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Found 1007 cases where Vaccine is RVX

Table

   
AgeCountPercent
< 3 Years87186.49%
3-6 Years50.5%
9-12 Years10.1%
44-65 Years10.1%
Unknown12912.81%
TOTAL1007100%

Case Details

This is page 1 out of 101

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VAERS ID: 264479 (history)  
Form: Version 1.0  
Age: 0.17  
Gender: Female  
Location: Unknown  
Vaccinated:2006-07-11
Onset:2006-07-20
   Days after vaccination:9
Submitted: 2006-10-10
   Days after onset:82
Entered: 2006-10-13
   Days after submission:3
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 UN / IM
HIBV: HIB (ACTHIB) / SANOFI PASTEUR - / 1 UN / IM
PNC: PNEUMO (PREVNAR) / PFIZER/WYETH - / 1 UN / IM
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 1 MO / PO

Administered by: Unknown       Purchased by: Unknown
Symptoms: Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

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, 3 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Lansoprazole
Current Illness:
Preexisting Conditions: The subject had a medical history of gastrointestinal reflux disease, which started on 6/29/06 and continued at the time of reporting.
Allergies:
Diagnostic Lab Data:
CDC Split Type: 200602568

Write-up: Initial information received on 9/29/06 from another company regarding a subject who was enrolled in a clinical trial sponsored by the other company. A two month old female subject was enrolled in the prophylactic open study 10531. On 7/11/06, the subject received initial doses of the following vaccine, ActHib, Pediarix, and Prevnar. The vaccine were administered intra muscularly in the thigh. The subject also received a dose of Rotavirus vaccine, administered per OS on the same date. The lot numbers were not reported for any of the vaccines. The subject had a history of gastrointestinal reflux disease, which started on 6/29/06 and continued at the time of reporting. On 7/20/06, nine days after the first dosed of Rotavirus vaccine, ActHib, Pediarix and Prevnar, and 20 days after the last dose of lansoprazole, the subject developed a fever of unk origin (temp of 38.9 deg C) and was hospitalized. Relevant tests on 7/20/06 included a lumbar puncture, as well as blood and urine cultures. The lumbar puncture was negative and all cultures were neg. No details of relevant assessments were available. The subject was treated with paracetamol, ampicillin trihydrate, ceftriaxone sodium and cefotaxime. The subject was discharged from the hospital on 7/22/06. The investigator considered that there was a reasonable possibility that the fever may have been caused by rotavirus vaccine, Pediarix, ActHib and Prevnar, and that the event was possibly due to the concomitant medication with lansoprazole and the subjects medical condition of gastroesophageal reflux disease, the investigator also replied that although it is possible the childs fever was due to the rotavirus vaccine, he believes that the possibility is quite small and more likely attributable to a viral syndrome.


VAERS ID: 265890 (history)  
Form: Version 1.0  
Age: 0.15  
Gender: Male  
Location: Ohio  
Vaccinated:2006-11-01
Onset:2006-11-01
   Days after vaccination:0
Submitted: 2006-11-02
   Days after onset:1
Entered: 2006-11-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (TRIPEDIA) / SANOFI PASTEUR U1965BA / 1 LL / IM
HBHEPB: HIB + HEP B (COMVAX) / MERCK & CO. INC. 0012F / 1 RL / IM
IPV: POLIO VIRUS, INACT. (IPOL) / SANOFI PASTEUR Y1032 / 1 LL / IM
PNC: PNEUMO (PREVNAR) / PFIZER/WYETH B08683C / 1 RL / IM
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER 01457 / 1 MO / PO

Administered by: Unknown       Purchased by: Unknown
Symptoms: Body temperature increased, Condition aggravated, Pallor
SMQs:, Neuroleptic malignant syndrome (broad), Hypotonic-hyporesponsive episode (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: none
Current Illness: None
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data: CBC negative, Cath U/A negative. CSF negative. Cultures pending as of 11-02-2006 12:45PM Urine culture negative, blood culture negative, CSF colorless, clear, gram stain negative. CSF protein 49.5, glucose 53, neut 20, lymph 60, mono/mac 20, WBC 8 RBC 380.
CDC Split Type:

Write-up: Recieved DaPT, IPV, Comvax, Prevnar and Rototeq at 11:30AM 11-01-2006. at 7:20PM had a episode of pallor. Parents called squad, arrived at 5 minutes into the episode. Was still pale. Transferred to hospital. Pallor had resolved by arrival, BP was 78/palp. Temp 38.1. Rule out sepsis work up initiated. CBC was negative, Cath U/A negative, CSF was clear(Cultures all pending). Patient admitted. Had another spell overnight (2 minutes per mother) DC Summary received for DOS 11/2/06-DC DX: Post immunization reaction. Became pale, episode of pallor and spike temp of 38.1. No vomiting, no diarrhea.


VAERS ID: 269418 (history)  
Form: Version 1.0  
Age: 0.12  
Gender: Female  
Location: Michigan  
Vaccinated:2006-11-28
Onset:2006-12-05
   Days after vaccination:7
Submitted: 2006-12-19
   Days after onset:14
Entered: 2006-12-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER XXXXX / UNK MO / PO

Administered by: Unknown       Purchased by: Unknown
Symptoms: Haematochezia
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Gastrointestinal haemorrhage (narrow), Ischaemic colitis (broad)

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

Write-up: 7days after rotavirus, had bloody, mucousy stools.


VAERS ID: 270217 (history)  
Form: Version 1.0  
Age: 0.18  
Gender: Male  
Location: California  
Vaccinated:2006-12-14
Onset:2006-12-14
   Days after vaccination:0
Submitted: 2007-01-08
   Days after onset:25
Entered: 2007-01-09
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK - / -

Administered by: Public       Purchased by: Public
Symptoms: Choking, Cyanosis, Depressed level of consciousness, Respiratory rate decreased
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypersensitivity (broad), Respiratory failure (narrow), Hypoglycaemia (broad)

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: NONE
Current Illness: NONE
Preexisting Conditions: NONE
Allergies:
Diagnostic Lab Data: NONE
CDC Split Type:

Write-up: 9 week old male given rotavirus IZ. 1st IZ (before any shots). Child immediately had decrease respiration and transient cyanosis and 5-10 mild decreased LOX. Looked stunned. No intervention NO O2, simple stimulation and holding, then fine other IZA given next day. Prof simple choking but did not have typical choking symptoms.


VAERS ID: 270956 (history)  
Form: Version 1.0  
Age: 0.2  
Gender: Female  
Location: Pennsylvania  
Vaccinated:2007-01-18
Onset:2007-01-20
   Days after vaccination:2
Submitted: 2007-01-22
   Days after onset:2
Entered: 2007-01-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HIBV: HIB (PEDVAXHIB) / MERCK & CO. INC. 1015F / 1 LL / IM
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER MERCK 1111F / UNK MO / PO

Administered by: Private       Purchased by: Private
Symptoms: Dermatitis diaper, Diarrhoea
SMQs:, Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: zantac
Current Illness: no
Preexisting Conditions: gastroesophageal reflux, fussy baby
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: severe diarrhea and diaper rash 2 days following administration of the vaccine


VAERS ID: 271922 (history)  
Form: Version 1.0  
Age: 0.2  
Gender: Female  
Location: Missouri  
Vaccinated:2007-01-26
Onset:2007-02-04
   Days after vaccination:9
Submitted: 2007-02-07
   Days after onset:3
Entered: 2007-02-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEP: HEP B (NO BRAND NAME) / UNKNOWN MANUFACTURER UNKNOWN / 1 UN / IM
IPV: POLIO VIRUS, INACT. (NO BRAND NAME) / UNKNOWN MANUFACTURER UNKNOWN / 1 UN / IM
PNC: PNEUMO (PREVNAR) / PFIZER/WYETH UNKNOWN / 1 UN / ID
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER UNKNOWN / 1 MO / PO

Administered by: Private       Purchased by: Unknown
Symptoms: Haematochezia
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Gastrointestinal haemorrhage (narrow), Ischaemic colitis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: None
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data: Blood in stool seen by physician
CDC Split Type:

Write-up: Blood in stool 8 days after first Rotavaccine


VAERS ID: 272226 (history)  
Form: Version 1.0  
Age: 1.51  
Gender: Female  
Location: Indiana  
Vaccinated:2007-02-12
Onset:2007-02-13
   Days after vaccination:1
Submitted: 2007-02-14
   Days after onset:1
Entered: 2007-02-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK LL / IM
HEPA: HEP A (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK RL / IM
HIBV: HIB (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK LL / IM
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER 14639 / UNK UN / UN

Administered by: Unknown       Purchased by: Unknown
Symptoms: Diarrhoea, Influenza like illness, Pyrexia, Viral infection, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

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:
Current Illness: Cold (runny nose, cough); teething
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: After receiving the DTaP, the Hepatitis A, and the Hib vaccines, patient experienced extreme vomiting (12 times in 24 hours) and diarrhea. She had a fever of 103.3 F. Prior to the vaccine she had cold symptoms (runny nose, cough) and was bringing in a tooth, but she exhibited NO stomach flu-like symptoms until after she''d received the vaccines. We thought it might be a virus, but neither her father nor I got sick, in spite of having repeated and prolonged contact with patient''s bodily fluids (snot, vomit, etc.) as is the case when a toddler is so ill.


VAERS ID: 272461 (history)  
Form: Version 1.0  
Age: 0.13  
Gender: Female  
Location: California  
Vaccinated:2007-02-02
Onset:2007-02-03
   Days after vaccination:1
Submitted: 2007-02-17
   Days after onset:14
Entered: 2007-02-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPH: DTAP + HIB (NO BRAND NAME) / UNKNOWN MANUFACTURER UNKNOWN / 1 UN / SC
HEP: HEP B (NO BRAND NAME) / UNKNOWN MANUFACTURER UNKNOWN / 1 UN / SC
IPV: POLIO VIRUS, INACT. (NO BRAND NAME) / UNKNOWN MANUFACTURER UNKNOWN / 1 UN / SC
PPV: PNEUMO (NO BRAND NAME) / UNKNOWN MANUFACTURER UNKNOWN / 1 UN / SC
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER UNKNOWN / 1 UN / SC

Administered by: Unknown       Purchased by: Unknown
Symptoms: Somnolence
SMQs:, Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypoglycaemia (broad)

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: NONE
Current Illness: NONE
Preexisting Conditions: NONE
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: PATIENT RECIVED THE DATP, IPV, PREVNAR, ROTATEG #1,AND HEPB AT 7 WEEKS OLD. AFTER THE VACCINA TION SHE WAS SLEEPY FOR 7 DAYS. HER APPOTITE WAS NOT CHANGED BUT I HAD TO WAKE HER UP FOR HER BOTTLE. AFTER EXACTLY 7 DAYS SHE CAME BACK TO NORMAL R0UTINE. I THINK SHE HADE A ABNORMAL REACTION THAT CALLED "MARKED INCREASE IN SLEEPING TIME"


VAERS ID: 273320 (history)  
Form: Version 1.0  
Age: 0.5  
Gender: Male  
Location: Michigan  
Vaccinated:2007-02-28
Onset:2007-02-28
   Days after vaccination:0
Submitted: 2007-03-02
   Days after onset:2
Entered: 2007-03-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (NO BRAND NAME) / UNKNOWN MANUFACTURER NOT SURE / 3 LL / IM
HIBV: HIB (NO BRAND NAME) / UNKNOWN MANUFACTURER NOT SURE / 3 RL / IM
PPV: PNEUMO (NO BRAND NAME) / UNKNOWN MANUFACTURER NOT SURE / 3 RL / IM
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER NOT SURE / 1 MO / PO

Administered by: Private       Purchased by: Private
Symptoms: Abdominal pain upper, Crying, Discomfort, Dyskinesia, Erythema, Grunting, Infrequent bowel movements, Pain, Sleep phase rhythm disturbance, Urine output decreased
SMQs:, Acute renal failure (broad), Anaphylactic reaction (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Retroperitoneal fibrosis (broad), Dyskinesia (narrow), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Depression (excl suicide and self injury) (broad), Chronic kidney disease (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: no
Preexisting Conditions: only acid reflux
Allergies:
Diagnostic Lab Data: watching baby to see if better or not...
CDC Split Type:

Write-up: Vaccine RotaTeq received oraally on 2/28/2007, baby seemed uncomfortable that night and would cry when layed back to feed...when falling asleep would twist and turn a jerk stomach as if in pain. Has not had a bowl movement since Vaccine and has limited urine in diaper. Symptoms started 2/28 evening and continued 3/1 all day. On 3/1 doctor wall called and assured us that the old vaccine caused side affects but not the new one. Baby is obviously in discomfort. Seems fine one minutes then started to get red face and grunt as if in pain...still laughing. Sleeping during day a lot but not at night all of a sudden.


VAERS ID: 274641 (history)  
Form: Version 1.0  
Age: 4.0  
Gender: Female  
Location: Texas  
Vaccinated:2007-03-21
Onset:2007-03-22
   Days after vaccination:1
Submitted: 2007-03-23
   Days after onset:1
Entered: 2007-03-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 5 UN / IM
HEPA: HEP A (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 2 UN / IM
IPV: POLIO VIRUS, INACT. (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 4 UN / IM
MMR: MEASLES + MUMPS + RUBELLA (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 2 UN / IM
RVX: ROTAVIRUS (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 3 UN / IM
VARCEL: VARICELLA (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 2 UN / IM

Administered by: Private       Purchased by: Public
Symptoms: Bacterial infection, Injection site cellulitis, Injection site erythema, Oedema peripheral, Pyrexia
SMQs:, Cardiac failure (broad), Angioedema (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

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

Write-up: Five vaccinations given on 3/21/07, 2 in left thigh, no reaction. 3 given in right thigh causing severe swelling, redness at site, and fever, cellulitis at injection site. Required antibiotics for bacterial infection.


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