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From the 10/15/2021 release of VAERS data:

Found 10,258 cases where Vaccine is MENB



Case Details

This is page 39 out of 1,026

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VAERS ID: 625897 (history)  
Form: Version 1.0  
Age: 16.0  
Sex: Female  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2016-02-18
Entered: 2016-02-26
   Days after submission:8
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MENB: MENINGOCOCCAL B (TRUMENBA) / PFIZER/WYETH - / UNK AR / IM

Administered by: Other       Purchased by: Other
Symptoms: Headache, Immediate post-injection reaction
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: No other medications
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2015389561

Write-up: This is a spontaneous report from a contactable nurse through a Pfizer representative. A 16 years old female patient received TRUMENBA on an unknown date, at 0.5 ml single, intramuscular, in arm. Medical history and concomitant medications were not reported. The patient experienced headache on an unknown date immediately after receiving the vaccine. The event resolved on an unknown date. Follow-up (17DEC2015): Follow-up attempts are completed. No further information is expected.


VAERS ID: 625899 (history)  
Form: Version 1.0  
Age: 16.0  
Sex: Female  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2016-02-18
Entered: 2016-02-26
   Days after submission:8
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK UN / UN
MENB: MENINGOCOCCAL B (TRUMENBA) / PFIZER/WYETH - / UNK UN / UN
MNQ: MENINGOCOCCAL CONJUGATE (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Headache
SMQs:

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: No other medications
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2015387109

Write-up: This is a spontaneous report obtained from a contactable nurse through a Pfizer sales representative. A 16-year-old female patient of an unspecified ethnicity received a single dose of TRUMENBA, a single dose of MCV4 (manufacturer unknown) and a single dose of quadrivalent flu vaccine, all on an unspecified date. Medical history and concomitant medications were not reported. On an unspecified date, the patient experienced a bad headache. Clinical outcome of the event was unknown at time of this report. Follow-up (19DEC2015): Follow-up attempts are completed. No further information is expected.


VAERS ID: 625900 (history)  
Form: Version 1.0  
Age: 18.0  
Sex: Male  
Location: California  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2016-02-18
Entered: 2016-02-26
   Days after submission:8
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MENB: MENINGOCOCCAL B (TRUMENBA) / PFIZER/WYETH - / UNK UN / IM

Administered by: Other       Purchased by: Other
Symptoms: Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (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: No other medications
Current Illness: Unknown
Preexisting Conditions: Human papilloma vaccine, Syncope
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2015377806

Write-up: This is a spontaneous report from a contactable consumer via a Pfizer sales representative. A 18-years-old male patient of an unspecified ethnicity received TRUMENBA, intramuscular on an unspecified date at 0.5 ml, single dose. The patient medical history was none, the patient was healthy and the patient''s did not receive any concomitant medications. The patient previously took human papilloma vaccine and experienced syncope. The patient experienced fainted on an unspecified date with outcome of unknown. Follow-up (15JAN2016): Follow-up attempts completed. No further information expected.


VAERS ID: 625902 (history)  
Form: Version 1.0  
Age: 20.0  
Sex: Female  
Location: Unknown  
Vaccinated:2015-10-12
Onset:2015-10-12
   Days after vaccination:0
Submitted: 2016-02-18
   Days after onset:129
Entered: 2016-02-26
   Days after submission:8
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MENB: MENINGOCOCCAL B (TRUMENBA) / PFIZER/WYETH J28923 / 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? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: No other medications
Current Illness: Unknown
Preexisting Conditions: Asthma
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2015371795

Write-up: This is a spontaneous report from a contactable physician reported through a Pfizer sales representative. A 20-years-old female patient received TRUMENBA (Lot number J28923, exp. date Jun2016, NDC number of TRUMENBA: 0005-0100-05), via an unspecified route of administration on 12Oct2015 at 0.5ml single dose. Medical history included asthma diagnosed when the patient was little. The patient''s concomitant medications were not reported. On the same date the patient experienced rash near where injection site would have been. The patient was treated with BENADRYL. The outcome was unknown. Follow-up (09DEC2015): Follow-up attempts are completed. No further information is expected.


VAERS ID: 625908 (history)  
Form: Version 1.0  
Age: 18.0  
Sex: Female  
Location: Florida  
Vaccinated:2016-01-06
Onset:2016-01-07
   Days after vaccination:1
Submitted: 2016-02-22
   Days after onset:46
Entered: 2016-02-26
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MENB: MENINGOCOCCAL B (TRUMENBA) / PFIZER/WYETH M13066 / UNK LA / IM

Administered by: Private       Purchased by: Private
Symptoms: Arthralgia, Asthenia, Fatigue, Headache, Injection site pain, Nausea, Pain
SMQs:, Acute pancreatitis (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Arthritis (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: No other medications
Current Illness: None
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2016008373

Write-up: This is a spontaneous report from a contactable consumer and subsequently from a contactable nurse on behalf of physician. A 18-year-old female patient received TRUMENBA (Lot # M13066, Expiration Date 30Sep2016) intramuscular 0.5 ml single dose in the left arm on 06Jan2016 15:30. Medical history and concomitant medications were not reported. The patient complained of weak on 07Jan2016 with outcome of recovered, terrible headache on Jan2016 with outcome of recovering, fatigue on 07Jan2016 with outcome of recovered, joint pain in knees on 07Jan2016 with outcome of recovered, really sore in vaccine area on 07Jan2016 with outcome of recovered, a little nausea on 06Jan2016 with outcome of recovered, pain on 06Jan2016 with outcome of recovered. Clinical course was reported as follows: The patient received TRUMENBA on 06Jan2016 and during the night she woke up with a little nausea and some pain. By the time she woke up on 07Jan2016 morning and the nausea was gone, but the pain had worsened, she had a terrible headache, was weak, had fatigue, joint pain in her knees and was really sore where the vaccine had been administered. The adverse events did not require an emergency room or doctor visit. She took ADVIL on 07Jan2016 night and her mom was a pediatrician who monitored her. The nurse was provided with the information regarding the adverse events by the patient. The nurse considered there was a reasonable possibility that the event is related to suspect product. The nurse was willing to be contacted again by Pfizer on the reported adverse events. Follow up (17Feb2016): New information reported from a contactable nurse on behalf of physician included: suspect dosage; indication detail; reported informed regarding the adverse events; reporter event causality assessment; reporter further contactability.


VAERS ID: 625909 (history)  
Form: Version 1.0  
Age: 17.0  
Sex: Female  
Location: Unknown  
Vaccinated:2015-12-01
Onset:2015-12-01
   Days after vaccination:0
Submitted: 2016-02-18
   Days after onset:79
Entered: 2016-02-26
   Days after submission:8
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MENB: MENINGOCOCCAL B (TRUMENBA) / PFIZER/WYETH - / 1 UN / IM

Administered by: Other       Purchased by: Other
Symptoms: Influenza like illness
SMQs:

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: No other medications
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2016023542

Write-up: This is a spontaneous report from a contactable physician through a Pfizer sales representative. A 17-year-old female patient of an unspecified ethnicity received first dose of TRUMENBA, intramuscular on unknown date in Dec2015 single dose. The patient medical history and the patient''s concomitant medications were not reported. The patient experienced flu like symptoms on Dec2015. The event lasted a couple of days then resolved. The event was assessed as non-serious.


VAERS ID: 625910 (history)  
Form: Version 1.0  
Age: 18.0  
Sex: Male  
Location: Kentucky  
Vaccinated:2015-11-09
Onset:0000-00-00
Submitted: 2016-02-18
Entered: 2016-02-26
   Days after submission:8
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR U1455AA / 5 UN / IM
MENB: MENINGOCOCCAL B (TRUMENBA) / PFIZER/WYETH J28923 / UNK LA / IM

Administered by: Other       Purchased by: Other
Symptoms: Vaccination complication
SMQs:

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: No other medications
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2016018413

Write-up: This is a spontaneous report from two contactable HCP communicated to a sales representative. The two HCP reported same event for 3 non-contactable unknown patients. This case is for the 3rd patient. A patient of unspecified age ethnicity and gender received TRUMENBA via an unspecified route of administration at 0.5ml, single on an unspecified date. The patient medical history was not reported. The patient''s concomitant medications were not reported. The patient experienced reaction to TRUMENBA on an unspecified date with outcome of unknown. The Pfizer sales representative mentioned that in the doctor''s opinion the reaction was due to TRUMENBA.


VAERS ID: 625912 (history)  
Form: Version 1.0  
Age: 20.0  
Sex: Female  
Location: New York  
Vaccinated:2015-05-21
Onset:2015-06-01
   Days after vaccination:11
Submitted: 2016-02-22
   Days after onset:266
Entered: 2016-02-26
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MENB: MENINGOCOCCAL B (TRUMENBA) / PFIZER/WYETH J28923 / 1 LA / IM

Administered by: Other       Purchased by: Other
Symptoms: Erythema, Fatigue, Pain, Peripheral swelling
SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), 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: ORTHO CYCLEN
Current Illness: Unknown
Preexisting Conditions: Coagulation factor VII level abnormal
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2016003525

Write-up: This is a spontaneous report from a contactable nurse and from a contactable physician. A 20-year-old female patient received first dose of TRUMENBA (Lot# J28923), intramuscular in left deltoid, on 21May2015, at 0.5 ml single. Relevant medical history included borderline factor 7 deficiency that did not require medications or treatments. Concomitant medication included ORTHO CYCLEN, oral, at 1 DF 1x/day, for oral contraception. The patient experienced really red swollen arm, about 4 inches swollen, a lot of pain and fatigue on Jun2015. The patient was treated with ice packs and TYLENOL either 650mg or 1000mg tablets by mouth 3 times a day as needed with good effect and relief. No other treatments were required. The events were assessed as non-serious. The events recovered. Follow-up (16Feb2016): New information received from a contactable physician includes: vaccination details. Follow-up attempts completed. No further information expected.


VAERS ID: 625914 (history)  
Form: Version 1.0  
Age: 11.0  
Sex: Male  
Location: Unknown  
Vaccinated:2016-01-18
Onset:2016-01-19
   Days after vaccination:1
Submitted: 2016-02-18
   Days after onset:30
Entered: 2016-02-26
   Days after submission:8
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. - / UNK LA / UN
MENB: MENINGOCOCCAL B (TRUMENBA) / PFIZER/WYETH M13066 / UNK RA / UN
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR - / UNK RA / UN
TTOX: TETANUS TOXOID (NO BRAND NAME) / UNKNOWN MANUFACTURER - / UNK UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Dizziness, Erythema, Fatigue, Headache, Pyrexia, Vomiting
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (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: No other medications
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2016048392

Write-up: This is a spontaneous report from a contactable physician via a Pfizer sales representative. A 11-year-old male patient received TRUMENBA (LOT M13066; NDC number 0005-0100-10; Expiry Date 30Sep2016), via an unspecified route of administration on 18Jan2016 at 0.5mL on right shoulder. The patient medical history was not reported. Concomitant medication included MENACTRA on right shoulder, HPV9 on left shoulder, tetanus vaccine, all given on 18Jan2016. On 19Jan2016 the patient experienced fatigue, dizziness, high fever 103.9 F, headache, red shoulder all the way to elbow and severe vomiting-threw up four times. Patient was treated with ZOFRAN given either 19Jan2016 or 20Jan2016 because patient kept throwing up and couldn''t keep TYLENOL down. All events recovered on 20Jan2016.


VAERS ID: 625915 (history)  
Form: Version 1.0  
Age: 20.0  
Sex: Female  
Location: Unknown  
Vaccinated:2015-12-28
Onset:0000-00-00
Submitted: 2016-02-18
Entered: 2016-02-26
   Days after submission:8
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MENB: MENINGOCOCCAL B (TRUMENBA) / PFIZER/WYETH - / 2 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Injection site erythema, Injection site pain, Injection site swelling, Injection site warmth
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (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: No other medications
Current Illness: Unknown
Preexisting Conditions: 08/2015, TRUMENBA, first dose
Allergies:
Diagnostic Lab Data:
CDC Split Type: 2016001274

Write-up: This is a spontaneous report from a contactable consumer. A 20-years-old female patient of an unspecified ethnicity received the second dose of TRUMENBA, via an unspecified route of administration on 28Dec2015 at single dose. The patient medical history and concomitant medications were not reported. The patient received the first dose of vaccine in Aug2015. The patient experienced warmth, redness, swelling of the injection site, and the site was tender all on an unspecified date with outcome of unknown.


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