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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125873201 | 12587320 | 1 | I | 201602 | 20160719 | 20160725 | 20160725 | PER | US-APOTEX-2016AP009993 | APOTEX | 28.00 | YR | F | Y | 0.00000 | 20160725 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125873201 | 12587320 | 1 | PS | PAXIL | PAROXETINE HYDROCHLORIDE | 1 | Unknown | UNK, UNKNOWN | U | U | 20031 | TABLET | |||||||
| 125873201 | 12587320 | 2 | SS | WELLBUTRIN | BUPROPION HYDROCHLORIDE | 1 | Oral | 450 MG, 1D | N | U | 0 | 450 | MG | TABLET | |||||
| 125873201 | 12587320 | 3 | SS | WELLBUTRIN | BUPROPION HYDROCHLORIDE | 1 | Oral | 150 MG, 1D | N | U | 0 | 150 | MG | TABLET | QD | ||||
| 125873201 | 12587320 | 4 | SS | IMITREX | SUMATRIPTAN SUCCINATE | 1 | Unknown | UNK, UNKNOWN | U | U | 0 | ||||||||
| 125873201 | 12587320 | 5 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | 40 MG, 1 IN 2 WKS | 0 | 40 | MG | /wk | |||||||
| 125873201 | 12587320 | 6 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | 40 MG, WE | 0 | 40 | MG | /wk | |||||||
| 125873201 | 12587320 | 7 | C | APRISO | MESALAMINE | 1 | U | 0 | |||||||||||
| 125873201 | 12587320 | 8 | C | TYLENOL #3 (US) | 2 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125873201 | 12587320 | 1 | Product used for unknown indication |
| 125873201 | 12587320 | 2 | Depression |
| 125873201 | 12587320 | 3 | Weight decreased |
| 125873201 | 12587320 | 4 | Product used for unknown indication |
| 125873201 | 12587320 | 5 | Colitis ulcerative |
| 125873201 | 12587320 | 7 | Colitis ulcerative |
| 125873201 | 12587320 | 8 | Pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125873201 | 12587320 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125873201 | 12587320 | Confusional state | |
| 125873201 | 12587320 | Drug hypersensitivity | |
| 125873201 | 12587320 | Memory impairment | |
| 125873201 | 12587320 | Off label use | |
| 125873201 | 12587320 | Seizure |
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 |
|---|---|---|---|---|---|---|
| 125873201 | 12587320 | 2 | 201602 | 0 | ||
| 125873201 | 12587320 | 3 | 201603 | 0 | ||
| 125873201 | 12587320 | 5 | 201510 | 201601 | 0 | |
| 125873201 | 12587320 | 6 | 201601 | 0 |