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Found 6884 cases where Vaccine is HPV4 and Serious

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VAERS ID: 290294 (history)  
Form: Version 1.0  
Age: 15.0  
Sex: Female  
Location: Georgia  
Vaccinated:2007-09-05
Onset:2007-09-05
   Days after vaccination:0
Submitted: 2007-09-10
   Days after onset:5
Entered: 2007-09-11
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0181U / 1 LA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U2394BA / 1 RA / IM

Administered by: Private       Purchased by: Private
Symptoms: Chest pain, Dizziness, Dyspnoea, Headache, Nausea, Oxygen supplementation, Pyrexia
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Respiratory failure (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: None
Preexisting Conditions: None - NKDA or food allergy. PMH: symptoms of depression and anxiety with SI on and off.
Allergies:
Diagnostic Lab Data: Hospital admission. Given SoluMedrol and Benadryl IV in office. O2 2L/nic. labs and Diagnostics: CXR WNL.
CDC Split Type:

Write-up: Chest pain, shortness of breath, headache, dizziness, nausea, fever. 09/12/2007 MR received for DOS 9/6-7/2007 for admitting DX of allergic reaction MCV, dyspepsia, tachycardia. Consult reports possible allergic reaction to meningococcal vaccine. Diagnostic Impression: MDD. Pt with agoraphobia. Possible reaction to MCV. Generalized anxiety.


VAERS ID: 290331 (history)  
Form: Version 1.0  
Age: 23.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2007-08-07
Onset:2007-08-14
   Days after vaccination:7
Submitted: 2007-09-05
   Days after onset:22
Entered: 2007-09-12
   Days after submission:7
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0525U / 2 RA / IM

Administered by: Private       Purchased by: Unknown
Symptoms: Blood creatine phosphokinase increased, Lymphadenopathy, Myalgia, Red blood cell sedimentation rate normal, Trismus
SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Myocardial infarction (broad), Dystonia (narrow), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

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: Developed lymph swelling in neck~HPV (Gardasil)~1~23.00~In Patient
Other Medications: Allegra, Zoloft, Flonase, Albuterol, BCP
Current Illness: None known
Preexisting Conditions: Celexa= nightmares PMH: mono, allergic rhinitis, asthma, hx of suppressed immune system. TMJ tx w/night guard.
Allergies:
Diagnostic Lab Data: Sed rate = nl; CPK - was 471 (8/21) - 179 (8/30/07) LABS: WBC 8.2, lymphs # (H) 3.2. CT scan of neck revealed slightly enlarged bilateral lymph nodes. CPK 500. Monospot & strep screen neg.
CDC Split Type:

Write-up: This was pt''s second Gardasil vaccine on 8/7/07. She developed symptoms 8/14 and was seen at hospital 8/20, 8/21, 8/22/07. She was suffering from myalgias, trismus, "lockjaw" and slight neck adenopathy. Her neck CT was normal. 9/18/07 Received hospital medical records which reveal patient experienced severe neck pain & swelling w/inability to open her mouth. After 1st vax 6/07 had tenderness in right clavicle & neck area. Saw pcp & dx w/reaction to vax. Resolved over approx 1-2 mos. Received 2nd vax in 8/07. Approx 1 week later developed severe pain in right neck & axilla w/enlarged lymph nodes. States pain was so severe that she could not open her mouth. Saw pcp who again dx w/reaction to vax but referred to ER due to severity. Exam revealed full ROM of neck w/tenderness & palpable tender lymph nodes of neck & right axillary. D/C to home. No improvement & returned to ER on 9/21. Tx w/IVF, pain med & IV steroids. Improved in ER & d/c to home. Returned to ER on 8/22 for repeat labs & recheck of symptoms. CPK improved but continued w/same symptoms but no adenopathy noted on exam. Right arm exam WNL but w/increased tone to bicep/tricep area w/good ROM, strength & sensation. Tx w/pain med & benzodiazapam w/excellent relief. D/C to home & f/u w/pcp. Final ER DX: 8/20/07 reactive lymphadenopathy, probable viral illness, ? TMJ syndrome, questionable AE to vaccine. Final ER DX: 8/21/07 myalgias w/extremely low grade rhabdomyolysis & ? serum immune complex type hypersensitivity reaction to vaccine. Final ER DX: 8/22/07 myalgias w/low grade rhabdomyalisis.


VAERS ID: 290576 (history)  
Form: Version 1.0  
Age:   
Sex: Female  
Location: Massachusetts  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2007-09-13
Entered: 2007-09-14
   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: Dizziness, Hypotension, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad)

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:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: WAES0709USA00586

Write-up: Information has been received from a physician concerning a female who was vaccinated with a 0.5 ml first dose of Gardasil (date not reported). There was no concomitant medication. Subsequently, the patient "experienced dizziness and fainted" after receiving Gardasil. While in the physician''s office it was reported that the patient also experienced "hypotensiveness". The office called 911. The patient went to the hospital and was released after four hours. Subsequently, the patient recovered. The reporting physician considered dizziness, hypotensiveness and fainting to be immediately life-threatening events. Additional information has been requested.


VAERS ID: 290580 (history)  
Form: Version 1.0  
Age: 15.0  
Sex: Female  
Location: Unknown  
Vaccinated:2007-05-16
Onset:2007-08-23
   Days after vaccination:99
Submitted: 2007-09-13
   Days after onset:21
Entered: 2007-09-14
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEPA: HEP A (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK UN / UN
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0388U / 1 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Asthenia, Fatigue, Mental status changes
SMQs:, Dementia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (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, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: WAES0709USA00835

Write-up: Information has been received from a nurse concerning a 15 year old female who on 16-MAY-2007 was vaccinated with a first dose of Gardasil (lot 657622/0388U). On 16-MAY-2007, the patient was concomitantly vaccinated with hepatitis A vaccine (inactive) (manufacturer unknown). The nurse reported that the patient stated that she received a second dose of Gardasil, but the nurse noted that there was no documentation that the patient received a second dose of Gardasil. On 23-AUG-2007 the patient experienced fatigue, altered mental status and weakness. On 25-AUG-2007, the patient was brought to the emergency room. The patient was hospitalized (details and length of hospitalization not provided). The patient was visited by her physician on 25-AUG-2007, 26-AUG-2007, and 28-AUG-2007. At the time of this report, the outcome was unknown. Additional information has been requested.


VAERS ID: 290659 (history)  
Form: Version 1.0  
Age: 25.0  
Sex: Female  
Location: Tennessee  
Vaccinated:2007-04-16
Onset:2007-04-16
   Days after vaccination:0
Submitted: 2007-09-14
   Days after onset:151
Entered: 2007-09-17
   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: Drug exposure during pregnancy, Drug screen positive, Laboratory test, Smear cervix, Substance abuse, Ultrasound scan
SMQs:, Drug abuse and dependence (narrow), Depression (excl suicide and self injury) (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (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, ? days
   Extended hospital stay? Yes
Previous Vaccinations:
Other Medications: vitamins (unspecified)
Current Illness:
Preexisting Conditions: Substance abuse
Allergies:
Diagnostic Lab Data: ultrasound; urine drug screen - positive; Pap test - Results not reported; laboratory test - Unspecified, Results not reported
CDC Split Type: WAES0709USA00784

Write-up: Information has been received from a registered nurse concerning a 25 year old female with a history of drug abuse who on 07-AUG-2006 was vaccinated intramuscularly with a 0.5 ml first dose of Gardasil (Lot #653937/0637F). On 11-OCT-2006 the patient was vaccinated with a second dose of Gardasil. On 16-APR-2007 the patient was vaccinated with a third dose of Gardasil. Concomitant therapy included prenatal vitamins (unspecified). Subsequently the patient became pregnant. The patient''s last menstrual period was on 11-JUN-2007 and the estimated date of delivery was 17-MAR-2008. On unspecified dates a urine drug screen, ultrasound, pap test, and a prenatal screen was performed. The patient contacted the physician by telephone. On 09-JUL-2007 the patient was hospitalized for substance abuse. At the time of the report the patient''s outcome was unknown. Additional information has been requested.


VAERS ID: 290711 (history)  
Form: Version 1.0  
Age: 12.0  
Sex: Female  
Location: Oklahoma  
Vaccinated:2007-08-08
Onset:2007-08-20
   Days after vaccination:12
Submitted: 2007-09-17
   Days after onset:28
Entered: 2007-09-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0469U / 1 RA / UN
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U2391BA / 1 RA / UN
TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS AC52B0186A / 6 LA / UN

Administered by: Unknown       Purchased by: Unknown
Symptoms: Abasia, Agitation, Anxiety, Dizziness, Echocardiogram normal, Electrocardiogram abnormal, Electroencephalogram normal, Loss of consciousness, Paraesthesia, Syncope, Tremor
SMQs:, Torsade de pointes/QT prolongation (broad), Peripheral neuropathy (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (narrow), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Dystonia (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (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, 3 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Melatonin 2mg
Current Illness: N/A
Preexisting Conditions: ADHD. PMH: ADD. Anxiety.
Allergies:
Diagnostic Lab Data: EKG-showed possible borderline QT syndrome, EEG-normal, Echocardiagram-normal. Labs and Diagnsotics: EKG with prolonged QT. Echo WNL. CT head w/ no abnormalities. EEG normal
CDC Split Type:

Write-up: Patient fainted at cheerleading practice and was transported to ER. Patient continued to lose consciousness, shake, become extremely agitated and could not walk. She complained of prickly feelings in legs. Patient was admitted to hospital for further tests for 3 days. Patient gained back use of legs during the last two days in the hospital. Patient still is having dizziness and is seeking further treatment. 10/15/2007 MR received for DOS 8/21-23/2007 with D/C DX: Syncope. Conversion Disorder. Child had syncopal episode preceded by dizziness and lightheadedness. Was passed out for 15 minutes. (+) anxiety. Had several syncopal episodes in the ER. PE was WNL. Per 60 day follow: The patient has been advised to not get the 2 remaining GARDASIL vaccinations. Possible medication induced long QT.


VAERS ID: 290871 (history)  
Form: Version 1.0  
Age: 16.0  
Sex: Female  
Location: Unknown  
Vaccinated:2007-08-12
Onset:2007-08-12
   Days after vaccination:0
Submitted: 2007-09-18
   Days after onset:37
Entered: 2007-09-19
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 1 UN / IM

Administered by: Other       Purchased by: Other
Symptoms: Pharyngeal oedema, Respiratory tract congestion, Swollen tongue, Upper respiratory tract congestion
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Oropharyngeal allergic conditions (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Pulmicort, Xopenex, Loratadine, Nasonex
Current Illness: Pollen allergy; House dust allergy; Mycotic allergy
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: WAES0709USA02075

Write-up: Information has been received from a health professional concerning a 16 year old female with pollen allergy, house dust allergy and mycotic allergy who on approximately 12-AUG-2007 was vaccinated with the first dose of Gardasil. Concomitant therapy included mometasone furoate (NASONEX), budesonide (PULMICORT), loratadine and levalbuterol hydrochloride (XOPENEX). On approximately 12-AUG-2007 the patient experienced throat swelling, tongue swelling and became congested following vaccination. On 13-AUG-2007, the patient sought medical attention during an office visit. The patient was treated with diphenhydramine HCl (BENADRYL) and an unspecified inhaler. Subsequently, the patient recovered from throat swelling, tongue swelling and became congested. The reporting nurse considered the patient''s throat swelling, tongue swelling, and congestion to be immediately life-threatening. Additional information has been requested.


VAERS ID: 292025 (history)  
Form: Version 1.0  
Age: 20.0  
Sex: Female  
Location: California  
Vaccinated:0000-00-00
Onset:2007-07-27
Submitted: 2007-09-17
   Days after onset:52
Entered: 2007-09-20
   Days after submission:3
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 3 UN / UN

Administered by: Private       Purchased by: Other
Symptoms: Asthenia, Injection site pain, Musculoskeletal stiffness, Myositis, Tendonitis
SMQs:, Rhabdomyolysis/myopathy (broad), Dystonia (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Arthritis (broad), Tendinopathies and ligament disorders (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? Yes
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: WAES0708USA01882

Write-up: Information has been received from a physician concerning a female patient in her 20''s who was vaccinated with a first and second dose of Gardasil. The physician reported that the patient had unusual soreness at the injection site after the first and second injection. He also reported that the patient had unusual stiffness and weakness with local mechanical trouble after she was given the third dose of Gardasil. The patient had not recovered as of this report day. The physician reported that this is one of the three patient who experienced similar experiences. Additional information has been requested. This is in follow-up to report (s) previously submitted on 9/17/2007. Initial and follow up information has been received from a physician concerning a 20 year old female student who was vaccinated with a first and second dose of GARDASIL vaccine. In follow up it was reported that on 27-JUL-2007, the patient had shoulder tendinitis and myositis. On 01-SEP-2007 patient recovered. The reporter indicated that the patient''s adverse event left shoulder tendinitis and myositis was disabling. The physician reported that this is one of the three patient who expereinced similar experiences. Additional information is not expected.


VAERS ID: 292999 (history)  
Form: Version 1.0  
Age: 22.0  
Sex: Female  
Location: California  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2007-09-17
Entered: 2007-09-20
   Days after submission:3
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 3 UN / UN

Administered by: Private       Purchased by: Other
Symptoms: Asthenia, Injection site pain, Musculoskeletal stiffness, Vaccine positive rechallenge
SMQs:, Dystonia (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Arthritis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? Yes
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: WAES0709USA00883

Write-up: Information has been received from a physician concerning a female patient in her 20''s who was vaccinated with a first and second dose of Gardasil. The physician reported that the patient had unusual soreness at the injection site after the first and second injection. He also reported that the patient had unusual stiffness and weakness with local mechanical trouble after she was given the third dose of Gardasil. The patient had not recovered as of this report day. The physician reported that this is one of the three patient who experienced similar experience. Additional information is not expected.


VAERS ID: 293000 (history)  
Form: Version 1.0  
Age: 27.0  
Sex: Female  
Location: California  
Vaccinated:0000-00-00
Onset:2007-07-27
Submitted: 2007-10-01
   Days after onset:66
Entered: 2007-09-20
   Days after submission:11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 1 UN / UN

Administered by: Private       Purchased by: Other
Symptoms: Asthenia, Injection site pain, Musculoskeletal stiffness, Myositis, Tendonitis, Vaccine positive rechallenge
SMQs:, Rhabdomyolysis/myopathy (broad), Dystonia (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Arthritis (broad), Tendinopathies and ligament disorders (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? Yes
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: WAES0709USA00884

Write-up: Information has been received from a physician concerning a female patient in her 20''s who was vaccinated with a first and second dose of Gardasil. The physician reported that the patient had unusual soreness at the injection site after the first and second injection. He also reported that the patient had unusual stiffness and weakness with local mechanical trouble after she was given the third dose of Gardasil. The patient had not recovered as of this report day. The physician reported that this is one of the three patients who experienced similar experiences. Additional information has been requested. This is in follow-up to report (s) previously submitted on 09/17/2007. Initial and follow up information has been received from a physician concerning a 27 year old female who was vaccinated with a first and second dose of GARDASIL. The physician reported that the patient had unusual soreness at the injection site after the first and second injection. He also reported that the patient had unusual stiffness nad weakness with local mechanical trouble after she was given the third dose of GARDASIL. In follow up it was reported that on 27-JUL-2007, patient had shoulder tendenitis and myositis). On 01-SEP-2007 patient recovered. The reporter indicated that the patient''s adverse event left shoulder tendenitis and myositis were disabling. The physician reported that this is one of three patient who experienced similar experiences. Additional information is not expected.


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