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This is VAERS ID 429262

History of Changes from the VAERS Wayback Machine

First Appeared on 8/12/2011

VAERS ID: 429262
Age:
Gender:Female
Location:Unknown
Vaccinated:2011-02-01
Onset:0000-00-00
Submitted:2011-08-04
Entered:2011-08-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 0 AR / UN

Administered by: Other      Purchased by: Other
Symptoms: Injection site pain, Injection site swelling, Injected limb mobility decreased

Life Threatening? No
Died? No
Permanent Disability? Yes
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES1104USA01919

Write-up:Information has been received from a physician''s assistant concerning a female patient who in approximately February 2011 ("around two months ago"), was vaccinated with a first 0.5 ml dose of GARDASIL. Subsequently the patient said her arm where the injection was given, it swelled up and she had a lot of pain about 5 days around the injection site. The swelling continued for days as well. She had limited use in her arm because of the swelling. It was reported after 5 days the adverse events improved. The patient did not want to continue the second and third dose. At the time of reporting, the patient was fine. The patient did not seek medical attention. The "arm where the injection was given, swelled up" was considered to be disabling ("She had limited use in her arm because of the swelling"). No further information is available.


Changed on 6/14/2014

VAERS ID: 429262 Before After
Age:
Gender:Female
Location:Unknown
Vaccinated:2011-02-01
Onset:0000-00-00
Submitted:2011-08-04
Entered:2011-08-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 0 AR / UN

Administered by: Other      Purchased by: Other
Symptoms: Injection site pain, Injection site swelling, Injected limb mobility decreased

Life Threatening? No
Died? No
Permanent Disability? Yes
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES1104USA01919

Write-up:Information has been received from a physician''s assistant concerning a female patient who in approximately February 2011 ("around two months ago"), was vaccinated with a first 0.5 ml dose of GARDASIL. Subsequently the patient said her arm where the injection was given, it swelled up and she had a lot of pain about 5 days around the injection site. The swelling continued for days as well. She had limited use in her arm because of the swelling. It was reported after 5 days the adverse events improved. The patient did not want to continue the second and third dose. At the time of reporting, the patient was fine. The patient did not seek medical attention. The "arm where the injection was given, swelled up" was considered to be disabling ("She had limited use in her arm because of the swelling"). No further information is available.


Changed on 4/14/2017

VAERS ID: 429262 Before After
Age:
Gender:Female
Location:Unknown
Vaccinated:2011-02-01
Onset:0000-00-00
Submitted:2011-08-04
Entered:2011-08-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 0 AR / UN

Administered by: Other      Purchased by: Other
Symptoms: Injection site pain, Injection site swelling, Injected limb mobility decreased

Life Threatening? No
Died? No
Permanent Disability? Yes
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES1104USA01919

Write-up:Information has been received from a physician''s assistant concerning a female patient who in approximately February 2011 ("around two months ago"), was vaccinated with a first 0.5 ml dose of GARDASIL. Subsequently the patient said her arm where the injection was given, it swelled up and she had a lot of pain about 5 days around the injection site. The swelling continued for days as well. She had limited use in her arm because of the swelling. It was reported after 5 days the adverse events improved. The patient did not want to continue the second and third dose. At the time of reporting, the patient was fine. The patient did not seek medical attention. The "arm where the injection was given, swelled up" was considered to be disabling ("She had limited use in her arm because of the swelling"). No further information is available.


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http://www.medalerts.org/vaersdb/findfield.php?IDNUMBER=429262&WAYBACKHISTORY=ON


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