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Found 44930 cases where Vaccine is HPV4

Case Details

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VAERS ID: 326092 (history)  
Form: Version 1.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2008-08-14
Entered: 2008-08-18
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / UNK UN / IM

Administered by: Other       Purchased by: Other
Symptoms: Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (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? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: WAES0807USA03015

Write-up: Information has been received from a physician assistant concerning a female patient who on an unspecified date, was vaccinated with a dose of GARDASIL vaccine (yeast), 0.5ml, intramuscularly for HPV prevention. The physician assistant reported that the patient fainted after receiving the vaccine. The patient recovered on the same day of the vaccination. The patient sought unspecified medical attention. Additional information has been requested. /


VAERS ID: 326093 (history)  
Form: Version 1.0  
Age: 14.0  
Sex: Female  
Location: Tennessee  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2008-08-14
Entered: 2008-08-18
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 1 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Muscle spasms, Vaccine positive rechallenge
SMQs:, Dystonia (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? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: WAES0807USA03033

Write-up: Information has been received from a nurse concerning a 14 year old female patient who was vaccinated with the entire series of GARDASIL vaccine (yeast). The nurse reported that the patient experienced muscle spasms after each of her HPV vaccine doses. It is not known when the spasms began or how long they lasted. At the time of the report the patient had recovered. The patient sought medical attention by phone. Additional information has been requested.


VAERS ID: 326127 (history)  
Form: Version 1.0  
Age: 24.0  
Sex: Female  
Location: California  
Vaccinated:2008-06-02
Onset:0000-00-00
Submitted: 2008-08-14
Entered: 2008-08-18
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 1 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Condition aggravated, Dizziness, Ophthalmological examination
SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (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? No
Previous Vaccinations:
Other Medications: ROZEREM
Current Illness: Sleep disorder, Dizziness
Preexisting Conditions: Pain
Allergies:
Diagnostic Lab Data: ophthalmological exam
CDC Split Type: WAES0807USA02252

Write-up: Information has been received from a physician concerning a 24 year old female healthcare worker with dizziness and sleep disorder and a history of pain who on 02-JUN-2008 was vaccinated with the first dose of GARDASIL vaccine (yeast). Concomitant therapy included ROZEREM. Subsequently, the patient experienced more severe dizziness after her first dose. The patient sought medical attention, saw a physician and had an eye check performed. At the time of reporting, the patient''s dizziness persisted. No additional AE information provided. Additional information has been requested.


VAERS ID: 326128 (history)  
Form: Version 1.0  
Age: 26.0  
Sex: Female  
Location: Unknown  
Vaccinated:0000-00-00
Onset:2007-08-01
Submitted: 2008-08-14
   Days after onset:379
Entered: 2008-08-18
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 3 UN / -

Administered by: Other       Purchased by: Other
Symptoms: Allergy test, Allergy to metals, Bacterial infection, Biopsy skin, Dyspnoea, Erythema, Rash generalised, Rash pruritic, Skin irritation
SMQs:, Anaphylactic reaction (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (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? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: Drug hypersensitivity, Spinal disorder
Preexisting Conditions: Spinal operation, Hospitalization
Allergies:
Diagnostic Lab Data: skin biopsy - ?/?/07 - punch hole biopsy inconclusive, diagnostic laboratory - ?/?/07 - touch test for nickel inconclusive
CDC Split Type: WAES0807USA02260

Write-up: Information has been received from a 26 year old female with an allergy to TYLENOL who in 2007 was vaccinated with the first dose of GARDASIL vaccine (yeast) prior to a spinal fusion surgery in August 2007. Two weeks after the surgery she broke out in a serious rash all over her body that was red, itchy and oozy. She went back to her surgeon who thought she may have caught a bacterial infection while in the hospital. After the treatment for that, the rash did not go away and patient was thought to have a staph infection. The rash was getting worse and she started having difficulty breathing and had to be taken to ER. It was determined she may have an allergic reaction to the nickel hardware that was placed in her spine. After that she was sent to an allergist who performed some tests, however the patient was taking allergy medication at the time and the test came back inconclusive. She did receive a second and third dose of GARDASIL vaccine (yeast) and was also scheduled for a second spinal fusion to replace the hardware with stainless steel. The patient is still experiencing a rash, that comes and goes depending on whether she puts the cream on it or not. She will bring the package insert for GARDASIL vaccine (yeast) with her to the allergist office to look at the ingredients and perform some tests to see if she could be allergic to any of the components. At time of report, the patient had not recovered from her rash. The outcome of the difficulty breathing, bacterial staph infection and allergic reaction to nickel hardware is unknown. No further information is available.


VAERS ID: 326129 (history)  
Form: Version 1.0  
Age: 19.0  
Sex: Female  
Location: Unknown  
Vaccinated:2008-06-20
Onset:2008-06-20
   Days after vaccination:0
Submitted: 2008-08-14
   Days after onset:55
Entered: 2008-08-18
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 1 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Hypersomnia
SMQs:, Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Depression (excl suicide and self injury) (broad)

Life Threatening? No
Birth Defect? No
Died? No
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:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: WAES0807USA02368

Write-up: Information has been received from a consumer, concerning her 19 years old daughter, who was vaccinated with the first dose of GARDASIL vaccine (yeast) (Lot #, site and route of administration not reported) in Jun 2008 (reported as "three weeks ago"). When the patient got the first injection she went home and immediately fell asleep for 15 hours. She was very worried about getting the shot before it happened. Additional information is not expected.


VAERS ID: 326130 (history)  
Form: Version 1.0  
Age: 18.0  
Sex: Female  
Location: Michigan  
Vaccinated:2008-03-14
Onset:2008-04-14
   Days after vaccination:31
Submitted: 2008-08-14
   Days after onset:122
Entered: 2008-08-18
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 1967U / 2 UN / IM

Administered by: Private       Purchased by: Private
Symptoms: Facial palsy
SMQs:, Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Hearing impairment (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? No
Previous Vaccinations:
Other Medications: hormonal contraceptives, ALEESE
Current Illness:
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: WAES0807USA02443

Write-up: Information has been received from a physician concerning an 18 year old female patient who on 14-JAN-2008 was vaccinated with the first dose of GARDASIL vaccine (yeast) (lot # 659653/1448U) and on 14-MAR-2008 was vaccinated with the second dose of GARDASIL vaccine (yeast) (lot # 660387/1967U). Concomitant therapy included hormonal contraceptives ALEESE. The physician reported that on 18-APR-2008, the patient developed Bell''s palsy after administration of two doses of HPV vaccine. The nurse reported that the patient was nit evaluated in her office. The patient was evaluated by her family physician. Subsequently, the patient recovered from BELL''S palsy. The patient sought medical attention via telephone. Additional information has been requested. No further information is available.


VAERS ID: 326131 (history)  
Form: Version 1.0  
Age: 19.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2008-07-09
Onset:2008-07-11
   Days after vaccination:2
Submitted: 2008-08-14
   Days after onset:34
Entered: 2008-08-18
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0070X / UNK UN / IM

Administered by: Other       Purchased by: Other
Symptoms: Blood magnesium decreased, Hypoaesthesia, Hypomagnesaemia, Nausea, Viral infection, Vomiting
SMQs:, Acute pancreatitis (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypokalaemia (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? No
Previous Vaccinations:
Other Medications: YAZ
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: serum magnesium - 07/11/08 - low
CDC Split Type: WAES0807USA02445

Write-up: Information has been received from a nurse concerning a 19 year old female who on 09-JUL-2008 was vaccinated with 0.5 ml of the first dose of GARDASIL vaccine (yeast) (lot # 660553/0070X) intramuscular. Concomitant therapy included drospirenone (+) ethinyl estradiol (YAZ). The Nurse reported that on 11-JUL-2008, the patient experienced nausea, vomiting, numbness throughout her body after receiving the dose of GARDASIL vaccine. The patient was brought to the emergency room were it was determinate that the symptoms were due to a virus and low magnesium level. Subsequently, the patient recovered from nausea, vomiting, numbness, virus infection and low magnesium level. Additional information has been requested.


VAERS ID: 326132 (history)  
Form: Version 1.0  
Age: 18.0  
Sex: Female  
Location: New York  
Vaccinated:2008-06-27
Onset:2008-07-04
   Days after vaccination:7
Submitted: 2008-08-14
   Days after onset:41
Entered: 2008-08-18
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / UNK UN / IM

Administered by: Other       Purchased by: Other
Symptoms: Abdominal pain upper, Blood test, Muscular weakness
SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CLONOPIN, PROZAC
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: WAES0807USA02449

Write-up: Information has been received from a consumer concerning to his daughter who on 27-JUN-2008 was vaccinated with 0.5 ml of GARDASIL vaccine (yeast) (batch and lot numbers not reported) intramuscular. Concomitant therapy included PROZAC and CLONOPIN. About a week after she got the vaccine (on approximately 04-JUL-2008) the patient experienced stomach pain and muscle weakness. The patient had blood work done (results not reported). The patient was recovering from stomach pain and muscle weakness. Additional information has been requested.


VAERS ID: 326134 (history)  
Form: Version 1.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2008-08-14
Entered: 2008-08-18
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Abdominal distension, Condition aggravated, Gastrointestinal disorder
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

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? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: Gastrointestinal disorder
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: WAES0807USA02456

Write-up: Information has been received from a registered nurse concerning her daughter with an unspecified gastrointestinal disorder who was vaccinated with GARDASIL vaccine (yeast) (Lot # not reported). The nurse reported that her daughter developed a worsening of a gastrointestinal disorder after receiving GARDASIL vaccine (yeast). The patient experienced increased abdominal bloating. The patient sought medical attention at physician''s office. At time of report, the patient''s gastrointestinal disorder and increased abdominal bloating persisted. Additional information has been requested.


VAERS ID: 326135 (history)  
Form: Version 1.0  
Age: 19.0  
Sex: Female  
Location: South Carolina  
Vaccinated:2007-09-07
Onset:2007-11-01
   Days after vaccination:55
Submitted: 2008-10-08
   Days after onset:342
Entered: 2008-08-18
   Days after submission:51
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 1448U / 3 UN / IM

Administered by: Unknown       Purchased by: Unknown
Symptoms: Blood test normal, Blood thyroid stimulating hormone normal, Cervical dysplasia, Dizziness, Echocardiogram abnormal, Electrocardiogram abnormal, Laboratory test normal, Mitral valve incompetence, Nausea, Sinus tachycardia, Smear cervix abnormal, Tricuspid valve incompetence
SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Supraventricular tachyarrhythmias (narrow), Reproductive premalignant disorders (narrow), Pulmonary hypertension (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Uterine and fallopian tube malignant tumours (broad), Dehydration (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? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Cervical dysplasia, Papanicolaou smear abnormal. PMH: None. On OCs.
Allergies:
Diagnostic Lab Data: cervical smear. Labs and Diagnostics: Chem, CBC and TSH WNL. EKG abnormal with non-specific ST changes-non acute. Echo with trace tricuspid and mitral regurg. EEG mildly abnormal with L temporal sharp transients. MRI brain WNL. cerviacal smear 06/??/2007 , abnormal PAP cervical dysplasia diagnostic laboratory 01??/2007, labs are negative
CDC Split Type: WAES0807USA02461

Write-up: Information has been received from a nurse concerning a 20 year old female with a history of cervical dysplasia and abnormal PAP, who in July 2007, was vaccinated with the first dose of GARDASIL vaccine (yeast). In September 2007, she was vaccinated with the second dose of GARDASIL vaccine (yeast) and in January 2008, she was vaccinated with the third dose of GARDASIL vaccine (yeast). The nurse reported that the patient developed persistent dizziness with occasional nausea after receiving the vaccine. The dizziness and nausea began in November 2007. The patient''s persistent dizziness and occasional nausea persisted. Additional information has been requested. 10/1/08 Office notes received from PCP. Pt presented 1/3/08 with c/o nausea and dizziness. Nausea began 11/07 and dizziness several weeks ago. Feels like sesation of passing out. Nausea is constant. PE WNL. Assessment: Gastritis, new. Dizziness, new. Nausea, new. Non-specific reaction to Tuberculin skin test w/o active TB, new. Tx with meds. Returned 6/25/08 with c/o worsening dizziness and lightheadedness which is interfering with QOL. Nausea improved. Weakness noted during pre-syncopal spells. Assessment: Dizziness, worsening. Nausea, stable. Plan to refer to cardiology, however office does not have consult name. 10/09/2008 Cardiology consult received for 7/7/2008 with Dx: Abnormal EKG. Dizziness and Giddiness. Syncope/Collapse. Disturbance of Vision. Nausea alone. PE (+) for flow murmur. Referred to ophth for black spots in visual field. Enc to increase salt intake. 11/03/2008 Neurology consult received dated 7/10/08. Pt reports ~6 month hx of dizziness, feeling like pt will faint w/o LOC. Brought on by standing quickly. PE WNL with BP drop from 100/80 to 96/80 with standing. This is in follow-up to report(s) previously submitted on 8/14/2008. Information has been received from a nurse concerning a 20 year old female with a history of cervical dyplasia and abnormal PA, who in July 2007, was vaccinated with the first dose of GARDASIL vaccine (yeast). In September 2007, she was vaccinated with the second dose of GARDASIL vaccine (yeast) and in January 2008, she was vaccinated with the third dose of GARDASIL vaccine (yeast). The nurse reported that the patient developed persistent dizziness with occasional nausea after receiving the vaccine. The patient had an unspecified blood test at primary physician''s office "within normal limits". The dizziness and nausea began in November 2007. The patient''s persistent dizziness and occasional nausea persieted. Follow up information was received froma aregistered nurse concerning a 20 year old female patient with mild dysplasia a nd no known allergies who on 05-JUL-2007 was vaccinated intramuscularly into the left buttock with a first dose of GARDASIL vaccine (yeast (Lot # 658100/0525UI. 0.5 ml on 07-SEP-2007 was vaccinated intramuscularly into the upper right arm with a second dose of GARDASIL vaccine(yeast) (Lot # 658558/1061U)0.5 ml and on 02-JAN-2008 was vaccinated intramuscularly into the upper left arm with a third dose of GARDASIL vaccine (yeast) (lot # 659653/1448U). Patient complained of nausea and dizziness for 11 months. Patient was dizzy all the time andnausea came occasionally. Patient saw primary care physician in January 2008 , all labs were negative. Patient saw cardiologist and neurologist. All was ngative (the results were not sent to the reporting physician''s office). The events reqired emergency room/doctor visit. At the time of reporting the patient had not receovered. There was no illness at the time of vaccination. Laboratory data: results not provided. No further information is available.


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