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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: 1872508 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Puerto Rico  
Vaccinated:2021-02-01
Onset:2021-02-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-11-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Allergy to vaccine, Discomfort, Fatigue, Headache, Maternal exposure before pregnancy, Pruritus, Rash macular, Somnolence, Tenderness, Vaccination site erythema, Vaccination site pain, Vaccination site swelling
SMQs:, Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20213

Write-up: miscarriage at week 14; sleepiness; heaviness; spots on face/spots on breast area/spots on face arms (ongoing); itching; tenderness in arm; arm discomfort/ pain in the arm; swelling in the arm/swelling; redness in the arm; allergic reaction after doses 1 and 2, three days after the doses were administered; tiredness; headache; pregnant after the vaccine; This spontaneous retrospective pregnancy case was reported by a consumer and describes the occurrence of ABORTION SPONTANEOUS (miscarriage at week 14) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. In February 2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In March 2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. Last menstrual period and estimated date of delivery were not provided. In February 2021, the patient experienced MATERNAL EXPOSURE BEFORE PREGNANCY (pregnant after the vaccine). On an unknown date, the patient experienced ABORTION SPONTANEOUS (miscarriage at week 14) (seriousness criterion medically significant), VACCINATION SITE PAIN (arm discomfort/ pain in the arm), SOMNOLENCE (sleepiness), VACCINATION SITE SWELLING (swelling in the arm/swelling), VACCINATION SITE ERYTHEMA (redness in the arm), DISCOMFORT (heaviness), RASH MACULAR (spots on face/spots on breast area/spots on face arms (ongoing)), PRURITUS (itching), TENDERNESS (tenderness in arm), ALLERGY TO VACCINE (allergic reaction after doses 1 and 2, three days after the doses were administered), FATIGUE (tiredness) and HEADACHE (headache). The vaginal delivery occurred on 30-Sep-2021, which was reported as Spontaneous Abortion. For foetus 1, The outcome was reported as Spontaneous Abortion NOS. In February 2021, MATERNAL EXPOSURE BEFORE PREGNANCY (pregnant after the vaccine) had resolved. At the time of the report, ABORTION SPONTANEOUS (miscarriage at week 14), VACCINATION SITE PAIN (arm discomfort/ pain in the arm), SOMNOLENCE (sleepiness), VACCINATION SITE SWELLING (swelling in the arm/swelling), VACCINATION SITE ERYTHEMA (redness in the arm), DISCOMFORT (heaviness), RASH MACULAR (spots on face/spots on breast area/spots on face arms (ongoing)), PRURITUS (itching), TENDERNESS (tenderness in arm), ALLERGY TO VACCINE (allergic reaction after doses 1 and 2, three days after the doses were administered), FATIGUE (tiredness) and HEADACHE (headache) outcome was unknown. Concomitant medications were not provided Treatment information was not provided. This case concerns a female patient of unknown age with no relevant medical history reported, who experienced the unexpected, serious (medically significant) event of abortion spontaneous at 14 weeks of gestational age. The patient was exposed to the vaccine before getting pregnant. The event of abortion spontaneous occurred approximately 7 months after the first dose of mRNA-1273 and 6 months after the second dose of mRNA-1273. The rechallenge was not applicable since the events occurred after the second dose. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to MOD-2021-378007 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 08-Nov-2021: Significant follow up document received on 08-Nov-2021 contains new events, hence added and updated.; Sender''s Comments: This case concerns a female patient of unknown age with no relevant medical history reported, who experienced the unexpected, serious (medically significant) event of abortion spontaneous at 14 weeks of gestational age. The patient was exposed to the vaccine before getting pregnant. The event of abortion spontaneous occurred approximately 7 months after the first dose of mRNA-1273 and 6 months after the second dose of mRNA-1273. The rechallenge was not applicable since the events occurred after the second dose. The benefit-risk relationship of mRNA-1273 is not affected by this report.


VAERS ID: 1070340 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-14
Onset:2021-02-01
Submitted: 0000-00-00
Entered: 2021-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Asthenia, Headache, Pruritus, Swelling, Vaginal haemorrhage
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemorrhage terms (excl laboratory terms) (narrow), Guillain-Barre syndrome (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Abortion; Pregnancy loss
Allergies:
Diagnostic Lab Data:
CDC Split Type: ILPFIZER INC2021141461

Write-up: Weakness; headache; Swelling in the armpit; little but of itching in the abdomen and chest area (without rash); Vaginal bleeding started which that finally ended in a natural miscarriage; Vaginal bleeding; This is a spontaneous report from a contactable consumer (patient) via the reception desk. A 36-year-old pregnant female patient received the second dose of BNT162B2 ( PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: not reported), via an unspecified route of administration, on 14Feb2021 at single dose for COVID-19 immunisation. Medical history included had a pregnancy loss after a pulse wasn''t developed during the 8 week and had to do an abortion from an unknown date. The patient''s concomitant medications were not reported. The patient previously received the first dose of BNT162B2 on 20Jan2021 (lot number: not reported) for COVID-19 immunization. It was reported that patient was a mother of two girls. The patient was pregnant in a very early week 5. On 20Jan2021, the patient received the first dose of the vaccine. The patient was supposed to receive second dose of vaccination on 11Feb2021. The patient was afraid from the influence of the second vaccine during such an early stage of pregnancy. The patient need clarification regarding second dose of vaccination whether it can be taken in the fifth week of the pregnancy or wait until second trimester. The patient referred to a gynaecologist, internist in the corona department and also to infectiology physician. From them patient understood that there can be spaced between the first and second vaccine to a period of up to 6 weeks and afterwards, the efficiency of the vaccine would damage. It was also reported that a period of 6 weeks between the first and second dose means week 7-8 of pregnancy, still in the first sensitive first trimester. The patient was under medical supervision and everything was normal. After consultation with gynaecologist, internist and infectiology, the patient was not sure regarding the date of the second dose. The patient was explained that there was no information or recommendation regarding pregnancy and the vaccination against corona. She should receive medical guidance from her treating physician who was treating her and knows her medical background. It was explained that delay of the second dose beyond the recommended times could damage the results of the vaccine, but she should consult her physician and to receive the decision with them regarding the time of the second dose. The patient was suggested to consult and review the instructions of the agency regarding vaccination of pregnant women in the first trimester. It was reported that patient was interested to receive the second dose of the vaccine because she sees a great importance to the vaccine and protection from it. On 18Feb2021, it was reported that the patient did the second vaccination on 14Feb2021 and about 18 hours after, on Feb2021, vaginal bleeding started which that finally ended in a natural miscarriage. The patient also experienced weakness, headache, swelling in the armpit and a little but of itching in the abdomen and chest area (without rash) on an unspecified date. The patient does not know if this was related to the vaccination or "to the rare danger storm" but felt the need to update. The patient reported that she had another miscarriage due to non-development, no pulse was detected before the vaccination. Patient consulted with gynecologists, researchers of the biology field, infectiology experts and internists and everyone consulted her to be vaccinated with the second dose during the first trimester and she was vaccinated from risk management and from understanding that this is important. The outcome of the events was unknown. Information on the lot/batch number has been requested. Follow up (18Feb2021): New information was received from the same reporting consumer includes: dosing regimen, new events (vaginal bleeding started which that finally ended in a natural miscarriage, weakness, headache, swelling in the armpit and a little but of itching in the abdomen and chest area (without rash)). Information on the lot/batch number has been requested.


VAERS ID: 1131164 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-02-01
Submitted: 0000-00-00
Entered: 2021-03-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: ITPFIZER INC2021135369

Write-up: internal abortion (unfortunately the embryo was not growing). I was at the ninth week but the size was still that of a embryo of 4 weeks; (unfortunately the embryo was not growing). I was at the ninth week but the size was still that of a embryo of 4 weeks; This is a spontaneous reported through the WEB Pfizer program from a contactable consumer (patient). This female patient of unspecified age received BNT162B2 (COMIRNATY) at single dose for COVID-19 immunization, the first dose was on 13Jan2021, the second dose was on an unspecified date. Medical history and concomitant medications were not reported. The patient received the two doses of the covid vaccine and found out to be pregnant. She enquired if there was a way to get inserted into the experimentation, as she would like to help other mothers with my pregnancy data. Patient reported she lost her baby about three weeks ago in Feb2021 due to internal abortion (unfortunately the embryo was not growing). She was at the ninth week, but the size was still that of an embryo of 4 weeks. Last cycle date was 14Dec2020. Obviously patient was aware of the impossibility of identifying a causal link. The outcome of event was unknown. Follow-up (12Mar2021): New information reported from the same contactable consumer includes: event term updated; vaccine product details. This case upgraded to serious now.


VAERS ID: 1161744 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2021-02-17
Onset:2021-02-01
Submitted: 0000-00-00
Entered: 2021-04-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Foetal death, Foetal heart rate abnormal, Foetal movement disorder, Histology, Laboratory test, Prenatal screening test, Syndactyly, X-ray
SMQs:, Congenital, familial and genetic disorders (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: histological check of the placenta; Result Unstructured Data: Test Result:unknown; Test Name: genetic test; Result Unstructured Data: Test Result:unknown; Test Name: integrated test; Result Unstructured Data: Test Result:normal; Test Name: x- ray; Result Unstructured Data: Test Result:Unknown results
CDC Split Type: ILPFIZER INC2021348948

Write-up: IUFD; did not feel fetal movement; no fetal heart beat; syndactyly in fingers 4-5 in the right leg; This is a spontaneous report received from a contactable other HCP via Regulatory Authority. This other hcp reported information for both mother and fetus. This is a fetus report. A fetus patient of an unspecified gender received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), first dose transplacental on 17Feb2021, single dose for covid-19 immunisation. The patient''s medical history and concomitant medications were not reported. The day before injection on 17Feb2021 received the first injection of the vaccine for COVID 19 in a community setting. When mother was given it there was no fetal heart beat. In an ultrasound check it showed a fetus with no heartbeat and no movement, IUFD. PCR test for COVID 19 when she was admitted was negative. The mother gave birth on date in the evening and the fetus was without external birth defects except for syndactyly in fingers 4-5 in the right leg. Even with request and repeated explanation, the woman refused an autopsy but agreed to a genetic test, x-rays, medical photographs and histological check of the placenta in addition to a corona test from the placenta and from the fetus.The outcome of the event IUFD was fatal, unknown for other events. No follow-up attempts possible. No further information expected.; Sender''s Comments: The reported events IUFD, fetal movement disorder, fetal heart rate absent and syndactyly are likely an intercurrent condition and not related to bnt162b2 .; Reported Cause(s) of Death: IUFD


VAERS ID: 1188982 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-18
Onset:2021-02-01
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-04-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6788 / 1 - / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Crohn''s disease
Allergies:
Diagnostic Lab Data:
CDC Split Type: FRPFIZER INC2021333700

Write-up: Early miscarriage; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority-WEB FR-AFSSAPS-MA20210840. A 29-year-old pregnant female patient received the first dose of BNT162b2 (COMIRNATY, Lot Number: EJ6788) via intramuscular route on 18Jan2021 (at the age of 28-years-old) as a single dose for COVID-19 immunization. The patient''s medical history included Crohn''s disease from an unspecified date and unknown if ongoing. There was no information on the patient''s obstetrical history. The patient did not have a history of COVID-19. Concomitant medications were not reported. On 01Feb2021, the patient had an early miscarriage, 14 days after the first dose of COMIRNATY, which required hospitalization. Discovery of pregnancy was 1 week after the first dose of vaccine. The spontaneous miscarriage occurred at 5 weeks of amenorrhea. The outcome of spontaneous miscarriage was reported as recovered on unspecified date. No follow-up attempts possible. No further information expected.


VAERS ID: 1265256 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-01
Onset:2021-02-01
   Days after vaccination:31
Submitted: 0000-00-00
Entered: 2021-04-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, SARS-CoV-2 test, Scan, Terminal insomnia
SMQs:, Depression (excl suicide and self injury) (broad), 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: Folic acid supplementation; Lactation decreased; Miscarriage; Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Date: 20210412; Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test; Test Date: 202102; Test Name: Scan; Result Unstructured Data: Test Result:missed miscarriage; Comments: missed miscarriage at 10 weeks after receiving both doses of the vaccine in early pregnancy
CDC Split Type: GBPFIZER INC2021404986

Write-up: Maternal exposure during pregnancy; Awakening early; Early miscarriage; This is a spontaneous report from a contactable consumer or other non hcp received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202104121547170060. Safety Report Unique Identifier: GB-MHRA-ADR 25126242. A 36-year-old female patient received second dose of BNT162B2 (COVID-19 MRNA VACCINE BIONTECH, Solution for injection), via an unspecified route of administration on Jan2021 as single dose for COVID-19 immunisation. Medical history included, Miscarriage, pregnancy from 2019 (Patient no longer pregnant at the time of reporting), suppressed lactation, and Folic acid supplementation. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Historical vaccine included first dose BNT162B2 (COVID-19 MRNA VACCINE BIONTECH, Solution for injection), via an unspecified route of administration on Dec2020 as single dose for COVID-19 immunisation. Patient has not had symptoms associated with COVID-19. Concomitant medication(s) included folic acid at 400 ug for vitamin supplementation. The patient reported, she received the COVID vaccine in Dec when she was very early pregnant and did not know she was pregnant. She then subsequently had the second dose after 3 weeks, at this point she knew that she was pregnant but chose to continue to have the vaccine. She then suffered a miscarriage in Feb2021 when she was 10 week pregnant and had to undergo a removal of products. She don''t know whether this was related to the vaccine at all, and was sure will never know but she thought that she should report it. Patient was exposed to the medicine first-trimester (1-12 weeks). The patient experienced early miscarriage on Feb2021; awakening early and maternal exposure during pregnancy on an unknown date. The mother reported she became pregnant while taking BNT162B2. The patient underwent lab tests and procedures which included COVID-19 virus test Negative on 12Apr2021, scan showed missed miscarriage at 10 weeks after receiving both doses of the vaccine in early pregnancy on Feb2021. Patient has not tested positive for COVID-19 since having the vaccine. Outcome of event for early miscarriage was recovered on an unspecified date in Feb2021, for awakening early was recovering and for maternal exposure during pregnancy was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1276133 (history)  
Form: Version 2.0  
Age: 41.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-01
Onset:2021-02-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6795 / 2 - / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: COVID-19 (disease symptoms: quite)
Allergies:
Diagnostic Lab Data: Test Date: 20200314; Test Name: corona, confirmed with test; Test Result: Positive
CDC Split Type: NLPFIZER INC2021414285

Write-up: Miscarriage; Vaccination during pregnancy; This is a spontaneous report from a contactable consumer downloaded from the Regulatory Authority-WEB, regulatory authority number NL-LRB-00504559. A 41-year-old female patient received bnt162b2 (COMIRNATY, Batch/Lot Number: EJ6795), dose 2 intramuscular on 01Feb2021 (at the age of 41years) as single dose for Covid-19 immunization. The patient received the first dose of Comirnaty on an unspecified date for Covid-19 immunization. The patient reported that she was not pregnant at the first administration. Medical history included Covid-19 from 14Mar2020 to an unknown date (disease symptoms: quite). The patient''s concomitant medications were not reported. It was reported that the patient had a miscarriage (other medically important condition), on 08Apr2021 also reported as 9 weeks after exposure to Covid-19 vaccine Pfizer injection. The miscarriage occurred at a pregnancy duration of 12.5 weeks. The (second) vaccination took place at a pregnancy duration of 3.5 weeks. The patient reported that she does not know whether the miscarriage was related to the vaccination, at 8 weeks there was still a beating heart (miscarriage was 4-5 weeks after the 2nd vaccination). The outcome of events was unknown. No follow-up attempts are possible. No further information is expected. Information on lot number already obtained.


VAERS ID: 1021115 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: New York  
Vaccinated:2020-12-23
Onset:2021-02-02
   Days after vaccination:41
Submitted: 0000-00-00
Entered: 2021-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: TV US on 2/10 showing missed miscarraige of twins
CDC Split Type:

Write-up: I found out I was pregnant between dose 1 and 2 of the vaccines. I received dose 1 on 12/23/21 and had a positive pregnancy test on 1/2/21. I had my 2nd dose on 1/13 at 5w6 days based on LMP. I had my first prenatal visit on 2/10/21 at which time US showed twin gestation but neither fetus had a heartbeat.


VAERS ID: 1069793 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: New York  
Vaccinated:2021-01-08
Onset:2021-02-02
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012L20A / 1 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Haemorrhage, Headache, Ultrasound pelvis, Uterine dilation and curettage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow)

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

Write-up: 1/8 vaccination HA went away after a week bleeding in between vaccinations ultra sounds weekly, blood work 1st went to ER, 2nd bleeding episode went to PCM for same day visit 2/2 miscarriage, D&C


VAERS ID: 1174856 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-06
Onset:2021-02-02
   Days after vaccination:27
Submitted: 0000-00-00
Entered: 2021-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6797 / 1 - / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID; IODINE
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210126; Test Name: gynecological test; Result Unstructured Data: Test Result:intrauterine bleeding, regular contours; Comments: intrauterine bleeding, regular contours, embryo compatible with 6 weeks, no heartbeat
CDC Split Type: PTPFIZER INC2021317769

Write-up: spontaneous abortion; This is a spontaneous report from a contactable physician downloaded from an Agency -WEB, regulatory authority number PT-INFARMED-B202103-1998. A 42-year-old female patient received bnt162b2 (COMIRNATY), dose 1 intramuscular on 06Jan2021 (Batch/Lot Number: 1st dose: EJ6797) as 0.3 mL, single for covid-19 immunisation. Medical history was not reported. The patient was unaware of pregnancy when the first dose of the vaccine was administered. Concomitant medication included folic acid taken for an unspecified indication, start and stop date were not reported; iodine taken for an unspecified indication, start and stop date were not reported. Twenty days after the administration of the first dose of the vaccine, with amenorrhea of 7/8 weeks, the patient underwent a gynecological test. An embryo compatible with 6 weeks was found, with regular contours, without visualization of heartbeat. In the following week (27 days after the first dose of the vaccine was administered), hemorrhage was observed. After examination, it was concluded that spontaneous abortion had occurred. Misoprostol, 2 micrograms, was administered vaginally. After the abortion, the patient received the 2nd dose of the vaccine to complete the vaccination scheme. Patient notes: On 26Jan2021: amenorrhea of 7/8 weeks. On 26Jan2021: gynecological test - intrauterine bleeding, regular contours, embryo compatible with 6 weeks, no heartbeat. On 02Feb2021: reference to hemorrhage. Misoprostol, 2 micrograms, was administered vaginally. On 09Feb2021: discharge of the appointment. The outcome of the event was not recovered. No follow-up attempts needed. No further information expected.


VAERS ID: 1235258 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-02
Onset:2021-02-02
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLPFIZER INC2021370895

Write-up: had a miscarriage, 5 weeks after administration of covid-19 vaccine Pfizer; had a miscarriage, 5 weeks after administration of covid-19 vaccine Pfizer; This is a spontaneous report from a contactable consumer downloaded from the Regulatory Authority-WEB, regulatory authority number is NL-LRB-00491493. A 27-year-old female patient received BNT162B2 (COMIRNATY, solution for injection), dose 2 via an unspecified route of administration on 02Feb2021 (Batch/Lot Number: Unknown) at single dose (at the age of 27 years old) for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously took COMIRNATY, dose 1 on 10Jan2021 for COVID-19 immunisation and experienced maternal exposure during pregnancy. On 09Mar2021, the patient had a miscarriage (other medically important condition), 5 weeks after administration of covid-19 vaccine Pfizer. It was her second vaccination on 02Feb2021. The pregnancy duration is unknown. The outcome of the event was unknown. Sender''s Comment: Since the nature of the reported reaction does imply seriousness according to the critera, the reaction (Miscarriage) was considered as serious. No follow-up attempts are possible; information on batch number cannot be obtained.; Sender''s Comments: Linked Report(s) : NL-PFIZER INC-2021415067 same patient, same drug, similar event, different dose


VAERS ID: 1852123 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-02
Onset:2021-02-02
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-11-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL8723 / 2 RA / -

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

Life Threatening? No
Birth Defect? 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: ESPFIZER INC202101437931

Write-up: Termination of pregnancy - medical; Maternal condition affecting foetus; Last dose of vaccine administered on 02Feb2021; pregnancy achieved in the first week of March 2021; This is a spontaneous report from a contactable consumer (patient, also reported as a nurse, currently (as of 25Oct2021) statutory staff in a vacant position in the Internal Medicine service) downloaded from the Regulatory Authority, regulatory authority number ES-AEMPS-941552. This consumer reported information for both mother and fetus/baby. This is a maternal report. Both cases were serious. A 30-years-old female patient received 2nd dose of bnt162b2 (COMIRNATY), at single dose via an unspecified route of administration, administered in right arm on 02Feb2021 (Lot Number: EL8723) at 30-years-old for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient had no passed COVID-19. Historical vaccine included 1st dose of BNT162B2 (COMIRNATY) in right arm on 10Jan2021 (Lot number EM0477) for covid-19 immunization. The reported events were termination of pregnancy - medical with onset date of 07Jul2021, maternal condition affecting foetus with onset date of 02Feb2021; both with seriousness criteria of medically significant. The mother was not pregnant on vaccine administration; she became pregnant after taking bnt162b2. Pregnancy achieved in the first week of Mar2021. The mother was 18 weeks pregnant at the onset of the event. The clinical course was reported as follows: Severe congenital heart disease in pregnancy occurring 4 weeks after vaccination. At 18 weeks of gestation (07Jul2021), termination of pregnancy due to presenting the fetus Heterotaxia with Hypoplasia of the Left Ventricle and absence of left atrium, absence of inferior vena Cava and transposition of vessels. Fetal abdominal inversus situsus. Fetus currently (as of 25Oct2021) awaiting autopsy and pathological anatomy. Outcome of the events was unknown. The reporter would like to provide all the necessary data and allow access to everything necessary to check if there has been any type of relationship between vaccination and the fatal outcome of pregnancy. No follow up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : 202101466841 Same product and dose, different event and patient


VAERS ID: 1028819 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Missouri  
Vaccinated:2020-12-18
Onset:2021-02-03
   Days after vaccination:47
Submitted: 0000-00-00
Entered: 2021-02-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL1284 / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Foetal heart rate abnormal, Human chorionic gonadotropin decreased, 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), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Wellbutrin, Zyrtec, Benadryl, flexeril, prenatal vitamins.
Current Illness: None
Preexisting Conditions: Anxiety, migraines
Allergies: Latex, PCN, sulfa, reglan, phenergan
Diagnostic Lab Data: 2/3 - ultrasound showed no heartbeat 2/5 - beta hcg quant - 41,xxx 2/7 - beta hcg quant - 40,xxx 2/11 - 2nd confirmation ultrasound. 2/11 - beta hcg quant - 35,xxx
CDC Split Type:

Write-up: First trimester miscarriage after receiving both vaccine doses while pregnant. Granada 5, Para 3 at time of vaccine administration. Due date 9/17/2021


VAERS ID: 1047536 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Delaware  
Vaccinated:2021-02-02
Onset:2021-02-03
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 AR / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Fatigue, Human chorionic gonadotropin decreased, Injection site pain, Lethargy, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Tylenol on day 2 after vaccination
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Received vaccine on 02/02, 4 weeks pregnant on 02/03 02/03-02/05: Severe lethargy, tiredness, pain at injection sites, fever all lasting 48 hours. Symptoms subsided after taking tylenol on 02/05. I''m not attributing this to the vaccine, but on 02/12, my hcg started to plateau and decline, no egg yolk or fetal pole was seen at 6 weeks (2/17). Sac was measuring at 5 weeks. I eventually had a miscarriage on 2/21


VAERS ID: 1047642 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-02-01
Onset:2021-02-03
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Blood pressure increased, Exposure during pregnancy, Headache, Induced labour, Infection, Pre-eclampsia, Premature delivery, Protein urine present, Pulmonary haemorrhage
SMQs:, Acute renal failure (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Hypertension (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Chronic kidney disease (broad), Proteinuria (narrow), Tubulointerstitial diseases (broad), 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? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Pantaprazole for heartburn from pregnancy, prenatal daily vitamin, 1000 IU vitamin D
Current Illness: None. Had a normal pregnancy. Had pregnancy heartburn that was normal.
Preexisting Conditions: None. Had occasional pre hypertension prior to pregnancy but never treated for it.
Allergies: Noneq
Diagnostic Lab Data: I believe I had slightly elevated protein in my urine 2/8. My blood pressure go to be 160/118 or so I think, even with medication.
CDC Split Type:

Write-up: I began having headaches nightly 2 nights after my second dose. On 2/7 my blood pressure was about 135/90. On 2/9 my blood pressure was 150/90 or 95 and then it increased by the time I went to my doctor?s office that afternoon. I had severe pre eclampsia on 2/8 and was induced and delivered 2/9 with a 34 week old baby. She had an infection and pulmonary hemorrhage.


VAERS ID: 1063163 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-01-19
Onset:2021-02-03
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-03-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 028L20A / 2 RA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: PRENATAL, VITAMIN D, B COMPLEX
Current Illness:
Preexisting Conditions: ANXIETY, MIGRAINES, IBS
Allergies:
Diagnostic Lab Data: Ultrasound - Feb 3
CDC Split Type:

Write-up: Saw OB on Jan 4 and there was a strong heartbeat and no defects or problems noted in any bloodwork up to that point in the pregnancy. Received my second vaccine on Jan 19. On Feb 3 I went to my next ultrasound appointment and was told that the baby had no heartbeat. It was estimated that the baby had likely passed a couple weeks prior but I am not certain of the timeline in regards to receiving the second vaccine.


VAERS ID: 1074063 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2020-12-27
Onset:2021-02-03
   Days after vaccination:38
Submitted: 0000-00-00
Entered: 2021-03-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 RA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unithroid - thyroid medication; multivitamin
Current Illness: No
Preexisting Conditions: History of papillary thyroid cancer; hypothyroidism, post surgical
Allergies: NKDA
Diagnostic Lab Data: Follow up ultrasound following complete spontaneous abortion
CDC Split Type:

Write-up: Miscarriage, first trimester


VAERS ID: 1440957 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Georgia  
Vaccinated:2021-02-03
Onset:2021-02-03
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 UN / UN
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 030L20A / 2 UN / UN

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Anembryonic gestation, Haemoglobin normal, Maternal exposure during pregnancy, Pregnancy test urine positive, Progesterone decreased, 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), Normal pregnancy conditions and outcomes (narrow), Sexual dysfunction (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? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Urine pregnancy test positive 5/24/21; Progesterone 9, 6/10/21; O positive, 6/21/21; Hgb 12.5, 6/21/21
CDC Split Type:

Write-up: Miscarriage occurred during 1st pregnancy since the vaccine. LMP April 6, 2021, diagnosis of blighted ovum on June 17, 2021. D&C on June 22, 2021.


VAERS ID: 1158739 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-14
Onset:2021-02-03
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-04-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ1688 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Decreased embryo viability, Haemorrhage in pregnancy, Ultrasound scan
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: COVID-19 virus test negative; In vitro fertilisation (previous successful pregnancy through IVF due to male factor infertility (low sperm count, mobility, and quality)); Pregnancy (2 previous pregnancies); Suspected COVID-19
Allergies:
Diagnostic Lab Data: Test Date: 20210226; Test Name: Ultrasound scans; Result Unstructured Data: Test Result:twin pregnancy, very early remnants in one sac and; Comments: embryo of 6 weeks in age in other sac; Test Date: 20210308; Test Name: Ultrasound scans; Result Unstructured Data: Test Result:most developed embryo reducing in size with each; Comments: week; Test Date: 20210315; Test Name: Ultrasound scans; Result Unstructured Data: Test Result:most developed embryo reducing in size with each; Comments: week
CDC Split Type: GBPFIZER INC2021300860

Write-up: early miscarriage; embryo reducing in size with each week; Spotting; This is a spontaneous report from a contactable consumer received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202103161328406440, Safety Report Unique Identifier is GB-MHRA-ADR 24956506. A pregnant female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EJ1688) via an unspecified route of administration on 14Jan2021 at a single dose for COVID-19 immunisation. Medical history included 2 previous pregnancies; previous successful pregnancy through IVF due to male factor infertility (low sperm count, mobility, and quality). The patient also had suspected COVID-19 from 10Dec2020 to 18Dec2020, but it was also reported that patient had negative COVID-19 virus test on 12Dec2020. Patient is not enrolled in clinical trial. The patient was pregnant at the time of the vaccination. Concomitant medication included folic acid taken for pregnancy from 01Nov2020 (as reported). First day of last period was 27Dec2020. The patient started spotting on 03Feb2021. Ultrasound scan on 26Feb2021 revealed twin pregnancy, very early remnants in one sac and embryo of 6 weeks in age (as reported) in other sac. Confirmed on further ultrasound scans on 08Mar2021 and 15Mar2021 (most developed embryo reducing in size with each week). Surgical management was done to remove pregnancy tissue on 15Mar2021. The patient had early miscarriage on unspecified date. The outcome of the early miscarriage was recovered with sequel, while for the other events was recovered. The case has been considered serious due to congenital anomaly. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1331346 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-03
Onset:2021-02-03
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion missed, Headache, Musculoskeletal pain, Pyrexia, Ultrasound scan
SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Allergic reaction to analgesics; Penicillin allergy
Allergies:
Diagnostic Lab Data: Test Date: 20210226; Test Name: monitoring ultrasound; Result Unstructured Data: Test Result:absence of a fetal heartbeat; Comments: fetal heartbeat was observed, diagnosing a missed abortion and proceeding with curettage, without incident
CDC Split Type: ESPFIZER INC2021496710

Write-up: missed abortion; fever; arthromyalgia; headache; This is a spontaneous report from a contactable physician downloaded from the WEB [ES-AEMPS-846901]. A 36-year-old female patient received bnt162b2 (COMIRNATY), intramuscular on 03Feb2021 (Batch/Lot Number: Unknown) as 2nd dose, 0.3 single for covid-19 immunisation. Medical history included allergy to metamizole and penicillin. Concomitant medications were not reported. Historical vaccine included first dose of Comirnaty on Jan2021 for covid-19 immunisation and experienced asthenia and chills. On 03Feb2021, the patient was presented with fever, arthromyalgia and headache. Afterward, on 15Feb2021, the patient discovered that she was pregnant. On 26Feb2021 (9th week of gestation) a monitoring ultrasound was performed and the absence of a fetal heartbeat, diagnosing a missed abortion and proceeding with curettage, without incident. The patient recovered from the event abortion on 26Feb2021. The outcome of other events was unknown. No follow-up attempts are possible. No further information expected. Information on batch/lot number cannot be obtained.; Sender''s Comments: Linked Report(s) : ES-PFIZER INC-2021534245 same patient, different dose


VAERS ID: 1866405 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-02
Onset:2021-02-03
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-11-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion induced, Pain in extremity, Pruritus, SARS-CoV-2 test
SMQs:, Anaphylactic reaction (broad), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Bariatric surgery (I take vitamins after bariatric surgery); DVT (deep vein thrombosis); Epilepsy (I have epilepsy in remission on Tegretol slow release and topiramate)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC202101498023

Write-up: top; head; Itching/itching and heat from my chest to the top of my head; This is a spontaneous report from a contactable consumer or other non-health care professional received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202110291237147720-ABUND, Safety Report Unique Identifier GB-MHRA-ADR 26139413. A 51-year-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number was not reported), via an unspecified route of administration on 02Feb2021 as DOSE 1, SINGLE for COVID-19 immunization. Medical history included Bariatric surgery (I take vitamins after bariatric surgery), Epilepsy (I have epilepsy in remission on Tegretol slow release and topiramate), DVT (deep vein thrombosis). The patient concomitant medications were not reported. Patient has not tested positive for COVID-19 since having the vaccine. Patient is not enrolled in clinical trial. Patient has not had symptoms associated with COVID-19. Patient is not pregnant, Patient is not currently breastfeeding. The patient previously took tegretol, topiramate, warfarin (after a DVT and PE). On an unspecified date, patient experienced top (abortion induced) and head. On 03Feb2021, patient experienced itching/ itching and heat from my chest to the top of my head. The events was reported as medically significant. Additional information: itching and heat from my chest to the top of my head. Initially I did not realize it was a reaction until I got the second dose when the reaction happened almost immediately. The reaction lasted several months. The patient underwent lab tests and procedures which included COVID-19 virus test was Negative (No - Negative COVID-19 test) on an unspecified date. Possible inflammation of the heart (myocarditis or pericarditis) was reported as no. The outcome of the event top and head was not recovered; the other event recovered on an unspecified date 2021. No follow-up attempts were possible; information about lot/batch number cannot be obtained. No further information was expected.; Sender''s Comments: Linked Report(s) : GB-PFIZER INC-202101506931 same patient/same product, different dose/events.


VAERS ID: 1016753 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: Connecticut  
Vaccinated:2021-01-28
Onset:2021-02-04
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-02-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenate DHA
Current Illness: None
Preexisting Conditions: None
Allergies: none
Diagnostic Lab Data: serum quantitative beta-hCG drawn on 2/4/21 (results not available).
CDC Split Type:

Write-up: 42yo G2P0010 at 3+6 weeks GA by LMP 1/1/2021 with EDD 10/8/2021 on day of Vaccine Dose #2 (1/28/2021), positive urine pregnancy test on 1/30/21. Bleeding began on 2/4/2021, and complete miscarriage occurred on 2/5-2/6.


VAERS ID: 1038516 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-01-21
Onset:2021-02-04
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-02-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

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

Life Threatening? No
Birth Defect? 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: US on 2/4, US on 2/16; serum beta HcG on 2/17
CDC Split Type:

Write-up: Patient received the vaccine on 1/21 she presented for her first OB US on 2/4 and pregnancy was found to be nonviable; Patient has D&C scheduled for next week and more information will be available at that time


VAERS ID: 1042347 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:2021-01-15
Onset:2021-02-04
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-02-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021130569

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer(patient). This is a maternal report. A female patient of an unspecified age (Age: 29; Unit: Unknown) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date were unknown), via an unspecified route of administration on 15Jan2021 at a single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient stated that her first dose of the Pfizer vaccine was on 15Jan2021 and reported that she had a miscarriage on Thursday 04Feb2021. It was reported that the patient missed her scheduled second dose of the Pfizer COVID-19 vaccine due to a miscarriage. The event was assessed as serious (medically significant). The outcome of the event was unknown. Information on the lot/batch number has been requested.


VAERS ID: 1078957 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Connecticut  
Vaccinated:2020-12-21
Onset:2021-02-04
   Days after vaccination:45
Submitted: 0000-00-00
Entered: 2021-03-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Unknown       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? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal
Current Illness:
Preexisting Conditions: Migraine
Allergies: Antibiotics
Diagnostic Lab Data: Ultrasound
CDC Split Type:

Write-up: Found out pregnant in between doses 1 (12/21)and (1/11). Lmp 12/13/2020. Was informed on 7 week ultrasound the fetal heart rate was low and Miscarriage likely. Miscarriage 2/4/2021.


VAERS ID: 1110984 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-01-19
Onset:2021-02-04
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-03-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3249 / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Cervical dilatation, Exposure during pregnancy, Haemorrhage, Premature delivery, Premature labour
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Normal pregnancy conditions and outcomes (narrow)

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

Write-up: a couple weeks after the vaccine I started bleeding Jan 3rd around 6pm that night, I relaxed at home later in the night I started having contractions at 4am I called my OB, I had an appointment the next morning and when I went in I was dilated 4cm so I went to deliver him that day. Everything was normal and baby was healthy. I was 36 weeks, original due date 3/4/2021, birth weight: 6lbs 2 z


VAERS ID: 1137811 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-04
Onset:2021-02-04
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-03-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9262 / 2 LA / SYR

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain upper, Abortion spontaneous, Feeling hot, Headache, Pain in extremity, Palpitations, Vaginal haemorrhage
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Mild reaction to 1st dose. Face was flushed with itchy spots.
Other Medications: Prenatal vitamins CoQ 10 - 500mg Vitamin C Ibuprofen and Benadryl - PRN
Current Illness: 1/14 - after the 1st shot my face was flush and had itchy spots, but went away w/o medical intervention
Preexisting Conditions: Hypothyroidism - after Dose 2
Allergies: Seasonal allergies/High pollen Kiwi - gives me a swollen tongue and itchy throat
Diagnostic Lab Data: Blood work - thyroid was abnormal. Was diagnosed with Hypothyroidism and my doctor doesn''t know if it''s related to the vaccine.
CDC Split Type: vsafe

Write-up: My first dose was 1/14. I found out I was pregnant on 1/26/21 and I miscarried at about 10 weeks. About 15 mins after I got the vaccine, I had a racing heartrate and my palms were hot, but it went away. Around 3pm, I had a right frontal headache. I took a nap and it went away. About 5am Fri, I woke up to severe arm pain and it felt like I was being stabbed in the stomach. I took about 400mg of Ibuprofen, went to sleep and was fine when I woke up. About 5pm Friday, I began having vaginal bleeding. I called my doctor and was able to get in on Feb 11th. At my OB/GYN appointment, they tested my blood and urine, which confirmed my pregnancy. The NP examined me and told me that the bleeding was coming from my cervix, so they sent me for an ultrasound the following week. That''s when I was given my calculated date of 10 weeks. A gestational sac was observed, but they weren''t sure if a fetus was present. I had to see my doctor every week since I was still bleeding and that continued until March 18th, when I lost the pregnancy completely. I took my specimen to the doctor the following day. They told me that they were sending it out to be tested, but I''m not sure if the results are back. They did confirm that it was a fetus.


VAERS ID: 1512867 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-01-05
Onset:2021-02-04
   Days after vaccination:30
Submitted: 0000-00-00
Entered: 2021-07-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011J20A / 1 - / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 013L200A / 2 - / IM

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

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

Write-up: Miscarriage on July 4th, approximately 6 weeks pregnant.


VAERS ID: 1035025 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-13
Onset:2021-02-04
   Days after vaccination:22
Submitted: 0000-00-00
Entered: 2021-02-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0203 / 1 LA / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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: CAPFIZER INC2021136705

Write-up: had a miscarriage at 8 week0 days of twins; This is a spontaneous report from a contactable physician report for self. This physician reported information for both mother (patient self) and two fetuses. This is a maternal report. A 34-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot EL0203) intramuscular at left arm on 13Jan2021 12:00 at single dose for covid-19 immunization. No allergies to medications, food, or other products. Patient was not diagnosed with covid-19 prior to vaccination. Patient not received any other vaccines within 4 weeks prior to the COVID vaccine. No other medications the patient received within 2 weeks of vaccination. Patient''s last menstrual period date was 10Dec2020. She was 4weeks5 days pregnant when received the 1st dose of the vaccine. She had a miscarriage at 8 week0 days on 04Feb2021 of twins but they were measuring 5weeks3 days. No treatment received for the adverse event. The event outcome was recovering. Since the vaccination, patient has not been tested for COVID-19.; Sender''s Comments: Based on available information, a possible contributory role of the subject product, BNT162B2 vaccine, cannot be excluded for the reported event of miscarriage due to temporal relationship. There is limited information provided in this report. Additional information is needed to better assess the case, including complete medical history, diagnostics, counteractive treatment measures and concomitant medications. This case will be reassessed once additional information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.


VAERS ID: 1579001 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-04
Onset:2021-02-04
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-08-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK9788 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion induced, Maternal 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? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: House dust mite allergy; Pollen allergy (Grass and tree pollen); Pregnancy
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC202100987996

Write-up: This is a spontaneous report from a non-contactable consumer or other non hcp downloaded from Agency. Sender''s safety report unique identifier DE-PEI-202100079387. This consumer or other non hcp reported information for both mother and fetus. This is the maternal report. A 38-year-old female patient received bnt162b2 (COMIRNATY), dose 2 via an unspecified route of administration on 04Feb2021 (Batch/Lot Number: EK9788) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included pregnancy, pollen allergy (Grass and tree pollen), house dust mite allergy, from an unknown date. The patient''s concomitant medications were not reported. Patient received her first dose of COMIRNATY on 31Dec2020 for COVID-19 immunisation. The patient''s weight was 50 kg, and height was 163 cm. On 23Feb2021, the patient experienced Pregnancy termination. On 09Mar2021 the patient experienced Fractional curettage. The affected person had to be treated as an inpatient. She had a poorly developed pregnancy in the 2nd-3rd month gestation (23Feb2021) with abrasion on 09Mar2021 in the 9th-10th week of pregnancy. The outcome of the events Pregnancy termination and Fractional curettage was Recovered/Resolved with Sequel.No follow-up attempts are possible. No further information is expected. Information about batch number has been obtained; Sender''s Comments: Linked Report(s) : DE-PFIZER INC-202101020613 fetus case


VAERS ID: 1028368 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: California  
Vaccinated:2021-01-27
Onset:2021-02-05
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-02-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9265 / 2 LA / IM

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

Life Threatening? No
Birth Defect? 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: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage in first trimester. First dose received 12/22/2020 Conception date 01/03/2021 Second dose 01/27/2021 Miscarriage started 02/03/2021 First pregnancy. No other medical problems or pregnancy risks.


VAERS ID: 1099293 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-01-28
Onset:2021-02-05
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-03-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / SYR

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

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

Write-up: I was between 4-5 weeks pregnant at the time of my 2nd Pfizer shot and miscarried 8 days after receiving the shot. I understand it is a possible coincidence however wanted to report seeing that I already carried a full healthy pregnancy to term in 2019.


VAERS ID: 1107944 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-01-22
Onset:2021-02-05
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-03-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA DOESN''T HAVE LO / 1 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Labetalol 200 mg
Current Illness: No
Preexisting Conditions: High blood pressure
Allergies: No
Diagnostic Lab Data: Sonogram, Bloodwork ABG level
CDC Split Type: vsafe

Write-up: After Dose1 I was 10 weeks pregnant went to doctor for sonogram. I went to doctor heart rate 160 doctor stated everything was fine I could start telling everyone I wa pregnant. On 2/5 I started having a miscarriage the fetus was 12 weeks. My blood work was good no abnormalities from the enzymes.(estimated of delivery 8/17/2021)


VAERS ID: 1378102 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Nevada  
Vaccinated:2021-02-05
Onset:2021-02-05
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9269 / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Gestational hypertension, Pre-eclampsia, Premature delivery
SMQs:, 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? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamins
Current Illness:
Preexisting Conditions:
Allergies: Penicillin
Diagnostic Lab Data:
CDC Split Type: vsafe

Write-up: After my vaccine, my baby had growth restriction, found out about this at 32 weeks. I developed gestational hypertension which turned into preeclampsia. My baby was born at 37 weeks. My baby is still small but is growing well. At the time of my second vaccine: I was 25 weeks


VAERS ID: 1174662 (history)  
Form: Version 2.0  
Age: 24.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-05
Onset:2021-02-05
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness: Pregnancy (Patient no longer pregnant at the time of reporting)
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid supplementation; Lactation decreased
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021319898

Write-up: miscarriage; maternal exposure during pregnancy; 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-202103221235348850. A 24-year-old female pregnant patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration on 05Feb2021 (batch/lot number and expiry date not reported) at the age of 24 years as single dose for covid-19 immunization. Medical history included lactation decreased, ongoing pregnancy (patient no longer pregnant at the time of reporting) and folic acid supplementation. The patient has not had symptoms associated with COVID-19, was not enrolled in clinical trial, was not currently breastfeeding. Concomitant medications included folic acid taken for vitamin supplementation from unspecified date. The patient experienced maternal exposure during pregnancy (05Feb2021) and miscarriage on 20Mar2021. The reporter informed that the mother reported she became pregnant while taking BNT162B2. The patient was exposed to the medicine first-trimester (1-12 weeks). The patient had a perfectly healthy pregnancy before and never had any issues, nobody in her family has ever had a miscarriage. The patient was extremely healthy, and exercise regularly so just wanted to be cautious that COVID may had an influence on this. The events were considered serious (disability, medically significant). The patient underwent lab tests and procedures which included COVID-19 virus test: no - negative COVID-19 test on unspecified date. The patient has not tested positive for COVID-19 since having the vaccine. The outcome of the event was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1225095 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-22
Onset:2021-02-05
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-04-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6789 / 1 LA / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnancy (Normal pregnancy and full term child in 2019)
Allergies:
Diagnostic Lab Data:
CDC Split Type: FRPFIZER INC2021363174

Write-up: Early miscarriage/pregnancy was terminated early at 5 1/2 weeks, accidentally and asymptomatically; This is a spontaneous report from a contactable physician downloaded from the regulatory authority-WEB FR-AFSSAPS-NT20210845. A 31-year-old female patient received the first dose of bnt162b2 (COMIRNATY), intramuscular, administered in left arm on 22Jan2021 (Batch/Lot Number: EJ6789) as single dose for covid-19 immunisation. Medical history included normal pregnancy and full term child in 2019 (G2P1 (two pregnancies, one birth)). The patient has no Covid-19 antecedent. The patient was not tested and has no usual treatment. The patient has no concomitant medications. The patient experienced early miscarriage on 05Feb2021. This was assessed as medically significant. The patient had exposure during pregnancy, first trimester. The patient received the first dose of the Comirnaty vaccine on 22Jan2021. An ultrasound was requested at 8 "WA" in principle by her gynecologist following the discovery of pregnancy after vaccination. The pregnancy was terminated early at 5 1/2 weeks, accidentally and asymptomatically. The vaccination was therefore carried out at 4 weeks. The patient presented no symptoms, including no bleeding. Vaccination was possible from a dose remaining at the end of the vaccination in the retirement home where she works. The outcome of the event was recovered on an unspecified date. No follow-up attempts are possible, information about lot number cannot be obtained. No further information is expected.


VAERS ID: 1025363 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-02-05
Onset:2021-02-06
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-02-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Foetal heart rate abnormal, Headache, Nausea, Pyrexia, Rash, Rash erythematous, Ultrasound uterus abnormal, Vomiting
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? 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: Folic acid 800mg
Current Illness: none
Preexisting Conditions: no
Allergies: no
Diagnostic Lab Data: Pregnancy was on 2/11, Second vaccine dose was on 2/5
CDC Split Type:

Write-up: About 12 hours after the vaccine I developed headache, fever 100.5, nausea and vomiting, and red rash across my chest up to my neck and under both breasts. All symptoms but the rash improved the following day. I went to have my 8 week pregnancy US 6 days after this second vaccine dose and there was no fetal heart rate. The baby measured 8.7mm and there should be a heart rate when the baby measures $g7mm. I had all of my pregnancy symptoms up through the day of the vaccine and then they disappeared the day my vaccine symptoms improved. I do not have a history of miscarriage.


VAERS ID: 1045927 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Nebraska  
Vaccinated:2021-02-04
Onset:2021-02-06
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 029L20A / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Back pain, Exposure during pregnancy, Human chorionic gonadotropin, Vaginal haemorrhage
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Omemprazole, Setraline, Claritin-D, Prenatal Vitamin
Current Illness: none
Preexisting Conditions: none
Allergies: dust, pet dander, seasonal
Diagnostic Lab Data: 2/8/2021: blood work to test hCG Quantitative levels. Levels were 29.54 mIU/mL showing positive pregnancy, but very low levels. Dr. suggested to repeat blood test in 2 days to see if levels were increasing or not to determine if miscarriage or possibly just very early pregnancy. 2/10/2021: repeat blood work to test hCG Quantitative levels. Level was 23.21 mIU/mL, slightly lower than previous level. Dr. confirmed this would mean early miscarriage, as a normal pregnancy they would expect that level to double each 24-48 hours. 02/18/2021: office visit as miscarriage symptoms had gotten worse on 2/17 w/ severe abdomen and back pain. Did repeat hCG Quantitative levels again which were 14.99, so still decreasing as expected. Ran blood work and urine tests to test for any anemia or infection, but all results were normal for that. Dr. confirmed symptoms still related to miscarriage and should improve soon.
CDC Split Type:

Write-up: positive at home pregnancy test 2/4/21 (same date as vaccine given). However, light bleeding/spotting started that night/next day but thought still normal. Heavier bleeding started 2/6/21 (Saturday) and continued through the weekend. Made appointment at hospital lab for Monday 2/8 to check HcG levels in blood. See below for details, but Dr. suggested repeat blood work on 2/10 as Hcg levels showed positive pregnancy, but very low. 2/10 Hcg levels slightly lower, which confirmed early miscarriage occurring.


VAERS ID: 1074467 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-01-28
Onset:2021-02-06
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-03-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Chills, Pelvic discomfort, Pregnancy, Ultrasound foetal abnormal
SMQs:, Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (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? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Micronized Progesterone supplements, prenatal vitamins, probiotics
Current Illness: No
Preexisting Conditions: Asthma
Allergies: Codeine
Diagnostic Lab Data: Normal ultrasound on Feb 5 (7 weeks 1 day gestation). Abnormal ultrasound on Mar 4 (7 weeks 2 days gestation).
CDC Split Type:

Write-up: Pregnancy loss: estimated due date was September 22, 2021. The only symptoms I experienced were pelvic cramping and chills. I did not have a fever. I received both doses during pregnancy. There is no explanation for the loss of the pregnancy. The baby showed as healthy and normal with a strong heartbeat on Feb 5 and the baby stopped growing and the heart stopped beating on Feb 6.


VAERS ID: 1127461 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-02-05
Onset:2021-02-06
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-03-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012M20A / 2 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Acute kidney injury, Blood pressure increased, Bradycardia, Caesarean section, Diarrhoea, Disseminated intravascular coagulation, Exposure during pregnancy, Fatigue, Foetal biophysical profile score abnormal, Foetal hypokinesia, Foetal monitoring, Foetal non-stress test abnormal, Hyponatraemia, Laboratory test abnormal, Malaise, Postpartum haemorrhage, Pre-eclampsia, Premature delivery, Uterine dilation and curettage, Vomiting
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (narrow), Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Pseudomembranous colitis (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hyponatraemia/SIADH (narrow), Hypertension (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Chronic kidney disease (broad), Noninfectious diarrhoea (narrow), Tumour lysis syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 10 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Keppra, levothyroxine, prenatals, folate, magnesium
Current Illness: none
Preexisting Conditions: seizure disorder, hypothyroid
Allergies: NKA
Diagnostic Lab Data: I would love to submit these in a document instead of typing it all out. There were too many labs and adverse results to type out here.
CDC Split Type:

Write-up: Date of 2nd vaccine I was 36+6 pregnant. Pregnancy was unremarkable to this date, an IVF pregnancy after infertility and one previous loss at 6 weeks. EDD 4/3/21. Day 1 after vaccine had 1 bout of vomiting, general fatigue/feeling unwell, diarrhea. Day 2 continued diarrhea. Day 3 continued diarrhea (12+ bouts/day), noted decreased fetal movements, went to midwife and had 8/8 BPP US and non-reactive NST. Sent home with recommendation to monitor fetal movements and hydrate. Day 4 had 3 bouts of vomiting, continued diarrhea 2/10/21 Day 5 after injection another bout of vomiting and continued diarrhea, went to clinic again and had non-reactive NST but was admitted for fluids, found to have hyponatremia and given IV saline. 8/8 BPP US, put on continuous fetal monitoring. No signs of labor. 2/11: elevated blood pressure, intermittent bradycardia, continued fetal monitoring, diarrhea improving, transferred to med-tele floor from L&D. labs though to r/o preeclampsia. 2/12: Diarrhea improving, continued tele and fetal monitoring, continued hyponatremia 2/13: fetal heart decels, repeated BPP at 2am and had score of 2/8. Urgent cesarean performed at 5:39 am. Apgars 5/8/8, 33 weeks gestation, 3#6 oz boy, admitted to NICU. I hemorrhaged after the cesarean and had D&C, later diagnosed with DIC and subsequently thought to have severe atypical preeclampsia. Hospital stay extended until 2/20/21 with high blood pressure, episodes of bradycardia, AKI.


VAERS ID: 1064725 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-15
Onset:2021-02-06
   Days after vaccination:22
Submitted: 0000-00-00
Entered: 2021-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0739 / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CITALOPRAM; FOLIC ACID; FOSTAIR
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Asthma; Depression; Eczema; Endometriosis
Allergies:
Diagnostic Lab Data: Test Date: 20210216; Test Name: COVID-19 virus test; Test Result: Negative
CDC Split Type: GBPFIZER INC2021177562

Write-up: Maternal exposure during pregnancy; Early miscarriage; This is a spontaneous report from a contactable consumer. This is a report received from the RA. Regulatory authority report number GB-MHRA-APPCOVID-20210216185033, Safety Report Unique Identifier GB-MHRA-ADR 24775752. A 21-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0739), via an unspecified route of administration on 15Jan2021 at single dose for COVID-19 immunisation. Medical history included endometriosis, asthma, eczema, depression. Patient has not had symptoms associated with COVID-19, is not enrolled in clinical trial. Patient was pregnant at time of vaccination. Concomitant medications included citalopram from 01Jan2020 to 16Feb2021 for depression; folic acid for folic acid supplementation; beclometasone dipropionate, formoterol fumarate (FOSTAIR) from 01Jan2021 for asthma. The patient experienced maternal exposure during pregnancy on an unspecified date with outcome of unknown, early miscarriage on 06Feb2021 with outcome of recovered on 12Feb2021. It was unsure patient was exposed to the medicine first-trimester (1-12 weeks). Patient tested negative for COVID-19 virus test on 16Feb2021. No follow-up attempts are possible. No further information expected.


VAERS ID: 1467713 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-20
Onset:2021-02-06
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-07-13
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, Incomplete course of vaccination, Pregnancy test
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210206; Test Name: Pregnancy test; Test Result: Positive
CDC Split Type: DEPFIZER INC2021129192

Write-up: unfortunately suffered a miscarriage a few weeks later; Because of the pregnancy, I had the appointment for that Second vaccination canceled.; Received the first dose of vaccine and had a positive pregnancy test; This is a spontaneous report based on information received by Pfizer from Biontech [manufacturer control number: 13560], license party for Comirnaty. As reported: Reporter type: Other HCP Product: BNT 162b2 Content of original e-mail: I received the first dose of your vaccine on 20Jan2021. On last week end, on 06Feb2021 I had a positive pregnancy test. Batch number not known Initial vaccination date: Jan 20, 2021 Booster date known? No Reporter is patient: Yes Patient gender: F Start date of reaction (comment): positive pregnancy test on 6Feb2021 Outcome information: Other Outcome information other: pregnancy Other important information available: No Initial administration / booster: Initial Health authority notified: Unknown Does enquiry involve a report of exposure during pregnancy? Yes Follow-up (PRD/SRD 20May2021), New information based on information received by Pfizer from Biontech manufacturer control number: 56256, license party for Comirnaty. from the consumer (patient) as reported: "Due to the pregnancy, I had canceled the appointment for the second vaccination, but unfortunately suffered a miscarriage a few weeks later." Outcome information: Unknown Lot/batch number has been requested.; Sender''s Comments: As there is limited information in the case provided, the causal association between the events abortion spontaneous, exposure during pregnancy and the suspect BNT 162b2 cannot be excluded. 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: 1040307 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-02-05
Onset:2021-02-07
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-02-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA UNKNOWN / 2 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Endometrin, progesterone in oil IM shots, Estrogen pills
Current Illness: none
Preexisting Conditions: none
Allergies: NKA
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Early miscarriage occurred on Sunday, 2/7/2021. No previous pregnancies


VAERS ID: 1041297 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-01-02
Onset:2021-02-07
   Days after vaccination:36
Submitted: 0000-00-00
Entered: 2021-02-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 026L20A / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Haemorrhage, Thrombosis, Vomiting
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Thrombophlebitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Termination of pregnancy and risk of abortion (narrow)

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

Write-up: I started bleeding on the 4th, doctor stated threaten miscarriage. I had blood clots and vomiting''. I was taking to emergency room. I was giving a DNC because I had a miscarriage.


VAERS ID: 1048833 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-01-22
Onset:2021-02-07
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-02-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL8982 / 2 LA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Gestational age test abnormal, Human chorionic gonadotropin, Human chorionic gonadotropin abnormal, Ultrasound scan vagina
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)

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: zyrtec, calcium w/ vitamin d, prenatal vitamns
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: ibuprofen, shrimp, strawberries
Diagnostic Lab Data: HCG & Transvaginal ultrasound 2/8 & 2/9
CDC Split Type:

Write-up: ~ 5 weeks pregnant at the time of 2nd vaccination. Miscarriage ~2 weeks later. Transvaginal ultrasound shows gestational age only 5 weeks when should have been 7. HCG level reflects only 4-5 weeks when should have been 7.


VAERS ID: 1060779 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Florida  
Vaccinated:2021-01-12
Onset:2021-02-07
   Days after vaccination:26
Submitted: 0000-00-00
Entered: 2021-02-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 039K20A / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Foetal death, Human chorionic gonadotropin positive, Ultrasound antenatal screen abnormal
SMQs:, 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)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Pre-natal vitamins Vyvanse 50mg Citalopram 40mg
Current Illness: None
Preexisting Conditions: None
Allergies: Amoxicillin
Diagnostic Lab Data: Feb. 10, 2021: Ultrasound (showing embryo of approx. 7 weeks with no heartbeat) Feb. 10, 2021: beta hCG levels. (approx. 17,000+) Feb. 12, 2021: Repeat of beta hCG levels. (approx. 7,000+, consistent with miscarriage) Feb. 19, 2021: Ultrasound (confirming loss of gestational sac and contents)
CDC Split Type:

Write-up: At 5 weeks, 5 days pregnant I received the 1st Covid-19 dose. I started bleeding the evening of Feb. 7, 2021. The bleeding continued to increase. I visited the Emergency Department on Feb. 10, 2021 and learned my baby had died around 7 weeks into the pregnancy.


VAERS ID: 1204891 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-06
Onset:2021-02-07
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-04-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / IM

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

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

Write-up: Miscarriage/spontaneous abortion


VAERS ID: 1242165 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-05
Onset:2021-02-07
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-04-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / IM

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

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

Write-up: Miscarriage at 4 weeks


VAERS ID: 1019778 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Missouri  
Vaccinated:2021-02-01
Onset:2021-02-08
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3302 / 1 RA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamin
Current Illness: none
Preexisting Conditions: childhood asthma
Allergies: none
Diagnostic Lab Data: Ultrasound 2/8/21
CDC Split Type:

Write-up: Miscarriage 1 week post getting dose 1 of vaccine. Estimated due date was 08/18/2021. Previous pregnancy history is 3 pregnancies, with 3 full term live births, no complications.


VAERS ID: 1032993 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-02-01
Onset:2021-02-08
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-02-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 028L20A / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Pregnancy, Retinal detachment, Visual impairment
SMQs:, Anticholinergic syndrome (broad), Accidents and injuries (broad), Glaucoma (broad), Optic nerve disorders (broad), Lens disorders (broad), Retinal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Pre-natal vitamin
Current Illness: No illness known. Involved in motor vehicle accident on 2/1/21, prior to being vaccinated- reports she sustained back pain and whiplash.
Preexisting Conditions: None known
Allergies: NKDA
Diagnostic Lab Data: HCG
CDC Split Type:

Write-up: Reports she was vaccinated on 2/1/21, found out she was pregnant on on 2/3/21, and miscarried the pregnancy on 2/8/21. Additionally, she was involved in a motor vehicle accident on 2/1/21, prior to her vaccine, sustaining back pain and whiplash. Lastly, reports she began having visual changes on 2/3/21 and was diagnosed with a detached retina on 2/10/21.


VAERS ID: 1050476 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Utah  
Vaccinated:2020-12-30
Onset:2021-02-08
   Days after vaccination:40
Submitted: 0000-00-00
Entered: 2021-02-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EH9899 / 1 - / IM

Administered by: Work       Purchased by: ?
Symptoms: Cytogenetic analysis normal, 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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Genetic testing of fetus was normal male, with no significant genetic issues
CDC Split Type:

Write-up: Fetal demise at gestational age 14 weeks. Exact age when patient received first dose of COVID-19 vaccine. Patient had suffered from hyperemesis prior to vaccine, but had improved prior to vaccine. No other complications in pregnancy estimated date of delivery was July 14, 2021


VAERS ID: 1056929 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Nebraska  
Vaccinated:2021-02-08
Onset:2021-02-08
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-02-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK4176 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Chills, Exposure during pregnancy, Lymphadenopathy, Myalgia, Nausea, Pyrexia, Tremor
SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

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

Write-up: That night my fever 102 took Tylenol to bring it down, shakes, chills , nausea, muscle aches and swollen lymph nodes (right armpit).The symptoms lasted to Sunday. My estimated date of delivery was Sept.14 I miscarried at 5 wks.


VAERS ID: 1059748 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Florida  
Vaccinated:2021-01-22
Onset:2021-02-08
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-02-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9263 / 1 LA / IM

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

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Pre-natal Vitamin, Tylenol, Rhinocort nasal spray
Current Illness:
Preexisting Conditions:
Allergies: KNA/KNDA
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: I went into preterm labor at 20 weeks, 3 days on and delivered a live pre-term baby boy who died shortly thereafter. He weighed 11 oz. My estimated delivery date was to be 06/25/2021. This was my second pregnancy, and I had not had my 20 week ultrasound yet. There is no known cause of why I experienced pre-term labor and an autopsy was not performed on my son. My first pregnancy was uneventful and I delivered at full-term.


VAERS ID: 1020661 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-02-03
Onset:2021-02-09
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-02-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN9581 / 1 RA / IM

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

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: Pertussis vaccine, late 1980s, apnea (but happened a few days after vaccine, so unsure if true allergy)
Other Medications: Pre natal vitamin
Current Illness: none
Preexisting Conditions: none
Allergies: Pertussis vaccine, Cefzil antibotic
Diagnostic Lab Data: Ultrasounds 2/4 and 2/9
CDC Split Type:

Write-up: I was 6 weeks pregnant when I got my first dose of the vaccine. I spoke with my OBGYN prior to the vaccine and she said it was safe t get. The day after the vaccine (2/4) I started having some vaginal bleeding, confirmed with ultrasound. This progressed to having a miscarriage, confirmed via ultrasound 2/9. My OBGYN said she does not think they are related, but there is no way to tell. Until 2/4, I had no issues with my pregnancy.


VAERS ID: 1033412 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-01-12
Onset:2021-02-09
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-02-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012L20A / 1 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Montelukast, loratidine, prenatal vitamin, magnesium supplement, 81mg aspirin
Current Illness: 20 weeks pregnant at time of vaccine 1/12/21; intrauterine fetal demise noted at regular OB visit 2/9/21
Preexisting Conditions: Asthma, migraines
Allergies: No known allergies
Diagnostic Lab Data: Fetal autopsy pending
CDC Split Type:

Write-up: 20 weeks gestation at time of vaccine administration. Saw OB that morning (1/12/21), normal exam and fetal heart rate. Normal anatomy scan 1/8/21, normal genetic screening. Fetal demise noted at 24 week OB visit on 2/9/21, stillborn baby delivered 2/12/21.


VAERS ID: 1038096 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-01-26
Onset:2021-02-09
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-02-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 027L20A / 1 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamin malarone daily for malaria prophylaxies
Current Illness: none
Preexisting Conditions: history of PCOS
Allergies: none
Diagnostic Lab Data: No testing performed.
CDC Split Type:

Write-up: Pt is G1P0. At the time she received the vaccine on 1/26/21 she was 13 weeks pregnant. She had normal 1st trimester ultrasound and normal prenatal labs. Her EDD is August 5, 2021. On 2/9/21 she had a spontaneous miscarriage. No subsequent complications. No history of drug or alcohol abuse. No s/sx of other causes of a early 2nd trimester miscarriage. Of note the 1st trimester genetic testing was unable to be performed due to low fetal free cell DNA when she was at 10w. We were in the process of repeating the labs when the miscarriage happened. No history of COVID infection, no s/sx of COVID infection at the time of the miscarriage or subsequently. She was not tested.


VAERS ID: 1143480 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-02-04
Onset:2021-02-09
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-03-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3249 / 2 RA / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: PRENATAL [FOLIC ACID;IRON]; FLUOXETINE
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021274265

Write-up: Miscarriage; spotting; This is a spontaneous report from a contactable nurse (patient). A 31-year-old female patient received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3249), intramuscular at right deltoid on 04Feb2021 at single dose for COVID-19 immunization. Medical history was reported as none. She has no known allergies and has no COVID prior to vaccination. Concomitant medications included folic acid, iron (PRENATAL) and fluoxetine. The patient has no other vaccine in four weeks. The patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: Ek9231) at the age of 31-years-old, intramuscular at right arm on 14Jan2021 at 12:30 at single dose for COVID-19 immunization. The vaccine was administered in a hospital. The patient was pregnant, her last menstrual period was on 19Dec2020. Her expected due date is on 25Sep2021 and gestational period was 7 weeks (also reported as 3). The patient experienced miscarriage and spotting on 09Feb2021 which resulted in doctor or other healthcare professional office/clinic visit. She was not tested for COVID post vaccination. The outcome of the events was recovering.; Sender''s Comments: Based on available information, a possible contributory role of the subject product, BNT162B2 vaccine, cannot be excluded for the reported events of miscarriage and vaginal hemorrhage due to temporal relationship. However, the reported events may possibly represent intercurrent medical conditions in this patient. There is limited information provided in this report. This case will be reassessed once additional information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.


VAERS ID: 1304102 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Florida  
Vaccinated:2021-01-04
Onset:2021-02-09
   Days after vaccination:36
Submitted: 0000-00-00
Entered: 2021-05-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 039K20A / 2 LA / -

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

Life Threatening? No
Birth Defect? 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: Wellbutrin and prenatal vitamins
Current Illness: N/a
Preexisting Conditions: N/a
Allergies: N/a
Diagnostic Lab Data: N/a
CDC Split Type:

Write-up: Initial dose 1/4/2021 second 1/29/2021. I was a little over 8 weeks pregnant when I had a miscarriage on or around 2/09. I was not aware that the baby did not have a heart beat at that time but learned at an ultrasound on 3/9. I had an d and c. The baby was due on 9/23/2021.


VAERS ID: 1388203 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-09
Onset:2021-02-09
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 016M20A / 2 LA / SYR

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain upper, Abortion spontaneous, Back pain, Blood test abnormal, Body temperature increased, Chills, Diarrhoea, Fatigue, Feeling abnormal, Headache, Heavy menstrual bleeding, Nausea, Pregnancy, Sleep disorder, Uterine dilation and curettage, Vomiting
SMQs:, Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Retroperitoneal fibrosis (broad), Dementia (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: multivitamin
Current Illness: none
Preexisting Conditions: none
Allergies: sulfa, Augmentin
Diagnostic Lab Data: blood test my blood levels were low in april
CDC Split Type: vsafe

Write-up: The same day right after the vaccination I felt weird but I left the mall after the 15 minute period and after I went home i vommitted and had back pains and just couldn''t sleep at all. At last I took Advil because I had chills. My temperature at that time was 103 I felt tired and for the next 36 hours my temperature was between 99-100 and I was in the bed the whole time I took Advil and Tylenol. I had an appointment with my doctor just to make sure everything is okay I couldn''t even go. I had diareeha for the longest time and then I had nausea and it went through for the longest time and I still have most of the symptoms my stomach hurts and I have headaches constantly. My blood tests are normal but i still can''t past the symptoms and my doctor says it can be related to the vaccination. On April 12 I had my periods but it was not that I just understand what that was it was really bad the blood was all over my body I went to the doctor and still nothing. I went to the emergency room for that and they gave me some medications to stop the blood but it didn''t help. my doctor did a dnd procedure because of the bleeding after the procedure I got the results and my tissue was of a pregnancy and I had a miscarriage and I didn''t even know.


VAERS ID: 1030540 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Rhode Island  
Vaccinated:2021-01-14
Onset:2021-02-10
   Days after vaccination:27
Submitted: 0000-00-00
Entered: 2021-02-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3246 / 2 LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal Vitamins, Docusate 100mg, Famotidine 20mg, 81mg Aspirin
Current Illness: Viral URI one month prior
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Still pending
CDC Split Type:

Write-up: Event - 22 week stillbirth Pregnancy history - G2P1001, EDD 6/13/2021, h/o twin gestation with 1st trimester vanishing twin. Otherwise uncomplicated.


VAERS ID: 1064425 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Vermont  
Vaccinated:2021-01-29
Onset:2021-02-10
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-03-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3246 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3249 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Headache, Physical examination, Ultrasound scan vagina, Uterine spasm, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

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

Write-up: I was about 9 weeks pregnant with no complications at the time of my second vaccination. Estimated due date was 08/24/2021. I began bleeding and cramping and having headaches approximately 10 days after my second dose. I sought medical attention and was told that my baby no longer had a heart beat and that growth (based on ultrasound) had stopped around the 9 week mark. I had medical assistance to physically miscarry the deceased fetus. I have one healthy living son (2 years, 4 months old) who was delivered without complications naturally.


VAERS ID: 1073098 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-01-11
Onset:2021-02-10
   Days after vaccination:30
Submitted: 0000-00-00
Entered: 2021-03-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / SYR

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? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: zyrtec, PNV
Current Illness: no
Preexisting Conditions: no
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: No adverse event occured, but I was 5 weeks pregnant at the time of the second vaccine and miscarried at 9 weeks.


VAERS ID: 1096757 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-02-02
Onset:2021-02-10
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-03-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / -
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 - / -

Administered by: Unknown       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, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: prenatal vitamin
Current Illness: none
Preexisting Conditions: morbid obesity with body mass index of 46
Allergies: Cefaclor
Diagnostic Lab Data: See description above. At this writing, the cause of fetal death is unknown. In this situation, we often never know the cause of death.
CDC Split Type:

Write-up: Patient received her Covid 19 vaccines on 1/6/21 and 2/3/21. On 3/3/21 at her routine prenatal visit, she was diagnosed with an intrauterine fetal demise. Based on the fetal measurements, the demise happened at 17-18 weeks of gestation, which would be sometime between 2/6/21 and 2/13/21. Medically, I don''t suspect that the demise is related to the vaccine, but for the sake of accurate tracking, I feel compelled to report the sequence of events.


VAERS ID: 1207875 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2020-12-19
Onset:2021-02-10
   Days after vaccination:53
Submitted: 0000-00-00
Entered: 2021-04-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy
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: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage. vaccinated December 19th. no Side effects. noticed a bit of pleuritic chest pain. was not bothersome and resolved with ibuprofen. I was pregnant at the time of first vaccine but did not know. had second vaccine 3 weeks after my first without issue. Went to OBGYn for 10 week appointment and there was no fetal pole. Fetus stopped developing at likely 6-7 weeks. I likely miscarried shortly after my second vaccine. .


VAERS ID: 1719154 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Alabama  
Vaccinated:2021-01-27
Onset:2021-02-10
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-09-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH R28982 / 2 RA / IM

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

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

Write-up: I took the 2nd vaccine in the series and I did not know that I was pregnant at the time. I started experiencing light bleeding and ultimately had a miscarriage 1.5-2 weeks after receiving the 2nd vaccine. My doctor did not think that the vaccine was attributed to the miscarriage. I have no previous history of miscarriage. Since this occurred within 30 days of receiving the vaccination, I believe that it should be reported. I am a healthcare worker and there has been zero communication/education or plea to the healthcare community to report adverse events for patients that receive the covid vaccines. As a researcher for phase 1 trials, we are required by the FDA to report all adverse events to the FDA whether the adverse event is attributed to study drug or not.


VAERS ID: 1114685 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-01
Onset:2021-02-10
   Days after vaccination:40
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Blood test, Chills, Nausea, SARS-CoV-2 test, Ultrasound scan
SMQs:, Acute pancreatitis (broad), 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:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Flu
Allergies:
Diagnostic Lab Data: Test Name: Blood tests; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210213; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:Negative; Test Name: ultrasound; Result Unstructured Data: Test Result:Unknown results
CDC Split Type: GBPFIZER INC2021228606

Write-up: nausea; chills; abdomen pains; Early miscarriage; This is a spontaneous report from a contactable Other HCP. This is a report received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202103011401524730, Safety Report Unique Identifier GB-MHRA-ADR 24857148. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration at single dose in Jan2021 for COVID-19 immunisation. Medical history included influenza (have the flu vaccine yearly at work). Patient had not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. Patient had not tested positive for COVID-19 since having the vaccine. Concomitant medication included influenza vaccine (INFLUENZA VIRUS) taken for immunization in Oct2020. The patient experienced nausea on an unspecified date with outcome of unknown, chills on an unspecified date with outcome of unknown, early miscarriage on 10Feb2021 with outcome of recovering, abdomen pains on an unspecified date with outcome of unknown. The patient underwent lab tests and procedures which included blood test: unknown results on unspecified date, SARS-CoV-2 test: negative on 13Feb2021, ultrasound scan: unknown results on unspecified date. The events were described as follows: Patient was 3-4 weeks pregnant unknowingly had the vaccine and then experienced chills, nausea and abdomen pains 2-3 weeks later diagnosed as a missed miscarriage and had to have medical management. Seriousness criteria of the events was reported as serious due to congenital anomaly and medically significant. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1316607 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-10
Onset:2021-02-10
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Intermenstrual bleeding, Maternal exposure timing unspecified, Pregnancy test
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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210215; Test Name: Pregnancy test; Test Result: Positive
CDC Split Type: FRPFIZER INC2021513200

Write-up: Miscarriage; Metrorrhagia; Maternal drug exposure; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority-WEB FR-AFSSAPS-NY20210792. A 29-year-old female patient received second dose bnt162b2 (COMIRNATY), intramuscular on 10Feb2021 (Batch/Lot Number: Unknown) at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously received first dose bnt162b2 (COMIRNATY), intramuscular on 20Jan2021 (Batch/Lot Number: Unknown) at single dose for COVID-19 immunisation. A 29-year-old female patient without specified medical history. Results of investigation at baseline: On 15Feb2021 pregnancy test was positive. The patient was exposed to COMIRNATY. On 05Apr2021, metrorragia and miscarriage, which were serious conditions from a medical standpoint. Conclusion was miscarriage with 9 SA metrorrhagia in a 29-year-old patient vaccinated with COMIRNATY (D1+D2). The mother was 9 Weeks pregnant at the onset of the events Metrorrhagia and Miscarriage. The outcome of the events Metrorrhagia and Miscarriage was recovered on 05Apr2021. No follow-up attempts are possible, information on batch number cannot be obtained.


VAERS ID: 1575639 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-09
Onset:2021-02-10
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-08-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK9788 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous complete, Herpes zoster, Malaise, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), 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: Adiposis (obesity); Smoker (nicotine abuse (20 py))
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnancy
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC202100988448

Write-up: Herpes zoster; Abortion spontaneous complete, 6 weeks pregnant; Pyrexia; feeling of illness; This is a spontaneous report from a non-contactable consumer(patient) downloaded from the regulatory authority-WEB, regulatory authority number DE-PEI-CADR2021057434. Sender''s (Case) Safety Report Unique Identifier DE-PEI-202100048679. A 36-year-old female patient received second dose of BNT162B2 (COMIRNATY)(strength 0.3 ml), via an unspecified route of administration on 09Feb2021, as single dose (Lot Number: EK9788) for covid-19 immunisation. The patient was pregnant at the time of vaccine. Medical history included smoker (reported as "nicotine abuse")( approx. 20 py) from an unknown date and was ongoing; adiposis(obesity) from an unknown date and was ongoing; pregnancy and was not ongoing. The patient''s concomitant medications were not reported. Allergies history was unknown. On 10Feb2021 the patient experienced pyrexia (reported as "fever") and feeling of illness only on the day after vaccination. On 11Feb2021 (the next day) the patient experienced abortion spontaneous complete (reported as "abortion") and the reporter did not suspect that this was related to the vaccination. Gestation period was 6 weeks when the abortion occurred. On 03Apr2021 the patient experienced herpes zoster (reported as "shingles"). Herpes zoster was treat with acyclovir by oral for 10 days. The outcome of fever and feeling of illness was recovered on 10Feb2021. The outcome of abortion spontaneous complete was recovered on an unspecified date in 2021. The outcome of herpes zoster was recovered in 19Apr2021. The relatedness of drug to reactions/events by regulatory authority was "D. Unclassifiable". This case was reported as serious due to medically significant condition. No follow-up attempts possible. No further information expected.; Sender''s Comments: The event of Abortion Spontaneous Complete is assessed as possibly related to the suspect drug BNT162B2 (COMIRNATY) based on temporal association 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: 1023866 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-01-15
Onset:2021-02-11
   Days after vaccination:27
Submitted: 0000-00-00
Entered: 2021-02-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3248 / 1 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Full blood count, Gynaecological examination abnormal, Human chorionic gonadotropin decreased, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? 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 vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: HCG and CBC blood work. 2/11. Vaginal exam by OBGYN 2/11
CDC Split Type:

Write-up: Miscarriage at 6 weeks 1 day. Vaginal bleeding and decline in HCG hormone. Pregnancy not viable.


VAERS ID: 1027542 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Rhode Island  
Vaccinated:2021-01-03
Onset:2021-02-11
   Days after vaccination:39
Submitted: 0000-00-00
Entered: 2021-02-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 026L20A / 1 LA / IM

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

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

Write-up: I conceived a pregnancy within 2 weeks of my vaccine which ultimately resulted in a miscarriage less than 6 weeks after the injection.


VAERS ID: 1042913 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2020-12-29
Onset:2021-02-11
   Days after vaccination:44
Submitted: 0000-00-00
Entered: 2021-02-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: N/a
Preexisting Conditions: N/a
Allergies: Penicillin- rash only
Diagnostic Lab Data: Ultrasound on 2/19/21 confirms loss of pregnancy
CDC Split Type:

Write-up: Could be completely unrelated but I had a miscarriage following COVID-19 vaccination.


VAERS ID: 1043944 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-07
Onset:2021-02-11
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-02-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness:
Preexisting Conditions:
Allergies: No allergies
Diagnostic Lab Data: Dropped hcg level not corresponding to gestational weeks 2/16/21
CDC Split Type:

Write-up: I was 5-week pregnant at the time of second COVID-19 vaccine dose. I had a gush of yellow vaginal discharge on 2/11 and subsequently spotting and bleeding up until pregnancy loss on 2/20.


VAERS ID: 1075313 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-02-11
Onset:2021-02-11
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-03-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3248 / 2 RA / OT

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Inappropriate schedule of product administration, Off label use, SARS-CoV-2 test
SMQs:, Termination of pregnancy and risk of abortion (narrow), Medication errors (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Allergies:
Diagnostic Lab Data: Test Date: 20210218; Test Name: Nasal Swab; Test Result: Negative
CDC Split Type: USPFIZER INC2021185868

Write-up: miscarried at 12 weeks; received first dose of bnt162b2 on 18Dec2020, second dose on 11Feb2021; received first dose of bnt162b2 on 18Dec2020, second dose on 11Feb2021; This is a spontaneous report from a contactable nurse (Patient). A 38-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number el3248) intramuscular in right arm on 11Feb2021 17:00 at single dose for covid-19 immunisation. No medical history. No COVID prior to vaccination. Other medications in two weeks include prenatal vitamins. Patient received first dose of bnt162b2 (lot number ek5730) on 18Dec2020 12:00 PM intramuscular in right arm. No other vaccine in four weeks. Patient''s last menstrual date was 01Nov2020. Patient miscarried at 12 weeks after receiving the second dose of vaccine. Dilation and curettage performed. Outcome was recovered with sequel. Nasal Swab COVID tested negative post vaccination on 18Feb2021.; Sender''s Comments: The limited information provided precludes a full clinical assessment of the case. Considering the product-event temporal relationship, a causal association between the reported ''miscarried'' and the administration of bnt162b2 cannot be completely excluded. Case will be reassessed once with additional information. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1096656 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-02-09
Onset:2021-02-11
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-03-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3244 / 1 RA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM9810 / 2 LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data: 3/4/21 ultrasound confirming growth stopped at 5 weeks. I was 5 weeks pregnant when I received the second dose. I have no health issues- nor dose my husband. I have never miscarried. I am 29, very healthy, and my first pregnancy was healthy all the way through.
CDC Split Type:

Write-up: I miscarried my baby two days after my second dose. I got pregnant between doses.


VAERS ID: 1271868 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Nevada  
Vaccinated:2021-02-04
Onset:2021-02-11
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-04-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Syncope, Uterine dilation and curettage, Vaginal haemorrhage
SMQs:, Torsade de pointes/QT prolongation (broad), Haemorrhage terms (excl laboratory terms) (narrow), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (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, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Asthma, migraines, eosinophilic esophagitis
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: I was 7 and half weeks pregnant when I received the second covid vaccine, then a week later, I began to have vaginal bleeding. 5 days after bleeding began, I miscarried while at home, passing a lot of tissue and lost a lot of blood, had to go the ER, had a syncopal episode due to blood loss and had to have an emergency D & C.


VAERS ID: 1028576 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Missouri  
Vaccinated:2021-02-11
Onset:2021-02-12
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-02-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0142 / 2 LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Zoloft 50mg, Zyrtec, PreNatal vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: Sulfa
Diagnostic Lab Data: 2/12/21 Blood type ABO+ RH Panel CBC W Auto differential Comprehensive metabolic panel HCG Beta Blood Quantitative - result 8.34
CDC Split Type:

Write-up: Was 5 weeks pregnant with 1st pregnancy due 10/12/21 and had a miscarriage the day after my 2nd dose. 2nd does was 2:30pm on Thursday. Had no side effects. 4:30pm the next day, Friday, began having miscarriage with no symptom warning.


VAERS ID: 1065703 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Kentucky  
Vaccinated:2021-01-26
Onset:2021-02-12
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 030L20A / 2 RA / IM

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

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

Write-up: Miscarriage at approximately 7 weeks pregnant


VAERS ID: 1090296 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Utah  
Vaccinated:2021-02-08
Onset:2021-02-12
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-03-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL3248 / 1 RA / IM

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

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

Write-up: Miscarriage


VAERS ID: 1116526 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2021-02-12
Onset:2021-02-12
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / SYR

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

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

Write-up: I experienced a missed miscarriage. I was pregnant during both doses of the vaccine (1st dose 1/15/21), but 2/12/21 (the day of the 2nd dose) was the day the gestational sac stopped growing. I was 8 weeks pregnant at this point. The ultrasound was on 2/17/21 and it was reported that I was supposed to be 8wk 6days, but gestational sac was only 8wk 1day. I was due on 9/23/21. My PCP encouraged me to get the vaccine, knowing that I was pregnant. So I did. Upon receiving my 2nd dose of the vaccine, I did not experience any symptoms and believe that my body was focused more on the vaccine than the development of the baby. Obviously I''m not positive that this was the cause, but I wanted to make it known, so I can hopefully prevent this from happening again, if the vaccine was indeed a contributor.


VAERS ID: 1099859 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-03
Onset:2021-02-12
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-03-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Urine analysis
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: Gravida I; Miscarriage; Parity 3; Suspected COVID-19 (Unsure when symptoms stopped)
Allergies:
Diagnostic Lab Data: Test Date: 20210209; Test Name: urine pregnancy test; Test Result: Positive
CDC Split Type: GBPFIZER INC2021215352

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer. This is a report received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202102251110564820, Safety Report Unique Identifier GB-MHRA-ADR 24833661. A 33-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiration date unknown), via an unspecified route of administration on 03Feb2021 at a single dose for COVID-19 immunization. Medical history included previous miscarriage on Dec2020, suspected COVID-19 from 03Apr2020 (unsure when symptoms stopped), and G1,P3. Not had a COVID-19 test. Patient is not enrolled in clinical trial. Concomitant medication included folic acid for folic acid supplementation. The patient experienced miscarriage which started on 12Feb2021. Seriousness criteria reported by the health authority was "congenital anomaly". The mother reported she became pregnant while taking BNT162B2. Patient was exposed to the vaccine during first trimester (1-12 weeks). It was unsure if the medicine had an adverse effect on any aspect of the pregnancy. The pregnancy resulted in spontaneous abortion. Patient has not tested positive for COVID-19 since having the vaccine. The patient underwent lab tests and procedures which included urine pregnancy test: positive on 09Feb2021. The event recovered on Feb2021. Patient was no longer pregnant at the time of reporting. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1038491 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-01-20
Onset:2021-02-13
   Days after vaccination:24
Submitted: 0000-00-00
Entered: 2021-02-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / SYR

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

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

Write-up: Patient was newly pregnant, received 2nd dose of covid vaccine. Patient then began bleeding on 2/13/21. On 2/15/21 confirmed with OBGYN that HCG levels were low and that she was having a miscarriage. Patient has a healthy 2 year old living child. No past history of miscarriages, no family history of miscarriage.


VAERS ID: 1069850 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Colorado  
Vaccinated:2021-01-20
Onset:2021-02-13
   Days after vaccination:24
Submitted: 0000-00-00
Entered: 2021-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, probiotic
Current Illness: None
Preexisting Conditions: Previous miscarriage x2; psoriasis
Allergies: none
Diagnostic Lab Data: Ultrasound, quant, D&C
CDC Split Type:

Write-up: LMP 1/10/2021. Moderna vaccine #2 1/20/2021. Positive pregnancy test 2/2/2021. Confirmed loss by US 2/13/2021 and decreasing quant. D&C 2/19/2021


VAERS ID: 1206919 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Connecticut  
Vaccinated:2021-01-19
Onset:2021-02-13
   Days after vaccination:25
Submitted: 0000-00-00
Entered: 2021-04-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 039K20A / 2 RA / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Pregnancy, Pregnancy test
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? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]; VITAMIN D [VITAMIN D NOS]; DHA; PROBIOTIC BLEND; LORATADINE; MAGNESIUM
Current Illness: Anxiety disorder; Drug allergy (sulfa, cephalosporins, codeine)
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnancy loss (first trimester loss)
Allergies:
Diagnostic Lab Data: Test Date: 20210226; Test Name: pregnancy test; Test Result: Positive ; Result Unstructured Data: positive
CDC Split Type: USMODERNATX, INC.MOD20210

Write-up: spontaneous miscarriage; conceived following second dose; This spontaneous case was reported by a pharmacist (subsequently medically confirmed) and describes the occurrence of ABORTION SPONTANEOUS (spontaneous miscarriage) in a 39-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 039K20A and 023M20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included Pregnancy loss (first trimester loss) on 01-Jun-2013 and Pregnancy loss (first trimester loss) on 23-Sep-2019. Concurrent medical conditions included Anxiety disorder, Drug allergy (sulfa), Drug allergy (cephalosporins) and Drug allergy (codeine). Concomitant products included MINERALS NOS, VITAMINS NOS (PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]), VITAMIN D [VITAMIN D NOS], DOCOSAHEXAENOIC ACID (DHA), BIFIDOBACTERIUM BIFIDUM, BIFIDOBACTERIUM LONGUM, LACTOBACILLUS ACIDOPHILUS, LACTOBACILLUS RHAMNOSUS (PROBIOTIC BLEND), LORATADINE and MAGNESIUM for an unknown indication. On 19-Jan-2021 at 11:20 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 18-Feb-2021 at 11:10 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 13-Feb-2021, the patient experienced PREGNANCY (conceived following second dose). On 06-Mar-2021, the patient experienced ABORTION SPONTANEOUS (spontaneous miscarriage) (seriousness criterion medically significant). On 06-Mar-2021, PREGNANCY (conceived following second dose) had resolved. At the time of the report, ABORTION SPONTANEOUS (spontaneous miscarriage) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 26-Feb-2021, Pregnancy test: positive (Positive) positive. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Date of last menstrual period was 29Jan2021 This spontaneous case was reported by a pharmacist (subsequently medically confirmed) and describes the occurrence of ABORTION SPONTANEOUS (spontaneous miscarriage) in a 39-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 039K20A and 023M20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included Pregnancy loss (first trimester loss) on 01-Jun-2013 and Pregnancy loss (first trimester loss) on 23-Sep-2019. Concurrent medical conditions included Anxiety disorder and Drug allergy (sulfa, cephalosporins, codeine). Concomitant products included MINERALS NOS, VITAMINS NOS (PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]), VITAMIN D [VITAMIN D NOS], DOCOSAHEXAENOIC ACID (DHA), BIFIDOBACTERIUM BIFIDUM, BIFIDOBACTERIUM LONGUM, LACTOBACILLUS ACIDOPHILUS, LACTOBACILLUS RHAMNOSUS (PROBIOTIC BLEND), LORATADINE and MAGNESIUM for an unknown indication. On 19-Jan-2021 at 11:20 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 18-Feb-2021 at 11:10 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 13-Feb-2021, the patient experienced PREGNANCY (conceived following second dose). On 06-Mar-2021, the patient experienced ABORTION SPONTANEOUS (spontaneous miscarriage) (seriousness criterion medically significant). On 06-Mar-2021, ABORTION SPONTANEOUS (spontaneous miscarriage) and PREGNANCY (conceived following second dose) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 26-Feb-2021, Pregnancy test: positive (Positive) positive. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Date of last menstrual period was 29 Jan 2021. This is a case of product exposure during pregnancy (5 weeks gestational age) with spontaneous abortion for this 39-year-old female. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded; Sender''s Comments: This is a case of product exposure during pregnancy (5 weeks gestational age) with spontaneous abortion for this 39-year-old female. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded


VAERS ID: 1099647 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-10
Onset:2021-02-13
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-03-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6789 / UNK LA / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Human chorionic gonadotropin, SARS-CoV-2 test negative
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: Coronavirus test negative; Deep vein thrombosis
Allergies:
Diagnostic Lab Data: Test Date: 2021; Test Name: beta-HCG; Result Unstructured Data: Test Result:234; Test Date: 20201021; Test Name: Covid-19 test; Test Result: Negative
CDC Split Type: FRPFIZER INC2021198623

Write-up: Miscarriage; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority-WEB and received via Regulatory Authority FR-AFSSAPS-NT20210344. A 36-year-old female patient received bnt162b2 (COMIRNATY, solution for injection, lot number: EJ6789, expiry date was not reported), intramuscular in the left arm on 10Feb2021 at a single dose for COVID-19 immunisation. Medical history included coronavirus test negative and deep vein thrombosis in 2016. Concomitant medication included folic acid. The patient was pregnant when the vaccine was given. She had no history of Covid-19. The patient experienced miscarriage on 13Feb2021 with outcome of recovered with sequelae on 13Feb2021. It was reported that the occurrence of the event was in the first trimester of pregnancy. The patient received a dose of COMIRNATY vaccine against COVID-19 on 10Feb2021. Three days later, she presented with metrorrhagia revealing an arrested pregnancy. Evolution: recovered/resolved with sequelae. On 19Feb2021 update, it was mentioned that the patient had very early pregnancy, 13Jan2021 i.e. 4 weeks of amenorrhea on the day of the vaccine, beta-HCG at 234 the next day (in 2021). Pfizer D2 vaccine. The mother reported she became pregnant while taking bnt162b2. The mother was 4 Weeks pregnant at the onset of the event. The mother was due to deliver on 20Oct2021.The pregnancy resulted in spontaneous abortion. The fetal outcome is neonatal death. The patient underwent lab tests and procedures which included Covid-19 test with negative result on 21Oct2020. NB: Accountability without prejudice to the elements of investigation which could be carried out within the framework of legal procedures. No follow-up attempts are possible. No further information expected. Lot/batch number was provided.


VAERS ID: 1297436 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-14
Onset:2021-02-13
   Days after vaccination:30
Submitted: 0000-00-00
Entered: 2021-05-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK1768 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Heart rate decreased, Maternal exposure during pregnancy, SARS-CoV-2 test, Ultrasound scan
SMQs:, Arrhythmia related investigations, signs and symptoms (broad), 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; Miscarriage; Pregnancy (Patient no longer pregnant at the time of reporting.); Pregnancy; Suspected COVID-19
Allergies:
Diagnostic Lab Data: Test Date: 20210414; Test Name: CRL - slow heart beat (feutus); Result Unstructured Data: Test Result:CRL 2.8 slow heart beat; Test Date: 20201123; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:Yes - Positive COVID-19 test; Test Date: 20210206; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:1st miscarriage; Test Date: 20210414; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:2nd miscarriage; Test Date: 20210420; Test Name: Ultrasound scan; Result Unstructured Data: Test Result:confirms miscarriage; Comments: subsequent scan
CDC Split Type: GBPFIZER INC2021449775

Write-up: Maternal exposure during pregnancy; Miscarriage; This is a spontaneous report from the Regulatory Authority, report number is GB-MHRA-WEBCOVID-202104211048235150-V1USE; Safety Report Unique Identifier: GB-MHRA-ADR 25173636. A contactable physician reported that a 41-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 14Jan2021 (lot number: EK1768; expiry date: unknown) at a single dose, for COVID-19 immunisation. Medical history included lactation decreased, miscarriage, pregnancy, pregnancy (patient no longer pregnant at the time of reporting), and suspected COVID -19 from 21Nov2020 to 07Dec2020. Patient is not enrolled in clinical trial. Patient is not currently breastfeeding. Concomitant medication included folic acid taken for folic acid supplementation. The patient experienced maternal exposure during pregnancy on an unspecified date and miscarriage on 13Feb2021. The events were considered serious due to other medically important condition. Clinical course: Patient received Pfizer vaccine on 14Jan2021. Patient conceived on 23Jan2021. Then subsequently had a miscarriage on 13Feb2021. Subsequent ovulation and conception on 27Feb2021 without a period in between and a second miscarriage confirmed 14Apr2021. There were two miscarriages back to back following the vaccine. Patient stated that she previously had two normal uncomplicated pregnancies. The report that the medicine has an adverse effect on any aspect of the pregnancy stated "Yes". Pregnancy adverse effects details: Two miscarriages since the vaccine. Details of previous pregnancies: 2 previous pregnancies: uncomplicated. Patient was exposed to the medicine before pregnancy. Details of scans or investigations: 1st miscarriage on 06Feb2021; 2nd miscarriage 14Apr2021 - CRL 2.8 slow heartbeat and likely miscarriage; subsequent scan on 20Apr2021 confirms miscarriage. The patient underwent lab tests and procedures which included COVID-19 virus test: yes - positive on 23Nov2020. Outcome of the event miscarriage was not recovered. Patient has not tested positive for COVID-19 since having the vaccine. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1751014 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-10
Onset:2021-02-13
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-10-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL7834 / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC202101226589

Write-up: Miscarriage; This is a spontaneous report from a contactable physician. This is a report received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202109171342464050-D9HZO, Safety Report Unique Identifier GB-MHRA-ADR 25959145. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; batch/lot number: EL7834; expiration date not provided) via an unspecified route of administration on 10Feb2021 (also reported as 10Mar2021) as DOSE 1, SINGLE for COVID-19 immunisation. Patient''s medical history and concomitant medications were not reported. It was reported that No current significant medical conditions. Patient has not had symptoms associated with COVID-19. Patient has not had a COVID-19 test. Patient is not enrolled in clinical trial. The patient experienced miscarriage on 13Feb2021 (also reported as 13Mar2021). Patient''s clinical course is as follows: It was reported that patient received first dose of Pfizer vaccine on 10Mar2021, on 13Mar2021, patient had a miscarriage, she was 6-8 weeks pregnant at the time. It was unknown if the vaccination caused the miscarriage or whether it was coincident but wanted to report it. The event was assessed as serious (medically significant). The patient has not tested positive for COVID-19 since having the vaccine. The report does not relate to possible blood clots or low platelet counts. At the time of reporting, outcome of the event was reported as recovered on 03Mar2021. No follow-up attempts are needed. No further information is expected.


VAERS ID: 1047157 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-01-25
Onset:2021-02-14
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 - / IM

Administered by: Senior Living       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Human chorionic gonadotropin decreased, Migraine
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Fertility disorders (narrow)

Life Threatening? No
Birth Defect? 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 with omega 3; vitamin d3
Current Illness: N/a
Preexisting Conditions: Digestive issues related to previous gastritis/stress
Allergies: N/a
Diagnostic Lab Data: Miscarriage completed naturally without medical intervention. Cause unknown.
CDC Split Type:

Write-up: Miscarriage at 8 weeks of pregnancy, 2/14/21. Tissue passed naturally without medical intervention. Hormone levels dropped without concern. The week prior to miscarriage sharp sporadic headaches (migraine-like but only lasting a few minutes at a time and coming frequently) started, and have continued daily through today (2/22/21)


VAERS ID: 1149346 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: California  
Vaccinated:2021-02-11
Onset:2021-02-14
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-03-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 016M20A / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Cerebral haemorrhage foetal, Exposure during pregnancy, Foetal death
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

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

Write-up: Patient was 30 weeks pregnancy with an uncomplicated pregnancy. She was found to have a fetal demise 3 days after her 2nd Covid19 vaccine. Vaccine 2/11/21, fetal demise 2/14/21. The fetus appears to have had an intracranial hemorrhage; work-up for this by parental testing is ongoing.


VAERS ID: 1064867 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-02
Onset:2021-02-14
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-03-02
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: Comments: Patient has not had symptoms associated with COVID-19 Not had a COVID-19 test Patient is not enrolled in clinical trial
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021170242

Write-up: Miscarriage; This is a spontaneous report from a contactable healthcare professional. This is a report received from the RA. Regulatory authority report number GB-MHRA-WEBCOVID-202102160821180080, Safety Report Unique Identifier GB-MHRA-ADR 24770068. A 21-year-old female patient received the first dose of BNT162B2, via an unspecified route of administration on 02Feb2021 at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient experienced miscarriage on 14Feb2021. Patient had not tested positive for COVID-19 since having the vaccine. The vaccine had an adverse effect on pregnancy-miscarriage. Patient was exposed to the medicine first-trimester (1-12 weeks). Patient had not had symptoms associated with COVID-19 and not had a COVID-19 test. Patient was not enrolled in clinical trial. Outcome of the event was resolving. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1109863 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-01
Onset:2021-02-14
   Days after vaccination:13
Submitted: 0000-00-00
Entered: 2021-03-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6795 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Chills, Headache, Myalgia
SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: DESLORATADINE
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLPFIZER INC2021226267

Write-up: Miscarriage; Headache; Cold shivers; Muscle pain; This is a spontaneous report from a contactable consumer. This is a report received from the Regulatory Authority. Regulatory authority or other manufacturer number NL-LRB-00445222. A 26-year-old female patient received the second dose of bnt162b2 (COMIRNATY) lot number: EJ6795, via an unspecified route of administration on 01Feb2021 as single dose for COVID-19 immunisation. Medical history was reported. Concomitant medication included desloratadine. On 14Feb2021, the patient had a miscarriage at 6 weeks of pregnancy. The patient stated that just after the 2nd vaccination came, she found out that she was pregnant. The miscarriage occurred at gestational age 6 weeks, 13 days after the second covid-19 vaccination. The patient also experienced headache, chills and myalgia on an unspecified date. The patient was recovering from the event miscarriage. The outcome of other events was recovered on an unspecified date. No follow-up attempts possible. No further information expected.


VAERS ID: 1630756 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-14
Onset:2021-02-14
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-08-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLPFIZER INC202101017609

Write-up: Missed miscarriage discovered on 03-08. At 8 weeks the heart stopped beating while I was 12 weeks pregnant. The exorcism has yet to take place.; Vaccination 3 months before pregnancy; This is a spontaneous report from a contactable consumer or other non hcp downloaded from the regulatory authority, regulatory authority number NL-LRB-00651922. This consumer reported information for both mother and fetus/baby. This is the maternal report. A 32-year-old pregnant female patient received bnt162b2 (COMIRNATY), dose 2 at the age of 32-years-old via an unspecified route of administration on 14Feb2021 (Batch/Lot Number: Unknown), prior to pregnancy/conception as DOSE 2, SINGLE for covid-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient received the first dose of bnt162b2 (COMIRNATY) on 24Jan2021 for covid-19 immunisation. The patient had her vaccination 3 months before pregnancy/conception on 14Feb2021. On 03Aug2021, the patient found out that she had a missed miscarriage. At 8 weeks the heart stopped beating while she was 12 weeks pregnant. The exorcism has yet to take place. Between 8 and 12 weeks. The fetal outcome was intrauterine death. The outcome of the events was unknown. No follow-up attempts are possible, information on batch number cannot be obtained.; Sender''s Comments: Linked Report(s) : NL-PFIZER INC-202101060370 baby case


VAERS ID: 1033516 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-01-29
Onset:2021-02-15
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-02-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 010M20A / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Headache, Pain in extremity, Sleep disorder, Ultrasound abdomen abnormal, Ultrasound scan vagina abnormal
SMQs:, Retroperitoneal fibrosis (broad), 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), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal multivitamin, iron supplement
Current Illness: On 1/20/2021 tested for Covid-19 via nasal swab due to having sore throat, fatigue, and headache. Test results came back negative that same day.
Preexisting Conditions: No chronic health issues, otherwise very healthy.
Allergies: NKA
Diagnostic Lab Data: On 2/16/21 I had an abdominal and vaginal ultrasounds, which confirmed absence of fetus in the uterus. Eptopic pregnancy was ruled out. MD was consulted on the same day regarding miscarriage.
CDC Split Type:

Write-up: At the time of administration of the first does of Moderna vaccine, I was 6 weeks pregnant. I had confirmed pregnancy with home positive test and missed period. I had an estimated due date of 9/24/2021. This was my 4th pregnancy. I have had two uncomplicated pregnancies to term. In September 2020 experienced a chemical pregnancy with early pregnancy loss at 5 weeks. The first 24 hours after 1st dose of vaccine I experienced extreme arm soreness in the arm that was vaccinated, causing headache and unable to sleep. After 24 hours I felt "normal". 2 weeks and 3 days following the first dose of Moderna, I had a miscarriage. On the night of 2/15/21 I lost the pregnancy with vaginal bleeding, bright red blood, passing tissue, clots/ sac. I had an uneventful pregnancy up to that point, feeling well as I had with prior pregnancies.


VAERS ID: 1051502 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-02-12
Onset:2021-02-15
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-02-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6201 / 2 LA / IM

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

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: HCG 27693 on 2/16/21 HCG 9321 on 2/18/21
CDC Split Type:

Write-up: Approx 6 weeks at time of second administration with a due date of sept 28th. Would have been 3 weeks pregnant at time of 1st injection. 3 days after second injection, I began to miscarry. This was confirmed by declining HCG levels. Ultrasound to follow in one week.


VAERS ID: 1053973 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2020-12-16
Onset:2021-02-15
   Days after vaccination:61
Submitted: 0000-00-00
Entered: 2021-02-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 UN / IM

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

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: OBGYN D&C removal at same day surgery center
CDC Split Type:

Write-up: Wife did not know she was pregnant at the time, had the vaccine and miscarried the child at 12 weeks. OBGYN stated baby had miscarried 2-3 weeks earlier. D&C procedure performed 2/23 to remove remains of fetus.


VAERS ID: 1060131 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-01-28
Onset:2021-02-15
   Days after vaccination:18
Submitted: 0000-00-00
Entered: 2021-02-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 025L20A / 1 RA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 043L20A / 2 RA / IM

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

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

Write-up: 1st vaccine: December 31 2020 2nd vaccine: January 28, 2021 Positive pregnancy test January 29 (2 positive tests on January 29, and 2 positive pregnancy tests on January 30) Estimated Due date October 8, 2021 Miscarriage on February 15, 2021


VAERS ID: 1073958 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-01-31
Onset:2021-02-15
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-03-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 010M20A / 1 LA / SYR
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012A21A / 2 LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Progesterone in oil, estradiol patches, baby aspirin, prenatal vitamin, vitamin D
Current Illness: None
Preexisting Conditions: Nine
Allergies: None
Diagnostic Lab Data: Ultrasound on February 15th HCG levels February 15th Ultrasound on February 18th HCG levels February 18th HCG levels February 25th
CDC Split Type:

Write-up: This was an IVF pregnancy. My 2nd pregnancy. I got my first positive pregnancy test on Jan. 27th at exactly 4 weeks pregnant. I received my first vaccine at 4 weeks 4 days. I then went in for my first ultrasound at 6 weeks 5 days. The doctor told me the baby wasn?t developed normally and a miscarriage had already started. I believe the gestational sac measured about 5 weeks 3 days.


VAERS ID: 1219039 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-02-14
Onset:2021-02-15
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-04-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 006M20A / 2 RA / IM
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 028L20A / 1 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Asthenia, Chills, Exposure during pregnancy, Fatigue, Full blood count, Headache, Human chorionic gonadotropin negative, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? 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 daily
Current Illness: Miscarriage noted on 3/25/21. Due date was supposed to be 11/14/21. Last me trial period was 2/7/21.
Preexisting Conditions: N/a
Allergies: N/a
Diagnostic Lab Data: Beta HCG until negative after miscarriage as well as CBC.
CDC Split Type:

Write-up: After 2nd shot I had a fever ($g101), headache, chills, fatigue & weakness. This went on for about 24 hours. I also had a miscarriage, diagnosed on 3/25/21. My due date was supposed to be 11/14/21.


VAERS ID: 1670822 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Ohio  
Vaccinated:2021-01-27
Onset:2021-02-15
   Days after vaccination:19
Submitted: 0000-00-00
Entered: 2021-09-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 094N020A / 2 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Discharge, 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? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zinc; vitamin D
Current Illness:
Preexisting Conditions:
Allergies: Codeine
Diagnostic Lab Data: DNC
CDC Split Type: vsafe

Write-up: I must have been pregnant at the time of vaccine but I did not know, my baby did not live, they had to do a DNC. So it all started when I skipped my period. I took a pregnancy test on 02-15-2021 and it was positive. On 02-17-2021 I had some discharge with calcifications and so I went to see my doctor and she could not find a heart beat. They did a DNC on 02-25-2021. My baby would have been 6 weeks when I had the DNC.


VAERS ID: 1512314 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-31
Onset:2021-02-15
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-07-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK9788 / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: DYMISTA
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Headache
Allergies:
Diagnostic Lab Data:
CDC Split Type: DKPFIZER INC2021890480

Write-up: Spontaneous abortion week 6. Unknown pregnancy when vaccinated.; This is a spontaneous report downloaded from the Regulatory Authority-WEB EudraVigilance-WEB received from a psysician from the Patient Compensation Association via the Regulatory Authority. This physician reported information for both mother and fetus. This is a maternal report. A 34-year-old female patient received second dose of BNT162B2 (COMIRNATY) via an unspecified route of administration on 31Jan2021 (Batch/Lot Number: EK9788; Expiration Date: 31May2021) as dose 2, single for covid-19 immunization. The patient''s medical history includes headache. Concomitant medication included azelastine hydrochloride, fluticasone propionate (DYMISTA) taken for headache from 16Jul2020 to an unspecified stop date. The patient received first dose of Comirnaty on 07Jan2021 (1st dose, lot/batch no.: EM0477; 1 DF). On 15Feb2021, the patient experienced spontaneous abortion week 6. unknown pregnancy when vaccinated. The mother reported she became pregnant while taking BNT162B2. The mother was 6 Weeks pregnant at the onset of the event. The pregnancy resulted in spontaneous abortion. No test results reported. Outcome of the event was not recovered. No follow-up attempts are possible. No further information expected.; Sender''s Comments: Linked Report(s) : DK-PFIZER INC-202100939581 reporter/patient/drug, different dose/events


VAERS ID: 1039396 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-02-14
Onset:2021-02-16
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-02-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Levothyroxine, calcium, calcitriol, folic acid
Current Illness:
Preexisting Conditions: Thyroid cancer s/p total thyroidectomy c/b hypoparathyroidism
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Miscarriage: vaginal bleeding with clots and tissue within 1 week of a positive home pregnancy test, two days after vaccination. Blood HCG take once vaginal bleeding commenced was <5.


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