- Staat
- GA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 23.01.2023
- Beginn
- 23.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
5 MIN AFTER VACCINES WAS ADMINISTERED, PT PASSED OUT. AFTER ABOUT 30 SECONDS AFTER USING AMONIA UNDER NOSE. PT CAME ABOUT. PT WAS GIVEN 12OZ DR PEPPER. VS 90/60 L ARM PULSE 71 AND O2 SAT 98%. pT SAT UP FOR ABOUT 15 MIN BEFORE LEAVING CLINIC. PT HAD NOT EATEN BEFORE GETTING VACCINES. pT WAS ESCORTED TO CAR BY MYSELF AND MOTHER. WAS GOING TO GET SOMETHING TO EAT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Amoxil
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 13.01.2023
- Beginn
- 13.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
A couple of minutes after receiving all four vaccines, client stood and then half fainted into the arms of the nurse. She was immediately place in recliner chair and given juice and crackers as it was discovered she hadn't eaten anything today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Syncope
Symptomtext
Patient became nauseous and dizzy after immunization. Patient exhibited signs of fainting, however did not lose consciousness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 19.09.2022
- Impfdatum
- 19.09.2022
- Beginn
- 19.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Clonus
Dizziness
Dry skin
Eye movement disorder
Feeling of body temperature change
Head injury
Hyperhidrosis
Loss of consciousness
Pallor
Swelling
Tremor
Symptomtext
Following injections, child's arm became clonic and eyes rolled back, put child on the floor with legs elevated, diaphoretic. Child jumped up and stated does this, passes out. Sat child down on the bench and he became clonic again with arms and stared ahead. Eased child back down to the floor and the back of the childs head hit the floor. Resulted in a small elevated area on the posterior head. Vitals at 9:24AM were blood pressure left arm 120/40,Pulse 80, Respirations, child warm to touch, diaphoretic, face pale. Elevated legs, ice pack on the back of the head and cold compress on forehead. 9:35AM Vitals blood pressure 102/50, Pulse 78, Resp. 24, c/o being hot then cold. sat up the child and become lightheaded so layed back down at 9:40AM, Lips pale. 9:50AM blood pressure 94/30 pulse 72, Respirations 10 States not lightheaded, skin dry to touch and not hot. States feels better so was sitting and then would lay down in front of a fan. 10:01AM, blood pressure 120/72, Pulse 80, Resp. 12, states feeling better, lips red, skin warm to touch sitting up. Tried standing up and stated weak and sat back down on the bench. 10:04 AM blood pressure 120/70, Pulse 82, Resp 12, While sitting observed involuntary shaking of legs and arms. Child stated feeling better. at 10:15AM walked child to vehicle. Recommended to the adult with child that the child should rest the rest of this day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- I asked and none reported other than child stated he faints very easily.
- Andere Medikamente
- Unknown
- Allergien
- NkA
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 24.08.2022
- Beginn
- 24.08.2022
- 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
patient had a vaso-vagel episode /vital signs checked/ po fluids given/patient discharged to home after approx 30 minutes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 19.08.2022
- Impfdatum
- 19.08.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Dreamy state
Syncope
Symptomtext
11:07, Right after administering HPV patient had an episode of syncope that lasted approx. 5 seconds. Pt states he felt as he was dreaming. Patient oriented X3 and was given cookies, juice, and candy. 11:29 states he felt fine and no longer felt faint.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Asthenia
Eye pruritus
Headache
Lip swelling
Pruritus
Tremor
Symptomtext
Within 15 minutes of patient receiving the above four vaccines (HPV, Covid bivalent booster, MCV, and TDaP), the patient developed lip swelling, subjective weakness, headache, abdominal pain, and felt "shaky." She briefly felt itchy over the right calf muscle and around the eyes. No hives. Vital signs normal - no hypotension. No wheezing or throat swelling. She received Benadryl and ibuprofen and symptoms resolved within one hour.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Constipation, dandruff, eczema
- Vorgeschichte
- Bilateral femoral anteversion
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 23.08.2022
- Impfdatum
- 15.08.2022
- Beginn
- 16.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injected limb mobility decreased
Injection site pain
Pain in extremity
Peripheral swelling
Skin tightness
Tenderness
Symptomtext
first L. upper arm was sore but as the week has progressed. the pain has spread all the way down to her hand. Her forearm feels swollen and tight. No redness or warmth but the entire arm is very tender. Can barely lift her arm from her side
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 14.07.2023
- Impfdatum
- 14.07.2023
- Beginn
- 14.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Vomiting
Symptomtext
At 10:30am on 7/14/2023The nurse administered TDaP (Adacel) into right deltoid and then HPV (Gardasil 9) IM into Left Deltoid. Immediately after administration, patient started to vomit The. Nurse Practitioner and Doctor were notified and patient was evaluated by the providers. Patient blood pressure was checked and patient was given water and instructed to lie down on table. Patient stayed in office for extra 15 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No know food or drug allergies
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 09.01.2023
- Impfdatum
- 09.01.2023
- Beginn
- 09.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Dyspepsia
Headache
Vertigo
Symptomtext
Approximately 6 minutes after receiving the above vaccines, the patient was very apprehensive, and began to complain of vertigo, heartburn & temporal-area headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None.
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 22.08.2022
- Beginn
- 23.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Crying
Electromyogram
Insomnia
Joint range of motion decreased
Pain
Product administered at inappropriate site
Shoulder injury related to vaccine administration
Symptomtext
I received a tetanus vaccine in the ED due to a minor cut on my finger. Within 2 days, the following occured Extreme shoulder pain, extreme limitation for range of motion; could not raise arm/elbow to about 1/3 of normal range. Aching/sharp pains. Pain made worse w/abduction motions. Pain often interferes w/sleep. Given Prednisone, 12 day course After round of prednisone was complete; pain, stiffness, and lack of mobility recurred. Dates of Treatment: 08/30/22 - Orthopaedics -> Initial Visit 09/19/22 - Orthopaedics -> Return for continued pain 09/23/22 - Neurology as recommended for possible nerve damage 09/27/22, 10/17/22, 11/10/22 - Physical Therapy Appointments 10/18/22 - Neurology Procedure - EMG testing On the evening of 8/21/22 I was in the ED for approx. 4 hours to receive 2 stitches from a laceration. The dept. was extremely busy and understaffed (I believe 1 doctor, 1 nurse and a few medical assistants). I was told that another Hospital that evening was better staffed and had a far less wait time. After being treated for the laceration, I was given a tetanus shot. The shot was not given in the deltoid muscle, but at the upper part of the shoulder, was told at my first appointment that I most likely had SIRVA and that the injection seemed to have been given in my bursa. I have received PT and have continued PT home exercises. Pain continues in the morning, improves as day goes on. Lack of sleep for the past 4 months, and during sleep I have been told I cry out in pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- 10/18/22 - EMG Testing
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 06.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Induration
Pain
Skin warm
Swelling
Symptomtext
warm, redness, swelling, large induration area, pain 4/10
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- Lexapro, losartan, folic acid, thiamine
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 19.08.2022
- Beginn
- 20.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pruritus
Injection site urticaria
Pain in extremity
Symptomtext
Itching and hives to right upper arm around injection site. Reports soreness to right arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No illness at time of vaccination or one month prior
- Vorgeschichte
- Asthma, Glaucoma to left eye
- Andere Medikamente
- Vitamin C, Zinc, Tumeric, Vitamin D3, Biotin, Probiotic, ProAir Inhaler PRN, Unknown Glaucoma eye drops
- Allergien
- Tramadol
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 18.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Pyrexia
Symptomtext
Felt feverish and had chills for one day. Now resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Anemia, Migraine without aura, History of ovarian teratoma (surgically removed)
- Andere Medikamente
- Mono-Linyah
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 15.11.2023
- Impfdatum
- 31.10.2023
- Beginn
- 31.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Tdap/adacel was indivertibly given to a child of 2 years old. No adverse reactions. Follow up made two days and seven days after administered. Parents reported no side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- n/a
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 26.05.2023
- Impfdatum
- 26.05.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Tdap was administered instead of DTAP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- n/A
- Vorgeschichte
- n/A
- Andere Medikamente
- Multivitamin Promethazine gel PRN Tylenol PRN Zyrtec
- Allergien
- PCN, Amoxicillin
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 27.04.2023
- Impfdatum
- 27.04.2023
- Beginn
- 27.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Hyperhidrosis
Pallor
Symptomtext
after last vaccine a few seconds later pt coughed and turned pale and sweaty. pt was laid back flat on the table. cool compress applied. water given 10 min later. pt sat in chair for 15 minutes then returned to class.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 27.10.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 4,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint swelling
Symptomtext
ankle swelling; Initial information received on 07-Nov-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 23 years old female patient who experienced ankle swelling after 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. On 27-Oct-2022, the patient received dose 0.5 ml Once (1x) (total) Diphtheria-2/tetanus/5 AC pertussis vaccine suspension for injection with strength: Unknown (lot- U7461AA, expiry date- 12-JUL-2024) via intramuscular route in the right deltoid for immunization. On 31-OCT-2022 the patient developed ankle swelling (joint swelling) latency: 4 days following the administration of Diphtheria-2/tetanus/5 ac pertussis vaccine. Action taken: not applicable. It was not reported if the patient received a corrective treatment for the event (ankle swelling). Outcome : Not Recovered / Not Resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Joint swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 15.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Expired product administered
Product use issue
Symptomtext
Mild Asthma; 3 patients received Pfizer covid 19 vaccine orange cap past the expiration date.; Additional Vaccines Administered on Same Date of the Pfizer Suspect: T-DAP -Sanofi, HPV - Merck, Influenza -Sanofi; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team, Program ID. An 11-year-old female patient received BNT162b2 (BNT162B2), on 05Oct2022 at 16:30 as dose 1 (orange cap), 0.2 ml single (Lot number: FL8095, Expiration Date: 31Aug2022) at the age of 11 years intramuscular, in left deltoid for covid-19 immunisation; influenza vaccine (INFLUENZA), on 05Oct2022 as dose 7, single (Lot number: UT7701KA, Expiration Date: 30Jun2023) intramuscular, in right deltoid for immunisation; hpv vaccine (HPV VACCINE), on 05Oct2022 as dose 1, single (Lot number: 1780878, Expiration Date: 02Dec2023) intramuscular, in right deltoid for immunisation; diphtheria vaccine toxoid, pertussis vaccine acellular, tetanus vaccine toxoid (TDAP), on 05Oct2022 as dose 1, single (Lot number: U7461AA, Expiration Date: 12Jul2024) intramuscular, in left deltoid for immunisation. The patient's relevant medical history included: "Allergy" (unspecified if ongoing), notes: She takes allergy meds but that was about it. The patient took concomitant medications. Vaccination history included: Influenza vaccine (Dose Number: 01, Sanofi), for Immunization; Influenza vaccine (Dose Number: 02, Sanofi), for Immunization; Influenza vaccine (Dose Number: 03, Sanofi), for Immunization; Influenza vaccine (Dose Number: 04, Sanofi), for Immunization; Influenza vaccine (Dose Number: 05, Sanofi), for Immunization; Influenza vaccine (Dose Number: 06, Sanofi), for Immunization. The following information was reported: EXPIRED PRODUCT ADMINISTERED (non-serious) with onset 05Oct2022 at 16:30, outcome "unknown", described as "3 patients received Pfizer covid 19 vaccine orange cap past the expiration date."; PRODUCT USE ISSUE (non-serious) with onset 05Oct2022 at 16:30, outcome "unknown", described as "Additional Vaccines Administered on Same Date of the Pfizer Suspect: T-DAP -Sanofi, HPV - Merck, Influenza -Sanofi"; ASTHMA (non-serious), outcome "unknown", described as "Mild Asthma". Therapeutic measures were not taken as a result of asthma. Additional information: The patient did not administer any other vaccinations within four weeks prior to the first administration date of the suspect vaccine and no AE(s) following prior vaccinations. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201223008 same reporter/drug/event, different patient;US-PFIZER INC-202201223295 same reporter/drug/event, different patient;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthma
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy (She takes allergy meds but that was about it)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 17.09.2022
- Impfdatum
- 30.08.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exposure during pregnancy
No adverse event
Product storage error
Symptomtext
t a low of negative 5.1C out of range for 12 minutes and a low of 1.3C out of range for 10 minutes. with no adverse event; poor quality product administered; currently pregnant with 3rd child taking Adacel with no reported adverse event; Initial information received on 06-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case is linked to cases 2022SA373167, 2022SA372581 and 2022SA372123. This case involves a 33 years old female patient who was exposed to vaccine DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] in context of currently pregnant with 3rd child taking adacel with no reported adverse event, poor quality product administered and t a low of negative 5.1c out of range for 12 minutes and a low of 1.3c out of range for 10 minutes. with no adverse event. Data regarding this pregnancy were received prospectively, i.e. before pregnancy outcome was known. The reported currently pregnant with 3rd child taking Adacel with no reported adverse event, poor quality product administered and t a low of negative 5.1C out of range for 12 minutes and a low of 1.3C out of range for 10 minutes. with no adverse event occurred at unknown gestation period. The date of last menstrual period was not reported. The estimated due date is 11-Oct-2022. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 30-Aug-2022, the patient received a dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE once (lot U7461AA; expiry date: 12-Jul-2024) via intramuscular route in the right arm for immunization. On 30-AUG-2022 the patient developed a non-serious currently pregnant with 3rd child taking adacel with no reported adverse event (exposure during pregnancy), poor quality product administered and to a low of negative 5.1c out of range for 12 minutes and a low of 1.3c out of range for 10 minutes. with no adverse event (product storage error) following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event currently pregnant with 3rd child taking adacel with no reported adverse event, was Unknown for the event poor quality product administered and was Unknown for the event t a low of negative 5.1c out of range for 12 minutes and a low of 1.3c out of range for 10 minutes. with no adverse event. Additionally, at time of reporting, the outcome of the pregnancy is unknown. Outcome of the pregnancy was reported as Birth Type unknown and fetal outcome was reported as Outcome unknown. 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.; Sender's Comments: 01266747: 01266903: 01266768: 01266921: 01266924: 01266780: 01266792: 01266974: 01266976: 01266978: 01266980: 01266982: 01266983: 01266985: US-SA-2022SA372080:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure during pregnancy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 30.08.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Poor quality product administered
Product storage error
Symptomtext
ADACEL at a low of negative 5.1C out of range for 12 minutes and a low of 1.3C out of range for 10 minutes and was administrated post excursion with no reported adverse event; ADACEL at a low of negative 5.1C out of range for 12 minutes and a low of 1.3C out of range for 10 minutes and was administrated post excursion with no reported adverse event; Initial information received on 06-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case is linked to cases 2022SA370866(CLUSTER), 2022SA372086(CLUSTER), 2022SA372581(CLUSTER), 2022SA372080(CLUSTER), 2022SA372584(CLUSTER), 2022SA373534(CLUSTER), 2022SA371564(CLUSTER), 2022SA371948(CLUSTER), 2022SA372095(CLUSTER), 2022SA372123(CLUSTER), 2022SA372180(CLUSTER), 2022SA371333(CLUSTER), 2022SA372199(CLUSTER), 2022SA373167(CLUSTER) and 2022SA373167(CLUSTER). This case involves a 79 years old female patient who was administrated DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] post excursion at a low of negative 5.1 C (Celsius) out of range for 12 minutes and a low of 1.3C out of range for 10 minutes and with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 30-Aug-2022, the patient received 0.5 ml, total dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE, unknown formulation (lot U7461A, exp date: 12-Jul-2024) via intramuscular route in the left arm as Immunization. On an unknown date the DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE at a low of negative 5.1C out of range for 12 minutes and a low of 1.3C out of range for 10 minutes (product storage error) and was administrated post excursion on 30-Aug-2022 with no reported adverse event (poor quality product administered) (latency: same day. Action taken: not applicable. At time of reporting, the outcome was Unknown for the events. 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.; Sender's Comments: US-SA-2022SA372080:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 30.08.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Poor quality product administered
Product storage error
Symptomtext
ADACEL was administrated post excursion with no reported adverse event; Initial information received on 06-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 65 years old male patient to whom experienced diphtheria-2/tetanus/5 AC pertussis vaccine [Adacel] was administrated post excursion with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 30-Aug-2022, the patient was administrated 0.5 ml dose 1 of suspect diphtheria-2/tetanus/5 AC pertussis vaccine, suspension for injection (lot U7461AA Exp.date: 12-JUL-2024) via intramuscular route in the right arm for immunization post excursion with no reported adverse event (poor quality product administered). Action taken : not applicable. Outcome : Unknown. 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.; Sender's Comments: 01266747: 01266903: 01266768: 01266921: 01266924: 01266780: 01266792: 01266974: 01266976: 01266978: 01266980: 01266982: 01266985: US-SA-2022SA372080:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 29.08.2022
- Beginn
- 29.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
No adverse event
Poor quality product administered
Symptomtext
ADACEL were administrated post excursion with no adverse event; Initial information received on 06-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 58 years old male patient to whom diphtheria-2/tetanus/5 AC pertussis vaccine [Adacel] was administrated post excursion with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 29-Aug-2022, the patient received 0.5 ml dose of suspect diphtheria-2/tetanus/5 AC pertussis vaccine, suspension for injection (lot U7461AA; expiry date: 12-Jul-2024) via intramuscular route in the left arm for immunization On 29-Aug-2022 on same day the Adacel were administrated post excursion with no adverse event (poor quality product administered). Action taken : not applicable. Outcome : Unknown. 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
- Medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 30.08.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Adacel at a low of negative 5.1C out of range for 12 minutes and a low of 1.3C out of range for 10 minutes were administrated post excursion with no AE; Initial information received on 06-Sep-2022 regarding an unsolicited valid non-serious case received from health professional. GMI number: 01266980 This case involves a 33-year-old male patient who experienced Diphtheria-2/Tetanus/5 AC Pertussis Vaccine [Adacel] at a low of negative 5.1c out of range for 12 minutes and a low of 1.3c out of range for 10 minutes were administrated post excursion with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. This case is linked to cases 2022SA370866, 2022SA372086, 2022SA373534, 2022SA371564, 2022SA371948, 2022SA372095, 2022SA372180, 01266982, 2022SA372199, 2022SA373167, 2022SA372080, 2022SA372581 and 2022SA372584. It was reported that a temperature excursion of unknown cause, reporting two excursions occurring overnight, no staff present, no human error. Caller reporting ADACEL at a low of negative 5.1C out of range for 12 minutes and a low of 1.3C out of range for 10 minutes. On 30-Aug-2022, the patient received a dose post excursion of suspect Adacel Vaccine at dose 0.5ml once via intramuscular route in the left arm (lot U7461AA, expiry date: 12-Jul-2024) for immunization with no reported adverse event (poor quality product administered) latency same day. Action taken: Not applicable. At time of reporting, the outcome was Unknown. 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
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 29.08.2022
- Beginn
- 29.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
No adverse event
Poor quality product administered
Product storage error
Symptomtext
Adacel at a low of negative 5.1C out of range for 12 minutes and a low of 1.3C out of range for 10 minutes. with no reported ae; ADACEL (8 doses) were administrated post excursion with no reported adverse event; Initial information received on 06-Sep-2022 regarding an unsolicited valid non-serious case received from other health professional. This case involves a 38 years old male patient and it was reported DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] exposed at a low of negative 5.1c out of range for 12 minutes and a low of 1.3c out of range for 10 minutes with no reported adverse event(AE) and adacel (8 doses) were administrated post excursion with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s), concomitant medication and family history were not provided. On 29-Aug-2022, the patient received suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE at 0.5 ml once (lot U7461AA, expiry date: 12-Jul-2024) via intramuscular route in the right arm for immunisation. On an unknown date the patient adacel was at a low of negative 5.1c out of range for 12 minutes and a low of 1.3c out of range for 10 minutes. with no reported ae (product storage error). On 29-Aug-2022 the patient developed a non-serious adacel (8 doses) were administrated post excursion with no reported adverse event (poor quality product administered) same day latency following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. Action taken: Not applicable. Outcome was Unknown for the event adacel at a low of negative 5.1c out of range for 12 minutes and a low of 1.3c out of range for 10 minutes. with no reported ae and was Unknown for the event adacel (8 doses) were administrated post excursion 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 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.; Sender's Comments: 01266768: 01266921: 01266924: US-SA-2022SA372080:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
at a low of negative 5.1C out of range for 12 minutes and a low of 1.3C out of range for 10 minute with no adverse event; administering dose post temperature excursion with no reported adverse event; Initial information received on 06-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 23 years old female patient who reported administering dose post temperature excursion with no reported adverse event and at a low of negative 5.1c out of range for 12 minutes and a low of 1.3c out of range for 10 minute 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. On 31-Aug-2022, the patient received a 0.5 ml dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE once (1X) ( lot U7461AA; expiry date: 12-JUL-2024) via intramuscular route in the right arm for immunization. On 31-AUG-2022 the patient reported a non-serious event administering dose post temperature excursion with no reported adverse event (poor quality product administered) following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. On an unknown date the patient developed a non-serious at a low of negative 5.1c out of range for 12 minutes and a low of 1.3c out of range for 10 minute with no adverse event (product storage error) (unknown latency) following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. Action taken: not applicable. At time of reporting, the outcome was Unknown for the events. 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.; Sender's Comments: 01266747: 01266903: 01266768: 01266921: 01266924: 01266780: 01266792: 01266974: 01266976: 01266978: 01266980: 01266982: 01266983: 01266985: US-SA-2022SA372080:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 30.08.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
No adverse event
Product storage error
Symptomtext
temperature excursion at negative 5.1 degree Celsius for 12 minutes and a low of 1.3 degree Celsius for 10 minutes with no reported adverse event; vaccine administered post excursion with no reported adverse event; Initial information received on 06-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 11 years old male patient who was administered diphtheria-2/tetanus/5 AC pertussis vaccine [Adacel] post excursion which was at negative 5.1 degree Celsius for 12 minutes and a low of 1.3 degree Celsius for 10 minutes 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 meningococcal vaccine and hpv vaccine. On an unknown date, the suspect diphtheria-2/tetanus/5 AC pertussis vaccine was exposed to a temperature excursion at negative 5.1 degree Celsius for 12 minutes and a low of 1.3 degree Celsius for 10 minutes with no reported adverse event (product storage error). On 30-Aug-2022, the patient received a0.5 mL dose of suspect diphtheria-2/tetanus/5 AC pertussis vaccine (formulation and strength not reported; lot U7461AA, expiry date: 12-Jul-2024) via intramuscular route in the right arm for prophylactic immunization. On 30-Aug-2022, (latency: same day) the patient was administered diphtheria-2/tetanus/5 AC pertussis vaccine post excursion with no reported adverse event (poor quality product administered). Action taken was not applicable. At time of reporting, the outcome was Unknown for both the events. 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.; Sender's Comments: General 01266747: Daptacel 01266903: ACTHIB 01266768: ACTHIB 01266921: ACTHIB 01266924: MENACTRA 01266780: ADACEL 01266792: ADACEL 01266974: ADACEL 01266976: ADACEL 01266978: ADACEL 01266980: ADACEL 01266982: ADACEL 01266983: ADACEL 01266985:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 23.08.2022
- Beginn
- 23.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- 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
Symptomtext
Child (2.5 years) was given Adacel inadvertently by HCP with no reported adverse event; Initial information received on 23-Aug-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 28 months old female patient who was given adacel inadvertently by health care professional with no reported adverse event, after 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. On 23-Aug-2022, the patient received a total dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE( lot U7461AA) at 0.5ml once via intramuscular route in unknown administration site for Immunization.. On 23-Aug-2022(latency: same day), the patient was given adacel inadvertently by health care professional with no reported adverse event (product administered to patient of inappropriate age)(latency: same day) following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. Action taken : not applicable. It was not reported if the patient received a corrective treatment for the event. Outcome: unknown 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
- IL
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 23.08.2022
- Impfdatum
- 23.08.2022
- Beginn
- 23.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
Tdap inadvertently given instead of DTaP. this was to be his 4th shot in the series. no symptoms at present
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 20.03.2017
- Beginn
- 12.08.2022
- Tage bis Beginn
- 1.971,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
A Tdap was given instead of a Dtap. Mother informed and apologized to . Informed her of the recommendation to get Dtap in 4 weeks . also informed her that the injection that was given was a lesser strength than what she should have received. Mom does not want to get the Dtap in 4 weeks as recommended.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -