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From the 6/11/2021 release of VAERS data:

Found 239 cases where Symptom is Crohn's disease



Case Details

This is page 5 out of 24

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VAERS ID: 518542 (history)  
Form: Version 1.0  
Age: 22.0  
Sex: Female  
Location: Tennessee  
Vaccinated:2009-04-08
Onset:2010-06-01
   Days after vaccination:419
Submitted: 2014-01-06
   Days after onset:1315
Entered: 2014-01-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0548X / 3 - / UN

Administered by: Public       Purchased by: Private
Symptoms: Crohn's disease, Gastrointestinal haemorrhage, Laboratory test, Type 1 diabetes mellitus
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Hyperglycaemia/new onset diabetes mellitus (narrow), Gastrointestinal premalignant disorders (narrow), Gastrointestinal haemorrhage (narrow), Ischaemic colitis (broad), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? Yes
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: Crohn''s Disease~HPV (Gardasil)~UN~23.50~Patient
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data: Yes - I have medical records
CDC Split Type:

Write-up: I developed GI bleeding which grew worse over months. I was diagnosed with Crohn''s disease in July 2010. I was also diagnosed with Type 1 Diabetes in October 2010.


VAERS ID: 528307 (history)  
Form: Version 1.0  
Age: 20.0  
Sex: Male  
Location: California  
Vaccinated:2010-04-08
Onset:2010-04-09
   Days after vaccination:1
Submitted: 2014-04-14
   Days after onset:1466
Entered: 2014-04-14
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
ANTH: ANTHRAX (BIOTHRAX) / EMERGENT BIOSOLUTIONS FAV226 / 5 RA / SYR

Administered by: Military       Purchased by: Military
Symptoms: Abdominal pain, Aspartate aminotransferase increased, Blood test abnormal, Burning sensation, Colonoscopy abnormal, Crohn's disease, Hypersensitivity, Intestinal fistula, Local swelling, Musculoskeletal stiffness, Shock, Skin tightness, Swelling, Vaccination complication, Vaccination site inflammation
SMQs:, Liver related investigations, signs and symptoms (narrow), Anaphylactic reaction (narrow), Acute pancreatitis (broad), Angioedema (broad), Peripheral neuropathy (broad), Retroperitoneal fibrosis (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Hypovolaemic shock conditions (narrow), Toxic-septic shock conditions (narrow), Anaphylactic/anaphylactoid shock conditions (narrow), Hypoglycaemic and neurogenic shock conditions (narrow), Pseudomembranous colitis (broad), Gastrointestinal premalignant disorders (narrow), Dystonia (broad), Parkinson-like events (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Gastrointestinal perforation (narrow), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific inflammation (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Ischaemic colitis (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Arthritis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (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: Allergic reaction~Influenza (Seasonal) (no brand name)~~19.00~Patient|adverse reaction~Anthrax (Biothrax)~4~19.00~Patient|advers
Other Medications: Benadryl and Tylenol to counter side effects from the vaccination. That is all that can be remembered as far as additional medication.
Current Illness: N/A
Preexisting Conditions: Allergic to amoxicillin and previous adverse reaction to Anthrax booster #3 given on May 19, 2008 and booster #4 given on October 28, 2008. Just prior to booster #4, severe intestinal inflammation developed which would be diagnosed as Crohn''s disease in 2012. After surgical intervention the symptoms subsided until after reception of boosters 4 and 5.
Allergies:
Diagnostic Lab Data: In October 2012, a Prometheus test was ordered that did indicate that I had Crohn''s Disease with a colonoscopy in March 2013 to support the level of damage. I had several fistulas that are now beginning to close as I am on Remicade. My liver has high hepatic counts for amino and aspartate transphase numbers which prevents me from taking 6MP for Crohn''s.
CDC Split Type:

Write-up: Severe abdominal pains after booster #3 with swelling and tightness of the arm. Booster #4 left the vaccination site inflammed for several weeks and caused stiffness in the arm. Booster #5 caused immediate burning and swelling. Booster #5 caused me to enter shock which may have been due to an allergic reaction to the shot, or adverse effect. Previous shots had adverse reactions, but nothing was done. After #5 the facility annotated it and provided a permanent exemption from shot series.


VAERS ID: 528916 (history)  
Form: Version 1.0  
Age:   
Sex: Male  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2014-04-17
Entered: 2014-04-21
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
ANTH: ANTHRAX (BIOTHRAX) / EMERGENT BIOSOLUTIONS - / UNK UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Crohn's disease
SMQs:, Gastrointestinal premalignant disorders (narrow), Ischaemic colitis (broad), Immune-mediated/autoimmune disorders (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: Unknown. Sibling has Crohn''s disease.
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: 14AV00006SP

Write-up: On 14APR2014, information was received from a consumer on behalf of his brother. The reporter stated that his brother had received the Anthrax vaccine (date, dose, lot# not reported). On an unspecified date the male was diagnosed with Crohn''s disease. At the time of report, the Crohn''s disease was in remission. The reporter stated that there was no prior family history of Crohn''s disease. Reporter stated that the subject is in remission. Follow-up information has been requested.


VAERS ID: 528917 (history)  
Form: Version 1.0  
Age: 18.0  
Sex: Male  
Location: Texas  
Vaccinated:2008-04-11
Onset:0000-00-00
Submitted: 2014-04-17
Entered: 2014-04-21
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
ANTH: ANTHRAX (BIOTHRAX) / EMERGENT BIOSOLUTIONS - / 1 UN / UN
TYP: TYPHOID VI POLYSACCHARIDE (NO BRAND NAME) / UNKNOWN MANUFACTURER A02212 / UNK UN / UN

Administered by: Military       Purchased by: Military
Symptoms: Abdominal pain, Anal sphincterotomy, Convulsion, Crohn's disease, Fistula, Hepatic enzyme increased, Immediate post-injection reaction, Impaired work ability, Local swelling, Pain in extremity, Rectal fissure, Rectal haemorrhage, Respiratory arrest, Shock, Skin discolouration, Surgery, Tuberculin test
SMQs:, Liver related investigations, signs and symptoms (narrow), Anaphylactic reaction (narrow), Acute pancreatitis (broad), Angioedema (broad), Haemorrhage terms (excl laboratory terms) (narrow), Systemic lupus erythematosus (broad), Retroperitoneal fibrosis (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Hypovolaemic shock conditions (narrow), Toxic-septic shock conditions (narrow), Anaphylactic/anaphylactoid shock conditions (narrow), Hypoglycaemic and neurogenic shock conditions (narrow), Convulsions (narrow), Gastrointestinal premalignant disorders (narrow), Gastrointestinal haemorrhage (narrow), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Ischaemic colitis (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Hypersensitivity (narrow), Respiratory failure (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (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? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: No other medications
Current Illness: 06/15/2008, Chronic tonsillitis; 06/15/2008, Sleep apnoea syndrome
Preexisting Conditions: Hypersensitivity, "other reactions" to vaccines in the past
Allergies:
Diagnostic Lab Data: 11APR2008, Tuberculin Skin Test, PPD administered
CDC Split Type: 14AV00005SP

Write-up: Information was received on 10APR2014 from a consumer. A 19 year old male experienced Crohn''s disease and underwent a sphincterotomy, considered medically significant by the Sponsor. In 2008, the male received a primary dose of BIOTHRAX. Subsequently on unspecified dates, he received two additional doses of vaccine. He stated that the first two doses had been "conducted improperly, but the damage had already been done". Within two months of the second vaccination he reported the development of "symptoms of Crohn''s disease" and subsequently he underwent a sphincterotomy while out of the country. In OCT2012, he was officially diagnosed with Crohn''s disease. The related symptoms had been present from 2008 to current. The male stated that a "medical separation from full-time job" was pending due to the development of Crohn''s disease. Additional information was received from consumer on 14APR2014 in the form of immunization records and a data collection form. Within months of receiving his first three doses of Anthrax vaccine, the consumer reported that he noticed severe abdominal pain and rectal bleeding. The symptoms continued "until a medical doctor told me I had a fistula and several rectal fissures" which required surgical correction. In AUG2008, surgical correction was performed. His symptoms subsided until 28OCT2008. On 28OCT2008 the consumer received dose four of BIOTHRAX which caused swelling and localized pain to his arm as well as discoloration for several days. He stated that the reaction was reported, but "no action was taken". On 08APR2010 he received dose five of BIOTHRAX (Lot FAV226). Immediately upon receipt of the vaccine, he reportedly "went into shock" and "was unable to breathe and began convulsing". He reported treatment with BENADRYL and TYLENOL. He stated at that time it was suggested that "based on other reactions to vaccines in the past that he may be allergic to a component in the vaccine but this was dismissed" based on non-reaction to previous doses. The consumer reported that on an unspecified date he was hospitalized for one day. Additionally, he reported that he experienced high liver enzymes. At the time of report, he stated that he has been "unable to enter remission" despite treatment with REMICADE. The consumer believed the anthrax vaccination may have activated the Crohn''s disease which was not known to previously exist in his family. Medical history included chronic tonsillitis with obstructive sleep apnea (15JUN2008). Concomitant medications were not reported. Vaccination History: Anthrax vaccine: 11APR2008, 28APR2008, 19MAY2008, 28OCT2008, 08APR2010 (Lot FAV226). Typhoid vaccine: 11APR2008, 02SEP2009. Influenza Split vaccine: 18JAN2008, 31OCT2008, 02SEP2009. Influenza (SEAS w/preservatives): 10OCT2013. Influenza, Novel H1N1 09: 29JAN2010. Hepatitis A / B: 25JUL2007, 31AUG2007, 18JAN2008. Meningococcal: 25JUL2007. MMR: 25JUL2007. Polio: 31AUG2007. Tetanus, diphtheria, pertussis: 25JUL2007, 26MAY2009. Vaccine Exemptions Noted: Anthrax (medical permanent), Hepatitis B (medical immune), Hepatitis A (medical immune), Influenza (medical permanent), smallpox (medical permanent), and varicella (medical immune). Further information has been requested.


VAERS ID: 533897 (history)  
Form: Version 1.0  
Age: 24.0  
Sex: Female  
Location: Georgia  
Vaccinated:2014-06-04
Onset:2014-06-04
   Days after vaccination:0
Submitted: 2014-06-16
   Days after onset:12
Entered: 2014-06-16
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEP: HEP B (ENGERIX-B) / GLAXOSMITHKLINE BIOLOGICALS C9N3F / 4 LA / IM

Administered by: Private       Purchased by: Private
Symptoms: Abdominal pain upper, Asthenia, Crohn's disease, Diarrhoea, Fatigue, Hypoaesthesia, Impaired work ability, Malaise, Proctalgia, Rectal haemorrhage, Swelling
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (broad), Peripheral neuropathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Pseudomembranous colitis (broad), Gastrointestinal premalignant disorders (narrow), Gastrointestinal haemorrhage (narrow), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Ischaemic colitis (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Noninfectious diarrhoea (narrow), Immune-mediated/autoimmune disorders (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: Unknown
Current Illness: Unknown
Preexisting Conditions: Crohn''s disease that had been in remission for 5 years.
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: "The day I received the shot I had a general feeling of un-wellness. About 45 min after being given the shot the left side of my face began to go numb but subsided after about an hour." "My Crohn''s symptoms started 5 days after receiving the shot. My Crohn''s symptoms have not subsided yet but are not as severe as they were last week. I have been having severe stomach pain and diarrhea. I have also began having rectal pain, swelling and bleeding. These symptoms are common with my Crohns as it is mostly in what is left of my colon. I have also been experiencing severe fatigue. Exactly 5 days after I received the shot, I had to leave work due to weakness and fatigue. This is still affecting me some." I am having her contact our Nurse Triage line and get a referral to the clinic to be seen by an MD.


VAERS ID: 557780 (history)  
Form: Version 1.0  
Age: 1.0  
Sex: Female  
Location: Florida  
Vaccinated:2003-06-02
Onset:0000-00-00
Submitted: 2014-11-27
Entered: 2014-11-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. - / 3 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Crohn's disease, Hepatitis B antibody negative, Hepatitis B surface antibody negative, Weight gain poor
SMQs:, Gastrointestinal premalignant disorders (narrow), Ischaemic colitis (broad), Immune-mediated/autoimmune disorders (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:
Allergies:
Diagnostic Lab Data: 2014, patient had negative titers for Hepatitis B; 2014, Hepatitis B surface antibody, negative, negative titers N/A
CDC Split Type: WAES1411USA011043

Write-up: This spontaneous report as received from a consumer refers to her daughter, a female patient of unknown age. On 01-AUG-2002, 02-OCT-2002 and 02-JUN-2003 the patient received doses of RECOMBIVAXHB)(lot#, dose, route not reported) vaccine series. Concomitant medications included PENTASOL. The consumer reported that the patient was "recently", in appropriately 2014, found to have negative titers for Hepatitis B during a screening for initiation of treatment with immunomodulator drugs for treatment for what appears to be Crohn''s disease. The consumer reported that the patient was perfectly health her entire life until February 2014, she got a ''stomach bug,'' and it never went away." The consumer stated that, at 11 years old, the patient was "failing to gain weight," but she didn''t start to manifest any symptoms of Crohn''s disease until "this year", in 2014. Outcome of Crohn''s disease was reported as not recovered. Outcome of negative titers for Hepatitis B was unknown. Additional information has been requested.


VAERS ID: 580745 (history)  
Form: Version 1.0  
Age: 13.0  
Sex: Male  
Location: Washington  
Vaccinated:2015-01-21
Onset:2015-02-07
   Days after vaccination:17
Submitted: 2015-06-06
   Days after onset:118
Entered: 2015-06-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
FLUN4: INFLUENZA (SEASONAL) (FLUMIST QUADRIVALENT) / MEDIMMUNE VACCINES, INC. - / 1 NS / IN

Administered by: Unknown       Purchased by: Other
Symptoms: Abdominal pain upper, Crohn's disease, Decreased appetite, Inflammation, Pyrexia, Weight decreased
SMQs:, Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal premalignant disorders (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Ischaemic colitis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: No
Preexisting Conditions: No
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Not eating, losing weight, severe stomach pain, fever, the inflammation caused Crohn''s disease. He has never had any symptoms prior to the vaccine.


VAERS ID: 589662 (history)  
Form: Version 1.0  
Age: 13.0  
Sex: Male  
Location: Unknown  
Vaccinated:2012-07-30
Onset:2013-03-01
   Days after vaccination:214
Submitted: 2015-08-06
   Days after onset:887
Entered: 2015-08-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. H009745 / 1 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Crohn's disease, Inappropriate schedule of drug administration
SMQs:, Gastrointestinal premalignant disorders (narrow), Ischaemic colitis (broad), Medication errors (narrow), Immune-mediated/autoimmune disorders (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: Seasonal allergy; Scoliosis
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: WAES1508USA002412

Write-up: This spontaneous report as received from a registered nurse refers to a 13 year old male patient. The patient''s medical history and concomitant medications were not reported. His concurrent conditions included an idiopathic scoliosis and unspecified seasonal allergies. On 30-JUL-2012, the patient was vaccinated with the first dose of GARDASIL 9 (expiration date 11-JAN-2015, lot # reported as H009745; dose and route of administration were not reported). In March 2013, the patient was diagnosed with Crohn''s disease. The patient sought an unspecified type of medical attention and he received the treatment with REMICADE (it was also reported as concomitant medication). On 31-JUL-2013, the patient was vaccinated with the second dose of GARDASIL 9 (expiration date 07-JAN-2015, lot # reported as J003727; dose and route of administration were not reported). On 05-AUG-2015, the patient was vaccinated with the third dose of GARDASIL 9 (expiration date 10-MAY-2017, lot # reported as K016966; dose and route of administration were not reported). The outcome of Crohn''s disease was unknown. The relatedness between the adverse event and the vaccination with GARDASIL 9 was not reported. Additional information has been requested.


VAERS ID: 597678 (history)  
Form: Version 1.0  
Age: 60.0  
Sex: Female  
Location: Washington  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2015-09-29
Entered: 2015-09-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. - / UNK UN / SC

Administered by: Other       Purchased by: Other
Symptoms: Condition aggravated, Crohn's disease
SMQs:, Gastrointestinal premalignant disorders (narrow), Ischaemic colitis (broad), Immune-mediated/autoimmune disorders (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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: HUMIRA; Prednisone
Current Illness: Crohn''s disease, medical history with Crohn''s disease in the past prior to the vaccination
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: WAES1509USA013806

Write-up: This spontaneous report as received from a physician via company representative refers to a 60 year old female patient. The patient had a medical history with Crohn''s disease in the past prior to the vaccination. The patient''s drug reactions or allergies were not reported. On an unknown date, the patient was vaccinated subcutaneously with ZOSTAVAX (dose, lot number and expiration date were not reported). Concomitant therapies included HUMIRA and prednisone (manufacturer unknown). On an unknown date, shortly after receiving the injection, the patient presented at a local hospital with unspecified symptoms and was admitted. She was diagnosed with Crohn''s disease (date not reported). The outcome of the event was not reported. The relatedness between the event and the ZOSTAVAX was not reported. Additional information has been requested.


VAERS ID: 615672 (history)  
Form: Version 1.0  
Age: 22.0  
Sex: Male  
Location: Pennsylvania  
Vaccinated:2014-09-12
Onset:2014-09-13
   Days after vaccination:1
Submitted: 2015-12-20
   Days after onset:463
Entered: 2015-12-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
FLUN4: INFLUENZA (SEASONAL) (FLUMIST QUADRIVALENT) / MEDIMMUNE VACCINES, INC. CF2251 / UNK NS / IN

Administered by: Military       Purchased by: Military
Symptoms: Abdominal X-ray, Abdominal pain, Colonoscopy normal, Computerised tomogram abnormal, Crohn's disease, Intestinal dilatation, Laboratory test normal, Nausea, Pathology test, Respiratory tract congestion, Small intestinal obstruction, Small intestinal resection, Ultrasound scan normal, Vomiting, Weight decreased, X-ray abnormal
SMQs:, Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Retroperitoneal fibrosis (broad), Gastrointestinal premalignant disorders (narrow), Malignancy related therapeutic and diagnostic procedures (narrow), Gastrointestinal obstruction (narrow), Gastrointestinal nonspecific dysfunction (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Ischaemic colitis (broad), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 8 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Possibly Motrin
Current Illness: None
Preexisting Conditions: No allergies; no birth defects; no medical conditions. Only history of illness was 2005-7 with e.histolytica parasite infection.
Allergies:
Diagnostic Lab Data: Nov 2014 and Dec 2014 abdominal xrays and CT scans identified SB dilation and obstruction. Normal labs. Normal Colonoscopy. March 2015 SB resection surgery. Pathology report consistent with Crohn''s disease.
CDC Split Type:

Write-up: Gradual onset of abdominal pain, nausea, vomiting and congestion. Sept 2014 abdominal xrays (2) and ultrasound were normal. Labs normal. Symptoms progressed in frequency and intensity. 15-20% weight loss. Hospitalization in Nov 2014 and Dec 2014. Xray and CT Scans identified SB dilation with possible SB obstruction. Obstruction not responsive to medical therapies to include high dose prednisone. March 2015 SB resection surgery, approx. 30 cm.


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