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From the 4/23/2021 release of VAERS data:

Found 20,989 cases where Vaccine targets Tetanus (6VAX-F or DT or DTAP or DTAPH or DTAPHEPBIP or DTAPIPV or DTAPIPVHIB or DTIPV or DTP or DTPHEP or DTPHIB or DTPIHI or DTPIPV or DTPPHIB or TD or TDAP or TDAPIPV or TTOX) and Serious and Vaccination Date on/after '2000-01-01'



Case Details

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VAERS ID: 151748 (history)  
Form: Version 1.0  
Age: 0.25  
Sex: Male  
Location: Pennsylvania  
Vaccinated:2000-03-22
Onset:2000-04-17
   Days after vaccination:26
Submitted: 2000-04-20
   Days after onset:3
Entered: 2000-05-09
   Days after submission:19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (INFANRIX) / SMITHKLINE BEECHAM 918A2 / 1 LL / IM
HBHEPB: HIB + HEP B (COMVAX) / MERCK & CO. INC. 14775 / 1 RL / IM
IPV: POLIO VIRUS, INACT. (NO BRAND NAME) / PASTEUR MERIEUX INST. P09052 / 1 LA / SC

Administered by: Private       Purchased by: Public
Symptoms: Sudden infant death syndrome
SMQs:, Neonatal disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2000-04-17
   Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: hydrocortisone for dermatitis 3/22/2000
Current Illness: NONE
Preexisting Conditions: Possible milk protein allergy, dermatitis.
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: SIDS death within one months of IZ. Autopsy being performed.


VAERS ID: 151749 (history)  
Form: Version 1.0  
Age: 0.25  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2000-04-04
Onset:2000-04-13
   Days after vaccination:9
Submitted: 2000-04-19
   Days after onset:6
Entered: 2000-05-09
   Days after submission:20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (ACEL-IMUNE) / PFIZER/WYETH 466024 / 1 RL / IM
HBHEPB: HIB + HEP B (COMVAX) / MERCK & CO. INC. 1192J / 1 LL / IM
IPV: POLIO VIRUS, INACT. (NO BRAND NAME) / PASTEUR MERIEUX INST. P1232 / 1 - / SC

Administered by: Private       Purchased by: Public
Symptoms: Sudden infant death syndrome
SMQs:, Neonatal disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2000-04-14
   Days after onset: 1
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NONE
Current Illness: NONE
Preexisting Conditions: Feeding problems first 3 days of life only.
Allergies:
Diagnostic Lab Data: NONE
CDC Split Type:

Write-up: SIDS 10 days post vax.


VAERS ID: 151758 (history)  
Form: Version 1.0  
Age: 1.4  
Sex: Female  
Location: New Hampshire  
Vaccinated:2000-01-26
Onset:2000-02-03
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2000-05-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (INFANRIX) / SMITHKLINE BEECHAM 920A2 / 4 LA / IM
HIBV: HIB (ACTHIB) / CONNAUGHT LABORATORIES 61044AB / 4 RA / IM
IPV: POLIO VIRUS, INACT. (POLIOVAX) / CONNAUGHT LTD. R02362 / 3 LA / -
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. 1082J / 1 RA / SC

Administered by: Private       Purchased by: Other
Symptoms: Drooling, Immune system disorder, Myasthenic syndrome, Pneumonia aspiration, Respiratory arrest
SMQs:, Anaphylactic reaction (broad), Malignancy related conditions (narrow), Dyskinesia (broad), Dystonia (broad), Parkinson-like events (broad), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Hypersensitivity (broad), Respiratory failure (narrow), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 23 days
   Extended hospital stay? Yes
Previous Vaccinations:
Other Medications:
Current Illness: NONE
Preexisting Conditions: NONE
Allergies:
Diagnostic Lab Data: Antibody titer levels, CT scan, MRI, EMG, CBC, spinal tap, EKG, esophageal scope.
CDC Split Type:

Write-up: Received shots on 01/26 (Wednesday). Sunday 30th - slight drooling. 01/31 hospitalized for aspiration pneumonia due to thick mucus. Thursday 02/03 respiratory arrest. In ICU and hospital for the month of February. Various tests were conducted. Dx of autoimmune myasthenia gravis. A follow up report received 8/2/2000 adds: Call to nurse indicates thyrectomy not done, pt is weaned off all meds now and is in remission. Case complete.


VAERS ID: 151760 (history)  
Form: Version 1.0  
Age: 0.2  
Sex: Male  
Location: West Virginia  
Vaccinated:2000-05-03
Onset:2000-05-03
   Days after vaccination:0
Submitted: 2000-05-04
   Days after onset:1
Entered: 2000-05-09
   Days after submission:5
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (TRIPEDIA) / CONNAUGHT LABORATORIES U0045CA / UNK LL / IM
HIBV: HIB (HIBTITER) / PFIZER/WYETH 591313A / UNK RL / IM
IPV: POLIO VIRUS, INACT. (POLIOVAX) / CONNAUGHT LTD. R01012 / UNK RL / SC

Administered by: Private       Purchased by: Public
Symptoms: Crying, Pallor, Vasodilation procedure
SMQs:, Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Depression (excl suicide and self injury) (broad), Hypotonic-hyporesponsive episode (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, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: NONE
Preexisting Conditions: NONE
Allergies:
Diagnostic Lab Data: Vital signs - stable.
CDC Split Type:

Write-up: Immediately, post vax, developed vasoactive phenomenom with blanching and mottle and shrill, persistent uncontrolable crying. Vital signs were stable.


VAERS ID: 151761 (history)  
Form: Version 1.0  
Age: 17.0  
Sex: Female  
Location: Georgia  
Vaccinated:2000-05-04
Onset:2000-05-04
   Days after vaccination:0
Submitted: 2000-05-08
   Days after onset:4
Entered: 2000-05-09
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. 0044J / 1 RA / SC
TD: TD ADSORBED (NO BRAND NAME) / CONNAUGHT LABORATORIES U0114BA / 6 LA / IM

Administered by: Private       Purchased by: Private
Symptoms: Cellulitis, Diarrhoea, Hypersensitivity, Injection site mass, Myalgia, Oedema peripheral, Pain, Pyrexia, Vomiting, White blood cell count increased
SMQs:, Rhabdomyolysis/myopathy (broad), Cardiac failure (broad), Acute pancreatitis (broad), Angioedema (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (narrow), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (narrow)

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? Yes, 4 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: PPD (Connaught C0018AA)
Current Illness:
Preexisting Conditions: carpal tunnel syndrome, GER, headaches
Allergies:
Diagnostic Lab Data: WBC elevated to 23. CBC, Blood C&S.
CDC Split Type:

Write-up: On 5/5/00, right arm started swelling, pt had myalgia, fever, and chills. On 5/6/00, pt developed high fever, large red firm area on right arm, chills, and vomiting. Pt was admitted to hospital and given Ancef and IV fluids for right arm cellulitis. Follow-up reports that the child is still having problems with swollen arm, soreness, diarrhea (due to massive doses of antibotics). The diagnosis is a severe allergic reaction and cellulitis.


VAERS ID: 151801 (history)  
Form: Version 1.0  
Age: 22.0  
Sex: Female  
Location: Florida  
Vaccinated:2000-04-29
Onset:2000-04-29
   Days after vaccination:0
Submitted: 2000-05-04
   Days after onset:5
Entered: 2000-05-10
   Days after submission:6
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEPA: HEP A (HAVRIX) / SMITHKLINE BEECHAM 639A4 / 1 - / IM
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. 133J / 2 - / SC
TD: TD ADSORBED (NO BRAND NAME) / CONNAUGHT LABORATORIES U0003BA / 2 - / IM

Administered by: Military       Purchased by: Military
Symptoms: Dyspnoea, Pallor, Urticaria
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (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? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: NONE
Current Illness: NONE
Preexisting Conditions: Latex, Benadryl
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Urticaria, dyspnea, pallor, approximately 15 minutes, post vax. Treated with epinephrine, IM, and Atarax, albuterol and Solu-Medrol in ER all in right deltoid. Follow-up with allergist is recommended.


VAERS ID: 151835 (history)  
Form: Version 1.0  
Age: 0.2  
Sex: Female  
Location: California  
Vaccinated:2000-04-21
Onset:2000-04-21
   Days after vaccination:0
Submitted: 2000-05-10
   Days after onset:19
Entered: 2000-05-11
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (ACEL-IMUNE) / PFIZER/WYETH 469396 / 1 RL / IM
HBHEPB: HIB + HEP B (COMVAX) / MERCK & CO. INC. - / UNK LL / IM
IPV: POLIO VIRUS, INACT. (POLIOVAX) / CONNAUGHT LTD. R0442 / 1 LL / IM

Administered by: Private       Purchased by: Other
Symptoms: Anaphylactic reaction, Grunting, Pallor
SMQs:, Anaphylactic reaction (narrow), Anaphylactic/anaphylactoid shock conditions (narrow), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow)

Life Threatening? Yes
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: UNK
Allergies:
Diagnostic Lab Data: UNK
CDC Split Type: HQ4612226APR2000

Write-up: A physician reported that a 2 month old infant, five hours post vax, became pale and developed grunting. The infant was taken to an ER and treated with oxygen, IV fluids and Solu-Medrol. The infant recovered. These events are considered medically important. Additional information, received from the physician on 4/25/2000, indicated that the 2 month old female developed an anaphylactic reaction. She remained recovered.


VAERS ID: 151837 (history)  
Form: Version 1.0  
Age: 0.36  
Sex: Female  
Location: Indiana  
Vaccinated:2000-02-25
Onset:2000-02-25
   Days after vaccination:0
Submitted: 2000-04-20
   Days after onset:54
Entered: 2000-05-11
   Days after submission:21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (INFANRIX) / SMITHKLINE BEECHAM 916A2 / 2 LL / IM
HBHEPB: HIB + HEP B (COMVAX) / MERCK & CO. INC. 1786J / 2 RL / IM
IPV: POLIO VIRUS, INACT. (POLIOVAX) / SANOFI PASTEUR PO735 / 2 LL / IM

Administered by: Public       Purchased by: Public
Symptoms: Convulsion
SMQs:, Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? Yes
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: MRI, 2 EEG''s, blood work, UA
CDC Split Type: IN200016

Write-up: Focal seizures in the mouth area starting around 12 hours after shots, lasting 3 days. Under medication now. Possibly due to vaccines. Presently on phenobarbidtol. Follow up on 11/21/2003: "Vaccine recipient did recover from the adverse events that were reported for this vaccination."


VAERS ID: 151839 (history)  
Form: Version 1.0  
Age: 1.4  
Sex: Female  
Location: New Jersey  
Vaccinated:2000-04-20
Onset:2000-04-20
   Days after vaccination:0
Submitted: 2000-04-22
   Days after onset:2
Entered: 2000-05-11
   Days after submission:19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (TRIPEDIA) / CONNAUGHT LABORATORIES U0137BA / 4 - / IM
HIBV: HIB (ACTHIB) / CONNAUGHT LABORATORIES P1290AB / 4 - / IM
IPV: POLIO VIRUS, INACT. (NO BRAND NAME) / PASTEUR MERIEUX INST. P09052 / 3 - / -

Administered by: Other       Purchased by: Public
Symptoms: Convulsion, Pyrexia, Sepsis
SMQs:, Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Sepsis (narrow), Opportunistic infections (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, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Conjunctivitis
Preexisting Conditions: Mild development delay
Allergies:
Diagnostic Lab Data: All tests-nml
CDC Split Type: NJ200012

Write-up: Pt was seen for well visit with conjunctivitis. 45 minutes post vax, pt experienced Tonic/clonic generalized seizure. Pt was seen in ER with a fever of 104.8, nml exam. Pt was admitted to rule out sepsis, antibiotics were given. Discharged on 4/22/00 with neg cultures, no fever and normal exam.


VAERS ID: 151860 (history)  
Form: Version 1.0  
Age: 49.0  
Sex: Male  
Location: Iowa  
Vaccinated:2000-04-13
Onset:2000-04-14
   Days after vaccination:1
Submitted: 2000-05-02
   Days after onset:18
Entered: 2000-05-12
   Days after submission:10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
TTOX: TETANUS TOXOID, ADSORBED (NO BRAND NAME) / PFIZER/WYETH 4988112 / UNK LA / IM

Administered by: Private       Purchased by: Public
Symptoms: Blood urea increased, Cellulitis, Depression, Diarrhoea, Erythema, Fatigue, Influenza like illness, Injection site erythema, Injection site induration, Injection site pain, Injection site swelling, Injury, Insomnia, Oral intake reduced, Palpitations, Pollakiuria, Red blood cell sedimentation rate increased, Tremor, Type III immune complex mediated reaction, Urinary hesitation, Weight decreased, White blood cell count decreased
SMQs:, Acute renal failure (broad), Anaphylactic reaction (broad), Haematopoietic leukopenia (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Arrhythmia related investigations, signs and symptoms (broad), Retroperitoneal fibrosis (broad), Pseudomembranous colitis (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Accidents and injuries (narrow), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hostility/aggression (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Depression (excl suicide and self injury) (narrow), Chronic kidney disease (broad), Hypersensitivity (narrow), Noninfectious diarrhoea (narrow), Tumour lysis syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (narrow)

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? Yes, 3 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Celexa; Aciphex; Tylenol; Vioxx; Hydrocodone w/acetaminophen
Current Illness: Left thumb crushing injury
Preexisting Conditions: depression, GERD, injury to left thumb, hyperlipidemia, nausea
Allergies:
Diagnostic Lab Data: CBC-low WBC, ultrasound of arm 5/1/00-extensive induration of left upper arm-no abscess-(bone infection) inflammation extends to periosteum. F/U: blood urea nitrogen-31mg/dl (H); ESR-28mm/hr (H);
CDC Split Type:

Write-up: Swelling, pain, redness, induration involving the entire left upper arm; associated with flu-like symptoms. Prolonged course-poorly responsive to antihistimines or antibiotics. Admitted to hospital 4/30/00. Follow-up reports that the pt still has a hard knot on the arm in the area of vax and also complained of fatigue. Per F/U; the pt was seen by the physician on 4/13/00 because of a left thumb crushing injury. He was administered Tetanus Toxoid. He was dx''d on 4/19/00 with cellulitis and administered IM ceftriaxone sodium for 2 days, then prescribed oral amoxicillin/clavulanate for 7 days. He later received IM ceftriaxone sodium for the next 3 days. The next day, the physician performed a needle aspiration to decompress the area because it was firm approx. the size of a 50 cent piece. His physician prescribed cefazolin for 3 days to be given at an infusion facility. The pt was depressed. At the infusion facility, the pt indicated that he had lost 7 pounds, had no appetite and experienced diarrhea for the past 2 weeks. On 4/30/00, his arm infection worsened; he developed streaking. He was admitted to the hospital for IV antibiotics with a dx of "Type III hypersensitivity", "arthur" reaction, "serum sickness", left arm pain and possible abscess, cellulitis and lymphangitis. He was treated also with rocecoxib. Then Citalopram was prescribed. Methylprednisolone sodium succinate was prescribed and the pt was discharged from the hospital with an additional prescrition for rabeprasole. He was prescribed propoxyphene napaylate for pain on 5/5/00. On 5/10/00, the MD noted that the pt experienced a red face, palpitations, hand shaking and urinary hesitancy with dribbling. Nitrofurantoin was prescribed and his dosage of prednisone was decreased. This did not help. Tamsulosin hydrochloride was prescribed on 5/17/00. The pt continued to have urinary frequency, hesitancy, difficulty urinating, tremors and sleeplessness. On exam, the fibrous thickened area at the injection site on his left arm had improved. Flomax was discontinued; prednisone tapering was initiated. As of 5/16/01, the pt had recovered.


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