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This is VAERS ID 272610

History of Changes from the VAERS Wayback Machine

First Appeared on 12/31/2007

VAERS ID: 272610
Age:
Gender:Female
Location:Unknown
Vaccinated:2007-01-26
Onset:2007-01-26
Submitted:2007-02-14
Entered:2007-02-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 0 UN / -

Administered by: Other      Purchased by: Unknown
Symptoms: Pruritus, Rash

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

Write-up:Information has been received from a physician concerning a female patient who on 26-JAN-2007 was vaccinated with a first dose of Gardasil (yeast). On 26-JAN-2007 the patient experienced itching and a rash around the area of the arm and the back of the kn"ee. The rash continued to worsen and medication was ordered to treat the rash. At the time of this report, the patient''''s outcome was unknown. It was noted that the patient will not receive the second and third dose of the vaccine. No product quality comp


Changed on 12/8/2009

VAERS ID: 272610 Before After
Age:
Gender:Female
Location:Unknown
Vaccinated:2007-01-26
Onset:2007-01-26
Submitted:2007-02-14
Entered:2007-02-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 0 UN / -

Administered by: Other      Purchased by: Unknown Other
Symptoms: Pruritus, Rash

Life Threatening? No
Died? No
Permanent Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: UNK
Current Illness:
Preexisting Conditions: UNK
Diagnostic Lab Data: UNK
CDC 'Split Type': (blank) WAES0702USA00039

Write-up:Information has been received from a physician concerning a female patient who on 26-JAN-2007 was vaccinated with a first dose of Gardasil (yeast). On 26-JAN-2007 the patient experienced itching and a rash around the area of the arm and the back of the kn"ee. knee. The rash continued to worsen and medication was ordered to treat the rash. At the time of this report, the patient''''s patient''s outcome was unknown. It was noted that the patient will not receive the second and third dose of the vaccine. No product quality comp complaint was involved. Additional information has been requested.


Changed on 6/2/2010

VAERS ID: 272610 Before After
Age:
Gender:Female
Location:Unknown Georgia
Vaccinated:2007-01-26
Onset:2007-01-26
Submitted:2007-02-14
Entered:2007-02-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 0 UN / - UN

Administered by: Other      Purchased by: Other
Symptoms: Pruritus, Rash

Life Threatening? No
Died? No
Permanent Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: UNK
Current Illness:
Preexisting Conditions: UNK
Diagnostic Lab Data: UNK
CDC 'Split Type': WAES0702USA00039

Write-up:Information has been received from a physician concerning a female patient who on 26-JAN-2007 was vaccinated with a first dose of Gardasil (yeast). On 26-JAN-2007 the patient experienced itching and a rash around the area of the arm and the back of the knee. The rash continued to worsen and medication was ordered to treat the rash. At the time of this report, the patient''s outcome was unknown. It was noted that the patient will not receive the second and third dose of the vaccine. No product quality complaint was involved. Additional information has been requested. This is in follow-up to report (s) previously submitted on 2/14/2007. Information has been receivced from a physician concerning a female patient who on 26-JAN-2007 was vaccinated with a first dose of GARDASIL. On 26-JAN-2007 the patient experienced itching and a rash around the area of the arm and the back of the knee. The nurse stated that the rash began in the crevices of the elbows and knees and progressed to other parts of the body before the medicine was ordered to stop the itching. The rash continued to worsen and medication was ordered to treat the rash. At the time of this report, the patient''s outcome was unknown. It was noted that the patient will not receive the second and third dose of the vaccine. No product quality complaint was involved. Additional information has been requested.


Changed on 6/14/2014

VAERS ID: 272610 Before After
Age:
Gender:Female
Location:Georgia
Vaccinated:2007-01-26
Onset:2007-01-26
Submitted:2007-02-14
Entered:2007-02-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 0 UN / UN

Administered by: Other      Purchased by: Other
Symptoms: Pruritus, Rash

Life Threatening? No
Died? No
Permanent Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: UNK
Current Illness:
Preexisting Conditions: UNK
Diagnostic Lab Data: UNK
CDC 'Split Type': WAES0702USA00039

Write-up:Information has been received from a physician concerning a female patient who on 26-JAN-2007 was vaccinated with a first dose of Gardasil (yeast). On 26-JAN-2007 the patient experienced itching and a rash around the area of the arm and the back of the knee. The rash continued to worsen and medication was ordered to treat the rash. At the time of this report, the patient''s outcome was unknown. It was noted that the patient will not receive the second and third dose of the vaccine. No product quality complaint was involved. Additional information has been requested. This is in follow-up to report (s) previously submitted on 2/14/2007. Information has been receivced from a physician concerning a female patient who on 26-JAN-2007 was vaccinated with a first dose of GARDASIL. On 26-JAN-2007 the patient experienced itching and a rash around the area of the arm and the back of the knee. The nurse stated that the rash began in the crevices of the elbows and knees and progressed to other parts of the body before the medicine was ordered to stop the itching. The rash continued to worsen and medication was ordered to treat the rash. At the time of this report, the patient''s outcome was unknown. It was noted that the patient will not receive the second and third dose of the vaccine. No product quality complaint was involved. Additional information has been requested.


Changed on 5/14/2017

VAERS ID: 272610 Before After
Age:
Gender:Female
Location:Georgia
Vaccinated:2007-01-26
Onset:2007-01-26
Submitted:2007-02-14
Entered:2007-02-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 0 UN / UN

Administered by: Other      Purchased by: Other
Symptoms: Pruritus, Rash

Life Threatening? No
Died? No
Permanent Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: UNK
Current Illness:
Preexisting Conditions: UNK
Diagnostic Lab Data: UNK
CDC 'Split Type': WAES0702USA00039

Write-up:Information has been received from a physician concerning a female patient who on 26-JAN-2007 was vaccinated with a first dose of Gardasil (yeast). On 26-JAN-2007 the patient experienced itching and a rash around the area of the arm and the back of the knee. The rash continued to worsen and medication was ordered to treat the rash. At the time of this report, the patient''s outcome was unknown. It was noted that the patient will not receive the second and third dose of the vaccine. No product quality complaint was involved. Additional information has been requested. This is in follow-up to report (s) previously submitted on 2/14/2007. Information has been receivced from a physician concerning a female patient who on 26-JAN-2007 was vaccinated with a first dose of GARDASIL. On 26-JAN-2007 the patient experienced itching and a rash around the area of the arm and the back of the knee. The nurse stated that the rash began in the crevices of the elbows and knees and progressed to other parts of the body before the medicine was ordered to stop the itching. The rash continued to worsen and medication was ordered to treat the rash. At the time of this report, the patient''s outcome was unknown. It was noted that the patient will not receive the second and third dose of the vaccine. No product quality complaint was involved. Additional information has been requested.


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