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From the 11/19/2021 release of VAERS data:

Found 2,686 cases where Vaccine is COVID19 and Symptom is Aborted pregnancy or Abortion or Abortion complete or Abortion early or Abortion incomplete or Abortion induced or Abortion late or Abortion missed or Abortion of ectopic pregnancy or Abortion spontaneous or Abortion spontaneous complete or Abortion spontaneous incomplete or Foetal cardiac arrest or Foetal death or Premature baby death or Premature delivery or Stillbirth

Government Disclaimer on use of this data



Case Details (Sorted by Onset Date)

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VAERS ID: 1164134 (history)  
Form: Version 2.0  
Age: 23.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-03-15
Onset:2021-03-15
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 002B21A / 1 LA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Asthenia, Exposure during pregnancy, Fatigue
SMQs:, Guillain-Barre syndrome (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: Allergic to amoxicillin
Diagnostic Lab Data:
CDC Split Type:

Write-up: The day I got my shot, by 5:30pm I was to tired and week to even move. I didn?t know I was pregnant at the time because it was so early. 7 days later I found out I was pregnant, 4 weeks along. And three days later on 3/25 I miscarried.


VAERS ID: 1185268 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-02-09
Onset:2021-03-15
   Days after vaccination:34
Submitted: 0000-00-00
Entered: 2021-04-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 041L20A / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Foetal exposure during pregnancy, Foetal heart rate abnormal, Ultrasound scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: pre-natal vitamin
Current Illness: no
Preexisting Conditions: no
Allergies: no
Diagnostic Lab Data: Ultrasound - 3/15/2021 - Birth and Women''s health center
CDC Split Type: vsafe

Write-up: 3/15/2021 - Went to my midwife for my first prenatal visit and that''s where I learned there was no heartbeat. 4 weeks along at the time of the vaccine and the heartbeat ended at 8 weeks along. This was my third pregnancy - and my first miscarriage. Estimated date of delivery was in October.


VAERS ID: 1361967 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: New York  
Vaccinated:2021-03-07
Onset:2021-03-15
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-05-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1805022 / 1 RA / SYR

Administered by: School       Purchased by: ?
Symptoms: Abortion spontaneous, Chills, Exposure during pregnancy, Feeling abnormal, Foetal death, Illness, Pain, Pyrexia, Ultrasound foetal abnormal
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: None
Preexisting Conditions: Asthma
Allergies: Allergy to morphine
Diagnostic Lab Data:
CDC Split Type:

Write-up: The day after I received the vaccine I was very ill. I had a fever of 103 for most of 24 hours after the shot. I had body aches and chills and just felt generally horrible. I was 8 weeks pregnant with twins at the time of the vaccine. 3 days after the vaccine I had an ultrasound which showed a large blood vessel between the twins. On March 23rd I had another ultrasound and neither of one of my twins had a heartbeat. From the measurements they could tell that I lost one twin the week of March 15th and I lost the other one the week of March 22nd.


VAERS ID: 1462103 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-19
Onset:2021-03-15
   Days after vaccination:55
Submitted: 0000-00-00
Entered: 2021-07-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 AR / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Foetal death, Human chorionic gonadotropin, Ultrasound scan abnormal
SMQs:, Malignancy related therapeutic and diagnostic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

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: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Initial pregnancy labs remarkable for low HCG followed by ultrasound evidence of fetal demise
CDC Split Type:

Write-up: Miscarriage at 8 weeks gestation in two consecutive pregnancies in March 2021 and June 2021


VAERS ID: 1162347 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-26
Onset:2021-03-15
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-04-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

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: Disease risk factor
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLPFIZER INC2021302444

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer or other non hcp downloaded from the Regulatory Authority-WEB NL-LRB-00478034, Safety Report Unique Identifier NL-LRB-00480445, received from Regulatory Authority. A 24-year-old female pregnant patient received bnt162b2 (COMIRNATY), dose 2 via an unspecified route of administration on 26Feb2021 (Batch/Lot Number: unknown) as SINGLE DOSE, dose 1 via an unspecified route of administration on 29Jan2021 (Batch/Lot Number: unknown) as SINGLE DOSE for covid-19 immunisation. Medical history included disease risk factor from an unknown date. No past drug therapy with BioNTech / Pfizer vaccine (Comirnaty). No previous COVID-19 infection. The patient experienced miscarriage reported as Embryo lost (other medically important condition) on 15Mar2021 following administration of covid-19 vaccine Pfizer Injectable solution. The miscarriage occurred at gestational age 4 weeks and 4 days, 17 days after the second covid-19 vaccination. At the second vaccination patient did not know that she was pregnant. COVID-19 vaccine exposure during pregnancy week: 0, 2nd vaccination at 1 to 2 weeks gestation. Outcome of the event was unknown. No follow-up attempts are possible, information on batch number cannot be obtained.


VAERS ID: 1170710 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-03
Onset:2021-03-15
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

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: FOLIC ACID
Current Illness: Pregnancy (Patient no longer pregnant at the time of reporting.)
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021313210

Write-up: Maternal exposure during pregnancy/exposed to the medicine first-trimester (1-12 weeks); Miscarriage; This is a spontaneous report from the United Kingdom''s Medicines and Healthcare products Regulatory Agency (UK-MHRA). The regulatory authority report number is GB-MHRA-WEBCOVID-202103212124247400, Safety Report GB-MHRA-ADR 24993697. A contactable consumer reported that a 29-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: unknown) via an unspecified route of administration, on 03Mar2021, at a single dose for COVID-19 immunisation. Medical history included abortion spontaneous and pregnancy (no longer pregnant at the time of reporting). Patient has not had symptoms associated with COVID-19. Patient has not had a COVID-19 test. Patient is not enrolled in clinical trial Patient is not currently breastfeeding. Concomitant medication included folic acid for folic acid supplementation. The patient previously received first dose of BNT162B2 for COVID-19 immunisation. Patient received COVID vaccine in early pregnancy as frontline healthcare worker. Patient was exposed to the medicine first-trimester (1-12 weeks) (maternal exposure during pregnancy). On 15Mar2021, 2 weeks later, patient had miscarriage. The events were considered serious due to other medically important condition. Outcome of the event miscarriage was recovering. 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.


VAERS ID: 1746817 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-07
Onset:2021-03-15
   Days after vaccination:67
Submitted: 0000-00-00
Entered: 2021-09-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Investigation, SARS-CoV-2 test
SMQs:, Termination of pregnancy and risk of abortion (narrow), 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: Pfizer, Inc. EUA 027034
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Metastatic neoplasm (Pre cancer cells removed 5/6 years ago); Pregnancy (Patient no longer pregnant at the time of reporting.); Total hip replacement
Allergies:
Diagnostic Lab Data: Test Name: scans or investigations; Result Unstructured Data: Test Result:Missed miscarriage; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC202101225236

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer (patient). This report is received from the regulatory authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202109162316005290-ODXLD. Safety Report Unique Identifier: GB-MHRA-ADR 25956576. A 35-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, lot number was not reported), via an unspecified route of administration on 07Jan2021 as first dose, single for COVID-19 immunisation. Medical history included total hip replacement from unspecified date in 2018, metastatic neoplasm (Pre cancer cells removed 5/6 years ago), and non-ongoing pregnancy (patient no longer pregnant at the time of reporting). Patient has not had symptoms associated with COVID-19. Patient is not currently breastfeeding. Concomitant medication included folic acid for folic acid supplementation. The patient experienced miscarriage on 15Mar2021 with outcome of unknown. The mother reported she became pregnant while taking bnt162b2. The patient underwent lab tests and procedures which included scans which showed missed miscarriage on an un specified date; covid-19 virus test: no - negative covid-19 test on unspecified date. Patient has not tested positive for COVID-19 since having the vaccine. Patient is not enrolled in clinical trial. The patient was unsure if the medicine have an adverse effect on any aspect of the pregnancy. Patient was exposed to the medicine first-trimester (1-12 weeks). No follow-up attempts are possible; information about batch/lot number cannot be obtained. No further information is expected.


VAERS ID: 1138287 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Tennessee  
Vaccinated:2021-03-06
Onset:2021-03-16
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-03-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6204 / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal death, Haematocrit decreased, Haemoglobin decreased, Induced labour, Mean cell haemoglobin concentration decreased, Mean cell haemoglobin decreased, Mean cell volume normal, Mean platelet volume increased, Nucleated red cells, Platelet count normal, Red blood cell count normal, Red cell distribution width increased, Stillbirth, White blood cell count normal
SMQs:, Haematopoietic erythropenia (broad), Haemorrhage laboratory terms (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

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? Yes, 3 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: vitamin code prenatals OTC Omeprazole- PRN
Current Illness: none
Preexisting Conditions: left hip arthritis
Allergies: None
Diagnostic Lab Data: blood test done 03/19/2021: white blood cell= 7.9 red blood cell= 4.33 hemoglobin= 10.0gm/dL hematocrit%= 35% mean cell volume= 80 fL mean cell hemoglobin = 23.1 pg mean cell hemoglobin concentration= 28.8 gm/dL RDW CV= 16.3% Platelet= 267 mean platelet volume= 10.5 fL nucleated RBC =0 nucleated RBC Abs = 0
CDC Split Type:

Write-up: Pregnancy- about 27 weeks- estimated delivery= 06/19/2021 On 03/17/2021 around 9pm cst i actually noticed very little to no movement went to labor triage on 03/18/2021 around 9am- baby has demised and on 03/19 /2021 i was induced and 03/20/2021 a 11am cst. baby born stillbirth at 2.05lbs and 14.5 inches long


VAERS ID: 1211763 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-07
Onset:2021-03-16
   Days after vaccination:68
Submitted: 0000-00-00
Entered: 2021-04-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1484 / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion, Inappropriate schedule of product administration
SMQs:, Termination of pregnancy and risk of abortion (narrow), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: ITPFIZER INC2021342789

Write-up: Internal abortion. Gestational age 11 + 3, ultrasound age 8 + 3. I had received the first dose of the Pfizer-Biontech Covid vaccine on January 7, 2021. I gave up the second dose due to pregnancy; gave up the second dose due to pregnancy; This is a spontaneous report from a contactable consumer (patient) downloaded from the WEB, regulatory authority number IT-MINISAL02-705468. A 33-year-old female patient received bnt162b2 (COMIRNATY), dose 1 intramuscular on 07Jan2021 11:20 (Lot Number: EL1484) as 0.3 mL, single for covid-19 immunisation. The patient medical history was not reported. The patient''s concomitant medications were not reported. On 27Jan2021, (the day before the second dose), the patient discovered she was pregnant. On 16Mar2021, abortion. Actions taken: Hysterosuction and revision of the uterine cavity carried out on 18Mar2021. Impact on quality of life (10/10). The patient received the vaccine as an employee of a health company. The patient reported that she had a previous pregnancy, completed without problems, on 31Dec2018 and that she had not taken estrogen-progestogen therapies, not even previously. The patient experienced internal abortion on 16Mar2021. Gestational age 11 + 3, ultrasound age 8 + 3. The mother was 11 weeks pregnant at the onset of the event. The mother was due to deliver on 03Oct2021. The patient gave up the second dose due to pregnancy. The patient was hospitalized due to the event. The patient has recovered from the event. Sender''s comment: The report was reported as severe or permanent severe disability. It was changed to hospitalization as the abortion led to an intervention in the hospital. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1234968 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-16
Onset:2021-03-16
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Ultrasound foetal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

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:
Allergies:
Diagnostic Lab Data: Test Name: ultrasound measurements; Result Unstructured Data: Test Result:the size of my baby corresponds to week 7
CDC Split Type: ILPFIZER INC2021379858

Write-up: miscarriage after Covid-19 vaccination/at week 7+1, we believe he died a few days after; The patient did the first vaccination on 16Mar2021 while patient was pregnant for 7+3 weeks.; This is a spontaneous report from a contactable consumer (patient). A 42-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 16Mar2021 as single dose for covid-19 immunisation. The patient medical history was not reported. The patient''s concomitant medications were not reported. The patient did the first vaccination on 16Mar2021 while patient was pregnant for 7+3 weeks. on 05Apr2021, the patient found out baby has no pulse. According to ultrasound measurements, the size of baby corresponds to week 7. Since baby had a pulse 2 days before the vaccination, at week 7+1, they believe baby died a few days after, meaning after the vaccination. Patient know that miscarriages in the first trimester are very common and especially after the age of 40, and that it may very well have nothing to do with the vaccine other than a coincidence but it seemed important to patient to update. The outcome of events was unknown. Information on the lot/batch number has been requested.; Sender''s Comments: Considering a plausible temporal association between the reported events of Spontaneous Abortion and the suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1268488 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-16
Onset:2021-03-16
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER1741 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Inappropriate schedule of product administration, Intermenstrual bleeding, Maternal exposure during pregnancy, Off label use, Scan
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Medication errors (narrow)

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: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid supplementation
Allergies:
Diagnostic Lab Data: Test Name: scan; Result Unstructured Data: Test Result:viable pregnancy; Comments: scan at 6 weeks
CDC Split Type: GBPFIZER INC2021405272

Write-up: light bleeding in early pregnancy; Maternal exposure during pregnancy; Miscarriage; first dose of bnt162b2 on 12Jan2021; second dose of bnt162b2 on 16Mar2021; first dose of bnt162b2 on 12Jan2021; second dose of bnt162b2 on 16Mar2021; This is a spontaneous report from a contactable consumer received from the Regulatory authority report number is GB-MHRA-WEBCOVID- 202104121308456100, Safety Report Unique Identifier is GB-MHRA-ADR 25125239. A 32-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: ER1741, Expiry date not reported), via an unspecified route of administration at single dose on 16Mar2021 for COVID-19 immunization. Medical history included vitamin supplementation (Folic acid supplementation) from an unknown date and unknown if ongoing. Patient had not had symptoms associated with COVID-19. Patient had not had a COVID-19 test. Patient was pregnant at vaccination, but no longer pregnant at the time of reporting. Patient was not enrolled in clinical trial. Patient was not currently breastfeeding. Concomitant medication included folic acid taken for vitamin supplementation (folic acid supplementation), start and stop date were not reported. Historical vaccine included first dose of bnt162b2 (lot number: EE8493) on 12Jan2021 for COVID-19 immunization. The patient experienced light bleeding in early pregnancy on an unspecified date with outcome of unknown, maternal exposure during pregnancy on an unspecified date with outcome of unknown, and miscarriage on 09Apr2021 with outcome of recovering. The patient underwent lab tests and procedures which included scan: viable pregnancy on scan at 6 weeks on an unspecified date. The events were reported as serious, medically significant. Narrative case summary and further information: Case narrative: Miscarriage on 9Apr2021, approx 7-8 weeks problems. I do not think the vaccine cause the miscarriage. Patient had not tested positive for COVID-19 since having the vaccine. Patient was exposed to the medicine first-trimester (1-12 weeks). Details of scans or investigations: Light bleeding in early pregnancy, scan at 6 weeks showed viable pregnancy; vaccine administered week 5. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1324858 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-02
Onset:2021-03-16
   Days after vaccination:42
Submitted: 0000-00-00
Entered: 2021-05-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, SARS-CoV-2 test
SMQs:, Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Lactation decreased; Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021493073

Write-up: Early miscarriage; This is a spontaneous report from a contactable consumer. This is a report received from the Regulatory Agency. Regulatory authority report number GB-MHRA-WEBCOVID-202104301233076550-XXUY5, Safety Report Unique Identifier GB-MHRA-ADR 25224189. A 30-year-old female patient received BNT162B2 (BNT162B2, lot/batch number and expiry date were not reported), via an unspecified route of administration on 02Feb2021 (also reported as 20Feb2020) as first dose, single for COVID-19 immunisation. Medical history included pregnancy (no longer pregnant at the time of reporting) and suppressed lactation. Patient has not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. Concomitant medication included folic acid for vitamin supplementation, start and stop date were not reported. The patient experienced early miscarriage/early miscarriage at 4 weeks (reported as serious medically significant) on 16Mar2021. It was further reported that she was exposed to the medicine before pregnancy. The patient underwent laboratory test included Sars-cov-2 test: No - Negative COVID-19 test on unknown date. The outcome of event was recovered on 17Mar2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained


VAERS ID: 1109612 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-02-10
Onset:2021-03-17
   Days after vaccination:35
Submitted: 0000-00-00
Entered: 2021-03-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 UN / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion missed, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamins
Current Illness: none
Preexisting Conditions: none
Allergies: no known allergies
Diagnostic Lab Data:
CDC Split Type:

Write-up: Missed abortion noted about one month after 1st COVID vaccination Patient was supposed to be around 11weeks pregnant. She had a prior ultrasound with a single live intrauterine pregnancy on Feb 24, 2021. EDD was October 3rd, 2021. Fetus with no heart tones noted on March 17th, 2021. Fetus measuring about 8 weeks pregnant patient only noted elevated temperature after COVID vaccination


VAERS ID: 1117082 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: South Carolina  
Vaccinated:2021-01-27
Onset:2021-03-17
   Days after vaccination:49
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3249 / 1 - / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6198 / 2 - / IM

Administered by: Private       Purchased by: ?
Symptoms: Caesarean section, Exposure during pregnancy, Foetal biophysical profile score abnormal, Premature delivery, Ultrasound antenatal screen
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow)

Life Threatening? Yes
Birth Defect? Yes
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: prenatal vitamins, pepcid
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Ultrasound prenatally and multiple ultrasounds of my infant, kidneys, abdominal, brain and heart. Multiple CBC''s and coagulation profiles
CDC Split Type:

Write-up: Pregnancy with EDC of 5/7/2021. On 3/17/2021 infant was not moving as expected, went to hospital and emergency c-section performed due to failure of BPP score. Score was 2. Infant delivered @ 32 week. Wt. was 4#4 oz. Infant had blood in urine. After numerous studies my baby was found to have thrombosis in the intrahepatic IVC. Treatment has started.


VAERS ID: 1128192 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Oklahoma  
Vaccinated:2021-01-19
Onset:2021-03-17
   Days after vaccination:57
Submitted: 0000-00-00
Entered: 2021-03-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Uterine dilation and curettage
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Lupus
Allergies:
Diagnostic Lab Data: D and C procedure
CDC Split Type:

Write-up: Pregnant with second child at first and second dose of the covid vaccine. Due date was 10/15/2011. I experienced a miscarriage at 9 weeks pregnant on 3/17/2021.


VAERS ID: 1163402 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2021-03-16
Onset:2021-03-17
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-04-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / 1 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound foetal
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Levothyroxine .75mg
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: Cinnamon
Diagnostic Lab Data: Ultrasound - 03/31/2021 Showed baby stopped growing around 03/17/21
CDC Split Type:

Write-up: Miscarriage - due date was 10/16/2021


VAERS ID: 1172727 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Nevada  
Vaccinated:2021-03-12
Onset:2021-03-17
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 024M20A / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Laboratory test
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vit, Ginger Pills
Current Illness: Chemotherapy taken in 01/21
Preexisting Conditions: Tenacious?
Allergies: Iodine, Contrast, Shellfish, Allergy,Urticaria
Diagnostic Lab Data: Blood test
CDC Split Type: vsafe

Write-up: The Monday I had blood test it was normal and progesterone was little low. I started miscarrying on Wed on 3/27. My estimated date of delivery would have been mid Nov. 2021.


VAERS ID: 1205793 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Male  
Location: Alaska  
Vaccinated:2021-02-01
Onset:2021-03-17
   Days after vaccination:44
Submitted: 0000-00-00
Entered: 2021-04-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 AR / IM

Administered by: Military       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure before pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Fish oil, multivitamin, vitamin d, seroquel, luenesta, omprazole, celexa
Current Illness: None
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Wife got pregnant in between the 2 shots. She had a miscarriage.


VAERS ID: 1290907 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-02-11
Onset:2021-03-17
   Days after vaccination:34
Submitted: 0000-00-00
Entered: 2021-05-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 004M20A / 2 RA / IM

Administered by: Senior Living       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Pregnancy
SMQs:, Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Na
Current Illness: None. Miscarried March 17th 2021. Not even 4 weeks after 2nd Covid-19 vaccine. No history of miscarriage.
Preexisting Conditions: None
Allergies: Bananas
Diagnostic Lab Data: Several blood test Available.
CDC Split Type:

Write-up: History of 3 viable pregnancies, live births. No miscarriages. 2nd vaccine 2/11/21, confirmed pregnancy 3/10/21, confirmed miscarriage 3/17/21.


VAERS ID: 1361973 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-03-11
Onset:2021-03-17
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-05-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 027A21A / 2 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abdominal pain, Abortion missed, Exposure during pregnancy, Haemorrhage, Ultrasound scan
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient asked how to report a missed abortion (miscarriage) after the second dose of the Moderna vaccine since she was told by doctors to report it. Patient had a positive pregnancy test on 3/14/21 after receiving the second dose of Moderna on 3/11/21 but did not know prior to receiving the second dose. Patient stated that it was determined she was 6 weeks pregnant 6 days after the second shot. On 4/1/2021 patient had abdominal pain and bleeding so went to the emergency room and an ultrasound was performed. It was determined that the missed abortion occurred when the baby was at 6 weeks. After several doctor visits, the patient was advised to report this and that is why this was brought to our attention. She simply asked how to report this and then I asked her some questions and gathered information. She was okay and sounded fine.


VAERS ID: 1234372 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-25
Onset:2021-03-17
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-04-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP9598 / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
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: Psoriatic arthropathy (She was treated with METHOTREXATE then HUMIRA stopped on 19Apr2020)
Allergies:
Diagnostic Lab Data:
CDC Split Type: FRPFIZER INC2021369668

Write-up: Early miscarriage; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority-WEB, regulatory authority number FR-AFSSAPS-MA20210991. This physician reported information for both mother and fetus/baby. This is the maternal report. A 34-year-old female patient of an unspecified age received bnt162b2 (COMIRNATY) (at 34 years of age), dose 1 intramuscular on 25Feb2021 (Batch/Lot Number: EP9598) as a single dose for COVID-19 immunisation. Medical history included psoriatic arthropathy in which she was treated with methotrexate then HUMIRA. The patient''s concomitant medications were not reported. The patient previously took methotrexate then HUMIRA for psoriatic arthropathy which stopped on 19Apr2020. The patient had no history of Covid-19 infection. The patient experienced early miscarriage on 17Mar2021. The outcome of the events was recovered. The mother reported she became pregnant while taking bnt162b2. The mother was 10 Weeks pregnant at the onset of the event. Further ADR description stated that the 34-year-old patient who had stopped pregnancy after the first dose of COMIRNATY. The patient was vaccinated on 25Feb2021 at 25 days of amenorrhea. On 17Mar2021, the embryo measured only 4 mm while its gestational age should correspond to a size of 10 mm. In front of the premature stop of growth, termination of the pregnancy on the same day. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : FR-PFIZER INC-2021415432 fetus case


VAERS ID: 1265095 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-18
Onset:2021-03-17
   Days after vaccination:27
Submitted: 0000-00-00
Entered: 2021-04-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, SARS-CoV-2 test
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FIASP; FOLIC ACID; TRESIBA
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Clinical trial participant (Viruswatch); Diabetic; Pregnancy (Patient no longer pregnant at the time of reporting. three previous full term pregnancies); Comments: Type 1 diabetic Patient has not had symptoms associated with COVID-19 Patient is not currently breastfeeding
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021399366

Write-up: Maternal exposure during pregnancy; Miscarriage; This is a spontaneous report from a contactable Consumer received from the Medicines Healthcare Products Regulatory Agency (MHRA). Regulatory authority report number GB-MHRA-WEBCOVID-202104111758341690. A 35-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration at single dose on 18Feb2021 (Lot number was not reported) for COVID-19 immunization. Medical history included pregnancy (Patient no longer pregnant at the time of reporting. three previous full-term pregnancies), clinical trial participant (Virus watch), Type 1 diabetic. Patient has not had symptoms associated with COVID-19. Patient is not currently breastfeeding. Concomitant medication included insulin aspart (FIASP); folic acid at 400 ug taken for vitamin supplementation; insulin degludec (TRESIBA). The patient experienced maternal exposure during pregnancy on an unspecified date, miscarriage on 17Mar2021. Have had three previous full term pregnancies and no previous miscarriages. Miscarriage happened at around 6 weeks. Patient has not tested positive for COVID-19 since having the vaccine. Did the medicine have an adverse effect on any aspect of the pregnancy: Unsure. Patient was exposed to the medicine Before pregnancy. The patient underwent lab tests and procedures which included COVID-19 test: negative on No - Negative COVID-19 test. For event, maternal exposure during pregnancy outcome was unknown, and for miscarriage, outcome was recovered on an unspecified date in 2021. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1285068 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-17
Onset:2021-03-17
   Days after vaccination:59
Submitted: 0000-00-00
Entered: 2021-05-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Foetal death, Thrombosis, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Thrombophlebitis (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021294275

Write-up: miscarriage; blood clot causing the fetus to suffocate; A week or so later, the patient found out that she was pregnant, she was probably 3-4 weeks along then.; she began bleeding quite light then clots appeared; she began bleeding quite light then clots appeared; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date were not provided), via an unspecified route of administration on 17Jan2021 at single dose for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. The patient worked as a caregiver and was given the COVID vaccine on the 17Jan2021. A week or so later, the patient found out that she was pregnant, she was probably 3-4 weeks along then. She was very happy and took every precaution possible. Then she began bleeding quite light then clots appeared on an unspecified date in 2021. The patient went to the hospital on an unspecified date in 2021 but has been told it was too late; she suffered a miscarriage on 17Mar2021 which the physician attributed to blood clot causing the fetus to suffocate. The physician believed the blood clot may have been caused by her receiving the vaccine in the early stages of the pregnancy. The reporter stated that they would like to try again but was concerned that it will happen again. The reporter also queried on how long they should wait to try for a baby, if the patient had the booster. They were referred to speak with their physician on when they should consider attempting to conceive again. The patient wanted to speak with someone at Pfizer to see if the company would have any additional recommendations on when they should attempt to become pregnant again. The outcome of the events was unknown. Information on the lot/batch number has been requested.


VAERS ID: 1447635 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-17
Onset:2021-03-17
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ET3620 / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Anembryonic gestation, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

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:
Allergies:
Diagnostic Lab Data:
CDC Split Type: FRPFIZER INC2021730395

Write-up: Miscarriage; Blighted ovum; drug exposure during pregnancy; This is a spontaneous report from a contactable physician downloaded from the WEB FR-AFSSAPS-PA20210978. This physician reported information for both mother and fetus/baby. A 26-years-old female patient received bnt162b2 (COMIRNATY solution for injection, Batch/Lot number: ET3620), via intramuscular route of administration on 17Mar2021 as dose number unknown, 0.3mL single for COVID-19 immunisation. The medical history and concomitant medications of the patient were not reported. The patient was pregnant at the time of vaccination. The last menstrual period of the patient was 25Feb2021. The patient was pregnant on 11Mar2021. The Obstetrical history was not recorded. It was reported that Clear egg (blighted ovum) was detected on 30Apr2021 and the patient had a haemorrhagic miscarriage in mid May2021 on an unknown date. She reported she became pregnant while taking bnt162b2. She was due to deliver on 30Dec2021. The patient recovered from the events on an unspecified date in 2021. NB: Imputation made without prejudice to the elepreganrments of investigation which could be carried out within the framework of legal or amicable compensation procedures. No follow-up attempts possible. No further information expected.


VAERS ID: 1114093 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-03-16
Onset:2021-03-18
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH I / 1 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

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:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage


VAERS ID: 1254933 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-03-18
Onset:2021-03-18
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6204 / 1 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: LEXAPRO
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Anxiety
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021387492

Write-up: spotting vaginally; miscarriage; Following the vaccine on 18Mar; This is a spontaneous report from a contactable consumer (patient). A pregnant 31-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in left arm on 18Mar2021 at 17:00 (at the age of 31 years old) (Lot Number: EN6204, unknown expiration) as a single dose for COVID-19 immunisation. Medical history included anxiety. No known allergies. Concomitant medications included escitalopram oxalate (LEXAPRO) and unspecified prenatal vitamins. The patient reported that following the vaccine on 18Mar2021 at 23:00 (11:00 pm), she began spotting vaginally which persisted for two weeks and resulted in a miscarriage at 7 weeks pregnant. The patient is pregnant on 04Jan2021. The mother was supposed to deliver on 19Nov2021. The events resulted in doctor or other healthcare professional office/clinic visit. The patient did not received treatment for the events. The patient has no COVID prior to vaccination and was not tested for COVID post vaccination. The patient did not have other vaccine in four weeks. The patient is recovering from the events. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1258913 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-01-13
Onset:2021-03-18
   Days after vaccination:64
Submitted: 0000-00-00
Entered: 2021-04-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3248 / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion missed, Abortion spontaneous, Pregnancy
SMQs:, Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins, vitamin D, calcium
Current Illness:
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: I had a missed miscarriage and had to take mifeprex and misoprostol in order to start the miscarriage process.
CDC Split Type:

Write-up: I become pregnant within 30 days of my 2nd vaccine (last menstrual period (LMP) was February 3rd and I ovulated around February 18th). I then miscarried at 6 weeks and 1 day (3/18/21). I found out I miscarried at 9 weeks and 2 days (4/9/21), but I had a "missed miscarriage" and the baby stopped growing with no heartbeat at 6 weeks and 1 day (3/18/21). My due date would have been November 10th 2021.


VAERS ID: 1410691 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Nevada  
Vaccinated:2021-03-18
Onset:2021-03-18
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / 1 LA / SYR

Administered by: Other       Purchased by: ?
Symptoms: Arthralgia, Cough, Dizziness, Exposure during pregnancy, Foetal death, Head discomfort, Headache, Hypertension, Illness, Joint range of motion decreased, Muscle tightness, Musculoskeletal stiffness, Pain, SARS-CoV-2 test, Secretion discharge
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Hypertension (narrow), Vestibular disorders (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: None
Preexisting Conditions: I had high blood pressure during pregnancy before
Allergies: Nothing severe
Diagnostic Lab Data: None
CDC Split Type: vsafe

Write-up: The day I got the vaccine I noticed a lot of muscle stiffness and joint pain especially in the shoulder, my ROM in the shoulder was limited. I had like really tense muscles in my lower back and pretty much most of my extremities. I remember taking Ibuprofen that night to go to sleep because I had a head ache. The next day I still kind of felt like recovering from a cold like still having the achiness and dizziness like your head is kind of heavy. Its been pretty persistent of those symptoms since then. On 03/23/2021 I had a doctor?s appt and they assured me that we lost our baby and they were worried about my blood pressure, it was 149/106 with pulse of 88. They told me that I should be worried about my blood pressure because that is extremely high and to take caution and monitor it. That is when I started doing the weekly reports. We do not know if the blood pressure was related to the pregnancy but it has come down since then. Since then I still have the occasional head ache and dizziness, right now I am actually sick with cough and mucus and I am schedule to take a Covid test. I had high blood pressure during pregnancy before.


VAERS ID: 1497955 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Indiana  
Vaccinated:2021-03-09
Onset:2021-03-18
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-07-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6199 / 2 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Pregnancy test, Progesterone, Ultrasound abdomen, Uterine dilation and curettage
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: n/a
Preexisting Conditions: n/a
Allergies: NKDA
Diagnostic Lab Data: Labs: Hcg, progesterone Ultrasounds, D&C
CDC Split Type:

Write-up: Pregnancy - I was about 5 weeks pregnant at the time of my second vaccine dose. I started bleeding one week later which resulted in miscarriage. Conceived again in April 2021, which miscarried in June 2021 at 11 weeks requiring D&C. One previous successful pregnancy conceived naturally with no complications.


VAERS ID: 1213705 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-18
Onset:2021-03-18
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ET3620 / 1 LA / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Off label use, Product use issue
SMQs:, Termination of pregnancy and risk of abortion (narrow), Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: FRPFIZER INC2021358212

Write-up: Miscarriage; Maternal exposure during pregnancy, first trimester; Maternal exposure during pregnancy, first trimester; This is a spontaneous report from a contactable consumer reporting for self downloaded from the Regulatory Authority-WEB . A 29-years-old female patient received the first dose of bnt162b2 (COMIRNATY), intramuscular administered in Arm Left on 18Mar2021 (Batch/Lot Number: ET3620) as single dose for covid-19 immunisation. The patient medical history was not reported. The patient''s concomitant medications were not reported. Date of last menstruation was 18Feb2021. The patient experienced spontaneous miscarriage at 4 weeks on 23Mar2021, that is five days after vaccination. The mother reported she became pregnant while taking bnt162b2. The mother was 2 Weeks pregnant at the onset of the event. The mother was due to deliver on 25Nov2021. Patient who did not have COVID-19 and did not perform a test. Patient not knowing her pregnancy status at the time of vaccination. Outcome of event Miscarriage was recovered on23Mar2021. No follow-up attempts possible. No further information expected.


VAERS ID: 1453373 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-03
Onset:2021-03-18
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP9598 / 2 LA / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion, Maternal exposure timing unspecified
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

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:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NOPFIZER INC2021730498

Write-up: maternal exposure during pregnancy; Abortion; This is a spontaneous report from a contactable other Healthcare professional downloaded from the regulatory authority-WEB, regulatory authority number NO-NOMAADVRE-FHI-2021-U38drn. A 45-years-old female patient (patient was pregnant at the time of vaccination) received second dose of BNT162B2 (COMIRNATY, Solution for injection, Lot number: EP9598, Expiration date: unknown) intramuscular, administered in left arm on 03Mar2021 at 09:00 am (age at vaccination was unknown) as 2nd dose, single for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. The patient previously received first dose of BNT162B2 (COMIRNATY, Solution for injection, Lot number: unknown, Expiration date: unknown) via an unspecified route of administration, administered at an unspecified anatomical location on 10Feb2021 (age at vaccination was unknown) as 1st dose, single for COVID-19 immunization. The patient discovered pregnancy on 06Mar2021, three days after she received the second dose of Comirnaty. Nearly two weeks later she had a miscarriage. The source of assessment was reported as regulatory authority. The result of assessment was reported as possible. The outcome of the event was unknown. Sender''s comment: Thank you for reporting a suspected side effect after vaccination. Since the vaccine is new, it is subject to special surveillance to detect new safety information as quickly as possible. It is especially important that serious and / or unusual side effects are reported. Your message is therefore important to increase knowledge about side effects that have not been discovered in the studies, and is an important contribution to international cooperation to maintain safe vaccination worldwide. Reports after corona vaccination in the Adverse Reaction Register are processed by the regulatory authority in collaboration with the regulatory authority. The regulatory authority publishes weekly summaries of reports of suspected side effects after vaccination. Causality is assessed according to international criteria (1). We do not currently have the capacity to send individual adverse reaction reports. For updated information and advice on the use of the vaccines and precautionary rules, please refer to the Vaccination Guide. Advisory service for health professionals The regulatory authority answers general questions about coronary vaccines. Questions can be directed to PRIVACY or by calling the vaccine telephone. We recommend that you contact your GP or other qualified health personnel if you have questions related to your own health. The message should be recorded We recommend that you ask your GP or other doctor to record the message. The following minimum is entered in the patient record: - reference number for the message - which vaccine has been registered - a brief description of symptoms and why it has been reported. No follow-up attempts possible. No further information expected. Lot/Batch number already obtained.; Reporter''s Comments: Reporter type: nurse, ambulance worker No more information available


VAERS ID: 1479711 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-18
Onset:2021-03-18
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / -

Administered by: Other       Purchased by: ?
Symptoms: Maternal exposure during pregnancy, Premature delivery, Premature labour
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: LUSTRAL
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: ILPFIZER INC2021820227

Write-up: Cesarean delivery 07May2021 week 35 + 5 and the baby with a cerebral infarction; Premature labor started 02Apr2021 week 30 + 5 (14 days after vaccination 2); Premature labor started 02Apr2021 week 30 + 5 (14 days after vaccination 2); This is a spontaneous report from two contactable consumers (Patient and her relative). Both consumers reported information for both mother and fetus/baby. This is a maternal report. A 35-years-old pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Batch/Lot number was not reported), via an unspecified route of administration, administered in Arm Left on 18Mar2021 (at the age of 35 years) as dose 2, single for COVID-19 immunization at Public Clinic facility. The patient medical history and Concomitant medication(s) included sertraline hydrochloride (LUSTRAL). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Patient had no known allergies. It was reported that Premature labor started on 02Apr2021, week 30 + 5 (14 days after vaccination 2) Cesarean delivery 07May2021 week 35 + 5 and the baby with a cerebral infarction. The patient gave birth a month and a half after being administered with the second vaccine, contractions began two weeks after the second vaccine. The baby was born with cerebral infarction in the 35th week of pregnancy. The girl was suffering from an infarction. They were not aware of any prior hypercoagulation problems. The patient was about to perform tests to investigate this. The reporter wanted to bring this to our attention due to the proximity to the second vaccination and as he heard of thrombotic events caused by the vaccine in the media. Reporter asked whether it was possible to know if such events were reported in the world, I explained that I am not able to provide this information. The adverse event resulted in Emergency room/department or urgent care, anomaly or Birth defect. It was reported that no therapeutic measures were taken for the events experienced. The mother reported she became pregnant while taking BNT162B2. The mother was 28 Weeks pregnant at the onset of the event. The mother was pregnant with 1 baby(s). The mother was due to deliver on 06Jun2021. The mother delivered the pregnancy on 07May2021 via cesarean delivery. The fetus outcome was abnormal newborn. The outcome of events was unknown.


VAERS ID: 1117742 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Tennessee  
Vaccinated:2021-03-18
Onset:2021-03-19
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-03-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / SC

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Injection site pain
SMQs:, Extravasation events (injections, infusions and implants) (broad), Termination of pregnancy and risk of abortion (narrow)

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: Prentala vitamins
Current Illness: None
Preexisting Conditions: Psoriasis
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pain at injection site starting one day after 2nd pregnancy (first was miscarriage), due date November 12


VAERS ID: 1121867 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: New York  
Vaccinated:2021-02-01
Onset:2021-03-19
   Days after vaccination:46
Submitted: 0000-00-00
Entered: 2021-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / IM

Administered by: Military       Purchased by: ?
Symptoms: Abortion spontaneous, Anembryonic gestation, Laboratory test, Ultrasound antenatal screen
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamins
Current Illness: None
Preexisting Conditions: History of thrombosis
Allergies: None
Diagnostic Lab Data: Ultrasound ER visit Labwork
CDC Split Type:

Write-up: Received COVID vaccine on 1Feb2021 and was currently seeking to become pregnant. I concieved a child on 2Feb2021-4Feb2021. On 19March2021 it was determined that the pregnancy was abnormal and that I had miscarried, with likely diagnosis of blighted ovum.


VAERS ID: 1138434 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2021-03-13
Onset:2021-03-19
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-03-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Blood test taken March 22 and pregnancy test was negative (pregnancy test was positive March 16)
CDC Split Type:

Write-up: Miscarriage at week 5


VAERS ID: 1226011 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-03-14
Onset:2021-03-19
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-04-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Second trimester pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, Vit D
Current Illness: None
Preexisting Conditions: Asthma
Allergies: PCN
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage at 25 weeks. No hx of pregnancy related issues. No hx of miscarriage. Reason for miscarriage not established/no clear reason for miscarriage.


VAERS ID: 1121865 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-03-18
Onset:2021-03-20
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / -

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal, vitamin D, Claritin, stool softener
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Going to Obgyn tomorrow
CDC Split Type:

Write-up: Began spotting 2 days after the vaccine, it progressed over two more days and just had first miscarriage at 2AM on 3/22/2021


VAERS ID: 1139170 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: California  
Vaccinated:2021-03-18
Onset:2021-03-20
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-03-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 003A21A / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Headache, Night sweats, Pain, Pyrexia, Somnolence
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None.
Current Illness: None.
Preexisting Conditions: None.
Allergies: None.
Diagnostic Lab Data:
CDC Split Type:

Write-up: I discovered I was pregnant just after receiving the 2nd dose of the Moderna vaccine. I have had one pregnancy before, six years ago, that ended in a healthy, full-term child with no complications. I received the vaccine on Thursday morning. Thursday evening - Saturday morning I had extreme body aches, fever and night sweats, headache and grogginess. On Saturday evening, my miscarriage began. The estimated date of delivery would have been November 20, 2021.


VAERS ID: 1177150 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-02-05
Onset:2021-03-20
   Days after vaccination:43
Submitted: 0000-00-00
Entered: 2021-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6199 / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Heavy menstrual bleeding, Human chorionic gonadotropin abnormal, Intermenstrual bleeding, Ultrasound scan
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal; vitamin d3
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: sonogram 1: 3/26/2021 sonogram 2: 4/2/2021 blood draws several times a week- 3/10 , 3/15, forgot the third blood draw date, then two more including 4/8
CDC Split Type:

Write-up: I was about 4.5 weeks pregnant with the first dose of the vaccine; and 7.5 weeks with the second dose. After the first dose, my hcg beta hormone level wasn''t rising as fast as it should (ie. it wasn''t doubling to tripling every 2 days) so I had to continue to get blood drawn to monitor it. Then it had one big rise after 1.5 weeks; but soon after, I started spotting lightly daily. After about a week of daily light spotting, I started heavily bleeding (like a menstrual period) on 3/25 (one day before my second dose). I went for a sonogram and it was confirmed that the fetus had no heartbeat. We waited a few days after the second does to redo the sonogram but the bleeding had continued and the second sonogram showed no fetus-- meaning I had a miscarriage where the fetus was naturally eliminated through the bleeding. I am being followed on a weekly basis for blood draws by my obgyn office to ensure that my hcg hormone level falls to 0.


VAERS ID: 1178047 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Oklahoma  
Vaccinated:2021-02-24
Onset:2021-03-20
   Days after vaccination:24
Submitted: 0000-00-00
Entered: 2021-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6202 / 2 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH PAA156051 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Pathology test
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Sertraline 100mg, Prenatal Vitamin, Baby Aspirin, Progesterone Supplement
Current Illness: None
Preexisting Conditions: None
Allergies: Penicillin
Diagnostic Lab Data: Specimen was sent for chromosomal and pathology analysis but results have not been received.
CDC Split Type:

Write-up: Original Due Date: 11/4/2021. Miscarriage discovered 4/5/2021 and suspected to have occurred around 3/20/2021 (baby measured 7weeks,1 day on ultrasound). There were no indications of miscarriage before the ultrasound 4/5/201. Neither me, the patient, nor my doctor believe the miscarriage was a result of the vaccine but as it occurred a few weeks after I received the second dose in the series I felt it should be reported. I was approximately 4 weeks pregnant at the time of my second dose.


VAERS ID: 1240248 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Utah  
Vaccinated:2021-03-09
Onset:2021-03-20
   Days after vaccination:11
Submitted: 0000-00-00
Entered: 2021-04-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6204 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Pregnancy test, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamins, vitamin d
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Obgyn exam on 03/26/2021 by midwife OB/GYN. Pregnancy test to confirm no longer pregnant after all bleeding stopped, self administered on 03/30/2021.
CDC Split Type:

Write-up: Miscarriage at approximately 11 weeks 2 days. 1st pregnancy. Estimated due date Oct 7, 2021.


VAERS ID: 1240260 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Utah  
Vaccinated:2021-03-09
Onset:2021-03-20
   Days after vaccination:11
Submitted: 0000-00-00
Entered: 2021-04-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ENG204 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Haemorrhage, Pregnancy test negative
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins, vitamin d
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: OBGYN exam on 03/26/2021 OB GYN by midwife. Pregnancy test after bleeding stopped on 3/30/2021, self administered to confirm negative pregnancy.
CDC Split Type:

Write-up: Miscarriage at the 11th week of pregnancy. 1st pregnancy; no previous pregnancies, miscarriages or abortions. Estimated due date Oct 7, 2021.


VAERS ID: 1370332 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-03-20
Onset:2021-03-20
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 003B21A / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Headache, Pain in extremity, Product dose omission issue, Vaccination site pain
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad), Medication errors (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:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20211

Write-up: Missed second dose of the Moderna COVID-19 vaccine; Spontaneous abortion; Lot of pain in my whole arm; Exposure during pregnancy; Strong headache; Pain in the muscle where I got the vaccine; This spontaneous case was reported by a consumer and describes the occurrence of ABORTION SPONTANEOUS (Spontaneous abortion) in a 28-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 003B21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 20-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Mar-2021, the patient experienced PAIN IN EXTREMITY (Lot of pain in my whole arm), EXPOSURE DURING PREGNANCY (Exposure during pregnancy), HEADACHE (Strong headache) and VACCINATION SITE PAIN (Pain in the muscle where I got the vaccine). On 08-Apr-2021, the patient experienced ABORTION SPONTANEOUS (Spontaneous abortion) (seriousness criterion medically significant). On an unknown date, the patient experienced PRODUCT DOSE OMISSION ISSUE (Missed second dose of the Moderna COVID-19 vaccine). The patient was treated with IBUPROFEN (oral) at a dose of 500 mg. At the time of the report, ABORTION SPONTANEOUS (Spontaneous abortion), PRODUCT DOSE OMISSION ISSUE (Missed second dose of the Moderna COVID-19 vaccine), PAIN IN EXTREMITY (Lot of pain in my whole arm), EXPOSURE DURING PREGNANCY (Exposure during pregnancy), HEADACHE (Strong headache) and VACCINATION SITE PAIN (Pain in the muscle where I got the vaccine) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were reported. This is a case of product exposure during pregnancy with associated AEs for this 28-year-old female. Very limited information regarding this events has been provided at this time. Further information has been requested. Most recent FOLLOW-UP information incorporated above includes: On 25-May-2021: Followup received contains NNI; Sender''s Comments: This is a case of product exposure during pregnancy with associated AEs for this 28-year-old female. Very limited information regarding this events has been provided at this time. Further information has been requested.


VAERS ID: 1504574 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-20
Onset:2021-03-20
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP9605 / 1 LA / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Inappropriate schedule of product administration, Overdose, Ultrasound scan
SMQs:, Drug abuse and dependence (broad), Termination of pregnancy and risk of abortion (narrow), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnancy normal
Allergies:
Diagnostic Lab Data: Test Name: ultrasound; Result Unstructured Data: Test Result:Both were in very early pregnancy (less than 4 wee; Comments: Both were in very early pregnancy (less than 4 weeks) based on the size of intrauterine gestational sac
CDC Split Type: MYPFIZER INC2021870180

Write-up: I have been having recurrent miscarriages in May 2021 and July 2021. Both were in very early pregnancy (less than 4 weeks) based on the size of intrauterine gestational sac visualised by ultrasound.; patient received dose 1 of Comirnaty and dose 2 of Comirnaty on 20Mar2021 (as per source); patient received dose 1 of Comirnaty and dose 2 of Comirnaty on 20Mar2021 (as per source); This is a spontaneous report from a contactable physician (patient herself). A 34-year-old female patient received BNT162B2 (COMIRNATY, solution for injection), dose 1 via an unspecified route of administration, administered in left arm on 20Mar2021 (Batch/Lot Number: EP9605) as dose 1, single and dose 2 via an unspecified route of administration, administered in left arm on 20Mar2021 (Batch/Lot Number: ER7449) as dose 2, single for COVID-19 immunisation. The patient medical history included 5 successful pregnancies. Concomitant medications were not reported. Patient received dose 1 of Comirnaty and dose 2 of Comirnaty on 20Mar2021 (as per source). Patient reported that she has been having recurrent miscarriages in May2021 and Jul2021. Both were in very early pregnancy (less than 4 weeks) based on the size of intrauterine gestational sac visualised by ultrasound. She had 5 successful pregnancies and no history of miscarriage prior to these two. She has no underlying medical illness. The adverse event resulted in doctor or other healthcare professional office/clinic visit. No treatment was received due to the adverse event. The patient didn''t received any other vaccines within 4 weeks prior to the COVID vaccine and didn''t received other medications within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19 and has not been tested for COVID-19 since the vaccination. The outcome of event was recovering.; Sender''s Comments: Based on the patient''s previous pregnancy history, no history of miscarriage and no underlying medical history the contributory role of the vaccine BNT162B2 to the event early miscarriage cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1134669 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: New York  
Vaccinated:2021-03-17
Onset:2021-03-21
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-03-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 038A21A / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Premature delivery, Stillbirth
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: denied
Preexisting Conditions: denied
Allergies: NKDA
Diagnostic Lab Data: unknown
CDC Split Type:

Write-up: Patient''s OB-GYN called our vaccination center to report that the patient was 30 weeks 3 days pregnant, had an expected due date of 5/27/21 but delivered a stillborn fetus on 3/21/21 at medical center on 3/21/21.


VAERS ID: 1176890 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Hawaii  
Vaccinated:2021-03-12
Onset:2021-03-21
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 036A21A / 2 LA / SYR

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Exposure during pregnancy, Foetal heart rate, Gynaecological examination, Premature labour, Surgery, Ultrasound antenatal screen
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Lithium, Latuda, Concerta
Current Illness:
Preexisting Conditions: Bipolar Disorder
Allergies: Amoxicillian
Diagnostic Lab Data: Ultrasounds, fetal heart monitoring, routine blood work, examination of cervix.
CDC Split Type:

Write-up: Miscarriage of baby at 20 weeks and 3 days of gestation. Preterm labor. Due date was August 6, 2021. Baby was surgically removed on March 22, 2021.


VAERS ID: 1182483 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: New Mexico  
Vaccinated:2021-03-19
Onset:2021-03-21
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-04-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Hashimoto''s thyroiditis
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021321057

Write-up: Miscarriage; This is a spontaneous report from a contactable Other HCP (Nurse), reported for herself. This 39-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number unknown), via an unspecified route in the right arm, on 25Feb2021 at 17:30 (at the age of 39-year-old) as single dose for COVID-19 immunisation and the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number unknown), via an unspecified route in the right arm, on 19Mar2021 at 17:30 (at the age of 39-year-old) as single dose for COVID-19 immunisation. The patient was pregnant at the time of vaccination and the last menstrual date was 02Sep2020. Gestational period 5 weeks and delivery date 19Nov2021. Relevant medical history included Hashimoto''s thyroiditis. Past drug history included allergy to amoxicillin and omeprazole. Relevant concomitant medications included ascorbic acid, betacarotene, calcium sulfate, colecalciferol, cyanocobalamin, ferrous fumarate, folic acid, nicotinamide, pyridoxine hydrochloride, retinol acetate, riboflavin, thiamine mononitrate, tocopheryl acetate, zinc oxide (PRENATAL VITAMINS). No other vaccine was received in four weeks. Pre-vaccination and post-vaccination COVID tests were not performed. On 21Mar2021 (at 14:00), the patient had miscarriage. The event required physician office visit. The patient did not receive any treatment for the event. She was recovering from the event. Information on the lot/batch number has been requested.; Sender''s Comments: Pending the limited information on clinical course, the company does not attribute the event miscarriage to BNT162B2. The detailed document of pregnancy, relevant risk factors, status of Hashimoto''s thyroiditis are missing for a medically meaningful assessment. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1226240 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-03-18
Onset:2021-03-21
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-04-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP7534 / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Foetal heart rate decreased, Haemorrhage, Ultrasound scan
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamins, fish oil
Current Illness: n/a
Preexisting Conditions: n/a; BMI 35
Allergies: light allergy to avocado, broccoli
Diagnostic Lab Data:
CDC Split Type: vsafe

Write-up: 3/18 vaccination 3/21 bleeding 3/22 Ultra sound with low fetal HR. 3/22-/3/23 passing of gestational sac I went back Wed and had another lab work done to compare the levels from Monday to Wed. No other lab work done. 2nd pregnancy, 1 live birth, DOD 11/5/2021


VAERS ID: 1255099 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Maine  
Vaccinated:2021-03-17
Onset:2021-03-21
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-04-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / -

Administered by: Other       Purchased by: ?
Symptoms: Amniotic cavity infection, Chills, Fatigue, Foetal death, Headache, Pain, Premature labour, Pyrexia, SARS-CoV-2 test, Staphylococcal infection
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Atopic dermatitis
Allergies:
Diagnostic Lab Data: Test Date: 20210330; Test Name: covid test type post vaccination= Nasal Swab; Test Result: Negative
CDC Split Type: USPFIZER INC2021390010

Write-up: Chorioamnionitis due to a staph aureus infection; staph aureus infection; fever; preterm labor; My baby did not survive; headaches; fatigue; chills; body aches; This is a spontaneous report from a contactable healthcare professional, the patient. This 38-year-old pregnant female patient reported that she received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: UNKNOWN) via unspecified route in the left deltoid on 17Mar2021 (at the age of 38-years-old) as a single dose for COVID-19 immunization. The patient''s medical history included atopic dermatitis. The patient had allergies to ibuprofen, Aspirin, and Nuvaring. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: EL9261) via an unspecified route in the left arm on 24Feb2021 (at the age of 38-years-old) as a single dose for COVID-19 immunization and experienced headaches, fatigue, chills, and body aches. The patient did not have COVID prior to the vaccination. The patient did not receive any other vaccine in four weeks. Concomitant medication included prenatal vitamin. The patient went into preterm labor on 29Mar2021 which was 12 days after her second dose. She delivered on 30Mar2021 at 21 weeks and 5 days. The patient was diagnosed with chorioamnioitis due to a staph aureus infection. The baby did not survive. Leading up to the hospital admission and after her first and second vaccines, she had frequent headaches and fatigue which she related to the vaccine. She also had chills and body aches. Event start date was reported as 21Mar2021. On admission she had a fever. The events resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care, and hospitalization. The patient was hospitalized for 2 days. She stated that she is reporting this because she is very healthy and developed an unusual uterine infection after the vaccine. She felt that her immune system was affected post vaccine which may have contributed to her ability to fight off infection. The patient did not receive treatment for pre-term labor, baby did not survive, chorioamnioitis, staph aureus infection, frequent headaches, fatigue, chills, body aches, and fever. The clinical outcome of the events pre-term labor, baby did not survive, chorioamnioitis, staph aureus infection, frequent headaches, fatigue, chills, body aches, and fever was unknown. The patient was tested for COVID post vaccination with nasal swab on 30Mar2021, with test result Negative. The lot number for the vaccine, BNT162b2, was not provided and will be requested during follow-up.; Sender''s Comments: Limited information can not support a complete medical assessment. A possible contributory role between BNT162B2 vaccine and the reported events can not be excluded based on current available information and temporal relationship. Case will be re-assessed upon the additional information provided. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.,Linked Report(s) : US-PFIZER INC-2021392327 same report/patient, different dose/AE


VAERS ID: 1382606 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-02-26
Onset:2021-03-21
   Days after vaccination:23
Submitted: 0000-00-00
Entered: 2021-06-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound scan
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: ultrasound 3/21/21
CDC Split Type:

Write-up: embryonic demise at 9 weeks gestation first pregnancy


VAERS ID: 1853546 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Unknown  
Vaccinated:0000-00-00
Onset:2021-03-21
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Arthralgia, Body mass index, Chills, Exposure during pregnancy, Fatigue, Headache, Malaise, Myalgia, Pain in extremity
SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: LAMOTRIGINE
Current Illness: Abstains from alcohol; Multigravida; No previous exposure to drug NOS; Non-tobacco user
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage
Allergies:
Diagnostic Lab Data: Test Name: Body mass index; Result Unstructured Data: 24.26
CDC Split Type: USJNJFOC20210728695

Write-up: SPONTANEOUS ABORTION; MATERNAL EXPOSURE DURING PREGNANCY; CHILLS; FEELING UNWELL; JOINT PAIN; SORE ARM; FATIGUE; HEADACHE; MUSCLE PAIN; This solicited pregnancy report received from a patient concerned a 36 year old white female of an unspecified ethnic origin. The patient was enrolled in a non-company sponsored study. The patient''s weight was 66.67 kilograms, height was 165 centimeters, and body mass index (BMI) was 24.26. The patient''s past medical history included: one previous pregnancy, which resulted in a miscarriage, and concurrent conditions included: multigravida, no history of exposure to drugs for recreational use, tobacco use, or alcoholic beverage consumption. The patient initiated treatment with Covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805029, and expiry: unknown) dose was not reported, 1 total was administered on 21-MAR-2021 for covid-19 immunisation. Concomitant medications included prenatal Vitamin and Lamotrigine. On 21-MAR-2021 (gestational age 3 weeks 6 days), the patient had maternal exposure during pregnancy, chills, feeling unwell, joint pain, sore arm, fatigue, headache, and muscle pain. On 11-May2021 (gestational age 11 weeks and 1 day), the study participant experienced spontaneous abortion. No additional details were provided. The first day of the last menstrual period (LMP) was reported to be 22-Feb-2021. The estimated delivery date (EDD) was calculated to be 29-Nov-2021. It was reported that this was singleton pregnancy. The para was 0 and gravida was 2. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from maternal exposure during pregnancy, chills, feeling unwell, joint pain, sore arm, fatigue, headache, and muscle pain on 23-MAR-2021, and the outcome of spontaneous abortion was not reported. The reporter provided no causality assessment. Company causality between covid-19 vaccine ad26.cov2.s, and spontaneous abortion, and maternal exposure during pregnancy was not related, and between covid-19 vaccine ad26.cov2.s, and chills, feeling unwell, joint pain, sore arm, fatigue, headache, and muscle pain was related. This report was serious (Other Medically Important Condition). Additional information was received from patient on 27-JUL-2021. The following information was updated and incorporated into the case narrative: Race (white), height (165 centimeters), BMI (24.26), medical history (multigravida, no history of exposure to drugs for recreational use, tobacco use, or alcoholic beverage consumption.), concomitant medication (prenatal Vitamin and Lamotrigine), event (spontaneous abortion), seriousness (serious), outcome (unknown), cessation date of previous events, LMP (22-Feb-2021), EDD (29-Nov-2021), para (0), Gravida (2), and narrative was updated accordingly.; Sender''s Comments: V1: 20210728695-Covid-19 vaccine ad26.cov2.s-spontaneous abortion. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: MEDICAL HISTORY 20210728695-Covid-19 vaccine ad26.cov2.s-maternal exposure during pregnancy. This event(s) is considered not related. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS


VAERS ID: 1379434 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-14
Onset:2021-03-21
   Days after vaccination:66
Submitted: 0000-00-00
Entered: 2021-06-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Enuresis, Influenza like illness, Malaise, SARS-CoV-2 test, Scan, Vaccination site pain
SMQs:, Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnancy
Allergies:
Diagnostic Lab Data: Test Date: 20210515; Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test; Test Name: scan; Result Unstructured Data: Test Result:miscarried at approximately 9 weeks
CDC Split Type: GBPFIZER INC2021584670

Write-up: unwell; the arm where vaccine was received; flu like symptoms; bed; Early miscarriage; This is a spontaneous report from a contactable consumer. This is a report received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202105211456213140-FFWXI, Safety Report Unique Identifier GB-MHRA-ADR 25337607. A 37-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 14Jan2021 (Lot number was not reported) at single dose for COVID-19 immunization. The patient was fit and well before vaccination. It is unsure if patient has had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Medical history included pregnancy from an unknown date and unknown if ongoing. Concomitant medications included folic acid taken for folic acid supplementation, start and stop date were not reported. The patient experienced unwell on an unspecified date with outcome of unknown, the arm where vaccine was received on an unspecified date with outcome of unknown , flu like symptoms on an unspecified date with outcome of unknown, bed on an unspecified date with outcome of unknown, early miscarriage on 21Mar2021 with outcome of recovered. The patient was unwell with flu like symptoms for 3 days spent. The patient was in bed, servers pain. The arm where vaccine was received, painkillers taken. Approximately 8-9 weeks later she miscarried second pregnancy. No previous history of miscarriage. Patient was exposed to the medicine first-trimester (1-12 weeks). The patient was no longer pregnant at the time of reporting. Patient has not tested positive for COVID-19 since having the vaccine. The patient underwent lab tests and procedures which included COVID-19 virus test: No - Negative COVID-19 test on 15May2021; scan: miscarried at approximately 9 weeks on an unspecified date. No follow-up attempts are possible; information about lot/batch number cannot be obtained


VAERS ID: 1127239 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-03-09
Onset:2021-03-22
   Days after vaccination:13
Submitted: 0000-00-00
Entered: 2021-03-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ1686 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Ultrasound scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Ultrasound 3/23/2021
CDC Split Type:

Write-up: Miscarriage confirmed on 3/23/2021 at approximately 5 weeks and 6 days.


VAERS ID: 1255216 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-03-18
Onset:2021-03-22
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-04-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6198 / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021392693

Write-up: Late-term miscarriage; This is a spontaneous report from a contactable consumer (patient). A 31-year-old pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EN6198), via an unspecified route of administration on 18Mar2021 as single dose for COVID-19 immunization in a hospital. The patient''s medical history was not reported. There were no concomitant medications. The patient had no other vaccines in four weeks and no other medications in two weeks. The patient has not had COVID prior to vaccination and has not been tested for COVID post vaccination. The patient experienced late-term miscarriage on 22Mar2021 that required physician clinic visit and hospitalization for 1 day. The mother was 15 weeks pregnant at the onset of the event. Gestation period at exposure was not reported. Pregnancy due date was reported to be scheduled on 07Sep2021. The pregnancy resulted in spontaneous abortion. Fetal outcome was not reported. Therapeutic measures were taken as a result of late-term miscarriage which includes dilation and evacuation (D&E). The outcome of the event was unknown.


VAERS ID: 1268135 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-03-12
Onset:2021-03-22
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-04-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6204 / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Caesarean section, Condition aggravated, Exposure during pregnancy, Hypertension, Laboratory test, Premature delivery, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Hypertension (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: High blood pressure medicaiton
Current Illness: High blood pressure
Preexisting Conditions: High blood pressure, chronic
Allergies: NKDA
Diagnostic Lab Data: lab work performed
CDC Split Type: vsafe

Write-up: My BP went extremely high. The reason I went to the hospital initially, because I had some spotting and I was pregnant. I called the doctor and I was advised to go to the ER room. I had no more bleeding, but my BP was way too high. I was a 28 weeks pregnant at the time I went to the ER room. I delivered my baby on 03-29-2021 via emergency C-section.


VAERS ID: 1312872 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Georgia  
Vaccinated:2021-03-22
Onset:2021-03-22
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 023M20A / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: LEXAPRO
Current Illness: Asthma
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20211

Write-up: Patient Miscarried; vaccine exposure during pregnancy; This spontaneous case was reported by a health care professional (subsequently medically confirmed) and describes the occurrence of ABORTION SPONTANEOUS (Patient Miscarried) and EXPOSURE DURING PREGNANCY (vaccine exposure during pregnancy) in a 25-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 023M20A and 030m20a) for COVID-19 vaccination. Concurrent medical conditions included Asthma. Concomitant products included ESCITALOPRAM OXALATE (LEXAPRO) for an unknown indication. On 22-Mar-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Mar-2021, the patient experienced EXPOSURE DURING PREGNANCY (vaccine exposure during pregnancy) (seriousness criterion medically significant). On 30-Apr-2021, the patient experienced ABORTION SPONTANEOUS (Patient Miscarried) (seriousness criterion medically significant). At the time of the report, ABORTION SPONTANEOUS (Patient Miscarried) and EXPOSURE DURING PREGNANCY (vaccine exposure during pregnancy) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment information was reported. Action taken with mRNA-1273 in response to the event was Not Applicable Company Comment: This case concerns a 25-year-old who experienced vaccine exposure during pregnancy and abortion. Abortion occurred 1 month 8 days post mRNA-1273 use. Although a temporal association exist, there is still not enough information to assess the causal association with the product use. Critical details such as the obstetric history including the duration of pregnancy, antenatal history and condition at the time of abortion is lacking. Additional information has been requested.; Sender''s Comments: This case concerns a 25-year-old who experienced vaccine exposure during pregnancy and abortion. Abortion occurred 1 month 8 days post mRNA-1273 use. Although a temporal association exist, there is still not enough information to assess the causal association with the product use. Critical details such as the obstetric history including the duration of pregnancy, antenatal history and condition at the time of abortion is lacking. Additional information has been requested.


VAERS ID: 1334895 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Arizona  
Vaccinated:2021-01-25
Onset:2021-03-22
   Days after vaccination:56
Submitted: 0000-00-00
Entered: 2021-05-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound scan
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Ultrasound
CDC Split Type: vsafe

Write-up: I experienced a Miscarriage 03/22/2021 at five weeks pregnancy. I had gotten the second dose of the vaccine eight weeks before that. I was unaware that I was pregnant when I miscarried. I only found out I was pregnant four days before it happened. Due Date-09/18/2021 Pregnancy-Third


VAERS ID: 1435923 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:2021-03-22
Onset:2021-03-22
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Product dose omission issue
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Medication errors (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20212

Write-up: Pregnancy resulted in a miscarriage; Did not receive 2nd dose; Found out she was pregnant after receiving 1st dose; This spontaneous retrospective pregnancy case was reported by a consumer and describes the occurrence of ABORTION SPONTANEOUS (Pregnancy resulted in a miscarriage) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 22-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 22-Mar-2021, the patient experienced EXPOSURE DURING PREGNANCY (Found out she was pregnant after receiving 1st dose). On an unknown date, the patient experienced ABORTION SPONTANEOUS (Pregnancy resulted in a miscarriage) (seriousness criterion medically significant) and PRODUCT DOSE OMISSION ISSUE (Did not receive 2nd dose). The delivery occurred on an unknown date, which was reported as Abortion NOS. For foetus 1, The outcome was reported as Spontaneous Abortion NOS. On 22-Mar-2021, EXPOSURE DURING PREGNANCY (Found out she was pregnant after receiving 1st dose) had resolved. At the time of the report, ABORTION SPONTANEOUS (Pregnancy resulted in a miscarriage) had resolved and PRODUCT DOSE OMISSION ISSUE (Did not receive 2nd dose) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product use was not provided by the reporter. Treatment information was not provided. It was reported that the patient received first shot and then found out she was pregnant. The pregnancy resulted in a miscarriage and patient wanted to knowif she should now get her 2nd shot, or restart the vaccination series. This is a case of product exposure during pregnancy with an associated adverse event of abortion spontaneous. Based on temporal association a causal relationship cannot be excluded. Also This report refers to a case of Product dose omission. further information is not expected. Reporter did not allow further contact; Sender''s Comments: This is a case of product exposure during pregnancy with an associated adverse event of abortion spontaneous. Based on temporal association a causal relationship cannot be excluded. Also This report refers to a case of Product dose omission. further information is not expected.


VAERS ID: 1526257 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-03-01
Onset:2021-03-22
   Days after vaccination:21
Submitted: 0000-00-00
Entered: 2021-08-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6199 / 1 - / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Ultrasound antenatal screen abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: None
Preexisting Conditions: Seasonal allergies, exercise-induced asthma
Allergies: Soy, tree nuts
Diagnostic Lab Data: Ultrasound 03/22/21
CDC Split Type:

Write-up: Miscarriage of pregnancy


VAERS ID: 1750114 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: California  
Vaccinated:2021-03-08
Onset:2021-03-22
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-09-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 013M20A / 2 RA / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Heavy menstrual bleeding, Intermenstrual bleeding, Maternal exposure before pregnancy, Pregnancy
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: No
Current Illness: None
Preexisting Conditions: ADHD
Allergies: Pencillin
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Patient received vaccine 03/08/2021 which was on her menses. Two weeks later the patient developed heavy bleeding which was unusual for this patient, she has never had mid cycle bleeding. Patient found out she was pregnant the middle of April, and then she had miscarriage at the end of April at home.


VAERS ID: 1275689 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-22
Onset:2021-03-22
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 1063487 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

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: COVID-19 (detected 26Nov2020)
Allergies:
Diagnostic Lab Data:
CDC Split Type: IEPFIZER INC2021409463

Write-up: MISCARRIAGE; This is a spontaneous report from a contactable other hcp downloaded from the Regulatory Authority-WEB, regulatory authority number IE-HPRA-2021-070421. This is a report received from the Ireland''s Health Products Regulatory Authority (HPRA). This is a maternal report. A 32-years-old female patient received bnt162b2 (COMIRNATY), dose 2 via an unspecified route of administration on 22Feb2021 (Batch/Lot Number: 1063487) as 0.3 mL single, and dose 1 via an unspecified route of administration on 25Jan2021 (Batch/Lot number was not reported) as 0.3 mL single both for covid-19 immunisation . Medical history included covid-19 from Nov2020 to an unknown date detected 26Nov2020. The patient''s concomitant medications were not reported. The patient previously took quadrivalent influenza vaccine for prophylaxis. The patient was unaware of pregnancy when 2nd dose was received , she also experienced a miscarriage on 22Mar2021. The mother reported she became pregnant while taking bnt162b2. The mother was 1 Trimester pregnant at the onset of the event. The pregnancy resulted in spontaneous abortion. The fetal outcome is intrauterine death. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1352273 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2020-12-21
Onset:2021-03-22
   Days after vaccination:91
Submitted: 0000-00-00
Entered: 2021-05-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ0553 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, SARS-CoV-2 test
SMQs:, Termination of pregnancy and risk of abortion (narrow), 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: CYCLIZINE; FLUOXETINE; FOLIC ACID; OMEPRAZOLE; ZAPAIN
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Depression; Folic acid supplementation; Indigestion; Nausea; Pain; Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Date: 20210504; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021530029

Write-up: Miscarriage; This is a spontaneous report from a contactable pharmacist received from the Regulatory Agency (RA). The regulatory authority report number is GB-RA-WEBCOVID-202105101800120200-KSBGB. Safety Report Unique Identifier GB-RA-ADR 25274080. This is a maternal report. A 32-year-old female patient (mother) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 21Dec2020 (Batch/Lot Number: V0006/EJ0553) as 1ST DOSE, SINGLE for covid-19 immunisation. Medical history included pregnancy (not ongoing, patient no longer pregnant at the time of reporting), nausea, depression, folic acid supplementation, indigestion and pain. Unsure if patient had had symptoms associated with COVID-19. Unsure if patient was enrolled in clinical trial. Patient was not currently breastfeeding. Concomitant medications included cyclizine taken for nausea from 16Apr2018; fluoxetine taken for depression from 11Jul2018; folic acid taken for folic acid supplementation; omeprazole taken for dyspepsia from 09Nov2016; codeine phosphate, paracetamol (ZAPAIN) taken for pain from 26Nov2018. It was reported that the patient was exposed to the medicine before pregnancy. The patient experienced miscarriage on 22Mar2021. The event was assessed as serious (medically significant). Lab data includes COVID-19 virus test: No - Negative COVID-19 test on 04May2021. The outcome of the event was recovering (as reported). Patient had not tested positive for COVID-19 since having the vaccine. No follow-up attempts are possible. No further information expected.


VAERS ID: 1137248 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Nebraska  
Vaccinated:2021-03-01
Onset:2021-03-23
   Days after vaccination:22
Submitted: 0000-00-00
Entered: 2021-03-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1805020 / 1 LA / IM

Administered by: School       Purchased by: ?
Symptoms: Abortion spontaneous, Cytogenetic abnormality, Exposure during pregnancy, Human chorionic gonadotropin, Stillbirth
SMQs:, Congenital, familial and genetic disorders (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zoloft, 100 mg Prenatal vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: We are still testing the lab results.
CDC Split Type:

Write-up: I had a miscarriage on 3/23/2021 at 6.4 weeks pregnant. I received the vaccine when I was about 4 weeks pregnant. My estimated due date was Nov. 13, 2021. I went to the doctor to get blood drawn to test progesterone and HGC levels. That evening, I miscarried. We are doing testing to see what may have caused the miscarriage but I have not had a miscarriage in the past. On Sept 9, 2020 I experienced a chromosomal stillbirth of a baby boy. His death was due to triploidy which is a fatal chromosomal abnormality.


VAERS ID: 1155161 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-01-19
Onset:2021-03-23
   Days after vaccination:63
Submitted: 0000-00-00
Entered: 2021-04-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1283 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Uterine dilation and curettage
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamin, Colace
Current Illness: n/a
Preexisting Conditions: n/a
Allergies: sulfa
Diagnostic Lab Data: Positive pregnancy tests 2/19, 2/24; pregnancy confirmed via ultrasound 3/23. Estimated gestation age based on last menstrual period (1/20/21) 8 weeks 6 days, fetus measured 6 weeks 2 days. Confirmed loss with drop in Hcg levels on 3/23 and 3/25. D&C performed 3/30/21.
CDC Split Type:

Write-up: miscarriage, d&C on 3/30/21


VAERS ID: 1158268 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-01-23
Onset:2021-03-23
   Days after vaccination:59
Submitted: 0000-00-00
Entered: 2021-04-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure before pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

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: Daily multivitamin
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data:
CDC Split Type:

Write-up: Received second dose of Moderna vaccine on 1/23/21, likely conceived on 1/24/21. Lost pregnancy between 8-9 weeks with noted fetal bradycardia on during ER visit on 3/14/21 and no FHR on 3/18/21.


VAERS ID: 1212100 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-01-28
Onset:2021-03-23
   Days after vaccination:54
Submitted: 0000-00-00
Entered: 2021-04-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 - / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion induced, Exomphalos, Exposure during pregnancy, Multiple congenital abnormalities, Spinal disorder, Ultrasound antenatal screen, Ultrasound foetal abnormal, Ventricular septal defect
SMQs:, Congenital, familial and genetic disorders (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Synthroid Prenatals
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: fetal echo and anatomy scan
CDC Split Type:

Write-up: Moderna Covid 19 vaccine dose 1 -12/29/2020 Positive pregnancy test 1/28/2021 (approximately day 14 gestation) Moderna Covid 19 vaccine dose 2-1/28/2021 12 week nuchal translucency test Maternal fetal medicine doctor diagnosed giant omphalocele (3/23/2021). Follow up visit at 14 weeks (4/6/2021) confirmed giant omphalocele as well as large Ventral septal defect, and spinal abnormalities; diagnosis of Pentalogy of Cantrell; pregnancy terminated


VAERS ID: 1253852 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Alabama  
Vaccinated:2021-03-05
Onset:2021-03-23
   Days after vaccination:18
Submitted: 0000-00-00
Entered: 2021-04-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9264 / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Dizziness, Exposure during pregnancy, Haemorrhage in pregnancy, Post abortion haemorrhage, Uterine spasm, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Anticholinergic syndrome (broad), Vestibular disorders (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Physical exam as well as quant levels checked weekly for 3 weeks.
CDC Split Type:

Write-up: I was exactly 4 weeks pregnant at the time of my second vaccination. On March 23 I started to develop cramping in uterus. On March 25 or March 26 (I cannot remember exactly which day here) I started spotting, and then by the next day I was bleeding. On March 29 I saw my OBGYN who diagnosed me with a miscarriage. I continued to bleed for approximately 10 days, as well as dizziness, and feeling very faint. I have had 2 very healthy pregnancies in the past and no health issues. This could be absolutely unrelated, as early miscarriages are almost impossible to pinpoint, but I did feel this should be reported for researching purposes.


VAERS ID: 1264239 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-02-11
Onset:2021-03-23
   Days after vaccination:40
Submitted: 0000-00-00
Entered: 2021-04-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamins
Current Illness:
Preexisting Conditions:
Allergies: meloxicam, blueberries, keflex
Diagnostic Lab Data:
CDC Split Type:

Write-up: Was pregnant at time of second vaccine should have been approximately 4 weeks but was not aware I was pregnant. At viability ultrasound there was no heart beat and it did not match with how far along i should have been. Repeat ultrasound a week later showed no growth and was diagnosed with a missed miscarriage.


VAERS ID: 1435935 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: California  
Vaccinated:2021-03-23
Onset:2021-03-23
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Headache, Nausea, Vomiting
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20212

Write-up: Miscarriage; she received first moderna vaccine while pregnant; Nausea; Headache; Vomiting; This spontaneous retrospective pregnancy case was reported by a patient and describes the occurrence of ABORTION SPONTANEOUS (Miscarriage) in a 25-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 23-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 23-Mar-2021, the patient experienced EXPOSURE DURING PREGNANCY (she received first moderna vaccine while pregnant), NAUSEA (Nausea), HEADACHE (Headache) and VOMITING (Vomiting). On 15-May-2021, the patient experienced ABORTION SPONTANEOUS (Miscarriage) (seriousness criterion medically significant). The delivery occurred on 15-May-2021. For neonate 1, The outcome was reported as Spontaneous Abortion NOS. On 23-Mar-2021, EXPOSURE DURING PREGNANCY (she received first moderna vaccine while pregnant) had resolved. At the time of the report, ABORTION SPONTANEOUS (Miscarriage), NAUSEA (Nausea), HEADACHE (Headache) and VOMITING (Vomiting) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant product use was not provided. In about a period of two weeks, the ultrasound indicated that the baby''s heart beat was non-existent and on 15 May 2021, the patient had a spontaneous miscarriage. Date of last menstrual period and estimated due date were not provided. No treatment was given. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. This case was linked to MOD-2021-226308 (Parent-Child Link). See case MOD-2021-226308 for details regarding the child case.; Sender''s Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.


VAERS ID: 1457055 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Missouri  
Vaccinated:2021-03-05
Onset:2021-03-23
   Days after vaccination:18
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6204 / UNK - / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Ultrasound antenatal screen abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Pre-natal vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: NA
Diagnostic Lab Data: See item 18 response
CDC Split Type:

Write-up: Ovulated on/around February 22, 2021. Received the first shot on March 5, 2021. Positive pregnancy test on March 12, 2021. March 23, 2021 ultrasound showed fetal sack- no heart beat. This would have been 6 weeks pregnant. April 5, 2021 ultrasound show fetal pole without heart beat- measuring 6 weeks in size (this was 8 weeks pregnant). April 14, 2021 ultra sound showed no heart beat.


VAERS ID: 1187294 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-19
Onset:2021-03-23
   Days after vaccination:63
Submitted: 0000-00-00
Entered: 2021-04-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6134 / 2 RA / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed, Maternal exposure during pregnancy, Ultrasound foetal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: CMV infection
Allergies:
Diagnostic Lab Data: Test Date: 20210227; Test Name: fetal ultrasound; Result Unstructured Data: Test Result:1.5 cm gestational sac; Test Date: 20210302; Test Name: fetal ultrasound; Result Unstructured Data: Test Result:yolk sac, 2 cm gestational sac; Test Date: 20210323; Test Name: fetal ultrasound; Result Unstructured Data: Test Result:2 cm gestational sac, yolk sac -missed abortion
CDC Split Type: HUPFIZER INC2021329993

Write-up: exposure during pregnancy; missed abortion; The initial safety information received was reporting only non-serious adverse drug reaction(s), Upon receipt of follow-up information on (25Mar2021), this case now contains serious adverse reactions. Information processed together. This is a spontaneous report from a contactable physician. This report is received from the Regulatory Authority system with interaction number 00178795. A contactable 30-year-old pregnant female patient reported that she received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EJ6134), via intramuscular route of administration on right upper arm on 19Jan2021 at 09:00 at single dose for COVID-19 immunization. The patient medical history included CMV infection. The patient concomitant medications were not reported. The patient has not received any other vaccine within 4 weeks prior to the vaccine. Historical vaccines included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EJ6796), via intramuscular route of administration on right upper arm on 27Dec2020, 17:00 at single dose for COVID-19 immunization. On 23Mar2021, the patient was diagnosed with pregnant 4 weeks later from her second dose of Pfizer vaccine on the 19th of January and missed abortion (medically significant). The events resulted in Physician Office visit. The laboratory tests included Results of serology tests (e.g., rubella, toxoplasmosis, etc): previous CMV infection, Ante-natal check-ups: Fetal ultrasound(27Feb): 1.5 cm gestational sac; 02Mar2021: yolk sac, 2 cm gestational sac, 23Mar2021: 2 cm gestational sac, yolk sac -missed abortion. There were no previous pregnancies reported. The First day of last menstrual period was reported as 20Jan2021. The estimated date of conception was reported as 26Jan2021.The Estimated delivery date was reported as 27Oct2021. The patient Gestational period at time of initial exposure was 1st month, 1st trimester. The patient has not taken any other drugs (e.g., prescription, over the counter, illicit drugs) during pregnancy. The patient did not smoke or drank alcohol during pregnancy. The outcome of pregnancy was unknown. The treatment received in regard to the event was surgical termination. The outcome of the event was not recovered. Follow-up activities are completed. No further information is expected. Follow-up (25Mar2021): Upon follow up, new information was received from consumer. New information (pregnancy details, laboratory tests, medical history, lot number, event details) were updated.; Sender''s Comments: Based on the limited information currently available, a possible association of the suspect drug administration with the reported event cannot be completely excluded, due to a plausible temporal relationship. This case will be reassessed when additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.


VAERS ID: 1396972 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-23
Onset:2021-03-23
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
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: Miscarriage
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021628630

Write-up: Miscarriage of pregnancy; Found out I was pregnant 2 days after vaccine; This is a spontaneous report. A 34-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 23Mar2021 (Lot number was not reported) as single dose for COVID-19 immunisation. Medical history included Miscarriage. Patient has not had symptoms associated with COVID-19, Not had a COVID-19 test, Patient is not enrolled in clinical trial. The patient''s concomitant medications were not reported. The patient experienced miscarriage of pregnancy on 23Apr2021 with outcome of recovered on 30May2021. Clinical course as reported: Found out I was pregnant 2 days after vaccine and suffered a miscarriage 4 weeks later. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1789240 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-03-23
Submitted: 0000-00-00
Entered: 2021-10-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH NOT KNOWN / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, SARS-CoV-2 test, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Lactation decreased; Pregnancy (Patient no longer pregnant at the time of reporting.); Comments: Patient has not had symptoms associated with COVID-19 Patient is not enrolled in clinical trial Patient is not currently breastfeeding
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021858634

Write-up: Miscarriage; Bleeding vaginal; This is a spontaneous report from two contactable other hcps downloaded from the Regulatory Authority-WEB, regulatory authority number GB-MHRA-WEBCOVID-202107030204297310-XRZ2V, Safety Report Unique Identifier-GB-MHRA-ADR 25589674. A 24-years-old female patient received second dose of bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Batch/Lot number: not known; Expiration Date: not provided), via an unspecified route of administration on an unspecified date as DOSE 2, SINGLE for COVID-19 immunisation. Medical history included pregnancy (patient no longer pregnant at the time of reporting) and lactation decreased from unspecified dates and unknown if ongoing. Patient is not currently breastfeeding. Last menstrual period date: 27Jun2021. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Concomitant medications included folic acid from an unspecified date and unknown if ongoing. On 23Mar2021, the patient experienced bleeding vaginal. On 04Oct2021, it was reported that patient experienced miscarriage on an unspecified date. The event miscarriage was assessed as serious (medically significant), the event bleeding vaginal was assessed as non-serious. The patient underwent lab tests and procedures which included COVID-19 virus test with result of ''negative; No - Negative COVID-19 test'' on an unspecified date. The outcome of the event bleeding vaginal was recovered on 08Jun2021; outcome of the event miscarriage was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. Follow-up (04Oct2021): New information received from two contactable other HCP Via Regulatory Authority-WEB includes additional event and updated patient''s clinical course. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1139749 (history)  
Form: Version 2.0  
Age: 20.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-03-23
Onset:2021-03-24
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-03-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Foetal death
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Fetal demise at 8w3d, one day after receiving first covid vaccine dose.


VAERS ID: 1153376 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-03-19
Onset:2021-03-24
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-03-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6207 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Fatigue, Foetal death, Foetal heart rate abnormal, Pain in extremity, Ultrasound foetal abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: 10mg singulair 10mg Zyrtec 20mg lexapro Prenatal vitamin
Current Illness:
Preexisting Conditions: Asthma
Allergies: Codeine
Diagnostic Lab Data: Ultrasound 3/18/2021 Ultrasound 3/31/2022
CDC Split Type:

Write-up: Pain in arm and fatigue 1-2 days after receiving vaccination. Was 12 weeks 2 days pregnant on vaccination date, estimated due date of 9/27/2021. Fetus confirmed healthy day prior to vaccination via ultrasound on 3/18/2021. Had routine prenatal check on 3/31/2021 and fetal heartbeat could not be found. Fetal demise confirmed via ultrasound the same day, 3/31/2021. Estimated fetus age at demise was 13 weeks 1 day.


VAERS ID: 1155730 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Illinois  
Vaccinated:2021-03-17
Onset:2021-03-24
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-04-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 045A21A / UNK LA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Anembryonic gestation, Arthralgia, Exposure during pregnancy, Pain, Ultrasound foetal abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Arthritis (broad)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Only prenatal vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: Cefzil Sulfa drugs Penicillin
Diagnostic Lab Data: Ultrasound (so far)
CDC Split Type:

Write-up: No real symptoms at time of vaccine. Pain after injection for two days. Pain in right hip for five days. Went in for ultrasound on 4/1/21 at 9 weeks 4 days and found out that there was no fetal pole. Measured at 8 weeks 3 days with gestational sac and yolk sac but no embryo. Considered an embryonic pregnancy, empty sac, or blighted ovum Approximate loss 3/24/21. Still waiting to pass tissue to fully miscarry.


VAERS ID: 1202783 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Nebraska  
Vaccinated:2021-02-02
Onset:2021-03-24
   Days after vaccination:50
Submitted: 0000-00-00
Entered: 2021-04-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: pre natal allergy pill
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: I received both vaccines while pregnant and had a miscarriage at 11 weeks (found out at my 13 week appointment). I had COVID in November 2020.


VAERS ID: 1208930 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Maryland  
Vaccinated:2021-03-17
Onset:2021-03-24
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-04-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Live birth
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal pill, over the counter
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pregnancy history: 2 previous healthy children. Current pregnancy was to be due Nov. 4, 2021, had second shot when 7 weeks pregnant, heard heartbeat at 8 weeks, went to get checked at 11 weeks and it was measured that I miscarried at 8 weeks, exactly one week after receiving the second shot.


VAERS ID: 1293188 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Maryland  
Vaccinated:2021-03-04
Onset:2021-03-24
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-05-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1283 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion induced, Amniocentesis
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Rabbis vaccination 2nd vaccination skin rash
Other Medications: Pre- Natal and baby aspirin
Current Illness: No
Preexisting Conditions: OTC Deficiency as carrier diagnose during permanency and cause of loss.
Allergies: Macrobid
Diagnostic Lab Data: Amino Synthesis
CDC Split Type: vsafe

Write-up: Pregnancy termination at 18 weeks due to un-survivable . OTC Deficiency as carrier diagnose during permanency and cause of loss.


VAERS ID: 1519595 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: West Virginia  
Vaccinated:2021-01-20
Onset:2021-03-24
   Days after vaccination:63
Submitted: 0000-00-00
Entered: 2021-08-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL8982 / 1 LA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9269 / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Foetal heart rate abnormal, Ultrasound antenatal screen abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Ultrasound - 03/24/2021.
CDC Split Type:

Write-up: Miscarriage - ultrasound at 9 weeks showed no fetal heartbeat. Fetus stopped growing at 7 weeks. Estimated delivery date 10/28/2021.


VAERS ID: 1211671 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-22
Onset:2021-03-24
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-04-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Blood test, Dyskinesia, Foetal death, SARS-CoV-2 test, Stillbirth, Ultrasound scan
SMQs:, Neuroleptic malignant syndrome (broad), Dyskinesia (narrow), Noninfectious encephalopathy/delirium (broad), Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Hypertension; Morbid obesity; Obstructive sleep apnoea syndrome
Allergies:
Diagnostic Lab Data: Test Name: Bloods sent; Result Unstructured Data: Test Result:normal; Test Date: 20210325; Test Name: COVID-19 virus test; Test Result: Negative ; Test Name: USS; Result Unstructured Data: Test Result:Normal
CDC Split Type: GBPFIZER INC2021354686

Write-up: intrauterine death; Stillbirth; decreased movements; This is a spontaneous report from a contactable physician received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202103302112375480, Safety Report GB-MHRA-ADR 25053655. A 30-year-old female pregnant patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 22Mar2021 as single dose for COVID-19 immunisation. Medical history included hypertension, Morbid obesity, Obstructive sleep apnoea. Patient had not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. Patient was not currently breastfeeding. Patient has not tested positive for COVID-19 since having the vaccine. Concomitant medication included folic acid taken for vitamin supplementation. The patient attended on 25Mar2021 with decreased movements from 24Mar2021. She was found to have intrauterine death at 38 weeks. No preeclampsia, no abruption, no diabetes. No other cause found for stillbirth. The medicine had an adverse effect on any aspect of the pregnancy. Intrauterine fetal death 48-72 hours after vaccination. Patient was exposed to the medicine Third-trimester (29-40 weeks). Ultrasound scan (USS) was normal. Birth was planned for 39 weeks due to morbid obesity but no other complications of pregnancy had occurred and all was well prior to sudden iufd. (She attended with decreased movements and baby had died). Bloods sent, all normal. Post mortem decision still awaited. The patient had COVID-19 virus test negative on 25Mar2021. The outcome of all events was unknown. All events are considered serious with disability and medically significant. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1459286 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-24
Onset:2021-03-24
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 30001415 / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Injection site swelling, Lymphadenopathy, Myalgia
SMQs:, Rhabdomyolysis/myopathy (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Eosinophilic pneumonia (broad), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
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: No adverse event
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEMODERNATX, INC.MOD20212

Write-up: Zum Zeitpunkt der Impfung bestand eine Fr?hschwangerschaft. Diese endete drei Wochen sp?ter mit einer Fehlgeburt; reminiscent of movements with muscle soreness.; Geschwollene Lymphknoten; Schwellung an der Injektionsstelle; This regulatory authority prospective pregnancy case was reported by a consumer and describes the occurrence of ABORTION SPONTANEOUS (Zum Zeitpunkt der Impfung bestand eine Fr?hschwangerschaft. Diese endete drei Wochen sp?ter mit einer Fehlgeburt) in a 32-year-old female patient who received mRNA-1273 (COVID 19 Vaccine Moderna) (batch no. 30001415) for Prophylactic vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included No adverse event. On 24-Mar-2021, the patient received first dose of mRNA-1273 (COVID 19 Vaccine Moderna) (unknown route) 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 24-Mar-2021, the patient experienced INJECTION SITE SWELLING (Schwellung an der Injektionsstelle). On 25-Mar-2021, the patient experienced LYMPHADENOPATHY (Geschwollene Lymphknoten). On an unknown date, the patient experienced ABORTION SPONTANEOUS (Zum Zeitpunkt der Impfung bestand eine Fr?hschwangerschaft. Diese endete drei Wochen sp?ter mit einer Fehlgeburt) (seriousness criterion medically significant) and MYALGIA (reminiscent of movements with muscle soreness.). The delivery occurred on an unknown date. For neonate 1, The outcome was reported as Spontaneous Abortion NOS. On 26-Mar-2021, INJECTION SITE SWELLING (Schwellung an der Injektionsstelle) had resolved. On 28-Mar-2021, LYMPHADENOPATHY (Geschwollene Lymphknoten) had resolved. At the time of the report, ABORTION SPONTANEOUS (Zum Zeitpunkt der Impfung bestand eine Fr?hschwangerschaft. Diese endete drei Wochen sp?ter mit einer Fehlgeburt) and MYALGIA (reminiscent of movements with muscle soreness.) outcome was unknown. The action taken with mRNA-1273 (COVID 19 Vaccine Moderna) (Unknown) was unknown. The patient reported "After the first vaccination with Moderna, severe swelling of the injection site appeared to be together with pressure/touch pain). The movement of the arm was not restricted but was reminiscent of movements with muscle soreness. Symptoms first appeared on the evening of the vaccination day and persisted for about two days. Moreover, about one to two days after vaccination, there was swelling and pain of the lymph node at the height of the armpits on the vaccinated side of the body. This pain lasted for about two more days and then subsided without consequences or symptoms. No relevant concomitant medications were reported. No treatment information was provided. Most recent FOLLOW-UP information incorporated above includes: On 01-Jul-2021: Translation added on 05-Jul-2021,contains updated inarrative and given event term for muscle soreness.; Sender''s Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.


VAERS ID: 1638268 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-24
Onset:2021-03-24
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-08-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER1749 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Anembryonic gestation, Maternal exposure during pregnancy, SARS-CoV-2 test, Ultrasound scan, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Lactation decreased; Miscarriage; Pregnancy; Suspected COVID-19 (Unsure when symptoms stopped); Vitamin supplementation
Allergies:
Diagnostic Lab Data: Test Date: 20201007; Test Name: COVID-19 virus test; Test Result: Positive ; Comments: Yes - Positive COVID-19 test; Test Name: re-scan; Result Unstructured Data: Test Result:decision was taken to undergo MVA
CDC Split Type: GBPFIZER INC202101040865

Write-up: miscarriage; mild spotting; Blighted ovum; Maternal exposure during pregnancy; This is a spontaneous report from a contactable consumer received from the Regulatory Agency (RA). Regulatory authority report number is GB-MHRA-WEBCOVID-202108120755411100-IWVAB, Safety Report Unique Identifier is GB-MHRA-ADR 25788103. A 33-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: ER1749, Expiry date not reported), via an unspecified route of administration on 24Mar2021 (age at vaccination was 33 years) as DOSE 2, SINGLE for COVID-19 immunization. Medical history included abortion spontaneous, pregnancy, suppressed lactation (lactation decreased), suspected COVID-19 from 06Oct2020 to an unknown date (unsure when symptoms stopped), and vitamin supplementation. Patient was pregnant at the time of vaccination but was no longer pregnant at the time of reporting. Patient was not currently breastfeeding. Concomitant medication included folic acid taken for vitamin supplementation, start and stop date were not reported. Historical vaccine included BNT162B2 on an unspecified date as dose 1, single for COVID-19 immunization. The patient experienced miscarriage on an unspecified date with outcome of unknown, blighted ovum on 19May2021 with outcome of recovered on 27May2021, mild spotting on an unspecified date with outcome of unknown and maternal exposure during pregnancy on 24Mar2021 with outcome of unknown. The patient underwent lab tests and procedures which included sars-cov-2 test: positive on 07Oct2020 Yes - Positive COVID-19 test, and ultrasound scan: decision was taken to undergo MVA on an unspecified date. The event miscarriage was reported as serious, medically significant by the health authority while the other events were non-serious. Case narrative: 2nd dose of the vaccine given around time of conception. Pregnancy resulted in a blighted ovum which was detected at 11 weeks due to some mild spotting. At the re-scan 1 week later - decision was taken to undergo MVA the following day and miscarriage confirmed. Patient had not tested positive for COVID-19 since having the vaccine. Patient was not enrolled in clinical trial. No follow-up attempts are needed. No further information is expected.


VAERS ID: 1145796 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Alaska  
Vaccinated:2021-03-22
Onset:2021-03-25
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-03-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 027A21A / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Human chorionic gonadotropin decreased
SMQs:, Termination of pregnancy and risk of abortion (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins, vitamin D, Estradiol, Endometrin, and Progesterone in Oil
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: 3/22 beta HcG 72 3/25 beta HcG 17 3/29 beta HcG <3
CDC Split Type:

Write-up: I had never been pregnant before and have been undergoing fertility treatments for about two and a half years (6 failed IUIs followed by 2 failed frozen embryo transfers via IVF). I had my third frozen embryo transfer on 3/12, almost exactly the same time Alaska opened vaccine availability to anyone over the age of 16. Our doctor?s advice along with everything we found online showed not much was known about the vaccine, but there was no firm reason to think there would be a problem with getting it in early pregnancy. We also knew that being pregnant would mean higher likelihood of having severe symptoms if I got Covid-19, so I signed up for and was administered the first Moderna vaccine on the day of my first pregnancy test. 3/22 my beta HcG level came back at 72, confirming pregnancy. As is standard, I was asked to come back three days later to confirm appropriate growth in those numbers. By Thursday, March 25th my HcG level had fallen to 17, and by Monday, March 29th that level was less than 3. It?s impossible to know if the vaccine played a role in the early miscarriage, but I wanted to provide the data in case there are any trends or information can be learned from my experience.


VAERS ID: 1186014 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-03-24
Onset:2021-03-25
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-04-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 016B21A / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal heart rate abnormal, Foetal hypokinesia, Low birth weight baby, Stillbirth
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Neonatal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamins
Current Illness: No
Preexisting Conditions: No
Allergies: Penicillin
Diagnostic Lab Data: No labortory
CDC Split Type: vsafe

Write-up: 29 weeks, still born delivery, Estimate date of delivery 06/14/2021 and Birth weight at delivery 2 lbs. 03/24/2021 vaccination then on 03/27/201 was not able to feel the baby movement, had an appointment 04/01/2021 and not heartbeat and delivered. on and Delivered at the hospital. Spoke with the doctor that she got the vaccination.


VAERS ID: 1209601 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-03-19
Onset:2021-03-25
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-04-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: multivitamins
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: miscarriage a week after receiving Janssen vaccine


VAERS ID: 1220313 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-03-16
Onset:2021-03-25
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-04-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1805018 / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Exposure during pregnancy, Haemorrhage in pregnancy, Human chorionic gonadotropin, Ultrasound antenatal screen abnormal, Uterine dilation and curettage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: prenatal vitamins, 15mg adderall 3 times a day, pristiq 50mg 1 time a day
Current Illness: None
Preexisting Conditions: None
Allergies: Amoxicillin, hydromorphone, seafood, shrimp, pollin
Diagnostic Lab Data: 3/17/2021 - Ultrasound showing nonviable pregnancy. 3/18/2021 - Blood Draw to check HCG level. 3/20/2021 - Blood Draw to check HCG Level. 3/23/2021 - Ultrasound confirming nonviable pregnancy. 4/2/2021 - labs for checking blood chemistry and pathology test on miscarriage products
CDC Split Type:

Write-up: Spontaneous Abortion. Miscarriage started on it''s own at home. Bleeding lasted 14 days, then turned to excessive hemorrhaging and ended up getting an emergency D&C. Was 10 weeks pregnant at time of miscarriage. EDD was 10/23/2021.


VAERS ID: 1242256 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Oklahoma  
Vaccinated:2021-03-04
Onset:2021-03-25
   Days after vaccination:21
Submitted: 0000-00-00
Entered: 2021-04-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 014M20A / 2 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Pregnancy, Pruritus
SMQs:, Anaphylactic reaction (broad), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Dexilant Pepsid Zoloft Hydrocortisone 2.5% ointment Prenatal vitamin Allegra Vitamins
Current Illness:
Preexisting Conditions: Gastroparesis GERD Idiopathic Peripheral Neuropathy Lichen Planus
Allergies: Penicillin Seasonal Allergies
Diagnostic Lab Data: Blood Work
CDC Split Type: vsafe

Write-up: I found out that I was pregnant four weeks after the second dose. I started to itch all over my body four weeks after the shot. I did not have a visible rash, but my dermatologist said it was a histamine reaction. I was intensely itchy for three days and then it went away after five days. I had a miscarriage five weeks after the second dose which was a week after the itch started. I saw my OBGYN, PCP ER , Gastroenterologist and Dermatologist. Due Date: 12/11/2021 Pregnancy Third Pregnancy


VAERS ID: 1283392 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: Missouri  
Vaccinated:2021-03-06
Onset:2021-03-25
   Days after vaccination:19
Submitted: 0000-00-00
Entered: 2021-05-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 036A21A / 1 RA / -

Administered by: Other       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal death, Foetal growth restriction, Foetal heart rate abnormal, Uterine dilation and curettage
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: None
Preexisting Conditions: Endometriosis
Allergies: Allergic to penicillin
Diagnostic Lab Data:
CDC Split Type:

Write-up: Vaccine received in first trimester of IVF pregnancy with a female, genetically tested normal embryo. Fetus discovered to have no heartbeat, with growth estimated to have ceased 2.5 weeks after vaccine. Fetus measured 11w6d at time of death. D&C performed on 4/2/2021 and fetus tested for abnormalities, with all results returned as normal.


VAERS ID: 1299199 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Florida  
Vaccinated:2021-03-08
Onset:2021-03-25
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-05-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6204 / 1 RA / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion threatened, Blood glucose abnormal, Dizziness, Foetal death, Ultrasound scan, Vertigo
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Anticholinergic syndrome (broad), Vestibular disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: METFORMIN; GLIPIZIDE; LEXAPRO; MECLIZINE [MECLOZINE HYDROCHLORIDE]
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Fatty liver; Fruit allergy; High cholesterol; Type 2 diabetes mellitus
Allergies:
Diagnostic Lab Data: Test Name: ultrasound; Result Unstructured Data: Test Result:heartbeat at 132 bpm; Test Date: 20210423; Test Name: ultrasound; Result Unstructured Data: Test Result:absence of heartbeat; Comments: absence of heartbeat and estimated the embryo stopped growing at 7 weeks
CDC Split Type: USPFIZER INC2021456113

Write-up: absence of heartbeat and estimated the embryo stopped growing at 7 weeks; had a very difficult time keeping her glucose levels; lightheaded; possible threatened miscarriage; persistent vertigo; This is a spontaneous report from a contactable consumer (patient). A 37-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Right on 08Mar2021 at 11:00 (Lot Number: EN6204) as single dose for covid-19 immunisation, administered at the hospital. No other vaccine received in four weeks. Medical history included type 2 diabetes, fatty liver disease, high cholesterol, and known allergies: Pineapples and Zoloft. Concomitant medications included metformin; glipizide; escitalopram oxalate (LEXAPRO); and meclozine hydrochloride (MECLIZINE [MECLOZINE HYDROCHLORIDE]). The patient was pregnant at the time of vaccination. The patient''s last menstrual period was on 03Feb2021. On 25Mar2021, 03:00 PM, patient sought treatment for persistent vertigo at a hospital and was given meclizine. On 03Apr2021, patient went to the emergency room to be assessed for a possible threatened miscarriage. They found her embryo sac and determined she was pregnant. She was released and told to go home. Patient is a type 2 diabetic and was ordered to go on insulin. On 05Apr2021, she had another threatened miscarriage and returned to the hospital. She was given an ultrasound and her due date changed from 10Nov2021 to 28Nov2021. Ultrasound discovered a heartbeat at 132 bpm. On 23Apr2021, at a routine ultrasound and OB visit, doctor discovered absence of heartbeat and estimated the embryo stopped growing at 7 weeks. She was electing for a D&C surgical procedure and requesting pathology testing to investigate the cause of death. She had a very difficult time keeping her glucose levels within the recommended pregnancy range of 90-150. She had persistent lightheaded still. Outcome of events vertigo, possible threatened miscarriage, and lightheaded was not recovered. The patient received treatment for vertigo and did not receive treatment for other events.


VAERS ID: 1351169 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-01-27
Onset:2021-03-25
   Days after vaccination:57
Submitted: 0000-00-00
Entered: 2021-05-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 037K20A / 2 RA / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion induced, Biopsy chorionic villous abnormal, Exposure during pregnancy, Fluorescent in situ hybridisation, Foetal disorder, Ultrasound scan abnormal
SMQs:, Malignancy related therapeutic and diagnostic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Sertraline 100mg, vitamin D, prenatal vitamin
Current Illness:
Preexisting Conditions: Anxiety, depression
Allergies: Nitrofurantoin (Macrobid), Percocet, Benzoyl Peroxide
Diagnostic Lab Data: Ultrasound 3/25/2021 Chorionic villus sampling with FISH and microarray 3/30/2021 Ultrasound 4/22/2021
CDC Split Type:

Write-up: Received dose 2 on 1/27/2021, when I was 4w0d pregnant. Estimated date of delivery 10/06/2021. Ultrasound at 12w1d revealed increased fetal nuchal translucency of 4.56mm. Further testing revealed a de novo 16p11.2 chromosomal duplication. Ultrasound at 16w1d revealed cystic hygroma measuring 8mm with nuchal cyst/septation, and unilateral right club foot. The pregnancy was terminated for medical reasons on 4/30/2021 at 17w1d.


VAERS ID: 1456683 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-04-16
Onset:2021-03-25
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0153 / 2 LA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: SERTRALINE; LORATADINE
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021775397

Write-up: Miscarriage/IUFD at approximately 17 weeks pregnant.; . The mother was 10 weeks pregnant at the onset of the event; This is a spontaneous report received from a contactable consumer (patient). This is a maternal report. A 31-year-old pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, lot number: EW0153 at the age of 31-year-old), dose 2 via an unspecified route of administration, administered in arm left on 16Apr2021 12:30 as single, dose 1 via an unspecified route of administration, administered in arm left on 25Mar2021 12:30 (batch/lot number: EP6955) as single for COVID-19 immunisation. The patient''s medical history was not reported. Concomitant medications included sertraline, loratadine taken for an unspecified indication and prenantal. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not tested for COVID-19. The patient experienced miscarriage/IUFD at approximately 17 weeks pregnant on any unknown date Jun2021. The mother reported she became pregnant while taking BNT162B2. The mother was 10 weeks pregnant at the onset of the event. The mother was due to deliver on 07Nov2021. The patient received treatment was dilation and evacuation for the event. The event resulted in doctor or other healthcare professional office/clinic visit. The fetal outcome was intrauterine death. The outcome of the event miscarriage/IUFD at approximately 17 weeks pregnant was resolving. The outcome for the other event was unknown. Follow-up attempts are completed. No further information was expected.


VAERS ID: 1486991 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-02-26
Onset:2021-03-25
   Days after vaccination:27
Submitted: 0000-00-00
Entered: 2021-07-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 002A21A / 1 LA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 021B21A / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Anembryonic gestation, Maternal exposure during pregnancy, Pathology test, Ultrasound abdomen abnormal, Uterine dilation and curettage
SMQs:, Retroperitoneal fibrosis (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: ultrasound pathology of pregnancy tissues
CDC Split Type:

Write-up: blighted ovum seen on ultrasound followed by miscarriage. post 5 weeks of 1st injection. eventual follow up ultrasounds and D&C.


VAERS ID: 1498477 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-02-21
Onset:2021-03-25
   Days after vaccination:32
Submitted: 0000-00-00
Entered: 2021-07-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 031M20A / 2 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Asymptomatic COVID-19, Exposure during pregnancy, Hypertension, Pre-eclampsia, Premature delivery, SARS-CoV-2 antibody test positive, SARS-CoV-2 test positive
SMQs:, Neuroleptic malignant syndrome (broad), Hypertension (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal Supplement, Baby Aspirin
Current Illness: None.
Preexisting Conditions: Polycystic Ovarian Syndrome
Allergies: None.
Diagnostic Lab Data: March 25th, 2021, Covid Rapid Test - positive, Covid swab - positive; March 26, 2021, Covid antibody test - have Covid antibodies
CDC Split Type: vsafe

Write-up: Well in mid March I was diagnosed randomly with pre-eclampsia. Then later on I was admitted to the hospital after having high BP and I was put on magnesium and labetalol. I delivered my daughter on March 28, 2021. I also tested positive for Covid-19 and then an antibody test as well. I was unable to see my daughter in the NICU due to being positive for the COVID, but luckily my daughter tested negative. So I have never been pregnant before, and my daughter was supposed to be due on May 6th 2021. My daughter''s birth weight was 3lbs and 3 ounces. I was discharged from the hospital on March 30th 2021. I was sent home with BP medication as well and that I was on for about four weeks, and it is nifedipine (60MG 1x daily for two weeks and then 30MG 1x daily for two weeks). I have also seen my OBGYN two weeks post giving birth and another appointment 6 weeks post birth as well. Also, just to say, I had no COVID symptoms when I tested positive for COVID. Like I said, my daughter tested negative but also, my mother was in the hospital room with me and all that, and my mother tested negative as well.


VAERS ID: 1805953 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-03-22
Onset:2021-03-25
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 00B21A / 1 UN / SYR
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 041B2!A / 2 UN / SYR

Administered by: Work       Purchased by: ?
Symptoms: Abortion missed, Exposure during pregnancy, Ultrasound antenatal screen abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Pre-Natal pill and Fish Oil
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Ultrasound occurring on April 8, 2021 showed that i had had a missed miscarriage, the baby had died but did not miscarry naturally.
CDC Split Type:

Write-up: I was pregnant with my fourth pregnancy (three healthy pregnancies and births previous to this fourth pregnancy, no history of miscarriage) and was due October 28, 2021. I had not yet had my first appointment with my doctor as that occurred the first week in April. I had my first vaccination on March 22 and it is estimated that the baby died around March 25 due to its size. When I went for my first appointment on April 8 there was no heartbeat. While it is unlikely the vaccine caused this adverse reaction, I wanted to have it documented in the rare even there were other similar complications.


VAERS ID: 1234741 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-04
Onset:2021-03-25
   Days after vaccination:49
Submitted: 0000-00-00
Entered: 2021-04-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN1185 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Endocrine test, SARS-CoV-2 test, Scan
SMQs:, Termination of pregnancy and risk of abortion (narrow), 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: Mood change; Pregnancy (All previous pregnancies of patient had been healthy)
Allergies:
Diagnostic Lab Data: Test Date: 2021; Test Name: Blood test given for hormone levels; Result Unstructured Data: Test Result:unknown results; Test Date: 20210228; Test Name: COVID-19 virus test; Test Result: Negative ; Test Date: 2021; Test Name: scans; Result Unstructured Data: Test Result:Miscarriage
CDC Split Type: GBPFIZER INC2021375597

Write-up: Early miscarriage; This is a spontaneous report from a contactable consumer (patient) received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202104051737490070. A 37-year-old female patient received first dose of BNT162B2 via an unspecified route of administration on 04Feb2021 (Lot Number: EN1185, expiration date was unknown) as single dose for covid-19 immunisation. Medical history included mood altered. All previous pregnancies of patient had been healthy. The patient underwent lab tests included COVID-19 virus test was negative on 28Feb2021. There were no known allergies or known underlying health issues. Patient did not have symptoms associated with COVID-19. She was not enrolled in clinical trial and was not currently breastfeeding. The patient''s concomitant medications were not reported. Patient was exposed to BNT162B2 Before pregnancy. She became pregnant while taking bnt162b2, conceived around same time as vaccine. And she had early miscarriage on 25Mar2021. Patient discovered she was pregnant 23Mar2021 around 6/7 weeks. 2 days later (25Mar2021) she started bleeding bits here and there and left for another day visited hospital who said threatened miscarriage. She believed she fully miscarried on 31Mar2021. She had a scan with miscarriage. Blood test was given for hormone levels. Patient no longer pregnant at the time of reporting. Patient has not tested positive for COVID-19 since having the vaccine. All other pregnancies were healthy. The outcome of event was recovering. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1145902 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: Utah  
Vaccinated:2021-03-16
Onset:2021-03-26
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-03-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1805018 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Ultrasound pelvis
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: unknown
Preexisting Conditions: periodontal disease
Allergies: nkda
Diagnostic Lab Data: pelvic ultrasound showing yolk sac and gestational sac but no fetal pole after previously seen on ultrasound, bHCG 5000$g 741
CDC Split Type:

Write-up: spontaneous abortion at approximately 8 weeks gestation, 10 days after vaccine administration


VAERS ID: 1242154 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-02-23
Onset:2021-03-26
   Days after vaccination:31
Submitted: 0000-00-00
Entered: 2021-04-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: NONE
Current Illness: none
Preexisting Conditions: none
Allergies: NONE
Diagnostic Lab Data: D&C due to my miscarriage
CDC Split Type:

Write-up: I received my second dose of the Pfizer vaccine on February 23rd 2021. That same day I discovered I was pregnant. On March 26th 2021 at my 9 week appointment ultrasound I discovered that my baby had no heartbeat.


VAERS ID: 1371319 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-03-26
Onset:2021-03-26
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8730 / 2 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Ruptured ectopic pregnancy, Salpingectomy, Surgery, Ultrasound pelvis abnormal
SMQs:, Malignancy related therapeutic and diagnostic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Uterine and fallopian tube malignant tumours (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: Congenital Diaphragmatic Hernia
Allergies: None
Diagnostic Lab Data: Ultrasound and emergency surgery
CDC Split Type: vsafe

Write-up: I had an ectopic pregnancy that wasn''t diagnosed and eventually ruptured, which resulted in the loss of the pregnancy. I had to have emergency surgery and my left fallopian tube had to be removed.


VAERS ID: 1415700 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-03-26
Onset:2021-03-26
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood thyroid stimulating hormone decreased, Exposure during pregnancy, Hypothyroidism, Thyroid disorder
SMQs:, Hypothyroidism (narrow), Hyperthyroidism (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Immune-mediated/autoimmune disorders (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: Lithium, Seroquel, Lorazepam, prenatal vitamin and vitamin D
Current Illness: None
Preexisting Conditions: Hypertension
Allergies: None
Diagnostic Lab Data: 3/26 suppressed tsh
CDC Split Type:

Write-up: Thyroid low TSH hyperthyroidism and miscarriage in two weeks


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