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Found 23,365 cases where Vaccine is MNQ

Case Details

This is page 11 out of 2,337

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VAERS ID: 241049 (history)  
Form: Version 1.0  
Age: 16.0  
Sex: Female  
Location: Michigan  
Vaccinated:2005-07-05
Onset:2005-07-06
   Days after vaccination:1
Submitted: 2005-07-06
   Days after onset:0
Entered: 2005-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1658AA / 1 LA / IM

Administered by: Unknown       Purchased by: Unknown
Symptoms: Asthenia, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (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: No illness or any recent illness
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Fever of 102.7 degrees orally on A.M. of 7/6/2005. Pt also feels weak.


VAERS ID: 241066 (history)  
Form: Version 1.0  
Age: 9.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2005-06-29
Onset:2005-06-30
   Days after vaccination:1
Submitted: 2005-07-06
   Days after onset:6
Entered: 2005-07-07
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR UE289AA / 1 LA / SC
TYP: TYPHOID LIVE ORAL TY21A (VIVOTIF) / BERNA BIOTECH, LTD. 3000808 / 1 MO / PO

Administered by: Private       Purchased by: Private
Symptoms: Abdominal pain
SMQs:, Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (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: NONE
Current Illness: NONE
Preexisting Conditions: NKA
Allergies:
Diagnostic Lab Data: NONE
CDC Split Type:

Write-up: 7/5/05 Received message from parent, patient experiencing abdominal cramping. Taken dose 1 and 2. Parent stopping 3 and 4. Started morning after dose 1.


VAERS ID: 241085 (history)  
Form: Version 1.0  
Age: 18.0  
Sex: Female  
Location: California  
Vaccinated:2005-05-25
Onset:2005-05-27
   Days after vaccination:2
Submitted: 2005-06-09
   Days after onset:13
Entered: 2005-07-08
   Days after submission:29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1588AA / UNK UN / IM

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: Claritin
Current Illness:
Preexisting Conditions: The pt has a history of eczema.
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2005010690

Write-up: From initial info received on 6/3/05 from a physician regarding an adverse event occurring in the USA, it was reported that an 18 year old female pt received a dose of Menactra, lot U1588AA, IM in an unspecified site on 5/25/05. Two days later, on 5/27/05, the pt developed a rash on her face and neck. The pt was seen by a physician. Per the reporter, the pt recovered from the event.


VAERS ID: 241086 (history)  
Form: Version 1.0  
Age: 58.0  
Sex: Male  
Location: D.C.  
Vaccinated:2005-06-02
Onset:2005-06-03
   Days after vaccination:1
Submitted: 2005-06-27
   Days after onset:24
Entered: 2005-07-08
   Days after submission:11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS AHAVB043BA / UNK - / -
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1492 / 1 - / -

Administered by: Private       Purchased by: Private
Symptoms: Flushing, Medication error
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), 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: Celebrex, Flexeril, Prilosec
Current Illness:
Preexisting Conditions: The pt has an allergy to Ceftin derivatives. He had no illnesses at the time of vaccination.
Allergies:
Diagnostic Lab Data:
CDC Split Type: 200501081

Write-up: From initial info received on 6/7/05 from a health care professional regarding an adverse event occurring in the USA, it was reported that a 58 year old male pt received a dose of Menactra, lot U1492AB and a dose of Havrix, lot AHAVB0543BA, administered on 6/2/05. The routes and sites of administration were unknown as per the reporter. The following day, on 6/3/05, the pt developed redness on his face, entire arms and legs. There was no itching and no fever reported. The duration of the redness was 2 days and the symptoms then disappeared. The pt recovered from the event. Follow up report received on Sept 6, 2005 from a health care professional. It is reported that no previous doses of Havrix was given prior to the June 2m, 2005 injection. No laboratory testing was done. Information was reviewed by the responsible physician and no addiitonal information can be provided at this time. No further information is expected.


VAERS ID: 241087 (history)  
Form: Version 1.0  
Age: 16.0  
Sex: Male  
Location: Texas  
Vaccinated:2005-06-06
Onset:2005-06-07
   Days after vaccination:1
Submitted: 2005-06-15
   Days after onset:8
Entered: 2005-07-08
   Days after submission:23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEPA: HEP A (VAQTA) / MERCK & CO. INC. AHAVB010AB / 2 LA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1573AC / 1 RA / IM

Administered by: Private       Purchased by: Private
Symptoms: Chest X-ray normal, Erythema, Full blood count normal, Lymph node pain, Lymphadenopathy, Lymphoedema, Myalgia, Red blood cell sedimentation rate increased, Ultrasound scan abnormal
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Retroperitoneal fibrosis (broad), Malignancy related therapeutic and diagnostic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), 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:
Current Illness: NONE
Preexisting Conditions: The patient denied any significant past medical history or illnesses at the time of vaccination.
Allergies:
Diagnostic Lab Data: CXR negative; Sono of chest-worse-lymphedema only; CBC nl; ESR=18mm/hr
CDC Split Type: 200501114

Write-up: From initial info received on 6/9/05 from an RN regarding an adverse occurring in the USA, it was reported that a 16 year old male pt received his 1st dose of Menactra, lot U1573AC, IM, RA, as well as his 2nd dose of Hep-A, lot AHAVB010AB, IM, LA on 6/6/05. The following day, on 6/7/05, the pt developed an enlarged lymph node with profuse redness and tenderness in the axillary area, which spread across his latissimus dorsal muscle and extended to the chest and nipple area. The pt was seen by a physician. It was not reported whether the pt recovered from these events.


VAERS ID: 241088 (history)  
Form: Version 1.0  
Age: 12.0  
Sex: Male  
Location: South Carolina  
Vaccinated:2005-06-13
Onset:2005-06-15
   Days after vaccination:2
Submitted: 2005-06-28
   Days after onset:13
Entered: 2005-07-08
   Days after submission:10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1640AA / 1 LA / -

Administered by: Private       Purchased by: Other
Symptoms: Rash, 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? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Albuterol
Current Illness:
Preexisting Conditions: The pt has a past medical history of asthma and is allergic to Cefadyl. The pt had no illnesses at the time of vaccination.
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2005011830

Write-up: From initial info received on 6/17/05 from an RN regarding an adverse event occurring in the USA, it was reported that an 11 year old male pt received his 1st dose of Menactra vaccine, lot U1640AA, administered in the left deltoid on 6/13/05. Reportedly, 2 days later, on 6/15/05, the pt developed a rash on his face and hands. Two days later, on 6/17/05, the rash progressed to welts on his torso. He had no complaints of fever or itching. The symptoms were treated with Benadryl. The pt''s recovery status was reported as not recovered.


VAERS ID: 241089 (history)  
Form: Version 1.0  
Age: 18.0  
Sex: Male  
Location: Texas  
Vaccinated:2005-06-17
Onset:2005-06-28
   Days after vaccination:11
Submitted: 0000-00-00
Entered: 2005-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEPA: HEP A (VAQTA) / MERCK & CO. INC. M1090D / 1 LA / -
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1659AA / 1 RA / IM

Administered by: Other       Purchased by: Other
Symptoms: Purpura
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), 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: Tubersol 5 TU, lot C207AA, ID, left forearm
Current Illness:
Preexisting Conditions: The pt has no significant past medical history and did not have any significant illnesses at the time of vaccination.
Allergies:
Diagnostic Lab Data: Laboratory data obtained included a urinalysis, CBC, BUN, creatine and electrolytes. No results were provided at this time.
CDC Split Type: 2005012500

Write-up: From initial info received on 6/28/05 from a physician regarding an adverse event occurring in the USA, it was reported that an 18 year old male pt received his 1st dose of Menactra, lot U1659AA, administered IM in the right deltoid, a dose of Tubersol 5 TU, lot C207AA, administered ID in the left forearm and a dose of hepatitis A vaccine, lot M1090D, administered in the left deltoid on 6/17/05. Eleven days later, on the morning of 6/28/05, the pt developed generalized purpura. The pt was seen by a physician. It is unknown at this time whether the pt recovered from this event.


VAERS ID: 241090 (history)  
Form: Version 1.0  
Age: 17.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2005-06-29
Onset:2005-06-29
   Days after vaccination:0
Submitted: 2005-07-01
   Days after onset:2
Entered: 2005-07-08
   Days after submission:7
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1657AA / UNK LA / IM

Administered by: Other       Purchased by: Other
Symptoms: Rash macular
SMQs:, 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:
Current Illness:
Preexisting Conditions: The pt''s past medical history is significant for anaphylaxis following an insect bite and she carries an EpiPen. The pt had no illnesses at the time of vaccination.
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2005012530

Write-up: From initial info received on 6/29/05 from a physician, regarding an adverse event occurring in the USA, it was reported that a 17 year old female pt received a dose of Menactra, lot U1657AA, IM in the left arm at 14:00 on 6/29/05. 90 minutes post vaccination, the pt developed red, blotchy patches over her elbows and knees. She was seen by a physician and treated with Benadryl 50mg per os. The pt recovered from this event.


VAERS ID: 241092 (history)  
Form: Version 1.0  
Age: 19.0  
Sex: Female  
Location: Florida  
Vaccinated:2005-06-01
Onset:2005-06-02
   Days after vaccination:1
Submitted: 2005-06-09
   Days after onset:7
Entered: 2005-07-08
   Days after submission:29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1525AB / 1 LA / SC

Administered by: Private       Purchased by: Other
Symptoms: Injection site erythema, Injection site pain, Injection site swelling, Medication error
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), 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: Humalog, vasotec
Current Illness:
Preexisting Conditions: The pt has a past medical history of diabetes.
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2005010520

Write-up: From initial info received on 6/3/05 from a health care professional regarding an adverse event occurring in the USA, it was reported that an 18 year old female pt received her 1st dose of Menactra vaccine on 6/1/05. The product was administered SC in error, in the back of the pt''s left arm. The next day, on 6/2/05, the pt developed a local reaction of redness, swelling and soreness at the site of injection. She was evaluated by a physician on 6/3/05. The pt was treated with ibuprofen and it is unknown whether she recovered from the events.


VAERS ID: 241093 (history)  
Form: Version 1.0  
Age:   
Sex: Female  
Location: South Carolina  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2005-06-28
Entered: 2005-07-08
   Days after submission:10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1575AA / 1 LA / SC

Administered by: Private       Purchased by: Private
Symptoms: Injection site erythema, Medication error
SMQs:, Extravasation events (injections, infusions and implants) (broad), 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: The pt did not have any pre-existing allergies or medical conditions. There is no illnesses or medications at the time of vaccination.
Allergies:
Diagnostic Lab Data: No lab test performed.
CDC Split Type: 2005011440

Write-up: From initial info received on 6/13/05 from a health care professional regarding an adverse event occurring in the USA, it was reported that a female pt received a dose of Menactra vaccine, lot U1575AA, SC instead of IM, in the left upper arm on an unspecified date. An unspecified amount of time later, the pt developed large redness of her left upper arm. At the time of this report, the pt recovered from these events.


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