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This is VAERS ID 268712

History of Changes from the VAERS Wayback Machine

First Appeared on 12/30/2006

VAERS ID: 268712
VAERS Form:
Age:0.2
Gender:Male
Location:Washington
Vaccinated:2006-08-17
Onset:2006-09-28
Submitted:2006-12-08
Entered:2006-12-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (UNKNOWN MFR) / UNKNOWN MANUFACTURER - / - - / -
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. - / - - / -
HIBV: HIB (ACTHIB) / AVENTIS PASTEUR, INC. - / - - / -
ROTHB5: ROTAVIRUS VACCINE, LIVE, ORAL, PENTAVALENT (ROTATEQ) / MERCK & CO. INC. 0146F / 2 - / PO

Administered by: Other      Purchased by: Unknown
Symptoms: Intussusception, Irritability, Pyrexia, Viral infection, Vomiting

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 1     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: 8/2/06 X Ray normal, diagnostic lab normal, body temp fever.
CDC 'Split Type':

Write-up: Information has been received from a physician concerning a 23 week old male, with no significant medical history, who, on 16-Jun-2006 was vaccinated with an oral, 2.0 ml, first dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine) (Lot"#653661/0146F). Concomitant vaccination administered on 16-Jun-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), and a dose if hepatitis B vir


Changed on 12/8/2009

VAERS ID: 268712 Before After
VAERS Form:
Age:0.2
Gender:Male
Location:Washington
Vaccinated:2006-08-17
Onset:2006-09-28
Submitted:2006-12-08
Entered:2006-12-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (UNKNOWN MFR) DTAP (NO BRAND NAME) / UNKNOWN MANUFACTURER - / - - / -
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. - / - - / -
HIBV: HIB (ACTHIB) / AVENTIS PASTEUR, INC. AVENTIS PASTEUR - / - - / -
ROTHB5: ROTAVIRUS VACCINE, LIVE, ORAL, PENTAVALENT (ROTATEQ) ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0146F / 2 - / PO

Administered by: Other      Purchased by: Unknown Other
Symptoms: Intussusception, Irritability, Pyrexia, Viral infection, Vomiting

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 1     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: 8/2/06 X Ray normal, diagnostic lab normal, body temp fever.
CDC 'Split Type': (blank) WAES0612USA00126

Write-up: Information has been received from a physician concerning a 23 week old male, with no significant medical history, who, on 16-Jun-2006 was vaccinated with an oral, 2.0 ml, first dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine) (Lot"#653661/0146F). (Lot#653661/0146F). Concomitant vaccination administered on 16-Jun-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), and a dose if hepatitis B vir virus vaccine rHBsAg (yeast). On 14-Jul-2006 the patient was vaccinated with a second 2.0 ml oral dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine). There were no concomitant vaccinations given on 14-Jul-2006. In July 2006 the patient was noted to have fallen out of a shopping cart. On 02-Aug-2006 the patient developed a fever. The patient was taken to the emergency room where an x-ray and labs (not further specified) were normal. No formal diagnosis was made and the patient was simply thought to have a virus. On 17-Aug-2006 the patient was vaccinated with a third 2.0 ml oral dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine). Concomitant vaccinations administered on 17-Aug-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), a dose of pneumococcal 4 6B 9V 14 18C 19F 23F conj vaccine (CRM197) (PREVNAR) and a dose of poliovirus vaccine inactivated (IPOL). On 28-Sep-2006 the patient developed vomiting and irritability. The patient was subsequently hospitalized due to persistent vomiting. While hospitalized intussusception was diagnosed and reduced via Barium enema. The patient recovered within 24 hours and was discharged to home. At the time of the report the patient was noted to be doing fine by the physician. The physician indicated that he would provide additional information, including medical records if it became available. No product quality comp


Changed on 5/13/2013

VAERS ID: 268712 Before After
VAERS Form:
Age:0.2
Gender:Male
Location:Washington
Vaccinated:2006-08-17
Onset:2006-09-28
Submitted:2006-12-08
Entered:2006-12-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (NO BRAND NAME) / UNKNOWN MANUFACTURER - / - - / -
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. - / - - / -
HIBV: HIB (ACTHIB) / AVENTIS PASTEUR - / - - / -
ROTHB5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0146F / 2 - / PO
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0146F / 2 - / PO

Administered by: Other      Purchased by: Other
Symptoms: Intussusception, Irritability, Pyrexia, Viral infection, Vomiting

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 1     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: 8/2/06 X Ray normal, diagnostic lab normal, body temp fever.
CDC 'Split Type': WAES0612USA00126

Write-up: Information has been received from a physician concerning a 23 week old male, with no significant medical history, who, on 16-Jun-2006 was vaccinated with an oral, 2.0 ml, first dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine) (Lot#653661/0146F). Concomitant vaccination administered on 16-Jun-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), and a dose if hepatitis B virus vaccine rHBsAg (yeast). On 14-Jul-2006 the patient was vaccinated with a second 2.0 ml oral dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine). There were no concomitant vaccinations given on 14-Jul-2006. In July 2006 the patient was noted to have fallen out of a shopping cart. On 02-Aug-2006 the patient developed a fever. The patient was taken to the emergency room where an x-ray and labs (not further specified) were normal. No formal diagnosis was made and the patient was simply thought to have a virus. On 17-Aug-2006 the patient was vaccinated with a third 2.0 ml oral dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine). Concomitant vaccinations administered on 17-Aug-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), a dose of pneumococcal 4 6B 9V 14 18C 19F 23F conj vaccine (CRM197) (PREVNAR) and a dose of poliovirus vaccine inactivated (IPOL). On 28-Sep-2006 the patient developed vomiting and irritability. The patient was subsequently hospitalized due to persistent vomiting. While hospitalized intussusception was diagnosed and reduced via Barium enema. The patient recovered within 24 hours and was discharged to home. At the time of the report the patient was noted to be doing fine by the physician. The physician indicated that he would provide additional information, including medical records if it became available. No product quality comp


Changed on 3/14/2014

VAERS ID: 268712 Before After
VAERS Form:
Age:0.2 0.3
Gender:Male
Location:Washington
Vaccinated:2006-08-17
Onset:2006-09-28
Submitted:2006-12-08
Entered:2006-12-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (NO BRAND NAME) DTAP (DAPTACEL) / UNKNOWN MANUFACTURER SANOFI PASTEUR - / - - UN / - UN
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. - / - - UN / - UN
HIBV: HIB (ACTHIB) / AVENTIS PASTEUR SANOFI PASTEUR - / - - UN / - UN
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0146F / 2 - / PO

Administered by: Other      Purchased by: Other
Symptoms: Intussusception, Irritability, Pyrexia, Viral infection, Vomiting

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 1     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: 8/2/06 X Ray normal, diagnostic lab normal, body temp fever.
CDC 'Split Type': WAES0612USA00126

Write-up: Information has been received from a physician concerning a 23 week old male, with no significant medical history, who, on 16-Jun-2006 was vaccinated with an oral, 2.0 ml, first dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine) (Lot#653661/0146F). Concomitant vaccination administered on 16-Jun-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), and a dose if hepatitis B virus vaccine rHBsAg (yeast). On 14-Jul-2006 the patient was vaccinated with a second 2.0 ml oral dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine). There were no concomitant vaccinations given on 14-Jul-2006. In July 2006 the patient was noted to have fallen out of a shopping cart. On 02-Aug-2006 the patient developed a fever. The patient was taken to the emergency room where an x-ray and labs (not further specified) were normal. No formal diagnosis was made and the patient was simply thought to have a virus. On 17-Aug-2006 the patient was vaccinated with a third 2.0 ml oral dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine). Concomitant vaccinations administered on 17-Aug-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), a dose of pneumococcal 4 6B 9V 14 18C 19F 23F conj vaccine (CRM197) (PREVNAR) and a dose of poliovirus vaccine inactivated (IPOL). On 28-Sep-2006 the patient developed vomiting and irritability. The patient was subsequently hospitalized due to persistent vomiting. While hospitalized intussusception was diagnosed and reduced via Barium enema. The patient recovered within 24 hours and was discharged to home. At the time of the report the patient was noted to be doing fine by the physician. The physician indicated that he would provide additional information, including medical records if it became available. No product quality comp complaint was involved. No other information was provided. Additional information has been requested.


Changed on 2/14/2017

VAERS ID: 268712 Before After
VAERS Form:
Age:0.3 0.34
Gender:Male
Location:Washington
Vaccinated:2006-08-17
Onset:2006-09-28
Submitted:2006-12-08
Entered:2006-12-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (DAPTACEL) / SANOFI PASTEUR - / - UN / UN
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. - / - UN / UN
HIBV: HIB (ACTHIB) / SANOFI PASTEUR - / - UN / UN
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0146F / 2 - / PO

Administered by: Other      Purchased by: Other
Symptoms: Intussusception, Irritability, Pyrexia, Viral infection, Vomiting

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 1     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: 8/2/06 X Ray normal, diagnostic lab normal, body temp fever.
CDC 'Split Type': WAES0612USA00126

Write-up: Information has been received from a physician concerning a 23 week old male, with no significant medical history, who, on 16-Jun-2006 was vaccinated with an oral, 2.0 ml, first dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine) (Lot#653661/0146F). Concomitant vaccination administered on 16-Jun-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), and a dose if hepatitis B virus vaccine rHBsAg (yeast). On 14-Jul-2006 the patient was vaccinated with a second 2.0 ml oral dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine). There were no concomitant vaccinations given on 14-Jul-2006. In July 2006 the patient was noted to have fallen out of a shopping cart. On 02-Aug-2006 the patient developed a fever. The patient was taken to the emergency room where an x-ray and labs (not further specified) were normal. No formal diagnosis was made and the patient was simply thought to have a virus. On 17-Aug-2006 the patient was vaccinated with a third 2.0 ml oral dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine). Concomitant vaccinations administered on 17-Aug-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), a dose of pneumococcal 4 6B 9V 14 18C 19F 23F conj vaccine (CRM197) (PREVNAR) and a dose of poliovirus vaccine inactivated (IPOL). On 28-Sep-2006 the patient developed vomiting and irritability. The patient was subsequently hospitalized due to persistent vomiting. While hospitalized intussusception was diagnosed and reduced via Barium enema. The patient recovered within 24 hours and was discharged to home. At the time of the report the patient was noted to be doing fine by the physician. The physician indicated that he would provide additional information, including medical records if it became available. No product quality complaint was involved. No other information was provided. Additional information has been requested.


Changed on 9/14/2017

VAERS ID: 268712 Before After
VAERS Form:(blank) 1
Age:0.34
Gender:Male
Location:Washington
Vaccinated:2006-08-17
Onset:2006-09-28
Submitted:2006-12-08
Entered:2006-12-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (DAPTACEL) / SANOFI PASTEUR - / - UNK UN / UN
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. - / - UNK UN / UN
HIBV: HIB (ACTHIB) / SANOFI PASTEUR - / - UNK UN / UN
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0146F / 2 3 - MO / PO

Administered by: Other      Purchased by: Other
Symptoms: Intussusception, Irritability, Pyrexia, Viral infection, Vomiting

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 1     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: 8/2/06 X Ray normal, diagnostic lab normal, body temp fever.
CDC 'Split Type': WAES0612USA00126

Write-up: Information has been received from a physician concerning a 23 week old male, with no significant medical history, who, on 16-Jun-2006 was vaccinated with an oral, 2.0 ml, first dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine) (Lot#653661/0146F). Concomitant vaccination administered on 16-Jun-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), and a dose if hepatitis B virus vaccine rHBsAg (yeast). On 14-Jul-2006 the patient was vaccinated with a second 2.0 ml oral dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine). There were no concomitant vaccinations given on 14-Jul-2006. In July 2006 the patient was noted to have fallen out of a shopping cart. On 02-Aug-2006 the patient developed a fever. The patient was taken to the emergency room where an x-ray and labs (not further specified) were normal. No formal diagnosis was made and the patient was simply thought to have a virus. On 17-Aug-2006 the patient was vaccinated with a third 2.0 ml oral dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine). Concomitant vaccinations administered on 17-Aug-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), a dose of pneumococcal 4 6B 9V 14 18C 19F 23F conj vaccine (CRM197) (PREVNAR) and a dose of poliovirus vaccine inactivated (IPOL). On 28-Sep-2006 the patient developed vomiting and irritability. The patient was subsequently hospitalized due to persistent vomiting. While hospitalized intussusception was diagnosed and reduced via Barium enema. The patient recovered within 24 hours and was discharged to home. At the time of the report the patient was noted to be doing fine by the physician. The physician indicated that he would provide additional information, including medical records if it became available. No product quality complaint was involved. No other information was provided. Additional information has been requested.


Changed on 2/14/2018

VAERS ID: 268712 Before After
VAERS Form:1
Age:0.34
Gender:Male
Location:Washington
Vaccinated:2006-08-17
Onset:2006-09-28
Submitted:2006-12-08
Entered:2006-12-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (DAPTACEL) / SANOFI PASTEUR - / UNK UN / UN
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. - / UNK UN / UN
HIBV: HIB (ACTHIB) / SANOFI PASTEUR - / UNK UN / UN
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0146F / 3 MO / PO

Administered by: Other      Purchased by: Other
Symptoms: Intussusception, Irritability, Pyrexia, Viral infection, Vomiting

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? Yes
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 1     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: 8/2/06 X Ray normal, diagnostic lab normal, body temp fever.
CDC 'Split Type': WAES0612USA00126

Write-up: Information has been received from a physician concerning a 23 week old male, with no significant medical history, who, on 16-Jun-2006 was vaccinated with an oral, 2.0 ml, first dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine) (Lot#653661/0146F). Concomitant vaccination administered on 16-Jun-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), and a dose if hepatitis B virus vaccine rHBsAg (yeast). On 14-Jul-2006 the patient was vaccinated with a second 2.0 ml oral dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine). There were no concomitant vaccinations given on 14-Jul-2006. In July 2006 the patient was noted to have fallen out of a shopping cart. On 02-Aug-2006 the patient developed a fever. The patient was taken to the emergency room where an x-ray and labs (not further specified) were normal. No formal diagnosis was made and the patient was simply thought to have a virus. On 17-Aug-2006 the patient was vaccinated with a third 2.0 ml oral dose of rotavirus G1 G2 G3 G4 P1 reassortant vaccine live (human-bovine). Concomitant vaccinations administered on 17-Aug-2006 included a dose of diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid, a dose of Hib conj vaccine (tetanus toxoid) (ACTHIB), a dose of pneumococcal 4 6B 9V 14 18C 19F 23F conj vaccine (CRM197) (PREVNAR) and a dose of poliovirus vaccine inactivated (IPOL). On 28-Sep-2006 the patient developed vomiting and irritability. The patient was subsequently hospitalized due to persistent vomiting. While hospitalized intussusception was diagnosed and reduced via Barium enema. The patient recovered within 24 hours and was discharged to home. At the time of the report the patient was noted to be doing fine by the physician. The physician indicated that he would provide additional information, including medical records if it became available. No product quality complaint was involved. No other information was provided. Additional information has been requested.


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