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From the 11/12/2021 release of VAERS data:

Found 2,620 cases where Vaccine is COVID19 and Symptom is Aborted pregnancy or Abortion or Abortion complete or Abortion early or Abortion incomplete or Abortion induced or Abortion late or Abortion missed or Abortion of ectopic pregnancy or Abortion spontaneous or Abortion spontaneous complete or Abortion spontaneous incomplete or Foetal cardiac arrest or Foetal death or Premature baby death or Premature delivery or Stillbirth

Government Disclaimer on use of this data



Case Details (Sorted by Onset Date)

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VAERS ID: 1746193 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-02-05
Onset:2021-09-23
   Days after vaccination:230
Submitted: 0000-00-00
Entered: 2021-09-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Positive pregnancy test 8/22/21. HCG levels 9/29/21 and 10/1/21
CDC Split Type:

Write-up: Miscarriage. Two previous pregnancies with no complications.


VAERS ID: 1780470 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: California  
Vaccinated:2021-09-10
Onset:2021-09-23
   Days after vaccination:13
Submitted: 0000-00-00
Entered: 2021-10-13
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH PFIZER FD8448 / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Chills, Exposure during pregnancy, Infection, Injection site haemorrhage, Oropharyngeal pain, Pyrexia, Rash, Urine analysis, Vomiting
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: blood samples were taken and urine sample was given antibitiocs and was told this was probably not relcated to vacinne it did not hapen until after i gotn vacinated
CDC Split Type:

Write-up: At the time of vaccination i was approximately 3-4weeks pregnant according to my last menstrual cycle test''s showed positive 3 were taken and primary doctor appt was set. Started having fever,chills,throwing up and real bad rash around my belly button and on both inner arms inside elbow. Went to emergency room and informed nurses i just got vaccinated and this is happening and chose to ignore my symptoms. I informed doctor''s i was pregnant was advise i was no longer pregnant miscarriage. i did get an infection and throat was sore. I did bleed at the time of my shot once injected i was bleeding alot on my left arm. I keep having symptoms


VAERS ID: 1778720 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-10
Onset:2021-09-23
   Days after vaccination:13
Submitted: 0000-00-00
Entered: 2021-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FD7206 / 1 RA / -

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? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: MULTIVITAMIN N [AMINOBENZOIC ACID;ASCORBIC ACID;BETAINE HYDROCHLORIDE;BIOFLAVONOIDS NOS;BIOTIN;CALCI
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Normal pregnancy
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAPFIZER INC202101281587

Write-up: I miscarried 13 days later; This is a spontaneous case received from a contactable consumer (patient). This consumer reported information for both mother and fetus. This is the maternal report. A 32-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Right on 10Sep2021 13:45 (Lot Number: FD7206) as single dose (at the age of 32-years-old) for COVID-19 immunization in Hospital. Medical history included 4 healthy, successful pregnancies. Not diagnosed with COVID prior vaccination. Concomitant medication included aminobenzoic acid, ascorbic acid, betaine hydrochloride, bioflavonoids nos, biotin, calcium, calcium pantothenate, choline bitartrate, colecalciferol, copper, cyanocobalamin, folic acid, glutamic acid, hesperidin, inositol, iodine, iron, magnesium, manganese, nicotinamide, potassium, pyridoxine hydrochloride, retinol palmitate, riboflavin, rutoside, thiamine mononitrate, tocopheryl acetate, zinc (MULTIVITAMIN N [AMINOBENZOIC ACID;ASCORBIC ACID;BETAINE HYDROCHLORIDE;BIOFLAVONOIDS NOS;BIOTIN;CALCIUM;CALCIUM PANTOTHENATE;CHOLINE BITARTRATE;COLECALCIFEROL;COPPER;CYANOCOBALAMIN;FOLIC ACID;GLUTAMIC ACID;HESPERIDIN;INOSITOL;IODINE;IRON;MAGNESIUM;MAN). No other vaccine in four weeks. The patient reported, "I miscarried 13 days later" on 23Sep2021 12:00. Event resulted in Doctor or other healthcare professional office/clinic visit, Congenital anomaly or birth defect (as reported). The mother reported she became pregnant while taking bnt162b2. The mother was 7 Weeks pregnant at the onset of the event. The mother was due to deliver on 13May2022. The pregnancy resulted in spontaneous abortion. Reported as: "At the time of my injection I was 5 weeks pregnant. I miscarried 13 days later. I have no history of pregnancy complications, bleeding, spotting, and no history of miscarriage. I have had 4 healthy, successful pregnancies. I have no reason to believe this pregnancy would have been any different if not for receiving this vaccine which doesn''t have adequate testing on pregnant women." No treatment received. The outcome of the event was recovered with sequelae. Not tested for COVID post vaccination.


VAERS ID: 1786889 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-07-04
Onset:2021-09-23
   Days after vaccination:81
Submitted: 0000-00-00
Entered: 2021-10-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure before 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? 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
Allergies:
Diagnostic Lab Data: Test Name: SARS-CoV-2 test; Test Result: Positive ; Comments: corona, confirmed with test
CDC Split Type: NLPFIZER INC202101331240

Write-up: Vaccination 4 weeks before pregnancy; Miscarriage week 8; This is a spontaneous report from a contactable consumer or other non-healthcare professional downloaded from the regulatory agency-WEB NL-LRB-00689614. This serious spontaneous report from a consumer or other non-health professional concerns a female aged 33 years. A 33-years-old female patient (not pregnant at the time of vaccination) received first dose of bnt162b2 (COMIRNATY, solution for injection, Lot Number: not reported, Expiry date: unknown) via an unspecified route of administration, on 04Jul2021 as dose 1, single for COVID-19 immunization. Medical history included covid-19 (COVID-19 infection: disease symptoms: little) from an unknown date and unknown if ongoing. The patient''s concomitant medications were not reported. On 23Sep2021, the patient experienced miscarriage week 8. Vaccination 4 weeks before pregnancy. The miscarriage occurred at a pregnancy duration of about 8 weeks. This was the first covid vaccination, which took place before pregnancy. Miscarriage occured 3 months after start. On an unspecified date, the patient underwent lab tests and procedures which included sars-cov-2 test: positive on corona, confirmed with test. The outcome of the events was unknown. sender''s comments Since the nature of the reported reaction does imply seriousness according to one of the CIOMS criteria, the reaction was considered as serious by the regulatory agency. Reporter comment: BioNTech/Pfizer vaccine (Comirnaty), Past drug therapy BioNTech/Pfizer vaccine (Comirnaty): no, Miscarriage, Additional information ADR: Miscarriage with conception within 2 months after the vaccination. Miscarriage at 8 weeks. confounding factors: vaccine exposure during pregnancy week: -4; COVID19 : Previous COVID-19 infection: disease symptoms: little The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up.


VAERS ID: 1806466 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-08-26
Onset:2021-09-23
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3004234 / 1 LA / OT

Administered by: Unknown       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: FRMODERNATX, INC.MOD20213

Write-up: Miscarriage; Maternal Exposure During Pregnancy; This case was received via Regulatory Authority(Reference number: FR-AFSSAPS-NT20214396) on 11-Oct-2021 and was forwarded to Moderna on 11-Oct-2021. This regulatory authority retrospective pregnancy case was reported by a physician and describes the occurrence of ABORTION SPONTANEOUS (Miscarriage) and MATERNAL EXPOSURE DURING PREGNANCY (Maternal Exposure During Pregnancy) in a 28-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 3005789 and 3004234) for SARS-CoV-2 vaccination. No Medical History information was reported. On 26-Aug-2021, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 23-Sep-2021, received second dose of mRNA-1273 (Spikevax) (Intramuscular) dosage was changed to 1 dosage form. The patient''s last menstrual period was on 16-Aug-2021 and the estimated date of delivery was 23-May-2022. On 23-Sep-2021, after starting mRNA-1273 (Spikevax), the patient experienced MATERNAL EXPOSURE DURING PREGNANCY (Maternal Exposure During Pregnancy) (seriousness criterion medically significant). On 24-Sep-2021, the patient experienced ABORTION SPONTANEOUS (Miscarriage) (seriousness criterion medically significant). The patient received mRNA-1273 (Spikevax) beginning around the fifth week of the pregnancy. The delivery occurred on 24-Sep-2021, which was reported as Spontaneous Abortion. For foetus 1, The outcome was reported as Spontaneous Abortion NOS. At the time of the report, ABORTION SPONTANEOUS (Miscarriage) was resolving and MATERNAL EXPOSURE DURING PREGNANCY (Maternal Exposure During Pregnancy) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication reported. No treatment medication reported. Company Comment: This case concerns a 28-year-old, female patient with no relevant medical history, who experienced the unexpected events of maternal exposure during pregnancy and spontaneous abortion. The patient received the second dose of vaccine at 5 weeks of gestation. Spontaneous abortion occurred approximately 1 day after the second dose of mRNA-1273 (Spikevax). The benefit-risk relationship of mRNA-1273 (Spikevax) is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 11-Oct-2021: Translated document received on 13-Oct-21. No new information.; Sender''s Comments: This case concerns a 28-year-old, female patient with no relevant medical history, who experienced the unexpected events of maternal exposure during pregnancy and spontaneous abortion. The patient received the second dose of vaccine at 5 weeks of gestation. Spontaneous abortion occurred approximately 1 day after the second dose of mRNA-1273 (Spikevax). The benefit-risk relationship of mRNA-1273 (Spikevax) is not affected by this report.


VAERS ID: 1834885 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-27
Onset:2021-09-23
   Days after vaccination:239
Submitted: 0000-00-00
Entered: 2021-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ 6136 / 2 - / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Non-smoker
Allergies:
Diagnostic Lab Data:
CDC Split Type: HRPFIZER INC202101435310

Write-up: Missed abortion; This is a spontaneous report from a contactable consumer or other non hcp downloaded from the Regulatory Authority, regulatory authority number HR-HALMED-300051238. A 32-year-old pregnant female patient received the second dose of BNT162B2 (Lot Number: EJ 6136), intramuscular on 27Jan2021 as 0.3 mL single for COVID-19 immunisation. The patient''s medical history included non-smoker. The patient''s concomitant medications were not reported. The patient previously received the first dose of BNT162B2 (Lot Number: EL1491), intramuscular on 06Jan2021 as 0.3 mL for COVID-19 immunisation. The patient experienced missed abortion on 23Sep2021. The mother reported she became pregnant while taking BNT162B2. The mother was 11 weeks pregnant at the onset of the event. The outcome of the event was unknown. Reporter''s comments: I was told by gynecology experts that the 80 percent of aborted pregnancies given to young (healthy) girls concern vaccinated women. I am asking on the same tame as a doctor on clinical hospital i.e. the person who was pressured, and will again be pushed for the 3rd dose, for vaccination; and I have implemented all the vaccines in an orderly manner so far to dutifully investigate and then create a database of side effects on COVID-19 abortions that will be transparent for users. Probably, many cases have not been reported, because (until pregnancy occurs, and then to know about the death of the baby) it must take some time. Relevant medical history: so far without a history of miscarriage, I do not smoke or have allergies Reaction / event as reported by initial reporter: cessation of beating of the child''s heart, growth delay. Result of Assessment: BNT162B2/ event(s): Unlikely No follow-up attempts possible. No further information expected.; Sender''s Comments: Linked Report(s) : HR-PFIZER INC-202101444072 foetal case


VAERS ID: 1732844 (history)  
Form: Version 2.0  
Age: 24.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-09-14
Onset:2021-09-24
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-09-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30130BA / 1 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Foetal death, Ultrasound foetal abnormal, Uterine dilation and curettage
SMQs:, Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Progesterone in oil, prenatals, estrace
Current Illness: n/a
Preexisting Conditions: n/a
Allergies: rash when taking amoxicillin
Diagnostic Lab Data: D&C will be performed
CDC Split Type:

Write-up: Pregnant, due date April 30th. No issues at all and heartbeat had already been detected 9/10. Received vaccine 9/14 and on 9/24 ultrasound showed baby had stopped developing a week prior.


VAERS ID: 1793615 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: California  
Vaccinated:2021-09-24
Onset:2021-09-24
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-10-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2587 / 1 LA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Dysgeusia, Exposure during pregnancy, Feeling cold, Headache, Hypoaesthesia
SMQs:, Peripheral neuropathy (broad), Taste and smell disorders (narrow), 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), Sexual dysfunction (broad)

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

Write-up: Unknown pregnancy at the time of shot. Found out a week later that I was 3 weeks pregnant. Left side of body went completely numb, couldn''t feel toes or fingers. Went really cold on left side of body all within 20 mins of shot. Metal taste in mouth. Lasted 24 hours. Instantly after recieve shot. Slept for 5 hours once I was able to get home. Consistent headache for 2 weeks after shot and I don''t ever get headaches. Lost baby at 3 1/2 weeks after trying for a whole year to get pregnant. Since had a headache after loss of baby for a week.


VAERS ID: 1826118 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-07-26
Onset:2021-09-24
   Days after vaccination:60
Submitted: 0000-00-00
Entered: 2021-10-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FD0932 / 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: Medical History/Concurrent Conditions: Abortion spontaneous; Comments: The patient had no other reported health issues
Allergies:
Diagnostic Lab Data:
CDC Split Type: DKPFIZER INC202101379423

Write-up: Spontaneous abortion 9+5. First day of last menstruation was 17Jul; This is a spontaneous report from a contactable consumer regulatory authority, report number DK-DKMA-WBS-0089110. A 31-year-old female patient received bnt162b2 (COMIRNATY), via an unspecified route of administration on 26Jul2021 (Batch/Lot Number: FD0932; Expiration Date: 30Sep2021) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included abortion spontaneous from 2019 to 2019. The patient had no other reported health issues. The patient''s concomitant medications were not reported. The patient experienced spontaneous abortion 9+5, first day of last menstruation was 17Jul on 24Sep2021. Also reported maternal exposure during pregnancy, first trimester (9+5) on 26Jul2021. The mother reported she became pregnant while taking bnt162b2. The mother was 9 Weeks pregnant at the onset of the event. The event was reported as medically significant. The outcome of the event was not recovered. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1734681 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Illinois  
Vaccinated:2021-09-04
Onset:2021-09-25
   Days after vaccination:21
Submitted: 0000-00-00
Entered: 2021-09-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 004F21A / 1 LA / IM

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

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

Write-up: Patient miscarried in the 11 days following vaccine administration. Patient does have a history of miscarriage.


VAERS ID: 1761696 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-09-24
Onset:2021-09-25
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-10-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3004215 / 2 RA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Chills, Maternal exposure during pregnancy, Pyrexia, Ultrasound antenatal screen, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: No
Current Illness: No
Preexisting Conditions: No
Allergies: No
Diagnostic Lab Data: Sonogram showing baby inside of uterus with heartbeat on 09/25. Then, 09/26 morning I had a miscarriage.
CDC Split Type:

Write-up: Slight fever and chills. Spotting. Miscarriage.


VAERS ID: 1773454 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: California  
Vaccinated:2021-09-24
Onset:2021-09-25
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-10-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011D21A / 2 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood test abnormal, Dyspnoea, Echocardiogram abnormal, Exposure during pregnancy, Hepatic enzyme increased, Induced labour, Inflammatory marker increased, Pericarditis, Premature delivery
SMQs:, Liver related investigations, signs and symptoms (narrow), Anaphylactic reaction (broad), Systemic lupus erythematosus (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Chronic kidney disease (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 7 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: None
Current Illness: No
Preexisting Conditions: No
Allergies: Moxifloxacin
Diagnostic Lab Data: So much blood work. Inflammation markers were high but seems normal that late in pregnancy. Liver enzymes with 100+ (AST/ALT) and that seems to concern doctors the most of all the blood work.
CDC Split Type:

Write-up: Woke up the morning of 9/25 with trouble breathing. This was ~19 hours after 2nd dose. Held off for a day and checked myself into ER. Cardiologist at ER diagnosed me with acute pericarditis and sent me home without meds since the meds typically used to treat acute pericarditis are not used for pregnant women. On Monday 9/27 I had a 34 week OB-GYN checkup. Doctor saw me and urged me to go to the hospital where she delivers as soon as possible. My husband and I drove to Hospital. Was checked into ER and sent to the Telemetry department. Dr''s there did blood work and an echocardiogram and confirm that I have acute pericarditis. Was advised to deliver baby ASAP so that the appropriate meds can be used to help my symptoms. Was induced and gave birth on 10/1 to a baby 34 weeks and 5 days old.


VAERS ID: 1797484 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: South Dakota  
Vaccinated:2021-08-04
Onset:2021-09-25
   Days after vaccination:52
Submitted: 0000-00-00
Entered: 2021-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FA7484 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2587 / 2 LA / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamins, tylenol as needed
Current Illness: Pregnancy
Preexisting Conditions: N/A
Allergies: NKA
Diagnostic Lab Data: Ultrasound- 9/24/21. Quantitative HCG 21,011. Quantitative HCG 2,922 10/1. D& C 10/11.
CDC Split Type:

Write-up: I received my first covid vaccine not knowing I was pregnant. My last mensural period was July 17,2020. I received my first shot on 8/4/21 and was advised to get my second shot knowing I was in my first trimester. . On 9/9 I had my first ultrasound with a due date of May 5, 2022. The baby was showing to be slightly smaller measuring 6 weeks 1 day instead of 7 weeks 6 days but did have a heart beat I received my second shot on 9/22/21. I went back for another ultrasound on 9/24/21. The baby had stopped growing and lost his/her heartbeat between the two ultrasounds. I had a miscarriage.


VAERS ID: 1751270 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-07-09
Onset:2021-09-25
   Days after vaccination:78
Submitted: 0000-00-00
Entered: 2021-10-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC202101266333

Write-up: miscarriage; Miscarriage of pregnancy; This is a spontaneous report from a contactable consumer received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202109251419572670-XC0DW, Safety Report Unique Identifier GB-MHRA-ADR 25995812. A 35-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on 09Jul2021 (Lot Number and expiry date was not reported) as single dose for COVID-19 immunisation. Medical history included pregnancy from an unknown date and unknown if ongoing Patient no longer pregnant at the time of reporting. Concomitant medication included folic acid (FOLIC ACID) taken for vitamin supplementation, start and stop date were not reported. Patient was not currently breastfeeding. Patient was not enrolled in clinical trial. Patient had previous pregnancy successful. The patient had received patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on 12May2021 (Lot Number and expiry date was not reported) as single dose for COVID-19 immunisation. The patient experienced miscarriage on an unspecified date. The patient experienced miscarriage of pregnancy on an 25Sep2021. The events considered as medically significant and had hospitalization. The patient underwent lab tests and procedures which included sars-cov-2 test negative on No - Negative COVID-19 test. Patient was not had symptoms associated with COVID-19. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1764141 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-20
Onset:2021-09-25
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-10-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 3004223 / 2 - / OT

Administered by: Unknown       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: GBMODERNATX, INC.MOD20213

Write-up: Miscarriage; Maternal exposure during pregnancy; This case was received via regulatory authority (Reference number: GB-MHRA-ADR 26000857) on 28-Sep-2021 and was forwarded to Moderna on 28-Sep-2021. This regulatory authority prospective pregnancy case was reported by a physician and describes the occurrence of ABORTION SPONTANEOUS (Miscarriage) in a female patient of an unknown age who received mRNA-1273 (Moderna CoviD-19 Vaccine) (batch no. 3004223) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 20-Sep-2021, the patient received second dose of mRNA-1273 (Moderna CoviD-19 Vaccine) (unknown route) 1 dosage form. Last menstrual period and estimated date of delivery were not provided. On 25-Sep-2021, the patient experienced ABORTION SPONTANEOUS (Miscarriage) (seriousness criterion medically significant). 25-Sep-2021, the patient experienced MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy). At the time of the report, ABORTION SPONTANEOUS (Miscarriage) was resolving and MATERNAL EXPOSURE DURING PREGNANCY (Maternal exposure during pregnancy) had resolved. The action taken with mRNA-1273 (Moderna CoviD-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna CoviD-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications not reported. Treatment information not provided. This case concerns a female patient, unknown age, with no known medical history, who experienced the unexpected events of maternal exposure during pregnancy and spontaneous abortion. The patient received the second dose of vaccine at unknown weeks of gestation. Spontaneous abortion occurred 5 days after the second dose of Moderna vaccine. The benefit-risk relationship of Moderna vaccine is not affected by this report.; Sender''s Comments: This case concerns a female patient, unknown age, with no known medical history, who experienced the unexpected events of maternal exposure during pregnancy and spontaneous abortion. The patient received the second dose of vaccine at unknown weeks of gestation. Spontaneous abortion occurred 5 days after the second dose of Moderna vaccine. The benefit-risk relationship of Moderna vaccine is not affected by this report.


VAERS ID: 1826120 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-08-06
Onset:2021-09-25
   Days after vaccination:50
Submitted: 0000-00-00
Entered: 2021-10-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC5029 / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Biopsy placenta, Blood test, Body mass index, Culture urine
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 2021; Test Name: Biopsy placenta; Result Unstructured Data: Test Result:foetal placenta tissue for genetic examine array; Comments: CGH; Test Date: 2021; Test Name: Blood test; Result Unstructured Data: Test Result:TORCH test, no result; Test Name: Body mass index; Result Unstructured Data: Test Result:31; Test Date: 2021; Test Name: Culture urine; Result Unstructured Data: Test Result:No result
CDC Split Type: DKPFIZER INC202101454181

Write-up: Spontaneous abortion in gestation age 15 week; This is a spontaneous report received from a contactable other healthcare professional (HCP). This is the second of two reports. The first report is a report from the regulatory authority (regulatory authority report number: DK-DKMA-WBS-0089108). A 30-year-old female patient received the second dose of bnt162b2 (COMIRNATY), intramuscular on 06Aug2021 (Lot Number: FC5029; Expiration Date: 31Oct2021) as DOSE 2, SINGLE for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously received the first dose of bnt162b2 (COMIRNATY), on 09Jul2021 (Lot number: FE2090) as DOSE 1, SINGLE for COVID-19 immunisation in which she experienced hemorrhage in pregnancy. The patient experienced spontaneous abortion in gestation age 15 week on 25Sep2021. The mother reported she was pregnant when she received bnt162b2. The mother was 15 Weeks pregnant at the onset of the event. The patient underwent lab tests and procedures which included biopsy placenta: foetal placenta tissue for genetic examine array on 2021 CGH, blood test: torch test, no result on 2021, body mass index: 31 on unknown date, culture urine: no result on 2021. The patient did not receive any corrective treatment. Outcome of the event was recovered on 25Sep2021. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : DK-PFIZER INC-202101314312 Same reporter, patient, drug, and different dose/event


VAERS ID: 1841091 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-09-25
Submitted: 0000-00-00
Entered: 2021-11-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202101402480

Write-up: Stillbirth; Fatigue; This is a spontaneous report from a contactable other health professional via the regulatory authority. Regulatory authority report number is 642560. As per source A 38-years-old female patient received bnt162b2 (COMIRNATY), unknown dose number via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as a single dose,for covid-19 immunization. Medical history and concomitant medications were not reported. On 25Sep2021, the patient experienced stillbirth and fatigue. The outcome of the events was not reported. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1736815 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-09-23
Onset:2021-09-26
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-09-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Blood fibrinogen decreased, Exposure during pregnancy, Foetal death, Foetal heart rate abnormal, Foetal hypokinesia, International normalised ratio abnormal, Prothrombin level abnormal, Ultrasound antenatal screen abnormal
SMQs:, Liver-related coagulation and bleeding disturbances (narrow), Haemorrhage laboratory terms (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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: Gestational diabetes
Allergies: Penicillin
Diagnostic Lab Data: Coagulation panel showed critically low fibrinogen, abnormal findings for PT and INR. Pt transferred to higher level of care for treatment of possible disseminated intravascular coagulation.
CDC Split Type:

Write-up: Pt came to hospital for decreased fetal movement. Ultrasound verified no cardiac activity in fetus, diagnosed intrauterine fetal demise at 34 weeks, 2 days gestation. Pt reported she had received her second covid vaccine on 9/23/21, after it was mandated for her job. She reported last feeling baby move on 9/25/21.


VAERS ID: 1741785 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Hawaii  
Vaccinated:2021-08-10
Onset:2021-09-26
   Days after vaccination:47
Submitted: 0000-00-00
Entered: 2021-09-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0187 / 1 RA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0217 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Antiphospholipid antibodies, Antiphospholipid antibodies negative, Beta 2 microglobulin, Cardiolipin antibody, Delivery, Exposure during pregnancy, Foetal death, Foetal hypokinesia, Gene mutation identification test, Glycosylated haemoglobin decreased, Induced labour, Kleihauer-Betke test negative, Pathology test, SARS-CoV-2 test negative, Treponema test negative
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: None
Preexisting Conditions: Chronic hypertension
Allergies: None
Diagnostic Lab Data: Hemoglobin a1c 5.1% Negative Kleihauer-Betke test. SARS-COV-2: negative PCR on admission (9/26) Negative syphilis testing, negative Lupus anticoagulant, phospholipid antibody panel, beta 2 microglobin, cardiolipin antibody tests all pending. Placental pathology pending, fetal autopsy and microarray genetic studies pending.
CDC Split Type:

Write-up: Pregnancy history: Gravida 2, Para 1 (previous cesarean section at 42 weekS) Estimated date of delivery: 11/16/21 based on LMP consistent with 8wk ultrasound Vaccinated with Pfizer COVID vaccine on 8/10 (1st shot of series), patient pregnant at 26+0 weeks gestation. Vaccinated with Pfizer COVID vaccine on 8/31 (2nd shot of series), patient pregnant at 29+0 weeks gestation. Patient presented with decreased fetal movement on 9/26/21 and was diagnosed with intra-uterine fetal demise. Labor induced with subsequent vaginal delivery. Demised infant weighing 1673 grams.


VAERS ID: 1790868 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Louisiana  
Vaccinated:2021-09-16
Onset:2021-09-26
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-10-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FP8448 / 2 LA / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101285693

Write-up: Confirmed Miscarriage; This is a spontaneous report from a contactable nurse (patient). A 29-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Left on 16Sep2021 07:15 (Lot Number: FP8448) at the age of 29-year-old, as dose 2, single for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. No other vaccine was administered in four weeks. The patient did not have COVID-19 prior to vaccination and was not tested for COVID-19 post vaccination. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number=FP8448) via an unspecified route of administration, administered in Arm Left on 26Aug2021 at 08:00 AM at the age of 29-year-old at single dose for COVID-19 immunisation. The patient had confirmed miscarriage on 26Sep2021. The event resulted in Doctor or other healthcare professional office/clinic visit. No treatment was received. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Based on the current limited available information and the drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of event Abortion spontaneous cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1804392 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Maryland  
Vaccinated:2021-09-16
Onset:2021-09-26
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FO3184 / 1 RA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30135BA / 2 RA / SYR

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

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

Write-up: Miscarriage at 22 weeks. No fetal heartbeat after first Covid shot. Had to give birth to still born baby.


VAERS ID: 1845496 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: Missouri  
Vaccinated:2021-09-23
Onset:2021-09-26
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal cardiac arrest, Stillbirth
SMQs:, Congenital and neonatal arrhythmias (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? 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: Celexa 10mg Protonix 40mg Vitamin B6 Unisom Pepcid
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: Penicillin, terbinafine
Diagnostic Lab Data:
CDC Split Type:

Write-up: Was 33weeks and 6 days pregnant on 9/23/21 that morning I had a non stress test done to monitor my baby as I got them done twice weekly and she was perfectly fine. I got my second covid vaccine that afternoon. Sometime after that and sunday morning my babies heart stopped beating and I had to deliver her stillborn. The autopsy and placenta pathology came back normal. Vaccine is only cause.


VAERS ID: 1780395 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2021-08-21
Onset:2021-09-26
   Days after vaccination:36
Submitted: 0000-00-00
Entered: 2021-10-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE3380 / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Clinical trial participant
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC202101280730

Write-up: Miscarriage; This is a spontaneous report from a contactable physician received from the Regulatory Authority (UK-MHRA). The regulatory authority report number is GB-MHRA-WEBCOVID-202109271718117680-0GTPZ. Safety Report Unique Identifier GB-MHRA-ADR 26000930. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Batch/Lot Number: fe3380), dose 2 via an unspecified route of administration on 21Aug2021 as dose 2, single for covid-19 immunization. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection) for covid-19 immunization. Medical history included clinical trial participant from an unknown date and unknown if ongoing. The patient''s concomitant medications were not reported. Patient has not had symptoms associated with COVID-19 Not had a COVID-19 test. On 26Sep202, the patient experienced miscarriage (medically significant). The outcome of event was resolving. No Follow-up attempts are needed. No further information is expected.


VAERS ID: 1809465 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-07-31
Onset:2021-09-26
   Days after vaccination:57
Submitted: 0000-00-00
Entered: 2021-10-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FD8813 / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID; INFANRIX IPV HIB
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Allergy; Hay fever; Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test; Test Name: scans; Result Unstructured Data: Test Result:Foetal abnormalities were found including facial; Comments: Foetal abnormalities were found including facial cleft, cleft lip, cleft palate, underdeveloped eye
CDC Split Type: GBPFIZER INC202101341902

Write-up: loss of pregnancy; This is a spontaneous report from a contactable consumer. This is a report received from the Regulatory Agency (RA). Regulatory authority report number is GB-MHRA-WEBCOVID-202110071735531460-SFBTE. Safety Report Unique Identifier is GB-MHRA-ADR 26049745. This consumer reported information for both mother and fetus. This is the maternal report. A 32-years-old female patient received bnt162b2 (BNT162B2), via an unspecified route of administration on 09Jun2021 (Batch/Lot Number: EW3143) as dose 1, single and via an unspecified route of administration on 31Jul2021 (Batch/Lot Number: FD8813) as dose 2, single for Covid-19 immunisation . Medical history included allergy, pregnancy from an unknown date and unknown if ongoing (patient no longer pregnant at the time of reporting), and hayfever. Patient was medically fit and well. Patient has not had symptoms associated with COVID-19. Patient is not currently breastfeeding. Patient is not enrolled in clinical trial. Concomitant medications included folic acid taken for folic acid supplementation, start and stop date were not reported; diphtheria vaccine toxoid, hib vaccine conj, pertussis vaccine acellular 3-component, polio vaccine inact 3v (vero), tetanus vaccine toxoid (INFANRIX IPV HIB) taken for an unspecified indication, start and stop date were not reported. The patient previously took erythromycin and experienced allergy. The patient experienced loss of pregnancy on 26Sep2021 with outcome of unknown. The patient underwent lab test and procedures which included Covid-19 virus test: no-Covid-19 test on unknown date, scans: foetal abnormalities were found including facial on unknown date. Foetal abnormalities were found including facial cleft, cleft lip, cleft palate, underdeveloped eye. pregnancy was subsequently lost in the second trimester. Patient has not tested positive for COVID-19 since having the vaccine. Additional information: I had the vaccines during the first trimester and a foetal abnormality (resulting in loss of pregnancy) was found. I am concerned it was a result of having the vaccine at such a sensitive time in the pregnancy. An autopsy is being carried out.Did the medicine have an adverse effect on any aspect of the pregnancy: Yes. Pregnancy adverse effects details: Foetal abnormality, potentially related. Details of previous pregnancies: Previous healthy baby boy, born at term. This pregnancy was very restful, but abnormality was found and pregnancy was subsequently lost in the second trimester. Patient was exposed to the medicine first-trimester (1-12 weeks). Details of scans or investigations: Foetal abnormalities were found including facial cleft, cleft lip, cleft palate, underdeveloped eye, more results pending, and will follow after autopsy. Relevant investigations or tests conducted: "Autopsy of foetus will occur but results have not yet been given." No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : GB-PFIZER INC-202101355068 babycase


VAERS ID: 1809976 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-16
Onset:2021-09-26
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-10-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FH4092 / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: ADAMTS13 activity assay, Antiphospholipid antibodies, Foetal death, Investigation, Thrombotic thrombocytopenic purpura
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Embolic and thrombotic events, arterial (narrow), Renovascular disorders (broad), Termination of pregnancy and risk of abortion (narrow), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Hypothyreosis; Spontaneous abortion (3 former spontaneous abortions in 1 trimester); Vitiligo
Allergies:
Diagnostic Lab Data: Test Date: 20210926; Test Name: ADAMTS13 activity assay; Result Unstructured Data: Test Result:Severly reduced; Comments: Severly reduced ADAMTS13 activity, diagnostic for thrombotic thrombocytopenic purpura.; Test Date: 2021; Test Name: Antiphospholipid antibodies; Result Unstructured Data: Test Result:Negative; Test Date: 20210926; Test Name: Investigation; Result Unstructured Data: Test Result:had debut of neurological symptoms; Comments: the same day as intrauterine death was established
CDC Split Type: NOPFIZER INC202101384632

Write-up: DEATH INTRAUTERINE (22+3 WEEKS); THROMBOTIC THROMBOCYTOPENIC PURPURA; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority-WEB, regulatory authority number [NO-NOMAADVRE-FHI-2021-Uwjngg] and [NO-NOMAADVRE-E2B_00054246]. A 35-year-old pregnant female patient received bnt162b2 (COMIRNATY), intramuscular on 16Sep2021 (Lot Number: FH4092) as dose number unknown, single for COVID-19 immunization. Medical history included vitiligo, hypothyreosis and spontaneous abortion (three former spontaneous abortions in 1 trimester, but the patient had no history of illness in conjunction with these). The patient''s concomitant medications were not reported. On 26Sep2021, the patient developed thrombotic thrombocytopenic purpura and death intrauterine. The mother reported she became pregnant while taking bnt162b2. The mother was 22 Weeks pregnant at the onset of the event. The fetal outcome is intrauterine death. Course of events: The patient had experienced signs of reduced foetal life a few days after vaccination. Contacted gynecologist which stated that foetal heart action was ok. patient again contacted gynecologist due to lack of foetal signs of life. The gynecologist determined intrauterine foetal death, week 22+3. Investigation on 26Sep2021: the patient had debut of neurological symptoms the same day as intrauterine death was established. Established intravascular haemolysis and severe thrombocytopenia. On 26Sep2021, severely reduced ADAMTS13 activity, diagnostic for thrombotic thrombocytopenic purpura. Negative for antiphospholipid syndrome on unspecified date in 2021. The reported events resulted in Physician office visit. Therapeutic measure was taken as a result of thrombotic thrombocytopenic purpura which included daily plasmapheresis, high-dose steroids, rituximab. The outcome of the events was not recovered. The events were considered serious (Life Threatening, Other Serious (Important Medical Events)). The RA assessed the causality of the events with bnt162b2 (COMIRNATY) as possible. Reporter comments: The patient was started on treatment for thrombotic thrombocytopenic purpura from the day of the admission with daily plasmapheresis, high-dose steroids, rituximab. The situation for the patient was still critical at day 9 of the treatment. 08Oct2021 and 12Oct2021, RA: Additional information received from hospital by phone. They consider it likely that thrombotic thrombocytopenic purpura has been triggered by the pregnancy in itself, and that it is unlikely to be caused by vaccination. However, due to temporal relationship, they decided to report it. The patient was still in hospital on 12Oct2021. An autopsy will be performed on the foetus. 13Oct2021 RA: requested additional information. If new medical information is received, report will be updated. No follow-up attempts are possible. No further information is expected.; Reporter''s Comments: Summary of Reporter Comment: The patient was started on treatment for thrombotic thrombocytopenic purpura from the day of the admission with daily plasmapheresis, high-dose steroids, rituximab. The situation for the patient was still critical at day 9 of the treatment.


VAERS ID: 1855116 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-09-26
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: no other drugs, no underlying diseases.
Allergies:
Diagnostic Lab Data:
CDC Split Type: ATJNJFOC20211117124

Write-up: ABORTION; This spontaneous pregnancy report received from a physician via a Regulatory Authority [regulatory authority, AT-BASGAGES-2021-059340] concerned a 30 year old female. The patient''s weight was 64 kilograms, and height was 168 centimeters. The patient''s pre-existing medical conditions included: no other drugs, no underlying diseases. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: XD985 expiry: UNKNOWN) 1 dosage forms, 1 total, administered on 10-JUN-2021 for covid-19 vaccination. No concomitant medications were reported. On 26-SEP-2021, the patient had abortion. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from abortion. This report was serious (Other Medically Important Condition).


VAERS ID: 1738627 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: New York  
Vaccinated:2021-05-04
Onset:2021-09-27
   Days after vaccination:146
Submitted: 0000-00-00
Entered: 2021-09-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1808609 / UNK - / -

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

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

Write-up: Patient received vaccine on May 4th. She was 9 weeks pregnant. In June she had a miscarriage. September 27 pt is admitted to hospital with PE.


VAERS ID: 1801937 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-27
Onset:2021-09-27
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-10-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Blood glucose decreased, Hypotension, Loss of consciousness, Malaise, Nausea, Ultrasound antenatal screen
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Termination of pregnancy and risk of abortion (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (narrow), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none.
Allergies:
Diagnostic Lab Data: Test Name: ultrasound; Result Unstructured Data: Test Result: baby had healthy heart beat and growing perfectly; Comments: at 6 weeks 4 days; Test Date: 20211005; Test Name: ultrasound; Result Unstructured Data: Test Result: No heartbeat detected; Comments: Baby stopped growing from 27Aug2021 at 8 weeks.
CDC Split Type: AUPFIZER INC202101333544

Write-up: low blood pressure; low blood sugar; nausea; unconscious; I had a missed miscarriage the same day I received the Dose 2 Pfizer; I was sick the same day; This is a spontaneous report from a contactable consumer on behalf of self (patient) received via Regulatory Authority. A 39-years-old female patient received bnt162b2 (COMIRNATY), dose 2 via an unspecified route of administration, administered in left arm on 27Sep2021 at 11:15 at age of 39-years-old (Batch/Lot number was not reported) as single dose for covid-19 immunisation. There was no medical history or concomitant medication. Prior to vaccination, the patient was not diagnosed with COVID-19. No known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medications within 2 weeks of vaccination. The patient previously received bnt162b2 (COMIRNATY) dose 1 via an unspecified route of administration, administered in left arm on 17Aug2021 12:15 AM for covid-19 immunisation. The patient was pregnant with gestational period: 8 weeks. Last menstrual date was 31Jul2021 and delivery date was 09May2022. The patient had a missed miscarriage the same day she received the dose 2 on 27Sep2021 at 13:00. She was not aware she had miscarried until 05Oct2021 when an ultrasound confirmed my baby stopped growing from 27Sep21 at 8 weeks the same day as dose 2. No heart beat was detected on 05Oct2021. The patient had an ultrasound at 6 weeks 4 days and baby had healthy heart beat and was growing perfectly. The patient also collapsed and blacked-out the on 28Sep2021 at 11.15am day after dose2. She was rushed via ambulance to hospital. She was unconscious for 10 seconds or so on 28Sep2021 at 11.15am. Hospital reported low blood pressure and blood sugar with nausea symptoms. This was all from the dose 2 vaccine. The patient had no issues or symptoms before dose 2 and her baby was healthy. Her = baby was healthy and only stopped growing on 27Sep21 by accurate ultrasound (can be provided) when dose 2 was administered. The patient was sick the same day as dose 2 was given to her and felt ill the entire week. The patient was unaware her baby had died and that she miscarried on this day. The adverse event result in Emergency room/department or urgent care. The patient was on a drip with fluids and anti nausea. The patient was hospitalized for 1 day. The outcome of the events was not recovered. Since the vaccination, the patient had not been tested for COVID-19.


VAERS ID: 1822072 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-23
Onset:2021-09-27
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202101361551

Write-up: Abortion spontaneous; This is a spontaneous report from a contactable health professional via the Regulatory Authority. Regulatory authority report number: 639118. A 27-years-old female patient received bnt162b2 (COMIRNATY), via an unspecified route of administration on 23Sep2021 (Batch/Lot number was not reported) as dose number unknown, as a single dose for COVID-19 immunisation. Relevant medical history and concomitant medication were not provided. On 27Sep2021, the patient experienced abortion spontaneous. The outcome of the event was recovered on an unspecified date in 2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1858826 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-27
Onset:2021-09-27
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Blood glucose, Blood glucose decreased, Hypotension, Loss of consciousness, Malaise, Nausea
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Termination of pregnancy and risk of abortion (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (narrow), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210927; Test Name: blood glucose; Result Unstructured Data: Test Result:decreased
CDC Split Type: AUPFIZER INC202101453001

Write-up: Abortion spontaneous; Loss of consciousness; Blood glucose decreased; Hypotension; Malaise; Nausea; This is a spontaneous report from a contactable other health professional received from the Regulatory Authority. The regulatory authority report number is 648045. A 39-year-old female patient received BNT162B2 (COMIRNATY Solution for injection), via an unspecified route of administration, on 27Sep2021 (lot number not reported), at age 39 years old, as dose number unknown, single, for COVID-19 immunisation. The patient was pregnant at the time of vaccination. Relevant medical history and concomitant medications were not reported. On 27Sep2021, the patient experienced abortion spontaneous, loss of consciousness, blood glucose decreased, hypotension, malaise and nausea. The outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1756886 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: Arizona  
Vaccinated:2021-08-21
Onset:2021-09-28
   Days after vaccination:38
Submitted: 0000-00-00
Entered: 2021-10-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion missed, Exposure during pregnancy, Foetal heart rate abnormal, Ultrasound foetal abnormal, Ultrasound scan vagina abnormal
SMQs:, Malignancy related therapeutic and diagnostic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, prenatal probiotic, prenatal omega 3, cetirizine, melatonin
Current Illness: None
Preexisting Conditions: None
Allergies: Latex (rash)
Diagnostic Lab Data: 9/28/21- abdominal ultrasound x1, intravaginal ultrasound x2 with no cardiac activity noted- missed abortion
CDC Split Type:

Write-up: Newly pregnant during vaccination, with EDD 4/29/22. Normal ultrasound at 8 weeks (9/16/21) with developing fetus and yolk sac observed with heart rate measured at 164 bpm. Two weeks later (9/28/21), no cardiac activity seen x 3 ultrasounds; estimated fetal size ~9 weeks, suggesting demise one week prior.


VAERS ID: 1857618 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Illinois  
Vaccinated:2021-05-10
Onset:2021-09-28
   Days after vaccination:141
Submitted: 0000-00-00
Entered: 2021-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 040B21A / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Human chorionic gonadotropin, Maternal exposure before 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? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Lomita, Spironolactone, Naci, prenatal vitamin, Magnesium, Turmeric, Vitamin C and Vitamin D3
Current Illness: n/a
Preexisting Conditions: bipolar depression, PCOS
Allergies: Clonidine''s family medication
Diagnostic Lab Data: blood work ultra sound
CDC Split Type: vsafe

Write-up: I was 12 weeks pregnancy and I had a miscarriage. The symptoms of the miscarriage started on Sept. 28th and I did not know that I was having a miscarriage. On October 01, It was confirmed that I did have a miscarriage. I was in ER. They ran and HCG level and did a abdominal ultra sound.


VAERS ID: 1844758 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-28
Onset:2021-09-28
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Immunisation, Lethargy, Maternal exposure during pregnancy, Off label use, Pyrexia, SARS-CoV-2 test
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (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), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (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: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: COVID-19; Folic acid supplementation; Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Date: 20210828; Test Name: COVID-19 virus test; Test Result: Positive ; Comments: Yes - Positive COVID-19 test
CDC Split Type: GBPFIZER INC202101417947

Write-up: Miscarriage of pregnancy; lethargy; fever; Maternal exposure during pregnancy; Booster; Off label dose; This is a spontaneous report from a contactable consumer or other non-healthcare professional received from a Regulatory Authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202110202045279620-A8VWB. Safety Report Unique Identifier GB-MHRA-ADR 26100663. A 31-years-old pregnant female patient received bnt162b2 (COMIRNATY, Solution for injection; Batch/Lot number was not reported), dose 3 via an unspecified route of administration on 28Sep2021 as DOSE 3 (BOOSTER), SINGLE (at age of 31-years) for covid-19 immunization (booster and off label dose). Medical history included pregnancy from an unknown date and not ongoing (patient no longer pregnant at the time of reporting) and folic acid supplementation from an unknown date, Covid-19 virus positive from 28Aug2021 to an unknown date. Concomitant medication included folic acid taken for folic acid supplementation, start and stop date were not reported. Patient has not had symptoms associated with COVID-19. Patient was not currently breastfeeding. Patient was not enrolled in clinical trial. The patient previously took first and second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection) as single dose for Covid-19 Immunization. The patient was exposed to vaccine during pregnancy on 28Sep2021. The patient experienced lethargy, and fever on 29Sep2021. The patient also presented with miscarriage of pregnancy on 30Sep2021. The mother reported she became pregnant while taking bnt162b2. The patient underwent lab tests and procedures which included sars-cov-2 test positive on 28Aug2021 Yes - Positive COVID-19 test. It was reported that, Fever, lethargy suffered day after vaccine, following day started to miscarry. The medicine has an adverse effect on any aspect of the pregnancy. The outcome of the events miscarriage of pregnancy recovered on 04Oct2021. The outcome of the events lethargy and fever was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1847932 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-06
Onset:2021-09-28
   Days after vaccination:22
Submitted: 0000-00-00
Entered: 2021-11-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / -

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

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: HCG levels; Result Unstructured Data: Test Result:HCG levels were high; Test Name: scan; Result Unstructured Data: Test Result:baby was measuring two weeks behind and the fetal; Comments: heart rate was only 58 bpm; Test Name: scan; Result Unstructured Data: Test Result:no fetal heart rate and the gestational sac; Comments: was collapsing
CDC Split Type: NZPFIZER INC202101418457

Write-up: Suffered a missed miscarriage; This is a spontaneous report from a contactable other hcp on behalf of self (patient) received via Regulatory Authority. This other hcp reported events for self (mother) and fetus. This is the maternal report. A 35-year-old pregnant female patient received BNT162B2 (COMIRNATY) (Batch/Lot number was not reported), dose 1, via an unspecified route of administration in the right arm on 06Sep2021 at 15:45 (at the age of 35-years-old) as DOSE 1, SINGLE for covid-19 immunisation. The patient''s medical history was not reported. Concomitant medication included folic acid (FOLIC ACID) taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. The pregnancy was reportedly going fine, HCG levels were high. The patient had her first dose of the vaccine and went for a scan 3 weeks later and the baby was measuring 2 weeks behind and the fetal heart rate was only 58 bpm. A second scan was performed 1 week later and there was no fetal heart rate and the gestational sac was collapsing. On 28Sep2021 at 10:30am, the patient suffered a miscarriage. The patient was hospitalized for miscarriage (abortion spontaneous) for 1 days. The mother was 7 Weeks pregnant at the onset of the event. The mother was due to deliver on 13May2022. The patient stated "the miscarriage did not happen naturally as my body did not recognize this which led to me being admitted to the hospital for a D&C. The patient underwent lab tests and procedures which included human chorionic gonadotropin (Unknown date): hcg levels were high, scan (Unknown date): baby was measuring two weeks behind and the fetal heart rate was only 58 bpm and scan (Unknown date): no fetal heart rate and the gestational sac was collapsing. Clinical outcome of the event was resolving. It was also reported that since the vaccination, the patient had not been tested for COVID-19. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up.; Sender''s Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal association between the event and suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.,Linked Report(s) : NZ-PFIZER INC-202101419136 same drug, same reporter; different event (mother/foetus case)


VAERS ID: 1852917 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-07-17
Onset:2021-09-28
   Days after vaccination:73
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Polycystic ovarian syndrome
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLPFIZER INC202101437946

Write-up: Miscarriage; Irregular bleeding. After miscarriage and 1 menstrual period, brown bleeding after 1.5 weeks; This is a spontaneous report from a contactable consumer or other non hcp downloaded from the regulatory authority-WEB, regulatory authority number NL-LRB-00694658. A 31 years old female patient received the first dose of BNT162B2 (COMIRNATY, Lot number unknown) at single dose for COVID-19 immunisation on 17Jul2021 (31 year old at the time of vaccination). Relevant history included Polycystic ovary syndrome. Relevant concomitant drug included folic acid oral suspension 1mg/ml, multivitamin with vitamin d capsule. The patient did not have previous COVID-19 infection. The patient had Irregular bleeding (irregular menstrual cycle) since 28Sep2021 following administration of BNT162B2. The patient had vaccination during pregnancy and miscarriage (other medically important condition) on unknown date. Irregular menstrual cycle: 2 months after start. Miscarriage: latency unknown. Maternal exposure during pregnancy: latency unknown. After miscarriage and 1 menstrual period, the patient had brown bleeding after 1.5 weeks. The patient has not recovered from irregular menstrual cycle. The outcome of other events was unknown. It was unknown at what pregnancy duration the vaccination and the miscarriage took place. Sender''s comments: Since the nature of the reported reaction does imply seriousness according to one of the CIOMS criteria, the reaction was considered as serious by the Pharmacovigilance Centre Lareb. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No follow-up attempts are possible.


VAERS ID: 1804502 (history)  
Form: Version 2.0  
Age: 22.0  
Sex: Female  
Location: Louisiana  
Vaccinated:2021-08-17
Onset:2021-09-29
   Days after vaccination:43
Submitted: 0000-00-00
Entered: 2021-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 040C21A / 2 LA / 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? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamins, vitamin D
Current Illness: none
Preexisting Conditions: Chronic HTN
Allergies: NKDA
Diagnostic Lab Data: Ultrasound OB transvaginal - Impression: Failed pregnancy with retained products of conception. Single intrauterine gestational sac with embryo crown-rump length measurement of 1.87cm, but no detectable cardiac flutter of cardiac activity.
CDC Split Type:

Write-up: Patient was pregnant. LMP 7/26/21 EDD- 5/2/22, patient went for dating sonogram on 9/29/21 , no detectable cardiac flutter or cardiac activity.


VAERS ID: 1814604 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-09-24
Onset:2021-09-29
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 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? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Vita Fusion Pre-Natal
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: D&C Scheduled for 10/26
CDC Split Type:

Write-up: Received vaccine on a Friday. Ultrasound the following Wednesday showed fetal pole with no heartbeat measuring 5 weeks and 6 days. Had follow up ultrasounds on 10/6 and 10/11 showing no growth.


VAERS ID: 1795684 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-23
Onset:2021-09-29
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-10-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 1H048A / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC202101314389

Write-up: Intra-uterine death; This is a spontaneous report from a non-contactable physician downloaded from the Agency Regulatory Authority-WEB, regulatory authority number DE-PEI-202100200925. A 36-years-old female patient received bnt162b2 (COMIRNATY), dose 1 via an unspecified route of administration on 23Sep2021 (Batch/Lot Number: 1H048A) as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history was not reported. The patient''s concomitant medications were not reported. The patient experienced intra-uterine death on 29Sep2021. The event was reported as serious with hospitalization and disability. Outcome of event was unknown. Event assessment : Comirnaty/ event /RA /Result of Assessment: D. Unclassifiable No follow-up attempts are possible. No further information is expected.


VAERS ID: 1848781 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: California  
Vaccinated:2021-08-12
Onset:2021-09-30
   Days after vaccination:49
Submitted: 0000-00-00
Entered: 2021-11-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / 1 RA / SYR

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

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Pre-natal vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: Penicillin
Diagnostic Lab Data: 3 ultrasounds, first at 12 weeks along. All demonstrating severe heart defects. Had to terminate the pregnancy.
CDC Split Type:

Write-up: Received shot at 5 weeks pregnant. During the time the heart is being formed in the fetus. Fetus was formed with severe heart defects.


VAERS ID: 1849154 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: New York  
Vaccinated:2021-09-29
Onset:2021-09-30
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-11-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK - / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain upper, Abortion spontaneous, Blood test, Exposure during pregnancy, Human chorionic gonadotropin, Muscle spasms, Pain, Pregnancy test positive, Progesterone, Tearfulness, Ultrasound scan
SMQs:, Acute pancreatitis (broad), Dystonia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), 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), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: HGC and Progesterone blood tests, sonograms
CDC Split Type:

Write-up: I found out I was pregnant four days before getting the Covid Vaccine. I wa a mandated to get the vaccine or lose my job. I got on that Wednesday. At 1:00am in the morning until Friday evening. I had very bad cramping and stomach pains I was in tears. I took another orinagncy test and was still pregnant. I went to the dr. The following week and I was only 1/2 weeks pregnant when I have already tested positive so that would mean I should have been 6 weeks at the time of my drs visit. After blood work and sonograms I went back to the dr. Two weeks later and was 5 weeks pregnant. My husband I were so happy and then the same week I miscarried and suffered severe pain again


VAERS ID: 1855073 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: West Virginia  
Vaccinated:2021-04-16
Onset:2021-09-30
   Days after vaccination:167
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 028A21A / 2 RA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Synthroid, Albuterol inhaler
Current Illness: None
Preexisting Conditions: Thyroid disease, asthma
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Miscarriage


VAERS ID: 1798789 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-01
Onset:2021-09-30
   Days after vaccination:29
Submitted: 0000-00-00
Entered: 2021-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202101319209

Write-up: Abortion spontaneous; This is a spontaneous report from a contactable health professional via the Regulatory Authority. Regulatory authority report number is 636044. A 29-year-old pregnant female patient received bnt162b2 (COMIRNATY), via an unspecified route of administration on Sep2021 (lot number was not reported), dose number unknown, single for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. The patient experienced abortion spontaneous on 30Sep2021 with outcome of recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1799717 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-24
Onset:2021-09-30
   Days after vaccination:6
Submitted: 0000-00-00
Entered: 2021-10-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FE8087 / 1 LA / OT

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Headache, Liver function test, Lower respiratory tract infection, SARS-CoV-2 test
SMQs:, Termination of pregnancy and risk of abortion (narrow), Infective pneumonia (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: Heart disorder.
Allergies:
Diagnostic Lab Data: Test Date: 20211001; Test Name: LFT; Test Result: Negative; Test Date: 20211001; Test Name: nasal swab; Test Result: Negative.
CDC Split Type: GBPFIZER INC202101340001

Write-up: miscarriage; chest infection; headache; This is a spontaneous report from a contactable other health care professional. A 34-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Batch/Lot Number: FE8087), via intramuscular route, administered in left arm on 24Sep2021 as dose 1, single for COVID-19 immunisation. The patient was pregnant at the time of vaccination. Medical history included cardiac disorder. There were no concomitant medications. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medications within 2 weeks of vaccination. On 30Sep2021, the patient had miscarriage and experienced chest infection and headache. In general, the patient had a very healthy immune system after the vaccine the patient began to suffer from headaches then had a miscarriage and now had a chest infection. The mother reported she became pregnant while taking BNT162B2. The pregnancy resulted in spontaneous abortion. The fetal outcome was intrauterine death. The patient underwent lab tests and procedures which included liver function test: negative on 01Oct2021, SARS-COV-2 test: negative on 01Oct2021. The patient did not receive any treatment. The outcome was recovering for the reported events.


VAERS ID: 1852333 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-18
Onset:2021-09-30
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG7387 / 1 - / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Amenorrhea; Miscarriage; Obesity (BMI 29.4); Pregnancy loss $g20 weeks; Pregnancy normal (1 child born at term)
Allergies:
Diagnostic Lab Data: Test Name: SARS-CoV-2 test; Test Result: Negative
CDC Split Type: FRPFIZER INC202101436766

Write-up: Pregnancy loss <20 weeks gestation; This is a spontaneous report from a contactable physician downloaded from the regulatory authority-WEB, regulatory authority number FR-AFSSAPS-PA20211934. A 33-year-old female patient received bnt162b2 (COMIRNATY), dose 1 intramuscular on 18Sep2021 (Batch/Lot Number: FG7387) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included pregnancy loss $g20 weeks from 2019, obesity (BMI 29.4), pregnancy normal (1 child born at term), and miscarriage at 21 weeks of amenorrhea. The patient''s concomitant medications were not reported. On 30Sep2021, occurrence of Miscarriage < 20 weeks gestation. Pregnant at 16 weeks of amenorrhea at the moment of Dose 1: 2nd trimester spontaneous miscarriage. On (DATE UNKNOWN), SARS-CoV-2 Test: Negative. Clinical summary: miscarriage at 16 WA, at D + 12 of a D1 Comirnaty in a 33-year-old obese patient who had a miscarriage in 2019 at 21 WA. Miscarriage on 30Sep to 12 days after the comirnaty vaccine 1st dose. Pregnancy loss more than 20 weeks gestation. Time Interval between Beginning of Drug Administration and Start of Reaction / Event was 12 days. The outcome of event was Recovered/Resolved with Sequel. No follow-up attempts possible. No further information expected.


VAERS ID: 1765514 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-09-23
Onset:2021-10-01
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-10-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 212A21A / 1 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Back pain, Exposure during pregnancy, Haemorrhage, Muscle spasms, Pregnancy test positive, Ultrasound scan abnormal
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Retroperitoneal fibrosis (broad), Malignancy related therapeutic and diagnostic procedures (narrow), Dystonia (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), 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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamins
Current Illness: None
Preexisting Conditions: None
Allergies: Morphine and amoxicillin
Diagnostic Lab Data: I had a positive pregnancy test 09/29. On 10/4 the pregnancy test showed 2 HCG level and also an ultra sound showed no gestational sac. I had the miscarriage over the weekend.
CDC Split Type:

Write-up: I received the vaccine on 09/23/21. I started getting back pain and cramps 09/30-10/1, and started bleeding on 10/2-4. It was confirmed that I had a miscarriage.


VAERS ID: 1803844 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-09-30
Onset:2021-10-01
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-10-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 4 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamin and Folic acid supplement.
Current Illness: None
Preexisting Conditions: Asthma
Allergies: None
Diagnostic Lab Data: None.
CDC Split Type:

Write-up: I am not sure if it is directly related to the vaccine but I figured it was worth notifying as you can keep track and see if there is a trend or if my case was simply coincidental. I was 34 weeks pregnant when I received my first dose of Pfizer and the very next day, my water broke and I went into labor. Delivered a 34 week preemie. Again unsure if related or coincidence but I had no complications with my pregnancy so figured it was worth mentioning. Thank you.


VAERS ID: 1856762 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Missouri  
Vaccinated:2021-09-03
Onset:2021-10-01
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3184 / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CYMBALTA; FOLIC ACID; BARIATRIC ADVANTAGE ULTRA MULTI WITH IRON; ATIVAN; EMGALITY [GALCANEZUMAB]
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Depression; Polycystic ovarian syndrome; Pseudotumor cerebri; Sulfonamide allergy
Allergies:
Diagnostic Lab Data: Test Date: 202109; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative; Test Date: 20211025; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative
CDC Split Type: USPFIZER INC202101454411

Write-up: Miscarriage; This is a spontaneous report from a contactable other healthcare professional (patient). A 35-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 03Sep2021 (Batch/Lot Number: FC3184) (at the age of 35-years-old) as DOSE 2, SINGLE for COVID-19 immunisation. Medical history included sulfa allergy, polycystic ovarian syndrome (PCOS), pseudotumor cerebri, and depression; from unknown dates and unknown if ongoing. Patient was pregnant at time of vaccination, date of LMP was on 12Jun2021. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medications included duloxetine hydrochloride (CYMBALTA); folic acid; ascorbic acid, biotin, calcium pantothenate, camellia sinensis leaf, carotenoids nos, choline bitartrate, chromium picolinate, colecalciferol, copper citrate, ferrous fumarate, folic acid, inositol, magnesium glycinate, magnesium oxide, manganese citrate, mecobalamin, molybdenum aspartate, nicotinamide, phytomenadione, potassium bicarbonate, potassium iodide, punica granatum fruit, pyridoxine hydrochloride, retinol acetate, riboflavin, selenomethionine, thiamine hydrochloride, tocopheryl acid succinate, zinc glycinate (BARIATRIC ADVANTAGE ULTRA MULTI WITH IRON); lorazepam (ATIVAN); and galcanezumab (EMGALITY [GALCANEZUMAB]); all taken for unspecified indications, start and stop dates were not reported. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 09Aug2021 (Batch/Lot Number: FA7485) (at the age of 35-years-old) as DOSE 1, SINGLE for COVID-19 immunization. On 01Oct2021, the patient experienced miscarriage (medically significant).The mother was 16 Weeks pregnant at the onset of the event. The mother was due to deliver on an unknown date. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient been has been tested for COVID-19. The patient underwent lab tests and procedures which included nasal swab: negative in Sep2021, negative on 25Oct2021. The event resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of miscarriage which included dilation and curettage (D&C). The outcome of the event was recovered with sequelae.; Sender''s Comments: Based on the information available a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported events miscarriage. 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: 1845070 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-10-01
Onset:2021-10-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2834 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Nausea
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: NLPFIZER INC202101414933

Write-up: Miscarriage at 14 + 2 weeks; Nausea; This is a spontaneous report from a contactable consumer downloaded from the Regulatory Agency (RA)-WEB. The regulatory authority number is NL-LRB-00699822. A 37-year-old female patient received BNT162b2 (COMIRNATY), via an unspecified route of administration on 01Oct2021 (Batch/Lot Number: FF2834) as dose 1, single for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient had no previous COVID-19 infection. On 01Oct2021 (8 hours after start), the patient experienced nausea. On 03Oct2021 (also reported as 36 hours after start), the patient experienced miscarriage which occurred at a pregnancy duration of 14 + 2 weeks. The outcome of the event nausea was recovered on 02Oct2021, while for miscarriage was unknown. Sender Comment: Since the nature of the reported reaction does imply seriousness according to one of the agency criteria, the reaction was considered as serious by the Centre. Reporter''s Comments: Past drug therapy BioNTech/Pfizer vaccine (Comirnaty): no. Miscarriage. Additional information ADR: 14 weeks + 2 days of pregnancy. Confounding factors, vaccine exposure during pregnancy week: 14 weeks. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1757013 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2021-09-05
Onset:2021-10-02
   Days after vaccination:27
Submitted: 0000-00-00
Entered: 2021-10-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 3 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, 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? Yes
Recovered? No
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: None
Allergies: Ceclor, pediazol, rhondec DM
Diagnostic Lab Data: Ultrasound
CDC Split Type:

Write-up: Miscarriage occurred that same week


VAERS ID: 1758802 (history)  
Form: Version 2.0  
Age: 26.0  
Sex: Female  
Location: North Dakota  
Vaccinated:2021-09-30
Onset:2021-10-02
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-10-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (UNKNOWN)) / UNKNOWN MANUFACTURER - / 2 - / -

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Full blood count, Human chorionic gonadotropin, Maternal exposure before pregnancy, Metabolic function test, Ultrasound scan vagina, Urine analysis
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: No known allergies
Diagnostic Lab Data: In the ED on Sunday (10/3) I ran CBC, CMP, UA, Hcg, and sent her out for a transvaginal US.
CDC Split Type:

Write-up: Unknown brand of COVID vaccine as I did not order nor give it to the patient. May be correlation rather than causation as these things do happen, but patient had her second MRNA dose on Tuesday and reported miscarriage on Saturday. She did report some light spotting earlier that week prior to the miscarriage. Was seen in ED for abdominal pain and vaginal bleeding.


VAERS ID: 1768701 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-10-02
Onset:2021-10-02
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-10-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

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

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

Write-up: Z37.1 - Single stillbirth


VAERS ID: 1793744 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: California  
Vaccinated:2021-10-02
Onset:2021-10-02
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-10-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2589 / 3 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Chills, Delivery, Exposure during pregnancy, Foetal death, Foetal heart rate abnormal, Foetal hypokinesia, Full blood count, Headache, Hypersomnia, Pain in extremity, Stillbirth, Ultrasound foetal abnormal
SMQs:, Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Depression (excl suicide and self injury) (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow), 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? Yes, 3 days
   Extended hospital stay? No
Previous Vaccinations: chills headache, low grade fever and a sore arm
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: Penicilin
Diagnostic Lab Data: Dr ordered a full blood panel on October 4th when Pt was admitted into the hospital. An autopsy was ordered for the baby boy.
CDC Split Type:

Write-up: Pt was 26 weeks and 1 day pregnant when she got her 3rd Pfizer booster shot on Oct 2, 2021 at 2pm in the afternoon. After the injection on the left arm, she felt it become sore after 3 hours, and it worsened after 6 hours. On Oct 3rd, 2021 she had chills and a headache throughout the day and slept most of the day. On Oct 4th, 2021 she realized that she had not felt the baby kick and contacted her doctor. They told her to come into the hospital on Oct 4th 2021 and they determined that there was no long a heartbeat. Ultrasound showed that the baby likely died a day ago. Pt vaginally delivered the stillborn baby boy on Oct 5th, 2021. The baby was about 2 lbs.


VAERS ID: 1817692 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-10-02
Submitted: 0000-00-00
Entered: 2021-10-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Foetal death, Foetal hypokinesia, Maternal exposure during pregnancy, Rash pruritic
SMQs:, Anaphylactic reaction (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202101360776

Write-up: Maternal exposure during pregnancy; Foetal death; Foetal hypokinesia; Rash pruritic; This is a spontaneous report from a contactable other health professional via the Regulatory Authority. Regulatory authority report number is 639647. This other hcp reported information for both mother and fetus/baby. This is a maternal report. A 32-year-old female patient received BNT162B2 (COMIRNATY, solution for injection, Lot number was not reported), via an unspecified route of administration on an unspecified date as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Historically, the patient had received BNT162B2 (COMIRNATY, solution for injection, Lot number was not reported), via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. The mother reported she became pregnant while taking BNT162B2. On an unspecified date, the patient experienced maternal exposure during pregnancy. On 02Oct2021, the patient experienced foetal death, foetal hypokinesia and rash pruritic. Reportedly, the reactions experienced were foetal death, foetal hypokinesia and rash pruritic. The fetal outcome is intrauterine death. The outcome of the events foetal death, foetal hypokinesia and maternal exposure during pregnancy was unknown. The outcome of the event rash pruritic was recovered on an unspecified date in 2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1852769 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-10-02
Onset:2021-10-02
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG3739 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion, Gynaecological examination, Human chorionic gonadotropin, Maternal exposure during pregnancy, Uterine 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? 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: 20211012; Test Name: gynecological examination; Result Unstructured Data: Test Result:confiriming abortion; Test Date: 20211008; Test Name: betaHCG exam; Result Unstructured Data: Test Result:2100; Test Date: 20211011; Test Name: betaHCG exam; Result Unstructured Data: Test Result:250
CDC Split Type: ITPFIZER INC202101436848

Write-up: Fifth week abortion; start of bleeding from the uterus which will continue for all days to come; maternal exposure during pregnancy, first trimester; This is a spontaneous report from a contactable consumer or other non hcp, first of two cases. This is the first case which has been downloaded from the Agency WEB [IT-MINISAL02-800711]. This case was split to capture events that occurred after different doses. This is the first of two reports, for 2nd dose. A 43-years-old female patient received second dose of bnt162b2 (COMIRNATY, Formulation: Solution for injection, Batch/Lot Number: FG3739), via an unspecified route of administration on 02Oct2021 (at the age of 43-years-old) as dose 2, single for covid-19 immunisation. The medical history and concomitant medications were not reported. The patient received first dose of comirnaty on 11Sep2021 (lot FG3739) for covid-19 immunization and experienced Maternal exposure during pregnancy, first trimester. On 02Oct2021 the patient experienced maternal exposure during pregnancy, first trimester. On 03Oct2021 the patient experienced fifth week abortion and start of bleeding from the uterus which will continue for all days to come. The events fifth week abortion and start of bleeding from the uterus which will continue for all days to come were captured as serious (medically significant). The mother was 5 Weeks pregnant at the onset of the event. The pregnancy resulted in spontaneous abortion. The fetal outcome is intrauterine death. The patient underwent lab tests and procedures which included gynaecological examination: confiriming abortion on 12Oct2021, human chorionic gonadotropin: 2100 on 08Oct2021, human chorionic gonadotropin: 250 on 11Oct2021. The outcome of the event fifth week abortion was resolved with sequelae on 2021, for the event start of bleeding from the uterus which will continue for all days to come the outcome was unknown. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : IT-PFIZER INC-202101448606 same patient, 1/2 dose, different events


VAERS ID: 1774967 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Florida  
Vaccinated:2021-09-17
Onset:2021-10-03
   Days after vaccination:16
Submitted: 0000-00-00
Entered: 2021-10-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR

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

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

Write-up: At 5 weeks pregnant dose 1 was administered at 8 weeks a complete spontaneous miscarriage occurred


VAERS ID: 1807777 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: New York  
Vaccinated:2021-09-28
Onset:2021-10-03
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1822809 / 1 LA / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal Vitamin
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: I took a blood test to measure my hormone levels and had a sonogram that confirmed the miscarriage.
CDC Split Type:

Write-up: I took a positive pregnancy test on 9/17/21. This was my first pregnancy. I received the Janseen Vaccine 9/28 against my better judgement. I was mandated by the mayor. I started bleeding heavily on 10/3. I reported to the doctor 10/4 the baby was measuring 5 weeks with no heart beat. This was a week behind what I originally thought. I believed I should have been 6 weeks based on my menstrual cycle. I continued bleeding and cramping the whole week. I returned to the doctor 10/12 and the doctor confirmed I had miscarried. The doctor said it?s possible the baby stopped growing at 5 weeks ( which is when I received the vaccine).


VAERS ID: 1808054 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-10-01
Onset:2021-10-03
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FC3183 / 2 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Gynaecological examination, Haemorrhage, Human chorionic gonadotropin negative, Pregnancy
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: Went to OBYGYN on Monday the 4th and had my hcg levels tested and they declined from the week before significatly. Went back on the 6th to have more hcg levels checked and was told on the 8th that there was zero hcg in my system so I was no longer pregnant.
CDC Split Type:

Write-up: First pregnancy. Didn''t know I was pregnant when I received the first shot so marked no on the form. Informed the pharmacist of knowing I was pregnant and to change my form from the first shot but he said he didn''t have to. I had a miscarriage within 44 hours of receiving the shot. Bleeding.


VAERS ID: 1834888 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated:2021-10-03
Onset:2021-10-03
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG7900 / 2 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Dyspnoea, Foetal monitoring, Heart rate, Investigation, Maternal exposure during pregnancy, Pregnancy test, Premature delivery, Tachycardia foetal
SMQs:, Anaphylactic reaction (broad), Congenital and neonatal arrhythmias (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20211007; Test Name: Heart rate; Result Unstructured Data: Test Result:120-130; Comments: the normal trend of fetal heart rate was occurred through the whole night (in range 120-130 bpm).; Test Date: 20211008; Test Name: Heart rate; Result Unstructured Data: Test Result:240; Comments: the fetal heart rate revert to tachycardia (240 bpm).; Test Name: Fetus examination; Result Unstructured Data: Test Result:no anatomical and functional abnormalities; Comments: From the result of the physician''s examination so far there were no anatomical and functional abnormalities in the fetus''s heart. All was normal.; Test Name: Pregnancy test; Result Unstructured Data: Test Result:the fetus was normal and had no abnormalities; Comments: Pregnancy test before vaccination; Test Date: 20211004; Test Name: Fetomaternal checking; Result Unstructured Data: Test Result:no abnormalities identified; Comments: no abnormalities identified from fetal heart anatomy & function; Test Name: Heart rate; Result Unstructured Data: Test Result:Fetus heart rate did not decreased; Test Name: Heart rate; Result Unstructured Data: Test Result:Still tachycardia; Test Name: Heart rate; Result Unstructured Data: Test Result:120; Comments: Fetus''s heart rate could be normal at about 120 bpm but with help of the drug amiodarone; Test Name: Heart rate; Result Unstructured Data: Test Result:Above 220; Comments: Above 220 bpm; Test Name: Heart rate; Result Unstructured Data: Test Result:267; Comments: 267 bpm; Test Name: Heart rate; Result Unstructured Data: Test Result:110 - 120; Comments: the heart rate can be in normal range 110-120 bpm by periodic Amiodarone medication.; Test Date: 20211004; Test Name: Heart rate; Result Unstructured Data: Test Result:Above 220; Comments: Above 220 bpm. The physician diagnosed the baby with supraventricular tachycardia.
CDC Split Type: IDPFIZER INC202101462811

Write-up: Until finally the doctor decided that the fetus should be delivered at 33 weeks pregnancy.; the fetus''s heart rate did not decrease/the fetus''s heart rate was still tachycardia/diagnosed the baby with supraventricular tachycardia; The mother of fetus was vaccinated with condition of 30-weeks pregnancy; The baby also experienced short of breath, hence he needed the help of an oxygen tube to breathe; This is a spontaneous report from a contactable consumer on behalf of her fetus. This consumer reported information for both mother (herself) and fetus after dose 1 (one) and 2 (two) of vaccination. This is the fourth of four reports for a fetus report after dose 2 (two) of vaccination. This is a report combining information from duplicate reports 202101461700] and 202101462811]. The current and all subsequent follow-up information will be reported under manufacturer report number 202101462811. A fetus male patient received bnt162b2 (COMIRNATY), transplacental on 03Oct2021 (Batch/Lot Number: FG7900) as DOSE 2, SINGLE for covid-19 immunization. The patient''s medical history and concomitant medications were not reported. As per reported, the mother of fetus said that she was vaccinated against bnt162b2 vaccine and she did not experience any Adverse Event Following Immunization (AEFI), but her fetus condition had changed after vaccination. However, she did not know for sure whether the change in her fetus was caused by AEFI or not. The mother of fetus was vaccinated with condition of 30-weeks pregnancy on an unspecified date with an outcome of not recovered. At the time of pregnancy test before vaccination, the fetus was normal and had no abnormalities. Then 20 days after the first vaccination, fetus''s heart rate had tachycardia (above 220 bpm). A day after, the mother of fetus still got her second vaccination (21 days after the first vaccination). Then the mother of fetus was referred to a hospital because the fetus''s heart rate did not decrease on an unspecified date with outcome of not recovered. Until finally the physician decided that the fetus should be delivered at 33 weeks pregnancy on an unspecified date with outcome of unknown. 2 (two) weeks since the c-section operation until the time of reporting, the fetus''s heart rate was still tachycardia on an unspecified date with outcome of not recovered, and it could be normal at about 120 bpm but with help of the drug amiodarone (AMIODARONE). From the result of the physician''s examination so far there were no anatomical and functional abnormalities in the fetus''s heart. All was normal. However, only the fetus''s heart rate was above 220 bpm (once it has reached 267 bpm). The mother of fetus was routinely taking a test for her pregnancy and did not find any abnormalities until after the vaccination. The patient underwent lab tests and procedures which included heart rate: fetus heart rate did not decreased on unspecified date, heart rate: still tachycardia on unspecified date, heart rate: Fetus''s heart rate could be normal at about 120 bpm on unspecified date but with help of the drug amiodarone, heart rate: Above 220 bpm on unspecified date, heart rate: 267 bpm on unspecified date, investigation: From the result of the physician''s examination so far there were no anatomical and functional abnormalities in the fetus''s heart on unspecified date. All was normal, pregnancy test: the fetus was normal and had no abnormalities at the time of pregnancy test before vaccination. Therapeutic measures were taken as a result of the fetus''s heart rate did not decrease/2 (two) weeks since the c-section operation until the time of reporting, the fetus''s heart rate was still tachycardia (tachycardia foetal). As per reported, the mother of fetus got her second dose of Pfizer covid-19 vaccine on 03Oct2021 with Pfizer lot number FG7900. Then on 04Oct2021, the mother of fetus got the fetomaternal checking with the result no abnormalities identified from fetal heart anatomy and function, but still, the fetal heart rate was above 220 bpm. Her doctor diagnosed her baby with supraventricular tachycardia. The fetomaternal subspecialist recommended the mother of fetus to get hospitalized to monitor her fetal heart rate (since this was a rare case and the therapy will be considered by cross-specialist doctor). On 06Oct2021, the mother of fetus started to be hospitalized, the doctor already planned to have digoxin (DIGOXIN) injection through the fetal umbilical cord on 07Oct2021 (really the first time therapy doing in Indonesia for fetal tachycardia). On 07Oct2021 after digoxin injection through umbilical cord, the normal trend of fetal heart rate was occurred through the whole night (in range 120-130 bpm). On 08Oct2021 morning, the fetal heart rate reverted to tachycardia (240 bpm). Another plan was made by Doctors to have amiodarone injection through umbilical cord as well, executed on 12Oct2021. No response on fetal heart rate after amiodarone injection. Final decision by Doctor team was to give birth of the baby at 32-33 weeks at that time. On 14Oct2021, the baby was born through C-section operation process. After that day until the time of reporting (27Oct2021), the baby was still monitored in Neonatal Intensive Care Unit (NICU) with tachycardia condition, the heart rate could be in normal range 110-120 bpm by periodic amiodarone medication. It was also informed that the baby was a boy. The mother of fetus informed that when her baby experienced tachycardia which was the heart rate was very fast, the baby also experienced short of breath on an unspecified date with an outcome of recovered, hence he needed the help of an oxygen tube to breathe. Currently as it has been controlled with administration of amiodarone, the baby did not use the oxygen tube anymore. According to the doctor''s examination, there were no anatomical and functional abnormalities in the baby''s heart. The patient was hospitalized for the event The mother of fetus was vaccinated with condition of 30-weeks pregnancy and the fetus''s heart rate did not decrease/2 (two) weeks since the c-section operation until the time of reporting, the fetus''s heart rate was still tachycardia/the physician diagnosed the baby with supraventricular tachycardia from 06Oct2021 to an unknown date and was hospitalized from an unspecified date for the event Until finally the doctor decided that the fetus should be delivered at 33 weeks pregnancy. The patient underwent lab tests and procedures which included Fetomaternal checking (foetal monitoring): no abnormalities identified on 04Oct2021 (no abnormalities identified from fetal heart anatomy & function), heart rates: fetus heart rate did not decreased on an unspecified date, still tachycardia on an unspecified date, 120 on an unspecified date (Fetus''s heart rate could be normal at about 120 bpm but with help of the drug amiodarone), above 220 on on an unspecified date (Above 220 bpm), 267 on an unspecified date (267 bpm), 110 - 120 on an unspecified date (the heart rate can be in normal range 110-120 bpm by periodic Amiodarone medication), above 220 on 04Oct2021 -Above 220 bpm. The physician diagnosed the baby with supraventricular tachycardia, 120-130 on 07Oct2021 - the normal trend of fetal heart rate was occurred through the whole night (in range 120-130 bpm), 240 on 08Oct2021 -the fetal heart rate revert to tachycardia (240 bpm), Fetus examination (investigation): no anatomical and functional abnormalities on an unspecified date (From the result of the physician''s examination so far there were no anatomical and functional abnormalities in the fetus''s heart. All was normal, pregnancy test: the fetus was normal and had no abnormalities on an unspecified date (Pregnancy test before vaccination). Therapeutic measures were taken as a result of the fetus''s heart rate did not decrease/2 (two) weeks since the c-section operation until the time of reporting, the fetus''s heart rate was still tachycardia/the physician diagnosed the baby with supraventricular tachycardia and the baby also experienced short of breath, hence he needed the help of an oxygen tube to breathe. The outcome of the event The mother of fetus was vaccinated with condition of 30-weeks pregnancy and the fetus''s heart rate did not decrease/2 (two) weeks since the c-section operation until the time of reporting, the fetus''s heart rate was still tachycardia/The physician diagnosed the baby with supraventricular tachycardia was not recovered. Outcome of the event Until finally the doctor decided that the fetus should be delivered at 33 weeks pregnancy was unknown. Outcome of The baby also experienced short of breath, hence he needed the help of an oxygen tube to breathe was recovered.; Sender''s Comments: Linked Report(s) : ID-PFIZER INC-202101460743 Maternal case (2nd dose of vaccination);ID-PFIZER INC-202101454978 Same reporter, suspect product; Different patient and event


VAERS ID: 1850722 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: California  
Vaccinated:2021-09-23
Onset:2021-10-04
   Days after vaccination:11
Submitted: 0000-00-00
Entered: 2021-11-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 211A21A / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Amniocentesis, Chromosome analysis normal, Exposure during pregnancy, Foetal death, Ultrasound antenatal screen abnormal, Uterine dilation and curettage
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal multi-vitamin Prenatal folic acid Prenatal DHA
Current Illness: None
Preexisting Conditions: Mild asthma
Allergies: None
Diagnostic Lab Data: 10/18/21: routine check up - no heartbeat detected through Doppler and ultrasound showed no signs of life 10/18/21 - 10/19/21: radiology confirmation of status of fetus - confirmed fetal demise 10/22/21: post-mortem amniocentesis diagnostic procedure performed by Dr. 10/26/21: part 1 of 2 Dilation and Evacuation surgery procedure performed by Dr. 10/27/21: part 2 of 2 Dilation and Evacuation surgery procedure performed by Dr. 11/03/21: received results of amniocentesis by Dr. - no chromosomal issues detected in amniotic fluid 11/03/21: received results of pathology analysis by Dr. - no abnormalities detected in fetus
CDC Split Type:

Write-up: Miscarriage at 13-14 weeks gestation. Estimated due date: 4/12/22. Previous ultrasounds showed baby in good health prior to vaccine. NIPT and nuchal translucenscy tests were negative for chromosomal abnormalities. A post-mortem amniocentesis and pathology analysis showed no chromosomal or pathological defects. 1 previous pregnancy: vaginal delivery of healthy baby on 2/6/2018 by same provider. Baby weighed 7 lbs, 9oz


VAERS ID: 1817677 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-10-04
Submitted: 0000-00-00
Entered: 2021-10-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202101360704

Write-up: Abortion spontaneous; This is a spontaneous report from a contactable other health professional via the Regulatory Authority. Regulatory authority report number is 636852. A 43-year-old female patient received BNT162B2 (COMIRNATY, Solution for injection, Lot number was not reported), via an unspecified route of administration on an unspecified date as DOSE NUMBER UNKNOWN, SINGLE for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. The patient experienced abortion spontaneous on 04Oct2021. The outcome of the event was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1830194 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-10-04
Onset:2021-10-04
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-10-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness: Breast feeding
Preexisting Conditions: Medical History/Concurrent Conditions: Multigravida
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC202101393060

Write-up: Miscarriage; ongoing breastfeeding; ongoing breastfeeding; This is a spontaneous report from a contactable consumer (patient). This is a report received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202110161453401460-77IZ6, Safety Report Unique Identifier GB-MHRA-ADR 26084921. This consumer reported information for both mother and fetus/child. This is the maternal report. A 39-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number and Expiration date was unknown), via an unspecified route of administration on 04Oct2021 (at the age of 39 years old) as dose 3 (booster), single for COVID-19 immunisation. Medical history included ongoing breast feeding and previously had 3 healthy pregnancies. Concomitant medication included folic acid taken for folic acid supplementation. The reporter stated that it was probably unrelated but for data collection, the patient received the COVID booster vaccine. When approximately 7 weeks pregnant, prior to receiving the vaccine, fetal heartbeat was detected. She subsequently had a miscarriage the following week on 13Oct2021. The mother reported she became pregnant while taking bnt162b2. Patient was exposed to the medicine first-trimester (1-12 weeks). The pregnancy resulted in spontaneous abortion. The fetal outcome is congenital anomaly. Patient has not tested positive for COVID-19 since having the vaccine. Patient is not enrolled in clinical trial. Outcome of the miscarriage was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Sender''s Comments: based on the known safety profile of vaccine and the information available the event spontaneous abortion was considered as unrelated to the suspect drug.


VAERS ID: 1764793 (history)  
Form: Version 2.0  
Age: 23.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-06-07
Onset:2021-10-05
   Days after vaccination:120
Submitted: 0000-00-00
Entered: 2021-10-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 01A8823 / 1 RA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 01A2163 / 1 RA / SYR

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

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

Write-up: 2 Miscarriage''s directly following vaccine. Had two pregnancies beforehand with no complications to the baby or mother. Mother in perfect healthy condition.


VAERS ID: 1836306 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-10-05
Submitted: 0000-00-00
Entered: 2021-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202101402279

Write-up: Stillbirth; This is a spontaneous report from a contactable other health professional via the Regulatory Authority. Regulatory authority report number is 641850. A 32-year-old female patient received BNT162B2 (COMIRNATY, mRNA vaccine, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunization. The patient medical history and concomitant medications were not reported. On 05Oct2021 stillbirth was reported. The outcome of the event was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1847142 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-10-03
Onset:2021-10-05
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / OT

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

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

Write-up: Abortion spontaneous; This case was received via regulatory authority (Reference number: EE-SAM-545521100728) on 29-Oct-2021 and was forwarded to Moderna on 29-Oct-2021. This regulatory authority retrospective pregnancy case was reported by a consumer and describes the occurrence of ABORTION SPONTANEOUS (Abortion spontaneous) in a 25-year-old female patient (gravida 1) who received mRNA-1273 (Spikevax) for Active immunization. The patient''s past medical history included Delivery on 21-Jan-2021. On 03-Oct-2021, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) .5 milliliter. The patient''s last menstrual period was on 19-Aug-2021 and the estimated date of delivery was 26-May-2022. On 05-Oct-2021, after starting mRNA-1273 (Spikevax), the patient experienced ABORTION SPONTANEOUS (Abortion spontaneous) (seriousness criterion medically significant). The patient received mRNA-1273 (Spikevax) beginning around the seventh week of the pregnancy. The delivery occurred on 06-Oct-2021, which was reported as Spontaneous Abortion. For foetus 1, The outcome was reported as Spontaneous Abortion NOS. On 06-Oct-2021, ABORTION SPONTANEOUS (Abortion spontaneous) had resolved. No concomitant medications were provided by the reporter. No treatment information was provided by the reporter. It was reported as possible coincidence, abortions occur regardless of vaccination. This is a regulatory pregnancy case concerning a 25-year-old female patient with no reported medical history, who experienced the serious unexpected event Abortion spontaneous. Patient received the first dose mRNA-1273 (Spikevax) at 6 weeks of gestation, and event occurred 3 days after. The benefit-risk relationship of mRNA-1273 Moderna vaccine is not affected by this report.; Reporter''s Comments: Possible coincidence, abortions occur regardless of vaccination.; Sender''s Comments: This is a regulatory pregnancy case concerning a 25-year-old female patient with no reported medical history, who experienced the serious unexpected event Abortion spontaneous. Patient received the first dose mRNA-1273 (Spikevax) at 6 weeks of gestation, and event occurred 3 days after. The benefit-risk relationship of mRNA-1273 Moderna vaccine is not affected by this report.


VAERS ID: 1768977 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Florida  
Vaccinated:2021-08-02
Onset:2021-10-07
   Days after vaccination:66
Submitted: 0000-00-00
Entered: 2021-10-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / -

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

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

Write-up: Miscarriage at 10 weeks


VAERS ID: 1793977 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-09-27
Onset:2021-10-07
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-10-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / IM

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

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 14 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: NA
Current Illness: NA
Preexisting Conditions: NA
Allergies: NKA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Ruptured membrane occurred at 6:30PM on 07OCT2021. Labor began around 9:00PM on 07OCT2021. Premature baby born at 6:38AM on 08OCT2021 at 34 weeks and 4 days. Original due date was 15NOV 2021. Premature baby admitted to NICU for undetermined length of stay to promote growth. Mother discharged 48 hours following delivery.


VAERS ID: 1795999 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: New York  
Vaccinated:2021-10-04
Onset:2021-10-07
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-10-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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: 10/18 sonogram
CDC Split Type:

Write-up: Miscarriage - no fetal heartbeat after confirmed pregnancy and hormone levels measured


VAERS ID: 1837071 (history)  
Form: Version 2.0  
Age: 24.0  
Sex: Female  
Location: Kansas  
Vaccinated:2021-09-17
Onset:2021-10-07
   Days after vaccination:20
Submitted: 0000-00-00
Entered: 2021-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test abnormal, Exposure during pregnancy, Human chorionic gonadotropin negative
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: Daily prenatal
Current Illness: None
Preexisting Conditions: None
Allergies: No known allergies
Diagnostic Lab Data: Hcg drawn 10/5 and 10/7.
CDC Split Type:

Write-up: Miscarriage after receiving 2nd Covid vaccine during first trimester, confirmed at doctors office by bloodwork. Estimated due date June 1, 2022.


VAERS ID: 1849328 (history)  
Form: Version 2.0  
Age: 22.0  
Sex: Female  
Location: Hawaii  
Vaccinated:2021-09-08
Onset:2021-10-07
   Days after vaccination:29
Submitted: 0000-00-00
Entered: 2021-11-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / SYR

Administered by: Military       Purchased by: ?
Symptoms: Abortion spontaneous, Coagulopathy, Exposure during pregnancy, Lymphocyte percentage decreased, Neutrophil percentage increased, Platelet count increased, Red cell distribution width increased
SMQs:, Haematopoietic leukopenia (broad), Haemorrhage laboratory terms (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: Strawberries
Diagnostic Lab Data: RDW CV - 16.9% high oct.28.21 RDW - 17.2% high oct.20.21 Platelets - 466.0 x 10^9L high Oct.20.21 Neutrophil % auto - 79.3 high oct.28.21 Lymphocytes- 20% low oct.20 -16% low oct.28th
CDC Split Type:

Write-up: Blood clotting. I was pregnant the day I got the first vaccine, my due date was 5/27/22. The blood clotting caused a miscarriage on October 28th 2021.


VAERS ID: 1798138 (history)  
Form: Version 2.0  
Age: 38.0  
Sex: Female  
Location: New York  
Vaccinated:2021-10-05
Onset:2021-10-08
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-10-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous incomplete, Blood test normal, Condition aggravated, Heavy menstrual bleeding, Thrombosis, Ultrasound uterus abnormal, Uterine dilation and curettage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Thrombophlebitis (broad), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Colace, eye drops
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Ultrasound showed incomplete miscarriage, blood tests were normal
CDC Split Type:

Write-up: Completely unsure if related at all to the vaccine, but 3 days after my third dose of Pfizer I had very very severe menstrual bleeding. Turns out a miscarriage from Aug 5, 2021 was not 100% "complete" and this was my first period since pre-pregnancy. The bleeding was so sudden and SO severe (massive blood clots) that I went to the ER. The bleeding slowed down after 2-3 hours, but I had to have a D&C later that day. The only reason I''m reporting it is because it had been 2 full months since the miscarriage and my body did not have a reaction to the incomplete miscarriage -- but was there something about getting the vaccine that triggered this kind of severe bleeding/response to the remnants of the pregnancy?


VAERS ID: 1814355 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Georgia  
Vaccinated:2021-10-01
Onset:2021-10-08
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 301358A / 1 LA / SYR

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

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

Write-up: Site: Pain at Injection Site-Mild, Systemic: patient had a miscarriage-Severe, Additional Details: patient had a miscarriage


VAERS ID: 1849343 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Wisconsin  
Vaccinated:2021-10-06
Onset:2021-10-08
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-11-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Extra dose administered, Full blood count, Human chorionic gonadotropin, Metabolic function test, Ultrasound scan
SMQs:, Termination of pregnancy and risk of abortion (narrow), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal vitamin
Current Illness: None
Preexisting Conditions: None
Allergies: Sulfa medications Shellfish
Diagnostic Lab Data: Ultrasounds, CBC, BMP, beta HCG
CDC Split Type:

Write-up: Received booster dose of Pfizer COVID vaccine on 10/6/2021, which is approximately the same time my pregnancy stopped progressing and resulted in a miscarriage. I was 5 weeks 5 days pregnant at the time of vaccination, and on 10/29/21 at an ultrasound it was determined the fetus stopped developing around 6 weeks gestation. I miscarried the pregnancy on 11/3/21.


VAERS ID: 1816390 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-10-08
Onset:2021-10-08
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-10-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NICORETTE
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnant
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC202101359465

Write-up: miscarriage; This is a spontaneous report from a contactable physician received from The regulatory authority report number is GB-MHRA-TPP37207706C5448553YC1633691217165, and Safety Report Unique Identifier is GB-MHRA-ADR 26050897. A 35-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (batch/lot number not reported), via an unspecified route of administration on 08Oct2021 (at the age of 35 years old) as dose number unknown, single for COVID-19 immunisation. Medical history included pregnancy from an unknown date and unknown if ongoing. Concomitant medication included nicotine (NICORETTE) taken for an unspecified indication from 18Aug2021. The patient experienced miscarriage on 08Oct2021 with outcome of unknown. Miscarried a few weeks after jab at 12 weeks gestation - probably not related but notified as new vaccine. The event was reported serious as other medically important condition. No follow-up attempts are possible; information about batch/lot number cannot be obtained. No further information is expected.


VAERS ID: 1826107 (history)  
Form: Version 2.0  
Age: 0.08  
Sex: Unknown  
Location: Foreign  
Vaccinated:2021-10-08
Onset:2021-10-08
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-10-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Foetal death, 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? Yes
   Date died: 2021-10-01
   Days after onset: 7
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAPFIZER INC202101440061

Write-up: tThis is a spontaneous report from a contactable consumer (patient''s mother) received. This consumer reported events for both the mother and the baby. This is the baby (fetus) case. A 6-weeks-old patient of unspecified gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via transplacental on 08Oct2021 at 18:00 (Batch/Lot number was not reported) as dose 1, single for Covid-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient''s mother was around 6 weeks pregnant by the time she received the first shot on 08Oct2021, and she was told that it will not affect the baby, but it goes the other way; the heartbeat of the baby stopped on the same day she received the Pfizer Covid 19 shot and after a couple of days, she started bleeding a lot which caused miscarriage. No treatment was administered for the events. The patient died in Oct2021. It was unknown if an autopsy was performed. The lot number for BNT162B2 was not provided and will be requested during follow up.; Sender''s Comments: Linked Report(s) : CA-PFIZER INC-202101428452 Maternal report; Reported Cause(s) of Death: the heartbeat of the baby stoped; Maternal exposure during pregnancy, first trimester


VAERS ID: 1846713 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-10-08
Onset:2021-10-08
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-11-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Foetal death
SMQs:, 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? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAPFIZER INC202101428452

Write-up: the heartbeat of the baby stopped; started bleeding a lot which caused miscarriage; This is a spontaneous report from a contactable consumer (patient). This consumer reported information for both mother and fetus/baby. This is the maternal report. A 37-year-old pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration, administered in left arm on 08Oct2021 at 18:00 (Batch/Lot number was not reported) (at the age of 37-years-old) as dose 1, single for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient was pregnant at time of vaccination. Vaccination facility type was a regulatory authority. The patient''s last menstrual date was on 09Aug2021. The expected delivery or due date was on 23May2022. The patient''s gestational period when reaction/event was observed in the fetus was 6 weeks. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and did not receive other medications within 2 weeks of vaccination. On 08Oct2021 at 18:00, the patient reported that she was around 6weeks in pregnancy by the time she took the first shot and they told her it will not affect her baby, but it went the other way; the heartbeat of the baby stopped the same day she took the Pfizer and after a couple of days she started bleeding a lot which caused miscarriage. The event resulted to a visit in the Emergency room and doctor''s office/clinic visit. The patient was not diagnosed with COVID-19 prior to vaccination and has not been tested for COVID-19 since the vaccination. The patient did not receive treatment. The outcome of the event heartbeat of the baby stopped was fatal, while for miscarriage was recovering/resolving. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : CA-PFIZER INC-202101440061 baby (fetus) case


VAERS ID: 1818400 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Maryland  
Vaccinated:2021-09-28
Onset:2021-10-09
   Days after vaccination:11
Submitted: 0000-00-00
Entered: 2021-10-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 RA / SYR

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

Write-up: I was 6 weeks pregnant at the time and suffered from a miscarriage 2 weeks later after receiving 1st dose in 1st trimester. 2 weeks after shot I should have been 8 weeks and baby was only measuring 6 weeks with no heartbeat. The timing adds up perfectly from 1st dose when baby stopped growing to complete miscarriage. The vaccine killed my baby. Should not be given in 1st trimester, the most important trimester.


VAERS ID: 1834374 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-13
Onset:2021-10-09
   Days after vaccination:26
Submitted: 0000-00-00
Entered: 2021-11-01
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion late
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: C-section
Allergies:
Diagnostic Lab Data:
CDC Split Type: ESPFIZER INC202101390941

Write-up: ABORTION according to 15 weeks; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority-WEB, regulatory authority number ES-AEMPS-1025938. A 36-years-old female patient received bnt162b2 (COMIRNATY), via an unspecified route of administration on 13Sep2021 (Batch/Lot Number: Unknown) as dose 2, single for COVID-19 immunisation. Medical history included C-section from an unknown date and unknown if ongoing. The patient''s concomitant medications were not reported. The patient previously received first dose of bnt162b2 (COMIRNATY) via intramuscular on 23Aug2021 (batch/lot number unknown) for COVID-19 immunisation. The patient experienced abortion according to 15 weeks on 09Oct2021. The outcome of the event was recovered on 10Oct2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1836272 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:2021-10-09
Submitted: 0000-00-00
Entered: 2021-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Foetal death, Maternal exposure during pregnancy, Polyhydramnios
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? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: AUPFIZER INC202101402019

Write-up: Maternal exposure during pregnancy; Foetal death; Polyhydramnios; This is a spontaneous report received from a contactable other health professional via the Agency Regulatory Authority. Regulatory authority report number is 642769. This other hcp reported information for both mother and fetus/baby. A 28-year-old female patient received second dose of bnt162b2 (COMIRNATY, solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on an unspecified date as dose 2, single and received first dose via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced foetal death, polyhydramnios on 09Oct2021and maternal exposure during pregnancy on an unspecified date. The mother reported she became pregnant while taking bnt162b2. The fetal outcome is intrauterine death. Outcome of all events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1838038 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-10-09
Onset:2021-10-09
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Hypokinesia, Maternal exposure during pregnancy, Myalgia, Pain in extremity, SARS-CoV-2 test
SMQs:, Rhabdomyolysis/myopathy (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Eosinophilic pneumonia (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Hypotonic-hyporesponsive episode (broad), Tendinopathies and ligament disorders (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: FOLIC ACID
Current Illness: Pregnancy
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid supplementation; Miscarriage; Suspected COVID-19 (Unsure when symptoms stopped)
Allergies:
Diagnostic Lab Data: Test Name: blood work; Result Unstructured Data: Test Result:came back NAD; Comments: All routine blood work for 28week pregnancy came back NAD; Test Date: 20201010; Test Name: COVID-19 virus test; Test Result: Positive ; Comments: Yes - Positive COVID-19 test
CDC Split Type: GBPFIZER INC202101400779

Write-up: muscle pain; cannot raise arm; Painful arm; Maternal exposure during pregnancy, Second-trimester; miscarriages; This is a spontaneous report from a contactable consumer (patient). This is a report received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-APPCOVID-20211017111620 Safety Report Unique Identifier GB-MHRA-ADR 26085365. This is a maternal report. A 35-years-old (2 trimester pregnant) female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot: not reported) via an unspecified route of administration on 09Oct2021 (at the age of 35-years-old) as dose number unknown, single for COVID-19 immunisation. Medical history included ongoing pregnancy and suspected COVID-19 from 09Oct2020 (unsure when symptoms stopped), folic acid supplementation and consecutive miscarriages (prescribed folic acid due to 3 consecutive miscarriages prior to this pregnancy). Concomitant medication included folic acid as folic acid supplementation, start and stop date were not reported. Patient was not currently breastfeeding. Patient was not enrolled in clinical trial. On 09Oct2021, patient had maternal exposure during pregnancy, second trimester. On 10Oct2021 (after 1 day of vaccination), patient experienced painful arm. On 14Oct2021 (after 5 days of vaccination), patient experienced muscle pain and cannot raise arm. On an unspecified date, patient had miscarriage. Events were medically significant. Arm painful to touch/ lie on from 10Oct2021 or 11Oct2021. Seemed to resolve but muscle pain gradually got worse from 14Oct2201 until eventually patient now cannot raise arm, paracetamol taken but no relief given at all. Pain still getting worse as of today 17Oct2021. The mother reported she became pregnant while taking bnt162b2. Therapeutic measures were taken as a result of muscle pain, cannot raise arm and painful arm. The patient underwent lab tests and procedures which included COVID-19 virus test: positive on 10Oct2020 and on an unspecified date, all routine blood work for 28week pregnancy came back NAD. The outcome of event muscle pain, miscarriage was resolving, maternal exposure during pregnancy, second trimester was unknown, painful arm was not resolved and cannot raise arm was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 1841653 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-28
Onset:2021-10-09
   Days after vaccination:11
Submitted: 0000-00-00
Entered: 2021-11-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Foetal 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? 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: Steroid therapy (Taking regular steroid treatment (e.g. orally or rectally))
Allergies:
Diagnostic Lab Data: Test Date: 20211012; Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: Negative
CDC Split Type: GBMODERNATX, INC.MOD20213

Write-up: Fetal exposure during pregnancy; Early miscarriage; This case was received via Regulatory Authority (Reference number: GB-MHRA-ADR 26120532) on 26-Oct-2021 and was forwarded to Moderna on 26-Oct-2021. This regulatory authority retrospective pregnancy case was reported by a consumer and describes the occurrence of ABORTION SPONTANEOUS (Early miscarriage) in a 35-year-old female patient who received mRNA-1273 (Moderna CoviD-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included Steroid therapy (Taking regular steroid treatment (e.g. orally or rectally)). Concomitant products included FOLIC ACID for Folic acid supplementation. On 28-Sep-2021, the patient received first dose of mRNA-1273 (Moderna CoviD-19 Vaccine) (Transplacental) 1 dosage form. The patient''s last menstrual period was on 27-Aug-2021 and the estimated date of delivery was 03-Jun-2022. IN Oct2021, the patient experienced ABORTION SPONTANEOUS (Early miscarriage) (seriousness criterion medically significant). On an unknown date, the patient experienced FETAL EXPOSURE DURING PREGNANCY (Fetal exposure during pregnancy). The patient received mRNA-1273 (Moderna CoviD-19 Vaccine) beginning around the fourth week of the pregnancy. The delivery occurred on an unknown date, which was reported as Spontaneous Abortion. For fetal 1, The outcome was reported as Spontaneous Abortion NOS. At the time of the report, ABORTION SPONTANEOUS (Early miscarriage) had not resolved and FETAL EXPOSURE DURING PREGNANCY (Fetal exposure during pregnancy) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 12-Oct-2021, SARS-CoV-2 test: no - negative covid-19 test (Negative) Negative. The action taken with mRNA-1273 (Moderna CoviD-19 Vaccine) (Transplacental) was unknown. No treatment was provided. This is a case of Fetal Exposure During Pregnancy concerning a 35-year-old, female patient with no relevant medical history, who experienced the unexpected event of Abortion Spontaenous. The patient received the first dose of vaccine at 4 weeks of gestation. Spontaneous abortion occurred approximately 11 days after the first dose of mRNA-1273 (Moderna COVID-19 Vaccine). The benefit-risk relationship of mRNA-1273 (Moderna COVID-19 Vaccine) is not affected by this report.; Sender''s Comments: This is a case of Fetal Exposure During Pregnancy concerning a 35-year-old, female patient with no relevant medical history, who experienced the unexpected event of Abortion Spontaenous. The patient received the first dose of vaccine at 4 weeks of gestation. Spontaneous abortion occurred approximately 11 days after the first dose of mRNA-1273 (Moderna COVID-19 Vaccine). The benefit-risk relationship of mRNA-1273 (Moderna COVID-19 Vaccine) is not affected by this report.


VAERS ID: 1853606 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-10-09
Onset:2021-10-10
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-11-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30155BA / 3 RA / IM

Administered by: Work       Purchased by: ?
Symptoms: Abortion spontaneous, Extra dose administered, Foetal heart rate abnormal, Uterine dilation and curettage, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Medication errors (narrow)

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

Write-up: Post 3rd vaccination, I began bleeding vaginally on 10/10. The bleeding continued for 12 days then subsided for several days and returned. Ultrasound revealed a low fetal heart rate on 10/25. On 11/2 there was no longer a fetal heartbeat showing miscarriage. A D&C followed on 11/6.


VAERS ID: 1838022 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-07
Onset:2021-10-10
   Days after vaccination:33
Submitted: 0000-00-00
Entered: 2021-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FG9428 / 1 LA / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210905; Test Name: Sars-Cov-2 test; Test Result: Negative
CDC Split Type: FRPFIZER INC202101395011

Write-up: Miscarriage; This is a spontaneous report from a contactable consumer downloaded from the Regulatory Agency (RA)-WEB, regulatory authority number FR-AFSSAPS-TO20218449. A 30-year-old female patient received bnt162b2 (COMIRNATY), dose 1 intramuscular, administered in Arm Left on 07Sep2021 (Batch/Lot Number: FG9428) as dose 1, single for Covid-19 immunization. The patient''s medical history and concomitant medications were not reported. The patient was 1 Trimester pregnant at the onset of the event. The pregnancy resulted in spontaneous abortion. On 10Oct2021, she presented a spontaneous miscarriage. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 05Sep2021. The outcome of event was recovered with sequalae on 10Oct2021. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1847910 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-07-25
Onset:2021-10-12
   Days after vaccination:79
Submitted: 0000-00-00
Entered: 2021-11-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? 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 INC202101463260

Write-up: a few months after the second vaccination I had a miscarriage; I had a miscarriage, 12Oct. 5th week of pregnancy; This is a spontaneous report from a contactable consumer or other non-HCP (patient) downloaded from the WEB NL-LRB-00700975, Safety Report Unique Identifier NL-LRB-00703833. A 36-year-old female patient received second dose of bnt162b2 (COMIRNATY, Solution for injection, Lot Number and Expiry Date: not reported) via an unspecified route of administration on 25Jul2021 as DOSE 2, SINGLE for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. Historical vaccine included first dose of bnt162b2 (COMIRNATY, Solution for injection, Lot Number and Expiry Date: not reported) via an unspecified route of administration on 20Jun2021 as DOSE 1, SINGLE for COVID-19 immunization. The patient not had previous COVID infection. On 12Oct2021, the patient experienced a miscarriage, 5th week of pregnancy. Maternal exposure during pregnancy following administration of covid-19 vaccine pfizer injvlst and on an unspecified date, experienced a few months after the second vaccination she had a miscarriage. The COVID vaccinations took place before pregnancy. Reported stop date for event miscarriage on 19Oct2021. Outcome of events was unknown. Reporter Comment: Since the nature of the reported reaction does imply seriousness according to one of the CIOMS criteria, the reaction (miscarriage) was considered as serious by the regulatory authority. No follow-up attempts are possible. Information on batch/lot number cannot be obtained. No further information expected.


VAERS ID: 1795560 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Nebraska  
Vaccinated:2021-10-12
Onset:2021-10-13
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-10-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Arrhythmia, Blood test, Chest discomfort, Chest pain, Electrocardiogram, Exposure during pregnancy, Palpitations
SMQs:, Anaphylactic reaction (broad), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Cardiac arrhythmia terms, nonspecific (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zyrtec 4 tablets daily, Montelukast 1 tablet daily, Prednisone as needed
Current Illness: None
Preexisting Conditions: Idiopathic angioedema
Allergies: None
Diagnostic Lab Data: Blood test to confirm miscarriage was completed on 10/15/2021. EKG completed on 10/18/2021. Echocardiogram was ordered for 10/19/2021 for further testing of heart condition.
CDC Split Type:

Write-up: 1st dose of Moderna Covid-19 vaccine was received 09/14/2021. Abnormal heart rhythm with palpitations began on 10/5/21. Symptoms returned intermittently for one week. Second dose of Moderna Covid-19 Vaccine was received on 10/12/2021. Abnormal heart rhythm, palpitations, chest pain and tightness returned on 10/13/21 and persisted daily for one week. Pregnancy (5 weeks) was confirmed on 10/11/2021. Miscarriage of pregnancy occurred on 10/14/2021, 2 days after 2nd dose of Moderna Covid Vaccine.


VAERS ID: 1860490 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: Guam  
Vaccinated:2021-06-05
Onset:2021-10-13
   Days after vaccination:130
Submitted: 0000-00-00
Entered: 2021-11-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0168 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0168 / 2 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Maternal 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? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: eczema
Allergies: advil shellfish
Diagnostic Lab Data: FIRST TRIMESTER MISCARRIAGE CONFIRMED POST VACCINE BY ULTRASOUND AND BETA HCG Patient is recovering from physical and emotional trauma. Will continue to follow
CDC Split Type:

Write-up: positive UPT on 9/20/21 LMP July 2021 patient experienced vaginal bleeding consistent with miscarriage on 10/13/21-10/18/21


VAERS ID: 1794175 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Female  
Location: Nebraska  
Vaccinated:2021-10-12
Onset:2021-10-14
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-10-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 053E21A / 2 LA / SYR

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zyrtec, Montelukast, prenatal vitamin
Current Illness:
Preexisting Conditions: Became pregnant after 1st dose of Moderna Covid-19 vaccination. Due date approximately June 15, 2022. Miscarried pregnancy 2 days after second dose of Moderna Covid-19 vaccine. Gained Dr approval for both doses with knowledge of pregnancy or efforts to become pregnant.
Allergies: Idiopathic angioedema, triggers are unknown
Diagnostic Lab Data: Blood test on 10/16/21 confirmed miscarriage in progress. HCG ~ 25, Progesterone 0.9.
CDC Split Type:

Write-up: Moderna 1st dose received 9/14/21. Moderna Second dose received 10/12/21. I conceived on or around 9/26/21 and had a positive pregnancy test one day before 2nd dose. I miscarried the pregnancy on 10/14/21, two days after 2nd dose.


VAERS ID: 1840910 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-10-01
Onset:2021-10-14
   Days after vaccination:13
Submitted: 0000-00-00
Entered: 2021-11-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Chills, Dizziness, Fatigue, Foetal death, Nausea, Pyrexia, Stillbirth
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Termination of pregnancy and risk of abortion (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Crohn''s disease
Allergies:
Diagnostic Lab Data:
CDC Split Type: CHPFIZER INC202101415350

Write-up: still birth; Detection death fetus; Dizziness; Nausea; Fever attacks; Shivering; Tiredness/Exhaustion; This is a spontaneous report from a contactable consumer (patient). A pregnant female patient of an unspecified age received bnt162b2 (COMIRNATY), dose 2 via an unspecified route of administration on 01Oct2021 (Batch/Lot number was not reported) as dose 2, single for COVID-19 immunization. The patient previously received the first dose of bnt162b2 (COMIRNATY) on 03Sep2021 as single dose for COVID-19 immunization and experienced maternal exposure during pregnancy, second trimester. Medical history included Crohn''s disease. The patient''s concomitant medications were not reported. After the 2nd vaccination on an unspecified date in 2021, the patient experienced dizziness, nausea, fever attacks, shivering and tiredness/exhaustion. Determination of fetal death on 14Oct2021 and stillbirth on 16Oct2021. She was 22 Weeks pregnant at the onset of the event. The pregnancy resulted in still birth. The fetal outcome is intrauterine death. The outcome of the events was unknown. The lot number for BNT162b2 was not provided and will be requested during follow up.


VAERS ID: 1841872 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-09-30
Onset:2021-10-14
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-11-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2834 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Leiomyoma, Myalgia, Pregnancy test, Vaccination site swelling
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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: pregnancy test; Test Result: Positive ; Comments: She had a positive pregnancy test.
CDC Split Type: NLPFIZER INC202101437875

Write-up: Miscarriage; I estimate I was 2 weeks late. it looked like a tidal wave was coming out and I started to leak heavily. According to the doctor I found a fibroid in my underpants.; Reaction at or around the injection site: swelling, occurring within a week of vaccination; Myalgia; This is a spontaneous report from a contactable consumer (patient) downloaded from the Regulatory Agency (RA)-WEB and received via Regulatory Authority NL-LRB-00700609. This is first of two reports regarding 2nd dose of Comirnaty lot# FF2834. A 41-years-old pregnant female patient received second dose of bnt162b2 (COMIRNATY, solution for injection, Batch/Lot number: FF2834) via an unspecified route of administration on 31Sep2021 as DOSE 2, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient received first dose of bnt162b2 (COMIRNATY, solution for injection, Batch/Lot number: not reported) via an unspecified route of administration on 26Aug2021 as DOSE 1, SINGLE for covid-19 immunisation and had vaccine exposure during pregnancy week: 2. It was reported that the patient''s period was two weeks over time when she had a large bleeding with myoma, which was confirmed by her GP. The patient also reported a miscarriage at this time 14 days after the vaccine, which occurred at an estimated pregnancy duration of about 6 weeks. It was reported it took a while before patient period was due. It was estimated as 2 weeks late. When picking up her youngest at the facility, it looked like a tidal wave was coming out and patient started to leak heavily. According to the doctor, found a fibroid in patient underpants. A positive pregnancy test confirmed this. It was reported that this was the second Covid vaccination, which took place at a pregnancy duration of about 4 weeks and also had myalgia 1 hours after vaccine, injection site swelling 1 day after vaccine and myoma 14 days after the vaccine following administration. It was also reported that it was unclear whether the patient had a myoma as well as a miscarriage. The patient did not have Previous COVID-19 infection. The outcome of the events injection site swelling, and myalgia were recovered, myoma was recovering and other was unknown. Health Authority comments: BioNTech/Pfizer vaccine (Comirnaty): Past drug therapy BioNTech/Pfizer vaccine (Comirnaty): yes ADRs: no Date: 26Aug2021. Redness or Swelling: Extensive swelling of vaccinated limb: no; Sender''s Comments: Linked Report(s) : NL-PFIZER INC-202101447553 same patient , drug different dose


VAERS ID: 1814238 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-04-01
Onset:2021-10-15
   Days after vaccination:197
Submitted: 0000-00-00
Entered: 2021-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 AR / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 AR / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Caesarean section, Exposure during pregnancy, Foetal heart rate abnormal, Stillbirth
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: Prenatal
Current Illness: Nne
Preexisting Conditions: None
Allergies: N/A
Diagnostic Lab Data: Parents chose not to have an autopsy of their baby girl.
CDC Split Type:

Write-up: Baby born stillborn to vaccinated mother. Was pregnant at start of 2nd trimester when vaccine was received. Pregnancy seemed to progress uncomplicated. Due date was 10/8/21. Baby was moving around a s had a heartbeat on 10/8/21. A scheduled C-section was set for 10/15/21. Upon arrival to hospital for scheduled C-section baby was found to have no heartbeat and was born stillborn. Nothing visibly wrong with baby girl (e.g. no cord wrapped around neck, no obvious trauma or deformities not viable to life, etc.).


VAERS ID: 1819682 (history)  
Form: Version 2.0  
Age: 20.0  
Sex: Female  
Location: Hawaii  
Vaccinated:2021-09-23
Onset:2021-10-15
   Days after vaccination:22
Submitted: 0000-00-00
Entered: 2021-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30135BA / 1 LA / IM

Administered by: Military       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Exposure during pregnancy, Foetal heart rate abnormal, Foetal hypokinesia, Injection site pain, Pain in extremity, Ultrasound abdomen abnormal, Ultrasound scan vagina abnormal
SMQs:, Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Malignancy related therapeutic and diagnostic procedures (narrow), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), 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:
Other Medications: acetaminophen as needed
Current Illness: none
Preexisting Conditions: chronic hip pain; dyspareunia
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt is a female who was pregnant, estimated 7+ weeks gestation (LMP: 8/3/21, EDD: 5/10/22) when she received her COVID vaccine #1 on 23 SEP 21 following an appt with her PCM. She reported no significant events immediately following the vaccination. She reports soreness at the site of injection/left arm for one week. She reports having occasional mild abdominal cramping in the mornings, but did not think they were out of the ordinary. She otherwise felt well. On 15 OCT 21, she went to her scheduled initial OB appt. Both abdominal and vaginal ultrasounds were performed; no fetal movement or heartbeat was documented. The OB providers notified the pt of her miscarriage. Pt continues to follow up with OB for management.


VAERS ID: 1814737 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: New York  
Vaccinated:2021-10-15
Onset:2021-10-16
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-10-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 012F21A / 1 LA / IM

Administered by: Private       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? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamins
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: sonogram to confirm fetal demise scheduled for D&E in hospital
CDC Split Type:

Write-up: EDC 2/13/22 no fetal movements perceived beginning the day after receiving vaccine patient was 22w5d on day of vaccine no FHR was detected on 10/22/2021


VAERS ID: 1839622 (history)  
Form: Version 2.0  
Age: 25.0  
Sex: Female  
Location: Mississippi  
Vaccinated:2021-10-12
Onset:2021-10-16
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-11-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH 30145BA / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abortion spontaneous, Arthralgia, Asthenia, Chills, Diarrhoea, Dizziness, Exposure during pregnancy, Fatigue, Headache, Injection site pain, Injection site pruritus, Lethargy, Nausea, Pain, Pyrexia, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Arthritis (broad), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

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

Write-up: Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Diarrhea-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium, Systemic: Headache-Medium, Systemic: Joint Pain-Medium, Systemic: Nausea-Medium, Systemic: Vomiting-Medium, Systemic: Weakness-Medium, Additional Details: miscarriage


VAERS ID: 1859661 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-08-03
Onset:2021-10-18
   Days after vaccination:76
Submitted: 0000-00-00
Entered: 2021-11-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

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

Life Threatening? No
Birth Defect? Yes
Died? Yes
   Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Pregnancy (Patient no longer pregnant at the time of reporting.)
Allergies:
Diagnostic Lab Data: Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC202101507336

Write-up: cardiac abnormalities which unexpectedly worsened throughout pregnancy; Stillbirth; 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-202111022057260910-GZVE5, Safety Report Unique Identifier GB-MHRA-ADR 26152647. This is a spontaneous report from a contactable consumer received from the Regulatory Agency. The regulatory authority report number is GB-MHRA-WEBCOVID-202111022057260910-GZVE5. This consumer reported information for both mother and fetus/baby. This is a maternal report. A 31-year-old female patient received bnt162b2 (COMIRNATY, formulation: Solution for injection, Batch/Lot Number: not reported) via an unspecified route of administration on 03Aug2021 as dose 1, single for covid-19 immunisation. Medical history included pregnancy (not ongoing). Patient was no longer pregnant at the time of reporting. Concomitant medication included folic acid taken for vitamin supplementation. due date was 06Jan2022(28 weeks). On 18Oct2021, patient experienced stillbirth, on an unspecified date, cardiac abnormalities which unexpectedly worsened throughout pregnancy. Patient was exposed to the medicine Second-trimester (13-28 weeks). Stillbirth following cardiac abnormalities which unexpectedly worsened throughout pregnancy. The patient died on an unspecified date. An autopsy was not performed. Patient has not had symptoms associated with COVID-19. Patient was not currently breastfeeding. Report did not relate to possible inflammation of the heart (myocarditis or pericarditis). Lab test included sars-cov-2 test: no - negative covid-19 test. Fetal outcome was Intrauterine Death. The outcome of events was fatal. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Reported Cause(s) of Death: Stillbirth; cardiac abnormalities


VAERS ID: 1801018 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Arizona  
Vaccinated:2021-10-15
Onset:2021-10-19
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-10-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / IM

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

Life Threatening? No
Birth Defect? 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: levothyroxine, prenatal vitamins, folic acid, B6
Current Illness:
Preexisting Conditions: hypothyroid
Allergies: n/a
Diagnostic Lab Data: Confirmed on ultrasound 10/19/21
CDC Split Type:

Write-up: Spontaneous abortion


VAERS ID: 1801796 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-10-01
Onset:2021-10-19
   Days after vaccination:18
Submitted: 0000-00-00
Entered: 2021-10-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / IM

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Foetal death, Foetal vascular malperfusion, Induced labour, Premature delivery, Premature separation of placenta
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), 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? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: prenatal vitamins
Current Illness: gestational diabetes
Preexisting Conditions: obesity, asthma, hx of gastric bypass surgery (RNY)
Allergies: Cucumber, fish, lobster, watermelon NKDA
Diagnostic Lab Data:
CDC Split Type:

Write-up: Intrauterine fetal demise diagnosed on 10/19/21 when patient was 25 weeks and 5 day by an estimated delivery date of 1/27/22. She measured out to be 22 weeks 4 days by ultrasound. She was induced and delivered 10/20/21, with blood clot at placenta suggestive of placental abruption.


VAERS ID: 1818160 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Nebraska  
Vaccinated:2021-09-15
Onset:2021-10-20
   Days after vaccination:35
Submitted: 0000-00-00
Entered: 2021-10-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / SYR

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

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

Write-up: I had a miscarriage at 6 week. I went to my clinic where my doctor is. They did confirm that I had a miscarriage. The the lab work.


VAERS ID: 1822412 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: California  
Vaccinated:2021-10-12
Onset:2021-10-20
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-10-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 048C21A / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Abortion spontaneous, Exposure during pregnancy, Fear, Haemorrhage, Human chorionic gonadotropin, Pain, Pregnancy test urine negative, Pyrexia, Sleep disorder, Therapeutic response unexpected
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), 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: Prenatal vitamins
Current Illness:
Preexisting Conditions:
Allergies: Dairy, latex
Diagnostic Lab Data: Took urine pregnancy test and tested blood hcg to confirm miscarriage.
CDC Split Type:

Write-up: Miscarriage after receiving 2nd dose of vaccine. Was 9.5 weeks pregnant - due date May 21, 2022. Night of vaccine had fever and body aches, at 2am awoke and felt that my breasts were less tender/was very scared of miscarrying. Began to bleed 8 days after receiving vaccine.


VAERS ID: 1858516 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Guam  
Vaccinated:2021-04-07
Onset:2021-10-22
   Days after vaccination:198
Submitted: 0000-00-00
Entered: 2021-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8729 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER9735 / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Heavy menstrual bleeding, Muscle spasms, Pregnancy, Pregnancy test positive, Thrombosis, Ultrasound foetal abnormal
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Dystonia (broad), Thrombophlebitis (broad), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Limeperide 4mg Atrovastatin 10mg Jaidiance 25mg Amlodipine 5mg Lisinopril 10mg Metformin 1000mg
Current Illness: Diabetes Type 2, Hypertension
Preexisting Conditions: Diabetes Type 2, Hypertension
Allergies: Shellfish
Diagnostic Lab Data: FIRST TRIMESTER MISCARRIAGE CONFIRMED POST VACCINE BY ULTRASOUND patient is recovering from physical and emotional trauma. will continue to follow.
CDC Split Type:

Write-up: LMP JULY 2021 POSITIVE PREGNANCY TEST patient states cramping, blood clots, and heavy bleeding in October 2021, consistent with miscarriage


VAERS ID: 1858799 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Guam  
Vaccinated:2021-07-17
Onset:2021-10-22
   Days after vaccination:97
Submitted: 0000-00-00
Entered: 2021-11-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0168 / 1 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0168 / 2 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Abortion spontaneous, Emotional distress, Exposure during pregnancy, Injury, Ultrasound scan vagina, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Accidents and injuries (narrow), Hostility/aggression (broad), 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)

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: N/A
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: FIRST TRIMESTER MISCARRIAGE CONFIRMED POST VACCINE BY ULTRASOUND patient is recovering from physical and emotional trauma. Will continue to follow.
CDC Split Type:

Write-up: LMP 8/5/2021 first trimester miscarriage patient states vaginal bleeding consistent with miscarriage


VAERS ID: 1841643 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-10-08
Onset:2021-10-22
   Days after vaccination:14
Submitted: 0000-00-00
Entered: 2021-11-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: ASPIRIN [ACETYLSALICYLIC ACID]; CENTRUM PREGNANCY CARE; ENOXAPARIN; FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Blood transfusion (MOH requiring 5 units); Caesarean section (2x previous); Early miscarriage (2 x previous); Evacuation of retained products of conception (20/40- missed miscarriage); Suspected COVID-19 (Unsure when symptoms stopped)
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC202101439320

Write-up: Death intrauterine; This is a spontaneous report from a contactable healthcare professional. This is a report received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202110241416417470-CGRTB, Safety Report Unique Identifier GB-MHRA-ADR 26115054. A 38-year-old pregnant female patient received the first dose of BNT162b2 (COMIRNATY; Lot Number: UNKNOWN) via an unspecified route of administration on 08Oct2021 (at the age of 38-years-old), as a single dose for COVID-19 immunisation. The patient last menstrual date on 03Jun2021. Medical history included suspected COVID-19 on 30Mar2020, unsure when symptoms stopped. The patient previously had caesarean section (CS) twice, previous early miscarriage twice, 20/40- missed miscarriage and underwent evacuation of retained products of conception (ERPC) on an unknown date in Jun2020, MOH (as reported) required 5 units of blood transfused, pregnancy. Estimated due date is 10Mar2022. The patient did not have a COVID-19 test. The patient was not breastfeeding at the time of this report. The patient was not enrolled in clinical trial. Concomitant medications included acetylsalicylic acid (ASPIRIN) for antiphospholipid antibodies from 01Jul2021 to 23Oct2021, ascorbic acid/pyridoxine hydrochloride/biotin/folic acid/thiamine/nicotinic acid/pantothenic acid/riboflavin/betacarotene/iron/magnesium/manganese/copper/zinc/calcium/iodine/selenium/vitamin d nos/vitamin b12 nos/vitamin e nos (CENTRUM PREGNANCY CARE) for unknown indication from unknown date and unknown if ongoing, enoxaparin (MANUFACTURER UNKNOWN) for antiphospholipid antibodies positive from 01Jul2021 to 23Oct2021 and folic acid (MANUFACTURER UNKNOWN) for folic acid supplementation from unknown date and unknown if ongoing. Patient recieved BNT16B2 vaccine at 18+5 and exposed to the medicine second-trimester (13-28 weeks). The patient had intrauterine foetal death diagnosed at 20+5 on 22 Oct2021, and admitted for ERPC on 25Oct2021. The event did not relate to possible inflammation of the heart (myocarditis or pericarditis) and not relate to possible blood clots or low platelet counts. The patient had not tested positive for COVID-19 since the vaccination. The clinical outcome of the events death intrauterine was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


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