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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

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Case Details (Sorted by Onset Date)

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VAERS ID: 1834322 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-27
Onset:2021-04-29
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-11-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed, Dizziness
SMQs:, Anticholinergic syndrome (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? No
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: Pregnancy
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC202101390975

Write-up: Missed Abortion; Dizziness; This is a spontaneous report from a non-contactable consumer downloaded from the Regulatory Authority-WEB DE-PEI-CADR2021173120, Safety Report Unique Identifier DE-PEI-202100180937. A 31-year-old female patient received bnt162b2 (COMIRNATY), via an unspecified route of administration on 27Apr2021 (Batch/Lot Number: Unknown) as dose number unknown, single for covid-19 immunisation. Medical history included pregnancy. The patient''s concomitant medications were not reported. The patient experienced dizziness on 29Apr2021 and missed abortion on 25May2021. The events caused hospitalization. Treatment of missed abortion was abrasion. The dizziness went away on its own. The patient became pregnant while taking bnt162b2. The patient was 2 months pregnant at the onset of the event. The patient underwent elective termination. The fetal outcome is intrauterine death. The outcome of the event dizziness was recovered on 30Apr2021 while missed abortion recovered on 13Jun2021. Sender Comment: Do you or the person concerned have any known allergies? If yes, which ones? No. Information on risk factors or previous illnesses. None / Treatment of Missed Abortion: Abrasion. The dizziness went away on its own. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1281477 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Georgia  
Vaccinated:2021-03-22
Onset:2021-04-30
   Days after vaccination:39
Submitted: 0000-00-00
Entered: 2021-05-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 030M20A / 1 - / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 023M20A / 2 - / -

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

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

Write-up: patient miscarried on 4/30/2021


VAERS ID: 1324105 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-07
Onset:2021-04-30
   Days after vaccination:23
Submitted: 0000-00-00
Entered: 2021-05-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 041A21A / N/A LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Chills, Exposure during pregnancy, Muscle spasms, Pyrexia, Ultrasound scan
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dystonia (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? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamins
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Ultrasound
CDC Split Type: vsafe

Write-up: When I got the vaccine, I had a fever, chills and cramps the day after the vaccine. It lasted for 30 hours. Three weeks after the vaccine I had a miscarriage at nine weeks gestation. I had some bleeding and I went to the doctors office between seven and eight weeks. I had chosen the J&J because it was not MNRA. Due Date-11/27/2021 Pregnancy-Third Pregnancy


VAERS ID: 1337095 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-23
Onset:2021-04-30
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-05-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 007C21A / 1 LA / SYR

Administered by: Private       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? Yes
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: I was 7 weeks pregnant at the time of receiving Dose 1 of the Moderna Covid vaccine. I began experiencing vaginal bleeding on Wednesday April 28. The bleeding continued and began heavier so I went to Urgent Care on Friday April 30. May 1 I experienced a miscarriage and lost the pregnancy.


VAERS ID: 1352052 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-10
Onset:2021-04-30
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-05-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW2239 / 2 LA / OT

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

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: FRPFIZER INC2021539255

Write-up: Pregnancy loss <20 weeks gestation/spontaneous miscarriage on 30Apr2021 at 8 amenorrhea weeks; This is a spontaneous report from a contactable physician downloaded from the FR-AFSSAPS-RS20211275, Safety Report Unique Identifier FR-AFSSAPS-2021050710. A 32-year-old female patient received bnt162b2 (COMIRNATY) dose 2 intramuscular administered in left arm on 10Apr2021 (Lot Number: EW2239) as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. No COVID disease history or COVID test. The patient was pregnant at time of vaccination. The patient experienced a spontaneous miscarriage on 30Apr2021 at 8 amenorrhea weeks, 20 days after D2(dose 2). The event was reported serious as medically significant and congenital anomaly. Date of last menstrual period was 05Mar2021. The mother was due to deliver on 10Dec2021. The outcome of event was recovered with sequel. No follow-up attempts are possible, no information is expected.


VAERS ID: 1393520 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-30
Onset:2021-04-30
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW2245 / 2 - / -

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

Life Threatening? No
Birth Defect? 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
Allergies:
Diagnostic Lab Data: Test Date: 20210522; Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test; Test Date: 20210521; Test Name: scan; Result Unstructured Data: Test Result:the baby had died
CDC Split Type: GBPFIZER INC2021620006

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer (patient) received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202105280646303010-GKWXK, Safety Report Unique Identifier GB-MHRA-ADR 25378095. A 35-year-old female patient received ,second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), at same age, via an unspecified route of administration on 30Apr2021 (Lot Number: EW2245) as 2ND DOSE, SINGLE DOSE for COVID-19 immunisation. Medical history included Lactation decreased and Folic acid supplementation. Patient no longer pregnant at the time of reporting. Concomitant medication included folic acid for vitamin supplementation. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Patient is pregnant at time of vaccination. The patient had the vaccine on the 30Apr2021 at 8 weeks 6 days pregnant. On the 21May2021 patient started bleeding, she went for a private scan and the baby had died, the baby measured at 8 weeks 6 days which would mean that it died on the day of the vaccine. Patient has not tested positive for COVID-19 since having the vaccine. The medicine had an adverse effect on aspect of the pregnancy and pregnancy adverse effect was miscarriage. Patient was exposed to the medicine first-trimester (1-12 weeks). The baby measured as 8 weeks and 6 days when it passed and this was the date patient had the vaccine. The patient underwent lab tests and procedures which included COVID-19 virus test: No - Negative COVID-19 test on 22May2021, ultrasound scan: the baby had died on 21May2021. The serious criteria was hospitalization prolonged. The outcome of event was recovering. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1546241 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2021-04-30
Onset:2021-04-30
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-08-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ET6956 / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Foetal cardiac arrest, Maternal exposure before pregnancy
SMQs:, Congenital and neonatal arrhythmias (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-07-01
   Days after onset: 62
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: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Allergies:
Diagnostic Lab Data:
CDC Split Type: FRPFIZER INC202100987903

Write-up: Foetal cardiac arrest; 30Apr2021, 2nd injection of bnt162b2, 11May2021, ovulation period, 21May2021, diagnosis of pregnancy.; This is a spontaneous report from a contactable consumer downloaded from the Regulatory Authority -WEB, regulatory authority number FR-AFSSAPS-NY20213048. This consumer reported information for both mother and fetal. This is a fetal report. Foetus patient without specified medical history. Concomitant medications were not reported. The patient''s mother received bnt162b2 (COMIRNATY, concentrate for injection. COVID-19 mRNA vaccine (modified nucleoside) (mRNA encoding the peak viral protein (S) of SARS-CoV-2), lot number ET6956) Intramuscularly administered in left arm on 30Apr2021 for Vaccination against covid-19. The fetus of an unspecified gender received the same vaccine transplacentally. On 01Jul2021, 63 Day after the last drug administration, the patient developed fetal cardiac arrest which led to death on 01Jul2021. Fetal cardiac arrest at 9 weeks of amenorrhea, 63 days after the second injection of the bnt162b2 vaccine by the mother. 30Apr2021, 2nd injection of bnt162b2, 11May2021, ovulation period, 21May2021, diagnosis of pregnancy. 01Jul2021, announces that the heart of the embryo has stopped. Miscarriage at 2 months of pregnancy. The event foetal cardiac arrest resulted in death. The patient diead on 01Jul2021. It was unknown if an autopsy was performed. The cause of death was foetal cardiac arrest. The outcome of foetal cardiac arrest was fatal. The outcome of other event was unknown. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : FR-PFIZER INC-202100988084 fetal/maternal case; Reported Cause(s) of Death: Foetal cardiac arrest


VAERS ID: 1724575 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-01
Onset:2021-04-30
   Days after vaccination:29
Submitted: 0000-00-00
Entered: 2021-09-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Clinical trial participant
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:no abnormalities; Comments: 12 week scan no problems noted
CDC Split Type: GBPFIZER INC202101182516

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer received from the regulatory authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202109081635562120-FFVAX. Safety Report Unique Identifier GB-MHRA-ADR 25913250. This consumer reported information for both mother and baby. This is a maternal report. A 35-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 01Apr2021 (Lot number was not reported) as dose 2, single for COVID-19 immunization. Medical history included clinical trial participant. The patient had normal pregnancies prior to miscarriages after having Pfizer vaccine. Patient has not had symptoms associated with COVID-19. Concomitant medication included folic acid taken for folic acid supplementation, start and stop date were not reported. The patient experienced miscarriage on 30Apr2021 with outcome of recovered on 30Apr2021. The patient underwent lab tests and procedures which included negative COVID-19 test on an unspecified date, 12 week scan and no abnormalities on an unspecified date no problems noted. Patient has not tested positive for COVID-19 since having the vaccine. Child was exposed to the medicine: first-trimester (1-12 weeks). No follow-up attempts are possible; Information about lot/batch number cannot be obtained.


VAERS ID: 1809188 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-07
Onset:2021-04-30
   Days after vaccination:23
Submitted: 0000-00-00
Entered: 2021-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain upper, Abortion missed, Body temperature, Endometritis, Haemorrhage in pregnancy, Human chorionic gonadotropin, Microbiology test, Pathology test, Pyrexia, Ultrasound scan
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? Yes
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: Abortion complete
Allergies:
Diagnostic Lab Data: Test Date: 202105; Test Name: fever; Result Unstructured Data: Test Result:fever; Test Date: 20210501; Test Name: bHCG; Result Unstructured Data: Test Result:70; Test Date: 202105; Test Name: Microbiology; Result Unstructured Data: Test Result:cultures pending; Test Date: 202105; Test Name: Pathology; Result Unstructured Data: Test Result:Results from fetal remains pending; Test Date: 20210501; Test Name: ultrasound; Result Unstructured Data: Test Result:incomplete abortion
CDC Split Type: ESPFIZER INC202101394868

Write-up: Abortion missed/incomplete abortion; Suspected post-curettage endometritiis; cramping pain in the epigastrium; Fever; great blood loss/major bleeding; This is a spontaneous report from a contactable consumer or other non hcp(patient) downloaded from the Agency Regulatory Authority -WEB, regulatory authority number ES-AEMPS-1027743. This is a mother report. A 45-years-old pregnant female patient received bnt162b2 (COMIRNATY, solution for injection, Lot Number: not reported) via an unspecified route of administration on 07Apr2021 as dose 2, single for covid-19 immunisation. Medical history included abortion complete on 25Feb2021, back pain from an unknown date and unknown if ongoing. The patient''s concomitant medications were not reported. The patient previously received dose 1 bnt162b2 (COMIRNATY, solution for injection, Lot Number: not reported ) via an unspecified route of administration on 17Mar2021 as dose 1, single for COVID-19 immunisation. The patient reported she became pregnant while taking bnt162b2. The mother was 12 Weeks pregnant at the onset of the event. The patient was due to deliver on 05Jan2022. Patient administered the second dose of pfizer without knowing that I was pregnant and against the background of a strong low back pain with which the vaccine coincided with other drugs. I suffered an abortion with great blood loss requiring blood transfusion. I was complicated by endometritis after curettage requiring intravenous antibiotics. Patient also had cramping pain in the epigastrium and Fever. Procedures include Ecoguided surgical curettage and Fetal remains are sent to Pathology and cultures to Microbiology. The Patient received treatment for the events. The outcome of the event Abortion missed was recovered on 05May2021, haemorrhage in pregnancy was recovered on unspecified date, endometritis was unknown and for all other events recovering. Discharge report: Refers after Last Menstrual Period 22Nov2020, a pregnancy with bleeding occurs in mid-Feb2021, the diagnosis of Deferred Abortion of 12 weeks; medical treatment is offered but the patient prefers to repeat the study in 1 week. Seen in the emergency room on 25Feb2021, due to new bleeding, complete abortion with regular Endrometical thickness of 14mm is checked ultrasound- Postabortion review is indicated on 30Mar2021. She doesn''t come because she was not bleeding. Last Menstrual Period normal postabortion: 31Mar2021, without contraceptive method. On day 30Apr2021, she has major bleeding again. She is diagnosed by ultrasound and bHCG (sub-unit beta human chorionic gonadotropin) of incomplete abortion (bHCG 70). It is treated with cytotec and surgical curettage. She hasn''t bled again. At 24-48h after curettage, she presents cramping pain in the epigastrium and fever. She is better. Suspected post-curettage endometritiis. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1281629 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-04-30
Onset:2021-05-01
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-05-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Chills, Dizziness, Dyspepsia, Exposure during pregnancy, Headache, Injection site pruritus, Injection site rash, Nausea, Pain, Pain in extremity, Paraesthesia, Pyrexia, Rash
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific dysfunction (narrow), 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), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

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

Write-up: Estimated due date of pregnancy was november 2021. We experienced a miscarriage during the vaccine symptoms of the first shot. The second dose of vaccine was way worse than the first. I got a sore arm, aches, a headache, nausea, a fever, chills, pins and needles feelings in my hands and feet, heartburn, and dizziness. I kept feeling like I might throw up and I developed a great big rash on my arm again, called covid arm. I spent the entire day on the couch next to a bucket because if I got up, I was too light headed and nauseated to do anything. It lasted 24 hours or so. By day 3 after the shot, I felt okay other than soreness, a headache, and a big itchy rash at the injection site. We are concerned about the miscarriage but don''t know if it was or wasn''t related to the vaccine. I did have a big reaction and we wonder if my immune system gearing up targeted the very early fetus as an intruder. We are deeply saddened by our loss.


VAERS ID: 1310363 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: South Dakota  
Vaccinated:2021-04-23
Onset:2021-05-01
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-05-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Full blood count, Human chorionic gonadotropin, Metabolic function test, Serum ferritin
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamin
Current Illness:
Preexisting Conditions:
Allergies: NKDA
Diagnostic Lab Data: 5/1/21 Hcg quant lab, 5/3 Hcg quant, ferritin, CBC, BMP labs
CDC Split Type:

Write-up: G2 P1 Patient with LMP of 4/2/21, EDD 1/7/21 received 2nd dose of covid vaccine and within a week experienced her first miscarriage. patient regrets getting vaccine and is upset/frustrated with the loss and concerned about future fertility


VAERS ID: 1322514 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: California  
Vaccinated:2021-05-01
Onset:2021-05-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamins, prenatal omegas, iron
Current Illness: None
Preexisting Conditions: Long-Covid asides that nothing
Allergies: None
Diagnostic Lab Data: Ultrasound 5/16
CDC Split Type:

Write-up: Fetal Death/ Intrauterine fetal death


VAERS ID: 1331444 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: California  
Vaccinated:2021-03-01
Onset:2021-05-01
   Days after vaccination:61
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 013A21A / 2 LA / 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? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamins
Current Illness: seasonal allergies
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: My doctor confirmed non-viable pregnancy in April and then I naturally miscarried in May.
CDC Split Type:

Write-up: I don''t believe this is due to the vaccine but I was still recommended to fill this out. I miscarried and my pregnancy ended in May. I got my first shot in February very early in my pregnancy when I wasn''t aware I was pregnant. I then proceeded the get my second shot which at that I knew I was maybe 6 weeks into pregnancy. I''ve never been pregnant before and the estimated date of delivery would have been November 2021.


VAERS ID: 1358535 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Maryland  
Vaccinated:2021-05-01
Onset:2021-05-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8731 / 1 LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: synthroid, prenatal vitamin
Current Illness: none
Preexisting Conditions: hashimoto''s disease
Allergies: none
Diagnostic Lab Data: I had a D&C on the Monday after the vaccine at the Hospital.
CDC Split Type: vsafe

Write-up: I did not feel adverse side effect, just sore arm. But there was bleeding that night, continuing that night and into Sunday. I went to my OB on Monday, I was 8 weeks and 4 days. They determined that the baby had stopped growing and there was no heartbeat and they declared it a miscarriage. Est due date was December 11 2021. No fever or any other side effects.


VAERS ID: 1378453 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2021-04-21
Onset:2021-05-01
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-06-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 030B21A / 2 RA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Human chorionic gonadotropin positive, Intermenstrual bleeding, Menstruation delayed, Pregnancy test positive, Ultrasound antenatal screen normal
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Tumour markers (narrow), 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? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: lexapro 10mg
Current Illness: none
Preexisting Conditions: anxiety
Allergies:
Diagnostic Lab Data: beta HCG tests - May 5 and May 7 Viability ultrasound - both abdominal and vaginal on May 10 pathology on gestational sac performed on May 12 - came back normal
CDC Split Type:

Write-up: after receiving vaccine on Wednesday 4/21, got positive pregnancy test on Saturday 4/24, 1 day after missed period. Estimated due date was 12/31/21. Began spotting on May 1 - approx 5 weeks pregnant. Spotted brown/pink with some clots until May 5, when I started lightly bleeding red. Beta tests on May 5 and May 7 showed 6228.7 and 6529.0, respectively. May 10 went in for viability scan - ultrasound showed gestational sac with 2 yolk sacs and 2 fetal poles, one measuring at 6 weeks and other measuring at 6w1d. No sign of misscarriage, no reason for bleeding was seen on the scan. Scan was perfect on paper. Bleeding picked up after scan and I lost the pregnancy on May 11 around 4:30pm. Bleeding continued for one week and HCG levels were low enough to show a negative test at my followup appointment 2 weeks later on May 26.


VAERS ID: 1412054 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-02-26
Onset:2021-05-01
   Days after vaccination:64
Submitted: 0000-00-00
Entered: 2021-06-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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: Became pregnant within a month of receiving vaccine. Miscarried at 6 weeks


VAERS ID: 1416524 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: California  
Vaccinated:2021-05-03
Onset:2021-05-01
Submitted: 0000-00-00
Entered: 2021-06-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8735 / 2 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion missed, Fatigue, Pain in extremity, Ultrasound foetal
SMQs:, Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Allergies:
Diagnostic Lab Data: Test Name: ultrasound; Result Unstructured Data: Test Result:the growth stopped/no heartbeat; Comments: She declared it missed abortion
CDC Split Type: USPFIZER INC2021664318

Write-up: My pregnancy symptom s started disappearing gradually and after a week I didn''t feel pregnant at all/missed abortion; My arm was sore; I felt mild fatigue; This is spontaneous report from contactable consumer. A 28 year-old female consumer (patient) reported that received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number ER8735), on 03May2021 (at the age of 28-years-old) at single dose for COVID-19 immunization. The patient had received the first dose of vaccine on 13Apr2021 (lot EW0164). The patient had no known allergies and had not other medical history. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient reported that she got her 2nd dose of vaccination when she was 7 weeks pregnant. The LMP was on 21Mar2021. Her arm was sore and she felt mild fatigue. Her pregnancy symptoms started disappearing gradually and after a week she didn''t feel pregnant at all. When she went in for her first ultrasound appointment at 9 weeks, the doctor said that the growth stopped at 7 weeks 4 days and there was no heartbeat. She declared it missed abortion. Information on Lot/Batch number was available. Additional information has been requested.


VAERS ID: 1430550 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Maine  
Vaccinated:2021-04-07
Onset:2021-05-01
   Days after vaccination:24
Submitted: 0000-00-00
Entered: 2021-06-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / -

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

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Multi vitamin
Current Illness: N/a
Preexisting Conditions: N/a
Allergies:
Diagnostic Lab Data: D & E - 18 weeks
CDC Split Type:

Write-up: Loss of pregnancy at 15 weeks


VAERS ID: 1496142 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Louisiana  
Vaccinated:2020-12-01
Onset:2021-05-01
   Days after vaccination:151
Submitted: 0000-00-00
Entered: 2021-07-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3246 / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion missed, Maternal exposure before pregnancy, Pregnancy, Pregnancy test urine positive, Ultrasound scan abnormal, Uterine dilation and curettage
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), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Pre-natal vitamin with 200 mg DHA
Current Illness: None
Preexisting Conditions: Hypoglycemia
Allergies: NKDA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pregnancy on 4/1/21. Pregnancy confirmation ultrasound on 5/13/21 showed missed abortion. D&C performed 5/14/21.


VAERS ID: 1536031 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-04-27
Onset:2021-05-01
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-08-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Ultrasound abdomen
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: April 27th covid 9 moderna vaccination May 1st bleeding- rhogam shot and ultrasound May 6th ultrasound May 13th ultrasound May 27th ultrasound - no pregnancy
CDC Split Type:

Write-up: March 24th was the last first day of my period, became pregnant. Received my first covid 9 vaccine moderna on April 27th. Noticed bleeding on May 1st morning. Went into hospital and received rhogam shot and went for ultrasound same day. Pregnancy was still there and went for another ultrasound the following week. A heartbeat was detected and sizing was accurate for gestation period. May 13th was my 3rd ultrasound and when they noticed the decreased heartrate and the lack of growth. I miscarried on May 19th. Went for my last ultrasound on May 27th when they determined that my pregnancy was no longer there.


VAERS ID: 1628830 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Hawaii  
Vaccinated:2021-04-21
Onset:2021-05-01
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-08-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0158 / 1 LA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0173 / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Blood pressure increased, Caesarean section, Exposure during pregnancy, Gestational hypertension, Pre-eclampsia, Premature delivery
SMQs:, Neuroleptic malignant syndrome (broad), Hypertension (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 7 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: Sulpha drugs
Diagnostic Lab Data: Blood pressure measurements Metabolic profile 24 urine test positive for protein in urine NST
CDC Split Type:

Write-up: Gestational hypertension in third trimester developing into severe preeclampsia, blood pressure climbed in the weeks before delivery and reached max of approximately 180/110 First pregnancy Baby was breech, delivered by c-section one day short of 37 weeks, birth weight 6 lb 0.05 oz Baby with very minor hypospadias and hydrocele in testicle, otherwise healthy


VAERS ID: 1727520 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Maine  
Vaccinated:2021-05-01
Onset:2021-05-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-09-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8634 / 2 - / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: First dose, rash on arm if injection, flu like symptoms
Other Medications: Wellbutrin
Current Illness: None reported
Preexisting Conditions: Pituitary tumor, celiac
Allergies: Gluten, egg, raspberry, mango
Diagnostic Lab Data: Ultrasound 7/6 showing miscarriage after healthy pregnancy
CDC Split Type:

Write-up: Miscarriage, rash covering neck and chest, fever, tiredness


VAERS ID: 1750459 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Guam  
Vaccinated:2020-12-21
Onset:2021-05-01
   Days after vaccination:131
Submitted: 0000-00-00
Entered: 2021-09-30
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 / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Human chorionic gonadotropin negative, Maternal exposure before pregnancy, Ultrasound scan normal
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: Lisinopril / Carvedilol
Current Illness: N/A
Preexisting Conditions: Hypertension
Allergies: N/A
Diagnostic Lab Data: Ultrasound and Beta HCG confirmation of miscarriage done.
CDC Split Type:

Write-up: Miscarriage, May 2021 LMP, 03/01/2021


VAERS ID: 1750474 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Guam  
Vaccinated:2021-03-25
Onset:2021-05-01
   Days after vaccination:37
Submitted: 0000-00-00
Entered: 2021-09-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM6204 / 1 AR / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8729 / 2 AR / IM

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

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

Write-up: LMP, 03/02/2021 Miscarriage, 05/2021


VAERS ID: 1752844 (history)  
Form: Version 2.0  
Age: 23.0  
Sex: Female  
Location: Guam  
Vaccinated:2021-04-17
Onset:2021-05-01
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-10-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA ER8729 / 1 RA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA ER8729 / 2 RA / IM

Administered by: School       Purchased by: ?
Symptoms: Abortion spontaneous, Emotional distress, First trimester pregnancy, General physical condition abnormal, Pregnancy test negative, Ultrasound scan abnormal
SMQs:, Malignancy related therapeutic and diagnostic procedures (narrow), Depression (excl suicide and self injury) (broad), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: First trimester miscarriage confirmed post vaccine by ultrasound and Beta HCG. Patient is recovering from physical and emotional trauma. Will continue to follow.
CDC Split Type:

Write-up: Miscarriage on 05/2021.


VAERS ID: 1356442 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-28
Onset:2021-05-01
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-05-28
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 INC2021539958

Write-up: My fiance had the first COVID19 jab on 28th April and 2 weeks later she had a miscarriage.; This is a spontaneous report from a contactable consumer. A 27-year-old pregnant female patient received the first dose of BNT162B2 (Lot number was not reported), via an unspecified route of administration on 28Apr2021 as single dose for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. The patient''s fiance had the first covid19 jab on 28th April and 2 weeks in May2021 later she had a miscarriage. The outcome of the event was unknown. Information on the lot/batch number has been requested.


VAERS ID: 1374562 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-09
Onset:2021-05-01
   Days after vaccination:22
Submitted: 0000-00-00
Entered: 2021-06-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW2239 / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion induced, Foetal death, 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? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Hashimoto''s disease; Pollinosis (Grass pollen allergy)
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: pregnancy test; Result Unstructured Data: Test Result:positive; Comments: Test carried out only after vaccination.; Test Date: 20210510; Test Name: Ultrasound; Result Unstructured Data: Test Result:heartbeat could not be detected; Comments: At 10 weeks
CDC Split Type: ATPFIZER INC2021579451

Write-up: Determination of the miscarriage on 10May / No heartbeat could be seen on the ultrasound at 10 weeks of gestation; Abortion induced; This is a spontaneous report from a contactable consumer downloaded from the WEB [AT-BASGAGES-2021-27203]. A 35-year-old pregnant female patient received bnt162b2 (COMIRNATY, Lot Number: EW2239), intramuscular on 09Apr2021 as 1st dose, 0.3 ml single for COVID-19 immunization. The patient''s medical history included pollinosis (Grass pollen allergy) and Hashimoto''s disease, both were ongoing. The patient''s concomitant medications were not reported. On 10May2021 the patient experienced fetal death in utero. On unspecified date in May2021 the patient experienced abortion induced. The patient explained that she did not yet know she was pregnant at the time of the vaccination. A positive pregnancy test was only carried out after the vaccination on unspecified date. In the 10th week of pregnancy (10May2021), a heartbeat could not be detected with ultrasound, therefore an abortion was carried out. The patient stated that the doctors do not see the link to the vaccination, so that an incident happens relatively often. They have, however, requested that the patient makes this report as they could not rule it out completely. The outcome of the event fetal death in utero was unknown and the remaining events recovered on unspecified date. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1393079 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-14
Onset:2021-05-01
Submitted: 0000-00-00
Entered: 2021-06-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ET8885 / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021619942

Write-up: Maternal exposure during pregnancy/6.5 weeks pregnant; Early miscarriage; This is a spontaneous report from a contactable consumer (patient) received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-ADR 25365378, Safety Report Unique Identifier GB-MHRA-ADR 25365378. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 14May2021 (Batch/Lot Number: ET8885) as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced early miscarriage (medically significant) on an unspecified date in May2021 with outcome of unknown, maternal exposure during pregnancy(medically significant) on an unspecified date in May2021 with outcome of unknown. Patient didn''t know if it''s related or not but sadly she had a miscarriage the day after Pfizer vaccine. She was 6.5 weeks pregnant. She felt that she should flag this up. She has attached a photograph of vaccine certificate. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1400706 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-06
Onset:2021-05-01
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-06-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW2239 / 1 LA / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Intrauterine contraception (Wore an IUD for 2 years); Miscarriage (1st miscarriage)
Allergies:
Diagnostic Lab Data: Test Name: thrombophilia check-up; Result Unstructured Data: Test Result:unknown results
CDC Split Type: FRPFIZER INC2021628360

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer downloaded from a regulatory authority-WEB, regulatory authority number is FR-AFSSAPS-2021053869. A 34-year-old pregnant female patient received BNT162B2 (COMIRNATY, solution for injection), dose 1 intramuscular, administered in arm left on 06Apr2021 (Batch/Lot Number: EW2239) (at the age of 34-years-old) as 1st dose, single dose for COVID-19 immunisation. Medical history included first miscarriage in Sep2020 and wore an IUD (intrauterine device) for 2 years. The patient''s concomitant medications were not reported. The patient had good tolerance on the first dose: no fever and no flu syndrome. On 01May2021, miscarriage occurred at 1 month of pregnancy (also reported as Day +26). A check-up is in progress to look for possible etiologies for these two miscarriages (including thrombophilia check-up). The reporter assessed the event as serious (medically significant). Outcome of the event was recovering. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1400925 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-11
Onset:2021-05-01
Submitted: 0000-00-00
Entered: 2021-06-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW4109 / 1 - / -

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

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: Patient has not had symptoms associated with COVID-19 Patient is not enrolled in clinical trial
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test; Test Name: Ultrasound; Result Unstructured Data: Test Result:unknown
CDC Split Type: GBPFIZER INC2021633350

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer received from a regulatory authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202105311717472110-YVNWO. Safety Report Unique Identifier GB-MHRA-ADR 25393679. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) dose 1 via an unspecified route of administration on 11May2021 (lot number: Ew4109; expiry date: unknown) as 1st dose, single, for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient experienced miscarriage on an unspecified date in May2021. Additional information: Had the vaccine at 7 weeks 5 days; baby stopped growing at 8 weeks. The events were considered serious due to other medically important condition and congenital anomaly. The patient underwent lab tests and procedures which included COVID-19 virus test: no - negative on unspecified date; and ultrasound: unknown on unspecified date. Patient has not tested positive for COVID-19 since having the vaccine. Outcome of the event was recovering. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1412169 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-01
Onset:2021-05-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EX 6537 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Blood pressure measurement, Chills, Foetal death, Liver function test, Pre-eclampsia, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Hypertension (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? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: TROMBYL
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Stroke (without sequele)
Allergies:
Diagnostic Lab Data: Test Date: 2021; Test Name: BP; Result Unstructured Data: Test Result:increased; Comments: diagnosis preeclampsia; Test Date: 2021; Test Name: BP; Result Unstructured Data: Test Result:nomalized; Comments: Postpartum; Test Date: 2021; Test Name: liver test; Result Unstructured Data: Test Result:liver effects; Comments: diagnosis preeclampsia; Test Date: 2021; Test Name: liver test; Result Unstructured Data: Test Result:normalized; Comments: Postpartum
CDC Split Type: SEPFIZER INC2021653542

Write-up: Death intrauterine; Preeclampsia; chills; fever; This is a spontaneous report from a contactable physician downloaded from a regulatory authority-WEB SE-MPA-2021-044382. A 38-year-old female patient received the 1st dose of BNT162b2 (COMIRNATY), via an unspecified route of administration in May2021 (Batch/Lot Number: EX 6537) as single dose for Covid-19 immunization. Medical history included stroke in 2016 without sequele. Concomitant medications included acetylsalicylic acid (TROMBYL) taken for an unspecified indication from 09Nov2020 to May2021. Reported suspected adverse event was intrauterine foetal death. On vaccination day the patient was pregnant in week 32 + 2. Some days after the vaccine she got a fever and chills that she recovered from after a few days. Felt normal fetal movements the next few days. Nine days after vaccination, she began to feel altered fetal movements, she sought care. Pregnant in week 34 + 4. Intrauterine fetal death was found by the health care. The next day, childbirth was induced. On this day, the patient developed increased blood pressure and liver effects, diagnosis preeclampsia. Childbirth after another day. The placenta and baby were inspected, no obvious abnormality was seen. Samples taken, placenta sent for pathological anatomical diagnosis and the child will be autopsied, answers not yet available. Postpartum, the patient''s blood pressure and liver samples were normalized (as reported). The reporter wondered if affected liver samples had something to do with the vaccine. Reporter writes: Microthrombosis? Patient was physically well. The outcome of events chills and fever was recovered in 2021. The outcome of events intrauterine foetal death and preeclampsia was recovering. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1438401 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-01
Onset:2021-05-01
   Days after vaccination:61
Submitted: 0000-00-00
Entered: 2021-06-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: FRPFIZER INC2021713450

Write-up: During periconceptional period, a miscarriage occurred after the first dose of vaccine; During periconceptional period, a miscarriage occurred after the first dose of vaccine; This is a spontaneous report from a contactable other healthcare professional via Medical Information. A 27-year-old pregnant female patient received BNT162b2 (COMIRNATY, Solution for injection, Lot number- unknown) during periconceptional period via an unspecified route of administration in Mar2021 (either on 30Mar2021 or on 31Mar2021) as dose 1 single for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient was not sure about the exact date. In the end of May2021 (after the first dose of vaccine), the patient experienced a miscarriage. It had been over 2 months, that the patient did not get her second dose of vaccine. So, the reporter asked if the patient must receive the second dose of vaccine. Then the reporter asked if the patient should receive a dose of JANSSEN vaccine. The reporter also asked if it was useful to do a serology test. The outcome of the events was unknown.; Sender''s Comments: A causal association between BNT162B2 and the reported miscarriage with exposure during pregnancy cannot be completely excluded based on information provided. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1468257 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-14
Onset:2021-05-01
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-07-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EX0893 / 1 - / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: FRPFIZER INC2021795794

Write-up: Pregnancy loss <20 weeks gestation; This is a spontaneous report from a contactable healthcare professional downloaded from the WEB with regulatory authority report number FR-AFSSAPS-RN20211664 and Safety Report Unique Identifier FR-AFSSAPS-2021067425. A 28-year-old female patient received dose 1 of BNT162B2 (COMIRNATY; lot number EX0893) intramuscularly on 14Apr2021 as a single dose for COVID-19 immunization. The patient had no documented history. The patient was 6 weeks pregnant at the time of vaccination. Concomitant medications were not reported. On 01May2021, the patient experienced pregnancy loss at < 20 weeks. The patient had a miscarriage. The outcome of pregnancy loss was recovered with sequelae. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1488561 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Male  
Location: Foreign  
Vaccinated:2021-01-01
Onset:2021-05-01
   Days after vaccination:120
Submitted: 0000-00-00
Entered: 2021-07-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 - / OT

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

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-06-01
   Days after onset: 31
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: No medical history was provided.
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBMODERNATX, INC.MOD20212

Write-up: Fetal death; This regulatory authority case was reported by a consumer and describes the occurrence of FOETAL DEATH (Fetal death) in a 26-year-old male patient who received mRNA-1273 (Moderna CoviD-19 Vaccine) for COVID-19 vaccination. No medical history was provided. On 01-Jan-2021, the patient received second dose of mRNA-1273 (Moderna CoviD-19 Vaccine) (Intramuscular) 1 dosage form. On 01-May-2021, after starting mRNA-1273 (Moderna CoviD-19 Vaccine), the patient experienced FOETAL DEATH (Fetal death) (seriousness criteria death and medically significant). The patient died on 01-Jun-2021. The cause of death was not reported. It is unknown if an autopsy was performed. Concomitant medications were not reported. Treatment details were not provided. This is a case of Fetal death in a 26-year-old reported as male patient (unable to confirm patient gender), 120 days after receiving second dose of vaccine (Lot number unknown). Very limited information regarding the clinical details pertaining to the fetal death in terms of gestational age at the time of vaccination and death, and the unconfirmed patient''s gender was provided at this time. No further information is expected.; Sender''s Comments: This is a case of Fetal death in a 26-year-old reported as male patient (unable to confirm patient gender), 120 days after receiving second dose of vaccine (Lot number unknown). Very limited information regarding the clinical details pertaining to the fetal death in terms of gestational age at the time of vaccination and death, and the unconfirmed patient''s gender was provided at this time. No further information is expected.; Reported Cause(s) of Death: unknown cause of death


VAERS ID: 1538279 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-19
Onset:2021-05-01
Submitted: 0000-00-00
Entered: 2021-08-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ET8885 L658 / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: OMEPRAZOL; YASMIN
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Lactation decreased; Miscarriage; Oesophageal acid reflux; Pregnancy
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test; Test Date: 202105; Test Name: Scan; Result Unstructured Data: Test Result:showed miscarriage had taken place and that tissue; Comments: showed miscarriage had taken place and that tissue was left inside
CDC Split Type: GBPFIZER INC202100943146

Write-up: Miscarriage of pregnancy; bleeding; pregnant; This is a spontaneous report from a contactable consumer (patient) received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202107240137457010-WRCPV, Safety Report Unique Identifier GB-MHRA-ADR 25702274. A 25-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) dose 1 via an unspecified route of administration on 19May2021 (Lot Number: ET8885 L658) as single dose for COVID-19 immunisation. Medical history included lactation decreased, miscarriage, pregnancy, oesophageal acid reflux. Patient had not had symptoms associated with COVID-19. Patient was not currently breastfeeding. Patient was not enrolled in clinical trial. Concomitant medications included omeprazole (OMEPRAZOL) taken for oesophageal acid reflux; drospirenone, ethinylestradiol (YASMIN). The patient previously took folic acid. The patient experienced miscarriage of pregnancy on 22May2021 with outcome of recovered on 28May2021, bleeding in May2021 and pregnant in 2021 both with outcome of recovering. Clinical course: When patient had the vaccine, she did not know she was approximately 8 weeks pregnant. A few days later, she started bleeding and got admitted to hospital where she found out she was pregnant and miscarrying. Patient did not take folic acid supplement during pregnancy. Patient was hospitalized from 24May2021 with miscarriage. Patient was exposed to the medicine first-trimester (1-12 weeks). Scan showed miscarriage had taken place and that tissue was left inside in May2021. The patient underwent lab tests and procedures which included sars-cov-2 test: no - negative covid-19 test on an unspecified date. Patient had not tested positive for COVID-19 since having the vaccine. No Follow-up attempts are needed. No further information is expected.


VAERS ID: 1680618 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-16
Onset:2021-05-01
Submitted: 0000-00-00
Entered: 2021-09-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Arthralgia, Asthenia, Dysmenorrhoea, Fatigue, Gait disturbance, Heavy menstrual bleeding, Maternal exposure during pregnancy, Menstruation irregular, Ovarian cyst, Pain in extremity, Somnolence, Visual impairment
SMQs:, Peripheral neuropathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Glaucoma (broad), Optic nerve disorders (broad), Lens disorders (broad), Retinal disorders (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: HUPFIZER INC202101097056

Write-up: my vision has deteriorated significantly; I started bleeding again, blood was pouring out of me again for 4 days; a cyst in my left ovary; gestational sac with an embryo node; menstruation differently than usual with huge quantities; menstruation differently than usual with even stronger cramps than before; completely weakened; my left thigh started to hurt terribly; my knee also hurts a lot; I can barely walk; I was no longer pregnant; sudden feeling of tiredness, exhaustion; fell asleep; This is a spontaneous report from a contactable consumer (patient). This consumer reported events after two vaccine doses. This is the first of two reports. A female patient of an unspecified age received bnt162b2 (COMIRNATY) via an unspecified route of administration on 16May2021 (Batch/Lot number was not reported) as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The consumer reported that her menstruation came on time that day (16May2021), but differently than usual with huge quantities and with even stronger cramps than before. The blood flowed from her for 4 days, she was completely weakened. From unknown date, she had sudden feeling of tiredness, exhaustion anywhere, anytime for about 3 weeks. From one moment to the next she fell asleep, she did not dare to drive, to work. On 20May2021, she visited the gynecologist for plentiful bleeding, who then found a cyst in her left ovary, as well as a gestational sac with an embryo node. On 28May2021, she went to the gynecologist again because she felt that there was a problem, of course she was no longer pregnant. On 29May2021 she started bleeding again, blood was pouring out of her again for 4 days. A few days after the vaccination her left thigh started to hurt terribly, which has not passed since and many times her knee also hurts a lot, she can barely walk! Her vision has deteriorated significantly, although she had not been to an ophthalmologist yet. The outcome of tiredness/ exhaustion and fell asleep was recovered, of left thigh hurt, knee hurts a lot and can barely walk was not recovered, of others was unknown. Information on batch/lot number will be requested in follow-up.


VAERS ID: 1730846 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-23
Onset:2021-05-01
Submitted: 0000-00-00
Entered: 2021-09-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Breast pain, Constipation, Decreased appetite, Heavy menstrual bleeding, Inappropriate schedule of product administration, Influenza, Injection site erythema, Menstruation irregular, Myalgia, SARS-CoV-2 test, Somatic symptom disorder of pregnancy, Weight decreased
SMQs:, Rhabdomyolysis/myopathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Lipodystrophy (broad), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (broad), Tendinopathies and ligament disorders (broad), Medication errors (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: COVID-19 test
CDC Split Type: GBMODERNATX, INC.MOD20213

Write-up: miscarriage; My periods have been early; pain and sore boobs; Constipated; achy body; Phantom pregnancy; Inappropriate schedule of vaccine administered; Flu symptoms; Heavy periods; Weight loss; Appetite lost; red ring around the injection site; This case was received via Regulatory Authority (Reference number: GB-MHRA-ADR 25951612) on 17-Sep-2021 and was forwarded to Moderna on 17-Sep-2021. This regulatory authority case was reported by a consumer and describes the occurrence of HEAVY MENSTRUAL BLEEDING (Heavy periods), ABORTION SPONTANEOUS (miscarriage), SOMATIC SYMPTOM DISORDER OF PREGNANCY (Phantom pregnancy), WEIGHT DECREASED (Weight loss), DECREASED APPETITE (Appetite lost) and INFLUENZA (Flu symptoms) in a 34-year-old female patient who received mRNA-1273 (Moderna CoviD-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 23-May-2021, the patient received first dose of mRNA-1273 (Moderna CoviD-19 Vaccine) (unknown route) 1 dosage form. On 08-Aug-2021, received second dose of mRNA-1273 (Moderna CoviD-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In May 2021, the patient experienced INJECTION SITE ERYTHEMA (red ring around the injection site). On 23-May-2021, the patient experienced WEIGHT DECREASED (Weight loss) (seriousness criteria disability and medically significant) and DECREASED APPETITE (Appetite lost) (seriousness criteria disability and medically significant). On 28-May-2021, the patient experienced HEAVY MENSTRUAL BLEEDING (Heavy periods) (seriousness criteria disability and medically significant). On 08-Aug-2021, the patient experienced INFLUENZA (Flu symptoms) (seriousness criteria disability and medically significant). 08-Aug-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). On 18-Aug-2021, the patient experienced SOMATIC SYMPTOM DISORDER OF PREGNANCY (Phantom pregnancy) (seriousness criteria disability and medically significant). On an unknown date, the patient experienced ABORTION SPONTANEOUS (miscarriage) (seriousness criteria disability and medically significant), MENSTRUATION IRREGULAR (My periods have been early), BREAST PAIN (pain and sore boobs), CONSTIPATION (Constipated) and MYALGIA (achy body). On 16-Jun-2021, DECREASED APPETITE (Appetite lost) had resolved. On 18-Jun-2021, WEIGHT DECREASED (Weight loss) had resolved. On 08-Aug-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. On 11-Aug-2021, INFLUENZA (Flu symptoms) had resolved. On 11-Sep-2021, SOMATIC SYMPTOM DISORDER OF PREGNANCY (Phantom pregnancy) had resolved. At the time of the report, HEAVY MENSTRUAL BLEEDING (Heavy periods) had not resolved, ABORTION SPONTANEOUS (miscarriage) and INJECTION SITE ERYTHEMA (red ring around the injection site) had resolved and MENSTRUATION IRREGULAR (My periods have been early), BREAST PAIN (pain and sore boobs), CONSTIPATION (Constipated) and MYALGIA (achy body) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: no (Negative) COVID-19 test. The action taken with mRNA-1273 (Moderna CoviD-19 Vaccine) (Unknown) was unknown. Patient reported that she experienced lost her appetite, red ring around the injection site, fidgety and periods have been early, heavier and she had pain and sore boobs. Patient has not had symptoms associated with COVID-19 Patient is not pregnant,Patient is not currently breastfeeding Concomitant product was not provided. Treatment medication was not reported. This case concerns a 34-year-old female patient with no relevant history reported, who experienced the serious unexpected events Heavy menstrual bleeding, weight decreased and non-serious events menstruation irregular and breast pain. The events occurred after the first dose and after the second and most recent dose of mRNA-1273 Moderna vaccine. Events seriousness (disabling and MS) captured as per Regulatory Authority assessment in Source Document. Also as serious events were captured Miscarriage and Phantom pregnancy from the verbatim: "But prior to this i thought i was pregnant? believe this was either a phantom pregnancy or miscarriage". No causality assessment was provided by the reporter. The benefit-risk relationship of mRNA-1273 Moderna vaccine is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 21-Sep-2021: Follow-up received on 21-Sep-2021 and does not contain any new information.; Sender''s Comments: This case concerns a 34-year-old female patient with no relevant history reported, who experienced the serious unexpected events Heavy menstrual bleeding, weight decreased and non-serious events menstruation irregular and breast pain. The events occurred after the first dose and after the second and most recent dose of mRNA-1273 Moderna vaccine. Events seriousness (disabling and MS) captured as per Regulatory Authority assessment in Source Document. Also as serious events were captured Miscarriage and Phantom pregnancy from the verbatim: "But prior to this i thought i was pregnant? believe this was either a phantom pregnancy or miscarriage". No causality assessment was provided by the reporter. The benefit-risk relationship of mRNA-1273 Moderna vaccine is not affected by this report.


VAERS ID: 1769668 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-01
Onset:2021-05-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-10-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test; Comments: Negative COVID-19 test.
CDC Split Type: GBPFIZER INC202101266291

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-202109251011531660-AZKAO. Safety Report Unique Identifier GB-MHRA-ADR 25994724. This consumer reported information for mother. This is a {maternal} report. A 31-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) via an unspecified route of administration on May2021 (Batch/Lot number: not reported) as dose 1, single for COVID-19 immunization. The patient received 2nd dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on Jul2021 (Lot/Batch no. Unknown). Medical history and concomitant medications were not reported. Patient had no symptoms associated with COVID-19. Patient had not tested positive for COVID-19 since having the vaccine. Patient was not enrolled in clinical trial. The patient experienced miscarriage (medically significant) on May2021. The patient reported she became pregnant while taking bnt162b2. Three days after her first vaccine she had a very early miscarriage. The patient underwent lab tests and procedures which included sars-cov-2 test: no - negative covid-19 test- Negative COVID-19 test on an unspecified date. The outcome of event was recovered on May2021. No follow-up attempts are possible, Information about Batch/Lot Number cannot be obtained. No further information is expected.


VAERS ID: 1326568 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-04-27
Onset:2021-05-02
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-05-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0171 / 1 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: we have no information about gestational age or if patient sought treatment for miscarriage. we have no information about miscarriage other than verbal report
CDC Split Type:

Write-up: patient came in 5/18/21 for her second dose that informed me that she miscarried 5 days after receiving her first dose of the Pfizer vaccine on 4/27/21.


VAERS ID: 1394758 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: New York  
Vaccinated:2021-04-16
Onset:2021-05-02
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-06-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Malaise, Rash, Rash erythematous, Uterine dilation and curettage
SMQs:, Anaphylactic reaction (broad), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? 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: I had to have a D and C
CDC Split Type:

Write-up: Had a horrible red rash down my left arm and felt sick for several days then I miscarried.


VAERS ID: 1338975 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-05-02
Submitted: 0000-00-00
Entered: 2021-05-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Computerised tomogram, Cough, Foetal heart rate abnormal, Foetal hypokinesia, Headache, Maternal exposure during pregnancy, Oropharyngeal pain, SARS-CoV-2 test
SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (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), 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: Cough; Lactation decreased; Pregnancy (Patient no longer pregnant at the time of reporting.); Sore throat; Vitamin supplementation
Allergies:
Diagnostic Lab Data: Test Name: scans; Result Unstructured Data: Test Result:missed/silent miscarriage; Test Date: 20210505; Test Name: COVID-19 virus test; Test Result: Negative
CDC Split Type: GBPFIZER INC2021516616

Write-up: fetal growth; missed/silent miscarriage; Maternal exposure during pregnancy; Then scans showed no heartbeat; headache; sore throat; cough; Early miscarriage; This is a spontaneous report from a contactable consumer. This is a report received from the Regulatory Agency. Regulatory authority report number GB-MHRA-WEBCOVID-202105082255250640-AQDPH, Safety Report Unique Identifier GB-MHRA-ADR 25267210. The 22-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) via an unspecified route of administration at single dose on an unspecified date as an unspecified dose for COVID-19 immunisation; covid-19 vaccine (COVID-19 VACCINE ASTRAZENECA), route of administration, start and stop date, batch/lot number and dose were not reported for an unspecified indication. Medical history included suppressed lactation, oropharyngeal pain, cough, oropharyngeal pain, cough from an unknown date and unknown if ongoing, pregnancy from an unknown date and unknown if ongoing Patient no longer pregnant at the time of reporting, vitamin supplementation. Concomitant medication(s) included folic acid (FOLIC ACID) taken for vitamin supplementation. The patient was extremely healthy and take no medication Patient had no symptoms associated with COVID-19 Patient is not enrolled in clinical trial Patient is not currently breastfeeding. The patient''s Pregnancy was progressing normally. she went for a scan exactly one week after spending 5 hours with vaccinated neighbours. The scan showed the growth to be at 6 weeks 1 day, which was a week behind her pregnancy in weeks according to conception date. Follow up scans confirmed the missed/silent miscarriage. 48 hours after being with my neighbours, the patient began to feel unwell with a headache that became severe and lasted 8 days. The patient also developed a sore throat and cough. During this time my pregnancy stopped developing as well (as confirmed by growth measurements on scans and explained above). The medicine have an adverse effect on any aspect of the pregnancy was yes. Pregnancy adverse effects details was Missed miscarriage following exposure to vaccinated people. Details of previous pregnancies included previous pregnancy was healthy and successful. Her three scans to confirm miscarriage showed growth to be 6 weeks- matches exactly the time, she spent 5 hours around vaccinated people after which - severe headache, sore throat and loss of heartbeat. Patient was exposed to the medicine first-trimester (1-12 weeks). Details of scans or investigations included All was going well, healthy second pregnancy, Then scans showed no heartbeat and foetal growth had stopped two weeks prior. The patient underwent lab tests and procedures which included computerised tomogram: missed/silent miscarriage on, sars-cov-2 test: negative on 05May2021. The outcome of the event fetal growth missed miscarriage, headache, sore throat, cough, maternal exposure during pregnancy was unknown and early miscarriage was not recovered on. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1352780 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-06
Onset:2021-05-03
   Days after vaccination:27
Submitted: 0000-00-00
Entered: 2021-05-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 45A21A / 1 RA / IM

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

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

Write-up: Stillbirth at 39 weeks and 3 days


VAERS ID: 1371988 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-04-30
Onset:2021-05-03
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-06-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 017C21A / 2 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound scan, Uterine dilation and curettage
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: Pre-natal Vitamin
Current Illness: No known
Preexisting Conditions: Psoraisis
Allergies: No known
Diagnostic Lab Data: Medically managed miscarriage and subsequent D&C procedure
CDC Split Type:

Write-up: Loss of pregnancy. I received my first dose at approximately 4 weeks pregnant on 3/30. I had a positive home pregnancy test the following day on 3/31. On 4.29, I had my first confirmation ultrasound where a heartbeat was found, but the fetus was not measuring as expected. On 4.30, I received my 2nd dose of the Moderna vaccine. A follow-up ultrasound was done on 4.12, at that time, no heartbeat was indicated and the fetus had stopped developing shortly after receiving the 2nd does on 4.30. This was my first pregnancy.


VAERS ID: 1523085 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-27
Onset:2021-05-03
   Days after vaccination:65
Submitted: 0000-00-00
Entered: 2021-08-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 023M20A / UNK LA / IM

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

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

Write-up: Miscarriage


VAERS ID: 1578479 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Alaska  
Vaccinated:2021-04-30
Onset:2021-05-03
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-08-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Cerebral haemorrhage, Cervical dilatation, Cervical discharge, Cervix disorder, Exposure during pregnancy, Foetal death, Postpartum disorder, Pre-eclampsia, Premature baby, Premature labour, Uterine spasm
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Hypertension (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Neonatal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: Contrast dye
Diagnostic Lab Data:
CDC Split Type:

Write-up: Uterine cramping led to preterm birth/loss. No prior history of preterm labor or incompetent cervix. Cervix was long and closed at 18-week checkup. Got vaccinated at 20 weeks. Increased discharge and cervical dilation week following vaccination with preterm delivery exactly 2 weeks post vaccination (Moderna on 30 April) on 14 May at 22 weeks gestation. Baby did not survive. Following delivery, I had a brain bleed and postpartum preeclampsia.


VAERS ID: 1389711 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-01
Onset:2021-05-03
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-06-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM4965 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Foetal death, Maternal exposure timing unspecified, 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), 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: Lactation decreased; Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test; Test Date: 20210503; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:fetus had stopped developing
CDC Split Type: GBPFIZER INC2021606814

Write-up: Maternal exposure during pregnancy; Fetal death; This is a spontaneous report from a contactable consumer received from a regulatory authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202105251429163220-VVE2T, Safety Report Unique Identifier GB-MHRA-ADR 25356737. A 40-year-old pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EM4965), via an unspecified route of administration on 01May2021 as single dose for covid-19 immunisation. Medical history included lactation decreased and pregnancy (patient no longer pregnant at the time of reporting), as reported. 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. Concomitant medication included folic acid taken for folic acid supplementation, start and stop date were not reported. The patient experienced maternal exposure during pregnancy and fetal death occurred on 03May2021. The patient underwent lab tests and procedures which included COVID-19 virus test negative on an unspecified date; an ultrasound scan on 03May2021 found that the fetus had stopped developing around a couple of days after injection. Outcome was unknown. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1289290 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-12
Onset:2021-05-04
   Days after vaccination:22
Submitted: 0000-00-00
Entered: 2021-05-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 042B1A / 1 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Reason for testing:Advanced Maternal Age Specimen Type: 1 Gestational Age (wks): Number of Fetuses: 1 Fetal Fraction Estimate: EDD: 10/19/21 Maternal Age at EDD: 36 IVF Pregnancy: No Noninvasive Prenatal Testing by Next Generation Sequencing NEGATIVE/NO ANEUPLOIDY DETECTED 0.40% CHROMOSOME TESTED Chromosome 21 Chromosome 18 Chromosome 13 Sex Chromosomes NEGATIVE: No aneuploidy detected; Consistent with two copies of chromosome 13 NEGATIVE: No aneuploidy detected; Consistent with two copies of chromosome 18 NEGATIVE: No aneuploidy detected; Consistent with two copies of chromosome 21 NEGATIVE: No aneuploidy detected; Consistent with two copies of sex chromosomes (XY) EXAM INFORMATION Plurality: 1 -------------------------------------------------------------------- FETAL MEASUREMENTS meas wks [+ / -] (Range) % CRL:5.3 cm 12w0d -------------------------------------------------------------------- COMPUTATIONS Prior Report: 3/4/2021 [Average] 15w4d EDD: 10/22/2021 Sono GA: 12w0d Method: Average -------------------------------------------------------------------- INDICATIONS FOR SONOGRAPHY Reason: Reason: 16 weeks no fetal heartbeat seen. Please confirm If after hours, there needs to be MD to MD contact for scheduling. -------------------------------------------------------------------- COMMENTS No FHB visualized. Priority Report. Preliminary prepared by Sonographer - FON on 5/4/2021 1:10:02 PM. Sonographer: Sonographer - FON Electronically signed and authenticated by: MD FON on 5/4/2021 1:59:02 PM
CDC Split Type:

Write-up: On 3/4/21, I was informed that I was pregnant with my 4th child. On 4/12/21, I was scheduled for my 1st dose of the Moderna as well as having a first trimester NCIT testing being done. At that exam, my provider was able to find a fetal heart rate (177), he was dated to be approximately 12 weeks and 6 days, and there were no concerns at that time regarding physical abnormalities or brain deformities. Additionally, I was sent out for bloodwork to rule out Trisomies and determined gender of the baby. The results of that lab work came back as negative and we were expecting our first son October 19, 2021. However, yesterday, 5/4/21, I attended my monthly prenatal appointment and the provider informed me that she could not find a heartbeat. She used a doppler scanner and then the in office ultrasound machine; neither of which detected a heartbeat. I was sent out to Radiology for a formal scan to refute or affirm the findings. Sadly, the results came back that I had lost my child. There was no heartbeat found and the results showed that my child stopped growing and remained 12 weeks in size. I am scheduled to have my pregnancy evacuated Friday, 5/7/21 at 1040a. While I am aware that miscarriage in 1 in 4 women, I cannot in good faith say that the vaccine may have contributed to my pregnancy loss. The only change in my routine was the addition of the vaccine. I am hopeful that this pain will not be felt by others and can be researched further to ensure fertility loss or future pregnancy loss isnt a norm following this vaccine. Additionally, I have had 3 full term, healthy pregnancies prior to this miscarriage. None of these pregnancies had complications and the children were birthed without issue.


VAERS ID: 1292469 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-05-03
Onset:2021-05-04
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-05-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0179 / 2 LA / SYR

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

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

Write-up: Was 5.5 weeks pregnant. Had the shot, felt strange that night, miscarried the next day.


VAERS ID: 1296125 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: New York  
Vaccinated:2021-04-19
Onset:2021-05-04
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-05-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0162 / 1 UN / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Medical marijuana dextroamphetamine-amphetamine 25mg Prenatal vitamins famotidine 20mg Sertaline 100mg
Current Illness: Nausea due to pregnancy
Preexisting Conditions: Anxiety & depression
Allergies: NKDA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Two weeks after the first vaccine was administered the patient experience fetal death intrauterine. Pt was 18 weeks and 5 days. G4P3 EDD 10/3/21


VAERS ID: 1310414 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Utah  
Vaccinated:2021-03-12
Onset:2021-05-04
   Days after vaccination:53
Submitted: 0000-00-00
Entered: 2021-05-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 031M20A / 1 AR / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 031A214 / 2 AR / IM

Administered by: Public       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal death, Induced labour, Second trimester pregnancy, Ultrasound antenatal screen abnormal
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal Multi-Vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: NKDA
Diagnostic Lab Data: Prenatal lab work 2/22/2021 WNL. Routine anatomy scan on 5/4/2021 fetal heartbeat not detected. Follow up ultrasound to confirm IUFD on 5/5/2021 Hospitalization for induction of labor on 5/6/2021. Fetus delivered at 21:02 hours. Pathology pending.
CDC Split Type:

Write-up: G6P4 Patient with estimated due date of 9/17/2021 presented for 20-week ultrasound on 5/4/2021. No heartbeat detected, diagnosis of 2nd trimester intrauterine fetal demise of fetus weighing approx. 300 grams delivered after induction of labor on 5/6/2021. Previously uncomplicated pregnancy with FHT last auscultated on 4/19/2021. 4 previous uncomplicated full-term deliveries. 1 miscarriage at ~8 weeks between first and 2nd pregnancy in ~2008


VAERS ID: 1310564 (history)  
Form: Version 2.0  
Age: 45.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-10
Onset:2021-05-04
   Days after vaccination:114
Submitted: 0000-00-00
Entered: 2021-05-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / IM

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

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

Write-up: Rare Birth defect, Opmhocele which resulted in miscarriage 2nd trimester. Dr. covering for patient''s normal Dr. stated this rare birth defect was seen twice this month.


VAERS ID: 1444839 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-26
Onset:2021-05-04
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210510; Test Name: sars-cov-2 test; Result Unstructured Data: Test Result:unknown result
CDC Split Type: FRPFIZER INC2021730010

Write-up: Pregnancy loss <20 weeks gestation; This is a spontaneous report from a contactable physician downloaded from a regulatory authority-WEB FR-AFSSAPS-RN20211484, Safety Report Unique Identifier FR-AFSSAPS-2021058288. A 34-year-old female patient received first dose of bnt162b2 (COMIRNATY), intramuscular on 26Apr2021 (Batch/Lot number was not reported) as single dose for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. At the time of vaccination, the patient was pregnant with twins (16 weeks + 5 days at 05May2021). She had a late miscarriage on 04May2021. She was taken into emergency care on 05May2021. One of the two fetuses died. Continuation of the pregnancy. The mother reported she became pregnant while taking bnt162b2. The patient underwent lab tests and procedures which included sars-cov-2 test: unknown result on 10May2021. The outcome of event was recovered with sequelae on 04May2021. No follow-up attempts are possible. No further information expected. Information on batch/lot number cannot be obtained.


VAERS ID: 1681089 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-04
Onset:2021-05-04
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-09-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: IRON; FOLIC ACID; VIT D3
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 2021; Test Name: Pregnancy test; Test Result: Positive ; Test Date: 2021; Test Name: Ultrasound fetal; Result Unstructured Data: Test Result:Lifeless fetus
CDC Split Type: NOPFIZER INC202101095424

Write-up: HEADACHE; MISSED ABORTION; she got a positive pregnancy test approximately 3 weeks after she got vaccinated, and was therefore pregnant at the time of vaccination without knowing; This is a spontaneous report from a non-contactable consumer downloaded from the regulatory authority-WEB, regulatory authority number NO-NOMAADVRE-PASRAPP-2021-U432gd. A 29-year-old female patient received bnt162b2 (COMIRNATY), dose 1 intramuscular on 04May2021 (at the age of 29-year-old) (Batch/Lot Number was not reported) as dose 1, single for covid-19 immunisation. Medical history was not reported. Concomitant medications included iron, folic acid, colecalciferol (VIT D3) and a multivitamin. On 04May2021, the patient experienced headache. In 2021, the patient experienced missed abortion. The patient reported that she got a positive pregnancy test approximately 3 weeks in 2021 after she got vaccinated and was therefore pregnant at the time of vaccination without knowing. She had an early ultrasound fetal that was conducted a couple of weeks later in 2021, and showed lifeless fetus. The events were considered as other serious, important medical events. Outcome of event headache was recovered on 06May2021; and outcome of the rest of events was recovered with sequel in 2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Reporter''s Comments: The patient reports that she got a positive pregnancy test approximately 3 weeks after she got vaccinated, and was therefore pregnant at the time of vaccination without knowing. The patient reports that an early ultrasound was conducted a couple of weeks later, and that the fetus was lifeless.


VAERS ID: 1296619 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-04-12
Onset:2021-05-05
   Days after vaccination:23
Submitted: 0000-00-00
Entered: 2021-05-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 039A21A / 1 LA / SYR

Administered by: Private       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? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin and probiotic taken daily
Current Illness: Ulcerative Colitis
Preexisting Conditions: Ulcerative Colitis
Allergies: Allergic to peanuts, adverse GI reactions to dairy and gluten
Diagnostic Lab Data: Sonogram could not find fetus. Blood test showed HCG levels had dropped from the week prior, confirming the miscarriage.
CDC Split Type:

Write-up: Miscarriage at 6.5 weeks of pregnancy. Estimated due date was 12/25. First pregnancy.


VAERS ID: 1327724 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-04-15
Onset:2021-05-05
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-05-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0162 / 2 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Exposure during pregnancy, Haemorrhage, Premature separation of placenta, Stillbirth, Thrombosis, Vasculitis
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Thrombophlebitis (broad), Vasculitis (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Immune-mediated/autoimmune disorders (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, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamins, low-dose aspirin, magnesium supplement, vitamin B2 supplement
Current Illness:
Preexisting Conditions:
Allergies: Codeine, shellfish
Diagnostic Lab Data: Placenta pathology report showed vasculitis and blood clots may have caused or contributed to the abruption.
CDC Split Type:

Write-up: Placental abruption (with heavy bleeding) occurred two days short of week 36 in first pregnancy (which was achieved via IVF with PGS-tested embryo), resulting in stillbirth on 5/6/2021; baby was 4lb 8oz upon delivery. Due date was June 4, 2021.


VAERS ID: 1374101 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Hawaii  
Vaccinated:2021-05-05
Onset:2021-05-05
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8735 / 1 LA / IM

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

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

Write-up: Systemic: Abdominal Pain-Medium, Systemic: Miscarriage-Severe, Additional Details: Pt had miscarriage after first dose of Pfizer vaccination. Bleeding started hours after shot.


VAERS ID: 1402256 (history)  
Form: Version 2.0  
Age: 45.0  
Sex: Female  
Location: Arkansas  
Vaccinated:2021-03-29
Onset:2021-05-05
   Days after vaccination:37
Submitted: 0000-00-00
Entered: 2021-06-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / IM

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

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

Write-up: Became pregnant after first covid vaccine given March 1, 2021. Received 2nd vaccine on March 29, 2021. Miscarriage occurred May 5th 2021 resulting in D&C and overnight hospitalization.


VAERS ID: 1545113 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-03-12
Onset:2021-05-05
   Days after vaccination:54
Submitted: 0000-00-00
Entered: 2021-08-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6209 / 1 - / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8733 / 2 - / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: None
Preexisting Conditions: Grave''s Disease
Allergies: NKDA
Diagnostic Lab Data: 8/3 Obstetrics US with no fetal hear tones and 8/6 D&C was preformed. For May 2021 event, please contact patient OB office.
CDC Split Type:

Write-up: Patient had two miscarriages after receiving vaccines.


VAERS ID: 1352818 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-03
Onset:2021-05-05
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-05-27
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: SYMBICORT TURBUHALER; CERTOLIZUMAB PEGOL
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Disease risk factor
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLPFIZER INC2021539527

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer downloaded from the Regulatory Authority-WEB, regulatory authority number NL-LRB-00533628. This is the maternal report. A 29-year-old female patient received bnt162b2 (COMIRNATY), dose 1 via an unspecified route of administration on 03May2021 as 0.3 ml single dose for covid-19 immunisation. Medical history included disease risk factor from an unknown date and unknown if ongoing. Concomitant medications included budesonide, formoterol fumarate (SYMBICORT TURBUHALER) taken for an unspecified indication, start and stop date were not reported; certolizumab pegol taken for an unspecified indication, start and stop date were not reported. The patient experienced miscarriage on 05May2021 with outcome of unknown. The mother was 4 Weeks pregnant at the onset of the event. No follow-up attempts are possible, information on batch number cannot be obtained.


VAERS ID: 1358959 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-19
Onset:2021-05-05
   Days after vaccination:47
Submitted: 0000-00-00
Entered: 2021-05-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER1749 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain lower, Abortion missed, Maternal exposure during pregnancy, Muscle spasms, SARS-CoV-2 test, Ultrasound scan, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Dystonia (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), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CYCLIZINE; FOLIC ACID; IBUPROFEN; MISOPROSTOL; PARACETAMOL
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid supplementation (FOLIC ACID); Headache (PARACETAMOL); Infection; Lactation decreased; Miscarriage; Pregnancy (Patient no longer pregnant at the time of reporting.); Suspected COVID-19
Allergies:
Diagnostic Lab Data: Test Date: 20210121; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:Yes - Positive COVID-19 test; Test Date: 20210510; Test Name: Ultrasound; Result Unstructured Data: Test Result:missed miscarriage
CDC Split Type: GBPFIZER INC2021549074

Write-up: Maternal exposure during pregnancy; missed miscarriage; Bleeding and cramping ongoing; Bleeding and cramping ongoing; lower stomach twinges started on 05 - may - 2021; This is a spontaneous report from a contactable consumer received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202105140907428470-Z8ZFX, Safety Report Unique Identifier GB-MHRA-ADR 25297087.A 30-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 19Mar2021 (Lot Number: ER1749) as 1ST DOSE, SINGLE for covid-19 immunisation. Medical history included Lactation decreased, infection, Miscarriage, pregnancy. Patient no longer pregnant at the time of reporting , suspected covid-19 from 22Jan2021 to 05Feb2021, vitamin supplementation, FOLIC ACID, headache, PARACETAMOL. Concomitant medication(s) included cyclizine taken for an unspecified indication, start and stop date were not reported; folic acid taken for vitamin supplementation, start and stop date were not reported; ibuprofen taken for an unspecified indication, start and stop date were not reported; misoprostol taken for an unspecified indication, start and stop date were not reported; paracetamol taken for headache, start and stop date were not reported.The patient experienced miscarriage on an unspecified date with outcome of recovering, lower stomach twinges started on 05 may 2021 on 05May2021 with outcome of recovering, maternal exposure during pregnancy on an unspecified date with outcome of unknown and Bleeding and cramping ongoing with outcome of unknown. The patient underwent lab tests and procedures which included sars-cov-2 test: yes - positive covid-19 test on 21Jan2021, ultrasound scan: missed miscarriage on 10May2021.Additional information: Very light brown spotting and very mild lower stomach twinges started on 05May2021, and increased slightly on 07-May-2021. Urgent ultrasound carried out on 10May2021 confirmed a missed miscarriage (potentially embryo stopped developing around week 7). Received medical management (misoprostol) to complete miscarriage in addition to paracetamol, Ibuprofen and Cyclizine to manage miscarriage symptoms.Patient has not tested positive for COVID-19 since having the vaccine.Details of previous pregnancies: No previous pregnancies. Pfizer vaccine was administered on 19Mar2021 (at week 3 of pregnancy, before positive pregnancy test), on guidance from GP.Patient was exposed to the medicine first-trimester (1-12 weeks).Details of scans or investigations: Emergency scan at 10 weeks + 3 days (10-May-2021), showed a missed miscarriage, embryo was 9.6mm; all other maternal physiology normal.Had COVID-19 infection at the end of January 2021, confirmed by positive PCR test on 21Jan2021. Patient is not enrolled in clinical trial Patient is not currently breastfeeding. Events were reported as medically significant. No follow-up attempts are needed. No further information is expected.


VAERS ID: 1480298 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-24
Onset:2021-05-05
   Days after vaccination:42
Submitted: 0000-00-00
Entered: 2021-07-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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: Abstains from alcohol; Delivery (The patient have given birth to 2 children before this incident.); Non-smoker
Allergies:
Diagnostic Lab Data:
CDC Split Type: NOPFIZER INC2021781468

Write-up: Exposure BEFORE pregnancy; SPONTANEOUS ABORTION; This is a spontaneous report from a non-contactable consumer or other non hcp downloaded from the Regulatory Authority, regulatory authority number NO-NOMAADVRE-PASRAPP-2021-Ueej15. This case was received from patient/consumer with the world-wide case reference no. NO-NOMAADVRE-PASRAPP-2021-Ueej15. A 33-years-old female patient received first dose of bnt162b2 of (COMIRNATY, Solution for injection, Batch/Lot number was not reported), via an intramuscular route of administration, administered in left arm on 24Mar2021 10:33 as single dose for COVID-19 immunization. The patient medical history included abstains from alcohol, delivery (The patient had given birth to 2 children before this incident) and non-smoker for all from an unknown date and unknown if ongoing. The patient was not pregnant at time of vaccination. The patient''s concomitant medications were not reported. The patient reports not taking any medicines or dietary supplement, and not having any diseases. It was reported that the patient reported having two kids and was waiting for the third. The patient got pregnant approximately 1 week after getting the vaccine, the embryo died in week 5. The patient reported not experiencing spontaneous abortion before. The patient reported no knowing if this has a connection with the vaccine or not, but the patient wanted to inform about this since it was her first spontaneous abortion and it happened during the same period the vaccine was taken. On 05May2021 the patient experienced spontaneous abortion and exposure before pregnancy on an unspecified date. The outcome of event spontaneous abortion was recovered on an unspecified date, while the event of exposure before pregnancy outcome was unknown. Reporter''s comment: The patient reports not taking any medicines or dietary supplement, and not having any diseases. The patient reports having two kids, and was waiting for the third. The patient reports getting pregnant approximately 1 week after getting the vaccine, the embryo died in week 5. The patient reports not experiencing SPONTANEOUS ABORTION before. The patient reports no knowing if this has a connection with the vaccine or not, but the patient wanted to inform about this since it was her first SPONTANEOUS ABORTION and it happened during the same period the vaccine was taken. No more information available regarding this case. No follow-up attempts possible. No further information expected. Lot/Batch number cannot be obtained.


VAERS ID: 1786896 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-05-05
Submitted: 0000-00-00
Entered: 2021-10-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Disease risk factor
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLJNJFOC20211013527

Write-up: MATERNAL EXPOSURE DURING PREGNANCY; Miscarriage; This spontaneous pregnancy report received from a consumer via a Regulatory Authority (EVHUMAN Vaccines, NL-LRB-00693738) on 07-OCT-2021 and concerned a 33 year old female. The patient''s weight was 70 kilograms, and height was 173 centimeters. The patient''s past medical history included: disease risk factor. The patient was gravida 1, para 0. The gestation period was 2 weeks with retrospective pregnancy and outcome spontaneous abortion. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 21C10-02 expiry: UNKNOWN) 0.5 ml, 1 dosage forms, 1 total, administered on 12-APR-2021 for covid-19 immunisation. No concomitant medications were reported. On 05-MAY-2021, the patient experienced miscarriage (miscarriage on 05-May (5.5 weeks pregnant)). On an unspecified date, the patient experienced maternal exposure during pregnancy. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the maternal exposure during pregnancy and miscarriage was not reported. This report was serious (Other Medically Important Condition).


VAERS ID: 1822349 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-05-05
Submitted: 0000-00-00
Entered: 2021-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Influenza, Menstrual disorder
SMQs:, Termination of pregnancy and risk of abortion (narrow), Infective pneumonia (broad), Opportunistic infections (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: Crohn''s
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnant
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEJNJFOC20211051117

Write-up: FLU SYMPTOMS; MENOXENIA; MISCARRIAGE OF PREGNANCY; This spontaneous report received from a consumer via a Regulatory Authority (DE-PEI-CADR2021190126) on 25-OCT-2021 and concerned a 32 year old female of unspecified race and ethnicity. The patient''s weight was 75 kilograms, and height was 156 centimeters. The patient''s past medical history included: pregnant, and concurrent conditions included: crohn''s. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: XD955 expiry: UNKNOWN) dose was not reported, 1 total administered on 05-MAY-2021 for prophylactic vaccination. No concomitant medications were reported. On 05-MAY-2021, the patient experienced flu symptoms, menoxenia and miscarriage of pregnancy. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from flu symptoms, menoxenia, and miscarriage of pregnancy on 11-OCT-2021. This report was serious (Other Medically Important Condition).


VAERS ID: 1300482 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-03
Onset:2021-05-06
   Days after vaccination:33
Submitted: 0000-00-00
Entered: 2021-05-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 024C21A / 2 LA / SYR

Administered by: School       Purchased by: ?
Symptoms: Abortion spontaneous, Haemorrhage, Muscle spasms
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Dystonia (broad), Termination of pregnancy and risk of abortion (narrow)

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

Write-up: Miscarriage Got my first Moderna shot on 04/03/2021, second Moderna shot on 05/05/2021. Cramping on April 26, 2021 as I was 5 weeks pregnant, bleeding on 05/06/2021 confirming miscarriage. Last period was 03/25/2021, due date was planned 12/30/2021.


VAERS ID: 1302256 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2021-04-16
Onset:2021-05-06
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-05-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Wellbutrin
Current Illness: No
Preexisting Conditions: No
Allergies: Penicillin
Diagnostic Lab Data: No tests taken on me. We sent the fetus out for further testing but haven?t gotten results yet.
CDC Split Type:

Write-up: I had a miscarriage at my 18 week check-up. They estimated the baby died around 16 weeks and 5 days. I had gotten my 1st covid vaccine shot at 15 weeks pregnant. My baby had been healthy with no genetic disorders detected at the time of the miscarriage. I don?t know if this could be related to the vaccine, but wanted to report.


VAERS ID: 1309753 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-17
Onset:2021-05-06
   Days after vaccination:19
Submitted: 0000-00-00
Entered: 2021-05-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Disseminated intravascular coagulation, Exposure during pregnancy
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), 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), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: None
Current Illness: COVID 3/28/21
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pregnant EDD: 12/19/2021 Dx: DIC complications after miscarriage


VAERS ID: 1341438 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-04-01
Onset:2021-05-06
   Days after vaccination:35
Submitted: 0000-00-00
Entered: 2021-05-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Haemorrhage in pregnancy, Ultrasound abdomen abnormal, Uterine dilation and evacuation
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: No
Preexisting Conditions: No
Allergies: Sulfa drugs
Diagnostic Lab Data: Ultrasounds on 4/22/21 5/7/21. D&E 5/20/21. Waiting for genetic testing.
CDC Split Type:

Write-up: Received first dose on 4/17/21. Period late and not recorded on v-safe. Estimated due date was 12/21/21. Had 6 week ultra sound and bleeding shown on ultra sound. At 7 weeks light bleeding. At 8 week ultrasound no fetal pole visible. Wanted to report incident. Expecting genetic testing of embryo.


VAERS ID: 1349559 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2021-04-16
Onset:2021-05-06
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-05-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0161 / 1 LA / -

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

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: WELLBUTRIN
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: COVID-19; Penicillin allergy
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021523737

Write-up: I had a miscarriage and they estimated the baby died at 16 weeks 5 days.; This is a spontaneous report from a contactable consumer (patient). A 36-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in arm left on 16Apr2021 14:00 (Batch/Lot Number: EW0161) as single dose for COVID-19 immunization. Medical history included allergies penicillin and COVID-19. The patient''s concomitant medications included bupropion hydrochloride (WELLBUTRIN) within 2 weeks of vaccination. Last menstrual period (LMP) was reported as 30Dec2020. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No other medications the patient received within 2 weeks of vaccination. Prior to vaccination, patient was diagnosed with COVID-19. Since the vaccination, patient has not been tested for COVID-19. On 06May2021 16:00, the patient had a miscarriage and they estimated the baby died at 16 weeks 5 days. There were no genetic disorders detected, so the cause was unknown. Patient thought maybe the vaccine could have something to do with it. The adverse event result in Doctor or other healthcare professional office/clinic visit. Treatment received for the adverse event included fetal demise removal. Outcome of the event was recovering. Information on Lot/Batch number was available. Additional information has been requested.


VAERS ID: 1361336 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2021-04-26
Onset:2021-05-06
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-05-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 AR / SYR

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Blood test abnormal, Exposure during pregnancy, Human chorionic gonadotropin abnormal, Progesterone decreased, 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), Fertility disorders (narrow), Sexual dysfunction (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: adderall
Current Illness:
Preexisting Conditions:
Allergies: NKA
Diagnostic Lab Data: 5/6/21: OBGYN appt ultrasound and bloodwork - dilated yolk sac and hcg and progesterone levels too low 5/11/21: Bloodwork 5/12/21: ultrasound with specialist at hospital 5/15/21: miscarried 5/17/21: Bloodwork
CDC Split Type:

Write-up: Birthed 3 healthy children without complications (other than c section at full term) within the past 5 years. I found out I was pregnant the night I received my second dose of the covid-19 Pfizer vaccine. A little over a week later at my OBGYN appointment, I was told that there was something wrong. I was only 5 weeks pregnant. At 6 weeks and 3 days, I had a miscarriage (naturally).


VAERS ID: 1457404 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-04-12
Onset:2021-05-06
   Days after vaccination:24
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM9809 / UNK RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Autopsy, Exposure during pregnancy, Foetal placental thrombosis, Investigation, Laboratory test, Nodule, Stillbirth, Thrombosis, Ultrasound scan
SMQs:, Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Thrombophlebitis (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Daily pre-natal vitamin (Nature Made brand, prenatal with DHA)
Current Illness: None.
Preexisting Conditions: None.
Allergies: None.
Diagnostic Lab Data: Placenta analysis and fetal autopsy - May 7 Various blood tests to test for coagulation - May 7 and 10 Genetic carrier screening - June 2 Series of blood tests, purposes unknown to me (too technical, but I have them) - June 2
CDC Split Type:

Write-up: Note that these events occurred in another country where I am currently working. Dr. can respond to questions about this vaccination. Dr is the specialist who saw me....... after the adverse event to assess possible phsyiological conditions that could have caused the stillbirth and preconception counseling for the future--I only listed her as your form does not allow international numbers, but she can speak to the labs and autopsy and generally on behalf of my obstetrical/gynecological health. I experienced a late-term stillbirth approximately 24 days after the second dose of the pfizer COVID-19 vaccine. I had otherwise not experienced any side effects with either dose of the vaccine. I received my vaccine via the clinic. The stillbirth likely occurred on May 6, but was not confirmed by ultrasound until the morning of May 7. The only sign of the IUFD was cessation of the baby''s movements; the event was not accompanied by any pain or bleeding. There was no physical trauma (fall, force to the abdomen, etc). The only event of note between the second dose and the stillbirth was that I went on a four-hour hike Placenta analysis and the fetal autopsy confirmed thrombosis in the placenta''s chorionic vessels and a focal increase in syncytial knots, with a diagnosis that placental changes were consistent with fetal vascular malperfusion. The fetus was anatomically normal and appropriate size and weight for gestational age (28 weeks and 6 days per ultrasound). The fetus had no abnormalities or other signs of trauma or infection beyond expected maceration. My ob/gyn and Dr. both opine that the blood clots caused IUFD, with the event being very sudden/acute. There was no explanation identified for what could have caused the sudden blood clots. This was my first pregnancy. I was 29 weeks 0 days along when the IUFD was confirmed, with an estimated due date of July 20, 2021. The pregnancy was unremarkable up until the IUFD. Birth weight was approximately 1230 grams.


VAERS ID: 1722731 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-05-05
Onset:2021-05-06
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-09-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0167 / 2 RA / SYR

Administered by: Military       Purchased by: ?
Symptoms: Anticoagulant therapy, Blood test, Cardiac disorder, Chills, Computerised tomogram thorax abnormal, Dyspnoea, Exposure during pregnancy, Feeling abnormal, Heart rate increased, Influenza, Muscle strain, Nervousness, Premature delivery, Pulmonary thrombosis, Pyrexia, Thrombosis, Ultrasound scan, X-ray
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Embolic and thrombotic events, venous (narrow), Thrombophlebitis (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Dehydration (broad), Opportunistic infections (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 4 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Flintstone vitamins, Flonase, Flovent, Albuterol, 81mg aspirin, and magnesium
Current Illness: asthma and gestational diabeties
Preexisting Conditions:
Allergies: contrast dyes and latex
Diagnostic Lab Data: Hospital: 6 May 2021 Xrays, ultrasounds, blood test, and CT scan Different Hospital: continued to monitor and perform test 6-9 May. No additional scans ran due to pregnancy.
CDC Split Type:

Write-up: Pregnant at the time Estimated Date of Delivery: 17 July 2021 Delivery 34/35 weeks 5 May 2021 had a strange feeling, but ignored because everyone I know complained about the 2d dose causing flu symptoms 6 May 2021: started getting worse with rapid heart rate, hard time breathing, chills and fever (105). Went to Hospital because I was nervous about the temperature while being pregnant. A serious a test were ran and I was initially told I was fine; however, my temperature slightly went down and my heart and breathing continued to get worse. A CT scan showed multiple clots on the lungs and a strain on my heart. Was transported by an ambulance to different Hospital and stayed for about 4 days. Was placed on Lovenox.


VAERS ID: 1301681 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-12
Onset:2021-05-06
   Days after vaccination:24
Submitted: 0000-00-00
Entered: 2021-05-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM9809 / 2 LA / IM

Administered by: Other       Purchased by: ?
Symptoms: Adverse event, Pregnancy, Stillbirth, 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? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Pre-natal vitamin; no self-prescribed medications, OTC medications, supplements or herbal products.
Current Illness: No illness
Preexisting Conditions: In good general health
Allergies: No known allergies to medications, foods or other products.
Diagnostic Lab Data: Obstetrical ultrasound on May 7, 2021 revealed no fetal activity, no cardiac contractions, no other activity.
CDC Split Type:

Write-up: Estimated date of delivery: July 20, 2021; Adverse event: Intrauterine fetal demise at 29 weeks estimated gestation; This is the first pregnancy; In good general health before and during pregnancy.


VAERS ID: 1392289 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-06
Onset:2021-05-06
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? 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: BRPFIZER INC2021627894

Write-up: fetal death; pregnant woman was applied the first dose of Pfizer vaccine against covid19; This is a spontaneous report from a contactable physician. A female patient of an unspecified age received bnt162b2 (COMIRNATY), dose 1 via an unspecified route of administration on 06May2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The pregnant woman physician accompany with prenatal care applied the first dose of Pfizer vaccine against covid19 on 06May2021. The pregnancy was of low risk and without any complications until then. However, on 27May2021, fetal death was identified at around 19 weeks of gestational age. Fetal death is yet to be investigated. Information on the lot/batch number has been requested.; Sender''s Comments: As there is temporal association in the case provided, the causal association between the events foetal death, exposure during pregnancy and the suspect BNT162B2 cannot be excluded. However, limited medical information precludes further assessment. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1312628 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Georgia  
Vaccinated:2021-04-01
Onset:2021-05-07
   Days after vaccination:36
Submitted: 0000-00-00
Entered: 2021-05-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 003C21A / 1 RA / IM

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

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

Write-up: Miscarriage


VAERS ID: 1339093 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: California  
Vaccinated:2021-05-07
Onset:2021-05-07
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Muscle spasms, Pregnancy, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Dystonia (broad), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

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

Write-up: I was 7 weeks pregnant and received 2nd Pfizer vaccine, on the same day started having virginal bleeding and crumping, had miscarriage next day.


VAERS ID: 1446568 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Vermont  
Vaccinated:2021-04-23
Onset:2021-05-07
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-07-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 001C21A / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Placental disorder, Spontaneous 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: Unsure; patient does not fill prescriptions here. Did not receive this information prior to the patient leaving.
Current Illness: None.
Preexisting Conditions: Multiple Sclerosis
Allergies: No known allergies.
Diagnostic Lab Data: Unsure.
CDC Split Type:

Write-up: Patient reported that she miscarried ~2 weeks following her vaccine (dose #1 of Moderna). She waited for a prolonged period of time prior to receiving 2nd dose (which is when she reported this to us). Some of the exact details of timing were difficult for her to remember. However, she stated that she was in her 1st trimester and she had miscarried due to placental problems - spontaneous bleeding, leading to miscarriage.


VAERS ID: 1454285 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-03-24
Onset:2021-05-07
   Days after vaccination:44
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 020B21A / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Foetal heart rate abnormal, Human chorionic gonadotropin positive, Infection, Pyrexia, Sepsis, Ultrasound antenatal screen abnormal, Uterine dilation and curettage
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Tumour markers (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), Normal pregnancy conditions and outcomes (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Sepsis (narrow), Opportunistic infections (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? Yes, 4 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Loratadine, Pre-Natal vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: Sulfa, Benadryl, Erythromycin, Doxycycline, Penicillin, Clindamycin
Diagnostic Lab Data: OB ultrasound - May 7 - unable to find heartbeat HCG Quant - May 7 - 33,385.5mIU/mL HCG Quant - May 10 - 25,163.2mIU/mL OB ultrasound - May 11 - no cardiac activity Emergent D&C due to signs on sepsis - May 21 There''s more but I''ve just gotten the 5 minute notice......
CDC Split Type:

Write-up: I had my second dose of the Covid19 vaccine on March 24, 2021. I didn''t know at the time that I was pregnant, it was very early. Received a positive confirmation on April 14, 2021. At this time I was about 6 weeks along. Due date was estimated for the beginning to mid- December. On May 7th I had my first appointment with an OB, at that time she was unable to find a heartbeat. HCG quants were checked and I was sent for a more extensive ultrasound on May 11. Miscarriage was confirmed that day. Scheduled a D&C for May 24th, on the 21st I spiked a fever and was exhibiting signs on sepsis. That evening an emergent D&C was performed. Seemed to be on the mend the next morning and was sent home with oral antibiotics. On the 25th I spiked another fever and was advised by my physician to get to the emergency room. Spent the next three nights in the hospital with IV antibiotics. Came home with a couple different oral antibiotics (Flagyl and Clindamycin) for the next 2 weeks. This seemed to cover the infection.


VAERS ID: 1647111 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-04-24
Onset:2021-05-07
   Days after vaccination:13
Submitted: 0000-00-00
Entered: 2021-08-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8736 / 2 RA / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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: None
Allergies:
Diagnostic Lab Data: Test Name: HCG testing 3 times; Result Unstructured Data: Test Result:Unknown results
CDC Split Type: USPFIZER INC202101041640

Write-up: miscarriage; This is a spontaneous report from a contactable consumer (patient). A 30-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 2 via an unspecified route of administration, administered in Arm Right on 24Apr2021 11:00 (Batch/Lot Number: ER8736) age at vaccination of 30-years-old, as single dose, for covid-19 immunisation. Medical history was none. It was unknown if patient was pregnant and if she was pregnant at the time of vaccination. There were no concomitant medications. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in Left arm on 29Mar2021 02:45 PM (Batch/Lot Number: ER8734) age at vaccination of 30-years-old, as single dose, for covid-19 immunisation. The patient had a miscarriage on 07May2021, she found out that was pregnant on 27Apr2021. The patient believe that 2nd vaccine had something to do with miscarriage. The event was reported as serious (medically significant). Doctor visits were done and HCG testing 3 times (Unknown results). Facility where the most recent COVID-19 vaccine was administered: Pharmacy or Drug Store. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient recovered from miscarriage on an unspecified date.


VAERS ID: 1350196 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-05-07
Submitted: 0000-00-00
Entered: 2021-05-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

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: AUPFIZER INC2021537585

Write-up: Abortion spontaneous; This is a spontaneous report from a contactable other health professional. This is a report received from the regulatory authority. The regulatory authority report number is 549660. A female patient of an unspecified age received BNT162B2 (COMIRNATY Solution for injection, lot number was not reported), via an unspecified route of administration, on an unspecified date, as unknown, single, for COVID-19 immunisation. The patient was pregnant. The patient''s medical history and concomitant medications were not reported. The patient experienced abortion spontaneous on 07May2021. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1389707 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-15
Onset:2021-05-07
   Days after vaccination:22
Submitted: 0000-00-00
Entered: 2021-06-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM4965 / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage; Missed abortion (first pregnancy); Pregnancy (Patient no longer pregnant at the time of reporting.); Suspected COVID-19 (Unsure when symptoms stopped)
Allergies:
Diagnostic Lab Data: Test Date: 20210507; Test Name: ultrasound scan; Result Unstructured Data: Test Result:foetal growth stopped at week 9
CDC Split Type: GBPFIZER INC2021606833

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer (patient) received from the Agency Regulatory Authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202105251417135960-IAO7R, Safety Report Unique Identifier GB-MHRA-ADR 25356692. A 32-year-old female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EM4965), via an unspecified route of administration on 15Apr2021 as 2ND DOSE, SINGLE DOSE for covid-19 immunisation. Medical history included miscarriage, pregnancy, patient no longer pregnant at the time of reporting, suspected covid-19 from 01Apr2020, unsure when symptoms stopped, missed miscarriage at 12 weeks, first pregnancy. The patient had not had a COVID-19 test, was not enrolled in clinical trial and was not currently breastfeeding. Concomitant medication included folic acid taken for vitamin supplementation at 5 mg, start and stop date were not reported. The patient experienced miscarriage on 07May2021. The patient''s hospitalization was prolonged as a result of miscarriage. The mother reported she was pregnant when taking BNT162b2, 2nd dose was given at week 9, the patient was exposed to the medicine first-trimester (1-12 weeks). The mother was 12 weeks pregnant at the onset of the event. It was reported that at time of 2nd vaccine administered the patient was 9 weeks pregnant. At 12 weeks she experienced a missed miscarriage. According to the ultrasound scan completed at time of miscarriage foetal size was estimated at roughly 9 weeks suggesting pregnancy actually ended at 9 weeks despite miscarriage not occurring until 12 weeks. Understandably this could have been a natural occurrence not relating to vaccine, and just coincidence that this had happened at time of vaccine. The patient underwent lab tests and procedures which included ultrasound scan: foetal growth stopped at week 9 on 07May2021. Patient had not tested positive for COVID-19 since having the vaccine. The patient had recovered from the event on 09May2021. The reporter was unsure if the medicine had an adverse effect on any aspect of the pregnancy. No follow-up attempts are possible. No further information is expected


VAERS ID: 1417424 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-05-07
Submitted: 0000-00-00
Entered: 2021-06-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Petechiae, Pyrexia
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? 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: AUPFIZER INC2021678084

Write-up: Abortion spontaneous; Petechiae; Pyrexia; This is a spontaneous report from a contactable healthcare professional via the regulatory authority. The regulatory authority report number is 560667. A pregnant 39-year-old female patient received BNT162B2 (COMIRNATY; Lot Number was not reported), via an unspecified route of administration, on an unspecified date, as dose number unknown, single, for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. On 07May2021, the patient experienced abortion spontaneous, petechiae, and pyrexia. The patient recovered from the events in 2021. No follow-up attempts are possible; information about lot or batch number cannot be obtained.


VAERS ID: 1476507 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-07
Onset:2021-05-07
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM4965 / UNK RA / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
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: GBPFIZER INC2021827615

Write-up: had a miscarriage at 8weeks; she became pregnant while taking BNT162B2; This is a spontaneous report from a contactable consumer (patient). This consumer reported information for herself and her fetus/baby. This is a maternal report. A 34-year-old pregnant female patient received BNT162B2 (BNT162B2, PFIZER-BIONTECH, COVID-19 Vaccine Formulation: Solution for injection, Lot Number: Em4965 and Expiration date: unknown), via an unknown route of administration, administered in right arm on 07May2021 (at the age of 34-years-old) as dose number unknown, single for covid-19 immunisation. The patient medical history was not reported. There were no concomitant medications. Gestation period was 8 weeks. Due date of pregnancy was 06Jan2022. On 02Jun2021, the patient experienced reported that her baby stopped growing at 05 weeks and had a miscarriage at 08 weeks. The event resulted in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Patient received meds to expedite miscarriage as a treatment. 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. Outcome of event Abortion was reported as recovered with sequelae and other event was unknown; Sender''s Comments: Linked Report(s) : GB-PFIZER INC-2021828401 Baby Case


VAERS ID: 1499051 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-07
Onset:2021-05-07
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH J07BX03 / 1 - / OT

Administered by: Other       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? 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: FRPFIZER INC2021865054

Write-up: Miscarriage; dose 1 on 07May2021; dose 2 on 18Jun2021; This is a spontaneous report from a contactable consumer downloaded from the WEB, regulatory authority number FR-AFSSAPS-2021087784. A 30-year-old female patient received bnt162b2 (COMIRNATY), dose 1 intramuscular (left arm) on 07May2021 (Batch/Lot Number: J07BX03) as dose 1 single; and dose 2 intramuscular, administered in Arm Left on 18Jun2021 (Batch/Lot Number: J07BX03) as dose 2, single for Covid-19 immunization. The patient''s medical history was not reported. There were no concomitant medications. It was reported that on an unspecified date, the patient had spontaneous miscarriage after first injection. It was reported that the patient received a second injection of Comirnaty on 18Jun2021; on 03Jul2021 she had a spontaneous miscarriage at 5 weeks of amenorrhea, that is her third week of pregnancy. Date of onset of pregnancy: 13Jun2021. She was admitted to hospital after medical consultation and was also brought to Emergency room. It should be noted that this patient also reported a miscarriage after the first injection when she was at 5 weeks amenorrhea + 1. She therefore reported 2 consecutive miscarriages, each after vaccination against COVID-19. The outcome of event spontaneous miscarriage was recovered on 03Jul2021. No follow-up attempts are possible, no further information is expected.


VAERS ID: 1589290 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-07
Onset:2021-05-07
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-08-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ET8885 / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Lactation decreased; Pregnancy (One previous pregnancy in 2017 (successful).)
Allergies:
Diagnostic Lab Data: Test Date: 20201130; Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test; Test Name: Scan; Result Unstructured Data: Test Result:the baby had died; Comments: showed baby was 5 weeks 6 days with no heartbeat.
CDC Split Type: GBPFIZER INC202100998609

Write-up: Early miscarriage/miscarriage; Maternal exposure during pregnancy/Patient was exposed to the medicine first-trimester (1-12 weeks); This is a spontaneous report from a contactable consumer (patient). This is a report received from the Regulatory Agency (RA). Regulatory authority report number [GB-MHRA-WEBCOVID-202108032217336880-8ZPBK], Safety Report Unique Identifier [GB-MHRA-ADR 25750388]. A 33-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 07May2021 (Lot Number: ET8885), at the age of 33-years-old, as dose 1, single for COVID-19 immunisation. Medical history included lactation decreased from an unknown date and unknown if ongoing and one previous pregnancy in 2017 (successful). Concomitant medications included folic acid taken for Folic acid supplementation, start and stop date were not reported. The patient experienced maternal exposure during pregnancy on 07May2021; and Early miscarriage/miscarriage on 10May2021. The patient underwent lab tests and procedures which included COVID-19 virus test: No - Negative COVID-19 test on 30Nov2020 and scan: the baby had died (showed baby was 5 weeks 6 days with no heartbeat) on an unknown date. Patient no longer pregnant at the time of reporting. The outcome of the event ''early miscarriage/miscarriage'' was recovered on 16Jun2021 and outcome of the event ''maternal exposure during pregnancy'' was unknown. The clinical course was reported as follows: Patient does not necessarily think the miscarriage was caused by the vaccine. Due to the timings of when she had the vaccine and when the scan showed the baby had died, she thought she should report it here so that more data and information can be gathered to help. Patient has not tested positive for COVID-19 since having the vaccine. Patient was not enrolled in clinical trial. Unsure if the medicine has an adverse effect on any aspect of the pregnancy. Patient was exposed to the medicine first-trimester (1-12 weeks). Details of scans or investigations: Vaccine at 5 weeks 3 days, 9 week scan showed baby was 5 weeks 6 days with no heartbeat. Additional information: No other medicines were taken and no illnesses. Patient has not had symptoms associated with COVID-19. Patient was not currently breastfeeding. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1321950 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-04-14
Onset:2021-05-08
   Days after vaccination:24
Submitted: 0000-00-00
Entered: 2021-05-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 042B21A / 1 LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: I went to the doctor on May 12th 2021 and a miscarriage was confirmed via ultrasound and blooodowrk results. I miscarried at 6 weeks.
CDC Split Type:

Write-up: At the time of vaccination I did not know I was pregnant. I?m not sure if the vaccine had anything to do with what happened, but I would still like to report that on May 8th 2021 I started to miscarry. Any number of reasons could have caused this, the doctors do not know why, but it?s important to know I did get the first dose during the beginning of my pregnancy.


VAERS ID: 1322390 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-04-27
Onset:2021-05-08
   Days after vaccination:11
Submitted: 0000-00-00
Entered: 2021-05-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0170 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Exposure during pregnancy, Ultrasound abdomen, 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? 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: Codiene and hydrocodone
Diagnostic Lab Data: Blood panel run May 10 and May 12. Follow up panel May 17. Abdominal ultrasound May 10.
CDC Split Type:

Write-up: First does of vaccine received April 27, 2021. Positive pregnancy test April 30, 2021. First sign of miscarriage May 8, 2021. Confirmation of pregnancy via bloodwork May 10, 2021. Abdominal sonogram May 10 shows uteri lining/pregnancy stopped forming/advancing at 4-4.5 weeks gestation which falls between the dates of April 2--May 3. 11 days after receiving first dose of vaccination.


VAERS ID: 1340388 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-15
Onset:2021-05-08
   Days after vaccination:23
Submitted: 0000-00-00
Entered: 2021-05-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW1058 / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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: USPFIZER INC2021515752

Write-up: miscarriage; This is a spontaneous report from a contactable consumer (patient). A 41-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on 15Apr2021 16:00 (Batch/Lot Number: EW1058) as 2nd dose, single or covid-19 immunisation. The first dose was received on 15Mar2021 17:00 (lot number: ENLe208). The patient''s medical history was not reported. Concomitant medications were none. No other vaccine was administered in 4 weeks. Six days after receiving the 2nd shot of the Covid vaccine from Pfizer, patient conceived on 21Apr2021. After 4 weeks and 4 days of pregnancy, patient had a miscarriage on 08May2021 14:30. While a miscarriage can happen at the early stages of pregnancy, this stage was exactly when the placenta was forming and patient was wondering that the rumors about the COVID vaccine rejecting the protein of the placenta were correct. No treatment was given. Outcome of the event was not recovered. Patient did not have covid prior to vaccination and had not been tested post-vaccination.


VAERS ID: 1347465 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-05-07
Onset:2021-05-08
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-05-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0164 / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Fatigue, Foetal growth restriction, Foetal heart rate abnormal, Ultrasound foetal abnormal, Uterine dilation and curettage, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal multivitamins.
Current Illness: No.
Preexisting Conditions: ITP- blood platelet disorder.
Allergies: No.
Diagnostic Lab Data: D&C 05/19/2021 Ultrasound
CDC Split Type: vsafe

Write-up: Normal pregnancy before vaccination. After first dose I experienced vaginal bleeding and fatigue. After I fatigue, really tired that I never felt before. Felt really tired for two weeks. I miscarried my pregnancy. Baby had no heart beat and not progressing.


VAERS ID: 1426913 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-05-05
Onset:2021-05-08
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-06-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0171 / 1 LA / -

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: Medical History/Concurrent Conditions: Allergy
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021680699

Write-up: 5 days after receiving the Pfizer vaccination I ended up in the ER due to me having a miscarriage that had started approximately 4 days after the vaccination was given.; This is a spontaneous report received from a contactable consumer (patient). A 36-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 05May2021 13:00 (Batch/Lot Number: EW0171) (at age of 36 years) as DOSE 1, SINGLE for COVID-19 immunisation. Patient was pregnant at time of vaccination. Last menstrual date was on 09Apr2021. Medical history included known allergies (unspecified) and other unspecified medical history. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. There were other unspecified medications the patient received within 2 weeks of vaccination. 5 days after receiving the Pfizer vaccination, patient ended up in the ER due to having a miscarriage that had started approximately 4 days after the vaccination was given, on 08May2021 08:00 (as reported). The mother was 4 weeks pregnant at the onset of the event (also reported as 5 with unspecified unit). The mother was due to deliver on 14Jan2022. The mother delivered the pregnancy (as reported, pending clarification). The pregnancy resulted in spontaneous abortion. Adverse event resulted in Emergency room/department or urgent care. Treatment for event was unknown. The outcome of event was recovered on May2021.


VAERS ID: 1487353 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-04-17
Onset:2021-05-08
   Days after vaccination:21
Submitted: 0000-00-00
Entered: 2021-07-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0161 / 2 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Bell's palsy, Computerised tomogram head, Exposure during pregnancy, Migraine
SMQs:, Hearing impairment (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: Melatonin; Zyrtec.
Current Illness: n/a
Preexisting Conditions: Asthma; Sleep apnea; Anemia.
Allergies: Penicillin; Phenergan; Zofran; Dramamine; Lanichol.
Diagnostic Lab Data: CT scan, 7/13/2021, normal.
CDC Split Type: vsafe

Write-up: It started with headaches, they got worse and then I woke up one day with Bell''s palsy, that was on July 7, 2021. I already had an appointment set up for the 8th of July so my doctor checked me out then. My doctor gave me prednisone for five days and told me if anything got worse, to go to the ER. I ended up in the ER on 7/13/2021 because of the migraines and they did a CT scan and everything came back normal so they told me to follow up with my PCP so I am seeing her on July 22, 2021. I also had a miscarriage, I was to deliver on September 24, 2021. I was 17 weeks pregnant when I received my second dose of the vaccine. I have miscarried before as well.


VAERS ID: 1340022 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-06
Onset:2021-05-08
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-05-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain, Abortion, Foetal heart rate, Investigation, Ultrasound antenatal screen, Vaginal haemorrhage
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: fetal heart rate; Result Unstructured Data: Test Result:decreased; Test Name: HCG hormone; Result Unstructured Data: Test Result:decreased level; Test Name: investigation; Result Unstructured Data: Test Result:negative; Test Name: ultrasound; Result Unstructured Data: Test Result:positive; Comments: these indicated baby was died
CDC Split Type: SAPFIZER INC2021521203

Write-up: abortion; bleeding; abdominal pain; This is a spontaneous report from a contactable physician via information team. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on 06May2021 (Batch/Lot number was not reported) as UNKNOWN, SINGLE for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. The patient stated, "I took vaccine of COVID-19 of Pfizer on 06May2021, then I stared to have bleeding and abdominal pain since yesterday 08May2021 up to now and in ultrasound for baby, the fetal heart rate and HCG hormones show decrease level all these indicated my baby was dei (as reported) and I had an abortion. I am healthy and I did all investigation for viruses that may cause abortion 4 w ago and all negative. And I took folic acid since beginning of pregnancy. All this induced my abortion is due to COVID vaccine of Pfizer and this vaccine is not safe for pregnancy especially in first 3 months." The mother was 7 Weeks pregnant at the onset of the event. The mother was pregnant with 1 baby. The pregnancy resulted in spontaneous abortion. The outcome of events was unknown.; Sender''s Comments: Based on the information available and a close temporal association, a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported events of abortion,vaginal heamarrhage,abdominal pain. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate


VAERS ID: 1403151 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-08
Onset:2021-05-08
   Days after vaccination:30
Submitted: 0000-00-00
Entered: 2021-06-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Haemorrhage, Investigation, Pain, Ultrasound scan, Uterine contractions abnormal
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:
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Allergies:
Diagnostic Lab Data: Test Name: examination; Result Unstructured Data: Test Result:Unknown result; Test Name: diagnostic ultrasound; Result Unstructured Data: Test Result:Unknown result
CDC Split Type: CAPFIZER INC2021635675

Write-up: Miscarriage/loss of pregnancy; significant haemorrhage; pain; contractions; This is a spontaneous report from a contactable consumer (patient). A 37-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, on 08Apr2021 (Batch/Lot number was not reported), as unknown, single dose, at age 37 years old, for COVID-19 immunisation. The patient was pregnant at the time of vaccination. There was no medical history. The patient was not diagnosed with COVID-19 prior to vaccination and has not been tested for COVID-19 since the vaccination. The patient''s concomitant medications were not reported. It was reported that the due date was on 08Nov2021 and gestation period was 10 weeks. On 08May2021, the patient experienced miscarriage/loss of pregnancy with significant haemorrhage, pain, and contractions. The events resulted to emergency room/department or urgent care visit. Treatment was reported as "examination and diagnostic ultrasound". The patient underwent examination and diagnostic ultrasound on an unspecified date with unknown results. The patient recovered from the events on an unspecified date. Information about the lot/batch number has been requested.


VAERS ID: 1424661 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-02
Onset:2021-05-08
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-06-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM4965 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Heavy menstrual bleeding, Premature menopause, SARS-CoV-2 test
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (narrow), Immune-mediated/autoimmune disorders (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: DESOGESTREL
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021677660

Write-up: miscarriage; starting the menopause early; bleeding/very heavy menstrual bleed/ It went on for 2 weeks. This is very unusual for me, my periods last usually 5-7 days; This is a spontaneous report from a contactable consumer (patient) received from the Medicines and Healthcare products Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202106080831429220-8XYE8, Safety Report Unique Identifier GB-MHRA-ADR 25437786. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 02May2021 (batch/Lot Number: EM4965) as dose 1, single for covid-19 immunisation. Medical history included miscarriage from an unknown date and unknown if ongoing, contraception from an unknown date and unknown if ongoing. It was unsure if patient has had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. Concomitant medication included desogestrel taken for contraception start and stop date were not reported. The patient experienced miscarriage on an unspecified date and "bleeding/very heavy menstrual bleed/ It went on for 2 weeks. This is very unusual for me, my periods last usually 5-7 days" on 08May2021. The events were reported as serious (medically significant). The patient underwent lab tests and procedures which included COVID-19 virus test on unspecified date with No - Negative COVID-19 test result. The clinical course was reported as follows: after having the vaccine I had very heavy menstrual bleed. I was very concerned there was something seriously wrong, I thought I was either having a miscarriage (but I was not aware I was pregnant) or starting the menopause early. It went on for 2 weeks. This is very unusual for me, my periods last usually 5-7 days. Had I known this is a possible side effect I would have considered not getting the vaccine. I haven''t had another period yet so do not know if this is a long lasting issue. Patient has not tested positive for COVID-19 since having the vaccine. The outcome of the bleeding was recovered on 22May202. However, outcome of this event was also reported as "recovering". The event of miscarriage was recovered while unknown for the other event. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1471571 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-07
Onset:2021-05-08
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-07-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW6126 / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Asthenia, Fatigue, Haemorrhage, Hyperaesthesia, Myalgia, Pain of skin, Pregnancy test, Progesterone, Progesterone decreased
SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad), Sexual dysfunction (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: Medical History/Concurrent Conditions: Endometriosis; Pregnancy normal (proceeded normally and ended with the birth of a healthy child at 41 + 6 weeks of pregnancy.)
Allergies:
Diagnostic Lab Data: Test Date: 2021; Test Name: tests; Result Unstructured Data: Test Result:OK; Test Date: 20210602; Test Name: Progesterone; Result Unstructured Data: Test Result:16.7 nmol/L; Comments: very low
CDC Split Type: EEPFIZER INC2021804367

Write-up: pregnancy terminated spontaneously; bleeding; the level of progesterone was very lo/Progesterone analysis was performed: 16.7 nmol/l; Abdominal pain; muscle pain; Fatigue; weakness; Skin was sore/skin soreness; Hyperaesthesia; This is a spontaneous report from a contactable consumer downloaded from the regulatory authority-WEB report number EE-SAM-41982106144. This consumer reported information for both mother and fetus. This is the maternal report. A 32-year-old female patient received second dose of BNT162B2 (COMIRNATY), intramuscular on 07May2021 (Lot Number: EW6126) as 0.3 ml, single dose for covid-19 immunisation. Medical history included endometriosis from 2020, pregnancy from 2012 (proceeded normally and ended with the birth of a healthy child at 41 + 6 weeks of pregnancy). The patient''s concomitant medications were not reported. The patient previously took progesterone tablets for endometriosis in 2020. The patient was vaccinated with the second dose of Comirnaty vaccine on 07May2021. Next day on 08May2021 developed fatigue, weakness, muscle pain and the skin was sore. Patient also experienced hyperaesthesia on 08May2021. On 10May2021, the patient discovered that she was pregnant. On 04Jun2021, the pregnancy terminated spontaneously. All this time was abdominal pain. The tests were OK, only the level of progesterone was very low. Eventually, the fetal heart stopped and the pregnancy interrupted. The patient used paracetamol, ibuprofen, to treat the side effects. The condition was improving. She had no concomitant diseases, allergies, medications. Fatigue lasted for a few weeks, the rest (weakness, muscle pain and skin soreness) for 2-3 days. Abdominal pain was from 10May2021 to abortion on 04Jun2021. On 02Jun2021, the patient went emergency department due to bleeding. Progesterone analysis was performed: 16.7 nmol/l. Gepretix (progesterone) 1 capsule orally three times a day was prescribed. The size of the pregnancy at that time was 4 weeks, at the time of abortion (04Jun2021)-7 + 2. The patient took ibuprofen (600 mg x 3) when the pregnancy began to terminate (from June 4th), previously took paracetamol (1 g x 4) and drotaverine (80 mg x 2) due to pain. The previous pregnancy was in 2012, proceeded normally and ended with the birth of a healthy child at 41 + 6 weeks of pregnancy. There have been no abortions. In the autumn of 2020, progesterone tablets were prescribed because endometriosis was detected because the menstrual cycle was very painful. After a few months, everything returned to normal and the patient stopped treatment. The outcome of the event "pregnancy terminated spontaneously" was recovered on 04Jun2021, event abdominal pain was recovered on 04Jun2021, event muscle pain was recovered on 10May2021, event fatigue was recovered on 22May2021, event weakness was recovered on 10May2021, event hyperaesthesia was recovered on 10May2021, event "the level of progesterone was very lo/Progesterone analysis was performed: 16.7 nmol/l" was recovering, events "skin was sore/skin soreness" and bleeding was unknown. Sender Comment: Serious report due to miscarriage (medically significant). The initial side effects are known, the causal link is considered possible. Previous gynecological problems (endometriosis) may have contributed to the termination of the pregnancy. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : EE-PFIZER INC-2021881381 same product, reporter/ different patient (fetus case)


VAERS ID: 1477919 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-08
Onset:2021-05-08
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0193 / 1 RA / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Pregnancy test, Ultrasound scan, Vaccination site pain
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: MULTIVITAMIN [VITAMINS NOS]
Current Illness: Pregnant; Prenatal care
Preexisting Conditions: Medical History/Concurrent Conditions: Abstains from alcohol (during this pregnancy); Abstains from recreational drugs (during this pregnancy); Miscarriage; Multi gravida; Non-smoker (during this pregnancy); Para
Allergies:
Diagnostic Lab Data: Test Date: 20210521; Test Name: pregnancy blood test; Result Unstructured Data: Test Result:pregnant; Comments: pharmacy test; Test Date: 20210604; Test Name: abdominal echography; Result Unstructured Data: Test Result:showed foetal heart; Comments: 6 weeks of pregnancy (pregnancy intra uterine); Test Date: 202106; Test Name: abdominal echography; Result Unstructured Data: Test Result:absence of foetal heart; Comments: 9 weeks
CDC Split Type: CAPFIZER INC2021829833

Write-up: patient had spontaneous abortion/miscarriage/spontaneous miscarriage; vaccination site pain; The initial safety information received was reporting only non-serious adverse drug reactions, Upon receipt of follow-up information on 08Jul2021 this case now contains serious adverse reactions. Information processed together. This is a spontaneous report from two contactable nurses. A 41-year-old female pregnant patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), intramuscular, administered in the right arm on 08May2021 08:00 (batch/lot number EW0193 and expiry date 30Sep2021) at 41 years of age as dose 1, 0.3 ml single for covid-19 immunization. The patient''s medical history included prenatal and pregnancy; both ongoing. The patient''s first day of last menstrual period was on 12Apr2021 (due date 17Jan2022). The patient''s number of previous pregnancies was 4 and the number of other children is 1. The outcome of previous pregnancies was miscarriage. The reporter informed that the patient did not smoke, drink alcohol or use illicit drugs during this pregnancy. The patient has no previous vaccine (last 4 weeks), no other relevant medical history, no relevant family history, no test performed. Concomitant medications included vitamins nos (MULTIVITAMIN [VITAMINS NOS]) taken for prenatal and pregnancy from Jan2021 and ongoing. The patient knew she was pregnant via pharmacy test on 21May2021, she performed pregnancy blood test. The reporter informed that the patient was 28 days pregnant and experienced injection site pain (non-serious) on 08May2021 at 16:00. The patient received treatment of Advil due to the event. The reporter informed that the injection site pain lasted for 48 hours. The patient''s gestational period at time of initial exposure was 4 weeks, 1st trimester. The reporter informed that the patient had check-up on 04Jun2021 and had abdominal echography and the result was pregnancy intra uterine - 6 weeks evolution. The reporter informed that the patient had an echography at 6 weeks of pregnancy that showed foetal heart. At 9 weeks, patient re-did echography that showed an absence of foetal heart (Jun2021). The reporter informed that fetal heart stopped between 6 to 9 weeks of pregnancy. The patient received misoprolol intra-vaginal then expelled the fetus, no curettage required. The patient had spontaneous abortion/miscarriage (medically significant) with gestational period of 9 weeks (at termination) (Jun2021). The reason for termination was spontaneous miscarriage. The outcome of the event vaccination site pain was recovered on 10May2021, while patient had spontaneous abortion/miscarriage/spontaneous miscarriage was unknown.; Sender''s Comments: Based on the temporal relationship, the association between the event abortion with BNT162b2 can not be fully excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1358626 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-05-04
Onset:2021-05-09
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-05-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 038B21A / 1 LA / SYR
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 023C21A / 2 LA / SYR

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

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

Write-up: During the time of 1st dose dated:04/04/2021 didn''t knew I was pregnant. After second dose dated: 05/4/2021 we went for first scan on May 13th ,2021 and doctor suggested that the baby growth is not as per the weeks being calculated .They suggested that this might lead to miscarriage and asked us to come after 1 week date: 05/21/2021 .But soon after the visit I started noticing bleeding and spotting , we went back on Friday next week and there was no heart beat ,so they diagnosed it to be a miscarriage and gave medications following that. My blood reports and urine reports are normal. Wanted to report the event .


VAERS ID: 1399982 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: California  
Vaccinated:2021-04-14
Onset:2021-05-09
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-06-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Fatigue, Headache, Influenza like illness, Pain, Pregnancy test
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: 81mg aspirin
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: 5/3 and 5/4 at home hcg tests performed confirmed pregnancy. 5/9 hcg test performed by clinician confirmed there was no longer a pregnancy.
CDC Split Type:

Write-up: Chemical pregnancy experienced 3 weeks after 2nd shot in Moderna vaccination cycle. No reason to believe it was a related event, but reporting it nonetheless in case a trend emerges. Some flu-like symptoms (body aches, headache, fatigue) were experienced 24-48 hours after the shot but no fever.


VAERS ID: 1344928 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-05-09
Onset:2021-05-09
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Dizziness, Headache, Stillbirth
SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: OMEPRAZOLE
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Lactation decreased
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBMODERNATX, INC.MOD20211

Write-up: headache; i had my jab at 8: 12am; Light-headed; This regulatory authority case was reported by a consumer and describes the occurrence of HEADACHE (headache), STILLBIRTH (i had my jab at 8: 12am) and DIZZINESS (Light-headed) in a 41-year-old female patient who received mRNA-1273 (Moderna CoviD-19 Vaccine) for COVID-19 vaccination. The patient''s past medical history included Lactation decreased. Concomitant products included OMEPRAZOLE from 05-Apr-2021 to an unknown date for Acid indigestion. On 09-May-2021, the patient received first dose of mRNA-1273 (Moderna CoviD-19 Vaccine) (unknown route) 1 dosage form. On 09-May-2021, the patient experienced DIZZINESS (Light-headed) (seriousness criterion medically significant). On an unknown date, the patient experienced HEADACHE (headache) (seriousness criterion medically significant) and STILLBIRTH (i had my jab at 8: 12am) (seriousness criterion medically significant). At the time of the report, HEADACHE (headache), STILLBIRTH (i had my jab at 8: 12am) and DIZZINESS (Light-headed) was resolving. The action taken with mRNA-1273 (Moderna CoviD-19 Vaccine) (Unknown) was unknown. She had her jab at 8:12am, she felt fine afterwards. Around 2:30pm she started to feel a little odd, light headed/dizzy/drunk almost and a few hours after she had a fuzzy headache. she rang 111 who advised a doctor would call her back, in the meantime she increased her fluids intake, took two paracetamols and rested. The doctor told her to keep doing as she was and that the symptoms should ease, if they were still apparent after 3 days. She need to contact her doctor. Patient had not tested positive for COVID-19 since having the vaccine. Company Comment: This is a case of product exposure during pregnancy (unknown gestational age) with stillbirth for this 41-year-old female. . For the other events such as headache and dizziness a causal relationship cannot be excluded. Very limited information regarding this events has been provided at this time. No follow up is possible.; Sender''s Comments: This is a case of product exposure during pregnancy (unknown gestational age) with stillbirth for this 41-year-old female. . For the other events such as headache and dizziness a causal relationship cannot be excluded. Very limited information regarding this events has been provided at this time. No follow up is possible.


VAERS ID: 1352423 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-23
Onset:2021-05-09
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-05-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER9449 / UNK - / -

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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021529866

Write-up: Early miscarriage; This is a Non-Interventional Study report from a contactable consumer. This is a report received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-YCVM-202104271057312980-HZU2Y. Safety Report Unique Identifier GB-MHRA-ADR 25273130. A 41-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 23Apr2021 (Lot Number: ER9449) as single dose for COVID19 immunisation. Medical history was not reported. Patient last menstrual period date: 21Mar2021. Estimated due date: 26Dec2021. Concomitant medication included folic acid taken for Folic acid supplementation. Patient had not had symptoms associated with COVID-19. Not had a COVID-19 test. Patient was not enrolled in clinical trial. Patient was not currently breastfeeding. The patient experienced early miscarriage on 09May2021. The events were reported as serious, hospitalization, medically significant, congenital anomaly. The mother reported she became pregnant while taking bnt162b2. The mother was 7 Weeks pregnant at the onset of the event. The patient was due to deliver on 26Dec2021. Patient had not tested positive for COVID-19 since having the vaccine. Patient did think vaccination had an adverse effect on the pregnancy. Pregnancy adverse effects details: Death of embryo. Details of previous pregnancies: Pregnancy was unknown at time of vaccination. Patient was exposed to the vaccine Unknown. The patient told she was possibly pregnant as her period was a bit late but she wasn''t sure as she hadn''t tested, and she was told it was ok. It wasn''t. The outcome of event Early miscarriage was not recovered. The reporter''s assessment of the causal relationship of the event with the suspect product was not provided at the time of this report. Since no determination has been received, the case is managed based on the company causality assessment. No follow up attempts are possible. No further information is expected.; Sender''s Comments: The event of Early miscarriage is assessed as possibly related to the suspect vaccine(BNT162B2) based on strong temporal association, but consider also possible contributory effects from patient''s medical history and/or concomitant medications. "The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate."


VAERS ID: 1355847 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-11
Onset:2021-05-09
   Days after vaccination:59
Submitted: 0000-00-00
Entered: 2021-05-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain lower, Abortion spontaneous, Haemorrhage, Pregnancy test, SARS-CoV-2 test, Ultrasound scan vagina
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Termination of pregnancy and risk of abortion (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? 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: Asthma; Pregnancy (Patient no longer pregnant at the time of reporting).
Allergies:
Diagnostic Lab Data: Test Name: pregnancy test; Result Unstructured Data: Test Result: Positive; Test Date: 20210106; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:Yes - Positive COVID-19 test; Test Name: Bloods Trans Vaginal scan; Result Unstructured Data: Test Result: Pregnancy of Unknown Location positive HCG unknown.
CDC Split Type: GBPFIZER INC2021535066

Write-up: low abdominal pain with heavy bleeding; low abdominal pain with heavy bleeding; Miscarriage; This is a spontaneous report from a contactable consumer received from the Medicines and Healthcare products Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202105111054182360-U7PDH, and Safety Report Unique Identifier GB-MHRA-ADR 25278062. An 18-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 11Mar2021 (Batch/Lot number was not reported) at 1st dose, single for COVID-19 immunisation. Medical history included pregnancy (patient no longer pregnant at the time of reporting), and asthma. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Concomitant medication included folic acid. The patient experienced miscarriage on 09May2021 with outcome of not recovered, low abdominal pain with heavy bleeding on an unspecified date with outcome of unknown. The event miscarriage was assessed as serious, congenital anomaly by health authority. The patient underwent lab tests and procedures which included COVID-19 virus test: Yes - Positive COVID-19 test on 06Jan2021, Bloods Trans Vaginal scan: Pregnancy of Unknown Location positive HCG unknown gestation on an unspecified date, pregnancy test: positive on an unspecified date. The clinical course was reported as follows: Low abdominal pain with heavy bleeding, Positive pregnancy test at hospital, unknown conception as on oral contraceptive. Did the medicine have an adverse effect on any aspect of the pregnancy: Yes. Pregnancy adverse effects details: Miscarriage. Patient did not take folic acid supplement during pregnancy. Details of previous pregnancies: NIL. Patient was exposed to the medicine before pregnancy (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.


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