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From the 9/10/2021 release of VAERS data:

This is VAERS ID 1496245

Case Details

VAERS ID: 1496245 (history)  
Form: Version 2.0  
Sex: Female  
Location: Foreign  
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-07-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route

Administered by: Other       Purchased by: ?
Symptoms: Blood test, Inappropriate schedule of product administration, Lymphadenopathy, Maternal exposure timing unspecified, SARS-CoV-2 test, Scan, Tremor, Vitamin D decreased
SMQs:, Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnancy
Diagnostic Lab Data: Test Name: blood test; Result Unstructured Data: Test Result:low Vitamin D; Test Name: COVID-19 virus test; Test Result: Negative ; Test Name: SPECT Scan; Result Unstructured Data: Test Result:nothing to indicate another explanation; Comments: nothing to indicate another explanation for the enlargement of the lymph nodes, other than the vaccine
CDC Split Type: GBPFIZER INC2021864057

Write-up: low vitamin; an exposure during pregnancy; dose 1 on 19May2021, dose 2 on 03Jul2021; Shaking; Enlarged lymph nodes (excl infective); This is a spontaneous report from a contactable consumer or other non hcp received from a regulatory authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202107062041167410-GPEG1. Safety report unique identifier GB-MHRA-ADR 25607200. A 37-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 19May2021 (Batch/Lot number was not reported) as single dose, dose 2 via an unspecified route of administration on 03Jul2021 (Batch/Lot number was not reported) as single dose, for COVID-19 immunization. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Medical history included pregnancy from an unknown date and unknown if ongoing. The patient''s concomitant medications were not reported. The patient experienced low vitamin on an unspecified date with outcome of recovering, enlarged lymph nodes (excl infective) on 03Jun2021 with outcome of not recovered, shaking on 06Jul2021 with outcome of not recovered. About a week or so after the 1st dose, the patient noticed a lymph node under left armpit was enlarged. After another week or so as the left armpit enlarged node reduced in size, a new one developed on the right. They alternated between left and right armpit till about 4 weeks after 1st dose. The patient had just had a SPECT Scan about 3 months prior and there was nothing to indicate another explanation for the enlargement of the lymph nodes, other than the vaccine. The patient also had a blood test about 3 weeks after the 1st dose and nothing except low Vitamin D. The patient just had the 2nd dose and nodes on the left are enlarging now. The patient also experienced and was still experiencing shaking after the vaccine, most especially arms and hands. The shaking lasted over a week after the 1st dose and its been 2 days now with the 2nd dose. No medication was taken for any of these reactions. Adverse reaction did not occur as a result of an exposure during pregnancy. The patient underwent lab tests and procedures which included COVID-19 virus test on an unspecified date: No - Negative COVID-19 test. Patient has not tested positive for COVID-19 since having the vaccine. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

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