National Vaccine
Information Center

Your Health. Your Family. Your Choice.

MedAlerts Home
Search Results

This is VAERS ID 497405

History of Changes from the VAERS Wayback Machine

First Appeared on 11/13/2013

VAERS ID: 497405
VAERS Form:
Age:14.0
Sex:Female
Location:Foreign
Vaccinated:2011-07-01
Onset:0000-00-00
Submitted:2013-07-22
Entered:2013-07-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV2: HPV (CERVARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 0 UN / IM

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Arthralgia, Back pain, Chest pain, Depressed level of consciousness, Depression, Dermatitis, Diarrhoea, Dizziness, Dyspnoea exertional, Headache, Hypersomnia, Hyperventilation, Malaise, Mental impairment, Oedema peripheral, Pain in extremity, Palpitations, Parotitis, Pyrexia, Stomatitis, Urticaria, Vomiting, Abulia, Injection site swelling, Decreased appetite, Vaccine positive rechallenge

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: UNK
CDC 'Split Type': B0908384A

Write-up: This case was reported by a physician and described the occurrence of swelling injection site in a 14-year-old female subject who was vaccinated with CERVARIX (GlaxoSmithKline). In July 2011, the subject received 1st dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the first vaccination, the subject experienced injection site swelling, pyrexia, headache, and urticaria. The symptoms subsided in approximately 1 week, but headache and urticaria lasted 2 weeks. In October 2011, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). Within one month after 2nd dose of vaccine, the subject experienced the same symptoms as those after the first vaccination except urticaria. She also experienced malaise. One month after the second vaccination, the subject also experienced stomatitis, pyrexia, diarrhoea, abdominal pain, and dermatitis developed, and 2 months after vaccination, severe urticaria developed. In March 2012, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the third vaccination, the subject experienced arthralgia along with the same symptoms as those experienced after the second vaccination. Fourteen days after the vaccination, exertional dyspnoea and severe malaise were also developed. One month and a half after the vaccination, urticaria, pain in the lower and upper extremities, dermatitis, and stomatitis developed. Stomatitis, dermatitis, malaise, low back pain, slight fever, arthralgia, abdominal pain, and headache were developed and lasted for 2 or 3 months after vaccination. Hyperpnoea and a feeling of dyspnoea were also experienced even at rest as well as pedal oedema. Three to five months after the third vaccination, the subject experienced generalised joint pains, abdominal pain, headache, multiple stomatitis, inappetence, vomiting, slight fever, and parotitis. Six to nine months after the third vaccination, she experienced abnormal malaise, clouding of consciousness, anterior chest pain similar to angina pectoris and palpitations also developed. In addition, giddiness and excessive sleep were developed. The physician considered the events were clinically significant (or requiring intervention). Approximately 10 months after the third vaccination, the chest pain was resolved but replaced by hyperpnoea. Although the pain in the body improved, the subject still experienced fatigue, hypobulia, and reduced thinking. It was considered that the subject had depressive symptoms. The outcome of the rest of the events was unspecified.


Changed on 9/14/2017

VAERS ID: 497405 Before After
VAERS Form:(blank) 1
Age:14.0
Sex:Female
Location:Foreign
Vaccinated:2011-07-01
Onset:0000-00-00
Submitted:2013-07-22
Entered:2013-07-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV2: HPV (CERVARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 0 1 UN / IM

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Arthralgia, Back pain, Chest pain, Depressed level of consciousness, Depression, Dermatitis, Diarrhoea, Dizziness, Dyspnoea exertional, Headache, Hypersomnia, Hyperventilation, Malaise, Mental impairment, Oedema peripheral, Pain in extremity, Palpitations, Parotitis, Pyrexia, Stomatitis, Urticaria, Vomiting, Abulia, Injection site swelling, Decreased appetite, Vaccine positive rechallenge

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: UNK
CDC 'Split Type': B0908384A

Write-up: This case was reported by a physician and described the occurrence of swelling injection site in a 14-year-old female subject who was vaccinated with CERVARIX (GlaxoSmithKline). In July 2011, the subject received 1st dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the first vaccination, the subject experienced injection site swelling, pyrexia, headache, and urticaria. The symptoms subsided in approximately 1 week, but headache and urticaria lasted 2 weeks. In October 2011, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). Within one month after 2nd dose of vaccine, the subject experienced the same symptoms as those after the first vaccination except urticaria. She also experienced malaise. One month after the second vaccination, the subject also experienced stomatitis, pyrexia, diarrhoea, abdominal pain, and dermatitis developed, and 2 months after vaccination, severe urticaria developed. In March 2012, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the third vaccination, the subject experienced arthralgia along with the same symptoms as those experienced after the second vaccination. Fourteen days after the vaccination, exertional dyspnoea and severe malaise were also developed. One month and a half after the vaccination, urticaria, pain in the lower and upper extremities, dermatitis, and stomatitis developed. Stomatitis, dermatitis, malaise, low back pain, slight fever, arthralgia, abdominal pain, and headache were developed and lasted for 2 or 3 months after vaccination. Hyperpnoea and a feeling of dyspnoea were also experienced even at rest as well as pedal oedema. Three to five months after the third vaccination, the subject experienced generalised joint pains, abdominal pain, headache, multiple stomatitis, inappetence, vomiting, slight fever, and parotitis. Six to nine months after the third vaccination, she experienced abnormal malaise, clouding of consciousness, anterior chest pain similar to angina pectoris and palpitations also developed. In addition, giddiness and excessive sleep were developed. The physician considered the events were clinically significant (or requiring intervention). Approximately 10 months after the third vaccination, the chest pain was resolved but replaced by hyperpnoea. Although the pain in the body improved, the subject still experienced fatigue, hypobulia, and reduced thinking. It was considered that the subject had depressive symptoms. The outcome of the rest of the events was unspecified.


Changed on 2/14/2018

VAERS ID: 497405 Before After
VAERS Form:1
Age:14.0
Sex:Female
Location:Foreign
Vaccinated:2011-07-01
Onset:0000-00-00
Submitted:2013-07-22
Entered:2013-07-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV2: HPV (CERVARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 UN / IM

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Arthralgia, Back pain, Chest pain, Depressed level of consciousness, Depression, Dermatitis, Diarrhoea, Dizziness, Dyspnoea exertional, Headache, Hypersomnia, Hyperventilation, Malaise, Mental impairment, Oedema peripheral, Pain in extremity, Palpitations, Parotitis, Pyrexia, Stomatitis, Urticaria, Vomiting, Abulia, Injection site swelling, Decreased appetite, Vaccine positive rechallenge

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: UNK
CDC 'Split Type': B0908384A

Write-up: This case was reported by a physician and described the occurrence of swelling injection site in a 14-year-old female subject who was vaccinated with CERVARIX (GlaxoSmithKline). In July 2011, the subject received 1st dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the first vaccination, the subject experienced injection site swelling, pyrexia, headache, and urticaria. The symptoms subsided in approximately 1 week, but headache and urticaria lasted 2 weeks. In October 2011, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). Within one month after 2nd dose of vaccine, the subject experienced the same symptoms as those after the first vaccination except urticaria. She also experienced malaise. One month after the second vaccination, the subject also experienced stomatitis, pyrexia, diarrhoea, abdominal pain, and dermatitis developed, and 2 months after vaccination, severe urticaria developed. In March 2012, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the third vaccination, the subject experienced arthralgia along with the same symptoms as those experienced after the second vaccination. Fourteen days after the vaccination, exertional dyspnoea and severe malaise were also developed. One month and a half after the vaccination, urticaria, pain in the lower and upper extremities, dermatitis, and stomatitis developed. Stomatitis, dermatitis, malaise, low back pain, slight fever, arthralgia, abdominal pain, and headache were developed and lasted for 2 or 3 months after vaccination. Hyperpnoea and a feeling of dyspnoea were also experienced even at rest as well as pedal oedema. Three to five months after the third vaccination, the subject experienced generalised joint pains, abdominal pain, headache, multiple stomatitis, inappetence, vomiting, slight fever, and parotitis. Six to nine months after the third vaccination, she experienced abnormal malaise, clouding of consciousness, anterior chest pain similar to angina pectoris and palpitations also developed. In addition, giddiness and excessive sleep were developed. The physician considered the events were clinically significant (or requiring intervention). Approximately 10 months after the third vaccination, the chest pain was resolved but replaced by hyperpnoea. Although the pain in the body improved, the subject still experienced fatigue, hypobulia, and reduced thinking. It was considered that the subject had depressive symptoms. The outcome of the rest of the events was unspecified.


Changed on 6/14/2018

VAERS ID: 497405 Before After
VAERS Form:1
Age:14.0
Sex:Female
Location:Foreign
Vaccinated:2011-07-01
Onset:0000-00-00
Submitted:2013-07-22
Entered:2013-07-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV2: HPV (CERVARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 UN / IM

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Arthralgia, Back pain, Chest pain, Depressed level of consciousness, Depression, Dermatitis, Diarrhoea, Dizziness, Dyspnoea exertional, Headache, Hypersomnia, Hyperventilation, Malaise, Mental impairment, Oedema peripheral, Pain in extremity, Palpitations, Parotitis, Pyrexia, Stomatitis, Urticaria, Vomiting, Abulia, Injection site swelling, Decreased appetite, Vaccine positive rechallenge

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: UNK
CDC 'Split Type': B0908384A

Write-up: This case was reported by a physician and described the occurrence of swelling injection site in a 14-year-old female subject who was vaccinated with CERVARIX (GlaxoSmithKline). In July 2011, the subject received 1st dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the first vaccination, the subject experienced injection site swelling, pyrexia, headache, and urticaria. The symptoms subsided in approximately 1 week, but headache and urticaria lasted 2 weeks. In October 2011, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). Within one month after 2nd dose of vaccine, the subject experienced the same symptoms as those after the first vaccination except urticaria. She also experienced malaise. One month after the second vaccination, the subject also experienced stomatitis, pyrexia, diarrhoea, abdominal pain, and dermatitis developed, and 2 months after vaccination, severe urticaria developed. In March 2012, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the third vaccination, the subject experienced arthralgia along with the same symptoms as those experienced after the second vaccination. Fourteen days after the vaccination, exertional dyspnoea and severe malaise were also developed. One month and a half after the vaccination, urticaria, pain in the lower and upper extremities, dermatitis, and stomatitis developed. Stomatitis, dermatitis, malaise, low back pain, slight fever, arthralgia, abdominal pain, and headache were developed and lasted for 2 or 3 months after vaccination. Hyperpnoea and a feeling of dyspnoea were also experienced even at rest as well as pedal oedema. Three to five months after the third vaccination, the subject experienced generalised joint pains, abdominal pain, headache, multiple stomatitis, inappetence, vomiting, slight fever, and parotitis. Six to nine months after the third vaccination, she experienced abnormal malaise, clouding of consciousness, anterior chest pain similar to angina pectoris and palpitations also developed. In addition, giddiness and excessive sleep were developed. The physician considered the events were clinically significant (or requiring intervention). Approximately 10 months after the third vaccination, the chest pain was resolved but replaced by hyperpnoea. Although the pain in the body improved, the subject still experienced fatigue, hypobulia, and reduced thinking. It was considered that the subject had depressive symptoms. The outcome of the rest of the events was unspecified.


Changed on 8/14/2018

VAERS ID: 497405 Before After
VAERS Form:1
Age:14.0
Sex:Female
Location:Foreign
Vaccinated:2011-07-01
Onset:0000-00-00
Submitted:2013-07-22
Entered:2013-07-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV2: HPV (CERVARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 UN / IM

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Arthralgia, Back pain, Chest pain, Depressed level of consciousness, Depression, Dermatitis, Diarrhoea, Dizziness, Dyspnoea exertional, Headache, Hypersomnia, Hyperventilation, Malaise, Mental impairment, Oedema peripheral, Pain in extremity, Palpitations, Parotitis, Pyrexia, Stomatitis, Urticaria, Vomiting, Abulia, Injection site swelling, Decreased appetite, Vaccine positive rechallenge

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: UNK
CDC 'Split Type': B0908384A

Write-up: This case was reported by a physician and described the occurrence of swelling injection site in a 14-year-old female subject who was vaccinated with CERVARIX (GlaxoSmithKline). In July 2011, the subject received 1st dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the first vaccination, the subject experienced injection site swelling, pyrexia, headache, and urticaria. The symptoms subsided in approximately 1 week, but headache and urticaria lasted 2 weeks. In October 2011, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). Within one month after 2nd dose of vaccine, the subject experienced the same symptoms as those after the first vaccination except urticaria. She also experienced malaise. One month after the second vaccination, the subject also experienced stomatitis, pyrexia, diarrhoea, abdominal pain, and dermatitis developed, and 2 months after vaccination, severe urticaria developed. In March 2012, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the third vaccination, the subject experienced arthralgia along with the same symptoms as those experienced after the second vaccination. Fourteen days after the vaccination, exertional dyspnoea and severe malaise were also developed. One month and a half after the vaccination, urticaria, pain in the lower and upper extremities, dermatitis, and stomatitis developed. Stomatitis, dermatitis, malaise, low back pain, slight fever, arthralgia, abdominal pain, and headache were developed and lasted for 2 or 3 months after vaccination. Hyperpnoea and a feeling of dyspnoea were also experienced even at rest as well as pedal oedema. Three to five months after the third vaccination, the subject experienced generalised joint pains, abdominal pain, headache, multiple stomatitis, inappetence, vomiting, slight fever, and parotitis. Six to nine months after the third vaccination, she experienced abnormal malaise, clouding of consciousness, anterior chest pain similar to angina pectoris and palpitations also developed. In addition, giddiness and excessive sleep were developed. The physician considered the events were clinically significant (or requiring intervention). Approximately 10 months after the third vaccination, the chest pain was resolved but replaced by hyperpnoea. Although the pain in the body improved, the subject still experienced fatigue, hypobulia, and reduced thinking. It was considered that the subject had depressive symptoms. The outcome of the rest of the events was unspecified.


Changed on 9/14/2018

VAERS ID: 497405 Before After
VAERS Form:1
Age:14.0
Sex:Female
Location:Foreign
Vaccinated:2011-07-01
Onset:0000-00-00
Submitted:2013-07-22
Entered:2013-07-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV2: HPV (CERVARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 UN / IM

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Arthralgia, Back pain, Chest pain, Depressed level of consciousness, Depression, Dermatitis, Diarrhoea, Dizziness, Dyspnoea exertional, Headache, Hypersomnia, Hyperventilation, Malaise, Mental impairment, Oedema peripheral, Pain in extremity, Palpitations, Parotitis, Pyrexia, Stomatitis, Urticaria, Vomiting, Abulia, Injection site swelling, Decreased appetite, Vaccine positive rechallenge

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: UNK
CDC 'Split Type': B0908384A

Write-up: This case was reported by a physician and described the occurrence of swelling injection site in a 14-year-old female subject who was vaccinated with CERVARIX (GlaxoSmithKline). In July 2011, the subject received 1st dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the first vaccination, the subject experienced injection site swelling, pyrexia, headache, and urticaria. The symptoms subsided in approximately 1 week, but headache and urticaria lasted 2 weeks. In October 2011, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). Within one month after 2nd dose of vaccine, the subject experienced the same symptoms as those after the first vaccination except urticaria. She also experienced malaise. One month after the second vaccination, the subject also experienced stomatitis, pyrexia, diarrhoea, abdominal pain, and dermatitis developed, and 2 months after vaccination, severe urticaria developed. In March 2012, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the third vaccination, the subject experienced arthralgia along with the same symptoms as those experienced after the second vaccination. Fourteen days after the vaccination, exertional dyspnoea and severe malaise were also developed. One month and a half after the vaccination, urticaria, pain in the lower and upper extremities, dermatitis, and stomatitis developed. Stomatitis, dermatitis, malaise, low back pain, slight fever, arthralgia, abdominal pain, and headache were developed and lasted for 2 or 3 months after vaccination. Hyperpnoea and a feeling of dyspnoea were also experienced even at rest as well as pedal oedema. Three to five months after the third vaccination, the subject experienced generalised joint pains, abdominal pain, headache, multiple stomatitis, inappetence, vomiting, slight fever, and parotitis. Six to nine months after the third vaccination, she experienced abnormal malaise, clouding of consciousness, anterior chest pain similar to angina pectoris and palpitations also developed. In addition, giddiness and excessive sleep were developed. The physician considered the events were clinically significant (or requiring intervention). Approximately 10 months after the third vaccination, the chest pain was resolved but replaced by hyperpnoea. Although the pain in the body improved, the subject still experienced fatigue, hypobulia, and reduced thinking. It was considered that the subject had depressive symptoms. The outcome of the rest of the events was unspecified.


Changed on 10/14/2018

VAERS ID: 497405 Before After
VAERS Form:1
Age:14.0
Sex:Female
Location:Foreign
Vaccinated:2011-07-01
Onset:0000-00-00
Submitted:2013-07-22
Entered:2013-07-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV2: HPV (CERVARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 UN / IM

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Arthralgia, Back pain, Chest pain, Depressed level of consciousness, Depression, Dermatitis, Diarrhoea, Dizziness, Dyspnoea exertional, Headache, Hypersomnia, Hyperventilation, Malaise, Mental impairment, Oedema peripheral, Pain in extremity, Palpitations, Parotitis, Pyrexia, Stomatitis, Urticaria, Vomiting, Abulia, Injection site swelling, Decreased appetite, Vaccine positive rechallenge

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: UNK
CDC 'Split Type': B0908384A

Write-up: This case was reported by a physician and described the occurrence of swelling injection site in a 14-year-old female subject who was vaccinated with CERVARIX (GlaxoSmithKline). In July 2011, the subject received 1st dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the first vaccination, the subject experienced injection site swelling, pyrexia, headache, and urticaria. The symptoms subsided in approximately 1 week, but headache and urticaria lasted 2 weeks. In October 2011, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). Within one month after 2nd dose of vaccine, the subject experienced the same symptoms as those after the first vaccination except urticaria. She also experienced malaise. One month after the second vaccination, the subject also experienced stomatitis, pyrexia, diarrhoea, abdominal pain, and dermatitis developed, and 2 months after vaccination, severe urticaria developed. In March 2012, the subject received 2nd dose of CERVARIX (intramuscular, unknown injection site and batch number). One week after the third vaccination, the subject experienced arthralgia along with the same symptoms as those experienced after the second vaccination. Fourteen days after the vaccination, exertional dyspnoea and severe malaise were also developed. One month and a half after the vaccination, urticaria, pain in the lower and upper extremities, dermatitis, and stomatitis developed. Stomatitis, dermatitis, malaise, low back pain, slight fever, arthralgia, abdominal pain, and headache were developed and lasted for 2 or 3 months after vaccination. Hyperpnoea and a feeling of dyspnoea were also experienced even at rest as well as pedal oedema. Three to five months after the third vaccination, the subject experienced generalised joint pains, abdominal pain, headache, multiple stomatitis, inappetence, vomiting, slight fever, and parotitis. Six to nine months after the third vaccination, she experienced abnormal malaise, clouding of consciousness, anterior chest pain similar to angina pectoris and palpitations also developed. In addition, giddiness and excessive sleep were developed. The physician considered the events were clinically significant (or requiring intervention). Approximately 10 months after the third vaccination, the chest pain was resolved but replaced by hyperpnoea. Although the pain in the body improved, the subject still experienced fatigue, hypobulia, and reduced thinking. It was considered that the subject had depressive symptoms. The outcome of the rest of the events was unspecified.

New Search

Link To This Search Result:

https://www.medalerts.org/vaersdb/findfield.php?IDNUMBER=497405&WAYBACKHISTORY=ON


Copyright © 2020 National Vaccine Information Center. All rights reserved.
21525 Ridgetop Circle, Suite 100, Sterling, VA 20166