, ice pack, candies provided and other care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate increased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 15.10.2022
- Impfdatum
- 11.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site swelling
Symptomtext
Bump at vaccination site in the forearm lasting more than 4 weeks. I still have the bump to this day.. Such a long side effect exceeds the expected duration of the bump that was communicated at the time of vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 14.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine exp. 10/7/2022 -(use by date) 8 weeks following - defrost VS Exp. date 10/31/2024
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 14.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine exp Use by date = 10/7/2022(8wks after defrost) Exp. Date = 10/31/2024
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 14.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine exp: use by date = 10/7/22 8 wk after defrost Exp Dae 10/31/2024
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- ACE inhibitors, Sulfamethoxazine - trime
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 14.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine exp. use by date = 10/7/22 8 weeks follow defrost VS Exp. date 10/31/2024
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 14.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine exp: use by date 10/7/2022 8 wk after defrost Exp Date 10/31/2024
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 14.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine exp. use by date = 10/7/22 8 weeks after defrost exp. date = 10/31/2024
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- bactrim
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 14.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine exp. use by date = 10/7/22 8weeks follow defrost VS. Exp. date 10/31/2024
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 45,0
- Geschlecht
- U
- Eingang
- 14.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine exp: use by date 10/7/22 8 weeks & defrost exp. date: 10/31/2024
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 14.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine exp. use by date 10/7/22 8 weeks and defrost exp. date: 10/31/2024
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 14.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine: Use by date = 10/17/2022 8 wk after defrost Exp. date = 10/31/2024
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- U
- Eingang
- 14.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine exp: Use by date = 10/7/22 8 wk after defrost Exp. Date = 10/31/2024
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Ciprofloxacin, dust, grass & wheat
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Client was mistakenly vaccinated with a vial of vaccine that had expired the day before. Medical director and manufacturer were contacted, and the recommendation is to revaccinate the client. Client was called and made aware of the issue, and he will call us back to make an appointment for his next dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 11.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syringe issue
Symptomtext
RN was administering Monkeypox Jynneos vaccine intradermally to client in L lower forearm and some of the vaccine leaked out. Then, RN readminisered Monkeypox Jynneos vaccine 2 inches away from original site successfully intradermally.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 10.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong technique in product usage process
Symptomtext
2nd dose administered due to no wheal formation on 1st attempt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 10.10.2022
- Impfdatum
- 04.10.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong technique in product usage process
Symptomtext
2ND Dose administered due to no wheal formation on 1st attempt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 24.09.2022
- Beginn
- 24.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Symptomtext
Jynneos vaccination error. pat5ent revaccinated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 21.09.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Symptomtext
Jynneos vaccination error. Patient revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 15.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Wrong technique in product usage process
Symptomtext
Jaynneos vaccination error. Patient trvaccinated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Symptomtext
Jaynneos vaccination error. Patient revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Symptomtext
Jaynneos vaccination error. Patient revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Wrong technique in product usage process
Symptomtext
Jaynneos vaccination error. Patient revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 49,0
- Geschlecht
- U
- Eingang
- 06.10.2022
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Symptomtext
Jaynneos vaccination error. Patient revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 03.10.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
First dose received 09/07/2022 and received 2nd dose 09/30/2022 (too early). No adverse events noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 30.09.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong technique in product usage process
Symptomtext
ID administration of 1st attempt - Wheal and observed leakage. Successful 2nd administration intradermally.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 30.09.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Syringe issue
Symptomtext
IM administration of 1st attempt - Wheal and observed leakage. Successful 2nd administration subcutaneously.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 29.09.2022
- Impfdatum
- 29.09.2022
- Beginn
- 29.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syringe issue
Wrong technique in product usage process
Symptomtext
RN, attempted intradermal placement of Jynneos Monkeypox vaccine with leakage from site on L forearm. A second attempt was made 2 inches higher from original site on L forearm and was successfully done intradermally. Pt. tolerated well and had no ill effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 27.09.2022
- Impfdatum
- 27.09.2022
- Beginn
- 27.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong technique in product usage process
Symptomtext
On first attempt at administering vaccine Intradermally, no wheal made. Wheal made on second attempt.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- None needed.
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- unknown
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 23.09.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong technique in product usage process
Symptomtext
No Wheal and observed leakage on first Intradermal administration attempt. Successful 2nd administration subcutaneously.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
No wheal the first time. Administered a second dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vaccination error
Symptomtext
Did not get a wheal the first time. A second dose was administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong technique in product usage process
Symptomtext
1st intradermal shot did not create a wheal. 2nd intradermal injection created wheal . Pt left in no distress from injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Therapeutic response changed
Symptomtext
First wheal was not created. Had to repeat ID injection. Pt left in No Distress.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Therapeutic response changed
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 20.09.2022
- Beginn
- 20.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
During first attempt of intradermal injection, a wheal was not visible. Per standing order guidelines, the nurse attempted the administration a second time in the opposite forearm. She was successful on the second attempt. The patient has not reported signs or symptoms of an adverse reaction following vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 20.09.2022
- Impfdatum
- 17.09.2022
- Beginn
- 17.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Heart rate increased
Symptomtext
Client complained of fast heart rate post vaccination . No other symptoms or chest pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate increased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No known illness.
- Vorgeschichte
- N/A.
- Andere Medikamente
- N/A. No medicaton or supplements taken at this tme.
- Allergien
- No known allergies.
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 17.09.2022
- Beginn
- 17.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient was given second dose one day too early. First dose given 8/25/2022 and second dose given 9/17/2022. Second dose given 23 days from first dose. Patient did not report any adverse effects during 15 minute wait period post vaccination. Patient was notified of early vaccination and did not report any adverse reactions and the time of call (9/17/2022 @17:48. When called pt stated , " I feel fine." Pt was given information to health department.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Pt. is immunocompromised per screening and consent form
- Vorgeschichte
- Pt. is immunocompromised per screening and consent form
- Andere Medikamente
- Unknown
- Allergien
- None listed
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Symptomtext
First wheal was not created. Had to repeat ID injection. Pt left in no distress
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong technique in product usage process
Symptomtext
First wheal was not created. Had to repeat ID injection. Pt left in NO Distress.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Symptomtext
First wheal was not created. Had to repeat ID injection. Pt left in no distress
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 15.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
First wheal was not created. Had to repeat ID injection. Pt left in NO Distress
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Symptomtext
First wheal was not created Had to repeat ID injection. Pt left in NO Distress
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 15.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Wrong technique in product usage process
Symptomtext
No Wheal and observed leakage on first Intradermal administration attempt. Successful 2nd administration intradermally
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 15.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect route of product administration
Product administered to patient of inappropriate age
Symptomtext
Dose administered intradermally instead of SQ (Patient is 17 years of age)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 14.09.2022
- Impfdatum
- 01.08.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram
Laboratory test
Peripheral swelling
Symptomtext
Swelling in bilateral feet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram
- Hospital-Tage
- -
- Labordaten
- EKG labs and a short course of lasix.
- Aktuelle Erkrankungen
- nonw
- Vorgeschichte
- Type 2 diabetes.
- Andere Medikamente
- albuterol, abilify, celexa, lasix, humalog, vascepa, lisinopril, melatonin, metformin, metolprolol, pravastatin, sildenafil, terbinafine, tresiba
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 14.09.2022
- Impfdatum
- 01.08.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 29,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram
Laboratory test
Peripheral swelling
Symptomtext
Swelling in bilateral feet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram
- Hospital-Tage
- -
- Labordaten
- EKG labs and a short course of lasix.
- Aktuelle Erkrankungen
- nonw
- Vorgeschichte
- Type 2 diabetes.
- Andere Medikamente
- albuterol, abilify, celexa, lasix, humalog, vascepa, lisinopril, melatonin, metformin, metolprolol, pravastatin, sildenafil, terbinafine, tresiba
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Symptomtext
1st intradermal shot did not create a wheal. 2nd intradermal injection created wheal. Pt left in no distress from injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Symptomtext
1st intradermal shot did not create a wheal. 2nd intradermal injection created wheal. Pt left in no distress from injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 13.09.2022
- Beginn
- 13.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vaccination error
Symptomtext
Missed wheal on first attempt, obtained successful wheal on second attempt.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Unknown.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 13.09.2022
- Beginn
- 13.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syringe issue
Symptomtext
attempt to vaccinate ID in LFA no wheal with full dose leakage. second attempt made 2 inches from first attempt in LFA. at least 1/2 vaccine leaked from ID attempt. SQ dose given in LA. Dose given successfully.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 11.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Vaccination error
Symptomtext
Jynneos vaccination error, no wheal. Administered 0.5 SQ given
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 11.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vaccination error
Symptomtext
Jnneosvaccination error, no wheal
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- . Patient revaccinated 0.5 SQ
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 09.09.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong technique in product usage process
Symptomtext
No Wheal and observed leakage on first Intradermal administration. 2nd administration was successful subcutaneously.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 09.09.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Needle issue
Symptomtext
On first attempt at ID vaccine administration needle appeared to be too superficial and once vaccinator pushed the plunger the vaccine leaked onto the client's arm. Dose successfully administered using ID method on 2nd attempt - 2 inches away from 1st attempt.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Needle issue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Swelling
Vaccination site bruising
Symptomtext
A red line extends along a lymphatic drainage pathway in the left arm of the patient, with a slightly raised profile, from the overall contusion formed from the vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Sertraline, 100mg Bupropion XL, 150mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyskinesia
Incorrect dose administered
Needle issue
Symptomtext
At the time of administering the vaccine ID the client suddenly moved - jerking his arm away. Vaccine was seen running down patients arm so full dose was not given. Successfully re- administered on same arm using sub-cut method.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyskinesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Wrong technique in product usage process
Symptomtext
Did not get a wheal and repeated dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none lisit
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Needle issue
Symptomtext
During 1st attempt at ID vaccine administration needle was not completely under the skin and a small amount of vaccine pooled on top of the skin. A successful 2nd ID vaccination was done 2 inches away from the 1st attempt on the same arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong technique in product usage process
Symptomtext
No Wheal on first Intradermal administration. 2nd administration was successful subcutaneously.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 06.09.2022
- Impfdatum
- 16.08.2022
- Beginn
- 26.08.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Cytomegalovirus test positive
Epstein-Barr virus test positive
HIV test negative
Immune thrombocytopenia
Immunoglobulin therapy
Platelet count abnormal
Symptomtext
Patient developed severe ITP and was hospitalized on 8/26/22 through 8/27/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cytomegalovirus test positive
- Hospital-Tage
- 2,0
- Labordaten
- platelet count improved with IVIG and dexamethasone EBV and CMV low positive HIV negative
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Flonase PRN
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 06.09.2022
- Impfdatum
- 06.09.2022
- Beginn
- 06.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vaccination error
Symptomtext
Intradermal route attempted by vaccinator. No wheal produced. vaccine the administered by subcutaneous route in other arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 06.09.2022
- Impfdatum
- 06.09.2022
- Beginn
- 06.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect route of product administration
Symptomtext
attempted to give vaccine via intradermal route - no weal noticed. gave vaccine subcutaneously.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 06.09.2022
- Impfdatum
- 06.09.2022
- Beginn
- 06.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect route of product administration
Symptomtext
attempted to inject smallpox vaccine via intradermal route - no weal noticed. Attempted second time, no weal. Vaccine give via subcutaneous route with 0.5ml dosage.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- -
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 05.09.2022
- Impfdatum
- 04.09.2022
- Beginn
- 05.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Erythema
Swelling
Symptomtext
Redness and swelling about the size of a quarter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 03.09.2022
- Impfdatum
- 03.09.2022
- Beginn
- 03.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Wrong technique in product usage process
Symptomtext
Client's intradermal Jynneos-BN 0.1mL injected into Left Forearm at 5 degrees did not produce a wheal or bleb, client informed that this was not expected result and would need another injection, he verbalized understanding and 0.5mL Jynneos-BN given subcutaneously in the back of the left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Denies having any allergies
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 01.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administration error
Symptomtext
First attempt of jynneos vaccine given in Left forearm with no elevation of the skin or wheal present after administering. Second dose attempt of jynneos in left forearm with a wheal formed by another nurse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administration error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 21,0
- Geschlecht
- U
- Eingang
- 01.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong technique in product usage process
Symptomtext
No Wheal on first Intradermal administration. Successful wheal on 2nd ID attempt.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 31.08.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong technique in product usage process
Symptomtext
No Wheal on first or 2nd Intradermal administration. Full Dose given Subcutaneously.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 31.08.2022
- Impfdatum
- 25.08.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
Vaccine #2 given at 21 days. Patient had no complications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 31.08.2022
- Impfdatum
- 25.08.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
Vaccine was given at 21 days. Patient had no complications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 31.08.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect route of product administration
Symptomtext
No Wheal on first administration. 2nd administration was successful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 31.08.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong technique in product usage process
Symptomtext
No Wheal on first administration. 2nd administration was successful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 31.08.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administration error
Symptomtext
No Wheal on first administration. 2nd administration was successful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administration error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 30.08.2022
- Impfdatum
- 30.08.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
PT RECEIEVED SECOND DOSE OF VACCINE 3 DAYS TOO EARLY. 1ST DOSE GIVEN WAS ON 8/9/22. PT DID NOT HAVE ANY ADVERSE REACTIONS BUT DID RECEIVE THE VACCINE TOO EARLY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NOT AWARE
- Vorgeschichte
- NOT AWARE
- Andere Medikamente
- Not aware
- Allergien
- BEE STING NOTED ON CONSENT FORM
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 29.08.2022
- Impfdatum
- 29.08.2022
- Beginn
- 29.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Wrong technique in product usage process
Symptomtext
Patient came to clinic for first dose of Monkeypox vaccine. The patient moved her arm during the intradermal dose administration, the wheel was not achieved. The patient requested a subcutaneous dose. Subcutaneous dose administered without incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- unknown
- Allergien
- reports allergy to Norco - hives
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 29.08.2022
- Impfdatum
- 29.08.2022
- Beginn
- 29.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Circumstance or information capable of leading to medication error
Symptomtext
Attempted ID administration of vaccine, did not achieve wheal on left arm. Tried again with fresh dose and needle, achieved wheal on right forearm. No injury to patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Unknown.
- Andere Medikamente
- Unknown.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 27.08.2022
- Impfdatum
- 27.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination error
Symptomtext
Patient was asked all pre-screening questions, no contra-indication. he was vaccinated with 0.1ml of jynneos/BN, wheal was not pbtain on first try, patient was vaccinated a second time 2 inches away from initial site a wheal was obtain. ( this is a second report , unsure if first report went through)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 27.08.2022
- Impfdatum
- 27.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong technique in product usage process
Symptomtext
Patient asked all pre-screening questions, no contra-indications, he was vaccinated with .1ml of Jynneos intradermal on left forearm, wheal was not obtain on first try. Pt was vaccinated a second 2-inches away from initial site time wheal obtain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong technique in product usage process
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 27.08.2022
- Impfdatum
- 27.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Syringe issue
Underdose
Symptomtext
Patient was asked pre-screening questions, no contra-indications to vaccine. while vaccinating patient, needle got disconnected from syringe causing most of the vaccine to leak out. Patient was vaccinated with a new dose vaccine, 2-inches away from the site, team lead was made aware. Patient did not c/o of any discomfort.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 25.08.2022
- Impfdatum
- 23.08.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- ID / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Skin warm
Symptomtext
Cellulitis 5" x 3" Skin hot to touch. Placed on antibiotics as a precaution.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vyvanse, Dscovy
- Allergien
- Ceclor
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 19.08.2022
- Impfdatum
- 16.08.2022
- Beginn
- 16.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product use issue
Symptomtext
Client was not eligible for vaccination and should not have received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product use issue
- Hospital-Tage
- -
- Labordaten
- Client tested positive for Monkey Pox virus on 08/01/2022. This results was available in client's record.
- Aktuelle Erkrankungen
- Positive for Monkey Pox
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 16.08.2022
- Beginn
- 16.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient received vaccination 7 days prior to the scheduled dosing date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 10.08.2022
- Impfdatum
- 10.08.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient received second dose of Jynneos vaccine too soon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -