National Vaccine
Information Center

Your Health. Your Family. Your Choice.

MedAlerts Home
Search Results

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)

This is page 4 out of 27

Result pages: prev   1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27   next


VAERS ID: 990450 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Indiana  
Vaccinated:2021-01-11
Onset:2021-01-16
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-02-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ES1686 / 2 LA / OT

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

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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210111; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20210113; Test Name: Nasal Swab; Test Result: Negative
CDC Split Type: USPFIZER INC2021035452

Write-up: Miscarriage after 2nd vaccine.; Miscarriage after 2nd vaccine.; Miscarriage after 2nd vaccine.; Miscarriage after 2nd vaccine.; This is a spontaneous report from a contactable nurse reported for herself. This 33-year-old female patient received the 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: Es1686), via intramuscular at left arm on 11Jan2021 08:00 am at single dose for COVID-19 immunisation. Medical history was unknown. Concomitant medications were none. The patient previously received the 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: Ej1685) intramuscular at left arm on 21Dec2020 10:15 AM for COVID-19 immunisation. The patient had no known allergies. The patient had no other vaccine in four weeks, no other medications in two weeks. The patient was pregnant. Last menstrual date was 14Dec2020. Delivery due date was 16Sep2021. Gestation period was 3 weeks. The patient experienced miscarriage on 16Jan2021 after 2nd vaccine. AE resulted in congenital anomaly or birth defect. The patient had no COVID prior vaccination. The patient had COVID tested/nasal swab post vaccination with negative results on 11Jan2021 and 13Jan2021. Outcome of the events was unknown.; Sender''s Comments: Based on the available information, a causal relationship between event miscarriage after the second COVID-19 vaccination and BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) cannot be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.


VAERS ID: 1006011 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-01-16
Onset:2021-01-16
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-02-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3248 / 1 LA / -

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? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Asthma; COVID-19
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021063959

Write-up: Miscarriage; The mother reported she became pregnant while taking bnt162b2; The mother reported she became pregnant while taking bnt162b2; This is a spontaneous report from a contactable consumer reported for herself. A 27-year-old female patient (Pregnant) received first dose of bnt162b2 (lot number: EL3248), via an unspecified route of administration in left arm on 16Jan2021 16:30 at single dose for covid-19 immunization. Medical history included asthma, covid-19 from an unknown date and unknown if ongoing. The patient''s concomitant drug included prenatal vitamins. The patient experienced miscarriage on 21Jan2021 with outcome of recovering. The event was reported as non-serious. The adverse event result in emergency room/department or urgent care. No treatment received for the adverse event. 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 19Aug2021. Last menstrual date: 22Nov2020. Facility where the most recent COVID-19 vaccine was administered: Hospital. The patient was not received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient hadn''t been tested for COVID-19. Not known allergies to medications, food, or other products.


VAERS ID: 1042278 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-09
Onset:2021-01-16
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-02-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1484 SC 04/21 / 1 LA / OT

Administered by: Other       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? 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: ITPFIZER INC2021126190

Write-up: AFTER THE ADMINISTRATION OF THE FIRST DOSE: SUSPECTED ABORTION AT 6 WEEKS OF PREGNANCY.; This is a spontaneous report from a contactable physician downloaded from the WEB IT-MINISAL02-666260, received from Regulatory Authority. A 40-years-old female patient received first dose bnt162b2 (COMIRNATY, solution for injection, lot number: EL1484 SC 04/21, expiry date not reported), intramuscular on 09Jan2021 18:51 at 30 ug, single in the left deltoid for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient under the vaccine administration was not aware of being pregnant. On 16Jan2021, the patient experienced suspected abortion at 6 weeks of pregnancy after the administration of the first dose. The reaction happened 7 days after the administration of the vaccine. The event was reported as serious medically significant event. The outcome of the event suspected abortion was reported as recovered/resolved with sequel. No follow-up attempts possible. No further information expected.


VAERS ID: 985511 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-04
Onset:2021-01-17
   Days after vaccination:13
Submitted: 0000-00-00
Entered: 2021-01-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 RA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: VITAMIN C PRENATAL
Current Illness: NO OTHER ILLNESSES
Preexisting Conditions: NO OTHER HEALTH CONDITIONS
Allergies: NO ALLERGIES
Diagnostic Lab Data: HCG NEGATIVE PREGNANCY HOME TEST NEGATIVE AFTER
CDC Split Type:

Write-up: 1/4 - RECEIVED MODERNA VACCINE, PREGNANCY TEST CAME OUT NEGATIVE. 1/8 - PREGNANCY TEST CAME OUT POSITIVE 1/18 - HAD MISCARRIAGE, SAW TISSUE, NEGATIVE PREGNANCY HOME TEST, NEGATIVE HCT


VAERS ID: 1006634 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-06
Onset:2021-01-17
   Days after vaccination:11
Submitted: 0000-00-00
Entered: 2021-02-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 037K20A / 1 AR / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamin
Current Illness: none
Preexisting Conditions: asthma, migraine
Allergies: Ceclor, doxycycline, PCN, sulfa
Diagnostic Lab Data: 1/19/21 - ultrasound confirming embryonic demise 1/20/21 - D&C for incomplete abortion
CDC Split Type:

Write-up: Spontaneous abortion. Pt was 9w1d at time of first Moderna COVID vaccine (EDD 8/9/2021). Two weeks later she began bleeding and was found to have an incomplete abortion with embryo measuring 9w1d. Proceeded to bleed heavily and D&C performed. Uncomplicated recovery. Genetic studies in process. Unknown if SAB is related to vaccine, though it appears embryonic demise occurred within a few days of vaccine administration.


VAERS ID: 1076637 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-14
Onset:2021-01-17
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-03-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 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? 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: ROPFIZER INC2021221018

Write-up: Spontaneous abortion; This is a spontaneous report downloaded from the Regulatory Authority-WEB with regulatory authority number (RO-NMA-2021-SP40060) and Sender''s (Case) Safety Report Unique Identifier (RO-NMA-2021-SP40060). A contactable consumer (patient) reported that an adult female patient received first dose of BNT162B2 (COMIRNATY), on 14Jan2021 at single dose for covid-19 immunization. The patient medical history and the concomitant medications were not reported. The patient experienced spontaneous abortion on 17Jan2021. The outcome was unknown. The mother reported she became pregnant while taking bnt162b2. The pregnancy resulted in spontaneous abortion. No follow-up attempts are possible, information about batch/lot number cannot be obtained.


VAERS ID: 958755 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-12
Onset:2021-01-18
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-01-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK9231 4/21 / 1 - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal death, Premature delivery, Premature separation of placenta, Stillbirth, Ultrasound antenatal screen normal, 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), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: prenatal vitamins
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt was 18 weeks pregnant at the time of the vaccine. Second pregnancy. Pt is a physician. Pregnancy was entirely normal up to that time. On 1/18/2021, she began to have heavy vaginal bleeding probably due to a placental abruption and subsequently delivered at 18 weeks. Baby was stillborn. Ultrasound done 1/15/2021 normal. Lethal event for the fetus. The patient did well.


VAERS ID: 970929 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Florida  
Vaccinated:2020-12-30
Onset:2021-01-18
   Days after vaccination:19
Submitted: 0000-00-00
Entered: 2021-01-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 039K20A / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound foetal abnormal
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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins, iron, calcium
Current Illness: No
Preexisting Conditions: None
Allergies: NKDA
Diagnostic Lab Data: Ultrasounds were completed on facility. On 1/17, after sx of bleeding a low fetal heartbeat was found. On the 20th, it was found that there was no heartbeat.
CDC Split Type:

Write-up: A miscarriage was determined on 1/18/2021. There is no history of miscarriages.


VAERS ID: 1006169 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-01-14
Onset:2021-01-18
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-02-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, COVID-19, Exposure during pregnancy, Full blood count, Haemorrhage, Human chorionic gonadotropin positive, Pregnancy, Pregnancy test positive, Surgery, Transfusion, Ultrasound abdomen abnormal, Ultrasound scan vagina
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Tumour markers (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Celexa, 40mg daily, Naltrexone, 50 mg daily, Cranberry supplement x1 Daily
Current Illness: Yes diagnosed as COVID positive on 12/24/20
Preexisting Conditions: no
Allergies: Sulfa, morphine
Diagnostic Lab Data: OTC pregnancy test 1/20/21 Beta HCG 1/20/21 CBC and follow-up CBC 1/20/21 and 1/21/21 Vaginal and abdominal Ultrasounds 1/20/21
CDC Split Type:

Write-up: I was approximately 4 weeks pregnant at the time that I received dose #1 (12/23/20)- I was unaware of the pregnancy. I was diagnosed with COVID on 12/28/20, but was first symptomatic on 12/24. I attributed my s/s initially to the vaccine. I was eventually tested on 12/28/20, as my symptoms worsened and I was positive for COVID. On 1/14/21 I received my second dose, my COVID s/s had been resolved since 1/4/21. On the evening of 1/18/21 I started experiencing mild abdominal pain. This progressed, on the evening 1/20 the pain was no longer tolerable. I went to the ER where I hemorrhaged and needed emergency surgery and a blood transfusion for a miscarriage. The surgery ultimately took place in the early morning hours of 1/22/21, followed by the blood transfusion.


VAERS ID: 1030825 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-01-15
Onset:2021-01-18
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-02-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: COVID-19, Diarrhoea, Headache, Oropharyngeal pain, Premature delivery, Premature labour, Respiratory tract congestion, SARS-CoV-2 test positive
SMQs:, Pseudomembranous colitis (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Noninfectious diarrhoea (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (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 Vit
Current Illness: No
Preexisting Conditions: No
Allergies: Codeine
Diagnostic Lab Data: Covid test 1/18(results positive)
CDC Split Type: vsafe

Write-up: I had a headache, diarrhea, sore throat and congestion. The congestion lasted for about a week .My water broke on 1/20/2021 and gave birth on 1/21/2021 I was 34 1/2 weeks. It depends on how you look at it I think Covid caused the premature labor.


VAERS ID: 993407 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2020-12-07
Onset:2021-01-18
   Days after vaccination:42
Submitted: 0000-00-00
Entered: 2021-02-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH NOT KNOWN / UNK - / -

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? 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
Current Illness: Pregnancy
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage (previous pregnancies: P2+2 - 2 early miscarriages prior)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result: No - Negative COVID-19 test; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result: has not tested positive for COVID-19; Comments: since having the vaccine; Test Name: scans; Result Unstructured Data: Test Result: likely failing pregnancy
CDC Split Type: GBPFIZER INC2021053198

Write-up: Early miscarriage; This is a spontaneous report from a contactable physician. This is a report received from the Regulatory authority. Regulatory authority report number GB-MHRA-WEBCOVID-202101191033464870, Safety Report Unique Identifier GB-MHRA-ADR 24613660. A 40-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; batch/lot number and expiration date unknown), via an unspecified route of administration on 07Dec2020 at a single dose for COVID-19 immunization. Medical history included ongoing pregnancy and 2 early miscarriages prior (previous pregnancies: P2+2). The patient was otherwise fit and well. Patient has not had symptoms associated with COVID-19 and is not enrolled in clinical trial. Concomitant medication included folic acid as folic acid supplementation. The patient experienced an early miscarriage on 18Jan2021. The event was assessed as serious due to congenital anomaly. The patient was 8 weeks pregnant at the onset of the event. The patient''s last menstrual period date was on 23Nov2020. The patient had previous pregnancies reported as "P2+2" with 2 early miscarriages prior to this. The patient was exposed to the medicine during the first trimester (1-12 weeks). Scan at 8 weeks showed likely failing pregnancy. Patient has not tested positive for COVID-19 since having the vaccine. The patient underwent lab tests and procedures which included COVID-19 virus test: no - negative covid-19 test on an unspecified date. The outcome of the event was not recovered. No follow-up attempts are possible, information about batch/lot number cannot be obtained.


VAERS ID: 1132563 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-18
Onset:2021-01-18
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-03-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0739 / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ELOINE; FOLIC ACID; MONTELUKAST; SYMBICORT
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Asthma (Shielding with severe asthma)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021262773

Write-up: Maternal exposure during pregnancy; Pain; Fatigue; Miscarriage; This is a spontaneous report from a contactable other healthcare professional (HCP) received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-APPCOVID-202103090954015660, Safety Report Unique Identifier GB-MHRA-ADR 24904117. A 29-year-old female patient received the first dose (dose 1) of BNT162B2 (PFIZER-BIONTECH, COVID-19 MRNA VACCINE, lot Number: EL0739) via an unspecified route of administration on 18Jan2021 at a single dose for COVID-19 immunisation. Medical history included shielding with severe asthma. Concomitant medications included drospirenone/ethinylestradiol betadex clathrate (ELOINE) from 01Sep2019 to 01Nov2020 for contraception; folic acid from an unspecified date as folic acid supplementation; montelukast from 01Nov2019 for asthma; and budesonide/formoterol fumarate (SYMBICORT) from 01Apr2020 for asthma. The patient had maternal exposure during pregnancy on 18Jan2021 and experienced pain and fatigue on 18Jan2021. The patient was noted to have a miscarriage on 2021. This was the patient''s first pregnancy and was exposed to the medicine first-trimester (1-12 weeks). This case was assessed as serious medically significant. The patient was not currently breastfeeding. She was no longer pregnant at the time of reporting. The patient has not had symptoms associated with COVID-19, has not tested positive for COVID-19 since having the vaccine, and was not enrolled in clinical trial. The patient underwent lab tests which included COVID-19 virus test: negative (no - negative COVID-19 test) on an unspecified date. The outcome of the events fatigue and pain was recovered on 20Jan2021 and 21Jan2021 respectively. The outcome of the event miscarriage was recovering. It was not sure if the vaccine had any adverse effect on any aspect of pregnancy. No follow-up attempts are possible. No further information is expected.


VAERS ID: 964070 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Rhode Island  
Vaccinated:2021-01-17
Onset:2021-01-19
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-01-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3302 / 2 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Heavy menstrual bleeding, Pregnancy
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

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

Write-up: Hi, I actually not sure if the couse of my problem was couse by the Vaccine given to me on January 17 2021. At the time of the injection given to me I was pregnant don''t know how long because I just had found out about it. I took the injection because I wanted to be safe for the health of my baby and my family..am just curious about the side effect of this covi19 vaccine. On January 19 I started seen some spot of blood at first I thought it was nothing to worried about but then around 8am I that day I saw that I was bleeding more and more not a crazy bleeding but I ended up at the emergency room on January 19 around 3:45pm. To find out that I was having a miscarriage..so now I don''t know if this was couse by the injection or not. Am just worried that these is a side effect of this injection and nobody knows about it. Please reply me back I want to know more I already have both covi19 vaccine.


VAERS ID: 1259263 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-19
Onset:2021-01-19
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL8982 / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Anembryonic gestation, Fatigue, Muscle spasms, Pain in extremity, Ultrasound antenatal screen
SMQs:, Dystonia (broad), 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? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 1st dose Pfizer - sore arm; fatigue starting the evening of the vaccine- for 24 hours 12/28/2021
Other Medications: prenatal vitamins
Current Illness: no
Preexisting Conditions: no
Allergies: no
Diagnostic Lab Data: Ultrasound - 4/14/2021 -
CDC Split Type: vsafe

Write-up: Sore arm and fatigue that first evening. I had those for about 24 hours. Miscarriage - I had my first doctor''s appt on 4/14/2021 and I found out that there was no embryo - Anembryonic pregnancy (blighted ovum)- my body thought it was pregnant but there was no embryo. I had to take medication to induce the miscarriage - I took that last week on the 20th. I''ve passed all the tissue but I have to wait for it stop cramping now.


VAERS ID: 1076292 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-19
Onset:2021-01-19
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-03-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Pain, Paraesthesia, SARS-CoV-2 test
SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), 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:
Allergies:
Diagnostic Lab Data: Test Date: 20201202; Test Name: COVID-19 virus test; Test Result: Negative
CDC Split Type: GBPFIZER INC2021186450

Write-up: Miscarriage / Patient was exposed to the medicine first-trimester (1-12 weeks); Pain; Pins and needles; This is a spontaneous report from a contactable consumer from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202102181308032530, Safety Report Unique Identifier GB-MHRA-ADR 24788363. A 37-year-old female patient (pregnant at the time of vaccination) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: unknown and expiry date was unknown), via an unspecified route of administration on 19Jan2021 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Patient no longer pregnant at the time of reporting. Patient has not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. The patient underwent lab tests and procedures which included COVID-19 virus test and resulted as negative on 02Dec2020. Patient was exposed to the medicine first-trimester (1-12 weeks). Patient did not take folic acid supplement during pregnancy. Patient has not tested positive for COVID-19 since having the vaccine. The patient experienced pins and needles on 19Jan2021, had pain on 21Jan2021 and had miscarriage on 03Feb2021. This case was reported as serious with seriousness criteria other medically important condition from HA. The outcome of the event Pins and needles was recovered on 20Jan2021, Pain was recovered on 22Jan2021, Miscarriage was recovered on 14Feb2021 and for Patient was exposed to the medicine first-trimester (1-12 weeks) it was unknown. No follow-up attempts are possible, information about batch/lot number cannot be obtained.


VAERS ID: 1244119 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-19
Onset:2021-01-19
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK4237 / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: L-THYROXINE [LEVOTHYROXINE]
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Hyperthyroidism; Pregnancy; Thyroidectomy
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021382353

Write-up: neck ache; chills; Early miscarriage; Maternal exposure during pregnancy; This is a spontaneous report from a contactable physician received from the Regulatory Agency (RA). Regulatory authority report number is GB-MHRA-WEBCOVID-202104061312239940, Safety Report Unique Identifier is GB-MHRA-ADR 25086372. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 19Jan2021 (Lot Number: EK4237, expiry date not reported) as single dose for COVID-19 immunization. Medical history included hyperthyroidism from 2015 to an unknown date, thyroidectomy from an unknown date and unknown if ongoing, and pregnancy from an unknown date and unknown if ongoing. Patient had not had symptoms associated with COVID-19. Patient had not had a COVID-19 test. Patient was not enrolled in clinical trial. Patient had not tested positive for COVID-19 since having the vaccine. Concomitant medication included l-thyroxine taken for post procedural hypothyroidism from 11Mar2015 to an unspecified stop date. The patient experienced early miscarriage on 04Mar2021 with outcome of recovered on 05Mar2021, neck ache on an unspecified date with outcome of unknown, and chills on an unspecified date with outcome of unknown. The events were reported as serious, disability. Narrative case summary and further information: Was unknowingly 2/40 pregnant (first pregnancy) when had first dose of Pfizer vaccine. Side effects for one night of chills and neck ache. Miscarried at 11/40. No follow up attempts are possible. No further information is expected.


VAERS ID: 1574770 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-19
Onset:2021-01-19
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-08-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion missed, Eczema, Herpes zoster, Incorrect route of product administration, Maternal exposure during pregnancy
SMQs:, Drug abuse and dependence (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (narrow), Medication errors (narrow), Opportunistic infections (broad)

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

Write-up: Missed abortion; intravenous route of administration; maternal exposure during pregnancy; This regulatory authority prospective pregnancy case was reported by a consumer and describes the occurrence of ABORTION MISSED (Missed abortion) in a 27-year-old female patient who received mRNA-1273 (COVID 19 Vaccine Moderna) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 19-Jan-2021, the patient received first dose of mRNA-1273 (COVID 19 Vaccine Moderna) (unknown route) 1 dosage form. On 16-Feb-2021, received second dose of mRNA-1273 (COVID 19 Vaccine Moderna) (Intravenous) dosage was changed to 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 19-Jan-2021, the patient experienced MATERNAL EXPOSURE DURING PREGNANCY (maternal exposure during pregnancy). On 16-Feb-2021, the patient experienced INCORRECT ROUTE OF PRODUCT ADMINISTRATION (intravenous route of administration). On 20-Feb-2021, the patient experienced HERPES ZOSTER and ECZEMA. On 08-Mar-2021, the patient experienced ABORTION MISSED (Missed abortion) (seriousness criterion medically significant). The delivery occurred on an unknown date, which was reported as Unknown. For neonate 1, The outcome was reported as Spontaneous Abortion NOS. On 09-Mar-2021, HERPES ZOSTER and ECZEMA was resolving. At the time of the report, ABORTION MISSED (Missed abortion) had not resolved and MATERNAL EXPOSURE DURING PREGNANCY (maternal exposure during pregnancy) and INCORRECT ROUTE OF PRODUCT ADMINISTRATION (intravenous route of administration) had resolved. No concomitant and treatment information were reported by the reporter. This is a case of product exposure during pregnancy with associated AEs for this 27-year-old female. Based on the current available information and temporal association between the use of the product and the start date of the events Abortion missed, eczema and herpes zoster, a causal relationship cannot be excluded. RA reported an incorrect route of administration that could possible be a data entry error. More information is expected with translation.; Sender''s Comments: This is a case of product exposure during pregnancy with associated AEs for this 27-year-old female. Based on the current available information and temporal association between the use of the product and the start date of the events Abortion missed, eczema and herpes zoster, a causal relationship cannot be excluded. RA reported an incorrect route of administration that could possible be a data entry error. More information is expected with translation.


VAERS ID: 975155 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Kansas  
Vaccinated:2020-12-22
Onset:2021-01-20
   Days after vaccination:29
Submitted: 0000-00-00
Entered: 2021-01-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025J202A / 1 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamin
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: 01/20/2021- quantitative hcg 17, progesterone 0.2 01/22/2021- quantitative hcg 11, progesterone 0.1
CDC Split Type:

Write-up: LMP was 12/15/2020. Vaccine given on 12/22/2020. 3 positive pregnancy tests on 01/16/2021. Miscarried on 01/20/2021 as confirmed by serial quantitative hcg testing. Estimated 4-5WGA. Expectant management at home only


VAERS ID: 994135 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-19
Onset:2021-01-20
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-02-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 042120A / 1 LA / SYR

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Blood test, Exposure during pregnancy, Pain in extremity, Pregnancy test positive, Thrombosis, Ultrasound scan abnormal, Vaginal haemorrhage
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Malignancy related therapeutic and diagnostic procedures (narrow), Thrombophlebitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: 1/24/21 had ultrasound to confirm miscarriage
CDC Split Type:

Write-up: I am 38 years old with no history of medical problems. I do NOT have a history of miscarriages and have one healthy child who is 22 months old. On 1/13/21, I took a home pregnancy test which came back positive. At that time, I had a missed period but also had several common pregnancy symptoms such as bloating, acne, fatigue and tender breast. later that week, I called OB/Gyn and spoke to an RN to schedule my 8/9 week ultrasound and to inquiry about the vaccine during pregnancy since I had no clue whether it was recommended/safe or not. the RN, very confident and without any disclaimer, stated that hospital is recommending all of their pregnant patients to receive the vaccine. Obviously, I decided to trust this medical professional who was so confident in her response. My normal pregnancy symptoms continued. On 1/19/21, I was 5 weeks pregnant and received my first dosage of the vaccine. felt fine other than a sore left arm. on 1/20/21, I woke up with a lot of abdominal cramping and pain. It was new to me but assumed it was normal. My cramping and pain continued until 1/21/21. On 1/21/21, I woke up without the cramping and pain. But, I also noticed that my breast were no longer tender and my skin had completely cleared up. I became concerned but prayed everything was fine since my home pregnancy test was still positive. On 1/22/21, by cramps continued once again but more mild. My pregnancy symptoms seemed as if they were no longer present but remained hopeful. On 1/23/21, I woke up with light spotting that only lasted through the morning. Soon after, I started having extreme abdominal pains. I prayed everything was fine. The pain continued and became worse. That night, the pain was so bad that I just went to bed. Right before going to bed, I noticed I had started spotting again. A little heavier than in the morning. I made sure to lay on my left side, hoping it was normal in pregnancy. On 1/24/21, I woke up with heavy bleeding and clotting. I went to the doctor and got an ultrasound and blood test. I was told by the doctor at Hospital that I had a miscarriage.


VAERS ID: 1017013 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-01-19
Onset:2021-01-20
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-02-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ1686 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Pain, Pyrexia, Ultrasound scan
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, fluoxetine
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Sonogram showing 6 weeks 4 days embryonic demise, corresponding to approx. 01/20/2021 as the date of demise.
CDC Split Type:

Write-up: Gravida 1 with last menstrual period of 12/05/2020. Patient received 2nd dose of vaccine on 01/19/2021. Patient had fever and body aches the next day 1/20/2021 and subsequently (3 weeks later) was diagnosed with a miscarriage of pregnancy at 6 weeks 4 days, which exactly corresponds with the date of the vaccine and symptoms.


VAERS ID: 1067727 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2020-12-10
Onset:2021-01-20
   Days after vaccination:41
Submitted: 0000-00-00
Entered: 2021-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJO553 / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
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: Folic acid supplementation; Miscarriage; Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Date: 20210120; Test Name: scans or investigations; Result Unstructured Data: Test Result:Miscarriage at 8(ish) weeks; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021177542

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-202102171349489020, Safety Report Unique Identifier GB-MHRA-ADR 24780718. A 24-year-old female pregnant patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Batch/lot number: EJO553) via an unspecified route of administration on 10Dec2020 at single dose for COVID-19 immunization. Medical history included miscarriage in 2017, pregnancy, patient no longer pregnant at the time of reporting (as of 18Feb2021), folic acid supplementation. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Concomitant medication included folic acid for folic acid supplementation. The patient experienced maternal exposure during pregnancy on an unspecified date; miscarriage on 20Jan2021. Verbatim narrative: Her local pharmacist recommended that she flag this miscarriage even if it was not a reaction. She started bleeding at around 8 weeks and then was admitted to hospital. Did the medicine have an adverse effect on any aspect of the pregnancy: Unsure. Details of previous pregnancies: Had 2 children already (2018 and 2020) also had a miscarriage in 2017. Patient was exposed to the medicine Before pregnancy. Details of scans or investigations: Miscarriage at 8(ish) weeks. The patient underwent lab tests and procedures which included COVID-19 virus test: no - negative covid-19 test on an unspecified date; scans or investigations: miscarriage at 8(ish) weeks on 20Jan2021. The outcome of the event was recovered. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1450799 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-20
Onset:2021-01-20
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1419 / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion early, Body temperature, Headache, Nausea, Pain in extremity, Pyrexia, Vaccination site pain
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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: Bicornuate uterus
Allergies:
Diagnostic Lab Data: Test Date: 20210120; Test Name: fever; Result Unstructured Data: Test Result:39.6 Centigrade
CDC Split Type: DEPFIZER INC2021743324

Write-up: Questionable ADR/ temporal connection: 1st vacc on day 28 in a pregnancy that was unknowingly present at the time. Embryo died in the 6th week of gestation, development of a "wind-egg"/ Abortion early; 6 h after first vaccination: headache, fever up to 39.6?C, nausea, aching limbs, standing pain at injection site. Dead embryo found in 7th week of pregnancy.; 6 h after first vaccination: headache, fever up to 39.6?C, nausea, aching limbs, standing pain at injection site. Dead embryo found in 7th week of pregnancy.; 6 h after first vaccination: headache, fever up to 39.6?C, nausea, aching limbs, standing pain at injection site. Dead embryo found in 7th week of pregnancy.; 6 h after first vaccination: headache, fever up to 39.6?C, nausea, aching limbs, standing pain at injection site. Dead embryo found in 7th week of pregnancy.; 6 h after first vaccination: headache, fever up to 39.6?C, nausea, aching limbs, standing pain at injection site. Dead embryo found in 7th week of pregnancy.; This is a spontaneous report from a non-contactable consumer downloaded from a regulatory authority-WEB. The Regulatory Authority report number is DE-PEI-CADR2021019938, Safety Report Unique Identifier DE-PEI-2021010206. A 37-year-old female patient received BNT162B2 (COMIRNATY, solution for injection, Batch/Lot Number: EL1419), intramuscular on 20Jan2021 (at the age of 37 years old) as dose 1, 0.3 mL single for COVID-19 immunisation. Medical history included Uterus bicornis. The patient''s concomitant medications were not reported. The patient experienced questionable adr or temporal connection on 20Jan2021, 1st vaccination on day 28 in a pregnancy that was unknowingly present at the time. Embryo died in the 6th week of gestation, development of a "wind-egg"/ abortion early. 6 h after first vaccination, on 20Jan2021, the patient experienced headache, fever up to 39.6?c, nausea, aching limbs, standing pain at injection site. Dead embryo was found in 7th week of pregnancy. The patient was 1 Month pregnant at the onset of the event. The pregnancy resulted in spontaneous abortion. The outcome of the events abortion early was recovered with sequelae on 20Feb2021 and for pyrexia was recovered with sequelae on 21Feb2021 while the outcome of the rest of the events was recovered with sequelae on an unspecified date. PEI assessed the causality between Comirnaty and the events as B. No follow-up attempts are possible. No further information is expected.


VAERS ID: 967169 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-01-16
Onset:2021-01-21
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-01-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3248 / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Exposure during pregnancy, Ultrasound scan, Urine analysis
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: Prenatal vitamins
Current Illness: N/A
Preexisting Conditions: Asthma
Allergies: N/A
Diagnostic Lab Data: Blood, urine, and ultrasound on 1/21/2021
CDC Split Type:

Write-up: Miscarriage? around 7 weeks pregnant at the time of vaccine, estimated delivery date was 8/19/2021


VAERS ID: 970490 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Texas  
Vaccinated:2020-12-30
Onset:2021-01-21
   Days after vaccination:22
Submitted: 0000-00-00
Entered: 2021-01-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: My second first dose dose took place on 12/30 and second on 1/19. I had a miscarriage on 1/21.
Current Illness: Asthma
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage


VAERS ID: 980140 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Mississippi  
Vaccinated:2021-01-20
Onset:2021-01-21
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-01-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR

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? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Unexplained Pregnancy loss


VAERS ID: 1010113 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2021-01-07
Onset:2021-01-21
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-02-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, Diclegis
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Fetal U/S on 2/4
CDC Split Type:

Write-up: Miscarriage - first vaccine at 10 weeks and 3 days with prior proof of heartbeat/movement, second vaccine at 13 weeks and 3 days; learned of miscarriage at 14 weeks 3 days with measurements of 12 weeks 3 days on U/S


VAERS ID: 1026866 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-01-01
Onset:2021-01-21
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-02-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 039K20-2A / 1 LA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011M20A / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound scan abnormal
SMQs:, Malignancy related therapeutic and diagnostic 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? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Pre natal Vitamins
Current Illness: None
Preexisting Conditions: Migraines
Allergies: No
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage- received 1st dose of vaccine when approximately 4 weeks pregnant on 1/6/21. 1st ultrasound at 7 weeks on 1/26/21. Intrauterine pregnancy with yolk sack but no fetal pole seen. 2nd dose of vaccine at approximately 9 weeks pregnant on 2/3/21. Diagnosis of miscarriage on ultrasound on 2/8/21. Due date should have been 9/13/21


VAERS ID: 1058428 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Connecticut  
Vaccinated:2021-01-21
Onset:2021-01-21
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-02-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 013L20A / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Body temperature increased, Chills, Human chorionic gonadotropin negative, Nausea, Pain, Pyrexia, Sleep disorder, Ultrasound antenatal screen abnormal
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (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), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: COVID 19 1st vaccine; unilateral adenopathy (filed report)
Other Medications: Prenatal
Current Illness: n/a
Preexisting Conditions: hypertension
Allergies: erythromycin (questionable)
Diagnostic Lab Data: 27th; HCG levels 12 1/28th, 4th 1/29th. 27th jan ultra sound; no fetus.
CDC Split Type: vsafe

Write-up: 1/21 vaccination By that evening, I started having chills by 5pm. Began to have body aches; 7pm. Low Grade fever increased to 102 overnight. I didn''t sleep at all to no avail with Tylenol and Motrin. Nauseous. 1/22 pregnancy test; positive By Friday evening, symptoms started to dissipate. 1/26 Miscarried; 4 weeks 3 days pregnant 1st pregnancy


VAERS ID: 1163739 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: Kentucky  
Vaccinated:2021-01-06
Onset:2021-01-21
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-04-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025J20A / 1 LA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 030L20A / 2 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Caesarean section, Exposure during pregnancy, Foetal heart rate decreased, Foetal hypokinesia, Premature delivery, Ultrasound foetal abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow)

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, 55 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: S/C Levonox 40 mcg daily Tab Folic Acid 5mg daily Tab Prenatal Vitamin 1 tab daily Tab baby aspirin 81mg daily Tab Colace 1 tab daily
Current Illness: None
Preexisting Conditions: Thrombophila A1 deficiency
Allergies: Atropine
Diagnostic Lab Data: Very hi liver enzymes Clotting cascades out of range Low glucose Hi bilirubin
CDC Split Type:

Write-up: done on infant in uterine showed for the first time: Liver calcification noted measuring 5.9 x 4.2 x 1.7 mm. I git pregnant post ablation done in November 2019. The pregnancy was pretty normal. I have been considered hi risk due to my age, having an ablation and the throbophilia. At that point I had an done every 4 weeks since I was 18 weeks pregnant. Due date is 08/05/2021. The calcification of the liver has been seen in every since. I was scheduled to see a Neurologist on 03/18. On 03/16 baby stopped moving. Went to ER. Heart rate of fetuses was declining. An emergent C-Section was done. When baby came out she was in DIC due to acute hepatic failure. She received multiple different blood products along with Antibiotics, IVIG, IV Dopamine drip, IV lasix, and TPN. She was on the ventilator, had a central line, art line, multiple IV?s and NG tube. Birth weight was 1770 grams.


VAERS ID: 1038910 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-19
Onset:2021-01-21
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-02-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK9788 / 2 - / 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: DEPFIZER INC2021126884

Write-up: Miscarriage; This is a spontaneous report from a non-contactable consumer downloaded from the Regulatory Authority-WEB DE-PEI-CADRPEI-2021013246 and received via Regulatory Authority. A 25-year-old female patient (pregnant) received second dose of BNT162B2 (COMIRNATY)Lot number EK9788, Intramuscular at 0.3 ml, single on 19Jan2021 for COVID-19 immunisation. Medical history and concomitant medications were not reported. The pregnant patient previously received first dose of BNT162B2 (lot number EK9788) on 29Dec2020. On 21Jan2021 after vaccination the patient developed Miscarriage. The outcome of Miscarriage was resolving. The event was serious with other medically important condition. No follow-up attempts possible. No further information expected.


VAERS ID: 1076348 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2020-12-18
Onset:2021-01-21
   Days after vaccination:34
Submitted: 0000-00-00
Entered: 2021-03-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ0553 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, COVID-19, Drug ineffective, Human chorionic gonadotropin, Maternal exposure during pregnancy, SARS-CoV-2 test
SMQs:, Lack of efficacy/effect (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (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: BISOPROLOL FUMARATE; CARBIMAZOLE; CYCLIZINE; FLECAINIDE; FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Arrhythmia; Folic acid supplementation; Heart rate; Hyperemesis; Hyperthyroidism; Mood change; Pregnancy (4 years ago)
Allergies:
Diagnostic Lab Data: Test Name: HCG blood test; Result Unstructured Data: Test Result:confirmed; Test Name: COVID-19 virus test; Test Result: Positive ; Test Date: 20201101; Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021185970

Write-up: miscarriage; Maternal exposure during pregnancy; SARS-CoV-2 infection; SARS-CoV-2 infection/COVID-19; This is a spontaneous report from a contactable consumer received from the Regulatory Agency (RA). The regulatory authority report number is (GB-MHRA-WEBCOVID- 202102191629201180) with Safety Report Unique Identifier (GB-MHRA-ADR 24795367). A 32-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ0553), via an unspecified route of administration on 18Dec2020 at a single dose for COVID-19 immunisation. Medical history included mood change, folic acid supplementation, arrhythmia, hyperemesis, hyperthyroidism and "heart rate". The patient has been advised to shield. The patient had previous healthy pregnancy 4 years ago (2017). The patient has not had symptoms associated with COVID-19. The patient is not enrolled in clinical trial. Concomitant medication included bisoprolol fumarate from 01Jul2018 to 15Jan2020 for heart rate, carbimazole from 01Jul2018 to 15Jan2021 for hyperthyroidism, cyclizine from 18Jan2021 to 21Jan2021 for hyperemesis, flecainide from 01Jul2018 for arrhythmia and folic acid for folic acid supplementation. The patient was exposed to the medicine before pregnancy. On an unspecified date, the patient experienced miscarriage and maternal exposure during pregnancy. On 21Jan2021, the patient experienced SARS-CoV-2 infection and COVID-19. It was reported that the patient had a miscarriage the day after her positive COVID test (unspecified date). It was unsure if the medicine had an adverse effect on any aspect of the pregnancy. The patient had an HCG blood test: confirmed on an unspecified date. On 21Nov2020, the patient had a negative (no - negative COVID-19 test) result. The events were considered serious, medically significant by the regulatory authority. The patient recovered from SARS-CoV-2 infection/COVID-19 on 03Feb2021 (also reported as 01Feb2021). The outcome of the remaining events was unknown. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1152998 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-14
Onset:2021-01-21
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-03-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1491 / 1 - / OT

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

Life Threatening? Yes
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: Neuromyelitis optica
Allergies:
Diagnostic Lab Data:
CDC Split Type: PTPFIZER INC2021323092

Write-up: Aborted pregnancy; vaginal blood loss; This is a spontaneous report downloaded from the Regulatory Authority-WEB [PT-INFARMED-E202103-682]. A contactable nurse reported that a 29-year-old female patient received first dose of bnt162b2 (COMIRNATY; lot EL1491), intramuscular on 14Jan2021 at 0.3 mL, single for COVID-19 immunisation. Medical history included neuromyelitis optica. The patient''s concomitant medications were not reported. On 21Jan2021, the patient experienced aborted pregnancy. She didn''t know that she was was pregnant and took the first dose of Comirnaty. She had vaginal blood loss for four days about eight days after the vaccine. The event appeared 7 days after the start of the administration of the suspected drug, with an approximate duration of 4 days. The event involved the reproductive system and was life-threatening. Evolution of event was cure. Outcome of events was recovered on 25Jan2021. Relatedness of drug to event assessed by reporter as possible (unknown method of assessment).


VAERS ID: 1245819 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-21
Onset:2021-01-21
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Gingival pain, Hypoaesthesia oral, Laboratory test, Maternal exposure during pregnancy, Mouth swelling, Oral mucosal erythema
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Oropharyngeal allergic conditions (narrow), Gingival disorders (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (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? No
Previous Vaccinations:
Other Medications: CITALOPRAM; DICLOFENAC; FOLIC ACID; LEVOTHYROXINE; MISOPROSTOL
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Hyperthyroidism
Allergies:
Diagnostic Lab Data: Test Name: lab test; Result Unstructured Data: Test Result:Missed miscarriage
CDC Split Type: GBPFIZER INC2021392065

Write-up: Sore gums; Tongue feels slightly numb also; Dark red dots on inside of cheeks; Swollen mouth; miscarriage; Maternal exposure during pregnancy; This is a spontaneous report from a contactable consumer received from the Regulatory Agency (RA). Regulatory authority report number is GB-MHRA-WEBCOVID-202104071718347260, Safety Report Unique Identifier is GB-MHRA-ADR 25107647. A 30-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration (age at vaccination was 30 years) on 21Jan2021 (Lot number and expiry date not reported) as single dose, and second dose via an unspecified route of administration on 01Apr2021 (Lot number and expiry date not reported) as single dose for COVID-19 immunization. Medical history included hyperthyroidism from an unknown date and unknown if ongoing. Patient was pregnant at time of vaccination but no longer pregnant at the time of reporting. Concomitant medications included citalopram taken for anxiety, start and stop date were not reported; diclofenac taken for abortion spontaneous from 30Mar2021 to 30Mar2021; folic acid taken for vitamin supplementation, pregnancy from 06Feb2021 to 28Mar2021; levothyroxine taken for hyperthyroidism, start and stop date were not reported; and misoprostol taken for abortion spontaneous from 30Mar2021 to 30Mar2021. The patient experienced miscarriage on 27Mar2021 with outcome of recovering, maternal exposure during pregnancy on 21Jan2021 with outcome of unknown, swollen mouth on 04Apr2021 with outcome of not recovered, sore gums on an unspecified date with outcome of unknown, tongue feels slightly numb also on an unspecified date with outcome of unknown, and dark red dots on inside of cheeks on an unspecified date with outcome of unknown. The patient underwent lab tests and procedures which included laboratory test: missed miscarriage. The events were reported as serious, medically significant. Patient has not tested positive for COVID-19 since having the vaccine. It was unsure if patient had had symptoms associated with COVID-19. Patient had not had a COVID-19 test. Patient was not enrolled in clinical trial. Patient was not currently breastfeeding. Inside of mouth feels swollen including cheeks. Dark red dots on inside of cheeks. Sore gums. Tongue feels slightly numb also. Info regarding my miscarriage: I found out I was pregnant on 04Feb2021. On 27Mar2021 I found out that I had a missed miscarriage. It was unsure if the medicine have an adverse effect on any aspect of the pregnancy. Patient was exposed to the medicine first-trimester (1-12 weeks). Details of scans or investigations: Missed miscarriage found at 11 weeks. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1029307 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-01-21
Onset:2021-01-22
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-02-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN9581 / 1 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: Penicillin
Diagnostic Lab Data: Viability ultrasound on 2/12/2021
CDC Split Type:

Write-up: Missed abortion Date of last period December 1, 2020 (34 day cycle) Fetus measured 6 weeks and 4 days on 2/12/2021, but I was expected to be at 9 weeks 4 days. No heart beat. Therefore, estimated date of fetal demise is 1/22/2021 First pregnancy, estimated date of delivery 09/13/2021 Scheduled for D&E on 2/17/2021


VAERS ID: 1075754 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-21
Onset:2021-01-22
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-03-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 042L20A / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Fatigue, Human chorionic gonadotropin, Pain in extremity, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Levothyroxine; prenatal vitamins
Current Illness: -adverse symptoms from December 24''s first dose of COVID vaccine - headache - three hours and arm soreness that lasted until the 28th. -no other acute symptoms
Preexisting Conditions: no
Allergies: no
Diagnostic Lab Data: These were at Medical Center I was having serial beta HCGs done - I had my first one on the 19th of January - 170 MIU per ml; 21st - 250 MIU per ml; 25th of January - 330 MIU per ml; 27th of January - 404.8 MIU per ml; 29th of January - 478 MIU per ml;, I think I had one the first or second of February but don''t have the results - think that was lower. February 8 - 2 MIU per ml I had my thyroid test done on the January 19th - my TSH was 3.85 UIU per ml; I had a free T4 - 1.35 ng/dl
CDC Split Type: vsafe

Write-up: I had some arm soreness that started the morning after (22nd) and that lasted until the 27th of January....it got better each day. I had fever to 102 that started on the 22nd. The fever ended on 23rd. I took Tylenol - it didn''t help on the 22nd but by 23rd it did. I felt fatigue -22nd and went away on 24th. I miscarried 27th-29th -30th- that timeframe. The miscarriage prompted care. I went to Medical Center. I was not pregnant at time first vaccination. Estimated date of delivery had been - September 22, 2021; I have no prior pregnancy history.


VAERS ID: 1198333 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Oregon  
Vaccinated:2020-12-23
Onset:2021-01-22
   Days after vaccination:30
Submitted: 0000-00-00
Entered: 2021-04-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 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: none
Current Illness: no
Preexisting Conditions: none
Allergies: penicillin
Diagnostic Lab Data: Saw a midwife and had HCG tracked and blood drawn - a week a before and a week after the 22nd I had labwork tracking the miscarriage
CDC Split Type: vsafe

Write-up: I had a miscarriage on January 22, 2021


VAERS ID: 1481396 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: New York  
Vaccinated:2021-01-21
Onset:2021-01-22
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-07-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029L20A / 2 LA / -

Administered by: Work       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Exposure during pregnancy, Full blood count, Gynaecological examination, Human chorionic gonadotropin abnormal, Metabolic function test, Ultrasound scan vagina abnormal, Vaginal haemorrhage
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Malignancy related therapeutic and diagnostic procedures (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (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: prenatal vitamins only
Current Illness: none
Preexisting Conditions: none
Allergies: sulfa drug intolerance, allergy to shellfish
Diagnostic Lab Data: 7/17/21 serum HCG, BMP, CBC, vaginal ultrasound, pelvic speculum exam
CDC Split Type:

Write-up: Pt with no significant medical history, received dose 1 Moderna during unknown pregnancy. Her second dose of Moderna was on 1/21/21, she began experiencing vaginal bleeding at midnight on 1/22/21. Her estimated delivery date was 9/21/2020. She experienced a full spontaneous abortion. Pt is now presenting to ED pregnant for the second time at 5 weeks with vaginal bleeding x2 days with abdominal cramping. Pt diagnosed with threatened miscarriage, pregnancy viability status to be determined with further monitoring.


VAERS ID: 1396861 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-19
Onset:2021-01-22
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-06-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK9788 / 2 - / OT

Administered by: Other       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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: Beta-HCG; Result Unstructured Data: Test Result:decreased/drop
CDC Split Type: DEPFIZER INC2021625837

Write-up: Early abortion (miscarriage) in the 6th week of pregnancy; This is a spontaneous report from a non-contactable consumer downloaded from a regulatory authority-WEB, regulatory authority number is DE-PEI-CADR2021017912. A 25-year-old pregnant female patient received BNT162B2 (COMIRNATY, solution for injection), dose 2 intramuscular on 19Jan2021 (Batch/Lot Number: EK9788) as 2nd dose, 0.3 ml single dose for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient was previously administered with first dose of BNT162B2 (COMIRNATY, lot: unknown) as 0.3 ml, single dose for COVID-19 immunisation and experienced maternal exposure during pregnancy. On 22Jan2021, the patient experienced early abortion (miscarriage) in the 6th week of pregnancy. The patient underwent lab tests and procedures which included Beta-HCG (human chorionic gonadotropin): decreased/dropped on an unspecified date. Outcome of event was recovered with sequel (as reported). Event assessment: Comirnaty/event/PEI /Result of Assessment:D. Sender''s comments: outpatient treatment, beta hCG drop. No follow-up attempts are possible. No further information is expected.; Reporter''s Comments: outpatient treatment, beta hCG drop.


VAERS ID: 1452003 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-02
Onset:2021-01-22
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain lower, Abortion spontaneous, Haemorrhage, Maternal exposure during pregnancy, Retroplacental haematoma
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: ESPFIZER INC2021753039

Write-up: Retroplacental hematoma; spontaneous Abortion; pain in the hypogastric region; slight bleeding; finds out that is pregnant; This is a spontaneous report from a contactable pharmacist downloaded from the WEB, regulatory authority number ES-AEMPS-909043. An adult female patient received bnt162b2 (COMIRNATY), dose 2 via an unspecified route of administration on 02Feb2021 (Batch/Lot Number: Unknown) as DOSE 2, SINGLE and dose 1 via an unspecified route of administration on 12Jan2021 (Batch/Lot Number: Unknown) as DOSE 1, SINGLE, both for covid-19 immunisation. The patient''s medical history and concomitant medications was not reported. Patient who receives the first dose of Comirnaty on 12Jan2021 and 10 days later finds out that is pregnant. Decides to administrate the second dose on 02Feb2021 and on 11Feb2021 after noticing pain in the hypogastric region, accompanied by slight bleeding, she decided to go to the emergency room and after evaluation by the Gynecology Service, a retrochorial hematoma and absence of a fetal heartbeat were seen, diagnosing spontaneous abortion in the first trimester. Seriousness Criteria was hospitalization and medical significant. The outcome of pain in the hypogastric region, accompanied by slight bleeding was unknown, the outcome of spontaneous Abortion was recovered on 11Feb2021, the outcome of Retroplacental hematoma recovered on an unknown date. No follow-up attempts are possible. No further information is expected.


VAERS ID: 995875 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Vermont  
Vaccinated:2021-01-09
Onset:2021-01-23
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-02-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK9211 / 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? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: Sulfa Shellfish
Diagnostic Lab Data: HCG TRACT
CDC Split Type: vsafe

Write-up: Miscarriage Estimated date of delivery 09/12/2021 I was give IV fluids


VAERS ID: 1108773 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Indiana  
Vaccinated:2020-12-26
Onset:2021-01-23
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-03-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1284 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK9231 / 2 RA / IM

Administered by: Work       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: Wellbutrin XL 300 mg once daily prenatal vit daily
Current Illness: none
Preexisting Conditions: depression
Allergies: none
Diagnostic Lab Data: Miscarriage confirmed on 1/25/21
CDC Split Type:

Write-up: I suffered a miscarriage at 7 weeks 4 days. Miscarriage occurred on 1/23/21. Vaccination 1 was on 12/26/20 & Vaccination 2 was 1/12/21


VAERS ID: 1122111 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Maine  
Vaccinated:2021-01-06
Onset:2021-01-23
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-03-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1284 / 2 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Sertraline 50 mg
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: Environmental only
Diagnostic Lab Data: Ultrasounds on 2/8 and 2/18, multiple HcG levels confirming unviable pregnancy
CDC Split Type:

Write-up: Received both 1st and 2nd dose of Pfizer vaccine before learning that I was pregnant. Conception likely occurred between the two doses, but official pregnancy dating unclear. Ultrasound demonstrated unviable pregnancy on 2/8/21.


VAERS ID: 975126 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-01-20
Onset:2021-01-25
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-01-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3249 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Dizziness, Exposure during pregnancy, Headache, Human chorionic gonadotropin, Hypothyroidism, Migraine, Nausea, Vaginal haemorrhage
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypothyroidism (narrow), Vestibular disorders (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: butalbital-acetaminophen-caffeine, MVI, sumatriptan
Current Illness: Pregnancy - 1st trimester, just confirmed; history of miscarriages;
Preexisting Conditions: history of miscarriages; anemia, migraines, sinus arrhythmia
Allergies: NKDA
Diagnostic Lab Data: HCG, QUANTITATIVE; Status: Final result Visible to patient: Yes (MyChart) Dx: Spotting in early pregnancy Human Chorionic Gonadotropin Quantitative <5 mIU/mL 12High
CDC Split Type:

Write-up: G2P0, 5w5d; The patient is calling with vaginal bleeding in pregnancy. Calling with c/o dizziness with headache; Has a history of migraines; States she has subclinical hypothyroidism. Has tried Tylenol 500 mg for headache that worked for a little while; She denies vomiting, but does have nausea; Will try to increase water and protein intake; Will let us know if she gets worse/vision changes and will check in with PCP as they wanted to do a VV if dizziness got worse. Bleeding continued into following day. Documented as likely / threatened miscarriage.


VAERS ID: 987914 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Iowa  
Vaccinated:2021-01-22
Onset:2021-01-25
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-01-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK4176 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Back pain, Blood test, Exposure during pregnancy, Ultrasound scan
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), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? Yes
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: Zyrtec, 200 mg Progesterone
Current Illness: Subchorionic hematoma, diagnosed by ultrasound on 1/19/2021
Preexisting Conditions: GERD
Allergies: None
Diagnostic Lab Data: Bloodwork and Ultrasound done 1/26/2020 in ER after miscarriage, have follow up appt with OBGYN on 2/15
CDC Split Type:

Write-up: Received COVID vaccine on Friday afternoon, 1/22, developed some slight abdominal cramping 1/24 and 1/25, had severe abdominal and back pain resulting in miscarriage evening of 1/25. Estimated date of delivery: August 27, 2020 Also had known subchorionic hematoma, diagnosed on 1/19 via ultrasound at physician''s (OBGYN) office


VAERS ID: 997660 (history)  
Form: Version 2.0  
Age: 46.0  
Sex: Female  
Location: Utah  
Vaccinated:2021-01-19
Onset:2021-01-25
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-02-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025L20A / 1 RA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abortion induced, Erythema, Skin irritation, Swelling
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (broad), 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? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: My right arm presented with a large round lump that was red, irritated and bumpy. The following day, it continued to grow to the size of a baseball. It was warm to the touch and sensitive. As of today, the swelling has gone down significantly (although it''s still swollen) it is still visibly red, however, no longer sensitive to the touch.


VAERS ID: 1018222 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Indiana  
Vaccinated:2020-12-30
Onset:2021-01-25
   Days after vaccination:26
Submitted: 0000-00-00
Entered: 2021-02-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Laboratory test, Myalgia, Pyrexia, Ultrasound antenatal screen, Vaginal haemorrhage
SMQs:, Rhabdomyolysis/myopathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Eosinophilic pneumonia (broad), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, Escitalopram
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: I had lab work done prior to having a D&C procedure on Feb. 4th. The "remains" were sent to pathology at Hospital.
CDC Split Type:

Write-up: I found out I was pregnant the day after receiving the first dose of the COVID-19 vaccine. My last period was on December 8th and I received the vaccine on Dec 30th. I developed a fever and muscle aches after the first dose, but was managed with Tylenol. I received the second dose on January 22nd and again developed a fever that was managed by Tylenol. I began having vaginal bleeding on 24th. I had an ultrasound revealing a heartbeat on the 25th. After continually bleeding, another ultrasound a week later on Feb. 2nd confirmed a miscarriage. I''ve had two healthy pregnancies prior to this one.


VAERS ID: 1046322 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-01-05
Onset:2021-01-25
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

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

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

Write-up: Missed abortion - received first shot while pregnant (did not know), missed abortion of ~5 weeks gestational age, diagnosed Feb 2021


VAERS ID: 1078165 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-01-21
Onset:2021-01-25
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-03-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 AR / SYR

Administered by: Private       Purchased by: ?
Symptoms: Caesarean section, Exposure during pregnancy, Foetal distress syndrome, Hypertension, Pre-eclampsia, Premature delivery, Protein urine present, Proteinuria
SMQs:, Acute renal failure (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Hypertension (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Chronic kidney disease (broad), Proteinuria (narrow), Tubulointerstitial diseases (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 4 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, baby aspirin
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Blood pressure high and urine test showed proteins in urine. 1/25/21
CDC Split Type:

Write-up: At routine 38 week doctor appointment, had high blood pressure. Upon re-check, it was still high and also had protein in the urine. Diagnosed with pre-eclampsia despite never having issues with high blood pressure and none of the associated risk factors. Went straight to labor and delivery and upon monitoring, baby was in distress. Heart rate did come back up; she was born that evening by c-section. Original due date was February 5, 2021 (birth date was January 25). Birth weight was 5 lbs 12 oz.


VAERS ID: 1333918 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-01-06
Onset:2021-01-25
   Days after vaccination:19
Submitted: 0000-00-00
Entered: 2021-05-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK5730 / 1 AR / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK4176 / 2 AR / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: None
Preexisting Conditions: Well controlled asthma, prn albuterol
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Vaccines administered 12/19/2020 and 01/06/2021. Second vaccine determined to be done in 3rd week of pregnancy (prior to positive pregnancy test). Miscarriage occurred 01/25/2021 at 6 weeks. Otherwise healthy, prenatally-optimized 34 yo woman without personal or family history of miscarriage or pregnancy complications.


VAERS ID: 1591174 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-01-22
Onset:2021-01-25
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-08-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK4176 / 1 RA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9264 / 2 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Dysuria, Genital pain, Herpes virus test, Treponema test negative, Uterine dilation and curettage
SMQs:, Termination of pregnancy and risk of abortion (narrow), Sexual dysfunction (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Levothyroxine
Current Illness:
Preexisting Conditions:
Allergies: Amoxicillin Doxycycline
Diagnostic Lab Data: Herpes 1/27/21 Negative Syphilis 1/27/21 Negative HGC levels 5/6/21 and 5/8/21 to confirm miscarriage DNC procedure 5/20/21
CDC Split Type:

Write-up: Just days after my first vaccine, I ended up with genital sores. It started off by just hurting to pee. The pain grew worse so I made an appointment with my doctor thinking that I just had a bladder infection. She had taken a look down there and in fact there were sores. She tested me for several sexual transmitted diseases. All of those test came back negative. She then prescribed me an anabiotic which cleared it up within the next 10 days or so. Was the most miserable experience. Miscarriage 5/8/21 - day of last period was February 18, 2021 meaning I was pregnant shortly after my second shot of the vaccine. I was 10 weeks along.


VAERS ID: 1021706 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-13
Onset:2021-01-25
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-02-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EE8492 / 1 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: FOLIC ACID; VITAMIN D [COLECALCIFEROL]
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: COVID-19
Allergies:
Diagnostic Lab Data: Test Date: 20210122; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Pending; Test Date: 20210125; Test Name: Nasal Swab; Test Result: Negative
CDC Split Type: GBPFIZER INC2021080916

Write-up: Miscarriage at 5w4d gestation; This is a spontaneous report from a contactable other healthcare professional (patient). A 30-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EE8492), via an unspecified route of administration on 13Jan2021 13:30 as a single dose in left arm for COVID-19 immunization. Medical history included diagnosed with COVID-19 prior to vaccination. No known allergies. Concomitant medications included folic acid and vitamin D within two weeks of vaccination. Patient''s last menstrual period was on 18Dec2020, she was pregnant at the time of vaccination and did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The most recent COVID-19 vaccine was administered in a hospital. The patient experienced a miscarriage at 5 weeks 4 days gestation on 25Jan2021. Gestation period when the event was observed in the fetus was also reported as 4 weeks. The adverse event resulted in a doctor''s clinic visit and emergency room/urgent care visit. The patient underwent lab tests and procedures which included nasal swab: pending result on 22Jan2021 and negative on 25Jan2021. Patient has been tested for COVID-19 post-vaccination (PCR lateral flow test). It was unknown if treatment was received for the adverse event. Outcome of the event was unknown.; Sender''s Comments: Based on available information, a possible contributory role of the subject product, BNT162B2 vaccine, cannot be excluded for the reported event of miscarriage due to temporal relationship. However, the reported event may possibly represent intercurrent medical condition in this patient. There is limited information provided in this report. This case will be reassessed once additional information is 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: 1161758 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-25
Onset:2021-01-25
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1484 / 2 LA / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Antibody test, Blood test, Body temperature, Bone pain, Dyspnoea, Echocardiogram, Fatigue, Headache, Oxygen saturation, Oxygen saturation decreased, Pulmonary physical examination, Pyrexia
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Osteonecrosis (broad), Termination of pregnancy and risk of abortion (narrow), Respiratory failure (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (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: DELTACORTENE; ZITHROMAX; ASPIRINETTA
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210125; Test Name: antibodies; Result Unstructured Data: Test Result:340; Test Date: 20210215; Test Name: antibodies; Result Unstructured Data: Test Result:5400; Test Name: blood tests; Result Unstructured Data: Test Result:increased pulmonary pressure; Test Date: 20210125; Test Name: body temperature; Result Unstructured Data: Test Result:febricula; Test Name: echocardiogram; Result Unstructured Data: Test Result:increased pulmonary pressure; Test Date: 20210125; Test Name: oxygen saturation; Result Unstructured Data: Test Result:desaturation; Test Name: pulmonary examination; Result Unstructured Data: Test Result:increased pulmonary pressure
CDC Split Type: ITPFIZER INC2021281097

Write-up: Miscarriage; headache; fatigue; bone pain; febricula; desaturation/Oxygen saturation low; breathlessness; The initial safety information received was reporting only non-serious adverse drug reaction(s), Upon receipt of follow-up information on 19Mar2021, this case now contains serious adverse reaction(s). Information processed together. This is a spontaneous report from a contactable other healthcare professional downloaded from the Regulatory Authority-WEB IT-MINISAL02-695266. This case was split to capture events that occurred after first dose. This is the first of two reports. A 37-year-old female pregnant patient received bnt162b2 (COMIRNATY; Solution for injection), dose 2 intramuscular, administered in Left arm on 25Jan2021 (Batch/Lot Number: EL1484) 0.3 ml as single dose for covid-19 immunisation. The patient medical history was not reported. Concomitant medication(s) included prednisone (deltacortene 25 mg); azithromycin (zithromax); acetylsalicylic acid (aspirinetta) and calcium mefolinate (prefolic). The patient historical vaccine included bnt162b2 (COMIRNATY), (1st dose), on 03Jan2021 for covid-19 immunisation and had arm pain. It was reported on 25Jan2021 patient had fever, bone pain, headache Subsequently desaturation/ Oxygen saturation low, breathlessness, fatigue, febricula Update of 15Mar2021: miscarriage; The patient underwent pulmonary examination, echocardiogram, blood tests which showed increased pulmonary pressure. Therapeutic measures were taken for all events. The outcome of the events was reported as recovered on 12Mar2021. Reporter''s comments: After the 1st dose (01Mar2021) only arm pain, after 2nd dose initially bone pain, fever, headache 340 antibodies, subsequently about 15 days, after pregnancy discovery (15Feb2021), 5400 antibodies with desaturation, breathlessness, febricula and headache.


VAERS ID: 1170735 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-05
Onset:2021-01-25
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-04-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 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? 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: PTPFIZER INC2021067380

Write-up: Spontaneous abortion; This is a spontaneous report from a contactable nurse (patient). This nurse reported information for both mother and fetus/baby. This was a maternal report. A pregnant female patient of an unspecified age received BNT162B2 (COMIRNATY, Solution for injection), dose 1 via an unspecified route of administration, on 05Jan2021 (Lot number: UNKNOWN) as 0.3 mL, single for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient was pregnant at the time of vaccination. The patient reported she was 7 weeks pregnant at the time of vaccination. Upon Follow-up on 22Mar2021, the nurse reported that she suffered a spontaneous abortion at 8 gestation weeks, one day before receiving the 2nd dose of BNT162B2 (COMIRNATY), on 25Jan2021. The nurse additionally reported that at the 1st dose gestation period was approximately 5 weeks. The outcome of the event was unknown. Information on the lot/batch number has been requested. Follow-up (22Mar2021): New Information received from the same contactable nurse (patient) includes: Added new event (spontaneous abortion) and clinical information. Information on the lot/batch number has been requested.; 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 spontaneous abortion cannot be totally excluded. This case will be reassessed once additional information is available.


VAERS ID: 1378645 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-14
Onset:2021-01-25
   Days after vaccination:11
Submitted: 0000-00-00
Entered: 2021-06-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM0477 / 1 LA / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Asymptomatic COVID-19 (COVID-19 has passed)
Allergies:
Diagnostic Lab Data:
CDC Split Type: ESPFIZER INC2021590902

Write-up: miscarriage; This is a spontaneous report from a contactable physician (patient) downloaded from the regulatory authority, regulatory authority number ES-AEMPS-750101. A 34-year-old female patient received BNT162B2 (COMIRNATY, Solution for injection), dose first intramuscular, administered in arm left on 14Jan2021 (Lot Number: EM0477) as single dose for covid-19 immunisation. Medical history included asymptomatic serology of COVID-19 and COVID-19 has passed. The patient received the 1st dose of vaccine without knowing the gestational stage since it was 3 weeks according to last menstrual period. 11 days later the patient suffered a miscarriage on 25Jan2021. Reasons for the patient''s vaccination reported as Health professional or personnel of socio-health or essential center. The outcome of the event was resolved on 28Jan2021. No follow-up attempts possible. No further information expected.


VAERS ID: 1883059 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2021-01-25
Onset:2021-01-25
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-11-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion induced, Maternal exposure timing unspecified, Trisomy 13
SMQs:, Congenital, familial and genetic disorders (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 0000-00-00
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: DEPFIZER INC202101575119

Write-up: Trisomy 13 Detected and Confirmed During Pregnancy; Drug exposure during pregnancy; termination of pregnancy in the course; This is a spontaneous report from a non-contactable consumer. This consumer reported information for both mother and fetus. This is a fetus report. The first report (mother case) was downloaded from the regulatory authority number DE-CADR2021184704. A fetus patient received bnt162b2 (COMIRNATY), transplacental on 25Jan2021 (Lot number was not reported) as dose number unknown, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On 01May2021 the trisomy 13 detected and confirmed during pregnancy. The patient was hospitalized for maternal drug exposure and trisomy 13 in 2021. The mother was 1 months pregnant at the onset of the event. The mother underwent elective termination. The fetal outcome is congenital anomaly. The patient had termination of pregnancy in the course in 2021. The outcome of trisomy 13 was reported as recovered on 11May2021. The patient died on an unspecified date in 2021. It was not reported if an autopsy was performed. Assessment: Trisomy/ Exposure during pregnancy/ Comirnaty/ D No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Sender''s Comments: Linked Report(s) : DE-PFIZER INC-202101523717 mother case; Reported Cause(s) of Death: Drug exposure during pregnancy; termination of pregnancy in the course


VAERS ID: 1008618 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-01-25
Onset:2021-01-26
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-02-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025L20A / UNK LA / SYR
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 43L20A / UNK LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: None known
Diagnostic Lab Data: Ultrasound on 1/27/2021 and 2/3/2021. Blood test on 2/3/2021.
CDC Split Type:

Write-up: I was pregnant, embryo estimated 6 weeks gestation. I started having spotting approximately 34 hours after the 2nd dose. I went to my OB for heavy vaginal bleeding with an ultrasound completed 49 hours post vaccine with no concerns visually. Estimated miscarriage <72 hours after vaccine administration with confirmation via ultrasound 1 week and 2 days after vaccine.


VAERS ID: 1096648 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-01-26
Onset:2021-01-26
   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 - / 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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: vsafe

Write-up: After my second dose Pfizer vaccine, on the day or day after I suffered a miscarriage.


VAERS ID: 1104476 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-01-09
Onset:2021-01-26
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-03-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Sertraline 200mg daily Trazodone 25mg nightly Prenatal vitamin
Current Illness: None
Preexisting Conditions: Depression/Anxiety Recurrent miscarriages
Allergies: No known allergies
Diagnostic Lab Data: Genetic testing of embryo showed trisomy 12.
CDC Split Type:

Write-up: Miscarriage: LMP 11/17/20, diagnosis of MAB on 1/26/21. Chromosomal testing of the embryo determined cause of miscarriage to be trisomy 12. Prior to this most recent miscarriage I had 3 previous miscarriages and 1 live birth (1 living child). To be clear, I do not blame the vaccine for the miscarriage, the chromosomes of the embryo were determined before I got my first Covid vaccine.


VAERS ID: 1162303 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-12
Onset:2021-01-26
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-04-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 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? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Pregnancy (Patient no longer pregnant at the time of reporting.)
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage; Pregnancy
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021306867

Write-up: Miscarriage; This is a spontaneous report from a contactable other healthcare professional. This is a report received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202103201227517560, Safety Report Unique Identifier GB-MHRA-ADR 24984382. A 34-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 12Jan2021 at single dose for COVID-19 immunization. Medical history included miscarriage, pregnancy, ongoing pregnancy: Patient no longer pregnant at the time of reporting. The patient became pregnant while taking BNT162B2. Patient last menstrual period date: 27Nov2020. The patient was pregnant again. Patient had not had symptoms associated with COVID-19. Not had a COVID-19 test. Patient was not enrolled in clinical trial. Patient was not currently breastfeeding. The patient''s concomitant medications were not reported. The patient experienced maternal exposure during pregnancy on an unspecified date, miscarriage on 26Jan2021. Events were reported as medical significant. Unaware of pregnancy when receiving 1st vaccine, had a miscarriage two weeks after 1st vaccine. It was unsure if the medicine had an adverse effect on any aspect of the pregnancy, patient was pregnant again and concerned regarding having second vaccine. Patient was exposed to the medicine first-trimester (1-12 weeks). Unaware of pregnancy, misscarage 2 weeks after vaccine. Patient had not tested positive for COVID-19 since having the vaccine. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 981097 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: New York  
Vaccinated:2021-01-25
Onset:2021-01-27
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-01-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029L20A / 2 RA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025J20A / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Injection site erythema, Injection site induration, Injection site pruritus, Injection site swelling, Injection site warmth, Pregnancy, Skin hyperpigmentation, Ultrasound abdomen
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: wellbutrin Adderall xr
Current Illness:
Preexisting Conditions: none
Allergies: NKA
Diagnostic Lab Data: Abd Ultrasound 1/23/21
CDC Split Type:

Write-up: A large area around my injection site was red, swollen, warm to touch, firm and itchy covering 3/4 of my upper arm into my underarm and lymph nodes. I received my first vaccine on 12/23/20 several days after injection the site became very itchy, red and swollen but in a much smaller area and persisted for several days leaving a small area of skin hyper pigmented for ~2 weeks. However I did not think it was considered an "Adverse" event and would have not reported it if the second dose was to a similar scale. Also, when I received first vaccine I did not know I was pregnant at the time. When I went to the doctor on 1/23/21 I was told I was 7.5 weeks pregnant, but there was no heart beat and I had miscarried. Being that I am over the age of 40 and a high risk for pregnancy and miscarriage I am unsure if my miscarriage is directly related to the vaccine but I felt it should add it to the report. My first vaccine was administered on 12/23/20 @ 5:30pm at Hospital


VAERS ID: 981111 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: New York  
Vaccinated:2021-01-25
Onset:2021-01-27
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-01-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025J20A / 1 RA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029L20A / UNK RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Erythema, Feeling hot, Induration, Injection site mass, Injection site pruritus, Injection site swelling, Lymphadenopathy, Peripheral swelling, Pregnancy, Pruritus, Skin hyperpigmentation, Tenderness, Ultrasound abdomen
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Aderall xr wellbutrin
Current Illness: none
Preexisting Conditions: none
Allergies: nka
Diagnostic Lab Data: Abd ultra sound 1/23/21
CDC Split Type:

Write-up: My second dose was on 1/25/21 . One day after my 3/4 of my upper arm into my axillary area became red, swollen, warm to touch, tender to touch, firm and itchy. My axillary lymph nodes were also swollen and tender to touch. My first vaccine was on 12/23/20. Several days after a small area around the injection site became swollen and itchy. I also had a small palpable lump under my skin at the injection and my skin had a small area of hyper pigmentation for ~2 weeks. Again the area was much smaller and I did not think it would be considered an "Adverse" effect. I was also unaware that I was several weeks pregnant at the time of my first vaccine. when I went to the doctors office on 1/23/21 I was told I was 7.5 weeks pregnant, there was no heartbeat and I had miscarried.


VAERS ID: 1022165 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-01-21
Onset:2021-01-27
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-02-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 027/L20A / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion induced, 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? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: PRENATAL VITAMINS, PROGESTERONE PESSARIES, ADDERALL, ASPIRIN
Current Illness: ANXIETY / DEPRESSION
Preexisting Conditions: ADD, ANXIETY, MIGRAINES,EXRECISE INDUCED ASTHMA CERVICAL DISC DEGENERATION.
Allergies: MONOCYCLINE
Diagnostic Lab Data: NONE
CDC Split Type:

Write-up: PATIENT HAD A MISSED ABORTION, FOUND OUT 6DAYS AFTER VACCINATION. HAD HISTORY OF PREVIOUS MISCARRIAGES. WAS ON PROGESTERONE PESSARIES AND ASPIRIN. FETAL HEART BEAT MISSING ON ROUTINE REVIEW. GESTATION 10WEEKS+4DAYS. REQUIRED MEDICAL TERMINATION OF PREGNANCY.


VAERS ID: 1054987 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Maryland  
Vaccinated:2021-01-20
Onset:2021-01-27
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-02-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ1686 / 2 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound scan, 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? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vit
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Ultrasound with low heart rate of fetus. Hcg levels decline from Wednesday 26-friday 29 from 5,400 to 1,500.
CDC Split Type:

Write-up: Pregnancy history: 1 previous pregnancy with healthy full term vaginal delivery. No complications. Estimated due date: Sept, 23, 2021. Symptoms: vaginal bleeding starting Jan 26th. Progressing to miscarriage on 1/29/21


VAERS ID: 1216055 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-06
Onset:2021-01-27
   Days after vaccination:21
Submitted: 0000-00-00
Entered: 2021-04-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / SYR

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Body temperature increased, Exposure during pregnancy
SMQs:, Neuroleptic malignant syndrome (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? Yes
Birth Defect? Yes
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: None.
Current Illness: Asthma
Preexisting Conditions: Asthma
Allergies: Penicillin
Diagnostic Lab Data: The fetus tested positive for Trisomy 15 and Trisomy 21. Trisomy 15 I was told is extremely rare and it is very odd to have both Trisomy 15 and 21. The baby stopped growing at 6 weeks and 3 days. At which point I had to attend multiple ultrasounds to ensure the fetus did not have a heartbeat. After 3 weeks of testing I had to have the fetus surgically removed because my body was not recognizing that the fetus was no longer living and was not rejecting it.
CDC Split Type:

Write-up: I received the vaccine and was unknowingly pregnant. My first shot was on 1/6/2021 and my second shot was on 1/27/2021. I conceived on 1/25/2021. I ended up miscarrying the child and when they sent it in for testing it had 2 abnormal chromosomes. One of which they said is very rare and they have no idea how or why the baby had this. I was told that the vaccine was supposed to be safe for pregnant people but with no family history of anything like this happening and no history of any children being born with mutations I believe this happened from the vaccine. Possibly caused by the spike in temperature I experienced after the second shot. I should have been due to deliver 10/2021.


VAERS ID: 1646553 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Arizona  
Vaccinated:2021-01-12
Onset:2021-01-27
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-08-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0142 / 2 LA / -

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Menstruation irregular, SARS-CoV-2 test
SMQs:, Termination of pregnancy and risk of abortion (narrow), Fertility disorders (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? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Hypothyroidism; Latex allergy (known allergies: latex, hydrocodone)
Allergies:
Diagnostic Lab Data: Test Name: Nasal Swab; Test Result: Negative
CDC Split Type: USPFIZER INC202101007192

Write-up: miscarriage; irregular menstrual cycle; This is a spontaneous report from a contactable nurse (patient). A 37-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration, administered in the left arm on 12Jan2021 (Batch/Lot Number: El0142) as dose 2, single (at the age of 37-years-old) for Covid-19 immunisation. Medical history included hypothyroidism and known allergies to latex and Hydrocodone. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medication included a compounded thyroid medication. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration, administered in the left arm on 22Dec2020 (Batch/Lot Number: Eh9899) as dose 1, single (at the age of 37-years-old) for Covid-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced irregular menstrual cycle and miscarriage on 27Jan2021. The patient underwent lab tests and procedures which included nasal swab with a negative result on an unknown date. No treatment was administered for the events. The outcome of the events was unknown. The events resulted in doctor or other healthcare professional office/clinic visit.; Sender''s Comments: Based on temporal association and known safety profile of the product, a contribution from the suspect drug bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), to the reported event abortion spontaneous cannot be completely 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: 1181238 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-27
Onset:2021-01-27
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 300042698 / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion missed, 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: Medical History/Concurrent Conditions: Disease risk factor
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLMODERNATX, INC.MOD20210

Write-up: Missed abortion; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 31-Mar-2021 and was forwarded to Moderna on 31-Mar-2021. This regulatory authority pregnancy case was reported by a consumer and describes the occurrence of ABORTION MISSED (Missed abortion) in a 30-year-old female patient who received mRNA-1273 (COVID 19 Vaccine Moderna) (batch no. 300042698) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included Disease risk factor. On 27-Jan-2021, the patient received first dose of mRNA-1273 (COVID 19 Vaccine Moderna) (unknown route) 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 27-Jan-2021, the patient experienced MATERNAL EXPOSURE DURING PREGNANCY. On 18-Mar-2021, the patient experienced ABORTION MISSED (Missed abortion) (seriousness criterion medically significant). On 27-Jan-2021, MATERNAL EXPOSURE DURING PREGNANCY had resolved. At the time of the report, ABORTION MISSED (Missed abortion) outcome was unknown. The action taken with mRNA-1273 (COVID 19 Vaccine Moderna) (Unknown Route) was unknown. No concomitant medication provided. No treatment information was provided. This is a case of product exposure during pregnancy (unknown gestational age) with missed abortion for this 30-year-old female. Very limited information regarding this events has been provided at this time. No follow up is possible. Reporter did not allow further contact; Sender''s Comments: This is a case of product exposure during pregnancy (unknown gestational age) with missed abortion for this 30-year-old female. Very limited information regarding this events has been provided at this time. No follow up is possible.


VAERS ID: 1284505 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-27
Onset:2021-01-27
   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 EJ6797 / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Arthralgia, Body temperature, Headache, Myalgia, Pyrexia
SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Eosinophilic pneumonia (broad), Termination of pregnancy and risk of abortion (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NAUSEFE; FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Euthyroid goiter; Obesity; Termination of pregnancy - elective; Vacuum extractor delivery
Allergies:
Diagnostic Lab Data: Test Date: 20210127; Test Name: Body temperature; Result Unstructured Data: Test Result:38.2 Centigrade
CDC Split Type: PTPFIZER INC2021431110

Write-up: spontaneous abortion in unknown pregnancy when performing the 2nd dose of COMINARTY vaccine; Arthralgias; Myalgias; Headaches; Subfebrile (maximum 38.2 tympanic); This is a spontaneous report from a contactable physician (patient) downloaded from the Regulatory Authority PT-INFARMED-T202103-2915. A 33-years-old female patient (pregnant at time of vaccination, 10 weeks of gestation period) received the second dose of BNT162B2 (COMIRNATY), via intramuscular on 27Jan2021 (Lot number: EJ6797) at 0.3 mL, single for COVID-19 immunisation. Medical history included euthyroid goiter and unknown if ongoing that was colloid goiter, but euthyroid; vacuum extractor delivery from 2018 and unknown if ongoing; termination of pregnancy-elective from 2016 and unknown if ongoing; obesity and unknown if ongoing. Obstetric history of voluntary termination of pregnancy in 2016 at 7 weeks; evolutionary pregnancy without complications with term delivery, by suction cup in May2018. There is no known history of spontaneous abortion prior to the reported situation. Concomitant medications included dicycloverine hydrochloride, doxylamine succinate, pyridoxine hydrochloride (NAUSEFE); folic acid and unspecified drug. The patient previously took clavulanic acid that experienced transaminases increased and (palmar) rash desquamating; and received the first dose of BNT162B2 (COMIRNATY), via intramuscular on 06Jan2021 (at the age of 33 years old) (Lot number: EJ6797) at 0.3 mL, single for COVID-19 immunisation. The patient was not previously infected with the SARS-CoV-2 virus. On 27Jan2021, the patient had adverse reaction (ADR) included "Subfebrile (maximum 38.2 tympanic), headache, myalgia and arthralgia" appeared on the very day on which the second dose of the suspected drug was administered, lasting 72 hours. The ADR "spontaneous abortion in unknown pregnancy when performing the 2nd dose of COMINARTY vaccine" was detected 55 days after the second dose of vaccine. The suspicious drug was not suspended since the vaccination schedule was already complete with the administration of the 2 predicted doses. There was no suspicion of interaction between drugs. Uterine emptying was performed with aspiration / curettage after vaginal application of misoprostol on the day of detection of missed abortion. It was reported that the conception will have occurred on the 15th or 16th of January 2021 and the date of the diagnosis of the retained abortion was 23Mar2021, in which it would have 11 weeks and 3 days by ultrasound dating and the embryo had a craniocaudal length compatible with 10 weeks, that was, the abortion had occurred a week and a few days before the diagnosis on 23Mar2021. All events with the medically significant. Lab data include patient body temperature was 38.2 centigrade on 27Jan2021. Specific treatment of the reaction was carried out, "subfebrile (maximum 38.2 tympanic), headache, myalgia and arthralgia", with Ibuprofen 600 mg and Paracetamol 1000 mg. The outcome of the event abortion spontaneous was resolved with sequel on unspecified date, while of the other events was recovered on 30Jan2021. Reporter comment: Concomitant Medication-No. Did Medication Error Occur? - No. Other information-The case reported is about myself. I carried out COMINARTY vaccine on 6Jan and 27Jan2021. Pregnancy diagnosis on 29Jan2021. Spontaneous abortion at 10 weeks (by craneocaudal embryo length) diagnosed on 23Mar2021. There may be no relationship with the vaccine but given the lack of data, I report. No follow-up attempts needed. No further information expected.


VAERS ID: 1830310 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2021-01-27
Onset:2021-01-27
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-10-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ 6136 / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Foetal death, Foetal growth restriction, Foetal heart rate, Foetal heart rate abnormal, Maternal exposure during pregnancy
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? Yes
   Date died: 2021-09-23
   Days after onset: 238
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: heart beat; Result Unstructured Data: Test Result:cessation of beating; Comments: cessation of beating of the child''s heart
CDC Split Type: HRPFIZER INC202101444072

Write-up: cessation of beating of the child''s heart; growth delay; cessation of the beating of the child''s heart and growth delay/ patient died; The mother was on the first trimester of pregnancy; This is a spontaneous report from a contactable consumer (parent- mother). This consumer reported information for herself and her child. This is the fetus report. The maternal report is based on report downloaded from the regulatory authority ; the Regulatory Authority report number is HR-HALMED-300051238. A fetus patient of an unspecified gender received the second dose of BNT162B2 (COMIRNATY), transplacental on 27Jan2021 (batch/lot number: EJ 6136) as DOSE 2, 0.3 mL SINGLE for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. The mother was on the first trimester of pregnancy (reported as 11 weeks gestation). On an unspecified date, the patient experienced foetal heartbeat absent and foetal growth retardation. The mother reported cessation of beating of the child''s heart and growth delay. The patient died (fetal death) on 23Sep2021. It was not reported if an autopsy was performed. Result of Assessment: Comirnaty/ event(s):/ HALMED: Unlikely No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : HR-PFIZER INC-202101435310 maternal case; Reported Cause(s) of Death: Fetal death; Foetal heartbeat absent; Foetal growth retardation


VAERS ID: 1057557 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-01-28
Onset:2021-01-28
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-02-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / -

Administered by: Private       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? 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: USPFIZER INC2021148323

Write-up: Miscarriage 8 days after receiving 2nd vaccine at 6 weeks pregnant; receiving 2nd vaccine at 6 weeks pregnant; receiving 2nd vaccine at 6 weeks pregnant; This is a spontaneous report from a contactable other healthcare professional (patient). A 31-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), lot/batch number not reported, via an unspecified route of administration in the left arm on 28Jan2021 08:30 at a single dose for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) in the left arm on 07Jan2021 at 09:00 AM for COVID-19 immunization. Patient was pregnant. Patient has no other vaccines in four weeks and no other medications in two weeks. Patient has no COVID prior vaccination and no known allergies. On 05Feb2021 at 06:00 PM, patient experienced miscarriage 8 days after receiving 2nd vaccine at 6 weeks pregnant. No treatment received for the event miscarriage. The event resulted in doctor''s office/clinic visit. The patient was not tested for COVID post vaccination. The outcome of the event miscarriage was recovering. Information on the lot/ batch number has been requested.; Sender''s Comments: Based on the compatible temporal association, a possible contributory role of the vaccination with BNT162B2 in triggering the onset of miscarriage in this patient at 6 weeks pregnant cannot be excluded. Additional information regarding relevant medical history, concomitant medications and detailed clinical course around the event onset will aid in comprehensive assessment of the case. 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: 1664949 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-28
Onset:2021-01-28
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-09-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6795 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Maternal exposure before pregnancy, Maternal exposure during pregnancy, SARS-CoV-2 test positive, 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), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: COVID-19; Disease risk factor
Allergies:
Diagnostic Lab Data: Test Name: blood test; Result Unstructured Data: Test Result:results unavailable; Test Date: 20201109; Test Name: COVID-19; Test Result: Positive ; Comments: corona, confirmed by test; Test Name: transvaginal ultrasound; Result Unstructured Data: Test Result:fetus with heartbeat; Comments: 7th week; Test Name: transvaginal ultrasound; Result Unstructured Data: Test Result:fetus without heartbeat; Comments: 11th week
CDC Split Type: NLPFIZER INC202101073364

Write-up: Miscarriage; Maternal exposure during pregnancy; The second vaccination took place before pregnancy.; This is a spontaneous report from a contactable consumer or other non hcp downloaded from the regulatory authority-WEB, regulatory authority number NL-LRB-00667042. A 31-years-old non pregnant female patient received second dose of BNT162B2 (COMIRNATY, Formulation: Solution for injection, Batch/lot number: EJ6795) via an unspecified route of administration on 28Jan2021 as single dose for covid-19 immunisation. Medical history included covid-19 from 09Nov2020 to an unknown date, disease risk factor from an unknown date and unknown if ongoing. Concomitant medication(s) included folic acid (FOLIC ACID) taken for an unspecified indication, start and stop date were not reported. The patient had historical vaccine of BNT162B2 (COMIRNATY, formulation: Solution for injection, Batch/lot number was not reported) via an unspecified route of administration on 07Jan2021 as single dose for covid-19 immunisation. On 09Aug2021 the patient experienced miscarriage, maternal exposure during pregnancy, the second vaccination took place before pregnancy. The patient underwent lab tests and procedures which included blood test results unavailable on unspecified date, sars-cov-2 test positive: positive on 09Nov2020 corona, confirmed by test, ultrasound scan vagina: fetus with heartbeat on unspecified date 7th week, ultrasound scan vagina: fetus without heartbeat on unspecified date 11th week. The clinical outcome of the events was unknown. Sender Comment: Seriousness of miscarriage was changed from "death and congenital anomaly" to "other medically important condition". No follow-up attempts possible. No further information expected.; Reporter''s Comments: BioNTech/Pfizer vaccine (Comirnaty) Past drug therapy BioNTech/Pfizer vaccin (Comirnaty): yes ADRs: Miscarriage Date: 07Jan2021 miscarriage - reaction: vitality ultrasound at 7 weeks with heartbeat, at 11 weeks no longer any heartbeat, presumably stopped growing around 9 weeks COVID19 - Previous COVID-19 infection: disease symptoms: little Other - diagnostic procedures: transvaginal ultrasound, blood test


VAERS ID: 1020877 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-01-29
Onset:2021-01-29
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9265 / 1 LA / IM

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

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

Write-up: I was a healthy pregnant woman age 43 who was 11 weeks 2 days pregnant. I was having a normal pregnancy with no complications. I''m in healthcare and in the operating often for airway and ENT procedures. I received my shot at 9:00am on 1/29/20201 and began spotting at 11:00am. The spotting continued (very light) until 9:00pm. I decided to go to bed since I wasn''t feeling well. I woke at 2:00am with contractions and heavy bleeding. I went to the ED at 3:00am on 1/30 to confirm my miscarriage. I weighed 121 at the ED when triaged. My EDD was 08/19/2021


VAERS ID: 1036567 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-01-27
Onset:2021-01-29
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-02-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 028L20A / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Chills, Exposure during pregnancy, Foetal death, Headache, Nausea, Pyrexia, Ultrasound foetal abnormal
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (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), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Pre-natal vitamin and Bonjesta
Current Illness: Reports only morning sickness, related to pregnancy.
Preexisting Conditions: Denies
Allergies: NKDA, NKA
Diagnostic Lab Data: 2/1/21 Fetal US reported as showed fetal demise during week 8, which is the same week as she received the #2 COVID vaccine
CDC Split Type:

Write-up: reports that she was approximately 8 weeks pregnant at the time of her #2 COVID vaccine on 1/27/21. She reports she had a normal prenatal US at 7 weeks. She reports on 1/27/21, she had vaccine side effects of fever/chills, headache, and nausea. She notes on 1/29/21 most of her vaccine side effect symptoms resolved, but she is still suffering from headaches. She also notes that her morning sickness was gone on 1/29/21. She reports she called her OB, he brought her in for a repeat US on 2/1/21. Notes that she has two healthy children and suffered a miscarriage in May 2020.


VAERS ID: 1044638 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-01-28
Onset:2021-01-29
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-02-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA NA / 1 LA / SYR

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Injected limb mobility decreased, Injection site mass, Pain, Rash
SMQs:, Anaphylactic reaction (broad), Extravasation events (injections, infusions and implants) (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? 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: Golf ball size lump on my arm at injection site that lasted 3 weeks and didn''t reduce in size. Inability to use arm without extreme pain. Rash that felt like a burn on arm 12 weeks pregnant at the time of injection Pregnancy was lost


VAERS ID: 1104214 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-01-09
Onset:2021-01-29
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-03-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011J20A / 1 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abortion induced, Cytogenetic abnormality, Exposure during pregnancy, Fatigue, Genetic counselling, Human chorionic gonadotropin normal, Injection site pain, Laboratory test normal, Occupational exposure to SARS-CoV-2, Ultrasound antenatal screen abnormal, Uterine dilation and evacuation
SMQs:, Congenital, familial and genetic disorders (narrow), Extravasation events (injections, infusions and implants) (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), COVID-19 (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Acyclovir 400mg 1x/day, Ritual essential prenatal vitamin 2 capsules/day, and Folic acid 3mg 1x/day.
Current Illness: None.
Preexisting Conditions: Cold sores, headaches/migraines
Allergies: Flagyl- fever and diarrhea. Bee stings - toxic reaction (no anaphylaxis).
Diagnostic Lab Data: Ultrasound 1/29/2021: increased nuchal translucency of 3.55mm, absent nasal bone, fluid around fetus?s abdomen. Abnormalities concerning for chromosomal/genetic condition. Panorama and Horizon 274 maternal carrier screenings 1/29/2021: normal without increased risk identified for any of the chromosomal/genetic conditions tested Ultrasound 2/2/2021: increased nuchal translucency now 4.3mm, and also found the presence of a cystic hygroma. Abnormalities concerning for chromosomal/genetic condition not yet tested. Chorionic villus sampling 2/2/2021: all results normal without concern for any of the chromosomal or genetic conditions tested. Ultrasound 2/19/2021: the fetus?s humerus measured in the 1st percentile for gestational age and the fetus?s femur measured in the 3rd percentile for gestational age. Dilation and evacuation 2/24/21: awaiting results of pathology report from procedure. Exome testing 2/24/21: awaiting results of testing, can take 2-3 months to receive.
CDC Split Type:

Write-up: I was 9 weeks and 2 days pregnant with my first pregnancy (no history of miscarriages) when I received my first dose of the Moderna vaccine on 1/9/2021. I had a routine appointment with my OB-GYN the day prior, 1/8/2021, during which they completed a routine ultrasound. At that time, the ultra sound was completely normal with a healthy fetus and heart rate, and my due date was estimated to be 8/13/2021. Also at that time, I was advised by my OB-GYN to get the COVID vaccine, when offered to me, given my higher risk of contracting COVID due to my job as a healthcare worker with direct patient contact, and my higher risk for more severe illness if I contracted COVID due to pregnancy. I received the vaccine the next day with no immediate adverse reactions/events aside from some considerable arm soreness at the site of the vaccine and fatigue. Then 2 weeks and 6 days later I had another routine appointment with my OB-GYN (1/29/2021) at which point in time I was 12 weeks and 1 day pregnant. During this visit they conducted a second routine ultrasound. From this ultra sound they identified multiple abnormalities including an increased nuchal translucency of 3.5 mm, absent nasal bone, and presence of fluid around the fetus?s abdomen. These abnormalities were concerning for a chromosomal/genetic abnormality. Given these concerns I had labs drawn for maternal carrier screening (the Panorama and the Horizon 274), and I was referred to maternal fetal medicine for further imaging and testing. The results of the lab work took approximately 2 weeks to receive, but they came back normal without increased risk identified for any of the chromosomal/genetic conditions tested. I was seen by a high risk doctor and a genetic counselor within the maternal fetal medicine department on 2/2/2021. At this appointment I had a third ultrasound completed which confirmed the presence of an increased nuchal translucency now 4.3mm, and also found the presence of a cystic hygroma. These findings were again consistent with concerns for a chromosomal, genetic or other anatomical/structural condition and as such I had a chorionic villus sampling done that same day to assess the DNA of the fetus. These results also came back all normal without concern for any of the chromosomal or genetic conditions tested. I then had a follow up appointment and ultrasound with the maternal fetal medicine department on 2/19/2021, at which point I was 15 weeks and 1 day pregnant. This early anatomical scan revealed even more concerning findings with the fetus?s humerus measuring in the 1st percentile for gestational age and the fetus?s femur measuring in the 3rd percentile for gestational age. Per consultation with our genetic counselor this was indicative or some severe condition; however, it was not clear exactly what condition. Given the severity of the findings it was recommended to terminate the pregnancy. As such I had to undergo a dilation and evacuation procedure on 2/24/2021. We are currently still awaiting results of further genetic testing (exome testing), the results of which can take 2-3 months from the time of sending out the labs (sent out around 2/24/2021).


VAERS ID: 1107257 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-01-29
Onset:2021-01-29
   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 - / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021223221

Write-up: Miscarriage; Pregnant at time of vacciation; Pregnant at time of vacciation; This is a spontaneous report from a non-contactable consumer. A 34-year-old female patient (16 weeks pregnant at time of vaccination) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on 29Jan2021 (at the age of 34-years-old) as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient experienced miscarriage at a routine OBGYN visit on 19Feb2021. The patient was hospitalized for the miscarriage on an unknown date for 2 days. The clinical outcome of the event miscarriage was unknown. The patient had not had COVID prior to the vaccination and has not tested positive post vaccination. Information about lot/batch has been requested.


VAERS ID: 1065042 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-09
Onset:2021-01-29
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 1 - / -

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

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: Pregnancy
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 2021; Test Name: Ultrasound; Result Unstructured Data: Test Result:unknown result
CDC Split Type: NLPFIZER INC2021169340

Write-up: I got the vaccine. I didn''t know then that I was pregnant.; miscarriage at 6 weeks of pregnancy; pain; This is a spontaneous report from a contactable consumer (patient) downloaded from the regulatory authority-WEB NL-LRB-00437911 A 33-years-old female patient received first dose of bnt162b2 (COMIRNATY), via an unspecified route of administration on 09Jan2021 at SINGLE DOSE for covid-19 immunisation. Medical history included ongoing pregnancy. The patient''s concomitant medications were not reported. The patient experienced miscarriage at 6 weeks of pregnancy on 29Jan2021 with outcome of recovering, which is medically significant, pain (vaccination site pain) in 2021 and i got the vaccine. i didn''t know then that i was pregnant on an unspecified date with outcome of unknown. The mother reported she became pregnant while taking bnt162b2. The mother was 6 Weeks pregnant at the onset of the event. The pregnancy resulted in spontaneous abortion. Case narrative provided as: This serious spontaneous report from a consumer concerns a female aged 33 years, with miscarriage (other medically important condition) and injection site pain, following administration of covid-19 vaccin pfizer injection fliud (action taken: not applicable) for covid 19 immunisation. The patient was unaware of her pregnancy at the time of vaccination, which occurred at approximately gestational age 3 weeks. The miscarriage occurred at gestational age 6 weeks. Lab data included Ultrasound in 2021 unknown result. Case Summary and Reporter''s Comments Text: Pfizer vaccine (Comirnaty) miscarriage at 6 weeks of pregnancy. Additional information ADR: On 09Jan2021 I received the vaccine. I didn''t know then that I was pregnant. On 20Jan2021 I found out that I was pregnant. But this unfortunately ended in a miscarriage on 29Jan2021. It could of course be a coincidence, but I still want to report this. I did not have the second vaccine because I was pregnant. confounding factors COVID-19 vaccine exposure during pregnancy week: approximately one week after conception, already calculating back. COVID19:Previous COVID-19 infection: No. Other diagnostic procedures: Ultrasound after miscarriage No follow-up attempts possible, no further information expected. Information about lot/batch# cannot be obtain.


VAERS ID: 1107048 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-27
Onset:2021-01-29
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-03-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6136 / 2 RA / OT

Administered by: Other       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? 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: 20210129; Test Name: Blood human chorionic gonadotrophin negative; Test Result: Negative
CDC Split Type: ITPFIZER INC2021222017

Write-up: Abortion spontaneous; This is as spontaneous report from a contactable other health professional via health authority downloaded from the Regulatory Authority-WEB. The regulatory authority report number is IT-MINISAL02-681597. A 31-year-old female patient received the second dose of bnt162b2 (COMIRNATY;lot EJ6136; expiration 30Apr2021) intramuscular in right arm on 27Jan2021 at 11:15 at single dose for covid-19 vaccination. The patient medical history and concomitant medications were not reported. Patient took first dose of the vaccine (Lot: EL1484 exp. 30Apr2021) on 06Jan2021 at 11:10 in right arm and experienced adverse reaction. The patient experienced abortion spontaneous on 29Jan2021.The patient became pregnant while taking bnt162b2; she was 6 weeks pregnant at the onset of the event. The fetal outcome is intrauterine death. Blood human chorionic gonadotrophin was negative on 29Jan2021. Outcome of the event was reported as recovered in 2021. Sender''s Comment: Previous suspected adverse reaction from first dose of Comirnaty vaccine. Reported with reference number 651811.No follow-up attempts possible. No further information expected.


VAERS ID: 1339967 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-29
Onset:2021-01-29
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6134 / 1 - / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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: Test Name: ultrasound; Result Unstructured Data: Test Result:Unknown results
CDC Split Type: PTPFIZER INC2021512301

Write-up: At the 1st dose of the vaccine was already pregnant but was not aware of it. Had the vaccine on 29Jan, found out that was pregnant on 10Feb and the pregnancy ended by placental detachment on 10Mar; At the 1st dose of the vaccine was already pregnant but was not aware of it. Had the vaccine on 29Jan, found out that was pregnant on 10Feb; This is a spontaneous report from a contactable other healthcare professional (patient) downloaded from the Regulatory Authority-WEB, regulatory authority number PT-INFARMED-R202104-3304. A 35-year-old female pregnant patient received bnt162b2 (COMIRNATY, solution for injection), intramuscular on 29Jan2021 (batch/lot number EJ6134 and expiry date unknown) at 35 years of age as 1st dose, 0.3 ml single for covid-19 immunization. The patient''s medical history and concomitant medications were not reported. The patient previously took minigeste. The patient experienced at the 1st dose of the vaccine was already pregnant but was not aware of it. had the vaccine on 29jan, found out that was pregnant on 10feb and the pregnancy ended by placental detachment on 10mar. The patient presented termination of pregnancy by placental detachment on 10Mar2021 (40 days after the administration of the suspect medication), associated with the use of Comirnaty, mRNA vaccine against COVID-19 (with modified nucleoside), SARS-CoV-2 Virus, Spike (S) protein, mRNA, BNT162b2 - 0.5 mg/ml, lot EJ6134 on first use on 29Jan2021. The ADR caused hospitalization with ultrasound and curettage on 14Mar2021. The outcome of the event "abortion" was recovered on 10Mar2021. No follow-up attempts are needed. No further information is expected.


VAERS ID: 1381624 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-29
Onset:2021-01-29
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC2021590724

Write-up: Bleeding premature abortion; she became pregnant while taking bnt162b2; This is a spontaneous report from a non-contactable consumer WEB, regulatory authority number DE-PEI-CADR2021016736, Safety Report Unique Identifier DE-PEI-2021007257. A 32-years-old female patient received bnt162b2 (COMIRNATY), dose 1 intramuscular on 29Jan2021 at age of 32-years-old as 1st dose, 0.3 ml single dose for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient experienced bleeding premature abortion on 07Feb2021. The mother reported she became pregnant while taking bnt162b2. The mother was 1 Months pregnant at the onset of the event. The outcome of the event was unknown. Senders comments: Information on risk factors or previous illnesses none / fertilization / ovulation on 27 / 28Jan vaccination on 29Jan Bleeding since 07Feb persistent. No follow-up attempts are possible, information on batch number cannot be obtained.


VAERS ID: 1456007 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-29
Onset:2021-01-29
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6136 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Dizziness, Influenza like illness, Nausea
SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (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? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: IEPFIZER INC2021752714

Write-up: MISCARRIAGE; NAUSEA; FLU SYMPTOMS; DIZZINESS; This is a spontaneous report from a contactable other healthcare professional downloaded from the Agency Regulatory Authority-WEB. The regulatory authority report number is IE-HPRA-2021-071659. A 36-year-old female patient received the second dose of BNT162B2 (COMIRNATY, lot number EJ6136), via an unspecified route of administration on 29Jan2021 as dose 2, single for covid-19 immunisation. The patient has no relevant medical history/underlying conditions. Historical vaccine included the first dose of BNT162B2 (COMIRNATY, lot number EJ6795) on 08Jan2021 for covid-19 immunisation. The patient''s concomitant medications were not reported. The patient experienced miscarriage (medically significant) on 14Feb2021 with outcome of recovered on an unspecified date in 2021; and nausea, flu symptoms and, dizziness on 29Jan2021 with outcomes of recovered on 05Feb2021. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1855646 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-28
Onset:2021-01-29
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6136 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Body temperature, Body temperature increased, Lymphadenitis, Malaise, Scan
SMQs:, Neuroleptic malignant syndrome (broad), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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: 20210129; Test Name: Body temperature; Result Unstructured Data: Test Result:37.8 degrees Celsius; Test Date: 202102; Test Name: Scan; Result Unstructured Data: Test Result:Control scan: not completely rejected abortion
CDC Split Type: DKPFIZER INC202101455550

Write-up: Spontaneous abortion; General malaise / Feeling ill; Severe lymphadenitis in the armpit of the vaccinated arm.; Body temperature increased to 37.8 degrees Celsius; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority-WEB, regulatory authority number DK-DKMA-WBS-0047296 and Safety Report Unique Identifier DK-DKMA-ADR 24871850. A 32-years-old female patient received bnt162b2 (COMIRNATY, solution for injection, Batch/Lot Number: EJ6136; Expiration Date: 30Apr2021), dose 2 via an unspecified route of administration on 28Jan2021 as dose 2, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient has not reported any other health issues. The patient previously took first dose of bnt162b2 (COMIRNATY, Solution for injection, Lot Number and expiration dates were not reported), via an unspecified route of administration, on 08Jan2021 as for covid-19 immunization. On 29Jan2021, the day after the second vaccination was given, the patient developed General malaise / Feeling ill, Severe lymphadenitis in the armpit of the vaccinated arm and Body temperature increased to 37.8 degrees Celsius. On 03Feb2021, 6 days after the second vaccination was given, the patient developed Spontaneous abortion. As a consequence of the Spontaneous abortion the patient experienced severe pain. The patient had not completely rejected the abortion and therefore had a medical abortion. The patient underwent lab tests and procedures which included body temperature: 37.8 degrees celsius on 29Jan2021, scan: control scan: not completely rejected abortion on Feb2021. The patient did not know that she was pregnant at the time of vaccination. There was a suspicion of pregnancy outside of the uterus. The outcome of Spontaneous abortion was not recovered. The outcome of Body temperature increased to 37.8 degrees Celsius was recovered on 30Jan2021. The outcome of General malaise / Feeling ill was recovered on 31Jan2021. The outcome of Severe lymphadenitis in the armpit of the vaccinated arm was recovered on Feb2021. No follow-up attempts possible. No further information expected.


VAERS ID: 988935 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: South Carolina  
Vaccinated:2021-01-19
Onset:2021-01-30
   Days after vaccination:11
Submitted: 0000-00-00
Entered: 2021-01-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / IM

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

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

Write-up: Became pregnant 12/17/20 and miscarried at gestational age of 6 weeks. Received first vaccine dose on 12/31/20 Received second dose on 1/19/21 Began to miscarry on 1/30/21


VAERS ID: 988939 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-01-28
Onset:2021-01-30
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-01-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK RA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Injection site pain, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Montelukast, 10mg
Current Illness: N/A
Preexisting Conditions: Obesity Asthma
Allergies: Tree nut
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pregnancy confirmed 1/28/2021, 5 weeks 5 days. Pregnancy lost 1/31/2021. Symptoms after Moderna vaccine were low fever and pain at injection site.


VAERS ID: 995325 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-01-06
Onset:2021-01-30
   Days after vaccination:24
Submitted: 0000-00-00
Entered: 2021-02-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 037KLOA / 1 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Back pain, Heavy menstrual bleeding, Human chorionic gonadotropin negative, Muscle spasms, Pregnancy test positive
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), 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? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: none
Preexisting Conditions: Uterine Didelphys - no complication and had previously had one healthy pregnancy and delivery
Allergies: penicillin, sulfa, bees
Diagnostic Lab Data: (2) home pregnancy test on 1-26-21 and 1-27-21 Hcg 3.5 on 2-1-21
CDC Split Type:

Write-up: I took an at-home pregnancy test on 1/26/21 and 1/27/21 after a missed period of which both were positive. On Saturday 1/30/21, I began to have heavy bleeding of which lasted through the weekend. I also experienced cramping and low back pain. On 2/1/21 I had an Hcg lab value of 3.5 confirming I had miscarried. This has lasted through 2/2/21.


VAERS ID: 1058924 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Maryland  
Vaccinated:2021-01-15
Onset:2021-01-30
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-02-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012L20A / 1 LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
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: blood work. normal
CDC Split Type: vsafe

Write-up: Two weeks after the vaccine I had a miscarriage.


VAERS ID: 1065919 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-01-30
Onset:2021-01-30
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / -

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? 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:
CDC Split Type: USPFIZER INC2021143584

Write-up: miscarried; patient was pregnant at the time of the vaccine; patient was pregnant at the time of the vaccine; This is a spontaneous report from a contactable healthcare professional reporting for herself. A 29-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number and expiry date not reported) via an unspecified route of administration at right arm, at the age of 29-year-old, on 30Jan2021 02:00 AM, single dose for COVID-19 immunization. Relevant medical history and concomitant medications were reported as none. The patient had no known allergies. The patient did not receive any other vaccine in four weeks or any other medications in two weeks. The patient was pregnant at the time of the vaccine 30Jan2021 and miscarried on 01Feb2021. LMP was provided as 01Jan2021, gestation period was reported as 4 weeks and due date was provided as 08Oct2021. The patient did not have covid prior vaccination and was not tested for covid post vaccination. The patient did not receive any treatment in response to the event miscarried. Outcome of the event miscarried was not recovered. Information on the lot/batch number has been requested.; Sender''s Comments: Based on the compatible temporal association, a possible contributory role of suspect vaccine BNT162B2 in triggering the misarrange in this 29-year-old pregnant patient cannot be excluded. Additional information regarding relevant medical history, underlying conditions, concomitant medications and detailed clinical course around the event onset will aid in comprehensive assessment of the case. 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: 1703954 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: D.C.  
Vaccinated:2021-01-29
Onset:2021-01-31
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-09-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9261 / 1 LA / IM

Administered by: Military       Purchased by: ?
Symptoms: Abortion spontaneous, Blood thyroid stimulating hormone normal, Fatigue, Feeling cold, Hypothyroidism, Joint stiffness, Musculoskeletal stiffness, Onychoclasis, Tinnitus, Trichorrhexis, Weight increased, Weight loss poor
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Hypothyroidism (narrow), Hearing impairment (narrow), Termination of pregnancy and risk of abortion (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Claritin, probiotics, multivitamin
Current Illness: N/a
Preexisting Conditions: N/a
Allergies: Quinalones, topical iodine
Diagnostic Lab Data: TSH October 2020 2.29 TSH February 24 2021 4.5 TSH June 21 2021 3.4 (5 weeks pregnant)
CDC Split Type:

Write-up: Accelerated progression of hypothyroidism increasing TSH from baseline of 1.8 to 2.3 up to 4.5 in February 2021. Severe symptoms of hypothyroidism including fatigue, coldness, brittle nails and hair, stiff muscles and joints, tinnitus, unexplained weight gain of 8-12 pounds, and difficulty losing weight since. Possible connection between TSH and first trimester miscarriage which took place around 9-11 weeks in late July to early August 2021.


VAERS ID: 995949 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2021-01-22
Onset:2021-02-01
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-02-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3249 / 1 LA / IM

Administered by: Pharmacy       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: Unknown
Current Illness:
Preexisting Conditions:
Allergies: None noted
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage reported


VAERS ID: 1020758 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-01-20
Onset:2021-02-01
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 037K20A / 1 RA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029L20A / 2 RA / IM

Administered by: Work       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? No
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: No
Diagnostic Lab Data: Positive pregnancy test on 1/13/2021 Fetus seen on US with heartbeat on 1/22/21 No heartbeat and no growth on US 2/8/21
CDC Split Type:

Write-up: I was 5 weeks 5 days pregnant with a EDD of 9/17/2021 at the time of my 2?d covid19 vaccine on 1/20/21. On 2/8/21 I found out that my fetus stopped growing at 6w1d, documented on US without heartbeat in the ER. I had a spontaneous miscarriage on 2/9/21.


VAERS ID: 1055663 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-01-29
Onset:2021-02-01
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-02-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Foetal heart rate abnormal, Pregnancy
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), 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 vitamin
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: I was 8-weeks pregnant when I received my first dose of the Pfizer COVID-19 vaccine. This first dose was administered on Friday January 29, 2021. Three days later on Monday February 1, 2021, I was told my baby did not have a heartbeat on the ultrasound in the clinic (confirmed by radiology that day as well) and that I was having a miscarriage. I had no other signs or symptoms of miscarriage or illness. Pregnancy history - I do not have any other children yet.


VAERS ID: 1058751 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-02-01
Onset:2021-02-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-02-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Asthenia, Exposure during pregnancy, Haemorrhage in pregnancy, Pain, Pyrexia, Ultrasound scan, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? Yes
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: No
Current Illness: None
Preexisting Conditions: None
Allergies: No
Diagnostic Lab Data: Ultrasound
CDC Split Type:

Write-up: The evening of my vaccination, I began to feel feverish, weak and achy. During the night I woke with heavy bleeding and found out the following morning I had miscarried my otherwise healthy pregnancy.


VAERS ID: 1071787 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Kentucky  
Vaccinated:2020-12-01
Onset:2021-02-01
   Days after vaccination:62
Submitted: 0000-00-00
Entered: 2021-03-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / 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? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Synthroid, Prozac, vitamin d, vitamin b complex, melatonin, guanfacine, theracurmin, prenatal vitamin, prebiotic, miralax, stool softener, pepcid
Current Illness:
Preexisting Conditions: Hashimotos
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage after 2nd dose given


VAERS ID: 1084690 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-14
Onset:2021-02-01
   Days after vaccination:18
Submitted: 0000-00-00
Entered: 2021-03-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3246 / 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? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Multi-vitamin
Current Illness: no
Preexisting Conditions: no
Allergies: no
Diagnostic Lab Data: Just basic labs - during my pregnancy everything came back normal February 2 - Hospital - After back miscarriage - HCG - that was low but that is to be expected; ultrasound; technically I went to ER but it wasn''t a regular ER visit as my doctor doesn''t take miscarriages in
CDC Split Type: vsafe

Write-up: Miscarried. Due date had been Sept 16, 2021. This was my first pregnancy.


VAERS ID: 1087386 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-01-29
Onset:2021-02-01
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-03-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 042L20A / 2 LA / IM

Administered by: Military       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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Pre natal
Current Illness: None noted
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Patient received the Moderna COVID Vaccine on 29 January, at which time she was 7 weeks pregnant. No other comorbities noted. On 01 February she had a miscarriage. She also received the first dose while pregnant, first dose was given on 30 December 2020 and she was 3 weeks pregnant


VAERS ID: 1087526 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2021-02-04
Onset:2021-02-01
Submitted: 0000-00-00
Entered: 2021-03-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 032L20A / 2 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, 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? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Pre Natal Vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: Sulfa Drugs
Diagnostic Lab Data: Ultrasound. on 03-04-21. DC/DE surgery on 03-09-21.
CDC Split Type:

Write-up: I received my second vaccination in the morning on 02-04-21. I visited my OBGYN that afternoon learned that I was approximately seven weeks pregnant, and that my baby was healthy with a heartbeat, I returned to the OBGYN four weeks later for my routine visit and leaned that the fetus had died around week 8, which was approximately one week after receiving the vaccine. I had no other issues or complications that would have contributed to my miscarriage.


VAERS ID: 1302244 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-01-20
Onset:2021-02-01
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-05-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3249 / 2 RA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Haemorrhage, Human chorionic gonadotropin, Pregnancy test positive, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Tylenol, imitrex, prenatal vitamin, fish oil
Current Illness:
Preexisting Conditions: migraines
Allergies: doxorubicin
Diagnostic Lab Data: miscarriage confirmed via serial HCG testing
CDC Split Type:

Write-up: positive pregnancy test 1/16/21, vaccine 1/20/21, miscarriage with spotting starting @ 6 weeks pregnant on 2/1/21 and additional bleeding 2/2/21-2/7/21.


VAERS ID: 1410114 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Georgia  
Vaccinated:2021-01-20
Onset:2021-02-01
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-06-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 030L20A / 1 LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatals, Metformin for PCOS, Progesterone
Current Illness: None
Preexisting Conditions: PCOS
Allergies: None
Diagnostic Lab Data: D&C Blood work for pregnancy- normal
CDC Split Type: vsafe

Write-up: I had the vaccine on 01/20/2021 and in 03/12/2021 I went to the doctor for my 12 week check up and they said I probably miscarried 2 weeks before. I had a D&C. The delivery date would have been on September 20, other than that I have had a normal pregnancy.


VAERS ID: 1571054 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-01-07
Onset:2021-02-01
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-08-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test abnormal, Pregnancy, Pregnancy test positive, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

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

Write-up: I had my 2nd does of the Pfizer COVID vaccine on Jan 7th. Ovulated and became pregnant on Jan 18th. Started bleeding on Feb 1. I had a positive pregnancy test Friday Feb 5th. Serial blood draws at the doctor the next week confirmed I was pregnant with low chance for a viable pregnancy. Later blood work confirmed I had a miscarriage.


VAERS ID: 1628545 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-02-01
Onset:2021-02-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-08-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK LA / -

Administered by: Military       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: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage


VAERS ID: 1718874 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-02-01
Onset:2021-02-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-09-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029L20A / 2 LA / SYR

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

Write-up: Received my second Covid shot in February, got pregnant shortly after and miscarried at 5 weeks. Can be totally unrelated, miscarriages happen for so many reasons. But just in case there is correlation, I was instructed to file the report


Result pages: prev   1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27   next

New Search

Link To This Search Result:

https://medalerts.org/vaersdb/findfield.php?EVENTS=ON&PAGENO=4&PERPAGE=100&ESORT=ONSET-DATE&SYMPTOMS[]=Aborted_pregnancy_%2810000209%29&SYMPTOMS[]=Abortion_%2810000210%29&SYMPTOMS[]=Abortion_complete_%2810061614%29&SYMPTOMS[]=Abortion_early_%2810052846%29&SYMPTOMS[]=Abortion_incomplete_%2810000217%29&SYMPTOMS[]=Abortion_induced_%2810000220%29&SYMPTOMS[]=Abortion_late_%2810052847%29&SYMPTOMS[]=Abortion_missed_%2810000230%29&SYMPTOMS[]=Abortion_of_ectopic_pregnancy_%2810066266%29&SYMPTOMS[]=Abortion_spontaneous_%2810000234%29&SYMPTOMS[]=Abortion_spontaneous_complete_%2810061616%29&SYMPTOMS[]=Abortion_spontaneous_incomplete_%2810061617%29&SYMPTOMS[]=Foetal_cardiac_arrest_%2810084280%29&SYMPTOMS[]=Foetal_death_%2810055690%29&SYMPTOMS[]=Premature_baby_death_%2810076700%29&SYMPTOMS[]=Premature_delivery_%2810036595%29&SYMPTOMS[]=Stillbirth_%2810042062%29&VAX=COVID19


Copyright © 2021 National Vaccine Information Center. All rights reserved.
21525 Ridgetop Circle, Suite 100, Sterling, VA 20166