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This is VAERS ID 293964

History of Changes from the VAERS Wayback Machine

First Appeared on 12/31/2007

VAERS ID: 293964
VAERS Form:
Age:0.2
Gender:Male
Location:Florida
Vaccinated:2007-08-29
Onset:2007-09-06
Submitted:2007-10-19
Entered:2007-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHE: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B115AA / 0 RL / -
HIBV: HIB (ACTHIB) / SANOFI PASTEUR UF120AA / 0 LL / -
PNC: PNEUMO (PREVNAR) / WYETH PHARMACEUTICALS, INC B08679K / 0 LL / -
ROTHB5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0169U / 0 - / PO

Administered by: Other      Purchased by: Unknown
Symptoms: Barium enema, Crying, Diarrhoea, Intussusception, Enema administration

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? Yes, days: 2     Extended hospital stay? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type':

Write-up: Information has been received from a physician concerning an 8 week old male who received his first dose of oral Rotateq. On an unspecified date, he was seen in the physician''''s office after he had developed sudden bouts of crying and appeared to be in pa"in. At the time of this report, the physician was awaiting the results of unspecified test but he suspects a diagnosis of intussusception. It is reported that the patient has not recovered. A product quality complaint was not reported. No further informat


Changed on 12/8/2009

VAERS ID: 293964 Before After
VAERS Form:
Age:0.2
Gender:Male
Location:Florida
Vaccinated:2007-08-29
Onset:2007-09-06
Submitted:2007-10-19
Entered:2007-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHE: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B115AA / 0 RL / -
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B115AA / 0 RL / -
HIBV: HIB (ACTHIB) / SANOFI PASTEUR UF120AA / 0 LL / -
PNC: PNEUMO (PREVNAR) / WYETH PHARMACEUTICALS, INC B08679K / 0 LL / -
ROTHB5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0169U / 0 - / PO

Administered by: Other      Purchased by: Unknown Other
Symptoms: Barium enema, Crying, Diarrhoea, Intussusception, Irritability, Pain, Urinary system X-ray, Vomiting, Enema administration, Ultrasound abdomen abnormal, Oral intake reduced

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? Yes, days: 2     Extended hospital stay? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': (blank) WAES0710USA02633

Write-up: Information has been received from a physician concerning an 8 week old male who received his first dose of oral Rotateq. On an unspecified date, he was seen in the physician''''s physician''s office after he had developed sudden bouts of crying and appeared to be in pa"in. pain. At the time of this report, the physician was awaiting the results of unspecified test but he suspects a diagnosis of intussusception. It is reported that the patient has not recovered. A product quality complaint was not reported. No further informat information was available. Upon internal review it was determined that intussusception was an other important medical event. Additional information has been requested. 10/23/07 Patient demographics provided by CDC./ss 10/23/2007 Reviewed hospital medical records which reveal patient experienced emesis x 2, diarrhea, irritability, decreased oral intake x 1 week. Seen by pcp & KUB obtained c/w IS. Confirmed by BE as outpatient & sent to outlying hospital but they were unable to do the BE for reduction. Transferred to higher level of care. Repeat KUB revealed distended bowel but no IS. Admitted 9/7-9/8/07 for observation s/p reduction. Had recurrent IS s/s. US of abdomen confirmed IS within transverse colon recurred & air contrast enema successfully reduced. Surgical consult done. FINAL DX: Intussusception, enema reduced. Records faxed to CDC. 11/30/07 Reviewed hospital ER records which reveal patient seen 9/6/07 with intermittent emesis, watery stools & poor appetite x 4 days. BE revealed IS & patient transferred to higher level of care. Records faxed to CDC.


Changed on 3/2/2010

VAERS ID: 293964 Before After
VAERS Form:
Age:0.2
Gender:Male
Location:Florida
Vaccinated:2007-08-29
Onset:2007-09-06
Submitted:2007-10-19
Entered:2007-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B115AA / 0 RL / -
HIBV: HIB (ACTHIB) / SANOFI PASTEUR UF120AA / 0 LL / -
PNC: PNEUMO (PREVNAR) PNEUMO (PREVNAR7) / WYETH PHARMACEUTICALS, INC B08679K / 0 LL / -
ROTHB5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0169U / 0 - / PO

Administered by: Other      Purchased by: Other
Symptoms: Barium enema, Crying, Diarrhoea, Intussusception, Irritability, Pain, Urinary system X-ray, Vomiting, Enema administration, Ultrasound abdomen abnormal, Oral intake reduced

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? Yes, days: 2     Extended hospital stay? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0710USA02633

Write-up: Information has been received from a physician concerning an 8 week old male who received his first dose of oral Rotateq. On an unspecified date, he was seen in the physician''s office after he had developed sudden bouts of crying and appeared to be in pain. At the time of this report, the physician was awaiting the results of unspecified test but he suspects a diagnosis of intussusception. It is reported that the patient has not recovered. A product quality complaint was not reported. No further information was available. Upon internal review it was determined that intussusception was an other important medical event. Additional information has been requested. 10/23/07 Patient demographics provided by CDC./ss 10/23/2007 Reviewed hospital medical records which reveal patient experienced emesis x 2, diarrhea, irritability, decreased oral intake x 1 week. Seen by pcp & KUB obtained c/w IS. Confirmed by BE as outpatient & sent to outlying hospital but they were unable to do the BE for reduction. Transferred to higher level of care. Repeat KUB revealed distended bowel but no IS. Admitted 9/7-9/8/07 for observation s/p reduction. Had recurrent IS s/s. US of abdomen confirmed IS within transverse colon recurred & air contrast enema successfully reduced. Surgical consult done. FINAL DX: Intussusception, enema reduced. Records faxed to CDC. 11/30/07 Reviewed hospital ER records which reveal patient seen 9/6/07 with intermittent emesis, watery stools & poor appetite x 4 days. BE revealed IS & patient transferred to higher level of care. Records faxed to CDC.


Changed on 4/7/2010

VAERS ID: 293964 Before After
VAERS Form:
Age:0.2
Gender:Male
Location:Florida
Vaccinated:2007-08-29
Onset:2007-09-06
Submitted:2007-10-19
Entered:2007-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B115AA / 0 RL / -
HIBV: HIB (ACTHIB) / SANOFI PASTEUR UF120AA / 0 LL / -
PNC: PNEUMO (PREVNAR7) PNEUMO (PREVNAR) / WYETH PHARMACEUTICALS, INC B08679K / 0 LL / -
ROTHB5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0169U / 0 - / PO

Administered by: Other      Purchased by: Other
Symptoms: Barium enema, Crying, Diarrhoea, Intussusception, Irritability, Pain, Urinary system X-ray, Vomiting, Enema administration, Ultrasound abdomen abnormal, Oral intake reduced

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? Yes, days: 2     Extended hospital stay? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0710USA02633

Write-up: Information has been received from a physician concerning an 8 week old male who received his first dose of oral Rotateq. On an unspecified date, he was seen in the physician''s office after he had developed sudden bouts of crying and appeared to be in pain. At the time of this report, the physician was awaiting the results of unspecified test but he suspects a diagnosis of intussusception. It is reported that the patient has not recovered. A product quality complaint was not reported. No further information was available. Upon internal review it was determined that intussusception was an other important medical event. Additional information has been requested. 10/23/07 Patient demographics provided by CDC./ss 10/23/2007 Reviewed hospital medical records which reveal patient experienced emesis x 2, diarrhea, irritability, decreased oral intake x 1 week. Seen by pcp & KUB obtained c/w IS. Confirmed by BE as outpatient & sent to outlying hospital but they were unable to do the BE for reduction. Transferred to higher level of care. Repeat KUB revealed distended bowel but no IS. Admitted 9/7-9/8/07 for observation s/p reduction. Had recurrent IS s/s. US of abdomen confirmed IS within transverse colon recurred & air contrast enema successfully reduced. Surgical consult done. FINAL DX: Intussusception, enema reduced. Records faxed to CDC. 11/30/07 Reviewed hospital ER records which reveal patient seen 9/6/07 with intermittent emesis, watery stools & poor appetite x 4 days. BE revealed IS & patient transferred to higher level of care. Records faxed to CDC.


Changed on 8/31/2010

VAERS ID: 293964 Before After
VAERS Form:
Age:0.2
Gender:Male
Location:Florida
Vaccinated:2007-08-29
Onset:2007-09-06
Submitted:2007-10-19
Entered:2007-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B115AA / 0 RL / -
HIBV: HIB (ACTHIB) / SANOFI PASTEUR UF120AA / 0 LL / -
PNC: PNEUMO (PREVNAR) / WYETH PHARMACEUTICALS, INC PFIZER/WYETH B08679K / 0 LL / -
ROTHB5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0169U / 0 - / PO

Administered by: Other      Purchased by: Other
Symptoms: Barium enema, Crying, Diarrhoea, Intussusception, Irritability, Pain, Urinary system X-ray, Vomiting, Enema administration, Ultrasound abdomen abnormal, Oral intake reduced

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? Yes, days: 2     Extended hospital stay? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0710USA02633

Write-up: Information has been received from a physician concerning an 8 week old male who received his first dose of oral Rotateq. On an unspecified date, he was seen in the physician''s office after he had developed sudden bouts of crying and appeared to be in pain. At the time of this report, the physician was awaiting the results of unspecified test but he suspects a diagnosis of intussusception. It is reported that the patient has not recovered. A product quality complaint was not reported. No further information was available. Upon internal review it was determined that intussusception was an other important medical event. Additional information has been requested. 10/23/07 Patient demographics provided by CDC./ss 10/23/2007 Reviewed hospital medical records which reveal patient experienced emesis x 2, diarrhea, irritability, decreased oral intake x 1 week. Seen by pcp & KUB obtained c/w IS. Confirmed by BE as outpatient & sent to outlying hospital but they were unable to do the BE for reduction. Transferred to higher level of care. Repeat KUB revealed distended bowel but no IS. Admitted 9/7-9/8/07 for observation s/p reduction. Had recurrent IS s/s. US of abdomen confirmed IS within transverse colon recurred & air contrast enema successfully reduced. Surgical consult done. FINAL DX: Intussusception, enema reduced. Records faxed to CDC. 11/30/07 Reviewed hospital ER records which reveal patient seen 9/6/07 with intermittent emesis, watery stools & poor appetite x 4 days. BE revealed IS & patient transferred to higher level of care. Records faxed to CDC.


Changed on 5/13/2013

VAERS ID: 293964 Before After
VAERS Form:
Age:0.2
Gender:Male
Location:Florida
Vaccinated:2007-08-29
Onset:2007-09-06
Submitted:2007-10-19
Entered:2007-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B115AA / 0 RL / -
HIBV: HIB (ACTHIB) / SANOFI PASTEUR UF120AA / 0 LL / -
PNC: PNEUMO (PREVNAR) / PFIZER/WYETH B08679K / 0 LL / -
ROTHB5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0169U / 0 - / PO
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0169U / 0 - / PO

Administered by: Other      Purchased by: Other
Symptoms: Barium enema, Crying, Diarrhoea, Intussusception, Irritability, Pain, Urinary system X-ray, Vomiting, Enema administration, Ultrasound abdomen abnormal, Oral intake reduced

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? Yes, days: 2     Extended hospital stay? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0710USA02633

Write-up: Information has been received from a physician concerning an 8 week old male who received his first dose of oral Rotateq. On an unspecified date, he was seen in the physician''s office after he had developed sudden bouts of crying and appeared to be in pain. At the time of this report, the physician was awaiting the results of unspecified test but he suspects a diagnosis of intussusception. It is reported that the patient has not recovered. A product quality complaint was not reported. No further information was available. Upon internal review it was determined that intussusception was an other important medical event. Additional information has been requested. 10/23/07 Patient demographics provided by CDC./ss 10/23/2007 Reviewed hospital medical records which reveal patient experienced emesis x 2, diarrhea, irritability, decreased oral intake x 1 week. Seen by pcp & KUB obtained c/w IS. Confirmed by BE as outpatient & sent to outlying hospital but they were unable to do the BE for reduction. Transferred to higher level of care. Repeat KUB revealed distended bowel but no IS. Admitted 9/7-9/8/07 for observation s/p reduction. Had recurrent IS s/s. US of abdomen confirmed IS within transverse colon recurred & air contrast enema successfully reduced. Surgical consult done. FINAL DX: Intussusception, enema reduced. Records faxed to CDC. 11/30/07 Reviewed hospital ER records which reveal patient seen 9/6/07 with intermittent emesis, watery stools & poor appetite x 4 days. BE revealed IS & patient transferred to higher level of care. Records faxed to CDC.


Changed on 4/14/2017

VAERS ID: 293964 Before After
VAERS Form:
Age:0.2
Gender:Male
Location:Florida
Vaccinated:2007-08-29
Onset:2007-09-06
Submitted:2007-10-19
Entered:2007-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B115AA / 0 RL / -
HIBV: HIB (ACTHIB) / SANOFI PASTEUR UF120AA / 0 LL / -
PNC: PNEUMO (PREVNAR) / PFIZER/WYETH B08679K / 0 LL / -
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0169U / 0 - / PO

Administered by: Other      Purchased by: Other
Symptoms: Barium enema, Crying, Diarrhoea, Intussusception, Irritability, Pain, Urinary system X-ray, Vomiting, Enema administration, Ultrasound abdomen abnormal, Oral intake reduced

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? Yes, days: 2     Extended hospital stay? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0710USA02633

Write-up: Information has been received from a physician concerning an 8 week old male who received his first dose of oral Rotateq. On an unspecified date, he was seen in the physician''s office after he had developed sudden bouts of crying and appeared to be in pain. At the time of this report, the physician was awaiting the results of unspecified test but he suspects a diagnosis of intussusception. It is reported that the patient has not recovered. A product quality complaint was not reported. No further information was available. Upon internal review it was determined that intussusception was an other important medical event. Additional information has been requested. 10/23/07 Patient demographics provided by CDC./ss 10/23/2007 Reviewed hospital medical records which reveal patient experienced emesis x 2, diarrhea, irritability, decreased oral intake x 1 week. Seen by pcp & KUB obtained c/w IS. Confirmed by BE as outpatient & sent to outlying hospital but they were unable to do the BE for reduction. Transferred to higher level of care. Repeat KUB revealed distended bowel but no IS. Admitted 9/7-9/8/07 for observation s/p reduction. Had recurrent IS s/s. US of abdomen confirmed IS within transverse colon recurred & air contrast enema successfully reduced. Surgical consult done. FINAL DX: Intussusception, enema reduced. Records faxed to CDC. 11/30/07 Reviewed hospital ER records which reveal patient seen 9/6/07 with intermittent emesis, watery stools & poor appetite x 4 days. BE revealed IS & patient transferred to higher level of care. Records faxed to CDC.


Changed on 9/14/2017

VAERS ID: 293964 Before After
VAERS Form:(blank) 1
Age:0.2
Gender:Male
Location:Florida
Vaccinated:2007-08-29
Onset:2007-09-06
Submitted:2007-10-19
Entered:2007-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B115AA / 0 1 RL / -
HIBV: HIB (ACTHIB) / SANOFI PASTEUR UF120AA / 0 1 LL / -
PNC: PNEUMO (PREVNAR) / PFIZER/WYETH B08679K / 0 1 LL / -
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0169U / 0 1 - MO / PO

Administered by: Other      Purchased by: Other
Symptoms: Crying, Intussusception, Pain

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? Yes, days: 2     Extended hospital stay? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0710USA02633

Write-up: Information has been received from a physician concerning an 8 week old male who received his first dose of oral Rotateq. On an unspecified date, he was seen in the physician''s office after he had developed sudden bouts of crying and appeared to be in pain. At the time of this report, the physician was awaiting the results of unspecified test but he suspects a diagnosis of intussusception. It is reported that the patient has not recovered. A product quality complaint was not reported. No further information was available. Upon internal review it was determined that intussusception was an other important medical event. Additional information has been requested. 10/23/07 Patient demographics provided by CDC./ss 10/23/2007 Reviewed hospital medical records which reveal patient experienced emesis x 2, diarrhea, irritability, decreased oral intake x 1 week. Seen by pcp & KUB obtained c/w IS. Confirmed by BE as outpatient & sent to outlying hospital but they were unable to do the BE for reduction. Transferred to higher level of care. Repeat KUB revealed distended bowel but no IS. Admitted 9/7-9/8/07 for observation s/p reduction. Had recurrent IS s/s. US of abdomen confirmed IS within transverse colon recurred & air contrast enema successfully reduced. Surgical consult done. FINAL DX: Intussusception, enema reduced. Records faxed to CDC. 11/30/07 Reviewed hospital ER records which reveal patient seen 9/6/07 with intermittent emesis, watery stools & poor appetite x 4 days. BE revealed IS & patient transferred to higher level of care. Records faxed to CDC.


Changed on 2/14/2018

VAERS ID: 293964 Before After
VAERS Form:1
Age:0.2
Gender:Male
Location:Florida
Vaccinated:2007-08-29
Onset:2007-09-06
Submitted:2007-10-19
Entered:2007-10-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B115AA / 1 RL / -
HIBV: HIB (ACTHIB) / SANOFI PASTEUR UF120AA / 1 LL / -
PNC: PNEUMO (PREVNAR) / PFIZER/WYETH B08679K / 1 LL / -
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 0169U / 1 MO / PO

Administered by: Other      Purchased by: Other
Symptoms: Crying, Intussusception, Pain

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? Yes, days: 2     Extended hospital stay? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0710USA02633

Write-up: Information has been received from a physician concerning an 8 week old male who received his first dose of oral Rotateq. On an unspecified date, he was seen in the physician''s office after he had developed sudden bouts of crying and appeared to be in pain. At the time of this report, the physician was awaiting the results of unspecified test but he suspects a diagnosis of intussusception. It is reported that the patient has not recovered. A product quality complaint was not reported. No further information was available. Upon internal review it was determined that intussusception was an other important medical event. Additional information has been requested. 10/23/07 Patient demographics provided by CDC./ss 10/23/2007 Reviewed hospital medical records which reveal patient experienced emesis x 2, diarrhea, irritability, decreased oral intake x 1 week. Seen by pcp & KUB obtained c/w IS. Confirmed by BE as outpatient & sent to outlying hospital but they were unable to do the BE for reduction. Transferred to higher level of care. Repeat KUB revealed distended bowel but no IS. Admitted 9/7-9/8/07 for observation s/p reduction. Had recurrent IS s/s. US of abdomen confirmed IS within transverse colon recurred & air contrast enema successfully reduced. Surgical consult done. FINAL DX: Intussusception, enema reduced. Records faxed to CDC. 11/30/07 Reviewed hospital ER records which reveal patient seen 9/6/07 with intermittent emesis, watery stools & poor appetite x 4 days. BE revealed IS & patient transferred to higher level of care. Records faxed to CDC.


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