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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126206162 | 12620616 | 2 | F | 2000 | 20160720 | 20160804 | 20160804 | EXP | US-JNJFOC-20160719441 | JOHNSON AND JOHNSON | LARSON AM. ACETAMINOPHEN-INDUCED ACUTE LIVER FAILURE: RESULTS OF A UNITED STATES MULTICENTER, PROSPECTIVE STUDY. HEPATOLOGY 2005. | 52.00 | YR | A | F | Y | 122.00000 | KG | 20160804 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126206162 | 12620616 | 1 | PS | TYLENOL | ACETAMINOPHEN | 1 | Unknown | U | U | 19872 | UNSPECIFIED | ||||||||
| 126206162 | 12620616 | 2 | SS | TYLENOL | ACETAMINOPHEN | 1 | Unknown | TOTAL DOSE 84000MG, CHRONIC USE 21 DAYS (3 WEEEKS) | 84000 | MG | U | U | 19872 | 4000 | MG | UNSPECIFIED | |||
| 126206162 | 12620616 | 3 | SS | MACROBID | NITROFURANTOINNITROFURANTOIN MONOHYDRATE | 1 | Unknown | U | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126206162 | 12620616 | 2 | Arthralgia |
| 126206162 | 12620616 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126206162 | 12620616 | OT |
| 126206162 | 12620616 | HO |
| 126206162 | 12620616 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126206162 | 12620616 | Acute hepatic failure | |
| 126206162 | 12620616 | Chest X-ray abnormal | |
| 126206162 | 12620616 | Off label use | |
| 126206162 | 12620616 | Overdose | |
| 126206162 | 12620616 | Product use issue |
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 |
|---|---|---|---|---|---|---|
| 126206162 | 12620616 | 2 | 2000 | 0 |