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This is VAERS ID 278375

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History of Changes from the VAERS Wayback Machine

First Appeared on 12/31/2007

VAERS ID: 278375
VAERS Form:
Age:35.0
Sex:Female
Location:Unknown
Vaccinated:2007-02-28
Onset:2007-02-28
Submitted:2007-05-10
Entered:2007-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / - UN / UN

Administered by: Other      Purchased by: Unknown
Symptoms: Abortion induced, Ectopic pregnancy, Drug exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type':

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vac"cinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termina


Changed on 12/8/2009

VAERS ID: 278375 Before After
VAERS Form:
Age:35.0
Sex:Female
Location:Unknown
Vaccinated:2007-02-28
Onset:2007-02-28
Submitted:2007-05-10
Entered:2007-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / - UN / UN

Administered by: Other      Purchased by: Unknown Other
Symptoms: Abortion induced, Ectopic pregnancy, Drug exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': (blank) WAES0704USA03486

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vac"cinated vaccinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termina termination of the initial pregnancy had "failed", or whether this is a second pregnancy. Unspecified medical attention was sought. There was no product quality complaint. Follow up information has been received through the manufacturer Pregnancy Registry from a healthcare worker who reported that the patient, who had no previous pertinent medical history, developed an ectopic pregnancy, and was given methotrexate to induce an abortion. The patient was not recovered at the time of reporting. There was no product quality complaint. Additional information has been requested.


Changed on 9/14/2017

VAERS ID: 278375 Before After
VAERS Form:(blank) 1
Age:35.0
Sex:Female
Location:Unknown
Vaccinated:2007-02-28
Onset:2007-02-28
Submitted:2007-05-10
Entered:2007-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / - UNK UN / UN

Administered by: Other      Purchased by: Other
Symptoms: Abortion induced, Ectopic pregnancy, Drug exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0704USA03486

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vaccinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termination of the initial pregnancy had "failed", or whether this is a second pregnancy. Unspecified medical attention was sought. There was no product quality complaint. Follow up information has been received through the manufacturer Pregnancy Registry from a healthcare worker who reported that the patient, who had no previous pertinent medical history, developed an ectopic pregnancy, and was given methotrexate to induce an abortion. The patient was not recovered at the time of reporting. There was no product quality complaint. Additional information has been requested.


Changed on 2/14/2018

VAERS ID: 278375 Before After
VAERS Form:1
Age:35.0
Sex:Female
Location:Unknown
Vaccinated:2007-02-28
Onset:2007-02-28
Submitted:2007-05-10
Entered:2007-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other      Purchased by: Other
Symptoms: Abortion induced, Ectopic pregnancy, Drug exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0704USA03486

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vaccinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termination of the initial pregnancy had "failed", or whether this is a second pregnancy. Unspecified medical attention was sought. There was no product quality complaint. Follow up information has been received through the manufacturer Pregnancy Registry from a healthcare worker who reported that the patient, who had no previous pertinent medical history, developed an ectopic pregnancy, and was given methotrexate to induce an abortion. The patient was not recovered at the time of reporting. There was no product quality complaint. Additional information has been requested.


Changed on 6/14/2018

VAERS ID: 278375 Before After
VAERS Form:1
Age:35.0
Sex:Female
Location:Unknown
Vaccinated:2007-02-28
Onset:2007-02-28
Submitted:2007-05-10
Entered:2007-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other      Purchased by: Other
Symptoms: Abortion induced, Ectopic pregnancy, Drug exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0704USA03486

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vaccinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termination of the initial pregnancy had "failed", or whether this is a second pregnancy. Unspecified medical attention was sought. There was no product quality complaint. Follow up information has been received through the manufacturer Pregnancy Registry from a healthcare worker who reported that the patient, who had no previous pertinent medical history, developed an ectopic pregnancy, and was given methotrexate to induce an abortion. The patient was not recovered at the time of reporting. There was no product quality complaint. Additional information has been requested.


Changed on 8/14/2018

VAERS ID: 278375 Before After
VAERS Form:1
Age:35.0
Sex:Female
Location:Unknown
Vaccinated:2007-02-28
Onset:2007-02-28
Submitted:2007-05-10
Entered:2007-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other      Purchased by: Other
Symptoms: Abortion induced, Ectopic pregnancy, Drug exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0704USA03486

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vaccinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termination of the initial pregnancy had "failed", or whether this is a second pregnancy. Unspecified medical attention was sought. There was no product quality complaint. Follow up information has been received through the manufacturer Pregnancy Registry from a healthcare worker who reported that the patient, who had no previous pertinent medical history, developed an ectopic pregnancy, and was given methotrexate to induce an abortion. The patient was not recovered at the time of reporting. There was no product quality complaint. Additional information has been requested.


Changed on 9/14/2018

VAERS ID: 278375 Before After
VAERS Form:1
Age:35.0
Sex:Female
Location:Unknown
Vaccinated:2007-02-28
Onset:2007-02-28
Submitted:2007-05-10
Entered:2007-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other      Purchased by: Other
Symptoms: Abortion induced, Ectopic pregnancy, Drug exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0704USA03486

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vaccinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termination of the initial pregnancy had "failed", or whether this is a second pregnancy. Unspecified medical attention was sought. There was no product quality complaint. Follow up information has been received through the manufacturer Pregnancy Registry from a healthcare worker who reported that the patient, who had no previous pertinent medical history, developed an ectopic pregnancy, and was given methotrexate to induce an abortion. The patient was not recovered at the time of reporting. There was no product quality complaint. Additional information has been requested.


Changed on 10/14/2018

VAERS ID: 278375 Before After
VAERS Form:1
Age:35.0
Sex:Female
Location:Unknown
Vaccinated:2007-02-28
Onset:2007-02-28
Submitted:2007-05-10
Entered:2007-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other      Purchased by: Other
Symptoms: Abortion induced, Ectopic pregnancy, Drug exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0704USA03486

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vaccinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termination of the initial pregnancy had "failed", or whether this is a second pregnancy. Unspecified medical attention was sought. There was no product quality complaint. Follow up information has been received through the manufacturer Pregnancy Registry from a healthcare worker who reported that the patient, who had no previous pertinent medical history, developed an ectopic pregnancy, and was given methotrexate to induce an abortion. The patient was not recovered at the time of reporting. There was no product quality complaint. Additional information has been requested.


Changed on 12/24/2020

VAERS ID: 278375 Before After
VAERS Form:1
Age:35.0
Sex:Female
Location:Unknown
Vaccinated:2007-02-28
Onset:2007-02-28
Submitted:2007-05-10
Entered:2007-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other      Purchased by: Other
Symptoms: Abortion induced, Ectopic pregnancy, Drug exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0704USA03486

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vaccinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termination of the initial pregnancy had "failed", or whether this is a second pregnancy. Unspecified medical attention was sought. There was no product quality complaint. Follow up information has been received through the manufacturer Pregnancy Registry from a healthcare worker who reported that the patient, who had no previous pertinent medical history, developed an ectopic pregnancy, and was given methotrexate to induce an abortion. The patient was not recovered at the time of reporting. There was no product quality complaint. Additional information has been requested.


Changed on 12/30/2020

VAERS ID: 278375 Before After
VAERS Form:1
Age:35.0
Sex:Female
Location:Unknown
Vaccinated:2007-02-28
Onset:2007-02-28
Submitted:2007-05-10
Entered:2007-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other      Purchased by: Other
Symptoms: Abortion induced, Ectopic pregnancy, Drug exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0704USA03486

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vaccinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termination of the initial pregnancy had "failed", or whether this is a second pregnancy. Unspecified medical attention was sought. There was no product quality complaint. Follow up information has been received through the manufacturer Pregnancy Registry from a healthcare worker who reported that the patient, who had no previous pertinent medical history, developed an ectopic pregnancy, and was given methotrexate to induce an abortion. The patient was not recovered at the time of reporting. There was no product quality complaint. Additional information has been requested.


Changed on 5/7/2021

VAERS ID: 278375 Before After
VAERS Form:1
Age:35.0
Sex:Female
Location:Unknown
Vaccinated:2007-02-28
Onset:2007-02-28
Submitted:2007-05-10
Entered:2007-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other      Purchased by: Other
Symptoms: Abortion induced, Ectopic pregnancy, Drug exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0704USA03486

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vaccinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termination of the initial pregnancy had "failed", or whether this is a second pregnancy. Unspecified medical attention was sought. There was no product quality complaint. Follow up information has been received through the manufacturer Pregnancy Registry from a healthcare worker who reported that the patient, who had no previous pertinent medical history, developed an ectopic pregnancy, and was given methotrexate to induce an abortion. The patient was not recovered at the time of reporting. There was no product quality complaint. Additional information has been requested.


Changed on 5/21/2021

VAERS ID: 278375 Before After
VAERS Form:1
Age:35.0
Sex:Female
Location:Unknown
Vaccinated:2007-02-28
Onset:2007-02-28
Submitted:2007-05-10
Entered:2007-05-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other      Purchased by: Other
Symptoms: Abortion induced, Ectopic pregnancy, Drug exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0704USA03486

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vaccinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termination of the initial pregnancy had "failed", or whether this is a second pregnancy. Unspecified medical attention was sought. There was no product quality complaint. Follow up information has been received through the manufacturer Pregnancy Registry from a healthcare worker who reported that the patient, who had no previous pertinent medical history, developed an ectopic pregnancy, and was given methotrexate to induce an abortion. The patient was not recovered at the time of reporting. There was no product quality complaint. Additional information has been requested.

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