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Found 18461 events where Vaccine is HPV4

Event Details Report

This is page 1017 out of 1847

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VAERS ID:326376  Vaccinated:2008-07-03
Age:24.0  Onset:2008-07-13, Days after vaccination: 10
Gender:Female  Submitted:2008-08-14, Days after onset: 32
Location:Colorado  Entered:2008-08-18, Days after submission: 4
Life Threatening Illness? No
Died? No
Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Current Illness: Sulfonamide allergy
Diagnostic Lab Data: urinalysis - 07/13/08 - negative
Previous Vaccinations:
Other Medications: None
Preexisting Conditions:
CDC 'Split Type': WAES0807USA03833
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4MERCK & CO. INC. 0UNUN
Administered by: Other     Purchased by: Other
Symptoms: Abdominal pain upper, Back pain, Dysuria, Fatigue, Headache, Menstruation irregular, Urine analysis normal
Write-up: Information has been received from a consumer concerning her 24 year old daughter with sulfonamide allergy and no relevant medical history who on 03-JUL-2008 was vaccinated with a first dose of GARDASIL vaccine (yeast) (lot number, injection site and route not reported). There was no concomitant medication. On 13-JUL-2008 the patient experienced stomach cramps, back pain, extreme fatigue, pain upon urination, headaches and irregular menstrual cycles. Unspecified medical attention was sought. The patient's events persisted. Additional information has been requested.

VAERS ID:326377  Vaccinated:2008-06-24
Age:16.0  Onset:2008-06-24, Days after vaccination: 0
Gender:Female  Submitted:2008-08-14, Days after onset: 51
Location:North Carolina  Entered:2008-08-18, Days after submission: 4
Life Threatening Illness? No
Died? No
Disability? No
Recovered? Yes
ER or Doctor Visit? Yes
Hospitalized? No
Current Illness:
Diagnostic Lab Data: Unknown
Previous Vaccinations:
Other Medications: None
Preexisting Conditions: Unknown
CDC 'Split Type': WAES0807USA03836
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4MERCK & CO. INC. 0UNUN
Administered by: Other     Purchased by: Other
Symptoms: Syncope
Write-up: Information has been received from a registered nurse concerning a 16 female who on 24-JUN-2008 was vaccinated with the first dose of GARDASIL vaccine (yeast). There was no concomitant medication. On 24-JUN-2008 the patient experienced faint after vaccination. The patient then revived and then fainted again within a short time while still in office. The patient recovered from faint after vaccination before leaving the office on 24-JUN-2008. Additional information has been requested.

VAERS ID:326378  Vaccinated:2008-05-30
Age:14.0  Onset:2008-06-01, Days after vaccination: 2
Gender:Female  Submitted:2008-08-14, Days after onset: 74
Location:Kansas  Entered:2008-08-18, Days after submission: 4
Life Threatening Illness? No
Died? No
Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Current Illness: Mood swings, Acne, Asthma
Diagnostic Lab Data: None
Previous Vaccinations:
Other Medications: albuterol, TRIAZ, RETIN-A MICRO GEL
Preexisting Conditions: Irregular periods
CDC 'Split Type': WAES0807USA03846
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4MERCK & CO. INC.1757U0IMUN
Administered by: Other     Purchased by: Other
Symptoms: Abdominal distension, Amenorrhoea, Anger, Irritability, Mood altered
Write-up: Information has been received from a physician concerning a 14 year old white female with menarche in February 2008 and irregular periods. The patient had asthma, acne and mood swings for which she was seen by a counselor prior to vaccination who on 30-MAY-2008 was vaccinated intramuscularly with the first 0.5 ml dose of GARDASIL vaccine (yeast) (lot no. 659182/1757U). Concomitant therapy included albuterol, benzoyl peroxide (TRIAZ) and RETIN-A MICRO GEL. On approximately 01-JUN-2008 (within the first week after the vaccination) the patient experienced anger outbursts, irritability, moodiness and bloating. The patient stated that she did not have a period in June 2008 but experienced bloating, moodiness and anger outburst off and on. She went on to have a menstrual period on 09-JUL-2008. The physician confirmed that the patient was not pregnant. On 16-JUL-2008, the patient was seen by the physician for the symptoms. The patient was asymptomatic at the visit. The patient was in counseling and the counselor stated that she felt mood problems were probably related to her vaccination. The patient's symptoms were noted to occur "on and off". This is one of several reports from the same source. Additional information has been requested.

VAERS ID:326379  Vaccinated:2008-07-17
Age:16.0  Onset:2008-07-17, Days after vaccination: 0
Gender:Female  Submitted:2008-08-14, Days after onset: 28
Location:Pennsylvania  Entered:2008-08-18, Days after submission: 4
Life Threatening Illness? No
Died? No
Disability? No
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Current Illness:
Diagnostic Lab Data: None
Previous Vaccinations:
Other Medications: None
Preexisting Conditions: None
CDC 'Split Type': WAES0807USA03852
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4MERCK & CO. INC.0755U1IMLA
Administered by: Private     Purchased by: Private
Symptoms: Dizziness, Fatigue, Hypotension, Syncope
Write-up: Information has been received from a physician concerning a 16 year old female who on 17-JUL-2008 was vaccinated intramuscularly with the second 0.5 ml dose of GARDASIL vaccine (yeast) (lot no. 658219/0755U). After receiving the second dose the patient fainted in the parking lot of the physician's office. The patient was taken back to the office for observation. Subsequently, on the same day, the patient was recovered. Additional information has been requested. 10/08/08 This is in follow-up to report(s) previously submitted on 8/14/2008. Initial information has been received from a physician and follow-up information was received from a medical assistant concerning a 16 year old female with no known allergies who on 17-JUL-2008 at 11:15 AM was vaccinated intramuscularly with the second 0.5 ml dose of GARDASIL (lot no. 658219/0755U) into the left arm. After receiving the second dose, at 11:45 AM, the patient fainted in the parking lot of the physician's office. The patient was taken back to the office for observation. The patient experienced vasovagal syncope, very lightheaded and low blood pressure. After 15 minutes, the patient was stable but she was tired when she left the office. Subsequently, on the same day, the patient was recovered. Additional information is not expected.

VAERS ID:326380  Vaccinated:0000-00-00
Age:22.0  Onset:0000-00-00
Gender:Female  Submitted:2008-08-14
Location:Nebraska  Entered:2008-08-18, Days after submission: 4
Life Threatening Illness? No
Died? No
Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Current Illness:
Diagnostic Lab Data: Unknown
Previous Vaccinations:
Other Medications: Unknown
Preexisting Conditions: Unknown
CDC 'Split Type': WAES0807USA03853
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4MERCK & CO. INC. 0UNUN
Administered by: Other     Purchased by: Other
Symptoms: Fungal infection, Vaccine positive rechallenge
Write-up: Information has been received from a nurse concerning a 22 year old female who on unspecified dates was vaccinated with 2 doses of GARDASIL vaccine (yeast). After the first vaccination, the patient developed yeast infection. After the second vaccination the patient developed another yeast infection. As of 18-JUL-2008, the patient was not recovered. The patient saw a doctor. Additional information has been requested.

VAERS ID:326470  Vaccinated:2008-07-25
Age:19.0  Onset:2008-07-25, Days after vaccination: 0
Gender:Female  Submitted:2008-08-14, Days after onset: 20
Location:Unknown  Entered:2008-08-18, Days after submission: 4
Life Threatening Illness? No
Died? No
Disability? No
Recovered? No
ER or Doctor Visit? No
Hospitalized? No
Current Illness:
Diagnostic Lab Data: Unknown
Previous Vaccinations:
Other Medications: Unknown
Preexisting Conditions: Unknown
CDC 'Split Type': WAES0807USA05717
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4MERCK & CO. INC. 0IMUN
Administered by: Other     Purchased by: Other
Symptoms: Nausea
Write-up: Information has been received from a nurse concerning a 19 year old female who on 25-JUL-2008 was vaccinated intramuscularly with the first 0.5 ml dose of GARDASIL vaccine (yeast). The nurse reported that on 30-JUL-2008, "today", the mother called the office and reported that her daughter had been nauseous since receiving the first dose. At the time of this report, the patient was still nauseous. The patient's mother called the office to seek unspecified medical attention. Additional information has been requested.

VAERS ID:326471  Vaccinated:2008-07-28
Age:18.0  Onset:2008-07-29, Days after vaccination: 1
Gender:Female  Submitted:2008-08-14, Days after onset: 16
Location:Indiana  Entered:2008-08-18, Days after submission: 4
Life Threatening Illness? No
Died? No
Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Current Illness:
Diagnostic Lab Data: None
Previous Vaccinations:
Other Medications: None
Preexisting Conditions: None
CDC 'Split Type': WAES0807USA05728
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4MERCK & CO. INC. 0UNUN
Administered by: Other     Purchased by: Other
Symptoms: Erythema, Fatigue, Pain, Rash
Write-up: Information has been received from a physician concerning an 18 year old female with no relevant medical history or allergies who on 28-JUL-2008 was vaccinated with a first dose of GARDASIL vaccine (yeast). There was no concomitant medication. On 29-JUL-2008, also reported as "24 hours after vaccination" the patient developed fatigue and a rash on the palms of the hands and the soles of the feet. On 30-JUL-2008, the patient sought treatment with an urgent care provider rather than the provider who administered the vaccine. The rash was described as "little reddened spots that were almost raised and similar in look to that of a hands foot and mouth disease rash". The rash was painful and did not itch. The physician planed to prescribe unspecified anti-inflammatory pain medication for the symptoms. At the time of reporting, the patient's events persisted. Additional information has been requested.

VAERS ID:326472  Vaccinated:2007-07-27
Age:18.0  Onset:2007-07-27, Days after vaccination: 0
Gender:Female  Submitted:2008-08-14, Days after onset: 384
Location:Illinois  Entered:2008-08-18, Days after submission: 4
Life Threatening Illness? No
Died? No
Disability? No
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Current Illness:
Diagnostic Lab Data: None
Previous Vaccinations:
Other Medications:
Preexisting Conditions: Unknown
CDC 'Split Type': WAES0807USA05729
Vaccination
Manufacturer
Lot
Dose
Route
Site
DTPUNKNOWN MANUFACTURER  UNUN
HPV4MERCK & CO. INC. 0UNUN
Administered by: Other     Purchased by: Other
Symptoms: Dizziness, Pain in extremity
Write-up: Information has been received from an office manager concerning an 18 year old female who on 27-JUL-2007 was vaccinated with the first dose of GARDASIL vaccine (yeast). After receiving the first dose, the patient's arm was sore. On 29-JUL-2008 the patient came back to the office and was vaccinated with the second dose of GARDASIL vaccine (yeast), which was almost a year later. Concomitant therapy included diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid. On the same day, after receiving the second dose, the patient was a little dizzy so she waited for a while until she felt better. The patient was fully recovered on that day. The patient sought unspecified medical attention. Additional information has been requested.

VAERS ID:326473  Vaccinated:2008-07-30
Age:18.0  Onset:2008-07-30, Days after vaccination: 0
Gender:Female  Submitted:2008-08-14, Days after onset: 15
Location:North Carolina  Entered:2008-08-18, Days after submission: 4
Life Threatening Illness? No
Died? No
Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Current Illness:
Diagnostic Lab Data: None
Previous Vaccinations:
Other Medications: None
Preexisting Conditions: None
CDC 'Split Type': WAES0807USA05736
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4MERCK & CO. INC.1740U3IMUN
Administered by: Other     Purchased by: Other
Symptoms: Inappropriate schedule of drug administration, Pain in extremity
Write-up: Information has been received from a medical assistant concerning an 18 year old female with no pertinent medical history or drug reactions or allergies who on 01-NOV-2006 was vaccinated with the first dose of GARDSIL vaccine (yeast) (lot no. 653978/0955F). On 11-JAN-2007 the patient was vaccinated with the second dose of GARDASIL vaccine (yeast) (lot no. 654389/0961F). On an unspecified date, the patient was vaccinated with the third dose of GARDASIL vaccine (yeast). On 30-JUL-2008 the patient was vaccinated intramuscularly with the fourth 0.5 ml dose of GARDASIL vaccine (yeast) (lot no. 659962/1740U) and experienced a sore arm (which arm unspecified). There was no concomitant medication. It was not documented in the patient's record that a third dose was given however the mother of the patient insist she had received the third dose. At the time of this report, the patient was recovering from a sore arm. The patient sought unspecified medical attention in the office. Additional information has been requested.

VAERS ID:326474  Vaccinated:2008-01-01
Age:  Onset:2008-01-01, Days after vaccination: 0
Gender:  Submitted:2008-08-14, Days after onset: 225
Location:Unknown  Entered:2008-08-18, Days after submission: 4
Life Threatening Illness? No
Died? No
Disability? No
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Current Illness:
Diagnostic Lab Data: Unknown
Previous Vaccinations:
Other Medications: Unknown
Preexisting Conditions: Unknown
CDC 'Split Type': WAES0807USA05737
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4MERCK & CO. INC. 0IMUN
Administered by: Other     Purchased by: Other
Symptoms: Injection site mass
Write-up: Information has been received from a physician's assistant concerning a patient who in approximately January 2008, "7 months ago", was vaccinated with the first dose of GARDASIL vaccine (yeast). On the same day, "shortly after the first dose was given", the patient developed a "knot" at the injection site. The patient had since been given the next 2 doses and had not reported any adverse reactions. On an unspecified date the patient recovered from a "knot" at the injection site. The patient contacted the physician's office and sought unspecified medical attention. Additional information has been requested.

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