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From the 1/14/2022 release of VAERS data:

Found 99,646 cases where Vaccine targets Shingles (VARZOS) and Submission Date on/before '2018-05-31'

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Case Details

This is page 6 out of 9,965

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VAERS ID: 264576 (history)  
Form: Version 1.0  
Age:   
Sex: Female  
Location: Maryland  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2006-10-10
Entered: 2006-10-16
   Days after submission:6
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. - / UNK UN / -

Administered by: Other       Purchased by: Other
Symptoms: Dermatitis bullous
SMQs:, Severe cutaneous adverse reactions (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (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: UNK
Current Illness:
Preexisting Conditions: UNK
Allergies:
Diagnostic Lab Data: UNK
CDC Split Type: WAES0609USA08568

Write-up: Information has been received from a physician concerning a female pt who was vaccinated with a dose of varicella zoster virus vaccine live. Subsequently the pt experienced a varicella like rash at the injection site. The phsyciain did not want to make a report because he felt it was part of the normal AE''s. No further information was available.


VAERS ID: 264577 (history)  
Form: Version 1.0  
Age: 64.0  
Sex: Female  
Location: Florida  
Vaccinated:2006-09-27
Onset:2006-09-27
   Days after vaccination:0
Submitted: 2006-10-10
   Days after onset:13
Entered: 2006-10-16
   Days after submission:6
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. 0621F / UNK UN / IM

Administered by: Other       Purchased by: Other
Symptoms: Pruritus
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), 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? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NONE
Current Illness:
Preexisting Conditions: NONE
Allergies:
Diagnostic Lab Data: NONE
CDC Split Type: WAES0610USA00311

Write-up: Information has been received from a 64 year old female with no allergies and an unremarkable medical history who on 9/27/06 was vaccinated IM with a 0.65 ml dose of varicella zoster virus vaccine live (lot 652925/0621F). There was no concomitant medication. On 9/27/06, one hour after vaccination, the pt experienced itching all over her body. The pt stated that she did not experience itching at the injection site. No medical attention was sought and no diagnostic lab tests were performed. At the time of the report, the pt was recovering. A product quality complaint was not involved. Additional information has been requested.


VAERS ID: 264578 (history)  
Form: Version 1.0  
Age: 60.0  
Sex: Male  
Location: California  
Vaccinated:2006-08-30
Onset:2006-09-01
   Days after vaccination:2
Submitted: 2006-10-10
   Days after onset:39
Entered: 2006-10-16
   Days after submission:6
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. 0622F / UNK UN / SC

Administered by: Other       Purchased by: Other
Symptoms: Injection site erythema, Injection site pain, Injection site rash
SMQs:, Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow)

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: UNK
Current Illness:
Preexisting Conditions: UNK
Allergies:
Diagnostic Lab Data: UNK
CDC Split Type: WAES0610USA00397

Write-up: Information has been received from a nurse practitioner regarding her husband who is over 60 years old who on 8/30/06 was vaccinated SC in the arm with a dose of varicella zoster virus vaccine live (lot 652965/0622F). Within a week after vaccination, in approx 9/06, pt developed about a 3cm circular area injection site rash on his arm that was red and sore for about a week after vaccination. Subsequently, the pt recovered. No medical attention was sought. A product quality complaint was not involved. Additional information has been requested. This is follow-up to report(s) previously submitted on 10/10/2006. Information has been received from a nurse practitioner regarding her husband who is "over 60 years old" and a physician who on 30-AUG-2006 was vaccinated SC (also reported as IM) in the deltoid with one dose of ZOSTAVAX (Merck) (Lot # 652965/0622F). Within a week after vaccination, in approximately September 2006, the patient developed about a 3 cm circular area injection site rash on his arm that was red and sore for about a week after vaccination. Subsequently, the patient recovered. No medical attention was sought. A product quality complaint was not involved. Additional information indicated that on 10-AUG-2006 the patient''s injection site was red. This lasted for one week and resolved on its own. No further information is available.


VAERS ID: 264579 (history)  
Form: Version 1.0  
Age:   
Sex: Female  
Location: California  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2006-10-10
Entered: 2006-10-16
   Days after submission:6
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Rash
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (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: UNK
Allergies:
Diagnostic Lab Data: NONE
CDC Split Type: WAES0610USA03496

Write-up: Information has been received from a physician concerning a female pt who was vaccinated with a dose of varicella zoster virus vaccine live. Subsequently the pt developed a rash of one pock on the opposite are she was injected in. Unspecified medical attention was sought. There was no product quality complaint involved. Additional information has been requested. This is in follow-up to report(s) previously submitted on 10/10/2006. Information has been received from a physician concerning a female patient who was vaccinated with a dose of ZOSTAVAX (Oka/Merck). There was no illness at the time of vaccination. Follow-up information indicated that the patient developed a mild case of shingles. There was no post-herpetic lesions as of yet and mild pain. The patient later stated that "maybe I didn''t have chickenpox". Although she said first that she did not have them. The patient recovered on an unspecified date. The patient had no adverse events following prior vaccination. Additional information is not expected.


VAERS ID: 264956 (history)  
Form: Version 1.0  
Age: 1.03  
Sex: Female  
Location: Utah  
Vaccinated:2006-10-17
Onset:0000-00-00
Submitted: 2006-10-18
Entered: 2006-10-19
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR U2174GA / 1 RL / IM
HEPA: HEP A (VAQTA) / MERCK & CO. INC. 0144F / 1 LL / IM
HIBV: HIB (PEDVAXHIB) / MERCK & CO. INC. 0494P / 3 LL / IM
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. 0981F / 1 LA / SC

Administered by: Public       Purchased by: Private
Symptoms: Medication error
SMQs:, Medication errors (narrow)

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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Zostavax given to 1 year old child rather than ProQuad. Parents advised to watch for redness, swelling at inj site, C Pox rash in 1-3 wks, bring child in for ProQuad in 3 months.


VAERS ID: 264957 (history)  
Form: Version 1.0  
Age: 5.0  
Sex: Female  
Location: Utah  
Vaccinated:2006-10-17
Onset:0000-00-00
Submitted: 2006-10-18
Entered: 2006-10-19
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTAP: DTAP (DAPTACEL) / SANOFI PASTEUR C2207AA / 4 LA / IM
IPV: POLIO VIRUS, INACT. (IPOL) / SANOFI PASTEUR Y1051 / 4 LA / SC
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. 0211F / 2 LA / SC
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. 0981F / 1 RA / SC

Administered by: Private       Purchased by: Public
Symptoms: Medication error
SMQs:, Medication errors (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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Zostavax given to 4 1/2 year old child rather than ProQuad. Parents advised to watch for redness, swelling at injection site, C pox rash in 1-3 weeks. Return child to clinic in 3 months for Varicella vaccine.


VAERS ID: 265040 (history)  
Form: Version 1.0  
Age: 74.0  
Sex: Male  
Location: Missouri  
Vaccinated:2006-10-11
Onset:2006-10-18
   Days after vaccination:7
Submitted: 2006-10-20
   Days after onset:2
Entered: 2006-10-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS 70089 / 1 RA / IM
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. 0981F / 1 LA / SC

Administered by: Unknown       Purchased by: Unknown
Symptoms: Anaemia, Dehydration, Hydronephrosis, Prostatic disorder, Pyrexia
SMQs:, Haematopoietic erythropenia (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (narrow)

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? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Meds: metamucil, Ergocalciferol, Flomax, Lidocaine/Prilocaine topical, Hyoscyamine sulfate PRN, vitamins, Vitamin D, and sulfamethoxazole-trimethoprim.
Current Illness: superficial wound infection with B. fragilis.
Preexisting Conditions: allergy-phenergan history of colectomy for ulcerative colitis, osteoporosis, vitamin D deficiency PMH: COPD, Hypertension, Hemorrhoids, Joint pain, Sleep Apnea, cataracts, osteoporosis, diverticuli, low back pain, anemia, sinusitis, allergic rhinitis and testosterone deficiency. Recent surgery for bowel obstruction with wound dehiscence.
Allergies:
Diagnostic Lab Data: CBC no shift, CXR, Urine culture, blood cultures negative. LABS and DIAGNOSTICS: Renal US shows mild left hydronephrosis and moderate postvoid residual.
CDC Split Type:

Write-up: Received Zostavax and flu vaccine on 10/11. Developed fever 102.4 documented on 10/18. Was admitted for IV fluids. No other obvious source found. Had recently been hospitalized and operated for small obstruction which made him susceptible to the dehydration factor. No infectious etiology found related to fever. Hospital and PCP MRs received documenting 73 yr old who presents 1 week s/p Flu and Zostavx immunizations with fever, dysuria, and not feeling well. Patient reports need to push on bladder to empty. Admitted to hospital for hydration and IV antibiotics. Impression: "Suspect UTI from inability to empty bladder well. Doubt reaction to Zostavax" Discharge DX: Fever, Dehydration, Hydronephrosis, BPH with outlet obstruction, concha bullosa, anemia, and past hx. of abd. incision dehiscence.


VAERS ID: 265199 (history)  
Form: Version 1.0  
Age: 76.0  
Sex: Female  
Location: Florida  
Vaccinated:2006-10-03
Onset:2006-10-04
   Days after vaccination:1
Submitted: 2006-10-23
   Days after onset:19
Entered: 2006-10-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Public       Purchased by: Unknown
Symptoms: Injection site pain
SMQs:, Extravasation events (injections, infusions and implants) (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: none noted.
Current Illness: none To prevent shingles which is not listed as a vaccine
Preexisting Conditions: none noted.
Allergies:
Diagnostic Lab Data: none
CDC Split Type:

Write-up: Pain and burning in muscle in shoulder area after receiving a shingles vaccine on Oct 3, 2006 and still hurting on Oct 23, 2006. Pt. reports that a vaccine for shingles was given NOT GARDASIL as reported. Pain and burning in shoulder began the next day and continued 3 weeks post vax. Still reporting that arm is sore but improving. Pt. also reports that beginning 10/19/2006 she began to experience swelling and itching around her Right eye with development of a blister, then scab near the right eye. She saw an eye doctor (OD) 10/23/06 who commented that it might be shingles. She then reported to him that she had the shingles vaccine 3 weeks prior. No other medical treatment sought. Office visit report received from eye OD which describes an ulcerated eyelid lesion above the right eye. Tx''d with Elestat PRN. Received Vax. record. Confirmed Zostavax (0981F) given on October 3,2006-not Gardasil as reported on VAERS form.


VAERS ID: 265213 (history)  
Form: Version 1.0  
Age: 45.0  
Sex: Female  
Location: Ohio  
Vaccinated:2006-07-01
Onset:2006-10-13
   Days after vaccination:104
Submitted: 2006-10-19
   Days after onset:6
Entered: 2006-10-24
   Days after submission:5
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. - / UNK UN / SC

Administered by: Other       Purchased by: Other
Symptoms: Herpes zoster, Pain, Viral infection
SMQs:, Opportunistic infections (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: UNK
Current Illness:
Preexisting Conditions: Shingles
Allergies:
Diagnostic Lab Data:
CDC Split Type: WAES0610USA10533

Write-up: Information has been received from a physician concerning a 45 year old female with a history of three shingles outbreaks (two in early 2006 and in in May 2006) and no allergies or other medical history who on 7/1/06 was vaccinated SC with a dose of varicella Zoster virus vaccine live. It was noted that a physician gave the vaccination to boost the pts immunity. On 10/13/06, the pt experienced a fourth outbreak of shingles. The pt experienced less pain and the outbreak was less severe than the first three outbreaks. She was treated with triamcinolone Acetonide (Kenalog) 1cc and Famciclovir (Famvir) 500 mg TID since 10/13/06. No diagnostic lab test were preformed. At the time of the report, the pts case of shingles was less severe and she was recovering. A product quality complaint was no involved. Shingles was considered to be an other important medical event by the reporter (OMIC). Additional information has been requested.


VAERS ID: 265225 (history)  
Form: Version 1.0  
Age: 65.0  
Sex: Female  
Location: Idaho  
Vaccinated:2006-10-09
Onset:2006-10-11
   Days after vaccination:2
Submitted: 2006-10-12
   Days after onset:1
Entered: 2006-10-24
   Days after submission:12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR U2240AA / UNK LA / IM
PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. 1047P / 1 LA / IM
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. 0621F / 1 LA / SC

Administered by: Public       Purchased by: Private
Symptoms: Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (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: Thyroid
Current Illness: NONE
Preexisting Conditions: NONE
Allergies:
Diagnostic Lab Data:
CDC Split Type: WA062153

Write-up: On Wed 10/11 had itching on left arm, beginning in the morning. on 10/12 had hive all over left arm on 10/13 noticed hives on right arm. Has not called MD has not taken any meds at time of report.


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