Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123472294 | 12347229 | 4 | F | 2016 | 20160902 | 20160509 | 20160906 | EXP | CA-PFIZER INC-2016243994 | PFIZER | 32.00 | YR | F | Y | 0.00000 | 20160906 | MD | CA | CA |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123472294 | 12347229 | 1 | PS | Pantoloc | PANTOPRAZOLE SODIUM | 1 | Oral | UNK, QD | 20987 | PROLONGED-RELEASE TABLET | |||||||||
| 123472294 | 12347229 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | 2.5 MG, 1/WEEK | U | 11719 | 2.5 | MG | TABLET | /wk | |||||
| 123472294 | 12347229 | 3 | SS | ENTYVIO | VEDOLIZUMAB | 1 | Intravenous (not otherwise specified) | 300 MG, UNK | 0 | 300 | MG | POWDER FOR SOLUTION FOR INFUSION | |||||||
| 123472294 | 12347229 | 4 | C | PREDNISONE. | PREDNISONE | 1 | UNK | 0 | |||||||||||
| 123472294 | 12347229 | 5 | C | NUVARING | ETHINYL ESTRADIOLETONOGESTREL | 1 | UNK | 0 | |||||||||||
| 123472294 | 12347229 | 6 | C | SALOFALK /00000301/ | MESALAMINE | 1 | UNK | 0 | |||||||||||
| 123472294 | 12347229 | 7 | C | CALCIUM VITAMIN D | CALCIUMVITAMIN D | 1 | UNK | 0 | |||||||||||
| 123472294 | 12347229 | 8 | C | CIPRALEX | ESCITALOPRAM OXALATE | 1 | UNK | 0 | |||||||||||
| 123472294 | 12347229 | 9 | C | DICYCLOMINE HYDROCHLORIDE. | DICYCLOMINE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 123472294 | 12347229 | 10 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123472294 | 12347229 | 3 | Colitis ulcerative |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123472294 | 12347229 | OT |
| 123472294 | 12347229 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123472294 | 12347229 | Abdominal pain | |
| 123472294 | 12347229 | Asthenia | |
| 123472294 | 12347229 | Cough | |
| 123472294 | 12347229 | Diarrhoea | |
| 123472294 | 12347229 | Fatigue | |
| 123472294 | 12347229 | Haematemesis | |
| 123472294 | 12347229 | Hypothermia | |
| 123472294 | 12347229 | Immunology test abnormal | |
| 123472294 | 12347229 | Neck pain | |
| 123472294 | 12347229 | Oropharyngeal pain | |
| 123472294 | 12347229 | Paraesthesia | |
| 123472294 | 12347229 | Tremor | |
| 123472294 | 12347229 | Viral infection |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 123472294 | 12347229 | 3 | 20151001 | 0 |