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Found 23,145 cases where Vaccine is MNQ

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VAERS ID: 242789 (history)  
Form: Version 1.0  
Age: 19.0  
Sex: Female  
Location: Massachusetts  
Vaccinated:2005-07-18
Onset:2005-07-20
   Days after vaccination:2
Submitted: 2005-06-29
   Days after onset:21
Entered: 2005-08-08
   Days after submission:40
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1684AA / 1 RA / IM

Administered by: Private       Purchased by: Unknown
Symptoms: Headache, Hypersensitivity, Rash
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), 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: Zyrtec
Current Illness:
Preexisting Conditions: seasonal allergies
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2005014000

Write-up: An initial report was received in the U.S.A. from a parent, who is employed by the health care provider on 07/20/2005. An 18 year old female patient developed headache and a rash on her lower back, under arms, back of knees and groin area two days after she had received an intra-muscular injection of Menactra in the right deltoid and an intra-dorsal injection of TUBERSOL in the left forearm. The rash was described as faint, pink small bumps. She does have a history of seasonal allergies for which she takes Zyrtec. She was treated with Motrin. It is unknown if she has recovered.


VAERS ID: 242792 (history)  
Form: Version 1.0  
Age: 17.0  
Sex: Male  
Location: California  
Vaccinated:2005-07-11
Onset:2005-07-15
   Days after vaccination:4
Submitted: 2005-07-27
   Days after onset:12
Entered: 2005-08-08
   Days after submission:12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1643AA / 1 LA / SC
TD: TD ADSORBED (TDVAX) / MASS. PUB HLTH BIOL LAB TD131 / UNK LA / IM

Administered by: Private       Purchased by: Unknown
Symptoms: Headache, Medication error, Nasal congestion, Pharyngolaryngeal pain, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Medication errors (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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: 200501379

Write-up: An initial report was received in the USA from a health care professional on 7/19/05. An 18 year old male patient experienced a fever of 103 degrees F, sore throat, nasal congestion and headache four days post vaccination after he had received a SC injection of Menactra, lot number U1641AA in the left arm and an IM injection of tetanus diphtheria, lot number TD131 in the left deltoid. The patient was prescribed Motrin and Tylenol and his fever was decreased to 101 degrees F. A CBC was done on 7/15/05 but results were not provided. The Menactra vaccine was administered incorrectly as SC instead of the IM route. It is unknown if the patient has recovered. Follow-up information received on 30-August-2005. This patient was 17 year old at the time of vaccination an the manufacturer for the tetanus diphtheria product is the Massachusetts Department of Health. The results of the CBC were provided - within normal limits. The patient did not have any significant medical history, was not on any medications and did not have any illness at the time of vaccination. The patient recovered from the adverse events.


VAERS ID: 242793 (history)  
Form: Version 1.0  
Age: 15.0  
Sex: Female  
Location: California  
Vaccinated:2005-06-10
Onset:2005-06-17
   Days after vaccination:7
Submitted: 2005-07-27
   Days after onset:40
Entered: 2005-08-08
   Days after submission:12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1641AA / 1 LA / SC

Administered by: Private       Purchased by: Unknown
Symptoms: Arthralgia, Headache, Medication error
SMQs:, Arthritis (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: MOTRIN
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: 200501382

Write-up: An initial report was received in the USA from a health care professional on 7/15/05. A 16 year old female patient complained of headache and joint pain of knees and elbows seven days after she had received SC injection of Menactra, lot number U1641AA, in the left arm. The vaccine was admnistered SC in stead of IM. She was treated with Motrin and her symptoms resolved. Follow-up information received on 30-August-2005. The patient received the vaccine on 10-June-2005 at 10:00 and the adverse events started 7 days later at 13:00. The patient also received MOTRIN concomitantly.


VAERS ID: 242794 (history)  
Form: Version 1.0  
Age: 11.0  
Sex: Male  
Location: California  
Vaccinated:2005-07-25
Onset:2005-07-26
   Days after vaccination:1
Submitted: 2005-07-29
   Days after onset:3
Entered: 2005-08-08
   Days after submission:10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1639AA / UNK LA / SC

Administered by: Private       Purchased by: Unknown
Symptoms: Injection site erythema, Injection site pain, Injection site warmth, 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? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Tubersol; Adderall
Current Illness:
Preexisting Conditions: Patient has a history of ADHD for which he takes Adderall. He had no illnesses at the time of vaccination.
Allergies:
Diagnostic Lab Data:
CDC Split Type: 200501444

Write-up: An initial report was received in the USA from a health care professional on 7/27/05. An 11 year old male patient complained of redness, pain and warmth at the left arm injection site one day after he had received a SC injection of Menactra, lot number U1639AA, instead of the IM route. He also received TUBERSOL in the left forearm. Treatment was not reported. Reportedly, he has not recovered.


VAERS ID: 242795 (history)  
Form: Version 1.0  
Age: 15.0  
Sex: Female  
Location: Ohio  
Vaccinated:2005-05-04
Onset:2005-06-12
   Days after vaccination:39
Submitted: 2005-07-19
   Days after onset:37
Entered: 2005-08-08
   Days after submission:20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR - / UNK - / IM
TDAP: TDAP (ADACEL) / SANOFI PASTEUR - / UNK - / IM

Administered by: Unknown       Purchased by: Unknown
Symptoms: Abortion
SMQs:, Termination of pregnancy and risk of abortion (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: Flonase
Current Illness:
Preexisting Conditions: The patient has a history of seasonal allergies and back pain for one year.
Allergies:
Diagnostic Lab Data: A home urine pregnancy test on 7/2/05 was reported as negative.
CDC Split Type: 200501115

Write-up: It was reported through a clinical trial in the USA that a 15 year old female subject was pregnant. Last menstrual period: 4/25/05, expected delivery date not provided. She has no previous obstetric history. Maternal drug exposure includes OrthoEvra Patch (5/8/05 - 5/30/05), Tylenol (5/6/05), Flonase (Mid March 2005 - present), Diazepam (6/1/05), Tylenol Arthritis(date not provided, Cyclobenzaprine HCl (6/1/05) and Flurbiprofen (5/31/05). The subject received her first dose of the study vaccine on 5/4/05, she did not experience any adverse event. The Adacel IND number 9266, has been added to this case. From additional information received on 7/8/05, it was reported that the subject had an elective abortion performed on 6/12/05. A home urine pregnancy test on 7/2/05 was reported as negative.


VAERS ID: 242478 (history)  
Form: Version 1.0  
Age: 13.0  
Sex: Female  
Location: Unknown  
Vaccinated:2005-06-20
Onset:2005-06-30
   Days after vaccination:10
Submitted: 2005-07-05
   Days after onset:5
Entered: 2005-08-09
   Days after submission:35
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1526AC / UNK - / IM

Administered by: Private       Purchased by: Private
Symptoms: Decreased appetite, Headache, Photophobia, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious meningitis (narrow), Glaucoma (broad), Corneal disorders (broad), Retinal disorders (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? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NONE
Current Illness: NONE
Preexisting Conditions: NONE
Allergies:
Diagnostic Lab Data:
CDC Split Type: AK200555

Write-up: Meningeal symptoms - headache, fever (100.8), photophobia, decreased appetite.


VAERS ID: 242661 (history)  
Form: Version 1.0  
Age: 18.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2005-07-01
Onset:0000-00-00
Submitted: 2005-08-08
Entered: 2005-08-10
   Days after submission:2
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR - / UNK - / -

Administered by: Unknown       Purchased by: Unknown
Symptoms: Arthralgia, Condition aggravated, Convulsion, Diarrhoea, Fatigue, Headache, Nausea, Pyrexia, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Convulsions (narrow), Pseudomembranous colitis (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Generalised convulsive seizures following immunisation (narrow), Arthritis (broad), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (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:
Current Illness:
Preexisting Conditions: The patient has a past medical history of epilepsy, which was diagnosed five years ago.
Allergies:
Diagnostic Lab Data: UNK
CDC Split Type: 200501500

Write-up: Initial report received from the patient on 8/4/05. It was reported that the 18 year old female patient, who had a past history of epilepsy, had received a dose of Menactra, lot number not reported, in July 2005. The route and site of administration were not reported. An unspecified amount of time later, the patient experienced seizures, nausea, vomiting, diarrhea, headache, achy joints, fever, and fatigue. it is unknown whether the patient required any medical intervention. Her recovery status is listed as unknown. (OMIC)


VAERS ID: 242662 (history)  
Form: Version 1.0  
Age: 15.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2005-07-25
Onset:2005-07-27
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2005-08-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1492AB / 1 - / IM

Administered by: Private       Purchased by: Private
Symptoms: Laboratory test abnormal, Leukopenia, Monocytosis, Neutropenia, Platelet disorder, Pyrexia, Thrombocytopenia, White blood cell disorder
SMQs:, Agranulocytosis (broad), Haematopoietic leukopenia (narrow), Haematopoietic thrombocytopenia (narrow), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic 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? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: The pt has no known allergies or medical conditions. She had no illnesses at the time of vaccination.
Allergies:
Diagnostic Lab Data: 29Jul05: WBC 2.4x10^3/uL (4.0-12.5); Platelets 75x10^3/uL (140-440); Neutrophils 32% (38-63); Lymphs 53% (27-47; Monocytes 14% (4-13); Neutrophils 0.8 x10^3/uL (1.5-7.8); Lymphs 1.3x10^3/uL (1.1-5.9); Monocytes 0.3x10^3/uL (0.2-1.6). The pt is currently being tested for Epstein Barr, but the results were not reported.
CDC Split Type: 200501513

Write-up: Initial information received on 8/5/05 and 8/8/05. A 15 year old female patient had received an IM injection of Menactra, lot number U1492AB, on 7/25/05. Two days later, the patient developed a fever. Three days later, her blood work displayed leukopenia, neutropenia, and thrombocytopenia. The patient was seen by a physician and is currently being tested for Epstein Barr virus. At the time of this report she had not recovered from these events. (OMIC)


VAERS ID: 242667 (history)  
Form: Version 1.0  
Age: 12.0  
Sex: Male  
Location: Nebraska  
Vaccinated:2005-07-29
Onset:2005-07-29
   Days after vaccination:0
Submitted: 2005-08-01
   Days after onset:3
Entered: 2005-08-10
   Days after submission:9
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1659AA / 1 LA / IM
UNK: VACCINE NOT SPECIFIED (NO BRAND NAME) / UNKNOWN MANUFACTURER U1565BA / 7+ RA / IM

Administered by: Private       Purchased by: Private
Symptoms: Asthenia, Dizziness, Feeling hot, Injection site erythema, Oedema, Pain, Pallor, Pruritus
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (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? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zyrtec, Rhinocort
Current Illness: NONE
Preexisting Conditions: Allergic rhinitis
Allergies:
Diagnostic Lab Data: NONE
CDC Split Type:

Write-up: Shortly after vaccine received, left arm itching (severe), swelling, redness, pain c/o dizziness, hot to touch, pale, weak, no SOB or wheezing. Rec ER visit, mom refused. Pain sensation, radiation into shoulder and neck.


VAERS ID: 242668 (history)  
Form: Version 1.0  
Age: 15.0  
Sex: Male  
Location: Florida  
Vaccinated:2005-07-26
Onset:2005-07-27
   Days after vaccination:1
Submitted: 2005-07-29
   Days after onset:2
Entered: 2005-08-10
   Days after submission:12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1677AA / 1 - / IM

Administered by: Private       Purchased by: Private
Symptoms: Eczema
SMQs:, 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: NONE
Current Illness: NONE
Preexisting Conditions: Eczema
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Eczema flair, face, 2.5% hytone lotion, Cetaphil.


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