- Staat
- MD
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Presyncope
Symptomtext
Vasovagal bout 10 seconds and lied on exam bed. No injury and was oriented.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- n
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 01.09.2021
- Impfdatum
- 31.08.2021
- Beginn
- 31.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Electrolyte substitution therapy
Hyperhidrosis
Loss of consciousness
Nausea
Pallor
Vomiting
Symptomtext
Approximately 15-20 minutes after tetanus shot. Donor stated that she was not feeling well prior to tetanus shot, but did not disclose this to staff or report this to MSA before tetanus shot was administered. Donor experienced lightheadedness/dizziness, nausea/vomiting, and was pale and sweaty. Donor sat on the floor to prevent a fall due to dizziness. Donor stated she was not feeling well prior to vaccine and that she has been having similar reactions to donating recently donor disclosed that after a previous donation she passed out at home. Donor provided 12 oz of oral electrolyte fluids
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Hydroxyzine Lexapro Loestrin Vitamin D
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 10.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blindness
Dizziness
Feeling hot
Loss of consciousness
Symptomtext
Patient felt dizzy, hot, and described his vision as "everything went black." Patient passed out but was caught by his mother and lowered to the floor. He was given cool washcloths, BP monitored, pulse ox and pulse monitored. First vitals: BP 104/63, pulse 72, POx 99; Second vitals: BP 108/72, Pulse 103 (moved to a sitting position), POx 99; Third vitals 117/76, Pulse 77, POx 99; BP 120/74 (standing), Pulse 88, POx 98. Patient reported last eating a meal at noon. Patient was given water and a Coca-Cola to drink.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 01.04.2021
- Impfdatum
- 01.04.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyskinesia
Eye movement disorder
Loss of consciousness
Pallor
Symptomtext
4/1/2021 1135 - Administered Menactra and Tdap in client's right deltoid in that order. About 10 seconds after receiving Tdap, client's eyes rolled back in head, skin paled, and client lost consciousness. RN and mother supported client upright in chair. Client had 5 involuntary muscle spasms of upper torso. 30 seconds after losing consciousness, client regained consciousness without intervention. Nurse and mother assisted client into recovery position on the floor. Another nurse retrieved cold washrag, cold water, and graham crackers. Cold washrag applied to back of the neck. After 2 minutes on the floor, client's color returned and client stated feeling better. Nurse administered HPV into left deltoid with client in side-lying position on floor, no reaction. Mother stated client had never had a syncopal episode with vaccinations before, but has another child prone to syncopal episodes. When asked if client had breakfast, both client and mother said no. About 5 minutes after receiving HPV vaccine, client felt well enough to move into a sitting position, tolerated graham crackers and water. After 5 minutes in sitting position, client felt able to stand. Client stood for 2 minutes and stated feeling fine. Client escorted by mother out of clinic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Denies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 08.06.2021
- Impfdatum
- 06.06.2021
- Beginn
- 06.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injected limb mobility decreased
Injection site erythema
Injection site hypoaesthesia
Injection site induration
Injection site paraesthesia
Injection site swelling
Pain in extremity
Peripheral coldness
Symptomtext
Reports began to experience pain in left arm approx. 2 hours after receiving the tetanus immunization. States later in the day 6/6/21 began to have a line of swelling from his immunization site to his elbow/ac area that was reddened and hard and cold to touch. Denies increased warmth. States pain continues and includes numbness, tingling and shooting pains in left arm. Reports that due to swelling and pain is unable to lift or extend left arm. Denies any other symptoms including any breathing problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Denies
- Vorgeschichte
- Denies
- Andere Medikamente
- Ibuprofen prn for aches and pains
- Allergien
- Denies allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 23.05.2021
- Impfdatum
- 22.05.2021
- Beginn
- 22.05.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bone pain
Chest pain
Pain
Pain in extremity
Symptomtext
SEVERE RIGHT COLLARBONE PAIN RADIATING TO CHEST AND BOTH ARMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- NEXPLANON FOR BIRTH CONTROL TO L UPPER ARM
- Allergien
- LATEX
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 17.05.2021
- Impfdatum
- 12.05.2021
- Beginn
- 15.05.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Hypoaesthesia
Injection site erythema
Injection site pain
Injection site swelling
Injection site warmth
Pain in extremity
Paraesthesia
Peripheral swelling
Symptomtext
May 12th pt. received the TDAP vaccine. Patient reports - first two days lt. arm was only a little sore but nothing else happened. By 05/15/21 , pt. noticed swelling, redness and more pain. Currently, patient reports lt. arm is aching much more (a kind of pain that goes from the vaccination site to the elbow), reports pain 5/10 on a 1:10 pain scale ratio; swelling, redness, warmth to injection site, fingers are feeling tingly. Patient reports using ice intermittingly. RN suggested warm/ cold compress, use of Ibuprofen for swelling and pain, and to seek medical attention for increasing concerns or if numbness continues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 10.03.2021
- Impfdatum
- 08.03.2021
- Beginn
- 09.03.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Decreased appetite
Fatigue
Feeling cold
Feeling hot
Hyperhidrosis
Mobility decreased
Pyrexia
Symptomtext
Donor reports that when he awoke at approx. 0500 on 3/9/21 he was feeling feverish with chills and too tired and weak to get out of bed. Reports remained bedridden throughout the day and into the early am of 3/10/2021. Reports decreased appetite and that he continued to feel feverish with alternating periods of cold and hot with sweating. Unable to take his own temperature. Denies N/V, diarrhea, headache, dizziness, LOC; also denies any rashes to body or dyspnea. Denies any swelling, redness, pain/numbness/tingling to right arm/hand. At approx. 0930 on 3/10/2021 donor reported feeling much better and believed the fever had broken. Was tolerating fluids well and able to get up and about independently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Allergy to abilify; no other allergies.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 07.02.2021
- Impfdatum
- 30.12.2020
- Beginn
- 08.01.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Bacterial test negative
CSF pressure increased
CSF white blood cell count increased
Dehydration
Headache
Magnetic resonance imaging head abnormal
Magnetic resonance imaging spinal abnormal
Myelitis
Pyrexia
Urinary retention
Symptomtext
Developed fever and headache on 1/8/21. Patient with intermittent fevers and persistent headache. Seen by PCP. Admitted to Facility from 1/21-1/22 for headache and dehydration; symptoms improved with IVF. Increasing headache and complaint of urinary retention then occurred -- readmitted to Facility on 1/25/21. Work-up consistent with myelitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- 6,0
- Labordaten
- 1/26/21 Brain and spine MRI = lesions of the central spinal gray matter, bilateral thalami, and periaqueductal gray matter. 1/26/21 LP = elevated open pressure; elevated WBC in spinal fluid with negative bacterial culture.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 24.03.2021
- Beginn
- 26.03.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Contusion
Rash erythematous
Urticaria
Symptomtext
Narrative: 32 yo female received a Tdap vaccine in March 2021. A few days later, she secure-messaged her primary care team stating that for the past 5 days, she had red spots/bruising throughout her body she believed to be hives. She stated that she takes daily Zyrtec and started taking OTC Benadryl to help with the symptoms. She also stated that she gets hives from the influenza vaccine. She had a video Appointment with her PCP who suggested she sees an allergist prior to any other vaccinations such as the Covid vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 19.07.2021
- Impfdatum
- 09.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site warmth
Pain
Pyrexia
Symptomtext
1 day after receiving vaccine, fever and body aches. 6 days after-injection site redness and hot to touch, up shoulder and down to elbow, continued to have fever and body aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Chlamydia Tx
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 13.07.2021
- Impfdatum
- 21.05.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 53,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Symptomtext
Donor stated that he had persistent soreness to his left arm at the puncture site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- Donor stated that he might have had tetanus at the time of her immunization because he cut his hand and did not have it evaluated.
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Tetanus
- Staat
- UT
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 22.04.2021
- Impfdatum
- 16.04.2021
- Beginn
- 16.04.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site induration
Injection site pain
Injection site swelling
Injection site warmth
Symptomtext
REDNESS, SWELLING, HEAT, PAIN STARTED 2 HOURS AFTER SHOT ON 4/16/21..PATIENT SAID IT WAS ABOUT A 6 INCH AREA. WHEN SHE CAME INTO CENTER ON 4/21/21 THE AREA WAS 2 INCHES AROUND INJECTION SITE, RED, WARM, TENDER AND HAS A NICKLE SIZED HARDENED AREA AT INJECTION SITE. DONOR DENIES ANY OTHER SYMPTOMS, HAS NOT BEEN FEBRILE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- ACNE, ASTHMA
- Andere Medikamente
- COVID VACCINE COMPLETED (MODERNA), BIRTH CONTROL, CLINDAMYCIN CREAM, TRIANCINOLONE CREAM, ALBUTEROL HHN, FAMOTIDINE, PANTOPROZOLE, PROTONIX, BUPROPRION
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 18.04.2021
- Impfdatum
- 13.04.2021
- Beginn
- 14.04.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nodule
Pain in extremity
Pruritus
Skin warm
Symptomtext
On 04/13/2021, the patient donated plasma at CSL plasma and received a free Tetanus vaccination. The patient did not experience any symptoms until the day after immunization. The patient describes soreness, itchiness, warmth, and nodule formation in the right arm deltoid region. Patient denies difficulty breathing or chest pain. Nodule formation was initially the size of a dollar coin but has reduced to the size of a dime during examination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Not applicable
- Vorgeschichte
- Mental health issues
- Andere Medikamente
- protonix , magnesium , carbamazepine , Zoloft , clonidine,
- Allergien
- erythromycin, Sulfa, Betadine, shellfish, Codeine, Morphine
- Vorherige Impfungen
- Patient states that the pneumonia vaccination in October 2016 caused lymph node swelling.
- Staat
- OK
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 05.04.2021
- Impfdatum
- 19.03.2021
- Beginn
- 21.03.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Injection site erythema
Injection site warmth
Myalgia
Nausea
Pain
Symptomtext
Redness, nausea, headache, muscle ache, fatigue, warmth to vaccine site and hurt to lift arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- hypetension
- Andere Medikamente
- Atenolol, verapamil and aspirin
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 01.04.2021
- Impfdatum
- 26.03.2021
- Beginn
- 28.03.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site induration
Injection site pain
Pruritus
Rash
Symptomtext
Patient reports two days after Tetanus shot that left arm is tender along with hardening at injection site. Patient also states rash noted on back of neck: describes rash as two lines with itching at local site around neck. Patient denies any shortness of breath and was advised to monitor rash area and notify facility if symptoms and/or condition worsens. Outcome: Patient reported on follow up call on 04/01/2021 that rash and tenderness had subsided, injection site hardening remains.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site induration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None listed
- Vorgeschichte
- None Listed
- Andere Medikamente
- None listed
- Allergien
- None listed
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 09.02.2021
- Impfdatum
- 04.02.2021
- Beginn
- 08.02.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Diarrhoea
Nausea
Rash
Symptomtext
Abdominal pain, nausea, and diarrhea and rash. No fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 13.01.2021
- Impfdatum
- 19.11.2020
- Beginn
- 29.11.2020
- Tage bis Beginn
- 10,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pain in extremity
Symptomtext
Left arm/shoulder pain persisting beyond 11 days after the vaccine was given Concern for SIRVA despite the clinician recalling the location of the injection as being properly placed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- penicillin: hives
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 08.01.2021
- Impfdatum
- 04.01.2021
- Beginn
- 05.01.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Severe swelling, redness, and pain at the injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 07.01.2021
- Impfdatum
- 30.11.2020
- Beginn
- 02.12.2020
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Symptomtext
Worsening shoulder pain over 1 month later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Cervical Radiculopathy, Anxiety, Episodic Headaches.
- Andere Medikamente
- Vitamin D, Lexapro 10mg.
- Allergien
- Medrol, Prednisone.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 05.01.2021
- Impfdatum
- 30.12.2020
- Beginn
- 30.12.2020
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash pruritic
Symptomtext
Patient is a 11y.o. female who complains of rash. She got Tdap, menactra 12/30. That night started with little rash on forehead. Itchy and spread across face. 12/31 very itchy, spreading down neck. Used some hct. Examined 1/4/2021. Rash does not come and go. Remains on face. Now nose, eyelids, ears, chin. Some bumps on arms. Did not eat today, but feeling fine. No runny nose or cough, no sore throat, no abdominal pain or diarrhea. Sleeping fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash pruritic
- Hospital-Tage
- -
- Labordaten
- Telemedicine visit and exam 1/4/2021
- Aktuelle Erkrankungen
- none reported per patient
- Vorgeschichte
- Eczema, cholesteatoma (corrected)
- Andere Medikamente
- Zyrtec 5mg tabs, 1 tab by mouth as needed
- Allergien
- seasonal, no known medication allergies
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
a patient inadvertently received ADACEL instead of DTAP with no reported adverse event; Initial information received on 24-Jan-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 1 years old female patient who inadvertently received Adacel instead of DTAP with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included INFLUENZA VACCINE (FLUZONE [INFLUENZA VACCINE]) for Immunization; and PNEUMOCOCCAL VACCINE (PNEUMOCOCCAL VACCINE) for Immunization. On 07-Dec-2021, the patient received a dose of 0.5 ml of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE (formulation, strength: unknown) lot U6830AA via intramuscular route in the left thigh as Immunisation. On 07-DEC-2021 the patient developed a non-serious event "a patient inadvertently received Adacel instead of DTAP with no reported adverse event" (wrong product administered) same day following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE.. It was reported" Caller reporting the nurse who administered the vaccine was unsure of which patient received the ADACEL, it was between two patients. Caller reporting the nurse was falsifying records, she had a pocket full of vials at the end of the day and had to sort out who received what vaccination." Action taken with DIPHTHERIA, TETANUS AND ACELLULAR PERTUSSIS VACCINE (ADACEL) was not applicable. It was not reported if the patient received a corrective treatment for the event (a patient inadvertently received ADACEL instead of DTAP with no reported adverse event). At time of reporting, the outcome was Unknown for the event a patient inadvertently received Adacel instead of DTAP with no reported adverse event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
a patient inadvertently received ADACEL instead of DTAP with no ae; Initial information received on 24-Jan-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 1 years old female patient who experienced a patient inadvertently received adacel instead of dtap with no adverse event while receiving vaccine DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included HIB VACCINE (HIB); and PNEUMOCOCCAL VACCINE (PNEUMOCOCCAL VACCINE). On 07-Dec-2021, the patient received a dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE lot U6830AA via (unknown route, strength) (expiry date:17-Sep-2022) in unknown administration site for prophylactic vaccination. On 07-DEC-2021 the patient developed a non-serious event "a patient inadvertently received adacel instead of dtap with no adverse event " (wrong product administered) following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. It was reported"the nurse who administered the vaccine was unsure of which patient received the ADACEL instead of DTAP, it was one of the reported two patients. Caller reporting the nurse was falsifying records, she had a pocket full of vials at the end of the day and had to sort out who received what vaccination. See related case on second patient #00946669". Action taken with DIPHTHERIA, TETANUS AND ACELLULAR PERTUSSIS VACCINE (ADACEL) was not applicable. It was not reported if the patient received a corrective treatment for the event (a patient inadvertently received ADACEL instead of DTAP with no ae). At time of reporting, the outcome was Unknown for the event a patient inadvertently received adacel instead of dtap with no ae. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the guidelines. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 1,5
- Geschlecht
- U
- Eingang
- 04.01.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
gave Adacel to an 18 month old with no adverse event; Initial information received on 29-Dec-2020 regarding an unsolicited valid non-serious case from a nurse. This case involves a 18 month old patient who was administered diphtheria-2/tetanus/5 ac pertussis vaccine (Adacel) by mistake (product use issue) (batch number: U6830AA and expiration date: unknown) 4th dose via unknown route in unknown administration site for prophylactic vaccination. The patient's medical history, medical treatment(s), vaccination(s), family history and concomitant medications were not provided. This was an actual medication error case due to the event product use issue (latency: unknown). At the time of reporting, no adverse event was reported. No laboratory data was reported. Disclaimer: This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in directive 2001/83/ec and module VI of the good Pharmacovigilance practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -