National Vaccine
Information Center

Your Health. Your Family. Your Choice.

MedAlerts.org
Search Results

From the 1/7/2022 release of VAERS data:

Found 3,499 cases where Vaccine is COVID19 and Symptom is Aborted pregnancy or Abortion or Abortion spontaneous or Abortion spontaneous complete or Abortion spontaneous incomplete or Abortion threatened or Foetal-maternal haemorrhage or Foetal cardiac disorder or Foetal damage or Foetal death or Foetal disorder or Foetal distress syndrome or Foetal heart rate abnormal or Foetal heart rate deceleration or Foetal heart rate deceleration abnormality or Foetal heart rate decreased or Foetal heart rate disorder or Foetal heart rate increased or Foetal hypokinesia or Foetal malformation or Foetal malpresentation or Foetal monitoring abnormal or Foetal movement disorder or Foetal movements decreased or Foetal non-stress test abnormal or Placental disorder or Pregnancy induced hypertension or Premature baby or Premature baby death or Premature delivery or Premature labour or Premature rupture of membranes or Premature separation of placenta or Stillbirth or Ultrasound foetal abnormal

Government Disclaimer on use of this data



Case Details

This is page 16 out of 350

Result pages: prev   7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25   next


VAERS ID: 1065910 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2020-12-30
Onset:2020-12-30
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011J20A / 1 - / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]; BONJESTA
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Miscarriage (18 May 2021); Pregnancy (live birth on 21 Feb 2016); Pregnancy (live birth on 08 Mar 2018)
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20210

Write-up: Miscarriage; Received vaccine when pregnant; A spontaneous report was received from a 34-year old female patient who received Moderna''s COVID-19 Vaccine (mRNA-1273) when pregnant and experienced a miscarriage. The patient''s medical history included three prior pregnancies, with two live births and one miscarriage. Products known to have been used by the patient, within two weeks prior to the event, included prenatal vitamins and doxylamine succinate/pyridoxine hydrochloride. The patient received their first of two planned doses of mRNA-1273 (Batch number: 011J20A) on 30 Dec 2020. On 27 Jan 2021, the patient received their second of two planned doses of mRNA-1273 (Batch number: 028L20A) intramuscularly for prophylaxis of COVID-19 infection. At 7 weeks gestation, the fetus had a normal heart beat. She reported that she had no complications with the pregnancy. On 08 Feb 2021, the patient had a miscarriage. Treatment information was not provided. The patient received both scheduled doses of mRNA-1273; therefore, action taken with the drug in response to the event is not applicable. The events received vaccine when pregnant and miscarriage were considered recovered.; Reporter''s Comments: This report concerns a 34-year-old, P2G4 who experienced miscarriage 1 month 9 days post administration of first dose and 12 days after the last dose of mRNA-1273 vaccine. There is not enough information such as the last menstrual period, estimated date of conception and delivery and gestational age at the time of miscarriage. In addition, the patient''s detailed medical history including any trauma and reason for previous miscarriage is lacking. Vaccine exposure during pregnancy is assessed as not applicable.


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

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021143584

Write-up: miscarried; patient was pregnant at the time of the vaccine; patient was pregnant at the time of the vaccine; This is a spontaneous report from a contactable healthcare professional reporting for herself. A 29-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number and expiry date not reported) via an unspecified route of administration at right arm, at the age of 29-year-old, on 30Jan2021 02:00 AM, single dose for COVID-19 immunization. Relevant medical history and concomitant medications were reported as none. The patient had no known allergies. The patient did not receive any other vaccine in four weeks or any other medications in two weeks. The patient was pregnant at the time of the vaccine 30Jan2021 and miscarried on 01Feb2021. LMP was provided as 01Jan2021, gestation period was reported as 4 weeks and due date was provided as 08Oct2021. The patient did not have covid prior vaccination and was not tested for covid post vaccination. The patient did not receive any treatment in response to the event miscarried. Outcome of the event miscarried was not recovered. Information on the lot/batch number has been requested.; Sender''s Comments: Based on the compatible temporal association, a possible contributory role of suspect vaccine BNT162B2 in triggering the misarrange in this 29-year-old pregnant patient cannot be excluded. Additional information regarding relevant medical history, underlying conditions, concomitant medications and detailed clinical course around the event onset will aid in comprehensive assessment of the case. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics committees and Investigators, as appropriate.


VAERS ID: 1065982 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2021-01-29
Onset:2021-01-30
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN5318 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood test, Muscle spasms, Premature separation of placenta, Shortened cervix, Ultrasound antenatal screen, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Dystonia (broad), 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? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Low dose aspirin doxylamine pyridoxine sudamenafin levothyroxine pre natal Pepcid
Current Illness: Hashimoto Thyroiditis Obesity in pregnancy Uterine Fibroids
Preexisting Conditions: Hashimoto Thyroiditis Obesity in pregnancy Uterine Fibroids
Allergies: Sulfa Cats
Diagnostic Lab Data: Ultrasound Lab work Blood test
CDC Split Type: vsafe

Write-up: **22 Weeks pregnant. Due date 7/1/21. 1st pregnancy** The day after the vaccine around 3pm I had cramps and light spotting. The nurse on call advised me to go to the ER. I went to ER, they ran an ultra sound and all kinds of test, they said everything looked good they thought it was a Fibroid. They discharged me, and that night at 11:30pm I had a very big and fast bleed around a cup of blood and went back to the ER. That time I went to hospital because it was closer. Again they did an ultrasound and thought it was a Fibroid. I ended up seeing my OB GYN 2/8/21, she said she didn''t think it was a Fibroid and sent me to get an ultrasound on 2/12/21. At that point after the bleed I had 4 days of spotting. When I went to the ultrasound they said I had a partial placenta abruption and my cervex has shortened. Since then everything has been fine.


VAERS ID: 1066027 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Minnesota  
Vaccinated:2021-02-17
Onset:2021-02-18
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 010M20A / 1 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Blood test, Exposure during pregnancy, Laboratory test, Premature delivery, Premature labour, Urine analysis
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? No
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Prenatal vitamin, iron supplement
Current Illness: None
Preexisting Conditions: None
Allergies: Sensitivity to penicillin
Diagnostic Lab Data: Admitted to Hospital late on 2/18/2021, was discharged on 2/21/2021. There were lots of tests and labs done due to the labor (e.g. urine analysis, bloodwork).
CDC Split Type:

Write-up: I was 34 weeks, 5 days pregnant at the time of vaccination (due date 3/26/2021). The next day at 10pm my water broke and I went into early labor. I had my baby on Friday in the early morning. Prior to this, I had no risks or warning signs of early labor (e.g. preeclampsia, gestational diabetes, etc) and was generally following a routine pregnancy path.


VAERS ID: 1066049 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: North Dakota  
Vaccinated:2021-01-06
Onset:2021-02-21
   Days after vaccination:46
Submitted: 0000-00-00
Entered: 2021-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 027L20A / 1 LA / IM

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: prenatal vitamins
Current Illness: none
Preexisting Conditions: none
Allergies: NKA
Diagnostic Lab Data: Ultra sound confirmed but dates not reported. No medical intervention reportedly needed to complete miscarriage.
CDC Split Type:

Write-up: Reported by patient to have been 9.5weeks pregnant when miscarriage happened.


VAERS ID: 1068246 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Georgia  
Vaccinated:2021-02-02
Onset:2021-02-01
Submitted: 0000-00-00
Entered: 2021-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / OT

Administered by: Private       Purchased by: ?
Symptoms: Exposure during pregnancy, Premature baby, Tachycardia foetal
SMQs:, Congenital and neonatal arrhythmias (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Foetal disorders (narrow), Neonatal disorders (narrow)

Life Threatening? No
Birth Defect? Yes
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 5 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021166927

Write-up: The baby had to be delivered at 35 3/7 weeks; Exposure during pregnancy; Fetal tachycardia noted 1 week after the 2nd dose of the vaccine. The infant had to be delivered at 35 3/7 weeks due to non-reassuring status during monitoring; This is a Spontaneous report from a contactable physician. This physician reported information for a mother and baby. This is baby report. A neonate''s mother (mother was reported as 35-year-old) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: UNKNOWN ), intramuscular on 02Feb2021 as a single dose for COVID-19 immunization. The patients mothers medical history and concomitant medications were not reported. The baby experienced fetal tachycardia noted 1 week after the 2nd dose of the vaccine in Feb2021 (also reported as 02Feb2021). The baby had to be delivered at 35 3/7 weeks due to non-reassuring status during monitoring on. The patient was hospitalized for 5 days. The clinical outcome of Fetal tachycardia noted 1 week after the 2nd dose of the vaccine. The baby had to be delivered at 35 3/7 weeks due to non-reassuring status during monitoring was unknown. Information on lot number was requested.; Sender''s Comments: Based on the available information a causal relationship between events "fetal tachycardia noted 1 week after the 2nd dose of the vaccine" and "the baby had to be delivered at 35 3/7 weeks" and BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) cannot be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.,Linked Report(s) : US-PFIZER INC-2021166872 mother/fetus


VAERS ID: 1069747 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-01-06
Onset:2021-02-18
   Days after vaccination:43
Submitted: 0000-00-00
Entered: 2021-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL9261 / 2 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Abdominal pain, Abortion spontaneous, Foetal heart rate abnormal, Laboratory test, Muscle spasms, Ultrasound scan
SMQs:, Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Dystonia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Foetal disorders (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Prenatal
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Ultrasound 2/26 Blood work and ultrasound 2/27 Ultrasound 2/21
CDC Split Type:

Write-up: Became pregnant end of December. Received first dose January 6 and second dose January 27. Had very bad side effects. Felt pregnancy symptoms up until February 10th. Symptoms started to linger off. Had ultrasound that showed fetus February 10. Cramping started feeling days later. Had ultrasound again February 18 showed fetus had grown. Had another ultrasound February 21 after going to ED for bad cramping and pain. fetus had no heart beat. Miscarried February 26. Contents did not pass completely, had D&C February 27.


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

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

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

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


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

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

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

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


VAERS ID: 1070733 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-01-08
Onset:2021-01-11
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / OT

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

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021182471

Write-up: miscarriage; This is a spontaneous report from a contactable nurse (patient). A 30-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), 2nd dose on 08Jan2021 in right arm and 1st dose on 15Dec2020 in left arm, both via intramuscular at single dose for COVID-19 immunisation. The patient medical history was not reported. The patient previously took amoxicillin and experienced allergy. Concomitant medication included prenatal vitamins. The patient experienced miscarriage on 11Jan2021 with outcome of recovered. The event resulted in doctor or other healthcare professional office/clinic visit. The mother reported she became pregnant while taking bnt162b2. The mother was 11 weeks pregnant at the onset of the event. The mother was due to deliver on 07Aug2021. Date of LMP was 26Oct2020. Therapeutic measures were taken as a result of miscarriage included misoprostol (CYTOTEC). Information of lot/batch number has been requested.; Sender''s Comments: The limited information provided precludes a full clinical assessment of the case. Considering the product-event temporal relationship, a causal association between the reported ''miscarriage'' and the administration of bnt162b2 cannot be completely excluded. Case will be reassessed once with additional information. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate.


Result pages: prev   7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25   next

New Search

Link To This Search Result:

https://www.medalerts.org/vaersdb/findfield.php?EVENTS=ON&PAGENO=16&SYMPTOMS[]=Aborted_pregnancy_%2810000209%29&SYMPTOMS[]=Abortion_%2810000210%29&SYMPTOMS[]=Abortion_spontaneous_%2810000234%29&SYMPTOMS[]=Abortion_spontaneous_complete_%2810061616%29&SYMPTOMS[]=Abortion_spontaneous_incomplete_%2810061617%29&SYMPTOMS[]=Abortion_threatened_%2810000242%29&SYMPTOMS[]=Foetal-maternal_haemorrhage_%2810016871%29&SYMPTOMS[]=Foetal_cardiac_disorder_%2810052088%29&SYMPTOMS[]=Foetal_damage_%2810016852%29&SYMPTOMS[]=Foetal_death_%2810055690%29&SYMPTOMS[]=Foetal_disorder_%2810061157%29&SYMPTOMS[]=Foetal_distress_syndrome_%2810016855%29&SYMPTOMS[]=Foetal_heart_rate_abnormal_%2810051139%29&SYMPTOMS[]=Foetal_heart_rate_deceleration_%2810058322%29&SYMPTOMS[]=Foetal_heart_rate_deceleration_abnormality_%2810074636%29&SYMPTOMS[]=Foetal_heart_rate_decreased_%2810051136%29&SYMPTOMS[]=Foetal_heart_rate_disorder_%2810061158%29&SYMPTOMS[]=Foetal_heart_rate_increased_%2810051138%29&SYMPTOMS[]=Foetal_hypokinesia_%2810068461%29&SYMPTOMS[]=Foetal_malformation_%2810060919%29&SYMPTOMS[]=Foetal_malpresentation_%2810058013%29&SYMPTOMS[]=Foetal_monitoring_abnormal_%2810071507%29&SYMPTOMS[]=Foetal_movement_disorder_%2810077576%29&SYMPTOMS[]=Foetal_movements_decreased_%2810016866%29&SYMPTOMS[]=Foetal_non-stress_test_abnormal_%2810071516%29&SYMPTOMS[]=Placental_disorder_%2810035132%29&SYMPTOMS[]=Pregnancy_induced_hypertension_%2810036563%29&SYMPTOMS[]=Premature_baby_%2810036590%29&SYMPTOMS[]=Premature_baby_death_%2810076700%29&SYMPTOMS[]=Premature_delivery_%2810036595%29&SYMPTOMS[]=Premature_labour_%2810036600%29&SYMPTOMS[]=Premature_rupture_of_membranes_%2810036603%29&SYMPTOMS[]=Premature_separation_of_placenta_%2810036608%29&SYMPTOMS[]=Stillbirth_%2810042062%29&SYMPTOMS[]=Ultrasound_foetal_abnormal_%2810077578%29&VAX=COVID19


Copyright © 2022 National Vaccine Information Center. All rights reserved.
21525 Ridgetop Circle, Suite 100, Sterling, VA 20166