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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: 1042126 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-02-10
Onset:2021-02-16
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-02-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

Administered by: Public       Purchased by: ?
Symptoms: 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? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: Azythromycin
Diagnostic Lab Data:
CDC Split Type:

Write-up: Unknowingly pregnant at time of vaccination. Had a miscarriage one week later. Due on October 12.


VAERS ID: 1059615 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Tennessee  
Vaccinated:2021-01-15
Onset:2021-02-16
   Days after vaccination:32
Submitted: 0000-00-00
Entered: 2021-02-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / IM

Administered by: Unknown       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? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: NKA
Diagnostic Lab Data: Confirmed miscarriage at OB appt 2/24/2021
CDC Split Type:

Write-up: Miscarriage after receiving first Moderna vaccine dose


VAERS ID: 1124657 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-02-09
Onset:2021-02-16
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Cytogenetic analysis, Exposure during pregnancy, Foetal death, Immunology test, Uterine dilation and evacuation
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? Yes
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: prenatal vitamin
Current Illness:
Preexisting Conditions: none
Allergies: Minocycline, clomid
Diagnostic Lab Data: Autoimmune workup, genetic workup, D and E performed 3/8/2022
CDC Split Type:

Write-up: Received 2nd dose of covid vaccine at 11 weeks, 6 days. Had follow up normal ultrasound at 12 weeks, 2 days. Missed miscarriage noted at 15 weeks, 1 day. Last measurement of baby noted to be 12 weeks, 6 days. Closely monitored during first trimester with no abnormalities noted. Normal ultrasound at 12 weeks, several days after baby stopped growing with fetal demise at some point there after


VAERS ID: 1140276 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2020-12-28
Onset:2021-02-16
   Days after vaccination:50
Submitted: 0000-00-00
Entered: 2021-03-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 026L20A / 1 AR / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 004M20A / 2 AR / IM

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal death, Hydrops foetalis, Immunology test, Rhesus antibodies positive
SMQs:, Haemolytic 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? 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: aspirin, cetirizine, famotidine, prenatal vitamin
Current Illness: Rh alloimmunization
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: 38 year old G2P1001 at 22 weeks and 4 days presents with hydrops fetalis. Known anti-D antibodies. Titer initially <1 at 11 weeks. Rapid rise seen with increased anti-D antibody to 1:16 on 1/15/21, and 1:512 on 2/21/2021. Fetus treated with umbilical cord transfusion at 22 weeks 5 days. Fetal death diagnosed at 23 weeks and 0 days. Fetal autopsy consistent with hemolysis in fetal organs. Fetal blood type RHD positive. Immunofixation studies show no monoclonal protein detected.


VAERS ID: 1176336 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Rhode Island  
Vaccinated:2021-01-21
Onset:2021-02-16
   Days after vaccination:26
Submitted: 0000-00-00
Entered: 2021-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 026L20A / 1 LA / IM

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: Unknown
Current Illness: Unknown
Preexisting Conditions: Unknown
Allergies: Unknown
Diagnostic Lab Data: NA- this was given as part of employee health- patient followed up with her own OB for care
CDC Split Type:

Write-up: Reporting as employee health: Staff member reported that she had miscarried as of 2/16/21


VAERS ID: 1350861 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-02-03
Onset:2021-02-16
   Days after vaccination:13
Submitted: 0000-00-00
Entered: 2021-05-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029L20A / 1 AR / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029A21A / 2 AR / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Foetal death, Foetal disorder, Placenta praevia, Placenta praevia haemorrhage, Subchorionic haemorrhage, Ultrasound scan abnormal
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), 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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: celexa, baby aspirin, HCTZ, progesterone vaginal suppositories, levothyroxine
Current Illness:
Preexisting Conditions: low thyroid, post partum high blood pressure, depression
Allergies: compazine
Diagnostic Lab Data: 2/16/2021 - ultrasound at ORM to confirm miscarriage 5/20/2021 - Providence Portland hospital ultrasound to see if surviving baby is still alive and to diagnose placenta previa, 5/24/2021 - anatomy scan ultrasound at Northwest Perinatal
CDC Split Type:

Write-up: 1/20/2021 - got two 5 day old blastocysts implanted via IVF 2/3/2021 - first dose Moderna 2/16/2021 - lost female twin, had sub chorionic hemorrhage. (Both twins were repeatedly tested and had normal chromosomes) 3/3/2021 - second dose Moderna 5/20/2021 - diagnosed complete Placenta previa after bleeding 5/24/2021 - had anatomy scan, surviving male twin has only kidney (renal agenesis)


VAERS ID: 1749351 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: New York  
Vaccinated:2021-02-08
Onset:2021-02-16
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-09-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 039KZOA / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal death, Ultrasound antenatal screen 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? 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: Synthroid 175, Prenatal Vitamin, Vitamin D 2000 iu, Baby Aspirin 1.5/day
Current Illness: None
Preexisting Conditions: Hypothyroid
Allergies: None
Diagnostic Lab Data: On February 16, 2021 an ultrasound was performed which diagnosed the fetal demise. A second ultrasound was preformed by another doctor (also on 2/16/2021) to confirm the fetal demise. A d&c procedure was performed on 2/23/2021.
CDC Split Type:

Write-up: I was 14 weeks pregnant when I received the first dose of the moderna vaccine, on Feb 8, 2021. On February 16 I went for a routine checkup to my OBGYN and the baby was found without a heartbeat. The baby was measured to be 13 weeks 5 days or 13 weeks 6 days, however these are just estimates and are not necessarily exact. I have a history of carrying smaller babies, so it is possible that the baby''s gestational age was greater than 13 weeks 5 or 6 days. My original estimated date of delivery was August 9, 2021.


VAERS ID: 1064914 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-09
Onset:2021-02-16
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK4244 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Pregnancy 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? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID; PREGNACARE ORIGINAL [ASCORBIC ACID;BETACAROTENE;BIOTIN;CALCIUM PANTOTHENATE;COLECALCIFEROL;COPPER;CY
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Allergies:
Diagnostic Lab Data: Test Name: PREGNANCY TEST; Test Result: Positive
CDC Split Type: GBPFIZER INC2021177834

Write-up: Miscarriage; This is a spontaneous report from a contactable healthcare professional. This is a report received from the RA. Regulatory authority report number GB-MHRA-WEBCOVID-202102161957489340, Safety Report Unique Identifier GB-MHRA-ADR 24776283. A 30-years-old female patient (pregnant) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), Lot number EK4244, via an unspecified route of administration on 09Feb2021 at single dose for covid-19 immunisation. Medical history was none. Concomitant medication included folic acid for Vitamin supplementation, ascorbic acid, betacarotene, biotin, calcium pantothenate, colecalciferol, copper, cyanocobalamin, folic acid, iodine, iron, magnesium, nicotinamide, phytomenadione, pyridoxine hydrochloride, riboflavin, selenium, thiamine mononitrate, tocopheryl acid succinate, zinc (PREGNACARE ORIGINAL) from 01Sep2020. Patient had not had symptoms associated with COVID-19. Not had a COVID-19 test. Patient had not tested positive for COVID-19 since having the vaccine. The patient did not know she was pregnant when receiving the vaccine. She tested positive for pregnancy 36 hours after the vaccine. She had Miscarriage on the 16Feb2021 - one week following the vaccine. The outcome of the event was not resolved. No follow-up attempts are possible. No further information expected.


VAERS ID: 1100128 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-28
Onset:2021-02-16
   Days after vaccination:19
Submitted: 0000-00-00
Entered: 2021-03-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM0477 / 1 LA / OT

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Ultrasound scan, Vaccination site pain
SMQs:, Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (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: Medical History/Concurrent Conditions: Pregnancy (previous; normal)
Allergies:
Diagnostic Lab Data: Test Name: ultrasound; Result Unstructured Data: Test Result:uncertainty as to whether it was an ectopic; Comments: uncertainty as to whether it was an ectopic pregnancy or not
CDC Split Type: NOPFIZER INC2021212856

Write-up: vaccination site pain/tenderness; abdominal pain; SPONTANEOUS ABORTION; This is a spontaneous report from a contactable physician. This is a spontaneous report downloaded from the Regulatory Authority-WEB, regulatory authority number (NO-NOMAADVRE-FHI-2021-U9jxz) and Sender''s (Case) Safety Report Unique Identifier (NO-NOMAADVRE-E2B_00016035). A 34-year-old female pregnant patient received first dose of BNT162B2 (tozinameran) (COMIRNATY, solution for injection) lot number EM0477 and expiry date unknown, intramuscular at left arm on 28Jan2021 17:00 at single dose for Covid-19 immunization. The patient''s medical history included previous pregnancies and had been normal. Concomitant medications were not reported. On unspecified date after vaccination with dose one, the patient experienced vaccination site pain/tenderness and no systemic reactions (no fever). On 16Feb2021, the patient experienced spontaneous abortion. The physician informed that the patient was 3 weeks pregnant at the time of the first dose with Covid-19 vaccine (Comirnaty), without knowing she was pregnant. The patient found out that she was pregnant one week after the vaccination. She then had a spontaneous abortion in week 6 of pregnancy. The patient had abdominal pain from week 4 (unspecified date) of the pregnancy. An ultrasound was therefore performed (unspecified date) due to possible ectopic pregnancy and the result was uncertainty as to whether it was an ectopic pregnancy or not. The outcome of the events was unknown. The event spontaneous abortion was considered serious as other medically important condition. The reporter informed that source of assessment: the result of assessment was possible. Regulatory Authority''s comments: 22Jan2021 RELIS: additional information received from reporter by phone. The following fields have been updated: Event description. Sender''s comments: A 34 years old woman was 3 weeks pregnant at the time of the first dose with covid-19 vaccine (Comirnaty), without knowing she was pregnant. She found out she was pregnant one week after the vaccination. She then had a spontanous abortion in week 6 of pregnancy. Additional information: -She had abdominal pain from week 4 of the pregnancy. An ultrasound was therefore performed due to possible ectopic pregnancy. Result: uncertainty as to whether it was an ectopic pregnancy or not. - Reactions after vaccination with dose 1: Vaccination site pain/tenderness. No systemic reactions (no fever). - Her previous pregnancies have been normal. ADDITIONAL INFORMATION ON DRUG PROVIDED IN PRODUCT NOTES Sender Comment: A 34 years old woman was 3 weeks pregnant at the time of the first dose with covid-19 vaccine (Comirnaty), without knowing she was pregnant. She found out she was pregnant one week after the vaccination. She then had a spontanous abortion in week 6 of pregnancy. Spontaneous abortion can have many causes, and often the cause is not known in each case. When vaccinating patients, some serious events may occur shortly after vaccination without any connection to vaccination. However, it cannot be ruled out that the vaccine may have caused the incident. In the case in question, it is difficult to know whether the miscarriage is due to the vaccine or something else accidental, at the same time a cause that has nothing to do with the vaccination in question. On the basis of the information in the report and in accordance with international criteria, the causal relationship with vaccination is assessed as possible. A possible causal relationship is defined as a reaction, including pathological laboratory tests, which occurs in a temporal relation to the use of a drug, but which may also be due to an underlying disease, other drugs or chemicals. No follow-up attempts are possible. No further information is expected.; Reporter''s Comments: 22/jan/2021 RELIS: additional information received from reporter by phone. The following fields have been updated: Event description.; Sender''s Comments: By close temporal relationship the company cannot completely exclude there is a reasonable possibility that the reported serious event of Spontaneous abortion is related to the suspect drug Comirnaty. The impacts 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: 1100181 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-22
Onset:2021-02-16
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-03-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6134 / UNK - / 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? 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: SEPFIZER INC2021208171

Write-up: Miscarriage of pregnancy; This is a spontaneous report downloaded from the Regulatory Authority-WEB [Regulatory Authority number SE-MPA-2021-005718] from a contactable physician. Other case identifier number SE-MPA-1613731711921. A 26-year-old female patient received bnt162b2 (COMIRNATY) (lot# EJ6134), intramuscular, on 22Jan2021, at 0.3 mL single, for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient was pregnant and was pregnant at the time of vaccination. The patient experienced miscarriage of pregnancy (medically significant) on 16Feb2021. The mother was 5 weeks pregnant at the onset of the event, last menstrual period 08Jan2021. The mother was due to deliver on 15Oct2021. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1371609 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Maine  
Vaccinated:2021-02-10
Onset:2021-02-17
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-06-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 016M20A / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Laboratory test, Malaise, 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? No
Hospitalized? No
Previous Vaccinations:
Other Medications: No medications taken at the time of vaccination.
Current Illness: No illnesses at the time of vaccination.
Preexisting Conditions: No chronic health conditions.
Allergies: No known allergies.
Diagnostic Lab Data: I had an ultrasound and labs done.
CDC Split Type: vsafe

Write-up: After the second dose, I was sick the whole next day and I miscarried the following week.


VAERS ID: 1158623 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-01
Onset:2021-02-17
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-04-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 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? 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: NLPFIZER INC2021297552

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer downloaded from the Regulatory Authority-WEB. The regulatory authority report number is NL-LRB-00461368. A 30-year-old female patient received her second dose of BNT162B2 (COMIRNATY), via an unspecified route of administration on 01Feb2021 (Batch/Lot Number: Unknown) as a single dose for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. The first day of the last menstrual period was 13Jan2021. On 10Feb2021, she was overdue and had a positive test. The patient experienced miscarriage (other medically important condition) on 17Feb2021 following administration of COVID-19 Pfizer vaccine. The miscarriage occurred at approximately gestational age 5 weeks. Outcome of event was recovered on 24Feb2021. Sender Comment: Since the nature of the reported reaction does imply seriousness according to one of the CIOMS critera, the reaction was considered as serious by the Regulatory Authority. No follow-up attempts are possible. Information on Batch/lot cannot be obtained.


VAERS ID: 1275301 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-17
Onset:2021-02-17
   Days after vaccination:31
Submitted: 0000-00-00
Entered: 2021-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK1768 / 1 - / -

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

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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: pregnancy test; Test Result: Positive ; Comments: Had her first vaccine before positive pregnancy test; Test Date: 20200801; Test Name: COVID-19 virus test; Test Result: Positive ; Comments: Yes - Positive COVID-19 test
CDC Split Type: GBPFIZER INC2021422544

Write-up: Early miscarriage; This is a spontaneous report from a contactable consumer. This is a report received from the Regulatory Agency. The regulatory authority report number is, GB-MHRA-WEBCOVID-202104151311062050. Safety Report Unique Identifier GB-MHRA-ADR 25144721. A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: ek1768), via an unspecified route of administration on 17Jan2021 as single dose for COVID-19 immunisation. Patient had not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. The patient medical history and concomitant medications were not reported. The patient experienced early miscarriage (abortion spontaneous) on 17Feb2021. Seriousness criteria reported as medically significant, congenital anomaly and hospitalized. Had her first vaccine before positive pregnancy test, 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: positive on 01Aug2020 (Yes-Positive COVID-19 test). Outcome was not recovered. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1400991 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-17
Onset:2021-02-17
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Exposure during pregnancy, 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? 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: ESOPRAM; OMEPRAZOLE; TELFAST
Current Illness: Allergy NOS; Anxiety; Reflux gastritis
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: ISMODERNATX, INC.MOD20212

Write-up: Stillborn; vaccine exposure during pregnancy; This regulatory authority case was reported by a physician and describes the occurrence of STILLBIRTH (Stillborn) in a 26-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. Concurrent medical conditions included Anxiety, Allergy NOS and Reflux gastritis. Concomitant products included FEXOFENADINE HYDROCHLORIDE (TELFAST) for Allergy NOS, ESCITALOPRAM OXALATE (ESOPRAM) for Anxiety, OMEPRAZOLE for Reflux gastritis. On 17-Feb-2021, the patient received first dose of mRNA-1273 (Moderna CoviD-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2021, the patient experienced EXPOSURE DURING PREGNANCY (vaccine exposure during pregnancy). On 11-Mar-2021, the patient experienced STILLBIRTH (Stillborn) (seriousness criteria medically significant and congenital anomaly). At the time of the report, STILLBIRTH (Stillborn) and EXPOSURE DURING PREGNANCY (vaccine exposure during pregnancy) outcome was unknown. The action taken with mRNA-1273 (Moderna CoviD-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna CoviD-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No treatment details reported. This is a case of Exposure during pregnancy with associated Stillbirth. Very limited information regarding Stillbirth has been provided at this time. No further information is expected. Company causality for Stillbirth is assessed as possible, while company causality for Exposure during pregnancy is not applicable.; Sender''s Comments: This is a case of Exposure during pregnancy with associated Stillbirth. Very limited information regarding Stillbirth has been provided at this time. No further information is expected. Company causality for Stillbirth is assessed as possible, while company causality for Exposure during pregnancy is not applicable.


VAERS ID: 1495893 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-17
Onset:2021-02-17
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6790 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Haemorrhage in pregnancy, Inappropriate schedule of product administration, Maternal exposure before pregnancy, Menstrual disorder, Ultrasound 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? 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: Folic acid supplementation; Pregnancy (one previous successful pregnancy)
Allergies:
Diagnostic Lab Data: Test Date: 20210320; Test Name: blood tests; Result Unstructured Data: Test Result:miscarriaged; Comments: confirmed early miscarriage/ miscarriage; Test Date: 20210320; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:miscarriaged; Comments: confirmed early miscarriage/ miscarriage
CDC Split Type: GBPFIZER INC2021859699

Write-up: Bleeding/ she became pregnant...after 5 weeks, patient had some bleeding; erratic periods; Early miscarriage/ miscarriage; patient received the first dose of BNT162B2 on 11Dec2020 and the second dose on 17Feb2021; Maternal exposure during pregnancy/ patient was exposed to the medicine before pregnancy; This is a spontaneous report from a contactable consumer received from the Regulatory Agency (RA); the Regulatory Authority report number is GB-MHRA-WEBCOVID-202107051031312490-8QAEH and the Safety Report Unique Identifier is GB-MHRA-ADR 25594910. A 37-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 17Feb2021 (batch/lot number: EJ6790) at 37 years old as DOSE 2, SINGLE for COVID-19 immunization. The patient''s medical history included one previous successful pregnancy (dates not reported) and folic acid supplementation from an unknown date. The patient was not enrolled in clinical trial. Patient was not currently breastfeeding. Patient has not had symptoms associated with COVID-19 and has not had a COVID-19 test. Concomitant medication included folic acid (FOLIC ACID) taken for folic acid supplementation, start and stop date were not reported. The patient previously received BNT162B2 via an unspecified route of administration on 11Dec2020 (batch/lot number: EJ0553) as DOSE 1, SINGLE for COVID-19 immunization and experienced exposure to the medicine before pregnancy. The patient received the first dose of BNT162B2 on 11Dec2020 and the second dose on 17Feb2021. The patient experienced maternal exposure during pregnancy reported as patient was exposed to the medicine before pregnancy on 17Feb2021. It was reported that the patient had her second dose of the COVID-19 vaccine in 17Feb2021. The following month (Mar2021), she became pregnant. The patient was exposed to the medicine before pregnancy. It was further reported that after 5 weeks (date not reported), patient had some bleeding. An ultrasound scan and blood tests, one week later (on 20Mar2021) confirmed she has had an early miscarriage/ miscarriage. She then had very erratic periods for two months following this. It was unsure if the vaccine had an adverse effect on any aspect of the pregnancy. The patient recovered from the event "early miscarriage/ miscarriage" on 01May2021 (as reported). Outcome of the events "Maternal exposure during pregnancy/ patient was exposed to the medicine before pregnancy," "Bleeding/ she became pregnant...after 5 weeks, patient had some bleeding," and "erratic periods" were unknown. The events were reported as medically significant. The patient has not tested positive for COVID-19 since having the vaccine. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1668090 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-14
Onset:2021-02-17
   Days after vaccination:34
Submitted: 0000-00-00
Entered: 2021-09-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ELO141 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Infertility tests, Pregnancy test, 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: Pregnancy (Patient no longer pregnant at the time of reporting.)
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid supplementation; Lactation decreased
Allergies:
Diagnostic Lab Data: Test Name: scans or investigations; Result Unstructured Data: Test Result:Heavy fresh bleeding per vaginum; Comments: heavy fresh bleeding per vaginum at 6 weeks gestation; Test Name: pregnancy test; Result Unstructured Data: Test Result:Positive; Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021276011

Write-up: Spontaneous abortion; Bleeding vaginal; This is a spontaneous report from other healthcare professional. This is a report received from the Regulatory Agency (RA). The regulatory authority report number is, GB-MHRA-WEBCOVID-202103121300072290. Safety Report Unique Identifier GB-MHRA-ADR 24926676. A 25-year-old female patient received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: ELO141, Expiry date: unknown), via an unspecified route of administration on 14Jan2021 at the age of 25 years old as single dose for COVID-19 immunization. Medical history included suppressed lactation, ongoing pregnancy (patient no longer pregnant at the time of reporting) and folic acid supplementation. Concomitant medication included folic acid at 400 ug taken for folic acid supplementation. Patient has not had symptoms associated with COVID-19. Unsure if patient is enrolled in clinical trial. Patient is not currently breastfeeding. Had vaccine prior to being aware of pregnancy and having a positive pregnancy test. Last menstrual period was on 26Dec2020. Patient has not tested positive for COVID-19 since having the vaccine. Patient was exposed to the medicine first-trimester (1-12 weeks). The patient experienced maternal exposure during pregnancy on 14Jan2021 and bleeding vaginal on 17Feb2021. On 30Jun2021, it was reported that patient had a spontaneous abortion on an unknown date. The events were reported as non-serious by the regulatory authority. The patient underwent lab tests and procedures which included infertility tests: heavy fresh bleeding per vaginum at 6 weeks gestation, sars-cov-2 test negative on an unspecified date and pregnancy test positive all on an unspecified date. Outcome of bleeding vaginal was recovered on 22Feb2021 while outcome for other event was unknown. No follow-up attempts are possible. No further information is expected. Follow-up (30Jun2021): This is a spontaneous report from other healthcare professional. This is a report received from the Regulatory Agency (RA). The regulatory authority report number is, GB-MHRA-WEBCOVID-202103121300072290, Safety Report Unique Identifier is GB-MHRA-ADR 24926676. New information includes: new event (spontaneous abortion). No follow-up attempts are possible. No further information is expected.


VAERS ID: 1668660 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-17
Onset:2021-02-17
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-09-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Exposure during pregnancy, 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? 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: ESOPRAM; OMEPRAZOLE; TELFAST
Current Illness: Anxiety; Reflux gastritis
Preexisting Conditions: Medical History/Concurrent Conditions: Allergy NOS
Allergies:
Diagnostic Lab Data:
CDC Split Type: ISMODERNATX, INC.MOD20212

Write-up: Andvana f??ing; Vaccine exposure during pregnancy; This case was initially received via regulatory authority (Reference number: IS-IMA-2006) on 08-Jun-2021. The most recent information was received on 25-Aug-2021 and was forwarded to Moderna on 25-Aug-2021. This regulatory authority retrospective pregnancy case was reported by a physician and describes the occurrence of STILLBIRTH (Andvana f??ing) in a 26-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. Concurrent medical conditions included Anxiety, Allergy NOS and Reflux gastritis. Concomitant products included FEXOFENADINE HYDROCHLORIDE (TELFAST) for Allergy NOS, ESCITALOPRAM OXALATE (ESOPRAM) for Anxiety, OMEPRAZOLE for Reflux gastritis. On 17-Feb-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 17-Feb-2021, the patient experienced EXPOSURE DURING PREGNANCY (Vaccine exposure during pregnancy). On 11-Mar-2021, after starting mRNA-1273 (Moderna CoviD-19 Vaccine), the patient experienced STILLBIRTH (Andvana f??ing) (seriousness criteria medically significant and congenital anomaly). The delivery occurred on an unknown date, which was reported as Still birth. For foetus 1, The outcome was reported as Stillbirth w Congenital Anomaly. On 17-Feb-2021, EXPOSURE DURING PREGNANCY (Vaccine exposure during pregnancy) had resolved. At the time of the report, STILLBIRTH (Andvana f??ing) outcome was unknown. The action taken with mRNA-1273 (Moderna CoviD-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna CoviD-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No treatment details reported. Based on the outcome of the autopsy the vaccination is not considered to be a causal factor in stillbirth. No Treatment medications were reported. Company Comment: This is a case of Exposure during pregnancy with associated Stillbirth. Very limited information regarding Stillbirth has been provided at this time. No further information is expected. Based on reporter''s causality the vaccination is not considered to be a causal factor in stillbirth, hence it is assessed as unlikely related to mRNA-1273, while company causality for Exposure during pregnancy is not applicable. Most recent FOLLOW-UP information incorporated above includes: On 25-Aug-2021: Significant follow up case: Translation document received on 25 Aug 2021 include information regarding the autopsy and causal relationship between drug and event. On 25-Aug-2021: Translation document received on 25 Aug 2021 include no new information.; Sender''s Comments: This is a case of Exposure during pregnancy with associated Stillbirth. Very limited information regarding Stillbirth has been provided at this time. No further information is expected. Based on reporter''s causality the vaccination is not considered to be a causal factor in stillbirth, hence it is assessed as unlikely related to mRNA-1273, while company causality for Exposure during pregnancy is not applicable.


VAERS ID: 1044756 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: New York  
Vaccinated:2021-01-22
Onset:2021-02-18
   Days after vaccination:27
Submitted: 0000-00-00
Entered: 2021-02-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0142 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3247 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Foetal heart rate abnormal, 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)

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: synthroid prenatal vitamin calcium supplement
Current Illness: none
Preexisting Conditions: hypothyroid
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: I received my first dose of the COVID19 Pfizer vaccine on 12/30/20. At this point I was 4 weeks pregnant. I received my second vaccine dose for the series on 1/22/21. At this point I was 7 weeks pregnant. On 2/18/21 I was diagnosed with a miscarriage due to no fetal heartbeat on ultrasound. I now have to undergo a D&C in the operating room.


VAERS ID: 1063601 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Arizona  
Vaccinated:2021-01-16
Onset:2021-02-18
   Days after vaccination:33
Submitted: 0000-00-00
Entered: 2021-03-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Haemorrhage, Muscle spasms, Pregnancy, Pregnancy test positive
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Dystonia (broad), 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
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: US of pregnancy (Feb 14th), then confirming pregnancy loss (Feb 18th)
CDC Split Type:

Write-up: COVID vaccine given Dec 24th, 2020 and second dose on Jan 16th, 2021. Conception occurred approx Jan 11th, 2021 pregnancy diagnosed Jan 26th, 2021. ED Oct 4th, 2021. US confirmation of pregnancy with gestational sac on Feb 14th, 2021. Miscarriage/SAB/pregnancy loss occurred spontaneously on Feb 18th, 2021 with bleeding, cramping. Pregnancy loss confirmed by ultrasound with OBGYN.


VAERS ID: 1066027 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-02-17
Onset:2021-02-18
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 010M20A / 1 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Blood test, Exposure during pregnancy, Laboratory test, Premature delivery, Premature labour, Urine analysis
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? 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, iron supplement
Current Illness: None
Preexisting Conditions: None
Allergies: Sensitivity to penicillin
Diagnostic Lab Data: Admitted to Hospital late on 2/18/2021, was discharged on 2/21/2021. There were lots of tests and labs done due to the labor (e.g. urine analysis, bloodwork).
CDC Split Type:

Write-up: I was 34 weeks, 5 days pregnant at the time of vaccination (due date 3/26/2021). The next day at 10pm my water broke and I went into early labor. I had my baby on Friday in the early morning. Prior to this, I had no risks or warning signs of early labor (e.g. preeclampsia, gestational diabetes, etc) and was generally following a routine pregnancy path.


VAERS ID: 1069747 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-01-06
Onset:2021-02-18
   Days after vaccination:43
Submitted: 0000-00-00
Entered: 2021-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9261 / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Foetal heart rate abnormal, Laboratory test, Muscle spasms, Ultrasound scan
SMQs:, Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Dystonia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Ultrasound 2/26 Blood work and ultrasound 2/27 Ultrasound 2/21
CDC Split Type:

Write-up: Became pregnant end of December. Received first dose January 6 and second dose January 27. Had very bad side effects. Felt pregnancy symptoms up until February 10th. Symptoms started to linger off. Had ultrasound that showed fetus February 10. Cramping started feeling days later. Had ultrasound again February 18 showed fetus had grown. Had another ultrasound February 21 after going to ED for bad cramping and pain. fetus had no heart beat. Miscarried February 26. Contents did not pass completely, had D&C February 27.


VAERS ID: 1086484 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-02-13
Onset:2021-02-18
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-03-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Human chorionic gonadotropin negative, 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? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: When I started bleeding, my doctor did blood draws weekly. On 2/25/21, when I miscarried I was sent in for more blood draw. It went down from 14,000 to 603. My last blood draw was 3/8/21 and I went from 603 to 41. I have an appointment tomorrow with my primary care doc.
CDC Split Type:

Write-up: I got the Covid vaccine on 2/13/21, I lost a small clot and started to bleed on 2/19/21. I was due around Oct 4th, at the time of the vaccine I was 6 weeks pregnant. I miscarried at home on 2/25/21- I lost a very large clot and was bleeding heavily for a week. Doctor confirmed with HCG test that I miscarried. This was my second pregnancy, I had my first child 1/10/20.


VAERS ID: 1090818 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-01-25
Onset:2021-02-18
   Days after vaccination:24
Submitted: 0000-00-00
Entered: 2021-03-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029L20A / 2 LA / IM

Administered by: Private       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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: My last period was Jan 7, 2021. Received Vaccine, dose 2 on 1/25/21 (I did not know I was pregnant at that time). Had a miscarriage and lost baby Feb 18-21


VAERS ID: 1097090 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-02-18
Onset:2021-02-18
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-03-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9266 / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test normal, Computerised tomogram normal, Electrocardiogram abnormal, Palpitations
SMQs:, Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), 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: zoloft
Current Illness:
Preexisting Conditions: Depression Anxiety Ehlers syndrome
Allergies: Demerol
Diagnostic Lab Data: EKG- abnormal (urgent care) EKG- abnormal (ER) Blood work- Normal (ER) long heart CT Scan- normal (ER)
CDC Split Type: vsafe

Write-up: A couple of minutes of having the vaccine I started having heart palpitations. I didn''t see much of it so I left but it kept on going for the next couple of days then on the following Sunday I ended up going to the urgent care & they sent me to the Emergency room from there. On march 1st I had a miscarriage I was 6 weeks pregnant, There was some questions when I found out I was pregnant to see if I was going to have some issues or not.


VAERS ID: 1106398 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-09
Onset:2021-02-18
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-03-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion missed, Chlamydia test negative, Exposure during pregnancy, Full blood count, Glycosylated haemoglobin, Treponema test negative, Urine analysis, 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? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data: CBC unremarkable on 2/4/2021 and 2/18/2021. UA unremarkable 2/4/2021. Chlamydia/GC PCR negative, quantiferon TB negative, syphilis negative 2/4/2021. Varicella and Rubella titers positive for immunity 2/4/2021. HgbA1c 5.0 2/4/2021.
CDC Split Type:

Write-up: Initial prenatal visit on 2/4/2021, pregnancy measuring 6 weeks with visible cardiac activity. Vaccine received 2/9/2021. Repeat ultrasound 2/18/2021, no cardiac activity seen, pregnancy still measuring 6 weeks. D&C procedure on 2/23/2021 for missed abortion.


VAERS ID: 1111960 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Georgia  
Vaccinated:2021-02-04
Onset:2021-02-18
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-03-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Ultrasound scan vagina
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 medicatiom
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Transvaginal US
CDC Split Type:

Write-up: Miscarriage G3P2 2002


VAERS ID: 1116359 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-01-25
Onset:2021-02-18
   Days after vaccination:24
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 026L20A / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound antenatal screen
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: Ultrasound
CDC Split Type: vsafe

Write-up: After my second vaccine, and few weeks later, I suffered a miscarriage on 02-18-2021. I went to see my OBGYN who performed an ultrasound. My baby at that time was 6 weeks old.


VAERS ID: 1536472 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: New York  
Vaccinated:2021-02-03
Onset:2021-02-18
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-08-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 028L20A / 2 AR / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Human chorionic gonadotropin, Ultrasound uterus abnormal, 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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamins, vitamin D
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Ultrasounds, quantitative HCG blood tests
CDC Split Type:

Write-up: I had a miscarriage beginning on 2/18/21. The EDD of this pregnancy was 9/3/2021. I had another miscarriage on 6/1/21 . The EDD of this pregnancy was 1/10/22. Both miscarriages were incomplete and required D&Cs.


VAERS ID: 1151019 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-09
Onset:2021-02-18
   Days after vaccination:40
Submitted: 0000-00-00
Entered: 2021-03-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM0477 / 1 - / -

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:
Allergies:
Diagnostic Lab Data:
CDC Split Type: IEPFIZER INC2021287606

Write-up: Miscarriage; This is a spontaneous report from a contactable Pharmacist downloaded from the Regulatoty Authority. Regulatory authority report number IE-HPRA-2021-068458, with Safety Report Unique Identifier IE-HPRA-2021-068458. A 33-year-old female patient received first dose of BNT162B2 (COMIRNATY), via an unspecified route of administration on 09Jan2021 (Lot Number: EM0477) as single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient experienced vaccine exposure during pregnancy on 09Jan2021, and miscarriage on 18Feb2021. It was reported that on 09Jan2021, the patient was vaccinated with her first dose. On 18Feb2021, the patient experienced a missed miscarriage, at 8 weeks and 5 days gestation. The patient outlined that she was not aware she was pregnant when she received the first dose, as it was too early to tell. The patient outlined that her obstetrician advised her that miscarriage was unlikely due to the vaccine, given the background risk in the population. The patient was 1 Trimester pregnant at the onset of the event. Outcome of miscarriage was recovered in 2021. On 26Feb2021, the patient was vaccinated with her second dose of BNT162B2. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1158716 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-13
Onset:2021-02-18
   Days after vaccination:36
Submitted: 0000-00-00
Entered: 2021-04-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK1768 / 1 - / -

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

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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: CABERGOLINE; FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Asthma; Folic acid supplementation; Macroprolactinaemia; Pregnancy (uneventful pregnancy)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test; Test Date: 20210216; Test Name: ultrasound scan; Result Unstructured Data: Test Result:missed miscarriage; Comments: should have been 12+3 showed that the fetus had no heartbeat and had stopped growing at 8-9 weeks gestation, approx 1-2 weeks after administration of the first vaccine dose
CDC Split Type: GBPFIZER INC2021300836

Write-up: Early miscarriage/miscarriage; This is a spontaneous report from a contactable consumer received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202103162223205360, Safety Report Unique Identifier GB-MHRA-ADR 24960761. A 32-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EK1768), via an unspecified route of administration on 13Jan2021 at a single dose for COVID-19 immunization. Medical history included asthma, macroprolactinaemia and folic acid supplementation, all from an unknown date and unknown if ongoing and pregnancy (uneventful pregnancy) from 2019. The patient had one previous uneventful pregnancy with spontaneous vaginal delivery in 2019. Patient has not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. Patient was not currently breastfeeding. Concomitant medications included cabergoline taken for macroprolactinaemia from 15Jan2005 to 05Dec2020; and folic acid taken for folic acid supplementation, start and stop date were not reported. The patient experienced early miscarriage/miscarriage on 18Feb2021. The mother was 12 weeks pregnant at the onset of the event. The mother was due to deliver on 28Aug2021. Last menstrual period (LMP) date was 21Nov2021 giving an estimated due date (EDD) of 28Aug2021. First vaccine dose was received on 13Jan2021 at 7+4 weeks gestation. Routine ultrasound scan on 16Feb2021 at what should have been 12+3 showed that the fetus had no heartbeat and had stopped growing at 8-9 weeks gestation, approximately 1-2 weeks after administration of the first vaccine dose. Natural miscarriage then began on 18Feb2021 and continued for approximately 5 days. It was unsure if the medicine has an adverse effect on any aspect of the pregnancy. The reporter assessed the event as serious (hospitalization, medically significant and congenital anomaly). 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: negative (no/negative COVID-19 test) on an unspecified date, and ultrasound scan: missed miscarriage (should have been 12+3 showed that the fetus had no heartbeat and had stopped growing at 8-9 weeks gestation, approximately 1-2 weeks after administration of the first vaccine dose) on 16Feb2021. The outcome of the event was recovered with sequel on an unspecified date. No follow up attempts are possible. No further information is expected.


VAERS ID: 1109817 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-13
Onset:2021-02-19
   Days after vaccination:37
Submitted: 0000-00-00
Entered: 2021-03-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1491 / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed, Ultrasound scan
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: Test Date: 20210111; Test Name: Echography; Result Unstructured Data: Test Result:Gestational age by ultrasound: 5 + 0.; Comments: A gestational sac was observed with an increased yolk vesicle and embryonic echoes.; Test Date: 20210219; Test Name: Echography; Result Unstructured Data: Test Result:missed abortion; Comments: Uterus is seen in retro with gestation week in which the embryonic echoes seen in previous ultrasound are no longer observed, only remnants of distorted vulva and vagina. The diagnosis of missed abortion is confirmed.
CDC Split Type: ESPFIZER INC2021226086

Write-up: Abortion missed; This is a spontaneous report received from a contactable physician downloaded from the Regulatory Authority-WEB. The regulatory authority report number is ES-AEMPS-766995. This is the first of two reports. This 39 year old female patient received BNT162B2 (COMIRNATY, lot number: EL1491, single dose via intramuscular route of administration on 13Jan2021 for COVID-19 vaccination. There was no relevant medical history reported. Concomitant medications were not reported. On 08Feb2021 the patient came in for a consultation after a pregnancy test +. G1. She did not remember the date of the last period. It was not clear if she had her period in Dec2020 or not, so an echo to date the pregnancy was requested. On 19Feb2021, the patient experienced a missed abortion. Laboratory data included echography ulatrasound: a gestational sac was observed with an increased yolk vesicle and embryonic echoes on 11Jan2021 and 19Feb2021 missed abortion: uterus is seen in retro with gestation week in which the embryonic echoes seen in previous ultrasound are no longer observed, only remnants of distorted vulva and vagina. The diagnosis of missed abortion is confirmed. Came in for an ultrasound control for suspected AD vs incipient pregnancy. Uterus is seen in retro with gestation week in which the embryonic echoes seen in previous ultrasound are no longer observed, only remnants of distorted vulva and vagina. The diagnosis of missed abortion was confirmed. Therapeutic options are offered and medical treatment is decided. 800 mcg of intravaginal misoprostol is administered. Appointment in a week for control. No follow-up attempts possible. No further information expected.; Sender''s Comments: Linked Report(s) : ES-PFIZER INC-2021273284 Same patient, different drug and event


VAERS ID: 1113942 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-02-20
Onset:2021-02-20
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6201 / UNK - / -

Administered by: Unknown       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? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: STELARA
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021238565

Write-up: miscarriage; pregnant patient received BNT162B2; pregnant patient received BNT162B2; This is a spontaneous report from a non-contactable consumer. This consumer (patient) that a 34-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: en6201) at the age of 34-years, via an unspecified route of administration on 20Feb2021 at single dose for COVID-19 immunisation. Medical history was not reported. Patient was pregnant at time of vaccination, last menstrual date was 21Jan2021. No other vaccine in four weeks, no COVID-19 prior vaccination. Concomitant medication included ustekinumab (STELARA). The patient experienced miscarriage on an unspecified date (on 03Feb2021, as reported). The pregnant patient received BNT162B2 on 20Feb2021. No COVID-19 tested post vaccination. Outcome of the event was unknown. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : US-PFIZER INC-2021238716 Same product and AE , different patient


VAERS ID: 1175386 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-02-19
Onset:2021-02-20
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9267 / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Fatigue, Full blood count, Pain in extremity, Ultrasound antenatal screen, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Nexium, Prenatal
Current Illness: no
Preexisting Conditions: no
Allergies: strawberries, gluten
Diagnostic Lab Data: CBC Pregnancy Hormone Level 3 Ultrasounds
CDC Split Type: vsafe

Write-up: The next morning after I had arm pain and was very fatigued which lasted about a week. On 2/27 I started experiencing on and off vaginal bleeding but drs had no treatment they could provide. I was diagnosed with a threathened miscarrage and on 3/22/2021 I miscarried. EDD-11/7/2021. There were several bouts of bloodwork perfomed which were normal until the miscarrage occurred and all ultrasounds were normal until the 3rd which showed the miscarriage.


VAERS ID: 1272057 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-20
Onset:2021-02-20
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, 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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage at 7 weeks in pregnancy. No other history of miscarriage and very sudden. Decidual cast.


VAERS ID: 1119484 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-05
Onset:2021-02-20
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-03-21
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, 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? 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: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test; Test Name: scan; Result Unstructured Data: Test Result:Unknown result
CDC Split Type: GBPFIZER INC2021246583

Write-up: 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-202103050843182300, Safety Report Unique Identifier GB-MHRA-ADR 24879937. A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection)(lot number: not reported, expiration date not reported), via an unspecified route of administration on 05Feb2021 at single dose for covid-19 immunisation. Medical history included Miscarriage. Unsure if patient had had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. The patient''s concomitant medications were not reported. The patient experienced early miscarriage on 20Feb2021 with outcome of recovered. The patient had unknown very early pregnancy - vaccination around 4 weeks pregnant, miscarriage 2 weeks later. The patient underwent lab tests and procedures which included COVID-19 virus test: No - Negative COVID-19 test, scan: unknown result. Patient had 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: 1170729 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-20
Onset:2021-02-20
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 300042722 / 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? 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 (No medical history reported.)
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLMODERNATX, INC.MOD20210

Write-up: This regulatory authority prospective pregnancy case was reported by a consumer, concerning a 31 year old female patient who received mRNA-1273 for COVID-19 vaccination and describes the occurrence of miskraam (abortion spontaneous) and vaccinatie tijdens zwangerschap (Vaccine exposure during pregnancy). The patient''s past medical history was not reported. Concomitant medications were not reported. On 20 Feb 2021, prior to the onset of the symptoms, the patient received their first of two planned doses of mRNA-1273 (Batch number: 300042722) intramuscularly for prophylaxis of COVID-19 infection. Last menstrual period and estimated date of delivery were not provided. On 20 Feb 2021, patient experienced vaccine exposure during pregnancy week 4, and on 02 Mar 2021 the patient experienced a miscarriage. Action taken with mRNA-1273 in response to the events was reported as not applicable. The outcome of the event, miskraam (spontaneous abortion), was unknown/not reported. The outcome of the event, Vaccinatie tijdens zwangerschap (vaccine exposure during pregnancy), was considered resolved on 20 Feb 2021.; Reporter''s Comments: This report concerns a 31-year-old female patient with who was administered mRNA-1273 while pregnant (vaccine exposure during pregnancy) (Batch #r: 300042722) and experienced abortion 10 days post administration of mRNA-1273. There is not enough information regarding this case as medical, obstetric, gynecological history and clinical details of abortion are lacking. The event of vaccine exposure during pregnancy is assessed as not applicable. No further information is expected.; Sender''s Comments: Since the nature of the reported reaction does imply seriousness according to one of the critera, the reaction was considered as serious.


VAERS ID: 1328185 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-12
Onset:2021-02-20
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-05-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK4244 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure during pregnancy, Scan, 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? 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 (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Date: 20210220; Test Name: Scan; Result Unstructured Data: Test Result:Pregnancy non viable at 6 weeks; Test Name: NHS scan; Result Unstructured Data: Test Result:Unknown results
CDC Split Type: GBPFIZER INC2021493061

Write-up: Maternal exposure during pregnancy; Miscarriage; This is a spontaneous report from a contactable consumer received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202104301509048940-FFAE6, Safety Report Unique Identifier is GB-MHRA-ADR 25225505. A 32-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 12Feb2021 (Batch/Lot Number: EK4244) as single dose for covid-19 immunisation. Medical history included pregnancy from an unknown date (patient no longer pregnant at the time of reporting). Concomitant medication included folic acid (FOLIC ACID) taken for vitamin supplementation, start and stop date were not reported. The patient experienced miscarriage on 20Feb2021 and maternal exposure during pregnancy on an unspecified date. Patient was exposed to the medicine first-trimester (1-12 weeks). It was reported that pregnancy suspected to have miscarried around 20Feb2021 and physical miscarriage happened around 18March2021. The events were assessed as non-serious by the regulatory authority. The patient underwent lab tests and procedures which included scan with pregnancy non-viable at 6 weeks (approximately 20Feb2021) and ultrasound scan with unknown results on an unspecified date. The patient recovered from miscarriage on 18Mar2021 while outcome for maternal exposure during pregnancy was unknown. No follow up attempts are possible. No further information is expected.


VAERS ID: 1066049 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: North Dakota  
Vaccinated:2021-01-06
Onset:2021-02-21
   Days after vaccination:46
Submitted: 0000-00-00
Entered: 2021-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 027L20A / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound antenatal screen
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: prenatal vitamins
Current Illness: none
Preexisting Conditions: none
Allergies: NKA
Diagnostic Lab Data: Ultra sound confirmed but dates not reported. No medical intervention reportedly needed to complete miscarriage.
CDC Split Type:

Write-up: Reported by patient to have been 9.5weeks pregnant when miscarriage happened.


VAERS ID: 1243908 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-02-02
Onset:2021-02-21
   Days after vaccination:19
Submitted: 0000-00-00
Entered: 2021-04-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL8982 / 2 LA / -

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? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: 10mg Lexapro and prenatal vitamins
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Surgical D&C
CDC Split Type:

Write-up: I was 4 weeks pregnant at the time of my second dose. I miscarried at around 7weeks 6 days. It was suggested due to potential Triploidy but I thought it would be informative that you know.


VAERS ID: 1527152 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Florida  
Vaccinated:2021-02-18
Onset:2021-02-21
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-08-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / SYR

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? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Excedrin as needed for headaches
Current Illness: None
Preexisting Conditions: Migraines
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Vaccine was administered on 2/18, started vaginal spotting on 2/19-2/20 and suffered a miscarriage on 2/21 at five weeks and six days pregnant.


VAERS ID: 1778962 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: New York  
Vaccinated:2021-02-18
Onset:2021-02-21
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 015M20A / 2 LA / -

Administered by: Other       Purchased by: ?
Symptoms: Adverse event, Exposure during pregnancy, Malaise, Pain, Premature delivery, Premature labour, Pyrexia, Uterine contractions during pregnancy, Uterine hypertonus
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Normal pregnancy conditions and outcomes (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (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? Yes, 3 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Folic Acid
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data:
CDC Split Type:

Write-up: I was 7 months pregnant at the time that I was taking my second dose of the Covid-19 Vaccine. My due date was April 20th. On Thursday, February 18th I got my 2nd dose. That morning, I had been checked by my doctor and had a 32 sonogram and everything was deemed healthy. On Friday, I felt achy and had slight fever- I attributed it to the vaccine and took it easy that day, resting. On Saturday, I was still achy. I also started having Braxton hicks contractions (or so I thought) around 12 pm. I was achy and not feeling well all day and again attributed that to the vaccine. Early Sunday morning (2/21) around 12:30 am, I realized that my braxton hicks contractions were increasing and getting worse. By the time I realized I was in labor it was 2 am. We rushed to the hospital and I had my son at 32 weeks. The adverse event is that I gave birth 8 weeks early and that my son had to spend 2 weeks in the NICU just days after receiving my second dose. (In my previous two pregnancies, my body had never gone into labor itself. I had to be induced.)


VAERS ID: 1106964 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-21
Onset:2021-02-21
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-03-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6134 / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Intermenstrual bleeding, Ultrasound scan
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? 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: Pregnancy (Date of the last menstrual period: 06/014/2021. On 17Feb2021 ultrasound evaluation confirming six-week gestation (intrauterium gestational sac 10x5 mm without embryonic complex))
Allergies:
Diagnostic Lab Data: Test Date: 20210217; Test Name: Echography; Test Result: Positive
CDC Split Type: ESPFIZER INC2021222099

Write-up: Spontaneous abortion; Metrorrhagia; This is a spontaneous report from a contactable consumer downloaded from the Regulatory Authority ES-AEMPS-764672. A 34-years-old female patient received bnt162b2 (COMIRNATY, lot number EJ6134), intramuscular on 21Feb2021 at a single dose for Covid-19 immunisation. Medical history included pregnancy from Jan2021 (Last menstrual period: reported as 06/014/2021). On 17Feb2021 ultrasound evaluation confirming six-week gestation (intrauterim gestational sac 10x5 mm without embryonic complex). The patient''s concomitant medications were not reported. On 21Feb2021, the patient experienced spontaneous abortion and metrorrhagia. The mother reported she became pregnant while taking bnt162b2. The pregnancy resulted in spontaneous abortion. The patient underwent ultrasound evaluation confirming six-week gestation (intrauterium gestational sac 10x5 mm without embryonic complex) on 17Feb2021. Outcome of the events of metorrhagia was recovered, while spontaneous abortion was unknown. The events were considered serious and medically significant by regulatory authority. Comments: Date of the last menstrual period: 06/014/2021. On 17Feb2021 ultrasound evaluation confirming six-week gestation (intrauterium gestational sac 10x5 mm without embryonic complex) No follow-up attempts possible. No further information expected.


VAERS ID: 1260398 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-16
Onset:2021-02-21
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-04-26
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, Scan, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? Yes
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: Test Date: 20210221; Test Name: COVID-19 virus test; Test Result: Negative ; Test Name: 12 week scan; Result Unstructured Data: Test Result:seeming to be well at my 12 week scan
CDC Split Type: GBPFIZER INC2021437831

Write-up: Miscarriage of pregnancy; Hemorrhage vaginal; This is a spontaneous report from a contactable consumer(patient) received from The regulatory authority report number is GB-MHRA-WEBCOVID-202104191303576540. The female patient of an unspecified age received BNT162B2, dose 1 via an unspecified route of administration on 16Feb2021 (Lot Number: Not known) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient had not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. She became pregnant while taking bnt162b2. The patient experienced miscarriage of pregnancy on 21Feb2021 with outcome of recovered on 21Feb2021 , hemorrhage vaginal on 21Feb2021 with outcome of recovered with sequelae in 2021. The events led to hospitalization, life threatening. It was stated that she received the pfizer vaccine on the 16th of February currently pregnant with everything seeming to be well at her 12 week scan a few weeks previous. 5 days later on the 21st(on 21Feb2021) she woke up to blood pouring from her. She was hemorrhaging and she lost her baby at 17 weeks gestation. Lab data also included COVID-19 virus test: negative on 21Feb2021. Patient had 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: 1054826 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Michigan  
Vaccinated:1921-01-25
Onset:2021-02-22
   Days after vaccination:36553
Submitted: 0000-00-00
Entered: 2021-02-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3248 / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Brain injury, Foetal exposure during pregnancy, Premature baby, Premature delivery, Premature labour, Ultrasound skull
SMQs:, Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Neonatal disorders (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: Pre natal vit, Zofran, pepcid
Current Illness: Depression, bipolar, anxiety, panic attacks, migraines, asthma, gestational diabetes
Preexisting Conditions: Depression, bipolar, anxiety, panic attacks, migraines, asthma
Allergies: NKA
Diagnostic Lab Data: Crainial ultrasound 2-22-21
CDC Split Type:

Write-up: Premature infant born at hospital after premature labor was found to have injured brain tissue (PVL) on cranial ultrasound after delivery. Timing of the injury coincides with maternal clinical illness after second Covid vaccine, about two weeks prior to delivery. The mother and father asked me whether the Covid vaccine could have contributed to the brain injury. I reassured them that the Covid vaccine is felt to be safe during pregnancy, but that I would report the concern.


VAERS ID: 1090217 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-02-04
Onset:2021-02-22
   Days after vaccination:18
Submitted: 0000-00-00
Entered: 2021-03-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9269 / 1 LA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Heart rate, Investigation, Laboratory test, Ultrasound scan
SMQs:, 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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: VITAMIN D; FOLATE; ZOLOFT
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Penicillin allergy
Allergies:
Diagnostic Lab Data: Test Date: 20210203; Test Name: heartbeat; Result Unstructured Data: Test Result:152 bpm; Test Date: 20210220; Test Name: heartbeat; Result Unstructured Data: Test Result:no heartbeat detected; Test Date: 20210203; Test Name: hormone levels; Result Unstructured Data: Test Result:normal ranges. No issues detected.; Test Date: 20210203; Test Name: OB exam; Result Unstructured Data: Test Result:showed healthy baby at 7w5d; Test Date: 20210203; Test Name: Labs; Result Unstructured Data: Test Result:normal ranges. No issues detected.; Test Date: 20210203; Test Name: ultrasound; Result Unstructured Data: Test Result:no abnormalities identified; Test Date: 20210220; Test Name: ultrasound; Result Unstructured Data: Test Result:fetus stopped growing on 09Feb21 (8w4d)
CDC Split Type: USPFIZER INC2021204433

Write-up: Miscarriage; This is a Spontaneous report from a contactable consumer (patient). This consumer reported information for both mother and fetus. This is the maternal report. A 39-year-old female consumer reported that a 39-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number: EL9269), via an unspecified route of administration at left arm on 04Feb2021 14:00 at a single dose for COVID-19 immunization. Medical history included allergies: Penicillin. No other vaccine in four weeks. Concomitant medications included (in two weeks) Prenatal vitamin, colecalciferol (VITAMIN D), folic acid (FOLATE) and sertraline hydrochloride (ZOLOFT 25mg). The patient''s last menstrual date was 14Dec2020 and the delivery date was on 17Sep2021 (Gestational period: 8, as reported). An OB exam on 03Feb2021 showed healthy baby at 7w5d- heartbeat detected 152bpm; no abnormalities identified via ultrasound, Labs and hormone levels all within normal ranges. No issues detected. Mother received 1st dose of vaccine 04Feb2021. Per ultrasound on 20Feb2021, fetus stopped growing on 09Feb2021 (8w4d); no heartbeat detected. Miscarriage occurred 22Feb2021. AE resulted in Emergency room/department or urgent care, congenital anomaly (as reported). No treatment was administered. No COVID prior vaccination. Patient not COVID tested post vaccination. The outcome of the event was not recovered.; Sender''s Comments: Linked Report(s) : US-PFIZER INC-2021225027 fetus case


VAERS ID: 1096573 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-01-21
Onset:2021-02-22
   Days after vaccination:32
Submitted: 0000-00-00
Entered: 2021-03-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / -

Administered by: Private       Purchased by: ?
Symptoms: Caesarean section, Exposure during pregnancy, Haemorrhage in pregnancy, Premature delivery, Premature labour, Premature separation of placenta
SMQs:, Haemorrhage terms (excl laboratory terms) (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? No
Hospitalized? Yes, 4 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: I was taking a prenatal vitamin.
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data: No
CDC Split Type: vsafe

Write-up: I went into labor during which I started bleeding and was rushed into have an emergency C-section. I had a placenta abruption. Both mom and baby are doing fine. Estimated due date was 03/01/2021. Birth weight was 6 lbs 14 oz


VAERS ID: 1096812 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Kansas  
Vaccinated:2021-02-03
Onset:2021-02-22
   Days after vaccination:19
Submitted: 0000-00-00
Entered: 2021-03-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 RA / SYR

Administered by: Military       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Exposure during pregnancy, Platelet count increased
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? No
Previous Vaccinations:
Other Medications: Zyrtec
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Blood work- platelet blood count elevated
CDC Split Type: vsafe

Write-up: After my second dose I had a miscarriage but it was identified on 02/22/2021, I was 11 weeks pregnant and I had no complications with my pregnancy, Before my 1st dose my platelet blood count was at 400 then after my 1st dose it went to 538.


VAERS ID: 1201409 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: Tennessee  
Vaccinated:2020-12-21
Onset:2021-02-22
   Days after vaccination:63
Submitted: 0000-00-00
Entered: 2021-04-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0140 / 2 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Exposure during pregnancy, Premature labour, Stillbirth, Thrombosis
SMQs:, 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? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Phenergan, dicylegis
Current Illness: No
Preexisting Conditions: None
Allergies: Neosporin
Diagnostic Lab Data: Placenta sent for pathology - 2 blood clots. No infectious source.
CDC Split Type:

Write-up: Delivered preterm infant (stillbirth) at 24 weeks on March 9, 2021. Infant had IUGR noted at 19 weeks. Placenta showed 2 blood clots restricting blood flow at delivery. Mother with no known clotting disorders. 2 prior healthy infants.


VAERS ID: 1328511 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-12
Onset:2021-02-22
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-05-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN 6201 / 2 RA / IM

Administered by: Private       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? 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:
CDC Split Type:

Write-up: Found out I was pregnant Feb 11th, 2021, the day before my second dose of covid-19 vaccination. Started bleeding February 22nd, 2021. Went to Emergency Room and was informed may be having a miscarriage. Persisted bleeding for a week. Visited an OB throughout that week and verified I was going through a miscarriage and was approximately 4-5 weeks. First pregnancy and only pregnancy.


VAERS ID: 1755601 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Guam  
Vaccinated:2021-01-25
Onset:2021-02-22
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-10-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029L20A / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Emotional distress, Heavy menstrual bleeding, Ultrasound scan abnormal
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Malignancy related therapeutic and diagnostic procedures (narrow), Depression (excl suicide and self injury) (broad), 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: Sulfa
Diagnostic Lab Data: Miscarriage, 02/22/2021 She received only first dose of Moderna vaccine. FIRST TRIMESTER MISCARRIAGE CONFIRMED POST VACCINE BY ULTRASOUND AND Beta HCG. Patient is recovering from physical and emotional trauma. Will continue to follow.
CDC Split Type:

Write-up: LMP 12/12/2020 first dose moderna vaccine one 1/25/2021 patient states heavy vaginal bleeding on 2/22/2021


VAERS ID: 1176385 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-12
Onset:2021-02-22
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 300042722 / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion
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: No adverse event
Allergies:
Diagnostic Lab Data:
CDC Split Type: ESMODERNATX, INC.MOD20210

Write-up: Abortion; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 25-Mar-2021 and was forwarded to Moderna on 25-Mar-2021. This regulatory authority case was reported by a physician (subsequently medically confirmed) and describes the occurrence of ABORTION (Abortion) in a 34-year-old female patient who received mRNA-1273 (COVID 19 Vaccine Moderna) (batch no. 300042722) for COVID-19 vaccination. The patient''s past medical history included No adverse event. On 12-Feb-2021, the patient received first dose of mRNA-1273 (COVID 19 Vaccine Moderna) (Intramuscular) 1 dosage form. On 22-Feb-2021, after starting mRNA-1273 (COVID 19 Vaccine Moderna), the patient experienced ABORTION (Abortion) (seriousness criterion medically significant). On 22-Feb-2021, ABORTION (Abortion) had resolved. The action taken with mRNA-1273 (COVID 19 Vaccine Moderna) (Intramuscular) was unknown. For mRNA-1273 (COVID 19 Vaccine Moderna) (Intramuscular), the reporter did not provide any causality assessments. This is a case of product exposure during pregnancy and abortion for this 34-year-old female. Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded Reporter did not allow further contact; Sender''s Comments: This is a case of product exposure during pregnancy and abortion for this 34-year-old female. Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded


VAERS ID: 1185846 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-12
Onset:2021-02-22
   Days after vaccination:41
Submitted: 0000-00-00
Entered: 2021-04-09
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: Breast feeding (1 healthy 2 years old)
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage (Details of previous pregnancies: 1 previous 1st trimester miscarriage); Pregnancy (previous pregnancies:1 healthy 2 years old Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021334270

Write-up: Miscarriage; This is a spontaneous report from a contactable physician received from the Regulatory Agency (RA). Regulatory authority report number (GB-MHRA-WEBCOVID-202103242303585520), Safety Report Unique Identifier (GB-MHRA-ADR 25016582). A 37-year-old female patient received bnt162b2 (Pfizer-BioNTech COVID-19 vaccine), dose 1 via an unspecified route of administration on 12Jan2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient''s medical history included previous pregnancies: 1 previous 1st trimester miscarriage and 1 healthy 2 years old (Patient no longer pregnant at the time of reporting); and ongoing breast feeding (1 healthy 2 years old). Patient has not had symptoms associated with COVID-19 Patient is not enrolled in clinical trial. Concomitant medication included folic acid taken for folic acid supplementation, start and stop date were not reported. On 22Feb2021, the patient experienced miscarriage. The event was reported as serious, seriousness criteria-other medically important condition. The reporter was unsure if the product has an adverse effect on any aspect of the pregnancy. Patient was exposed to the product on first-trimester (1-12 weeks). She was vaccinated on 12Jan2021, and was diagnosed "missed miscarriage" (as reported) on 22Feb2021. The mother was 10 Weeks pregnant at the onset of the event. The mother was due to deliver on Sep2021. The pregnancy resulted in spontaneous abortion. The patient underwent lab tests and procedures which included COVID-19 virus test on an unspecified date: No - Negative COVID-19 test. The outcome of the event was recovered (in 2021). 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: 1070952 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Nebraska  
Vaccinated:2020-12-21
Onset:2021-02-23
   Days after vaccination:64
Submitted: 0000-00-00
Entered: 2021-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: 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? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, magnesium, fluoxetine, Allegra, nexium, unisom
Current Illness: N/a
Preexisting Conditions: Chronic migraine , iron deficiency anemia
Allergies: Allergies to penicillin and the nuva ring.
Diagnostic Lab Data: N/a
CDC Split Type:

Write-up: I was not pregnant at the time of the first vaccine, but was pregnant at the time of the second vaccine. I had a miscarriage on 2/24/2021


VAERS ID: 1096971 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Arizona  
Vaccinated:2021-02-20
Onset:2021-02-23
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-03-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 RA / -

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Haemorrhage, Laboratory test
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (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: I was taking prenatal vitamins, a probiotic, vitamin D and magnesium.
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data: Labs were drawn about a week later looking for HCG.
CDC Split Type: vsafe

Write-up: I had abdominal pain and bleeding. I suffered a miscarriage.


VAERS ID: 1636857 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Arkansas  
Vaccinated:2021-01-12
Onset:2021-02-23
   Days after vaccination:42
Submitted: 0000-00-00
Entered: 2021-08-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL 1284 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Ectopic pregnancy, Exposure during pregnancy, Foetal heart rate abnormal, Human chorionic gonadotropin, Ultrasound foetal abnormal, Vaginal haemorrhage
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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin Zoloft
Current Illness: None
Preexisting Conditions: Anxiety
Allergies: Amoxicillin
Diagnostic Lab Data: Multiple beta HCG labs & ultrasounds.
CDC Split Type:

Write-up: Positive pregnancy test 01/01/2021; Vaginal spotting, no fetal heart tones found at first OB appointment, 01/18/2021. No fetal heart tones at follow up appointment on 02/04/2021. No fetal heart tones found 02/22/2021. Tissue passed resulting in confirmed miscarriage 02/23/2021. Est delivery date 09/2021. Following ectopic pregnancy diagnosed 05/07/2021. 1 living child born 02/2018 at 37 weeks gestation r/t preeclampsia; no other pregnancy complications.


VAERS ID: 1153650 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-16
Onset:2021-02-23
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-04-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER0641 / 2 LA / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Human chorionic gonadotropin, 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:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnancy (carried to term with delivery in Mar2020)
Allergies:
Diagnostic Lab Data: Test Date: 20210119; Test Name: blood beta Hcg; Test Result: Negative ; Test Date: 20210120; Test Name: PCR test; Test Result: Negative
CDC Split Type: FRPFIZER INC2021272485

Write-up: Miscarriage; This is a spontaneous report from contactable physician downloaded from the Regulatory Authority-WEB FR-AFSSAPS-AN20210656. A 32-year-old female patient received the second dose of bnt162b2 (COMIRNATY, Lot Number: ER0641), intramuscular in left arm on 16Feb2021 at a single dose for COVID-19 immunization. The patient''s medical history included pregnancy carried to term with delivery in Mar2020. The patient was not at risk of developing a severe form of the COVID-19 disease. No history of COVID-19. History of allergy/hypersensitivity was unknown. Concomitant medications were not reported. Patient vaccinated with the first dose of Comirnaty on 22Jan2021 (lot number: EJ6788) for COVID-19 immunization. Interval between two injections was 25 days. The patient reported that her last menstrual period was on 17Dec2020, first dose at 5 weeks of amenorrhoea but dating the start of the pregnancy difficult because of irregular cycles since her periods returned, negative blood beta human chorionic gonadotropinon (beta Hcg) on 19Jan2021 therefore likely that the pregnancy started in between the 2 injections (First dose of Comirnaty at 5 weeks of gestation). Otherwise, no generalised signs or fever following the 2 doses. The patient presented with a miscarriage on 23Feb2021, one week after a second dose of Comirnaty. The patient was not aware that she was pregnant at the time of the vaccination. The patient became pregnant while taking bnt162b2. The patient was due to deliver on 23Sep2021. The pregnancy resulted in spontaneous abortion. The patient underwent lab tests and procedures which included human chorionic gonadotropin: negative on 19Jan2021 and COVID-19 test: Negative PCR on 20Jan2021. Treatment and development included medical consultation (as reported). The outcome of the event was recovered on unspecified date in 2021. (NB: Accountability "without prejudice to further investigations that could be carried out as part of legal or amicable compensation procedures." No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : FR-PFIZER INC-2021341637 same patient/different dose


VAERS ID: 1171951 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-01
Onset:2021-02-23
   Days after vaccination:53
Submitted: 0000-00-00
Entered: 2021-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0203 / 1 LA / -

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: Concussion; In vitro fertilisation
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAPFIZER INC2021312720

Write-up: miscarriage; This is a spontaneous report from a contactable physician (patient) via COAVES. A 35-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration, administered in arm left on Jan2021 (Batch/Lot Number: EL0203) as single dose for covid-19 immunisation. Medical history included concussion from an unknown date and unknown if ongoing, and pregnancy was with IVF and her transfer date was 03Jan2021, day 5 embryo. The patient''s concomitant medications included unspecified medications. The patient experienced miscarriage on 23Feb2021. The mother reported she became pregnant while taking bnt162b2. The mother was 8 Weeks pregnant at the onset of the event. The mother was due to deliver on 21Sep2021. The pregnancy resulted in spontaneous abortion. The patient recovered from the event on an unspecified date. The patient was not diagnosed with COVID-19 prior to vaccination and has not been tested for COVID-19 since the vaccination.; Sender''s Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of event Miscarriage cannot be totally excluded. The case will be reassessed if 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: 1173200 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-23
Onset:2021-02-23
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / 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? 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: SALOSPIR
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Smoker (she did not smoke during pregnancy); Spontaneous abortion
Allergies:
Diagnostic Lab Data:
CDC Split Type: GRPFIZER INC2021311594

Write-up: Spontaneous abortion; The patient was not aware of her pregnancy during the vaccination; The patient was not aware of her pregnancy during the vaccination; This is a spontaneous report from a contactable pharmacist downloaded from the WEB GR-GREOF-20211824. A 33-year-old female patient received bnt162b2 (COMIRNATY), intramuscularly on 23Feb2021 as single dose for COVID-19 immunisation. Medical history included spontaneous abortion from 2019 to 2019 and smoker but clarified that she did not smoke during pregnancy. Concomitant medication included acetylsalicylic acid (SALOSPIR). It was reported that the patient was not aware of her pregnancy during the vaccination on 23Feb2021. It was also reported that the patient experienced spontaneous abortion on 15Mar2021. The seriousness of event spontaneous abortion was reported as congenital anomaly. The mother was 3 weeks pregnant at the onset of the event and was due to deliver on 10Nov2021. Outcome of event was not recovered. No follow up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1114382 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Texas  
Vaccinated:2021-02-20
Onset:2021-02-24
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9266 / 2 LA / OT

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal death
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? Yes
   Date died: 2021-02-24
   Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021278790

Write-up: Baby stop growing 3 days later (7 weeks 3 days per sono); Baby stop growing 3 days later (7 weeks 3 days per sono); This is a spontaneous report from a contactable Other HCP. This Other HCP reported events for herself and fetus. This is a fetus report. A 40-year-old mother received bnt162b2 (BNT162B2), dose 2 administered in Arm Left on 20Feb2021 (Batch/Lot Number: El9266) as SINGLE DOSE, dose 1 administered in Arm Left on 27Jan2021 (Batch/Lot Number: El3248) as SINGLE DOSE for covid-19 immunisation. The mother medical history included allergies: Shellfish. No other vaccine in four weeks. No COVID prior vaccination. Concomitant medication 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). The mother was pregnant. Last menstrual date: 04Jan2021. Due Date: 11Oct2021. The mother was 7 weeks pregnant at time of 2nd vaccine. Baby stop growing 3 days later (7 weeks 3 days per sono) on 24Feb2021 08:00 AM. AE resulted in: Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. The patient died on 24Feb2021 08:00 AM. It was not reported if an autopsy was performed.; Sender''s Comments: Based on provided information and temporal association the reported events causal relationship with the suspect drug cannot be excluded. However there is very limited information provided in this report. Additional information is needed to better assess the case, including complete medical history and diagnostics workup. This case will be reassessed upon receipt of follow-up information. 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-2021277400 Same reporter/drug, different patient /event (mother case); Reported Cause(s) of Death: Baby stop growing 3 days later (7 weeks 3 days per sono); Baby stop growing 3 days later (7 weeks 3 days per sono)


VAERS ID: 1151400 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-02-20
Onset:2021-02-24
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-03-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9266 / 2 LA / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion induced, Maternal exposure during pregnancy, Off label use, Product use issue, 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), Medication errors (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? No
Previous Vaccinations:
Other Medications: PRENATAL VITAMINS [ASCORBIC ACID;CALCIUM PANTOTHENATE;CYANOCOBALAMIN;ERGOCALCIFEROL;NICOTINAMIDE;PYR
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Shellfish allergy
Allergies:
Diagnostic Lab Data: Test Date: 20210312; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Unknown results
CDC Split Type: USPFIZER INC2021277400

Write-up: I was 7 weeks pregnant at time of 2nd vaccine. Baby stop growing 3 days later (7 weeks 3 days per sono); I was 7 weeks pregnant at time of 2nd vaccine. Baby stop growing 3 days later (7 weeks 3 days per sono; I was 7 weeks pregnant at time of 2nd vaccine. Baby stop growing 3 days later (7 weeks 3 days per sono; I was 7 weeks pregnant at time of 2nd vaccine. Baby stop growing 3 days later (7 weeks 3 days per sono; This is a spontaneous report from a contactable Other HCP reported for herself and fetus. This is mother case. A 40-year-old pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: El9266), via an unspecified route of administration on Left arm on 20Feb2021 08:00 at single dose for covid-19 immunisation administered at Hospital. Medical history includes Shellfish Allergy. Historical vaccine includes first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: El3248), via an unspecified route of administration on Left arm on 27Jan2021 09:30 at single dose for covid-19 immunisation. Concomitant medications in two weeks include ascorbic acid, calcium pantothenate, cyanocobalamin, ergocalciferol, nicotinamide, pyridoxine hydrochloride, retinol palmitate, riboflavin, thiamine mononitrate (PRENATAL VITAMINS). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient reported, she was 7 weeks pregnant at time of 2nd vaccine. Baby stop growing 3 days later (7 weeks 3 days per sono) on 24Feb2021 08:00 on visit of Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. The patient received Dilation and curettage (D&C) treatment for the events. Last menstrual date was 04Jan2021. Delivery date is Oct2021. Gestational period was 7 weeks. Prior to vaccination, was the patient was not diagnosed with COVID-19. The patient had COVID tested/nasal swab post vaccination with results pending on12Mar2021. The outcome of event Miscarriage was resolving and for the other events it was unknown. Follow-up attempts are completed. No further information is expected.; Sender''s Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of event Induced abortion cannot be excluded. The case will be reassessed if 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.,Linked Report(s) : US-PFIZER INC-2021278790 Same reporter/drug, different patient /event (Fetus case)


VAERS ID: 1396622 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-01-07
Onset:2021-02-24
   Days after vaccination:48
Submitted: 0000-00-00
Entered: 2021-06-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1283 / 2 RA / 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? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zyrtec, pre-natal vitamins
Current Illness: None reported
Preexisting Conditions: None reported
Allergies: None reported
Diagnostic Lab Data:
CDC Split Type: vsafe

Write-up: At the beginning of January, my husband and I had already been trying to conceive. I received my second dose vaccine on 01-07-2021. In the first week of February I found out I was pregnant. By the end of February I had a miscarriage. I had the miscarriage on 02-24-2021. The day I miscarried I was going to have my first gynecological appointment to check my baby. I do not know if the vaccine had anything to do with my miscarriage. I was hesitant to getting my second dose but I still went through with it. I just think it is important for mothers who are expecting to wait at least till their second trimester to receive the Covid 19 vaccine, my opinion.


VAERS ID: 1754949 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Guam  
Vaccinated:2021-02-08
Onset:2021-02-24
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-10-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011120A / 1 LA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 02211120A / 2 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Human chorionic gonadotropin, Maternal 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? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Vit-C
Current Illness: None
Preexisting Conditions: None
Allergies: Acetaminophin and various fever drugs
Diagnostic Lab Data: FIRST TRIMESTER MISCARRIAGE CONFIRMED POST VACCINE BY ULTRASOUND AND Beta HCG. Patient is recovering from physical and emotional trauma. Will continue to follow.
CDC Split Type:

Write-up: Miscarriage, 02/24/2021


VAERS ID: 1126485 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-07
Onset:2021-02-24
   Days after vaccination:48
Submitted: 0000-00-00
Entered: 2021-03-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM0477 / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed, Gynaecological examination, 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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: GIONA; FLIXONASE; SINGULAIR; BUVENTOL EASYHALER
Current Illness: Asthma; Runny nose
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnancy NOS
Allergies:
Diagnostic Lab Data: Test Date: 2021; Test Name: Gynaecological examination; Result Unstructured Data: Test Result:No results available
CDC Split Type: DKPFIZER INC2021249351

Write-up: Maternal exposure during pregnancy; Missed abortion; This is a spontaneous report downloaded from the regulatory authority number (DK-DKMA-WBS-0045438) and Sender''s (Case) Safety Report Unique Identifier (DK-DKMA-ADR 24856559). A contactable physician reported that a 33-year-old female patient (pregnant) received the first dose of BNT162B2 (COMIRNATY, Solution for injection, lot number: EM0477), via an unspecified route of administration on 07Jan2021 (at the age of 33 years old and pregnant) at a single dose for COVID-19 immunization. The patient''s medical history included asthma and runny nose, both ongoing; unknown pregnancy from an unknown date and not continue. Concomitant medication included budesonide (GIONA) (reported as GIONA EASYHALER) via resp inhalation from 12Jan2021 for asthma, fluticasone propionat (FLIXONASE) via nasal from 29Oct2019 to 25Feb2021 for runny nose, montelukast natrium (SINGULAIR) orally from 11Nov20216 for asthma, salbutamol sulfat (BUVENTOL EASYHALER) via resp inhalation from 27Jan2020 for asthma. The patient experienced maternal exposure during pregnancy on an unspecified date which was considered caused hospitalization, missed abortion on 24Feb2021 which was considered caused hospitalization. The physician describes the occurrence of missed abortion in a 33 years old female patient, vaccinated with COMIRNATY (TOZINAMERAN). There was no information regarding past medication. On 07Jan2021 the patient was vaccinated with first dose of Comirnaty (EM0477) for COVID-19 immunisation. On 24Jan2021 the patient was diagnosed with Missed abortion. The ADR were by the physician reported as resulting in hospitalisation. No treatment due to the ADR was reported. The patient underwent lab tests and procedures which included gynaecological examination: no results available in 2021. The outcome of event "missed abortion" was not recovered. The outcome of other event was recovered. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1149579 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-08
Onset:2021-02-24
   Days after vaccination:47
Submitted: 0000-00-00
Entered: 2021-03-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6796 / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion induced, Foetal heart rate
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: Fertility female decreased (Fertility problems)
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210224; Test Name: fetal heartbeat; Result Unstructured Data: Test Result:lack of fetal heartbeat; Comments: suffered an induced abortion due to lack of fetal heartbeat
CDC Split Type: ESPFIZER INC2021283153

Write-up: Abortion induced due to lack of fetal heartbeat; This is a spontaneous report from a contactable other healthcare professional downloaded from the Regulatory Authority (regulatory authority report number: ES-AEMPS-784906). This other healthcare professional reported information for both mother and fetus. This is the maternal report. A 38-year-old female patient received BNT162B2 (COMIRNATY, Solution for injection, lot number: EJ6796), via an unspecified route of administration, 08Jan2021 at a single dose for COVID-19 immunization. Medical history included ongoing fertility problems. Date of LMP (last menstrual period) was 16Dec2021. Gestation Period at Exposure was at 3 weeks. Concomitant medications was not reported. The patient with fertility problems was vaccinated with BNT162B2 on 08Jan2021 without knowing she was pregnant. She suffered an induced abortion due to lack of fetal heartbeat on 24Feb2021, at 10 weeks of gestation (reported as 9 weeks of gestation). Outcome of the event was recovered on 24Feb2021. No follow-up attempts are possible, no information is expected.


VAERS ID: 1308552 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-23
Onset:2021-02-24
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER1471 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Stillbirth
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? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: EMPAGLIFLOZIN; METFORMIN
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Diabetes; Maturity-onset diabetes of the young
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021469129

Write-up: Stillbirth; This is a spontaneous report from a contactable physician. This is a report received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202104261643109810-TBN2H, and Safety Report Unique Identifier is GB-MHRA-ADR 25199110. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 23Feb2021 (lot number: ER1471) as 1st dose, single for COVID-19 immunisation. Medical history included maturity-onset diabetes of the young (MODY), and diabetes. Patient was pregnant at the time of vaccination. Unsure if patient has had symptoms associated with COVID-19. Patient has not had a COVID-19 test; and unsure if patient is enrolled in clinical trial. Concomitant medications included empagliflozin taken for diabetes mellitus from 2016; and metformin taken for diabetes mellitus from 08Jan2014. The patient experienced stillbirth on 24Feb2021 with outcome of recovered on 24Feb2021. The event was assessed by health authority as serious, congenital anomaly. It was reported that patient had the vaccine, then still birth the following day, dealt with at hospital name. Unsure if associated. Patient has not tested positive for COVID-19 since having the vaccine. No follow up attempts are possible. No further information is expected.


VAERS ID: 1312657 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-24
Onset:2021-02-24
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP2163 / 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? 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: SEPFIZER INC2021478439

Write-up: Miscarriage of pregnancy; MATERNAL EXPOSURE DURING PREGNANCY; This is a spontaneous report from a contactable consumer downloaded from the Regulatory Authority SE-MPA-2021-029274 received via regulatory authority. This is the first of two reports, 2nd vaccination dose. A 31-year-old female patient received the 2nd dose of bnt162b2 (COMIRNATY, lot number: EP2163) via an unspecified route of administration on 24Feb2021 at the same age at single dose for covid-19 immunisation. Medical history and concomitant medications were unknown. The patient previously received the 1st dose of bnt162b2 (COMIRNATY, lot number: EP2163) on 22Jan2021 for covid-19 immunisation, experiencing maternal exposure during pregnancy. The patient experienced suspected adverse event: miscarriage of pregnancy. The date of the miscarriage is stated as 15Apr2021 in the report. The heart of the fetus stopped beating. The woman stated that the side effect was discovered in week 12 of pregnancy. Outcome of the events was reported as recovered. This report was assessed as serious, other medically important event. No follow-up attempts possible. No further information expected.; Sender''s Comments: Linked Report(s) : SE-PFIZER INC-2021513131 Same patient and suspect product/ different AE and vaccination dose (1st)


VAERS ID: 1061109 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-18
Onset:2021-02-25
   Days after vaccination:38
Submitted: 0000-00-00
Entered: 2021-02-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3302 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Human chorionic gonadotropin decreased, Ultrasound scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), 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? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamins , vitamin D, probiotics
Current Illness: none
Preexisting Conditions: none
Allergies: latex, tree nuts
Diagnostic Lab Data: My miscarriage was confirmed by decreasing HCG levels from 2/24/2021 to 2/26/2021 and by ultrasound.
CDC Split Type:

Write-up: I was pregnant when I received my second dose of the Covid-19 Pfizer vaccine. My first Covid 19 vaccine was administered 12/28/2020. I got pregnant on 12/31/2020, received my second dose on 01/18/2021 and miscarried on 2/25/2021. I have had two prior uncomplicated pregnancies, and have never experienced a miscarriage. I gave birth to my two daughters, one at 42 weeks and one at 40 weeks and 5 days. My EDD for the pregnancy that ended in a miscarriage was due 09/23/2021.


VAERS ID: 1082396 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-16
Onset:2021-02-25
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-03-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 037K20A / 1 LA / IM

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? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, levothyroxine
Current Illness: none
Preexisting Conditions: hypothyroidism, depression, prediabetes
Allergies: NKDA
Diagnostic Lab Data: Procedure on 3/8/21 for miscarriage management
CDC Split Type:

Write-up: Patient suffered a miscarriage about 9 days after getting a covid vaccine.


VAERS ID: 1106442 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Oklahoma  
Vaccinated:2021-02-24
Onset:2021-02-25
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-03-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Human chorionic gonadotropin decreased, 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), Fertility disorders (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: No
Preexisting Conditions: No
Allergies: Sulfa and Chlordexidine
Diagnostic Lab Data: HCG level checks until zero to confirm pregnancy loss.
CDC Split Type:

Write-up: Within 24 hour I began to bleed and ultimately had a complete miscarriage of baby. I was at 6 weeks, with 2 healthy children (3 1/2 and 1 1/2 years old) with no prior pregnancy issues or complications.


VAERS ID: 1136131 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-01-27
Onset:2021-02-25
   Days after vaccination:29
Submitted: 0000-00-00
Entered: 2021-03-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9261 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound uterus
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: Prenatal vitamins
Current Illness: none
Preexisting Conditions: Asthma
Allergies: Penicillin allergy
Diagnostic Lab Data: Ultrasound showed missed miscarriage
CDC Split Type:

Write-up: Miscarriage at 6 weeks


VAERS ID: 1175159 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-02-17
Onset:2021-02-25
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6201 / 2 RA / OT

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous
SMQs:, 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: ACYCLOVIR [ACICLOVIR]
Current Illness: Herpes simplex type II
Preexisting Conditions: Medical History/Concurrent Conditions: Sulfonamide allergy
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021314046

Write-up: miscarriage/spontaneous abortion; This is a spontaneous report from a contactable nurse. A 31-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular, administered in Arm Right on 17Feb2021 15:30 (Batch/Lot Number: EN6201) as SINGLE DOSE for covid-19 immunisation. Medical history included ongoing herpes simplex 2 and sulfa allergy. Patient previously received the first dose of bnt162b2 for covid-19 immunisation. Concomitant medication included acyclovir) taken for an unspecified indication, start and stop date were not reported. The mother was 7 Weeks pregnant at the onset of the event. The patient experienced miscarriage/spontaneous abortion on 25Feb2021 16:45. The patient was supposedly due to deliver on 18Oct2021. The with outcome of event was recovered with sequelae. No follow-up attempts are possible, information about batch/lot number has already been obtained.


VAERS ID: 1285973 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-02-25
Onset:2021-02-25
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ELI 1283 / 2 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed, Foetal heart rate abnormal, Ultrasound scan, Uterine dilation and curettage
SMQs:, 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, iron with Vit C
Current Illness: none
Preexisting Conditions: none
Allergies: NKDA
Diagnostic Lab Data: Patient had a D&C after the US. There were no complications from that. She then returned to (country).
CDC Split Type:

Write-up: Patient received dose 2/2 of Pfizer vaccine on 2/25/2021. She had an IUI procedure done in (country) on 12/14/2020, which was confirmed to be successful at her follow up OB/Gyn visit- then returned to (country) . Patient returned to (country) on Feb 8, 2021 for 10 week US and was found to have no fetal heart tone, missed spontaneous abortion at approximately 7w5d. This timing would draw into question the timing of the vaccine administration.


VAERS ID: 1180964 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-23
Onset:2021-02-25
   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 EJ6136 / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Investigation, Pelvic pain, Ultrasound scan
SMQs:, Termination of pregnancy and risk of abortion (narrow), Sexual dysfunction (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: Parity 1 (Gesture: 2, Parity 1); Thrombophilia (Spouse); Vaginal delivery (birth of a child at 38 weeks old male weighing 2600 g, in good health)
Allergies:
Diagnostic Lab Data: Test Date: 20210203; Test Name: Biometry; Result Unstructured Data: Test Result:cranio-caudal length 1mm; Comments: cranio-caudal length 1mm or ultrasound early pregnancy; Test Name: Vitality; Result Unstructured Data: Test Result:Cardiac activity not measurable today; Comments: Cardiac activity not measurable today (early). To control; Test Date: 20210225; Test Name: Ultrasound; Result Unstructured Data: Test Result:intrauterine pregnancy, visualized embryo; Comments: Gestational sac: intrauterine pregnancy, visualized embryo, size 7.7 mm, normally toned, diffuse trophoblast, no image of detachment or hematoma; around 5 WA + 1 day; Test Date: 20210311; Test Name: Ultrasound; Result Unstructured Data: Test Result:Spontaneous miscarriage; Comments: Spontaneous miscarriage with persistence of small, non-vascularized intracavitary debris
CDC Split Type: FRPFIZER INC2021317389

Write-up: Early miscarriage; Left pelvic pain; This is a spontaneous report from a contactable consumer or other non HCP downloaded from the Regulatory Authority-WEB , Regulatory Authority number: FR-AFSSAPS-BX20211879. A 33-year-old female patient received bnt162b2 (COMIRNATY), intramuscular on 23Feb2021 (Batch/Lot Number: EJ6136) as single dose for covid-19 immunisation. Medical history included Parity 1 (Gesture: 2, Parity 1) from an unknown date, vaginal delivery in 2018; birth of a child at 38 weeks old male weighing 2600 g, in good health. Family history included probable thrombophilia (spouse) from an unknown date and unknown if ongoing. The patient''s concomitant medications were not reported. The patient experienced early miscarriage on 11Mar2021 and mention of left pelvic pain on ultrasound on 25Feb2021. The mother reported she became pregnant while taking bnt162b2. The patient''s last menstrual period was on 13Jan2021; theoretical start date of pregnancy was on 27Jan2021. The mother was due to deliver on 20Oct2021. The patient underwent lab tests and procedures which included Ultrasound from 25Feb2021 at around 5 WA + 1 day: Gestational sac: intrauterine pregnancy, visualized embryo, size 7.7 mm, normally toned, diffuse trophoblast, no image of detachment or hematoma; Biometry: cranio-caudal length 1mm or ultrasound early pregnancy on 03Feb2021; Vitality: Cardiac activity not measurable today (early). To control. Ultrasound check on 11Mar2021: Spontaneous miscarriage with persistence of small, non-vascularized intracavitary debris. The patient recovered from early miscarriage on an unspecified date while the outcome of pelvic pain was unknown. No follow-up attempts possible. No further information expected.


VAERS ID: 1185715 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-09
Onset:2021-02-25
   Days after vaccination:47
Submitted: 0000-00-00
Entered: 2021-04-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EE8493 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, 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? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage; Pregnancy (Patient no longer pregnant at the time of reporting)
Allergies:
Diagnostic Lab Data: Test Name: Scan; Result Unstructured Data: Test Result:okay; Comments: at 5 weeks; Test Name: Scan; Result Unstructured Data: Test Result:okay; Comments: at 7 weeks; Test Date: 20210225; Test Name: Scan; Result Unstructured Data: Test Result:confirmed miscarriage; Comments: at 9 weeks
CDC Split Type: GBPFIZER INC2021304976

Write-up: Early miscarriage/Miscarriage; This is a spontaneous report received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202103181400514420, Safety Report Unique Identifier: GB-MHRA-ADR 24970026. A contactable consumer reported that a 31-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: EE8493; expiry date: not known), via an unspecified route of administration on 09Jan2021 at single dose for COVID-19 immunisation. Medical history included miscarriage from an unknown date; and pregnancy (Patient no longer pregnant at the time of reporting). Patient has not had symptoms associated with COVID-19. Not had a COVID-19 test. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Concomitant medication included folic acid taken for folic acid supplementation. The patient experienced early miscarriage/miscarriage on 25Feb2021. Patient was exposed to the medicine first-trimester (1-12 weeks). Details of scans or investigations: scans at 5 and 7 weeks and results were okay and scan at 9 weeks (25Feb2021) confirmed miscarriage. The patient recovered from the event on 11Mar2021. Regulatory authority assessed the event as serious for being medically significant. It was unsure if the medicine had an adverse effect on any aspect of the pregnancy. For RA No follow-up attempts are possible. No further information is expected.


VAERS ID: 1234412 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2021-02-25
Onset:2021-02-25
   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 EP9598 / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Foetal death, Foetal growth restriction
SMQs:, 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? 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 INC2021415432

Write-up: premature stop of growth/embryo measures only 4 mm while its gestational age should correspond to a size of 10 mm; Maternal EDP, first trimester; This is a spontaneous report received from a contactable physician. This physician reported information for both mother and fetus/baby. This is the fetus/baby report. The mother report is a report downloaded from the Regulatory Authority, FR-AFSSAPS-MA20210991. A fetus of an unspecified gender received BNT162B2 (COMIRNATY), transplacental as the mother received the first dose of BNT162B2 (COMIRNATY, lot number: EP9598), intramuscular, on 25Feb2021, as single dose, for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. It was reported that the mother "stopped pregnancy after the first dose of COMIRNATY". It was also reported that "She was vaccinated on 25Feb2021 at 25 days of amenorrhea. On 17Mar2021, the embryo measures 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 the same day." The outcome of the events was unknown. No follow-up attempts possible. No further information expected.; Sender''s Comments: Linked Report(s) : FR-PFIZER INC-2021369668 mother case


VAERS ID: 1823036 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-25
Onset:2021-02-25
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-10-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6790 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed
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: Maternal vaccine exposure (COVID-19 vaccine exposure during pregnancy week: around conception; second around 5 week and 4 days); Comments: None
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLPFIZER INC2021414258

Write-up: miscarriage, at 9w + 5d she turned out to be pregnant and there appeared to be a non-vital pregnancy; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority, regulatory authority number NL-LRB-00504695. A 31-year-old female patient received bnt162b2, dose 2 via an unspecified route of administration on 25Feb2021 (Batch/Lot Number: EJ6790) as single dose for covid-19 immunisation. Medical history included maternal exposure timing COVID-19 vaccine exposure during pregnancy week: around conception; second around 5 week and 4 days. The patient received BioNTech/Pfizer vaccine on 02Feb2021 for covid-19 immunization. The patient''s concomitant medications were not reported. The patient was diagnosed with missed abortion on 25Feb2021 (other medically important condition), 4 weeks after exposure to covid-19 vaccine Pfizer for covid 19 immunisation. The exposure to this (second) COVID vaccination took place at a pregnancy duration of 5 weeks and 4 days, at that time the patient did not know she was pregnant. The missed abortion (non-vital pregnancy) was diagnosed at a pregnancy duration of 9 weeks and 5 days/ miscarriage, at 9w + 5d she turned out to be pregnant and there appeared to be a non-vital pregnancy. The patient was treated with medication to induce the abortion. The outcome of the event was unknown. No follow-up attempts are possible. No further information is expected. Information about batch number already obtained.; Reporter''s Comments: BioNTech/Pfizer vaccine Past drug therapy BioNTech/Pfizer vaccine: yes ADRs (Adverse drug reaction): miscarriage date: 25Feb2021 Miscarriage Information CIOMS other or disabling information: missed abortion Additional information ADR: relationship with vaccine is unknown; but the patient''s 2nd vaccine was at AD 5 weeks + 4days; on 26Mar she turned out to be pregnant and a non-vital pregnancy confounding factors COVID- 19 vaccine exposure during pregnancy week: around conception; second around AD 5 weeks + 4days COVID19 Previous COVID-19 infection: No Other diagnostic procedures: n/a (not applicable) Reporter note: It could just be that there is no relationship with the vaccination (this cannot be established); I also report at the request of the patient.


VAERS ID: 1058581 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: New York  
Vaccinated:2021-01-14
Onset:2021-02-26
   Days after vaccination:43
Submitted: 0000-00-00
Entered: 2021-02-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3302 / 2 LA / IM

Administered by: Military       Purchased by: ?
Symptoms: Abortion spontaneous, Human chorionic gonadotropin, 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: Prenatal vitamins.
Current Illness: None.
Preexisting Conditions: None.
Allergies: None.
Diagnostic Lab Data: Ultrasound, quantitative HCG measurements.
CDC Split Type:

Write-up: Miscarriage at 6 weeks; 4 days gestation.


VAERS ID: 1097833 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Illinois  
Vaccinated:2021-02-04
Onset:2021-02-26
   Days after vaccination:22
Submitted: 0000-00-00
Entered: 2021-03-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 038K20A / 2 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Human chorionic gonadotropin
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: Metformin Prenatal Vitamins
Current Illness:
Preexisting Conditions:
Allergies: Codeine - migraine
Diagnostic Lab Data: Hcg blood draw on 2/26/2021
CDC Split Type:

Write-up: I had an IUI performed my my OB on 2/1/2021 and received the 2nd dose of the COVID vaccine on 2/4/2021. I found out I was pregnant on 2/15/2021 and found out I was miscarrying on 2/26/2021.


VAERS ID: 1116562 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-01-15
Onset:2021-02-26
   Days after vaccination:42
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012L20A / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Inappropriate schedule of product administration
SMQs:, 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? 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: Patient received first dose of Moderna vaccine on 1/15/21 and was not aware of pregnancy. On 2/12/21, she called and cancelled her 2nd dose appointment because she found out she was pregnant. On 3/16/21 she contacted the pharmacy to schedule a second dose vaccine appointment because she said she had a miscarriage. Called Moderna to report it and Moderna confirmed to give second dose past the 42 days cdc recommendation instead of restarting the series. Patient received 2nd dose on 3/17/21 and has a follow up appointment with OB/GYN on 3/20/21.


VAERS ID: 1130755 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-02-10
Onset:2021-02-26
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-03-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, 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? 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: Ultrasound
CDC Split Type: vsafe

Write-up: On 02-26-2021 I had a miscarriage, I found out my fetus had died during a pre-natal doctor''s appointment. My fetus had expired before I received the first dose Pfizer vaccine. I believe it was coincidental and the Pfizer vaccine did not cause the miscarriage. After my miscarriage I was under heavy medication.


VAERS ID: 1187658 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-14
Onset:2021-02-26
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-04-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Body temperature, Chillblains, Fatigue, Oropharyngeal pain, Pregnancy test positive, Pyrexia, SARS-CoV-2 test negative
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Accidents and injuries (broad), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), 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:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Disease risk factor
Allergies:
Diagnostic Lab Data: Test Date: 20210226; Test Name: koorts 38,9 gr C; Result Unstructured Data: Test Result:38.9 Centigrade; Test Date: 20210227; Test Name: zwangerschapstest: positief; Result Unstructured Data: Test Result: Positive; Test Date: 20210226; Test Name: COVID-19 pcr negatief; Result Unstructured Data: Test Result:Negative
CDC Split Type: NLPFIZER INC2021328315

Write-up: Spontaneous abortion; Chilblains; Throat pain; Pyrexia; Fatigue; This is a spontaneous report from a contactable consumer or other non HCP downloaded from the Medicines Agency. A 31-years-old female patient received BNT162B2 (COMIRNATY), dose 2 via an unspecified route of administration on 14Feb2021 (Batch/Lot Number: Unknown) as single dose for covid-19 immunisation. Medical history included disease risk factor from an unknown date and unknown if ongoing. Historical vaccine included BNT162B2 (COMIRNATY) dose 1 on unspecified date for covid-19 immunisation. The patient''s concomitant medications were not reported. The patient experienced spontaneous abortion (medically significant) (which occurred at an estimated pregnancy duration of "6 weeks, 24 days" [as reported]) on 10Mar2021 after the patient had her second covid-19 vaccination. with outcome of unknown , pyrexia (12 days after start of dose 2) on 26Feb2021 with outcome of recovered , fatigue (12 days after start of dose 2) on 26Feb2021 with outcome of recovered , chilblains (12 days after start of dose 2) on 28Feb2021 described as abnormalities on fingertips and soles of feet of 1-3 mm diameter, purple, very painful to the touch seemed like moisture bumps chilblain-like lesions with outcome of unknown , throat pain (12 days after start of dose 2) on 26Feb2021 with outcome of recovered. The patient underwent lab tests and procedures which included body temperature: 38.9 centigrade on 26Feb2021, pregnancy test positive: positive on 27Feb2021, sars-cov-2 test negative: negative on 26Feb2021. No follow-up attempts possible. No further information expected. Batch/lot cannot be obtained.


VAERS ID: 1304409 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-02-26
Submitted: 0000-00-00
Entered: 2021-05-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed, Abortion spontaneous, Human chorionic gonadotropin, SARS-CoV-2 test, Ultrasound 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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Lactation decreased; Miscarriage; Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Date: 20210127; Test Name: HCG; Test Result: Positive ; Test Date: 20210302; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test; Test Date: 20210226; Test Name: ultrasound; Result Unstructured Data: Test Result:no heartbeat seen
CDC Split Type: GBPFIZER INC2021464270

Write-up: Missed abortion; Miscarriage; This is a spontaneous report from a contactable other HCP. This is a report received from the regulatory authority. Regulatory authority report number is GB-MHRA-WEBCOVID-202104251608290110-XUY8U, Safety Report Unique Identifier: GB-MHRA-ADR 25194440. A 31-year-old female patient received BNT162B2 (COVID-19 MRNA VACCINE BIONTECH, batch/lot number and exp date not reported), dose 1 on an unspecified date, and dose 2 on 05Jan2021; both given via an unspecified route of administration at single dose for COVID-19 immunization. Medical history included miscarriage, pregnancy (1 previous pregnancy. Full term. No complications), and lactation decreased. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Concomitant medication included folic acid (Manufacturer unknown) taken from 01Jan2021 for folic acid supplementation. Patient was exposed to the medicine before pregnancy. Patient''s last menstrual period was on 01Jan2021. Patient tested positive for Human chorionic gonadotropin (HCG) on 27Jan2021. There was no heartbeat seen on ultrasound 26Feb2021. Miscarriage/ Missed abortion was diagnosed (found at 8/40 gestation) on 26Feb2021. Patient required 2 surgical management of miscarriage. Second dose of vaccine was given 5 days before conception. The events were assessed as serious: medically significant and due to hospitalization (date/s unspecified). Patient has not tested positive for COVID-19 since having the vaccine. When asked if the medicine have an adverse effect on any aspect of the pregnancy reply was ''unsure.'' The report does not relate to possible blood clots or low platelet counts. The patient underwent lab tests and procedures which included COVID-19 virus test: No - Negative COVID-19 test on 02Mar2021. The outcome of events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1363352 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-26
Onset:2021-02-26
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

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? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: First pregnancy
Allergies:
Diagnostic Lab Data:
CDC Split Type: IEPFIZER INC2021554128

Write-up: Miscarriage; Maternal exposure during pregnancy, first trimester; This is a spontaneous report from a contactable physician downloaded from the WEB. Regulatory authority report number [IE-HPRA-2021-071220] with Safety Report Unique Identifier [IE-HPRA-2021-071220]. A 37-years-old female patient received bnt162b2 (COMIRNATY), dose 1 via an unspecified route of administration on 26Feb2021 at the age of 37-years-old (Batch/Lot number was not reported) as 1ST DOSE, SINGLE, dose 2 via an unspecified route of administration on 26Mar2021 (Batch/Lot number was not reported) as 2ND DOSE, SINGLE for covid-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient experienced maternal exposure during pregnancy, first trimester on 26Feb2021, miscarriage on 03Apr2021. It was reported on 03Apr2021, 8 days post-vaccination, the patient experienced a miscarriage at 8 weeks pregnant. The events were reported as serious due to medically significant. The mother reported she became pregnant while taking bnt162b2. It was noted that was the patient''s first pregnancy. At the time of reporting, the patient had recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1094454 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-02-11
Onset:2021-02-27
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-03-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 030M20A / 1 LA / SYR

Administered by: School       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Back pain, Blood test, Exposure during pregnancy, Ultrasound antenatal screen abnormal
SMQs:, Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic 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? 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: prenatal vitamins with choline tablet (One-A-Day) Calcium supplement with Vitamin D
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: I had my blood drawn, an ultrasound, and a pelvic exam in the Emergency Room on 2/27/2021. Results were consistent with incomplete miscarriage at that time. No other abnormalities were noted.
CDC Split Type:

Write-up: I experienced a miscarriage on February 27th, 2021. I was approximately 10 weeks pregnant when I experienced the miscarriage. It was accompanied by severe pain/cramps in the abdomen and lower back. Expected delivery would have been in September 2021. This was my first pregnancy.


VAERS ID: 1370198 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-30
Onset:2021-02-27
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-06-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6797 / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Antiphospholipid antibodies, Antiphospholipid antibodies positive, Blood grouping
SMQs:, Systemic lupus erythematosus (broad), 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? 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: Test Date: 202103; Test Name: Antiphospholipid antibodies; Test Result: Positive ; Test Name: Blood typing; Result Unstructured Data: Test Result:B+
CDC Split Type: PTPFIZER INC2021559337

Write-up: the antiphospholipid antibodies were tested with a positive result; Spontaneous abortion at 6 weeks of pregnancy, 4 weeks after the 2nd dose of Comirnaty; This is a spontaneous report from a contactable pharmacist downloaded from the regulatory authority-WEB. The regulatory authority is PT-INFARMED-T202104-1415. A 32-year-old female patient received second dose of BNT162B2 (COMIRNATY), via intramuscular on 30Jan2021 (Lot Number: EJ6797, at the age of 32-year-old) as 0.3 ml, single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient previously took first dose of BNT162B2 (COMIRNATY), via intramuscular on 09Jan2021 as single dose for covid-19 immunisation. On 27Feb2021, patient experienced spontaneous abortion at 6 weeks of pregnancy, 4 weeks after the 2nd dose of Comirnaty. Pregnant B+ on unspecified date, without history of previous miscarriages. She had 4 pregnancies with 4 births. No information was available on known diseases or a history of infection COVID-19. The adverse reaction (ADR) happened 4 weeks after the administration of the 2nd dose of the suspect medication, without the need for specific treatment. In the month following the ADR (Mar2021), the antiphospholipid antibodies were tested with a positive result. According to the opinion of the notifier, the causal link to the reported ADR was possible. There was no suspicion of interaction between medications or medication errors. The outcome of the events "Spontaneous abortion at 6 weeks of pregnancy, 4 weeks after the 2nd dose of Comirnaty" was recovered on 27Feb2021, the outcome of event "the antiphospholipid antibodies were tested with a positive result" was unknown. Reporter''s comments: Concomitant Medication-Unknown. Did a Medication Error occur?-No. Other information-She took the first vaccine in early Jan2021, 2nd in late Jan2021, becomes pregnant (B +) in mid-January and has a miscarriage in late Feb2021. No history of previous abortions and 4 pregnancies with 4 births. Antiphospholipid + antibody analyzes, in mid-March. Relatedness of drug to reaction(s)/event(s) for event Abortion spontaneous: Source of assessment: Notifier; Method of assessment: Unknown; Result of Assessment: Possible. No follow-up attempts are needed. No further information is expected.; Reporter''s Comments: Concomitant Medication-Unknown. Did a Medication Error occur?-No. Other information-She took the first vaccine in early Jan2021, 2nd in late Jan2021, becomes pregnant (B +) in mid-January and has a miscarriage in late Feb2021. No history of previous abortions and 4 pregnancies with 4 births. Antiphospholipid + antibody analyzes, in mid-March.


VAERS ID: 1064123 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Kentucky  
Vaccinated:2021-02-16
Onset:2021-02-28
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-03-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9269 / 2 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal death, 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? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Lantus Valtrex Phenergan Cyclobenzaprine Prenatal Vitamin Unisom
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: Ultrasound in hospital 2/28/2021 D&E scheduled 3/2/2021
CDC Split Type:

Write-up: Fetal demise sometime between 15-18 weeks based on ultrasound findings. EDC 7/30/2021


VAERS ID: 1119455 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-14
Onset:2021-02-28
   Days after vaccination:45
Submitted: 0000-00-00
Entered: 2021-03-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH NOT KNOWN / 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? 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: FOLIC ACID; PARACETAMOL
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Fever; Lactation decreased; Suspected COVID-19
Allergies:
Diagnostic Lab Data: Test Date: 20200616; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:Yes - Positive COVID-19 test
CDC Split Type: GBPFIZER INC2021244524

Write-up: 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-202103040924324980, Safety Report Unique Identifier GB-MHRA-ADR 24873244. A 35-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date were not reported) via an unspecified route of administration on 14Jan2021 as a single dose for COVID-19 immunization. Medical history included lactation decreased, suspected covid-19 from 14Jun2020 to 21Jun2020 and fever. Patient was not enrolled in clinical trial. Patient was not currently breastfeeding. Patient no longer pregnant at the time of reporting. Concomitant medication included folic acid taken for Folic acid supplementation and paracetamol (PARACETAMOL) taken for Fever start from 14Jan2021 to 16Jan2021. The patient had early miscarriage (reported as medically significant, congenital anomaly) on 28Feb2021 with outcome of recovering. The mother reported she became pregnant while taking bnt162b2. The patient underwent lab tests and procedures which included yes - positive covid-19 test on 16Jun2020. 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 first-trimester (1-12 weeks). Details of scans or investigations: Heartbeat seen at 6 weeks, no longer there at 7+4. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1162344 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-27
Onset:2021-02-28
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-04-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP9598 / 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: PAROXETINE
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Maternal vaccine exposure (COVID-19 vaccine exposure during pregnancy week: I was not pregnant yet)
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLPFIZER INC2021302442

Write-up: Whether it is related is still very much a question, but I had a miscarriage.; This is a spontaneous report from a contactable consumer or other non hcp downloaded from an Agency- WEB received via Regulatory Authority, with regulatory authority report number NL-LRB-00474309. A pregnant adult female patient received the second dose of bnt162b2 (COMIRNATY), via an unspecified route of administration on 27Feb2021 (Lot Number: EP9598) at 0.3 ml single for COVID-19 immunisation. Medical history included maternal vaccine exposure: COVID-19 vaccine exposure during pregnancy week: patient was not pregnant yet (information presented as reported). The patient did not have previous COVID-19 infection. Concomitant medications included paroxetine (10mg tablet) from an unknown date at an unknown dose for an unspecified indication. The patient previously received the first dose of bnt162b2 (COMIRNATY, Lot number unknown), via an unspecified route of administration on 04Feb2021 for COVID-19 immunisation, the patient stated at the first dose of the vaccine she was not pregnant yet, but at the second vaccination she knew that she was early pregnant. Because of working in healthcare the patient decided to get the vaccination. The patient experienced a miscarriage on 28Feb2021. The patient stated that whether it is related is still very much a question. The miscarriage occurred at gestational age 4 weeks and 3 days, one day after the second COVID-19 vaccination. The pregnancy resulted in spontaneous abortion. The outcome of the event was unknown. Sender Comment: Since the nature of the reported reaction does imply seriousness according to one of the agency criteria, the reaction was considered as serious by an agency. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : NL-PFIZER INC-2021357085 1st/2nd dose of the vaccine, same patient


VAERS ID: 1377234 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-18
Onset:2021-02-28
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-06-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1404 / 2 LA / -

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? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210310; Test Name: rapid test; Test Result: Negative
CDC Split Type: CAPFIZER INC2021619415

Write-up: miscarriage 9 days after the 2nd shot; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) dose 2 via an unspecified route of administration, administered in arm left on 18Feb2021 14:45 (Lot Number: EL1404) as 2nd dose, single dose, dose 1 via an unspecified route of administration, administered in arm left on 14Jan2021 (Batch/Lot Number: unknown) as 1st dose, single dose for covid-19 immunisation. Known allergies included tobradex eye drops, canesten. No other medical history. Facility type vaccine was nursing home/senior living facility. No other vaccine in four weeks. No other medications in two weeks. No covid prior vaccination. The patient was pregnancy at time of vaccination. The Last menstrual date was 03Jan2021. Gestation period when reaction/event was observed in the fetus was reported as 3 weeks. The patient had miscarriage 9 days after the 2nd shot on 28Feb2021 14:00. No Hospitalization Prolonged. The event resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. The patient had covid tested (Rapid Test, Nasal Swab) post vaccination on 10Mar2021 with negative result. Treatment was received for event. The outcome of event was not recovered.


VAERS ID: 1101580 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-01-27
Onset:2021-03-01
   Days after vaccination:33
Submitted: 0000-00-00
Entered: 2021-03-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EZ23248 / 2 RA / IM

Administered by: Senior Living       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: Zyrtec
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: vsafe

Write-up: I received my second dose Pfizer vaccine 01-27-2021. I found out I was pregnant the beginning of March 2021. On 03-10-2021, I found out I was having a miscarriage. I am in the process of recovering.


VAERS ID: 1103353 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Illinois  
Vaccinated:2021-02-15
Onset:2021-03-01
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-03-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 024M20A / 1 LA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 006B21A / 2 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Exposure during pregnancy, Transfusion, Ultrasound uterus, 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? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Pre-Natal Vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: Augmentin, Vancomycin
Diagnostic Lab Data: Ultra Sound, Blood work on 3/1/21 (No fetal heart tones) Ultra Sound confirming no heart beat 3/8/21 Blood Transfusions on 3/5/21 Dilation and Curettage on 3/8/21
CDC Split Type:

Write-up: Miscarriage 2 weeks after receiving the first dose (March 1, 2021). Baby had a heart beat, then slowly died. Ultra Sound Showing Fetal Bradycardia on 2/26/21.


VAERS ID: 1135569 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-02-19
Onset:2021-03-01
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-03-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9269 / 1 RA / -

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? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Rheumatoid arthritis
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021289435

Write-up: Early miscarriage; This is a spontaneous report from a contactable other health care professional (Patient). A 30-year-old female patient (pregnant, last menstrual date 19Jan2021, Delivery date: 26Oct2021, Gestational period 4 weeks) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL9269), via an unspecified route of administration on right arm on 19Feb2021 at 15:15 at the age of 30 years old at a single dose for COVID-19 immunisation at hospital. The patient''s medical history included rheumatoid arthritis. There were no known allergies. Concomitant medications included prenatal vitamin. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received other medications within 2 weeks of vaccination. The patient experienced early miscarriage on 01Mar2021. No treatment was received in response to the adverse event. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, patient was not tested for COVID-19. The patient was recovering from the event. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Pending the limited information on clinical course, the company does not attribute the event early miscarriage to BNT162B2. The detailed document of pregnancy, relevant risk factors, status of rheumatoid arthritis 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: 1163458 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Virginia  
Vaccinated:2020-12-01
Onset:2021-03-01
   Days after vaccination:90
Submitted: 0000-00-00
Entered: 2021-04-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA MODERNA / 1 - / SYR
UNK: VACCINE NOT SPECIFIED (NO BRAND NAME) / UNKNOWN MANUFACTURER MODERNA / 2 LA / SYR

Administered by: Public       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? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: 2 prior first trimester miscarriages unrelated. 1 second trimester miscarriage at 21weeks gestation in March 2021, normal weight and size at time of delivery. Vaccine was given 12/2020 and 1/2021


VAERS ID: 1228794 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-03-16
Onset:2021-03-01
Submitted: 0000-00-00
Entered: 2021-04-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test abnormal, Exposure during pregnancy, Human chorionic gonadotropin decreased, 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), Fertility disorders (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: Euthyrox, Sertraline, aspirin, folic acid, prenatal,
Current Illness:
Preexisting Conditions: Hypothyroidism, Anxiety/Depression, Obesity
Allergies:
Diagnostic Lab Data: HCG levels drawn 4/15 and 4/17
CDC Split Type:

Write-up: Was unknowingly pregnant at the time of first and second shot. Found out I was pregnant and miscarrying the day of the second shot (4/6/21). Don?t know if the vaccine caused the miscarriage but I thought i should report it. Started bleeding within hours of the second shot and blood tests on 4/15 and 4/17 showed I was losing the pregnancy.


VAERS ID: 1232831 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Illinois  
Vaccinated:2021-01-08
Onset:2021-03-01
   Days after vaccination:52
Submitted: 0000-00-00
Entered: 2021-04-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1283 / 2 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Antiphospholipid antibodies positive, Exposure during pregnancy, Laboratory test normal, SARS-CoV-2 test negative
SMQs:, Systemic lupus erythematosus (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), 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 vitamin
Current Illness: no
Preexisting Conditions: no
Allergies: no
Diagnostic Lab Data: D@E done on March 12; (out patient surgery) - at Hospital - COVID test - negative; sent to pathology and genetic testing - all was normal; Prenatal genetic testing (I had) which was normal either. At Doctor''s office - On April 2nd - had blood work done - for testing for lupus anti coagulants and that came back positive.
CDC Split Type: vsafe

Write-up: I had a missed miscarriage at my 15 week check up. Baby had passed away in the weeks prior. I found out about March 10. Pregnancy history - 2nd one - 2016 - normal pregnancy; this was my second pregnancy; due date was August 19th. I do have to have repeat testing in three months to confirm lupus anti-coagulants result from April 2nd.


VAERS ID: 1279405 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2021-03-26
Onset:2021-03-01
Submitted: 0000-00-00
Entered: 2021-05-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8730 / 1 LA / -

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

Life Threatening? Yes
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: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Allergies:
Diagnostic Lab Data: Test Date: 20210422; Test Name: COVID-19 test; Test Result: Negative ; Comments: nasal swab
CDC Split Type: USPFIZER INC2021456214

Write-up: miscarriage of the 16-17 week fetus; This is a spontaneous report from a contactable consumer (patient). A 30-year-old female patient received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number : ER8730), via an unspecified route of administration, administered in the left arm on 26Mar2021 at 16:30 as a single dose for COVID-19 immunization. The patient had no medical history and no known allergies. The patient''s concomitant medications included unspecified prenatal vitamins. The patient did not have other vaccines in four weeks prior to the COVID vaccine. On an unspecified date in Mar2021, the patient had a miscarriage of the 16-17 week fetus. The patient had surgery to remove the fetus and tissue. The mother was due to deliver on 09Sep2021. The outcome of the event was recovering. The patient had a nasal swab COVID-19 test on 22Apr2021 with a result of negative. The event was reported as life-threatening.


VAERS ID: 1301074 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-03-17
Onset:2021-03-01
Submitted: 0000-00-00
Entered: 2021-05-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Biochemical pregnancy
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: Prenatal vitamin
Current Illness: None
Preexisting Conditions: Celiac disease
Allergies: Gluten (celiac disease)
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage (chemical pregnancy). I didn?t test positive for pregnancy until a week after my vaccine so I put ?unknown? for pregnant at the time of vaccine. I then tested negative a couple days later and had the miscarriage 2 weeks and 2 days after my vaccine


VAERS ID: 1301673 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-01
Onset:2021-03-01
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-05-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029L20A / 2 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Abortion induced, Amniocentesis, Exposure during pregnancy, Gene mutation identification test, 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? 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: Prenatal
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data: Genetic tests Ultrasounds Amniocentesis
CDC Split Type:

Write-up: I was 14 weeks pregnant for shot 1 and 18 weeks pregnant for shot 2. My 12 week anatomy scan showed my baby was healthy, all NIPT and amnio came back clean. My baby developed Microcephaly by the next ultrasound scan, 19 weeks. Between 19-23 weeks, her brain slowed down in development even further. I terminated the pregnancy


VAERS ID: 1529171 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Kansas  
Vaccinated:2021-01-08
Onset:2021-03-01
   Days after vaccination:52
Submitted: 0000-00-00
Entered: 2021-08-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3248 AND EL92 / 2 AR / IM

Administered by: Work       Purchased by: ?
Symptoms: Abortion induced, Amniocentesis abnormal, Artificial insemination, Chromosome analysis abnormal, Foetal chromosome abnormality, Maternal exposure before pregnancy
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), Fertility disorders (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: Swelling and redness in arm one time after a flu vaccine, several years ago.
Other Medications: Azalaic acid gel 15%, Clindamycin Phosphate 1.0% lotion, Omeprazole DR, Fluticasone, Tylenol extra strength, Melatonin, prenatal multi-vitamin, and Cetirizine.
Current Illness: None
Preexisting Conditions: Hepatic adenomatosis.
Allergies: Iodine-containing contrast dye.
Diagnostic Lab Data: Amniocentesis and microarray.
CDC Split Type:

Write-up: I received the Pfizer COVID-19 vaccine through my employer. My first dose was 1/8/21 and my second dose was 1/29/21. I became pregnant through a subsequent IUI cycle on 3/19/2021. We had an amniocentesis at 16 weeks and the results indicated that the baby had a rare chromosomal abnormality - a 1q21.1 microdeletion. I don''t think this is related to the vaccine but I wanted to report it. My husband and I are awaiting our own genetic test results to see if we passed it on to the baby or if it was de novo. We ultimately decided to terminate the pregnancy that we wanted so badly due to the high risk for physical and cognitive impairments for our baby. We are devastated.


VAERS ID: 1583162 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Nevada  
Vaccinated:2021-02-08
Onset:2021-03-01
   Days after vaccination:21
Submitted: 0000-00-00
Entered: 2021-08-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012M20A / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood glucose normal, Blood potassium decreased, Differential white blood cell count, Full blood count, Glomerular filtration rate, Haematocrit decreased, Haemorrhage, Haemorrhage urinary tract, Lipase, Metabolic function test, Muscle spasms, Red blood cell count decreased, Red blood cells urine, Sexually transmitted disease, Ultrasound pelvis, Urine analysis, Vaginal haemorrhage
SMQs:, Haematopoietic erythropenia (narrow), Haemorrhage terms (excl laboratory terms) (narrow), Haemorrhage laboratory terms (broad), Dystonia (broad), Termination of pregnancy and risk of abortion (narrow), Hypokalaemia (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: Multivitamins, Kesimpta, no changes.
Current Illness: None
Preexisting Conditions: Multiple Sclerosis
Allergies: All -cillins (suspected due to clinical reaction), shrimp, latex
Diagnostic Lab Data: 3/2/2021, at Emergency Department: pregnancy tests negative. CBC with differential, comp metabolic panel, urinalysis, lipase, estimated GFR, STI screenings, pelvic ultrasound, urine microscopic, wet prep. Results normal except: RBC 3.67 (low), Hematocrit 35.2 (low), Potassium 3.4 (low), Glucose 100 (high), RBC in urine 20-50.
CDC Split Type:

Write-up: Abnormal vaginal bleeding and severe cramping, began on 3/1/2021, outside of overall regular and predictable cycle. Approximately 1 tennis ball size amount of blood clots and light bleeding after. 4x severe cramps, like labor contractions, just prior to passing blood clots. Suspected possible miscarriage in not yet detected pregnancy. Family member and on call medical assistant for patient''s PCP encouraged ER visit on 3/2/2021. First vaccine administration was done on 1/11/2021 Moderna Lot number 011L20A.


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