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Found 46977 events where Vaccine is FLU

Event Details Report

This is page 3518 out of 4698

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VAERS ID:331854  Vaccinated:2008-11-06
Age:40.0  Onset:2008-11-06, Days after vaccination: 0
Gender:Female  Submitted:2008-11-10, Days after onset: 4
Location:Vermont  Entered:2008-11-10, Days after submission: 0
Life Threatening Illness? No
Died? No
Disability? No
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Current Illness: None
Diagnostic Lab Data: None
Previous Vaccinations:
Other Medications: None
Preexisting Conditions: None
CDC 'Split Type':
Vaccination
Manufacturer
Lot
Dose
Route
Site
FLUNOVARTIS VACCINES AND DIAGNOSTICS878770IMLA
Administered by: Other     Purchased by: Other
Symptoms: Injection site pain
Write-up: Pain in arm where the injection was given. Tx=Ibuprofen - one time 400mg. Hurt for 3 days.

VAERS ID:331855  Vaccinated:2008-10-30
Age:86.0  Onset:2008-10-30, Days after vaccination: 0
Gender:Female  Submitted:0000-00-00
Location:Indiana  Entered:2008-11-10
Life Threatening Illness? No
Died? No
Disability? No
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Current Illness: None
Diagnostic Lab Data: None
Previous Vaccinations:
Other Medications: PLAVIX; ASA; LOTRAL CAPTOPRIL; TOPROL XL; SIMVASTATIN;
Preexisting Conditions: None
CDC 'Split Type':
Vaccination
Manufacturer
Lot
Dose
Route
Site
FLUSANOFI PASTEURU2745AA IMLA
Administered by: Private     Purchased by: Private
Symptoms: Anxiety, Feeling abnormal, Flushing, Heart rate increased, Respiratory rate increased, Vomiting
Write-up: 3 pm 10/30/08 Sister phoned stating Pt does not feel good at all. States pt's face is very flushed, P-100, R-44 and feeling very anxious. Pt vomited. Denied SOB, wheezing, hives, paleness or dizziness. Pt advised per Dr to use TYLENOL and rest. May also take BENADRYL.

VAERS ID:331856  Vaccinated:2008-10-23
Age:8.0  Onset:2008-10-26, Days after vaccination: 3
Gender:  Submitted:0000-00-00
Location:Massachusetts  Entered:2008-11-10
Life Threatening Illness? No
Died? No
Disability? No
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Current Illness: No
Diagnostic Lab Data:
Previous Vaccinations:
Other Medications:
Preexisting Conditions: None
CDC 'Split Type':
Vaccination
Manufacturer
Lot
Dose
Route
Site
FLUSANOFI PASTEURU2831AA1IMRA
PPVMERCK & CO. INC.1679U0SCRA
Administered by: Private     Purchased by: Private
Symptoms: Injection site erythema, Injection site pain, Injection site swelling
Write-up: 10-23-08 Pt received Fluvax and PPV23 in RA -10-27-2008 seen for c/o 24 degree redness, swelling, tenderness @ injection site- recommend ice, diphenhydramine prn with effect. Given PPV23 because only received 2 doses PCV7- History asthma-

VAERS ID:331859  Vaccinated:2008-10-29
Age:50.0  Onset:2008-10-30, Days after vaccination: 1
Gender:Female  Submitted:2008-11-03, Days after onset: 4
Location:Georga  Entered:2008-11-10, Days after submission: 7
Life Threatening Illness? No
Died? No
Disability? No
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Current Illness: None
Diagnostic Lab Data: None
Previous Vaccinations:
Other Medications: None
Preexisting Conditions: None
CDC 'Split Type': GA09094
Vaccination
Manufacturer
Lot
Dose
Route
Site
FLUSANOFI PASTEURU2807AA0IMRA
Administered by: Public     Purchased by: Private
Symptoms: Contusion, Erythema, Local swelling, Pain, Skin warm, Tenderness
Write-up: pt. noticed are was bruised, tender to touch, it was reddish in color and swollen, warm to touch. Area was very painful.

VAERS ID:331866  Vaccinated:2008-10-16
Age:60.0  Onset:2008-10-17, Days after vaccination: 1
Gender:Male  Submitted:2008-11-05, Days after onset: 19
Location:D.C.  Entered:2008-11-10, Days after submission: 5
Life Threatening Illness? No
Died? No
Disability? No
Recovered? Yes
ER or Doctor Visit? Yes
Hospitalized? No
Current Illness: Cellulitis @ injection site
Diagnostic Lab Data: WBC on 10/18/2008 - 12.0, 86.4 segs ; WBC on 10/19/2008, 10.9, 79.0 segs; WBC 10/20/2008, 7.4, 72 segs
Previous Vaccinations:
Other Medications:
Preexisting Conditions: HTN; Seizure DIS; PUD - all -> Erythromycin and Chromotin
CDC 'Split Type': 2008001
Vaccination
Manufacturer
Lot
Dose
Route
Site
FLUSANOFI PASTEURU2752AA UNRA
PPVMERCK & CO. INC.080300UNRA
Administered by: Other     Purchased by: Other
Symptoms: Cellulitis, Neutrophil percentage increased, White blood cell count increased
Write-up: 10/18/2008 presented to ED with cellulitis arm, put on followed up in ED 10/19 and 10/20/08.

VAERS ID:331873  Vaccinated:2008-11-07
Age:19.0  Onset:2008-11-09, Days after vaccination: 2
Gender:Male  Submitted:2008-11-10, Days after onset: 1
Location:Mississippi  Entered:2008-11-10, Days after submission: 0
Life Threatening Illness? No
Died? No
Disability? No
Recovered? No
ER or Doctor Visit? No
Hospitalized? No
Current Illness: none
Diagnostic Lab Data:
Previous Vaccinations:
Other Medications: none
Preexisting Conditions: none
CDC 'Split Type':
Vaccination
Manufacturer
Lot
Dose
Route
Site
FLUUNKNOWN MANUFACTURER    
Administered by: Unknown     Purchased by: Unknown
Symptoms: Muscular weakness, Oropharyngeal pain, Pain, Pyrexia
Write-up: 102.4 Fever, Sore throat, aches and muscle weakness

VAERS ID:331874  Vaccinated:2008-10-10
Age:65.0  Onset:2008-10-14, Days after vaccination: 4
Gender:Female  Submitted:2008-11-10, Days after onset: 27
Location:Florida  Entered:2008-11-10, Days after submission: 0
Life Threatening Illness? No
Died? No
Disability? No
Recovered? No
ER or Doctor Visit? No
Hospitalized? No
Current Illness: Had symptoms of respiratory illness 1-2 weeks prior to vaccination.
Diagnostic Lab Data: None
Previous Vaccinations:
Other Medications: Lisinopril and Prevastat
Preexisting Conditions: Hypertension Hyperlipdemia
CDC 'Split Type':
Vaccination
Manufacturer
Lot
Dose
Route
Site
FLUSANOFI PASTEURU2789AA1IMLA
PPVMERCK & CO. INC.0224X0IMRA
Administered by: Public     Purchased by: Public
Symptoms: Condition aggravated, Cough, Pyrexia, Respiratory disorder, Rhinorrhoea
Write-up: Patient reports exacerbation of cough, increased mucus and respiratory symptoms with fever 4-5 days after influenza vaccine. Still has symptoms. Has not seen MD. Taking OTC cough syrup and Tylenol.

VAERS ID:331875  Vaccinated:2008-11-06
Age:46.0  Onset:2008-11-06, Days after vaccination: 0
Gender:Female  Submitted:2008-11-10, Days after onset: 4
Location:Minnesota  Entered:2008-11-10, Days after submission: 0
Life Threatening Illness? No
Died? No
Disability? No
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Current Illness:
Diagnostic Lab Data: none
Previous Vaccinations:
Other Medications:
Preexisting Conditions:
CDC 'Split Type':
Vaccination
Manufacturer
Lot
Dose
Route
Site
FLUUNKNOWN MANUFACTURER 1  
Administered by: Unknown     Purchased by: Unknown
Symptoms: Cough, Dyspnoea, Eye irritation, Eye pruritus, Headache, No reaction on previous exposure to drug, Ocular hyperaemia, Pain, Palpitations, Pyrexia, Respiratory tract congestion
Write-up: This healthy 46-year-old received a flu shot around 10:30 a.m. this morning. Around noon she developed a dry, hacky cough, mild headache and body aches. She took some cold medicine thereafter developing a feeling of palpitations and mild shortness of breath. Now at 5:30 p.m. those two symptoms have resolved, but she feels very achy, has very red, irritated, itchy eyes, a fever and congestion. She does note in retrospect that she did have some body aches this morning upon waking. No known exposures. No previous reaction to flu shots. No history of egg allergy or other comorbidities.

VAERS ID:331876  Vaccinated:2008-10-10
Age:65.0  Onset:2008-10-12, Days after vaccination: 2
Gender:Male  Submitted:2008-11-10, Days after onset: 29
Location:Florida  Entered:2008-11-10, Days after submission: 0
Life Threatening Illness? No
Died? No
Disability? No
Recovered? No
ER or Doctor Visit? No
Hospitalized? No
Current Illness: Recent Surgery
Diagnostic Lab Data: Had Melanoma removed from left posterior Shoulder 10/03/08.
Previous Vaccinations:
Other Medications: None
Preexisting Conditions: Hx colon CA, Melanoma
CDC 'Split Type':
Vaccination
Manufacturer
Lot
Dose
Route
Site
FLUSANOFI PASTEURU2789AA1IMRA
PPVMERCK & CO. INC.0224X0IMLA
Administered by: Military     Purchased by: Public
Symptoms: Condition aggravated, Cough, Influenza, Injection site pain, Pyrexia, Rhinorrhoea, Tenderness
Write-up: Client reports pain in left shoulder near injection site beginning 2 days after immunization. Pain and tenderness increased through 3rd and th day. Still has pain with certain movements and tendernees. Denies swelling,redness or induration. States feels like when he had a torn muscle. Took Tylenol. Also reprots exacerbation of "flu" symptoms, increase, cough, Mucus, slight fever 4-5 days after immunizations recieved.

VAERS ID:331879  Vaccinated:2008-10-20
Age:77.0  Onset:2008-10-20, Days after vaccination: 0
Gender:Female  Submitted:2008-11-10, Days after onset: 21
Location:South Carolina  Entered:2008-11-10, Days after submission: 0
Life Threatening Illness? No
Died? No
Disability? No
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 4 days
    Extended hospital stay? No
Current Illness: None
Diagnostic Lab Data: Unknown LABS: WBC 13.5, neutros 90.1%, lymphs 1%. Urine c/s (+) Klebsiella pneumonia.
Previous Vaccinations:
Other Medications: Unknown
Preexisting Conditions: Allergies: sulfa PMH: GERD, hiatal hernia, pancreatitis, gasteoenteritis, arthritis, CHF.
CDC 'Split Type': SC0815
Vaccination
Manufacturer
Lot
Dose
Route
Site
FLUSANOFI PASTEURU2765AA1IMLA
PPVMERCK & CO. INC.1679U IMLA
Administered by: Unknown     Purchased by: Unknown
Symptoms: Asthenia, Breast pain, Cellulitis, Culture urine positive, Dehydration, Fall, Gastroenteritis, Immediate post-injection reaction, Injection site erythema, Injection site pain, Injection site swelling, Injection site warmth, Klebsiella infection, Lymphocyte percentage decreased, Musculoskeletal pain, Nausea, Neutrophil percentage increased, Urinary tract infection, Vomiting, White blood cell count increased
Write-up: Received flu and pneumonia vaccine on 10/20/08. C/O pain in injection site (LA) immediately. Continued to be painful with radiation under arm to L breast area. Vomiting on 10/21/08--reported to ER on 10/21/08. Swelling, redness @ site. Patient requested both given in L arm. Patient has signed release of record form to get hospital records for further medical information regarding this incident. 11/18/08 Reviewed hospital medical records of 10/21-10/24/2008. FINAL DX: cellulitis left shoulder; right shoulder pain secondary to fall at home; & acute gastroenteritis w/dehydration Records reveal patient experienced nausea, vomiting & weakness x 2 days. Injection site edema, erythema, warmth & pain which extended into left anterior chest wall.

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