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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 4 out of 9,965

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VAERS ID: 264024 (history)  
Form: Version 1.0  
Age:   
Sex: Male  
Location: New York  
Vaccinated:2006-09-08
Onset:2006-09-09
   Days after vaccination:1
Submitted: 2006-10-02
   Days after onset:23
Entered: 2006-10-05
   Days after submission:3
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. - / UNK UN / -

Administered by: Other       Purchased by: Other
Symptoms: Herpes zoster, Rash
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Opportunistic infections (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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: UNK
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: WAES0609USA06560

Write-up: Information has been received from a physician concerning a male pt who on 9/9/06 was vaccianted with a dose of varicella zoster virus vaccine live. On 9/8/06 the pt was hospitalized with a rash. The was diagnosed with a zoster infection. No outcome was reported. No product quality complaint was involved. Additional information has been requested.


VAERS ID: 264187 (history)  
Form: Version 1.0  
Age: 80.0  
Sex: Female  
Location: California  
Vaccinated:2006-09-15
Onset:0000-00-00
Submitted: 2006-10-04
Entered: 2006-10-10
   Days after submission:6
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. 0622F / UNK UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Herpes zoster
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:
Allergies:
Diagnostic Lab Data:
CDC Split Type: WAES0610USA00298

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 shingles. Unspecified medical attention was sought. The pt was administered acyclovir for the shingles. A product quality complaint was not involved. Shingles was considered to be an other important medical event by the reporter (OMIC). Additional information has been requested.


VAERS ID: 264210 (history)  
Form: Version 1.0  
Age: 63.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2006-09-28
Onset:2006-10-01
   Days after vaccination:3
Submitted: 2006-10-02
   Days after onset:1
Entered: 2006-10-10
   Days after submission:8
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. 0981F / 2 RA / -

Administered by: Private       Purchased by: Private
Symptoms: Injection site erythema, Injection site warmth, Liver disorder, Skin ulcer
SMQs:, Hepatic failure, fibrosis and cirrhosis and other liver damage-related conditions (narrow), Extravasation events (injections, infusions and implants) (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:
Current Illness: NONE
Preexisting Conditions: NONE
Allergies:
Diagnostic Lab Data: Diffuse hepatic like lesions
CDC Split Type:

Write-up: 63 year old female non immunocompromised received Zostavax Immunization on 9/28/06, on 10/01/06 developed diffuse hepatic lesions on body. Mild erythema and warm over injection site.


VAERS ID: 264422 (history)  
Form: Version 1.0  
Age: 70.0  
Sex: Male  
Location: Unknown  
Vaccinated:2006-07-03
Onset:2006-07-12
   Days after vaccination:9
Submitted: 2006-10-06
   Days after onset:86
Entered: 2006-10-12
   Days after submission:6
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. - / UNK UN / SC

Administered by: Other       Purchased by: Other
Symptoms: Hypoacusis, Loss of consciousness, Vertigo, Vomiting
SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hearing impairment (narrow), Vestibular disorders (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: WAES0609USA06711

Write-up: Information has been received from an investigator concerning a 70 year old male who entered a study, title as stated above. On 7/3/06 the pt was vaccinated SC in the deltoid region of the arm with a .065 ml dose of Varicella Zoster virus vaccine live. On approx 7/10/06, one week after vaccination, the pt was vaccinated with travel immunizations which included Hep A, typhoid vaccine and DPT. It was reported that the pt has been instructed not to receive any other vaccinations within one month of receiving varicella zoster virus vaccine live. About 48 hours after receiving the travel immunization, on 7/12/06, the pt developed vomiting, vertigo and passed out while at home. The vertigo was severe enough of the pt, who is a dentist, to cancel his appointments. The pt reported that he went to his primary physician on 7/17/06 and was determined to have hearing loss. The reporting investigator felt that hearing loss, vomiting and vertigo were possibly related to vaccination with varicella zoster virus vaccine live. Hearing loss, vomiting and vertigo were considered to be other important medical events (OMIC). Additional information has been requested.


VAERS ID: 264461 (history)  
Form: Version 1.0  
Age: 87.0  
Sex: Female  
Location: Indiana  
Vaccinated:2006-09-14
Onset:0000-00-00
Submitted: 2006-10-09
Entered: 2006-10-13
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. 0621F / UNK UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Hyperventilation, Tremor
SMQs:, Anaphylactic reaction (broad), Asthma/bronchospasm (broad), Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Eosinophilic pneumonia (broad), Hypoglycaemia (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: CONCURRENT CONDITIONS: Alzheimer''s disease
Allergies:
Diagnostic Lab Data:
CDC Split Type: WAES0609USA07481

Write-up: Information has been received from a physician concerning a 70 year old female with Alzheimer''s disease who on in September 2006 was vaccinated with a dose of varicella zoster vaccine live. The patient experienced tremors and hyperventilated when receiving the vaccine and the patient was taken to the emergency room. Subsequently the patient recovered. The physician believed that "the experience was more anxiety related than a reaction to the vaccine. There was no product quality complaint involved. The patient''s experiences were considered to be an important medical events. Additional information has been requested. (OMIC)


VAERS ID: 264559 (history)  
Form: Version 1.0  
Age: 41.0  
Sex: Female  
Location: New York  
Vaccinated:2006-09-05
Onset:2006-09-05
   Days after vaccination:0
Submitted: 2006-10-10
   Days after onset:35
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: Eye irritation, Medication error, Ocular hyperaemia
SMQs:, Anaphylactic reaction (broad), Glaucoma (broad), Corneal disorders (broad), Medication errors (narrow)

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: UNK
Allergies:
Diagnostic Lab Data: NONE
CDC Split Type: WAES0609USA00659

Write-up: Information has been received from a 41 year old female registered nurse who on 9/5/06 was sprayed in the eyes with varicella zoster virus vaccine live (lot 0495F). She reported that the syringe and the needle separated after the Diluent had been added to the vaccine and the vaccine sprayed out the needle and got in her eyes. Her eyes were washed out. The nurse reported that her eyes were red and irritated and she had an appointment to see an ophthalmologist. No lab studies were performed. There was no product quality complaint involved.


VAERS ID: 264562 (history)  
Form: Version 1.0  
Age: 53.0  
Sex: Female  
Location: Unknown  
Vaccinated:2006-08-30
Onset:2006-09-02
   Days after vaccination:3
Submitted: 2006-10-10
   Days after onset:38
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: Herpes zoster, Pruritus, Viral infection
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Opportunistic infections (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: Premarin
Current Illness:
Preexisting Conditions: Neuroma, Blind right eye, deafness right ear, chickenpox, allergic reaction to antibiotics, drug hypersensitivity.
Allergies:
Diagnostic Lab Data: NONE
CDC Split Type: WAES0609USA02489

Write-up: Information has been received from a pharmacist concerning a 53 year old female with allergies to erythromycin, tetracycline. Cephalexin (Keflex) and preservatives in eye ointments and a history of acoustic neuromomas of the brain with blindness in the right eye and deafness in the right ear who on 8/30/06 was vaccinated SC with a 0.65 ml dose of varicella zoster virus vaccine live (lot 652965/0622F). Concomitant therapy included estrogens, conjugated (Premarin). ON 9/2/06 the pt developed shingles on her arm and itching. No pain was noted. Unspecified medical attention was sought and the pt was treated with Valtrex. No lesions were remaining for VZV analysis. The pt had no history of shingles in the past, but a history of chickenpox as a child. Subsequently, the pt recovered from shingles. There was no product quality complaint involved. Additional information has been requested.


VAERS ID: 264563 (history)  
Form: Version 1.0  
Age:   
Sex: Female  
Location: Ohio  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2007-03-23
Entered: 2006-10-16
   Days after submission:158
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. - / UNK UN / SC

Administered by: Other       Purchased by: Other
Symptoms: Injection site rash, Injection site vesicles
SMQs:, 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: NONE
CDC Split Type: WAES0609USA03164

Write-up: Information has been received from a physician concerning a female pt who was vaccinated SC with a dose of varicella zoster virus vaccine live. Subsequently a few days after vaccination, the pt developed a linear blister at injection site. It was reported that the pt improved on an unspecified therapy and the pt recovered within a day. Medical attention was not 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 SC with a dose of ZOSTAVAX (Merck). Subsequently a few days after vaccination, the patient developed a linear blister at injection site. It was reported that the patient improved on an unspecified therapy and the patient recovered within a day. Medical attention was not sought. There was no product quality complaint involved. Additional information has been received from the physician''s office which indicated that the patient had a light rash at the injection site for 24 hours. There were no other problems and no work up. No further information is expected.


VAERS ID: 264564 (history)  
Form: Version 1.0  
Age: 66.0  
Sex: Female  
Location: D.C.  
Vaccinated:2006-09-11
Onset:2006-09-11
   Days after vaccination:0
Submitted: 2006-10-10
   Days after onset:29
Entered: 2006-10-16
   Days after submission:6
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. 0622F / 1 UN / SC

Administered by: Private       Purchased by: Private
Symptoms: Herpes zoster, Injection site rash, Rash, Viral infection
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), 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: NONE
Current Illness:
Preexisting Conditions: Chickenpox;
Allergies:
Diagnostic Lab Data: UNKNOWN
CDC Split Type: WAES0609USA03622

Write-up: Information has been received from a registered nurse concerning a 66 year old female with no known medical history or allergies who on 9/11/06 was vaccinated SC with a 0.5ml dose of varicella zoster virus live (lot 652965/0622F. It was reported that the pt was vaccinated because she had a strong family history of shingles. There was no concomitant medication. On 9/13/06 the pt developed a rash at the injection site and on other body areas. She went to the ER to be treated and was place on Valtrex. Additional information from the registered nurse indicated that the pt told the ER that she had shingles and that her shingles might get worse. She was given a prescription, but the pt didn''t know if she was going to take it. She thought she would try BeBaum for the rash instead. The pt cancelled her appointment for follow up. The nurse reported that the pt had a minor case and was walking and talking fine. At the time of the report, the pt was recovering. Additional information has been requested. It was reported that the patient had a chickenpox as a child. There was no recent exposure to chickenpox or herpes zoster noted. Additional information indicated on 09/14/06 (also reported as 09/13/06) in the evening the patient developed a rash, went to the ER and was diagnosed with shingles treated with valacyclovir hydrochloride (VALTREX). The nurse reported the patient had a follow-up appointment and was a "no-show". Multiple phone attempts were made and the nurse was unable to reach the patient, therefore no resolution was obtained. No further information is expected.


VAERS ID: 264565 (history)  
Form: Version 1.0  
Age: 64.0  
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 / SC

Administered by: Other       Purchased by: Other
Symptoms: Injection site oedema, Injection site rash
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow)

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: UNK
Current Illness:
Preexisting Conditions: UNK
Allergies:
Diagnostic Lab Data: UNK
CDC Split Type: WAES0609USA03864

Write-up: Information has been received from a medical assistant concerning a 64 year old female who on an unspecified date was vaccinated SC with a 0.5 ml dose of varicella zoster virus vaccine live. Subsequently, the pt experienced an injection site rash measuring 7x3.5 cm and injection site swelling. Unspecified medical attention was sought. Subsequently, the pt recovered a week after vaccination. No product quality complaint was involved. Additional information has been requested.


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