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Reporte zur Charge AU3835E

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
GA 3 CO 1

VAERS 2698411

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AU3835E

moderat
Staat
CO
Alter
52,0
Geschlecht
F
Eingang
19.10.2023
Impfdatum
12.10.2023
Beginn
13.10.2023
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Arthralgia Asthenia Gait disturbance Mobility decreased Muscle spasms Muscular weakness Pelvic pain

Symptomtext

Developed severe sacrum, pelvic, and hip flexor pain. Muscle spasms across front of pelvic girdle. Could not move without assistance. Weakness through lower back and sides, gait disturbance. ER physician administered the following via IV: Decadron Dilaudid Toradol Robaxin lactated ringers lidocaine patch Prescribed course of methylPREDNISolone

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Zoloft, B vitamins, fish oil, D+K combo
Allergien
cumin (the spice)
Vorherige Impfungen
Pelvic girdle pain, muscle weakness; COVID Moderna Bivalent, 10/22/2022; age 51

VAERS 2697890

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge au3835e

mild
Staat
GA
Alter
72,0
Geschlecht
F
Eingang
18.10.2023
Impfdatum
14.10.2023
Beginn
16.10.2023
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site pain

Symptomtext

Patient got spikevax on 10-14-23 IM in the left arm. Two days later the patient started having intermittent sharp pain lasting up to 30 seconds at and around the injection site. She did not take anything to treat the pain. She did not check for any redness, heat or swelling. She still had the bandaid on from the vaccine administraion. We went to the vaccine room and she removed the bandaid. No redness, swelling or heat was found. I encouraged the patient to continue to moniter her arm and seek medical attention if the pain worsened or if it started showing signs of infection. She agreed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
amlodipine 10, diclofenac 75, diclofenac gel, indapamide 1.25, klor-con m20, bisoprolol 10, telmisartan 80, atorvastatin 40, aspirin
Allergien
boostrix, hydralazine. pantoprazole
Vorherige Impfungen
-

VAERS 2697369

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge AU3835E

mild
Staat
GA
Alter
68,0
Geschlecht
F
Eingang
17.10.2023
Impfdatum
12.10.2023
Beginn
12.10.2023
Tage bis Beginn
0,0
Dosis
5
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site haemorrhage

Symptomtext

The pharmacy technician stated that they were able to inject the vaccine but when the syringe was pulled out, the patient bled profusely from the site of the injection.; This spontaneous case was reported by a pharmacist and describes the occurrence of INJECTION SITE HAEMORRHAGE (The pharmacy technician stated that they were able to inject the vaccine but when the syringe was pulled out, the patient bled profusely from the site of the injection.) in a 68-year-old female patient who received mRNA-1273.815 (SPIKEVAX 2023-2024) (batch no. AU3835E) for COVID-19 prophylaxis. Concurrent medical conditions included Osteoporosis. Concomitant products included INFLUENZA VACCINE for an unknown indication. On 12-Oct-2023, the patient received fifth dose of mRNA-1273.815 (SPIKEVAX 2023-2024) (Intramuscular use) .5 milliliter. On 12-Oct-2023, after starting mRNA-1273.815 (SPIKEVAX 2023-2024), the patient experienced INJECTION SITE HAEMORRHAGE (The pharmacy technician stated that they were able to inject the vaccine but when the syringe was pulled out, the patient bled profusely from the site of the injection.). At the time of the report, INJECTION SITE HAEMORRHAGE (The pharmacy technician stated that they were able to inject the vaccine but when the syringe was pulled out, the patient bled profusely from the site of the injection.) outcome was unknown. For mRNA-1273.815 (SPIKEVAX 2023-2024) (Intramuscular use), the reporter did not provide any causality assessments. Treatment medications were not reported.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site haemorrhage
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Osteoporosis
Vorgeschichte
-
Andere Medikamente
INFLUENZA VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 2693106

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge AU3835E

mild
Staat
-
Alter
70,0
Geschlecht
F
Eingang
09.10.2023
Impfdatum
03.10.2023
Beginn
03.10.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Injection site erythema Injection site warmth Peripheral swelling Rash erythematous Rash pruritic

Symptomtext

she experienced swelling in left arm,; she has redness in the upper arm at injection site and down where arm bends and red around the inside of the arm.; The arm feels hot around the area touch.; a rash, it was itchy, red,; a rash, it was itchy, red,; she has redness in the upper arm at injection site; This spontaneous case was reported by a patient and describes the occurrence of PERIPHERAL SWELLING (she experienced swelling in left arm,), ERYTHEMA (she has redness in the upper arm at injection site and down where arm bends and red around the inside of the arm.), FEELING HOT (The arm feels hot around the area touch.), RASH ERYTHEMATOUS (a rash, it was itchy, red,) and RASH PRURITIC (a rash, it was itchy, red,) in a 70-year-old female patient who received mRNA-1273.815 (SPIKEVAX 2023-2024) (batch no. AU3835E) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Lymph node excision (Patient had surgery to remove lymph node in 2021 in the left arm) in 2021 and Radiation therapy. On 03-Oct-2023, the patient received fourth dose of mRNA-1273.815 (SPIKEVAX 2023-2024) (unknown route) 1 dosage form. On 03-Oct-2023, the patient experienced PERIPHERAL SWELLING (she experienced swelling in left arm,), ERYTHEMA (she has redness in the upper arm at injection site and down where arm bends and red around the inside of the arm.), FEELING HOT (The arm feels hot around the area touch.), RASH ERYTHEMATOUS (a rash, it was itchy, red,), RASH PRURITIC (a rash, it was itchy, red,) and VACCINATION SITE ERYTHEMA (she has redness in the upper arm at injection site). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at an unspecified dose and frequency. At the time of the report, PERIPHERAL SWELLING (she experienced swelling in left arm,), ERYTHEMA (she has redness in the upper arm at injection site and down where arm bends and red around the inside of the arm.), FEELING HOT (The arm feels hot around the area touch.), RASH ERYTHEMATOUS (a rash, it was itchy, red,), RASH PRURITIC (a rash, it was itchy, red,) and VACCINATION SITE ERYTHEMA (she has redness in the upper arm at injection site) had not resolved. No relevant concomitant medications were reported. Patient reported that she received Spikevax on 03Oct2023, and during the night she experienced swelling in left arm, a rash, it was itchy, red, she has redness in the upper arm at injection site and down where arm bends and red around the inside of the arm. The arm felt hot around the area touch. Treatment included allergy medication, and cream for rash. This case was linked to US-MODERNATX, INC.-MOD-2023-744296 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-744296:Monovalent dose

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Lymph node excision (Patient had surgery to remove lymph node in 2021 in the left arm); Radiation therapy
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2691703

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge AU3835E

gering
Staat
GA
Alter
71,0
Geschlecht
F
Eingang
05.10.2023
Impfdatum
30.09.2023
Beginn
01.10.2023
Tage bis Beginn
1,0
Dosis
6
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dry eye Dry mouth Erythema Skin warm

Symptomtext

PT COMPLAINS OF SKIN ERYTHEMA, SCALP IS HOT, NO ITCHING; EYES AND MOUTH ARE EXTREMELY DRY

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dry eye
Hospital-Tage
-
Labordaten
N/A PT HAS SCHEDULED APPOINTMENTS WITH OPTHALMOLOGIST AND DERMATOLOGIST
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
NSAID'S
Vorherige Impfungen
-