National Vaccine
Information Center

Your Health. Your Family. Your Choice.

MedAlerts Home
Search Results

Found 3,130 cases where Vaccine targets HPV (HPV2 or HPV4 or HPV9 or HPVX) and Disabled and Vaccination Date on/before '2019-05-31'

Case Details

This is page 14 out of 313

Result pages: prev   5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23   next


VAERS ID: 305693 (history)  
Form: Version 1.0  
Age: 12.0  
Sex: Female  
Location: Florida  
Vaccinated:2007-08-13
Onset:2007-09-02
   Days after vaccination:20
Submitted: 2008-02-26
   Days after onset:177
Entered: 2008-02-26
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0245U / 1 LA / UN
TD: TD ADSORBED (DITANRIX) / GLAXOSMITHKLINE BIOLOGICALS AC52B016BA / UNK LA / UN

Administered by: Private       Purchased by: Private
Symptoms: Anterior spinal artery syndrome, Laboratory test abnormal, Leukoencephalomyelitis, Monoplegia
SMQs:, Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Noninfectious encephalitis (narrow), Demyelination (narrow), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 13 days
   Extended hospital stay? Yes
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None. PMH: none. Allergic to PCN and Septra.
Allergies:
Diagnostic Lab Data: Tests confirmed acute disseminated encephalomyelitis (ADEM). Labs and Diagnostics: Spinal Arteriogram revealed no AV malformations. MR of spine c/w inflammatory process /demyelination. UC (+) for E. coli and Enterobacter. CSF WNL.
CDC Split Type:

Write-up: On September 2, 2007, patient''s left leg became paralyzed. She was taken to the emergency room and hospitalized for 13 days. The doctors at hospital diagnosed her with non-infectious A.D.E.M. 04/11/2008 MR received from hospital for DOS 9/6-10/2008 where pt was sent for diagnostic testing to r/o AVM. D/C DX: was Spinal cord anterior spinal artery infarct. Pt was transfered to another facility where Final DX was made. Pt initially had presented to local facility with sudden onset L lower extremity plegia. 04/28/2008 MR received for DOS 9/10-15/2007 with D/C DX: Acute Demyelinating Encephalomyelitis (ADEM). Urinary Tract infection. Pt admitted after transfer from above admission. Pt initially presented with Left leg weakness/paralysis and upper back pain. Upon admission pt was unable to void and later had urinary incontinence. Tx with solumedrol and abx for UTI. At D/C pt still with decreased strength of LLE, depressed reflexes and unable to bear weight independantly. Using a walker. Will continue with Outpt rehab. 1/20/2010 Patient stil has not been able to walk or run normal. She is still receiving physical therapy 2x a week. Follow-up Information 06-MAY-2008:


VAERS ID: 305823 (history)  
Form: Version 1.0  
Age: 20.0  
Sex: Female  
Location: Kentucky  
Vaccinated:2007-10-12
Onset:2007-10-26
   Days after vaccination:14
Submitted: 2008-02-26
   Days after onset:123
Entered: 2008-02-27
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 1062U / 2 LA / UN

Administered by: Private       Purchased by: Private
Symptoms: Arthralgia, Joint swelling, Parvovirus B19 serology positive
SMQs:, Haemodynamic oedema, effusions and fluid overload (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: parvovirus B19 PCR - positive
CDC Split Type: WAES0802USA04191

Write-up: Information has been received from a health professional concerning a 20 year old female with no illness at the time of vaccination and no pertinent medical history or drug reactions/allergies who on 12-OCT-2007 was vaccinated with a second dose of GARDASIL (lot# 658560/1062U) in the left arm at 9:15 AM. On 26-OCT-2007 the mother described patient had joint pain and swelling. An evaluation by a rheumatologist was performed and reported negative findings. On 12-FEB-2008 the mother reported that the patient was positive for parvovirus. At the time of reporting it was unknown if the patient had recovered from the events. Additional information is not expected. The health care professional considered arthralgia, positive for papovirus and swelling to be disabling.


VAERS ID: 306721 (history)  
Form: Version 1.0  
Age: 16.0  
Sex: Female  
Location: Florida  
Vaccinated:2007-11-17
Onset:2008-02-07
   Days after vaccination:82
Submitted: 2008-03-07
   Days after onset:29
Entered: 2008-03-10
   Days after submission:2
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 1060U / 1 UN / IM

Administered by: Other       Purchased by: Other
Symptoms: Neurological symptom
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 6 days
   Extended hospital stay? Yes
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: None 4/8/08-records received-PMH: Depression.
Allergies:
Diagnostic Lab Data: 4/8/08-records received-LP normal. MRI brain normal. CT head negative. WBC 16.31, absolute neurtrophils 13.6. M. IgG 2.06. Urine cutlure no growth.
CDC Split Type: WAES0802USA06248

Write-up: Information has been received from a physician via a company representative concerning a 17 year old who on an unspecified date was vaccinated with Gardasil IM. On approx 07-FEB-2008, "about 3 weeks ago" the patient developed neurological symptoms and was hospitalized for one week. The neurologist at the hospital diagnosed her with Miller Fisher variance of Guillain-Barre syndrome. At the time of reporting the patient "improved but she''s undergoing therapy" and has not recovered. No further information was provided. The reporter felt that Miller Fisher variance of Guillain-Barre syndrome was disabling and required hospitalization. Additional information has been requested. 4/8/08-records received for DOS 2/6-2/12/08- DC DX: Guillain-Barre variant. Developed cough and diarrhea week prior to admission. Also had vomiting and fevers. On morning of admission developed tingling in hands and feet and dysarthric speech, blurry vision and difficulty with walking. Treated with IVIG with improvement of ataxia and dysarthria. CDC''s CISA staff has reviewed this case and concluded that this case is not GBS.


VAERS ID: 307168 (history)  
Form: Version 1.0  
Age: 39.0  
Sex: Female  
Location: Unknown  
Vaccinated:2007-09-06
Onset:0000-00-00
Submitted: 2008-03-14
Entered: 2008-03-17
   Days after submission:3
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0530U / 1 UN / IM

Administered by: Other       Purchased by: Other
Symptoms: Abdominal X-ray, Biopsy bone marrow, Body temperature increased, Chills, Insomnia, Lethargy, Malaise, Pain, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Xanax; Nexium; Remeron
Current Illness: Gastrooesophageal reflux disease; Drug hypersensitivity; Allergic reaction to antibiotics
Preexisting Conditions: Depression PMH: allergies to erythromycin, biaxin & demerol. LGSIL 7/05. Interstitial cystitis.
Allergies:
Diagnostic Lab Data: Abdominal computed; X-ray; Echocardiography; Bone marrow biopsy; Body temperature $g100 deg LABS: pap smear 9/5 neg. LABS: CBC, CRP, ANA & chemistry WNL. Blood c/s neg. RA (-). Hep B surface AB (+). TSH 6.42 (H). Urine c/s (+) for enterococcus. Burgdorferi (-). Cancer antigen 125 16.9 (H). Echocardiogram WNL. EGD revealed colon polyps, biopsies of stomach, duodenum & esophagus done & revealed only mild reflux esophagitis. Abdomen/pelvis CT scan, CXR & pelvic US WNL.
CDC Split Type: WAES0803USA01222

Write-up: Information has been received from a physician, concerning herself, a 40 year old female with gastrooesophageal reflux disease, drug hypersensitivity to meperidine (DEMEROL), erythromycin and clarithromycin (BIAXIN), and a history of depression, who on 05-SEP-2007 was vaccinated IM with the first dose of Gardasil (lot # not reported). Concomitant therapy included esomeprazole magnesium (NEXIUM), mirtazapine (REMERON) and alprazolam (XANAX). In approximately September 2007 ("following the vaccination"), the physician felt lethargic and couldn''t sleep. On 06-NOV-2007 she was vaccinated IM with the second dose of Gardasil (lot #655154/1210U). Following the second dose, she developed fevers greater than 100 degrees F, which have continued for 4 months, along with body pain and rigors. She had diagnostic labs and testing performed, including a computed axial tomography (CAT) scan of the chest and abdomen, x-ray, echocardiogram and bone marrow biopsy (dates and results not provided). The physician stated she hadn''t been able to work for 3 months, due to her significant malaise. She reported seeing another physician (details not provided). At the time of this report, the physician had not recovered from the events. The physician indicated that the events were serious as disabling. Additional information has been requested. 4/11/08 Received OB/GYN medical records of 8/23/07 & labs of 9/5/07. 4/15/08 Received primary GYN record of 11/6/07 where received HPV #2, 1210U left deltoid. Reported no side effects from HPV #1. 5/30/08 Reviewed PCP medical records from 7/2007-3/2008 which reveal patient experienced depression & under psych care. Unable to work. In 11/2007, had fever x 5 days, abdominal cramping & increased stools. Tx w/meds & improved until fever returned 12/2007 W/HA & severe fatigue. Meds adjusted & felt better by 1/2008. Fever recurred 2-3/2008 PCP felt could be related to psych meds. Meds adjusted. ID & GYN consult done. No dx stated. Felt better & was able to return to work 4/2008.


VAERS ID: 307686 (history)  
Form: Version 1.0  
Age: 14.0  
Sex: Female  
Location: New York  
Vaccinated:2008-01-26
Onset:2008-02-01
   Days after vaccination:6
Submitted: 2008-03-14
   Days after onset:41
Entered: 2008-03-17
   Days after submission:3
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 3 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Blister, Mouth ulceration, No reaction on previous exposure to drug, Pyrexia
SMQs:, Severe cutaneous adverse reactions (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
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
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: WAES0802USA03079

Write-up: Information has been received from a consumer concerning her 17 year old daughter who on 11-JUL-2007, 20-SEP-2007, 26-JAN-2008 was vaccinated with her first, second and third dose of Gardasil, respectively. It was reported that the patient did not have a reaction to the first or second dose. Within two weeks after her third dose she experienced a high fever and blisters down her throat. It was reported that she missed work and school due to the reaction. The consumer''s sister also had a similar reaction to Gardasil (WAES#0710USA03615). Additional information has been requested. follow up 2/12/2010- follow up information received from the physician regarding a 14 year old caucasian female patient (previously reported as 17 years old) with no previous medical history or no illness at the time of vaccination, who on 11-jul-2007. at 10:04 am was vaccinated IM in the left arm with the first dose of HPV 6 11 16 18 vaccine (yeast) (lot# 658100/05250) and on 20-sep-2007 at 6: 46 pm, was vaccinated IM in the left arm with the second dose of HPV 11 16 18 vlp vaccine (yeast) lot# 657736/0389u. on 31-jul-2007, the patient experienced a fever began 2 weeks following the 1st vaccination. also experienced oral ulcers. fever persisted x 1 week. again developed fever and mouth sores 2 weeks following dose 2. no reactions after the third vaccination. the patient recovered 1-2 weeks after onset of symptoms.


VAERS ID: 307342 (history)  
Form: Version 1.0  
Age: 18.0  
Sex: Female  
Location: South Carolina  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2008-03-18
Entered: 2008-03-19
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 1 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Abdominal pain, Disturbance in attention, Dysmenorrhoea, Fatigue, Headache, Hypomenorrhoea, Impaired driving ability, Injection site pain, Menstruation irregular, Pain, Respiratory tract congestion, Streptococcus identification test negative, Viral infection
SMQs:, Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Noninfectious encephalopathy/delirium (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Depression (excl suicide and self injury) (broad), Fertility disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: Pollen allergy
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: throat culture - strep throat test negative
CDC Split Type: WAES0803USA01272

Write-up: Information has been received from a pharmacy technician concerning her 18 year old daughter with no medical history and an allergy to pollen, who in April 2007, was vaccinated with a first dose of Gardasil. There was no concomitant medication. The patient reported that the dose was painful. Subsequently, the patient had difficulty driving home. In June 2007 the patient was vaccinated with a second dose of Gardasil. The patient reported that the dose was painful. Subsequently, the patient had difficulty driving home. On 27-DEC-2007 the patient was vaccinated with a third dose of Gardasil. The patient reported that the dose was painful. The patient''s mother went with her daughter for the third dose. The patient began her menses on 30-DEC-2007 (she had it 2 weeks prior) in which there was a lot of pain prior to and during the menses. The patient was also very tired. The menses lasted five days. It was reported that after the New Year the patient returned to college and felt very congested. The patient went to see a physician near college who told the patient that she probably had a virus. The patient began to feel worse and was seen by the physician a second time. The physician treated her with azithromycin (ZITHROMAX). The time between the two doctor visits was unspecified. Two weeks later on 13-JAN-2008 the daughter began her menses and experienced a lot of stabbing pain of the lower abdomen prior to and during menses. The patient was also very tired. The menses lasted five days. On 20-FEB-2008 the patient began her menses with pain prior to and during the menses. The patient was also very tired. The menses lasted three days and was very light. On 06-MAR-2008 the patient experienced pain in the abdomen (a sign her menses could be starting again). It was reported that the patient was experiencing headaches during her periods, which have been more frequent then before. In order to treat the headaches the patient was taking ibuprofen (MOTRIN). The patient''s mother spoke to the physician on 25-FEB-2008. A throat culture was performed for strep throat and was negative. At the time of the report, the patient had not recovered. No product quality complaint was involved. The pain during injection, stabbing pain in the lower abdomen, painful menses, tiredness, headaches, light menses, difficulty driving, congestion, frequent menses, and probable virus were considered to be disabling due to the patient not being able to "concentrate" and not being able to "keep up with her school work." Additional information has been requested.


VAERS ID: 307343 (history)  
Form: Version 1.0  
Age: 17.0  
Sex: Female  
Location: Unknown  
Vaccinated:2008-03-04
Onset:2008-03-05
   Days after vaccination:1
Submitted: 2008-03-18
   Days after onset:12
Entered: 2008-03-19
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 1448U / 3 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Back pain, Hallucination, Headache, Hyperaesthesia, Nausea, Pyrexia, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Dementia (broad), Psychosis and psychotic disorders (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: ADDERALL TABLETS
Current Illness: Attention deficit disorder; drug hypersensitivity
Preexisting Conditions: No reaction on previous exposure to vaccine. PMH: Broken nose. Allergic to cough/cold meds.
Allergies:
Diagnostic Lab Data: Unknown. Labs and Diagnostics: CT Abd & pelvis-no acute findings. CXR WNL. Chem WNL. LFTs WNL except Alk Phos 71. CBC WNL. UA WNL except trace ketones. Blood and UC (-). Labs and diagnostics: CBCs with normal WBCs but high monos(17) and eosinophils (9). Chemistry WNL. Alk phos (51)and CK (32) low. Blood cx (-). UC (-). CRP 3.81. Lyme (-). VZV IgG (+). VZV IgM (-). LP WNL. Head CT (-). Labs and Diagnostics: Vit D 25OH 22.2. Vit B12 1475. Antigliadin IgG 60.98. PFTs WNL. Lyme IgG/IgM (+). Lyme C6 peptide (+).
CDC Split Type: WAES0803USA01494

Write-up: Information has been received from a registered nurse concerning her 17 year old daughter with attention deficit disorder and an allergy to over-the-counter cold preparations, who on 04-MAR-2008 at 16:30 was vaccinated with a third dose of Gardasil. Concomitant therapy included ADDERALL TABLETS. On 05-MAR-2008, eight hours post vaccination the patient experienced a high fever, hallucinations, severe back pain, severe headache, skin sensitivity, nausea and vomiting and was hospitalized. It was reported that the patient tolerated the first and second doses of Gardasil well. At the time of the report, the patient had not recovered. No product quality complaint was involved. The high fever, hallucinations, severe back pain, severe headache, skin sensitivity, nausea and vomiting were considered to be disabling. Additional information has been requested. 4/10/2008 MR received for ER visit 3/5/2008 with DX: Primary DX: R Flank Pain. Additional DX: Fever-unknown origin. Pt presented to ER from MD''s office with fever, chills, sudden onset R sided flank pain, nausea and vomiting. Pt reports fatigue and weakness as well. PE (+) for tenderness at the R CVA, fever, and pain. D/C home in improved condition. 5/13/2008 MR received for DOS 3/6-8/2008 with no clear D/C DX. Rheumatology Impression is: Back pain that is probably of a systemic problem. ID consult Impression: Fever and infection of the back, r/o sacroilitis, r/o vertebral osteomyelitis, r/o non-infectious etiology. Pt presented unable to walk 2'' to back pain. Pain is localized to SI joint area. 5/06/2008 MR received for ER visit 3/10/2008 with DX: Headache. Pt presented following D/C from inpt stay with worsening h/a assoc with neck and back pain. 07/21/2008 MR received from Allergy/Immunology consult dated 3/12/2008 to 6/20/2008 with DX: Gardasil induced vasculitis. On the evening of the 3rd Gardasil vax pt awoke with fever, feeling delusional with aching chills. Pt continued to have fevers, excrutiating headaches and back pain which worsened following LP. PE (+) for glassy eyes, dehydration, unable to stand, diffuse weakness. Pulse increased from 50 to 90 upon standing. Started on Prednisone with 80-90% improvement. Seen again 6/20/08 with improvment of sx of vasculitis. Reports post-exercise exhaustion.


VAERS ID: 307394 (history)  
Form: Version 1.0  
Age: 13.0  
Sex: Female  
Location: California  
Vaccinated:2007-03-01
Onset:2007-05-25
   Days after vaccination:85
Submitted: 2008-03-19
   Days after onset:299
Entered: 2008-03-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0187U / 3 - / -

Administered by: Unknown       Purchased by: Unknown
Symptoms: Abdominal pain, Amyotrophic lateral sclerosis, Electromyogram abnormal, Lumbar puncture, Muscular weakness, Nerve conduction studies abnormal, Neuropathy, Nuclear magnetic resonance imaging, Paralysis flaccid, Respiratory failure, Sleep study abnormal, Swelling, Urinary incontinence, Vomiting
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (narrow), Acute pancreatitis (broad), Angioedema (broad), Peripheral neuropathy (narrow), Retroperitoneal fibrosis (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Hypersensitivity (broad), Respiratory failure (narrow), Hypokalaemia (broad)

Life Threatening? Yes
Birth Defect? No
Died? Yes
   Date died: 2009-03-15
   Days after onset: 660
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 24 days
   Extended hospital stay? Yes
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none 4/8/08-recor ds received-PMH: attention deficit hyperactivity disorder and congenital strabismus. Migraines. Cognitive delay, developmental delay and motor delay. Allergies:strawberries cause an itch. In May sustained injury with pain in leg which improved but never returned completely to normal. 4/16/08-records received-PMH: Pityriasis lichennoides. Allergy to strawberries causes itching. Attention deficit disorder.
Allergies:
Diagnostic Lab Data: EMG and nerve conduction studies suggest motor neuronopathy vs neuropathy 4/8/09-records received- EEG normal. MRI brain showed slightly prominent cerebellar fissures but otherwise normal. MRI spine normal. West Nile, hepatitis B were negative. Urine organic acids elevated lactic acid. T4 and TSH normal. Heavy metal screen normal. Acylcarnitine profile normal. CSF protein elevated 54, lymphocytes 86 and monocytoid cells 14. CSF amino acids showed nonspecific variations from normal of serine, alanine, citrulline, valine, methionine, beta aminoisobutyric acid, lysine and histidine. triglycerides 429. December 2007 EMG and nerve conduction studies with dignosis of multifocal motor neuropathy. MRI at that time showed nerve root enhancement. 4/16/08-records received-EEG normal. MRI brain and spine normal. Elevated lactic acid level in urine. Sleep study mild obstructive sleep apnea syndrome with one episode of hypoxemia without hypoventilation worse in REM sleep and supine. MRI of lumbar spine mild enhancement of lumbar nerve roots however this was done after a lumbar puncture and findings may be secondary to lumbar puncture. 4/16/08-CPK increased of 313 and slightly elevated anticardiolipin IgM of 20.3. EEG normal. MRI brain and spine normal. Elevated lactic acid level in urine. LP: mildly elevated protein of 46 with normal glucose. MRI of lumbar spine mild enhancement of lumbar nerve roots however this was done after a lumbar puncture and findings may be secondary to lumbar puncture.
CDC Split Type:

Write-up: Progressive muscle weakness resulting in flaccid paresis of all 4 extremities, respiratory insufficiency. 4/8/08-records received for DOS 2/4-2/17/08-DC DX: autoimmune motor neuropathy, provisional. Possible motor neuron disease. Admission 3/14-3/25/08-DC DX: Muscular weakness. Seizures. Received IVIG, treated with plasmapheresis. Admitted with C/O progressive muscular weakness over the 3 weeks prior to admission increased immunomodulation. Seizure after completion of solumedrol. Remained post ictal for several hours. No diagnosis made during this admission. Genetic evaluation for mitrochondrial disease sent to include evaluation for Pompe disease. In May sustained injury with pain in leg which improved but never returned completely to normal. Developed worsening limping and loss of strength in distal left lower extremity. Between August and October of 2007 developed symptoms in right arm. Received IVIG at that time and again January 2008 with improvement in right handed tremor but worsening function status especially in ambulation, stair climbing and standing from seated position. Feb 4-17 2008 hospitalized received plasmapheresis with improved ability to stand for short periods. C/O headaches and nausea. She may have chronic inflammatory demyelinating myopathy versus a multifocal motor neuropathy. After discharge to follow up with specialist in ALS. 4/16/08-records received-for DOS 1/2-1/3/08-DC DX: Multifocal neuropathy versus chronic demyelinating polyneuropathy. LP: mildly elevated protein of 46 with normal glucose. Unable to perform activities of daily living. IVIG treatment. PE: left lower and right upper extremity weakness and atrophy with some mild weakness of right lower extremity. 4/16/08-clinical consult case review template received: CPK increased of 313 and slightly elevated anticardiolipin IgM of 20.3. DX: chronic inflammatory demyelinating polyneuropathy. 1/2/08-urinary incontinence may have been due to her reduced ability to mobilize given her leg weakness. Plasmapheresis. 3/14/08-admitted for progressively worsening weakness and increased immunomodulation. During treatment with IV Solu-Medrol, one seizure and was post-ictal for several hours. Shortness of breath with vital capacity of 48%. Restrictive and obstructive component to her lung involvement. 4/5/08-DX: primary muscular atrophy the syndrome of progressive lower motor neuron loss. Third seizure during sleep study. Currently on a trial of Cytoxan. Impression: ten month history of progressive muscular weakness with lower motor neuron signs and status post multiple different trials of immunosuppressant medications. 4/16/08-records received-for DOS 1/2-1/3/08-DC DX: Multifocal neuropathy versus chronic demyelinating polyneuropathy.Unable to perform activities of daily living. IVIG treatment. PE: left lower and right upper extremity weakness and atrophy with some mild weakness of right lower extremity. 6/17/09 Autopsy report received from CDC - DOS 3/17/09 Clinical Diagnosis: Atypical progressive lower motor neuron disease, ventilator dependence, gastrostomy tube, hypercalcemia, seizures. I. Extensive demyelination, involving the lateral and anterior columns of the cervical, thoracic and lumbar spinal cord, with macrophage and lymphocytic infiltration. Severe loss of motor neurons, cervical, thoracic, and lumbar spinal cord. Rare neurons with amorphous cytoplasmic inclusions, frontal cortex, substantia nigra, locus ceruleus, medulla oblongata, and spinal cord. Neurogenic atropy, skeletal muscle. II. Acute brochopneumonia, lungs. III. Mild steatosis, liver. IV. Gastrostomy tube, stomach, in proper position. Follow-up: Paralysis - involving 4 extremities trunk and possibly the diaphragm given that her FVC = 27%. She also has significant persistent nausea / vomiting, intermittent abdominal pain, and extremity swelling. Her condition continues to deteriorate and now she is on BIPAP.


VAERS ID: 307627 (history)  
Form: Version 1.0  
Age: 16.0  
Sex: Female  
Location: Delaware  
Vaccinated:2008-02-05
Onset:2008-03-03
   Days after vaccination:27
Submitted: 2008-03-19
   Days after onset:15
Entered: 2008-03-21
   Days after submission:2
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Abdominal pain upper, Activities of daily living impaired, Epstein-Barr virus antibody negative, Fatigue, Hyperhidrosis, Splenomegaly, Ultrasound abdomen abnormal
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Retroperitoneal fibrosis (broad), Dementia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: ultrasound slightly enlarged spleen; serum Epstein-Barr negative
CDC Split Type: WAES0803USA02393

Write-up: Information has been received from a physician concerning a 16 year old female who on 05-FEB-2008 was vaccinated with Gardasil (lot number not provided). On 03-MAR-2008 the patient experienced extreme fatigue, severe stomach pains and breaking out in sweat. The patient also stated "the pain is so extreme, she can not go to school." The patient''s extreme fatigue and severe stomach pains and breaking out in sweat persisted. On an unspecified date, the patient had a mononucleosis test performed-result was negative. On an unspecified date an ultrasound was also performed, results indicated that the patients spleen was slightly enlarged. Extreme fatigue, severe stomach pains and breaking out in sweat were considered to be disabling. Additional information has been requested.


VAERS ID: 308330 (history)  
Form: Version 1.0  
Age: 17.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2008-01-26
Onset:2008-02-02
   Days after vaccination:7
Submitted: 2008-03-26
   Days after onset:52
Entered: 2008-03-27
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 1448U / 2 UN / IM

Administered by: Other       Purchased by: Other
Symptoms: Full blood count normal, Laboratory test normal, Muscular weakness, Nuclear magnetic resonance imaging normal, Paraesthesia, Thyroid function test normal
SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data: magnetic resonance 02?/??/08 - head and spine normal; complete blood cell 02?/??/08 - normal; blood chemistry 02?/??/08 - normal; thyroid function test 02?/??/08 - normal 6/3/08-records received-MRI thoracic spine, mild degenerative disc changes. MRI lumbar spine normal and cervical lordosis. EEG normal.
CDC Split Type: WAES0803USA03845

Write-up: Information has been received from a physician, concerning a white female student (age not reported), with no pertinent medical history, who on 23-NOV-2007 was vaccinated with the first dose, and on 26-JAN-2008 was vaccinated, IM, with the second dose of GARDASIL (lot #659653/1448U). The physician noted that on 06-NOV-2007, the patient had been vaccinated with a dose of HAVRIX and a dose of MENACTRA. There was no illness at the time of vaccination. On 02-FEB-2008 the patient experienced paresthesias of both feet and up her legs, with some weakness, that continued through the month. On 26-FEB-2008 she experienced "pins and needles" of her arms and shoulders. The patient visited the physician, and on an unknown date, diagnostic testing included a magnetic resonance imaging (MRI) of the head and spine, a complete blood count (CBC), blood chemistries and a thyroid panel, all with normal results. At the time of this report, the outcome of the events was not recovered. The physician considered the events to be serious as disabling or incapacitating. Additional information has been requested. 6/3/08-records received-seen on 2/6/08 with C/O chronic back pain (pine and needles) both legs, hip and ankle. Trouble sleeping. Began on Monday. Feels unbalanced when standing. Urinary incontinence. PE Babinski decreased on right. Unable to stand on tiptoes. Romberg wobbly. Reflexes normal. Sensation in left toe dull. 4/30/08 symptoms continue but improving now intermittent. Neurologist: post viral syndrome. Flu vaccine administered in November along with Gardasil. Meningitis vaccine in November.


Result pages: prev   5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23   next

New Search

Link To This Search Result:

https://www.medalerts.org/vaersdb/findfield.php?EVENTS=ON&PAGENO=14&VAX[]=HPV2&VAX[]=HPV4&VAX[]=HPV9&VAX[]=HPVX&VAXTYPES[]=HPV&DISABLE=Yes&VAX_YEAR_HIGH=2019&VAX_MONTH_HIGH=05


Copyright © 2020 National Vaccine Information Center. All rights reserved.
21525 Ridgetop Circle, Suite 100, Sterling, VA 20166