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From the 10/8/2021 release of VAERS data:

Found 3,102 cases where Patient Died and Vaccination Date from '2007-08-01' to '2020-11-30'



Case Details

This is page 14 out of 311

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VAERS ID: 318749 (history)  
Form: Version 1.0  
Age: 0.2  
Sex: Male  
Location: Unknown  
Vaccinated:2008-04-04
Onset:2008-07-02
   Days after vaccination:89
Submitted: 2008-07-11
   Days after onset:9
Entered: 2008-07-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 RL / IM
HIBV: HIB (HIBERIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 LL / IM
MEN: MENINGOCOCCAL (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 1 LL / IM
PNC: PNEUMO (PREVNAR) / PFIZER/WYETH - / UNK UN / IM
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. - / UNK MO / PO

Administered by: Other       Purchased by: Other
Symptoms: Autopsy, Death, Metabolic function test, Neurological examination
SMQs:

Life Threatening? Yes
Birth Defect? No
Died? Yes
   Date died: 2008-07-02
   Days after onset: 0
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: LEVETIRACETAM; LANSOPRAZOLE
Current Illness: APNEA ; SEIZURE
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: UNK
CDC Split Type: R0000398G

Write-up: This male subject was enrolled in the prophylactic open study 110870 (MenACWY-TT-057). On 4 April 2008, he received the 1st dose of HIB-MENCY-TT (IM L thigh) and of PEDIARIX (IM R thigh). The subject received concomitantly PREVNAR (IM) and ROTATEQ vaccines (po). Medical conditions at the time of the event included apnea and seizure. Concomitant medications included PREVACID and KEPPRA. On 02 July 2008, 89 days after the 1st dose of PEDIARIX, 89 days after the 1st dose of HIB-MENCY-TT, this five-month-old subject died. The event was disabling, life-threatening, clinically significant (or requiring intervention). The subject died on 02 July 2008, cause of death is unknown. An autopsy was performed. The investigator considered that there was a reasonable possibility that the death nos may have been caused by PEDIARIX and HIB-MENCY-TT. Investigator Comments: Site was Notified of report of death on 07-03-2008, records have been requested. All data pending. 07-07-2008. After PI review, cannot completely rule out vaccine related causality, but not probable. Subject on anticonvulsants and has underwent metabolic/neurologic work-up with no significant findings. Possibility of Munchausen by Proxy, but waiting on pending results of physician and ER notes, apnea monitor results and autopsy and toxicology report. 8/22/08 Autopsy states COD as sudden unexpected infant death. Report also states Anatomical diagnosis: same as COD & aspiration of vomitus, terminal/subterminal focal bilateral. Comments: infant had complicated history of seizures, aspiration & apnea which could not be substantiated during multiple hospitalizations & ER visits & Munchausen by proxy was questioned. Autopsy showed only relatively mild terminal aspiration of vomitus. 8/5/08 Reviewed ER medical records of 7/2/2008 submitted by FDA from manufacturer. Records reveal patient well known w/history of recurrent episodes of life-threatening events of possible apnea vs seizure over the prior 2 months w/cyanosis, choking & gagging. Was on apnea/bradycardia monitor at home. Found by parent vomiting & poorly responsive. Started CPR & ACLS by EMS. Arrived in ER in full arrest & unable to resuscitate.


VAERS ID: 318889 (history)  
Form: Version 1.0  
Age: 0.5  
Sex: Male  
Location: New Jersey  
Vaccinated:2008-06-25
Onset:2008-06-26
   Days after vaccination:1
Submitted: 2008-07-14
   Days after onset:18
Entered: 2008-07-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (TRIPEDIA) / SANOFI PASTEUR U2397CA / 3 RL / UN
HIBV: HIB (ACTHIB) / SANOFI PASTEUR UF362AB / 3 LL / UN
PNC: PNEUMO (PREVNAR) / PFIZER/WYETH C65929 / 3 LL / UN

Administered by: Private       Purchased by: Other
Symptoms:
SMQs:

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2008-06-26
   Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ZANTAC, lisinopril
Current Illness: None
Preexisting Conditions: Premature at birth, status post intrauterine drug exposure, status post apnea of prematurity. PMH: Prematurity-33wks. Special needs. Birth mother abused ETOH and cocaine
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: None stated. 8/11/08 Gross autopsy findings: Visceral congestion. Diaper rash. Full report pending. 10/20/2008 Autopsy received. COD-Sudden unexplained death in infancy. Manner of death natural. Infant found unresponsive with abundant vomitus.


VAERS ID: 319501 (history)  
Form: Version 1.0  
Age: 0.3  
Sex: Female  
Location: Tennessee  
Vaccinated:2008-05-05
Onset:2008-05-22
   Days after vaccination:17
Submitted: 2008-06-06
   Days after onset:15
Entered: 2008-07-17
   Days after submission:41
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B129AA / 1 LL / IM
HIBV: HIB (ACTHIB) / SANOFI PASTEUR UF329AA / 1 RL / IM

Administered by: Public       Purchased by: Public
Symptoms: Death
SMQs:

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2008-05-22
   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: Unknown
Current Illness: None
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data:
CDC Split Type: TN08020

Write-up: Reported to office patient deceased. 9/22/08-autopsy report received-COD sudden unexpected infant death associated with inappropriate sleeping environment. Found dead while sleeping on an adult mattress on floor with pillows and blankets. Anatomical diagnosis:Thymic petechiae. Pulmonary edema. Cerebral edema. Medical intervention. Facial abrasions, mild and tongue contusion.


VAERS ID: 319533 (history)  
Form: Version 1.0  
Age: 21.0  
Sex: Female  
Location: Maryland  
Vaccinated:2008-06-03
Onset:2008-06-20
   Days after vaccination:17
Submitted: 2008-07-17
   Days after onset:27
Entered: 2008-07-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0053X / 3 LA / IM

Administered by: Unknown       Purchased by: Unknown
Symptoms: Autopsy, Death, Spleen disorder
SMQs:

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2008-06-20
   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: None
Current Illness: None
Preexisting Conditions: Reported allergy to penicillin and cephid 3/5/09-records received-Allergic to penicillin.
Allergies:
Diagnostic Lab Data: None - apparently healthy young woman 8/22/08-records received-cardiac blood neg for ethanol; urine (+) for ethanol=16 mg/dl; liver (+) for acetaldehyde (incidental finding). 3/5/09-records received-pap smear normal. 2/4/09-records received-CBC WNL, chemistry WNL. 2/12/08 ECG abnormal mild tricuspid regurgitation, 2D Doppler frequent premature ventricular contractions. 4/30/09-records received-lung specimen showed diffuse edema and intraalveolar hemorrhages. Staphylococcus aureus negative.
CDC Split Type:

Write-up: Pt received her 3rd and final dose of HPV vaccine on 6/3/08. Per mother patient was found dead, in bed on 6/22/08, in her dorm room at an out-of-state college. According to the autopsy the patient had been dead for about 48 hours. According to mother autopsy was negative except for splenic inflammation. 8/22/08 Autopsy report also states Final Diagnoses: Cardiac arrest, cause undetermined w/recent history of PAC w/otherwise normal EKG; normal echocardiogram 2/08; no evidence of myocarditis; acute pulmonary edema; slight splenomegaly; cardiac blood neg for ethanol; urine (+) for ethanol=16 mg/dl; liver (+) for acetaldehyde (incidental finding). 3/5/09-records received for DOS 8/22/07-seen for routine visit and first annual pap test..PE normal. First HPV vaccine administered. 2/4/09-records received for DOS 11/20/07-C/O chronic PAC and irregular heart beat.


VAERS ID: 319810 (history)  
Form: Version 1.0  
Age: 15.0  
Sex: Female  
Location: Illinois  
Vaccinated:2007-08-06
Onset:2007-09-20
   Days after vaccination:45
Submitted: 2008-07-18
   Days after onset:302
Entered: 2008-07-21
   Days after submission:3
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0012U / 3 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Convulsion, Death, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Systemic lupus erythematosus (broad), Arrhythmia related investigations, signs and symptoms (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? Yes
Birth Defect? No
Died? Yes
   Date died: 2007-09-20
   Days after onset: 0
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown. PMH: 1 prior seizure 8/2007. 4/28/09 Additional records received from PCP at CDC''s request. Pt in for OV 1/30/07 with c/o allergy sx and requesting HPV#1-given 0012U. Returned 3/22/07 for HPV#2-given 1427F with Boostrix AC52B012AA. Mild URI 4/25/07. OV 6/12/07 in F/U to ER visit for seizure on 6/11/07. Syncope noted. Sent for tests. OV 6/28/07 Echo and blood work reportedly WNL. Syncope again noted. PE WNL. OV 7/5/07 EEG normal. EIA? Retuned 8/6/07 for HPV#3 given 0012U. PFTs reportedly normal.
Allergies:
Diagnostic Lab Data: Unknown. Labs and Diagnostics: Tox screen (-).
CDC Split Type: WAES0807USA02139

Write-up: Information has been received from a certified medical assistant concerning a 14 year old female who was vaccinated with a first dose of GARDASIL and experienced syncope. She was taken to an emergency room and released. The patient was vaccinated with a second dose of GARDASIL (unspecified time). Subsequently, the patient experienced her first seizure (unspecified time) and was taken to the emergency room (no further details provided). The patient was vaccinated with a third dose of GARDASIL at 15 years old. Approximately 27-JUN-2008, two weeks after the third dose, the patient developed a complication. She was taken to the hospital by ambulance but passed away during the transport from an unknown cause. The physician has asked the mother for the autopsy report. The reporting medical assistant considered the syncope, seizure and "a complication" were considered to be immediately life-threatening and disabling. Additional information has been requested. 2/13/09 Autopsy report received. COD: Seizure Disorder. Summary Diagnoses: Clinical history of seizure disorder. Pulmonary congestion and edema. Passive visceral congestion. 2/20/2009 ER received from CDC. Pt presented to ER via EMS following witnessed seizure activity with fall from standing. Upon EMS arrival pt had agonal respirations and was pulseless in V-fib at 650. Upon arrival in ER unresponsive, pupils fixed and dilated, no cardiac activity. Resuscitation unsuccessful and pt expired.


VAERS ID: 320329 (history)  
Form: Version 1.0  
Age: 0.3  
Sex: Male  
Location: Texas  
Vaccinated:2008-05-14
Onset:2008-05-15
   Days after vaccination:1
Submitted: 2008-07-18
   Days after onset:64
Entered: 2008-07-24
   Days after submission:6
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B145AA / 2 RL / IM
HIBV: HIB (ACTHIB) / SANOFI PASTEUR UF330AA / 2 LA / IM
PNC: PNEUMO (PREVNAR) / PFIZER/WYETH C65043 / 2 LL / IM
RV5: ROTAVIRUS (ROTATEQ) / MERCK & CO. INC. 1888U / 2 MO / PO

Administered by: Private       Purchased by: Public
Symptoms: Autopsy, Death, Life support, Myocarditis, Respiratory arrest, Unresponsive to stimuli
SMQs:, Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (broad), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2008-05-18
   Days after onset: 3
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: None 8/1/08-records received-Congested for past several days. Cough symptoms for approximately 1 week secondary to seasonal allergies.
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data: Autopsy reports myocarditis as cause of death 8/6/08-records received-EEG:abnormal organic encephalopathy. CT brain-question of diffuse cerebral edema.
CDC Split Type:

Write-up: Pt found 5-15-08 @ 2110 by mother unresponsive, not breathing. He had been fed 4 oz and given TYLENOL for temp at 2040 hrs, then put in his crib, on abdomen with face turned to side, at 2100 she rushed him to ER at local hospital where CPR was performed and pt transferred via helicopter to another hospital. Pt on life support until 5-18-08 when it was stopped and he expired. 8/1/08-records received for DOS 5/16/08-5/18/08-presented in cardiopulmonary arrest, resuscitative efforts included CPR, intubation, mechanical ventilation. Hypothermic on presentation with rectal temperature of 91.6, hypoglycemia with blood sugar 16, metabolic acidosis. Prior to event C/O fussy all day running low grade fever, placed in crib on abdomen, found white, lump with face buried in cover. Drove child to hospital. PE: agonal respirations not compatible with life. Pupils nonreactive to light, fixed. No spontaneous movement of extremities. Deep tendon reflexes absent. 8/11/08-records received-Findings:Myocarditis. Inflammation and necrosis, myocardium. Interstitial edema, epiglottis. Tracheobronchitis, chronic. The inflammatory lesions observed in heart are consistent with either acute viral infection or post-viral syndrome.


VAERS ID: 320407 (history)  
Form: Version 1.0  
Age: 0.38  
Sex: Female  
Location: Michigan  
Vaccinated:2008-07-14
Onset:2008-07-16
   Days after vaccination:2
Submitted: 2008-07-24
   Days after onset:8
Entered: 2008-07-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS AC21B129AA / 2 LL / IM
HIBV: HIB (PEDVAXHIB) / MERCK & CO. INC. 1125F / 2 LL / IM
PNC: PNEUMO (PREVNAR) / PFIZER/WYETH 808702K / 2 RL / IM

Administered by: Unknown       Purchased by: Unknown
Symptoms: Brain injury, Coma, Convulsion, Death, Nuclear magnetic resonance imaging abnormal
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? Yes
Birth Defect? No
Died? Yes
   Date died: 2008-07-23
   Days after onset: 7
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 7 days
   Extended hospital stay? Yes
Previous Vaccinations:
Other Medications:
Current Illness: None
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data: Final MRI results: marked abnormal loss of gray-white differentiation and edema in the frontal and parietaloccipital areas 8/11/08-records received- MRI brain acute anoxic ischememic injury within the bilateral basal ganglia and bilateral occipital lobes, suggests two separate etiologies one would be diffuse hypoxia and the other posterior circulation infarcts from low/slow flow in left vertebral artery. Mild degree of brachycephaly. Marked loss of gray white differentiation with edema involving the frontal and parietoccipital regions.
CDC Split Type:

Write-up: Patient presented to the ED on 7/16/08 with seizure activity that was difficult to contol after starting to have seizures at home. She was finally stabilized then transferred to the PICU at hospital. After being here she had again started to have uncontrolled seizures. She was started on multiple seizure medications (Phenobarbital, Fosphenytoin, Pyridoxine) but still not controlled so placed into a Pentobarbital coma. This was initially weaned with a recurrence of seizures, so placed back into a Pentobarbital coma and Keppra was added. This was again weaned with the recurrence of seizures. Parents then decided that with the amount of brain damage noted on imaging that they would like to withdraw support. The patient then passed a few hours after support was withdrawn. 7/29/08-pending. no significant trauma, no gross natural disease, brain and spinal cord retained for neuropathology exam. 8/11/08-records received for DOS 7/16-7/23/08-presented to ED after seizure, had low grade fever since Monday of last week 2 days after immunizations. Intubation. Bulging pulsating fontanelle, DX:seizure activity with cerebral edema.


VAERS ID: 320423 (history)  
Form: Version 1.0  
Age: 49.0  
Sex: Female  
Location: Georgia  
Vaccinated:2007-09-24
Onset:2007-10-01
   Days after vaccination:7
Submitted: 2008-07-25
   Days after onset:298
Entered: 2008-07-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
YF: YELLOW FEVER (NO BRAND NAME) / UNKNOWN MANUFACTURER 050VFA121Z / 1 UN / SC

Administered by: Unknown       Purchased by: Unknown
Symptoms: Death
SMQs:

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2007-10-24
   Days after onset: 23
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions: 1.Systemic Lupus Erythenmatosis (vs. Rheumatoid Arthritis)2. Chronic renal Insufficiency 3.Hypertension 4. s/p Cerebrovascular Accident-2003
Allergies:
Diagnostic Lab Data: See case summary sent to VAERS
CDC Split Type:

Write-up: See deatailed case summary sent to VAERS


VAERS ID: 320713 (history)  
Form: Version 1.0  
Age: 70.0  
Sex: Female  
Location: Oregon  
Vaccinated:2008-07-21
Onset:2008-07-22
   Days after vaccination:1
Submitted: 2008-07-24
   Days after onset:2
Entered: 2008-07-29
   Days after submission:5
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. 0860U / 1 RA / IM
TTOX: TETANUS TOXOID, ADSORBED (NO BRAND NAME) / SANOFI PASTEUR U2120BA / UNK LA / IM

Administered by: Private       Purchased by: Private
Symptoms:
SMQs:

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2008-07-22
   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:
Current Illness: None
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Unknown adverse event. Patient received vaccines and passed away within 24 hrs. Autopsy scheduled 7/24/08. 10/14/08 MR and Death Cert received from PCP. Pt seen 7/21/08 with Assessment: Healthy 70 year old. PE WNL. Pt expired at unknown time 7/22/08 of unknown causes. Autopsy deferred by ME. COD: Unknown causes.


VAERS ID: 320862 (history)  
Form: Version 1.0  
Age: 50.0  
Sex: Female  
Location: Montana  
Vaccinated:2007-09-26
Onset:2007-10-26
   Days after vaccination:30
Submitted: 2008-07-30
   Days after onset:278
Entered: 2008-07-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. 6185U / UNK RA / UN
TDAP: TDAP (ADACEL) / SANOFI PASTEUR C2734AA / UNK RA / UN

Administered by: Public       Purchased by: Unknown
Symptoms: Chemotherapy, Death, Diplegia, Fall, Lung neoplasm malignant, Myelitis transverse
SMQs:, Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Malignancy related therapeutic and diagnostic procedures (narrow), Guillain-Barre syndrome (broad), Accidents and injuries (narrow), Demyelination (narrow), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Non-haematological malignant tumours (narrow), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2008-01-06
   Days after onset: 72
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 18 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: PPD
Current Illness: None
Preexisting Conditions: HX: Lung cancer 8/11/08-records received-PMH:obesity adenocarcinoma of lung.
Allergies:
Diagnostic Lab Data: Lung cancer 2 years with chemotherapy 8/11/08-records received- NCV abnormal evidence of primary muscle disorder. Glucose elevated, AST and ALT elevation of 144 and 177. MRI normal. CSF leukocytosis. Culture negative. on 1/6/08 began hypotensive with oxygen saturation 82%.
CDC Split Type:

Write-up: Brother states patient developed "Transverse myelitis" from the MMR vaccine then the patient "Fell down and died". Developed paralysis in legs one week after shot. 8/11/08-records received for DOS 12/12/07-1/6/08- DX: Paraparesis secondary to transverse myelitis. Death secondary to pulmonary embolism. Admitted for evaluation of lower extremity weakness for 2-3 weeks, with shooting pain in feet on 12/14/07-balance difficulties noted, tingling in left upper extremity prior to hospitalization Upgoing plantar reflex noted on right side, lower extremity reflex loss at ankles and left patella. Autopsy refused by family.


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