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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126007041 | 12600704 | 1 | I | 20160718 | 20160727 | 20160727 | EXP | CA-FRI-1000086487 | FOREST | 34.00 | YR | F | Y | 84.00000 | KG | 20160727 | OT | DK | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126007041 | 12600704 | 1 | PS | ESCITALOPRAM | ESCITALOPRAM OXALATE | 1 | Unknown | U | 21323 | TABLET | |||||||||
| 126007041 | 12600704 | 2 | SS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | 9.5238 MG | U | 0 | 400 | MG | POWDER FOR SOLUTION FOR INJECTION | ||||||
| 126007041 | 12600704 | 3 | C | DICLECTIN | DOXYLAMINE SUCCINATEPYRIDOXINE HYDROCHLORIDE | 1 | Unknown | 0 | TABLET | ||||||||||
| 126007041 | 12600704 | 4 | C | ERGOCALCIFEROL. | ERGOCALCIFEROL | 1 | Unknown | 0 | |||||||||||
| 126007041 | 12600704 | 5 | C | PROGESTERONE. | PROGESTERONE | 1 | Unknown | 0 | |||||||||||
| 126007041 | 12600704 | 6 | C | VITAMIN B12 | CYANOCOBALAMIN | 1 | Other | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126007041 | 12600704 | 1 | Product used for unknown indication |
| 126007041 | 12600704 | 2 | Crohn's disease |
| 126007041 | 12600704 | 3 | Product used for unknown indication |
| 126007041 | 12600704 | 4 | Product used for unknown indication |
| 126007041 | 12600704 | 5 | Product used for unknown indication |
| 126007041 | 12600704 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126007041 | 12600704 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126007041 | 12600704 | Amniotic fluid volume decreased | |
| 126007041 | 12600704 | Drug hypersensitivity | |
| 126007041 | 12600704 | Exposure during pregnancy | |
| 126007041 | 12600704 | Gestational diabetes | |
| 126007041 | 12600704 | Gestational hypertension | |
| 126007041 | 12600704 | Haematochezia | |
| 126007041 | 12600704 | Mucous stools | |
| 126007041 | 12600704 | Nausea | |
| 126007041 | 12600704 | Sinusitis | |
| 126007041 | 12600704 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |