Found 46977 events where Vaccine is FLU

VAERS ID: 331739   Vaccinated: 2008-10-21 Age: 21.0   Onset: 2008-10-26, Days after vaccination: 5 Gender: Male   Submitted: 2008-11-10, Days after onset: 15 Location: Unknown   Entered: 2008-11-10, Days after submission: 0	Life Threatening Illness? No Died? No Disability? No Recovered? Yes ER or Doctor Visit? Yes Hospitalized? No Current Illness: None Diagnostic Lab Data: ESR-wnl UA-wnl CBC-wnl Previous Vaccinations: rash~Influenza (Seasonal) (FluLaval)~1~21.00~In Patient Other Medications: None Preexisting Conditions: None CDC 'Split Type':
Vaccination Manufacturer Lot Dose Route Site FLU GLAXOSMITHKLINE BIOLOGICALS aflla177aa 0 IM UN
Administered by: Military     Purchased by: Unknown Symptoms: Abdominal pain, Arthralgia, Full blood count normal, Oedema peripheral, Red blood cell sedimentation rate normal, Skin lesion, Urine analysis normal Write-up: Abdominal and joint pain, swelling of hands x 1wk. Lesions noted on bilateral lower extremities. Tx'd with Prednisone 60mg x 3 days.
VAERS ID: 331766   Vaccinated: 2008-10-28 Age: 57.0   Onset: 2008-10-28, Days after vaccination: 0 Gender: Female   Submitted: 2008-11-05, Days after onset: 8 Location: New Hampshire   Entered: 2008-11-10, Days after submission: 5	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? Yes Hospitalized? No Current Illness: Unknown, but denied fever Diagnostic Lab Data: EKG; BW - results unknown Previous Vaccinations: Other Medications: Unknown Preexisting Conditions: Allergy to sulfa + hx multiple other allergies (unknown which ones) CDC 'Split Type':
Vaccination Manufacturer Lot Dose Route Site FLU SANOFI PASTEUR 02751AA   IM LA
Administered by: Other     Purchased by: Private Symptoms: Electrocardiogram, Feeling abnormal, Hypoaesthesia oral, Laboratory test, Lip swelling, Throat irritation Write-up: Approx. 4 1/2 hours after vaccine noted "Something wrong in throat". 7 hrs after vaccine "lips tripled, tongue felt as if recovering from Novocain". Following morning, lips still a little tirply and felt loopy". Went to ER -Rx with Nebulizer IM steroid
VAERS ID: 331769   Vaccinated: 2008-10-29 Age: 4.0   Onset: 2008-10-31, Days after vaccination: 2 Gender: Female   Submitted: 2008-11-06, Days after onset: 6 Location: Kentucky   Entered: 2008-11-10, Days after submission: 4	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? Yes Hospitalized? No Current Illness: Diagnostic Lab Data: None Previous Vaccinations: Other Medications: Preexisting Conditions: CDC 'Split Type':
Vaccination Manufacturer Lot Dose Route Site DTAP SANOFI PASTEUR U2356CA 4 IM RL FLU SANOFI PASTEUR U2811AA 1 IM LL IPV SANOFI PASTEUR A1060 4 SC RL MMR MERCK & CO. INC. 08914 1 IM LA
Administered by: Private     Purchased by: Public Symptoms: Hyperaemia, Injection site erythema, Injection site induration, Injection site pruritus, Injection site rash, Injection site warmth Write-up: Pt received 5th dose DTaP (TRIPEDIA from Sanofi) on (R) thigh on 10/29/08. Woke up on 10/31 (<48 hrs) with red, itchy, hot enlarging rash at the vaccine site, had 5x inches indurated, hyperemia all around the vaccination site. RTC BENADRYL, KEFLEX given cold/warm compress.
VAERS ID: 331772   Vaccinated: 2008-10-06 Age: 77.0   Onset: 2008-10-07, Days after vaccination: 1 Gender: Female   Submitted: 2008-11-09, Days after onset: 33 Location: Illinois   Entered: 2008-11-10, Days after submission: 1	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? No Hospitalized? No Current Illness: None Diagnostic Lab Data: None Previous Vaccinations: Other Medications: Atenolol, Dyazide Preexisting Conditions: Hypertension CDC 'Split Type':
Vaccination Manufacturer Lot Dose Route Site FLU SANOFI PASTEUR U2785HA 0 UN LA
Administered by: Other     Purchased by: Private Symptoms: Injected limb mobility decreased, Injection site pain Write-up: Severe soreness in left shoulder (injection site) resulting in inability to use arm (per patient). Suggested treatment over the counter with Ibuprofen, and a doctor visit, if no relief.
VAERS ID: 331776   Vaccinated: 2008-10-31 Age: 65.0   Onset: 2008-10-31, Days after vaccination: 0 Gender: Female   Submitted: 2008-11-07, Days after onset: 7 Location: Florida   Entered: 2008-11-10, Days after submission: 3	Life Threatening Illness? No Died? No Disability? No Recovered? Yes ER or Doctor Visit? Yes Hospitalized? No Current Illness: None Diagnostic Lab Data: None Previous Vaccinations: Other Medications: B/P Medication (name unknown) Preexisting Conditions: HTN CDC 'Split Type':
Vaccination Manufacturer Lot Dose Route Site FLU SANOFI PASTEUR U2771AA 0 IM LA
Administered by: Public     Purchased by: Private Symptoms: Swollen tongue, Throat tightness Write-up: Client received Influenza Virus vaccine at 12:00 pm 10/31/2008. Client returned to clinic-12:20pm 10/31/08 with c/o throat tightness and enlarged tongue upon exam, noted enlarged tongue. Pharynx open. Lungs CTA bilaterally no wheezing. Epipen 1:1000 .3mg given in L anterolateral thigh at 12:23 p.m.... Paramedics arrived at 12:25 p.m client reported felt better after Epipen. Client sent to ER via ambulance for further evaluation at 12:30 pm 10/31/2008.
VAERS ID: 331779   Vaccinated: 2008-11-04 Age: 55.0   Onset: 2008-11-04, Days after vaccination: 0 Gender: Female   Submitted: 0000-00-00 Location: Arizona   Entered: 2008-11-10	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: CLARITIN, PROZAC Preexisting Conditions: Intolerance to milk. CDC 'Split Type':
Vaccination Manufacturer Lot Dose Route Site FLU SANOFI PASTEUR U2809AA 0 IM LA PPV MERCK & CO. INC. 0990U 0 IM RA
Administered by: Unknown     Purchased by: Private Symptoms: Erythema, Lymphadenopathy, Urticaria Write-up: Hives, swollen glands, redness in lymph areas.
VAERS ID: 331780   Vaccinated: 2008-10-20 Age: 9.0   Onset: 2008-10-31, Days after vaccination: 11 Gender: Male   Submitted: 2008-10-31, Days after onset: 0 Location: New York   Entered: 2008-11-10, Days after submission: 10	Life Threatening Illness? No Died? No Disability? No Recovered? Yes ER or Doctor Visit? No Hospitalized? No Current Illness: Asthma Exacerbation Diagnostic Lab Data: Previous Vaccinations: Other Medications: Claritin, Albuterol Preexisting Conditions: CDC 'Split Type':
Vaccination Manufacturer Lot Dose Route Site FLU SANOFI PASTEUR U2790BA   UN LA
Administered by: Private     Purchased by: Unknown Symptoms: Urticaria Write-up: Hives occurring the next morning, treatment Benadryl 06hr pm. Was seen 11/3/08 hives were resolved by the next day.
VAERS ID: 331789   Vaccinated: 2008-10-20 Age: 46.0   Onset: 2008-10-21, Days after vaccination: 1 Gender: Female   Submitted: 2008-11-06, Days after onset: 16 Location: Utah   Entered: 2008-11-10, Days after submission: 4	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? Yes Hospitalized? No Current Illness: Diagnostic Lab Data: Not reported. Previous Vaccinations: Other Medications: Preexisting Conditions: History of Eustachian tube problems (not specified). CDC 'Split Type': 200803358
Vaccination Manufacturer Lot Dose Route Site FLU SANOFI PASTEUR     UN UN
Administered by: Unknown     Purchased by: Unknown Symptoms: Deafness unilateral, Sudden hearing loss Write-up: Initial report received from a health professional on 27 October 2008. A 46-year-old female patient had received a dose of FLUZONE SV 2008-2009 (lot number unknown; route and site of administration not reported) on 20 October 2008 and within 24 hours, she complained of sudden hearing loss in her right ear. The patient was seen by a physician on 22 October 2008. No additional details were provided. Documents held by sender: None
VAERS ID: 331790   Vaccinated: 2008-10-26 Age: 66.0   Onset: 2008-10-26, Days after vaccination: 0 Gender: Male   Submitted: 2008-11-06, Days after onset: 11 Location: Nevada   Entered: 2008-11-10, Days after submission: 4	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? Yes Hospitalized? No Current Illness: Diagnostic Lab Data: Not reported. Previous Vaccinations: Other Medications: PRILOSEC; UROXATRAL; glucosamine; vitamin B; AVODART Preexisting Conditions: Patient's past medical history included enlarged prostate, acid reflux, CIPRO allergies and NEOSPORIN antibiotic cream allergy. CDC 'Split Type': 200803361
Vaccination Manufacturer Lot Dose Route Site FLU SANOFI PASTEUR U2742A 9 IM LA
Administered by: Other     Purchased by: Other Symptoms: Chest discomfort, Cough, Dyspnoea, Eye discharge, Eye pain, Heart rate increased, Ocular hyperaemia, Speech disorder, Vaccine positive rechallenge, Vision blurred, Wheezing Write-up: Initial information was received on 28 October 2008 from a consumer. A 66 year old male patient with a history of enlarged prostate, acid reflux, allergies to CIPRO and NEOSPORIN antibiotic cream received an intramuscular left deltoid injection of FLUZONE (lot number U2742AA) on 26 October 2008 at 1:25 PM. The patient reported that he received FLUZONE on a yearly basis since 1999. He had similar symptoms in the past although the symptoms were not as severe. On 26 October 2008 at 5:30 PM the patient developed difficulty breathing, wheezing, coughing, couldn't talk and upper chest discomfort. At 6:30 PM the patient's eyes became gritty, white pus coming out of the eyes, eyes were blood shot and vision was blurred. At 7:30 PM his pulse was elevated. At 8:15 the patient was still wheezing but improved after he took BENADRYL. On 27 October 2008 his eyes were hurting and on 28 October 2008 his eyes were red. It was noted that the patient was seen by the paramedics but refused to go to the hospital. The patient was not recovered at the time of the report. List of Documents held by Sender: None.
VAERS ID: 331791   Vaccinated: 0000-00-00 Age: 79.0   Onset: 0000-00-00 Gender: Female   Submitted: 2008-11-06 Location: Virginia   Entered: 2008-11-10, Days after submission: 4	Life Threatening Illness? No Died? No Disability? No Recovered? No ER or Doctor Visit? Yes Hospitalized? No Current Illness: Diagnostic Lab Data: Not reported. Previous Vaccinations: Other Medications: Preexisting Conditions: Not reported. CDC 'Split Type': 200803365
Vaccination Manufacturer Lot Dose Route Site FLU UNKNOWN MANUFACTURER     UN UN
Administered by: Unknown     Purchased by: Unknown Symptoms: Aspiration pleural cavity, Chest X-ray abnormal, Chronic obstructive pulmonary disease, Dyspnoea, Ex-tobacco user, Pericarditis, Pleural effusion, Vaccination complication Write-up: Initial report received from another manufacturer on 29 October 2008 who received the report from a health care professional. A female patient (age not reported) developed reactive pericarditis after receiving an unspecified influenza vaccine. The date of the vaccine administration and the date of onset of symptoms were not specified. No additional details were reported. Documents held by sender: None 11/21/08 Reviewed Pulmo records received from CDC. FINAL DX: COPD Records reveal patient had been hospitalized 12/2002 w/pleural effusion secondary to flu shot & was seen in office 8/9/2003. Had thoracentesis in hospital that was non-diagnostic. Cardiac w/u neg. Had continued SOB. Ex-smoker who quit 12/2002. CXR c/w COPD. Tx w/inhalers.