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

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

Government Disclaimer on use of this data



Case Details (Sorted by Onset Date)

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VAERS ID: 1628643 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Alabama  
Vaccinated:2021-02-19
Onset:2021-04-16
   Days after vaccination:56
Submitted: 0000-00-00
Entered: 2021-08-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6201 / 2 RA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Flu vaccine; experience flu like symptoms but have not required any medical attention
Other Medications: Lexapro; Flonase spray
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: vsafe

Write-up: I got vaccine back in February 19 2021. I took OTC Tylenol the following day at around 7pm due to the pain I was having. I found out I was pregnant in March 2021. I had a miscarriage on 04-16-2021. I currently am pregnant again and I found out on Father''s Day 06-20-2021. I am currently 14 weeks pregnant as of today. My EDD is 02-22-2022.


VAERS ID: 1438353 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-16
Onset:2021-04-16
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EX2405 / 1 LA / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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: 20210511; Test Name: gynecological consultation; Result Unstructured Data: Test Result:pregnancy stopped at 6 weeks + 4 days; Test Name: blood test; Test Result: Positive ; Comments: pregnancy dating of 4 weeks of gestation period
CDC Split Type: FRPFIZER INC2021704841

Write-up: Early miscarriage; Vaccination against COVID without knowing she was pregnant; This is a spontaneous report downloaded from the WEB. The regulatory authority report number is FR-AFSSAPS-BX20215268 with Safety Report Unique Identifier of FR-AFSSAPS-2021067902. This is a maternal report. A contactable pharmacist reported that a 36-year-old female patient received BNT162B2 (COMIRNATY), via intramuscular route administered in left arm on 16Apr2021 (Batch/Lot Number: EX2405) as dose 1, single for COVID-19 immunisation. The patien''st medical history and concomitant medications were not reported. Date of last menstrual period was not specified. Theoretical start date of pregnancy was 09Apr2021. The patient had no family history mentioned. It was reported that the patient had vaccination against COVID without knowing she was pregnant on 16Apr2021. There was no mention of side effects after and consultation after 4 days with a midwife who performed a blood test revealed positive, pregnancy dating of 4 weeks of gestation period. On 11May2021, day 25 of vaccination, context unknown, gynecological consultation with pregnancy stopped at 6 weeks + 4 days; the patient experienced early miscarriage at 6 weeks of gestation period without further details. The patient has not had Covid-19 and has not been tested. Outcome of event early miscarriage was recovered on an unspecified date. "NB: attribution made without prejudice to the elements of investigations which could be carried out within the framework of legal or amicable compensation procedures." Event occurred in a country different from that of the reporter. This may be a duplicate if the reporter also submitted directly to his/her local agency. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1231961 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-04-16
Onset:2021-04-17
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-04-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Chills, Exposure during pregnancy, Headache, Hyperhidrosis, Pain, Ultrasound scan, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), 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), Hypoglycaemia (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: Progesterone (for pregnancy), Prenatal Vitamins
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: Ultrasounds, BHCG & Progesterone Blood Test
CDC Split Type:

Write-up: I received my second vaccine dose on Friday, 4/16. At the time I was 6 weeks and 4 days pregnant. I woke up at three o''clock in the morning on Saturday, 4/17 sweating with chills, body aches and a headache. When I went to the bathroom at six o''clock AM I noticed that I was bleeding. I called my doctor and she told me to monitor the bleeding over the weekend and to call first thing Monday morning for an ultrasound. I continued bleeding throughout the weekend and yesterday (4/19) my doctor confirmed that I was experience a miscarriage.


VAERS ID: 1239091 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Wyoming  
Vaccinated:2021-04-16
Onset:2021-04-17
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-04-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0151 / 1 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abdominal pain, Abdominal pain upper, Abortion spontaneous, Arthralgia, Blood test, Dizziness, Exposure during pregnancy, Myalgia, Nausea, Ultrasound antenatal screen abnormal, Urine analysis, Vaginal haemorrhage
SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Vestibular disorders (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), Arthritis (broad), Tendinopathies and ligament disorders (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: none
Current Illness: none
Preexisting Conditions: hx cervical medical issues this past year
Allergies: none
Diagnostic Lab Data: U/S, blood work, urine test
CDC Split Type:

Write-up: 04/21/2021- ct 6-7 wks preg when rec''vd 1st dose Pfizer on 04/16/21, c/o ''little'' stomach ache/ dizzy/myalgia that night. 04/17/21-8:30am , vag blding/''little'' abd pain,- went to ER- U/S, bld work, urine test done-dx miscarriage. 4/18-4/20-pain in hip/waist, little nausea, today blding stopped, still a little nausea/ little pain in hip. EOC was approx 12/09/2021, ct has hx cervical medical issues this past year.


VAERS ID: 1259439 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Missouri  
Vaccinated:2021-04-16
Onset:2021-04-17
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-04-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP7534 / 2 RA / IM

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

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

Write-up: Gravida 2 Para 1 Estimated due date 11/1/2021 Received Pfizer dose # 1 on 3/26/2021 . Relates she started spotting 4/14/21. Was seen by OB 4/15/21 and no heartbeat detected. Patient relates OB advised her to complete covid vaccination as scheduled Pfizer dose # 2 was given 4/16/21 Relates she miscarried on 4/17/21 and was seen in ER.


VAERS ID: 1272570 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-04-02
Onset:2021-04-17
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-04-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / 1 LA / SYR

Administered by: School       Purchased by: ?
Symptoms: Caesarean section, Emergency care, Exposure during pregnancy, Premature delivery
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (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, 7 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: Ceclor, sulpha antibiotics
Diagnostic Lab Data: Countless, can provide if requested.
CDC Split Type:

Write-up: Event: REFRACTORY Pre-Eclampsia (Refractory Hellp Syndrome) Pregnancy History: Second pregnancy, first was a very early miscarriage on 9/11/2020 Due Date: 6/18/2021 Delivery Date: 4/22/2021 (emergency c section) Birth Weight: 3 lb 3.5 ounces


VAERS ID: 1373093 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2021-02-12
Onset:2021-04-17
   Days after vaccination:64
Submitted: 0000-00-00
Entered: 2021-06-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012M20A / 2 LA / IM

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

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: estrogen aspirin
Current Illness: none
Preexisting Conditions: asthma
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: miscarriage 4/18/2021 - 10 weeks pregnant started bleeding on 4/17/2021


VAERS ID: 1381776 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Arkansas  
Vaccinated:2021-04-15
Onset:2021-04-17
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-06-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 044A21A / 2 LA / SYR

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

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: primatial vitamin
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Ultrasound, miscarriage, lab work for hormones, and kept monitoring the bad
CDC Split Type: vsafe

Write-up: Participant was 5 weeks pregnant when she got the shot due date would have been December 9, 2021. April 17th around five o clock started to experience strange feeling so she just continued to rest, said she was spotting heavy and participant got an ultrasound 2 days later and later on during the day said she heavy bleeding still. On April the 22nd the doctor told her she had a miscarriage.


VAERS ID: 1694270 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-03-11
Onset:2021-04-17
   Days after vaccination:37
Submitted: 0000-00-00
Entered: 2021-09-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1805029 / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Bed rest, Blood test, Eosinophil count increased, Foetal death, Foetal heart rate abnormal, Haemorrhage, In vitro fertilisation, Muscle spasms, Pain, Twin pregnancy, Ultrasound foetal abnormal
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Dystonia (broad), Eosinophilic pneumonia (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), Fertility disorders (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? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamin DHA vitamin D estradiol patches 0.1 ml applying them every 3 days for IVF estradiol tablets 2 mg 3x day for IVF
Current Illness: I had a migraine from the estradiol
Preexisting Conditions: diverticulosis
Allergies: no
Diagnostic Lab Data: ultrasound-showed one baby did not have a heartbeat blood work- Eosinophil was high
CDC Split Type: vsafe

Write-up: 03/11/2021 - I was not pregnant at the time of the vaccination. I started taking progesterone injection 2ml a day on 03/20/2021. I did an embryo transfer on 03/25/2021. On 04/17/2021 in the evening, I suddenly stated cramping, I was bent over, it was hurting really bad and shortly after that I started bleeding. I went to the Emergency Room. I''m RH negative blood type, to get a Rhogam shot. I had an ultrasound and I was told I was carrying twins. They also did blood work and my Eosinophil count was high. They both (babies) had heart beats, but one was lower than the other. I was put on bedrest. I saw my fertility doctor on 04/20/2021, the one (baby) where the bleed was coming from no longer had a heartbeat. The other one (baby) did have a good heartbeat. I was put back on bed rest, On the 04/27/2021, I returned to the fertility doctor, and neither one (baby) had a heartbeat anymore.


VAERS ID: 1318393 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-17
Onset:2021-04-17
   Days after vaccination:90
Submitted: 0000-00-00
Entered: 2021-05-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EE8493 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed, Mood altered, SARS-CoV-2 test, Ultrasound uterus
SMQs:, Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Depression (excl suicide and self injury) (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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Lactation decreased; Miscarriage (one previous miscarriage 2020); Miscarriage; Pregnancy
Allergies:
Diagnostic Lab Data: Test Date: 20210420; Test Name: COVID-19 virus test; Test Result: Negative ; Test Name: Ultrasound; Result Unstructured Data: Test Result:Ultrasound confirmed healthy pregnancy; Comments: at 6 weeks then had a further ultrasound bloods and surgery
CDC Split Type: GBPFIZER INC2021480082

Write-up: Mood change; missed miscarriage; This is a spontaneous report from a contactable consumer received. The regulatory authority report number is GB-MHRA-WEBCOVID-202104281636569950-ZM40F. Safety Report Unique Identifier GB-MHRA-ADR 25213374. A 29-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 17Jan2021 (Lot Number: EE8493) as 1ST DOSE, SINGLE for COVID-19 immunisation. Medical history included pregnancy, one previous miscarriage 2020, Lactation decreased, miscarriage. Patient no longer pregnant at the time of reporting. Concomitant medication included folic acid taken for vitamin supplementation. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. The patient experienced mood change on an unspecified date. The patient had vaccine in Jan2021 fell pregnant then at 11.5 weeks. She missed miscarriage at 11.5 weeks pregnant. Ultrasound confirmed healthy pregnancy at 6 weeks then had a further ultrasound bloods and surgery. She had a miscarriage on 17Apr2021 which resulted in surgery to remove it. Patient was exposed to the medicine before pregnancy. The patient underwent lab tests included Negative COVID-19 test on 20Apr2021. The outcome of event missed miscarriage was recovered and another event was unknown. The events were reported as serious, hospitalization, medically significant. The patient received second dose of BNT162B2 on 28Apr2021 (Lot Number: ER9449). No follow up attempts are possible. No further information is expected.


VAERS ID: 1475579 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-23
Onset:2021-04-17
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-07-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW4815 / 1 LA / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Anembryonic gestation, Arthralgia, Maternal exposure during pregnancy, Myalgia
SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ESOMEPRAZOLE
Current Illness: Gastrooesophageal reflux
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: FRPFIZER INC2021796235

Write-up: The pregnancy was discovered between the first and second dose of the vaccine; Anembryonic gestation; spontaneous miscarriage; arthralgia; myalgia; This is a spontaneous report from contactable consumer or other non hcp downloaded from the WEB regulatory authority or other manufacturer number FR-AFSSAPS-CN20212081, Safety Report Unique Identifier FR-AFSSAPS-2021081606. A 28-years-old female patient received bnt162b2 (COMIRNATY), dose 1 intramuscular, administered in Arm Left on 23Mar2021 (Batch/Lot Number: EW4815) as DOSE 1, SINGLE, dose 2 intramuscular, administered in Arm Left on 17Apr2021 (Batch/Lot Number: ER9470) as DOSE 2, SINGLE for covid-19 immunisation. Concomitant drug esomeprazole (ESOMEPRAZOLE), oral from 18Mar2021 (Batch/Lot Number: Unknown) to 18Mar2021, at unspecified dose for an unspecified indication. Medical history included ongoing gastrooesophageal reflux disease. Last menstrual period date 04Mar2021 (the estimated pregnancy date: 18Mar2021). The pregnancy was discovered between the first and second dose of the vaccine. Arrested pregnancy (clear egg), discovered on 28Apr2021 with confirmation on 03May2021, with treatment taken to evacuate. The female patient did not present with adverse reactions during the first injection; arthralgia and myalgia during the 24 hours following the second dose. The patient experienced anembryonic gestation (anembryonic gestation) (medically significant) on 28Apr2021 with outcome of recovered , spontaneous miscarriage (abortion spontaneous) (medically significant) on 28Apr2021 with outcome of recovered , arthralgia (non-serious) on 17Apr2021 with outcome of unknown , myalgia (non-serious) on 17Apr2021 with outcome of unknown. . No follow-up attempts possible. No further information expected. Lot/Batch number already obtained.


VAERS ID: 1237754 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2021-04-02
Onset:2021-04-18
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-04-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / -
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, 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: none
Preexisting Conditions: none
Allergies: minocycline
Diagnostic Lab Data: blood test April 15th, 2021 blood test April 19th, 2021
CDC Split Type:

Write-up: MISCARRIAGE- Conceived and got pregnant March 28. Received 2nd dose of Pfizer vaccine April 2. Found out I was pregnant April 14th, and confirmed it with blood test taken April 15th. HCG levels at 57, putting me at around 3 weeks pregnant. Started bleeding April 18th and doctor confirmed a miscarriage is taking place.


VAERS ID: 1237194 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Maryland  
Vaccinated:2021-04-13
Onset:2021-04-19
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-04-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 044B21A / UNK - / -

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

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

Write-up: Miscarriage


VAERS ID: 1264894 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Maine  
Vaccinated:2021-04-01
Onset:2021-04-19
   Days after vaccination:18
Submitted: 0000-00-00
Entered: 2021-04-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK - / -

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

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

Write-up: Early Miscarriage after vaccine. About 5 weeks pregnant when miscarriage happened.


VAERS ID: 1334056 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-03-20
Onset:2021-04-19
   Days after vaccination:30
Submitted: 0000-00-00
Entered: 2021-05-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Amniocentesis abnormal, Diarrhoea, Fatigue, Pain, Pyrexia, Ultrasound scan
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (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), Noninfectious diarrhoea (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: None
Current Illness: None
Preexisting Conditions: None
Allergies: Amoxicillin
Diagnostic Lab Data: Ultrasound on 5/11/2021 showed a most likely miscarriage: fetus measuring 6 weeks with no heartbeat detected, sac measuring 9 weeks, and some evidence of debris. Follow up HCG levels taken 3 times that week showed a significant drop, confirming the miscarriage.
CDC Split Type:

Write-up: Received second dose of Pfizer on Saturday 3/20/2021. Conceived sometime either right before or in the week after receiving the shot. Had a strong reaction for 3 days that week most likely from the shot (fever, diarrhea, body aches, fatigue) from Wednesday-Friday. I found out at my 9 week prenatal visit that baby was not viable and appeared to have stopped growing at 6 weeks gestation.


VAERS ID: 1424529 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-30
Onset:2021-04-19
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-06-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210521; Test Name: dating ultrasound; Result Unstructured Data: Test Result:miscarriage
CDC Split Type: FRPFIZER INC2021708761

Write-up: Miscarriage; found out she was 2-3 weeks pregnant on 19Apr2021; This is a spontaneous report from a contactable consumer via medical information team for both mother and fetus. This is a Maternal Exposure During Pregnancy, first trimester report. A 28-years-old female pregnant patient received bnt162b2 (COMIRNATY; Solution for injection, Batch/Lot number was not reported),via an unspecified route of administration on 30Mar2021 (at the age of 28-years-old) as Dose 1 ,Single for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. On 19Apr2021, the reporter stated that the patient called in order to know the maximum delay for the second dose. Patient received her 1st dose on 30Mar2021 and should have received the second dose on 20Apr2021. But patient found out she was 2-3 weeks pregnant on 19Apr2021 and the vaccination was postponed. On 21May 2021, during the dating ultrasound, the gynecologist informed her of the miscarriage. The pregnancy resulted in spontaneous abortion. The event miscarriage as serious (medically significant). The patient underwent lab tests and procedures which included ultrasound uterus: miscarriage on 21May2021. The outcome of the events was unknown.


VAERS ID: 1241670 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-03-16
Onset:2021-04-20
   Days after vaccination:35
Submitted: 0000-00-00
Entered: 2021-04-22
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? 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: 4/20/21
CDC Split Type:

Write-up: Miscarriage


VAERS ID: 1309565 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Nebraska  
Vaccinated:2021-04-08
Onset:2021-04-20
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-05-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8729 / 2 LA / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: SERTRALINE; VITAMIN D3; PRENATAL [FOLIC ACID;IRON]
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210423; Test Name: Covid test; Test Result: Negative ; Comments: Nasal Swab
CDC Split Type: USPFIZER INC2021470679

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer (patient). A 30-year-old female patient received BNT162B2 (Pfizer-BioNTech COVID-19 vaccine), the second dose on 08Apr2021 at 07:30 (Lot Number: ER8729) and the first dose on 16Mar2021 at 07:30 (Lot Number: EN6207), both via an unspecified route of administration, administered in the left arm, as a single dose for COVID-19 immunisation. The patient''s medical history was not reported. Concomitant medications included sertraline (manufacturer unknown); vitamin d3 (manufacturer unknown) and folic acid, iron (PRENATAL) all taken for an unspecified indication, start and stop date were not reported. The patient had a miscarriage on 20Apr2021 at 04:30. The patient did not receive any treatment for the event. The event resulted in a visit to the doctor or health care professional office/clinic visit and hospitalization on an unspecified date. The outcome of the event was recovering. The patient had a nasal swab Covid test on 23Apr2021 with a result of negative. No follow-up attempts are needed. No further information is expected.


VAERS ID: 1314678 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Florida  
Vaccinated:2021-03-21
Onset:2021-04-20
   Days after vaccination:30
Submitted: 0000-00-00
Entered: 2021-05-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK LA / SYR

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

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

Write-up: On 04/20/2021 I had a miscarriage I was 6 weeks pregnant. My due date was around Christmas.


VAERS ID: 1330002 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2021-04-03
Onset:2021-04-20
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 043A21A / N/A LA / SYR

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

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

Write-up: estimated to be due December 7, 2021. I didn''t have any symptoms, I didn''t feel like I lost the pregnancy, until we had ultrasound on May 14, 2021


VAERS ID: 1358417 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-02-03
Onset:2021-04-20
   Days after vaccination:76
Submitted: 0000-00-00
Entered: 2021-05-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Fatigue, Pain in extremity, Prenatal screening test, Pyrexia, Stillbirth
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? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
   Extended hospital stay? No
Previous Vaccinations: I had a fever from the seasonal flu shot in the past.
Other Medications: I was taking prenatal vitamins .
Current Illness: None.
Preexisting Conditions: I have fibroids.
Allergies: I am allergiec sulfa drugs
Diagnostic Lab Data: I had my placenta checked and genital checked.
CDC Split Type: vsafe

Write-up: After having a fever of a 101 and I was extreme fatigue, and I also did have soreness in my arm I did have a steel birth on April 28, 2021, autopsy report is still pending.


VAERS ID: 1457638 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-26
Onset:2021-04-20
   Days after vaccination:84
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9262 / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Ectopic pregnancy, Fallopian tube operation, Laboratory test, Malaise, Pain, Thrombosis, Ultrasound scan, Ultrasound scan vagina, Uterine dilation and curettage, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Thrombophlebitis (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Allergy medication Zyrtec
Current Illness:
Preexisting Conditions: Chronic migraines
Allergies: Sulfa Avocado
Diagnostic Lab Data: Transvaginal ultrasound Ultrasound Lab/blood work
CDC Split Type: vsafe

Write-up: On April 12th, I took a pregnancy test and it was positive. I started feeling sick and feeling pain on April 26th. I started bleeding and had blood clots, which continued to April 28th. I went to the ER. I took an ultrasound and took lab work every 3 days. I was told that I may have been having a miscarriage or an ectopic pregnancy. On April 30th, I did lab work. On May 4th, I took a transvaginal and a regular ultrasound. On May 5th, the doctor believed I was having a ectopic pregnancy. On May 6th, I went in for surgery and they had to remove my left fallopian tube. I also had a D&C. I suffered a miscarriage.


VAERS ID: 1711513 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: Nevada  
Vaccinated:2021-03-27
Onset:2021-04-20
   Days after vaccination:24
Submitted: 0000-00-00
Entered: 2021-09-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8733 / 1 RA / -

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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101136390

Write-up: miscarriage; This is a spontaneous report from a contactable consumer (patient). A 42-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8733), via an unspecified route of administration, administered in right arm on 27Mar2021 at 15:00 (at the age of 42-years-old) as dose 1, single for COVID-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient''s medical history and concomitant medications were not reported. The patient had a missed miscarriage on 20Apr2021 at 14:00. The mother reported she became pregnant while taking bnt162b2. The mother was 10 weeks pregnant at the onset of the event. The mother was due to deliver on 10Nov2021. The pregnancy resulted in spontaneous abortion. The event resulted in Emergency room/department or urgent care and was treated with pain medication. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, she has not been tested for COVID-19. The event was resolved.


VAERS ID: 1356652 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-06
Onset:2021-04-20
   Days after vaccination:73
Submitted: 0000-00-00
Entered: 2021-05-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0725-55-102 / 2 RA / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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 INC2021566195

Write-up: I got pregnant after getting the vaccine everything was fine until the pregnancy stopped leading to a complete abortion of the embryo; This is a spontaneous report from a contactable other hcp downloaded from the Regulatory Authority, regulatory authority number IT-MINISAL02-729501. This other hcp reported information for both mother and fetus/baby. This is a maternal report. A 38-years-old female patient received second dose of bnt162b2 (COMIRNATY, PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EL0725-55-102; Expiration Date: 31Mar2021), via an intramuscular route of administration, on Arm Right, on 06Feb2021 09:00, as single dose for COVID-19 immunisation. The patient previously received the first dose of Comirnaty. The patient medical history and concomitant medications were not reported. It was reported that the patient got pregnant after getting the vaccine, everything was fine until the pregnancy stopped leading to a complete abortion of the embryo on 20Apr2021. The pregnancy resulted in spontaneous abortion. The fetal outcome is intrauterine death. Verbatim of Case narrative including clinical course, therapeutic measures, outcome and additional relevant information: Description: 14May2021: with regard to the outcome, it should be noted that it is a miscarriage and not a death of the vaccine recipient as the outcome of the pregnancy is not considered fatal. The first dose was administered on 17Jan2021, lot EL_1484, expiration date 30Apr2021. - Pregnancy (yes) - COVID 19 COMIRNATY (PFIZER) VACCINE: Area of administration (right shoulder) Booster dose number (2) Time of administration (09:00) Lot expiration (31Mar2021) Comment: good morning, after getting the vaccine I got pregnant and lost the baby in my first pregnancy. No follow-up attempts possible. No further information expected.


VAERS ID: 1266336 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-04-21
Onset:2021-04-21
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0162 / 2 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion, Back pain, Exposure during pregnancy, Haemorrhage, Headache, Multigravida, Pregnancy, Pubic pain, Pyrexia, Ultrasound scan, Uterine dilation and curettage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), 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), 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: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Sonogram
CDC Split Type:

Write-up: Pt. started having fever that evening, headache, and lower back pain (significant). Yesterday drove to ER due to continued severe lower back pain and pubic pain. On the way to the ER, she started bleeding a lot. At the hospital, she had a sono and was told she had an abortion. They performed a D&C. She was 10wks. This is 2nd pregnancy, which was uncomplicated pregnancy.


VAERS ID: 1267543 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-04-16
Onset:2021-04-21
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-04-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / IM

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

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

Write-up: Pregnant at the time of vaccination. Miscarriage did occur.


VAERS ID: 1299121 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Florida  
Vaccinated:0000-00-00
Onset:2021-04-21
Submitted: 0000-00-00
Entered: 2021-05-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Off label use
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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021449208

Write-up: The patient was pregnant at the time of vaccination; The patient was pregnant at the time of vaccination; Miscarriage; This is a spontaneous report from a contactable consumer (patient, self-reported). The patient reported information for both herself and fetus/baby. This is a maternal report. A 30-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, on an unknown date, as a single dose for COVID-19 immunization. The patient''s medical history and concomitant medications were not provided. The patient did not receive any other vaccine in four weeks. The patient was not diagnosed with COVID, prior vaccination. The patient was not tested for COVID post vaccination. The patient was pregnant at the time of vaccination. The Patient''s last menstrual date was 09Jan2021 and delivery date was 16Oct2021. The mother reported she became pregnant while taking BNT162B2. The mother was 14 weeks pregnant at the onset of the event. It was reported that on 21Apr2021, the pregnancy resulted in spontaneous abortion- miscarriage and resulted in emergency room and physician visit. Outcome of the event miscarriage was reported as not recovered and for all other events, it was unknown. Information on the lot/batch number has been requested.


VAERS ID: 1336048 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-03-31
Onset:2021-04-21
   Days after vaccination:21
Submitted: 0000-00-00
Entered: 2021-05-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8732 / 1 RA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0172 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Injection site erythema, Injection site induration, Injection site nodule
SMQs:, 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)

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: Levothyroxine; Prenatal vitamins; Vitamin D; Iron supplements.
Current Illness: None
Preexisting Conditions: Hypothyroidism
Allergies: None
Diagnostic Lab Data: Genetic testing on fetus 04/22/2021, results normal fetus with no abnormalities
CDC Split Type:

Write-up: Miscarriage, injection site reaction, 6mm x 8mm hard red knot


VAERS ID: 1410357 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-02-27
Onset:2021-04-21
   Days after vaccination:53
Submitted: 0000-00-00
Entered: 2021-06-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6200 / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Laboratory test, Labour induction, Low birth weight baby, Premature baby, Premature delivery, Premature rupture of membranes
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Neonatal disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 5 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal Vitamins
Current Illness: no
Preexisting Conditions: no
Allergies: no
Diagnostic Lab Data: Hospital - lots of tests April 25th
CDC Split Type: vsafe

Write-up: Premature rupture of membranes prompting admission to hospital - needs steriods for lung maturation for baby - water brook early; pre-term delivery via induction. Yes - first preg.; May 28th - due date - late April was the date of delivery and 4lb. and 5 oz for birth weight - baby was there for 4 weeks. feeding/growing low birth weight; prematurity - was cause of the four weeks.


VAERS ID: 1655725 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Indiana  
Vaccinated:2021-04-09
Onset:2021-04-21
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-08-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 017B21A / 1 RA / SYR
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 040B21A / 2 RA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Dysmenorrhoea, Heavy menstrual bleeding, Loss of personal independence in daily activities, Pregnancy test negative
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Dementia (broad), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Hives from penicillin when I was a very small child, 1980s
Other Medications:
Current Illness: None
Preexisting Conditions: None
Allergies: Penicillin, shellfish
Diagnostic Lab Data:
CDC Split Type:

Write-up: Menstrual cycle completely changed. First cycle after shot in April there were intense cramping, like early contraction type of pains. The volume and length of my cycle was incredibly higher and longer than normal. It was life altering to the point I could not leave the house because I was bleeding so much and had to be close to a bathroom. This continued in May. The cramps were not as bad as April but the volume and length was still unusual. May?s cycle was like my heaviest day for 6 straight days. In June I miscarried at about 6 weeks. July?s cycle seemed closer to normal and now in August I have not gotten a period at all and have tested negative for pregnancy. This shot has most definitely changed my menstrual cycle. For the last 20+ years I am very regular and my cycle typically follows a pattern but since the shot, everything?s changed. I feel this is common enough of a problem it should be looked into more. As a woman, it sure doesn?t feel like any one cares about this aspect of the shot. As a mother of young girls, I want peace of mind when they are eligible for the shot I am not somehow screwing up their little systems long term.


VAERS ID: 1422884 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-21
Onset:2021-04-21
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3001442 / 2 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Headache, Injection site inflammation, Malaise, Myalgia, Pruritus
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Extravasation events (injections, infusions and implants) (broad), Eosinophilic pneumonia (broad), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (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? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: LEVOTHYROXINE
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Disease risk factor
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLMODERNATX, INC.MOD20211

Write-up: Miscarriage; Localized pruritus; Malaise; Myalgia; Headache; This regulatory authority case was reported by a physician and describes the occurrence of ABORTION SPONTANEOUS (Miscarriage) in a 33-year-old female patient who received mRNA-1273 (COVID 19 Vaccine Moderna) (batch nos. 3001442 and 3001941) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included Disease risk factor. Concomitant products included LEVOTHYROXINE from 01-Jan-2001 to an unknown date for an unknown indication. On 21-Apr-2021, the patient received first dose of mRNA-1273 (COVID 19 Vaccine Moderna) (Intramuscular) .5 milliliter. On 19-May-2021, received second dose of mRNA-1273 (COVID 19 Vaccine Moderna) (Intramuscular) dosage was changed to .5 milliliter. On 21-Apr-2021, the patient experienced the first episode of MALAISE (Malaise), the first episode of MYALGIA (Myalgia) and HEADACHE (Headache). On 28-Apr-2021, the patient experienced INJECTION SITE INFLAMMATION. On 29-Apr-2021, the patient experienced the second episode of MALAISE (Malaise). On 19-May-2021, the patient experienced PRURITUS (Localized pruritus) and the second episode of MYALGIA (Myalgia). On 22-May-2021, the patient experienced ABORTION SPONTANEOUS (Miscarriage) (seriousness criterion medically significant). On 21-Apr-2021, HEADACHE (Headache) had resolved. On 29-Apr-2021, last episode of MALAISE (Malaise) had resolved. On 01-May-2021, INJECTION SITE INFLAMMATION had resolved. At the time of the report, ABORTION SPONTANEOUS (Miscarriage), PRURITUS (Localized pruritus) and the last episode of MYALGIA (Myalgia) had resolved. For mRNA-1273 (COVID 19 Vaccine Moderna) (Intramuscular), the reporter did not provide any causality assessments. No treatment information was provided. Very limited information regarding these events have been provided at this time. No further information is expected. Most recent FOLLOW-UP information incorporated above includes: On 19-May-2021: Significant information received. Additional event of ''Malaise'' was added. Case updated accordingly. On 14-Jun-2021: Follow up received. Additional events added, NS to Serious upgrade; Sender''s Comments: Very limited information regarding these events have been provided at this time. No further information is expected.


VAERS ID: 1283215 (history)  
Form: Version 2.0  
Age: 24.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-05
Onset:2021-04-22
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-05-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK LA / SYR

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

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

Write-up: I (unknowingly at the time) was pregnant at the time of my vaccine administration. I didn?t find out until a week or 2 later. My estimate due date was 12/26/2021. I did end up miscarrying this pregnancy on 4/22/2021.


VAERS ID: 1310194 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-04-12
Onset:2021-04-22
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-05-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 037A21B / 1 - / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood creatine, Blood glucose, Blood urea, Exposure during pregnancy, Foetal death, Full blood count, Metabolic function test, Muscle spasms, Rhesus antigen positive, SARS-CoV-2 test, Second trimester pregnancy, Ultrasound antenatal screen abnormal, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Dystonia (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), Normal pregnancy conditions and outcomes (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown but hx shows: Prenatal vitamins, Calcium, Vitamin D, Vitamin B12/B6 levothyroxine, Zantac, Zoloft, Viread, buspirone?
Current Illness: Seizure disorder, depression, hypothyroid, Chronic Hep B, pregnancy
Preexisting Conditions: Seizure disorder, depression, hypothyroid, Chronic Hep B, pregnancy
Allergies: NKA
Diagnostic Lab Data: US 4/22/21 and ER, 4/22/21 CBC, BMP, BUN, Creatinine, Glucose, COVID test
CDC Split Type:

Write-up: Patient had miscarriage after 1st dose of COVID vaccine. Vaginal bleeding and cramping started after routine check at her OB clinic 4/22 showed fetal demise , Miscarriage complete 4/22/21. Seen by provider for pregnancy care per patient. Was around 16 weeks at time of 1st moderna vaccine- G4P1031. ER visit 4/22 reports she was supposed to be 17 weeks on that date but US confirmed fetal demise at 12w6 days. RH positive


VAERS ID: 1317507 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Maryland  
Vaccinated:2021-04-07
Onset:2021-04-22
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-05-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 042A21A / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Foetal death, Intermenstrual bleeding, Nausea, Pyrexia, Ultrasound scan, Vomiting
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), 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), 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? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: codeine
Diagnostic Lab Data: 4.15.21 - ultrasound (baby measuring 8 weeks, 4 day; HR -176 5.11.21 - Ultrasound discovering missed miscarriage at 9 weeks 4 days
CDC Split Type:

Write-up: On 05.11.2021 I went in for an ultrasound due to spotting. I should have been 13 weeks pregnant. The fetus was measuring 9 weeks 4 days which means the fetus died on 4.22.2021. 4.7.21 - received vaccine shot 4.8.21-4.9.21 - fever (used tylonel), nausea, vomiting I had significant nausea and vomiting the week of 4.11.21 - particularly the end of the week. 4.15.21 - ultrasound (baby measuring 8 weeks, 4 day; HR -176) I continued to vomit, though I was able to hold more food down. 4.22.21 the fetus would have been 9.4 days which is when the fetus stopped developing 5.11.21 - Ultrasound discovering missed miscarriage Doctor recommended reporting due to the timing with the vaccine.


VAERS ID: 1371478 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Alabama  
Vaccinated:2021-04-15
Onset:2021-04-22
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-06-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EP6955 / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, 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: Prenatal, Iron supplements, potassium, magnesium, metoprolol, omeprazole, escitalopram
Current Illness:
Preexisting Conditions: Blood Pressure, tachycardia, verge of anemia
Allergies: pineapple, kiwi, steroids'' given via a shot
Diagnostic Lab Data: Blood work, ultrasound
CDC Split Type: vsafe

Write-up: I lost my pregnancy in the early stages at 5 weeks.


VAERS ID: 1578342 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-04-01
Onset:2021-04-22
   Days after vaccination:21
Submitted: 0000-00-00
Entered: 2021-08-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0150 / 1 AR / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0161 / 2 AR / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Pre-natal vitamins
Current Illness:
Preexisting Conditions:
Allergies: Keflex
Diagnostic Lab Data: HCG test for both; miscarriage confirmed with HCG and ultrasound for the second pregnancy
CDC Split Type:

Write-up: Miscarriage 5 days following first dose; conceived again later that month and miscarried ~6 weeks following second dose; ectopic pregnancy 2.5 months after second dose


VAERS ID: 1646985 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Louisiana  
Vaccinated:2021-03-30
Onset:2021-04-22
   Days after vaccination:23
Submitted: 0000-00-00
Entered: 2021-08-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6205 / 2 RA / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Menstruation delayed, Menstruation irregular, Oligomenorrhoea
SMQs:, Termination of pregnancy and risk of abortion (narrow), Fertility 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: MULTIVITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;FOLIC ACID;NICOTINAMIDE;PANTHENOL;RETINOL;RIBOFLAVIN;THI; ARMOUR THYROID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Allergy; Allergy to insect sting; Hashimoto''s disease; Hypothyroidism
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101034010

Write-up: My menstrual cycle came late in April (5weeks); My menstrual cycle came late in April (5weeks) and then I had another cycle 2 weeks later and it lasted 13 days; My cycles have been very irregular since; I became pregnant in June and miscarried; This is a spontaneous report from a contactable consumer (patient). A 38 years old female patient received the second dose of BNT162B2 (Batch/lot number: EN6205) at right arm for COVID-19 immunisation on 30Mar2021 at 15:30 (38 years old at the time of vaccination). The patient was not pregnant at time of vaccination. Relevant history included Hashimitos, hypothyroidism, and allergies: Bactrim, adhesive, wasps. Relevant concomitant drug included Armour Thyroid, multi-vitamin. The patient previously received the first dose of BNT162B2 (Batch/lot number: EN6202) at right arm for COVID-19 immunisation on 09Mar2021 at 15:30. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient''s menstrual cycle came late in April (5weeks) and then she had another cycle 2 weeks later and it lasted 13 days. Her cycles had been very irregular since 22Apr2021. The patient became pregnant in June and miscarried. The outcome of events was unknown. The patient had visited the doctor or other healthcare professional office/clinic visit. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Follow-up attempts are completed. No further information is expected.


VAERS ID: 1311932 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-14
Onset:2021-04-22
   Days after vaccination:39
Submitted: 0000-00-00
Entered: 2021-05-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER1741 / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID; PARACETAMOL
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Delivery; Miscarriage; Pregnancy (uncomplicated); Comments: I am otherwise well with no other medical conditions and not taking regular medications Patient has not had symptoms associated with COVID-19 Not had a COVID-19 test Patient is not enrolled in clinical trial Patient is not currently breastfeeding
Allergies:
Diagnostic Lab Data: Test Date: 20210422; Test Name: scan; Result Unstructured Data: Test Result:unable to confirm viability
CDC Split Type: GBPFIZER INC2021474796

Write-up: miscarriage/ Early miscarriage; This is a spontaneous report from a contactable consumer (patient). This is a report received from the Regulatory Agency. Regulatory authority report number GB-MHRA-WEBCOVID-202104271409519250-UJWAK, Safety Report Unique Identifier GB-MHRA-ADR 25204677. A 33-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 14Mar2021 (Lot Number: ER1741) as 2ND DOSE, SINGLE for COVID-19 immunization. Medical history included miscarriage, previous pregnancy uncomplicated, and delivery in Jan2019. The patient was otherwise well with no other medical conditions and not taking regular medications (as reported). Patient has not had symptoms associated with COVID-19, not had a COVID-19 test, was not enrolled in clinical trial, and not currently breastfeeding. Concomitant medications included folic acid taken for folic acid supplementation on unspecified dates and paracetamol taken for an unspecified indication from 14Mar2021 to 14Mar2021. The patient experienced miscarriage/ early miscarriage on 22Apr2021. Maternal exposure during pregnancy was reported. Patient no longer pregnant at the time of reporting. The clinical course was also reported as follows: The patient had COVID vaccine on 14Mar2021 which was around the time she conceived baby. She was unaware of the pregnancy at the time she had the vaccine and she was not planning a pregnancy either. Had a miscarriage 5-6 weeks following the vaccine. 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). The patient underwent lab tests and diagnostic procedures which included scans on 22Apr2021: unable to confirm viability. Patient has not tested positive for COVID-19 since having the vaccine. The outcome of the event miscarriage/ early miscarriage was recovering. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1363338 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-16
Onset:2021-04-22
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-06-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW9127 / 1 LA / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: URSOFALK
Current Illness: Cholestasis of pregnancy
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: HUPFIZER INC2021599148

Write-up: birth of a dead foetus; This is a spontaneous report received from a contactable physician downloaded from the Regulatory Authority-WEB. The regulatory authority report number is HU-OGYI-334521. A 33-year-old female patient in her 35th week of gravidity received bnt162b2 (COMIRNATY), dose 1 intramuscular, administered in arm left on 16Apr2021 (Batch/Lot Number: EW9127) as 0.3 ml single at the age of 33-year-old for COVID-19 immunisation. Medical history included ongoing cholestasis of pregnancy. Concomitant medication(s) included ursodeoxycholic acid (URSOFALK) taken for cholestasis of pregnancy, start and stop date were not reported. With therapy, her liver enzyme values were satisfactory, serum bilirubin was normal. The patient experienced birth of a dead foetus on 22Apr2021. The mother reported she became pregnant while taking bnt162b2. The mother was 35 weeks pregnant at the onset of the event. The foetus died on an unspecified date. It was not reported if an autopsy was performed. The course of events was as follows: On 20Apr2021 in the evening, the patient started to have abdominal pain, which was similar to menstrual cramps. She was not bleeding, seepage of amniotic fluid was not detected. On 21Apr2021, she has felt foetal movements. On 22Apr2021, she went to the delivery room because of irregular labour-pains, where intrauterine death was verified. Based on the opinion of the patient''s hepatologist, the cholestasis was mild, and URSOFALK was not likely to have contributed to the event. He assumed relationship between the vaccination and foetal death. #Further information is expected. Sender Comment: Foetal death occurred in a female patient vaccinated in the 35th week of her gravidity with the first dose of COMIRNATY. To take out (medicines given to patient on discharge from hospital stay) was 4 days for the beginning of symptoms, and 6 days for foetal death. The patient had cholestasis of pregnancy, and had to take URSOFALK, which might have been also harmful for the foetus. Based on the above, causality between foetal death and COMIRNATY is possible. The case is serious because the foetus died. Further information is expected. No follow-up attempts possible. No further information expected.; Reported Cause(s) of Death: foetal death


VAERS ID: 1472554 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-18
Onset:2021-04-22
   Days after vaccination:35
Submitted: 0000-00-00
Entered: 2021-07-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage; Pregnancy (Patient no longer pregnant at the time of reporting.); Pregnancy
Allergies:
Diagnostic Lab Data: Test Name: Blood test; Result Unstructured Data: Test Result:Unknown results; Test Name: ultrasounds; Result Unstructured Data: Test Result:Unknown results
CDC Split Type: GBPFIZER INC2021776316

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202106240734181040-N2CCC, Safety Report Unique Identifier GB-MHRA-ADR 25532054. A 30-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on 18Mar2021 at dose 2, single for COVID-19 immunisation. Medical history included abortion spontaneous, pregnancy, pregnancy not ongoing (Patient no longer pregnant at the time of reporting). Patient has not had symptoms associated with COVID-19. Not had a COVID-19 test. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Concomitant medication included folic acid taken for vitamin supplementation. The patient previously took folic acid almus for Folic acid supplementation. The patient experienced miscarriage on 22Apr2021. Seriousness criteria reported as other medically important condition. Previously had one miscarriage but was able to see foetus, stopped growing at 7 or 8 weeks. This time nothing to be seen at all. Patient was exposed to the medicine before pregnancy. Pregnancy of unknown location - miscarried naturally blood tests and ultrasounds. Had Pfizer 2-3 weeks before. Patient has not tested positive for COVID-19 since having the vaccine. The patient underwent lab tests and procedures which included blood test and ultrasounds: unknown results on an unspecified date. The outcome of the event was recovered on 01May2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1783541 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-15
Onset:2021-04-22
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-10-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3001653 / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Autopsy, Foetal death, Foetal growth restriction, Foetal hypokinesia, Microbiology test, Placental infarction, Ultrasound Doppler, Ultrasound scan
SMQs:, Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (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? 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: Drug hypersensitivity
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210505; Test Name: Fetal study; Test Result: Positive ; Result Unstructured Data: Macroscopic data: female fetus. Signs of recent retention Intrauterine growth delay without externally or internally visualized malformation. Major placental hypotrophy (less than 8.5 weeks since LMP ) with vascular changes. Samples taken for bacteriological and frozen sample studies. Histological data : ongoing. comment: subject to the state of the fetus. Pregnancy reported at 26.5 since LMP. Biometric characteristics usually consistent with 25th week post-amnenorrhea development; Test Date: 20210505; Test Name: Microbiological lung examination; Test Result: Negative ; Result Unstructured Data: No flora, aerobic bacteria study negative at 5 days. Anaerobic bacteria study negative at 5 days.; Test Date: 20210505; Test Name: Microbiology placenta/cord/membrane examination; Test Result: Positive ; Result Unstructured Data: Some gram-positive bacilli. Aerobic bacteria study: Positive Isolation of Enterococcus faecalis (fair number of colonies) and Proteus mirabilis (fewcolonies).; Test Date: 20210423; Test Name: doppler scan; Result Unstructured Data: Regular fetal heartbeat at 150bpm; Test Date: 20210331; Test Name: Ecography; Test Result: Negative ; Result Unstructured Data: ultrasound of the fetus and its organs that did not reveal any abnormalities. Fetal size consistent with term. Monitoring of morphology and maturation was planned between 26 and 28 weeks since LMP.; Test Date: 20210430; Test Name: Ecography; Test Result: Positive ; Result Unstructured Data: Recent fetal death a few days ago. Multiple placental infarction
CDC Split Type: FRMODERNATX, INC.MOD20213

Write-up: Intrauterine growth retardation; Death intrauterine; Placental infarction; Foetal movements decreased; This case was initially received (Reference number: FR-AFSSAPS-NY20210941) on 04-Oct-2021. The most recent information was received on 04-Oct-2021 and was forwarded to Moderna on 06-Oct-2021. This regulatory authority prospective pregnancy case was reported by a physician and describes the occurrence of FOETAL GROWTH RESTRICTION (Intrauterine growth retardation), FOETAL DEATH (Death intrauterine), PLACENTAL INFARCTION (Placental infarction) and FOETAL HYPOKINESIA (Foetal movements decreased) in a 28-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 3001653) for COVID-19 vaccination. Concurrent medical conditions included Drug hypersensitivity. On 15-Apr-2021, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. The patient''s last menstrual period was on 15-Oct-2020 and the estimated date of delivery was 22-Jul-2021. On 22-Apr-2021, after starting mRNA-1273 (Spikevax), the patient experienced FOETAL HYPOKINESIA (Foetal movements decreased) (seriousness criteria hospitalization and medically significant). On 30-Apr-2021, the patient experienced FOETAL GROWTH RESTRICTION (Intrauterine growth retardation) (seriousness criteria hospitalization and medically significant), FOETAL DEATH (Death intrauterine) (seriousness criteria death, hospitalization and medically significant) and PLACENTAL INFARCTION (Placental infarction) (seriousness criterion hospitalization). The patient received mRNA-1273 (Spikevax) beginning around the twenty-sixth week of the pregnancy. The delivery occurred on an unknown date, which was reported as Intrauterine death. For foetus 1, The outcome was reported as Stillbirth NOS. On 02-May-2021, FOETAL GROWTH RESTRICTION (Intrauterine growth retardation) had not resolved. The patient died on an unknown date. It is unknown if an autopsy was performed. At the time of death, PLACENTAL INFARCTION (Placental infarction) and FOETAL HYPOKINESIA (Foetal movements decreased) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 31-Mar-2021, Ultrasound scan: negative (Negative) ultrasound of the fetus and its organs that did not reveal any abnormalities. Fetal size consistent with term. Monitoring of morphology and maturation was planned between 26 and 28 weeks since LMP.. On 23-Apr-2021, Ultrasound Doppler: normal (normal) Regular fetal heartbeat at 150bpm. On 30-Apr-2021, Ultrasound scan: positive (Positive) Recent fetal death a few days ago. Multiple placental infarction. On 05-May-2021, Autopsy: positive (Positive) Macroscopic data: female fetus. Signs of recent retention Intrauterine growth delay without externally or internally visualized malformation. Major placental hypotrophy (less than 8.5 weeks since LMP ) with vascular changes. Samples taken for bacteriological and frozen sample studies. Histological data : ongoing. comment: subject to the state of the fetus. Pregnancy reported at 26.5 since LMP. Biometric characteristics usually consistent with 25th week post-amnenorrhea development. On 05-May-2021, Microbiology test: negative (Negative) No flora, aerobic bacteria study negative at 5 days. Anaerobic bacteria study negative at 5 days. and positive (Positive) Some gram-positive bacilli. Aerobic bacteria study: Positive Isolation of Enterococcus faecalis (fair number of colonies) and Proteus mirabilis (fewcolonies).. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications listed. No treatment information provided. Company Comment: This case of fetal death/maternal exposure during pregnancy, concerns a 28-year-old female patient (gestational age at the time of exposure to vaccine was 24-26 based on LMP) with no relevant medical history, who experienced the unexpected serious events of placental infarction, fetal hypokinesia, intrauterine growth restriction and fetal death. The events occurred 2 weeks after receiving the Moderna mRNA-1273 vaccine (Spikevax). The rechallenge is not applicable. The benefit-risk relationship of mRNA vaccine is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 04-Oct-2021: Translation received 06-Oct-21: Updated all lab data.; Sender''s Comments: This case of fetal death/maternal exposure during pregnancy, concerns a 28-year-old female patient (gestational age at the time of exposure to vaccine was 24-26 based on LMP) with no relevant medical history, who experienced the unexpected serious events of placental infarction, fetal hypokinesia, intrauterine growth restriction and fetal death. The events occurred 2 weeks after receiving the Moderna mRNA-1273 vaccine (Spikevax). The rechallenge is not applicable. The benefit-risk relationship of mRNA vaccine is not affected by this report.


VAERS ID: 1285423 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Indiana  
Vaccinated:2021-04-22
Onset:2021-04-23
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-05-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 014M20A / 2 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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: Patient developed spotting within 3-4 hours of vaccine administration, and miscarried approximately 24 hours later. Patient was about 7 weeks pregnant at the time of vaccination.


VAERS ID: 1312194 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-04-21
Onset:2021-04-23
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-05-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Dyspnoea, Exposure during pregnancy, Pain, Palpitations, Sleep disorder, Urine analysis, Vaginal haemorrhage
SMQs:, Anaphylactic reaction (broad), Haemorrhage terms (excl laboratory terms) (narrow), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Gummy vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: 4/19/21, 4/20/21, and 4/21/21 hcg urine tests, and 4/30/21 and 5/3/21 blood tests to confirm miscarriage.
CDC Split Type:

Write-up: Miscarriage occurred within 2 days of the vaccine. I have carried 2 out of 3 children to over 8 months, the first a live birth (greater than 7 lb) and the second ended in stillbirth (also greater than 7 lb). I have no history of miscarriage. This was my third pregnancy. I became pregnant in March with positive tests on 4/19, 4/20, and 4/21. I had the Covid vaccine 4/21 and by 4/23 was suddenly in pain and bleeding, which continued for six days, after which my body began to recover. Additionally, I began to suffer breathing trouble, waking in the night, heart pounding (no nightmares or fears) and gasping. Was prescribed two inhalers to recover.


VAERS ID: 1340332 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-04-18
Onset:2021-04-23
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-05-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0164 / 2 LA / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ESTRACE; PROGESTERONE
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210426; Test Name: Ultrasound; Result Unstructured Data: Test Result:Baby stopped growing; Comments: baby stopped growing 5 days after shot,; Test Date: 20210506; Test Name: Ultrasound; Result Unstructured Data: Test Result:Baby stopped growing; Comments: baby stopped growing 5 days after shot,
CDC Split Type: USPFIZER INC2021509131

Write-up: Miscarriage - baby stopped growing 5 days after shot, confirmed with ultrasounds on 4/26 and 5/6; This is a spontaneous report from a contactable consumer (patient). This consumer reported information for both mother and fetus. This is the mother report. A 35-year-old female patient (pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration at the age of 35-year-old administered in arm left on 18Apr2021 09:15 (Lot Number: EW0164) at singe dose, dose 1 via an unspecified route of administration at the age of 35-year-old administered in arm left on 28Mar2021 15:00 (Lot Number: Er8732) at single dose for covid-19 immunisation. The patient medical history was not reported. There was no Covid prior vaccination. Concomitant medications included estradiol (ESTRACE), progesterone. There was no other vaccine in four weeks. On 23Apr2021, 14:00, the patient experienced miscarriage - baby stopped growing 5 days after shot, confirmed with ultrasounds on 26Apr2021 and 06May2021. The event resulted in doctor or other healthcare professional office/clinic visit. Last menstrual date was 10Mar2021. There was no Covid test post vaccination. There was no treatment for event. The outcome of event was recovering.; Sender''s Comments: Linked Report(s) : PFIZER INC-2021512724 baby case


VAERS ID: 1368713 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2021-04-22
Onset:2021-04-23
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-06-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 048B21A / 2 LA / SYR

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Exposure during pregnancy, Fatigue, Intermenstrual bleeding, Pyrexia, Uterine contractions during pregnancy
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), 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), Normal pregnancy conditions and outcomes (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: High blood pressure medication (Nisedipine er30mg tablets and Ladetalol hcl 300mg prenatal vitamin
Current Illness: none
Preexisting Conditions: High blood pressure
Allergies: penicillin
Diagnostic Lab Data: Took blood to get blood type.
CDC Split Type: vsafe

Write-up: Fever took Tylenol Very tired Starting spotting lightly was 10 weeks pregnant The spotting became like a period Labor contractions Miscarried at 12 weeks


VAERS ID: 1398763 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-03-19
Onset:2021-04-23
   Days after vaccination:35
Submitted: 0000-00-00
Entered: 2021-06-15
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: Amniorrhoea, Blood test normal, Exposure during pregnancy, Gynaecological examination normal, Pathology test, Premature baby, Premature delivery, Secretion discharge, 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), Foetal disorders (narrow), Neonatal disorders (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? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Zoloft 100mg Prenatal vitamin Fish oil
Current Illness: None
Preexisting Conditions: Depression
Allergies: Sulfa
Diagnostic Lab Data:
CDC Split Type:

Write-up: Prior to the vaccination I had a normal pregnancy. This was my first pregnancy. . No issues with me or fetus. I did receive the flu vaccine in the fall of 2020 but no other vaccines or medications than those previously reported. On 4/23/2021 I began experiencing a small amount of bloody discharge which continued for 10 days. I was evaluated in OB triage on 5/5 by exam, blood work and ultrasound. All tests came back normal and the pathology from discharge was blood and mucus. The discharge continued until 2 weeks later on 5/19 when it became brighter red. I was evaluated by OB triage again by exam and blood work with normal results. Cervix showed no signs of labor and I was not dilated. On 5/20 I began leaking amniotic fluid and my water broke. My son was born at 30 weeks and 3 days (due date 7/26/2021). He is in NICU as of this report but doing as well as could be expected.


VAERS ID: 1379609 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-05
Onset:2021-04-23
   Days after vaccination:77
Submitted: 0000-00-00
Entered: 2021-06-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK4244 / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021584448

Write-up: Maternal exposure during pregnancy; Miscarriage; First dose on 05Feb2021, second dose on 23Apr2021; First dose on 05Feb2021, second dose on 23Apr2021; This is a spontaneous report from a contactable consumer. This is a report received from a regulatory authority (RA). Regulatory authority report number: GB-MHRA-WEBCOVID-202105221119451640-ANKK6, Safety Report Unique Identifier: GB-MHRA-ADR 25343276. A 22-year-old female patient received the BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration first dose (Lot number Ek4244) on 05Feb2021 and second dose (Lot number ER1749) on 23Apr2021; both given at single dose for COVID-19 immunization. Medical history was not reported. Patient has not had symptoms associated with COVID-19 and has not had a COVID-19 test. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Concomitant medication included folic acid taken for folic supplementation. Patient was exposed to the medicine before pregnancy. The patient experienced maternal exposure during pregnancy on an unspecified date and miscarriage on 14May2021. The events were assessed as serious by reporter: congenital anomaly and medically significant. Patient was no longer pregnant at the time of reporting. Patient has not tested positive for COVID-19 since having the vaccine. The outcome of events was unknown. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1401416 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-23
Onset:2021-04-23
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3001941 / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Injection site pain, Maternal exposure during pregnancy
SMQs:, 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)

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: Maternal vaccine exposure (COVID-19 vaccine exposure during pregnancy week: 3)
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLMODERNATX, INC.MOD20212

Write-up: This regulatory authority retrospective pregnancy case was reported by a consumer and describes the occurrence of ABORTION SPONTANEOUS in a 35-year-old female patient who received mRNA-1273 (COVID 19 Vaccine Moderna) (batch no. 3001941) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included Maternal vaccine exposure (COVID-19 vaccine exposure during pregnancy week: 3). On 23-Apr-2021, the patient received first dose of mRNA-1273 (COVID 19 Vaccine Moderna) (Intramuscular) 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 23-Apr-2021, the patient experienced INJECTION SITE PAIN. On 18-May-2021, the patient experienced ABORTION SPONTANEOUS (seriousness criterion medically significant). On an unknown date, the patient experienced MATERNAL EXPOSURE DURING PREGNANCY. The delivery occurred on an unknown date, which was reported as Spontaneous Abortion. The outcome was reported as Spontaneous Abortion NOS. On 27-Apr-2021, INJECTION SITE PAIN had resolved. At the time of the report, ABORTION SPONTANEOUS and MATERNAL EXPOSURE DURING PREGNANCY outcome was unknown. The action taken with mRNA-1273 (COVID 19 Vaccine Moderna) (Intramuscular) was unknown. Concomitant product was not provided by the reporter. Treatment information was not provided. Company Comment: Causality for event Maternal exposure during pregnancy is not applicable. Based on the current available information and temporal association between the use of the product and the start date of the events Abortion spontaneous and Injection site pain, a causal relationship cannot be excluded.; Sender''s Comments: Causality for event Maternal exposure during pregnancy is not applicable. Based on the current available information and temporal association between the use of the product and the start date of the events Abortion spontaneous and Injection site pain, a causal relationship cannot be excluded.


VAERS ID: 1323598 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-04-23
Onset:2021-04-24
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-05-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0170 / 2 LA / IM

Administered by: Military       Purchased by: ?
Symptoms: Abortion spontaneous, Asthenia, Blood test, Dizziness, Exposure during pregnancy, Fatigue, Full blood count, Muscle spasms, Nausea, Pyrexia, Ultrasound abdomen, Vaginal haemorrhage, Vomiting
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dystonia (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (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), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: OTC prenatal vitamin, calcium supplement, and probiotic
Current Illness: None
Preexisting Conditions: None
Allergies: Sulfa drug allergy, nickel metal allergy
Diagnostic Lab Data: ER visit Abdominal ultrasound HCG quant lab CBC w diff labs
CDC Split Type:

Write-up: The day following my vaccination (4/24/21) I awoke feeling completely nauseous and dizzy. Upon getting out of bed I immediately sat on the floor due to the extreme dizziness and fear of passing out I felt. After a few minutes in this state I vomited. I had a fever which I managed with Tylenol. I felt fatigued and weak the entire day. I ran a fever the entire day, again managing it with Tylenol. The following day (4/25/2021) my fever was gone and I felt better, however about midday I began experiencing cramps and vaginal bleeding. I was 5.5weeks pregnant with an estimated due date of 12/24/2021. I went to the ER with concerns of a miscarriage. Based on abdominal ultrasound and subsequent HCGquant testing over the next week it was determined I had encountered a miscarriage and lost the baby.


VAERS ID: 1367797 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-04-22
Onset:2021-04-24
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-06-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ERH735 / 2 RA / SYR

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

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

Write-up: Two days following the vaccine, I had a miscarriage . I was 8 weeks pregnant.


VAERS ID: 1413092 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: California  
Vaccinated:2021-03-08
Onset:2021-04-24
   Days after vaccination:47
Submitted: 0000-00-00
Entered: 2021-06-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6206 / 1 LA / IM
IPV: POLIO VIRUS, INACT. (IPOL) / SANOFI PASTEUR EP6955 / 2 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Ultrasound scan abnormal, Uterine dilation and curettage, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Malignancy related therapeutic and diagnostic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal Vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: Amoxicillin
Diagnostic Lab Data: Ultrasound confirming pregnancy loss- May 4th, 2021 Pathology Reports from D&C- May 11th, 2021
CDC Split Type:

Write-up: I found out I was pregnant on March 3rd, 2021 from an at-home pregnancy test. The pregnancy was confirmed with blood work on March 6th, 2021. I received my first dose of the covid vaccine on March 8th, 2021. I noticed some light spotting afterwards. The heartbeat was confirmed on March 22nd and I was told I was six weeks along. I received my second dose on March 29th. The heartbeat was confirmed again during another ultrasound on April 20th, 2021. During an ultrasound on May 4th, 2021 I was told that there was no longer a heartbeat and the baby had stopped developing a week prior. This missed miscarriage resulted in an D&C on May 11th, 2021.


VAERS ID: 1511599 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-04-24
Onset:2021-04-24
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 037A21B / 2 LA / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Fatigue, Gait disturbance, Maternal exposure during pregnancy, Myalgia, Pregnancy test, Vertigo
SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Vestibular disorders (narrow), 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), Hypoglycaemia (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 [FOLIC ACID;IRON]; CITRANATAL ASSURE
Current Illness:
Preexisting Conditions: Comments: No medical history was provided by the reporter.
Allergies:
Diagnostic Lab Data: Test Date: 20210513; Test Name: pregnancy test; Test Result: Positive ; Result Unstructured Data: positive
CDC Split Type: USMODERNATX, INC.MOD20211

Write-up: Sore arm after vaccination; tiredness; Today she woke up and felt she wasn''t going to be able to walk with her normal balance, she felt she had to grab on to something.; vertigo; Seven weeks pregnant and had Moderna vaccine administered; This spontaneous prospective pregnancy case was reported by a consumer and describes the occurrence of ABORTION SPONTANEOUS in a 38-year-old female patient (gravida 3) who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 037A21B and 02021A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was provided by the reporter. Concomitant products included FOLIC ACID, IRON (PRENATAL [FOLIC ACID;IRON]) and CITRANATAL ASSURE for an unknown indication. On 24-Apr-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-May-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 24-Apr-2021, the patient experienced MATERNAL EXPOSURE DURING PREGNANCY (Seven weeks pregnant and had Moderna vaccine administered). On 13-May-2021, the patient experienced VERTIGO (vertigo). On 01-Jun-2021, the patient experienced GAIT DISTURBANCE (Today she woke up and felt she wasn''t going to be able to walk with her normal balance, she felt she had to grab on to something.). On 06-Jul-2021 at 4:00 AM, the patient experienced ABORTION SPONTANEOUS (seriousness criterion medically significant). On an unknown date, the patient experienced ABDOMINAL PAIN, MYALGIA (Sore arm after vaccination) and FATIGUE (tiredness). On 24-Apr-2021, MATERNAL EXPOSURE DURING PREGNANCY (Seven weeks pregnant and had Moderna vaccine administered) had resolved. At the time of the report, ABORTION SPONTANEOUS, VERTIGO (vertigo), GAIT DISTURBANCE (Today she woke up and felt she wasn''t going to be able to walk with her normal balance, she felt she had to grab on to something.), ABDOMINAL PAIN, MYALGIA (Sore arm after vaccination) and FATIGUE (tiredness) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 13-May-2021, Pregnancy test: positive (Positive) positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No treatment medications were reported. concomitant products included vitapol ultra. Company Comment: This case concerns a 38-year-old female patient who received mRNA-1273 while 7 weeks pregnant. Obstetric and gynecological history was not provided. Maternal exposure during pregnancy is assessed as not applicable. The other events show temporal association between the use of mRNA-1273 and the onset. Hence causal relationship cannot be excluded. Fatigue and myalgia are consistent with product known safety profile. This case was linked to MOD-2021-193546 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 21-Jul-2021: Follow up information was received 21 Jul 2021 wherein ADR form received. Patient demographics updated, concomitant medications, vaccination details, new events added. HCP contact details provided, updated pregnancy information :Birth type and fetal out come and gestation period details.; Sender''s Comments: This case concerns a 38-year-old female patient who received mRNA-1273 while 7 weeks pregnant. Obstetric and gynecological history was not provided. Maternal exposure during pregnancy is assessed as not applicable. The other events show temporal association between the use of mRNA-1273 and the onset. Hence causal relationship cannot be excluded. Fatigue and myalgia are consistent with product known safety profile


VAERS ID: 1552827 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Alabama  
Vaccinated:2021-03-01
Onset:2021-04-24
   Days after vaccination:54
Submitted: 0000-00-00
Entered: 2021-08-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 1 AR / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 2 AR / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Caesarean section, Exposure during pregnancy, Haemorrhage, Internal haemorrhage, Muscle spasms, Pain, Panic attack, Premature delivery, Premature separation of placenta, Tremor
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Hypoglycaemia (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 10 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamins, Tylenol
Current Illness: Pregnancy, sciatica
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: 4/24/21 they found the concealed abruption during c section. Baby had to go to icu for 10 days. I was treated intravenously with antibiotics and lots of fluid due to my blood loss.
CDC Split Type:

Write-up: On the night of the 23rd, I was having severe cramping that I assumed was Braxton Hicks contractions. I called early morning on the 24th. I was instructed to go in to labor and delivery immediately. I had a scheduled c section on 5-5-21. So we were only 37 weeks. I had uncontrollable shaking which my doctor thought was due to a panic attack because I have past anxiety and depression. They tried to check my cervix and my back was uncontrollably straightening out and I had no control over my body. My doctor was about to send me home but decided it would be best to do a c section. They waited until another c section was finished. I had no bleeding, I was just in pain. When they did the c section, the found that I had a concealed abruption and was internally bleeding. I lost a lot of blood. My doctor told me this is rare and normally happens with drug addicts, not healthy women in pregnancy. My baby almost died. She had to be resuscitated because all the blood that was in her lungs due to my placenta tear from the uterine wall. This is my third baby and I?ve never had any issues or health problems while pregnant. I did not have gestational diabetes. Even at birthweight at 37 weeks premature, she was born at 8 pounds 4 ounces. No one knows what happened.


VAERS ID: 1662690 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2021-02-24
Onset:2021-04-24
   Days after vaccination:59
Submitted: 0000-00-00
Entered: 2021-09-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 016M20A / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test abnormal, Oral pruritus, Pregnancy test positive, Pruritus, Throat irritation, Tongue pruritus
SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (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? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Modern Vaccine both doses - Itchy face, mouth, tongue, and throat.
Other Medications: None
Current Illness: None
Preexisting Conditions: None aware
Allergies: Bananas, Polymyxin B-Trimethorim, COVID Vaccine
Diagnostic Lab Data: Blood work confirmed pregnancy and loss of pregnancy. There is on going testing to determine if there are any other causes for the losses.
CDC Split Type:

Write-up: I had 2 miscarriages between 5-7wks gestation. 4/24/21 and 7/7/21


VAERS ID: 1742392 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Guam  
Vaccinated:2020-12-21
Onset:2021-04-24
   Days after vaccination:124
Submitted: 0000-00-00
Entered: 2021-09-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EH9899 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0140 / 2 LA / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Human chorionic gonadotropin abnormal, Ultrasound foetal abnormal
SMQs:, Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lisinopril, Carvedilol
Current Illness:
Preexisting Conditions: Hypertension
Allergies: None
Diagnostic Lab Data: FIRST TRIMESTER MISCARRIAGE CONFIRMED POST VACCINE BY ULTRASOUND AND BETA HCG, 4/27/21, 5/13/21, 5/19/21 Patient is recovering from physical and emotional trauma. Will continue to follow.
CDC Split Type:

Write-up: FIRST TRIMESTER MISCARRIAGE


VAERS ID: 1286536 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-02-03
Onset:2021-04-25
   Days after vaccination:81
Submitted: 0000-00-00
Entered: 2021-05-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025J20-2A / 2 - / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test normal, Exposure during pregnancy, Full blood count, Induced labour, Premature rupture of membranes
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? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A - Hx of autoimmune (leaky gut) digestive functioning issues that were treated and improved with specific diet.
Allergies: N/A
Diagnostic Lab Data: No signs of infection from CBC panel of blood cells. Initial placenta pathology found trace staph (not bad one) outside the placenta. No infection or abnormalities of the placenta aside from acute abruption as noted above. Bloodwork from 10 weeks, 11 weeks, 15 weeks, and 17 weeks was all normal. Additional rule out bloodwork outstanding per patients request.
CDC Split Type:

Write-up: 2nd Trimester Miscarriage of Healthy Baby 2nd pregnancy, no hx of miscarriage prior, full term pregnancy with first. All genetic testing on mom and additional health screens of baby were normal. On 4/25/21, lost mucus plug in the AM at 17 weeks pregnant with no other issues, concerns, abnormalities, etc. At 3:50AM on 4/27/21, ruptured membrane/water broke. Hospital testing confirmed 100% break of amniotic fluid with nothing left to sustain baby who had normal heartbeat and was still alive - measuring on target. Induced at 11:20pm on the 27th and delivered at 5:30am on 4/28/21 at 17 weeks and 3 days a baby boy measuring 8.25 inches and 5.6 ounces. No placental infection or abnormalities. Pathology noted an abruption hematoma that could have resulted from induced labor. No trauma, blood work, or other explanations for early rupture of what was a perfectly healthy and growing baby.


VAERS ID: 1323420 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-04-22
Onset:2021-04-25
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-05-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN EW0171 / 1 LA / IM

Administered by: Pharmacy       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:
Current Illness:
Preexisting Conditions: Asthma
Allergies:
Diagnostic Lab Data:
CDC Split Type: vsafe

Write-up: At the time of the J&J vaccine I was 6 weeks pregnant. 3 days after my J&J vaccine, I suffered a miscarriage.


VAERS ID: 1334132 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Florida  
Vaccinated:2021-04-10
Onset:2021-04-25
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-05-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 8729 / 1 LA / SYR

Administered by: Other       Purchased by: ?
Symptoms: Abortion induced, Chills, Exposure during pregnancy, Flushing, Human chorionic gonadotropin abnormal, Hypertension, Infection, Pharyngitis streptococcal, Pyrexia, Vaginal haemorrhage
SMQs:, Anaphylactic reaction (broad), Agranulocytosis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal infections (narrow), Hypertension (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), 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: N/a
Current Illness: N/a
Preexisting Conditions: N/a
Allergies: N/a
Diagnostic Lab Data:
CDC Split Type:

Write-up: Found out I was pregnant day after shot week later I was bleeding for 3 days kind of like a period then it stopped on the 25 I started having high fevers chills facial flushing went to walk in clinic on 27 said I have strep throat took antibiotics 5 days in still having fever chills flushing went to primary dr did blood work showed I had infection blood pressure started becoming high went to obgyn pregnancy hormone low was told not a good pregnancy on 5/14 went to have pregnancy terminated blood pressure very high on 5/17 back at primary dr with high fever chills facial flushing again blood pressure still high put on a water pill to control blood pressure went back to obgyn everything good from procedure hormone levels almost back to zero


VAERS ID: 1307381 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-03-06
Onset:2021-04-26
   Days after vaccination:51
Submitted: 0000-00-00
Entered: 2021-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1802070 / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound scan vagina
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
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data: vaginal ultrasound 4/26/2021 and 5/10/2021
CDC Split Type:

Write-up: conceived 10- 12 days after vaccine shot administered and ultimately had a miscarriage in first trimester


VAERS ID: 1310166 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-01
Onset:2021-04-26
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-05-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / 1 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal
Current Illness: None
Preexisting Conditions: None
Allergies: Penicillin, doxycycline, flexiril
Diagnostic Lab Data: 4/26 had ultrasound which showed the baby stopped growing and was only measuring around a little more than 6 weeks when the gestational sac was measuring a little more than 9 weeks. Also the baby had no heart beat. Based off my last period should have been around 10 weeks pregnant. 4/26 repeat hcg was performed and was I believe 8 or 10K. First one done on 3/10 was around 21K. Another hcg was performed on 4/28 which showed a lower hcg I believe 7K. Unable to check exact labs right now due to entire system being down.
CDC Split Type:

Write-up: Adverse event miscarriage. First pregnancy. Estimated due date middle of November. Received vaccine approximately around 7 weeks of pregnancy. Post vaccination had chills and fatigue starting 12 hours after vaccine lasting about 48 hours.


VAERS ID: 1314848 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-01
Onset:2021-04-26
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-05-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8730 / 1 RA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal
Current Illness: n/a
Preexisting Conditions: gestational diabetes in previous pregnancies; 2
Allergies: sulfa, hayfever
Diagnostic Lab Data: ultra sound
CDC Split Type: vsafe

Write-up: 4/1/2021 vaccination 4/26/2021 MISCARRIAGE *Fetus died 2 days after the vaccine; 4/3/2021; per medical staff (ultra sound). Went to midwife then OB. Dr. did 2nd scan to verify the first scan. Pregnancy HX; 3rd pregnancy, 10/8/2021; 16.5 weeks pregnant at time of miscarriage


VAERS ID: 1329479 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-09
Onset:2021-04-26
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 1 LA / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021498747

Write-up: Early pregnancy miscarriage; 2 lumps near neck; This is a spontaneous report from a contactable consumer (patient). A 31-years-old pregnant female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration, administered in Arm Left on 09Apr2021 at 16:00 (Batch/Lot Number: Unknown) 1ST DOSE, SINGLE for covid-19 immunization. Facility where the most recent COVID-19 vaccine was administered was a Pharmacy or Drug Store. The patient medical history was not reported. There were no concomitant medications. No other vaccines were given within 4 weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. On 26Apr2021, The patient experienced early pregnancy miscarriage, 2 lumps near neck. The patient reported she became pregnant while taking bnt162b2. The mother was 5 Weeks pregnant at the onset of the event and was due to deliver on 22Dec2021. The adverse events resulted in a Doctor or other healthcare professional office/clinic visit. The clinical outcome of the event was reported as not recovered.; Sender''s Comments: Linked Report(s) : US-PFIZER INC-2021501603 baby case


VAERS ID: 1351372 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Georgia  
Vaccinated:2021-04-10
Onset:2021-04-26
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-05-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK RA / SYR

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

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

Write-up: Was 6 weeks pregnant at time of the shot (4/10); missed miscarriage diagnosed on 5/10. 10 weeks. Embryo had stopped developing. 8 to 8.5 weeks (a few days after the prior ultrasound on 4/23 which still indicated normal development of the pregnancy), ca. two weeks after the vaccine. Not sure if the pregnancy loss is related to the vaccine, but reporting after being advised to do so by a representative of the v-safe program.


VAERS ID: 1357263 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Alabama  
Vaccinated:2021-03-18
Onset:2021-04-26
   Days after vaccination:39
Submitted: 0000-00-00
Entered: 2021-05-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6203 / 2 RA / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? 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: No
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021545831

Write-up: Date of start of drug: 25Jan2021, Dose Number: 1; Date of start of drug: 18Mar2021, Dose Number: 2; Miscarriage; This is a spontaneous report from a contactable consumer (patient) reported herself. A 26-years-old female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Right on 18Mar2021 01:00 PM (Batch/Lot Number: EN6203) as 2ND DOSE, SINGLE for covid-19 immunisation, at the age at vaccination date of 26 years old. Patient was not pregnant. Medical history reported as no. The patient''s concomitant medications were not reported. No other vaccine in four weeks. No other medications in two weeks. No known allergies. Historical vaccine included first dose of BNT162B2 (lot number: En6203) on 25Jan2021 01:00 PM at left arm. The patient experienced miscarriage (medically significant) on 26Apr2021 with outcome of recovered, date of start of drug: 25jan2021, dose number: 1; date of start of drug: 18mar2021, dose number: 2 (non-serious) on an unspecified date with outcome of unknown. The event miscarriage resulted in Doctor or other healthcare professional office/clinic visit. No treatment received. Prior to vaccination, the patient was not diagnosed with COVID-19/ Since the vaccination, the patient has not been tested for COVID-19. Follow-up attempts completed. No further information expected.


VAERS ID: 1361671 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Louisiana  
Vaccinated:2021-03-26
Onset:2021-04-26
   Days after vaccination:31
Submitted: 0000-00-00
Entered: 2021-05-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

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

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamins and Progresterone
Current Illness: Had a miscarriage after 2nd dosage 4/23/2021
Preexisting Conditions: Had a miscarriage after 2nd dosage 4/23/2021
Allergies:
Diagnostic Lab Data: A miscarriage
CDC Split Type:

Write-up: Had my first vaccine dosage on 3/26/2021, second dosage on 4/23/2021. I did last ultrasound on 4/22/201, baby was measuring 8 weeks and 4 days with a heartbeat of 174. The baby stop growing 9 weeks and 1 day on 4/26/2021.


VAERS ID: 1464098 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: D.C.  
Vaccinated:2021-04-08
Onset:2021-04-26
   Days after vaccination:18
Submitted: 0000-00-00
Entered: 2021-07-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 003B21A / 2 AR / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Exposure during pregnancy, Polyhydramnios, Premature delivery, Ultrasound antenatal screen abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 4 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Diagnosed with severe polyhydramnios following ultrasound on May 28, 2021.
CDC Split Type:

Write-up: Developed severe polyhydramnios (excess amniotic fluid) and gave birth prematurely. Son was born at 27 weeks gestation; birth weight 2 pounds, 11 oz.


VAERS ID: 1465138 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2021-02-26
Onset:2021-04-26
   Days after vaccination:59
Submitted: 0000-00-00
Entered: 2021-07-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9264 / 1 RA / -
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6201 / 2 RA / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Cimzia, Propranolol, Hydroxychloroquine, Vitamin B6, Unisom, Tylenol
Current Illness: n/a
Preexisting Conditions: Rheumatoid Arthritis, Migraines
Allergies: Diclofenac
Diagnostic Lab Data: Autopsy completed on 4/30/21
CDC Split Type:

Write-up: Adverse Event: Stillbirth at 36 weeks gestation First pregnancy, normal previously Due date: 5/26/21 Delivery Date: 4/28/21 Fetal Demise determined on 4/26/21 Birth Weight: 6lbs, 2oz


VAERS ID: 1636762 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: New York  
Vaccinated:2021-04-15
Onset:2021-04-26
   Days after vaccination:11
Submitted: 0000-00-00
Entered: 2021-08-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH PFIZERER8731 / 1 LA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH PFIZEREW0182 / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Discharge, Exposure during pregnancy, Fatigue, Foetal growth abnormality, Foetal heart rate abnormal, Immediate post-injection reaction, Pain in extremity, Ultrasound foetal abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad)

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

Write-up: Signs of miscarriage 8 days after the vaccine. Had my first ultrasound on 4/6/2021, heard the heart bit. Based on doctors recommendation scheduled the COVID vaccine. First doze administered was on 4/15/2021, immediate side effects were sore arm and felt tired only that day. On 4/24/2021 started getting unusual discharge, no bleeding but brown color. Saw my doctor on 4/27/2021, ultrasound showed no heartbeat and that the baby stopped growing after the first appointment. There was no development after the 8th week.


VAERS ID: 1415761 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-26
Onset:2021-04-26
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Inappropriate schedule of product administration, Maternal exposure during pregnancy, SARS-CoV-2 test, Ultrasound scan
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Medication errors (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID; PREGNACARE ORIGINAL [ASCORBIC ACID;BETACAROTENE;BIOTIN;CALCIUM PANTOTHENATE;COLECALCIFEROL;COPPER;CY
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid supplementation; Lactation decreased; Miscarriage; Pregnancy
Allergies:
Diagnostic Lab Data: Test Name: Blood test; Result Unstructured Data: Test Result:Early miscarriage at 7 weeks pregnant.; Comments: .; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:Early miscarriage at 7 weeks pregnant.
CDC Split Type: GBPFIZER INC2021657702

Write-up: Miscarriage; Maternal exposure during pregnancy; First dose on 01eb2021, second dose on 26Apr2021; This is a spontaneous report from a contactable consumer (patient) received from a regulatory authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202106041702385750-DT4TR. Safety Report Unique Identifier GB-MHRA-ADR 25422309. A 34-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration at the age of 34-year-old on 26Apr2021 (Lot Number: Not Known) as 2ND DOSE, SINGLE for covid-19 immunisation. Medical history included abortion spontaneous, pregnancy in 2015, lactation decreased, folic acid supplementation. Concomitant medication included folic acid (FOLIC ACID) taken for pregnancy and vitamin supplementation from 01Mar2021 to an unspecified stop date; ascorbic acid, betacarotene, biotin, calcium pantothenate, colecalciferol, copper, cyanocobalamin, folic acid, iodine, iron, magnesium, nicotinamide, phytomenadione, pyridoxine hydrochloride, riboflavin, selenium, thiamine mononitrate, tocopheryl acid succinate, zinc (PREGNACARE ORIGINAL [ASCORBIC ACID;BETACAROTENE;BIOTIN;CALCIUM PANTOTHENATE;COLECALCIFEROL;COPPER;CYANOCOBALAMIN;FOLIC ACID;IODINE;IRON;MAGNESIUM;NICOTINAMIDE;PHYTOMENADIONE;PYRIDOXINE HYDROCHLORIDE;RIBOFLAVIN;SELENIUM;THIAMINE MONONITRATE;TOCOPHERYL) taken for pregnancy from 01Jan2021 to an unspecified stop date. The patient previously took dose 1 of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), on 01Feb2021 for covid-19 immunisation and experienced no adverse event. The patient experienced miscarriage (congenital anomaly) on 14May2021 with outcome of recovered on 21May2021, maternal exposure during pregnancy on 26Apr2021 with outcome of unknown. Event miscarriage was reported as serious with medically significant and congenital anomaly. Event maternal exposure during pregnancy was reported as serious with medically significant. The patient underwent lab tests and procedures which included blood test: early miscarriage at 7 weeks pregnant, COVID-19 virus test: no - negative, ultrasound scan: early miscarriage at 7 weeks pregnant, all on an unknown date. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Patient has not tested positive for COVID-19 since having the vaccine. Clinical course reported as follows: Vaccine received the day before getting a positive pregnancy test. Pregnancy progressing as expecting until week 7 where I started bleeding. Confirmed with hospital that I was miscarrying - side effect from vaccine. Did the medicine have an adverse effect on any aspect of the pregnancy: Unsure. Details of previous pregnancies: Previous healthy pregnancy in 2015.Patient was exposed to the medicine first-trimester (1-12 weeks). Details of scans or investigations: Early miscarriage at 7 weeks pregnant. Had second dose of vaccine the day before finding out I was pregnant on 26Apr2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1454965 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-15
Onset:2021-04-26
   Days after vaccination:70
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL8723 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Pregnancy test, 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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Delivery (have given birth to two healthy children)
Allergies:
Diagnostic Lab Data: Test Date: 20210325; Test Name: Pregnancy test; Test Result: Positive ; Test Date: 20210415; Test Name: Ultrasound; Result Unstructured Data: Test Result:An amniotic sac and the yolk sac were visible; Comments: however, a heartbeat could not yet be detected
CDC Split Type: DEPFIZER INC2021752812

Write-up: Miscarriage in the 9th week of pregnancy (missed abortion); This is a spontaneous report from a non-contactable consumer downloaded from a regulatory authority-WEB. The regulatory authority report number is DE-PEI-CADR2021066808. Additional reference numbers included: DE-CADRPEI-2021066808 and DE-PEI-202100059889. A 33-year-old female patient received bnt162b2 (COMIRNATY; Batch/Lot Number: EL8723), via an unspecified route of administration, on 15Feb2021, as dose 2, single for COVID-19 immunisation. Medical history included a delivery from an unknown date and unknown wherein the patient has given birth to two healthy children. The patient has no known allergies, no risk factors and pre-existing conditions. On 26Apr2021, it was reported that on 15Feb2021, the patient received the second vaccine dose and Early to mid-March the patient was became pregnant. (The first day of her last period was 25Feb2021). The first positive pregnancy test was on 25Mar2021. The patient had her first appointment with the gynaecologist on 15Apr20a21. An amniotic sac and the yolk sac were visible on ultrasound, however, a heartbeat could not yet be detected. At the next follow-up appointment in the 9th week of pregnancy (on 26Apr2021) it was established that the embryo was no longer alive (missed abortion). On 29Apr2021 a womb scrape (curettage) was thereupon carried out in hospital. No explainable causes were found for the miscarriage. The patient was aware that pregnancy terminations often happened during early pregnancy. However, as the patient had not suffered a miscarriage until then and have given birth to two healthy children, the patient reported the incident. Even if the patient did not assume that the incident has anything to do with the vaccination, she still considered it sensible to report such serious events that have taken place within a short time of the vaccination. The outcome of the event was recovered on unspecified date in 2021. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1479511 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-31
Onset:2021-04-26
   Days after vaccination:85
Submitted: 0000-00-00
Entered: 2021-07-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Lactation decreased
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021852456

Write-up: Amenorrhea; miscarriage; This is a spontaneous report from a contactable consumer or other non hcp received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202107031131114520-PLG8K, Safety Report Unique Identifier GB-MHRA-ADR 25590299. A 42-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number was not reported) via an unspecified route of administration on 31Jan2021 (at the age of 42-years-old) as first dose, single for COVID-19 immunization. Medical history included suppressed lactation from an unknown date and unknown if ongoing. Patient had no 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 miscarriage on 26Apr2021 and amenorrhea on 30May2021. Additional information was as follows: Chemical pregnancy/miscarriage 26/4/21. Patient had not tested positive for COVID-19 since having the vaccine. Suspect Reactions. Any relevant investigations or tests conducted was reported as none. The outcome of miscarriage was unknown and amenorrhea was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1837558 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-23
Onset:2021-04-26
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ET3045 / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Myalgia
SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (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? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Pregnancy
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC202101395081

Write-up: Myalgia/muscle pain; Belly ache/abdominal pain; Miscarriage; This is a spontaneous report from a non-contactable consumer downloaded from the Regulatory Agency (RA)-WEB, regulatory authority number DE-PEI-CADR2021065146. A 31-year-old female patient received BNT162B2 (COMIRNATY), via an unspecified route of administration on 23Apr2021 (Lot Number: ET3045) as 0.3ml, single dose for covid-19 immunisation. Medical history included ongoing pregnancy. The patient''s concomitant medications were not reported. On 26Apr2021, the patient experienced myalgia and belly ache. Only muscle pain at first. Suddenly abdominal pain/muscle pain of different tissues persisting to this day. On unspecified date in 2021, the patient experienced miscarriage (medically significant). The mother reported she became pregnant while taking BNT162B2. The mother was 2 months pregnant at the onset of the event. The outcome of the events myalgia and belly ache was recovered on 05May2021, of the event miscarriage was unknown. Sender Comment: Details of risk factors or previous illnesses: None. Only muscle pain at first. Suddenly abdominal pain/muscle pain of different tissues persisting to this day. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1313020 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Illinois  
Vaccinated:2021-04-14
Onset:2021-04-27
   Days after vaccination:13
Submitted: 0000-00-00
Entered: 2021-05-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0162 / UNK RA / -

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? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]
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 INC2021470815

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer (patient herself). A 30-year-old female patient. A 30-year-old pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in right deltoid on 14Apr2021 (Batch/Lot Number: Ew0162) as 2nd dose, single for COVID-19 immunisation. Patient had no relevant medical history. Concomitant medication included minerals nos, vitamins nos (PRENATAL VITAMINS) received within 2 weeks of vaccination. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. She received an unspecified vaccine on 14Apr2021 (same date) in right arm. The patient was not diagnosed with COVID-19 prior to vaccination. The patient experienced miscarriage on 27Apr2021. At 6 weeks there was a heartbeat detected. Patient received her second dose and at 8 weeks there was no heartbeat. Abortion pill was reported as treatment. Event result in Doctor or other healthcare professional office/clinic visit. Patient had not been tested for COVID-19 since the vaccination. Outcome of event was recovering.


VAERS ID: 1323194 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Oklahoma  
Vaccinated:2021-03-18
Onset:2021-04-27
   Days after vaccination:40
Submitted: 0000-00-00
Entered: 2021-05-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 032M20A / 1 LA / SYR
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 031A21A / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Human chorionic gonadotropin positive, Ultrasound scan vagina
SMQs:, Tumour markers (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: Pre-natal vitamins, baby aspirin
Current Illness:
Preexisting Conditions:
Allergies: Avocado
Diagnostic Lab Data: April 27 TVUS measured fetus at 6w1d (behind what was expected given LMP, should have measured 7w2d), embryonic cardiac activity was present, but could not be documented by M-mode April 27 blood draw, HCG levels 28,247H April 29 blood draw, HCG levels 29,925H May 6 TVUS showed no fetal heart tones, and and fetus still measured 6w1d, unchanged from last visit May 13 TVUS showed gestational sac was gone and endometrium was less than 1cm in thickness.
CDC Split Type:

Write-up: Missed miscarriage. LMP March 7, positive pregnancy test on March 31. COVID vaccinations on March 18 and April 22. April 27, first ultrasound measured fetus at 6w1d (behind what was expected given LMP, should have measured 7w2d), embryonic cardiac activity was present, but could not be documented by M-mode. Provider warned 60% chance of abnormal pregnancy. BetaHCG testing results: April 27 was 28,247H; April 29 was 29,925H. A follow-up ultrasound on May 6 showed no fetal heart tones, and and fetus still measured 6w1d, unchanged from last visit. Provider prescribed misoprostol which was taken same day (May 6) to complete the miscarriage. Follow-up ultrasound May 13 showed gestational sac was gone and endometrium was less than 1cm in thickness.


VAERS ID: 1330783 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: New York  
Vaccinated:2021-04-19
Onset:2021-04-27
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0169 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0182 / 2 LA / IM

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

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

Write-up: Patient had an intrauterine fetal demise at 40 5/7 weeks. Most likely unrelated but wanted it reported that she had vaccine during pregnancy.


VAERS ID: 1389288 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-20
Onset:2021-04-27
   Days after vaccination:66
Submitted: 0000-00-00
Entered: 2021-06-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6200 / 2 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN5318 / 1 LA / IM

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

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

Write-up: Fetal demise at 16 weeks


VAERS ID: 1372607 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-27
Onset:2021-04-27
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Inappropriate schedule of product administration, Off label use, SARS-CoV-2 test, Scan
SMQs:, Termination of pregnancy and risk of abortion (narrow), Medication errors (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: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid supplementation; Lactation decreased; Miscarriage; Pregnancy
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test; Test Name: scan; Result Unstructured Data: Test Result:missed miscarriage; Comments: 12 weeks scan detected missed miscarriage; Test Date: 20210430; Test Name: scan; Result Unstructured Data: Test Result:no foetal heart beat; Comments: there was not foetal heart beat at 12 week scan, despite baby growing to that date.; Test Date: 20210514; Test Name: scan; Result Unstructured Data: Test Result:confirmed missed miscarriage; Comments: "Second scan on 14May2021 confirmed missed miscarriage and still no change in passing this"
CDC Split Type: GBPFIZER INC2021575196

Write-up: missed miscarriage; Miscarriage of pregnancy; first dosefirst dose of BNT162B2 on 12Jan2021, received second dose on 27Apr2021; first dosefirst dose of BNT162B2 on 12Jan2021, received second dose on 27Apr2021; This is a spontaneous report from a contactable consumer. This is a report received from the Regulatory authority, report number GB-MHRA-WEBCOVID-202105192122065660-HJBY2, Safety Report Unique Identifier GB-MHRA-ADR 25324665. A 39-year-old female patient (not currently breastfeeding) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot number was not reported), via an unspecified route of administration on 27Apr2021 as second dose, single for COVID-19 immunisation. Medical history included one previous miscarriage, decreased lactation, three successful pregnancies, folic acid supplementation. She had previously given with Flu vaccine (reported as miscarriage about 9 years ago shortly after receiving the flu vaccine). She had her first dose of BNT162B2 on 12Jan2021. Patient has not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. Concomitant medication included folic acid for vitamin supplementation, start and stop date were not reported. It was reported that the patient was exposed to the medicine (vaccine) in her first trimester (1-12 weeks). The patient experienced miscarriage of pregnancy on 30Apr2021. At 12 weeks, scan detected missed miscarriage (unknown date). Three days after vacation (30Apr2021) there was no foetal heart beat at 12 week scan, despite baby growing to that date and miscarriage has not occurred naturally- still awaiting this to happen. The second scan was on 14May2021 and confirmed missed miscarriage and still no change in passing this. The events were reported as serious medically significant. The outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1546252 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-10
Onset:2021-04-27
   Days after vaccination:76
Submitted: 0000-00-00
Entered: 2021-08-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EX0893 / 2 LA / OT
UNK: VACCINE NOT SPECIFIED (NO BRAND NAME) / UNKNOWN MANUFACTURER UNKNOWN / UNK - / 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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Ectopic pregnancy; Factor XI deficiency
Allergies:
Diagnostic Lab Data: Test Date: 20210427; Test Name: kinetics of beta-human chorionic gonadotropin; Result Unstructured Data: Test Result:Miscarriage was confirmed
CDC Split Type: FRPFIZER INC202100966956

Write-up: spontaneous miscarriage; This is a spontaneous report from a contactable consumer downloaded from a regulatory authority-WEB FR-AFSSAPS-PV20212049. A 27-year-old female patient received bnt162b2 (COMIRNATY), dose 2 intramuscular, administered in left arm on 22Apr2021 (Lot Number: EX0893) as 0.3 mL single for COVID-19 immunisation; methotrexate sodium (METHOTREXATE), intracervical on 10Feb2021 (Batch/Lot Number: Unknown), at unspecified dose for ectopic pregnancy. Medical history included ectopic pregnancy from 10Feb2021 to an unknown date (medical termination at 6 weeks with injection of methotrexate (dose and specialty not known) intra-cervical) and factor XI deficiency from an unknown date and unknown if ongoing. The patient''s concomitant medications were not reported. On 19Mar2021, 1st injection of the vaccine bnt162b2 (COMIRNATY) for covid-19 immunisation and also the date of last menstrual period. The mother was due to deliver on 24Dec2021. The patient experienced spontaneous miscarriage on 27Apr2021 (reported as between 5 weeks and 6 weeks) with outcome of recovered. The patient goes to the Emergency Room then returns home. Miscarriage was confirmed on the kinetics of beta-human chorionic gonadotropin (validated by a clinical pathologist). The action taken for methotrexate sodium was unknown. At the time of the declaration on 21Jul2021, patient is again pregnant (currently at 6 weeks); had a 1st ultrasound that did not show any abnormalities. OVERALL, spontaneous miscarriage approximately 2 and a half months after the administration of intra-cervical METHOTREXATE for an ectopic pregnancy, and 6 days after the 2nd injection of the bnt162b2 vaccine against Covid-19 in a 27-year-old patient.


VAERS ID: 1274550 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Maryland  
Vaccinated:2021-04-23
Onset:2021-04-28
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR

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

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

Write-up: Loss of 5 week embryo, which had been PGS-tested without any genetic abnormalities and transferred via IVF on April 14, 2021. Have had one successful pregnancy in past and four other miscarriages, though this is first through IVF with PGS testing.


VAERS ID: 1275897 (history)  
Form: Version 2.0  
Age: 45.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-04-23
Onset:2021-04-28
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-05-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8737 / 1 - / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8736 / 2 - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal death, Motor dysfunction, Ultrasound abdomen
SMQs:, Peripheral neuropathy (broad), Akathisia (broad), Dyskinesia (broad), Dystonia (broad), Parkinson-like events (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)

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:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient was a 45 y/o, G2P0, 39.3 weeks gestation, IVF pregnancy with Gestational Diabetes that was controlled with diet and gestational hypertension. Pt had history of 1 spontaneous abortion. EDD 4/30/21. Pt received her second dose of Pfizer COVID 19 Vaccine on 4/23/21, on that same day she had an ultrasound to check on fetus and fetus received a Biophysical Profile Score of 8/8. On Monday, 4/26/21, pt went to hospital complaining of decreased fetal movement, ultrasound confirmed an intrauterine fetal demise. Pt delivered via C-Section on 4/27/21, birth weight of baby was 8 pounds 12oz.


VAERS ID: 1282583 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: New York  
Vaccinated:2021-04-23
Onset:2021-04-28
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-05-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8735 / 2 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test abnormal, Foetal growth restriction, Ultrasound scan abnormal
SMQs:, Malignancy related therapeutic and diagnostic procedures (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Nature?s Made Pre-Natal Vitamin
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: - 4/22/21: Pregnancy confirmed through blood tests, urine sample, and ultrasound. - 4/28/21: Pregnancy miscarriage confirmed through blood test and ultrasound. - 4/28/21: Dr said the baby stopped growing on either 4/22 or 4/23. 2nd COVID vaccine was administered on 4/23.
CDC Split Type:

Write-up: Miscarriage. I was 5 weeks pregnant at the time of the 2nd Pfizer COVID vaccine on 4/23/21. On 4/22/21, the pregnancy was confirmed by Ob/Gyn through a blood test, urine sample, and ultrasound. I was at the time and am a healthy 30 year old woman without pre-existing medical conditions or any conditions that would put me into a high-risk pregnancy category. The estimated due date was 12/20/21. Received 2nd COVID on 4/23/21. At 3:30pm on 4/28/21, I began miscarrying the pregnancy. On the same day at 4pm, I was at Ob/Gyn and they confirmed that the pregnancy was likely miscarrying through an ultrasound and blood tests. IMPORTANT: On 4/28/21, the pregnancy measured exactly the same in size as it did on 4/22/21. In other words, the pregnancy either STOPPED growing the SAME DAY it was confirmed or the EXTACT NEXT DAY, which was the day I received the 2ND COVID VACCINE. I discussed with my Doctor wither to proceed with the 2nd Covid vaccine and it was suggested that while it hasn?t been tested extensively in pregnancy, it was thought to be safe.


VAERS ID: 1317790 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-20
Onset:2021-04-28
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-05-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 1W0153 / 2 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Haemorrhage, Muscle spasms, Ultrasound scan abnormal
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Malignancy related therapeutic and diagnostic procedures (narrow), Dystonia (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal, synthroid, dexilant
Current Illness: n/a
Preexisting Conditions: Hashimoto, GERD
Allergies: adhesive in bandages
Diagnostic Lab Data: Ultra Sound
CDC Split Type: vsafe

Write-up: 4/20 vaccination 4/28 Started bleeding, cramping 4/29 persistent cramping, bleeding. I went to the ER and had had blood work done the day before positive 4.5 -5 weeks pregnant. *CHEMICAL MISCARRIAGE


VAERS ID: 1329438 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: New York  
Vaccinated:2021-04-23
Onset:2021-04-28
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8735 / 2 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Pregnancy test urine, Ultrasound foetal
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? Yes
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: Test Date: 20210422; Test Name: blood test; Result Unstructured Data: Test Result:Confirmed pregnancy; Test Date: 20210422; Test Name: urine test; Result Unstructured Data: Test Result:Confirmed pregnancy; Test Date: 20210422; Test Name: ultrasound; Result Unstructured Data: Test Result:Confirmed pregnancy
CDC Split Type: USPFIZER INC2021494131

Write-up: Miscarriage / pregnancy loss; This is a spontaneous report from a contactable consumer (patient). This consumer reported information for both mother and fetus. This is the maternal report. A 30-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration (at the age of 30-years-old), administered in Arm Left on 23Apr2021 10:00 (Lot Number: ER8735) as 2nd dose, single for COVID-19 immunization. The patient''s medical history was not reported. Concomitant medication included Nature Made Pre-Natal Vitamin. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Left on 02Apr2021 12:00 (Lot Number: EL9263) as 1st dose, single for COVID-19 immunization. Confirmed pregnancy on 22Apr2021 at OBGYN via blood test, urine test, and ultrasound. Pfizer 2nd dose COVID vaccine administered on 23Apr2021. Began miscarriage on 28Apr2021. On 28Apr2021, OGBYN medical professionals detected NO GROWTH since 22Apr2021 ultrasound. Identical imagining in size. The adverse event resulted in Doctor or other healthcare professional office/clinic visit. The patient experienced miscarriage / pregnancy loss on 28Apr2021 15:30.No treatment received for the event. The mother reported she became pregnant while taking bnt162b2. The mother was 6 Weeks pregnant at the onset of the event. The mother was due to deliver on 20Dec2021. The pregnancy resulted in spontaneous abortion. The outcome of the event was recovering. The event was considered as serious (disability, congenital anomaly). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Information on Lot/Batch number was available. Additional information has been requested.; Sender''s Comments: Linked Report(s) : US-PFIZER INC-2021497434 fetal case


VAERS ID: 1377825 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-04-27
Onset:2021-04-28
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-06-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FW0171 / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Trisomy 22, Ultrasound scan, Ultrasound scan vagina, Uterine dilation and curettage
SMQs:, Congenital, familial and genetic disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins each day, Fluoxitine 30 mg/day
Current Illness: None
Preexisting Conditions: Asthma, depression, anxiety, overweight
Allergies: Sensitivity to Bactrim
Diagnostic Lab Data: Bedside Ultrasound 5/17/2021 - no fetal pole Transvaginal Ultrasound 5/19/2021 - no fetal pole and no growth since appx 5w6d HCG blood test 5/17/2021 - reduced HCG levels
CDC Split Type:

Write-up: Missed miscarriage due to nonmosaic Trisomy 22 (confirmed by genetic testing) on or around 4/28/2021 resulting in D&C procedure on 5/25/2021. I have had one other confirmed miscarriage due to blighted ovum in November 2020, a live birth in December 2018, and a live birth in April 2008.


VAERS ID: 1772215 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Illinois  
Vaccinated:2021-03-31
Onset:2021-04-28
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-10-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 030B21A / 1 LA / SYR
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 002C21A / 2 LA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Menstrual disorder, Menstruation delayed, Pregnancy
SMQs:, Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Fertility disorders (broad)

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

Write-up: I had my last period about 3 days before my second shot. At the time, I was using Nuvaring for birth control, and had just put my Nuvaring in after my period when I got my second vaccine. Thirty days later, when I pulled the ring out to induce my period, I did not get my period. After waiting seven days, I then put my next Nuvaring in. I waited thirty days, and I again pulled the ring out to induce my period. I did not get my period. During my next cycle, I did not put my Nuvaring back in. I became pregnant. I then promptly miscarried. Since then, I have not had a normal cycle.


VAERS ID: 1777968 (history)  
Form: Version 2.0  
Age: 20.0  
Sex: Female  
Location: Guam  
Vaccinated:2021-04-06
Onset:2021-04-28
   Days after vaccination:22
Submitted: 0000-00-00
Entered: 2021-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER87729 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0172 / 2 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, First trimester pregnancy, Foetal heart rate abnormal, Haemorrhage in pregnancy, Human chorionic gonadotropin abnormal, Injury, Maternal exposure before pregnancy, Muscle spasms, Ultrasound foetal abnormal
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Dystonia (broad), Accidents and injuries (narrow), Hostility/aggression (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), Normal pregnancy conditions and outcomes (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: anxiety, depression
Allergies: none
Diagnostic Lab Data: FIRST TRIMESTER MISCARRIAGE CONFIRMED POST VACCINE BY ULTRASOUND AND BETA HCG Patient is recovering from physical and emotional trauma. Will continue to follow.
CDC Split Type:

Write-up: LMP 8/3/2021 patients states bleeding and cramping consistent with miscarriage starting on 10/8/2021 negative fetal heart tone on ultrasound


VAERS ID: 1348389 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-28
Onset:2021-04-28
   Days after vaccination:59
Submitted: 0000-00-00
Entered: 2021-05-25
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: GBPFIZER INC2021522525

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202105091937526420-V6FF9, Safety Report Unique Identifier GB-MHRA-ADR 25268444. A female patient (mother) of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration at 1st dose, single on 28Feb2021 for COVID-19 immunisation. Patient has not had symptoms associated with COVID-19. Not had a COVID-19 test. Patient is not enrolled in clinical trial. The patient medical history and patient''s concomitant medications were not reported. It was reported that the patient had the Pfizer vaccine on the same day, or day before she conceived. She have since miscarried on 28Apr2021. The patient do not necessarily believed that the vaccine caused her miscarriage, but wished to report this in cause there is a correlation between vaccination and miscarriage. The outcome of the event was recovering (as reported). Patient has not tested positive for COVID-19 since having the vaccine. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Sender''s Comments: Since the reporter denies Causality between Vaccination and Miscarriage, the event of Miscarriage is assessed as not related to BNT162B2.


VAERS ID: 1501691 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-28
Onset:2021-04-28
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3001658 / 2 LA / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Human chorionic gonadotropin, Pregnancy test, 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? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]; IRON
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: In vitro fertilization (due to male factor)
Allergies:
Diagnostic Lab Data: Test Date: 202105; Test Name: HCG; Result Unstructured Data: 18 to 21 MAY, HCG Level dropping from 43000 to 39000; Test Date: 20210419; Test Name: Pregnancy test; Test Result: Positive ; Result Unstructured Data: Positive; Test Date: 20210510; Test Name: Ultrasound; Result Unstructured Data: No fetal pole; Test Date: 20210525; Test Name: Ultrasound; Result Unstructured Data: Small fetal pole but no heartbeat
CDC Split Type: CAMODERNATX, INC.MOD20210

Write-up: Miscarriage; Received vaccine while pregnant; Sore at injection site; This spontaneous prospective pregnancy case was reported by a consumer and describes the occurrence of ABORTION SPONTANEOUS (Miscarriage) in a 35-year-old female patient who received mRNA-1273 (Moderna CoviD-19 Vaccine) (batch nos. 3001658 and 3002331) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included In vitro fertilization (due to male factor). Concomitant products included IRON for Iron deficiency, MINERALS NOS, VITAMINS NOS (PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]) for Prenatal care. On 28-Apr-2021 at 11:00 AM, the patient received first dose of mRNA-1273 (Moderna CoviD-19 Vaccine) (Intramuscular) .5 ml. On 27-May-2021 at 11:00 AM, received second dose of mRNA-1273 (Moderna CoviD-19 Vaccine) (unknown route) dosage was changed to .5 ml. The patient''s last menstrual period was on 25-Mar-2021 and the estimated date of delivery was 30-Dec-2021. On 28-Apr-2021, the patient experienced EXPOSURE DURING PREGNANCY (Received vaccine while pregnant) and VACCINATION SITE PAIN (Sore at injection site). On 25-May-2021, the patient experienced ABORTION SPONTANEOUS (Miscarriage) (seriousness criterion medically significant). The patient received mRNA-1273 (Moderna CoviD-19 Vaccine) beginning around the fourth week of the pregnancy. On 28-Apr-2021, EXPOSURE DURING PREGNANCY (Received vaccine while pregnant) had resolved. On 25-May-2021, ABORTION SPONTANEOUS (Miscarriage) had resolved. At the time of the report, VACCINATION SITE PAIN (Sore at injection site) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 19-Apr-2021, Pregnancy test: positive (Positive) Positive. On 10-May-2021, Ultrasound scan: no fetal pole (abnormal) No fetal pole. In May 2021, Human chorionic gonadotropin: decreased (Low) 18 to 21 MAY, HCG Level dropping from 43000 to 39000. On 25-May-2021, Ultrasound scan: small fetal pole but no heartbeat (abnormal) Small fetal pole but no heartbeat. The action taken with mRNA-1273 (Moderna CoviD-19 Vaccine) (Intramuscular) and mRNA-1273 (Moderna CoviD-19 Vaccine) (Unknown Route) was unknown. For mRNA-1273 (Moderna CoviD-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. The patient had no chronic or long-standing health conditions (diabetes, seizure disorder, hypertension, mental health disorders, asthma, etc.). Miscarriage detected at 7 weeks. Confirmed at 9 weeks. Treatment information was not provided. Company Comment This is a case of Maternal exposure during pregnancy with associated AEs (Abortion spontaneous and vaccination site pain) for this 35-year-old female. Further information has been requested. This case was linked to MOD-2021-187441 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 28-May-2021: Internal review on 23-JUL-2021 resulted in update to Pregnancy Information - fetal outcome, gestation period, added event- spontaneous abortion, case upgraded to serious; Sender''s Comments: This is a case of Maternal exposure during pregnancy with associated AEs (Abortion spontaneous and vaccination site pain) for this 35-year-old female. Further information has been requested.


VAERS ID: 1274336 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: New Mexico  
Vaccinated:2021-04-08
Onset:2021-04-29
   Days after vaccination:21
Submitted: 0000-00-00
Entered: 2021-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 AR / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Anembryonic gestation, Exposure during pregnancy, Physical examination, Pregnancy test urine positive, Ultrasound antenatal screen abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
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: None.
Allergies: NKDA
Diagnostic Lab Data: 3/10/21 patient had a routine and normal physical wellness exam. Started on prenatal vitamins at this time. 4/23/21 positive pregnancy test
CDC Split Type:

Write-up: Healthy young women of 25 years of age with spontaneous pregnancy. Regular period prior to becoming pregnant. Patient had miscarriage on 04/29/21 with anembryonic pregnancy. Anembryonic pregnancy confirmed by ultrasound on 4/23/21. Covid vaccine received on 4/8/21. Patient roughly 4 wks pregnancy at time of vaccine dose.


VAERS ID: 1287331 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: California  
Vaccinated:2021-03-26
Onset:2021-04-29
   Days after vaccination:34
Submitted: 0000-00-00
Entered: 2021-05-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK - / -

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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt with miscarriage at approx 7-8 weeks GA after J&J covid vaccine 3/26/21 LMP 2/27/21


VAERS ID: 1301453 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-25
Onset:2021-04-29
   Days after vaccination:63
Submitted: 0000-00-00
Entered: 2021-05-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 042L20A / 1 LA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011A21A / 2 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Multivitamin gummies, vitamin D, Infliximab
Current Illness:
Preexisting Conditions: Ulcerative colitis
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: First day of my last period was Feb 11, 2021. I was pregnant for 11 weeks, and had a miscarriage on April 29, 2021.


VAERS ID: 1306935 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-04-28
Onset:2021-04-29
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Chills, Dizziness, Exposure during pregnancy, Human chorionic gonadotropin, Pyrexia, Ultrasound scan, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Vestibular disorders (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), 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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: HCG, Beta Quant, Serum: 05/03/2021 9 mIU/mL 05/01/2021 20 mIU/mL Ultrasound 5/1/21 Result: No intrauterine pregnancy and no evidence for ectopic pregnancy
CDC Split Type:

Write-up: 5 weeks pregnant, due date December 29, 2021. Next day after the vaccine fever 102.2 for 24 hrs, chills, dizziness, heavy bleeding the day after. Confirmed miscarriage on May 1st.


VAERS ID: 1307914 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: South Dakota  
Vaccinated:2021-04-23
Onset:2021-04-29
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 041B21A / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Dizziness, Haemorrhage, Human chorionic gonadotropin, Muscle spasms
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Anticholinergic syndrome (broad), Dystonia (broad), 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? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data: Blood tests to check Hcg levels among other things in my blood
CDC Split Type:

Write-up: Miscarriage less than a week after the second vaccine with Moderna. Estimated due date 01/07/2022, started with extreme dizziness and ended with Contraction like cramps and bleeding. History of very healthy full term pregnancies.


VAERS ID: 1347279 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-03-18
Onset:2021-04-29
   Days after vaccination:42
Submitted: 0000-00-00
Entered: 2021-05-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 040A21A / 1 LA / SYR
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 016B21A / 2 LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Advair for asthma. Singular for asthma. Prenatal vitamins.
Current Illness: No.
Preexisting Conditions: No.
Allergies: None.
Diagnostic Lab Data: Ultrasound performed on 5/20/21 showing pregnancy loss and embryo dating 6 weeks gestation. Blood tests on 5/21/21 and 5/24/21 showing hCG levels decreasing from 56,000 mIU/mL to 44,000 mIU/mL confirming the miscarriage.
CDC Split Type:

Write-up: Was 0 weeks pregnant at the time of the first shot and 4 weeks pregnant at the time of the second dose of the moderna Covid vaccine. At the 9 week ultrasound I was diagnosed with a missed miscarriage in which the embryo died at 6 weeks gestation. Cause of the miscarriage is own known. Occurred 2 weeks after second covid vaccine dose.


VAERS ID: 1372094 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Florida  
Vaccinated:2021-04-15
Onset:2021-04-29
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-06-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 041B21A / 1 LA / IM

Administered by: Pharmacy       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? 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:
CDC Split Type:

Write-up: Patient was pregnant at time of vaccination (1 week) and proceeded to have a miscarriage 3 weeks following vaccination.


VAERS ID: 1407884 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Florida  
Vaccinated:2021-04-15
Onset:2021-04-29
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-06-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 041B21A / 1 LA / IM

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

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

Write-up: Patient was newly pregnant at time of vaccination. After about 2 weeks of receiving the first Moderna vaccine, patient had a miscarriage. Patient would have been between 4 to 8 weeks pregnant at time of miscarriage.


VAERS ID: 1624186 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: New York  
Vaccinated:2021-04-28
Onset:2021-04-29
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-08-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
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: Light allergy to oyster
Diagnostic Lab Data:
CDC Split Type:

Write-up: I got my second dose on Wednesday Apr 28th. I was a few weeks pregnant (last menstruation 5weeks prior the shot). On Thursday the 29th and Friday the 30th I had cramps. I lost a bit of blood on Saturday May 1rst and a lot of blood (miscarriage) on Sunday May 2nd. I wasn?t pregnant anymore on Monday the 3rd


VAERS ID: 1366616 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-24
Onset:2021-04-29
   Days after vaccination:36
Submitted: 0000-00-00
Entered: 2021-06-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Arthralgia, Body temperature, Chills, Fatigue, Headache, Injection site pain, Injection site pruritus, Maternal exposure during pregnancy, Myalgia, Pyrexia
SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Eosinophilic pneumonia (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Maternal vaccine exposure (COVID-19 vaccine exposure during pregnancy week: 6-7)
Allergies:
Diagnostic Lab Data: Test Date: 20210429; Test Name: Body temperature; Test Result: Inconclusive ; Result Unstructured Data:
CDC Split Type: NLMODERNATX, INC.MOD20211

Write-up: Miscarriage; Maternal exposure during pregnancy; Injection site pruritus; Headache; Fatigue; Chills; Pyrexia; Myalgia; Injection site pain; Generalized joint pain; This regulatory authority case was reported by a consumer and describes the occurrence of ABORTION SPONTANEOUS (Miscarriage) in a 34-year-old female patient who received mRNA-1273 (COVID 19 Vaccine Moderna) (batch no. 3001653) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included Maternal vaccine exposure (COVID-19 vaccine exposure during pregnancy week: 6-7) on 24-Mar-2021. On 24-Mar-2021, the patient received first dose of mRNA-1273 (COVID 19 Vaccine Moderna) (unknown route) .5 milliliter. On 29-Apr-2021, received second dose of mRNA-1273 (COVID 19 Vaccine Moderna) (unknown route) dosage was changed to 1 dosage form. On 29-Apr-2021, the patient experienced MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy), INJECTION SITE PRURITUS (Injection site pruritus), HEADACHE (Headache), FATIGUE (Fatigue), CHILLS (Chills), PYREXIA (Pyrexia), MYALGIA (Myalgia), INJECTION SITE PAIN (Injection site pain) and ARTHRALGIA (Generalized joint pain). On 01-May-2021, the patient experienced ABORTION SPONTANEOUS (Miscarriage) (seriousness criterion medically significant). On 30-Apr-2021, HEADACHE (Headache) had resolved. On 01-May-2021, PYREXIA (Pyrexia), MYALGIA (Myalgia) and ARTHRALGIA (Generalized joint pain) had resolved. On 02-May-2021, INJECTION SITE PRURITUS (Injection site pruritus), FATIGUE (Fatigue) and INJECTION SITE PAIN (Injection site pain) had resolved. On 08-May-2021, ABORTION SPONTANEOUS (Miscarriage) had resolved. At the time of the report, MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy) outcome was unknown and CHILLS (Chills) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 29-Apr-2021, Body temperature: Concomitant product use was not provided by the reporter. Treatment information was not provided. Company comment: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. This is a case of product exposure during pregnancy with associated AEs for this 34-year-old female.; Reporter''s Comments: Since the nature of the reported reaction does imply seriousness according to one of the critera, the reaction was considered as serious by the Pharmacovigilance Centre. Sender''s Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. This is a case of product exposure during pregnancy with associated AEs for this 34-year-old female.


VAERS ID: 1452697 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-04-29
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: Patient has not had symptoms associated with COVID-19 Not had a COVID-19 test Patient is not enrolled in clinical trial
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021765065

Write-up: Miscarriage of pregnancy; This is a spontaneous report from a contactable consumer. This report is received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202106221233114910-Q16SV, Safety Report Unique Identifier is GB-MHRA-ADR 25520067. A female patient of an unspecified age received bnt162b2 (COVID-19 MRNA VACCINE BIONTECH, Solution for injection, Lot Number: Not reported), dose 2 via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient had not had symptoms associated with COVID-19, not had a COVID-19 test, and was not enrolled in any clinical trial. The patient previous vaccine included bnt162b2 (COVID-19 MRNA VACCINE BIONTECH, Solution for injection, Lot Number: Not reported), dose 1 via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunization. On 29Apr2021, the patient had a miscarriage of pregnancy. The outcome of the event was recovered with sequelae. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1660110 (history)  
Form: Version 2.0  
Age: 44.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-05
Onset:2021-04-29
   Days after vaccination:83
Submitted: 0000-00-00
Entered: 2021-08-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK4244 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Menstruation delayed, Ovulation delayed, Scan
SMQs:, Termination of pregnancy and risk of abortion (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID; LEVOTHYROXINE
Current Illness:
Preexisting Conditions: Comments: Patient has not had symptoms associated with COVID-19 Not had a COVID-19 test Patient is not currently breastfeeding
Allergies:
Diagnostic Lab Data: Test Name: Scan; Result Unstructured Data: Test Result:Baby was small
CDC Split Type: GBPFIZER INC202101064412

Write-up: Miscarried; Late period; Ovulation delayed; This is a spontaneous report from a contactable consumer (patient) received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202108161925229590-QUQPX, Safety Report Unique Identifier GB-MHRA-ADR 25806361. A 44-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EK4244), via an unspecified route of administration on 05Feb2021 (at the age of 44 years old) as dose 1, single for COVID-19 immunisation. The patient''s medical history was not reported. Patient has not had symptoms associated with COVID-19 and not had a COVID-19 test. Patient is not currently breastfeeding. Concomitant medications included folic acid taken for folic acid supplementation and levothyroxine from 01Mar2010. The patient miscarried on an unspecified date and late period and ovulation delayed on 29Apr2021. The mother reported she became pregnant while taking bnt162b2. The mother was 1 trimester pregnant at the onset of the event. The pregnancy resulted in spontaneous abortion. The patient underwent lab tests and procedures which included scan showed baby was small on an unspecified date. Outcome of the miscarried was unknown while of the remaining events was recovering. The clinical course was reported as follows: My periods are usually 28 days and I ovulate on day 11, since both my jabs my periods have been all over the place and so has my ovulation days. Patient has not tested positive for COVID-19 since having the vaccine. Patient is not enrolled in clinical trial. Did the medicine have an adverse effect on any aspect of the pregnancy: Yes. Pregnancy adverse effects details: Miscarried. Patient was exposed to the medicine first-trimester (1-12 weeks). Details of scans or investigations: Baby was small. No follow-up attempts are possible. No further information is expected.


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