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This is VAERS ID 817276

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History of Changes from the VAERS Wayback Machine

First Appeared on 6/14/2019

VAERS ID: 817276
VAERS Form:2
Age:
Sex:Unknown
Location:Unknown
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted:0000-00-00
Entered:2019-06-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK UN / UN

Administered by: Unknown      Purchased by: ??
Symptoms: Death, Pneumonia, Respiratory failure

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died:0000-00-00
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: HIV infection
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': USGLAXOSMITHKLINEUS2019GS

Write-up: This case was reported in a literature article and described the occurrence of respiratory failure in a infant subject who received Rotavirus vaccine for prophylaxis. Concurrent medical conditions included HIV infection. On an unknown date, unknown after receiving Rotavirus vaccine, the subject developed respiratory failure. Serious criteria included death and GSK medically significant. Additional event(s) included pneumonia with serious criteria of GSK medically significant. The outcome of respiratory failure was fatal. The outcome(s) of the additional event(s) included pneumonia (unknown). The reported cause of death was respiratory failure. The investigator considered that there was a reasonable possibility that the respiratory failure and pneumonia may have been caused by Rotavirus vaccine. Additional information was provided. This case was reported in a literature article and described the occurrence of pneumonia and respiratory failure in an infant of unspecified age and gender who was vaccinated with unspecified rotavirus vaccine (manufacturer unknown) for prophylaxis. This case corresponds to table 1 reported in this literature article. The patient was part of the study that characterize adverse events (AE) after rotavirus (RV) in infants with immunocompromising conditions (IC) reported to the Vaccine Adverse Event Reporting System (VAERS) from February 2006 to December 2015. The patient had human immunodeficiency virus (HIV) infection. No information on patient''s medical or family history or concomitant medication were provided. On an unspecified date, the patient received unspecified rotavirus virus vaccine (administration route and site unspecified, dosage unknown; batch number not provided). The age of vaccination was not provided. On an unspecified date, an unknown period after vaccination, the patient developed pneumonia. On an unspecified date, the patient died. The cause of death was respiratory failure. It was unknown if an autopsy was performed. This case has been considered as serious due to death. The treatment was unknown. The author stated and concluded, "Adverse event (AE) after RV in immunocompromised infants are rarely reported to VAERS, but most are clinically serious events. Additional data would be helpful in assessing the safety of RV in non-SCID IC including in-utero exposure to monoclonal antibodies MAB". This is 1 of the 11 valid cases reported in this literature article. The article corresponding to this case is not available for submission due to copyright restriction. Reported Cause(s) of Death: Respiratory failure.


Changed on 12/10/2020

VAERS ID: 817276 Before After
VAERS Form:2
Age:
Sex:Unknown
Location:Unknown Georgia
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted:0000-00-00
Entered:2019-06-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK UN / UN

Administered by: Unknown      Purchased by: ??
Symptoms: Death, Pneumonia, Respiratory failure

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died:0000-00-00
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: HIV infection
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': USGLAXOSMITHKLINEUS2019GS

Write-up: This case was reported in a literature article and described the occurrence of respiratory failure in a infant subject who received Rotavirus vaccine for prophylaxis. Concurrent medical conditions included HIV infection. On an unknown date, unknown after receiving Rotavirus vaccine, the subject developed respiratory failure. Serious criteria included death and GSK medically significant. Additional event(s) included pneumonia with serious criteria of GSK medically significant. The outcome of respiratory failure was fatal. The outcome(s) of the additional event(s) included pneumonia (unknown). The reported cause of death was respiratory failure. The investigator considered that there was a reasonable possibility that the respiratory failure and pneumonia may have been caused by Rotavirus vaccine. Additional information was provided. This case was reported in a literature article and described the occurrence of pneumonia and respiratory failure in an infant of unspecified age and gender who was vaccinated with unspecified rotavirus vaccine (manufacturer unknown) for prophylaxis. This case corresponds to table 1 reported in this literature article. The patient was part of the study that characterize adverse events (AE) after rotavirus (RV) in infants with immunocompromising conditions (IC) reported to the Vaccine Adverse Event Reporting System (VAERS) from February 2006 to December 2015. The patient had human immunodeficiency virus (HIV) infection. No information on patient''s medical or family history or concomitant medication were provided. On an unspecified date, the patient received unspecified rotavirus virus vaccine (administration route and site unspecified, dosage unknown; batch number not provided). The age of vaccination was not provided. On an unspecified date, an unknown period after vaccination, the patient developed pneumonia. On an unspecified date, the patient died. The cause of death was respiratory failure. It was unknown if an autopsy was performed. This case has been considered as serious due to death. The treatment was unknown. The author stated and concluded, "Adverse event (AE) after RV in immunocompromised infants are rarely reported to VAERS, but most are clinically serious events. Additional data would be helpful in assessing the safety of RV in non-SCID IC including in-utero exposure to monoclonal antibodies MAB". This is 1 of the 11 valid cases reported in this literature article. The article corresponding to this case is not available for submission due to copyright restriction. Reported Cause(s) of Death: Respiratory failure.


Changed on 12/24/2020

VAERS ID: 817276 Before After
VAERS Form:2
Age:
Sex:Unknown
Location:Georgia
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted:0000-00-00
Entered:2019-06-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK UN / UN

Administered by: Unknown      Purchased by: ??
Symptoms: Death, Pneumonia, Respiratory failure

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died:0000-00-00
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: HIV infection
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': USGLAXOSMITHKLINEUS2019GS

Write-up: This case was reported in a literature article and described the occurrence of respiratory failure in a infant subject who received Rotavirus vaccine for prophylaxis. Concurrent medical conditions included HIV infection. On an unknown date, unknown after receiving Rotavirus vaccine, the subject developed respiratory failure. Serious criteria included death and GSK medically significant. Additional event(s) included pneumonia with serious criteria of GSK medically significant. The outcome of respiratory failure was fatal. The outcome(s) of the additional event(s) included pneumonia (unknown). The reported cause of death was respiratory failure. The investigator considered that there was a reasonable possibility that the respiratory failure and pneumonia may have been caused by Rotavirus vaccine. Additional information was provided. This case was reported in a literature article and described the occurrence of pneumonia and respiratory failure in an infant of unspecified age and gender who was vaccinated with unspecified rotavirus vaccine (manufacturer unknown) for prophylaxis. This case corresponds to table 1 reported in this literature article. The patient was part of the study that characterize adverse events (AE) after rotavirus (RV) in infants with immunocompromising conditions (IC) reported to the Vaccine Adverse Event Reporting System (VAERS) from February 2006 to December 2015. The patient had human immunodeficiency virus (HIV) infection. No information on patient''s medical or family history or concomitant medication were provided. On an unspecified date, the patient received unspecified rotavirus virus vaccine (administration route and site unspecified, dosage unknown; batch number not provided). The age of vaccination was not provided. On an unspecified date, an unknown period after vaccination, the patient developed pneumonia. On an unspecified date, the patient died. The cause of death was respiratory failure. It was unknown if an autopsy was performed. This case has been considered as serious due to death. The treatment was unknown. The author stated and concluded, "Adverse event (AE) after RV in immunocompromised infants are rarely reported to VAERS, but most are clinically serious events. Additional data would be helpful in assessing the safety of RV in non-SCID IC including in-utero exposure to monoclonal antibodies MAB". This is 1 of the 11 valid cases reported in this literature article. The article corresponding to this case is not available for submission due to copyright restriction. Reported Cause(s) of Death: Respiratory failure.


Changed on 12/30/2020

VAERS ID: 817276 Before After
VAERS Form:2
Age:
Sex:Unknown
Location:Georgia
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted:0000-00-00
Entered:2019-06-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK UN / UN

Administered by: Unknown      Purchased by: ??
Symptoms: Death, Pneumonia, Respiratory failure

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died:0000-00-00
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: HIV infection
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': USGLAXOSMITHKLINEUS2019GS

Write-up: This case was reported in a literature article and described the occurrence of respiratory failure in a infant subject who received Rotavirus vaccine for prophylaxis. Concurrent medical conditions included HIV infection. On an unknown date, unknown after receiving Rotavirus vaccine, the subject developed respiratory failure. Serious criteria included death and GSK medically significant. Additional event(s) included pneumonia with serious criteria of GSK medically significant. The outcome of respiratory failure was fatal. The outcome(s) of the additional event(s) included pneumonia (unknown). The reported cause of death was respiratory failure. The investigator considered that there was a reasonable possibility that the respiratory failure and pneumonia may have been caused by Rotavirus vaccine. Additional information was provided. This case was reported in a literature article and described the occurrence of pneumonia and respiratory failure in an infant of unspecified age and gender who was vaccinated with unspecified rotavirus vaccine (manufacturer unknown) for prophylaxis. This case corresponds to table 1 reported in this literature article. The patient was part of the study that characterize adverse events (AE) after rotavirus (RV) in infants with immunocompromising conditions (IC) reported to the Vaccine Adverse Event Reporting System (VAERS) from February 2006 to December 2015. The patient had human immunodeficiency virus (HIV) infection. No information on patient''s medical or family history or concomitant medication were provided. On an unspecified date, the patient received unspecified rotavirus virus vaccine (administration route and site unspecified, dosage unknown; batch number not provided). The age of vaccination was not provided. On an unspecified date, an unknown period after vaccination, the patient developed pneumonia. On an unspecified date, the patient died. The cause of death was respiratory failure. It was unknown if an autopsy was performed. This case has been considered as serious due to death. The treatment was unknown. The author stated and concluded, "Adverse event (AE) after RV in immunocompromised infants are rarely reported to VAERS, but most are clinically serious events. Additional data would be helpful in assessing the safety of RV in non-SCID IC including in-utero exposure to monoclonal antibodies MAB". This is 1 of the 11 valid cases reported in this literature article. The article corresponding to this case is not available for submission due to copyright restriction. Reported Cause(s) of Death: Respiratory failure.


Changed on 5/7/2021

VAERS ID: 817276 Before After
VAERS Form:2
Age:
Sex:Unknown
Location:Georgia
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted:0000-00-00
Entered:2019-06-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK UN / UN

Administered by: Unknown      Purchased by: ??
Symptoms: Death, Pneumonia, Respiratory failure

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died:0000-00-00
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: HIV infection
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': USGLAXOSMITHKLINEUS2019GS

Write-up: This case was reported in a literature article and described the occurrence of respiratory failure in a infant subject who received Rotavirus vaccine for prophylaxis. Concurrent medical conditions included HIV infection. On an unknown date, unknown after receiving Rotavirus vaccine, the subject developed respiratory failure. Serious criteria included death and GSK medically significant. Additional event(s) included pneumonia with serious criteria of GSK medically significant. The outcome of respiratory failure was fatal. The outcome(s) of the additional event(s) included pneumonia (unknown). The reported cause of death was respiratory failure. The investigator considered that there was a reasonable possibility that the respiratory failure and pneumonia may have been caused by Rotavirus vaccine. Additional information was provided. This case was reported in a literature article and described the occurrence of pneumonia and respiratory failure in an infant of unspecified age and gender who was vaccinated with unspecified rotavirus vaccine (manufacturer unknown) for prophylaxis. This case corresponds to table 1 reported in this literature article. The patient was part of the study that characterize adverse events (AE) after rotavirus (RV) in infants with immunocompromising conditions (IC) reported to the Vaccine Adverse Event Reporting System (VAERS) from February 2006 to December 2015. The patient had human immunodeficiency virus (HIV) infection. No information on patient''s medical or family history or concomitant medication were provided. On an unspecified date, the patient received unspecified rotavirus virus vaccine (administration route and site unspecified, dosage unknown; batch number not provided). The age of vaccination was not provided. On an unspecified date, an unknown period after vaccination, the patient developed pneumonia. On an unspecified date, the patient died. The cause of death was respiratory failure. It was unknown if an autopsy was performed. This case has been considered as serious due to death. The treatment was unknown. The author stated and concluded, "Adverse event (AE) after RV in immunocompromised infants are rarely reported to VAERS, but most are clinically serious events. Additional data would be helpful in assessing the safety of RV in non-SCID IC including in-utero exposure to monoclonal antibodies MAB". This is 1 of the 11 valid cases reported in this literature article. The article corresponding to this case is not available for submission due to copyright restriction. Reported Cause(s) of Death: Respiratory failure.


Changed on 5/21/2021

VAERS ID: 817276 Before After
VAERS Form:2
Age:
Sex:Unknown
Location:Georgia
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted:0000-00-00
Entered:2019-06-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK UN / UN

Administered by: Unknown      Purchased by: ??
Symptoms: Death, Pneumonia, Respiratory failure

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died:0000-00-00
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: HIV infection
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': USGLAXOSMITHKLINEUS2019GS

Write-up: This case was reported in a literature article and described the occurrence of respiratory failure in a infant subject who received Rotavirus vaccine for prophylaxis. Concurrent medical conditions included HIV infection. On an unknown date, unknown after receiving Rotavirus vaccine, the subject developed respiratory failure. Serious criteria included death and GSK medically significant. Additional event(s) included pneumonia with serious criteria of GSK medically significant. The outcome of respiratory failure was fatal. The outcome(s) of the additional event(s) included pneumonia (unknown). The reported cause of death was respiratory failure. The investigator considered that there was a reasonable possibility that the respiratory failure and pneumonia may have been caused by Rotavirus vaccine. Additional information was provided. This case was reported in a literature article and described the occurrence of pneumonia and respiratory failure in an infant of unspecified age and gender who was vaccinated with unspecified rotavirus vaccine (manufacturer unknown) for prophylaxis. This case corresponds to table 1 reported in this literature article. The patient was part of the study that characterize adverse events (AE) after rotavirus (RV) in infants with immunocompromising conditions (IC) reported to the Vaccine Adverse Event Reporting System (VAERS) from February 2006 to December 2015. The patient had human immunodeficiency virus (HIV) infection. No information on patient''s medical or family history or concomitant medication were provided. On an unspecified date, the patient received unspecified rotavirus virus vaccine (administration route and site unspecified, dosage unknown; batch number not provided). The age of vaccination was not provided. On an unspecified date, an unknown period after vaccination, the patient developed pneumonia. On an unspecified date, the patient died. The cause of death was respiratory failure. It was unknown if an autopsy was performed. This case has been considered as serious due to death. The treatment was unknown. The author stated and concluded, "Adverse event (AE) after RV in immunocompromised infants are rarely reported to VAERS, but most are clinically serious events. Additional data would be helpful in assessing the safety of RV in non-SCID IC including in-utero exposure to monoclonal antibodies MAB". This is 1 of the 11 valid cases reported in this literature article. The article corresponding to this case is not available for submission due to copyright restriction. Reported Cause(s) of Death: Respiratory failure.

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