- Staat
- FL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 29.09.2023
- Beginn
- 05.10.2023
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram
Cerebrovascular accident
Computerised tomogram
Magnetic resonance imaging
Symptomtext
I had a stroke on October 5. I had no preexisting conditions such as high blood pressure, high cholesterol, etc. I never get sick and work out regularly. I also received the Flucel Vax Quad from Sequirus (Lot 944447) on the same day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 22,0
- Labordaten
- 1 MRI 3 CT scans 3 Angiograms
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 21.11.2023
- Impfdatum
- 01.11.2023
- Beginn
- 02.11.2023
- Tage bis Beginn
- 1,0
- Dosis
- 6
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest X-ray
Computerised tomogram head
Electrocardiogram
Full blood count
Immunisation reaction
Influenza A virus test
Influenza B virus test
Metabolic function test
SARS-CoV-2 test
Syncope
Troponin I
Urine analysis
Symptomtext
syncopal episode within 24 hours of injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- ED visit on 11/02/23, received CT of head, ECG-12 lead, Chest X-ray, UA dipstick, Troponin I, CBC, CMP, Influenza A, B, COVID-19, Attending MD Emergency Medicine DX Vasovagal Syncope likely r/t recent vaccination Treatment NS infusion
- Aktuelle Erkrankungen
- Dementia, anxiety, polyneuropathy, purpura, hypertension
- Vorgeschichte
- Dementia, anxiety, polyneuropathy, purpura, hypertension
- Andere Medikamente
- Celebrex, citalopram, miralax, olanzepine 2.5 mg in pm, preservision, senokot, quetiapine 50 mg in am, acetaminophen, lorazepam
- Allergien
- none known at time of vaccination
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 20.11.2023
- Impfdatum
- 17.11.2023
- Beginn
- 17.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- 7+
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Syncope
Symptomtext
Patient received 2 vaccines around 2:40pm , after 2-3 hours she was shopping at store and felt like she was going to faint. She fainted at the register and the ambulance took her to the hospital. She informed us of this on Sunday and said her blood pressure was 77/___. She couldn't remember the entire blood pressure. Per the patient, they gave her a bolus of saline. She told us the medical personnel thought she was dehydrated. She also informed us that she had only eaten 2 cookies that morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- adhesive tape, NSAIDS, and penicillin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 17.11.2023
- Impfdatum
- 10.11.2023
- Beginn
- 10.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Pain in extremity
Symptomtext
After receiving vaccine patient had painful arm, difficulty raising arm lasting 1+ week. Tylenol not helping Informed patient to contact provider
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Thyroid, HBP,
- Andere Medikamente
- Gabapentin 100mg, Citalopram 10mg, Prednisone 10mg, Ropinirole, Levothyroxine, Lisinopril
- Allergien
- Acetaminophen, Codeine
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 04.11.2023
- Impfdatum
- 04.11.2023
- Beginn
- 04.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chills
Eye movement disorder
Hyperhidrosis
Immediate post-injection reaction
Posture abnormal
Somnolence
Tremor
Symptomtext
Flucelvax was given first in the left deltoid, the patient responded fine. Then approximately 30 seconds later the Spikevax was administered, also in the left arm, approximately 2 inches away from the administration site of the Flucelvax. The patient's head drooped forward immediately when the injection started going into the muscle. I then took the needle out to discontinue the administration. The patient had a full body rigor, head dropped back, her eyes rolled back in her head and she started shaking. The patients mother and I called her name and she was then alert, but drowsy and diaphoretic. 911 was called, blood pressure taken (86/64 ). I stayed with the patient and mom while we waited for emergency services to arrive. The patient was given some water and stayed alert until EMT's arrived. Patient and mother were transported to Hospital Emergency Department.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- 11/4/23 Blood pressure 86/64
- Aktuelle Erkrankungen
- None at time of vaccination. Prior illness unknown.
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 11.10.2023
- Impfdatum
- 04.10.2023
- Beginn
- 04.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Muscle fatigue
Myalgia
Pyrexia
Tremor
Symptomtext
muscle fatigue; shaking; muscle soreness; temperature increase; chills; This spontaneous case was reported by a patient and describes the occurrence of MUSCLE FATIGUE (muscle fatigue), TREMOR (shaking), MYALGIA (muscle soreness), PYREXIA (temperature increase) and CHILLS (chills) in a 25-year-old female patient who received mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) (batch no. 3032218) for COVID-19 prophylaxis. Co-suspect product included non-company product INFLUENZA VACCINE for an unknown indication. The patient's past medical history included Coughing (Took Mucinex DM for coughing.) and COVID-19 (Once around Mar-2022 during 3 to 5 days) in March 2022. Previously administered products included for Coughing: Mucinex DM. Past adverse reactions to the above products included No adverse event with Mucinex DM. On 04-Oct-2023, the patient received dose of INFLUENZA VACCINE (unknown route) 1 dosage form. On 04-Oct-2023 at 11:30 AM, the patient received fifth dose of mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) (unknown route) .5 milliliter. On 04-Oct-2023, the patient experienced MUSCLE FATIGUE (muscle fatigue), TREMOR (shaking), MYALGIA (muscle soreness), PYREXIA (temperature increase) and CHILLS (chills). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency and CAFFEINE, PARACETAMOL (EXCEDRIN [CAFFEINE;PARACETAMOL]) at an unspecified dose and frequency. At the time of the report, MUSCLE FATIGUE (muscle fatigue), TREMOR (shaking), PYREXIA (temperature increase) and CHILLS (chills) was resolving and MYALGIA (muscle soreness) had not resolved. For mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) (Unknown), the reporter did not provide any causality assessments. Concomitant medication use information was not provided by reporter. On 03-Jan-2021, the patient received first dose of Pfizer and the lot number was EJ1686. On 20-Jan-2021, the patient received second dose of Pfizer and the lot number was EL3248. On 20-Nov-2021, the patient received third dose of Pfizer and the lot number was FD0809. On 05-Nov-2022, the patient received fourth dose of Pfizer and the lot number was GJ6738. The patient has received other vaccines in the 4 weeks prior to COVID-19 vaccine. The patient had her Spikevax appointment at her work at 11:30 AM and started feeling symptoms when she was driving home approximately at 5 or 6 PM, initially felt muscle fatigue and then headedness, later on she felt temperature increase and chunk chills, she was shaking a lot, and feeling muscle soreness. Caller took Tylenol and Excedrin. Muscle soreness was still ongoing. The patient got flu vaccine at same time than Spikevax but in a different arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Coughing (Took Mucinex DM for coughing.); COVID-19 (Once around Mar-2022 during 3 to 5 days)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 05.10.2023
- Impfdatum
- 04.10.2023
- Beginn
- 04.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amnesia
Dizziness
Dysgeusia
Fatigue
Injected limb mobility decreased
Injection site erythema
Injection site pain
Injection site swelling
Injection site warmth
Pain
Vision blurred
Symptomtext
after an hour had metallic taste in my mouth, felt faint. as fast as it came it disappeared as fast. Eyesight reading letters were blurry, an memory for spelling not good. Then got tired my usual reaction to preservatives, took a couple of naps most of the afternoon. Whole body started to ache. Around 8pm site started to hurt, got swollen and red. Now today the only problem is the site is warm and red and hard to raise my arm. Otherwise seem ok. Was concerned as i have A fib with a pacemaker. Cardiologist said they could not see any a fib episodes for yesterday and this morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- -
- Allergien
- preservatives
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 29.12.2023
- Impfdatum
- 06.12.2023
- Beginn
- 18.12.2023
- Tage bis Beginn
- 12,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pain
Pruritus
Urticaria
Symptomtext
12 days after the booster shot, I started developing painful and itchy hives. I was prescribed a 15 day course of Prednisone 10 mg (4 tabs x 5 days, 2 tabs x 5, 1 tab x 5 days). I've also been taking 4 Benedryl per day, 1 Zyrtec per day, and occasional famotidine 20 mg. The hives are still present and still itchy after 10 days of treatment. The reason I believe this is caused by the vaccine is because two years ago the exact same thing happened to me after receiving the Moderna booster. However, at the time doctors attributed the hives to an antibiotic. At that time, I had developed an infection at the injection site and was put on a strong antibiotic. 11 days after receiving that shot, I broke out in hives. In the same manner, I was prescribed a steriod to deal with the hives. They were very present for about a month and then occasionally for up to six months afterward.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- No tests were completed. Only visual observations and medical messaging.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- kidney stones
- Andere Medikamente
- Escitalopram 10mg, Zyrtec, magnesium, symplex F,
- Allergien
- no
- Vorherige Impfungen
- Date: 11/19/2021, Moderna 100mcg/0.5ml PF, MDV, Lot #058H21A at Pharmacy, patient age was 43, same effect - developed hives 11 d
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 20.11.2023
- Impfdatum
- 20.10.2023
- Beginn
- 21.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- 6
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Bursitis
Joint range of motion decreased
Product administered at inappropriate site
Symptomtext
Covid 19 vaccination found to have been injected into left subacromial bursa instead of deltoid muscle causing a severe acute subacromial bursitis characterized by pain and limited range of motion of the shoulder.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Ongoing advanced endometrial cancer
- Vorgeschichte
- As noted above
- Andere Medikamente
- Lisinopril Lenvima Amlodipine
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 13.11.2023
- Impfdatum
- 26.10.2023
- Beginn
- 26.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blindness unilateral
Dizziness
Fatigue
Gait disturbance
Symptomtext
Patient says that she lost vision in her left eye about 45 minutes to an hour after receiving her vaccinations. She was aslo extremely fatigued and went to lay down. She woke up the next morning, told a friend about the incident but did not seek any medical intervention. She also told her friend she felt a little dizzy, was swaying , and staggering when she woke up but that resolved itself as the day progressed. Her vision loss had also resolved itself the next morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Fluzone quadrivalent high dose
- Vorgeschichte
- Patient has a pace maker
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 10.11.2023
- Impfdatum
- 08.11.2023
- Beginn
- 09.11.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Injection site discomfort
Injection site erythema
Injection site mass
Symptomtext
Patient came in 2 days after injection and stated she developed a lump with redness around it a day after the vaccination. They adverse reaction was not at the injection site. It is located approximately 3 to 4 inches below the injection site. She also stated that at the time of vaccination, it felt like there were metal pieces also being injected. The vaccine was a prefilled syringe (Moderna's Spikevax). I advised the patient to mark the borders of the redness and to follow up with her physician if it continues to get worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discomfort
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 31.10.2023
- Beginn
- 01.11.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Fatigue
Myalgia
Pyrexia
Symptomtext
Influenza symptoms of sore muscles, sore joints, mild fever, fatigue. Duration of awakening 11/01/23 through Morning of 11/02/23. A period of about 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Coronary Artery Disease.
- Andere Medikamente
- Vascepta2gm, 2 cinnamon capsules 2000mg, AREDS 2 multi vitamin, Vitamin D 200mcg, CoQ10 300mg, Aspirin 81mg
- Allergien
- Lipitor, Crestor, shell fish, eggs, gluten, hops, barley, cats, dogs, horses, most pollens, dusts and molds.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 23.10.2023
- Beginn
- 23.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Exposure via skin contact
Product leakage
Symptomtext
PATIENT CLAIMS THAT SHE FELT A DROP DRIPPING ON HER ARM DURING VACCINATION. PHARMACISTS EXPLAINED THAT THERE COULD BE A LEAKAGE DURING ADMINISTRATION; HOWEVER, SHE STILL RECIEVED FULL DOSE. ALSO, PATIENT CLAIMED THAT SHE FELT DIZZY AND LIGHTHEADED AT CHECK-OUT AFTER MORE THAN 2 HOURS OF SHOPPING WHICH INCLUDED CONTINUOUS WALKING, LIFTING ITEMS, BENDING, AND MULTIPLE SUDDEN TEMPERATURE CHANGES AT FROZEN ISLE. VACCINES WERE GIVEN AT 01:54PM AND SHE FELT LIGHTHEADED AT 04:03PM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO ILLNESS AT THE TIME OF VACCINATION
- Vorgeschichte
- NOT KNOWN TO PHARMACY
- Andere Medikamente
- NOT KNOWN TO PHARMACY
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 02.11.2023
- Impfdatum
- 30.09.2023
- Beginn
- 09.10.2023
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Vertigo
Symptomtext
9 days after vaccine pt stated severe vertigo and dizziness that required hospitalization for 7 hours. Dr. stopped levothyroxine. As of 11.2.23 symptoms have not resolved-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 31.10.2023
- Beginn
- 31.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Immediate post-injection reaction
Pain
Pain in extremity
Wrong technique in product usage process
Symptomtext
JE was administered first without issue. Then almost immediately after injection with COVID, patient reported a shooting pain that blossomed down her arm and radiated to finger tips causing some numbness. As I sat with her for 15 minutes, it began to subside. By the time I left, just a bit of numbness in fingers remained. Needle most likely hit a nerve. Counseled patient to keep moving and that I would check in on her later this afternoon. Upon calling her a few hours later, she reports pain and numbness mostly gone, just may be a bit of residual numbness in pinky finger. She will let me know if it does not subside or worsens.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 29.10.2023
- Impfdatum
- 01.10.2023
- Beginn
- 10.10.2023
- Tage bis Beginn
- 9,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Injection site pain
Lymphadenopathy
Pruritus
Rash
Urticaria
Symptomtext
1) Muscle pain in upper left arm, almost immediately after injection, not treated, disappeared after approx. 3 days 2) Fatigue, next morning after injection, not treated, disappeared after 1 day 3) Swelling and sensitivity of lymph node in left armpit next day after injection, not treated, disappeared after approx. 3 days 4) Minor headache next day after after injection, not treated, disappeared same day 5) Spontaneously occuring extreme itchiness of skin in various places at various times all over my body, initially without any other visual signs. After approx. 2-3 days, minor rashes and welts would appear in same place where itichness was occuring. Rash, welts, and severe itchiness of skin suddenly appear in 2-3 different spots simultaneously, duration approx. 30-60 minutes, then disappear only to re-appear at different parts of body and so on. Itchiness feels like it's coming from inside of body (internal) as opposed to stemming from an external source. First occurred approx. 10 days after injection. From 10/17/2023 treated with L-Carnitin and Alpha Lipoic Acid supplements, resulting in no relief of symptoms. Then treated with 1 tablet daily Antihistamine Fexofenadine HCI 180 mg starting 9:00pm 10/19/2023 resulting in significant reduction of all symptoms from next morning. Discontinued treatment after 3 doses (10/19, 10/20, 10/21), resulting in return of all symptoms from 10/23 onwards. Was hoping that symptoms would dissipate, however since they continued with same severity, restarted prior Antihistamine treatment as before at 9:00pm on 10/28, resulting in significant reduction of symptoms from this morning (10/29).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None so far
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure, Severe Obstructive Sleep Apnea
- Andere Medikamente
- Amlodipine, Ramipril, Rosuvastatin, Testosterone
- Allergien
- Kiwi
- Vorherige Impfungen
- All events described No. 18 above EXCEPT itchiness, ages 52 - 54, vaccination dates 3/12/2021, 4/9/2021, 11/2/2021, 4/6/2022, 12
- Staat
- ND
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 24.10.2023
- Impfdatum
- 19.10.2023
- Beginn
- 20.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site rash
Pain in extremity
Sleep disorder
Symptomtext
Patient woke up early morning of 10/20/2023 due to pain in her left arm. Area had a rash (redness) in the middle of the upper arm on the left side. Later on she took over the counter Benadryl and 2 Ibuprofen to help with the rash and pain in the arm. She presents today 10/24/2023 with a red area around the middle of the upper arm with pain continuing today. Is better than when it first started.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 21.10.2023
- Impfdatum
- 17.10.2023
- Beginn
- 19.10.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Symptomtext
PATIENT BEGAN TO EXPERIENCE A RASH ALL OVER THE BODY AND ITCHIN ON THURSDAY, OCTOBER 19TH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Breast cancer
- Andere Medikamente
- -
- Allergien
- sulfa, cipro
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 09.10.2023
- Impfdatum
- 07.10.2023
- Beginn
- 07.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Nausea
Pollakiuria
Symptomtext
Frequent urination through the first night and the following morning. Frequency was almost hourly during the night. Also experienced nausea and severe chills.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 09.10.2023
- Impfdatum
- 04.10.2023
- Beginn
- 04.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Arthralgia
Asthenia
Decreased appetite
Diarrhoea
Dizziness
Fatigue
Nausea
Symptomtext
Fatigue, lack of energy, abdominal pain, pain in knee joints, nausea, diarrhea, near fainting, lack of appetite.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Rosuvastatin Multivitamin Vitamin D Loratidine
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 09.10.2023
- Impfdatum
- 05.10.2023
- Beginn
- 05.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Brain fog
Dizziness
Fall
Musculoskeletal disorder
Symptomtext
I don't remember how, or what time it was nor how I got to the floor, but I never experienced fainting, but I felt faint. I was very foggy, almost like unaware of me being on the floor. I am not sure if I fell or was trying to get into my recliner and landed on the floor. I landed on the floor first. I had absolutely no muscle control in my legs and barely in my arms to prop myself up to get into that recliner. As I was on the floor trying to get up, it was almost like I was paralyzed, then after a few mins I was finally able to get into the chair.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- High blood pressure, hypercholesterolemia
- Andere Medikamente
- 12.5 mg of Nepoprololer suctinante, Vitamin D3 2000IU, 1000u D3 and K2, Vitamin A 3000mcg, chewable biotin 5000 mcg, resveratrol 200mg, 1 cranberry concentrate axcel 500 mg, High blood pressure, heart meds
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 05.10.2023
- Impfdatum
- 03.10.2023
- Beginn
- 05.10.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Rash on Chest
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PACs (Premature atrial contractions -- ectopic heartbeats)
- Andere Medikamente
- Flecainide 50 mg Preservision Areds 2 vitamins Aspirin 81 mgs Simvastatin 10 mgs
- Allergien
- -
- Vorherige Impfungen
- Rash after shingles vaccination, but not as red
- Staat
- NH
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 05.10.2023
- Impfdatum
- 03.10.2023
- Beginn
- 05.10.2023
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
resident covered in hives, on left arm, trunk, groin. APRN orders for Prednisone 70 mg one time, oral Benadryl po 25 mg Q 6 hours Diphendydramine HCL Sol 1 time IM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No illnesses
- Vorgeschichte
- spinal Stenosis, Paraplegia, Radiculopathy lumbar region, Neuromuscular Disfunction of bladder, Chronic pulmonary Embolism, HTN, Spina bifida (Lumbar)
- Andere Medikamente
- Oxycodone, tizanidine, Metoprolol, Loratadine, Gabapentin, ASA, APAP
- Allergien
- Sulfa Antibiotics, Ciprofloxacin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 04.10.2023
- Impfdatum
- 02.10.2023
- Beginn
- 02.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Headache
Malaise
Pain
Symptomtext
She got her vaccine, had a headache, low temperature, body aches. She felt like she had COVID. Her arm was not too bad. She took extra strength Tylenol and Ibuprofen. Her temp got up to 100, but was kept down due to taking the Tylenol and Ibuprofen. Tuesday she wasn't as achy but still had a headache and a low temp. Today she is still feeling fine. She did not call her doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High cholesterol.
- Andere Medikamente
- Zocor, Chewable calcium and Vitamin D.
- Allergien
- Penicillin, possibly to bacitracin and band-aides.
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 12.12.2023
- Beginn
- 12.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, Agency, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 28.12.2023
- Impfdatum
- 12.12.2023
- Beginn
- 12.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 28.12.2023
- Impfdatum
- 12.12.2023
- Beginn
- 12.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, Agency, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 12.12.2023
- Beginn
- 12.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 12.12.2023
- Beginn
- 12.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 08.12.2023
- Beginn
- 08.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, Agency, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 08.12.2023
- Beginn
- 08.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, state registry, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 07.12.2023
- Beginn
- 07.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, Agency, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 12.12.2023
- Beginn
- 12.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine Spikevax was given outside of the date of use. The vaccine had been out of the recommedned storage temperature for 7 days. Manufacturer notified advised to not readminister. Patient notified of this event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 28.12.2023
- Impfdatum
- 12.12.2023
- Beginn
- 12.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine Spikevax was given outside of the date of use. The vaccine had been out of the recommedned storage temperature for 7 days. Manufacturer notified advised to not readminister. Patient notified of this event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 11.12.2023
- Beginn
- 11.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine Spikevax was given outside of the date of use. The vaccine had been out of the recommedned storage temperature for 6 days. Manufacturer notified advised to not readminister. Patient notified of this event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 28.12.2023
- Impfdatum
- 11.12.2023
- Beginn
- 11.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine Spikevax was given outside of the date of use. The vaccine had been out of the recommedned storage temperature for 6 days. Manufacturer notified advised to not readminister. Patient notified of this event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 07.12.2023
- Beginn
- 07.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, Agency, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 07.12.2023
- Beginn
- 07.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, Agency, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 11.12.2023
- Beginn
- 11.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine Spikevax was given outside of the date of use. The vaccine had been out of the recommedned storage temperature for 6 days. Manufacturer notified advised to not readminister. Patient notified of this event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 11.12.2023
- Beginn
- 11.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine Spikevax was given outside of the date of use. The vaccine had been out of the recommedned storage temperature for 6 days. Manufacturer notified advised to not readminister. Patient notified of this event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 11.12.2023
- Beginn
- 11.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine Spikevax was given outside of the date of use. The vaccine had been out of the recommedned storage temperature for 6 days. Manufacturer notified advised to not readminister. Patient notified of this event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 11.12.2023
- Beginn
- 11.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine Spikevax was given outside of the date of use. The vaccine had been out of the recommedned storage temperature for 6 days. Manufacturer notified advised to not readminister. Patient notified of this event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 07.12.2023
- Beginn
- 07.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 28.12.2023
- Impfdatum
- 11.12.2023
- Beginn
- 11.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine Spikevax was given outside of the date of use. The vaccine had been out of the recommedned storage temperature for 6 days. Manufacturer notified advised to not readminister. Patient notified of this event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 28.12.2023
- Impfdatum
- 07.12.2023
- Beginn
- 07.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, Agency, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 28.12.2023
- Impfdatum
- 11.12.2023
- Beginn
- 11.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine Spikevax was given outside of the date of use. The vaccine had been out of the recommedned storage temperature for 6 days. Manufacturer notified advised to not readminister. Patient notified of this event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 06.12.2023
- Beginn
- 06.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, Agency, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 06.12.2023
- Beginn
- 06.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, Agency, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 06.12.2023
- Beginn
- 06.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 06.12.2023
- Beginn
- 06.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 06.12.2023
- Beginn
- 06.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, Agency, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 28.12.2023
- Impfdatum
- 06.12.2023
- Beginn
- 06.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 06.12.2023
- Beginn
- 06.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The COVID vaccine given in December was outside of the date of use. The manufacturer was contacted and recommended not re-administration. PCP, Agency, risk management has been notified of the event. Staff training and education has been completed to avoid reoccurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 27.12.2023
- Impfdatum
- 11.12.2023
- Beginn
- 11.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine was given outside of date of use. The vaccine had been out of the recommended storage temperatur of 6 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 27.12.2023
- Impfdatum
- 06.12.2023
- Beginn
- 06.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Spikevax vaccine was given out of the use of date. Vaccine was given 1 day outside of recommended usage.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 27.12.2023
- Impfdatum
- 08.12.2023
- Beginn
- 12.12.2023
- Tage bis Beginn
- 4,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine Spikevax was given outside of the date of use. The vaccine had been out of the recommended storage temperature for 31 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 27.12.2023
- Impfdatum
- 08.12.2023
- Beginn
- 08.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine was given outside of date of use. The vaccine had been out of the recommended storage temperature for 31 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 27.12.2023
- Impfdatum
- 06.12.2023
- Beginn
- 06.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine Spikevax was given outside of the date of use. It had been out of the freezer 31 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 27.12.2023
- Impfdatum
- 01.12.2023
- Beginn
- 27.12.2023
- Tage bis Beginn
- 26,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Administered a 2nd time on 12/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Hydroxyzine, melatonin
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 20.11.2023
- Impfdatum
- 09.10.2023
- Beginn
- 19.11.2023
- Tage bis Beginn
- 41,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
hospitalized with COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- OSA on CPAP, pAF, CVA s/p LHC w/o intervention 10/22/23, renal stenosis, RCA stenosis s/p CEA.
- Andere Medikamente
- unknown
- Allergien
- alfuzosin HCl, Statins, amoxicillin, gemfibrozil, niacin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 08.11.2023
- Impfdatum
- 01.11.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Device issue
No adverse event
Symptomtext
The plunger component of the syringe was completely stuck. He was unable to push the vaccine through the needle to administer to the patient; No adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of DEVICE ISSUE (The plunger component of the syringe was completely stuck. He was unable to push the vaccine through the needle to administer to the patient) and NO ADVERSE EVENT (No adverse event) in a 59-year-old female patient who received mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) (batch no. 3032218) for COVID-19 prophylaxis. The suspect product included Pre-filled Syringe injection (batch no. 3032218) for COVID-19 prophylaxis. No Medical History information was reported. On 01-Nov-2023, the patient received dose of mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) (unknown route) 1 dosage form. On an unknown date, the patient started Pre-filled Syringe (unknown route) at an unspecified dose. On an unknown date, the patient experienced DEVICE ISSUE (The plunger component of the syringe was completely stuck. He was unable to push the vaccine through the needle to administer to the patient) and NO ADVERSE EVENT (No adverse event). At the time of the report, DEVICE ISSUE (The plunger component of the syringe was completely stuck. He was unable to push the vaccine through the needle to administer to the patient) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for DEVICE ISSUE (The plunger component of the syringe was completely stuck. He was unable to push the vaccine through the needle to administer to the patient). For Pre-filled Syringe, the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for DEVICE ISSUE (The plunger component of the syringe was completely stuck. He was unable to push the vaccine through the needle to administer to the patient). No concomitant medications were provided. The pharmacist technician was calling about defective dose of Spikevax PFS (with blister pack). Upon administering the dose to the patient on 1Nov2023, the plunger component of the syringe was completely stuck. He was unable to push the vaccine through the needle to administer to the patient. He had to open a new one. The HCP confirmed that he used a different syringe with same lot number (3032218) to administer the dose to the patient. He did not use any of the dose that was in the defective syringe, but he did inject the patient with the needle. He was requesting a replacement for the defective syringe. The Device problem code for Spikevax syringe include FDA code, agency code which include Defective Device. The device was malfunctioned, and the malfunction type. No treatment medications were provided. Most recent FOLLOW-UP information incorporated above includes: On 01-Nov-2023: Live Follow up received contains PQC report that includes reference number added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Device issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 24.10.2023
- Impfdatum
- 24.10.2023
- Beginn
- 24.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Wrong product administered
Symptomtext
Incorrect vaccination given. Patient did not have any symptoms. correct vaccine was given in opposite arm as outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hyperlipidemia, Hypertension, Obesity, Overweight, Erectile disorder die to medical condition in male, History of bladder carcinoma, Primary prostate cancer, Lung nodule, Obstructive sleep apnea, Rosacea, Acrochordon, Actinic Keratosis, Seborrheic dermastitis, History of nicotine dependence
- Andere Medikamente
- -Lisinopril, Sildenafil, Pravastatin, Voltaren, Prevagen
- Allergien
- Penicillins
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 11.10.2023
- Impfdatum
- 29.09.2023
- Beginn
- 05.10.2023
- Tage bis Beginn
- 6,0
- Dosis
- 7+
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Symptomtext
Complete loss of taste
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ageusia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, under control with medication Pre-diabetes, under control with medication
- Andere Medikamente
- -Losartan HCTZ 100/25mg once daily; -Bystolic 2.5mg once daily; (nebivolol): -Metformin HCL 500mg daily: -Multi for Men over 50 -Fiber -D3/K2
- Allergien
- None
- Vorherige Impfungen
- -