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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125884601 | 12588460 | 1 | I | 20160620 | 20160725 | 20160725 | PER | US-JNJFOC-20160620312 | JANSSEN | 0.00 | Y | 77.11000 | KG | 20160725 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125884601 | 12588460 | 1 | PS | TYLENOL | ACETAMINOPHEN | 1 | Oral | U | U | 19872 | UNSPECIFIED | ||||||||
| 125884601 | 12588460 | 2 | SS | TYLENOL | ACETAMINOPHEN | 1 | Oral | U | U | 19872 | 1000 | MG | UNSPECIFIED | ||||||
| 125884601 | 12588460 | 3 | SS | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Oral | U | U | 999999 | 25 | MG | UNSPECIFIED | ||||||
| 125884601 | 12588460 | 4 | C | REMICADE | INFLIXIMAB | 1 | Oral | 0 | 400 | MG | LYOPHILIZED POWDER |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125884601 | 12588460 | 2 | Premedication |
| 125884601 | 12588460 | 3 | Premedication |
| 125884601 | 12588460 | 4 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125884601 | 12588460 | Off label use | |
| 125884601 | 12588460 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |