Found 18 events with Vaccine is 'ROT'

This is page 1 out of 2

VAERS ID 264479   Vaccination Date: 2006-07-11 Age 0.2   Onset Date: 2006-07-20   Days later: 9 Sex F   Submitted: 2006-10-10 State    Entered: 2006-10-13	Life Threatening Illness? No Died? No Disability? No Recovered? Yes ER or Doctor Visit? No Hospitalized? No Current Illness: Diagnostic Lab Data: Previous Vaccinations: Other Medications: Lansoprazole 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.
Vaccination Manufacturer Lot Dose Route Site DTAPHE GLAXOSMITHKLINE   0 IM UN HIBV AVENTIS PASTEUR, INC.   0 IM UN PNC LEDERLE LABORATORIES   0 IM UN ROT UNKNOWN MANUFACTURER   0 PO
Administered by: UNK     Purchased by: UNK Symptoms: Pyrexia 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 n
VAERS ID 265207   Vaccination Date: 2006-10-23 Age 0.2   Onset Date: 2006-10-23   Days later: 0 Sex F   Submitted: 2006-10-23 State MI   Entered: 2006-10-23	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? Yes Hospitalized? No Current Illness: Diagnostic Lab Data: Previous Vaccinations: Other Medications: Preexisting Conditions:
Vaccination Manufacturer Lot Dose Route Site DTAP AVENTIS PASTEUR, INC. c2489aa 0 IM LL HIBV AVENTIS PASTEUR, INC. uf026aa 0 IM LL IPV AVENTIS PASTEUR, INC. z0240 0 IM RL PNC LEDERLE LABORATORIES b08646b 0 IM RL ROT UNKNOWN MANUFACTURER 0848f   PO
Administered by: UNK     Purchased by: UNK Symptoms: Crying Erythema Oral intake reduced Swelling Large amount of redness and edema lt leg crying non stop refusal to nurse.
VAERS ID 265890   Vaccination Date: 2006-11-01 Age 0.2   Onset Date: 2006-11-01   Days later: 0 Sex M   Submitted: 2006-11-02 State OH   Entered: 2006-11-02	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? No Hospitalized? No Current Illness: None Diagnostic Lab Data: CBC negative, Cath U/A negative. CSF negative. Cultures pending as of 11-02-2006 12:45PM Previous Vaccinations: Other Medications: none Preexisting Conditions: None
Vaccination Manufacturer Lot Dose Route Site DTAP AVENTIS PASTEUR, INC. U1965BA 0 IM LL HBHEPB MERCK & CO. INC. 0012F 0 IM RL IPV AVENTIS PASTEUR, INC. Y1032 0 IM LL PNC LEDERLE LABORATORIES B08683C 0 IM RL ROT UNKNOWN MANUFACTURER 01457 0 PO
Administered by: UNK     Purchased by: UNK Symptoms: Body temperature increased Condition aggravated Pallor 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)
VAERS ID 267380   Vaccination Date: 2006-11-15 Age 0.0   Onset Date: 2006-11-15   Days later: 0 Sex U   Submitted: 2006-11-20 State    Entered: 2006-11-20	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? Yes Hospitalized? No Current Illness: I was not ill before having the Rototech sneezed inot my eyes, but became so within seconds afterwards. Diagnostic Lab Data: Previous Vaccinations: Other Medications: Preexisting Conditions: I do not have any allergies, other than an allergic reaction to CT scan dye once.
Vaccination Manufacturer Lot Dose Route Site ROT UNKNOWN MANUFACTURER 0979F   PO
Administered by: UNK     Purchased by: UNK Symptoms: Cough Dysphonia Malaise Medication error Pain Paraesthesia At 3:30 pm, I (a registered nurse) was administering the Rototech vaccine to an infant. After delivering half of it slowly, I paused and the baby sneezed, thereby spraying much of it into both of my eyes, with slightly more into the right eye. I immediately rinsed my eyes in the sink, but started having a tingling sensation, which progressed within a minute or two into a ground glass like pain. Then I began to cough uncontrollably, which lasted for hours, until I lost my voice altogether.MY epes became very
VAERS ID 269418   Vaccination Date: 2006-11-28 Age 0.1   Onset Date: 2006-12-05   Days later: 7 Sex F   Submitted: 2006-12-19 State MI   Entered: 2006-12-19	Life Threatening Illness? No Died? No Disability? No Recovered? Yes ER or Doctor Visit? Yes Hospitalized? No Current Illness: No Diagnostic Lab Data: Previous Vaccinations: Other Medications: Preexisting Conditions:
Vaccination Manufacturer Lot Dose Route Site ROT UNKNOWN MANUFACTURER xxxxx   PO
Administered by: UNK     Purchased by: UNK Symptoms: Haematochezia 7days after rotavirus, had bloody, mucousy stools.
VAERS ID 271452   Vaccination Date: 2006-07-11 Age 0.2   Onset Date: 2006-07-20   Days later: 9 Sex F   Submitted: 2007-01-29 State    Entered: 2007-01-29	Life Threatening Illness? No Died? No Disability? No Recovered? Yes ER or Doctor Visit? No Hospitalized? No Current Illness: GASTROINTESTINAL REFLUX DISEASE Diagnostic Lab Data: Body temperature 102.0 F Previous Vaccinations: Other Medications: PREVACID Preexisting Conditions: The subject had a history of gastrointestinal reflux disease which started on 29 June 2006 and continued at the time of reporting. From 29 June 2006 to 30 June 2006, she was treated with lansoprazole.
Vaccination Manufacturer Lot Dose Route Site DTAPHE GLAXOSMITHKLINE ACZIB071BA   IM LL HIBV AVENTIS PASTEUR UE864AA   IM RL PNC LEDERLE LABORATORIES AZ5969K   IM LL ROT UNKNOWN MANUFACTURER AROTA033A   PO
Administered by: OTH     Purchased by: OTH Symptoms: Blood culture negative Body temperature increased Culture urine negative Lumbar puncture Pyrexia Viral infection This female was enrolled in a prophylactic open study. On 11 July 2006, she received the 1st dose of rotavirus vaccine (HRV, po) (lot # AROTA033A), Pediarix, IM X thigh (lot # ACZIB071BA), ActHIB, IM X thigh (lot # UE864AA) and Prevnar, IM X thigh (lot # AZ5969K). The subject had a history of gastrointestinal reflux disease which started on 29 June 2006 and continued at the time of reporting. From 29 June 2006 to 30 June 2006, she was treated with Lansoprazole. On 20 July 2006, nine days after the 1st dose
VAERS ID 271922   Vaccination Date: 2007-01-26 Age 0.2   Onset Date: 2007-02-04   Days later: 9 Sex F   Submitted: 2007-02-07 State MO   Entered: 2007-02-07	Life Threatening Illness? No Died? No Disability? No Recovered? Yes ER or Doctor Visit? Yes Hospitalized? No Current Illness: None Diagnostic Lab Data: Blood in stool seen by physician Previous Vaccinations: Other Medications: none Preexisting Conditions: None
Vaccination Manufacturer Lot Dose Route Site HEP UNKNOWN MANUFACTURER unknown 0 IM UN IPV UNKNOWN MANUFACTURER unknown 0 IM UN PNC LEDERLE LABORATORIES unknown 0 ID UN ROT UNKNOWN MANUFACTURER unknown 0 PO
Administered by: PVT     Purchased by: UNK Symptoms: Haematochezia Blood in stool 8 days after first Rotavaccine
VAERS ID 272141   Vaccination Date: 2007-01-18 Age 0.3   Onset Date: 2007-01-25   Days later: 7 Sex M   Submitted: 2007-02-12 State NH   Entered: 2007-02-12	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? No Hospitalized? No Current Illness: None known Diagnostic Lab Data: Previous Vaccinations: None known~~NULL~~In Patient|None known~~NULL~~In Sibling1 Other Medications: None known Preexisting Conditions: Mild hydrocephalus
Vaccination Manufacturer Lot Dose Route Site DTAPHE GLAXOSMITHKLINE AC21B084BA 1 IM LL HIBV GLAXOSMITHKLINE UF025AA 1 IM LL PNC LEDERLE LABORATORIES B08691B 1 IM RL ROT UNKNOWN MANUFACTURER 0577F 1 PO
Administered by: UNK     Purchased by: UNK Symptoms: Sudden infant death syndrome Sudden infant death syndrome Child found dead in crib 7 days after receiving vaccines. Parents report no symptom prior to death.
VAERS ID 272461   Vaccination Date: 2007-02-02 Age 7.0   Onset Date: 2007-02-03   Days later: 1 Sex F   Submitted: 2007-02-17 State CA   Entered: 2007-02-17	Life Threatening Illness? No Died? No Disability? No Recovered? Yes ER or Doctor Visit? No Hospitalized? No Current Illness: NONE Diagnostic Lab Data: Previous Vaccinations: Other Medications: NONE Preexisting Conditions: NONE
Vaccination Manufacturer Lot Dose Route Site DTAPH UNKNOWN MANUFACTURER UNKNOWN 0 SC UN HEP UNKNOWN MANUFACTURER UNKNOWN 0 SC UN IPV UNKNOWN MANUFACTURER UNKNOWN 0 SC UN PPV UNKNOWN MANUFACTURER UNKNOWN 0 SC UN ROT UNKNOWN MANUFACTURER UNKNOWN 0 SC UN
Administered by: PVT     Purchased by: UNK Symptoms: Somnolence EMILY 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 273016   Vaccination Date: 2007-02-02 Age 0.2   Onset Date: 2007-02-16   Days later: 14 Sex U   Submitted: 2007-02-26 State CA   Entered: 2007-02-26	Life Threatening Illness? No Died? No Disability? No Recovered? Yes ER or Doctor Visit? No Hospitalized? No Current Illness: NONE Diagnostic Lab Data: none Previous Vaccinations: Other Medications: NONE Preexisting Conditions: NONE
Vaccination Manufacturer Lot Dose Route Site DTAPHE GLAXOSMITHKLINE AC21B089AA 1 IM LL HIBV MERCK & CO. INC. 1084F 1 IM LL PNC LEDERLE LABORATORIES 808670C 1 IM RL ROT UNKNOWN MANUFACTURER 0942F 1 SC UN
Administered by: UNK     Purchased by: UNK Symptoms: Diarrhoea 2wks after Rotavirus pt presented to clinic for diarrhea total of 5d. I called pt today to see how she is doing and per mom pt is fine and diarrhea has resolved.

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VAERS ID 270217   Vaccination Date: 2006-12-14 Age 0.2   Onset Date: 2006-12-14   Days later: 0 Sex M   Submitted: 2007-01-08 State CA   Entered: 2007-01-09	Life Threatening Illness? No Died? No Disability? No Recovered? Yes ER or Doctor Visit? No Hospitalized? No Current Illness: NONE Diagnostic Lab Data: NONE Previous Vaccinations: Other Medications: NONE Preexisting Conditions: NONE
Vaccination Manufacturer Lot Dose Route Site ROT UNKNOWN MANUFACTURER
Administered by: PUB     Purchased by: PUB Symptoms: Choking Cyanosis Depressed level of consciousness Respiratory rate decreased 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   Vaccination Date: 2007-01-18 Age 0.2   Onset Date: 2007-01-20   Days later: 2 Sex F   Submitted: 2007-01-22 State PA   Entered: 2007-01-22	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? No Hospitalized? No Current Illness: no Diagnostic Lab Data: Previous Vaccinations: Other Medications: zantac Preexisting Conditions: gastroesophageal reflux, fussy baby
Vaccination Manufacturer Lot Dose Route Site HIBV MERCK & CO. INC. 1015F 0 IM LL ROT UNKNOWN MANUFACTURER merck 1111F   PO
Administered by: PVT     Purchased by: PVT Symptoms: Dermatitis diaper Diarrhoea severe diarrhea and diaper rash 2 days following administration of the vaccine
VAERS ID 270977   Vaccination Date: 2007-01-16 Age 0.2   Onset Date: 2007-01-16   Days later: 0 Sex F   Submitted: 2007-01-23 State VA   Entered: 2007-01-23	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? No Hospitalized? No Current Illness: None Diagnostic Lab Data: CBC, chest w-ray, RSV, chem panel Echo:VSD, PFO Blood Cultures negative. RSV negative Abd X-ray-nonspecific gas pattern without free air seen. CXR:negative AP and lateral chest. Previous Vaccinations: Other Medications: None Preexisting Conditions: None
Vaccination Manufacturer Lot Dose Route Site DTAPHE GLAXOSMITHKLINE AC01B073AA 0 IM LL HIBV AVENTIS PASTEUR UE952AA 0 IM RL PNC LEDERLE LABORATORIES B08671B 0 IM RL ROT UNKNOWN MANUFACTURER 0319F 0 PO
Administered by: UNK     Purchased by: UNK Symptoms: Abdominal X-ray Anorexia Blood culture negative Cardiac murmur Chest X-ray Chest X-ray normal Choking Crying Echocardiogram Full blood count Gastrooesophageal reflux disease Immunisation reaction Laboratory test Oedema peripheral Respiratory arrest Screaming Skin discolouration Swelling Ventricular septal defect Virus serology test 3 hrs after immunization, child began screaming, difficult to console, refused to eat, choking, vomited, stopped breathing (10 sec), leg purple, swollen. No fever. Taken to ER: treated for reflux, heart murmur, had ECHO done, given Zantac, admitted for observation 01/24/07-records received and reviewed for DOS 01/16-01/18/07 DC DX:GE reflux Presented with unusual crying since vaccines, per parents both legs turned purple and were swollen for a period of a few hours. Child began to choke and stopped breat
VAERS ID 273140   Vaccination Date: 2007-01-08 Age 0.5   Onset Date: 2007-02-24   Days later: 47 Sex M   Submitted: 2007-02-27 State UT   Entered: 2007-02-27	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? Yes Hospitalized? No Current Illness: NONE Diagnostic Lab Data: X RAY Previous Vaccinations: Other Medications: ZANTAC Preexisting Conditions:
Vaccination Manufacturer Lot Dose Route Site DTAP AVENTIS PASTEUR C2521AA 2 IM LL FLU AVENTIS PASTEUR U2220BB 0 IM LL HEP MERCK & CO. INC. 0412F 2 IM RL IPV AVENTIS PASTEUR Y1031 2 IM LL PNC LEDERLE LABORATORIES B58845D 2 IM RL ROT UNKNOWN MANUFACTURER 1111F 1 PO
Administered by: UNK     Purchased by: UNK Symptoms: Abdominal distension Bowel sounds abnormal Dehydration Diarrhoea Gastroenteritis Intussusception Intussusception Vomiting X-ray INTUSSUSCEPTION
VAERS ID 273320   Vaccination Date: 2007-02-28 Age 0.5   Onset Date: 2007-02-28   Days later: 0 Sex M   Submitted: 2007-03-02 State MI   Entered: 2007-03-02	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? No Hospitalized? No Current Illness: no Diagnostic Lab Data: watching baby to see if better or not... Previous Vaccinations: Other Medications: Preexisting Conditions: only acid reflux
Vaccination Manufacturer Lot Dose Route Site DTAP UNKNOWN MANUFACTURER not sure 2 IM LL HIBV UNKNOWN MANUFACTURER not sure 2 IM RL PPV UNKNOWN MANUFACTURER not sure 2 IM RL ROT UNKNOWN MANUFACTURER not sure 0 PO
Administered by: PVT     Purchased by: PVT Symptoms: Abdominal pain upper Crying Discomfort Dyskinesia Erythema Grunting Infrequent bowel movements Pain Sleep phase rhythm disturbance Urine output decreased 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 fa
VAERS ID 274641   Vaccination Date: 2007-03-21 Age 4.0   Onset Date: 2007-03-22   Days later: 1 Sex F   Submitted: 2007-03-23 State TX   Entered: 2007-03-23	Life Threatening Illness? No Died? No Disability? No Recovered? Yes ER or Doctor Visit? Yes Hospitalized? No Current Illness: Diagnostic Lab Data: Previous Vaccinations: Other Medications: Preexisting Conditions:
Vaccination Manufacturer Lot Dose Route Site DTAP UNKNOWN MANUFACTURER   4 IM UN HEPA UNKNOWN MANUFACTURER   1 IM UN IPV UNKNOWN MANUFACTURER   3 IM UN MMR UNKNOWN MANUFACTURER   1 IM UN ROT UNKNOWN MANUFACTURER   2 IM UN VARCEL UNKNOWN MANUFACTURER   1 IM UN
Administered by: PVT     Purchased by: PUB Symptoms: Bacterial infection Injection site cellulitis Injection site erythema Oedema peripheral Pyrexia 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.
VAERS ID 274757   Vaccination Date: 0000-00-00 Age    Onset Date: 0000-00-00   Days later: Sex U   Submitted: 2007-03-23 State    Entered: 2007-03-26	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? Yes Hospitalized? No Current Illness: Diagnostic Lab Data: Previous Vaccinations: Other Medications: (therapy unspecified) Preexisting Conditions: UNK
Vaccination Manufacturer Lot Dose Route Site ROT UNKNOWN MANUFACTURER     PO
Administered by: OTH     Purchased by: OTH Symptoms: Hospitalisation Surgery Information has been received from a registered nurse concerning an infant who was vaccinated orally with Rotateq (Lot not provided). Concomitant therapy included other vaccines concomitantly. Subsequently, the patient had unspecified intestinal surgery and was hospitalized. The reporter felt that intestinal surgery was not related to therapy with Rotateq. It was unspecified how long the infant was in the hospital. The outcome of the intestinal surgery was not provided. Additional has been requested.
VAERS ID 275008   Vaccination Date: 0000-00-00 Age 0.2   Onset Date: 0000-00-00   Days later: Sex F   Submitted: 2007-03-27 State TX   Entered: 2007-03-27	Life Threatening Illness? No Died? No Disability? No Recovered? Yes ER or Doctor Visit? Yes Hospitalized? No Current Illness: None Diagnostic Lab Data: None Previous Vaccinations: Other Medications: None Preexisting Conditions: None
Vaccination Manufacturer Lot Dose Route Site DTAPHE GLAXOSMITHKLINE AC21B097AB 0 IM RL HIBV AVENTIS PASTEUR UE953AA 0 IM LL PNC LEDERLE LABORATORIES B36258F 0 IM LL ROT UNKNOWN MANUFACTURER 0285F 0 PO
Administered by: PUB     Purchased by: PUB Symptoms: Crying Injection site erythema Received 2month vaccines on 3/26/2007 @ 1:30pm. Site where HIB was given got reddened 4 hours later and child was crying inconsolably. Was seen by pediatrician at 5:30pm on 3/26/2007 and was given Benadryl liquid. Was followed up today and Local reaction resolved. I was notified by MD's nurse as to what transpired.Made telephone call to mother who states child now fine.