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Reporte zur Charge U009261

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

13Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CO 3 WA 2 TX 1 KS 1 FL 1 MT 1 UT 1 OK 1 CA 1 IL 1

VAERS 1825079

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge U009261

schwer
Staat
TX
Alter
13,0
Geschlecht
M
Eingang
28.10.2021
Impfdatum
28.10.2021
Beginn
28.10.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Pallor Syncope

Symptomtext

After vaccines were administered, the child stood up abruptly and swayed. The nurse asked if he felt all right and he said yes, and almost immediately fainted. He was caught before he hit the floor. Ammonia salts were utilized and he revived immediately and tried to stand. Nurse and MA kept the child in a prone position for approximately ten minutes. When asked, he said he ate a little yogurt for breakfast. Mom stayed on her phone. When helped to a sitting position in a chair, the child lost color in his face again and dropped something from his hand. MA and nurse wheeled the child to a sofa in an employee break room. When given water, he drank it very thirstily and stated he had not had anything to drink all day. Mom gave child a juice box which he drank completely. He stayed on the sofa for approximately 20 minutes. He had some shivering. As he would drink fluids, he would regain color in his lips and face. After a few minutes post-hydration, his color would pale again. Mom remained on her phone, while stating to clinic staff that "he got too many shots." (The child, a recent immigrant, did not have requisite vaccinations to enroll in school. He received the five necessary vaccination for enrollment, and Mother requested that HPV be given also.) Mother was educated about eating and drinking before the next visit and if the child needed further medical attention, to take the child to his doctor or an Urgent Care near their home. The vaccines were administered at 10;40 and the family departed the clinic at 11:20.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
None known.
Aktuelle Erkrankungen
None known or reported.
Vorgeschichte
None known or reported.
Andere Medikamente
None known.
Allergien
NKA
Vorherige Impfungen
-

VAERS 2284899

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge U009261

mild
Staat
KS
Alter
5,0
Geschlecht
F
Eingang
19.05.2022
Impfdatum
09.05.2022
Beginn
17.05.2022
Tage bis Beginn
8,0
Dosis
2
Route/Site
SC / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pyrexia

Symptomtext

Client's mother called 5-18-2022 and stated that her daughter started developing a fever during the evening of 5-17-2022 that got up to the high of 103 degrees. Mother gave client tylenol around the clock which helped bring down the fever, but mother stated clients fever went back up to a high of 102 degrees 5-18-2022. Clients mother states her daughter is acting completely fine and normal other than having the fever.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 1788606

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge u009261

mild
Staat
FL
Alter
4,0
Geschlecht
F
Eingang
15.10.2021
Impfdatum
08.10.2021
Beginn
08.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site pain Injection site swelling

Symptomtext

Mother came in for another appointment a week after vaccine administration and mentioned pt has been complaining of pain and swelling at injection site. Mother had not medicated. Informed mother to give Tylenol for pain, mother voiced understanding.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
Astigmatism
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2481841

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge U009261

gering
Staat
CO
Alter
12,0
Geschlecht
M
Eingang
18.10.2022
Impfdatum
18.10.2022
Beginn
18.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered No adverse event

Symptomtext

Expired Vaccine, no adverse reaction

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
None
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2426108

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge U009261

gering
Staat
CO
Alter
-
Geschlecht
U
Eingang
01.09.2022
Impfdatum
01.08.2022
Beginn
01.08.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered No adverse event

Symptomtext

I have not noticed any adverse effects at this time; misread the label when pulling MMR out of the freezer, believed at the time of pulling the vaccine that MMR was in the freezer with VARIVAX, the vaccine in the freezer was actually Proquad; varivax and proquad administered the same day misread the label when pulling MMR out of the freezer, believed at the time of pulling the vaccine that MMR was in the freezer with VARIVAX, the vaccine in the freezer was actually Proquad; did not double checked the vial on the vaccine to make sure it was the right medication; This spontaneous report has been received from a registered nurse concerning a patient of unknown age and gender. Information regarding the patient's pertinent medical history, concurrent conditions and concomitant medications was not provided. On 01-AUG-2022 at 13:45, the patient was vaccinated with the first dose of varicella virus vaccine live (Oka/Merck)(VARIVAX) in the right arm for prophylaxis, lot #U015689, expiration date was not provided, however, upon internal validation was confirmed to be 18-MAY-2023 (strength, dose, frequency and route of administration were not provided). On the same date, the registered nurse administered in error a dose of measles, mumps, rubella and varicella (oka-merck) virus vaccine live (PROQUAD) subcutaneously in the left arm also for prophylaxis lot #U009261, expiration date was not provided, however, upon internal validation was confirmed to be 19-SEP-2022 (strength, dose and frequency were not reported) asat the time of pulling the vaccine out from the freezer he took the measles, mumps, rubella and varicella (oka-merck) virus vaccine live (PROQUAD) instead of Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (MMR-II) vaccine. The registered nurse reported that the patietn was scheduled to receive five vaccines which included hib vaccine conj (tet tox) (ACT-HIB), pneumococcal vaccine conj 13v (crm197) (PREVNAR 13) and hepatitis a vaccine inact (HEP A IN VAC). On the same date, the registered nurse notified the vaccination error to the patient's mother, she inquired regarding the possible adverse effects that double vaccination with varicella vaccine, however, the patient's mother informed that the patient had no experienced any adverse effect from the vaccines.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
ACT-HIB; PREVNAR 13; HEP A IN VAC
Allergien
-
Vorherige Impfungen
-

VAERS 2408966

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge U009261

gering
Staat
CO
Alter
1,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
01.08.2022
Beginn
01.08.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered Wrong product administered

Symptomtext

On 08/01/2022 at approximately 01:45 PM, RN administered MMRV (Measles, Mumps, Rubella and Varicella) vaccine in error to pt. in left upper arm subcutaneously in the child clinic room. Pt. was scheduled to receive five vaccines today which included pediatric Hepatitis A (Hep A), Pneumococcal conjugate (PVC-13), Haemophilus Influenza type B (Hib), Measles, mumps, rubella (MMR), and Varicella (VAR-Varivax). RN misread the vaccination label when pulling MMR out of the freezer. RN believed at the time of pulling the vaccine, that MMR is in the freezer with VAR. The vaccine in the freezer was actually measles, mumps, rubella and varicella (MMRV-Proquad) Both MMRV and VAR were labeled as state vaccines. Which at the time, I believed the patient to be eligible. RN did not complete one of my six rights of administration by double checking the vial on the vaccine to make sure it was the right medication. I believe if I had completely turned the vaccine vial, I would have read the entire label. RN made a telephone call to parent at approximately 03:10 PM to notify her that her son received a double dose of the VAR which is a live vaccine, I relayed side effects of vaccines and what to watch out such as increase in fever, redness, soreness and pain at injection site and irritability. Parent asked RN "is my son going to come down with chicken pox later and possibly give it to my other son?", and RN replied, "he is not likely to come down with chicken pox and become contagious" Parent had no further question and she was given my name and the name of my immediate supervisor to call if she had additional questions. Parent did not notice any adverse effects of vaccine at this time but stated to the effect "I will keep an eye on him" At 05:02 RN made call to Merck, the vaccine manufacturer to get additional information on other adverse effects. RN spoke with Merck. Rep relayed that Merck showed no other adverse effects than those side effects listed for each vaccine as Fever, Irritability, redness, soreness or pain at the injection site, and that contracting chicken pox was not listed as an adverse event, side effect when the two vaccines MMRV (Proquad) and Var (Varivax) were given together. Rep at Merck is to provide information via email on findings with RN. At 05:21 PM, RN made additional call to parent on MERCK findings on adverse events, side effects when taking Proquad and Varivax together and that there were no findings to support that patients contracted chicken pox after vaccination. RN to email copy of findings from Merck to parent once received. RN asked parent how her son was doing now and she replied "he is resting now as he typically does after vaccination, I gave him pediatric Tylenol before resting, but I have not noticed any adverse effects at this time". She thanked me for the information and stated she would call if she had questions. On 8/2/2022 at 9:20 AM Information was sent to parent at the email provided from parent, she stated to the effect that this was an old work email she had kept and had been using and never changed it. Parent was given information provided in attachments from Merck. On 8/2/2022 at 3:46 PM, RN made a call to parent, I received her voice mail and a voice mail message was left by me asking parent is she had received my email with the information and to call if she had any questions, in addition RN asked parent on the well being of her son. On 8/3/2022 RN's supervisor made follow up telephone call to parent to inquire on well being of her son, There was no answer, a message was left for parent to return call. No call back known to be received and no return messages were left. Result of outcome of adverse event(s) is unknown due to no follow up response from Patient's parent.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
Unkown
Aktuelle Erkrankungen
Parent denies current illness, unkown up to one month prior.
Vorgeschichte
None reported by parent at time of vaccination.
Andere Medikamente
Unkown
Allergien
Parent denies allergies to medication or foods.
Vorherige Impfungen
-

VAERS 2400531

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge U009261

gering
Staat
MT
Alter
3,0
Geschlecht
F
Eingang
03.08.2022
Impfdatum
01.08.2022
Beginn
01.08.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
SC / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered

Symptomtext

Patient was given Pfizer 5-<12 and should have been given Pfizer 6 months-4 years. Parent informed at appointment. Patient tolerated all vaccines given. This nurse has not had any other further conversation with the parent at the time of completing this form.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
None listed
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2316236

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge U009261

gering
Staat
UT
Alter
19,0
Geschlecht
U
Eingang
11.06.2022
Impfdatum
-
Beginn
16.05.2022
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Wrong product administered

Symptomtext

This spontaneous report was received from a medical assistant referring a 19-year-old patient. The patient's pertinent medical history, previous drugs reactions or allergies and concomitant medications were not reported. On an unknown date, the patient was vaccinated with measles, mumps, rubella and varicella (oka-merck) virus vaccine live (recombinant human albumin (rHA)) (PROQUAD) lot number U009261, expiration date: 19-SEP-2022 (strength, vaccination scheme, route of administration and anatomical location were not reported); the patient was intended to receive varicella virus vaccine live (oka/merck) (VARIVAX) (strength, vaccination scheme, dose description, lot number, expiration date, route of administration and anatomical location were provided); and measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (M-M-R II) (strength, vaccination scheme, dose description, lot number, expiration date, route of administration and anatomical location were not provided) it was stated that the event was due to a medical error (wrong product administered). No additional adverse event was reported.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2200347

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge u009261

gering
Staat
OK
Alter
1,6
Geschlecht
U
Eingang
26.03.2022
Impfdatum
09.03.2022
Beginn
09.03.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inappropriate schedule of product administration No adverse event

Symptomtext

Confirmed wtih caller no other AE occurred.; The caller reported a patient received both PROQUAD and VARIVAX on 09-MAR-2022; This spontaneous report was received from a nurse and refers to a 19-month-old patient. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 09-MAR-2022, the patient was vaccinated with measles, mumps, rubella and varicella (oka-merck) virus vaccine live, recombinant Human albumin (rHA) (PROQUAD) 1 dose, lot # u009261, expiration date: 19-SEP-2022 (formulation, dose, strength, site and route of administration were not provided) for prophylaxis; and varicella virus vaccine live (oka/merck) (VARIVAX) 1 dose, lot # t040418, expiration date: 01-DEC-2022 (formulation, dose, strength, site and route of administration were not provided) for prophylaxis (Inappropriate schedule of product administration). No other adverse event occurred (No adverse event).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1939824

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge U009261

gering
Staat
WA
Alter
6,0
Geschlecht
M
Eingang
10.12.2021
Impfdatum
10.12.2021
Beginn
10.12.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
SC / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Underdose

Symptomtext

Patient was noncompliant during administration of MMRV vaccine and I was only able to administer half of the dose before he moved and I had to remove the needle. The provider was informed of this immediately and spoke with parents, who decided to come back in one month for a repeat dose. Patient left clinic about 5-10 minutes later and had no other issues.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Underdose
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Multivitamin
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 1800171

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge U009261

gering
Staat
WA
Alter
-
Geschlecht
F
Eingang
20.10.2021
Impfdatum
30.09.2021
Beginn
30.09.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

No additional adverse events reported; A 15 year ald female received PROQUAD yesterday; This spontaneous report was received from a registered nurse and refers to a 15 year old female patient. The patient's pertinent medical history, concurrent conditions and concomitant medications were not reported. On 30-SEP-2021, the patient was vaccinated with measles, mumps, rubella and varicella (oka-merck) virus vaccine live(PROQUAD) (lot # U009261, expiration date: 19-SEP-2022) 1 dose in the left deltoid for prophylaxis (product administered to patient of inappropriate age). No additional adverse events reported.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1770263

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge U009261

gering
Staat
CA
Alter
-
Geschlecht
U
Eingang
08.10.2021
Impfdatum
28.09.2021
Beginn
28.09.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product storage error

Symptomtext

?? symptoms were reported/ No additional AE's; PROQUAD was administered to (1) patient ?? 9/28/21; with the initials ED, after the excursion.; This spontaneous report was received from a medical assistant and refers to a patient of unspecified age and gender. The patient's pertinent medical history, concomitant medications, past drug reactions or allergies were not reported. On 28-SEP-2021, the patient was vaccinated with Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live rHA (recombinant Human albumin) (PROQUAD) Dose/Frequency reported as 1 (concentration, vaccination scheme frequency, route and anatomical site of administration were nor provided; lot number U009261 that was verified to be a valid lot number with an expiration date reported and established as 19-SEP-2022) for prophylaxis after underwent a temperature excursion of 33.1 degrees Fahrenheit (F) during a time frame of 4 hours and 15 minutes. No symptoms or additional adverse events (AEs) were reported

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1630956

MERCK & CO. INC. · MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) · Charge U009261

gering
Staat
IL
Alter
4,0
Geschlecht
M
Eingang
25.08.2021
Impfdatum
16.08.2021
Beginn
16.08.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product storage error

Symptomtext

no additional adverse experience; Improperly stored vaccine administered; This spontaneous report as received from a nurse refers to a 4-year-old male patient. Pertinent medical history, drug reactions, allergies and concomitant medications were not reported. On 16-AUG-2021, the patient was vaccinated with an improperly stored dose of measles, mumps, rubella and varicella (oka-merck) virus vaccine live (rHA) (PROQUAD) (lot number: U009261, expiration date: 19-SEP-2022; dose and route of administration not provided). The vaccine was stored in temperature 38 degrees Fahrenheit for 67 hours 30 minutes and 0 seconds. There was no previous temperature excursion. No adverse event was reported.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-